Takes of Marine Mammals Incidental to Specified Activities; U.S. Navy Training Activities in the Gulf of Alaska Temporary Maritime Activities Area, 9949-10023 [2016-03622]
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Vol. 81
Friday,
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February 26, 2016
Part II
Department of Commerce
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National Oceanic and Atmospheric Administration
50 CFR Part 218
Takes of Marine Mammals Incidental to Specified Activities; U.S. Navy
Training Activities in the Gulf of Alaska Temporary Maritime Activities Area;
Proposed Rule
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Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Proposed Rules
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 218
[Docket No. 141125997–6058–01]
RIN 0648–BE67
Takes of Marine Mammals Incidental to
Specified Activities; U.S. Navy Training
Activities in the Gulf of Alaska
Temporary Maritime Activities Area
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed rule; request for
comments and information.
AGENCY:
NMFS has received a request
from the U.S. Navy (Navy) for
authorization to take marine mammals
incidental to the training activities
conducted in the Gulf of Alaska (GOA)
Temporary Maritime Activities Area
(TMAA) Study Area (hereafter referred
to the Study Area) from May 2016
through May 2021. Pursuant to the
Marine Mammal Protection Act
(MMPA), NMFS is requesting comments
on its proposal to issue regulations and
subsequent Letter of Authorization
(LOA) to the Navy to incidentally harass
marine mammals.
DATES: Comments and information must
be received no later than March 28,
2016.
ADDRESSES: You may submit comments,
identified by NOAA–NMFS–2016–0008,
by any of the following methods:
• Electronic submissions: submit all
electronic public comments via the
Federal eRulemaking Portal, Go to
www.regulations.gov/
#!docketDetail;D=NOAA-NMFS-20160008, click the ‘‘Comment Now!’’ icon,
complete the required fields, and enter
or attach your comments.
• Mail: Submit comments to Jolie
Harrison, Chief, Permits and
Conservation Division, Office of
Protected Resources, National Marine
Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910–
3225.
• Fax: (301) 713–0376; Attn: Jolie
Harrison.
Instructions: Comments sent by any
other method, to any other address or
individual, or received after the end of
the comment period, may not be
considered by NMFS. All comments
received are a part of the public record
and will generally be posted for public
viewing on www.regulations.gov
without change. All personal identifying
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SUMMARY:
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information (e.g., name, address, etc.),
confidential business information, or
otherwise sensitive information
submitted voluntarily by the sender will
be publicly accessible. NMFS will
accept anonymous comments (enter
‘‘N/A’’ in the required fields if you wish
to remain anonymous). Attachments to
electronic comments will be accepted in
Microsoft Word, Excel, or Adobe PDF
file formats only.
FOR FURTHER INFORMATION CONTACT: John
Fiorentino, Office of Protected
Resources, NMFS, (301) 427–8477.
SUPPLEMENTARY INFORMATION:
Availability
A copy of the Navy’s LOA
application, which contains a list of the
references used in this proposed rule,
may be obtained by visiting the internet
at: https://www.nmfs.noaa.gov/pr/
permits/incidental/military.htm. The
Navy is preparing a Supplemental
Environmental Impact Statement (SEIS)/
Overseas EIS (OEIS) for the GOA TMAA
Study Area to evaluate all components
of the proposed training activities. The
Navy previously analyzed training
activities in the Study Area in the 2011
GOA Navy Training Activities FEIS
(GOA FEIS/OEIS) (U.S. Department of
the Navy, 2011a). The GOA Draft
Supplemental EIS (DSEIS)/OEIS was
released to the public on August 23,
2014, for review until October 22, 2014.
The Navy is the lead agency for the
GOA SEIS/OEIS, and NMFS is a
cooperating agency pursuant to 40 CFR
1501.6 and 1508.5. The GOA DSEIS/
OEIS, which also contains a list of the
references used in this proposed rule,
may be viewed at: https://
www.goaeis.com. Documents cited in
this notice may also be viewed, by
appointment, during regular business
hours, at the aforementioned address.
Background
Sections 101(a)(5)(A) and (D) of the
MMPA (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce to allow,
upon request, the incidental, but not
intentional, taking of small numbers of
marine mammals by U.S. citizens who
engage in a specified activity (other than
commercial fishing) within a specified
geographical region if certain findings
are made and either regulations are
issued or, if the taking is limited to
harassment, a notice of a proposed
authorization is provided to the public
for review.
Authorization for incidental takings
shall be granted if NMFS finds that the
taking will have a negligible impact on
the species or stock(s), will not have an
unmitigable adverse impact on the
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availability of the species or stock(s) for
subsistence uses (where relevant), and if
the permissible methods of taking and
requirements pertaining to the
mitigation, monitoring, and reporting of
such takings are set forth. NMFS has
defined ‘‘negligible impact’’ in 50 CFR
216.103 as ‘‘an impact resulting from
the specified activity that cannot be
reasonably expected to, and is not
reasonably likely to, adversely affect the
species or stock through effects on
annual rates of recruitment or survival.’’
The National Defense Authorization
Act of 2004 (NDAA) (Pub. L. 108–136)
removed the ‘‘small numbers’’ and
‘‘specified geographical region’’
limitations indicated above and
amended the definition of ‘‘harassment’’
as applies to a ‘‘military readiness
activity’’ to read as follows (section
3(18)(B) of the MMPA, 16 U.S.C.
1362(18)(B)): ‘‘(i) any act that injures or
has the significant potential to injure a
marine mammal or marine mammal
stock in the wild’’ [Level A
Harassment]; or ‘‘(ii) any act that
disturbs or is likely to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of natural
behavioral patterns, including, but not
limited to, migration, surfacing, nursing,
breeding, feeding, or sheltering, to a
point where such behavioral patterns
are abandoned or significantly altered’’
[Level B Harassment].
Summary of Request
On July 28, 2014, NMFS received an
application from the Navy requesting a
LOA for the take of 19 species of marine
mammals incidental to Navy training
activities to be conducted in the Study
Area over 5 years. On October 14, 2014,
the Navy submitted a revised LOA
application to reflect minor changes in
the number and types of training
activities. To address minor
inconsistencies with the DSEIS, the
Navy submitted a final revision to the
LOA application (hereafter referred to as
the LOA application) on January 21,
2015.
The Navy is requesting a 5-year LOA
for training activities to be conducted
from 2016 through 2021. The Study
Area is a polygon roughly the shape of
a 300 nm by 150 nm rectangle oriented
northwest to southeast in the long
direction, located south of Prince
William Sound and east of Kodiak
Island, Alaska (see Figure 1–1 of the
LOA application for a map of the Study
Area). The activities conducted within
the Study Area are classified as military
readiness activities. The Navy states that
these activities may expose some of the
marine mammals present within the
Study Area to sound from underwater
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acoustic sources and explosives. The
Navy requests authorization to take 19
marine mammal species by Level B
(behavioral) harassment; one of those
marine mammal species (Dall’s
porpoise) may be taken by Level A
(injury) harassment. The Navy is not
requesting mortality takes for any
species.
The LOA application and the GOA
DSEIS/OEIS contain acoustic thresholds
that, in some instances, represent
changes from what NMFS has used to
evaluate the Navy’s activities for
previous authorizations. The revised
thresholds, which the Navy developed
in coordination with NMFS, are based
on the evaluation and inclusion of new
information from recent scientific
studies; a detailed explanation of how
they were derived is provided in the
GOA DSEIS/OEIS Criteria and
Thresholds for U.S. Navy Acoustic and
Explosive Effects Analysis Technical
Report (available at https://
www.goaeis.com). The revised
thresholds are adopted for this proposed
rulemaking.
NOAA is currently in the process of
developing Acoustic Guidance on
thresholds for onset of auditory impacts
from exposure to sound, which will be
used to support assessments of the
effects of anthropogenic sound on
marine mammals. To develop this
Guidance, NOAA is compiling,
interpreting, and synthesizing the best
information currently available on the
effects of anthropogenic sound on
marine mammals, and is committed to
finalizing the Guidance through a
systematic, transparent process that
involves internal review, external peer
review, and public comment.
In December 2013, NOAA released for
public comment a ‘‘Draft Guidance for
Assessing the Effects of Anthropogenic
Sound on Marine Mammals: Acoustic
Threshold Levels for Onset of
Permanent and Temporary Threshold
Shifts’’ (78 FR 78822) (the term
‘‘threshold shift’’ refers to noise-induced
hearing loss). The Draft Guidance was
generally consistent with the Navy’s
Permanent Threshold Shifts/Temporary
Threshold Shifts (PTS/TTS) criteria
used in the GOA DSEIS/OEIS and
detailed within Finneran and Jenkins
(2012). Prior to the finalization of this
guidance by NOAA, the Navy suggested
revisions to the criteria (e.g., auditory
weighting functions and PTS/TTS
thresholds) based on a number of
studies available since the Navy’s Phase
2 modeling (the acoustic effects
modeling currently employed by the
Navy for training and testing activities),
including Finneran et al. (2005),
Finneran et al. (2010), Finneran and
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Schlundt (2013), Kastelein et al.
(2012a), Kastelein et al. (2012b),
Kastelein et al. (2014a), Kastelein et al.
(2014b), Popov et al. (2013), and Popov
et al. (2011). In January 2015, the Navy
submitted a draft proposal (Finneran
2015) to NOAA staff for their
consideration.
Finneran (2015) proposed new
weighting functions and thresholds for
predicting PTS/TTS in marine
mammals. The methodologies presented
within this paper build upon the
methodologies used to develop the
criteria applied within the Navy’s GOA
DSEIS/OEIS (Finneran and Jenkins,
2012) and incorporate relevant auditory
research made available since 2012.
While Finneran and Jenkins (2012)
presented a conservative approach to
development of auditory weighting
functions where data was limited,
Finneran (2015) synthesizes a wide
range of auditory data, including newly
available studies, to predict refined
auditory weighting functions and
corresponding TTS thresholds across
the complete hearing ranges of
functional hearing groups.
During the development process of
NOAA’s Draft Guidance, NOAA
incorporated Finneran (2015) into its
Draft Guidance. As a result, the Navy’s
proposal (Finneran, 2015) was
submitted for peer review by external
subject matter experts, in accordance
with the process previously conducted
for NOAA’s Draft Guidance. Peer review
comments were received by NOAA in
April 2015. NOAA subsequently
developed a Peer Review Report, which
was published on its Web site on July
31, 2015. The published report
documents the Navy’s proposal
(Finneran, 2015) that underwent peer
review, the peer-review comments, and
NOAA’s responses to those comments.
NOAA then incorporated this
information into revised Draft Guidance
which was published in the Federal
Register for public review and comment
(80 FR 45642) on July 31, 2015. The
auditory weighting functions and PTS/
TTS thresholds provided in that revised
Draft Guidance will not be adopted by
NOAA or applied to applicants until
Final Guidance is issued. At the time of
this proposed rulemaking, Final
Guidance has not been issued.
Therefore, the Navy has not adopted
these proposed criteria in its GOA
DSEIS/OEIS. However, the underlying
science contained within Finneran
(2015) has been addressed qualitatively
within the applicable sections of the
GOA DSEIS/OEIS and this rulemaking.
If the proposed criteria in Finneran
(2015) were adopted by NOAA,
incorporated into its Final Guidance,
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and applied to the Navy in the future,
predicted numbers of PTS/TTS would
change for most functional hearing
groups. However, because Finneran
(2015) relies on much of the same data
as the auditory criteria presented in the
Navy’s GOA DSEIS/OEIS, these changes
would not be substantial, and in most
cases would result in a reduction in the
predicted impacts. Predicted PTS/TTS
would be reduced over much to all of
their hearing range for low-frequency
cetaceans and phocids. Predicted PTS/
TTS for mid-frequency and highfrequency cetaceans would be reduced
for sources with frequencies below
about 3.5 kHz and remain relatively
unchanged for sounds above this
frequency. Predicted auditory effects on
otariids would increase for frequencies
between about 1 kHz and 20 kHz and
decrease for frequencies above and
below these points, although otariids
remain the marine mammals with the
least sensitivity to potential PTS/TTS.
Overall, predicted auditory effects
within this rulemaking would not
change significantly.
In summary, NOAA’s continuing
evaluation of all available science for
the Acoustic Guidance could result in
changes to the acoustic criteria used to
model the Navy’s activities for this
rulemaking, and, consequently, the
enumerations of ‘‘take’’ estimates.
However, at this time, the results of
prior Navy modeling described in this
notice represent the best available
estimate of the number and type of take
that may result from the Navy’s use of
acoustic sources in the GOA Study
Area. Further, consideration of the
revised Draft Guidance and information
contained in Finneran (2015) does not
alter our assessment of the likely
responses of marine mammals to
acoustic sources employed by Navy in
the GOA Study Area, or the likely
fitness consequences of those responses.
Finally, while acoustic criteria may also
inform mitigation and monitoring
decisions, this rulemaking requires a
robust adaptive management program
that regularly addresses new
information and allows for modification
of mitigation and/or monitoring
measures as appropriate.
Background of Request
The Navy’s mission is to organize,
train, equip, and maintain combat-ready
naval forces capable of winning wars,
deterring aggression, and maintaining
freedom of the seas. This mission is
mandated by federal law (10 U.S.C.
5062), which ensures the readiness of
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the naval forces of the United States.1
The Navy executes this responsibility by
establishing and executing training
programs, including at-sea training and
exercises, and ensuring naval forces
have access to the ranges, operating
areas (OPAREAs), and airspace needed
to develop and maintain skills for
conducting naval activities.
The Navy proposes to continue
conducting training activities within the
Study Area, which have been ongoing
since the 1990s. The tempo and types of
training activities have fluctuated
because of the introduction of new
technologies, the evolving nature of
international events, advances in war
fighting doctrine and procedures, and
force structure (organization of ships,
submarines, aircraft, weapons, and
personnel) changes. Such developments
influence the frequency, duration,
intensity, and location of required
training activities.
The Navy’s LOA request covers
training activities that would occur for
a 5-year period following the expiration
of the current MMPA authorization for
the GOA TMAA, which expires in 2016.
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Description of the Specified Activity
The Navy is requesting authorization
to take marine mammals incidental to
conducting training activities. The Navy
has determined that sonar use and
underwater detonations are the stressors
most likely to result in impacts on
marine mammals that could rise to the
level of harassment. Detailed
descriptions of these activities are
provided in the DSEIS/OEIS and in the
LOA application (https://
www.nmfs.noaa.gov/pr/permits/
incidental/military.htm) and are
summarized here.
Overview of Training Activities
The Navy routinely trains in the
Study Area in preparation for national
defense missions. Training activities
and exercises covered in the Navy’s
LOA request are briefly described
below, and in more detail within
chapter 2 of the GOA DSEIS/OEIS. Each
military training activity described
meets a requirement that can be traced
ultimately to requirements set forth by
the National Command Authority.2
The Navy categorizes training
activities into eight functional warfare
areas called primary mission areas: antiair warfare; amphibious warfare; strike
1 Title
10, Section 5062 of the U.S.C.
Command Authority’’ is a term used
by the United States military and government to
refer to the ultimate lawful source of military
orders. The term refers collectively to the President
of the United States (as commander-in-chief) and
the United States Secretary of Defense.
2 ‘‘National
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warfare; anti-surface warfare (ASUW);
anti-submarine warfare (ASW);
electronic warfare; mine warfare (MIW);
and naval special warfare (NSW). Most
training activities are categorized under
one of these primary mission areas;
those activities that do not fall within
one of these areas are in a separate
‘‘other’’ category. Each warfare
community (surface, subsurface,
aviation, and special warfare) may train
within some or all of these primary
mission areas. However, not all primary
mission areas are conducted within the
Study Area.
The Navy described and analyzed the
effects of its training activities within
the GOA DSEIS/OEIS. In its assessment,
the Navy concluded that of the activities
conducted within the Study Area, sonar
use and underwater detonations were
the stressors resulting in impacts on
marine mammals that could rise to the
level of harassment as defined under the
MMPA. Therefore, the LOA application
provides the Navy’s assessment of
potential effects from these stressors.
The specific acoustic sources used in
the LOA application are contained in
the GOA DSEIS/OEIS and are presented
in the following sections based on the
primary mission areas.
Anti-Surface Warfare (ASUW)
The mission of ASUW is to defend
against enemy ships or boats. In the
conduct of ASUW, aircraft use cannons,
air-launched cruise missiles or other
precision-guided munitions; ships
employ torpedoes, naval guns, and
surface-to-surface (S–S) missiles; and
submarines attack surface ships using
torpedoes or submarine-launched, antiship cruise missiles.
Anti-surface warfare training in the
Study Area includes S–S gunnery and
missile exercises (GUNEX and
MISSILEX) and air-to-surface (A–S)
bombing exercises (BOMBEX), GUNEX,
and MISSILEX. Also included in this
mission area is a sinking exercise that
may include S–S and A–S components.
Anti-Submarine Warfare (ASW)
The mission of ASW is to locate,
neutralize, and defeat hostile submarine
threats to surface forces. ASW is based
on the principle of a layered defense of
surveillance and attack aircraft, ships,
and submarines all searching for hostile
submarines. These forces operate
together or independently to gain early
warning and detection, and to localize,
track, target, and attack hostile
submarine threats.
Anti-submarine warfare training
addresses basic skills such as detection
and classification of submarines,
distinguishing between sounds made by
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enemy submarines and those of friendly
submarines, ships, and marine life.
ASW training evaluates the ability of
fleet assets to use systems, for example,
active and passive sonar and torpedo
systems to counter hostile submarine
threats. More advanced, integrated ASW
training exercises are conducted in
coordinated, at-sea training events
involving submarines, ships, and
aircraft. This training integrates the full
spectrum of ASW from detecting and
tracking a submarine to attacking a
target using simulated weapons.
Description of Sonar, Ordnance,
Targets, and Other Systems
The Navy uses a variety of sensors,
platforms, weapons, and other devices
to meet its mission. Training with these
systems and devices may introduce
acoustic (sound) energy into the
environment. The Navy’s current LOA
application describes underwater sound
as one of two types: impulsive and nonimpulsive. Sonar and similar sound
producing systems are categorized as
non-impulsive sound sources.
Underwater detonations of explosives
and other percussive events are
impulsive sounds.
Sonar and Other Active Acoustic
Sources
Modern sonar technology includes a
variety of sonar sensor and processing
systems. In concept, the simplest active
sonar emits sound waves, or ‘‘pings,’’
sent out in multiple directions, and the
sound waves then reflect off of the target
object in multiple directions. The sonar
source calculates the time it takes for
the reflected sound waves to return; this
calculation determines the distance to
the target object. More sophisticated
active sonar systems emit a ping and
then rapidly scan or listen to the sound
waves in a specific area. This provides
both distance to the target and
directional information. Even more
advanced sonar systems use multiple
receivers to listen to echoes from several
directions simultaneously and provide
efficient detection of both direction and
distance. Active sonar is rarely used
continuously throughout the listed
activities. In general, when sonar is in
use, the sonar ‘pings’ occur at intervals,
referred to as a duty cycle, and the
signals themselves are very short in
duration. For example, sonar that emits
a 1-second ping every 10 seconds has a
10 percent duty cycle. The Navy’s
largest hull-mounted mid-frequency
sonar source typically emits a 1-second
ping every 50 seconds representing a 2
percent duty cycle. The Navy utilizes
sonar systems and other acoustic
sensors in support of a variety of
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mission requirements. Primary uses
include the detection of and defense
against submarines (ASW) and mines
(MIW); safe navigation and effective
communications; use of unmanned
undersea vehicles; and oceanographic
surveys. Sources of sonar and other
active acoustic sources include surface
ship sonar, sonobuoys, torpedoes, and
unmanned underwater vehicles.
Ordnance and Munitions
Most ordnance and munitions used
during training events fall into three
basic categories: Projectiles (such as gun
rounds), missiles (including rockets),
and bombs. Ordnance can be further
defined by their net explosive weight
(NEW), which considers the type and
quantity of the explosive substance
without the packaging, casings, bullets,
etc. NEW is the trinitrotoluene (TNT)
equivalent of energetic material, which
is the standard measure of strength of
bombs and other explosives. For
example, a 5-inch shell fired from a
Navy gun is analyzed at approximately
9.5 pounds (lb.) (4.3 kilograms [kg]) of
NEW. The Navy also uses non-explosive
ordnance in place of explosive ordnance
in many training and testing events.
Non-explosive ordnance look and
perform similarly to explosive
ordnance, but lack the main explosive
charge.
Defense Countermeasures
Naval forces depend on effective
defensive countermeasures to protect
themselves against missile and torpedo
attack. Defensive countermeasures are
devices designed to confuse, distract,
and confound precision-guided
munitions. Defensive countermeasures
analyzed in this LOA application
include acoustic countermeasures,
which are used by surface ships and
submarines to defend against torpedo
attack. Acoustic countermeasures are
either released from ships and
submarines, or towed at a distance
behind the ship.
Classification of Non-Impulsive and
Impulsive Sources Analyzed
In order to better organize and
facilitate the analysis of approximately
300 individual sources of underwater
acoustic sound or explosive energy, a
series of source classifications, or source
bins, were developed by the Navy. The
use of source classification bins
provides the following benefits:
• Provides the ability for new sensors
or munitions to be covered under
existing regulatory authorizations, as
long as those sources fall within the
parameters of a ‘‘bin’’;
• Simplifies the source utilization
data collection and reporting
requirements anticipated under the
MMPA;
• Ensures a conservative approach to
all impact analysis, as all sources in a
single bin are modeled as the loudest
source (e.g., lowest frequency, highest
source level [the term ‘‘source level’’
refers to the loudness of a sound at its
source], longest duty cycle, or largest
net explosive weight [NEW]) within that
bin, which:
Æ Allows analysis to be conducted
more efficiently, without compromising
the results; and
Æ Provides a framework to support
the reallocation of source usage (hours/
explosives) between different source
bins, as long as the total number and
severity of marine mammal takes remain
within the overall analyzed and
authorized limits. This flexibility is
required to support evolving Navy
training requirements, which are linked
to real world events.
There are two primary types of
acoustic sources: Impulsive and nonimpulsive. A description of each source
classification is provided in Tables 1
and 2. Impulsive source class bins are
based on the NEW of the munitions or
explosive devices or the source level for
air and water guns. Non-impulsive
acoustic sources are grouped into source
class bins based on the frequency,3
source level,4 and, when warranted, the
application in which the source would
be used. The following factors further
describe the considerations associated
with the development of non-impulsive
source bins:
• Frequency of the non-impulsive
source.
Æ Low-frequency sources operate below
1 kilohertz (kHz)
Æ Mid-frequency sources operate at and
above 1 kHz, up to and including 10
kHz
Æ High-frequency sources operate above
10 kHz, up to and including 100 kHz
Æ Very high-frequency sources operate
above 100 kHz but below 200 kHz
• Source level of the non-impulsive
source.
Æ Greater than 160 decibels (dB), but
less than 180 dB
Æ Equal to 180 dB and up to 200 dB
Æ Greater than 200 dB
• Application in which the source
would be used.
Æ How a sensor is employed supports
how the sensor’s acoustic emissions are
analyzed.
Æ Factors considered include pulse
length (time source is on); beam pattern
(whether sound is emitted as a narrow,
focused beam or, as with most
explosives, in all directions); and duty
cycle (how often or how many times a
transmission occurs in a given time
period during an event).
As described in the GOA DSEIS/OEIS,
non-impulsive acoustic sources that
have low source levels (not loud),
narrow beam widths, downward
directed transmission, short pulse
lengths, frequencies beyond known
hearing ranges of marine mammals, or
some combination of these
characteristics, are not anticipated to
result in takes of protected species and
therefore were not modeled. These
sources generally meet the following
criteria and are qualitatively analyzed in
the GOA DSEIS/OEIS:
• Acoustic sources with frequencies
greater than 200 kHz (based on known
marine mammal hearing ranges)
• Sources with source levels less than
160 dB
TABLE 1—IMPULSIVE (EXPLOSIVE) TRAINING SOURCE CLASSES ANALYZED
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Source class
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.....................
.....................
.....................
.....................
.....................
5-inch projectiles ................................................................................................................................................
AGM–114 Hellfire missile ..................................................................................................................................
AGM–88 High-speed Anti-Radiation Missile .....................................................................................................
250 lb. bomb ......................................................................................................................................................
500 lb. bomb ......................................................................................................................................................
3 Bins are based on the typical center frequency
of the source. Although harmonics may be present,
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Net explosive
weight
(lbs)
Representative munitions
20:44 Feb 25, 2016
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those harmonics would be several decibels (dB)
lower than the primary frequency.
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>5–10
>10–20
>20–60
>60–100
>100–250
4 Source decibel levels are expressed in terms of
sound pressure level (SPL) and are values given in
dB referenced to 1 micropascal at 1 meter.
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TABLE 1—IMPULSIVE (EXPLOSIVE) TRAINING SOURCE CLASSES ANALYZED—Continued
Net explosive
weight
(lbs)
Source class
Representative munitions
E10 ...................
E11 ...................
E12 ...................
1,000 lb. bomb/Air-to-surface missile ................................................................................................................
MK–48 torpedo ..................................................................................................................................................
2,000 lb. bomb ...................................................................................................................................................
>250–500
>500–650
>650–1,000
TABLE 2—NON-IMPULSIVE TRAINING SOURCE CLASSES ANALYZED.
Source
class
Source class category
Mid-Frequency (MF): Tactical and non-tactical sources that
produce mid-frequency (1–10 kHz) signals.
MF1
MF3
MF4
MF5
MF6
MF11
High-Frequency (HF): Tactical and non-tactical sources that
produce high-frequency (greater than 10 kHz but less than 100
kHz) signals.
Anti-Submarine Warfare (ASW): Tactical sources such as active
sonobuoys and acoustic countermeasures systems used during
the conduct of ASW training activities.
HF1
HF6
Hull-mounted surface ship sonar (e.g., AN/SQS–53C and AN/
SQS–60).
Hull-mounted submarine sonar (e.g., AN/BQQ–10).
Helicopter-deployed dipping sonar (e.g., AN/AQS–22 and AN/
AQS–13).
Active acoustic sonobuoys (e.g., DICASS).
Active underwater sound signal devices (e.g., MK–84).
Hull-mounted surface ship sonar with an active duty cycle greater
than 80%.
Hull-mounted submarine sonar (e.g., AN/BQQ–10).
Active sources (equal to 180 dB and up to 200 dB).
ASW2
ASW3
ASW4
Torpedoes (TORP): Source classes associated with the active
acoustic signals produced by torpedoes.
Description of representative sources
TORP2
Mid-frequency Multistatic Active Coherent sonobuoy (e.g., AN/
SSQ–125).
Mid-frequency towed active acoustic countermeasure systems
(e.g., AN/SLQ–25).
Mid-frequency expendable active acoustic device countermeasures (e.g., MK–3).
Heavyweight torpedo (e.g., MK–48, electric vehicles).
Notes: dB = decibels, DICASS = Directional Command Activated Sonobuoy System, kHz = kilohertz
Training
The training activities that the Navy
proposes to conduct in the Study Area
are described in Table 3. The table is
organized according to primary mission
areas and includes the activity name,
associated stressor(s), description of the
activity, the primary platform used (e.g.,
ship or aircraft type), duration of
activity, type of non-impulsive or
impulsive sources used in the activity,
and the number of activities per year.
More detailed activity descriptions can
be found in chapter 2 of the GOA
DSEIS/OEIS. The Navy’s Proposed
Activities are anticipated to meet
training needs in the years 2016–2021.
TABLE 3—TRAINING ACTIVITIES WITHIN THE STUDY AREA
Category
Anti-Surface Warfare
(ASUW)
Impulsive ......................
Description
Gunnery Exercise, Surface-to-Surface (Ship)
(GUNEX–S–S [Ship]).
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Impulsive ......................
Sinking Exercise ................
Impulsive ......................
Bombing Exercise (Air-toSurface) (BOMBEX [A–
S]).
Anti-Submarine Warfare
(ASW)
Non-impulsive ...............
VerDate Sep<11>2014
20:44 Feb 25, 2016
Weapons/rounds/sound
source
Ship crews engage surface targets with ship’s small-,
medium-, and large-caliber guns. Some of the
small- and medium-caliber gunnery exercises analyzed include those conducted by the U.S. Coast
Guard.
Fixed-wing aircrews, surface ships and submarine firing precision-guided and non-precision weapons
against a surface target.
Fixed-wing aircrews deliver bombs against surface targets.
Small-, Medium-, and
Large-caliber high explosive rounds.
Submarine searches for, detects, and tracks submarine(s) and surface ship(s).
Mid- and high-frequency
submarine sonar.
Training activity
Tracking Exercise—Submarine (TRACKEX—
Sub).
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High explosive bombs,
missiles, Large-caliber
rounds and torpedoes.
High explosive bombs.
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TABLE 3—TRAINING ACTIVITIES WITHIN THE STUDY AREA—Continued
Category
Description
Weapons/rounds/sound
source
Maritime patrol aircraft use sonobuoys to search for,
detect, and track submarine(s).
Mid-frequency surface ship
sonar, acoustic countermeasures, and high-frequency active sources.
Mid-frequency dipping
sonar systems and
sonobuoys.
Sonobuoys, such as
DICASS sonobuoys.
Maritime patrol aircraft crews search for, detect and
track submarines using MAC sonobuoys.
mid-frequency MAC
sonobuoys.
Training activity
Non-impulsive ...............
Tracking Exercise—Surface (TRACKEX—Surface).
Surface ship searches for, tracks, and detects submarine(s).
Non-impulsive ...............
Tracking Exercise—Helicopter (TRACKEX—
Helo).
Tracking Exercise—Maritime Patrol Aircraft
(TRACKEX—MPA).
Tracking Exercise—Maritime Patrol Aircraft (MAC
Sonobuoys).
Helicopter searches, tracks, and detects submarine(s)
Non-impulsive ...............
Non-impulsive ...............
Notes: DICASS = Directional Command Activated Sonobuoy System; MAC=Multistatic Active Coherent
Summary of Impulsive and NonImpulsive Sources
and other active acoustic source class
analyzed in the Navy’s LOA request.
Table 4 provides a quantitative annual
summary of training activities by sonar
TABLE 4—ANNUAL HOURS OF SONAR AND OTHER ACTIVE ACOUSTIC SOURCES USED DURING TRAINING WITHIN THE
STUDY AREA
Source class category
Source class
Mid-Frequency (MF) Active sources from 1 to 10 kHz ............
MF1 .........................................
MF3 .........................................
MF4 .........................................
MF5 .........................................
MF6 .........................................
MF11 .......................................
High-Frequency (HF): Tactical and non-tactical sources that HF1 .........................................
produce signals greater than 10 kHz but less than 100 kHz. HF6 .........................................
Anti-Submarine Warfare (ASW) Active ASW sources ............. ASW2 ......................................
ASW3 ......................................
ASW4 ......................................
Torpedoes (TORP) Source classes associated with active TORP2 ....................................
acoustic signals produced by torpedoes.
Table 5 provides a quantitative annual
summary of training explosive source
classes analyzed in the Navy’s LOA
request.
TABLE 5—ANNUAL NUMBER OF TRAINING EXPLOSIVE SOURCE DETONATIONS
USED DURING TRAINING
WITHIN THE STUDY AREA
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Explosive class
net explosive weight
(pounds [lb.])
Annual
in-water
detonations
training
E5 (> 5–10 lb.) .....................
E6 (> 10–20 lb.) ...................
E7 (> 20–60 lb.) ...................
E8 (> 60–100 lb.) .................
E9 (> 100–250 lb.) ...............
E10 (> 250–500 lb.) .............
E11 (> 500–650 lb.) .............
E12 (> 650–1,000 lb.) ..........
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20:44 Feb 25, 2016
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2
4
6
142
32
2
4
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Duration and Location
Training activities would be
conducted in the Study Area during two
exercises of up to 21 days each per year
(for a total of up to 42 days per year) to
support a major joint training exercise
in Alaska and off the Alaskan coast that
involves the Departments of the Navy,
the Army and the Air Force, and the
U.S. Coast Guard (Coast Guard). The
Service participants report to a unified
or joint commander who coordinates the
activities planned to demonstrate and
evaluate the ability of the services to
engage in a conflict and carry out plans
in response to a threat to national
security. The exercises would occur
between the months of May and October
of each year from 2016 to 2021.
The Study Area (see Figure 1–1 of the
LOA application) is entirely at sea and
is composed of the established GOA
TMAA and a warning area in the Gulf
of Alaska. The Navy uses ‘‘at-sea’’ to
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Units
Hours
Hours
Hours
Items
Items
Hours
Hours
Hours
Hours
Hours
Items
Items
......................................
......................................
......................................
.......................................
.......................................
......................................
......................................
......................................
......................................
......................................
.......................................
.......................................
Annual use
541
48
53
25
21
78
24
80
80
546
4
5
include its training activities in the
Study Area that occur (1) on the ocean
surface, (2) beneath the ocean surface,
and (3) in the air above the ocean
surface. Navy training activities
occurring on or over the land outside
the GOA TMAA are covered under
previously prepared environmental
documentation prepared by the U.S. Air
Force and the U.S. Army.
Gulf of Alaska Temporary Maritime
Activities Area (GOA TMAA)
The GOA TMAA is a temporary area
established in conjunction with the
Federal Aviation Administration (FAA)
for up to two exercise periods of up to
21 days each, for a total of 42 days per
year, that is a surface, undersea space,
and airspace maneuver area within the
Gulf of Alaska for ships, submarines,
and aircraft to conduct required training
activities. The GOA TMAA is a polygon
roughly resembling a rectangle oriented
from northwest to southeast,
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approximately 300 nautical miles (nm)
in length by 150 nm in width, located
south of Prince William Sound and east
of Kodiak Island.
Airspace of the GOA TMAA
The airspace of the GOA TMAA
overlies the surface and subsurface
training area and is called an Altitude
Reservation (ALTRV). This ALTRV is a
temporary airspace designation,
typically requested by the Alaskan
Command (ALCOM) and coordinated
through the FAA for the duration of the
exercise. This overwater airspace
supports the majority of aircraft training
activities conducted by Navy and Joint
aircraft throughout the joint training
exercise. The ALTRV over the GOA
TMAA typically extends from the ocean
surface to 60,000 feet (ft.) (18,288 meters
[m]) above mean sea level and
encompasses 42,146 square nautical
miles (nm2) of airspace. For safety
considerations, ALTRV information is
sent via Notice to Airmen (NOTAM)/
International NOTAM so that all pilots
are aware of the area and that Air Traffic
Control will keep known Instrument
Flight Rules aircraft clear of the area.
Additionally, the GOA TMAA
overlies a majority of Warning Area W–
612 (W–612) located over Blying Sound,
towards the northwestern quadrant of
the GOA TMAA. When not included as
part of the GOA TMAA, W–612
provides 2,256 nm2 of special use
airspace for the Air Force and Coast
Guard to fulfill some of their training
requirements. Air Force, Army, National
Guard, and Coast Guard activities
conducted as part of at-sea joint training
within the GOA TMAA are included in
the DSEIS/OEIS analysis. No Navy
training activities analyzed in this
proposed rule occur in the area of W–
612 that is outside of the GOA TMAA
(see Figure 1–1 of the LOA application).
Sea and Undersea Space of the GOA
TMAA
The GOA TMAA surface and
subsurface areas are also depicted in
Figure 1–1 of the LOA application. Total
surface area of the GOA TMAA is
42,146 nm2. Due to weather conditions,
annual joint training activities are
typically conducted during the summer
months (April–October). The GOA
TMAA undersea area lies beneath the
surface area as depicted in Figure 1–1 of
the LOA application. The undersea area
extends to the seafloor.
The complex bathymetric and
oceanographic conditions, including a
continental shelf, submarine canyons,
numerous seamounts, and fresh water
infusions from multiple sources, create
a challenging environment in which to
search for and detect submarines in
ASW training activities. In the summer,
the GOA TMAA provides a safe coldwater training environment that
resembles other areas where Navy may
need to operate in a real-world scenario.
The GOA TMAA meets large-scale
joint exercise training objectives to
support naval and joint operational
readiness by providing a
‘‘geographically realistic’’ training area
for U.S. Pacific Command, Joint Task
Force Commander scenario-based
training, and supports the mission
requirement of Alaskan Command
(ALCOM) to conduct joint training for
Alaska-based forces. The strategic vision
of the Commander, U.S. Pacific Fleet is
that the training area support naval
operational readiness by providing a
realistic, live-training environment for
forces assigned to the Pacific Fleet and
other users with the capability and
capacity to support current, emerging,
and future training requirements.
Description of Marine Mammals in the
Area of the Specified Activities
Marine mammal species known to
occur in the Study Area and their
currently recognized stocks are
presented in Table 6 consistent with the
NMFS’ U.S. Pacific Marine Mammal
Stock Assessment Report (Carretta et al.,
2015) and the Alaska Marine Mammal
Stock Assessment Report (Muto and
Angliss, 2015). Twenty-two marine
mammal species have confirmed or
possible occurrence within or adjacent
to the Study Area, including seven
species of baleen whales (mysticetes),
eight species of toothed whales
(odontocetes), six species of seals
(pinnipeds), and the sea otter
(mustelid). Nine of these species are
listed under the ESA: Blue whale, fin
whale, humpback whale, sei whale,
sperm whale, gray whale (Western
North Pacific stock), North Pacific right
whale, Steller sea lion (Western U.S.
stock), and sea otter. All these species
are managed by NMFS or the U.S. Fish
and Wildlife Service (USFWS) in the
U.S. Exclusive Economic Zone (EEZ).
The species carried forward for
analysis are those likely to be found in
the Study Area based on the most recent
data available, and do not include
stocks or species that may have once
inhabited or transited the area but have
not been sighted in recent years (e.g.,
species which were extirpated because
of factors such as nineteenth and
twentieth century commercial
exploitation). Several species that may
be present in the Gulf of Alaska have an
extremely low probability of presence in
the Study Area. These species are
considered extralimital, meaning there
may be a small number of sighting or
stranding records within the Study
Area, but the area of concern is outside
the species’ range of normal occurrence.
These species include beluga whale
(Delphinapterus leucas), false killer
whale (Pseudorca crassidens), shortfinned pilot whale (Globicephala
macrorhynchus), northern right whale
dolphin (Lissodelphis borealis), and
Risso’s dolphin (Grampus griseus), and
have been excluded from subsequent
analysis.
TABLE 6—MARINE MAMMALS WITH POSSIBLE OR CONFIRMED PRESENCE WITHIN THE STUDY AREA
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
Common name
Scientific name 1
Stock abundance 3
(CV)
Stock 2
Occurrence in
region 4
ESA/MMPA Status
Order Cetacea
Suborder Mysticeti (baleen whales)
Family Balaenidae (right whales)
North Pacific right
whale.
Eubalaena japonica ..
Eastern North Pacific
31 (0.23) ...................
Rare ..........................
Endangered/Depleted.
Endangered/D Depleted.
Endangered/D Depleted.
Family Balaenopteridae (rorquals)
Humpback whale ........
20:44 Feb 25, 2016
Jkt 238001
Central North Pacific
10,252 (0.042) ..........
Likely .........................
Western North Pacific
VerDate Sep<11>2014
Megaptera
novaeangliae.
893 (0.079) ...............
Likely .........................
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9957
TABLE 6—MARINE MAMMALS WITH POSSIBLE OR CONFIRMED PRESENCE WITHIN THE STUDY AREA—Continued
Blue whale ..................
Fin whale ....................
Sei whale ....................
Minke whale ...............
Stock 2
Stock abundance 3
(CV)
Occurrence in
region 4
Eastern North Pacific
1,647 (0.07) ..............
Central North Pacific
Common name
81 (1.14) ...................
Balaenoptera
physalus.
Balaenoptera borealis
Northeast Pacific .......
Eastern North Pacific
1,368 (minimum estimate) (n/a).
126 (0.53) .................
Seasonal; highest
likelihood July to
December.
Seasonal; highest
likelihood July to
December.
Likely .........................
Balaenoptera
acutorostrata.
Alaska .......................
Not available .............
Scientific name 1
Balaenoptera
musculus.
Rare ..........................
ESA/MMPA Status
Endangered/D Depleted.
Endangered/D Depleted.
Endangered/D Depleted.
Endangered/D Depleted.
Likely.
Family Eschrichtiidae (gray whale)
Gray whale .................
Eschrichtius robustus
Eastern North Pacific
20,990 (0.05) ............
Western North Pacific
140 (0.043) ...............
Likely: Highest numbers during seasonal migrations.
Rare: Individuals migrate through GOA.
Endangered/D Depleted.
Suborder Odontoceti (toothed whales)
Family Physeteridae (sperm whale)
Sperm whale ..............
Physeter
macrocephalus.
North Pacific .............
Not available .............
Likely; More likely in
waters > 1,000 m
depth, most often >
2,000 m.
Family Delphinidae (dolphins)
Killer whale .................
Orcinus orca .............
Alaska Resident ........
Eastern North Pacific
Offshore.
AT1 Transient ...........
Pacific white-sided dolphin.
GOA, Aleutian Island,
and Bering Sea
Transient.
North Pacific .............
Lagenorhynchus
obliquidens.
2,347 (n/a) ................
211: includes known
offshore killer
whales along the
U.S. west coast,
Canada, and Alaska (n/a).
7 ................................
587 ............................
26,880; specific to the
GOA, not the management stock (n/
a).
Likely.
Infrequent: few
sightings.
Rare; more likely inside Prince William
Sound and Kenai
Fjords.
Likely.
Likely.
Family Phocoenidae (porpoises)
Harbor porpoise .........
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Phocoenoides dalli ....
GOA ..........................
31,046 (0.21) ............
Southeast Alaska ......
Dall’s porpoise ............
Phocoena phocoena
11,146 (0.24) ............
Alaska .......................
83,400 (0.097); based
on survey data
from 1987–1991.
Likely in nearshore
locations.
Likely in nearshore
locations.
Likely.
Family Ziphiidae (beaked whales)
Cuvier’s beaked whale
Baird’s beaked whale
Stejneger’s beaked
whale.
VerDate Sep<11>2014
Ziphius cavirostris .....
Berardius bairdii ........
Mesoplodon
stejnegeri.
20:44 Feb 25, 2016
Jkt 238001
Alaska .......................
Alaska .......................
Alaska .......................
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Not available .............
Not available .............
Not available .............
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Likely.
Likely.
Likely.
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Endangered/D Depleted.
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TABLE 6—MARINE MAMMALS WITH POSSIBLE OR CONFIRMED PRESENCE WITHIN THE STUDY AREA—Continued
Common name
Scientific name 1
Stock abundance 3
(CV)
Stock 2
Occurrence in
region 4
ESA/MMPA Status
Order Carnivora
Suborder Pinnipedia 5
Family Otariidae (fur seals and sea lions)
Steller sea lion ...........
Eumetopias jubatus ..
Eastern U.S. .............
U.S. ...........................
59,968 (minimum estimate) (n/a).
49,497 (minimum estimate) (n/a).
296,750 (n/a) ............
Rare.
Eastern Pacific ..........
648,534 (n/a) ............
Likely .........................
Western U.S. ............
California sea lion ......
Northern fur seal ........
Zalophus
californianus.
Callorhinus ursinus ...
Likely.
Likely .........................
Endangered/D Depleted.
Depleted.
Family Phocidae (true seals)
Northern elephant seal
Likely.
Aleutian Islands ........
Pribilof Islands ..........
Bristol Bay .................
N. Kodiak ..................
6,431 (n/a) ................
232 (n/a) ...................
32,350 (n/a) ..............
8,321 (n/a) ................
19,199 (n/a) ..............
29,889 (n/a) ..............
Cook Inlet/Shelikof ....
Glacier Bay/Icy Strait
27,386 (n/a) ..............
7,210 (n/a) ................
Lynn Canal/S Stephens.
Sitka/Chatham ..........
9,478 (n/a) ................
Extralimital
Extralimital.
Extralimital.
Rare (inshore
waters).
Rare (inshore
waters).
Rare (inshore
waters).
Extralimital.
Rare (inshore
waters).
Extralimital.
14,855 (n/a) ..............
Dixon/Cape Decision
Histriophoca fasciata
179,000 (n/a) ............
Prince William Sound
Ribbon seal ................
California Breeding ...
S. Kodiak ..................
Harbor seal .................
Mirounga
angustirostris.
Phoca vitulina ...........
18,105 (n/a) ..............
Clarence Strait ..........
Alaska .......................
31,634 (n/a) ..............
184,000 .....................
Rare (inshore
waters).
Rare (inshore
waters).
Extralimital.
Rare.
Family Mustelidae (otters) 6
Northern sea otter ......
Enhydra lutris
kenyoni.
Southeast Alaska ......
10,563 .......................
Rare.
Southcentral Alaska ..
Southwest Alaska .....
15,090 .......................
47,676 .......................
Rare.
Rare ..........................
Threatened.
1 Taxonomy
follows Perrin et al. (2009).
names and abundance estimates from Muto and Angliss (2015) and Carretta et al. (2015) except where noted.
stated coefficient of variation (CV) from the NMFS Stock Assessement Reports is an indicator of uncertainty in the abundance estimate
and describes the amount of variation with respect to the population mean. It is expressed as a fraction or sometimes a percentage and can
range upward from zero, indicating no uncertainty, to high values. For example, a CV of 0.85 would indicate high uncertainty in the population
estimate. When the CV exceeds 1.0, the estimate is very uncertain. The uncertainty associated with movements of animals into or out of an area
(due to factors such as availability of prey or changing oceanographic conditions) is much larger than is indicated by the CVs that are given.
4 EXTRALIMITAL: There may be a small number of sighting or stranding records, but the area is outside the species range of normal occurrence. RARE: The distribution of the species is near enough to the area that the species could occur there, or there are a few confirmed
sightings. INFREQUENT: Confirmed, but irregular sightings or acoustic detections. LIKELY: Confirmed and regular sightings or acoustic detections of the species in the area year-round. SEASONAL: Confirmed and regular sightings or acoustic detections of the species in the area on a
seasonal basis.
5 There are no data regarding the CV for some of the pinniped species given that abundance is determined by different methods than those
used for cetaceans.
6 There are no data regarding the CV for sea otter given that abundance is determined by different methods than those used for cetaceans.
Notes: CV = coefficient of variation, ESA = Endangered Species Act, GOA = Gulf of Alaska, m = meter(s), MMPA = Marine Mammal Protection Act, n/a = not available, U.S. = United States.
2 Stock
mstockstill on DSK4VPTVN1PROD with PROPOSALS2
3 The
Information on the status,
distribution, abundance, and
vocalizations of marine mammal species
in the Study Area may be viewed in
Chapter 4 of the LOA application
(https://www.nmfs.noaa.gov/pr/permits/
incidental/military.htm). Additional
information on the general biology and
ecology of marine mammals are
VerDate Sep<11>2014
20:44 Feb 25, 2016
Jkt 238001
included in the GOA DSEIS/OEIS. In
addition, NMFS annually publishes
Stock Assessment Reports (SARs) for all
marine mammals in U.S. EEZ waters,
including stocks that occur within the
Study Area (U.S. Pacific Marine
Mammal Stock Assessments, Carretta et
al., 2015; Alaska Marine Mammal Stock
Assessments, Muto and Angliss, 2015).
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Marine Mammal Hearing and
Vocalizations
Cetaceans have an auditory anatomy
that follows the basic mammalian
pattern, with some changes to adapt to
the demands of hearing underwater. The
typical mammalian ear is divided into
an outer ear, middle ear, and inner ear.
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The outer ear is separated from the
inner ear by a tympanic membrane, or
eardrum. In terrestrial mammals, the
outer ear, eardrum, and middle ear
transmit airborne sound to the inner ear,
where the sound waves are propagated
through the cochlear fluid. Since the
impedance of water is close to that of
the tissues of a cetacean, the outer ear
is not required to transduce sound
energy as it does when sound waves
travel from air to fluid (inner ear).
Sound waves traveling through the
inner ear cause the basilar membrane to
vibrate. Specialized cells, called hair
cells, respond to the vibration and
produce nerve pulses that are
transmitted to the central nervous
system. Acoustic energy causes the
basilar membrane in the cochlea to
vibrate. Sensory cells at different
positions along the basilar membrane
are excited by different frequencies of
sound (Pickles, 1998).
Marine mammal vocalizations often
extend both above and below the range
of human hearing; vocalizations with
frequencies lower than 20 Hz are
labeled as infrasonic and those higher
than 20 kHz as ultrasonic (National
Research Council (NRC), 2003; Figure
4–1). Measured data on the hearing
abilities of cetaceans are sparse,
particularly for the larger cetaceans such
as the baleen whales. The auditory
thresholds of some of the smaller
odontocetes have been determined in
captivity. It is generally believed that
cetaceans should at least be sensitive to
the frequencies of their own
vocalizations. Comparisons of the
anatomy of cetacean inner ears and
models of the structural properties and
the response to vibrations of the ear’s
components in different species provide
an indication of likely sensitivity to
various sound frequencies. The ears of
small toothed whales are optimized for
receiving high-frequency sound, while
baleen whale inner ears are best in low
to infrasonic frequencies (Ketten, 1992;
1997; 1998).
Baleen whale vocalizations are
composed primarily of frequencies
below 1 kHz, and some contain
fundamental frequencies as low as 16
Hz (Watkins et al., 1987; Richardson et
al., 1995; Rivers, 1997; Moore et al.,
1998; Stafford et al., 1999; Wartzok and
Ketten, 1999) but can be as high as 24
kHz (humpback whale; Au et al., 2006).
Clark and Ellison (2004) suggested that
baleen whales use low-frequency
sounds not only for long-range
communication, but also as a simple
form of echo ranging, using echoes to
navigate and orient relative to physical
features of the ocean. Information on
auditory function in baleen whales is
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extremely lacking. Sensitivity to lowfrequency sound by baleen whales has
been inferred from observed
vocalization frequencies, observed
reactions to playback of sounds, and
anatomical analyses of the auditory
system. Although there is apparently
much variation, the source levels of
most baleen whale vocalizations lie in
the range of 150–190 dB re 1
microPascal (mPa) at 1 m. Lowfrequency vocalizations made by baleen
whales and their corresponding
auditory anatomy suggest that they have
good low-frequency hearing (Ketten,
2000), although specific data on
sensitivity, frequency or intensity
discrimination, or localization abilities
are lacking. Marine mammals, like all
mammals, have typical U-shaped
audiograms that begin with relatively
low sensitivity (high threshold) at some
specified low frequency with increased
sensitivity (low threshold) to a species
specific optimum followed by a
generally steep rise at higher
frequencies (high threshold) (Fay, 1988).
The toothed whales produce a wide
variety of sounds, which include
species-specific broadband ‘‘clicks’’
with peak energy between 10 and 200
kHz, individually variable ‘‘burst pulse’’
click trains, and constant frequency or
frequency-modulated (FM) whistles
ranging from 4 to 16 kHz (Wartzok and
Ketten, 1999). The general consensus is
that the tonal vocalizations (whistles)
produced by toothed whales play an
important role in maintaining contact
between dispersed individuals, while
broadband clicks are used during
echolocation (Wartzok and Ketten,
1999). Burst pulses have also been
strongly implicated in communication,
with some scientists suggesting that
they play an important role in agonistic
encounters (McCowan and Reiss, 1995),
while others have proposed that they
represent ‘‘emotive’’ signals in a broader
sense, possibly representing graded
communication signals (Herzing, 1996).
Sperm whales, however, are known to
produce only clicks, which are used for
both communication and echolocation
(Whitehead, 2003). Most of the energy of
toothed whale social vocalizations is
concentrated near 10 kHz, with source
levels for whistles as high as 100 to 180
dB re 1 mPa at 1 m (Richardson et al.,
1995). No odontocete has been shown
audiometrically to have acute hearing
(<80 dB re 1 mPa) below 500 Hz (DoN,
2001). Sperm whales produce clicks,
which may be used to echolocate
(Mullins et al., 1988), with a frequency
range from less than 100 Hz to 30 kHz
and source levels up to 230 dB re 1 mPa
1 m or greater (Mohl et al., 2000).
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Brief Background on Sound
An understanding of the basic
properties of underwater sound is
necessary to comprehend many of the
concepts and analyses presented in this
proposed rule. A summary is included
below.
Sound is a wave of pressure variations
propagating through a medium (e.g.,
water). Pressure variations are created
by compressing and relaxing the
medium. Sound measurements can be
expressed in two forms: Intensity and
pressure. Acoustic intensity is the
average rate of energy transmitted
through a unit area in a specified
direction and is expressed in watts per
square meter (W/m2). Acoustic intensity
is rarely measured directly, but rather
from ratios of pressures; the standard
reference pressure for underwater sound
is 1 mPa; for airborne sound, the
standard reference pressure is 20 mPa
(Richardson et al., 1995).
Acousticians have adopted a
logarithmic scale for sound intensities,
which is denoted in decibels (dB).
Decibel measurements represent the
ratio between a measured pressure value
and a reference pressure value (in this
case 1 mPa or, for airborne sound, 20
mPa). The logarithmic nature of the scale
means that each 10-dB increase is a tenfold increase in acoustic power (and a
20-dB increase is then a 100-fold
increase in power; and a 30-dB increase
is a 1,000-fold increase in power). A tenfold increase in acoustic power does not
mean that the sound is perceived as
being ten times louder, however.
Humans perceive a 10-dB increase in
sound level as a doubling of loudness,
and a 10-dB decrease in sound level as
a halving of loudness. The term ‘‘sound
pressure level’’ implies a decibel
measure and a reference pressure that is
used as the denominator of the ratio.
Throughout this proposed rule, NMFS
uses 1 mPa (denoted re: 1mPa) as a
standard reference pressure unless
noted otherwise.
It is important to note that decibel
values underwater and decibel values in
air are not the same (different reference
pressures and densities/sound speeds
between media) and should not be
directly compared. Because of the
different densities of air and water and
the different decibel standards (i.e.,
reference pressures) in air and water, a
sound with the same level in air and in
water would be approximately 62 dB
lower in air. Thus, a sound that
measures 160 dB (re 1 mPa) underwater
would have the same approximate
effective level as a sound that is 98 dB
(re 20 mPa) in air.
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Sound frequency is measured in
cycles per second, or Hertz (abbreviated
Hz), and is analogous to musical pitch;
high-pitched sounds contain high
frequencies and low-pitched sounds
contain low frequencies. Natural sounds
in the ocean span a huge range of
frequencies: From earthquake noise at 5
Hz to harbor porpoise clicks at 150,000
Hz (150 kHz). These sounds are so low
or so high in pitch that humans cannot
even hear them; acousticians call these
infrasonic (typically below 20 Hz) and
ultrasonic (typically above 20,000 Hz)
sounds, respectively. A single sound
may be made up of many different
frequencies together. Sounds made up
of only a small range of frequencies are
called ‘‘narrowband’’, and sounds with
a broad range of frequencies are called
‘‘broadband’’; explosives are an example
of a broadband sound source and active
tactical sonars are an example of a
narrowband sound source.
When considering the influence of
various kinds of sound on the marine
environment, it is necessary to
understand that different kinds of
marine life are sensitive to different
frequencies of sound. Current data
indicate that not all marine mammal
species have equal hearing capabilities
(Richardson et al., 1995; Southall et al.,
1997; Wartzok and Ketten, 1999; Au and
Hastings, 2008).
Southall et al. (2007) designated
‘‘functional hearing groups’’ for marine
mammals based on available behavioral
data; audiograms derived from auditory
evoked potentials; anatomical modeling;
and other data. Southall et al. (2007)
also estimated the lower and upper
frequencies of functional hearing for
each group. However, animals are less
sensitive to sounds at the outer edges of
their functional hearing range and are
more sensitive to a range of frequencies
within the middle of their functional
hearing range. Note that direct
measurements of hearing sensitivity do
not exist for all species of marine
mammals, including low-frequency
cetaceans. The functional hearing
groups and the associated frequencies
developed by Southall et al. (2007) were
revised by Finneran and Jenkins (2012)
and have been further modified by
NOAA. Table 7 provides a summary of
sound production and general hearing
capabilities for marine mammal species
(note that values in this table are not
meant to reflect absolute possible
maximum ranges, rather they represent
the best known ranges of each
functional hearing group). For purposes
of the analysis in this proposed rule,
marine mammals are arranged into the
following functional hearing groups
based on their generalized hearing
sensitivities: High-frequency cetaceans,
mid-frequency cetaceans, low-frequency
cetaceans (mysticetes), phocids (true
seals), otariids (sea lion and fur seals),
and mustelids (sea otters). A detailed
discussion of the functional hearing
groups can be found in Southall et al.
(2007) and Finneran and Jenkins (2012).
TABLE 7—MARINE MAMMAL FUNCTIONAL HEARING GROUPS
Functional hearing
range *
Functional hearing group
Low-frequency (LF) cetaceans (baleen whales) .....................................................................................................................
Mid-frequency (MF) cetaceans (dolphins, toothed whales, beaked whales, bottlenose whales) ...........................................
High-frequency (HF) cetaceans (true porpoises, Kogia, river dolphins, cephalorhynchid, Lagenorhynchus cruciger & L.
australis).
Phocid pinnipeds (underwater) (true seals) ............................................................................................................................
Otariid pinnipeds (underwater) (sea lions and fur seals) ........................................................................................................
7 Hz to 25 kHz.
150 Hz to 160 kHz.
200 Hz to 180 kHz.
75 Hz to 100 kHz.
100 Hz to 48 kHz.
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Adapted and derived from Southall et al. (2007)
* Represents frequency band of hearing for entire group as a composite (i.e., all species within the group), where individual species’ hearing
ranges are typically not as broad. Functional hearing is defined as the range of frequencies a group hears without incorporating non-acoustic
mechanisms (Wartzok and Ketten, 1999). This is ∼60 to ∼70 dB above best hearing sensitivity (Southall et al., 2007) for all functional hearing
groups except LF cetaceans, where no direct measurements on hearing are available. For LF cetaceans, the lower range is based on recommendations from Southall et al., 2007 and the upper range is based on information on inner ear anatomy and vocalizations.
When sound travels (propagates) from
its source, its loudness decreases as the
distance traveled by the sound
increases. Thus, the loudness of a sound
at its source is higher than the loudness
of that same sound a kilometer away.
Acousticians often refer to the loudness
of a sound at its source (typically
referenced to one meter from the source)
as the source level and the loudness of
sound elsewhere as the received level
(i.e., typically the receiver). For
example, a humpback whale 3 km from
a device that has a source level of 230
dB may only be exposed to sound that
is 160 dB loud, depending on how the
sound travels through water (e.g.,
spherical spreading [3 dB reduction
with doubling of distance] was used in
this example). As a result, it is
important to understand the difference
between source levels and received
levels when discussing the loudness of
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sound in the ocean or its impacts on the
marine environment.
As sound travels from a source, its
propagation in water is influenced by
various physical characteristics,
including water temperature, depth,
salinity, and surface and bottom
properties that cause refraction,
reflection, absorption, and scattering of
sound waves. Oceans are not
homogeneous and the contribution of
each of these individual factors is
extremely complex and interrelated.
The physical characteristics that
determine the sound’s speed through
the water will change with depth,
season, geographic location, and with
time of day (as a result, in actual active
sonar operations, crews will measure
oceanic conditions, such as sea water
temperature and depth, to calibrate
models that determine the path the
sonar signal will take as it travels
through the ocean and how strong the
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sound signal will be at a given range
along a particular transmission path). As
sound travels through the ocean, the
intensity associated with the wavefront
diminishes, or attenuates. This decrease
in intensity is referred to as propagation
loss, also commonly called transmission
loss.
Metrics Used in This Proposed Rule
This section includes a brief
explanation of the two sound
measurements (sound pressure level
(SPL) and sound exposure level (SEL))
frequently used to describe sound levels
in the discussions of acoustic effects in
this proposed rule.
Sound pressure level (SPL)—Sound
pressure is the sound force per unit
area, and is usually measured in
micropascals (mPa), where 1 Pa is the
pressure resulting from a force of one
newton exerted over an area of one
square meter. SPL is expressed as the
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ratio of a measured sound pressure and
a reference level.
SPL (in dB) = 20 log (pressure/reference
pressure)
The commonly used reference
pressure level in underwater acoustics
is 1 mPa, and the units for SPLs are dB
re: 1 mPa. SPL is an instantaneous
pressure measurement and can be
expressed as the peak, the peak-peak, or
the root mean square (rms). Root mean
square pressure, which is the square
root of the arithmetic average of the
squared instantaneous pressure values,
is typically used in discussions of the
effects of sounds on vertebrates and all
references to SPL in this proposed rule
refer to the root mean square. SPL does
not take the duration of exposure into
account. SPL is the applicable metric
used in the risk continuum, which is
used to estimate behavioral harassment
takes (see Level B Harassment Risk
Function (Behavioral Harassment)
Section).
Sound exposure level (SEL)—SEL is
an energy metric that integrates the
squared instantaneous sound pressure
over a stated time interval. The units for
SEL are dB re: 1 mPa2-s. Below is a
simplified formula for SEL.
SEL = SPL + 10log (duration in seconds)
As applied to active sonar, the SEL
includes both the SPL of a sonar ping
and the total duration. Longer duration
pings and/or pings with higher SPLs
will have a higher SEL. If an animal is
exposed to multiple pings, the SEL in
each individual ping is summed to
calculate the cumulative SEL. The
cumulative SEL depends on the SPL,
duration, and number of pings received.
The thresholds that NMFS uses to
indicate at what received level the onset
of temporary threshold shift (TTS) and
permanent threshold shift (PTS) in
hearing are likely to occur are expressed
as cumulative SEL.
other components of their proposed
activities. In this proposed rule, NMFS
analyzes the potential effects on marine
mammals from exposure to nonimpulsive sound sources (sonar and
other active acoustic sources) and
impulsive sound sources (underwater
detonations).
For the purpose of MMPA
authorizations, NMFS’ effects
assessments serve four primary
purposes: (1) To prescribe the
permissible methods of taking (i.e.,
Level B harassment (behavioral
harassment), Level A harassment
(injury), or mortality, including an
identification of the number and types
of take that could occur by harassment
or mortality) and to prescribe other
means of effecting the least practicable
adverse impact on such species or stock
and its habitat (i.e., mitigation); (2) to
determine whether the specified activity
would have a negligible impact on the
affected species or stocks of marine
mammals (based on the likelihood that
the activity would adversely affect the
species or stock through effects on
annual rates of recruitment or survival);
(3) to determine whether the specified
activity would have an unmitigable
adverse impact on the availability of the
species or stock(s) for subsistence uses;
and (4) to prescribe requirements
pertaining to monitoring and reporting.
This section focuses qualitatively on
the different ways that non-impulsive
and impulsive sources may affect
marine mammals (some of which NMFS
would not classify as harassment). Then
the Estimated Take of Marine Mammals
section discusses how the potential
effects of non-impulsive and impulsive
sources on marine mammals will be
related to the MMPA definitions of
Level A and Level B Harassment, and
attempts to quantify those effects.
Potential Effects of Specified Activities
on Marine Mammals
The Navy has requested authorization
for the take of marine mammals that
may occur incidental to training
activities in the Study Area. The Navy
has analyzed potential impacts to
marine mammals from impulsive and
non-impulsive sound sources.
Other potential impacts to marine
mammals from training activities in the
Study Area were analyzed in the GOA
DSEIS/OEIS, in consultation with
NMFS as a cooperating agency, and
determined to be unlikely to result in
marine mammal harassment. Therefore,
the Navy has not requested
authorization for take of marine
mammals that might occur incidental to
Direct Physiological Effects
Based on the literature, there are two
basic ways that non-impulsive sources
might directly result in physical trauma
or damage: Noise-induced loss of
hearing sensitivity (more commonlycalled ‘‘threshold shift’’) and
acoustically mediated bubble growth.
Separately, an animal’s behavioral
reaction to an acoustic exposure might
lead to physiological effects that might
ultimately lead to injury or death, which
is discussed later in the Stranding
section.
Threshold Shift (noise-induced loss of
hearing)—When animals exhibit
reduced hearing sensitivity (i.e., sounds
must be louder for an animal to detect
them) following exposure to an intense
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9961
sound or sound for long duration, it is
referred to as a noise-induced threshold
shift (TS). An animal can experience
temporary threshold shift (TTS) or
permanent threshold shift (PTS). TTS
can last from minutes or hours to days
(i.e., there is complete recovery), can
occur in specific frequency ranges (i.e.,
an animal might only have a temporary
loss of hearing sensitivity between the
frequencies of 1 and 10 kHz), and can
be of varying amounts (for example, an
animal’s hearing sensitivity might be
reduced initially by only 6 dB or
reduced by 30 dB). PTS is permanent,
but some recovery is possible. PTS can
also occur in a specific frequency range
and amount, as mentioned above for
TTS.
The following physiological
mechanisms are thought to play a role
in inducing auditory TS: Effects to
sensory hair cells in the inner ear that
reduce their sensitivity, modification of
the chemical environment within the
sensory cells, residual muscular activity
in the middle ear, displacement of
certain inner ear membranes, increased
blood flow, and post-stimulatory
reduction in both efferent and sensory
neural output (Southall et al., 2007).
The amplitude, duration, frequency,
temporal pattern, and energy
distribution of sound exposure all can
affect the amount of associated TS and
the frequency range in which it occurs.
As amplitude and duration of sound
exposure increase, so, generally, does
the amount of TS, along with the
recovery time. For intermittent sounds,
less TS could occur than compared to a
continuous exposure with the same
energy (some recovery could occur
between intermittent exposures
depending on the duty cycle between
sounds) (Kryter et al., 1966; Ward,
1997). For example, one short but loud
(higher SPL) sound exposure may
induce the same impairment as one
longer but softer sound, which in turn
may cause more impairment than a
series of several intermittent softer
sounds with the same total energy
(Ward, 1997). Additionally, though TTS
is temporary, prolonged exposure to
sounds strong enough to elicit TTS, or
shorter-term exposure to sound levels
well above the TTS threshold, can cause
PTS, at least in terrestrial mammals
(Kryter, 1985). Although in the case of
mid- and high-frequency active sonar
(MFAS/HFAS), animals are not
expected to be exposed to levels high
enough or durations long enough to
result in PTS.
PTS is considered auditory injury
(Southall et al., 2007). Irreparable
damage to the inner or outer cochlear
hair cells may cause PTS; however,
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other mechanisms are also involved,
such as exceeding the elastic limits of
certain tissues and membranes in the
middle and inner ears and resultant
changes in the chemical composition of
the inner ear fluids (Southall et al.,
2007).
Although the published body of
scientific literature contains numerous
theoretical studies and discussion
papers on hearing impairments that can
occur with exposure to a loud sound,
only a few studies provide empirical
information on the levels at which
noise-induced loss in hearing sensitivity
occurs in nonhuman animals. For
marine mammals, published data are
limited to the captive bottlenose
dolphin, beluga, harbor porpoise, and
Yangtze finless porpoise (Finneran et
al., 2000, 2002b, 2003, 2005a, 2007,
2010a, 2010b; Finneran and Schlundt,
2010; Lucke et al., 2009; Mooney et al.,
2009a, 2009b; Popov et al., 2011a,
2011b; Kastelein et al., 2012a; Schlundt
et al., 2000; Nachtigall et al., 2003,
2004). For pinnipeds in water, data are
limited to measurements of TTS in
harbor seals, an elephant seal, and
California sea lions (Kastak et al., 1999,
2005; Kastelein et al., 2012b).
Marine mammal hearing plays a
critical role in communication with
conspecifics, and interpretation of
environmental cues for purposes such
as predator avoidance and prey capture.
Depending on the degree (elevation of
threshold in dB), duration (i.e., recovery
time), and frequency range of TTS, and
the context in which it is experienced,
TTS can have effects on marine
mammals ranging from discountable to
serious (similar to those discussed in
auditory masking, below). For example,
a marine mammal may be able to readily
compensate for a brief, relatively small
amount of TTS in a non-critical
frequency range that occurs during a
time where ambient noise is lower and
there are not as many competing sounds
present. Alternatively, a larger amount
and longer duration of TTS sustained
during time when communication is
critical for successful mother/calf
interactions could have more serious
impacts. Also, depending on the degree
and frequency range, the effects of PTS
on an animal could range in severity,
although it is considered generally more
serious because it is a permanent
condition. Of note, reduced hearing
sensitivity as a simple function of aging
has been observed in marine mammals,
as well as humans and other taxa
(Southall et al., 2007), so one can infer
that strategies exist for coping with this
condition to some degree, though likely
not without cost.
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Acoustically Mediated Bubble
Growth—One theoretical cause of injury
to marine mammals is rectified
diffusion (Crum and Mao, 1996), the
process of increasing the size of a
bubble by exposing it to a sound field.
This process could be facilitated if the
environment in which the ensonified
bubbles exist is supersaturated with gas.
Repetitive diving by marine mammals
can cause the blood and some tissues to
accumulate gas to a greater degree than
is supported by the surrounding
environmental pressure (Ridgway and
Howard, 1979). The deeper and longer
dives of some marine mammals (for
example, beaked whales) are
theoretically predicted to induce greater
supersaturation (Houser et al., 2001b). If
rectified diffusion were possible in
marine mammals exposed to high-level
sound, conditions of tissue
supersaturation could theoretically
speed the rate and increase the size of
bubble growth. Subsequent effects due
to tissue trauma and emboli would
presumably mirror those observed in
humans suffering from decompression
sickness.
It is unlikely that the short duration
of sonar pings would be long enough to
drive bubble growth to any substantial
size, if such a phenomenon occurs.
However, an alternative but related
hypothesis has also been suggested:
Stable bubbles could be destabilized by
high-level sound exposures such that
bubble growth then occurs through
static diffusion of gas out of the tissues.
In such a scenario the marine mammal
would need to be in a gassupersaturated state for a long enough
period of time for bubbles to become of
a problematic size. Recent research with
ex vivo supersaturated bovine tissues
suggested that, for a 37 kHz signal, a
sound exposure of approximately 215
dB referenced to (re) 1 mPa would be
required before microbubbles became
destabilized and grew (Crum et al.,
2005). Assuming spherical spreading
loss and a nominal sonar source level of
235 dB re 1 mPa at 1 m, a whale would
need to be within 10 m (33 ft.) of the
sonar dome to be exposed to such sound
levels. Furthermore, tissues in the study
were supersaturated by exposing them
to pressures of 400–700 kilopascals for
periods of hours and then releasing
them to ambient pressures. Assuming
the equilibration of gases with the
tissues occurred when the tissues were
exposed to the high pressures, levels of
supersaturation in the tissues could
have been as high as 400–700 percent.
These levels of tissue supersaturation
are substantially higher than model
predictions for marine mammals
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(Houser et al., 2001; Saunders et al.,
2008). It is improbable that this
mechanism is responsible for stranding
events or traumas associated with
beaked whale strandings. Both the
degree of supersaturation and exposure
levels observed to cause microbubble
destabilization are unlikely to occur,
either alone or in concert.
Yet another hypothesis
(decompression sickness) has
speculated that rapid ascent to the
surface following exposure to a startling
sound might produce tissue gas
saturation sufficient for the evolution of
nitrogen bubbles (Jepson et al., 2003;
´
Fernandez et al., 2005; Fernandez et al.,
2012). In this scenario, the rate of ascent
would need to be sufficiently rapid to
compromise behavioral or physiological
protections against nitrogen bubble
formation. Alternatively, Tyack et al.
(2006) studied the deep diving behavior
of beaked whales and concluded that:
‘‘Using current models of breath-hold
diving, we infer that their natural diving
behavior is inconsistent with known
problems of acute nitrogen
supersaturation and embolism.’’
Collectively, these hypotheses can be
referred to as ‘‘hypotheses of
acoustically mediated bubble growth.’’
Although theoretical predictions
suggest the possibility for acoustically
mediated bubble growth, there is
considerable disagreement among
scientists as to its likelihood (Piantadosi
and Thalmann, 2004; Evans and Miller,
2003). Crum and Mao (1996)
hypothesized that received levels would
have to exceed 190 dB in order for there
to be the possibility of significant
bubble growth due to supersaturation of
gases in the blood (i.e., rectified
diffusion). More recent work conducted
by Crum et al. (2005) demonstrated the
possibility of rectified diffusion for
short duration signals, but at SELs and
tissue saturation levels that are highly
improbable to occur in diving marine
mammals. To date, energy levels (ELs)
predicted to cause in vivo bubble
formation within diving cetaceans have
not been evaluated (NOAA, 2002b).
Although it has been argued that
traumas from some recent beaked whale
strandings are consistent with gas
emboli and bubble-induced tissue
separations (Jepson et al., 2003), there is
no conclusive evidence of this.
However, Jepson et al. (2003, 2005) and
Fernandez et al. (2004, 2005, 2012)
concluded that in vivo bubble
formation, which may be exacerbated by
deep, long-duration, repetitive dives
may explain why beaked whales appear
to be particularly vulnerable to sonar
exposures. Further investigation is
needed to further assess the potential
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validity of these hypotheses. More
information regarding hypotheses that
attempt to explain how behavioral
responses to non-impulsive sources can
lead to strandings is included in the
Stranding and Mortality section.
Acoustic Masking
Marine mammals use acoustic signals
for a variety of purposes, which differ
among species, but include
communication between individuals,
navigation, foraging, reproduction, and
learning about their environment (Erbe
and Farmer, 2000; Tyack, 2000).
Masking, or auditory interference,
generally occurs when sounds in the
environment are louder than and of a
similar frequency to, auditory signals an
animal is trying to receive. Masking is
a phenomenon that affects animals that
are trying to receive acoustic
information about their environment,
including sounds from other members
of their species, predators, prey, and
sounds that allow them to orient in their
environment. Masking these acoustic
signals can disturb the behavior of
individual animals, groups of animals,
or entire populations.
The extent of the masking interference
depends on the spectral, temporal, and
spatial relationships between the signals
an animal is trying to receive and the
masking noise, in addition to other
factors. In humans, significant masking
of tonal signals occurs as a result of
exposure to noise in a narrow band of
similar frequencies. As the sound level
increases, though, the detection of
frequencies above those of the masking
stimulus decreases also. This principle
is expected to apply to marine mammals
as well because of common
biomechanical cochlear properties
across taxa.
Richardson et al. (1995b) argued that
the maximum radius of influence of an
industrial noise (including broadband
low-frequency sound transmission) on a
marine mammal is the distance from the
source to the point at which the noise
can barely be heard. This range is
determined by either the hearing
sensitivity of the animal or the
background noise level present.
Industrial masking is most likely to
affect some species’ ability to detect
communication calls and natural
sounds (i.e., surf noise, prey noise, etc.;
Richardson et al., 1995).
The echolocation calls of toothed
whales are subject to masking by highfrequency sound. Human data indicate
low-frequency sound can mask highfrequency sounds (i.e., upward
masking). Studies on captive
odontocetes by Au et al. (1974, 1985,
1993) indicate that some species may
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use various processes to reduce masking
effects (e.g., adjustments in echolocation
call intensity or frequency as a function
of background noise conditions). There
is also evidence that the directional
hearing abilities of odontocetes are
useful in reducing masking at the highfrequencies these cetaceans use to
echolocate, but not at the low-tomoderate frequencies they use to
communicate (Zaitseva et al., 1980). A
recent study by Nachtigall and Supin
(2008) showed that false killer whales
adjust their hearing to compensate for
ambient sounds and the intensity of
returning echolocation signals.
The functional hearing ranges of
mysticetes, odontocetes, and pinnipeds
underwater all encompass the
frequencies of the sonar sources used in
the Navy’s low-frequency (LF)/MFAS/
HFAS training exercises. Additionally,
almost all species’ vocal repertoires
span across the frequencies of these
sonar sources used by the Navy. The
closer the characteristics of the masking
signal to the signal of interest, the more
likely masking is to occur. For hullmounted sonar, which accounts for a
large number of the takes of marine
mammals (because of the source
strength and number of hours it is
conducted), the pulse length and low
duty cycle of the MFAS/HFAS signal
makes it less likely that masking would
occur as a result.
Impaired Communication
In addition to making it more difficult
for animals to perceive acoustic cues in
their environment, anthropogenic sound
presents separate challenges for animals
that are vocalizing. When they vocalize,
animals are aware of environmental
conditions that affect the ‘‘active space’’
of their vocalizations, which is the
maximum area within which their
vocalizations can be detected before it
drops to the level of ambient noise
(Brenowitz, 2004; Brumm et al., 2004;
Lohr et al., 2003). Animals are also
aware of environmental conditions that
affect whether listeners can discriminate
and recognize their vocalizations from
other sounds, which is more important
than simply detecting that a
vocalization is occurring (Brenowitz,
1982; Brumm et al., 2004; Dooling,
2004, Marten and Marler, 1977;
Patricelli et al., 2006). Most animals that
vocalize have evolved with an ability to
make adjustments to their vocalizations
to increase the signal-to-noise ratio,
active space, and recognizability/
distinguishability of their vocalizations
in the face of temporary changes in
background noise (Brumm et al., 2004;
Patricelli et al., 2006). Vocalizing
animals can make adjustments to
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vocalization characteristics such as the
frequency structure, amplitude,
temporal structure, and temporal
delivery.
Many animals will combine several of
these strategies to compensate for high
levels of background noise.
Anthropogenic sounds that reduce the
signal-to-noise ratio of animal
vocalizations, increase the masked
auditory thresholds of animals listening
for such vocalizations, or reduce the
active space of an animal’s vocalizations
impair communication between
animals. Most animals that vocalize
have evolved strategies to compensate
for the effects of short-term or temporary
increases in background or ambient
noise on their songs or calls. Although
the fitness consequences of these vocal
adjustments remain unknown, like most
other trade-offs animals must make,
some of these strategies probably come
at a cost (Patricelli et al., 2006). For
example, vocalizing more loudly in
noisy environments may have energetic
costs that decrease the net benefits of
vocal adjustment and alter a bird’s
energy budget (Brumm, 2004; Wood and
Yezerinac, 2006). Shifting songs and
calls to higher frequencies may also
impose energetic costs (Lambrechts,
1996).
Stress Responses
Classic stress responses begin when
an animal’s central nervous system
perceives a potential threat to its
homeostasis. That perception triggers
stress responses regardless of whether a
stimulus actually threatens the animal;
the mere perception of a threat is
sufficient to trigger a stress response
(Moberg, 2000; Sapolsky et al., 2005;
Seyle, 1950). Once an animal’s central
nervous system perceives a threat, it
mounts a biological response or defense
that consists of a combination of the
four general biological defense
responses: Behavioral responses,
autonomic nervous system responses,
neuroendocrine responses, or immune
responses.
In the case of many stressors, an
animal’s first and sometimes most
economical (in terms of biotic costs)
response is behavioral avoidance of the
potential stressor or avoidance of
continued exposure to a stressor. An
animal’s second line of defense to
stressors involves the sympathetic part
of the autonomic nervous system and
the classical ‘‘fight or flight’’ response
which includes the cardiovascular
system, the gastrointestinal system, the
exocrine glands, and the adrenal
medulla to produce changes in heart
rate, blood pressure, and gastrointestinal
activity that humans commonly
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associate with ‘‘stress.’’ These responses
have a relatively short duration and may
or may not have significant long-term
effect on an animal’s welfare.
An animal’s third line of defense to
stressors involves its neuroendocrine
systems; the system that has received
the most study has been the
hypothalmus-pituitary-adrenal system
(also known as the HPA axis in
mammals or the hypothalamuspituitary-interrenal axis in fish and
some reptiles). Unlike stress responses
associated with the autonomic nervous
system, virtually all neuro-endocrine
functions that are affected by stress—
including immune competence,
reproduction, metabolism, and
behavior—are regulated by pituitary
hormones. Stress-induced changes in
the secretion of pituitary hormones have
been implicated in failed reproduction
(Moberg, 1987; Rivier, 1995), altered
metabolism (Elasser et al., 2000),
reduced immune competence (Blecha,
2000), and behavioral disturbance.
Increases in the circulation of
glucocorticosteroids (cortisol,
corticosterone, and aldosterone in
marine mammals; see Romano et al.,
2004) have been equated with stress for
many years.
The primary distinction between
stress (which is adaptive and does not
normally place an animal at risk) and
distress is the biotic cost of the
response. During a stress response, an
animal uses glycogen stores that can be
quickly replenished once the stress is
alleviated. In such circumstances, the
cost of the stress response would not
pose a risk to the animal’s welfare.
However, when an animal does not have
sufficient energy reserves to satisfy the
energetic costs of a stress response,
energy resources must be diverted from
other biotic function, which impairs
those functions that experience the
diversion. For example, when mounting
a stress response diverts energy away
from growth in young animals, those
animals may experience stunted growth.
When mounting a stress response
diverts energy from a fetus, an animal’s
reproductive success and its fitness will
suffer. In these cases, the animals will
have entered a pre-pathological or
pathological state which is called
‘‘distress’’ (Seyle, 1950) or ‘‘allostatic
loading’’ (McEwen and Wingfield,
2003). This pathological state will last
until the animal replenishes its biotic
reserves sufficient to restore normal
function. Note that these examples
involved a long-term (days or weeks)
stress response exposure to stimuli.
Relationships between these
physiological mechanisms, animal
behavior, and the costs of stress
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responses have also been documented
fairly well through controlled
experiments; because this physiology
exists in every vertebrate that has been
studied, it is not surprising that stress
responses and their costs have been
documented in both laboratory and freeliving animals (for examples see,
Holberton et al., 1996; Hood et al., 1998;
Jessop et al., 2003; Krausman et al.,
2004; Lankford et al., 2005; Reneerkens
et al., 2002; Thompson and Hamer,
2000). Information has also been
collected on the physiological responses
of marine mammals to exposure to
anthropogenic sounds (Fair and Becker,
2000; Romano et al., 2002; Wright et al.,
2008). Various efforts have been
undertaken to investigate the impact
from vessels (both whale-watching and
general vessel traffic noise), and
demonstrated impacts do occur (Bain,
2002; Erbe, 2002; Noren et al., 2009;
Williams et al., 2006, 2009, 2014a,
2014b; Read et al., 2014; Rolland et al.,
2012; Pirotta et al., 2015). This body of
research for the most part has
investigated impacts associated with the
presence of chronic stressors, which
differ significantly from the proposed
Navy training activities in the GOA
TMAA. For example, in an analysis of
energy costs to killer whales, Williams
et al. (2009) suggested that whalewatching in Canada’s Johnstone Strait
resulted in lost feeding opportunities
due to vessel disturbance, which could
carry higher costs than other measures
of behavioral change might suggest.
Ayres et al. (2012) recently reported on
research in the Salish Sea (Washington
state) involving the measurement of
southern resident killer whale fecal
hormones to assess two potential threats
to the species recovery: Lack of prey
(salmon) and impacts to behavior from
vessel traffic. Ayres et al. (2012)
suggested that the lack of prey
overshadowed any population-level
physiological impacts on southern
resident killer whales from vessel
traffic. Rolland et al. (2012) found that
noise reduction from reduced ship
traffic in the Bay of Fundy was
associated with decreased stress in
North Atlantic right whales. In a
conceptual model developed by the
Population Consequences of Acoustic
Disturbance (PCAD) working group,
serum hormones were identified as
possible indicators of behavioral effects
that are translated into altered rates of
reproduction and mortality. The Office
of Naval Research hosted a workshop
(Effects of Stress on Marine Mammals
Exposed to Sound) in 2009 that focused
on this very topic (ONR, 2009).
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Studies of other marine animals and
terrestrial animals would also lead us to
expect some marine mammals to
experience physiological stress
responses and, perhaps, physiological
responses that would be classified as
‘‘distress’’ upon exposure to high
frequency, mid-frequency and lowfrequency sounds. For example, Jansen
(1998) reported on the relationship
between acoustic exposures and
physiological responses that are
indicative of stress responses in humans
(for example, elevated respiration and
increased heart rates). Jones (1998)
reported on reductions in human
performance when faced with acute,
repetitive exposures to acoustic
disturbance. Trimper et al. (1998)
reported on the physiological stress
responses of osprey to low-level aircraft
noise while Krausman et al. (2004)
reported on the auditory and
physiological stress responses of
endangered Sonoran pronghorn to
military overflights. Smith et al. (2004a,
2004b), for example, identified noiseinduced physiological transient stress
responses in hearing-specialist fish (i.e.,
goldfish) that accompanied short- and
long-term hearing losses. Welch and
Welch (1970) reported physiological
and behavioral stress responses that
accompanied damage to the inner ears
of fish and several mammals.
Hearing is one of the primary senses
marine mammals use to gather
information about their environment
and to communicate with conspecifics.
Although empirical information on the
relationship between sensory
impairment (TTS, PTS, and acoustic
masking) on marine mammals remains
limited, it seems reasonable to assume
that reducing an animal’s ability to
gather information about its
environment and to communicate with
other members of its species would be
stressful for animals that use hearing as
their primary sensory mechanism.
Therefore, we assume that acoustic
exposures sufficient to trigger onset PTS
or TTS would be accompanied by
physiological stress responses because
terrestrial animals exhibit those
responses under similar conditions
(NRC, 2003). More importantly, marine
mammals might experience stress
responses at received levels lower than
those necessary to trigger onset TTS.
Based on empirical studies of the time
required to recover from stress
responses (Moberg, 2000), we also
assume that stress responses are likely
to persist beyond the time interval
required for animals to recover from
TTS and might result in pathological
and pre-pathological states that would
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Behavioral Disturbance
Behavioral responses to sound are
highly variable and context-specific.
Many different variables can influence
an animal’s perception of and response
to (nature and magnitude) an acoustic
event. An animal’s prior experience
with a sound or sound source affects
whether it is less likely (habituation) or
more likely (sensitization) to respond to
certain sounds in the future (animals
can also be innately pre-disposed to
respond to certain sounds in certain
ways) (Southall et al., 2007). Related to
the sound itself, the perceived nearness
of the sound, bearing of the sound
(approaching vs. retreating), similarity
of a sound to biologically relevant
sounds in the animal’s environment
(i.e., calls of predators, prey, or
conspecifics), and familiarity of the
sound may affect the way an animal
responds to the sound (Southall et al.,
2007). Individuals (of different age,
gender, reproductive status, etc.) among
most populations will have variable
hearing capabilities, and differing
behavioral sensitivities to sounds that
will be affected by prior conditioning,
experience, and current activities of
those individuals. Often, specific
acoustic features of the sound and
contextual variables (i.e., proximity,
duration, or recurrence of the sound or
the current behavior that the marine
mammal is engaged in or its prior
experience), as well as entirely separate
factors such as the physical presence of
a nearby vessel, may be more relevant
to the animal’s response than the
received level alone. Ellison et al. (2012)
outlined an approach to assessing the
effects of sound on marine mammals
that incorporates contextual-based
factors. They recommend considering
not just the received level of sound, but
also the activity the animal is engaged
in at the time the sound is received, the
nature and novelty of the sound (i.e., is
this a new sound from the animal’s
perspective), and the distance between
the sound source and the animal. They
submit that this ‘‘exposure context,’’ as
described, greatly influences the type of
behavioral response exhibited by the
animal. This sort of contextual
information is challenging to predict
with accuracy for ongoing activities that
occur over large scales and large periods
of time. While contextual elements of
this sort are typically not included in
calculations to quantify take, they are
often considered qualitatively (where
supporting information is available) in
the subsequent analysis that seeks to
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assess the likely consequences of sound
exposures above a certain level.
Exposure of marine mammals to
sound sources can result in no response
or responses including, but not limited
to: Increased alertness; orientation or
attraction to a sound source; vocal
modifications; cessation of feeding;
cessation of social interaction; alteration
of movement or diving behavior; habitat
abandonment (temporary or permanent);
and, in severe cases, panic, flight,
stampede, or stranding, potentially
resulting in death (Southall et al., 2007).
A review of marine mammal responses
to anthropogenic sound was first
conducted by Richardson and others in
1995. More recent reviews (Nowacek et
al., 2007; Ellison et al., 2012) address
studies conducted since 1995 and
focuses on observations where the
received sound level of the exposed
marine mammal(s) was known or could
be estimated. The following subsections provide examples of behavioral
responses that provide an idea of the
variability in behavioral responses that
would be expected given the differential
sensitivities of marine mammal species
to sound and the wide range of potential
acoustic sources to which a marine
mammal may be exposed. Estimates of
the types of behavioral responses that
could occur for a given sound exposure
should be determined from the
literature that is available for each
species, or extrapolated from closely
related species when no information
exists.
Flight Response—A flight response is
a dramatic change in normal movement
to a directed and rapid movement away
from the perceived location of a sound
source. Relatively little information on
flight responses of marine mammals to
anthropogenic signals exist, although
observations of flight responses to the
presence of predators have occurred
(Connor and Heithaus, 1996). Flight
responses have been speculated as being
a component of marine mammal
strandings associated with sonar
activities (Evans and England, 2001).
Response to Predator—Evidence
suggests that at least some marine
mammals have the ability to
acoustically identify potential predators.
For example, harbor seals that reside in
the coastal waters off British Columbia
are frequently targeted by certain groups
of killer whales, but not others. The
seals discriminate between the calls of
threatening and non-threatening killer
whales (Deecke et al., 2002), a capability
that should increase survivorship while
reducing the energy required for
attending to and responding to all killer
whale calls. The occurrence of masking
or hearing impairment provides a means
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by which marine mammals may be
prevented from responding to the
acoustic cues produced by their
predators. Whether or not this is a
possibility depends on the duration of
the masking/hearing impairment and
the likelihood of encountering a
predator during the time that predator
cues are impeded.
Diving—Changes in dive behavior can
vary widely. They may consist of
increased or decreased dive times and
surface intervals as well as changes in
the rates of ascent and descent during a
dive. Variations in dive behavior may
reflect interruptions in biologically
significant activities (e.g., foraging) or
they may be of little biological
significance. Variations in dive behavior
may also expose an animal to
potentially harmful conditions (e.g.,
increasing the chance of ship-strike) or
may serve as an avoidance response that
enhances survivorship. The impact of a
variation in diving resulting from an
acoustic exposure depends on what the
animal is doing at the time of the
exposure and the type and magnitude of
the response.
Nowacek et al. (2004) reported
disruptions of dive behaviors in foraging
North Atlantic right whales when
exposed to an alerting stimulus, an
action, they noted, that could lead to an
increased likelihood of ship strike.
However, the whales did not respond to
playbacks of either right whale social
sounds or vessel noise, highlighting the
importance of the sound characteristics
in producing a behavioral reaction.
Conversely, Indo-Pacific humpback
dolphins have been observed to dive for
longer periods of time in areas where
vessels were present and/or
approaching (Ng and Leung, 2003). In
both of these studies, the influence of
the sound exposure cannot be
decoupled from the physical presence of
a surface vessel, thus complicating
interpretations of the relative
contribution of each stimulus to the
response. Indeed, the presence of
surface vessels, their approach, and
speed of approach, seemed to be
significant factors in the response of the
Indo-Pacific humpback dolphins (Ng
and Leung, 2003). Low frequency
signals of the Acoustic Thermometry of
Ocean Climate (ATOC) sound source
were not found to affect dive times of
humpback whales in Hawaiian waters
(Frankel and Clark, 2000) or to overtly
affect elephant seal dives (Costa et al.,
2003). They did, however, produce
subtle effects that varied in direction
and degree among the individual seals,
illustrating the equivocal nature of
behavioral effects and consequent
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difficulty in defining and predicting
them.
Due to past incidents of beaked whale
strandings associated with sonar
operations, feedback paths are provided
between avoidance and diving and
indirect tissue effects. This feedback
accounts for the hypothesis that
variations in diving behavior and/or
avoidance responses can possibly result
in nitrogen tissue supersaturation and
nitrogen off-gassing, possibly to the
point of deleterious vascular bubble
formation (Jepson et al., 2003).
Although hypothetical, discussions
surrounding this potential process are
controversial.
Foraging—Disruption of feeding
behavior can be difficult to correlate
with anthropogenic sound exposure, so
it is usually inferred by observed
displacement from known foraging
areas, the appearance of secondary
indicators (e.g., bubble nets or sediment
plumes), or changes in dive behavior.
Noise from seismic surveys was not
found to impact the feeding behavior in
western grey whales off the coast of
Russia (Yazvenko et al., 2007) and
sperm whales engaged in foraging dives
did not abandon dives when exposed to
distant signatures of seismic airguns
(Madsen et al., 2006). However, Miller
et al. (2009) reported buzz rates (a proxy
for feeding) 19 percent lower during
exposure to distant signatures of seismic
airguns. Balaenopterid whales exposed
to moderate low-frequency signals
similar to the ATOC sound source
demonstrated no variation in foraging
activity (Croll et al., 2001), whereas five
out of six North Atlantic right whales
exposed to an acoustic alarm
interrupted their foraging dives
(Nowacek et al., 2004). Although the
received sound pressure levels were
similar in the latter two studies, the
frequency, duration, and temporal
pattern of signal presentation were
different. These factors, as well as
differences in species sensitivity, are
likely contributing factors to the
differential response. Blue whales
exposed to simulated mid-frequency
sonar in the Southern California Bight
were less likely to produce low
frequency calls usually associated with
´
feeding behavior (Melcon et al., 2012).
However, Melcon et al. (2012) were
unable to determine if suppression of
low frequency calls reflected a change
in their feeding performance or
abandonment of foraging behavior and
indicated that implications of the
documented responses are unknown.
Further, it is not known whether the
lower rates of calling actually indicated
a reduction in feeding behavior or social
contact since the study used data from
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remotely deployed, passive acoustic
monitoring buoys. In contrast, blue
whales increased their likelihood of
calling when ship noise was present,
and decreased their likelihood of calling
in the presence of explosive noise,
although this result was not statistically
´
significant (Melcon et al., 2012).
Additionally, the likelihood of an
animal calling decreased with the
increased received level of midfrequency sonar, beginning at a SPL of
approximately 110–120 dB re 1 mPa
´
(Melcon et al., 2012). Results from the
2010–2011 field season of an ongoing
behavioral response study in Southern
California waters indicated that, in some
cases and at low received levels, tagged
blue whales responded to midfrequency sonar but that those responses
were mild and there was a quick return
to their baseline activity (Southall et al.,
2011; Southall et al., 2012b). A
determination of whether foraging
disruptions incur fitness consequences
will require information on or estimates
of the energetic requirements of the
individuals and the relationship
between prey availability, foraging effort
and success, and the life history stage of
the animal. Goldbogen et al., (2013)
monitored behavioral responses of
tagged blue whales located in feeding
areas when exposed simulated MFA
sonar. Responses varied depending on
behavioral context, with deep feeding
whales being more significantly affected
(i.e., generalized avoidance; cessation of
feeding; increased swimming speeds; or
directed travel away from the source)
compared to surface feeding individuals
that typically showed no change in
behavior. Non-feeding whales also
seemed to be affected by exposure. The
authors indicate that disruption of
feeding and displacement could impact
individual fitness and health. However,
for this to be true, we would have to
assume that an individual whale could
not compensate for this lost feeding
opportunity by either immediately
feeding at another location, by feeding
shortly after cessation of acoustic
exposure, or by feeding at a later time.
There is no indication this is the case,
particularly since unconsumed prey
would likely still be available in the
environment in most cases following the
cessation of acoustic exposure.
Breathing—Variations in respiration
naturally vary with different behaviors
and variations in respiration rate as a
function of acoustic exposure can be
expected to co-occur with other
behavioral reactions, such as a flight
response or an alteration in diving.
However, respiration rates in and of
themselves may be representative of
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annoyance or an acute stress response.
Mean exhalation rates of gray whales at
rest and while diving were found to be
unaffected by seismic surveys
conducted adjacent to the whale feeding
grounds (Gailey et al., 2007). Studies
with captive harbor porpoises showed
increased respiration rates upon
introduction of acoustic alarms
(Kastelein et al., 2001; Kastelein et al.,
2006a) and emissions for underwater
data transmission (Kastelein et al.,
2005). However, exposure of the same
acoustic alarm to a striped dolphin
under the same conditions did not elicit
a response (Kastelein et al., 2006a),
again highlighting the importance in
understanding species differences in the
tolerance of underwater noise when
determining the potential for impacts
resulting from anthropogenic sound
exposure.
Social Relationships—Social
interactions between mammals can be
affected by noise via the disruption of
communication signals or by the
displacement of individuals. Disruption
of social relationships therefore depends
on the disruption of other behaviors
(e.g., caused avoidance, masking, etc.)
and no specific overview is provided
here. However, social disruptions must
be considered in context of the
relationships that are affected. Longterm disruptions of mother/calf pairs or
mating displays have the potential to
affect the growth and survival or
reproductive effort/success of
individuals, respectively.
Vocalizations (also see Masking
Section)—Vocal changes in response to
anthropogenic noise can occur across
the repertoire of sound production
modes used by marine mammals, such
as whistling, echolocation click
production, calling, and singing.
Changes may result in response to a
need to compete with an increase in
background noise or may reflect an
increased vigilance or startle response.
For example, in the presence of lowfrequency active sonar, humpback
whales have been observed to increase
the length of their ’’songs’’ (Miller et al.,
2000; Fristrup et al., 2003), possibly due
to the overlap in frequencies between
the whale song and the low-frequency
active sonar. A similar compensatory
effect for the presence of low-frequency
vessel noise has been suggested for right
whales; right whales have been
observed to shift the frequency content
of their calls upward while reducing the
rate of calling in areas of increased
anthropogenic noise (Parks et al., 2007;
Roland et al., 2012). Killer whales off
the northwestern coast of the U.S. have
been observed to increase the duration
of primary calls once a threshold in
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observing vessel density (e.g., whale
watching) was reached, which has been
suggested as a response to increased
masking noise produced by the vessels
(Foote et al., 2004; NOAA, 2014b). In
contrast, both sperm and pilot whales
potentially ceased sound production
during the Heard Island feasibility test
(Bowles et al., 1994), although it cannot
be absolutely determined whether the
inability to acoustically detect the
animals was due to the cessation of
sound production or the displacement
of animals from the area.
Avoidance—Avoidance is the
displacement of an individual from an
area as a result of the presence of a
sound. Richardson et al. (1995) noted
that avoidance reactions are the most
obvious manifestations of disturbance in
marine mammals. It is qualitatively
different from the flight response, but
also differs in the magnitude of the
response (i.e., directed movement, rate
of travel, etc.). Oftentimes avoidance is
temporary, and animals return to the
area once the noise has ceased. Longer
term displacement is possible, however,
which can lead to changes in abundance
or distribution patterns of the species in
the affected region if they do not
become acclimated to the presence of
the sound (Blackwell et al., 2004; Bejder
et al., 2006; Teilmann et al., 2006).
Acute avoidance responses have been
observed in captive porpoises and
pinnipeds exposed to a number of
different sound sources (Kastelein et al.,
2001; Finneran et al., 2003; Kastelein et
al., 2006a; Kastelein et al., 2006b).
Short-term avoidance of seismic
surveys, low frequency emissions, and
acoustic deterrents have also been noted
in wild populations of odontocetes
(Bowles et al., 1994; Goold, 1996; 1998;
Stone et al., 2000; Morton and
Symonds, 2002) and to some extent in
mysticetes (Gailey et al., 2007), while
longer term or repetitive/chronic
displacement for some dolphin groups
and for manatees has been suggested to
be due to the presence of chronic vessel
noise (Haviland-Howell et al., 2007;
Miksis-Olds et al., 2007).
Maybaum (1993) conducted sound
playback experiments to assess the
effects of MFAS on humpback whales in
Hawaiian waters. Specifically, she
exposed focal pods to sounds of a 3.3kHz sonar pulse, a sonar frequency
sweep from 3.1 to 3.6 kHz, and a control
(blank) tape while monitoring behavior,
movement, and underwater
vocalizations. The two types of sonar
signals (which both contained mid- and
low-frequency components) differed in
their effects on the humpback whales,
but both resulted in avoidance behavior.
The whales responded to the pulse by
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increasing their distance from the sound
source and responded to the frequency
sweep by increasing their swimming
speeds and track linearity. In the
Caribbean, sperm whales avoided
exposure to mid-frequency submarine
sonar pulses, in the range of 1000 Hz to
10,000 Hz (IWC 2005).
Kvadsheim et al. (2007) conducted a
controlled exposure experiment in
which killer whales fitted with D-tags
were exposed to mid-frequency active
sonar (Source A: A 1.0 second upsweep
209 dB @ 1–2 kHz every 10 seconds for
10 minutes; Source B: With a 1.0 second
upsweep 197 dB @ 6–7 kHz every 10
seconds for 10 minutes). When exposed
to Source A, a tagged whale and the
group it was traveling with did not
appear to avoid the source. When
exposed to Source B, the tagged whales
along with other whales that had been
carousel feeding, ceased feeding during
the approach of the sonar and moved
rapidly away from the source. When
exposed to Source B, Kvadsheim and
his co-workers reported that a tagged
killer whale seemed to try to avoid
further exposure to the sound field by
the following behaviors: Immediately
swimming away (horizontally) from the
source of the sound; engaging in a series
of erratic and frequently deep dives that
seemed to take it below the sound field;
or swimming away while engaged in a
series of erratic and frequently deep
dives. Although the sample sizes in this
study are too small to support statistical
analysis, the behavioral responses of the
killer whales were consistent with the
results of other studies.
In 2007, the first in a series of
behavioral response studies, a
collaboration by the Navy, NMFS, and
other scientists showed one beaked
whale (Mesoplodon densirostris)
responding to an MFAS playback. Tyack
et al. (2011) indicates that the playback
began when the tagged beaked whale
was vocalizing at depth (at the deepest
part of a typical feeding dive), following
a previous control with no sound
exposure. The whale appeared to stop
clicking significantly earlier than usual,
when exposed to mid-frequency signals
in the 130–140 dB (rms) received level
range. After a few more minutes of the
playback, when the received level
reached a maximum of 140–150 dB, the
whale ascended on the slow side of
normal ascent rates with a longer than
normal ascent, at which point the
exposure was terminated. The results
are from a single experiment and a
greater sample size is needed before
robust and definitive conclusions can be
drawn.
Tyack et al. (2011) also indicates that
Blainville’s beaked whales appear to be
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sensitive to noise at levels well below
expected TTS (∼160 dB re1mPa). This
sensitivity is manifest by an adaptive
movement away from a sound source.
This response was observed irrespective
of whether the signal transmitted was
within the band width of MFAS, which
suggests that beaked whales may not
respond to the specific sound
signatures. Instead, they may be
sensitive to any pulsed sound from a
point source in this frequency range.
The response to such stimuli appears to
involve maximizing the distance from
the sound source.
Stimpert et al. (2014) tagged a Baird’s
beaked whale, which was subsequently
exposed to simulated MFAS. Received
levels of sonar on the tag increased to
a maximum of 138 dB re 1mPa, which
occurred during the first exposure dive.
Some sonar received levels could not be
measured due to flow noise and surface
noise on the tag.
Results from a 2007–2008 study
conducted near the Bahamas showed a
change in diving behavior of an adult
Blainville’s beaked whale to playback of
MFAS and predator sounds (Boyd et al.,
2008; Southall et al. 2009; Tyack et al.,
2011). Reaction to mid-frequency
sounds included premature cessation of
clicking and termination of a foraging
dive, and a slower ascent rate to the
surface. Results from a similar
behavioral response study in southern
California waters have been presented
for the 2010–2011 field season (Southall
et al. 2011; DeRuiter et al., 2013b).
DeRuiter et al. (2013b) presented results
from two Cuvier’s beaked whales that
were tagged and exposed to simulated
MFAS during the 2010 and 2011 field
seasons of the southern California
behavioral response study. The 2011
whale was also incidentally exposed to
MFAS from a distant naval exercise.
Received levels from the MFAS signals
from the controlled and incidental
exposures were calculated as 84–144
and 78–106 dB re 1 mPa root mean
square (rms), respectively. Both whales
showed responses to the controlled
exposures, ranging from initial
orientation changes to avoidance
responses characterized by energetic
fluking and swimming away from the
source. However, the authors did not
detect similar responses to incidental
exposure to distant naval sonar
exercises at comparable received levels,
indicating that context of the exposures
(e.g., source proximity, controlled
source ramp-up) may have been a
significant factor. Specifically, this
result suggests that caution is needed
when using marine mammal response
data collected from smaller, nearer
sound sources to predict at what
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received levels animals may repond to
larger sound sources that are
significantly farther away—as the
distance of the source appears to be an
important contextual variable and
animals may be less responsive to
sources at notably greater distances.
Cuvier’s beaked whale responses
suggested particular sensitivity to sound
exposure as consistent with results for
Blainville’s beaked whale. Similarly,
beaked whales exposed to sonar during
British training exercises stopped
foraging (DSTL, 2007), and preliminary
results of controlled playback of sonar
may indicate feeding/foraging
disruption of killer whales and sperm
whales (Miller et al., 2011).
In the 2007–2008 Bahamas study,
playback sounds of a potential
predator—a killer whale—resulted in a
similar but more pronounced reaction,
which included longer inter-dive
intervals and a sustained straight-line
departure of more than 20 km from the
area (Boyd et al., 2008; Southall et al.
2009; Tyack et al., 2011). The authors
noted, however, that the magnified
reaction to the predator sounds could
represent a cumulative effect of
exposure to the two sound types since
killer whale playback began
approximately 2 hours after midfrequency source playback. Pilot whales
and killer whales off Norway also
exhibited horizontal avoidance of a
transducer with outputs in the midfrequency range (signals in the 1–2 kHz
and 6–7 kHz ranges) (Miller et al., 2011).
Additionally, separation of a calf from
its group during exposure to MFAS
playback was observed on one occasion
(Miller et al., 2011; 2012). Miller et al.
(2012) noted that this single observed
mother-calf separation was unusual for
several reasons, including the fact that
the experiment was conducted in an
unusually narrow fjord roughly 1 km
wide and that the sonar exposure was
started unusually close to the pod
including the calf. Both of these factors
could have contributed to calf
separation. In contrast, preliminary
analyses suggest that none of the pilot
whales or false killer whales in the
Bahamas showed an avoidance response
to controlled exposure playbacks
(Southall et al., 2009).
Through analysis of the behavioral
response studies, a preliminary
overarching effect of greater sensitivity
to all anthropogenic exposures was seen
in beaked whales compared to the other
odontocetes studied (Southall et al.,
2009). Therefore, recent studies have
focused specifically on beaked whale
responses to active sonar transmissions
or controlled exposure playback of
simulated sonar on various military
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ranges (Defence Science and
Technology Laboratory, 2007; Claridge
and Durban, 2009; Moretti et al., 2009;
McCarthy et al., 2011; Miller et al.,
2012; Southall et al., 2011, 2012a,
2012b, 2013, 2014; Tyack et al., 2011).
In the Bahamas, Blainville’s beaked
whales located on the range will move
off-range during sonar use and return
only after the sonar transmissions have
stopped, sometimes taking several days
to do so (Claridge and Durban 2009;
Moretti et al., 2009; McCarthy et al.,
2011; Tyack et al., 2011). Moretti et al.
(2014) used recordings from seafloormounted hydrophones at the Atlantic
Undersea Test and Evaluation Center
(AUTEC) to analyze the probability of
Blainsville’s beaked whale dives before,
during, and after Navy sonar exercises.
Orientation—A shift in an animal’s
resting state or an attentional change via
an orienting response represent
behaviors that would be considered
mild disruptions if occurring alone. As
previously mentioned, the responses
may co-occur with other behaviors; for
instance, an animal may initially orient
toward a sound source, and then move
away from it. Thus, any orienting
response should be considered in
context of other reactions that may
occur.
Behavioral Responses
Southall et al. (2007) reports the
results of the efforts of a panel of experts
in acoustic research from behavioral,
physiological, and physical disciplines
that convened and reviewed the
available literature on marine mammal
hearing and physiological and
behavioral responses to human-made
sound with the goal of proposing
exposure criteria for certain effects. This
peer-reviewed compilation of literature
is very valuable, though Southall et al.
(2007) note that not all data are equal,
some have poor statistical power,
insufficient controls, and/or limited
information on received levels,
background noise, and other potentially
important contextual variables—such
data were reviewed and sometimes used
for qualitative illustration but were not
included in the quantitative analysis for
the criteria recommendations. All of the
studies considered, however, contain an
estimate of the received sound level
when the animal exhibited the indicated
response.
In the Southall et al. (2007)
publication, for the purposes of
analyzing responses of marine mammals
to anthropogenic sound and developing
criteria, the authors differentiate
between single pulse sounds, multiple
pulse sounds, and non-pulse sounds.
MFAS/HFAS sonar is considered a non-
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pulse sound. Southall et al. (2007)
summarize the studies associated with
low-frequency, mid-frequency, and
high-frequency cetacean and pinniped
responses to non-pulse sounds, based
strictly on received level, in Appendix
C of their article (incorporated by
reference and summarized in the three
paragraphs below).
The studies that address responses of
low-frequency cetaceans to non-pulse
sounds include data gathered in the
field and related to several types of
sound sources (of varying similarity to
MFAS/HFAS) including: Vessel noise,
drilling and machinery playback, lowfrequency M-sequences (sine wave with
multiple phase reversals) playback,
tactical low-frequency active sonar
playback, drill ships, Acoustic
Thermometry of Ocean Climate (ATOC)
source, and non-pulse playbacks. These
studies generally indicate no (or very
limited) responses to received levels in
the 90 to 120 dB re: 1 mPa range and an
increasing likelihood of avoidance and
other behavioral effects in the 120 to
160 dB range. As mentioned earlier,
though, contextual variables play a very
important role in the reported responses
and the severity of effects are not linear
when compared to received level. Also,
few of the laboratory or field datasets
had common conditions, behavioral
contexts or sound sources, so it is not
surprising that responses differ.
The studies that address responses of
mid-frequency cetaceans to non-pulse
sounds include data gathered both in
the field and the laboratory and related
to several different sound sources (of
varying similarity to MFAS/HFAS)
including: Pingers, drilling playbacks,
ship and ice-breaking noise, vessel
noise, Acoustic Harassment Devices
(AHDs), Acoustic Deterrent Devices
(ADDs), MFAS, and non-pulse bands
and tones. Southall et al. (2007) were
unable to come to a clear conclusion
regarding the results of these studies. In
some cases, animals in the field showed
significant responses to received levels
between 90 and 120 dB, while in other
cases these responses were not seen in
the 120 to 150 dB range. The disparity
in results was likely due to contextual
variation and the differences between
the results in the field and laboratory
data (animals typically responded at
lower levels in the field).
The studies that address responses of
high-frequency cetaceans to non-pulse
sounds include data gathered both in
the field and the laboratory and related
to several different sound sources (of
varying similarity to MFAS/HFAS)
including: Pingers, AHDs, and various
laboratory non-pulse sounds. All of
these data were collected from harbor
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porpoises. Southall et al. (2007)
concluded that the existing data
indicate that harbor porpoises are likely
sensitive to a wide range of
anthropogenic sounds at low received
levels (∼ 90 to 120 dB), at least for initial
exposures. All recorded exposures
above 140 dB induced profound and
sustained avoidance behavior in wild
harbor porpoises (Southall et al., 2007).
Rapid habituation was noted in some
but not all studies. There is no data to
indicate whether other high frequency
cetaceans are as sensitive to
anthropogenic sound as harbor
porpoises.
The studies that address the responses
of pinnipeds in water to non-impulsive
sounds include data gathered both in
the field and the laboratory and related
to several different sound sources (of
varying similarity to MFAS/HFAS)
including: AHDs, ATOC, various nonpulse sounds used in underwater data
communication, underwater drilling,
and construction noise. Few studies
exist with enough information to
include them in the analysis. The
limited data suggested that exposures to
non-pulse sounds between 90 and 140
dB generally do not result in strong
behavioral responses in pinnipeds in
water, but no data exist at higher
received levels.
Potential Effects of Behavioral
Disturbance
The different ways that marine
mammals respond to sound are
sometimes indicators of the ultimate
effect that exposure to a given stimulus
will have on the well-being (survival,
reproduction, etc.) of an animal. There
is limited marine mammal data
quantitatively relating the exposure of
marine mammals to sound to effects on
reproduction or survival, though data
exists for terrestrial species to which we
can draw comparisons for marine
mammals.
Attention is the cognitive process of
selectively concentrating on one aspect
of an animal’s environment while
ignoring other things (Posner, 1994).
Because animals (including humans)
have limited cognitive resources, there
is a limit to how much sensory
information they can process at any
time. The phenomenon called
‘‘attentional capture’’ occurs when a
stimulus (usually a stimulus that an
animal is not concentrating on or
attending to) ‘‘captures’’ an animal’s
attention. This shift in attention can
occur consciously or subconsciously
(for example, when an animal hears
sounds that it associates with the
approach of a predator) and the shift in
attention can be sudden (Dukas, 2002;
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van Rij, 2007). Once a stimulus has
captured an animal’s attention, the
animal can respond by ignoring the
stimulus, assuming a ‘‘watch and wait’’
posture, or treat the stimulus as a
disturbance and respond accordingly,
which includes scanning for the source
of the stimulus or ‘‘vigilance’’
(Cowlishaw et al., 2004).
Vigilance is normally an adaptive
behavior that helps animals determine
the presence or absence of predators,
assess their distance from conspecifics,
or to attend cues from prey (Bednekoff
and Lima, 1998; Treves, 2000). Despite
those benefits, however, vigilance has a
cost of time; when animals focus their
attention on specific environmental
cues, they are not attending to other
activities such as foraging. These costs
have been documented best in foraging
animals, where vigilance has been
shown to substantially reduce feeding
rates (Saino, 1994; Beauchamp and
Livoreil, 1997; Fritz et al., 2002).
Animals will spend more time being
vigilant, which may translate to less
time foraging or resting, when
disturbance stimuli approach them
more directly, remain at closer
distances, have a greater group size (for
example, multiple surface vessels), or
when they co-occur with times that an
animal perceives increased risk (for
example, when they are giving birth or
accompanied by a calf). Most of the
published literature, however, suggests
that direct approaches will increase the
amount of time animals will dedicate to
being vigilant. For example, bighorn
sheep and Dall’s sheep dedicated more
time being vigilant, and less time resting
or foraging, when aircraft made direct
approaches over them (Frid, 2001;
Stockwell et al., 1991).
Several authors have established that
long-term and intense disturbance
stimuli can cause population declines
by reducing the body condition of
individuals that have been disturbed,
followed by reduced reproductive
success, reduced survival, or both (Daan
et al., 1996; Madsen, 1994; White,
1983). For example, Madsen (1994)
reported that pink-footed geese in
undisturbed habitat gained body mass
and had about a 46-percent reproductive
success rate compared with geese in
disturbed habitat (being consistently
scared off the fields on which they were
foraging) which did not gain mass and
had a 17-percent reproductive success
rate. Similar reductions in reproductive
success have been reported for mule
deer disturbed by all-terrain vehicles
(Yarmoloy et al., 1988), caribou
disturbed by seismic exploration blasts
(Bradshaw et al., 1998), caribou
disturbed by low-elevation military jet-
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9969
fights (Luick et al., 1996), and caribou
disturbed by low-elevation jet flights
(Harrington and Veitch, 1992).
Similarly, a study of elk that were
disturbed experimentally by pedestrians
concluded that the ratio of young to
mothers was inversely related to
disturbance rate (Phillips and
Alldredge, 2000).
The primary mechanism by which
increased vigilance and disturbance
appear to affect the fitness of individual
animals is by disrupting an animal’s
time budget and, as a result, reducing
the time they might spend foraging and
resting (which increases an animal’s
activity rate and energy demand). For
example, a study of grizzly bears
reported that bears disturbed by hikers
reduced their energy intake by an
average of 12 kcal/minute (50.2 x 103kJ/
minute), and spent energy fleeing or
acting aggressively toward hikers (White
et al. 1999). Alternately, Ridgway et al.
(2006) reported that increased vigilance
in bottlenose dolphins exposed to sound
over a 5-day period did not cause any
sleep deprivation or stress effects such
as changes in cortisol or epinephrine
levels.
Lusseau and Bejder (2007) present
data from three long-term studies
illustrating the connections between
disturbance from whale-watching boats
and population-level effects in
cetaceans. In Sharks Bay Australia, the
abundance of bottlenose dolphins was
compared within adjacent control and
tourism sites over three consecutive 4.5year periods of increasing tourism
levels. Between the second and third
time periods, in which tourism doubled,
dolphin abundance decreased by 15
percent in the tourism area and did not
change significantly in the control area.
In Fiordland, New Zealand, two
populations (Milford and Doubtful
Sounds) of bottlenose dolphins with
tourism levels that differed by a factor
of seven were observed and significant
increases in travelling time and
decreases in resting time were
documented for both. Consistent shortterm avoidance strategies were observed
in response to tour boats until a
threshold of disturbance was reached
(average 68 minutes between
interactions), after which the response
switched to a longer term habitat
displacement strategy. For one
population tourism only occurred in a
part of the home range, however,
tourism occurred throughout the home
range of the Doubtful Sound population
and once boat traffic increased beyond
the 68-minute threshold (resulting in
abandonment of their home range/
preferred habitat), reproductive success
drastically decreased (increased
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stillbirths) and abundance decreased
significantly (from 67 to 56 individuals
in short period). Last, in a study of
northern resident killer whales off
Vancouver Island, exposure to boat
traffic was shown to reduce foraging
opportunities and increase traveling
time. A simple bioenergetics model was
applied to show that the reduced
foraging opportunities equated to a
decreased energy intake of 18 percent,
while the increased traveling incurred
an increased energy output of 3–4
percent, which suggests that a
management action based on avoiding
interference with foraging might be
particularly effective.
On a related note, many animals
perform vital functions, such as feeding,
resting, traveling, and socializing, on a
diel cycle (24-hour cycle). Substantive
behavioral reactions to noise exposure
(such as disruption of critical life
functions, displacement, or avoidance of
important habitat) are more likely to be
significant if they last more than one
diel cycle or recur on subsequent days
(Southall et al., 2007). Consequently, a
behavioral response lasting less than 1
day and not recurring on subsequent
days is not considered particularly
severe unless it could directly affect
reproduction or survival (Southall et al.,
2007). Note that there is a difference
between multiple-day substantive
behavioral reactions and multiple-day
anthropogenic activities. For example,
just because an at-sea exercises last for
multiple days does not necessarily mean
that individual animals are either
exposed to those exercises for multiple
days or, further, exposed in a manner
resulting in a sustained multiple day
substantive behavioral responses.
In order to understand how the effects
of activities may or may not impact
stocks and populations of marine
mammals, it is necessary to understand
not only what the likely disturbances
are going to be, but how those
disturbances may affect the
reproductive success and survivorship
of individuals, and then how those
impacts to individuals translate to
population changes. Following on the
earlier work of a committee of the U.S.
National Research Council (NRC, 2005),
New et al. (2014), in an effort termed the
Potential Consequences of Disturbance
(PCoD), outline an updated conceptual
model of the relationships linking
disturbance to changes in behavior and
physiology, health, vital rates, and
population dynamics (below). As
depicted, behavioral and physiological
changes can either have direct (acute)
effects on vital rates, such as when
changes in habitat use or increased
stress levels raise the probability of
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the continental U.S. and Alaska (NMFS,
2011).
Several sources have published lists
of mass stranding events of cetaceans in
an attempt to identify relationships
between those stranding events and
military sonar (Hildebrand, 2004; IWC,
2005; Taylor et al., 2004). For example,
based on a review of stranding records
between 1960 and 1995, the
International Whaling Commission
(2005) identified ten mass stranding
events of Cuvier’s beaked whales had
been reported and one mass stranding of
four Baird’s beaked whale. The IWC
concluded that, out of eight stranding
events reported from the mid-1980s to
the summer of 2003, seven had been
coincident with the use of tactical midfrequency sonar, one of those seven had
been associated with the use of tactical
low-frequency sonar, and the remaining
stranding event had been associated
with the use of seismic airguns.
Stranding and Mortality
Most of the stranding events reviewed
When a live or dead marine mammal
swims or floats onto shore and becomes by the International Whaling
‘‘beached’’ or incapable of returning to
Commission involved beaked whales. A
sea, the event is termed a ‘‘stranding’’
mass stranding of Cuvier’s beaked
(Geraci et al., 1999; Perrin and Geraci,
whales in the eastern Mediterranean Sea
2002; Geraci and Lounsbury, 2005;
occurred in 1996 (Frantzis, 1998) and
NMFS, 2007). The legal definition for a
mass stranding events involving
stranding within the U.S. can be found
Gervais’ beaked whales, Blainville’s
in section 410 of the MMPA (16 U.S.C.
beaked whales, and Cuvier’s beaked
1421h).
whales occurred off the coast of the
Marine mammals are known to strand
Canary Islands in the late 1980s
for a variety of reasons, such as
(Simmonds and Lopez-Jurado, 1991).
infectious agents, biotoxicosis,
The stranding events that occurred in
starvation, fishery interaction, ship
the Canary Islands and Kyparissiakos
strike, unusual oceanographic or
Gulf in the late 1990s and the Bahamas
weather events, sound exposure, or
in 2000 have been the most intensivelycombinations of these stressors
studied mass stranding events and have
sustained concurrently or in series.
been associated with naval maneuvers
However, the cause or causes of most
involving the use of tactical sonar.
strandings are unknown (Geraci et al.,
1976; Eaton, 1979, Odell et al., 1980;
Between 1960 and 2006, 48 strandings
Best, 1982). Numerous studies suggest
(68 percent) involved beaked whales,
that the physiology, behavior, habitat
three (4 percent) involved dolphins, and
relationships, age, or condition of
14 (20 percent) involved whale species.
cetaceans may cause them to strand or
Cuvier’s beaked whales were involved
might pre-dispose them to strand when
in the greatest number of these events
exposed to another phenomenon. These
(48 or 68 percent), followed by sperm
suggestions are consistent with the
whales (seven or 10 percent), and
conclusions of numerous other studies
Blainville’s and Gervais’ beaked whales
that have demonstrated that
(four each or 6 percent). Naval activities
combinations of dissimilar stressors
(not just activities conducted by the U.S.
commonly combine to kill an animal or
Navy) that might have involved active
dramatically reduce its fitness, even
sonar are reported to have coincided
though one exposure without the other
with nine or 10 (13 to 14 percent) of
does not produce the same result
those stranding events. Between the
(Chroussos, 2000; Creel, 2005; DeVries
et al., 2003; Fair and Becker, 2000; Foley mid-1980s and 2003 (the period
reported by the International Whaling
et al., 2001; Moberg, 2000; Relyea,
Commission), NMFS identified reports
2005a; 2005b, Romero, 2004; Sih et al.,
of 44 mass cetacean stranding events of
2004). For reference, between 2001 and
which at least seven were coincident
2009, there was an annual average of
with naval exercises that were using
1,400 cetacean strandings and 4,300
pinniped strandings along the coasts of
MFAS.
mother-calf separation or predation, or
they can have indirect and long-term
(chronic) effects on vital rates, such as
when changes in time/energy budgets or
increased disease susceptibility affect
health, which then affects vital rates
(New et al., 2014). In addition to
outlining this general framework and
compiling the relevant literature that
supports it, New et al. (2014) have
chosen four example species for which
extensive long-term monitoring data
exist (southern elephant seals, North
Atlantic right whales, Ziphidae beaked
whales, and bottlenose dolphins) and
developed state-space energetic models
that can be used to effectively forecast
longer-term, population-level impacts
from behavioral changes. While these
are very specific models with very
specific data requirements that cannot
yet be applied broadly to projectspecific risk assessments, they are a
critical first step.
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Strandings Associated With Impulsive
Sound
Silver Strand—During a Navy training
event on March 4, 2011 at the Silver
Strand Training Complex in San Diego,
California, three or possibly four
dolphins were killed in an explosion.
During an underwater detonation
training event, a pod of 100 to 150 longbeaked common dolphins were
observed moving towards the 700-yd
(640.1-m) exclusion zone around the
explosive charge, monitored by
personnel in a safety boat and
participants in a dive boat.
Approximately 5 minutes remained on
a time-delay fuse connected to a single
8.76 lb (3.97 kg) explosive charge (C–4
and detonation cord). Although the dive
boat was placed between the pod and
the explosive in an effort to guide the
dolphins away from the area, that effort
was unsuccessful and three long-beaked
common dolphins near the explosion
died. In addition to the three dolphins
found dead on March 4, the remains of
a fourth dolphin were discovered on
March 7, 2011 near Ocean Beach,
California (3 days later and
approximately 11.8 mi. [19 km] from
Silver Strand where the training event
occurred), which might also have been
related to this event. Association of the
fourth stranding with the training event
is uncertain because dolphins strand on
a regular basis in the San Diego area.
Details such as the dolphins’ depth and
distance from the explosive at the time
of the detonation could not be estimated
from the 250 yd (228.6 m) standoff point
of the observers in the dive boat or the
safety boat.
These dolphin mortalities are the only
known occurrence of a U.S. Navy
training or testing event involving
impulsive energy (underwater
detonation) that caused mortality or
injury to a marine mammal (of note, the
time-delay firing underwater explosive
training activity implicated in the
March 4 incident is not proposed for the
training activities in the GOA Study
Area). Despite this being a rare
occurrence, the Navy has reviewed
training requirements, safety
procedures, and possible mitigation
measures and implemented changes to
reduce the potential for this to occur in
the future. Discussions of procedures
associated with underwater explosives
training and other training events are
presented in the Proposed Mitigation
section.
Kyle of Durness, Scotland—On July
22, 2011 a mass stranding event
involving long-finned pilot whales
occurred at Kyle of Durness, Scotland.
An investigation by Brownlow et al.
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(2015) considered unexploded ordnance
detonation activities at a Ministry of
Defense bombing range, conducted by
the Royal Navy prior to and during the
strandings, as a plausible contributing
factor in the mass stranding event.
While Brownlow et al. (2015) concluded
that the serial detonations of underwater
ordnance were an influential factor in
the mass stranding event (along with
presence of a potentially compromised
animal and navigational error in a
topographically complex region) they
also suggest that mitigation measures—
which included observations from a
zodiac only and by personnel not
experienced in marine mammal
observation, among other deficiencies—
were likely insufficient to assess if
cetaceans were in the vicinity of the
detonations. The authors also cite
information from the Ministry of
Defense indicating ‘‘an extraordinarily
high level of activity’’ (i.e., frequency
and intensity of underwater explosions)
on the range in the days leading up to
the stranding.
Strandings Associated With MFAS
Over the past 16 years, there have
been five stranding events coincident
with military mid-frequency sonar use
in which exposure to sonar is believed
to have been a contributing factor:
Greece (1996); the Bahamas (2000);
Madeira (2000); Canary Islands (2002);
and Spain (2006). Additionally, in 2004,
during the Rim of the Pacific (RIMPAC)
exercises, between 150 and 200 usually
pelagic melon-headed whales occupied
the shallow waters of Hanalei Bay,
Kauai, Hawaii for over 28 hours. NMFS
determined that MFAS was a plausible,
if not likely, contributing factor in what
may have been a confluence of events
that led to the stranding. A number of
other stranding events coincident with
the operation of mid-frequency sonar,
including the death of beaked whales or
other species (minke whales, dwarf
sperm whales, pilot whales), have been
reported; however, the majority have
not been investigated to the degree
necessary to determine the cause of the
stranding and only one of these
stranding events, the Bahamas (2000),
was associated with exercises
conducted by the U.S. Navy. Most
recently, the Independent Scientific
Review Panel investigating potential
contributing factors to a 2008 mass
stranding of melon-headed whales in
Antsohihy, Madagascar released its final
report suggesting that the stranding was
likely initially triggered by an industry
seismic survey. This report suggests that
the operation of a commercial highpowered 12 kHz multi-beam
echosounder during an industry seismic
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survey was a plausible and likely initial
trigger that caused a large group of
melon-headed whales to leave their
typical habitat and then ultimately
strand as a result of secondary factors
such as malnourishment and
dehydration. The report indicates that
the risk of this particular convergence of
factors and ultimate outcome is likely
very low, but recommends that the
potential be considered in
environmental planning. Because of the
association between tactical midfrequency active sonar use and a small
number of marine mammal strandings,
the Navy and NMFS have been
considering and addressing the
potential for strandings in association
with Navy activities for years. In
addition to a suite of mitigation
intended to more broadly minimize
impacts to marine mammals, the Navy
and NMFS have a detailed Stranding
Response Plan that outlines reporting,
communication, and response protocols
intended both to minimize the impacts
of, and enhance the analysis of, any
potential stranding in areas where the
Navy operates.
Greece (1996)—Twelve Cuvier’s
beaked whales stranded atypically (in
both time and space) along a 38.2-km
strand of the Kyparissiakos Gulf coast
on May 12 and 13, 1996 (Frantzis,
1998). From May 11 through May 15,
the North Atlantic Treaty Organization
(NATO) research vessel Alliance was
conducting sonar tests with signals of
600 Hz and 3 kHz and source levels of
228 and 226 dB re: 1mPa, respectively
(D’Amico and Verboom, 1998; D’Spain
et al., 2006). The timing and location of
the testing encompassed the time and
location of the strandings (Frantzis,
1998).
Necropsies of eight of the animals
were performed but were limited to
basic external examination and
sampling of stomach contents, blood,
and skin. No ears or organs were
collected, and no histological samples
were preserved. No apparent
abnormalities or wounds were found.
Examination of photos of the animals,
taken soon after their death, revealed
that the eyes of at least four of the
individuals were bleeding. Photos were
taken soon after their death (Frantzis,
2004). Stomach contents contained the
flesh of cephalopods, indicating that
feeding had recently taken place
(Frantzis, 1998).
All available information regarding
the conditions associated with this
stranding event were compiled, and
many potential causes were examined
including major pollution events,
prominent tectonic activity, unusual
physical or meteorological events,
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magnetic anomalies, epizootics, and
conventional military activities
(International Council for the
Exploration of the Sea, 2005a).
However, none of these potential causes
coincided in time or space with the
mass stranding, or could explain its
characteristics (International Council for
the Exploration of the Sea, 2005a). The
robust condition of the animals, plus the
recent stomach contents, is inconsistent
with pathogenic causes. In addition,
environmental causes can be ruled out
as there were no unusual environmental
circumstances or events before or during
this time period and within the general
proximity (Frantzis, 2004).
Because of the rarity of this mass
stranding of Cuvier’s beaked whales in
the Kyparissiakos Gulf (first one in
history), the probability for the two
events (the military exercises and the
strandings) to coincide in time and
location, while being independent of
each other, was thought to be extremely
low (Frantzis, 1998). However, because
full necropsies had not been conducted,
and no abnormalities were noted, the
cause of the strandings could not be
precisely determined (Cox et al., 2006).
A Bioacoustics Panel convened by
NATO concluded that the evidence
available did not allow them to accept
or reject sonar exposures as a causal
agent in these stranding events. The
analysis of this stranding event
provided support for, but no clear
evidence for, the cause-and-effect
relationship of tactical sonar training
activities and beaked whale strandings
(Cox et al., 2006).
Bahamas (2000)—NMFS and the
Navy prepared a joint report addressing
the multi-species stranding in the
Bahamas in 2000, which took place
within 24 hours of U.S. Navy ships
using MFAS as they passed through the
Northeast and Northwest Providence
Channels on March 15–16, 2000. The
ships, which operated both AN/SQS–
53C and AN/SQS–56, moved through
the channel while emitting sonar pings
approximately every 24 seconds. Of the
17 cetaceans that stranded over a 36-hr
period (Cuvier’s beaked whales,
Blainville’s beaked whales, minke
whales, and a spotted dolphin), seven
animals died on the beach (five Cuvier’s
beaked whales, one Blainville’s beaked
whale, and the spotted dolphin), while
the other 10 were returned to the water
alive (though their ultimate fate is
unknown). As discussed in the Bahamas
report (DOC/DON, 2001), there is no
likely association between the minke
whale and spotted dolphin strandings
and the operation of MFAS.
Necropsies were performed on five of
the stranded beaked whales. All five
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necropsied beaked whales were in good
body condition, showing no signs of
infection, disease, ship strike, blunt
trauma, or fishery related injuries, and
three still had food remains in their
stomachs. Auditory structural damage
was discovered in four of the whales,
specifically bloody effusions or
hemorrhaging around the ears. Bilateral
intracochlear and unilateral temporal
region subarachnoid hemorrhage, with
blood clots in the lateral ventricles,
were found in two of the whales. Three
of the whales had small hemorrhages in
their acoustic fats (located along the jaw
and in the melon).
A comprehensive investigation was
conducted and all possible causes of the
stranding event were considered,
whether they seemed likely at the outset
or not. Based on the way in which the
strandings coincided with ongoing
naval activity involving tactical MFAS
use, in terms of both time and
geography, the nature of the
physiological effects experienced by the
dead animals, and the absence of any
other acoustic sources, the investigation
team concluded that MFAS aboard U.S.
Navy ships that were in use during the
active sonar exercise in question were
the most plausible source of this
acoustic or impulse trauma to beaked
whales. This sound source was active in
a complex environment that included
the presence of a surface duct, unusual
and steep bathymetry, a constricted
channel with limited egress, intensive
use of multiple, active sonar units over
an extended period of time, and the
presence of beaked whales that appear
to be sensitive to the frequencies
produced by these active sonars. The
investigation team concluded that the
cause of this stranding event was the
confluence of the Navy MFAS and these
contributory factors working together,
and further recommended that the Navy
avoid operating MFAS in situations
where these five factors would be likely
to occur. This report does not conclude
that all five of these factors must be
present for a stranding to occur, nor that
beaked whales are the only species that
could potentially be affected by the
confluence of the other factors. Based on
this, NMFS believes that the operation
of MFAS in situations where surface
ducts exist, or in marine environments
defined by steep bathymetry and/or
constricted channels may increase the
likelihood of producing a sound field
with the potential to cause cetaceans
(especially beaked whales) to strand,
and therefore, suggests the need for
increased vigilance while operating
MFAS in these areas, especially when
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beaked whales (or potentially other
deep divers) are likely present.
Madeira, Spain (2000)—From May
10–14, 2000, three Cuvier’s beaked
whales were found atypically stranded
on two islands in the Madeira
archipelago, Portugal (Cox et al., 2006).
A fourth animal was reported floating in
the Madeiran waters by fisherman but
did not come ashore (Woods Hole
Oceanographic Institution, 2005). Joint
NATO amphibious training
peacekeeping exercises involving
participants from 17 countries 80
warships, took place in Portugal during
May 2–15, 2000.
The bodies of the three stranded
whales were examined post mortem
(Woods Hole Oceanographic Institution,
2005), though only one of the stranded
whales was fresh enough (24 hours after
stranding) to be necropsied (Cox et al.,
2006). Results from the necropsy
revealed evidence of hemorrhage and
congestion in the right lung and both
kidneys (Cox et al., 2006). There was
also evidence of intercochlear and
intracranial hemorrhage similar to that
which was observed in the whales that
stranded in the Bahamas event (Cox et
al., 2006). There were no signs of blunt
trauma, and no major fractures (Woods
Hole Oceanographic Institution, 2005).
The cranial sinuses and airways were
found to be clear with little or no fluid
deposition, which may indicate good
preservation of tissues (Woods Hole
Oceanographic Institution, 2005).
Several observations on the Madeira
stranded beaked whales, such as the
pattern of injury to the auditory system,
are the same as those observed in the
Bahamas strandings. Blood in and
around the eyes, kidney lesions, pleural
hemorrhages, and congestion in the
lungs are particularly consistent with
the pathologies from the whales
stranded in the Bahamas, and are
consistent with stress and pressure
related trauma. The similarities in
pathology and stranding patterns
between these two events suggest that a
similar pressure event may have
precipitated or contributed to the
strandings at both sites (Woods Hole
Oceanographic Institution, 2005).
Even though no definitive causal link
can be made between the stranding
event and naval exercises, certain
conditions may have existed in the
exercise area that, in their aggregate,
may have contributed to the marine
mammal strandings (Freitas, 2004):
Exercises were conducted in areas of at
least 547 fathoms (1,000 m) depth near
a shoreline where there is a rapid
change in bathymetry on the order of
547 to 3,281 fathoms (1,000 to 6,000 m)
occurring across a relatively short
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horizontal distance (Freitas, 2004);
multiple ships were operating around
Madeira, though it is not known if
MFAS was used, and the specifics of the
sound sources used are unknown (Cox
et al., 2006, Freitas, 2004); and exercises
took place in an area surrounded by
landmasses separated by less than 35
nm (65 km) and at least 10 nm (19 km)
in length, or in an embayment. Exercises
involving multiple ships employing
MFAS near land may produce sound
directed towards a channel or
embayment that may cut off the lines of
egress for marine mammals (Freitas,
2004).
Canary Islands, Spain (2002)—The
southeastern area within the Canary
Islands is well known for aggregations
of beaked whales due to its ocean
depths of greater than 547 fathoms
(1,000 m) within a few hundred meters
of the coastline (Fernandez et al., 2005).
On September 24, 2002, 14 beaked
whales were found stranded on
Fuerteventura and Lanzarote Islands in
the Canary Islands (International
Council for Exploration of the Sea,
2005a). Seven whales died, while the
remaining seven live whales were
returned to deeper waters (Fernandez et
al., 2005). Four beaked whales were
found stranded dead over the next three
days either on the coast or floating
offshore. These strandings occurred
within near proximity of an
international naval exercise that utilized
MFAS and involved numerous surface
warships and several submarines.
Strandings began about 4 hours after the
onset of MFAS activity (International
Council for Exploration of the Sea,
2005a; Fernandez et al., 2005).
Eight Cuvier’s beaked whales, one
Blainville’s beaked whale, and one
Gervais’ beaked whale were necropsied,
six of them within 12 hours of stranding
(Fernandez et al., 2005). No pathogenic
bacteria were isolated from the carcasses
(Jepson et al., 2003). The animals
displayed severe vascular congestion
and hemorrhage especially around the
tissues in the jaw, ears, brain, and
kidneys, displaying marked
disseminated microvascular
hemorrhages associated with
widespread fat emboli (Jepson et al.,
2003; International Council for
Exploration of the Sea, 2005a). Several
organs contained intravascular bubbles,
although definitive evidence of gas
embolism in vivo is difficult to
determine after death (Jepson et al.,
2003). The livers of the necropsied
animals were the most consistently
affected organ, which contained
macroscopic gas-filled cavities and had
variable degrees of fibrotic
encapsulation. In some animals,
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cavitary lesions had extensively
replaced the normal tissue (Jepson et al.,
2003). Stomachs contained a large
amount of fresh and undigested
contents, suggesting a rapid onset of
disease and death (Fernandez et al.,
2005). Head and neck lymph nodes
were enlarged and congested, and
parasites were found in the kidneys of
all animals (Fernandez et al., 2005).
The association of NATO MFAS use
close in space and time to the beaked
whale strandings, and the similarity
between this stranding event and
previous beaked whale mass strandings
coincident with sonar use, suggests that
a similar scenario and causative
mechanism of stranding may be shared
between the events. Beaked whales
stranded in this event demonstrated
brain and auditory system injuries,
hemorrhages, and congestion in
multiple organs, similar to the
pathological findings of the Bahamas
and Madeira stranding events. In
addition, the necropsy results of Canary
Islands stranding event lead to the
hypothesis that the presence of
disseminated and widespread gas
bubbles and fat emboli were indicative
of nitrogen bubble formation, similar to
what might be expected in
decompression sickness (Jepson et al.,
´
2003; Fernandez et al., 2005).
Hanalei Bay (2004)—On July 3 and 4,
2004, approximately 150 to 200 melonheaded whales occupied the shallow
waters of the Hanalei Bay, Kaua’i,
Hawaii for over 28 hrs. Attendees of a
canoe blessing observed the animals
entering the Bay in a single wave
formation at 7 a.m. on July 3, 2004. The
animals were observed moving back
into the shore from the mouth of the Bay
at 9 a.m. The usually pelagic animals
milled in the shallow bay and were
returned to deeper water with human
assistance beginning at 9:30 a.m. on July
4, 2004, and were out of sight by 10:30
a.m.
Only one animal, a calf, was known
to have died following this event. The
animal was noted alive and alone in the
Bay on the afternoon of July 4, 2004,
and was found dead in the Bay the
morning of July 5, 2004. A full
necropsy, magnetic resonance imaging,
and computerized tomography
examination were performed on the calf
to determine the manner and cause of
death. The combination of imaging,
necropsy and histological analyses
found no evidence of infectious,
internal traumatic, congenital, or toxic
factors. Cause of death could not be
definitively determined, but it is likely
that maternal separation, poor
nutritional condition, and dehydration
contributed to the final demise of the
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animal. Although it is not known when
the calf was separated from its mother,
the animals’ movement into the Bay and
subsequent milling and re-grouping may
have contributed to the separation or
lack of nursing, especially if the
maternal bond was weak or this was an
inexperienced mother with her first calf.
Environmental factors, abiotic and
biotic, were analyzed for any anomalous
occurrences that would have
contributed to the animals entering and
remaining in Hanalei Bay. The Bay’s
bathymetry is similar to many other
sites within the Hawaiian Island chain
and dissimilar to sites that have been
associated with mass strandings in other
parts of the U.S. The weather conditions
appeared to be normal for that time of
year with no fronts or other significant
features noted. There was no evidence
of unusual distribution, occurrence of
predator or prey species, or unusual
harmful algal blooms, although Mobley
et al. (2007) suggested that the full moon
cycle that occurred at that time may
have influenced a run of squid into the
Bay. Weather patterns and bathymetry
that have been associated with mass
strandings elsewhere were not found to
occur in this instance.
The Hanalei event was spatially and
temporally correlated with RIMPAC.
Official sonar training and tracking
exercises in the Pacific Missile Range
Facility (PMRF) warning area did not
commence until approximately 8 a.m.
on July 3 and were thus ruled out as a
possible trigger for the initial movement
into the Bay. However, six naval surface
vessels transiting to the operational area
on July 2 intermittently transmitted
active sonar (for approximately 9 hours
total from 1:15 p.m. to 12:30 a.m.) as
they approached from the south. The
potential for these transmissions to have
triggered the whales’ movement into
Hanalei Bay was investigated. Analyses
with the information available indicated
that animals to the south and east of
Kaua’i could have detected active sonar
transmissions on July 2, and reached
Hanalei Bay on or before 7 a.m. on July
3. However, data limitations regarding
the position of the whales prior to their
arrival in the Bay, the magnitude of
sonar exposure, behavioral responses of
melon-headed whales to acoustic
stimuli, and other possible relevant
factors preclude a conclusive finding
regarding the role of sonar in triggering
this event. Propagation modeling
suggests that transmissions from sonar
use during the July 3 exercise in the
PMRF warning area may have been
detectable at the mouth of the Bay. If the
animals responded negatively to these
signals, it may have contributed to their
continued presence in the Bay. The U.S.
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Navy ceased all active sonar
transmissions during exercises in this
range on the afternoon of July 3.
Subsequent to the cessation of sonar
use, the animals were herded out of the
Bay.
While causation of this stranding
event may never be unequivocally
determined, NMFS consider the active
sonar transmissions of July 2–3, 2004, a
plausible, if not likely, contributing
factor in what may have been a
confluence of events. This conclusion is
based on the following: (1) The
evidently anomalous nature of the
stranding; (2) its close spatiotemporal
correlation with wide-scale, sustained
use of sonar systems previously
associated with stranding of deep-diving
marine mammals; (3) the directed
movement of two groups of transmitting
vessels toward the southeast and
southwest coast of Kauai; (4) the results
of acoustic propagation modeling and
an analysis of possible animal transit
times to the Bay; and (5) the absence of
any other compelling causative
explanation. The initiation and
persistence of this event may have
resulted from an interaction of
biological and physical factors. The
biological factors may have included the
presence of an apparently uncommon,
deep-diving cetacean species (and
possibly an offshore, non-resident
group), social interactions among the
animals before or after they entered the
Bay, and/or unknown predator or prey
conditions. The physical factors may
have included the presence of nearby
deep water, multiple vessels transiting
in a directed manner while transmitting
active sonar over a sustained period, the
presence of surface sound ducting
conditions, and/or intermittent and
random human interactions while the
animals were in the Bay.
A separate event involving melonheaded whales and rough-toothed
dolphins took place over the same
period of time in the Northern Mariana
Islands (Jefferson et al., 2006), which is
several thousand miles from Hawaii.
Some 500 to 700 melon-headed whales
came into Sasanhaya Bay on July 4,
2004, near the island of Rota and then
left of their own accord after 5.5 hours;
no known active sonar transmissions
occurred in the vicinity of that event.
The Rota incident led to scientific
debate regarding what, if any,
relationship the event had to the
simultaneous events in Hawaii and
whether they might be related by some
common factor (e.g., there was a full
moon on July 2, 2004, as well as during
other melon-headed whale strandings
and nearshore aggregations (Brownell et
al., 2009; Lignon et al., 2007; Mobley et
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al., 2007). Brownell et al. (2009)
compared the two incidents, along with
one other stranding incident at Nuka
Hiva in French Polynesia and normal
resting behaviors observed at Palmyra
Island, in regard to physical features in
the areas, melon-headed whale
behavior, and lunar cycles. Brownell et
al., (2009) concluded that the rapid
entry of the whales into Hanalei Bay,
their movement into very shallow water
far from the 100-m contour, their
milling behavior (typical pre-stranding
behavior), and their reluctance to leave
the bay constituted an unusual event
that was not similar to the events that
occurred at Rota (but was similar to the
events at Palmyra), which appear to be
similar to observations of melon-headed
whales resting normally at Palmyra
Island. Additionally, there was no
correlation between lunar cycle and the
types of behaviors observed in the
Brownell et al. (2009) examples.
Spain (2006)—The Spanish Cetacean
Society reported an atypical mass
stranding of four beaked whales that
occurred January 26, 2006, on the
southeast coast of Spain, near Mojacar
(Gulf of Vera) in the Western
Mediterranean Sea. According to the
report, two of the whales were
discovered the evening of January 26
and were found to be still alive. Two
other whales were discovered during
the day on January 27, but had already
died. The first three animals were
located near the town of Mojacar and
the fourth animal was found dead, a few
kilometers north of the first three
animals. From January 25–26, 2006,
Standing NATO Response Force
Maritime Group Two (five of seven
ships including one U.S. ship under
NATO Operational Control) had
conducted active sonar training against
a Spanish submarine within 50 nm (93
km) of the stranding site.
Veterinary pathologists necropsied
the two male and two female Cuvier’s
beaked whales. According to the
pathologists, the most likely primary
cause of this type of beaked whale mass
stranding event was anthropogenic
acoustic activities, most probably antisubmarine MFAS used during the
military naval exercises. However, no
positive acoustic link was established as
a direct cause of the stranding. Even
though no causal link can be made
between the stranding event and naval
exercises, certain conditions may have
existed in the exercise area that, in their
aggregate, may have contributed to the
marine mammal strandings (Freitas,
2004): Exercises were conducted in
areas of at least 547 fathoms (1,000 m)
depth near a shoreline where there is a
rapid change in bathymetry on the order
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of 547 to 3,281 fathoms (1,000 to 6,000
m) occurring across a relatively short
horizontal distance (Freitas, 2004);
multiple ships (in this instance, five)
were operating MFAS in the same area
over extended periods of time (in this
case, 20 hours) in close proximity; and
exercises took place in an area
surrounded by landmasses, or in an
embayment. Exercises involving
multiple ships employing MFAS near
land may have produced sound directed
towards a channel or embayment that
may have cut off the lines of egress for
the affected marine mammals (Freitas,
2004).
Association Between Mass Stranding
Events and Exposure to MFAS
Several authors have noted
similarities between some of these
stranding incidents: They occurred in
islands or archipelagoes with deep
water nearby, several appeared to have
been associated with acoustic
waveguides like surface ducting, and
the sound fields created by ships
transmitting MFAS (Cox et al., 2006;
D’Spain et al., 2006). Although Cuvier’s
beaked whales have been the most
common species involved in these
stranding events (81 percent of the total
number of stranded animals), other
beaked whales (including Mesoplodon
europeaus, M. densirostris, and
Hyperoodon ampullatus) comprise 14
percent of the total. Other species
(Stenella coeruleoalba, Kogia breviceps
and Balaenoptera acutorostrata) have
stranded, but in much lower numbers
and less consistently than beaked
whales.
Based on the evidence available,
however, NMFS cannot determine
whether (a) Cuvier’s beaked whale is
more prone to injury from high-intensity
sound than other species; (b) their
behavioral responses to sound makes
them more likely to strand; or (c) they
are more likely to be exposed to MFAS
than other cetaceans (for reasons that
remain unknown). Because the
association between active sonar
exposures and marine mammals mass
stranding events is not consistent—
some marine mammals strand without
being exposed to sonar and some sonar
transmissions are not associated with
marine mammal stranding events
despite their co-occurrence—other risk
factors or a grouping of risk factors
probably contribute to these stranding
events.
Behaviorally Mediated Responses to
MFAS That May Lead To Stranding
Although the confluence of Navy
MFAS with the other contributory
factors noted in the report was
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identified as the cause of the 2000
Bahamas stranding event, the specific
mechanisms that led to that stranding
(or the others) are not understood, and
there is uncertainty regarding the
ordering of effects that led to the
stranding. It is unclear whether beaked
whales were directly injured by sound
(e.g., acoustically mediated bubble
growth, as addressed above) prior to
stranding or whether a behavioral
response to sound occurred that
ultimately caused the beaked whales to
be injured and strand.
Although causal relationships
between beaked whale stranding events
and active sonar remain unknown,
several authors have hypothesized that
stranding events involving these species
in the Bahamas and Canary Islands may
have been triggered when the whales
changed their dive behavior in a startled
response to exposure to active sonar or
to further avoid exposure (Cox et al.,
2006; Rommel et al., 2006). These
authors proposed three mechanisms by
which the behavioral responses of
beaked whales upon being exposed to
active sonar might result in a stranding
event. These include the following: Gas
bubble formation caused by excessively
fast surfacing; remaining at the surface
too long when tissues are supersaturated
with nitrogen; or diving prematurely
when extended time at the surface is
necessary to eliminate excess nitrogen.
More specifically, beaked whales that
occur in deep waters that are in close
proximity to shallow waters (for
example, the ‘‘canyon areas’’ that are
cited in the Bahamas stranding event;
see D’Spain and D’Amico, 2006), may
respond to active sonar by swimming
into shallow waters to avoid further
exposures and strand if they were not
able to swim back to deeper waters.
Second, beaked whales exposed to
active sonar might alter their dive
behavior. Changes in their dive behavior
might cause them to remain at the
surface or at depth for extended periods
of time which could lead to hypoxia
directly by increasing their oxygen
demands or indirectly by increasing
their energy expenditures (to remain at
depth) and increase their oxygen
demands as a result. If beaked whales
are at depth when they detect a ping
from an active sonar transmission and
change their dive profile, this could lead
to the formation of significant gas
bubbles, which could damage multiple
organs or interfere with normal
physiological function (Cox et al., 2006;
Rommel et al., 2006; Zimmer and
Tyack, 2007). Baird et al. (2005) found
that slow ascent rates from deep dives
and long periods of time spent within
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50 m of the surface were typical for both
Cuvier’s and Blainville’s beaked whales,
the two species involved in mass
strandings related to naval sonar. These
two behavioral mechanisms may be
necessary to purge excessive dissolved
nitrogen concentrated in their tissues
during their frequent long dives (Baird
et al., 2005). Baird et al. (2005) further
suggests that abnormally rapid ascents
or premature dives in response to highintensity sonar could indirectly result in
physical harm to the beaked whales,
through the mechanisms described
above (gas bubble formation or nonelimination of excess nitrogen).
Because many species of marine
mammals make repetitive and
prolonged dives to great depths, it has
long been assumed that marine
mammals have evolved physiological
mechanisms to protect against the
effects of rapid and repeated
decompressions. Although several
investigators have identified
physiological adaptations that may
protect marine mammals against
nitrogen gas supersaturation (alveolar
collapse and elective circulation;
Kooyman et al., 1972; Ridgway and
Howard, 1979), Ridgway and Howard
(1979) reported that bottlenose dolphins
that were trained to dive repeatedly had
muscle tissues that were substantially
supersaturated with nitrogen gas.
Houser et al. (2001) used these data to
model the accumulation of nitrogen gas
within the muscle tissue of other marine
mammal species and concluded that
cetaceans that dive deep and have slow
ascent or descent speeds would have
tissues that are more supersaturated
with nitrogen gas than other marine
mammals. Based on these data, Cox et
al. (2006) hypothesized that a critical
dive sequence might make beaked
whales more prone to stranding in
response to acoustic exposures. The
sequence began with (1) very deep (to
depths as deep as 2 kilometers) and long
(as long as 90 minutes) foraging dives;
(2) relatively slow, controlled ascents;
and (3) a series of ‘‘bounce’’ dives
between 100 and 400 m in depth (also
see Zimmer and Tyack, 2007). They
concluded that acoustic exposures that
disrupted any part of this dive sequence
(for example, causing beaked whales to
spend more time at surface without the
bounce dives that are necessary to
recover from the deep dive) could
produce excessive levels of nitrogen
supersaturation in their tissues, leading
to gas bubble and emboli formation that
produces pathologies similar to
decompression sickness.
Zimmer and Tyack (2007) modeled
nitrogen tension and bubble growth in
several tissue compartments for several
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hypothetical dive profiles and
concluded that repetitive shallow dives
(defined as a dive where depth does not
exceed the depth of alveolar collapse,
approximately 72 m for Ziphius),
perhaps as a consequence of an
extended avoidance reaction to sonar
sound, could pose a risk for
decompression sickness and that this
risk should increase with the duration
of the response. Their models also
suggested that unrealistically rapid
ascent rates of ascent from normal dive
behaviors are unlikely to result in
supersaturation to the extent that bubble
formation would be expected. Tyack et
al. (2006) suggested that emboli
observed in animals exposed to midfrequency range sonar (Jepson et al.,
´
2003; Fernandez et al., 2005; Fernandez
et al., 2012) could stem from a
behavioral response that involves
repeated dives shallower than the depth
of lung collapse. Given that nitrogen gas
accumulation is a passive process (i.e.
nitrogen is metabolically inert), a
bottlenose dolphin was trained to
repetitively dive a profile predicted to
elevate nitrogen saturation to the point
that nitrogen bubble formation was
predicted to occur. However, inspection
of the vascular system of the dolphin via
ultrasound did not demonstrate the
formation of asymptomatic nitrogen gas
bubbles (Houser et al., 2007). Baird et al.
(2008), in a beaked whale tagging study
off Hawaii, showed that deep dives are
equally common during day or night,
but ‘‘bounce dives’’ are typically a
daytime behavior, possibly associated
with visual predator avoidance. This
may indicate that ‘‘bounce dives’’ are
associated with something other than
behavioral regulation of dissolved
nitrogen levels, which would be
necessary day and night.
If marine mammals respond to a Navy
vessel that is transmitting active sonar
in the same way that they might
respond to a predator, their probability
of flight responses should increase
when they perceive that Navy vessels
are approaching them directly, because
a direct approach may convey detection
and intent to capture (Burger and
Gochfeld, 1981, 1990; Cooper, 1997,
1998). The probability of flight
responses should also increase as
received levels of active sonar increase
(and the ship is, therefore, closer) and
as ship speeds increase (that is, as
approach speeds increase). For example,
the probability of flight responses in
Dall’s sheep (Ovis dalli dalli) (Frid
2001a, b), ringed seals (Phoca hispida)
(Born et al., 1999), Pacific brant (Branta
bernic nigricans) and Canada geese (B.
Canadensis) increased as a helicopter or
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fixed-wing aircraft approached groups
of these animals more directly (Ward et
al., 1999). Bald eagles (Haliaeetus
leucocephalus) perched on trees
alongside a river were also more likely
to flee from a paddle raft when their
perches were closer to the river or were
closer to the ground (Steidl and
Anthony, 1996).
Despite the many theories involving
bubble formation (both as a direct cause
of injury (see Acoustically Mediated
Bubble Growth Section) and an indirect
cause of stranding (See Behaviorally
Mediated Bubble Growth Section),
Southall et al., (2007) summarizes that
there is either scientific disagreement or
a lack of information regarding each of
the following important points: (1)
Received acoustical exposure conditions
for animals involved in stranding
events; (2) pathological interpretation of
observed lesions in stranded marine
mammals; (3) acoustic exposure
conditions required to induce such
physical trauma directly; (4) whether
noise exposure may cause behavioral
reactions (such as atypical diving
behavior) that secondarily cause bubble
formation and tissue damage; and (5)
the extent the post mortem artifacts
introduced by decomposition before
sampling, handling, freezing, or
necropsy procedures affect
interpretation of observed lesions.
Strandings in the GOA TMAA
Northern Edge—Prior to the start of
Northern Edge 2015 (a joint training
exercise in the GOA TMAA hosted by
Alaskan Command) and before Navy
vessels were in the Gulf of Alaska, the
Navy was informed by NMFS of various
marine mammals found dead in the Gulf
of Alaska and that NMFS was
attempting to obtain samples from them.
It has been reported that at least nine
drifting and floating fin whales and
multiple pinniped species were found
in Gulf of Alaska waters as early as May
23, 2015 between Kodiak Island to
Unimak Pass. NMFS is still
investigating these findings but a
possible cause referenced has been an
algal bloom. During Northern Edge
2015, two Navy vessels training in the
Gulf of Alaska on separate days
encountered a well-decayed whale
carcass. This whale or whales may
possibly be the same animal observed
by both ships, and given the stage of
decomposition, might have been one of
the floating whales reported by other
entities to NMFS before Northern Edge
began. The ships followed Navy
reporting procedures and the
information was provided to NMFS to
aid in the investigation. There is no
causal connection with Navy activities
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given the advanced stage of
decomposition and gap of timing of
when Navy maritime training events
began.
Impulsive Sources
Underwater explosive detonations
send a shock wave and sound energy
through the water and can release
gaseous by-products, create an
oscillating bubble, or cause a plume of
water to shoot up from the water
surface. The shock wave and
accompanying noise are of most concern
to marine animals. Depending on the
intensity of the shock wave and size,
location, and depth of the animal, an
animal can be injured, killed, suffer
non-lethal physical effects, experience
hearing related effects with or without
behavioral responses, or exhibit
temporary behavioral responses or
tolerance from hearing the blast sound.
Generally, exposures to higher levels of
impulse and pressure levels would
result in greater impacts to an
individual animal.
Injuries resulting from a shock wave
take place at boundaries between tissues
of different densities. Different
velocities are imparted to tissues of
different densities, and this can lead to
their physical disruption. Blast effects
are greatest at the gas-liquid interface
(Landsberg, 2000). Gas-containing
organs, particularly the lungs and
gastrointestinal tract, are especially
susceptible (Goertner, 1982; Hill, 1978;
Yelverton et al., 1973). In addition, gascontaining organs including the nasal
sacs, larynx, pharynx, trachea, and
lungs may be damaged by compression/
expansion caused by the oscillations of
the blast gas bubble (Reidenberg and
Laitman, 2003). Intestinal walls can
bruise or rupture, with subsequent
hemorrhage and escape of gut contents
into the body cavity. Less severe
gastrointestinal tract injuries include
contusions, petechiae (small red or
purple spots caused by bleeding in the
skin), and slight hemorrhaging
(Yelverton et al., 1973).
Because the ears are the most
sensitive to pressure, they are the organs
most sensitive to injury (Ketten, 2000).
Sound-related damage associated with
sound energy from detonations can be
theoretically distinct from injury from
the shock wave, particularly farther
from the explosion. If a noise is audible
to an animal, it has the potential to
damage the animal’s hearing by causing
decreased sensitivity (Ketten, 1995).
Sound-related trauma can be lethal or
sublethal. Lethal impacts are those that
result in immediate death or serious
debilitation in or near an intense source
and are not, technically, pure acoustic
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trauma (Ketten, 1995). Sublethal
impacts include hearing loss, which is
caused by exposures to perceptible
sounds. Severe damage (from the shock
wave) to the ears includes tympanic
membrane rupture, fracture of the
ossicles, damage to the cochlea,
hemorrhage, and cerebrospinal fluid
leakage into the middle ear. Moderate
injury implies partial hearing loss due
to tympanic membrane rupture and
blood in the middle ear. Permanent
hearing loss also can occur when the
hair cells are damaged by one very loud
event, as well as by prolonged exposure
to a loud noise or chronic exposure to
noise. The level of impact from blasts
depends on both an animal’s location
and, at outer zones, on its sensitivity to
the residual noise (Ketten, 1995).
There have been fewer studies
addressing the behavioral effects of
explosives on marine mammals
compared to MFAS/HFAS. However,
though the nature of the sound waves
emitted from an explosion are different
(in shape and rise time) from MFAS/
HFAS, NMFS still anticipates the same
sorts of behavioral responses to result
from repeated explosive detonations (a
smaller range of likely less severe
responses (i.e., not rising to the level of
MMPA harassment) would be expected
to occur as a result of exposure to a
single explosive detonation that was not
powerful enough or close enough to the
animal to cause TTS or injury).
Baleen whales have shown a variety
of responses to impulse sound sources,
including avoidance, reduced surface
intervals, altered swimming behavior,
and changes in vocalization rates
(Richardson et al., 1995; Gordon et al.,
2003; Southall, 2007). While most
bowhead whales did not show active
avoidance until within 8 km of seismic
vessels (Richardson et al., 1995), some
whales avoided vessels by more than 20
km at received levels as low as 120 dB
re 1 mPa rms. Additionally, Malme et al.
(1988) observed clear changes in diving
and respiration patterns in bowheads at
ranges up to 73 km from seismic vessels,
with received levels as low as 125 dB re
1 mPa.
Gray whales migrating along the U.S.
west coast showed avoidance responses
to seismic vessels by 10 percent of
animals at 164 dB re 1 mPa, and by 90
percent of animals at 190 dB re 1 mPa,
with similar results for whales in the
Bering Sea (Malme 1986, 1988). In
contrast, noise from seismic surveys was
not found to impact feeding behavior or
exhalation rates while resting or diving
in western gray whales off the coast of
Russia (Yazvenko et al., 2007; Gailey et
al., 2007).
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Humpback whales showed avoidance
behavior at ranges of 5–8 km from a
seismic array during observational
studies and controlled exposure
experiments in western Australia
(McCauley, 1998; Todd et al., 1996)
found no clear short-term behavioral
responses by foraging humpbacks to
explosions associated with construction
operations in Newfoundland, but did
see a trend of increased rates of net
entanglement and a shift to a higher
incidence of net entanglement closer to
the noise source.
Seismic pulses at average received
levels of 131 dB re 1 micropascal
squared second (mPa2-s) caused blue
whales to increase call production (Di
Iorio and Clark, 2010). In contrast,
McDonald et al. (1995) tracked a blue
whale with seafloor seismometers and
reported that it stopped vocalizing and
changed its travel direction at a range of
10 km from the seismic vessel
(estimated received level 143 dB re 1
mPa peak-to-peak). These studies
demonstrate that even low levels of
noise received far from the noise source
can induce behavioral responses.
Madsen et al. (2006) and Miller et al.
(2009) tagged and monitored eight
sperm whales in the Gulf of Mexico
exposed to seismic airgun surveys.
Sound sources were from approximately
2 to 7 nm away from the whales and
based on multipath propagation
received levels were as high as 162 dB
SPL re 1 mPa with energy content
greatest between 0.3 and 3.0 kHz
(Madsen, 2006). The whales showed no
horizontal avoidance, although the
whale that was approached most closely
had an extended resting period and did
not resume foraging until the airguns
had ceased firing (Miller et al., 2009).
The remaining whales continued to
execute foraging dives throughout
exposure; however, swimming
movements during foraging dives were
6 percent lower during exposure than
control periods, suggesting subtle effects
of noise on foraging behavior (Miller et
al., 2009). Captive bottlenose dolphins
sometimes vocalized after an exposure
to impulse sound from a seismic
watergun (Finneran et al., 2010a).
A review of behavioral reactions by
pinnipeds to impulse noise can be
found in Richardson et al. (1995) and
Southall et al. (2007). Blackwell et al.
(2004) observed that ringed seals
exhibited little or no reaction to pipedriving noise with mean underwater
levels of 157 dB re 1 mPa rms and in air
levels of 112 dB re 20 mPa, suggesting
that the seals had habituated to the
noise. In contrast, captive California sea
lions avoided sounds from an impulse
source at levels of 165–170 dB re 1 mPa
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(Finneran et al., 2003b). Experimentally,
¨
Gotz and Janik (2011) tested
underwater, startle responses to a
startling sound (sound with a rapid rise
time and a 93 dB sensation level [the
level above the animal’s threshold at
that frequency]) and a non-startling
sound (sound with the same level, but
with a slower rise time) in wildcaptured gray seals. The animals
exposed to the startling treatment
avoided a known food source, whereas
animals exposed to the non-startling
treatment did not react or habituated
during the exposure period. The results
of this study highlight the importance of
the characteristics of the acoustic signal
in an animal’s response of habituation.
Vessels
Ship strikes of cetaceans can cause
major wounds, which may lead to the
death of the animal. An animal at the
surface could be struck directly by a
vessel, a surfacing animal could hit the
bottom of a vessel, or an animal just
below the surface could be cut by a
vessel’s propeller. The severity of
injuries typically depends on the size
and speed of the vessel (Knowlton and
Kraus, 2001; Laist et al., 2001;
Vanderlaan and Taggart, 2007). The
most vulnerable marine mammals are
those that spend extended periods of
time at the surface in order to restore
oxygen levels within their tissues after
deep dives (e.g., the sperm whale). In
addition, some baleen whales, such as
the North Atlantic right whale, seem
generally unresponsive to vessel sound,
making them more susceptible to vessel
collisions (Nowacek et al., 2004). These
species are primarily large, slow moving
whales. Smaller marine mammals (e.g.,
bottlenose dolphin) move quickly
through the water column and are often
seen riding the bow wave of large ships.
Marine mammal responses to vessels
may include avoidance and changes in
dive pattern (NRC, 2003).
An examination of all known ship
strikes from all shipping sources
(civilian and military) indicates vessel
speed is a principal factor in whether a
vessel strike results in death (Knowlton
and Kraus, 2001; Laist et al., 2001;
Jensen and Silber, 2003; Vanderlaan and
Taggart, 2007). In assessing records in
which vessel speed was known, Laist et
al. (2001) found a direct relationship
between the occurrence of a whale
strike and the speed of the vessel
involved in the collision. The authors
concluded that most deaths occurred
when a vessel was traveling in excess of
13 knots.
Jensen and Silber (2003) detailed 292
records of known or probable ship
strikes of all large whale species from
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1975 to 2002. Of these, vessel speed at
the time of collision was reported for 58
cases. Of these cases, 39 (or 67 percent)
resulted in serious injury or death (19 of
those resulted in serious injury as
determined by blood in the water,
propeller gashes or severed tailstock,
and fractured skull, jaw, vertebrae,
hemorrhaging, massive bruising or other
injuries noted during necropsy and 20
resulted in death). Operating speeds of
vessels that struck various species of
large whales ranged from 2 to 51 knots.
The majority (79 percent) of these
strikes occurred at speeds of 13 knots or
greater. The average speed that resulted
in serious injury or death was 18.6
knots. Pace and Silber (2005) found that
the probability of death or serious injury
increased rapidly with increasing vessel
speed. Specifically, the predicted
probability of serious injury or death
increased from 45 to 75 percent as
vessel speed increased from 10 to 14
knots, and exceeded 90 percent at 17
knots. Higher speeds during collisions
result in greater force of impact and also
appear to increase the chance of severe
injuries or death. While modeling
studies have suggested that
hydrodynamic forces pulling whales
toward the vessel hull increase with
increasing speed (Clyne, 1999;
Knowlton et al., 1995), this is
inconsistent with Silber et al. (2010),
which demonstrated that there is no
such relationship (i.e., hydrodynamic
forces are independent of speed).
The Jensen and Silber (2003) report
notes that the database represents a
minimum number of collisions, because
the vast majority probably goes
undetected or unreported. In contrast,
Navy vessels are likely to detect any
strike that does occur, and they are
required to report all ship strikes
involving marine mammals. Overall, the
percentages of Navy traffic relative to
overall large shipping traffic are very
small (on the order of 2 percent).
There are no records of any Navy
vessel strikes to marine mammals
during training or testing activities in
the Study Area. There have been Navy
vessel strikes of large whales in areas
outside the Study Area, such as Hawaii
and Southern California. However, these
areas differ significantly from the Study
Area given that both Hawaii and
Southern California have a much higher
number of Navy vessel activities and
much higher densities of large whales.
Other efforts have been undertaken to
investigate the impact from vessels
(both whale-watching and general vessel
traffic noise) and demonstrated impacts
do occur (Bain, 2002; Erbe, 2002;
Lusseau, 2009; Williams et al., 2006,
2009, 2011b, 2013, 2014a, 2014b; Noren
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et al., 2009; Read et al., 2014; Rolland
et al., 2012; Pirotta et al., 2015). This
body of research for the most part has
investigated impacts associated with the
presence of chronic stressors, which
differ significantly from generally
intermittent Navy training and testing
activities. For example, in an analysis of
energy costs to killer whales, Williams
et al. (2009) suggested that whalewatching in the Johnstone Strait
resulted in lost feeding opportunities
due to vessel disturbance, which could
carry higher costs than other measures
of behavioral change might suggest.
Ayres et al. (2012) recently reported on
research in the Salish Sea involving the
measurement of southern resident killer
whale fecal hormones to assess two
potential threats to the species recovery:
Lack of prey (salmon) and impacts to
behavior from vessel traffic. Ayres et al.
(2012) suggested that the lack of prey
overshadowed any population-level
physiological impacts on southern
resident killer whales from vessel
traffic.
Based on the implementation of Navy
mitigation measures and the low density
of Navy ships in the GOA TMAA,
NMFS has concluded, preliminarily,
that the probability of a ship strike is
very low, especially for dolphins and
porpoises, killer whales, social pelagic
odontocetes and pinnipeds that are
highly visible, and/or comparatively
small and maneuverable. Though more
probable because of their size, NMFS
also believes that the likelihood of a
Navy vessel striking a mysticete or
sperm whale is also low with the
implementation of mitigation measures
and the low density of navy ships in the
Study Area. The Navy did not request
take from a ship strike, and based on our
preliminary determination, NMFS is not
recommending that they modify their
request at this time. However, both
NMFS and the Navy are currently
engaged in a Section 7 consultation
under the ESA, and that consultation
will further inform our final decision.
Proposed Mitigation
Under section 101(a)(5)(A) of the
MMPA, NMFS must set forth the
‘‘permissible methods of taking
pursuant to such activity, and other
means of effecting the least practicable
adverse impact on such species or stock
and its habitat, paying particular
attention to rookeries, mating grounds,
and areas of similar significance.’’
NMFS’ duty under this ‘‘least
practicable adverse impact’’ standard is
to prescribe mitigation reasonably
designed to minimize, to the extent
practicable, any adverse populationlevel impacts, as well as habitat
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impacts. While population-level
impacts are minimized by reducing
impacts on individual marine mammals,
not all takes have a reasonable potential
for translating to population-level
impacts. NMFS’ objective under the
‘‘least practicable adverse impact’’
standard is to design mitigation
targeting those impacts on individual
marine mammals that are reasonably
likely to contribute to adverse
population-level effects.
The NDAA of 2004 amended the
MMPA as it relates to military readiness
activities and the ITA process such that
‘‘least practicable adverse impact’’ shall
include consideration of personnel
safety, practicality of implementation,
and impact on the effectiveness of the
‘‘military readiness activity.’’ The
training and testing activities described
in the Navy’s LOA application are
considered military readiness activities.
In Conservation Council for Hawaii v.
National Marine Fisheries Service, No.
1:13–cv–00684 (D. Hawaii March 31,
2015), the court stated that NMFS
‘‘appear[s] to think that [it] satisf[ies] the
statutory ‘least practicable adverse
impact’ requirement with a ‘negligible
impact’ finding.’’ In light of the court’s
decision, we take this opportunity to
make clear our position that the
‘‘negligible impact’’ and ‘‘least
practicable adverse impact’’
requirements are distinct, even though
the focus of both is on population-level
impacts.
A population-level impact is an
impact on the population numbers
(survival) or growth and reproductive
rates (recruitment) of a particular
marine mammal species or stock. As we
noted in the preamble to our general
MMPA implementing regulations, not
every population-level impact violates
the negligible impact requirement. As
we explained, the negligible impact
standard does not require a finding that
the anticipated take will have ‘‘no
effect’’ on population numbers or
growth rates: ‘‘The statutory standard
does not require that the same recovery
rate be maintained, rather that no
significant effect on annual rates of
recruitment or survival occurs . . .
[T]he key factor is the significance of the
level of impact on rates of recruitment
or survival. Only insignificant impacts
on long-term population levels and
trends can be treated as negligible.’’ See
54 FR 40338, 40341–42 (September 29,
1989). Nevertheless, while insignificant
impacts on population numbers or
growth rates may satisfy the negligible
impact requirement, such impacts still
must be mitigated, to the extent
practicable, under the ‘‘least practicable
adverse impact’’ requirement. Thus, the
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negligible impact and least practicable
adverse impact requirements are clearly
distinct, even though both focus on
population-level effects.
Any mitigation measure(s) prescribed
by NMFS should be able to accomplish,
have a reasonable likelihood of
accomplishing (based on current
science), or contribute to accomplishing
one or more of the general goals listed
below:
a. Avoid or minimize injury or death
of marine mammals wherever possible
(goals b, c, and d may contribute to this
goal).
b. Reduce the numbers of marine
mammals (total number or number at
biologically important time or location)
exposed to received levels of MFAS/
HFAS, underwater detonations, or other
activities expected to result in the take
of marine mammals (this goal may
contribute to a, above, or to reducing
harassment takes only).
c. Reduce the number of times (total
number or number at biologically
important time or location) individuals
would be exposed to received levels of
MFAS/HFAS, underwater detonations,
or other activities expected to result in
the take of marine mammals (this goal
may contribute to a, above, or to
reducing harassment takes only).
d. Reduce the intensity of exposures
(either total number or number at
biologically important time or location)
to received levels of MFAS/HFAS,
underwater detonations, or other
activities expected to result in the take
of marine mammals (this goal may
contribute to a, above, or to reducing the
severity of harassment takes only).
e. Avoid or minimize adverse effects
to marine mammal habitat (including
acoustic habitat), paying special
attention to the food base, activities that
block or limit passage to or from
biologically important areas, permanent
destruction of habitat, or temporary
destruction/disturbance of habitat
during a biologically important time.
f. For monitoring directly related to
mitigation—increase the probability of
detecting marine mammals, thus
allowing for more effective
implementation of the mitigation (shutdown zone, etc.).
Our final evaluation of measures that
meet one or more of the above goals
includes consideration of the following
factors in relation to one another: The
manner in which, and the degree to
which, the successful implementation of
the mitigation measures is expected to
reduce population-level impacts to
marine mammal species and stocks and
impacts to their habitat; the proven or
likely efficacy of the measures; and the
practicability of the suite of measures
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for applicant implementation, including
consideration of personnel safety,
practicality of implementation, and
impact on the effectiveness of the
military readiness activity.
NMFS reviewed the proposed
activities and the suite of proposed
mitigation measures as described in the
Navy’s LOA application to determine if
they would result in the least
practicable adverse effect on marine
mammals. NMFS worked with the Navy
in the development of the Navy’s
initially proposed measures, which are
informed by years of experience and
monitoring. Below are the mitigation
measures as agreed upon by the Navy
and NMFS. For additional details
regarding the Navy’s mitigation
measures, see Chapter 5 in the GOA
DSEIS/OEIS.
Lookouts
The Navy will have two types of
Lookouts for the purposes of conducting
visual observations: Those positioned
on ships; and those positioned ashore,
in aircraft, or on small boats. Lookouts
positioned on ships will diligently
observe the air and surface of the water.
They will have multiple observation
objectives, which include but are not
limited to detecting the presence of
biological resources and recreational or
fishing boats, observing the mitigation
zones, and monitoring for vessel and
personnel safety concerns.
Due to manning and space restrictions
on aircraft, small boats, and some Navy
ships, Lookouts for these platforms may
be supplemented by the aircraft crew or
pilot, boat crew, range site personnel, or
shore-side personnel. Lookouts
positioned in minimally manned
platforms may be responsible for tasks
in addition to observing the air or
surface of the water (e.g., navigation of
a helicopter or small boat). However, all
Lookouts will, considering personnel
safety, practicality of implementation,
and impact on the effectiveness of the
activity, comply with the observation
objectives described above for Lookouts
positioned on ships.
The procedural measures described in
the remainder of this section primarily
consist of having Lookouts during
specific training activities.
All personnel standing watch on the
bridge, Commanding Officers, Executive
Officers, maritime patrol aircraft
aircrews, anti-submarine warfare
helicopter crews, civilian equivalents,
and Lookouts will successfully
complete the United States Navy Marine
Species Awareness Training prior to
standing watch or serving as a Lookout.
Additional details on the Navy’s Marine
Species Awareness Training can be
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found in the GOA DSEIS/OEIS. The
Navy proposes to use one or more
Lookouts during the training activities
described below, which are organized
by stressor category.
Non-Impulsive Sound
Hull Mounted Mid-Frequency Active
Sonar
9979
other measures for these activities and
on these platforms when conducted in
the Study Area. The recommended
measure is provided below.
The Navy will have one Lookout on
ships conducting high-frequency or
non-hull mounted mid-frequency active
sonar activities associated with ASW
activities at sea.
The Navy’s current Lookout
mitigation measures during training
activities involving hull-mounted MFAS
include requirements such as the
number of personnel on watch and the
manner in which personnel are to
visually search the area in the vicinity
of the ongoing activity.
The Navy is proposing to maintain the
number of Lookouts currently
implemented for ships using hullmounted MFAS. Ships using hullmounted MFAS sources associated with
ASW activities at sea (with the
exception of ships less than 65 ft. [20 m]
in length, which are minimally manned)
will have two Lookouts at the forward
position. While using hull-mounted
MFAS sources underway, vessels less
than 65 ft. [20 m] in length and ships
that are minimally manned will have
one Lookout at the forward position due
to space and manning restrictions.
Explosives and Impulsive Sound
High-Frequency and Non-Hull-Mounted
Mid-Frequency Active Sonar
Currently, the Navy employs the
following Lookout procedures during
gunnery exercises:
• From the intended firing position,
trained Lookouts shall survey the
mitigation zone for marine mammals
prior to commencement and during the
exercise as long as practicable.
• If applicable, target towing vessels
shall maintain a Lookout. If a marine
mammal is sighted in the vicinity of the
exercise, the tow vessel shall
immediately notify the firing vessel in
order to secure gunnery firing until the
area is clear.
The Navy is proposing to continue
using the Lookout procedures currently
implemented for this activity. The Navy
will have one Lookout on the vessel or
aircraft conducting small-, medium-, or
large-caliber gunnery exercises against a
surface target. Towing vessels, if
applicable, shall also maintain one
Lookout.
The Navy currently conducts
activities using high-frequency and nonhull-mounted MFAS in the Study Area.
Non-hull-mounted MFAS training
activities include the use of aircraft
deployed sonobuoys, helicopter dipping
sonar, and submarine sonar. During
those activities, the Navy employs the
following mitigation measures regarding
Lookout procedures:
• Navy aircraft participating in
exercises at sea shall conduct and
maintain, when operationally feasible
and safe, surveillance for marine species
of concern as long as it does not violate
safety constraints or interfere with the
accomplishment of primary operational
duties.
• Helicopters shall observe/survey
the vicinity of an ASW training event
for 10 minutes before the first
deployment of active (dipping) sonar in
the water.
The Navy is proposing to continue
using the number of Lookouts (one)
currently implemented for aircraft
conducting non-hull-mounted MFA
sonar activities.
Mitigation measures do not currently
exist for other high-frequency active
sonar activities associated with ASW, or
for new platforms; therefore, the Navy is
proposing to add a new Lookout and
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Improved Extended Echo Ranging
Sonobuoys
The Navy is not proposing use of
Improved Extended Echo Ranging
Sonobuoys during the GOA TMAA
training activities.
Explosive Signal Underwater Sound
Buoys Using >0.5–2.5 Pound Net
Explosive Weight
Lookout measures do not currently
exist for explosive signal underwater
sound (SUS) buoy activities using >0.5–
2.5 pound (lb.) net explosive weight
(NEW). The Navy is proposing to add
this measure. Aircraft conducting SUS
activities using >0.5–2.5 lb. NEW will
have one Lookout.
Gunnery Exercises—Small-, Medium-,
and Large-Caliber Using a Surface
Target
Missile Exercises Using a Surface Target
Currently, the Navy employs the
following Lookout procedures during
missile exercises:
• Aircraft shall visually survey the
target area for marine mammals. Visual
inspection of the target area shall be
made by flying at 1,500 ft. (457 m) or
lower, if safe to do so, and at slowest
safe speed.
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• Firing or range clearance aircraft
must be able to actually see ordnance
impact areas.
The Navy is proposing to continue
using the Lookout procedures currently
implemented for this activity. When
aircraft are conducting missile exercises
against a surface target, the Navy will
have one Lookout positioned in an
aircraft.
Bombing Exercises (Explosive)
Currently, the Navy employs the
following Lookout procedures during
bombing exercises:
• If surface vessels are involved,
Lookouts shall survey for floating kelp
and marine mammals.
• Aircraft shall visually survey the
target and buffer zone for marine
mammals prior to and during the
exercise. The survey of the impact area
shall be made by flying at 1,500 ft.
(460 m) or lower, if safe to do so, and
at the slowest safe speed. Release of
ordnance through cloud cover is
prohibited: Aircraft must be able to
actually see ordnance impact areas.
Survey aircraft should employ most
effective search tactics and capabilities.
The Navy is proposing to (1) continue
implementing the current measures for
bombing exercises, and (2) clarify the
number of Lookouts currently
implemented for this activity. The Navy
will have one Lookout positioned in an
aircraft conducting bombing exercises,
and trained Lookouts in any surface
vessels involved.
Weapons Firing Noise During Gunnery
Exercises
The Navy is proposing to continue
using the number of Lookouts currently
implemented for gunnery exercises. The
Navy will have one Lookout on the ship
conducting explosive and non-explosive
gunnery exercises. This may be the
same Lookout described for Gunnery
Exercises—Small-, Medium-, and LargeCaliber Using a Surface Target when
that activity is conducted from a ship
against a surface target.
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Sinking Exercises
The Navy is proposing to continue
using the number of Lookouts currently
implemented for this activity. The Navy
will have two Lookouts (one positioned
in an aircraft and one on a vessel)
during sinking exercises.
Physical Disturbance and Strike
Vessels
Currently, the Navy employs the
following Lookout procedures to avoid
physical disturbance and strike of
marine mammals during at-sea training:
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• While underway, surface vessels
shall have at least two Lookouts with
binoculars; surfaced submarines shall
have at least one Lookout with
binoculars. Lookouts already posted for
safety of navigation and man-overboard
precautions may be used to fill this
requirement. As part of their regular
duties, Lookouts will watch for and
report to the Officer of the Deck the
presence of marine mammals.
Consistent with other ongoing Navy
Phase 2 training and testing (NWTT,
MITT, AFTT, HSTT), the Navy is
proposing to revise the mitigation
measures for this activity as follows:
While underway, vessels will have a
minimum of one Lookout.
Non-Explosive Practice Munitions
Gunnery Exercises—Small-, Medium-,
and Large-Caliber Using a Surface
Target
Currently, the Navy employs the same
mitigation measures for non-explosive
practice munitions—small-, medium-,
and large-caliber gunnery exercises—as
described above for Gunnery
Exercises—Small-, Medium-, and LargeCaliber Using a Surface Target.
The Navy is proposing to continue
using the number of Lookouts currently
implemented for these activities. The
Navy will have one Lookout during
activities involving non-explosive
practice munitions (e.g., small-,
medium-, and large-caliber gunnery
exercises) against a surface target.
Missile Exercises Using a Surface Target
Currently, the Navy employs the same
mitigation measures for non-explosive
missile exercises (including rockets)
using a surface target as described for
Missile Exercises Using a Surface Target
(explosive).
The Navy is proposing to continue
using the number of Lookouts currently
implemented for these activities. When
aircraft are conducting non-explosive
missile exercises (including exercises
using rockets) against a surface target,
the Navy will have one Lookout
positioned in an aircraft.
Bombing Exercises
Currently, the Navy employs the same
mitigation measures for non-explosive
bombing exercises as described for
Bombing Exercises (Explosive).
The Navy is proposing to continue
using the same Lookout procedures
currently implemented for these
activities. The Navy will have one
Lookout positioned in an aircraft during
non-explosive bombing exercises, and
trained Lookouts in any surface vessels
involved.
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Mitigation Zones
The Navy proposes to use mitigation
zones to reduce the potential impacts to
marine mammals from training
activities. Mitigation zones are
measured as the radius from a source.
Unique to each activity category, each
radius represents a distance that the
Navy will visually observe to help
reduce injury to marine species. Visual
detections of applicable marine species
will be communicated immediately to
the appropriate watch station for
information dissemination and
appropriate action. If the presence of
marine mammals is detected
acoustically, Lookouts posted in aircraft
and on surface vessels will increase the
vigilance of their visual surveillance. As
a reference, aerial surveys are typically
made by flying at 1,500 ft. (457 m)
altitude or lower at the slowest safe
speed.
Many of the proposed activities have
mitigation measures that are currently
being implemented, as required by
previous environmental documents or
consultations. Most of the current
mitigation zones for activities that
involve the use of impulsive and nonimpulsive sources were originally
designed to reduce the potential for
onset of TTS. For the GOA DSEIS/OEIS
and the LOA application, the Navy
updated the acoustic propagation
modeling to incorporate updated
hearing threshold metrics (i.e., upper
and lower frequency limits), updated
density data for marine mammals, and
factors such as an animal’s likely
presence at various depths. An
explanation of the acoustic propagation
modeling process can be found in the
Determination of Acoustic Effects on
Marine Mammals for the Gulf of Alaska
Training Supplemental Environmental
Impact Statement/Overseas
Environmental Impact Statement
technical report (Marine Species
Modeling Team, 2014).
As a result of the updates to the
acoustic propagation modeling, in some
cases the ranges to onset of TTS effects
are much larger than previous model
outputs. Due to the ineffectiveness and
unacceptable operational impacts
associated with mitigating these large
areas, the Navy is unable to mitigate for
onset of TTS for every activity. In this
GOA TMAA analysis, the Navy
developed each recommended
mitigation zone to avoid or reduce the
potential for onset PTS, out to the
predicted maximum range. In some
cases where the ranges to effects are
smaller than previous models estimated,
the mitigation zones were adjusted
accordingly to provide consistency
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Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Proposed Rules
across the measures. Mitigating to the
predicted maximum range to PTS
consequently also mitigates to the
predicted maximum range to onset
mortality (1 percent mortality), onset
slight lung injury, and onset slight
gastrointestinal tract injury, since the
maximum range to effects for these
criteria are shorter than for PTS.
Furthermore, in most cases, the
predicted maximum range to PTS also
consequently covers the predicted
average range to TTS. Table 8
summarizes the predicted average range
to TTS, average range to PTS, maximum
range to PTS, and recommended
mitigation zone for each activity
category, based on the Navy’s acoustic
propagation modeling results.
The activity-specific mitigation zones
are based on the longest range for all the
functional hearing groups. The
mitigation zone for a majority of
activities is driven by either the highfrequency cetaceans or the sea turtles
functional hearing groups. Therefore,
the mitigation zones are even more
protective for the remaining functional
hearing groups (i.e., low-frequency
cetaceans, mid-frequency cetaceans, and
pinnipeds), and likely cover a larger
portion of the potential range to onset of
TTS.
This evaluation includes explosive
ranges to TTS and the onset of auditory
injury, non-auditory injury, slight lung
injury, and mortality. For every source
proposed for use by the Navy, the
recommended mitigation zones
included in Table 8 exceed each of these
ranges. In some instances, the Navy
recommends mitigation zones that are
larger or smaller than the predicted
maximum range to PTS based on the
effectiveness and operational
assessments. The recommended
mitigation zones and their associated
assessments are provided throughout
the remainder of this section. The
recommended measures are either
currently implemented, are
modifications of current measures, or
are new measures.
For some activities specified
throughout the remainder of this
section, Lookouts may be required to
observe for concentrations of detached
floating vegetation (Sargassum or kelp
paddies), which are indicators of
potential marine mammal presence
within the mitigation zone. Those
specified activities will not commence if
floating vegetation (Sargassum or kelp
paddies) is observed within the
mitigation zone prior to the initial start
of the activity. If floating vegetation is
observed prior to the initial start of the
activity, the activity will be relocated to
an area where no floating vegetation is
observed. Training will not cease as a
result of indicators entering the
mitigation zone after activities have
commenced. This measure is intended
only for floating vegetation detached
from the seafloor.
TABLE 8—PREDICTED RANGES TO EFFECTS AND RECOMMENDED MITIGATION ZONES FOR EACH ACTIVITY CATEGORY
Activity category
Predicted (longest)
average range to
TTS
Representative
source (bin) 1
Predicted (longest)
average range to
PTS
Predicted maximum
range to PTS
Recommended
mitigation zone
Non-Impulse Sound
Hull-Mounted
Mid-Frequency Active
Sonar.
SQS–53 ASW hullmounted sonar
(MF1).
3,821 yd. (3.5 km) for
one ping.
100 yd. (91 m) for
one ping.
Not Applicable ..........
High-Frequency and
Non-Hull Mounted
Mid-Frequency Active
Sonar.
AQS–22 ASW dipping sonar (MF4).
230 yd. (210 m) for
one ping.
20 yd. (18 m) for one
ping.
Not applicable ...........
6 dB power down at
1,000 yd. (914 m);
4 dB power down
at 500 yd. (457 m);
and shutdown at
200 yd. (183 m).
200 yd. (183 m).
Explosive and Impulse Sound
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Signal Underwater
Sound (SUS) buoys
using > 0.5–2.5 lb.
NEW.
Gunnery Exercises—
Small- and MediumCaliber (Surface Target).
Gunnery Exercises—
Large-Caliber (Surface Target).
Missile Exercises (Including Rockets) up
to 250 lb. NEW Using
a Surface Target.
Missile Exercises up to
500 lb. NEW (Surface
Target).
Bombing Exercises .......
Sinking Exercises .........
Explosive sonobuoy
(E3).
290 yd. (265 m) ........
113 yd. (103 m) ........
309 yd. (283 m) ........
350 yd. (320 m).
40 mm projectile (E2)
190 yd. (174 m) ........
83 yd. (76 m) ............
182 yd. (167 m) ........
200 yd. (183 m).
5 in. projectiles (E5)
453 yd. (414 m) ........
186 yd. (170 m) ........
526 yd. (481 m) ........
600 yd. (549 m).
Maverick missile (E9)
949 yd. (868 m) ........
398 yd. (364 m) ........
699 yd. (639 m) ........
900 yd. (823 m).
Harpoon missile
(E10).
1,832 yd. (1.7 km) ....
731 yd. (668 m) ........
1,883 yd. (1.7 km) ....
2,000 yd. (1.8 km).
MK–84 2,000 lb.
bomb (E12).
Various up to MK–84
2,000 lb. bomb
(E12).
2,513 yd. (2.3 km) ....
991 yd. (906 m) ........
2,474 yd. (2.3 km) ....
2,500 yd. (2.3 km)2.
2,513 yd. (2.3 km) ....
991 yd. (906 m) ........
2,474 yd. (2.3 km) ....
2.5 nm (2).
1 This table does not provide an inclusive list of source bins; bins presented here represent the source bin with the largest range to effects
within the given activity category.
2 Recommended mitigation zones are larger than the modeled injury zones to account for multiple types of sources or charges being used.
Notes: in = inches, km = kilometers, lb. = pounds, m = meters, nm = nautical miles, PTS = Permanent Threshold Shift, TTS = Temporary
Threshold Shift, yd. = yards
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Non-Impulsive Sound
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Hull-Mounted Mid-Frequency Active
Sonar
The Navy is proposing to (1) continue
implementing the current measures for
MFAS and (2) to clarify the conditions
needed to recommence an activity after
a marine mammal has been detected.
Activities that involve the use of hullmounted MFA sonar will use Lookouts
for visual observation from a ship
immediately before and during the
activity. Mitigation zones for these
activities involve powering down the
sonar by 6 dB when a marine mammal
is sighted within 1,000 yd. (914 m) of
the sonar dome, and by an additional 4
dB when sighted within 500 yd. (457 m)
from the source, for a total reduction of
10 dB. Active transmissions will cease
if a marine mammal is sighted within
200 yd. (183 m). Active transmission
will recommence if any one of the
following conditions is met: (1) The
animal is observed exiting the
mitigation zone, (2) the animal is
thought to have exited the mitigation
zone based on its course and speed, (3)
the mitigation zone has been clear from
any additional sightings for a period of
30 minutes, (4) the ship has transited
more than 2,000 yd. (1.8 km) beyond the
location of the last sighting, or (5) the
ship concludes that dolphins are
deliberately closing in on the ship to
ride the ship’s bow wave (and there are
no other marine mammal sightings
within the mitigation zone). Active
transmission may resume when
dolphins are bow riding because they
are out of the main transmission axis of
the active sonar while in the shallowwave area of the ship bow.
High-Frequency and Non-Hull-Mounted
Mid-Frequency Active Sonar
Non-hull-mounted MFA sonar
training activities include the use of
aircraft deployed sonobuoys and
helicopter dipping sonar. The Navy is
proposing to: (1) Continue
implementing the current mitigation
measures for activities currently being
executed, such as dipping sonar
activities; (2) extend the implementation
of its current mitigation to all other
activities in this category; and (3) clarify
the conditions needed to recommence
an activity after a sighting. The
recommended measures are provided
below.
Mitigation will include visual
observation from a vessel or aircraft
(with the exception of platforms
operating at high altitudes) immediately
before and during active transmission
within a mitigation zone of 200 yd. (183
m) from the active sonar source. For
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activities involving helicopter deployed
dipping sonar, visual observation will
commence 10 minutes before the first
deployment of active dipping sonar.
Helicopter dipping and sonobuoy
deployment will not begin if
concentrations of floating vegetation
(kelp paddies), are observed in the
mitigation zone. If the source can be
turned off during the activity, active
transmission will cease if a marine
mammal is sighted within the
mitigation zone. Active transmission
will recommence if any one of the
following conditions is met: (1) The
animal is observed exiting the
mitigation zone, (2) the animal is
thought to have exited the mitigation
zone based on its course and speed, (3)
the mitigation zone has been clear from
any additional sightings for a period of
10 minutes for an aircraft-deployed
source, (4) the mitigation zone has been
clear from any additional sightings for a
period of 30 minutes for a vesseldeployed source, (5) the vessel or
aircraft has repositioned itself more than
400 yd. (370 m) away from the location
of the last sighting, or (6) the vessel
concludes that dolphins are deliberately
closing in to ride the vessel’s bow wave
(and there are no other marine mammal
sightings within the mitigation zone).
Explosives and Impulsive Sound
Explosive Signal Underwater Sound
Buoys Using >0.5–2.5 Pound Net
Explosive Weight
Mitigation measures do not currently
exist for activities using explosive signal
underwater sound (SUS) buoys.
The Navy is proposing to add the
following recommended measures.
Mitigation will include pre-exercise
aerial monitoring during deployment
within a mitigation zone of 350 yd. (320
m) around an explosive SUS buoy.
Explosive SUS buoys will not be
deployed if concentrations of floating
vegetation (kelp paddies) are observed
in the mitigation zone (around the
intended deployment location). SUS
deployment will cease if a marine
mammal is sighted within the
mitigation zone. Deployment will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on its course and
speed, or (3) the mitigation zone has
been clear from any additional sightings
for a period of 10 minutes.
Passive acoustic monitoring will also
be conducted with Navy assets, such as
sonobuoys, already participating in the
activity. These assets would only detect
vocalizing marine mammals within the
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frequency bands monitored by Navy
personnel. Passive acoustic detections
would not provide range or bearing to
detected animals, and therefore cannot
provide locations of these animals.
Passive acoustic detections would be
reported to Lookouts posted in aircraft
in order to increase vigilance of their
visual surveillance.
Gunnery Exercises—Small- and
Medium-Caliber Using a Surface Target
The Navy is proposing to (1) continue
implementing the current mitigation
measures for this activity, (2) clarify the
conditions needed to recommence an
activity after a sighting, and (3) add a
requirement to visually observe for kelp
paddies.
Mitigation will include visual
observation from a vessel or aircraft
immediately before and during the
exercise within a mitigation zone of 200
yd. (183 m) around the intended impact
location. Vessels will observe the
mitigation zone from the firing position.
When aircraft are firing, the aircrew will
maintain visual watch of the mitigation
zone during the activity. The exercise
will not commence if concentrations of
floating vegetation (kelp paddies) are
observed in the mitigation zone. Firing
will cease if a marine mammal is
sighted within the mitigation zone.
Firing will recommence if any one of
the following conditions is met: (1) The
animal is observed exiting the
mitigation zone, (2) the animal is
thought to have exited the mitigation
zone based on its course and speed, (3)
the mitigation zone has been clear from
any additional sightings for a period of
10 minutes for a firing aircraft, (4) the
mitigation zone has been clear from any
additional sightings for a period of 30
minutes for a firing ship, or (5) the
intended target location has been
repositioned more than 400 yd. (366 m)
away from the location of the last
sighting.
Gunnery Exercises—Large-Caliber
Explosive Rounds Using a Surface
Target
The Navy is proposing to (1) continue
using the currently implemented
mitigation zone measures for this
activity, (2) clarify the conditions
needed to recommence an activity after
a sighting, and (3) implement a
requirement to visually observe for kelp
paddies. The recommended measures
are provided below.
Mitigation will include visual
observation from a ship immediately
before and during the exercise within a
mitigation zone of 600 yd. (549 m)
around the intended impact location.
Ships will observe the mitigation zone
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from the firing position. The exercise
will not commence if concentrations of
floating vegetation (kelp paddies) are
observed in the mitigation zone. Firing
will cease if a marine mammal is
sighted within the mitigation zone.
Firing will recommence if any one of
the following conditions is met: (1) The
animal is observed exiting the
mitigation zone, (2) the animal is
thought to have exited the mitigation
zone based on its course and speed, or
(3) the mitigation zone has been clear
from any additional sightings for a
period of 30 minutes.
Missile Exercises Up to 250 Pound Net
Explosive Weight Using a Surface Target
Currently, the Navy employs a
mitigation zone of 1,800 yd. (1.6 km) for
all missile exercises. Because missiles
have a wide range of warhead strength,
the Navy is recommending two
mitigation zones; one for missiles with
warheads 250 lb. NEW and less, and a
larger mitigation zone for missiles with
larger warheads. The Navy is proposing
to (1) modify the mitigation measures
currently implemented for missile
exercises involving missiles with 250 lb.
NEW and smaller warheads by reducing
the mitigation zone from 1,800 yd. (1.6
km) to 900 yd. (823 m). This new,
reduced mitigation zone is a result of
the most recent acoustic propogation
modeling efforts (NAEMO) for the GOA
TMAA and is based on a range to effect
that is smaller than previously modeled
for missile exercises using a surface
target (as discussed below, the Navy is
proposing to increase the mitigation
zone for missiles with a NEW >250 lb.),
(2) clarify the conditions needed to
recommence an activity after a sighting,
and (3) adopt the marine mammal
mitigation zone size for floating
vegetation for ease of implementation.
The recommended measures are
provided below.
When aircraft are involved in the
missile firing, mitigation will include
visual observation by the aircrew or
supporting aircraft prior to
commencement of the activity within a
mitigation zone of 900 yd. (823 m)
around the deployed target. The
exercise will not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Firing will cease if a
marine mammal is sighted within the
mitigation zone. Firing will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on its course and
speed, or (3) the mitigation zone has
been clear from any additional sightings
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for a period of 10 minutes or 30 minutes
(depending on aircraft type).
Missile Exercises 251–500 Pound Net
Explosive Weight (Surface Target)
Current mitigation measures apply to
all missile exercises, regardless of the
warhead size. The Navy proposes to add
a mitigation zone that applies only to
missiles with a NEW of 251 to 500 lb.
The recommended measures are
provided below.
When aircraft are involved in the
missile firing, mitigation will include
visual observation by the aircrew prior
to commencement of the activity within
a mitigation zone of 2,000 yd. (1.8 km)
around the intended impact location.
The exercise will not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Firing will cease if a
marine mammal is sighted within the
mitigation zone. Firing will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on its course and
speed, or (3) the mitigation zone has
been clear from any additional sightings
for a period of 10 minutes or 30 minutes
(depending on aircraft type).
Bombing Exercises
Currently, the Navy employs the
following mitigation zone procedures
during bombing exercises:
• Ordnance shall not be targeted to
impact within 1,000 yd. (914 m) of
known or observed floating kelp or
marine mammals.
• A 1,000 yd. (914 m) radius
mitigation zone shall be established
around the intended target.
• The exercise will be conducted only
if marine mammals are not visible
within the mitigation zone.
The Navy is proposing to (1) maintain
the existing mitigation zone to be used
for non-explosive bombing activities, (2)
revise the mitigation zone procedures to
account for predicted ranges to impacts
to marine species when high explosive
bombs are used, (3) clarify the
conditions needed to recommence an
activity after a sighting, and (4) add a
requirement to visually observe for kelp
paddies.
Mitigation will include visual
observation from the aircraft
immediately before the exercise and
during target approach within a
mitigation zone of 2,500 yd. (2.3 km)
around the intended impact location for
explosive bombs and 1,000 yd. (920 m)
for non-explosive bombs. The exercise
will not commence if concentrations of
floating vegetation (kelp paddies) are
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observed in the mitigation zone.
Bombing will cease if a marine mammal
is sighted within the mitigation zone.
Bombing will recommence if any one of
the following conditions is met: (1) The
animal is observed exiting the
mitigation zone, (2) the animal is
thought to have exited the mitigation
zone based on its course and speed, or
(3) the mitigation zone has been clear
from any additional sightings for a
period of 10 minutes.
Sinking Exercises
The Navy is proposing to (1) modify
the mitigation measures currently
implemented for this activity by
increasing the mitigation zone from 2.0
nm to 2.5 nm, (2) clarify the conditions
needed to recommence an activity after
a sighting, (3) add a requirement to
visually observe for kelp paddies, and
(4) adopt the marine mammal and sea
turtle mitigation zone size for
concentrations of floating vegetation
and aggregations of jellyfish for ease of
implementation. The recommended
measures are provided below.
Mitigation will include visual
observation within a mitigation zone of
2.5 nm around the target ship hulk.
Sinking exercises will include aerial
observation beginning 90 minutes before
the first firing, visual observations from
vessels throughout the duration of the
exercise, and both aerial and vessel
observation immediately after any
planned or unplanned breaks in
weapons firing of longer than 2 hours.
Prior to conducting the exercise, the
Navy will review remotely sensed sea
surface temperature and sea surface
height maps to aid in deciding where to
release the target ship hulk.
The Navy will also monitor using
passive acoustics during the exercise.
Passive acoustic monitoring would be
conducted with Navy assets, such as
passive ships sonar systems or
sonobuoys, already participating in the
activity. These assets would only detect
vocalizing marine mammals within the
frequency bands monitored by Navy
personnel. Passive acoustic detections
would not provide range or bearing to
detected animals, and therefore cannot
provide locations of these animals.
Passive acoustic detections would be
reported to Lookouts posted in aircraft
and on vessels in order to increase
vigilance of their visual surveillance.
Lookouts will also increase observation
vigilance before the use of torpedoes or
unguided ordnance with a NEW of 500
lb. or greater, or if the Beaufort sea state
is a 4 or above.
The exercise will not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
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mitigation zone. The exercise will cease
if a marine mammal, sea turtle, or
aggregation of jellyfish is sighted within
the mitigation zone. The exercise will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on a
determination of its course and speed
and the relative motion between the
animal and the source, or (3) the
mitigation zone has been clear from any
additional sightings for a period of 30
minutes. Upon sinking the vessel, the
Navy will conduct post-exercise visual
surveillance of the mitigation zone for 2
hours (or until sunset, whichever comes
first).
Weapons Firing Noise During Gunnery
Exercises—Large-Caliber
The Navy currently has no mitigation
zone procedures for this activity in the
Study Area.
The Navy is proposing to adopt
measures currently used during Navy
gunnery exercises in other ranges
outside of the Study Area. For all
explosive and non-explosive largecaliber gunnery exercises conducted
from a ship, mitigation will include
visual observation immediately before
and during the exercise within a
mitigation zone of 70 yd. (46 m) within
30 degrees on either side of the gun
target line on the firing side. The
exercise will not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Firing will cease if a
marine mammal is sighted within the
mitigation zone. Firing will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on its course and
speed, (3) the mitigation zone has been
clear from any additional sightings for a
period of 30 minutes, or (4) the vessel
has repositioned itself more than 140
yd. (128 m) away from the location of
the last sighting.
Physical Disturbance and Strike
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Vessels
The Navy’s current measures to
mitigate potential impacts to marine
mammals from vessel and in-water
device strikes during training activities
are provided below:
• Naval vessels shall maneuver to
keep at least 500 yd. (457 m) away from
any observed whale in the vessel’s path
and avoid approaching whales head-on.
These requirements do not apply if a
vessel’s safety is threatened, such as
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when change of course will create an
imminent and serious threat to a person,
vessel, or aircraft, and to the extent
vessels are restricted in their ability to
maneuver. Restricted maneuverability
includes, but is not limited to, situations
when vessels are engaged in dredging,
submerged activities, launching and
recovering aircraft or landing craft,
minesweeping activities, replenishment
while underway and towing activities
that severely restrict a vessel’s ability to
deviate course.
• Vessels will take reasonable steps to
alert other vessels in the vicinity of the
whale. Given rapid swimming speeds
and maneuverability of many dolphin
species, naval vessels would maintain
normal course and speed on sighting
dolphins unless some condition
indicated a need for the vessel to
maneuver.
The Navy is proposing to continue to
use the 500 yd. (457 m) mitigation zone
currently established for whales, and to
implement a 200 yd. (183 m) mitigation
zone for all other marine mammals.
Vessels will avoid approaching marine
mammals head on and will maneuver to
maintain a mitigation zone of 500 yd.
(457 m) around observed whales and
200 yd. (183 m) around all other marine
mammals (except bow-riding dolphins),
providing it is safe to do so. The Navy
is clarifying its existing speed protocol;
while in transit, Navy vessels shall be
alert at all times, use extreme caution,
and proceed at a ‘‘safe speed’’ so that
the vessel can take proper and effective
action to avoid a collision with any
sighted object or disturbance, including
any marine mammal or sea turtle, and
can be stopped within a distance
appropriate to the prevailing
circumstances and conditions.
Towed In-Water Devices
The Navy currently has no mitigation
zone procedures for this activity in the
Study Area.
The Navy is proposing to adopt
measures currently used in other ranges
outside of the Study Area during
activities involving towed in-water
devices. The Navy will ensure that
towed in-water devices being towed
from manned platforms avoid coming
within a mitigation zone of 250 yd. (229
m) around any observed marine
mammal, providing it is safe to do so.
Non-Explosive Practice Munitions
Gunnery Exercises—Small-, Medium-,
and Large-Caliber Using a Surface
Target
Currently, the Navy employs the same
mitigation measures for non-explosive
gunnery exercises as described above for
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Gunnery Exercises—Small-, Medium-,
and Large-Caliber Using a Surface
Target.
The Navy is proposing to (1) continue
using the mitigation measures currently
implemented for this activity, and (2)
clarify the conditions needed to
recommence an activity after a sighting.
The recommended measures are
provided below.
Mitigation will include visual
observation from a vessel or aircraft
immediately before and during the
exercise within a mitigation zone of 200
yd. (183 m) around the intended impact
location. The exercise will not
commence if concentrations of floating
vegetation (kelp paddies) are observed
in the mitigation zone. Firing will cease
if a marine mammal is sighted within
the mitigation zone. Firing will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on its course and
speed, (3) the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes for a firing aircraft,
(4) the mitigation zone has been clear
from any additional sightings for a
period of 30 minutes for a firing ship,
or (5) the intended target location has
been repositioned more than 400 yd.
(366 m) away from the location of the
last sighting.
Bombing Exercises
The Navy is proposing to continue
using the mitigation measures currently
implemented for this activity. The
recommended measure includes
clarification of a post-sighting activity
recommencement criterion.
Mitigation will include visual
observation from the aircraft
immediately before the exercise and
during target approach within a
mitigation zone of 1,000 yd. (914 m)
around the intended impact location.
The exercise will not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Bombing will cease if
a marine mammal is sighted within the
mitigation zone. Bombing will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on its course and
speed, or (3) the mitigation zone has
been clear from any additional sightings
for a period of 10 minutes.
Missile Exercises (Including Rockets)
Using a Surface Target
The Navy is proposing to (1) modify
the mitigation measures currently
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implemented for this activity by
reducing the mitigation zone from 1,800
yd. (1.6 km) to 900 yd. (823 m), (2)
clarify the conditions needed to
recommence an activity after a sighting,
(3) adopt the marine mammal and sea
turtle mitigation zone size for floating
vegetation for ease of implementation,
and (4) modify the platform of
observation to eliminate the
requirement to observe when ships are
firing. The recommended measures are
provided below.
When aircraft are firing, mitigation
will include visual observation by the
aircrew or supporting aircraft prior to
commencement of the activity within a
mitigation zone of 900 yd. (823 m)
around the deployed target. The
exercise will not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Firing will cease if a
marine mammal is sighted within the
mitigation zone. Firing will
recommence if any one of the following
conditions is met: (1) The animal is
observed exiting the mitigation zone, (2)
the animal is thought to have exited the
mitigation zone based on a
determination of its course and speed
and the relative motion between the
animal and the source, or (3) the
mitigation zone has been clear from any
additional sightings for a period of 10
minutes or 30 minutes (depending on
aircraft type).
Consideration of Time/Area Limitations
The Navy’s and NMFS’ analysis of
effects to marine mammals considers
emergent science regarding locations
where cetaceans are known to engage in
specific activities (e.g., feeding,
breeding/calving, or migration) at
certain times of the year that are
important to individual animals as well
as populations of marine mammals (see
discussion in Van Parijs, 2015). Where
data were available, Van Parijs (2015)
identified areas that are important in
this way and named the areas
Biologically Important Areas (BIAs). It is
important to note that the BIAs were not
meant to define exclusionary zones, nor
were they meant to be locations that
serve as sanctuaries from human
activity, or areas analogous to marine
protected areas (see Ferguson et al.
(2015a) regarding the envisioned
purpose for the BIA designations). The
delineation of BIAs does not have direct
or immediate regulatory consequences,
although it is appropriate to consider
them as part of the body of science that
may inform mitigation decisions,
depending on the circumstances. The
intention was that the BIAs would serve
as resource management tools and that
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they be considered along with any new
information as well as, ‘‘existing density
estimates, range-wide distribution data,
information on population trends and
life history parameters, known threats to
the population, and other relevant
information’’ (Van Parijs, 2015).
The Navy and NMFS have supported
and will continue to support the
Cetacean and Sound Mapping project,
including representation on the
Cetacean Density and distribution
Working Group (CetMap), which
informed NMFS’ identification of BIAs.
The same marine mammal density data
present in the Navy’s Marine Species
Density Database Technical Report (U.S.
Department of the Navy, 2014) and used
in the analysis for the GOA SEIS/OEIS
was used in the development of BIAs.
The final products, including the Gulf of
Alaska BIAs, from this mapping effort
were completed and published in March
2015 (Aquatic Mammals, 2015;
Calambokidis et al., 2015; Ferguson et
al., 2015a, 2015b; Van Parijs, 2015). 131
BIAs for 24 marine mammal species,
stocks, or populations in seven regions
within U.S. waters were identified
(Ferguson et al., 2015a). BIAs have been
identified in the Gulf of Alaska in the
vicinity of the GOA TMAA Study Area
and include migratory and feeding BIAs
for gray whale and North Pacific right
whale, respectively. However, the
degree of overlap between these BIAs
and the Study area is negligible
geographically. NMFS’ recognition of an
area as biologically important for some
species activity is not equivalent to
designation of critical habitat under the
Endangered Species Act. Furthermore,
the BIAs identified by NMFS in and
around the Study Area do not represent
the totality of important habitat
throughout the marine mammals’ full
range.
NMFS’ Office of Protected Resources
routinely considers available
information about marine mammal
habitat use to inform discussions with
applicants regarding potential spatiotemporal limitations on their activities
that might help effect the least
practicable adverse impact on species or
stocks and their habitat. BIAs are useful
tools for planning and impact
assessments and are being provided to
the public via this Web site:
www.cetsound.noaa.gov. While these
BIAs are useful tools for analysts, any
decisions regarding protective measures
based on these areas must go through
the normal MMPA evaluation process
(or any other statutory process that the
BIAs are used to inform); the
identification of a BIA does not presuppose any specific management
decision associated with those areas,
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9985
nor does it have direct or immediate
regulatory consequences. NMFS and the
Navy have discussed the BIAs listed
above, what Navy activities take place
in these areas (in the context of what
their effects on marine mammals might
be or whether additional mitigation is
necessary), and what measures could be
implemented to reduce impacts in these
areas (in the context of their potential to
reduce marine mammal impacts and
their practicability). An assessment of
the potential spatio-temporal and
activity overlap of Navy training
activities with the Gulf of Alaska BIAs
listed above is included below and in
Chapter 3.8 of the GOA DSEIS/OEIS. In
addition, in the Group and SpeciesSpecific Analysis section of this
proposed rule NMFS has preliminarily
assessed the potential effects of Navy
training on the ability of gray whale and
North Pacific right whale to engage in
those activities for which the BIAs have
been identified (migratory and feeding).
As we learn more about marine mammal
density, distribution, and habitat use
(and the BIAs are updated), NMFS and
the Navy will continue to reevaluate
appropriate time-area measures through
the Adaptive Management process
outlined in these regulations.
North Pacific Right Whale Feeding
Area—The NMFS-identified feeding
area for North Pacific right whales (see
Ferguson et al., 2015b) overlaps slightly
with the GOA TMAA’s southwestern
corner. This feeding area is applicable
from June to September so there is
temporal overlap with the proposed
Navy training but there is minimal (<1
percent) spatial overlap between this
feeding area and the GOA TMAA (see
Figure 3.8–2 of the GOA DSEIS/OEIS).
Given their current extremely low
population numbers and the general
lack of sightings in the Gulf of Alaska,
the occurrence of right whales in the
GOA TMAA is considered rare. North
Pacific right whales have not been
visually detected in the GOA TMAA
since at least the 1960s. The Quinn
Seamount passive acoustic detections in
ˇ
´
summer 2013 (Sirovic et al., 2014) are
the only known potential occurrence
records of this species in the GOA
TMAA in recent years.
Grey Whale Migratory Area—The
NMFS-identified migration area for gray
whales, which was bounded by the
extent of the continental shelf (as
provided in Ferguson et al., 2015b), has
slight (<1 percent) overlap with the
GOA TMAA at its northernmost corner
and western edge (see Ferguson et al.,
2015b; See Figure 3.8–4 of the GOA
DSEIS/OEIS). However, this migration
area is applicable only between March
to May (Spring) and November to
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January (Fall) (see Aquatic Mammals,
2015). This NMFS-identified gray whale
migration area would not be applicable
during the months when training has
historically occurred (June/July) and is
not likely to have temporal overlap with
most of the proposed timeframe (May to
October; summer) for Navy training in
the GOA TMAA. It is worth mentioning
that the Navy’s acoustic analysis did not
predict any takes of gray whales in the
GOA TMAA and NMFS is not
authorizing any takes of this species (see
Group and Species-Specific Analysis
section later in this proposed rule).
Potential Training Overlap with
BIAs—It is very unlikely that Navy
training would occur in these nearshore
locations adjacent to the GOA TMAA
boundary where the overlap with BIAs
occurs. To ensure that the Navy is able
to conduct realistic training, Navy units
must maintain sufficient room to
maneuver. Therefore, training activities
will typically take place some distance
away from an operating area boundary
to ensure sufficient sea or air space is
available for tactical maneuvers within
an approved operating area such as the
GOA TMAA. The Navy also does not
typically train next to any limiting
boundary because it precludes tactical
consideration of the adjacent sea space
and airspace beyond the boundary from
being a potential threat axis during
activities such as anti-submarine
warfare training. It is also the case that
Navy training activities will generally
not be located where it is likely there
would be interference from civilian
vessels and aircraft that are not
participating in the training activity.
The nearshore boundary of the GOA
TMAA is the location for multiple
commercial vessel transit lanes, ship
traffic, and low-altitude air routes,
which all pass through the NMFSidentified feeding area and the
identified migration area (see Figure
3.8–9 of the GOA DSEIS/OEIS). This
level of civilian activity may otherwise
conflict with Navy training activities if
those Navy activities were located at
that margin of the GOA TMAA and as
a result such an area is generally
avoided.
In short, the corners of and edge of the
GOA TMAA are seldom if ever a
suitable location for sustained, realistic,
and coordinated training using sonar
and other active acoustic sources or
explosives. The Navy has lookouts and
mitigation measures in place to
maneuver away from and around
marine mammals, and Navy vessels and
aircraft are no more likely to cause any
impact to these species than any other
non-Navy vessels or aircraft in the area.
The Navy’s stand-off distance for vessels
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of 500 yd. (457 m) and mitigation
procedures (see Proposed Mitigation)
further reduce the potential that there
would be any biologically meaningful
effect to feeding or migration should
animals be present and detected during
a very unlikely Navy training event
using sonar and other active acoustic
sources or explosives in one of these
overlapping NMFS-identified areas.
Therefore, North Pacific right whales
and gray whales in the NMFS-identified
feeding or migration areas at these
boundaries of the GOA TMAA are very
unlikely to have their feeding or
migration activities affected by Navy
training activities using sonar and other
active acoustic sources.
Conclusion—Based on the likely
locations for training in the GOA
TMAA, the Navy and NMFS anticipate
that proposed training activities would
have very limited, if any, spatial or
temporal overlap with the designated
North Pacific right whale area or gray
whale biologically important areas.
Therefore, it is unlikely that Navy
training would have any biologically
meaningful effect on North Pacific right
whale feeding behavior or gray whale
migration behavior in these areas.
Moreover, appropriate mitigation
measures (as detailed in Proposed
Mitigation above) would be
implemented for any detected marine
mammals and thus further reduce the
potential for the feeding or migration
activities to be affected.
Stranding Response Plan
NMFS and the Navy developed a
Stranding Response Plan for GOA
TMAA in 2011 as part of the previous
(2011–2016) incidental take
authorization and rulemaking process
for the Study Area. The Stranding
Response Plan is specifically intended
to outline the applicable requirements
in the event that a marine mammal
stranding is reported in the complexes
during a major training exercise. NMFS
considers all plausible causes within the
course of a stranding investigation and
this plan in no way presumes that any
strandings are related to, or caused by,
Navy training activities, absent a
determination made during
investigation. The plan is designed to
address mitigation, monitoring, and
compliance. The current Stranding
Response Plan for the GOA TMAA is
available for review at: https://
www.nmfs.noaa.gov/pr/permits/goa_
tmaa_stranding_protocol.pdf. NMFS
and the Navy are currently updating the
Stranding Response Plan for the GOA
TMAA for 2016–2021 training activities.
The updated Stranding Response Plan
will be finalized prior to the release of
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the final rule, and will be made
available for review at: https://
www.nmfs.noaa.gov/pr/permits/
incidental/military.htm#navy_goa2021.
In addition, modifications to the
Stranding Response Plan may also be
made through the adaptive management
process.
Mitigation Conclusions
NMFS has carefully evaluated the
Navy’s proposed mitigation measures—
many of which were developed with
NMFS’ input during the first phase of
Navy Training authorizations—and
considered a broad range of other
measures in the context of ensuring that
NMFS prescribes the means of effecting
the least practicable adverse impact on
the affected marine mammal species
and stocks and their habitat. Our
evaluation of potential measures
included consideration of the following
factors in relation to one another: The
manner in which, and the degree to
which, the successful implementation of
the mitigation measures is expected to
reduce the likelihood and/or magnitude
of adverse impacts to marine mammal
species and stocks and their habitat; the
proven or likely efficacy of the
measures; and the practicability of the
suite of measures for applicant
implementation, including
consideration of personnel safety,
practicality of implementation, and
impact on the effectiveness of the
military readiness activity.
Based on our evaluation of the Navy’s
proposed measures, as well as other
measures considered by NMFS, NMFS
has determined preliminarily that the
Navy’s proposed mitigation measures
(especially when the adaptive
management component is taken into
consideration (see Adaptive
Management, below)) are adequate
means of effecting the least practicable
adverse impacts on marine mammals
species or stocks and their habitat,
paying particular attention to rookeries,
mating grounds, and areas of similar
significance, while also considering
personnel safety, practicality of
implementation, and impact on the
effectiveness of the military readiness
activity.
The proposed rule comment period
provides the public an opportunity to
submit recommendations, views, and/or
concerns regarding this action and the
proposed mitigation measures. While
NMFS has determined preliminarily
that the Navy’s proposed mitigation
measures would affect the least
practicable adverse impact on the
affected species or stocks and their
habitat, NMFS will consider all public
comments to help inform our final
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decision. Consequently, the proposed
mitigation measures may be refined,
modified, removed, or added to prior to
the issuance of the final rule based on
public comments received, and where
appropriate, further analysis of any
additional mitigation measures.
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Proposed Monitoring
Section 101(a)(5)(A) of the MMPA
states that in order to issue an ITA for
an activity, NMFS must set forth
‘‘requirements pertaining to the
monitoring and reporting of such
taking’’. The MMPA implementing
regulations at 50 CFR 216.104 (a)(13)
indicate that requests for LOAs must
include the suggested means of
accomplishing the necessary monitoring
and reporting that will result in
increased knowledge of the species and
of the level of taking or impacts on
populations of marine mammals that are
expected to be present.
Integrated Comprehensive Monitoring
Program (ICMP)
The Navy’s ICMP is intended to
coordinate monitoring efforts across all
regions and to allocate the most
appropriate level and type of effort for
each range complex based on a set of
standardized objectives, and in
acknowledgement of regional expertise
and resource availability. The ICMP is
designed to be a flexible, scalable, and
adaptable through the adaptive
management and strategic planning
processes to periodically assess progress
and reevaluate objectives. Although the
ICMP does not specify actual
monitoring field work or projects, it
does establish top-level goals that have
been developed in coordination with
NMFS. As the ICMP is implemented,
detailed and specific studies will be
developed which support the Navy’s
top-level monitoring goals. In essence,
the ICMP directs that monitoring
activities relating to the effects of Navy
training and testing activities on marine
species should be designed to contribute
towards one or more of the following
top-level goals:
• An increase in our understanding of
the likely occurrence of marine
mammals and/or ESA-listed marine
species in the vicinity of the action (i.e.,
presence, abundance, distribution, and/
or density of species);
• An increase in our understanding of
the nature, scope, or context of the
likely exposure of marine mammals
and/or ESA-listed species to any of the
potential stressor(s) associated with the
action (e.g., tonal and impulsive sound),
through better understanding of one or
more of the following: (1) The action
and the environment in which it occurs
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(e.g., sound source characterization,
propagation, and ambient noise levels);
(2) the affected species (e.g., life history
or dive patterns); (3) the likely cooccurrence of marine mammals and/or
ESA-listed marine species with the
action (in whole or part) associated with
specific adverse effects, and/or; (4) the
likely biological or behavioral context of
exposure to the stressor for the marine
mammal and/or ESA-listed marine
species (e.g., age class of exposed
animals or known pupping, calving or
feeding areas);
• An increase in our understanding of
how individual marine mammals or
ESA-listed marine species respond
(behaviorally or physiologically) to the
specific stressors associated with the
action (in specific contexts, where
possible, e.g., at what distance or
received level);
• An increase in our understanding of
how anticipated individual responses,
to individual stressors or anticipated
combinations of stressors, may impact
either: (1) The long-term fitness and
survival of an individual; or (2) the
population, species, or stock (e.g.,
through effects on annual rates of
recruitment or survival);
• An increase in our understanding of
the effectiveness of mitigation and
monitoring measures;
• A better understanding and record
of the manner in which the authorized
entity complies with the ITA and
Incidental Take Statement;
• An increase in the probability of
detecting marine mammals (through
improved technology or methods), both
specifically within the safety zone (thus
allowing for more effective
implementation of the mitigation) and
in general, to better achieve the above
goals; and
• A reduction in the adverse impact
of activities to the least practicable
level, as defined in the MMPA.
Monitoring would address the ICMP
top-level goals through a collection of
specific regional and ocean basin
studies based on scientific objectives.
Quantitative metrics of monitoring effort
(e.g., 20 days of aerial surveys) would
not be a specific requirement. The
adaptive management process and
reporting requirements would serve as
the basis for evaluating performance and
compliance, primarily considering the
quality of the work and results
produced, as well as peer review and
publications, and public dissemination
of information, reports, and data. Details
of the ICMP are available online (https://
www.navymarinespeciesmonitoring.
us/).
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Strategic Planning Process for Marine
Species Monitoring
The Navy also developed the Strategic
Planning Process for Marine Species
Monitoring, which establishes the
guidelines and processes necessary to
develop, evaluate, and fund individual
projects based on objective scientific
study questions. The process uses an
underlying framework designed around
top-level goals, a conceptual framework
incorporating a progression of
knowledge, and in consultation with a
Scientific Advisory Group and other
regional experts. The Strategic Planning
Process for Marine Species Monitoring
would be used to set intermediate
scientific objectives, identify potential
species of interest at a regional scale,
and evaluate and select specific
monitoring projects to fund or continue
supporting for a given fiscal year. This
process would also address relative
investments to different range
complexes based on goals across all
range complexes, and monitoring would
leverage multiple techniques for data
acquisition and analysis whenever
possible. The Strategic Planning Process
for Marine Species Monitoring is also
available online (https://www.
navymarinespeciesmonitoring.us/).
Past and Current Monitoring in the
Study Area
NMFS has received multiple years’
worth of annual exercise and
monitoring reports addressing active
sonar use and explosive detonations
within the GOA TMAA and other Navy
range complexes. The data and
information contained in these reports
have been considered in developing
mitigation and monitoring measures for
the proposed training activities within
the Study Area. The Navy’s annual
exercise and monitoring reports may be
viewed at: https://www.nmfs.noaa.gov/
pr/permits/incidental/military.htm and
https://
www.navymarinespeciesmonitoring.us.
NMFS has reviewed these reports and
summarized the results, as related to
marine mammal monitoring, below.
1. The Navy has shown significant
initiative in developing its marine
species monitoring program and made
considerable progress toward reaching
goals and objectives of the ICMP.
2. Observation data from
watchstanders aboard navy vessels is
generally useful to indicate the presence
or absence of marine mammals within
the mitigation zones (and sometimes
beyond) and to document the
implementation of mitigation measures,
but does not provide useful speciesspecific information or behavioral data.
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3. Data gathered by experienced
marine mammal observers can provide
very valuable information at a level of
detail not possible with watchstanders.
4. Though it is by no means
conclusive, it is worth noting that no
instances of obvious behavioral
disturbance have been observed by
Navy watchstanders or experienced
marine mammal observers conducting
visual monitoring.
5. Visual surveys generally provide
suitable data for addressing questions of
distribution and abundance of marine
mammals, but are much less effective at
providing information on movements
and behavior, with a few notable
exceptions where sightings are most
frequent.
6. Passive acoustics and animal
tagging have significant potential for
applications addressing animal
movements and behavioral response to
Navy training activities, but require a
longer time horizon and heavy
investment in analysis to produce
relevant results.
7. NMFS and the Navy should more
carefully consider what and how
information should be gathered by
watchstanders during training exercises
and monitoring events, as some reports
contain different information, making
cross-report comparisons difficult.
This section is a summary of Navyfunded compliance monitoring in the
GOA TMAA since 2011. Additional
Navy-funded monitoring outside of and
in addition to the Navy’s commitments
to NMFS is provided later in this
section.
Gulf of Alaska Study Area Monitoring,
2011–2015—During the LOA
development process for the 2011 GOA
FEIS/OEIS, the Navy and NMFS agreed
that monitoring in the Gulf of Alaska
should focus on augmenting existing
baseline data, since regional data on
species occurrence and density are
extremely limited. There have been four
reports to date covering work in the Gulf
of Alaska (U.S. Department of the Navy,
2011c, 2011d, 2012, 2013f). Collecting
baseline data was deemed a priority
prior to focusing on exercise monitoring
and behavioral response as is now being
done in other Navy OPAREAs and
ranges. There have been no previous
dedicated monitoring efforts during
Navy training activities in the GOA
TMAA with the exception of deployed
HARPs.
In July 2011, the Navy funded
deployment of two long-term bottommounted passive acoustic monitoring
buoys by Scripps Institute of
Oceanography. These HARPs were
deployed southeast of Kenai Peninsula
in the GOA TMAA with one on the shelf
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approximately 50 nm from land (in 111
fathoms [203 m] depth) and on the
shelf-break slope approximately 100 nm
from land (in 492 fathoms [900 m]
depth). Intended to be collected
annually, results from the first
deployment (July 2011–May 2012)
included over 5,756 hours of passive
acoustic data (Baumann-Pickering et al.
2012b). Identification of marine
mammal sounds included four baleen
whale species (blue whales, fin whales,
gray whales, and humpback whales) and
at least six species of odontocetes (killer
whale, sperm whale, Stejneger’s beaked
whale, Baird’s beaked whale, Cuvier’s
beaked whale, and an unidentified
porpoise presumed to be Dall’s
porpoise; Baumann-Pickering et al.,
2012b). Researchers also noted the
detection of anthropogenic sound from
commercial shipping. There were no
Navy activities or vessels in the area at
any time during the recording period.
Analysis of the passive acoustic
detections made from May 2012 to June
2013 were presented in BaumannPickering et al. (2013), Debich et al.
(2013), Debich et al. (2014), and the
Navy’s 2012, 2013, and 2014 GOA
TMAA annual monitoring report
submitted to NMFS (U.S. Department of
the Navy, 2012, 2013f, 2014d). Three
baleen whale species were detected:
Blue whales, fin whales, and humpback
whales. No North Pacific right whale
calls were detected at either site during
this monitoring period. At least seven
species of odontocetes were detected:
Risso’s dolphins, killer whales, sperm
whales, Baird’s beaked whales, Cuvier’s
beaked whales, Stejneger’s beaked
whales, and unidentified porpoises
(likely Dall’s porpoise). Focused
analysis of beaked whale echolocation
recordings were presented in BaumannPickering et al. (2013).
As also presented in Debich et al.
(2013) and U.S. Department of the Navy
(2013f), broadband ship noise was
found to be more common at the slope
and Pratt Seamount monitoring sites
within the GOA TMAA than at the
nearshore (on shelf) site. Sonar (a
variety of frequencies, most likely
fathometers and fish-finders), were more
common on the shelf and slope sites.
Very few explosions were recorded at
any of the three sites throughout the
monitoring period. Origin of the few
explosions detected are unknown, but
there was no Navy explosive use in the
GOA TMAA during this period, so these
explosive-like events may be related to
fisheries activity, lightning strikes, or
some other unidentified source. There
were no detections of Navy midfrequency sonar use in the recordings
(Debich et al. 2013, 2014; U.S.
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Department of the Navy 2013f, 2014d).
In September 2012, an additional HARP
buoy was deployed at Pratt Seamount
(near the east end of the GOA TMAA)
and in June 2013 two additional buoys
were deployed in the GOA TMAA: One
at the shelf-break near the southwest
corner of the GOA TMAA and one at
Quinn Seamount (the approximate
middle of the GOA TMAA’s southeast
boundary). This constitutes a total of
five Navy-funded concurrent long-term
passive acoustic monitoring packages
present in the GOA TMAA through fall
of 2014. Debich et al. (2013) reported
the first detection of a North Pacific
right whale at the Quinn Seamount site.
Over two days between June and August
2013, the Quinn seamount HARP
detected three hours of North Pacific
right whale calls (Debich et al., 2014,
ˇ
´
Sirovic et al., in press). Given the
recording device location near the
southwest border of the GOA TMAA,
inability of the device as configured to
determine call directionality, and likely
signal propagation of several 10s of
miles, it remains uncertain if the
detected calls orginated within or
outside of the GOA TMAA. Previous
related Navy funded monitoring at
multiple sites within the Study Area
reported no North Pacific right whale
detections (Baumann-Pickering et al.,
2012b, Debich et al., 2013). Additional
monitoring conducted in the GOA
TMAA through spring 2015 included
the deployment of five HARPs to detect
marine mammals and anthropogenic
sounds (Rice et al., 2015). Future
monitoring will include varying
numbers of HARPs or other passive
acoustic technologies based on annual
Adaptive Management discussions with
NMFS (see U.S. Department of the Navy
[2014d] for details in that regard).
In the Gulf of Alaska, the Navy has
also funded two previous marine
mammal surveys to gather occurrence
and density data. Although there was no
regulatory requirement for the Navy to
undertake either survey, the Navy
funded the data collection to first
support analysis of potential effects for
the 2011 GOA FEIS/OEIS and again
recently to support the current SEIS/
OEIS. The first Navy-funded survey
(GOALS) was conducted by NMFS in
April 2009 (see Rone et al., 2009). Linetransect survey visual data was gathered
to support distance sampling statistics
and acoustic data were collected over a
10-day period both within and outside
the GOA TMAA. This survey resulted in
sightings of several species and allowed
for the derivation of densities for fin and
humpback whale that supplemented
multiple previous survey efforts in the
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vicinity (Rone et al., 2009). In summer
2013, the Navy funded an additional
visual line-transect survey in the
offshore waters of the Gulf of Alaska
(Rone et al., 2014). The GOALS II
survey was a 30-day visual line-transect
survey supplemented by use of passive
acoustics and was a follow-on effort to
the previously Navy-funded GOALS
survey in 2009. The primary objectives
for the GOALS II survey were to acquire
baseline data to increase understanding
of the likely occurrence (i.e., presence,
abundance, distribution and/or density
of species) of beaked whales and ESAlisted marine mammals in the Gulf of
Alaska. Specific research objectives
were:
• Assess the abundance, spatial
distribution and/or density of marine
mammals, with a focus on beaked
whales and ESA-listed cetacean species
through visual line-transect surveys and
passive acoustics using a towed
hydrophone array and sonobuoys
• Increase knowledge of species’
vocal repertoire by linking visual
sightings to vocally active cetaceans, in
order to improve the effectiveness of
passive acoustic monitoring
• Attempt to photo-identify and
biopsy sample individual whales
opportunistically for analysis of
population structure, genetics and
habitat use
• Attempt to locate whales for
opportunistic satellite tagging using
visual and passive acoustic
methodology in order to provide
information on both large- and finescale movements and habitat use of
cetaceans
The Navy-funded GOALS II survey
also sampled four distinct habitat areas
(shelf, slope, offshore, and seamounts)
which were partitioned into four strata.
The survey design was intended to
provide uniform coverage within the
Gulf of Alaska. However, given the
overall limited knowledge of beaked
whales within the Gulf of Alaska, the
survey was also designed to provide
coverage of potential beaked whale
habitat and resulted in 13 encounters
with beaked whales numbering 67
individual animals (Rone et al., 2014).
The following additional details are
summarized from the presentation in
Rone et al. (2014). The visual survey
consisted of 4,504 km (2,431 nm) of
‘full-effort’ and included 349 km (188
nm) of ‘transit-effort.’ There was an
additional 375 km (202 nm) of ‘fogeffort’ (transect and transit). Based on
total effort, there were 802 sightings
(1,998 individuals) identified to species,
with an additional 162 sightings (228
individuals) of unidentified cetaceans
and pinnipeds. Acoustic surveying was
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conducted round-the-clock with a
towed-hydrophone array for 6,304 km
(3,997 nm) of line-transect effort totaling
426 hours of ‘standard’ monitoring, with
an additional 374 km (202 nm) of ∼30
hours of ‘non-standard’ and ‘chase’
effort. There were 379 acoustic
detections and 267 localizations of 6
identified cetacean species.
Additionally, 186 acoustic sonobuoys
were deployed with 7 identified
cetacean species detected. Two satellite
transmitter tags were deployed; a tag on
a blue whale (B. musculus) transmitted
for 9 days and a tag on a Baird’s beaked
whale (Berardius bairdii) transmitted for
15 days. Based on photo-identification
matches, the tagged blue whale had
been previously identified off Baja
California, Mexico, in 2005.
Photographs of five cetacean species
were collected for photo-identification
purposes: fin, humpback, blue, killer
(Orcinus orca) and Baird’s beaked
whales. The estimates of abundance and
density for five species were obtained
for the first time for the central Gulf of
Alaska. Overall, the Navy funded
GOALS II survey provided one of the
most comprehensive datasets on marine
mammal occurrence, abundance, and
distribution within that rarely surveyed
area (Rone et al., 2014).
NMFS has acknowledged that the
Navy’s GOA TMAA monitoring will
enhance understanding of marine
mammal vocalizations and distributions
within the offshore waters of the Gulf of
Alaska. Additionally, NMFS pointed out
that information gained from the
investigations associated with the
Navy’s monitoring may be used in the
adaptive management of monitoring
measures in subsequent NMFS
authorizations, if appropriate and in
consultation with NMFS. The Navy is
committed to structuring the Navysponsored research and monitoring
program to address both NMFS’
regulatory requirements as part of any
MMPA authorizations while at the same
time making significant contributions to
the greater body of marine mammal
science (see U.S. Department of the
Navy, 2013f).
Pacific Northwest Cetacean Tagging—
A Navy-funded effort in the Pacific
Northwest is ongoing and involves
attaching long-term satellite tracking
tags to migrating gray whales off the
coast of Oregon and northern California
(U.S. Department of the Navy, 2013e).
This study is being conducted by the
University of Oregon and has also
included tagging of other large whale
species such as humpback whales, fin
whales, and killer whales when
encountered. This effort is not
programmed, affiliated, or managed as
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part of the GOA TMAA monitoring, and
is a separate regional project, but has
provided information on marine
mammals and their movements that has
application to the Gulf of Alaska.
In one effort between May 2010 and
May 2013, satellite tracking tags were
placed on three gray whales, 11 fin
whales, five humpback whales, and two
killer whales off the Washington coast
(Schorr et al., 2013). One tag on an
Eastern North Pacific Offshore stock
killer whale, in a pod encountered off
Washington at Grays Harbor Canyon,
remained attached and continued to
transmit for approximately 3 months. In
this period, the animal transited a
distance of approximately 4,700 nm,
which included time spent in the
nearshore margins of the TMAA in the
Gulf of Alaska where it would be
considered part of the Offshore stock
(for stock designations, see Muto and
Angliss, 2015). In a second effort
between 2012 and 2013, tags were
attached to 11 Pacific Coast Feeding
Group gray whales near Crescent City,
California; in general, the tag-reported
positions indicated these whales were
moving southward at this time of year
(Mate, 2013). The Navy’s 2013 annual
monitoring report for the Northwest
Training and Testing Range contains the
details of the findings from both
research efforts described above (U.S.
Department of the Navy, 2013e).
Proposed Monitoring for the GOA
TMAA Study Area
Based on NMFS-Navy meetings in
June and October 2011, and the
upcoming annual monitoring meeting
scheduled for March 2016, future Navy
compliance monitoring, including
ongoing monitoring, will address ICMP
top-level goals through a series of
regional and ocean basin study
questions with a prioritization and
funding focus on species of interest as
identified for each range complex. The
ICMP will also address relative
investments to different range
complexes based on goals across all
range complexes, and monitoring will
leverage multiple techniques for data
acquisition and analysis whenever
possible.
Within the GOA TMAA Study Area,
the Navy’s monitoring for GOA TMAA
under this LOA authorization and
concurrently in other areas of the Pacific
Ocean will therefore be structured to
address region-specific species-specific
study questions in consultation with
NMFS.
The outcome of the March 2016 NavyNMFS monitoring meeting, including
any proposed monitoring during the
period covered by this proposed rule
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(2016–2021) will be discussed in the
final rule. In addition, Navy monitoring
projects proposed during the 2016–2021
GOA TMAA rulemaking period will be
posted on the Navy’s marine species
monitoring Web site (https://
www.navymarinespeciesmonitoring.us/
regions/pacific/current-projects/).
Ongoing Navy Research
The U.S. Navy is one of the world’s
leading organizations in assessing the
effects of human activities on the
marine environment including marine
mammals. From 2004 through 2013, the
Navy has funded over $240M
specifically for marine mammal
research. Navy scientists work
cooperatively with other government
researchers and scientists, universities,
industry, and non-governmental
conservation organizations in collecting,
evaluating, and modeling information
on marine resources. They also develop
approaches to ensure that these
resources are minimally impacted by
existing and future Navy operations. It
is imperative that the Navy’s R&D efforts
related to marine mammals are
conducted in an open, transparent
manner with validated study needs and
requirements. The goal of the Navy’s
R&D program is to enable collection and
publication of scientifically valid
research as well as development of
techniques and tools for Navy,
academic, and commercial use.
Historically, R&D programs are funded
and developed by the Navy’s Chief of
Naval Operations Energy and
Environmental Readiness Division
(OPNAV N45) and Office of Naval
Research (ONR), Code 322 Marine
Mammals and Biological Oceanography
Program. The primary focus of these
programs since the 1990s is on
understanding the effects of sound on
marine mammals, including
physiological, behavioral, and
ecological effects.
ONR’s current Marine Mammals and
Biology Program thrusts include, but are
not limited to: (1) monitoring and
detection research, (2) integrated
ecosystem research including sensor
and tag development, (3) effects of
sound on marine life (such as hearing,
behavioral response studies, physiology
[diving and stress], and PCAD), and (4)
models and databases for environmental
compliance.
To manage some of the Navy’s marine
mammal research programmatic
elements, OPNAV N45 developed in
2011 a new Living Marine Resources
(LMR) Research and Development
Program (https://www.lmr.navy.mil/).
The goal of the LMR Research and
Development Program is to identify and
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fill knowledge gaps and to demonstrate,
validate, and integrate new processes
and technologies to minimize potential
effects to marine mammals and other
marine resources. Key elements of the
LMR program include:
• Providing science-based
information to support Navy
environmental effects assessments for
research, development, acquisition,
testing and evaluation as well as Fleet
at-sea training, exercises, maintenance
and support activities.
• Improving knowledge of the status
and trends of marine species of concern
and the ecosystems of which they are a
part.
• Developing the scientific basis for
the criteria and thresholds to measure
the effects of Navy generated sound.
• Improving understanding of
underwater sound and sound field
characterization unique to assessing the
biological consequences resulting from
underwater sound (as opposed to
tactical applications of underwater
sound or propagation loss modeling for
military communications or tactical
applications).
• Developing technologies and
methods to monitor and, where
possible, mitigate biologically
significant consequences to living
marine resources resulting from naval
activities, emphasizing those
consequences that are most likely to be
biologically significant.
technology to improve environmental
performance, reduce costs, and enhance
and sustain mission capabilities. The
Programs respond to environmental
technology requirements that are
common to all of the military Services,
complementing the Services’ research
programs. SERDP and ESTCP promote
partnerships and collaboration among
academia, industry, the military
Services, and other Federal agencies.
They are independent programs
managed from a joint office to
coordinate the full spectrum of efforts,
from basic and applied research to field
demonstration and validation.
Adaptive Management
The final regulations governing the
take of marine mammals incidental to
Navy training activities in the Study
Area would contain an adaptive
management component carried over
from previous authorizations. Although
better than 5 years ago, our
understanding of the effects of Navy
training and testing activities (e.g.,
MFAS/HFAS, underwater detonations)
on marine mammals is still relatively
limited, and yet the science in this field
is evolving fairly quickly. These
circumstances make the inclusion of an
adaptive management component both
valuable and necessary within the
context of 5-year regulations for
activities that have been associated with
marine mammal mortality in certain
circumstances and locations.
Navy Research and Development
The reporting requirements associated
Navy Funded—Both the LMR and
with this proposed rule are designed to
provide NMFS with monitoring data
ONR Research and Development
from the previous year to allow NMFS
Programs periodically fund projects
to consider whether any changes are
within the Study Area. Some data and
appropriate. NMFS and the Navy would
results, when available from these R&D
meet to discuss the monitoring reports,
projects, are typically summarized in
Navy R&D developments, and current
the Navy’s annual range complex
science and whether mitigation or
Monitoring Reports that are currently
monitoring modifications are
submitted to the NMFS each year. In
appropriate. The use of adaptive
addition, the Navy’s Range Complex
management allows NMFS to consider
monitoring during training and testing
new information from different sources
activities is coordinated with the R&D
monitoring in a given region to leverage to determine (with input from the Navy
regarding practicability) on an annual or
research objectives, assets, and studies
biennial basis if mitigation or
where possible under the ICMP.
monitoring measures should be
The integration between the Navy’s
modified (including additions or
new LMR Research and Development
deletions). Mitigation measures could be
Program and related range complex
modified if new data suggests that such
monitoring will continue and improve
during this LOA application period with modifications would have a reasonable
likelihood of reducing adverse effects to
applicable results presented in GOA
marine mammals and if the measures
TMAA annual monitoring reports.
Other National Department of Defense are practicable.
The following are some of the
Funded Initiatives—Strategic
possible sources of applicable data to be
Environmental Research and
considered through the adaptive
Development Program (SERDP) and
management process: (1) Results from
Environmental Security Technology
monitoring and exercises reports, as
Certification Program (ESTCP) are the
DoD’s environmental research programs, required by MMPA authorizations; (2)
compiled results of Navy funded R&D
harnessing the latest science and
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studies; (3) results from specific
stranding investigations; (4) results from
general marine mammal and sound
research; and (5) any information which
reveals that marine mammals may have
been taken in a manner, extent, or
number not authorized by these
regulations or subsequent LOA.
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Proposed Reporting
In order to issue an ITA for an
activity, section 101(a)(5)(A) of the
MMPA states that NMFS must set forth
‘‘requirements pertaining to the
monitoring and reporting of such
taking’’. Effective reporting is critical
both to compliance as well as ensuring
that the most value is obtained from the
required monitoring. Some of the
reporting requirements are still in
development and the final rulemaking
may contain additional details not
contained here. Additionally, proposed
reporting requirements may be
modified, removed, or added based on
information or comments received
during the public comment period.
Reports from individual monitoring
events, results of analyses, publications,
and periodic progress reports for
specific monitoring projects would be
posted to the Navy’s Marine Species
Monitoring web portal: https://
www.navymarinespeciesmonitoring.us.
Currently, there are several different
reporting requirements pursuant to
these proposed regulations:
General Notification of Injured or Dead
Marine Mammals
Navy personnel would ensure that
NMFS (the appropriate Regional
Stranding Coordinator) is notified
immediately (or as soon as clearance
procedures allow) if an injured or dead
marine mammal is found during or
shortly after, and in the vicinity of, any
Navy training exercise utilizing MFAS,
HFAS, or underwater explosive
detonations. The Navy would provide
NMFS with species identification or a
description of the animal(s), the
condition of the animal(s) (including
carcass condition if the animal is dead),
location, time of first discovery,
observed behaviors (if alive), and
photographs or video (if available). The
Navy shall consult the Stranding
Response Plan to obtain more specific
reporting requirements for specific
circumstances.
Vessel Strike
NMFS has developed the following
language to address monitoring and
reporting measures specific to vessel
strike. Most of this language comes
directly from the Stranding Response
Plan for other Navy training and testing
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rulemakings. This section has also been
included in the regulatory text at the
end of this proposed rule. Vessel strike
during Navy training activities in the
Study Area is not anticipated; however,
in the event that a Navy vessel strikes
a whale, the Navy shall do the
following:
Immediately report to NMFS
(pursuant to the established
Communication Protocol) the:
• Species identification (if known);
• Location (latitude/longitude) of the
animal (or location of the strike if the
animal has disappeared);
• Whether the animal is alive or dead
(or unknown); and
• The time of the strike.
As soon as feasible, the Navy shall
report to or provide to NMFS, the:
• Size, length, and description
(critical if species is not known) of
animal;
• An estimate of the injury status
(e.g., dead, injured but alive, injured
and moving, blood or tissue observed in
the water, status unknown, disappeared,
etc.);
• Description of the behavior of the
whale during event, immediately after
the strike, and following the strike (until
the report is made or the animal is no
longer sighted);
• Vessel class/type and operational
status;
• Vessel length;
• Vessel speed and heading; and
• To the best extent possible, obtain
a photo or video of the struck animal,
if the animal is still in view.
Within 2 weeks of the strike, provide
NMFS:
• A detailed description of the
specific actions of the vessel in the 30minute timeframe immediately
preceding the strike, during the event,
and immediately after the strike (e.g.,
the speed and changes in speed, the
direction and changes in direction,
other maneuvers, sonar use, etc., if not
classified);
• A narrative description of marine
mammal sightings during the event and
immediately after, and any information
as to sightings prior to the strike, if
available; and use established Navy
shipboard procedures to make a camera
available to attempt to capture
photographs following a ship strike.
NMFS and the Navy will coordinate
to determine the services the Navy may
provide to assist NMFS with the
investigation of the strike. The response
and support activities to be provided by
the Navy are dependent on resource
availability, must be consistent with
military security, and must be
logistically feasible without
compromising Navy personnel safety.
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Assistance requested and provided may
vary based on distance of strike from
shore, the nature of the vessel that hit
the whale, available nearby Navy
resources, operational and installation
commitments, or other factors.
Annual GOA TMAA Monitoring Report
The Navy shall submit an annual
report of the GOA TMAA monitoring
describing the implementation and
results from the previous calendar year.
Data collection methods will be
standardized across range complexes
and study areas to allow for comparison
in different geographic locations.
Although additional information will be
gathered, Navy Lookouts collecting
marine mammal data pursuant to the
GOA TMAA monitoring plan shall, at a
minimum, provide the same marine
mammal observation data required in
§ 218.155. The report shall be submitted
either 90 days after the calendar year, or
90 days after the conclusion of the
monitoring year to be determined by the
Adaptive Management process. The
GOA TMAA Monitoring Report may be
provided to NMFS within a larger report
that includes the required Monitoring
Plan reports from multiple range
complexes and study areas (the multiRange Complex Annual Monitoring
Report). Such a report would describe
progress of knowledge made with
respect to monitoring plan study
questions across all Navy ranges
associated with the Integrated
Comprehensive Monitoring Program.
Similar study questions shall be treated
together so that progress on each topic
shall be summarized across all Navy
ranges. The report need not include
analyses and content that does not
provide direct assessment of cumulative
progress on the monitoring plan study
questions.
Annual GOA TMAA Exercise Report
Each year, the Navy shall submit a
preliminary report detailing the status of
authorized sound sources within 21
days after the anniversary of the date of
issuance of the LOA. Each year, the
Navy shall submit a detailed report
within 3 months after the anniversary of
the date of issuance of the LOA. The
annual report shall contain information
on Major Training Exercises (MTEs),
Sinking Exercise (SINKEX) events, and
a summary of all sound sources used
(total hours or quantity [per the LOA] of
each bin of sonar or other nonimpulsive source; total annual number
of each type of explosive exercises; and
total annual expended/detonated
rounds [missiles, bombs, sonobuoys,
etc.] for each explosive bin). The
analysis in the detailed report will be
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based on the accumulation of data from
the current year’s report and data
collected from previous the report.
Information included in the classified
annual reports may be used to inform
future adaptive management of
activities within the GOA TMAA.
Sonar Exercise Notification
The Navy shall submit to NMFS
(specific contact information to be
provided in LOA) an electronic report
within fifteen calendar days after the
completion of any major training
exercise indicating: Location of the
exercise; beginning and end dates of the
exercise; and type of exercise.
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5-Year Close-Out Exercise Report
This report will be included as part of
the 2021 annual exercise report. This
report will provide the annual totals for
each sound source bin with a
comparison to the annual allowance and
the 5-year total for each sound source
bin with a comparison to the 5-year
allowance. Additionally, if there were
any changes to the sound source
allowance, this report will include a
discussion of why the change was made
and include the analysis to support how
the change did or did not result in a
change in the SEIS and final rule
determinations. The report will be
submitted 3 months after the expiration
of the rule. NMFS will submit
comments on the draft close-out report,
if any, within 3 months of receipt. The
report will be considered final after the
Navy has addressed NMFS’ comments,
or 3 months after the submittal of the
draft if NMFS does not provide
comments.
Estimated Take of Marine Mammals
In the Potential Effects section,
NMFS’ analysis identified the lethal
responses, physical trauma, sensory
impairment (PTS, TTS, and acoustic
masking), physiological responses
(particular stress responses), and
behavioral responses that could
potentially result from exposure to
MFAS/HFAS or underwater explosive
detonations. In this section, the
potential effects to marine mammals
from MFAS/HFAS and underwater
detonation of explosives will be related
to the MMPA regulatory definitions of
Level A and Level B harassment and we
will attempt to quantify the effects that
might occur from the proposed training
activities in the Study Area.
As mentioned previously, behavioral
responses are context-dependent,
complex, and influenced to varying
degrees by a number of factors other
than just received level. For example, an
animal may respond differently to a
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sound emanating from a ship that is
moving towards the animal than it
would to an identical received level
coming from a vessel that is moving
away, or to a ship traveling at a different
speed or at a different distance from the
animal. At greater distances, the nature
of vessel movements could also
potentially not have any effect on the
animal’s response to the sound. In any
case, a full description of the suite of
factors that elicited a behavioral
response would require a mention of the
vicinity, speed and movement of the
vessel, or other factors. So, while sound
sources and the received levels are the
primary focus of the analysis and those
that are laid out quantitatively in the
regulatory text, it is with the
understanding that other factors related
to the training sometimes contribute to
the behavioral responses of marine
mammals, although they cannot be
quantified.
Definition of Harassment
As mentioned previously, with
respect to military readiness activities,
section 3(18)(B) of the MMPA defines
‘‘harassment’’ as: ‘‘(i) any act that
injures or has the significant potential to
injure a marine mammal or marine
mammal stock in the wild [Level A
Harassment]; or (ii) any act that disturbs
or is likely to disturb a marine mammal
or marine mammal stock in the wild by
causing disruption of natural behavioral
patterns, including, but not limited to,
migration, surfacing, nursing, breeding,
feeding, or sheltering, to a point where
such behavioral patterns are abandoned
or significantly altered [Level B
Harassment].’’ It is important to note
that, as Level B harassment is
interpreted here and quantified by the
behavioral thresholds described below,
the fact that a single behavioral pattern
(of unspecified duration) is abandoned
or significantly altered and classified as
a Level B take does not mean,
necessarily, that the fitness of the
harassed individual is affected either at
all or significantly, or that, for example,
a preferred habitat area is abandoned.
Further analysis of context and duration
of likely exposures and effects is
necessary to determine the impacts of
the estimated effects on individuals and
how those may translate to population
level impacts, and is included in the
Analysis and Negligible Impact
Determination.
Level B Harassment
Of the potential effects that were
described earlier in this proposed rule,
the following are the types of effects that
fall into the Level B harassment
category:
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Behavioral Harassment—Behavioral
disturbance that rises to the level
described in the definition above, when
resulting from exposures to nonimpulsive or impulsive sound, is
considered Level B harassment. Some of
the lower level physiological stress
responses discussed earlier would also
likely co-occur with the predicted
harassments, although these responses
are more difficult to detect and fewer
data exist relating these responses to
specific received levels of sound. When
Level B harassment is predicted based
on estimated behavioral responses,
those takes may have a stress-related
physiological component as well.
Except for some vocalization changes
that may be compensating for auditory
masking, all behavioral reactions are
assumed to occur due to a preceding
stress or cueing response; however,
stress responses cannot be predicted
directly due to a lack of scientific data.
Responses can overlap; for example, an
increased respiration rate is likely to be
coupled to a flight response or other
avoidance behavior. Factors to consider
when trying to predict a stress response
include the mammal’s life history stage
¨
and whether they are naıve or
experienced with the sound. Prior
experience with a stressor may be of
particular importance as repeated
experience with a stressor may dull the
stress response via acclimation (St.
Aubin and Dierauf, 2001; Bejder et al.,
2009).
As the statutory definition is currently
applied, a wide range of behavioral
reactions may qualify as Level B
harassment under the MMPA, including
but not limited to avoidance of the
sound source, temporary changes in
vocalizations or dive patters, temporary
avoidance of an area, or temporary
disruption of feeding, migrating, or
reproductive behaviors. The estimates
calculated by the Navy using the
acoustic thresholds do not differentiate
between the different types of potential
behavioral reactions. Nor do the
estimates provide information regarding
the potential fitness or other biological
consequences of the reactions on the
affected individuals. We therefore
consider the available scientific
evidence to determine the likely nature
of the modeled behavioral responses
and the potential fitness consequences
for affected individuals.
Acoustic Masking and
Communication Impairment—Acoustic
masking and communication
impairment are considered Level B
harassment as they can disrupt natural
behavioral patterns by interrupting or
limiting the marine mammal’s receipt or
transmittal of important information or
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environmental cues. As discussed in the
Analysis and Negligible Impact
Determination later in this proposed
rule, masking effects from MFAS/HFAS
are expected to be minimal. If masking
or communication impairment were to
occur briefly, it would be in the
frequency range of MFAS, which
overlaps with some marine mammal
vocalizations; however, it would likely
not mask the entirety of any particular
vocalization, communication series, or
other critical auditory cue, because the
signal length, frequency, and duty cycle
of the MFAS/HFAS signal does not
perfectly mimic the characteristics of
any marine mammal’s vocalizations.
The other sources used in Navy training,
many of either higher frequencies
(meaning that the sounds generated
attenuate even closer to the source) or
lower amounts of operation, are
similarly not expected to result in
masking or communication impairment.
Temporary Threshold Shift (TTS)—As
discussed previously, TTS can affect
how an animal behaves in response to
the environment, including
conspecifics, predators, and prey. The
following physiological mechanisms are
thought to play a role in inducing
auditory fatigue: Effects to sensory hair
cells in the inner ear that reduce their
sensitivity, modification of the chemical
environment within the sensory cells;
residual muscular activity in the middle
ear, displacement of certain inner ear
membranes; increased blood flow; and
post-stimulatory reduction in both
efferent and sensory neural output.
Ward (1997) suggested that when these
effects result in TTS rather than PTS,
they are within the normal bounds of
physiological variability and tolerance
and do not represent a physical injury.
Additionally, Southall et al. (2007)
indicate that although PTS is a tissue
injury, TTS is not because the reduced
hearing sensitivity following exposure
to intense sound results primarily from
fatigue, not loss, of cochlear hair cells
and supporting structures and is
reversible. Accordingly, NMFS classifies
TTS (when resulting from exposure to
sonar and other active acoustic sources
and explosives and other impulsive
sources) as Level B harassment, not
Level A harassment (injury).
The sound characteristics that
correlate with specific stress responses
in marine mammals are poorly
understood. Therefore, in practice, a
stress response is assumed if a
physiological reaction such as a hearing
loss (threshold shift—i.e., TTS or PTS)
or trauma is predicted (or if a behavioral
response is predicted, as discussed in
the Level B Harassment section).
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Only non-TTS behavioral reactions
and TTS are anticipated with the GOA
TMAA training activities, and these
Level B behavioral harassment takes are
enumerated in Tables 12 and 13 and in
the Negligible Impact Determination
later in this proposed rule.
Level A Harassment
Of the potential effects that were
described earlier, following are the
types of effects that can fall into the
Level A harassment category (unless
they further rise to the level of serious
injury or mortality):
Permanent Threshold Shift (PTS)—
PTS (resulting either from exposure to
MFAS/HFAS or explosive detonations)
is irreversible and considered an injury.
PTS results from exposure to intense
sounds that cause a permanent loss of
inner or outer cochlear hair cells or
exceed the elastic limits of certain
tissues and membranes in the middle
and inner ears and result in changes in
the chemical composition of the inner
ear fluids. As mentioned above for TTS,
a stress response is assumed if a
physiological reaction such as a hearing
loss (PTS) or trauma is predicted.
As discussed in the Negligible Impact
Determination later in this proposed
rule, only a small number (5) of Level
A takes resulting from mild levels of
PTS are predicted, and no serious injury
or mortality takes are predicted, with
the Navy’s training activities in the GOA
TMAA.
Tissue Damage due to Acoustically
Mediated Bubble Growth—A few
theories suggest ways in which gas
bubbles become enlarged through
exposure to intense sounds (MFAS/
HFAS) to the point where tissue damage
results. In rectified diffusion, exposure
to a sound field would cause bubbles to
increase in size which could cause
tissue damage that would be considered
injurious. A short duration of sonar
pings (such as that which an animal
exposed to MFAS would be most likely
to encounter) would not likely be long
enough to drive bubble growth to any
substantial size. Alternately, bubbles
could be destabilized by high-level
sound exposures such that bubble
growth then occurs through static
diffusion of gas out of the tissues. The
degree of supersaturation and exposure
levels observed to cause microbubble
destabilization are unlikely to occur,
either alone or in concert because of
how close an animal would need to be
to the sound source to be exposed to
high enough levels, especially
considering the likely avoidance of the
sound source and the required
mitigation. For the reasons above, Level
A harassment in the form of tissue
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9993
damage from acoustically mediated
bubble growth is not predicted for
training activities in the GOA TMAA.
Tissue Damage due to Behaviorally
Mediated Bubble Growth—Several
authors suggest mechanisms in which
marine mammals could behaviorally
respond to exposure to MFAS/HFAS by
altering their dive patterns (unusually
rapid ascent, unusually long series of
surface dives, etc.) in a manner that
might result in unusual bubble
formation or growth ultimately resulting
in tissue damage. In this scenario, the
rate of ascent would need to be
sufficiently rapid to compromise
behavioral or physiological protections
against nitrogen bubble formation.
There is considerable disagreement
among scientists as to the likelihood of
this phenomenon (Piantadosi and
Thalmann, 2004; Evans and Miller,
2003). Although it has been argued that
traumas from recent beaked whale
strandings are consistent with gas
emboli and bubble-induced tissue
separations (Jepson et al., 2003;
´
Fernandez et al., 2005; Fernandez et al.,
2012), nitrogen bubble formation as the
cause of the traumas has not been
verified. If tissue damage does occur by
this phenomenon, it would be
considered an injury. Recent modeling
by Kvadsheim et al. (2012) determined
that while behavioral and physiological
responses to sonar have the potential to
result in bubble formation, the actual
observed behavioral responses of
cetaceans to sonar did not imply any
significantly increased risk over what
may otherwise occur normally in
individual marine mammals. Level A
harassment in the form of tissue damage
from behaviorally mediated bubble
growth is not anticipated for training
activities in the GOA TMAA.
Physical Disruption of Tissues
Resulting from Explosive Shock Wave—
Physical damage of tissues resulting
from a shock wave (from an explosive
detonation) is classified as an injury.
Blast effects are greatest at the gas-liquid
interface (Landsberg, 2000) and gascontaining organs, particularly the lungs
and gastrointestinal tract, are especially
susceptible (Goertner, 1982; Hill 1978;
Yelverton et al., 1973). Nasal sacs,
larynx, pharynx, trachea, and lungs may
be damaged by compression/expansion
caused by the oscillations of the blast
gas bubble (Reidenberg and Laitman,
2003). Severe damage (from the shock
wave) to the ears can include tympanic
membrane rupture, fracture of the
ossicles, damage to the cochlea,
hemorrhage, and cerebrospinal fluid
leakage into the middle ear. Explosions
in the ocean or near the water surface
can introduce loud, impulsive,
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broadband sounds into the marine
environment. These sounds are likely
within the audible range of most marine
mammals, but the duration of
individual sounds is very short. The
direct sound from explosions used
during training activities last less than
a second, and most events involve the
use of only one or a few explosions.
Furthermore, events are dispersed in
time and throughout the GOA TMAA
Study Area. These factors reduce the
likelihood of these sources causing
substantial physical disruption of
tissues in marine mammals, especially
when the avoidance and mitigation
factors are taken into consideration.
Consequently, no Level A harassment
from explosive shock waves is
anticipated from training activities in
the GOA TMAA.
Vessel or Ordnance Strike—Vessel
strike or ordnance strike associated with
the specified activities would be
considered Level A harassment, serious
injury, or mortality. There are no
records of any Navy vessel strikes to
marine mammals during training
activities in the GOA TMMA Study
Area. There have been Navy strikes of
large whales in areas outside the Study
Area, such as Hawaii and Southern
California. However, these areas differ
significantly from the Study Area given
that both Hawaii and Southern
California have a much higher number
of Navy vessel activities and much
higher densities of large whales. The
Navy’s proposed actions would not
result in any appreciable changes in
locations or frequency of vessel activity,
and there have been no whale strikes
during any previous training activities
in the Study Area. The manner in which
the Navy has trained would remain
consistent with the range of variability
observed over the last decade so the
Navy does not anticipate vessel strikes
would occur within the Study Area
during training events. As such, vessel
or ordnance strike is not anticipated
with the Navy activities in the Study
Area and Level A harassment, serious
injury, or mortality are not expected.
Take Thresholds
For the purposes of an MMPA
authorization, three types of take are
identified: Level B harassment; Level A
harassment; and mortality (or serious
injury leading to mortality). The
categories of marine mammal responses
(physiological and behavioral) that fall
into the two harassment categories were
described in the previous section.
Because the physiological and
behavioral responses of the majority of
the marine mammals exposed to nonimpulse and impulse sounds cannot be
easily detected or measured, and
because NMFS must authorize take
prior to the impacts to marine
mammals, a method is needed to
estimate the number of individuals that
will be taken, pursuant to the MMPA,
based on the proposed action. To this
end, NMFS developed acoustic
thresholds that estimate at what
received level (when exposed to nonimpulse or impulse sounds) Level B
harassment and Level A harassment of
marine mammals would occur. The
acoustic thresholds for non-impulse and
impulse sounds are discussed below.
Level B Harassment Threshold
(TTS)—Behavioral disturbance, acoustic
masking, and TTS are all considered
Level B harassment. Marine mammals
would usually be behaviorally disturbed
at lower received levels than those at
which they would likely sustain TTS, so
the levels at which behavioral
disturbance are likely to occur is
considered the onset of Level B
harassment. The behavioral responses of
marine mammals to sound are variable,
context specific, and, therefore, difficult
to quantify (see Risk Function section,
below).
TTS is a physiological effect that has
been studied and quantified in
laboratory conditions. Because data
exist to support an estimate of the
received levels at which marine
mammals will incur TTS, NMFS uses an
acoustic criteria to estimate the number
of marine mammals that might sustain
TTS. TTS is a subset of Level B
harassment (along with sub-TTS
behavioral harassment) and the Navy is
not specifically required to estimate
those numbers; however, the more
specifically the affected marine mammal
responses can be estimated, the better
the analysis.
Level A Harassment Threshold
(PTS)—For acoustic effects, because the
tissues of the ear appear to be the most
susceptible to the physiological effects
of sound, and because threshold shifts
tend to occur at lower exposures than
other more serious auditory effects,
NMFS has determined that PTS is the
best indicator for the smallest degree of
injury that can be measured. Therefore,
the acoustic exposure associated with
onset-PTS is used to define the lower
limit of Level A harassment.
PTS data do not currently exist for
marine mammals and are unlikely to be
obtained due to ethical concerns.
However, PTS levels for these animals
may be estimated using TTS data from
marine mammals and relationships
between TTS and PTS that have been
determined through study of terrestrial
mammals.
We note here that behaviorally
mediated injuries (such as those that
have been hypothesized as the cause of
some beaked whale strandings) could
potentially occur in response to
received levels lower than those
believed to directly result in tissue
damage. As mentioned previously, data
to support a quantitative estimate of
these potential effects (for which the
exact mechanism is not known and in
which factors other than received level
may play a significant role) do not exist.
However, based on the number of years
(more than 60) and number of hours of
MFAS per year that the U.S. (and other
countries) has operated compared to the
reported (and verified) cases of
associated marine mammal strandings,
NMFS believes that the probability of
these types of injuries is very low.
Tables 9 and 10 provide a summary of
non-impulsive and impulsive
thresholds to TTS and PTS for marine
mammals. A detailed explanation of
how these thresholds were derived is
provided in the Criteria and Thresholds
Technical Report (Finneran and Jenkins,
2012) and summarized in Chapter 6 of
the LOA application (https://
www.nmfs.noaa.gov/pr/permits/
incidental/military.htm).
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TABLE 9—ONSET TTS AND PTS THRESHOLDS FOR NON-IMPULSE SOUND
Group
Species
Onset TTS
Low-Frequency Cetaceans ............
Mid-Frequency Cetaceans .............
All mysticetes ................................
Most delphinids, beaked whales,
medium and large toothed
whales.
Porpoises, Kogia spp. ..................
Harbor, Hawaiian monk, elephant
seals.
178 dB re 1μPa2-sec(LFII) ...........
178 dB re 1μPa2-sec(MFII) ..........
198 dB re 1μPa2-sec(LFII).
198 dB re 1μPa2-sec(MFII).
152 dB re 1μPa2-sec(HFII) ..........
183 dB re 1μPa2-sec(PWI) ...........
172 dB re 1μPa2-secSEL (HFII).
197 dB re 1μPa2-sec(PWI).
High-Frequency Cetaceans ...........
Phocidae In-water ..........................
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TABLE 9—ONSET TTS AND PTS THRESHOLDS FOR NON-IMPULSE SOUND—Continued
Group
Species
Onset TTS
Onset PTS
Otariidae & Obodenidae In-water ..
Mustelidae In-water .......................
Sea lions and fur seals .................
Sea otters.
206 dB re 1μPa2-sec(OWI) ...........
220 dB re 1μPa2-sec(OWI).
LFII, MFII, HFII: New compound Type II weighting functions; PWI, OWI: Original Type I (Southall et al., 2007) for pinniped and mustelid in water.
Table 10. Impulsive sound explosive criteria and thresholds for predicting injury and mortality.
Group
Species
Onset TTS
Low
Frequency
Cetaceans
All mysticetes
MidFrequency
Cetaceans
Most
delphinids,
medium and
large toothed
whales
High
Frequency
Cetaceans
Porpoises and
Kogia spp.
Phocidae
Northern
elephant seal
and harbor
seal
Otariidae
Steller and
California Sea
Lion,
Guadalupe
and Northern
fur seal
Mustelidae
Onset Slight
Lung
Injury
Onset
Mortality
237 dB
re 1 11Pa
(unweighted)
Note 1
Note2
187 dB re 1 11Pa2-s SEL
(Type II weighting)
or
230 dB re 1 11Pa Peak
SPL
(unweighted)
187 dB re 1 11Pa2-s SEL
(Type II weighting)
or
230 dB re 1 11Pa Peak
SPL
(unweighted)
161 dB re 1 11Pa2-s SEL
(Type II weighting)
or
201 dB re 1 11Pa Peak
SPL
(unweighted)
192 dB re 1 11Pa2-s
(Type I weighting)
or
218 dB re l11PaPeak
SPL
(unweighted)
215 dB re 1 11Pa2-s
(Type I weighting)
or
218 dB re l11PaPeak
SPL
(unweighted)
Sea Otter
Note 1 = 39 .1M
X(1 + 10.081
D
t
_____B!!!._
P a - sec
Note2
= 9l.4M
X(1 + D y~ Pa- sec
____l!!!:_
10.081
Impulse calculated over a dehvery t1me that 1s the lesser of the m1hal pos1t1Ve pressure durat10n or 20 percent of the natural
period of the assumed-spherical lung adjusted for animal size and depth.
Notes: GI =gastrointestinal, M =mass of animals in kilograms, DRrn =depth of receiver (animal) in meters, SEL =Sound
Exposure Level, SPL = Sound Pressure Level (re 1 11Pa), dB= decibels, re 1 11Pa =referenced to one micropascal, dB re 1 11Pa2-s
= decibels referenced to one micropascal squared second
Level B Harassment Risk Function
(Behavioral Harassment)
As the statutory definition is currently
applied, a wide range of behavioral
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reactions may qualify as Level B
harassment under the MMPA, including
but not limited to avoidance of the
sound source, temporary changes in
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vocalizations or dive patters, temporary
avoidance of an area, or temporary
disruption of feeding, migrating, or
reproductive behaviors. The estimates
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172 dB re 1 11Pa2-s
SEL
(Type II weighting)
or
224 dB re 1 11Pa Peak
SPL
(unweighted)
172 dB re 1 11Pa2-s
SEL
(Type II weighting)
or
224 dB re 1 11Pa Peak
SPL
(unweighted)
146 dB re 1 11Pa2-s
SEL
(Type II weighting)
or
195 dB re 1 11Pa Peak
SPL
(unweighted)
177 dB re 1 11Pa2-s
(Type I weighting)
or
212 dB re 1 11Pa Peak
SPL
(unweighted)
200 dB re 1 11Pa2-s
(Type I weighting)
or
212 dB re 1 11Pa Peak
SPL
(unweighted)
Onset Slight
GI Tract
Injury
OnsetPTS
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calculated by the Navy using the
acoustic thresholds do not differentiate
between the different types of potential
behavioral reactions. Nor do the
estimates provide information regarding
the potential fitness or other biological
consequences of the reactions on the
affected individuals. We therefore
consider the available scientific
evidence to determine the likely nature
of the modeled behavioral responses
and the potential fitness consequences
for affected individuals.
Behavioral Response Criteria for NonImpulsive Sound from Sonar and other
Active Sources—In 2006, NMFS issued
the first MMPA authorization to allow
the take of marine mammals incidental
to MFAS (to the Navy for RIMPAC). For
that authorization, NMFS used 173 dB
SEL as the criterion for the onset of
behavioral harassment (Level B
harassment). This type of single number
criterion is referred to as a step function,
in which (in this example) all animals
estimated to be exposed to received
levels above 173 db SEL would be
predicted to be taken by Level B
Harassment and all animals exposed to
less than 173 dB SEL would not be
taken by Level B harassment. As
mentioned previously, marine mammal
behavioral responses to sound are
highly variable and context specific
(affected by differences in acoustic
conditions; differences between species
and populations; differences in gender,
age, reproductive status, or social
behavior; or the prior experience of the
individuals), which means that there is
support for alternate approaches for
estimating behavioral harassment.
Unlike step functions, acoustic risk
continuum functions (which are also
called ‘‘exposure-response functions’’ or
‘‘dose-response functions’’ in other risk
assessment contexts) allow for
probability of a response that NMFS
would classify as harassment to occur
over a range of possible received levels
(instead of one number) and assume that
the probability of a response depends
first on the ‘‘dose’’ (in this case, the
received level of sound) and that the
probability of a response increases as
the ‘‘dose’’ increases. In January 2009,
NMFS issued three final rules governing
the incidental take of marine mammals
(within Navy’s Hawaii Range, Southern
California Training and Testing Range,
and Atlantic Fleet Active Sonar
Training complexes) that used a risk
continuum to estimate the percent of
marine mammals exposed to various
levels of MFAS that would respond in
a manner NMFS considers harassment.
The Navy and NMFS have previously
used acoustic risk functions to estimate
the probable responses of marine
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mammals to acoustic exposures for
other training and research programs.
Examples of previous application
include the Navy FEISs on the
Surveillance Towed Array Sensor
System Low Frequency Active
(SURTASS LFA) sonar (U.S. Department
of the Navy, 2001c); the North Pacific
Acoustic Laboratory experiments
conducted off the Island of Kauai (Office
of Naval Research, 2001), and the
Supplemental EIS for SURTASS LFA
sonar (U.S. Department of the Navy,
2007d). As discussed earlier, factors
other than received level (such as
distance from or bearing to the sound
source, context of animal at time of
exposure) can affect the way that marine
mammals respond; however, data to
support a quantitative analysis of those
(and other factors) do not currently
exist. It is also worth specifically noting
that while context is very important in
marine mammal response, given
otherwise equivalent context, the
severity of a marine mammal behavioral
response is also expected to increase
with received level (Houser and Moore,
2014). NMFS will continue to modify
these criteria as new data become
available and can be appropriately and
effectively incorporated.
The particular acoustic risk functions
developed by NMFS and the Navy (see
Figures 1 and 2 of the LOA application)
estimate the probability of behavioral
responses to MFAS/HFAS (interpreted
as the percentage of the exposed
population) that NMFS would classify
as harassment for the purposes of the
MMPA given exposure to specific
received levels of MFAS/HFAS. The
mathematical function (below)
underlying this curve is a cumulative
probability distribution adapted from a
solution in Feller (1968) and was also
used in predicting risk for the Navy’s
SURTASS LFA MMPA authorization as
well.
Where:
R = Risk (0—1.0)
L = Received level (dB re: 1 mPa)
B = Basement received level = 120 dB re: 1
mPa
K = Received level increment above B where
50-percent risk = 45 dB re: 1 mPa
A = Risk transition sharpness parameter = 10
(odontocetes and pinnipeds) or 8
(mysticetes)
Detailed information on the above
equation and its parameters is available
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in the LOA application and previous
Navy documents listed above.
The harbor porpoise and beaked
whales have unique criteria based on
specific data that show these animals to
be especially sensitive to sound. Harbor
porpoise and beaked whale nonimpulsive behavioral criteria are used
unweighted—without weighting the
received level before comparing it to the
threshold (see Finneran and Jenkins,
2012).
It has been speculated for some time
that beaked whales might have unusual
sensitivities to sonar sound due to their
likelihood of stranding in conjunction
with mid-frequency sonar use, even in
areas where other species were more
abundant (D’Amico et al., 2009), but
there were not sufficient data to support
a separate treatment for beaked whales
until recently. With the recent
publication of results from Blainville’s
beaked whale monitoring and
experimental exposure studies on the
instrumented AUTEC range in the
Bahamas (McCarthy et al. 2011; Tyack
et al. 2011), there are now statistically
strong data suggesting that beaked
whales tend to avoid actual naval midfrequency sonar in real anti-submarine
training scenarios as well as playbacks
of killer whale vocalizations, and other
anthropogenic sounds. Tyack et al.
(2011) report that, in reaction to sonar
playbacks, most beaked whales stopped
echolocating, made long slow ascent,
and moved away from the sound.
During an exercise using mid-frequency
sonar, beaked whales avoided the sonar
acoustic footprint at a distance where
the received level was ‘‘around 140 dB’’
(SPL) and once the exercise ended,
beaked whales re-inhabited the center of
exercise area within 2–3 days (Tyack et
al., 2011). The Navy has therefore
adopted an unweighted 140 dB re 1 mPa
SPL threshold for significant behavioral
effects for all beaked whales (family:
Ziphiidae).
Since the development of the
criterion, analysis of the data the 2010
and 2011 field seasons of the southern
California Behavioral Responses Study
have been published. The study,
DeRuiter et al. (2013b), provides similar
evidence of Cuvier’s beaked whale
sensitivities to sound based on two
controlled exposures. Two whales, one
in each season, were tagged and
exposed to simulated mid-frequency
active sonar at distances of 3.4–9.5 km.
The 2011 whale was also incidentally
exposed to mid-frequency active sonar
from a distant naval exercise
(approximately 118 km away). Received
levels from the mid-frequency active
sonar signals during the controlled and
incidental exposures were calculated as
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84–144 and 78–106 dB re 1 mPa rms,
respectively. Both whales showed
responses to the controlled exposures,
ranging from initial orientation changes
to avoidance responses characterized by
energetic fluking and swimming away
from the source. However, the authors
did not detect similar responses to
incidental exposure to distant naval
sonar exercises at comparable received
levels, indicating that context of the
exposures (e.g., source proximity,
controlled source ramp-up) may have
been a significant factor. Because the
sample size was limited (controlled
exposures during a single dive in both
2010 and 2011) and baseline behavioral
data was obtained from different stocks
and geographic areas (i.e., Hawaii and
Mediterranean Sea), and the responses
exhibited to controlled exposures were
not exhibited by an animal exposed to
some of the same received levels of real
sonar exercises, the Navy relied on the
studies at the AUTEC that analyzed
beaked whale responses to actual naval
exercises using mid-frequency active
sonar to evaluate potential behavioral
responses by beaked whales to proposed
training and testing activities using
sonar and other active acoustic sources.
The information currently available
regarding harbor porpoises suggests a
very low threshold level of response for
both captive and wild animals.
Threshold levels at which both captive
(Kastelein et al., 2000; Kastelein et al.,
2005; Kastelein et al., 2006; Kastelein et
al., 2008) and wild harbor porpoises
(Johnston, 2002) responded to sound
(e.g., acoustic harassment devices,
acoustic deterrent devices, or other nonimpulsive sound sources) are very low
(e.g., approximately 120 dB re 1 mPa).
Therefore, a SPL of 120 dB re 1 mPa is
used in this analysis as a threshold for
predicting behavioral responses in
harbor porpoises instead of the risk
functions used for other species (i.e., we
assume for the purpose of estimating
take that all harbor porpoises exposed to
120 dB or higher MFAS/HFAS will be
taken by Level B behavioral
harassment).
Behavioral Response Criteria for
Impulsive Sound from Explosions — If
more than one explosive event occurs
within any given 24-hour period within
a training or testing event, behavioral
criteria are applied to predict the
number of animals that may be taken by
Level B harassment. For multiple
explosive events the behavioral
threshold used in this analysis is 5 dB
less than the TTS onset threshold (in
sound exposure level). This value is
derived from observed onsets of
behavioral response by test subjects
(bottlenose dolphins) during nonimpulse TTS testing (Schlundt et al.,
2000). Some multiple explosive events,
such as certain naval gunnery exercises,
may be treated as a single impulsive
event because a few explosions occur
closely spaced within a very short
period of time (a few seconds). For
single impulses at received sound levels
below hearing loss thresholds, the most
likely behavioral response is a brief
alerting or orienting response. Since no
further sounds follow the initial brief
impulses, Level B take in the form of
behavioral harassment beyond that
associated with potential TTS would
not be expected to occur. This reasoning
was applied to previous shock trials (63
9997
FR 230; 66 FR 87; 73 FR 143) and is
extended to these Phase 2 criteria.
Behavioral thresholds for impulsive
sources are summarized in Table 11 and
further detailed in the LOA application.
Since impulse events can be quite
short, it may be possible to accumulate
multiple received impulses at sound
pressure levels considerably above the
energy-based criterion and still not be
considered a behavioral take. The Navy
treats all individual received impulses
as if they were one second long for the
purposes of calculating cumulative
sound exposure level for multiple
impulse events. For example, five air
gun impulses, each 0.1 second long,
received at a Type II weighted sound
pressure level of 167 dB SPL would
equal a 164 dB sound exposure level,
and would not be predicted as leading
to a significant behavioral response
(take) in MF or HF cetaceans. However,
if the five 0.1 second pulses are treated
as a 5 second exposure, it would yield
an adjusted SEL of approximately 169
dB, exceeding the behavioral threshold
of 167 dB SEL. For impulses associated
with explosions that have durations of
a few microseconds, this assumption
greatly overestimates effects based on
sound exposure level metrics such as
TTS and PTS and behavioral responses.
Appropriate weighting values will be
applied to the received impulse in onethird octave bands and the energy
summed to produce a total weighted
sound exposure level value. For
impulsive behavioral criteria, the Navy’s
weighting functions (detailed in Chapter
6 of the LOA application) are applied to
the received sound level before being
compared to the threshold.
TABLE 11—BEHAVIORAL THRESHOLDS FOR IMPULSIVE SOUND
Impulsive behavioral threshold for > 2 pulses/
24 hours
Hearing group
Low-Frequency Cetaceans ................................
Mid-Frequency Cetaceans .................................
High-Frequency Cetaceans ...............................
Phocid Seals (in water) ......................................
Otariidae & Mustelidae (in water) ......................
167
167
141
172
195
dB
dB
dB
dB
dB
SEL
SEL
SEL
SEL
SEL
(LFII) ............................................
(MFII).
(HFII) ............................................
(PWI) ............................................
(OWI) ............................................
Onset TTS
172 dB SEL (MFII) or 224 dB Peak SPL.
146 dB SEL (HFII) or 195 dB Peak SPL.
177 dB SEL (PWI) or 212 dB Peak SPL.
200 dB SEL (OWI) or 212 dB Peak SPL.
Notes: (1) LFII, MFII, HFII are New compound Type II weighting functions; PWI, OWI = Original Type I (Southall et al., 2007) for pinniped and
mustelid in water (see Finneran and Jenkins 2012). (2) SEL = re 1 μPa2¥s; SPL = re 1 μPa, SEL = Sound Exposure Level, dB = decibel, SPL =
Sound Pressure Level.
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Marine Mammal Density Estimates
A quantitative impact analysis
requires an estimate of the number of
animals that might be affected by
anthropogenic activities. A key element
of this estimation is knowledge of the
abundance and concentration of the
species in specific areas where those
activities will occur. The most
appropriate unit of metric for this type
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of analysis is animal density, or the
number of animals present per unit area.
Marine species density estimation
requires a significant amount of effort to
both collect and analyze data to produce
a reasonable estimate. Unlike surveys
for terrestrial wildlife, many marine
species spend much of their time
submerged, and are not easily observed.
In order to collect enough sighting data
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to make reasonable density estimates,
multiple observations are required,
often in areas that are not easily
accessible (e.g., far offshore). Ideally,
marine species sighting data would be
collected for the specific area and time
period (e.g., season) of interest and
density estimates derived accordingly.
However, in many places, poor weather
conditions and high sea states prohibit
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the completion of comprehensive visual
surveys.
For most cetacean species, abundance
is estimated using line-transect surveys
or mark-recapture studies (e.g., Barlow,
2010, Barlow and Forney, 2007,
Calambokidis et al., 2008). The result
provides one single density estimate
value for each species across broad
geographic areas, such as waters within
the U.S. EEZ off California, Oregon, and
Washington. This is the general
approach applied in estimating cetacean
abundance in the NMFS Stock
Assessment Reports. Although the
single value provides a good average
estimate of abundance (total number of
individuals) for a specified area, it does
not provide information on the species
distribution or concentrations within
that area, and it does not estimate
density for other timeframes or seasons
that were not surveyed. More recently,
habitat modeling has been used to
estimate cetacean densities (Barlow et
al., 2009; Becker et al., 2010, 2012a, b,
c; Ferguson et al., 2006a; Forney et al.,
2012; Redfern et al., 2006). These
models estimate cetacean density as a
continuous function of habitat variables
(e.g., sea surface temperature, seafloor
depth, etc.) and thus allow predictions
of cetacean densities on finer spatial
scales than traditional line-transect or
mark-recapture analyses. Within the
geographic area that was modeled,
densities can be predicted wherever
these habitat variables can be measured
or estimated.
Uncertainty in published density
estimates is typically large because of
the low number of sightings available
for their derivation. Uncertainty is
typically expressed by the coefficient of
variation (CV) of the estimate, which is
derived using standard statistical
methods and describes the amount of
variation with respect to the population
mean. It is expressed as a fraction or
sometimes a percentage and can range
upward from zero, indicating no
uncertainty, to high values. For
example, a CV of 0.85 would indicate
high uncertainty in the population
estimate. When the CV exceeds 1.0, the
estimate is very uncertain. The
uncertainty associated with movements
of animals into or out of an area (due to
factors such as availability of prey or
changing oceanographic conditions) is
much larger than is indicated by the CV.
The methods used to estimate
pinniped at-sea densities are typically
different than those used for cetaceans.
This is discussed in more detail in the
Navy Marine Species Density Database
Technical Report (U.S. Department of
the Navy, 2014). Pinniped abundance is
generally estimated via shore counts of
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animals at known rookeries and haulout
sites. Translating these numbers to inwater densities is difficult given the
variability in foraging ranges, migration,
and haulout behavior between species
and within each species, and is driven
by factors such as age class, sex class,
seasonal variation, etc. Details of the
density derivation for each species of
pinniped in the Study Area are
provided in the U.S. Department of the
Navy (2014). In summary, the methods
used to derive pinniped densities
involved a series of species-specific data
reviews to compile the most accurate
and up-to-date information available.
The total abundance divided by the area
of the region was the resultant density
estimate for each species in a given
location.
There is no single source of density
data for every area, marine mammal
species, and season because of the fiscal
costs, resources, and effort involved to
provide enough survey coverage to
sufficiently estimate density. NMFS
Southwest Fisheries Science Center
conducts standard U.S. West Coast
surveys every 5–6 years and cannot
logistically support more frequent
studies. The U.S. Navy has funded two
previous marine mammal surveys in the
GOA TMAA (Rone et al., 2009, 2014) in
the summer time-period when Navy
training activities are most likely to
occur. The density data used to
quantitatively estimate impacts to
marine mammals from Navy training in
the GOA TMAA are based on the best
available science and were agreed upon
with NMFS as a cooperating agency for
the SEIS/OEIS. As the federal regulator
for the MMPA, the NMFS role included
having staff biologists review and
comment on the analysis and the SEIS/
OEIS. The review also included
coordination with NMFS regional
scientists from the Southwest Fisheries
Science Center and Alaska Fisheries
Science Center on the latest emergent
data presented in their Pacific Stock
Assessment Reports.
In May 2015, the Marine Mammal
Commission also reviewed the Marine
Species Density Database Technical
Report (U.S. Department of the Navy,
2014) and pointed out some textual
errors that the Navy subsequently
corrected, but otherwise did not identify
any changes in the data used for
acoustic effects modeling.
A certain number of sightings are
required to generate the quality of data
necessary to produce either traditional
line-transect density estimates or spatial
habitat modeled density values. The atsea identification of some species of
specific MMPA designated stocks is not
always possible from available field
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data, nor would additional data
collection likely address the
identification issue based on low animal
occurrence (e.g., Western North Pacific
gray whale), cryptic behaviors (e.g.,
beaked whales), and appearance
similarities between stocks (e.g., Steller
sea lions). In the absence of speciesspecific population survey data for these
species, density estimates are derived
from different methods and data
sources, based on NMFS
recommendations. The different
methods for each of these species are
described in Section 3.8.3.1.6.1 (Marine
Species Density Data) of the DSEIS/
OEIS and the Marine Species Density
Database Technical Report (U.S.
Department of the Navy, 2014). NMFS
and Navy have determined that these
alternative density estimates are
sufficient for determining the impacts of
Navy training on these marine mammals
under all applicable statutes, and
therefore are the best available science.
Therefore, to characterize marine
mammal density for areas of concern,
including the GOA TMAA Study Area,
the Navy compiled data from multiple
sources. Each data source may use
different methods to estimate density
and uncertainty (e.g., variance)
associated with the estimates.
The Navy thus developed a protocol
to select the best available data sources
based on species, area, and time
(season). The Navy then used this
protocol to identify the best density data
from available sources, including
habitat-based density models, linetransect analyses, and peer-reviewed
published studies. These data were
incorporated into a Geographic
Information System database that
includes seasonal (summer/fall and
winter/spring) density values for every
marine mammal species present within
the Study Area. Detailed information on
the Navy’s selection protocol, datasets,
and specific density values are provided
in the Navy Marine Species Density
Database Technical Report (U.S.
Department of the Navy, 2014).
Quantitative Modeling To Estimate Take
for Impulsive and Non-Impulsive Sound
The Navy performed a quantitative
analysis to estimate the number of
marine mammals that could be affected
by acoustic sources or explosives used
during Navy training activities. Inputs
to the quantitative analysis include
marine mammal density estimates;
marine mammal depth occurrence
distributions; oceanographic and
environmental data; marine mammal
hearing data; and criteria and thresholds
for levels of potential effects. The
quantitative analysis consists of
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computer modeled estimates and a postmodel analysis to determine the number
of potential mortalities and
harassments. The model calculates
sound energy propagation from sonar,
other active acoustic sources, and
explosives during naval activities; the
sound or impulse received by animat
(virtual representation of an animal)
dosimeters representing marine
mammals distributed in the area around
the modeled activity; and whether the
sound or impulse received by a marine
mammal exceeds the thresholds for
effects. The model estimates are then
further analyzed to consider animal
avoidance and implementation of
mitigation measures, resulting in final
estimates of potential effects due to
Navy training.
Various computer models and
mathematical equations can be used to
predict how energy spreads from a
sound source (e.g., sonar or underwater
detonation) to a receiver (e.g., dolphin
or sea turtle). Basic underwater sound
models calculate the overlap of energy
and marine life using assumptions that
account for the many, variable, and
often unknown factors that can
influence the result. Assumptions in
previous and current Navy models have
intentionally erred on the side of
overestimation when there are
unknowns or when the addition of other
variables was not likely to substantively
change the final analysis. For example,
because the ocean environment is
extremely dynamic and information is
often limited to a synthesis of data
gathered over wide areas and requiring
many years of research, known
information tends to be an average of a
˜
seasonal or annual variation. El Nino
Southern Oscillation events of the
ocean-atmosphere system are an
example of dynamic change where
unusually warm or cold ocean
temperatures are likely to redistribute
marine life and alter the propagation of
underwater sound energy. Previous
Navy modeling therefore made some
assumptions indicative of a maximum
theoretical propagation for sound energy
(such as a perfectly reflective ocean
surface and a flat seafloor).
More complex computer models build
upon basic modeling by factoring in
additional variables in an effort to be
more accurate by accounting for such
things as variable bathymetry and an
animal’s likely presence at various
depths.
The Navy has developed new
software tools, up to date marine
mammal density data, and other
oceanographic data for the
quantification of estimated acoustic
impacts to marine mammal impacts
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from Navy activities. This new approach
is the resulting evolution of the basic
model previously used by the Navy and
reflects a more complex modeling
approach as described below. The new
model, NAEMO, is the standard model
now used by the navy to estimate the
potential acoustic effects of Navy
training and testing activities on marine
mammals. Although this more complex
computer modeling approach accounts
for various environmental factors
affecting acoustic propagation, the
current software tools do not consider
the likelihood that a marine mammal
would attempt to avoid repeated
exposures to a sound or avoid an area
of intense activity where a training or
testing event may be focused.
Additionally, the software tools do not
consider the implementation of
mitigation (e.g., stopping sonar
transmissions when a marine mammal
is within a certain distance of a ship or
mitigation zone clearance prior to
detonations). In both of these situations,
naval activities are modeled as though
an activity would occur regardless of
proximity to marine mammals and
without any horizontal movement by
the animal away from the sound source
or human activities. Therefore, the final
step of the quantitative analysis of
acoustic effects is to consider the
implementation of mitigation and the
possibility that marine mammals would
avoid continued or repeated sound
exposures. This final, post-analysis step
in the modeling process is meant to
better quantify the predicted effects by
accounting for likely animal avoidance
behavior and implementation of
standard Navy mitigations.
The incorporation of mitigation
factors for the reduction of predicted
effects used a conservative approach
(erring on the side of overestimating the
number of effects) since reductions as a
result of implemented mitigation were
only applied to those events having a
very high likelihood of detecting marine
mammals.
The steps of the quantitative analysis
of acoustic effects, the values and
assumptions that went into the Navy’s
model, and the resulting ranges to
effects are detailed in Chapter 6 (Section
6.5) of the LOA application (https://
www.nmfs.noaa.gov/pr/permits/
incidental/). Details of the model’s
processes and the description and
derivation of the inputs are presented in
the Navy’s Determination of Acoustic
Effects technical Report (Marine Species
Modeling Team, 2014). The post-model
analysis, which considers the potential
for avoidance and highly effective
mitigation during the use of sonar and
other active acoustic sources and
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9999
explosives, is described in Section 6.5 of
the LOA application. A detailed
explanation of the post-model acoustic
effect analysis quantification process is
also provided in the technical report
Post-Model Quantitative Analysis of
Animal Avoidance Behavior and
Mitigation Effectiveness for the Gulf of
Alaska Training (U.S. Department of the
Navy, 2014c; also available at: https://
goaeis.com/Documents/Supplemental
EISOEISDocumentsandReferences/
SupportingTechnicalDocuments.aspx).
Take Request
The GOA DSEIS/OEIS considered all
training activities proposed to occur in
the Study Area that have the potential
to result in the MMPA defined take of
marine mammals. The stressors
associated with these activities included
the following:
• Acoustic (sonar and other active
non-impulse sources, explosives,
swimmer defense airguns, weapons
firing, launch and impact noise, vessel
noise, aircraft noise);
• Energy (electromagnetic devices);
• Physical disturbance or strikes
(vessels, in-water devices, military
expended materials, seafloor devices);
• Entanglement (fiber optic cables,
guidance wires, parachutes);
• Ingestion (munitions, military
expended materials other than
munitions); and
• Secondary stressors (sediments and
water quality).
The Navy determined, and NMFS
agrees, that two stressors could
potentially result in the incidental
taking of marine mammals from training
activities within the Study Area: (1)
Non-impulsive stressors (sonar and
other active acoustic sources) and (2)
impulsive stressors (explosives). Nonimpulsive and impulsive stressors have
the potential to result in incidental takes
of marine mammals by harassment,
injury, or mortality.
Training Activities
A detailed analysis of effects due to
marine mammal exposures to impulsive
and non-impulsive sources in the Study
Area is presented in Chapter 6 of the
LOA application. Based on the model
and post-model analysis described in
Chapter 6 of the LOA application, Table
12 summarizes the Navy’s final take
request for training activities for a year
(up to 2 exercises occurring over a 7month period [April–October]) and the
summation over a 5-year period (up to
2 exercises occurring over a 7-month
period [April–October] for a total of 10
exercises).
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TABLE 12—SUMMARY OF ANNUAL AND 5-YEAR TAKE REQUESTS FOR GOA TMAA TRAINING ACTIVITIES
Training activities
MMPA Category
Source
Annual authorization sought
Mortality .........................................
Level A ...........................................
Level B ...........................................
Explosives .....................................
Sonar and other active acoustic
sources; explosives.
Sonar and other active acoustic
sources; explosives.
Impulsive and Non-Impulsive Sources
Table 13 provides details on the
Navy’s final take request for training
activities by species from the acoustic
5-Year authorization sought
0 ....................................................
5 (Dall’s porpoise only as shown
in Table 13).
36,522 (Species specific data
shown in Table 13).
0.
25 (Dall’s porpoise only as shown
in Table 13).
182,610 (Species specific data
shown in Table 13).
effects modeling estimates. Derivations
of the numbers presented in Table 13
are described in more detail within
Chapter 6 of the LOA application. Level
A effects are only predicted to occur for
Dall’s porpoises. There are no
mortalities predicted for any of the
proposed training activities.
TABLE 13—SPECIES-SPECIFIC TAKE REQUESTS FROM MODELING ESTIMATES OF IMPULSIVE AND NON-IMPULSIVE SOURCE
EFFECTS FOR ALL TRAINING ACTIVITIES
Annual
Species
Level B
North Pacific right whale ...................
Humpback whale ..............................
Level A
Level B
Level A
7
129
10
95
0
2,582
13
87
0
0
197
564
53
1
144
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
35
645
50
475
0
12,910
65
435
0
0
985
2,820
265
5
720
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Ribbon seal .......................................
Eastern North Pacific .......................
Central North Pacific ........................
Western North Pacific ......................
Eastern North Pacific .......................
Central North Pacific ........................
Northeast Pacific ..............................
Eastern North Pacific .......................
Alaska ...............................................
Eastern North Pacific .......................
Western North Pacific ......................
North Pacific .....................................
Alaska Resident ...............................
Eastern North Pacific Offshore ........
AT1 Transient ...................................
GOA, Aleutian Island, and Bearing
Sea Transient.
North Pacific .....................................
Gulf of Alaska ...................................
Southeast Alaska .............................
Alaska ...............................................
Alaska ...............................................
Alaska ...............................................
Alaska ...............................................
Eastern U.S. .....................................
Western U.S. ....................................
U.S. ..................................................
Eastern Pacific-Alaska .....................
California Breeding ...........................
Aleutian Islands ................................
Pribilof Islands ..................................
Bristol Bay ........................................
North Kodiak ....................................
South Kodiak ....................................
Prince William Sound .......................
Cook Inlet/Shelikof ...........................
Glacier Bay/Icy Strait .......................
Lynn Canal/Stephens .......................
Sitka/Chatham ..................................
Dixon/Cape Decision ........................
Clarence Strait .................................
Alaska ...............................................
1,963
5,484
1,926
16,244
2,544
401
1,153
671
572
5
1,428
245
0
0
0
1
1
2
0
0
0
0
0
0
0
0
0
0
5
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
9,815
27,420
9,630
81,220
12,720
2,005
5,765
3,355
2,860
25
7,140
1,225
0
0
0
5
5
10
0
0
0
0
0
0
0
0
0
0
25
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
Totals .........................................
...........................................................
36,522
5
182,610
25
Blue whale ........................................
Fin whale ...........................................
Sei whale ..........................................
Minke whale ......................................
Gray whale ........................................
Sperm whale .....................................
Killer whale ........................................
Pacific white-sided dolphin ...............
Harbor porpoise ................................
Dall’s porpoise ..................................
Cuvier’s beaked whale ......................
Baird’s beaked whale ........................
Stejneger’s beaked whale .................
Steller sea lion ..................................
California sea lion .............................
Northern fur seal ...............................
Northern elephant seal .....................
Harbor seal .......................................
Harbor seal .......................................
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5-Year
Stock
Marine Mammal Habitat
The Navy’s proposed training
activities could potentially affect marine
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mammal habitat through the
introduction of sound into the water
column, impacts to the prey species of
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marine mammals, bottom disturbance,
or changes in water quality. Each of
these components was considered in the
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GOA DSEIS/OEIS and was determined
by the Navy to have no effect on marine
mammal habitat. Based on the
information below and the supporting
information included in the GOA
DSEIS/OEIS, NMFS has preliminarily
determined that the proposed training
activities would not have adverse or
long-term impacts on marine mammal
habitat.
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Expected Effects on Habitat
Unless the sound source or explosive
detonation is stationary and/or
continuous over a long duration in one
area, the effects of the introduction of
sound into the environment are
generally considered to have a less
severe impact on marine mammal
habitat than the physical alteration of
the habitat. Acoustic exposures are not
expected to result in long-term physical
alteration of the water column or bottom
topography, as the occurrences are of
limited duration and are intermittent in
time. Surface vessels associated with the
activities are present in limited duration
and are intermittent as they move
relatively rapidly through any given
area. Most of the high-explosive military
expended materials would detonate at
or near the water surface. Only bottomlaid explosives are likely to affect
bottom substrate; habitat used for
underwater detonations and seafloor
device placement would primarily be
soft-bottom sediment. Once on the
seafloor, military expended material
would likely be colonized by benthic
organisms because the materials would
serve as anchor points in the shifting
bottom substrates, similar to a reef. The
surface area of bottom substrate affected
would make up a very small percentage
of the total training area available in the
Study Area.
Effects on Marine Mammal Prey
Invertebrates—Marine invertebrate
distribution in the Study Area is
influenced by habitat, ocean currents,
and water quality factors such as
temperature, salinity, and nutrient
content (Levinton 2009). The
distribution of invertebrates is also
influenced by their distance from the
equator (latitude); in general, the
number of marine invertebrate species
increases toward the equator
(Macpherson 2002). The higher number
of species (diversity) and abundance of
marine invertebrates in coastal habitats,
compared with the open ocean, is a
result of more nutrient availability from
terrestrial environments and the variety
of habitats and substrates found in
coastal waters (Levinton 2009).
The GOA is one of the world’s most
productive ocean regions and the
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habitats associated with these cold and
turbulent waters contain identifiable
collections of macrohabitats that sustain
a multitude of invertebrate species.
Invertebrates in the GOA provide
valuable links in the food chain and
perform ecosystem functions such as
nutrient processing. For humans,
invertebrates contribute to economic,
cultural, and recreational activities in
the GOA.
All marine invertebrate taxonomic
groups are represented in the Study
Area. Major invertebrate phyla and the
general zones they inhabit in the Study
Area are described in Chapter 3 of the
2011 GOA FEIS/OEIS.
Very little is known about sound
detection and use of sound by aquatic
invertebrates (Budelmann 2010;
Montgomery et al., 2006; Popper et al.,
2001). Organisms may detect sound by
sensing either the particle motion or
pressure component of sound, or both.
Aquatic invertebrates probably do not
detect pressure since many are generally
the same density as water and few, if
any, have air cavities that would
function like the fish swim bladder in
responding to pressure (Budelmann,
2010; Popper et al., 2001). Many marine
invertebrates, however, have ciliated
‘‘hair’’ cells that may be sensitive to
water movements, such as those caused
by currents or water particle motion
very close to a sound source
(Budelmann, 2010; Mackie and Singla,
2003). These cilia may allow
invertebrates to sense nearby prey or
predators or help with local navigation.
Marine invertebrates may produce and
use sound in territorial behavior, to
deter predators, to find a mate, and to
pursue courtship (Popper et al., 2001).
Both behavioral and auditory
brainstem response studies suggest that
crustaceans may sense sounds up to
three kilohertz (kHz), but best
sensitivity is likely below 200 Hz
(Lovell et al., 2005; Lovell et al., 2006;
Goodall et al., 1990). Most cephalopods
(e.g., octopus and squid) likely sense
low-frequency sound below 1,000 Hz,
with best sensitivities at lower
frequencies (Budelmann, 2010; Mooney
et al., 2010; Packard et al., 1990). A few
cephalopods may sense higher
frequencies up to 1,500 Hz (Hu et al.,
2009). Squid did not respond to toothed
whale ultrasonic echolocation clicks at
sound pressure levels ranging from 199
to 226 dB re 1 mPa peak-to-peak, likely
because these clicks were outside of
squid hearing range (Wilson et al.,
2007). However, squid exhibited alarm
responses when exposed to broadband
sound from an approaching seismic
airgun with received levels exceeding
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10001
145 to 150 dB re 1 mPa root mean square
(McCauley et al., 2000b).
Little information is available on the
potential impacts on marine
invertebrates of exposure to sonar,
explosions, and other sound-producing
activities. It is expected that most
marine invertebrates would not sense
mid- or high-frequency sounds, distant
sounds, or aircraft noise transmitted
through the air-water interface. Most
marine invertebrates would not be close
enough to intense sound sources, such
as some sonars, to potentially
experience impacts to sensory
structures. Any marine invertebrate
capable of sensing sound may alter its
behavior if exposed to non-impulsive
sound, although it is unknown if
responses to non-impulsive sounds
occur. Continuous noise, such as from
vessels, may contribute to masking of
relevant environmental sounds, such as
reef noise. Because the distance over
which most marine invertebrates are
expected to detect any sounds is limited
and vessels would be in transit, any
sound exposures with the potential to
cause masking or behavioral responses
would be brief and long-term impacts
are not expected. Although nonimpulsive underwater sounds produced
during training activities may briefly
impact individuals, intermittent
exposures to non-impulsive sounds are
not expected to impact survival, growth,
recruitment, or reproduction of
widespread marine invertebrate
populations.
Detonations associated with the
Navy’s GOA TMAA activities would
occur well offshore (the middle of the
GOA TMAA is 140 nm offshore; except
for a point near Cape Cleare on
Montague Island [12 nm away], the
nearest shoreline [Kenai Peninsula] is
24 nm north of the GOA TMAA
northern boundary). As water depth
increases away from shore, benthic
invertebrates would be less likely to be
impacted by detonations at or near the
surface. In addition, detonations near
the surface would release a portion of
their explosive energy into the air,
reducing the explosive impacts in the
water. Some marine invertebrates may
be sensitive to the low-frequency
component of impulsive sound, and
they may exhibit startle reactions or
temporary changes in swim speed in
response to an impulsive exposure.
Because exposures are brief, limited in
number, and spread over a large area, no
long-term impacts due to startle
reactions or short-term behavioral
changes are expected. Although
individual marine invertebrates may be
injured or killed during an explosion or
pile driving, no long-term impacts on
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the survival, growth, recruitment, or
reproduction of marine invertebrate
populations are expected.
Fish—Fish are not distributed
uniformly throughout the Study Area,
but are closely associated with a variety
of habitats. Some species range across
thousands of square miles while others
have small home ranges and restricted
distributions (Helfman et al., 2009). The
movements of some open-ocean species
may never overlap with coastal fishes
that spend their lives within several
hundred feet (a few hundred meters) of
the shore. Even within a single fish
species, the distribution and specific
habitats in which individuals occur may
be influenced by its developmental
stage, size, sex, reproductive condition,
and other factors.
The distribution and abundance of
fishes depends greatly on the physical
and biological factors of the marine
ecosystem, such as salinity,
temperature, dissolved oxygen,
population dynamics, predator and prey
interaction oscillations, seasonal
movements, reproduction and life
cycles, and recruitment success
(Helfman et al., 1997). A single factor is
rarely responsible for the distribution of
fish species; more often, a combination
of factors is accountable. For example,
open ocean species optimize their
growth, reproduction, and survival by
tracking gradients of temperature,
oxygen, or salinity (Helfman et al.,
1997). Another major component in
understanding species distribution is
the location of highly productive
regions, such as frontal zones. These
areas concentrate various prey species
and their predators, such as tuna, and
provide visual cues for the location of
target species for commercial fisheries
(NMFS, 2001).
At least 383 species belonging to 84
families of marine and anadromous
fishes have been reported from the
predominant ecosystems found in the
GOA TMAA. Detailed information on
taxa presence, distribution, and
characteristics are provided in Chapter
3 of the 2011 GOA FEIS/OEIS.
All fish have two sensory systems to
detect sound in the water: The inner ear,
which functions very much like the
inner ear in other vertebrates, and the
lateral line, which consists of a series of
receptors along the fish’s body (Popper,
2008). The inner ear generally detects
relatively higher-frequency sounds,
while the lateral line detects water
motion at low frequencies (below a few
hundred Hz) (Hastings and Popper,
2005a). Although hearing capability
data only exist for fewer than 100 of the
32,000 fish species, current data suggest
that most species of fish detect sounds
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from 50 to 1,000 Hz, with few fish
hearing sounds above 4 kHz (Popper,
2008). It is believed that most fish have
their best hearing sensitivity from 100 to
400 Hz (Popper, 2003b). Additionally,
some clupeids (shad in the subfamily
Alosinae) possess ultrasonic hearing
(i.e., able to detect sounds above
100,000 Hz) (Astrup, 1999). Permanent
hearing loss, or permanent threshold
shift has not been documented in fish.
The sensory hair cells of the inner ear
in fish can regenerate after they are
damaged, unlike in mammals where
sensory hair cells loss is permanent
(Lombarte et al., 1993; Smith et al.,
2006). As a consequence, any hearing
loss in fish may be as temporary as the
timeframe required to repair or replace
the sensory cells that were damaged or
destroyed (e.g., Smith et al., 2006).
Potential direct injuries from nonimpulsive sound sources, such as sonar,
are unlikely because of the relatively
lower peak pressures and slower rise
times than potentially injurious sources
such as explosives. Non-impulsive
sources also lack the strong shock waves
associated with an explosion. Therefore,
direct injury is not likely to occur from
exposure to non-impulsive sources such
as sonar, vessel noise, or subsonic
aircraft noise. Only a few fish species
are able to detect high-frequency sonar
and could have behavioral reactions or
experience auditory masking during
these activities. These effects are
expected to be transient and long-term
consequences for the population are not
expected. MFAS is unlikely to impact
fish species because most species are
unable to detect sounds in this
frequency range and vessels operating
MFAS would be transiting an area (not
stationary). While a large number of fish
species may be able to detect lowfrequency sonar and other active
acoustic sources, low-frequency active
usage is rare and mostly conducted in
deeper waters. Overall effects to fish
from non-impulsive sound sources
would be localized and infrequent.
Physical effects from pressure waves
generated by underwater sounds (e.g.
underwater explosions) could
potentially affect fish within proximity
of training activities. In particular, the
rapid oscillation between high- and lowpressure peaks has the potential to burst
the swim bladders and other gascontaining organs of fish (Keevin and
Hemen, 1997). Sublethal effects, such as
changes in behavior of fish, have been
observed in several occasions as a result
of noise produced by explosives
(National Research Council of the
National Academies, 2003; Wright,
1982). If an individual fish were
repeatedly exposed to sounds from
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underwater explosions that caused
alterations in natural behavioral
patterns or physiological stress, these
impacts could lead to long-term
consequences for the individual such as
reduced survival, growth, or
reproductive capacity. However, the
time scale of individual explosions is
very limited, and training exercises
involving explosions are dispersed in
space and time. Consequently, repeated
exposure of individual fish to sounds
from underwater explosions is not likely
and most acoustic effects are expected
to be short-term and localized. Longterm consequences for populations
would not be expected.
Marine Mammal Avoidance
Marine mammals may be temporarily
displaced from areas where Navy
training is occurring, but the area
should be utilized again after the
activities have ceased. Avoidance of an
area can help the animal avoid further
acoustic effects by avoiding or reducing
further exposure. The intermittent or
short duration of many activities should
prevent animals from being exposed to
stressors on a continuous basis (for the
GOA TMAA, training activities will not
occur continuously throughout the year,
but rather, for a maximum of 21 days
either once or twice annually). In areas
of repeated and frequent acoustic
disturbance, some animals may
habituate or learn to tolerate the new
baseline or fluctuations in noise level.
While some animals may not return to
an area, or may begin using an area
differently due to training activities,
most animals are expected to return to
their usual locations and behavior.
Other Expected Effects
Other sources that may affect marine
mammal habitat were considered in the
GOA DSEIS/OEIS and potentially
include the introduction of fuel, debris,
ordnance, and chemical residues into
the water column. The majority of highorder explosions would occur at or
above the surface of the ocean, and
would have no impacts on sediments
and minimal impacts on water quality.
While disturbance or strike from an item
falling through the water column is
possible, it is unlikely because (1)
objects sink slowly, (2) most projectiles
are fired at targets (and hit those
targets), and (3) animals are generally
widely dispersed throughout the water
column and over the Study Area.
Chemical, physical, or biological
changes in sediment or water quality
would not be detectable. In the event of
an ordnance failure, the energetic
materials it contained would remain
mostly intact. The explosive materials
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in failed ordnance items and metal
components from training would leach
slowly and would quickly disperse in
the water column. Chemicals from other
explosives would not be introduced into
the water column in large amounts and
all torpedoes would be recovered
following training activities, reducing
the potential for chemical
concentrations to reach levels that can
affect sediment quality, water quality, or
benthic habitats.
Preliminary Analysis and Negligible
Impact Determination
Negligible impact is ‘‘an impact
resulting from the specified activity that
cannot be reasonably expected to, and is
not reasonably likely to, adversely affect
the species or stock through effects on
annual rates of recruitment or survival’’
(50 CFR 216.103). A negligible impact
finding is based on the lack of likely
adverse effects on annual rates of
recruitment or survival (i.e., populationlevel effects). An estimate of the number
of takes, alone, is not enough
information on which to base an impact
determination, as the severity of
harassment may vary greatly depending
on the context and duration of the
behavioral response, many of which
would not be expected to have
deleterious impacts on the fitness of any
individuals. In determining whether the
expected takes will have a negligible
impact, in addition to considering
estimates of the number of marine
mammals that might be ‘‘taken,’’ NMFS
must consider other factors, such as the
likely nature of any responses (their
intensity, duration, etc.), the context of
any responses (critical reproductive
time or location, migration, etc.), as well
as the number and nature (e.g., severity)
of estimated Level A harassment takes,
the number of estimated mortalities, and
the status of the species. As a reminder,
the GOA TMAA training activities will
not occur continuously throughout the
year, but rather, for a maximum of 21
days either once or twice annually).
The Navy’s specified activities have
been described based on best estimates
of the maximum amount of sonar and
other acoustic source use or detonations
that the Navy would conduct. There
may be some flexibility in that the exact
number of hours, items, or detonations
may vary from year to year, but take
totals are not authorized to exceed the
5-year totals indicated in Tables 12–13.
We base our analysis and NID on the
maximum number of takes authorized,
although, as stated before, the number of
takes are only a part of the analysis,
which includes extensive qualitative
consideration of other contextual factors
that influence the degree of impact of
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the takes on the effected individuals. To
avoid repetition, we provide some
general analysis immediately below that
applies to all the species listed in Tables
13, given that some of the anticipated
effects (or lack thereof) of the Navy’s
training activities on marine mammals
are expected to be relatively similar in
nature. However, below that, we break
our analysis into species, or groups of
species where relevant similarities exist,
to provide more specific information
related to the anticipated effects on
individuals or where there is
information about the status or structure
of any species that would lead to a
differing assessment of the effects on the
population.
The Navy’s take request is based on
its model and post-model analysis. In
the discussions below, the ‘‘acoustic
analysis’’ refers to the Navy’s modeling
results and post-model analysis. The
model calculates sound energy
propagation from sonar, other active
acoustic sources, and explosives during
naval activities; the sound or impulse
received by animat dosimeters
representing marine mammals
distributed in the area around the
modeled activity; and whether the
sound or impulse received by a marine
mammal exceeds the thresholds for
effects. The model estimates are then
further analyzed to consider animal
avoidance and implementation of highly
effective mitigation measures to prevent
Level A harassment, resulting in final
estimates of effects due to Navy training
and testing. NMFS provided input to the
Navy on this process and the Navy’s
qualitative analysis is described in
detail in Chapter 6 of its LOA
application (https://www.nmfs.noaa.gov/
pr/permits/incidental/militry.htm).
Generally speaking, and especially
with other factors being equal, the Navy
and NMFS anticipate more severe
effects from takes resulting from
exposure to higher received levels
(though this is in no way a strictly linear
relationship throughout species,
individuals, or circumstances) and less
severe effects from takes resulting from
exposure to lower received levels. The
requested number of Level B takes does
not equate to the number of individual
animals the Navy expects to harass
(which is lower), but rather to the
instances of take (i.e., exposures above
the Level B harassment threshold) that
would occur. Additionally, these
instances may represent either a very
brief exposure (seconds) or, in some
cases, longer durations of exposure
within a day. Depending on the
location, duration, and frequency of
activities, along with the distribution
and movement of marine mammals,
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10003
individual animals may be exposed to
impulse or non-impulse sounds at or
above the Level B harassment threshold
on multiple days. However, the Navy is
currently unable to estimate the number
of individuals that may be taken during
training and testing activities. The
model results estimate the total number
of takes that may occur to a smaller
number of individuals. While the model
shows that an increased number of
exposures may take place due to an
increase in events/activities and
ordnance, the types and severity of
individual responses to training and
testing activities are not expected to
change.
Behavioral Harassment
As discussed previously in this
proposed rule, marine mammals can
respond to LF/MFAS/HFAS in many
different ways, a subset of which
qualifies as behavioral harassment. As
described in the proposed rule, the
Navy uses the behavioral response
function to quantify the number of
behavioral responses that would qualify
as Level B behavioral harassment under
the MMPA. As the statutory definition
is currently applied, a wide range of
behavioral reactions may qualify as
Level B harassment under the MMPA,
including but not limited to avoidance
of the sound source, temporary changes
in vocalizations or dive patterns,
temporary avoidance of an area, or
temporary disruption of feeding,
migrating, or reproductive behaviors.
Some of the lower level physiological
stress responses discussed earlier would
also likely co-occur with the predicted
harassments, although these responses
are more difficult to detect and fewer
data exist relating these responses to
specific received levels of sound. Level
B takes, then, may have a stress-related
physiological component as well;
however, we would not expect the
Navy’s generally short-term,
intermittent, and (in the case of sonar)
transitory activities to create conditions
of long-term, continuous noise leading
to long-term physiological stress
responses in marine mammals.
The estimates calculated using the
behavioral response function do not
differentiate between the different types
of potential reactions. Nor do the
estimates provide information regarding
the potential fitness or other biological
consequences of the reactions on the
affected individuals. We therefore
consider the available scientific
evidence to determine the likely nature
of the modeled behavioral responses
and the potential fitness consequences
for affected individuals.
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For LF/MFAS/HFAS use in the GOA
TMAA, the Navy provided information
(Table 14) estimating the percentage of
behavioral harassment that would occur
within the 6–dB bins (without
considering mitigation or avoidance). As
mentioned above, an animal’s exposure
to a higher received level is more likely
to result in a behavioral response that is
more likely to adversely affect the
health of the animal. As illustrated
below, the majority (including about 72
percent for the most powerful ASW
hull-mounted sonar, which is
responsible for a large portion of the
sonar takes) of calculated takes from
MFAS result from exposures less than
156 dB. Less than 1 percent of the takes
are expected to result from exposures
above 174 dB. Specifically, given a
range of behavioral responses that may
be classified as Level B harassment, to
the degree that higher received levels
are expected to result in more severe
behavioral responses, only a small
percentage of the anticipated Level B
harassment from Navy activities might
necessarily be expected to potentially
result in more severe responses,
especially when the distance from the
source at which the levels below are
received is considered (see Table 14).
Marine mammals are able to discern the
distance of a given sound source, and
given other equal factors (including
received level), they have been reported
to respond more to sounds that are
closer (DeRuiter et al., 2013). Further,
the estimated number of responses do
not reflect either the duration or context
of those anticipated responses, some of
which will be of very short duration,
and other factors should be considered
when predicting how the estimated
takes may affect individual fitness. A
recent study by Moore and Barlow
(2013) emphasizes the importance of
context (e.g., behavioral state of the
animals, distance from the sound
source, etc.) in evaluating behavioral
responses of marine mammals to
acoustic sources.
TABLE 14—NON-IMPULSIVE RANGES IN 6-dB BINS AND PERCENTAGE OF BEHAVIORAL HARASSMENTS
Sonar bin MF1 (e.g., SQS–53;
ASW hull
mounted sonar)
Received level
Distance at which
levels occur
within radius
of source
(m)
Percentage of
behavioral
harassments
occurring at
given levels
Sonar bin MF4 (e.g., AQS–22;
ASW dipping
sonar)
Distance at which
levels occur
within radius
of source
(m)
Sonar Bin MF5
(e.g., SSQ–62;
ASW sonobuoy)
Percentage of
behavioral
harassments
occurring at
given levels
Distance at which
levels occur
within radius
of source
(m)
Percentage of
behavioral
harassments
occurring at
given levels
Low Frequency Cetaceans
120
126
132
138
144
150
156
162
168
174
180
186
192
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
<126
<132
<138
<144
<150
<156
<162
<168
<174
<180
<186
<192
<198
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
178,750–156,450
156,450–147,500
147,500–103,700
103,700–97,950
97,950–55,050
55,050–49,900
49,900–10,700
10,700–4,200
4,200–1,850
1,850–850
850–400
400–200
200–100
0.00
0.00
0.21
0.33
13.73
5.28
72.62
6.13
1.32
0.30
0.07
0.01
0.00
100,000–92,200
92,200–55,050
55,050–46,550
46,550–15,150
15,150–5,900
5,900–2,700
2,700–1,500
1,500–200
200–100
100–<50
<50
<50
<50
0.00
0.11
1.08
35.69
26.40
17.43
9.99
9.07
0.18
0.05
0.00
0.00
0.00
22,800–15,650
15,650–11,850
11,850–6,950
6,950–3,600
3,600–1,700
1,700–250
250–100
100–<50
<50
<50
<50
<50
<50
0.00
0.05
2.84
16.04
33.63
44.12
2.56
0.76
0.00
0.00
0.00
0.00
0.00
0.00
0.11
1.08
35.69
26.40
17.43
9.99
9.07
0.18
0.05
0.00
0.00
0.00
23,413–16,125
16,125–11,500
11,500–6,738
6,738–3,825
3,825–1,713
1,713–250
250–150
150–<50
<50
<50
<50
<50
<50
0.00
0.06
2.56
13.35
37.37
42.85
1.87
1.93
0.00
0.00
0.00
0.00
0.00
Mid Frequency Cetaceans
120
126
132
138
144
150
156
162
168
174
180
186
192
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
≤
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
SPL
<126
<132
<138
<144
<150
<156
<162
<168
<174
<180
<186
<192
<198
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
179,400–156,450
156,450–147,500
147,500–103,750
103,750–97,950
97,950–55,900
55,900–49,900
49,900–11,450
11,450–4,350
4,350–1,850
1,850–850
850–400
400–200
200–100
0.00
0.00
0.21
0.33
13.36
6.12
71.18
7.01
1.42
0.29
0.07
0.01
0.00
100,000–92,200
92,200–55,050
55,050–46,550
46,550–15,150
15,150–5,900
5,900–2,700
2,700–1,500
1,500–200
200–100
100–<50
<50
<50
<50
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Notes: (1) ASW = anti-submarine warfare, m = meters, SPL = sound pressure level; (2) Odontocete behavioral response function is also used for high-frequency
cetaceans, phocid seals, otariid seals and sea lions, and sea otters.
Although the Navy has been
monitoring to discern the effects of LF/
MFAS/HFAS on marine mammals since
2006, and research on the effects of
MFAS is advancing, our understanding
of exactly how marine mammals in the
Study Area will respond to LF/MFAS/
HFAS is still improving. The Navy has
submitted more than 80 reports,
including Major Exercise Reports,
Annual Exercise Reports, and
Monitoring Reports, documenting
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hundreds of thousands of marine
mammals across Navy range complexes,
and there are only two instances of overt
behavioral disturbances that have been
observed. One cannot conclude from
these results that marine mammals were
not harassed from MFAS/HFAS, as a
portion of animals within the area of
concern were not seen (especially those
more cryptic, deep-diving species, such
as beaked whales or Kogia spp.), the full
series of behaviors that would more
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accurately show an important change is
not typically seen (i.e., only the surface
behaviors are observed), and some of the
non-biologist watchstanders might not
be well-qualified to characterize
behaviors. However, one can say that
the animals that were observed did not
respond in any of the obviously more
severe ways, such as panic, aggression,
or anti-predator response.
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Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Proposed Rules
Diel Cycle
As noted previously, many animals
perform vital functions, such as feeding,
resting, traveling, and socializing on a
diel cycle (24-hour cycle). Behavioral
reactions to noise exposure (when
taking place in a biologically important
context, such as disruption of critical
life functions, displacement, or
avoidance of important habitat) are
more likely to be significant if they last
more than one diel cycle or recur on
subsequent days (Southall et al., 2007).
Consequently, a behavioral response
lasting less than one day and not
recurring on subsequent days is not
considered severe unless it could
directly affect reproduction or survival
(Southall et al., 2007). Note that there is
a difference between multiple-day
substantive behavioral reactions and
multiple-day anthropogenic activities.
For example, just because an at-sea
exercise lasts for multiple days does not
necessarily mean that individual
animals are either exposed to those
exercises for multiple days or, further,
exposed in a manner resulting in a
sustained multiple day substantive
behavioral response. Large multi-day
Navy exercises, such as those proposed
in the GOA TMAA, typically include
vessels that are continuously moving at
speeds typically 10–15 knots, or higher,
and likely cover large areas that are
relatively far from shore, in addition to
the fact that marine mammals are
moving as well, which would make it
unlikely that the same animal could
remain in the immediate vicinity of the
ship for the entire duration of the
exercise. Additionally, the Navy does
not necessarily operate active sonar the
entire time during an exercise. While it
is certainly possible that these sorts of
exercises could overlap with individual
marine mammals multiple days in a row
at levels above those anticipated to
result in a take, because of the factors
mentioned above, it is considered
unlikely for the majority of takes. It does
not mean that a behavioral response is
necessarily sustained for multiple days,
but instead necessitates the
consideration of likely duration and
context to assess any effects on the
individual’s fitness.
Durations for non-impulsive activities
utilizing tactical sonar sources vary and
are fully described in Appendix A of the
GOA DSEIS/OEIS. ASW training
exercises using MFAS/HFAS proposed
for the GOA TMAA generally last for 2–
16 hours, and may have intervals of
non-activity in between. Because of the
need to train in a large variety of
situations (in the case of the GOA
TMAA, complex bathymetric and
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oceanographic conditions include a
continental shelf, submarine canyons,
seamounts, and fresh water infusions
from multiple sources), the Navy does
not typically conduct successive ASW
exercises in the same locations. Given
the average length of ASW exercises
(times of continuous sonar use) and
typical vessel speed, combined with the
fact that the majority of the cetaceans in
the GOA TMAA Study Area would not
likely remain in an area for successive
days, it is unlikely that an animal would
be exposed to MFAS/HFAS at levels
likely to result in a substantive response
that would then be carried on for more
than one day or on successive days.
With the exception of SINKEXs, the
planned explosive exercises for the
GOA TMAA are of a short duration (1–
6 hours). Although explosive exercises
may sometimes be conducted in the
same general areas repeatedly, because
of their short duration and the fact that
they are in the open ocean and animals
can easily move away, it is similarly
unlikely that animals would be exposed
for long, continuous amounts of time.
Although SINKEXs may last for up to 48
hrs, only two are planned annually for
the GOA TMAA training activities, they
are stationary and conducted in deep,
open water (where fewer marine
mammals would typically be expected
to be randomly encountered), and they
have a rigorous monitoring and
shutdown procedures, all of which
make it unlikely that individuals would
be exposed to the exercise for extended
periods or on consecutive days.
TTS
As mentioned previously, TTS can
last from a few minutes to days, be of
varying degree, and occur across various
frequency bandwidths, all of which
determine the severity of the impacts on
the affected individual, which can range
from minor to more severe. The TTS
sustained by an animal is primarily
classified by three characteristics:
1. Frequency—Available data (of midfrequency hearing specialists exposed to
mid- or high-frequency sounds; Southall
et al., 2007) suggest that most TTS
occurs in the frequency range of the
source up to one octave higher than the
source (with the maximum TTS at 1⁄2
octave above). The more powerful MF
sources used have center frequencies
between 3.5 and 8 kHz and the other
unidentified MF sources are, by
definition, less than 10 kHz, which
suggests that TTS induced by any of
these MF sources would be in a
frequency band somewhere between
approximately 2 and 20 kHz. There are
fewer hours of HF source use and the
sounds would attenuate more quickly,
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10005
plus they have lower source levels, but
if an animal were to incur TTS from
these sources, it would cover a higher
frequency range (sources are between 20
and 100 kHz, which means that TTS
could range up to 200 kHz; however, HF
systems are typically used less
frequently and for shorter time periods
than surface ship and aircraft MF
systems, so TTS from these sources is
even less likely). TTS from explosives
would be broadband. Vocalization data
for each species, which would inform
how TTS might specifically interfere
with communications with conspecifics,
was provided in the LOA application.
2. Degree of the shift (i.e., by how
many dB the sensitivity of the hearing
is reduced)—Generally, both the degree
of TTS and the duration of TTS will be
greater if the marine mammal is exposed
to a higher level of energy (which would
occur when the peak dB level is higher
or the duration is longer). The threshold
for the onset of TTS was discussed
previously in this proposed rule. An
animal would have to approach closer
to the source or remain in the vicinity
of the sound source appreciably longer
to increase the received SEL, which
would be difficult considering the
Lookouts and the nominal speed of an
active sonar vessel (10–15 knots). In the
TTS studies (see Threshold Shift
section), some using exposures of
almost an hour in duration or up to 217
SEL, most of the TTS induced was 15
dB or less, though Finneran et al. (2007)
induced 43 dB of TTS with a 64-second
exposure to a 20 kHz source. However,
MFAS emits a ping typically every 50
seconds, and incurring those levels of
TTS is highly unlikely.
3. Duration of TTS (recovery time)—
In the TTS laboratory studies (see
Threshold Shift section), some using
exposures of almost an hour in duration
or up to 217 SEL, almost all individuals
recovered within 1 day (or less, often in
minutes), although in one study
(Finneran et al., 2007), recovery took 4
days.
Based on the range of degree and
duration of TTS reportedly induced by
exposures to non-pulse sounds of
energy higher than that to which freeswimming marine mammals in the field
are likely to be exposed during MFAS/
HFAS training exercises in the GOA
TMAA, it is unlikely that marine
mammals would ever sustain a TTS
from MFAS that alters their sensitivity
by more than 20 dB for more than a few
days (and any incident of TTS would
likely be far less severe due to the short
duration of the majority of the exercises
and the speed of a typical vessel). Also,
for the same reasons discussed in the
Diel Cycle section, and because of the
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short distance within which animals
would need to approach the sound
source, it is unlikely that animals would
be exposed to the levels necessary to
induce TTS in subsequent time periods
such that their recovery is impeded.
Additionally, though the frequency
range of TTS that marine mammals
might sustain would overlap with some
of the frequency ranges of their
vocalization types, the frequency range
of TTS from MFAS (the source from
which TTS would most likely be
sustained because the higher source
level and slower attenuation make it
more likely that an animal would be
exposed to a higher received level)
would not usually span the entire
frequency range of one vocalization
type, much less span all types of
vocalizations or other critical auditory
cues. If impaired, marine mammals
would typically be aware of their
impairment and are sometimes able to
implement behaviors to compensate (see
Acoustic Masking or Communication
Impairment section), though these
compensations may incur energetic
costs.
Acoustic Masking or Communication
Impairment
Masking only occurs during the time
of the signal (and potential secondary
arrivals of indirect rays), versus TTS,
which continues beyond the duration of
the signal. Standard MFAS typically
pings every 50 seconds for hullmounted sources. For the sources for
which we know the pulse length, most
are significantly shorter than hullmounted active sonar, on the order of
several microseconds to tens of
microseconds. For hull-mounted active
sonar, though some of the vocalizations
that marine mammals make are less
than one second long, there is only a 1
in 50 chance that they would occur
exactly when the ping was received, and
when vocalizations are longer than one
second, only parts of them are masked.
Alternately, when the pulses are only
several microseconds long, the majority
of most animals’ vocalizations would
not be masked. Masking effects from
MFAS/HFAS are expected to be
minimal. If masking or communication
impairment were to occur briefly, it
would be in the frequency range of
MFAS, which overlaps with some
marine mammal vocalizations; however,
it would likely not mask the entirety of
any particular vocalization,
communication series, or other critical
auditory cue, because the signal length,
frequency, and duty cycle of the MFAS/
HFAS signal does not perfectly mimic
the characteristics of any marine
mammal’s vocalizations. The other
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sources used in Navy training and
testing, many of either higher
frequencies (meaning that the sounds
generated attenuate even closer to the
source) or lower amounts of operation,
are similarly not expected to result in
masking.
PTS, Injury, or Mortality
NMFS believes that many marine
mammals would deliberately avoid
exposing themselves to the received
levels of active sonar necessary to
induce injury by moving away from or
at least modifying their path to avoid a
close approach. Additionally, in the
unlikely event that an animal
approaches the sonar vessel at a close
distance, NMFS believes that the
mitigation measures (i.e., shutdown/
powerdown zones for MFAS/HFAS)
would typically ensure that animals
would not be exposed to injurious levels
of sound. As discussed previously, the
Navy utilizes both aerial (when
available) and passive acoustic
monitoring (during all ASW exercises)
in addition to watchstanders on vessels
to detect marine mammals for
mitigation implementation.
If a marine mammal is able to
approach a surface vessel within the
distance necessary to incur PTS, the
likely speed of the vessel (nominal 10–
15 knots) would make it very difficult
for the animal to remain in range long
enough to accumulate enough energy to
result in more than a mild case of PTS.
As mentioned previously and in relation
to TTS, the likely consequences to the
health of an individual that incurs PTS
can range from mild to more serious
dependent upon the degree of PTS and
the frequency band it is in, and many
animals are able to compensate for the
shift, although it may include energetic
costs. Only 5 Level A (PTS) takes per
year are predicted from GOA training
activities, and these are all Dall’s
porpoise—not large whale species or
beaked whales. We also assume that the
acoustic exposures sufficient to trigger
onset PTS (or TTS) would be
accompanied by physiological stress
responses, although the sound
characteristics that correlate with
specific stress responses in marine
mammals are poorly understood. As
discussed above for Behavioral
Harassment, we would not expect the
Navy’s generally short-term,
intermittent, and (in the case of sonar)
transitory activities to create conditions
of long-term, continuous noise leading
to long-term physiological stress
responses in marine mammals. No other
injurious takes or mortality are
predicted. As discussed previously,
marine mammals (especially beaked
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whales) could potentially respond to
MFAS at a received level lower than the
injury threshold in a manner that
indirectly results in the animals
stranding. The exact mechanism of this
potential response, behavioral or
physiological, is not known. When
naval exercises have been associated
with strandings in the past, it has
typically been when three or more
vessels are operating simultaneously, in
the presence of a strong surface duct,
and in areas of constricted channels,
semi-enclosed areas, and/or steep
bathymetry. While these features
certainly do not define the only factors
that can contribute to a stranding, and
while they need not all be present in
their aggregate to increase the likelihood
of a stranding, it is worth noting that
they are not all present in the GOA
TMAA, which only has a strong surface
duct present during the winter, and
does not have bathymetry or constricted
channels of the type that have been
present in the sonar associated
strandings. When this is combined with
consideration of the number of hours of
active sonar training that will be
conducted and the total duration of all
training exercises (a maximum of 21
days once or twice a year), we believe
that the probability is small that this
will occur. Lastly, an active sonar
shutdown protocol for strandings
involving live animals milling in the
water minimizes the chances that these
types of events turn into mortalities.
As stated previously, there have been
no recorded Navy vessel strikes of any
marine mammals during training in the
GOA Study Area to date, nor were takes
by injury or mortality resulting from
vessel strike predicted in the Navy’s
analysis.
Group and Species-Specific Analysis
Predicted effects on marine mammals
from exposures to sonar and other active
acoustic sources and explosions during
annual training activities are shown in
Table 13. The vast majority of predicted
exposures (greater than 99 percent) are
expected to be Level B harassment (noninjurious TTS and behavioral reactions)
from sonar and other active acoustic
sources at relatively low received levels
(Table 14). The acoustic analysis
predicts the majority of marine mammal
species in the Study Area would not be
exposed to explosive (impulsive)
sources associated with training
activities. Only Dall’s porpoise is
predicted to have Level B (TTS)
exposures resulting from explosives,
and only a limited number (5) of Dall’s
porpoise are expected to have injurious
take (PTS) resulting from sonar and
other active acoustic sources and
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explosions. There are no lethal takes
predicted for any marine mammal
species for the GOA activities.
The analysis below may in some cases
(e.g., mysticetes, porpoises, pinnipeds)
address species collectively if they
occupy the same functional hearing
group (i.e., low-, mid-, and highfrequency cetaceans and pinnipeds in
water), have similar hearing capabilities,
and/or are known to generally
behaviorally respond similarly to
acoustic stressors. Where there are
meaningful differences between species
or stocks in anticipated individual
responses to activities, impact of
expected take on the population due to
differences in population status, or
impacts on habitat, they will either be
described within the section or the
species will be included as a separate
sub-section.
Mysticetes—The Navy’s acoustic
analysis predicts that 2,923 instances of
Level B harassmant of mysticete whales
may occur in the Study Area each year
from sonar and other active acoustic
sources during training activities.
Annual species-specific take estimates
are as follows: 7 North Pacific right
whales (Eastern North Pacific stock),
139 humpback whales (Central North
Pacific and Western North Pacific
stocks), 95 blue whales (Eastern North
Pacific stock), 2,582 fin whales
(Northeast Pacific stock), 13 sei whales
(Eastern North Pacific stock), and 87
minke whales (Alaska stock). Of these
species, humpback, blue, fin, sei, and
North Pacific right whales are listed as
endangered under the ESA and depleted
under the MMPA. NMFS is currently
engaged in an internal Section 7
consultation under the ESA and the
outcome of that consultation will
further inform our final decision. Based
on the distribution information
presented in the LOA application, it is
highly unlikely that gray whales would
be encountered in the Study Area
during events involving use of sonar
and other active acoustic sources. The
acoustic analysis did not predict any
takes of gray whales and NMFS is not
authorizing any takes of this species.
Generally, these represent a limited
number of takes relative to population
estimates for most mysticete stocks in
the Study Area (Table 6). When the
numbers of behavioral takes are
compared to the estimated stock
abundance and if one assumes that each
take happens to a separate animal, less
than approximately 20 percent of each
of these stocks (with the exception of
the Northeast Pacific stock of fin whale
and the Alaska stock of minke whale for
which there currently are no reliable
population estimates because only
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portions of the stocks’ range have been
surveyed [Muto and Angliss, 2015])
would be behaviorally harassed during
the course of a year. Because the
estimates given above represent the total
number of exposures and not
necessarily the number of individuals
exposed, it is more likely that fewer
individuals would be taken, but a subset
would be taken more than one time per
year. In the ocean, the use of sonar and
other active acoustic sources is transient
and is unlikely to repeatedly expose the
same population of animals over a short
period.
Level B harassment takes are
anticipated to be in the form of TTS and
behavioral reactions and no injurious
takes of North Pacific right, humpback,
blue, fin, minke, or sei whales from
sonar and other active acoustic stressors
or explosives are expected. The majority
of acoustic effects to mysticetes from
sonar and other active sound sources
during training activities would be
primarily from anti-submarine warfare
events involving surface ships and hull
mounted sonar. Research and
observations show that if mysticetes are
exposed to sonar or other active acoustic
sources they may react in a number of
ways depending on the characteristics
of the sound source, their experience
with the sound source, and whether
they are migrating or on seasonal
grounds (i.e., breeding or feeding).
Reactions may include alerting,
breaking off feeding dives and surfacing,
diving or swimming away, or no
response at all (Richardson, 1995;
Nowacek, 2007; Southall et al., 2007;
Finneran and Jenkins, 2012).
Richardson et al. (1995) noted that
avoidance (temporary displacement of
an individual from an area) reactions are
the most obvious manifestations of
disturbance in marine mammals.
Avoidance is qualitatively different
from the startle or flight response, but
also differs in the magnitude of the
response (i.e., directed movement, rate
of travel, etc.). Oftentimes avoidance is
temporary, and animals return to the
area once the noise has ceased.
Additionally, migrating animals may
ignore a sound source, or divert around
the source if it is in their path.
Specific to U.S. Navy systems using
low frequency sound, studies were
undertaken in 1997–98 pursuant to the
Navy’s Low Frequency Sound Scientific
Research Program. These studies found
only short-term responses to low
frequency sound by mysticetes (fin,
blue, and humpback whales) including
changes in vocal activity and avoidance
of the source vessel (Clark, 2001; Miller
et al., 2000; Croll et al., 2001; Fristrup
et al., 2003; Nowacek et al., 2007).
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Baleen whales exposed to moderate
low-frequency signals demonstrated no
variation in foraging activity (Croll et
al., 2001). Low-frequency signals of the
Acoustic Thermometry of Ocean
Climate sound source were not found to
affect dive times of humpback whales in
Hawaiian waters (Frankel and Clark,
2000).
Specific to mid-frequency sound,
´
studies by Melcon et al. (2012) in the
Southern California Bight found that the
likelihood of blue whale low-frequency
calling (usually associated with feeding
behavior) decreased with an increased
level of MFAS, beginning at a SPL of
approximately 110–120 dB re 1 mPa.
However, it is not known whether the
lower rates of calling actually indicated
a reduction in feeding behavior or social
contact since the study used data from
remotely deployed, passive acoustic
monitoring buoys. Results from the
2010–2011 field season of an ongoing
behavioral response study in Southern
California waters indicated that in some
cases and at low received levels, tagged
blue whales responded to MFAS but
that those responses were mild and
there was a quick return to their
baseline activity (Southall et al., 2011;
Southall et al., 2012b). Blue whales
responded to a mid-frequency sound
source, with a source level between 160
and 210 dB re 1 mPa at 1 m and a
received sound level up to 160 dB re 1
mPa, by exhibiting generalized
avoidance responses and changes to
dive behavior during the exposure
experiments (CEE) (Goldbogen et al.,
2013). However, reactions were not
consistent across individuals based on
received sound levels alone, and likely
were the result of a complex interaction
between sound exposure factors such as
proximity to sound source and sound
type (MFAS simulation vs. pseudorandom noise), environmental
conditions, and behavioral state. Surface
feeding whales did not show a change
in behavior during CEEs, but deep
feeding and non-feeding whales showed
temporary reactions that quickly abated
after sound exposure. Distances of the
sound source from the whales during
CEEs were sometimes less than a mile.
Blue whales have been documented
exhibiting a range of foraging strategies
for maximizing feeding dependent on
the density of their prey at a given
location (Goldbogen et al., 2015), so it
may be that a temporary behavioral
reaction or avoidance of a location
where feeding was occurring is not
meaningful to the life history of an
animal. The preliminary findings from
´
Goldbogen et al. (2013) and Melcon et
al. (2012) are generally consistent with
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the Navy’s criteria and thresholds for
predicting behavioral effects to
mysticetes from sonar and other active
acoustic sources used in the quantitative
acoustic effects analysis for GOA. The
Navy’s behavioral response function
predicts the probability of a behavioral
response that rises to a Level B take for
individuals exposed to a received SPL
of 120 dB re 1 mPa or greater, with an
increasing probability of reaction with
increased received level as
´
demonstrated in Melcon et al. (2012).
High-frequency systems are notably
outside of mysticetes’ ideal hearing and
vocalization range and it is unlikely that
they would cause a significant
behavioral reaction.
Most Level B harassments to
mysticetes from sonar in the Study Area
would result from received levels less
than 156 dB SPL. Therefore, the
majority of Level B takes are expected
to be in the form of milder responses
(i.e., lower-level exposures that still rise
to the level of take, but would likely be
less severe in the range of responses that
qualify as take) of a generally short
duration. As mentioned earlier in this
section, we anticipate more severe
effects from takes when animals are
exposed to higher received levels. Most
low-frequency (mysticetes) cetaceans
observed in studies usually avoided
sound sources at levels of less than or
equal to 160 dB re 1mPa. Occasional
milder behavioral reactions are unlikely
to cause long-term consequences for
individual animals or populations. Even
if sound exposure were to be
concentrated in a relatively small
geographic area over a long period of
time (e.g., days or weeks during major
training exercises), we would expect
that some individual whales would
avoid areas where exposures to acoustic
stressors are at higher levels. For
example, Goldbogen et al. (2013)
indicated some horizontal displacement
of deep foraging blue whales in
response to simulated MFA sonar.
Given these animal’s mobility and large
ranges, we would expect these
individuals to temporarily select
alternative foraging sites nearby until
the exposure levels in their initially
selected foraging area have decreased.
Therefore, even temporary displacement
from initially selected foraging habitat is
not expected to impact the fitness of any
individual animals because we would
expect equivalent foraging to be
available in close proximity. Because we
do not expect any fitness consequences
from any individual animals, we do not
expect any population level effects from
these behavioral responses.
As explained above, recovery from a
threshold shift (TTS) can take a few
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minutes to a few days, depending on the
exposure duration, sound exposure
level, and the magnitude of the initial
shift, with larger threshold shifts and
longer exposure durations requiring
longer recovery times (Finneran et al.,
2005; Finneran and Schlundt, 2010;
Mooney et al., 2009a; Mooney et al.,
2009b). However, large threshold shifts
are not anticipated for these activities
because of the unlikelihood that animals
will remain within the ensonified area
(due to the short duration of the
majority of exercises, the speed of the
vessels, and the short distance within
which the animal would need to
approach the sound source) at high
levels for the duration necessary to
induce larger threshold shifts.
Threshold shifts do not necessarily
affect all hearing frequencies equally, so
some threshold shifts may not interfere
with an animal’s hearing of biologically
relevant sounds. Furthermore, the
implementation of mitigation and the
sightability of mysticetes (due to their
large size) reduces the potential for a
significant behavioral reaction or a
threshold shift to occur.
Overall, the number of predicted
behavioral reactions is low and
occasional behavioral reactions are
unlikely to cause long-term
consequences for individual animals or
populations. This assessment of longterm consequences is based in part on
findings from ocean areas where the
Navy has been intensively training and
testing with sonar and other active
acoustic sources for decades. While
there are many factors such as the end
of large-scale commercial whaling
complicating any analysis, there is no
data suggesting any long-term
consequences to mysticetes from
exposure to sonar and other active
acoustic sources. On the contrary, there
are findings suggesting mysticete
populations are increasing in the two
primary locations (Southern California
and Hawaii) where the Navy’s most
intensively used range complexes are
located. These findings include: (1)
Calambokidis et al. (2009b) indicating a
significant upward trend in abundance
of for blue whales in Southern
California; (2) the recovery of gray
whales that migrate through the Navy’s
SOCAL Range Complex twice a year; (3)
work by Moore and Barlow (2011)
indicating evidence of increasing fin
whale abundance in the California
Current area, which includes the
SOCAL Range Complex; (4) the range
expansion and increasing presence of
Bryde’s whales south of Point
Conception in Southern California
(Kerosky et al. 2012); and (5) the ocean
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area contained within the Hawaii Range
Complex continuing to function as a
critical breeding, calving, and nursing
area to the point at which the overall
humpback whale population in the
North Pacific is now greater than some
prior estimates of pre-whaling
abundance (Barlow et al., 2011). The
implementation of mitigation and the
sightability of mysticetes (due to their
large size) reduces the potential for a
significant behavioral reaction or a
threshold shift to occur. Furthermore,
there is no designated critical habitat for
mysticetes in the Study Area. As
discussed in the Consideration of Time/
Area Limitations section of this rule,
review of the NMFS-identified feeding
and migration areas showed there is
only minimal (<1 percent) spatial
overlap with the GOA TMAA and the
North Pacific right whale feeding area
southeast of Kodiak Island and minimal
(<1 percent) spatial overlap with a small
portion of the gray whale migration area
offshore of Kenai Peninsula (Ferguson et
al., 2015b). Those areas of overlap at the
corners of the GOA TMAA are very
unlikely to have any Navy training
activity. Further, the grey whale
migration area is only applicable in the
early spring and late fall, while training
activities are proposed for May to
October (with June/July the main
months of training, historically).
Therefore, it is very unlikely there
would be an effect to feeding or
migrating activities if right whales or
gray whales were present. Additionally,
appropriate mitigation measures (as
detailed in the Mitigation section above)
would be implemented for any detected
marine mammals and thus further
reducing the potential for the feeding or
migration activities to be affected. The
Navy proposes to monitor use of active
sonar within the North Pacific right
whale feeding area and gray whale
migration areas, to the extent that active
sonar training does occur in these areas,
and to report that use to NMFS in
classified annual reports (see Proposed
Reporting) to inform future adaptive
management of activities within the
GOA TMAA.
Consequently, the GOA TMAA
activities are not expected to adversely
impact rates of recruitment or survival
of mysticete whales.
Sperm Whales—The Navy’s acoustic
analysis indicates that 197 instances of
Level B harassment of sperm whales
(North Pacific stock; currently there are
no reliable abundance estimates for this
stock [Muto and Angliss, 2015]) may
occur in the Study Area each year from
sonar or other active acoustic stressors
during training activities. Sperm whales
are listed as endangered under the ESA
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and depleted under the MMPA. NMFS
is currently engaged in an internal
Section 7 consultation under the ESA
and the outcome of that consultation
will further inform our final decision.
These Level B takes are anticipated to be
in the form of TTS and behavioral
reactions and no injurious takes of
sperm whales from sonar and other
active acoustic stressors or explosives
are requested or proposed for
authorization. Sperm whales have
shown resilience to acoustic and human
disturbance, although they may react to
sound sources and activities within a
few kilometers. Sperm whales that are
exposed to activities that involve the
use of sonar and other active acoustic
sources may alert, ignore the stimulus,
avoid the area by swimming away or
diving, or display aggressive behavior
(Richardson, 1995; Nowacek, 2007;
Southall et al., 2007; Finneran and
Jenkins, 2012). Some (but not all) sperm
whale vocalizations might overlap with
the MFAS/HFAS TTS frequency range,
which could temporarily decrease an
animal’s sensitivity to the calls of
conspecifics or returning echolocation
signals. However, as noted previously,
NMFS does not anticipate TTS of a long
duration or severe degree to occur as a
result of exposure to MFAS/HFAS.
Recovery from a threshold shift (TTS)
can take a few minutes to a few days,
depending on the exposure duration,
sound exposure level, and the
magnitude of the initial shift, with
larger threshold shifts and longer
exposure durations requiring longer
recovery times (Finneran et al., 2005;
Mooney et al., 2009a; Mooney et al.,
2009b; Finneran and Schlundt, 2010).
Large threshold shifts are not
anticipated for these activities because
of the unlikelihood that animals will
remain within the ensonified area (due
to the short duration of the majority of
exercises, the speed of the vessels, and
the short distance within which the
animal would need to approach the
sound source) at high levels for the
duration necessary to induce larger
threshold shifts. Threshold shifts do not
necessarily affect all hearing frequencies
equally, so some threshold shifts may
not interfere with an animal’s hearing of
biologically relevant sounds. No sperm
whales are predicted to be exposed to
MFAS/HFAS sound levels associated
with PTS or injury.
The majority of Level B takes are
expected to be in the form of mild
responses (low-level exposures) and of a
generally short duration. Relative to the
population size, this activity is
anticipated to result only in a limited
number of Level B harassment takes.
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Because the estimates given above
represent the total number of exposures
and not necessarily the number of
individuals exposed, it is more likely
that fewer individuals would be taken,
but a subset would be taken more than
one time per year. In the ocean, the use
of sonar and other active acoustic
sources is transient and is unlikely to
repeatedly expose the same population
of animals over a short period. Overall,
the number of predicted behavioral
reactions are unlikely to cause long-term
consequences for individual animals or
populations. The GOA activities are not
expected to occur in an area/time of
specific importance for reproductive,
feeding, or other known critical
behaviors for sperm whales, and there is
no designated critical habitat in the
Study Area. Consequently, the activities
are not expected to adversely impact
annual rates of recruitment or survival
of sperm whales.
Dolphins and Small Whales—The
Navy’s acoustic analysis predicts the
following instances of Level B
harassment of delphinids (dolphins and
small whales) each year from sonar and
other active acoustic sources associated
with training activities in the Study
Area: 762 killer whales (Alaska
Resident; Eastern North Pacific
Offshore; AT1 Transient; and GOA,
Aleutian Island, and Bearing Sea
Transient stocks) and 1,963 Pacific
white-sided dolphins (North Pacific
stock). These represent a limited
number of takes relative to population
estimates for delphinid stocks in the
Study Area (Table 6). When the
numbers of behavioral takes are
compared to the estimated stock
abundance and if one assumes that each
take happens to a separate animal, less
than 25 percent of each of the killer
whale stocks and less than 8 percent of
the North Pacific stock of Pacific whitesided dolphin would be behaviorally
harassed during the course of a year.
More likely, slightly fewer individuals
would be harassed, but a subset would
be harassed more than one time during
the course of the year.
All of these takes are anticipated to be
in the form of behavioral harassment
(TTS and behavioral reaction) and no
injurious takes of delphinids from sonar
and other active acoustic stressors or
explosives are requested or proposed for
authorization. Further, the majority of
takes are anticipated to be by behavioral
harassment in the form of mild
responses. Research and observations
show that if delphinids are exposed to
sonar or other active acoustic sources
they may react in a number of ways
depending on their experience with the
sound source and what activity they are
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10009
engaged in at the time of the acoustic
exposure. Delphinids may not react at
all until the sound source is
approaching within a few hundred
meters to within a few kilometers
depending on the environmental
conditions and species. Delphinids that
are exposed to activities that involve the
use of sonar and other active acoustic
sources may alert, ignore the stimulus,
change their behaviors or vocalizations,
avoid the sound source by swimming
away or diving, or be attracted to the
sound source (Richardson, 1995;
Nowacek, 2007; Southall et al., 2007;
Finneran and Jenkins, 2012). Research
has demonstrated that Alaska Resident
killer whales may routinely move over
long large distances (Andrews and
Matkin, 2014; Fearnbach et al., 2013). In
a similar documented long-distance
movement, an Eastern North Pacific
Offshore stock killer whale tagged off
San Clemente Island, California, moved
(over a period of 147 days) to waters off
northern Mexico, then north to Cook
Inlet, Alaska, and finally (when the tag
ceased transmitting) to coastal waters off
Southeast Alaska (Falcone and Schorr,
2014). Given these findings, temporary
displacement due to avoidance of
training activities are therefore unlikely
to have biological significance to
individual animals.
Delphinid species generally travel in
large pods and should be visible from a
distance in order to implement
mitigation measures and reduce
potential impacts. Many of the recorded
delphinid vocalizations overlap with
the MFAS/HFAS TTS frequency range
(2–20 kHz); however, as noted above,
NMFS does not anticipate TTS of a
serious degree or extended duration to
occur as a result of exposure to MFAS/
HFAS. Recovery from a threshold shift
(TTS) can take a few minutes to a few
days, depending on the exposure
duration, sound exposure level, and the
magnitude of the initial shift, with
larger threshold shifts and longer
exposure durations requiring longer
recovery times (Finneran et al., 2005;
Finneran and Schlundt, 2010; Mooney
et al., 2009a; Mooney et al., 2009b).
However, large threshold shifts are not
anticipated for these activities because
of the unlikelihood that animals will
remain within the ensonified area (due
to the short duration of the majority of
exercises, the speed of the vessels, and
the short distance within which the
animal would need to approach the
sound source) at high levels for the
duration necessary to induce larger
threshold shifts. Threshold shifts do not
necessarily affect all hearing frequencies
equally, so some threshold shifts may
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not interfere with an animal’s hearing of
biologically relevant sounds. Their size
and detectability makes it unlikely that
these animals would be exposed to the
higher energy or pressure expected to
result in more severe effects.
The predicted effects to delphinids
are unlikely to cause long-term
consequences for individual animals or
populations. The GOA TMAA activities
are not expected to occur in an area/
time of specific importance for
reproductive, feeding, or other known
critical behaviors for delphinids. Stocks
of delphinid species found in the Study
Area are not depleted under the MMPA,
nor are they listed under the ESA.
Consequently, the activities are not
expected to adversely impact rates of
recruitment or survival of delphinid
species.
Porpoises—The Navy’s acoustic
analysis predicts that 16,244 instances
of Level B harassment (TTS and
behavioral) of Dall’s porpoise (Alaska
stock) and 7,410 instances of Level B
harassment of harbor porpoise (GOA
and Southeast Alaska stocks) may occur
each year from sonar and other active
acoustic sources and explosives
associated with training and testing
activities in the Study Area. These
represent a limited number of takes
relative to population estimates for
porpoise stocks in the Study Area (Table
6). When the numbers of takes for Dall’s
and harbor porpoise are compared to
their respective estimated stock
abundances and if one assumes that
each take happens to a separate animal,
less than 20 percent of the Alaska stock
of Dall’s porpoise, and less than 18
percent of the GOA and Southeast
Alaska stocks of harbor porpoise would
be harassed (behaviorally) during the
course of a year. Because the estimates
given above represent the total number
of exposures and not necessarily the
number of individuals exposed, it is
more likely that fewer individuals
would be taken, but a subset would be
taken more than one time per year.
Behavioral responses can range from
a mild orienting response, or a shifting
of attention, to flight and panic
(Richardson, 1995; Nowacek, 2007;
Southall et al., 2007). Acoustic analysis
(factoring in the post-model correction
for avoidance and mitigation) also
predicted that 5 Dall’s porpoises might
be exposed to sound levels from sonar
and other active acoustic stressors and
explosives likely to result in PTS or
injury (Level A harassment).
The number of Dall’s and harbor
porpoise behaviorally harassed by
exposure to MFAS/HFAS in the Study
Area is generally higher than the other
species. This is due to the low Level B
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harassment threshold (we assume for
the purpose of estimating take that all
harbor porpoises exposed to 120 dB or
higher MFAS/HFAS will be taken by
Level B behavioral harassment), which
essentially makes the ensonified area of
effects significantly larger than for the
other species. However, the fact that the
threshold is a step function and not a
curve (and assuming uniform density)
means that the vast majority of the takes
occur in the very lowest levels that
exceed the threshold (it is estimated that
approximately 80 percent of the takes
are from exposures to 120 dB–126 dB),
which means that anticipated
behavioral effects are not expected to be
severe (e.g., temporary avoidance). As
mentioned above, an animal’s exposure
to a higher received level is more likely
to result in a behavioral response that is
more likely to adversely affect the
health of an animal. Animals that do not
exhibit a significant behavioral reaction
would likely recover from any incurred
costs, which reduces the likelihood of
long-term consequences, such as
reduced fitness, for the individual or
population.
Animals that experience hearing loss
(TTS or PTS) may have reduced ability
to detect relevant sounds such as
predators, prey, or social vocalizations.
Some porpoise vocalizations might
overlap with the MFAS/HFAS TTS
frequency range (2–20 kHz). Recovery
from a threshold shift (TTS; partial
hearing loss) can take a few minutes to
a few days, depending on the exposure
duration, sound exposure level, and the
magnitude of the initial shift, with
larger threshold shifts and longer
exposure durations requiring longer
recovery times (Finneran et al., 2005;
Mooney et al., 2009a; Mooney et al.,
2009b; Finneran and Schlundt, 2010).
More severe shifts may not fully recover
and thus would be considered PTS.
However, large degrees of PTS are not
anticipated for these activities because
of the unlikelihood that animals will
remain within the ensonified area (due
to the short duration of the majority of
exercises, the speed of the vessels, and
the short distance within which the
animal would need to approach the
sound source) at high levels for the
duration necessary to induce larger
threshold shifts. Threshold shifts do not
necessarily affect all hearing frequencies
equally, so some threshold shifts may
not interfere with an animal hearing
biologically relevant sounds. The likely
consequences to the health of an
individual that incurs PTS can range
from mild to more serious, depending
upon the degree of PTS and the
frequency band it is in, and many
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animals are able to compensate for the
shift, although it may include energetic
costs. Furthermore, likely avoidance of
intense activity and sound coupled with
mitigation measures would further
reduce the potential for severe PTS
exposures to occur. If a marine mammal
is able to approach a surface vessel
within the distance necessary to incur
PTS, the likely speed of the vessel
(nominal 10–15 knots) would make it
very difficult for the animal to remain
in range long enough to accumulate
enough energy to result in more than a
mild case of PTS.
Harbor porpoises have been observed
to be especially sensitive to human
activity (Tyack et al., 2011; Pirotta et al.,
2012). The information currently
available regarding harbor porpoises
suggests a very low threshold level of
response for both captive (Kastelein et
al., 2000; Kastelein et al., 2005) and
wild (Johnston, 2002) animals. Southall
et al. (2007) concluded that harbor
porpoises are likely sensitive to a wide
range of anthropogenic sounds at low
received levels (∼ 90 to 120 dB).
Research and observations of harbor
porpoises for other locations show that
this small species is wary of human
activity and will display profound
avoidance behavior for anthropogenic
sound sources in many situations at
levels down to 120 dB re 1 mPa
(Southall, 2007). Harbor porpoises
routinely avoid and swim away from
large motorized vessels (Barlow et al.,
1988; Evans et al., 1994; Palka and
Hammond, 2001; Polacheck and
Thorpe, 1990). The vaquita, which is
closely related to the harbor porpoise in
the Study Area, appears to avoid large
vessels at about 2,995 ft. (913 m)
(Jaramillo-Legorreta et al., 1999). The
assumption is that the harbor porpoise
would respond similarly to large Navy
vessels, possibly prior to
commencement of sonar or explosive
activity (i.e., pre-activity avoidance).
Harbor porpoises may startle and
temporarily leave the immediate area of
the training or testing until after the
event ends.
ASW training exercises using MFAS/
HFAS generally last for 2–16 hours, and
may have intervals of non-activity in
between. In addition, the Navy does not
typically conduct ASW exercises in the
same locations. Given the average length
of ASW exercises (times of continuous
sonar use) and typical vessel speed,
combined with the fact that the majority
of porpoises in the Study Area would
not likely remain in an area for
successive days, it is unlikely that an
animal would be exposed to MFAS/
HFAS at levels likely to result in a
substantive response (e.g., interruption
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of feeding) that would then be carried
on for more than one day or on
successive days. Thompson et al. (2013)
showed that seismic surveys conducted
over a 10-day period in the North Sea
did not result in the broad-scale
displacement of harbor porpoises away
from preferred habitat. The harbor
porpoises were observed to leave the
area at the onset of survey, but returned
within a few hours, and the overall
response of the porpoises decreased
over the 10-day period.
Considering the information above,
the predicted effects to Dall’s and harbor
porpoise are unlikely to cause long-term
consequences for individual animals or
the population. The GOA activities are
not expected to occur in an area/time of
specific importance for reproductive,
feeding, or other known critical
behaviors for Dall’s and harbor
porpoise. Stocks of Dall’s and harbor
porpoise are not listed as depleted
under the MMPA. Consequently, the
activities are not expected to adversely
impact annual rates of recruitment or
survival of porpoises.
Beaked Whales—Acoustic analysis
predicts that 401 Baird’s beaked whales
(Alaska stock), 2,544 Cuvier’s beaked
whales (Alaska stock), and 1,153
Stejneger’s beaked whales (Alaska stock)
will be taken annually by Level B
harassment from exposure to sonar and
other active acoustic stressors. These
takes are anticipated to be in the form
of behavioral harassment (mainly
behavioral reaction and some TTS) and
no injurious takes of beaked whales
from sonar and other active acoustic
stressors or explosives are requested or
proposed. Relative to population size,
training activities are anticipated to
result only in a limited number of takes.
Because the estimates given above
represent the total number of exposures
and not necessarily the number of
individuals exposed, it is more likely
that fewer individuals would be taken,
but a subset would be taken more than
one time per year. There are currently
no reliable abundance estimates for
Alaska stocks of Baird’s, Cuvier’s, and
Stejner’s beaked whales (Muto and
Angliss, 2015).
As is the case with harbor porpoises,
beaked whales have been shown to be
particularly sensitive to sound and
therefore have been assigned a lower
harassment threshold based on
observations of wild animals by
McCarthy et al. (2011) and Tyack et al.
(2011). The fact that the Level B
harassment threshold is a step function
(The Navy has adopted an unweighted
140 dB re 1 mPa SPL threshold for
significant behavioral effects for all
beaked whales) and not a curve (and
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assuming uniform density) means that
the vast majority of the takes occur in
the very lowest levels that exceed the
threshold (it is estimated that
approximately 80 percent of the takes
are from exposures to 140 dB to 146 dB),
which means that the anticipated effects
for the majority of exposures are not
expected to be severe (As mentioned
above, an animal’s exposure to a higher
received level is more likely to result in
a behavioral response that is more likely
to adversely affect the health of an
animal). Further, Moretti et al. (2014)
recently derived an empirical risk
function for Blainville’s beaked whale
that predicts there is a 0.5 probability of
disturbance at a received level of 150 dB
(CI: 144–155), suggesting that in some
cases the current Navy step function
may over-estimate the effects of an
activity using sonar on beaked whales.
Irrespective of the Moretti et al. (2014)
risk function, NMFS’ analysis assumes
that all of the beaked whale Level B
takes that are proposed for authorization
will occur, and we base our negligible
impact determination, in part, on the
fact that these exposures would mainly
occur at the very lowest end of the 140dB behavioral harassment threshold
where behavioral effects are expected to
be much less severe and generally
temporary in nature.
Behavioral responses can range from
a mild orienting response, or a shifting
of attention, to flight and panic
(Richardson, 1995; Nowacek, 2007;
Southall et al., 2007; Finneran and
Jenkins, 2012). Research has also shown
that beaked whales are especially
sensitive to the presence of human
activity (Tyack et al., 2011; Pirotta et al.,
2012). Beaked whales have been
documented to exhibit avoidance of
human activity or respond to vessel
presence (Pirotta et al., 2012). Beaked
whales were observed to react
negatively to survey vessels or low
altitude aircraft by quick diving and
other avoidance maneuvers, and none
were observed to approach vessels
(Wursig et al., 1998). Some beaked
whale vocalizations may overlap with
the MFAS/HFAS TTS frequency range
(2–20 kHz); however, as noted above,
NMFS does not anticipate TTS of a
serious degree or extended duration to
occur as a result of exposure to MFA/
HFAS. Recovery from a threshold shift
(TTS) can take a few minutes to a few
days, depending on the exposure
duration, sound exposure level, and the
magnitude of the initial shift, with
larger threshold shifts and longer
exposure durations requiring longer
recovery times (Finneran et al., 2005;
Mooney et al., 2009a; Mooney et al.,
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2009b; Finneran and Schlundt, 2010).
Large threshold shifts are not
anticipated for these activities because
of the unlikelihood that animals will
remain within the ensonified area (due
to the short duration of the majority of
exercises, the speed of the vessels, and
the short distance within which the
animal would need to approach the
sound source) at high levels for the
duration necessary to induce larger
threshold shifts. Threshold shifts do not
necessarily affect all hearing frequencies
equally, so some threshold shifts may
not interfere with an animal’s hearing of
biologically relevant sounds.
It has been speculated for some time
that beaked whales might have unusual
sensitivities to sonar sound due to their
likelihood of stranding in conjunction
with MFAS use. Research and
observations show that if beaked whales
are exposed to sonar or other active
acoustic sources they may startle, break
off feeding dives, and avoid the area of
the sound source to levels of 157 dB re
1 mPa, or below (McCarthy et al., 2011).
Acoustic monitoring during actual sonar
exercises revealed some beaked whales
continuing to forage at levels up to 157
dB re 1 mPa (Tyack et al. 2011). Stimpert
et al. (2014) tagged a Baird’s beaked
whale, which was subsequently exposed
to simulated MFAS. Changes in the
animal’s dive behavior and locomotion
were observed when received level
reached 127 dB re 1mPa. However,
Manzano-Roth et al. (2013) found that
for beaked whale dives that continued
to occur during MFAS activity,
differences from normal dive profiles
and click rates were not detected with
estimated received levels up to 137 dB
re 1 mPa while the animals were at
depth during their dives. And in
research done at the Navy’s fixed
tracking range in the Bahamas, animals
were observed to leave the immediate
area of the anti-submarine warfare
training exercise (avoiding the sonar
acoustic footprint at a distance where
the received level was ‘‘around 140 dB’’
SPL, according to Tyack et al. [2011])
but return within a few days after the
event ended (Claridge and Durban,
2009; Moretti et al., 2009, 2010; Tyack
et al., 2010, 2011; McCarthy et al.,
2011). Tyack et al. (2011) report that, in
reaction to sonar playbacks, most
beaked whales stopped echolocating,
made long slow ascent to the surface,
and moved away from the sound. A
similar behavioral response study
conducted in Southern California waters
during the 2010–2011 field season
found that Cuvier’s beaked whales
exposed to MFAS displayed behavior
ranging from initial orientation changes
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to avoidance responses characterized by
energetic fluking and swimming away
from the source (DeRuiter et al., 2013b).
However, the authors did not detect
similar responses to incidental exposure
to distant naval sonar exercises at
comparable received levels, indicating
that context of the exposures (e.g.,
source proximity, controlled source
ramp-up) may have been a significant
factor. The study itself found the results
inconclusive and meriting further
investigation. Cuvier’s beaked whale
responses suggested particular
sensitivity to sound exposure as
consistent with results for Blainville’s
beaked whale.
Populations of beaked whales and
other odontocetes on the Bahamas and
other Navy fixed ranges that have been
operating for decades, appear to be
stable. Behavioral reactions (avoidance
of the area of Navy activity) seem likely
in most cases if beaked whales are
exposed to anti-submarine sonar within
a few tens of kilometers, especially for
prolonged periods (a few hours or more)
since this is one of the most sensitive
marine mammal groups to
anthropogenic sound of any species or
group studied to date and research
indicates beaked whales will leave an
area where anthropogenic sound is
present (Tyack et al., 2011; De Ruiter et
al., 2013; Manzano-Roth et al., 2013;
Moretti et al., 2014). Research involving
tagged Cuvier’s beaked whales in the
SOCAL Range Complex reported on by
Falcone and Schorr (2012, 2014)
indicates year-round prolonged use of
the Navy’s training and testing area by
these beaked whales and has
documented movements in excess of
hundreds of kilometers by some of those
animals. Given that some of these
animals may routinely move hundreds
of kilometers as part of their normal
pattern, leaving an area where sonar or
other anthropogenic sound is present
may have little, if any, cost to such an
animal. Photo identification studies in
the SOCAL Range Complex, a Navy
range that is utilized for training and
testing more frequently than the GOA
TMAA Study Area, have identified
approximately 100 individual Cuvier’s
beaked whale individuals with 40
percent having been seen in one or more
prior years, with re-sightings up to 7
years apart (Falcone and Schorr, 2014).
These results indicate long-term
residency by individuals in an
intensively used Navy training and
testing area, which may also suggest a
lack of long-term consequences as a
result of exposure to Navy training and
testing activities. Finally, results from
passive acoustic monitoring estimated
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regional Cuvier’s beaked whale
densities were higher than indicated by
the NMFS’s broad scale visual surveys
for the U.S. west coast (Hildebrand and
McDonald, 2009).
Based on the findings above, it is clear
that the Navy’s long-term ongoing use of
sonar and other active acoustic sources
has not precluded beaked whales from
also continuing to inhabit those areas. In
summary, based on the best available
science, the Navy and NMFS believe
that beaked whales that exhibit a
significant TTS or behavioral reaction
due to sonar and other active acoustic
testing activities would generally not
have long-term consequences for
individuals or populations. Claridge
(2013) speculated that sonar use in a
Bahamas range could have ‘‘a possible
population-level effect’’ on beaked
whales based on lower abundance in
comparison to control sites. In
summary, Claridge suggested that lower
reproductive rates observed at the
Navy’s Atlantic Undersea Test and
Evaluation Center (AUTEC), when
compared to a control site, were due to
stressors associated with frequent and
repeated use of Navy sonar. It is also
important to note that there were some
relevant shortcomings of this study. For
example, all of the re-sighted whales
during the 5-year study at both sites
were female, which Claridge
acknowledged can lead to a negative
bias in the abundance estimation. There
was also a reduced effort and shorter
overall study period at the AUTEC site
that failed to capture some of the
emigration/immigration trends
identified at the control site.
Furthermore, Claridge assumed that the
two sites were identical and therefore
should have equal potential
abundances; when in reality, there were
notable physical differences. The author
also acknowledged that ‘‘information
currently available cannot provide a
quantitative answer to whether frequent
sonar use at [the Bahamas range] is
causing stress to resident beaked
whales,’’ and cautioned that the
outcome of ongoing studies ‘‘is a critical
component to understanding if there are
population-level effects.’’ Moore and
Barlow (2013) have noted a decline in
beaked whale populations in a broad
area of the Pacific Ocean area out to 300
nm from the coast and extending from
the Canadian-U.S. border to the tip of
Baja Mexico. There are scientific caveats
and limitations to the data used for that
analysis, as well as oceanographic and
species assemblage changes on the U.S.
Pacific coast not thoroughly addressed.
Although Moore and Barlow (2013)
have noted a decline in the overall
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beaked whale population along the
Pacific coast, in the small fraction of
that area where the Navy has been
training and testing with sonar and
other systems for decades (the Navy’s
SOCAL Range Complex), higher
densities and long-term residency by
individual Cuvier’s beaked whales
suggest that the decline noted elsewhere
is not apparent where Navy sonar use is
most intense. Navy sonar training and
testing is not conducted along a large
part of the U.S. west coast from which
Moore and Barlow (2013) drew their
survey data. In Southern California,
based on a series of surveys from 2006
to 2008 and a high number encounter
rate, Falcone et al. (2009) suggested the
ocean basin west of San Clemente Island
may be an important region for Cuvier’s
beaked whales given the number of
animals encountered there. Follow-up
research (Falcone and Schorr, 2012,
2014) in this same location suggests that
Cuvier’s beaked whales may have
population sub-units with higher than
expected residency, particularly in the
Navy’s instrumented Southern
California Anti-Submarine Warfare
Range. Encounters with multiple groups
of Cuvier’s and Baird’s beaked whales
indicated not only that they were
prevalent on the range where Navy
routinely trains and tests, but also that
they were potentially present in much
higher densities than had been reported
for anywhere along the U.S. west coast
(Falcone et al., 2009, Falcone and
Schorr, 2012). This finding is also
consistent with concurrent results from
passive acoustic monitoring that
estimated regional Cuvier’s beaked
whale densities were higher where Navy
trains in the SOCAL training and testing
area than indicated by NMFS’s broad
scale visual surveys for the U.S. west
coast (Hildebrand and McDonald, 2009).
NMFS also considered New et al.
(2013) and their mathematical model
simulating a functional link between
foraging energetics and requirements for
survival and reproduction for 21 species
of beaked whales. However, NMFS
concluded that New et al. (2013) model
lacks critical data and accurate inputs
necessary to form valid conclusions
specifically about impacts of
anthropogenic sound from Navy
activities on beaked whale populations.
The study itself notes the need for
‘‘future research,’’ identifies ‘‘key data
needs’’ relating to input parameters that
‘‘particularly affected’’ the model
results, and states only that the use of
the model ‘‘in combination with more
detailed research’’ could help predict
the effects of management actions on
beaked whale species. In short,
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information is not currently available to
specifically support the use of this
model in a project-specific evaluation of
the effects of Navy activities on the
impacted beaked whale species in GOA.
No beaked whales are predicted in the
acoustic analysis to be exposed to sound
levels associated with PTS, other injury,
or mortality. After decades of the Navy
conducting similar activities in the GOA
Study Area without incident, NMFS
does not expect strandings, injury, or
mortality of beaked whales to occur as
a result of training activities. Stranding
events coincident with Navy MFAS use
in which exposure to sonar is believed
to have been a contributing factor were
detailed in the Stranding and Mortality
section of this proposed rule. However,
for some of these stranding events, a
causal relationship between sonar
exposure and the stranding could not be
clearly established (Cox et al., 2006). In
other instances, sonar was considered
only one of several factors that, in their
aggregate, may have contributed to the
stranding event (Freitas, 2004; Cox et
al., 2006). Because of the association
between tactical MFAS use and a small
number of marine mammal strandings,
the Navy and NMFS have been
considering and addressing the
potential for strandings in association
with Navy activities for years. In
addition to a suite of mitigation
measures intended to more broadly
minimize impacts to marine mammals,
the reporting requirements set forth in
this rule ensure that NMFS is notified
immediately (or as soon as clearance
procedures allow) if a stranded marine
mammal is found during or shortly
after, and in the vicinity of, any Navy
training exercise utilizing MFAS, HFAS,
or underwater explosive detonations
(see General Notification of Injured or
Dead Marine Mammals and the
Stranding Response Plan in the
regulatory text below). Additionally,
through the MMPA process (which
allows for adaptive management),
NMFS and the Navy will determine the
appropriate way to proceed in the event
that a causal relationship were to be
found between Navy activities and a
future stranding.
The GOA training activities are not
expected to occur in an area/time of
specific importance for reproductive,
feeding, or other known critical
behaviors for beaked whales. None of
the Pacific stocks for beaked whales
species found in the Study Area are
depleted under the MMPA. The degree
of predicted Level B harassment is
expected to be mild, and no beaked
whales are predicted in the acoustic
analysis to be exposed to sound levels
associated with PTS, other injury, or
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mortality. Consequently, the activities
are not expected to adversely impact
annual rates of recruitment or survival
of beaked whales.
Pinnipeds—The Navy’s acoustic
analysis predicts that the following
numbers of Level B harassment (TTS
and behavioral reaction) may occur
annually from sonar and other active
acoustic stressors associated with
training activities: 1,243 Steller sea lions
(Eastern U.S. and Western U.S. stocks);
5 California sea lions (U.S. stock); 1,428
northern fur seals (Eastern Pacific
stock); 245 northern elephant seals
(California Breeding stock); and 4 harbor
seals (North Kodiak, South Kodiak, and
Prince William Sound stocks). These
represent a limited number of takes
relative to population estimates for
pinniped stocks in the Study Area
(Table 6). When the numbers of
behavioral takes are compared to the
estimated stock abundances, less than 2
percent of each of these stocks would be
behaviorally harassed during the course
of a year. These estimates represents the
total number of exposures and not
necessarily the number of individuals
exposed, as a single individual may be
exposed multiple times over the course
of a year. Based on the distribution
information presented in the LOA
application, it is highly unlikely that
ribbon seals would be encountered in
the Study Area during events involving
use of sonar and other active acoustic
sources or explosives. The acoustic
analysis did not predict any takes of
ribbon seals and NMFS is not
authorizing any takes of this species.
Research has demonstrated that for
pinnipeds, as for other mammals,
recovery from a threshold shift (TTS)
can take a few minutes to a few days,
depending on the exposure duration,
sound exposure level, and the
magnitude of the initial shift, with
larger threshold shifts and longer
exposure durations requiring longer
recovery times (Finneran et al., 2005;
Finneran and Schlundt, 2010; Mooney
et al., 2009a; Mooney et al., 2009b).
However, large threshold shifts are not
anticipated for these activities because
of the unlikelihood that animals will
remain within the ensonified area (due
to the short duration of the majority of
exercises, the speed of the vessels, and
the short distance within which the
animal would need to approach the
sound source) at high levels for the
duration necessary to induce larger
threshold shifts. Threshold shifts do not
necessarily affect all hearing frequencies
equally, so threshold shifts may not
necessarily interfere with an animal’s
ability to hear biologically relevant
sounds.
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Research and observations show that
pinnipeds in the water may be tolerant
of anthropogenic noise and activity (a
review of behavioral reactions by
pinnipeds to impulsive and nonimpulsive noise can be found in
Richardson et al., 1995 and Southall et
al., 2007). Available data, though
limited, suggest that exposures between
approximately 90 and 140 dB SPL do
not appear to induce strong behavioral
responses in pinnipeds exposed to
nonpulse sounds in water (Jacobs and
Terhune, 2002; Costa et al., 2003;
Kastelein et al., 2006c). Based on the
limited data on pinnipeds in the water
exposed to multiple pulses (small
explosives, impact pile driving, and
seismic sources), exposures in the
approximately 150 to 180 dB SPL range
generally have limited potential to
induce avoidance behavior in pinnipeds
(Harris et al., 2001; Blackwell et al.,
2004; Miller et al., 2004). If pinnipeds
are exposed to sonar or other active
acoustic sources they may react in a
number of ways depending on their
experience with the sound source and
what activity they are engaged in at the
time of the acoustic exposure. Pinnipeds
may not react at all until the sound
source is approaching within a few
hundred meters and then may alert,
ignore the stimulus, change their
behaviors, or avoid the immediate area
by swimming away or diving. Houser et
al. (2013) performed a controlled
exposure study involving California sea
lions exposed to a simulated MFAS
signal. The purpose of this Navysponsored study was to determine the
probability and magnitude of behavioral
responses by California sea lions
exposed to differing intensities of
simulated MFAS signals. Behavioral
reactions included increased respiration
rates, prolonged submergence, and
refusal to participate, among others.
Younger animals were more likely to
respond than older animals, while some
sea lions did not respond consistently at
any level. Houser et al.’s findings are
consistent with current scientific
studies and criteria development
concerning marine mammal reactions to
MFAS. Effects on pinnipeds in the
Study Area that are taken by Level B
harassment, on the basis of reports in
the literature as well as Navy
monitoring from past activities, will
likely be limited to reactions such as
increased swimming speeds, increased
surfacing time, or decreased foraging (if
such activity were occurring). Most
likely, individuals will simply move
away from the sound source and be
temporarily displaced from those areas,
or not respond at all. In areas of
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repeated and frequent acoustic
disturbance, some animals may
habituate or learn to tolerate the new
baseline or fluctuations in noise level.
Habituation can occur when an animal’s
response to a stimulus wanes with
repeated exposure, usually in the
absence of unpleasant associated events
(Wartzok et al., 2003). While some
animals may not return to an area, or
may begin using an area differently due
to training and testing activities, most
animals are expected to return to their
usual locations and behavior. Given
their documented tolerance of
anthropogenic sound (Richardson et al.,
1995 and Southall et al., 2007), repeated
exposures of individuals (e.g., harbor
seals) to levels of sound that may cause
Level B harassment are unlikely to
result in hearing impairment or to
significantly disrupt foraging behavior.
As stated above, pinnipeds may
habituate to or become tolerant of
repeated exposures over time, learning
to ignore a stimulus that in the past has
not accompanied any overt threat.
Thus, even repeated Level B
harassment of some small subset of an
overall stock is unlikely to result in any
significant realized decrease in fitness to
those individuals, and would not result
in any adverse impact to the stock as a
whole. Evidence from areas where the
Navy extensively trains and tests
provides some indication of the possible
consequences resulting from those
proposed activities. In the confined
waters of Washington State’s Hood
Canal where the Navy has been training
and intensively testing for decades and
harbor seals are present year-round, the
population level has remained stable
suggesting the area’s carrying capacity
likely has been reached (Jeffries et al.,
2003; Gaydos et al., 2013). Within Puget
Sound there are several locations where
pinnipeds use Navy structures (e.g.,
submarines, security barriers) for
haulouts. Given that animals continue
to choose these areas for their resting
behavior, it would appear there are no
long-term effects or consequences to
those animals as a result of ongoing and
routine Navy activities.
Generally speaking, most pinniped
stocks in the Study Area are thought to
be stable or increasing (Carretta et al.,
2014, 2015). Abundance estimates for
pinniped stocks in the Study Area are
shown in Table 6. Relative to
population size, training activities are
anticipated to result only in a limited
number of takes. No areas of specific
importance for reproduction or feeding
for pinnipeds have been identified in
the Study Area. Consequently, the
activities are not expected to adversely
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impact rates of recruitment or survival
of pinniped species.
Western U.S. stocks of Steller sea
lions are listed as endangered under the
ESA; however, there is no designated
critical habitat Steller sea lions in the
Study Area. As a conservative measure,
the GOA TMAA boundary zone was
specifically drawn to exclude any
nearby critical habitat and associated
terrestrial, air, or aquatic zones. NMFS
is currently engaged in an internal
Section 7 consultation under the ESA
and the outcome of that consultation
will further inform our final
determination.
Long-Term Consequences
The best assessment of long-term
consequences from training activities
will be to monitor the populations over
time within a given Navy range
complex. A U.S. workshop on Marine
Mammals and Sound (Fitch et al., 2011)
indicated a critical need for baseline
biological data on marine mammal
abundance, distribution, habitat, and
behavior over sufficient time and space
to evaluate impacts from humangenerated activities on long-term
population survival. The Navy has
developed monitoring plans for
protected marine mammals occurring on
Navy ranges with the goal of assessing
the impacts of training and testing
activities on marine species and the
effectiveness of the Navy’s current
mitigation practices. Continued
monitoring efforts over time will be
necessary to completely evaluate the
long-term consequences of exposure to
noise sources.
Since 2006 across all Navy range
complexes (in the Atlantic, Gulf of
Mexico, and the Pacific), there have
been more than 80 reports, including
Major Exercise Reports, Annual Exercise
Reports, and Monitoring Reports. For
the Pacific since 2011, there have been
29 monitoring and exercise reports
submitted to NMFS to further research
goals aimed at understanding the Navy’s
impact on the environment as it carries
out its mission to train and test.
In addition to this multi-year record
of reports from across the Navy, there
have also been ongoing Behavioral
Response Study research efforts (in
Southern California and the Bahamas)
specifically focused on determining the
potential effects from Navy midfrequency sonar (Southall et al., 2011,
2012; McCarthy et al., 2011; Tyack et
al., 2011; DeRuiter et al., 2013b;
Goldbogen et al., 2013; Moretti et al.,
2014). This multi-year compendium of
monitoring, observation, study, and
broad scientific research is informative
with regard to assessing the effects of
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Navy training and testing in general.
Given that this record involves many of
the same Navy training activities being
considered for the Study Area and
because it includes all the marine
mammal taxonomic families and many
of the same species, this compendium of
Navy reporting is directly applicable to
assessing locations such as the GOA
TMAA.
In the Hawaii and Southern California
Navy training and testing ranges from
2009 to 2012, Navy-funded marine
mammal monitoring research completed
over 5,000 hours of visual survey effort
covering over 65,000 nautical miles,
sighted over 256,000 individual marine
mammals, took over 45,600 digital
photos and 36 hours of digital video,
attached 70 satellite tracking tags to
individual marine mammals, and
collected over 40,000 hours of passive
acoustic recordings. In Hawaii alone
between 2006 and 2012, there were 21
scientific marine mammal surveys
conducted before, during, or after major
exercises. This monitoring effort is
consistent with other research from
these areas in that there have been no
direct evidence demonstration that
routine Navy training and testing has
negatively impacted marine mammal
populations inhabiting these Navy
ranges. Continued monitoring efforts
over time will be necessary to
completely evaluate the long-term
consequences of exposure to noise
sources. Other research findings related
to the general topic of long-term impacts
are discussed above in the SpeciesSpecific Analysis.
Based on monitoring conducted
before, during, and after Navy training
and testing events since 2006, the
NMFS’ assessment is that it is unlikely
there will be impacts having any longterm consequences to populations of
marine mammals as a result of the
proposed continuation of training and
testing in the ocean areas historically
used by the Navy including the Study
Area. This assessment of likelihood is
based on four indicators from areas in
the Pacific where Navy training and
testing has been ongoing for decades: (1)
Evidence suggesting or documenting
increases in the numbers of marine
mammals present (Calambokidis and
Barlow, 2004; Falcone et al., 2009;
Hildebrand and McDonald, 2009;
Falcone and Shorr, 2012; Calambokidis
et al., 2009a; Berman-Kowalewski et al.,
2010; Moore and Barlow, 2011; Barlow
et al., 2011; Kerosky et al,. 2012;
ˇ
´
Smultea et al., 2013; Sirovic et al.,
2015), (2) examples of documented
presence and site fidelity of species and
long-term residence by individual
animals of some species (Hooker et al.,
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2002; McSweeney et al., 2007;
McSweeney et al., 2010; Martin and
Kok, 2011; Baumann-Pickering et al.,
2012; Falcone and Schorr, 2014), (3) use
of training and testing areas for breeding
and nursing activities (Littnan, 2010),
and (4) 6 years of comprehensive
monitoring data indicating a lack of any
observable effects to marine mammal
populations as a result of Navy training
and testing activities.
To summarize, while the evidence
covers most marine mammal taxonomic
suborders, it is limited to a few species
and only suggestive of the general
viability of those species in intensively
used Navy training and testing areas
(Barlow et al., 2011; Calambokidis et al.,
2009b; Falcone et al., 2009; Littnan,
2011; Martin and Kok, 2011; McCarthy
et al., 2011; McSweeney et al., 2007;
McSweeney et al., 2009; Moore and
Barlow, 2011; Tyack et al., 2011;
Southall et al., 2012a; Melcon, 2012;
Goldbogen, 2013; Baird et al., 2013).
However, there is no direct evidence
that routine Navy training and testing
spanning decades has negatively
impacted marine mammal populations
at any Navy Range Complex. Although
there have been a few strandings
associated with use of sonar in other
locations (see U.S. Department of the
Navy, 2013b), Ketten (2012) has recently
summarized, ‘‘to date, there has been no
demonstrable evidence of acute,
traumatic, disruptive, or profound
auditory damage in any marine mammal
as the result of anthropogenic noise
exposures, including sonar.’’ Therefore,
based on the best available science
(Barlow et al., 2011; Carretta et al., 2011;
Falcone et al., 2009; Falcone and
Schorr, 2012, 2014; Jeffries et al., 2003;
Littnan, 2011; Martin and Kok, 2011;
McCarthy et al., 2011; McSweeney et
al., 2007; McSweeney et al., 2009;
Moore and Barlow, 2011; Tyack et al.,
2011; Southall et al., 2012, 2013, 2014;
Manzano-Roth et al., 2013; DeRuiter et
al., 2013b; Goldbogen et al., 2013;
Moretti et al., 2014; Smultea and
ˇ
´
Jefferson, 2014; Sirovic et al. 2015),
including data developed in the series
of 80+ reports submitted to NMFS, we
believe that long-term consequences for
individuals or populations are unlikely
to result from Navy training activities in
the Study Area.
Preliminary Determination
Training activities proposed in the
GOA TMAA Study Area would result in
mainly Level B and some Level A takes,
as summarized in Tables 12 and 13.
Based on best available science, NMFS
concludes that exposures to marine
mammal species and stocks due to GOA
TMAA activities would result in
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individuals experiencing primarily
short-term (temporary and short in
duration) and relatively infrequent
effects of the type or severity not
expected to be additive. In addition,
only a generally small portion of the
stocks and species is likely to be
exposed.
Marine mammal takes from Navy
activities are not expected to impact
annual rates of recruitment or survival
and will therefore not result in
population-level impacts for the
following reasons:
• Most acoustic exposures (greater
than 99 percent) would be within the
non-injurious TTS or behavioral effects
zones (Level B harassment consisting of
generally temporary modifications in
behavior) and none of the estimated
exposures would result in mortality.
• As mentioned earlier, an animal’s
exposure to a higher received level is
more likely to result in a behavioral
response that is more likely to adversely
affect the health of the animal. For low
frequency cetaceans (mysticetes) in the
Study Area, most Level B exposures will
occur at received levels less than 156
dB. The majority of estimated
odontocete takes from MFAS/HFAS (at
least for hull-mounted sonar, which is
responsible for most of the sonar-related
takes) also result from exposures to
received levels less than 156 dB.
Therefore, the majority of Level B takes
are expected to be in the form of milder
responses (i.e., lower-level exposures
that still rise to the level of a take, but
would likely be in the less severe range
of responses that qualify as a take), and
are not expected to have deleterious
impacts on the fitness of any
individuals. Marine mammal densities
inputted into the acoustic effects model
are also conservative, particularly when
considering species for which data in
portions of the Study Area is limited,
and when considering the seasonal
migrations that extend throughout the
Study Area.
• Acoustic disturbances caused by
Navy sonar and explosives are shortterm, intermittent, and (in the case of
sonar) transitory. Even when an
animal’s exposure to active sonar may
be more than one time, the intermittent
nature of the sonar signal, the signal’s
low duty cycle (MFAS has a typical
ping of every 50 seconds), and the fact
that both the vessel and animal are
moving, provide a very small chance
that exposure to active sonar for
individual animals and stocks would be
repeated over extended periods of time.
Consequently, we would not expect the
Navy’s activities to create conditions of
long-term, continuous underwater noise
leading to habitat abandonment or long-
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10015
term hormonal or physiological stress
responses in marine mammals.
• Range complexes where intensive
training and testing have been occurring
for decades have populations of
multiple species with strong site fidelity
(including highly sensitive resident
beaked whales at some locations) and
increases in the number of some
species. Populations of beaked whales
and other odontocetes in the Bahamas,
and in other Navy fixed ranges that have
been operating for tens of years, appear
to be stable.
• Navy monitoring of Navy-wide
activities since 2006 has documented
hundreds of thousands of marine
mammals on the range complexes and
there are only two instances of overt
behavioral change that have been
observed.
• Navy monitoring of Navy-wide
activities since 2006 has documented no
demonstrable instances of injury to
marine mammals as a result of nonimpulsive acoustic sources.
• In at least three decades of similar
Navy activities, only one instance of
injury to marine mammals (March 25,
2011; three long-beaked common
dolphin off Southern California) has
occurred as a known result of training
or testing using an impulsive source
(underwater explosion). Of note, the
time-delay firing underwater explosive
training activity implicated in the
March 4 incident is not proposed for the
training activities in the GOA Study
Area.
• The protective measures described
in the Proposed Mitigation section
above are designed to reduce vessel
strike potential and avoid sound
exposures that may cause serious injury,
and to result in the least practicable
adverse effect on marine mammal
species or stocks.
Based on this analysis of the likely
effects of the specified activity on
marine mammals and their habitat,
which includes consideration of the
materials provided in the Navy’s LOA
application and GOA DSEIS/OEIS, and
dependent upon the implementation of
the mitigation and monitoring measures,
NMFS finds that the total marine
mammal take from the Navy’s training
and testing activities in the GOA Study
Area will have a negligible impact on
the affected marine mammal species or
stocks. NMFS proposes to issue
regulations for these activities in order
to prescribe the means of effecting the
least practicable adverse impact on
marine mammal species or stocks and
their habitat, and to set forth
requirements pertaining to the
monitoring and reporting of that taking.
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Subsistence Harvest of Marine
Mammals
There are no relevant subsistence uses
of marine mammals implicated by this
action. None of the proposed training
activities in the Study Area occur where
traditional Arctic subsistence hunting
exists. Therefore, NMFS has
preliminarily determined that the total
taking affecting species or stocks would
not have an unmitigable adverse impact
on the availability of such species or
stocks for taking for subsistence
purposes.
ESA
There are eight marine mammal
species under NMFS jurisdiction that
are listed as endangered or threatened
under the ESA with confirmed or
possible occurrence in the Study Area:
Blue whale, fin whale, humpback
whale, sei whale, sperm whale, gray
whale (Western North Pacific stock),
North Pacific right whale, and Steller
sea lion (Western U.S. stock). The Navy
will consult with NMFS pursuant to
section 7 of the ESA, and NMFS will
also consult internally on the issuance
of a LOA under section 101(a)(5)(A) of
the MMPA for GOA TMAA activities.
Consultation will be concluded prior to
a determination on the issuance of the
final rule and a LOA.
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NEPA
NMFS is a cooperating agency on the
Navy’s GOA DSEIS/OEIS, which was
prepared and released to the public
August 23, 2014. Upon completion, the
GOA Final SEIS/OEIS will be made
available for public review and posted
on NMFS’ Web site: https://
www.nmfs.noaa.gov/pr/permits/
incidental/military.htm. NMFS intends
to adopt the GOA Final SEIS/OEIS, if
adequate and appropriate. Currently, we
believe that the adoption of the GOA
Final SEIS/OEIS will allow NMFS to
meet its responsibilities under NEPA for
the issuance of regulations and LOA for
GOA TMAA. If the GOA SEIS/OEIS is
deemed inadequate by NMFS, NMFS
would supplement the existing analysis
to ensure that we comply with NEPA
prior to issuing the final rule and LOA.
Classification
The Office of Management and Budget
has determined that this proposed rule
is not significant for purposes of
Executive Order 12866.
Pursuant to the Regulatory Flexibility
Act (RFA), the Chief Counsel for
Regulation of the Department of
Commerce has certified to the Chief
Counsel for Advocacy of the Small
Business Administration that this
proposed rule, if adopted, would not
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have a significant economic impact on
a substantial number of small entities.
The RFA requires federal agencies to
prepare an analysis of a rule’s impact on
small entities whenever the agency is
required to publish a notice of proposed
rulemaking. However, a federal agency
may certify, pursuant to 5 U.S.C. 605
(b), that the action will not have a
significant economic impact on a
substantial number of small entities.
The Navy is the sole entity that would
be affected by this rulemaking, and the
Navy is not a small governmental
jurisdiction, small organization, or small
business, as defined by the RFA. Any
requirements imposed by an LOA
issued pursuant to these regulations,
and any monitoring or reporting
requirements imposed by these
regulations, would be applicable only to
the Navy. NMFS does not expect the
issuance of these regulations or the
associated LOA to result in any impacts
to small entities pursuant to the RFA.
Because this action, if adopted, would
directly affect the Navy and not a small
entity, NMFS concludes the action
would not result in a significant
economic impact on a substantial
number of small entities.
List of Subjects in 50 CFR Part 218
Exports, Fish, Imports, Incidental
take, Indians, Labeling, Marine
mammals, Navy, Penalties, Reporting
and recordkeeping requirements,
Seafood, Sonar, Transportation.
Dated: February 17, 2016.
Samuel D. Rauch III,
Deputy Assistant Administrator for
Regulatory Programs, National Marine
Fisheries Service.
For reasons set forth in the preamble,
50 CFR part 218 is proposed to be
amended as follows:
PART 218—REGULATIONS
GOVERNING THE TAKING AND
IMPORTING OF MARINE MAMMALS
1. The authority citation for part 218
continues to read as follows:
■
Authority: 16 U.S.C. 1361 et seq.
Subpart N—[Removed and Reserved]
3. Remove and reserve subpart N,
consisting of §§ 218.120 through
218.129.
■ 4. Subpart P is added to part 218 to
read as follows:
■
Subpart P—Taking and Importing Marine
Mammals; U.S. Navy’s Gulf of Alaska
Temporary Maritime Activities Area (GOA
TMAA) Study Area
Sec.
218.150 Specified activity and specified
geographical region.
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218.151 Effective dates.
218.152 Permissible methods of taking.
218.153 Prohibitions.
218.154 Mitigation.
218.155 Requirements for monitoring and
reporting.
218.156 Applications for letters of
authorization.
218.157 Letters of authorization.
218.158 Renewal and modifications of
letters of authorization and adaptive
management.
Subpart P—Taking and Importing
Marine Mammals; U.S. Navy’s Gulf of
Alaska Temporary Maritime Activities
Area (GOA TMAA) Study Area
§ 218.150 Specified activity and specified
geographical region.
(a) Regulations in this subpart apply
only to the U.S. Navy for the taking of
marine mammals that occurs in the area
outlined in paragraph (b) of this section
and that occurs incidental to the
activities described in paragraph (c) of
this section.
(b) The taking of marine mammals by
the Navy is only authorized if it occurs
within the GOA TMAA Study Area,
which is bounded by a hexagon with the
following six corners: 57°30′° N. lat.,
141°30′° W. long.; 59°36′° N. lat.,
148°10′° W. long.; 58°57′° N. lat.,
150°04′° W. long.; 58°20′° N. lat.,
151°00′° W. long.; 57°16′° N. lat.,
151°00′° W. long.; and 55°30′° N. lat.,
142°00′° W. long.
(c) The taking of marine mammals by
the Navy is only authorized if it occurs
incidental to the following activities:
(1) Sonar and other Active Sources
Used During Training:
(i) Mid-frequency (MF) Source
Classes:
(A) MF1—an average of 541 hours per
year.
(B) MF3—an average of 48 hours per
year.
(C) MF4—an average of 53 hours per
year.
(D) MF5—an average of 25 items per
year.
(E) MF6—an average of 21 items per
year.
(F) MF11—an average of 78 hours per
year.
(ii) High-frequency (HF) Source
Classes:
(A) HF1—an average of 24 hours per
year.
(B) HF6—an average of 80 items per
year.
(iii) Anti-Submarine Warfare (ASW)
Source Classes:
(A) ASW2—an average of 80 hours
per year.
(B) ASW3—an average of 546 hours
per year.
(C) ASW4—an average 4 items per
year.
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(iv) Torpedoes (TORP):
(A) TORP2—an average of 5 items per
year.
(B) [Reserved]
(2) Impulsive Source Detonations
During Training:
(i) Explosive Classes:
(A) E5 (>5 to 10 pound [lb] net
explosive weight (NEW))—an average of
112 detonations per year.
(B) E6 (>10 to 20 lb NEW)—an average
of 2 detonations per year.
(C) E7 (>20 to 60 lb NEW)—an average
of 4 detonations per year.
(D) E8 (>60 to 100 lb NEW)—an
average of 6 detonations per year.
(E) E9 (>100 to 250 lb NEW)—an
average of 142 detonations per year.
(F) E10 (>250 to 500 lb NEW)—an
average of 32 detonations per year.
(G) E11 (>500 to 650 lb NEW)—an
average of 2 detonations per year.
(H) E12 (>650 to 1,000 lb NEW)—an
average of 4 detonations per year.
(ii) [Reserved]
§ 218.151
Effective dates.
Regulations in this subpart are
effective May 4, 2016, through May 3,
2021.
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§ 218.152
Permissible methods of taking.
(a) Under letter of authorization
(LOA) issued pursuant to §§ 216.106
and 218.157 of this chapter, the holder
of the LOA may incidentally, but not
intentionally, take marine mammals
within the area described in § 218.150,
provided the activity is in compliance
with all terms, conditions, and
requirements of these regulations and
the LOA.
(b) The activities identified in
§ 218.150(c) must be conducted in a
manner that minimizes, to the greatest
extent practicable, any adverse impacts
on marine mammals and their habitat.
(c) The incidental take of marine
mammals under the activities identified
in § 218.150(c) is limited to the
following species, by the identified
method of take and the indicated
number of times:
(1) Level B Harassment for all
Training Activities:
(i) Mysticetes:
(A) Blue whale (Balaenoptera
musculus), Eastern North Pacific—475
(an average of 95 per year).
(B) Fin whale (Balaenoptera
physalus), Northeast Pacific—12,910 (an
average of 2,582 per year).
(C) Humpback whale (Megaptera
novaeangliae), Central North Pacific—
645 (an average of 129 per year).
(D) Humpback whale (Megaptera
novaeangliae), Western North Pacific—
50 (an average of 10 per year).
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(E) Minke whale (Balaenoptera
acutorostrata), Alaska—435 (an average
of 87 per year).
(F) North Pacific right whale
(Eubalaena japonica), Eastern North
Pacific—35 (an average of 7 per year).
(G) Sei whale (Balaenoptera borealis),
Eastern North Pacific—65 (an average of
13 per year).
(ii) Odontocetes:
(A) Baird’s beaked whale (Berardius
bairdii), Alaska—2,005 (an average of
401 per year).
(B) Cuvier’s beaked whale (Ziphius
cavirostris), Alaska—12,720 (an average
of 2,544 per year).
(C) Dall’s porpoise (Phocoenoidea
dalli), Alaska—81,220 (an average of
16,244 per year).
(D) Harbor porpoise (Phocoena
phocoena), GOA—27,420 (an average of
5,484 per year).
(E) Harbor porpoise (Phocoena
phocoena), Southeast Alaska—9,630 (an
average of 1,926 per year).
(F) Killer whale (Orcinus orca),
Alaska Resident—2,820 (an average of
564 per year).
(G) Killer whale (Orcinus orca),
Eastern North Pacific Offshore—265 (an
average of 53 per year).
(H) Killer whale (Orcinus orca), AT1
Transient—5 (an average of 1 per year).
(I) Killer whale (Orcinus orca), GOA,
Aleutian Island, and Bearing Sea
Transient—720 (an average of 144 per
year).
(J) Pacific white-sided dolphin
(Lagenorhynchus obliquidens), North
Pacific—9,815 (an average of 1,963 per
year).
(K) Stejneger’s beaked whale
(Mesoplodon stejnegeri), Alaska—5,765
(an average of 1,153 per year).
(L) Sperm whale (Physeter
macrocephalus), North Pacific—985 (an
average of 197 per year).
(iii) Pinnipeds:
(A) California sea lion (Zalophus
californianus), U.S.—25 (an average of 5
per year).
(B) Steller sea lion (Eumetopias
jubatus), Eastern U.S.—3,355 (an
average of 671 per year).
(C) Steller sea lion (Eumetopias
jubatus), Western U.S.—2,860 (an
average of 572 per year).
(D) Harbor seal (Phoca vitulina),
North Kodiak—5 (an average of 1 per
year).
(E) Harbor seal (Phoca vitulina), South
Kodiak—5 (an average of 1 per year).
(F) Harbor seal (Phoca vitulina),
Prince William Sound—10 (an average
of 2 per year).
(G) Northern elephant seal (Mirounga
angustirostris), California Breeding—
1,225 (an average of 245 per year).
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10017
(H) Northern fur seal (Callorhinus
ursinus), Eastern Pacific—7,140 (an
average of 1,428 per year).
(2) Level A Harassment for all
Training Activities:
(i) Odontocetes:
(A) Dall’s porpoise (Phocoenoidea
dalli), Alaska—25 (an average of 5 per
year).
(B) [Reserved]
(ii) [Reserved]
§ 218.153
Prohibitions.
Notwithstanding takings
contemplated in § 218.152 and
authorized by an LOA issued under
§§ 216.106 and 218.157 of this chapter,
no person in connection with the
activities described in § 218.150 may:
(a) Take any marine mammal not
specified in § 218.152(c);
(b) Take any marine mammal
specified in § 218.152(c) other than by
incidental take as specified in
§ 218.152(c);
(c) Take a marine mammal specified
in § 218.152(c) if such taking results in
more than a negligible impact on the
species or stocks of such marine
mammal; or
(d) Violate, or fail to comply with, the
terms, conditions, and requirements of
these regulations or an LOA issued
under §§ 216.106 and 218.157 of this
chapter.
§ 218.154
Mitigation.
(a) When conducting training
activities, as identified in § 218.150, the
mitigation measures contained in the
LOA issued under §§ 216.106 and
218.157 of this chapter must be
implemented. These mitigation
measures include, but are not limited to:
(1) Lookouts.The Navy shall have two
types of lookouts for the purposes of
conducting visual observations: Those
positioned on ships; and those
positioned ashore, in aircraft, or on
boats. The following are protective
measures concerning the use of
lookouts.
(i) Lookouts positioned on surface
ships shall be dedicated solely to
diligent observation of the air and
surface of the water. Their observation
objectives shall include, but are not
limited to, detecting the presence of
biological resources and recreational or
fishing boats, observing mitigation
zones, and monitoring for vessel and
personnel safety concerns.
(ii) Due to manning and space
restrictions on aircraft, small boats, and
some Navy ships, lookouts for these
platforms may be supplemented by the
aircraft crew or pilot, boat crew, range
site personnel, or shore-side personnel.
Lookouts positioned in minimally
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manned platforms may be responsible
for tasks in addition to observing the air
or surface of the water (e.g., navigation
of a helicopter or small boat). However,
all lookouts shall, considering personnel
safety, practicality of implementation,
and impact on the effectiveness of the
activity, comply with the observation
objectives described above for lookouts
positioned on ships.
(iii) All personnel standing watch on
the bridge, Commanding Officers,
Executive Officers, maritime patrol
aircraft aircrews, anti-submarine warfare
helicopter crews, civilian equivalents,
and lookouts shall successfully
complete the United States Navy Marine
Species Awareness Training prior to
standing watch or serving as a lookout.
(iv) Lookout measures for nonimpulsive sound:
(A) With the exception of vessels less
than 65 ft (20 m) in length, ships using
hull-mounted mid-frequency active
sonar sources associated with antisubmarine warfare activities at sea shall
have two Lookouts at the forward
position of the vessel.
(B) While using hull-mounted midfrequency active sonar sources
associated with anti-submarine warfare
activities at sea, vessels less than 65 ft
(20 m) in length shall have one lookout
at the forward position of the vessel due
to space and manning restrictions.
(C) During non-hull mounted midfrequency active sonar training
activities, Navy aircraft participating in
exercises at sea shall conduct and
maintain, when operationally feasible
and safe, surveillance for marine species
of concern as long as it does not violate
safety constraints or interfere with the
accomplishment of primary operational
duties. Helicopters shall observe/survey
the vicinity of an anti-submarine
warfare training event for 10 minutes
before the first deployment of active
(dipping) sonar in the water.
(D) Ships or aircraft conducting nonhull-mounted mid-frequency active
sonar, such as helicopter dipping sonar
systems, shall maintain one lookout.
(E) Ships conducting high-frequency
active sonar shall maintain one lookout.
(v) Lookout measures for explosives
and impulsive sound:
(A) Aircraft conducting explosive
signal underwater sound buoy activities
using >0.5–2.5 lb. NEW shall have one
lookout.
(B) Surface vessels or aircraft
conducting small-, medium-, or largecaliber gunnery exercises against a
surface target shall have one lookout.
From the intended firing position,
trained lookouts shall survey the
mitigation zone for marine mammals
prior to commencement and during the
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exercise as long as practicable. Towing
vessels, if applicable, shall also
maintain one lookout. If a marine
mammal is sighted in the vicinity of the
exercise, the tow vessel shall
immediately notify the firing vessel in
order to secure gunnery firing until the
area is clear.
(C) Aircraft conducting explosive
bombing exercises shall have one
lookout and any surface vessels
involved shall have trained Lookouts. If
surface vessels are involved, lookouts
shall survey for floating kelp and marine
mammals. Aircraft shall visually survey
the target and buffer zone for marine
mammals prior to and during the
exercise. The survey of the impact area
shall be made by flying at 1,500 ft. (460
m) or lower, if safe to do so, and at the
slowest safe speed. Release of ordnance
through cloud cover is prohibited:
Aircraft must be able to actually see
ordnance impact areas. Survey aircraft
should employ most effective search
tactics and capabilities.
(D) When aircraft are conducting
missile exercises against a surface target,
the Navy shall have one Lookout
positioned in an aircraft. Aircraft shall
visually survey the target area for
marine mammals. Visual inspection of
the target area shall be made by flying
at 1,500 ft. (457 m) or lower, if safe to
do so, and at slowest safe speed. Firing
or range clearance aircraft must be able
to actually see ordnance impact areas.
(E) Ships conducting explosive and
non-explosive gunnery exercises shall
have one Lookout on the ship. This may
be the same lookout described in
paragraph (B) above for surface vessels
conducting small-, medium-, or largecaliber gunnery exercises when that
activity is conducted from a ship against
a surface target.
(F) During sinking exercises, two
Lookouts shall be used. One lookout
shall be positioned in an aircraft and
one lookout shall be positioned on a
vessel.
(vi) Lookout measures for physical
strike and disturbance:
(A) While underway, surface ships
shall have at least one lookout.
(B) [Reserved]
(vii) Lookout measures for nonexplosive practice munitions:
(A) Gunnery exercises using nonexplosive practice munitions (e.g.,
small-, medium-, and large-caliber)
using a surface target shall have one
lookout.
(B) During non-explosive bombing
exercises one lookout shall be
positioned in an aircraft and trained
lookouts shall be positioned in any
surface vessels involved.
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(C) When aircraft are conducting nonexplosive missile exercises (including
exercises using rockets) against a surface
target, the Navy shall have one lookout
positioned in an aircraft.
(2) Mitigation Zones—The following
are protective measures concerning the
implementation of mitigation zones.
(i) Mitigation zones shall be measured
as the radius from a source and
represent a distance to be monitored.
(ii) Visual detections of marine
mammals or sea turtles within a
mitigation zone shall be communicated
immediately to a watch station for
information dissemination and
appropriate action.
(iii) Mitigation zones for nonimpulsive sound:
(A) The Navy shall ensure that hullmounted mid-frequency active sonar
transmission levels are limited to at
least 6 dB below normal operating levels
if any detected marine mammals or sea
turtles are within 1,000 yd. (914 m) of
the sonar dome (the bow).
(B) The Navy shall ensure that hullmounted mid-frequency active sonar
transmissions are limited to at least 10
dB below the equipment’s normal
operating level if any detected marine
mammals or sea turtles are within 500
yd. (457 m) of the sonar dome.
(C) The Navy shall ensure that hullmounted mid-frequency active sonar
transmissions are ceased if any detected
cetaceans or sea turtles are within 200
yd. (183 m) and pinnipeds are within
100 yd. (90 m) of the sonar dome.
Transmissions shall not resume until
the marine mammal has been observed
exiting the mitigation zone, is thought to
have exited the mitigation zone based
on its course and speed, has not been
detected for 30 minutes, the vessel has
transited more than 2,000 yd. beyond
the location of the last detection, or the
ship concludes that dolphins are
deliberately closing in on the ship to
ride the ship’s bow wave (and there are
no other marine mammal sightings
within the mitigation zone). Active
transmission may resume when
dolphins are bow riding because they
are out of the main transmission axis of
the active sonar while in the shallowwave area of the ship bow.
(D) The Navy shall ensure that highfrequency and non-hull-mounted midfrequency active sonar transmission
levels are ceased if any detected
cetaceans are within 200 yd. (180 m)
and pinnipeds are within 100 yd. (90 m)
of the source. Transmissions shall not
resume until the marine mammal has
been observed exiting the mitigation
zone, is thought to have exited the
mitigation zone based on its course and
speed, the mitigation zone has been
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clear from any additional sightings for a
period of 10 minutes for an aircraftdeployed source, the mitigation zone
has been clear from any additional
sightings for a period of 30 minutes for
a vessel-deployed source, the vessel or
aircraft has repositioned itself more than
400 yd. (370 m) away from the location
of the last sighting, or the vessel
concludes that dolphins are deliberately
closing in to ride the vessel’s bow wave
(and there are no other marine mammal
sightings within the mitigation zone).
(iv) Mitigation zones for explosive
and impulsive sound:
(A) A mitigation zone with a radius of
350 yd. (320 m) shall be established for
explosive signal underwater sonobuoys
using >0.5 to 2.5 lb NEW. Explosive
signal underwater sonobuoys shall not
be deployed if concentrations of floating
vegetation (kelp paddies) are observed
in the mitigation zone (around the
intended deployment location).
Explosive signal underwater sonobuoy
deployment shall cease if a marine
mammal is sighted within the
mitigation zone. Detonations shall
recommence if any one of the following
conditions is met: The animal is
observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, or the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes. Passive acoustic
monitoring shall also be conducted with
Navy assets, such as sonobuoys, already
participating in the activity. These
assets would only detect vocalizing
marine mammals within the frequency
bands monitored by Navy personnel.
Passive acoustic detections would not
provide range or bearing to detected
animals, and therefore cannot provide
locations of these animals. Passive
acoustic detections would be reported to
Lookouts posted in aircraft in order to
increase vigilance of their visual
surveillance.
(B) A mitigation zone with a radius of
200 yd. (180 m) shall be established for
small- and medium-caliber gunnery
exercises with a surface target. The
exercise shall not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Firing shall cease if a
marine mammal is sighted within the
mitigation zone. Firing shall
recommence if any one of the following
conditions is met: The animal is
observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes for a firing aircraft,
the mitigation zone has been clear from
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any additional sightings for a period of
30 minutes for a firing ship, or the
intended target location has been
repositioned more than 400 yd. (370 m)
away from the location of the last
sighting.
(C) A mitigation zone with a radius of
600 yd. (549 m) shall be established for
large-caliber gunnery exercises with a
surface target. The exercise shall not
commence if concentrations of floating
vegetation (kelp paddies) are observed
in the mitigation zone. Firing shall cease
if a marine mammal is sighted within
the mitigation zone. Firing shall
recommence if any one of the following
conditions is met: The animal is
observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, or the mitigation zone has been
clear from any additional sightings for a
period of 30 minutes.
(D) A mitigation zone with a radius of
900 yd. (823 m) shall be established for
missile exercises with up to 250 lb NEW
and a surface target. The exercise shall
not commence if concentrations of
floating vegetation (kelp paddies) are
observed in the mitigation zone. Firing
shall cease if a marine mammal is
sighted within the mitigation zone.
Firing shall recommence if any one of
the following conditions is met: The
animal is observed exiting the
mitigation zone, the animal is thought to
have exited the mitigation zone based
on its course and speed, or the
mitigation zone has been clear from any
additional sightings for a period of 10
minutes or 30 minutes (depending on
aircraft type).
(E) A mitigation zone with a radius of
2,000 yd. (1.8 km) shall be established
for missile exercises with 251 to 500 lb
NEW using a surface target. The exercise
shall not commence if concentrations of
floating vegetation (kelp paddies) are
observed in the mitigation zone. Firing
shall cease if a marine mammal is
sighted within the mitigation zone.
Firing shall recommence if any one of
the following conditions is met: The
animal is observed exiting the
mitigation zone, the animal is thought to
have exited the mitigation zone based
on its course and speed, or the
mitigation zone has been clear from any
additional sightings for a period of 10
minutes or 30 minutes (depending on
aircraft type).
(F) A mitigation zone with a radius of
2,500 yd. (2.3 km) around the intended
impact location for explosive bombs and
1000 yd. (920 m) for non-explosive
bombs shall be established for bombing
exercises. The exercise shall not
commence if concentrations of floating
vegetation (kelp paddies) are observed
PO 00000
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10019
in the mitigation zone. Bombing shall
cease if a marine mammal is sighted
within the mitigation zone. Bombing
shall recommence if any one of the
following conditions is met: The animal
is observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, or the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes.
(G) A mitigation zone with a radius of
2.5 nautical miles shall be established
for sinking exercises. Sinking exercises
shall include aerial observation
beginning 90 minutes before the first
firing, visual observations from vessels
throughout the duration of the exercise,
and both aerial and vessel observation
immediately after any planned or
unplanned breaks in weapons firing of
longer than 2 hours. Prior to conducting
the exercise, the Navy shall review
remotely sensed sea surface temperature
and sea surface height maps to aid in
deciding where to release the target ship
hulk. The Navy shall also monitor using
passive acoustics during the exercise.
Passive acoustic monitoring would be
conducted with Navy assets, such as
passive ships sonar systems or
sonobuoys, already participating in the
activity. These assets would only detect
vocalizing marine mammals within the
frequency bands monitored by Navy
personnel. Passive acoustic detections
would not provide range or bearing to
detected animals, and therefore cannot
provide locations of these animals.
Passive acoustic detections would be
reported to lookouts posted in aircraft
and on vessels in order to increase
vigilance of their visual surveillance.
Lookouts shall also increase observation
vigilance before the use of torpedoes or
unguided ordnance with a NEW of 500
lb. or greater, or if the Beaufort sea state
is a 4 or above. The exercise shall not
commence if concentrations of floating
vegetation (kelp paddies) are observed
in the mitigation zone. The exercise
shall cease if a marine mammal, sea
turtle, or aggregation of jellyfish is
sighted within the mitigation zone. The
exercise shall recommence if any one of
the following conditions is met: The
animal is observed exiting the
mitigation zone, the animal is thought to
have exited the mitigation zone based
on a determination of its course and
speed and the relative motion between
the animal and the source, or the
mitigation zone has been clear from any
additional sightings for a period of 30
minutes. Upon sinking the vessel, the
Navy shall conduct post-exercise visual
surveillance of the mitigation zone for 2
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hours (or until sunset, whichever comes
first).
(H) A mitigation zone of 70 yd. (46 m)
shall be established for all explosive
large-caliber gunnery exercises
conducted from a ship. The exercise
shall not commence if concentrations of
floating vegetation (kelp paddies) are
observed in the mitigation zone. Firing
shall cease if a marine mammal is
sighted within the mitigation zone.
Firing shall recommence if any one of
the following conditions is met: The
animal is observed exiting the
mitigation zone, the animal is thought to
have exited the mitigation zone based
on its course and speed, the mitigation
zone has been clear from any additional
sightings for a period of 30 minutes, or
the vessel has repositioned itself more
than 140 yd. (128 m) away from the
location of the last sighting.
(v) Mitigation zones for vessels and
in-water devices:
(A) A mitigation zone of 500 yd. (460
m) for observed whales and 200 yd (183
m) for all other marine mammals
(except bow riding dolphins) shall be
established for all vessel movement
during training activities, providing it is
safe to do so.
(B) A mitigation zone of 250 yd. (229
m) shall be established for all towed inwater devices, providing it is safe to do
so.
(vi) Mitigation zones for nonexplosive practice munitions:
(A) A mitigation zone of 200 yd. (180
m) shall be established for small,
medium, and large caliber gunnery
exercises using a surface target. The
exercise shall not commence if
concentrations of floating vegetation
(kelp paddies) are observed in the
mitigation zone. Firing shall cease if a
marine mammal is sighted within the
mitigation zone. Firing shall
recommence if any one of the following
conditions is met: The animal is
observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes for a firing aircraft,
the mitigation zone has been clear from
any additional sightings for a period of
30 minutes for a firing ship, or the
intended target location has been
repositioned more than 400 yd. (370 m)
away from the location of the last
sighting.
(B) A mitigation zone of 1,000 yd.
(920 m) shall be established for bombing
exercises. Bombing shall cease if a
marine mammal is sighted within the
mitigation zone. The exercise shall not
commence if concentrations of floating
vegetation (kelp paddies) are observed
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in the mitigation zone. Bombing shall
recommence if any one of the following
conditions is met: The animal is
observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, or the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes.
(C) A mitigation zone of 900 yd. (823
m) shall be established for missile
exercises (including rockets) using a
surface target. The exercise shall not
commence if concentrations of floating
vegetation (kelp paddies) are observed
in the mitigation zone. Firing shall cease
if a marine mammal is sighted within
the mitigation zone. Firing shall
recommence if any one of the following
conditions is met: The animal is
observed exiting the mitigation zone,
the animal is thought to have exited the
mitigation zone based on its course and
speed, or the mitigation zone has been
clear from any additional sightings for a
period of 10 minutes or 30 minutes
(depending on aircraft type).
(3) Stranding response plan. (i) The
Navy shall abide by the letter of the
‘‘Stranding Response Plan for Major
Navy Training Exercises in the GOA
TMAA Study Area,’’ to include the
following measures:
(A) Shutdown procedures. When an
Uncommon Stranding Event (USE)
occurs during a Major Training Exercise
(MTE) in the Study Area, the Navy shall
implement the procedures described
below:
(1) The Navy shall implement a
shutdown when advised by a NMFS
Office of Protected Resources
Headquarters Senior Official designated
in the GOA TMAA Study Area
Stranding Communication Protocol that
a USE involving live animals has been
identified and that at least one live
animal is located in the water. NMFS
and the Navy shall maintain a dialogue,
as needed, regarding the identification
of the USE and the potential need to
implement shutdown procedures.
(2) Any shutdown in a given area
shall remain in effect in that area until
NMFS advises the Navy that the
subject(s) of the USE at that area die or
are euthanized, or that all live animals
involved in the USE at that area have
left the area (either of their own volition
or herded).
(3) If the Navy finds an injured or
dead animal floating at sea during an
MTE, the Navy shall notify NMFS
immediately or as soon as operational
security considerations allow. The Navy
shall provide NMFS with species or
description of the animal(s), the
condition of the animal(s), including
carcass condition if the animal(s) is/are
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dead, location, time of first discovery,
observed behavior (if alive), and photo
or video (if available). Based on the
information provided, NFMS shall
determine if, and advise the Navy
whether a modified shutdown is
appropriate on a case-by-case basis.
(4) In the event, following a USE, that
qualified individuals are attempting to
herd animals back out to the open ocean
and animals are not willing to leave, or
animals are seen repeatedly heading for
the open ocean but turning back to
shore, NMFS and the Navy shall
coordinate (including an investigation
of other potential anthropogenic
stressors in the area) to determine if the
proximity of mid-frequency active sonar
training activities or explosive
detonations, though farther than 14
nautical miles from the distressed
animal(s), is likely contributing to the
animals’ refusal to return to the open
water. If so, NMFS and the Navy shall
further coordinate to determine what
measures are necessary to improve the
probability that the animals will return
to open water and implement those
measures as appropriate.
(B) Within 72 hours of NMFS
notifying the Navy of the presence of a
USE, the Navy shall provide available
information to NMFS (per the GOA
TMAA Study Area Communication
Protocol) regarding the location, number
and types of acoustic/explosive sources,
direction and speed of units using midfrequency active sonar, and marine
mammal sightings information
associated with training activities
occurring within 80 nautical miles (148
km) and 72 hours prior to the USE
event. Information not initially available
regarding the 80-nautical miles (148–
km), 72–hour period prior to the event
shall be provided as soon as it becomes
available. The Navy shall provide NMFS
investigative teams with additional
relevant unclassified information as
requested, if available.
(ii) [Reserved]
(b) [Reserved]
§ 218.155 Requirements for monitoring
and reporting.
(a) The Holder of the Authorization
must notify NMFS immediately (or as
soon as operational security
considerations allow) if the specified
activity identified in § 218.150 is
thought to have resulted in the mortality
or injury of any marine mammals, or in
any take of marine mammals not
identified in § 218.152(c).
(b) The Holder of the LOA must
conduct all monitoring and required
reporting under the LOA, including
abiding by the GOA TMAA monitoring
plan.
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(c) General notification of injured or
dead marine mammals. Navy personnel
shall ensure that NMFS (regional
stranding coordinator) is notified
immediately (or as soon as operational
security considerations allow) if an
injured or dead marine mammal is
found during or shortly after, and in the
vicinity of, a Navy training activity
utilizing mid- or high-frequency active
sonar, or underwater explosive
detonations. The Navy shall provide
NMFS with species or description of the
animal(s), the condition of the animal(s)
(including carcass condition if the
animal is dead), location, time of first
discovery, observed behaviors (if alive),
and photo or video (if available). In the
event that an injured, stranded, or dead
marine mammal is found by the Navy
that is not in the vicinity of, or during
or shortly after, MFAS, HFAS, or
underwater explosive detonations, the
Navy shall report the same information
as listed above as soon as operationally
feasible and clearance procedures allow.
(d) General notification of ship strike.
In the event of a ship strike by any Navy
vessel, at any time or place, the Navy
shall do the following:
(1) Immediately report to NMFS the
species identification (if known),
location (lat/long) of the animal (or the
strike if the animal has disappeared),
and whether the animal is alive or dead
(or unknown), and the time of the strike.
(2) Report to NMFS as soon as
operationally feasible the size and
length of animal, an estimate of the
injury status (ex., dead, injured but
alive, injured and moving, unknown,
etc.), vessel class/type and operational
status.
(3) Report to NMFS the vessel length,
speed, and heading as soon as feasible.
(4) Provide NMFS a photo or video, if
equipment is available.
(5) Within 2 weeks of the strike,
provide NMFS with a detailed
description of the specific actions of the
vessel in the 30–minute timeframe
immediately preceding the strike,
during the event, and immediately after
the strike (e.g., the speed and changes in
speed, the direction and changes in
direction, other maneuvers, sonar use,
etc., if not classified); a narrative
description of marine mammal sightings
during the event and immediately after,
and any information as to sightings
prior to the strike, if available; and use
established Navy shipboard procedures
to make a camera available to attempt to
capture photographs following a ship
strike.
(e) Communication plan. The Navy
and NMFS shall develop a
communication plan that will include
all of the communication protocols
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(phone trees, etc.) and associated
contact information required for NMFS
and the Navy to carry out the necessary
expeditious communication required in
the event of a stranding or ship strike,
including information described in the
proposed notification measures above.
(f) Annual GOA TMAA monitoring
report. The Navy shall submit an annual
report of the GOA TMAA monitoring
describing the implementation and
results from the previous calendar year.
Data collection methods shall be
standardized across range complexes
and study areas to allow for comparison
in different geographic locations.
Although additional information will be
gathered, the protected species
observers collecting marine mammal
data pursuant to the GOA TMAA
monitoring plan shall, at a minimum,
provide the same marine mammal
observation data required in § 218.155.
The report shall be submitted either 90
days after the calendar year, or 90 days
after the conclusion of the monitoring
year to be determined by the Adaptive
Management process. The GOA TMAA
Monitoring Report may be provided to
NMFS within a larger report that
includes the required Monitoring Plan
reports from multiple range complexes
and study areas (the multi-Range
Complex Annual Monitoring Report).
Such a report would describe progress
of knowledge made with respect to
monitoring plan study questions across
all Navy ranges associated with the
Integrated Comprehensive Monitoring
Program. Similar study questions shall
be treated together so that progress on
each topic shall be summarized across
all Navy ranges. The report need not
include analyses and content that does
not provide direct assessment of
cumulative progress on the monitoring
plan study questions.
(g) Annual GOA TMAA exercise
reports. Each year, the Navy shall
submit a preliminary report detailing
the status of authorized sound sources
within 21 days after the anniversary of
the date of issuance of the LOA. Each
year, the Navy shall submit a detailed
report within 3 months after the
anniversary of the date of issuance of
the LOA. The annual report shall
contain information on Major Training
Exercises (MTEs), Sinking Exercise
(SINKEX) events, and a summary of all
sound sources used, as described in
paragraph (g)(3) of this section. The
analysis in the detailed report shall be
based on the accumulation of data from
the current year’s report and data
collected from previous the report. The
detailed reports shall contain
information identified in paragraphs
(g)(1) through (4) of this section.
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10021
(1) MFAS/HFAS Major Training
Exercises—This section shall contain
the following information for Major
Training Exercises conducted in the
GOA TMAA:
(i) Exercise Information (for each
MTE):
(A) Exercise designator.
(B) Date that exercise began and
ended.
(C) Location.
(D) Number and types of active
sources used in the exercise.
(E) Number and types of passive
acoustic sources used in exercise.
(F) Number and types of vessels,
aircraft, etc., participating in exercise.
(G) Total hours of observation by
lookouts.
(H) Total hours of all active sonar
source operation.
(I) Total hours of each active sonar
source bin.
(J) Wave height (high, low, and
average during exercise).
(ii) Individual marine mammal
sighting information for each sighting in
each exercise when mitigation occurred:
(A) Date/Time/Location of sighting.
(B) Species (if not possible, indication
of whale/dolphin/pinniped).
(C) Number of individuals.
(D) Initial Detection Sensor.
(E) Indication of specific type of
platform observation made from
(including, for example, what type of
surface vessel or testing platform).
(F) Length of time observers
maintained visual contact with marine
mammal.
(G) Sea state.
(H) Visibility.
(I) Sound source in use at the time of
sighting.
(J) Indication of whether animal is
<200 yd, 200 to 500 yd, 500 to 1,000 yd,
1,000 to 2,000 yd, or >2,000 yd from
sonar source.
(K) Mitigation implementation.
Whether operation of sonar sensor was
delayed, or sonar was powered or shut
down, and how long the delay was.
(L) If source in use is hull-mounted,
true bearing of animal from ship, true
direction of ship’s travel, and estimation
of animal’s motion relative to ship
(opening, closing, parallel).
(M) Observed behavior. Lookouts
shall report, in plain language and
without trying to categorize in any way,
the observed behavior of the animals
(such as animal closing to bow ride,
paralleling course/speed, floating on
surface and not swimming, etc.) and if
any calves present.
(iii) An evaluation (based on data
gathered during all of the MTEs) of the
effectiveness of mitigation measures
designed to minimize the received level
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to which marine mammals may be
exposed. This evaluation shall identify
the specific observations that support
any conclusions the Navy reaches about
the effectiveness of the mitigation.
(2) SINKEXs. This section shall
include the following information for
each SINKEX completed that year:
(i) Exercise information (gathered for
each SINKEX):
(A) Location.
(B) Date and time exercise began and
ended.
(C) Total hours of observation by
lookouts before, during, and after
exercise.
(D) Total number and types of
explosive source bins detonated.
(E) Number and types of passive
acoustic sources used in exercise.
(F) Total hours of passive acoustic
search time.
(G) Number and types of vessels,
aircraft, etc., participating in exercise.
(H) Wave height in feet (high, low,
and average during exercise).
(I) Narrative description of sensors
and platforms utilized for marine
mammal detection and timeline
illustrating how marine mammal
detection was conducted.
(ii) Individual marine mammal
observation (by Navy lookouts)
information (gathered for each marine
mammal sighting) for each sighting in
each exercise that required mitigation to
be implemented:
(A) Date/Time/Location of sighting.
(B) Species (if not possible, indicate
whale, dolphin, or pinniped).
(C) Number of individuals.
(D) Initial detection sensor.
(E) Length of time observers
maintained visual contact with marine
mammal.
(F) Sea state.
(G) Visibility.
(H) Whether sighting was before,
during, or after detonations/exercise,
and how many minutes before or after.
(I) Distance of marine mammal from
actual detonations (or target spot if not
yet detonated).
(J) Observed behavior. Lookouts shall
report, in plain language and without
trying to categorize in any way, the
observed behavior of the animal(s) (such
as animal closing to bow ride,
paralleling course/speed, floating on
surface and not swimming etc.),
including speed and direction and if
any calves present.
(K) Resulting mitigation
implementation. Indicate whether
explosive detonations were delayed,
ceased, modified, or not modified due to
marine mammal presence and for how
long.
(L) If observation occurs while
explosives are detonating in the water,
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indicate munition type in use at time of
marine mammal detection.
(3) Summary of sources used.
(i) This section shall include the
following information summarized from
the authorized sound sources used in all
training events:
(A) Total annual hours or quantity
(per the LOA) of each bin of sonar or
other non-impulsive source;
(B) Total annual number of each type
of explosive exercises (of those
identified as part of the ‘‘Specified
Activity’’ in this proposed rule) and
total annual expended/detonated
rounds (missiles, bombs, sonobuoys,
etc.) for each explosive bin.
(4) Geographic information
presentation. The reports shall present
an annual (and seasonal, where
practical) depiction of training exercises
and testing bin usage geographically
across the Study Area.
(g) Sonar exercise notification. The
Navy shall submit to NMFS (contact as
specified in the LOA) an electronic
report within fifteen calendar days after
the completion of any major training
exercise indicating:
(i) Location of the exercise.
(ii) Beginning and end dates of the
exercise.
(iii) Type of exercise.
(h) Five-year close-out exercise report.
This report shall be included as part of
the 2021 annual exercise report. This
report shall provide the annual totals for
each sound source bin with a
comparison to the annual allowance and
the 5-year total for each sound source
bin with a comparison to the 5-year
allowance. Additionally, if there were
any changes to the sound source
allowance, this report shall include a
discussion of why the change was made
and include the analysis to support how
the change did or did not result in a
change in the SEIS and final rule
determinations. The report shall be
submitted 3 months after the expiration
of this subpart. NMFS shall submit
comments on the draft close-out report,
if any, within 3 months of receipt. The
report shall be considered final after the
Navy has addressed NMFS’ comments,
or 3 months after the submittal of the
draft if NMFS does not provide
comments.
§ 218.156 Applications for letters of
authorization (LOA).
To incidentally take marine mammals
pursuant to the regulations in this
subpart, the U.S. citizen (as defined by
§ 216.106 of this chapter) conducting
the activity identified in § 218.150(c)
(the U.S. Navy) must apply for and
obtain either an initial LOA in
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Fmt 4701
Sfmt 4702
accordance with § 218.157 or a renewal
under § 218.158.
§ 218.157
Letters of authorization (LOA).
(a) An LOA, unless suspended or
revoked, shall be valid for a period of
time not to exceed the period of validity
of this subpart.
(b) Each LOA shall set forth:
(1) Permissible methods of incidental
taking;
(2) Means of effecting the least
practicable adverse impact on the
species, its habitat, and on the
availability of the species for
subsistence uses (i.e., mitigation); and
(3) Requirements for mitigation,
monitoring and reporting.
(c) Issuance and renewal of the LOA
shall be based on a determination that
the total number of marine mammals
taken by the activity as a whole shall
have no more than a negligible impact
on the affected species or stock of
marine mammal(s).
§ 218.158 Renewals and modifications of
letters of authorization (LOA) and adaptive
management.
(a) A letter of authorization issued
under §§ 216.106 and 218.157 of this
chapter for the activity identified in
§ 218.150(c) shall be renewed or
modified upon request of the applicant,
provided that:
(1) The proposed specified activity
and mitigation, monitoring, and
reporting measures, as well as the
anticipated impacts, are the same as
those described and analyzed for these
regulations (excluding changes made
pursuant to the adaptive management
provision of this chapter), and;
(2) NMFS determines that the
mitigation, monitoring, and reporting
measures required by the previous LOA
under these regulations were
implemented.
(b) For LOA modification or renewal
requests by the applicant that include
changes to the activity or the mitigation,
monitoring, or reporting (excluding
changes made pursuant to the adaptive
management provision of this chapter)
that do not change the findings made for
the regulations or result in no more than
a minor change in the total estimated
number of takes (or distribution by
species or years), NMFS may publish a
notice of proposed LOA in the Federal
Register, including the associated
analysis illustrating the change, and
solicit public comment before issuing
the LOA.
(c) A LOA issued under § 216.106 and
§ 218.157 of this chapter for the activity
identified in § 218.154 of this chapter
may be modified by NMFS under the
following circumstances:
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(1) Adaptive management. NMFS may
modify and augment the existing
mitigation, monitoring, or reporting
measures (after consulting with the
Navy regarding the practicability of the
modifications) if doing so creates a
reasonable likelihood of more
effectively accomplishing the goals of
the mitigation and monitoring.
(i) Possible sources of data that could
contribute to the decision to modify the
mitigation, monitoring, and reporting
measures in an LOA:
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20:44 Feb 25, 2016
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(A) Results from Navy’s monitoring
from the previous year(s);
(B) Results from other marine
mammal and/or sound research or
studies; or
(C) Any information that reveals
marine mammals may have been taken
in a manner, extent, or number not
authorized by these regulations or
subsequent LOA.
(ii) If, through adaptive management,
the modifications to the mitigation,
monitoring, or reporting measures are
substantial, NMFS would publish a
PO 00000
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Fmt 4701
Sfmt 9990
10023
notice of proposed LOA in the Federal
Register and solicit public comment.
(2) Emergencies. If NMFS determines
that an emergency exists that poses a
significant risk to the well-being of the
species or stocks of marine mammals
specified in § 218.152(c), an LOA may
be modified without prior notification
and an opportunity for public comment.
Notification would be published in the
Federal Register within 30 days of the
action.
[FR Doc. 2016–03622 Filed 2–25–16; 8:45 am]
BILLING CODE 3510–22–P
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Agencies
[Federal Register Volume 81, Number 38 (Friday, February 26, 2016)]
[Proposed Rules]
[Pages 9949-10023]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-03622]
[[Page 9949]]
Vol. 81
Friday,
No. 38
February 26, 2016
Part II
Department of Commerce
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National Oceanic and Atmospheric Administration
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50 CFR Part 218
Takes of Marine Mammals Incidental to Specified Activities; U.S. Navy
Training Activities in the Gulf of Alaska Temporary Maritime Activities
Area; Proposed Rule
Federal Register / Vol. 81 , No. 38 / Friday, February 26, 2016 /
Proposed Rules
[[Page 9950]]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
50 CFR Part 218
[Docket No. 141125997-6058-01]
RIN 0648-BE67
Takes of Marine Mammals Incidental to Specified Activities; U.S.
Navy Training Activities in the Gulf of Alaska Temporary Maritime
Activities Area
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Proposed rule; request for comments and information.
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SUMMARY: NMFS has received a request from the U.S. Navy (Navy) for
authorization to take marine mammals incidental to the training
activities conducted in the Gulf of Alaska (GOA) Temporary Maritime
Activities Area (TMAA) Study Area (hereafter referred to the Study
Area) from May 2016 through May 2021. Pursuant to the Marine Mammal
Protection Act (MMPA), NMFS is requesting comments on its proposal to
issue regulations and subsequent Letter of Authorization (LOA) to the
Navy to incidentally harass marine mammals.
DATES: Comments and information must be received no later than March
28, 2016.
ADDRESSES: You may submit comments, identified by NOAA-NMFS-2016-0008,
by any of the following methods:
Electronic submissions: submit all electronic public
comments via the Federal eRulemaking Portal, Go to www.regulations.gov/#!docketDetail;D=NOAA-NMFS-2016-0008, click the ``Comment Now!'' icon,
complete the required fields, and enter or attach your comments.
Mail: Submit comments to Jolie Harrison, Chief, Permits
and Conservation Division, Office of Protected Resources, National
Marine Fisheries Service, 1315 East-West Highway, Silver Spring, MD
20910-3225.
Fax: (301) 713-0376; Attn: Jolie Harrison.
Instructions: Comments sent by any other method, to any other
address or individual, or received after the end of the comment period,
may not be considered by NMFS. All comments received are a part of the
public record and will generally be posted for public viewing on
www.regulations.gov without change. All personal identifying
information (e.g., name, address, etc.), confidential business
information, or otherwise sensitive information submitted voluntarily
by the sender will be publicly accessible. NMFS will accept anonymous
comments (enter ``N/A'' in the required fields if you wish to remain
anonymous). Attachments to electronic comments will be accepted in
Microsoft Word, Excel, or Adobe PDF file formats only.
FOR FURTHER INFORMATION CONTACT: John Fiorentino, Office of Protected
Resources, NMFS, (301) 427-8477.
SUPPLEMENTARY INFORMATION:
Availability
A copy of the Navy's LOA application, which contains a list of the
references used in this proposed rule, may be obtained by visiting the
internet at: https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm. The Navy is preparing a Supplemental Environmental Impact
Statement (SEIS)/Overseas EIS (OEIS) for the GOA TMAA Study Area to
evaluate all components of the proposed training activities. The Navy
previously analyzed training activities in the Study Area in the 2011
GOA Navy Training Activities FEIS (GOA FEIS/OEIS) (U.S. Department of
the Navy, 2011a). The GOA Draft Supplemental EIS (DSEIS)/OEIS was
released to the public on August 23, 2014, for review until October 22,
2014. The Navy is the lead agency for the GOA SEIS/OEIS, and NMFS is a
cooperating agency pursuant to 40 CFR 1501.6 and 1508.5. The GOA DSEIS/
OEIS, which also contains a list of the references used in this
proposed rule, may be viewed at: https://www.goaeis.com. Documents cited
in this notice may also be viewed, by appointment, during regular
business hours, at the aforementioned address.
Background
Sections 101(a)(5)(A) and (D) of the MMPA (16 U.S.C. 1361 et seq.)
direct the Secretary of Commerce to allow, upon request, the
incidental, but not intentional, taking of small numbers of marine
mammals by U.S. citizens who engage in a specified activity (other than
commercial fishing) within a specified geographical region if certain
findings are made and either regulations are issued or, if the taking
is limited to harassment, a notice of a proposed authorization is
provided to the public for review.
Authorization for incidental takings shall be granted if NMFS finds
that the taking will have a negligible impact on the species or
stock(s), will not have an unmitigable adverse impact on the
availability of the species or stock(s) for subsistence uses (where
relevant), and if the permissible methods of taking and requirements
pertaining to the mitigation, monitoring, and reporting of such takings
are set forth. NMFS has defined ``negligible impact'' in 50 CFR 216.103
as ``an impact resulting from the specified activity that cannot be
reasonably expected to, and is not reasonably likely to, adversely
affect the species or stock through effects on annual rates of
recruitment or survival.''
The National Defense Authorization Act of 2004 (NDAA) (Pub. L. 108-
136) removed the ``small numbers'' and ``specified geographical
region'' limitations indicated above and amended the definition of
``harassment'' as applies to a ``military readiness activity'' to read
as follows (section 3(18)(B) of the MMPA, 16 U.S.C. 1362(18)(B)): ``(i)
any act that injures or has the significant potential to injure a
marine mammal or marine mammal stock in the wild'' [Level A
Harassment]; or ``(ii) any act that disturbs or is likely to disturb a
marine mammal or marine mammal stock in the wild by causing disruption
of natural behavioral patterns, including, but not limited to,
migration, surfacing, nursing, breeding, feeding, or sheltering, to a
point where such behavioral patterns are abandoned or significantly
altered'' [Level B Harassment].
Summary of Request
On July 28, 2014, NMFS received an application from the Navy
requesting a LOA for the take of 19 species of marine mammals
incidental to Navy training activities to be conducted in the Study
Area over 5 years. On October 14, 2014, the Navy submitted a revised
LOA application to reflect minor changes in the number and types of
training activities. To address minor inconsistencies with the DSEIS,
the Navy submitted a final revision to the LOA application (hereafter
referred to as the LOA application) on January 21, 2015.
The Navy is requesting a 5-year LOA for training activities to be
conducted from 2016 through 2021. The Study Area is a polygon roughly
the shape of a 300 nm by 150 nm rectangle oriented northwest to
southeast in the long direction, located south of Prince William Sound
and east of Kodiak Island, Alaska (see Figure 1-1 of the LOA
application for a map of the Study Area). The activities conducted
within the Study Area are classified as military readiness activities.
The Navy states that these activities may expose some of the marine
mammals present within the Study Area to sound from underwater
[[Page 9951]]
acoustic sources and explosives. The Navy requests authorization to
take 19 marine mammal species by Level B (behavioral) harassment; one
of those marine mammal species (Dall's porpoise) may be taken by Level
A (injury) harassment. The Navy is not requesting mortality takes for
any species.
The LOA application and the GOA DSEIS/OEIS contain acoustic
thresholds that, in some instances, represent changes from what NMFS
has used to evaluate the Navy's activities for previous authorizations.
The revised thresholds, which the Navy developed in coordination with
NMFS, are based on the evaluation and inclusion of new information from
recent scientific studies; a detailed explanation of how they were
derived is provided in the GOA DSEIS/OEIS Criteria and Thresholds for
U.S. Navy Acoustic and Explosive Effects Analysis Technical Report
(available at https://www.goaeis.com). The revised thresholds are
adopted for this proposed rulemaking.
NOAA is currently in the process of developing Acoustic Guidance on
thresholds for onset of auditory impacts from exposure to sound, which
will be used to support assessments of the effects of anthropogenic
sound on marine mammals. To develop this Guidance, NOAA is compiling,
interpreting, and synthesizing the best information currently available
on the effects of anthropogenic sound on marine mammals, and is
committed to finalizing the Guidance through a systematic, transparent
process that involves internal review, external peer review, and public
comment.
In December 2013, NOAA released for public comment a ``Draft
Guidance for Assessing the Effects of Anthropogenic Sound on Marine
Mammals: Acoustic Threshold Levels for Onset of Permanent and Temporary
Threshold Shifts'' (78 FR 78822) (the term ``threshold shift'' refers
to noise-induced hearing loss). The Draft Guidance was generally
consistent with the Navy's Permanent Threshold Shifts/Temporary
Threshold Shifts (PTS/TTS) criteria used in the GOA DSEIS/OEIS and
detailed within Finneran and Jenkins (2012). Prior to the finalization
of this guidance by NOAA, the Navy suggested revisions to the criteria
(e.g., auditory weighting functions and PTS/TTS thresholds) based on a
number of studies available since the Navy's Phase 2 modeling (the
acoustic effects modeling currently employed by the Navy for training
and testing activities), including Finneran et al. (2005), Finneran et
al. (2010), Finneran and Schlundt (2013), Kastelein et al. (2012a),
Kastelein et al. (2012b), Kastelein et al. (2014a), Kastelein et al.
(2014b), Popov et al. (2013), and Popov et al. (2011). In January 2015,
the Navy submitted a draft proposal (Finneran 2015) to NOAA staff for
their consideration.
Finneran (2015) proposed new weighting functions and thresholds for
predicting PTS/TTS in marine mammals. The methodologies presented
within this paper build upon the methodologies used to develop the
criteria applied within the Navy's GOA DSEIS/OEIS (Finneran and
Jenkins, 2012) and incorporate relevant auditory research made
available since 2012. While Finneran and Jenkins (2012) presented a
conservative approach to development of auditory weighting functions
where data was limited, Finneran (2015) synthesizes a wide range of
auditory data, including newly available studies, to predict refined
auditory weighting functions and corresponding TTS thresholds across
the complete hearing ranges of functional hearing groups.
During the development process of NOAA's Draft Guidance, NOAA
incorporated Finneran (2015) into its Draft Guidance. As a result, the
Navy's proposal (Finneran, 2015) was submitted for peer review by
external subject matter experts, in accordance with the process
previously conducted for NOAA's Draft Guidance. Peer review comments
were received by NOAA in April 2015. NOAA subsequently developed a Peer
Review Report, which was published on its Web site on July 31, 2015.
The published report documents the Navy's proposal (Finneran, 2015)
that underwent peer review, the peer-review comments, and NOAA's
responses to those comments. NOAA then incorporated this information
into revised Draft Guidance which was published in the Federal Register
for public review and comment (80 FR 45642) on July 31, 2015. The
auditory weighting functions and PTS/TTS thresholds provided in that
revised Draft Guidance will not be adopted by NOAA or applied to
applicants until Final Guidance is issued. At the time of this proposed
rulemaking, Final Guidance has not been issued. Therefore, the Navy has
not adopted these proposed criteria in its GOA DSEIS/OEIS. However, the
underlying science contained within Finneran (2015) has been addressed
qualitatively within the applicable sections of the GOA DSEIS/OEIS and
this rulemaking.
If the proposed criteria in Finneran (2015) were adopted by NOAA,
incorporated into its Final Guidance, and applied to the Navy in the
future, predicted numbers of PTS/TTS would change for most functional
hearing groups. However, because Finneran (2015) relies on much of the
same data as the auditory criteria presented in the Navy's GOA DSEIS/
OEIS, these changes would not be substantial, and in most cases would
result in a reduction in the predicted impacts. Predicted PTS/TTS would
be reduced over much to all of their hearing range for low-frequency
cetaceans and phocids. Predicted PTS/TTS for mid-frequency and high-
frequency cetaceans would be reduced for sources with frequencies below
about 3.5 kHz and remain relatively unchanged for sounds above this
frequency. Predicted auditory effects on otariids would increase for
frequencies between about 1 kHz and 20 kHz and decrease for frequencies
above and below these points, although otariids remain the marine
mammals with the least sensitivity to potential PTS/TTS. Overall,
predicted auditory effects within this rulemaking would not change
significantly.
In summary, NOAA's continuing evaluation of all available science
for the Acoustic Guidance could result in changes to the acoustic
criteria used to model the Navy's activities for this rulemaking, and,
consequently, the enumerations of ``take'' estimates. However, at this
time, the results of prior Navy modeling described in this notice
represent the best available estimate of the number and type of take
that may result from the Navy's use of acoustic sources in the GOA
Study Area. Further, consideration of the revised Draft Guidance and
information contained in Finneran (2015) does not alter our assessment
of the likely responses of marine mammals to acoustic sources employed
by Navy in the GOA Study Area, or the likely fitness consequences of
those responses. Finally, while acoustic criteria may also inform
mitigation and monitoring decisions, this rulemaking requires a robust
adaptive management program that regularly addresses new information
and allows for modification of mitigation and/or monitoring measures as
appropriate.
Background of Request
The Navy's mission is to organize, train, equip, and maintain
combat-ready naval forces capable of winning wars, deterring
aggression, and maintaining freedom of the seas. This mission is
mandated by federal law (10 U.S.C. 5062), which ensures the readiness
of
[[Page 9952]]
the naval forces of the United States.\1\ The Navy executes this
responsibility by establishing and executing training programs,
including at-sea training and exercises, and ensuring naval forces have
access to the ranges, operating areas (OPAREAs), and airspace needed to
develop and maintain skills for conducting naval activities.
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\1\ Title 10, Section 5062 of the U.S.C.
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The Navy proposes to continue conducting training activities within
the Study Area, which have been ongoing since the 1990s. The tempo and
types of training activities have fluctuated because of the
introduction of new technologies, the evolving nature of international
events, advances in war fighting doctrine and procedures, and force
structure (organization of ships, submarines, aircraft, weapons, and
personnel) changes. Such developments influence the frequency,
duration, intensity, and location of required training activities.
The Navy's LOA request covers training activities that would occur
for a 5-year period following the expiration of the current MMPA
authorization for the GOA TMAA, which expires in 2016.
Description of the Specified Activity
The Navy is requesting authorization to take marine mammals
incidental to conducting training activities. The Navy has determined
that sonar use and underwater detonations are the stressors most likely
to result in impacts on marine mammals that could rise to the level of
harassment. Detailed descriptions of these activities are provided in
the DSEIS/OEIS and in the LOA application (https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm) and are summarized here.
Overview of Training Activities
The Navy routinely trains in the Study Area in preparation for
national defense missions. Training activities and exercises covered in
the Navy's LOA request are briefly described below, and in more detail
within chapter 2 of the GOA DSEIS/OEIS. Each military training activity
described meets a requirement that can be traced ultimately to
requirements set forth by the National Command Authority.\2\
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\2\ ``National Command Authority'' is a term used by the United
States military and government to refer to the ultimate lawful
source of military orders. The term refers collectively to the
President of the United States (as commander-in-chief) and the
United States Secretary of Defense.
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The Navy categorizes training activities into eight functional
warfare areas called primary mission areas: anti-air warfare;
amphibious warfare; strike warfare; anti-surface warfare (ASUW); anti-
submarine warfare (ASW); electronic warfare; mine warfare (MIW); and
naval special warfare (NSW). Most training activities are categorized
under one of these primary mission areas; those activities that do not
fall within one of these areas are in a separate ``other'' category.
Each warfare community (surface, subsurface, aviation, and special
warfare) may train within some or all of these primary mission areas.
However, not all primary mission areas are conducted within the Study
Area.
The Navy described and analyzed the effects of its training
activities within the GOA DSEIS/OEIS. In its assessment, the Navy
concluded that of the activities conducted within the Study Area, sonar
use and underwater detonations were the stressors resulting in impacts
on marine mammals that could rise to the level of harassment as defined
under the MMPA. Therefore, the LOA application provides the Navy's
assessment of potential effects from these stressors. The specific
acoustic sources used in the LOA application are contained in the GOA
DSEIS/OEIS and are presented in the following sections based on the
primary mission areas.
Anti-Surface Warfare (ASUW)
The mission of ASUW is to defend against enemy ships or boats. In
the conduct of ASUW, aircraft use cannons, air-launched cruise missiles
or other precision-guided munitions; ships employ torpedoes, naval
guns, and surface-to-surface (S-S) missiles; and submarines attack
surface ships using torpedoes or submarine-launched, anti-ship cruise
missiles.
Anti-surface warfare training in the Study Area includes S-S
gunnery and missile exercises (GUNEX and MISSILEX) and air-to-surface
(A-S) bombing exercises (BOMBEX), GUNEX, and MISSILEX. Also included in
this mission area is a sinking exercise that may include S-S and A-S
components.
Anti-Submarine Warfare (ASW)
The mission of ASW is to locate, neutralize, and defeat hostile
submarine threats to surface forces. ASW is based on the principle of a
layered defense of surveillance and attack aircraft, ships, and
submarines all searching for hostile submarines. These forces operate
together or independently to gain early warning and detection, and to
localize, track, target, and attack hostile submarine threats.
Anti-submarine warfare training addresses basic skills such as
detection and classification of submarines, distinguishing between
sounds made by enemy submarines and those of friendly submarines,
ships, and marine life. ASW training evaluates the ability of fleet
assets to use systems, for example, active and passive sonar and
torpedo systems to counter hostile submarine threats. More advanced,
integrated ASW training exercises are conducted in coordinated, at-sea
training events involving submarines, ships, and aircraft. This
training integrates the full spectrum of ASW from detecting and
tracking a submarine to attacking a target using simulated weapons.
Description of Sonar, Ordnance, Targets, and Other Systems
The Navy uses a variety of sensors, platforms, weapons, and other
devices to meet its mission. Training with these systems and devices
may introduce acoustic (sound) energy into the environment. The Navy's
current LOA application describes underwater sound as one of two types:
impulsive and non-impulsive. Sonar and similar sound producing systems
are categorized as non-impulsive sound sources. Underwater detonations
of explosives and other percussive events are impulsive sounds.
Sonar and Other Active Acoustic Sources
Modern sonar technology includes a variety of sonar sensor and
processing systems. In concept, the simplest active sonar emits sound
waves, or ``pings,'' sent out in multiple directions, and the sound
waves then reflect off of the target object in multiple directions. The
sonar source calculates the time it takes for the reflected sound waves
to return; this calculation determines the distance to the target
object. More sophisticated active sonar systems emit a ping and then
rapidly scan or listen to the sound waves in a specific area. This
provides both distance to the target and directional information. Even
more advanced sonar systems use multiple receivers to listen to echoes
from several directions simultaneously and provide efficient detection
of both direction and distance. Active sonar is rarely used
continuously throughout the listed activities. In general, when sonar
is in use, the sonar `pings' occur at intervals, referred to as a duty
cycle, and the signals themselves are very short in duration. For
example, sonar that emits a 1-second ping every 10 seconds has a 10
percent duty cycle. The Navy's largest hull-mounted mid-frequency sonar
source typically emits a 1-second ping every 50 seconds representing a
2 percent duty cycle. The Navy utilizes sonar systems and other
acoustic sensors in support of a variety of
[[Page 9953]]
mission requirements. Primary uses include the detection of and defense
against submarines (ASW) and mines (MIW); safe navigation and effective
communications; use of unmanned undersea vehicles; and oceanographic
surveys. Sources of sonar and other active acoustic sources include
surface ship sonar, sonobuoys, torpedoes, and unmanned underwater
vehicles.
Ordnance and Munitions
Most ordnance and munitions used during training events fall into
three basic categories: Projectiles (such as gun rounds), missiles
(including rockets), and bombs. Ordnance can be further defined by
their net explosive weight (NEW), which considers the type and quantity
of the explosive substance without the packaging, casings, bullets,
etc. NEW is the trinitrotoluene (TNT) equivalent of energetic material,
which is the standard measure of strength of bombs and other
explosives. For example, a 5-inch shell fired from a Navy gun is
analyzed at approximately 9.5 pounds (lb.) (4.3 kilograms [kg]) of NEW.
The Navy also uses non-explosive ordnance in place of explosive
ordnance in many training and testing events. Non-explosive ordnance
look and perform similarly to explosive ordnance, but lack the main
explosive charge.
Defense Countermeasures
Naval forces depend on effective defensive countermeasures to
protect themselves against missile and torpedo attack. Defensive
countermeasures are devices designed to confuse, distract, and confound
precision-guided munitions. Defensive countermeasures analyzed in this
LOA application include acoustic countermeasures, which are used by
surface ships and submarines to defend against torpedo attack. Acoustic
countermeasures are either released from ships and submarines, or towed
at a distance behind the ship.
Classification of Non-Impulsive and Impulsive Sources Analyzed
In order to better organize and facilitate the analysis of
approximately 300 individual sources of underwater acoustic sound or
explosive energy, a series of source classifications, or source bins,
were developed by the Navy. The use of source classification bins
provides the following benefits:
Provides the ability for new sensors or munitions to be
covered under existing regulatory authorizations, as long as those
sources fall within the parameters of a ``bin'';
Simplifies the source utilization data collection and
reporting requirements anticipated under the MMPA;
Ensures a conservative approach to all impact analysis, as
all sources in a single bin are modeled as the loudest source (e.g.,
lowest frequency, highest source level [the term ``source level''
refers to the loudness of a sound at its source], longest duty cycle,
or largest net explosive weight [NEW]) within that bin, which:
[cir] Allows analysis to be conducted more efficiently, without
compromising the results; and
[cir] Provides a framework to support the reallocation of source
usage (hours/explosives) between different source bins, as long as the
total number and severity of marine mammal takes remain within the
overall analyzed and authorized limits. This flexibility is required to
support evolving Navy training requirements, which are linked to real
world events.
There are two primary types of acoustic sources: Impulsive and non-
impulsive. A description of each source classification is provided in
Tables 1 and 2. Impulsive source class bins are based on the NEW of the
munitions or explosive devices or the source level for air and water
guns. Non-impulsive acoustic sources are grouped into source class bins
based on the frequency,\3\ source level,\4\ and, when warranted, the
application in which the source would be used. The following factors
further describe the considerations associated with the development of
non-impulsive source bins:
---------------------------------------------------------------------------
\3\ Bins are based on the typical center frequency of the
source. Although harmonics may be present, those harmonics would be
several decibels (dB) lower than the primary frequency.
\4\ Source decibel levels are expressed in terms of sound
pressure level (SPL) and are values given in dB referenced to 1
micropascal at 1 meter.
---------------------------------------------------------------------------
Frequency of the non-impulsive source.
[cir] Low-frequency sources operate below 1 kilohertz (kHz)
[cir] Mid-frequency sources operate at and above 1 kHz, up to and
including 10 kHz
[cir] High-frequency sources operate above 10 kHz, up to and including
100 kHz
[cir] Very high-frequency sources operate above 100 kHz but below 200
kHz
Source level of the non-impulsive source.
[cir] Greater than 160 decibels (dB), but less than 180 dB
[cir] Equal to 180 dB and up to 200 dB
[cir] Greater than 200 dB
Application in which the source would be used.
[cir] How a sensor is employed supports how the sensor's acoustic
emissions are analyzed.
[cir] Factors considered include pulse length (time source is on);
beam pattern (whether sound is emitted as a narrow, focused beam or, as
with most explosives, in all directions); and duty cycle (how often or
how many times a transmission occurs in a given time period during an
event).
As described in the GOA DSEIS/OEIS, non-impulsive acoustic sources
that have low source levels (not loud), narrow beam widths, downward
directed transmission, short pulse lengths, frequencies beyond known
hearing ranges of marine mammals, or some combination of these
characteristics, are not anticipated to result in takes of protected
species and therefore were not modeled. These sources generally meet
the following criteria and are qualitatively analyzed in the GOA DSEIS/
OEIS:
Acoustic sources with frequencies greater than 200 kHz (based
on known marine mammal hearing ranges)
Sources with source levels less than 160 dB
Table 1--Impulsive (Explosive) Training Source Classes Analyzed
------------------------------------------------------------------------
Representative Net explosive weight
Source class munitions (lbs)
------------------------------------------------------------------------
E5....................... 5-inch projectiles. >5-10
E6....................... AGM-114 Hellfire >10-20
missile.
E7....................... AGM-88 High-speed >20-60
Anti-Radiation
Missile.
E8....................... 250 lb. bomb....... >60-100
E9....................... 500 lb. bomb....... >100-250
[[Page 9954]]
E10...................... 1,000 lb. bomb/Air- >250-500
to-surface missile.
E11...................... MK-48 torpedo...... >500-650
E12...................... 2,000 lb. bomb..... >650-1,000
------------------------------------------------------------------------
Table 2--Non-Impulsive Training Source Classes Analyzed.
------------------------------------------------------------------------
Description of
Source class category Source class representative sources
------------------------------------------------------------------------
Mid-Frequency (MF): Tactical and MF1 Hull-mounted surface
non-tactical sources that ship sonar (e.g., AN/
produce mid-frequency (1-10 SQS-53C and AN/SQS-
kHz) signals. 60).
MF3 Hull-mounted submarine
sonar (e.g., AN/BQQ-
10).
MF4 Helicopter-deployed
dipping sonar (e.g.,
AN/AQS-22 and AN/AQS-
13).
MF5 Active acoustic
sonobuoys (e.g.,
DICASS).
MF6 Active underwater sound
signal devices (e.g.,
MK-84).
MF11 Hull-mounted surface
ship sonar with an
active duty cycle
greater than 80%.
High-Frequency (HF): Tactical HF1 Hull-mounted submarine
and non-tactical sources that HF6 sonar (e.g., AN/BQQ-
produce high[dash]frequency 10).
(greater than 10 kHz but less Active sources (equal
than 100 kHz) signals. to 180 dB and up to
200 dB).
Anti-Submarine Warfare (ASW): ASW2
Tactical sources such as active
sonobuoys and acoustic
countermeasures systems used
during the conduct of ASW
training activities.
ASW3 Mid-frequency
Multistatic Active
Coherent sonobuoy
(e.g., AN/SSQ-125).
Mid-frequency towed
active acoustic
countermeasure systems
(e.g., AN/SLQ-25).
ASW4 Mid-frequency
expendable active
acoustic device
countermeasures (e.g.,
MK-3).
Torpedoes (TORP): Source classes TORP2 Heavyweight torpedo
associated with the active (e.g., MK-48, electric
acoustic signals produced by vehicles).
torpedoes.
------------------------------------------------------------------------
Notes: dB = decibels, DICASS = Directional Command Activated Sonobuoy
System, kHz = kilohertz
Training
The training activities that the Navy proposes to conduct in the
Study Area are described in Table 3. The table is organized according
to primary mission areas and includes the activity name, associated
stressor(s), description of the activity, the primary platform used
(e.g., ship or aircraft type), duration of activity, type of non-
impulsive or impulsive sources used in the activity, and the number of
activities per year. More detailed activity descriptions can be found
in chapter 2 of the GOA DSEIS/OEIS. The Navy's Proposed Activities are
anticipated to meet training needs in the years 2016-2021.
Table 3--Training Activities Within the Study Area
----------------------------------------------------------------------------------------------------------------
Weapons/rounds/sound
Category Training activity Description source
----------------------------------------------------------------------------------------------------------------
Anti-Surface Warfare (ASUW)
Impulsive...................... Gunnery Exercise, Ship crews engage surface Small-, Medium-, and
Surface-to-Surface targets with ship's small- Large-caliber high
(Ship) (GUNEX-S-S , medium-, and large- explosive rounds.
[Ship]). caliber guns. Some of the
small- and medium-caliber
gunnery exercises analyzed
include those conducted by
the U.S. Coast Guard.
Impulsive...................... Sinking Exercise...... Fixed-wing aircrews, High explosive bombs,
surface ships and missiles, Large-
submarine firing precision- caliber rounds and
guided and non-precision torpedoes.
weapons against a surface
target.
Impulsive...................... Bombing Exercise (Air- Fixed-wing aircrews deliver High explosive bombs.
to-Surface) (BOMBEX bombs against surface
[A-S]). targets.
Anti-Submarine Warfare (ASW)
Non-impulsive.................. Tracking Exercise-- Submarine searches for, Mid- and high-
Submarine (TRACKEX-- detects, and tracks frequency submarine
Sub). submarine(s) and surface sonar.
ship(s).
[[Page 9955]]
Non-impulsive.................. Tracking Exercise-- Surface ship searches for, Mid-frequency surface
Surface (TRACKEX-- tracks, and detects ship sonar, acoustic
Surface). submarine(s). countermeasures, and
high-frequency active
sources.
Non-impulsive.................. Tracking Exercise-- Helicopter searches, Mid-frequency dipping
Helicopter (TRACKEX-- tracks, and detects sonar systems and
Helo). submarine(s). sonobuoys.
Non-impulsive.................. Tracking Exercise-- Maritime patrol aircraft Sonobuoys, such as
Maritime Patrol use sonobuoys to search DICASS sonobuoys.
Aircraft (TRACKEX-- for, detect, and track
MPA). submarine(s).
Non-impulsive.................. Tracking Exercise-- Maritime patrol aircraft mid-frequency MAC
Maritime Patrol crews search for, detect sonobuoys.
Aircraft (MAC and track submarines using
Sonobuoys). MAC sonobuoys.
----------------------------------------------------------------------------------------------------------------
Notes: DICASS = Directional Command Activated Sonobuoy System; MAC=Multistatic Active Coherent
Summary of Impulsive and Non-Impulsive Sources
Table 4 provides a quantitative annual summary of training
activities by sonar and other active acoustic source class analyzed in
the Navy's LOA request.
Table 4--Annual Hours of Sonar and Other Active Acoustic Sources Used During Training Within the Study Area
----------------------------------------------------------------------------------------------------------------
Source class category Source class Units Annual use
----------------------------------------------------------------------------------------------------------------
Mid-Frequency (MF) Active sources from 1 MF1....................... Hours..................... 541
to 10 kHz.
MF3....................... Hours..................... 48
MF4....................... Hours..................... 53
MF5....................... Items..................... 25
MF6....................... Items..................... 21
MF11...................... Hours..................... 78
High-Frequency (HF): Tactical and non- HF1....................... Hours..................... 24
tactical sources that produce signals HF6....................... Hours..................... 80
greater than 10 kHz but less than 100
kHz.
Anti-Submarine Warfare (ASW) Active ASW ASW2...................... Hours..................... 80
sources.
ASW3...................... Hours..................... 546
ASW4...................... Items..................... 4
Torpedoes (TORP) Source classes TORP2..................... Items..................... 5
associated with active acoustic signals
produced by torpedoes.
----------------------------------------------------------------------------------------------------------------
Table 5 provides a quantitative annual summary of training
explosive source classes analyzed in the Navy's LOA request.
Table 5--Annual Number of Training Explosive Source Detonations Used
During Training Within the Study Area
------------------------------------------------------------------------
Annual in-
water
Explosive class net explosive weight (pounds [lb.]) detonations
training
------------------------------------------------------------------------
E5 (> 5-10 lb.)......................................... 112
E6 (> 10-20 lb.)........................................ 2
E7 (> 20-60 lb.)........................................ 4
E8 (> 60-100 lb.)....................................... 6
E9 (> 100-250 lb.)...................................... 142
E10 (> 250-500 lb.)..................................... 32
E11 (> 500-650 lb.)..................................... 2
E12 (> 650-1,000 lb.)................................... 4
------------------------------------------------------------------------
Duration and Location
Training activities would be conducted in the Study Area during two
exercises of up to 21 days each per year (for a total of up to 42 days
per year) to support a major joint training exercise in Alaska and off
the Alaskan coast that involves the Departments of the Navy, the Army
and the Air Force, and the U.S. Coast Guard (Coast Guard). The Service
participants report to a unified or joint commander who coordinates the
activities planned to demonstrate and evaluate the ability of the
services to engage in a conflict and carry out plans in response to a
threat to national security. The exercises would occur between the
months of May and October of each year from 2016 to 2021.
The Study Area (see Figure 1-1 of the LOA application) is entirely
at sea and is composed of the established GOA TMAA and a warning area
in the Gulf of Alaska. The Navy uses ``at-sea'' to include its training
activities in the Study Area that occur (1) on the ocean surface, (2)
beneath the ocean surface, and (3) in the air above the ocean surface.
Navy training activities occurring on or over the land outside the GOA
TMAA are covered under previously prepared environmental documentation
prepared by the U.S. Air Force and the U.S. Army.
Gulf of Alaska Temporary Maritime Activities Area (GOA TMAA)
The GOA TMAA is a temporary area established in conjunction with
the Federal Aviation Administration (FAA) for up to two exercise
periods of up to 21 days each, for a total of 42 days per year, that is
a surface, undersea space, and airspace maneuver area within the Gulf
of Alaska for ships, submarines, and aircraft to conduct required
training activities. The GOA TMAA is a polygon roughly resembling a
rectangle oriented from northwest to southeast,
[[Page 9956]]
approximately 300 nautical miles (nm) in length by 150 nm in width,
located south of Prince William Sound and east of Kodiak Island.
Airspace of the GOA TMAA
The airspace of the GOA TMAA overlies the surface and subsurface
training area and is called an Altitude Reservation (ALTRV). This ALTRV
is a temporary airspace designation, typically requested by the Alaskan
Command (ALCOM) and coordinated through the FAA for the duration of the
exercise. This overwater airspace supports the majority of aircraft
training activities conducted by Navy and Joint aircraft throughout the
joint training exercise. The ALTRV over the GOA TMAA typically extends
from the ocean surface to 60,000 feet (ft.) (18,288 meters [m]) above
mean sea level and encompasses 42,146 square nautical miles (nm\2\) of
airspace. For safety considerations, ALTRV information is sent via
Notice to Airmen (NOTAM)/International NOTAM so that all pilots are
aware of the area and that Air Traffic Control will keep known
Instrument Flight Rules aircraft clear of the area.
Additionally, the GOA TMAA overlies a majority of Warning Area W-
612 (W-612) located over Blying Sound, towards the northwestern
quadrant of the GOA TMAA. When not included as part of the GOA TMAA, W-
612 provides 2,256 nm\2\ of special use airspace for the Air Force and
Coast Guard to fulfill some of their training requirements. Air Force,
Army, National Guard, and Coast Guard activities conducted as part of
at-sea joint training within the GOA TMAA are included in the DSEIS/
OEIS analysis. No Navy training activities analyzed in this proposed
rule occur in the area of W-612 that is outside of the GOA TMAA (see
Figure 1-1 of the LOA application).
Sea and Undersea Space of the GOA TMAA
The GOA TMAA surface and subsurface areas are also depicted in
Figure 1-1 of the LOA application. Total surface area of the GOA TMAA
is 42,146 nm\2\. Due to weather conditions, annual joint training
activities are typically conducted during the summer months (April-
October). The GOA TMAA undersea area lies beneath the surface area as
depicted in Figure 1-1 of the LOA application. The undersea area
extends to the seafloor.
The complex bathymetric and oceanographic conditions, including a
continental shelf, submarine canyons, numerous seamounts, and fresh
water infusions from multiple sources, create a challenging environment
in which to search for and detect submarines in ASW training
activities. In the summer, the GOA TMAA provides a safe cold-water
training environment that resembles other areas where Navy may need to
operate in a real-world scenario.
The GOA TMAA meets large-scale joint exercise training objectives
to support naval and joint operational readiness by providing a
``geographically realistic'' training area for U.S. Pacific Command,
Joint Task Force Commander scenario-based training, and supports the
mission requirement of Alaskan Command (ALCOM) to conduct joint
training for Alaska-based forces. The strategic vision of the
Commander, U.S. Pacific Fleet is that the training area support naval
operational readiness by providing a realistic, live-training
environment for forces assigned to the Pacific Fleet and other users
with the capability and capacity to support current, emerging, and
future training requirements.
Description of Marine Mammals in the Area of the Specified Activities
Marine mammal species known to occur in the Study Area and their
currently recognized stocks are presented in Table 6 consistent with
the NMFS' U.S. Pacific Marine Mammal Stock Assessment Report (Carretta
et al., 2015) and the Alaska Marine Mammal Stock Assessment Report
(Muto and Angliss, 2015). Twenty-two marine mammal species have
confirmed or possible occurrence within or adjacent to the Study Area,
including seven species of baleen whales (mysticetes), eight species of
toothed whales (odontocetes), six species of seals (pinnipeds), and the
sea otter (mustelid). Nine of these species are listed under the ESA:
Blue whale, fin whale, humpback whale, sei whale, sperm whale, gray
whale (Western North Pacific stock), North Pacific right whale, Steller
sea lion (Western U.S. stock), and sea otter. All these species are
managed by NMFS or the U.S. Fish and Wildlife Service (USFWS) in the
U.S. Exclusive Economic Zone (EEZ).
The species carried forward for analysis are those likely to be
found in the Study Area based on the most recent data available, and do
not include stocks or species that may have once inhabited or transited
the area but have not been sighted in recent years (e.g., species which
were extirpated because of factors such as nineteenth and twentieth
century commercial exploitation). Several species that may be present
in the Gulf of Alaska have an extremely low probability of presence in
the Study Area. These species are considered extralimital, meaning
there may be a small number of sighting or stranding records within the
Study Area, but the area of concern is outside the species' range of
normal occurrence. These species include beluga whale (Delphinapterus
leucas), false killer whale (Pseudorca crassidens), short-finned pilot
whale (Globicephala macrorhynchus), northern right whale dolphin
(Lissodelphis borealis), and Risso's dolphin (Grampus griseus), and
have been excluded from subsequent analysis.
Table 6--Marine Mammals With Possible or Confirmed Presence Within the Study Area
--------------------------------------------------------------------------------------------------------------------------------------------------------
Stock abundance \3\ Occurrence in region
Common name Scientific name \1\ Stock \2\ (CV) \4\ ESA/MMPA Status
--------------------------------------------------------------------------------------------------------------------------------------------------------
Order Cetacea
Suborder Mysticeti (baleen whales)
Family Balaenidae (right whales)
--------------------------------------------------------------------------------------------------------------------------------------------------------
North Pacific right whale.......... Eubalaena japonica.... Eastern North Pacific. 31 (0.23)............ Rare................. Endangered/Depleted.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Balaenopteridae (rorquals)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Humpback whale..................... Megaptera novaeangliae Central North Pacific. 10,252 (0.042)....... Likely............... Endangered/ Depleted.
Western North Pacific. 893 (0.079).......... Likely............... Endangered/ Depleted.
[[Page 9957]]
Blue whale......................... Balaenoptera musculus. Eastern North Pacific. 1,647 (0.07)......... Seasonal; highest Endangered/ Depleted.
likelihood July to
December.
Central North Pacific. 81 (1.14)............ Seasonal; highest Endangered/ Depleted.
likelihood July to
December.
Fin whale.......................... Balaenoptera physalus. Northeast Pacific..... 1,368 (minimum Likely............... Endangered/ Depleted.
estimate) (n/a).
Sei whale.......................... Balaenoptera borealis. Eastern North Pacific. 126 (0.53)........... Rare................. Endangered/ Depleted.
Minke whale........................ Balaenoptera Alaska................ Not available........ Likely.
acutorostrata.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Eschrichtiidae (gray whale)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Gray whale......................... Eschrichtius robustus. Eastern North Pacific. 20,990 (0.05)........ Likely: Highest
numbers during
seasonal migrations.
Western North Pacific. 140 (0.043).......... Rare: Individuals Endangered/ Depleted.
migrate through GOA.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Suborder Odontoceti (toothed whales)
Family Physeteridae (sperm whale)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sperm whale........................ Physeter macrocephalus North Pacific......... Not available........ Likely; More likely Endangered/ Depleted.
in waters > 1,000 m
depth, most often >
2,000 m.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Delphinidae (dolphins)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Killer whale....................... Orcinus orca.......... Alaska Resident....... 2,347 (n/a).......... Likely.
Eastern North Pacific 211: includes known Infrequent: few
Offshore. offshore killer sightings.
whales along the
U.S. west coast,
Canada, and Alaska
(n/a).
AT1 Transient......... 7.................... Rare; more likely
inside Prince
William Sound and
Kenai Fjords.
GOA, Aleutian Island, 587.................. Likely.
and Bering Sea
Transient.
Pacific white[dash]sided dolphin... Lagenorhynchus North Pacific......... 26,880; specific to Likely.
obliquidens. the GOA, not the
management stock (n/
a).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Phocoenidae (porpoises)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Harbor porpoise.................... Phocoena phocoena..... GOA................... 31,046 (0.21)........ Likely in nearshore
locations.
Southeast Alaska...... 11,146 (0.24)........ Likely in nearshore
locations.
Dall's porpoise.................... Phocoenoides dalli.... Alaska................ 83,400 (0.097); based Likely.
on survey data from
1987-1991.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Ziphiidae (beaked whales)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cuvier's beaked whale.............. Ziphius cavirostris... Alaska................ Not available........ Likely.
Baird's beaked whale............... Berardius bairdii..... Alaska................ Not available........ Likely.
Stejneger's beaked whale........... Mesoplodon stejnegeri. Alaska................ Not available........ Likely.
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 9958]]
Order Carnivora
Suborder Pinnipedia \5\
Family Otariidae (fur seals and sea lions)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Steller sea lion................... Eumetopias jubatus.... Eastern U.S........... 59,968 (minimum Likely.
estimate) (n/a).
Western U.S........... 49,497 (minimum Likely............... Endangered/ Depleted.
estimate) (n/a).
California sea lion................ Zalophus californianus U.S................... 296,750 (n/a)........ Rare.
Northern fur seal.................. Callorhinus ursinus... Eastern Pacific....... 648,534 (n/a)........ Likely............... Depleted.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Phocidae (true seals)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Northern elephant seal............. Mirounga California Breeding... 179,000 (n/a)........ Likely.
angustirostris.
Harbor seal........................ Phoca vitulina........ Aleutian Islands...... 6,431 (n/a).......... Extralimital
Pribilof Islands...... 232 (n/a)............ Extralimital.
Bristol Bay........... 32,350 (n/a)......... Extralimital.
N. Kodiak............. 8,321 (n/a).......... Rare (inshore
waters).
S. Kodiak............. 19,199 (n/a)......... Rare (inshore
waters).
Prince William Sound.. 29,889 (n/a)......... Rare (inshore
waters).
Cook Inlet/Shelikof... 27,386 (n/a)......... Extralimital.
Glacier Bay/Icy Strait 7,210 (n/a).......... Rare (inshore
waters).
Lynn Canal/ Stephens.. 9,478 (n/a).......... Extralimital.
Sitka/Chatham......... 14,855 (n/a)......... Rare (inshore
waters).
Dixon/Cape Decision... 18,105 (n/a)......... Rare (inshore
waters).
Clarence Strait....... 31,634 (n/a)......... Extralimital.
Ribbon seal........................ Histriophoca fasciata. Alaska................ 184,000.............. Rare.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Mustelidae (otters) \6\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Northern sea otter................. Enhydra lutris kenyoni Southeast Alaska...... 10,563............... Rare.
Southcentral Alaska... 15,090............... Rare.
Southwest Alaska...... 47,676............... Rare................. Threatened.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ Taxonomy follows Perrin et al. (2009).
\2\ Stock names and abundance estimates from Muto and Angliss (2015) and Carretta et al. (2015) except where noted.
\3\ The stated coefficient of variation (CV) from the NMFS Stock Assessement Reports is an indicator of uncertainty in the abundance estimate and
describes the amount of variation with respect to the population mean. It is expressed as a fraction or sometimes a percentage and can range upward
from zero, indicating no uncertainty, to high values. For example, a CV of 0.85 would indicate high uncertainty in the population estimate. When the
CV exceeds 1.0, the estimate is very uncertain. The uncertainty associated with movements of animals into or out of an area (due to factors such as
availability of prey or changing oceanographic conditions) is much larger than is indicated by the CVs that are given.
\4\ EXTRALIMITAL: There may be a small number of sighting or stranding records, but the area is outside the species range of normal occurrence. RARE:
The distribution of the species is near enough to the area that the species could occur there, or there are a few confirmed sightings. INFREQUENT:
Confirmed, but irregular sightings or acoustic detections. LIKELY: Confirmed and regular sightings or acoustic detections of the species in the area
year-round. SEASONAL: Confirmed and regular sightings or acoustic detections of the species in the area on a seasonal basis.
\5\ There are no data regarding the CV for some of the pinniped species given that abundance is determined by different methods than those used for
cetaceans.
\6\ There are no data regarding the CV for sea otter given that abundance is determined by different methods than those used for cetaceans.
Notes: CV = coefficient of variation, ESA = Endangered Species Act, GOA = Gulf of Alaska, m = meter(s), MMPA = Marine Mammal Protection Act, n/a = not
available, U.S. = United States.
Information on the status, distribution, abundance, and
vocalizations of marine mammal species in the Study Area may be viewed
in Chapter 4 of the LOA application (https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm). Additional information on the general
biology and ecology of marine mammals are included in the GOA DSEIS/
OEIS. In addition, NMFS annually publishes Stock Assessment Reports
(SARs) for all marine mammals in U.S. EEZ waters, including stocks that
occur within the Study Area (U.S. Pacific Marine Mammal Stock
Assessments, Carretta et al., 2015; Alaska Marine Mammal Stock
Assessments, Muto and Angliss, 2015).
Marine Mammal Hearing and Vocalizations
Cetaceans have an auditory anatomy that follows the basic mammalian
pattern, with some changes to adapt to the demands of hearing
underwater. The typical mammalian ear is divided into an outer ear,
middle ear, and inner ear.
[[Page 9959]]
The outer ear is separated from the inner ear by a tympanic membrane,
or eardrum. In terrestrial mammals, the outer ear, eardrum, and middle
ear transmit airborne sound to the inner ear, where the sound waves are
propagated through the cochlear fluid. Since the impedance of water is
close to that of the tissues of a cetacean, the outer ear is not
required to transduce sound energy as it does when sound waves travel
from air to fluid (inner ear). Sound waves traveling through the inner
ear cause the basilar membrane to vibrate. Specialized cells, called
hair cells, respond to the vibration and produce nerve pulses that are
transmitted to the central nervous system. Acoustic energy causes the
basilar membrane in the cochlea to vibrate. Sensory cells at different
positions along the basilar membrane are excited by different
frequencies of sound (Pickles, 1998).
Marine mammal vocalizations often extend both above and below the
range of human hearing; vocalizations with frequencies lower than 20 Hz
are labeled as infrasonic and those higher than 20 kHz as ultrasonic
(National Research Council (NRC), 2003; Figure 4-1). Measured data on
the hearing abilities of cetaceans are sparse, particularly for the
larger cetaceans such as the baleen whales. The auditory thresholds of
some of the smaller odontocetes have been determined in captivity. It
is generally believed that cetaceans should at least be sensitive to
the frequencies of their own vocalizations. Comparisons of the anatomy
of cetacean inner ears and models of the structural properties and the
response to vibrations of the ear's components in different species
provide an indication of likely sensitivity to various sound
frequencies. The ears of small toothed whales are optimized for
receiving high-frequency sound, while baleen whale inner ears are best
in low to infrasonic frequencies (Ketten, 1992; 1997; 1998).
Baleen whale vocalizations are composed primarily of frequencies
below 1 kHz, and some contain fundamental frequencies as low as 16 Hz
(Watkins et al., 1987; Richardson et al., 1995; Rivers, 1997; Moore et
al., 1998; Stafford et al., 1999; Wartzok and Ketten, 1999) but can be
as high as 24 kHz (humpback whale; Au et al., 2006). Clark and Ellison
(2004) suggested that baleen whales use low-frequency sounds not only
for long-range communication, but also as a simple form of echo
ranging, using echoes to navigate and orient relative to physical
features of the ocean. Information on auditory function in baleen
whales is extremely lacking. Sensitivity to low-frequency sound by
baleen whales has been inferred from observed vocalization frequencies,
observed reactions to playback of sounds, and anatomical analyses of
the auditory system. Although there is apparently much variation, the
source levels of most baleen whale vocalizations lie in the range of
150-190 dB re 1 microPascal ([micro]Pa) at 1 m. Low-frequency
vocalizations made by baleen whales and their corresponding auditory
anatomy suggest that they have good low-frequency hearing (Ketten,
2000), although specific data on sensitivity, frequency or intensity
discrimination, or localization abilities are lacking. Marine mammals,
like all mammals, have typical U-shaped audiograms that begin with
relatively low sensitivity (high threshold) at some specified low
frequency with increased sensitivity (low threshold) to a species
specific optimum followed by a generally steep rise at higher
frequencies (high threshold) (Fay, 1988).
The toothed whales produce a wide variety of sounds, which include
species-specific broadband ``clicks'' with peak energy between 10 and
200 kHz, individually variable ``burst pulse'' click trains, and
constant frequency or frequency-modulated (FM) whistles ranging from 4
to 16 kHz (Wartzok and Ketten, 1999). The general consensus is that the
tonal vocalizations (whistles) produced by toothed whales play an
important role in maintaining contact between dispersed individuals,
while broadband clicks are used during echolocation (Wartzok and
Ketten, 1999). Burst pulses have also been strongly implicated in
communication, with some scientists suggesting that they play an
important role in agonistic encounters (McCowan and Reiss, 1995), while
others have proposed that they represent ``emotive'' signals in a
broader sense, possibly representing graded communication signals
(Herzing, 1996). Sperm whales, however, are known to produce only
clicks, which are used for both communication and echolocation
(Whitehead, 2003). Most of the energy of toothed whale social
vocalizations is concentrated near 10 kHz, with source levels for
whistles as high as 100 to 180 dB re 1 [micro]Pa at 1 m (Richardson et
al., 1995). No odontocete has been shown audiometrically to have acute
hearing (<80 dB re 1 [micro]Pa) below 500 Hz (DoN, 2001). Sperm whales
produce clicks, which may be used to echolocate (Mullins et al., 1988),
with a frequency range from less than 100 Hz to 30 kHz and source
levels up to 230 dB re 1 [micro]Pa 1 m or greater (Mohl et al., 2000).
Brief Background on Sound
An understanding of the basic properties of underwater sound is
necessary to comprehend many of the concepts and analyses presented in
this proposed rule. A summary is included below.
Sound is a wave of pressure variations propagating through a medium
(e.g., water). Pressure variations are created by compressing and
relaxing the medium. Sound measurements can be expressed in two forms:
Intensity and pressure. Acoustic intensity is the average rate of
energy transmitted through a unit area in a specified direction and is
expressed in watts per square meter (W/m\2\). Acoustic intensity is
rarely measured directly, but rather from ratios of pressures; the
standard reference pressure for underwater sound is 1 [micro]Pa; for
airborne sound, the standard reference pressure is 20 [micro]Pa
(Richardson et al., 1995).
Acousticians have adopted a logarithmic scale for sound
intensities, which is denoted in decibels (dB). Decibel measurements
represent the ratio between a measured pressure value and a reference
pressure value (in this case 1 [micro]Pa or, for airborne sound, 20
[micro]Pa). The logarithmic nature of the scale means that each 10-dB
increase is a ten-fold increase in acoustic power (and a 20-dB increase
is then a 100-fold increase in power; and a 30-dB increase is a 1,000-
fold increase in power). A ten-fold increase in acoustic power does not
mean that the sound is perceived as being ten times louder, however.
Humans perceive a 10-dB increase in sound level as a doubling of
loudness, and a 10-dB decrease in sound level as a halving of loudness.
The term ``sound pressure level'' implies a decibel measure and a
reference pressure that is used as the denominator of the ratio.
Throughout this proposed rule, NMFS uses 1 [micro]Pa (denoted re:
1[micro]Pa) as a standard reference pressure unless noted otherwise.
It is important to note that decibel values underwater and decibel
values in air are not the same (different reference pressures and
densities/sound speeds between media) and should not be directly
compared. Because of the different densities of air and water and the
different decibel standards (i.e., reference pressures) in air and
water, a sound with the same level in air and in water would be
approximately 62 dB lower in air. Thus, a sound that measures 160 dB
(re 1 [micro]Pa) underwater would have the same approximate effective
level as a sound that is 98 dB (re 20 [micro]Pa) in air.
[[Page 9960]]
Sound frequency is measured in cycles per second, or Hertz
(abbreviated Hz), and is analogous to musical pitch; high-pitched
sounds contain high frequencies and low-pitched sounds contain low
frequencies. Natural sounds in the ocean span a huge range of
frequencies: From earthquake noise at 5 Hz to harbor porpoise clicks at
150,000 Hz (150 kHz). These sounds are so low or so high in pitch that
humans cannot even hear them; acousticians call these infrasonic
(typically below 20 Hz) and ultrasonic (typically above 20,000 Hz)
sounds, respectively. A single sound may be made up of many different
frequencies together. Sounds made up of only a small range of
frequencies are called ``narrowband'', and sounds with a broad range of
frequencies are called ``broadband''; explosives are an example of a
broadband sound source and active tactical sonars are an example of a
narrowband sound source.
When considering the influence of various kinds of sound on the
marine environment, it is necessary to understand that different kinds
of marine life are sensitive to different frequencies of sound. Current
data indicate that not all marine mammal species have equal hearing
capabilities (Richardson et al., 1995; Southall et al., 1997; Wartzok
and Ketten, 1999; Au and Hastings, 2008).
Southall et al. (2007) designated ``functional hearing groups'' for
marine mammals based on available behavioral data; audiograms derived
from auditory evoked potentials; anatomical modeling; and other data.
Southall et al. (2007) also estimated the lower and upper frequencies
of functional hearing for each group. However, animals are less
sensitive to sounds at the outer edges of their functional hearing
range and are more sensitive to a range of frequencies within the
middle of their functional hearing range. Note that direct measurements
of hearing sensitivity do not exist for all species of marine mammals,
including low-frequency cetaceans. The functional hearing groups and
the associated frequencies developed by Southall et al. (2007) were
revised by Finneran and Jenkins (2012) and have been further modified
by NOAA. Table 7 provides a summary of sound production and general
hearing capabilities for marine mammal species (note that values in
this table are not meant to reflect absolute possible maximum ranges,
rather they represent the best known ranges of each functional hearing
group). For purposes of the analysis in this proposed rule, marine
mammals are arranged into the following functional hearing groups based
on their generalized hearing sensitivities: High-frequency cetaceans,
mid-frequency cetaceans, low-frequency cetaceans (mysticetes), phocids
(true seals), otariids (sea lion and fur seals), and mustelids (sea
otters). A detailed discussion of the functional hearing groups can be
found in Southall et al. (2007) and Finneran and Jenkins (2012).
Table 7--Marine Mammal Functional Hearing Groups
------------------------------------------------------------------------
Functional hearing group Functional hearing range *
------------------------------------------------------------------------
Low-frequency (LF) cetaceans (baleen 7 Hz to 25 kHz.
whales).
Mid-frequency (MF) cetaceans 150 Hz to 160 kHz.
(dolphins, toothed whales, beaked
whales, bottlenose whales).
High-frequency (HF) cetaceans (true 200 Hz to 180 kHz.
porpoises, Kogia, river dolphins,
cephalorhynchid, Lagenorhynchus
cruciger & L. australis).
Phocid pinnipeds (underwater) (true 75 Hz to 100 kHz.
seals).
Otariid pinnipeds (underwater) (sea 100 Hz to 48 kHz.
lions and fur seals).
------------------------------------------------------------------------
Adapted and derived from Southall et al. (2007)
* Represents frequency band of hearing for entire group as a composite
(i.e., all species within the group), where individual species'
hearing ranges are typically not as broad. Functional hearing is
defined as the range of frequencies a group hears without
incorporating non-acoustic mechanisms (Wartzok and Ketten, 1999). This
is ~60 to ~70 dB above best hearing sensitivity (Southall et al.,
2007) for all functional hearing groups except LF cetaceans, where no
direct measurements on hearing are available. For LF cetaceans, the
lower range is based on recommendations from Southall et al., 2007 and
the upper range is based on information on inner ear anatomy and
vocalizations.
When sound travels (propagates) from its source, its loudness
decreases as the distance traveled by the sound increases. Thus, the
loudness of a sound at its source is higher than the loudness of that
same sound a kilometer away. Acousticians often refer to the loudness
of a sound at its source (typically referenced to one meter from the
source) as the source level and the loudness of sound elsewhere as the
received level (i.e., typically the receiver). For example, a humpback
whale 3 km from a device that has a source level of 230 dB may only be
exposed to sound that is 160 dB loud, depending on how the sound
travels through water (e.g., spherical spreading [3 dB reduction with
doubling of distance] was used in this example). As a result, it is
important to understand the difference between source levels and
received levels when discussing the loudness of sound in the ocean or
its impacts on the marine environment.
As sound travels from a source, its propagation in water is
influenced by various physical characteristics, including water
temperature, depth, salinity, and surface and bottom properties that
cause refraction, reflection, absorption, and scattering of sound
waves. Oceans are not homogeneous and the contribution of each of these
individual factors is extremely complex and interrelated. The physical
characteristics that determine the sound's speed through the water will
change with depth, season, geographic location, and with time of day
(as a result, in actual active sonar operations, crews will measure
oceanic conditions, such as sea water temperature and depth, to
calibrate models that determine the path the sonar signal will take as
it travels through the ocean and how strong the sound signal will be at
a given range along a particular transmission path). As sound travels
through the ocean, the intensity associated with the wavefront
diminishes, or attenuates. This decrease in intensity is referred to as
propagation loss, also commonly called transmission loss.
Metrics Used in This Proposed Rule
This section includes a brief explanation of the two sound
measurements (sound pressure level (SPL) and sound exposure level
(SEL)) frequently used to describe sound levels in the discussions of
acoustic effects in this proposed rule.
Sound pressure level (SPL)--Sound pressure is the sound force per
unit area, and is usually measured in micropascals ([micro]Pa), where 1
Pa is the pressure resulting from a force of one newton exerted over an
area of one square meter. SPL is expressed as the
[[Page 9961]]
ratio of a measured sound pressure and a reference level.
SPL (in dB) = 20 log (pressure/reference pressure)
The commonly used reference pressure level in underwater acoustics
is 1 [micro]Pa, and the units for SPLs are dB re: 1 [micro]Pa. SPL is
an instantaneous pressure measurement and can be expressed as the peak,
the peak-peak, or the root mean square (rms). Root mean square
pressure, which is the square root of the arithmetic average of the
squared instantaneous pressure values, is typically used in discussions
of the effects of sounds on vertebrates and all references to SPL in
this proposed rule refer to the root mean square. SPL does not take the
duration of exposure into account. SPL is the applicable metric used in
the risk continuum, which is used to estimate behavioral harassment
takes (see Level B Harassment Risk Function (Behavioral Harassment)
Section).
Sound exposure level (SEL)--SEL is an energy metric that integrates
the squared instantaneous sound pressure over a stated time interval.
The units for SEL are dB re: 1 [micro]Pa\2\-s. Below is a simplified
formula for SEL.
SEL = SPL + 10log (duration in seconds)
As applied to active sonar, the SEL includes both the SPL of a
sonar ping and the total duration. Longer duration pings and/or pings
with higher SPLs will have a higher SEL. If an animal is exposed to
multiple pings, the SEL in each individual ping is summed to calculate
the cumulative SEL. The cumulative SEL depends on the SPL, duration,
and number of pings received. The thresholds that NMFS uses to indicate
at what received level the onset of temporary threshold shift (TTS) and
permanent threshold shift (PTS) in hearing are likely to occur are
expressed as cumulative SEL.
Potential Effects of Specified Activities on Marine Mammals
The Navy has requested authorization for the take of marine mammals
that may occur incidental to training activities in the Study Area. The
Navy has analyzed potential impacts to marine mammals from impulsive
and non-impulsive sound sources.
Other potential impacts to marine mammals from training activities
in the Study Area were analyzed in the GOA DSEIS/OEIS, in consultation
with NMFS as a cooperating agency, and determined to be unlikely to
result in marine mammal harassment. Therefore, the Navy has not
requested authorization for take of marine mammals that might occur
incidental to other components of their proposed activities. In this
proposed rule, NMFS analyzes the potential effects on marine mammals
from exposure to non-impulsive sound sources (sonar and other active
acoustic sources) and impulsive sound sources (underwater detonations).
For the purpose of MMPA authorizations, NMFS' effects assessments
serve four primary purposes: (1) To prescribe the permissible methods
of taking (i.e., Level B harassment (behavioral harassment), Level A
harassment (injury), or mortality, including an identification of the
number and types of take that could occur by harassment or mortality)
and to prescribe other means of effecting the least practicable adverse
impact on such species or stock and its habitat (i.e., mitigation); (2)
to determine whether the specified activity would have a negligible
impact on the affected species or stocks of marine mammals (based on
the likelihood that the activity would adversely affect the species or
stock through effects on annual rates of recruitment or survival); (3)
to determine whether the specified activity would have an unmitigable
adverse impact on the availability of the species or stock(s) for
subsistence uses; and (4) to prescribe requirements pertaining to
monitoring and reporting.
This section focuses qualitatively on the different ways that non-
impulsive and impulsive sources may affect marine mammals (some of
which NMFS would not classify as harassment). Then the Estimated Take
of Marine Mammals section discusses how the potential effects of non-
impulsive and impulsive sources on marine mammals will be related to
the MMPA definitions of Level A and Level B Harassment, and attempts to
quantify those effects.
Non-impulsive Sources
Direct Physiological Effects
Based on the literature, there are two basic ways that non-
impulsive sources might directly result in physical trauma or damage:
Noise-induced loss of hearing sensitivity (more commonly-called
``threshold shift'') and acoustically mediated bubble growth.
Separately, an animal's behavioral reaction to an acoustic exposure
might lead to physiological effects that might ultimately lead to
injury or death, which is discussed later in the Stranding section.
Threshold Shift (noise-induced loss of hearing)--When animals
exhibit reduced hearing sensitivity (i.e., sounds must be louder for an
animal to detect them) following exposure to an intense sound or sound
for long duration, it is referred to as a noise-induced threshold shift
(TS). An animal can experience temporary threshold shift (TTS) or
permanent threshold shift (PTS). TTS can last from minutes or hours to
days (i.e., there is complete recovery), can occur in specific
frequency ranges (i.e., an animal might only have a temporary loss of
hearing sensitivity between the frequencies of 1 and 10 kHz), and can
be of varying amounts (for example, an animal's hearing sensitivity
might be reduced initially by only 6 dB or reduced by 30 dB). PTS is
permanent, but some recovery is possible. PTS can also occur in a
specific frequency range and amount, as mentioned above for TTS.
The following physiological mechanisms are thought to play a role
in inducing auditory TS: Effects to sensory hair cells in the inner ear
that reduce their sensitivity, modification of the chemical environment
within the sensory cells, residual muscular activity in the middle ear,
displacement of certain inner ear membranes, increased blood flow, and
post-stimulatory reduction in both efferent and sensory neural output
(Southall et al., 2007). The amplitude, duration, frequency, temporal
pattern, and energy distribution of sound exposure all can affect the
amount of associated TS and the frequency range in which it occurs. As
amplitude and duration of sound exposure increase, so, generally, does
the amount of TS, along with the recovery time. For intermittent
sounds, less TS could occur than compared to a continuous exposure with
the same energy (some recovery could occur between intermittent
exposures depending on the duty cycle between sounds) (Kryter et al.,
1966; Ward, 1997). For example, one short but loud (higher SPL) sound
exposure may induce the same impairment as one longer but softer sound,
which in turn may cause more impairment than a series of several
intermittent softer sounds with the same total energy (Ward, 1997).
Additionally, though TTS is temporary, prolonged exposure to sounds
strong enough to elicit TTS, or shorter-term exposure to sound levels
well above the TTS threshold, can cause PTS, at least in terrestrial
mammals (Kryter, 1985). Although in the case of mid- and high-frequency
active sonar (MFAS/HFAS), animals are not expected to be exposed to
levels high enough or durations long enough to result in PTS.
PTS is considered auditory injury (Southall et al., 2007).
Irreparable damage to the inner or outer cochlear hair cells may cause
PTS; however,
[[Page 9962]]
other mechanisms are also involved, such as exceeding the elastic
limits of certain tissues and membranes in the middle and inner ears
and resultant changes in the chemical composition of the inner ear
fluids (Southall et al., 2007).
Although the published body of scientific literature contains
numerous theoretical studies and discussion papers on hearing
impairments that can occur with exposure to a loud sound, only a few
studies provide empirical information on the levels at which noise-
induced loss in hearing sensitivity occurs in nonhuman animals. For
marine mammals, published data are limited to the captive bottlenose
dolphin, beluga, harbor porpoise, and Yangtze finless porpoise
(Finneran et al., 2000, 2002b, 2003, 2005a, 2007, 2010a, 2010b;
Finneran and Schlundt, 2010; Lucke et al., 2009; Mooney et al., 2009a,
2009b; Popov et al., 2011a, 2011b; Kastelein et al., 2012a; Schlundt et
al., 2000; Nachtigall et al., 2003, 2004). For pinnipeds in water, data
are limited to measurements of TTS in harbor seals, an elephant seal,
and California sea lions (Kastak et al., 1999, 2005; Kastelein et al.,
2012b).
Marine mammal hearing plays a critical role in communication with
conspecifics, and interpretation of environmental cues for purposes
such as predator avoidance and prey capture. Depending on the degree
(elevation of threshold in dB), duration (i.e., recovery time), and
frequency range of TTS, and the context in which it is experienced, TTS
can have effects on marine mammals ranging from discountable to serious
(similar to those discussed in auditory masking, below). For example, a
marine mammal may be able to readily compensate for a brief, relatively
small amount of TTS in a non-critical frequency range that occurs
during a time where ambient noise is lower and there are not as many
competing sounds present. Alternatively, a larger amount and longer
duration of TTS sustained during time when communication is critical
for successful mother/calf interactions could have more serious
impacts. Also, depending on the degree and frequency range, the effects
of PTS on an animal could range in severity, although it is considered
generally more serious because it is a permanent condition. Of note,
reduced hearing sensitivity as a simple function of aging has been
observed in marine mammals, as well as humans and other taxa (Southall
et al., 2007), so one can infer that strategies exist for coping with
this condition to some degree, though likely not without cost.
Acoustically Mediated Bubble Growth--One theoretical cause of
injury to marine mammals is rectified diffusion (Crum and Mao, 1996),
the process of increasing the size of a bubble by exposing it to a
sound field. This process could be facilitated if the environment in
which the ensonified bubbles exist is supersaturated with gas.
Repetitive diving by marine mammals can cause the blood and some
tissues to accumulate gas to a greater degree than is supported by the
surrounding environmental pressure (Ridgway and Howard, 1979). The
deeper and longer dives of some marine mammals (for example, beaked
whales) are theoretically predicted to induce greater supersaturation
(Houser et al., 2001b). If rectified diffusion were possible in marine
mammals exposed to high-level sound, conditions of tissue
supersaturation could theoretically speed the rate and increase the
size of bubble growth. Subsequent effects due to tissue trauma and
emboli would presumably mirror those observed in humans suffering from
decompression sickness.
It is unlikely that the short duration of sonar pings would be long
enough to drive bubble growth to any substantial size, if such a
phenomenon occurs. However, an alternative but related hypothesis has
also been suggested: Stable bubbles could be destabilized by high-level
sound exposures such that bubble growth then occurs through static
diffusion of gas out of the tissues. In such a scenario the marine
mammal would need to be in a gas-supersaturated state for a long enough
period of time for bubbles to become of a problematic size. Recent
research with ex vivo supersaturated bovine tissues suggested that, for
a 37 kHz signal, a sound exposure of approximately 215 dB referenced to
(re) 1 [mu]Pa would be required before microbubbles became destabilized
and grew (Crum et al., 2005). Assuming spherical spreading loss and a
nominal sonar source level of 235 dB re 1 [mu]Pa at 1 m, a whale would
need to be within 10 m (33 ft.) of the sonar dome to be exposed to such
sound levels. Furthermore, tissues in the study were supersaturated by
exposing them to pressures of 400-700 kilopascals for periods of hours
and then releasing them to ambient pressures. Assuming the
equilibration of gases with the tissues occurred when the tissues were
exposed to the high pressures, levels of supersaturation in the tissues
could have been as high as 400-700 percent. These levels of tissue
supersaturation are substantially higher than model predictions for
marine mammals (Houser et al., 2001; Saunders et al., 2008). It is
improbable that this mechanism is responsible for stranding events or
traumas associated with beaked whale strandings. Both the degree of
supersaturation and exposure levels observed to cause microbubble
destabilization are unlikely to occur, either alone or in concert.
Yet another hypothesis (decompression sickness) has speculated that
rapid ascent to the surface following exposure to a startling sound
might produce tissue gas saturation sufficient for the evolution of
nitrogen bubbles (Jepson et al., 2003; Fernandez et al., 2005;
Fern[aacute]ndez et al., 2012). In this scenario, the rate of ascent
would need to be sufficiently rapid to compromise behavioral or
physiological protections against nitrogen bubble formation.
Alternatively, Tyack et al. (2006) studied the deep diving behavior of
beaked whales and concluded that: ``Using current models of breath-hold
diving, we infer that their natural diving behavior is inconsistent
with known problems of acute nitrogen supersaturation and embolism.''
Collectively, these hypotheses can be referred to as ``hypotheses of
acoustically mediated bubble growth.''
Although theoretical predictions suggest the possibility for
acoustically mediated bubble growth, there is considerable disagreement
among scientists as to its likelihood (Piantadosi and Thalmann, 2004;
Evans and Miller, 2003). Crum and Mao (1996) hypothesized that received
levels would have to exceed 190 dB in order for there to be the
possibility of significant bubble growth due to supersaturation of
gases in the blood (i.e., rectified diffusion). More recent work
conducted by Crum et al. (2005) demonstrated the possibility of
rectified diffusion for short duration signals, but at SELs and tissue
saturation levels that are highly improbable to occur in diving marine
mammals. To date, energy levels (ELs) predicted to cause in vivo bubble
formation within diving cetaceans have not been evaluated (NOAA,
2002b). Although it has been argued that traumas from some recent
beaked whale strandings are consistent with gas emboli and bubble-
induced tissue separations (Jepson et al., 2003), there is no
conclusive evidence of this. However, Jepson et al. (2003, 2005) and
Fernandez et al. (2004, 2005, 2012) concluded that in vivo bubble
formation, which may be exacerbated by deep, long-duration, repetitive
dives may explain why beaked whales appear to be particularly
vulnerable to sonar exposures. Further investigation is needed to
further assess the potential
[[Page 9963]]
validity of these hypotheses. More information regarding hypotheses
that attempt to explain how behavioral responses to non-impulsive
sources can lead to strandings is included in the Stranding and
Mortality section.
Acoustic Masking
Marine mammals use acoustic signals for a variety of purposes,
which differ among species, but include communication between
individuals, navigation, foraging, reproduction, and learning about
their environment (Erbe and Farmer, 2000; Tyack, 2000). Masking, or
auditory interference, generally occurs when sounds in the environment
are louder than and of a similar frequency to, auditory signals an
animal is trying to receive. Masking is a phenomenon that affects
animals that are trying to receive acoustic information about their
environment, including sounds from other members of their species,
predators, prey, and sounds that allow them to orient in their
environment. Masking these acoustic signals can disturb the behavior of
individual animals, groups of animals, or entire populations.
The extent of the masking interference depends on the spectral,
temporal, and spatial relationships between the signals an animal is
trying to receive and the masking noise, in addition to other factors.
In humans, significant masking of tonal signals occurs as a result of
exposure to noise in a narrow band of similar frequencies. As the sound
level increases, though, the detection of frequencies above those of
the masking stimulus decreases also. This principle is expected to
apply to marine mammals as well because of common biomechanical
cochlear properties across taxa.
Richardson et al. (1995b) argued that the maximum radius of
influence of an industrial noise (including broadband low-frequency
sound transmission) on a marine mammal is the distance from the source
to the point at which the noise can barely be heard. This range is
determined by either the hearing sensitivity of the animal or the
background noise level present. Industrial masking is most likely to
affect some species' ability to detect communication calls and natural
sounds (i.e., surf noise, prey noise, etc.; Richardson et al., 1995).
The echolocation calls of toothed whales are subject to masking by
high-frequency sound. Human data indicate low-frequency sound can mask
high-frequency sounds (i.e., upward masking). Studies on captive
odontocetes by Au et al. (1974, 1985, 1993) indicate that some species
may use various processes to reduce masking effects (e.g., adjustments
in echolocation call intensity or frequency as a function of background
noise conditions). There is also evidence that the directional hearing
abilities of odontocetes are useful in reducing masking at the high-
frequencies these cetaceans use to echolocate, but not at the low-to-
moderate frequencies they use to communicate (Zaitseva et al., 1980). A
recent study by Nachtigall and Supin (2008) showed that false killer
whales adjust their hearing to compensate for ambient sounds and the
intensity of returning echolocation signals.
The functional hearing ranges of mysticetes, odontocetes, and
pinnipeds underwater all encompass the frequencies of the sonar sources
used in the Navy's low-frequency (LF)/MFAS/HFAS training exercises.
Additionally, almost all species' vocal repertoires span across the
frequencies of these sonar sources used by the Navy. The closer the
characteristics of the masking signal to the signal of interest, the
more likely masking is to occur. For hull-mounted sonar, which accounts
for a large number of the takes of marine mammals (because of the
source strength and number of hours it is conducted), the pulse length
and low duty cycle of the MFAS/HFAS signal makes it less likely that
masking would occur as a result.
Impaired Communication
In addition to making it more difficult for animals to perceive
acoustic cues in their environment, anthropogenic sound presents
separate challenges for animals that are vocalizing. When they
vocalize, animals are aware of environmental conditions that affect the
``active space'' of their vocalizations, which is the maximum area
within which their vocalizations can be detected before it drops to the
level of ambient noise (Brenowitz, 2004; Brumm et al., 2004; Lohr et
al., 2003). Animals are also aware of environmental conditions that
affect whether listeners can discriminate and recognize their
vocalizations from other sounds, which is more important than simply
detecting that a vocalization is occurring (Brenowitz, 1982; Brumm et
al., 2004; Dooling, 2004, Marten and Marler, 1977; Patricelli et al.,
2006). Most animals that vocalize have evolved with an ability to make
adjustments to their vocalizations to increase the signal-to-noise
ratio, active space, and recognizability/distinguishability of their
vocalizations in the face of temporary changes in background noise
(Brumm et al., 2004; Patricelli et al., 2006). Vocalizing animals can
make adjustments to vocalization characteristics such as the frequency
structure, amplitude, temporal structure, and temporal delivery.
Many animals will combine several of these strategies to compensate
for high levels of background noise. Anthropogenic sounds that reduce
the signal-to-noise ratio of animal vocalizations, increase the masked
auditory thresholds of animals listening for such vocalizations, or
reduce the active space of an animal's vocalizations impair
communication between animals. Most animals that vocalize have evolved
strategies to compensate for the effects of short-term or temporary
increases in background or ambient noise on their songs or calls.
Although the fitness consequences of these vocal adjustments remain
unknown, like most other trade-offs animals must make, some of these
strategies probably come at a cost (Patricelli et al., 2006). For
example, vocalizing more loudly in noisy environments may have
energetic costs that decrease the net benefits of vocal adjustment and
alter a bird's energy budget (Brumm, 2004; Wood and Yezerinac, 2006).
Shifting songs and calls to higher frequencies may also impose
energetic costs (Lambrechts, 1996).
Stress Responses
Classic stress responses begin when an animal's central nervous
system perceives a potential threat to its homeostasis. That perception
triggers stress responses regardless of whether a stimulus actually
threatens the animal; the mere perception of a threat is sufficient to
trigger a stress response (Moberg, 2000; Sapolsky et al., 2005; Seyle,
1950). Once an animal's central nervous system perceives a threat, it
mounts a biological response or defense that consists of a combination
of the four general biological defense responses: Behavioral responses,
autonomic nervous system responses, neuroendocrine responses, or immune
responses.
In the case of many stressors, an animal's first and sometimes most
economical (in terms of biotic costs) response is behavioral avoidance
of the potential stressor or avoidance of continued exposure to a
stressor. An animal's second line of defense to stressors involves the
sympathetic part of the autonomic nervous system and the classical
``fight or flight'' response which includes the cardiovascular system,
the gastrointestinal system, the exocrine glands, and the adrenal
medulla to produce changes in heart rate, blood pressure, and
gastrointestinal activity that humans commonly
[[Page 9964]]
associate with ``stress.'' These responses have a relatively short
duration and may or may not have significant long-term effect on an
animal's welfare.
An animal's third line of defense to stressors involves its
neuroendocrine systems; the system that has received the most study has
been the hypothalmus-pituitary-adrenal system (also known as the HPA
axis in mammals or the hypothalamus-pituitary-interrenal axis in fish
and some reptiles). Unlike stress responses associated with the
autonomic nervous system, virtually all neuro-endocrine functions that
are affected by stress--including immune competence, reproduction,
metabolism, and behavior--are regulated by pituitary hormones. Stress-
induced changes in the secretion of pituitary hormones have been
implicated in failed reproduction (Moberg, 1987; Rivier, 1995), altered
metabolism (Elasser et al., 2000), reduced immune competence (Blecha,
2000), and behavioral disturbance. Increases in the circulation of
glucocorticosteroids (cortisol, corticosterone, and aldosterone in
marine mammals; see Romano et al., 2004) have been equated with stress
for many years.
The primary distinction between stress (which is adaptive and does
not normally place an animal at risk) and distress is the biotic cost
of the response. During a stress response, an animal uses glycogen
stores that can be quickly replenished once the stress is alleviated.
In such circumstances, the cost of the stress response would not pose a
risk to the animal's welfare. However, when an animal does not have
sufficient energy reserves to satisfy the energetic costs of a stress
response, energy resources must be diverted from other biotic function,
which impairs those functions that experience the diversion. For
example, when mounting a stress response diverts energy away from
growth in young animals, those animals may experience stunted growth.
When mounting a stress response diverts energy from a fetus, an
animal's reproductive success and its fitness will suffer. In these
cases, the animals will have entered a pre-pathological or pathological
state which is called ``distress'' (Seyle, 1950) or ``allostatic
loading'' (McEwen and Wingfield, 2003). This pathological state will
last until the animal replenishes its biotic reserves sufficient to
restore normal function. Note that these examples involved a long-term
(days or weeks) stress response exposure to stimuli.
Relationships between these physiological mechanisms, animal
behavior, and the costs of stress responses have also been documented
fairly well through controlled experiments; because this physiology
exists in every vertebrate that has been studied, it is not surprising
that stress responses and their costs have been documented in both
laboratory and free-living animals (for examples see, Holberton et al.,
1996; Hood et al., 1998; Jessop et al., 2003; Krausman et al., 2004;
Lankford et al., 2005; Reneerkens et al., 2002; Thompson and Hamer,
2000). Information has also been collected on the physiological
responses of marine mammals to exposure to anthropogenic sounds (Fair
and Becker, 2000; Romano et al., 2002; Wright et al., 2008). Various
efforts have been undertaken to investigate the impact from vessels
(both whale-watching and general vessel traffic noise), and
demonstrated impacts do occur (Bain, 2002; Erbe, 2002; Noren et al.,
2009; Williams et al., 2006, 2009, 2014a, 2014b; Read et al., 2014;
Rolland et al., 2012; Pirotta et al., 2015). This body of research for
the most part has investigated impacts associated with the presence of
chronic stressors, which differ significantly from the proposed Navy
training activities in the GOA TMAA. For example, in an analysis of
energy costs to killer whales, Williams et al. (2009) suggested that
whale-watching in Canada's Johnstone Strait resulted in lost feeding
opportunities due to vessel disturbance, which could carry higher costs
than other measures of behavioral change might suggest. Ayres et al.
(2012) recently reported on research in the Salish Sea (Washington
state) involving the measurement of southern resident killer whale
fecal hormones to assess two potential threats to the species recovery:
Lack of prey (salmon) and impacts to behavior from vessel traffic.
Ayres et al. (2012) suggested that the lack of prey overshadowed any
population-level physiological impacts on southern resident killer
whales from vessel traffic. Rolland et al. (2012) found that noise
reduction from reduced ship traffic in the Bay of Fundy was associated
with decreased stress in North Atlantic right whales. In a conceptual
model developed by the Population Consequences of Acoustic Disturbance
(PCAD) working group, serum hormones were identified as possible
indicators of behavioral effects that are translated into altered rates
of reproduction and mortality. The Office of Naval Research hosted a
workshop (Effects of Stress on Marine Mammals Exposed to Sound) in 2009
that focused on this very topic (ONR, 2009).
Studies of other marine animals and terrestrial animals would also
lead us to expect some marine mammals to experience physiological
stress responses and, perhaps, physiological responses that would be
classified as ``distress'' upon exposure to high frequency, mid-
frequency and low-frequency sounds. For example, Jansen (1998) reported
on the relationship between acoustic exposures and physiological
responses that are indicative of stress responses in humans (for
example, elevated respiration and increased heart rates). Jones (1998)
reported on reductions in human performance when faced with acute,
repetitive exposures to acoustic disturbance. Trimper et al. (1998)
reported on the physiological stress responses of osprey to low-level
aircraft noise while Krausman et al. (2004) reported on the auditory
and physiological stress responses of endangered Sonoran pronghorn to
military overflights. Smith et al. (2004a, 2004b), for example,
identified noise-induced physiological transient stress responses in
hearing-specialist fish (i.e., goldfish) that accompanied short- and
long-term hearing losses. Welch and Welch (1970) reported physiological
and behavioral stress responses that accompanied damage to the inner
ears of fish and several mammals.
Hearing is one of the primary senses marine mammals use to gather
information about their environment and to communicate with
conspecifics. Although empirical information on the relationship
between sensory impairment (TTS, PTS, and acoustic masking) on marine
mammals remains limited, it seems reasonable to assume that reducing an
animal's ability to gather information about its environment and to
communicate with other members of its species would be stressful for
animals that use hearing as their primary sensory mechanism. Therefore,
we assume that acoustic exposures sufficient to trigger onset PTS or
TTS would be accompanied by physiological stress responses because
terrestrial animals exhibit those responses under similar conditions
(NRC, 2003). More importantly, marine mammals might experience stress
responses at received levels lower than those necessary to trigger
onset TTS. Based on empirical studies of the time required to recover
from stress responses (Moberg, 2000), we also assume that stress
responses are likely to persist beyond the time interval required for
animals to recover from TTS and might result in pathological and pre-
pathological states that would
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be as significant as behavioral responses to TTS.
Behavioral Disturbance
Behavioral responses to sound are highly variable and context-
specific. Many different variables can influence an animal's perception
of and response to (nature and magnitude) an acoustic event. An
animal's prior experience with a sound or sound source affects whether
it is less likely (habituation) or more likely (sensitization) to
respond to certain sounds in the future (animals can also be innately
pre-disposed to respond to certain sounds in certain ways) (Southall et
al., 2007). Related to the sound itself, the perceived nearness of the
sound, bearing of the sound (approaching vs. retreating), similarity of
a sound to biologically relevant sounds in the animal's environment
(i.e., calls of predators, prey, or conspecifics), and familiarity of
the sound may affect the way an animal responds to the sound (Southall
et al., 2007). Individuals (of different age, gender, reproductive
status, etc.) among most populations will have variable hearing
capabilities, and differing behavioral sensitivities to sounds that
will be affected by prior conditioning, experience, and current
activities of those individuals. Often, specific acoustic features of
the sound and contextual variables (i.e., proximity, duration, or
recurrence of the sound or the current behavior that the marine mammal
is engaged in or its prior experience), as well as entirely separate
factors such as the physical presence of a nearby vessel, may be more
relevant to the animal's response than the received level alone.
Ellison et al. (2012) outlined an approach to assessing the effects of
sound on marine mammals that incorporates contextual-based factors.
They recommend considering not just the received level of sound, but
also the activity the animal is engaged in at the time the sound is
received, the nature and novelty of the sound (i.e., is this a new
sound from the animal's perspective), and the distance between the
sound source and the animal. They submit that this ``exposure
context,'' as described, greatly influences the type of behavioral
response exhibited by the animal. This sort of contextual information
is challenging to predict with accuracy for ongoing activities that
occur over large scales and large periods of time. While contextual
elements of this sort are typically not included in calculations to
quantify take, they are often considered qualitatively (where
supporting information is available) in the subsequent analysis that
seeks to assess the likely consequences of sound exposures above a
certain level.
Exposure of marine mammals to sound sources can result in no
response or responses including, but not limited to: Increased
alertness; orientation or attraction to a sound source; vocal
modifications; cessation of feeding; cessation of social interaction;
alteration of movement or diving behavior; habitat abandonment
(temporary or permanent); and, in severe cases, panic, flight,
stampede, or stranding, potentially resulting in death (Southall et
al., 2007). A review of marine mammal responses to anthropogenic sound
was first conducted by Richardson and others in 1995. More recent
reviews (Nowacek et al., 2007; Ellison et al., 2012) address studies
conducted since 1995 and focuses on observations where the received
sound level of the exposed marine mammal(s) was known or could be
estimated. The following sub-sections provide examples of behavioral
responses that provide an idea of the variability in behavioral
responses that would be expected given the differential sensitivities
of marine mammal species to sound and the wide range of potential
acoustic sources to which a marine mammal may be exposed. Estimates of
the types of behavioral responses that could occur for a given sound
exposure should be determined from the literature that is available for
each species, or extrapolated from closely related species when no
information exists.
Flight Response--A flight response is a dramatic change in normal
movement to a directed and rapid movement away from the perceived
location of a sound source. Relatively little information on flight
responses of marine mammals to anthropogenic signals exist, although
observations of flight responses to the presence of predators have
occurred (Connor and Heithaus, 1996). Flight responses have been
speculated as being a component of marine mammal strandings associated
with sonar activities (Evans and England, 2001).
Response to Predator--Evidence suggests that at least some marine
mammals have the ability to acoustically identify potential predators.
For example, harbor seals that reside in the coastal waters off British
Columbia are frequently targeted by certain groups of killer whales,
but not others. The seals discriminate between the calls of threatening
and non-threatening killer whales (Deecke et al., 2002), a capability
that should increase survivorship while reducing the energy required
for attending to and responding to all killer whale calls. The
occurrence of masking or hearing impairment provides a means by which
marine mammals may be prevented from responding to the acoustic cues
produced by their predators. Whether or not this is a possibility
depends on the duration of the masking/hearing impairment and the
likelihood of encountering a predator during the time that predator
cues are impeded.
Diving--Changes in dive behavior can vary widely. They may consist
of increased or decreased dive times and surface intervals as well as
changes in the rates of ascent and descent during a dive. Variations in
dive behavior may reflect interruptions in biologically significant
activities (e.g., foraging) or they may be of little biological
significance. Variations in dive behavior may also expose an animal to
potentially harmful conditions (e.g., increasing the chance of ship-
strike) or may serve as an avoidance response that enhances
survivorship. The impact of a variation in diving resulting from an
acoustic exposure depends on what the animal is doing at the time of
the exposure and the type and magnitude of the response.
Nowacek et al. (2004) reported disruptions of dive behaviors in
foraging North Atlantic right whales when exposed to an alerting
stimulus, an action, they noted, that could lead to an increased
likelihood of ship strike. However, the whales did not respond to
playbacks of either right whale social sounds or vessel noise,
highlighting the importance of the sound characteristics in producing a
behavioral reaction. Conversely, Indo-Pacific humpback dolphins have
been observed to dive for longer periods of time in areas where vessels
were present and/or approaching (Ng and Leung, 2003). In both of these
studies, the influence of the sound exposure cannot be decoupled from
the physical presence of a surface vessel, thus complicating
interpretations of the relative contribution of each stimulus to the
response. Indeed, the presence of surface vessels, their approach, and
speed of approach, seemed to be significant factors in the response of
the Indo-Pacific humpback dolphins (Ng and Leung, 2003). Low frequency
signals of the Acoustic Thermometry of Ocean Climate (ATOC) sound
source were not found to affect dive times of humpback whales in
Hawaiian waters (Frankel and Clark, 2000) or to overtly affect elephant
seal dives (Costa et al., 2003). They did, however, produce subtle
effects that varied in direction and degree among the individual seals,
illustrating the equivocal nature of behavioral effects and consequent
[[Page 9966]]
difficulty in defining and predicting them.
Due to past incidents of beaked whale strandings associated with
sonar operations, feedback paths are provided between avoidance and
diving and indirect tissue effects. This feedback accounts for the
hypothesis that variations in diving behavior and/or avoidance
responses can possibly result in nitrogen tissue supersaturation and
nitrogen off-gassing, possibly to the point of deleterious vascular
bubble formation (Jepson et al., 2003). Although hypothetical,
discussions surrounding this potential process are controversial.
Foraging--Disruption of feeding behavior can be difficult to
correlate with anthropogenic sound exposure, so it is usually inferred
by observed displacement from known foraging areas, the appearance of
secondary indicators (e.g., bubble nets or sediment plumes), or changes
in dive behavior. Noise from seismic surveys was not found to impact
the feeding behavior in western grey whales off the coast of Russia
(Yazvenko et al., 2007) and sperm whales engaged in foraging dives did
not abandon dives when exposed to distant signatures of seismic airguns
(Madsen et al., 2006). However, Miller et al. (2009) reported buzz
rates (a proxy for feeding) 19 percent lower during exposure to distant
signatures of seismic airguns. Balaenopterid whales exposed to moderate
low-frequency signals similar to the ATOC sound source demonstrated no
variation in foraging activity (Croll et al., 2001), whereas five out
of six North Atlantic right whales exposed to an acoustic alarm
interrupted their foraging dives (Nowacek et al., 2004). Although the
received sound pressure levels were similar in the latter two studies,
the frequency, duration, and temporal pattern of signal presentation
were different. These factors, as well as differences in species
sensitivity, are likely contributing factors to the differential
response. Blue whales exposed to simulated mid-frequency sonar in the
Southern California Bight were less likely to produce low frequency
calls usually associated with feeding behavior (Melc[oacute]n et al.,
2012). However, Melcon et al. (2012) were unable to determine if
suppression of low frequency calls reflected a change in their feeding
performance or abandonment of foraging behavior and indicated that
implications of the documented responses are unknown. Further, it is
not known whether the lower rates of calling actually indicated a
reduction in feeding behavior or social contact since the study used
data from remotely deployed, passive acoustic monitoring buoys. In
contrast, blue whales increased their likelihood of calling when ship
noise was present, and decreased their likelihood of calling in the
presence of explosive noise, although this result was not statistically
significant (Melc[oacute]n et al., 2012). Additionally, the likelihood
of an animal calling decreased with the increased received level of
mid-frequency sonar, beginning at a SPL of approximately 110-120 dB re
1 [mu]Pa (Melc[oacute]n et al., 2012). Results from the 2010-2011 field
season of an ongoing behavioral response study in Southern California
waters indicated that, in some cases and at low received levels, tagged
blue whales responded to mid-frequency sonar but that those responses
were mild and there was a quick return to their baseline activity
(Southall et al., 2011; Southall et al., 2012b). A determination of
whether foraging disruptions incur fitness consequences will require
information on or estimates of the energetic requirements of the
individuals and the relationship between prey availability, foraging
effort and success, and the life history stage of the animal. Goldbogen
et al., (2013) monitored behavioral responses of tagged blue whales
located in feeding areas when exposed simulated MFA sonar. Responses
varied depending on behavioral context, with deep feeding whales being
more significantly affected (i.e., generalized avoidance; cessation of
feeding; increased swimming speeds; or directed travel away from the
source) compared to surface feeding individuals that typically showed
no change in behavior. Non-feeding whales also seemed to be affected by
exposure. The authors indicate that disruption of feeding and
displacement could impact individual fitness and health. However, for
this to be true, we would have to assume that an individual whale could
not compensate for this lost feeding opportunity by either immediately
feeding at another location, by feeding shortly after cessation of
acoustic exposure, or by feeding at a later time. There is no
indication this is the case, particularly since unconsumed prey would
likely still be available in the environment in most cases following
the cessation of acoustic exposure.
Breathing--Variations in respiration naturally vary with different
behaviors and variations in respiration rate as a function of acoustic
exposure can be expected to co-occur with other behavioral reactions,
such as a flight response or an alteration in diving. However,
respiration rates in and of themselves may be representative of
annoyance or an acute stress response. Mean exhalation rates of gray
whales at rest and while diving were found to be unaffected by seismic
surveys conducted adjacent to the whale feeding grounds (Gailey et al.,
2007). Studies with captive harbor porpoises showed increased
respiration rates upon introduction of acoustic alarms (Kastelein et
al., 2001; Kastelein et al., 2006a) and emissions for underwater data
transmission (Kastelein et al., 2005). However, exposure of the same
acoustic alarm to a striped dolphin under the same conditions did not
elicit a response (Kastelein et al., 2006a), again highlighting the
importance in understanding species differences in the tolerance of
underwater noise when determining the potential for impacts resulting
from anthropogenic sound exposure.
Social Relationships--Social interactions between mammals can be
affected by noise via the disruption of communication signals or by the
displacement of individuals. Disruption of social relationships
therefore depends on the disruption of other behaviors (e.g., caused
avoidance, masking, etc.) and no specific overview is provided here.
However, social disruptions must be considered in context of the
relationships that are affected. Long-term disruptions of mother/calf
pairs or mating displays have the potential to affect the growth and
survival or reproductive effort/success of individuals, respectively.
Vocalizations (also see Masking Section)--Vocal changes in response
to anthropogenic noise can occur across the repertoire of sound
production modes used by marine mammals, such as whistling,
echolocation click production, calling, and singing. Changes may result
in response to a need to compete with an increase in background noise
or may reflect an increased vigilance or startle response. For example,
in the presence of low-frequency active sonar, humpback whales have
been observed to increase the length of their ''songs'' (Miller et al.,
2000; Fristrup et al., 2003), possibly due to the overlap in
frequencies between the whale song and the low-frequency active sonar.
A similar compensatory effect for the presence of low-frequency vessel
noise has been suggested for right whales; right whales have been
observed to shift the frequency content of their calls upward while
reducing the rate of calling in areas of increased anthropogenic noise
(Parks et al., 2007; Roland et al., 2012). Killer whales off the
northwestern coast of the U.S. have been observed to increase the
duration of primary calls once a threshold in
[[Page 9967]]
observing vessel density (e.g., whale watching) was reached, which has
been suggested as a response to increased masking noise produced by the
vessels (Foote et al., 2004; NOAA, 2014b). In contrast, both sperm and
pilot whales potentially ceased sound production during the Heard
Island feasibility test (Bowles et al., 1994), although it cannot be
absolutely determined whether the inability to acoustically detect the
animals was due to the cessation of sound production or the
displacement of animals from the area.
Avoidance--Avoidance is the displacement of an individual from an
area as a result of the presence of a sound. Richardson et al. (1995)
noted that avoidance reactions are the most obvious manifestations of
disturbance in marine mammals. It is qualitatively different from the
flight response, but also differs in the magnitude of the response
(i.e., directed movement, rate of travel, etc.). Oftentimes avoidance
is temporary, and animals return to the area once the noise has ceased.
Longer term displacement is possible, however, which can lead to
changes in abundance or distribution patterns of the species in the
affected region if they do not become acclimated to the presence of the
sound (Blackwell et al., 2004; Bejder et al., 2006; Teilmann et al.,
2006). Acute avoidance responses have been observed in captive
porpoises and pinnipeds exposed to a number of different sound sources
(Kastelein et al., 2001; Finneran et al., 2003; Kastelein et al.,
2006a; Kastelein et al., 2006b). Short-term avoidance of seismic
surveys, low frequency emissions, and acoustic deterrents have also
been noted in wild populations of odontocetes (Bowles et al., 1994;
Goold, 1996; 1998; Stone et al., 2000; Morton and Symonds, 2002) and to
some extent in mysticetes (Gailey et al., 2007), while longer term or
repetitive/chronic displacement for some dolphin groups and for
manatees has been suggested to be due to the presence of chronic vessel
noise (Haviland-Howell et al., 2007; Miksis-Olds et al., 2007).
Maybaum (1993) conducted sound playback experiments to assess the
effects of MFAS on humpback whales in Hawaiian waters. Specifically,
she exposed focal pods to sounds of a 3.3-kHz sonar pulse, a sonar
frequency sweep from 3.1 to 3.6 kHz, and a control (blank) tape while
monitoring behavior, movement, and underwater vocalizations. The two
types of sonar signals (which both contained mid- and low-frequency
components) differed in their effects on the humpback whales, but both
resulted in avoidance behavior. The whales responded to the pulse by
increasing their distance from the sound source and responded to the
frequency sweep by increasing their swimming speeds and track
linearity. In the Caribbean, sperm whales avoided exposure to mid-
frequency submarine sonar pulses, in the range of 1000 Hz to 10,000 Hz
(IWC 2005).
Kvadsheim et al. (2007) conducted a controlled exposure experiment
in which killer whales fitted with D-tags were exposed to mid-frequency
active sonar (Source A: A 1.0 second upsweep 209 dB @ 1-2 kHz every 10
seconds for 10 minutes; Source B: With a 1.0 second upsweep 197 dB @ 6-
7 kHz every 10 seconds for 10 minutes). When exposed to Source A, a
tagged whale and the group it was traveling with did not appear to
avoid the source. When exposed to Source B, the tagged whales along
with other whales that had been carousel feeding, ceased feeding during
the approach of the sonar and moved rapidly away from the source. When
exposed to Source B, Kvadsheim and his co-workers reported that a
tagged killer whale seemed to try to avoid further exposure to the
sound field by the following behaviors: Immediately swimming away
(horizontally) from the source of the sound; engaging in a series of
erratic and frequently deep dives that seemed to take it below the
sound field; or swimming away while engaged in a series of erratic and
frequently deep dives. Although the sample sizes in this study are too
small to support statistical analysis, the behavioral responses of the
killer whales were consistent with the results of other studies.
In 2007, the first in a series of behavioral response studies, a
collaboration by the Navy, NMFS, and other scientists showed one beaked
whale (Mesoplodon densirostris) responding to an MFAS playback. Tyack
et al. (2011) indicates that the playback began when the tagged beaked
whale was vocalizing at depth (at the deepest part of a typical feeding
dive), following a previous control with no sound exposure. The whale
appeared to stop clicking significantly earlier than usual, when
exposed to mid-frequency signals in the 130-140 dB (rms) received level
range. After a few more minutes of the playback, when the received
level reached a maximum of 140-150 dB, the whale ascended on the slow
side of normal ascent rates with a longer than normal ascent, at which
point the exposure was terminated. The results are from a single
experiment and a greater sample size is needed before robust and
definitive conclusions can be drawn.
Tyack et al. (2011) also indicates that Blainville's beaked whales
appear to be sensitive to noise at levels well below expected TTS (~160
dB re1[mu]Pa). This sensitivity is manifest by an adaptive movement
away from a sound source. This response was observed irrespective of
whether the signal transmitted was within the band width of MFAS, which
suggests that beaked whales may not respond to the specific sound
signatures. Instead, they may be sensitive to any pulsed sound from a
point source in this frequency range. The response to such stimuli
appears to involve maximizing the distance from the sound source.
Stimpert et al. (2014) tagged a Baird's beaked whale, which was
subsequently exposed to simulated MFAS. Received levels of sonar on the
tag increased to a maximum of 138 dB re 1[mu]Pa, which occurred during
the first exposure dive. Some sonar received levels could not be
measured due to flow noise and surface noise on the tag.
Results from a 2007-2008 study conducted near the Bahamas showed a
change in diving behavior of an adult Blainville's beaked whale to
playback of MFAS and predator sounds (Boyd et al., 2008; Southall et
al. 2009; Tyack et al., 2011). Reaction to mid-frequency sounds
included premature cessation of clicking and termination of a foraging
dive, and a slower ascent rate to the surface. Results from a similar
behavioral response study in southern California waters have been
presented for the 2010-2011 field season (Southall et al. 2011;
DeRuiter et al., 2013b). DeRuiter et al. (2013b) presented results from
two Cuvier's beaked whales that were tagged and exposed to simulated
MFAS during the 2010 and 2011 field seasons of the southern California
behavioral response study. The 2011 whale was also incidentally exposed
to MFAS from a distant naval exercise. Received levels from the MFAS
signals from the controlled and incidental exposures were calculated as
84-144 and 78-106 dB re 1 [mu]Pa root mean square (rms), respectively.
Both whales showed responses to the controlled exposures, ranging from
initial orientation changes to avoidance responses characterized by
energetic fluking and swimming away from the source. However, the
authors did not detect similar responses to incidental exposure to
distant naval sonar exercises at comparable received levels, indicating
that context of the exposures (e.g., source proximity, controlled
source ramp-up) may have been a significant factor. Specifically, this
result suggests that caution is needed when using marine mammal
response data collected from smaller, nearer sound sources to predict
at what
[[Page 9968]]
received levels animals may repond to larger sound sources that are
significantly farther away--as the distance of the source appears to be
an important contextual variable and animals may be less responsive to
sources at notably greater distances. Cuvier's beaked whale responses
suggested particular sensitivity to sound exposure as consistent with
results for Blainville's beaked whale. Similarly, beaked whales exposed
to sonar during British training exercises stopped foraging (DSTL,
2007), and preliminary results of controlled playback of sonar may
indicate feeding/foraging disruption of killer whales and sperm whales
(Miller et al., 2011).
In the 2007-2008 Bahamas study, playback sounds of a potential
predator--a killer whale--resulted in a similar but more pronounced
reaction, which included longer inter-dive intervals and a sustained
straight-line departure of more than 20 km from the area (Boyd et al.,
2008; Southall et al. 2009; Tyack et al., 2011). The authors noted,
however, that the magnified reaction to the predator sounds could
represent a cumulative effect of exposure to the two sound types since
killer whale playback began approximately 2 hours after mid-frequency
source playback. Pilot whales and killer whales off Norway also
exhibited horizontal avoidance of a transducer with outputs in the mid-
frequency range (signals in the 1-2 kHz and 6-7 kHz ranges) (Miller et
al., 2011). Additionally, separation of a calf from its group during
exposure to MFAS playback was observed on one occasion (Miller et al.,
2011; 2012). Miller et al. (2012) noted that this single observed
mother-calf separation was unusual for several reasons, including the
fact that the experiment was conducted in an unusually narrow fjord
roughly 1 km wide and that the sonar exposure was started unusually
close to the pod including the calf. Both of these factors could have
contributed to calf separation. In contrast, preliminary analyses
suggest that none of the pilot whales or false killer whales in the
Bahamas showed an avoidance response to controlled exposure playbacks
(Southall et al., 2009).
Through analysis of the behavioral response studies, a preliminary
overarching effect of greater sensitivity to all anthropogenic
exposures was seen in beaked whales compared to the other odontocetes
studied (Southall et al., 2009). Therefore, recent studies have focused
specifically on beaked whale responses to active sonar transmissions or
controlled exposure playback of simulated sonar on various military
ranges (Defence Science and Technology Laboratory, 2007; Claridge and
Durban, 2009; Moretti et al., 2009; McCarthy et al., 2011; Miller et
al., 2012; Southall et al., 2011, 2012a, 2012b, 2013, 2014; Tyack et
al., 2011). In the Bahamas, Blainville's beaked whales located on the
range will move off-range during sonar use and return only after the
sonar transmissions have stopped, sometimes taking several days to do
so (Claridge and Durban 2009; Moretti et al., 2009; McCarthy et al.,
2011; Tyack et al., 2011). Moretti et al. (2014) used recordings from
seafloor-mounted hydrophones at the Atlantic Undersea Test and
Evaluation Center (AUTEC) to analyze the probability of Blainsville's
beaked whale dives before, during, and after Navy sonar exercises.
Orientation--A shift in an animal's resting state or an attentional
change via an orienting response represent behaviors that would be
considered mild disruptions if occurring alone. As previously
mentioned, the responses may co-occur with other behaviors; for
instance, an animal may initially orient toward a sound source, and
then move away from it. Thus, any orienting response should be
considered in context of other reactions that may occur.
Behavioral Responses
Southall et al. (2007) reports the results of the efforts of a
panel of experts in acoustic research from behavioral, physiological,
and physical disciplines that convened and reviewed the available
literature on marine mammal hearing and physiological and behavioral
responses to human-made sound with the goal of proposing exposure
criteria for certain effects. This peer-reviewed compilation of
literature is very valuable, though Southall et al. (2007) note that
not all data are equal, some have poor statistical power, insufficient
controls, and/or limited information on received levels, background
noise, and other potentially important contextual variables--such data
were reviewed and sometimes used for qualitative illustration but were
not included in the quantitative analysis for the criteria
recommendations. All of the studies considered, however, contain an
estimate of the received sound level when the animal exhibited the
indicated response.
In the Southall et al. (2007) publication, for the purposes of
analyzing responses of marine mammals to anthropogenic sound and
developing criteria, the authors differentiate between single pulse
sounds, multiple pulse sounds, and non-pulse sounds. MFAS/HFAS sonar is
considered a non-pulse sound. Southall et al. (2007) summarize the
studies associated with low-frequency, mid-frequency, and high-
frequency cetacean and pinniped responses to non-pulse sounds, based
strictly on received level, in Appendix C of their article
(incorporated by reference and summarized in the three paragraphs
below).
The studies that address responses of low-frequency cetaceans to
non-pulse sounds include data gathered in the field and related to
several types of sound sources (of varying similarity to MFAS/HFAS)
including: Vessel noise, drilling and machinery playback, low-frequency
M-sequences (sine wave with multiple phase reversals) playback,
tactical low-frequency active sonar playback, drill ships, Acoustic
Thermometry of Ocean Climate (ATOC) source, and non-pulse playbacks.
These studies generally indicate no (or very limited) responses to
received levels in the 90 to 120 dB re: 1 [mu]Pa range and an
increasing likelihood of avoidance and other behavioral effects in the
120 to 160 dB range. As mentioned earlier, though, contextual variables
play a very important role in the reported responses and the severity
of effects are not linear when compared to received level. Also, few of
the laboratory or field datasets had common conditions, behavioral
contexts or sound sources, so it is not surprising that responses
differ.
The studies that address responses of mid-frequency cetaceans to
non-pulse sounds include data gathered both in the field and the
laboratory and related to several different sound sources (of varying
similarity to MFAS/HFAS) including: Pingers, drilling playbacks, ship
and ice-breaking noise, vessel noise, Acoustic Harassment Devices
(AHDs), Acoustic Deterrent Devices (ADDs), MFAS, and non-pulse bands
and tones. Southall et al. (2007) were unable to come to a clear
conclusion regarding the results of these studies. In some cases,
animals in the field showed significant responses to received levels
between 90 and 120 dB, while in other cases these responses were not
seen in the 120 to 150 dB range. The disparity in results was likely
due to contextual variation and the differences between the results in
the field and laboratory data (animals typically responded at lower
levels in the field).
The studies that address responses of high-frequency cetaceans to
non-pulse sounds include data gathered both in the field and the
laboratory and related to several different sound sources (of varying
similarity to MFAS/HFAS) including: Pingers, AHDs, and various
laboratory non-pulse sounds. All of these data were collected from
harbor
[[Page 9969]]
porpoises. Southall et al. (2007) concluded that the existing data
indicate that harbor porpoises are likely sensitive to a wide range of
anthropogenic sounds at low received levels (~ 90 to 120 dB), at least
for initial exposures. All recorded exposures above 140 dB induced
profound and sustained avoidance behavior in wild harbor porpoises
(Southall et al., 2007). Rapid habituation was noted in some but not
all studies. There is no data to indicate whether other high frequency
cetaceans are as sensitive to anthropogenic sound as harbor porpoises.
The studies that address the responses of pinnipeds in water to
non-impulsive sounds include data gathered both in the field and the
laboratory and related to several different sound sources (of varying
similarity to MFAS/HFAS) including: AHDs, ATOC, various non-pulse
sounds used in underwater data communication, underwater drilling, and
construction noise. Few studies exist with enough information to
include them in the analysis. The limited data suggested that exposures
to non-pulse sounds between 90 and 140 dB generally do not result in
strong behavioral responses in pinnipeds in water, but no data exist at
higher received levels.
Potential Effects of Behavioral Disturbance
The different ways that marine mammals respond to sound are
sometimes indicators of the ultimate effect that exposure to a given
stimulus will have on the well-being (survival, reproduction, etc.) of
an animal. There is limited marine mammal data quantitatively relating
the exposure of marine mammals to sound to effects on reproduction or
survival, though data exists for terrestrial species to which we can
draw comparisons for marine mammals.
Attention is the cognitive process of selectively concentrating on
one aspect of an animal's environment while ignoring other things
(Posner, 1994). Because animals (including humans) have limited
cognitive resources, there is a limit to how much sensory information
they can process at any time. The phenomenon called ``attentional
capture'' occurs when a stimulus (usually a stimulus that an animal is
not concentrating on or attending to) ``captures'' an animal's
attention. This shift in attention can occur consciously or
subconsciously (for example, when an animal hears sounds that it
associates with the approach of a predator) and the shift in attention
can be sudden (Dukas, 2002; van Rij, 2007). Once a stimulus has
captured an animal's attention, the animal can respond by ignoring the
stimulus, assuming a ``watch and wait'' posture, or treat the stimulus
as a disturbance and respond accordingly, which includes scanning for
the source of the stimulus or ``vigilance'' (Cowlishaw et al., 2004).
Vigilance is normally an adaptive behavior that helps animals
determine the presence or absence of predators, assess their distance
from conspecifics, or to attend cues from prey (Bednekoff and Lima,
1998; Treves, 2000). Despite those benefits, however, vigilance has a
cost of time; when animals focus their attention on specific
environmental cues, they are not attending to other activities such as
foraging. These costs have been documented best in foraging animals,
where vigilance has been shown to substantially reduce feeding rates
(Saino, 1994; Beauchamp and Livoreil, 1997; Fritz et al., 2002).
Animals will spend more time being vigilant, which may translate to
less time foraging or resting, when disturbance stimuli approach them
more directly, remain at closer distances, have a greater group size
(for example, multiple surface vessels), or when they co-occur with
times that an animal perceives increased risk (for example, when they
are giving birth or accompanied by a calf). Most of the published
literature, however, suggests that direct approaches will increase the
amount of time animals will dedicate to being vigilant. For example,
bighorn sheep and Dall's sheep dedicated more time being vigilant, and
less time resting or foraging, when aircraft made direct approaches
over them (Frid, 2001; Stockwell et al., 1991).
Several authors have established that long-term and intense
disturbance stimuli can cause population declines by reducing the body
condition of individuals that have been disturbed, followed by reduced
reproductive success, reduced survival, or both (Daan et al., 1996;
Madsen, 1994; White, 1983). For example, Madsen (1994) reported that
pink-footed geese in undisturbed habitat gained body mass and had about
a 46-percent reproductive success rate compared with geese in disturbed
habitat (being consistently scared off the fields on which they were
foraging) which did not gain mass and had a 17-percent reproductive
success rate. Similar reductions in reproductive success have been
reported for mule deer disturbed by all-terrain vehicles (Yarmoloy et
al., 1988), caribou disturbed by seismic exploration blasts (Bradshaw
et al., 1998), caribou disturbed by low-elevation military jet-fights
(Luick et al., 1996), and caribou disturbed by low-elevation jet
flights (Harrington and Veitch, 1992). Similarly, a study of elk that
were disturbed experimentally by pedestrians concluded that the ratio
of young to mothers was inversely related to disturbance rate (Phillips
and Alldredge, 2000).
The primary mechanism by which increased vigilance and disturbance
appear to affect the fitness of individual animals is by disrupting an
animal's time budget and, as a result, reducing the time they might
spend foraging and resting (which increases an animal's activity rate
and energy demand). For example, a study of grizzly bears reported that
bears disturbed by hikers reduced their energy intake by an average of
12 kcal/minute (50.2 x 10\3\kJ/minute), and spent energy fleeing or
acting aggressively toward hikers (White et al. 1999). Alternately,
Ridgway et al. (2006) reported that increased vigilance in bottlenose
dolphins exposed to sound over a 5-day period did not cause any sleep
deprivation or stress effects such as changes in cortisol or
epinephrine levels.
Lusseau and Bejder (2007) present data from three long-term studies
illustrating the connections between disturbance from whale-watching
boats and population-level effects in cetaceans. In Sharks Bay
Australia, the abundance of bottlenose dolphins was compared within
adjacent control and tourism sites over three consecutive 4.5-year
periods of increasing tourism levels. Between the second and third time
periods, in which tourism doubled, dolphin abundance decreased by 15
percent in the tourism area and did not change significantly in the
control area. In Fiordland, New Zealand, two populations (Milford and
Doubtful Sounds) of bottlenose dolphins with tourism levels that
differed by a factor of seven were observed and significant increases
in travelling time and decreases in resting time were documented for
both. Consistent short-term avoidance strategies were observed in
response to tour boats until a threshold of disturbance was reached
(average 68 minutes between interactions), after which the response
switched to a longer term habitat displacement strategy. For one
population tourism only occurred in a part of the home range, however,
tourism occurred throughout the home range of the Doubtful Sound
population and once boat traffic increased beyond the 68-minute
threshold (resulting in abandonment of their home range/preferred
habitat), reproductive success drastically decreased (increased
[[Page 9970]]
stillbirths) and abundance decreased significantly (from 67 to 56
individuals in short period). Last, in a study of northern resident
killer whales off Vancouver Island, exposure to boat traffic was shown
to reduce foraging opportunities and increase traveling time. A simple
bioenergetics model was applied to show that the reduced foraging
opportunities equated to a decreased energy intake of 18 percent, while
the increased traveling incurred an increased energy output of 3-4
percent, which suggests that a management action based on avoiding
interference with foraging might be particularly effective.
On a related note, many animals perform vital functions, such as
feeding, resting, traveling, and socializing, on a diel cycle (24-hour
cycle). Substantive behavioral reactions to noise exposure (such as
disruption of critical life functions, displacement, or avoidance of
important habitat) are more likely to be significant if they last more
than one diel cycle or recur on subsequent days (Southall et al.,
2007). Consequently, a behavioral response lasting less than 1 day and
not recurring on subsequent days is not considered particularly severe
unless it could directly affect reproduction or survival (Southall et
al., 2007). Note that there is a difference between multiple-day
substantive behavioral reactions and multiple-day anthropogenic
activities. For example, just because an at-sea exercises last for
multiple days does not necessarily mean that individual animals are
either exposed to those exercises for multiple days or, further,
exposed in a manner resulting in a sustained multiple day substantive
behavioral responses.
In order to understand how the effects of activities may or may not
impact stocks and populations of marine mammals, it is necessary to
understand not only what the likely disturbances are going to be, but
how those disturbances may affect the reproductive success and
survivorship of individuals, and then how those impacts to individuals
translate to population changes. Following on the earlier work of a
committee of the U.S. National Research Council (NRC, 2005), New et al.
(2014), in an effort termed the Potential Consequences of Disturbance
(PCoD), outline an updated conceptual model of the relationships
linking disturbance to changes in behavior and physiology, health,
vital rates, and population dynamics (below). As depicted, behavioral
and physiological changes can either have direct (acute) effects on
vital rates, such as when changes in habitat use or increased stress
levels raise the probability of mother-calf separation or predation, or
they can have indirect and long-term (chronic) effects on vital rates,
such as when changes in time/energy budgets or increased disease
susceptibility affect health, which then affects vital rates (New et
al., 2014). In addition to outlining this general framework and
compiling the relevant literature that supports it, New et al. (2014)
have chosen four example species for which extensive long-term
monitoring data exist (southern elephant seals, North Atlantic right
whales, Ziphidae beaked whales, and bottlenose dolphins) and developed
state-space energetic models that can be used to effectively forecast
longer-term, population-level impacts from behavioral changes. While
these are very specific models with very specific data requirements
that cannot yet be applied broadly to project-specific risk
assessments, they are a critical first step.
Stranding and Mortality
When a live or dead marine mammal swims or floats onto shore and
becomes ``beached'' or incapable of returning to sea, the event is
termed a ``stranding'' (Geraci et al., 1999; Perrin and Geraci, 2002;
Geraci and Lounsbury, 2005; NMFS, 2007). The legal definition for a
stranding within the U.S. can be found in section 410 of the MMPA (16
U.S.C. 1421h).
Marine mammals are known to strand for a variety of reasons, such
as infectious agents, biotoxicosis, starvation, fishery interaction,
ship strike, unusual oceanographic or weather events, sound exposure,
or combinations of these stressors sustained concurrently or in series.
However, the cause or causes of most strandings are unknown (Geraci et
al., 1976; Eaton, 1979, Odell et al., 1980; Best, 1982). Numerous
studies suggest that the physiology, behavior, habitat relationships,
age, or condition of cetaceans may cause them to strand or might pre-
dispose them to strand when exposed to another phenomenon. These
suggestions are consistent with the conclusions of numerous other
studies that have demonstrated that combinations of dissimilar
stressors commonly combine to kill an animal or dramatically reduce its
fitness, even though one exposure without the other does not produce
the same result (Chroussos, 2000; Creel, 2005; DeVries et al., 2003;
Fair and Becker, 2000; Foley et al., 2001; Moberg, 2000; Relyea, 2005a;
2005b, Romero, 2004; Sih et al., 2004). For reference, between 2001 and
2009, there was an annual average of 1,400 cetacean strandings and
4,300 pinniped strandings along the coasts of the continental U.S. and
Alaska (NMFS, 2011).
Several sources have published lists of mass stranding events of
cetaceans in an attempt to identify relationships between those
stranding events and military sonar (Hildebrand, 2004; IWC, 2005;
Taylor et al., 2004). For example, based on a review of stranding
records between 1960 and 1995, the International Whaling Commission
(2005) identified ten mass stranding events of Cuvier's beaked whales
had been reported and one mass stranding of four Baird's beaked whale.
The IWC concluded that, out of eight stranding events reported from the
mid-1980s to the summer of 2003, seven had been coincident with the use
of tactical mid-frequency sonar, one of those seven had been associated
with the use of tactical low-frequency sonar, and the remaining
stranding event had been associated with the use of seismic airguns.
Most of the stranding events reviewed by the International Whaling
Commission involved beaked whales. A mass stranding of Cuvier's beaked
whales in the eastern Mediterranean Sea occurred in 1996 (Frantzis,
1998) and mass stranding events involving Gervais' beaked whales,
Blainville's beaked whales, and Cuvier's beaked whales occurred off the
coast of the Canary Islands in the late 1980s (Simmonds and Lopez-
Jurado, 1991). The stranding events that occurred in the Canary Islands
and Kyparissiakos Gulf in the late 1990s and the Bahamas in 2000 have
been the most intensively-studied mass stranding events and have been
associated with naval maneuvers involving the use of tactical sonar.
Between 1960 and 2006, 48 strandings (68 percent) involved beaked
whales, three (4 percent) involved dolphins, and 14 (20 percent)
involved whale species. Cuvier's beaked whales were involved in the
greatest number of these events (48 or 68 percent), followed by sperm
whales (seven or 10 percent), and Blainville's and Gervais' beaked
whales (four each or 6 percent). Naval activities (not just activities
conducted by the U.S. Navy) that might have involved active sonar are
reported to have coincided with nine or 10 (13 to 14 percent) of those
stranding events. Between the mid-1980s and 2003 (the period reported
by the International Whaling Commission), NMFS identified reports of 44
mass cetacean stranding events of which at least seven were coincident
with naval exercises that were using MFAS.
[[Page 9971]]
Strandings Associated With Impulsive Sound
Silver Strand--During a Navy training event on March 4, 2011 at the
Silver Strand Training Complex in San Diego, California, three or
possibly four dolphins were killed in an explosion. During an
underwater detonation training event, a pod of 100 to 150 long-beaked
common dolphins were observed moving towards the 700-yd (640.1-m)
exclusion zone around the explosive charge, monitored by personnel in a
safety boat and participants in a dive boat. Approximately 5 minutes
remained on a time-delay fuse connected to a single 8.76 lb (3.97 kg)
explosive charge (C-4 and detonation cord). Although the dive boat was
placed between the pod and the explosive in an effort to guide the
dolphins away from the area, that effort was unsuccessful and three
long-beaked common dolphins near the explosion died. In addition to the
three dolphins found dead on March 4, the remains of a fourth dolphin
were discovered on March 7, 2011 near Ocean Beach, California (3 days
later and approximately 11.8 mi. [19 km] from Silver Strand where the
training event occurred), which might also have been related to this
event. Association of the fourth stranding with the training event is
uncertain because dolphins strand on a regular basis in the San Diego
area. Details such as the dolphins' depth and distance from the
explosive at the time of the detonation could not be estimated from the
250 yd (228.6 m) standoff point of the observers in the dive boat or
the safety boat.
These dolphin mortalities are the only known occurrence of a U.S.
Navy training or testing event involving impulsive energy (underwater
detonation) that caused mortality or injury to a marine mammal (of
note, the time-delay firing underwater explosive training activity
implicated in the March 4 incident is not proposed for the training
activities in the GOA Study Area). Despite this being a rare
occurrence, the Navy has reviewed training requirements, safety
procedures, and possible mitigation measures and implemented changes to
reduce the potential for this to occur in the future. Discussions of
procedures associated with underwater explosives training and other
training events are presented in the Proposed Mitigation section.
Kyle of Durness, Scotland--On July 22, 2011 a mass stranding event
involving long-finned pilot whales occurred at Kyle of Durness,
Scotland. An investigation by Brownlow et al. (2015) considered
unexploded ordnance detonation activities at a Ministry of Defense
bombing range, conducted by the Royal Navy prior to and during the
strandings, as a plausible contributing factor in the mass stranding
event. While Brownlow et al. (2015) concluded that the serial
detonations of underwater ordnance were an influential factor in the
mass stranding event (along with presence of a potentially compromised
animal and navigational error in a topographically complex region) they
also suggest that mitigation measures--which included observations from
a zodiac only and by personnel not experienced in marine mammal
observation, among other deficiencies--were likely insufficient to
assess if cetaceans were in the vicinity of the detonations. The
authors also cite information from the Ministry of Defense indicating
``an extraordinarily high level of activity'' (i.e., frequency and
intensity of underwater explosions) on the range in the days leading up
to the stranding.
Strandings Associated With MFAS
Over the past 16 years, there have been five stranding events
coincident with military mid-frequency sonar use in which exposure to
sonar is believed to have been a contributing factor: Greece (1996);
the Bahamas (2000); Madeira (2000); Canary Islands (2002); and Spain
(2006). Additionally, in 2004, during the Rim of the Pacific (RIMPAC)
exercises, between 150 and 200 usually pelagic melon-headed whales
occupied the shallow waters of Hanalei Bay, Kauai, Hawaii for over 28
hours. NMFS determined that MFAS was a plausible, if not likely,
contributing factor in what may have been a confluence of events that
led to the stranding. A number of other stranding events coincident
with the operation of mid-frequency sonar, including the death of
beaked whales or other species (minke whales, dwarf sperm whales, pilot
whales), have been reported; however, the majority have not been
investigated to the degree necessary to determine the cause of the
stranding and only one of these stranding events, the Bahamas (2000),
was associated with exercises conducted by the U.S. Navy. Most
recently, the Independent Scientific Review Panel investigating
potential contributing factors to a 2008 mass stranding of melon-headed
whales in Antsohihy, Madagascar released its final report suggesting
that the stranding was likely initially triggered by an industry
seismic survey. This report suggests that the operation of a commercial
high-powered 12 kHz multi-beam echosounder during an industry seismic
survey was a plausible and likely initial trigger that caused a large
group of melon-headed whales to leave their typical habitat and then
ultimately strand as a result of secondary factors such as
malnourishment and dehydration. The report indicates that the risk of
this particular convergence of factors and ultimate outcome is likely
very low, but recommends that the potential be considered in
environmental planning. Because of the association between tactical
mid-frequency active sonar use and a small number of marine mammal
strandings, the Navy and NMFS have been considering and addressing the
potential for strandings in association with Navy activities for years.
In addition to a suite of mitigation intended to more broadly minimize
impacts to marine mammals, the Navy and NMFS have a detailed Stranding
Response Plan that outlines reporting, communication, and response
protocols intended both to minimize the impacts of, and enhance the
analysis of, any potential stranding in areas where the Navy operates.
Greece (1996)--Twelve Cuvier's beaked whales stranded atypically
(in both time and space) along a 38.2-km strand of the Kyparissiakos
Gulf coast on May 12 and 13, 1996 (Frantzis, 1998). From May 11 through
May 15, the North Atlantic Treaty Organization (NATO) research vessel
Alliance was conducting sonar tests with signals of 600 Hz and 3 kHz
and source levels of 228 and 226 dB re: 1[mu]Pa, respectively (D'Amico
and Verboom, 1998; D'Spain et al., 2006). The timing and location of
the testing encompassed the time and location of the strandings
(Frantzis, 1998).
Necropsies of eight of the animals were performed but were limited
to basic external examination and sampling of stomach contents, blood,
and skin. No ears or organs were collected, and no histological samples
were preserved. No apparent abnormalities or wounds were found.
Examination of photos of the animals, taken soon after their death,
revealed that the eyes of at least four of the individuals were
bleeding. Photos were taken soon after their death (Frantzis, 2004).
Stomach contents contained the flesh of cephalopods, indicating that
feeding had recently taken place (Frantzis, 1998).
All available information regarding the conditions associated with
this stranding event were compiled, and many potential causes were
examined including major pollution events, prominent tectonic activity,
unusual physical or meteorological events,
[[Page 9972]]
magnetic anomalies, epizootics, and conventional military activities
(International Council for the Exploration of the Sea, 2005a). However,
none of these potential causes coincided in time or space with the mass
stranding, or could explain its characteristics (International Council
for the Exploration of the Sea, 2005a). The robust condition of the
animals, plus the recent stomach contents, is inconsistent with
pathogenic causes. In addition, environmental causes can be ruled out
as there were no unusual environmental circumstances or events before
or during this time period and within the general proximity (Frantzis,
2004).
Because of the rarity of this mass stranding of Cuvier's beaked
whales in the Kyparissiakos Gulf (first one in history), the
probability for the two events (the military exercises and the
strandings) to coincide in time and location, while being independent
of each other, was thought to be extremely low (Frantzis, 1998).
However, because full necropsies had not been conducted, and no
abnormalities were noted, the cause of the strandings could not be
precisely determined (Cox et al., 2006). A Bioacoustics Panel convened
by NATO concluded that the evidence available did not allow them to
accept or reject sonar exposures as a causal agent in these stranding
events. The analysis of this stranding event provided support for, but
no clear evidence for, the cause-and-effect relationship of tactical
sonar training activities and beaked whale strandings (Cox et al.,
2006).
Bahamas (2000)--NMFS and the Navy prepared a joint report
addressing the multi-species stranding in the Bahamas in 2000, which
took place within 24 hours of U.S. Navy ships using MFAS as they passed
through the Northeast and Northwest Providence Channels on March 15-16,
2000. The ships, which operated both AN/SQS-53C and AN/SQS-56, moved
through the channel while emitting sonar pings approximately every 24
seconds. Of the 17 cetaceans that stranded over a 36-hr period
(Cuvier's beaked whales, Blainville's beaked whales, minke whales, and
a spotted dolphin), seven animals died on the beach (five Cuvier's
beaked whales, one Blainville's beaked whale, and the spotted dolphin),
while the other 10 were returned to the water alive (though their
ultimate fate is unknown). As discussed in the Bahamas report (DOC/DON,
2001), there is no likely association between the minke whale and
spotted dolphin strandings and the operation of MFAS.
Necropsies were performed on five of the stranded beaked whales.
All five necropsied beaked whales were in good body condition, showing
no signs of infection, disease, ship strike, blunt trauma, or fishery
related injuries, and three still had food remains in their stomachs.
Auditory structural damage was discovered in four of the whales,
specifically bloody effusions or hemorrhaging around the ears.
Bilateral intracochlear and unilateral temporal region subarachnoid
hemorrhage, with blood clots in the lateral ventricles, were found in
two of the whales. Three of the whales had small hemorrhages in their
acoustic fats (located along the jaw and in the melon).
A comprehensive investigation was conducted and all possible causes
of the stranding event were considered, whether they seemed likely at
the outset or not. Based on the way in which the strandings coincided
with ongoing naval activity involving tactical MFAS use, in terms of
both time and geography, the nature of the physiological effects
experienced by the dead animals, and the absence of any other acoustic
sources, the investigation team concluded that MFAS aboard U.S. Navy
ships that were in use during the active sonar exercise in question
were the most plausible source of this acoustic or impulse trauma to
beaked whales. This sound source was active in a complex environment
that included the presence of a surface duct, unusual and steep
bathymetry, a constricted channel with limited egress, intensive use of
multiple, active sonar units over an extended period of time, and the
presence of beaked whales that appear to be sensitive to the
frequencies produced by these active sonars. The investigation team
concluded that the cause of this stranding event was the confluence of
the Navy MFAS and these contributory factors working together, and
further recommended that the Navy avoid operating MFAS in situations
where these five factors would be likely to occur. This report does not
conclude that all five of these factors must be present for a stranding
to occur, nor that beaked whales are the only species that could
potentially be affected by the confluence of the other factors. Based
on this, NMFS believes that the operation of MFAS in situations where
surface ducts exist, or in marine environments defined by steep
bathymetry and/or constricted channels may increase the likelihood of
producing a sound field with the potential to cause cetaceans
(especially beaked whales) to strand, and therefore, suggests the need
for increased vigilance while operating MFAS in these areas, especially
when beaked whales (or potentially other deep divers) are likely
present.
Madeira, Spain (2000)--From May 10-14, 2000, three Cuvier's beaked
whales were found atypically stranded on two islands in the Madeira
archipelago, Portugal (Cox et al., 2006). A fourth animal was reported
floating in the Madeiran waters by fisherman but did not come ashore
(Woods Hole Oceanographic Institution, 2005). Joint NATO amphibious
training peacekeeping exercises involving participants from 17
countries 80 warships, took place in Portugal during May 2-15, 2000.
The bodies of the three stranded whales were examined post mortem
(Woods Hole Oceanographic Institution, 2005), though only one of the
stranded whales was fresh enough (24 hours after stranding) to be
necropsied (Cox et al., 2006). Results from the necropsy revealed
evidence of hemorrhage and congestion in the right lung and both
kidneys (Cox et al., 2006). There was also evidence of intercochlear
and intracranial hemorrhage similar to that which was observed in the
whales that stranded in the Bahamas event (Cox et al., 2006). There
were no signs of blunt trauma, and no major fractures (Woods Hole
Oceanographic Institution, 2005). The cranial sinuses and airways were
found to be clear with little or no fluid deposition, which may
indicate good preservation of tissues (Woods Hole Oceanographic
Institution, 2005).
Several observations on the Madeira stranded beaked whales, such as
the pattern of injury to the auditory system, are the same as those
observed in the Bahamas strandings. Blood in and around the eyes,
kidney lesions, pleural hemorrhages, and congestion in the lungs are
particularly consistent with the pathologies from the whales stranded
in the Bahamas, and are consistent with stress and pressure related
trauma. The similarities in pathology and stranding patterns between
these two events suggest that a similar pressure event may have
precipitated or contributed to the strandings at both sites (Woods Hole
Oceanographic Institution, 2005).
Even though no definitive causal link can be made between the
stranding event and naval exercises, certain conditions may have
existed in the exercise area that, in their aggregate, may have
contributed to the marine mammal strandings (Freitas, 2004): Exercises
were conducted in areas of at least 547 fathoms (1,000 m) depth near a
shoreline where there is a rapid change in bathymetry on the order of
547 to 3,281 fathoms (1,000 to 6,000 m) occurring across a relatively
short
[[Page 9973]]
horizontal distance (Freitas, 2004); multiple ships were operating
around Madeira, though it is not known if MFAS was used, and the
specifics of the sound sources used are unknown (Cox et al., 2006,
Freitas, 2004); and exercises took place in an area surrounded by
landmasses separated by less than 35 nm (65 km) and at least 10 nm (19
km) in length, or in an embayment. Exercises involving multiple ships
employing MFAS near land may produce sound directed towards a channel
or embayment that may cut off the lines of egress for marine mammals
(Freitas, 2004).
Canary Islands, Spain (2002)--The southeastern area within the
Canary Islands is well known for aggregations of beaked whales due to
its ocean depths of greater than 547 fathoms (1,000 m) within a few
hundred meters of the coastline (Fernandez et al., 2005). On September
24, 2002, 14 beaked whales were found stranded on Fuerteventura and
Lanzarote Islands in the Canary Islands (International Council for
Exploration of the Sea, 2005a). Seven whales died, while the remaining
seven live whales were returned to deeper waters (Fernandez et al.,
2005). Four beaked whales were found stranded dead over the next three
days either on the coast or floating offshore. These strandings
occurred within near proximity of an international naval exercise that
utilized MFAS and involved numerous surface warships and several
submarines. Strandings began about 4 hours after the onset of MFAS
activity (International Council for Exploration of the Sea, 2005a;
Fernandez et al., 2005).
Eight Cuvier's beaked whales, one Blainville's beaked whale, and
one Gervais' beaked whale were necropsied, six of them within 12 hours
of stranding (Fernandez et al., 2005). No pathogenic bacteria were
isolated from the carcasses (Jepson et al., 2003). The animals
displayed severe vascular congestion and hemorrhage especially around
the tissues in the jaw, ears, brain, and kidneys, displaying marked
disseminated microvascular hemorrhages associated with widespread fat
emboli (Jepson et al., 2003; International Council for Exploration of
the Sea, 2005a). Several organs contained intravascular bubbles,
although definitive evidence of gas embolism in vivo is difficult to
determine after death (Jepson et al., 2003). The livers of the
necropsied animals were the most consistently affected organ, which
contained macroscopic gas-filled cavities and had variable degrees of
fibrotic encapsulation. In some animals, cavitary lesions had
extensively replaced the normal tissue (Jepson et al., 2003). Stomachs
contained a large amount of fresh and undigested contents, suggesting a
rapid onset of disease and death (Fernandez et al., 2005). Head and
neck lymph nodes were enlarged and congested, and parasites were found
in the kidneys of all animals (Fernandez et al., 2005).
The association of NATO MFAS use close in space and time to the
beaked whale strandings, and the similarity between this stranding
event and previous beaked whale mass strandings coincident with sonar
use, suggests that a similar scenario and causative mechanism of
stranding may be shared between the events. Beaked whales stranded in
this event demonstrated brain and auditory system injuries,
hemorrhages, and congestion in multiple organs, similar to the
pathological findings of the Bahamas and Madeira stranding events. In
addition, the necropsy results of Canary Islands stranding event lead
to the hypothesis that the presence of disseminated and widespread gas
bubbles and fat emboli were indicative of nitrogen bubble formation,
similar to what might be expected in decompression sickness (Jepson et
al., 2003; Fern[aacute]ndez et al., 2005).
Hanalei Bay (2004)--On July 3 and 4, 2004, approximately 150 to 200
melon-headed whales occupied the shallow waters of the Hanalei Bay,
Kaua'i, Hawaii for over 28 hrs. Attendees of a canoe blessing observed
the animals entering the Bay in a single wave formation at 7 a.m. on
July 3, 2004. The animals were observed moving back into the shore from
the mouth of the Bay at 9 a.m. The usually pelagic animals milled in
the shallow bay and were returned to deeper water with human assistance
beginning at 9:30 a.m. on July 4, 2004, and were out of sight by 10:30
a.m.
Only one animal, a calf, was known to have died following this
event. The animal was noted alive and alone in the Bay on the afternoon
of July 4, 2004, and was found dead in the Bay the morning of July 5,
2004. A full necropsy, magnetic resonance imaging, and computerized
tomography examination were performed on the calf to determine the
manner and cause of death. The combination of imaging, necropsy and
histological analyses found no evidence of infectious, internal
traumatic, congenital, or toxic factors. Cause of death could not be
definitively determined, but it is likely that maternal separation,
poor nutritional condition, and dehydration contributed to the final
demise of the animal. Although it is not known when the calf was
separated from its mother, the animals' movement into the Bay and
subsequent milling and re-grouping may have contributed to the
separation or lack of nursing, especially if the maternal bond was weak
or this was an inexperienced mother with her first calf.
Environmental factors, abiotic and biotic, were analyzed for any
anomalous occurrences that would have contributed to the animals
entering and remaining in Hanalei Bay. The Bay's bathymetry is similar
to many other sites within the Hawaiian Island chain and dissimilar to
sites that have been associated with mass strandings in other parts of
the U.S. The weather conditions appeared to be normal for that time of
year with no fronts or other significant features noted. There was no
evidence of unusual distribution, occurrence of predator or prey
species, or unusual harmful algal blooms, although Mobley et al. (2007)
suggested that the full moon cycle that occurred at that time may have
influenced a run of squid into the Bay. Weather patterns and bathymetry
that have been associated with mass strandings elsewhere were not found
to occur in this instance.
The Hanalei event was spatially and temporally correlated with
RIMPAC. Official sonar training and tracking exercises in the Pacific
Missile Range Facility (PMRF) warning area did not commence until
approximately 8 a.m. on July 3 and were thus ruled out as a possible
trigger for the initial movement into the Bay. However, six naval
surface vessels transiting to the operational area on July 2
intermittently transmitted active sonar (for approximately 9 hours
total from 1:15 p.m. to 12:30 a.m.) as they approached from the south.
The potential for these transmissions to have triggered the whales'
movement into Hanalei Bay was investigated. Analyses with the
information available indicated that animals to the south and east of
Kaua'i could have detected active sonar transmissions on July 2, and
reached Hanalei Bay on or before 7 a.m. on July 3. However, data
limitations regarding the position of the whales prior to their arrival
in the Bay, the magnitude of sonar exposure, behavioral responses of
melon-headed whales to acoustic stimuli, and other possible relevant
factors preclude a conclusive finding regarding the role of sonar in
triggering this event. Propagation modeling suggests that transmissions
from sonar use during the July 3 exercise in the PMRF warning area may
have been detectable at the mouth of the Bay. If the animals responded
negatively to these signals, it may have contributed to their continued
presence in the Bay. The U.S.
[[Page 9974]]
Navy ceased all active sonar transmissions during exercises in this
range on the afternoon of July 3. Subsequent to the cessation of sonar
use, the animals were herded out of the Bay.
While causation of this stranding event may never be unequivocally
determined, NMFS consider the active sonar transmissions of July 2-3,
2004, a plausible, if not likely, contributing factor in what may have
been a confluence of events. This conclusion is based on the following:
(1) The evidently anomalous nature of the stranding; (2) its close
spatiotemporal correlation with wide-scale, sustained use of sonar
systems previously associated with stranding of deep-diving marine
mammals; (3) the directed movement of two groups of transmitting
vessels toward the southeast and southwest coast of Kauai; (4) the
results of acoustic propagation modeling and an analysis of possible
animal transit times to the Bay; and (5) the absence of any other
compelling causative explanation. The initiation and persistence of
this event may have resulted from an interaction of biological and
physical factors. The biological factors may have included the presence
of an apparently uncommon, deep-diving cetacean species (and possibly
an offshore, non-resident group), social interactions among the animals
before or after they entered the Bay, and/or unknown predator or prey
conditions. The physical factors may have included the presence of
nearby deep water, multiple vessels transiting in a directed manner
while transmitting active sonar over a sustained period, the presence
of surface sound ducting conditions, and/or intermittent and random
human interactions while the animals were in the Bay.
A separate event involving melon-headed whales and rough-toothed
dolphins took place over the same period of time in the Northern
Mariana Islands (Jefferson et al., 2006), which is several thousand
miles from Hawaii. Some 500 to 700 melon-headed whales came into
Sasanhaya Bay on July 4, 2004, near the island of Rota and then left of
their own accord after 5.5 hours; no known active sonar transmissions
occurred in the vicinity of that event. The Rota incident led to
scientific debate regarding what, if any, relationship the event had to
the simultaneous events in Hawaii and whether they might be related by
some common factor (e.g., there was a full moon on July 2, 2004, as
well as during other melon-headed whale strandings and nearshore
aggregations (Brownell et al., 2009; Lignon et al., 2007; Mobley et
al., 2007). Brownell et al. (2009) compared the two incidents, along
with one other stranding incident at Nuka Hiva in French Polynesia and
normal resting behaviors observed at Palmyra Island, in regard to
physical features in the areas, melon-headed whale behavior, and lunar
cycles. Brownell et al., (2009) concluded that the rapid entry of the
whales into Hanalei Bay, their movement into very shallow water far
from the 100-m contour, their milling behavior (typical pre-stranding
behavior), and their reluctance to leave the bay constituted an unusual
event that was not similar to the events that occurred at Rota (but was
similar to the events at Palmyra), which appear to be similar to
observations of melon-headed whales resting normally at Palmyra Island.
Additionally, there was no correlation between lunar cycle and the
types of behaviors observed in the Brownell et al. (2009) examples.
Spain (2006)--The Spanish Cetacean Society reported an atypical
mass stranding of four beaked whales that occurred January 26, 2006, on
the southeast coast of Spain, near Mojacar (Gulf of Vera) in the
Western Mediterranean Sea. According to the report, two of the whales
were discovered the evening of January 26 and were found to be still
alive. Two other whales were discovered during the day on January 27,
but had already died. The first three animals were located near the
town of Mojacar and the fourth animal was found dead, a few kilometers
north of the first three animals. From January 25-26, 2006, Standing
NATO Response Force Maritime Group Two (five of seven ships including
one U.S. ship under NATO Operational Control) had conducted active
sonar training against a Spanish submarine within 50 nm (93 km) of the
stranding site.
Veterinary pathologists necropsied the two male and two female
Cuvier's beaked whales. According to the pathologists, the most likely
primary cause of this type of beaked whale mass stranding event was
anthropogenic acoustic activities, most probably anti-submarine MFAS
used during the military naval exercises. However, no positive acoustic
link was established as a direct cause of the stranding. Even though no
causal link can be made between the stranding event and naval
exercises, certain conditions may have existed in the exercise area
that, in their aggregate, may have contributed to the marine mammal
strandings (Freitas, 2004): Exercises were conducted in areas of at
least 547 fathoms (1,000 m) depth near a shoreline where there is a
rapid change in bathymetry on the order of 547 to 3,281 fathoms (1,000
to 6,000 m) occurring across a relatively short horizontal distance
(Freitas, 2004); multiple ships (in this instance, five) were operating
MFAS in the same area over extended periods of time (in this case, 20
hours) in close proximity; and exercises took place in an area
surrounded by landmasses, or in an embayment. Exercises involving
multiple ships employing MFAS near land may have produced sound
directed towards a channel or embayment that may have cut off the lines
of egress for the affected marine mammals (Freitas, 2004).
Association Between Mass Stranding Events and Exposure to MFAS
Several authors have noted similarities between some of these
stranding incidents: They occurred in islands or archipelagoes with
deep water nearby, several appeared to have been associated with
acoustic waveguides like surface ducting, and the sound fields created
by ships transmitting MFAS (Cox et al., 2006; D'Spain et al., 2006).
Although Cuvier's beaked whales have been the most common species
involved in these stranding events (81 percent of the total number of
stranded animals), other beaked whales (including Mesoplodon europeaus,
M. densirostris, and Hyperoodon ampullatus) comprise 14 percent of the
total. Other species (Stenella coeruleoalba, Kogia breviceps and
Balaenoptera acutorostrata) have stranded, but in much lower numbers
and less consistently than beaked whales.
Based on the evidence available, however, NMFS cannot determine
whether (a) Cuvier's beaked whale is more prone to injury from high-
intensity sound than other species; (b) their behavioral responses to
sound makes them more likely to strand; or (c) they are more likely to
be exposed to MFAS than other cetaceans (for reasons that remain
unknown). Because the association between active sonar exposures and
marine mammals mass stranding events is not consistent--some marine
mammals strand without being exposed to sonar and some sonar
transmissions are not associated with marine mammal stranding events
despite their co-occurrence--other risk factors or a grouping of risk
factors probably contribute to these stranding events.
Behaviorally Mediated Responses to MFAS That May Lead To Stranding
Although the confluence of Navy MFAS with the other contributory
factors noted in the report was
[[Page 9975]]
identified as the cause of the 2000 Bahamas stranding event, the
specific mechanisms that led to that stranding (or the others) are not
understood, and there is uncertainty regarding the ordering of effects
that led to the stranding. It is unclear whether beaked whales were
directly injured by sound (e.g., acoustically mediated bubble growth,
as addressed above) prior to stranding or whether a behavioral response
to sound occurred that ultimately caused the beaked whales to be
injured and strand.
Although causal relationships between beaked whale stranding events
and active sonar remain unknown, several authors have hypothesized that
stranding events involving these species in the Bahamas and Canary
Islands may have been triggered when the whales changed their dive
behavior in a startled response to exposure to active sonar or to
further avoid exposure (Cox et al., 2006; Rommel et al., 2006). These
authors proposed three mechanisms by which the behavioral responses of
beaked whales upon being exposed to active sonar might result in a
stranding event. These include the following: Gas bubble formation
caused by excessively fast surfacing; remaining at the surface too long
when tissues are supersaturated with nitrogen; or diving prematurely
when extended time at the surface is necessary to eliminate excess
nitrogen. More specifically, beaked whales that occur in deep waters
that are in close proximity to shallow waters (for example, the
``canyon areas'' that are cited in the Bahamas stranding event; see
D'Spain and D'Amico, 2006), may respond to active sonar by swimming
into shallow waters to avoid further exposures and strand if they were
not able to swim back to deeper waters. Second, beaked whales exposed
to active sonar might alter their dive behavior. Changes in their dive
behavior might cause them to remain at the surface or at depth for
extended periods of time which could lead to hypoxia directly by
increasing their oxygen demands or indirectly by increasing their
energy expenditures (to remain at depth) and increase their oxygen
demands as a result. If beaked whales are at depth when they detect a
ping from an active sonar transmission and change their dive profile,
this could lead to the formation of significant gas bubbles, which
could damage multiple organs or interfere with normal physiological
function (Cox et al., 2006; Rommel et al., 2006; Zimmer and Tyack,
2007). Baird et al. (2005) found that slow ascent rates from deep dives
and long periods of time spent within 50 m of the surface were typical
for both Cuvier's and Blainville's beaked whales, the two species
involved in mass strandings related to naval sonar. These two
behavioral mechanisms may be necessary to purge excessive dissolved
nitrogen concentrated in their tissues during their frequent long dives
(Baird et al., 2005). Baird et al. (2005) further suggests that
abnormally rapid ascents or premature dives in response to high-
intensity sonar could indirectly result in physical harm to the beaked
whales, through the mechanisms described above (gas bubble formation or
non-elimination of excess nitrogen).
Because many species of marine mammals make repetitive and
prolonged dives to great depths, it has long been assumed that marine
mammals have evolved physiological mechanisms to protect against the
effects of rapid and repeated decompressions. Although several
investigators have identified physiological adaptations that may
protect marine mammals against nitrogen gas supersaturation (alveolar
collapse and elective circulation; Kooyman et al., 1972; Ridgway and
Howard, 1979), Ridgway and Howard (1979) reported that bottlenose
dolphins that were trained to dive repeatedly had muscle tissues that
were substantially supersaturated with nitrogen gas. Houser et al.
(2001) used these data to model the accumulation of nitrogen gas within
the muscle tissue of other marine mammal species and concluded that
cetaceans that dive deep and have slow ascent or descent speeds would
have tissues that are more supersaturated with nitrogen gas than other
marine mammals. Based on these data, Cox et al. (2006) hypothesized
that a critical dive sequence might make beaked whales more prone to
stranding in response to acoustic exposures. The sequence began with
(1) very deep (to depths as deep as 2 kilometers) and long (as long as
90 minutes) foraging dives; (2) relatively slow, controlled ascents;
and (3) a series of ``bounce'' dives between 100 and 400 m in depth
(also see Zimmer and Tyack, 2007). They concluded that acoustic
exposures that disrupted any part of this dive sequence (for example,
causing beaked whales to spend more time at surface without the bounce
dives that are necessary to recover from the deep dive) could produce
excessive levels of nitrogen supersaturation in their tissues, leading
to gas bubble and emboli formation that produces pathologies similar to
decompression sickness.
Zimmer and Tyack (2007) modeled nitrogen tension and bubble growth
in several tissue compartments for several hypothetical dive profiles
and concluded that repetitive shallow dives (defined as a dive where
depth does not exceed the depth of alveolar collapse, approximately 72
m for Ziphius), perhaps as a consequence of an extended avoidance
reaction to sonar sound, could pose a risk for decompression sickness
and that this risk should increase with the duration of the response.
Their models also suggested that unrealistically rapid ascent rates of
ascent from normal dive behaviors are unlikely to result in
supersaturation to the extent that bubble formation would be expected.
Tyack et al. (2006) suggested that emboli observed in animals exposed
to mid-frequency range sonar (Jepson et al., 2003; Fernandez et al.,
2005; Fern[aacute]ndez et al., 2012) could stem from a behavioral
response that involves repeated dives shallower than the depth of lung
collapse. Given that nitrogen gas accumulation is a passive process
(i.e. nitrogen is metabolically inert), a bottlenose dolphin was
trained to repetitively dive a profile predicted to elevate nitrogen
saturation to the point that nitrogen bubble formation was predicted to
occur. However, inspection of the vascular system of the dolphin via
ultrasound did not demonstrate the formation of asymptomatic nitrogen
gas bubbles (Houser et al., 2007). Baird et al. (2008), in a beaked
whale tagging study off Hawaii, showed that deep dives are equally
common during day or night, but ``bounce dives'' are typically a
daytime behavior, possibly associated with visual predator avoidance.
This may indicate that ``bounce dives'' are associated with something
other than behavioral regulation of dissolved nitrogen levels, which
would be necessary day and night.
If marine mammals respond to a Navy vessel that is transmitting
active sonar in the same way that they might respond to a predator,
their probability of flight responses should increase when they
perceive that Navy vessels are approaching them directly, because a
direct approach may convey detection and intent to capture (Burger and
Gochfeld, 1981, 1990; Cooper, 1997, 1998). The probability of flight
responses should also increase as received levels of active sonar
increase (and the ship is, therefore, closer) and as ship speeds
increase (that is, as approach speeds increase). For example, the
probability of flight responses in Dall's sheep (Ovis dalli dalli)
(Frid 2001a, b), ringed seals (Phoca hispida) (Born et al., 1999),
Pacific brant (Branta bernic nigricans) and Canada geese (B.
Canadensis) increased as a helicopter or
[[Page 9976]]
fixed-wing aircraft approached groups of these animals more directly
(Ward et al., 1999). Bald eagles (Haliaeetus leucocephalus) perched on
trees alongside a river were also more likely to flee from a paddle
raft when their perches were closer to the river or were closer to the
ground (Steidl and Anthony, 1996).
Despite the many theories involving bubble formation (both as a
direct cause of injury (see Acoustically Mediated Bubble Growth
Section) and an indirect cause of stranding (See Behaviorally Mediated
Bubble Growth Section), Southall et al., (2007) summarizes that there
is either scientific disagreement or a lack of information regarding
each of the following important points: (1) Received acoustical
exposure conditions for animals involved in stranding events; (2)
pathological interpretation of observed lesions in stranded marine
mammals; (3) acoustic exposure conditions required to induce such
physical trauma directly; (4) whether noise exposure may cause
behavioral reactions (such as atypical diving behavior) that
secondarily cause bubble formation and tissue damage; and (5) the
extent the post mortem artifacts introduced by decomposition before
sampling, handling, freezing, or necropsy procedures affect
interpretation of observed lesions.
Strandings in the GOA TMAA
Northern Edge--Prior to the start of Northern Edge 2015 (a joint
training exercise in the GOA TMAA hosted by Alaskan Command) and before
Navy vessels were in the Gulf of Alaska, the Navy was informed by NMFS
of various marine mammals found dead in the Gulf of Alaska and that
NMFS was attempting to obtain samples from them. It has been reported
that at least nine drifting and floating fin whales and multiple
pinniped species were found in Gulf of Alaska waters as early as May
23, 2015 between Kodiak Island to Unimak Pass. NMFS is still
investigating these findings but a possible cause referenced has been
an algal bloom. During Northern Edge 2015, two Navy vessels training in
the Gulf of Alaska on separate days encountered a well-decayed whale
carcass. This whale or whales may possibly be the same animal observed
by both ships, and given the stage of decomposition, might have been
one of the floating whales reported by other entities to NMFS before
Northern Edge began. The ships followed Navy reporting procedures and
the information was provided to NMFS to aid in the investigation. There
is no causal connection with Navy activities given the advanced stage
of decomposition and gap of timing of when Navy maritime training
events began.
Impulsive Sources
Underwater explosive detonations send a shock wave and sound energy
through the water and can release gaseous by-products, create an
oscillating bubble, or cause a plume of water to shoot up from the
water surface. The shock wave and accompanying noise are of most
concern to marine animals. Depending on the intensity of the shock wave
and size, location, and depth of the animal, an animal can be injured,
killed, suffer non-lethal physical effects, experience hearing related
effects with or without behavioral responses, or exhibit temporary
behavioral responses or tolerance from hearing the blast sound.
Generally, exposures to higher levels of impulse and pressure levels
would result in greater impacts to an individual animal.
Injuries resulting from a shock wave take place at boundaries
between tissues of different densities. Different velocities are
imparted to tissues of different densities, and this can lead to their
physical disruption. Blast effects are greatest at the gas-liquid
interface (Landsberg, 2000). Gas-containing organs, particularly the
lungs and gastrointestinal tract, are especially susceptible (Goertner,
1982; Hill, 1978; Yelverton et al., 1973). In addition, gas-containing
organs including the nasal sacs, larynx, pharynx, trachea, and lungs
may be damaged by compression/expansion caused by the oscillations of
the blast gas bubble (Reidenberg and Laitman, 2003). Intestinal walls
can bruise or rupture, with subsequent hemorrhage and escape of gut
contents into the body cavity. Less severe gastrointestinal tract
injuries include contusions, petechiae (small red or purple spots
caused by bleeding in the skin), and slight hemorrhaging (Yelverton et
al., 1973).
Because the ears are the most sensitive to pressure, they are the
organs most sensitive to injury (Ketten, 2000). Sound-related damage
associated with sound energy from detonations can be theoretically
distinct from injury from the shock wave, particularly farther from the
explosion. If a noise is audible to an animal, it has the potential to
damage the animal's hearing by causing decreased sensitivity (Ketten,
1995). Sound-related trauma can be lethal or sublethal. Lethal impacts
are those that result in immediate death or serious debilitation in or
near an intense source and are not, technically, pure acoustic trauma
(Ketten, 1995). Sublethal impacts include hearing loss, which is caused
by exposures to perceptible sounds. Severe damage (from the shock wave)
to the ears includes tympanic membrane rupture, fracture of the
ossicles, damage to the cochlea, hemorrhage, and cerebrospinal fluid
leakage into the middle ear. Moderate injury implies partial hearing
loss due to tympanic membrane rupture and blood in the middle ear.
Permanent hearing loss also can occur when the hair cells are damaged
by one very loud event, as well as by prolonged exposure to a loud
noise or chronic exposure to noise. The level of impact from blasts
depends on both an animal's location and, at outer zones, on its
sensitivity to the residual noise (Ketten, 1995).
There have been fewer studies addressing the behavioral effects of
explosives on marine mammals compared to MFAS/HFAS. However, though the
nature of the sound waves emitted from an explosion are different (in
shape and rise time) from MFAS/HFAS, NMFS still anticipates the same
sorts of behavioral responses to result from repeated explosive
detonations (a smaller range of likely less severe responses (i.e., not
rising to the level of MMPA harassment) would be expected to occur as a
result of exposure to a single explosive detonation that was not
powerful enough or close enough to the animal to cause TTS or injury).
Baleen whales have shown a variety of responses to impulse sound
sources, including avoidance, reduced surface intervals, altered
swimming behavior, and changes in vocalization rates (Richardson et
al., 1995; Gordon et al., 2003; Southall, 2007). While most bowhead
whales did not show active avoidance until within 8 km of seismic
vessels (Richardson et al., 1995), some whales avoided vessels by more
than 20 km at received levels as low as 120 dB re 1 [mu]Pa rms.
Additionally, Malme et al. (1988) observed clear changes in diving and
respiration patterns in bowheads at ranges up to 73 km from seismic
vessels, with received levels as low as 125 dB re 1 [mu]Pa.
Gray whales migrating along the U.S. west coast showed avoidance
responses to seismic vessels by 10 percent of animals at 164 dB re 1
[mu]Pa, and by 90 percent of animals at 190 dB re 1 [mu]Pa, with
similar results for whales in the Bering Sea (Malme 1986, 1988). In
contrast, noise from seismic surveys was not found to impact feeding
behavior or exhalation rates while resting or diving in western gray
whales off the coast of Russia (Yazvenko et al., 2007; Gailey et al.,
2007).
[[Page 9977]]
Humpback whales showed avoidance behavior at ranges of 5-8 km from
a seismic array during observational studies and controlled exposure
experiments in western Australia (McCauley, 1998; Todd et al., 1996)
found no clear short-term behavioral responses by foraging humpbacks to
explosions associated with construction operations in Newfoundland, but
did see a trend of increased rates of net entanglement and a shift to a
higher incidence of net entanglement closer to the noise source.
Seismic pulses at average received levels of 131 dB re 1
micropascal squared second ([mu]Pa\2\-s) caused blue whales to increase
call production (Di Iorio and Clark, 2010). In contrast, McDonald et
al. (1995) tracked a blue whale with seafloor seismometers and reported
that it stopped vocalizing and changed its travel direction at a range
of 10 km from the seismic vessel (estimated received level 143 dB re 1
[mu]Pa peak-to-peak). These studies demonstrate that even low levels of
noise received far from the noise source can induce behavioral
responses.
Madsen et al. (2006) and Miller et al. (2009) tagged and monitored
eight sperm whales in the Gulf of Mexico exposed to seismic airgun
surveys. Sound sources were from approximately 2 to 7 nm away from the
whales and based on multipath propagation received levels were as high
as 162 dB SPL re 1 [mu]Pa with energy content greatest between 0.3 and
3.0 kHz (Madsen, 2006). The whales showed no horizontal avoidance,
although the whale that was approached most closely had an extended
resting period and did not resume foraging until the airguns had ceased
firing (Miller et al., 2009). The remaining whales continued to execute
foraging dives throughout exposure; however, swimming movements during
foraging dives were 6 percent lower during exposure than control
periods, suggesting subtle effects of noise on foraging behavior
(Miller et al., 2009). Captive bottlenose dolphins sometimes vocalized
after an exposure to impulse sound from a seismic watergun (Finneran et
al., 2010a).
A review of behavioral reactions by pinnipeds to impulse noise can
be found in Richardson et al. (1995) and Southall et al. (2007).
Blackwell et al. (2004) observed that ringed seals exhibited little or
no reaction to pipe-driving noise with mean underwater levels of 157 dB
re 1 [mu]Pa rms and in air levels of 112 dB re 20 [mu]Pa, suggesting
that the seals had habituated to the noise. In contrast, captive
California sea lions avoided sounds from an impulse source at levels of
165-170 dB re 1 [mu]Pa (Finneran et al., 2003b). Experimentally,
G[ouml]tz and Janik (2011) tested underwater, startle responses to a
startling sound (sound with a rapid rise time and a 93 dB sensation
level [the level above the animal's threshold at that frequency]) and a
non-startling sound (sound with the same level, but with a slower rise
time) in wild-captured gray seals. The animals exposed to the startling
treatment avoided a known food source, whereas animals exposed to the
non-startling treatment did not react or habituated during the exposure
period. The results of this study highlight the importance of the
characteristics of the acoustic signal in an animal's response of
habituation.
Vessels
Ship strikes of cetaceans can cause major wounds, which may lead to
the death of the animal. An animal at the surface could be struck
directly by a vessel, a surfacing animal could hit the bottom of a
vessel, or an animal just below the surface could be cut by a vessel's
propeller. The severity of injuries typically depends on the size and
speed of the vessel (Knowlton and Kraus, 2001; Laist et al., 2001;
Vanderlaan and Taggart, 2007). The most vulnerable marine mammals are
those that spend extended periods of time at the surface in order to
restore oxygen levels within their tissues after deep dives (e.g., the
sperm whale). In addition, some baleen whales, such as the North
Atlantic right whale, seem generally unresponsive to vessel sound,
making them more susceptible to vessel collisions (Nowacek et al.,
2004). These species are primarily large, slow moving whales. Smaller
marine mammals (e.g., bottlenose dolphin) move quickly through the
water column and are often seen riding the bow wave of large ships.
Marine mammal responses to vessels may include avoidance and changes in
dive pattern (NRC, 2003).
An examination of all known ship strikes from all shipping sources
(civilian and military) indicates vessel speed is a principal factor in
whether a vessel strike results in death (Knowlton and Kraus, 2001;
Laist et al., 2001; Jensen and Silber, 2003; Vanderlaan and Taggart,
2007). In assessing records in which vessel speed was known, Laist et
al. (2001) found a direct relationship between the occurrence of a
whale strike and the speed of the vessel involved in the collision. The
authors concluded that most deaths occurred when a vessel was traveling
in excess of 13 knots.
Jensen and Silber (2003) detailed 292 records of known or probable
ship strikes of all large whale species from 1975 to 2002. Of these,
vessel speed at the time of collision was reported for 58 cases. Of
these cases, 39 (or 67 percent) resulted in serious injury or death (19
of those resulted in serious injury as determined by blood in the
water, propeller gashes or severed tailstock, and fractured skull, jaw,
vertebrae, hemorrhaging, massive bruising or other injuries noted
during necropsy and 20 resulted in death). Operating speeds of vessels
that struck various species of large whales ranged from 2 to 51 knots.
The majority (79 percent) of these strikes occurred at speeds of 13
knots or greater. The average speed that resulted in serious injury or
death was 18.6 knots. Pace and Silber (2005) found that the probability
of death or serious injury increased rapidly with increasing vessel
speed. Specifically, the predicted probability of serious injury or
death increased from 45 to 75 percent as vessel speed increased from 10
to 14 knots, and exceeded 90 percent at 17 knots. Higher speeds during
collisions result in greater force of impact and also appear to
increase the chance of severe injuries or death. While modeling studies
have suggested that hydrodynamic forces pulling whales toward the
vessel hull increase with increasing speed (Clyne, 1999; Knowlton et
al., 1995), this is inconsistent with Silber et al. (2010), which
demonstrated that there is no such relationship (i.e., hydrodynamic
forces are independent of speed).
The Jensen and Silber (2003) report notes that the database
represents a minimum number of collisions, because the vast majority
probably goes undetected or unreported. In contrast, Navy vessels are
likely to detect any strike that does occur, and they are required to
report all ship strikes involving marine mammals. Overall, the
percentages of Navy traffic relative to overall large shipping traffic
are very small (on the order of 2 percent).
There are no records of any Navy vessel strikes to marine mammals
during training or testing activities in the Study Area. There have
been Navy vessel strikes of large whales in areas outside the Study
Area, such as Hawaii and Southern California. However, these areas
differ significantly from the Study Area given that both Hawaii and
Southern California have a much higher number of Navy vessel activities
and much higher densities of large whales.
Other efforts have been undertaken to investigate the impact from
vessels (both whale-watching and general vessel traffic noise) and
demonstrated impacts do occur (Bain, 2002; Erbe, 2002; Lusseau, 2009;
Williams et al., 2006, 2009, 2011b, 2013, 2014a, 2014b; Noren
[[Page 9978]]
et al., 2009; Read et al., 2014; Rolland et al., 2012; Pirotta et al.,
2015). This body of research for the most part has investigated impacts
associated with the presence of chronic stressors, which differ
significantly from generally intermittent Navy training and testing
activities. For example, in an analysis of energy costs to killer
whales, Williams et al. (2009) suggested that whale-watching in the
Johnstone Strait resulted in lost feeding opportunities due to vessel
disturbance, which could carry higher costs than other measures of
behavioral change might suggest. Ayres et al. (2012) recently reported
on research in the Salish Sea involving the measurement of southern
resident killer whale fecal hormones to assess two potential threats to
the species recovery: Lack of prey (salmon) and impacts to behavior
from vessel traffic. Ayres et al. (2012) suggested that the lack of
prey overshadowed any population-level physiological impacts on
southern resident killer whales from vessel traffic.
Based on the implementation of Navy mitigation measures and the low
density of Navy ships in the GOA TMAA, NMFS has concluded,
preliminarily, that the probability of a ship strike is very low,
especially for dolphins and porpoises, killer whales, social pelagic
odontocetes and pinnipeds that are highly visible, and/or comparatively
small and maneuverable. Though more probable because of their size,
NMFS also believes that the likelihood of a Navy vessel striking a
mysticete or sperm whale is also low with the implementation of
mitigation measures and the low density of navy ships in the Study
Area. The Navy did not request take from a ship strike, and based on
our preliminary determination, NMFS is not recommending that they
modify their request at this time. However, both NMFS and the Navy are
currently engaged in a Section 7 consultation under the ESA, and that
consultation will further inform our final decision.
Proposed Mitigation
Under section 101(a)(5)(A) of the MMPA, NMFS must set forth the
``permissible methods of taking pursuant to such activity, and other
means of effecting the least practicable adverse impact on such species
or stock and its habitat, paying particular attention to rookeries,
mating grounds, and areas of similar significance.'' NMFS' duty under
this ``least practicable adverse impact'' standard is to prescribe
mitigation reasonably designed to minimize, to the extent practicable,
any adverse population-level impacts, as well as habitat impacts. While
population-level impacts are minimized by reducing impacts on
individual marine mammals, not all takes have a reasonable potential
for translating to population-level impacts. NMFS' objective under the
``least practicable adverse impact'' standard is to design mitigation
targeting those impacts on individual marine mammals that are
reasonably likely to contribute to adverse population-level effects.
The NDAA of 2004 amended the MMPA as it relates to military
readiness activities and the ITA process such that ``least practicable
adverse impact'' shall include consideration of personnel safety,
practicality of implementation, and impact on the effectiveness of the
``military readiness activity.'' The training and testing activities
described in the Navy's LOA application are considered military
readiness activities.
In Conservation Council for Hawaii v. National Marine Fisheries
Service, No. 1:13-cv-00684 (D. Hawaii March 31, 2015), the court stated
that NMFS ``appear[s] to think that [it] satisf[ies] the statutory
`least practicable adverse impact' requirement with a `negligible
impact' finding.'' In light of the court's decision, we take this
opportunity to make clear our position that the ``negligible impact''
and ``least practicable adverse impact'' requirements are distinct,
even though the focus of both is on population-level impacts.
A population-level impact is an impact on the population numbers
(survival) or growth and reproductive rates (recruitment) of a
particular marine mammal species or stock. As we noted in the preamble
to our general MMPA implementing regulations, not every population-
level impact violates the negligible impact requirement. As we
explained, the negligible impact standard does not require a finding
that the anticipated take will have ``no effect'' on population numbers
or growth rates: ``The statutory standard does not require that the
same recovery rate be maintained, rather that no significant effect on
annual rates of recruitment or survival occurs . . . [T]he key factor
is the significance of the level of impact on rates of recruitment or
survival. Only insignificant impacts on long-term population levels and
trends can be treated as negligible.'' See 54 FR 40338, 40341-42
(September 29, 1989). Nevertheless, while insignificant impacts on
population numbers or growth rates may satisfy the negligible impact
requirement, such impacts still must be mitigated, to the extent
practicable, under the ``least practicable adverse impact''
requirement. Thus, the negligible impact and least practicable adverse
impact requirements are clearly distinct, even though both focus on
population-level effects.
Any mitigation measure(s) prescribed by NMFS should be able to
accomplish, have a reasonable likelihood of accomplishing (based on
current science), or contribute to accomplishing one or more of the
general goals listed below:
a. Avoid or minimize injury or death of marine mammals wherever
possible (goals b, c, and d may contribute to this goal).
b. Reduce the numbers of marine mammals (total number or number at
biologically important time or location) exposed to received levels of
MFAS/HFAS, underwater detonations, or other activities expected to
result in the take of marine mammals (this goal may contribute to a,
above, or to reducing harassment takes only).
c. Reduce the number of times (total number or number at
biologically important time or location) individuals would be exposed
to received levels of MFAS/HFAS, underwater detonations, or other
activities expected to result in the take of marine mammals (this goal
may contribute to a, above, or to reducing harassment takes only).
d. Reduce the intensity of exposures (either total number or number
at biologically important time or location) to received levels of MFAS/
HFAS, underwater detonations, or other activities expected to result in
the take of marine mammals (this goal may contribute to a, above, or to
reducing the severity of harassment takes only).
e. Avoid or minimize adverse effects to marine mammal habitat
(including acoustic habitat), paying special attention to the food
base, activities that block or limit passage to or from biologically
important areas, permanent destruction of habitat, or temporary
destruction/disturbance of habitat during a biologically important
time.
f. For monitoring directly related to mitigation--increase the
probability of detecting marine mammals, thus allowing for more
effective implementation of the mitigation (shut-down zone, etc.).
Our final evaluation of measures that meet one or more of the above
goals includes consideration of the following factors in relation to
one another: The manner in which, and the degree to which, the
successful implementation of the mitigation measures is expected to
reduce population-level impacts to marine mammal species and stocks and
impacts to their habitat; the proven or likely efficacy of the
measures; and the practicability of the suite of measures
[[Page 9979]]
for applicant implementation, including consideration of personnel
safety, practicality of implementation, and impact on the effectiveness
of the military readiness activity.
NMFS reviewed the proposed activities and the suite of proposed
mitigation measures as described in the Navy's LOA application to
determine if they would result in the least practicable adverse effect
on marine mammals. NMFS worked with the Navy in the development of the
Navy's initially proposed measures, which are informed by years of
experience and monitoring. Below are the mitigation measures as agreed
upon by the Navy and NMFS. For additional details regarding the Navy's
mitigation measures, see Chapter 5 in the GOA DSEIS/OEIS.
Lookouts
The Navy will have two types of Lookouts for the purposes of
conducting visual observations: Those positioned on ships; and those
positioned ashore, in aircraft, or on small boats. Lookouts positioned
on ships will diligently observe the air and surface of the water. They
will have multiple observation objectives, which include but are not
limited to detecting the presence of biological resources and
recreational or fishing boats, observing the mitigation zones, and
monitoring for vessel and personnel safety concerns.
Due to manning and space restrictions on aircraft, small boats, and
some Navy ships, Lookouts for these platforms may be supplemented by
the aircraft crew or pilot, boat crew, range site personnel, or shore-
side personnel. Lookouts positioned in minimally manned platforms may
be responsible for tasks in addition to observing the air or surface of
the water (e.g., navigation of a helicopter or small boat). However,
all Lookouts will, considering personnel safety, practicality of
implementation, and impact on the effectiveness of the activity, comply
with the observation objectives described above for Lookouts positioned
on ships.
The procedural measures described in the remainder of this section
primarily consist of having Lookouts during specific training
activities.
All personnel standing watch on the bridge, Commanding Officers,
Executive Officers, maritime patrol aircraft aircrews, anti-submarine
warfare helicopter crews, civilian equivalents, and Lookouts will
successfully complete the United States Navy Marine Species Awareness
Training prior to standing watch or serving as a Lookout. Additional
details on the Navy's Marine Species Awareness Training can be found in
the GOA DSEIS/OEIS. The Navy proposes to use one or more Lookouts
during the training activities described below, which are organized by
stressor category.
Non-Impulsive Sound
Hull Mounted Mid-Frequency Active Sonar
The Navy's current Lookout mitigation measures during training
activities involving hull-mounted MFAS include requirements such as the
number of personnel on watch and the manner in which personnel are to
visually search the area in the vicinity of the ongoing activity.
The Navy is proposing to maintain the number of Lookouts currently
implemented for ships using hull-mounted MFAS. Ships using hull-mounted
MFAS sources associated with ASW activities at sea (with the exception
of ships less than 65 ft. [20 m] in length, which are minimally manned)
will have two Lookouts at the forward position. While using hull-
mounted MFAS sources underway, vessels less than 65 ft. [20 m] in
length and ships that are minimally manned will have one Lookout at the
forward position due to space and manning restrictions.
High-Frequency and Non-Hull-Mounted Mid-Frequency Active Sonar
The Navy currently conducts activities using high-frequency and
non-hull-mounted MFAS in the Study Area. Non-hull-mounted MFAS training
activities include the use of aircraft deployed sonobuoys, helicopter
dipping sonar, and submarine sonar. During those activities, the Navy
employs the following mitigation measures regarding Lookout procedures:
Navy aircraft participating in exercises at sea shall
conduct and maintain, when operationally feasible and safe,
surveillance for marine species of concern as long as it does not
violate safety constraints or interfere with the accomplishment of
primary operational duties.
Helicopters shall observe/survey the vicinity of an ASW
training event for 10 minutes before the first deployment of active
(dipping) sonar in the water.
The Navy is proposing to continue using the number of Lookouts
(one) currently implemented for aircraft conducting non-hull-mounted
MFA sonar activities.
Mitigation measures do not currently exist for other high-frequency
active sonar activities associated with ASW, or for new platforms;
therefore, the Navy is proposing to add a new Lookout and other
measures for these activities and on these platforms when conducted in
the Study Area. The recommended measure is provided below.
The Navy will have one Lookout on ships conducting high-frequency
or non-hull mounted mid-frequency active sonar activities associated
with ASW activities at sea.
Explosives and Impulsive Sound
Improved Extended Echo Ranging Sonobuoys
The Navy is not proposing use of Improved Extended Echo Ranging
Sonobuoys during the GOA TMAA training activities.
Explosive Signal Underwater Sound Buoys Using >0.5-2.5 Pound Net
Explosive Weight
Lookout measures do not currently exist for explosive signal
underwater sound (SUS) buoy activities using >0.5-2.5 pound (lb.) net
explosive weight (NEW). The Navy is proposing to add this measure.
Aircraft conducting SUS activities using >0.5-2.5 lb. NEW will have one
Lookout.
Gunnery Exercises--Small-, Medium-, and Large-Caliber Using a Surface
Target
Currently, the Navy employs the following Lookout procedures during
gunnery exercises:
From the intended firing position, trained Lookouts shall
survey the mitigation zone for marine mammals prior to commencement and
during the exercise as long as practicable.
If applicable, target towing vessels shall maintain a
Lookout. If a marine mammal is sighted in the vicinity of the exercise,
the tow vessel shall immediately notify the firing vessel in order to
secure gunnery firing until the area is clear.
The Navy is proposing to continue using the Lookout procedures
currently implemented for this activity. The Navy will have one Lookout
on the vessel or aircraft conducting small-, medium-, or large-caliber
gunnery exercises against a surface target. Towing vessels, if
applicable, shall also maintain one Lookout.
Missile Exercises Using a Surface Target
Currently, the Navy employs the following Lookout procedures during
missile exercises:
Aircraft shall visually survey the target area for marine
mammals. Visual inspection of the target area shall be made by flying
at 1,500 ft. (457 m) or lower, if safe to do so, and at slowest safe
speed.
[[Page 9980]]
Firing or range clearance aircraft must be able to
actually see ordnance impact areas.
The Navy is proposing to continue using the Lookout procedures
currently implemented for this activity. When aircraft are conducting
missile exercises against a surface target, the Navy will have one
Lookout positioned in an aircraft.
Bombing Exercises (Explosive)
Currently, the Navy employs the following Lookout procedures during
bombing exercises:
If surface vessels are involved, Lookouts shall survey for
floating kelp and marine mammals.
Aircraft shall visually survey the target and buffer zone
for marine mammals prior to and during the exercise. The survey of the
impact area shall be made by flying at 1,500 ft. (460 m) or lower, if
safe to do so, and at the slowest safe speed. Release of ordnance
through cloud cover is prohibited: Aircraft must be able to actually
see ordnance impact areas. Survey aircraft should employ most effective
search tactics and capabilities.
The Navy is proposing to (1) continue implementing the current
measures for bombing exercises, and (2) clarify the number of Lookouts
currently implemented for this activity. The Navy will have one Lookout
positioned in an aircraft conducting bombing exercises, and trained
Lookouts in any surface vessels involved.
Weapons Firing Noise During Gunnery Exercises
The Navy is proposing to continue using the number of Lookouts
currently implemented for gunnery exercises. The Navy will have one
Lookout on the ship conducting explosive and non-explosive gunnery
exercises. This may be the same Lookout described for Gunnery
Exercises--Small-, Medium-, and Large-Caliber Using a Surface Target
when that activity is conducted from a ship against a surface target.
Sinking Exercises
The Navy is proposing to continue using the number of Lookouts
currently implemented for this activity. The Navy will have two
Lookouts (one positioned in an aircraft and one on a vessel) during
sinking exercises.
Physical Disturbance and Strike
Vessels
Currently, the Navy employs the following Lookout procedures to
avoid physical disturbance and strike of marine mammals during at-sea
training:
While underway, surface vessels shall have at least two
Lookouts with binoculars; surfaced submarines shall have at least one
Lookout with binoculars. Lookouts already posted for safety of
navigation and man-overboard precautions may be used to fill this
requirement. As part of their regular duties, Lookouts will watch for
and report to the Officer of the Deck the presence of marine mammals.
Consistent with other ongoing Navy Phase 2 training and testing
(NWTT, MITT, AFTT, HSTT), the Navy is proposing to revise the
mitigation measures for this activity as follows: While underway,
vessels will have a minimum of one Lookout.
Non-Explosive Practice Munitions
Gunnery Exercises--Small-, Medium-, and Large-Caliber Using a Surface
Target
Currently, the Navy employs the same mitigation measures for non-
explosive practice munitions--small-, medium-, and large-caliber
gunnery exercises--as described above for Gunnery Exercises--Small-,
Medium-, and Large-Caliber Using a Surface Target.
The Navy is proposing to continue using the number of Lookouts
currently implemented for these activities. The Navy will have one
Lookout during activities involving non-explosive practice munitions
(e.g., small-, medium-, and large-caliber gunnery exercises) against a
surface target.
Missile Exercises Using a Surface Target
Currently, the Navy employs the same mitigation measures for non-
explosive missile exercises (including rockets) using a surface target
as described for Missile Exercises Using a Surface Target (explosive).
The Navy is proposing to continue using the number of Lookouts
currently implemented for these activities. When aircraft are
conducting non-explosive missile exercises (including exercises using
rockets) against a surface target, the Navy will have one Lookout
positioned in an aircraft.
Bombing Exercises
Currently, the Navy employs the same mitigation measures for non-
explosive bombing exercises as described for Bombing Exercises
(Explosive).
The Navy is proposing to continue using the same Lookout procedures
currently implemented for these activities. The Navy will have one
Lookout positioned in an aircraft during non-explosive bombing
exercises, and trained Lookouts in any surface vessels involved.
Mitigation Zones
The Navy proposes to use mitigation zones to reduce the potential
impacts to marine mammals from training activities. Mitigation zones
are measured as the radius from a source. Unique to each activity
category, each radius represents a distance that the Navy will visually
observe to help reduce injury to marine species. Visual detections of
applicable marine species will be communicated immediately to the
appropriate watch station for information dissemination and appropriate
action. If the presence of marine mammals is detected acoustically,
Lookouts posted in aircraft and on surface vessels will increase the
vigilance of their visual surveillance. As a reference, aerial surveys
are typically made by flying at 1,500 ft. (457 m) altitude or lower at
the slowest safe speed.
Many of the proposed activities have mitigation measures that are
currently being implemented, as required by previous environmental
documents or consultations. Most of the current mitigation zones for
activities that involve the use of impulsive and non-impulsive sources
were originally designed to reduce the potential for onset of TTS. For
the GOA DSEIS/OEIS and the LOA application, the Navy updated the
acoustic propagation modeling to incorporate updated hearing threshold
metrics (i.e., upper and lower frequency limits), updated density data
for marine mammals, and factors such as an animal's likely presence at
various depths. An explanation of the acoustic propagation modeling
process can be found in the Determination of Acoustic Effects on Marine
Mammals for the Gulf of Alaska Training Supplemental Environmental
Impact Statement/Overseas Environmental Impact Statement technical
report (Marine Species Modeling Team, 2014).
As a result of the updates to the acoustic propagation modeling, in
some cases the ranges to onset of TTS effects are much larger than
previous model outputs. Due to the ineffectiveness and unacceptable
operational impacts associated with mitigating these large areas, the
Navy is unable to mitigate for onset of TTS for every activity. In this
GOA TMAA analysis, the Navy developed each recommended mitigation zone
to avoid or reduce the potential for onset PTS, out to the predicted
maximum range. In some cases where the ranges to effects are smaller
than previous models estimated, the mitigation zones were adjusted
accordingly to provide consistency
[[Page 9981]]
across the measures. Mitigating to the predicted maximum range to PTS
consequently also mitigates to the predicted maximum range to onset
mortality (1 percent mortality), onset slight lung injury, and onset
slight gastrointestinal tract injury, since the maximum range to
effects for these criteria are shorter than for PTS. Furthermore, in
most cases, the predicted maximum range to PTS also consequently covers
the predicted average range to TTS. Table 8 summarizes the predicted
average range to TTS, average range to PTS, maximum range to PTS, and
recommended mitigation zone for each activity category, based on the
Navy's acoustic propagation modeling results.
The activity-specific mitigation zones are based on the longest
range for all the functional hearing groups. The mitigation zone for a
majority of activities is driven by either the high-frequency cetaceans
or the sea turtles functional hearing groups. Therefore, the mitigation
zones are even more protective for the remaining functional hearing
groups (i.e., low-frequency cetaceans, mid-frequency cetaceans, and
pinnipeds), and likely cover a larger portion of the potential range to
onset of TTS.
This evaluation includes explosive ranges to TTS and the onset of
auditory injury, non-auditory injury, slight lung injury, and
mortality. For every source proposed for use by the Navy, the
recommended mitigation zones included in Table 8 exceed each of these
ranges. In some instances, the Navy recommends mitigation zones that
are larger or smaller than the predicted maximum range to PTS based on
the effectiveness and operational assessments. The recommended
mitigation zones and their associated assessments are provided
throughout the remainder of this section. The recommended measures are
either currently implemented, are modifications of current measures, or
are new measures.
For some activities specified throughout the remainder of this
section, Lookouts may be required to observe for concentrations of
detached floating vegetation (Sargassum or kelp paddies), which are
indicators of potential marine mammal presence within the mitigation
zone. Those specified activities will not commence if floating
vegetation (Sargassum or kelp paddies) is observed within the
mitigation zone prior to the initial start of the activity. If floating
vegetation is observed prior to the initial start of the activity, the
activity will be relocated to an area where no floating vegetation is
observed. Training will not cease as a result of indicators entering
the mitigation zone after activities have commenced. This measure is
intended only for floating vegetation detached from the seafloor.
Table 8--Predicted Ranges to Effects and Recommended Mitigation Zones for Each Activity Category
--------------------------------------------------------------------------------------------------------------------------------------------------------
Representative source Predicted (longest) Predicted (longest) Predicted maximum Recommended
Activity category (bin) \1\ average range to TTS average range to PTS range to PTS mitigation zone
--------------------------------------------------------------------------------------------------------------------------------------------------------
Non-Impulse Sound
--------------------------------------------------------------------------------------------------------------------------------------------------------
Hull-Mounted Mid[dash]Frequency SQS-53 ASW hull- 3,821 yd. (3.5 km) for 100 yd. (91 m) for Not Applicable....... 6 dB power down at
Active Sonar. mounted sonar (MF1). one ping. one ping. 1,000 yd. (914 m); 4
dB power down at 500
yd. (457 m); and
shutdown at 200 yd.
(183 m).
High-Frequency and Non[dash]Hull AQS-22 ASW dipping 230 yd. (210 m) for 20 yd. (18 m) for one Not applicable....... 200 yd. (183 m).
Mounted Mid[dash]Frequency Active sonar (MF4). one ping. ping.
Sonar.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Explosive and Impulse Sound
--------------------------------------------------------------------------------------------------------------------------------------------------------
Signal Underwater Sound (SUS) buoys Explosive sonobuoy 290 yd. (265 m)....... 113 yd. (103 m)...... 309 yd. (283 m)...... 350 yd. (320 m).
using > 0.5-2.5 lb. NEW. (E3).
Gunnery Exercises--Small- and 40 mm projectile (E2). 190 yd. (174 m)....... 83 yd. (76 m)........ 182 yd. (167 m)...... 200 yd. (183 m).
Medium-Caliber (Surface Target).
Gunnery Exercises--Large-Caliber 5 in. projectiles (E5) 453 yd. (414 m)....... 186 yd. (170 m)...... 526 yd. (481 m)...... 600 yd. (549 m).
(Surface Target).
Missile Exercises (Including Maverick missile (E9). 949 yd. (868 m)....... 398 yd. (364 m)...... 699 yd. (639 m)...... 900 yd. (823 m).
Rockets) up to 250 lb. NEW Using a
Surface Target.
Missile Exercises up to 500 lb. NEW Harpoon missile (E10). 1,832 yd. (1.7 km).... 731 yd. (668 m)...... 1,883 yd. (1.7 km)... 2,000 yd. (1.8 km).
(Surface Target).
Bombing Exercises.................. MK-84 2,000 lb. bomb 2,513 yd. (2.3 km).... 991 yd. (906 m)...... 2,474 yd. (2.3 km)... 2,500 yd. (2.3
(E12). km)\2\.
Sinking Exercises.................. Various up to MK-84 2,513 yd. (2.3 km).... 991 yd. (906 m)...... 2,474 yd. (2.3 km)... 2.5 nm \(2)\.
2,000 lb. bomb (E12).
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ This table does not provide an inclusive list of source bins; bins presented here represent the source bin with the largest range to effects within
the given activity category.
\2\ Recommended mitigation zones are larger than the modeled injury zones to account for multiple types of sources or charges being used.
Notes: in = inches, km = kilometers, lb. = pounds, m = meters, nm = nautical miles, PTS = Permanent Threshold Shift, TTS = Temporary Threshold Shift,
yd. = yards
[[Page 9982]]
Non-Impulsive Sound
Hull-Mounted Mid-Frequency Active Sonar
The Navy is proposing to (1) continue implementing the current
measures for MFAS and (2) to clarify the conditions needed to
recommence an activity after a marine mammal has been detected.
Activities that involve the use of hull-mounted MFA sonar will use
Lookouts for visual observation from a ship immediately before and
during the activity. Mitigation zones for these activities involve
powering down the sonar by 6 dB when a marine mammal is sighted within
1,000 yd. (914 m) of the sonar dome, and by an additional 4 dB when
sighted within 500 yd. (457 m) from the source, for a total reduction
of 10 dB. Active transmissions will cease if a marine mammal is sighted
within 200 yd. (183 m). Active transmission will recommence if any one
of the following conditions is met: (1) The animal is observed exiting
the mitigation zone, (2) the animal is thought to have exited the
mitigation zone based on its course and speed, (3) the mitigation zone
has been clear from any additional sightings for a period of 30
minutes, (4) the ship has transited more than 2,000 yd. (1.8 km) beyond
the location of the last sighting, or (5) the ship concludes that
dolphins are deliberately closing in on the ship to ride the ship's bow
wave (and there are no other marine mammal sightings within the
mitigation zone). Active transmission may resume when dolphins are bow
riding because they are out of the main transmission axis of the active
sonar while in the shallow-wave area of the ship bow.
High-Frequency and Non-Hull-Mounted Mid-Frequency Active Sonar
Non-hull-mounted MFA sonar training activities include the use of
aircraft deployed sonobuoys and helicopter dipping sonar. The Navy is
proposing to: (1) Continue implementing the current mitigation measures
for activities currently being executed, such as dipping sonar
activities; (2) extend the implementation of its current mitigation to
all other activities in this category; and (3) clarify the conditions
needed to recommence an activity after a sighting. The recommended
measures are provided below.
Mitigation will include visual observation from a vessel or
aircraft (with the exception of platforms operating at high altitudes)
immediately before and during active transmission within a mitigation
zone of 200 yd. (183 m) from the active sonar source. For activities
involving helicopter deployed dipping sonar, visual observation will
commence 10 minutes before the first deployment of active dipping
sonar. Helicopter dipping and sonobuoy deployment will not begin if
concentrations of floating vegetation (kelp paddies), are observed in
the mitigation zone. If the source can be turned off during the
activity, active transmission will cease if a marine mammal is sighted
within the mitigation zone. Active transmission will recommence if any
one of the following conditions is met: (1) The animal is observed
exiting the mitigation zone, (2) the animal is thought to have exited
the mitigation zone based on its course and speed, (3) the mitigation
zone has been clear from any additional sightings for a period of 10
minutes for an aircraft-deployed source, (4) the mitigation zone has
been clear from any additional sightings for a period of 30 minutes for
a vessel-deployed source, (5) the vessel or aircraft has repositioned
itself more than 400 yd. (370 m) away from the location of the last
sighting, or (6) the vessel concludes that dolphins are deliberately
closing in to ride the vessel's bow wave (and there are no other marine
mammal sightings within the mitigation zone).
Explosives and Impulsive Sound
Explosive Signal Underwater Sound Buoys Using >0.5-2.5 Pound Net
Explosive Weight
Mitigation measures do not currently exist for activities using
explosive signal underwater sound (SUS) buoys.
The Navy is proposing to add the following recommended measures.
Mitigation will include pre-exercise aerial monitoring during
deployment within a mitigation zone of 350 yd. (320 m) around an
explosive SUS buoy. Explosive SUS buoys will not be deployed if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone (around the intended deployment location). SUS
deployment will cease if a marine mammal is sighted within the
mitigation zone. Deployment will recommence if any one of the following
conditions is met: (1) The animal is observed exiting the mitigation
zone, (2) the animal is thought to have exited the mitigation zone
based on its course and speed, or (3) the mitigation zone has been
clear from any additional sightings for a period of 10 minutes.
Passive acoustic monitoring will also be conducted with Navy
assets, such as sonobuoys, already participating in the activity. These
assets would only detect vocalizing marine mammals within the frequency
bands monitored by Navy personnel. Passive acoustic detections would
not provide range or bearing to detected animals, and therefore cannot
provide locations of these animals. Passive acoustic detections would
be reported to Lookouts posted in aircraft in order to increase
vigilance of their visual surveillance.
Gunnery Exercises--Small- and Medium-Caliber Using a Surface Target
The Navy is proposing to (1) continue implementing the current
mitigation measures for this activity, (2) clarify the conditions
needed to recommence an activity after a sighting, and (3) add a
requirement to visually observe for kelp paddies.
Mitigation will include visual observation from a vessel or
aircraft immediately before and during the exercise within a mitigation
zone of 200 yd. (183 m) around the intended impact location. Vessels
will observe the mitigation zone from the firing position. When
aircraft are firing, the aircrew will maintain visual watch of the
mitigation zone during the activity. The exercise will not commence if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone. Firing will cease if a marine mammal is sighted
within the mitigation zone. Firing will recommence if any one of the
following conditions is met: (1) The animal is observed exiting the
mitigation zone, (2) the animal is thought to have exited the
mitigation zone based on its course and speed, (3) the mitigation zone
has been clear from any additional sightings for a period of 10 minutes
for a firing aircraft, (4) the mitigation zone has been clear from any
additional sightings for a period of 30 minutes for a firing ship, or
(5) the intended target location has been repositioned more than 400
yd. (366 m) away from the location of the last sighting.
Gunnery Exercises--Large-Caliber Explosive Rounds Using a Surface
Target
The Navy is proposing to (1) continue using the currently
implemented mitigation zone measures for this activity, (2) clarify the
conditions needed to recommence an activity after a sighting, and (3)
implement a requirement to visually observe for kelp paddies. The
recommended measures are provided below.
Mitigation will include visual observation from a ship immediately
before and during the exercise within a mitigation zone of 600 yd. (549
m) around the intended impact location. Ships will observe the
mitigation zone
[[Page 9983]]
from the firing position. The exercise will not commence if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone. Firing will cease if a marine mammal is sighted
within the mitigation zone. Firing will recommence if any one of the
following conditions is met: (1) The animal is observed exiting the
mitigation zone, (2) the animal is thought to have exited the
mitigation zone based on its course and speed, or (3) the mitigation
zone has been clear from any additional sightings for a period of 30
minutes.
Missile Exercises Up to 250 Pound Net Explosive Weight Using a Surface
Target
Currently, the Navy employs a mitigation zone of 1,800 yd. (1.6 km)
for all missile exercises. Because missiles have a wide range of
warhead strength, the Navy is recommending two mitigation zones; one
for missiles with warheads 250 lb. NEW and less, and a larger
mitigation zone for missiles with larger warheads. The Navy is
proposing to (1) modify the mitigation measures currently implemented
for missile exercises involving missiles with 250 lb. NEW and smaller
warheads by reducing the mitigation zone from 1,800 yd. (1.6 km) to 900
yd. (823 m). This new, reduced mitigation zone is a result of the most
recent acoustic propogation modeling efforts (NAEMO) for the GOA TMAA
and is based on a range to effect that is smaller than previously
modeled for missile exercises using a surface target (as discussed
below, the Navy is proposing to increase the mitigation zone for
missiles with a NEW >250 lb.), (2) clarify the conditions needed to
recommence an activity after a sighting, and (3) adopt the marine
mammal mitigation zone size for floating vegetation for ease of
implementation. The recommended measures are provided below.
When aircraft are involved in the missile firing, mitigation will
include visual observation by the aircrew or supporting aircraft prior
to commencement of the activity within a mitigation zone of 900 yd.
(823 m) around the deployed target. The exercise will not commence if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone. Firing will cease if a marine mammal is sighted
within the mitigation zone. Firing will recommence if any one of the
following conditions is met: (1) The animal is observed exiting the
mitigation zone, (2) the animal is thought to have exited the
mitigation zone based on its course and speed, or (3) the mitigation
zone has been clear from any additional sightings for a period of 10
minutes or 30 minutes (depending on aircraft type).
Missile Exercises 251-500 Pound Net Explosive Weight (Surface Target)
Current mitigation measures apply to all missile exercises,
regardless of the warhead size. The Navy proposes to add a mitigation
zone that applies only to missiles with a NEW of 251 to 500 lb. The
recommended measures are provided below.
When aircraft are involved in the missile firing, mitigation will
include visual observation by the aircrew prior to commencement of the
activity within a mitigation zone of 2,000 yd. (1.8 km) around the
intended impact location. The exercise will not commence if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone. Firing will cease if a marine mammal is sighted
within the mitigation zone. Firing will recommence if any one of the
following conditions is met: (1) The animal is observed exiting the
mitigation zone, (2) the animal is thought to have exited the
mitigation zone based on its course and speed, or (3) the mitigation
zone has been clear from any additional sightings for a period of 10
minutes or 30 minutes (depending on aircraft type).
Bombing Exercises
Currently, the Navy employs the following mitigation zone
procedures during bombing exercises:
Ordnance shall not be targeted to impact within 1,000 yd.
(914 m) of known or observed floating kelp or marine mammals.
A 1,000 yd. (914 m) radius mitigation zone shall be
established around the intended target.
The exercise will be conducted only if marine mammals are
not visible within the mitigation zone.
The Navy is proposing to (1) maintain the existing mitigation zone
to be used for non-explosive bombing activities, (2) revise the
mitigation zone procedures to account for predicted ranges to impacts
to marine species when high explosive bombs are used, (3) clarify the
conditions needed to recommence an activity after a sighting, and (4)
add a requirement to visually observe for kelp paddies.
Mitigation will include visual observation from the aircraft
immediately before the exercise and during target approach within a
mitigation zone of 2,500 yd. (2.3 km) around the intended impact
location for explosive bombs and 1,000 yd. (920 m) for non-explosive
bombs. The exercise will not commence if concentrations of floating
vegetation (kelp paddies) are observed in the mitigation zone. Bombing
will cease if a marine mammal is sighted within the mitigation zone.
Bombing will recommence if any one of the following conditions is met:
(1) The animal is observed exiting the mitigation zone, (2) the animal
is thought to have exited the mitigation zone based on its course and
speed, or (3) the mitigation zone has been clear from any additional
sightings for a period of 10 minutes.
Sinking Exercises
The Navy is proposing to (1) modify the mitigation measures
currently implemented for this activity by increasing the mitigation
zone from 2.0 nm to 2.5 nm, (2) clarify the conditions needed to
recommence an activity after a sighting, (3) add a requirement to
visually observe for kelp paddies, and (4) adopt the marine mammal and
sea turtle mitigation zone size for concentrations of floating
vegetation and aggregations of jellyfish for ease of implementation.
The recommended measures are provided below.
Mitigation will include visual observation within a mitigation zone
of 2.5 nm around the target ship hulk. Sinking exercises will include
aerial observation beginning 90 minutes before the first firing, visual
observations from vessels throughout the duration of the exercise, and
both aerial and vessel observation immediately after any planned or
unplanned breaks in weapons firing of longer than 2 hours. Prior to
conducting the exercise, the Navy will review remotely sensed sea
surface temperature and sea surface height maps to aid in deciding
where to release the target ship hulk.
The Navy will also monitor using passive acoustics during the
exercise. Passive acoustic monitoring would be conducted with Navy
assets, such as passive ships sonar systems or sonobuoys, already
participating in the activity. These assets would only detect
vocalizing marine mammals within the frequency bands monitored by Navy
personnel. Passive acoustic detections would not provide range or
bearing to detected animals, and therefore cannot provide locations of
these animals. Passive acoustic detections would be reported to
Lookouts posted in aircraft and on vessels in order to increase
vigilance of their visual surveillance. Lookouts will also increase
observation vigilance before the use of torpedoes or unguided ordnance
with a NEW of 500 lb. or greater, or if the Beaufort sea state is a 4
or above.
The exercise will not commence if concentrations of floating
vegetation (kelp paddies) are observed in the
[[Page 9984]]
mitigation zone. The exercise will cease if a marine mammal, sea
turtle, or aggregation of jellyfish is sighted within the mitigation
zone. The exercise will recommence if any one of the following
conditions is met: (1) The animal is observed exiting the mitigation
zone, (2) the animal is thought to have exited the mitigation zone
based on a determination of its course and speed and the relative
motion between the animal and the source, or (3) the mitigation zone
has been clear from any additional sightings for a period of 30
minutes. Upon sinking the vessel, the Navy will conduct post-exercise
visual surveillance of the mitigation zone for 2 hours (or until
sunset, whichever comes first).
Weapons Firing Noise During Gunnery Exercises--Large-Caliber
The Navy currently has no mitigation zone procedures for this
activity in the Study Area.
The Navy is proposing to adopt measures currently used during Navy
gunnery exercises in other ranges outside of the Study Area. For all
explosive and non-explosive large-caliber gunnery exercises conducted
from a ship, mitigation will include visual observation immediately
before and during the exercise within a mitigation zone of 70 yd. (46
m) within 30 degrees on either side of the gun target line on the
firing side. The exercise will not commence if concentrations of
floating vegetation (kelp paddies) are observed in the mitigation zone.
Firing will cease if a marine mammal is sighted within the mitigation
zone. Firing will recommence if any one of the following conditions is
met: (1) The animal is observed exiting the mitigation zone, (2) the
animal is thought to have exited the mitigation zone based on its
course and speed, (3) the mitigation zone has been clear from any
additional sightings for a period of 30 minutes, or (4) the vessel has
repositioned itself more than 140 yd. (128 m) away from the location of
the last sighting.
Physical Disturbance and Strike
Vessels
The Navy's current measures to mitigate potential impacts to marine
mammals from vessel and in-water device strikes during training
activities are provided below:
Naval vessels shall maneuver to keep at least 500 yd. (457
m) away from any observed whale in the vessel's path and avoid
approaching whales head-on. These requirements do not apply if a
vessel's safety is threatened, such as when change of course will
create an imminent and serious threat to a person, vessel, or aircraft,
and to the extent vessels are restricted in their ability to maneuver.
Restricted maneuverability includes, but is not limited to, situations
when vessels are engaged in dredging, submerged activities, launching
and recovering aircraft or landing craft, minesweeping activities,
replenishment while underway and towing activities that severely
restrict a vessel's ability to deviate course.
Vessels will take reasonable steps to alert other vessels
in the vicinity of the whale. Given rapid swimming speeds and
maneuverability of many dolphin species, naval vessels would maintain
normal course and speed on sighting dolphins unless some condition
indicated a need for the vessel to maneuver.
The Navy is proposing to continue to use the 500 yd. (457 m) mitigation
zone currently established for whales, and to implement a 200 yd. (183
m) mitigation zone for all other marine mammals. Vessels will avoid
approaching marine mammals head on and will maneuver to maintain a
mitigation zone of 500 yd. (457 m) around observed whales and 200 yd.
(183 m) around all other marine mammals (except bow-riding dolphins),
providing it is safe to do so. The Navy is clarifying its existing
speed protocol; while in transit, Navy vessels shall be alert at all
times, use extreme caution, and proceed at a ``safe speed'' so that the
vessel can take proper and effective action to avoid a collision with
any sighted object or disturbance, including any marine mammal or sea
turtle, and can be stopped within a distance appropriate to the
prevailing circumstances and conditions.
Towed In-Water Devices
The Navy currently has no mitigation zone procedures for this
activity in the Study Area.
The Navy is proposing to adopt measures currently used in other
ranges outside of the Study Area during activities involving towed in-
water devices. The Navy will ensure that towed in-water devices being
towed from manned platforms avoid coming within a mitigation zone of
250 yd. (229 m) around any observed marine mammal, providing it is safe
to do so.
Non-Explosive Practice Munitions
Gunnery Exercises--Small-, Medium-, and Large-Caliber Using a Surface
Target
Currently, the Navy employs the same mitigation measures for non-
explosive gunnery exercises as described above for Gunnery Exercises--
Small-, Medium-, and Large-Caliber Using a Surface Target.
The Navy is proposing to (1) continue using the mitigation measures
currently implemented for this activity, and (2) clarify the conditions
needed to recommence an activity after a sighting. The recommended
measures are provided below.
Mitigation will include visual observation from a vessel or
aircraft immediately before and during the exercise within a mitigation
zone of 200 yd. (183 m) around the intended impact location. The
exercise will not commence if concentrations of floating vegetation
(kelp paddies) are observed in the mitigation zone. Firing will cease
if a marine mammal is sighted within the mitigation zone. Firing will
recommence if any one of the following conditions is met: (1) The
animal is observed exiting the mitigation zone, (2) the animal is
thought to have exited the mitigation zone based on its course and
speed, (3) the mitigation zone has been clear from any additional
sightings for a period of 10 minutes for a firing aircraft, (4) the
mitigation zone has been clear from any additional sightings for a
period of 30 minutes for a firing ship, or (5) the intended target
location has been repositioned more than 400 yd. (366 m) away from the
location of the last sighting.
Bombing Exercises
The Navy is proposing to continue using the mitigation measures
currently implemented for this activity. The recommended measure
includes clarification of a post-sighting activity recommencement
criterion.
Mitigation will include visual observation from the aircraft
immediately before the exercise and during target approach within a
mitigation zone of 1,000 yd. (914 m) around the intended impact
location. The exercise will not commence if concentrations of floating
vegetation (kelp paddies) are observed in the mitigation zone. Bombing
will cease if a marine mammal is sighted within the mitigation zone.
Bombing will recommence if any one of the following conditions is met:
(1) The animal is observed exiting the mitigation zone, (2) the animal
is thought to have exited the mitigation zone based on its course and
speed, or (3) the mitigation zone has been clear from any additional
sightings for a period of 10 minutes.
Missile Exercises (Including Rockets) Using a Surface Target
The Navy is proposing to (1) modify the mitigation measures
currently
[[Page 9985]]
implemented for this activity by reducing the mitigation zone from
1,800 yd. (1.6 km) to 900 yd. (823 m), (2) clarify the conditions
needed to recommence an activity after a sighting, (3) adopt the marine
mammal and sea turtle mitigation zone size for floating vegetation for
ease of implementation, and (4) modify the platform of observation to
eliminate the requirement to observe when ships are firing. The
recommended measures are provided below.
When aircraft are firing, mitigation will include visual
observation by the aircrew or supporting aircraft prior to commencement
of the activity within a mitigation zone of 900 yd. (823 m) around the
deployed target. The exercise will not commence if concentrations of
floating vegetation (kelp paddies) are observed in the mitigation zone.
Firing will cease if a marine mammal is sighted within the mitigation
zone. Firing will recommence if any one of the following conditions is
met: (1) The animal is observed exiting the mitigation zone, (2) the
animal is thought to have exited the mitigation zone based on a
determination of its course and speed and the relative motion between
the animal and the source, or (3) the mitigation zone has been clear
from any additional sightings for a period of 10 minutes or 30 minutes
(depending on aircraft type).
Consideration of Time/Area Limitations
The Navy's and NMFS' analysis of effects to marine mammals
considers emergent science regarding locations where cetaceans are
known to engage in specific activities (e.g., feeding, breeding/
calving, or migration) at certain times of the year that are important
to individual animals as well as populations of marine mammals (see
discussion in Van Parijs, 2015). Where data were available, Van Parijs
(2015) identified areas that are important in this way and named the
areas Biologically Important Areas (BIAs). It is important to note that
the BIAs were not meant to define exclusionary zones, nor were they
meant to be locations that serve as sanctuaries from human activity, or
areas analogous to marine protected areas (see Ferguson et al. (2015a)
regarding the envisioned purpose for the BIA designations). The
delineation of BIAs does not have direct or immediate regulatory
consequences, although it is appropriate to consider them as part of
the body of science that may inform mitigation decisions, depending on
the circumstances. The intention was that the BIAs would serve as
resource management tools and that they be considered along with any
new information as well as, ``existing density estimates, range-wide
distribution data, information on population trends and life history
parameters, known threats to the population, and other relevant
information'' (Van Parijs, 2015).
The Navy and NMFS have supported and will continue to support the
Cetacean and Sound Mapping project, including representation on the
Cetacean Density and distribution Working Group (CetMap), which
informed NMFS' identification of BIAs. The same marine mammal density
data present in the Navy's Marine Species Density Database Technical
Report (U.S. Department of the Navy, 2014) and used in the analysis for
the GOA SEIS/OEIS was used in the development of BIAs. The final
products, including the Gulf of Alaska BIAs, from this mapping effort
were completed and published in March 2015 (Aquatic Mammals, 2015;
Calambokidis et al., 2015; Ferguson et al., 2015a, 2015b; Van Parijs,
2015). 131 BIAs for 24 marine mammal species, stocks, or populations in
seven regions within U.S. waters were identified (Ferguson et al.,
2015a). BIAs have been identified in the Gulf of Alaska in the vicinity
of the GOA TMAA Study Area and include migratory and feeding BIAs for
gray whale and North Pacific right whale, respectively. However, the
degree of overlap between these BIAs and the Study area is negligible
geographically. NMFS' recognition of an area as biologically important
for some species activity is not equivalent to designation of critical
habitat under the Endangered Species Act. Furthermore, the BIAs
identified by NMFS in and around the Study Area do not represent the
totality of important habitat throughout the marine mammals' full
range.
NMFS' Office of Protected Resources routinely considers available
information about marine mammal habitat use to inform discussions with
applicants regarding potential spatio-temporal limitations on their
activities that might help effect the least practicable adverse impact
on species or stocks and their habitat. BIAs are useful tools for
planning and impact assessments and are being provided to the public
via this Web site: www.cetsound.noaa.gov. While these BIAs are useful
tools for analysts, any decisions regarding protective measures based
on these areas must go through the normal MMPA evaluation process (or
any other statutory process that the BIAs are used to inform); the
identification of a BIA does not pre-suppose any specific management
decision associated with those areas, nor does it have direct or
immediate regulatory consequences. NMFS and the Navy have discussed the
BIAs listed above, what Navy activities take place in these areas (in
the context of what their effects on marine mammals might be or whether
additional mitigation is necessary), and what measures could be
implemented to reduce impacts in these areas (in the context of their
potential to reduce marine mammal impacts and their practicability). An
assessment of the potential spatio-temporal and activity overlap of
Navy training activities with the Gulf of Alaska BIAs listed above is
included below and in Chapter 3.8 of the GOA DSEIS/OEIS. In addition,
in the Group and Species-Specific Analysis section of this proposed
rule NMFS has preliminarily assessed the potential effects of Navy
training on the ability of gray whale and North Pacific right whale to
engage in those activities for which the BIAs have been identified
(migratory and feeding). As we learn more about marine mammal density,
distribution, and habitat use (and the BIAs are updated), NMFS and the
Navy will continue to reevaluate appropriate time-area measures through
the Adaptive Management process outlined in these regulations.
North Pacific Right Whale Feeding Area--The NMFS-identified feeding
area for North Pacific right whales (see Ferguson et al., 2015b)
overlaps slightly with the GOA TMAA's southwestern corner. This feeding
area is applicable from June to September so there is temporal overlap
with the proposed Navy training but there is minimal (<1 percent)
spatial overlap between this feeding area and the GOA TMAA (see Figure
3.8-2 of the GOA DSEIS/OEIS).
Given their current extremely low population numbers and the
general lack of sightings in the Gulf of Alaska, the occurrence of
right whales in the GOA TMAA is considered rare. North Pacific right
whales have not been visually detected in the GOA TMAA since at least
the 1960s. The Quinn Seamount passive acoustic detections in summer
2013 ([Scaron]irovi[cacute] et al., 2014) are the only known potential
occurrence records of this species in the GOA TMAA in recent years.
Grey Whale Migratory Area--The NMFS-identified migration area for
gray whales, which was bounded by the extent of the continental shelf
(as provided in Ferguson et al., 2015b), has slight (<1 percent)
overlap with the GOA TMAA at its northernmost corner and western edge
(see Ferguson et al., 2015b; See Figure 3.8-4 of the GOA DSEIS/OEIS).
However, this migration area is applicable only between March to May
(Spring) and November to
[[Page 9986]]
January (Fall) (see Aquatic Mammals, 2015). This NMFS-identified gray
whale migration area would not be applicable during the months when
training has historically occurred (June/July) and is not likely to
have temporal overlap with most of the proposed timeframe (May to
October; summer) for Navy training in the GOA TMAA. It is worth
mentioning that the Navy's acoustic analysis did not predict any takes
of gray whales in the GOA TMAA and NMFS is not authorizing any takes of
this species (see Group and Species-Specific Analysis section later in
this proposed rule).
Potential Training Overlap with BIAs--It is very unlikely that Navy
training would occur in these nearshore locations adjacent to the GOA
TMAA boundary where the overlap with BIAs occurs. To ensure that the
Navy is able to conduct realistic training, Navy units must maintain
sufficient room to maneuver. Therefore, training activities will
typically take place some distance away from an operating area boundary
to ensure sufficient sea or air space is available for tactical
maneuvers within an approved operating area such as the GOA TMAA. The
Navy also does not typically train next to any limiting boundary
because it precludes tactical consideration of the adjacent sea space
and airspace beyond the boundary from being a potential threat axis
during activities such as anti-submarine warfare training. It is also
the case that Navy training activities will generally not be located
where it is likely there would be interference from civilian vessels
and aircraft that are not participating in the training activity. The
nearshore boundary of the GOA TMAA is the location for multiple
commercial vessel transit lanes, ship traffic, and low-altitude air
routes, which all pass through the NMFS-identified feeding area and the
identified migration area (see Figure 3.8-9 of the GOA DSEIS/OEIS).
This level of civilian activity may otherwise conflict with Navy
training activities if those Navy activities were located at that
margin of the GOA TMAA and as a result such an area is generally
avoided.
In short, the corners of and edge of the GOA TMAA are seldom if
ever a suitable location for sustained, realistic, and coordinated
training using sonar and other active acoustic sources or explosives.
The Navy has lookouts and mitigation measures in place to maneuver away
from and around marine mammals, and Navy vessels and aircraft are no
more likely to cause any impact to these species than any other non-
Navy vessels or aircraft in the area. The Navy's stand-off distance for
vessels of 500 yd. (457 m) and mitigation procedures (see Proposed
Mitigation) further reduce the potential that there would be any
biologically meaningful effect to feeding or migration should animals
be present and detected during a very unlikely Navy training event
using sonar and other active acoustic sources or explosives in one of
these overlapping NMFS-identified areas. Therefore, North Pacific right
whales and gray whales in the NMFS-identified feeding or migration
areas at these boundaries of the GOA TMAA are very unlikely to have
their feeding or migration activities affected by Navy training
activities using sonar and other active acoustic sources.
Conclusion--Based on the likely locations for training in the GOA
TMAA, the Navy and NMFS anticipate that proposed training activities
would have very limited, if any, spatial or temporal overlap with the
designated North Pacific right whale area or gray whale biologically
important areas. Therefore, it is unlikely that Navy training would
have any biologically meaningful effect on North Pacific right whale
feeding behavior or gray whale migration behavior in these areas.
Moreover, appropriate mitigation measures (as detailed in Proposed
Mitigation above) would be implemented for any detected marine mammals
and thus further reduce the potential for the feeding or migration
activities to be affected.
Stranding Response Plan
NMFS and the Navy developed a Stranding Response Plan for GOA TMAA
in 2011 as part of the previous (2011-2016) incidental take
authorization and rulemaking process for the Study Area. The Stranding
Response Plan is specifically intended to outline the applicable
requirements in the event that a marine mammal stranding is reported in
the complexes during a major training exercise. NMFS considers all
plausible causes within the course of a stranding investigation and
this plan in no way presumes that any strandings are related to, or
caused by, Navy training activities, absent a determination made during
investigation. The plan is designed to address mitigation, monitoring,
and compliance. The current Stranding Response Plan for the GOA TMAA is
available for review at: https://www.nmfs.noaa.gov/pr/permits/goa_tmaa_stranding_protocol.pdf. NMFS and the Navy are currently
updating the Stranding Response Plan for the GOA TMAA for 2016-2021
training activities. The updated Stranding Response Plan will be
finalized prior to the release of the final rule, and will be made
available for review at: https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm#navy_goa2021. In addition, modifications to the
Stranding Response Plan may also be made through the adaptive
management process.
Mitigation Conclusions
NMFS has carefully evaluated the Navy's proposed mitigation
measures--many of which were developed with NMFS' input during the
first phase of Navy Training authorizations--and considered a broad
range of other measures in the context of ensuring that NMFS prescribes
the means of effecting the least practicable adverse impact on the
affected marine mammal species and stocks and their habitat. Our
evaluation of potential measures included consideration of the
following factors in relation to one another: The manner in which, and
the degree to which, the successful implementation of the mitigation
measures is expected to reduce the likelihood and/or magnitude of
adverse impacts to marine mammal species and stocks and their habitat;
the proven or likely efficacy of the measures; and the practicability
of the suite of measures for applicant implementation, including
consideration of personnel safety, practicality of implementation, and
impact on the effectiveness of the military readiness activity.
Based on our evaluation of the Navy's proposed measures, as well as
other measures considered by NMFS, NMFS has determined preliminarily
that the Navy's proposed mitigation measures (especially when the
adaptive management component is taken into consideration (see Adaptive
Management, below)) are adequate means of effecting the least
practicable adverse impacts on marine mammals species or stocks and
their habitat, paying particular attention to rookeries, mating
grounds, and areas of similar significance, while also considering
personnel safety, practicality of implementation, and impact on the
effectiveness of the military readiness activity.
The proposed rule comment period provides the public an opportunity
to submit recommendations, views, and/or concerns regarding this action
and the proposed mitigation measures. While NMFS has determined
preliminarily that the Navy's proposed mitigation measures would affect
the least practicable adverse impact on the affected species or stocks
and their habitat, NMFS will consider all public comments to help
inform our final
[[Page 9987]]
decision. Consequently, the proposed mitigation measures may be
refined, modified, removed, or added to prior to the issuance of the
final rule based on public comments received, and where appropriate,
further analysis of any additional mitigation measures.
Proposed Monitoring
Section 101(a)(5)(A) of the MMPA states that in order to issue an
ITA for an activity, NMFS must set forth ``requirements pertaining to
the monitoring and reporting of such taking''. The MMPA implementing
regulations at 50 CFR 216.104 (a)(13) indicate that requests for LOAs
must include the suggested means of accomplishing the necessary
monitoring and reporting that will result in increased knowledge of the
species and of the level of taking or impacts on populations of marine
mammals that are expected to be present.
Integrated Comprehensive Monitoring Program (ICMP)
The Navy's ICMP is intended to coordinate monitoring efforts across
all regions and to allocate the most appropriate level and type of
effort for each range complex based on a set of standardized
objectives, and in acknowledgement of regional expertise and resource
availability. The ICMP is designed to be a flexible, scalable, and
adaptable through the adaptive management and strategic planning
processes to periodically assess progress and reevaluate objectives.
Although the ICMP does not specify actual monitoring field work or
projects, it does establish top-level goals that have been developed in
coordination with NMFS. As the ICMP is implemented, detailed and
specific studies will be developed which support the Navy's top-level
monitoring goals. In essence, the ICMP directs that monitoring
activities relating to the effects of Navy training and testing
activities on marine species should be designed to contribute towards
one or more of the following top-level goals:
An increase in our understanding of the likely occurrence
of marine mammals and/or ESA-listed marine species in the vicinity of
the action (i.e., presence, abundance, distribution, and/or density of
species);
An increase in our understanding of the nature, scope, or
context of the likely exposure of marine mammals and/or ESA-listed
species to any of the potential stressor(s) associated with the action
(e.g., tonal and impulsive sound), through better understanding of one
or more of the following: (1) The action and the environment in which
it occurs (e.g., sound source characterization, propagation, and
ambient noise levels); (2) the affected species (e.g., life history or
dive patterns); (3) the likely co-occurrence of marine mammals and/or
ESA-listed marine species with the action (in whole or part) associated
with specific adverse effects, and/or; (4) the likely biological or
behavioral context of exposure to the stressor for the marine mammal
and/or ESA-listed marine species (e.g., age class of exposed animals or
known pupping, calving or feeding areas);
An increase in our understanding of how individual marine
mammals or ESA-listed marine species respond (behaviorally or
physiologically) to the specific stressors associated with the action
(in specific contexts, where possible, e.g., at what distance or
received level);
An increase in our understanding of how anticipated
individual responses, to individual stressors or anticipated
combinations of stressors, may impact either: (1) The long-term fitness
and survival of an individual; or (2) the population, species, or stock
(e.g., through effects on annual rates of recruitment or survival);
An increase in our understanding of the effectiveness of
mitigation and monitoring measures;
A better understanding and record of the manner in which
the authorized entity complies with the ITA and Incidental Take
Statement;
An increase in the probability of detecting marine mammals
(through improved technology or methods), both specifically within the
safety zone (thus allowing for more effective implementation of the
mitigation) and in general, to better achieve the above goals; and
A reduction in the adverse impact of activities to the
least practicable level, as defined in the MMPA.
Monitoring would address the ICMP top-level goals through a
collection of specific regional and ocean basin studies based on
scientific objectives. Quantitative metrics of monitoring effort (e.g.,
20 days of aerial surveys) would not be a specific requirement. The
adaptive management process and reporting requirements would serve as
the basis for evaluating performance and compliance, primarily
considering the quality of the work and results produced, as well as
peer review and publications, and public dissemination of information,
reports, and data. Details of the ICMP are available online (https://www.navymarinespeciesmonitoring. us/).
Strategic Planning Process for Marine Species Monitoring
The Navy also developed the Strategic Planning Process for Marine
Species Monitoring, which establishes the guidelines and processes
necessary to develop, evaluate, and fund individual projects based on
objective scientific study questions. The process uses an underlying
framework designed around top-level goals, a conceptual framework
incorporating a progression of knowledge, and in consultation with a
Scientific Advisory Group and other regional experts. The Strategic
Planning Process for Marine Species Monitoring would be used to set
intermediate scientific objectives, identify potential species of
interest at a regional scale, and evaluate and select specific
monitoring projects to fund or continue supporting for a given fiscal
year. This process would also address relative investments to different
range complexes based on goals across all range complexes, and
monitoring would leverage multiple techniques for data acquisition and
analysis whenever possible. The Strategic Planning Process for Marine
Species Monitoring is also available online (https://www.navymarinespeciesmonitoring navymarinespeciesmonitoring.us/).
Past and Current Monitoring in the Study Area
NMFS has received multiple years' worth of annual exercise and
monitoring reports addressing active sonar use and explosive
detonations within the GOA TMAA and other Navy range complexes. The
data and information contained in these reports have been considered in
developing mitigation and monitoring measures for the proposed training
activities within the Study Area. The Navy's annual exercise and
monitoring reports may be viewed at: https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm and https://www.navymarinespeciesmonitoring.us. NMFS has reviewed these reports and
summarized the results, as related to marine mammal monitoring, below.
1. The Navy has shown significant initiative in developing its
marine species monitoring program and made considerable progress toward
reaching goals and objectives of the ICMP.
2. Observation data from watchstanders aboard navy vessels is
generally useful to indicate the presence or absence of marine mammals
within the mitigation zones (and sometimes beyond) and to document the
implementation of mitigation measures, but does not provide useful
species-specific information or behavioral data.
[[Page 9988]]
3. Data gathered by experienced marine mammal observers can provide
very valuable information at a level of detail not possible with
watchstanders.
4. Though it is by no means conclusive, it is worth noting that no
instances of obvious behavioral disturbance have been observed by Navy
watchstanders or experienced marine mammal observers conducting visual
monitoring.
5. Visual surveys generally provide suitable data for addressing
questions of distribution and abundance of marine mammals, but are much
less effective at providing information on movements and behavior, with
a few notable exceptions where sightings are most frequent.
6. Passive acoustics and animal tagging have significant potential
for applications addressing animal movements and behavioral response to
Navy training activities, but require a longer time horizon and heavy
investment in analysis to produce relevant results.
7. NMFS and the Navy should more carefully consider what and how
information should be gathered by watchstanders during training
exercises and monitoring events, as some reports contain different
information, making cross-report comparisons difficult.
This section is a summary of Navy-funded compliance monitoring in
the GOA TMAA since 2011. Additional Navy-funded monitoring outside of
and in addition to the Navy's commitments to NMFS is provided later in
this section.
Gulf of Alaska Study Area Monitoring, 2011-2015--During the LOA
development process for the 2011 GOA FEIS/OEIS, the Navy and NMFS
agreed that monitoring in the Gulf of Alaska should focus on augmenting
existing baseline data, since regional data on species occurrence and
density are extremely limited. There have been four reports to date
covering work in the Gulf of Alaska (U.S. Department of the Navy,
2011c, 2011d, 2012, 2013f). Collecting baseline data was deemed a
priority prior to focusing on exercise monitoring and behavioral
response as is now being done in other Navy OPAREAs and ranges. There
have been no previous dedicated monitoring efforts during Navy training
activities in the GOA TMAA with the exception of deployed HARPs.
In July 2011, the Navy funded deployment of two long-term bottom-
mounted passive acoustic monitoring buoys by Scripps Institute of
Oceanography. These HARPs were deployed southeast of Kenai Peninsula in
the GOA TMAA with one on the shelf approximately 50 nm from land (in
111 fathoms [203 m] depth) and on the shelf-break slope approximately
100 nm from land (in 492 fathoms [900 m] depth). Intended to be
collected annually, results from the first deployment (July 2011-May
2012) included over 5,756 hours of passive acoustic data (Baumann-
Pickering et al. 2012b). Identification of marine mammal sounds
included four baleen whale species (blue whales, fin whales, gray
whales, and humpback whales) and at least six species of odontocetes
(killer whale, sperm whale, Stejneger's beaked whale, Baird's beaked
whale, Cuvier's beaked whale, and an unidentified porpoise presumed to
be Dall's porpoise; Baumann-Pickering et al., 2012b). Researchers also
noted the detection of anthropogenic sound from commercial shipping.
There were no Navy activities or vessels in the area at any time during
the recording period.
Analysis of the passive acoustic detections made from May 2012 to
June 2013 were presented in Baumann-Pickering et al. (2013), Debich et
al. (2013), Debich et al. (2014), and the Navy's 2012, 2013, and 2014
GOA TMAA annual monitoring report submitted to NMFS (U.S. Department of
the Navy, 2012, 2013f, 2014d). Three baleen whale species were
detected: Blue whales, fin whales, and humpback whales. No North
Pacific right whale calls were detected at either site during this
monitoring period. At least seven species of odontocetes were detected:
Risso's dolphins, killer whales, sperm whales, Baird's beaked whales,
Cuvier's beaked whales, Stejneger's beaked whales, and unidentified
porpoises (likely Dall's porpoise). Focused analysis of beaked whale
echolocation recordings were presented in Baumann-Pickering et al.
(2013).
As also presented in Debich et al. (2013) and U.S. Department of
the Navy (2013f), broadband ship noise was found to be more common at
the slope and Pratt Seamount monitoring sites within the GOA TMAA than
at the nearshore (on shelf) site. Sonar (a variety of frequencies, most
likely fathometers and fish-finders), were more common on the shelf and
slope sites. Very few explosions were recorded at any of the three
sites throughout the monitoring period. Origin of the few explosions
detected are unknown, but there was no Navy explosive use in the GOA
TMAA during this period, so these explosive-like events may be related
to fisheries activity, lightning strikes, or some other unidentified
source. There were no detections of Navy mid-frequency sonar use in the
recordings (Debich et al. 2013, 2014; U.S. Department of the Navy
2013f, 2014d). In September 2012, an additional HARP buoy was deployed
at Pratt Seamount (near the east end of the GOA TMAA) and in June 2013
two additional buoys were deployed in the GOA TMAA: One at the shelf-
break near the southwest corner of the GOA TMAA and one at Quinn
Seamount (the approximate middle of the GOA TMAA's southeast boundary).
This constitutes a total of five Navy-funded concurrent long-term
passive acoustic monitoring packages present in the GOA TMAA through
fall of 2014. Debich et al. (2013) reported the first detection of a
North Pacific right whale at the Quinn Seamount site. Over two days
between June and August 2013, the Quinn seamount HARP detected three
hours of North Pacific right whale calls (Debich et al., 2014,
[Scaron]irovi[cacute] et al., in press). Given the recording device
location near the southwest border of the GOA TMAA, inability of the
device as configured to determine call directionality, and likely
signal propagation of several 10s of miles, it remains uncertain if the
detected calls orginated within or outside of the GOA TMAA. Previous
related Navy funded monitoring at multiple sites within the Study Area
reported no North Pacific right whale detections (Baumann-Pickering et
al., 2012b, Debich et al., 2013). Additional monitoring conducted in
the GOA TMAA through spring 2015 included the deployment of five HARPs
to detect marine mammals and anthropogenic sounds (Rice et al., 2015).
Future monitoring will include varying numbers of HARPs or other
passive acoustic technologies based on annual Adaptive Management
discussions with NMFS (see U.S. Department of the Navy [2014d] for
details in that regard).
In the Gulf of Alaska, the Navy has also funded two previous marine
mammal surveys to gather occurrence and density data. Although there
was no regulatory requirement for the Navy to undertake either survey,
the Navy funded the data collection to first support analysis of
potential effects for the 2011 GOA FEIS/OEIS and again recently to
support the current SEIS/OEIS. The first Navy-funded survey (GOALS) was
conducted by NMFS in April 2009 (see Rone et al., 2009). Line-transect
survey visual data was gathered to support distance sampling statistics
and acoustic data were collected over a 10-day period both within and
outside the GOA TMAA. This survey resulted in sightings of several
species and allowed for the derivation of densities for fin and
humpback whale that supplemented multiple previous survey efforts in
the
[[Page 9989]]
vicinity (Rone et al., 2009). In summer 2013, the Navy funded an
additional visual line-transect survey in the offshore waters of the
Gulf of Alaska (Rone et al., 2014). The GOALS II survey was a 30-day
visual line-transect survey supplemented by use of passive acoustics
and was a follow-on effort to the previously Navy-funded GOALS survey
in 2009. The primary objectives for the GOALS II survey were to acquire
baseline data to increase understanding of the likely occurrence (i.e.,
presence, abundance, distribution and/or density of species) of beaked
whales and ESA-listed marine mammals in the Gulf of Alaska. Specific
research objectives were:
Assess the abundance, spatial distribution and/or density
of marine mammals, with a focus on beaked whales and ESA-listed
cetacean species through visual line-transect surveys and passive
acoustics using a towed hydrophone array and sonobuoys
Increase knowledge of species' vocal repertoire by linking
visual sightings to vocally active cetaceans, in order to improve the
effectiveness of passive acoustic monitoring
Attempt to photo-identify and biopsy sample individual
whales opportunistically for analysis of population structure, genetics
and habitat use
Attempt to locate whales for opportunistic satellite
tagging using visual and passive acoustic methodology in order to
provide information on both large- and fine-scale movements and habitat
use of cetaceans
The Navy-funded GOALS II survey also sampled four distinct habitat
areas (shelf, slope, offshore, and seamounts) which were partitioned
into four strata. The survey design was intended to provide uniform
coverage within the Gulf of Alaska. However, given the overall limited
knowledge of beaked whales within the Gulf of Alaska, the survey was
also designed to provide coverage of potential beaked whale habitat and
resulted in 13 encounters with beaked whales numbering 67 individual
animals (Rone et al., 2014). The following additional details are
summarized from the presentation in Rone et al. (2014). The visual
survey consisted of 4,504 km (2,431 nm) of `full-effort' and included
349 km (188 nm) of `transit-effort.' There was an additional 375 km
(202 nm) of `fog-effort' (transect and transit). Based on total effort,
there were 802 sightings (1,998 individuals) identified to species,
with an additional 162 sightings (228 individuals) of unidentified
cetaceans and pinnipeds. Acoustic surveying was conducted round-the-
clock with a towed-hydrophone array for 6,304 km (3,997 nm) of line-
transect effort totaling 426 hours of `standard' monitoring, with an
additional 374 km (202 nm) of ~30 hours of `non-standard' and `chase'
effort. There were 379 acoustic detections and 267 localizations of 6
identified cetacean species. Additionally, 186 acoustic sonobuoys were
deployed with 7 identified cetacean species detected. Two satellite
transmitter tags were deployed; a tag on a blue whale (B. musculus)
transmitted for 9 days and a tag on a Baird's beaked whale (Berardius
bairdii) transmitted for 15 days. Based on photo-identification
matches, the tagged blue whale had been previously identified off Baja
California, Mexico, in 2005. Photographs of five cetacean species were
collected for photo-identification purposes: fin, humpback, blue,
killer (Orcinus orca) and Baird's beaked whales. The estimates of
abundance and density for five species were obtained for the first time
for the central Gulf of Alaska. Overall, the Navy funded GOALS II
survey provided one of the most comprehensive datasets on marine mammal
occurrence, abundance, and distribution within that rarely surveyed
area (Rone et al., 2014).
NMFS has acknowledged that the Navy's GOA TMAA monitoring will
enhance understanding of marine mammal vocalizations and distributions
within the offshore waters of the Gulf of Alaska. Additionally, NMFS
pointed out that information gained from the investigations associated
with the Navy's monitoring may be used in the adaptive management of
monitoring measures in subsequent NMFS authorizations, if appropriate
and in consultation with NMFS. The Navy is committed to structuring the
Navy-sponsored research and monitoring program to address both NMFS'
regulatory requirements as part of any MMPA authorizations while at the
same time making significant contributions to the greater body of
marine mammal science (see U.S. Department of the Navy, 2013f).
Pacific Northwest Cetacean Tagging--A Navy-funded effort in the
Pacific Northwest is ongoing and involves attaching long-term satellite
tracking tags to migrating gray whales off the coast of Oregon and
northern California (U.S. Department of the Navy, 2013e). This study is
being conducted by the University of Oregon and has also included
tagging of other large whale species such as humpback whales, fin
whales, and killer whales when encountered. This effort is not
programmed, affiliated, or managed as part of the GOA TMAA monitoring,
and is a separate regional project, but has provided information on
marine mammals and their movements that has application to the Gulf of
Alaska.
In one effort between May 2010 and May 2013, satellite tracking
tags were placed on three gray whales, 11 fin whales, five humpback
whales, and two killer whales off the Washington coast (Schorr et al.,
2013). One tag on an Eastern North Pacific Offshore stock killer whale,
in a pod encountered off Washington at Grays Harbor Canyon, remained
attached and continued to transmit for approximately 3 months. In this
period, the animal transited a distance of approximately 4,700 nm,
which included time spent in the nearshore margins of the TMAA in the
Gulf of Alaska where it would be considered part of the Offshore stock
(for stock designations, see Muto and Angliss, 2015). In a second
effort between 2012 and 2013, tags were attached to 11 Pacific Coast
Feeding Group gray whales near Crescent City, California; in general,
the tag-reported positions indicated these whales were moving southward
at this time of year (Mate, 2013). The Navy's 2013 annual monitoring
report for the Northwest Training and Testing Range contains the
details of the findings from both research efforts described above
(U.S. Department of the Navy, 2013e).
Proposed Monitoring for the GOA TMAA Study Area
Based on NMFS-Navy meetings in June and October 2011, and the
upcoming annual monitoring meeting scheduled for March 2016, future
Navy compliance monitoring, including ongoing monitoring, will address
ICMP top-level goals through a series of regional and ocean basin study
questions with a prioritization and funding focus on species of
interest as identified for each range complex. The ICMP will also
address relative investments to different range complexes based on
goals across all range complexes, and monitoring will leverage multiple
techniques for data acquisition and analysis whenever possible.
Within the GOA TMAA Study Area, the Navy's monitoring for GOA TMAA
under this LOA authorization and concurrently in other areas of the
Pacific Ocean will therefore be structured to address region-specific
species-specific study questions in consultation with NMFS.
The outcome of the March 2016 Navy-NMFS monitoring meeting,
including any proposed monitoring during the period covered by this
proposed rule
[[Page 9990]]
(2016-2021) will be discussed in the final rule. In addition, Navy
monitoring projects proposed during the 2016-2021 GOA TMAA rulemaking
period will be posted on the Navy's marine species monitoring Web site
(https://www.navymarinespeciesmonitoring.us/regions/pacific/current-
projects/).
Ongoing Navy Research
The U.S. Navy is one of the world's leading organizations in
assessing the effects of human activities on the marine environment
including marine mammals. From 2004 through 2013, the Navy has funded
over $240M specifically for marine mammal research. Navy scientists
work cooperatively with other government researchers and scientists,
universities, industry, and non-governmental conservation organizations
in collecting, evaluating, and modeling information on marine
resources. They also develop approaches to ensure that these resources
are minimally impacted by existing and future Navy operations. It is
imperative that the Navy's R&D efforts related to marine mammals are
conducted in an open, transparent manner with validated study needs and
requirements. The goal of the Navy's R&D program is to enable
collection and publication of scientifically valid research as well as
development of techniques and tools for Navy, academic, and commercial
use. Historically, R&D programs are funded and developed by the Navy's
Chief of Naval Operations Energy and Environmental Readiness Division
(OPNAV N45) and Office of Naval Research (ONR), Code 322 Marine Mammals
and Biological Oceanography Program. The primary focus of these
programs since the 1990s is on understanding the effects of sound on
marine mammals, including physiological, behavioral, and ecological
effects.
ONR's current Marine Mammals and Biology Program thrusts include,
but are not limited to: (1) monitoring and detection research, (2)
integrated ecosystem research including sensor and tag development, (3)
effects of sound on marine life (such as hearing, behavioral response
studies, physiology [diving and stress], and PCAD), and (4) models and
databases for environmental compliance.
To manage some of the Navy's marine mammal research programmatic
elements, OPNAV N45 developed in 2011 a new Living Marine Resources
(LMR) Research and Development Program (https://www.lmr.navy.mil/). The
goal of the LMR Research and Development Program is to identify and
fill knowledge gaps and to demonstrate, validate, and integrate new
processes and technologies to minimize potential effects to marine
mammals and other marine resources. Key elements of the LMR program
include:
Providing science-based information to support Navy
environmental effects assessments for research, development,
acquisition, testing and evaluation as well as Fleet at-sea training,
exercises, maintenance and support activities.
Improving knowledge of the status and trends of marine
species of concern and the ecosystems of which they are a part.
Developing the scientific basis for the criteria and
thresholds to measure the effects of Navy generated sound.
Improving understanding of underwater sound and sound
field characterization unique to assessing the biological consequences
resulting from underwater sound (as opposed to tactical applications of
underwater sound or propagation loss modeling for military
communications or tactical applications).
Developing technologies and methods to monitor and, where
possible, mitigate biologically significant consequences to living
marine resources resulting from naval activities, emphasizing those
consequences that are most likely to be biologically significant.
Navy Research and Development
Navy Funded--Both the LMR and ONR Research and Development Programs
periodically fund projects within the Study Area. Some data and
results, when available from these R&D projects, are typically
summarized in the Navy's annual range complex Monitoring Reports that
are currently submitted to the NMFS each year. In addition, the Navy's
Range Complex monitoring during training and testing activities is
coordinated with the R&D monitoring in a given region to leverage
research objectives, assets, and studies where possible under the ICMP.
The integration between the Navy's new LMR Research and Development
Program and related range complex monitoring will continue and improve
during this LOA application period with applicable results presented in
GOA TMAA annual monitoring reports.
Other National Department of Defense Funded Initiatives--Strategic
Environmental Research and Development Program (SERDP) and
Environmental Security Technology Certification Program (ESTCP) are the
DoD's environmental research programs, harnessing the latest science
and technology to improve environmental performance, reduce costs, and
enhance and sustain mission capabilities. The Programs respond to
environmental technology requirements that are common to all of the
military Services, complementing the Services' research programs. SERDP
and ESTCP promote partnerships and collaboration among academia,
industry, the military Services, and other Federal agencies. They are
independent programs managed from a joint office to coordinate the full
spectrum of efforts, from basic and applied research to field
demonstration and validation.
Adaptive Management
The final regulations governing the take of marine mammals
incidental to Navy training activities in the Study Area would contain
an adaptive management component carried over from previous
authorizations. Although better than 5 years ago, our understanding of
the effects of Navy training and testing activities (e.g., MFAS/HFAS,
underwater detonations) on marine mammals is still relatively limited,
and yet the science in this field is evolving fairly quickly. These
circumstances make the inclusion of an adaptive management component
both valuable and necessary within the context of 5-year regulations
for activities that have been associated with marine mammal mortality
in certain circumstances and locations.
The reporting requirements associated with this proposed rule are
designed to provide NMFS with monitoring data from the previous year to
allow NMFS to consider whether any changes are appropriate. NMFS and
the Navy would meet to discuss the monitoring reports, Navy R&D
developments, and current science and whether mitigation or monitoring
modifications are appropriate. The use of adaptive management allows
NMFS to consider new information from different sources to determine
(with input from the Navy regarding practicability) on an annual or
biennial basis if mitigation or monitoring measures should be modified
(including additions or deletions). Mitigation measures could be
modified if new data suggests that such modifications would have a
reasonable likelihood of reducing adverse effects to marine mammals and
if the measures are practicable.
The following are some of the possible sources of applicable data
to be considered through the adaptive management process: (1) Results
from monitoring and exercises reports, as required by MMPA
authorizations; (2) compiled results of Navy funded R&D
[[Page 9991]]
studies; (3) results from specific stranding investigations; (4)
results from general marine mammal and sound research; and (5) any
information which reveals that marine mammals may have been taken in a
manner, extent, or number not authorized by these regulations or
subsequent LOA.
Proposed Reporting
In order to issue an ITA for an activity, section 101(a)(5)(A) of
the MMPA states that NMFS must set forth ``requirements pertaining to
the monitoring and reporting of such taking''. Effective reporting is
critical both to compliance as well as ensuring that the most value is
obtained from the required monitoring. Some of the reporting
requirements are still in development and the final rulemaking may
contain additional details not contained here. Additionally, proposed
reporting requirements may be modified, removed, or added based on
information or comments received during the public comment period.
Reports from individual monitoring events, results of analyses,
publications, and periodic progress reports for specific monitoring
projects would be posted to the Navy's Marine Species Monitoring web
portal: https://www.navymarinespeciesmonitoring.us. Currently, there are
several different reporting requirements pursuant to these proposed
regulations:
General Notification of Injured or Dead Marine Mammals
Navy personnel would ensure that NMFS (the appropriate Regional
Stranding Coordinator) is notified immediately (or as soon as clearance
procedures allow) if an injured or dead marine mammal is found during
or shortly after, and in the vicinity of, any Navy training exercise
utilizing MFAS, HFAS, or underwater explosive detonations. The Navy
would provide NMFS with species identification or a description of the
animal(s), the condition of the animal(s) (including carcass condition
if the animal is dead), location, time of first discovery, observed
behaviors (if alive), and photographs or video (if available). The Navy
shall consult the Stranding Response Plan to obtain more specific
reporting requirements for specific circumstances.
Vessel Strike
NMFS has developed the following language to address monitoring and
reporting measures specific to vessel strike. Most of this language
comes directly from the Stranding Response Plan for other Navy training
and testing rulemakings. This section has also been included in the
regulatory text at the end of this proposed rule. Vessel strike during
Navy training activities in the Study Area is not anticipated; however,
in the event that a Navy vessel strikes a whale, the Navy shall do the
following:
Immediately report to NMFS (pursuant to the established
Communication Protocol) the:
Species identification (if known);
Location (latitude/longitude) of the animal (or location
of the strike if the animal has disappeared);
Whether the animal is alive or dead (or unknown); and
The time of the strike.
As soon as feasible, the Navy shall report to or provide to NMFS,
the:
Size, length, and description (critical if species is not
known) of animal;
An estimate of the injury status (e.g., dead, injured but
alive, injured and moving, blood or tissue observed in the water,
status unknown, disappeared, etc.);
Description of the behavior of the whale during event,
immediately after the strike, and following the strike (until the
report is made or the animal is no longer sighted);
Vessel class/type and operational status;
Vessel length;
Vessel speed and heading; and
To the best extent possible, obtain a photo or video of
the struck animal, if the animal is still in view.
Within 2 weeks of the strike, provide NMFS:
A detailed description of the specific actions of the
vessel in the 30-minute timeframe immediately preceding the strike,
during the event, and immediately after the strike (e.g., the speed and
changes in speed, the direction and changes in direction, other
maneuvers, sonar use, etc., if not classified);
A narrative description of marine mammal sightings during
the event and immediately after, and any information as to sightings
prior to the strike, if available; and use established Navy shipboard
procedures to make a camera available to attempt to capture photographs
following a ship strike.
NMFS and the Navy will coordinate to determine the services the
Navy may provide to assist NMFS with the investigation of the strike.
The response and support activities to be provided by the Navy are
dependent on resource availability, must be consistent with military
security, and must be logistically feasible without compromising Navy
personnel safety. Assistance requested and provided may vary based on
distance of strike from shore, the nature of the vessel that hit the
whale, available nearby Navy resources, operational and installation
commitments, or other factors.
Annual GOA TMAA Monitoring Report
The Navy shall submit an annual report of the GOA TMAA monitoring
describing the implementation and results from the previous calendar
year. Data collection methods will be standardized across range
complexes and study areas to allow for comparison in different
geographic locations. Although additional information will be gathered,
Navy Lookouts collecting marine mammal data pursuant to the GOA TMAA
monitoring plan shall, at a minimum, provide the same marine mammal
observation data required in Sec. 218.155. The report shall be
submitted either 90 days after the calendar year, or 90 days after the
conclusion of the monitoring year to be determined by the Adaptive
Management process. The GOA TMAA Monitoring Report may be provided to
NMFS within a larger report that includes the required Monitoring Plan
reports from multiple range complexes and study areas (the multi-Range
Complex Annual Monitoring Report). Such a report would describe
progress of knowledge made with respect to monitoring plan study
questions across all Navy ranges associated with the Integrated
Comprehensive Monitoring Program. Similar study questions shall be
treated together so that progress on each topic shall be summarized
across all Navy ranges. The report need not include analyses and
content that does not provide direct assessment of cumulative progress
on the monitoring plan study questions.
Annual GOA TMAA Exercise Report
Each year, the Navy shall submit a preliminary report detailing the
status of authorized sound sources within 21 days after the anniversary
of the date of issuance of the LOA. Each year, the Navy shall submit a
detailed report within 3 months after the anniversary of the date of
issuance of the LOA. The annual report shall contain information on
Major Training Exercises (MTEs), Sinking Exercise (SINKEX) events, and
a summary of all sound sources used (total hours or quantity [per the
LOA] of each bin of sonar or other non-impulsive source; total annual
number of each type of explosive exercises; and total annual expended/
detonated rounds [missiles, bombs, sonobuoys, etc.] for each explosive
bin). The analysis in the detailed report will be
[[Page 9992]]
based on the accumulation of data from the current year's report and
data collected from previous the report. Information included in the
classified annual reports may be used to inform future adaptive
management of activities within the GOA TMAA.
Sonar Exercise Notification
The Navy shall submit to NMFS (specific contact information to be
provided in LOA) an electronic report within fifteen calendar days
after the completion of any major training exercise indicating:
Location of the exercise; beginning and end dates of the exercise; and
type of exercise.
5-Year Close-Out Exercise Report
This report will be included as part of the 2021 annual exercise
report. This report will provide the annual totals for each sound
source bin with a comparison to the annual allowance and the 5-year
total for each sound source bin with a comparison to the 5-year
allowance. Additionally, if there were any changes to the sound source
allowance, this report will include a discussion of why the change was
made and include the analysis to support how the change did or did not
result in a change in the SEIS and final rule determinations. The
report will be submitted 3 months after the expiration of the rule.
NMFS will submit comments on the draft close-out report, if any, within
3 months of receipt. The report will be considered final after the Navy
has addressed NMFS' comments, or 3 months after the submittal of the
draft if NMFS does not provide comments.
Estimated Take of Marine Mammals
In the Potential Effects section, NMFS' analysis identified the
lethal responses, physical trauma, sensory impairment (PTS, TTS, and
acoustic masking), physiological responses (particular stress
responses), and behavioral responses that could potentially result from
exposure to MFAS/HFAS or underwater explosive detonations. In this
section, the potential effects to marine mammals from MFAS/HFAS and
underwater detonation of explosives will be related to the MMPA
regulatory definitions of Level A and Level B harassment and we will
attempt to quantify the effects that might occur from the proposed
training activities in the Study Area.
As mentioned previously, behavioral responses are context-
dependent, complex, and influenced to varying degrees by a number of
factors other than just received level. For example, an animal may
respond differently to a sound emanating from a ship that is moving
towards the animal than it would to an identical received level coming
from a vessel that is moving away, or to a ship traveling at a
different speed or at a different distance from the animal. At greater
distances, the nature of vessel movements could also potentially not
have any effect on the animal's response to the sound. In any case, a
full description of the suite of factors that elicited a behavioral
response would require a mention of the vicinity, speed and movement of
the vessel, or other factors. So, while sound sources and the received
levels are the primary focus of the analysis and those that are laid
out quantitatively in the regulatory text, it is with the understanding
that other factors related to the training sometimes contribute to the
behavioral responses of marine mammals, although they cannot be
quantified.
Definition of Harassment
As mentioned previously, with respect to military readiness
activities, section 3(18)(B) of the MMPA defines ``harassment'' as:
``(i) any act that injures or has the significant potential to injure a
marine mammal or marine mammal stock in the wild [Level A Harassment];
or (ii) any act that disturbs or is likely to disturb a marine mammal
or marine mammal stock in the wild by causing disruption of natural
behavioral patterns, including, but not limited to, migration,
surfacing, nursing, breeding, feeding, or sheltering, to a point where
such behavioral patterns are abandoned or significantly altered [Level
B Harassment].'' It is important to note that, as Level B harassment is
interpreted here and quantified by the behavioral thresholds described
below, the fact that a single behavioral pattern (of unspecified
duration) is abandoned or significantly altered and classified as a
Level B take does not mean, necessarily, that the fitness of the
harassed individual is affected either at all or significantly, or
that, for example, a preferred habitat area is abandoned. Further
analysis of context and duration of likely exposures and effects is
necessary to determine the impacts of the estimated effects on
individuals and how those may translate to population level impacts,
and is included in the Analysis and Negligible Impact Determination.
Level B Harassment
Of the potential effects that were described earlier in this
proposed rule, the following are the types of effects that fall into
the Level B harassment category:
Behavioral Harassment--Behavioral disturbance that rises to the
level described in the definition above, when resulting from exposures
to non-impulsive or impulsive sound, is considered Level B harassment.
Some of the lower level physiological stress responses discussed
earlier would also likely co-occur with the predicted harassments,
although these responses are more difficult to detect and fewer data
exist relating these responses to specific received levels of sound.
When Level B harassment is predicted based on estimated behavioral
responses, those takes may have a stress-related physiological
component as well. Except for some vocalization changes that may be
compensating for auditory masking, all behavioral reactions are assumed
to occur due to a preceding stress or cueing response; however, stress
responses cannot be predicted directly due to a lack of scientific
data. Responses can overlap; for example, an increased respiration rate
is likely to be coupled to a flight response or other avoidance
behavior. Factors to consider when trying to predict a stress response
include the mammal's life history stage and whether they are na[iuml]ve
or experienced with the sound. Prior experience with a stressor may be
of particular importance as repeated experience with a stressor may
dull the stress response via acclimation (St. Aubin and Dierauf, 2001;
Bejder et al., 2009).
As the statutory definition is currently applied, a wide range of
behavioral reactions may qualify as Level B harassment under the MMPA,
including but not limited to avoidance of the sound source, temporary
changes in vocalizations or dive patters, temporary avoidance of an
area, or temporary disruption of feeding, migrating, or reproductive
behaviors. The estimates calculated by the Navy using the acoustic
thresholds do not differentiate between the different types of
potential behavioral reactions. Nor do the estimates provide
information regarding the potential fitness or other biological
consequences of the reactions on the affected individuals. We therefore
consider the available scientific evidence to determine the likely
nature of the modeled behavioral responses and the potential fitness
consequences for affected individuals.
Acoustic Masking and Communication Impairment--Acoustic masking and
communication impairment are considered Level B harassment as they can
disrupt natural behavioral patterns by interrupting or limiting the
marine mammal's receipt or transmittal of important information or
[[Page 9993]]
environmental cues. As discussed in the Analysis and Negligible Impact
Determination later in this proposed rule, masking effects from MFAS/
HFAS are expected to be minimal. If masking or communication impairment
were to occur briefly, it would be in the frequency range of MFAS,
which overlaps with some marine mammal vocalizations; however, it would
likely not mask the entirety of any particular vocalization,
communication series, or other critical auditory cue, because the
signal length, frequency, and duty cycle of the MFAS/HFAS signal does
not perfectly mimic the characteristics of any marine mammal's
vocalizations. The other sources used in Navy training, many of either
higher frequencies (meaning that the sounds generated attenuate even
closer to the source) or lower amounts of operation, are similarly not
expected to result in masking or communication impairment.
Temporary Threshold Shift (TTS)--As discussed previously, TTS can
affect how an animal behaves in response to the environment, including
conspecifics, predators, and prey. The following physiological
mechanisms are thought to play a role in inducing auditory fatigue:
Effects to sensory hair cells in the inner ear that reduce their
sensitivity, modification of the chemical environment within the
sensory cells; residual muscular activity in the middle ear,
displacement of certain inner ear membranes; increased blood flow; and
post-stimulatory reduction in both efferent and sensory neural output.
Ward (1997) suggested that when these effects result in TTS rather than
PTS, they are within the normal bounds of physiological variability and
tolerance and do not represent a physical injury. Additionally,
Southall et al. (2007) indicate that although PTS is a tissue injury,
TTS is not because the reduced hearing sensitivity following exposure
to intense sound results primarily from fatigue, not loss, of cochlear
hair cells and supporting structures and is reversible. Accordingly,
NMFS classifies TTS (when resulting from exposure to sonar and other
active acoustic sources and explosives and other impulsive sources) as
Level B harassment, not Level A harassment (injury).
The sound characteristics that correlate with specific stress
responses in marine mammals are poorly understood. Therefore, in
practice, a stress response is assumed if a physiological reaction such
as a hearing loss (threshold shift--i.e., TTS or PTS) or trauma is
predicted (or if a behavioral response is predicted, as discussed in
the Level B Harassment section).
Only non-TTS behavioral reactions and TTS are anticipated with the
GOA TMAA training activities, and these Level B behavioral harassment
takes are enumerated in Tables 12 and 13 and in the Negligible Impact
Determination later in this proposed rule.
Level A Harassment
Of the potential effects that were described earlier, following are
the types of effects that can fall into the Level A harassment category
(unless they further rise to the level of serious injury or mortality):
Permanent Threshold Shift (PTS)--PTS (resulting either from
exposure to MFAS/HFAS or explosive detonations) is irreversible and
considered an injury. PTS results from exposure to intense sounds that
cause a permanent loss of inner or outer cochlear hair cells or exceed
the elastic limits of certain tissues and membranes in the middle and
inner ears and result in changes in the chemical composition of the
inner ear fluids. As mentioned above for TTS, a stress response is
assumed if a physiological reaction such as a hearing loss (PTS) or
trauma is predicted.
As discussed in the Negligible Impact Determination later in this
proposed rule, only a small number (5) of Level A takes resulting from
mild levels of PTS are predicted, and no serious injury or mortality
takes are predicted, with the Navy's training activities in the GOA
TMAA.
Tissue Damage due to Acoustically Mediated Bubble Growth--A few
theories suggest ways in which gas bubbles become enlarged through
exposure to intense sounds (MFAS/HFAS) to the point where tissue damage
results. In rectified diffusion, exposure to a sound field would cause
bubbles to increase in size which could cause tissue damage that would
be considered injurious. A short duration of sonar pings (such as that
which an animal exposed to MFAS would be most likely to encounter)
would not likely be long enough to drive bubble growth to any
substantial size. Alternately, bubbles could be destabilized by high-
level sound exposures such that bubble growth then occurs through
static diffusion of gas out of the tissues. The degree of
supersaturation and exposure levels observed to cause microbubble
destabilization are unlikely to occur, either alone or in concert
because of how close an animal would need to be to the sound source to
be exposed to high enough levels, especially considering the likely
avoidance of the sound source and the required mitigation. For the
reasons above, Level A harassment in the form of tissue damage from
acoustically mediated bubble growth is not predicted for training
activities in the GOA TMAA.
Tissue Damage due to Behaviorally Mediated Bubble Growth--Several
authors suggest mechanisms in which marine mammals could behaviorally
respond to exposure to MFAS/HFAS by altering their dive patterns
(unusually rapid ascent, unusually long series of surface dives, etc.)
in a manner that might result in unusual bubble formation or growth
ultimately resulting in tissue damage. In this scenario, the rate of
ascent would need to be sufficiently rapid to compromise behavioral or
physiological protections against nitrogen bubble formation.
There is considerable disagreement among scientists as to the
likelihood of this phenomenon (Piantadosi and Thalmann, 2004; Evans and
Miller, 2003). Although it has been argued that traumas from recent
beaked whale strandings are consistent with gas emboli and bubble-
induced tissue separations (Jepson et al., 2003; Fernandez et al.,
2005; Fern[aacute]ndez et al., 2012), nitrogen bubble formation as the
cause of the traumas has not been verified. If tissue damage does occur
by this phenomenon, it would be considered an injury. Recent modeling
by Kvadsheim et al. (2012) determined that while behavioral and
physiological responses to sonar have the potential to result in bubble
formation, the actual observed behavioral responses of cetaceans to
sonar did not imply any significantly increased risk over what may
otherwise occur normally in individual marine mammals. Level A
harassment in the form of tissue damage from behaviorally mediated
bubble growth is not anticipated for training activities in the GOA
TMAA.
Physical Disruption of Tissues Resulting from Explosive Shock
Wave--Physical damage of tissues resulting from a shock wave (from an
explosive detonation) is classified as an injury. Blast effects are
greatest at the gas-liquid interface (Landsberg, 2000) and gas-
containing organs, particularly the lungs and gastrointestinal tract,
are especially susceptible (Goertner, 1982; Hill 1978; Yelverton et
al., 1973). Nasal sacs, larynx, pharynx, trachea, and lungs may be
damaged by compression/expansion caused by the oscillations of the
blast gas bubble (Reidenberg and Laitman, 2003). Severe damage (from
the shock wave) to the ears can include tympanic membrane rupture,
fracture of the ossicles, damage to the cochlea, hemorrhage, and
cerebrospinal fluid leakage into the middle ear. Explosions in the
ocean or near the water surface can introduce loud, impulsive,
[[Page 9994]]
broadband sounds into the marine environment. These sounds are likely
within the audible range of most marine mammals, but the duration of
individual sounds is very short. The direct sound from explosions used
during training activities last less than a second, and most events
involve the use of only one or a few explosions. Furthermore, events
are dispersed in time and throughout the GOA TMAA Study Area. These
factors reduce the likelihood of these sources causing substantial
physical disruption of tissues in marine mammals, especially when the
avoidance and mitigation factors are taken into consideration.
Consequently, no Level A harassment from explosive shock waves is
anticipated from training activities in the GOA TMAA.
Vessel or Ordnance Strike--Vessel strike or ordnance strike
associated with the specified activities would be considered Level A
harassment, serious injury, or mortality. There are no records of any
Navy vessel strikes to marine mammals during training activities in the
GOA TMMA Study Area. There have been Navy strikes of large whales in
areas outside the Study Area, such as Hawaii and Southern California.
However, these areas differ significantly from the Study Area given
that both Hawaii and Southern California have a much higher number of
Navy vessel activities and much higher densities of large whales. The
Navy's proposed actions would not result in any appreciable changes in
locations or frequency of vessel activity, and there have been no whale
strikes during any previous training activities in the Study Area. The
manner in which the Navy has trained would remain consistent with the
range of variability observed over the last decade so the Navy does not
anticipate vessel strikes would occur within the Study Area during
training events. As such, vessel or ordnance strike is not anticipated
with the Navy activities in the Study Area and Level A harassment,
serious injury, or mortality are not expected.
Take Thresholds
For the purposes of an MMPA authorization, three types of take are
identified: Level B harassment; Level A harassment; and mortality (or
serious injury leading to mortality). The categories of marine mammal
responses (physiological and behavioral) that fall into the two
harassment categories were described in the previous section.
Because the physiological and behavioral responses of the majority
of the marine mammals exposed to non-impulse and impulse sounds cannot
be easily detected or measured, and because NMFS must authorize take
prior to the impacts to marine mammals, a method is needed to estimate
the number of individuals that will be taken, pursuant to the MMPA,
based on the proposed action. To this end, NMFS developed acoustic
thresholds that estimate at what received level (when exposed to non-
impulse or impulse sounds) Level B harassment and Level A harassment of
marine mammals would occur. The acoustic thresholds for non-impulse and
impulse sounds are discussed below.
Level B Harassment Threshold (TTS)--Behavioral disturbance,
acoustic masking, and TTS are all considered Level B harassment. Marine
mammals would usually be behaviorally disturbed at lower received
levels than those at which they would likely sustain TTS, so the levels
at which behavioral disturbance are likely to occur is considered the
onset of Level B harassment. The behavioral responses of marine mammals
to sound are variable, context specific, and, therefore, difficult to
quantify (see Risk Function section, below).
TTS is a physiological effect that has been studied and quantified
in laboratory conditions. Because data exist to support an estimate of
the received levels at which marine mammals will incur TTS, NMFS uses
an acoustic criteria to estimate the number of marine mammals that
might sustain TTS. TTS is a subset of Level B harassment (along with
sub-TTS behavioral harassment) and the Navy is not specifically
required to estimate those numbers; however, the more specifically the
affected marine mammal responses can be estimated, the better the
analysis.
Level A Harassment Threshold (PTS)--For acoustic effects, because
the tissues of the ear appear to be the most susceptible to the
physiological effects of sound, and because threshold shifts tend to
occur at lower exposures than other more serious auditory effects, NMFS
has determined that PTS is the best indicator for the smallest degree
of injury that can be measured. Therefore, the acoustic exposure
associated with onset-PTS is used to define the lower limit of Level A
harassment.
PTS data do not currently exist for marine mammals and are unlikely
to be obtained due to ethical concerns. However, PTS levels for these
animals may be estimated using TTS data from marine mammals and
relationships between TTS and PTS that have been determined through
study of terrestrial mammals.
We note here that behaviorally mediated injuries (such as those
that have been hypothesized as the cause of some beaked whale
strandings) could potentially occur in response to received levels
lower than those believed to directly result in tissue damage. As
mentioned previously, data to support a quantitative estimate of these
potential effects (for which the exact mechanism is not known and in
which factors other than received level may play a significant role) do
not exist. However, based on the number of years (more than 60) and
number of hours of MFAS per year that the U.S. (and other countries)
has operated compared to the reported (and verified) cases of
associated marine mammal strandings, NMFS believes that the probability
of these types of injuries is very low. Tables 9 and 10 provide a
summary of non-impulsive and impulsive thresholds to TTS and PTS for
marine mammals. A detailed explanation of how these thresholds were
derived is provided in the Criteria and Thresholds Technical Report
(Finneran and Jenkins, 2012) and summarized in Chapter 6 of the LOA
application (https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm).
Table 9--Onset TTS and PTS Thresholds for Non-Impulse Sound
----------------------------------------------------------------------------------------------------------------
Group Species Onset TTS Onset PTS
----------------------------------------------------------------------------------------------------------------
Low-Frequency Cetaceans.............. All mysticetes......... 178 dB re 1[micro]Pa2- 198 dB re 1[micro]Pa2-
sec(LFII). sec(LFII).
Mid-Frequency Cetaceans.............. Most delphinids, beaked 178 dB re 1[micro]Pa2- 198 dB re 1[micro]Pa2-
whales, medium and sec(MFII). sec(MFII).
large toothed whales.
High-Frequency Cetaceans............. Porpoises, Kogia spp... 152 dB re 1[micro]Pa2- 172 dB re 1[micro]Pa2-
sec(HFII). secSEL (HFII).
Phocidae In-water.................... Harbor, Hawaiian monk, 183 dB re 1[micro]Pa2- 197 dB re 1[micro]Pa2-
elephant seals. sec(PWI). sec(PWI).
[[Page 9995]]
Otariidae & Obodenidae In-water...... Sea lions and fur seals 206 dB re 1[micro]Pa2- 220 dB re 1[micro]Pa2-
sec(OWI). sec(OWI).
Mustelidae In-water.................. Sea otters.............
----------------------------------------------------------------------------------------------------------------
LFII, MFII, HFII: New compound Type II weighting functions; PWI, OWI: Original Type I (Southall et al., 2007)
for pinniped and mustelid in water.
[GRAPHIC] [TIFF OMITTED] TP26FE16.000
Level B Harassment Risk Function (Behavioral Harassment)
As the statutory definition is currently applied, a wide range of
behavioral reactions may qualify as Level B harassment under the MMPA,
including but not limited to avoidance of the sound source, temporary
changes in vocalizations or dive patters, temporary avoidance of an
area, or temporary disruption of feeding, migrating, or reproductive
behaviors. The estimates
[[Page 9996]]
calculated by the Navy using the acoustic thresholds do not
differentiate between the different types of potential behavioral
reactions. Nor do the estimates provide information regarding the
potential fitness or other biological consequences of the reactions on
the affected individuals. We therefore consider the available
scientific evidence to determine the likely nature of the modeled
behavioral responses and the potential fitness consequences for
affected individuals.
Behavioral Response Criteria for Non-Impulsive Sound from Sonar and
other Active Sources--In 2006, NMFS issued the first MMPA authorization
to allow the take of marine mammals incidental to MFAS (to the Navy for
RIMPAC). For that authorization, NMFS used 173 dB SEL as the criterion
for the onset of behavioral harassment (Level B harassment). This type
of single number criterion is referred to as a step function, in which
(in this example) all animals estimated to be exposed to received
levels above 173 db SEL would be predicted to be taken by Level B
Harassment and all animals exposed to less than 173 dB SEL would not be
taken by Level B harassment. As mentioned previously, marine mammal
behavioral responses to sound are highly variable and context specific
(affected by differences in acoustic conditions; differences between
species and populations; differences in gender, age, reproductive
status, or social behavior; or the prior experience of the
individuals), which means that there is support for alternate
approaches for estimating behavioral harassment.
Unlike step functions, acoustic risk continuum functions (which are
also called ``exposure-response functions'' or ``dose-response
functions'' in other risk assessment contexts) allow for probability of
a response that NMFS would classify as harassment to occur over a range
of possible received levels (instead of one number) and assume that the
probability of a response depends first on the ``dose'' (in this case,
the received level of sound) and that the probability of a response
increases as the ``dose'' increases. In January 2009, NMFS issued three
final rules governing the incidental take of marine mammals (within
Navy's Hawaii Range, Southern California Training and Testing Range,
and Atlantic Fleet Active Sonar Training complexes) that used a risk
continuum to estimate the percent of marine mammals exposed to various
levels of MFAS that would respond in a manner NMFS considers
harassment.
The Navy and NMFS have previously used acoustic risk functions to
estimate the probable responses of marine mammals to acoustic exposures
for other training and research programs. Examples of previous
application include the Navy FEISs on the Surveillance Towed Array
Sensor System Low Frequency Active (SURTASS LFA) sonar (U.S. Department
of the Navy, 2001c); the North Pacific Acoustic Laboratory experiments
conducted off the Island of Kauai (Office of Naval Research, 2001), and
the Supplemental EIS for SURTASS LFA sonar (U.S. Department of the
Navy, 2007d). As discussed earlier, factors other than received level
(such as distance from or bearing to the sound source, context of
animal at time of exposure) can affect the way that marine mammals
respond; however, data to support a quantitative analysis of those (and
other factors) do not currently exist. It is also worth specifically
noting that while context is very important in marine mammal response,
given otherwise equivalent context, the severity of a marine mammal
behavioral response is also expected to increase with received level
(Houser and Moore, 2014). NMFS will continue to modify these criteria
as new data become available and can be appropriately and effectively
incorporated.
The particular acoustic risk functions developed by NMFS and the
Navy (see Figures 1 and 2 of the LOA application) estimate the
probability of behavioral responses to MFAS/HFAS (interpreted as the
percentage of the exposed population) that NMFS would classify as
harassment for the purposes of the MMPA given exposure to specific
received levels of MFAS/HFAS. The mathematical function (below)
underlying this curve is a cumulative probability distribution adapted
from a solution in Feller (1968) and was also used in predicting risk
for the Navy's SURTASS LFA MMPA authorization as well.
[GRAPHIC] [TIFF OMITTED] TP26FE16.001
Where:
R = Risk (0--1.0)
L = Received level (dB re: 1 [micro]Pa)
B = Basement received level = 120 dB re: 1 [micro]Pa
K = Received level increment above B where 50-percent risk = 45 dB
re: 1 [micro]Pa
A = Risk transition sharpness parameter = 10 (odontocetes and
pinnipeds) or 8 (mysticetes)
Detailed information on the above equation and its parameters is
available in the LOA application and previous Navy documents listed
above.
The harbor porpoise and beaked whales have unique criteria based on
specific data that show these animals to be especially sensitive to
sound. Harbor porpoise and beaked whale non-impulsive behavioral
criteria are used unweighted--without weighting the received level
before comparing it to the threshold (see Finneran and Jenkins, 2012).
It has been speculated for some time that beaked whales might have
unusual sensitivities to sonar sound due to their likelihood of
stranding in conjunction with mid-frequency sonar use, even in areas
where other species were more abundant (D'Amico et al., 2009), but
there were not sufficient data to support a separate treatment for
beaked whales until recently. With the recent publication of results
from Blainville's beaked whale monitoring and experimental exposure
studies on the instrumented AUTEC range in the Bahamas (McCarthy et al.
2011; Tyack et al. 2011), there are now statistically strong data
suggesting that beaked whales tend to avoid actual naval mid-frequency
sonar in real anti-submarine training scenarios as well as playbacks of
killer whale vocalizations, and other anthropogenic sounds. Tyack et
al. (2011) report that, in reaction to sonar playbacks, most beaked
whales stopped echolocating, made long slow ascent, and moved away from
the sound. During an exercise using mid-frequency sonar, beaked whales
avoided the sonar acoustic footprint at a distance where the received
level was ``around 140 dB'' (SPL) and once the exercise ended, beaked
whales re-inhabited the center of exercise area within 2-3 days (Tyack
et al., 2011). The Navy has therefore adopted an unweighted 140 dB re 1
[micro]Pa SPL threshold for significant behavioral effects for all
beaked whales (family: Ziphiidae).
Since the development of the criterion, analysis of the data the
2010 and 2011 field seasons of the southern California Behavioral
Responses Study have been published. The study, DeRuiter et al.
(2013b), provides similar evidence of Cuvier's beaked whale
sensitivities to sound based on two controlled exposures. Two whales,
one in each season, were tagged and exposed to simulated mid-frequency
active sonar at distances of 3.4-9.5 km. The 2011 whale was also
incidentally exposed to mid-frequency active sonar from a distant naval
exercise (approximately 118 km away). Received levels from the mid-
frequency active sonar signals during the controlled and incidental
exposures were calculated as
[[Page 9997]]
84-144 and 78-106 dB re 1 [micro]Pa rms, respectively. Both whales
showed responses to the controlled exposures, ranging from initial
orientation changes to avoidance responses characterized by energetic
fluking and swimming away from the source. However, the authors did not
detect similar responses to incidental exposure to distant naval sonar
exercises at comparable received levels, indicating that context of the
exposures (e.g., source proximity, controlled source ramp-up) may have
been a significant factor. Because the sample size was limited
(controlled exposures during a single dive in both 2010 and 2011) and
baseline behavioral data was obtained from different stocks and
geographic areas (i.e., Hawaii and Mediterranean Sea), and the
responses exhibited to controlled exposures were not exhibited by an
animal exposed to some of the same received levels of real sonar
exercises, the Navy relied on the studies at the AUTEC that analyzed
beaked whale responses to actual naval exercises using mid-frequency
active sonar to evaluate potential behavioral responses by beaked
whales to proposed training and testing activities using sonar and
other active acoustic sources.
The information currently available regarding harbor porpoises
suggests a very low threshold level of response for both captive and
wild animals. Threshold levels at which both captive (Kastelein et al.,
2000; Kastelein et al., 2005; Kastelein et al., 2006; Kastelein et al.,
2008) and wild harbor porpoises (Johnston, 2002) responded to sound
(e.g., acoustic harassment devices, acoustic deterrent devices, or
other non-impulsive sound sources) are very low (e.g., approximately
120 dB re 1 [mu]Pa). Therefore, a SPL of 120 dB re 1 [mu]Pa is used in
this analysis as a threshold for predicting behavioral responses in
harbor porpoises instead of the risk functions used for other species
(i.e., we assume for the purpose of estimating take that all harbor
porpoises exposed to 120 dB or higher MFAS/HFAS will be taken by Level
B behavioral harassment).
Behavioral Response Criteria for Impulsive Sound from Explosions --
If more than one explosive event occurs within any given 24-hour period
within a training or testing event, behavioral criteria are applied to
predict the number of animals that may be taken by Level B harassment.
For multiple explosive events the behavioral threshold used in this
analysis is 5 dB less than the TTS onset threshold (in sound exposure
level). This value is derived from observed onsets of behavioral
response by test subjects (bottlenose dolphins) during non-impulse TTS
testing (Schlundt et al., 2000). Some multiple explosive events, such
as certain naval gunnery exercises, may be treated as a single
impulsive event because a few explosions occur closely spaced within a
very short period of time (a few seconds). For single impulses at
received sound levels below hearing loss thresholds, the most likely
behavioral response is a brief alerting or orienting response. Since no
further sounds follow the initial brief impulses, Level B take in the
form of behavioral harassment beyond that associated with potential TTS
would not be expected to occur. This reasoning was applied to previous
shock trials (63 FR 230; 66 FR 87; 73 FR 143) and is extended to these
Phase 2 criteria. Behavioral thresholds for impulsive sources are
summarized in Table 11 and further detailed in the LOA application.
Since impulse events can be quite short, it may be possible to
accumulate multiple received impulses at sound pressure levels
considerably above the energy-based criterion and still not be
considered a behavioral take. The Navy treats all individual received
impulses as if they were one second long for the purposes of
calculating cumulative sound exposure level for multiple impulse
events. For example, five air gun impulses, each 0.1 second long,
received at a Type II weighted sound pressure level of 167 dB SPL would
equal a 164 dB sound exposure level, and would not be predicted as
leading to a significant behavioral response (take) in MF or HF
cetaceans. However, if the five 0.1 second pulses are treated as a 5
second exposure, it would yield an adjusted SEL of approximately 169
dB, exceeding the behavioral threshold of 167 dB SEL. For impulses
associated with explosions that have durations of a few microseconds,
this assumption greatly overestimates effects based on sound exposure
level metrics such as TTS and PTS and behavioral responses. Appropriate
weighting values will be applied to the received impulse in one-third
octave bands and the energy summed to produce a total weighted sound
exposure level value. For impulsive behavioral criteria, the Navy's
weighting functions (detailed in Chapter 6 of the LOA application) are
applied to the received sound level before being compared to the
threshold.
Table 11--Behavioral Thresholds for Impulsive Sound
------------------------------------------------------------------------
Impulsive
behavioral
Hearing group threshold for > 2 Onset TTS
pulses/24 hours
------------------------------------------------------------------------
Low-Frequency Cetaceans......... 167 dB SEL (LFII). 172 dB SEL (MFII)
or 224 dB Peak
SPL.
Mid-Frequency Cetaceans......... 167 dB SEL (MFII).
High-Frequency Cetaceans........ 141 dB SEL (HFII). 146 dB SEL (HFII)
or 195 dB Peak
SPL.
Phocid Seals (in water)......... 172 dB SEL (PWI).. 177 dB SEL (PWI)
or 212 dB Peak
SPL.
Otariidae & Mustelidae (in 195 dB SEL (OWI).. 200 dB SEL (OWI)
water). or 212 dB Peak
SPL.
------------------------------------------------------------------------
Notes: (1) LFII, MFII, HFII are New compound Type II weighting
functions; PWI, OWI = Original Type I (Southall et al., 2007) for
pinniped and mustelid in water (see Finneran and Jenkins 2012). (2)
SEL = re 1 [mu]Pa\2\-s; SPL = re 1 [mu]Pa, SEL = Sound Exposure Level,
dB = decibel, SPL = Sound Pressure Level.
Marine Mammal Density Estimates
A quantitative impact analysis requires an estimate of the number
of animals that might be affected by anthropogenic activities. A key
element of this estimation is knowledge of the abundance and
concentration of the species in specific areas where those activities
will occur. The most appropriate unit of metric for this type of
analysis is animal density, or the number of animals present per unit
area. Marine species density estimation requires a significant amount
of effort to both collect and analyze data to produce a reasonable
estimate. Unlike surveys for terrestrial wildlife, many marine species
spend much of their time submerged, and are not easily observed. In
order to collect enough sighting data to make reasonable density
estimates, multiple observations are required, often in areas that are
not easily accessible (e.g., far offshore). Ideally, marine species
sighting data would be collected for the specific area and time period
(e.g., season) of interest and density estimates derived accordingly.
However, in many places, poor weather conditions and high sea states
prohibit
[[Page 9998]]
the completion of comprehensive visual surveys.
For most cetacean species, abundance is estimated using line-
transect surveys or mark-recapture studies (e.g., Barlow, 2010, Barlow
and Forney, 2007, Calambokidis et al., 2008). The result provides one
single density estimate value for each species across broad geographic
areas, such as waters within the U.S. EEZ off California, Oregon, and
Washington. This is the general approach applied in estimating cetacean
abundance in the NMFS Stock Assessment Reports. Although the single
value provides a good average estimate of abundance (total number of
individuals) for a specified area, it does not provide information on
the species distribution or concentrations within that area, and it
does not estimate density for other timeframes or seasons that were not
surveyed. More recently, habitat modeling has been used to estimate
cetacean densities (Barlow et al., 2009; Becker et al., 2010, 2012a, b,
c; Ferguson et al., 2006a; Forney et al., 2012; Redfern et al., 2006).
These models estimate cetacean density as a continuous function of
habitat variables (e.g., sea surface temperature, seafloor depth, etc.)
and thus allow predictions of cetacean densities on finer spatial
scales than traditional line-transect or mark-recapture analyses.
Within the geographic area that was modeled, densities can be predicted
wherever these habitat variables can be measured or estimated.
Uncertainty in published density estimates is typically large
because of the low number of sightings available for their derivation.
Uncertainty is typically expressed by the coefficient of variation (CV)
of the estimate, which is derived using standard statistical methods
and describes the amount of variation with respect to the population
mean. It is expressed as a fraction or sometimes a percentage and can
range upward from zero, indicating no uncertainty, to high values. For
example, a CV of 0.85 would indicate high uncertainty in the population
estimate. When the CV exceeds 1.0, the estimate is very uncertain. The
uncertainty associated with movements of animals into or out of an area
(due to factors such as availability of prey or changing oceanographic
conditions) is much larger than is indicated by the CV.
The methods used to estimate pinniped at-sea densities are
typically different than those used for cetaceans. This is discussed in
more detail in the Navy Marine Species Density Database Technical
Report (U.S. Department of the Navy, 2014). Pinniped abundance is
generally estimated via shore counts of animals at known rookeries and
haulout sites. Translating these numbers to in-water densities is
difficult given the variability in foraging ranges, migration, and
haulout behavior between species and within each species, and is driven
by factors such as age class, sex class, seasonal variation, etc.
Details of the density derivation for each species of pinniped in the
Study Area are provided in the U.S. Department of the Navy (2014). In
summary, the methods used to derive pinniped densities involved a
series of species-specific data reviews to compile the most accurate
and up-to-date information available. The total abundance divided by
the area of the region was the resultant density estimate for each
species in a given location.
There is no single source of density data for every area, marine
mammal species, and season because of the fiscal costs, resources, and
effort involved to provide enough survey coverage to sufficiently
estimate density. NMFS Southwest Fisheries Science Center conducts
standard U.S. West Coast surveys every 5-6 years and cannot
logistically support more frequent studies. The U.S. Navy has funded
two previous marine mammal surveys in the GOA TMAA (Rone et al., 2009,
2014) in the summer time-period when Navy training activities are most
likely to occur. The density data used to quantitatively estimate
impacts to marine mammals from Navy training in the GOA TMAA are based
on the best available science and were agreed upon with NMFS as a
cooperating agency for the SEIS/OEIS. As the federal regulator for the
MMPA, the NMFS role included having staff biologists review and comment
on the analysis and the SEIS/OEIS. The review also included
coordination with NMFS regional scientists from the Southwest Fisheries
Science Center and Alaska Fisheries Science Center on the latest
emergent data presented in their Pacific Stock Assessment Reports.
In May 2015, the Marine Mammal Commission also reviewed the Marine
Species Density Database Technical Report (U.S. Department of the Navy,
2014) and pointed out some textual errors that the Navy subsequently
corrected, but otherwise did not identify any changes in the data used
for acoustic effects modeling.
A certain number of sightings are required to generate the quality
of data necessary to produce either traditional line-transect density
estimates or spatial habitat modeled density values. The at-sea
identification of some species of specific MMPA designated stocks is
not always possible from available field data, nor would additional
data collection likely address the identification issue based on low
animal occurrence (e.g., Western North Pacific gray whale), cryptic
behaviors (e.g., beaked whales), and appearance similarities between
stocks (e.g., Steller sea lions). In the absence of species-specific
population survey data for these species, density estimates are derived
from different methods and data sources, based on NMFS recommendations.
The different methods for each of these species are described in
Section 3.8.3.1.6.1 (Marine Species Density Data) of the DSEIS/OEIS and
the Marine Species Density Database Technical Report (U.S. Department
of the Navy, 2014). NMFS and Navy have determined that these
alternative density estimates are sufficient for determining the
impacts of Navy training on these marine mammals under all applicable
statutes, and therefore are the best available science.
Therefore, to characterize marine mammal density for areas of
concern, including the GOA TMAA Study Area, the Navy compiled data from
multiple sources. Each data source may use different methods to
estimate density and uncertainty (e.g., variance) associated with the
estimates.
The Navy thus developed a protocol to select the best available
data sources based on species, area, and time (season). The Navy then
used this protocol to identify the best density data from available
sources, including habitat-based density models, line-transect
analyses, and peer-reviewed published studies. These data were
incorporated into a Geographic Information System database that
includes seasonal (summer/fall and winter/spring) density values for
every marine mammal species present within the Study Area. Detailed
information on the Navy's selection protocol, datasets, and specific
density values are provided in the Navy Marine Species Density Database
Technical Report (U.S. Department of the Navy, 2014).
Quantitative Modeling To Estimate Take for Impulsive and Non-Impulsive
Sound
The Navy performed a quantitative analysis to estimate the number
of marine mammals that could be affected by acoustic sources or
explosives used during Navy training activities. Inputs to the
quantitative analysis include marine mammal density estimates; marine
mammal depth occurrence distributions; oceanographic and environmental
data; marine mammal hearing data; and criteria and thresholds for
levels of potential effects. The quantitative analysis consists of
[[Page 9999]]
computer modeled estimates and a post-model analysis to determine the
number of potential mortalities and harassments. The model calculates
sound energy propagation from sonar, other active acoustic sources, and
explosives during naval activities; the sound or impulse received by
animat (virtual representation of an animal) dosimeters representing
marine mammals distributed in the area around the modeled activity; and
whether the sound or impulse received by a marine mammal exceeds the
thresholds for effects. The model estimates are then further analyzed
to consider animal avoidance and implementation of mitigation measures,
resulting in final estimates of potential effects due to Navy training.
Various computer models and mathematical equations can be used to
predict how energy spreads from a sound source (e.g., sonar or
underwater detonation) to a receiver (e.g., dolphin or sea turtle).
Basic underwater sound models calculate the overlap of energy and
marine life using assumptions that account for the many, variable, and
often unknown factors that can influence the result. Assumptions in
previous and current Navy models have intentionally erred on the side
of overestimation when there are unknowns or when the addition of other
variables was not likely to substantively change the final analysis.
For example, because the ocean environment is extremely dynamic and
information is often limited to a synthesis of data gathered over wide
areas and requiring many years of research, known information tends to
be an average of a seasonal or annual variation. El Ni[ntilde]o
Southern Oscillation events of the ocean-atmosphere system are an
example of dynamic change where unusually warm or cold ocean
temperatures are likely to redistribute marine life and alter the
propagation of underwater sound energy. Previous Navy modeling
therefore made some assumptions indicative of a maximum theoretical
propagation for sound energy (such as a perfectly reflective ocean
surface and a flat seafloor).
More complex computer models build upon basic modeling by factoring
in additional variables in an effort to be more accurate by accounting
for such things as variable bathymetry and an animal's likely presence
at various depths.
The Navy has developed new software tools, up to date marine mammal
density data, and other oceanographic data for the quantification of
estimated acoustic impacts to marine mammal impacts from Navy
activities. This new approach is the resulting evolution of the basic
model previously used by the Navy and reflects a more complex modeling
approach as described below. The new model, NAEMO, is the standard
model now used by the navy to estimate the potential acoustic effects
of Navy training and testing activities on marine mammals. Although
this more complex computer modeling approach accounts for various
environmental factors affecting acoustic propagation, the current
software tools do not consider the likelihood that a marine mammal
would attempt to avoid repeated exposures to a sound or avoid an area
of intense activity where a training or testing event may be focused.
Additionally, the software tools do not consider the implementation of
mitigation (e.g., stopping sonar transmissions when a marine mammal is
within a certain distance of a ship or mitigation zone clearance prior
to detonations). In both of these situations, naval activities are
modeled as though an activity would occur regardless of proximity to
marine mammals and without any horizontal movement by the animal away
from the sound source or human activities. Therefore, the final step of
the quantitative analysis of acoustic effects is to consider the
implementation of mitigation and the possibility that marine mammals
would avoid continued or repeated sound exposures. This final, post-
analysis step in the modeling process is meant to better quantify the
predicted effects by accounting for likely animal avoidance behavior
and implementation of standard Navy mitigations.
The incorporation of mitigation factors for the reduction of
predicted effects used a conservative approach (erring on the side of
overestimating the number of effects) since reductions as a result of
implemented mitigation were only applied to those events having a very
high likelihood of detecting marine mammals.
The steps of the quantitative analysis of acoustic effects, the
values and assumptions that went into the Navy's model, and the
resulting ranges to effects are detailed in Chapter 6 (Section 6.5) of
the LOA application (https://www.nmfs.noaa.gov/pr/permits/incidental/).
Details of the model's processes and the description and derivation of
the inputs are presented in the Navy's Determination of Acoustic
Effects technical Report (Marine Species Modeling Team, 2014). The
post-model analysis, which considers the potential for avoidance and
highly effective mitigation during the use of sonar and other active
acoustic sources and explosives, is described in Section 6.5 of the LOA
application. A detailed explanation of the post-model acoustic effect
analysis quantification process is also provided in the technical
report Post-Model Quantitative Analysis of Animal Avoidance Behavior
and Mitigation Effectiveness for the Gulf of Alaska Training (U.S.
Department of the Navy, 2014c; also available at: https://goaeis.com/Documents/SupplementalEISOEISDocumentsandReferences/SupportingTechnicalDocuments.aspx).
Take Request
The GOA DSEIS/OEIS considered all training activities proposed to
occur in the Study Area that have the potential to result in the MMPA
defined take of marine mammals. The stressors associated with these
activities included the following:
Acoustic (sonar and other active non-impulse sources,
explosives, swimmer defense airguns, weapons firing, launch and impact
noise, vessel noise, aircraft noise);
Energy (electromagnetic devices);
Physical disturbance or strikes (vessels, in-water
devices, military expended materials, seafloor devices);
Entanglement (fiber optic cables, guidance wires,
parachutes);
Ingestion (munitions, military expended materials other
than munitions); and
Secondary stressors (sediments and water quality).
The Navy determined, and NMFS agrees, that two stressors could
potentially result in the incidental taking of marine mammals from
training activities within the Study Area: (1) Non-impulsive stressors
(sonar and other active acoustic sources) and (2) impulsive stressors
(explosives). Non-impulsive and impulsive stressors have the potential
to result in incidental takes of marine mammals by harassment, injury,
or mortality.
Training Activities
A detailed analysis of effects due to marine mammal exposures to
impulsive and non-impulsive sources in the Study Area is presented in
Chapter 6 of the LOA application. Based on the model and post-model
analysis described in Chapter 6 of the LOA application, Table 12
summarizes the Navy's final take request for training activities for a
year (up to 2 exercises occurring over a 7-month period [April-
October]) and the summation over a 5-year period (up to 2 exercises
occurring over a 7-month period [April-October] for a total of 10
exercises).
[[Page 10000]]
Table 12--Summary of Annual and 5-Year Take Requests for GOA TMAA Training Activities
----------------------------------------------------------------------------------------------------------------
Training activities
-------------------------------------------------
MMPA Category Source Annual authorization 5-Year authorization
sought sought
----------------------------------------------------------------------------------------------------------------
Mortality............................ Explosives............. 0...................... 0.
Level A.............................. Sonar and other active 5 (Dall's porpoise only 25 (Dall's porpoise
acoustic sources; as shown in Table 13). only as shown in Table
explosives. 13).
Level B.............................. Sonar and other active 36,522 (Species 182,610 (Species
acoustic sources; specific data shown in specific data shown in
explosives. Table 13). Table 13).
----------------------------------------------------------------------------------------------------------------
Impulsive and Non-Impulsive Sources
Table 13 provides details on the Navy's final take request for
training activities by species from the acoustic effects modeling
estimates. Derivations of the numbers presented in Table 13 are
described in more detail within Chapter 6 of the LOA application. Level
A effects are only predicted to occur for Dall's porpoises. There are
no mortalities predicted for any of the proposed training activities.
Table 13--Species-Specific Take Requests From Modeling Estimates of Impulsive and Non-Impulsive Source Effects
for All Training Activities
----------------------------------------------------------------------------------------------------------------
Annual 5-Year
Species Stock ---------------------------------------------------------------
Level B Level A Level B Level A
----------------------------------------------------------------------------------------------------------------
North Pacific right whale..... Eastern North 7 0 35 0
Pacific.
Humpback whale................ Central North 129 0 645 0
Pacific.
Western North 10 0 50 0
Pacific.
Blue whale.................... Eastern North 95 0 475 0
Pacific.
Central North 0 0 0 0
Pacific.
Fin whale..................... Northeast 2,582 0 12,910 0
Pacific.
Sei whale..................... Eastern North 13 0 65 0
Pacific.
Minke whale................... Alaska.......... 87 0 435 0
Gray whale.................... Eastern North 0 0 0 0
Pacific.
Western North 0 0 0 0
Pacific.
Sperm whale................... North Pacific... 197 0 985 0
Killer whale.................. Alaska Resident. 564 0 2,820 0
Eastern North 53 0 265 0
Pacific
Offshore.
AT1 Transient... 1 0 5 0
GOA, Aleutian 144 0 720 0
Island, and
Bearing Sea
Transient.
Pacific white-sided dolphin... North Pacific... 1,963 0 9,815 0
Harbor porpoise............... Gulf of Alaska.. 5,484 0 27,420 0
Southeast Alaska 1,926 0 9,630 0
Dall's porpoise............... Alaska.......... 16,244 5 81,220 25
Cuvier's beaked whale......... Alaska.......... 2,544 0 12,720 0
Baird's beaked whale.......... Alaska.......... 401 0 2,005 0
Stejneger's beaked whale...... Alaska.......... 1,153 0 5,765 0
Steller sea lion.............. Eastern U.S..... 671 0 3,355 0
Western U.S..... 572 0 2,860 0
California sea lion........... U.S............. 5 0 25 0
Northern fur seal............. Eastern Pacific- 1,428 0 7,140 0
Alaska.
Northern elephant seal........ California 245 0 1,225 0
Breeding.
Harbor seal................... Aleutian Islands 0 0 0 0
Pribilof Islands 0 0 0 0
Bristol Bay..... 0 0 0 0
North Kodiak.... 1 0 5 0
South Kodiak.... 1 0 5 0
Prince William 2 0 10 0
Sound.
Cook Inlet/ 0 0 0 0
Shelikof.
Glacier Bay/Icy 0 0 0 0
Strait.
Lynn Canal/ 0 0 0 0
Stephens.
Harbor seal................... Sitka/Chatham... 0 0 0 0
Dixon/Cape 0 0 0 0
Decision.
Clarence Strait. 0 0 0 0
Ribbon seal................... Alaska.......... 0 0 0 0
---------------------------------------------------------------
Totals.................... ................ 36,522 5 182,610 25
----------------------------------------------------------------------------------------------------------------
Marine Mammal Habitat
The Navy's proposed training activities could potentially affect
marine mammal habitat through the introduction of sound into the water
column, impacts to the prey species of marine mammals, bottom
disturbance, or changes in water quality. Each of these components was
considered in the
[[Page 10001]]
GOA DSEIS/OEIS and was determined by the Navy to have no effect on
marine mammal habitat. Based on the information below and the
supporting information included in the GOA DSEIS/OEIS, NMFS has
preliminarily determined that the proposed training activities would
not have adverse or long-term impacts on marine mammal habitat.
Expected Effects on Habitat
Unless the sound source or explosive detonation is stationary and/
or continuous over a long duration in one area, the effects of the
introduction of sound into the environment are generally considered to
have a less severe impact on marine mammal habitat than the physical
alteration of the habitat. Acoustic exposures are not expected to
result in long-term physical alteration of the water column or bottom
topography, as the occurrences are of limited duration and are
intermittent in time. Surface vessels associated with the activities
are present in limited duration and are intermittent as they move
relatively rapidly through any given area. Most of the high-explosive
military expended materials would detonate at or near the water
surface. Only bottom-laid explosives are likely to affect bottom
substrate; habitat used for underwater detonations and seafloor device
placement would primarily be soft-bottom sediment. Once on the
seafloor, military expended material would likely be colonized by
benthic organisms because the materials would serve as anchor points in
the shifting bottom substrates, similar to a reef. The surface area of
bottom substrate affected would make up a very small percentage of the
total training area available in the Study Area.
Effects on Marine Mammal Prey
Invertebrates--Marine invertebrate distribution in the Study Area
is influenced by habitat, ocean currents, and water quality factors
such as temperature, salinity, and nutrient content (Levinton 2009).
The distribution of invertebrates is also influenced by their distance
from the equator (latitude); in general, the number of marine
invertebrate species increases toward the equator (Macpherson 2002).
The higher number of species (diversity) and abundance of marine
invertebrates in coastal habitats, compared with the open ocean, is a
result of more nutrient availability from terrestrial environments and
the variety of habitats and substrates found in coastal waters
(Levinton 2009).
The GOA is one of the world's most productive ocean regions and the
habitats associated with these cold and turbulent waters contain
identifiable collections of macrohabitats that sustain a multitude of
invertebrate species. Invertebrates in the GOA provide valuable links
in the food chain and perform ecosystem functions such as nutrient
processing. For humans, invertebrates contribute to economic, cultural,
and recreational activities in the GOA.
All marine invertebrate taxonomic groups are represented in the
Study Area. Major invertebrate phyla and the general zones they inhabit
in the Study Area are described in Chapter 3 of the 2011 GOA FEIS/OEIS.
Very little is known about sound detection and use of sound by
aquatic invertebrates (Budelmann 2010; Montgomery et al., 2006; Popper
et al., 2001). Organisms may detect sound by sensing either the
particle motion or pressure component of sound, or both. Aquatic
invertebrates probably do not detect pressure since many are generally
the same density as water and few, if any, have air cavities that would
function like the fish swim bladder in responding to pressure
(Budelmann, 2010; Popper et al., 2001). Many marine invertebrates,
however, have ciliated ``hair'' cells that may be sensitive to water
movements, such as those caused by currents or water particle motion
very close to a sound source (Budelmann, 2010; Mackie and Singla,
2003). These cilia may allow invertebrates to sense nearby prey or
predators or help with local navigation. Marine invertebrates may
produce and use sound in territorial behavior, to deter predators, to
find a mate, and to pursue courtship (Popper et al., 2001).
Both behavioral and auditory brainstem response studies suggest
that crustaceans may sense sounds up to three kilohertz (kHz), but best
sensitivity is likely below 200 Hz (Lovell et al., 2005; Lovell et al.,
2006; Goodall et al., 1990). Most cephalopods (e.g., octopus and squid)
likely sense low-frequency sound below 1,000 Hz, with best
sensitivities at lower frequencies (Budelmann, 2010; Mooney et al.,
2010; Packard et al., 1990). A few cephalopods may sense higher
frequencies up to 1,500 Hz (Hu et al., 2009). Squid did not respond to
toothed whale ultrasonic echolocation clicks at sound pressure levels
ranging from 199 to 226 dB re 1 [mu]Pa peak-to-peak, likely because
these clicks were outside of squid hearing range (Wilson et al., 2007).
However, squid exhibited alarm responses when exposed to broadband
sound from an approaching seismic airgun with received levels exceeding
145 to 150 dB re 1 [mu]Pa root mean square (McCauley et al., 2000b).
Little information is available on the potential impacts on marine
invertebrates of exposure to sonar, explosions, and other sound-
producing activities. It is expected that most marine invertebrates
would not sense mid- or high-frequency sounds, distant sounds, or
aircraft noise transmitted through the air-water interface. Most marine
invertebrates would not be close enough to intense sound sources, such
as some sonars, to potentially experience impacts to sensory
structures. Any marine invertebrate capable of sensing sound may alter
its behavior if exposed to non-impulsive sound, although it is unknown
if responses to non-impulsive sounds occur. Continuous noise, such as
from vessels, may contribute to masking of relevant environmental
sounds, such as reef noise. Because the distance over which most marine
invertebrates are expected to detect any sounds is limited and vessels
would be in transit, any sound exposures with the potential to cause
masking or behavioral responses would be brief and long-term impacts
are not expected. Although non-impulsive underwater sounds produced
during training activities may briefly impact individuals, intermittent
exposures to non-impulsive sounds are not expected to impact survival,
growth, recruitment, or reproduction of widespread marine invertebrate
populations.
Detonations associated with the Navy's GOA TMAA activities would
occur well offshore (the middle of the GOA TMAA is 140 nm offshore;
except for a point near Cape Cleare on Montague Island [12 nm away],
the nearest shoreline [Kenai Peninsula] is 24 nm north of the GOA TMAA
northern boundary). As water depth increases away from shore, benthic
invertebrates would be less likely to be impacted by detonations at or
near the surface. In addition, detonations near the surface would
release a portion of their explosive energy into the air, reducing the
explosive impacts in the water. Some marine invertebrates may be
sensitive to the low-frequency component of impulsive sound, and they
may exhibit startle reactions or temporary changes in swim speed in
response to an impulsive exposure. Because exposures are brief, limited
in number, and spread over a large area, no long-term impacts due to
startle reactions or short-term behavioral changes are expected.
Although individual marine invertebrates may be injured or killed
during an explosion or pile driving, no long-term impacts on
[[Page 10002]]
the survival, growth, recruitment, or reproduction of marine
invertebrate populations are expected.
Fish--Fish are not distributed uniformly throughout the Study Area,
but are closely associated with a variety of habitats. Some species
range across thousands of square miles while others have small home
ranges and restricted distributions (Helfman et al., 2009). The
movements of some open-ocean species may never overlap with coastal
fishes that spend their lives within several hundred feet (a few
hundred meters) of the shore. Even within a single fish species, the
distribution and specific habitats in which individuals occur may be
influenced by its developmental stage, size, sex, reproductive
condition, and other factors.
The distribution and abundance of fishes depends greatly on the
physical and biological factors of the marine ecosystem, such as
salinity, temperature, dissolved oxygen, population dynamics, predator
and prey interaction oscillations, seasonal movements, reproduction and
life cycles, and recruitment success (Helfman et al., 1997). A single
factor is rarely responsible for the distribution of fish species; more
often, a combination of factors is accountable. For example, open ocean
species optimize their growth, reproduction, and survival by tracking
gradients of temperature, oxygen, or salinity (Helfman et al., 1997).
Another major component in understanding species distribution is the
location of highly productive regions, such as frontal zones. These
areas concentrate various prey species and their predators, such as
tuna, and provide visual cues for the location of target species for
commercial fisheries (NMFS, 2001).
At least 383 species belonging to 84 families of marine and
anadromous fishes have been reported from the predominant ecosystems
found in the GOA TMAA. Detailed information on taxa presence,
distribution, and characteristics are provided in Chapter 3 of the 2011
GOA FEIS/OEIS.
All fish have two sensory systems to detect sound in the water: The
inner ear, which functions very much like the inner ear in other
vertebrates, and the lateral line, which consists of a series of
receptors along the fish's body (Popper, 2008). The inner ear generally
detects relatively higher-frequency sounds, while the lateral line
detects water motion at low frequencies (below a few hundred Hz)
(Hastings and Popper, 2005a). Although hearing capability data only
exist for fewer than 100 of the 32,000 fish species, current data
suggest that most species of fish detect sounds from 50 to 1,000 Hz,
with few fish hearing sounds above 4 kHz (Popper, 2008). It is believed
that most fish have their best hearing sensitivity from 100 to 400 Hz
(Popper, 2003b). Additionally, some clupeids (shad in the subfamily
Alosinae) possess ultrasonic hearing (i.e., able to detect sounds above
100,000 Hz) (Astrup, 1999). Permanent hearing loss, or permanent
threshold shift has not been documented in fish. The sensory hair cells
of the inner ear in fish can regenerate after they are damaged, unlike
in mammals where sensory hair cells loss is permanent (Lombarte et al.,
1993; Smith et al., 2006). As a consequence, any hearing loss in fish
may be as temporary as the timeframe required to repair or replace the
sensory cells that were damaged or destroyed (e.g., Smith et al.,
2006).
Potential direct injuries from non-impulsive sound sources, such as
sonar, are unlikely because of the relatively lower peak pressures and
slower rise times than potentially injurious sources such as
explosives. Non-impulsive sources also lack the strong shock waves
associated with an explosion. Therefore, direct injury is not likely to
occur from exposure to non-impulsive sources such as sonar, vessel
noise, or subsonic aircraft noise. Only a few fish species are able to
detect high-frequency sonar and could have behavioral reactions or
experience auditory masking during these activities. These effects are
expected to be transient and long-term consequences for the population
are not expected. MFAS is unlikely to impact fish species because most
species are unable to detect sounds in this frequency range and vessels
operating MFAS would be transiting an area (not stationary). While a
large number of fish species may be able to detect low-frequency sonar
and other active acoustic sources, low-frequency active usage is rare
and mostly conducted in deeper waters. Overall effects to fish from
non-impulsive sound sources would be localized and infrequent.
Physical effects from pressure waves generated by underwater sounds
(e.g. underwater explosions) could potentially affect fish within
proximity of training activities. In particular, the rapid oscillation
between high- and low-pressure peaks has the potential to burst the
swim bladders and other gas-containing organs of fish (Keevin and
Hemen, 1997). Sublethal effects, such as changes in behavior of fish,
have been observed in several occasions as a result of noise produced
by explosives (National Research Council of the National Academies,
2003; Wright, 1982). If an individual fish were repeatedly exposed to
sounds from underwater explosions that caused alterations in natural
behavioral patterns or physiological stress, these impacts could lead
to long-term consequences for the individual such as reduced survival,
growth, or reproductive capacity. However, the time scale of individual
explosions is very limited, and training exercises involving explosions
are dispersed in space and time. Consequently, repeated exposure of
individual fish to sounds from underwater explosions is not likely and
most acoustic effects are expected to be short-term and localized.
Long-term consequences for populations would not be expected.
Marine Mammal Avoidance
Marine mammals may be temporarily displaced from areas where Navy
training is occurring, but the area should be utilized again after the
activities have ceased. Avoidance of an area can help the animal avoid
further acoustic effects by avoiding or reducing further exposure. The
intermittent or short duration of many activities should prevent
animals from being exposed to stressors on a continuous basis (for the
GOA TMAA, training activities will not occur continuously throughout
the year, but rather, for a maximum of 21 days either once or twice
annually). In areas of repeated and frequent acoustic disturbance, some
animals may habituate or learn to tolerate the new baseline or
fluctuations in noise level. While some animals may not return to an
area, or may begin using an area differently due to training
activities, most animals are expected to return to their usual
locations and behavior.
Other Expected Effects
Other sources that may affect marine mammal habitat were considered
in the GOA DSEIS/OEIS and potentially include the introduction of fuel,
debris, ordnance, and chemical residues into the water column. The
majority of high-order explosions would occur at or above the surface
of the ocean, and would have no impacts on sediments and minimal
impacts on water quality. While disturbance or strike from an item
falling through the water column is possible, it is unlikely because
(1) objects sink slowly, (2) most projectiles are fired at targets (and
hit those targets), and (3) animals are generally widely dispersed
throughout the water column and over the Study Area. Chemical,
physical, or biological changes in sediment or water quality would not
be detectable. In the event of an ordnance failure, the energetic
materials it contained would remain mostly intact. The explosive
materials
[[Page 10003]]
in failed ordnance items and metal components from training would leach
slowly and would quickly disperse in the water column. Chemicals from
other explosives would not be introduced into the water column in large
amounts and all torpedoes would be recovered following training
activities, reducing the potential for chemical concentrations to reach
levels that can affect sediment quality, water quality, or benthic
habitats.
Preliminary Analysis and Negligible Impact Determination
Negligible impact is ``an impact resulting from the specified
activity that cannot be reasonably expected to, and is not reasonably
likely to, adversely affect the species or stock through effects on
annual rates of recruitment or survival'' (50 CFR 216.103). A
negligible impact finding is based on the lack of likely adverse
effects on annual rates of recruitment or survival (i.e., population-
level effects). An estimate of the number of takes, alone, is not
enough information on which to base an impact determination, as the
severity of harassment may vary greatly depending on the context and
duration of the behavioral response, many of which would not be
expected to have deleterious impacts on the fitness of any individuals.
In determining whether the expected takes will have a negligible
impact, in addition to considering estimates of the number of marine
mammals that might be ``taken,'' NMFS must consider other factors, such
as the likely nature of any responses (their intensity, duration,
etc.), the context of any responses (critical reproductive time or
location, migration, etc.), as well as the number and nature (e.g.,
severity) of estimated Level A harassment takes, the number of
estimated mortalities, and the status of the species. As a reminder,
the GOA TMAA training activities will not occur continuously throughout
the year, but rather, for a maximum of 21 days either once or twice
annually).
The Navy's specified activities have been described based on best
estimates of the maximum amount of sonar and other acoustic source use
or detonations that the Navy would conduct. There may be some
flexibility in that the exact number of hours, items, or detonations
may vary from year to year, but take totals are not authorized to
exceed the 5-year totals indicated in Tables 12-13. We base our
analysis and NID on the maximum number of takes authorized, although,
as stated before, the number of takes are only a part of the analysis,
which includes extensive qualitative consideration of other contextual
factors that influence the degree of impact of the takes on the
effected individuals. To avoid repetition, we provide some general
analysis immediately below that applies to all the species listed in
Tables 13, given that some of the anticipated effects (or lack thereof)
of the Navy's training activities on marine mammals are expected to be
relatively similar in nature. However, below that, we break our
analysis into species, or groups of species where relevant similarities
exist, to provide more specific information related to the anticipated
effects on individuals or where there is information about the status
or structure of any species that would lead to a differing assessment
of the effects on the population.
The Navy's take request is based on its model and post-model
analysis. In the discussions below, the ``acoustic analysis'' refers to
the Navy's modeling results and post-model analysis. The model
calculates sound energy propagation from sonar, other active acoustic
sources, and explosives during naval activities; the sound or impulse
received by animat dosimeters representing marine mammals distributed
in the area around the modeled activity; and whether the sound or
impulse received by a marine mammal exceeds the thresholds for effects.
The model estimates are then further analyzed to consider animal
avoidance and implementation of highly effective mitigation measures to
prevent Level A harassment, resulting in final estimates of effects due
to Navy training and testing. NMFS provided input to the Navy on this
process and the Navy's qualitative analysis is described in detail in
Chapter 6 of its LOA application (https://www.nmfs.noaa.gov/pr/permits/incidental/militry.htm).
Generally speaking, and especially with other factors being equal,
the Navy and NMFS anticipate more severe effects from takes resulting
from exposure to higher received levels (though this is in no way a
strictly linear relationship throughout species, individuals, or
circumstances) and less severe effects from takes resulting from
exposure to lower received levels. The requested number of Level B
takes does not equate to the number of individual animals the Navy
expects to harass (which is lower), but rather to the instances of take
(i.e., exposures above the Level B harassment threshold) that would
occur. Additionally, these instances may represent either a very brief
exposure (seconds) or, in some cases, longer durations of exposure
within a day. Depending on the location, duration, and frequency of
activities, along with the distribution and movement of marine mammals,
individual animals may be exposed to impulse or non-impulse sounds at
or above the Level B harassment threshold on multiple days. However,
the Navy is currently unable to estimate the number of individuals that
may be taken during training and testing activities. The model results
estimate the total number of takes that may occur to a smaller number
of individuals. While the model shows that an increased number of
exposures may take place due to an increase in events/activities and
ordnance, the types and severity of individual responses to training
and testing activities are not expected to change.
Behavioral Harassment
As discussed previously in this proposed rule, marine mammals can
respond to LF/MFAS/HFAS in many different ways, a subset of which
qualifies as behavioral harassment. As described in the proposed rule,
the Navy uses the behavioral response function to quantify the number
of behavioral responses that would qualify as Level B behavioral
harassment under the MMPA. As the statutory definition is currently
applied, a wide range of behavioral reactions may qualify as Level B
harassment under the MMPA, including but not limited to avoidance of
the sound source, temporary changes in vocalizations or dive patterns,
temporary avoidance of an area, or temporary disruption of feeding,
migrating, or reproductive behaviors.
Some of the lower level physiological stress responses discussed
earlier would also likely co-occur with the predicted harassments,
although these responses are more difficult to detect and fewer data
exist relating these responses to specific received levels of sound.
Level B takes, then, may have a stress-related physiological component
as well; however, we would not expect the Navy's generally short-term,
intermittent, and (in the case of sonar) transitory activities to
create conditions of long-term, continuous noise leading to long-term
physiological stress responses in marine mammals.
The estimates calculated using the behavioral response function do
not differentiate between the different types of potential reactions.
Nor do the estimates provide information regarding the potential
fitness or other biological consequences of the reactions on the
affected individuals. We therefore consider the available scientific
evidence to determine the likely nature of the modeled behavioral
responses and the potential fitness consequences for affected
individuals.
[[Page 10004]]
For LF/MFAS/HFAS use in the GOA TMAA, the Navy provided information
(Table 14) estimating the percentage of behavioral harassment that
would occur within the 6-dB bins (without considering mitigation or
avoidance). As mentioned above, an animal's exposure to a higher
received level is more likely to result in a behavioral response that
is more likely to adversely affect the health of the animal. As
illustrated below, the majority (including about 72 percent for the
most powerful ASW hull-mounted sonar, which is responsible for a large
portion of the sonar takes) of calculated takes from MFAS result from
exposures less than 156 dB. Less than 1 percent of the takes are
expected to result from exposures above 174 dB. Specifically, given a
range of behavioral responses that may be classified as Level B
harassment, to the degree that higher received levels are expected to
result in more severe behavioral responses, only a small percentage of
the anticipated Level B harassment from Navy activities might
necessarily be expected to potentially result in more severe responses,
especially when the distance from the source at which the levels below
are received is considered (see Table 14). Marine mammals are able to
discern the distance of a given sound source, and given other equal
factors (including received level), they have been reported to respond
more to sounds that are closer (DeRuiter et al., 2013). Further, the
estimated number of responses do not reflect either the duration or
context of those anticipated responses, some of which will be of very
short duration, and other factors should be considered when predicting
how the estimated takes may affect individual fitness. A recent study
by Moore and Barlow (2013) emphasizes the importance of context (e.g.,
behavioral state of the animals, distance from the sound source, etc.)
in evaluating behavioral responses of marine mammals to acoustic
sources.
Table 14--Non-Impulsive Ranges in 6-dB bins and Percentage of Behavioral Harassments
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sonar bin MF1 (e.g., SQS-53; ASW Sonar bin MF4 (e.g., AQS-22; ASW Sonar Bin MF5 (e.g., SSQ-62; ASW
hull mounted sonar) dipping sonar) sonobuoy)
-----------------------------------------------------------------------------------------------------------------
Percentage of Percentage of Percentage of
Received level Distance at which behavioral Distance at which behavioral Distance at which behavioral
levels occur harassments levels occur harassments levels occur harassments
within radius of occurring at within radius of occurring at within radius of occurring at
source (m) given levels source (m) given levels source (m) given levels
--------------------------------------------------------------------------------------------------------------------------------------------------------
Low Frequency Cetaceans
--------------------------------------------------------------------------------------------------------------------------------------------------------
120 <= SPL <126....................... 178,750-156,450 0.00 100,000-92,200 0.00 22,800-15,650 0.00
126 <= SPL <132....................... 156,450-147,500 0.00 92,200-55,050 0.11 15,650-11,850 0.05
132 <= SPL <138....................... 147,500-103,700 0.21 55,050-46,550 1.08 11,850-6,950 2.84
138 <= SPL <144....................... 103,700-97,950 0.33 46,550-15,150 35.69 6,950-3,600 16.04
144 <= SPL <150....................... 97,950-55,050 13.73 15,150-5,900 26.40 3,600-1,700 33.63
150 <= SPL <156....................... 55,050-49,900 5.28 5,900-2,700 17.43 1,700-250 44.12
156 <= SPL <162....................... 49,900-10,700 72.62 2,700-1,500 9.99 250-100 2.56
162 <= SPL <168....................... 10,700-4,200 6.13 1,500-200 9.07 100-<50 0.76
168 <= SPL <174....................... 4,200-1,850 1.32 200-100 0.18 <50 0.00
174 <= SPL <180....................... 1,850-850 0.30 100-<50 0.05 <50 0.00
180 <= SPL <186....................... 850-400 0.07 <50 0.00 <50 0.00
186 <= SPL <192....................... 400-200 0.01 <50 0.00 <50 0.00
192 <= SPL <198....................... 200-100 0.00 <50 0.00 <50 0.00
--------------------------------------------------------------------------------------------------------------------------------------------------------
Mid Frequency Cetaceans
--------------------------------------------------------------------------------------------------------------------------------------------------------
120 <= SPL <126....................... 179,400-156,450 0.00 100,000-92,200 0.00 23,413-16,125 0.00
126 <= SPL <132....................... 156,450-147,500 0.00 92,200-55,050 0.11 16,125-11,500 0.06
132 <= SPL <138....................... 147,500-103,750 0.21 55,050-46,550 1.08 11,500-6,738 2.56
138 <= SPL <144....................... 103,750-97,950 0.33 46,550-15,150 35.69 6,738-3,825 13.35
144 <= SPL <150....................... 97,950-55,900 13.36 15,150-5,900 26.40 3,825-1,713 37.37
150 <= SPL <156....................... 55,900-49,900 6.12 5,900-2,700 17.43 1,713-250 42.85
156 <= SPL <162....................... 49,900-11,450 71.18 2,700-1,500 9.99 250-150 1.87
162 <= SPL <168....................... 11,450-4,350 7.01 1,500-200 9.07 150-<50 1.93
168 <= SPL <174....................... 4,350-1,850 1.42 200-100 0.18 <50 0.00
174 <= SPL <180....................... 1,850-850 0.29 100-<50 0.05 <50 0.00
180 <= SPL <186....................... 850-400 0.07 <50 0.00 <50 0.00
186 <= SPL <192....................... 400-200 0.01 <50 0.00 <50 0.00
192 <= SPL <198....................... 200-100 0.00 <50 0.00 <50 0.00
--------------------------------------------------------------------------------------------------------------------------------------------------------
Notes: (1) ASW = anti-submarine warfare, m = meters, SPL = sound pressure level; (2) Odontocete behavioral response function is also used for high-
frequency cetaceans, phocid seals, otariid seals and sea lions, and sea otters.
Although the Navy has been monitoring to discern the effects of LF/
MFAS/HFAS on marine mammals since 2006, and research on the effects of
MFAS is advancing, our understanding of exactly how marine mammals in
the Study Area will respond to LF/MFAS/HFAS is still improving. The
Navy has submitted more than 80 reports, including Major Exercise
Reports, Annual Exercise Reports, and Monitoring Reports, documenting
hundreds of thousands of marine mammals across Navy range complexes,
and there are only two instances of overt behavioral disturbances that
have been observed. One cannot conclude from these results that marine
mammals were not harassed from MFAS/HFAS, as a portion of animals
within the area of concern were not seen (especially those more
cryptic, deep-diving species, such as beaked whales or Kogia spp.), the
full series of behaviors that would more accurately show an important
change is not typically seen (i.e., only the surface behaviors are
observed), and some of the non-biologist watchstanders might not be
well-qualified to characterize behaviors. However, one can say that the
animals that were observed did not respond in any of the obviously more
severe ways, such as panic, aggression, or anti-predator response.
[[Page 10005]]
Diel Cycle
As noted previously, many animals perform vital functions, such as
feeding, resting, traveling, and socializing on a diel cycle (24-hour
cycle). Behavioral reactions to noise exposure (when taking place in a
biologically important context, such as disruption of critical life
functions, displacement, or avoidance of important habitat) are more
likely to be significant if they last more than one diel cycle or recur
on subsequent days (Southall et al., 2007). Consequently, a behavioral
response lasting less than one day and not recurring on subsequent days
is not considered severe unless it could directly affect reproduction
or survival (Southall et al., 2007). Note that there is a difference
between multiple-day substantive behavioral reactions and multiple-day
anthropogenic activities. For example, just because an at-sea exercise
lasts for multiple days does not necessarily mean that individual
animals are either exposed to those exercises for multiple days or,
further, exposed in a manner resulting in a sustained multiple day
substantive behavioral response. Large multi-day Navy exercises, such
as those proposed in the GOA TMAA, typically include vessels that are
continuously moving at speeds typically 10-15 knots, or higher, and
likely cover large areas that are relatively far from shore, in
addition to the fact that marine mammals are moving as well, which
would make it unlikely that the same animal could remain in the
immediate vicinity of the ship for the entire duration of the exercise.
Additionally, the Navy does not necessarily operate active sonar the
entire time during an exercise. While it is certainly possible that
these sorts of exercises could overlap with individual marine mammals
multiple days in a row at levels above those anticipated to result in a
take, because of the factors mentioned above, it is considered unlikely
for the majority of takes. It does not mean that a behavioral response
is necessarily sustained for multiple days, but instead necessitates
the consideration of likely duration and context to assess any effects
on the individual's fitness.
Durations for non-impulsive activities utilizing tactical sonar
sources vary and are fully described in Appendix A of the GOA DSEIS/
OEIS. ASW training exercises using MFAS/HFAS proposed for the GOA TMAA
generally last for 2-16 hours, and may have intervals of non-activity
in between. Because of the need to train in a large variety of
situations (in the case of the GOA TMAA, complex bathymetric and
oceanographic conditions include a continental shelf, submarine
canyons, seamounts, and fresh water infusions from multiple sources),
the Navy does not typically conduct successive ASW exercises in the
same locations. Given the average length of ASW exercises (times of
continuous sonar use) and typical vessel speed, combined with the fact
that the majority of the cetaceans in the GOA TMAA Study Area would not
likely remain in an area for successive days, it is unlikely that an
animal would be exposed to MFAS/HFAS at levels likely to result in a
substantive response that would then be carried on for more than one
day or on successive days.
With the exception of SINKEXs, the planned explosive exercises for
the GOA TMAA are of a short duration (1-6 hours). Although explosive
exercises may sometimes be conducted in the same general areas
repeatedly, because of their short duration and the fact that they are
in the open ocean and animals can easily move away, it is similarly
unlikely that animals would be exposed for long, continuous amounts of
time. Although SINKEXs may last for up to 48 hrs, only two are planned
annually for the GOA TMAA training activities, they are stationary and
conducted in deep, open water (where fewer marine mammals would
typically be expected to be randomly encountered), and they have a
rigorous monitoring and shutdown procedures, all of which make it
unlikely that individuals would be exposed to the exercise for extended
periods or on consecutive days.
TTS
As mentioned previously, TTS can last from a few minutes to days,
be of varying degree, and occur across various frequency bandwidths,
all of which determine the severity of the impacts on the affected
individual, which can range from minor to more severe. The TTS
sustained by an animal is primarily classified by three
characteristics:
1. Frequency--Available data (of mid-frequency hearing specialists
exposed to mid- or high-frequency sounds; Southall et al., 2007)
suggest that most TTS occurs in the frequency range of the source up to
one octave higher than the source (with the maximum TTS at \1/2\ octave
above). The more powerful MF sources used have center frequencies
between 3.5 and 8 kHz and the other unidentified MF sources are, by
definition, less than 10 kHz, which suggests that TTS induced by any of
these MF sources would be in a frequency band somewhere between
approximately 2 and 20 kHz. There are fewer hours of HF source use and
the sounds would attenuate more quickly, plus they have lower source
levels, but if an animal were to incur TTS from these sources, it would
cover a higher frequency range (sources are between 20 and 100 kHz,
which means that TTS could range up to 200 kHz; however, HF systems are
typically used less frequently and for shorter time periods than
surface ship and aircraft MF systems, so TTS from these sources is even
less likely). TTS from explosives would be broadband. Vocalization data
for each species, which would inform how TTS might specifically
interfere with communications with conspecifics, was provided in the
LOA application.
2. Degree of the shift (i.e., by how many dB the sensitivity of the
hearing is reduced)--Generally, both the degree of TTS and the duration
of TTS will be greater if the marine mammal is exposed to a higher
level of energy (which would occur when the peak dB level is higher or
the duration is longer). The threshold for the onset of TTS was
discussed previously in this proposed rule. An animal would have to
approach closer to the source or remain in the vicinity of the sound
source appreciably longer to increase the received SEL, which would be
difficult considering the Lookouts and the nominal speed of an active
sonar vessel (10-15 knots). In the TTS studies (see Threshold Shift
section), some using exposures of almost an hour in duration or up to
217 SEL, most of the TTS induced was 15 dB or less, though Finneran et
al. (2007) induced 43 dB of TTS with a 64-second exposure to a 20 kHz
source. However, MFAS emits a ping typically every 50 seconds, and
incurring those levels of TTS is highly unlikely.
3. Duration of TTS (recovery time)--In the TTS laboratory studies
(see Threshold Shift section), some using exposures of almost an hour
in duration or up to 217 SEL, almost all individuals recovered within 1
day (or less, often in minutes), although in one study (Finneran et
al., 2007), recovery took 4 days.
Based on the range of degree and duration of TTS reportedly induced
by exposures to non-pulse sounds of energy higher than that to which
free-swimming marine mammals in the field are likely to be exposed
during MFAS/HFAS training exercises in the GOA TMAA, it is unlikely
that marine mammals would ever sustain a TTS from MFAS that alters
their sensitivity by more than 20 dB for more than a few days (and any
incident of TTS would likely be far less severe due to the short
duration of the majority of the exercises and the speed of a typical
vessel). Also, for the same reasons discussed in the Diel Cycle
section, and because of the
[[Page 10006]]
short distance within which animals would need to approach the sound
source, it is unlikely that animals would be exposed to the levels
necessary to induce TTS in subsequent time periods such that their
recovery is impeded. Additionally, though the frequency range of TTS
that marine mammals might sustain would overlap with some of the
frequency ranges of their vocalization types, the frequency range of
TTS from MFAS (the source from which TTS would most likely be sustained
because the higher source level and slower attenuation make it more
likely that an animal would be exposed to a higher received level)
would not usually span the entire frequency range of one vocalization
type, much less span all types of vocalizations or other critical
auditory cues. If impaired, marine mammals would typically be aware of
their impairment and are sometimes able to implement behaviors to
compensate (see Acoustic Masking or Communication Impairment section),
though these compensations may incur energetic costs.
Acoustic Masking or Communication Impairment
Masking only occurs during the time of the signal (and potential
secondary arrivals of indirect rays), versus TTS, which continues
beyond the duration of the signal. Standard MFAS typically pings every
50 seconds for hull-mounted sources. For the sources for which we know
the pulse length, most are significantly shorter than hull-mounted
active sonar, on the order of several microseconds to tens of
microseconds. For hull-mounted active sonar, though some of the
vocalizations that marine mammals make are less than one second long,
there is only a 1 in 50 chance that they would occur exactly when the
ping was received, and when vocalizations are longer than one second,
only parts of them are masked. Alternately, when the pulses are only
several microseconds long, the majority of most animals' vocalizations
would not be masked. Masking effects from MFAS/HFAS are expected to be
minimal. If masking or communication impairment were to occur briefly,
it would be in the frequency range of MFAS, which overlaps with some
marine mammal vocalizations; however, it would likely not mask the
entirety of any particular vocalization, communication series, or other
critical auditory cue, because the signal length, frequency, and duty
cycle of the MFAS/HFAS signal does not perfectly mimic the
characteristics of any marine mammal's vocalizations. The other sources
used in Navy training and testing, many of either higher frequencies
(meaning that the sounds generated attenuate even closer to the source)
or lower amounts of operation, are similarly not expected to result in
masking.
PTS, Injury, or Mortality
NMFS believes that many marine mammals would deliberately avoid
exposing themselves to the received levels of active sonar necessary to
induce injury by moving away from or at least modifying their path to
avoid a close approach. Additionally, in the unlikely event that an
animal approaches the sonar vessel at a close distance, NMFS believes
that the mitigation measures (i.e., shutdown/powerdown zones for MFAS/
HFAS) would typically ensure that animals would not be exposed to
injurious levels of sound. As discussed previously, the Navy utilizes
both aerial (when available) and passive acoustic monitoring (during
all ASW exercises) in addition to watchstanders on vessels to detect
marine mammals for mitigation implementation.
If a marine mammal is able to approach a surface vessel within the
distance necessary to incur PTS, the likely speed of the vessel
(nominal 10-15 knots) would make it very difficult for the animal to
remain in range long enough to accumulate enough energy to result in
more than a mild case of PTS. As mentioned previously and in relation
to TTS, the likely consequences to the health of an individual that
incurs PTS can range from mild to more serious dependent upon the
degree of PTS and the frequency band it is in, and many animals are
able to compensate for the shift, although it may include energetic
costs. Only 5 Level A (PTS) takes per year are predicted from GOA
training activities, and these are all Dall's porpoise--not large whale
species or beaked whales. We also assume that the acoustic exposures
sufficient to trigger onset PTS (or TTS) would be accompanied by
physiological stress responses, although the sound characteristics that
correlate with specific stress responses in marine mammals are poorly
understood. As discussed above for Behavioral Harassment, we would not
expect the Navy's generally short-term, intermittent, and (in the case
of sonar) transitory activities to create conditions of long-term,
continuous noise leading to long-term physiological stress responses in
marine mammals. No other injurious takes or mortality are predicted. As
discussed previously, marine mammals (especially beaked whales) could
potentially respond to MFAS at a received level lower than the injury
threshold in a manner that indirectly results in the animals stranding.
The exact mechanism of this potential response, behavioral or
physiological, is not known. When naval exercises have been associated
with strandings in the past, it has typically been when three or more
vessels are operating simultaneously, in the presence of a strong
surface duct, and in areas of constricted channels, semi-enclosed
areas, and/or steep bathymetry. While these features certainly do not
define the only factors that can contribute to a stranding, and while
they need not all be present in their aggregate to increase the
likelihood of a stranding, it is worth noting that they are not all
present in the GOA TMAA, which only has a strong surface duct present
during the winter, and does not have bathymetry or constricted channels
of the type that have been present in the sonar associated strandings.
When this is combined with consideration of the number of hours of
active sonar training that will be conducted and the total duration of
all training exercises (a maximum of 21 days once or twice a year), we
believe that the probability is small that this will occur. Lastly, an
active sonar shutdown protocol for strandings involving live animals
milling in the water minimizes the chances that these types of events
turn into mortalities.
As stated previously, there have been no recorded Navy vessel
strikes of any marine mammals during training in the GOA Study Area to
date, nor were takes by injury or mortality resulting from vessel
strike predicted in the Navy's analysis.
Group and Species-Specific Analysis
Predicted effects on marine mammals from exposures to sonar and
other active acoustic sources and explosions during annual training
activities are shown in Table 13. The vast majority of predicted
exposures (greater than 99 percent) are expected to be Level B
harassment (non-injurious TTS and behavioral reactions) from sonar and
other active acoustic sources at relatively low received levels (Table
14). The acoustic analysis predicts the majority of marine mammal
species in the Study Area would not be exposed to explosive (impulsive)
sources associated with training activities. Only Dall's porpoise is
predicted to have Level B (TTS) exposures resulting from explosives,
and only a limited number (5) of Dall's porpoise are expected to have
injurious take (PTS) resulting from sonar and other active acoustic
sources and
[[Page 10007]]
explosions. There are no lethal takes predicted for any marine mammal
species for the GOA activities.
The analysis below may in some cases (e.g., mysticetes, porpoises,
pinnipeds) address species collectively if they occupy the same
functional hearing group (i.e., low-, mid-, and high-frequency
cetaceans and pinnipeds in water), have similar hearing capabilities,
and/or are known to generally behaviorally respond similarly to
acoustic stressors. Where there are meaningful differences between
species or stocks in anticipated individual responses to activities,
impact of expected take on the population due to differences in
population status, or impacts on habitat, they will either be described
within the section or the species will be included as a separate sub-
section.
Mysticetes--The Navy's acoustic analysis predicts that 2,923
instances of Level B harassmant of mysticete whales may occur in the
Study Area each year from sonar and other active acoustic sources
during training activities. Annual species-specific take estimates are
as follows: 7 North Pacific right whales (Eastern North Pacific stock),
139 humpback whales (Central North Pacific and Western North Pacific
stocks), 95 blue whales (Eastern North Pacific stock), 2,582 fin whales
(Northeast Pacific stock), 13 sei whales (Eastern North Pacific stock),
and 87 minke whales (Alaska stock). Of these species, humpback, blue,
fin, sei, and North Pacific right whales are listed as endangered under
the ESA and depleted under the MMPA. NMFS is currently engaged in an
internal Section 7 consultation under the ESA and the outcome of that
consultation will further inform our final decision. Based on the
distribution information presented in the LOA application, it is highly
unlikely that gray whales would be encountered in the Study Area during
events involving use of sonar and other active acoustic sources. The
acoustic analysis did not predict any takes of gray whales and NMFS is
not authorizing any takes of this species.
Generally, these represent a limited number of takes relative to
population estimates for most mysticete stocks in the Study Area (Table
6). When the numbers of behavioral takes are compared to the estimated
stock abundance and if one assumes that each take happens to a separate
animal, less than approximately 20 percent of each of these stocks
(with the exception of the Northeast Pacific stock of fin whale and the
Alaska stock of minke whale for which there currently are no reliable
population estimates because only portions of the stocks' range have
been surveyed [Muto and Angliss, 2015]) would be behaviorally harassed
during the course of a year. Because the estimates given above
represent the total number of exposures and not necessarily the number
of individuals exposed, it is more likely that fewer individuals would
be taken, but a subset would be taken more than one time per year. In
the ocean, the use of sonar and other active acoustic sources is
transient and is unlikely to repeatedly expose the same population of
animals over a short period.
Level B harassment takes are anticipated to be in the form of TTS
and behavioral reactions and no injurious takes of North Pacific right,
humpback, blue, fin, minke, or sei whales from sonar and other active
acoustic stressors or explosives are expected. The majority of acoustic
effects to mysticetes from sonar and other active sound sources during
training activities would be primarily from anti-submarine warfare
events involving surface ships and hull mounted sonar. Research and
observations show that if mysticetes are exposed to sonar or other
active acoustic sources they may react in a number of ways depending on
the characteristics of the sound source, their experience with the
sound source, and whether they are migrating or on seasonal grounds
(i.e., breeding or feeding). Reactions may include alerting, breaking
off feeding dives and surfacing, diving or swimming away, or no
response at all (Richardson, 1995; Nowacek, 2007; Southall et al.,
2007; Finneran and Jenkins, 2012). Richardson et al. (1995) noted that
avoidance (temporary displacement of an individual from an area)
reactions are the most obvious manifestations of disturbance in marine
mammals. Avoidance is qualitatively different from the startle or
flight response, but also differs in the magnitude of the response
(i.e., directed movement, rate of travel, etc.). Oftentimes avoidance
is temporary, and animals return to the area once the noise has ceased.
Additionally, migrating animals may ignore a sound source, or divert
around the source if it is in their path.
Specific to U.S. Navy systems using low frequency sound, studies
were undertaken in 1997-98 pursuant to the Navy's Low Frequency Sound
Scientific Research Program. These studies found only short-term
responses to low frequency sound by mysticetes (fin, blue, and humpback
whales) including changes in vocal activity and avoidance of the source
vessel (Clark, 2001; Miller et al., 2000; Croll et al., 2001; Fristrup
et al., 2003; Nowacek et al., 2007). Baleen whales exposed to moderate
low-frequency signals demonstrated no variation in foraging activity
(Croll et al., 2001). Low-frequency signals of the Acoustic Thermometry
of Ocean Climate sound source were not found to affect dive times of
humpback whales in Hawaiian waters (Frankel and Clark, 2000).
Specific to mid-frequency sound, studies by Melc[oacute]n et al.
(2012) in the Southern California Bight found that the likelihood of
blue whale low-frequency calling (usually associated with feeding
behavior) decreased with an increased level of MFAS, beginning at a SPL
of approximately 110-120 dB re 1 [mu]Pa. However, it is not known
whether the lower rates of calling actually indicated a reduction in
feeding behavior or social contact since the study used data from
remotely deployed, passive acoustic monitoring buoys. Results from the
2010-2011 field season of an ongoing behavioral response study in
Southern California waters indicated that in some cases and at low
received levels, tagged blue whales responded to MFAS but that those
responses were mild and there was a quick return to their baseline
activity (Southall et al., 2011; Southall et al., 2012b). Blue whales
responded to a mid-frequency sound source, with a source level between
160 and 210 dB re 1 [mu]Pa at 1 m and a received sound level up to 160
dB re 1 [mu]Pa, by exhibiting generalized avoidance responses and
changes to dive behavior during the exposure experiments (CEE)
(Goldbogen et al., 2013). However, reactions were not consistent across
individuals based on received sound levels alone, and likely were the
result of a complex interaction between sound exposure factors such as
proximity to sound source and sound type (MFAS simulation vs. pseudo-
random noise), environmental conditions, and behavioral state. Surface
feeding whales did not show a change in behavior during CEEs, but deep
feeding and non-feeding whales showed temporary reactions that quickly
abated after sound exposure. Distances of the sound source from the
whales during CEEs were sometimes less than a mile. Blue whales have
been documented exhibiting a range of foraging strategies for
maximizing feeding dependent on the density of their prey at a given
location (Goldbogen et al., 2015), so it may be that a temporary
behavioral reaction or avoidance of a location where feeding was
occurring is not meaningful to the life history of an animal. The
preliminary findings from Goldbogen et al. (2013) and Melc[oacute]n et
al. (2012) are generally consistent with
[[Page 10008]]
the Navy's criteria and thresholds for predicting behavioral effects to
mysticetes from sonar and other active acoustic sources used in the
quantitative acoustic effects analysis for GOA. The Navy's behavioral
response function predicts the probability of a behavioral response
that rises to a Level B take for individuals exposed to a received SPL
of 120 dB re 1 [mu]Pa or greater, with an increasing probability of
reaction with increased received level as demonstrated in Melc[oacute]n
et al. (2012).
High-frequency systems are notably outside of mysticetes' ideal
hearing and vocalization range and it is unlikely that they would cause
a significant behavioral reaction.
Most Level B harassments to mysticetes from sonar in the Study Area
would result from received levels less than 156 dB SPL. Therefore, the
majority of Level B takes are expected to be in the form of milder
responses (i.e., lower-level exposures that still rise to the level of
take, but would likely be less severe in the range of responses that
qualify as take) of a generally short duration. As mentioned earlier in
this section, we anticipate more severe effects from takes when animals
are exposed to higher received levels. Most low-frequency (mysticetes)
cetaceans observed in studies usually avoided sound sources at levels
of less than or equal to 160 dB re 1[mu]Pa. Occasional milder
behavioral reactions are unlikely to cause long-term consequences for
individual animals or populations. Even if sound exposure were to be
concentrated in a relatively small geographic area over a long period
of time (e.g., days or weeks during major training exercises), we would
expect that some individual whales would avoid areas where exposures to
acoustic stressors are at higher levels. For example, Goldbogen et al.
(2013) indicated some horizontal displacement of deep foraging blue
whales in response to simulated MFA sonar. Given these animal's
mobility and large ranges, we would expect these individuals to
temporarily select alternative foraging sites nearby until the exposure
levels in their initially selected foraging area have decreased.
Therefore, even temporary displacement from initially selected foraging
habitat is not expected to impact the fitness of any individual animals
because we would expect equivalent foraging to be available in close
proximity. Because we do not expect any fitness consequences from any
individual animals, we do not expect any population level effects from
these behavioral responses.
As explained above, recovery from a threshold shift (TTS) can take
a few minutes to a few days, depending on the exposure duration, sound
exposure level, and the magnitude of the initial shift, with larger
threshold shifts and longer exposure durations requiring longer
recovery times (Finneran et al., 2005; Finneran and Schlundt, 2010;
Mooney et al., 2009a; Mooney et al., 2009b). However, large threshold
shifts are not anticipated for these activities because of the
unlikelihood that animals will remain within the ensonified area (due
to the short duration of the majority of exercises, the speed of the
vessels, and the short distance within which the animal would need to
approach the sound source) at high levels for the duration necessary to
induce larger threshold shifts. Threshold shifts do not necessarily
affect all hearing frequencies equally, so some threshold shifts may
not interfere with an animal's hearing of biologically relevant sounds.
Furthermore, the implementation of mitigation and the sightability of
mysticetes (due to their large size) reduces the potential for a
significant behavioral reaction or a threshold shift to occur.
Overall, the number of predicted behavioral reactions is low and
occasional behavioral reactions are unlikely to cause long-term
consequences for individual animals or populations. This assessment of
long-term consequences is based in part on findings from ocean areas
where the Navy has been intensively training and testing with sonar and
other active acoustic sources for decades. While there are many factors
such as the end of large-scale commercial whaling complicating any
analysis, there is no data suggesting any long-term consequences to
mysticetes from exposure to sonar and other active acoustic sources. On
the contrary, there are findings suggesting mysticete populations are
increasing in the two primary locations (Southern California and
Hawaii) where the Navy's most intensively used range complexes are
located. These findings include: (1) Calambokidis et al. (2009b)
indicating a significant upward trend in abundance of for blue whales
in Southern California; (2) the recovery of gray whales that migrate
through the Navy's SOCAL Range Complex twice a year; (3) work by Moore
and Barlow (2011) indicating evidence of increasing fin whale abundance
in the California Current area, which includes the SOCAL Range Complex;
(4) the range expansion and increasing presence of Bryde's whales south
of Point Conception in Southern California (Kerosky et al. 2012); and
(5) the ocean area contained within the Hawaii Range Complex continuing
to function as a critical breeding, calving, and nursing area to the
point at which the overall humpback whale population in the North
Pacific is now greater than some prior estimates of pre-whaling
abundance (Barlow et al., 2011). The implementation of mitigation and
the sightability of mysticetes (due to their large size) reduces the
potential for a significant behavioral reaction or a threshold shift to
occur. Furthermore, there is no designated critical habitat for
mysticetes in the Study Area. As discussed in the Consideration of
Time/Area Limitations section of this rule, review of the NMFS-
identified feeding and migration areas showed there is only minimal (<1
percent) spatial overlap with the GOA TMAA and the North Pacific right
whale feeding area southeast of Kodiak Island and minimal (<1 percent)
spatial overlap with a small portion of the gray whale migration area
offshore of Kenai Peninsula (Ferguson et al., 2015b). Those areas of
overlap at the corners of the GOA TMAA are very unlikely to have any
Navy training activity. Further, the grey whale migration area is only
applicable in the early spring and late fall, while training activities
are proposed for May to October (with June/July the main months of
training, historically). Therefore, it is very unlikely there would be
an effect to feeding or migrating activities if right whales or gray
whales were present. Additionally, appropriate mitigation measures (as
detailed in the Mitigation section above) would be implemented for any
detected marine mammals and thus further reducing the potential for the
feeding or migration activities to be affected. The Navy proposes to
monitor use of active sonar within the North Pacific right whale
feeding area and gray whale migration areas, to the extent that active
sonar training does occur in these areas, and to report that use to
NMFS in classified annual reports (see Proposed Reporting) to inform
future adaptive management of activities within the GOA TMAA.
Consequently, the GOA TMAA activities are not expected to adversely
impact rates of recruitment or survival of mysticete whales.
Sperm Whales--The Navy's acoustic analysis indicates that 197
instances of Level B harassment of sperm whales (North Pacific stock;
currently there are no reliable abundance estimates for this stock
[Muto and Angliss, 2015]) may occur in the Study Area each year from
sonar or other active acoustic stressors during training activities.
Sperm whales are listed as endangered under the ESA
[[Page 10009]]
and depleted under the MMPA. NMFS is currently engaged in an internal
Section 7 consultation under the ESA and the outcome of that
consultation will further inform our final decision. These Level B
takes are anticipated to be in the form of TTS and behavioral reactions
and no injurious takes of sperm whales from sonar and other active
acoustic stressors or explosives are requested or proposed for
authorization. Sperm whales have shown resilience to acoustic and human
disturbance, although they may react to sound sources and activities
within a few kilometers. Sperm whales that are exposed to activities
that involve the use of sonar and other active acoustic sources may
alert, ignore the stimulus, avoid the area by swimming away or diving,
or display aggressive behavior (Richardson, 1995; Nowacek, 2007;
Southall et al., 2007; Finneran and Jenkins, 2012). Some (but not all)
sperm whale vocalizations might overlap with the MFAS/HFAS TTS
frequency range, which could temporarily decrease an animal's
sensitivity to the calls of conspecifics or returning echolocation
signals. However, as noted previously, NMFS does not anticipate TTS of
a long duration or severe degree to occur as a result of exposure to
MFAS/HFAS. Recovery from a threshold shift (TTS) can take a few minutes
to a few days, depending on the exposure duration, sound exposure
level, and the magnitude of the initial shift, with larger threshold
shifts and longer exposure durations requiring longer recovery times
(Finneran et al., 2005; Mooney et al., 2009a; Mooney et al., 2009b;
Finneran and Schlundt, 2010). Large threshold shifts are not
anticipated for these activities because of the unlikelihood that
animals will remain within the ensonified area (due to the short
duration of the majority of exercises, the speed of the vessels, and
the short distance within which the animal would need to approach the
sound source) at high levels for the duration necessary to induce
larger threshold shifts. Threshold shifts do not necessarily affect all
hearing frequencies equally, so some threshold shifts may not interfere
with an animal's hearing of biologically relevant sounds. No sperm
whales are predicted to be exposed to MFAS/HFAS sound levels associated
with PTS or injury.
The majority of Level B takes are expected to be in the form of
mild responses (low-level exposures) and of a generally short duration.
Relative to the population size, this activity is anticipated to result
only in a limited number of Level B harassment takes. Because the
estimates given above represent the total number of exposures and not
necessarily the number of individuals exposed, it is more likely that
fewer individuals would be taken, but a subset would be taken more than
one time per year. In the ocean, the use of sonar and other active
acoustic sources is transient and is unlikely to repeatedly expose the
same population of animals over a short period. Overall, the number of
predicted behavioral reactions are unlikely to cause long-term
consequences for individual animals or populations. The GOA activities
are not expected to occur in an area/time of specific importance for
reproductive, feeding, or other known critical behaviors for sperm
whales, and there is no designated critical habitat in the Study Area.
Consequently, the activities are not expected to adversely impact
annual rates of recruitment or survival of sperm whales.
Dolphins and Small Whales--The Navy's acoustic analysis predicts
the following instances of Level B harassment of delphinids (dolphins
and small whales) each year from sonar and other active acoustic
sources associated with training activities in the Study Area: 762
killer whales (Alaska Resident; Eastern North Pacific Offshore; AT1
Transient; and GOA, Aleutian Island, and Bearing Sea Transient stocks)
and 1,963 Pacific white-sided dolphins (North Pacific stock). These
represent a limited number of takes relative to population estimates
for delphinid stocks in the Study Area (Table 6). When the numbers of
behavioral takes are compared to the estimated stock abundance and if
one assumes that each take happens to a separate animal, less than 25
percent of each of the killer whale stocks and less than 8 percent of
the North Pacific stock of Pacific white-sided dolphin would be
behaviorally harassed during the course of a year. More likely,
slightly fewer individuals would be harassed, but a subset would be
harassed more than one time during the course of the year.
All of these takes are anticipated to be in the form of behavioral
harassment (TTS and behavioral reaction) and no injurious takes of
delphinids from sonar and other active acoustic stressors or explosives
are requested or proposed for authorization. Further, the majority of
takes are anticipated to be by behavioral harassment in the form of
mild responses. Research and observations show that if delphinids are
exposed to sonar or other active acoustic sources they may react in a
number of ways depending on their experience with the sound source and
what activity they are engaged in at the time of the acoustic exposure.
Delphinids may not react at all until the sound source is approaching
within a few hundred meters to within a few kilometers depending on the
environmental conditions and species. Delphinids that are exposed to
activities that involve the use of sonar and other active acoustic
sources may alert, ignore the stimulus, change their behaviors or
vocalizations, avoid the sound source by swimming away or diving, or be
attracted to the sound source (Richardson, 1995; Nowacek, 2007;
Southall et al., 2007; Finneran and Jenkins, 2012). Research has
demonstrated that Alaska Resident killer whales may routinely move over
long large distances (Andrews and Matkin, 2014; Fearnbach et al.,
2013). In a similar documented long-distance movement, an Eastern North
Pacific Offshore stock killer whale tagged off San Clemente Island,
California, moved (over a period of 147 days) to waters off northern
Mexico, then north to Cook Inlet, Alaska, and finally (when the tag
ceased transmitting) to coastal waters off Southeast Alaska (Falcone
and Schorr, 2014). Given these findings, temporary displacement due to
avoidance of training activities are therefore unlikely to have
biological significance to individual animals.
Delphinid species generally travel in large pods and should be
visible from a distance in order to implement mitigation measures and
reduce potential impacts. Many of the recorded delphinid vocalizations
overlap with the MFAS/HFAS TTS frequency range (2-20 kHz); however, as
noted above, NMFS does not anticipate TTS of a serious degree or
extended duration to occur as a result of exposure to MFAS/HFAS.
Recovery from a threshold shift (TTS) can take a few minutes to a few
days, depending on the exposure duration, sound exposure level, and the
magnitude of the initial shift, with larger threshold shifts and longer
exposure durations requiring longer recovery times (Finneran et al.,
2005; Finneran and Schlundt, 2010; Mooney et al., 2009a; Mooney et al.,
2009b). However, large threshold shifts are not anticipated for these
activities because of the unlikelihood that animals will remain within
the ensonified area (due to the short duration of the majority of
exercises, the speed of the vessels, and the short distance within
which the animal would need to approach the sound source) at high
levels for the duration necessary to induce larger threshold shifts.
Threshold shifts do not necessarily affect all hearing frequencies
equally, so some threshold shifts may
[[Page 10010]]
not interfere with an animal's hearing of biologically relevant sounds.
Their size and detectability makes it unlikely that these animals would
be exposed to the higher energy or pressure expected to result in more
severe effects.
The predicted effects to delphinids are unlikely to cause long-term
consequences for individual animals or populations. The GOA TMAA
activities are not expected to occur in an area/time of specific
importance for reproductive, feeding, or other known critical behaviors
for delphinids. Stocks of delphinid species found in the Study Area are
not depleted under the MMPA, nor are they listed under the ESA.
Consequently, the activities are not expected to adversely impact rates
of recruitment or survival of delphinid species.
Porpoises--The Navy's acoustic analysis predicts that 16,244
instances of Level B harassment (TTS and behavioral) of Dall's porpoise
(Alaska stock) and 7,410 instances of Level B harassment of harbor
porpoise (GOA and Southeast Alaska stocks) may occur each year from
sonar and other active acoustic sources and explosives associated with
training and testing activities in the Study Area. These represent a
limited number of takes relative to population estimates for porpoise
stocks in the Study Area (Table 6). When the numbers of takes for
Dall's and harbor porpoise are compared to their respective estimated
stock abundances and if one assumes that each take happens to a
separate animal, less than 20 percent of the Alaska stock of Dall's
porpoise, and less than 18 percent of the GOA and Southeast Alaska
stocks of harbor porpoise would be harassed (behaviorally) during the
course of a year. Because the estimates given above represent the total
number of exposures and not necessarily the number of individuals
exposed, it is more likely that fewer individuals would be taken, but a
subset would be taken more than one time per year.
Behavioral responses can range from a mild orienting response, or a
shifting of attention, to flight and panic (Richardson, 1995; Nowacek,
2007; Southall et al., 2007). Acoustic analysis (factoring in the post-
model correction for avoidance and mitigation) also predicted that 5
Dall's porpoises might be exposed to sound levels from sonar and other
active acoustic stressors and explosives likely to result in PTS or
injury (Level A harassment).
The number of Dall's and harbor porpoise behaviorally harassed by
exposure to MFAS/HFAS in the Study Area is generally higher than the
other species. This is due to the low Level B harassment threshold (we
assume for the purpose of estimating take that all harbor porpoises
exposed to 120 dB or higher MFAS/HFAS will be taken by Level B
behavioral harassment), which essentially makes the ensonified area of
effects significantly larger than for the other species. However, the
fact that the threshold is a step function and not a curve (and
assuming uniform density) means that the vast majority of the takes
occur in the very lowest levels that exceed the threshold (it is
estimated that approximately 80 percent of the takes are from exposures
to 120 dB-126 dB), which means that anticipated behavioral effects are
not expected to be severe (e.g., temporary avoidance). As mentioned
above, an animal's exposure to a higher received level is more likely
to result in a behavioral response that is more likely to adversely
affect the health of an animal. Animals that do not exhibit a
significant behavioral reaction would likely recover from any incurred
costs, which reduces the likelihood of long-term consequences, such as
reduced fitness, for the individual or population.
Animals that experience hearing loss (TTS or PTS) may have reduced
ability to detect relevant sounds such as predators, prey, or social
vocalizations. Some porpoise vocalizations might overlap with the MFAS/
HFAS TTS frequency range (2-20 kHz). Recovery from a threshold shift
(TTS; partial hearing loss) can take a few minutes to a few days,
depending on the exposure duration, sound exposure level, and the
magnitude of the initial shift, with larger threshold shifts and longer
exposure durations requiring longer recovery times (Finneran et al.,
2005; Mooney et al., 2009a; Mooney et al., 2009b; Finneran and
Schlundt, 2010). More severe shifts may not fully recover and thus
would be considered PTS. However, large degrees of PTS are not
anticipated for these activities because of the unlikelihood that
animals will remain within the ensonified area (due to the short
duration of the majority of exercises, the speed of the vessels, and
the short distance within which the animal would need to approach the
sound source) at high levels for the duration necessary to induce
larger threshold shifts. Threshold shifts do not necessarily affect all
hearing frequencies equally, so some threshold shifts may not interfere
with an animal hearing biologically relevant sounds. The likely
consequences to the health of an individual that incurs PTS can range
from mild to more serious, depending upon the degree of PTS and the
frequency band it is in, and many animals are able to compensate for
the shift, although it may include energetic costs. Furthermore, likely
avoidance of intense activity and sound coupled with mitigation
measures would further reduce the potential for severe PTS exposures to
occur. If a marine mammal is able to approach a surface vessel within
the distance necessary to incur PTS, the likely speed of the vessel
(nominal 10-15 knots) would make it very difficult for the animal to
remain in range long enough to accumulate enough energy to result in
more than a mild case of PTS.
Harbor porpoises have been observed to be especially sensitive to
human activity (Tyack et al., 2011; Pirotta et al., 2012). The
information currently available regarding harbor porpoises suggests a
very low threshold level of response for both captive (Kastelein et
al., 2000; Kastelein et al., 2005) and wild (Johnston, 2002) animals.
Southall et al. (2007) concluded that harbor porpoises are likely
sensitive to a wide range of anthropogenic sounds at low received
levels (~ 90 to 120 dB). Research and observations of harbor porpoises
for other locations show that this small species is wary of human
activity and will display profound avoidance behavior for anthropogenic
sound sources in many situations at levels down to 120 dB re 1
[micro]Pa (Southall, 2007). Harbor porpoises routinely avoid and swim
away from large motorized vessels (Barlow et al., 1988; Evans et al.,
1994; Palka and Hammond, 2001; Polacheck and Thorpe, 1990). The
vaquita, which is closely related to the harbor porpoise in the Study
Area, appears to avoid large vessels at about 2,995 ft. (913 m)
(Jaramillo-Legorreta et al., 1999). The assumption is that the harbor
porpoise would respond similarly to large Navy vessels, possibly prior
to commencement of sonar or explosive activity (i.e., pre-activity
avoidance). Harbor porpoises may startle and temporarily leave the
immediate area of the training or testing until after the event ends.
ASW training exercises using MFAS/HFAS generally last for 2-16
hours, and may have intervals of non-activity in between. In addition,
the Navy does not typically conduct ASW exercises in the same
locations. Given the average length of ASW exercises (times of
continuous sonar use) and typical vessel speed, combined with the fact
that the majority of porpoises in the Study Area would not likely
remain in an area for successive days, it is unlikely that an animal
would be exposed to MFAS/HFAS at levels likely to result in a
substantive response (e.g., interruption
[[Page 10011]]
of feeding) that would then be carried on for more than one day or on
successive days. Thompson et al. (2013) showed that seismic surveys
conducted over a 10-day period in the North Sea did not result in the
broad-scale displacement of harbor porpoises away from preferred
habitat. The harbor porpoises were observed to leave the area at the
onset of survey, but returned within a few hours, and the overall
response of the porpoises decreased over the 10-day period.
Considering the information above, the predicted effects to Dall's
and harbor porpoise are unlikely to cause long-term consequences for
individual animals or the population. The GOA activities are not
expected to occur in an area/time of specific importance for
reproductive, feeding, or other known critical behaviors for Dall's and
harbor porpoise. Stocks of Dall's and harbor porpoise are not listed as
depleted under the MMPA. Consequently, the activities are not expected
to adversely impact annual rates of recruitment or survival of
porpoises.
Beaked Whales--Acoustic analysis predicts that 401 Baird's beaked
whales (Alaska stock), 2,544 Cuvier's beaked whales (Alaska stock), and
1,153 Stejneger's beaked whales (Alaska stock) will be taken annually
by Level B harassment from exposure to sonar and other active acoustic
stressors. These takes are anticipated to be in the form of behavioral
harassment (mainly behavioral reaction and some TTS) and no injurious
takes of beaked whales from sonar and other active acoustic stressors
or explosives are requested or proposed. Relative to population size,
training activities are anticipated to result only in a limited number
of takes. Because the estimates given above represent the total number
of exposures and not necessarily the number of individuals exposed, it
is more likely that fewer individuals would be taken, but a subset
would be taken more than one time per year. There are currently no
reliable abundance estimates for Alaska stocks of Baird's, Cuvier's,
and Stejner's beaked whales (Muto and Angliss, 2015).
As is the case with harbor porpoises, beaked whales have been shown
to be particularly sensitive to sound and therefore have been assigned
a lower harassment threshold based on observations of wild animals by
McCarthy et al. (2011) and Tyack et al. (2011). The fact that the Level
B harassment threshold is a step function (The Navy has adopted an
unweighted 140 dB re 1 [micro]Pa SPL threshold for significant
behavioral effects for all beaked whales) and not a curve (and assuming
uniform density) means that the vast majority of the takes occur in the
very lowest levels that exceed the threshold (it is estimated that
approximately 80 percent of the takes are from exposures to 140 dB to
146 dB), which means that the anticipated effects for the majority of
exposures are not expected to be severe (As mentioned above, an
animal's exposure to a higher received level is more likely to result
in a behavioral response that is more likely to adversely affect the
health of an animal). Further, Moretti et al. (2014) recently derived
an empirical risk function for Blainville's beaked whale that predicts
there is a 0.5 probability of disturbance at a received level of 150 dB
(CI: 144-155), suggesting that in some cases the current Navy step
function may over-estimate the effects of an activity using sonar on
beaked whales. Irrespective of the Moretti et al. (2014) risk function,
NMFS' analysis assumes that all of the beaked whale Level B takes that
are proposed for authorization will occur, and we base our negligible
impact determination, in part, on the fact that these exposures would
mainly occur at the very lowest end of the 140-dB behavioral harassment
threshold where behavioral effects are expected to be much less severe
and generally temporary in nature.
Behavioral responses can range from a mild orienting response, or a
shifting of attention, to flight and panic (Richardson, 1995; Nowacek,
2007; Southall et al., 2007; Finneran and Jenkins, 2012). Research has
also shown that beaked whales are especially sensitive to the presence
of human activity (Tyack et al., 2011; Pirotta et al., 2012). Beaked
whales have been documented to exhibit avoidance of human activity or
respond to vessel presence (Pirotta et al., 2012). Beaked whales were
observed to react negatively to survey vessels or low altitude aircraft
by quick diving and other avoidance maneuvers, and none were observed
to approach vessels (Wursig et al., 1998). Some beaked whale
vocalizations may overlap with the MFAS/HFAS TTS frequency range (2-20
kHz); however, as noted above, NMFS does not anticipate TTS of a
serious degree or extended duration to occur as a result of exposure to
MFA/HFAS. Recovery from a threshold shift (TTS) can take a few minutes
to a few days, depending on the exposure duration, sound exposure
level, and the magnitude of the initial shift, with larger threshold
shifts and longer exposure durations requiring longer recovery times
(Finneran et al., 2005; Mooney et al., 2009a; Mooney et al., 2009b;
Finneran and Schlundt, 2010). Large threshold shifts are not
anticipated for these activities because of the unlikelihood that
animals will remain within the ensonified area (due to the short
duration of the majority of exercises, the speed of the vessels, and
the short distance within which the animal would need to approach the
sound source) at high levels for the duration necessary to induce
larger threshold shifts. Threshold shifts do not necessarily affect all
hearing frequencies equally, so some threshold shifts may not interfere
with an animal's hearing of biologically relevant sounds.
It has been speculated for some time that beaked whales might have
unusual sensitivities to sonar sound due to their likelihood of
stranding in conjunction with MFAS use. Research and observations show
that if beaked whales are exposed to sonar or other active acoustic
sources they may startle, break off feeding dives, and avoid the area
of the sound source to levels of 157 dB re 1 [micro]Pa, or below
(McCarthy et al., 2011). Acoustic monitoring during actual sonar
exercises revealed some beaked whales continuing to forage at levels up
to 157 dB re 1 [micro]Pa (Tyack et al. 2011). Stimpert et al. (2014)
tagged a Baird's beaked whale, which was subsequently exposed to
simulated MFAS. Changes in the animal's dive behavior and locomotion
were observed when received level reached 127 dB re 1[mu]Pa. However,
Manzano-Roth et al. (2013) found that for beaked whale dives that
continued to occur during MFAS activity, differences from normal dive
profiles and click rates were not detected with estimated received
levels up to 137 dB re 1 [micro]Pa while the animals were at depth
during their dives. And in research done at the Navy's fixed tracking
range in the Bahamas, animals were observed to leave the immediate area
of the anti-submarine warfare training exercise (avoiding the sonar
acoustic footprint at a distance where the received level was ``around
140 dB'' SPL, according to Tyack et al. [2011]) but return within a few
days after the event ended (Claridge and Durban, 2009; Moretti et al.,
2009, 2010; Tyack et al., 2010, 2011; McCarthy et al., 2011). Tyack et
al. (2011) report that, in reaction to sonar playbacks, most beaked
whales stopped echolocating, made long slow ascent to the surface, and
moved away from the sound. A similar behavioral response study
conducted in Southern California waters during the 2010-2011 field
season found that Cuvier's beaked whales exposed to MFAS displayed
behavior ranging from initial orientation changes
[[Page 10012]]
to avoidance responses characterized by energetic fluking and swimming
away from the source (DeRuiter et al., 2013b). However, the authors did
not detect similar responses to incidental exposure to distant naval
sonar exercises at comparable received levels, indicating that context
of the exposures (e.g., source proximity, controlled source ramp-up)
may have been a significant factor. The study itself found the results
inconclusive and meriting further investigation. Cuvier's beaked whale
responses suggested particular sensitivity to sound exposure as
consistent with results for Blainville's beaked whale.
Populations of beaked whales and other odontocetes on the Bahamas
and other Navy fixed ranges that have been operating for decades,
appear to be stable. Behavioral reactions (avoidance of the area of
Navy activity) seem likely in most cases if beaked whales are exposed
to anti-submarine sonar within a few tens of kilometers, especially for
prolonged periods (a few hours or more) since this is one of the most
sensitive marine mammal groups to anthropogenic sound of any species or
group studied to date and research indicates beaked whales will leave
an area where anthropogenic sound is present (Tyack et al., 2011; De
Ruiter et al., 2013; Manzano-Roth et al., 2013; Moretti et al., 2014).
Research involving tagged Cuvier's beaked whales in the SOCAL Range
Complex reported on by Falcone and Schorr (2012, 2014) indicates year-
round prolonged use of the Navy's training and testing area by these
beaked whales and has documented movements in excess of hundreds of
kilometers by some of those animals. Given that some of these animals
may routinely move hundreds of kilometers as part of their normal
pattern, leaving an area where sonar or other anthropogenic sound is
present may have little, if any, cost to such an animal. Photo
identification studies in the SOCAL Range Complex, a Navy range that is
utilized for training and testing more frequently than the GOA TMAA
Study Area, have identified approximately 100 individual Cuvier's
beaked whale individuals with 40 percent having been seen in one or
more prior years, with re-sightings up to 7 years apart (Falcone and
Schorr, 2014). These results indicate long-term residency by
individuals in an intensively used Navy training and testing area,
which may also suggest a lack of long-term consequences as a result of
exposure to Navy training and testing activities. Finally, results from
passive acoustic monitoring estimated regional Cuvier's beaked whale
densities were higher than indicated by the NMFS's broad scale visual
surveys for the U.S. west coast (Hildebrand and McDonald, 2009).
Based on the findings above, it is clear that the Navy's long-term
ongoing use of sonar and other active acoustic sources has not
precluded beaked whales from also continuing to inhabit those areas. In
summary, based on the best available science, the Navy and NMFS believe
that beaked whales that exhibit a significant TTS or behavioral
reaction due to sonar and other active acoustic testing activities
would generally not have long-term consequences for individuals or
populations. Claridge (2013) speculated that sonar use in a Bahamas
range could have ``a possible population-level effect'' on beaked
whales based on lower abundance in comparison to control sites. In
summary, Claridge suggested that lower reproductive rates observed at
the Navy's Atlantic Undersea Test and Evaluation Center (AUTEC), when
compared to a control site, were due to stressors associated with
frequent and repeated use of Navy sonar. It is also important to note
that there were some relevant shortcomings of this study. For example,
all of the re-sighted whales during the 5-year study at both sites were
female, which Claridge acknowledged can lead to a negative bias in the
abundance estimation. There was also a reduced effort and shorter
overall study period at the AUTEC site that failed to capture some of
the emigration/immigration trends identified at the control site.
Furthermore, Claridge assumed that the two sites were identical and
therefore should have equal potential abundances; when in reality,
there were notable physical differences. The author also acknowledged
that ``information currently available cannot provide a quantitative
answer to whether frequent sonar use at [the Bahamas range] is causing
stress to resident beaked whales,'' and cautioned that the outcome of
ongoing studies ``is a critical component to understanding if there are
population-level effects.'' Moore and Barlow (2013) have noted a
decline in beaked whale populations in a broad area of the Pacific
Ocean area out to 300 nm from the coast and extending from the
Canadian-U.S. border to the tip of Baja Mexico. There are scientific
caveats and limitations to the data used for that analysis, as well as
oceanographic and species assemblage changes on the U.S. Pacific coast
not thoroughly addressed. Although Moore and Barlow (2013) have noted a
decline in the overall beaked whale population along the Pacific coast,
in the small fraction of that area where the Navy has been training and
testing with sonar and other systems for decades (the Navy's SOCAL
Range Complex), higher densities and long-term residency by individual
Cuvier's beaked whales suggest that the decline noted elsewhere is not
apparent where Navy sonar use is most intense. Navy sonar training and
testing is not conducted along a large part of the U.S. west coast from
which Moore and Barlow (2013) drew their survey data. In Southern
California, based on a series of surveys from 2006 to 2008 and a high
number encounter rate, Falcone et al. (2009) suggested the ocean basin
west of San Clemente Island may be an important region for Cuvier's
beaked whales given the number of animals encountered there. Follow-up
research (Falcone and Schorr, 2012, 2014) in this same location
suggests that Cuvier's beaked whales may have population sub-units with
higher than expected residency, particularly in the Navy's instrumented
Southern California Anti-Submarine Warfare Range. Encounters with
multiple groups of Cuvier's and Baird's beaked whales indicated not
only that they were prevalent on the range where Navy routinely trains
and tests, but also that they were potentially present in much higher
densities than had been reported for anywhere along the U.S. west coast
(Falcone et al., 2009, Falcone and Schorr, 2012). This finding is also
consistent with concurrent results from passive acoustic monitoring
that estimated regional Cuvier's beaked whale densities were higher
where Navy trains in the SOCAL training and testing area than indicated
by NMFS's broad scale visual surveys for the U.S. west coast
(Hildebrand and McDonald, 2009).
NMFS also considered New et al. (2013) and their mathematical model
simulating a functional link between foraging energetics and
requirements for survival and reproduction for 21 species of beaked
whales. However, NMFS concluded that New et al. (2013) model lacks
critical data and accurate inputs necessary to form valid conclusions
specifically about impacts of anthropogenic sound from Navy activities
on beaked whale populations. The study itself notes the need for
``future research,'' identifies ``key data needs'' relating to input
parameters that ``particularly affected'' the model results, and states
only that the use of the model ``in combination with more detailed
research'' could help predict the effects of management actions on
beaked whale species. In short,
[[Page 10013]]
information is not currently available to specifically support the use
of this model in a project-specific evaluation of the effects of Navy
activities on the impacted beaked whale species in GOA.
No beaked whales are predicted in the acoustic analysis to be
exposed to sound levels associated with PTS, other injury, or
mortality. After decades of the Navy conducting similar activities in
the GOA Study Area without incident, NMFS does not expect strandings,
injury, or mortality of beaked whales to occur as a result of training
activities. Stranding events coincident with Navy MFAS use in which
exposure to sonar is believed to have been a contributing factor were
detailed in the Stranding and Mortality section of this proposed rule.
However, for some of these stranding events, a causal relationship
between sonar exposure and the stranding could not be clearly
established (Cox et al., 2006). In other instances, sonar was
considered only one of several factors that, in their aggregate, may
have contributed to the stranding event (Freitas, 2004; Cox et al.,
2006). Because of the association between tactical MFAS use and a small
number of marine mammal strandings, the Navy and NMFS have been
considering and addressing the potential for strandings in association
with Navy activities for years. In addition to a suite of mitigation
measures intended to more broadly minimize impacts to marine mammals,
the reporting requirements set forth in this rule ensure that NMFS is
notified immediately (or as soon as clearance procedures allow) if a
stranded marine mammal is found during or shortly after, and in the
vicinity of, any Navy training exercise utilizing MFAS, HFAS, or
underwater explosive detonations (see General Notification of Injured
or Dead Marine Mammals and the Stranding Response Plan in the
regulatory text below). Additionally, through the MMPA process (which
allows for adaptive management), NMFS and the Navy will determine the
appropriate way to proceed in the event that a causal relationship were
to be found between Navy activities and a future stranding.
The GOA training activities are not expected to occur in an area/
time of specific importance for reproductive, feeding, or other known
critical behaviors for beaked whales. None of the Pacific stocks for
beaked whales species found in the Study Area are depleted under the
MMPA. The degree of predicted Level B harassment is expected to be
mild, and no beaked whales are predicted in the acoustic analysis to be
exposed to sound levels associated with PTS, other injury, or
mortality. Consequently, the activities are not expected to adversely
impact annual rates of recruitment or survival of beaked whales.
Pinnipeds--The Navy's acoustic analysis predicts that the following
numbers of Level B harassment (TTS and behavioral reaction) may occur
annually from sonar and other active acoustic stressors associated with
training activities: 1,243 Steller sea lions (Eastern U.S. and Western
U.S. stocks); 5 California sea lions (U.S. stock); 1,428 northern fur
seals (Eastern Pacific stock); 245 northern elephant seals (California
Breeding stock); and 4 harbor seals (North Kodiak, South Kodiak, and
Prince William Sound stocks). These represent a limited number of takes
relative to population estimates for pinniped stocks in the Study Area
(Table 6). When the numbers of behavioral takes are compared to the
estimated stock abundances, less than 2 percent of each of these stocks
would be behaviorally harassed during the course of a year. These
estimates represents the total number of exposures and not necessarily
the number of individuals exposed, as a single individual may be
exposed multiple times over the course of a year. Based on the
distribution information presented in the LOA application, it is highly
unlikely that ribbon seals would be encountered in the Study Area
during events involving use of sonar and other active acoustic sources
or explosives. The acoustic analysis did not predict any takes of
ribbon seals and NMFS is not authorizing any takes of this species.
Research has demonstrated that for pinnipeds, as for other mammals,
recovery from a threshold shift (TTS) can take a few minutes to a few
days, depending on the exposure duration, sound exposure level, and the
magnitude of the initial shift, with larger threshold shifts and longer
exposure durations requiring longer recovery times (Finneran et al.,
2005; Finneran and Schlundt, 2010; Mooney et al., 2009a; Mooney et al.,
2009b). However, large threshold shifts are not anticipated for these
activities because of the unlikelihood that animals will remain within
the ensonified area (due to the short duration of the majority of
exercises, the speed of the vessels, and the short distance within
which the animal would need to approach the sound source) at high
levels for the duration necessary to induce larger threshold shifts.
Threshold shifts do not necessarily affect all hearing frequencies
equally, so threshold shifts may not necessarily interfere with an
animal's ability to hear biologically relevant sounds.
Research and observations show that pinnipeds in the water may be
tolerant of anthropogenic noise and activity (a review of behavioral
reactions by pinnipeds to impulsive and non-impulsive noise can be
found in Richardson et al., 1995 and Southall et al., 2007). Available
data, though limited, suggest that exposures between approximately 90
and 140 dB SPL do not appear to induce strong behavioral responses in
pinnipeds exposed to nonpulse sounds in water (Jacobs and Terhune,
2002; Costa et al., 2003; Kastelein et al., 2006c). Based on the
limited data on pinnipeds in the water exposed to multiple pulses
(small explosives, impact pile driving, and seismic sources), exposures
in the approximately 150 to 180 dB SPL range generally have limited
potential to induce avoidance behavior in pinnipeds (Harris et al.,
2001; Blackwell et al., 2004; Miller et al., 2004). If pinnipeds are
exposed to sonar or other active acoustic sources they may react in a
number of ways depending on their experience with the sound source and
what activity they are engaged in at the time of the acoustic exposure.
Pinnipeds may not react at all until the sound source is approaching
within a few hundred meters and then may alert, ignore the stimulus,
change their behaviors, or avoid the immediate area by swimming away or
diving. Houser et al. (2013) performed a controlled exposure study
involving California sea lions exposed to a simulated MFAS signal. The
purpose of this Navy-sponsored study was to determine the probability
and magnitude of behavioral responses by California sea lions exposed
to differing intensities of simulated MFAS signals. Behavioral
reactions included increased respiration rates, prolonged submergence,
and refusal to participate, among others. Younger animals were more
likely to respond than older animals, while some sea lions did not
respond consistently at any level. Houser et al.'s findings are
consistent with current scientific studies and criteria development
concerning marine mammal reactions to MFAS. Effects on pinnipeds in the
Study Area that are taken by Level B harassment, on the basis of
reports in the literature as well as Navy monitoring from past
activities, will likely be limited to reactions such as increased
swimming speeds, increased surfacing time, or decreased foraging (if
such activity were occurring). Most likely, individuals will simply
move away from the sound source and be temporarily displaced from those
areas, or not respond at all. In areas of
[[Page 10014]]
repeated and frequent acoustic disturbance, some animals may habituate
or learn to tolerate the new baseline or fluctuations in noise level.
Habituation can occur when an animal's response to a stimulus wanes
with repeated exposure, usually in the absence of unpleasant associated
events (Wartzok et al., 2003). While some animals may not return to an
area, or may begin using an area differently due to training and
testing activities, most animals are expected to return to their usual
locations and behavior. Given their documented tolerance of
anthropogenic sound (Richardson et al., 1995 and Southall et al.,
2007), repeated exposures of individuals (e.g., harbor seals) to levels
of sound that may cause Level B harassment are unlikely to result in
hearing impairment or to significantly disrupt foraging behavior. As
stated above, pinnipeds may habituate to or become tolerant of repeated
exposures over time, learning to ignore a stimulus that in the past has
not accompanied any overt threat.
Thus, even repeated Level B harassment of some small subset of an
overall stock is unlikely to result in any significant realized
decrease in fitness to those individuals, and would not result in any
adverse impact to the stock as a whole. Evidence from areas where the
Navy extensively trains and tests provides some indication of the
possible consequences resulting from those proposed activities. In the
confined waters of Washington State's Hood Canal where the Navy has
been training and intensively testing for decades and harbor seals are
present year-round, the population level has remained stable suggesting
the area's carrying capacity likely has been reached (Jeffries et al.,
2003; Gaydos et al., 2013). Within Puget Sound there are several
locations where pinnipeds use Navy structures (e.g., submarines,
security barriers) for haulouts. Given that animals continue to choose
these areas for their resting behavior, it would appear there are no
long-term effects or consequences to those animals as a result of
ongoing and routine Navy activities.
Generally speaking, most pinniped stocks in the Study Area are
thought to be stable or increasing (Carretta et al., 2014, 2015).
Abundance estimates for pinniped stocks in the Study Area are shown in
Table 6. Relative to population size, training activities are
anticipated to result only in a limited number of takes. No areas of
specific importance for reproduction or feeding for pinnipeds have been
identified in the Study Area. Consequently, the activities are not
expected to adversely impact rates of recruitment or survival of
pinniped species.
Western U.S. stocks of Steller sea lions are listed as endangered
under the ESA; however, there is no designated critical habitat Steller
sea lions in the Study Area. As a conservative measure, the GOA TMAA
boundary zone was specifically drawn to exclude any nearby critical
habitat and associated terrestrial, air, or aquatic zones. NMFS is
currently engaged in an internal Section 7 consultation under the ESA
and the outcome of that consultation will further inform our final
determination.
Long-Term Consequences
The best assessment of long-term consequences from training
activities will be to monitor the populations over time within a given
Navy range complex. A U.S. workshop on Marine Mammals and Sound (Fitch
et al., 2011) indicated a critical need for baseline biological data on
marine mammal abundance, distribution, habitat, and behavior over
sufficient time and space to evaluate impacts from human-generated
activities on long-term population survival. The Navy has developed
monitoring plans for protected marine mammals occurring on Navy ranges
with the goal of assessing the impacts of training and testing
activities on marine species and the effectiveness of the Navy's
current mitigation practices. Continued monitoring efforts over time
will be necessary to completely evaluate the long-term consequences of
exposure to noise sources.
Since 2006 across all Navy range complexes (in the Atlantic, Gulf
of Mexico, and the Pacific), there have been more than 80 reports,
including Major Exercise Reports, Annual Exercise Reports, and
Monitoring Reports. For the Pacific since 2011, there have been 29
monitoring and exercise reports submitted to NMFS to further research
goals aimed at understanding the Navy's impact on the environment as it
carries out its mission to train and test.
In addition to this multi-year record of reports from across the
Navy, there have also been ongoing Behavioral Response Study research
efforts (in Southern California and the Bahamas) specifically focused
on determining the potential effects from Navy mid-frequency sonar
(Southall et al., 2011, 2012; McCarthy et al., 2011; Tyack et al.,
2011; DeRuiter et al., 2013b; Goldbogen et al., 2013; Moretti et al.,
2014). This multi-year compendium of monitoring, observation, study,
and broad scientific research is informative with regard to assessing
the effects of Navy training and testing in general. Given that this
record involves many of the same Navy training activities being
considered for the Study Area and because it includes all the marine
mammal taxonomic families and many of the same species, this compendium
of Navy reporting is directly applicable to assessing locations such as
the GOA TMAA.
In the Hawaii and Southern California Navy training and testing
ranges from 2009 to 2012, Navy-funded marine mammal monitoring research
completed over 5,000 hours of visual survey effort covering over 65,000
nautical miles, sighted over 256,000 individual marine mammals, took
over 45,600 digital photos and 36 hours of digital video, attached 70
satellite tracking tags to individual marine mammals, and collected
over 40,000 hours of passive acoustic recordings. In Hawaii alone
between 2006 and 2012, there were 21 scientific marine mammal surveys
conducted before, during, or after major exercises. This monitoring
effort is consistent with other research from these areas in that there
have been no direct evidence demonstration that routine Navy training
and testing has negatively impacted marine mammal populations
inhabiting these Navy ranges. Continued monitoring efforts over time
will be necessary to completely evaluate the long-term consequences of
exposure to noise sources. Other research findings related to the
general topic of long-term impacts are discussed above in the Species-
Specific Analysis.
Based on monitoring conducted before, during, and after Navy
training and testing events since 2006, the NMFS' assessment is that it
is unlikely there will be impacts having any long-term consequences to
populations of marine mammals as a result of the proposed continuation
of training and testing in the ocean areas historically used by the
Navy including the Study Area. This assessment of likelihood is based
on four indicators from areas in the Pacific where Navy training and
testing has been ongoing for decades: (1) Evidence suggesting or
documenting increases in the numbers of marine mammals present
(Calambokidis and Barlow, 2004; Falcone et al., 2009; Hildebrand and
McDonald, 2009; Falcone and Shorr, 2012; Calambokidis et al., 2009a;
Berman-Kowalewski et al., 2010; Moore and Barlow, 2011; Barlow et al.,
2011; Kerosky et al,. 2012; Smultea et al., 2013; [Scaron]irovi[cacute]
et al., 2015), (2) examples of documented presence and site fidelity of
species and long-term residence by individual animals of some species
(Hooker et al.,
[[Page 10015]]
2002; McSweeney et al., 2007; McSweeney et al., 2010; Martin and Kok,
2011; Baumann-Pickering et al., 2012; Falcone and Schorr, 2014), (3)
use of training and testing areas for breeding and nursing activities
(Littnan, 2010), and (4) 6 years of comprehensive monitoring data
indicating a lack of any observable effects to marine mammal
populations as a result of Navy training and testing activities.
To summarize, while the evidence covers most marine mammal
taxonomic suborders, it is limited to a few species and only suggestive
of the general viability of those species in intensively used Navy
training and testing areas (Barlow et al., 2011; Calambokidis et al.,
2009b; Falcone et al., 2009; Littnan, 2011; Martin and Kok, 2011;
McCarthy et al., 2011; McSweeney et al., 2007; McSweeney et al., 2009;
Moore and Barlow, 2011; Tyack et al., 2011; Southall et al., 2012a;
Melcon, 2012; Goldbogen, 2013; Baird et al., 2013). However, there is
no direct evidence that routine Navy training and testing spanning
decades has negatively impacted marine mammal populations at any Navy
Range Complex. Although there have been a few strandings associated
with use of sonar in other locations (see U.S. Department of the Navy,
2013b), Ketten (2012) has recently summarized, ``to date, there has
been no demonstrable evidence of acute, traumatic, disruptive, or
profound auditory damage in any marine mammal as the result of
anthropogenic noise exposures, including sonar.'' Therefore, based on
the best available science (Barlow et al., 2011; Carretta et al., 2011;
Falcone et al., 2009; Falcone and Schorr, 2012, 2014; Jeffries et al.,
2003; Littnan, 2011; Martin and Kok, 2011; McCarthy et al., 2011;
McSweeney et al., 2007; McSweeney et al., 2009; Moore and Barlow, 2011;
Tyack et al., 2011; Southall et al., 2012, 2013, 2014; Manzano-Roth et
al., 2013; DeRuiter et al., 2013b; Goldbogen et al., 2013; Moretti et
al., 2014; Smultea and Jefferson, 2014; [Scaron]irovi[cacute] et al.
2015), including data developed in the series of 80+ reports submitted
to NMFS, we believe that long-term consequences for individuals or
populations are unlikely to result from Navy training activities in the
Study Area.
Preliminary Determination
Training activities proposed in the GOA TMAA Study Area would
result in mainly Level B and some Level A takes, as summarized in
Tables 12 and 13. Based on best available science, NMFS concludes that
exposures to marine mammal species and stocks due to GOA TMAA
activities would result in individuals experiencing primarily short-
term (temporary and short in duration) and relatively infrequent
effects of the type or severity not expected to be additive. In
addition, only a generally small portion of the stocks and species is
likely to be exposed.
Marine mammal takes from Navy activities are not expected to impact
annual rates of recruitment or survival and will therefore not result
in population-level impacts for the following reasons:
Most acoustic exposures (greater than 99 percent) would be
within the non-injurious TTS or behavioral effects zones (Level B
harassment consisting of generally temporary modifications in behavior)
and none of the estimated exposures would result in mortality.
As mentioned earlier, an animal's exposure to a higher
received level is more likely to result in a behavioral response that
is more likely to adversely affect the health of the animal. For low
frequency cetaceans (mysticetes) in the Study Area, most Level B
exposures will occur at received levels less than 156 dB. The majority
of estimated odontocete takes from MFAS/HFAS (at least for hull-mounted
sonar, which is responsible for most of the sonar-related takes) also
result from exposures to received levels less than 156 dB. Therefore,
the majority of Level B takes are expected to be in the form of milder
responses (i.e., lower-level exposures that still rise to the level of
a take, but would likely be in the less severe range of responses that
qualify as a take), and are not expected to have deleterious impacts on
the fitness of any individuals. Marine mammal densities inputted into
the acoustic effects model are also conservative, particularly when
considering species for which data in portions of the Study Area is
limited, and when considering the seasonal migrations that extend
throughout the Study Area.
Acoustic disturbances caused by Navy sonar and explosives
are short-term, intermittent, and (in the case of sonar) transitory.
Even when an animal's exposure to active sonar may be more than one
time, the intermittent nature of the sonar signal, the signal's low
duty cycle (MFAS has a typical ping of every 50 seconds), and the fact
that both the vessel and animal are moving, provide a very small chance
that exposure to active sonar for individual animals and stocks would
be repeated over extended periods of time. Consequently, we would not
expect the Navy's activities to create conditions of long-term,
continuous underwater noise leading to habitat abandonment or long-term
hormonal or physiological stress responses in marine mammals.
Range complexes where intensive training and testing have
been occurring for decades have populations of multiple species with
strong site fidelity (including highly sensitive resident beaked whales
at some locations) and increases in the number of some species.
Populations of beaked whales and other odontocetes in the Bahamas, and
in other Navy fixed ranges that have been operating for tens of years,
appear to be stable.
Navy monitoring of Navy-wide activities since 2006 has
documented hundreds of thousands of marine mammals on the range
complexes and there are only two instances of overt behavioral change
that have been observed.
Navy monitoring of Navy-wide activities since 2006 has
documented no demonstrable instances of injury to marine mammals as a
result of non-impulsive acoustic sources.
In at least three decades of similar Navy activities, only
one instance of injury to marine mammals (March 25, 2011; three long-
beaked common dolphin off Southern California) has occurred as a known
result of training or testing using an impulsive source (underwater
explosion). Of note, the time-delay firing underwater explosive
training activity implicated in the March 4 incident is not proposed
for the training activities in the GOA Study Area.
The protective measures described in the Proposed
Mitigation section above are designed to reduce vessel strike potential
and avoid sound exposures that may cause serious injury, and to result
in the least practicable adverse effect on marine mammal species or
stocks.
Based on this analysis of the likely effects of the specified
activity on marine mammals and their habitat, which includes
consideration of the materials provided in the Navy's LOA application
and GOA DSEIS/OEIS, and dependent upon the implementation of the
mitigation and monitoring measures, NMFS finds that the total marine
mammal take from the Navy's training and testing activities in the GOA
Study Area will have a negligible impact on the affected marine mammal
species or stocks. NMFS proposes to issue regulations for these
activities in order to prescribe the means of effecting the least
practicable adverse impact on marine mammal species or stocks and their
habitat, and to set forth requirements pertaining to the monitoring and
reporting of that taking.
[[Page 10016]]
Subsistence Harvest of Marine Mammals
There are no relevant subsistence uses of marine mammals implicated
by this action. None of the proposed training activities in the Study
Area occur where traditional Arctic subsistence hunting exists.
Therefore, NMFS has preliminarily determined that the total taking
affecting species or stocks would not have an unmitigable adverse
impact on the availability of such species or stocks for taking for
subsistence purposes.
ESA
There are eight marine mammal species under NMFS jurisdiction that
are listed as endangered or threatened under the ESA with confirmed or
possible occurrence in the Study Area: Blue whale, fin whale, humpback
whale, sei whale, sperm whale, gray whale (Western North Pacific
stock), North Pacific right whale, and Steller sea lion (Western U.S.
stock). The Navy will consult with NMFS pursuant to section 7 of the
ESA, and NMFS will also consult internally on the issuance of a LOA
under section 101(a)(5)(A) of the MMPA for GOA TMAA activities.
Consultation will be concluded prior to a determination on the issuance
of the final rule and a LOA.
NEPA
NMFS is a cooperating agency on the Navy's GOA DSEIS/OEIS, which
was prepared and released to the public August 23, 2014. Upon
completion, the GOA Final SEIS/OEIS will be made available for public
review and posted on NMFS' Web site: https://www.nmfs.noaa.gov/pr/permits/incidental/military.htm. NMFS intends to adopt the GOA Final
SEIS/OEIS, if adequate and appropriate. Currently, we believe that the
adoption of the GOA Final SEIS/OEIS will allow NMFS to meet its
responsibilities under NEPA for the issuance of regulations and LOA for
GOA TMAA. If the GOA SEIS/OEIS is deemed inadequate by NMFS, NMFS would
supplement the existing analysis to ensure that we comply with NEPA
prior to issuing the final rule and LOA.
Classification
The Office of Management and Budget has determined that this
proposed rule is not significant for purposes of Executive Order 12866.
Pursuant to the Regulatory Flexibility Act (RFA), the Chief Counsel
for Regulation of the Department of Commerce has certified to the Chief
Counsel for Advocacy of the Small Business Administration that this
proposed rule, if adopted, would not have a significant economic impact
on a substantial number of small entities. The RFA requires federal
agencies to prepare an analysis of a rule's impact on small entities
whenever the agency is required to publish a notice of proposed
rulemaking. However, a federal agency may certify, pursuant to 5 U.S.C.
605 (b), that the action will not have a significant economic impact on
a substantial number of small entities. The Navy is the sole entity
that would be affected by this rulemaking, and the Navy is not a small
governmental jurisdiction, small organization, or small business, as
defined by the RFA. Any requirements imposed by an LOA issued pursuant
to these regulations, and any monitoring or reporting requirements
imposed by these regulations, would be applicable only to the Navy.
NMFS does not expect the issuance of these regulations or the
associated LOA to result in any impacts to small entities pursuant to
the RFA. Because this action, if adopted, would directly affect the
Navy and not a small entity, NMFS concludes the action would not result
in a significant economic impact on a substantial number of small
entities.
List of Subjects in 50 CFR Part 218
Exports, Fish, Imports, Incidental take, Indians, Labeling, Marine
mammals, Navy, Penalties, Reporting and recordkeeping requirements,
Seafood, Sonar, Transportation.
Dated: February 17, 2016.
Samuel D. Rauch III,
Deputy Assistant Administrator for Regulatory Programs, National Marine
Fisheries Service.
For reasons set forth in the preamble, 50 CFR part 218 is proposed
to be amended as follows:
PART 218--REGULATIONS GOVERNING THE TAKING AND IMPORTING OF MARINE
MAMMALS
0
1. The authority citation for part 218 continues to read as follows:
Authority: 16 U.S.C. 1361 et seq.
Subpart N--[Removed and Reserved]
0
3. Remove and reserve subpart N, consisting of Sec. Sec. 218.120
through 218.129.
0
4. Subpart P is added to part 218 to read as follows:
Subpart P--Taking and Importing Marine Mammals; U.S. Navy's Gulf of
Alaska Temporary Maritime Activities Area (GOA TMAA) Study Area
Sec.
218.150 Specified activity and specified geographical region.
218.151 Effective dates.
218.152 Permissible methods of taking.
218.153 Prohibitions.
218.154 Mitigation.
218.155 Requirements for monitoring and reporting.
218.156 Applications for letters of authorization.
218.157 Letters of authorization.
218.158 Renewal and modifications of letters of authorization and
adaptive management.
Subpart P--Taking and Importing Marine Mammals; U.S. Navy's Gulf of
Alaska Temporary Maritime Activities Area (GOA TMAA) Study Area
Sec. 218.150 Specified activity and specified geographical region.
(a) Regulations in this subpart apply only to the U.S. Navy for the
taking of marine mammals that occurs in the area outlined in paragraph
(b) of this section and that occurs incidental to the activities
described in paragraph (c) of this section.
(b) The taking of marine mammals by the Navy is only authorized if
it occurs within the GOA TMAA Study Area, which is bounded by a hexagon
with the following six corners: 57[deg]30'[deg] N. lat.,
141[deg]30'[deg] W. long.; 59[deg]36'[deg] N. lat., 148[deg]10'[deg] W.
long.; 58[deg]57'[deg] N. lat., 150[deg]04'[deg] W. long.;
58[deg]20'[deg] N. lat., 151[deg]00'[deg] W. long.; 57[deg]16'[deg] N.
lat., 151[deg]00'[deg] W. long.; and 55[deg]30'[deg] N. lat.,
142[deg]00'[deg] W. long.
(c) The taking of marine mammals by the Navy is only authorized if
it occurs incidental to the following activities:
(1) Sonar and other Active Sources Used During Training:
(i) Mid-frequency (MF) Source Classes:
(A) MF1--an average of 541 hours per year.
(B) MF3--an average of 48 hours per year.
(C) MF4--an average of 53 hours per year.
(D) MF5--an average of 25 items per year.
(E) MF6--an average of 21 items per year.
(F) MF11--an average of 78 hours per year.
(ii) High-frequency (HF) Source Classes:
(A) HF1--an average of 24 hours per year.
(B) HF6--an average of 80 items per year.
(iii) Anti-Submarine Warfare (ASW) Source Classes:
(A) ASW2--an average of 80 hours per year.
(B) ASW3--an average of 546 hours per year.
(C) ASW4--an average 4 items per year.
[[Page 10017]]
(iv) Torpedoes (TORP):
(A) TORP2--an average of 5 items per year.
(B) [Reserved]
(2) Impulsive Source Detonations During Training:
(i) Explosive Classes:
(A) E5 (>5 to 10 pound [lb] net explosive weight (NEW))--an average
of 112 detonations per year.
(B) E6 (>10 to 20 lb NEW)--an average of 2 detonations per year.
(C) E7 (>20 to 60 lb NEW)--an average of 4 detonations per year.
(D) E8 (>60 to 100 lb NEW)--an average of 6 detonations per year.
(E) E9 (>100 to 250 lb NEW)--an average of 142 detonations per
year.
(F) E10 (>250 to 500 lb NEW)--an average of 32 detonations per
year.
(G) E11 (>500 to 650 lb NEW)--an average of 2 detonations per year.
(H) E12 (>650 to 1,000 lb NEW)--an average of 4 detonations per
year.
(ii) [Reserved]
Sec. 218.151 Effective dates.
Regulations in this subpart are effective May 4, 2016, through May
3, 2021.
Sec. 218.152 Permissible methods of taking.
(a) Under letter of authorization (LOA) issued pursuant to
Sec. Sec. 216.106 and 218.157 of this chapter, the holder of the LOA
may incidentally, but not intentionally, take marine mammals within the
area described in Sec. 218.150, provided the activity is in compliance
with all terms, conditions, and requirements of these regulations and
the LOA.
(b) The activities identified in Sec. 218.150(c) must be conducted
in a manner that minimizes, to the greatest extent practicable, any
adverse impacts on marine mammals and their habitat.
(c) The incidental take of marine mammals under the activities
identified in Sec. 218.150(c) is limited to the following species, by
the identified method of take and the indicated number of times:
(1) Level B Harassment for all Training Activities:
(i) Mysticetes:
(A) Blue whale (Balaenoptera musculus), Eastern North Pacific--475
(an average of 95 per year).
(B) Fin whale (Balaenoptera physalus), Northeast Pacific--12,910
(an average of 2,582 per year).
(C) Humpback whale (Megaptera novaeangliae), Central North
Pacific--645 (an average of 129 per year).
(D) Humpback whale (Megaptera novaeangliae), Western North
Pacific--50 (an average of 10 per year).
(E) Minke whale (Balaenoptera acutorostrata), Alaska--435 (an
average of 87 per year).
(F) North Pacific right whale (Eubalaena japonica), Eastern North
Pacific--35 (an average of 7 per year).
(G) Sei whale (Balaenoptera borealis), Eastern North Pacific--65
(an average of 13 per year).
(ii) Odontocetes:
(A) Baird's beaked whale (Berardius bairdii), Alaska--2,005 (an
average of 401 per year).
(B) Cuvier's beaked whale (Ziphius cavirostris), Alaska--12,720 (an
average of 2,544 per year).
(C) Dall's porpoise (Phocoenoidea dalli), Alaska--81,220 (an
average of 16,244 per year).
(D) Harbor porpoise (Phocoena phocoena), GOA--27,420 (an average of
5,484 per year).
(E) Harbor porpoise (Phocoena phocoena), Southeast Alaska--9,630
(an average of 1,926 per year).
(F) Killer whale (Orcinus orca), Alaska Resident--2,820 (an average
of 564 per year).
(G) Killer whale (Orcinus orca), Eastern North Pacific Offshore--
265 (an average of 53 per year).
(H) Killer whale (Orcinus orca), AT1 Transient--5 (an average of 1
per year).
(I) Killer whale (Orcinus orca), GOA, Aleutian Island, and Bearing
Sea Transient--720 (an average of 144 per year).
(J) Pacific white-sided dolphin (Lagenorhynchus obliquidens), North
Pacific--9,815 (an average of 1,963 per year).
(K) Stejneger's beaked whale (Mesoplodon stejnegeri), Alaska--5,765
(an average of 1,153 per year).
(L) Sperm whale (Physeter macrocephalus), North Pacific--985 (an
average of 197 per year).
(iii) Pinnipeds:
(A) California sea lion (Zalophus californianus), U.S.--25 (an
average of 5 per year).
(B) Steller sea lion (Eumetopias jubatus), Eastern U.S.--3,355 (an
average of 671 per year).
(C) Steller sea lion (Eumetopias jubatus), Western U.S.--2,860 (an
average of 572 per year).
(D) Harbor seal (Phoca vitulina), North Kodiak--5 (an average of 1
per year).
(E) Harbor seal (Phoca vitulina), South Kodiak--5 (an average of 1
per year).
(F) Harbor seal (Phoca vitulina), Prince William Sound--10 (an
average of 2 per year).
(G) Northern elephant seal (Mirounga angustirostris), California
Breeding--1,225 (an average of 245 per year).
(H) Northern fur seal (Callorhinus ursinus), Eastern Pacific--7,140
(an average of 1,428 per year).
(2) Level A Harassment for all Training Activities:
(i) Odontocetes:
(A) Dall's porpoise (Phocoenoidea dalli), Alaska--25 (an average of
5 per year).
(B) [Reserved]
(ii) [Reserved]
Sec. 218.153 Prohibitions.
Notwithstanding takings contemplated in Sec. 218.152 and
authorized by an LOA issued under Sec. Sec. 216.106 and 218.157 of
this chapter, no person in connection with the activities described in
Sec. 218.150 may:
(a) Take any marine mammal not specified in Sec. 218.152(c);
(b) Take any marine mammal specified in Sec. 218.152(c) other than
by incidental take as specified in Sec. 218.152(c);
(c) Take a marine mammal specified in Sec. 218.152(c) if such
taking results in more than a negligible impact on the species or
stocks of such marine mammal; or
(d) Violate, or fail to comply with, the terms, conditions, and
requirements of these regulations or an LOA issued under Sec. Sec.
216.106 and 218.157 of this chapter.
Sec. 218.154 Mitigation.
(a) When conducting training activities, as identified in Sec.
218.150, the mitigation measures contained in the LOA issued under
Sec. Sec. 216.106 and 218.157 of this chapter must be implemented.
These mitigation measures include, but are not limited to:
(1) Lookouts.The Navy shall have two types of lookouts for the
purposes of conducting visual observations: Those positioned on ships;
and those positioned ashore, in aircraft, or on boats. The following
are protective measures concerning the use of lookouts.
(i) Lookouts positioned on surface ships shall be dedicated solely
to diligent observation of the air and surface of the water. Their
observation objectives shall include, but are not limited to, detecting
the presence of biological resources and recreational or fishing boats,
observing mitigation zones, and monitoring for vessel and personnel
safety concerns.
(ii) Due to manning and space restrictions on aircraft, small
boats, and some Navy ships, lookouts for these platforms may be
supplemented by the aircraft crew or pilot, boat crew, range site
personnel, or shore-side personnel. Lookouts positioned in minimally
[[Page 10018]]
manned platforms may be responsible for tasks in addition to observing
the air or surface of the water (e.g., navigation of a helicopter or
small boat). However, all lookouts shall, considering personnel safety,
practicality of implementation, and impact on the effectiveness of the
activity, comply with the observation objectives described above for
lookouts positioned on ships.
(iii) All personnel standing watch on the bridge, Commanding
Officers, Executive Officers, maritime patrol aircraft aircrews, anti-
submarine warfare helicopter crews, civilian equivalents, and lookouts
shall successfully complete the United States Navy Marine Species
Awareness Training prior to standing watch or serving as a lookout.
(iv) Lookout measures for non-impulsive sound:
(A) With the exception of vessels less than 65 ft (20 m) in length,
ships using hull-mounted mid-frequency active sonar sources associated
with anti-submarine warfare activities at sea shall have two Lookouts
at the forward position of the vessel.
(B) While using hull-mounted mid-frequency active sonar sources
associated with anti-submarine warfare activities at sea, vessels less
than 65 ft (20 m) in length shall have one lookout at the forward
position of the vessel due to space and manning restrictions.
(C) During non-hull mounted mid-frequency active sonar training
activities, Navy aircraft participating in exercises at sea shall
conduct and maintain, when operationally feasible and safe,
surveillance for marine species of concern as long as it does not
violate safety constraints or interfere with the accomplishment of
primary operational duties. Helicopters shall observe/survey the
vicinity of an anti-submarine warfare training event for 10 minutes
before the first deployment of active (dipping) sonar in the water.
(D) Ships or aircraft conducting non-hull-mounted mid-frequency
active sonar, such as helicopter dipping sonar systems, shall maintain
one lookout.
(E) Ships conducting high-frequency active sonar shall maintain one
lookout.
(v) Lookout measures for explosives and impulsive sound:
(A) Aircraft conducting explosive signal underwater sound buoy
activities using >0.5-2.5 lb. NEW shall have one lookout.
(B) Surface vessels or aircraft conducting small-, medium-, or
large-caliber gunnery exercises against a surface target shall have one
lookout. From the intended firing position, trained lookouts shall
survey the mitigation zone for marine mammals prior to commencement and
during the exercise as long as practicable. Towing vessels, if
applicable, shall also maintain one lookout. If a marine mammal is
sighted in the vicinity of the exercise, the tow vessel shall
immediately notify the firing vessel in order to secure gunnery firing
until the area is clear.
(C) Aircraft conducting explosive bombing exercises shall have one
lookout and any surface vessels involved shall have trained Lookouts.
If surface vessels are involved, lookouts shall survey for floating
kelp and marine mammals. Aircraft shall visually survey the target and
buffer zone for marine mammals prior to and during the exercise. The
survey of the impact area shall be made by flying at 1,500 ft. (460 m)
or lower, if safe to do so, and at the slowest safe speed. Release of
ordnance through cloud cover is prohibited: Aircraft must be able to
actually see ordnance impact areas. Survey aircraft should employ most
effective search tactics and capabilities.
(D) When aircraft are conducting missile exercises against a
surface target, the Navy shall have one Lookout positioned in an
aircraft. Aircraft shall visually survey the target area for marine
mammals. Visual inspection of the target area shall be made by flying
at 1,500 ft. (457 m) or lower, if safe to do so, and at slowest safe
speed. Firing or range clearance aircraft must be able to actually see
ordnance impact areas.
(E) Ships conducting explosive and non-explosive gunnery exercises
shall have one Lookout on the ship. This may be the same lookout
described in paragraph (B) above for surface vessels conducting small-,
medium-, or large-caliber gunnery exercises when that activity is
conducted from a ship against a surface target.
(F) During sinking exercises, two Lookouts shall be used. One
lookout shall be positioned in an aircraft and one lookout shall be
positioned on a vessel.
(vi) Lookout measures for physical strike and disturbance:
(A) While underway, surface ships shall have at least one lookout.
(B) [Reserved]
(vii) Lookout measures for non-explosive practice munitions:
(A) Gunnery exercises using non-explosive practice munitions (e.g.,
small-, medium-, and large-caliber) using a surface target shall have
one lookout.
(B) During non-explosive bombing exercises one lookout shall be
positioned in an aircraft and trained lookouts shall be positioned in
any surface vessels involved.
(C) When aircraft are conducting non-explosive missile exercises
(including exercises using rockets) against a surface target, the Navy
shall have one lookout positioned in an aircraft.
(2) Mitigation Zones--The following are protective measures
concerning the implementation of mitigation zones.
(i) Mitigation zones shall be measured as the radius from a source
and represent a distance to be monitored.
(ii) Visual detections of marine mammals or sea turtles within a
mitigation zone shall be communicated immediately to a watch station
for information dissemination and appropriate action.
(iii) Mitigation zones for non-impulsive sound:
(A) The Navy shall ensure that hull-mounted mid-frequency active
sonar transmission levels are limited to at least 6 dB below normal
operating levels if any detected marine mammals or sea turtles are
within 1,000 yd. (914 m) of the sonar dome (the bow).
(B) The Navy shall ensure that hull-mounted mid-frequency active
sonar transmissions are limited to at least 10 dB below the equipment's
normal operating level if any detected marine mammals or sea turtles
are within 500 yd. (457 m) of the sonar dome.
(C) The Navy shall ensure that hull-mounted mid-frequency active
sonar transmissions are ceased if any detected cetaceans or sea turtles
are within 200 yd. (183 m) and pinnipeds are within 100 yd. (90 m) of
the sonar dome. Transmissions shall not resume until the marine mammal
has been observed exiting the mitigation zone, is thought to have
exited the mitigation zone based on its course and speed, has not been
detected for 30 minutes, the vessel has transited more than 2,000 yd.
beyond the location of the last detection, or the ship concludes that
dolphins are deliberately closing in on the ship to ride the ship's bow
wave (and there are no other marine mammal sightings within the
mitigation zone). Active transmission may resume when dolphins are bow
riding because they are out of the main transmission axis of the active
sonar while in the shallow-wave area of the ship bow.
(D) The Navy shall ensure that high-frequency and non-hull-mounted
mid-frequency active sonar transmission levels are ceased if any
detected cetaceans are within 200 yd. (180 m) and pinnipeds are within
100 yd. (90 m) of the source. Transmissions shall not resume until the
marine mammal has been observed exiting the mitigation zone, is thought
to have exited the mitigation zone based on its course and speed, the
mitigation zone has been
[[Page 10019]]
clear from any additional sightings for a period of 10 minutes for an
aircraft-deployed source, the mitigation zone has been clear from any
additional sightings for a period of 30 minutes for a vessel-deployed
source, the vessel or aircraft has repositioned itself more than 400
yd. (370 m) away from the location of the last sighting, or the vessel
concludes that dolphins are deliberately closing in to ride the
vessel's bow wave (and there are no other marine mammal sightings
within the mitigation zone).
(iv) Mitigation zones for explosive and impulsive sound:
(A) A mitigation zone with a radius of 350 yd. (320 m) shall be
established for explosive signal underwater sonobuoys using >0.5 to 2.5
lb NEW. Explosive signal underwater sonobuoys shall not be deployed if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone (around the intended deployment location).
Explosive signal underwater sonobuoy deployment shall cease if a marine
mammal is sighted within the mitigation zone. Detonations shall
recommence if any one of the following conditions is met: The animal is
observed exiting the mitigation zone, the animal is thought to have
exited the mitigation zone based on its course and speed, or the
mitigation zone has been clear from any additional sightings for a
period of 10 minutes. Passive acoustic monitoring shall also be
conducted with Navy assets, such as sonobuoys, already participating in
the activity. These assets would only detect vocalizing marine mammals
within the frequency bands monitored by Navy personnel. Passive
acoustic detections would not provide range or bearing to detected
animals, and therefore cannot provide locations of these animals.
Passive acoustic detections would be reported to Lookouts posted in
aircraft in order to increase vigilance of their visual surveillance.
(B) A mitigation zone with a radius of 200 yd. (180 m) shall be
established for small- and medium-caliber gunnery exercises with a
surface target. The exercise shall not commence if concentrations of
floating vegetation (kelp paddies) are observed in the mitigation zone.
Firing shall cease if a marine mammal is sighted within the mitigation
zone. Firing shall recommence if any one of the following conditions is
met: The animal is observed exiting the mitigation zone, the animal is
thought to have exited the mitigation zone based on its course and
speed, the mitigation zone has been clear from any additional sightings
for a period of 10 minutes for a firing aircraft, the mitigation zone
has been clear from any additional sightings for a period of 30 minutes
for a firing ship, or the intended target location has been
repositioned more than 400 yd. (370 m) away from the location of the
last sighting.
(C) A mitigation zone with a radius of 600 yd. (549 m) shall be
established for large-caliber gunnery exercises with a surface target.
The exercise shall not commence if concentrations of floating
vegetation (kelp paddies) are observed in the mitigation zone. Firing
shall cease if a marine mammal is sighted within the mitigation zone.
Firing shall recommence if any one of the following conditions is met:
The animal is observed exiting the mitigation zone, the animal is
thought to have exited the mitigation zone based on its course and
speed, or the mitigation zone has been clear from any additional
sightings for a period of 30 minutes.
(D) A mitigation zone with a radius of 900 yd. (823 m) shall be
established for missile exercises with up to 250 lb NEW and a surface
target. The exercise shall not commence if concentrations of floating
vegetation (kelp paddies) are observed in the mitigation zone. Firing
shall cease if a marine mammal is sighted within the mitigation zone.
Firing shall recommence if any one of the following conditions is met:
The animal is observed exiting the mitigation zone, the animal is
thought to have exited the mitigation zone based on its course and
speed, or the mitigation zone has been clear from any additional
sightings for a period of 10 minutes or 30 minutes (depending on
aircraft type).
(E) A mitigation zone with a radius of 2,000 yd. (1.8 km) shall be
established for missile exercises with 251 to 500 lb NEW using a
surface target. The exercise shall not commence if concentrations of
floating vegetation (kelp paddies) are observed in the mitigation zone.
Firing shall cease if a marine mammal is sighted within the mitigation
zone. Firing shall recommence if any one of the following conditions is
met: The animal is observed exiting the mitigation zone, the animal is
thought to have exited the mitigation zone based on its course and
speed, or the mitigation zone has been clear from any additional
sightings for a period of 10 minutes or 30 minutes (depending on
aircraft type).
(F) A mitigation zone with a radius of 2,500 yd. (2.3 km) around
the intended impact location for explosive bombs and 1000 yd. (920 m)
for non-explosive bombs shall be established for bombing exercises. The
exercise shall not commence if concentrations of floating vegetation
(kelp paddies) are observed in the mitigation zone. Bombing shall cease
if a marine mammal is sighted within the mitigation zone. Bombing shall
recommence if any one of the following conditions is met: The animal is
observed exiting the mitigation zone, the animal is thought to have
exited the mitigation zone based on its course and speed, or the
mitigation zone has been clear from any additional sightings for a
period of 10 minutes.
(G) A mitigation zone with a radius of 2.5 nautical miles shall be
established for sinking exercises. Sinking exercises shall include
aerial observation beginning 90 minutes before the first firing, visual
observations from vessels throughout the duration of the exercise, and
both aerial and vessel observation immediately after any planned or
unplanned breaks in weapons firing of longer than 2 hours. Prior to
conducting the exercise, the Navy shall review remotely sensed sea
surface temperature and sea surface height maps to aid in deciding
where to release the target ship hulk. The Navy shall also monitor
using passive acoustics during the exercise. Passive acoustic
monitoring would be conducted with Navy assets, such as passive ships
sonar systems or sonobuoys, already participating in the activity.
These assets would only detect vocalizing marine mammals within the
frequency bands monitored by Navy personnel. Passive acoustic
detections would not provide range or bearing to detected animals, and
therefore cannot provide locations of these animals. Passive acoustic
detections would be reported to lookouts posted in aircraft and on
vessels in order to increase vigilance of their visual surveillance.
Lookouts shall also increase observation vigilance before the use of
torpedoes or unguided ordnance with a NEW of 500 lb. or greater, or if
the Beaufort sea state is a 4 or above. The exercise shall not commence
if concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone. The exercise shall cease if a marine mammal, sea
turtle, or aggregation of jellyfish is sighted within the mitigation
zone. The exercise shall recommence if any one of the following
conditions is met: The animal is observed exiting the mitigation zone,
the animal is thought to have exited the mitigation zone based on a
determination of its course and speed and the relative motion between
the animal and the source, or the mitigation zone has been clear from
any additional sightings for a period of 30 minutes. Upon sinking the
vessel, the Navy shall conduct post-exercise visual surveillance of the
mitigation zone for 2
[[Page 10020]]
hours (or until sunset, whichever comes first).
(H) A mitigation zone of 70 yd. (46 m) shall be established for all
explosive large-caliber gunnery exercises conducted from a ship. The
exercise shall not commence if concentrations of floating vegetation
(kelp paddies) are observed in the mitigation zone. Firing shall cease
if a marine mammal is sighted within the mitigation zone. Firing shall
recommence if any one of the following conditions is met: The animal is
observed exiting the mitigation zone, the animal is thought to have
exited the mitigation zone based on its course and speed, the
mitigation zone has been clear from any additional sightings for a
period of 30 minutes, or the vessel has repositioned itself more than
140 yd. (128 m) away from the location of the last sighting.
(v) Mitigation zones for vessels and in-water devices:
(A) A mitigation zone of 500 yd. (460 m) for observed whales and
200 yd (183 m) for all other marine mammals (except bow riding
dolphins) shall be established for all vessel movement during training
activities, providing it is safe to do so.
(B) A mitigation zone of 250 yd. (229 m) shall be established for
all towed in-water devices, providing it is safe to do so.
(vi) Mitigation zones for non-explosive practice munitions:
(A) A mitigation zone of 200 yd. (180 m) shall be established for
small, medium, and large caliber gunnery exercises using a surface
target. The exercise shall not commence if concentrations of floating
vegetation (kelp paddies) are observed in the mitigation zone. Firing
shall cease if a marine mammal is sighted within the mitigation zone.
Firing shall recommence if any one of the following conditions is met:
The animal is observed exiting the mitigation zone, the animal is
thought to have exited the mitigation zone based on its course and
speed, the mitigation zone has been clear from any additional sightings
for a period of 10 minutes for a firing aircraft, the mitigation zone
has been clear from any additional sightings for a period of 30 minutes
for a firing ship, or the intended target location has been
repositioned more than 400 yd. (370 m) away from the location of the
last sighting.
(B) A mitigation zone of 1,000 yd. (920 m) shall be established for
bombing exercises. Bombing shall cease if a marine mammal is sighted
within the mitigation zone. The exercise shall not commence if
concentrations of floating vegetation (kelp paddies) are observed in
the mitigation zone. Bombing shall recommence if any one of the
following conditions is met: The animal is observed exiting the
mitigation zone, the animal is thought to have exited the mitigation
zone based on its course and speed, or the mitigation zone has been
clear from any additional sightings for a period of 10 minutes.
(C) A mitigation zone of 900 yd. (823 m) shall be established for
missile exercises (including rockets) using a surface target. The
exercise shall not commence if concentrations of floating vegetation
(kelp paddies) are observed in the mitigation zone. Firing shall cease
if a marine mammal is sighted within the mitigation zone. Firing shall
recommence if any one of the following conditions is met: The animal is
observed exiting the mitigation zone, the animal is thought to have
exited the mitigation zone based on its course and speed, or the
mitigation zone has been clear from any additional sightings for a
period of 10 minutes or 30 minutes (depending on aircraft type).
(3) Stranding response plan. (i) The Navy shall abide by the letter
of the ``Stranding Response Plan for Major Navy Training Exercises in
the GOA TMAA Study Area,'' to include the following measures:
(A) Shutdown procedures. When an Uncommon Stranding Event (USE)
occurs during a Major Training Exercise (MTE) in the Study Area, the
Navy shall implement the procedures described below:
(1) The Navy shall implement a shutdown when advised by a NMFS
Office of Protected Resources Headquarters Senior Official designated
in the GOA TMAA Study Area Stranding Communication Protocol that a USE
involving live animals has been identified and that at least one live
animal is located in the water. NMFS and the Navy shall maintain a
dialogue, as needed, regarding the identification of the USE and the
potential need to implement shutdown procedures.
(2) Any shutdown in a given area shall remain in effect in that
area until NMFS advises the Navy that the subject(s) of the USE at that
area die or are euthanized, or that all live animals involved in the
USE at that area have left the area (either of their own volition or
herded).
(3) If the Navy finds an injured or dead animal floating at sea
during an MTE, the Navy shall notify NMFS immediately or as soon as
operational security considerations allow. The Navy shall provide NMFS
with species or description of the animal(s), the condition of the
animal(s), including carcass condition if the animal(s) is/are dead,
location, time of first discovery, observed behavior (if alive), and
photo or video (if available). Based on the information provided, NFMS
shall determine if, and advise the Navy whether a modified shutdown is
appropriate on a case-by-case basis.
(4) In the event, following a USE, that qualified individuals are
attempting to herd animals back out to the open ocean and animals are
not willing to leave, or animals are seen repeatedly heading for the
open ocean but turning back to shore, NMFS and the Navy shall
coordinate (including an investigation of other potential anthropogenic
stressors in the area) to determine if the proximity of mid-frequency
active sonar training activities or explosive detonations, though
farther than 14 nautical miles from the distressed animal(s), is likely
contributing to the animals' refusal to return to the open water. If
so, NMFS and the Navy shall further coordinate to determine what
measures are necessary to improve the probability that the animals will
return to open water and implement those measures as appropriate.
(B) Within 72 hours of NMFS notifying the Navy of the presence of a
USE, the Navy shall provide available information to NMFS (per the GOA
TMAA Study Area Communication Protocol) regarding the location, number
and types of acoustic/explosive sources, direction and speed of units
using mid-frequency active sonar, and marine mammal sightings
information associated with training activities occurring within 80
nautical miles (148 km) and 72 hours prior to the USE event.
Information not initially available regarding the 80-nautical miles
(148-km), 72-hour period prior to the event shall be provided as soon
as it becomes available. The Navy shall provide NMFS investigative
teams with additional relevant unclassified information as requested,
if available.
(ii) [Reserved]
(b) [Reserved]
Sec. 218.155 Requirements for monitoring and reporting.
(a) The Holder of the Authorization must notify NMFS immediately
(or as soon as operational security considerations allow) if the
specified activity identified in Sec. 218.150 is thought to have
resulted in the mortality or injury of any marine mammals, or in any
take of marine mammals not identified in Sec. 218.152(c).
(b) The Holder of the LOA must conduct all monitoring and required
reporting under the LOA, including abiding by the GOA TMAA monitoring
plan.
[[Page 10021]]
(c) General notification of injured or dead marine mammals. Navy
personnel shall ensure that NMFS (regional stranding coordinator) is
notified immediately (or as soon as operational security considerations
allow) if an injured or dead marine mammal is found during or shortly
after, and in the vicinity of, a Navy training activity utilizing mid-
or high-frequency active sonar, or underwater explosive detonations.
The Navy shall provide NMFS with species or description of the
animal(s), the condition of the animal(s) (including carcass condition
if the animal is dead), location, time of first discovery, observed
behaviors (if alive), and photo or video (if available). In the event
that an injured, stranded, or dead marine mammal is found by the Navy
that is not in the vicinity of, or during or shortly after, MFAS, HFAS,
or underwater explosive detonations, the Navy shall report the same
information as listed above as soon as operationally feasible and
clearance procedures allow.
(d) General notification of ship strike. In the event of a ship
strike by any Navy vessel, at any time or place, the Navy shall do the
following:
(1) Immediately report to NMFS the species identification (if
known), location (lat/long) of the animal (or the strike if the animal
has disappeared), and whether the animal is alive or dead (or unknown),
and the time of the strike.
(2) Report to NMFS as soon as operationally feasible the size and
length of animal, an estimate of the injury status (ex., dead, injured
but alive, injured and moving, unknown, etc.), vessel class/type and
operational status.
(3) Report to NMFS the vessel length, speed, and heading as soon as
feasible.
(4) Provide NMFS a photo or video, if equipment is available.
(5) Within 2 weeks of the strike, provide NMFS with a detailed
description of the specific actions of the vessel in the 30-minute
timeframe immediately preceding the strike, during the event, and
immediately after the strike (e.g., the speed and changes in speed, the
direction and changes in direction, other maneuvers, sonar use, etc.,
if not classified); a narrative description of marine mammal sightings
during the event and immediately after, and any information as to
sightings prior to the strike, if available; and use established Navy
shipboard procedures to make a camera available to attempt to capture
photographs following a ship strike.
(e) Communication plan. The Navy and NMFS shall develop a
communication plan that will include all of the communication protocols
(phone trees, etc.) and associated contact information required for
NMFS and the Navy to carry out the necessary expeditious communication
required in the event of a stranding or ship strike, including
information described in the proposed notification measures above.
(f) Annual GOA TMAA monitoring report. The Navy shall submit an
annual report of the GOA TMAA monitoring describing the implementation
and results from the previous calendar year. Data collection methods
shall be standardized across range complexes and study areas to allow
for comparison in different geographic locations. Although additional
information will be gathered, the protected species observers
collecting marine mammal data pursuant to the GOA TMAA monitoring plan
shall, at a minimum, provide the same marine mammal observation data
required in Sec. 218.155. The report shall be submitted either 90 days
after the calendar year, or 90 days after the conclusion of the
monitoring year to be determined by the Adaptive Management process.
The GOA TMAA Monitoring Report may be provided to NMFS within a larger
report that includes the required Monitoring Plan reports from multiple
range complexes and study areas (the multi-Range Complex Annual
Monitoring Report). Such a report would describe progress of knowledge
made with respect to monitoring plan study questions across all Navy
ranges associated with the Integrated Comprehensive Monitoring Program.
Similar study questions shall be treated together so that progress on
each topic shall be summarized across all Navy ranges. The report need
not include analyses and content that does not provide direct
assessment of cumulative progress on the monitoring plan study
questions.
(g) Annual GOA TMAA exercise reports. Each year, the Navy shall
submit a preliminary report detailing the status of authorized sound
sources within 21 days after the anniversary of the date of issuance of
the LOA. Each year, the Navy shall submit a detailed report within 3
months after the anniversary of the date of issuance of the LOA. The
annual report shall contain information on Major Training Exercises
(MTEs), Sinking Exercise (SINKEX) events, and a summary of all sound
sources used, as described in paragraph (g)(3) of this section. The
analysis in the detailed report shall be based on the accumulation of
data from the current year's report and data collected from previous
the report. The detailed reports shall contain information identified
in paragraphs (g)(1) through (4) of this section.
(1) MFAS/HFAS Major Training Exercises--This section shall contain
the following information for Major Training Exercises conducted in the
GOA TMAA:
(i) Exercise Information (for each MTE):
(A) Exercise designator.
(B) Date that exercise began and ended.
(C) Location.
(D) Number and types of active sources used in the exercise.
(E) Number and types of passive acoustic sources used in exercise.
(F) Number and types of vessels, aircraft, etc., participating in
exercise.
(G) Total hours of observation by lookouts.
(H) Total hours of all active sonar source operation.
(I) Total hours of each active sonar source bin.
(J) Wave height (high, low, and average during exercise).
(ii) Individual marine mammal sighting information for each
sighting in each exercise when mitigation occurred:
(A) Date/Time/Location of sighting.
(B) Species (if not possible, indication of whale/dolphin/
pinniped).
(C) Number of individuals.
(D) Initial Detection Sensor.
(E) Indication of specific type of platform observation made from
(including, for example, what type of surface vessel or testing
platform).
(F) Length of time observers maintained visual contact with marine
mammal.
(G) Sea state.
(H) Visibility.
(I) Sound source in use at the time of sighting.
(J) Indication of whether animal is <200 yd, 200 to 500 yd, 500 to
1,000 yd, 1,000 to 2,000 yd, or >2,000 yd from sonar source.
(K) Mitigation implementation. Whether operation of sonar sensor
was delayed, or sonar was powered or shut down, and how long the delay
was.
(L) If source in use is hull-mounted, true bearing of animal from
ship, true direction of ship's travel, and estimation of animal's
motion relative to ship (opening, closing, parallel).
(M) Observed behavior. Lookouts shall report, in plain language and
without trying to categorize in any way, the observed behavior of the
animals (such as animal closing to bow ride, paralleling course/speed,
floating on surface and not swimming, etc.) and if any calves present.
(iii) An evaluation (based on data gathered during all of the MTEs)
of the effectiveness of mitigation measures designed to minimize the
received level
[[Page 10022]]
to which marine mammals may be exposed. This evaluation shall identify
the specific observations that support any conclusions the Navy reaches
about the effectiveness of the mitigation.
(2) SINKEXs. This section shall include the following information
for each SINKEX completed that year:
(i) Exercise information (gathered for each SINKEX):
(A) Location.
(B) Date and time exercise began and ended.
(C) Total hours of observation by lookouts before, during, and
after exercise.
(D) Total number and types of explosive source bins detonated.
(E) Number and types of passive acoustic sources used in exercise.
(F) Total hours of passive acoustic search time.
(G) Number and types of vessels, aircraft, etc., participating in
exercise.
(H) Wave height in feet (high, low, and average during exercise).
(I) Narrative description of sensors and platforms utilized for
marine mammal detection and timeline illustrating how marine mammal
detection was conducted.
(ii) Individual marine mammal observation (by Navy lookouts)
information (gathered for each marine mammal sighting) for each
sighting in each exercise that required mitigation to be implemented:
(A) Date/Time/Location of sighting.
(B) Species (if not possible, indicate whale, dolphin, or
pinniped).
(C) Number of individuals.
(D) Initial detection sensor.
(E) Length of time observers maintained visual contact with marine
mammal.
(F) Sea state.
(G) Visibility.
(H) Whether sighting was before, during, or after detonations/
exercise, and how many minutes before or after.
(I) Distance of marine mammal from actual detonations (or target
spot if not yet detonated).
(J) Observed behavior. Lookouts shall report, in plain language and
without trying to categorize in any way, the observed behavior of the
animal(s) (such as animal closing to bow ride, paralleling course/
speed, floating on surface and not swimming etc.), including speed and
direction and if any calves present.
(K) Resulting mitigation implementation. Indicate whether explosive
detonations were delayed, ceased, modified, or not modified due to
marine mammal presence and for how long.
(L) If observation occurs while explosives are detonating in the
water, indicate munition type in use at time of marine mammal
detection.
(3) Summary of sources used.
(i) This section shall include the following information summarized
from the authorized sound sources used in all training events:
(A) Total annual hours or quantity (per the LOA) of each bin of
sonar or other non-impulsive source;
(B) Total annual number of each type of explosive exercises (of
those identified as part of the ``Specified Activity'' in this proposed
rule) and total annual expended/detonated rounds (missiles, bombs,
sonobuoys, etc.) for each explosive bin.
(4) Geographic information presentation. The reports shall present
an annual (and seasonal, where practical) depiction of training
exercises and testing bin usage geographically across the Study Area.
(g) Sonar exercise notification. The Navy shall submit to NMFS
(contact as specified in the LOA) an electronic report within fifteen
calendar days after the completion of any major training exercise
indicating:
(i) Location of the exercise.
(ii) Beginning and end dates of the exercise.
(iii) Type of exercise.
(h) Five-year close-out exercise report. This report shall be
included as part of the 2021 annual exercise report. This report shall
provide the annual totals for each sound source bin with a comparison
to the annual allowance and the 5-year total for each sound source bin
with a comparison to the 5-year allowance. Additionally, if there were
any changes to the sound source allowance, this report shall include a
discussion of why the change was made and include the analysis to
support how the change did or did not result in a change in the SEIS
and final rule determinations. The report shall be submitted 3 months
after the expiration of this subpart. NMFS shall submit comments on the
draft close-out report, if any, within 3 months of receipt. The report
shall be considered final after the Navy has addressed NMFS' comments,
or 3 months after the submittal of the draft if NMFS does not provide
comments.
Sec. 218.156 Applications for letters of authorization (LOA).
To incidentally take marine mammals pursuant to the regulations in
this subpart, the U.S. citizen (as defined by Sec. 216.106 of this
chapter) conducting the activity identified in Sec. 218.150(c) (the
U.S. Navy) must apply for and obtain either an initial LOA in
accordance with Sec. 218.157 or a renewal under Sec. 218.158.
Sec. 218.157 Letters of authorization (LOA).
(a) An LOA, unless suspended or revoked, shall be valid for a
period of time not to exceed the period of validity of this subpart.
(b) Each LOA shall set forth:
(1) Permissible methods of incidental taking;
(2) Means of effecting the least practicable adverse impact on the
species, its habitat, and on the availability of the species for
subsistence uses (i.e., mitigation); and
(3) Requirements for mitigation, monitoring and reporting.
(c) Issuance and renewal of the LOA shall be based on a
determination that the total number of marine mammals taken by the
activity as a whole shall have no more than a negligible impact on the
affected species or stock of marine mammal(s).
Sec. 218.158 Renewals and modifications of letters of authorization
(LOA) and adaptive management.
(a) A letter of authorization issued under Sec. Sec. 216.106 and
218.157 of this chapter for the activity identified in Sec. 218.150(c)
shall be renewed or modified upon request of the applicant, provided
that:
(1) The proposed specified activity and mitigation, monitoring, and
reporting measures, as well as the anticipated impacts, are the same as
those described and analyzed for these regulations (excluding changes
made pursuant to the adaptive management provision of this chapter),
and;
(2) NMFS determines that the mitigation, monitoring, and reporting
measures required by the previous LOA under these regulations were
implemented.
(b) For LOA modification or renewal requests by the applicant that
include changes to the activity or the mitigation, monitoring, or
reporting (excluding changes made pursuant to the adaptive management
provision of this chapter) that do not change the findings made for the
regulations or result in no more than a minor change in the total
estimated number of takes (or distribution by species or years), NMFS
may publish a notice of proposed LOA in the Federal Register, including
the associated analysis illustrating the change, and solicit public
comment before issuing the LOA.
(c) A LOA issued under Sec. 216.106 and Sec. 218.157 of this
chapter for the activity identified in Sec. 218.154 of this chapter
may be modified by NMFS under the following circumstances:
[[Page 10023]]
(1) Adaptive management. NMFS may modify and augment the existing
mitigation, monitoring, or reporting measures (after consulting with
the Navy regarding the practicability of the modifications) if doing so
creates a reasonable likelihood of more effectively accomplishing the
goals of the mitigation and monitoring.
(i) Possible sources of data that could contribute to the decision
to modify the mitigation, monitoring, and reporting measures in an LOA:
(A) Results from Navy's monitoring from the previous year(s);
(B) Results from other marine mammal and/or sound research or
studies; or
(C) Any information that reveals marine mammals may have been taken
in a manner, extent, or number not authorized by these regulations or
subsequent LOA.
(ii) If, through adaptive management, the modifications to the
mitigation, monitoring, or reporting measures are substantial, NMFS
would publish a notice of proposed LOA in the Federal Register and
solicit public comment.
(2) Emergencies. If NMFS determines that an emergency exists that
poses a significant risk to the well-being of the species or stocks of
marine mammals specified in Sec. 218.152(c), an LOA may be modified
without prior notification and an opportunity for public comment.
Notification would be published in the Federal Register within 30 days
of the action.
[FR Doc. 2016-03622 Filed 2-25-16; 8:45 am]
BILLING CODE 3510-22-P