Takes of Marine Mammals Incidental to Specified Activities; Marine Geophysical Survey in the Northwest Pacific Ocean, March Through April 2012, 4765-4787 [2012-2076]
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Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
from the People’s Republic of China, to
no later than February 13, 2012.1
Postponement of Due Date for the
Preliminary Determination
Section 703(b)(1) of the Tariff Act of
1930, as amended (the Act), requires the
Department to issue the preliminary
determination in a countervailing duty
investigation within 65 days after the
date on which the Department initiated
the investigation. However, section
703(c)(1)(A) of the Act permits the
Department to postpone making the
preliminary determination until no later
than 130 days after the date on which
it initiated the investigation if, among
other reasons, the petitioner makes a
timely request for an extension. In the
instant investigation, SolarWorld made
a second timely request on January 19,
2012, for further postponement of the
preliminary countervailing duty
determination by 18 days, to March 2,
2012.2
Therefore, pursuant to the discretion
afforded to the Department under
section 703(c)(1)(A) of the Act, and
because the Department does not find
any compelling reason to deny the
request, we are extending the due date
for the preliminary determination to no
later than March 2, 2012.
This notice is issued and published
pursuant to section 703(c)(2) of the Act
and 19 CFR 351.205(f)(1).
Dated: January 25, 2012.
Paul Piquado,
Assistant Secretary for Import
Administration.
[FR Doc. 2012–2064 Filed 1–30–12; 8:45 am]
BILLING CODE 3510–DS–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XA963
Marine Mammals; File No. 15142
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; receipt of application.
AGENCY:
Notice is hereby given that
Colleen Reichmuth, Ph.D., University of
wreier-aviles on DSK5TPTVN1PROD with NOTICES
SUMMARY:
1 See Crystalline Silicon Photovoltaic Cells,
Whether or Not Assembled Into Modules, From the
People’s Republic of China: Postponement of
Preliminary Determination in the Countervailing
Duty Investigation, 76 FR 81914 (December 29,
2011).
2 See 19 CFR 351.205(e) and the petitioner’s
January 19, 2012 letter requesting a second
postponement of the preliminary determination.
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California at Santa Cruz, Long Marine
Laboratory, 100 Shaffer Road, Santa
Cruz, CA, has applied in due form for
a permit to take bearded seals
(Erignathus barbatus) for research
purposes.
DATES: Written, telefaxed, or email
comments must be received on or before
March 1, 2012.
ADDRESSES: The application and related
documents are available for review by
selecting ‘‘Records Open for Public
Comment’’ from the Features box on the
Applications and Permits for Protected
Species (APPS) home page, https://
apps.nmfs.noaa.gov, and then selecting
File No. 15142 from the list of available
applications.
These documents are also available
upon written request or by appointment
in the following offices:
Permits and Conservation Division,
Office of Protected Resources, NMFS,
1315 East-West Highway, Room 13705,
Silver Spring, MD 20910; phone (301)
427–8401; fax (301) 713–0376;
Alaska Region, NMFS, P.O. Box
21668, Juneau, AK 99802–1668; phone
(907) 586–7221; fax (907) 586–7249; and
Southwest Region, NMFS, 501 West
Ocean Blvd., Suite 4200, Long Beach,
CA 90802–4213; phone (562) 980–4001;
fax (562) 980–4018.
Written comments on this application
should be submitted to the Chief,
Permits and Conservation Division, at
the address listed above. Comments may
also be submitted by facsimile to (301)
713–0376, or by email to
NMFS.Pr1Comments@noaa.gov. Please
include ‘‘File No. 15142’’ in the subject
line of the email comment.
Those individuals requesting a public
hearing should submit a written request
to the Chief, Permits and Conservation
Division at the address listed above. The
request should set forth the specific
reasons why a hearing on this
application would be appropriate.
FOR FURTHER INFORMATION CONTACT:
Amy Sloan or Tammy Adams, (301)
427–8401.
SUPPLEMENTARY INFORMATION: The
subject permit is requested under the
authority of the Marine Mammal
Protection Act of 1972, as amended
(MMPA; 16 U.S.C. 1361 et seq.), and the
regulations governing the taking and
importing of marine mammals (50 CFR
part 216).
The applicant proposes to collect
from the wild up to two bearded seals
in the Northwest Arctic Borough of
Alaska for a long-term behavioral study
at Long Marine Laboratory in Santa
Cruz, CA. Up to four bearded seals may
be captured temporarily in order to
evaluate their suitability for
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4765
participation in research. Captured seals
deemed unsuitable for the long-term
study will be released at the capture
site. Up to two bearded seals deemed
suitable for captive research will be
transported from Kotzebu, AK to Santa
Cruz, CA. Incidental harassment of up
to one ringed seal (Phoca hispida) and
one spotted seal (Phoca larga) may
occur during capture activities.
Authorization for mortality of two
bearded seals is requested for the
duration of the permit. The applicant
requests the permit be valid from
October 1, 2012 to December 31, 2013.
After a quarantine period, the research
to be conducted at Long Marine
Laboratory will occur under existing
NMFS Permit No. 14535–01 (75 FR
58352) and will provide quantitative
measurements of the amphibious
hearing capabilities of bearded seals,
which are needed to improve
understanding of the potential effects of
expected increases in anthropogenic
activities in polar habitats.
In compliance with the National
Environmental Policy Act of 1969
(42 U.S.C. 4321 et seq.), an initial
determination has been made that the
activity proposed is categorically
excluded from the requirement to
prepare an environmental assessment or
environmental impact statement.
Concurrent with the publication of
this notice in the Federal Register,
NMFS is forwarding copies of the
application to the Marine Mammal
Commission and its Committee of
Scientific Advisors.
Dated: January 25, 2012.
P. Michael Payne,
Chief, Permits and Conservation Division,
Office of Protected Resources, National
Marine Fisheries Service.
[FR Doc. 2012–2084 Filed 1–30–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XA879
Takes of Marine Mammals Incidental to
Specified Activities; Marine
Geophysical Survey in the Northwest
Pacific Ocean, March Through April
2012
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; proposed incidental
harassment authorization; request for
comments.
AGENCY:
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Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
NMFS has received an
application from Lamont-Doherty Earth
Observatory (L–DEO), a part of
Columbia University, for an Incidental
Harassment Authorization (IHA) to take
marine mammals, by harassment,
incidental to conducting a marine
geophysical survey in the northwest
Pacific Ocean, March through April,
2012.
SUMMARY:
Comments and information must
be received no later than March 1, 2012.
DATES:
Comments on the
application should be addressed to P.
Michael Payne, Chief, Permits and
Conservation Division, Office of
Protected Resources, National Marine
Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910–
3225. The mailbox address for providing
email comments is ITP.Cody@noaa.gov.
NMFS is not responsible for email
comments sent to addresses other than
the one provided here. Comments sent
via email, including all attachments,
must not exceed a 10-megabyte file size.
All comments received are a part of
the public record and will generally be
posted to https://www.nmfs.noaa.gov/pr/
permits/incidental.htm#applications
without change. All Personal Identifying
Information (for example, name,
address, etc.) voluntarily submitted by
the commenter may be publicly
accessible. Do not submit confidential
business information or otherwise
sensitive or protected information.
An electronic copy of the application
containing a list of the references used
in this document may be obtained by
writing to the above address,
telephoning the contact listed here (see
FOR FURTHER INFORMATION CONTACT) or
visiting the internet at: https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm#applications.
The following associated documents
are also available at the same internet
address: the National Science
Foundation’s (NSF) draft Environmental
Analysis (EA) pursuant to Executive
Order 12114. The EA incorporates an
‘‘Environmental Assessment of a Marine
Geophysical Survey by the R/V Marcus
G. Langseth in the Northwest Pacific
Ocean, March–April, 2012,’’ prepared
by LGL Limited, on behalf of NSF.
Documents cited in this notice may be
viewed, by appointment, during regular
business hours, at the aforementioned
address.
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ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Jeannine Cody, Office of Protected
Resources, NMFS, (301) 427–8401.
SUPPLEMENTARY INFORMATION:
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Background
Section 101(a)(5)(D) of the Marine
Mammal Protection Act of 1972, as
amended (MMPA; 16 U.S.C. 1361 et
seq.) directs the Secretary of Commerce
to authorize, upon request, the
incidental, but not intentional, taking of
small numbers of marine mammals of a
species or population stock, by United
States citizens who engage in a specified
activity (other than commercial fishing)
within a specified geographical region if
certain findings are made and, if the
taking is limited to harassment, a notice
of a proposed authorization is provided
to the public for review.
Authorization for the incidental
taking of small numbers of marine
mammals shall be granted if NMFS
finds that the taking will have a
negligible impact on the species or
stock(s), and will not have an
unmitigable adverse impact on the
availability of the species or stock(s) for
subsistence uses (where relevant). The
authorization must set forth the
permissible methods of taking, other
means of effecting the least practicable
adverse impact on the species or stock
and its habitat, and requirements
pertaining to the mitigation, monitoring
and reporting of such takings. 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.’’
Section 101(a)(5)(D) of the MMPA
established an expedited process by
which citizens of the United States can
apply for an authorization to
incidentally take small numbers of
marine mammals by harassment.
Section 101(a)(5)(D) of the MMPA
establishes a 45-day time limit for
NMFS’ review of an application
followed by a 30-day public notice and
comment period on any proposed
authorizations for the incidental
harassment of small numbers of marine
mammals. Within 45 days of the close
of the public comment period, NMFS
must either issue or deny the
authorization. NMFS must publish a
notice in the Federal Register within
30 days of its determination to issue or
deny the authorization.
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
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disruption of behavioral patterns, including,
but not limited to, migration, breathing,
nursing, breeding, feeding, or sheltering
[Level B harassment].
Summary of Request
NMFS received an application on
October 31, 2011, from L–DEO for the
taking by harassment, of marine
mammals, incidental to conducting a
marine geophysical survey in the
northwest Pacific Ocean in international
waters. Upon receipt of additional
information, NMFS determined the
application complete and adequate on
December 23, 2011.
L–DEO, with research funding from
the U.S. National Science Foundation
(NSF), plans to conduct the survey from
March 24, 2012, through April 16, 2012.
L–DEO received an IHA in 2010 to
conduct the same specified activity in
the same location. However, due to
medical emergencies, L–DEO suspended
its operations and was unable to
complete the seismic survey. Thus, this
2011 survey will allow L–DEO to
acquire data necessary to complete the
abbreviated 2010 study.
L–DEO plans to use one source vessel,
the R/V Marcus G. Langseth (Langseth),
a seismic airgun array and a single
hydrophone streamer to conduct a
geophysical survey at the Shatsky Rise,
a large igneous plateau in the northwest
Pacific Ocean. The proposed survey will
provide data necessary to decipher the
crustal structure of the Shatsky Rise;
may address major questions of earth
history, geodynamics, and tectonics;
could impact the understanding of
terrestrial magmatism and mantle
convection; and may obtain data that
could be used to improve estimates of
regional earthquake occurrence and
distribution. In addition to the
operations of the seismic airgun array
and hydrophone streamer, L–DEO
intends to operate a multibeam
echosounder (MBES) and a sub-bottom
profiler (SBP) continuously throughout
the survey.
Acoustic stimuli (i.e., increased
underwater sound) generated during the
operation of the seismic airgun array,
may have the potential to cause a shortterm behavioral disturbance for marine
mammals in the survey area. This is the
principal means of marine mammal
taking associated with these activities
and L–DEO has requested an
authorization to take 30 species of
marine mammals by Level B
harassment. Take is not expected to
result from the use of the MBES or the
SBP for reasons discussed in this notice.
Also, NMFS does not expect take to
result from collision with the Langseth
because it is a single vessel moving at
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relatively slow speeds (4.6 knots (kts);
8.5 km per hr (km/h); 5.3 miles (mi) per
hour (mph)) during seismic acquisition
within the survey, for a relatively short
period of time. It is likely that any
marine mammal would be able to avoid
the vessel.
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Description of the Specified Activity
L–DEO’s proposed seismic survey on
the Shatsky Rise is scheduled to
commence on March 24, 2012 and end
on April 16, 2012. The Langseth would
depart from Yokohama, Japan on March
24, 2012 and transit to the survey area
in the northwest Pacific Ocean,
approximately 1,200 kilometers (km)
(745.6 miles (mi)) in international
waters offshore of the east coast of
Japan. At the conclusion of the survey
activities, the Langseth proposes to
arrive in Honolulu, Hawaii, on April 16,
2012. Some minor deviation from these
dates is possible, depending on
logistics, weather conditions, and the
need to repeat some lines if data quality
is substandard. Therefore, NMFS
proposes to issue an authorization that
is effective from March 24, 2012 to May
7, 2012.
Geophysical survey activities will
involve 3–D seismic methodologies to
decipher the crustal structure of the
Shatsky Rise. To obtain high-resolution,
2–D structures of the area’s magmatic
systems and thermal structures, the
Langseth will deploy a 36-airgun array
as an energy source and a 6-km-long (3.7
mi-long) hydrophone streamer. As the
airgun array is towed along the survey
lines, the hydrophone streamer will
receive the returning acoustic signals
and transfer the data to the vessel’s onboard processing system.
The proposed study (e.g., equipment
testing, startup, line changes, repeat
coverage of any areas, and equipment
recovery) will require approximately 7
days (d) to complete approximately
1,216 km (755.6 mi) of transect lines.
The Langseth will conduct additional
seismic operations in the survey area
associated with turns, airgun testing,
and repeat coverage of any areas where
the initial data quality is sub-standard.
Data acquisition will include
approximately 168 hours (hr) of airgun
operations (7 d x 24 hr).
L–DEO, the Langseth’s operator, will
conduct all planned seismic data
acquisition activities, with on-board
assistance by the scientists who have
proposed the study. The Principal
Investigators for this survey are Drs. Jun
Korenaga (Yale University, New Haven,
CT) and William Sager (Texas A&M
University, College Station, TX). The
vessel will be self-contained, and the
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crew will live aboard the vessel for the
entire cruise.
Description of the Specified Geographic
Region
L–DEO will conduct the proposed
survey in international waters in the
northwest Pacific Ocean. The study area
will encompass an area on the Shatsky
Rise bounded by approximately 33.5–36
degrees (°) North by 156–161° East (see
Figure 1 in L–DEO’s application). Water
depths in the survey area range from
approximately 3,000 to 5,000 meters (m)
(1.9 to 3.1 mi).
Vessel Specifications
The Langseth, owned by NSF, is a
seismic research vessel with a
propulsion system designed to be as
quiet as possible to avoid interference
with the seismic signals emanating from
the airgun array. The vessel, which has
a length of 71.5 m (235 feet (ft)); a beam
of 17.0 m (56 ft); a maximum draft of 5.9
m (19 ft); and a gross tonnage of 3,834
pounds, is powered by two 3,550
horsepower (hp) Bergen BRG–6 diesel
engines which drive two propellers.
Each propeller has four blades and the
shaft typically rotates at 750 revolutions
per minute. The vessel also has an 800hp bowthruster, which is not used
during seismic acquisition. The
Langseth’s operation speed during
seismic acquisition will be
approximately 4.6 kts (8.5 km/h; 5.3
mph) and the cruising speed of the
vessel outside of seismic operations is
18.5 km/h (11.5 mph or 10 kts).
The Langseth will tow the 36-airgun
array, as well as the hydrophone
streamer, along predetermined lines.
When the Langseth is towing the airgun
array and the hydrophone streamer, the
turning rate of the vessel is limited to
five degrees per minute. Thus, the
maneuverability of the vessel is limited
during operations with the streamer.
The vessel also has an observation
tower from which protected species
visual observers (PSVO) will watch for
marine mammals before and during the
proposed airgun operations. When
stationed on the observation platform,
the PSVO’s eye level will be
approximately 21.5 m (71 ft) above sea
level providing the PSVO an
unobstructed view around the entire
vessel.
Acoustic Source Specifications
Seismic Airguns
The Langseth will deploy a 36-airgun
array, with a total volume of
approximately 6,600 cubic inches (in3)
at a tow depth of 9 m (29.5 ft). The
airguns are a mixture of Bolt 1500LL
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4767
and Bolt 1900LLX airguns ranging in
size from 40 to 360 in3, with a firing
pressure of 1,900 pounds per square
inch. The dominant frequency
components range from zero to 188
Hertz (Hz). The array configuration
consists of four identical linear strings,
with 10 airguns on each string; the first
and last airguns will be spaced 16 m (52
ft) apart. Of the 10 airguns, nine will fire
simultaneously while the tenth airgun
will serve as a spare and will be turned
on in case of failure of one of the other
airguns. The Langseth will distribute the
array across an area of approximately 24
x 16 m (78.7 x 52.5 ft) and will tow the
array approximately 140 m (459.3 ft)
behind the vessel. The tow depth of the
array will be 9 m (29.5 ft).
During the multichannel seismic
(MCS) survey, each airgun array will
emit a pulse at approximately 20-second
(s) intervals which corresponds to a shot
interval of approximately 50 m (164 ft).
During firing, the airguns will emit a
brief (approximately 0.1 s) pulse of
sound; during the intervening periods of
operations, the airguns will be silent.
Metrics Used in This Document
This section includes a brief
explanation of the sound measurements
frequently used in the discussions of
acoustic effects in this document. Sound
pressure is the sound force per unit
area, and is usually measured in
micropascals (mPa), where 1 pascal (Pa)
is the pressure resulting from a force of
one newton exerted over an area of one
square meter. Sound pressure level
(SPL) is expressed as the ratio of a
measured sound pressure and a
reference level. The commonly used
reference pressure level in underwater
acoustics is 1 mPa, and the units for
SPLs are dB re: 1 mPa.
SPL (in decibels (dB)) = 20 log (pressure/
reference pressure)
SPL is an instantaneous measurement
and can be expressed as the peak, the
peak-peak (p-p), or the root mean square
(rms). Root mean square, which is the
square root of the arithmetic average of
the squared instantaneous pressure
values, is typically used in discussions
of the effects of sounds on vertebrates
and all references to SPL in this
document refer to the root mean square
unless otherwise noted. SPL does not
take the duration of a sound into
account.
Characteristics of the Airgun Pulses
Airguns function by venting highpressure air into the water which creates
an air bubble. The pressure signature of
an individual airgun consists of a sharp
rise and then fall in pressure, followed
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by several positive and negative
pressure excursions caused by the
oscillation of the resulting air bubble.
The oscillation of the air bubble
transmits sounds downward through the
seafloor and the amount of sound
transmitted in the near horizontal
directions is reduced. However, the
airgun array also emits sounds that
travel horizontally toward non-target
areas.
The nominal source levels of the
airgun array used by L–DEO on the
Langseth is 236 to 265 dB re: 1 mPa(p-p)
and the rms value for a given airgun
pulse is typically 16 dB re: 1 mPa lower
than the peak-to-peak value (Greene,
1997; McCauley et al., 1998, 2000a).
However, the difference between rms
and peak or peak-to-peak values for a
given pulse depends on the frequency
content and duration of the pulse,
among other factors.
Accordingly, L–DEO has predicted
the received sound levels in relation to
distance and direction from the 36airgun array and the single Bolt 1900LL
40-in3 airgun, which will be used
during power downs. A detailed
description of L–DEO’s modeling for
marine seismic source arrays for species
mitigation is provided in Appendix A of
NSF’s EA. These are the nominal source
levels applicable to downward
propagation. The effective source levels
for horizontal propagation are lower
than those for downward propagation
because of the directional nature of the
sound from the airgun array. Appendix
B(3) of NSF’s EA discusses the
characteristics of the airgun pulses.
NMFS refers the reviewers to the IHA
application and EA documents for
additional information.
Predicted Sound Levels for the Airguns
Tolstoy et al., (2009) reported results
for propagation measurements of pulses
from the Langseth’s 36-airgun, 6,600 in3
array in shallow-water (approximately
50 m (164 ft)) and deep-water depths
(approximately 1,600 m (5,249 ft)) in the
Gulf of Mexico in 2007 and 2008.
Results of the Gulf of Mexico calibration
study (Tolstoy et al., 2009) showed that
radii around the airguns for various
received levels varied with water depth
and that sound propagation varied with
array tow depth.
L–DEO used the results from the Gulf
of Mexico study to determine the
algorithm for its model that calculates
the exclusion zones (EZ) for the 36airgun array and the single airgun. L–
DEO uses these values to designate
mitigation zones and to estimate take
(described in greater detail in Section
VII of L–DEO’s application and Section
IV of NSF’s EA) for marine mammals.
Comparison of the Tolstoy et al.
calibration study with L–DEO’s model
for the Langseth’s 36-airgun array
indicated that the model represents the
actual received levels, within the first
few kilometers, where the predicted EZs
are located. However, the model for
deep water (greater than 1,000 m; 3,280
ft) overestimated the received sound
levels at a given distance but is still
valid for defining exclusion zones at
various tow depths. Because the tow
depth of the array in the calibration
study is less shallow (6 m; 19.7 ft) than
the tow depth array in the proposed
survey (9 m; 29.5 ft), L–DEO used
correction factors for estimating the
received levels in deep water during the
proposed survey. The correction factors
used were the ratios of the 160-,180-,
and 190-dB distances from the modeled
results for the 6,600 in3 airgun array
towed at 6 m (19.7 ft) versus 9 m (29.5
ft) from LGL (2008); 1.285, 1.338, and
1.364 respectively. For a single airgun,
the tow depth has minimal effect on the
maximum near-field output and the
shape of the frequency spectrum for the
single airgun; thus, the predicted EZs
are essentially the same at different tow
depths. The L–DEO model does not
allow for bottom interactions, and thus
is most directly applicable to deep
water.
Table 1 summarizes the predicted
distances at which sound levels (160and 180-dB) are expected to be received
from the 36-airgun array and a single
airgun operating in deep water. To
avoid the potential for injury, NMFS
(1995, 2000) concluded that cetaceans
should not be exposed to pulsed
underwater noise at received levels
exceeding 180 dB re: 1 mPa. NMFS
believes that to avoid the potential for
permanent physiological damage (Level
A harassment), cetaceans should not be
exposed to pulsed underwater noise at
received levels exceeding 180 dB re: 1
mPa. The 180-dB level is a shutdown
criterion applicable to cetaceans, as
specified by NMFS (2000); these levels
were used to establish the EZs. NMFS
also assumes that cetaceans exposed to
levels exceeding 160 dB re: 1 mPa (rms)
may experience Level B harassment.
TABLE 1—MEASURED (ARRAY) OR PREDICTED (SINGLE AIRGUN) DISTANCES TO WHICH SOUND LEVELS GREATER THAN
OR EQUAL TO 160 AND 180 DB RE: 1 μPARms THAT COULD BE RECEIVED IN DEEP WATER USING A 36-AIRGUN
ARRAY, AS WELL AS A SINGLE AIRGUN TOWED AT A DEPTH OF 9 M (29.5 FT) DURING THE PROPOSED SURVEY IN
THE NORTHWEST PACIFIC OCEAN, DURING MARCH–APRIL, 2012
[Distances Are Based On Model Results Provided By L–DEO]
Predicted RMS Distances (m)
Source and volume
Water depth
160 dB
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Single Bolt airgun (40 in3) ...............................................
36–Airgun Array ..............................................................
Appendix A of NSF’s EA discusses L–
DEO’s calculations for the model. NMFS
refers the reviewers to L–DEO’s
application and the NSF’s EA for
additional information.
Multibeam Echosounder
The Langseth will operate a
Kongsberg EM 122 MBES concurrently
during airgun operations to map
characteristics of the ocean floor. The
hull-mounted MBES emits brief pulses
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Deep (>1,000 m) ................
............................................
of sound (also called a ping) (10.5 to 13
kilohertz (kHz)) in a fan-shaped beam
that extends downward and to the sides
of the ship. The transmitting beamwidth
is one or two degrees (°) fore-aft and
150 ° athwartship and the maximum
source level is 242 dB re: 1 mPa.
For deep-water operations, each ping
consists of eight (in water greater than
1,000 m; 3,280 ft) or four (less than
1,000 m; 3,280 ft) successive, fanshaped transmissions, from two to 15
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180 dB
385
3,850
190 dB
40
940
12
400
milliseconds (ms) in duration and each
ensonifying a sector that extends 1 °
fore-aft. Continuous wave pulses
increase from two to 15 milliseconds
(ms) long in water depths up to 2,600 m
(8,530 ft). The MBES uses frequencymodulated chirp pulses up to 100-ms
long in water greater than 2,600 m
(8,530 ft). The eight successive
transmissions span an overall crosstrack angular extent of about 150 °, with
E:\FR\FM\31JAN1.SGM
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2-ms gaps between the pulses for
successive sectors.
Sub-bottom Profiler
The Langseth will also operate a
Knudsen Chirp 3260 SBP concurrently
during airgun and MBES operations to
provide information about the
sedimentary features and bottom
topography. The SBP is capable of
reaching depths of 10,000 m (6.2 mi).
The dominant frequency component of
the SBP is 3.5 kHz which is directed
downward in a 27° cone by a hullmounted transducer on the vessel. The
nominal power output is 10 kilowatts
(kW), but the actual maximum radiated
power is three kW or 222 dB re: 1 mPa.
The ping duration is up to 64 ms with
a pulse interval of one second, but a
common mode of operation is to
broadcast five pulses at 1-s intervals
followed by a 5-s pause.
NMFS expects that acoustic stimuli
resulting from the proposed operation of
the single airgun or the 36-airgun array
has the potential to harass marine
mammals, incidental to the conduct of
the proposed seismic survey. NMFS
expects these disturbances to be
temporary and result in a temporary
robustus) may have the potential to
migrate off of the Pacific coast of Japan
(Reilly et al., 2008a), though any
occurrence in the survey area would be
rare as gray whales are known to prefer
nearshore coastal waters. Based on
available data, L–DEO does not expect
to encounter the western north Pacific
gray whale within the proposed study
area and does not present analysis for
these species. Accordingly, NMFS did
not consider this cetacean species in
Description of the Marine Mammals in
greater detail and the proposed IHA will
the Area of the Specified Activity
only address requested take
Thirty-four marine mammal species
authorizations for the seven mysticetes,
may occur in the Shatsky Rise survey
26 odontocetes, and one species of
area, including 26 odontocetes (toothed
pinniped. The species of marine
cetaceans), seven mysticetes (baleen
mammals expected to be most common
whales) and one species of pinniped
in the survey area (all delphinids)
during March through April. Six of
include the short-beaked common
these species are listed as endangered
(Delphinus delphis), striped (Stenella
under the Endangered Species Act of
coeruleoalba), and Fraser’s
1973 (ESA; 16 U.S.C. 1531 et seq.),
(Lagenodelphis hosei) dolphins, and
including the blue (Balaenoptera
Dall’s porpoise (Phocoenoides dalli).
musculus), fin (Balaenoptera physalus),
Table 2 presents information on the
humpback (Megaptera novaeangliae),
north Pacific right (Eubalaena japonica), abundance, distribution, and
conservation status of the marine
sei (Balaenoptera borealis), and sperm
mammals that may occur in the
(Physeter macrocephalus) whales.
proposed survey area March through
Based on available data, the western
April, 2012.
north Pacific gray whale (Eschrichtius
modification in behavior and/or lowlevel physiological effects (Level B
harassment only) of small numbers of
certain species of marine mammals.
NMFS does not expect that the
movement of the Langseth, during the
conduct of the seismic survey, has the
potential to harass marine mammals
because of the relatively slow operation
speed of the vessel (4.6 kts; 8.5 km/hr;
5.3 mph) during seismic acquisition.
TABLE 2—HABITAT, ABUNDANCE, AND CONSERVATION STATUS OF MARINE MAMMALS THAT MAY OCCUR IN OR NEAR THE
PROPOSED SEISMIC SURVEY AREA ON THE SHATSKY RISE IN THE NORTHWEST PACIFIC OCEAN
[See text and Tables 2 and 3 in L–DEO’s application and the NSF’s EA for further details]
Habitat
Abundance
in the
NW Pacific
Pelagic, coastal ..........................................
Mainly nearshore, banks ............................
Pelagic, coastal ..........................................
Pelagic, coastal ..........................................
Primarily offshore, pelagic ..........................
Continental slope, mostly pelagic ...............
Pelagic, coastal ..........................................
few 100 3 ....................
938–1107 4 ................
25,000 5 .....................
20,501 6 .....................
7260–12,620 7 ...........
13,620–18,680 8 ........
3500 9 ........................
EN
EN
NL
NL
EN
EN
EN
...........
............
............
............
...........
............
............
0.04
0.47
2.51
0.52
1.78
0.74
0.39
Usually pelagic, deep sea ..........................
Deep waters off the shelf ...........................
Deep waters off the shelf ...........................
Pelagic ........................................................
Deep water .................................................
Deep water .................................................
Deep water .................................................
Pelagic ........................................................
Pelagic ........................................................
Deep water .................................................
Deep water .................................................
Coastal, oceanic, shelf break .....................
Pelagic, coastal ..........................................
Pelagic, coastal ..........................................
Off continental shelf ....................................
Waters >1000 m .........................................
Shelf, pelagic, seamounts ..........................
Continental slope, pelagic ..........................
Deep water .................................................
Deep water, seamounts .............................
Oceanic .......................................................
Deep, pantropical waters ............................
Pelagic ........................................................
Widely distributed .......................................
29,674 10 ....................
N.A. ...........................
11,200 11 ....................
20,000 11 ....................
N.A. ...........................
N.A. ...........................
25,300 12 ....................
25,300 12 ....................
25,300 12 ....................
25,300 12 ....................
145,900 11 ..................
168,000 13 ..................
438,000 13 ..................
801,000 14 ..................
570,000 13 ..................
289,300 11 ..................
2,963,000 15 ...............
988,000 16 ..................
307,000 16 ..................
838,000 13 ..................
45,400 11 ....................
38,900 11 ....................
16,000 13 ....................
8500 11 .......................
EN
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
...........
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
............
1.04
3.19
7.82
6.80
0.88
0.45
1.28
0.01
3.12
23.99
70.41
0.83
119.07
4.57
309.35
36.40
0.41
10.8
1.32
0
2.05
0.16
5.00
21.94
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Species
Mysticetes
North Pacific right whale .....................
Humpback whale .................................
Minke whale ........................................
Bryde’s whale ......................................
Sei whale .............................................
Fin whale .............................................
Blue whale ...........................................
Odontocetes
Sperm whale .......................................
Pygmy sperm whale ............................
Dwarf sperm whale .............................
Cuvier’s beaked whale ........................
Baird’s beaked whale ..........................
Longman’s beaked whale ...................
Hubb’s beaked whale ..........................
Ginkgo-toothed beaked whale ............
Blainville’s beaked whale ....................
Stejneger’s beaked whale ...................
Rough-toothed dolphin ........................
Common bottlenose dolphin ...............
Pantropical spotted dolphin .................
Spinner dolphin ...................................
Striped dolphin ....................................
Fraser’s dolphin ...................................
Short-beaked common dolphin ...........
Pacific white-sided dolphin ..................
Northern right whale dolphin ...............
Risso’s dolphin ....................................
Melon-headed whale ...........................
Pygmy killer whale ..............................
False killer whale .................................
Killer whale ..........................................
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Density 2
4770
Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
TABLE 2—HABITAT, ABUNDANCE, AND CONSERVATION STATUS OF MARINE MAMMALS THAT MAY OCCUR IN OR NEAR THE
PROPOSED SEISMIC SURVEY AREA ON THE SHATSKY RISE IN THE NORTHWEST PACIFIC OCEAN—Continued
[See text and Tables 2 and 3 in L–DEO’s application and the NSF’s EA for further details]
Species
Habitat
Abundance
in the
NW Pacific
ESA 1
Short-finned pilot whale .......................
Dall’s porpoise .....................................
Pinnipeds
Northern fur seal .................................
Mostly pelagic, high-relief ...........................
Deep water .................................................
53,000 13 ....................
1,337,224 17 ...............
NL ............
NL ............
1.04
3.19
Pelagic, coastal ..........................................
1.1 million 18 ..............
NL ............
1.79
Density 2
N.A.—Not available or not assessed.
1 Endangered Species Act: EN = Endangered, NL = Not listed
2 Density estimate as listed in Table 3 of L–DEO’s application. Refer to page 41 for specific references.
3 North Pacific (Jefferson et al. 2008).
4 Western North Pacific (Calambokidis et al. 2008).
5 Northwest Pacific and Okhotsk Sea (Buckland et al. 1992; IWC 2010a).
6 Western North Pacific (Kitakado et al. 2008; IWC 2010a).
7 North Pacific (Tillman 1977).
8 North Pacific (Ohsumi and Wada 1974).
9 North Pacific (NMFS 1998).
10 Western North Pacific (Whitehead 2002b).
11 Eastern Tropical Pacific (ETP) (Wade and Gerrodette 1993).
12 ETP; all Mesoplodon spp. (Wade and Gerrodette 1993).
13 Western North Pacific (Miyashita 1993a).
14 Whitebelly spinner dolphin in the ETP in 2000 (Gerrodette et al. 2005 in Hammond et al 2008a).
15 ETP (Gerrodette and Forcada 2002 in Hammond et al 2008b).
16 North Pacific (Miyashita 1993b).
17 North Pacific (Buckland et al 1993).
18 North Pacific, 2004–2005 (Gelatt and Lowry 2008).
NMFS refers the reader to Sections III
and IV of L–DEO’s application for
detailed information regarding the
abundance and distribution, population
status, and life history and behavior of
these species and their occurrence in
the proposed project area. The
application also presents how L–DEO
calculated the estimated densities for
the marine mammals in the proposed
survey area. NMFS has reviewed these
data and determined them to be the best
available scientific information for the
purposes of the proposed IHA.
wreier-aviles on DSK5TPTVN1PROD with NOTICES
Potential Effects on Marine Mammals
Acoustic stimuli generated by the
operation of the airguns, which
introduce sound into the marine
environment, may have the potential to
cause Level B harassment of marine
mammals in the proposed survey area.
The effects of sounds from airgun
operations might include one or more of
the following: tolerance, masking of
natural sounds, behavioral disturbance,
temporary or permanent impairment, or
non-auditory physical or physiological
effects (Richardson et al., 1995; Gordon
et al., 2004; Nowacek et al., 2007;
Southall et al., 2007).
Permanent hearing impairment, in the
unlikely event that it occurred, would
constitute injury, but temporary
threshold shift (TTS) is not an injury
(Southall et al., 2007). Although the
possibility cannot be entirely excluded,
it is unlikely that the proposed project
would result in any cases of temporary
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or permanent hearing impairment, or
any significant non-auditory physical or
physiological effects. Based on the
available data and studies described
here, some behavioral disturbance is
expected, but NMFS expects the
disturbance to be localized and shortterm.
Tolerance
Studies on marine mammals’
tolerance to sound in the natural
environment are relatively rare.
Richardson et al. (1995) defines
tolerance as the occurrence of marine
mammals in areas where they are
exposed to human activities or
manmade noise. In many cases,
tolerance develops by the animal
habituating to the stimulus (i.e., the
gradual waning of responses to a
repeated or ongoing stimulus)
(Richardson, et al., 1995; Thorpe, 1963),
but because of ecological or
physiological requirements, many
marine animals may need to remain in
areas where they are exposed to chronic
stimuli (Richardson, et al., 1995).
Numerous studies have shown that
pulsed sounds from airguns are often
readily detectable in the water at
distances of many kilometers. Several
studies have shown that marine
mammals at distances more than a few
kilometers from operating seismic
vessels often show no apparent response
(see Appendix B(5) in NSF’s EA). That
is often true even in cases when the
pulsed sounds must be readily audible
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to the animals based on measured
received levels and the hearing
sensitivity of the marine mammal group.
Although various baleen whales and
toothed whales, and (less frequently)
pinnipeds have been shown to react
behaviorally to airgun pulses under
some conditions, at other times marine
mammals of all three types have shown
no overt reactions (Stone 2003; Stone
and Tasker 2006; Moulton et al. 2005,
2006a; Weir 2008a for sperm whales),
(MacLean and Koski 2005; Bain and
Williams 2006 for Dall’s porpoises). The
relative responsiveness of baleen and
toothed whales are quite variable.
Masking of Natural Sounds
The term masking refers to the
inability of a subject to recognize the
occurrence of an acoustic stimulus as a
result of the interference of another
acoustic stimulus (Clark et al., 2009).
Introduced underwater sound may,
through masking, reduce the effective
communication distance of a marine
mammal species if the frequency of the
source is close to that used as a signal
by the marine mammal, and if the
anthropogenic sound is present for a
significant fraction of the time
(Richardson et al., 1995).
NMFS expects the masking effects of
pulsed sounds (even from large arrays of
airguns) on marine mammal calls and
other natural sounds to be limited,
although there are very few specific data
on this. Because of the intermittent
nature and low duty cycle of seismic
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airgun pulses, animals can emit and
receive sounds in the relatively quiet
intervals between pulses. However, in
some situations, reverberation occurs for
much or the entire interval between
pulses (e.g., Simard et al., 2005; Clark
and Gagnon, 2006) which could mask
calls. Some baleen and toothed whales
are known to continue calling in the
presence of seismic pulses, and their
calls can usually be heard between the
seismic pulses (e.g., Richardson et al.,
1986; McDonald et al., 1995; Greene et
al., 1999; Nieukirk et al., 2004; Smultea
et al., 2004; Holst et al., 2005a,b, 2006;
and Dunn and Hernandez, 2009).
However, Clark and Gagnon (2006)
reported that fin whales in the northeast
Pacific Ocean went silent for an
extended period starting soon after the
onset of a seismic survey in the area.
Similarly, there has been one report that
sperm whales ceased calling when
exposed to pulses from a very distant
seismic ship (Bowles et al., 1994).
However, more recent studies found
that they continued calling in the
presence of seismic pulses (Madsen et
al., 2002; Tyack et al., 2003; Smultea et
al., 2004; Holst et al., 2006; and Jochens
et al., 2008). Dolphins and porpoises
commonly are heard calling while
airguns are operating (e.g., Gordon et al.,
2004; Smultea et al., 2004; Holst et al.,
2005a, b; and Potter et al., 2007). The
sounds important to small odontocetes
are predominantly at much higher
frequencies than are the dominant
components of airgun sounds, thus
limiting the potential for masking.
In general, NMFS expects the masking
effects of seismic pulses to be minor,
given the normally intermittent nature
of seismic pulses. Refer to Appendix
B(4) of NSF’s EA for a more detailed
discussion of masking effects on marine
mammals.
Behavioral Disturbance
Disturbance includes a variety of
effects, including subtle to conspicuous
changes in behavior, movement, and
displacement. Reactions to sound, if
any, depend on species, state of
maturity, experience, current activity,
reproductive state, time of day, and
many other factors (Richardson et al.,
1995; Wartzok et al., 2004; Southall et
al., 2007; Weilgart, 2007). If a marine
mammal does react briefly to an
underwater sound by changing its
behavior or moving a small distance, the
impacts of the change are unlikely to be
significant to the individual, let alone
the stock or population. However, if a
sound source displaces marine
mammals from an important feeding or
breeding area for a prolonged period,
impacts on individuals and populations
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Jkt 226001
could be significant (e.g., Lusseau and
Bejder, 2007; Weilgart, 2007). Given the
many uncertainties in predicting the
quantity and types of impacts of noise
on marine mammals, it is common
practice to estimate how many
mammals would be present within a
particular distance of industrial
activities and/or exposed to a particular
level of industrial sound. In most cases,
this approach likely overestimates the
numbers of marine mammals that would
be affected in some biologicallyimportant manner.
The sound criteria used to estimate
how many marine mammals might be
disturbed to some biologicallyimportant degree by a seismic program
are based primarily on behavioral
observations of a few species. Scientists
have conducted detailed studies on
humpback, gray, bowhead (Balaena
mysticetus), and sperm whales. Less
detailed data are available for some
other species of baleen whales, small
toothed whales, and sea otters (Enhydra
lutris), but for many species there are no
data on responses to marine seismic
surveys.
Baleen Whales—Baleen whales
generally tend to avoid operating
airguns, but avoidance radii are quite
variable (reviewed in Richardson et al.,
1995). Whales are often reported to
show no overt reactions to pulses from
large arrays of airguns at distances
beyond a few kilometers, even though
the airgun pulses remain well above
ambient noise levels out to much longer
distances. However, as reviewed in
Appendix B(5) of the NSF’s EA, baleen
whales exposed to strong noise pulses
from airguns often react by deviating
from their normal migration route and/
or interrupting their feeding and moving
away from the area. In the cases of
migrating gray and bowhead whales, the
observed changes in behavior appeared
to be of little or no biological
consequence to the animals (Richardson
et al., 1995). They simply avoided the
sound source by displacing their
migration route to varying degrees, but
within the natural boundaries of the
migration corridors.
Studies of gray, bowhead, and
humpback whales have shown that
seismic pulses with received levels of
160 to 170 dB re: 1 mPa seem to cause
obvious avoidance behavior in a
substantial fraction of the animals
exposed (Malme et al., 1986, 1988;
Richardson et al., 1995). In many areas,
seismic pulses from large arrays of
airguns diminish to those levels at
distances ranging from four to 15 km
from the source. A substantial
proportion of the baleen whales within
those distances may show avoidance or
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4771
other strong behavioral reactions to the
airgun array. Subtle behavioral changes
sometimes become evident at somewhat
lower received levels, and studies
summarized in Appendix B(5) of NSF’s
EA have shown that some species of
baleen whales, notably bowhead and
humpback whales, at times show strong
avoidance at received levels lower than
160–170 dB re: 1 mPa.
Researchers have studied the
responses of humpback whales to
seismic surveys during migration,
feeding during the summer months,
breeding while offshore from Angola,
and wintering offshore from Brazil.
McCauley et al. (1998, 2000a) studied
the responses of humpback whales off
western Australia to a full-scale seismic
survey with a 16-airgun array (2,678-in3)
and to a single, 20-in3 airgun with
source level of 227 dB re: 1 mPa (p-p).
In the 1998 study, the researchers
documented that avoidance reactions
began at five to eight km (3.1 to 4.9 mi)
from the array, and that those reactions
kept most pods approximately three to
four km (1.9 to 2.5 mi) from the
operating seismic boat. In the 2000
study, McCauley et al. noted localized
displacement during migration of four
to five km (2.5 to 3.1 mi) by traveling
pods and seven to 12 km (4.3 to 7.5 mi)
by more sensitive resting pods of cowcalf pairs. Avoidance distances with
respect to the single airgun were smaller
but consistent with the results from the
full array in terms of the received sound
levels. The mean received level for
initial avoidance of an approaching
airgun was 140 dB re: 1 mPa for
humpback pods containing females, and
at the mean closest point of approach
distance, the received level was 143 dB
re: 1 mPa. The initial avoidance response
generally occurred at distances of five to
eight km (3.1 to 4.9 mi) from the airgun
array and two km (1.2 mi) from the
single airgun. However, some individual
humpback whales, especially males,
approached within distances of 100 to
400 m (328 to 1,312 ft), where the
maximum received level was 179 dB re:
1 mPa.
Data collected by observers during
several seismic surveys in the northwest
Atlantic Ocean showed that sighting
rates of humpback whales were
significantly greater during non-seismic
periods compared with periods when a
full array was operating (Moulton and
Holst, 2010). In addition, humpback
whales were more likely to swim away
and less likely to swim towards a vessel
during seismic versus non-seismic
periods (Moulton and Holst, 2010).
Humpback whales on their summer
feeding grounds in Frederick Sound and
Stephens Passage, Alaska did not
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Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
exhibit persistent avoidance when
exposed to seismic pulses from a 1.64–
L (100-in3) airgun (Malme et al., 1985).
Some humpbacks seemed ‘‘startled’’ at
received levels of 150 to 169 dB re: 1
mPa. Malme et al. (1985) concluded that
there was no clear evidence of
avoidance, despite the possibility of
subtle effects, at received levels up to
172 re: 1 mPa.
Other studies have suggested that
south Atlantic humpback whales
wintering off Brazil may be displaced or
even strand upon exposure to seismic
surveys (Engel et al., 2004). Although,
the evidence for this was circumstantial
and subject to alternative explanations
(IAGC, 2004). Also, the evidence was
not consistent with subsequent results
from the same area of Brazil (Parente et
al., 2006), or with direct studies of
humpbacks exposed to seismic surveys
in other areas and seasons. After
allowance for data from subsequent
years, there was ‘‘no observable direct
correlation’’ between strandings and
seismic surveys (IWC, 2007: 236).
There are no data on reactions of right
whales to seismic surveys, but results
from the closely-related bowhead whale
show that their responsiveness can be
quite variable depending on their
activity (migrating versus feeding).
Bowhead whales migrating west across
the Alaskan Beaufort Sea in autumn, in
particular, are unusually responsive,
with substantial avoidance occurring
out to distances of 20 to 30 km (12.4 to
18.6 mi) from a medium-sized airgun
source at received sound levels of
approximately 120 to 130 dB re: 1 mPa
(Miller et al., 1999; Richardson et al.,
1999; see Appendix B(5) of NSF’s EA).
However, more recent research on
bowhead whales (Miller et al., 2005;
Harris et al., 2007) corroborates earlier
evidence that, during the summer
feeding season, bowheads are not as
sensitive to seismic sources.
Nonetheless, subtle but statistically
significant changes in surfacing—
respiration—dive cycles were evident
upon statistical analysis (Richardson et
al., 1986). In the summer, bowheads
typically begin to show avoidance
reactions at received levels of about 152
to 178 dB re: 1 mPa (Richardson et al.,
1986, 1995; Ljungblad et al., 1988;
Miller et al., 2005).
Reactions of migrating and feeding
(but not wintering) gray whales to
seismic surveys have been studied.
Malme et al. (1986, 1988) studied the
responses of feeding eastern Pacific gray
whales to pulses from a single 100-in3
airgun off St. Lawrence Island in the
northern Bering Sea. They estimated,
based on small sample sizes, that 50
percent of feeding gray whales stopped
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feeding at an average received pressure
level of 173 dB re: 1 mPa on an
(approximate) rms basis, and that 10
percent of feeding whales interrupted
feeding at received levels of 163 dB re:
1 mPa. Those findings were generally
consistent with the results of
experiments conducted on larger
numbers of gray whales that were
migrating along the California coast
(Malme et al., 1984; Malme and Miles,
1985), and western Pacific gray whales
feeding off Sakhalin Island, Russia
(Wursig et al., 1999; Gailey et al., 2007;
Johnson et al., 2007; Yazvenko et al.,
2007a,b), along with data on gray
whales off British Columbia (Bain and
Williams, 2006).
Various species of Balaenoptera (blue,
sei, fin, and minke whales) have
occasionally been seen in areas
ensonified by airgun pulses (Stone,
2003; MacLean and Haley, 2004; Stone
and Tasker, 2006), and calls from blue
and fin whales have been localized in
areas with airgun operations (e.g.,
McDonald et al., 1995; Dunn and
Hernandez, 2009; Castellote et al.,
2010). Sightings by observers on seismic
vessels off the United Kingdom from
1997 to 2000 suggest that, during times
of good sightability, sighting rates for
mysticetes (mainly fin and sei whales)
were similar when large arrays of
airguns were shooting vs. silent (Stone,
2003; Stone and Tasker, 2006).
However, these whales tended to exhibit
localized avoidance, remaining
significantly further (on average) from
the airgun array during seismic
operations compared with non-seismic
periods (Stone and Tasker, 2006).
Castellote et al. (2010) also observed
localized avoidance by fin whales
during seismic airgun events in the
western Mediterranean Sea and adjacent
Atlantic waters from 2006–2009. They
reported that singing fin whales moved
away from an operating airgun array for
a time period that extended beyond the
duration of the airgun activity.
Ship-based monitoring studies of
baleen whales (including blue, fin, sei,
minke, and whales) in the northwest
Atlantic found that overall, this group
had lower sighting rates during seismic
versus non-seismic periods (Moulton
and Holst, 2010). Baleen whales as a
group were also seen significantly
farther from the vessel during seismic
compared with non-seismic periods,
and they were more often seen to be
swimming away from the operating
seismic vessel (Moulton and Holst,
2010). Blue and minke whales were
initially sighted significantly farther
from the vessel during seismic
operations compared to non-seismic
periods; the same trend was observed
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for fin whales (Moulton and Holst,
2010). Minke whales were most often
observed to be swimming away from the
vessel when seismic operations were
underway (Moulton and Holst, 2010).
Data on short-term reactions by
cetaceans to impulsive noises are not
necessarily indicative of long-term or
biologically significant effects. It is not
known whether impulsive sounds affect
reproductive rate or distribution and
habitat use in subsequent days or years.
However, gray whales have continued to
migrate annually along the west coast of
North America with substantial
increases in the population over recent
years, despite intermittent seismic
exploration (and much ship traffic) in
that area for decades (Appendix A in
Malme et al., 1984; Richardson et al.,
1995; Allen and Angliss, 2011). The
western Pacific gray whale population
did not seem affected by a seismic
survey in its feeding ground during a
previous year (Johnson et al., 2007).
Similarly, bowhead whales have
continued to travel to the eastern
Beaufort Sea each summer, and their
numbers have increased notably,
despite seismic exploration in their
summer and autumn range for many
years (Richardson et al., 1987; Allen and
Agliss, 2011).
Toothed Whales—Little systematic
information is available about reactions
of toothed whales to noise pulses. Few
studies similar to the more extensive
baleen whale/seismic pulse work
summarized earlier and (in more detail)
in Appendix B of NSF’s EA have been
reported for toothed whales. However,
there are recent systematic studies on
sperm whales (e.g., Gordon et al., 2006;
Madsen et al., 2006; Winsor and Mate,
2006; Jochens et al., 2008; Miller et al.,
2009). There is 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; Bain and Williams, 2006;
Holst et al., 2006; Stone and Tasker,
2006; Potter et al., 2007; Hauser et al.,
2008; Holst and Smultea, 2008; Weir,
2008; Barkaszi et al., 2009; Richardson
et al., 2009; Moulton and Holst, 2010).
Seismic operators and protected
species observers (PSOs) on seismic
vessels regularly see dolphins and other
small toothed whales near operating
airgun arrays, but in general there is a
tendency for most delphinids to show
some avoidance of operating seismic
vessels (e.g., Goold, 1996a,b,c;
Calambokidis and Osmek, 1998; Stone,
2003; Moulton and Miller, 2005; Holst
et al., 2006; Stone and Tasker, 2006;
Weir, 2008; Richardson et al., 2009;
Barkaszi et al., 2009; Moulton and
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Holst, 2010). 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 (e.g.,
Moulton and Miller, 2005). Nonetheless,
small toothed whales more often tend to
head away, or to maintain a somewhat
greater distance from the vessel, when a
large array of airguns is operating than
when it is silent (e.g., Stone and Tasker,
2006; Weir, 2008; Barry et al., 2010;
Moulton and Holst, 2010). In most
cases, the avoidance radii for delphinids
appear to be small, on the order of one
km or less, and some individuals show
no apparent avoidance. The beluga
whale (Delphinapterus leucas) is a
species that (at least at times) shows
long-distance avoidance of seismic
vessels. Summer aerial surveys
conducted in the southeastern Beaufort
Sea reported that sighting rates of beluga
whales were significantly lower at
distances of 10 to 20 km (6.2 to 12.4 mi)
from an operating airgun array
compared to distances of 20 to 30 km
(12.4 to 18.6 mi). Further, PSOs on
seismic boats in that area have rarely
reported sighting beluga whales (Miller
et al., 2005; Harris et al., 2007).
Captive bottlenose dolphins (Tursiops
truncatus) and beluga whales exhibited
changes in behavior when exposed to
strong pulsed sounds similar in
duration to those typically used in
seismic surveys (Finneran et al., 2000,
2002, 2005). However, the animals
tolerated high received levels of sound
before exhibiting aversive behaviors.
Results for porpoises depend on
species. The limited available data
suggest that harbor porpoises (Phocoena
phocoena) show stronger avoidance of
seismic operations than do Dall’s
porpoises (Stone, 2003; MacLean and
Koski, 2005; Bain and Williams, 2006;
Stone and Tasker, 2006). Dall’s
porpoises seem relatively tolerant of
airgun operations (MacLean and Koski,
2005; Bain and Williams, 2006),
although they too have been observed to
avoid large arrays of operating airguns
(Calambokidis and Osmek, 1998; Bain
and Williams, 2006). This apparent
difference in responsiveness of these
two porpoise species is consistent with
their relative responsiveness to boat
traffic and some other acoustic sources
(Richardson et al., 1995; Southall et al.,
2007).
Most studies of sperm whales exposed
to airgun sounds indicate that the sperm
whale shows considerable tolerance of
airgun pulses (e.g., Stone, 2003;
Moulton et al., 2005, 2006a; Stone and
Tasker, 2006; Weir, 2008). In most cases
the whales do not show strong
avoidance, and they continue to call
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(see Appendix B of NSF’s EA for
review). However, controlled exposure
experiments in the Gulf of Mexico
indicate that foraging behavior was
altered upon exposure to airgun sound
(Jochens et al., 2008; Miller et al., 2009;
Tyack, 2009).
There are almost no specific data on
the behavioral reactions of beaked
whales to seismic surveys. However,
some northern bottlenose whales
(Hyperoodon ampullatus) remained in
the general area and continued to
produce high-frequency clicks when
exposed to sound pulses from distant
seismic surveys (Gosselin and Lawson,
2004; Laurinolli and Cochrane, 2005;
Simard et al., 2005). Most beaked
whales tend to avoid approaching
vessels of other types (e.g., Wursig et al.,
1998). They may also dive for an
extended period when approached by a
vessel (e.g., Kasuya, 1986), although it is
uncertain how much longer such dives
may be as compared to dives by
undisturbed beaked whales, which also
are often quite long (Baird et al., 2006;
Tyack et al., 2006). Based on a single
observation, Aguilar-Soto et al. (2006)
suggested that foraging efficiency of
Cuvier’s beaked whales (Ziphius
cavirostris) may be reduced by close
approach of vessels. In any event, it is
likely that most beaked whales would
also show strong avoidance of an
approaching seismic vessel, although
this has not been documented
explicitly. In fact, Moulton and Holst
(2010) reported 15 sightings of beaked
whales during seismic studies in the
Northwest Atlantic; seven of those
sightings were made at times when at
least one airgun was operating. There
was little evidence to indicate that
beaked whale behavior was affected by
airgun operations; sighting rates and
distances were similar during seismic
and non-seismic periods (Moulton and
Holst, 2010).
There are increasing indications that
some beaked whales tend to strand
when naval exercises involving midfrequency sonar operation are ongoing
nearby (e.g., Simmonds and LopezJurado, 1991; Frantzis, 1998; NOAA and
USN, 2001; Jepson et al., 2003;
Hildebrand, 2005; Barlow and Gisiner,
2006; see also the Stranding and
Mortality section in this notice). These
strandings are apparently a disturbance
response, although auditory or other
injuries or other physiological effects
may also be involved. Whether beaked
whales would ever react similarly to
seismic surveys is unknown. Seismic
survey sounds are quite different from
those of the sonar in operation during
the above-cited incidents.
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Odontocete reactions to large arrays of
airguns are variable and, at least for
delphinids and Dall’s porpoises, seem to
be confined to a smaller radius than has
been observed for the more responsive
of the mysticetes, belugas, and harbor
porpoises (See Appendix B of NSF’s
EA).
Pinnipeds—Pinnipeds are not likely
to show a strong avoidance reaction to
the airgun array. Visual monitoring from
seismic vessels has shown only slight (if
any) avoidance of airguns by pinnipeds,
and only slight (if any) changes in
behavior, see Appendix B(5) of NSF’s
EA. In the Beaufort Sea, some ringed
seals avoided an area of 100 m (328 ft)
to (at most) a few hundred meters
around seismic vessels, but many seals
remained within 100 to 200 m (328 to
656 ft) of the trackline as the operating
airgun array passed by (e.g., Harris et al.,
2001; Moulton and Lawson, 2002;
Miller et al., 2005). Ringed seal sightings
averaged somewhat farther away from
the seismic vessel when the airguns
were operating than when they were
not, but the difference was small
(Moulton and Lawson, 2002). Similarly,
in Puget Sound, sighting distances for
harbor seals and California sea lions
tended to be larger when airguns were
operating (Calambokidis and Osmek,
1998). Previous telemetry work suggests
that avoidance and other behavioral
reactions may be stronger than evident
to date from visual studies (Thompson
et al., 1998).
Hearing Impairment and Other Physical
Effects
Exposure to high intensity sound for
a sufficient duration may result in
auditory effects such as a noise-induced
threshold shift—an increase in the
auditory threshold after exposure to
noise (Finneran et al., 2005). Factors
that influence the amount of threshold
shift include the amplitude, duration,
frequency content, temporal pattern,
and energy distribution of noise
exposure. The magnitude of hearing
threshold shift normally decreases over
time following cessation of the noise
exposure. The amount of threshold shift
just after exposure is called the initial
threshold shift. If the threshold shift
eventually returns to zero (i.e., the
threshold returns to the pre-exposure
value), it is called temporary threshold
shift (TTS) (Southall et al., 2007).
Researchers have studied TTS in
certain captive odontocetes and
pinnipeds exposed to strong sounds
(reviewed in Southall et al., 2007).
However, there has been no specific
documentation of TTS let alone
permanent hearing damage, i.e.,
permanent threshold shift (PTS), in free-
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ranging marine mammals exposed to
sequences of airgun pulses during
realistic field conditions.
Temporary Threshold Shift—TTS is
the mildest form of hearing impairment
that can occur during exposure to a
strong sound (Kryter, 1985). While
experiencing TTS, the hearing threshold
rises and a sound must be stronger in
order to be heard. At least in terrestrial
mammals, TTS can last from minutes or
hours to (in cases of strong TTS) days.
For sound exposures at or somewhat
above the TTS threshold, hearing
sensitivity in both terrestrial and marine
mammals recovers rapidly after
exposure to the noise ends. Few data on
sound levels and durations necessary to
elicit mild TTS have been obtained for
marine mammals, and none of the
published data concern TTS elicited by
exposure to multiple pulses of sound.
Available data on TTS in marine
mammals are summarized in Southall et
al. (2007). Table 1 (introduced earlier in
this document) presents the distances
from the Langseth’s airguns at which the
received energy level (per pulse, flatweighted) would be expected to be
greater than or equal to 180 dB re: 1 mPa.
To avoid the potential for injury,
NMFS (1995, 2000) concluded that
cetaceans should not be exposed to
pulsed underwater noise at received
levels exceeding 180 dB re: 1 mPa.
NMFS believes that to avoid the
potential for permanent physiological
damage (Level A harassment), cetaceans
should not be exposed to pulsed
underwater noise at received levels
exceeding 180 dB re: 1 mPa. The 180-dB
level is a shutdown criterion applicable
to cetaceans, as specified by NMFS
(2000); these levels were used to
establish the EZs. NMFS also assumes
that cetaceans exposed to SPLs
exceeding 160 dB re: 1 mPa may
experience Level B harassment.
Researchers have derived TTS
information for odontocetes from
studies on the bottlenose dolphin and
beluga. For the one harbor porpoise
tested, the received level of airgun
sound that elicited onset of TTS was
lower (Lucke et al., 2009). If these
results from a single animal are
representative, it is inappropriate to
assume that onset of TTS occurs at
similar received levels in all
odontocetes (cf. Southall et al., 2007).
Some cetaceans apparently can incur
TTS at considerably lower sound
exposures than are necessary to elicit
TTS in the beluga or bottlenose dolphin.
For baleen whales, there are no data,
direct or indirect, on levels or properties
of sound that are required to induce
TTS. The frequencies to which baleen
whales are most sensitive are assumed
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to be lower than those to which
odontocetes are most sensitive, and
natural background noise levels at those
low frequencies tend to be higher. As a
result, auditory thresholds of baleen
whales within their frequency band of
best hearing are believed to be higher
(less sensitive) than are those of
odontocetes at their best frequencies
(Clark and Ellison, 2004). From this, it
is suspected that received levels causing
TTS onset may also be higher in baleen
whales (Southall et al., 2007). For this
proposed study, L–DEO expects no
cases of TTS given the low abundance
of baleen whales in the planned study
area at the time of the survey, and the
strong likelihood that baleen whales
would avoid the approaching airguns
(or vessel) before being exposed to
levels high enough for TTS to occur.
In pinnipeds, TTS thresholds
associated with exposure to brief pulses
(single or multiple) of underwater sound
have not been measured. Initial
evidence from more prolonged
(nonpulse) exposures suggested that
some pinnipeds (harbor seals in
particular) incur TTS at somewhat
lower received levels than do small
odontocetes exposed for similar
durations (Kastak et al., 1999, 2005;
Ketten et al., 2001). The indirectly
estimated TTS threshold for pulsed
sounds would be approximately 181 to
186 dB re: 1 mPa (Southall et al., 2007),
or a series of pulses for which the
highest SEL values are a few dB lower.
Corresponding values for California sea
lions and northern elephant seals are
likely to be higher (Kastak et al., 2005).
Permanent Threshold Shift—When
PTS occurs, there is physical damage to
the sound receptors in the ear. In severe
cases, there can be total or partial
deafness, whereas in other cases, the
animal has an impaired ability to hear
sounds in specific frequency ranges
(Kryter, 1985). There is no specific
evidence that exposure to pulses of
airgun sound can cause PTS in any
marine mammal, even with large arrays
of airguns. However, given the
possibility that mammals close to an
airgun array might incur at least mild
TTS, there has been further speculation
about the possibility that some
individuals occurring very close to
airguns might incur PTS (e.g.,
Richardson et al., 1995, p. 372ff;
Gedamke et al., 2008). Single or
occasional occurrences of mild TTS are
not indicative of permanent auditory
damage, but repeated or (in some cases)
single exposures to a level well above
that causing TTS onset might elicit PTS.
Relationships between TTS and PTS
thresholds have not been studied in
marine mammals, but are assumed to be
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similar to those in humans and other
terrestrial mammals. PTS might occur at
a received sound level at least several
dBs above that inducing mild TTS if the
animal were exposed to strong sound
pulses with rapid rise times–see
Appendix B(6) of NSF’s EA. Based on
data from terrestrial mammals, a
precautionary assumption is that the
PTS threshold for impulse sounds (such
as airgun pulses as received close to the
source) is at least 6 dB higher than the
TTS threshold on a peak-pressure basis,
and probably greater than six dB
(Southall et al., 2007).
Given the higher level of sound
necessary to cause PTS as compared
with TTS, it is considerably less likely
that PTS would occur. Baleen whales
generally avoid the immediate area
around operating seismic vessels, as do
some other marine mammals.
Stranding and Mortality
When a live or dead marine mammal
swims or floats onto shore and becomes
‘‘beached’’ or incapable of returning to
sea, the event is termed a ‘‘stranding’’
(Geraci et al., 1999; Perrin and Geraci,
2002; Geraci and Lounsbury, 2005;
NMFS, 2007). The legal definition for a
stranding under the MMPA is that ‘‘(A)
a marine mammal is dead and is (i) on
a beach or shore of the United States; or
(ii) in waters under the jurisdiction of
the United States (including any
navigable waters); or (B) a marine
mammal is alive and is (i) on a beach
or shore of the United States and is
unable to return to the water; (ii) on a
beach or shore of the United States and,
although able to return to the water, is
in need of apparent medical attention;
or (iii) in the waters under the
jurisdiction of the United States
(including any navigable waters), but is
unable to return to its natural habitat
under its own power or without
assistance’’ (16 U.S.C. 1421h).
Marine mammals are known to strand
for a variety of reasons, such as
infectious agents, biotoxicosis,
starvation, fishery interaction, ship
strike, unusual oceanographic or
weather events, sound exposure, or
combinations of these stressors
sustained concurrently or in series.
However, the cause or causes of most
strandings are unknown (Geraci et al.,
1976; Eaton, 1979; Odell et al., 1980;
Best, 1982). Numerous studies suggest
that the physiology, behavior, habitat
relationships, age, or condition of
cetaceans may cause them to strand or
might predispose them to strand when
exposed to another phenomenon. These
suggestions are consistent with the
conclusions of numerous other studies
that have demonstrated that
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combinations of dissimilar stressors
commonly combine to kill an animal or
dramatically reduce its fitness, even
though one exposure without the other
does not produce the same result
(Chroussos, 2000; Creel, 2005; DeVries
et al., 2003; Fair and Becker, 2000; Foley
et al., 2001; Moberg, 2000; Relyea,
2005a; 2005b, Romero, 2004; Sih et al.,
2004).
Strandings Associated with Military
Active Sonar—Several sources have
published lists of mass stranding events
of cetaceans in an attempt to identify
relationships between those stranding
events and military active sonar
(Hildebrand, 2004; IWC, 2005; Taylor et
al., 2004). For example, based on a
review of stranding records between
1960 and 1995, the International
Whaling Commission (2005) identified
ten mass stranding events and
concluded that, out of eight stranding
events reported from the mid-1980s to
the summer of 2003, seven had been
coincident with the use of midfrequency active sonar and most
involved beaked whales.
Over the past 12 years, there have
been five stranding events coincident
with military MF active sonar use in
which exposure to sonar is believed by
NMFS and the Navy to have been a
contributing factor to strandings: Greece
(1996); the Bahamas (2000); Madeira
(2000); Canary Islands (2002); and Spain
(2006). NMFS refers the reader to Cox et
al. (2006) for a summary of common
features shared by the strandings events
in Greece (1996), Bahamas (2000),
Madeira (2000), and Canary Islands
(2002); and Fernandez et al., (2005) for
an additional summary of the Canary
Islands 2002 stranding event.
Potential for Stranding from Seismic
Surveys—The association of strandings
of beaked whales with naval exercises
involving mid-frequency active sonar
and, in one case, an L–DEO seismic
survey (Malakoff, 2002; Cox et al.,
2006), has raised the possibility that
beaked whales exposed to strong
‘‘pulsed’’ sounds may be especially
susceptible to injury and/or behavioral
reactions that can lead to stranding (e.g.,
Hildebrand, 2005; Southall et al., 2007).
Appendix B (6) of NSF’s EA provides
additional details.
Specific sound-related processes that
lead to strandings and mortality are not
well documented, but may include:
(1) Swimming in avoidance of a
sound into shallow water;
(2) A change in behavior (such as a
change in diving behavior) that might
contribute to tissue damage, gas bubble
formation, hypoxia, cardiac arrhythmia,
hypertensive hemorrhage or other forms
of trauma;
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(3) A physiological change such as a
vestibular response leading to a
behavioral change or stress-induced
hemorrhagic diathesis, leading in turn
to tissue damage; and
(4) Tissue damage directly from sound
exposure, such as through acousticallymediated bubble formation and growth
or acoustic resonance of tissues. Some
of these mechanisms are unlikely to
apply in the case of impulse sounds.
However, there are increasing
indications that gas-bubble disease
(analogous to the bends), induced in
supersaturated tissue by a behavioral
response to acoustic exposure, could be
a pathologic mechanism for the
strandings and mortality of some deepdiving cetaceans exposed to sonar.
However, the evidence for this remains
circumstantial and associated with
exposure to naval mid-frequency sonar,
not seismic surveys (Cox et al., 2006;
Southall et al., 2007).
Seismic pulses and mid-frequency
sonar signals are quite different, and
some mechanisms by which sonar
sounds have been hypothesized to affect
beaked whales are unlikely to apply to
airgun pulses. Sounds produced by
airgun arrays are broadband impulses
with most of the energy below one kHz.
Typical military mid-frequency sonar
emits non-impulse sounds at
frequencies of two to 10 kHz, generally
with a relatively narrow bandwidth at
any one time. A further difference
between seismic surveys and naval
exercises is that naval exercises can
involve sound sources on more than one
vessel. Thus, it is not appropriate to
assume that there is a direct connection
between the effects of military sonar and
seismic surveys on marine mammals.
However, evidence that sonar signals
can, in special circumstances, lead (at
least indirectly) to physical damage and
mortality (e.g., Balcomb and Claridge,
2001; NOAA and USN, 2001; Jepson et
´
al., 2003; Fernandez et al., 2004, 2005;
Hildebrand 2005; Cox et al., 2006)
suggests that caution is warranted when
dealing with exposure of marine
mammals to any high-intensity
‘‘pulsed’’ sound.
There is no conclusive evidence of
cetacean strandings or deaths at sea as
a result of exposure to seismic surveys,
but a few cases of strandings in the
general area where a seismic survey was
ongoing have led to speculation
concerning a possible link between
seismic surveys and strandings.
Suggestions that there was a link
between seismic surveys and strandings
of humpback whales in Brazil (Engel et
al., 2004) were not well founded (IAGC,
2004; IWC, 2007). In September 2002,
there was a stranding of two Cuvier’s
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4775
beaked whales in the Gulf of California,
Mexico, when the L–DEO vessel R/V
Maurice Ewing was operating a 20airgun (8,490 in3) array in the general
area. The link between the stranding
and the seismic surveys was
inconclusive and not based on any
physical evidence (Hogarth, 2002;
Yoder, 2002). Nonetheless, the Gulf of
California incident plus the beaked
whale strandings near naval exercises
involving use of mid-frequency sonar
suggests a need for caution in
conducting seismic surveys in areas
occupied by beaked whales until more
is known about effects of seismic
surveys on those species (Hildebrand,
2005). No injuries of beaked whales are
anticipated during the proposed study
because of:
(1) The likelihood that any beaked
whales nearby would avoid the
approaching vessel before being
exposed to high sound levels; and
(2) Differences between the sound
sources operated by L–DEO and those
involved in the naval exercises
associated with strandings.
Non-Auditory Physiological Effects
Non-auditory physiological effects or
injuries that theoretically might occur in
marine mammals exposed to strong
underwater sound include stress,
neurological effects, bubble formation,
resonance, and other types of organ or
tissue damage (Cox et al., 2006; Southall
et al., 2007). Studies examining such
effects are limited. However, resonance
effects (Gentry, 2002) and direct noiseinduced 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 deepdiving species, this might perhaps 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.
In general, very little is known about
the potential for seismic survey sounds
(or other types of strong 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 nonauditory 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.
Marine mammals that show behavioral
avoidance of seismic vessels, including
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most baleen whales and some
odontocetes, are especially unlikely to
incur non-auditory physical effects.
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Potential Effects of Other Acoustic
Devices
MBES
L–DEO will operate the Kongsberg EM
122 MBES from the source vessel during
the planned study. Sounds from the
MBES are very short pulses, occurring
for two to 15 ms once every five to 20
s, depending on water depth. Most of
the energy in the sound pulses emitted
by this MBES is at frequencies near 12
kHz, and the maximum source level is
242 dB re: 1 mPa. The beam is narrow
(1 to 2°) in fore-aft extent and wide
(150°) in the cross-track extent. Each
ping consists of eight (in water greater
than 1,000 m deep) or four (less than
1,000 m deep) successive fan-shaped
transmissions (segments) at different
cross-track angles. Any given mammal
at depth near the trackline would be in
the main beam for only one or two of
the segments. Also, marine mammals
that encounter the Kongsberg EM 122
are unlikely to be subjected to repeated
pulses because of the narrow fore-aft
width of the beam and will receive only
limited amounts of pulse energy
because of the short pulses. Animals
close to the vessel (where the beam is
narrowest) are especially unlikely to be
ensonified for more than one 2- to 15ms pulse (or two pulses if in the overlap
area). Similarly, Kremser et al. (2005)
noted that the probability of a cetacean
swimming through the area of exposure
when an MBES emits a pulse is small.
The animal would have to pass the
transducer at close range and be
swimming at speeds similar to the
vessel in order to receive the multiple
pulses that might result in sufficient
exposure to cause TTS.
Navy sonars that have been linked to
avoidance reactions and stranding of
cetaceans: (1) Generally have longer
pulse duration than the Kongsberg EM
122; and (2) are often directed close to
horizontally versus more downward for
the MBES. The area of possible
influence of the MBES is much
smaller—a narrow band below the
source vessel. Also, the duration of
exposure for a given marine mammal
can be much longer for naval sonar.
During L–DEO’s operations, the
individual pulses will be very short, and
a given mammal would not receive
many of the downward-directed pulses
as the vessel passes by. Possible effects
of an MBES on marine mammals are
outlined in this section.
Masking—Marine mammal
communications will not be masked
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appreciably by the MBES signals given
the low duty cycle of the echosounder
and the brief period when an individual
mammal is likely to be within its beam.
Furthermore, in the case of baleen
whales, the MBES signals (12 kHz) do
not overlap with the predominant
frequencies in the calls, which would
avoid any significant masking.
Behavioral Responses—Behavioral
reactions of free-ranging marine
mammals to sonars, echosounders, and
other sound sources appear to vary by
species and circumstance. Observed
reactions have included silencing and
dispersal by sperm whales (Watkins et
al., 1985), increased vocalizations and
no dispersal by pilot whales
(Globicephala melas) (Rendell and
Gordon, 1999), and the previouslymentioned beachings by beaked whales.
During exposure to a 21 to 25 kHz
‘‘whale-finding’’ sonar with a source
level of 215 dB re: 1 mPa, gray whales
reacted by orienting slightly away from
the source and being deflected from
their course by approximately 200 m
(Frankel, 2005). When a 38-kHz
echosounder and a 150-kHz acoustic
Doppler current profiler were
transmitting during studies in the
eastern Tropical Pacific Ocean, baleen
whales showed no significant responses,
while spotted and spinner dolphins
were detected slightly more often and
beaked whales less often during visual
surveys (Gerrodette and Pettis, 2005).
Captive bottlenose dolphins and a
beluga whale exhibited changes in
behavior when exposed to 1-s tonal
signals at frequencies similar to those
that will be emitted by the MBES used
by L–DEO, and to shorter broadband
pulsed signals. Behavioral changes
typically involved what appeared to be
deliberate attempts to avoid the sound
exposure (Schlundt et al., 2000;
Finneran et al., 2002; Finneran and
Schlundt, 2004). The relevance of those
data to free-ranging odontocetes is
uncertain, and in any case, the test
sounds were quite different in duration
as compared with those from an MBES.
Hearing Impairment and Other
Physical Effects—Given recent stranding
events that have been associated with
the operation of naval sonar, there is
concern that mid-frequency sonar
sounds can cause serious impacts to
marine mammals (see above). However,
the MBES proposed for use by L–DEO
is quite different than sonar used for
navy operations. Pulse duration of the
MBES is very short relative to the naval
sonar. Also, at any given location, an
individual marine mammal would be in
the beam of the MBES for much less
time given the generally downward
orientation of the beam and its narrow
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fore-aft beamwidth; navy sonar often
uses near-horizontally-directed sound.
Those factors would all reduce the
sound energy received from the MBES
rather drastically relative to that from
naval sonar.
Based upon the best available science,
NMFS believes that the brief exposure
of marine mammals to one pulse, or
small numbers of signals, from the
MBES is not likely to result in the
harassment of marine mammals.
SBP
L–DEO will also operate an SBP from
the source vessel during the proposed
survey. Sounds from the SBP are very
short pulses, occurring for one to four
ms once every second. Most of the
energy in the sound pulses emitted by
the SBP is at 3.5 kHz, and the beam is
directed downward. The sub-bottom
profiler on the Langseth has a maximum
source level of 222 dB re: 1 mPa.
Kremser et al. (2005) noted that the
probability of a cetacean swimming
through the area of exposure when a
bottom profiler emits a pulse is small—
even for an SBP more powerful than
that on the Langseth—if the animal was
in the area, it would have to pass the
transducer at close range and in order to
be subjected to sound levels that could
cause TTS.
Masking—Marine mammal
communications will not be masked
appreciably by the SBP signals given the
directionality of the signal and the brief
period when an individual mammal is
likely to be within its beam.
Furthermore, in the case of most baleen
whales, the SBP signals do not overlap
with the predominant frequencies in the
calls, which would avoid significant
masking.
Behavioral Responses—Marine
mammal behavioral reactions to other
pulsed sound sources are discussed
above, and responses to the SBP are
likely to be similar to those for other
pulsed sources if received at the same
levels. However, the pulsed signals from
the SBP are considerably weaker than
those from the MBES. Therefore,
behavioral responses are not expected
unless marine mammals are very close
to the source.
Hearing Impairment and Other
Physical Effects—It is unlikely that the
SBP produces pulse levels strong
enough to cause hearing impairment or
other physical injuries even in an
animal that is (briefly) in a position near
the source. The SBP is usually operated
simultaneously with other higher-power
acoustic sources. Many marine
mammals will move away in response
to the approaching higher-power
sources or the vessel itself before the
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mammals would be close enough for
there to be any possibility of effects
from the less intense sounds from the
SBP. Based upon the best available
science, NMFS believes that the brief
exposure of marine mammals to signals
from the SBP is not likely to result in
the harassment of marine mammals.
Potential Effects of Vessel Movement
and Collisions
Vessel movement in the vicinity of
marine mammals has the potential to
result in either a behavioral response or
a direct physical interaction. Both
scenarios are discussed below this
section.
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Behavioral Responses to Vessel
Movement
There are limited data concerning
marine mammal behavioral responses to
vessel traffic and vessel noise, and a
lack of consensus among scientists with
respect to what these responses mean or
whether they result in short-term or
long-term adverse effects. In those cases
where there is a busy shipping lane or
where there is a large amount of vessel
traffic, marine mammals may
experience acoustic masking
(Hildebrand, 2005) if they are present in
the area (e.g., killer whales in Puget
Sound; Foote et al., 2004; Holt et al.,
2008). In cases where vessels actively
approach marine mammals (e.g., whale
watching or dolphin watching boats),
scientists have documented that animals
exhibit altered behavior such as
increased swimming speed, erratic
movement, and active avoidance
behavior (Bursk, 1983; Acevedo, 1991;
Baker and MacGibbon, 1991; Trites and
Bain, 2000; Williams et al., 2002;
Constantine et al., 2003), reduced blow
interval (Ritcher et al., 2003), disruption
of normal social behaviors (Lusseau,
2003; 2006), and the shift of behavioral
activities which may increase energetic
costs (Constantine et al., 2003; 2004). A
detailed review of marine mammal
reactions to ships and boats is available
in Richardson et al. (1995). For each of
the marine mammal taxonomy groups,
Richardson et al. (1995) provides the
following assessment regarding
reactions to vessel traffic:
Toothed whales: ‘‘In summary,
toothed whales sometimes show no
avoidance reaction to vessels, or even
approach them. However, avoidance can
occur, especially in response to vessels
of types used to chase or hunt the
animals. This may cause temporary
displacement, but we know of no clear
evidence that toothed whales have
abandoned significant parts of their
range because of vessel traffic.’’
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Baleen whales: ‘‘When baleen whales
receive low-level sounds from distant or
stationary vessels, the sounds often
seem to be ignored. Some whales
approach the sources of these sounds.
When vessels approach whales slowly
and non-aggressively, whales often
exhibit slow and inconspicuous
avoidance maneuvers. In response to
strong or rapidly changing vessel noise,
baleen whales often interrupt their
normal behavior and swim rapidly
away. Avoidance is especially strong
when a boat heads directly toward the
whale.’’
Behavioral responses to stimuli are
complex and influenced to varying
degrees by a number of factors, such as
species, behavioral contexts,
geographical regions, source
characteristics (moving or stationary,
speed, direction, etc.), prior experience
of the animal and physical status of the
animal. For example, studies have
shown that beluga whales’ reactions
varied when exposed to vessel noise
and traffic. In some cases, naive beluga
whales exhibited rapid swimming from
ice-breaking vessels up to 80 km (49.7
mi) away, and showed changes in
surfacing, breathing, diving, and group
composition in the Canadian high
Arctic where vessel traffic is rare (Finley
et al., 1990). In other cases, beluga
whales were more tolerant of vessels,
but responded differentially to certain
vessels and operating characteristics by
reducing their calling rates (especially
older animals) in the St. Lawrence River
where vessel traffic is common (Blane
and Jaakson, 1994). In Bristol Bay,
Alaska, beluga whales continued to feed
when surrounded by fishing vessels and
resisted dispersal even when
purposefully harassed (Fish and Vania,
1971).
In reviewing more than 25 years of
whale observation data, Watkins (1986)
concluded that whale reactions to vessel
traffic were ‘‘modified by their previous
experience and current activity:
habituation often occurred rapidly,
attention to other stimuli or
preoccupation with other activities
sometimes overcame their interest or
wariness of stimuli.’’ Watkins noticed
that over the years of exposure to ships
in the Cape Cod area, minke whales
changed from frequent positive interest
(e.g., approaching vessels) to generally
uninterested reactions; fin whales
changed from mostly negative (e.g.,
avoidance) to uninterested reactions;
right whales apparently continued the
same variety of responses (negative,
uninterested, and positive responses)
with little change; and humpbacks
dramatically changed from mixed
responses that were often negative to
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reactions that were often strongly
positive. Watkins (1986) summarized
that ‘‘whales near shore, even in regions
with low vessel traffic, generally have
become less wary of boats and their
noises, and they have appeared to be
less easily disturbed than previously. In
particular locations with intense
shipping and repeated approaches by
boats (such as the whale-watching areas
of Stellwagen Bank), more and more
whales had positive reactions to familiar
vessels, and they also occasionally
approached other boats and yachts in
the same ways.’’
Although the radiated sound from the
Langseth will be audible to marine
mammals over a large distance, it is
unlikely that animals will respond
behaviorally (in a manner that NMFS
would consider MMPA harassment) to
low-level distant shipping noise as the
animals in the area are likely to be
habituated to such noises (Nowacek et
al., 2004). In light of these facts, NMFS
does not expect the Langseth’s
movements to result in Level B
harassment.
Vessel Strike
Ship strikes of cetaceans can cause
major wounds, which may lead to the
death of the animal. An animal at the
surface could be struck directly by a
vessel, a surfacing animal could hit the
bottom of a vessel, or an animal just
below the surface could be cut by a
vessel’s propeller. The severity of
injuries typically depends on the size
and speed of the vessel (Knowlton and
Kraus, 2001; Laist et al., 2001;
Vanderlaan and Taggart, 2007).
The most vulnerable marine mammals
are those that spend extended periods of
time at the surface in order to restore
oxygen levels within their tissues after
deep dives (e.g., the sperm whale). In
addition, some baleen whales, such as
the North Atlantic right whale, seem
generally unresponsive to vessel sound,
making them more susceptible to vessel
collisions (Nowacek et al., 2004). These
species are primarily large, slow moving
whales. Smaller marine mammals (e.g.,
bottlenose dolphin) move quickly
through the water column and are often
seen riding the bow wave of large ships.
Marine mammal responses to vessels
may include avoidance and changes in
dive pattern (NRC, 2003).
An examination of all known ship
strikes from all shipping sources
(civilian and military) indicates vessel
speed is a principal factor in whether a
vessel strike results in death (Knowlton
and Kraus, 2001; Laist et al., 2001;
Jensen and Silber, 2003; Vanderlaan and
Taggart, 2007). In assessing records in
which vessel speed was known, Laist et
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al. (2001) found a direct relationship
between the occurrence of a whale
strike and the speed of the vessel
involved in the collision. The authors
concluded that most deaths occurred
when a vessel was traveling in excess of
14.9 mph (24.1 km/hr; 13 kts).
L–DEO’s proposed operation of one
vessel for the proposed survey is
relatively small in scale compared to the
number of commercial ships transiting
at higher speeds in the same areas on an
annual basis. The probability of vessel
and marine mammal interactions
occurring during proposed survey is
unlikely due to the Langseth’s slow
operational speed, which is typically 4.6
kts (8.5 km/h; 5.3 mph). Outside of
operations, the Langseth’s cruising
speed would be approximately 11.5
mph (18.5 km/h; 10 kts) which is
generally below the speed at which
studies have noted reported increases of
marine mammal injury or death (Laist et
al., 2001).
As a final point, the Langseth has a
number of other advantages for avoiding
ship strikes as compared to most
commercial merchant vessels, including
the following: the Langseth’s bridge
offers good visibility to visually monitor
for marine mammal presence; PSVOs
posted during operations scan the ocean
for marine mammals and must report
visual alerts of marine mammal
presence to crew; and the PSVOs
receive extensive training that covers
the fundamentals of visual observing for
marine mammals and information about
marine mammals and their
identification at sea.
The potential effects to marine
mammals described in this section of
the document do not take into
consideration the proposed monitoring
and mitigation measures described later
in this document (see the ‘‘Proposed
Mitigation’’ and ‘‘Proposed Monitoring
and Reporting’’ sections) which, as
noted are designed to effect the least
practicable adverse impact on affected
marine mammal species and stocks.
Anticipated Effects on Marine Mammal
Habitat
The proposed seismic survey is not
anticipated to have any permanent
impact on habitats used by the marine
mammals in the proposed survey area,
including the food sources they use (i.e.,
fish and invertebrates). Additionally, no
physical damage to any habitat is
anticipated as a result of conducting the
proposed seismic survey. While it is
anticipated that the specified activity
may result in marine mammals avoiding
certain areas due to temporary
ensonification, this impact to habitat is
temporary and reversible and was
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considered in further detail earlier in
this document, as behavioral
modification.
The main impact associated with the
proposed activity will be temporarily
elevated noise levels and the associated
direct effects on marine mammals,
previously discussed in this notice. The
next section discusses the potential
impacts of anthropogenic sound sources
on common marine mammal prey in the
proposed survey area (i.e., fish and
invertebrates).
Anticipated Effects on Fish
One reason for the adoption of airguns
as the standard energy source for marine
seismic surveys is that, unlike
explosives, they have not been
associated with large-scale fish kills.
However, existing information on the
impacts of seismic surveys on marine
fish populations is limited (see
Appendix D of NSF’s EA). There are
three types of potential effects of
exposure to seismic surveys: (1)
Pathological, (2) physiological, and (3)
behavioral. Pathological effects involve
lethal and temporary or permanent sublethal injury. Physiological effects
involve temporary and permanent
primary and secondary stress responses,
such as changes in levels of enzymes
and proteins. Behavioral effects refer to
temporary and (if they occur) permanent
changes in exhibited behavior (e.g.,
startle and avoidance behavior). The
three categories are interrelated in
complex ways. For example, it is
possible that certain physiological and
behavioral changes could potentially
lead to an ultimate pathological effect
on individuals (i.e., mortality).
The specific received sound levels at
which permanent adverse effects to fish
potentially could occur are little studied
and largely unknown. Furthermore, the
available information on the impacts of
seismic surveys on marine fish is from
studies of individuals or portions of a
population; there have been no studies
at the population scale. The studies of
individual fish have often been on caged
fish that were exposed to airgun pulses
in situations not representative of an
actual seismic survey. Thus, available
information provides limited insight on
possible real-world effects at the ocean
or population scale.
Hastings and Popper (2005), Popper
(2009), and Popper and Hastings
(2009a,b) provided recent critical
reviews of the known effects of sound
on fish. The following sections provide
a general synopsis of the available
information on the effects of exposure to
seismic and other anthropogenic sound
as relevant to fish. The information
comprises results from scientific studies
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of varying degrees of rigor plus some
anecdotal information. Some of the data
sources may have serious shortcomings
in methods, analysis, interpretation, and
reproducibility that must be considered
when interpreting their results (see
Hastings and Popper, 2005). Potential
adverse effects of the program’s sound
sources on marine fish are then noted.
Pathological Effects—The potential
for pathological damage to hearing
structures in fish depends on the energy
level of the received sound and the
physiology and hearing capability of the
species in question (see Appendix D of
NSF’s EA). For a given sound to result
in hearing loss, the sound must exceed,
by some substantial amount, the hearing
threshold of the fish for that sound
(Popper, 2005). The consequences of
temporary or permanent hearing loss in
individual fish on a fish population are
unknown; however, they likely depend
on the number of individuals affected
and whether critical behaviors involving
sound (e.g., predator avoidance, prey
capture, orientation and navigation,
reproduction, etc.) are adversely
affected.
Little is known about the mechanisms
and characteristics of damage to fish
that may be inflicted by exposure to
seismic survey sounds. Few data have
been presented in the peer-reviewed
scientific literature. As far as we know,
there are only two papers with proper
experimental methods, controls, and
careful pathological investigation
implicating sounds produced by actual
seismic survey airguns in causing
adverse anatomical effects. One such
study indicated anatomical damage, and
the second indicated TTS in fish
hearing. The anatomical case is
McCauley et al. (2003), who found that
exposure to airgun sound caused
observable anatomical damage to the
auditory maculae of pink snapper
(Pagrus auratus). This damage in the
ears had not been repaired in fish
sacrificed and examined almost two
months after exposure. On the other
hand, Popper et al. (2005) documented
only TTS (as determined by auditory
brainstem response) in two of three fish
species from the Mackenzie River Delta.
This study found that broad whitefish
(Coregonus nasus) exposed to five
airgun shots were not significantly
different from those of controls. During
both studies, the repetitive exposure to
sound was greater than would have
occurred during a typical seismic
survey. However, the substantial lowfrequency energy produced by the
airguns (less than 400 Hz in the study
by McCauley et al. [2003] and less than
approximately 200 Hz in Popper et al.
[2005]) likely did not propagate to the
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fish because the water in the study areas
was very shallow (approximately 9 m in
the former case and less than two m in
the latter). Water depth sets a lower
limit on the lowest sound frequency that
will propagate (the ‘‘cutoff frequency’’)
at about one-quarter wavelength (Urick,
1983; Rogers and Cox, 1988).
Wardle et al. (2001) suggested that in
water, acute injury and death of
organisms exposed to seismic energy
depends primarily on two features of
the sound source: (1) The received peak
pressure, and (2) the time required for
the pressure to rise and decay.
Generally, as received pressure
increases, the period for the pressure to
rise and decay decreases, and the
chance of acute pathological effects
increases. According to Buchanan et al.
(2004), for the types of seismic airguns
and arrays involved with the proposed
program, the pathological (mortality)
zone for fish would be expected to be
within a few meters of the seismic
source. Numerous other studies provide
examples of no fish mortality upon
exposure to seismic sources (Falk and
Lawrence, 1973; Holliday et al., 1987;
La Bella et al., 1996; Santulli et al.,
1999; McCauley et al., 2000a,b, 2003;
Bjarti, 2002; Thomsen, 2002; Hassel et
al., 2003; Popper et al., 2005; Boeger et
al., 2006).
Some studies have reported, some
equivocally, that mortality of fish, fish
eggs, or larvae can occur close to
seismic sources (Kostyuchenko, 1973;
Dalen and Knutsen, 1986; Booman et
al., 1996; Dalen et al., 1996). Some of
the reports claimed seismic effects from
treatments quite different from actual
seismic survey sounds or even
reasonable surrogates. However, Payne
et al. (2009) reported no statistical
differences in mortality/morbidity
between control and exposed groups of
capelin eggs or monkfish larvae. Saetre
and Ona (1996) applied a ‘worst-case
scenario’ mathematical model to
investigate the effects of seismic energy
on fish eggs and larvae. They concluded
that mortality rates caused by exposure
to seismic surveys are so low, as
compared to natural mortality rates, that
the impact of seismic surveying on
recruitment to a fish stock must be
regarded as insignificant.
Physiological Effects—Physiological
effects refer to cellular and/or
biochemical responses of fish to
acoustic stress. Such stress potentially
could affect fish populations by
increasing mortality or reducing
reproductive success. Primary and
secondary stress responses of fish after
exposure to seismic survey sound
appear to be temporary in all studies
done to date (Sverdrup et al., 1994;
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Santulli et al., 1999; McCauley et al.,
2000a,b). The periods necessary for the
biochemical changes to return to normal
are variable and depend on numerous
aspects of the biology of the species and
of the sound stimulus (see Appendix D
of NSF’s EA).
Behavioral Effects—Behavioral effects
include changes in the distribution,
migration, mating, and catchability of
fish populations. Studies investigating
the possible effects of sound (including
seismic survey sound) on fish behavior
have been conducted on both uncaged
and caged individuals (e.g., Chapman
and Hawkins, 1969; Pearson et al., 1992;
Santulli et al., 1999; Wardle et al., 2001;
Hassel et al., 2003). Typically, in these
studies fish exhibited a sharp startle
response at the onset of a sound
followed by habituation and a return to
normal behavior after the sound ceased.
In general, any adverse effects on fish
behavior or fisheries attributable to
seismic testing may depend on the
species in question and the nature of the
fishery (season, duration, fishing
method). They may also depend on the
age of the fish, its motivational state, its
size, and numerous other factors that are
difficult, if not impossible, to quantify at
this point, given such limited data on
effects of airguns on fish, particularly
under realistic at-sea conditions.
Anticipated Effects on Fisheries
It is possible that the Langseth’s
streamer may become entangled with
various types of fishing gear. L–DEO
will employ avoidance tactics as
necessary to prevent conflict. It is not
expected that L–DEO’s operations will
have a significant impact on fisheries in
the western Pacific Ocean. Nonetheless,
L–DEO will minimize the potential to
have a negative impact on the fisheries
by avoiding areas where fishing is
actively underway.
There is general concern about
potential adverse effects of seismic
operations on fisheries, namely a
potential reduction in the ‘‘catchability’’
of fish involved in fisheries. Although
reduced catch rates have been observed
in some marine fisheries during seismic
testing, in a number of cases the
findings are confounded by other
sources of disturbance (Dalen and
Raknes, 1985; Dalen and Knutsen, 1986;
Lokkeborg, 1991; Skalski et al., 1992;
Engas et al., 1996). In other airgun
experiments, there was no change in
catch per unit effort of fish when airgun
pulses were emitted, particularly in the
immediate vicinity of the seismic survey
(Pickett et al., 1994; La Bella et al.,
1996). For some species, reductions in
catch may have resulted from a change
in behavior of the fish, e.g., a change in
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vertical or horizontal distribution, as
reported in Slotte et al. (2004).
Anticipated Effects on Invertebrates
The existing body of information on
the impacts of seismic survey sound on
marine invertebrates is very limited.
However, there is some unpublished
and very limited evidence of the
potential for adverse effects on
invertebrates, thereby justifying further
discussion and analysis of this issue.
The three types of potential effects of
exposure to seismic surveys on marine
invertebrates are pathological,
physiological, and behavioral. Based on
the physical structure of their sensory
organs, marine invertebrates appear to
be specialized to respond to particle
displacement components of an
impinging sound field and not to the
pressure component (Popper et al.,
2001; see also Appendix E of NSF’s EA).
The only information available on the
impacts of seismic surveys on marine
invertebrates involves studies of
individuals; there have been no studies
at the population scale. Thus, available
information provides limited insight on
possible real-world effects at the
regional or ocean scale. The most
important aspect of potential impacts
concerns how exposure to seismic
survey sound ultimately affects
invertebrate populations and their
viability, including availability to
fisheries.
Literature reviews of the effects of
seismic and other underwater sound on
invertebrates were provided by
Moriyasu et al. (2004) and Payne et al.
(2008). The following sections provide a
synopsis of available information on the
effects of exposure to seismic survey
sound on species of decapod
crustaceans and cephalopods, the two
taxonomic groups of invertebrates on
which most such studies have been
conducted. The available information is
from studies with variable degrees of
scientific soundness and from anecdotal
information. A more detailed review of
the literature on the effects of seismic
survey sound on invertebrates is
provided in Appendix E of L–DEO’s EA.
Pathological Effects—In water, lethal
and sub-lethal injury to organisms
exposed to seismic survey sound
appears to depend on at least two
features of the sound source: (1) The
received peak pressure; and (2) the time
required for the pressure to rise and
decay. Generally, as received pressure
increases, the period for the pressure to
rise and decay decreases, and the
chance of acute pathological effects
increases. For the type of airgun array
planned for the proposed program, the
pathological (mortality) zone for
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crustaceans and cephalopods is
expected to be within a few meters of
the seismic source, at most; however,
very few specific data are available on
levels of seismic signals that might
damage these animals. This premise is
based on the peak pressure and rise/
decay time characteristics of seismic
airgun arrays currently in use around
the world.
Some studies have suggested that
seismic survey sound has a limited
pathological impact on early
developmental stages of crustaceans
(Pearson et al., 1994; Christian et al.,
2003; DFO, 2004). However, the impacts
appear to be either temporary or
insignificant compared to what occurs
under natural conditions. Controlled
field experiments on adult crustaceans
(Christian et al., 2003, 2004; DFO, 2004)
and adult cephalopods (McCauley et al.,
2000a,b) exposed to seismic survey
sound have not resulted in any
significant pathological impacts on the
animals. It has been suggested that
exposure to commercial seismic survey
activities has injured giant squid
(Guerra et al., 2004), but the article
provides little evidence to support this
claim.
Andre et al. (2011) exposed four
cephalopod species (Loligo vulgaris,
Sepia officinalis, Octopus vulgaris, and
Ilex coindetii) to two hours of
continuous sound from 50 to 400 Hz at
157 ± 5 dB re: 1 mPa. They reported
lesions to the sensory hair cells of the
statocysts of the exposed animals that
increased in severity with time,
suggesting that cephalopods are
particularly sensitive to low-frequency
sound.
The received SPL was reported as 157
± 5 dB re: 1 mPa, with peak levels at 175
dB re 1 mPa. As in the McCauley et al.
(2003) paper on sensory hair cell
damage in pink snapper as a result of
exposure to seismic sound, the
cephalopods were subjected to higher
sound levels than they would be under
natural conditions, and they were
unable to swim away from the sound
source.
Physiological Effects—Physiological
effects refer mainly to biochemical
responses by marine invertebrates to
acoustic stress. Such stress potentially
could affect invertebrate populations by
increasing mortality or reducing
reproductive success. Primary and
secondary stress responses (i.e., changes
in haemolymph levels of enzymes,
proteins, etc.) of crustaceans have been
noted several days or months after
exposure to seismic survey sounds
(Payne et al., 2007). The periods
necessary for these biochemical changes
to return to normal are variable and
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depend on numerous aspects of the
biology of the species and of the sound
stimulus.
Behavioral Effects—There is
increasing interest in assessing the
possible direct and indirect effects of
seismic and other sounds on
invertebrate behavior, particularly in
relation to the consequences for
fisheries. Changes in behavior could
potentially affect such aspects as
reproductive success, distribution,
susceptibility to predation, and
catchability by fisheries. Studies
investigating the possible behavioral
effects of exposure to seismic survey
sound on crustaceans and cephalopods
have been conducted on both uncaged
and caged animals. In some cases,
invertebrates exhibited startle responses
(e.g., squid in McCauley et al., 2000a,b).
In other cases, no behavioral impacts
were noted (e.g., crustaceans in
Christian et al., 2003, 2004; DFO, 2004).
There have been anecdotal reports of
reduced catch rates of shrimp shortly
after exposure to seismic surveys;
however, other studies have not
observed any significant changes in
shrimp catch rate (Andriguetto-Filho et
al., 2005). Similarly, Parry and Gason
(2006) did not find any evidence that
lobster catch rates were affected by
seismic surveys. Any adverse effects on
crustacean and cephalopod behavior or
fisheries attributable to seismic survey
sound depend on the species in
question and the nature of the fishery
(season, duration, fishing method).
Proposed 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 adverse impact on such
species or stock and its habitat, paying
particular attention to rookeries, mating
grounds, and areas of similar
significance, and the availability of such
species or stock for taking for certain
subsistence uses.
L–DEO has based the mitigation
measures described herein, to be
implemented for the proposed seismic
survey, on the following:
(1) Protocols used during previous L–
DEO seismic research cruises as
approved by NMFS;
(2) Previous IHA applications and
IHAs approved and authorized by
NMFS; and
(3) Recommended best practices in
Richardson et al. (1995), Pierson et al.
(1998), and Weir and Dolman, (2007).
To reduce the potential for
disturbance from acoustic stimuli
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associated with the activities, L–DEO
and/or its designees would implement
the following mitigation measures for
marine mammals:
(1) Proposed EZs;
(2) Power-down procedures;
(3) Shutdown procedures; and
(4) Ramp-up procedures.
Proposed Exclusion Zones—L–DEO
uses safety radii to designate EZs and to
estimate take for marine mammals.
Table 1 (presented earlier in this
document) shows the distances at which
three sound levels (160–, 180–, and
190–dB) are expected to be received
from the 36-airgun array and a single
airgun. The 180-dB and 190-dB level
shut-down criteria are applicable to
cetaceans and pinnipeds, respectively,
as specified by NMFS (2000); and L–
DEO used these levels to establish the
EZs.
If the protected species visual
observer (PSVO) detects marine
mammal(s) within or about to enter the
appropriate EZ, the Langseth crew will
immediately power down the airgun
array, or perform a shut down if
necessary (see Shut-down Procedures).
Power-down Procedures—A powerdown involves decreasing the number of
airguns in use such that the radius of
the 180-dB (or 190-dB) zone is
decreased to the extent that marine
mammals are no longer in or about to
enter the EZ. A power down of the
airgun array can also occur when the
vessel is moving from one seismic line
to another. During a power-down for
mitigation, L–DEO will operate one
airgun (40 in 3). The continued
operation of one airgun is intended to
alert marine mammals to the presence of
the seismic vessel in the area. In
contrast, a shutdown occurs when the
Langseth suspends all airgun activity.
If the PSVO detects a marine mammal
outside the EZ, which is likely to enter
the EZ, L–DEO will power-down the
airguns before the animal enters the EZ.
Likewise, if a mammal is already within
the EZ, when first detected L–DEO will
power-down the airguns immediately.
During a power down of the airgun
array, L–DEO will operate the 40-in 3
airgun. If a marine mammal is detected
within or near the smaller EZ around
that single airgun (Table 1), L–DEO will
shut down the airgun (see next section).
Following a power-down, L–DEO will
not resume airgun activity until the
marine mammal has cleared the safety
zone. L–DEO will consider the animal to
have cleared the EZ if:
• A PSVO has visually observed the
animal leave the EZ, or
• A PSVO has not sighted the animal
within the EZ for 15 min for species
with shorter dive durations (i.e., small
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odontocetes or pinnipeds), or 30 min for
species with longer dive durations (i.e.,
mysticetes and large odontocetes,
including sperm, pygmy sperm, dwarf
sperm, and beaked whales); or
• The vessel has moved outside the
EZ (e.g., if a marine mammal is sighted
close to the vessel and the ship speed
is 8.5 km km/h (5.3 mph), it would take
the vessel approximately eight minutes
to leave the vicinity of the marine
mammal).
During airgun operations following a
power-down or shutdown whose
duration has exceeded the time limits
specified previously, L–DEO will ramp
up the airgun array gradually (see
Shutdown and Ramp-up Procedures).
Shut-down Procedures—L–DEO will
shut down the operating airgun(s) if a
marine mammal is seen within or
approaching the EZ for the single
airgun. L–DEO will implement a shutdown:
(1) If an animal enters the EZ of the
single airgun after L–DEO has initiated
a power down; or
(2) If an animal is initially seen within
the EZ of the single airgun when more
than one airgun (typically the full
airgun array) is operating.
L–DEO will not resume airgun
activity until the marine mammal has
cleared the EZ, or until the PSVO is
confident that the animal has left the
vicinity of the vessel. Criteria for
judging that the animal has cleared the
EZ will be as described in the preceding
section.
Considering the conservation status
for north Pacific right whales, L–DEO
will shut down the airgun(s)
immediately in the unlikely event that
this species is observed, regardless of
the distance from the Langseth. L–DEO
will only begin a ramp-up if the right
whale has not been seen for 30 min.
Ramp-up Procedures—L–DEO will
follow a ramp-up procedure when the
airgun subarrays begin operating after a
specified period without airgun
operations or when a power down has
exceeded that period. L–DEO proposes
that, for the present cruise, this period
will be approximately eight minutes.
This period is based on the 180-dB
radius (940 m; 3,083 ft) for the 36-airgun
array towed at a depth of 9 m (29.5 ft)
in relation to the minimum planned
speed of the Langseth while shooting
(8.5 km/h; 5.3 mph; 4.6 kts). L–DEO has
used similar periods (8–10 min) during
previous L–DEO surveys. L–DEO will
not resume operations if a marine
mammal has not cleared the EZ as
described earlier.
Ramp-up will begin with the smallest
airgun in the array (40-in 3). Airguns
will be added in a sequence such that
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the source level of the array will
increase in steps not exceeding six dB
per five-minute period over a total
duration of approximately 30 min.
During ramp-up, the PSVOs will
monitor the EZ, and if he/she sights a
marine mammal, L–DEO will
implement a power down or shut down
as though the full airgun array were
operational.
If the complete EZ is not visible to the
PSVO for at least 30 min prior to the
start of operations in either daylight or
nighttime, L–DEO will not commence
the ramp-up unless at least one airgun
(40-in3 or similar) has been operating
during the interruption of seismic
survey operations. Given these
provisions, it is likely that L–DEO will
not ramp up the airgun array from a
complete shut-down at night or in thick
fog, because the outer part of the EZ for
that array will not be visible during
those conditions. If one airgun has
operated during a power-down period,
ramp-up to full power will be
permissible at night or in poor visibility,
on the assumption that marine
mammals will be alerted to the
approaching seismic vessel by the
sounds from the single airgun and could
move away. L–DEO will not initiate a
ramp-up of the airguns if a marine
mammal is sighted within or near the
applicable EZs during the day or close
to the vessel at night.
NMFS has carefully evaluated the
applicant’s proposed mitigation
measures and has considered a range of
other measures in the context of
ensuring that NMFS prescribed the
means of effecting the least practicable
adverse impact on the affected marine
mammal species and stocks and their
habitat. NMFS’ evaluation of potential
measures included consideration of the
following factors in relation to one
another:
(1) The manner in which, and the
degree to which, the successful
implementation of the measure is
expected to minimize adverse impacts
to marine mammals;
(2) The proven or likely efficacy of the
specific measure to minimize adverse
impacts as planned; and
(3) The practicability of the measure
for applicant implementation.
Based on NMFS’ evaluation of the
applicant’s proposed measures, as well
as other measures considered by NMFS
or recommended by the public, NMFS
has preliminarily determined that the
mitigation measures provide the means
of effecting the least practicable adverse
impacts on marine mammals species or
stocks and their habitat, paying
particular attention to rookeries, mating
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4781
grounds, and areas of similar
significance.
Proposed Monitoring and Reporting
In order to issue an ITA for an
activity, section 101(a)(5)(D) of the
MMPA states that NMFS must set forth
‘‘requirements pertaining to the
monitoring and reporting of such
taking.’’ The MMPA implementing
regulations at 50 CFR 216.104 (a)(13)
indicate that requests for IHAs must
include the suggested means of
accomplishing the necessary monitoring
and reporting that will result in
increased knowledge of the species and
of the level of taking or impacts on
populations of marine mammals that are
expected to be present in the action
area.
Proposed Monitoring
L–DEO proposes to sponsor marine
mammal monitoring during the present
project, in order to implement the
mitigation measures that require realtime monitoring, and to satisfy the
monitoring requirements of the IHA. L–
DEO’s proposed Monitoring Plan is
described below this section. L–DEO
understands that this monitoring plan
will be subject to review by NMFS, and
that refinements may be required. The
monitoring work described here has
been planned as a self-contained project
independent of any other related
monitoring projects that may be
occurring simultaneously in the same
regions. L–DEO is prepared to discuss
coordination of its monitoring program
with any related work that might be
done by other groups insofar as this is
practical and desirable.
Vessel-based Visual Monitoring
L–DEO will position PSVOs aboard
the seismic source vessel to watch for
marine mammals near the vessel during
daytime airgun operations and during
any start-ups at night. PSVOs will also
watch for marine mammals near the
seismic vessel for at least 30 min prior
to the start of airgun operations after an
extended shut down (i.e., greater than
approximately eight minutes for this
proposed cruise). When feasible, the
PSVOs will conduct observations during
daytime periods when the seismic
system is not operating for comparison
of sighting rates and behavior with and
without airgun operations and between
acquisition periods. Based on PSVO
observations, the Langseth will power
down or shut down the airguns when
marine mammals are observed within or
about to enter a designated EZ. The EZ
is a region in which a possibility exists
of adverse effects on animal hearing or
other physical effects.
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During seismic operations on the
Shatsky Rise, at least four protected
species observers (PSO) (i.e., either a
PSVO and/or a protected species
acoustic observer (PSAO)) will be based
aboard the Langseth. L–DEO will
appoint the PSOs with NMFS’
concurrence. The PSOs will conduct
observations during ongoing daytime
operations and nighttime ramp-ups of
the airgun array. During the majority of
seismic operations, two PSVOs will be
on duty from the observation tower to
monitor marine mammals near the
seismic vessel. Use of two simultaneous
PSVOs will increase the effectiveness of
detecting animals near the source
vessel. However, during mealtimes and
bathroom breaks, it is sometimes
difficult to have two PSVOs on effort,
but at least one PSVO will be on watch
during bathroom breaks and mealtimes.
PSVOs will be on duty in shifts of no
longer than four hours in duration.
Two PSVOs will also be on visual
watch during all nighttime ramp-ups of
the seismic airguns. A third PSAO will
monitor the PAM equipment 24 hours a
day to detect vocalizing marine
mammals present in the action area. In
summary, a typical daytime cruise
would have scheduled two PSVOs on
duty from the observation tower, and a
third PSAO on PAM. Other crew will
also be instructed to assist in detecting
marine mammals and implementing
mitigation requirements (if practical).
Before the start of the seismic survey,
the crew will be given additional
instruction on how to do so.
The Langseth is a suitable platform for
marine mammal observations. When
stationed on the observation platform,
the eye level will be approximately 21.5
m (70.5 ft) above sea level, and the
observer will have a good view around
the entire vessel. During daytime, the
PSVOs will scan the area around the
vessel systematically with reticle
binoculars (e.g., 7x50 Fujinon), Big-eye
binoculars (25x150), and with the naked
eye. During darkness, night vision
devices (NVDs) will be available (ITT
F500 Series Generation 3 binocularimage intensifier or equivalent), when
required. Laser range-finding binoculars
(Leica LRF 1200 laser rangefinder or
equivalent) will be available to assist
with distance estimation. Those are
useful in training observers to estimate
distances visually, but are generally not
useful in measuring distances to
animals directly; that is done primarily
with the reticles in the binoculars.
When the PSVOs observe marine
mammals within or about to enter the
designated EZ, the Langseth will
immediately power-down or shut-down
the airguns if necessary. The PSVO(s)
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will continue to maintain watch to
determine when the animal(s) are
outside the EZ by visual confirmation.
Airgun operations will not resume until
the animal is confirmed to have left the
EZ, or if not observed after 15 min for
species with shorter dive durations
(small odontocetes and pinnipeds) or 30
min for species with longer dive
durations (mysticetes and large
odontocetes, including sperm, pygmy
sperm, dwarf sperm, killer, and beaked
whales).
Passive Acoustic Monitoring
Passive Acoustic Monitoring (PAM)
will complement the visual monitoring
program, when practicable. Visual
monitoring typically is not effective
during periods of poor visibility or at
night, and even with good visibility, is
unable to detect marine mammals when
they are below the surface or beyond
visual range. Acoustical monitoring can
be used in conjunction with visual
observations to improve detection,
identification, and localization of
cetaceans. The acoustic monitoring will
serve to alert visual observers (if on
duty) when vocalizing cetaceans are
detected. It is only useful when marine
mammals call, but it can be effective
either by day or by night, and does not
depend on good visibility. The PSAO
will monitor the system in real time so
that he/she can advise the PSVO when
cetaceans are detected. When bearings
(primary and mirror-image) to calling
cetacean(s) are determined, the bearings
will be relayed to the visual observer to
help him/her sight the calling animal(s).
The PAM system consists of hardware
(i.e., hydrophones) and software. The
‘‘wet end’’ of the system consists of a
towed hydrophone array that is
connected to the vessel by a tow cable.
The tow cable is 250 m (820.2 ft) long,
and the hydrophones are fitted in the
last 10 m (32.8 ft) of cable. A depth
gauge is attached to the free end of the
cable, and the cable is typically towed
at depths less than 20 m (65.6 ft). L–
DEO will deploy the array from a winch
located on the back deck. A deck cable
will connect the tow cable to the
electronics unit in the main computer
lab where the acoustic station, signal
conditioning, and processing system
will be located. The acoustic signals
received by the hydrophones are
amplified, digitized, and then processed
by the Pamguard software. The system
can detect marine mammal
vocalizations at frequencies up to 250
kHz.
One PSAO, an expert bioacoustician
with primary responsibility for PAM
will be aboard the Langseth in addition
to the four PSVOs. The PSAO will
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monitor the towed hydrophones 24 h
per day during airgun operations and
during most periods when the Langseth
is underway while the airguns are not
operating. However, PAM may not be
possible if damage occurs to both the
primary and back-up hydrophone arrays
during operations. The primary PAM
streamer on the Langseth is a digital
hydrophone streamer. Should the digital
streamer fail, back-up systems should
include an analog spare streamer and a
hull-mounted hydrophone.
One PSAO will monitor the acoustic
detection system by listening to the
signals from two channels via
headphones and/or speakers and
watching the real-time spectrographic
display for frequency ranges produced
by cetaceans. The PSAO monitoring the
acoustical data will be on shift for one
to six hours at a time. The other PSVOs
are expected to rotate through the PAM
position, although the expert PSAO will
be on PAM duty more frequently.
When a vocalization is detected while
visual observations are in progress, the
PSAO on duty will contact the visual
PSVO immediately, to alert him/her to
the presence of cetaceans (if they have
not already been seen), and to allow a
power down or shut down to be
initiated, if required. The information
regarding the call will be entered into a
database. Data entry will include an
acoustic encounter identification
number, whether it was linked with a
visual sighting, date, time when first
and last heard and whenever any
additional information was recorded,
position and water depth when first
detected, bearing if determinable,
species or species group (e.g.,
unidentified dolphin, sperm whale),
types and nature of sounds heard (e.g.,
clicks, continuous, sporadic, whistles,
creaks, burst pulses, strength of signal,
etc.), and any other notable information.
The acoustic detection can also be
recorded for further analysis.
PSVO Data and Documentation
PSVOs will record data to estimate
the numbers of marine mammals
exposed to various received sound
levels and to document apparent
disturbance reactions or lack thereof.
Data will be used to estimate numbers
of animals potentially ‘taken’ by
harassment (as defined in the MMPA).
They will also provide information
needed to order a power down or shut
down of the airguns when a marine
mammal is within or near the EZ.
When a sighting is made, the
following information about the sighting
will be recorded:
1. Species, group size, age/size/sex
categories (if determinable), behavior
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when first sighted and after initial
sighting, heading (if consistent), bearing
and distance from seismic vessel,
sighting cue, apparent reaction to the
airguns or vessel (e.g., none, avoidance,
approach, paralleling, etc.), and
behavioral pace.
2. Time, location, heading, speed,
activity of the vessel, sea state,
visibility, and sun glare.
The data listed under (2) will also be
recorded at the start and end of each
observation watch, and during a watch
whenever there is a change in one or
more of the variables.
All observations and power downs or
shut downs will be recorded in a
standardized format. Data will be
entered into an electronic database. The
accuracy of the data entry will be
verified by computerized data validity
checks as the data are entered and by
subsequent manual checking of the
database. These procedures will allow
initial summaries of data to be prepared
during and shortly after the field
program, and will facilitate transfer of
the data to statistical, graphical, and
other programs for further processing
and archiving.
Results from the vessel-based
observations will provide:
1. The basis for real-time mitigation
(airgun power down or shut down).
2. Information needed to estimate the
number of marine mammals potentially
taken by harassment, which must be
reported to NMFS.
3. Data on the occurrence,
distribution, and activities of marine
mammals and turtles in the area where
the seismic study is conducted.
4. Information to compare the
distance and distribution of marine
mammals and turtles relative to the
source vessel at times with and without
seismic activity.
5. Data on the behavior and
movement patterns of marine mammals
seen at times with and without seismic
activity.
Proposed Reporting
L–DEO will submit a report to NMFS
and NSF within 90 days after the end of
the cruise. The report will describe the
operations that were conducted and
sightings of marine mammals and
turtles near the operations. The report
will provide full documentation of
methods, results, and interpretation
pertaining to all monitoring. The 90-day
report will summarize the dates and
locations of seismic operations, and all
marine mammal sightings (dates, times,
locations, activities, associated seismic
survey activities). The report will also
include estimates of the number and
nature of exposures that could result in
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‘‘takes’’ of marine mammals by
harassment or in other ways.
In the unanticipated event that the
specified activity clearly causes the take
of a marine mammal in a manner
prohibited by the IHA (if issued), such
as an injury (Level A harassment),
serious injury or mortality (e.g., shipstrike, gear interaction, and/or
entanglement), L–DEO 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, at 301–
427–8401 and/or by email to
Michael.Payne@noaa.gov and
ITP.Cody@noaa.gov and the NMFS
Pacific Islands Regional Stranding
Coordinator at 808–944–2269
(David.Schofield@noaa.gov). 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 L–DEO to
determine what is necessary to
minimize the likelihood of further
prohibited take and ensure MMPA
compliance. L–DEO may not resume
their activities until notified by NMFS
via letter, email, or telephone.
In the event that L–DEO discovers an
injured or dead marine mammal, and
the lead PSVO 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), L–
DEO will immediately report the
incident to the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, at 301–
427–8401 and/or by email to
Michael.Payne@noaa.gov and
ITP.Cody@noaa.gov and the NMFS
Pacific Islands Regional Stranding
Coordinator at 808–944–2269
(David.Schofield@noaa.gov). The report
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4783
must include the same information
identified in the paragraph above this
section. Activities may continue while
NMFS reviews the circumstances of the
incident. NMFS will work with L–DEO
to determine whether modifications in
the activities are appropriate.
In the event that L–DEO discovers an
injured or dead marine mammal, and
the lead PSVO determines that the
injury or death is not associated with or
related to the activities authorized in the
IHA (e.g., previously wounded animal,
carcass with moderate to advanced
decomposition, or scavenger damage),
L–DEO will report the incident to the
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS, at 301–427–8401 and/or by
email to Michael.Payne@noaa.gov and
ITP.Cody@noaa.gov and the NMFS
Pacific Islands Regional Stranding
Coordinator at 808–944–2269
(David.Schofield@noaa.gov), within 24
hours of the discovery. L–DEO will
provide photographs or video footage (if
available) or other documentation of the
stranded animal sighting to NMFS.
Estimated Take by Incidental
Harassment
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].
Only take by Level B harassment is
proposed to be authorized as a result of
the marine geophysical survey in the
northwestern Pacific Ocean. Acoustic
stimuli (i.e., increased underwater
sound) generated during the operation
of the seismic airgun array may have the
potential to cause marine mammals in
the survey area to be exposed to sounds
at or greater than 160 dB or cause
temporary, short-term changes in
behavior. There is no evidence that the
planned activities could result in injury,
serious injury or mortality within the
specified geographic area for which L–
DEO seeks the IHA. The required
mitigation and monitoring measures
will minimize any potential risk for
injury, serious injury, or mortality.
The following sections describe L–
DEO’s methods to estimate take by
incidental harassment and present the
applicant’s estimates of the numbers of
marine mammals that could be affected
during the proposed seismic program.
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The estimates are based on a
consideration of the number of marine
mammals that could be disturbed
appreciably by operations with the 36airgun array to be used during
approximately 1,216 km (755.6 mi) of
survey lines on the Shatsky Rise in the
northwestern Pacific Ocean.
L–DEO assumes that, during
simultaneous operations of the airgun
array and the other sources, any marine
mammals close enough to be affected by
the MBES and SBP would already be
affected by the airguns. However,
whether or not the airguns are operating
simultaneously with the other sources,
marine mammals are expected to exhibit
no more than short-term and
inconsequential responses to the MBES
and SBP given their characteristics (e.g.,
narrow downward-directed beam) and
other considerations described
previously. Such reactions are not
considered to constitute ‘‘taking’’
(NMFS, 2001). Therefore, L–DEO
provides no additional allowance for
animals that could be affected by sound
sources other than airguns.
Density data on 18 marine mammal
species in the Shatsky Rise area are
available from two sources using
conventional line transect methods:
Japanese sighting surveys conducted
since the early 1980s, and fisheries
observers in the high-seas driftnet
fisheries during 1987–1990 (see Table 3
in L–DEO’s application).
For the 16 other marine mammal
species that could be encountered in the
proposed survey area, data from the
western North Pacific right whale are
not available (see Table 3 in L–DEO’s
application). L–DEO is not aware of any
density estimates for three of those
species—Hubb’s (Mesoplodon
carlhubbsi), Stejneger’s (Mesoplodon
stejnegeri), and gingko-toothed beaked
whales (Mesoplodon ginkgodens). For
the remaining 13 species out of the 16,
(see Table 3 in L–DEO’s application),
density estimates are available from
other areas of the Pacific: 11 species
from the offshore stratum of the 2002
Hawaiian Islands survey (Barlow, 2006)
and two species from surveys of the
California Current ecosystem off the
U.S. west coast between 1991 and 2005
(Barlow and Forney, 2007). Those
estimates are based on standard linetransect protocols developed by NMFS’
Southwest Fisheries Science Center
(SWFSC).
Densities for 14 species are available
from Japanese sighting surveys in the
Shatsky Rise survey area. Miyashita
(1993a) provided estimates for six
dolphin species in this area that have
been taken in the Japanese drive
fisheries. The densities used here are
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Miyashita’s (1993a) estimates for the
‘Eastern offshore’ survey area (30–42° N,
145°–180° E). Kato and Miyashita (1998)
provided estimates for sperm whale
densities from Japanese sightings data
during 1982 to 1996 in the western
North Pacific (20–50° N, 130°–180° E),
and Hakamada et al. (2004) provided
density estimates for sei whales during
August through September in the
JARPN II sub-areas 8 and 9 (35–50° N,
150–170° E excluding waters in the
Exclusive Economic Zone of Russia)
during 2002 and 2003. L–DEO used
density estimates during 1994 through
2007 for minke whales at 35–40° N,
157–170° E from Hakamada et al.
(2009), density estimates during 1998
through 2002 for Bryde’s whales at 31–
43° N, 145–165° E from Kitakado et al.
(2008), and density estimates during
1994–2007 for blue, fin, humpback, and
North Pacific right whales at 31–51° N,
140–170° E from Matsuoka et al. (2009).
For four species (northern fur seal,
Dall’s porpoise, Pacific white-sided
dolphin (Lagenorhynchus obliquidens),
northern right-whale dolphin
(Lissodelphis borealis)), estimates of
densities in the Shatsky Rise area are
available from sightings data collected
by observers in the high-seas driftnet
fisheries during 1987 through 1990
(Buckland et al., 1993). Those data were
analyzed for 5° × 5° blocks, and the
densities used here are from blocks for
which available data overlap the
proposed survey area. In general, those
data represent the average annual
density in the northern half of the
Shatsky Rise survey area (35–40° N).
The densities mentioned above had
been corrected by the original authors
for detectability bias and, with the
exception of Kitakado et al. (2008) and
Hakamada et al. (2009), for availability
bias. Detectability bias is associated
with diminishing sightability with
increasing lateral distance from the
track line [f(0)]. Availability bias refers
to the fact that there is less than a 100
percent probability of sighting an
animal that is present along the survey
track line, and it is measured by g(0).
There is some uncertainty about the
accuracy of the density data from the
Japanese Whale Research Program
under Special Permit (JARPN/JARPN II).
For example, The available densities in
Miyashita (1993a) and Buckland et al.
(1993) are from the 1980s; although
these densities represent the best
available information for the Shatsky
Rise area at present, they will be biased
if abundance or distributions of those
species have changed since the data
were collected. Therefore, there is
uncertainty with respect to the expected
marine mammal densities during this
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time. However, the approach used here
is based on the best available data.
The estimated numbers of individuals
potentially exposed are based on the
160-dB re: 1 mPa criterion for all
cetaceans (see Table 3 in this notice). It
is assumed that marine mammals
exposed to airgun sounds that strong
might change their behavior sufficiently
to be considered ‘‘taken by harassment.’’
L–DEO’s estimates of exposures to
various sound levels assume that the
proposed surveys will be completed; in
fact, the ensonified areas calculated
using the planned number of linekilometers have been increased by 25
percent to accommodate turns, lines
that may need to be repeated,
equipment testing, etc. As is typical
during ship surveys, inclement weather
and equipment malfunctions are likely
to cause delays and may limit the
number of useful line-kilometers of
seismic operations that can be
undertaken. Furthermore, any marine
mammal sightings within or near the
designated exclusion zone will result in
the shutdown of seismic operations as a
mitigation measure. Thus, the following
estimates of the numbers of marine
mammals potentially exposed to 160-dB
re 1 mPa sounds are precautionary, and
probably overestimate the actual
numbers of marine mammals that might
be involved. These estimates assume
that there will be no weather,
equipment, or mitigation delays, which
is highly unlikely.
L–DEO estimated the number of
different individuals that may be
exposed to airgun sounds with received
levels greater than or equal to 160 dB re:
1 mPa on one or more occasions by
considering the total marine area that
would be within the 160-dB radius
around the operating airgun array on at
least one occasion and the expected
density of marine mammals. The
number of possible exposures
(including repeated exposures of the
same individuals) can be estimated by
considering the total marine area that
would be within the 160-dB radius
around the operating airguns, including
areas of overlap. In the proposed survey,
the majority of seismic lines are widely
spaced in the survey area, so few
individual mammals would be exposed
numerous times during the survey. The
area including overlap is only 1.01
times the area excluding overlap, so a
marine mammal that stayed in the
survey area during the entire survey
could be exposed only once. However,
it is unlikely that a particular animal
would stay in the area during the entire
survey.
The number of different individuals
potentially exposed to received levels
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greater than or equal to 160 re: 1 mPa
was calculated by multiplying:
(1) The expected species density,
times;
(2) The anticipated area to be
ensonified to that level during airgun
operations excluding overlap, which is
approximately 10,971 square kilometers
(km2) (4,235.9 square miles (mi2)).
The area expected to be ensonified
was determined by entering the planned
survey lines into a MapInfo GIS, using
the GIS to identify the relevant areas by
‘‘drawing’’ the applicable 160-dB buffer
(see Table 1 in this document) around
each seismic line, and then calculating
the total area within the buffers. Areas
of overlap were included only once
when estimating the number of
individuals exposed. Applying this
approach, approximately 9,229 km2
(3,563 mi2) (11,536 km2; 4,454 mi2
including the 25 percent contingency)
would be within the 160-dB isopleth on
one or more occasions during the
survey. Because this approach does not
allow for turnover in the mammal
populations in the study area during the
course of the survey, the actual number
of individuals exposed could be
underestimated. However, the approach
assumes that no cetaceans will move
away from or toward the trackline as the
Langseth approaches in response to
increasing sound levels prior to the time
the levels reach 160 dB, which will
result in overestimates for those species
known to avoid seismic vessels.
The total estimate of the number of
individual cetaceans that could be
exposed to seismic sounds with
received levels greater than or equal to
160 dB re: 1 mPa during the survey is
7,354 (see Table 3). That total includes
74 baleen whales, 39 of which are
endangered: 5 humpback whales or
0.53% of the regional population, 21 sei
whales (0.21%), 9 fin whales (0.05%),
and 4 blue whales (0.13%). In addition,
12 sperm whales (also listed as
endangered under the ESA) or 0.04% of
the regional population could be
exposed during the survey, and 108
beaked whales including Cuvier’s,
Longman’s, Baird’s, and Blainville’s
beaked whales. Most (96 percent) of the
cetaceans potentially exposed are
delphinids; short-beaked common,
striped, pantropical spotted, and Pacific
white-sided dolphins are estimated to
be the most common species in the area,
with estimates of 3,569 (0.12% of the
regional population), 1,374 (0.24%), 812
(0.19%), and 420 (0.04%) exposed to
greater than or equal to 160 dB re: 1 mPa,
respectively.
TABLE 3—ESTIMATES OF THE POSSIBLE NUMBERS OF MARINE MAMMALS EXPOSED TO DIFFERENT SOUND LEVELS
DURING L–DEO’S SEISMIC SURVEY IN THE NORTHWESTERN PACIFIC OCEAN DURING MARCH THROUGH APRIL, 2012
Estimated
number of individuals exposed
to sound levels ≥
160 dB re: 1
μPa1
Species
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North Pacific right whale ..................................................................................................
Humpback whale .............................................................................................................
Minke whale .....................................................................................................................
Bryde’s whale ..................................................................................................................
Sei whale .........................................................................................................................
Fin whale .........................................................................................................................
Blue whale .......................................................................................................................
Sperm whale ....................................................................................................................
Pygmy sperm whale ........................................................................................................
Dwarf sperm whale ..........................................................................................................
Cuvier’s beaked whale ....................................................................................................
Baird’s beaked whale ......................................................................................................
Longman’s beaked whale ................................................................................................
Blainville’s beaked whale .................................................................................................
Rough-toothed dolphin ....................................................................................................
Bottlenose dolphin ...........................................................................................................
Pantropical spotted dolphin .............................................................................................
Spinner dolphin ................................................................................................................
Striped dolphin .................................................................................................................
Fraser’s dolphin ...............................................................................................................
Short-beaked common dolphin ........................................................................................
Pacific white-sided dolphin ..............................................................................................
Northern right whale dolphin ...........................................................................................
Risso’s dolphin .................................................................................................................
Melon-headed whale .......................................................................................................
False killer whale .............................................................................................................
Killer whale ......................................................................................................................
Short-finned pilot whale ...................................................................................................
Dall’s porpoise .................................................................................................................
Northern fur seal ..............................................................................................................
Requested or
adjusted take
authorization
0
5
29
6
21
9
4
12
37
90
78
10
5
15
36
277
812
10
1374
53
3569
420
5
125
15
24
2
58
253
21
22
5
29
6
21
9
4
12
37
90
78
10
3 18
15
36
277
812
2 32
1374
2 286
3569
420
5
125
2 89
24
73
2 65
253
21
Approximate
percent of
regional
population 3
0.23
0.53
0.12
0.03
0.21
0.05
0.13
0.04
N.A.
<0.01
0.39
N.A.
N.A.
0.06
0.02
0.16
0.19
<0.01
0.24
0.02
0.12
0.04
<0.01
0.01
0.03
0.15
0.02
0.11
0.02
<0.01
1 Estimates
are based on densities in Table 3 and an ensonified area (including 25% contingency 11,536 km2).
Take Authorization increased to mean group size from density sources in Table 3 of L–DEO’s application.
3 Regional population size estimates are from Table 3 of L–DEO’s application; NA means not available.
2 Requested
Encouraging and Coordinating
Research
L–DEO and NSF will coordinate the
planned marine mammal monitoring
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program associated with the seismic
survey in the northwestern Pacific
Ocean with other parties that may have
interest in the area and/or be conducting
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marine mammal studies in the same
region during the seismic survey.
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Negligible Impact and Small Numbers
Analysis and Determination
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.’’ In making a
negligible impact determination, NMFS
considers:
(1) The number of anticipated
injuries, serious injuries, or mortalities;
(2) The number, nature, and intensity,
and duration of Level B harassment (all
relatively limited); and
(3) The context in which the takes
occur (i.e., impacts to areas of
significance, impacts to local
populations, and cumulative impacts
when taking into account successive/
contemporaneous actions when added
to baseline data);
(4) The status of stock or species of
marine mammals (i.e., depleted, not
depleted, decreasing, increasing, stable,
impact relative to the size of the
population);
(5) Impacts on habitat affecting rates
of recruitment/survival; and
(6) The effectiveness of monitoring
and mitigation measures.
For reasons stated previously in this
document, the specified activities
associated with the marine seismic
survey are not likely to cause PTS, or
other non-auditory injury, serious
injury, or death because:
(1) The likelihood that, given
sufficient notice through relatively slow
ship speed, marine mammals are
expected to move away from a noise
source that is annoying prior to its
becoming potentially injurious;
(2) The potential for temporary or
permanent hearing impairment is
relatively low and would likely be
avoided through the incorporation of
the required monitoring and mitigation
measures (described previously in this
document);
(3) The fact that cetaceans would have
to be closer than 940 m (3,084 ft) in
deep water when the 36-airgun array is
in use at 9 m (29.5 ft) tow depth, and
40 m (131.2 ft) in deep water when the
single airgun is in use at 9 m from the
vessel to be exposed to levels of sound
believed to have even a minimal chance
of causing PTS; and
(4) The likelihood that marine
mammal detection ability by trained
PSVOs is high at close proximity to the
vessel.
No injuries, serious injuries, or
mortalities are anticipated to occur as a
result of the L–DEO’s planned marine
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Jkt 226001
seismic survey, and none are proposed
to be authorized by NMFS. Only shortterm behavioral disturbance is
anticipated to occur due to the brief and
sporadic duration of the survey
activities. Table 3 of this document
outlines the number of requested Level
B harassment takes that are anticipated
as a result of these activities. Due to the
nature, degree, and context of Level B
(behavioral) harassment anticipated and
described (see ‘‘Potential Effects on
Marine Mammals’’ section in this
notice), the activity is not expected to
impact rates of recruitment or survival
for any affected species or stock.
Additionally, the seismic survey will
not adversely impact marine mammal
habitat.
Many animals perform vital functions,
such as feeding, resting, traveling, and
socializing, on a diel cycle (i.e., 24 hr
cycle). Behavioral reactions to noise
exposure (such as disruption of critical
life functions, displacement, or
avoidance of important habitat) are
more likely to be significant if they last
more than one diel cycle or recur on
subsequent days (Southall et al., 2007).
While seismic operations are
anticipated to occur on consecutive
days, the entire duration of the survey
is not expected to last more than
approximately 23 days (i.e., 7 days of
seismic operations, 16 days of transit)
and the Langseth will be continuously
moving along planned tracklines that
are geographically spread-out.
Therefore, the seismic survey will be
increasing sound levels in the marine
environment in a relatively small area
surrounding the vessel, which is
constantly travelling over far distances,
for a relatively short time period (i.e.,
one week) in the study area.
Of the 34 marine mammal species
under NMFS’ jurisdiction that are
known to occur or likely to occur in the
study area, six of these species are listed
as endangered under the ESA: the blue,
fin, humpback, north Pacific right, sei,
and sperm whales. These species are
also categorized as depleted under the
MMPA. L–DEO has requested
authorized take for the six listed
species. To protect these animals (and
other marine mammals in the study
area), L–DEO must cease or reduce
airgun operations if animals enter
designated zones. No injury, serious
injury, or mortality is expected to occur
and due to the nature, degree, and
context of the Level B harassment
anticipated. The activity is not expected
to impact rates of recruitment or
survival.
As mentioned previously, NMFS
estimates that 30 species of marine
mammals under its jurisdiction could be
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potentially affected by Level B
harassment over the course of the IHA.
For each species, these numbers are
small (each, less than one percent)
relative to the regional population size.
NMFS provided the population
estimates for the marine mammal
species that may be taken by Level B
harassment in Table 2 of this document.
NMFS’ practice has been to apply the
160 dB re: 1 mPa received level
threshold for underwater impulse sound
levels to determine whether take by
Level B harassment occurs. Southall et
al. (2007) provides a severity scale for
ranking observed behavioral responses
of both free-ranging marine mammals
and laboratory subjects to various types
of anthropogenic sound (see Table 4 in
Southall et al. [2007]).
NMFS has preliminarily determined,
provided that the aforementioned
mitigation and monitoring measures are
implemented, that the impact of
conducting a marine seismic survey on
the Shatsky Rise in the northwestern
Pacific Ocean, March to April, 2012,
may result, at worst, in a temporary
modification in behavior and/or lowlevel physiological effects (Level B
harassment) of small numbers of certain
species of marine mammals. See Table
3 for the requested authorized take
numbers of cetaceans.
While behavioral modifications,
including temporarily vacating the area
during the operation of the airgun(s),
may be made by these species to avoid
the resultant acoustic disturbance, the
availability of alternate areas within
these areas and the short and sporadic
duration of the research activities, have
led NMFS to preliminary determine that
this action will have a negligible impact
on the species in the specified
geographic region.
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
mitigation and monitoring measures,
NMFS preliminarily finds that L–DEO’s
planned research activities will result in
the incidental take of small numbers of
marine mammals, by Level B
harassment only, and that the total
taking from the marine seismic survey
will have a negligible impact on the
affected species or stocks of marine
mammals; and that impacts to affected
species or stocks of marine mammals
have been mitigated to the lowest level
practicable.
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Impact on Availability of Affected
Species or Stock for Taking for
Subsistence Uses
Section 101(a)(5)(D) of the MMPA
also requires NMFS to determine that
the authorization will not have an
unmitigable adverse effect on the
availability of marine mammal species
or stocks for subsistence use. There are
no relevant subsistence uses of marine
mammals in the study area (Shatsky
Rise, northwestern Pacific Ocean) that
implicate MMPA section 101(a)(5)(D).
Endangered Species Act
Of the species of marine mammals
that may occur in the proposed survey
area, several are listed as endangered
under the ESA, including the blue, fin,
humpback, north Pacific right, sei, and
sperm whales. L–DEO did not request
take of endangered western north
Pacific gray whales because of the low
likelihood of encountering these species
during the cruise.
Under section 7 of the ESA, NSF has
initiated formal consultation with the
NMFS’, Office of Protected Resources,
Endangered Species Act Interagency
Cooperation Division, on this proposed
seismic survey. NMFS’ Office of
Protected Resources, Permits and
Conservation Division, had initiated
formal consultation under section 7 of
the ESA with NMFS’ Office of Protected
Resources, Endangered Species Act
Interagency Cooperation Division, to
obtain a Biological Opinion (BiOp)
evaluating the effects of issuing an IHA
for threatened and endangered marine
mammals and, if appropriate,
authorizing incidental take. NMFS will
conclude formal section 7 consultation
prior to making a determination on
whether or not to issue the IHA. If the
IHA is issued, NSF and L–DEO, in
addition to the mitigation and
monitoring requirements included in
the IHA, will be required to comply
with the Terms and Conditions of the
Incidental Take Statement
corresponding to NMFS’ BiOp issued to
both NSF and NMFS’ Office of Protected
Resources.
wreier-aviles on DSK5TPTVN1PROD with NOTICES
National Environmental Policy Act
(NEPA)
To meet NMFS’ National
Environmental Policy Act (NEPA; 42
U.S.C. 4321 et seq.) requirements for the
issuance of an IHA to L–DEO, NMFS
will prepare an Environmental
Assessment (EA) titled ‘‘Issuance of an
Incidental Harassment Authorization to
the Lamont-Doherty Earth Observatory
to Take Marine Mammals by
Harassment Incidental to a Marine
Geophysical Survey in the Northwest
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15:20 Jan 30, 2012
Jkt 226001
Pacific Ocean, March through April,
2012.’’ This EA will incorporate the
NSF’s Environmental Analysis Pursuant
To Executive Order 12114 (NSF, 2010)
and an associated report (Report)
prepared by LGL Limited
Environmental Research Associates
(LGL) for NSF, titled, ‘‘Environmental
Assessment of a Marine Geophysical
Survey by the R/V Marcus G. Langseth
in the Northwest Pacific Ocean,
March—April, 2012,’’ by reference
pursuant to 40 CFR 1502.21 and NOAA
Administrative Order (NAO) 216–6
§ 5.09(d). Prior to making a final
decision on the IHA application, NMFS
will make a decision of whether or not
to issue a Finding of No Significant
Impact (FONSI).
Proposed Authorization
As a result of these preliminary
determinations, NMFS proposes to
authorize the take of marine mammals
incidental to L–DEO’s proposed marine
seismic survey in the northwest Pacific
Ocean, provided the previously
mentioned mitigation, monitoring, and
reporting requirements are incorporated.
The duration of the IHA would not
exceed one year from the date of its
issuance.
Information Solicited
NMFS requests interested persons to
submit comments and information
concerning this proposed project and
NMFS’s preliminary determination of
issuing an IHA (see ADDRESSES).
Concurrent with the publication of this
notice in the Federal Register, NMFS is
forwarding copies of this application to
the Marine Mammal Commission and
its Committee of Scientific Advisors.
Dated: January 25, 2012.
Helen M. Golde,
Deputy Director, Office of Protected
Resources, National Marine Fisheries Service.
[FR Doc. 2012–2076 Filed 1–30–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF DEFENSE
Office of the Secretary
Department of Defense Task Force on
the Care, Management, and Transition
of Recovering Wounded, Ill, and
Injured Members of the Armed Forces;
Amended Meeting Notice
Department of Defense, Office
of the Assistant Secretary of Defense.
ACTION: Amended meeting notice.
AGENCY:
Under the provisions of the
Federal Advisory Committee Act of
1972 (5 U.S.C., Appendix, as amended),
SUMMARY:
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4787
the Government in the Sunshine Act of
1976 (5 U.S.C. 552b, as amended), and
41 CFR 102–3.150, the Department of
Defense announces a change to the
previously announced meeting of the
Department of Defense Task Force on
the Care, Management, and Transition
of Recovering Wounded, Ill, and Injured
Members of the Armed Forces. The
meeting notice published in the January
24, 2012 edition of the Federal Register
(77 FR 3454) is amended to reflect
changes in the meeting times and
agenda. All other text in the previously
announced meeting remains the same.
DATES: Tuesday, February 21, 2012–
Thursday, February 23, 2012, from 8
a.m. to 5:30 p.m. EST, each day.
FOR FURTHER INFORMATION CONTACT: Mail
Delivery service through Recovering
Warrior Task Force, Hoffman Building
II, 200 Stovall St., Alexandria, VA
22332–0021 ‘‘Mark as Time Sensitive
for February Meeting.’’ Emails to
rwtf@wso.whs.mil. Denise F. Dailey,
Designated Federal Officer; Telephone
(703) 325–6640. Fax (703) 325–6710.
SUPPLEMENTARY INFORMATION:
Purpose of the Meeting: The purpose
of the meeting is for the Task Force
Members to convene and gather data
from panels and briefers on the Task
Force’s topics of inquiry.
Agenda: (Please refer to https://
dtf.defense.gov/rwtf/meetings.html for
the most up-to-date meeting
information).
Day 1: Tuesday, February 21
8–9:30 a.m. Site Visit Review &
Administration
9:30–9:45 a.m. Break
9:45–10:45 a.m. Continue Site Visit
Review and Administration
10:45–11:45 a.m. WWCTP
11:45 a.m.–12:45 p.m. Lunch
12:45–2:15 p.m. Army WTC Briefing
2:15–2:30 p.m. Break
2:30–4 p.m. Air Force Programs for
Wounded, Ill, and Injured Briefing
4–5 p.m. FRCP Update
5–5:30 p.m. Close
Day 2: Wednesday, February 22
8–8:30 a.m. Public Forum
8:30–9:30 a.m. TRICARE Management
Activity Telephone Survey of Ill or
Injured Service Members PostOperational Deployment, Dr. Richard
R. Bannick
9:30–9:45 a.m. Break
9:45–10:45 a.m. OSD Office of Military
Community and Family Policy
(MCFP)
10:45–11:45 a.m. SOCOM Care
Coalition Update
11:45 a.m.–12:45 p.m. Lunch
12:45–2:15 p.m. Navy Safe Harbor
Update
E:\FR\FM\31JAN1.SGM
31JAN1
Agencies
[Federal Register Volume 77, Number 20 (Tuesday, January 31, 2012)]
[Notices]
[Pages 4765-4787]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2076]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XA879
Takes of Marine Mammals Incidental to Specified Activities;
Marine Geophysical Survey in the Northwest Pacific Ocean, March Through
April 2012
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental harassment authorization; request
for comments.
-----------------------------------------------------------------------
[[Page 4766]]
SUMMARY: NMFS has received an application from Lamont-Doherty Earth
Observatory (L-DEO), a part of Columbia University, for an Incidental
Harassment Authorization (IHA) to take marine mammals, by harassment,
incidental to conducting a marine geophysical survey in the northwest
Pacific Ocean, March through April, 2012.
DATES: Comments and information must be received no later than March 1,
2012.
ADDRESSES: Comments on the application should be addressed to P.
Michael Payne, Chief, Permits and Conservation Division, Office of
Protected Resources, National Marine Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910-3225. The mailbox address for
providing email comments is ITP.Cody@noaa.gov. NMFS is not responsible
for email comments sent to addresses other than the one provided here.
Comments sent via email, including all attachments, must not exceed a
10-megabyte file size.
All comments received are a part of the public record and will
generally be posted to https://www.nmfs.noaa.gov/pr/permits/incidental.htm#applications without change. All Personal Identifying
Information (for example, name, address, etc.) voluntarily submitted by
the commenter may be publicly accessible. Do not submit confidential
business information or otherwise sensitive or protected information.
An electronic copy of the application containing a list of the
references used in this document may be obtained by writing to the
above address, telephoning the contact listed here (see FOR FURTHER
INFORMATION CONTACT) or visiting the internet at: https://www.nmfs.noaa.gov/pr/permits/incidental.htm#applications.
The following associated documents are also available at the same
internet address: the National Science Foundation's (NSF) draft
Environmental Analysis (EA) pursuant to Executive Order 12114. The EA
incorporates an ``Environmental Assessment of a Marine Geophysical
Survey by the R/V Marcus G. Langseth in the Northwest Pacific Ocean,
March-April, 2012,'' prepared by LGL Limited, on behalf of NSF.
Documents cited in this notice may be viewed, by appointment, during
regular business hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT: Jeannine Cody, Office of Protected
Resources, NMFS, (301) 427-8401.
SUPPLEMENTARY INFORMATION:
Background
Section 101(a)(5)(D) of the Marine Mammal Protection Act of 1972,
as amended (MMPA; 16 U.S.C. 1361 et seq.) directs the Secretary of
Commerce to authorize, upon request, the incidental, but not
intentional, taking of small numbers of marine mammals of a species or
population stock, by United States citizens who engage in a specified
activity (other than commercial fishing) within a specified
geographical region if certain findings are made and, if the taking is
limited to harassment, a notice of a proposed authorization is provided
to the public for review.
Authorization for the incidental taking of small numbers of marine
mammals shall be granted if NMFS finds that the taking will have a
negligible impact on the species or stock(s), and will not have an
unmitigable adverse impact on the availability of the species or
stock(s) for subsistence uses (where relevant). The authorization must
set forth the permissible methods of taking, other means of effecting
the least practicable adverse impact on the species or stock and its
habitat, and requirements pertaining to the mitigation, monitoring and
reporting of such takings. 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.''
Section 101(a)(5)(D) of the MMPA established an expedited process
by which citizens of the United States can apply for an authorization
to incidentally take small numbers of marine mammals by harassment.
Section 101(a)(5)(D) of the MMPA establishes a 45-day time limit for
NMFS' review of an application followed by a 30-day public notice and
comment period on any proposed authorizations for the incidental
harassment of small numbers of marine mammals. Within 45 days of the
close of the public comment period, NMFS must either issue or deny the
authorization. NMFS must publish a notice in the Federal Register
within 30 days of its determination to issue or deny the authorization.
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
NMFS received an application on October 31, 2011, from L-DEO for
the taking by harassment, of marine mammals, incidental to conducting a
marine geophysical survey in the northwest Pacific Ocean in
international waters. Upon receipt of additional information, NMFS
determined the application complete and adequate on December 23, 2011.
L-DEO, with research funding from the U.S. National Science
Foundation (NSF), plans to conduct the survey from March 24, 2012,
through April 16, 2012. L-DEO received an IHA in 2010 to conduct the
same specified activity in the same location. However, due to medical
emergencies, L-DEO suspended its operations and was unable to complete
the seismic survey. Thus, this 2011 survey will allow L-DEO to acquire
data necessary to complete the abbreviated 2010 study.
L-DEO plans to use one source vessel, the R/V Marcus G. Langseth
(Langseth), a seismic airgun array and a single hydrophone streamer to
conduct a geophysical survey at the Shatsky Rise, a large igneous
plateau in the northwest Pacific Ocean. The proposed survey will
provide data necessary to decipher the crustal structure of the Shatsky
Rise; may address major questions of earth history, geodynamics, and
tectonics; could impact the understanding of terrestrial magmatism and
mantle convection; and may obtain data that could be used to improve
estimates of regional earthquake occurrence and distribution. In
addition to the operations of the seismic airgun array and hydrophone
streamer, L-DEO intends to operate a multibeam echosounder (MBES) and a
sub-bottom profiler (SBP) continuously throughout the survey.
Acoustic stimuli (i.e., increased underwater sound) generated
during the operation of the seismic airgun array, may have the
potential to cause a short-term behavioral disturbance for marine
mammals in the survey area. This is the principal means of marine
mammal taking associated with these activities and L-DEO has requested
an authorization to take 30 species of marine mammals by Level B
harassment. Take is not expected to result from the use of the MBES or
the SBP for reasons discussed in this notice. Also, NMFS does not
expect take to result from collision with the Langseth because it is a
single vessel moving at
[[Page 4767]]
relatively slow speeds (4.6 knots (kts); 8.5 km per hr (km/h); 5.3
miles (mi) per hour (mph)) during seismic acquisition within the
survey, for a relatively short period of time. It is likely that any
marine mammal would be able to avoid the vessel.
Description of the Specified Activity
L-DEO's proposed seismic survey on the Shatsky Rise is scheduled to
commence on March 24, 2012 and end on April 16, 2012. The Langseth
would depart from Yokohama, Japan on March 24, 2012 and transit to the
survey area in the northwest Pacific Ocean, approximately 1,200
kilometers (km) (745.6 miles (mi)) in international waters offshore of
the east coast of Japan. At the conclusion of the survey activities,
the Langseth proposes to arrive in Honolulu, Hawaii, on April 16, 2012.
Some minor deviation from these dates is possible, depending on
logistics, weather conditions, and the need to repeat some lines if
data quality is substandard. Therefore, NMFS proposes to issue an
authorization that is effective from March 24, 2012 to May 7, 2012.
Geophysical survey activities will involve 3-D seismic
methodologies to decipher the crustal structure of the Shatsky Rise. To
obtain high-resolution, 2-D structures of the area's magmatic systems
and thermal structures, the Langseth will deploy a 36-airgun array as
an energy source and a 6-km-long (3.7 mi-long) hydrophone streamer. As
the airgun array is towed along the survey lines, the hydrophone
streamer will receive the returning acoustic signals and transfer the
data to the vessel's on-board processing system.
The proposed study (e.g., equipment testing, startup, line changes,
repeat coverage of any areas, and equipment recovery) will require
approximately 7 days (d) to complete approximately 1,216 km (755.6 mi)
of transect lines. The Langseth will conduct additional seismic
operations in the survey area associated with turns, airgun testing,
and repeat coverage of any areas where the initial data quality is sub-
standard. Data acquisition will include approximately 168 hours (hr) of
airgun operations (7 d x 24 hr).
L-DEO, the Langseth's operator, will conduct all planned seismic
data acquisition activities, with on-board assistance by the scientists
who have proposed the study. The Principal Investigators for this
survey are Drs. Jun Korenaga (Yale University, New Haven, CT) and
William Sager (Texas A&M University, College Station, TX). The vessel
will be self-contained, and the crew will live aboard the vessel for
the entire cruise.
Description of the Specified Geographic Region
L-DEO will conduct the proposed survey in international waters in
the northwest Pacific Ocean. The study area will encompass an area on
the Shatsky Rise bounded by approximately 33.5-36 degrees ([deg]) North
by 156-161[deg] East (see Figure 1 in L-DEO's application). Water
depths in the survey area range from approximately 3,000 to 5,000
meters (m) (1.9 to 3.1 mi).
Vessel Specifications
The Langseth, owned by NSF, is a seismic research vessel with a
propulsion system designed to be as quiet as possible to avoid
interference with the seismic signals emanating from the airgun array.
The vessel, which has a length of 71.5 m (235 feet (ft)); a beam of
17.0 m (56 ft); a maximum draft of 5.9 m (19 ft); and a gross tonnage
of 3,834 pounds, is powered by two 3,550 horsepower (hp) Bergen BRG-6
diesel engines which drive two propellers. Each propeller has four
blades and the shaft typically rotates at 750 revolutions per minute.
The vessel also has an 800-hp bowthruster, which is not used during
seismic acquisition. The Langseth's operation speed during seismic
acquisition will be approximately 4.6 kts (8.5 km/h; 5.3 mph) and the
cruising speed of the vessel outside of seismic operations is 18.5 km/h
(11.5 mph or 10 kts).
The Langseth will tow the 36-airgun array, as well as the
hydrophone streamer, along predetermined lines. When the Langseth is
towing the airgun array and the hydrophone streamer, the turning rate
of the vessel is limited to five degrees per minute. Thus, the
maneuverability of the vessel is limited during operations with the
streamer.
The vessel also has an observation tower from which protected
species visual observers (PSVO) will watch for marine mammals before
and during the proposed airgun operations. When stationed on the
observation platform, the PSVO's eye level will be approximately 21.5 m
(71 ft) above sea level providing the PSVO an unobstructed view around
the entire vessel.
Acoustic Source Specifications
Seismic Airguns
The Langseth will deploy a 36-airgun array, with a total volume of
approximately 6,600 cubic inches (in\3\) at a tow depth of 9 m (29.5
ft). The airguns are a mixture of Bolt 1500LL and Bolt 1900LLX airguns
ranging in size from 40 to 360 in\3\, with a firing pressure of 1,900
pounds per square inch. The dominant frequency components range from
zero to 188 Hertz (Hz). The array configuration consists of four
identical linear strings, with 10 airguns on each string; the first and
last airguns will be spaced 16 m (52 ft) apart. Of the 10 airguns, nine
will fire simultaneously while the tenth airgun will serve as a spare
and will be turned on in case of failure of one of the other airguns.
The Langseth will distribute the array across an area of approximately
24 x 16 m (78.7 x 52.5 ft) and will tow the array approximately 140 m
(459.3 ft) behind the vessel. The tow depth of the array will be 9 m
(29.5 ft).
During the multichannel seismic (MCS) survey, each airgun array
will emit a pulse at approximately 20-second (s) intervals which
corresponds to a shot interval of approximately 50 m (164 ft). During
firing, the airguns will emit a brief (approximately 0.1 s) pulse of
sound; during the intervening periods of operations, the airguns will
be silent.
Metrics Used in This Document
This section includes a brief explanation of the sound measurements
frequently used in the discussions of acoustic effects in this
document. Sound pressure is the sound force per unit area, and is
usually measured in micropascals ([mu]Pa), where 1 pascal (Pa) is the
pressure resulting from a force of one newton exerted over an area of
one square meter. Sound pressure level (SPL) is expressed as the ratio
of a measured sound pressure and a reference level. The commonly used
reference pressure level in underwater acoustics is 1 [mu]Pa, and the
units for SPLs are dB re: 1 [mu]Pa.
SPL (in decibels (dB)) = 20 log (pressure/reference pressure)
SPL is an instantaneous measurement and can be expressed as the
peak, the peak-peak (p-p), or the root mean square (rms). Root mean
square, which is the square root of the arithmetic average of the
squared instantaneous pressure values, is typically used in discussions
of the effects of sounds on vertebrates and all references to SPL in
this document refer to the root mean square unless otherwise noted. SPL
does not take the duration of a sound into account.
Characteristics of the Airgun Pulses
Airguns function by venting high-pressure air into the water which
creates an air bubble. The pressure signature of an individual airgun
consists of a sharp rise and then fall in pressure, followed
[[Page 4768]]
by several positive and negative pressure excursions caused by the
oscillation of the resulting air bubble. The oscillation of the air
bubble transmits sounds downward through the seafloor and the amount of
sound transmitted in the near horizontal directions is reduced.
However, the airgun array also emits sounds that travel horizontally
toward non-target areas.
The nominal source levels of the airgun array used by L-DEO on the
Langseth is 236 to 265 dB re: 1 [mu]Pa(p-p) and the rms
value for a given airgun pulse is typically 16 dB re: 1 [mu]Pa lower
than the peak-to-peak value (Greene, 1997; McCauley et al., 1998,
2000a). However, the difference between rms and peak or peak-to-peak
values for a given pulse depends on the frequency content and duration
of the pulse, among other factors.
Accordingly, L-DEO has predicted the received sound levels in
relation to distance and direction from the 36-airgun array and the
single Bolt 1900LL 40-in\3\ airgun, which will be used during power
downs. A detailed description of L-DEO's modeling for marine seismic
source arrays for species mitigation is provided in Appendix A of NSF's
EA. These are the nominal source levels applicable to downward
propagation. The effective source levels for horizontal propagation are
lower than those for downward propagation because of the directional
nature of the sound from the airgun array. Appendix B(3) of NSF's EA
discusses the characteristics of the airgun pulses. NMFS refers the
reviewers to the IHA application and EA documents for additional
information.
Predicted Sound Levels for the Airguns
Tolstoy et al., (2009) reported results for propagation
measurements of pulses from the Langseth's 36-airgun, 6,600 in\3\ array
in shallow-water (approximately 50 m (164 ft)) and deep-water depths
(approximately 1,600 m (5,249 ft)) in the Gulf of Mexico in 2007 and
2008. Results of the Gulf of Mexico calibration study (Tolstoy et al.,
2009) showed that radii around the airguns for various received levels
varied with water depth and that sound propagation varied with array
tow depth.
L-DEO used the results from the Gulf of Mexico study to determine
the algorithm for its model that calculates the exclusion zones (EZ)
for the 36-airgun array and the single airgun. L-DEO uses these values
to designate mitigation zones and to estimate take (described in
greater detail in Section VII of L-DEO's application and Section IV of
NSF's EA) for marine mammals.
Comparison of the Tolstoy et al. calibration study with L-DEO's
model for the Langseth's 36-airgun array indicated that the model
represents the actual received levels, within the first few kilometers,
where the predicted EZs are located. However, the model for deep water
(greater than 1,000 m; 3,280 ft) overestimated the received sound
levels at a given distance but is still valid for defining exclusion
zones at various tow depths. Because the tow depth of the array in the
calibration study is less shallow (6 m; 19.7 ft) than the tow depth
array in the proposed survey (9 m; 29.5 ft), L-DEO used correction
factors for estimating the received levels in deep water during the
proposed survey. The correction factors used were the ratios of the
160-,180-, and 190-dB distances from the modeled results for the 6,600
in\3\ airgun array towed at 6 m (19.7 ft) versus 9 m (29.5 ft) from LGL
(2008); 1.285, 1.338, and 1.364 respectively. For a single airgun, the
tow depth has minimal effect on the maximum near-field output and the
shape of the frequency spectrum for the single airgun; thus, the
predicted EZs are essentially the same at different tow depths. The L-
DEO model does not allow for bottom interactions, and thus is most
directly applicable to deep water.
Table 1 summarizes the predicted distances at which sound levels
(160- and 180-dB) are expected to be received from the 36-airgun array
and a single airgun operating in deep water. To avoid the potential for
injury, NMFS (1995, 2000) concluded that cetaceans should not be
exposed to pulsed underwater noise at received levels exceeding 180 dB
re: 1 [mu]Pa. NMFS believes that to avoid the potential for permanent
physiological damage (Level A harassment), cetaceans should not be
exposed to pulsed underwater noise at received levels exceeding 180 dB
re: 1 [mu]Pa. The 180-dB level is a shutdown criterion applicable to
cetaceans, as specified by NMFS (2000); these levels were used to
establish the EZs. NMFS also assumes that cetaceans exposed to levels
exceeding 160 dB re: 1 [mu]Pa (rms) may experience Level B harassment.
Table 1--Measured (Array) or Predicted (Single Airgun) Distances To Which Sound Levels Greater Than or Equal to
160 and 180 dB re: 1 [mu]PaRms That Could Be Received in Deep Water Using a 36-Airgun Array, as Well as a Single
Airgun Towed at a Depth of 9 m (29.5 ft) During the Proposed Survey in the Northwest Pacific Ocean, During March-
April, 2012
[Distances Are Based On Model Results Provided By L-DEO]
----------------------------------------------------------------------------------------------------------------
Predicted RMS Distances (m)
Source and volume Water depth -----------------------------------------------------
160 dB 180 dB 190 dB
----------------------------------------------------------------------------------------------------------------
Single Bolt airgun (40 in\3\)...... Deep (>1,000 m)...... 385 40 12
36-Airgun Array.................... ..................... 3,850 940 400
----------------------------------------------------------------------------------------------------------------
Appendix A of NSF's EA discusses L-DEO's calculations for the
model. NMFS refers the reviewers to L-DEO's application and the NSF's
EA for additional information.
Multibeam Echosounder
The Langseth will operate a Kongsberg EM 122 MBES concurrently
during airgun operations to map characteristics of the ocean floor. The
hull-mounted MBES emits brief pulses of sound (also called a ping)
(10.5 to 13 kilohertz (kHz)) in a fan-shaped beam that extends downward
and to the sides of the ship. The transmitting beamwidth is one or two
degrees ([deg]) fore-aft and 150 [deg] athwartship and the maximum
source level is 242 dB re: 1 [mu]Pa.
For deep-water operations, each ping consists of eight (in water
greater than 1,000 m; 3,280 ft) or four (less than 1,000 m; 3,280 ft)
successive, fan-shaped transmissions, from two to 15 milliseconds (ms)
in duration and each ensonifying a sector that extends 1 [deg] fore-
aft. Continuous wave pulses increase from two to 15 milliseconds (ms)
long in water depths up to 2,600 m (8,530 ft). The MBES uses frequency-
modulated chirp pulses up to 100-ms long in water greater than 2,600 m
(8,530 ft). The eight successive transmissions span an overall cross-
track angular extent of about 150 [deg], with
[[Page 4769]]
2-ms gaps between the pulses for successive sectors.
Sub-bottom Profiler
The Langseth will also operate a Knudsen Chirp 3260 SBP
concurrently during airgun and MBES operations to provide information
about the sedimentary features and bottom topography. The SBP is
capable of reaching depths of 10,000 m (6.2 mi). The dominant frequency
component of the SBP is 3.5 kHz which is directed downward in a 27[deg]
cone by a hull-mounted transducer on the vessel. The nominal power
output is 10 kilowatts (kW), but the actual maximum radiated power is
three kW or 222 dB re: 1 [mu]Pa. The ping duration is up to 64 ms with
a pulse interval of one second, but a common mode of operation is to
broadcast five pulses at 1-s intervals followed by a 5-s pause.
NMFS expects that acoustic stimuli resulting from the proposed
operation of the single airgun or the 36-airgun array has the potential
to harass marine mammals, incidental to the conduct of the proposed
seismic survey. NMFS expects these disturbances to be temporary and
result in a temporary modification in behavior and/or low-level
physiological effects (Level B harassment only) of small numbers of
certain species of marine mammals. NMFS does not expect that the
movement of the Langseth, during the conduct of the seismic survey, has
the potential to harass marine mammals because of the relatively slow
operation speed of the vessel (4.6 kts; 8.5 km/hr; 5.3 mph) during
seismic acquisition.
Description of the Marine Mammals in the Area of the Specified Activity
Thirty-four marine mammal species may occur in the Shatsky Rise
survey area, including 26 odontocetes (toothed cetaceans), seven
mysticetes (baleen whales) and one species of pinniped during March
through April. Six of these species are listed as endangered under the
Endangered Species Act of 1973 (ESA; 16 U.S.C. 1531 et seq.), including
the blue (Balaenoptera musculus), fin (Balaenoptera physalus), humpback
(Megaptera novaeangliae), north Pacific right (Eubalaena japonica), sei
(Balaenoptera borealis), and sperm (Physeter macrocephalus) whales.
Based on available data, the western north Pacific gray whale
(Eschrichtius robustus) may have the potential to migrate off of the
Pacific coast of Japan (Reilly et al., 2008a), though any occurrence in
the survey area would be rare as gray whales are known to prefer
nearshore coastal waters. Based on available data, L-DEO does not
expect to encounter the western north Pacific gray whale within the
proposed study area and does not present analysis for these species.
Accordingly, NMFS did not consider this cetacean species in greater
detail and the proposed IHA will only address requested take
authorizations for the seven mysticetes, 26 odontocetes, and one
species of pinniped. The species of marine mammals expected to be most
common in the survey area (all delphinids) include the short-beaked
common (Delphinus delphis), striped (Stenella coeruleoalba), and
Fraser's (Lagenodelphis hosei) dolphins, and Dall's porpoise
(Phocoenoides dalli).
Table 2 presents information on the abundance, distribution, and
conservation status of the marine mammals that may occur in the
proposed survey area March through April, 2012.
Table 2--Habitat, Abundance, and Conservation Status of Marine Mammals That May Occur in or Near the Proposed
Seismic Survey Area on the Shatsky Rise in the Northwest Pacific Ocean
[See text and Tables 2 and 3 in L-DEO's application and the NSF's EA for further details]
----------------------------------------------------------------------------------------------------------------
Species Habitat Abundance in the NW Pacific ESA \1\ Density \2\
----------------------------------------------------------------------------------------------------------------
Mysticetes
North Pacific right whale. Pelagic, coastal. few 100 \3\................. EN............. 0.04
Humpback whale............ Mainly nearshore, 938-1107 \4\................ EN............. 0.47
banks.
Minke whale............... Pelagic, coastal. 25,000 \5\.................. NL............. 2.51
Bryde's whale............. Pelagic, coastal. 20,501 \6\.................. NL............. 0.52
Sei whale................. Primarily 7260-12,620 \7\............. EN............. 1.78
offshore,
pelagic.
Fin whale................. Continental 13,620-18,680 \8\........... EN............. 0.74
slope, mostly
pelagic.
Blue whale................ Pelagic, coastal. 3500 \9\.................... EN............. 0.39
Odontocetes
Sperm whale............... Usually pelagic, 29,674 \10\................. EN............. 1.04
deep sea.
Pygmy sperm whale......... Deep waters off N.A......................... NL............. 3.19
the shelf.
Dwarf sperm whale......... Deep waters off 11,200 \11\................. NL............. 7.82
the shelf.
Cuvier's beaked whale..... Pelagic.......... 20,000 \11\................. NL............. 6.80
Baird's beaked whale...... Deep water....... N.A......................... NL............. 0.88
Longman's beaked whale.... Deep water....... N.A......................... NL............. 0.45
Hubb's beaked whale....... Deep water....... 25,300 \12\................. NL............. 1.28
Ginkgo-toothed beaked Pelagic.......... 25,300 \12\................. NL............. 0.01
whale.
Blainville's beaked whale. Pelagic.......... 25,300 \12\................. NL............. 3.12
Stejneger's beaked whale.. Deep water....... 25,300 \12\................. NL............. 23.99
Rough-toothed dolphin..... Deep water....... 145,900 \11\................ NL............. 70.41
Common bottlenose dolphin. Coastal, oceanic, 168,000 \13\................ NL............. 0.83
shelf break.
Pantropical spotted Pelagic, coastal. 438,000 \13\................ NL............. 119.07
dolphin.
Spinner dolphin........... Pelagic, coastal. 801,000 \14\................ NL............. 4.57
Striped dolphin........... Off continental 570,000 \13\................ NL............. 309.35
shelf.
Fraser's dolphin.......... Waters >1000 m... 289,300 \11\................ NL............. 36.40
Short-beaked common Shelf, pelagic, 2,963,000 \15\.............. NL............. 0.41
dolphin. seamounts.
Pacific white-sided Continental 988,000 \16\................ NL............. 10.8
dolphin. slope, pelagic.
Northern right whale Deep water....... 307,000 \16\................ NL............. 1.32
dolphin.
Risso's dolphin........... Deep water, 838,000 \13\................ NL............. 0
seamounts.
Melon-headed whale........ Oceanic.......... 45,400 \11\................. NL............. 2.05
Pygmy killer whale........ Deep, pantropical 38,900 \11\................. NL............. 0.16
waters.
False killer whale........ Pelagic.......... 16,000 \13\................. NL............. 5.00
Killer whale.............. Widely 8500 \11\................... NL............. 21.94
distributed.
[[Page 4770]]
Short-finned pilot whale.. Mostly pelagic, 53,000 \13\................. NL............. 1.04
high-relief.
Dall's porpoise........... Deep water....... 1,337,224 \17\.............. NL............. 3.19
Pinnipeds
Northern fur seal......... Pelagic, coastal. 1.1 million \18\............ NL............. 1.79
----------------------------------------------------------------------------------------------------------------
N.A.--Not available or not assessed.
\1\ Endangered Species Act: EN = Endangered, NL = Not listed
\2\ Density estimate as listed in Table 3 of L-DEO's application. Refer to page 41 for specific references.
\3\ North Pacific (Jefferson et al. 2008).
\4\ Western North Pacific (Calambokidis et al. 2008).
\5\ Northwest Pacific and Okhotsk Sea (Buckland et al. 1992; IWC 2010a).
\6\ Western North Pacific (Kitakado et al. 2008; IWC 2010a).
\7\ North Pacific (Tillman 1977).
\8\ North Pacific (Ohsumi and Wada 1974).
\9\ North Pacific (NMFS 1998).
\10\ Western North Pacific (Whitehead 2002b).
\11\ Eastern Tropical Pacific (ETP) (Wade and Gerrodette 1993).
\12\ ETP; all Mesoplodon spp. (Wade and Gerrodette 1993).
\13\ Western North Pacific (Miyashita 1993a).
\14\ Whitebelly spinner dolphin in the ETP in 2000 (Gerrodette et al. 2005 in Hammond et al 2008a).
\15\ ETP (Gerrodette and Forcada 2002 in Hammond et al 2008b).
\16\ North Pacific (Miyashita 1993b).
\17\ North Pacific (Buckland et al 1993).
\18\ North Pacific, 2004-2005 (Gelatt and Lowry 2008).
NMFS refers the reader to Sections III and IV of L-DEO's
application for detailed information regarding the abundance and
distribution, population status, and life history and behavior of these
species and their occurrence in the proposed project area. The
application also presents how L-DEO calculated the estimated densities
for the marine mammals in the proposed survey area. NMFS has reviewed
these data and determined them to be the best available scientific
information for the purposes of the proposed IHA.
Potential Effects on Marine Mammals
Acoustic stimuli generated by the operation of the airguns, which
introduce sound into the marine environment, may have the potential to
cause Level B harassment of marine mammals in the proposed survey area.
The effects of sounds from airgun operations might include one or more
of the following: tolerance, masking of natural sounds, behavioral
disturbance, temporary or permanent impairment, or non-auditory
physical or physiological effects (Richardson et al., 1995; Gordon et
al., 2004; Nowacek et al., 2007; Southall et al., 2007).
Permanent hearing impairment, in the unlikely event that it
occurred, would constitute injury, but temporary threshold shift (TTS)
is not an injury (Southall et al., 2007). Although the possibility
cannot be entirely excluded, it is unlikely that the proposed project
would result in any cases of temporary or permanent hearing impairment,
or any significant non-auditory physical or physiological effects.
Based on the available data and studies described here, some behavioral
disturbance is expected, but NMFS expects the disturbance to be
localized and short-term.
Tolerance
Studies on marine mammals' tolerance to sound in the natural
environment are relatively rare. Richardson et al. (1995) defines
tolerance as the occurrence of marine mammals in areas where they are
exposed to human activities or manmade noise. In many cases, tolerance
develops by the animal habituating to the stimulus (i.e., the gradual
waning of responses to a repeated or ongoing stimulus) (Richardson, et
al., 1995; Thorpe, 1963), but because of ecological or physiological
requirements, many marine animals may need to remain in areas where
they are exposed to chronic stimuli (Richardson, et al., 1995).
Numerous studies have shown that pulsed sounds from airguns are
often readily detectable in the water at distances of many kilometers.
Several studies have shown that marine mammals at distances more than a
few kilometers from operating seismic vessels often show no apparent
response (see Appendix B(5) in NSF's EA). 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 the
marine mammal group. Although various baleen whales and toothed whales,
and (less frequently) pinnipeds have been shown to react behaviorally
to airgun pulses under some conditions, at other times marine mammals
of all three types have shown no overt reactions (Stone 2003; Stone and
Tasker 2006; Moulton et al. 2005, 2006a; Weir 2008a for sperm whales),
(MacLean and Koski 2005; Bain and Williams 2006 for Dall's porpoises).
The relative responsiveness of baleen and toothed whales are quite
variable.
Masking of Natural Sounds
The term masking refers to the inability of a subject to recognize
the occurrence of an acoustic stimulus as a result of the interference
of another acoustic stimulus (Clark et al., 2009). Introduced
underwater sound may, through masking, reduce the effective
communication distance of a marine mammal species if the frequency of
the source is close to that used as a signal by the marine mammal, and
if the anthropogenic sound is present for a significant fraction of the
time (Richardson et al., 1995).
NMFS expects the masking effects of pulsed sounds (even from large
arrays of airguns) on marine mammal calls and other natural sounds to
be limited, although there are very few specific data on this. Because
of the intermittent nature and low duty cycle of seismic
[[Page 4771]]
airgun pulses, animals can emit and receive sounds in the relatively
quiet intervals between pulses. However, in some situations,
reverberation occurs for much or the entire interval between pulses
(e.g., Simard et al., 2005; Clark and Gagnon, 2006) which could mask
calls. Some baleen and toothed whales are known to continue calling in
the presence of seismic pulses, and their calls can usually be heard
between the seismic pulses (e.g., Richardson et al., 1986; McDonald et
al., 1995; Greene et al., 1999; Nieukirk et al., 2004; Smultea et al.,
2004; Holst et al., 2005a,b, 2006; and Dunn and Hernandez, 2009).
However, Clark and Gagnon (2006) reported that fin whales in the
northeast Pacific Ocean went silent for an extended period starting
soon after the onset of a seismic survey in the area. Similarly, there
has been one report that sperm whales ceased calling when exposed to
pulses from a very distant seismic ship (Bowles et al., 1994). However,
more recent studies found that they continued calling in the presence
of seismic pulses (Madsen et al., 2002; Tyack et al., 2003; Smultea et
al., 2004; Holst et al., 2006; and Jochens et al., 2008). Dolphins and
porpoises commonly are heard calling while airguns are operating (e.g.,
Gordon et al., 2004; Smultea et al., 2004; Holst et al., 2005a, b; and
Potter et al., 2007). The sounds important to small odontocetes are
predominantly at much higher frequencies than are the dominant
components of airgun sounds, thus limiting the potential for masking.
In general, NMFS expects the masking effects of seismic pulses to
be minor, given the normally intermittent nature of seismic pulses.
Refer to Appendix B(4) of NSF's EA for a more detailed discussion of
masking effects on marine mammals.
Behavioral Disturbance
Disturbance includes a variety of effects, including subtle to
conspicuous changes in behavior, movement, and displacement. Reactions
to sound, if any, depend on species, state of maturity, experience,
current activity, reproductive state, time of day, and many other
factors (Richardson et al., 1995; Wartzok et al., 2004; Southall et
al., 2007; Weilgart, 2007). If a marine mammal does react briefly to an
underwater sound by changing its behavior or moving a small distance,
the impacts of the change are unlikely to be significant to the
individual, let alone the stock or population. However, if a sound
source displaces marine mammals from an important feeding or breeding
area for a prolonged period, impacts on individuals and populations
could be significant (e.g., Lusseau and Bejder, 2007; Weilgart, 2007).
Given the many uncertainties in predicting the quantity and types of
impacts of noise on marine mammals, it is common practice to estimate
how many mammals would be present within a particular distance of
industrial activities and/or exposed to a particular level of
industrial sound. In most cases, this approach likely overestimates the
numbers of marine mammals that would be affected in some biologically-
important manner.
The sound criteria used to estimate how many marine mammals might
be disturbed to some biologically-important degree by a seismic program
are based primarily on behavioral observations of a few species.
Scientists have conducted detailed studies on humpback, gray, bowhead
(Balaena mysticetus), and sperm whales. Less detailed data are
available for some other species of baleen whales, small toothed
whales, and sea otters (Enhydra lutris), but for many species there are
no data on responses to marine seismic surveys.
Baleen Whales--Baleen whales generally tend to avoid operating
airguns, but avoidance radii are quite variable (reviewed in Richardson
et al., 1995). Whales are often reported to show no overt reactions to
pulses from large arrays of airguns at distances beyond a few
kilometers, even though the airgun pulses remain well above ambient
noise levels out to much longer distances. However, as reviewed in
Appendix B(5) of the NSF's EA, baleen whales exposed to strong noise
pulses from airguns often react by deviating from their normal
migration route and/or interrupting their feeding and moving away from
the area. In the cases of migrating gray and bowhead whales, the
observed changes in behavior appeared to be of little or no biological
consequence to the animals (Richardson et al., 1995). They simply
avoided the sound source by displacing their migration route to varying
degrees, but within the natural boundaries of the migration corridors.
Studies of gray, bowhead, and humpback whales have shown that
seismic pulses with received levels of 160 to 170 dB re: 1 [mu]Pa seem
to cause obvious avoidance behavior in a substantial fraction of the
animals exposed (Malme et al., 1986, 1988; Richardson et al., 1995). In
many areas, seismic pulses from large arrays of airguns diminish to
those levels at distances ranging from four to 15 km from the source. A
substantial proportion of the baleen whales within those distances may
show avoidance or other strong behavioral reactions to the airgun
array. Subtle behavioral changes sometimes become evident at somewhat
lower received levels, and studies summarized in Appendix B(5) of NSF's
EA have shown that some species of baleen whales, notably bowhead and
humpback whales, at times show strong avoidance at received levels
lower than 160-170 dB re: 1 [mu]Pa.
Researchers have studied the responses of humpback whales to
seismic surveys during migration, feeding during the summer months,
breeding while offshore from Angola, and wintering offshore from
Brazil. McCauley et al. (1998, 2000a) studied the responses of humpback
whales off western Australia to a full-scale seismic survey with a 16-
airgun array (2,678-in\3\) and to a single, 20-in\3\ airgun with source
level of 227 dB re: 1 [micro]Pa (p-p). In the 1998 study, the
researchers documented that avoidance reactions began at five to eight
km (3.1 to 4.9 mi) from the array, and that those reactions kept most
pods approximately three to four km (1.9 to 2.5 mi) from the operating
seismic boat. In the 2000 study, McCauley et al. noted localized
displacement during migration of four to five km (2.5 to 3.1 mi) by
traveling pods and seven to 12 km (4.3 to 7.5 mi) by more sensitive
resting pods of cow-calf pairs. Avoidance distances with respect to the
single airgun were smaller but consistent with the results from the
full array in terms of the received sound levels. The mean received
level for initial avoidance of an approaching airgun was 140 dB re: 1
[mu]Pa for humpback pods containing females, and at the mean closest
point of approach distance, the received level was 143 dB re: 1 [mu]Pa.
The initial avoidance response generally occurred at distances of five
to eight km (3.1 to 4.9 mi) from the airgun array and two km (1.2 mi)
from the single airgun. However, some individual humpback whales,
especially males, approached within distances of 100 to 400 m (328 to
1,312 ft), where the maximum received level was 179 dB re: 1 [mu]Pa.
Data collected by observers during several seismic surveys in the
northwest Atlantic Ocean showed that sighting rates of humpback whales
were significantly greater during non-seismic periods compared with
periods when a full array was operating (Moulton and Holst, 2010). In
addition, humpback whales were more likely to swim away and less likely
to swim towards a vessel during seismic versus non-seismic periods
(Moulton and Holst, 2010).
Humpback whales on their summer feeding grounds in Frederick Sound
and Stephens Passage, Alaska did not
[[Page 4772]]
exhibit persistent avoidance when exposed to seismic pulses from a
1.64-L (100-in\3\) airgun (Malme et al., 1985). Some humpbacks seemed
``startled'' at received levels of 150 to 169 dB re: 1 [mu]Pa. Malme et
al. (1985) concluded that there was no clear evidence of avoidance,
despite the possibility of subtle effects, at received levels up to 172
re: 1 [mu]Pa.
Other studies have suggested that south Atlantic humpback whales
wintering off Brazil may be displaced or even strand upon exposure to
seismic surveys (Engel et al., 2004). Although, the evidence for this
was circumstantial and subject to alternative explanations (IAGC,
2004). Also, the evidence was not consistent with subsequent results
from the same area of Brazil (Parente et al., 2006), or with direct
studies of humpbacks exposed to seismic surveys in other areas and
seasons. After allowance for data from subsequent years, there was ``no
observable direct correlation'' between strandings and seismic surveys
(IWC, 2007: 236).
There are no data on reactions of right whales to seismic surveys,
but results from the closely-related bowhead whale show that their
responsiveness can be quite variable depending on their activity
(migrating versus feeding). Bowhead whales migrating west across the
Alaskan Beaufort Sea in autumn, in particular, are unusually
responsive, with substantial avoidance occurring out to distances of 20
to 30 km (12.4 to 18.6 mi) from a medium-sized airgun source at
received sound levels of approximately 120 to 130 dB re: 1 [mu]Pa
(Miller et al., 1999; Richardson et al., 1999; see Appendix B(5) of
NSF's EA). However, more recent research on bowhead whales (Miller et
al., 2005; Harris et al., 2007) corroborates earlier evidence that,
during the summer feeding season, bowheads are not as sensitive to
seismic sources. Nonetheless, subtle but statistically significant
changes in surfacing--respiration--dive cycles were evident upon
statistical analysis (Richardson et al., 1986). In the summer, bowheads
typically begin to show avoidance reactions at received levels of about
152 to 178 dB re: 1 [mu]Pa (Richardson et al., 1986, 1995; Ljungblad et
al., 1988; Miller et al., 2005).
Reactions of migrating and feeding (but not wintering) gray whales
to seismic surveys have been studied. Malme et al. (1986, 1988) studied
the responses of feeding eastern Pacific gray whales to pulses from a
single 100-in\3\ airgun off St. Lawrence Island in the northern Bering
Sea. They estimated, based on small sample sizes, that 50 percent of
feeding gray whales stopped feeding at an average received pressure
level of 173 dB re: 1 [mu]Pa on an (approximate) rms basis, and that 10
percent of feeding whales interrupted feeding at received levels of 163
dB re: 1 [micro]Pa. Those findings were generally consistent with the
results of experiments conducted on larger numbers of gray whales that
were migrating along the California coast (Malme et al., 1984; Malme
and Miles, 1985), and western Pacific gray whales feeding off Sakhalin
Island, Russia (Wursig et al., 1999; Gailey et al., 2007; Johnson et
al., 2007; Yazvenko et al., 2007a,b), along with data on gray whales
off British Columbia (Bain and Williams, 2006).
Various species of Balaenoptera (blue, sei, fin, and minke whales)
have occasionally been seen in areas ensonified by airgun pulses
(Stone, 2003; MacLean and Haley, 2004; Stone and Tasker, 2006), and
calls from blue and fin whales have been localized in areas with airgun
operations (e.g., McDonald et al., 1995; Dunn and Hernandez, 2009;
Castellote et al., 2010). Sightings by observers on seismic vessels off
the United Kingdom from 1997 to 2000 suggest that, during times of good
sightability, sighting rates for mysticetes (mainly fin and sei whales)
were similar when large arrays of airguns were shooting vs. silent
(Stone, 2003; Stone and Tasker, 2006). However, these whales tended to
exhibit localized avoidance, remaining significantly further (on
average) from the airgun array during seismic operations compared with
non-seismic periods (Stone and Tasker, 2006). Castellote et al. (2010)
also observed localized avoidance by fin whales during seismic airgun
events in the western Mediterranean Sea and adjacent Atlantic waters
from 2006-2009. They reported that singing fin whales moved away from
an operating airgun array for a time period that extended beyond the
duration of the airgun activity.
Ship-based monitoring studies of baleen whales (including blue,
fin, sei, minke, and whales) in the northwest Atlantic found that
overall, this group had lower sighting rates during seismic versus non-
seismic periods (Moulton and Holst, 2010). Baleen whales as a group
were also seen significantly farther from the vessel during seismic
compared with non-seismic periods, and they were more often seen to be
swimming away from the operating seismic vessel (Moulton and Holst,
2010). Blue and minke whales were initially sighted significantly
farther from the vessel during seismic operations compared to non-
seismic periods; the same trend was observed for fin whales (Moulton
and Holst, 2010). Minke whales were most often observed to be swimming
away from the vessel when seismic operations were underway (Moulton and
Holst, 2010).
Data on short-term reactions by cetaceans to impulsive noises are
not necessarily indicative of long-term or biologically significant
effects. It is not known whether impulsive sounds affect reproductive
rate or distribution and habitat use in subsequent days or years.
However, gray whales have continued to migrate annually along the west
coast of North America with substantial increases in the population
over recent years, despite intermittent seismic exploration (and much
ship traffic) in that area for decades (Appendix A in Malme et al.,
1984; Richardson et al., 1995; Allen and Angliss, 2011). The western
Pacific gray whale population did not seem affected by a seismic survey
in its feeding ground during a previous year (Johnson et al., 2007).
Similarly, bowhead whales have continued to travel to the eastern
Beaufort Sea each summer, and their numbers have increased notably,
despite seismic exploration in their summer and autumn range for many
years (Richardson et al., 1987; Allen and Agliss, 2011).
Toothed Whales--Little systematic information is available about
reactions of toothed whales to noise pulses. Few studies similar to the
more extensive baleen whale/seismic pulse work summarized earlier and
(in more detail) in Appendix B of NSF's EA have been reported for
toothed whales. However, there are recent systematic studies on sperm
whales (e.g., Gordon et al., 2006; Madsen et al., 2006; Winsor and
Mate, 2006; Jochens et al., 2008; Miller et al., 2009). There is 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; Bain and Williams,
2006; Holst et al., 2006; Stone and Tasker, 2006; Potter et al., 2007;
Hauser et al., 2008; Holst and Smultea, 2008; Weir, 2008; Barkaszi et
al., 2009; Richardson et al., 2009; Moulton and Holst, 2010).
Seismic operators and protected species observers (PSOs) on seismic
vessels regularly see dolphins and other small toothed whales near
operating airgun arrays, but in general there is a tendency for most
delphinids to show some avoidance of operating seismic vessels (e.g.,
Goold, 1996a,b,c; Calambokidis and Osmek, 1998; Stone, 2003; Moulton
and Miller, 2005; Holst et al., 2006; Stone and Tasker, 2006; Weir,
2008; Richardson et al., 2009; Barkaszi et al., 2009; Moulton and
[[Page 4773]]
Holst, 2010). 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 (e.g., Moulton and Miller, 2005).
Nonetheless, small toothed whales more often tend to head away, or to
maintain a somewhat greater distance from the vessel, when a large
array of airguns is operating than when it is silent (e.g., Stone and
Tasker, 2006; Weir, 2008; Barry et al., 2010; Moulton and Holst, 2010).
In most cases, the avoidance radii for delphinids appear to be small,
on the order of one km or less, and some individuals show no apparent
avoidance. The beluga whale (Delphinapterus leucas) is a species that
(at least at times) shows long-distance avoidance of seismic vessels.
Summer aerial surveys conducted in the southeastern Beaufort Sea
reported that sighting rates of beluga whales were significantly lower
at distances of 10 to 20 km (6.2 to 12.4 mi) from an operating airgun
array compared to distances of 20 to 30 km (12.4 to 18.6 mi). Further,
PSOs on seismic boats in that area have rarely reported sighting beluga
whales (Miller et al., 2005; Harris et al., 2007).
Captive bottlenose dolphins (Tursiops truncatus) and beluga whales
exhibited changes in behavior when exposed to strong pulsed sounds
similar in duration to those typically used in seismic surveys
(Finneran et al., 2000, 2002, 2005). However, the animals tolerated
high received levels of sound before exhibiting aversive behaviors.
Results for porpoises depend on species. The limited available data
suggest that harbor porpoises (Phocoena phocoena) show stronger
avoidance of seismic operations than do Dall's porpoises (Stone, 2003;
MacLean and Koski, 2005; Bain and Williams, 2006; Stone and Tasker,
2006). Dall's porpoises seem relatively tolerant of airgun operations
(MacLean and Koski, 2005; Bain and Williams, 2006), although they too
have been observed to avoid large arrays of operating airguns
(Calambokidis and Osmek, 1998; Bain and Williams, 2006). This apparent
difference in responsiveness of these two porpoise species is
consistent with their relative responsiveness to boat traffic and some
other acoustic sources (Richardson et al., 1995; Southall et al.,
2007).
Most studies of sperm whales exposed to airgun sounds indicate that
the sperm whale shows considerable tolerance of airgun pulses (e.g.,
Stone, 2003; Moulton et al., 2005, 2006a; Stone and Tasker, 2006; Weir,
2008). In most cases the whales do not show strong avoidance, and they
continue to call (see Appendix B of NSF's EA for review). However,
controlled exposure experiments in the Gulf of Mexico indicate that
foraging behavior was altered upon exposure to airgun sound (Jochens et
al., 2008; Miller et al., 2009; Tyack, 2009).
There are almost no specific data on the behavioral reactions of
beaked whales to seismic surveys. However, some northern bottlenose
whales (Hyperoodon ampullatus) remained in the general area and
continued to produce high-frequency clicks when exposed to sound pulses
from distant seismic surveys (Gosselin and Lawson, 2004; Laurinolli and
Cochrane, 2005; Simard et al., 2005). Most beaked whales tend to avoid
approaching vessels of other types (e.g., Wursig et al., 1998). They
may also dive for an extended period when approached by a vessel (e.g.,
Kasuya, 1986), although it is uncertain how much longer such dives may
be as compared to dives by undisturbed beaked whales, which also are
often quite long (Baird et al., 2006; Tyack et al., 2006). Based on a
single observation, Aguilar-Soto et al. (2006) suggested that foraging
efficiency of Cuvier's beaked whales (Ziphius cavirostris) may be
reduced by close approach of vessels. In any event, it is likely that
most beaked whales would also show strong avoidance of an approaching
seismic vessel, although this has not been documented explicitly. In
fact, Moulton and Holst (2010) reported 15 sightings of beaked whales
during seismic studies in the Northwest Atlantic; seven of those
sightings were made at times when at least one airgun was operating.
There was little evidence to indicate that beaked whale behavior was
affected by airgun operations; sighting rates and distances were
similar during seismic and non-seismic periods (Moulton and Holst,
2010).
There are increasing indications that some beaked whales tend to
strand when naval exercises involving mid-frequency sonar operation are
ongoing nearby (e.g., Simmonds and Lopez-Jurado, 1991; Frantzis, 1998;
NOAA and USN, 2001; Jepson et al., 2003; Hildebrand, 2005; Barlow and
Gisiner, 2006; see also the Stranding and Mortality section in this
notice). These strandings are apparently a disturbance response,
although auditory or other injuries or other physiological effects may
also be involved. Whether beaked whales would ever react similarly to
seismic surveys is unknown. Seismic survey sounds are quite different
from those of the sonar in operation during the above-cited incidents.
Odontocete reactions to large arrays of airguns are variable and,
at least for delphinids and Dall's porpoises, seem to be confined to a
smaller radius than has been observed for the more responsive of the
mysticetes, belugas, and harbor porpoises (See Appendix B of NSF's EA).
Pinnipeds--Pinnipeds are not likely to show a strong avoidance
reaction to the airgun array. Visual monitoring from seismic vessels
has shown only slight (if any) avoidance of airguns by pinnipeds, and
only slight (if any) changes in behavior, see Appendix B(5) of NSF's
EA. In the Beaufort Sea, some ringed seals avoided an area of 100 m
(328 ft) to (at most) a few hundred meters around seismic vessels, but
many seals remained within 100 to 200 m (328 to 656 ft) of the
trackline as the operating airgun array passed by (e.g., Harris et al.,
2001; Moulton and Lawson, 2002; Miller et al., 2005). Ringed seal
sightings averaged somewhat farther away from the seismic vessel when
the airguns were operating than when they were not, but the difference
was small (Moulton and Lawson, 2002). Similarly, in Puget Sound,
sighting distances for harbor seals and California sea lions tended to
be larger when airguns were operating (Calambokidis and Osmek, 1998).
Previous telemetry work suggests that avoidance and other behavioral
reactions may be stronger than evident to date from visual studies
(Thompson et al., 1998).
Hearing Impairment and Other Physical Effects
Exposure to high intensity sound for a sufficient duration may
result in auditory effects such as a noise-induced threshold shift--an
increase in the auditory threshold after exposure to noise (Finneran et
al., 2005). Factors that influence the amount of threshold shift
include the amplitude, duration, frequency content, temporal pattern,
and energy distribution of noise exposure. The magnitude of hearing
threshold shift normally decreases over time following cessation of the
noise exposure. The amount of threshold shift just after exposure is
called the initial threshold shift. If the threshold shift eventually
returns to zero (i.e., the threshold returns to the pre-exposure
value), it is called temporary threshold shift (TTS) (Southall et al.,
2007).
Researchers have studied TTS in certain captive odontocetes and
pinnipeds exposed to strong sounds (reviewed in Southall et al., 2007).
However, there has been no specific documentation of TTS let alone
permanent hearing damage, i.e., permanent threshold shift (PTS), in
free-
[[Page 4774]]
ranging marine mammals exposed to sequences of airgun pulses during
realistic field conditions.
Temporary Threshold Shift--TTS is the mildest form of hearing
impairment that can occur during exposure to a strong sound (Kryter,
1985). While experiencing TTS, the hearing threshold rises and a sound
must be stronger in order to be heard. At least in terrestrial mammals,
TTS can last from minutes or hours to (in cases of strong TTS) days.
For sound exposures at or somewhat above the TTS threshold, hearing
sensitivity in both terrestrial and marine mammals recovers rapidly
after exposure to the noise ends. Few data on sound levels and
durations necessary to elicit mild TTS have been obtained for marine
mammals, and none of the published data concern TTS elicited by
exposure to multiple pulses of sound. Available data on TTS in marine
mammals are summarized in Southall et al. (2007). Table 1 (introduced
earlier in this document) presents the distances from the Langseth's
airguns at which the received energy level (per pulse, flat-weighted)
would be expected to be greater than or equal to 180 dB re: 1 [mu]Pa.
To avoid the potential for injury, NMFS (1995, 2000) concluded that
cetaceans should not be exposed to pulsed underwater noise at received
levels exceeding 180 dB re: 1 [mu]Pa. NMFS believes that to avoid the
potential for permanent physiological damage (Level A harassment),
cetaceans should not be exposed to pulsed underwater noise at received
levels exceeding 180 dB re: 1 [mu]Pa. The 180-dB level is a shutdown
criterion applicable to cetaceans, as specified by NMFS (2000); these
levels were used to establish the EZs. NMFS also assumes that cetaceans
exposed to SPLs exceeding 160 dB re: 1 [mu]Pa may experience Level B
harassment.
Researchers have derived TTS information for odontocetes from
studies on the bottlenose dolphin and beluga. For the one harbor
porpoise tested, the received level of airgun sound that elicited onset
of TTS was lower (Lucke et al., 2009). If these results from a single
animal are representative, it is inappropriate to assume that onset of
TTS occurs at similar received levels in all odontocetes (cf. Southall
et al., 2007). Some cetaceans apparently can incur TTS at considerably
lower sound exposures than are necessary to elicit TTS in the beluga or
bottlenose dolphin.
For baleen whales, there are no data, direct or indirect, on levels
or properties of sound that are required to induce TTS. The frequencies
to which baleen whales are most sensitive are assumed to be lower than
those to which odontocetes are most sensitive, and natural background
noise levels at those low frequencies tend to be higher. As a result,
auditory thresholds of baleen whales within their frequency band of
best hearing are believed to be higher (less sensitive) than are those
of odontocetes at their best frequencies (Clark and Ellison, 2004).
From this, it is suspected that received levels causing TTS onset may
also be higher in baleen whales (Southall et al., 2007). For this
proposed study, L-DEO expects no cases of TTS given the low abundance
of baleen whales in the planned study area at the time of the survey,
and the strong likelihood that baleen whales would avoid the
approaching airguns (or vessel) before being exposed to levels high
enough for TTS to occur.
In pinnipeds, TTS thresholds associated with exposure to brief
pulses (single or multiple) of underwater sound have not been measured.
Initial evidence from more prolonged (nonpulse) exposures suggested
that some pinnipeds (harbor seals in particular) incur TTS at somewhat
lower received levels than do small odontocetes exposed for similar
durations (Kastak et al., 1999, 2005; Ketten et al., 2001). The
indirectly estimated TTS threshold for pulsed sounds would be
approximately 181 to 186 dB re: 1 [mu]Pa (Southall et al., 2007), or a
series of pulses for which the highest SEL values are a few dB lower.
Corresponding values for California sea lions and northern elephant
seals are likely to be higher (Kastak et al., 2005).
Permanent Threshold Shift--When PTS occurs, there is physical
damage to the sound receptors in the ear. In severe cases, there can be
total or partial deafness, whereas in other cases, the animal has an
impaired ability to hear sounds in specific frequency ranges (Kryter,
1985). There is no specific evidence that exposure to pulses of airgun
sound can cause PTS in any marine mammal, even with large arrays of
airguns. However, given the possibility that mammals close to an airgun
array might incur at least mild TTS, there has been further speculation
about the possibility that some individuals occurring very close to
airguns might incur PTS (e.g., Richardson et al., 1995, p. 372ff;
Gedamke et al., 2008). Single or occasional occurrences of mild TTS are
not indicative of permanent auditory damage, but repeated or (in some
cases) single exposures to a level well above that causing TTS onset
might elicit PTS.
Relationships between TTS and PTS thresholds have not been studied
in marine mammals, but are assumed to be similar to those in humans and
other terrestrial mammals. PTS might occur at a received sound level at
least several dBs above that inducing mild TTS if the animal were
exposed to strong sound pulses with rapid rise times-see