Takes of Marine Mammals Incidental to Specified Activities; Navy Research, Development, Test and Evaluation Activities at the Naval Surface Warfare Center Panama City Division, 12010-12030 [2012-4695]
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Federal Register / Vol. 77, No. 39 / Tuesday, February 28, 2012 / Notices
Permits and Conservation Division,
Office of Protected Resources, NMFS,
1315 East-West Highway, Room 13705,
Silver Spring, MD 20910; phone (301)
427–8401; fax (301) 713–0376;
Northwest Region, NMFS, 7600 Sand
Point Way NE., BIN C15700, Bldg. 1,
Seattle, WA 98115–0700; phone (206)
526–6150; fax (206) 526–6426;
Alaska Region, NMFS, P.O. Box
21668, Juneau, AK 99802–1668; phone
(907) 586–7221; fax (907) 586–7249; and
Southwest Region, NMFS, 501 West
Ocean Blvd., Suite 4200, Long Beach,
CA 90802–4213; phone (562) 980–4001;
fax (562) 980–4018.
Dated: February 22, 2012.
P. Michael Payne,
Chief, Permits and Conservation Division,
Office of Protected Resources, National
Marine Fisheries Service.
All other previously published
information remains unchanged.
Special Accommodations
The meeting is physically accessible
to people with disabilities. Requests for
sign language interpretation or other
auxiliary aids should be directed to M.
Jan Saunders at the Mid-Atlantic
Council Office (302) 526–5251 at least 5
days prior to the meeting date.
Dated: February 23, 2012.
Tracey L. Thompson,
Acting Director, Office of Sustainable
Fisheries, National Marine Fisheries Service.
[FR Doc. 2012–4642 Filed 2–27–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
[FR Doc. 2012–4703 Filed 2–27–12; 8:45 am]
BILLING CODE 3510–22–P
RIN 0648–XB040
DEPARTMENT OF COMMERCE
Marine Mammals; File Nos. 1076–1789
and 14502
National Oceanic and Atmospheric
Administration
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; issuance of permit
amendments.
AGENCY:
RIN 0648–XB011
Mid-Atlantic Fishery Management
Council (MAFMC); Public Meeting;
Correction
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice of revision of a public
meeting.
AGENCY:
The Mid-Atlantic Fishery
Management Council’s (Council) AdHoc Atlantic Sturgeon Committee will
hold a meeting.
DATES: The meeting will be held on
March 19, 2012, from 10 a.m. until 4
p.m.
ADDRESSES: The meeting will be held at
Four Points by Sheraton BWI Airport,
7032 Elm Road, Baltimore, MD 21240;
telephone: (410) 859–3300.
Council address: Mid-Atlantic Fishery
Management Council, 800 N. State
Street Suite 201, Dover, DE 19901;
telephone: (302) 674–2331.
FOR FURTHER INFORMATION CONTACT:
Christopher M. Moore Ph.D., Executive
Director, Mid-Atlantic Fishery
Management Council, 800 N. State
Street Suite 201, Dover, DE 19901;
telephone: (302) 526–5255.
SUPPLEMENTARY INFORMATION: The
original notice published in the Federal
Register on February 17, 2012 (77 FR
9628). The date of the meeting changed
from March 6, 2012 to March 19, 2012.
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SUMMARY:
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Notice is hereby given that
the Alliance of Marine Mammal Parks
and Aquariums (The Alliance), 2850
Ranch Reserve Lane, Westminster,
Colorado 80234 (Kristi West, Ph.D.,
Principal Investigator) and Russell
Fielding, Ph.D., Department of
Geography, University of Denver, 2050
E. Iliff Avenue, Denver, CO 80208, have
been issued minor amendments to
Scientific Research Permit Nos. 1076–
1789 and 14502.
ADDRESSES: The amendment and related
documents are available for review
upon written request or by appointment
in the following offices:
Permits and Conservation Division,
Office of Protected Resources, NMFS,
1315 East-West Highway, Room 13705,
Silver Spring, MD 20910; phone (301)
427–8401; fax (301) 713–0376; and
Northwest Region, NMFS, 7600 Sand
Point Way NE., BIN C15700, Bldg. 1,
Seattle, WA 98115–0700; phone (206)
526–6150; fax (206) 526–6426.
FOR FURTHER INFORMATION CONTACT:
Jennifer Skidmore, Amy Sloan or Kristy
Beard, (301) 427–8401.
SUPPLEMENTARY INFORMATION: The
requested amendments have been
granted under the authority of the
Marine Mammal Protection Act of 1972,
as amended (16 U.S.C. 1361 et seq.) and
SUMMARY:
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the regulations governing the taking and
importing of marine mammals (50 CFR
part 216).
Permit No. 1076–1789: This permit,
issued on March 13, 2007 (72 FR
13092), authorized the receipt, import
and export of marine mammal
specimens (cetaceans and pinnipeds,
except for walrus) under the jurisdiction
of NMFS to study and document the
health and biology of wild marine
mammals as well as those marine
mammals maintained in public display,
research, or stranding facilities or from
samples taken during other permitted
research through February 29, 2012.
This minor amendment (No. 1076–
1789–01) extends the duration of the
permit through February 28, 2013, but
does not change any other terms or
conditions of the permit.
Permit No. 14502: This permit, issued
on June 17, 2011 (72 FR 13092),
authorized the importation of samples
from Risso’s (Grampus griseus), spinner
(Stenella longirostris), and spotted (S.
frontalis) dolphins and short-finned
pilot whales (Globicephala
macrorhynchus) for the purpose of
scientific research through June 17,
2012. This minor amendment (No.
14502–01) extends the duration of the
permit through June 17, 2013, but does
not change any other terms or
conditions of the permit.
Dated: February 22, 2012.
P. Michael Payne,
Chief, Permits and Conservation Division,
Office of Protected Resources, National
Marine Fisheries Service.
[FR Doc. 2012–4700 Filed 2–27–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XA950
Takes of Marine Mammals Incidental to
Specified Activities; Navy Research,
Development, Test and Evaluation
Activities at the Naval Surface Warfare
Center Panama City Division
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; proposed incidental
harassment authorization; request for
comments.
AGENCY:
NMFS has received an
application from the U.S. Navy (Navy)
for an Incidental Harassment
Authorization (IHA) to take marine
mammals, by harassment, incidental to
SUMMARY:
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Background
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 taking 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 and amended the definition
of ‘‘harassment’’ as it applies to a
‘‘military readiness activity’’ to read as
follows (Section 3(18)(B) of the MMPA):
(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].
Section 101(a)(5)(D) of the MMPA
established an expedited process by
which citizens of the United States can
apply for an authorization to
incidentally take small numbers of
marine mammals by harassment.
Section 101(a)(5)(D) establishes a 45-day
time limit for NMFS review of an
application followed by a 30-day public
notice and comment period on any
proposed authorizations for the
incidental harassment of marine
mammals. Within 45 days of the close
of the comment period, NMFS must
either issue or deny the authorization.
Sections 101(a)(5)(A) and (D) of the
MMPA (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce (Secretary)
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)
if certain findings are made and
regulations are issued or, if the taking is
limited to harassment, notice of a
Summary of Request
NMFS received an application on
December 28, 2011, from the Navy for
the taking, by harassment, of marine
mammals incidental to conducting
testing of the AN/AQS–20A Mine
Reconnaissance Sonar System (hereafter
referred to as the Q–20) in the Naval
Surface Warfare Center, Panama City
Division (NSWC PCD) testing range in
the Gulf of Mexico (GOM) from April
conducting research, development, test
and evaluation (RDT&E) activities at the
Naval Surface Warfare Center Panama
City Division (NSWC PCD). Pursuant to
the Marine Mammal Protection Act
(MMPA), NMFS is requesting comments
on its proposal to issue an IHA to the
Navy to incidentally harass, by Level B
Harassment only, marine mammals
during the specified activity.
DATES: Comments and information must
be received no later than March 29,
2012.
Comments on the
application should be addressed to
Michael Payne, Chief, Permits and
Conservation Division, Office of
Protected Resources, National Marine
Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910. The
mailbox address for providing email
comments is itp.guan@noaa.gov. NMFS
is not responsible for email comments
sent to addresses other than the one
provided here. Comments sent via
email, including all attachments, must
not exceed a 10-megabyte file size.
Instructions: All comments received
are a part of the public record and will
generally be posted to https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm without change. All
Personal Identifying Information (for
example, name, address, etc.)
voluntarily submitted by the commenter
may be publicly accessible. Do not
submit Confidential Business
Information or otherwise sensitive or
protected information.
A copy of the application containing
a list of the references used in this
document may be obtained by writing to
the address specified above, telephoning
the contact listed below (see FOR
FURTHER INFORMATION CONTACT), or
visiting https://www.nmfs.noaa.gov/pr/
permits/incidental.htm. Documents
cited in this notice may also be viewed,
by appointment, during regular business
hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT:
Shane Guan, Office of Protected
Resources, NMFS, (301) 427–8401.
SUPPLEMENTARY INFORMATION:
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ADDRESSES:
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2012 through April 2013. The Q–20
sonar test activities are proposed to be
conducted in the non-territorial waters
of the United States (beyond 12 nautical
miles) in the Gulf of Mexico (GOM, see
Figure 2–1 of the Navy IHA
application).
Description of the Specific Activity
The purpose of the Navy’s activities is
to meet the developmental testing
requirements of the Q–20 system by
verifying its performance in a realistic
ocean and threat environment and
supporting its integration with the
Remote Multi-Mission Vehicle (RMMV)
and ultimately the Littoral Combat Ship
(LCS). Testing would include
component, subsystem-level, and fullscale system testing in an operational
environment.
The need for the proposed activities is
to support the timely deployment of the
Q–20 to the operational Navy for Mine
Countermeasure (MCM) activities
abroad, allowing the Navy to meet its
statutory mission to deploy naval forces
equipped and trained to meet existing
and emergent threats worldwide and to
enhance its ability to operate jointly
with other components of the armed
forces.
The proposed activities are to test the
Q–20 from the RMMV and from
surrogate platforms such as a small
surface vessel or helicopter. The RMMV
or surrogate platforms will be deployed
from the Navy’s new LCS or its
surrogates. The Navy is evaluating
potential environmental effects
associated with the Q–20 test activities
proposed for the Q–20 Study Area (see
below for detailed description of the
Study Area), which includes nonterritorial waters of Military Warning
Area 151 (W–151; includes Panama City
Operating Area). Q–20 test activities
occur at sea in the waters present within
the Q–20 Study Area. No hazardous
waste is generated at sea during Q–20
test activities. There are two
components associated with the Q–20
test activities, which are addressed
below.
Surface Operations
A significant portion of Q–20 test
activities rely on surface operations to
successfully complete the missions. The
Proposed Action includes up to 420
hours of surface operations during
active sonar testing per year in the Q–
20 Study Area. Other surface operations
occur when sonar is not active. Three
subcategories make up surface
operations: support activities; tows; and
deployment and recovery of equipment.
Testing requiring surface operations
may include a single test event (one day
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of activity) or a series of test events
spread out over several days. The size
of the surface vessels varies in
accordance with the test requirements
and vessel availability. Often multiple
surface craft are required to support a
single test event.
Acting as a support platform for
testing, surface vessels would be
utilized to carry test equipment and
personnel to and from the test sites and
are also used to secure and monitor the
designated test area. Normally, these
vessels remain on site and return to port
following the completion of the test;
occasionally, however, they remain on
station throughout the duration of the
test cycle for guarding sensitive
equipment in the water.
Additional vessels would be used for
support activities that include tows, and
deployment and recovery of equipment.
Tows involve either transporting the
system to the designated test area where
it is deployed and towed over a prepositioned inert minefield or towing the
system from ashore for operation in the
designated test area. Surface vessels are
also used to perform the deployment
and recovery of the RMMV, mine-like
objects, and other test systems. Surface
vessels that are used in this manner
normally return to port the same day.
However, this is test dependent, and
under certain circumstance the surface
vessel may be required to remain on site
for an extended period of time.
Sonar Operations
For the proposed action, the Navy
would test the Q–20 for up to 420 hours
of active sonar use for 12 months
starting in April 2012. Q–20 sonar
operations involve the testing of various
sonar systems at sea as a means of
demonstrating the systems’ software
capability to detect, locate, and
characterize mine-like objects under
various environmental conditions. The
data collected is used to validate the
sonar systems’ effectiveness and
capability to meet its mission.
As sound travels through water, it
creates a series of pressure disturbances.
Frequency is the number of complete
cycles a sound or pressure wave occurs
per unit of time (measured in cycles per
second, or hertz (Hz)). The Navy has
characterized low, mid, or high
frequency active sonars as follows:
• Low-frequency active sonar
(LFAS)—Below 1 kilohertz (kHz) (lowfrequency sound sources will not be
used during any Q–20 test operations)
• Mid-frequency active sonar
(LFAS)—From 1 to 10 kHz (midfrequency source sources will not be
used during any Q–20 test operations)
• High-frequency active sonar
(HFAS)—Above 10 kHz (only highfrequency sound sources would be used
during Q–20 test operations)
The Q–20 sonar systems proposed to
be tested within the Q–20 Study Area
range in frequencies from 35 kHz to >
200 kHz, therefore, these are HFAS
systems. Those systems that operate at
very high frequencies (i.e., > 200 kHz),
well above the hearing sensitivities of
any marine mammals, are not
considered to affect marine mammals.
Therefore, they are not included in this
document. The source levels associated
with Q–20 sonar systems that could
affect marine mammals range from 207
decibels (dB) re 1 micro pascal (mPa) at
1 meter (m) to 212 dB re 1 mPa at 1 m.
Operating parameters of the Q–20 sonar
systems can be found in Appendix A,
Supplemental Information for
Underwater Noise Analysis of the
Navy’s IHA application.
The Q–20 Study Area includes Target
and Operational Test Fields located in
W–151, an area within the Gulf of
Mexico (GOM) subject to military
operations which also encompasses the
Panama City Operating Area (Figure 2–
1 of the Navy’s IHA application). The
Q–20 test activities will be conducted in
the non-territorial waters off the United
States (beyond 12 nautical miles) in the
GOM. The locations and environments
include:
• Wide coastal shelf to 183 meters (m)
[600 feet (ft)].
• Water temperature range of 27
degrees Celsius (°C) [80 degrees
Fahrenheit (°F)] in summer to 10 °C (50
°F) in winter.
• Mostly sandy bottom and good
underwater visibility.
• Seas less than 0.91 m (3 ft) 80
percent of the time in summer and 50
percent of the time in winter.
The Navy requests an IHA for a time
period of one year beginning April,
2012. A total of 42 Q–20 test days will
be conducted with a maximum sonar
operation of 10 hours in a single day.
Description of Marine Mammals in the
Area of the Specified Activity
There are 29 marine mammal species
under NMFS’ jurisdiction that may
occur in the Q–20 Study Area (Table 1).
These include 7 mysticetes (baleen
whales) and 22 odontocetes (toothed
whales). Table 1 also includes the
Federal status of these marine mammal
species. Six of these marine mammal
species under NMFS’ jurisdiction are
also listed as federally endangered
under the Endangered Species Act
(ESA) and could potentially occur in the
Study Area: the humpback whale, North
Atlantic right whale, sei whale, fin
whale, blue whale, and sperm whale. Of
these 29 species with occurrence
records in the Q–20 Study Area, 22
species regularly occur there. These 22
species are: Bryde’s whale, sperm
whale, pygmy sperm whale, dwarf
sperm whale, Cuvier’s beaked whale,
Gervais’ beaked whale, Sowerby’s
beaked whale, Blainville’s beaked
whale, killer whale, false killer whale,
pygmy killer whale, short-finned pilot
whale, Risso’s dolphin, melon-headed
whale, rough-toothed dolphin,
bottlenose dolphin, Atlantic spotted
dolphin, pantropical spotted dolphin,
striped dolphin, spinner dolphin,
Clymene dolphin, and Fraser’s dolphin.
The remaining 7 species (i.e., North
Atlantic right whale, humpback whale,
sei whale, fin whale, blue whale, minke
whale, and True’s beaked whale) are
extralimital and are excluded from
further consideration of impacts from
the NSWC PCD Q–20 testing analysis.
TABLE 1—MARINE MAMMAL SPECIES POTENTIALLY FOUND IN THE Q–20 STUDY AREA
Family and scientific name
Common name
Federal status
Order Cetacea
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Suborder Mysticeti (baleen whales)
Eubalaena glacialis .................................................................
Megaptera novaeangliae ........................................................
Balaenoptera acutorostrata .....................................................
B. brydei ..................................................................................
B. borealis ...............................................................................
B. physalus .............................................................................
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North Atlantic right whale ......................................................
Humpback whale ...................................................................
Minke whale..
Bryde’s whale..
Sei whale ...............................................................................
Fin whale ...............................................................................
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Endangered
Endangered.
Endangered.
Endangered.
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TABLE 1—MARINE MAMMAL SPECIES POTENTIALLY FOUND IN THE Q–20 STUDY AREA—Continued
Family and scientific name
Common name
Federal status
B. musculus ............................................................................
Blue whale .............................................................................
Endangered.
Suborder Odontoceti (toothed whales)
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Physeter macrocephalus ........................................................
Kogia breviceps ......................................................................
K. sima ....................................................................................
Ziphius cavirostris ...................................................................
Mesoplodon europaeus ..........................................................
M. Mirus ..................................................................................
M. bidens ................................................................................
M. densirostris .........................................................................
Steno bredanensis ..................................................................
Tursiops truncatus ..................................................................
Stenella attenuata ...................................................................
S. frontalis ...............................................................................
S. longirostris ..........................................................................
S. clymene ..............................................................................
S. coeruleoalba .......................................................................
Lagenodephis hosei ................................................................
Grampus griseus .....................................................................
Peponocephala electra ...........................................................
Feresa attenuata .....................................................................
Pseudorca crassidens .............................................................
Orcinus orca ............................................................................
Globicephala macrorhynchus .................................................
The information contained herein
relies heavily on the data gathered in
the Marine Resource Assessments
(MRAs). The Navy Marine Resources
Assessment (MRA) program was
implemented by the Commander,
United States Fleet Forces Command, to
collect data and information on the
protected and commercial marine
resources found in the Department of
the Navy’s (DON’s) operating areas.
Specifically, the goal of the MRA
program is to describe and document
the marine resources present in each of
the Navy’s Operating Areas. As such, an
MRA has been completed for the GOM
Testing and Training Areas, which
comprise three adjacent Operating
Areas, one of which is the Panama City
Operating Area (DON, 2007). The DON
2007 is the most current MRA for the
GOM.
The MRA represents a compilation
and synthesis of available scientific
literature (e.g., journals, periodicals,
theses, dissertations, project reports,
and other technical reports published by
government agencies, private
businesses, or consulting firms) and
NMFS reports, including stock
assessment reports (SARs), recovery
plans, and survey reports. The MRAs
summarize the physical environment
(e.g., marine geology, circulation and
currents, hydrography, and plankton
and primary productivity) for each test
area. In addition, an in-depth discussion
of the biological environment (marine
mammals, sea turtles, fish, and EFH), as
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Sperm whale ..........................................................................
Pygmy sperm whale.
Dwarf sperm whale.
Cuvier’s beaked whale.
Gervais’ beaked whale.
True’s beaked whale.
Sowerby’s beaked whale.
Blainville’s beaked whale.
Rough-toothed dolphin.
Bottlenose dolphin.
Pantropical spotted dolphin.
Atlantic spotted dolphin.
Spinner dolphin.
Clymene dolphin.
Striped dolphin.
Fraser’s dolphin.
Risso’s dolphin.
Melon-headed whale.
Pygmy killer whale.
False killer whale.
Killer whale.
Short-finned pilot whale.
well as fishing grounds (recreational
and commercial) and other areas of
interest (e.g., maritime boundaries,
navigable waters, marine managed
areas, recreational diving sites) are also
provided. Where applicable, the
information contained in the MRA was
used for analyses in this document.
A detailed description of marine
mammal density estimates and their
distribution in the Q–20 Study Area is
provided in the Navy’s Q–20 IHA
application.
A 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
document. A summary is included
below.
Sound is a wave of pressure variations
propagating through a medium (for the
sonar considered in this proposed rule,
the medium is marine 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, it
is derived from ratios of pressures; the
standard reference pressure for
underwater sound is 1 mPa; for airborne
sound, the standard reference pressure
is 20 mPa (Urick, 1983).
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Endangered.
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 power (e.g., 20 dB is
a 100-fold increase, 30 dB is a 1,000-fold
increase). Humans perceive a 10-dB
increase in noise as a doubling of sound
level, or a 10 dB decrease in noise as a
halving of sound level. The term ‘‘sound
pressure level’’ implies a decibel
measure and a reference pressure that is
used as the denominator of the ratio.
Throughout this document, NMFS uses
1 mPa as a standard reference pressure
unless noted otherwise.
It is important to note that decibels
underwater and decibels in air are not
the same and cannot be directly
compared. To estimate a comparison
between sound in air and underwater,
because of the different densities of air
and water and the different decibel
standards (i.e., reference pressures) in
water and air, a sound with the same
intensity (i.e., power) in air and in water
would be approximately 63 dB lower in
air. Thus, a sound that is 160 dB loud
underwater would have the same
approximate effective intensity as a
sound that is 97 dB loud in air.
Sound frequency is measured in
cycles per second, or Hertz (abbreviated
Hz), and is analogous to musical pitch;
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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 and ultrasonic 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;’’ airguns are an example of
a broadband sound source and 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. Based on available
behavioral data, audiograms derived
using auditory evoked potential,
anatomical modeling, and other data,
Southall et al. (2007) designate
‘‘functional hearing groups’’ and
estimate the lower and upper
frequencies of functional hearing of the
groups. Further, the frequency range in
which each group’s hearing is estimated
as being most sensitive is represented in
the flat part of the M-weighting
functions developed for each group. The
functional groups and the associated
frequencies are indicated below:
• Low-frequency cetaceans (13
species of mysticetes): Functional
hearing is estimated to occur between
approximately 7 Hz and 22 kHz.
• Mid-frequency cetaceans (32
species of dolphins, six species of larger
toothed whales, and 19 species of
beaked and bottlenose whales):
Functional hearing is estimated to occur
between approximately 150 Hz and 160
kHz.
• High-frequency cetaceans (eight
species of true porpoises, six species of
river dolphins, Kogia, the franciscana,
and four species of cephalorhynchids):
Functional hearing is estimated to occur
between approximately 200 Hz and 180
kHz.
• Pinnipeds in Water: Functional
hearing is estimated to occur between
approximately 75 Hz and 75 kHz, with
the greatest sensitivity between
approximately 700 Hz and 20 kHz.
• Pinnipeds in Air: Functional
hearing is estimated to occur between
approximately 75 Hz and 30 kHz.
Because ears adapted to function
underwater are physiologically different
from human ears, comparisons using
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decibel measurements in air would still
not be adequate to describe the effects
of a sound on a whale. When sound
travels away from its source, its
loudness decreases as the distance
traveled (propagates) by the sound
increases. Thus, the loudness of a sound
at its source is higher than the loudness
of that same sound a kilometer distant.
Acousticians often refer to the loudness
of a sound at its source (typically
measured one meter from the source) as
the source level and the loudness of
sound elsewhere as the received level.
For example, a humpback whale three
kilometers from an airgun that has a
source level of 230 dB may only be
exposed to sound that is 160 dB loud,
depending on how the sound
propagates. As a result, it is important
not to confuse source levels and
received levels when discussing the
loudness of sound in the ocean.
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 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 Document
This section includes a brief
explanation of the two sound
measurements (sound pressure level
(SPL) and sound exposure level (SEL))
frequently used in the discussions of
acoustic effects in this document.
SPL
Sound pressure is the sound force per
unit area, and is usually measured in
microPa, 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 ratio of
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a measured sound pressure and a
reference level. The commonly used
reference pressure level in underwater
acoustics is 1 mPa, and the units for
SPLs are dB re: 1 mPa.
SPL (in dB) = 20 log (pressure/reference
pressure)
SPL is an instantaneous measurement
and can be expressed as the peak, the
peak-peak, or the root mean square
(rms). Root mean square, 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
document refer to the root mean square.
SPL does not take the duration of a
sound 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).
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 microPa2-s.
SEL = SPL + 10 log(duration in seconds)
As applied to tactical 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 total SEL. The total 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
in SEL.
Potential Impacts to Marine Mammal
Species
The Navy considers that the proposed
Q–20 sonar testing activities in the Q–
20 Study Area could potentially result
in harassment to marine mammals.
Although surface operations related to
sonar testing involve ship movement in
the vicinity of the Q–20 test area, NMFS
considers it unlikely that ship strike
could occur as analyzed below.
Surface Operations
Typical operations occurring at the
surface include the deployment or
towing of mine countermeasures (MCM)
equipment, retrieval of equipment, and
clearing and monitoring for nonparticipating vessels. As such, the
potential exists for a ship to strike a
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marine mammal while conducting
surface operations. In an effort to reduce
the likelihood of a vessel strike, the
mitigation and monitoring measures
discussed below would be
implemented.
Collisions with commercial and U.S.
Navy vessels can cause major wounds
and may occasionally cause fatalities to
marine mammals. 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). Laist et al. (2001)
identified 11 species known to be hit by
ships worldwide. Of these species, fin
whales are struck most frequently;
followed by right whales, humpback
whales, sperm whales, and gray whales.
More specifically, from 1975 through
1996, there were 31 dead whale
strandings involving four large whales
along the GOM coastline. Stranded
animals included two sei whales, four
minke whales, eight Bryde’s whales,
and 17 sperm whales. Only one of the
stranded animals, a sperm whale with
propeller wounds found in Louisiana on
9 March 1990, was identified as
stranding as a result of a possible ship
strike (Laist et al., 2001). In addition,
from 1999 through 2003, there was only
one stranding involving a false killer
whale in the northern GOM (Alabama
1999) (Waring et al., 2006). According to
the 2010 Stock Assessment Report
(NMFS 2011), during 2009 there was
one known Bryde’s whale mortality as
a result of a ship strike. Otherwise, no
other marine mammal that is likely to
occur in the northern GOM has been
reported as either seriously or fatally
injured as a result of a ship strike from
1999 through 2009 (Waring et al., 2007).
It is unlikely that activities in nonterritorial waters will result in a ship
strike because of the nature of the
operations and size of the vessels. For
example, the hours of surface operations
take into consideration operation times
for multiple vessels during each test
event. These vessels range in size from
small Rigid Hull Inflatable Boat (RHIB)
to surface vessels of approximately 420
feet. The majority of these vessels are
small RHIBs and medium-sized vessels.
A large proportion of the timeframe for
the Q–20 test events include periods
when ships remain stationary within the
test site.
The greatest time spent in transit for
tests includes navigation to and from
the sites. At these times, the Navy
follows standard operating procedures
(SOPs). The captain and other crew
members keep watch during ship
transits to avoid objects in the water.
Furthermore, with the implementation
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of the proposed mitigation and
monitoring measures described below,
NMFS believes that it is unlikely vessel
strikes would occur. Consequently,
because of the nature of the surface
operations and the size of the vessels,
the proposed mitigation and monitoring
measures, and the fact that cetaceans
typically more vulnerable to ship strikes
are not likely to be in the project area,
the NMFS concludes that ship strikes
are unlikely to occur in the Q–20 Study
Area.
Acoustic Effects: Exposure to Sonar
For activities involving active tactical
sonar, NMFS’s analysis will identify the
probability of lethal responses, physical
trauma, sensory impairment (permanent
and temporary threshold shifts and
acoustic masking), physiological
responses (particular stress responses),
behavioral disturbance (that rises to the
level of harassment), and social
responses that would be classified as
behavioral harassment or injury and/or
would be likely to adversely affect the
species or stock through effects on
annual rates of recruitment or survival.
In this section, we will focus
qualitatively on the different ways that
exposure to sonar signals may affect
marine mammals. Then, in the
Estimated Take of Marine Mammals
section, NMFS will relate the potential
effects on marine mammals from sonar
exposure to the MMPA regulatory
definitions of Level A and Level B
Harassment and attempt to quantify
those effects.
Direct Physiological Effects
Based on the literature, there are two
basic ways that Navy sonar 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 recognize them)
following exposure to a sufficiently
intense sound, 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
recovery), occurs in specific frequency
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ranges (e.g., 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 by only 6
dB or reduced by 30 dB). PTS is
permanent (i.e., there is no recovery),
but also occurs in a specific frequency
range and amount as mentioned in the
TTS description.
The following physiological
mechanisms are thought to play a role
in inducing auditory TSs: Effects on
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 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. For continuous
sounds, exposures of equal energy (the
same SEL) will lead to approximately
equal effects. For intermittent sounds,
less TS will occur than from a
continuous exposure with the same
energy (some recovery will occur
between exposures) (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, very prolonged exposure
to sound 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
Navy sonar, 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,
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
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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
cetaceans, published data are limited to
the captive bottlenose dolphin and
beluga whale (Finneran et al., 2000,
2002b, 2005a; Schlundt et al., 2000;
Nachtigall et al., 2003, 2004).
Marine mammal hearing plays a
critical role in communication with
conspecifics, and interpreting
environmental cues for purposes such
as predator avoidance and prey capture.
Depending on the frequency range of
TTS degree (dB), duration, 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 takes place during
a time when the animal is traveling
through the open ocean, 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
a 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 long term condition. Of
note, reduced hearing sensitivity as a
simple function of development and
aging has been observed in marine
mammals, as well as humans and other
taxa (Southall et al., 2007), so we can
infer that strategies exist for coping with
this condition to some degree, though
likely not without cost. There is no
empirical evidence that exposure to
Navy sonar can cause PTS in any
marine mammals; instead the
probability of PTS has been inferred
from studies of TTS (see Richardson et
al., 1995).
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
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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., 2001). 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.
Recent work conducted by Crum et al.
(2005) demonstrated the possibility of
rectified diffusion for short duration
signals, but at sound exposure levels
and tissue saturation levels that are
improbable to occur in a diving marine
mammal. 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. 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). In this
scenario, the rate of ascent would need
to be sufficiently rapid to compromise
behavioral or physiological protections
against nitrogen bubble formation.
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
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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, 2002).
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 (Hooker
et al., 2011). However, Jepson et al.
(2003, 2005) and Fernandez et al. (2004,
2005) 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. A recent review of evidence
for gas-bubble incidence in marine
mammal tissues suggest that diving
mammals vary their physiological
responses according to multiple
stressors, and that the perspective on
marine mammal diving physiology
should change from simply minimizing
nitrogen loading to management of the
nitrogen load (Hooker et al., 2011). This
suggests several avenues for further
study, ranging from the effects of gas
bubbles at molecular, cellular and organ
function levels, to comparative studies
relating the presence/absence of gas
bubbles to diving behavior. More
information regarding hypotheses that
attempt to explain how behavioral
responses to Navy sonar can lead to
strandings is included in the
Behaviorally Mediated Bubble Growth
section, after the summary of strandings.
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; Clark et
al., 2009). 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
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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 also decreases. This principle
is also expected to apply to marine
mammals because of common
biomechanical cochlear properties
across taxa.
Richardson et al. (1995) 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 odontocetes
(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-tomoderate frequencies they use to
communicate (Zaitseva et al., 1980).
As mentioned previously, the
functional hearing ranges of mysticetes
(baleen whales) and odontocetes
(toothed whales) all encompass the
frequencies of the sonar sources used in
the Navy’s Q–20 test activities.
Additionally, almost all species’ vocal
repertoires span across the frequencies
of the 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.
However, because the pulse length and
duty cycle of the Navy sonar signals are
of short duration and would not be
continuous, masking is unlikely to
occur as a result of exposure to these
signals during the Q–20 test activities in
the designated Q–20 Study Area.
Impaired Communication
In addition to making it more difficult
for animals to perceive acoustic cues in
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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 are more important
than detecting a vocalization
(Brenowitz, 1982; Brumm et al., 2004;
Dooling, 2004; Marten and Marler, 1977;
Patricelli et al., 2006). Most animals that
vocalize have evolved an ability to make
vocal adjustments to their vocalizations
to increase the signal-to-noise ratio,
active space, and recognizability of their
vocalizations in the face of temporary
changes in background noise (Brumm et
al., 2004; Patricelli et al., 2006).
Vocalizing animals will make one or
more of the following adjustments to
their vocalizations: Adjust the frequency
structure; adjust the amplitude; adjust
temporal structure; or adjust 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;
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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
response.
In the case of many stressors, an
animal’s first and 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 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 associate with
‘‘stress.’’ These responses have a
relatively short duration and may or
may not have significant long-term
effects on an animal’s welfare.
An animal’s third line of defense to
stressors involves its neuroendocrine or
sympathetic nervous systems; the
system that has received the most study
has been the hypothalmus-pituitaryadrenal 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) and 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; 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
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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 functions, which impair
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’’ (sensu Seyle, 1950) or
‘‘allostatic loading’’ (sensu McEwen and
Wingfield, 2003). This pathological state
will last until the animal replenishes its
biotic reserves sufficient to restore
normal function.
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 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). Although no information has
been collected on the physiological
responses of marine mammals to
exposure to anthropogenic sounds,
studies of other marine animals and
terrestrial animals would 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 midfrequency 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 physiology
stress responses of endangered Sonoran
pronghorn to military overflights. Smith
et al. (2004a, 2004b) identified noise
induced physiological transient stress
responses in hearing-specialist fish that
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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
cetaceans 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 cetaceans 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
be as significant as behavioral responses
to TTS.
Behavioral Disturbance
Behavioral responses to sound are
highly variable and context-specific.
Exposure of marine mammals to sound
sources can result in (but is not limited
to) the following observable responses:
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).
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 type affects
whether it is less likely (habituation) or
more likely (sensitization) to respond to
certain sounds in the future (animals
can also be innately predisposed 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
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(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.
There are only a few empirical studies
of behavioral responses of free-living
cetaceans to military sonar being
conducted to date, due to the difficulties
in implementing experimental protocols
on wild marine mammals.
An opportunistic observation was
made on a tagged Blainville’s beaked
whale (Mesoplodon densirostris) before,
during, and after a multi-day naval
exercises involving tactical midfrequency sonars within the U.S. Navy’s
sonar testing range at the Atlantic
Undersea Test and Evaluation Center
(AUTEC), in the Tongue of the Ocean
near Andros Island in the Bahamas
(Tyack et al., 2011). The adult male
whale was tagged with a satellite
transmitter tag on May 7, 2009. During
the 72 hrs before the sonar exercise
started, the mean distance from whale to
the center of the AUTEC range was
approximately 37 km. During the 72 hrs
sonar exercise, the whale moved several
tens of km farther away (mean distance
approximately 54 km). The received
sound levels at the tagged whale during
sonar exposure were estimated to be 146
dB re 1 mPa at the highest level. The
tagged whale slowly returned for several
days after the exercise stopped (mean
distance approximately 29 km) from 0–
72 hours after the exercise stopped
(Tyack et al., 2011).
In the past several years, controlled
exposure experiments (CEE) on marine
mammal behavioral responses to
military sonar signals using acoustic
tags have been started in the Bahamas,
the Mediterranean Sea, southern
California, and Norway. These
behavioral response studies (BRS),
though still in their early stages, have
provided some preliminary insights into
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cetacean behavioral disturbances when
exposed to simulated and actual
military sonar signals.
In 2007 and 2008, two Blainville’s
beaked whales were tagged in the
AUTEC range and exposed to simulated
mid-frequency sonar signals, killer
whale (Orcinus orca) recordings (in
2007), and pseudo-random noise (PRN,
in 2008) (Tyack et al., 2011). For the
simulated mid-frequency exposure BRS,
the tagged whale stopped clicking
during its foraging dive after 9 minutes
when the received level reached 138 dB
SPL, or a cumulative SEL value of 142
dB re 1 mPa2-s. Once the whale stopped
clicking, it ascended slowly, moving
away from the sound source. The whale
surfaced and remained in the area for
approximately 2 hours before making
another foraging dive (Tyack et al.,
2011).
The same beaked whale was exposed
to killer whale sound recording during
its subsequent deep foraging dive. The
whale stopped clicking about 1 minute
after the received level of the killer
whale sound reached 98 dB SPL, just
above the ambient noise level at the
whale. The whale then made a long and
slow ascent. After surfacing, the whale
continued to swim away from the
playback location for 10 hours (Tyack et
al., 2011).
In 2008, a Blainville’s beaked was
tagged and exposed with PRN that has
the same frequency band as the
simulated mid-frequency sonar signal.
The received level at the whale ranged
from inaudible to 142 dB SPL (144 dB
cumulative SEL). The whale stopped
clicking less than 2 minutes after
exposure to the last transmission and
ascended slowly to approximately
600 m. The whale appeared to stop at
this depth, at which time the tag
unexpectedly released from the whale
(Tyack et al., 2011).
During CEEs of the BRS off Norway,
social behavioral responses of pilot
whales and killer whales to tagging and
sonar exposure were investigated. Sonar
exposure was sampled for 3 pilot whale
(Globicephala spp.) groups and 1 group
of killer whales. Results show that when
exposed to sonar signals, pilot whales
showed a preference for larger groups
with medium-low surfacing synchrony,
while starting logging, spyhopping and
milling. While killer whales showed the
opposite pattern, maintaining
asynchronous patterns of surface
behavior: decreased surfacing
synchrony, increased spacing, decreased
group size, tailslaps and loggings (Visser
et al., 2011).
Although the small sample size of
these CEEs reported here is too small to
make firm conclusions about differential
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12019
The reports 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
HFAS/MFAS) including: Vessel noise,
drilling and machinery playback, low
frequency M-sequences (sine wave with
multiple phase reversals) playback, low
frequency active sonar playback, drill
vessels, Acoustic Thermometry of
Ocean Climate (ATOC) source, and nonpulse playbacks. These reports 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, however,
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 reports that address responses of
Behavioral Responses
mid-frequency cetaceans to non-pulse
sounds include data gathered both in
Southall et al., (2007) reports the
results of the efforts of a panel of experts the field and the laboratory and related
to several different sound sources (of
in acoustic research from behavioral,
varying similarity to HFAS/MFAS)
physiological, and physical disciplines
including: Pingers, drilling playbacks,
that convened and reviewed the
vessel and ice-breaking noise, vessel
available literature on marine mammal
noise, Acoustic Harassment Devices
hearing and physiological and
(AHDs), Acoustic Deterrent Devices
behavioral responses to man-made
(ADDs), HFAS/MFAS, and non-pulse
sound with the goal of proposing
exposure criteria for certain effects. This bands and tones. Southall et al. were
unable to come to a clear conclusion
compilation of literature is very
regarding these reports. In some cases,
valuable, though Southall et al. note
animals in the field showed significant
that not all data is equal, some have
responses to received levels between 90
poor statistical power, insufficient
and 120 dB, while in other cases these
controls, and/or limited information on
responses were not seen in the 120 to
received levels, background noise, and
150 dB range. The disparity in results
other potentially important contextual
variables—such data were reviewed and was likely due to contextual variation
and the differences between the results
sometimes used for qualitative
in the field and laboratory data (animals
illustration, but were not included in
responded at lower levels in the field).
the quantitative analysis for the criteria
recommendations.
The reports that address the responses
In the Southall et al., (2007) report, for of high-frequency cetaceans to nonpulse sounds include data gathered both
the purposes of analyzing responses of
in the field and the laboratory and
marine mammals to anthropogenic
related to several different sound
sound and developing criteria, the
sources (of varying similarity to HFAS/
authors differentiate between single
MFAS) including: Acoustic harassment
pulse sounds, multiple pulse sounds,
devices, Acoustical Telemetry of Ocean
and non-pulse sounds. HFAS/MFAS
Climate (ATOC), wind turbine, vessel
sonar is considered a non-pulse sound.
noise, and construction noise. However,
Southall et al., (2007) summarize the
no conclusive results are available from
reports associated with low-, mid-, and
these reports. In some cases, high
high-frequency cetacean responses to
frequency cetaceans (harbor porpoises)
non-pulse sounds (there are no
pinnipeds in the Gulf of Mexico (GOM)) are observed to be quite sensitive to a
wide range of human sounds at very low
in Appendix C of their report
exposure RLs (90 to 120 dB). All
(incorporated by reference and
recorded exposures exceeding 140 dB
summarized in the three paragraphs
produced profound and sustained
below).
responses of cetaceans to military sonar
exposure, none of the results showed
that whales responded to sonar signals
with panicked flight. Instead, the
beaked whales exposed to simulated
sonar signals and killer whale sound
recording moved in a well oriented
direction away from the source towards
the deep water exit from the Tongue of
the Ocean (Tyack et al., 2011). In
addition, different species of cetaceans
exhibited different social behavioral
responses towards (close) vessel
presence and sonar signals, which elicit
different, potentially tailored and
species-specific responses (Visser et al.,
2011).
Much more qualitative information is
available on the avoidance responses of
free-living cetaceans to other acoustic
sources, like seismic airguns and lowfrequency active sonar, than midfrequency active sonar. Richardson et
al., (1995) noted that avoidance
reactions are the most obvious
manifestations of disturbance in marine
mammals.
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avoidance behavior in wild harbor
porpoises (Southall et al., 2007).
In addition to summarizing the
available data, the authors of Southall et
al. (2007) developed a severity scaling
system with the intent of ultimately
being able to assign some level of
biological significance to a response.
Following is a summary of their scoring
system, a comprehensive list of the
behaviors associated with each score
may be found in the report:
• 0–3 (Minor and/or brief behaviors)
includes, but is not limited to: No
response; minor changes in speed or
locomotion (but with no avoidance);
individual alert behavior; minor
cessation in vocal behavior; minor
changes in response to trained behaviors
(in laboratory).
• 4–6 (Behaviors with higher
potential to affect foraging,
reproduction, or survival) includes, but
is not limited to: Moderate changes in
speed, direction, or dive profile; brief
shift in group distribution; prolonged
cessation or modification of vocal
behavior (duration > duration of sound);
minor or moderate individual and/or
group avoidance of sound; brief
cessation of reproductive behavior; or
refusal to initiate trained tasks (in
laboratory).
• 7–9 (Behaviors considered likely to
affect the aforementioned vital rates)
includes, but are not limited to:
Extensive of prolonged aggressive
behavior; moderate, prolonged or
significant separation of females and
dependent offspring with disruption of
acoustic reunion mechanisms; long-term
avoidance of an area; outright panic,
stampede, stranding; threatening or
attacking sound source (in laboratory).
In Table 2 we have summarized the
scores that Southall et al. (2007)
assigned to the papers that reported
behavioral responses of low-frequency
cetaceans, mid-frequency cetaceans, and
high-frequency cetaceans to non-pulse
sounds.
TABLE 4—DATA COMPILED FROM THREE TABLES FROM SOUTHALL ET AL. (2007) INDICATING WHEN MARINE MAMMALS
(LOW-FREQUENCY CETACEAN = L, MID-FREQUENCY CETACEAN = M, AND HIGH-FREQUENCY CETACEAN = H) WERE
REPORTED AS HAVING A BEHAVIORAL RESPONSE OF THE INDICATED SEVERITY TO A NON-PULSE SOUND OF THE INDICATED RECEIVED LEVEL. AS DISCUSSED IN THE TEXT, RESPONSES ARE HIGHLY VARIABLE AND CONTEXT SPECIFIC
Received RMS sound pressure level (dB re 1 microPa)
80 to <90
90 to
<100
100 to
<110
110 to
<120
120 to
<130
130 to
<140
140 to
<150
150 to
<160
160 to
<170
170 to
<180
180 to
<190
190 to
<200
9
8
7
6
5
4
3
2
1
0
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Response
score
.................
.................
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H
.................
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L/H
.................
M
.................
L/H
.................
.................
M
.................
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L/H
.................
M
.................
L/H
.................
H
L/M
L
M
L/M/H
.................
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.................
L/M/H
.................
L/M/H
L/M
L/M
M
L/M/H
.................
M
.................
L/M/H
M
L/M
M
L
M
L/M/H
.................
.................
L
L
.................
.................
.................
L
.................
L
.................
M
L
L/H
.................
L
.................
L
.................
M
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.................
H
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M/H
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.................
M
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.................
M
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.................
M
.................
M
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M
...........
...........
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...........
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 little 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 unconsciously (for
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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).
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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 (Anser
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brachyrhynchus) in undisturbed habitat
gained body mass and had about a 46percent reproductive success 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. Similar
reductions in reproductive success have
been reported for mule deer (Odocoileus
hemionus) 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
jetfights (Luick et al., 1996), and caribou
disturbed by low-elevation jet flights
(Harrington and Veitch, 1992).
Similarly, a study of elk (Cervus
elaphus) 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 (Ursus
horribilis) reported that bears disturbed
by hikers reduced their energy intake by
an average of 12 kcal/min (50.2 × 103kJ/
min), and spent energy fleeing or acting
aggressively toward hikers (White et al.,
1999).
On a related note, many animals
perform vital functions, such as feeding,
resting, traveling, and socializing, on a
diel cycle (24-hr 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
one day and not recurring on
subsequent days is not considered
particularly severe unless it could
directly affect reproduction or survival
(Southall et al., 2007).
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). Marine mammals are
known to strand for a variety of reasons,
such as infectious agents, biotoxicosis,
starvation, fishery interaction, ship
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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
stranding are unknown (Geraci et al.,
1976; Eaton, 1979, Odell et al., 1980;
Best, 1982).
Several sources have published lists
of mass stranding events of cetaceans
during attempts 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
(IWC, 2005) identified 10 mass
stranding events of Cuvier’s beaked
whales that had been reported and one
mass stranding of four Baird’s beaked
whales (Berardius bairdii). The IWC
concluded that, out of eight stranding
events reported from the mid-1980s to
the summer of 2003, seven had been
associated with the use of midfrequency sonar, one of those seven had
been associated with the use of low
frequency sonar, and the remaining
stranding event had been associated
with the use of seismic airguns. None of
the strandings has been associated with
high frequency sonar such as the Q–20
sonar proposed to be tested in this
action. Therefore, NMFS does not
consider it likely that the proposed Q–
20 testing activity would cause marine
mammals to strand.
Effects on Marine Mammal Habitat
There are no areas within the NSWC
PCD that are specifically considered as
important physical habitat for marine
mammals.
The prey of marine mammals are
considered part of their habitat. The
Navy’s Final Environmental Impact
Statement and Overseas Environmental
Impact Statement (FEIS) on the
research, development, test and
evaluation activities in the NSWC PCD
study area contains a detailed
discussion of the potential effects to fish
from HFAS/MFAS. These effects are the
same as expected from the proposed Q–
20 sonar testing activities within the
same area.
The extent of data, and particularly
scientifically peer-reviewed data, on the
effects of high intensity sounds on fish
is limited. In considering the available
literature, the vast majority of fish
species studied to date are hearing
generalists and cannot hear sounds
above 500 to 1,500 Hz (depending upon
the species), and, therefore, behavioral
effects on these species from higher
frequency sounds are not likely.
Moreover, even those fish species that
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may hear above 1.5 kHz, such as a few
sciaenids and the clupeids (and
relatives), have relatively poor hearing
above 1.5 kHz as compared to their
hearing sensitivity at lower frequencies.
Therefore, even among the species that
have hearing ranges that overlap with
some mid- and high-frequency sounds,
it is likely that the fish will only
actually hear the sounds if the fish and
source are very close to one another.
Finally, since the vast majority of
sounds that are of biological relevance
to fish are below 1 kHz (e.g., Zelick et
al., 1999; Ladich and Popper, 2004),
even if a fish detects a mid-or highfrequency sound, these sounds will not
mask detection of lower frequency
biologically relevant sounds. Based on
the above information, there will likely
be few, if any, behavioral impacts on
fish.
Alternatively, it is possible that very
intense mid- and high-frequency signals
could have a physical impact on fish,
resulting in damage to the swim bladder
and other organ systems. However, even
these kinds of effects have only been
shown in a few cases in response to
explosives, and only when the fish has
been very close to the source. Such
effects have never been indicated in
response to any Navy sonar. Moreover,
at greater distances (the distance clearly
would depend on the intensity of the
signal from the source) there appears to
be little or no impact on fish, and
particularly no impact on fish that do
not have a swim bladder or other air
bubble that would be affected by rapid
pressure changes.
Proposed Mitigation Measures
In order to issue an incidental take
authorization (ITA) under Section
101(a)(5)(D) 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.’’ The National Defense
Authorization Act (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 Q–20
sonar testing activities described in the
Navy’s IHA application are considered
military readiness activities.
For the proposed Q–20 sonar testing
activities in the GOM, NMFS worked
with the Navy to develop mitigation
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measures. The Navy then proposed the
following mitigation measures, which
include a careful balancing of
minimizing impacts to marine mammals
with the likely effect of that measure on
personnel safety, practicality of
implementation, and impact on the
‘‘military-readiness activity’’.
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Personnel Training
Marine mammal mitigation training
for those who participate in the active
sonar activities is a key element of the
protective measures. The goal of this
training is for key personnel onboard
Navy platforms in the Q–20 Study Area
to understand the protective measures
and be competent to carry them out. The
Marine Species Awareness Training
(MSAT) is provided to all applicable
participants, where appropriate. The
program addresses environmental
protection, laws governing the
protection of marine species, Navy
stewardship, and general observation
information including more detailed
information for spotting marine
mammals. Marine mammal observer
training will be provided before active
sonar testing begins.
Marine observers would be aware of
the specific actions to be taken based on
the RDT&E platform if a marine
mammal is observed. Specifically, the
following requirements for personnel
training would apply:
• All marine observers onboard
platforms involved in the Q–20 sonar
test activities will review the NMFSapproved MSAT material prior to use of
active sonar.
• Marine Observers shall be trained
in marine mammal recognition. Marine
Observer training shall include
completion of the Marine Species
Awareness Training, instruction on
governing laws and policies, and
overview of the specific Gulf of Mexico
species present, and observer roles and
responsibilities.
• Marine observers will be trained in
the most effective means to ensure quick
and effective communication within the
command structure in order to facilitate
implementation of mitigation measures
if marine species are spotted.
Range Operating Procedures
The following procedures would be
implemented to maximize the ability of
Navy personnel to recognize instances
when marine mammals are in the
vicinity.
(1) Observer Responsibilities
• Marine observers will have at least
one set of binoculars available for each
person to aid in the detection of marine
mammals.
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• Marine observers will scan the
water from the ship to the horizon and
be responsible for all observations in
their sector. In searching the assigned
sector, the lookout will always start at
the forward part of the sector and search
aft (toward the back). To search and
scan, the lookout will hold the
binoculars steady so the horizon is in
the top third of the field of vision and
direct the eyes just below the horizon.
The lookout will scan for approximately
five seconds in as many small steps as
possible across the field seen through
the binoculars. They will search the
entire sector in approximately fivedegree steps, pausing between steps for
approximately five seconds to scan the
field of view. At the end of the sector
search, the glasses will be lowered to
allow the eyes to rest for a few seconds,
and then the lookout will search back
across the sector with the naked eye.
• Observers will be responsible for
informing the Test Director of any
marine mammal that may need to be
avoided, as warranted.
• These procedures would apply as
much as possible during RMMV
operations. When an RMMV is
operating over the horizon, it is
impossible to follow and observe it
during the entire path. An observer will
be located on the support vessel or
platform to observe the area when the
system is undergoing a small track close
to the support platform.
(2) Operating Procedures
• Test Directors will, as appropriate
to the event, make use of marine species
detection cues and information to limit
interaction with marine species to the
maximum extent possible, consistent
with the safety of the ship.
• During Q–20 sonar activities,
personnel will utilize all available
sensor and optical system (such as Night
Vision Goggles) to aid in the detection
of marine mammals.
• Navy aircraft participating will
conduct and maintain, when
operationally feasible, required, 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.
• Marine mammal detections by
aircraft will be immediately reported to
the Test Director. This action will occur
when it is reasonable to conclude that
the course of the ship will likely close
the distance between the ship and the
detected marine mammal.
• Exclusion Zones—The Navy will
ensure that sonar transmissions are
ceased if any detected marine mammals
are within 200 yards (183 m) of the
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sonar source. Active sonar will not
resume until the marine mammal has
been seen to leave the area, has not been
detected for 30 minutes, or the vessel
has transited more than 2,000 yards
(1,828 m) beyond the location of the last
detection.
• Special conditions applicable for
dolphins only: If, after conducting an
initial maneuver to avoid close quarters
with dolphins, the Test Director or the
Test Director’s designee concludes that
dolphins are deliberately closing to ride
the vessel’s bow wave, no further
mitigation actions are necessary while
the dolphins or porpoises continue to
exhibit bow wave riding behavior.
• Sonar levels (generally)—Navy will
operate sonar at the lowest practicable
level, except as required to meet testing
objectives.
Clearance Procedures
When the test platform (surface vessel
or aircraft) arrives at the test site, an
initial evaluation of environmental
suitability will be made. This evaluation
will include an assessment of sea state
and verification that the area is clear of
visually detectable marine mammals
and indicators of their presence. For
example, large flocks of birds and large
schools of fish are considered indicators
of potential marine mammal presence.
If the initial evaluation indicates that
the area is clear, visual surveying will
begin. The area will be visually
surveyed for the presence of protected
species and protected species
indicators. Visual surveys will be
conducted from the test platform before
test activities begin. When the platform
is a surface vessel, no additional aerial
surveys will be required. For surveys
requiring only surface vessels, aerial
surveys may be opportunistically
conducted by aircraft participating in
the test.
Shipboard monitoring will be staged
from the highest point possible on the
vessel. The observer(s) will be
experienced in shipboard surveys,
familiar with the marine life of the area,
and equipped with binoculars of
sufficient magnification. Each observer
will be provided with a two-way radio
that will be dedicated to the survey, and
will have direct radio contact with the
Test Director. Observers will report to
the Test Director any sightings of marine
mammals or indicators of these species,
as described previously. Distance and
bearing will be provided when
available. Observers may recommend a
‘‘Go’’/‘‘No Go’’ decision, but the final
decision will be the responsibility of the
Test Director.
Post-mission surveys will be
conducted from the surface vessel(s)
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and aircraft used for pre-test surveys.
Any affected marine species will be
documented and reported to NMFS. The
report will include the date, time,
location, test activities, species (to the
lowest taxonomic level possible),
behavior, and number of animals.
NMFS has carefully evaluated the
Navy’s proposed mitigation measures
and considered a 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 measure is
expected to minimize adverse impacts
to marine mammals
• The proven or likely efficacy of the
specific measure to minimize adverse
impacts as planned; and
• The practicability of the measure
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, we have
preliminarily determined that the
proposed mitigation measures provide
the 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.
Proposed Monitoring Measures
In order to issue an ITA for an
activity, section 101(a)(5)(D) of the
MMPA states that 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.
The RDT&E Monitoring Program,
proposed by the Navy as part of its IHA
application, is focused on mitigationbased monitoring. Main monitoring
techniques include use of civilian
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personnel as marine mammal observers
during pre-, during, and post-, test
events.
Systematic monitoring of the affected
area for marine mammals will be
conducted prior to, during, and after test
events using aerial and/or ship-based
visual surveys. Observers will record
information during the test activity.
Data recorded will include exercise
information (time, date, and location)
and marine mammal and/or indicator
presence, species, number of animals,
their behavior, and whether there are
changes in the behavior. Personnel will
immediately report observed stranded
or injured marine mammals to NMFS
stranding response network and NMFS
Regional Office. Reporting requirements
will be included in the Naval Surface
Warfare Center Panama City Division
(NSWC PCD) Mission Activities Final
Environmental Impact Statement/
Overseas Environmental Impact
Statement Annual Activity report as
required by its Final Rule (DON, 2009;
NMFS, 2010d).
Ongoing Monitoring
The Navy has an existing Monitoring
Plan that provides for site-specific
monitoring for MMPA and Endangered
Species Act (ESA) listed species,
primarily marine mammals within the
Gulf of Mexico, including marine water
areas of the Q–20 Study Area (DON,
2009; NMFS, 2010d). This monitoring
plan was initially developed in support
of the NSWC PCD Mission Activities
Final Environmental Impact Statement/
Overseas Environmental Impact
Statement and subsequent Final Rule by
NMFS (DON, 2009; NMFS, 2010d). The
primary goals of monitoring are to
evaluate trends in marine species
distribution and abundance in order to
assess potential population effects from
Navy training and testing events and
determine the effectiveness of the
Navy’s mitigation measures. The
monitoring plan, adjusted annually in
consultation with NMFS, includes
aerial- and ship-based visual
observations, acoustic monitoring, and
other efforts such as oceanographic
observations.
Estimated Take by Incidental
Harassment
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
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12023
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].
Level B Harassment
Of the potential effects that were
described in the Potential Effects of
Exposure of Marine Mammals to Sonar
section, 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 active sonar
exposure, is considered Level B
Harassment. Some of the lower level
physiological stress responses will 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.
In the effects section above, we
described the Southall et al., (2007)
severity scaling system and listed some
examples of the three broad categories
of behaviors: (0–3: Minor and/or brief
behaviors); 4–6 (Behaviors with higher
potential to affect foraging,
reproduction, or survival); 7–9
(Behaviors considered likely to affect
the aforementioned vital rates).
Generally speaking, MMPA Level B
Harassment, as defined in this
document, would include the behaviors
described in the 7–9 category, and a
subset, dependent on context and other
considerations, of the behaviors
described in the 4–6 categories.
Behavioral harassment generally does
not include behaviors ranked 0–3 in
Southall et al., (2007).
Acoustic Masking and
Communication Impairment—Acoustic
masking is considered Level B
Harassment as it can disrupt natural
behavioral patterns by interrupting or
limiting the marine mammal’s receipt or
transmittal of important information or
environmental cues.
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
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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
Navy sonar) as Level B Harassment, not
Level A Harassment (injury).
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Level A Harassment
Of the potential effects that were
described in the Potential Effects of
Exposure of Marine Mammal to Sonar
section, following are the types of
effects that fall into the Level A
Harassment category:
PTS—PTS (resulting from exposure to
active sonar) 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 results
in changes in the chemical composition
of the inner ear fluids.
Acoustic Take Criteria
For the purposes of an MMPA
incidental take 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
military sonar cannot be detected or
measured, 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 uses acoustic criteria that
estimate at what received level (when
exposed to Navy sonar) Level B
Harassment and Level A Harassment of
marine mammals would occur. These
acoustic criteria are discussed below.
Relatively few applicable data exist to
support acoustic criteria specifically for
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HFAS (such as the Q–20 active sonar).
However, because MFAS systems have
larger impact ranges, NMFS will apply
the criteria developed for the MFAS
systems to the HFAS systems.
NMFS utilizes three acoustic criteria
for HFAS/MFAS: PTS (injury—Level A
Harassment), behavioral harassment
from TTS, and sub-TTS (Level B
Harassment). Because the TTS and PTS
criteria are derived similarly and the
PTS criteria was extrapolated from the
TTS data, the TTS and PTS acoustic
criteria will be presented first, before
the behavioral criteria.
For more information regarding these
criteria, please see the Navy’s FEIS for
the NSWC PCD (Navy 2009).
Level B Harassment Threshold (TTS)
As mentioned above, 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 is likely
to occur are 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. NMFS also uses an acoustic
criteria to estimate the number of
marine mammals that might sustain
TTS incidental to a specific activity (in
addition to the behavioral criteria).
A number of investigators have
measured TTS in marine mammals.
These studies measured hearing
thresholds in trained marine mammals
before and after exposure to intense
sounds. The existing cetacean TTS data
are summarized in the following bullets.
• Schlundt et al. (2000) reported the
results of TTS experiments conducted
with 5 bottlenose dolphins and 2
belugas exposed to 1-second tones. This
paper also includes a reanalysis of
preliminary TTS data released in a
technical report by Ridgway et al.
(1997). At frequencies of 3, 10, and 20
kHz, sound pressure levels (SPLs)
necessary to induce measurable
amounts (6 dB or more) of TTS were
between 192 and 201 dB re 1 mPa (EL
= 192 to 201 dB re 1 mPa2-s). The mean
exposure SPL and EL for onset-TTS
were 195 dB re 1 mPa and 195 dB re 1
mPa2-s, respectively.
• Finneran et al. (2001, 2003, 2005)
described TTS experiments conducted
with bottlenose dolphins exposed to 3kHz tones with durations of 1, 2, 4, and
8 seconds. Small amounts of TTS (3 to
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6 dB) were observed in one dolphin
after exposure to ELs between 190 and
204 dB re 1 microPa2-s. These results
were consistent with the data of
Schlundt et al. (2000) and showed that
the Schlundt et al. (2000) data were not
significantly affected by the masking
sound used. These results also
confirmed that, for tones with different
durations, the amount of TTS is best
correlated with the exposure EL rather
than the exposure SPL.
• Nachtigall et al. (2003) measured
TTS in a bottlenose dolphin exposed to
octave-band sound centered at 7.5 kHz.
Nachtigall et al. (2003a) reported TTSs
of about 11 dB measured 10 to 15
minutes after exposure to 30 to 50
minutes of sound with SPL 179 dB re
1 mPa (EL about 213 dB re mPa2-s). No
TTS was observed after exposure to the
same sound at 165 and 171 dB re 1 mPa.
Nachtigall et al. (2004) reported TTSs of
around 4 to 8 dB 5 minutes after
exposure to 30 to 50 minutes of sound
with SPL 160 dB re 1 mPa (EL about 193
to 195 dB re 1 mPa 2-s). The difference
in results was attributed to faster post
exposure threshold measurement—TTS
may have recovered before being
detected by Nachtigall et al. (2003).
These studies showed that, for long
duration exposures, lower sound
pressures are required to induce TTS
than are required for short-duration
tones.
• Finneran et al. (2000, 2002)
conducted TTS experiments with
dolphins and belugas exposed to
impulsive sounds similar to those
produced by distant underwater
explosions and seismic waterguns.
These studies showed that, for very
short-duration impulsive sounds, higher
sound pressures were required to
induce TTS than for longer-duration
tones.
Some of the more important data
obtained from these studies are onsetTTS levels (exposure levels sufficient to
cause a just-measurable amount of TTS)
often defined as 6 dB of TTS (for
example, Schlundt et al., 2000) and the
fact that energy metrics (sound exposure
levels (SEL), which include a duration
component) better predict when an
animal will sustain TTS than pressure
(SPL) alone. NMFS’ TTS criteria (which
indicate the received level at which
onset TTS (>6dB) is induced) for HFAS/
MFAS are as follows:
• Cetaceans—195 dB re 1 mPa 2-s
(based on mid-frequency cetaceans—no
published data exist on auditory effects
of noise in low or high frequency
cetaceans) (Southall et al., 2007).
A detailed description of how TTS
criteria were derived from the results of
the above studies may be found in
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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 the 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
discovered through study of terrestrial
mammals. NMFS uses the following
acoustic criteria for injury:
• Cetaceans—215 dB re 1 mPa2-s
(based on mid-frequency cetaceans—no
published data exist on auditory effects
of noise in low or high frequency
cetaceans) (Southall et al., 2007).
These criteria are based on a 20 dB
increase in SEL over that required for
onset-TTS. Extrapolations from
terrestrial mammal data indicate that
PTS occurs at 40 dB or more of TS, and
that TS growth occurs at a rate of
approximately 1.6 dB TS per dB
increase in EL. There is a 34-dB TS
difference between onset-TTS (6 dB)
and onset-PTS (40 dB). Therefore, an
animal would require approximately 20dB of additional exposure (34 dB
divided by 1.6 dB) above onset-TTS to
reach PTS. A detailed description of
how TTS criteria were derived from the
results of the above studies may be
found in Chapter 3 of Southall et al.
(2007), as well as the Navy’s NSWC PCD
LOA application. Southall et al. (2007)
recommend a precautionary dual
criteria for TTS (230 dB re 1 mPa (SPL)
in addition to 215 re 1 mPa2-s (SEL)) to
account for the potentially damaging
transients embedded within non-pulse
exposures. However, in the case of
HFAS/MFAS, the distance at which an
animal would receive 215 (SEL) is
farther from the source than the distance
at which they would receive 230 (SPL)
and therefore, it is not necessary to
consider 230 dB.
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
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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.
Level B Harassment Risk Function
(Behavioral Harassment)
The first MMPA authorization for take
of marine mammals incidental to
tactical active sonar was issued in 2006
for Navy Rim of the Pacific training
exercises in Hawaii. 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 does not support
the use of a step function to estimate
behavioral harassment.
Unlike step functions, acoustic risk
continuum functions (which are also
called ‘‘exposure-response functions,’’
‘‘dose-response functions,’’ or ‘‘stress
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. The Navy and
NMFS have previously used acoustic
risk functions to estimate the probable
responses of marine mammals to
acoustic exposures in the Navy FEISs on
the SURTASS LFA sonar (DoN, 2001c)
and the North Pacific Acoustic
Laboratory experiments conducted off
the Island of Kauai (ONR, 2001). The
specific risk functions used here were
also used in the MMPA regulations and
FEIS for Hawaii Range Complex (HRC),
Southern California Range Complex
(SOCAL), and Atlantic Fleet Active
Sonar Testing (AFAST). As discussed in
the Effects section, factors other than
received level (such as distance from or
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bearing to the sound source) can affect
the way that marine mammals respond;
however, data to support a quantitative
analysis of those (and other factors) do
not currently exist. NMFS will continue
to modify these criteria as new data
becomes available.
To assess the potential effects on
marine mammals associated with active
sonar used during training activity, the
Navy and NMFS applied a risk function
that estimates the probability of
behavioral responses that NMFS would
classify as harassment for the purposes
of the MMPA given exposure to specific
received levels of MFA sonar. The
mathematical function is derived from a
solution in Feller (1968) as defined in
the SURTASS LFA Sonar Final OEIS/
EIS (DoN, 2001), and relied on in the
Supplemental SURTASS LFA Sonar EIS
(DoN, 2007a) for the probability of MFA
sonar risk for MMPA Level B behavioral
harassment with input parameters
modified by NMFS for MFA sonar for
mysticetes and odontocetes (NMFS,
2008). The same risk function and input
parameters will be applied to high
frequency active (HFA) (≤10 kHz)
sources until applicable data becomes
available for high frequency sources.
In order to represent a probability of
risk, the function should have a value
near zero at very low exposures, and a
value near one for very high exposures.
One class of functions that satisfies this
criterion is cumulative probability
distributions, a type of cumulative
distribution function. In selecting a
particular functional expression for risk,
several criteria were identified:
• The function must use parameters
to focus discussion on areas of
uncertainty;
• The function should contain a
limited number of parameters;
• The function should be capable of
accurately fitting experimental data; and
• The function should be reasonably
convenient for algebraic manipulations.
As described in U.S. Department of
the Navy (2001), the mathematical
function below is adapted from a
solution in Feller (1968).
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
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Chapter 3 of Southall et al. (2007), as
well as the Navy’s Q–20 IHA
application.
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A = Risk transition sharpness parameter =
10 (odontocetes) or 8 (mysticetes)
In order to use this function to
estimate the percentage of an exposed
population that would respond in a
manner that NMFS classifies as Level B
harassment, based on a given received
level, the values for B, K and A need to
be identified.
B Parameter (Basement)—The B
parameter is the estimated received
level below which the probability of
disruption of natural behavioral
patterns, such as migration, surfacing,
nursing, breeding, feeding, or sheltering,
to a point where such behavioral
patterns are abandoned or significantly
altered approaches zero for the HFAS/
MFAS risk assessment. At this received
level, the curve would predict that the
percentage of the exposed population
that would be taken by Level B
Harassment approaches zero. For HFAS/
MFAS, NMFS has determined that B =
120 dB. This level is based on a broad
overview of the levels at which many
species have been reported responding
to a variety of sound sources.
K Parameter (representing the 50
percent Risk Point)—The K parameter is
based on the received level that
corresponds to 50 percent risk, or the
received level at which we believe 50
percent of the animals exposed to the
designated received level will respond
in a manner that NMFS classifies as
Level B Harassment. The K parameter (K
= 45 dB) is based on three datasets in
which marine mammals exposed to
mid-frequency sound sources were
reported to respond in a manner that
NMFS would classify as Level B
Harassment. There is widespread
consensus that marine mammal
responses to HFA/MFA sound signals
need to be better defined using
controlled exposure experiments (Cox et
al., 2006; Southall et al., 2007). The
Navy is contributing to an ongoing
behavioral response study in the
Bahamas that is expected to provide
some initial information on beaked
whales, the species identified as the
most sensitive to MFAS. NMFS is
leading this international effort with
scientists from various academic
institutions and research organizations
to conduct studies on how marine
mammals respond to underwater sound
exposures. Until additional data is
available, however, NMFS and the Navy
have determined that the following
three data sets are most applicable for
the direct use in establishing the K
parameter for the HFAS/MFAS risk
function. These data sets, summarized
below, represent the only known data
that specifically relate altered
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behavioral responses (that NMFS would
consider Level B Harassment) to
exposure to HFAS/MFAS sources.
Even though these data are considered
the most representative of the proposed
specified activities, and therefore the
most appropriate on which to base the
K parameter (which basically
determines the midpoint) of the risk
function, these data have limitations,
which are discussed in Appendix J of
the Navy’s EIS for the NSWC PCD (DoN,
2009) and summarized in the Navy’s
IHA application.
Calculation of K Paramenter—NMFS
and the Navy used the mean of the
following values to define the midpoint
of the function: (1) The mean of the
lowest received levels (185.3 dB) at
which individuals responded with
altered behavior to 3 kHz tones in the
SSC data set; (2) the estimated mean
received level value of 169.3 dB
produced by the reconstruction of the
USS SHOUP incident in which killer
whales exposed to MFA sonar (range
modeled possible received levels: 150 to
180 dB); and (3) the mean of the 5
maximum received levels at which
Nowacek et al. (2004) observed
significantly altered responses of right
whales to the alert stimuli than to the
control (no input signal) is 139.2 dB
SPL. The arithmetic mean of these three
mean values is 165 dB SPL. The value
of K is the difference between the value
of B (120 dB SPL) and the 50 percent
value of 165 dB SPL; therefore, K = 45.
A Parameter (Steepness)—NMFS
determined that a steepness parameter
(A) = 10 is appropriate for odontocetes
(except harbor porpoises) and pinnipeds
and A = 8 is appropriate for mysticetes.
The use of a steepness parameter of A
= 10 for odontocetes (except harbor
porpoises) for the HFAS/MFAS risk
function was based on the use of the
same value for the SURTASS LFA risk
continuum, which was supported by a
sensitivity analysis of the parameter
presented in Appendix D of the
SURTASS/LFA FEIS (DoN, 2001c). As
concluded in the SURTASS FEIS/EIS,
the value of A = 10 produces a curve
that has a more gradual transition than
the curves developed by the analyses of
migratory gray whale studies (Malme et
al., 1984; Buck and Tyack, 2000; and
SURTASS LFA Sonar EIS, Subchapters
1.43, 4.2.4.3 and Appendix D, and
NMFS, 2008).
NMFS determined that a lower
steepness parameter (A = 8), resulting in
a shallower curve, was appropriate for
use with mysticetes and HFAS/MFAS.
The Nowacek et al. (2004) dataset
contains the only data illustrating
mysticete behavioral responses to a midfrequency sound source. A shallower
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curve (achieved by using A = 8) better
reflects the risk of behavioral response
at the relatively low received levels at
which behavioral responses of right
whales were reported in the Nowacek et
al. (2004) data. Compared to the
odontocete curve, this adjustment
results in an increase in the proportion
of the exposed population of mysticetes
being classified as behaviorally harassed
at lower RLs, such as those reported in
and supported by the only dataset
currently available.
Basic Application of the Risk
Function—The risk function is used to
estimate the percentage of an exposed
population that is likely to exhibit
behaviors that would qualify as
harassment (as that term is defined by
the MMPA applicable to military
readiness activities, such as the Navy’s
testing and research activities with
HFA/MFA sonar) at a given received
level of sound. For example, at 165 dB
SPL (dB re: 1 mPa rms), the risk (or
probability) of harassment is defined
according to this function as 50 percent,
and Navy/NMFS applies that by
estimating that 50 percent of the
individuals exposed at that received
level are likely to respond by exhibiting
behavior that NMFS would classify as
behavioral harassment. The risk
function is not applied to individual
animals, only to exposed populations.
The data primarily used to produce
the risk function (the K parameter) were
compiled from four species that had
been exposed to sound sources in a
variety of different circumstances. As a
result, the risk function represents a
general relationship between acoustic
exposures and behavioral responses that
is then applied to specific
circumstances. That is, the risk function
represents a relationship that is deemed
to be generally true, based on the
limited, best-available science, but may
not be true in specific circumstances. In
particular, the risk function, as currently
derived, treats the received level as the
only variable that is relevant to a marine
mammal’s behavioral response.
However, we know that many other
variables—the marine mammal’s
gender, age, and prior experience; the
activity it is engaged in during an
exposure event, its distance from a
sound source, the number of sound
sources, and whether the sound sources
are approaching or moving away from
the animal—can be critically important
in determining whether and how a
marine mammal will respond to a sound
source (Southall et al., 2007). The data
that are currently available do not allow
for incorporation of these other
variables in the current risk functions;
however, the risk function represents
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12027
the best use of the data that are available
(Figure 1).
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As more specific and applicable data
become available for HFAS/MFAS
sources, NMFS can use these data to
modify the outputs generated by the risk
function to make them more realistic.
Ultimately, data may exist to justify the
use of additional, alternate, or
multivariate functions. For example, as
mentioned previously, the distance from
the sound source and whether it is
perceived as approaching or moving
away can affect the way an animal
responds to a sound (Wartzok et al.,
2003).
Estimated Exposures of Marine
Mammals
Acoustical modeling provides an
estimate of the actual exposures.
Detailed information and formulas to
model the effects of sonar from Q–20
sonar testing activities in the Q–20
Study Area are provided in Appendix
A, Supplemental Information for
Underwater Noise Analysis of the
Navy’s IHA application.
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The quantitative analysis was based
on conducting sonar operations in 13
different geographical regions, or
provinces. Using combined marine
mammal density and depth estimates,
which are detailed later in this section,
acoustical modeling was conducted to
calculate the actual exposures. Refer to
Appendix B, Geographic Description of
Environmental Provinces of the Navy’s
IHA application, for additional
information on provinces. Refer to
Appendix C, Definitions and Metrics for
Acoustic Quantities of the Navy’s IHA
application, for additional information
regarding the acoustical analysis.
The approach for estimating potential
acoustic effects from Q–20 test activities
on cetacean species uses the
methodology that the DON developed in
cooperation with NMFS for the Navy’s
HRC Draft EIS (DON, 2007c). The
exposure analysis for behavioral
response to sound in the water uses
energy flux density for Level A
harassment and the methods for risk
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function for Level B harassment
(behavioral). The methodology is
provided here to determine the number
and species of marine mammals for
which incidental take authorization is
requested.
To estimate acoustic effects from the
Q–20 test activities, acoustic sources to
be used were examined with regard to
their operational characteristics as
described in the previous section.
Systems with an operating frequency
greater than 200 kHz were not analyzed
in the detailed modeling as these signals
attenuate rapidly resulting in very short
propagation distances. Based on the
information above, the Navy modeled
the Q–20 sonar parameters including
source levels, ping length, the interval
between pings, output frequencies,
directivity (or angle), and other
characteristics based on records from
previous test scenarios and projected
future testing. Additional information
on sonar systems and their associated
parameters is in Appendix A,
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Supplemental Information for
Underwater Noise Analysis of the
Navy’s IHA application.
Every active sonar operation includes
the potential to expose marine animals
in the neighboring waters. The number
of animals exposed to the sonar is
dictated by the propagation field and
the manner in which the sonar is
operated (i.e., source level, depth,
frequency, pulse length, directivity,
platform speed, repetition rate). The
modeling for Q–20 test activities
involving sonar occurred in five broad
steps listed below, and was conducted
based on the typical RDT&E activities
planned for the Q–20 Study Area.
1. Environmental Provinces: The Q–
20 Study Area is divided into 13
environmental provinces, and each has
a unique combination of environmental
conditions. These represent various
combinations of eight bathymetry
provinces, one Sound Velocity Profile
(SVP) province, and three LowFrequency Bottom Loss geo-acoustic
provinces and two High-Frequency
Bottom Loss classes. These are
addressed by defining eight
fundamental environments in two
seasons that span the variety of depths,
bottom types, sound speed profiles, and
sediment thicknesses found in the Q–20
Study Area. The two seasons encompass
winter and summer, which are the two
extremes for the GOM, the acoustic
propagation characteristics do not vary
significantly between the two. Each
marine modeling area can be
quantitatively described as a unique
combination of these environments.
2. Transmission Loss: Since sound
propagates differently in these
environments, separate transmission
loss calculations must be made for each,
in both seasons. The transmission loss
is predicted using Comprehensive
Acoustic Simulation System/Gaussian
Ray Bundle (CASS–GRAB) sound
modeling software.
3. Exposure Volumes: The
transmission loss, combined with the
source characteristics, gives the energy
field of a single ping. The energy of
more than 10 hours of pinging is
summed, carefully accounting for
overlap of several pings, so an accurate
average exposure of an hour of pinging
is calculated for each depth increment.
At more than 10 hours, the source is too
far away and the energy is negligible.
Repeating this calculation for each
environment in each season gives the
hourly ensonified volume, by depth, for
each environment and season. This step
begins the method for risk function
modeling.
4. Marine Mammal Densities: The
marine mammal densities were given in
two dimensions, but using reliable peerreviewed literature sources (published
literature and agency reports) described
in the following subsection, the depth
regimes of these marine mammals are
used to project the two dimensional
densities (expressed as the number of
animals per area where all individuals
are assumed to be at the water’s surface)
into three dimensions (a volumetric
approach whereby two-dimensional
animal density incorporates depth into
the calculation estimates).
5. Exposure Calculations: Each marine
mammal’s three-dimensional (3–D)
density is multiplied by the calculated
impact volume to that marine mammal
depth regime. This value is the number
of exposures per hour for that particular
marine mammal. In this way, each
marine mammal’s exposure count per
hour is based on its density, depth
habitat, and the ensonified volume by
depth.
The planned sonar hours were
inserted and a cumulative number of
exposures was determined for the
proposed action.
Based on the analysis, Q–20 sonar
operations in non-territorial waters may
expose up to six species to sound likely
to result in Level B (behavioral)
harassment (Table 2). They include the
bottlenose dolphin (Tursiops truncatus),
Atlantic spotted dolphin (Stenella
frontalis), pantropical spotted dolphin
(Stenella attenuata), striped dolphin
(Stenella coeruleoalba), spinner dolphin
(Stenella longirostris), and Clymene
dolphin (Stenella clymene). No marine
mammals would be exposed to levels of
sound likely to result in TTS. The Navy
requests that the take numbers of marine
mammals for its IHA reflect the
exposure numbers listed in Table 2.
TABLE 2—ESTIMATES OF MARINE MAMMAL EXPOSURES FROM SONAR IN NON-TERRITORIAL WATERS PER YEAR
Marine mammal species
Bottlenose dolphin (GOM oceanic) .............................................................................................
Pantropical spotted dolphin .........................................................................................................
Atlantic spotted dolphin ...............................................................................................................
Spinner dolphin ............................................................................................................................
Clymene dolphin ..........................................................................................................................
Striped dolphin .............................................................................................................................
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Potential for Long-Term Effects
Q–20 test activities will be conducted
in the same general areas, so marine
mammal populations could be exposed
to repeated activities over time.
However, as described earlier, this
analysis assumes that short-term noninjurious SELs predicted to cause
temporary behavioral disruptions
qualify as Level B harassment. It is
highly unlikely that behavioral
disruptions will result in any long-term
significant effects.
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Potential for Effects on ESA-Listed
Species
To further examine the possibility of
whale exposures from the proposed
testing, CASSGRAB sound modeling
software was used to estimate
transmission losses and received sound
pressure levels (SPLs) from the Q–20
when operating in the test area.
Specifically, four radials out towards
DeSoto Canyon (which is considered an
important habitat for the ESA-listed
sperm whales) were calculated. The
results indicate the relatively rapid
attenuation of sound pressure levels
with distance from the source, which is
not surprising given the high frequency
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(TTS)
Level A
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0
0
0
0
0
0
Level B
(behavioral)
0
0
0
0
0
0
399
126
315
126
42
42
of the source. Below 120 dB, the risk of
significant change in a biologically
important behavior approaches zero.
This threshold is reached at a distance
of only 2.8 km (1.5 nm) from the source.
With the density of sperm whales being
near zero in this potential zone of
influence, this calculation reinforces
NMFS’ conclusion that the proposed
activity is not likely to result in the take
of sperm whales. It should also be noted
that DeSoto Canyon is well beyond the
distance at which sound pressure levels
from the Q–20 attenuate to zero.
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Negligible Impact and Small Numbers
Analysis and Determination
Pursuant to NMFS’ regulations
implementing the MMPA, an applicant
is required to estimate the number of
animals that will be ‘‘taken’’ by the
specified activities (i.e., takes by
harassment only, or takes by
harassment, injury, and/or death). This
estimate informs the analysis that NMFS
must perform to determine whether the
activity will have a ‘‘negligible impact’’
on the species or stock. Level B
(behavioral) harassment occurs at the
level of the individual(s) and does not
assume any resulting population-level
consequences, though there are known
avenues through which behavioral
disturbance of individuals can result in
population-level effects. 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 Level B harassment takes, alone, is
not enough information on which to
base an impact determination. In
addition to considering estimates of the
number of marine mammals that might
be ‘‘taken’’ through behavioral
harassment, 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.), or any of the other
variables mentioned in the first
paragraph (if known), as well as the
number and nature of estimated Level A
takes, the number of estimated
mortalities, and effects on habitat.
The Navy’s specified activities have
been described based on best estimates
of the number of Q–20 sonar test hours
that the Navy will conduct. Taking the
above into account, considering the
sections discussed below, and
dependent upon the implementation of
the proposed mitigation measures,
NMFS has preliminarily determined
that Navy’s Q–20 sonar test activities in
the non-territorial waters will have a
negligible impact on the marine
mammal species and stocks present in
the Q–20 Study Area.
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Behavioral Harassment
As discussed in the Potential Effects
of Exposure of Marine Mammals to
Sonar section and illustrated in the
conceptual framework, marine
mammals can respond to HFAS/MFAS
in many different ways, a subset of
which qualifies as harassment. One
thing that the take estimates do not take
into account is the fact that most marine
mammals will likely avoid strong sound
sources to one extent or another.
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Although an animal that avoids the
sound source will likely still be taken in
some instances (such as if the avoidance
results in a missed opportunity to feed,
interruption of reproductive behaviors,
etc.), in other cases avoidance may
result in fewer instances of take than
were estimated or in the takes resulting
from exposure to a lower received level
than was estimated, which could result
in a less severe response. The Navy
proposes only 420 hours of highfrequency sonar operations per year for
the Q–20 sonar testing activities, spread
among 42 days with an average of 10
hours per day, in the Q–20 Study Area.
There will be no powerful tactical midfrequency sonar involved. Therefore,
there will be no disturbance to marine
mammals resulting from MFAS systems
(such as 53C). The effects that might be
expected from the Navy’s major training
exercises at the Atlantic Fleet Active
Sonar Training (AFAST) Range, Hawaii
Range Complex (HRC), and Southern
California (SOCAL) Range Complex will
not occur here. The source level of the
Q–20 sonar is much lower than the 53C
series MFAS system, and high
frequency signals tend to have more
attenuation in the water column and are
more prone to lose their energy during
propagation. Therefore, their zones of
influence are much smaller, thereby
making it easier to detect marine
mammals and prevent adverse effects
from occurring.
The Navy has been conducting
monitoring activities since 2006 on its
sonar operations in a variety of the
Naval range complexes (e.g., AFAST,
HRC, SOCAL) under the Navy’s own
protective measures and under the
regulations and LOAs. Monitoring
reports based on these major training
exercises using military sonar have
shown that no marine mammal injury or
mortality has occurred as a result of the
sonar operations (DoN, 2011a; 2011b).
Diel Cycle
As noted previously, many animals
perform vital functions, such as feeding,
resting, traveling, and socializing on a
diel cycle (24-hr 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
one day and not recurring on
subsequent days is not considered
particularly severe unless it could
directly affect reproduction or survival
(Southall et al., 2007).
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In the previous section, we discussed
the fact that potential behavioral
responses to HFAS/MFAS that fall into
the category of harassment could range
in severity. By definition, the takes by
behavioral harassment involve the
disturbance of a marine mammal or
marine mammal stock in the wild by
causing disruption of natural behavioral
patterns (such as migration, surfacing,
nursing, breeding, feeding, or sheltering)
to a point where such behavioral
patterns are abandoned or significantly
altered. In addition, the amount of time
the Q–20 sonar testing will occur is 420
hours per year in non-territorial waters,
and is spread among 42 days with an
average of 10 hours per day. Thus the
exposure is expected to be sporadic
throughout the year and is localized
within a specific testing site.
TTS
Based on the Navy’s model and NMFS
analysis, it is unlikely that marine
mammals would be exposed to sonar
received levels that could cause TTS
due to the lower source level (207–212
dB re 1 mPa at 1 m) and high attenuation
rate of the HAFS signals (above 35 kHz).
Acoustic Masking or Communication
Impairment
As discussed above, it is possible that
anthropogenic sound could result in
masking of marine mammal
communication and navigation signals.
However, masking only occurs during
the time of the signal (and potential
secondary arrivals of indirect rays),
versus TTS, which occurs continuously
for its duration. The Q–20 ping duration
is in milliseconds and the system is
relatively low-powered making its range
of effect smaller. Therefore, masking
effects from the Q–20 sonar signals are
expected to be minimal. If masking or
communication impairment were to
occur briefly, it would be in the
frequency range of above 35 kHz (the
lower limit of the Q–20 signals), which
overlaps with some marine mammal
vocalizations; however, it would likely
not mask the entirety of any particular
vocalization or communication series
because the pulse length, frequency, and
duty cycle of the Q–20 sonar signal does
not perfectly mimic the characteristics
of any marine mammal’s vocalizations.
PTS, Injury, or Mortality
Based on the Navy’s model and NMFS
analysis, it is unlikely that PTS, injury,
or mortality of marine mammals would
occur from the proposed Q–20 sonar
testing activities. As discussed earlier,
the lower source level (207–212 dB re 1
mPa at 1 m) and high attenuation rate of
the HFAS signals (above 35 kHz) make
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it highly unlikely that any marine
mammals in the vicinity would be
injured (including PTS) or killed as a
result of sonar exposure.
Based on the aforementioned
assessment, NMFS determines that
approximately 399 bottlenose dolphins,
126 pantropical spotted dolphins, 315
Atlantic spotted dolphins, 126 spinner
dolphins, 42 Clymene dolphins, and 42
striped dolphins would be affected by
Level B behavioral harassment as a
result of the proposed Q–20 sonar
testing activities. These numbers
represent approximately 10.76%,
0.37%, 1.26%, 6.33%, and 0.64% of
bottlenose dolphins (GOM oceanic
stock), pantropical spotted dolphins,
striped dolphins, spinner dolphins, and
Clymene dolphins, respectively, of these
species in the GOM region (calculation
based on NMFS 2011 US Atlantic and
Gulf of Mexico Marine Mammal Stock
Assessment). The percentage of
potentially affected Atlantic spotted
dolphin is unknown since there is no
current population assessment of this
species in the Gulf of Mexico region.
However, based on the most recent
abundance estimate published in NMFS
Atlantic and GOM SARs conducted in
the northern Gulf of Mexico outer
continental shelf during fall 2000–2001
and oceanic waters during spring/
summer 2003–2004, the population was
estimated at 37,611 (NMFS 2011). Using
this number, it is estimated that
approximately 0.84% of Atlantic
spotted dolphins would be taken by
Level B behavioral harassment from the
Navy’s proposed sonar test activities.
Based on the supporting analyses,
which suggest that no marine mammals
will be killed, injured, or receive TTS as
a result of the Q–20 sonar testing
activities, and no more than a small
number of any affected species will be
taken in the form of short-term Level B
behavioral harassment. Coupled with
the fact that these impacts will likely
not occur in areas and times critical to
reproduction, NMFS has preliminarily
determined that the taking of these
species as a result of the Navy’s Q–20
sonar test will have a negligible impact
on the marine mammal species and
stocks present in the Q–20 Study Area.
Subsistence Harvest of Marine
Mammals
NMFS has preliminarily determined
that the total taking of marine mammal
species or stocks from the Navy’s Q–20
sonar testing in the Q–20 Study Area
would not have an unmitigable adverse
impact on the availability of the affected
species or stocks for subsistence uses,
since there are no such uses in the
specified area.
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Endangered Species Act (ESA)
Based on the analysis of the Navy
Marine Resources Assessment (MRA)
data on marine mammal distributions,
there is near zero probability that sperm
whale will occur in the vicinity of the
proposed Q–20 test area. No other ESAlisted marine mammal is expected to
occur in the vicinity of the test area. In
addition, acoustic modeling analysis
indicates that none of the ESA-listed
marine mammal species would be
exposed to levels of sound that would
constitute a ‘‘take’’ under the MMPA,
due to the low source level and high
attenuation rates of the Q–20 sonar
signal. Therefore, the Navy has
determined that ESA-listed species are
not likely to be adversely affected as the
result of the Navy’s proposed Q–20
testing activities and has requested
concurrence from NMFS.
National Environmental Policy Act
(NEPA)
In 2009, the Navy prepared a Final
Environmental Impact Statement/
Overseas Environmental Impact
Statement for the NSWC PCD Mission
Activities (FEIS/OEIS), and NMFS
subsequently adopted the FEIS/OEIS for
its rule governing the Navy’s RDT&E
activities in the NSWC PCD Study Area.
The currently proposed Q–20 sonar
testing activities are similar to the sonar
testing activities described in the FEIS/
OEIS for NSWC PCD mission activities.
NMFS will prepare an Environmental
Assessment to reflect these additional
Q–20 sonar test activities.
Commission’s Web site at https://
www.cftc.gov.
CONTACT PERSON FOR MORE INFORMATION:
Sauntia S. Warfield, 202–418–5084.
Sauntia S. Warfield,
Assistant Secretary of the Commission.
[FR Doc. 2012–4853 Filed 2–24–12; 4:15 pm]
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Sunshine Act Meeting Notice
10 a.m., Friday, March
2, 2012.
PLACE: 1155 21st St. NW., Washington,
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Room.
STATUS: Closed.
MATTERS TO BE CONSIDERED:
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Matters. In the event that the times or
dates of these or any future meetings
change, an announcement of the change,
along with the new time and place of
the meeting will be posted on the
Commission’s Web site at https://
www.cftc.gov.
CONTACT PERSON FOR MORE INFORMATION:
Sauntia S. Warfield, 202–418–5084.
TIME AND DATE:
Sauntia S. Warfield,
Assistant Secretary of the Commission.
[FR Doc. 2012–4864 Filed 2–24–12; 4:15 pm]
BILLING CODE 6351–01–P
Dated: February 23, 2012.
James H. Lecky,
Director, Office of Protected Resources,
National Marine Fisheries Service.
COMMODITY FUTURES TRADING
COMMISSION
[FR Doc. 2012–4695 Filed 2–27–12; 8:45 am]
10 a.m., Friday, March
16, 2012.
PLACE: 1155 21st St. NW., Washington,
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Room.
STATUS: Closed.
MATTERS TO BE CONSIDERED:
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Matters. In the event that the times or
dates of these or any future meetings
change, an announcement of the change,
along with the new time and place of
the meeting will be posted on the
Commission’s Web site at https://
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CONTACT PERSON FOR MORE INFORMATION:
Sauntia S. Warfield, 202–418–5084.
BILLING CODE 3510–22–P
COMMODITY FUTURES TRADING
COMMISSION
Notice of Sunshine Act Meetings
Time and Date: 10 a.m., Friday,
March 30, 2012.
PLACE: 1155 21st St. NW., Washington,
DC, 9th Floor Commission Conference
Room.
STATUS: Closed.
DATES:
Matters To Be Considered
Surveillance and Enforcement
Matters. In the event that the times or
dates of these or any future meetings
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PO 00000
Frm 00030
Fmt 4703
Sfmt 9990
Sunshine Act Meeting Notice
TIME AND DATE:
Sauntia S. Warfield,
Assistant Secretary of the Commission.
[FR Doc. 2012–4863 Filed 2–24–12; 4:15 pm]
BILLING CODE 6351–01–P
E:\FR\FM\28FEN1.SGM
28FEN1
Agencies
[Federal Register Volume 77, Number 39 (Tuesday, February 28, 2012)]
[Notices]
[Pages 12010-12030]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-4695]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XA950
Takes of Marine Mammals Incidental to Specified Activities; Navy
Research, Development, Test and Evaluation Activities at the Naval
Surface Warfare Center Panama City Division
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental harassment authorization; request
for comments.
-----------------------------------------------------------------------
SUMMARY: NMFS has received an application from the U.S. Navy (Navy) for
an Incidental Harassment Authorization (IHA) to take marine mammals, by
harassment, incidental to
[[Page 12011]]
conducting research, development, test and evaluation (RDT&E)
activities at the Naval Surface Warfare Center Panama City Division
(NSWC PCD). Pursuant to the Marine Mammal Protection Act (MMPA), NMFS
is requesting comments on its proposal to issue an IHA to the Navy to
incidentally harass, by Level B Harassment only, marine mammals during
the specified activity.
DATES: Comments and information must be received no later than March
29, 2012.
ADDRESSES: Comments on the application should be addressed to Michael
Payne, Chief, Permits and Conservation Division, Office of Protected
Resources, National Marine Fisheries Service, 1315 East-West Highway,
Silver Spring, MD 20910. The mailbox address for providing email
comments is itp.guan@noaa.gov. NMFS is not responsible for email
comments sent to addresses other than the one provided here. Comments
sent via email, including all attachments, must not exceed a 10-
megabyte file size.
Instructions: All comments received are a part of the public record
and will generally be posted to https://www.nmfs.noaa.gov/pr/permits/incidental.htm without change. All Personal Identifying Information
(for example, name, address, etc.) voluntarily submitted by the
commenter may be publicly accessible. Do not submit Confidential
Business Information or otherwise sensitive or protected information.
A copy of the application containing a list of the references used
in this document may be obtained by writing to the address specified
above, telephoning the contact listed below (see FOR FURTHER
INFORMATION CONTACT), or visiting https://www.nmfs.noaa.gov/pr/permits/incidental.htm. Documents cited in this notice may also be viewed, by
appointment, during regular business hours, at the aforementioned
address.
FOR FURTHER INFORMATION CONTACT: Shane Guan, Office of Protected
Resources, NMFS, (301) 427-8401.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the MMPA (16 U.S.C. 1361 et seq.)
direct the Secretary of Commerce (Secretary) 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) if certain findings are made and regulations are
issued or, if the taking is limited to harassment, 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 taking
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 and amended the definition of ``harassment'' as it
applies to a ``military readiness activity'' to read as follows
(Section 3(18)(B) of the MMPA):
(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].
Section 101(a)(5)(D) of the MMPA established an expedited process
by which citizens of the United States can apply for an authorization
to incidentally take small numbers of marine mammals by harassment.
Section 101(a)(5)(D) establishes a 45-day time limit for NMFS review of
an application followed by a 30-day public notice and comment period on
any proposed authorizations for the incidental harassment of marine
mammals. Within 45 days of the close of the comment period, NMFS must
either issue or deny the authorization.
Summary of Request
NMFS received an application on December 28, 2011, from the Navy
for the taking, by harassment, of marine mammals incidental to
conducting testing of the AN/AQS-20A Mine Reconnaissance Sonar System
(hereafter referred to as the Q-20) in the Naval Surface Warfare
Center, Panama City Division (NSWC PCD) testing range in the Gulf of
Mexico (GOM) from April 2012 through April 2013. The Q-20 sonar test
activities are proposed to be conducted in the non-territorial waters
of the United States (beyond 12 nautical miles) in the Gulf of Mexico
(GOM, see Figure 2-1 of the Navy IHA application).
Description of the Specific Activity
The purpose of the Navy's activities is to meet the developmental
testing requirements of the Q-20 system by verifying its performance in
a realistic ocean and threat environment and supporting its integration
with the Remote Multi-Mission Vehicle (RMMV) and ultimately the
Littoral Combat Ship (LCS). Testing would include component, subsystem-
level, and full-scale system testing in an operational environment.
The need for the proposed activities is to support the timely
deployment of the Q-20 to the operational Navy for Mine Countermeasure
(MCM) activities abroad, allowing the Navy to meet its statutory
mission to deploy naval forces equipped and trained to meet existing
and emergent threats worldwide and to enhance its ability to operate
jointly with other components of the armed forces.
The proposed activities are to test the Q-20 from the RMMV and from
surrogate platforms such as a small surface vessel or helicopter. The
RMMV or surrogate platforms will be deployed from the Navy's new LCS or
its surrogates. The Navy is evaluating potential environmental effects
associated with the Q-20 test activities proposed for the Q-20 Study
Area (see below for detailed description of the Study Area), which
includes non-territorial waters of Military Warning Area 151 (W-151;
includes Panama City Operating Area). Q-20 test activities occur at sea
in the waters present within the Q-20 Study Area. No hazardous waste is
generated at sea during Q-20 test activities. There are two components
associated with the Q-20 test activities, which are addressed below.
Surface Operations
A significant portion of Q-20 test activities rely on surface
operations to successfully complete the missions. The Proposed Action
includes up to 420 hours of surface operations during active sonar
testing per year in the Q-20 Study Area. Other surface operations occur
when sonar is not active. Three subcategories make up surface
operations: support activities; tows; and deployment and recovery of
equipment. Testing requiring surface operations may include a single
test event (one day
[[Page 12012]]
of activity) or a series of test events spread out over several days.
The size of the surface vessels varies in accordance with the test
requirements and vessel availability. Often multiple surface craft are
required to support a single test event.
Acting as a support platform for testing, surface vessels would be
utilized to carry test equipment and personnel to and from the test
sites and are also used to secure and monitor the designated test area.
Normally, these vessels remain on site and return to port following the
completion of the test; occasionally, however, they remain on station
throughout the duration of the test cycle for guarding sensitive
equipment in the water.
Additional vessels would be used for support activities that
include tows, and deployment and recovery of equipment. Tows involve
either transporting the system to the designated test area where it is
deployed and towed over a pre-positioned inert minefield or towing the
system from ashore for operation in the designated test area. Surface
vessels are also used to perform the deployment and recovery of the
RMMV, mine-like objects, and other test systems. Surface vessels that
are used in this manner normally return to port the same day. However,
this is test dependent, and under certain circumstance the surface
vessel may be required to remain on site for an extended period of
time.
Sonar Operations
For the proposed action, the Navy would test the Q-20 for up to 420
hours of active sonar use for 12 months starting in April 2012. Q-20
sonar operations involve the testing of various sonar systems at sea as
a means of demonstrating the systems' software capability to detect,
locate, and characterize mine-like objects under various environmental
conditions. The data collected is used to validate the sonar systems'
effectiveness and capability to meet its mission.
As sound travels through water, it creates a series of pressure
disturbances. Frequency is the number of complete cycles a sound or
pressure wave occurs per unit of time (measured in cycles per second,
or hertz (Hz)). The Navy has characterized low, mid, or high frequency
active sonars as follows:
Low-frequency active sonar (LFAS)--Below 1 kilohertz (kHz)
(low-frequency sound sources will not be used during any Q-20 test
operations)
Mid-frequency active sonar (LFAS)--From 1 to 10 kHz (mid-
frequency source sources will not be used during any Q-20 test
operations)
High-frequency active sonar (HFAS)--Above 10 kHz (only
high-frequency sound sources would be used during Q-20 test operations)
The Q-20 sonar systems proposed to be tested within the Q-20 Study
Area range in frequencies from 35 kHz to > 200 kHz, therefore, these
are HFAS systems. Those systems that operate at very high frequencies
(i.e., > 200 kHz), well above the hearing sensitivities of any marine
mammals, are not considered to affect marine mammals. Therefore, they
are not included in this document. The source levels associated with Q-
20 sonar systems that could affect marine mammals range from 207
decibels (dB) re 1 micro pascal ([mu]Pa) at 1 meter (m) to 212 dB re 1
[mu]Pa at 1 m. Operating parameters of the Q-20 sonar systems can be
found in Appendix A, Supplemental Information for Underwater Noise
Analysis of the Navy's IHA application.
The Q-20 Study Area includes Target and Operational Test Fields
located in W-151, an area within the Gulf of Mexico (GOM) subject to
military operations which also encompasses the Panama City Operating
Area (Figure 2-1 of the Navy's IHA application). The Q-20 test
activities will be conducted in the non-territorial waters off the
United States (beyond 12 nautical miles) in the GOM. The locations and
environments include:
Wide coastal shelf to 183 meters (m) [600 feet (ft)].
Water temperature range of 27 degrees Celsius ([deg]C) [80
degrees Fahrenheit ([deg]F)] in summer to 10 [deg]C (50 [deg]F) in
winter.
Mostly sandy bottom and good underwater visibility.
Seas less than 0.91 m (3 ft) 80 percent of the time in
summer and 50 percent of the time in winter.
The Navy requests an IHA for a time period of one year beginning
April, 2012. A total of 42 Q-20 test days will be conducted with a
maximum sonar operation of 10 hours in a single day.
Description of Marine Mammals in the Area of the Specified Activity
There are 29 marine mammal species under NMFS' jurisdiction that
may occur in the Q-20 Study Area (Table 1). These include 7 mysticetes
(baleen whales) and 22 odontocetes (toothed whales). Table 1 also
includes the Federal status of these marine mammal species. Six of
these marine mammal species under NMFS' jurisdiction are also listed as
federally endangered under the Endangered Species Act (ESA) and could
potentially occur in the Study Area: the humpback whale, North Atlantic
right whale, sei whale, fin whale, blue whale, and sperm whale. Of
these 29 species with occurrence records in the Q-20 Study Area, 22
species regularly occur there. These 22 species are: Bryde's whale,
sperm whale, pygmy sperm whale, dwarf sperm whale, Cuvier's beaked
whale, Gervais' beaked whale, Sowerby's beaked whale, Blainville's
beaked whale, killer whale, false killer whale, pygmy killer whale,
short-finned pilot whale, Risso's dolphin, melon-headed whale, rough-
toothed dolphin, bottlenose dolphin, Atlantic spotted dolphin,
pantropical spotted dolphin, striped dolphin, spinner dolphin, Clymene
dolphin, and Fraser's dolphin. The remaining 7 species (i.e., North
Atlantic right whale, humpback whale, sei whale, fin whale, blue whale,
minke whale, and True's beaked whale) are extralimital and are excluded
from further consideration of impacts from the NSWC PCD Q-20 testing
analysis.
Table 1--Marine Mammal Species Potentially Found in the Q-20 Study Area
------------------------------------------------------------------------
Family and scientific name Common name Federal status
------------------------------------------------------------------------
Order Cetacea
------------------------------------------------------------------------
Suborder Mysticeti (baleen whales)
------------------------------------------------------------------------
Eubalaena glacialis.......... North Atlantic Endangered
right whale.
Megaptera novaeangliae....... Humpback whale. Endangered.
Balaenoptera acutorostrata... Minke whale....
B. brydei.................... Bryde's whale..
B. borealis.................. Sei whale...... Endangered.
B. physalus.................. Fin whale...... Endangered.
[[Page 12013]]
B. musculus.................. Blue whale..... Endangered.
------------------------------------------------------------------------
Suborder Odontoceti (toothed whales)
------------------------------------------------------------------------
Physeter macrocephalus....... Sperm whale.... Endangered.
Kogia breviceps.............. Pygmy sperm
whale.
K. sima...................... Dwarf sperm
whale.
Ziphius cavirostris.......... Cuvier's beaked
whale.
Mesoplodon europaeus......... Gervais' beaked
whale.
M. Mirus..................... True's beaked
whale.
M. bidens.................... Sowerby's
beaked whale.
M. densirostris.............. Blainville's
beaked whale.
Steno bredanensis............ Rough-toothed
dolphin.
Tursiops truncatus........... Bottlenose
dolphin.
Stenella attenuata........... Pantropical
spotted
dolphin.
S. frontalis................. Atlantic
spotted
dolphin.
S. longirostris.............. Spinner dolphin
S. clymene................... Clymene dolphin
S. coeruleoalba.............. Striped dolphin
Lagenodephis hosei........... Fraser's
dolphin.
Grampus griseus.............. Risso's dolphin
Peponocephala electra........ Melon-headed
whale.
Feresa attenuata............. Pygmy killer
whale.
Pseudorca crassidens......... False killer
whale.
Orcinus orca................. Killer whale...
Globicephala macrorhynchus... Short-finned
pilot whale.
------------------------------------------------------------------------
The information contained herein relies heavily on the data
gathered in the Marine Resource Assessments (MRAs). The Navy Marine
Resources Assessment (MRA) program was implemented by the Commander,
United States Fleet Forces Command, to collect data and information on
the protected and commercial marine resources found in the Department
of the Navy's (DON's) operating areas. Specifically, the goal of the
MRA program is to describe and document the marine resources present in
each of the Navy's Operating Areas. As such, an MRA has been completed
for the GOM Testing and Training Areas, which comprise three adjacent
Operating Areas, one of which is the Panama City Operating Area (DON,
2007). The DON 2007 is the most current MRA for the GOM.
The MRA represents a compilation and synthesis of available
scientific literature (e.g., journals, periodicals, theses,
dissertations, project reports, and other technical reports published
by government agencies, private businesses, or consulting firms) and
NMFS reports, including stock assessment reports (SARs), recovery
plans, and survey reports. The MRAs summarize the physical environment
(e.g., marine geology, circulation and currents, hydrography, and
plankton and primary productivity) for each test area. In addition, an
in-depth discussion of the biological environment (marine mammals, sea
turtles, fish, and EFH), as well as fishing grounds (recreational and
commercial) and other areas of interest (e.g., maritime boundaries,
navigable waters, marine managed areas, recreational diving sites) are
also provided. Where applicable, the information contained in the MRA
was used for analyses in this document.
A detailed description of marine mammal density estimates and their
distribution in the Q-20 Study Area is provided in the Navy's Q-20 IHA
application.
A 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 document. A summary is included below.
Sound is a wave of pressure variations propagating through a medium
(for the sonar considered in this proposed rule, the medium is marine
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, it is derived 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 (Urick, 1983).
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 tenfold increase in power (e.g., 20 dB is a 100-fold
increase, 30 dB is a 1,000-fold increase). Humans perceive a 10-dB
increase in noise as a doubling of sound level, or a 10 dB decrease in
noise as a halving of sound level. The term ``sound pressure level''
implies a decibel measure and a reference pressure that is used as the
denominator of the ratio. Throughout this document, NMFS uses 1
[micro]Pa as a standard reference pressure unless noted otherwise.
It is important to note that decibels underwater and decibels in
air are not the same and cannot be directly compared. To estimate a
comparison between sound in air and underwater, because of the
different densities of air and water and the different decibel
standards (i.e., reference pressures) in water and air, a sound with
the same intensity (i.e., power) in air and in water would be
approximately 63 dB lower in air. Thus, a sound that is 160 dB loud
underwater would have the same approximate effective intensity as a
sound that is 97 dB loud in air.
Sound frequency is measured in cycles per second, or Hertz
(abbreviated Hz), and is analogous to musical pitch;
[[Page 12014]]
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
and ultrasonic 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;'' airguns are an example
of a broadband sound source and 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. Based
on available behavioral data, audiograms derived using auditory evoked
potential, anatomical modeling, and other data, Southall et al. (2007)
designate ``functional hearing groups'' and estimate the lower and
upper frequencies of functional hearing of the groups. Further, the
frequency range in which each group's hearing is estimated as being
most sensitive is represented in the flat part of the M-weighting
functions developed for each group. The functional groups and the
associated frequencies are indicated below:
Low-frequency cetaceans (13 species of mysticetes):
Functional hearing is estimated to occur between approximately 7 Hz and
22 kHz.
Mid-frequency cetaceans (32 species of dolphins, six
species of larger toothed whales, and 19 species of beaked and
bottlenose whales): Functional hearing is estimated to occur between
approximately 150 Hz and 160 kHz.
High-frequency cetaceans (eight species of true porpoises,
six species of river dolphins, Kogia, the franciscana, and four species
of cephalorhynchids): Functional hearing is estimated to occur between
approximately 200 Hz and 180 kHz.
Pinnipeds in Water: Functional hearing is estimated to
occur between approximately 75 Hz and 75 kHz, with the greatest
sensitivity between approximately 700 Hz and 20 kHz.
Pinnipeds in Air: Functional hearing is estimated to occur
between approximately 75 Hz and 30 kHz.
Because ears adapted to function underwater are physiologically
different from human ears, comparisons using decibel measurements in
air would still not be adequate to describe the effects of a sound on a
whale. When sound travels away from its source, its loudness decreases
as the distance traveled (propagates) by the sound increases. Thus, the
loudness of a sound at its source is higher than the loudness of that
same sound a kilometer distant. Acousticians often refer to the
loudness of a sound at its source (typically measured one meter from
the source) as the source level and the loudness of sound elsewhere as
the received level. For example, a humpback whale three kilometers from
an airgun that has a source level of 230 dB may only be exposed to
sound that is 160 dB loud, depending on how the sound propagates. As a
result, it is important not to confuse source levels and received
levels when discussing the loudness of sound in the ocean.
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 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 Document
This section includes a brief explanation of the two sound
measurements (sound pressure level (SPL) and sound exposure level
(SEL)) frequently used in the discussions of acoustic effects in this
document.
SPL
Sound pressure is the sound force per unit area, and is usually
measured in microPa, 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 ratio of a measured sound pressure and a reference
level. 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 (in dB) = 20 log (pressure/reference pressure)
SPL is an instantaneous measurement and can be expressed as the
peak, the peak-peak, or the root mean square (rms). Root mean square,
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
document refer to the root mean square. SPL does not take the duration
of a sound 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).
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 microPa\2\-s.
SEL = SPL + 10 log(duration in seconds)
As applied to tactical 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 total SEL. The total 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 in SEL.
Potential Impacts to Marine Mammal Species
The Navy considers that the proposed Q-20 sonar testing activities
in the Q-20 Study Area could potentially result in harassment to marine
mammals. Although surface operations related to sonar testing involve
ship movement in the vicinity of the Q-20 test area, NMFS considers it
unlikely that ship strike could occur as analyzed below.
Surface Operations
Typical operations occurring at the surface include the deployment
or towing of mine countermeasures (MCM) equipment, retrieval of
equipment, and clearing and monitoring for non-participating vessels.
As such, the potential exists for a ship to strike a
[[Page 12015]]
marine mammal while conducting surface operations. In an effort to
reduce the likelihood of a vessel strike, the mitigation and monitoring
measures discussed below would be implemented.
Collisions with commercial and U.S. Navy vessels can cause major
wounds and may occasionally cause fatalities to marine mammals. 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). Laist et al. (2001)
identified 11 species known to be hit by ships worldwide. Of these
species, fin whales are struck most frequently; followed by right
whales, humpback whales, sperm whales, and gray whales. More
specifically, from 1975 through 1996, there were 31 dead whale
strandings involving four large whales along the GOM coastline.
Stranded animals included two sei whales, four minke whales, eight
Bryde's whales, and 17 sperm whales. Only one of the stranded animals,
a sperm whale with propeller wounds found in Louisiana on 9 March 1990,
was identified as stranding as a result of a possible ship strike
(Laist et al., 2001). In addition, from 1999 through 2003, there was
only one stranding involving a false killer whale in the northern GOM
(Alabama 1999) (Waring et al., 2006). According to the 2010 Stock
Assessment Report (NMFS 2011), during 2009 there was one known Bryde's
whale mortality as a result of a ship strike. Otherwise, no other
marine mammal that is likely to occur in the northern GOM has been
reported as either seriously or fatally injured as a result of a ship
strike from 1999 through 2009 (Waring et al., 2007).
It is unlikely that activities in non-territorial waters will
result in a ship strike because of the nature of the operations and
size of the vessels. For example, the hours of surface operations take
into consideration operation times for multiple vessels during each
test event. These vessels range in size from small Rigid Hull
Inflatable Boat (RHIB) to surface vessels of approximately 420 feet.
The majority of these vessels are small RHIBs and medium-sized vessels.
A large proportion of the timeframe for the Q-20 test events include
periods when ships remain stationary within the test site.
The greatest time spent in transit for tests includes navigation to
and from the sites. At these times, the Navy follows standard operating
procedures (SOPs). The captain and other crew members keep watch during
ship transits to avoid objects in the water. Furthermore, with the
implementation of the proposed mitigation and monitoring measures
described below, NMFS believes that it is unlikely vessel strikes would
occur. Consequently, because of the nature of the surface operations
and the size of the vessels, the proposed mitigation and monitoring
measures, and the fact that cetaceans typically more vulnerable to ship
strikes are not likely to be in the project area, the NMFS concludes
that ship strikes are unlikely to occur in the Q-20 Study Area.
Acoustic Effects: Exposure to Sonar
For activities involving active tactical sonar, NMFS's analysis
will identify the probability of lethal responses, physical trauma,
sensory impairment (permanent and temporary threshold shifts and
acoustic masking), physiological responses (particular stress
responses), behavioral disturbance (that rises to the level of
harassment), and social responses that would be classified as
behavioral harassment or injury and/or would be likely to adversely
affect the species or stock through effects on annual rates of
recruitment or survival. In this section, we will focus qualitatively
on the different ways that exposure to sonar signals may affect marine
mammals. Then, in the Estimated Take of Marine Mammals section, NMFS
will relate the potential effects on marine mammals from sonar exposure
to the MMPA regulatory definitions of Level A and Level B Harassment
and attempt to quantify those effects.
Direct Physiological Effects
Based on the literature, there are two basic ways that Navy sonar
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 recognize them) following exposure to a
sufficiently intense sound, 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 recovery), occurs in specific
frequency ranges (e.g., 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 by only 6 dB or reduced by 30 dB). PTS is permanent
(i.e., there is no recovery), but also occurs in a specific frequency
range and amount as mentioned in the TTS description.
The following physiological mechanisms are thought to play a role
in inducing auditory TSs: Effects on 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 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. For continuous sounds, exposures of
equal energy (the same SEL) will lead to approximately equal effects.
For intermittent sounds, less TS will occur than from a continuous
exposure with the same energy (some recovery will occur between
exposures) (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, very
prolonged exposure to sound 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 Navy sonar, 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, 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
[[Page 12016]]
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 cetaceans, published data are limited to the captive
bottlenose dolphin and beluga whale (Finneran et al., 2000, 2002b,
2005a; Schlundt et al., 2000; Nachtigall et al., 2003, 2004).
Marine mammal hearing plays a critical role in communication with
conspecifics, and interpreting environmental cues for purposes such as
predator avoidance and prey capture. Depending on the frequency range
of TTS degree (dB), duration, 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 takes place during a time
when the animal is traveling through the open ocean, 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 a 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 long term condition. Of note, reduced hearing sensitivity as a
simple function of development and aging has been observed in marine
mammals, as well as humans and other taxa (Southall et al., 2007), so
we can infer that strategies exist for coping with this condition to
some degree, though likely not without cost. There is no empirical
evidence that exposure to Navy sonar can cause PTS in any marine
mammals; instead the probability of PTS has been inferred from studies
of TTS (see Richardson et al., 1995).
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., 2001). 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. Recent work conducted by Crum et al. (2005)
demonstrated the possibility of rectified diffusion for short duration
signals, but at sound exposure levels and tissue saturation levels that
are improbable to occur in a diving marine mammal. 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. 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). In this scenario, the rate of ascent would
need to be sufficiently rapid to compromise behavioral or physiological
protections against nitrogen bubble formation. 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, 2002).
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 (Hooker et al., 2011). However, Jepson et al. (2003, 2005) and
Fernandez et al. (2004, 2005) 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. A recent review of evidence for gas-bubble incidence in
marine mammal tissues suggest that diving mammals vary their
physiological responses according to multiple stressors, and that the
perspective on marine mammal diving physiology should change from
simply minimizing nitrogen loading to management of the nitrogen load
(Hooker et al., 2011). This suggests several avenues for further study,
ranging from the effects of gas bubbles at molecular, cellular and
organ function levels, to comparative studies relating the presence/
absence of gas bubbles to diving behavior. More information regarding
hypotheses that attempt to explain how behavioral responses to Navy
sonar can lead to strandings is included in the Behaviorally Mediated
Bubble Growth section, after the summary of strandings.
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; Clark et al.,
2009). 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
[[Page 12017]]
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 also decreases. This principle is also expected to apply to
marine mammals because of common biomechanical cochlear properties
across taxa.
Richardson et al. (1995) 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 odontocetes (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).
As mentioned previously, the functional hearing ranges of
mysticetes (baleen whales) and odontocetes (toothed whales) all
encompass the frequencies of the sonar sources used in the Navy's Q-20
test activities. Additionally, almost all species' vocal repertoires
span across the frequencies of the 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. However, because the
pulse length and duty cycle of the Navy sonar signals are of short
duration and would not be continuous, masking is unlikely to occur as a
result of exposure to these signals during the Q-20 test activities in
the designated Q-20 Study Area.
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 are more important than
detecting a vocalization (Brenowitz, 1982; Brumm et al., 2004; Dooling,
2004; Marten and Marler, 1977; Patricelli et al., 2006). Most animals
that vocalize have evolved an ability to make vocal adjustments to
their vocalizations to increase the signal-to-noise ratio, active
space, and recognizability of their vocalizations in the face of
temporary changes in background noise (Brumm et al., 2004; Patricelli
et al., 2006). Vocalizing animals will make one or more of the
following adjustments to their vocalizations: Adjust the frequency
structure; adjust the amplitude; adjust temporal structure; or adjust
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
response.
In the case of many stressors, an animal's first and 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
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 associate with ``stress.'' These
responses have a relatively short duration and may or may not have
significant long-term effects on an animal's welfare.
An animal's third line of defense to stressors involves its
neuroendocrine or sympathetic nervous 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) and 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; 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
[[Page 12018]]
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
functions, which impair 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'' (sensu Seyle, 1950) or ``allostatic
loading'' (sensu McEwen and Wingfield, 2003). This pathological state
will last until the animal replenishes its biotic reserves sufficient
to restore normal function.
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). Although no information has been collected on the physiological
responses of marine mammals to exposure to anthropogenic sounds,
studies of other marine animals and terrestrial animals would 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 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 physiology stress responses of
endangered Sonoran pronghorn to military overflights. Smith et al.
(2004a, 2004b) identified noise induced physiological transient stress
responses in hearing-specialist fish 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 cetaceans 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
cetaceans 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 be as significant as behavioral
responses to TTS.
Behavioral Disturbance
Behavioral responses to sound are highly variable and context-
specific. Exposure of marine mammals to sound sources can result in
(but is not limited to) the following observable responses: 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).
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 type affects whether it is less likely
(habituation) or more likely (sensitization) to respond to certain
sounds in the future (animals can also be innately predisposed 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.
There are only a few empirical studies of behavioral responses of
free-living cetaceans to military sonar being conducted to date, due to
the difficulties in implementing experimental protocols on wild marine
mammals.
An opportunistic observation was made on a tagged Blainville's
beaked whale (Mesoplodon densirostris) before, during, and after a
multi-day naval exercises involving tactical mid-frequency sonars
within the U.S. Navy's sonar testing range at the Atlantic Undersea
Test and Evaluation Center (AUTEC), in the Tongue of the Ocean near
Andros Island in the Bahamas (Tyack et al., 2011). The adult male whale
was tagged with a satellite transmitter tag on May 7, 2009. During the
72 hrs before the sonar exercise started, the mean distance from whale
to the center of the AUTEC range was approximately 37 km. During the 72
hrs sonar exercise, the whale moved several tens of km farther away
(mean distance approximately 54 km). The received sound levels at the
tagged whale during sonar exposure were estimated to be 146 dB re 1
[micro]Pa at the highest level. The tagged whale slowly returned for
several days after the exercise stopped (mean distance approximately 29
km) from 0-72 hours after the exercise stopped (Tyack et al., 2011).
In the past several years, controlled exposure experiments (CEE) on
marine mammal behavioral responses to military sonar signals using
acoustic tags have been started in the Bahamas, the Mediterranean Sea,
southern California, and Norway. These behavioral response studies
(BRS), though still in their early stages, have provided some
preliminary insights into
[[Page 12019]]
cetacean behavioral disturbances when exposed to simulated and actual
military sonar signals.
In 2007 and 2008, two Blainville's beaked whales were tagged in the
AUTEC range and exposed to simulated mid-frequency sonar signals,
killer whale (Orcinus orca) recordings (in 2007), and pseudo-random
noise (PRN, in 2008) (Tyack et al., 2011). For the simulated mid-
frequency exposure BRS, the tagged whale stopped clicking during its
foraging dive after 9 minutes when the received level reached 138 dB
SPL, or a cumulative SEL value of 142 dB re 1 [micro]Pa\2\-s. Once the
whale stopped clicking, it ascended slowly, moving away from the sound
source. The whale surfaced and remained in the area for approximately 2
hours before making another foraging dive (Tyack et al., 2011).
The same beaked whale was exposed to killer whale sound recording
during its subsequent deep foraging dive. The whale stopped clicking
about 1 minute after the received level of the killer whale sound
reached 98 dB SPL, just above the ambient noise level at the whale. The
whale then made a long and slow ascent. After surfacing, the whale
continued to swim away from the playback location for 10 hours (Tyack
et al., 2011).
In 2008, a Blainville's beaked was tagged and exposed with PRN that
has the same frequency band as the simulated mid-frequency sonar
signal. The received level at the whale ranged from inaudible to 142 dB
SPL (144 dB cumulative SEL). The whale stopped clicking less than 2
minutes after exposure to the last transmission and ascended slowly to
approximately 600 m. The whale appeared to stop at this depth, at which
time the tag unexpectedly released from the whale (Tyack et al., 2011).
During CEEs of the BRS off Norway, social behavioral responses of
pilot whales and killer whales to tagging and sonar exposure were
investigated. Sonar exposure was sampled for 3 pilot whale
(Globicephala spp.) groups and 1 group of killer whales. Results show
that when exposed to sonar signals, pilot whales showed a preference
for larger groups with medium-low surfacing synchrony, while starting
logging, spyhopping and milling. While killer whales showed the
opposite pattern, maintaining asynchronous patterns of surface
behavior: decreased surfacing synchrony, increased spacing, decreased
group size, tailslaps and loggings (Visser et al., 2011).
Although the small sample size of these CEEs reported here is too
small to make firm conclusions about differential responses of
cetaceans to military sonar exposure, none of the results showed that
whales responded to sonar signals with panicked flight. Instead, the
beaked whales exposed to simulated sonar signals and killer whale sound
recording moved in a well oriented direction away from the source
towards the deep water exit from the Tongue of the Ocean (Tyack et al.,
2011). In addition, different species of cetaceans exhibited different
social behavioral responses towards (close) vessel presence and sonar
signals, which elicit different, potentially tailored and species-
specific responses (Visser et al., 2011).
Much more qualitative information is available on the avoidance
responses of free-living cetaceans to other acoustic sources, like
seismic airguns and low-frequency active sonar, than mid-frequency
active sonar. Richardson et al., (1995) noted that avoidance reactions
are the most obvious manifestations of disturbance in marine mammals.
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 man-made sound with the goal of proposing exposure
criteria for certain effects. This compilation of literature is very
valuable, though Southall et al. note that not all data is 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.
In the Southall et al., (2007) report, 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. HFAS/MFAS sonar is
considered a non-pulse sound. Southall et al., (2007) summarize the
reports associated with low-, mid-, and high-frequency cetacean
responses to non-pulse sounds (there are no pinnipeds in the Gulf of
Mexico (GOM)) in Appendix C of their report (incorporated by reference
and summarized in the three paragraphs below).
The reports 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 HFAS/MFAS)
including: Vessel noise, drilling and machinery playback, low frequency
M-sequences (sine wave with multiple phase reversals) playback, low
frequency active sonar playback, drill vessels, Acoustic Thermometry of
Ocean Climate (ATOC) source, and non-pulse playbacks. These reports
generally indicate no (or very limited) responses to received levels in
the 90 to 120 dB re 1 [micro]Pa range and an increasing likelihood of
avoidance and other behavioral effects in the 120 to 160 dB range. As
mentioned earlier, however, 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 reports 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 HFAS/MFAS) including: Pingers, drilling playbacks, vessel
and ice-breaking noise, vessel noise, Acoustic Harassment Devices
(AHDs), Acoustic Deterrent Devices (ADDs), HFAS/MFAS, and non-pulse
bands and tones. Southall et al. were unable to come to a clear
conclusion regarding these reports. 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 responded at lower levels in the field).
The reports that address the 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 HFAS/MFAS) including: Acoustic harassment devices,
Acoustical Telemetry of Ocean Climate (ATOC), wind turbine, vessel
noise, and construction noise. However, no conclusive results are
available from these reports. In some cases, high frequency cetaceans
(harbor porpoises) are observed to be quite sensitive to a wide range
of human sounds at very low exposure RLs (90 to 120 dB). All recorded
exposures exceeding 140 dB produced profound and sustained
[[Page 12020]]
avoidance behavior in wild harbor porpoises (Southall et al., 2007).
In addition to summarizing the available data, the authors of
Southall et al. (2007) developed a severity scaling system with the
intent of ultimately being able to assign some level of biological
significance to a response. Following is a summary of their scoring
system, a comprehensive list of the behaviors associated with each
score may be found in the report:
0-3 (Minor and/or brief behaviors) includes, but is not
limited to: No response; minor changes in speed or locomotion (but with
no avoidance); individual alert behavior; minor cessation in vocal
behavior; minor changes in response to trained behaviors (in
laboratory).
4-6 (Behaviors with higher potential to affect foraging,
reproduction, or survival) includes, but is not limited to: Moderate
changes in speed, direction, or dive profile; brief shift in group
distribution; prolonged cessation or modification of vocal behavior
(duration > duration of sound); minor or moderate individual and/or
group avoidance of sound; brief cessation of reproductive behavior; or
refusal to initiate trained tasks (in laboratory).
7-9 (Behaviors considered likely to affect the
aforementioned vital rates) includes, but are not limited to: Extensive
of prolonged aggressive behavior; moderate, prolonged or significant
separation of females and dependent offspring with disruption of
acoustic reunion mechanisms; long-term avoidance of an area; outright
panic, stampede, stranding; threatening or attacking sound source (in
laboratory).
In Table 2 we have summarized the scores that Southall et al.
(2007) assigned to the papers that reported behavioral responses of
low-frequency cetaceans, mid-frequency cetaceans, and high-frequency
cetaceans to non-pulse sounds.
Table 4--Data Compiled From Three Tables From Southall et al. (2007) Indicating When Marine Mammals (Low-Frequency Cetacean = L, Mid-Frequency Cetacean
= M, and High-Frequency Cetacean = H) Were Reported as Having a Behavioral Response of the Indicated Severity to a Non-Pulse Sound of the Indicated
Received Level. As Discussed in the Text, Responses Are Highly Variable and Context Specific
--------------------------------------------------------------------------------------------------------------------------------------------------------
Received RMS sound pressure level (dB re 1 microPa)
---------------------------------------------------------------------------------------------------------------------------------------------------------
90 to 100 to 110 to 120 to 130 to 140 to 150 to 160 to 170 to 180 to 190 to
Response score 80 to <90 <100 <110 <120 <130 <140 <150 <160 <170 <180 <190 <200
--------------------------------------------------------------------------------------------------------------------------------------------------------
9................... ......... ......... ......... ......... ......... ......... ......... ......... ......... ......... ......... .........
8................... ......... M M ......... M ......... M ......... ......... ......... M M
7................... ......... ......... ......... ......... ......... L L ......... ......... ......... ......... .........
6................... H L/H L/H L/M/H L/M/H L L/H H M/H M ......... .........
5................... ......... ......... ......... ......... M ......... ......... ......... ......... ......... ......... .........
4................... ......... ......... H L/M/H L/M ......... L ......... ......... ......... ......... .........
3................... ......... M L/M L/M M ......... ......... ......... ......... ......... ......... .........
2................... ......... ......... L L/M L L L ......... ......... ......... ......... .........
1................... ......... ......... M M M ......... ......... ......... ......... ......... ......... .........
0................... L/H L/H L/M/H L/M/H L/M/H L M ......... ......... ......... M M
--------------------------------------------------------------------------------------------------------------------------------------------------------
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 little 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
unconsciously (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 (Anser
[[Page 12021]]
brachyrhynchus) in undisturbed habitat gained body mass and had about a
46-percent reproductive success 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. Similar reductions in reproductive success have been reported
for mule deer (Odocoileus hemionus) 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 jetfights (Luick et al., 1996), and caribou disturbed by low-
elevation jet flights (Harrington and Veitch, 1992). Similarly, a study
of elk (Cervus elaphus) 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 (Ursus
horribilis) reported that bears disturbed by hikers reduced their
energy intake by an average of 12 kcal/min (50.2 x 103kJ/min), and
spent energy fleeing or acting aggressively toward hikers (White et
al., 1999).
On a related note, many animals perform vital functions, such as
feeding, resting, traveling, and socializing, on a diel cycle (24-hr
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 one day
and not recurring on subsequent days is not considered particularly
severe unless it could directly affect reproduction or survival
(Southall et al., 2007).
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). 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 stranding are unknown (Geraci et al., 1976; Eaton,
1979, Odell et al., 1980; Best, 1982).
Several sources have published lists of mass stranding events of
cetaceans during attempts 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
(IWC, 2005) identified 10 mass stranding events of Cuvier's beaked
whales that had been reported and one mass stranding of four Baird's
beaked whales (Berardius bairdii). The IWC concluded that, out of eight
stranding events reported from the mid-1980s to the summer of 2003,
seven had been associated with the use of mid-frequency sonar, one of
those seven had been associated with the use of low frequency sonar,
and the remaining stranding event had been associated with the use of
seismic airguns. None of the strandings has been associated with high
frequency sonar such as the Q-20 sonar proposed to be tested in this
action. Therefore, NMFS does not consider it likely that the proposed
Q-20 testing activity would cause marine mammals to strand.
Effects on Marine Mammal Habitat
There are no areas within the NSWC PCD that are specifically
considered as important physical habitat for marine mammals.
The prey of marine mammals are considered part of their habitat.
The Navy's Final Environmental Impact Statement and Overseas
Environmental Impact Statement (FEIS) on the research, development,
test and evaluation activities in the NSWC PCD study area contains a
detailed discussion of the potential effects to fish from HFAS/MFAS.
These effects are the same as expected from the proposed Q-20 sonar
testing activities within the same area.
The extent of data, and particularly scientifically peer-reviewed
data, on the effects of high intensity sounds on fish is limited. In
considering the available literature, the vast majority of fish species
studied to date are hearing generalists and cannot hear sounds above
500 to 1,500 Hz (depending upon the species), and, therefore,
behavioral effects on these species from higher frequency sounds are
not likely. Moreover, even those fish species that may hear above 1.5
kHz, such as a few sciaenids and the clupeids (and relatives), have
relatively poor hearing above 1.5 kHz as compared to their hearing
sensitivity at lower frequencies. Therefore, even among the species
that have hearing ranges that overlap with some mid- and high-frequency
sounds, it is likely that the fish will only actually hear the sounds
if the fish and source are very close to one another. Finally, since
the vast majority of sounds that are of biological relevance to fish
are below 1 kHz (e.g., Zelick et al., 1999; Ladich and Popper, 2004),
even if a fish detects a mid-or high-frequency sound, these sounds will
not mask detection of lower frequency biologically relevant sounds.
Based on the above information, there will likely be few, if any,
behavioral impacts on fish.
Alternatively, it is possible that very intense mid- and high-
frequency signals could have a physical impact on fish, resulting in
damage to the swim bladder and other organ systems. However, even these
kinds of effects have only been shown in a few cases in response to
explosives, and only when the fish has been very close to the source.
Such effects have never been indicated in response to any Navy sonar.
Moreover, at greater distances (the distance clearly would depend on
the intensity of the signal from the source) there appears to be little
or no impact on fish, and particularly no impact on fish that do not
have a swim bladder or other air bubble that would be affected by rapid
pressure changes.
Proposed Mitigation Measures
In order to issue an incidental take authorization (ITA) under
Section 101(a)(5)(D) 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.'' The National Defense
Authorization Act (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 Q-20 sonar testing
activities described in the Navy's IHA application are considered
military readiness activities.
For the proposed Q-20 sonar testing activities in the GOM, NMFS
worked with the Navy to develop mitigation
[[Page 12022]]
measures. The Navy then proposed the following mitigation measures,
which include a careful balancing of minimizing impacts to marine
mammals with the likely effect of that measure on personnel safety,
practicality of implementation, and impact on the ``military-readiness
activity''.
Personnel Training
Marine mammal mitigation training for those who participate in the
active sonar activities is a key element of the protective measures.
The goal of this training is for key personnel onboard Navy platforms
in the Q-20 Study Area to understand the protective measures and be
competent to carry them out. The Marine Species Awareness Training
(MSAT) is provided to all applicable participants, where appropriate.
The program addresses environmental protection, laws governing the
protection of marine species, Navy stewardship, and general observation
information including more detailed information for spotting marine
mammals. Marine mammal observer training will be provided before active
sonar testing begins.
Marine observers would be aware of the specific actions to be taken
based on the RDT&E platform if a marine mammal is observed.
Specifically, the following requirements for personnel training would
apply:
All marine observers onboard platforms involved in the Q-
20 sonar test activities will review the NMFS-approved MSAT material
prior to use of active sonar.
Marine Observers shall be trained in marine mammal
recognition. Marine Observer training shall include completion of the
Marine Species Awareness Training, instruction on governing laws and
policies, and overview of the specific Gulf of Mexico species present,
and observer roles and responsibilities.
Marine observers will be trained in the most effective
means to ensure quick and effective communication within the command
structure in order to facilitate implementation of mitigation measures
if marine species are spotted.
Range Operating Procedures
The following procedures would be implemented to maximize the
ability of Navy personnel to recognize instances when marine mammals
are in the vicinity.
(1) Observer Responsibilities
Marine observers will have at least one set of binoculars
available for each person to aid in the detection of marine mammals.
Marine observers will scan the water from the ship to the
horizon and be responsible for all observations in their sector. In
searching the assigned sector, the lookout will always start at the
forward part of the sector and search aft (toward the back). To search
and scan, the lookout will hold the binoculars steady so the horizon is
in the top third of the field of vision and direct the eyes just below
the horizon. The lookout will scan for approximately five seconds in as
many small steps as possible across the field seen through the
binoculars. They will search the entire sector in approximately five-
degree steps, pausing between steps for approximately five seconds to
scan the field of view. At the end of the sector search, the glasses
will be lowered to allow the eyes to rest for a few seconds, and then
the lookout will search back across the sector with the naked eye.
Observers will be responsible for informing the Test
Director of any marine mammal that may need to be avoided, as
warranted.
These procedures would apply as much as possible during
RMMV operations. When an RMMV is operating over the horizon, it is
impossible to follow and observe it during the entire path. An observer
will be located on the support vessel or platform to observe the area
when the system is undergoing a small track close to the support
platform.
(2) Operating Procedures
Test Directors will, as appropriate to the event, make use
of marine species detection cues and information to limit interaction
with marine species to the maximum extent possible, consistent with the
safety of the ship.
During Q-20 sonar activities, personnel will utilize all
available sensor and optical system (such as Night Vision Goggles) to
aid in the detection of marine mammals.
Navy aircraft participating will conduct and maintain,
when operationally feasible, required, 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.
Marine mammal detections by aircraft will be immediately
reported to the Test Director. This action will occur when it is
reasonable to conclude that the course of the ship will likely close
the distance between the ship and the detected marine mammal.
Exclusion Zones--The Navy will ensure that sonar
transmissions are ceased if any detected marine mammals are within 200
yards (183 m) of the sonar source. Active sonar will not resume until
the marine mammal has been seen to leave the area, has not been
detected for 30 minutes, or the vessel has transited more than 2,000
yards (1,828 m) beyond the location of the last detection.
Special conditions applicable for dolphins only: If, after
conducting an initial maneuver to avoid close quarters with dolphins,
the Test Director or the Test Director's designee concludes that
dolphins are deliberately closing to ride the vessel's bow wave, no
further mitigation actions are necessary while the dolphins or
porpoises continue to exhibit bow wave riding behavior.
Sonar levels (generally)--Navy will operate sonar at the
lowest practicable level, except as required to meet testing
objectives.
Clearance Procedures
When the test platform (surface vessel or aircraft) arrives at the
test site, an initial evaluation of environmental suitability will be
made. This evaluation will include an assessment of sea state and
verification that the area is clear of visually detectable marine
mammals and indicators of their presence. For example, large flocks of
birds and large schools of fish are considered indicators of potential
marine mammal presence.
If the initial evaluation indicates that the area is clear, visual
surveying will begin. The area will be visually surveyed for the
presence of protected species and protected species indicators. Visual
surveys will be conducted from the test platform before test activities
begin. When the platform is a surface vessel, no additional aerial
surveys will be required. For surveys requiring only surface vessels,
aerial surveys may be opportunistically conducted by aircraft
participating in the test.
Shipboard monitoring will be staged from the highest point possible
on the vessel. The observer(s) will be experienced in shipboard
surveys, familiar with the marine life of the area, and equipped with
binoculars of sufficient magnification. Each observer will be provided
with a two-way radio that will be dedicated to the survey, and will
have direct radio contact with the Test Director. Observers will report
to the Test Director any sightings of marine mammals or indicators of
these species, as described previously. Distance and bearing will be
provided when available. Observers may recommend a ``Go''/``No Go''
decision, but the final decision will be the responsibility of the Test
Director.
Post-mission surveys will be conducted from the surface vessel(s)
[[Page 12023]]
and aircraft used for pre-test surveys. Any affected marine species
will be documented and reported to NMFS. The report will include the
date, time, location, test activities, species (to the lowest taxonomic
level possible), behavior, and number of animals.
NMFS has carefully evaluated the Navy's proposed mitigation
measures and considered a 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 measure is expected to minimize
adverse impacts to marine mammals
The proven or likely efficacy of the specific measure to
minimize adverse impacts as planned; and
The practicability of the measure 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, we have preliminarily determined
that the proposed mitigation measures provide the 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.
Proposed Monitoring Measures
In order to issue an ITA for an activity, section 101(a)(5)(D) of
the MMPA states that 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.
The RDT&E Monitoring Program, proposed by the Navy as part of its
IHA application, is focused on mitigation-based monitoring. Main
monitoring techniques include use of civilian personnel as marine
mammal observers during pre-, during, and post-, test events.
Systematic monitoring of the affected area for marine mammals will
be conducted prior to, during, and after test events using aerial and/
or ship-based visual surveys. Observers will record information during
the test activity. Data recorded will include exercise information
(time, date, and location) and marine mammal and/or indicator presence,
species, number of animals, their behavior, and whether there are
changes in the behavior. Personnel will immediately report observed
stranded or injured marine mammals to NMFS stranding response network
and NMFS Regional Office. Reporting requirements will be included in
the Naval Surface Warfare Center Panama City Division (NSWC PCD)
Mission Activities Final Environmental Impact Statement/Overseas
Environmental Impact Statement Annual Activity report as required by
its Final Rule (DON, 2009; NMFS, 2010d).
Ongoing Monitoring
The Navy has an existing Monitoring Plan that provides for site-
specific monitoring for MMPA and Endangered Species Act (ESA) listed
species, primarily marine mammals within the Gulf of Mexico, including
marine water areas of the Q-20 Study Area (DON, 2009; NMFS, 2010d).
This monitoring plan was initially developed in support of the NSWC PCD
Mission Activities Final Environmental Impact Statement/Overseas
Environmental Impact Statement and subsequent Final Rule by NMFS (DON,
2009; NMFS, 2010d). The primary goals of monitoring are to evaluate
trends in marine species distribution and abundance in order to assess
potential population effects from Navy training and testing events and
determine the effectiveness of the Navy's mitigation measures. The
monitoring plan, adjusted annually in consultation with NMFS, includes
aerial- and ship-based visual observations, acoustic monitoring, and
other efforts such as oceanographic observations.
Estimated Take by Incidental Harassment
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].
Level B Harassment
Of the potential effects that were described in the Potential
Effects of Exposure of Marine Mammals to Sonar section, 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 active sonar exposure, is considered Level B Harassment. Some of the
lower level physiological stress responses will 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.
In the effects section above, we described the Southall et al.,
(2007) severity scaling system and listed some examples of the three
broad categories of behaviors: (0-3: Minor and/or brief behaviors); 4-6
(Behaviors with higher potential to affect foraging, reproduction, or
survival); 7-9 (Behaviors considered likely to affect the
aforementioned vital rates). Generally speaking, MMPA Level B
Harassment, as defined in this document, would include the behaviors
described in the 7-9 category, and a subset, dependent on context and
other considerations, of the behaviors described in the 4-6 categories.
Behavioral harassment generally does not include behaviors ranked 0-3
in Southall et al., (2007).
Acoustic Masking and Communication Impairment--Acoustic masking is
considered Level B Harassment as it can disrupt natural behavioral
patterns by interrupting or limiting the marine mammal's receipt or
transmittal of important information or environmental cues.
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
[[Page 12024]]
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 Navy sonar) as
Level B Harassment, not Level A Harassment (injury).
Level A Harassment
Of the potential effects that were described in the Potential
Effects of Exposure of Marine Mammal to Sonar section, following are
the types of effects that fall into the Level A Harassment category:
PTS--PTS (resulting from exposure to active sonar) 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 results in changes in the chemical
composition of the inner ear fluids.
Acoustic Take Criteria
For the purposes of an MMPA incidental take 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 military sonar cannot be detected or
measured, 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 uses acoustic criteria that estimate at what received
level (when exposed to Navy sonar) Level B Harassment and Level A
Harassment of marine mammals would occur. These acoustic criteria are
discussed below.
Relatively few applicable data exist to support acoustic criteria
specifically for HFAS (such as the Q-20 active sonar). However, because
MFAS systems have larger impact ranges, NMFS will apply the criteria
developed for the MFAS systems to the HFAS systems.
NMFS utilizes three acoustic criteria for HFAS/MFAS: PTS (injury--
Level A Harassment), behavioral harassment from TTS, and sub-TTS (Level
B Harassment). Because the TTS and PTS criteria are derived similarly
and the PTS criteria was extrapolated from the TTS data, the TTS and
PTS acoustic criteria will be presented first, before the behavioral
criteria.
For more information regarding these criteria, please see the
Navy's FEIS for the NSWC PCD (Navy 2009).
Level B Harassment Threshold (TTS)
As mentioned above, 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 is likely to occur are 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. NMFS also uses an
acoustic criteria to estimate the number of marine mammals that might
sustain TTS incidental to a specific activity (in addition to the
behavioral criteria).
A number of investigators have measured TTS in marine mammals.
These studies measured hearing thresholds in trained marine mammals
before and after exposure to intense sounds. The existing cetacean TTS
data are summarized in the following bullets.
Schlundt et al. (2000) reported the results of TTS
experiments conducted with 5 bottlenose dolphins and 2 belugas exposed
to 1-second tones. This paper also includes a reanalysis of preliminary
TTS data released in a technical report by Ridgway et al. (1997). At
frequencies of 3, 10, and 20 kHz, sound pressure levels (SPLs)
necessary to induce measurable amounts (6 dB or more) of TTS were
between 192 and 201 dB re 1 [mu]Pa (EL = 192 to 201 dB re 1 [mu]Pa\2\-
s). The mean exposure SPL and EL for onset-TTS were 195 dB re 1 [mu]Pa
and 195 dB re 1 [mu]Pa\2\-s, respectively.
Finneran et al. (2001, 2003, 2005) described TTS
experiments conducted with bottlenose dolphins exposed to 3-kHz tones
with durations of 1, 2, 4, and 8 seconds. Small amounts of TTS (3 to 6
dB) were observed in one dolphin after exposure to ELs between 190 and
204 dB re 1 microPa\2\-s. These results were consistent with the data
of Schlundt et al. (2000) and showed that the Schlundt et al. (2000)
data were not significantly affected by the masking sound used. These
results also confirmed that, for tones with different durations, the
amount of TTS is best correlated with the exposure EL rather than the
exposure SPL.
Nachtigall et al. (2003) measured TTS in a bottlenose
dolphin exposed to octave-band sound centered at 7.5 kHz. Nachtigall et
al. (2003a) reported TTSs of about 11 dB measured 10 to 15 minutes
after exposure to 30 to 50 minutes of sound with SPL 179 dB re 1 [mu]Pa
(EL about 213 dB re [mu]Pa\2\-s). No TTS was observed after exposure to
the same sound at 165 and 171 dB re 1 [mu]Pa. Nachtigall et al. (2004)
reported TTSs of around 4 to 8 dB 5 minutes after exposure to 30 to 50
minutes of sound with SPL 160 dB re 1 [mu]Pa (EL about 193 to 195 dB re
1 [mu]Pa \2\-s). The difference in results was attributed to faster
post exposure threshold measurement--TTS may have recovered before
being detected by Nachtigall et al. (2003). These studies showed that,
for long duration exposures, lower sound pressures are required to
induce TTS than are required for short-duration tones.
Finneran et al. (2000, 2002) conducted TTS experiments
with dolphins and belugas exposed to impulsive sounds similar to those
produced by distant underwater explosions and seismic waterguns. These
studies showed that, for very short-duration impulsive sounds, higher
sound pressures were required to induce TTS than for longer-duration
tones.
Some of the more important data obtained from these studies are
onset-TTS levels (exposure levels sufficient to cause a just-measurable
amount of TTS) often defined as 6 dB of TTS (for example, Schlundt et
al., 2000) and the fact that energy metrics (sound exposure levels
(SEL), which include a duration component) better predict when an
animal will sustain TTS than pressure (SPL) alone. NMFS' TTS criteria
(which indicate the received level at which onset TTS (>6dB) is
induced) for HFAS/MFAS are as follows:
Cetaceans--195 dB re 1 [mu]Pa \2\-s (based on mid-
frequency cetaceans--no published data exist on auditory effects of
noise in low or high frequency cetaceans) (Southall et al., 2007).
A detailed description of how TTS criteria were derived from the
results of the above studies may be found in
[[Page 12025]]
Chapter 3 of Southall et al. (2007), as well as the Navy's Q-20 IHA
application.
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 the 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 discovered through
study of terrestrial mammals. NMFS uses the following acoustic criteria
for injury:
Cetaceans--215 dB re 1 [micro]Pa\2\-s (based on mid-
frequency cetaceans--no published data exist on auditory effects of
noise in low or high frequency cetaceans) (Southall et al., 2007).
These criteria are based on a 20 dB increase in SEL over that
required for onset-TTS. Extrapolations from terrestrial mammal data
indicate that PTS occurs at 40 dB or more of TS, and that TS growth
occurs at a rate of approximately 1.6 dB TS per dB increase in EL.
There is a 34-dB TS difference between onset-TTS (6 dB) and onset-PTS
(40 dB). Therefore, an animal would require approximately 20-dB of
additional exposure (34 dB divided by 1.6 dB) above onset-TTS to reach
PTS. A detailed description of how TTS criteria were derived from the
results of the above studies may be found in Chapter 3 of Southall et
al. (2007), as well as the Navy's NSWC PCD LOA application. Southall et
al. (2007) recommend a precautionary dual criteria for TTS (230 dB re 1
[micro]Pa (SPL) in addition to 215 re 1 [micro]Pa\2\-s (SEL)) to
account for the potentially damaging transients embedded within non-
pulse exposures. However, in the case of HFAS/MFAS, the distance at
which an animal would receive 215 (SEL) is farther from the source than
the distance at which they would receive 230 (SPL) and therefore, it is
not necessary to consider 230 dB.
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.
Level B Harassment Risk Function (Behavioral Harassment)
The first MMPA authorization for take of marine mammals incidental
to tactical active sonar was issued in 2006 for Navy Rim of the Pacific
training exercises in Hawaii. 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 does not support the use of a step function
to estimate behavioral harassment.
Unlike step functions, acoustic risk continuum functions (which are
also called ``exposure-response functions,'' ``dose-response
functions,'' or ``stress 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. The Navy and NMFS have previously used acoustic risk
functions to estimate the probable responses of marine mammals to
acoustic exposures in the Navy FEISs on the SURTASS LFA sonar (DoN,
2001c) and the North Pacific Acoustic Laboratory experiments conducted
off the Island of Kauai (ONR, 2001). The specific risk functions used
here were also used in the MMPA regulations and FEIS for Hawaii Range
Complex (HRC), Southern California Range Complex (SOCAL), and Atlantic
Fleet Active Sonar Testing (AFAST). As discussed in the Effects
section, factors other than received level (such as distance from or
bearing to the sound source) can affect the way that marine mammals
respond; however, data to support a quantitative analysis of those (and
other factors) do not currently exist. NMFS will continue to modify
these criteria as new data becomes available.
To assess the potential effects on marine mammals associated with
active sonar used during training activity, the Navy and NMFS applied a
risk function that estimates the probability of behavioral responses
that NMFS would classify as harassment for the purposes of the MMPA
given exposure to specific received levels of MFA sonar. The
mathematical function is derived from a solution in Feller (1968) as
defined in the SURTASS LFA Sonar Final OEIS/EIS (DoN, 2001), and relied
on in the Supplemental SURTASS LFA Sonar EIS (DoN, 2007a) for the
probability of MFA sonar risk for MMPA Level B behavioral harassment
with input parameters modified by NMFS for MFA sonar for mysticetes and
odontocetes (NMFS, 2008). The same risk function and input parameters
will be applied to high frequency active (HFA) (>10 kHz) sources until
applicable data becomes available for high frequency sources.
In order to represent a probability of risk, the function should
have a value near zero at very low exposures, and a value near one for
very high exposures. One class of functions that satisfies this
criterion is cumulative probability distributions, a type of cumulative
distribution function. In selecting a particular functional expression
for risk, several criteria were identified:
The function must use parameters to focus discussion on
areas of uncertainty;
The function should contain a limited number of
parameters;
The function should be capable of accurately fitting
experimental data; and
The function should be reasonably convenient for algebraic
manipulations.
As described in U.S. Department of the Navy (2001), the
mathematical function below is adapted from a solution in Feller
(1968).
[GRAPHIC] [TIFF OMITTED] TN28FE12.001
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
[[Page 12026]]
A = Risk transition sharpness parameter = 10 (odontocetes) or 8
(mysticetes)
In order to use this function to estimate the percentage of an
exposed population that would respond in a manner that NMFS classifies
as Level B harassment, based on a given received level, the values for
B, K and A need to be identified.
B Parameter (Basement)--The B parameter is the estimated received
level below which the probability of disruption of natural behavioral
patterns, such as migration, surfacing, nursing, breeding, feeding, or
sheltering, to a point where such behavioral patterns are abandoned or
significantly altered approaches zero for the HFAS/MFAS risk
assessment. At this received level, the curve would predict that the
percentage of the exposed population that would be taken by Level B
Harassment approaches zero. For HFAS/MFAS, NMFS has determined that B =
120 dB. This level is based on a broad overview of the levels at which
many species have been reported responding to a variety of sound
sources.
K Parameter (representing the 50 percent Risk Point)--The K
parameter is based on the received level that corresponds to 50 percent
risk, or the received level at which we believe 50 percent of the
animals exposed to the designated received level will respond in a
manner that NMFS classifies as Level B Harassment. The K parameter (K =
45 dB) is based on three datasets in which marine mammals exposed to
mid-frequency sound sources were reported to respond in a manner that
NMFS would classify as Level B Harassment. There is widespread
consensus that marine mammal responses to HFA/MFA sound signals need to
be better defined using controlled exposure experiments (Cox et al.,
2006; Southall et al., 2007). The Navy is contributing to an ongoing
behavioral response study in the Bahamas that is expected to provide
some initial information on beaked whales, the species identified as
the most sensitive to MFAS. NMFS is leading this international effort
with scientists from various academic institutions and research
organizations to conduct studies on how marine mammals respond to
underwater sound exposures. Until additional data is available,
however, NMFS and the Navy have determined that the following three
data sets are most applicable for the direct use in establishing the K
parameter for the HFAS/MFAS risk function. These data sets, summarized
below, represent the only known data that specifically relate altered
behavioral responses (that NMFS would consider Level B Harassment) to
exposure to HFAS/MFAS sources.
Even though these data are considered the most representative of
the proposed specified activities, and therefore the most appropriate
on which to base the K parameter (which basically determines the
midpoint) of the risk function, these data have limitations, which are
discussed in Appendix J of the Navy's EIS for the NSWC PCD (DoN, 2009)
and summarized in the Navy's IHA application.
Calculation of K Paramenter--NMFS and the Navy used the mean of the
following values to define the midpoint of the function: (1) The mean
of the lowest received levels (185.3 dB) at which individuals responded
with altered behavior to 3 kHz tones in the SSC data set; (2) the
estimated mean received level value of 169.3 dB produced by the
reconstruction of the USS SHOUP incident in which killer whales exposed
to MFA sonar (range modeled possible received levels: 150 to 180 dB);
and (3) the mean of the 5 maximum received levels at which Nowacek et
al. (2004) observed significantly altered responses of right whales to
the alert stimuli than to the control (no input signal) is 139.2 dB
SPL. The arithmetic mean of these three mean values is 165 dB SPL. The
value of K is the difference between the value of B (120 dB SPL) and
the 50 percent value of 165 dB SPL; therefore, K = 45.
A Parameter (Steepness)--NMFS determined that a steepness parameter
(A) = 10 is appropriate for odontocetes (except harbor porpoises) and
pinnipeds and A = 8 is appropriate for mysticetes.
The use of a steepness parameter of A = 10 for odontocetes (except
harbor porpoises) for the HFAS/MFAS risk function was based on the use
of the same value for the SURTASS LFA risk continuum, which was
supported by a sensitivity analysis of the parameter presented in
Appendix D of the SURTASS/LFA FEIS (DoN, 2001c). As concluded in the
SURTASS FEIS/EIS, the value of A = 10 produces a curve that has a more
gradual transition than the curves developed by the analyses of
migratory gray whale studies (Malme et al., 1984; Buck and Tyack, 2000;
and SURTASS LFA Sonar EIS, Subchapters 1.43, 4.2.4.3 and Appendix D,
and NMFS, 2008).
NMFS determined that a lower steepness parameter (A = 8), resulting
in a shallower curve, was appropriate for use with mysticetes and HFAS/
MFAS. The Nowacek et al. (2004) dataset contains the only data
illustrating mysticete behavioral responses to a mid-frequency sound
source. A shallower curve (achieved by using A = 8) better reflects the
risk of behavioral response at the relatively low received levels at
which behavioral responses of right whales were reported in the Nowacek
et al. (2004) data. Compared to the odontocete curve, this adjustment
results in an increase in the proportion of the exposed population of
mysticetes being classified as behaviorally harassed at lower RLs, such
as those reported in and supported by the only dataset currently
available.
Basic Application of the Risk Function--The risk function is used
to estimate the percentage of an exposed population that is likely to
exhibit behaviors that would qualify as harassment (as that term is
defined by the MMPA applicable to military readiness activities, such
as the Navy's testing and research activities with HFA/MFA sonar) at a
given received level of sound. For example, at 165 dB SPL (dB re: 1
[micro]Pa rms), the risk (or probability) of harassment is defined
according to this function as 50 percent, and Navy/NMFS applies that by
estimating that 50 percent of the individuals exposed at that received
level are likely to respond by exhibiting behavior that NMFS would
classify as behavioral harassment. The risk function is not applied to
individual animals, only to exposed populations.
The data primarily used to produce the risk function (the K
parameter) were compiled from four species that had been exposed to
sound sources in a variety of different circumstances. As a result, the
risk function represents a general relationship between acoustic
exposures and behavioral responses that is then applied to specific
circumstances. That is, the risk function represents a relationship
that is deemed to be generally true, based on the limited, best-
available science, but may not be true in specific circumstances. In
particular, the risk function, as currently derived, treats the
received level as the only variable that is relevant to a marine
mammal's behavioral response. However, we know that many other
variables--the marine mammal's gender, age, and prior experience; the
activity it is engaged in during an exposure event, its distance from a
sound source, the number of sound sources, and whether the sound
sources are approaching or moving away from the animal--can be
critically important in determining whether and how a marine mammal
will respond to a sound source (Southall et al., 2007). The data that
are currently available do not allow for incorporation of these other
variables in the current risk functions; however, the risk function
represents
[[Page 12027]]
the best use of the data that are available (Figure 1).
BILLING CODE 3510-22-P
[GRAPHIC] [TIFF OMITTED] TN28FE12.002
BILLING CODE 3510-22-C
As more specific and applicable data become available for HFAS/MFAS
sources, NMFS can use these data to modify the outputs generated by the
risk function to make them more realistic. Ultimately, data may exist
to justify the use of additional, alternate, or multivariate functions.
For example, as mentioned previously, the distance from the sound
source and whether it is perceived as approaching or moving away can
affect the way an animal responds to a sound (Wartzok et al., 2003).
Estimated Exposures of Marine Mammals
Acoustical modeling provides an estimate of the actual exposures.
Detailed information and formulas to model the effects of sonar from Q-
20 sonar testing activities in the Q-20 Study Area are provided in
Appendix A, Supplemental Information for Underwater Noise Analysis of
the Navy's IHA application.
The quantitative analysis was based on conducting sonar operations
in 13 different geographical regions, or provinces. Using combined
marine mammal density and depth estimates, which are detailed later in
this section, acoustical modeling was conducted to calculate the actual
exposures. Refer to Appendix B, Geographic Description of Environmental
Provinces of the Navy's IHA application, for additional information on
provinces. Refer to Appendix C, Definitions and Metrics for Acoustic
Quantities of the Navy's IHA application, for additional information
regarding the acoustical analysis.
The approach for estimating potential acoustic effects from Q-20
test activities on cetacean species uses the methodology that the DON
developed in cooperation with NMFS for the Navy's HRC Draft EIS (DON,
2007c). The exposure analysis for behavioral response to sound in the
water uses energy flux density for Level A harassment and the methods
for risk function for Level B harassment (behavioral). The methodology
is provided here to determine the number and species of marine mammals
for which incidental take authorization is requested.
To estimate acoustic effects from the Q-20 test activities,
acoustic sources to be used were examined with regard to their
operational characteristics as described in the previous section.
Systems with an operating frequency greater than 200 kHz were not
analyzed in the detailed modeling as these signals attenuate rapidly
resulting in very short propagation distances. Based on the information
above, the Navy modeled the Q-20 sonar parameters including source
levels, ping length, the interval between pings, output frequencies,
directivity (or angle), and other characteristics based on records from
previous test scenarios and projected future testing. Additional
information on sonar systems and their associated parameters is in
Appendix A,
[[Page 12028]]
Supplemental Information for Underwater Noise Analysis of the Navy's
IHA application.
Every active sonar operation includes the potential to expose
marine animals in the neighboring waters. The number of animals exposed
to the sonar is dictated by the propagation field and the manner in
which the sonar is operated (i.e., source level, depth, frequency,
pulse length, directivity, platform speed, repetition rate). The
modeling for Q-20 test activities involving sonar occurred in five
broad steps listed below, and was conducted based on the typical RDT&E
activities planned for the Q-20 Study Area.
1. Environmental Provinces: The Q-20 Study Area is divided into 13
environmental provinces, and each has a unique combination of
environmental conditions. These represent various combinations of eight
bathymetry provinces, one Sound Velocity Profile (SVP) province, and
three Low-Frequency Bottom Loss geo-acoustic provinces and two High-
Frequency Bottom Loss classes. These are addressed by defining eight
fundamental environments in two seasons that span the variety of
depths, bottom types, sound speed profiles, and sediment thicknesses
found in the Q-20 Study Area. The two seasons encompass winter and
summer, which are the two extremes for the GOM, the acoustic
propagation characteristics do not vary significantly between the two.
Each marine modeling area can be quantitatively described as a unique
combination of these environments.
2. Transmission Loss: Since sound propagates differently in these
environments, separate transmission loss calculations must be made for
each, in both seasons. The transmission loss is predicted using
Comprehensive Acoustic Simulation System/Gaussian Ray Bundle (CASS-
GRAB) sound modeling software.
3. Exposure Volumes: The transmission loss, combined with the
source characteristics, gives the energy field of a single ping. The
energy of more than 10 hours of pinging is summed, carefully accounting
for overlap of several pings, so an accurate average exposure of an
hour of pinging is calculated for each depth increment. At more than 10
hours, the source is too far away and the energy is negligible.
Repeating this calculation for each environment in each season gives
the hourly ensonified volume, by depth, for each environment and
season. This step begins the method for risk function modeling.
4. Marine Mammal Densities: The marine mammal densities were given
in two dimensions, but using reliable peer-reviewed literature sources
(published literature and agency reports) described in the following
subsection, the depth regimes of these marine mammals are used to
project the two dimensional densities (expressed as the number of
animals per area where all individuals are assumed to be at the water's
surface) into three dimensions (a volumetric approach whereby two-
dimensional animal density incorporates depth into the calculation
estimates).
5. Exposure Calculations: Each marine mammal's three-dimensional
(3-D) density is multiplied by the calculated impact volume to that
marine mammal depth regime. This value is the number of exposures per
hour for that particular marine mammal. In this way, each marine
mammal's exposure count per hour is based on its density, depth
habitat, and the ensonified volume by depth.
The planned sonar hours were inserted and a cumulative number of
exposures was determined for the proposed action.
Based on the analysis, Q-20 sonar operations in non-territorial
waters may expose up to six species to sound likely to result in Level
B (behavioral) harassment (Table 2). They include the bottlenose
dolphin (Tursiops truncatus), Atlantic spotted dolphin (Stenella
frontalis), pantropical spotted dolphin (Stenella attenuata), striped
dolphin (Stenella coeruleoalba), spinner dolphin (Stenella
longirostris), and Clymene dolphin (Stenella clymene). No marine
mammals would be exposed to levels of sound likely to result in TTS.
The Navy requests that the take numbers of marine mammals for its IHA
reflect the exposure numbers listed in Table 2.
Table 2--Estimates of Marine Mammal Exposures From Sonar in Non-territorial Waters per Year
----------------------------------------------------------------------------------------------------------------
Level B
Marine mammal species Level A Level B (TTS) (behavioral)
----------------------------------------------------------------------------------------------------------------
Bottlenose dolphin (GOM oceanic)................................ 0 0 399
Pantropical spotted dolphin..................................... 0 0 126
Atlantic spotted dolphin........................................ 0 0 315
Spinner dolphin................................................. 0 0 126
Clymene dolphin................................................. 0 0 42
Striped dolphin................................................. 0 0 42
----------------------------------------------------------------------------------------------------------------
Potential for Long-Term Effects
Q-20 test activities will be conducted in the same general areas,
so marine mammal populations could be exposed to repeated activities
over time. However, as described earlier, this analysis assumes that
short-term non-injurious SELs predicted to cause temporary behavioral
disruptions qualify as Level B harassment. It is highly unlikely that
behavioral disruptions will result in any long-term significant
effects.
Potential for Effects on ESA-Listed Species
To further examine the possibility of whale exposures from the
proposed testing, CASSGRAB sound modeling software was used to estimate
transmission losses and received sound pressure levels (SPLs) from the
Q-20 when operating in the test area. Specifically, four radials out
towards DeSoto Canyon (which is considered an important habitat for the
ESA-listed sperm whales) were calculated. The results indicate the
relatively rapid attenuation of sound pressure levels with distance
from the source, which is not surprising given the high frequency of
the source. Below 120 dB, the risk of significant change in a
biologically important behavior approaches zero. This threshold is
reached at a distance of only 2.8 km (1.5 nm) from the source. With the
density of sperm whales being near zero in this potential zone of
influence, this calculation reinforces NMFS' conclusion that the
proposed activity is not likely to result in the take of sperm whales.
It should also be noted that DeSoto Canyon is well beyond the distance
at which sound pressure levels from the Q-20 attenuate to zero.
[[Page 12029]]
Negligible Impact and Small Numbers Analysis and Determination
Pursuant to NMFS' regulations implementing the MMPA, an applicant
is required to estimate the number of animals that will be ``taken'' by
the specified activities (i.e., takes by harassment only, or takes by
harassment, injury, and/or death). This estimate informs the analysis
that NMFS must perform to determine whether the activity will have a
``negligible impact'' on the species or stock. Level B (behavioral)
harassment occurs at the level of the individual(s) and does not assume
any resulting population-level consequences, though there are known
avenues through which behavioral disturbance of individuals can result
in population-level effects. 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
Level B harassment takes, alone, is not enough information on which to
base an impact determination. In addition to considering estimates of
the number of marine mammals that might be ``taken'' through behavioral
harassment, 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.), or
any of the other variables mentioned in the first paragraph (if known),
as well as the number and nature of estimated Level A takes, the number
of estimated mortalities, and effects on habitat.
The Navy's specified activities have been described based on best
estimates of the number of Q-20 sonar test hours that the Navy will
conduct. Taking the above into account, considering the sections
discussed below, and dependent upon the implementation of the proposed
mitigation measures, NMFS has preliminarily determined that Navy's Q-20
sonar test activities in the non-territorial waters will have a
negligible impact on the marine mammal species and stocks present in
the Q-20 Study Area.
Behavioral Harassment
As discussed in the Potential Effects of Exposure of Marine Mammals
to Sonar section and illustrated in the conceptual framework, marine
mammals can respond to HFAS/MFAS in many different ways, a subset of
which qualifies as harassment. One thing that the take estimates do not
take into account is the fact that most marine mammals will likely
avoid strong sound sources to one extent or another. Although an animal
that avoids the sound source will likely still be taken in some
instances (such as if the avoidance results in a missed opportunity to
feed, interruption of reproductive behaviors, etc.), in other cases
avoidance may result in fewer instances of take than were estimated or
in the takes resulting from exposure to a lower received level than was
estimated, which could result in a less severe response. The Navy
proposes only 420 hours of high-frequency sonar operations per year for
the Q-20 sonar testing activities, spread among 42 days with an average
of 10 hours per day, in the Q-20 Study Area. There will be no powerful
tactical mid-frequency sonar involved. Therefore, there will be no
disturbance to marine mammals resulting from MFAS systems (such as
53C). The effects that might be expected from the Navy's major training
exercises at the Atlantic Fleet Active Sonar Training (AFAST) Range,
Hawaii Range Complex (HRC), and Southern California (SOCAL) Range
Complex will not occur here. The source level of the Q-20 sonar is much
lower than the 53C series MFAS system, and high frequency signals tend
to have more attenuation in the water column and are more prone to lose
their energy during propagation. Therefore, their zones of influence
are much smaller, thereby making it easier to detect marine mammals and
prevent adverse effects from occurring.
The Navy has been conducting monitoring activities since 2006 on
its sonar operations in a variety of the Naval range complexes (e.g.,
AFAST, HRC, SOCAL) under the Navy's own protective measures and under
the regulations and LOAs. Monitoring reports based on these major
training exercises using military sonar have shown that no marine
mammal injury or mortality has occurred as a result of the sonar
operations (DoN, 2011a; 2011b).
Diel Cycle
As noted previously, many animals perform vital functions, such as
feeding, resting, traveling, and socializing on a diel cycle (24-hr
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 one day
and not recurring on subsequent days is not considered particularly
severe unless it could directly affect reproduction or survival
(Southall et al., 2007).
In the previous section, we discussed the fact that potential
behavioral responses to HFAS/MFAS that fall into the category of
harassment could range in severity. By definition, the takes by
behavioral harassment involve the disturbance of a marine mammal or
marine mammal stock in the wild by causing disruption of natural
behavioral patterns (such as migration, surfacing, nursing, breeding,
feeding, or sheltering) to a point where such behavioral patterns are
abandoned or significantly altered. In addition, the amount of time the
Q-20 sonar testing will occur is 420 hours per year in non-territorial
waters, and is spread among 42 days with an average of 10 hours per
day. Thus the exposure is expected to be sporadic throughout the year
and is localized within a specific testing site.
TTS
Based on the Navy's model and NMFS analysis, it is unlikely that
marine mammals would be exposed to sonar received levels that could
cause TTS due to the lower source level (207-212 dB re 1 [mu]Pa at 1 m)
and high attenuation rate of the HAFS signals (above 35 kHz).
Acoustic Masking or Communication Impairment
As discussed above, it is possible that anthropogenic sound could
result in masking of marine mammal communication and navigation
signals. However, masking only occurs during the time of the signal
(and potential secondary arrivals of indirect rays), versus TTS, which
occurs continuously for its duration. The Q-20 ping duration is in
milliseconds and the system is relatively low-powered making its range
of effect smaller. Therefore, masking effects from the Q-20 sonar
signals are expected to be minimal. If masking or communication
impairment were to occur briefly, it would be in the frequency range of
above 35 kHz (the lower limit of the Q-20 signals), which overlaps with
some marine mammal vocalizations; however, it would likely not mask the
entirety of any particular vocalization or communication series because
the pulse length, frequency, and duty cycle of the Q-20 sonar signal
does not perfectly mimic the characteristics of any marine mammal's
vocalizations.
PTS, Injury, or Mortality
Based on the Navy's model and NMFS analysis, it is unlikely that
PTS, injury, or mortality of marine mammals would occur from the
proposed Q-20 sonar testing activities. As discussed earlier, the lower
source level (207-212 dB re 1 [mu]Pa at 1 m) and high attenuation rate
of the HFAS signals (above 35 kHz) make
[[Page 12030]]
it highly unlikely that any marine mammals in the vicinity would be
injured (including PTS) or killed as a result of sonar exposure.
Based on the aforementioned assessment, NMFS determines that
approximately 399 bottlenose dolphins, 126 pantropical spotted
dolphins, 315 Atlantic spotted dolphins, 126 spinner dolphins, 42
Clymene dolphins, and 42 striped dolphins would be affected by Level B
behavioral harassment as a result of the proposed Q-20 sonar testing
activities. These numbers represent approximately 10.76%, 0.37%, 1.26%,
6.33%, and 0.64% of bottlenose dolphins (GOM oceanic stock),
pantropical spotted dolphins, striped dolphins, spinner dolphins, and
Clymene dolphins, respectively, of these species in the GOM region
(calculation based on NMFS 2011 US Atlantic and Gulf of Mexico Marine
Mammal Stock Assessment). The percentage of potentially affected
Atlantic spotted dolphin is unknown since there is no current
population assessment of this species in the Gulf of Mexico region.
However, based on the most recent abundance estimate published in NMFS
Atlantic and GOM SARs conducted in the northern Gulf of Mexico outer
continental shelf during fall 2000-2001 and oceanic waters during
spring/summer 2003-2004, the population was estimated at 37,611 (NMFS
2011). Using this number, it is estimated that approximately 0.84% of
Atlantic spotted dolphins would be taken by Level B behavioral
harassment from the Navy's proposed sonar test activities.
Based on the supporting analyses, which suggest that no marine
mammals will be killed, injured, or receive TTS as a result of the Q-20
sonar testing activities, and no more than a small number of any
affected species will be taken in the form of short-term Level B
behavioral harassment. Coupled with the fact that these impacts will
likely not occur in areas and times critical to reproduction, NMFS has
preliminarily determined that the taking of these species as a result
of the Navy's Q-20 sonar test will have a negligible impact on the
marine mammal species and stocks present in the Q-20 Study Area.
Subsistence Harvest of Marine Mammals
NMFS has preliminarily determined that the total taking of marine
mammal species or stocks from the Navy's Q-20 sonar testing in the Q-20
Study Area would not have an unmitigable adverse impact on the
availability of the affected species or stocks for subsistence uses,
since there are no such uses in the specified area.
Endangered Species Act (ESA)
Based on the analysis of the Navy Marine Resources Assessment (MRA)
data on marine mammal distributions, there is near zero probability
that sperm whale will occur in the vicinity of the proposed Q-20 test
area. No other ESA-listed marine mammal is expected to occur in the
vicinity of the test area. In addition, acoustic modeling analysis
indicates that none of the ESA-listed marine mammal species would be
exposed to levels of sound that would constitute a ``take'' under the
MMPA, due to the low source level and high attenuation rates of the Q-
20 sonar signal. Therefore, the Navy has determined that ESA-listed
species are not likely to be adversely affected as the result of the
Navy's proposed Q-20 testing activities and has requested concurrence
from NMFS.
National Environmental Policy Act (NEPA)
In 2009, the Navy prepared a Final Environmental Impact Statement/
Overseas Environmental Impact Statement for the NSWC PCD Mission
Activities (FEIS/OEIS), and NMFS subsequently adopted the FEIS/OEIS for
its rule governing the Navy's RDT&E activities in the NSWC PCD Study
Area. The currently proposed Q-20 sonar testing activities are similar
to the sonar testing activities described in the FEIS/OEIS for NSWC PCD
mission activities. NMFS will prepare an Environmental Assessment to
reflect these additional Q-20 sonar test activities.
Dated: February 23, 2012.
James H. Lecky,
Director, Office of Protected Resources, National Marine Fisheries
Service.
[FR Doc. 2012-4695 Filed 2-27-12; 8:45 am]
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