Takes of Marine Mammals Incidental to Specified Activities; Taking Marine Mammals Incidental to Seismic Surveys in Cook Inlet, Alaska, 29161-29189 [2015-12091]
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Vol. 80
Wednesday,
No. 97
May 20, 2015
Part II
Department of Commerce
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National Oceanic and Atmospheric Administration
Takes of Marine Mammals Incidental to Specified Activities; Taking Marine
Mammals Incidental to Seismic Surveys in Cook Inlet, Alaska; Notices
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Federal Register / Vol. 80, No. 97 / Wednesday, May 20, 2015 / Notices
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XD830
Takes of Marine Mammals Incidental to
Specified Activities; Taking Marine
Mammals Incidental to Seismic
Surveys in Cook Inlet, Alaska
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; issuance of an incidental
harassment authorization.
AGENCY:
NMFS is issuing an Incidental
Harassment Authorization in response
to a request from SAExploration Inc.
(SAE) for authorization to take marine
mammals incidental to an oil and gas
exploration seismic survey program in
Cook Inlet, Alaska between May 13,
2015 and May 12, 2016.
DATES: Effective: May 13, 2015 through
May 12, 2016.
ADDRESSES: Electronic copies of the
IHA, application, and associated
Environmental Assessment (EA) and
Finding of No Significant Impact
(FONSI) may be obtained by writing to
Jolie Harrison, Division Chief, Permits
and Conservation Division, Office of
Protected Resources, National Marine
Fisheries Service, 1315 East West
Highway, Silver Spring, MD 20910,
telephoning the contact listed below
(see FOR FURTHER INFORMATION CONTACT),
or visiting the internet at: 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: Sara
Young, Office of Protected Resources,
NMFS, (301) 427–8401.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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Background
Sections 101(a)(5)(A) and (D) of the
MMPA (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce to allow,
upon request, the incidental, but not
intentional, taking of small numbers of
marine mammals by U.S. citizens who
engage in a specified activity (other than
commercial fishing) within a specified
geographical region if certain findings
are made and either regulations are
issued or, if the taking is limited to
harassment, a notice of a proposed
authorization is provided to the public
for review.
An authorization for incidental
takings shall be granted if NMFS finds
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that the taking will have a negligible
impact on the species or stock(s), will
not have an unmitigable adverse impact
on the availability of the species or
stock(s) for subsistence uses (where
relevant), and if the permissible
methods of taking and requirements
pertaining to the mitigation, monitoring
and reporting of such takings are set
forth. NMFS has defined ‘‘negligible
impact’’ in 50 CFR 216.103 as ‘‘an
impact resulting from the specified
activity that cannot be reasonably
expected to, and is not reasonably likely
to, adversely affect the species or stock
through effects on annual rates of
recruitment or survival.’’
Except with respect to certain
activities not pertinent here, the MMPA
defines ‘‘harassment’’ as: Any act of
pursuit, torment, or annoyance which (i)
has the potential to injure a marine
mammal or marine mammal stock in the
wild [Level A harassment]; or (ii) has
the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment].
Summary of Request
On October 28, 2014, we received a
request from SAE for authorization to
take marine mammals incidental to
seismic surveys in Cook Inlet, Alaska.
After further correspondence and
revisions by the applicant, we
determined that the application was
adequate and complete on January 12,
2015. On March 20, 2015, NMFS
published a notice in the Federal
Register of our proposal to issue an IHA
with preliminary determinations (80 FR
14913). The filing of the notice initiated
a 30-day public comment period. The
comments and our responses are
discussed later in this document.
SAE proposes to conduct oil and gas
exploration seismic surveys. The
activity will occur between May 13,
2015 and May 12, 2016, for a period of
160 days. The following specific aspects
of the activity are likely to result in the
take of marine mammals: Operation of
seismic airguns in arrays of 440 in3 and
1,760 in3. Take, by Level B Harassment
only, of individuals of beluga whale,
humpback whale, minke whale, gray
whale, harbor porpoise, Dall’s porpoise,
killer whale, harbor seal, and Steller sea
lion is anticipated to result from the
specified activity.
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Description of the Specified Activity
Overview
SAE plans to conduct 3D seismic
surveys over multiple years in the
marine waters of both upper and lower
Cook Inlet. This authorization will cover
activities occurring between May 13,
2015 and May 12, 2016. The ultimate
survey area is divided into two units
(upper and lower Cook Inlet). The total
potential survey area is 3,934 square
kilometers (1,519 square miles);
however, only a portion (currently
unspecified) of this area will ultimately
be surveyed, and no more than 777
square kilometers (300 square miles) in
a given year. The exact location of
where the 2015 survey will be
conducted is not known at this time,
and probably will not be known until
late spring 2015 when SAE’s clients
have finalized their data acquisition
needs.
The components of the project
include laying recording sensors (nodes)
on the ocean floor, operating seismic
source vessels towing active air gun
arrays, and retrieval of nodes. There will
also be additional boat activity
associated with crew transfer, recording
support, and additional monitoring for
marine mammals. The primary seismic
source for offshore recording consists of
a 2 × 880-cubic-inch tri-cluster array for
a total of 1,760-cubic-inches (although a
440-cubic-inch array may be used in
very shallow water locations as
necessary). Each of the arrays will be
deployed in a configuration outlined in
Appendix A of the application. The
arrays will be centered approximately
15 meters (50 feet) behind the source
vessel stern, at a depth of 4 meters (12
feet), and towed along predetermined
source lines at speeds between 7.4 and
9.3 kilometers per hour (4 and 5 knots).
Two vessels with full arrays will be
operating simultaneously in an
alternating shot mode; one vessel
shooting while the other is recharging.
Shot intervals are expected to be about
16 seconds for each array resulting in an
overall shot interval of 8 seconds
considering the two alternating arrays.
Operations are expected to occur 24
hours a day, with actual daily shooting
to total about 12 hours. An acoustical
positioning (or pinger) system will be
used to position and interpolate the
location of the nodes. A vessel-mounted
transceiver calculates the position of the
nodes by measuring the range and
bearing from the transceiver to a small
acoustic transponder fitted to every
third node. The transceiver uses sonar
to interrogate the transponders, which
respond with short pulses that are used
in measuring the range and bearing.
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Several offshore vessels will be required
to support recording, shooting, and
housing in the marine and transition
zone environments. Exact vessels to be
used have not been determined.
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Dates and Duration
The request for incidental harassment
authorization is primarily for the 2015
Cook Inlet open water season. The plan
is to conduct seismic surveys in the
Upper Cook unit sometime between
May 13, 2015 through May 12, 2016.
The northern border of the seismic
survey area depicted in Figure 1 takes
into account the restriction that no
activity occur between April 15 to
October 15 in waters within 16
kilometers (10 miles) of the Susitna
Delta (defined as the nearshore area
between the mouths of the Beluga and
the Little Susitna rivers). A small wedge
of the upper Cook unit falls within 16
kilometers of the Beluga River mouth,
but survey here will occur after October
15, taking into account any timing
restrictions with nearshore beluga
habitat. The seismic acquisition in
lower Cook unit will initially begin in
late August or mid-September, and run
until December 15 taking into account
any self-imposed location/timing
restrictions to avoid encounters with sea
otters or Steller’s eiders. The exact
survey dates in a given unit will depend
on ice conditions, timing restrictions,
and other factors. If the upper Cook Inlet
seismic surveys are delayed by spring
ice conditions, some survey may occur
in lower Cook Inlet from March to May
to maximize use of the seismic fleet.
Actual data acquisition is expected to
occur for only 2 to 3 hours at a time
during each of the 3 to 4 daily slack
tides. Thus, it is expected that the air
guns will operate an average of about 8
to 10 total hours per day. It is estimated
that it will take 160 days to complete
both the upper and lower Cook units,
and that no more than 777 square
kilometers (300 square miles) of survey
area will be shot in 2015.
Specified Geographic Region
The area of Cook Inlet that SAE plans
to operate in has been divided into two
subsections: Upper and Lower Cook
Inlet. Upper Cook (2,126 square
kilometers; 821 square miles) begins at
the line delineating Cook Inlet beluga
whale (Delphinapterus leucas) Critical
Habitat Area 1 and 2, south to a line
approximately 10 kilometers (6 miles)
south of both the Lower Cook (1,808
square kilometer; 698 square mile)
begins east of Kalgin Island and running
along the east side of lower Cook Inlet
to Anchor Point (Figure 2 in SAE
application).
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Detailed Description of Activities
The Notice of Proposed IHA (80 FR
14913, March 20, 2015) contains a full
detailed description of the 3D seismic
survey, including the recording system,
sensor positioning, and seismic source.
That information has not changed and is
therefore not repeated here.
Comments and Responses
A Notice of Proposed IHA was
published in the Federal Register on
March 20, 2015 (80 FR 14913) for public
comment. During the 30-day public
comment period, NMFS received four
comment letters from the following: The
Natural Resource Defense Council
(NRDC); the Marine Mammal
Commission (MMC); Furie Operating
Alaska LLC (Furie); and one private
citizen.
All of the public comment letters
received on the Notice of Proposed IHA
(80 FR 14913, March 20, 2015) are
available on the internet at: https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm. Following is a summary
of the public comments and NMFS’
responses.
Comment 1: One private citizen
requested that we deny issuance of the
IHA because marine mammals would be
killed as a result of the survey.
Response: Extensive analysis of the
proposed 3D seismic survey was
conducted in accordance with the
MMPA, Endangered Species Act (ESA),
and National Environmental Policy Act
(NEPA). Pursuant to those statutes, we
analyzed the impacts to marine
mammals (including those listed as
threatened or endangered under the
ESA), their habitat (including critical
habitat designated under the ESA), and
to the availability of marine mammals
for taking for subsistence uses. The
MMPA analyses revealed that the
activities would have a negligible
impact on affected marine mammal
species or stocks and would not have an
unmitigable adverse impact on the
availability of marine mammals for
taking for subsistence uses. The ESA
analysis concluded that the activities
likely would not jeopardize the
continued existence of ESA-listed
species or destroy or adversely modify
designated critical habitat. The NEPA
analysis concluded that there would not
be a significant impact on the human
environment. Moreover, this activity is
not expected to result in the death of
any marine mammal species, and no
such take is authorized.
Comment 2: Furie supports issuance
of this IHA in a timely manner and urge
NMFS to recognize the benefits of
seismic surveys and subsequent
development of energy resources.
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Response: After careful evaluation of
all comments and the data and
information available regarding
potential impacts to marine mammals
and their habitat and to the availability
of marine mammals for subsistence
uses, NMFS has issued the final
authorization to SAE to take marine
mammals incidental to conducting a 3D
seismic survey program in Cook Inlet for
the period May 13, 2015 through May
12, 2016.
Comment 3: The MMC recommends
that NMFS defer issuance of the IHA
until such time as NMFS can, with
reasonable confidence, support a
conclusion that the activities would
affect no more than a small number of
Cook Inlet beluga whales and have no
more than a negligible impact on the
population. The MMC recommends that
NMFS defer issuance until we have
better information on the cause or
causes of ongoing decline of the
population and a reasonable basis for
determining that authorizing additional
takes would not contribute to or
exacerbate that decline. The MMC
continues to believe that any activity
that may contribute to or that may
worsen the observed decline should not
be viewed as having a negligible impact
on the population. The NRDC states that
NMFS failed to meet both the ‘‘small
numbers’’ and ‘‘negligible impact’’
standards.
Response: In accordance with our
implementing regulations at 50 CFR
216.104(c), we use the best available
scientific evidence to determine
whether the taking by the specified
activity within the specified geographic
region will have a negligible impact on
the species or stock and will not have
an unmitigable adverse impact on the
availability of such species or stock for
subsistence uses. Based on the scientific
evidence available, NMFS determined
that the impacts of the 3D seismic
survey program, which are primarily
acoustic in nature, would meet these
standards. Moreover, SAE proposed and
NMFS has required in the IHA a
rigorous mitigation plan to reduce
impacts to Cook Inlet beluga whales and
other marine mammals to the lowest
level practicable, including measures to
power down or shutdown airguns if any
beluga whale is observed approaching
or within the Level B harassment zone
and restricting activities within a 10 mi
(16 km) radius of the Susitna Delta from
April 15 through October 15, which is
an important area for beluga feeding and
calving in the spring and summer
months. This shutdown measure is
more restrictive than the standard
shutdown measures typically applied,
and combined with the Susitna Delta
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exclusion (minimizing adverse effects to
foraging), is expected to reduce both the
scope and severity of potential
harassment takes, ensuring that there
are no energetic impacts from the
harassment that would adversely affect
reproductive rates or survivorship.
Our analysis indicates that issuance of
this IHA will not contribute to or
worsen the observed decline of the Cook
Inlet beluga whale population.
Additionally, the ESA Biological
Opinion determined that the issuance of
an IHA is not likely to jeopardize the
continued existence of the Cook Inlet
beluga whales or the western distinct
population segment of Steller sea lions
or destroy or adversely modify Cook
Inlet beluga whale critical habitat. The
Biological Opinion also outlined Terms
and Conditions and Reasonable and
Prudent Measures to reduce impacts,
which have been incorporated into the
IHA. Therefore, based on the analysis of
potential effects, the parameters of the
seismic survey, and the rigorous
mitigation and monitoring program,
NMFS determined that the activity
would have a negligible impact on the
population.
Moreover, the seismic survey would
take only small numbers of marine
mammals relative to their population
sizes. The number of belugas likely to be
taken represent less than 9.6% of the
population. As described in the
proposed IHA Federal Register notice,
NMFS used a method that incorporates
density of marine mammals overlaid
with the anticipated ensonified area to
calculate an estimated number of takes
for belugas, which was estimated to be
less than 10% of the stock abundance,
which NMFS considers small. In
addition to this quantitative evaluation,
NMFS has also considered qualitative
factors that further support the ‘‘small
numbers’’ determination, including: (1)
The seasonal distribution and habitat
use patterns of Cook Inlet beluga
whales, which suggest that for much of
the time only a small portion of the
population would be accessible to
impacts from SAE’s activity, as most
animals are concentrated in upper Cook
Inlet; and (2) the mitigation
requirements, which provide spatiotemporal limitations that avoid impacts
to large numbers of animals feeding and
calving in the Susitna Delta and limit
exposures to sound levels associated
with Level B harassment. Based on all
of this information, NMFS determined
that the number of beluga whales likely
to be taken is small. See response to
Comment 5 and our small numbers
analysis later in this document for more
information about the small numbers
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determination for beluga whales and the
other marine mammal species.
Comment 4: The MMC recommends
that NMFS develop a policy that sets
forth clear criteria and/or thresholds for
determining what constitutes ‘‘small
numbers’’ and ‘‘negligible impact’’ for
the purpose of authorizing incidental
takes of marine mammals. The MMC
understands that NMFS has been
working on developing a policy and
would welcome an opportunity to
discuss this policy further before it is
finalized.
Response: NMFS is in the process of
developing both a clearer policy to
outline the criteria for determining what
constitutes ‘‘small numbers’’ and an
improved analytical framework for
determining whether an activity will
have a ‘‘negligible impact’’ for the
purpose of authorizing takes of marine
mammals. We fully intend to engage the
MMC in these processes at the
appropriate time.
Comment 5: The NRDC pointed by
reference to the other proposed
activities in Cook Inlet during the 2015
open water season. The NRDC and the
MMC both note that NMFS must
address the cumulative effects of
activities in Cook Inlet on Cook Inlet
beluga whales and whether the
cumulative impacts of all the activities
are having ‘‘either individually or in
combination’’ a greater than negligible
impact on marine mammals.
Response: Neither the MMPA nor
NMFS’ implementing regulations
specify how to consider other activities
and their impacts on the same
populations when conducting a
negligible impact analysis. However,
consistent with the 1989 preamble for
NMFS’ implementing regulations (54 FR
40338, September 29, 1989), the impacts
from other past and ongoing
anthropogenic activities are
incorporated into the negligible impact
analysis via their impacts on the
environmental baseline (e.g., as
reflected in the density/distribution and
status of the species, population size
and growth rate, and ambient noise).
In addition, cumulative effects were
addressed in the EA and Biological
Opinion prepared for this action. The
cumulative effects section of the EA has
been expanded from the draft EA to
discuss potential effects in greater
detail. These documents, as well as the
Alaska Marine Stock Assessments and
the most recent abundance estimate for
Cook Inlet beluga whales (Shelden et
al., 2015, are part of NMFS’
Administrative Record for this action,
and provided the decision maker with
information regarding other activities in
the action area that affect marine
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mammals, an analysis of cumulative
impacts, and other information relevant
to the determination made under the
MMPA.
Comment 6: The NRDC states that
NMFS failed to account for survey
duration in the estimation of beluga
whale takes and that NMFS based
beluga takes using a predictive habitat
density model (Goetz et al., 2012) that
is based on data from summer months
and confined to summer distribution
when belugas are generally concentrated
in the Upper Inlet, even though activity
could occur year round.
Response: The numerical estimation
of take for beluga whales does consider
survey duration in the calculation. The
Goetz et al 2012 model is the best
available data for beluga density in Cook
Inlet. The method used by NMFS to
estimate take uses the best available
data to most accurately estimate the
number of belugas taken. This is done
by multiplying the density of the area
surveyed on a given day by the area
ensonified on that day of surveying to
yield the number of belugas that were
likely exposed during that day of
surveying. This is then added to the
next day of surveying and so forth in an
additive model until the number of 30
belugas is reached. If the number of 30
belugas is reached using this calculation
before SAE has completed their 160
days of proposed surveying, survey
activity must cease. Additionally, if they
finish their 160 days without reaching
the limit of 30 belugas their activity
must still cease. The model, by being
additive in nature for each day of
surveying, accounts for the duration of
the survey, as well as capturing a more
specific density value than using an
Inlet-wide density estimate.
Moreover, the model (or other
numerical methods for estimating take)
does not take into consideration the
rigorous mitigation protocols that will
be implemented by SAE to reduce the
number of actual Level B harassment
takes of Cook Inlet beluga whales. As
mentioned previously, the IHA contains
a condition restricting SAE’s airgun
operations within 10 mi (16 km) of the
mean higher high water line of the
Susitna Delta from April 15 through
October 15. During this time, a
significant portion of the Cook Inlet
beluga whale population occurs in this
area for feeding and calving. This
setback distance includes the entire 160
dB radius of 5.9 mi (9.5 km) predicted
for the full airgun array plus an
additional 4.1 mi (6.5 km) of buffer, thus
reducing the number of animals that
may be exposed to Level B harassment
thresholds. SAE is also required to shut
down the airguns if any beluga whale is
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sighted approaching or entering the
Level B harassment zone to avoid take.
NMFS combined use of the National
Marine Mammal Laboratory (NMML)
model, which we determined to be the
best available data upon which to base
density estimates, with consideration of
all of the mitigation measures required
to be implemented to authorize 30
beluga whale takes. This approach is
reasonable and does not contradict
available science and data of beluga
whale distribution and local abundance
during the period of operations.
Comment 7: The NRDC states that in
the case of marine mammals other than
beluga whales, NMFS repeated past
errors associated with its use of raw
NMML survey data. Errors in the
density calculations include the failure
to incorporate correction factors for
missed marine mammals in the analysis
and the failure to fully account for
survey duration by multiplying
densities (which are calculated on an
hourly basis) by the number of survey
days but not the number of hours in a
day.
Response: Correction factors for
marine mammal surveys, with the
exception of beluga whales, are not
available for Cook Inlet. The primary
purpose and focus of the NMFS aerial
surveys in Cook Inlet for the past decade
has been to monitor the beluga whale
population. Although incidental
observations of other marine mammals
are noted during these surveys, they are
focused on beluga whales. With the
exception of the beluga whale, no
detailed statistical analysis of Cook Inlet
marine mammal survey results has been
conducted, and no correction factors
have been developed for Cook Inlet
marine mammals. The only published
Cook Inlet correction factor is for beluga
whales. Developing correction factors
for other marine mammals would have
required different survey data collection
and consideration of unavailable data
such as Cook Inlet sight ability,
movement patterns, tidal correlations
and detailed statistical analyses. For
example, other marine mammal
numbers are often rounded to the
nearest 10 or 100 during the NMFS
aerial survey; resulting in unknown
observation bias. Therefore, the data
from the NMFS surveys are the best
available and number of animals taken
are still likely overestimated because of
the assumption that there is a 100%
turnover rate of marine mammals each
day.
Survey duration was appropriately
considered in the estimations by
multiplying density by area of
ensonification by number of survey
days. NMFS does not calculate takes on
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an hourly basis, and, additionally, the
multiple hours surveyed within a day
are reflected in the area of
ensonification, which considers the
distance they can move within a day
and is therefore larger than what would
be covered in one hour. Additionally, as
NMFS has used the density estimate
from NMFS aerial surveys, multiplied
by the area ensonified per day,
multiplied by the number of days, this
calculation produces the number
instances of exposure during the survey.
This is likely an overestimate of
individuals taken by Level B
harassment, as a single individual can
be exposed on multiple days over the
course of the survey, especially when a
small patch of area is shot over a
duration of five days. While protected
species observers (PSOs) cannot detect
every single animal within the Level B
harassment zone, monitoring reports
from similar activities indicate that
sightings did not exceed anticipated
estimates.
Comment 8: The NRDC commented
that NMFS underestimated the size of
SAE’s impact area by: (1) Using an
outdated and incorrect threshold for
behavioral take; and (2) disregarding the
best available evidence on the potential
for temporary and permanent threshold
shift on mid- and high-frequency
cetaceans and on pinnipeds.
Response: The comment that NMFS
uses an outdated and incorrect
threshold for behavioral takes does not
include any specific recommendations.
NMFS uses 160 dB (rms) as the
exposure level for estimating Level B
harassment takes for most species in
most cases. This threshold was
established for underwater impulse
sound sources based on measured
avoidance responses observed in whales
in the wild. Specifically, the 160 dB
threshold was derived from data for
mother-calf pairs of migrating gray
whales (Malme et al., 1983, 1984) and
bowhead whales (Richardson et al.,
1985, 1986) responding to seismic
airguns (e.g., impulsive sound source).
We acknowledge there is more recent
information bearing on behavioral
reactions to seismic airguns, but those
data only illustrate how complex and
context-dependent the relationship is
between the two. See 75 FR 49710,
49716 (August 13, 2010) (IHA for Shell
seismic survey in Alaska). Accordingly,
it is not a matter of merely replacing the
existing threshold with a new one.
NOAA is working to develop more
sophisticated draft guidance for
determining impacts from acoustic
sources, including information for
determining Level B harassment
thresholds. Due to the complexity of the
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task, any guidance will require a
rigorous review that includes internal
agency review, public notice and
comment, and additional external peer
review before any final product is
published. In the meantime, and taking
into consideration the facts and
available science, NMFS determined it
is reasonable to use the 160 dB
threshold for estimating takes of marine
mammals in Cook Inlet by Level B
harassment. However, we discuss the
science on this issue qualitatively in our
analysis of potential effects to marine
mammals.
The comment that NMFS disregarded
the best available evidence on the
potential for temporary and permanent
threshold shift on mid- and highfrequency cetaceans and on pinnipeds
does not contain any specific
recommendations. We acknowledge
there is more recent information
available bearing on the relevant
exposure levels for assessing temporary
and permanent hearing impacts. (See
NMFS’ Federal Register notice (78 FR
78822, December 27, 2013) for NMFS’
draft guidance for assessing the onset of
permanent and temporary threshold
shift.) Again, NMFS will be issuing
guidance, but that process is not
complete, so we did not use it to assign
new thresholds for calculating take
estimates for hearing impacts. However,
we did consider the information, and it
suggests the current 180 and 190 dB
thresholds are appropriate and that they
likely overestimate potential for hearing
impacts. See 75 FR 49710, 49715, 49724
(August 13, 2010) (IHA for Shell seismic
survey in Alaska; responses to comment
8 and comment 27). Moreover, the
required mitigation is designed to
ensure there are no exposures at levels
thought to cause hearing impairment,
and, for several of the marine mammal
species in the project area, mitigation
measures are designed to reduce or
eliminate exposure to Level B
harassment thresholds.
Comment 9: The NRDC comments
that the proposed mitigation measures
fail to meet the MMPA’s ‘‘least
practicable adverse impact’’ standard.
The NRDC provides a list of
approximately eight measures that
NMFS ‘‘failed to consider or adequately
consider.’’
Response: NMFS provided a detailed
discussion of proposed mitigation
measures and the MMPA’s ‘‘least
practicable impact’’ standard in the
notice of the proposed IHA (80 FR
14913, March 20, 2015), which are
repeated in the ‘‘Mitigation’’ section of
this notice. The measures that NMFS
allegedly failed to consider or
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adequately consider are identified and
discussed below:
(1) Field testing and use of alternative
technologies, such as vibroseis and
gravity gradiometry, to reduce or
eliminate the need for airguns and
delaying seismic acquisition in higher
density areas until the alternative
technology of marine vibroseis becomes
available: SAE requested takes of marine
mammals incidental to the seismic
survey operations described in the IHA
application, which identified airgun
arrays as the technique SAE would
employ to acquire seismic data. It would
be inappropriate for NMFS to change
the specified activity and it is beyond
the scope of the request for takes
incidental to SAE’s operation of airguns
and other active acoustic sources.
SAE knows of no current technology
scaled for industrial use that is reliable
enough to meet the environmental
challenges of operating in Cook Inlet.
SAE is aware that many prototypes are
currently in development, and may
ultimately incorporate these new
technologies into their evaluation
process as they enter commercial
viability. However, none of these
technologies are currently ready for use
on a large scale in Cook Inlet. As this
technology is developed, SAE will
evaluate its utility for operations in the
Cook Inlet environment.
(2) Required use of the lowest
practicable source level in conducting
airgun activity: SAE determined that the
1760 in3 array provides the data
required for SAE’s operations.
(3) Seasonal exclusions around river
mouths, including early spring (preApril 14) exclusions around the Beluga
River and Susitna Delta, and avoidance
of other areas that have a higher
probability of beluga occurrence: NMFS
has required a 10 mile (16 km)
exclusion zone around the Susitna Delta
(which includes the Beluga River) in
this IHA. This mitigation mirrors a
measure in the Incidental Take
Statement for the 2012 and 2013
Biological Opinions. Seismic survey
operations involving the use of airguns
will be prohibited in this area between
April 15 and October 15. In both the
MMPA and ESA analysis, NMFS
determined that this date range is
sufficient to protect Cook Inlet beluga
whales and the critical habitat in the
Susitna Delta. While data indicate that
belugas may use this part of the inlet
year round, peak use occurs from early
May to late September. NMFS added a
2-week buffer on both ends of this peak
usage period to add extra protection to
feeding and calving belugas. (In
addition, the Alaska Department of Fish
and Game (ADF&G) prohibits the use of
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airguns within 1 mi (1.6 km) of the
mouth of any stream listed by the
ADF&G on the Catalogue of Waters
Important for the Spawning, Rearing, or
Migration of Anadromous Fishes. See
additional explanation in ‘‘Mitigation
Measures Considered but not Required’’
section, later in this document.)
(4) Limitation of the mitigation airgun
to the longest shot interval necessary to
carry out its intended purpose: This
general comment contained no specific
recommendations. SAE requires shot
intervals of 50m at a speed of 4–5 knots
to obtain the information from their
survey. However NMFS has added a
mitigation measure that SAE reduce the
shot interval for the mitigation gun to
one shot per minute.
(5) Immediate suspension of airgun
activity, pending investigation, if any
beluga strandings occur within or
within an appropriate distance of the
survey area. The IHA requires SAE to
immediately cease activities and report
unauthorized takes of marine mammals,
such as live stranding, injury, serious
injury, or mortality. NMFS will review
the circumstances of SAE’s
unauthorized take and determine if
additional mitigation measures are
needed before activities can resume to
minimize the likelihood of further
unauthorized take and to ensure MMPA
compliance. SAE may not resume
activities until notified by NMFS.
Separately the IHA includes measures if
injured or dead marine mammals are
sighted and the cause cannot be easily
determined. In those cases, NMFS will
review the circumstances of the
stranding event while SAE continues
with operations.
(6) Establishment of a larger exclusion
zone for beluga whales that is not
predicated on the detection of whale
aggregations or cow-calf pairs: Both the
proposed IHA notice and the issued IHA
contain a requirement for SAE to delay
the start of airgun use or shutdown the
airguns if a beluga whale is visually
sighted or detected by passive acoustic
monitoring approaching or within the
160-dB disturbance zone until the
animal(s) are no longer present within
the 160-dB zone. The measure applies to
the sighting of any beluga whale, not
just sightings of groups or cow-calf
pairs.
Comment 10: The MMC suggests
additional mitigation measures are used
including: (1) Aerial surveys, (2) passive
acoustic monitoring, as well as (3) a 30
minute post-activity monitoring period.
Response: NMFS provided a detailed
discussion of proposed mitigation
measures and the MMPA’s ‘‘least
practicable impact’’ standard in the
notice of the proposed IHA (80 FR
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14913, March 20, 2015), which are
repeated in the ‘‘Mitigation’’ section of
this notice. The measures that NMFS
allegedly failed to consider or
adequately consider are identified and
discussed below:
(1) Use of advance aerial surveys to
redirect activity is not required for this
action. Aerial surveys for this project
could be used for monitoring the
disturbance zone to the 160dB level
(6.83 km). However, exposures that
occur in this zone, or Level B takes, are
already accounted for in the take
estimation section below. Visual
observers, which are already known to
be effective in this environment, will
adhere to strict standards for preventing
animals from entering the 180dB/190dB
injury exclusion zone, as well as
monitoring for animals that may be
traveling in the direction of or
approaching the injury exclusion zone.
The prohibitive cost of daily aerial
surveys for a survey area of only
777km2, combined with the limited
added value given the general
effectiveness of vessel and land-based
observers, and considering the fact that
we believe that the activity will have a
negligible impact even in the absence of
mitigation make the suite of mitigation
measures we have included adequate to
achieve the least practicable adverse
impact.
(2) The passive acoustic monitoring
plan for Apache Alaska Corporation’s
2012 survey anticipated the use of a
bottom-mounted telemetry buoy to
broadcast acoustic measurements using
a radio-system link back to a monitoring
vessel. Although a buoy was deployed
during the first week of surveying under
the 2012 IHA, it was not successful.
Upon deployment, the buoy
immediately turned upside down due to
the strong current in Cook Inlet. After
retrieval, the buoy was not redeployed
and the survey used a single omnidirectional hydrophone lowered from
the side of the mitigation vessel. During
the entire 2012 survey season, Apache’s
PAM equipment yielded only six
confirmed marine mammal detections,
one of which was a Cook Inlet beluga
whale. The single Cook Inlet beluga
whale detection did not, however, result
in a shutdown procedure.
Additionally, Joint Base ElmendorfFort Richardson, the National Marine
Mammal Laboratory, and Alaska
Department of Fish & Game conducted
a 2012 study (Gillespie et al., 2013) to
determine if beluga whale observations
at the mouth of Eagle River
corresponded with acoustic detections
received by a PAMBuoy data collection
system. The PAMBuoy data collection
system was deployed in the mouth of
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Eagle River from 12–31 August 2012.
This study was a trial period conducted
with one hydrophone at the mouth of
the river. Overall, it was successful in
detecting beluga whale echolocation
clicks and whistles, but came with
several limitations:
• The PAM system was able to
reliably detect all whales approaching
or entering the river but still performs
less well than a human observer;
• Sounds from vessels in Cook Inlet
(e.g. vessel noise) have a large chance of
interfering with detections from PAM.
The mouth of Eagle River has very little
vessel traffic, which is likely why the
study was successful there and not
likely to be successful in Cook Inlet;
• PAMbouys could be a navigational
hazard in Cook Inlet for commercial,
subsistence, and sport fishing, as well as
the commercial vessel traffic traveling
through Cook Inlet;
• The limited testing in a very small
area should not become the new
standard of monitoring in the entire
Cook Inlet. The tide, vessel traffic,
bathymetry, and substrate of Cook Inlet
are far more complex than the study
area;
• It appears the hydrophone must be
hardwired to the shore which is not
practical for mobile marine seismic
operations;
• Currently, deployment of the
system is done by walking tripods onto
the mudflats. This is not feasible for the
vast majority of the SAE project area.
Walking onto the mudflats in parts of
Cook Inlet also poses a safety risk;
• The study found considerable
investment would be necessary to
develop an ice and debris proof
mounting system. Other issues with
hydrophone configuration include: At
extreme low tides, the hydrophone was
uncovered and therefore not usable; the
hydrophone had to be located in such
a position so that it could be
occasionally visually inspected;
hydrophone battery supply has to
constantly be checked; the costs and
practicalities of long-term hydrophone
mounting and data transmission have
not been determined.; and only one
hydrophone was tested, and SAE would
need several hydrophones;
• Observer sightings and acoustic
detections of belugas generally
corresponded with one another. Thus
PAMBuoys would be simply
duplicating PSO and aerial efforts;
• The wireless modem that transmits
the acoustic data to the ‘‘base station’’
was only tested to 3.2 km; and
• The study did not conclude
anything about the detection range of
the system, except that it was greater
than 400 m.
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NMFS has been made aware of an
over-the-side hydrophone that has
successfully detected belugas in Eagle
River, Alaska. Upon beginning
operations, SAE has 30 days to acquire
a hydrophone that covers a frequency
range of 0.1–160 kHz to allow detecting
both social and echolocation signals,
with a system sensitivity in the range
¥165 to ¥185 dB re1 V/mPa, and floor
noise spectra similar to Beaufort Sea
State 0. SAE will use this hydrophone
during nighttime ramp-ups from the
mitigation airgun to detect beluga
whales, humpbacks, and Steller sea
lions that may be within the 160dB
disturbance zone.
(3) A post-activity monitoring period
of 30 minutes has been added as a
requirement for this activity. This
monitoring period after the cessation of
airgun operations can provide useful
observations to compare the behavior
and abundance of animals during
different scenarios of various noise
levels. This change has been noted in
the Authorization text.
Comment 11: The MMC notes that
NMFS is reviewing two other IHA
applications for proposed seismic
surveys in Cook Inlet in 2015 and that
it is not clear whether these applications
are seeking separate authorizations for
some or all of the same activities. NMFS
needs to adopt policies and institute
procedures to ensure that separate
applications to conduct essentially the
same activities in the same areas are
considered more holistically. If indeed
the applicants are proposing to conduct
multiple seismic surveys within the
same area, it would increase the
numbers of marine mammals taken and
expose beluga whales and other marine
mammals to unnecessary, avoidable
risks. Section 101(a)(5)(D)(ii)(I) of the
MMPA directs NMFS to structure IHAs
so that they prescribe ‘‘other means of
effecting the least practicable impact on
such species or stock and its habitat.’’
Allowing multiple operators to obtain
separate IHAs to conduct duplicative
surveys is inconsistent with that
mandate. Data sharing and collaboration
is critical in habitat areas used by
endangered populations, such as Cook
Inlet beluga whales. The MMC
recommends that NMFS encourage SAE
and other applicants proposing to
conduct seismic surveys in Cook Inlet in
2015 to collaborate on those surveys
and, to the extent possible, submit a
single application seeking authorization
for incidental harassment of marine
mammals.
In a similar comment, the NRDC
expressed concern over the number of
activities proposed in the same area for
the same season referencing
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applications for: Furie, Bluecrest,
Buccaneer, and Apache.
Response: We agree and have
encouraged SAE to cooperate with other
interested parties to minimize the
impacts of new seismic surveys in the
region. Apache has told NMFS that their
proposed activities are a separate project
to that of SAE. Currently, SAE works
with other oil and gas operators in the
area to enter into cooperative
agreements. Sometimes these
negotiations are successful, but at other
times the companies cannot reach an
agreement acceptable to both parties.
SAE will continue its discussions with
other operators in Cook Inlet to find
opportunities to joint venture in oil and
gas operations, including seismic data
acquisition.
The portion of the statute cited by the
MMC refers to the need to require
mitigation measures to ensure that the
specified activity for which take is
authorized in that particular
authorization ‘‘effects the least
practicable impact.’’ SAE proposed and
NMFS has required a rigorous
mitigation and monitoring plan to
ensure that SAE’s program meets that
standard. Moreover, NMFS will not
issue IHAs to other applicants if the
negligible impact standard cannot be
met.
Lastly, there are no applications being
processed for Furie or Buccaneer.
Apache does not anticipate conducting
seismic activity in the 2015 season.
Additionally, the activities proposed by
Bluecrest are not seismic surveys and in
a far southerly portion of the Inlet, with
no overlap with SAE’s activities.
Comment 12: Both the NRDC and the
MMC comment that authorization
should not be issued until the Cook
Inlet Beluga Whale Take Recovery Plan
is finalized and published.
Response: The Cook Inlet Beluga
Whale Recovery Plan is still under
development and will not be available
in time to authorize activities for the
2015 open water season. It is possible
the Recovery Plan will be available for
next season. It is not necessary to have
the Recovery Plan finalized to authorize
SAE’s activity, as NMFS is still able to
make a negligible impact determination
for beluga whales.
Comment 13: The MMC comments
that various applicants in the Cook Inlet
region have used differing density
estimates for calculating take of marine
mammal species in the Inlet and that all
applicants should use the same
densities.
Response: The density estimates used
by SAE specifically for harbor
porpoises, harbor seals, and killer
whales are the best available science at
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this time. The data are from NMFS
aerial surveys over a ten year period
(2000–2012). NMFS is working with
applicants to incorporate these density
estimates into future applications and
take authorizations. However, where
applicable, density estimates and
derived take estimation may vary based
on site-specific knowledge of
abundance, density, seasonality, or
other qualities that could allow for a
more nuanced assessment of the
presence of a particular stock in a given
location.
Comment 14: The MMC also
comments that in the application, SAE
states it will only survey in an area of
777km2 but that the proposed action
area is much larger. The MMC requests
that SAE specify the area in which they
expect to operate so that take
estimations more accurately reflect the
scope of the project.
Response: Due to the nature of SAE’s
work, contracts are awarded throughout
the season and the exact locations of
operation are not known to SAE at the
time of the application. However, SAE
has provided how much area they plan
to survey and NMFS has calculated take
estimation using the number of survey
days requested and daily ensonified
area to calculate take instead of the
777km2 unique area specified in the
application to ensure a robust
calculation of exposures to the 160dB
level.
Comment 15: The MMC comments
that SAE should be required to
investigate and report on detection
probabilities from various observation
platforms for differing sea states and
light conditions.
Response: NMFS acknowledges that
collecting detection probabilities from
various platforms under different
conditions would be very useful
information and could better inform
monitoring reports by discerning how
many animals were likely taken.
However, constructing a study to
investigate detection probabilities
requires a great deal of planning and
many more observers than are involved
in this survey. NMFS would like to
work with the MMC in the future to
discuss how best to conduct this work
and refine detection probabilities for
seismic surveys.
Comment 16: The NRDC comments
on several issues under NEPA, related to
cumulative effects and the suite of
alternatives. These comments are: (1)
NEPA mandates that NMFS may not
authorize activities while a
programmatic EIS is underway; (2) The
No Action alternative must assume SAE
will not conduct the proposed activity;
and (3) The third alternative with
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additional mitigation measures is not
sufficiently analyzed and defined.
Response: The NEPA analysis is an
important component of our process.
Our responses to the issues raised by the
NRDC are as follows:
(1) The regulatory text referenced by
NRDC in their comments, 40 CFR
1506.1, states that ‘‘While work on a
required program environmental impact
statement is in progress and the action
is not covered by an existing program
statement, agencies shall not undertake
in the interim any major Federal action
covered by the program which may
significantly affect the quality of the
human environment.’’ NRDC is likely
referencing NMFS’ Federal Register
Notice of Intent to Prepare an EIS for
Cook Inlet (79 FR 61616; October 14,
2014). That provision is not applicable
here as NMFS’ decision to prepare an
EIS is not required, but rather voluntary.
The programmatic EIS is meant to
address hypothetical increasing future
levels of activity in Cook Inlet, not a
specific proposed project. Lastly, the
regulatory text references activities that
are expected to have a significant
impact on the human environment, and
NMFS has determined that this activity
will not have such an impact, as
specified in the Finding of No
Significant Impact (FONSI). At this
time, NMFS is evaluating each activity
individually, taking into consideration
cumulative impacts, with an EA, to
determine if the action under
consideration can support a FONSI.
(2) The No Action alternative in
NMFS’ draft EA for this activity was
written to reflect a situation in which
NMFS did not authorize the activity and
the survey went forward without
mitigation and monitoring. However,
after further consideration, NMFS has
decided to modify the No Action
alternative to represent a situation in
which NMFS did not issue an
authorization and the applicant did not
conduct their proposed activity. These
changes are reflected in the Final EA.
(3) The third alternative in the EA is
a scenario that includes all of the
mitigation measures of the preferred
alternative, as well as additional cutting
edge technologies that have been
suggested by commenters in previous
authorizations, including NRDC.
However, this alternative does not
contain the more detailed analysis
requested by NRDC because many of the
included technologies are not viable at
this time. Many are still in the
developmental or preliminary testing
phase, or do not currently have
guidelines pertaining to appropriate
operating conditions around marine
mammals, such as unmanned aerial
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vehicles. The No Action alternative and
the Preferred alternative both contain
more in-depth analyses as appropriate.
Comment 17: The NRDC comments
that the dates in the proposed IHA
suggest a curtailing of public review in
violation of the Administrative
Procedure Act.
Response: The date provided in the
proposed IHA was the date proposed by
the applicant originally for this work.
Due to the time required to analyze and
respond to comments sufficiently, this
date was postponed and the
authorization will be effective on: May
13, 2015.
Comment 18: The MMC comments
that the use of a 2.5 turnover factor in
take estimation of harbor seals is
inappropriate. The MMC requests that
NMFS use the same density × daily
ensonified area × number of days
formula used for the other species. The
MMC also notes that if NMFS uses a
turnover factor that it should consult the
literature to create a more biologically
relevant turnover factor than Wood et
al. 2012.
Response: After reviewing the
Commission’s comment, NMFS decided
to adjust the method used to estimate
take for harbor seals in Cook Inlet. The
daily ensonified area × number of
survey days × density method yields an
estimate of instances of take that is
19,315. Not only is this likely an
overestimate of instances, but it is also
significantly higher than the number of
individual harbor seals expected to be
exposed, as described in more details in
the Estimated Take section. NMFS
applied the survey method used by
SAE, patch shooting, and applied the
number of days required to shoot a
patch to estimate the number of days an
animal at a given haulout could be
exposed. This is an average of 3 days,
but no more than 5. When this factor is
applied to the overestimate of exposures
by using the ensonified daily area
method, the number of exposed seals is
much lower, at 6,438. This number may
be reduced even further as individuals
could be exposed at multiple patches.
Separately, NMFS then considered the
harbor seal densities alongside
monitoring reports from Apache’s work
in 2012. NMFS looked at the monitoring
reports from Apache’s aerial surveys in
June and used correction factors from
the literature to determine the number
of seals in the water. This number was
also multiplied to match the number of
SAE’s proposed survey days (160) to
yield a number of 8,250 instances of
take, notably lower than 19,315.
Additionally, in their 147 days of
surveying, Apache reported sightings of
285 seals. While it is understood that
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this is lower than the actual number of
exposures, as all seals in the 160dB
range are not visible, this number is 131
times smaller than the calculated
number of exposures using the daily
ensonified area method. These methods
are discussed in greater detail in the
Takes Estimation section of this
document, but in summary we
concluded that not more than 25% of
the population of harbor seals would be
taken.
Description of Marine Mammals in the
Area of the Specified Activity
Marine mammals most likely to be
found in the upper Cook activity area
are the beluga whale (Delphinapterus
leucas), harbor porpoise (Phocoena
phocoena), and harbor seal (Phoca
vitulina). However, these species are
found there in low numbers, and
generally only during the summer fish
runs (Nemeth et al. 2007, Boveng et al.
2012). These species are also found in
the Lower Cook Inlet survey area along
with humpback whales (Megaptera
novaeangliae), minke whales
(Balaenoptera acutorostra), gray whales
(Eschrichtius robustus), killer whales
(Orcinus orca), Dall’s porpoise
(Phocoenoides dalli), and Steller sea
lions (Eumetopia jubatus). Minke
whales have been considered migratory
in Alaska (Allen and Angliss, 2014) but
have recently been observed off Cape
Starichkof and Anchor Point year-round
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(Owl Ridge, 2014). Humpback and gray
whales are seasonal in Lower Cook,
while the remaining species could be
encountered at any time of the year.
During marine mammal monitoring
conducted off Cape Starichkof between
May and August 2013, observers
recorded small numbers of humpback
whales, minke whales, gray whales,
killer whales, and Steller sea lions, and
moderate numbers of harbor porpoises
and harbor seals (Owl Ridge, 2014). This
survey also recorded a single beluga
observed 6 kilometers north of Cape
Starichkof in August 2013. The stock
sizes for marine mammals found in the
project area in Cook Inlet are shown in
Table 1.
TABLE 1—MARINE MAMMALS INHABITING THE COOK INLET ACTION AREA
ESA/MMPA
status 1;
Strategic
(Y/N)
Stock abundance (CV, Nmin, most
recent abundance survey) 2
Relative occurrence in Cook Inlet;
season of occurrence
E/D;Y ............
7,469 (0.095; 5,833; 2000) .....................
-;N ................
1,233 (0.034; N/A; 2003) ........................
-;N ................
19,126 (0.071; 18,017; 2007) .................
Killer whale .............
Eastern North Pacific.
Alaska Resident .....
Occasionally seen in Lower Inlet, summer.
Infrequently occur but reported yearround.
Rare migratory visitor; late winter.
-;N ................
2,347 (N/A; 2,084; 2009) ........................
Beluga whale ..........
Alaska Transient ....
Cook Inlet ...............
-:N ................
E/D;Y ............
345 (N/A; 303; 2003).
312 (0.10; 280; 2012) .............................
Harbor porpoise ......
Gulf of Alaska ........
-;Y ................
31,046 (0.214; 25,987; 1998) .................
Dall’s porpoise ........
Steller sea lion ........
Harbor seal .............
Alaska ....................
Western DPS .........
Cook Inlet/Shelikof
......................
E/D;Y ............
-;N ................
.................................................................
79,300 (N/A; 45,659; 2012) ....................
22,900 (0.053; 21,896; 2006) .................
Species
Stock
Humpback whale ....
Central North Pacific.
Alaska ....................
Minke whale ...........
Gray whale .............
Occasionally sighted in Lowe Cook
Inlet.
Use upper Inlet in summer and lower in
winter: annual.
Widespread in the Inlet: annual (less in
winter).
Infrequently found in Lower Inlet.
Primarily found in lower Inlet.
Frequently found in upper and lower
inlet; annual (more in northern Inlet in
summer).
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Source: Allen and Angliss (20142, 2013), Carretta et al. (2013), Zerbini et al. (2006)
Humpback Whale (Megaptera
novaeangliae)
Although there is considerable
distributional overlap in the humpback
whale stocks that use Alaska, the whales
seasonally found in lower Cook Inlet are
probably of the Central North Pacific
stock. Listed as endangered under the
Endangered Species Act (ESA), this
stock has recently been estimated at
7,469, with the portion of the stock that
feeds in the Gulf of Alaska estimated at
2,845 animals (Allen and Angliss 2014).
The Central North Pacific stock winters
in Hawaii and summers from British
Columbia to the Aleutian Islands
(Calambokidis et al. 1997), including
Cook Inlet.
Humpback use of Cook Inlet is largely
confined to lower Cook Inlet. They have
been regularly seen near Kachemak Bay
during the summer months (Rugh et al.
2005a), and there is a whale-watching
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venture in Homer capitalizing on this
seasonal event. There are anecdotal
observations of humpback whales as far
north as Anchor Point, with recent
summer observations extending to Cape
Starichkof (Owl Ridge 2014).
Humpbacks might be encountered in the
vicinity of Anchor Point if seismic
operations were to occur off the point
during the summer. However, SAE
plans, for the most part, to limit seismic
activity along the Kenai Peninsula to
during the spring and fall.
Minke Whale (Balaenoptera acutorostra)
Minke whales are the smallest of the
rorqual group of baleen whales reaching
lengths of up to 35 feet. They are also
the most common of the baleen whales,
although there are no population
estimates for the North Pacific, although
estimates have been made for some
portions of Alaska. Zerbini et al. (2006)
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estimated the coastal population
between Kenai Fjords and the Aleutian
Islands at 1,233 animals.
During Cook Inlet-wide aerial surveys
conducted from 1993 to 2004, minke
whales were encountered only twice
(1998, 1999), both times off Anchor
Point 16 miles northwest of Homer. A
minke whale was also reported off Cape
Starichkof in 2011 (A. Holmes, pers.
comm.) and 2013 (E. Fernandez and C.
Hesselbach, pers. comm.), suggesting
this location is regularly used by minke
whales, including during the winter.
Recently, several minke whales were
recorded off Cape Starichkof in early
summer 2013 during exploratory
drilling conducted there (Owl Ridge
2014). There are no records north of
Cape Starichkof, and this species is
unlikely to be seen in upper Cook Inlet.
There is a chance of encountering this
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whale during seismic operations along
the Kenai Peninsula in lower Cook Inlet.
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Gray Whale (Eschrichtius robustus)
Each spring, the Eastern North Pacific
stock of gray whale migrates 8,000
kilometers (5,000 miles) northward from
breeding lagoons in Baja California to
feeding grounds in the Bering and
Chukchi seas, reversing their travel
again in the fall (Rice and Wolman
1971). Their migration route is for the
most part coastal until they reach the
feeding grounds. A small portion of
whales do not annually complete the
full circuit, as small numbers can be
found in the summer feeding along the
Oregon, Washington, British Columbia,
and Alaskan coasts (Rice et al. 1984,
Moore et al. 2007).
Human exploitation reduced this
stock to an estimated ‘‘few thousand’’
animals (Jones and Schwartz 2002).
However, by the late 1980s, the stock
was appearing to reach carrying
capacity and estimated to be at 26,600
animals (Jones and Schwartz 2002). By
2002, that stock had been reduced to
about 16,000 animals, especially
following unusually high mortality
events in 1999 and 2000 (Allen and
Angliss 2014). The stock has continued
to grow since then and is currently
estimated at 19,126 animals with a
minimum estimate of 18,017 (Carretta et
al. 2013). Most gray whales migrate past
the mouth of Cook Inlet to and from
northern feeding grounds. However,
small numbers of summering gray
whales have been noted by fisherman
near Kachemak Bay and north of
Anchor Point. Further, summering gray
whales were seen offshore of Cape
Starichkof by marine mammal observers
monitoring Buccaneer’s Cosmopolitan
drilling program in 2013 (Owl Ridge
2014). Regardless, gray whales are not
expected to be encountered in upper
Cook Inlet, where there are no records,
but might be encountered during
seismic operations along the Kenai
Peninsula south of Ninilchik. However,
seismic surveys are not planned in this
region during the summer months when
gray whales are most expected.
Beluga Whale (Delphinapterus leucas)
The Cook Inlet beluga whale Distinct
Population Segment (DPS) is a small
geographically isolated population that
is separated from other beluga
populations by the Alaska Peninsula.
The population is genetically (mtDNA)
distinct from other Alaska populations
suggesting the Peninsula is an effective
barrier to genetic exchange (O’CorryCrowe et al. 1997) and that these whales
may have been separated from other
stocks at least since the last ice age.
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Laidre et al. (2000) examined data from
more than 20 marine mammal surveys
conducted in the northern Gulf of
Alaska and found that sightings of
belugas outside Cook Inlet were
exceedingly rare, and these were
composed of a few stragglers from the
Cook Inlet DPS observed at Kodiak
Island, Prince William Sound, and
Yakutat Bay. Several marine mammal
surveys specific to Cook Inlet (Laidre et
al. 2000, Speckman and Piatt 2000),
including those that concentrated on
beluga whales (Rugh et al. 2000, 2005a),
clearly indicate that this stock largely
confines itself to Cook Inlet. There is no
indication that these whales make
forays into the Bering Sea where they
might intermix with other Alaskan
stocks.
The Cook Inlet beluga DPS was
originally estimated at 1,300 whales in
1979 (Calkins 1989) and has been the
focus of management concerns since
experiencing a dramatic decline in the
1990s. Between 1994 and 1998 the stock
declined 47 percent which was
attributed to overharvesting by
subsistence hunting. Subsistence
hunting was estimated to annually
remove 10 to 15 percent of the
population during this period. Only five
belugas have been harvested since 1999,
yet the population has continued to
decline, with the most recent estimate at
only 312 animals (Allen and Angliss
2014). NMFS listed the population as
‘‘depleted’’ in 2000 as a consequence of
the decline, and as ‘‘endangered’’ under
the Endangered Species Act (ESA) in
2008 when the population failed to
recover following a moratorium on
subsistence harvest. In April 2011,
NMFS designated critical habitat for the
beluga under the ESA (Figure 3). The
most recent aerial survey, conducted in
2014, suggests that the Cook Inlet
population of belugas is comprised of
340 individuals (Shelden et al, 2015).
Prior to the decline, this DPS was
believed to range throughout Cook Inlet
and occasionally into Prince William
Sound and Yakutat (Nemeth et al.
2007). However the range has contracted
coincident with the population
reduction (Speckman and Piatt 2000).
During the summer and fall beluga
whales are concentrated near the
Susitna River mouth, Knik Arm,
Turnagain Arm, and Chickaloon Bay
(Nemeth et al. 2007) where they feed on
migrating eulachon (Thaleichthys paciÉ
cus) and salmon (Onchorhyncus spp.)
(Moore et al. 2000). Critical Habitat Area
1 reflects this summer distribution
(Figure 5 in SAE Application). During
the winter, beluga whales concentrate in
deeper waters in the mid-inlet to Kalgin
Island, and in the shallow waters along
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the west shore of Cook Inlet to
Kamishak Bay (Critical Habitat Area 2;
Figure 5 in SAE Application). Some
whales may also winter in and near
Kachemak Bay.
Harbor Porpoise (Phocoena phocoena)
Harbor porpoise are small (1.5 meters
length), relatively inconspicuous
toothed whales. The Gulf of Alaska
Stock is distributed from Cape Suckling
to Unimak Pass and was most recently
estimated at 31,046 animals (Allen and
Angliss 2014). They are found primarily
in coastal waters less than 100 meters
(100 meters) deep (Hobbs and Waite
2010) where they feed on Pacific herring
(Clupea pallasii), other schooling fishes,
and cephalopods.
Although they have been frequently
observed during aerial surveys in Cook
Inlet, most sightings are of single
animals, and are concentrated at
Chinitna and Tuxedni bays on the west
side of lower Cook Inlet (Rugh et al.
2005a). Dahlheim et al. (2000) estimated
the 1991 Cook Inlet-wide population at
only 136 animals. However, they are
one of the three marine mammals
(besides belugas and harbor seals)
regularly seen in upper Cook Inlet
(Nemeth et al. 2007), especially during
spring eulachon and summer salmon
runs. Because harbor porpoise have
been observed throughout Cook Inlet
during the summer months, including
mid-inlet waters, they could be
encountered during seismic operations
in upper Cook Inlet.
Dall’s Porpoise (Phocoenoides dalli)
Dall’s porpoise are widely distributed
throughout the North Pacific Ocean
including Alaska, although they are not
found in upper Cook Inlet and the
shallower waters of the Bering, Chukchi,
and Beaufort Seas (Allen and Angliss
2014). Compared to harbor porpoise,
Dall’s porpoise prefer the deep offshore
and shelf slope waters. The Alaskan
population has been estimated at 83,400
animals (Allen and Angliss 2014),
making it one of the more common
cetaceans in the state. Dall’s porpoise
have been observed in lower Cook Inlet,
including Kachemak Bay and near
Anchor Point (Owl Ridge 2014), but
sightings there are rare. There is a
remote chance that Dall’s porpoise
might be encountered during seismic
operations along the Kenai Peninsula.
Killer Whale (Orcinus orca)
Two different stocks of killer whales
inhabit the Cook Inlet region of Alaska:
The Alaska Resident Stock and the Gulf
of Alaska, Aleutian Islands, Bering Sea
Transient Stock (Allen and Angliss
2014). The resident stock is estimated at
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2,347 animals and occurs from
Southeast Alaska to the Bering Sea
(Allen and Angliss 2014). Resident
whales feed exclusively on fish and are
genetically distinct from transient
whales (Saulitis et al. 2000). The
transient whales feed primarily on
marine mammals (Saulitis et al. 2000).
The transient population inhabiting the
Gulf of Alaska shares mitochondrial
DNA haplotypes with whales found
along the Aleutian Islands and the
Bering Sea suggesting a common stock,
although there appears to be some
subpopulation genetic structuring
occurring to suggest the gene flow
between groups is limited (see Allen
and Angliss 2014). For the three regions
combined, the transient population has
been estimated at 587 animals (Allen
and Angliss 2014).
Killer whales are occasionally
observed in lower Cook Inlet, especially
near Homer and Port Graham (Shelden
et al. 2003, Rugh et al. 2005a). A
concentration of sightings near Homer
and inside Kachemak Bay may represent
high use or may reflect high observereffort, given most records are from a
whale-watching venture based in
Homer. The few whales that have been
photographically identified in lower
Cook Inlet belong to resident groups
more commonly found in nearby Kenai
Fjords and Prince William Sound
(Shelden et al. 2003). Prior to the 1980s,
killer whale sightings in upper Cook
Inlet were very rare. During aerial
surveys conducted between 1993 and
2004, killer whales were observed on
only three flights, all in the Kachemak
and English Bay area (Rugh et al.
2005a). However, anecdotal reports of
killer whales feeding on belugas in
upper Cook Inlet began increasing in the
1990s, possibly in response to declines
in sea lion and harbor seal prey
elsewhere (Shelden et al. 2003). These
sporadic ventures of transient whales
into beluga summering grounds have
been implicated as a possible
contributor to decline of Cook Inlet
belugas in the 1990s, although the
number of confirmed mortalities from
killer whales is small (Shelden et al.
2003). If killer whales were to venture
into upper Cook Inlet in 2015, they
might be encountered during both
seismic operations in both upper and
lower Cook Inlet.
Steller Sea Lion (Eumetopia jubatus)
The Western Stock of the Steller sea
lion is defined as all populations west
of longitude 144 °W. to the western end
of the Aleutian Islands. The most recent
estimate for this stock is 45,649 animals
(Allen and Angliss 2014), considerably
less than that estimated 140,000 animals
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in the 1950s (Merrick et al. 1987).
Because of this dramatic decline, the
stock was listed under the ESA as a
threatened DPS in 1990, and relisted as
endangered in 1997. Critical habitat was
designated in 1993, and is defined as a
20-nautical-mile radius around all major
rookeries and haulout sites. The 20nautical-mile buffer was established
based on telemetry data that indicated
these sea lions concentrated their
summer foraging effort within this
distance of rookeries and haul outs.
Steller sea lions inhabit lower Cook
Inlet, especially in the vicinity of Shaw
Island and Elizabeth Island (Nagahut
Rocks) haulout sites (Rugh et al. 2005a),
but are rarely seen in upper Cook Inlet
(Nemeth et al. 2007). Of the 42 Steller
sea lion groups recorded during Cook
Inlet aerial surveys between 1993 and
2004, none were recorded north of
Anchor Point and only one in the
vicinity of Kachemak Bay (Rugh et al.
2005a). Marine mammal observers
associated with Buccaneer’s drilling
project off Cape Starichkof did observe
seven Steller sea lions during the
summer of 2013 (Owl Ridge 2014).
The upper reaches of Cook Inlet may
not provide adequate foraging
conditions for sea lions for establishing
a major haul out presence. Steller sea
lions feed largely on walleye pollock
(Theragra chalcogramma), salmon
(Onchorhyncus spp.), and arrowtooth
flounder (Atheresthes stomias) during
the summer, and walleye pollock and
Pacific cod (Gadus macrocephalus)
during the winter (Sinclair and
Zeppelin 2002), none of which, except
for salmon, are found in abundance in
upper Cook Inlet (Nemeth et al. 2007).
Steller sea lions are unlikely to be
encountered during seismic operations
in upper Cook Inlet, but they could
possibly be encountered along the Kenai
Peninsula, especially closer to Anchor
Point.
Harbor Seal (Phoca vitulina)
With more than 150,000 animals
state-wide (Allen and Angliss 2014),
harbor seals are one of the more
common marine mammal species in
Alaskan waters. They are most
commonly seen hauled out at tidal flats
and rocky areas. Harbor seals feed
largely on schooling fish such a walleye
pollock, Pacific cod, salmon, Pacific
herring, eulachon, and squid. Although
harbor seals may make seasonal
movements in response to prey, they are
resident to Alaska and do not migrate.
The Cook Inlet/Shelikof Stock,
ranging from approximately Anchorage
down along the south side of the Alaska
Peninsula to Unimak Pass, has been
recently estimated at a stable 22,900
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(Allen and Angliss 2014). Large
numbers concentrate at the river mouths
and embayments of lower Cook Inlet,
including the Fox River mouth in
Kachemak Bay (Rugh et al. 2005a).
Montgomery et al. (2007) recorded over
200 haulout sites in lower Cook Inlet
alone. However, only a few dozens to a
couple hundred seals seasonally occur
in upper Cook Inlet (Rugh et al. 2005a),
mostly at the mouth of the Susitna River
where their numbers vary in concert
with the spring eulachon and summer
salmon runs (Nemeth et al. 2007,
Boveng et al. 2012). In 2012, up to 100
harbor seals were observed hauled out
at the mouths of the Theodore and
Lewis rivers during monitoring activity
associated with SAE’s (with Apache)
2012 Cook Inlet seismic program.
Montgomery et al. (2007) also found
seals elsewhere in Cook Inlet to move in
response to local steelhead
(Onchorhynchus mykiss) and salmon
runs. Harbor seals may be encountered
during seismic operations in both upper
and lower Cook Inlet.
Potential Effects of the Specified
Activity on Marine Mammals
This section includes a summary and
discussion of the ways that components
(e.g., seismic airgun operations, vessel
movement) of the specified activity,
including mitigation, may impact
marine mammals. The ‘‘Estimated Take
by Incidental Harassment’’ section later
in this document will include a
quantitative analysis of the number of
individuals that are expected to be taken
by this activity. The ‘‘Negligible Impact
Analysis’’ section will include the
analysis of how this specific activity
will impact marine mammals and will
consider the content of this section, the
‘‘Estimated Take by Incidental
Harassment’’ section, the ‘‘Mitigation’’
section, and the ‘‘Anticipated Effects on
Marine Mammal Habitat’’ section to
draw conclusions regarding the likely
impacts of this activity on the
reproductive success or survivorship of
individuals and from that on the
affected marine mammal populations or
stocks.
Operating active acoustic sources,
such as airgun arrays, has the potential
for adverse effects on marine mammals.
The majority of anticipated impacts will
be from the use of acoustic sources.
Acoustic Impacts
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 have been
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derived using auditory evoked
potentials, anatomical modeling, and
other data. Southall et al. (2007)
designated ‘‘functional hearing groups’’
for marine mammals and estimate the
lower and upper frequencies of
functional hearing of the groups. The
functional groups and the associated
frequencies are indicated below (note
that animals are less sensitive to sounds
at the outer edge of their functional
range and most sensitive to sounds of
frequencies within a smaller range
somewhere in the middle of their
functional hearing range) and have been
modified slightly from Southall et al.
2007 to incorporate some newer
information:
• Low frequency cetaceans (13
species of mysticetes): functional
hearing is estimated to occur between
approximately 7 Hz and 30 kHz; (Ketten
and Mountain 2009; Tubelli et al. 2012)
• 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; (Southall et al. 2007)
• 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; (Southall et al 2007)
• Phocid pinnipeds in Water:
Functional hearing is estimated to occur
between approximately 75 Hz and 100
¨
kHz; (Hemila et al. 2006; Mulsow et al.
2011; Reichmuth et al. 2013) and
• Otariid pinnipeds in Water:
Functional hearing is estimated to occur
between approximately 100 Hz and 40
kHz. (Reichmuth et al. 2013)
As mentioned previously in this
document, nine marine mammal species
(seven cetacean and two pinniped
species) are likely to occur in the
seismic survey area. Of the seven
cetacean species likely to occur in SAE’s
project area, three classified as a lowfrequency cetaceans (humpback, minke,
gray whale), two are classified as midfrequency cetaceans (beluga and killer
whales), and two are classified as a
high-frequency cetaceans (Dall’s and
harbor porpoise) (Southall et al., 2007).
Of the two pinniped species likely to
occur in SAE’s project area, one is
classified as a phocid (harbor seal), and
one is classified as an otariid (Steller sea
lion). A species’ functional hearing
group is a consideration when we
analyze the effects of exposure to sound
on marine mammals.
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1. Potential Effects of Airgun Sounds on
Marine Mammals
The effects of sounds from airgun
pulses might include one or more of the
following: Tolerance, masking of natural
sounds, behavioral disturbance, and
temporary or permanent hearing
impairment or non-auditory effects
(Richardson et al., 1995). As outlined in
previous NMFS documents, the effects
of noise on marine mammals are highly
variable, often depending on species
and contextual factors (based on
Richardson et al., 1995).
Tolerance: Numerous studies have
shown that pulsed sounds from air guns
are often readily detectable in the water
at distances of many kilometers.
Numerous studies have also shown that
marine mammals at distances more than
a few kilometers from operating survey
vessels often show no apparent
response. That is often true even in
cases when the pulsed sounds must be
readily audible to the animals based on
measured received levels and the
hearing sensitivity of that mammal
group. In general, pinnipeds and small
odontocetes (toothed whales) seem to be
more tolerant of exposure to air gun
pulses than baleen whales. Although
various toothed whales, and (less
frequently) pinnipeds have been shown
to react behaviorally to airgun pulses
under some conditions, at other times,
mammals of both types have shown no
overt reactions. Weir (2008) observed
marine mammal responses to seismic
pulses from a 24 airgun array firing a
total volume of either 5,085 in3 or 3,147
in3 in Angolan waters between August
2004 and May 2005. Weir recorded a
total of 207 sightings of humpback
whales (n = 66), sperm whales (n = 124),
and Atlantic spotted dolphins (n = 17)
and reported that there were no
significant differences in encounter
rates (sightings/hr) for humpback and
sperm whales according to the airgun
array’s operational status (i.e., active
versus silent).
Behavioral Disturbance: Marine
mammals may behaviorally respond
when exposed to anthropogenic noise.
These behavioral reactions are often
shown as: Changing durations of
surfacing and dives, number of blows
per surfacing, or moving direction and/
or speed; reduced/increased vocal
activities; changing/cessation of certain
behavioral activities (such as socializing
or feeding); visible startle response or
aggressive behavior (such as tail/fluke
slapping or jaw clapping); avoidance of
areas where noise sources are located;
and/or flight responses (e.g., pinnipeds
flushing into water from haulouts or
rookeries).
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The biological significance of many of
these behavioral disturbances is difficult
to predict. The consequences of
behavioral modification to individual
fitness can range from none up to
potential changes to growth, survival, or
reproduction, depending on the context,
duration, and degree of behavioral
modification. Examples of behavioral
modifications that could impact growth,
survival or reproduction include:
Drastic changes in diving/surfacing/
swimming patterns that lead to
stranding (such as those associated with
beaked whale strandings related to
exposure to military mid-frequency
tactical sonar); longer-term
abandonment of habitat that is
specifically important for feeding,
reproduction, or other critical needs, or
significant disruption of feeding or
social interaction resulting in
substantive energetic costs, inhibited
breeding, or prolonged or permanent
cow-calf separation.
The onset of behavioral disturbance
from anthropogenic noise depends on
both external factors (characteristics of
noise sources and their paths) and the
receiving animals (hearing, motivation,
experience, demography) and is also
difficult to predict (Southall et al.,
2007).
Toothed whales. Few systematic data
are available describing reactions of
toothed whales to noise pulses.
However, systematic work on sperm
whales (Tyack et al., 2003) has yielded
an increasing amount of information
about responses of various odontocetes
to seismic surveys based on monitoring
studies (e.g., Stone, 2003; Smultea et al.,
2004; Moulton and Miller, 2005). Stone
et al., 2003 reported reduced sighting
rates of small odontoceter during
periods of shooting during seismic
surveys with large airgun arryas.
Moulton and Miller (2004) also found
that the range of audibility of seismic
pules for mid-sized odontecetes was
largely underestimated by models.
Seismic operators and marine
mammal observers sometimes see
dolphins and other small toothed
whales near operating airgun arrays,
but, in general, there seems to be a
tendency for most delphinids to show
some limited avoidance of seismic
vessels operating large airgun systems.
However, some dolphins seem to be
attracted to the seismic vessel and
floats, and some ride the bow wave of
the seismic vessel even when large
arrays of airguns are firing. Nonetheless,
there have been indications that small
toothed whales sometimes move away
or maintain a somewhat greater distance
from the vessel when a large array of
airguns is operating than when it is
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silent (e.g., Goold, 1996a,b,c;
Calambokidis and Osmek, 1998; Stone,
2003). The beluga may be a species that
(at least in certain geographic areas)
shows long-distance avoidance of
seismic vessels. Aerial surveys during
seismic operations in the southeastern
Beaufort Sea recorded much lower
sighting rates of beluga whales within
10–20 km (6.2–12.4 mi) of an active
seismic vessel. These results were
consistent with the low number of
beluga sightings reported by observers
aboard the seismic vessel, suggesting
that some belugas might have been
avoiding the seismic operations at
distances of 10–20 km (6.2–12.4 mi)
(Miller et al., 2005).
Captive bottlenose dolphins and (of
more relevance in this project) beluga
whales exhibit changes in behavior
when exposed to strong pulsed sounds
similar in duration to those typically
used in seismic surveys (Finneran et al.,
2002, 2005). However, the animals
tolerated high received levels of sound
(pk–pk level >200 dB re 1 mPa) before
exhibiting aversive behaviors.
Observers stationed on seismic
vessels operating off the United
Kingdom from 1997–2000 have
provided data on the occurrence and
behavior of various toothed whales
exposed to seismic pulses (Stone, 2003;
Gordon et al., 2004). Killer whales were
found to be significantly farther from
large airgun arrays during periods of
shooting compared with periods of no
shooting. The displacement of the
median distance from the array was
approximately 0.5 km (0.3 mi) or more.
Killer whales also appear to be more
tolerant of seismic shooting in deeper
water.
Reactions of toothed whales to large
arrays of airguns are variable and, at
least for delphinids, seem to be confined
to a smaller radius than has been
observed for mysticetes. However, based
on the limited existing evidence,
belugas should not necessarily generally
be grouped with delphinids in the ‘‘less
responsive’’ category.
Pinnipeds. Pinnipeds are not likely to
show a strong avoidance reaction to the
airgun sources used. Visual monitoring
from seismic vessels has shown only
slight (if any) avoidance of airguns by
pinnipeds and only slight (if any)
changes in behavior. Monitoring work
in the Alaskan Beaufort Sea during
1996–2001 provided considerable
information regarding the behavior of
Arctic ice seals exposed to seismic
pulses (Harris et al., 2001; Moulton and
Lawson, 2002). These seismic projects
usually involved arrays of 6 to 16
airguns with total volumes of 560 to
1,500 in3. The combined results suggest
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that some seals avoid the immediate
area around seismic vessels. In most
survey years, ringed seal sightings
tended to be farther away from the
seismic vessel when the airguns were
operating than when they were not
(Moulton and Lawson, 2002). However,
these avoidance movements were
relatively small, on the order of 100 m
(328 ft) to a few hundreds of meters, and
many seals remained within 100–200 m
(328–656 ft) of the trackline as the
operating airgun array passed by. Seal
sighting rates at the water surface were
lower during airgun array operations
than during no-airgun periods in each
survey year except 1997. Similarly, seals
are often very tolerant of pulsed sounds
from seal-scaring devices (Mate and
Harvey, 1987; Jefferson and Curry, 1994;
Richardson et al., 1995a). However,
initial telemetry work suggests that
avoidance and other behavioral
reactions by two other species of seals,
grey and harbor seals, to small airgun
sources may at times be stronger than
evident to date from visual studies of
pinniped reactions to airguns
(Thompson et al., 1998). Even if
reactions of the species occurring in the
activity area are as strong as those
evident in the telemetry study, reactions
are expected to be confined to relatively
small distances and durations, with no
long-term effects on pinniped
individuals or populations.
Masking: Masking is the obscuring of
sounds of interest by other sounds, often
at similar frequencies. Marine mammals
use acoustic signals for a variety of
purposes, which differ among species,
but include communication between
individuals, navigation, foraging,
reproduction, avoiding predators, and
learning about their environment (Erbe
and Farmer, 2000; Tyack, 2000).
Masking, or auditory interference,
generally occurs when sounds in the
environment are louder than, and of a
similar frequency to, auditory signals an
animal is trying to receive. Masking is
a phenomenon that affects animals
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.
Masking occurs when anthropogenic
sounds and signals (that the animal
utilizes) overlap at both spectral and
temporal scales. For the airgun sound
generated from the seismic surveys,
sound will consist of low frequency
(under 500 Hz) pulses with extremely
short durations (less than one second).
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Lower frequency man-made sounds are
more likely to affect detection of
potentially important natural sounds
such as surf and prey noise, or
communication calls for low frequency
specialists. There is little concern
regarding masking near the sound
source due to the brief duration of these
pulses and relatively longer silence
between air gun shots (approximately 12
seconds). However, at long distances
(over tens of kilometers away), due to
multipath propagation and
reverberation, the durations of airgun
pulses can be ‘‘stretched’’ to seconds
with long decays (Madsen et al., 2006),
although the intensity of the sound is
greatly reduced.
This could affect communication
signals used by low frequency
mysticetes when they occur near the
noise band and thus reduce the
communication space of animals (e.g.,
Clark et al., 2009) and cause increased
stress levels (e.g., Foote et al., 2004; Holt
et al., 2009); however, no baleen whales
are expected to occur within the action
area. Marine mammals are thought to be
able to compensate for masking by
adjusting their acoustic behavior by
shifting call frequencies, and/or
increasing call volume and vocalization
rates. For example, blue whales were
found to increase call rates when
exposed to seismic survey noise in the
St. Lawrence Estuary (Di Iorio and
Clark, 2010). The North Atlantic right
whales (Eubalaena glacialis) exposed to
high shipping noise increase call
frequency (Parks et al., 2007), while
some humpback whales respond to lowfrequency active sonar playbacks by
increasing song length (Miller et al.,
2000). Additionally, beluga whales have
been known to change their
vocalizations in the presence of high
background noise possibly to avoid
masking calls (Au et al., 1985; Lesage et
al., 1999; Scheifele et al., 2005).
Although some degree of masking is
inevitable when high levels of manmade
broadband sounds are introduced into
the sea, marine mammals have evolved
systems and behavior that function to
reduce the impacts of masking.
Structured signals, such as the
echolocation click sequences of small
toothed whales, may be readily detected
even in the presence of strong
background noise because their
frequency content and temporal features
usually differ strongly from those of the
background noise (Au and Moore, 1988,
1990). The components of background
noise that are similar in frequency to the
sound signal in question primarily
determine the degree of masking of that
signal.
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Redundancy and context can also
facilitate detection of weak signals.
These phenomena may help marine
mammals detect weak sounds in the
presence of natural or manmade noise.
Most masking studies in marine
mammals present the test signal and the
masking noise from the same direction.
The sound localization abilities of
marine mammals suggest that, if signal
and noise come from different
directions, masking would not be as
severe as the usual types of masking
studies might suggest (Richardson et al.,
1995). The dominant background noise
may be highly directional if it comes
from a particular anthropogenic source
such as a ship or industrial site.
Directional hearing may significantly
reduce the masking effects of these
sounds by improving the effective
signal-to-noise ratio. In the cases of
higher frequency hearing by the
bottlenose dolphin, beluga whale, and
killer whale, empirical evidence
confirms that masking depends strongly
on the relative directions of arrival of
sound signals and the masking noise
(Penner et al., 1986; Dubrovskiy, 1990;
Bain et al., 1993; Bain and Dahlheim,
1994). Toothed whales and probably
other marine mammals as well, have
additional capabilities besides
directional hearing that can facilitate
detection of sounds in the presence of
background noise. There is evidence
that some toothed whales can shift the
dominant frequencies of their
echolocation signals from a frequency
range with a lot of ambient noise toward
frequencies with less noise (Au et al.,
1974, 1985; Moore and Pawloski, 1990;
Thomas and Turl, 1990; Romanenko
and Kitain, 1992; Lesage et al., 1999). A
few marine mammal species are known
to increase the source levels or alter the
frequency of their calls in the presence
of elevated sound levels (Dahlheim,
1987; Au, 1993; Lesage et al., 1993,
1999; Terhune, 1999; Foote et al., 2004;
Parks et al., 2007, 2009; Di Iorio and
Clark, 2009; Holt et al., 2009).
These data demonstrating adaptations
for reduced masking pertain mainly to
the very high frequency echolocation
signals of toothed whales. There is less
information about the existence of
corresponding mechanisms at moderate
or low frequencies or in other types of
marine mammals. For example, Zaitseva
et al. (1980) found that, for the
bottlenose dolphin, the angular
separation between a sound source and
a masking noise source had little effect
on the degree of masking when the
sound frequency was 18 kHz, in contrast
to the pronounced effect at higher
frequencies. Directional hearing has
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been demonstrated at frequencies as low
as 0.5–2 kHz in several marine
mammals, including killer whales
(Richardson et al., 1995a). This ability
may be useful in reducing masking at
these frequencies. In summary, high
levels of sound generated by
anthropogenic activities may act to
mask the detection of weaker
biologically important sounds by some
marine mammals. This masking may be
more prominent for lower frequencies.
For higher frequencies, such as that
used in echolocation by toothed whales,
several mechanisms are available that
may allow them to reduce the effects of
such masking.
Threshold Shift (noise-induced loss of
hearing)—When animals exhibit
reduced hearing sensitivity (i.e., sounds
must be louder for an animal to detect
them) following exposure to an intense
sound or sound for long duration, it is
referred to as a noise-induced threshold
shift (TS). An animal can experience
temporary threshold shift (TTS) or
permanent threshold shift (PTS). TTS
can last from minutes or hours to days
(i.e., there is complete recovery), can
occur in specific frequency ranges (i.e.,
an animal might only have a temporary
loss of hearing sensitivity between the
frequencies of 1 and 10 kHz), and can
be of varying amounts (for example, an
animal’s hearing sensitivity might be
reduced initially by only 6 dB or
reduced by 30 dB). PTS is permanent,
but some recovery is possible. PTS can
also occur in a specific frequency range
and amount as mentioned above for
TTS.
The following physiological
mechanisms are thought to play a role
in inducing auditory TS: Effects to
sensory hair cells in the inner ear that
reduce their sensitivity, modification of
the chemical environment within the
sensory cells, residual muscular activity
in the middle ear, displacement of
certain inner ear membranes, increased
blood flow, and post-stimulatory
reduction in both efferent and sensory
neural output (Southall et al., 2007).
The amplitude, duration, frequency,
temporal pattern, and energy
distribution of sound exposure all can
affect the amount of associated TS and
the frequency range in which it occurs.
As amplitude and duration of sound
exposure increase, so, generally, does
the amount of TS, along with the
recovery time. For intermittent sounds,
less TS could occur than compared to a
continuous exposure with the same
energy (some recovery could occur
between intermittent exposures
depending on the duty cycle between
sounds) (Kryter et al., 1966; Ward,
1997). For example, one short but loud
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(higher SPL) sound exposure may
induce the same impairment as one
longer but softer sound, which in turn
may cause more impairment than a
series of several intermittent softer
sounds with the same total energy
(Ward, 1997). Additionally, though TTS
is temporary, prolonged exposure to
sounds strong enough to elicit TTS, or
shorter-term exposure to sound levels
well above the TTS threshold, can cause
PTS, at least in terrestrial mammals
(Kryter, 1985). In the case of the seismic
survey, 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
papers on hearing impairments that can
occur with exposure to a loud sound,
only a few studies provide empirical
information on the levels at which
noise-induced loss in hearing sensitivity
occurs in nonhuman animals. For
marine mammals, published data are
limited to the captive bottlenose
dolphin, beluga, harbor porpoise, and
Yangtze finless porpoise (Finneran et
al., 2000, 2002, 2003, 2005, 2007, 2010a,
2010b; Finneran and Schlundt, 2010;
Lucke et al., 2009; Mooney et al., 2009a,
2009b; Popov et al., 2011a, 2011b;
Kastelein et al., 2012a; Schlundt et al.,
2000; Nachtigall et al., 2003, 2004). For
pinnipeds in water, data are limited to
measurements of TTS in harbor seals, an
elephant seal, and California sea lions
(Kastak et al., 1999, 2005; Kastelein et
al., 2012b).
Marine mammal hearing plays a
critical role in communication with
conspecifics, and interpretation of
environmental cues for purposes such
as predator avoidance and prey capture.
Depending on the degree (elevation of
threshold in dB), duration (i.e., recovery
time), and frequency range of TTS, and
the context in which it is experienced,
TTS can have effects on marine
mammals ranging from discountable to
serious (similar to those discussed in
auditory masking, below). For example,
a marine mammal may be able to readily
compensate for a brief, relatively small
amount of TTS in a non-critical
frequency range that occurs during a
time where ambient noise is lower and
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there are not as many competing sounds
present. Alternatively, a larger amount
and longer duration of TTS sustained
during time when communication is
critical for successful mother/calf
interactions could have more serious
impacts. Similarly, depending on the
degree and frequency range, the effects
of PTS on an animal could range in
severity, although it is considered
generally more serious because it is a
permanent condition. Of note, reduced
hearing sensitivity as a simple function
of aging has been observed in marine
mammals, as well as humans and other
taxa (Southall et al., 2007), so we can
infer that strategies exist for coping with
this condition to some degree, though
likely not without cost.
Given the higher level of sound
necessary to cause PTS as compared
with TTS, it is considerably less likely
that PTS would occur during the
seismic surveys in Cook Inlet. Cetaceans
generally avoid the immediate area
around operating seismic vessels, as do
some other marine mammals. Some
pinnipeds show avoidance reactions to
airguns, but their avoidance reactions
are generally not as strong or consistent
as those of cetaceans, and occasionally
they seem to be attracted to operating
seismic vessels (NMFS, 2010).
Non-auditory Physical Effects: Nonauditory physical effects might occur in
marine mammals exposed to strong
underwater pulsed sound. Possible
types of non-auditory physiological
effects or injuries that theoretically
might occur in mammals close to a
strong sound source include stress,
neurological effects, bubble formation,
and other types of organ or tissue
damage. Some marine mammal species
(i.e., beaked whales) may be especially
susceptible to injury and/or stranding
when exposed to strong pulsed sounds.
Classic stress responses begin when
an animal’s central nervous system
perceives a potential threat to its
homeostasis. That perception triggers
stress responses regardless of whether a
stimulus actually threatens the animal;
the mere perception of a threat is
sufficient to trigger a stress response
(Moberg, 2000; Sapolsky et al., 2005;
Seyle, 1950). Once an animal’s central
nervous system perceives a threat, it
mounts a biological response or defense
that consists of a combination of the
four general biological defense
responses: Behavioral responses;
autonomic nervous system responses;
neuroendocrine responses; or immune
responses.
In the case of many stressors, an
animal’s first and most economical (in
terms of biotic costs) response is
behavioral avoidance of the potential
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stressor or avoidance of continued
exposure to a stressor. An animal’s
second line of defense to stressors
involves the sympathetic part of the
autonomic nervous system and the
classical ‘‘fight or flight’’ response,
which includes the cardiovascular
system, the gastrointestinal system, the
exocrine glands, and the adrenal
medulla to produce changes in heart
rate, blood pressure, and gastrointestinal
activity that humans commonly
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 neuroendocrine
functions that are affected by stress—
including immune competence,
reproduction, metabolism, and
behavior—are regulated by pituitary
hormones. Stress-induced changes in
the secretion of pituitary hormones have
been implicated in failed reproduction
(Moberg, 1987; Rivier, 1995), altered
metabolism (Elasser et al., 2000),
reduced immune competence (Blecha,
2000), and behavioral disturbance.
Increases in the circulation of
glucocorticosteroids (cortisol,
corticosterone, and aldosterone in
marine mammals; see Romano et al.,
2004) have been equated with stress for
many years.
The primary distinction between
stress (which is adaptive and does not
normally place an animal at risk) and
distress is the biotic cost of the
response. During a stress response, an
animal uses glycogen stores that can be
quickly replenished once the stress is
alleviated. In such circumstances, the
cost of the stress response would not
pose a risk to the animal’s welfare.
However, when an animal does not have
sufficient energy reserves to satisfy the
energetic costs of a stress response,
energy resources must be diverted from
other biotic 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 fitness will
suffer. In these cases, the animals will
have entered a pre-pathological or
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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. Note that these
examples involved a long-term (days or
weeks) stress response due to exposure
to stimuli.
Relationships between these
physiological mechanisms, animal
behavior, and the costs of stress
responses have also been documented
fairly well through controlled
experiment; 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
anthropogenic sound exposure, 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 anthropogenic sounds.
For example, Jansen (1998) reported
on the relationship between acoustic
exposures and physiological responses
that are indicative of stress responses in
humans (e.g., 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 noiseinduced physiological transient stress
responses in hearing-specialist fish (i.e.,
goldfish) that accompanied short- and
long-term hearing losses. Welch and
Welch (1970) reported physiological
and behavioral stress responses that
accompanied damage to the inner ears
of fish and several mammals.
Hearing is one of the primary senses
marine mammals use to gather
information about their environment
and communicate with conspecifics.
Although empirical information on the
effects of sensory impairment (TTS,
PTS, and acoustic masking) on marine
mammals remains limited, we assume
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that reducing a marine mammal’s ability
to gather information about its
environment and communicate with
other members of its species would
induce stress, based on data that
terrestrial animals exhibit those
responses under similar conditions
(NRC, 2003) and because marine
mammals 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. However, marine
mammals also 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), NMFS also
assumes that stress responses could
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. Resonance effects (Gentry, 2002)
and direct noise-induced bubble
formations (Crum et al., 2005) are
implausible in the case of exposure to
an impulsive broadband source like an
airgun array. If seismic surveys disrupt
diving patterns of deep-diving species,
this might result in bubble formation
and a form of the bends, as speculated
to occur in beaked whales exposed to
sonar. However, there is no specific
evidence of this upon exposure to
airgun pulses. Additionally, no beaked
whale species occur in the seismic
survey area.
In general, very little is known about
the potential for strong, anthropogenic
underwater sounds to cause nonauditory physical effects in marine
mammals. Such effects, if they occur at
all, would presumably be limited to
short distances and to activities that
extend over a prolonged period. The
available data do not allow
identification of a specific exposure
level above which non-auditory effects
can be expected (Southall et al., 2007)
or any meaningful quantitative
predictions of the numbers (if any) of
marine mammals that might be affected
in those ways. There is no definitive
evidence that any of these effects occur
even for marine mammals in close
proximity to large arrays of airguns. In
addition, marine mammals that show
behavioral avoidance of seismic vessels,
including belugas and some pinnipeds,
are especially unlikely to incur nonauditory impairment or other physical
effects. Therefore, it is unlikely that
such effects would occur during SAE’s
surveys given the brief duration of
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exposure and the planned monitoring
and mitigation measures described later
in this document.
Stranding and Mortality: Marine
mammals close to underwater
detonations of high explosive can be
killed or severely injured, and the
auditory organs are especially
susceptible to injury (Ketten et al. 1993;
Ketten 1995). Airgun pulses are less
energetic and their peak amplitudes
have slower rise times. To date, there is
no evidence that serious injury, death,
or stranding by marine mammals can
occur from exposure to air gun pulses,
even in the case of large air gun arrays.
However, in past IHA notices for
seismic surveys, commenters have
referenced two stranding events
allegedly associated with seismic
activities, one off Baja California and a
second off Brazil. NMFS has addressed
this concern several times, including in
the Federal Register notice announcing
the IHA for Apache Alaska’s first
seismic survey in 2012. Readers are
encouraged to review NMFS’s response
to comments on this matter found in 69
FR 74905 (December 14, 2004), 71 FR
43112 (July 31, 2006), 71 FR 50027
(August 24, 2006), 71 FR 49418 (August
23, 2006), and 77 FR 27720 (May 11,
2012).
Beluga whale strandings in Cook Inlet
are not uncommon; however, these
events often coincide with extreme tidal
fluctuations (‘‘spring tides’’) or killer
whale sightings (Shelden et al., 2003).
For example, in August 2012, a group of
Cook Inlet beluga whales stranded in
the mud flats of Turnagain Arm during
low tide and were able to swim free
with the flood tide. No strandings or
marine mammals in distress were
observed during the 2D test survey
conducted by Apache in March 2011,
and none were reported by Cook Inlet
inhabitants. As a result, NMFS does not
expect any marine mammals will incur
serious injury or mortality in Cook Inlet
or strand as a result of the seismic
survey.
2. Potential Effects From Pingers on
Marine Mammals
Active acoustic sources other than the
airguns will be used for SAE’s oil and
gas exploration seismic survey program
in Cook Inlet. The specifications for the
pingers (source levels and frequency
ranges) were provided earlier in this
document. In general, pingers are
known to cause behavioral disturbance
and are commonly used to deter marine
mammals from commercial fishing gear
or fish farms. Due to the potential to
change marine mammal behavior, shut
downs described for airguns will also be
applied to pinger use.
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Vessel Impacts
Vessel activity and noise associated
with vessel activity will temporarily
increase in the action area during SAE’s
seismic survey as a result of the
operation of nine vessels. To minimize
the effects of vessels and noise
associated with vessel activity, SAE will
follow NMFS’s Marine Mammal
Viewing Guidelines and Regulations
and will alter heading or speed if a
marine mammal gets too close to a
vessel. In addition, vessels will be
operating at slow speed (4–5 knots)
when conducting surveys and in a
purposeful manner to and from work
sites in as direct a route as possible.
Marine mammal monitoring observers
and passive acoustic devices will alert
vessel captains as animals are detected
to ensure safe and effective measures are
applied to avoid coming into direct
contact with marine mammals.
Therefore, NMFS neither anticipates nor
authorizes takes of marine mammals
from ship strikes.
Odontocetes, such as beluga whales,
killer whales, and harbor porpoises,
often show tolerance to vessel activity;
however, they may react at long
distances if they are confined by ice,
shallow water, or were previously
harassed by vessels (Richardson et al.,
1995). Beluga whale response to vessel
noise varies greatly from tolerance to
extreme sensitivity depending on the
activity of the whale and previous
experience with vessels (Richardson et
al., 1995). Reactions to vessels depend
on whale activities and experience,
habitat, boat type, and boat behavior
(Richardson et al., 1995) and may
include behavioral responses, such as
altered headings or avoidance (Blane
and Jaakson, 1994; Erbe and Farmer,
2000); fast swimming; changes in
vocalizations (Lesage et al., 1999;
Scheifele et al., 2005); and changes in
dive, surfacing, and respiration patterns.
There are few data published on
pinniped responses to vessel activity,
and most of the information is anecdotal
(Richardson et al., 1995). Generally, sea
lions in water show tolerance to close
and frequently approaching vessels and
sometimes show interest in fishing
vessels. They are less tolerant when
hauled out on land; however, they
rarely react unless the vessel approaches
within 100–200 m (330–660 ft; reviewed
in Richardson et al., 1995).
Entanglement
Although some of SAE’s equipment
contains cables or lines, the risk of
entanglement is extremely remote.
Additionally, mortality from
entanglement is not anticipated. The
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etc.), bivalves, squid, octopus, and
gastropods.
material used by SAE and the amount
of slack is not anticipated to allow for
marine mammal entanglements.
tkelley on DSK3SPTVN1PROD with NOTICES2
Anticipated Effects on Marine Mammal
Habitat
The primary potential impacts to
marine mammal habitat and other
marine species are associated with
elevated sound levels produced by
airguns and other active acoustic
sources. However, other potential
impacts to the surrounding habitat from
physical disturbance are also possible.
This section describes the potential
impacts to marine mammal habitat from
the specified activity. Because the
marine mammals in the area feed on
fish and/or invertebrates there is also
information on the species typically
preyed upon by the marine mammals in
the area. As noted earlier, upper Cook
Inlet is an important feeding and calving
area for the Cook Inlet beluga whale and
critical habitat has been designated for
this species in the seismic survey area.
Common Marine Mammal Prey in the
Project Area
Fish are the primary prey species for
marine mammals in upper Cook Inlet.
Beluga whales feed on a variety of fish,
shrimp, squid, and octopus (Burns and
Seaman, 1986). Common prey species in
Knik Arm include salmon, eulachon
and cod. Harbor seals feed on fish such
as pollock, cod, capelin, eulachon,
Pacific herring, and salmon, as well as
a variety of benthic species, including
crabs, shrimp, and cephalopods. Harbor
seals are also opportunistic feeders with
their diet varying with season and
location. The preferred diet of the
harbor seal in the Gulf of Alaska
consists of pollock, octopus, capelin,
eulachon, and Pacific herring (Calkins,
1989). Other prey species include cod,
flat fishes, shrimp, salmon, and squid
(Hoover, 1988). Harbor porpoises feed
primarily on Pacific herring, cod,
whiting (hake), pollock, squid, and
octopus (Leatherwood et al., 1982). In
the upper Cook Inlet area, harbor
porpoise feed on squid and a variety of
small schooling fish, which would
likely include Pacific herring and
eulachon (Bowen and Siniff, 1999;
NMFS, unpublished data). Killer whales
feed on either fish or other marine
mammals depending on genetic type
(resident versus transient respectively).
Killer whales in Knik Arm are typically
the transient type (Shelden et al., 2003)
and feed on beluga whales and other
marine mammals, such as harbor seal
and harbor porpoise. The Steller sea
lion diet consists of a variety of fishes
(capelin, cod, herring, mackerel,
pollock, rockfish, salmon, sand lance,
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Potential Impacts on Prey Species
With regard to fish as a prey source
for cetaceans and pinnipeds, fish are
known to hear and react to sounds and
to use sound to communicate (Tavolga
et al., 1981) and possibly avoid
predators (Wilson and Dill, 2002).
Experiments have shown that fish can
sense both the strength and direction of
sound (Hawkins, 1981). Primary factors
determining whether a fish can sense a
sound signal, and potentially react to it,
are the frequency of the signal and the
strength of the signal in relation to the
natural background sound level.
Fishes produce sounds that are
associated with behaviors that include
territoriality, mate search, courtship,
and aggression. It has also been
speculated that sound production may
provide the means for long distance
communication and communication
under poor underwater visibility
conditions (Zelick et al., 1999), although
the fact that fish communicate at lowfrequency sound levels where the
masking effects of ambient noise are
naturally highest suggests that very long
distance communication would rarely
be possible. Fishes have evolved a
diversity of sound generating organs and
acoustic signals of various temporal and
spectral contents. Fish sounds vary in
structure, depending on the mechanism
used to produce them (Hawkins, 1993).
Generally, fish sounds are
predominantly composed of low
frequencies (less than 3 kHz).
Since objects in the water scatter
sound, fish are able to detect these
objects through monitoring the ambient
noise. Therefore, fish are probably able
to detect prey, predators, conspecifics,
and physical features by listening to
environmental sounds (Hawkins, 1981).
There are two sensory systems that
enable fish to monitor the vibrationbased information of their surroundings.
The two sensory systems, the inner ear
and the lateral line, constitute the
acoustico-lateralis system.
Although the hearing sensitivities of
very few fish species have been studied
to date, it is becoming obvious that the
intra- and inter-specific variability is
considerable (Coombs, 1981). Nedwell
et al. (2004) compiled and published
available fish audiogram information. A
noninvasive electrophysiological
recording method known as auditory
brainstem response is now commonly
used in the production of fish
audiograms (Yan, 2004). Popper and
Carlson (1998) and the Navy (2001)
found that fish generally perceive
underwater sounds in the frequency
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range of 50–2,000 Hz, with peak
sensitivities below 800 Hz. Even though
some fish are able to detect sounds in
the ultrasonic frequency range, the
thresholds at these higher frequencies
tend to be considerably higher than
those at the lower end of the auditory
frequency range.
Fish are sensitive to underwater
impulsive sounds due to swim bladder
resonance. As the pressure wave passes
through a fish, the swim bladder is
rapidly squeezed as the high pressure
wave, and then the under pressure
component of the wave, passes through
the fish. The swim bladder may
repeatedly expand and contract at the
high sound pressure levels, creating
pressure on the internal organs
surrounding the swim bladder.
Literature relating to the impacts of
sound on marine fish species can be
divided into the following categories: (1)
Pathological effects; (2) physiological
effects; and (3) behavioral effects.
Pathological effects include lethal and
sub-lethal physical damage to fish;
physiological effects include primary
and secondary stress responses; and
behavioral effects include changes in
exhibited behaviors of fish. Behavioral
changes might be a direct reaction to a
detected sound or a result of the
anthropogenic sound masking natural
sounds that the fish normally detect and
to which they respond. The three types
of effects are often interrelated in
complex ways. For example, some
physiological and behavioral effects
could potentially lead to the ultimate
pathological effect of mortality. Hastings
and Popper (2005) reviewed what is
known about the effects of sound on
fishes and identified studies needed to
address areas of uncertainty relative to
measurement of sound and the
responses of fishes. Popper et al. (2003/
2004) also published a paper that
reviews the effects of anthropogenic
sound on the behavior and physiology
of fishes.
The level of sound at which a fish
will react or alter its behavior is usually
well above the detection level. Fish
have been found to react to sounds
when the sound level increased to about
20 dB above the detection level of 120
dB (Ona, 1988); however, the response
threshold can depend on the time of
year and the fish’s physiological
condition (Engas et al., 1993). In
general, fish react more strongly to
pulses of sound rather than a
continuous signal (Blaxter et al., 1981),
and a quicker alarm response is elicited
when the sound signal intensity rises
rapidly compared to sound rising more
slowly to the same level.
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Investigations of fish behavior in
relation to vessel noise (Olsen et al.,
1983; Ona, 1988; Ona and Godo, 1990)
have shown that fish react when the
sound from the engines and propeller
exceeds a certain level. Avoidance
reactions have been observed in fish
such as cod and herring when vessels
approached close enough that received
sound levels are 110 dB to 130 dB
(Nakken, 1992; Olsen, 1979; Ona and
Godo, 1990; Ona and Toresen, 1988).
However, other researchers have found
that fish such as polar cod, herring, and
capelin are often attracted to vessels
(apparently by the noise) and swim
toward the vessel (Rostad et al., 2006).
Typical sound source levels of vessel
noise in the audible range for fish are
150 dB to 170 dB (Richardson et al.,
1995).
Carlson (1994), in a review of 40 years
of studies concerning the use of
underwater sound to deter salmonids
from hazardous areas at hydroelectric
dams and other facilities, concluded
that salmonids were able to respond to
low-frequency sound and to react to
sound sources within a few feet of the
source. He speculated that the reason
that underwater sound had no effect on
salmonids at distances greater than a
few feet is because they react to water
particle motion/acceleration, not sound
pressures. Detectable particle motion is
produced within very short distances of
a sound source, although sound
pressure waves travel farther.
Potential Impacts to the Benthic
Environment
SAE’s seismic survey requires the
deployment of a submersible recording
system in the inter-tidal and marine
zones. An autonomous ‘‘nodal’’ (i.e., no
cables) system would be placed on the
seafloor by specific vessels in lines
parallel to each other with a node line
spacing of 402 m (0.25 mi). Each nodal
‘‘patch’’ will have 32 node lines parallel
to each other. The lines generally run
perpendicular to the shoreline. An
entire patch will be placed on the
seafloor prior to airgun activity. As the
patches are surveyed, the node lines
will be moved either side to side or
inline to the next location. Placement
and retrieval of the nodes may cause
temporary and localized increases in
turbidity on the seafloor. The substrate
of Cook Inlet consists of glacial silt,
clay, cobbles, pebbles, and sand
(Sharma and Burrell, 1970). Sediments
like sand and cobble dissipate quickly
when suspended, but finer materials
like clay and silt can create thicker
plumes that may harm fish; however,
the turbidity created by placing and
removing nodes on the seafloor will
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settle to background levels within
minutes after the cessation of activity.
In addition, seismic noise will radiate
throughout the water column from
airguns and pingers until it dissipates to
background levels. No studies have
demonstrated that seismic noise affects
the life stages, condition, or amount of
food resources (fish, invertebrates, eggs)
used by marine mammals, except when
exposed to sound levels within a few
meters of the seismic source or in few
very isolated cases. NMFS has also
required a seasonal closure near the
Susitna River Delta from April 15 to
October 15, which is an essential
foraging location for Cook Inlet belugas.
Where fish or invertebrates did respond
to seismic noise, the effects were
temporary and of short duration.
Consequently, disturbance to fish
species due to the activities associated
with the seismic survey (i.e, placement
and retrieval of nodes and noise from
sound sources) will be short term and
fish will be expected to return to their
pre-disturbance behavior once seismic
survey activities cease.
Based on the preceding discussion,
the activity is not expected to have any
habitat-related effects that could cause
significant or long-term consequences
for individual marine mammals or their
populations.
Mitigation
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 impact on such species or
stock and its habitat, paying particular
attention to rookeries, mating grounds,
and areas of similar significance, and on
the availability of such species or stock
for taking for certain subsistence uses
(where relevant).
Mitigation Measures in SAE’s
Application
For the mitigation measures, SAE
listed the following protocols to be
implemented during its seismic survey
program in Cook Inlet.
1. Operation of Mitigation Airgun at
Night
SAE will conduct both daytime and
nighttime operations. Nighttime
operations will be initiated only if a
‘‘mitigation airgun’’ (typically the 10
in3) has been continuously operational
from the time that PSO monitoring has
ceased for the day. Seismic activity will
not ramp up from an extended shutdown (i.e., when the airgun has been
down with no activity for at least 10
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minutes) during nighttime operations,
and survey activities will be suspended
until the following day. At night, the
vessel captain and crew will maintain
lookout for marine mammals and will
order the airgun(s) to be shut down if
marine mammals are observed in or
about to enter the established exclusion
zones.
2. Exclusion and Disturbance Zones
SAE will establish exclusion zones to
avoid Level A harassment (‘‘injury
exclusion zone’’) of all marine mammals
and to avoid Level B harassment
(‘‘disturbance exclusion zone’’) of any
beluga whales or groups of five or more
killer whales or harbor porpoises
detected within the designated zones.
The injury exclusion zone will
correspond to the area around the
source within which received levels
equal or exceed 180 dB re 1 mPa [rms]
for cetaceans and 190 dB re 1 mPa [rms]
for pinnipeds, and SAE will shut down
or power down operations if any marine
mammals are seen approaching or
entering this zone (more detail below).
The disturbance exclusion zone will
correspond to the area around the
source within which received levels
equal or exceed 160 dB re 1 mPa [rms]
and SAE will implement power down
and/or shutdown measures, as
appropriate, if any beluga whales,
humpback whales, Steller sea lions, or
group of five or more killer whales or
harbor porpoises are seen entering or
approaching the disturbance exclusion
zone.
3. Power Down and Shutdown
Procedures
A power down is the immediate
reduction in the number of operating
energy sources from a full array firing to
a mitigation airgun. A shutdown is the
immediate cessation of firing of all
energy sources. The arrays will be
immediately powered down whenever a
marine mammal is sighted approaching
close to or within the applicable
exclusion zone of the full arrays but is
outside the applicable exclusion zone of
the single source. If a marine mammal
is sighted within the applicable
exclusion zone of the single energy
source, the entire array will be
shutdown (i.e., no sources firing).
Following a power down or a shutdown,
airgun activity will not resume until the
marine mammal has clearly left the
applicable injury or disturbance
exclusion zone. The animal will be
considered to have cleared the zone if
it: (1) Is visually observed to have left
the zone; (2) has not been seen within
the zone for 15 minutes in the case of
pinnipeds and small odontocetes; or (3)
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has not been seen within the zone for
30 minutes in the case of large
odontocetes, including killer whales
and belugas.
Visual monitoring by qualified PSOs
will continue for 30 minutes after a
shutdown or at the end of a period of
seismic surveying to monitor for
animals returning to the previously
ensonified area.
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4. Ramp-Up Procedures
A ramp-up of an airgun array provides
a gradual increase in sound levels, and
involves a step-wise increase in the
number and total volume of air guns
firing until the full volume is achieved.
The purpose of a ramp-up (or ‘‘soft
start’’) is to ‘‘warn’’ cetaceans and
pinnipeds in the vicinity of the airguns
and to provide the time for them to
leave the area and thus avoid any
potential injury or impairment of their
hearing abilities.
During the seismic survey, the seismic
operator will ramp up the airgun array
slowly at a rate of no more than 6 dB
per 5-minute period. Ramp-up is used at
the start of airgun operations, after a
power- or shut-down, and after any
period of greater than 10 minutes in
duration without airgun operations
(‘‘extended shutdown’’).
A full ramp-up after a shutdown will
not begin until there has been a
minimum of 30 minutes of observation
of the applicable exclusion zone by
PSOs to assure that no marine mammals
are present. The entire exclusion zone
must be visible during the 30-minute
lead-in to a full ramp up. If the entire
exclusion zone is not visible, then rampup from a cold start cannot begin. If a
marine mammal(s) is sighted within the
injury exclusion zone during the 30minute watch prior to ramp-up, rampup will be delayed until the marine
mammal(s) is sighted outside of the
zone or the animal(s) is not sighted for
at least 15–30 minutes: 15 minutes for
small odontocetes and pinnipeds (e.g.
harbor porpoises, harbor seals, and
Steller sea lions), or 30 minutes for large
odontocetes (e.g., killer whales and
beluga whales).
5. Speed or Course Alteration
If a marine mammal is detected
outside the injury exclusion zone and,
based on its position and the relative
motion, is likely to enter that zone, the
vessel’s speed and/or direct course may,
when practical and safe, be changed to
avoid the marine mammal and also
minimize the effect on the seismic
program. This can be used in
coordination with a power down
procedure. The marine mammal
activities and movements relative to the
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seismic and support vessels will be
closely monitored to ensure that the
marine mammal does not approach
within the applicable exclusion radius.
If the mammal appears likely to enter
the exclusion radius, further mitigative
actions will be taken, i.e., either further
course alterations, power down, or shut
down of the airgun(s).
6. Measures for Beluga Whales and
Groups of Killer Whales and Harbor
Porpoises
The following are additional
protective measures for beluga whales
and groups of five or more killer whales
and harbor porpoises. Specifically, a
160-dB vessel monitoring zone will be
established and monitored in Cook Inlet
during all seismic surveys. If a beluga
whale or groups of five or more killer
whales and/or harbor porpoises are
visually sighted approaching or within
the 160-dB disturbance zone, survey
activity will not commence until the
animals are no longer present within the
160-dB disturbance zone. Whenever any
beluga whales or groups of five or more
killer whales and/or harbor porpoises
are detected approaching or within the
160-dB disturbance zone, the airguns
may be powered down before the
animal is within the 160-dB disturbance
zone, as an alternative to a complete
shutdown. If a power down is not
sufficient, the sound source(s) will be
shut-down until the animals are no
longer present within the 160-dB zone.
Additional Mitigation Measures
Required by NMFS
In addition to the mitigation measures
above, NMFS requires implementation
of the following mitigation measures.
SAE will not operate airguns within
10 miles (16 km) of the mean higher
high water (MHHW) line of the Susitna
Delta (Beluga River to the Little Susitna
River) between April 15 and October 15.
The purpose of this mitigation measure
is to protect beluga whales in the
designated critical habitat in this area
that is important for beluga whale
feeding and calving during the spring
and fall months. The range of the
setback required by NMFS was
designated to protect this important
habitat area and also to create an
effective buffer where sound does not
encroach on this habitat. This seasonal
exclusion will be in effect from April
15-October 15. Activities may occur
within this area from October 16–April
14.
A ‘‘mitigation airgun’’ (10in3) will be
operated at approximately one shot per
minute, only during daylight and when
there is good visibility, and will not be
operated for longer than 3 hours in
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duration. In cases when the next startup after the turn is expected to be
during lowlight or low visibility, use of
the mitigation airgun may be initiated
30 minutes before darkness or low
visibility conditions occur and may be
operated until the start of the next
seismic acquisition line. The mitigation
gun must still be operated at
approximately one shot per minute.
When nighttime operations ramp up
from the mitigation airgun, SAE will be
required to use passive acoustic
monitoring for at least 30 minutes prior
to ramp-up to detect beluga whales,
humpback whales, and Steller sea lions
that may be within the 160dB
disturbance zone. The support vessel
must remain sufficiently distant from
the seismic source vessel to ensure that
beluga whales, if present and vocalizing,
can be detected. Passive acoustic
monitoring must continue throughout
seismic operations occurring between
local sunset and sunrise.
NMFS requires that SAE must
suspend seismic operations if a live
marine mammal stranding is reported in
Cook Inlet coincident to, or within 72
hours of, seismic survey activities
involving the use of airguns (regardless
of any suspected cause of the stranding).
The shutdown must occur if the animal
is within a distance two times that of
the 160 dB isopleth of the largest airgun
array configuration in use. This distance
was chosen to create an additional
buffer beyond the distance at which
animals would typically be considered
harassed, as animals involved in a live
stranding event are likely compromised,
with potentially increased susceptibility
to stressors, and the goal is to decrease
the likelihood that they are further
disturbed or impacted by the seismic
survey, regardless of what the original
cause of the stranding event was.
Shutdown procedures will remain in
effect until NMFS determines and
advises SAE that all live animals
involved in the stranding have left the
area (either of their own volition or
following herding by responders).
Finally, NMFS requires that if any
marine mammal species are
encountered during seismic activities
for which take is not authorized, and are
likely to be exposed to sound pressure
levels (SPLs) greater than or equal to
160 dB re 1 mPa (rms), then SAE must
alter speed or course, power down or
shut down the sound source to avoid
take of those species.
Mitigation Conclusions
NMFS has carefully evaluated SAE’s
mitigation measures and considered a
range of other measures in the context
of ensuring that NMFS prescribes the
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means of aeffecting the least practicable
adverse impact on the affected marine
mammal species and stocks and their
habitat. Our evaluation of mitigation
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 measures are
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.
Any mitigation measure(s) prescribed
by NMFS should be able to accomplish,
have a reasonable likelihood of
accomplishing (based on current
science), or contribute to the
accomplishment of one or more of the
general goals listed below:
1. Avoidance or minimization of
injury or death of marine mammals
wherever possible (goals 2, 3, and 4 may
contribute to this goal).
2. A reduction in the numbers of
marine mammals (total number or
number at biologically important time
or location) exposed to received levels
of seismic airguns, or other activities
expected to result in the take of marine
mammals (this goal may contribute to 1,
above, or to reducing harassment takes
only).
3. A reduction in the number of times
(total number or number at biologically
important time or location) individuals
would be exposed to received levels of
seismic airguns or other activities
expected to result in the take of marine
mammals (this goal may contribute to 1,
above, or to reducing harassment takes
only).
4. A reduction in the intensity of
exposures (either total number or
number at biologically important time
or location) to received levels of seismic
airguns or other activities expected to
result in the take of marine mammals
(this goal may contribute to 1, above, or
to reducing the severity of harassment
takes only).
5. Avoidance or minimization of
adverse effects to marine mammal
habitat, paying special attention to the
food base, activities that block or limit
passage to or from biologically
important areas, permanent destruction
of habitat, or temporary destruction/
disturbance of habitat during a
biologically important time.
6. For monitoring directly related to
mitigation—an increase in the
probability of detecting marine
mammals, thus allowing for more
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effective implementation of the
mitigation.
Based on our evaluation of the
applicant’s mitigation measures, as well
as other measures considered by NMFS,
NMFS has determined that the
mitigation measures provide the means
of effecting the least practicable adverse
impact on marine mammals species or
stocks and their habitat, paying
particular attention to rookeries, mating
grounds, and areas of similar
significance.
Monitoring and Reporting
Monitoring Measures
1. Visual Vessel-based Monitoring
Vessel-based monitoring for marine
mammals will be done by experienced
PSOs throughout the period of marine
survey activities. PSOs will monitor the
occurrence and behavior of marine
mammals near the survey vessel during
all daylight periods (nautical dawn to
nautical dusk) during operation and
during most daylight periods when
airgun operations are not occurring.
PSO duties will include watching for
and identifying marine mammals,
recording their numbers, distances, and
reactions to the survey operations, and
documenting observed ‘‘take by
harassment’’ as defined by NMFS.
A minimum number of seven PSOs
(two per source vessel and two per
support vessel, with one additional PSO
on the mitigation vessel to operate the
hydrophone) will be required onboard
the survey vessel to meet the following
criteria: (1) 100 percent monitoring
coverage during all periods of survey
operations in daylight (nautical twilightdawn to nautical twilight-dusk; (2)
maximum of 4 consecutive hours on
watch per PSO; and (3) maximum of 12
hours of watch time per day per PSO.
PSO teams will consist of NMFSapproved field biologists. An
experienced field crew leader will
supervise the PSO team onboard the
survey vessel. SAE will have PSOs
aboard three vessels: the two source
vessels and one support vessel (M/V
Dreamcatcher). Two PSOs will be on
the source vessels, and three PSOs will
be on the support vessel to observe and
implement the exclusion, power down,
and shut down areas. When marine
mammals are about to enter or are
sighted within designated harassment
and exclusion zones, airgun or pinger
operations will be powered down (when
applicable) or shut down immediately.
The vessel-based observers will watch
for marine mammals during all periods
when sound sources are in operation
and for a minimum of 30 minutes prior
to the start of airgun or pinger
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operations after an extended shut down
as well as 30 minutes after the end of
airgun operation.
The observer(s) will watch for marine
mammals from the best available
vantage point on the source and support
vessels, typically the flying bridge. The
observer(s) will scan systematically with
the unaided eye and 7x50 reticle
binoculars, assisted by 40x80 long-range
binoculars.
All observations will be recorded in a
standardized format. When a mammal
sighting is made, the following
information about the sighting will be
recorded:
• Species, group size, age/size/sex
categories (if determinable), sighting
cue, behavior when first sighted and
after initial sighting, time of sighting,
heading (if consistent), bearing and
distance from the PSO, direction and
speed relative to vessel, apparent
reaction to activities (e.g., none,
avoidance, approach, paralleling, etc.),
closest point of approach, and
behavioral pace;
• Time, location, speed, activity of
the vessel (e.g., seismic airguns off,
pingers on, etc.), sea state, ice cover,
visibility, and sun glare; and
• The positions of other vessel(s) in
the vicinity of the PSO location.
The ship’s position, speed of support
vessels, and water temperature, water
depth, sea state, ice cover, visibility, and
sun glare will also be recorded at the
start and end of each observation watch,
every 30 minutes during a watch, and
whenever there is a change in any of
those variables.
2. Visual Shore-Based Monitoring
In addition to the vessel-based PSOs,
SAE will utilize shore-based monitoring
daily in the event of summer seismic
activity occurring nearshore to Cook
Inlet beluga Critical Habitat Area 1, to
visually monitor for marine mammals.
The shore-based PSOs will scan the area
prior to, during, and after the airgun
operations and will be in contact with
the vessel-based PSOs via radio to
communicate sightings of marine
mammals approaching or within the
project area. This communication will
allow the vessel-based observers to go
on a ‘‘heightened’’ state of alert
regarding occurrence of marine
mammals in the area and aid in timely
implementation of mitigation measures.
Reporting Measures
Immediate reports will be submitted
to NMFS if 25 belugas are detected in
the Level B disturbance exclusion zone
to evaluate and make necessary
adjustments to monitoring and
mitigation. If the number of detected
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takes for any marine mammal species is
met or exceeded, SAE will immediately
cease survey operations involving the
use of active sound sources (e.g., airguns
and pingers) and notify NMFS.
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1. Weekly Reports
SAE will submit a weekly field report
to NMFS Headquarters as well as the
Alaska Regional Office, no later than
close of business each Thursday during
the weeks when in-water seismic survey
activities take place. The weekly field
reports will summarize species detected
(number, location, distance from
seismic vessel, behavior), in-water
activity occurring at the time of the
sighting (discharge volume of array at
time of sighting, seismic activity at time
of sighting, visual plots of sightings, and
number of power downs and
shutdowns), behavioral reactions to inwater activities, and the number of
marine mammals exposed.
2. Monthly Reports
Monthly reports will be submitted to
NMFS for all months during which inwater seismic activities take place. The
monthly report will contain and
summarize the following information:
• Dates, times, locations, heading,
speed, weather, sea conditions
(including Beaufort sea state and wind
force), and associated activities during
all seismic operations and marine
mammal sightings.
• Species, number, location, distance
from the vessel, and behavior of any
sighted marine mammals, as well as
associated seismic activity (number of
power-downs and shutdowns), observed
throughout all monitoring activities.
• An estimate of the number (by
species) of: (i) Pinnipeds that have been
exposed to the seismic activity (based
on visual observation) at received levels
greater than or equal to 160 dB re 1 mPa
(rms) and/or 190 dB re 1 mPa (rms) with
a discussion of any specific behaviors
those individuals exhibited; and (ii)
cetaceans that have been exposed to the
seismic activity (based on visual
observation) at received levels greater
than or equal to 160 dB re 1 mPa (rms)
and/or 180 dB re 1 mPa (rms) with a
discussion of any specific behaviors
those individuals exhibited.
• A description of the
implementation and effectiveness of the:
(i) Terms and conditions of the
Biological Opinion’s Incidental Take
Statement (ITS); and (ii) mitigation
measures of the IHA. For the Biological
Opinion, the report shall confirm the
implementation of each Term and
Condition, as well as any conservation
recommendations, and describe their
effectiveness for minimizing the adverse
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effects of the action on ESA-listed
marine mammals.
3. Annual Reports
SAE will submit an annual report to
NMFS’s Permits and Conservation
Division within 90 days after the end of
operations on the water or at least 90
days prior to requiring a subsequent
authorization, whichever comes first.
The annual report will include:
• Summaries of monitoring effort
(e.g., total hours, total distances, and
marine mammal distribution through
the study period, accounting for sea
state and other factors affecting
visibility and detectability of marine
mammals).
• Analyses of the effects of various
factors influencing detectability of
marine mammals (e.g., sea state, number
of observers, and fog/glare).
• Species composition, occurrence,
and distribution of marine mammal
sightings, including date, water depth,
numbers, age/size/gender categories (if
determinable), group sizes, and ice
cover.
• Analyses of the effects of survey
operations.
• Sighting rates of marine mammals
during periods with and without
seismic survey activities (and other
variables that could affect detectability),
such as: (i) Initial sighting distances
versus survey activity state; (ii) closest
point of approach versus survey activity
state; (iii) observed behaviors and types
of movements versus survey activity
state; (iv) numbers of sightings/
individuals seen versus survey activity
state; (v) distribution around the source
vessels versus survey activity state; and
(vi) numbers of animals detected in the
160 dB harassment (disturbance
exclusion) zone.
NMFS will review the draft annual
report. SAE must then submit a final
annual report to the Chief, Permits and
Conservation Division, Office of
Protected Resources, NMFS, within 30
days after receiving comments from
NMFS on the draft annual report. If
NMFS has no comment on the draft
annual report, the draft report shall be
considered to be the final report.
4. Notification of Injured or Dead
Marine Mammals
In the unanticipated event that the
specified activity clearly causes the take
of a marine mammal in a manner
prohibited by this Authorization, such
as an injury (Level A harassment),
serious injury or mortality (e.g., shipstrike, gear interaction, and/or
entanglement), SAE shall immediately
cease the specified activities and
immediately report the incident to the
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29181
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS, her designees, and the Alaska
Regional Stranding Coordinators. The
report must include the following
information:
• Time, date, and location (latitude/
longitude) of the incident;
• Name and type of vessel involved;
• Vessel’s speed during and leading
up to the incident;
• Description of the incident;
• Status of all sound source use in the
24 hours preceding the incident;
• Water depth;
• Environmental conditions (e.g.,
wind speed and direction, Beaufort sea
state, cloud cover, and visibility);
• Description of all marine mammal
observations in the 24 hours preceding
the incident;
• Species identification or
description of the animal(s) involved;
• Fate of the animal(s); and
• Photographs or video footage of the
animal(s) (if equipment is available).
Activities shall not resume until
NMFS is able to review the
circumstances of the prohibited take.
NMFS shall work with SAE to
determine what is necessary to
minimize the likelihood of further
prohibited take and ensure MMPA
compliance. SAE may not resume their
activities until notified by NMFS via
letter or email, or telephone.
In the event that SAE discovers an
injured or dead marine mammal, and
the lead PSO determines that the cause
of the injury or death is unknown and
the death is relatively recent (i.e., in less
than a moderate state of decomposition
as described in the next paragraph), SAE
will immediately report the incident to
the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, her
designees, and the NMFS Alaska
Stranding Hotline. The report must
include the same information identified
in the paragraph above. Activities may
continue while NMFS reviews the
circumstances of the incident. NMFS
will work with SAE to determine
whether modifications in the activities
are appropriate.
In the event that SAE discovers an
injured or dead marine mammal, and
the lead PSO determines that the injury
or death is not associated with or related
to the authorized activities (e.g.,
previously wounded animal, carcass
with moderate to advanced
decomposition, or scavenger damage),
SAE shall report the incident to the
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS, her designees, the NMFS Alaska
Stranding Hotline, and the Alaska
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Regional Stranding Coordinators within
24 hours of the discovery. SAE shall
provide photographs or video footage (if
available) or other documentation of the
stranded animal sighting to NMFS and
the Marine Mammal Stranding Network.
Activities may continue while NMFS
reviews the circumstances of the
incident.
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Monitoring Results From Previously
Authorized Activities
While SAE has previously applied for
Authorizations for work in Cook Inlet,
Alaska, work was not conducted upon
receiving the Authorization. SAE has
previously conducted work under
Incidental Harassment Authorizations
in the Beaufort Sea.
Estimated Take by Incidental
Harassment
Except with respect to certain
activities not pertinent here, section
3(18) of the MMPA defines
‘‘harassment’’ as: Any act of pursuit,
torment, or annoyance which (i) has the
potential to injure a marine mammal or
marine mammal stock in the wild; or (ii)
has the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment]. Only take by Level B
behavioral harassment is anticipated as
a result of the seismic survey program
with mitigation measures. Anticipated
impacts to marine mammals are
associated with noise propagation from
the sound sources (e.g., airguns and
pingers) used in the seismic survey; no
take is expected to result from vessel
strikes because of the slow speed of the
vessels (4–5 knots).
SAE requests authorization to take
nine marine mammal species by Level
B harassment. These nine marine
mammal species are: Cook Inlet beluga
whale; humpback whale; minke whale;
killer whale; harbor porpoise; Dall’s
porpoise; gray whale; harbor seal; and
Steller sea lion.
For impulse sounds, such as those
produced by airgun(s) used in the
seismic survey, NMFS uses the 160 dB
re 1 mPa (rms) isopleth to indicate the
onset of Level B harassment. The
current Level A (injury) harassment
threshold is 180 dB (rms) for cetaceans
and 190 dB (rms) for pinnipeds. The
NMFS annual aerial survey data from
2002–2012 was used to derive density
estimates for each species (number of
individuals/km2), and is a large source
of the data in the Goetz et al 2012 model
used for beluga density estimation in
this Authorization.
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Applicable Zones for Estimating ‘‘Take
by Harassment’’
To estimate potential takes by Level B
harassment for this Authorization, as
well as for mitigation radii to be
implemented by PSOs, ranges to the 160
dB (rms), 180 dB, and 190 dB isopleths
were estimated at three different water
depths (5 m, 25 m, and 45 m) . The
distances to this threshold for the
nearshore survey locations are provided
in Table 4 in SAE’s application. The
distances to the thresholds provided in
Table 4 in SAE’s application correspond
to the broadside and endfire directions.
Compared to the airguns, the relevant
isopleths for the positioning pinger are
quite small. The distances to the 190,
180, and 160 dB (rms) isopleths are 1 m,
3 m, and 25 m (3.3, 10, and 82 ft),
respectively.
Estimates of Marine Mammal Density
SAE used one method to estimate
densities for Cook Inlet beluga whales
and another method for the other
marine mammals in the area expected to
be taken by harassment. Both methods
are described in this document.
1. Beluga Whale Density Estimates
In similar fashion to a previous IHA
issued to Apache, SAE used a habitatbased model developed by Goetz et al.
(2012a). Information from that model
has once again been used to estimate
densities of beluga whales in Cook Inlet
and we consider it to be the best
available information on beluga density.
A summary of the model is provided
here, and additional detail can be found
in Goetz et al. (2012a). To develop
NMML’s estimated densities of belugas,
Goetz et al. (2012a) developed a model
based on aerial survey data, depth
soundings, coastal substrate type,
environmental sensitivity index,
anthropogenic disturbance, and
anadromous fish streams to predict
beluga densities throughout Cook Inlet.
The result of this work is a beluga
density map of Cook Inlet, which easily
sums the belugas predicted within a
given geographic area. NMML
developed its predictive habitat model
from the distribution and group size of
beluga whales observed between 1994
and 2008. A 2-part ‘‘hurdle’’ model (a
hurdle model in which there are two
processes, one generating the zeroes and
one generating the positive values) was
applied to describe the physical and
anthropogenic factors that influence (1)
beluga presence (mixed model logistic
regression) and (2) beluga count data
(mixed model Poisson regression).
Beluga presence was negatively
associated with sources of
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anthropogenic disturbance and
positively associated with fish
availability and access to tidal flats and
sandy substrates. Beluga group size was
positively associated with tidal flats and
proxies for seasonally available fish.
Using this analysis, Goetz et al. (2012)
produced habitat maps for beluga
presence, group size, and the expected
number of belugas in each 1 km2 cell of
Cook Inlet. The habitat-based model
developed by NMML uses a Geographic
Information System (GIS). A GIS is a
computer system capable of capturing,
storing, analyzing, and displaying
geographically referenced information;
that is, data identified according to
location. However, the Goetz et al.
(2012) model does not incorporate
seasonality into the density estimates.
Rather, SAE factors in seasonal
considerations of beluga density into the
design of the survey tracklines and
locations (as discussion in more detail
later in this document) in addition to
other factors such as weather, ice
conditions, and seismic needs.
2. Non-Beluga Whale Species Density
Estimates
Densities of other marine mammal
species in the project area were
estimated from the annual aerial surveys
conducted by NMFS for Cook Inlet
beluga whale between 2000 and 2012 in
June (Rugh et al., 2000, 2001, 2002,
2003, 2004b, 2005b, 2006, 2007;
Shelden et al., 2008, 2009, 2010, 2012;
Hobbs et al., 2011). These surveys were
flown in June to collect abundance data
of beluga whales, but sightings of other
marine mammals were also reported.
Although these data were only collected
in one month each year, these surveys
provide the best available relatively long
term data set for sighting information in
the project area. The general trend in
marine mammal sighting is that beluga
whales and harbor seals are the species
seen most frequently in upper Cook
Inlet, with concentrations of harbor
seals near haul out sites on Kalgin
Island and of beluga whales near river
mouths, particularly the Susitna River.
The other marine mammals of interest
for this authorization (humpback
whales, gray whales, minke whales,
killer whales, harbor porpoises, Dall’s
porpoises, Steller sea lions) are observed
infrequently in upper Cook Inlet and
more commonly in lower Cook Inlet. In
addition, these densities are calculated
based on a relatively large area that was
surveyed, much larger than the
proposed area for a given year of seismic
data acquisition. Furthermore, these
annual aerial surveys are conducted
only in June (numbers from August
surveys were not used because the area
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surveyed was not provided), so it does
not account for seasonal variations in
distribution or habitat use of each
species.
Table 5 in SAE’s application provides
a summary of the results of NMFS aerial
survey data collected in June from 2000
to 2012. To estimate density of marine
mammals, total number of individuals
(other species) observed for the entire
survey area by year (surveys usually last
several days) was divided by the
approximate total area surveyed for each
year (density = individuals/km2). As
noted previously, the total number of
animals observed for the entire survey
includes both lower and upper Cook
Inlet, so the total number reported and
used to calculate density is higher than
the number of marine mammals
anticipated to be observed in the project
area. In particular, the total number of
harbor seals observed on several surveys
is very high due to several large haul
outs in lower and middle Cook Inlet.
The table below (Table 2) provides
average density estimates for gray
whales, harbor seals, harbor porpoises,
killer whales, and Steller sea lions over
the 2000–2012 period.
TABLE 2—ANIMAL DENSITIES IN COOK
INLET
Average density
(animals/km2)
Species
Humpback whale ......
Gray whale ................
Minke whale ..............
Killer whale ................
Dall’s porpoise ..........
Harbor porpoise ........
Harbor seal ...............
Steller sea lion ..........
0.0024
9.45E–05
1.14E–05
0.0008
0.0002
0.0033
0.28
0.008
Calculation of Takes by Harassment
1. Beluga Whales
As a result of discussions with NMFS,
SAE has used the NMML model (Goetz
et al., 2012a) for the estimate of takes in
this Authorization. SAE has established
two zones (Zone 1 and Zone 2) and
proposes to conduct seismic surveys
within all, or part of these zones; to be
determined as weather, ice, and
priorities dictate, which can be found in
the attached figure which will be posted
at https://www.nmfs.noaa.gov/pr/
permits/incidental/oilgas.htm
Based on information using Goetz et
al. model (2012a), SAE derived one
density estimate for beluga whales in
Upper Cook Inlet (i.e., north of the
Forelands) and another density estimate
for beluga whales in Lower Cook Inlet
(i.e., south of the Forelands). The
density estimate for Upper Cook Inlet is
0.0212 and is 0.0056 for Lower Cook
Inlet. SAE’s seismic operational area
will be determined as weather, ice, and
priorities dictate. SAE has requested a
maximum allowed take for Cook Inlet
beluga whales of 30 individuals. SAE
will operate in a portion of the total
seismic operation area of 3,934 km2
(1,519 mi2), such that when one
multiplies the anticipated beluga whale
density based on the seismic survey
operational area times the area to be
ensonified to the 160-dB isopleth of 9.5
km (5.9 mi) and takes the number of
days into consideration, estimated takes
will not exceed 30 beluga whales.
In order to estimate when that level is
reached, SAE is using a formula based
on the total potential area of each
seismic survey project zone (including
the 160 dB buffer) and the average
density of beluga whales for each zone.
Daily take is calculated as the product
of a daily ensonified area times the
density in that area. Then daily take is
summed across all the days of the
survey until the survey approaches 30
takes.
TABLE 3—EXPECTED BELUGA WHALE TAKES, TOTAL AREA OF ZONE, AND AVERAGE BELUGA WHALE DENSITY ESTIMATES
Expected Beluga
takes from
NMML model
(including the
160 dB buffer)
Zone 1—Upper Inlet .....................................................................................................
Zone 2—Lower Inlet .....................................................................................................
Total area of zone
(km2)
(including the
160 dB buffer)
28
29
2,126
1,808
Average take
density
(dx)
d1 = 0.0212
d2 = 0.0056
application) to ensure a maximum of 30
beluga takes during the open water
season. In order to ensure that SAE does
not exceed 30 beluga whale takes, the
following equation is being used:
This formula also allows SAE to have
flexibility to prioritize survey locations
in response to local weather, ice, and
operational constraints. SAE may
choose to survey portions of a zone or
a zone in its entirety, and the analysis
in this Authorization takes this into
account. Using this formula, if SAE
surveys the entire area of Zone 1 (1,319
km2), then essentially none of Zone 2
will be surveyed because the input in
the calculation denoted by d2A2 will
essentially need to be zero to ensure that
the total allotted take of beluga whales
is not exceeded. The use of this formula
will ensure that SAE’s seismic survey
will not exceed 30 calculated beluga
takes.
Operations are required to cease once
SAE has conducted seismic data
acquisition in an area where
multiplying the applicable density by
the total ensonified area out to the 160dB isopleth equaled 30 beluga whales,
using the equation provided above. If 30
belugas are visually observed before the
calculation reaches 30 belugas, SAE is
also required to cease survey activity.
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2. Humpback Whales
Although the density for humpback
whales in Cook Inlet according to
NMML surveys is 0.0024 animals per
km2, it is widely known that humpbacks
occur with greater frequency in the
lower inlet, and are rarely sighted in the
upper inlet. Apache data has indicated
that take of two humpback whales is
possible, but existing observation data
of humpback whales in Cook Inlet
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SAE will limit surveying in the
seismic survey area (Zones 1 and 2
presented in Figures 1 and 2 of SAE’s
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supports that this is extremely unlikely.
No more than two humpback whales
have ever been recorded in a single
season by NMFS observers or PSOs on
board seismic vessels in Cook Inlet.
Therefore, while the occurrence of two
humpbacks is rare but possible, it is
unlikely that more than five humpbacks
will be exposed by Level B harassment
based on known distribution of
humpbacks in Cook Inlet.
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3. Steller Sea Lions
The density estimate used in the
Authorization for Steller sea lions
included NMFS data that includes
animals at sea lion haulouts that are
within Cook Inlet, but are well south of
the action area. An anomalous sighting
of 20 animals occurred along the
southern edge of the action area, far
from any known haulouts or rookeries
(such a large congregation of Steller sea
lions far from haulouts or rookeries is
unusual) which is included in NMFS’
revised estimate of Steller sea lion take,
but does not include animals observed
outside of the action area. Based on
monitoring reports of other seismic
activities in Cook Inlet, there are
typically one or two Steller sea lions
within the action area per year. Two
individuals were observed by Apache
PSOs in 2014 and three groups totaling
about four animals were observed in
2012. Because of this data, NMFS has
revised its take estimate to 25
individuals, which will account for
what one may expect seismic vessels
implementing mitigation measures to
encounter in a year, but allows for the
possibility that the survey may
encounter an anomalously large group
such as was observed by NMFS aerial
observers near the southern portion of
the action area in 2006.
While the NMML survey data reports
an average density of 0.008281 Steller
sea lions per km2 in the action area,
NMFS aerial survey data indicate a
maximum density of 0.003518 Steller
sea lions per km2 with in the action area
(20 animals/5,684 km2). Given the size
and location of the action area, we have
determined that authorizing take of 25
Steller sea lions is most appropriate and
reflects appropriate use of the best
available scientific data.
4. Harbor seals
As noted above, using the daily
ensonified area × number of survey days
× density method results in a reasonable
estimate of the instances of take, but
likely significantly overestimates the
number of individual animals expected
to be taken. With most species, even this
overestimated number is still very
small, and additional analysis is not
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really necessary to ensure minor
impacts. However, because of the
number and density of harbor seals in
the area, a more accurate understanding
of the number of individuals likely
taken is necessary to fully analyze the
impacts and ensure that the total
number of harbor seals taken is small.
As described below, we believe that
the modeled number of estimated
instances of take referenced above may
actually be high, based on monitoring
results from the area. The density
estimate from NMFS aerial surveys
includes harbor seal haulouts far south
of the action area that may never move
to an ensonified area. Further, we
believe that we can reasonably estimate
the comparative number of individual
harbor seals that will likely be taken,
based both on monitoring data,
operational information, and an a
general understanding of harbor seal
habitat use.
Using the daily ensonified area ×
number of survey days × density
formula (based on surveying 6.7 source
lines per day), the number of instances
of exposure above the 160-dB threshold
estimated for SAE’s activity in Cook
Inlet is 19,315. However, when we
examine monitoring data from previous
activities, it is clear this number is an
overestimate—compared to both aerial
and vessel based observation efforts.
Apache’s monitoring report from 2012
details that they saw 2,474 harbor seals
from 29 aerial flights (over 29 days) in
the vicinity of the survey during the
month of June, which is the peak month
for harbor seal haulout. In surveying the
literature, correction factors to account
for harbor seals in water based on land
counts vary from 1.2 to 1.65 (CITE).
Using the most conservative factor of
1.65 (allowing us to consider that some
of the other individuals on land may
have entered the water at other points
in day), if Apache saw 2,474 seals
hauled out then there were an estimated
1,500 seals in the water during those 29
days. If, because there were only 29
surveys, we conservatively multiply by
5.5 to estimate the number of seals that
might have been seen if the aerial
surveys were conducted for 160 days,
this yields an estimate of 8,250
instances of seal exposure in the water,
which is far less than the estimated
19,315. That the number of potential
instances of exposure is likely less than
19,315 is also supported by the visual
observations from PSOs on board
vessels. PSOs sighted a total of 285 seals
in water over 147 days of activity which
would rise to about 310 is adjusted to
reflect 160 days of effort. Given the size
of the disturbance zone for these
activities, it is likely that not all harbor
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seals that were exposed were seen by
PSOs, however 310 is still far less than
the estimate of 19,315 given by the
density calculations.
Further, based on the residential
nature of harbor seals and the number
of patches SAE plans to shoot, it is
possible to reasonably estimate the
number of individual harbor seals
exposed, given the instances of
exposures. Based on an estimate of 32
patches in 160 days, SAE will shoot one
patch in 5 days. If seals are generally
returning to haulouts in the survey area
over the 5 days of any given patch
shoot, than any given seal in the area
could be exposed a minimum of one day
and a maximum of all five days, with an
average of 3 days. If the original
exposure estimate using density is
19,315 exposures, then when divided by
three (the average number of times an
animal could be exposed during the
shooting of one patch), the expected
number of individuals exposed is 6,438,
which is approximately 28% of the
population. This number is also likely
an overestimate given that adjoining
patches may be shot, meaning the same
seals could be exposed over multiple
patches. Given these multiple methods,
as well as the behavioral preferences of
harbor seals for haulouts in certain parts
of the Inlet (Montgomery et al., 2007),
and high concentrations at haulouts in
the lower Inlet (Boveng et al.), it is
unreasonable to expect that more than
25% of the population, or 5,725
individuals, will be taken by Level B
harassment during SAE’s activity.
5. Other Marine Mammal Species
The estimated takes of other Cook
Inlet marine mammals that may be
potentially harassed during the seismic
surveys was calculated by multiplying
the following:
• Average density estimates (derived
from NMFS aerial surveys from 2000–
2012 and presented in Table 3 in this
document)
• the area ensonified by levels ≥160
dB re mPa rms in one day (calculated
using the total ensonified area per day
of 414.92 km2, which is derived by
applying the buffer distance to the 160
dB isopleth to the area of 6 survey
tracklines),
• the number of potential survey days
(160).
This equation provides the number of
instances of take that will occur in the
duration of the survey, but
overestimates the number of individual
animals taken because not every
exposure on every successive day is
expected to be a new individual.
Especially with resident species, re-
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exposures of individuals are expected
across the months of the survey.
SAE anticipates that a crew will
collect seismic data for 8–10 hours per
day over approximately 160 days over
the course of 8 to 9 months each year.
It is assumed that over the course of
these 160 days, no more than 777 km2
will be surveyed in total, but areas can
be surveyed more than once. It is
important to note that environmental
conditions (such as ice, wind, fog) will
play a significant role in the actual
operating days; therefore, these
estimates are conservative in order to
provide a basis for probability of
encountering these marine mammal
species in the project area.
Summary of Level B Harassment Takes
Table 4 outlines the density estimates
used to estimate Level B harassment
takes, the requested Level B harassment
take levels, the abundance of each
species in Cook Inlet, the percentage of
each species or stock estimated to be
taken, and current population trends.
TABLE 4—DENSITY ESTIMATES, LEVEL B HARASSMENT TAKE LEVELS, SPECIES OR STOCK ABUNDANCE, PERCENTAGE OF
POPULATION TO BE TAKEN, AND SPECIES TREND STATUS
Percentage of
population
Species
Average density
(#individuals/km2)
Beluga whale ...................
30
312 ..................................
9.6
Humpback whale .............
Upper=0.0212;
Lower=0.0056.
0.0024 .............................
5
7,469 ...............................
0.067
Minke whale .....................
Gray whale .......................
Killer whale ......................
1.14E–05 ........................
5.33E–05 ........................
0.00082 ...........................
1
7
55
1,233 ...............................
19,126 .............................
2,347 (resident) ..............
345 (transient) ................
0.06
0.033
2.34
15.9
Harbor porpoise ...............
Dall’s porpoise .................
Harbor seal ......................
Steller sea lion .................
0.0033 .............................
0.0002 .............................
0.28 .................................
0.0082 .............................
219
14
5,725
25
31,046
83,400
22,900
45,649
0.70
0.016
25
0.055
Analyses and Determinations
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Negligible Impact Analysis
Negligible impact is ‘‘an impact
resulting from the specified activity that
cannot be reasonably expected to, and is
not reasonably likely to, adversely affect
the species or stock through effects on
annual rates of recruitment or survival’’
(50 CFR 216.103). A negligible impact
finding is based on the lack of likely
adverse effects on annual rates of
recruitment or survival (i.e., populationlevel effects). An estimate of the number
of 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,
feeding, migration, etc.), as well as the
number and nature of estimated Level A
harassment takes, the number of
estimated mortalities, effects on habitat,
and the status of the species.
To avoid repetition, the discussion of
our analyses applies to all the species
listed in Table 4, divided in some places
by group, given than the anticipated
effects of the seismic survey on marine
mammals are expected to be relatively
similar in nature. Where there is
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Level B take
Abundance
.............................
.............................
.............................
.............................
information about the size, status, or
structure of any species or stock that
would lead to a different analysus (e.g.
beluga whales), species-specific factors
have been identified. In some cases
however, we add species-specific
information regarding effects (including
on habitat) that also informed our
analysis.
Given the required mitigation and
related monitoring, no injuries or
mortalities are anticipated to occur as a
result of SAE’s seismic survey in Cook
Inlet, and none are authorized.
Additionally, animals in the area are not
expected to incur hearing impairment
(i.e., TTS or PTS) or non-auditory
physiological effects. The number of
takes that are authorized are expected to
be limited to short-term Level B
behavioral harassment. The seismic
airguns do not operate continuously
over a 24-hour period. Rather airguns
are operational for a few hours at a time
totaling about 10 hours a day.
The addition of nine vessels, and
noise due to vessel operations
associated with the seismic survey, is
not outside the present experience of
marine mammals in Cook Inlet,
although levels may increase locally.
Given the large number of vessels in
Cook Inlet and the apparent habituation
to vessels by Cook Inlet beluga whales
and the other marine mammals that may
occur in the area, vessel activity and
noise is not expected to have effects that
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Trend
Decreasing.
Southeast Alaska increasing.
No reliable information.
Stable/increasing.
Resident stock possibly
increasing.
Transient stock stable.
No reliable information.
No reliable information.
Stable.
Decreasing but with regional variability (some
stable or increasing).
could cause significant or long-term
consequences for individual marine
mammals or their populations.
Cook Inlet beluga whales, the western
DPS of Steller sea lions, and Central
North Pacific humpback whales are
listed as endangered under the ESA.
These stocks are also considered
depleted under the MMPA. The
estimated annual rate of decline for
Cook Inlet beluga whales was 0.6
percent between 2002 and 2012. Steller
sea lion trends for the western stock are
variable throughout the region with
some decreasing and others remaining
stable or even indicating slight
increases. The Central North Pacific
population of humpbacks is known to
be increasing, with different techniques
predicting abundance increases between
4.9 to 7 percent annually. The other
seven species that may be taken by
harassment during SAE’s seismic survey
program are not listed as threatened or
endangered under the ESA nor as
depleted under the MMPA.
Cetaceans. Odontocete (including
Cook Inlet beluga whales, killer whales,
and harbor porpoises) reactions to
seismic energy pulses are usually
thought to be limited to shorter
distances from the airgun(s) than are
those of mysticetes, in part because
odontocete low-frequency hearing is
assumed to be less sensitive than that of
mysticetes. Belugas in the Canadian
Beaufort Sea in summer appear to be
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fairly responsive to seismic energy, with
few being sighted within 10–20 km
(6–12 mi) of seismic vessels during
aerial surveys (Miller et al., 2005).
However, Cook Inlet belugas are more
accustomed to anthropogenic sound
than beluga whales in the Beaufort Sea.
Therefore, the results from the Beaufort
Sea surveys do not directly translate to
potential reactions of Cook Inlet beluga
whales. Also, due to the dispersed
distribution of beluga whales in Cook
Inlet during winter and the
concentration of beluga whales in upper
Cook Inlet from late April through early
fall, belugas will likely occur in small
numbers in the majority of SAE’s survey
area during the majority of SAE’s annual
operational timeframe of April through
December. For the same reason, as well
as mitigation measures, it is unlikely
that animals will be exposed to received
levels capable of causing injury.
Potential impacts to marine mammal
habitat were discussed previously in
this document (see the ‘‘Anticipated
Effects on Habitat’’ section). Although
some disturbance is possible to food
sources of marine mammals, the
impacts are anticipated to be minor
enough as to not affect annual rates of
recruitment or survival of marine
mammals in the area. Based on the size
of Cook Inlet where feeding by marine
mammals occurs versus the localized
area of the marine survey activities, any
missed feeding opportunities in the
direct project area will be minor based
on the fact that other feeding areas exist
elsewhere. Taking into account the
mitigation measures that are planned,
effects on cetaceans are generally
expected to be restricted to avoidance of
a limited area around the survey
operation and short-term changes in
behavior, falling within the MMPA
definition of ‘‘Level B harassment’’.
Animals are not expected to
permanently abandon any area that is
surveyed, and any behaviors that are
interrupted during the activity are
expected to resume once the activity
ceases. Only a small portion of marine
mammal habitat will be affected at any
time, and other areas within Cook Inlet
will be available for necessary biological
functions.
In addition, of specific importance to
belugas, NMFS seasonally restricts
seismic survey operations in the area
known to be important for beluga whale
feeding, calving, or nursing. The
primary location for these biological life
functions occurs in the Susitna Delta
region of upper Cook Inlet. NMFS
proposes to implement a 16 km (10 mi)
seasonal exclusion from seismic survey
operations in this region from April 15–
October 15. The highest concentrations
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of belugas are typically found in this
area from early May through September
each year. NMFS has incorporated a 2week buffer on each end of this seasonal
use timeframe to account for any
anomalies in distribution and marine
mammal usage. Additionally, in the
event that a beluga is seen outside of the
seasonal restricted area and buffer,
seismic operations are required to shut
down if a beluga is seen anywhere in
the 160dB disturbance zone.
Mitigation measures such as
controlled vessel speed, dedicated
marine mammal observers, speed and
course alterations, and shutdowns or
power downs when marine mammals
are seen within defined ranges designed
both to avoid injury and disturbance
will further reduce short-term reactions
and minimize any effects on hearing
sensitivity. In all cases, the effects of the
seismic survey are expected to be shortterm, with no lasting biological
consequence. Therefore, the exposure of
cetaceans to SAE’s seismic survey
activity, operation is not anticipated to
have an adverse effect on annual rates
of recruitment or survival of the affected
species or stocks of cetaceans, and
therefore will have a negligible impact
on them.
Pinnipeds (harbor seals, Steller sea
lions). Some individual pinnipeds may
be exposed to sound from the seismic
surveys more than once during the
timeframe of the project. Taking into
account the mitigation measures that are
planned, effects on pinnipeds are
generally expected to be restricted to
avoidance of a limited area around the
survey operation and short-term
changes in behavior, falling within the
MMPA definition of ‘‘Level B
harassment.’’ Animals are not expected
to permanently abandon any area that is
surveyed, and any behaviors that are
interrupted during the activity are
expected to resume once the activity
ceases. Only a small portion of pinniped
habitat will be affected at any time, and
other areas within Cook Inlet will be
available for necessary biological
functions. In addition, the area where
the survey will take place is not known
to be an important location where
pinnipeds haul out. The closest known
haul-out site is located on Kalgin Island,
which is about 22 km from the
McArther River. More recently, some
large congregations of harbor seals have
been observed hauling out in upper
Cook Inlet. However, mitigation
measures, such as vessel speed, course
alteration, and visual monitoring, and
restrictions will be implemented to help
reduce impacts to the animals.
Therefore, the exposure of pinnipeds to
sounds produced by this phase of SAE’s
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Sfmt 4703
seismic survey is not anticipated to have
an adverse effect on annual rates of
recruitment or survival on those
pinniped species or stocks, and
therefore will have a negligible impact.
Based on the analysis contained
herein of the likely effects of the
specified activity on marine mammals
and their habitat, and taking into
consideration the implementation of the
monitoring and mitigation measures,
NMFS finds that SAE’s seismic survey
will have a negligible impact on the
affected marine mammal species or
stocks.
Small Numbers Analysis
The requested takes authorized
annually represent 9.6 percent of the
Cook Inlet beluga whale population of
approximately 312 animals (Allen and
Angliss, 2014), 2.34 percent of the
Alaska resident stock and 15.9 percent
of the Gulf of Alaska, Aleutian Island
and Bering Sea stock of killer whales
(1,123 residents and 345 transients),
0.70 percent of the Gulf of Alaska stock
of approximately 31,046 harbor
porpoises, 0.067 percent of the 7,469
Central North Pacific humpback whales,
0.06 percent of the 1,233 Alaska minke
whales, 0.016 percent of the 83,400 Gulf
of Alaska Dall’s porpoise, and 0.033
percent of the eastern North Pacific
stock of approximately 19,126 gray
whales. The take requests presented for
harbor seals represent 25 percent of the
Cook Inlet/Shelikof stock of
approximately 22,900 animals. The
requested takes for Steller sea lions
represent 0.055 percent of the U.S.
portion of the western stock of
approximately 45,649 animals. These
take estimates represent the percentage
of each species or stock that could be
taken by Level B behavioral harassment.
NMFS finds that any incidental take
reasonably likely to result from the
effects of the activity, as authorized to
be mitigated through this IHA, will be
limited to small numbers relative to the
affected species or stocks. In addition to
the quantitative methods used to
estimate take, NMFS also considered
qualitative factors that further support
the ‘‘small numbers’’ determination,
including: (1) The seasonal distribution
and habitat use patterns of Cook Inlet
beluga whales, which suggest that for
much of the time only a small portion
of the population will be accessible to
impacts from SAE’s activity, as most
animals are found in the Susitna Delta
region of Upper Cook Inlet from early
May through September; (2) other
cetacean species and Steller sea lions
are not common in the seismic survey
area; (3) the mitigation requirements,
which provide spatio-temporal
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limitations that avoid impacts to large
numbers of belugas feeding and calving
in the Susitna Delta and limit exposures
to sound levels associated with Level B
harassment; (4) the monitoring
requirements and mitigation measures
described earlier in this document for
all marine mammal species that will
further reduce the amount of takes; and
(5) monitoring results from previous
activities that indicated low numbers of
beluga whale sightings within the Level
B disturbance exclusion zone and low
levels of Level B harassment takes of
other marine mammals. Therefore,
NMFS determined that the numbers of
animals likely to be taken are small.
tkelley on DSK3SPTVN1PROD with NOTICES2
Impact on Availability of Affected
Species for Taking for Subsistence Uses
Relevant Subsistence Uses
The subsistence harvest of marine
mammals transcends the nutritional and
economic values attributed to the
animal and is an integral part of the
cultural identity of the region’s Alaska
Native communities. Inedible parts of
the whale provide Native artisans with
materials for cultural handicrafts, and
the hunting itself perpetuates Native
traditions by transmitting traditional
skills and knowledge to younger
generations (NOAA, 2007).
The Cook Inlet beluga whale has
traditionally been hunted by Alaska
Natives for subsistence purposes. For
several decades prior to the 1980s, the
Native Village of Tyonek residents were
the primary subsistence hunters of Cook
Inlet beluga whales. During the 1980s
and 1990s, Alaska Natives from villages
in the western, northwestern, and North
Slope regions of Alaska either moved to
or visited the south central region and
participated in the yearly subsistence
harvest (Stanek, 1994). From 1994 to
1998, NMFS estimated 65 whales per
year (range 21–123) were taken in this
harvest, including those successfully
taken for food and those struck and lost.
NMFS concluded that this number was
high enough to account for the
estimated 14 percent annual decline in
the population during this time (Hobbs
et al., 2008). Actual mortality may have
been higher, given the difficulty of
estimating the number of whales struck
and lost during the hunts. In 1999, a
moratorium was enacted (Pub. L. 106–
31) prohibiting the subsistence take of
Cook Inlet beluga whales except through
a cooperative agreement between NMFS
and the affected Alaska Native
organizations. Since the Cook Inlet
beluga whale harvest was regulated in
1999 requiring cooperative agreements,
five beluga whales have been struck and
harvested. Those beluga whales were
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harvested in 2001 (one animal), 2002
(one animal), 2003 (one animal), and
2005 (two animals). The Native Village
of Tyonek agreed not to hunt or request
a hunt in 2007, when no comanagement agreement was to be signed
(NMFS, 2008a).
On October 15, 2008, NMFS
published a final rule that established
long-term harvest limits on Cook Inlet
beluga whales that may be taken by
Alaska Natives for subsistence purposes
(73 FR 60976). That rule prohibits
harvest for a 5-year interval period if the
average stock abundance of Cook Inlet
beluga whales over the prior five-year
interval is below 350 whales. Harvest
levels for the current 5-year planning
interval (2013–2017) are zero because
the average stock abundance for the
previous five-year period (2008–2012)
was below 350 whales. Based on the
average abundance over the 2002–2007
period, no hunt occurred between 2008
and 2012 (NMFS, 2008a). The Cook
Inlet Marine Mammal Council, which
managed the Alaska Native Subsistence
fishery with NMFS, was disbanded by a
unanimous vote of the Tribes’
representatives on June 20, 2012. At this
time, no harvest is expected in 2015 or,
likely, in 2016.
Data on the harvest of other marine
mammals in Cook Inlet are lacking.
Some data are available on the
subsistence harvest of harbor seals,
harbor porpoises, and killer whales in
Alaska in the marine mammal stock
assessments. However, these numbers
are for the Gulf of Alaska including
Cook Inlet, and they are not indicative
of the harvest in Cook Inlet.
There is a low level of subsistence
hunting for harbor seals in Cook Inlet.
Seal hunting occurs opportunistically
among Alaska Natives who may be
fishing or travelling in the upper Inlet
near the mouths of the Susitna River,
Beluga River, and Little Susitna River.
Some data are available on the
subsistence harvest of harbor seals,
harbor porpoises, and killer whales in
Alaska in the marine mammal stock
assessments. However, these numbers
are for the Gulf of Alaska including
Cook Inlet, and they are not indicative
of the harvest in Cook Inlet. Some
detailed information on the subsistence
harvest of harbor seals is available from
past studies conducted by the Alaska
Department of Fish & Game (Wolfe et
al., 2009). In 2008, 33 harbor seals were
taken for harvest in the Upper KenaiCook Inlet area. In the same study,
reports from hunters stated that harbor
seal populations in the area were
increasing (28.6%) or remaining stable
(71.4%). The specific hunting regions
identified were Anchorage, Homer,
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29187
Kenai, and Tyonek, and hunting
generally peaks in March, September,
and November (Wolfe et al., 2009).
Potential Impacts on Availability for
Subsistence Uses
Section 101(a)(5)(D) also requires
NMFS to determine that the taking will
not have an unmitigable adverse effect
on the availability of marine mammal
species or stocks for subsistence use.
NMFS has defined ‘‘unmitigable adverse
impact’’ in 50 CFR 216.103 as an impact
resulting from the specified activity: (1)
That is likely to reduce the availability
of the species to a level insufficient for
a harvest to meet subsistence needs by:
(i) Causing the marine mammals to
abandon or avoid hunting areas; (ii)
Directly displacing subsistence users; or
(iii) Placing physical barriers between
the marine mammals and the
subsistence hunters; and (2) That cannot
be sufficiently mitigated by other
measures to increase the availability of
marine mammals to allow subsistence
needs to be met.
The primary concern is the
disturbance of marine mammals through
the introduction of anthropogenic sound
into the marine environment during the
seismic survey. Marine mammals could
be behaviorally harassed and either
become more difficult to hunt or
temporarily abandon traditional hunting
grounds. The other anthropogenic
activities proposed for Cook Inlet in the
2015 open water season that require an
Authorization are spread throughout the
Inlet and not concentrated in the area of
SAE’s activity, lessening the concern
about spatial overlap. However, the
seismic survey will not have any
impacts to beluga harvests as none
currently occur in Cook Inlet.
Additionally, subsistence harvests of
other marine mammal species are
limited in Cook Inlet.
Plan of Cooperation or Measures To
Minimize Impacts to Subsistence Hunts
Regulations at 50 CFR 216.104(a)(12)
require IHA applicants for activities that
take place in Arctic waters to provide a
Plan of Cooperation or information that
identifies what measures have been
taken and/or will be taken to minimize
adverse effects on the availability of
marine mammals for subsistence
purposes. The entire upper Cook unit
and a portion of the lower Cook unit
falls north of 60° N, or within the region
NMFS has designated as an Arctic
subsistence use area. There are several
villages in SAE’s project area that have
traditionally hunted marine mammals,
primarily harbor seals. Tyonek is the
only tribal village in upper Cook Inlet
with a tradition of hunting marine
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mammals, in this case harbor seals and
beluga whales. However, for either
species the annual recorded harvest
since the 1980s has averaged about one
or fewer of either species (Fall et al.
1984, Wolfe et al. 2009, SRBA and HC
2011), and there is currently a
moratorium on subsistence harvest of
belugas. Further, many of the seals that
are harvested are done incidentally to
salmon fishing or moose hunting (Fall et
al. 1984, Merrill and Orpheim 2013),
often near the mouths of the Susitna
Delta rivers (Fall et al. 1984) north of
SAE’s seismic survey area.
Villages in lower Cook Inlet adjacent
to SAE’s seismic area (Kenai, Salamatof,
and Ninilchik) have either not
traditionally hunted beluga whales, or at
least not in recent years, and rarely do
they harvest sea lions. Between 1992
and 2008, the only reported sea lion
harvests from this area were two Steller
sea lions taken by hunters from Kenai
(Wolfe et al. 2009). These villages more
commonly harvest harbor seals, with
Kenai reporting an average of about 13
per year between 1992 and 2008 (Wolfe
et al. 2009). According to Fall et al.
(1984), many of the seals harvested by
hunters from these villages were taken
on the west side of the inlet during
hunting excursions for moose and black
bears (or outside SAE’s lower Cook
unit). Although marine mammals
remain an important subsistence
resource in Cook Inlet, the number of
animals annually harvested are low, and
are primarily harbor seals. Much of the
harbor seal harvest occurs incidental to
other fishing and hunting activities, and
at areas outside of the SAE’s seismic
areas such as the Susitna Delta or the
west side of lower Cook Inlet. Also, SAE
is unlikely to conduct seismic activity
in the vicinity of any of the river mouths
where large numbers of seals haul out.
SAE has identified the following
features that are intended to reduce
impacts to subsistence users:
• In-water seismic activities will
follow mitigation procedures to
minimize effects on the behavior of
marine mammals and, therefore,
opportunities for harvest by Alaska
Native communities.
SAE and NMFS recognize the
importance of ensuring that ANOs and
federally recognized tribes are informed,
engaged, and involved during the
permitting process and will continue to
work with the ANOs and tribes to
discuss operations and activities.
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From mid-March through April 2015,
SAE met with the following
communities and organizations: Nikiski,
Ninilchik Native Association Inc.,
Tyonek Native Corporation, Tyonek
Village, Ninilchik, Nikiski Facilities
Group, and United Cook Inlet Drift
Association. These meetings were meant
to inform the audience about the project
as well as listen to concerns and
comments. There will also be a review
of permit stipulations and a permit
matrix developed for the crews. The
means of communications and contacts
list is developed and implemented into
the project, found in SAE’s Plan of
Cooperation. The use of PSOs/MMO’s
on board the vessels will ensure that
appropriate precautions are taken to
avoid harassment of marine mammals. If
a conflict does occur with project
activities involving subsistence or
fishing, the project manager will
immediately contact the affected party
to resolve the conflict. If avoidance is
not possible, the project manager will
initiate communication with the
Operations Supervisor to resolve the
issue and plan an alternative course of
action. The communications will
involve the Permits Manager and the
Anchorage Office of SAE.
Unmitigable Adverse Impact Analysis
and Determination
The project will not have any effect
on beluga whale harvests because no
beluga harvest will take place in 2015.
Additionally, the seismic survey area is
not an important native subsistence site
for other subsistence species of marine
mammals, and Cook Inlet contains a
relatively small proportion of marine
mammals utilizing Cook Inlet; thus, the
number harvested is expected to be
extremely low. The timing and location
of subsistence harvest of Cook Inlet
harbor seals may coincide with SAE’s
project, but because this subsistence
hunt is conducted opportunistically and
at such a low level (NMFS, 2013c),
SAE’s program is not expected to have
an impact on the subsistence use of
harbor seals. Moreover, the survey will
result in only temporary disturbances.
Accordingly, the specified activity will
not impact the availability of these other
marine mammal species for subsistence
uses.
NMFS anticipates that any effects
from SAE’s seismic survey on marine
mammals, especially harbor seals and
Cook Inlet beluga whales, which are or
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have been taken for subsistence uses,
will be short-term, site specific, and
limited to inconsequential changes in
behavior and mild stress responses.
NMFS does not anticipate that the
authorized taking of affected species or
stocks will reduce the availability of the
species to a level insufficient for a
harvest to meet subsistence needs by: (1)
Causing the marine mammals to
abandon or avoid hunting areas; (2)
directly displacing subsistence users; or
(3) placing physical barriers between the
marine mammals and the subsistence
hunters; and that cannot be sufficiently
mitigated by other measures to increase
the availability of marine mammals to
allow subsistence needs to be met.
Based on the description of the
specified activity, the measures
described to minimize adverse effects
on the availability of marine mammals
for subsistence purposes, and the
required mitigation and monitoring
measures, NMFS has determined that
there will not be an unmitigable adverse
impact on subsistence uses from SAE’s
activities.
Endangered Species Act (ESA)
There are three marine mammal
species listed as endangered under the
ESA with confirmed or possible
occurrence in the project area: The Cook
Inlet beluga whale, the western DPS of
Steller sea lion, and the Central North
Pacific humpback whale. In addition,
the action could occur within 10 miles
of designated critical habitat for the
Cook Inlet beluga whale. NMFS’s
Permits and Conservation Division has
initiated consultation with NMFS’
Alaska Region Protected Resources
Division under section 7 of the ESA.
This consultation concluded on May 7,
2015, when a Biological Opinion was
issued. The Biological Opinion
determined that the issuance of an IHA
is not likely to jeapordize the continued
existence of the Cook Inlet beluga
whales, Central North Pacific humpback
whales, or western distinct population
segment of Steller sea lions or destroy
or adversely modify Cook Inlet beluga
whale critical habitat. Finally, the
Alaska region issued an Incidental Take
Statement (ITS) for Cook Inlet beluga
whales, humpback whales, and Steller
sea lions. The ITS contains reasonable
and prudent measures implemented by
the terms and conditions to minimize
the effect of this take.
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National Environmental Policy Act
(NEPA)
tkelley on DSK3SPTVN1PROD with NOTICES2
NMFS prepared an EA that includes
an analysis of potential environmental
effects associated with NMFS’ issuance
of an IHA to SAE to take marine
mammals incidental to conducting a 3D
seismic survey program in Cook Inlet,
Alaska. NMFS has finalized the EA and
prepared a FONSI for this action.
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Therefore, preparation of an
Environmental Impact Statement is not
necessary.
Authorization
As a result of these determinations,
NMFS has issued an IHA to SAE for the
take of marine mammals incidental to
conducting a seismic survey program in
Cook Inlet, Alaska, from May 13, 2015
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29189
through May 12, 2016, provided the
previously mentioned mitigation,
monitoring, and reporting requirements
are incorporated.
Dated: May 12, 2015.
Donna S. Wieting,
Director, Office of Protected Resources,
National Marine Fisheries Service.
[FR Doc. 2015–12091 Filed 5–19–15; 8:45 am]
BILLING CODE 3510–22–P
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Agencies
[Federal Register Volume 80, Number 97 (Wednesday, May 20, 2015)]
[Notices]
[Pages 29161-29189]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-12091]
[[Page 29161]]
Vol. 80
Wednesday,
No. 97
May 20, 2015
Part II
Department of Commerce
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National Oceanic and Atmospheric Administration
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Takes of Marine Mammals Incidental to Specified Activities; Taking
Marine Mammals Incidental to Seismic Surveys in Cook Inlet, Alaska;
Notices
Federal Register / Vol. 80 , No. 97 / Wednesday, May 20, 2015 /
Notices
[[Page 29162]]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XD830
Takes of Marine Mammals Incidental to Specified Activities;
Taking Marine Mammals Incidental to Seismic Surveys in Cook Inlet,
Alaska
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; issuance of an incidental harassment authorization.
-----------------------------------------------------------------------
SUMMARY: NMFS is issuing an Incidental Harassment Authorization in
response to a request from SAExploration Inc. (SAE) for authorization
to take marine mammals incidental to an oil and gas exploration seismic
survey program in Cook Inlet, Alaska between May 13, 2015 and May 12,
2016.
DATES: Effective: May 13, 2015 through May 12, 2016.
ADDRESSES: Electronic copies of the IHA, application, and associated
Environmental Assessment (EA) and Finding of No Significant Impact
(FONSI) may be obtained by writing to Jolie Harrison, Division Chief,
Permits and Conservation Division, Office of Protected Resources,
National Marine Fisheries Service, 1315 East West Highway, Silver
Spring, MD 20910, telephoning the contact listed below (see FOR FURTHER
INFORMATION CONTACT), or visiting the internet at: 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: Sara Young, 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 to allow, upon request, the
incidental, but not intentional, taking of small numbers of marine
mammals by U.S. citizens who engage in a specified activity (other than
commercial fishing) within a specified geographical region if certain
findings are made and either regulations are issued or, if the taking
is limited to harassment, a notice of a proposed authorization is
provided to the public for review.
An authorization for incidental takings shall be granted if NMFS
finds that the taking will have a negligible impact on the species or
stock(s), will not have an unmitigable adverse impact on the
availability of the species or stock(s) for subsistence uses (where
relevant), and if the permissible methods of taking and requirements
pertaining to the mitigation, monitoring and reporting of such takings
are set forth. NMFS has defined ``negligible impact'' in 50 CFR 216.103
as ``an impact resulting from the specified activity that cannot be
reasonably expected to, and is not reasonably likely to, adversely
affect the species or stock through effects on annual rates of
recruitment or survival.''
Except with respect to certain activities not pertinent here, the
MMPA defines ``harassment'' as: Any act of pursuit, torment, or
annoyance which (i) has the potential to injure a marine mammal or
marine mammal stock in the wild [Level A harassment]; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment].
Summary of Request
On October 28, 2014, we received a request from SAE for
authorization to take marine mammals incidental to seismic surveys in
Cook Inlet, Alaska. After further correspondence and revisions by the
applicant, we determined that the application was adequate and complete
on January 12, 2015. On March 20, 2015, NMFS published a notice in the
Federal Register of our proposal to issue an IHA with preliminary
determinations (80 FR 14913). The filing of the notice initiated a 30-
day public comment period. The comments and our responses are discussed
later in this document.
SAE proposes to conduct oil and gas exploration seismic surveys.
The activity will occur between May 13, 2015 and May 12, 2016, for a
period of 160 days. The following specific aspects of the activity are
likely to result in the take of marine mammals: Operation of seismic
airguns in arrays of 440 in\3\ and 1,760 in\3\. Take, by Level B
Harassment only, of individuals of beluga whale, humpback whale, minke
whale, gray whale, harbor porpoise, Dall's porpoise, killer whale,
harbor seal, and Steller sea lion is anticipated to result from the
specified activity.
Description of the Specified Activity
Overview
SAE plans to conduct 3D seismic surveys over multiple years in the
marine waters of both upper and lower Cook Inlet. This authorization
will cover activities occurring between May 13, 2015 and May 12, 2016.
The ultimate survey area is divided into two units (upper and lower
Cook Inlet). The total potential survey area is 3,934 square kilometers
(1,519 square miles); however, only a portion (currently unspecified)
of this area will ultimately be surveyed, and no more than 777 square
kilometers (300 square miles) in a given year. The exact location of
where the 2015 survey will be conducted is not known at this time, and
probably will not be known until late spring 2015 when SAE's clients
have finalized their data acquisition needs.
The components of the project include laying recording sensors
(nodes) on the ocean floor, operating seismic source vessels towing
active air gun arrays, and retrieval of nodes. There will also be
additional boat activity associated with crew transfer, recording
support, and additional monitoring for marine mammals. The primary
seismic source for offshore recording consists of a 2 x 880-cubic-inch
tri-cluster array for a total of 1,760-cubic-inches (although a 440-
cubic-inch array may be used in very shallow water locations as
necessary). Each of the arrays will be deployed in a configuration
outlined in Appendix A of the application. The arrays will be centered
approximately 15 meters (50 feet) behind the source vessel stern, at a
depth of 4 meters (12 feet), and towed along predetermined source lines
at speeds between 7.4 and 9.3 kilometers per hour (4 and 5 knots). Two
vessels with full arrays will be operating simultaneously in an
alternating shot mode; one vessel shooting while the other is
recharging. Shot intervals are expected to be about 16 seconds for each
array resulting in an overall shot interval of 8 seconds considering
the two alternating arrays. Operations are expected to occur 24 hours a
day, with actual daily shooting to total about 12 hours. An acoustical
positioning (or pinger) system will be used to position and interpolate
the location of the nodes. A vessel-mounted transceiver calculates the
position of the nodes by measuring the range and bearing from the
transceiver to a small acoustic transponder fitted to every third node.
The transceiver uses sonar to interrogate the transponders, which
respond with short pulses that are used in measuring the range and
bearing.
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Several offshore vessels will be required to support recording,
shooting, and housing in the marine and transition zone environments.
Exact vessels to be used have not been determined.
Dates and Duration
The request for incidental harassment authorization is primarily
for the 2015 Cook Inlet open water season. The plan is to conduct
seismic surveys in the Upper Cook unit sometime between May 13, 2015
through May 12, 2016. The northern border of the seismic survey area
depicted in Figure 1 takes into account the restriction that no
activity occur between April 15 to October 15 in waters within 16
kilometers (10 miles) of the Susitna Delta (defined as the nearshore
area between the mouths of the Beluga and the Little Susitna rivers). A
small wedge of the upper Cook unit falls within 16 kilometers of the
Beluga River mouth, but survey here will occur after October 15, taking
into account any timing restrictions with nearshore beluga habitat. The
seismic acquisition in lower Cook unit will initially begin in late
August or mid-September, and run until December 15 taking into account
any self-imposed location/timing restrictions to avoid encounters with
sea otters or Steller's eiders. The exact survey dates in a given unit
will depend on ice conditions, timing restrictions, and other factors.
If the upper Cook Inlet seismic surveys are delayed by spring ice
conditions, some survey may occur in lower Cook Inlet from March to May
to maximize use of the seismic fleet. Actual data acquisition is
expected to occur for only 2 to 3 hours at a time during each of the 3
to 4 daily slack tides. Thus, it is expected that the air guns will
operate an average of about 8 to 10 total hours per day. It is
estimated that it will take 160 days to complete both the upper and
lower Cook units, and that no more than 777 square kilometers (300
square miles) of survey area will be shot in 2015.
Specified Geographic Region
The area of Cook Inlet that SAE plans to operate in has been
divided into two subsections: Upper and Lower Cook Inlet. Upper Cook
(2,126 square kilometers; 821 square miles) begins at the line
delineating Cook Inlet beluga whale (Delphinapterus leucas) Critical
Habitat Area 1 and 2, south to a line approximately 10 kilometers (6
miles) south of both the Lower Cook (1,808 square kilometer; 698 square
mile) begins east of Kalgin Island and running along the east side of
lower Cook Inlet to Anchor Point (Figure 2 in SAE application).
Detailed Description of Activities
The Notice of Proposed IHA (80 FR 14913, March 20, 2015) contains a
full detailed description of the 3D seismic survey, including the
recording system, sensor positioning, and seismic source. That
information has not changed and is therefore not repeated here.
Comments and Responses
A Notice of Proposed IHA was published in the Federal Register on
March 20, 2015 (80 FR 14913) for public comment. During the 30-day
public comment period, NMFS received four comment letters from the
following: The Natural Resource Defense Council (NRDC); the Marine
Mammal Commission (MMC); Furie Operating Alaska LLC (Furie); and one
private citizen.
All of the public comment letters received on the Notice of
Proposed IHA (80 FR 14913, March 20, 2015) are available on the
internet at: https://www.nmfs.noaa.gov/pr/permits/incidental.htm.
Following is a summary of the public comments and NMFS' responses.
Comment 1: One private citizen requested that we deny issuance of
the IHA because marine mammals would be killed as a result of the
survey.
Response: Extensive analysis of the proposed 3D seismic survey was
conducted in accordance with the MMPA, Endangered Species Act (ESA),
and National Environmental Policy Act (NEPA). Pursuant to those
statutes, we analyzed the impacts to marine mammals (including those
listed as threatened or endangered under the ESA), their habitat
(including critical habitat designated under the ESA), and to the
availability of marine mammals for taking for subsistence uses. The
MMPA analyses revealed that the activities would have a negligible
impact on affected marine mammal species or stocks and would not have
an unmitigable adverse impact on the availability of marine mammals for
taking for subsistence uses. The ESA analysis concluded that the
activities likely would not jeopardize the continued existence of ESA-
listed species or destroy or adversely modify designated critical
habitat. The NEPA analysis concluded that there would not be a
significant impact on the human environment. Moreover, this activity is
not expected to result in the death of any marine mammal species, and
no such take is authorized.
Comment 2: Furie supports issuance of this IHA in a timely manner
and urge NMFS to recognize the benefits of seismic surveys and
subsequent development of energy resources.
Response: After careful evaluation of all comments and the data and
information available regarding potential impacts to marine mammals and
their habitat and to the availability of marine mammals for subsistence
uses, NMFS has issued the final authorization to SAE to take marine
mammals incidental to conducting a 3D seismic survey program in Cook
Inlet for the period May 13, 2015 through May 12, 2016.
Comment 3: The MMC recommends that NMFS defer issuance of the IHA
until such time as NMFS can, with reasonable confidence, support a
conclusion that the activities would affect no more than a small number
of Cook Inlet beluga whales and have no more than a negligible impact
on the population. The MMC recommends that NMFS defer issuance until we
have better information on the cause or causes of ongoing decline of
the population and a reasonable basis for determining that authorizing
additional takes would not contribute to or exacerbate that decline.
The MMC continues to believe that any activity that may contribute to
or that may worsen the observed decline should not be viewed as having
a negligible impact on the population. The NRDC states that NMFS failed
to meet both the ``small numbers'' and ``negligible impact'' standards.
Response: In accordance with our implementing regulations at 50 CFR
216.104(c), we use the best available scientific evidence to determine
whether the taking by the specified activity within the specified
geographic region will have a negligible impact on the species or stock
and will not have an unmitigable adverse impact on the availability of
such species or stock for subsistence uses. Based on the scientific
evidence available, NMFS determined that the impacts of the 3D seismic
survey program, which are primarily acoustic in nature, would meet
these standards. Moreover, SAE proposed and NMFS has required in the
IHA a rigorous mitigation plan to reduce impacts to Cook Inlet beluga
whales and other marine mammals to the lowest level practicable,
including measures to power down or shutdown airguns if any beluga
whale is observed approaching or within the Level B harassment zone and
restricting activities within a 10 mi (16 km) radius of the Susitna
Delta from April 15 through October 15, which is an important area for
beluga feeding and calving in the spring and summer months. This
shutdown measure is more restrictive than the standard shutdown
measures typically applied, and combined with the Susitna Delta
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exclusion (minimizing adverse effects to foraging), is expected to
reduce both the scope and severity of potential harassment takes,
ensuring that there are no energetic impacts from the harassment that
would adversely affect reproductive rates or survivorship.
Our analysis indicates that issuance of this IHA will not
contribute to or worsen the observed decline of the Cook Inlet beluga
whale population. Additionally, the ESA Biological Opinion determined
that the issuance of an IHA is not likely to jeopardize the continued
existence of the Cook Inlet beluga whales or the western distinct
population segment of Steller sea lions or destroy or adversely modify
Cook Inlet beluga whale critical habitat. The Biological Opinion also
outlined Terms and Conditions and Reasonable and Prudent Measures to
reduce impacts, which have been incorporated into the IHA. Therefore,
based on the analysis of potential effects, the parameters of the
seismic survey, and the rigorous mitigation and monitoring program,
NMFS determined that the activity would have a negligible impact on the
population.
Moreover, the seismic survey would take only small numbers of
marine mammals relative to their population sizes. The number of
belugas likely to be taken represent less than 9.6% of the population.
As described in the proposed IHA Federal Register notice, NMFS used a
method that incorporates density of marine mammals overlaid with the
anticipated ensonified area to calculate an estimated number of takes
for belugas, which was estimated to be less than 10% of the stock
abundance, which NMFS considers small. In addition to this quantitative
evaluation, NMFS has also considered qualitative factors that further
support the ``small numbers'' determination, including: (1) The
seasonal distribution and habitat use patterns of Cook Inlet beluga
whales, which suggest that for much of the time only a small portion of
the population would be accessible to impacts from SAE's activity, as
most animals are concentrated in upper Cook Inlet; and (2) the
mitigation requirements, which provide spatio-temporal limitations that
avoid impacts to large numbers of animals feeding and calving in the
Susitna Delta and limit exposures to sound levels associated with Level
B harassment. Based on all of this information, NMFS determined that
the number of beluga whales likely to be taken is small. See response
to Comment 5 and our small numbers analysis later in this document for
more information about the small numbers determination for beluga
whales and the other marine mammal species.
Comment 4: The MMC recommends that NMFS develop a policy that sets
forth clear criteria and/or thresholds for determining what constitutes
``small numbers'' and ``negligible impact'' for the purpose of
authorizing incidental takes of marine mammals. The MMC understands
that NMFS has been working on developing a policy and would welcome an
opportunity to discuss this policy further before it is finalized.
Response: NMFS is in the process of developing both a clearer
policy to outline the criteria for determining what constitutes ``small
numbers'' and an improved analytical framework for determining whether
an activity will have a ``negligible impact'' for the purpose of
authorizing takes of marine mammals. We fully intend to engage the MMC
in these processes at the appropriate time.
Comment 5: The NRDC pointed by reference to the other proposed
activities in Cook Inlet during the 2015 open water season. The NRDC
and the MMC both note that NMFS must address the cumulative effects of
activities in Cook Inlet on Cook Inlet beluga whales and whether the
cumulative impacts of all the activities are having ``either
individually or in combination'' a greater than negligible impact on
marine mammals.
Response: Neither the MMPA nor NMFS' implementing regulations
specify how to consider other activities and their impacts on the same
populations when conducting a negligible impact analysis. However,
consistent with the 1989 preamble for NMFS' implementing regulations
(54 FR 40338, September 29, 1989), the impacts from other past and
ongoing anthropogenic activities are incorporated into the negligible
impact analysis via their impacts on the environmental baseline (e.g.,
as reflected in the density/distribution and status of the species,
population size and growth rate, and ambient noise).
In addition, cumulative effects were addressed in the EA and
Biological Opinion prepared for this action. The cumulative effects
section of the EA has been expanded from the draft EA to discuss
potential effects in greater detail. These documents, as well as the
Alaska Marine Stock Assessments and the most recent abundance estimate
for Cook Inlet beluga whales (Shelden et al., 2015, are part of NMFS'
Administrative Record for this action, and provided the decision maker
with information regarding other activities in the action area that
affect marine mammals, an analysis of cumulative impacts, and other
information relevant to the determination made under the MMPA.
Comment 6: The NRDC states that NMFS failed to account for survey
duration in the estimation of beluga whale takes and that NMFS based
beluga takes using a predictive habitat density model (Goetz et al.,
2012) that is based on data from summer months and confined to summer
distribution when belugas are generally concentrated in the Upper
Inlet, even though activity could occur year round.
Response: The numerical estimation of take for beluga whales does
consider survey duration in the calculation. The Goetz et al 2012 model
is the best available data for beluga density in Cook Inlet. The method
used by NMFS to estimate take uses the best available data to most
accurately estimate the number of belugas taken. This is done by
multiplying the density of the area surveyed on a given day by the area
ensonified on that day of surveying to yield the number of belugas that
were likely exposed during that day of surveying. This is then added to
the next day of surveying and so forth in an additive model until the
number of 30 belugas is reached. If the number of 30 belugas is reached
using this calculation before SAE has completed their 160 days of
proposed surveying, survey activity must cease. Additionally, if they
finish their 160 days without reaching the limit of 30 belugas their
activity must still cease. The model, by being additive in nature for
each day of surveying, accounts for the duration of the survey, as well
as capturing a more specific density value than using an Inlet-wide
density estimate.
Moreover, the model (or other numerical methods for estimating
take) does not take into consideration the rigorous mitigation
protocols that will be implemented by SAE to reduce the number of
actual Level B harassment takes of Cook Inlet beluga whales. As
mentioned previously, the IHA contains a condition restricting SAE's
airgun operations within 10 mi (16 km) of the mean higher high water
line of the Susitna Delta from April 15 through October 15. During this
time, a significant portion of the Cook Inlet beluga whale population
occurs in this area for feeding and calving. This setback distance
includes the entire 160 dB radius of 5.9 mi (9.5 km) predicted for the
full airgun array plus an additional 4.1 mi (6.5 km) of buffer, thus
reducing the number of animals that may be exposed to Level B
harassment thresholds. SAE is also required to shut down the airguns if
any beluga whale is
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sighted approaching or entering the Level B harassment zone to avoid
take. NMFS combined use of the National Marine Mammal Laboratory (NMML)
model, which we determined to be the best available data upon which to
base density estimates, with consideration of all of the mitigation
measures required to be implemented to authorize 30 beluga whale takes.
This approach is reasonable and does not contradict available science
and data of beluga whale distribution and local abundance during the
period of operations.
Comment 7: The NRDC states that in the case of marine mammals other
than beluga whales, NMFS repeated past errors associated with its use
of raw NMML survey data. Errors in the density calculations include the
failure to incorporate correction factors for missed marine mammals in
the analysis and the failure to fully account for survey duration by
multiplying densities (which are calculated on an hourly basis) by the
number of survey days but not the number of hours in a day.
Response: Correction factors for marine mammal surveys, with the
exception of beluga whales, are not available for Cook Inlet. The
primary purpose and focus of the NMFS aerial surveys in Cook Inlet for
the past decade has been to monitor the beluga whale population.
Although incidental observations of other marine mammals are noted
during these surveys, they are focused on beluga whales. With the
exception of the beluga whale, no detailed statistical analysis of Cook
Inlet marine mammal survey results has been conducted, and no
correction factors have been developed for Cook Inlet marine mammals.
The only published Cook Inlet correction factor is for beluga whales.
Developing correction factors for other marine mammals would have
required different survey data collection and consideration of
unavailable data such as Cook Inlet sight ability, movement patterns,
tidal correlations and detailed statistical analyses. For example,
other marine mammal numbers are often rounded to the nearest 10 or 100
during the NMFS aerial survey; resulting in unknown observation bias.
Therefore, the data from the NMFS surveys are the best available and
number of animals taken are still likely overestimated because of the
assumption that there is a 100% turnover rate of marine mammals each
day.
Survey duration was appropriately considered in the estimations by
multiplying density by area of ensonification by number of survey days.
NMFS does not calculate takes on an hourly basis, and, additionally,
the multiple hours surveyed within a day are reflected in the area of
ensonification, which considers the distance they can move within a day
and is therefore larger than what would be covered in one hour.
Additionally, as NMFS has used the density estimate from NMFS aerial
surveys, multiplied by the area ensonified per day, multiplied by the
number of days, this calculation produces the number instances of
exposure during the survey. This is likely an overestimate of
individuals taken by Level B harassment, as a single individual can be
exposed on multiple days over the course of the survey, especially when
a small patch of area is shot over a duration of five days. While
protected species observers (PSOs) cannot detect every single animal
within the Level B harassment zone, monitoring reports from similar
activities indicate that sightings did not exceed anticipated
estimates.
Comment 8: The NRDC commented that NMFS underestimated the size of
SAE's impact area by: (1) Using an outdated and incorrect threshold for
behavioral take; and (2) disregarding the best available evidence on
the potential for temporary and permanent threshold shift on mid- and
high-frequency cetaceans and on pinnipeds.
Response: The comment that NMFS uses an outdated and incorrect
threshold for behavioral takes does not include any specific
recommendations. NMFS uses 160 dB (rms) as the exposure level for
estimating Level B harassment takes for most species in most cases.
This threshold was established for underwater impulse sound sources
based on measured avoidance responses observed in whales in the wild.
Specifically, the 160 dB threshold was derived from data for mother-
calf pairs of migrating gray whales (Malme et al., 1983, 1984) and
bowhead whales (Richardson et al., 1985, 1986) responding to seismic
airguns (e.g., impulsive sound source). We acknowledge there is more
recent information bearing on behavioral reactions to seismic airguns,
but those data only illustrate how complex and context-dependent the
relationship is between the two. See 75 FR 49710, 49716 (August 13,
2010) (IHA for Shell seismic survey in Alaska). Accordingly, it is not
a matter of merely replacing the existing threshold with a new one.
NOAA is working to develop more sophisticated draft guidance for
determining impacts from acoustic sources, including information for
determining Level B harassment thresholds. Due to the complexity of the
task, any guidance will require a rigorous review that includes
internal agency review, public notice and comment, and additional
external peer review before any final product is published. In the
meantime, and taking into consideration the facts and available
science, NMFS determined it is reasonable to use the 160 dB threshold
for estimating takes of marine mammals in Cook Inlet by Level B
harassment. However, we discuss the science on this issue qualitatively
in our analysis of potential effects to marine mammals.
The comment that NMFS disregarded the best available evidence on
the potential for temporary and permanent threshold shift on mid- and
high-frequency cetaceans and on pinnipeds does not contain any specific
recommendations. We acknowledge there is more recent information
available bearing on the relevant exposure levels for assessing
temporary and permanent hearing impacts. (See NMFS' Federal Register
notice (78 FR 78822, December 27, 2013) for NMFS' draft guidance for
assessing the onset of permanent and temporary threshold shift.) Again,
NMFS will be issuing guidance, but that process is not complete, so we
did not use it to assign new thresholds for calculating take estimates
for hearing impacts. However, we did consider the information, and it
suggests the current 180 and 190 dB thresholds are appropriate and that
they likely overestimate potential for hearing impacts. See 75 FR
49710, 49715, 49724 (August 13, 2010) (IHA for Shell seismic survey in
Alaska; responses to comment 8 and comment 27). Moreover, the required
mitigation is designed to ensure there are no exposures at levels
thought to cause hearing impairment, and, for several of the marine
mammal species in the project area, mitigation measures are designed to
reduce or eliminate exposure to Level B harassment thresholds.
Comment 9: The NRDC comments that the proposed mitigation measures
fail to meet the MMPA's ``least practicable adverse impact'' standard.
The NRDC provides a list of approximately eight measures that NMFS
``failed to consider or adequately consider.''
Response: NMFS provided a detailed discussion of proposed
mitigation measures and the MMPA's ``least practicable impact''
standard in the notice of the proposed IHA (80 FR 14913, March 20,
2015), which are repeated in the ``Mitigation'' section of this notice.
The measures that NMFS allegedly failed to consider or
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adequately consider are identified and discussed below:
(1) Field testing and use of alternative technologies, such as
vibroseis and gravity gradiometry, to reduce or eliminate the need for
airguns and delaying seismic acquisition in higher density areas until
the alternative technology of marine vibroseis becomes available: SAE
requested takes of marine mammals incidental to the seismic survey
operations described in the IHA application, which identified airgun
arrays as the technique SAE would employ to acquire seismic data. It
would be inappropriate for NMFS to change the specified activity and it
is beyond the scope of the request for takes incidental to SAE's
operation of airguns and other active acoustic sources.
SAE knows of no current technology scaled for industrial use that
is reliable enough to meet the environmental challenges of operating in
Cook Inlet. SAE is aware that many prototypes are currently in
development, and may ultimately incorporate these new technologies into
their evaluation process as they enter commercial viability. However,
none of these technologies are currently ready for use on a large scale
in Cook Inlet. As this technology is developed, SAE will evaluate its
utility for operations in the Cook Inlet environment.
(2) Required use of the lowest practicable source level in
conducting airgun activity: SAE determined that the 1760 in\3\ array
provides the data required for SAE's operations.
(3) Seasonal exclusions around river mouths, including early spring
(pre-April 14) exclusions around the Beluga River and Susitna Delta,
and avoidance of other areas that have a higher probability of beluga
occurrence: NMFS has required a 10 mile (16 km) exclusion zone around
the Susitna Delta (which includes the Beluga River) in this IHA. This
mitigation mirrors a measure in the Incidental Take Statement for the
2012 and 2013 Biological Opinions. Seismic survey operations involving
the use of airguns will be prohibited in this area between April 15 and
October 15. In both the MMPA and ESA analysis, NMFS determined that
this date range is sufficient to protect Cook Inlet beluga whales and
the critical habitat in the Susitna Delta. While data indicate that
belugas may use this part of the inlet year round, peak use occurs from
early May to late September. NMFS added a 2-week buffer on both ends of
this peak usage period to add extra protection to feeding and calving
belugas. (In addition, the Alaska Department of Fish and Game (ADF&G)
prohibits the use of airguns within 1 mi (1.6 km) of the mouth of any
stream listed by the ADF&G on the Catalogue of Waters Important for the
Spawning, Rearing, or Migration of Anadromous Fishes. See additional
explanation in ``Mitigation Measures Considered but not Required''
section, later in this document.)
(4) Limitation of the mitigation airgun to the longest shot
interval necessary to carry out its intended purpose: This general
comment contained no specific recommendations. SAE requires shot
intervals of 50m at a speed of 4-5 knots to obtain the information from
their survey. However NMFS has added a mitigation measure that SAE
reduce the shot interval for the mitigation gun to one shot per minute.
(5) Immediate suspension of airgun activity, pending investigation,
if any beluga strandings occur within or within an appropriate distance
of the survey area. The IHA requires SAE to immediately cease
activities and report unauthorized takes of marine mammals, such as
live stranding, injury, serious injury, or mortality. NMFS will review
the circumstances of SAE's unauthorized take and determine if
additional mitigation measures are needed before activities can resume
to minimize the likelihood of further unauthorized take and to ensure
MMPA compliance. SAE may not resume activities until notified by NMFS.
Separately the IHA includes measures if injured or dead marine mammals
are sighted and the cause cannot be easily determined. In those cases,
NMFS will review the circumstances of the stranding event while SAE
continues with operations.
(6) Establishment of a larger exclusion zone for beluga whales that
is not predicated on the detection of whale aggregations or cow-calf
pairs: Both the proposed IHA notice and the issued IHA contain a
requirement for SAE to delay the start of airgun use or shutdown the
airguns if a beluga whale is visually sighted or detected by passive
acoustic monitoring approaching or within the 160-dB disturbance zone
until the animal(s) are no longer present within the 160-dB zone. The
measure applies to the sighting of any beluga whale, not just sightings
of groups or cow-calf pairs.
Comment 10: The MMC suggests additional mitigation measures are
used including: (1) Aerial surveys, (2) passive acoustic monitoring, as
well as (3) a 30 minute post-activity monitoring period.
Response: NMFS provided a detailed discussion of proposed
mitigation measures and the MMPA's ``least practicable impact''
standard in the notice of the proposed IHA (80 FR 14913, March 20,
2015), which are repeated in the ``Mitigation'' section of this notice.
The measures that NMFS allegedly failed to consider or adequately
consider are identified and discussed below:
(1) Use of advance aerial surveys to redirect activity is not
required for this action. Aerial surveys for this project could be used
for monitoring the disturbance zone to the 160dB level (6.83 km).
However, exposures that occur in this zone, or Level B takes, are
already accounted for in the take estimation section below. Visual
observers, which are already known to be effective in this environment,
will adhere to strict standards for preventing animals from entering
the 180dB/190dB injury exclusion zone, as well as monitoring for
animals that may be traveling in the direction of or approaching the
injury exclusion zone. The prohibitive cost of daily aerial surveys for
a survey area of only 777km\2\, combined with the limited added value
given the general effectiveness of vessel and land-based observers, and
considering the fact that we believe that the activity will have a
negligible impact even in the absence of mitigation make the suite of
mitigation measures we have included adequate to achieve the least
practicable adverse impact.
(2) The passive acoustic monitoring plan for Apache Alaska
Corporation's 2012 survey anticipated the use of a bottom-mounted
telemetry buoy to broadcast acoustic measurements using a radio-system
link back to a monitoring vessel. Although a buoy was deployed during
the first week of surveying under the 2012 IHA, it was not successful.
Upon deployment, the buoy immediately turned upside down due to the
strong current in Cook Inlet. After retrieval, the buoy was not
redeployed and the survey used a single omni-directional hydrophone
lowered from the side of the mitigation vessel. During the entire 2012
survey season, Apache's PAM equipment yielded only six confirmed marine
mammal detections, one of which was a Cook Inlet beluga whale. The
single Cook Inlet beluga whale detection did not, however, result in a
shutdown procedure.
Additionally, Joint Base Elmendorf-Fort Richardson, the National
Marine Mammal Laboratory, and Alaska Department of Fish & Game
conducted a 2012 study (Gillespie et al., 2013) to determine if beluga
whale observations at the mouth of Eagle River corresponded with
acoustic detections received by a PAMBuoy data collection system. The
PAMBuoy data collection system was deployed in the mouth of
[[Page 29167]]
Eagle River from 12-31 August 2012. This study was a trial period
conducted with one hydrophone at the mouth of the river. Overall, it
was successful in detecting beluga whale echolocation clicks and
whistles, but came with several limitations:
The PAM system was able to reliably detect all whales
approaching or entering the river but still performs less well than a
human observer;
Sounds from vessels in Cook Inlet (e.g. vessel noise) have
a large chance of interfering with detections from PAM. The mouth of
Eagle River has very little vessel traffic, which is likely why the
study was successful there and not likely to be successful in Cook
Inlet;
PAMbouys could be a navigational hazard in Cook Inlet for
commercial, subsistence, and sport fishing, as well as the commercial
vessel traffic traveling through Cook Inlet;
The limited testing in a very small area should not become
the new standard of monitoring in the entire Cook Inlet. The tide,
vessel traffic, bathymetry, and substrate of Cook Inlet are far more
complex than the study area;
It appears the hydrophone must be hardwired to the shore
which is not practical for mobile marine seismic operations;
Currently, deployment of the system is done by walking
tripods onto the mudflats. This is not feasible for the vast majority
of the SAE project area. Walking onto the mudflats in parts of Cook
Inlet also poses a safety risk;
The study found considerable investment would be necessary
to develop an ice and debris proof mounting system. Other issues with
hydrophone configuration include: At extreme low tides, the hydrophone
was uncovered and therefore not usable; the hydrophone had to be
located in such a position so that it could be occasionally visually
inspected; hydrophone battery supply has to constantly be checked; the
costs and practicalities of long-term hydrophone mounting and data
transmission have not been determined.; and only one hydrophone was
tested, and SAE would need several hydrophones;
Observer sightings and acoustic detections of belugas
generally corresponded with one another. Thus PAMBuoys would be simply
duplicating PSO and aerial efforts;
The wireless modem that transmits the acoustic data to the
``base station'' was only tested to 3.2 km; and
The study did not conclude anything about the detection
range of the system, except that it was greater than 400 m.
NMFS has been made aware of an over-the-side hydrophone that has
successfully detected belugas in Eagle River, Alaska. Upon beginning
operations, SAE has 30 days to acquire a hydrophone that covers a
frequency range of 0.1-160 kHz to allow detecting both social and
echolocation signals, with a system sensitivity in the range -165 to -
185 dB re1 V/[mu]Pa, and floor noise spectra similar to Beaufort Sea
State 0. SAE will use this hydrophone during nighttime ramp-ups from
the mitigation airgun to detect beluga whales, humpbacks, and Steller
sea lions that may be within the 160dB disturbance zone.
(3) A post-activity monitoring period of 30 minutes has been added
as a requirement for this activity. This monitoring period after the
cessation of airgun operations can provide useful observations to
compare the behavior and abundance of animals during different
scenarios of various noise levels. This change has been noted in the
Authorization text.
Comment 11: The MMC notes that NMFS is reviewing two other IHA
applications for proposed seismic surveys in Cook Inlet in 2015 and
that it is not clear whether these applications are seeking separate
authorizations for some or all of the same activities. NMFS needs to
adopt policies and institute procedures to ensure that separate
applications to conduct essentially the same activities in the same
areas are considered more holistically. If indeed the applicants are
proposing to conduct multiple seismic surveys within the same area, it
would increase the numbers of marine mammals taken and expose beluga
whales and other marine mammals to unnecessary, avoidable risks.
Section 101(a)(5)(D)(ii)(I) of the MMPA directs NMFS to structure IHAs
so that they prescribe ``other means of effecting the least practicable
impact on such species or stock and its habitat.'' Allowing multiple
operators to obtain separate IHAs to conduct duplicative surveys is
inconsistent with that mandate. Data sharing and collaboration is
critical in habitat areas used by endangered populations, such as Cook
Inlet beluga whales. The MMC recommends that NMFS encourage SAE and
other applicants proposing to conduct seismic surveys in Cook Inlet in
2015 to collaborate on those surveys and, to the extent possible,
submit a single application seeking authorization for incidental
harassment of marine mammals.
In a similar comment, the NRDC expressed concern over the number of
activities proposed in the same area for the same season referencing
applications for: Furie, Bluecrest, Buccaneer, and Apache.
Response: We agree and have encouraged SAE to cooperate with other
interested parties to minimize the impacts of new seismic surveys in
the region. Apache has told NMFS that their proposed activities are a
separate project to that of SAE. Currently, SAE works with other oil
and gas operators in the area to enter into cooperative agreements.
Sometimes these negotiations are successful, but at other times the
companies cannot reach an agreement acceptable to both parties. SAE
will continue its discussions with other operators in Cook Inlet to
find opportunities to joint venture in oil and gas operations,
including seismic data acquisition.
The portion of the statute cited by the MMC refers to the need to
require mitigation measures to ensure that the specified activity for
which take is authorized in that particular authorization ``effects the
least practicable impact.'' SAE proposed and NMFS has required a
rigorous mitigation and monitoring plan to ensure that SAE's program
meets that standard. Moreover, NMFS will not issue IHAs to other
applicants if the negligible impact standard cannot be met.
Lastly, there are no applications being processed for Furie or
Buccaneer. Apache does not anticipate conducting seismic activity in
the 2015 season. Additionally, the activities proposed by Bluecrest are
not seismic surveys and in a far southerly portion of the Inlet, with
no overlap with SAE's activities.
Comment 12: Both the NRDC and the MMC comment that authorization
should not be issued until the Cook Inlet Beluga Whale Take Recovery
Plan is finalized and published.
Response: The Cook Inlet Beluga Whale Recovery Plan is still under
development and will not be available in time to authorize activities
for the 2015 open water season. It is possible the Recovery Plan will
be available for next season. It is not necessary to have the Recovery
Plan finalized to authorize SAE's activity, as NMFS is still able to
make a negligible impact determination for beluga whales.
Comment 13: The MMC comments that various applicants in the Cook
Inlet region have used differing density estimates for calculating take
of marine mammal species in the Inlet and that all applicants should
use the same densities.
Response: The density estimates used by SAE specifically for harbor
porpoises, harbor seals, and killer whales are the best available
science at
[[Page 29168]]
this time. The data are from NMFS aerial surveys over a ten year period
(2000-2012). NMFS is working with applicants to incorporate these
density estimates into future applications and take authorizations.
However, where applicable, density estimates and derived take
estimation may vary based on site-specific knowledge of abundance,
density, seasonality, or other qualities that could allow for a more
nuanced assessment of the presence of a particular stock in a given
location.
Comment 14: The MMC also comments that in the application, SAE
states it will only survey in an area of 777km\2\ but that the proposed
action area is much larger. The MMC requests that SAE specify the area
in which they expect to operate so that take estimations more
accurately reflect the scope of the project.
Response: Due to the nature of SAE's work, contracts are awarded
throughout the season and the exact locations of operation are not
known to SAE at the time of the application. However, SAE has provided
how much area they plan to survey and NMFS has calculated take
estimation using the number of survey days requested and daily
ensonified area to calculate take instead of the 777km\2\ unique area
specified in the application to ensure a robust calculation of
exposures to the 160dB level.
Comment 15: The MMC comments that SAE should be required to
investigate and report on detection probabilities from various
observation platforms for differing sea states and light conditions.
Response: NMFS acknowledges that collecting detection probabilities
from various platforms under different conditions would be very useful
information and could better inform monitoring reports by discerning
how many animals were likely taken. However, constructing a study to
investigate detection probabilities requires a great deal of planning
and many more observers than are involved in this survey. NMFS would
like to work with the MMC in the future to discuss how best to conduct
this work and refine detection probabilities for seismic surveys.
Comment 16: The NRDC comments on several issues under NEPA, related
to cumulative effects and the suite of alternatives. These comments
are: (1) NEPA mandates that NMFS may not authorize activities while a
programmatic EIS is underway; (2) The No Action alternative must assume
SAE will not conduct the proposed activity; and (3) The third
alternative with additional mitigation measures is not sufficiently
analyzed and defined.
Response: The NEPA analysis is an important component of our
process. Our responses to the issues raised by the NRDC are as follows:
(1) The regulatory text referenced by NRDC in their comments, 40
CFR 1506.1, states that ``While work on a required program
environmental impact statement is in progress and the action is not
covered by an existing program statement, agencies shall not undertake
in the interim any major Federal action covered by the program which
may significantly affect the quality of the human environment.'' NRDC
is likely referencing NMFS' Federal Register Notice of Intent to
Prepare an EIS for Cook Inlet (79 FR 61616; October 14, 2014). That
provision is not applicable here as NMFS' decision to prepare an EIS is
not required, but rather voluntary. The programmatic EIS is meant to
address hypothetical increasing future levels of activity in Cook
Inlet, not a specific proposed project. Lastly, the regulatory text
references activities that are expected to have a significant impact on
the human environment, and NMFS has determined that this activity will
not have such an impact, as specified in the Finding of No Significant
Impact (FONSI). At this time, NMFS is evaluating each activity
individually, taking into consideration cumulative impacts, with an EA,
to determine if the action under consideration can support a FONSI.
(2) The No Action alternative in NMFS' draft EA for this activity
was written to reflect a situation in which NMFS did not authorize the
activity and the survey went forward without mitigation and monitoring.
However, after further consideration, NMFS has decided to modify the No
Action alternative to represent a situation in which NMFS did not issue
an authorization and the applicant did not conduct their proposed
activity. These changes are reflected in the Final EA.
(3) The third alternative in the EA is a scenario that includes all
of the mitigation measures of the preferred alternative, as well as
additional cutting edge technologies that have been suggested by
commenters in previous authorizations, including NRDC. However, this
alternative does not contain the more detailed analysis requested by
NRDC because many of the included technologies are not viable at this
time. Many are still in the developmental or preliminary testing phase,
or do not currently have guidelines pertaining to appropriate operating
conditions around marine mammals, such as unmanned aerial vehicles. The
No Action alternative and the Preferred alternative both contain more
in-depth analyses as appropriate.
Comment 17: The NRDC comments that the dates in the proposed IHA
suggest a curtailing of public review in violation of the
Administrative Procedure Act.
Response: The date provided in the proposed IHA was the date
proposed by the applicant originally for this work. Due to the time
required to analyze and respond to comments sufficiently, this date was
postponed and the authorization will be effective on: May 13, 2015.
Comment 18: The MMC comments that the use of a 2.5 turnover factor
in take estimation of harbor seals is inappropriate. The MMC requests
that NMFS use the same density x daily ensonified area x number of days
formula used for the other species. The MMC also notes that if NMFS
uses a turnover factor that it should consult the literature to create
a more biologically relevant turnover factor than Wood et al. 2012.
Response: After reviewing the Commission's comment, NMFS decided to
adjust the method used to estimate take for harbor seals in Cook Inlet.
The daily ensonified area x number of survey days x density method
yields an estimate of instances of take that is 19,315. Not only is
this likely an overestimate of instances, but it is also significantly
higher than the number of individual harbor seals expected to be
exposed, as described in more details in the Estimated Take section.
NMFS applied the survey method used by SAE, patch shooting, and applied
the number of days required to shoot a patch to estimate the number of
days an animal at a given haulout could be exposed. This is an average
of 3 days, but no more than 5. When this factor is applied to the
overestimate of exposures by using the ensonified daily area method,
the number of exposed seals is much lower, at 6,438. This number may be
reduced even further as individuals could be exposed at multiple
patches. Separately, NMFS then considered the harbor seal densities
alongside monitoring reports from Apache's work in 2012. NMFS looked at
the monitoring reports from Apache's aerial surveys in June and used
correction factors from the literature to determine the number of seals
in the water. This number was also multiplied to match the number of
SAE's proposed survey days (160) to yield a number of 8,250 instances
of take, notably lower than 19,315. Additionally, in their 147 days of
surveying, Apache reported sightings of 285 seals. While it is
understood that
[[Page 29169]]
this is lower than the actual number of exposures, as all seals in the
160dB range are not visible, this number is 131 times smaller than the
calculated number of exposures using the daily ensonified area method.
These methods are discussed in greater detail in the Takes Estimation
section of this document, but in summary we concluded that not more
than 25% of the population of harbor seals would be taken.
Description of Marine Mammals in the Area of the Specified Activity
Marine mammals most likely to be found in the upper Cook activity
area are the beluga whale (Delphinapterus leucas), harbor porpoise
(Phocoena phocoena), and harbor seal (Phoca vitulina). However, these
species are found there in low numbers, and generally only during the
summer fish runs (Nemeth et al. 2007, Boveng et al. 2012). These
species are also found in the Lower Cook Inlet survey area along with
humpback whales (Megaptera novaeangliae), minke whales (Balaenoptera
acutorostra), gray whales (Eschrichtius robustus), killer whales
(Orcinus orca), Dall's porpoise (Phocoenoides dalli), and Steller sea
lions (Eumetopia jubatus). Minke whales have been considered migratory
in Alaska (Allen and Angliss, 2014) but have recently been observed off
Cape Starichkof and Anchor Point year-round (Owl Ridge, 2014). Humpback
and gray whales are seasonal in Lower Cook, while the remaining species
could be encountered at any time of the year. During marine mammal
monitoring conducted off Cape Starichkof between May and August 2013,
observers recorded small numbers of humpback whales, minke whales, gray
whales, killer whales, and Steller sea lions, and moderate numbers of
harbor porpoises and harbor seals (Owl Ridge, 2014). This survey also
recorded a single beluga observed 6 kilometers north of Cape Starichkof
in August 2013. The stock sizes for marine mammals found in the project
area in Cook Inlet are shown in Table 1.
Table 1--Marine Mammals Inhabiting the Cook Inlet Action Area
----------------------------------------------------------------------------------------------------------------
Stock abundance Relative
ESA/MMPA status (CV, Nmin, most occurrence in Cook
Species Stock \1\; Strategic (Y/ recent abundance Inlet; season of
N) survey) \2\ occurrence
----------------------------------------------------------------------------------------------------------------
Humpback whale................. Central North E/D;Y.............. 7,469 (0.095; Occasionally seen
Pacific. 5,833; 2000). in Lower Inlet,
summer.
Minke whale.................... Alaska............ -;N................ 1,233 (0.034; N/A; Infrequently occur
2003). but reported year-
round.
Gray whale..................... Eastern North -;N................ 19,126 (0.071; Rare migratory
Pacific. 18,017; 2007). visitor; late
winter.
Killer whale................... Alaska Resident... -;N................ 2,347 (N/A; 2,084; Occasionally
2009). sighted in Lowe
Cook Inlet.
Alaska Transient.. -:N................ 345 (N/A; 303;
2003).
Beluga whale................... Cook Inlet........ E/D;Y.............. 312 (0.10; 280; Use upper Inlet in
2012). summer and lower
in winter:
annual.
Harbor porpoise................ Gulf of Alaska.... -;Y................ 31,046 (0.214; Widespread in the
25,987; 1998). Inlet: annual
(less in winter).
Dall's porpoise................ Alaska............ ................... .................. Infrequently found
in Lower Inlet.
Steller sea lion............... Western DPS....... E/D;Y.............. 79,300 (N/A; Primarily found in
45,659; 2012). lower Inlet.
Harbor seal.................... Cook Inlet/ -;N................ 22,900 (0.053; Frequently found
Shelikof. 21,896; 2006). in upper and
lower inlet;
annual (more in
northern Inlet in
summer).
----------------------------------------------------------------------------------------------------------------
Source: Allen and Angliss (20142, 2013), Carretta et al. (2013), Zerbini et al. (2006)
Humpback Whale (Megaptera novaeangliae)
Although there is considerable distributional overlap in the
humpback whale stocks that use Alaska, the whales seasonally found in
lower Cook Inlet are probably of the Central North Pacific stock.
Listed as endangered under the Endangered Species Act (ESA), this stock
has recently been estimated at 7,469, with the portion of the stock
that feeds in the Gulf of Alaska estimated at 2,845 animals (Allen and
Angliss 2014). The Central North Pacific stock winters in Hawaii and
summers from British Columbia to the Aleutian Islands (Calambokidis et
al. 1997), including Cook Inlet.
Humpback use of Cook Inlet is largely confined to lower Cook Inlet.
They have been regularly seen near Kachemak Bay during the summer
months (Rugh et al. 2005a), and there is a whale-watching venture in
Homer capitalizing on this seasonal event. There are anecdotal
observations of humpback whales as far north as Anchor Point, with
recent summer observations extending to Cape Starichkof (Owl Ridge
2014). Humpbacks might be encountered in the vicinity of Anchor Point
if seismic operations were to occur off the point during the summer.
However, SAE plans, for the most part, to limit seismic activity along
the Kenai Peninsula to during the spring and fall.
Minke Whale (Balaenoptera acutorostra)
Minke whales are the smallest of the rorqual group of baleen whales
reaching lengths of up to 35 feet. They are also the most common of the
baleen whales, although there are no population estimates for the North
Pacific, although estimates have been made for some portions of Alaska.
Zerbini et al. (2006) estimated the coastal population between Kenai
Fjords and the Aleutian Islands at 1,233 animals.
During Cook Inlet-wide aerial surveys conducted from 1993 to 2004,
minke whales were encountered only twice (1998, 1999), both times off
Anchor Point 16 miles northwest of Homer. A minke whale was also
reported off Cape Starichkof in 2011 (A. Holmes, pers. comm.) and 2013
(E. Fernandez and C. Hesselbach, pers. comm.), suggesting this location
is regularly used by minke whales, including during the winter.
Recently, several minke whales were recorded off Cape Starichkof in
early summer 2013 during exploratory drilling conducted there (Owl
Ridge 2014). There are no records north of Cape Starichkof, and this
species is unlikely to be seen in upper Cook Inlet. There is a chance
of encountering this
[[Page 29170]]
whale during seismic operations along the Kenai Peninsula in lower Cook
Inlet.
Gray Whale (Eschrichtius robustus)
Each spring, the Eastern North Pacific stock of gray whale migrates
8,000 kilometers (5,000 miles) northward from breeding lagoons in Baja
California to feeding grounds in the Bering and Chukchi seas, reversing
their travel again in the fall (Rice and Wolman 1971). Their migration
route is for the most part coastal until they reach the feeding
grounds. A small portion of whales do not annually complete the full
circuit, as small numbers can be found in the summer feeding along the
Oregon, Washington, British Columbia, and Alaskan coasts (Rice et al.
1984, Moore et al. 2007).
Human exploitation reduced this stock to an estimated ``few
thousand'' animals (Jones and Schwartz 2002). However, by the late
1980s, the stock was appearing to reach carrying capacity and estimated
to be at 26,600 animals (Jones and Schwartz 2002). By 2002, that stock
had been reduced to about 16,000 animals, especially following
unusually high mortality events in 1999 and 2000 (Allen and Angliss
2014). The stock has continued to grow since then and is currently
estimated at 19,126 animals with a minimum estimate of 18,017 (Carretta
et al. 2013). Most gray whales migrate past the mouth of Cook Inlet to
and from northern feeding grounds. However, small numbers of summering
gray whales have been noted by fisherman near Kachemak Bay and north of
Anchor Point. Further, summering gray whales were seen offshore of Cape
Starichkof by marine mammal observers monitoring Buccaneer's
Cosmopolitan drilling program in 2013 (Owl Ridge 2014). Regardless,
gray whales are not expected to be encountered in upper Cook Inlet,
where there are no records, but might be encountered during seismic
operations along the Kenai Peninsula south of Ninilchik. However,
seismic surveys are not planned in this region during the summer months
when gray whales are most expected.
Beluga Whale (Delphinapterus leucas)
The Cook Inlet beluga whale Distinct Population Segment (DPS) is a
small geographically isolated population that is separated from other
beluga populations by the Alaska Peninsula. The population is
genetically (mtDNA) distinct from other Alaska populations suggesting
the Peninsula is an effective barrier to genetic exchange (O'Corry-
Crowe et al. 1997) and that these whales may have been separated from
other stocks at least since the last ice age. Laidre et al. (2000)
examined data from more than 20 marine mammal surveys conducted in the
northern Gulf of Alaska and found that sightings of belugas outside
Cook Inlet were exceedingly rare, and these were composed of a few
stragglers from the Cook Inlet DPS observed at Kodiak Island, Prince
William Sound, and Yakutat Bay. Several marine mammal surveys specific
to Cook Inlet (Laidre et al. 2000, Speckman and Piatt 2000), including
those that concentrated on beluga whales (Rugh et al. 2000, 2005a),
clearly indicate that this stock largely confines itself to Cook Inlet.
There is no indication that these whales make forays into the Bering
Sea where they might intermix with other Alaskan stocks.
The Cook Inlet beluga DPS was originally estimated at 1,300 whales
in 1979 (Calkins 1989) and has been the focus of management concerns
since experiencing a dramatic decline in the 1990s. Between 1994 and
1998 the stock declined 47 percent which was attributed to
overharvesting by subsistence hunting. Subsistence hunting was
estimated to annually remove 10 to 15 percent of the population during
this period. Only five belugas have been harvested since 1999, yet the
population has continued to decline, with the most recent estimate at
only 312 animals (Allen and Angliss 2014). NMFS listed the population
as ``depleted'' in 2000 as a consequence of the decline, and as
``endangered'' under the Endangered Species Act (ESA) in 2008 when the
population failed to recover following a moratorium on subsistence
harvest. In April 2011, NMFS designated critical habitat for the beluga
under the ESA (Figure 3). The most recent aerial survey, conducted in
2014, suggests that the Cook Inlet population of belugas is comprised
of 340 individuals (Shelden et al, 2015).
Prior to the decline, this DPS was believed to range throughout
Cook Inlet and occasionally into Prince William Sound and Yakutat
(Nemeth et al. 2007). However the range has contracted coincident with
the population reduction (Speckman and Piatt 2000). During the summer
and fall beluga whales are concentrated near the Susitna River mouth,
Knik Arm, Turnagain Arm, and Chickaloon Bay (Nemeth et al. 2007) where
they feed on migrating eulachon (Thaleichthys paci[filig]cus) and
salmon (Onchorhyncus spp.) (Moore et al. 2000). Critical Habitat Area 1
reflects this summer distribution (Figure 5 in SAE Application). During
the winter, beluga whales concentrate in deeper waters in the mid-inlet
to Kalgin Island, and in the shallow waters along the west shore of
Cook Inlet to Kamishak Bay (Critical Habitat Area 2; Figure 5 in SAE
Application). Some whales may also winter in and near Kachemak Bay.
Harbor Porpoise (Phocoena phocoena)
Harbor porpoise are small (1.5 meters length), relatively
inconspicuous toothed whales. The Gulf of Alaska Stock is distributed
from Cape Suckling to Unimak Pass and was most recently estimated at
31,046 animals (Allen and Angliss 2014). They are found primarily in
coastal waters less than 100 meters (100 meters) deep (Hobbs and Waite
2010) where they feed on Pacific herring (Clupea pallasii), other
schooling fishes, and cephalopods.
Although they have been frequently observed during aerial surveys
in Cook Inlet, most sightings are of single animals, and are
concentrated at Chinitna and Tuxedni bays on the west side of lower
Cook Inlet (Rugh et al. 2005a). Dahlheim et al. (2000) estimated the
1991 Cook Inlet-wide population at only 136 animals. However, they are
one of the three marine mammals (besides belugas and harbor seals)
regularly seen in upper Cook Inlet (Nemeth et al. 2007), especially
during spring eulachon and summer salmon runs. Because harbor porpoise
have been observed throughout Cook Inlet during the summer months,
including mid-inlet waters, they could be encountered during seismic
operations in upper Cook Inlet.
Dall's Porpoise (Phocoenoides dalli)
Dall's porpoise are widely distributed throughout the North Pacific
Ocean including Alaska, although they are not found in upper Cook Inlet
and the shallower waters of the Bering, Chukchi, and Beaufort Seas
(Allen and Angliss 2014). Compared to harbor porpoise, Dall's porpoise
prefer the deep offshore and shelf slope waters. The Alaskan population
has been estimated at 83,400 animals (Allen and Angliss 2014), making
it one of the more common cetaceans in the state. Dall's porpoise have
been observed in lower Cook Inlet, including Kachemak Bay and near
Anchor Point (Owl Ridge 2014), but sightings there are rare. There is a
remote chance that Dall's porpoise might be encountered during seismic
operations along the Kenai Peninsula.
Killer Whale (Orcinus orca)
Two different stocks of killer whales inhabit the Cook Inlet region
of Alaska: The Alaska Resident Stock and the Gulf of Alaska, Aleutian
Islands, Bering Sea Transient Stock (Allen and Angliss 2014). The
resident stock is estimated at
[[Page 29171]]
2,347 animals and occurs from Southeast Alaska to the Bering Sea (Allen
and Angliss 2014). Resident whales feed exclusively on fish and are
genetically distinct from transient whales (Saulitis et al. 2000). The
transient whales feed primarily on marine mammals (Saulitis et al.
2000). The transient population inhabiting the Gulf of Alaska shares
mitochondrial DNA haplotypes with whales found along the Aleutian
Islands and the Bering Sea suggesting a common stock, although there
appears to be some subpopulation genetic structuring occurring to
suggest the gene flow between groups is limited (see Allen and Angliss
2014). For the three regions combined, the transient population has
been estimated at 587 animals (Allen and Angliss 2014).
Killer whales are occasionally observed in lower Cook Inlet,
especially near Homer and Port Graham (Shelden et al. 2003, Rugh et al.
2005a). A concentration of sightings near Homer and inside Kachemak Bay
may represent high use or may reflect high observer-effort, given most
records are from a whale-watching venture based in Homer. The few
whales that have been photographically identified in lower Cook Inlet
belong to resident groups more commonly found in nearby Kenai Fjords
and Prince William Sound (Shelden et al. 2003). Prior to the 1980s,
killer whale sightings in upper Cook Inlet were very rare. During
aerial surveys conducted between 1993 and 2004, killer whales were
observed on only three flights, all in the Kachemak and English Bay
area (Rugh et al. 2005a). However, anecdotal reports of killer whales
feeding on belugas in upper Cook Inlet began increasing in the 1990s,
possibly in response to declines in sea lion and harbor seal prey
elsewhere (Shelden et al. 2003). These sporadic ventures of transient
whales into beluga summering grounds have been implicated as a possible
contributor to decline of Cook Inlet belugas in the 1990s, although the
number of confirmed mortalities from killer whales is small (Shelden et
al. 2003). If killer whales were to venture into upper Cook Inlet in
2015, they might be encountered during both seismic operations in both
upper and lower Cook Inlet.
Steller Sea Lion (Eumetopia jubatus)
The Western Stock of the Steller sea lion is defined as all
populations west of longitude 144 [deg]W. to the western end of the
Aleutian Islands. The most recent estimate for this stock is 45,649
animals (Allen and Angliss 2014), considerably less than that estimated
140,000 animals in the 1950s (Merrick et al. 1987). Because of this
dramatic decline, the stock was listed under the ESA as a threatened
DPS in 1990, and relisted as endangered in 1997. Critical habitat was
designated in 1993, and is defined as a 20-nautical-mile radius around
all major rookeries and haulout sites. The 20-nautical-mile buffer was
established based on telemetry data that indicated these sea lions
concentrated their summer foraging effort within this distance of
rookeries and haul outs.
Steller sea lions inhabit lower Cook Inlet, especially in the
vicinity of Shaw Island and Elizabeth Island (Nagahut Rocks) haulout
sites (Rugh et al. 2005a), but are rarely seen in upper Cook Inlet
(Nemeth et al. 2007). Of the 42 Steller sea lion groups recorded during
Cook Inlet aerial surveys between 1993 and 2004, none were recorded
north of Anchor Point and only one in the vicinity of Kachemak Bay
(Rugh et al. 2005a). Marine mammal observers associated with
Buccaneer's drilling project off Cape Starichkof did observe seven
Steller sea lions during the summer of 2013 (Owl Ridge 2014).
The upper reaches of Cook Inlet may not provide adequate foraging
conditions for sea lions for establishing a major haul out presence.
Steller sea lions feed largely on walleye pollock (Theragra
chalcogramma), salmon (Onchorhyncus spp.), and arrowtooth flounder
(Atheresthes stomias) during the summer, and walleye pollock and
Pacific cod (Gadus macrocephalus) during the winter (Sinclair and
Zeppelin 2002), none of which, except for salmon, are found in
abundance in upper Cook Inlet (Nemeth et al. 2007). Steller sea lions
are unlikely to be encountered during seismic operations in upper Cook
Inlet, but they could possibly be encountered along the Kenai
Peninsula, especially closer to Anchor Point.
Harbor Seal (Phoca vitulina)
With more than 150,000 animals state-wide (Allen and Angliss 2014),
harbor seals are one of the more common marine mammal species in
Alaskan waters. They are most commonly seen hauled out at tidal flats
and rocky areas. Harbor seals feed largely on schooling fish such a
walleye pollock, Pacific cod, salmon, Pacific herring, eulachon, and
squid. Although harbor seals may make seasonal movements in response to
prey, they are resident to Alaska and do not migrate.
The Cook Inlet/Shelikof Stock, ranging from approximately Anchorage
down along the south side of the Alaska Peninsula to Unimak Pass, has
been recently estimated at a stable 22,900 (Allen and Angliss 2014).
Large numbers concentrate at the river mouths and embayments of lower
Cook Inlet, including the Fox River mouth in Kachemak Bay (Rugh et al.
2005a). Montgomery et al. (2007) recorded over 200 haulout sites in
lower Cook Inlet alone. However, only a few dozens to a couple hundred
seals seasonally occur in upper Cook Inlet (Rugh et al. 2005a), mostly
at the mouth of the Susitna River where their numbers vary in concert
with the spring eulachon and summer salmon runs (Nemeth et al. 2007,
Boveng et al. 2012). In 2012, up to 100 harbor seals were observed
hauled out at the mouths of the Theodore and Lewis rivers during
monitoring activity associated with SAE's (with Apache) 2012 Cook Inlet
seismic program. Montgomery et al. (2007) also found seals elsewhere in
Cook Inlet to move in response to local steelhead (Onchorhynchus
mykiss) and salmon runs. Harbor seals may be encountered during seismic
operations in both upper and lower Cook Inlet.
Potential Effects of the Specified Activity on Marine Mammals
This section includes a summary and discussion of the ways that
components (e.g., seismic airgun operations, vessel movement) of the
specified activity, including mitigation, may impact marine mammals.
The ``Estimated Take by Incidental Harassment'' section later in this
document will include a quantitative analysis of the number of
individuals that are expected to be taken by this activity. The
``Negligible Impact Analysis'' section will include the analysis of how
this specific activity will impact marine mammals and will consider the
content of this section, the ``Estimated Take by Incidental
Harassment'' section, the ``Mitigation'' section, and the ``Anticipated
Effects on Marine Mammal Habitat'' section to draw conclusions
regarding the likely impacts of this activity on the reproductive
success or survivorship of individuals and from that on the affected
marine mammal populations or stocks.
Operating active acoustic sources, such as airgun arrays, has the
potential for adverse effects on marine mammals. The majority of
anticipated impacts will be from the use of acoustic sources.
Acoustic Impacts
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 have been
[[Page 29172]]
derived using auditory evoked potentials, anatomical modeling, and
other data. Southall et al. (2007) designated ``functional hearing
groups'' for marine mammals and estimate the lower and upper
frequencies of functional hearing of the groups. The functional groups
and the associated frequencies are indicated below (note that animals
are less sensitive to sounds at the outer edge of their functional
range and most sensitive to sounds of frequencies within a smaller
range somewhere in the middle of their functional hearing range) and
have been modified slightly from Southall et al. 2007 to incorporate
some newer information:
Low frequency cetaceans (13 species of mysticetes):
functional hearing is estimated to occur between approximately 7 Hz and
30 kHz; (Ketten and Mountain 2009; Tubelli et al. 2012)
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; (Southall et al. 2007)
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; (Southall et al 2007)
Phocid pinnipeds in Water: Functional hearing is estimated
to occur between approximately 75 Hz and 100 kHz; (Hemil[auml] et al.
2006; Mulsow et al. 2011; Reichmuth et al. 2013) and
Otariid pinnipeds in Water: Functional hearing is
estimated to occur between approximately 100 Hz and 40 kHz. (Reichmuth
et al. 2013)
As mentioned previously in this document, nine marine mammal
species (seven cetacean and two pinniped species) are likely to occur
in the seismic survey area. Of the seven cetacean species likely to
occur in SAE's project area, three classified as a low-frequency
cetaceans (humpback, minke, gray whale), two are classified as mid-
frequency cetaceans (beluga and killer whales), and two are classified
as a high-frequency cetaceans (Dall's and harbor porpoise) (Southall et
al., 2007). Of the two pinniped species likely to occur in SAE's
project area, one is classified as a phocid (harbor seal), and one is
classified as an otariid (Steller sea lion). A species' functional
hearing group is a consideration when we analyze the effects of
exposure to sound on marine mammals.
1. Potential Effects of Airgun Sounds on Marine Mammals
The effects of sounds from airgun pulses might include one or more
of the following: Tolerance, masking of natural sounds, behavioral
disturbance, and temporary or permanent hearing impairment or non-
auditory effects (Richardson et al., 1995). As outlined in previous
NMFS documents, the effects of noise on marine mammals are highly
variable, often depending on species and contextual factors (based on
Richardson et al., 1995).
Tolerance: Numerous studies have shown that pulsed sounds from air
guns are often readily detectable in the water at distances of many
kilometers. Numerous studies have also shown that marine mammals at
distances more than a few kilometers from operating survey vessels
often show no apparent response. That is often true even in cases when
the pulsed sounds must be readily audible to the animals based on
measured received levels and the hearing sensitivity of that mammal
group. In general, pinnipeds and small odontocetes (toothed whales)
seem to be more tolerant of exposure to air gun pulses than baleen
whales. Although various toothed whales, and (less frequently)
pinnipeds have been shown to react behaviorally to airgun pulses under
some conditions, at other times, mammals of both types have shown no
overt reactions. Weir (2008) observed marine mammal responses to
seismic pulses from a 24 airgun array firing a total volume of either
5,085 in\3\ or 3,147 in\3\ in Angolan waters between August 2004 and
May 2005. Weir recorded a total of 207 sightings of humpback whales (n
= 66), sperm whales (n = 124), and Atlantic spotted dolphins (n = 17)
and reported that there were no significant differences in encounter
rates (sightings/hr) for humpback and sperm whales according to the
airgun array's operational status (i.e., active versus silent).
Behavioral Disturbance: Marine mammals may behaviorally respond
when exposed to anthropogenic noise. These behavioral reactions are
often shown as: Changing durations of surfacing and dives, number of
blows per surfacing, or moving direction and/or speed; reduced/
increased vocal activities; changing/cessation of certain behavioral
activities (such as socializing or feeding); visible startle response
or aggressive behavior (such as tail/fluke slapping or jaw clapping);
avoidance of areas where noise sources are located; and/or flight
responses (e.g., pinnipeds flushing into water from haulouts or
rookeries).
The biological significance of many of these behavioral
disturbances is difficult to predict. The consequences of behavioral
modification to individual fitness can range from none up to potential
changes to growth, survival, or reproduction, depending on the context,
duration, and degree of behavioral modification. Examples of behavioral
modifications that could impact growth, survival or reproduction
include: Drastic changes in diving/surfacing/swimming patterns that
lead to stranding (such as those associated with beaked whale
strandings related to exposure to military mid-frequency tactical
sonar); longer-term abandonment of habitat that is specifically
important for feeding, reproduction, or other critical needs, or
significant disruption of feeding or social interaction resulting in
substantive energetic costs, inhibited breeding, or prolonged or
permanent cow-calf separation.
The onset of behavioral disturbance from anthropogenic noise
depends on both external factors (characteristics of noise sources and
their paths) and the receiving animals (hearing, motivation,
experience, demography) and is also difficult to predict (Southall et
al., 2007).
Toothed whales. Few systematic data are available describing
reactions of toothed whales to noise pulses. However, systematic work
on sperm whales (Tyack et al., 2003) has yielded an increasing amount
of information about responses of various odontocetes to seismic
surveys based on monitoring studies (e.g., Stone, 2003; Smultea et al.,
2004; Moulton and Miller, 2005). Stone et al., 2003 reported reduced
sighting rates of small odontoceter during periods of shooting during
seismic surveys with large airgun arryas. Moulton and Miller (2004)
also found that the range of audibility of seismic pules for mid-sized
odontecetes was largely underestimated by models.
Seismic operators and marine mammal observers sometimes see
dolphins and other small toothed whales near operating airgun arrays,
but, in general, there seems to be a tendency for most delphinids to
show some limited avoidance of seismic vessels operating large airgun
systems. However, some dolphins seem to be attracted to the seismic
vessel and floats, and some ride the bow wave of the seismic vessel
even when large arrays of airguns are firing. Nonetheless, there have
been indications that small toothed whales sometimes move away or
maintain a somewhat greater distance from the vessel when a large array
of airguns is operating than when it is
[[Page 29173]]
silent (e.g., Goold, 1996a,b,c; Calambokidis and Osmek, 1998; Stone,
2003). The beluga may be a species that (at least in certain geographic
areas) shows long-distance avoidance of seismic vessels. Aerial surveys
during seismic operations in the southeastern Beaufort Sea recorded
much lower sighting rates of beluga whales within 10-20 km (6.2-12.4
mi) of an active seismic vessel. These results were consistent with the
low number of beluga sightings reported by observers aboard the seismic
vessel, suggesting that some belugas might have been avoiding the
seismic operations at distances of 10-20 km (6.2-12.4 mi) (Miller et
al., 2005).
Captive bottlenose dolphins and (of more relevance in this project)
beluga whales exhibit changes in behavior when exposed to strong pulsed
sounds similar in duration to those typically used in seismic surveys
(Finneran et al., 2002, 2005). However, the animals tolerated high
received levels of sound (pk-pk level >200 dB re 1 [mu]Pa) before
exhibiting aversive behaviors.
Observers stationed on seismic vessels operating off the United
Kingdom from 1997-2000 have provided data on the occurrence and
behavior of various toothed whales exposed to seismic pulses (Stone,
2003; Gordon et al., 2004). Killer whales were found to be
significantly farther from large airgun arrays during periods of
shooting compared with periods of no shooting. The displacement of the
median distance from the array was approximately 0.5 km (0.3 mi) or
more. Killer whales also appear to be more tolerant of seismic shooting
in deeper water.
Reactions of toothed whales to large arrays of airguns are variable
and, at least for delphinids, seem to be confined to a smaller radius
than has been observed for mysticetes. However, based on the limited
existing evidence, belugas should not necessarily generally be grouped
with delphinids in the ``less responsive'' category.
Pinnipeds. Pinnipeds are not likely to show a strong avoidance
reaction to the airgun sources used. Visual monitoring from seismic
vessels has shown only slight (if any) avoidance of airguns by
pinnipeds and only slight (if any) changes in behavior. Monitoring work
in the Alaskan Beaufort Sea during 1996-2001 provided considerable
information regarding the behavior of Arctic ice seals exposed to
seismic pulses (Harris et al., 2001; Moulton and Lawson, 2002). These
seismic projects usually involved arrays of 6 to 16 airguns with total
volumes of 560 to 1,500 in\3\. The combined results suggest that some
seals avoid the immediate area around seismic vessels. In most survey
years, ringed seal sightings tended to be farther away from the seismic
vessel when the airguns were operating than when they were not (Moulton
and Lawson, 2002). However, these avoidance movements were relatively
small, on the order of 100 m (328 ft) to a few hundreds of meters, and
many seals remained within 100-200 m (328-656 ft) of the trackline as
the operating airgun array passed by. Seal sighting rates at the water
surface were lower during airgun array operations than during no-airgun
periods in each survey year except 1997. Similarly, seals are often
very tolerant of pulsed sounds from seal-scaring devices (Mate and
Harvey, 1987; Jefferson and Curry, 1994; Richardson et al., 1995a).
However, initial telemetry work suggests that avoidance and other
behavioral reactions by two other species of seals, grey and harbor
seals, to small airgun sources may at times be stronger than evident to
date from visual studies of pinniped reactions to airguns (Thompson et
al., 1998). Even if reactions of the species occurring in the activity
area are as strong as those evident in the telemetry study, reactions
are expected to be confined to relatively small distances and
durations, with no long-term effects on pinniped individuals or
populations.
Masking: Masking is the obscuring of sounds of interest by other
sounds, often at similar frequencies. Marine mammals use acoustic
signals for a variety of purposes, which differ among species, but
include communication between individuals, navigation, foraging,
reproduction, avoiding predators, and learning about their environment
(Erbe and Farmer, 2000; Tyack, 2000). Masking, or auditory
interference, generally occurs when sounds in the environment are
louder than, and of a similar frequency to, auditory signals an animal
is trying to receive. Masking is a phenomenon that affects animals
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.
Masking occurs when anthropogenic sounds and signals (that the
animal utilizes) overlap at both spectral and temporal scales. For the
airgun sound generated from the seismic surveys, sound will consist of
low frequency (under 500 Hz) pulses with extremely short durations
(less than one second). Lower frequency man-made sounds are more likely
to affect detection of potentially important natural sounds such as
surf and prey noise, or communication calls for low frequency
specialists. There is little concern regarding masking near the sound
source due to the brief duration of these pulses and relatively longer
silence between air gun shots (approximately 12 seconds). However, at
long distances (over tens of kilometers away), due to multipath
propagation and reverberation, the durations of airgun pulses can be
``stretched'' to seconds with long decays (Madsen et al., 2006),
although the intensity of the sound is greatly reduced.
This could affect communication signals used by low frequency
mysticetes when they occur near the noise band and thus reduce the
communication space of animals (e.g., Clark et al., 2009) and cause
increased stress levels (e.g., Foote et al., 2004; Holt et al., 2009);
however, no baleen whales are expected to occur within the action area.
Marine mammals are thought to be able to compensate for masking by
adjusting their acoustic behavior by shifting call frequencies, and/or
increasing call volume and vocalization rates. For example, blue whales
were found to increase call rates when exposed to seismic survey noise
in the St. Lawrence Estuary (Di Iorio and Clark, 2010). The North
Atlantic right whales (Eubalaena glacialis) exposed to high shipping
noise increase call frequency (Parks et al., 2007), while some humpback
whales respond to low-frequency active sonar playbacks by increasing
song length (Miller et al., 2000). Additionally, beluga whales have
been known to change their vocalizations in the presence of high
background noise possibly to avoid masking calls (Au et al., 1985;
Lesage et al., 1999; Scheifele et al., 2005). Although some degree of
masking is inevitable when high levels of manmade broadband sounds are
introduced into the sea, marine mammals have evolved systems and
behavior that function to reduce the impacts of masking. Structured
signals, such as the echolocation click sequences of small toothed
whales, may be readily detected even in the presence of strong
background noise because their frequency content and temporal features
usually differ strongly from those of the background noise (Au and
Moore, 1988, 1990). The components of background noise that are similar
in frequency to the sound signal in question primarily determine the
degree of masking of that signal.
[[Page 29174]]
Redundancy and context can also facilitate detection of weak
signals. These phenomena may help marine mammals detect weak sounds in
the presence of natural or manmade noise. Most masking studies in
marine mammals present the test signal and the masking noise from the
same direction. The sound localization abilities of marine mammals
suggest that, if signal and noise come from different directions,
masking would not be as severe as the usual types of masking studies
might suggest (Richardson et al., 1995). The dominant background noise
may be highly directional if it comes from a particular anthropogenic
source such as a ship or industrial site. Directional hearing may
significantly reduce the masking effects of these sounds by improving
the effective signal-to-noise ratio. In the cases of higher frequency
hearing by the bottlenose dolphin, beluga whale, and killer whale,
empirical evidence confirms that masking depends strongly on the
relative directions of arrival of sound signals and the masking noise
(Penner et al., 1986; Dubrovskiy, 1990; Bain et al., 1993; Bain and
Dahlheim, 1994). Toothed whales and probably other marine mammals as
well, have additional capabilities besides directional hearing that can
facilitate detection of sounds in the presence of background noise.
There is evidence that some toothed whales can shift the dominant
frequencies of their echolocation signals from a frequency range with a
lot of ambient noise toward frequencies with less noise (Au et al.,
1974, 1985; Moore and Pawloski, 1990; Thomas and Turl, 1990; Romanenko
and Kitain, 1992; Lesage et al., 1999). A few marine mammal species are
known to increase the source levels or alter the frequency of their
calls in the presence of elevated sound levels (Dahlheim, 1987; Au,
1993; Lesage et al., 1993, 1999; Terhune, 1999; Foote et al., 2004;
Parks et al., 2007, 2009; Di Iorio and Clark, 2009; Holt et al., 2009).
These data demonstrating adaptations for reduced masking pertain
mainly to the very high frequency echolocation signals of toothed
whales. There is less information about the existence of corresponding
mechanisms at moderate or low frequencies or in other types of marine
mammals. For example, Zaitseva et al. (1980) found that, for the
bottlenose dolphin, the angular separation between a sound source and a
masking noise source had little effect on the degree of masking when
the sound frequency was 18 kHz, in contrast to the pronounced effect at
higher frequencies. Directional hearing has been demonstrated at
frequencies as low as 0.5-2 kHz in several marine mammals, including
killer whales (Richardson et al., 1995a). This ability may be useful in
reducing masking at these frequencies. In summary, high levels of sound
generated by anthropogenic activities may act to mask the detection of
weaker biologically important sounds by some marine mammals. This
masking may be more prominent for lower frequencies. For higher
frequencies, such as that used in echolocation by toothed whales,
several mechanisms are available that may allow them to reduce the
effects of such masking.
Threshold Shift (noise-induced loss of hearing)--When animals
exhibit reduced hearing sensitivity (i.e., sounds must be louder for an
animal to detect them) following exposure to an intense sound or sound
for long duration, it is referred to as a noise-induced threshold shift
(TS). An animal can experience temporary threshold shift (TTS) or
permanent threshold shift (PTS). TTS can last from minutes or hours to
days (i.e., there is complete recovery), can occur in specific
frequency ranges (i.e., an animal might only have a temporary loss of
hearing sensitivity between the frequencies of 1 and 10 kHz), and can
be of varying amounts (for example, an animal's hearing sensitivity
might be reduced initially by only 6 dB or reduced by 30 dB). PTS is
permanent, but some recovery is possible. PTS can also occur in a
specific frequency range and amount as mentioned above for TTS.
The following physiological mechanisms are thought to play a role
in inducing auditory TS: Effects to sensory hair cells in the inner ear
that reduce their sensitivity, modification of the chemical environment
within the sensory cells, residual muscular activity in the middle ear,
displacement of certain inner ear membranes, increased blood flow, and
post-stimulatory reduction in both efferent and sensory neural output
(Southall et al., 2007). The amplitude, duration, frequency, temporal
pattern, and energy distribution of sound exposure all can affect the
amount of associated TS and the frequency range in which it occurs. As
amplitude and duration of sound exposure increase, so, generally, does
the amount of TS, along with the recovery time. For intermittent
sounds, less TS could occur than compared to a continuous exposure with
the same energy (some recovery could occur between intermittent
exposures depending on the duty cycle between sounds) (Kryter et al.,
1966; Ward, 1997). For example, one short but loud (higher SPL) sound
exposure may induce the same impairment as one longer but softer sound,
which in turn may cause more impairment than a series of several
intermittent softer sounds with the same total energy (Ward, 1997).
Additionally, though TTS is temporary, prolonged exposure to sounds
strong enough to elicit TTS, or shorter-term exposure to sound levels
well above the TTS threshold, can cause PTS, at least in terrestrial
mammals (Kryter, 1985). In the case of the seismic survey, 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 papers on hearing
impairments that can occur with exposure to a loud sound, only a few
studies provide empirical information on the levels at which noise-
induced loss in hearing sensitivity occurs in nonhuman animals. For
marine mammals, published data are limited to the captive bottlenose
dolphin, beluga, harbor porpoise, and Yangtze finless porpoise
(Finneran et al., 2000, 2002, 2003, 2005, 2007, 2010a, 2010b; Finneran
and Schlundt, 2010; Lucke et al., 2009; Mooney et al., 2009a, 2009b;
Popov et al., 2011a, 2011b; Kastelein et al., 2012a; Schlundt et al.,
2000; Nachtigall et al., 2003, 2004). For pinnipeds in water, data are
limited to measurements of TTS in harbor seals, an elephant seal, and
California sea lions (Kastak et al., 1999, 2005; Kastelein et al.,
2012b).
Marine mammal hearing plays a critical role in communication with
conspecifics, and interpretation of environmental cues for purposes
such as predator avoidance and prey capture. Depending on the degree
(elevation of threshold in dB), duration (i.e., recovery time), and
frequency range of TTS, and the context in which it is experienced, TTS
can have effects on marine mammals ranging from discountable to serious
(similar to those discussed in auditory masking, below). For example, a
marine mammal may be able to readily compensate for a brief, relatively
small amount of TTS in a non-critical frequency range that occurs
during a time where ambient noise is lower and
[[Page 29175]]
there are not as many competing sounds present. Alternatively, a larger
amount and longer duration of TTS sustained during time when
communication is critical for successful mother/calf interactions could
have more serious impacts. Similarly, depending on the degree and
frequency range, the effects of PTS on an animal could range in
severity, although it is considered generally more serious because it
is a permanent condition. Of note, reduced hearing sensitivity as a
simple function of aging has been observed in marine mammals, as well
as humans and other taxa (Southall et al., 2007), so we can infer that
strategies exist for coping with this condition to some degree, though
likely not without cost.
Given the higher level of sound necessary to cause PTS as compared
with TTS, it is considerably less likely that PTS would occur during
the seismic surveys in Cook Inlet. Cetaceans generally avoid the
immediate area around operating seismic vessels, as do some other
marine mammals. Some pinnipeds show avoidance reactions to airguns, but
their avoidance reactions are generally not as strong or consistent as
those of cetaceans, and occasionally they seem to be attracted to
operating seismic vessels (NMFS, 2010).
Non-auditory Physical Effects: Non-auditory physical effects might
occur in marine mammals exposed to strong underwater pulsed sound.
Possible types of non-auditory physiological effects or injuries that
theoretically might occur in mammals close to a strong sound source
include stress, neurological effects, bubble formation, and other types
of organ or tissue damage. Some marine mammal species (i.e., beaked
whales) may be especially susceptible to injury and/or stranding when
exposed to strong pulsed sounds.
Classic stress responses begin when an animal's central nervous
system perceives a potential threat to its homeostasis. That perception
triggers stress responses regardless of whether a stimulus actually
threatens the animal; the mere perception of a threat is sufficient to
trigger a stress response (Moberg, 2000; Sapolsky et al., 2005; Seyle,
1950). Once an animal's central nervous system perceives a threat, it
mounts a biological response or defense that consists of a combination
of the four general biological defense responses: Behavioral responses;
autonomic nervous system responses; neuroendocrine responses; or immune
responses.
In the case of many stressors, an animal's first and most
economical (in terms of biotic costs) response is behavioral avoidance
of the potential stressor or avoidance of continued exposure to a
stressor. An animal's second line of defense to stressors involves the
sympathetic part of the autonomic nervous system and the classical
``fight or flight'' response, which includes the cardiovascular system,
the gastrointestinal system, the exocrine glands, and the adrenal
medulla to produce changes in heart rate, blood pressure, and
gastrointestinal activity that humans commonly 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
neuroendocrine functions that are affected by stress--including immune
competence, reproduction, metabolism, and behavior--are regulated by
pituitary hormones. Stress-induced changes in the secretion of
pituitary hormones have been implicated in failed reproduction (Moberg,
1987; Rivier, 1995), altered metabolism (Elasser et al., 2000), reduced
immune competence (Blecha, 2000), and behavioral disturbance. Increases
in the circulation of glucocorticosteroids (cortisol, corticosterone,
and aldosterone in marine mammals; see Romano et al., 2004) have been
equated with stress for many years.
The primary distinction between stress (which is adaptive and does
not normally place an animal at risk) and distress is the biotic cost
of the response. During a stress response, an animal uses glycogen
stores that can be quickly replenished once the stress is alleviated.
In such circumstances, the cost of the stress response would not pose a
risk to the animal's welfare. However, when an animal does not have
sufficient energy reserves to satisfy the energetic costs of a stress
response, energy resources must be diverted from other biotic
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 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. Note that these examples involved a long-
term (days or weeks) stress response due to exposure to stimuli.
Relationships between these physiological mechanisms, animal
behavior, and the costs of stress responses have also been documented
fairly well through controlled experiment; 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 anthropogenic sound exposure, 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 anthropogenic sounds.
For example, Jansen (1998) reported on the relationship between
acoustic exposures and physiological responses that are indicative of
stress responses in humans (e.g., 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 (i.e., goldfish) that accompanied short- and
long-term hearing losses. Welch and Welch (1970) reported physiological
and behavioral stress responses that accompanied damage to the inner
ears of fish and several mammals.
Hearing is one of the primary senses marine mammals use to gather
information about their environment and communicate with conspecifics.
Although empirical information on the effects of sensory impairment
(TTS, PTS, and acoustic masking) on marine mammals remains limited, we
assume
[[Page 29176]]
that reducing a marine mammal's ability to gather information about its
environment and communicate with other members of its species would
induce stress, based on data that terrestrial animals exhibit those
responses under similar conditions (NRC, 2003) and because marine
mammals 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. However, marine
mammals also 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),
NMFS also assumes that stress responses could 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. Resonance effects (Gentry, 2002) and
direct noise-induced bubble formations (Crum et al., 2005) are
implausible in the case of exposure to an impulsive broadband source
like an airgun array. If seismic surveys disrupt diving patterns of
deep-diving species, this might result in bubble formation and a form
of the bends, as speculated to occur in beaked whales exposed to sonar.
However, there is no specific evidence of this upon exposure to airgun
pulses. Additionally, no beaked whale species occur in the seismic
survey area.
In general, very little is known about the potential for strong,
anthropogenic underwater sounds to cause non-auditory physical effects
in marine mammals. Such effects, if they occur at all, would presumably
be limited to short distances and to activities that extend over a
prolonged period. The available data do not allow identification of a
specific exposure level above which non-auditory effects can be
expected (Southall et al., 2007) or any meaningful quantitative
predictions of the numbers (if any) of marine mammals that might be
affected in those ways. There is no definitive evidence that any of
these effects occur even for marine mammals in close proximity to large
arrays of airguns. In addition, marine mammals that show behavioral
avoidance of seismic vessels, including belugas and some pinnipeds, are
especially unlikely to incur non-auditory impairment or other physical
effects. Therefore, it is unlikely that such effects would occur during
SAE's surveys given the brief duration of exposure and the planned
monitoring and mitigation measures described later in this document.
Stranding and Mortality: Marine mammals close to underwater
detonations of high explosive can be killed or severely injured, and
the auditory organs are especially susceptible to injury (Ketten et al.
1993; Ketten 1995). Airgun pulses are less energetic and their peak
amplitudes have slower rise times. To date, there is no evidence that
serious injury, death, or stranding by marine mammals can occur from
exposure to air gun pulses, even in the case of large air gun arrays.
However, in past IHA notices for seismic surveys, commenters have
referenced two stranding events allegedly associated with seismic
activities, one off Baja California and a second off Brazil. NMFS has
addressed this concern several times, including in the Federal Register
notice announcing the IHA for Apache Alaska's first seismic survey in
2012. Readers are encouraged to review NMFS's response to comments on
this matter found in 69 FR 74905 (December 14, 2004), 71 FR 43112 (July
31, 2006), 71 FR 50027 (August 24, 2006), 71 FR 49418 (August 23,
2006), and 77 FR 27720 (May 11, 2012).
Beluga whale strandings in Cook Inlet are not uncommon; however,
these events often coincide with extreme tidal fluctuations (``spring
tides'') or killer whale sightings (Shelden et al., 2003). For example,
in August 2012, a group of Cook Inlet beluga whales stranded in the mud
flats of Turnagain Arm during low tide and were able to swim free with
the flood tide. No strandings or marine mammals in distress were
observed during the 2D test survey conducted by Apache in March 2011,
and none were reported by Cook Inlet inhabitants. As a result, NMFS
does not expect any marine mammals will incur serious injury or
mortality in Cook Inlet or strand as a result of the seismic survey.
2. Potential Effects From Pingers on Marine Mammals
Active acoustic sources other than the airguns will be used for
SAE's oil and gas exploration seismic survey program in Cook Inlet. The
specifications for the pingers (source levels and frequency ranges)
were provided earlier in this document. In general, pingers are known
to cause behavioral disturbance and are commonly used to deter marine
mammals from commercial fishing gear or fish farms. Due to the
potential to change marine mammal behavior, shut downs described for
airguns will also be applied to pinger use.
Vessel Impacts
Vessel activity and noise associated with vessel activity will
temporarily increase in the action area during SAE's seismic survey as
a result of the operation of nine vessels. To minimize the effects of
vessels and noise associated with vessel activity, SAE will follow
NMFS's Marine Mammal Viewing Guidelines and Regulations and will alter
heading or speed if a marine mammal gets too close to a vessel. In
addition, vessels will be operating at slow speed (4-5 knots) when
conducting surveys and in a purposeful manner to and from work sites in
as direct a route as possible. Marine mammal monitoring observers and
passive acoustic devices will alert vessel captains as animals are
detected to ensure safe and effective measures are applied to avoid
coming into direct contact with marine mammals. Therefore, NMFS neither
anticipates nor authorizes takes of marine mammals from ship strikes.
Odontocetes, such as beluga whales, killer whales, and harbor
porpoises, often show tolerance to vessel activity; however, they may
react at long distances if they are confined by ice, shallow water, or
were previously harassed by vessels (Richardson et al., 1995). Beluga
whale response to vessel noise varies greatly from tolerance to extreme
sensitivity depending on the activity of the whale and previous
experience with vessels (Richardson et al., 1995). Reactions to vessels
depend on whale activities and experience, habitat, boat type, and boat
behavior (Richardson et al., 1995) and may include behavioral
responses, such as altered headings or avoidance (Blane and Jaakson,
1994; Erbe and Farmer, 2000); fast swimming; changes in vocalizations
(Lesage et al., 1999; Scheifele et al., 2005); and changes in dive,
surfacing, and respiration patterns.
There are few data published on pinniped responses to vessel
activity, and most of the information is anecdotal (Richardson et al.,
1995). Generally, sea lions in water show tolerance to close and
frequently approaching vessels and sometimes show interest in fishing
vessels. They are less tolerant when hauled out on land; however, they
rarely react unless the vessel approaches within 100-200 m (330-660 ft;
reviewed in Richardson et al., 1995).
Entanglement
Although some of SAE's equipment contains cables or lines, the risk
of entanglement is extremely remote. Additionally, mortality from
entanglement is not anticipated. The
[[Page 29177]]
material used by SAE and the amount of slack is not anticipated to
allow for marine mammal entanglements.
Anticipated Effects on Marine Mammal Habitat
The primary potential impacts to marine mammal habitat and other
marine species are associated with elevated sound levels produced by
airguns and other active acoustic sources. However, other potential
impacts to the surrounding habitat from physical disturbance are also
possible. This section describes the potential impacts to marine mammal
habitat from the specified activity. Because the marine mammals in the
area feed on fish and/or invertebrates there is also information on the
species typically preyed upon by the marine mammals in the area. As
noted earlier, upper Cook Inlet is an important feeding and calving
area for the Cook Inlet beluga whale and critical habitat has been
designated for this species in the seismic survey area.
Common Marine Mammal Prey in the Project Area
Fish are the primary prey species for marine mammals in upper Cook
Inlet. Beluga whales feed on a variety of fish, shrimp, squid, and
octopus (Burns and Seaman, 1986). Common prey species in Knik Arm
include salmon, eulachon and cod. Harbor seals feed on fish such as
pollock, cod, capelin, eulachon, Pacific herring, and salmon, as well
as a variety of benthic species, including crabs, shrimp, and
cephalopods. Harbor seals are also opportunistic feeders with their
diet varying with season and location. The preferred diet of the harbor
seal in the Gulf of Alaska consists of pollock, octopus, capelin,
eulachon, and Pacific herring (Calkins, 1989). Other prey species
include cod, flat fishes, shrimp, salmon, and squid (Hoover, 1988).
Harbor porpoises feed primarily on Pacific herring, cod, whiting
(hake), pollock, squid, and octopus (Leatherwood et al., 1982). In the
upper Cook Inlet area, harbor porpoise feed on squid and a variety of
small schooling fish, which would likely include Pacific herring and
eulachon (Bowen and Siniff, 1999; NMFS, unpublished data). Killer
whales feed on either fish or other marine mammals depending on genetic
type (resident versus transient respectively). Killer whales in Knik
Arm are typically the transient type (Shelden et al., 2003) and feed on
beluga whales and other marine mammals, such as harbor seal and harbor
porpoise. The Steller sea lion diet consists of a variety of fishes
(capelin, cod, herring, mackerel, pollock, rockfish, salmon, sand
lance, etc.), bivalves, squid, octopus, and gastropods.
Potential Impacts on Prey Species
With regard to fish as a prey source for cetaceans and pinnipeds,
fish are known to hear and react to sounds and to use sound to
communicate (Tavolga et al., 1981) and possibly avoid predators (Wilson
and Dill, 2002). Experiments have shown that fish can sense both the
strength and direction of sound (Hawkins, 1981). Primary factors
determining whether a fish can sense a sound signal, and potentially
react to it, are the frequency of the signal and the strength of the
signal in relation to the natural background sound level.
Fishes produce sounds that are associated with behaviors that
include territoriality, mate search, courtship, and aggression. It has
also been speculated that sound production may provide the means for
long distance communication and communication under poor underwater
visibility conditions (Zelick et al., 1999), although the fact that
fish communicate at low-frequency sound levels where the masking
effects of ambient noise are naturally highest suggests that very long
distance communication would rarely be possible. Fishes have evolved a
diversity of sound generating organs and acoustic signals of various
temporal and spectral contents. Fish sounds vary in structure,
depending on the mechanism used to produce them (Hawkins, 1993).
Generally, fish sounds are predominantly composed of low frequencies
(less than 3 kHz).
Since objects in the water scatter sound, fish are able to detect
these objects through monitoring the ambient noise. Therefore, fish are
probably able to detect prey, predators, conspecifics, and physical
features by listening to environmental sounds (Hawkins, 1981). There
are two sensory systems that enable fish to monitor the vibration-based
information of their surroundings. The two sensory systems, the inner
ear and the lateral line, constitute the acoustico-lateralis system.
Although the hearing sensitivities of very few fish species have
been studied to date, it is becoming obvious that the intra- and inter-
specific variability is considerable (Coombs, 1981). Nedwell et al.
(2004) compiled and published available fish audiogram information. A
noninvasive electrophysiological recording method known as auditory
brainstem response is now commonly used in the production of fish
audiograms (Yan, 2004). Popper and Carlson (1998) and the Navy (2001)
found that fish generally perceive underwater sounds in the frequency
range of 50-2,000 Hz, with peak sensitivities below 800 Hz. Even though
some fish are able to detect sounds in the ultrasonic frequency range,
the thresholds at these higher frequencies tend to be considerably
higher than those at the lower end of the auditory frequency range.
Fish are sensitive to underwater impulsive sounds due to swim
bladder resonance. As the pressure wave passes through a fish, the swim
bladder is rapidly squeezed as the high pressure wave, and then the
under pressure component of the wave, passes through the fish. The swim
bladder may repeatedly expand and contract at the high sound pressure
levels, creating pressure on the internal organs surrounding the swim
bladder.
Literature relating to the impacts of sound on marine fish species
can be divided into the following categories: (1) Pathological effects;
(2) physiological effects; and (3) behavioral effects. Pathological
effects include lethal and sub-lethal physical damage to fish;
physiological effects include primary and secondary stress responses;
and behavioral effects include changes in exhibited behaviors of fish.
Behavioral changes might be a direct reaction to a detected sound or a
result of the anthropogenic sound masking natural sounds that the fish
normally detect and to which they respond. The three types of effects
are often interrelated in complex ways. For example, some physiological
and behavioral effects could potentially lead to the ultimate
pathological effect of mortality. Hastings and Popper (2005) reviewed
what is known about the effects of sound on fishes and identified
studies needed to address areas of uncertainty relative to measurement
of sound and the responses of fishes. Popper et al. (2003/2004) also
published a paper that reviews the effects of anthropogenic sound on
the behavior and physiology of fishes.
The level of sound at which a fish will react or alter its behavior
is usually well above the detection level. Fish have been found to
react to sounds when the sound level increased to about 20 dB above the
detection level of 120 dB (Ona, 1988); however, the response threshold
can depend on the time of year and the fish's physiological condition
(Engas et al., 1993). In general, fish react more strongly to pulses of
sound rather than a continuous signal (Blaxter et al., 1981), and a
quicker alarm response is elicited when the sound signal intensity
rises rapidly compared to sound rising more slowly to the same level.
[[Page 29178]]
Investigations of fish behavior in relation to vessel noise (Olsen
et al., 1983; Ona, 1988; Ona and Godo, 1990) have shown that fish react
when the sound from the engines and propeller exceeds a certain level.
Avoidance reactions have been observed in fish such as cod and herring
when vessels approached close enough that received sound levels are 110
dB to 130 dB (Nakken, 1992; Olsen, 1979; Ona and Godo, 1990; Ona and
Toresen, 1988). However, other researchers have found that fish such as
polar cod, herring, and capelin are often attracted to vessels
(apparently by the noise) and swim toward the vessel (Rostad et al.,
2006). Typical sound source levels of vessel noise in the audible range
for fish are 150 dB to 170 dB (Richardson et al., 1995).
Carlson (1994), in a review of 40 years of studies concerning the
use of underwater sound to deter salmonids from hazardous areas at
hydroelectric dams and other facilities, concluded that salmonids were
able to respond to low-frequency sound and to react to sound sources
within a few feet of the source. He speculated that the reason that
underwater sound had no effect on salmonids at distances greater than a
few feet is because they react to water particle motion/acceleration,
not sound pressures. Detectable particle motion is produced within very
short distances of a sound source, although sound pressure waves travel
farther.
Potential Impacts to the Benthic Environment
SAE's seismic survey requires the deployment of a submersible
recording system in the inter-tidal and marine zones. An autonomous
``nodal'' (i.e., no cables) system would be placed on the seafloor by
specific vessels in lines parallel to each other with a node line
spacing of 402 m (0.25 mi). Each nodal ``patch'' will have 32 node
lines parallel to each other. The lines generally run perpendicular to
the shoreline. An entire patch will be placed on the seafloor prior to
airgun activity. As the patches are surveyed, the node lines will be
moved either side to side or inline to the next location. Placement and
retrieval of the nodes may cause temporary and localized increases in
turbidity on the seafloor. The substrate of Cook Inlet consists of
glacial silt, clay, cobbles, pebbles, and sand (Sharma and Burrell,
1970). Sediments like sand and cobble dissipate quickly when suspended,
but finer materials like clay and silt can create thicker plumes that
may harm fish; however, the turbidity created by placing and removing
nodes on the seafloor will settle to background levels within minutes
after the cessation of activity.
In addition, seismic noise will radiate throughout the water column
from airguns and pingers until it dissipates to background levels. No
studies have demonstrated that seismic noise affects the life stages,
condition, or amount of food resources (fish, invertebrates, eggs) used
by marine mammals, except when exposed to sound levels within a few
meters of the seismic source or in few very isolated cases. NMFS has
also required a seasonal closure near the Susitna River Delta from
April 15 to October 15, which is an essential foraging location for
Cook Inlet belugas. Where fish or invertebrates did respond to seismic
noise, the effects were temporary and of short duration. Consequently,
disturbance to fish species due to the activities associated with the
seismic survey (i.e, placement and retrieval of nodes and noise from
sound sources) will be short term and fish will be expected to return
to their pre-disturbance behavior once seismic survey activities cease.
Based on the preceding discussion, the activity is not expected to
have any habitat-related effects that could cause significant or long-
term consequences for individual marine mammals or their populations.
Mitigation
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 impact on such species or stock and its
habitat, paying particular attention to rookeries, mating grounds, and
areas of similar significance, and on the availability of such species
or stock for taking for certain subsistence uses (where relevant).
Mitigation Measures in SAE's Application
For the mitigation measures, SAE listed the following protocols to
be implemented during its seismic survey program in Cook Inlet.
1. Operation of Mitigation Airgun at Night
SAE will conduct both daytime and nighttime operations. Nighttime
operations will be initiated only if a ``mitigation airgun'' (typically
the 10 in\3\) has been continuously operational from the time that PSO
monitoring has ceased for the day. Seismic activity will not ramp up
from an extended shut-down (i.e., when the airgun has been down with no
activity for at least 10 minutes) during nighttime operations, and
survey activities will be suspended until the following day. At night,
the vessel captain and crew will maintain lookout for marine mammals
and will order the airgun(s) to be shut down if marine mammals are
observed in or about to enter the established exclusion zones.
2. Exclusion and Disturbance Zones
SAE will establish exclusion zones to avoid Level A harassment
(``injury exclusion zone'') of all marine mammals and to avoid Level B
harassment (``disturbance exclusion zone'') of any beluga whales or
groups of five or more killer whales or harbor porpoises detected
within the designated zones. The injury exclusion zone will correspond
to the area around the source within which received levels equal or
exceed 180 dB re 1 [micro]Pa [rms] for cetaceans and 190 dB re 1
[micro]Pa [rms] for pinnipeds, and SAE will shut down or power down
operations if any marine mammals are seen approaching or entering this
zone (more detail below). The disturbance exclusion zone will
correspond to the area around the source within which received levels
equal or exceed 160 dB re 1 [micro]Pa [rms] and SAE will implement
power down and/or shutdown measures, as appropriate, if any beluga
whales, humpback whales, Steller sea lions, or group of five or more
killer whales or harbor porpoises are seen entering or approaching the
disturbance exclusion zone.
3. Power Down and Shutdown Procedures
A power down is the immediate reduction in the number of operating
energy sources from a full array firing to a mitigation airgun. A
shutdown is the immediate cessation of firing of all energy sources.
The arrays will be immediately powered down whenever a marine mammal is
sighted approaching close to or within the applicable exclusion zone of
the full arrays but is outside the applicable exclusion zone of the
single source. If a marine mammal is sighted within the applicable
exclusion zone of the single energy source, the entire array will be
shutdown (i.e., no sources firing). Following a power down or a
shutdown, airgun activity will not resume until the marine mammal has
clearly left the applicable injury or disturbance exclusion zone. The
animal will be considered to have cleared the zone if it: (1) Is
visually observed to have left the zone; (2) has not been seen within
the zone for 15 minutes in the case of pinnipeds and small odontocetes;
or (3)
[[Page 29179]]
has not been seen within the zone for 30 minutes in the case of large
odontocetes, including killer whales and belugas.
Visual monitoring by qualified PSOs will continue for 30 minutes
after a shutdown or at the end of a period of seismic surveying to
monitor for animals returning to the previously ensonified area.
4. Ramp-Up Procedures
A ramp-up of an airgun array provides a gradual increase in sound
levels, and involves a step-wise increase in the number and total
volume of air guns firing until the full volume is achieved. The
purpose of a ramp-up (or ``soft start'') is to ``warn'' cetaceans and
pinnipeds in the vicinity of the airguns and to provide the time for
them to leave the area and thus avoid any potential injury or
impairment of their hearing abilities.
During the seismic survey, the seismic operator will ramp up the
airgun array slowly at a rate of no more than 6 dB per 5-minute period.
Ramp-up is used at the start of airgun operations, after a power- or
shut-down, and after any period of greater than 10 minutes in duration
without airgun operations (``extended shutdown'').
A full ramp-up after a shutdown will not begin until there has been
a minimum of 30 minutes of observation of the applicable exclusion zone
by PSOs to assure that no marine mammals are present. The entire
exclusion zone must be visible during the 30-minute lead-in to a full
ramp up. If the entire exclusion zone is not visible, then ramp-up from
a cold start cannot begin. If a marine mammal(s) is sighted within the
injury exclusion zone during the 30-minute watch prior to ramp-up,
ramp-up will be delayed until the marine mammal(s) is sighted outside
of the zone or the animal(s) is not sighted for at least 15-30 minutes:
15 minutes for small odontocetes and pinnipeds (e.g. harbor porpoises,
harbor seals, and Steller sea lions), or 30 minutes for large
odontocetes (e.g., killer whales and beluga whales).
5. Speed or Course Alteration
If a marine mammal is detected outside the injury exclusion zone
and, based on its position and the relative motion, is likely to enter
that zone, the vessel's speed and/or direct course may, when practical
and safe, be changed to avoid the marine mammal and also minimize the
effect on the seismic program. This can be used in coordination with a
power down procedure. The marine mammal activities and movements
relative to the seismic and support vessels will be closely monitored
to ensure that the marine mammal does not approach within the
applicable exclusion radius. If the mammal appears likely to enter the
exclusion radius, further mitigative actions will be taken, i.e.,
either further course alterations, power down, or shut down of the
airgun(s).
6. Measures for Beluga Whales and Groups of Killer Whales and Harbor
Porpoises
The following are additional protective measures for beluga whales
and groups of five or more killer whales and harbor porpoises.
Specifically, a 160-dB vessel monitoring zone will be established and
monitored in Cook Inlet during all seismic surveys. If a beluga whale
or groups of five or more killer whales and/or harbor porpoises are
visually sighted approaching or within the 160-dB disturbance zone,
survey activity will not commence until the animals are no longer
present within the 160-dB disturbance zone. Whenever any beluga whales
or groups of five or more killer whales and/or harbor porpoises are
detected approaching or within the 160-dB disturbance zone, the airguns
may be powered down before the animal is within the 160-dB disturbance
zone, as an alternative to a complete shutdown. If a power down is not
sufficient, the sound source(s) will be shut-down until the animals are
no longer present within the 160-dB zone.
Additional Mitigation Measures Required by NMFS
In addition to the mitigation measures above, NMFS requires
implementation of the following mitigation measures.
SAE will not operate airguns within 10 miles (16 km) of the mean
higher high water (MHHW) line of the Susitna Delta (Beluga River to the
Little Susitna River) between April 15 and October 15. The purpose of
this mitigation measure is to protect beluga whales in the designated
critical habitat in this area that is important for beluga whale
feeding and calving during the spring and fall months. The range of the
setback required by NMFS was designated to protect this important
habitat area and also to create an effective buffer where sound does
not encroach on this habitat. This seasonal exclusion will be in effect
from April 15-October 15. Activities may occur within this area from
October 16-April 14.
A ``mitigation airgun'' (10in\3\) will be operated at approximately
one shot per minute, only during daylight and when there is good
visibility, and will not be operated for longer than 3 hours in
duration. In cases when the next start-up after the turn is expected to
be during lowlight or low visibility, use of the mitigation airgun may
be initiated 30 minutes before darkness or low visibility conditions
occur and may be operated until the start of the next seismic
acquisition line. The mitigation gun must still be operated at
approximately one shot per minute.
When nighttime operations ramp up from the mitigation airgun, SAE
will be required to use passive acoustic monitoring for at least 30
minutes prior to ramp-up to detect beluga whales, humpback whales, and
Steller sea lions that may be within the 160dB disturbance zone. The
support vessel must remain sufficiently distant from the seismic source
vessel to ensure that beluga whales, if present and vocalizing, can be
detected. Passive acoustic monitoring must continue throughout seismic
operations occurring between local sunset and sunrise.
NMFS requires that SAE must suspend seismic operations if a live
marine mammal stranding is reported in Cook Inlet coincident to, or
within 72 hours of, seismic survey activities involving the use of
airguns (regardless of any suspected cause of the stranding). The
shutdown must occur if the animal is within a distance two times that
of the 160 dB isopleth of the largest airgun array configuration in
use. This distance was chosen to create an additional buffer beyond the
distance at which animals would typically be considered harassed, as
animals involved in a live stranding event are likely compromised, with
potentially increased susceptibility to stressors, and the goal is to
decrease the likelihood that they are further disturbed or impacted by
the seismic survey, regardless of what the original cause of the
stranding event was. Shutdown procedures will remain in effect until
NMFS determines and advises SAE that all live animals involved in the
stranding have left the area (either of their own volition or following
herding by responders).
Finally, NMFS requires that if any marine mammal species are
encountered during seismic activities for which take is not authorized,
and are likely to be exposed to sound pressure levels (SPLs) greater
than or equal to 160 dB re 1 [micro]Pa (rms), then SAE must alter speed
or course, power down or shut down the sound source to avoid take of
those species.
Mitigation Conclusions
NMFS has carefully evaluated SAE's mitigation measures and
considered a range of other measures in the context of ensuring that
NMFS prescribes the
[[Page 29180]]
means of aeffecting the least practicable adverse impact on the
affected marine mammal species and stocks and their habitat. Our
evaluation of mitigation 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 measures are 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.
Any mitigation measure(s) prescribed by NMFS should be able to
accomplish, have a reasonable likelihood of accomplishing (based on
current science), or contribute to the accomplishment of one or more of
the general goals listed below:
1. Avoidance or minimization of injury or death of marine mammals
wherever possible (goals 2, 3, and 4 may contribute to this goal).
2. A reduction in the numbers of marine mammals (total number or
number at biologically important time or location) exposed to received
levels of seismic airguns, or other activities expected to result in
the take of marine mammals (this goal may contribute to 1, above, or to
reducing harassment takes only).
3. A reduction in the number of times (total number or number at
biologically important time or location) individuals would be exposed
to received levels of seismic airguns or other activities expected to
result in the take of marine mammals (this goal may contribute to 1,
above, or to reducing harassment takes only).
4. A reduction in the intensity of exposures (either total number
or number at biologically important time or location) to received
levels of seismic airguns or other activities expected to result in the
take of marine mammals (this goal may contribute to 1, above, or to
reducing the severity of harassment takes only).
5. Avoidance or minimization of adverse effects to marine mammal
habitat, paying special attention to the food base, activities that
block or limit passage to or from biologically important areas,
permanent destruction of habitat, or temporary destruction/disturbance
of habitat during a biologically important time.
6. For monitoring directly related to mitigation--an increase in
the probability of detecting marine mammals, thus allowing for more
effective implementation of the mitigation.
Based on our evaluation of the applicant's mitigation measures, as
well as other measures considered by NMFS, NMFS has determined that the
mitigation measures provide the means of effecting the least
practicable adverse impact on marine mammals species or stocks and
their habitat, paying particular attention to rookeries, mating
grounds, and areas of similar significance.
Monitoring and Reporting
Monitoring Measures
1. Visual Vessel-based Monitoring
Vessel-based monitoring for marine mammals will be done by
experienced PSOs throughout the period of marine survey activities.
PSOs will monitor the occurrence and behavior of marine mammals near
the survey vessel during all daylight periods (nautical dawn to
nautical dusk) during operation and during most daylight periods when
airgun operations are not occurring. PSO duties will include watching
for and identifying marine mammals, recording their numbers, distances,
and reactions to the survey operations, and documenting observed ``take
by harassment'' as defined by NMFS.
A minimum number of seven PSOs (two per source vessel and two per
support vessel, with one additional PSO on the mitigation vessel to
operate the hydrophone) will be required onboard the survey vessel to
meet the following criteria: (1) 100 percent monitoring coverage during
all periods of survey operations in daylight (nautical twilight-dawn to
nautical twilight-dusk; (2) maximum of 4 consecutive hours on watch per
PSO; and (3) maximum of 12 hours of watch time per day per PSO.
PSO teams will consist of NMFS-approved field biologists. An
experienced field crew leader will supervise the PSO team onboard the
survey vessel. SAE will have PSOs aboard three vessels: the two source
vessels and one support vessel (M/V Dreamcatcher). Two PSOs will be on
the source vessels, and three PSOs will be on the support vessel to
observe and implement the exclusion, power down, and shut down areas.
When marine mammals are about to enter or are sighted within designated
harassment and exclusion zones, airgun or pinger operations will be
powered down (when applicable) or shut down immediately. The vessel-
based observers will watch for marine mammals during all periods when
sound sources are in operation and for a minimum of 30 minutes prior to
the start of airgun or pinger operations after an extended shut down as
well as 30 minutes after the end of airgun operation.
The observer(s) will watch for marine mammals from the best
available vantage point on the source and support vessels, typically
the flying bridge. The observer(s) will scan systematically with the
unaided eye and 7x50 reticle binoculars, assisted by 40x80 long-range
binoculars.
All observations will be recorded in a standardized format. When a
mammal sighting is made, the following information about the sighting
will be recorded:
Species, group size, age/size/sex categories (if
determinable), sighting cue, behavior when first sighted and after
initial sighting, time of sighting, heading (if consistent), bearing
and distance from the PSO, direction and speed relative to vessel,
apparent reaction to activities (e.g., none, avoidance, approach,
paralleling, etc.), closest point of approach, and behavioral pace;
Time, location, speed, activity of the vessel (e.g.,
seismic airguns off, pingers on, etc.), sea state, ice cover,
visibility, and sun glare; and
The positions of other vessel(s) in the vicinity of the
PSO location.
The ship's position, speed of support vessels, and water
temperature, water depth, sea state, ice cover, visibility, and sun
glare will also be recorded at the start and end of each observation
watch, every 30 minutes during a watch, and whenever there is a change
in any of those variables.
2. Visual Shore-Based Monitoring
In addition to the vessel-based PSOs, SAE will utilize shore-based
monitoring daily in the event of summer seismic activity occurring
nearshore to Cook Inlet beluga Critical Habitat Area 1, to visually
monitor for marine mammals. The shore-based PSOs will scan the area
prior to, during, and after the airgun operations and will be in
contact with the vessel-based PSOs via radio to communicate sightings
of marine mammals approaching or within the project area. This
communication will allow the vessel-based observers to go on a
``heightened'' state of alert regarding occurrence of marine mammals in
the area and aid in timely implementation of mitigation measures.
Reporting Measures
Immediate reports will be submitted to NMFS if 25 belugas are
detected in the Level B disturbance exclusion zone to evaluate and make
necessary adjustments to monitoring and mitigation. If the number of
detected
[[Page 29181]]
takes for any marine mammal species is met or exceeded, SAE will
immediately cease survey operations involving the use of active sound
sources (e.g., airguns and pingers) and notify NMFS.
1. Weekly Reports
SAE will submit a weekly field report to NMFS Headquarters as well
as the Alaska Regional Office, no later than close of business each
Thursday during the weeks when in-water seismic survey activities take
place. The weekly field reports will summarize species detected
(number, location, distance from seismic vessel, behavior), in-water
activity occurring at the time of the sighting (discharge volume of
array at time of sighting, seismic activity at time of sighting, visual
plots of sightings, and number of power downs and shutdowns),
behavioral reactions to in-water activities, and the number of marine
mammals exposed.
2. Monthly Reports
Monthly reports will be submitted to NMFS for all months during
which in-water seismic activities take place. The monthly report will
contain and summarize the following information:
Dates, times, locations, heading, speed, weather, sea
conditions (including Beaufort sea state and wind force), and
associated activities during all seismic operations and marine mammal
sightings.
Species, number, location, distance from the vessel, and
behavior of any sighted marine mammals, as well as associated seismic
activity (number of power-downs and shutdowns), observed throughout all
monitoring activities.
An estimate of the number (by species) of: (i) Pinnipeds
that have been exposed to the seismic activity (based on visual
observation) at received levels greater than or equal to 160 dB re 1
[micro]Pa (rms) and/or 190 dB re 1 [micro]Pa (rms) with a discussion of
any specific behaviors those individuals exhibited; and (ii) cetaceans
that have been exposed to the seismic activity (based on visual
observation) at received levels greater than or equal to 160 dB re 1
[micro]Pa (rms) and/or 180 dB re 1 [micro]Pa (rms) with a discussion of
any specific behaviors those individuals exhibited.
A description of the implementation and effectiveness of
the: (i) Terms and conditions of the Biological Opinion's Incidental
Take Statement (ITS); and (ii) mitigation measures of the IHA. For the
Biological Opinion, the report shall confirm the implementation of each
Term and Condition, as well as any conservation recommendations, and
describe their effectiveness for minimizing the adverse effects of the
action on ESA-listed marine mammals.
3. Annual Reports
SAE will submit an annual report to NMFS's Permits and Conservation
Division within 90 days after the end of operations on the water or at
least 90 days prior to requiring a subsequent authorization, whichever
comes first. The annual report will include:
Summaries of monitoring effort (e.g., total hours, total
distances, and marine mammal distribution through the study period,
accounting for sea state and other factors affecting visibility and
detectability of marine mammals).
Analyses of the effects of various factors influencing
detectability of marine mammals (e.g., sea state, number of observers,
and fog/glare).
Species composition, occurrence, and distribution of
marine mammal sightings, including date, water depth, numbers, age/
size/gender categories (if determinable), group sizes, and ice cover.
Analyses of the effects of survey operations.
Sighting rates of marine mammals during periods with and
without seismic survey activities (and other variables that could
affect detectability), such as: (i) Initial sighting distances versus
survey activity state; (ii) closest point of approach versus survey
activity state; (iii) observed behaviors and types of movements versus
survey activity state; (iv) numbers of sightings/individuals seen
versus survey activity state; (v) distribution around the source
vessels versus survey activity state; and (vi) numbers of animals
detected in the 160 dB harassment (disturbance exclusion) zone.
NMFS will review the draft annual report. SAE must then submit a
final annual report to the Chief, Permits and Conservation Division,
Office of Protected Resources, NMFS, within 30 days after receiving
comments from NMFS on the draft annual report. If NMFS has no comment
on the draft annual report, the draft report shall be considered to be
the final report.
4. Notification of Injured or Dead Marine Mammals
In the unanticipated event that the specified activity clearly
causes the take of a marine mammal in a manner prohibited by this
Authorization, such as an injury (Level A harassment), serious injury
or mortality (e.g., ship-strike, gear interaction, and/or
entanglement), SAE shall immediately cease the specified activities and
immediately report the incident to the Chief of the Permits and
Conservation Division, Office of Protected Resources, NMFS, her
designees, and the Alaska Regional Stranding Coordinators. The report
must include the following information:
Time, date, and location (latitude/longitude) of the
incident;
Name and type of vessel involved;
Vessel's speed during and leading up to the incident;
Description of the incident;
Status of all sound source use in the 24 hours preceding
the incident;
Water depth;
Environmental conditions (e.g., wind speed and direction,
Beaufort sea state, cloud cover, and visibility);
Description of all marine mammal observations in the 24
hours preceding the incident;
Species identification or description of the animal(s)
involved;
Fate of the animal(s); and
Photographs or video footage of the animal(s) (if
equipment is available).
Activities shall not resume until NMFS is able to review the
circumstances of the prohibited take. NMFS shall work with SAE to
determine what is necessary to minimize the likelihood of further
prohibited take and ensure MMPA compliance. SAE may not resume their
activities until notified by NMFS via letter or email, or telephone.
In the event that SAE discovers an injured or dead marine mammal,
and the lead PSO determines that the cause of the injury or death is
unknown and the death is relatively recent (i.e., in less than a
moderate state of decomposition as described in the next paragraph),
SAE will immediately report the incident to the Chief of the Permits
and Conservation Division, Office of Protected Resources, NMFS, her
designees, and the NMFS Alaska Stranding Hotline. The report must
include the same information identified in the paragraph above.
Activities may continue while NMFS reviews the circumstances of the
incident. NMFS will work with SAE to determine whether modifications in
the activities are appropriate.
In the event that SAE discovers an injured or dead marine mammal,
and the lead PSO determines that the injury or death is not associated
with or related to the authorized activities (e.g., previously wounded
animal, carcass with moderate to advanced decomposition, or scavenger
damage), SAE shall report the incident to the Chief of the Permits and
Conservation Division, Office of Protected Resources, NMFS, her
designees, the NMFS Alaska Stranding Hotline, and the Alaska
[[Page 29182]]
Regional Stranding Coordinators within 24 hours of the discovery. SAE
shall provide photographs or video footage (if available) or other
documentation of the stranded animal sighting to NMFS and the Marine
Mammal Stranding Network. Activities may continue while NMFS reviews
the circumstances of the incident.
Monitoring Results From Previously Authorized Activities
While SAE has previously applied for Authorizations for work in
Cook Inlet, Alaska, work was not conducted upon receiving the
Authorization. SAE has previously conducted work under Incidental
Harassment Authorizations in the Beaufort Sea.
Estimated Take by Incidental Harassment
Except with respect to certain activities not pertinent here,
section 3(18) of the MMPA defines ``harassment'' as: Any act of
pursuit, torment, or annoyance which (i) has the potential to injure a
marine mammal or marine mammal stock in the wild; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment]. Only take by Level B behavioral
harassment is anticipated as a result of the seismic survey program
with mitigation measures. Anticipated impacts to marine mammals are
associated with noise propagation from the sound sources (e.g., airguns
and pingers) used in the seismic survey; no take is expected to result
from vessel strikes because of the slow speed of the vessels (4-5
knots).
SAE requests authorization to take nine marine mammal species by
Level B harassment. These nine marine mammal species are: Cook Inlet
beluga whale; humpback whale; minke whale; killer whale; harbor
porpoise; Dall's porpoise; gray whale; harbor seal; and Steller sea
lion.
For impulse sounds, such as those produced by airgun(s) used in the
seismic survey, NMFS uses the 160 dB re 1 [mu]Pa (rms) isopleth to
indicate the onset of Level B harassment. The current Level A (injury)
harassment threshold is 180 dB (rms) for cetaceans and 190 dB (rms) for
pinnipeds. The NMFS annual aerial survey data from 2002-2012 was used
to derive density estimates for each species (number of individuals/
km\2\), and is a large source of the data in the Goetz et al 2012 model
used for beluga density estimation in this Authorization.
Applicable Zones for Estimating ``Take by Harassment''
To estimate potential takes by Level B harassment for this
Authorization, as well as for mitigation radii to be implemented by
PSOs, ranges to the 160 dB (rms), 180 dB, and 190 dB isopleths were
estimated at three different water depths (5 m, 25 m, and 45 m) . The
distances to this threshold for the nearshore survey locations are
provided in Table 4 in SAE's application. The distances to the
thresholds provided in Table 4 in SAE's application correspond to the
broadside and endfire directions.
Compared to the airguns, the relevant isopleths for the positioning
pinger are quite small. The distances to the 190, 180, and 160 dB (rms)
isopleths are 1 m, 3 m, and 25 m (3.3, 10, and 82 ft), respectively.
Estimates of Marine Mammal Density
SAE used one method to estimate densities for Cook Inlet beluga
whales and another method for the other marine mammals in the area
expected to be taken by harassment. Both methods are described in this
document.
1. Beluga Whale Density Estimates
In similar fashion to a previous IHA issued to Apache, SAE used a
habitat-based model developed by Goetz et al. (2012a). Information from
that model has once again been used to estimate densities of beluga
whales in Cook Inlet and we consider it to be the best available
information on beluga density. A summary of the model is provided here,
and additional detail can be found in Goetz et al. (2012a). To develop
NMML's estimated densities of belugas, Goetz et al. (2012a) developed a
model based on aerial survey data, depth soundings, coastal substrate
type, environmental sensitivity index, anthropogenic disturbance, and
anadromous fish streams to predict beluga densities throughout Cook
Inlet. The result of this work is a beluga density map of Cook Inlet,
which easily sums the belugas predicted within a given geographic area.
NMML developed its predictive habitat model from the distribution and
group size of beluga whales observed between 1994 and 2008. A 2-part
``hurdle'' model (a hurdle model in which there are two processes, one
generating the zeroes and one generating the positive values) was
applied to describe the physical and anthropogenic factors that
influence (1) beluga presence (mixed model logistic regression) and (2)
beluga count data (mixed model Poisson regression). Beluga presence was
negatively associated with sources of anthropogenic disturbance and
positively associated with fish availability and access to tidal flats
and sandy substrates. Beluga group size was positively associated with
tidal flats and proxies for seasonally available fish. Using this
analysis, Goetz et al. (2012) produced habitat maps for beluga
presence, group size, and the expected number of belugas in each 1
km\2\ cell of Cook Inlet. The habitat-based model developed by NMML
uses a Geographic Information System (GIS). A GIS is a computer system
capable of capturing, storing, analyzing, and displaying geographically
referenced information; that is, data identified according to location.
However, the Goetz et al. (2012) model does not incorporate seasonality
into the density estimates. Rather, SAE factors in seasonal
considerations of beluga density into the design of the survey
tracklines and locations (as discussion in more detail later in this
document) in addition to other factors such as weather, ice conditions,
and seismic needs.
2. Non-Beluga Whale Species Density Estimates
Densities of other marine mammal species in the project area were
estimated from the annual aerial surveys conducted by NMFS for Cook
Inlet beluga whale between 2000 and 2012 in June (Rugh et al., 2000,
2001, 2002, 2003, 2004b, 2005b, 2006, 2007; Shelden et al., 2008, 2009,
2010, 2012; Hobbs et al., 2011). These surveys were flown in June to
collect abundance data of beluga whales, but sightings of other marine
mammals were also reported. Although these data were only collected in
one month each year, these surveys provide the best available
relatively long term data set for sighting information in the project
area. The general trend in marine mammal sighting is that beluga whales
and harbor seals are the species seen most frequently in upper Cook
Inlet, with concentrations of harbor seals near haul out sites on
Kalgin Island and of beluga whales near river mouths, particularly the
Susitna River. The other marine mammals of interest for this
authorization (humpback whales, gray whales, minke whales, killer
whales, harbor porpoises, Dall's porpoises, Steller sea lions) are
observed infrequently in upper Cook Inlet and more commonly in lower
Cook Inlet. In addition, these densities are calculated based on a
relatively large area that was surveyed, much larger than the proposed
area for a given year of seismic data acquisition. Furthermore, these
annual aerial surveys are conducted only in June (numbers from August
surveys were not used because the area
[[Page 29183]]
surveyed was not provided), so it does not account for seasonal
variations in distribution or habitat use of each species.
Table 5 in SAE's application provides a summary of the results of
NMFS aerial survey data collected in June from 2000 to 2012. To
estimate density of marine mammals, total number of individuals (other
species) observed for the entire survey area by year (surveys usually
last several days) was divided by the approximate total area surveyed
for each year (density = individuals/km\2\). As noted previously, the
total number of animals observed for the entire survey includes both
lower and upper Cook Inlet, so the total number reported and used to
calculate density is higher than the number of marine mammals
anticipated to be observed in the project area. In particular, the
total number of harbor seals observed on several surveys is very high
due to several large haul outs in lower and middle Cook Inlet. The
table below (Table 2) provides average density estimates for gray
whales, harbor seals, harbor porpoises, killer whales, and Steller sea
lions over the 2000-2012 period.
Table 2--Animal Densities in Cook Inlet
------------------------------------------------------------------------
Average density (animals/
Species km\2\)
------------------------------------------------------------------------
Humpback whale............................ 0.0024
Gray whale................................ 9.45E-05
Minke whale............................... 1.14E-05
Killer whale.............................. 0.0008
Dall's porpoise........................... 0.0002
Harbor porpoise........................... 0.0033
Harbor seal............................... 0.28
Steller sea lion.......................... 0.008
------------------------------------------------------------------------
Calculation of Takes by Harassment
1. Beluga Whales
As a result of discussions with NMFS, SAE has used the NMML model
(Goetz et al., 2012a) for the estimate of takes in this Authorization.
SAE has established two zones (Zone 1 and Zone 2) and proposes to
conduct seismic surveys within all, or part of these zones; to be
determined as weather, ice, and priorities dictate, which can be found
in the attached figure which will be posted at https://www.nmfs.noaa.gov/pr/permits/incidental/oilgas.htm
Based on information using Goetz et al. model (2012a), SAE derived
one density estimate for beluga whales in Upper Cook Inlet (i.e., north
of the Forelands) and another density estimate for beluga whales in
Lower Cook Inlet (i.e., south of the Forelands). The density estimate
for Upper Cook Inlet is 0.0212 and is 0.0056 for Lower Cook Inlet.
SAE's seismic operational area will be determined as weather, ice, and
priorities dictate. SAE has requested a maximum allowed take for Cook
Inlet beluga whales of 30 individuals. SAE will operate in a portion of
the total seismic operation area of 3,934 km\2\ (1,519 mi\2\), such
that when one multiplies the anticipated beluga whale density based on
the seismic survey operational area times the area to be ensonified to
the 160-dB isopleth of 9.5 km (5.9 mi) and takes the number of days
into consideration, estimated takes will not exceed 30 beluga whales.
In order to estimate when that level is reached, SAE is using a
formula based on the total potential area of each seismic survey
project zone (including the 160 dB buffer) and the average density of
beluga whales for each zone. Daily take is calculated as the product of
a daily ensonified area times the density in that area. Then daily take
is summed across all the days of the survey until the survey approaches
30 takes.
Table 3--Expected Beluga Whale Takes, Total Area of Zone, and Average Beluga Whale Density Estimates
----------------------------------------------------------------------------------------------------------------
Expected Beluga
takes from NMML Total area of
model (including zone (km2) Average take density (dx)
the 160 dB (including the
buffer) 160 dB buffer)
----------------------------------------------------------------------------------------------------------------
Zone 1--Upper Inlet..................... 28 2,126 d1 = 0.0212
Zone 2--Lower Inlet..................... 29 1,808 d2 = 0.0056
----------------------------------------------------------------------------------------------------------------
SAE will limit surveying in the seismic survey area (Zones 1 and 2
presented in Figures 1 and 2 of SAE's application) to ensure a maximum
of 30 beluga takes during the open water season. In order to ensure
that SAE does not exceed 30 beluga whale takes, the following equation
is being used:
[GRAPHIC] [TIFF OMITTED] TN20MY15.000
This formula also allows SAE to have flexibility to prioritize
survey locations in response to local weather, ice, and operational
constraints. SAE may choose to survey portions of a zone or a zone in
its entirety, and the analysis in this Authorization takes this into
account. Using this formula, if SAE surveys the entire area of Zone 1
(1,319 km\2\), then essentially none of Zone 2 will be surveyed because
the input in the calculation denoted by d2A2 will
essentially need to be zero to ensure that the total allotted take of
beluga whales is not exceeded. The use of this formula will ensure that
SAE's seismic survey will not exceed 30 calculated beluga takes.
Operations are required to cease once SAE has conducted seismic
data acquisition in an area where multiplying the applicable density by
the total ensonified area out to the 160-dB isopleth equaled 30 beluga
whales, using the equation provided above. If 30 belugas are visually
observed before the calculation reaches 30 belugas, SAE is also
required to cease survey activity.
2. Humpback Whales
Although the density for humpback whales in Cook Inlet according to
NMML surveys is 0.0024 animals per km\2\, it is widely known that
humpbacks occur with greater frequency in the lower inlet, and are
rarely sighted in the upper inlet. Apache data has indicated that take
of two humpback whales is possible, but existing observation data of
humpback whales in Cook Inlet
[[Page 29184]]
supports that this is extremely unlikely. No more than two humpback
whales have ever been recorded in a single season by NMFS observers or
PSOs on board seismic vessels in Cook Inlet. Therefore, while the
occurrence of two humpbacks is rare but possible, it is unlikely that
more than five humpbacks will be exposed by Level B harassment based on
known distribution of humpbacks in Cook Inlet.
3. Steller Sea Lions
The density estimate used in the Authorization for Steller sea
lions included NMFS data that includes animals at sea lion haulouts
that are within Cook Inlet, but are well south of the action area. An
anomalous sighting of 20 animals occurred along the southern edge of
the action area, far from any known haulouts or rookeries (such a large
congregation of Steller sea lions far from haulouts or rookeries is
unusual) which is included in NMFS' revised estimate of Steller sea
lion take, but does not include animals observed outside of the action
area. Based on monitoring reports of other seismic activities in Cook
Inlet, there are typically one or two Steller sea lions within the
action area per year. Two individuals were observed by Apache PSOs in
2014 and three groups totaling about four animals were observed in
2012. Because of this data, NMFS has revised its take estimate to 25
individuals, which will account for what one may expect seismic vessels
implementing mitigation measures to encounter in a year, but allows for
the possibility that the survey may encounter an anomalously large
group such as was observed by NMFS aerial observers near the southern
portion of the action area in 2006.
While the NMML survey data reports an average density of 0.008281
Steller sea lions per km\2\ in the action area, NMFS aerial survey data
indicate a maximum density of 0.003518 Steller sea lions per km\2\ with
in the action area (20 animals/5,684 km\2\). Given the size and
location of the action area, we have determined that authorizing take
of 25 Steller sea lions is most appropriate and reflects appropriate
use of the best available scientific data.
4. Harbor seals
As noted above, using the daily ensonified area x number of survey
days x density method results in a reasonable estimate of the instances
of take, but likely significantly overestimates the number of
individual animals expected to be taken. With most species, even this
overestimated number is still very small, and additional analysis is
not really necessary to ensure minor impacts. However, because of the
number and density of harbor seals in the area, a more accurate
understanding of the number of individuals likely taken is necessary to
fully analyze the impacts and ensure that the total number of harbor
seals taken is small.
As described below, we believe that the modeled number of estimated
instances of take referenced above may actually be high, based on
monitoring results from the area. The density estimate from NMFS aerial
surveys includes harbor seal haulouts far south of the action area that
may never move to an ensonified area. Further, we believe that we can
reasonably estimate the comparative number of individual harbor seals
that will likely be taken, based both on monitoring data, operational
information, and an a general understanding of harbor seal habitat use.
Using the daily ensonified area x number of survey days x density
formula (based on surveying 6.7 source lines per day), the number of
instances of exposure above the 160-dB threshold estimated for SAE's
activity in Cook Inlet is 19,315. However, when we examine monitoring
data from previous activities, it is clear this number is an
overestimate--compared to both aerial and vessel based observation
efforts. Apache's monitoring report from 2012 details that they saw
2,474 harbor seals from 29 aerial flights (over 29 days) in the
vicinity of the survey during the month of June, which is the peak
month for harbor seal haulout. In surveying the literature, correction
factors to account for harbor seals in water based on land counts vary
from 1.2 to 1.65 (CITE). Using the most conservative factor of 1.65
(allowing us to consider that some of the other individuals on land may
have entered the water at other points in day), if Apache saw 2,474
seals hauled out then there were an estimated 1,500 seals in the water
during those 29 days. If, because there were only 29 surveys, we
conservatively multiply by 5.5 to estimate the number of seals that
might have been seen if the aerial surveys were conducted for 160 days,
this yields an estimate of 8,250 instances of seal exposure in the
water, which is far less than the estimated 19,315. That the number of
potential instances of exposure is likely less than 19,315 is also
supported by the visual observations from PSOs on board vessels. PSOs
sighted a total of 285 seals in water over 147 days of activity which
would rise to about 310 is adjusted to reflect 160 days of effort.
Given the size of the disturbance zone for these activities, it is
likely that not all harbor seals that were exposed were seen by PSOs,
however 310 is still far less than the estimate of 19,315 given by the
density calculations.
Further, based on the residential nature of harbor seals and the
number of patches SAE plans to shoot, it is possible to reasonably
estimate the number of individual harbor seals exposed, given the
instances of exposures. Based on an estimate of 32 patches in 160 days,
SAE will shoot one patch in 5 days. If seals are generally returning to
haulouts in the survey area over the 5 days of any given patch shoot,
than any given seal in the area could be exposed a minimum of one day
and a maximum of all five days, with an average of 3 days. If the
original exposure estimate using density is 19,315 exposures, then when
divided by three (the average number of times an animal could be
exposed during the shooting of one patch), the expected number of
individuals exposed is 6,438, which is approximately 28% of the
population. This number is also likely an overestimate given that
adjoining patches may be shot, meaning the same seals could be exposed
over multiple patches. Given these multiple methods, as well as the
behavioral preferences of harbor seals for haulouts in certain parts of
the Inlet (Montgomery et al., 2007), and high concentrations at
haulouts in the lower Inlet (Boveng et al.), it is unreasonable to
expect that more than 25% of the population, or 5,725 individuals, will
be taken by Level B harassment during SAE's activity.
5. Other Marine Mammal Species
The estimated takes of other Cook Inlet marine mammals that may be
potentially harassed during the seismic surveys was calculated by
multiplying the following:
Average density estimates (derived from NMFS aerial
surveys from 2000-2012 and presented in Table 3 in this document)
the area ensonified by levels >=160 dB re [mu]Pa rms in
one day (calculated using the total ensonified area per day of 414.92
km\2\, which is derived by applying the buffer distance to the 160 dB
isopleth to the area of 6 survey tracklines),
the number of potential survey days (160).
This equation provides the number of instances of take that will
occur in the duration of the survey, but overestimates the number of
individual animals taken because not every exposure on every successive
day is expected to be a new individual. Especially with resident
species, re-
[[Page 29185]]
exposures of individuals are expected across the months of the survey.
SAE anticipates that a crew will collect seismic data for 8-10
hours per day over approximately 160 days over the course of 8 to 9
months each year. It is assumed that over the course of these 160 days,
no more than 777 km\2\ will be surveyed in total, but areas can be
surveyed more than once. It is important to note that environmental
conditions (such as ice, wind, fog) will play a significant role in the
actual operating days; therefore, these estimates are conservative in
order to provide a basis for probability of encountering these marine
mammal species in the project area.
Summary of Level B Harassment Takes
Table 4 outlines the density estimates used to estimate Level B
harassment takes, the requested Level B harassment take levels, the
abundance of each species in Cook Inlet, the percentage of each species
or stock estimated to be taken, and current population trends.
Table 4--Density Estimates, Level B Harassment Take Levels, Species or Stock Abundance, Percentage of Population
To Be Taken, and Species Trend Status
----------------------------------------------------------------------------------------------------------------
Average density
Species (#individuals/ Level B take Abundance Percentage of Trend
km\2\) population
----------------------------------------------------------------------------------------------------------------
Beluga whale................. Upper=0.0212; 30 312............ 9.6 Decreasing.
Lower=0.0056.
Humpback whale............... 0.0024......... 5 7,469.......... 0.067 Southeast
Alaska
increasing.
Minke whale.................. 1.14E-05....... 1 1,233.......... 0.06 No reliable
information.
Gray whale................... 5.33E-05....... 7 19,126......... 0.033 Stable/
increasing.
Killer whale................. 0.00082........ 55 2,347 2.34 Resident stock
(resident). 15.9 possibly
345 (transient) increasing.
Transient stock
stable.
Harbor porpoise.............. 0.0033......... 219 31,046......... 0.70 No reliable
information.
Dall's porpoise.............. 0.0002......... 14 83,400......... 0.016 No reliable
information.
Harbor seal.................. 0.28........... 5,725 22,900......... 25 Stable.
Steller sea lion............. 0.0082......... 25 45,649......... 0.055 Decreasing but
with regional
variability
(some stable
or
increasing).
----------------------------------------------------------------------------------------------------------------
Analyses and Determinations
Negligible Impact Analysis
Negligible impact is ``an impact resulting from the specified
activity that cannot be reasonably expected to, and is not reasonably
likely to, adversely affect the species or stock through effects on
annual rates of recruitment or survival'' (50 CFR 216.103). A
negligible impact finding is based on the lack of likely adverse
effects on annual rates of recruitment or survival (i.e., population-
level effects). An estimate of the number of 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, feeding, migration,
etc.), as well as the number and nature of estimated Level A harassment
takes, the number of estimated mortalities, effects on habitat, and the
status of the species.
To avoid repetition, the discussion of our analyses applies to all
the species listed in Table 4, divided in some places by group, given
than the anticipated effects of the seismic survey on marine mammals
are expected to be relatively similar in nature. Where there is
information about the size, status, or structure of any species or
stock that would lead to a different analysus (e.g. beluga whales),
species-specific factors have been identified. In some cases however,
we add species-specific information regarding effects (including on
habitat) that also informed our analysis.
Given the required mitigation and related monitoring, no injuries
or mortalities are anticipated to occur as a result of SAE's seismic
survey in Cook Inlet, and none are authorized. Additionally, animals in
the area are not expected to incur hearing impairment (i.e., TTS or
PTS) or non-auditory physiological effects. The number of takes that
are authorized are expected to be limited to short-term Level B
behavioral harassment. The seismic airguns do not operate continuously
over a 24-hour period. Rather airguns are operational for a few hours
at a time totaling about 10 hours a day.
The addition of nine vessels, and noise due to vessel operations
associated with the seismic survey, is not outside the present
experience of marine mammals in Cook Inlet, although levels may
increase locally. Given the large number of vessels in Cook Inlet and
the apparent habituation to vessels by Cook Inlet beluga whales and the
other marine mammals that may occur in the area, vessel activity and
noise is not expected to have effects that could cause significant or
long-term consequences for individual marine mammals or their
populations.
Cook Inlet beluga whales, the western DPS of Steller sea lions, and
Central North Pacific humpback whales are listed as endangered under
the ESA. These stocks are also considered depleted under the MMPA. The
estimated annual rate of decline for Cook Inlet beluga whales was 0.6
percent between 2002 and 2012. Steller sea lion trends for the western
stock are variable throughout the region with some decreasing and
others remaining stable or even indicating slight increases. The
Central North Pacific population of humpbacks is known to be
increasing, with different techniques predicting abundance increases
between 4.9 to 7 percent annually. The other seven species that may be
taken by harassment during SAE's seismic survey program are not listed
as threatened or endangered under the ESA nor as depleted under the
MMPA.
Cetaceans. Odontocete (including Cook Inlet beluga whales, killer
whales, and harbor porpoises) reactions to seismic energy pulses are
usually thought to be limited to shorter distances from the airgun(s)
than are those of mysticetes, in part because odontocete low-frequency
hearing is assumed to be less sensitive than that of mysticetes.
Belugas in the Canadian Beaufort Sea in summer appear to be
[[Page 29186]]
fairly responsive to seismic energy, with few being sighted within 10-
20 km (6-12 mi) of seismic vessels during aerial surveys (Miller et
al., 2005). However, Cook Inlet belugas are more accustomed to
anthropogenic sound than beluga whales in the Beaufort Sea. Therefore,
the results from the Beaufort Sea surveys do not directly translate to
potential reactions of Cook Inlet beluga whales. Also, due to the
dispersed distribution of beluga whales in Cook Inlet during winter and
the concentration of beluga whales in upper Cook Inlet from late April
through early fall, belugas will likely occur in small numbers in the
majority of SAE's survey area during the majority of SAE's annual
operational timeframe of April through December. For the same reason,
as well as mitigation measures, it is unlikely that animals will be
exposed to received levels capable of causing injury.
Potential impacts to marine mammal habitat were discussed
previously in this document (see the ``Anticipated Effects on Habitat''
section). Although some disturbance is possible to food sources of
marine mammals, the impacts are anticipated to be minor enough as to
not affect annual rates of recruitment or survival of marine mammals in
the area. Based on the size of Cook Inlet where feeding by marine
mammals occurs versus the localized area of the marine survey
activities, any missed feeding opportunities in the direct project area
will be minor based on the fact that other feeding areas exist
elsewhere. Taking into account the mitigation measures that are
planned, effects on cetaceans are generally expected to be restricted
to avoidance of a limited area around the survey operation and short-
term changes in behavior, falling within the MMPA definition of ``Level
B harassment''. Animals are not expected to permanently abandon any
area that is surveyed, and any behaviors that are interrupted during
the activity are expected to resume once the activity ceases. Only a
small portion of marine mammal habitat will be affected at any time,
and other areas within Cook Inlet will be available for necessary
biological functions.
In addition, of specific importance to belugas, NMFS seasonally
restricts seismic survey operations in the area known to be important
for beluga whale feeding, calving, or nursing. The primary location for
these biological life functions occurs in the Susitna Delta region of
upper Cook Inlet. NMFS proposes to implement a 16 km (10 mi) seasonal
exclusion from seismic survey operations in this region from April 15-
October 15. The highest concentrations of belugas are typically found
in this area from early May through September each year. NMFS has
incorporated a 2-week buffer on each end of this seasonal use timeframe
to account for any anomalies in distribution and marine mammal usage.
Additionally, in the event that a beluga is seen outside of the
seasonal restricted area and buffer, seismic operations are required to
shut down if a beluga is seen anywhere in the 160dB disturbance zone.
Mitigation measures such as controlled vessel speed, dedicated
marine mammal observers, speed and course alterations, and shutdowns or
power downs when marine mammals are seen within defined ranges designed
both to avoid injury and disturbance will further reduce short-term
reactions and minimize any effects on hearing sensitivity. In all
cases, the effects of the seismic survey are expected to be short-term,
with no lasting biological consequence. Therefore, the exposure of
cetaceans to SAE's seismic survey activity, operation is not
anticipated to have an adverse effect on annual rates of recruitment or
survival of the affected species or stocks of cetaceans, and therefore
will have a negligible impact on them.
Pinnipeds (harbor seals, Steller sea lions). Some individual
pinnipeds may be exposed to sound from the seismic surveys more than
once during the timeframe of the project. Taking into account the
mitigation measures that are planned, effects on pinnipeds are
generally expected to be restricted to avoidance of a limited area
around the survey operation and short-term changes in behavior, falling
within the MMPA definition of ``Level B harassment.'' Animals are not
expected to permanently abandon any area that is surveyed, and any
behaviors that are interrupted during the activity are expected to
resume once the activity ceases. Only a small portion of pinniped
habitat will be affected at any time, and other areas within Cook Inlet
will be available for necessary biological functions. In addition, the
area where the survey will take place is not known to be an important
location where pinnipeds haul out. The closest known haul-out site is
located on Kalgin Island, which is about 22 km from the McArther River.
More recently, some large congregations of harbor seals have been
observed hauling out in upper Cook Inlet. However, mitigation measures,
such as vessel speed, course alteration, and visual monitoring, and
restrictions will be implemented to help reduce impacts to the animals.
Therefore, the exposure of pinnipeds to sounds produced by this phase
of SAE's seismic survey is not anticipated to have an adverse effect on
annual rates of recruitment or survival on those pinniped species or
stocks, and therefore will have a negligible impact.
Based on the analysis contained herein of the likely effects of the
specified activity on marine mammals and their habitat, and taking into
consideration the implementation of the monitoring and mitigation
measures, NMFS finds that SAE's seismic survey will have a negligible
impact on the affected marine mammal species or stocks.
Small Numbers Analysis
The requested takes authorized annually represent 9.6 percent of
the Cook Inlet beluga whale population of approximately 312 animals
(Allen and Angliss, 2014), 2.34 percent of the Alaska resident stock
and 15.9 percent of the Gulf of Alaska, Aleutian Island and Bering Sea
stock of killer whales (1,123 residents and 345 transients), 0.70
percent of the Gulf of Alaska stock of approximately 31,046 harbor
porpoises, 0.067 percent of the 7,469 Central North Pacific humpback
whales, 0.06 percent of the 1,233 Alaska minke whales, 0.016 percent of
the 83,400 Gulf of Alaska Dall's porpoise, and 0.033 percent of the
eastern North Pacific stock of approximately 19,126 gray whales. The
take requests presented for harbor seals represent 25 percent of the
Cook Inlet/Shelikof stock of approximately 22,900 animals. The
requested takes for Steller sea lions represent 0.055 percent of the
U.S. portion of the western stock of approximately 45,649 animals.
These take estimates represent the percentage of each species or stock
that could be taken by Level B behavioral harassment.
NMFS finds that any incidental take reasonably likely to result
from the effects of the activity, as authorized to be mitigated through
this IHA, will be limited to small numbers relative to the affected
species or stocks. In addition to the quantitative methods used to
estimate take, NMFS also considered qualitative factors that further
support the ``small numbers'' determination, including: (1) The
seasonal distribution and habitat use patterns of Cook Inlet beluga
whales, which suggest that for much of the time only a small portion of
the population will be accessible to impacts from SAE's activity, as
most animals are found in the Susitna Delta region of Upper Cook Inlet
from early May through September; (2) other cetacean species and
Steller sea lions are not common in the seismic survey area; (3) the
mitigation requirements, which provide spatio-temporal
[[Page 29187]]
limitations that avoid impacts to large numbers of belugas feeding and
calving in the Susitna Delta and limit exposures to sound levels
associated with Level B harassment; (4) the monitoring requirements and
mitigation measures described earlier in this document for all marine
mammal species that will further reduce the amount of takes; and (5)
monitoring results from previous activities that indicated low numbers
of beluga whale sightings within the Level B disturbance exclusion zone
and low levels of Level B harassment takes of other marine mammals.
Therefore, NMFS determined that the numbers of animals likely to be
taken are small.
Impact on Availability of Affected Species for Taking for Subsistence
Uses
Relevant Subsistence Uses
The subsistence harvest of marine mammals transcends the
nutritional and economic values attributed to the animal and is an
integral part of the cultural identity of the region's Alaska Native
communities. Inedible parts of the whale provide Native artisans with
materials for cultural handicrafts, and the hunting itself perpetuates
Native traditions by transmitting traditional skills and knowledge to
younger generations (NOAA, 2007).
The Cook Inlet beluga whale has traditionally been hunted by Alaska
Natives for subsistence purposes. For several decades prior to the
1980s, the Native Village of Tyonek residents were the primary
subsistence hunters of Cook Inlet beluga whales. During the 1980s and
1990s, Alaska Natives from villages in the western, northwestern, and
North Slope regions of Alaska either moved to or visited the south
central region and participated in the yearly subsistence harvest
(Stanek, 1994). From 1994 to 1998, NMFS estimated 65 whales per year
(range 21-123) were taken in this harvest, including those successfully
taken for food and those struck and lost. NMFS concluded that this
number was high enough to account for the estimated 14 percent annual
decline in the population during this time (Hobbs et al., 2008). Actual
mortality may have been higher, given the difficulty of estimating the
number of whales struck and lost during the hunts. In 1999, a
moratorium was enacted (Pub. L. 106-31) prohibiting the subsistence
take of Cook Inlet beluga whales except through a cooperative agreement
between NMFS and the affected Alaska Native organizations. Since the
Cook Inlet beluga whale harvest was regulated in 1999 requiring
cooperative agreements, five beluga whales have been struck and
harvested. Those beluga whales were harvested in 2001 (one animal),
2002 (one animal), 2003 (one animal), and 2005 (two animals). The
Native Village of Tyonek agreed not to hunt or request a hunt in 2007,
when no co-management agreement was to be signed (NMFS, 2008a).
On October 15, 2008, NMFS published a final rule that established
long-term harvest limits on Cook Inlet beluga whales that may be taken
by Alaska Natives for subsistence purposes (73 FR 60976). That rule
prohibits harvest for a 5-year interval period if the average stock
abundance of Cook Inlet beluga whales over the prior five-year interval
is below 350 whales. Harvest levels for the current 5-year planning
interval (2013-2017) are zero because the average stock abundance for
the previous five-year period (2008-2012) was below 350 whales. Based
on the average abundance over the 2002-2007 period, no hunt occurred
between 2008 and 2012 (NMFS, 2008a). The Cook Inlet Marine Mammal
Council, which managed the Alaska Native Subsistence fishery with NMFS,
was disbanded by a unanimous vote of the Tribes' representatives on
June 20, 2012. At this time, no harvest is expected in 2015 or, likely,
in 2016.
Data on the harvest of other marine mammals in Cook Inlet are
lacking. Some data are available on the subsistence harvest of harbor
seals, harbor porpoises, and killer whales in Alaska in the marine
mammal stock assessments. However, these numbers are for the Gulf of
Alaska including Cook Inlet, and they are not indicative of the harvest
in Cook Inlet.
There is a low level of subsistence hunting for harbor seals in
Cook Inlet. Seal hunting occurs opportunistically among Alaska Natives
who may be fishing or travelling in the upper Inlet near the mouths of
the Susitna River, Beluga River, and Little Susitna River. Some data
are available on the subsistence harvest of harbor seals, harbor
porpoises, and killer whales in Alaska in the marine mammal stock
assessments. However, these numbers are for the Gulf of Alaska
including Cook Inlet, and they are not indicative of the harvest in
Cook Inlet. Some detailed information on the subsistence harvest of
harbor seals is available from past studies conducted by the Alaska
Department of Fish & Game (Wolfe et al., 2009). In 2008, 33 harbor
seals were taken for harvest in the Upper Kenai-Cook Inlet area. In the
same study, reports from hunters stated that harbor seal populations in
the area were increasing (28.6%) or remaining stable (71.4%). The
specific hunting regions identified were Anchorage, Homer, Kenai, and
Tyonek, and hunting generally peaks in March, September, and November
(Wolfe et al., 2009).
Potential Impacts on Availability for Subsistence Uses
Section 101(a)(5)(D) also requires NMFS to determine that the
taking will not have an unmitigable adverse effect on the availability
of marine mammal species or stocks for subsistence use. NMFS has
defined ``unmitigable adverse impact'' in 50 CFR 216.103 as an impact
resulting from the specified activity: (1) That is likely to reduce the
availability of the species to a level insufficient for a harvest to
meet subsistence needs by: (i) Causing the marine mammals to abandon or
avoid hunting areas; (ii) Directly displacing subsistence users; or
(iii) Placing physical barriers between the marine mammals and the
subsistence hunters; and (2) That cannot be sufficiently mitigated by
other measures to increase the availability of marine mammals to allow
subsistence needs to be met.
The primary concern is the disturbance of marine mammals through
the introduction of anthropogenic sound into the marine environment
during the seismic survey. Marine mammals could be behaviorally
harassed and either become more difficult to hunt or temporarily
abandon traditional hunting grounds. The other anthropogenic activities
proposed for Cook Inlet in the 2015 open water season that require an
Authorization are spread throughout the Inlet and not concentrated in
the area of SAE's activity, lessening the concern about spatial
overlap. However, the seismic survey will not have any impacts to
beluga harvests as none currently occur in Cook Inlet. Additionally,
subsistence harvests of other marine mammal species are limited in Cook
Inlet.
Plan of Cooperation or Measures To Minimize Impacts to Subsistence
Hunts
Regulations at 50 CFR 216.104(a)(12) require IHA applicants for
activities that take place in Arctic waters to provide a Plan of
Cooperation or information that identifies what measures have been
taken and/or will be taken to minimize adverse effects on the
availability of marine mammals for subsistence purposes. The entire
upper Cook unit and a portion of the lower Cook unit falls north of
60[deg] N, or within the region NMFS has designated as an Arctic
subsistence use area. There are several villages in SAE's project area
that have traditionally hunted marine mammals, primarily harbor seals.
Tyonek is the only tribal village in upper Cook Inlet with a tradition
of hunting marine
[[Page 29188]]
mammals, in this case harbor seals and beluga whales. However, for
either species the annual recorded harvest since the 1980s has averaged
about one or fewer of either species (Fall et al. 1984, Wolfe et al.
2009, SRBA and HC 2011), and there is currently a moratorium on
subsistence harvest of belugas. Further, many of the seals that are
harvested are done incidentally to salmon fishing or moose hunting
(Fall et al. 1984, Merrill and Orpheim 2013), often near the mouths of
the Susitna Delta rivers (Fall et al. 1984) north of SAE's seismic
survey area.
Villages in lower Cook Inlet adjacent to SAE's seismic area (Kenai,
Salamatof, and Ninilchik) have either not traditionally hunted beluga
whales, or at least not in recent years, and rarely do they harvest sea
lions. Between 1992 and 2008, the only reported sea lion harvests from
this area were two Steller sea lions taken by hunters from Kenai (Wolfe
et al. 2009). These villages more commonly harvest harbor seals, with
Kenai reporting an average of about 13 per year between 1992 and 2008
(Wolfe et al. 2009). According to Fall et al. (1984), many of the seals
harvested by hunters from these villages were taken on the west side of
the inlet during hunting excursions for moose and black bears (or
outside SAE's lower Cook unit). Although marine mammals remain an
important subsistence resource in Cook Inlet, the number of animals
annually harvested are low, and are primarily harbor seals. Much of the
harbor seal harvest occurs incidental to other fishing and hunting
activities, and at areas outside of the SAE's seismic areas such as the
Susitna Delta or the west side of lower Cook Inlet. Also, SAE is
unlikely to conduct seismic activity in the vicinity of any of the
river mouths where large numbers of seals haul out.
SAE has identified the following features that are intended to
reduce impacts to subsistence users:
In-water seismic activities will follow mitigation
procedures to minimize effects on the behavior of marine mammals and,
therefore, opportunities for harvest by Alaska Native communities.
SAE and NMFS recognize the importance of ensuring that ANOs and
federally recognized tribes are informed, engaged, and involved during
the permitting process and will continue to work with the ANOs and
tribes to discuss operations and activities.
From mid-March through April 2015, SAE met with the following
communities and organizations: Nikiski, Ninilchik Native Association
Inc., Tyonek Native Corporation, Tyonek Village, Ninilchik, Nikiski
Facilities Group, and United Cook Inlet Drift Association. These
meetings were meant to inform the audience about the project as well as
listen to concerns and comments. There will also be a review of permit
stipulations and a permit matrix developed for the crews. The means of
communications and contacts list is developed and implemented into the
project, found in SAE's Plan of Cooperation. The use of PSOs/MMO's on
board the vessels will ensure that appropriate precautions are taken to
avoid harassment of marine mammals. If a conflict does occur with
project activities involving subsistence or fishing, the project
manager will immediately contact the affected party to resolve the
conflict. If avoidance is not possible, the project manager will
initiate communication with the Operations Supervisor to resolve the
issue and plan an alternative course of action. The communications will
involve the Permits Manager and the Anchorage Office of SAE.
Unmitigable Adverse Impact Analysis and Determination
The project will not have any effect on beluga whale harvests
because no beluga harvest will take place in 2015. Additionally, the
seismic survey area is not an important native subsistence site for
other subsistence species of marine mammals, and Cook Inlet contains a
relatively small proportion of marine mammals utilizing Cook Inlet;
thus, the number harvested is expected to be extremely low. The timing
and location of subsistence harvest of Cook Inlet harbor seals may
coincide with SAE's project, but because this subsistence hunt is
conducted opportunistically and at such a low level (NMFS, 2013c),
SAE's program is not expected to have an impact on the subsistence use
of harbor seals. Moreover, the survey will result in only temporary
disturbances. Accordingly, the specified activity will not impact the
availability of these other marine mammal species for subsistence uses.
NMFS anticipates that any effects from SAE's seismic survey on
marine mammals, especially harbor seals and Cook Inlet beluga whales,
which are or have been taken for subsistence uses, will be short-term,
site specific, and limited to inconsequential changes in behavior and
mild stress responses. NMFS does not anticipate that the authorized
taking of affected species or stocks will reduce the availability of
the species to a level insufficient for a harvest to meet subsistence
needs by: (1) Causing the marine mammals to abandon or avoid hunting
areas; (2) directly displacing subsistence users; or (3) placing
physical barriers between the marine mammals and the subsistence
hunters; and that cannot be sufficiently mitigated by other measures to
increase the availability of marine mammals to allow subsistence needs
to be met. Based on the description of the specified activity, the
measures described to minimize adverse effects on the availability of
marine mammals for subsistence purposes, and the required mitigation
and monitoring measures, NMFS has determined that there will not be an
unmitigable adverse impact on subsistence uses from SAE's activities.
Endangered Species Act (ESA)
There are three marine mammal species listed as endangered under
the ESA with confirmed or possible occurrence in the project area: The
Cook Inlet beluga whale, the western DPS of Steller sea lion, and the
Central North Pacific humpback whale. In addition, the action could
occur within 10 miles of designated critical habitat for the Cook Inlet
beluga whale. NMFS's Permits and Conservation Division has initiated
consultation with NMFS' Alaska Region Protected Resources Division
under section 7 of the ESA. This consultation concluded on May 7, 2015,
when a Biological Opinion was issued. The Biological Opinion determined
that the issuance of an IHA is not likely to jeapordize the continued
existence of the Cook Inlet beluga whales, Central North Pacific
humpback whales, or western distinct population segment of Steller sea
lions or destroy or adversely modify Cook Inlet beluga whale critical
habitat. Finally, the Alaska region issued an Incidental Take Statement
(ITS) for Cook Inlet beluga whales, humpback whales, and Steller sea
lions. The ITS contains reasonable and prudent measures implemented by
the terms and conditions to minimize the effect of this take.
[[Page 29189]]
National Environmental Policy Act (NEPA)
NMFS prepared an EA that includes an analysis of potential
environmental effects associated with NMFS' issuance of an IHA to SAE
to take marine mammals incidental to conducting a 3D seismic survey
program in Cook Inlet, Alaska. NMFS has finalized the EA and prepared a
FONSI for this action. Therefore, preparation of an Environmental
Impact Statement is not necessary.
Authorization
As a result of these determinations, NMFS has issued an IHA to SAE
for the take of marine mammals incidental to conducting a seismic
survey program in Cook Inlet, Alaska, from May 13, 2015 through May 12,
2016, provided the previously mentioned mitigation, monitoring, and
reporting requirements are incorporated.
Dated: May 12, 2015.
Donna S. Wieting,
Director, Office of Protected Resources, National Marine Fisheries
Service.
[FR Doc. 2015-12091 Filed 5-19-15; 8:45 am]
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