Takes of Marine Mammals Incidental to Specified Activities; Three Marine Geophysical Surveys in the Northeast Pacific Ocean, June Through July 2012, 25966-25991 [2012-10627]
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25966
Federal Register / Vol. 77, No. 85 / Wednesday, May 2, 2012 / Notices
Management Act (16 U.S.C. 1855), the
Fish and Wildlife Coordination Act (16
U.S.C. 661), and the National
Environmental Policy Act (42 U.S.C.
4321).
Dated: April 27, 2012.
Brian T. Pawlak,
Acting Director, Office of Habitat
Conservation, National Marine Fisheries
Service.
[FR Doc. 2012–10626 Filed 5–1–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XB105
Takes of Marine Mammals Incidental to
Specified Activities; Three Marine
Geophysical Surveys in the Northeast
Pacific Ocean, June Through July 2012
National Marine Fisheries
Service, National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; proposed incidental
harassment authorization; request for
comments.
AGENCY:
We have received an
application from the Lamont-Doherty
Earth Observatory, a part of Columbia
University, for an Incidental Harassment
Authorization to take marine mammals,
by harassment, incidental to conducting
three consecutive marine geophysical
surveys in the northeast Pacific Ocean,
June through July 2012.
DATES: Comments and information must
be received no later than May 31, 2012.
ADDRESSES: Comments on the
application should be addressed to
Tammy C. Adams, Acting 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.
We are 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 submitted comments are a part of
the public record and we will post 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.
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SUMMARY:
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To obtain an electronic copy of the
application containing a list of the
references used in this document, write
to the previously mentioned address,
telephone the contact listed here (see
FOR FURTHER INFORMATION CONTACT), or
visit the Internet at: https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm#applications.
The National Science Foundation’s
(Foundation) draft Environmental
Assessment (Assessment) pursuant to
the National Environmental Policy Act
of 1969 and Executive Order 12114 is
also available at the same Internet
address. The Assessment incorporates
an ‘‘Environmental Assessment of a
marine geophysical survey by the R/V
Marcus G. Langseth in the northeastern
Pacific Ocean, June–July 2012,’’
prepared by LGL Limited environmental
research associates, on behalf of the
Foundation. The public can view
documents cited in this notice by
appointment, during regular business
hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT:
Jeannine Cody or Howard Goldstein,
National Marine Fisheries Service,
Office of Protected Resources, (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: (1) We make certain findings; (2) the
taking is limited to harassment; and (3)
we provide a notice of a proposed
authorization to the public for review.
We shall grant authorization for the
incidental taking of small numbers of
marine mammals if we find 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. We have
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
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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 Marine
Mammal Protection Act 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
Act establishes a 45-day time limit for
our 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, we must either issue or deny the
authorization and must publish a notice
in the Federal Register within 30 days
of our determination to issue or deny
the authorization.
Except with respect to certain
activities not pertinent here, the Marine
Mammal Protection Act 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
We received an application on
January 27, 2012, from the LamontDoherty Earth Observatory
(Observatory) for the taking by
harassment, of small numbers of marine
mammals, incidental to conducting
three separate marine geophysical
surveys in the northeast Pacific Ocean.
We determined the application
complete and adequate on March 27,
2012.
The Observatory, with research
funding from the U.S. National Science
Foundation (Foundation), plans to
conduct three research studies on the
Juan de Fuca Plate, the Cascadia thrust
zone, and the Cascadia subduction
margin in waters off the Oregon and
Washington coasts. The Observatory has
proposed to conduct the first survey
from June 11 through July 5, 2012, the
second survey from July 5 through July
8, 2012, and the third survey from July
12 through July 23, 2012.
The Observatory plans to use one
source vessel, the R/V Marcus G.
Langseth (Langseth), a seismic airgun
array, a single hydrophone streamer,
and ocean bottom seismometers to
conduct the geophysical surveys.
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The proposed surveys will provide
data necessary to:
• Characterize the evolution and state
of hydration of the Juan de Fuca plate
at the Cascadia subduction zone;
• Provide information on the buried
structures in the region; and
• Assess the location, physical state,
fluid budget, and methane systems of
the Juan de Fuca plate boundary and
overlying crust.
The results of the three studies would
provide background information for
generating improved earthquake hazards
analyses and a better understanding of
the processes that control megathrust
earthquakes which are produced by a
sudden slip along the boundary between
a subducting and an overriding plate.
In addition to the operations of the
seismic airgun array and hydrophone
streamer, and the ocean bottom
seismometers (seismometers), the
Observatory intends to operate a
multibeam echosounder and a subbottom profiler continuously throughout
the surveys.
Acoustic stimuli (i.e., increased
underwater sound) generated during the
operation of the seismic airgun arrays,
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 the Observatory has requested an
authorization to take 26 species of
marine mammals by Level B
harassment. We do not expect that the
use of the multibeam echosounder, the
sub-bottom profiler, or the ocean bottom
seismometer will result in the take of
marine mammals and will discuss our
reasoning later in this notice. Also, we
do not expect take to result from a
collision with the Langseth because it is
a single vessel moving at relatively slow
speeds (4.6 knots (kts); 8.5 kilometers
per hour (km/h); 5.3 miles 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 Activities
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Juan de Fuca Plate Survey
The first proposed seismic survey
would begin on June 11, 2012, and end
on July 5, 2012. The Langseth would
depart from Astoria, Oregon on June 11,
2012, and transit to the survey area in
the northeast Pacific Ocean in
international waters and the Exclusive
Economic Zones of the United States
and Canada. The study area will
encompass an area bounded by
approximately 43–48 degrees (°) North
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by approximately 124–130° East (see
Figure 1 in the Observatory’s
Application #1). Water depths in the
survey area range from approximately
50 to 3,000 meters (m) (164 feet (ft) to
1.9 miles (mi)). At the conclusion of the
first survey, the Langseth would begin a
second three-day seismic survey on July
5, 2012, in the same area.
Typically, two-dimensional surveys
such as this one, acquire data along
single track lines with wide intervals;
cover large areas; provide a coarse
sampled subsurface image; and project
less acoustic energy into the
environment than other types of seismic
surveys. During this survey, the
Langseth would deploy a 36-airgun
array as an energy source, an 8kilometer (km)-long (4.9 mi-long)
hydrophone streamer, and 46
seismometers. The seismometers are
portable, self-contained passive receiver
systems designed to sit on the seafloor
and record seismic signals generated
primarily by airguns and earthquakes.
As the Langseth tows the airgun array
along the survey lines, the hydrophone
streamer receives the returning acoustic
signals and transfers the data to the
vessel’s on-board processing system.
The seismometers also record and store
the returning signals for later analysis.
The Observatory plans to discharge
the airgun array along three long
transect lines and three semi-circular
arcs using the seismometers as the
receivers and then repeat along the long
transect lines in multichannel seismic
mode using the 8-km streamer as the
receiver (see Figure 1 in the
Observatory’s Application #1). Also, the
Observatory will use one support vessel,
the R/V Oceanus (Oceanus) to deploy
46 seismometers on the northern
onshore-offshore line, retrieve the 46
seismometers from the northern line,
and then deploy 39 seismometers on the
southern onshore-offshore lines and
retrieve them at the conclusion of the
survey.
The first study (e.g., equipment
testing, startup, line changes, repeat
coverage of any areas, and equipment
recovery) will require approximately
17 days to complete approximately
3,051 km (1,895.8 mi) of transect lines.
The total survey effort including
contingency will consist of
approximately 2,878 km (1,788.3) of
transect lines in depths greater than
1,000 m (621.3 mi), 102 km (63.4 mi) in
depths 100 to 1,000 m (328 to 3,280 ft),
and 71 km (44.1 mi) in water depths less
than 100 m (328 ft). The northern and
southern onshore-offshore lines are 70
to 310 km (43.4 to 192.6 mi) and 15 to
450 km (9.3 to 279.6 mi) from shore,
respectively.
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Data acquisition will include
approximately 408 hours of airgun
operations (i.e., 17 days over 24 hours).
The Observatory, the Langseth’s
operator, will conduct all planned
seismic activities, with on-board
assistance by the scientists who have
proposed the study. The Principal
Investigators for the survey are Drs. S.
Carbotte and H. Carton (Lamont Doherty
Earth Observatory, New York) and P.
Canales (Woods Hole Oceanographic
Institution, Massachusetts). The vessel
is self-contained and the crew will live
aboard the vessel for the entire cruise.
Cascadia Thrust Zone Survey
The second proposed survey would
begin on July 5, 2012, and end on July
8, 2012. The survey would take place in
the U.S. Exclusive Economic Zone in
waters off of the Oregon and
Washington coasts. The study area will
encompass an area bounded by
approximately 43.5–47° North by
approximately 124–125° East (see Figure
1 in the Observatory’s Application #2).
Water depths in the survey area range
from approximately 50 to 1,000 m (164
ft to 0.62 mi). At the conclusion of this
survey, the Langseth would return to
Astoria, Oregon on July 8, 2012.
The Langseth would deploy a 36airgun array as an energy source, 12
seismometers, and 48 seismometers
(33 in Oregon and 15 in Washington)
onshore (on land). As stated previously,
as the Langseth tows the airgun array
along the survey lines, the seismometers
record the returning acoustic signals for
later analysis. The Observatory proposes
to use the Oceanus to deploy and
retrieve the seismometers.
The Observatory plans to discharge
the airgun array along a grid of lines off
Oregon and along an onshore-offshore
line off Washington (see Figure 1 in the
Observatory’s Application #2).
The proposed study (e.g., equipment
testing, startup, line changes, repeat
coverage of any areas, and equipment
recovery) will require approximately 3
days to complete approximately 793 km
(492.7 mi) of transect lines. The total
survey effort including contingency will
consist of approximately 5 km (3.1 mi)
of transect lines in depths greater than
1,000 m (621.3 mi), 501 km (311.3 mi)
in depths 100 to 1,000 m (328 to 3,280
ft), and 287 km (178.3 mi) in water
depths less than 100 m (328 ft). The
northern and southern legs of the
onshore-offshore lines are 15 to 70 km
(9.3 to 43.5 mi) and 15 to 50 km (9.3 to
31.1 mi) from shore, respectively.
Data acquisition will include
approximately 72 hours of airgun
operations (i.e., 3 days over 24 hours).
The Principal Investigators for the
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second survey are Drs. A.M Trehu
(Oregon State University) and G. Abers
and H. Carton (Lamont Doherty Earth
Observatory, New York). The vessel is
self-contained and the crew will live
aboard the vessel for the entire cruise.
Cascadia Subduction Margin Survey
The last seismic survey would begin
on July 12, 2012, and end on July 23,
2012. The Langseth would depart from
Astoria, Oregon on July 12, 2012, and
transit to waters off of the Washington
coast. The study area encompasses an
area bounded by approximately 46.5–
47.5° North by approximately 124.5–
126° East (see Figure 1 in the
Observatory’s Application #3). Water
depths in the survey area range from
approximately 95 to 2,650 m (311.7 ft to
1.6 mi). At the conclusion of this
survey, the Langseth would return to
Astoria, Oregon on July 23, 2012.
The Langseth would deploy a 36airgun array as an energy source and an
8-km-long (4.9 mi-long) hydrophone
streamer. The Observatory plans to
discharge the airgun array along nine
parallel lines that are spaced eight km
apart. If time permits, the Langseth
would survey an additional two lines
perpendicular to the parallel lines (see
Figure 1 in the Observatory’s
Application #3).
The proposed study (e.g., equipment
testing, startup, line changes, repeat
coverage of any areas, and equipment
recovery) will require approximately 10
days to complete approximately 1,147
km (712.7 mi) of transect lines. The total
survey effort including contingency will
consist of approximately 785 km (487.8
mi) of transect lines in depths greater
than1,000 m (621.3 mi), 350 km (217.5
mi) of transect lines in depths 100 to
1,000 m (328 to 3,280 ft), and 12 km (7.5
mi) of transect lines in water depths less
than 100 m (328 ft). The survey area is
32 to 150 km (19.9 to 93.2 mi) from
shore.
Data acquisition will include
approximately 240 hours of airgun
operations (i.e., 10 days over 24 hours).
The Principal Investigators for the third
survey are Drs. W.S. Holbrook
(University of Wyoming), A.M. Trehu
(Oregon State University), H.P. Johnson
(University of Washington), G.M. Kent
(University of Nevada), and K. Keranen
(University of Oklahoma). The vessel is
self-contained and the crew will live
aboard the vessel for the entire cruise.
Vessel Specifications
The Langseth, owned by the
Foundation, is a seismic research vessel
with a quiet propulsion system that
avoids interference with the seismic
signals emanating from the airgun array.
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The vessel is 71.5 m (235 ft) long; has
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. It’s two 3,550
horsepower (hp) Bergen BRG–6 diesel
engines 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
operational 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 during the first and last
surveys, 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 (observer) will watch
for marine mammals before and during
the proposed airgun operations. When
stationed on the observation platform,
the observer’s eye level will be
approximately 21.5 m (71 ft) above sea
level providing the observer an
unobstructed view around the entire
vessel.
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, we propose to
issue an authorization to the
Observatory that would be effective
from June 9, 2012, to August 27, 2012.
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, 12, or 15 m (29.5,
39.4, or 49.2 ft). The airguns are a
mixture of Bolt 1500LL 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 Langseth’s crew will space
the first and last airguns 16 m (52 ft)
apart from one another. Of the 10
airguns, nine will fire simultaneously
while the tenth airgun will serve as a
spare. The crew will turn on the spare
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airgun in case one of the other airguns
fail. The Langseth will distribute the
array across an area of approximately 24
by 16 m (78.7 by 52.5 ft) and will tow
the array approximately 100 m (328 ft)
behind the vessel.
Juan de Fuca Plate Survey: This
survey’s array tow depth will be 9 m
(29.5 ft) for the multichannel seismic
survey using the hydrophone streamer
and 12 m (39.4 ft) during the survey
using the seismometers. During the
multichannel seismic survey, each
airgun array will emit a pulse at
approximately 16-second (s) intervals
which corresponds to a shot interval of
approximately 37.5 m (123 ft). During
the survey using the seismometers, each
airgun array will emit a pulse at
approximately 200-s intervals which
corresponds to a shot interval of
approximately 500 m (1,640.4 ft).
During firing, the airguns will emit a
brief (approximately 0.1 s) pulse of
sound; during the intervening periods of
operations, the airguns are silent.
Cascadia Thrust Zone Survey: The
survey’s array tow depth will be 12 m
(39.4 ft). During this survey, each airgun
array will emit a pulse at approximately
40-s intervals which corresponds to a
shot interval of approximately 100 m
(328 ft). During firing, the airguns will
emit a brief (approximately 0.1 s) pulse
of sound; during the intervening periods
of operations, the airguns are silent.
Cascadia Subduction Margin Survey:
The survey’s array tow depth will be 15
m (49.2 ft). During this survey, each
airgun array will emit a pulse at
approximately 20-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 are 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. In this document, we
express sound pressure level as the ratio
of a measured sound pressure and a
reference level. The commonly used
reference pressure level in underwater
acoustics is 1 FPa, and the units for
sound pressure levels are dB re: 1 mPa.
Sound pressure level (in decibels (dB))
= 20 log (pressure/reference
pressure)
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Sound pressure level is an
instantaneous measurement and can be
expressed as the peak, the peak-peak (pp), or the root mean square. 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 sound pressure level in
this document refer to the root mean
square unless otherwise noted. Sound
pressure level 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
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 the Observatory on
the Langseth is 236 to 265 dB re: 1
mPa(p-p) and the root mean square 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 root mean square 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, the Observatory has
predicted the received sound levels in
relation to distance and direction from
the 36-airgun array and the single Bolt
1900LL 40-in3 airgun, which will be
used during power downs. Appendix A
of the Foundation’s Environmental
Assessment provides a detailed
description of the modeling for marine
seismic source arrays for species
mitigation and Appendix B(3) of the
Assessment discusses the characteristics
of the airgun pulses. These are the
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. Refer to the
authorization application and
Assessment 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.
The Observatory used the results from
the Gulf of Mexico study to determine
the algorithm for its model that
calculates the exclusion zones for the
36-airgun array and the single airgun.
These values designate mitigation zones
and the Observatory uses them to
estimate take (described in greater detail
in Section VII of the application and
Section IV of the Foundation’s
Environmental Assessment) for marine
mammals.
Comparison of the Tolstoy et al.
(2009) calibration study with the
Observatory’s model for the Langseth’s
36-airgun array indicated that the model
represents the actual received levels,
within the first few kilometers and the
locations of the predicted exclusions
zones. 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
depths in the proposed surveys (9, 12,
or 15 m; 29.5, 39.4, or 49.2 ft), the
Observatory used the following
correction factors for estimating the
received levels during the proposed
surveys (see Table 1). The correction
factors are 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, 12, or
15 m (29.5, 39.4, or 49.2 ft) (LGL, 2008).
TABLE 1—CORRECTION FACTORS FOR
ESTIMATING THE RECEIVED LEVELS
FOR THREE PROPOSED SURVEYS IN
THE NORTHEAST PACIFIC OCEAN,
DURING JUNE–JULY 2012
Array tow depth
160-dB
180-dB
190-dB
9 ........................
12 ......................
15 ......................
1.285
1.467
1.647
1.338
1.577
1.718
1.364
1.545
1.727
For a single airgun, the tow depth has
minimal effect on the maximum nearfield output and the shape of the
frequency spectrum for the single
airgun; thus, the predicted exclusion
zones are essentially the same at
different tow depths. The Observatory’s
model does not allow for bottom
interactions, and thus is most directly
applicable to deep water.
Table 2 summarizes the predicted
distances at which one would expect to
receive three sound levels (160-, 180-,
and 190-dB) from the 36-airgun array
and a single airgun. To avoid the
potential for injury or permanent
physiological damage (Level A
harassment), we (NMFS, 1995, 2000),
we have concluded that cetaceans and
pinnipeds should not be exposed to
pulsed underwater noise at received
levels exceeding 180 dB re: 1 mPa and
190 dB re: 1 mPa, respectively. The 180dB and 190-dB level shutdown criteria
are applicable to cetaceans and
pinnipeds, respectively, specified by us
(NMFS, 1995, 2000). The Observatory
used these levels to establish the
exclusion zones. We also assume that
marine mammals exposed to levels
exceeding 160 dB re: 1 mPa may
experience Level B harassment.
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TABLE 2—MEASURED (ARRAY) OR PREDICTED (SINGLE AIRGUN) DISTANCES TO WHICH SOUND LEVELS GREATER THAN
OR EQUAL TO 160, 180, AND 190 DB RE: 1 μPa THAT COULD BE RECEIVED DURING THE THREE PROPOSED SURVEYS IN THE NORTHEAST PACIFIC OCEAN, DURING JUNE–JULY 2012
Tow depth
(m)
Source and volume (in3)
Single Bolt airgun (40 in3) ..................................................................................
1 6–15
36-Airgun Array (6,600 in3) ................................................................................
9
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Water depth
(m)
Predicted RMS distances 2 (m)
160 dB
>1,000 .........
100 to 1,000
<100 ............
>1,000 .........
100 to 1,000
<100 ............
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385
578
1,050
3,850
12,200
20,550
180 dB
40
60
296
940
1,540
2,140
190 dB
12
18
150
400
550
680
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Federal Register / Vol. 77, No. 85 / Wednesday, May 2, 2012 / Notices
TABLE 2—MEASURED (ARRAY) OR PREDICTED (SINGLE AIRGUN) DISTANCES TO WHICH SOUND LEVELS GREATER THAN
OR EQUAL TO 160, 180, AND 190 DB RE: 1 μPa THAT COULD BE RECEIVED DURING THE THREE PROPOSED SURVEYS IN THE NORTHEAST PACIFIC OCEAN, DURING JUNE–JULY 2012—Continued
Tow depth
(m)
Source and volume (in3)
36-Airgun Array (6,600 in3) ................................................................................
12
36-Airgun Array (6,600 in3) ................................................................................
15
Water depth
(m)
Predicted RMS distances 2 (m)
160 dB
>1,000 .........
100 to 1,000
<100 ............
>1,000 .........
100 to 1,000
<100 ............
4,400
13,935
23,470
4,490
15,650
26,350
180 dB
1,100
1,810
2,250
1,200
1,975
2,750
190 dB
460
615
770
520
690
865
1 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 exclusion zones are essentially the same at different tow depths.
2 The Observatory has based the radii for the array on data in Tolstoy et al. (2009) and has corrected for tow depth using modeled results.
They have based the predicted radii for a single airgun upon their model (see Figure 3 in application #1).
Ocean Bottom Seismometers
The Observatory proposes to use the
Woods Hole Oceanographic Institution
‘‘D2’’ seismometer during the cruise.
The seismometer is approximately one
meter in height and has a maximum
diameter of 50 centimeters (cm). The
anchor (2.5 x 30.5 x 38.1 cm) is hotrolled steel and weighs 23 kilograms.
The acoustic release transponder,
located on the vessel, communicates
with the seismometer at a frequency of
9 to 11 kilohertz (kHz). The source level
of the release signal is 190 dB re: 1 mPa.
The received signal activates the
seismometer’s burn-wire release
assembly which then releases the
seismometer from the anchor. The
seismometer then floats to the ocean
surface for retrieval by the Oceanus.
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Multibeam Echosounder
The Langseth will operate a
Kongsberg EM 122 multibeam
echosounder concurrently during airgun
operations to map characteristics of the
ocean floor. The hull-mounted
echosounder emits brief pulses of sound
(also called a ping) (10.5 to 13 kHz) in
a fan-shaped beam that extends
downward and to the sides of the ship.
The transmitting beamwidth is 1 or 2°
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
milliseconds (ms) in duration and each
ensonifying a sector that extends 1° foreaft. Continuous wave pulses increase
from 2 to 15 ms long in water depths up
to 2,600 m (8,530 ft). The echosounder
uses frequency-modulated chirp pulses
up to 100-ms long in water greater than
2,600 m (8,530 ft). The successive
transmissions span an overall cross-
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track angular extent of about 150°, with
2-ms gaps between the pulses for
successive sectors.
Sub-Bottom Profiler
The Langseth will also operate a
Knudsen Chirp 3260 sub-bottom profiler
concurrently during airgun and
echosounder operations to provide
information about the sedimentary
features and bottom topography. The
profiler is capable of reaching depths of
10,000 m (6.2 mi). The dominant
frequency component is 3.5 kHz and a
hull-mounted transducer on the vessel
directs the beam downward in a 27°
cone. The power output is 10 kilowatts
(kW), but the actual maximum radiated
power is three kilowatts 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.
We expect 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. We also
expect these disturbances to be
temporary and result in a temporary
modification in behavior and/or lowlevel physiological effects (Level B
harassment only) of small numbers of
certain species of marine mammals.
We do 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-one marine mammal species
under our jurisdiction may occur in the
proposed survey areas, including 19
odontocetes (toothed cetaceans), seven
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mysticetes (baleen whales), and five
species of pinniped during June through
July, 2012. Six of these species and two
stocks 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; the
southern resident stock of killer
(Orcinus orca) whales; and the eastern
U.S. stock of the Steller sea lion
(Eumetopias jubatus).
The U.S. Fish and Wildlife Service
manages the northern sea otter (Enhydra
lutis) (listed under the Endangered
Species Act). Because this species is not
under our jurisdiction, we do not
consider this species further in this
notice.
Based on available data, the
Observatory does not expect to
encounter five of the 31 species in the
proposed survey areas. They include
the: the north Pacific right, false killer
(Pseudorca crassidens), and shortfinned pilot (Globicephala
macrorhynchus) whales; the California
sea lion (Zalophus californianus); and
the bottlenose dolphin (Tursiops
truncatus) because of these species’ rare
and/or extralimital occurrence in the
survey areas. Accordingly, we did not
consider these species in greater detail
and the proposed authorization will
only address requested take
authorizations for 26 species: Six
mysticetes, 16 odontocetes, and four
species of pinniped.
Of these 26 species, the most common
marine mammals in the survey area
would be the: harbor porpoise
(Phocoena phocoena), Dall’s porpoise
(Phocoenoides dalli), northern fur seal
(Callorhinus ursinus), and northern
elephant seal (Mirounga angustirostris).
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Table 3 presents information on the
abundance, distribution, and
conservation status of the marine
mammals that may occur in the
proposed survey area June through July
2012.
TABLE 3—HABITAT, ABUNDANCE, DENSITY, AND ESA STATUS OF MARINE MAMMALS THAT MAY OCCUR IN OR NEAR THE
PROPOSED SEISMIC SURVEY AREAS IN THE NORTHEAST PACIFIC OCEAN
[See text and Tables 2 and 3 in the Observatory’s applications and the Foundation’s Environmental Assessment for further details.]
Species
Occurrence
in area
Habitat
Mysticetes
North Pacific right whale ......................................
Gray whale ...........................................................
Humpback whale .................................................
Rare ......................
Common * .............
Common * .............
Coastal, shelf, offshore
Coastal, shallow shelf ..
Mainly nearshore and
banks.
Nearshore, offshore .....
Mostly pelagic ..............
Slope, pelagic ..............
Pelagic and coastal ......
Rare ......................
Rare ......................
Common ...............
Rare ......................
Pygmy sperm whale ............................................
Dwarf sperm whale ..............................................
Cuvier’s beaked whale .........................................
Baird’s beaked whale ...........................................
Blainville’s beaked whale .....................................
Hubb’s beaked whale ..........................................
Stejneger’s beaked whale ....................................
Common bottlenose dolphin ................................
Striped dolphin .....................................................
Short-beaked common dolphin ............................
Pacific white-sided dolphin ..................................
Northern right whale dolphin ................................
Risso’s dolphin .....................................................
False killer whale .................................................
Killer whale ...........................................................
Short-finned pilot whale .......................................
Harbor porpoise ...................................................
Rare ......................
Rare ......................
Common ...............
Common ...............
Rare ......................
Rare ......................
Common ...............
Rare ......................
Rare ......................
Common ...............
Abundant ..............
Common ...............
Common ...............
Rare ......................
Common ...............
Rare ......................
Abundant ..............
Dall’s porpoise .....................................................
Pinnipeds
Northern fur seal ..................................................
California sea lion ................................................
Steller sea lion .....................................................
Harbor seal ..........................................................
Northern elephant seal ........................................
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Minke whale .........................................................
Sei whale .............................................................
Fin whale ..............................................................
Blue whale ...........................................................
Odontocetes
Sperm whale ........................................................
Abundant ..............
Common ...............
Common ...............
Rare ......................
Common * .............
Abundant * ............
Common ...............
Pelagic, steep topography.
Deep, off shelf ..............
Deep, shelf, slope ........
Pelagic .........................
Pelagic .........................
Pelagic .........................
Slope, offshore .............
Slope, offshore .............
Coastal, shelf, deep .....
Off continental shelf .....
Shelf, pelagic, mounts
Offshore, slope .............
Slope, offshore waters
Shelf, slope, mounts ....
Pelagic .........................
Widely distributed .........
Pelagic, high-relief .......
Coastal and inland
waters.
Shelf, slope, offshore ...
Pelagic, offshore ..........
Coastal, shelf ...............
Coastal, shelf ...............
Coastal .........................
Coastal, pelagic in migration.
Abundance
in the
NW Pacific 1
4 31
ESA 2
Density 3
#/1,000 km 2
EN
DL
EN
0
3.21
0.81
2,497
NL
EN
EN
EN
0.46
0.16
1.29
0.18
10 24,000
EN
1.02
5 19,126
6 20,800
7 9,000
8 12,620
9 13,620–18,680
N.A.
N.A.
2,143
907
11 1,024
11 1,024
11 1,024
12 1,006
10,908
411,211
26,930
8,334
6,272
N.A.
2,250–2,700
760
13 55,255
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL/EN 13
NL
NL
0.71
0.71
0.43
1.18
1.75
1.75
1.75
0
0.04
10.28
34.91
12.88
11.19
0
1.66
0
632.4
42,000
NL
83.82
5 653,171
NL
NL
T
NL
NL
83.62
0
13.12
292.3
45.81
296,750
5 58,334–72,223
14 24,732
15 124,000
N.A.—Data not available or species status was not assessed.
* In nearshore survey areas, rare elsewhere.
1 Abundance given for the California/Oregon/Washington or Eastern North Pacific stock (Carretta et al. 2011a,b), unless otherwise stated.
2 Endangered Species Act: EN = Endangered, T = Threatened, DL = Delisted, NL = Not listed.
3 Density estimate as listed in Table 3 of the Observatory’s applications. Refer to pg. 48 of application #1, pg. 47 of application #2, and pg. 47
of application #3 for specific references.
4 Bering Sea (Wade et al. 2010).
5 Eastern North Pacific (Allen and Angliss 2011).
6 North Pacific (Barlow et al. 2009).
7 North Pacific (Wada 1976).
8 North Pacific (Tillman 1977).
9 North Pacific (Ohsumi and Wada 1974).
10 Eastern Temperate North Pacific (Whitehead 2002a).
11 All mesoplodont whales.
12 Offshore stock (Carretta et al. 2011a).
13 The Eastern North Pacific Southern Resident Stock of killer whales is listed as Endangered under the ESA.
14 Northern Oregon/Washington Coast and Northern California/Southern Oregon stocks.
15 Oregon/Washington Coastal Stock (Carretta et al. 2011a).
Refer to Sections III and IV of the
Observatory’s applications for detailed
information regarding the abundance
and distribution, population status, and
life history and behavior of these
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species and their occurrence in the
proposed project area. The applications
also present how the Observatory
calculated the estimated densities for
the marine mammals in the proposed
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survey area. We have reviewed these
data and determined them to be the best
available scientific information for the
purposes of the proposed incidental
harassment authorization.
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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 is not an injury (Southall
et al., 2007). Although we cannot
exclude the possibility entirely, 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 in
this document, we expect some
behavioral disturbance, but we expect
the disturbance to be localized.
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Tolerance
Studies on marine mammals’
tolerance to sound in the natural
environment are relatively rare.
Richardson et al. (1995) defined
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 the
Environmental Assessment). 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)
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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).
We expect that the masking effects of
pulsed sounds (even from large arrays of
airguns) on marine mammal calls and
other natural sounds will be limited,
although there are very few specific data
on this. Because of the intermittent
nature and low duty cycle of seismic
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. We understand that some baleen
and toothed whales continue calling in
the presence of seismic pulses, and that
some researchers have heard these calls
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
have 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). Several
studies have reported hearing dolphins
and porpoises calling while airguns
were operating (e.g., Gordon et al., 2004;
Smultea et al., 2004; Holst et al., 2005a,
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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, we expect that the masking
effects of seismic pulses will be minor,
given the normally intermittent nature
of seismic pulses. Refer to Appendix
B(4) of the Foundation’s Assessment 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 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. There
are less detailed data 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
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Federal Register / Vol. 77, No. 85 / Wednesday, May 2, 2012 / Notices
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 Foundation’s
Assessment, 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 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
(2.5 to 9.3 mi) 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 the Foundation’s
Assessment 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)
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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
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).
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25973
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 the
Foundation’s Assessment). 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).
A few studies have documented
reactions of migrating and feeding (but
not wintering) gray whales to seismic
surveys. 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 feeding at an average received
pressure level of 173 dB re: 1 mPa on an
(approximate) root mean square 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).
Occasionally, observers have seen
various species of Balaenoptera (blue,
sei, fin, and minke whales) in areas
ensonified by airgun pulses (Stone,
2003; MacLean and Haley, 2004; Stone
and Tasker, 2006), and have localized
calls from blue and fin whales 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
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(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. We do
not know 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 appear
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
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(Richardson et al., 1987; Allen and
Angliss, 2011).
Toothed Whales—There is little
systematic information available about
reactions of toothed whales to noise
pulses. There are few studies on toothed
whales similar to the more extensive
baleen whale/seismic pulse work
summarized earlier in Appendix B of
the Foundation’s Assessment. 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 (observers) 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
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, observers on
seismic boats in that area have rarely
reported sighting beluga whales (Miller
et al., 2005; Harris et al., 2007).
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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 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 the
Foundation’s Assessment 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
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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 underway
within the vicinity of the animals (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 abovecited 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 the
Foundation’s Assessment).
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)(3) of the
Foundation’s Assessment. 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
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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 (Southall et al., 2007).
Researchers have studied temporary
threshold shift in certain captive
odontocetes and pinnipeds exposed to
strong sounds (reviewed in Southall et
al., 2007). However, there has been no
specific documentation of temporary
threshold shift let alone permanent
hearing damage, i.e., permanent
threshold shift, in free-ranging marine
mammals exposed to sequences of
airgun pulses during realistic field
conditions.
Temporary Threshold Shift—This is
the mildest form of hearing impairment
that can occur during exposure to a
strong sound (Kryter, 1985). While
experiencing temporary threshold shift,
the hearing threshold rises and a sound
must be stronger in order to be heard.
At least in terrestrial mammals,
temporary threshold shift can last from
minutes or hours to (in cases of strong
shifts) days. For sound exposures at or
somewhat above the temporary
threshold shift threshold, hearing
sensitivity in both terrestrial and marine
mammals recovers rapidly after
exposure to the noise ends. There are
few data on sound levels and durations
necessary to elicit mild temporary
threshold shift for marine mammals,
and none of the published data focus on
temporary threshold shift elicited by
exposure to multiple pulses of sound.
Southall et al. (2007) summarizes
available data on temporary threshold
shift in marine mammals. Table 2
(introduced earlier in this document)
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25975
presents the estimated distances from
the Langseth’s airguns at which the
received energy level (per pulse, flatweighted) would be greater than or
equal to 180 or 190 dB re: 1 mPa.
Researchers have derived temporary
threshold shift 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 temporary threshold shift was lower
(Lucke et al., 2009). If these results from
a single animal are representative, it is
inappropriate to assume that onset of
temporary threshold shift occurs at
similar received levels in all
odontocetes (cf. Southall et al., 2007).
Some cetaceans apparently can incur
temporary threshold shift at
considerably lower sound exposures
than are necessary to elicit temporary
threshold shift 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
temporary threshold shift. 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 temporary
threshold shift onset may also be higher
in baleen whales (Southall et al., 2007).
For this proposed study, the
Observatory expects no cases of
temporary threshold shift 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
temporary threshold shift to occur.
In pinnipeds, researchers have not
measured temporary threshold shift
thresholds associated with exposure to
brief pulses (single or multiple) of
underwater sound. Initial evidence from
more prolonged (non-pulse) exposures
suggested that some pinnipeds (harbor
seals in particular) incur temporary
threshold shift 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 temporary threshold shift
threshold for pulsed sounds would be
approximately 181 to 186 dB re: 1 mPa
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(Southall et al., 2007), or a series of
pulses for which the highest sound
exposure level values are a few decibels
lower. Corresponding values for
California sea lions and northern
elephant seals are likely to be higher
(Kastak et al., 2005).
Permanent Threshold Shift—When
permanent threshold shift 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 permanent threshold shift 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
temporary threshold shift, there has
been further speculation about the
possibility that some individuals
occurring very close to airguns might
incur permanent threshold shift (e.g.,
Richardson et al., 1995, p. 372ff;
Gedamke et al., 2008). Single or
occasional occurrences of mild
temporary threshold shift are not
indicative of permanent auditory
damage, but repeated or (in some cases)
single exposures to a level well above
that causing temporary threshold shift
onset might elicit permanent threshold
shift.
Relationships between temporary
threshold shift and permanent threshold
shift thresholds have not been studied
in marine mammals, but are assumed to
be similar to those in humans and other
terrestrial mammals. Permanent
threshold shift might occur at a received
sound level at least several decibels
above that inducing mild temporary
threshold shift if the animal were
exposed to strong sound pulses with
rapid rise times—see Appendix B(6) of
the Foundation’s Assessment. Based on
data from terrestrial mammals, a
precautionary assumption is that the
permanent threshold shift threshold for
impulse sounds (such as airgun pulses
as received close to the source) is at
least six decibels higher than the
temporary threshold shift threshold on
a peak-pressure basis, and probably
greater than six decibels (Southall et al.,
2007).
Given the higher level of sound
necessary to cause permanent threshold
shift as compared with temporary
threshold shift, it is considerably less
likely that permanent threshold shift
would occur. Baleen whales generally
avoid the immediate area around
operating seismic vessels, as do some
other marine mammals.
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Stranding and Mortality
When a living 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’’.
Marine mammals are known to strand
for a variety of reasons, such as
infectious agents, biotoxicosis,
starvation, fishery interaction, ship
strike, unusual oceanographic or
weather events, sound exposure, or
combinations of these stressors
sustained concurrently or in series.
However, the cause or causes of most
strandings are unknown (Geraci et al.,
1976; Eaton, 1979; Odell et al., 1980;
Best, 1982). Numerous studies suggest
that the physiology, behavior, habitat
relationships, age, or condition of
cetaceans may cause them to strand or
might pre-dispose them to strand when
exposed to another phenomenon. These
suggestions are consistent with the
conclusions of numerous other studies
that have demonstrated that
combinations of dissimilar stressors
commonly combine to kill an animal or
dramatically reduce its fitness, even
though one exposure without the other
does not produce the same result
(Chroussos, 2000; Creel, 2005; DeVries
et al., 2003; Fair and Becker, 2000; Foley
et al., 2001; Moberg, 2000; Relyea,
2005a; 2005b; Romero, 2004; Sih et al.,
2004).
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
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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 mid-frequency active
sonar use in which exposure to sonar is
believed to have been a contributing
factor to strandings: Greece (1996); the
Bahamas (2000); Madeira (2000); Canary
Islands (2002); and Spain (2006). Refer
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 Observatory’s
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 the Foundation’s
Assessment 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;
(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,
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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,
two Cuvier’s beaked whales stranded in
the Gulf of California, Mexico while the
Observatory’s R/V Maurice Ewing had
been operating a 20-airgun (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 midfrequency 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). We anticipate no
injuries of beaked whales during the
proposed study because of:
(1) The likelihood that any beaked
whales nearby would avoid the
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approaching vessel before being
exposed to high sound levels; and
(2) Differences between the sound
sources operated by the Observatory 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
most baleen whales and some
odontocetes, are especially unlikely to
incur non-auditory physical effects.
Potential Effects of Other Acoustic
Devices
Multibeam Echosounder
The Observatory will operate the
Kongsberg EM 122 multibeam
echosounder from the source vessel
during the planned study. Sounds from
the multibeam echosounder 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
echosounder 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
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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 echosounder 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 temporary threshold
shift.
Navy sonars 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
echosounder. The area of possible
influence of the echosounder 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 the Observatory’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 the animal. The
following section outlines possible
effects of an echosounder on marine
mammals.
Masking—Marine mammal
communications will not be masked
appreciably by the echosounder’s
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
echosounder’s 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
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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 Observatory’s
echosounder, 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
echosounder.
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 echosounder proposed for use by the
Observatory is quite different than sonar
used for navy operations. The
echosounder’s pulse duration is very
short relative to the naval sonar. Also,
at any given location, an individual
marine mammal would be in the
echosounder’s beam for much less time
given the generally downward
orientation of the beam and its narrow
fore-aft beamwidth; navy sonar often
uses near-horizontally-directed sound.
Those factors would all reduce the
sound energy received from the
echosounder relative to that from naval
sonar.
Based upon the best available science,
we believe that the brief exposure of
marine mammals to one pulse, or small
numbers of signals, from the
echosounder is not likely to result in the
harassment of marine mammals.
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Sub-Bottom Profiler
The Observatory will also operate a
sub-bottom profiler from the source
vessel during the proposed survey. The
profiler’s sounds are very short pulses,
occurring for one to four ms once every
second. Most of the energy in the sound
pulses emitted by the profiler 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 a profiler 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 temporary threshold shift.
Masking—Marine mammal
communications will not be masked
appreciably by the profiler’s 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 profiler’s 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 profiler are
likely to be similar to those for other
pulsed sources if received at the same
levels. However, the pulsed signals from
the profiler are considerably weaker
than those from the echosounder.
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
profiler 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 profiler operates
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
mammals would be close enough for
there to be any possibility of effects
from the less intense sounds from the
profiler. Based upon the best available
science, we believe that the brief
exposure of marine mammals to signals
from the profiler is not likely to result
in the harassment of marine mammals.
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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.
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.’’
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
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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
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
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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 we
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, we do
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
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).
The Observatory’s proposed operation
of one vessel for the proposed survey is
relatively small in scale compared to the
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25979
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 the 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; observers
posted during operations scan the ocean
for marine mammals and must report
visual alerts of marine mammal
presence to crew; and the observers
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
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
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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 the Foundation’s
Assessment). 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 sub-lethal
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
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.
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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
the Foundation’s Assessment). 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 temporary
threshold shift 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 temporary
threshold shift (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
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 (i.e., the cutoff
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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;
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
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of the sound stimulus (see Appendix D
of the Foundation’s Assessment).
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.
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Anticipated Effects on Fisheries
It is possible that the Langseth’s
streamer may become entangled with
various types of fishing gear. The
Observatory will employ avoidance
tactics as necessary to prevent conflict.
It is not expected that the Observatory’s
operations will have a significant
impact on fisheries in the western
Pacific Ocean. Nonetheless, the
Observatory 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
vertical or horizontal distribution), as
reported in Slotte et al. (2004).
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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 the
Foundation’s Assessment).
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 in
Appendix E of the Foundation’s
Assessment.
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 sound pressure
level was 157 v 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
depend on numerous aspects of the
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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 under section 101(a)(5)(D)
of the Marine Mammal Protection Act,
we 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.
The Observatory has based the
mitigation measures which they will
implement during the proposed seismic
survey, on the following:
(1) Protocols used during previous
seismic research cruises as approved
by us;
(2) Previous incidental harassment
authorizations applications and
authorizations that we have approved
and authorized; 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, the
Observatory and/or its designees would
implement the following mitigation
measures for marine mammals:
(1) Proposed exclusion zones;
(2) Power down procedures;
(3) Shutdown procedures; and
(4) Ramp-up procedures.
Proposed Exclusion Zones—The
Observatory uses safety radii to
designate exclusion zones and to
estimate take for marine mammals.
Table 2 (presented earlier in this
document) shows the distances at which
one would expect to receive three sound
levels (160-, 180-, and 190-dB) from the
36-airgun array and a single airgun. The
180-dB and 190-dB level shutdown
criteria are applicable to cetaceans and
pinnipeds, respectively, as specified by
us (2000). The Observatory used these
levels to establish the exclusion zones.
If the protected species visual
observer detects marine mammal(s)
within or about to enter the appropriate
exclusion zone, the Langseth crew will
immediately power down the airgun
array, or perform a shutdown if
necessary (see Shut-down Procedures).
Power Down Procedures—A power
down involves decreasing the number of
airguns in use such that the radius of
the 180-dB (or 190-dB) zone is smaller
to the extent that marine mammals are
no longer within or about to enter the
exclusion zone. 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, the Observatory will operate
one airgun (40 in3). 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 observer detects a marine
mammal outside the exclusion zone and
the animal is likely to enter the zone,
the crew will power down the airguns
to reduce the size of the 180-dB
exclusion zone before the animal enters
that zone.
Likewise, if a mammal is already
within the zone when first detected, the
crew will power-down the airguns
immediately. During a power down of
the airgun array, the crew will operate
a single 40-in3 airgun which has a
smaller exclusion zone. If the observer
detects a marine mammal within or near
the smaller exclusion zone around the
airgun (Table 2), the crew will shut
down the single airgun (see next
section).
Shutdown Procedures—The Langseth
crew will shutdown the operating
airgun(s) if a marine mammal is seen
within or approaching the exclusion
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zone for the single airgun. The crew will
implement a shutdown:
(1) If an animal enters the exclusion
zone of the single airgun after the crew
has initiated a power down; or
(2) If an animal is initially seen within
the exclusion zone of the single airgun
when more than one airgun (typically
the full airgun array) is operating.
Considering the conservation status
for north Pacific right whales, the
Langseth crew will shutdown the
airgun(s) immediately in the unlikely
event that this species is observed,
regardless of the distance from the
vessel.
Resuming Airgun Operations After a
Power Down
Following a power-down, the
Langseth crew will not resume full
airgun activity until the marine mammal
has cleared the 180-dB exclusion zone
(see Table 2). The observers will
consider the animal to have cleared the
exclusion zone if:
• The observer has visually observed
the animal leave the exclusion zone, or
• An observer has not sighted the
animal within the exclusion zone for 15
minutes for species with shorter dive
durations (i.e., small odontocetes or
pinnipeds), or 30 minutes 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 transited outside the
original 180-dB exclusion zone after an
8-minute wait period. This period is
based on the 180-dB exclusion zone for
the 36-airgun array (940 m) towed at a
depth of 9 m (29.5 ft) in relation to the
average speed of the Langseth while
operating the airguns (8.5 km/h; 5.3
mph).
The Langseth crew will resume
operating the airguns at full power after
15 minutes of sighting any species with
short dive durations (i.e., small
odontocetes or pinnipeds). Likewise, the
crew will resume airgun operations at
full power after 30 minutes of sighting
any species with longer dive durations
(i.e., mysticetes and large odontocetes,
including sperm, pygmy sperm, dwarf
sperm, and beaked whales).
Because the vessel has transited 1.13
km (3,707 feet) away from the vicinity
of the original sighting during the 8minute period, implementing ramp-up
procedures for the full array after an
extended power down (i.e., transiting
for an additional 35 minutes from the
location of initial sighting) would not
meaningfully increase the effectiveness
of observing marine mammals
approaching or entering the exclusion
zone for the full source level and would
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not further minimize the potential for
take. The Langseth’s observers are
continually monitoring the exclusion
zone for the full source level while the
mitigation airgun is firing. On average,
observers can observe to the horizon (10
km; 6.2 mi) from the height of the
Langseth’s observation deck and should
be able to say with a reasonable degree
of confidence whether a marine
mammal would be encountered within
this distance before resuming airgun
operations at full power.
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Resuming Airgun Operations After a
Shutdown
Following a shutdown, the Langseth
crew will initiate a ramp-up with the
smallest airgun in the array (40-in3). The
crew will turn on additional airguns in
a sequence such that the source level of
the array will increase in steps not
exceeding 6 dB per five-minute period
over a total duration of approximately
30 minutes. During ramp-up, the
observers will monitor the exclusion
zone, and if he/she sights a marine
mammal, the Langseth crew will
implement a power down or shutdown
as though the full airgun array were
operational.
During periods of active seismic
operations, there are occasions when the
Langseth crew will need to temporarily
shut down the airguns due to equipment
failure or for maintenance. In this case,
if the airguns are inactive longer than
eight minutes, the crew will follow
ramp-up procedures for a shutdown
described earlier and the observers will
monitor the full exclusion zone and will
implement a power down or shutdown
if necessary.
If the full exclusion zone is not visible
to the observer for at least 30 minutes
prior to the start of operations in either
daylight or nighttime, the Langseth crew
will not commence 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 the
vessel’s crew will not ramp up the
airgun array from a complete shutdown
at night or in thick fog, because the
outer part of the zone 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. The vessel’s crew will not
initiate a ramp-up of the airguns if a
marine mammal is sighted within or
near the applicable exclusion zones
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during the day or close to the vessel at
night.
We have carefully evaluated the
applicant’s proposed mitigation
measures and have considered a range
of other measures in the context of
ensuring that we have prescribed the
means of effecting the least practicable
adverse impact on the affected marine
mammal species and stocks and their
habitat. Our evaluation of potential
measures included consideration of the
following factors in relation to one
another:
(1) The manner in which, and the
degree to which, we expect that the
successful implementation of the
measure would 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 our evaluation of the
Observatory’s proposed measures, as
well as other measures considered by us
or recommended by the public, we have
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
grounds, and areas of similar
significance.
Proposed Monitoring and Reporting
In order to issue an incidental take
authorization for an activity, section
101(a)(5)(D) of the Marine Mammal
Protection Act states that we must set
forth ‘‘requirements pertaining to the
monitoring and reporting of such
taking.’’ The Act’s implementing
regulations at 50 CFR 216.104(a)(13)
indicate that requests for an
authorization must include the
suggested means of accomplishing the
necessary monitoring and reporting that
will result in increased knowledge of
the species and our expectations of the
level of taking or impacts on
populations of marine mammals present
in the action area.
Proposed Monitoring
The Observatory proposes to sponsor
marine mammal monitoring during the
present project, in order to implement
the mitigation measures that require
real-time monitoring, and to satisfy the
monitoring requirements of the
incidental harassment authorization. We
describe the Observatory’s Monitoring
Plan below this section. The
Observatory understands that this
monitoring plan will be subject to
review by us, and that we may require
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25983
refinements to the plan. The
Observatory has planned the monitoring
work as a self-contained project
independent of any other related
monitoring projects that may occur in
the same regions at the same time.
Further, the Observatory would discuss
coordination of its monitoring program
with any other related work by other
groups working in the same area, if
practical.
Vessel-Based Visual Monitoring
The Observatory will position
observers aboard the seismic source
vessel to watch for marine mammals
near the vessel during daytime airgun
operations and during any start-ups at
night. Observers will also watch for
marine mammals near the seismic
vessel for at least 30 minutes prior to the
start of airgun operations after an
extended shutdown (i.e., greater than
approximately eight minutes for this
proposed cruise). When feasible, the
observers 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 the observations, the
Langseth will power down or shutdown
the airguns when marine mammals are
observed within or about to enter a
designated exclusion zone which is a
region in which a possibility exists of
adverse effects on animal hearing or
other physical effects.
During seismic operations, at least
four protected species observers will be
aboard the Langseth. The Observatory
will appoint the observers with our
concurrence. They will conduct
observations during ongoing daytime
operations and nighttime ramp-ups of
the airgun array. During the majority of
seismic operations, two observers will
be on duty from the observation tower
to monitor marine mammals near the
seismic vessel. Using two observers will
increase the effectiveness of detecting
animals near the source vessel.
However, during mealtimes and
bathroom breaks, it is sometimes
difficult to have two observers on effort,
but at least one observer will be on
watch during bathroom breaks and
mealtimes. Observers will be on duty in
shifts of no longer than four hours in
duration.
Two observers will also be on visual
watch during all nighttime ramp-ups of
the seismic airguns. A third observer
will monitor the passive acoustic
monitoring equipment 24 hours a day to
detect vocalizing marine mammals
present in the action area. In summary,
a typical daytime cruise would have
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scheduled two observers (visual) on
duty from the observation tower, and a
observer (acoustic) on the passive
acoustic monitoring system. Before the
start of the seismic survey, the
Observatory will instruct the vessel’s
crew to assist in detecting marine
mammals and implementing mitigation
requirements.
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
observers will scan the area around the
vessel systematically with reticle
binoculars (e.g., 7 x 50 Fujinon), Big-eye
binoculars (25 x 150), and with the
naked eye. During darkness, night
vision devices 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 observers see marine
mammals within or about to enter the
designated exclusion zone, the Langseth
will immediately power down or
shutdown the airguns if necessary. The
observer(s) will continue to maintain
watch to determine when the animal(s)
are outside the exclusion zone by visual
confirmation. Airgun operations will
not resume until the observer has
confirmed that the animal has left the
zone, or if not observed after 15 minutes
for species with shorter dive durations
(small odontocetes and pinnipeds) or 30
minutes 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 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
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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 acoustic
observer will monitor the system in real
time so that he/she can advise the visual
observers if they acoustic detect
cetaceans. When the acoustic observer
determines the bearing (primary and
mirror-image) to calling cetacean(s), he/
she alert the visual observer to help
him/her sight the calling animal(s).
The passive acoustic monitoring
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). The Langseth
crew 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.
As described earlier, one acoustic
observer, an expert bioacoustician with
primary responsibility for the passive
acoustic monitoring system will be
aboard the Langseth in addition to the
four visual observers. The acoustic
observer will monitor the towed
hydrophones 24 hours per day during
airgun operations and during most
periods when the Langseth is underway
while the airguns are not operating.
However, passive acoustic monitoring
may not be possible if damage occurs to
both the primary and back-up
hydrophone arrays during operations.
The primary passive acoustic
monitoring 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 acoustic observer 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
observer monitoring the acoustical data
will be on shift for one to six hours at
a time. The other observers will rotate
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as an acoustic observer, although the
expert acoustician will be on passive
acoustic monitoring duty more
frequently.
When the acoustic observer detects a
vocalization while visual observations
are in progress, the acoustic observer on
duty will contact the visual observer
immediately, to alert him/her to the
presence of cetaceans (if they have not
already been seen), so that the vessel’s
crew can initiate a power down or
shutdown, if required. The observer will
enter the information regarding the call
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.
Observer Data and Documentation
Observers 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.
They will use the data 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
exclusion zone.
When an observer makes a sighting,
they will record the following
information:
1. Species, group size, age/size/sex
categories (if determinable), behavior
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 observer will record the data
listed under (2) 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.
Observers will record all observations
and power downs or shutdowns in a
standardized format and will enter data
into an electronic database. The
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observers will verify the accuracy of the
data entry by computerized data validity
checks as the data are entered and by
subsequent manual checking of the
database. These procedures will allow
the preparation of initial summaries of
data 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 shutdown).
2. Information needed to estimate the
number of marine mammals potentially
taken by harassment, which the
Observatory must report to the Office of
Protected Resources.
3. Data on the occurrence,
distribution, and activities of marine
mammals and turtles in the area where
the Observatory will conduct the
seismic study.
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
detected during non-active and active
seismic operations.
Proposed Reporting
The Observatory will submit a report
to us and to the Foundation 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
‘‘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 authorization (if
issued), such as an injury (Level A
harassment), serious injury or mortality
(e.g., ship-strike, gear interaction, and/or
entanglement), the Observatory shall
immediately cease the specified
activities and immediately report the
incident to the Incidental Take Program
Supervisor, Permits and Conservation
Division, Office of Protected Resources,
NMFS, at 301–427–8401 and/or by
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email to Jolie.Harrison@noaa.gov and
ITP.Cody@noaa.gov and to the
Northwest Regional Stranding
Coordinator at (206) 526–6550
(Brent.Norberg@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).
The Observatory shall not resume its
activities until we are able to review the
circumstances of the prohibited take.
We shall work with the Observatory to
determine what is necessary to
minimize the likelihood of further
prohibited take and ensure Marine
Mammal Protection Act compliance.
The Observatory may not resume their
activities until notified by us via letter,
email, or telephone.
In the event that the Observatory
discovers an injured or dead marine
mammal, and the lead visual observer
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 we
describe in the next paragraph), the
Observatory will immediately report the
incident to the Incidental Take Program
Supervisor, Permits and Conservation
Division, Office of Protected Resources,
at 301–427–8401 and/or by email to
Jolie.Harrison@noaa.gov and
ITP.Cody@noaa.gov and to the
Northwest Regional Stranding
Coordinator at (206) 526–6550
(Brent.Norberg@noaa.gov). The report
must include the same information
identified in the paragraph above this
section. Activities may continue while
we review the circumstances of the
incident. We will work with the
Observatory to determine whether
modifications in the activities are
appropriate.
In the event that the Observatory
discovers an injured or dead marine
mammal, and the lead visual observer
determines that the injury or death is
not associated with or related to the
authorized activities (e.g., previously
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25985
wounded animal, carcass with moderate
to advanced decomposition, or
scavenger damage), the Observatory will
report the incident to the Incidental
Take Program Supervisor, Permits and
Conservation Division, Office of
Protected Resources, at 301–427–8401
and/or by email to
Jolie.Harrison@noaa.gov and
ITP.Cody@noaa.gov and the Northwest
Regional Stranding Coordinator at (206)
526–6550 (Brent.Norberg@noaa.gov),
within 24 hours of the discovery. The
Observatory will provide photographs
or video footage (if available) or other
documentation of the stranded animal
sighting to us.
Estimated Take by Incidental
Harassment
Except with respect to certain
activities not pertinent here, the Marine
Mammal Protection Act 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].
We propose to authorize take by Level
B harassment only for the proposed
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 re: 1 mPa or
cause temporary, short-term changes in
behavior. There is no evidence that the
Observatory’s planned activities could
result in injury, serious injury or
mortality within the specified
geographic area for the requested
authorization. The required mitigation
and monitoring measures will minimize
any potential risk for injury, serious
injury, or mortality.
The following sections describe the
Observatory’s methods to estimate take
by incidental harassment and present
their estimates of the numbers of marine
mammals that could be affected during
the proposed seismic program. The
Observatory’s estimates assume that
marine mammals exposed to airgun
sounds greater than or equal to 160 dB
re: 1 mPa might change their behavior
sufficiently for us to consider them as
taken by harassment. They have based
their estimates on the number of marine
mammals that could be disturbed
appreciably by operations with the 36-
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airgun array during approximately 4,991
km (3,101.2 mi) of transect lines in the
northeastern Pacific Ocean.
We assume that during simultaneous
operations of the airgun array and the
other sources, any marine mammals
close enough to be affected by the
echosounder and sub-bottom profiler
would already be affected by the
airguns. However, whether or not the
airguns are operating simultaneously
with the other sources, we expect that
the marine mammals would exhibit no
more than short-term and
inconsequential responses to the
echosounder and profiler given their
characteristics (e.g., narrow downwarddirected beam) and other considerations
described previously. Based on the best
available information, we do not
consider that these reactions constitute
a ‘‘take’’ (NMFS, 2001). Therefore, the
Observatory did not provide any
additional allowance for animals that
could be affected by sound sources
other than the airguns.
Ensonified Area Calculations—
Because the Observatory assumes that
the Langseth may need repeat some
tracklines, accommodate the turning of
the vessel, address equipment
malfunctions, or conduct equipment
testing to complete the survey; they
have increased the proposed number of
line-kilometers for the seismic
operations by 25 percent (i.e.,
contingency lines).
The Observatory calculated the
expected ensonified area by entering the
planned survey lines (including the 25
percent contingency lines) into a MapInfo Geographic Information System
(system). The Observatory used the
system to draw a 160-dB radius (see
Table 2) around the operating airgun
array (i.e., the ensonified area) around
each seismic line. This first calculation
is the area excluding overlap.
Depending on the spacing of the
transect lines within the ensonified
area, the Observatory may also calculate
areas of transit overlap. For example, if
the ratio of transit overlap is 1.5 times
the area excluding overlap, then the
marine mammal that stayed within area
during the entire survey could be
exposed to acoustic stimuli
approximately two times. However, it is
unlikely that a particular animal would
stay in the area during the entire survey.
For the Juan de Fuca Survey, the transit
lines are closely spaced together and the
ratio of transect overlap is 1.7 greater
than the area excluding overlapping
transect lines. For the Cascadia Thrust
Zone Survey the ratio is 2.8, and for the
Cascadia Subduction Margin Survey the
ratio is 2.0 times the area excluding
overlap. Table 4 presents the area
calculations for each survey. Refer to the
authorization application and
Assessment for additional information.
TABLE 4—ENSONIFIED AREA CALCULATIONS FOR THREE PROPOSED SEISMIC SURVEYS IN THE NORTHEAST PACIFIC
OCEAN, DURING JUNE–JULY 2012
Area
excluding
overlap
(km2)
Survey
mstockstill on DSK4VPTVN1PROD with NOTICES
Juan de Fuca Plate ............................................................................
Cascadia Thrust Zone .......................................................................
Cascadia Subduction Margin .............................................................
Density Information—The
Observatory calculated the density data
for 26 species reported off the Oregon
and Washington coasts in the
northeastern Pacific Ocean using the
following data sources:
• Pooled results of the 1991–2008
NMFS Southwest Fishery Science
Center ship surveys as synthesized by
Barlow and Forney (2007) and Barlow
(2010) for all species except the gray
whale and harbor porpoise.
• Abundance estimates for gray
whales that remain between Oregon and
B.C. in summer and the within area out
to 43 km (26.7 mi) from shore in the
U.S. Navy’s Keyport Range Complex
Extension Environmental Impact
Statement/Overseas Environmental
Impact Statement (DoN, 2010); and
• The population estimate for the
Northern Oregon/Washington Coast
stock of harbor porpoises from the
Pacific Marine Mammal Stock
Assessments 2010 Report (Carretta et
al., 2010).
For the pooled results of the 1991–
2008 NMFS Southwest Fishery Science
Center ship surveys, the Observatory
has corrected the densities for trackline
detectability probability bias and
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Jkt 226001
18,471
11,448
11,387
Area with
contingency
lines (km2)
23,089
14,310
14,234
availability bias. Trackline detectability
probability 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).
Exposure Calculations—The
Observatory calculated the number of
different individuals that could be
exposed to airgun sounds with received
levels greater than or equal to 160 dB re:
1 mPa by multiplying the expected
density of the marine mammals by the
ensonified area excluding areas of
overlap. This area includes the 25
percent contingency lines.
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
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Transect line spacing
Overlap
ratio
(km2)
Closely spaced ............................
Closely spaced ............................
Closely spaced ............................
1.7
2.8
2.0
mitigation delays, which is highly
unlikely.
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 re: 1 mPa, which
will result in overestimates for those
species known to avoid seismic vessels.
Juan de Fuca Plate Survey Exposure
Estimates
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 this survey is
10,208 (see Table 5). The total includes
78 baleen whales, 56 of which are
endangered: four blue whales (0.17
percent of the regional population), 30
fin whales (0.18 percent of the regional
population), 19 humpback whales (0.09
percent of the regional population), and
four sei whales (0.03 percent of the
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Federal Register / Vol. 77, No. 85 / Wednesday, May 2, 2012 / Notices
Of the cetaceans potentially exposed,
57 percent are delphinids and 42
percent are pinnipeds. The most
common species in the area potentially
exposed to sound levels greater than or
equal to 160 dB re: 1 mPa during the
proposed survey would be harbor
population). In addition, 24 sperm
whales (0.10 percent of the regional
population) and 303 Steller sea lions
(0.46 percent of the population) (both
listed as endangered under the
Endangered Species Act) could be
exposed during the survey.
porpoises (2,153 or 4.12 percent), Dall’s
porpoises (1,935 or 4.61 percent),
northern fur seals (1,931 or 0.30
percent), and northern elephant seals
(1,058 or 0.85 percent).
TABLE 5—ESTIMATES OF THE POSSIBLE NUMBERS OF MARINE MAMMALS EXPOSED TO SOUND LEVELS GREATER THAN
OR EQUAL TO 160 DB RE: 1 μPa DURING THE PROPOSED JUAN DE FUCA PLATE SEISMIC SURVEY IN THE NORTHEAST PACIFIC OCEAN, JUNE–JULY 2012
Estimated
number of
individuals
exposed to
sound levels
≥160 dB re:
1 μPa 1
Species
Gray whale ...................................................................................................................................
Humpback whale .........................................................................................................................
Minke whale .................................................................................................................................
Sei whale .....................................................................................................................................
Fin whale .....................................................................................................................................
Blue whale ...................................................................................................................................
Odontocetes
Sperm whale ................................................................................................................................
Pygmy/Dwarf sperm whale ..........................................................................................................
Cuvier’s beaked whale ................................................................................................................
Baird’s beaked whale ..................................................................................................................
Mesoplodon spp.3 ........................................................................................................................
Striped dolphin .............................................................................................................................
Short-beaked common dolphin ....................................................................................................
Pacific white-sided dolphin ..........................................................................................................
Northern right whale dolphin .......................................................................................................
Risso’s dolphin .............................................................................................................................
Killer whale ..................................................................................................................................
Harbor porpoise 5 .........................................................................................................................
Dall’s porpoise .............................................................................................................................
Pinnipeds
Northern fur seal ..........................................................................................................................
Steller sea lion .............................................................................................................................
Harbor seal 5 ................................................................................................................................
Northern elephant seal ................................................................................................................
Requested or
adjusted take
authorization
Approximate
percent of
regional
population 2
10
19
11
4
30
4
10
19
11
4
30
4
0
0.09
0.12
0.03
0.18
0.17
24
16
10
27
40
1
237
806
297
258
38
2,153
1,935
24
16
10
27
40
42
4 238
806
297
258
38
2,153
1,935
0.10
N/A
0.46
3.0
3.95
0.01
0.06
299
3.57
4.12
1.55
4.12
4.61
1,931
303
995
1,058
1,931
303
995
1,058
0.30
0.46
4.02
0.85
N/A = Not Available
1 Estimates are based on densities in Table 3 and an ensonified area (including 25% contingency of 23,089 km2).
2 Regional population size estimates are from Table 3 (page 48 in Application #1).
3 Includes Blainville’s, Stejneger’s, and Hubb’s beaked whales.
4 Requested take authorization increased to mean group size (see Application #1).
5 Estimates based on densities from Table 3 (page 48 in Application #1) and an ensonified area in water depths less than 100 m (328 ft) (including 25 percent contingency) of 3,404 km.2
mstockstill on DSK4VPTVN1PROD with NOTICES
Cascadia Thrust Zone Survey Exposure
Estimates
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 this survey is
15,100 (see Table 6). The total includes
79 baleen whales, 35 of which are
endangered: Three blue whales (0.10
percent of the regional population), 18
fin whales (0.11 percent of the regional
population), 12 humpback whales (0.06
percent of the regional population), and
two sei whales (0.02 percent of the
population). In addition, 15 sperm
whales (0.06 percent of the regional
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16:55 May 01, 2012
Jkt 226001
population) and 188 Steller sea lions
(0.29 percent of the population) (both
listed as endangered under the
Endangered Species Act) could be
exposed during the survey.
Of the cetaceans potentially exposed,
63 percent are delphinids and 36
percent are pinnipeds. The most
common species in the area potentially
exposed to sound levels greater than or
equal to 160 dB re: 1 mPa during the
proposed survey would be Dall’s
porpoises (1,199 or 2.86 percent), harbor
porpoises (7,314 or 14 percent of the
regional population or 9.2 percent of the
overall population), and harbor seals
(3,380 or 13.67 percent of the regional
population or 4.6% of the overall
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Fmt 4703
Sfmt 4703
population) and northern fur seals
(1,197 or 0.18 percent) (Allen and
Angliss, 2011). The percentages for
harbor porpoises and harbor seals are
the upper boundaries of the regional
populations that could be affected by
the proposed survey. However, these
take estimates are small relative to the
overall population sizes for each species
in the northeast Pacific. Thus, these take
estimates are likely an overestimate of
the actual number of animals that may
be taken by Level B harassment and we
expect that the actual number of
individual animals that may be taken by
Level B harassment to be less than the
request.
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TABLE 6—ESTIMATES OF THE POSSIBLE NUMBERS OF MARINE MAMMALS EXPOSED TO SOUND LEVELS GREATER THAN
OR EQUAL TO 160 DB RE: 1 μPa DURING THE PROPOSED CASCADIA THRUST ZONE SEISMIC SURVEY IN THE NORTHEAST PACIFIC OCEAN, JULY 2012
Estimated
number of
individuals
exposed to
sound levels
≥160 dB re: 1
μPa 1
Species
Requested or
adjusted take
authorization
35
12
7
2
18
3
35
12
7
2
18
3
0.18
0.06
0.07
0.02
0.11
0.10
15
10
6
17
25
1
147
500
184
160
24
7,314
1,199
15
10
6
17
25
42
4 238
500
184
160
24
7,314
1,199
0.06
NA
0.28
1.86
2.45
<0.01
0.04
1.86
2.21
2.55
0.96
14.00
2.86
1,197
188
3,380
656
1,197
188
3,380
656
0.18
0.29
13.67
0.53
Gray whale ...................................................................................................................................
Humpback whale .........................................................................................................................
Minke whale .................................................................................................................................
Sei whale .....................................................................................................................................
Fin whale .....................................................................................................................................
Blue whale ...................................................................................................................................
Odontocetes
Sperm whale ................................................................................................................................
Pygmy/Dwarf sperm whale ..........................................................................................................
Cuvier’s beaked whale ................................................................................................................
Baird’s beaked whale ..................................................................................................................
Mesoplodon spp.3 ........................................................................................................................
Striped dolphin .............................................................................................................................
Short-beaked common dolphin ....................................................................................................
Pacific white-sided dolphin ..........................................................................................................
Northern right whale dolphin .......................................................................................................
Risso’s dolphin .............................................................................................................................
Killer whale ..................................................................................................................................
Harbor porpoise 5 .........................................................................................................................
Dall’s porpoise .............................................................................................................................
Pinnipeds
Northern fur seal ..........................................................................................................................
Steller sea lion .............................................................................................................................
Harbor seal 5 ................................................................................................................................
Northern elephant seal ................................................................................................................
Approximate
percent of
regional
population 2
N/A = Not Available.
1 Estimates are based on densities in Table 3 and an ensonified area (including 25% contingency of 14,310 km2).
2 Regional population size estimates are from Table 3 (page 47 in Application #2).
3 Includes Blainville’s, Stejneger’s, and Hubb’s beaked whales.
4 Requested take authorization increased to mean group size (see Application #2).
5 Estimates based on densities from Table 3 (page 47 in Application #2) and an ensonified area in water depths less than 100 m (328 ft) (including 25 percent contingency) of 11.565 km2.
Cascadia Subduction Margin Survey
Exposure Estimates
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 this survey is
8,132 (see Table 7). The total includes
54 baleen whales, 35 of which are
endangered: three blue whales (0.10
percent of the regional population), 18
fin whales (0.11 percent of the regional
population), 11 humpback whales (0.06
percent of the regional population), and
two sei whales (0.02 percent of the
population). In addition, 15 sperm
whales (0.06 percent of the regional
population) and 187 Steller sea lions
(0.29 percent of the population) (both
listed as endangered under the
Endangered Species Act) could be
exposed during the survey.
Of the cetaceans potentially exposed,
59 percent are delphinids and 40
percent are pinnipeds. The most
common species in the area potentially
exposed to sound levels greater than or
equal to 160 dB re: 1 mPa during the
proposed survey would be harbor
porpoises (2,580 or 4.94 percent), Dall’s
porpoises (1,193 or 2.84 percent),
northern fur seals (1,190 or 0.18
percent), and harbor seals (1,192 or 4.82
percent).
mstockstill on DSK4VPTVN1PROD with NOTICES
TABLE 7—ESTIMATES OF THE POSSIBLE NUMBERS OF MARINE MAMMALS EXPOSED TO SOUND LEVELS GREATER THAN
OR EQUAL TO 160 DB RE: 1 μPa DURING THE PROPOSED CASCADIA SUBDUCTION MARGIN SEISMIC SURVEY IN THE
NORTHEAST PACIFIC OCEAN, JULY 2012
Estimated
number of
individuals
exposed to
sound levels
≥160 dB
re: 1 μPa1
Species
Gray whale ...................................................................................................................................
Humpback whale .........................................................................................................................
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E:\FR\FM\02MYN1.SGM
12
11
02MYN1
Requested or
adjusted take
authorization
12
11
Approximate
percent of
regional
population 2
0.06
0.06
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TABLE 7—ESTIMATES OF THE POSSIBLE NUMBERS OF MARINE MAMMALS EXPOSED TO SOUND LEVELS GREATER THAN
OR EQUAL TO 160 DB RE: 1 μPa DURING THE PROPOSED CASCADIA SUBDUCTION MARGIN SEISMIC SURVEY IN THE
NORTHEAST PACIFIC OCEAN, JULY 2012—Continued
Estimated
number of
individuals
exposed to
sound levels
≥160 dB
re: 1 μPa1
Species
Minke whale .................................................................................................................................
Sei whale .....................................................................................................................................
Fin whale .....................................................................................................................................
Blue whale ...................................................................................................................................
Odontocetes
Sperm whale ................................................................................................................................
Pygmy/Dwarf sperm whale ..........................................................................................................
Cuvier’s beaked whale ................................................................................................................
Baird’s beaked whale ..................................................................................................................
Mesoplodon spp.3 ........................................................................................................................
Striped dolphin .............................................................................................................................
Short-beaked common dolphin ....................................................................................................
Pacific white-sided dolphin ..........................................................................................................
Northern right whale dolphin .......................................................................................................
Risso’s dolphin .............................................................................................................................
Killer whale ..................................................................................................................................
Harbor porpoise 5 .........................................................................................................................
Dall’s porpoise .............................................................................................................................
Pinnipeds
Northern fur seal ..........................................................................................................................
Steller sea lion .............................................................................................................................
Harbor seal 5 ................................................................................................................................
Northern elephant seal ................................................................................................................
Requested or
adjusted take
authorization
Approximate
percent of
regional
population 2
6
2
18
3
6
2
18
3
0.07
0.02
0.11
0.10
15
10
6
17
25
1
146
497
183
159
24
2,580
1,193
15
10
6
17
25
42
4 238
497
183
159
24
2,580
1,193
0.06
NA
0.28
1.85
2.44
<0.01
0.04
1.85
2.20
2.54
0.96
4.94
2.84
1,190
187
1,192
652
1,190
187
1,192
652
0.18
0.29
4.82
0.53
N/A = Not Available.
1 Estimates are based on densities in Table 3 and an ensonified area (including 25% contingency of 14,234 km2).
2 Regional population size estimates are from Table 3 (page 47 in Application #3).
3 Includes Blainville’s, Stejneger’s, and Hubb’s beaked whales.
4 Requested take authorization increased to mean group size (see Application #3).
5 Estimates based on densities from Table 3 (page 47 in Application #3) and an ensonified area in water depths less than 100 m (328 ft) (including 25 percent contingency) of 4,080 km2.
mstockstill on DSK4VPTVN1PROD with NOTICES
Encouraging and Coordinating
Research
The Observatory and the Foundation
will coordinate the planned marine
mammal monitoring program associated
with each seismic survey in the
northwestern Pacific Ocean with other
parties that may have interest in the area
and/or may be conducting marine
mammal studies in the same region
during the seismic surveys.
Negligible Impact and Small Numbers
Analysis and Determination
We have 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, we consider:
(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
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Jkt 226001
(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
surveys are not likely to cause
permanent threshold shift, or other nonauditory injury, serious injury, or death
because:
(1) The likelihood that, given
sufficient notice through relatively slow
ship speed, we expect marine mammals
to move away from a noise source that
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is annoying prior to its becoming
potentially injurious;
(2) The potential for temporary or
permanent hearing impairment is
relatively low and that we would likely
avoid this impact 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, 1,540 m (5,052 ft) in
intermediate depths, and 2,140 m (7,020
ft) in shallow depths, when the 36airgun array is in use at 9 m (29.5 ft) tow
depth from the vessel to be exposed to
levels of sound believed to have a
minimal chance of causing permanent
threshold shift;
(4) The fact that cetaceans would have
to be closer than 1,100 m (3,609 ft) in
deep water, 1,810 m (5,938 ft) in
intermediate depths, and 2,520 m (8,268
ft) in shallow depths, when the 36airgun array is in use at 12 m (39.4 ft)
tow depth from the vessel to be exposed
to levels of sound believed to have a
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minimal chance of causing permanent
threshold shift;
(5) The fact that cetaceans would have
to be closer than 1,200 m (3,937 ft) in
deep water, 1,975 m (6,480 ft) in
intermediate depths, and 2,750 m (9,022
ft) in shallow depths, when the 36airgun array is in use at 15 m (49.2 ft)
tow depth from the vessel to be exposed
to levels of sound believed to have a
minimal chance of causing permanent
threshold shift;
(6) The fact that cetaceans would have
to be closer than 40 m (131 ft) in deep
water, 60 m (197 ft) in intermediate
depths, and 296 m (971 ft) in shallow
depths, when the single airgun is in use
at six to 15 m (20 to 49.2 ft) tow depth
from the vessel to be exposed to levels
of sound believed to have a minimal
chance of causing permanent threshold
shift;
(7) The fact that pinnipeds would
have to be closer than 400 m (1,312 ft)
in deep water, 550 m (1,804 ft) in
intermediate depths, and 680 m (2,231
ft) in shallow depths, when the 36airgun array is in use at 9 m (29.5 ft) tow
depth from the vessel to be exposed to
levels of sound believed to have a
minimal chance of causing permanent
threshold shift;
(8) The fact that pinnipeds would
have to be closer than 460 m (1,509 ft)
in deep water, 615 m (2,018 ft) in
intermediate depths, and 770 m (2,526
ft) in shallow depths, when the single
airgun is in use at 12 m (39.4 ft) tow
depth from the vessel to be exposed to
levels of sound believed to have a
minimal chance of causing permanent
threshold shift;
(9) The fact that pinnipeds would
have to be closer than 520 m (1,706 ft)
in deep water, 690 m (2,264 ft) in
intermediate depths, and 865 m (2,838
ft) in shallow depths, when the single
airgun is in use at 15 m (49.2 ft) tow
depth from the vessel to be exposed to
levels of sound believed to have a
minimal chance of causing permanent
threshold shift;
(10) The fact that pinnipeds would
have to be closer than 12 m (39.4 ft) in
deep water, 18 m (59 ft) in intermediate
depths, and 150 m (492 ft) in shallow
depths, when the single airgun is in use
at six to 15 m (20 to 49.2 ft) tow depth
from the vessel to be exposed to levels
of sound believed to have a minimal
chance of causing permanent threshold
shift; and
(11) The likelihood that marine
mammal detection ability by trained
visual observers is high at close
proximity to the vessel.
We do not anticipate that any injuries,
serious injuries, or mortalities would
occur as a result of the Observatory’s
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planned marine seismic surveys, and we
do not propose to authorize injury,
serious injury or mortality for this
survey. We anticipate only short-term
behavioral disturbance to occur during
the conduct of the survey activities.
Tables 5, 6, and 7 of this document
outline the number of requested Level B
harassment takes that we anticipate 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), we do not expect the activity to
impact rates of recruitment or survival
for any affected species or stock.
Further, the seismic surveys would not
take place in areas of significance for
marine mammal feeding, resting,
breeding, or calving and would 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 hour
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 we anticipate that the seismic
operations would occur on consecutive
days, the estimated duration of the Juan
de Fuca Plate survey would last no more
than 17 days, the Cascadia Thrust Zone
survey would last approximately three
days, and the Cascadia Subduction
Margin survey would occur over
10 days.
Because the Langseth will move
continuously along planned tracklines,
each seismic survey would increase
sound levels in the marine environment
surrounding the vessel for 21 days
during the first and second study and
for 10 days during the last study. There
will be an estimated 4-day period of
non-seismic activity between the second
and third survey.
Of the 31 marine mammal species
under our jurisdiction that are known to
occur or likely to occur in the study
area, six of these species and two stocks
are listed as endangered under the
Endangered Species Act: The blue, fin,
humpback, north Pacific right, sei, and
sperm whales; the southern resident
stock of killer whales; and the eastern
U.S. stock of the Steller sea lion. These
species are also categorized as depleted
under the Marine Mammal Protection
Act. With the exception of North Pacific
right whales, the Observatory has
requested authorized take for these
listed species. To protect these animals
(and other marine mammals in the
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study area), the Observatory must cease
or reduce airgun operations if animals
enter designated zones.
Based on available data, we do not
expect the Observatory to encounter five
of the 31 species under our jurisdiction
in the proposed survey areas. They
include the following: The north Pacific
right, false killer, and short-finned pilot
whales; the California sea lion; and the
bottlenose dolphin because of the
species’ rare and/or extralimital
occurrence in the survey areas. As
mentioned previously, we estimate that
26 species of marine mammals under
our jurisdiction could be potentially
affected by Level B harassment over the
course of the proposed authorization.
For each species, these numbers are
small, relative to the regional or overall
population size and we have provided
the regional population estimates for the
marine mammal species that may be
taken by Level B harassment in Tables
5, 6, and 7 in this document. Our
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]).
We have preliminarily determined,
provided that the aforementioned
mitigation and monitoring measures are
implemented, that the impact of
conducting three marine seismic
surveys off Oregon and Washington in
the northwestern Pacific Ocean, June
through July, 2012, may result, at worst,
in a temporary modification in behavior
and/or low-level physiological effects
(Level B harassment) of small numbers
of certain species of marine mammals.
See Tables 5, 6, and 7 for the requested
authorized take numbers of cetaceans.
While these species may make
behavioral modifications, including
temporarily vacating the area during the
operation of the airgun(s) to avoid the
resultant acoustic disturbance, the
availability of alternate areas within
these areas and the short duration of the
research activities, have led us to
preliminarily 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, we
preliminarily find that the Observatory’s
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planned research activities will result in
the incidental take of small numbers of
marine mammals, by Level B
harassment only, and that the required
measures mitigate impacts to affected
species or stocks of marine mammals to
the lowest level practicable.
Impact on Availability of Affected
Species or Stock for Taking for
Subsistence Uses
Section 101(a)(5)(D) of the Marine
Mammal Protection Act also requires us
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
(northeastern Pacific Ocean) that
implicate section 101(a)(5)(D) of the
Marine Mammal Protection Act.
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Endangered Species Act
Of the species of marine mammals
that may occur in the proposed survey
area, several are listed as endangered
under the Endangered Species Act,
including the blue, fin, humpback,
north Pacific right, sei, and sperm
whales. The Observatory did not request
take of endangered north Pacific right
whales because of the low likelihood of
encountering these species during the
cruise.
Under section 7 of the Act, the
Foundation has initiated formal
consultation with the Service’s, Office
of Protected Resources, Endangered
Species Act Interagency Cooperation
Division, on this proposed seismic
survey. We (i.e., National Marine
Fisheries Service, Office of Protected
Resources, Permits and Conservation
Division), have also initiated formal
consultation under section 7 of the Act
with the Endangered Species Act
Interagency Cooperation Division to
obtain a Biological Opinion (Opinion)
evaluating the effects of issuing an
incidental harassment authorization for
threatened and endangered marine
mammals and, if appropriate,
authorizing incidental take. We will
conclude the formal section 7
consultation prior to making a
determination on whether or not to
issue the authorization. If we issue the
take authorization, the Foundation and
the Observatory must comply with the
Terms and Conditions of the Opinion’s
Incidental Take Statement in addition to
the mitigation and monitoring
requirements included in the issued
take authorization.
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National Environmental Policy Act
(NEPA)
With its complete application, the
Foundation and the Observatory
provided an ‘‘Environmental
Assessment and Finding of No
Significant Impact Determination
Pursuant to the National Environmental
Policy Act, (NEPA: 42 U.S.C. 4321 et
seq.) and Executive Order 12114 for a
‘‘Marine Seismic Survey in the
northeastern Pacific Ocean, 2012,’’
which incorporates an ‘‘Environmental
Assessment of a Marine Geophysical
Survey by the R/V Marcus G. Langseth
in the northeastern Pacific Ocean, June–
July 2012,’’ prepared by LGL Limited
environmental research associates.
The Assessment analyzes the direct,
indirect, and cumulative environmental
impacts of the specified activities on
marine mammals including those listed
as threatened or endangered under the
Endangered Species Act. We have
conducted an independent review and
evaluation of the document for
sufficiency and compliance with the
Council of Environmental Quality and
NOAA Administrative Order 216–6
§ 5.09(d), Environmental Review
Procedures for Implementing the
National Environmental Policy Act, and
have preliminarily determined that
issuance of the incidental harassment
authorization is not likely to result in
significant impacts on the human
environment. Consequently, we plan to
adopt the Foundation’s Assessment and
intend to prepare a Finding of No
Significant Impact for the issuance of
the authorization.
Proposed Authorization
As a result of these preliminary
determinations, we propose to authorize
the take of marine mammals incidental
to the Observatory’s proposed marine
seismic surveys in the northeast Pacific
Ocean, provided the previously
mentioned mitigation, monitoring, and
reporting requirements are incorporated.
The duration of the incidental
harassment authorization would not
exceed one year from the date of its
issuance.
Information Solicited
We request interested persons to
submit comments and information
concerning this proposed project and
our preliminary determination of
issuing a take authorization (see
ADDRESSES). Concurrent with the
publication of this notice in the Federal
Register, we will forward copies of this
application to the Marine Mammal
Commission and its Committee of
Scientific Advisors.
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25991
Dated: April 27, 2012.
Helen M. Golde,
Acting Director, Office of Protected Resources,
National Marine Fisheries Service.
[FR Doc. 2012–10627 Filed 5–1–12; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF DEFENSE
Department of the Army
[Docket ID: USA–2012–0008]
Privacy Act of 1974; System of
Records
Defense Information Systems
Agency, DoD.
ACTION: Notice to Add a New System of
Records.
AGENCY:
The Department of the Army
proposes to add a new system of records
in its inventory of record systems
subject to the Privacy Act of 1974 (5
U.S.C. 552a), as amended.
DATES: This proposed action will be
effective on June 1, 2012 unless
comments are received which result in
a contrary determination.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
• Federal Rulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Federal Docket Management
System Office, 4800 Mark Center Drive,
East Tower, 2nd Floor, Suite 02G09,
Alexandria, VA 22350–3100.
Instructions: All submissions received
must include the agency name and
docket number for this Federal Register
document. The general policy for
comments and other submissions from
members of the public is to make these
submissions available for public
viewing on the Internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
FOR FURTHER INFORMATION CONTACT: Mr.
Leroy Jones, Jr., Department of the
Army, Privacy Office, U.S. Army
Records Management and
Declassification Agency, 7701 Telegraph
Road, Casey Building, Suite 144,
Alexandria, VA 22315–3827 or by
phone at 703–428–6185.
SUPPLEMENTARY INFORMATION: The
Department of the Army notices for
systems of records subject to the Privacy
Act of 1974 (5 U.S.C. 552a), as amended,
have been published in the Federal
Register and are available from the
address in FOR FURTHER INFORMATION
CONTACT. The proposed system report,
SUMMARY:
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Agencies
[Federal Register Volume 77, Number 85 (Wednesday, May 2, 2012)]
[Notices]
[Pages 25966-25991]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-10627]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XB105
Takes of Marine Mammals Incidental to Specified Activities; Three
Marine Geophysical Surveys in the Northeast Pacific Ocean, June Through
July 2012
AGENCY: National Marine Fisheries Service, National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental harassment authorization; request
for comments.
-----------------------------------------------------------------------
SUMMARY: We have received an application from the Lamont-Doherty Earth
Observatory, a part of Columbia University, for an Incidental
Harassment Authorization to take marine mammals, by harassment,
incidental to conducting three consecutive marine geophysical surveys
in the northeast Pacific Ocean, June through July 2012.
DATES: Comments and information must be received no later than May 31,
2012.
ADDRESSES: Comments on the application should be addressed to Tammy C.
Adams, Acting 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. We are 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 submitted comments are a part of the public record and we will
post 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.
To obtain an electronic copy of the application containing a list
of the references used in this document, write to the previously
mentioned address, telephone the contact listed here (see FOR FURTHER
INFORMATION CONTACT), or visit the Internet at: https://www.nmfs.noaa.gov/pr/permits/incidental.htm#applications.
The National Science Foundation's (Foundation) draft Environmental
Assessment (Assessment) pursuant to the National Environmental Policy
Act of 1969 and Executive Order 12114 is also available at the same
Internet address. The Assessment incorporates an ``Environmental
Assessment of a marine geophysical survey by the R/V Marcus G. Langseth
in the northeastern Pacific Ocean, June-July 2012,'' prepared by LGL
Limited environmental research associates, on behalf of the Foundation.
The public can view documents cited in this notice by appointment,
during regular business hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT: Jeannine Cody or Howard Goldstein,
National Marine Fisheries Service, Office of Protected Resources, (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: (1) We make certain findings; (2) the taking is
limited to harassment; and (3) we provide a notice of a proposed
authorization to the public for review.
We shall grant authorization for the incidental taking of small
numbers of marine mammals if we find 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. We have 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 Marine Mammal Protection Act
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 Act
establishes a 45-day time limit for our 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, we
must either issue or deny the authorization and must publish a notice
in the Federal Register within 30 days of our determination to issue or
deny the authorization.
Except with respect to certain activities not pertinent here, the
Marine Mammal Protection Act 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
We received an application on January 27, 2012, from the Lamont-
Doherty Earth Observatory (Observatory) for the taking by harassment,
of small numbers of marine mammals, incidental to conducting three
separate marine geophysical surveys in the northeast Pacific Ocean. We
determined the application complete and adequate on March 27, 2012.
The Observatory, with research funding from the U.S. National
Science Foundation (Foundation), plans to conduct three research
studies on the Juan de Fuca Plate, the Cascadia thrust zone, and the
Cascadia subduction margin in waters off the Oregon and Washington
coasts. The Observatory has proposed to conduct the first survey from
June 11 through July 5, 2012, the second survey from July 5 through
July 8, 2012, and the third survey from July 12 through July 23, 2012.
The Observatory plans to use one source vessel, the R/V Marcus G.
Langseth (Langseth), a seismic airgun array, a single hydrophone
streamer, and ocean bottom seismometers to conduct the geophysical
surveys.
[[Page 25967]]
The proposed surveys will provide data necessary to:
Characterize the evolution and state of hydration of the
Juan de Fuca plate at the Cascadia subduction zone;
Provide information on the buried structures in the
region; and
Assess the location, physical state, fluid budget, and
methane systems of the Juan de Fuca plate boundary and overlying crust.
The results of the three studies would provide background
information for generating improved earthquake hazards analyses and a
better understanding of the processes that control megathrust
earthquakes which are produced by a sudden slip along the boundary
between a subducting and an overriding plate.
In addition to the operations of the seismic airgun array and
hydrophone streamer, and the ocean bottom seismometers (seismometers),
the Observatory intends to operate a multibeam echosounder and a sub-
bottom profiler continuously throughout the surveys.
Acoustic stimuli (i.e., increased underwater sound) generated
during the operation of the seismic airgun arrays, 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 the Observatory has
requested an authorization to take 26 species of marine mammals by
Level B harassment. We do not expect that the use of the multibeam
echosounder, the sub-bottom profiler, or the ocean bottom seismometer
will result in the take of marine mammals and will discuss our
reasoning later in this notice. Also, we do not expect take to result
from a collision with the Langseth because it is a single vessel moving
at relatively slow speeds (4.6 knots (kts); 8.5 kilometers per hour
(km/h); 5.3 miles 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 Activities
Juan de Fuca Plate Survey
The first proposed seismic survey would begin on June 11, 2012, and
end on July 5, 2012. The Langseth would depart from Astoria, Oregon on
June 11, 2012, and transit to the survey area in the northeast Pacific
Ocean in international waters and the Exclusive Economic Zones of the
United States and Canada. The study area will encompass an area bounded
by approximately 43-48 degrees ([deg]) North by approximately 124-
130[deg] East (see Figure 1 in the Observatory's Application
1). Water depths in the survey area range from approximately
50 to 3,000 meters (m) (164 feet (ft) to 1.9 miles (mi)). At the
conclusion of the first survey, the Langseth would begin a second
three-day seismic survey on July 5, 2012, in the same area.
Typically, two-dimensional surveys such as this one, acquire data
along single track lines with wide intervals; cover large areas;
provide a coarse sampled subsurface image; and project less acoustic
energy into the environment than other types of seismic surveys. During
this survey, the Langseth would deploy a 36-airgun array as an energy
source, an 8-kilometer (km)-long (4.9 mi-long) hydrophone streamer, and
46 seismometers. The seismometers are portable, self-contained passive
receiver systems designed to sit on the seafloor and record seismic
signals generated primarily by airguns and earthquakes. As the Langseth
tows the airgun array along the survey lines, the hydrophone streamer
receives the returning acoustic signals and transfers the data to the
vessel's on-board processing system. The seismometers also record and
store the returning signals for later analysis.
The Observatory plans to discharge the airgun array along three
long transect lines and three semi-circular arcs using the seismometers
as the receivers and then repeat along the long transect lines in
multichannel seismic mode using the 8-km streamer as the receiver (see
Figure 1 in the Observatory's Application 1). Also, the
Observatory will use one support vessel, the R/V Oceanus (Oceanus) to
deploy 46 seismometers on the northern onshore-offshore line, retrieve
the 46 seismometers from the northern line, and then deploy 39
seismometers on the southern onshore-offshore lines and retrieve them
at the conclusion of the survey.
The first study (e.g., equipment testing, startup, line changes,
repeat coverage of any areas, and equipment recovery) will require
approximately 17 days to complete approximately 3,051 km (1,895.8 mi)
of transect lines. The total survey effort including contingency will
consist of approximately 2,878 km (1,788.3) of transect lines in depths
greater than 1,000 m (621.3 mi), 102 km (63.4 mi) in depths 100 to
1,000 m (328 to 3,280 ft), and 71 km (44.1 mi) in water depths less
than 100 m (328 ft). The northern and southern onshore-offshore lines
are 70 to 310 km (43.4 to 192.6 mi) and 15 to 450 km (9.3 to 279.6 mi)
from shore, respectively.
Data acquisition will include approximately 408 hours of airgun
operations (i.e., 17 days over 24 hours). The Observatory, the
Langseth's operator, will conduct all planned seismic activities, with
on-board assistance by the scientists who have proposed the study. The
Principal Investigators for the survey are Drs. S. Carbotte and H.
Carton (Lamont Doherty Earth Observatory, New York) and P. Canales
(Woods Hole Oceanographic Institution, Massachusetts). The vessel is
self-contained and the crew will live aboard the vessel for the entire
cruise.
Cascadia Thrust Zone Survey
The second proposed survey would begin on July 5, 2012, and end on
July 8, 2012. The survey would take place in the U.S. Exclusive
Economic Zone in waters off of the Oregon and Washington coasts. The
study area will encompass an area bounded by approximately 43.5-47[deg]
North by approximately 124-125[deg] East (see Figure 1 in the
Observatory's Application 2). Water depths in the survey area
range from approximately 50 to 1,000 m (164 ft to 0.62 mi). At the
conclusion of this survey, the Langseth would return to Astoria, Oregon
on July 8, 2012.
The Langseth would deploy a 36-airgun array as an energy source, 12
seismometers, and 48 seismometers (33 in Oregon and 15 in Washington)
onshore (on land). As stated previously, as the Langseth tows the
airgun array along the survey lines, the seismometers record the
returning acoustic signals for later analysis. The Observatory proposes
to use the Oceanus to deploy and retrieve the seismometers.
The Observatory plans to discharge the airgun array along a grid of
lines off Oregon and along an onshore-offshore line off Washington (see
Figure 1 in the Observatory's Application 2).
The proposed study (e.g., equipment testing, startup, line changes,
repeat coverage of any areas, and equipment recovery) will require
approximately 3 days to complete approximately 793 km (492.7 mi) of
transect lines. The total survey effort including contingency will
consist of approximately 5 km (3.1 mi) of transect lines in depths
greater than 1,000 m (621.3 mi), 501 km (311.3 mi) in depths 100 to
1,000 m (328 to 3,280 ft), and 287 km (178.3 mi) in water depths less
than 100 m (328 ft). The northern and southern legs of the onshore-
offshore lines are 15 to 70 km (9.3 to 43.5 mi) and 15 to 50 km (9.3 to
31.1 mi) from shore, respectively.
Data acquisition will include approximately 72 hours of airgun
operations (i.e., 3 days over 24 hours). The Principal Investigators
for the
[[Page 25968]]
second survey are Drs. A.M Trehu (Oregon State University) and G. Abers
and H. Carton (Lamont Doherty Earth Observatory, New York). The vessel
is self-contained and the crew will live aboard the vessel for the
entire cruise.
Cascadia Subduction Margin Survey
The last seismic survey would begin on July 12, 2012, and end on
July 23, 2012. The Langseth would depart from Astoria, Oregon on July
12, 2012, and transit to waters off of the Washington coast. The study
area encompasses an area bounded by approximately 46.5-47.5[deg] North
by approximately 124.5-126[deg] East (see Figure 1 in the Observatory's
Application 3). Water depths in the survey area range from
approximately 95 to 2,650 m (311.7 ft to 1.6 mi). At the conclusion of
this survey, the Langseth would return to Astoria, Oregon on July 23,
2012.
The Langseth would deploy a 36-airgun array as an energy source and
an 8-km-long (4.9 mi-long) hydrophone streamer. The Observatory plans
to discharge the airgun array along nine parallel lines that are spaced
eight km apart. If time permits, the Langseth would survey an
additional two lines perpendicular to the parallel lines (see Figure 1
in the Observatory's Application 3).
The proposed study (e.g., equipment testing, startup, line changes,
repeat coverage of any areas, and equipment recovery) will require
approximately 10 days to complete approximately 1,147 km (712.7 mi) of
transect lines. The total survey effort including contingency will
consist of approximately 785 km (487.8 mi) of transect lines in depths
greater than1,000 m (621.3 mi), 350 km (217.5 mi) of transect lines in
depths 100 to 1,000 m (328 to 3,280 ft), and 12 km (7.5 mi) of transect
lines in water depths less than 100 m (328 ft). The survey area is 32
to 150 km (19.9 to 93.2 mi) from shore.
Data acquisition will include approximately 240 hours of airgun
operations (i.e., 10 days over 24 hours). The Principal Investigators
for the third survey are Drs. W.S. Holbrook (University of Wyoming),
A.M. Trehu (Oregon State University), H.P. Johnson (University of
Washington), G.M. Kent (University of Nevada), and K. Keranen
(University of Oklahoma). The vessel is self-contained and the crew
will live aboard the vessel for the entire cruise.
Vessel Specifications
The Langseth, owned by the Foundation, is a seismic research vessel
with a quiet propulsion system that avoids interference with the
seismic signals emanating from the airgun array. The vessel is 71.5 m
(235 ft) long; has 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. It's two 3,550 horsepower
(hp) Bergen BRG-6 diesel engines 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 operational 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 during the first and last surveys, 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 (observer) will watch for marine mammals
before and during the proposed airgun operations. When stationed on the
observation platform, the observer's eye level will be approximately
21.5 m (71 ft) above sea level providing the observer an unobstructed
view around the entire vessel.
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, we propose to issue an
authorization to the Observatory that would be effective from June 9,
2012, to August 27, 2012.
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, 12, or 15
m (29.5, 39.4, or 49.2 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 Langseth's crew will space the first and last airguns 16 m
(52 ft) apart from one another. Of the 10 airguns, nine will fire
simultaneously while the tenth airgun will serve as a spare. The crew
will turn on the spare airgun in case one of the other airguns fail.
The Langseth will distribute the array across an area of approximately
24 by 16 m (78.7 by 52.5 ft) and will tow the array approximately 100 m
(328 ft) behind the vessel.
Juan de Fuca Plate Survey: This survey's array tow depth will be 9
m (29.5 ft) for the multichannel seismic survey using the hydrophone
streamer and 12 m (39.4 ft) during the survey using the seismometers.
During the multichannel seismic survey, each airgun array will emit a
pulse at approximately 16-second (s) intervals which corresponds to a
shot interval of approximately 37.5 m (123 ft). During the survey using
the seismometers, each airgun array will emit a pulse at approximately
200-s intervals which corresponds to a shot interval of approximately
500 m (1,640.4 ft). During firing, the airguns will emit a brief
(approximately 0.1 s) pulse of sound; during the intervening periods of
operations, the airguns are silent.
Cascadia Thrust Zone Survey: The survey's array tow depth will be
12 m (39.4 ft). During this survey, each airgun array will emit a pulse
at approximately 40-s intervals which corresponds to a shot interval of
approximately 100 m (328 ft). During firing, the airguns will emit a
brief (approximately 0.1 s) pulse of sound; during the intervening
periods of operations, the airguns are silent.
Cascadia Subduction Margin Survey: The survey's array tow depth
will be 15 m (49.2 ft). During this survey, each airgun array will emit
a pulse at approximately 20-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 are 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 ([micro]Pa), where 1 pascal (Pa) is
the pressure resulting from a force of one newton exerted over an area
of one square meter. In this document, we express sound pressure level
as the ratio of a measured sound pressure and a reference level. The
commonly used reference pressure level in underwater acoustics is 1
FPa, and the units for sound pressure levels are dB re: 1 [mu]Pa.
Sound pressure level (in decibels (dB)) = 20 log (pressure/reference
pressure)
[[Page 25969]]
Sound pressure level is an instantaneous measurement and can be
expressed as the peak, the peak-peak (p-p), or the root mean square.
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 sound pressure level in this document refer to the root mean square
unless otherwise noted. Sound pressure level 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 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 the
Observatory on the Langseth is 236 to 265 dB re: 1
[mu]Pa(p-p) and the root mean square 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 root mean square 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, the Observatory 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. Appendix A of the Foundation's Environmental Assessment
provides a detailed description of the modeling for marine seismic
source arrays for species mitigation and Appendix B(3) of the
Assessment discusses the characteristics of the airgun pulses. These
are the 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. Refer to the authorization application and
Assessment 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.
The Observatory used the results from the Gulf of Mexico study to
determine the algorithm for its model that calculates the exclusion
zones for the 36-airgun array and the single airgun. These values
designate mitigation zones and the Observatory uses them to estimate
take (described in greater detail in Section VII of the application and
Section IV of the Foundation's Environmental Assessment) for marine
mammals.
Comparison of the Tolstoy et al. (2009) calibration study with the
Observatory's model for the Langseth's 36-airgun array indicated that
the model represents the actual received levels, within the first few
kilometers and the locations of the predicted exclusions zones.
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 depths in the proposed surveys (9, 12, or 15
m; 29.5, 39.4, or 49.2 ft), the Observatory used the following
correction factors for estimating the received levels during the
proposed surveys (see Table 1). The correction factors are 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, 12, or 15 m
(29.5, 39.4, or 49.2 ft) (LGL, 2008).
Table 1--Correction Factors for Estimating the Received Levels for Three
Proposed Surveys in the Northeast Pacific Ocean, during June-July 2012
------------------------------------------------------------------------
Array tow depth 160-dB 180-dB 190-dB
------------------------------------------------------------------------
9............................................ 1.285 1.338 1.364
12........................................... 1.467 1.577 1.545
15........................................... 1.647 1.718 1.727
------------------------------------------------------------------------
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 exclusion zones are essentially
the same at different tow depths. The Observatory's model does not
allow for bottom interactions, and thus is most directly applicable to
deep water.
Table 2 summarizes the predicted distances at which one would
expect to receive three sound levels (160-, 180-, and 190-dB) from the
36-airgun array and a single airgun. To avoid the potential for injury
or permanent physiological damage (Level A harassment), we (NMFS, 1995,
2000), we have concluded that cetaceans and pinnipeds should not be
exposed to pulsed underwater noise at received levels exceeding 180 dB
re: 1 [mu]Pa and 190 dB re: 1 [mu]Pa, respectively. The 180-dB and 190-
dB level shutdown criteria are applicable to cetaceans and pinnipeds,
respectively, specified by us (NMFS, 1995, 2000). The Observatory used
these levels to establish the exclusion zones. We also assume that
marine mammals exposed to levels exceeding 160 dB re: 1 [micro]Pa may
experience Level B harassment.
Table 2--Measured (Array) or Predicted (Single Airgun) Distances to Which Sound Levels Greater Than or Equal to
160, 180, and 190 dB re: 1 [mu]Pa That Could Be Received During the Three Proposed Surveys in the Northeast
Pacific Ocean, During June-July 2012
----------------------------------------------------------------------------------------------------------------
Predicted RMS distances \2\ (m)
Source and volume (in\3\) Tow depth Water depth (m) --------------------------------
(m) 160 dB 180 dB 190 dB
----------------------------------------------------------------------------------------------------------------
Single Bolt airgun (40 in\3\)......... \1\ 6-15 >1,000.................... 385 40 12
100 to 1,000.............. 578 60 18
<100...................... 1,050 296 150
36-Airgun Array (6,600 in\3\)......... 9 >1,000.................... 3,850 940 400
100 to 1,000.............. 12,200 1,540 550
<100...................... 20,550 2,140 680
[[Page 25970]]
36-Airgun Array (6,600 in\3\)......... 12 >1,000.................... 4,400 1,100 460
100 to 1,000.............. 13,935 1,810 615
<100...................... 23,470 2,250 770
36-Airgun Array (6,600 in\3\)......... 15 >1,000.................... 4,490 1,200 520
100 to 1,000.............. 15,650 1,975 690
<100...................... 26,350 2,750 865
----------------------------------------------------------------------------------------------------------------
\1\ 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 exclusion zones are essentially the same at
different tow depths.
\2\ The Observatory has based the radii for the array on data in Tolstoy et al. (2009) and has corrected for tow
depth using modeled results. They have based the predicted radii for a single airgun upon their model (see
Figure 3 in application 1).
Ocean Bottom Seismometers
The Observatory proposes to use the Woods Hole Oceanographic
Institution ``D2'' seismometer during the cruise. The seismometer is
approximately one meter in height and has a maximum diameter of 50
centimeters (cm). The anchor (2.5 x 30.5 x 38.1 cm) is hot-rolled steel
and weighs 23 kilograms. The acoustic release transponder, located on
the vessel, communicates with the seismometer at a frequency of 9 to 11
kilohertz (kHz). The source level of the release signal is 190 dB re: 1
[mu]Pa. The received signal activates the seismometer's burn-wire
release assembly which then releases the seismometer from the anchor.
The seismometer then floats to the ocean surface for retrieval by the
Oceanus.
Multibeam Echosounder
The Langseth will operate a Kongsberg EM 122 multibeam echosounder
concurrently during airgun operations to map characteristics of the
ocean floor. The hull-mounted echosounder emits brief pulses of sound
(also called a ping) (10.5 to 13 kHz) in a fan-shaped beam that extends
downward and to the sides of the ship. The transmitting beamwidth is 1
or 2[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 2 to 15 ms long in water depths up
to 2,600 m (8,530 ft). The echosounder uses frequency-modulated chirp
pulses up to 100-ms long in water greater than 2,600 m (8,530 ft). The
successive transmissions span an overall cross-track angular extent of
about 150[deg], with 2-ms gaps between the pulses for successive
sectors.
Sub-Bottom Profiler
The Langseth will also operate a Knudsen Chirp 3260 sub-bottom
profiler concurrently during airgun and echosounder operations to
provide information about the sedimentary features and bottom
topography. The profiler is capable of reaching depths of 10,000 m (6.2
mi). The dominant frequency component is 3.5 kHz and a hull-mounted
transducer on the vessel directs the beam downward in a 27[deg] cone.
The power output is 10 kilowatts (kW), but the actual maximum radiated
power is three kilowatts 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.
We expect 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. We also expect 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.
We do 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-one marine mammal species under our jurisdiction may occur
in the proposed survey areas, including 19 odontocetes (toothed
cetaceans), seven mysticetes (baleen whales), and five species of
pinniped during June through July, 2012. Six of these species and two
stocks 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; the
southern resident stock of killer (Orcinus orca) whales; and the
eastern U.S. stock of the Steller sea lion (Eumetopias jubatus).
The U.S. Fish and Wildlife Service manages the northern sea otter
(Enhydra lutis) (listed under the Endangered Species Act). Because this
species is not under our jurisdiction, we do not consider this species
further in this notice.
Based on available data, the Observatory does not expect to
encounter five of the 31 species in the proposed survey areas. They
include the: the north Pacific right, false killer (Pseudorca
crassidens), and short-finned pilot (Globicephala macrorhynchus)
whales; the California sea lion (Zalophus californianus); and the
bottlenose dolphin (Tursiops truncatus) because of these species' rare
and/or extralimital occurrence in the survey areas. Accordingly, we did
not consider these species in greater detail and the proposed
authorization will only address requested take authorizations for 26
species: Six mysticetes, 16 odontocetes, and four species of pinniped.
Of these 26 species, the most common marine mammals in the survey
area would be the: harbor porpoise (Phocoena phocoena), Dall's porpoise
(Phocoenoides dalli), northern fur seal (Callorhinus ursinus), and
northern elephant seal (Mirounga angustirostris).
[[Page 25971]]
Table 3 presents information on the abundance, distribution, and
conservation status of the marine mammals that may occur in the
proposed survey area June through July 2012.
Table 3--Habitat, Abundance, Density, and ESA Status of Marine Mammals That May Occur in or Near the Proposed
Seismic Survey Areas in the Northeast Pacific Ocean
[See text and Tables 2 and 3 in the Observatory's applications and the Foundation's Environmental Assessment for
further details.]
----------------------------------------------------------------------------------------------------------------
Density \3\
Species Occurrence in Habitat Abundance in the ESA \2\ /
area NW Pacific \1\ 1,000 km \2\
----------------------------------------------------------------------------------------------------------------
Mysticetes
North Pacific right whale.... Rare............ Coastal, shelf, \4\ 31 EN 0
offshore.
Gray whale................... Common *........ Coastal, shallow \5\ 19,126 DL 3.21
shelf.
Humpback whale............... Common *........ Mainly nearshore \6\ 20,800 EN 0.81
and banks.
Minke whale.................. Rare............ Nearshore, \7\ 9,000 NL 0.46
offshore.
Sei whale.................... Rare............ Mostly pelagic.. \8\ 12,620 EN 0.16
Fin whale.................... Common.......... Slope, pelagic.. \9\ 13,620- EN 1.29
18,680
Blue whale................... Rare............ Pelagic and 2,497 EN 0.18
coastal.
Odontocetes
Sperm whale.................. Common.......... Pelagic, steep \10\ 24,000 EN 1.02
topography.
Pygmy sperm whale............ Rare............ Deep, off shelf. N.A. NL 0.71
Dwarf sperm whale............ Rare............ Deep, shelf, N.A. NL 0.71
slope.
Cuvier's beaked whale........ Common.......... Pelagic......... 2,143 NL 0.43
Baird's beaked whale......... Common.......... Pelagic......... 907 NL 1.18
Blainville's beaked whale.... Rare............ Pelagic......... \11\ 1,024 NL 1.75
Hubb's beaked whale.......... Rare............ Slope, offshore. \11\ 1,024 NL 1.75
Stejneger's beaked whale..... Common.......... Slope, offshore. \11\ 1,024 NL 1.75
Common bottlenose dolphin.... Rare............ Coastal, shelf, \12\ 1,006 NL 0
deep.
Striped dolphin.............. Rare............ Off continental 10,908 NL 0.04
shelf.
Short-beaked common dolphin.. Common.......... Shelf, pelagic, 411,211 NL 10.28
mounts.
Pacific white-sided dolphin.. Abundant........ Offshore, slope. 26,930 NL 34.91
Northern right whale dolphin. Common.......... Slope, offshore 8,334 NL 12.88
waters.
Risso's dolphin.............. Common.......... Shelf, slope, 6,272 NL 11.19
mounts.
False killer whale........... Rare............ Pelagic......... N.A. NL 0
Killer whale................. Common.......... Widely 2,250-2,700 NL/EN \13\ 1.66
distributed.
Short-finned pilot whale..... Rare............ Pelagic, high- 760 NL 0
relief.
Harbor porpoise.............. Abundant........ Coastal and \13\ 55,255 NL 632.4
inland waters.
Dall's porpoise.............. Abundant........ Shelf, slope, 42,000 NL 83.82
offshore.
Pinnipeds
Northern fur seal............ Common.......... Pelagic, \5\ 653,171 NL 83.62
offshore.
California sea lion.......... Rare............ Coastal, shelf.. 296,750 NL 0
Steller sea lion............. Common *........ Coastal, shelf.. \5\ 58,334- T 13.12
72,223
Harbor seal.................. Abundant *...... Coastal......... \14\ 24,732 NL 292.3
Northern elephant seal....... Common.......... Coastal, pelagic \15\ 124,000 NL 45.81
in migration.
----------------------------------------------------------------------------------------------------------------
N.A.--Data not available or species status was not assessed.
* In nearshore survey areas, rare elsewhere.
\1\ Abundance given for the California/Oregon/Washington or Eastern North Pacific stock (Carretta et al.
2011a,b), unless otherwise stated.
\2\ Endangered Species Act: EN = Endangered, T = Threatened, DL = Delisted, NL = Not listed.
\3\ Density estimate as listed in Table 3 of the Observatory's applications. Refer to pg. 48 of application
1, pg. 47 of application 2, and pg. 47 of application 3 for specific references.
\4\ Bering Sea (Wade et al. 2010).
\5\ Eastern North Pacific (Allen and Angliss 2011).
\6\ North Pacific (Barlow et al. 2009).
\7\ North Pacific (Wada 1976).
\8\ North Pacific (Tillman 1977).
\9\ North Pacific (Ohsumi and Wada 1974).
\10\ Eastern Temperate North Pacific (Whitehead 2002a).
\11\ All mesoplodont whales.
\12\ Offshore stock (Carretta et al. 2011a).
\13\ The Eastern North Pacific Southern Resident Stock of killer whales is listed as Endangered under the ESA.
\14\ Northern Oregon/Washington Coast and Northern California/Southern Oregon stocks.
\15\ Oregon/Washington Coastal Stock (Carretta et al. 2011a).
Refer to Sections III and IV of the Observatory's applications 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 applications also
present how the Observatory calculated the estimated densities for the
marine mammals in the proposed survey area. We have reviewed these data
and determined them to be the best available scientific information for
the purposes of the proposed incidental harassment authorization.
[[Page 25972]]
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 is not
an injury (Southall et al., 2007). Although we cannot exclude the
possibility entirely, 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 in this document, we expect
some behavioral disturbance, but we expect the disturbance to be
localized.
Tolerance
Studies on marine mammals' tolerance to sound in the natural
environment are relatively rare. Richardson et al. (1995) defined
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 the Environmental Assessment). 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).
We expect that the masking effects of pulsed sounds (even from
large arrays of airguns) on marine mammal calls and other natural
sounds will be limited, although there are very few specific data on
this. Because of the intermittent nature and low duty cycle of seismic
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. We understand that some baleen and toothed whales continue
calling in the presence of seismic pulses, and that some researchers
have heard these calls 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 have 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). Several studies have reported hearing dolphins and
porpoises calling while airguns were 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, we expect that the masking effects of seismic pulses
will be minor, given the normally intermittent nature of seismic
pulses. Refer to Appendix B(4) of the Foundation's Assessment 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. There are less detailed data
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
[[Page 25973]]
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 Foundation's Assessment, 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 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 (2.5 to 9.3 mi)
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 the Foundation's Assessment 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 [mu]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 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 the
Foundation's Assessment). 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).
A few studies have documented reactions of migrating and feeding
(but not wintering) gray whales to seismic surveys. 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) root
mean square basis, and that 10 percent of feeding whales interrupted
feeding at received levels of 163 dB re: 1 [mu]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).
Occasionally, observers have seen various species of Balaenoptera
(blue, sei, fin, and minke whales) in areas ensonified by airgun pulses
(Stone, 2003; MacLean and Haley, 2004; Stone and Tasker, 2006), and
have localized calls from blue and fin whales 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
[[Page 25974]]
(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. We do not know 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 appear 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 Angliss, 2011).
Toothed Whales--There is little systematic information available
about reactions of toothed whales to noise pulses. There are few
studies on toothed whales similar to the more extensive baleen whale/
seismic pulse work summarized earlier in Appendix B of the Foundation's
Assessment. 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 (observers) 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
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,
observers 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 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 the Foundation's Assessment 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
[[Page 25975]]
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
underway within the vicinity of the animals (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 the
Foundation's Assessment).
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)(3) of the
Foundation's Assessment. 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 (Southall et al., 2007).
Researchers have studied temporary threshold shift in certain
captive odontocetes and pinnipeds exposed to strong sounds (reviewed in
Southall et al., 2007). However, there has been no specific
documentation of temporary threshold shift let alone permanent hearing
damage, i.e., permanent threshold shift, in free-ranging marine mammals
exposed to sequences of airgun pulses during realistic field
conditions.
Temporary Threshold Shift--This is the mildest form of hearing
impairment that can occur during exposure to a strong sound (Kryter,
1985). While experiencing temporary threshold shift, the hearing
threshold rises and a sound must be stronger in order to be heard. At
least in terrestrial mammals, temporary threshold shift can last from
minutes or hours to (in cases of strong shifts) days. For sound
exposures at or somewhat above the temporary threshold shift threshold,
hearing sensitivity in both terrestrial and marine mammals recovers
rapidly after exposure to the noise ends. There are few data on sound
levels and durations necessary to elicit mild temporary threshold shift
for marine mammals, and none of the published data focus on temporary
threshold shift elicited by exposure to multiple pulses of sound.
Southall et al. (2007) summarizes available data on temporary threshold
shift in marine mammals. Table 2 (introduced earlier in this document)
presents the estimated distances from the Langseth's airguns at which
the received energy level (per pulse, flat-weighted) would be greater
than or equal to 180 or 190 dB re: 1 [micro]Pa.
Researchers have derived temporary threshold shift 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 temporary threshold shift was lower (Lucke et al.,
2009). If these results from a single animal are representative, it is
inappropriate to assume that onset of temporary threshold shift occurs
at similar received levels in all odontocetes (cf. Southall et al.,
2007). Some cetaceans apparently can incur temporary threshold shift at
considerably lower sound exposures than are necessary to elicit
temporary threshold shift 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 temporary threshold
shift. 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 temporary threshold shift onset may also be higher in
baleen whales (Southall et al., 2007). For this proposed study, the
Observatory expects no cases of temporary threshold shift 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 temporary threshold shift to occur.
In pinnipeds, researchers have not measured temporary threshold
shift thresholds associated with exposure to brief pulses (single or
multiple) of underwater sound. Initial evidence from more prolonged
(non-pulse) exposures suggested that some pinnipeds (harbor seals in
particular) incur temporary threshold shift 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
temporary threshold shift threshold for pulsed sounds would be
approximately 181 to 186 dB re: 1 [mu]Pa
[[Page 25976]]
(Southall et al., 2007), or a series of pulses for which the highest
sound exposure level values are a few decibels lower. Corresponding
values for California sea lions and northern elephant seals are likely
to be higher (Kastak et al., 2005).
Permanent Threshold Shift--When permanent threshold shift 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 permanent threshold shift 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 temporary threshold shift, there has been further speculation
about the possibility that some individuals occurring very close to
airguns might incur permanent threshold shift (e.g., Richardson et al.,
1995, p. 372ff; Gedamke et al., 2008). Single or occasional occurrences
of mild temporary threshold shift are not indicative of permanent
auditory damage, but repeated or (in some cases) single exposures to a
level well above that causing temporary threshold shift onset might
elicit permanent threshold shift.
Relationships between temporary threshold shift and permanent
threshold shift thresholds have not been studied in marine mammals, but
are assumed to be similar to those in humans and other terrestrial
mammals. Permanent threshold shift might occur at a received sound
level at least several decibels above that inducing mild temporary
threshold shift if the animal were exposed to strong sound pulses with
rapid rise times--see Appendix B(6) of the Foundation's Assessment.
Based on data from terrestrial mammals, a precautionary assumption is
that the permanent threshold shift threshold for impulse sounds (such
as airgun pulses as received close to the source) is at least six
decibels higher than the temporary threshold shift threshold on a peak-
pressure basis, and probably greater than six decibels (Southall et
al., 2007).
Given the higher level of sound necessary to cause permanent
threshold shift as compared with temporary threshold shift, it is
considerably less likely that permanent threshold shift would occur.
Baleen whales generally avoid the immediate area around operating
seismic vessels, as do some other marine mammals.
Stranding and Mortality
When a living 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''.
Marine mammals are known to strand for a variety of reasons, such
as infectious agents, biotoxicosis, starvation, fishery interaction,
ship strike, unusual oceanographic or weather events, sound exposure,
or combinations of these stressors sustained concurrently or in series.
However, the cause or causes of most strandings are unknown (Geraci et
al., 1976; Eaton, 1979; Odell et al., 1980; Best, 1982). Numerous
studies suggest that the physiology, behavior, habitat relationships,
age, or condition of cetaceans may cause them to strand or might pre-
dispose them to strand when exposed to another phenomenon. These
suggestions are consistent with the conclusions of numerous other
studies that have demonstrated that combinations of dissimilar
stressors commonly combine to kill an animal or dramatically reduce its
fitness, even though one exposure without the other does not produce
the same result (Chroussos, 2000; Creel, 2005; DeVries et al., 2003;
Fair and Becker, 2000; Foley et al., 2001; Moberg, 2000; Relyea, 2005a;
2005b; Romero, 2004; Sih et al., 2004).
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 mid-frequency active sonar and most involved
beaked whales.
Over the past 12 years, there have been five stranding events
coincident with military mid-frequency active sonar use in which
exposure to sonar is believed to have been a contributing factor to
strandings: Greece (1996); the Bahamas (2000); Madeira (2000); Canary
Islands (2002); and Spain (2006). Refer 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 Observatory's 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 the Foundation's Assessment 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;
(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
acoustically-mediated 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 deep-
diving cetaceans exposed to sonar. However, the evidence for this
remains circumstantial and associated with exposure to naval mid-
frequency sonar,
[[Page 25977]]
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;
Fern[aacute]ndez 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,
two Cuvier's beaked whales stranded in the Gulf of California, Mexico
while the Observatory's R/V Maurice Ewing had been operating a 20-
airgun (8,490 in\3\) 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). We anticipate no injuries of beaked whales
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 the
Observatory 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 noise-induced bubble
formations (Crum et al., 2005) are implausible in the case of exposure
to an impulsive broadband source like an airgun array. If seismic
surveys disrupt diving patterns of deep-diving species, this might
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 non-
auditory effects can be expected (Southall et al., 2007), or any
meaningful quantitative predictions of the numbers (if any) of marine
mammals that might be affected in those ways. Marine mammals that show
behavioral avoidance of seismic vessels, including most baleen whales
and some odontocetes, are especially unlikely to incur non-auditory
physical effects.
Potential Effects of Other Acoustic Devices
Multibeam Echosounder
The Observatory will operate the Kongsberg EM 122 multibeam
echosounder from the source vessel during the planned study. Sounds
from the multibeam echosounder 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 echosounder is at
frequencies near 12 kHz, and the maximum source level is 242 dB re: 1
[mu]Pa. The beam is narrow (1 to 2[deg]) in fore-aft extent and wide
(150[deg]) 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 15-ms
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 echosounder 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 temporary threshold
shift.
Navy sonars 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 echosounder. The area of possible influence of the
echosounder 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 the Observatory'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
the animal. The following section outlines possible effects of an
echosounder on marine mammals.
Masking--Marine mammal communications will not be masked
appreciably by the echosounder's 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 echosounder's 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
[[Page 25978]]
no dispersal by pilot whales (Globicephala melas) (Rendell and Gordon,
1999), and the previously-mentioned beachings by beaked whales. During
exposure to a 21 to 25 kHz ``whale-finding'' sonar with a source level
of 215 dB re: 1 [micro]Pa, 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 Observatory's echosounder, 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 echosounder.
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 echosounder
proposed for use by the Observatory is quite different than sonar used
for navy operations. The echosounder's pulse duration is very short
relative to the naval sonar. Also, at any given location, an individual
marine mammal would be in the echosounder's beam for much less time
given the generally downward orientation of the beam and its narrow
fore-aft beamwidth; navy sonar often uses near-horizontally-directed
sound. Those factors would all reduce the sound energy received from
the echosounder relative to that from naval sonar.
Based upon the best available science, we believe that the brief
exposure of marine mammals to one pulse, or small numbers of signals,
from the echosounder is not likely to result in the harassment of
marine mammals.
Sub-Bottom Profiler
The Observatory will also operate a sub-bottom profiler from the
source vessel during the proposed survey. The profiler's sounds are
very short pulses, occurring for one to four ms once every second. Most
of the energy in the sound pulses emitted by the profiler 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 [micro]Pa.
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 a profiler 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 temporary threshold shift.
Masking--Marine mammal communications will not be masked
appreciably by the profiler's 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
profiler's 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 profiler
are likely to be similar to those for other pulsed sources if received
at the same levels. However, the pulsed signals from the profiler are
considerably weaker than those from the echosounder. 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 profiler 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 profiler operates
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 mammals would be close enough
for there to be any possibility of effects from the less intense sounds
from the profiler. Based upon the best available science, we believe
that the brief exposure of marine mammals to signals from the profiler
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.
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.''
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
[[Page 25979]]
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 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 we 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, we do 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
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).
The Observatory'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 the 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; observers posted during
operations scan the ocean for marine mammals and must report visual
alerts of marine mammal presence to crew; and the observers 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 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
[[Page 25980]]
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 the Foundation's Assessment).
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 sub-
lethal 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 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 the Foundation's Assessment). 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 temporary threshold shift 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
temporary threshold shift (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 low-frequency 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 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
(i.e., 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; 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
[[Page 25981]]
of the sound stimulus (see Appendix D of the Foundation's Assessment).
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. The Observatory will employ
avoidance tactics as necessary to prevent conflict. It is not expected
that the Observatory's operations will have a significant impact on
fisheries in the western Pacific Ocean. Nonetheless, the Observatory
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 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 the Foundation's Assessment).
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 in Appendix E of the Foundation's Assessment.
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 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 [mu]Pa. 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 sound pressure level was 157 v 5 dB re: 1 [mu]Pa,
with peak levels at 175 dB re: 1 [mu]Pa. 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 depend on numerous aspects of the
[[Page 25982]]
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 under section
101(a)(5)(D) of the Marine Mammal Protection Act, we 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.
The Observatory has based the mitigation measures which they will
implement during the proposed seismic survey, on the following:
(1) Protocols used during previous seismic research cruises as
approved by us;
(2) Previous incidental harassment authorizations applications and
authorizations that we have approved and authorized; 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
associated with the activities, the Observatory and/or its designees
would implement the following mitigation measures for marine mammals:
(1) Proposed exclusion zones;
(2) Power down procedures;
(3) Shutdown procedures; and
(4) Ramp-up procedures.
Proposed Exclusion Zones--The Observatory uses safety radii to
designate exclusion zones and to estimate take for marine mammals.
Table 2 (presented earlier in this document) shows the distances at
which one would expect to receive three sound levels (160-, 180-, and
190-dB) from the 36-airgun array and a single airgun. The 180-dB and
190-dB level shutdown criteria are applicable to cetaceans and
pinnipeds, respectively, as specified by us (2000). The Observatory
used these levels to establish the exclusion zones.
If the protected species visual observer detects marine mammal(s)
within or about to enter the appropriate exclusion zone, the Langseth
crew will immediately power down the airgun array, or perform a
shutdown if necessary (see Shut-down Procedures).
Power Down Procedures--A power down involves decreasing the number
of airguns in use such that the radius of the 180-dB (or 190-dB) zone
is smaller to the extent that marine mammals are no longer within or
about to enter the exclusion zone. 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, the Observatory 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 observer detects a marine mammal outside the exclusion zone
and the animal is likely to enter the zone, the crew will power down
the airguns to reduce the size of the 180-dB exclusion zone before the
animal enters that zone.
Likewise, if a mammal is already within the zone when first
detected, the crew will power-down the airguns immediately. During a
power down of the airgun array, the crew will operate a single 40-in\3\
airgun which has a smaller exclusion zone. If the observer detects a
marine mammal within or near the smaller exclusion zone around the
airgun (Table 2), the crew will shut down the single airgun (see next
section).
Shutdown Procedures--The Langseth crew will shutdown the operating
airgun(s) if a marine mammal is seen within or approaching the
exclusion zone for the single airgun. The crew will implement a
shutdown:
(1) If an animal enters the exclusion zone of the single airgun
after the crew has initiated a power down; or
(2) If an animal is initially seen within the exclusion zone of the
single airgun when more than one airgun (typically the full airgun
array) is operating.
Considering the conservation status for north Pacific right whales,
the Langseth crew will shutdown the airgun(s) immediately in the
unlikely event that this species is observed, regardless of the
distance from the vessel.
Resuming Airgun Operations After a Power Down
Following a power-down, the Langseth crew will not resume full
airgun activity until the marine mammal has cleared the 180-dB
exclusion zone (see Table 2). The observers will consider the animal to
have cleared the exclusion zone if:
The observer has visually observed the animal leave the
exclusion zone, or
An observer has not sighted the animal within the
exclusion zone for 15 minutes for species with shorter dive durations
(i.e., small odontocetes or pinnipeds), or 30 minutes 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 transited outside the original 180-dB
exclusion zone after an 8-minute wait period. This period is based on
the 180-dB exclusion zone for the 36-airgun array (940 m) towed at a
depth of 9 m (29.5 ft) in relation to the average speed of the Langseth
while operating the airguns (8.5 km/h; 5.3 mph).
The Langseth crew will resume operating the airguns at full power
after 15 minutes of sighting any species with short dive durations
(i.e., small odontocetes or pinnipeds). Likewise, the crew will resume
airgun operations at full power after 30 minutes of sighting any
species with longer dive durations (i.e., mysticetes and large
odontocetes, including sperm, pygmy sperm, dwarf sperm, and beaked
whales).
Because the vessel has transited 1.13 km (3,707 feet) away from the
vicinity of the original sighting during the 8-minute period,
implementing ramp-up procedures for the full array after an extended
power down (i.e., transiting for an additional 35 minutes from the
location of initial sighting) would not meaningfully increase the
effectiveness of observing marine mammals approaching or entering the
exclusion zone for the full source level and would
[[Page 25983]]
not further minimize the potential for take. The Langseth's observers
are continually monitoring the exclusion zone for the full source level
while the mitigation airgun is firing. On average, observers can
observe to the horizon (10 km; 6.2 mi) from the height of the
Langseth's observation deck and should be able to say with a reasonable
degree of confidence whether a marine mammal would be encountered
within this distance before resuming airgun operations at full power.
Resuming Airgun Operations After a Shutdown
Following a shutdown, the Langseth crew will initiate a ramp-up
with the smallest airgun in the array (40-in\3\). The crew will turn on
additional airguns in a sequence such that the source level of the
array will increase in steps not exceeding 6 dB per five-minute period
over a total duration of approximately 30 minutes. During ramp-up, the
observers will monitor the exclusion zone, and if he/she sights a
marine mammal, the Langseth crew will implement a power down or
shutdown as though the full airgun array were operational.
During periods of active seismic operations, there are occasions
when the Langseth crew will need to temporarily shut down the airguns
due to equipment failure or for maintenance. In this case, if the
airguns are inactive longer than eight minutes, the crew will follow
ramp-up procedures for a shutdown described earlier and the observers
will monitor the full exclusion zone and will implement a power down or
shutdown if necessary.
If the full exclusion zone is not visible to the observer for at
least 30 minutes prior to the start of operations in either daylight or
nighttime, the Langseth crew will not commence ramp-up unless at least
one airgun (40-in\3\ or similar) has been operating during the
interruption of seismic survey operations. Given these provisions, it
is likely that the vessel's crew will not ramp up the airgun array from
a complete shutdown at night or in thick fog, because the outer part of
the zone 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. The vessel's crew will not initiate a ramp-up of the airguns if a
marine mammal is sighted within or near the applicable exclusion zones
during the day or close to the vessel at night.
We have carefully evaluated the applicant's proposed mitigation
measures and have considered a range of other measures in the context
of ensuring that we have prescribed the means of effecting the least
practicable adverse impact on the affected marine mammal species and
stocks and their habitat. Our evaluation of potential measures included
consideration of the following factors in relation to one another:
(1) The manner in which, and the degree to which, we expect that
the successful implementation of the measure would 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 our evaluation of the Observatory's proposed measures, as
well as other measures considered by us or recommended by the public,
we have 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 grounds, and areas of similar
significance.
Proposed Monitoring and Reporting
In order to issue an incidental take authorization for an activity,
section 101(a)(5)(D) of the Marine Mammal Protection Act states that we
must set forth ``requirements pertaining to the monitoring and
reporting of such taking.'' The Act's implementing regulations at 50
CFR 216.104(a)(13) indicate that requests for an authorization must
include the suggested means of accomplishing the necessary monitoring
and reporting that will result in increased knowledge of the species
and our expectations of the level of taking or impacts on populations
of marine mammals present in the action area.
Proposed Monitoring
The Observatory proposes to sponsor marine mammal monitoring during
the present project, in order to implement the mitigation measures that
require real-time monitoring, and to satisfy the monitoring
requirements of the incidental harassment authorization. We describe
the Observatory's Monitoring Plan below this section. The Observatory
understands that this monitoring plan will be subject to review by us,
and that we may require refinements to the plan. The Observatory has
planned the monitoring work as a self-contained project independent of
any other related monitoring projects that may occur in the same
regions at the same time. Further, the Observatory would discuss
coordination of its monitoring program with any other related work by
other groups working in the same area, if practical.
Vessel-Based Visual Monitoring
The Observatory will position observers aboard the seismic source
vessel to watch for marine mammals near the vessel during daytime
airgun operations and during any start-ups at night. Observers will
also watch for marine mammals near the seismic vessel for at least 30
minutes prior to the start of airgun operations after an extended
shutdown (i.e., greater than approximately eight minutes for this
proposed cruise). When feasible, the observers 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 the
observations, the Langseth will power down or shutdown the airguns when
marine mammals are observed within or about to enter a designated
exclusion zone which is a region in which a possibility exists of
adverse effects on animal hearing or other physical effects.
During seismic operations, at least four protected species
observers will be aboard the Langseth. The Observatory will appoint the
observers with our concurrence. They will conduct observations during
ongoing daytime operations and nighttime ramp-ups of the airgun array.
During the majority of seismic operations, two observers will be on
duty from the observation tower to monitor marine mammals near the
seismic vessel. Using two observers will increase the effectiveness of
detecting animals near the source vessel. However, during mealtimes and
bathroom breaks, it is sometimes difficult to have two observers on
effort, but at least one observer will be on watch during bathroom
breaks and mealtimes. Observers will be on duty in shifts of no longer
than four hours in duration.
Two observers will also be on visual watch during all nighttime
ramp-ups of the seismic airguns. A third observer will monitor the
passive acoustic monitoring equipment 24 hours a day to detect
vocalizing marine mammals present in the action area. In summary, a
typical daytime cruise would have
[[Page 25984]]
scheduled two observers (visual) on duty from the observation tower,
and a observer (acoustic) on the passive acoustic monitoring system.
Before the start of the seismic survey, the Observatory will instruct
the vessel's crew to assist in detecting marine mammals and
implementing mitigation requirements.
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
observers will scan the area around the vessel systematically with
reticle binoculars (e.g., 7 x 50 Fujinon), Big-eye binoculars (25 x
150), and with the naked eye. During darkness, night vision devices
will be available (ITT F500 Series Generation 3 binocular-image
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 observers see marine mammals within or about to enter the
designated exclusion zone, the Langseth will immediately power down or
shutdown the airguns if necessary. The observer(s) will continue to
maintain watch to determine when the animal(s) are outside the
exclusion zone by visual confirmation. Airgun operations will not
resume until the observer has confirmed that the animal has left the
zone, or if not observed after 15 minutes for species with shorter dive
durations (small odontocetes and pinnipeds) or 30 minutes 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 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 acoustic observer will monitor the system in real
time so that he/she can advise the visual observers if they acoustic
detect cetaceans. When the acoustic observer determines the bearing
(primary and mirror-image) to calling cetacean(s), he/she alert the
visual observer to help him/her sight the calling animal(s).
The passive acoustic monitoring 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). The Langseth crew 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.
As described earlier, one acoustic observer, an expert
bioacoustician with primary responsibility for the passive acoustic
monitoring system will be aboard the Langseth in addition to the four
visual observers. The acoustic observer will monitor the towed
hydrophones 24 hours per day during airgun operations and during most
periods when the Langseth is underway while the airguns are not
operating. However, passive acoustic monitoring may not be possible if
damage occurs to both the primary and back-up hydrophone arrays during
operations. The primary passive acoustic monitoring 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 acoustic observer 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 observer monitoring the
acoustical data will be on shift for one to six hours at a time. The
other observers will rotate as an acoustic observer, although the
expert acoustician will be on passive acoustic monitoring duty more
frequently.
When the acoustic observer detects a vocalization while visual
observations are in progress, the acoustic observer on duty will
contact the visual observer immediately, to alert him/her to the
presence of cetaceans (if they have not already been seen), so that the
vessel's crew can initiate a power down or shutdown, if required. The
observer will enter the information regarding the call 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.
Observer Data and Documentation
Observers 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. They will use the data
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 exclusion zone.
When an observer makes a sighting, they will record the following
information:
1. Species, group size, age/size/sex categories (if determinable),
behavior 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 observer will record the data listed under (2) 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.
Observers will record all observations and power downs or shutdowns
in a standardized format and will enter data into an electronic
database. The
[[Page 25985]]
observers will verify the accuracy of the data entry by computerized
data validity checks as the data are entered and by subsequent manual
checking of the database. These procedures will allow the preparation
of initial summaries of data 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
shutdown).
2. Information needed to estimate the number of marine mammals
potentially taken by harassment, which the Observatory must report to
the Office of Protected Resources.
3. Data on the occurrence, distribution, and activities of marine
mammals and turtles in the area where the Observatory will conduct the
seismic study.
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
detected during non-active and active seismic operations.
Proposed Reporting
The Observatory will submit a report to us and to the Foundation
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 ``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
authorization (if issued), such as an injury (Level A harassment),
serious injury or mortality (e.g., ship-strike, gear interaction, and/
or entanglement), the Observatory shall immediately cease the specified
activities and immediately report the incident to the Incidental Take
Program Supervisor, Permits and Conservation Division, Office of
Protected Resources, NMFS, at 301-427-8401 and/or by email to
Jolie.Harrison@noaa.gov and ITP.Cody@noaa.gov and to the Northwest
Regional Stranding Coordinator at (206) 526-6550
(Brent.Norberg@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).
The Observatory shall not resume its activities until we are able
to review the circumstances of the prohibited take. We shall work with
the Observatory to determine what is necessary to minimize the
likelihood of further prohibited take and ensure Marine Mammal
Protection Act compliance. The Observatory may not resume their
activities until notified by us via letter, email, or telephone.
In the event that the Observatory discovers an injured or dead
marine mammal, and the lead visual observer 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 we describe in
the next paragraph), the Observatory will immediately report the
incident to the Incidental Take Program Supervisor, Permits and
Conservation Division, Office of Protected Resources, at 301-427-8401
and/or by email to Jolie.Harrison@noaa.gov and ITP.Cody@noaa.gov and to
the Northwest Regional Stranding Coordinator at (206) 526-6550
(Brent.Norberg@noaa.gov). The report must include the same information
identified in the paragraph above this section. Activities may continue
while we review the circumstances of the incident. We will work with
the Observatory to determine whether modifications in the activities
are appropriate.
In the event that the Observatory discovers an injured or dead
marine mammal, and the lead visual observer determines that the injury
or death is not associated with or related to the authorized activities
(e.g., previously wounded animal, carcass with moderate to advanced
decomposition, or scavenger damage), the Observatory will report the
incident to the Incidental Take Program Supervisor, Permits and
Conservation Division, Office of Protected Resources, at 301-427-8401
and/or by email to Jolie.Harrison@noaa.gov and ITP.Cody@noaa.gov and
the Northwest Regional Stranding Coordinator at (206) 526-6550
(Brent.Norberg@noaa.gov), within 24 hours of the discovery. The
Observatory will provide photographs or video footage (if available) or
other documentation of the stranded animal sighting to us.
Estimated Take by Incidental Harassment
Except with respect to certain activities not pertinent here, the
Marine Mammal Protection Act 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].
We propose to authorize take by Level B harassment only for the
proposed 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 re: 1 [mu]Pa or cause temporary, short-term changes
in behavior. There is no evidence that the Observatory's planned
activities could result in injury, serious injury or mortality within
the specified geographic area for the requested authorization. The
required mitigation and monitoring measures will minimize any potential
risk for injury, serious injury, or mortality.
The following sections describe the Observatory's methods to
estimate take by incidental harassment and present their estimates of
the numbers of marine mammals that could be affected during the
proposed seismic program. The Observatory's estimates assume that
marine mammals exposed to airgun sounds greater than or equal to 160 dB
re: 1 [micro]Pa might change their behavior sufficiently for us to
consider them as taken by harassment. They have based their estimates
on the number of marine mammals that could be disturbed appreciably by
operations with the 36-
[[Page 25986]]
airgun array during approximately 4,991 km (3,101.2 mi) of transect
lines in the northeastern Pacific Ocean.
We assume that during simultaneous operations of the airgun array
and the other sources, any marine mammals close enough to be affected
by the echosounder and sub-bottom profiler would already be affected by
the airguns. However, whether or not the airguns are operating
simultaneously with the other sources, we expect that the marine
mammals would exhibit no more than short-term and inconsequential
responses to the echosounder and profiler given their characteristics
(e.g., narrow downward-directed beam) and other considerations
described previously. Based on the best available information, we do
not consider that these reactions constitute a ``take'' (NMFS, 2001).
Therefore, the Observatory did not provide any additional allowance for
animals that could be affected by sound sources other than the airguns.
Ensonified Area Calculations--Because the Observatory assumes that
the Langseth may need repeat some tracklines, accommodate the turning
of the vessel, address equipment malfunctions, or conduct equipment
testing to complete the survey; they have increased the proposed number
of line-kilometers for the seismic operations by 25 percent (i.e.,
contingency lines).
The Observatory calculated the expected ensonified area by entering
the planned survey lines (including the 25 percent contingency lines)
into a Map-Info Geographic Information System (system). The Observatory
used the system to draw a 160-dB radius (see Table 2) around the
operating airgun array (i.e., the ensonified area) around each seismic
line. This first calculation is the area excluding overlap.
Depending on the spacing of the transect lines within the
ensonified area, the Observatory may also calculate areas of transit
overlap. For example, if the ratio of transit overlap is 1.5 times the
area excluding overlap, then the marine mammal that stayed within area
during the entire survey could be exposed to acoustic stimuli
approximately two times. However, it is unlikely that a particular
animal would stay in the area during the entire survey. For the Juan de
Fuca Survey, the transit lines are closely spaced together and the
ratio of transect overlap is 1.7 greater than the area excluding
overlapping transect lines. For the Cascadia Thrust Zone Survey the
ratio is 2.8, and for the Cascadia Subduction Margin Survey the ratio
is 2.0 times the area excluding overlap. Table 4 presents the area
calculations for each survey. Refer to the authorization application
and Assessment for additional information.
Table 4--Ensonified Area Calculations for Three Proposed Seismic Surveys in the Northeast Pacific Ocean, During
June-July 2012
----------------------------------------------------------------------------------------------------------------
Area Area with
excluding contingency Overlap
Survey overlap lines Transect line spacing ratio
(km\2\) (km\2\) (km\2\)
----------------------------------------------------------------------------------------------------------------
Juan de Fuca Plate......................... 18,471 23,089 Closely spaced................ 1.7
Cascadia Thrust Zone....................... 11,448 14,310 Closely spaced................ 2.8
Cascadia Subduction Margin................. 11,387 14,234 Closely spaced................ 2.0
----------------------------------------------------------------------------------------------------------------
Density Information--The Observatory calculated the density data
for 26 species reported off the Oregon and Washington coasts in the
northeastern Pacific Ocean using the following data sources:
Pooled results of the 1991-2008 NMFS Southwest Fishery
Science Center ship surveys as synthesized by Barlow and Forney (2007)
and Barlow (2010) for all species except the gray whale and harbor
porpoise.
Abundance estimates for gray whales that remain between
Oregon and B.C. in summer and the within area out to 43 km (26.7 mi)
from shore in the U.S. Navy's Keyport Range Complex Extension
Environmental Impact Statement/Overseas Environmental Impact Statement
(DoN, 2010); and
The population estimate for the Northern Oregon/Washington
Coast stock of harbor porpoises from the Pacific Marine Mammal Stock
Assessments 2010 Report (Carretta et al., 2010).
For the pooled results of the 1991-2008 NMFS Southwest Fishery
Science Center ship surveys, the Observatory has corrected the
densities for trackline detectability probability bias and availability
bias. Trackline detectability probability 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).
Exposure Calculations--The Observatory calculated the number of
different individuals that could be exposed to airgun sounds with
received levels greater than or equal to 160 dB re: 1 [micro]Pa by
multiplying the expected density of the marine mammals by the
ensonified area excluding areas of overlap. This area includes the 25
percent contingency lines.
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 [micro]Pa 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.
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 re: 1 [micro]Pa,
which will result in overestimates for those species known to avoid
seismic vessels.
Juan de Fuca Plate Survey Exposure Estimates
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 [mu]Pa during this survey is 10,208 (see Table 5). The
total includes 78 baleen whales, 56 of which are endangered: four blue
whales (0.17 percent of the regional population), 30 fin whales (0.18
percent of the regional population), 19 humpback whales (0.09 percent
of the regional population), and four sei whales (0.03 percent of the
[[Page 25987]]
population). In addition, 24 sperm whales (0.10 percent of the regional
population) and 303 Steller sea lions (0.46 percent of the population)
(both listed as endangered under the Endangered Species Act) could be
exposed during the survey.
Of the cetaceans potentially exposed, 57 percent are delphinids and
42 percent are pinnipeds. The most common species in the area
potentially exposed to sound levels greater than or equal to 160 dB re:
1 [mu]Pa during the proposed survey would be harbor porpoises (2,153 or
4.12 percent), Dall's porpoises (1,935 or 4.61 percent), northern fur
seals (1,931 or 0.30 percent), and northern elephant seals (1,058 or
0.85 percent).
Table 5--Estimates of the Possible Numbers of Marine Mammals Exposed to Sound Levels Greater Than or Equal to
160 dB re: 1 [mu]Pa During the Proposed Juan de Fuca Plate Seismic Survey in the Northeast Pacific Ocean, June-
July 2012
----------------------------------------------------------------------------------------------------------------
Estimated
number of
individuals Approximate
exposed to Requested or percent of
Species sound levels adjusted take regional
>=160 dB re: authorization population \2\
1 [micro]Pa
\1\
----------------------------------------------------------------------------------------------------------------
Gray whale...................................................... 10 10 0
Humpback whale.................................................. 19 19 0.09
Minke whale..................................................... 11 11 0.12
Sei whale....................................................... 4 4 0.03
Fin whale....................................................... 30 30 0.18
Blue whale...................................................... 4 4 0.17
Odontocetes
Sperm whale..................................................... 24 24 0.10
Pygmy/Dwarf sperm whale......................................... 16 16 N/A
Cuvier's beaked whale........................................... 10 10 0.46
Baird's beaked whale............................................ 27 27 3.0
Mesoplodon spp.\3\.............................................. 40 40 3.95
Striped dolphin................................................. 1 \4\ 2 0.01
Short-beaked common dolphin..................................... 237 \4\ 238 0.06
Pacific white-sided dolphin..................................... 806 806 299
Northern right whale dolphin.................................... 297 297 3.57
Risso's dolphin................................................. 258 258 4.12
Killer whale.................................................... 38 38 1.55
Harbor porpoise \5\............................................. 2,153 2,153 4.12
Dall's porpoise................................................. 1,935 1,935 4.61
Pinnipeds
Northern fur seal............................................... 1,931 1,931 0.30
Steller sea lion................................................ 303 303 0.46
Harbor seal \5\................................................. 995 995 4.02
Northern elephant seal.......................................... 1,058 1,058 0.85
----------------------------------------------------------------------------------------------------------------
N/A = Not Available
\1\ Estimates are based on densities in Table 3 and an ensonified area (including 25% contingency of 23,089
km\2\).
\2\ Regional population size estimates are from Table 3 (page 48 in Application 1).
\3\ Includes Blainville's, Stejneger's, and Hubb's beaked whales.
\4\ Requested take authorization increased to mean group size (see Application 1).
\5\ Estimates based on densities from Table 3 (page 48 in Application 1) and an ensonified area in
water depths less than 100 m (328 ft) (including 25 percent contingency) of 3,404 km.\2\
Cascadia Thrust Zone Survey Exposure Estimates
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 [mu]Pa during this survey is 15,100 (see Table 6). The
total includes 79 baleen whales, 35 of which are endangered: Three blue
whales (0.10 percent of the regional population), 18 fin whales (0.11
percent of the regional population), 12 humpback whales (0.06 percent
of the regional population), and two sei whales (0.02 percent of the
population). In addition, 15 sperm whales (0.06 percent of the regional
population) and 188 Steller sea lions (0.29 percent of the population)
(both listed as endangered under the Endangered Species Act) could be
exposed during the survey.
Of the cetaceans potentially exposed, 63 percent are delphinids and
36 percent are pinnipeds. The most common species in the area
potentially exposed to sound levels greater than or equal to 160 dB re:
1 [micro]Pa during the proposed survey would be Dall's porpoises (1,199
or 2.86 percent), harbor porpoises (7,314 or 14 percent of the regional
population or 9.2 percent of the overall population), and harbor seals
(3,380 or 13.67 percent of the regional population or 4.6% of the
overall population) and northern fur seals (1,197 or 0.18 percent)
(Allen and Angliss, 2011). The percentages for harbor porpoises and
harbor seals are the upper boundaries of the regional populations that
could be affected by the proposed survey. However, these take estimates
are small relative to the overall population sizes for each species in
the northeast Pacific. Thus, these take estimates are likely an
overestimate of the actual number of animals that may be taken by Level
B harassment and we expect that the actual number of individual animals
that may be taken by Level B harassment to be less than the request.
[[Page 25988]]
Table 6--Estimates of the Possible Numbers of Marine Mammals Exposed to Sound Levels Greater Than or Equal to
160 dB re: 1 [mu]Pa During the Proposed Cascadia Thrust Zone Seismic Survey in the Northeast Pacific Ocean, July
2012
----------------------------------------------------------------------------------------------------------------
Estimated
number of
individuals Requested or Approximate
Species exposed to adjusted take percent of
sound levels authorization regional
>=160 dB re: 1 population \2\
[mu]Pa \1\
----------------------------------------------------------------------------------------------------------------
Gray whale...................................................... 35 35 0.18
Humpback whale.................................................. 12 12 0.06
Minke whale..................................................... 7 7 0.07
Sei whale....................................................... 2 2 0.02
Fin whale....................................................... 18 18 0.11
Blue whale...................................................... 3 3 0.10
Odontocetes
Sperm whale..................................................... 15 15 0.06
Pygmy/Dwarf sperm whale......................................... 10 10 NA
Cuvier's beaked whale........................................... 6 6 0.28
Baird's beaked whale............................................ 17 17 1.86
Mesoplodon spp.\3\.............................................. 25 25 2.45
Striped dolphin................................................. 1 \4\ 2 <0.01
Short-beaked common dolphin..................................... 147 \4\ 238 0.04
Pacific white-sided dolphin..................................... 500 500 1.86
Northern right whale dolphin.................................... 184 184 2.21
Risso's dolphin................................................. 160 160 2.55
Killer whale.................................................... 24 24 0.96
Harbor porpoise \5\............................................. 7,314 7,314 14.00
Dall's porpoise................................................. 1,199 1,199 2.86
Pinnipeds
Northern fur seal............................................... 1,197 1,197 0.18
Steller sea lion................................................ 188 188 0.29
Harbor seal \5\................................................. 3,380 3,380 13.67
Northern elephant seal.......................................... 656 656 0.53
----------------------------------------------------------------------------------------------------------------
N/A = Not Available.
\1\ Estimates are based on densities in Table 3 and an ensonified area (including 25% contingency of 14,310
km\2\).
\2\ Regional population size estimates are from Table 3 (page 47 in Application 2).
\3\ Includes Blainville's, Stejneger's, and Hubb's beaked whales.
\4\ Requested take authorization increased to mean group size (see Application 2).
\5\ Estimates based on densities from Table 3 (page 47 in Application 2) and an ensonified area in
water depths less than 100 m (328 ft) (including 25 percent contingency) of 11.565 km\2\.
Cascadia Subduction Margin Survey Exposure Estimates
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 [mu]Pa during this survey is 8,132 (see Table 7). The
total includes 54 baleen whales, 35 of which are endangered: three blue
whales (0.10 percent of the regional population), 18 fin whales (0.11
percent of the regional population), 11 humpback whales (0.06 percent
of the regional population), and two sei whales (0.02 percent of the
population). In addition, 15 sperm whales (0.06 percent of the regional
population) and 187 Steller sea lions (0.29 percent of the population)
(both listed as endangered under the Endangered Species Act) could be
exposed during the survey.
Of the cetaceans potentially exposed, 59 percent are delphinids and
40 percent are pinnipeds. The most common species in the area
potentially exposed to sound levels greater than or equal to 160 dB re:
1 [mu]Pa during the proposed survey would be harbor porpoises (2,580 or
4.94 percent), Dall's porpoises (1,193 or 2.84 percent), northern fur
seals (1,190 or 0.18 percent), and harbor seals (1,192 or 4.82
percent).
Table 7--Estimates of the Possible Numbers of Marine Mammals Exposed to Sound Levels Greater Than or Equal to
160 dB re: 1 [mu]Pa During the Proposed Cascadia Subduction Margin Seismic Survey in the Northeast Pacific
Ocean, July 2012
----------------------------------------------------------------------------------------------------------------
Estimated
number of
individuals Requested or Approximate
Species exposed to adjusted take percent of
sound levels authorization regional
>=160 dB re: population \2\
1 [mu]Pa\1\
----------------------------------------------------------------------------------------------------------------
Gray whale...................................................... 12 12 0.06
Humpback whale.................................................. 11 11 0.06
[[Page 25989]]
Minke whale..................................................... 6 6 0.07
Sei whale....................................................... 2 2 0.02
Fin whale....................................................... 18 18 0.11
Blue whale...................................................... 3 3 0.10
Odontocetes
Sperm whale..................................................... 15 15 0.06
Pygmy/Dwarf sperm whale......................................... 10 10 NA
Cuvier's beaked whale........................................... 6 6 0.28
Baird's beaked whale............................................ 17 17 1.85
Mesoplodon spp.\3\.............................................. 25 25 2.44
Striped dolphin................................................. 1 \4\ 2 <0.01
Short-beaked common dolphin..................................... 146 \4\ 238 0.04
Pacific white-sided dolphin..................................... 497 497 1.85
Northern right whale dolphin.................................... 183 183 2.20
Risso's dolphin................................................. 159 159 2.54
Killer whale.................................................... 24 24 0.96
Harbor porpoise \5\............................................. 2,580 2,580 4.94
Dall's porpoise................................................. 1,193 1,193 2.84
Pinnipeds
Northern fur seal............................................... 1,190 1,190 0.18
Steller sea lion................................................ 187 187 0.29
Harbor seal \5\................................................. 1,192 1,192 4.82
Northern elephant seal.......................................... 652 652 0.53
----------------------------------------------------------------------------------------------------------------
N/A = Not Available.
\1\ Estimates are based on densities in Table 3 and an ensonified area (including 25% contingency of 14,234
km\2\).
\2\ Regional population size estimates are from Table 3 (page 47 in Application 3).
\3\ Includes Blainville's, Stejneger's, and Hubb's beaked whales.
\4\ Requested take authorization increased to mean group size (see Application 3).
\5\ Estimates based on densities from Table 3 (page 47 in Application 3) and an ensonified area in
water depths less than 100 m (328 ft) (including 25 percent contingency) of 4,080 km\2\.
Encouraging and Coordinating Research
The Observatory and the Foundation will coordinate the planned
marine mammal monitoring program associated with each seismic survey in
the northwestern Pacific Ocean with other parties that may have
interest in the area and/or may be conducting marine mammal studies in
the same region during the seismic surveys.
Negligible Impact and Small Numbers Analysis and Determination
We have 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,
we consider:
(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 surveys are not likely to
cause permanent threshold shift, or other non-auditory injury, serious
injury, or death because:
(1) The likelihood that, given sufficient notice through relatively
slow ship speed, we expect marine mammals 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 that we would likely avoid this impact 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, 1,540 m (5,052 ft) in intermediate depths,
and 2,140 m (7,020 ft) in shallow depths, when the 36-airgun array is
in use at 9 m (29.5 ft) tow depth from the vessel to be exposed to
levels of sound believed to have a minimal chance of causing permanent
threshold shift;
(4) The fact that cetaceans would have to be closer than 1,100 m
(3,609 ft) in deep water, 1,810 m (5,938 ft) in intermediate depths,
and 2,520 m (8,268 ft) in shallow depths, when the 36-airgun array is
in use at 12 m (39.4 ft) tow depth from the vessel to be exposed to
levels of sound believed to have a
[[Page 25990]]
minimal chance of causing permanent threshold shift;
(5) The fact that cetaceans would have to be closer than 1,200 m
(3,937 ft) in deep water, 1,975 m (6,480 ft) in intermediate depths,
and 2,750 m (9,022 ft) in shallow depths, when the 36-airgun array is
in use at 15 m (49.2 ft) tow depth from the vessel to be exposed to
levels of sound believed to have a minimal chance of causing permanent
threshold shift;
(6) The fact that cetaceans would have to be closer than 40 m (131
ft) in deep water, 60 m (197 ft) in intermediate depths, and 296 m (971
ft) in shallow depths, when the single airgun is in use at six to 15 m
(20 to 49.2 ft) tow depth from the vessel to be exposed to levels of
sound believed to have a minimal chance of causing permanent threshold
shift;
(7) The fact that pinnipeds would have to be closer than 400 m
(1,312 ft) in deep water, 550 m (1,804 ft) in intermediate depths, and
680 m (2,231 ft) in shallow depths, when the 36-airgun array is in use
at 9 m (29.5 ft) tow depth from the vessel to be exposed to levels of
sound believed to have a minimal chance of causing permanent threshold
shift;
(8) The fact that pinnipeds would have to be closer than 460 m
(1,509 ft) in deep water, 615 m (2,018 ft) in intermediate depths, and
770 m (2,526 ft) in shallow depths, when the single airgun is in use at
12 m (39.4 ft) tow depth from the vessel to be exposed to levels of
sound believed to have a minimal chance of causing permanent threshold
shift;
(9) The fact that pinnipeds would have to be closer than 520 m
(1,706 ft) in deep water, 690 m (2,264 ft) in intermediate depths, and
865 m (2,838 ft) in shallow depths, when the single airgun is in use at
15 m (49.2 ft) tow depth from the vessel to be exposed to levels of
sound believed to have a minimal chance of causing permanent threshold
shift;
(10) The fact that pinnipeds would have to be closer than 12 m
(39.4 ft) in deep water, 18 m (59 ft) in intermediate depths, and 150 m
(492 ft) in shallow depths, when the single airgun is in use at six to
15 m (20 to 49.2 ft) tow depth from the vessel to be exposed to levels
of sound believed to have a minimal chance of causing permanent
threshold shift; and
(11) The likelihood that marine mammal detection ability by trained
visual observers is high at close proximity to the vessel.
We do not anticipate that any injuries, serious injuries, or
mortalities would occur as a result of the Observatory's planned marine
seismic surveys, and we do not propose to authorize injury, serious
injury or mortality for this survey. We anticipate only short-term
behavioral disturbance to occur during the conduct of the survey
activities. Tables 5, 6, and 7 of this document outline the number of
requested Level B harassment takes that we anticipate 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), we do not expect
the activity to impact rates of recruitment or survival for any
affected species or stock. Further, the seismic surveys would not take
place in areas of significance for marine mammal feeding, resting,
breeding, or calving and would 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 hour 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 we anticipate
that the seismic operations would occur on consecutive days, the
estimated duration of the Juan de Fuca Plate survey would last no more
than 17 days, the Cascadia Thrust Zone survey would last approximately
three days, and the Cascadia Subduction Margin survey would occur over
10 days.
Because the Langseth will move continuously along planned
tracklines, each seismic survey would increase sound levels in the
marine environment surrounding the vessel for 21 days during the first
and second study and for 10 days during the last study. There will be
an estimated 4-day period of non-seismic activity between the second
and third survey.
Of the 31 marine mammal species under our jurisdiction that are
known to occur or likely to occur in the study area, six of these
species and two stocks are listed as endangered under the Endangered
Species Act: The blue, fin, humpback, north Pacific right, sei, and
sperm whales; the southern resident stock of killer whales; and the
eastern U.S. stock of the Steller sea lion. These species are also
categorized as depleted under the Marine Mammal Protection Act. With
the exception of North Pacific right whales, the Observatory has
requested authorized take for these listed species. To protect these
animals (and other marine mammals in the study area), the Observatory
must cease or reduce airgun operations if animals enter designated
zones.
Based on available data, we do not expect the Observatory to
encounter five of the 31 species under our jurisdiction in the proposed
survey areas. They include the following: The north Pacific right,
false killer, and short-finned pilot whales; the California sea lion;
and the bottlenose dolphin because of the species' rare and/or
extralimital occurrence in the survey areas. As mentioned previously,
we estimate that 26 species of marine mammals under our jurisdiction
could be potentially affected by Level B harassment over the course of
the proposed authorization. For each species, these numbers are small,
relative to the regional or overall population size and we have
provided the regional population estimates for the marine mammal
species that may be taken by Level B harassment in Tables 5, 6, and 7
in this document. Our practice has been to apply the 160 dB re: 1
[micro]Pa 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]).
We have preliminarily determined, provided that the aforementioned
mitigation and monitoring measures are implemented, that the impact of
conducting three marine seismic surveys off Oregon and Washington in
the northwestern Pacific Ocean, June through July, 2012, may result, at
worst, in a temporary modification in behavior and/or low-level
physiological effects (Level B harassment) of small numbers of certain
species of marine mammals. See Tables 5, 6, and 7 for the requested
authorized take numbers of cetaceans.
While these species may make behavioral modifications, including
temporarily vacating the area during the operation of the airgun(s) to
avoid the resultant acoustic disturbance, the availability of alternate
areas within these areas and the short duration of the research
activities, have led us to preliminarily 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, we preliminarily find that the Observatory's
[[Page 25991]]
planned research activities will result in the incidental take of small
numbers of marine mammals, by Level B harassment only, and that the
required measures mitigate impacts to affected species or stocks of
marine mammals to the lowest level practicable.
Impact on Availability of Affected Species or Stock for Taking for
Subsistence Uses
Section 101(a)(5)(D) of the Marine Mammal Protection Act also
requires us 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 (northeastern Pacific Ocean) that
implicate section 101(a)(5)(D) of the Marine Mammal Protection Act.
Endangered Species Act
Of the species of marine mammals that may occur in the proposed
survey area, several are listed as endangered under the Endangered
Species Act, including the blue, fin, humpback, north Pacific right,
sei, and sperm whales. The Observatory did not request take of
endangered north Pacific right whales because of the low likelihood of
encountering these species during the cruise.
Under section 7 of the Act, the Foundation has initiated formal
consultation with the Service's, Office of Protected Resources,
Endangered Species Act Interagency Cooperation Division, on this
proposed seismic survey. We (i.e., National Marine Fisheries Service,
Office of Protected Resources, Permits and Conservation Division), have
also initiated formal consultation under section 7 of the Act with the
Endangered Species Act Interagency Cooperation Division to obtain a
Biological Opinion (Opinion) evaluating the effects of issuing an
incidental harassment authorization for threatened and endangered
marine mammals and, if appropriate, authorizing incidental take. We
will conclude the formal section 7 consultation prior to making a
determination on whether or not to issue the authorization. If we issue
the take authorization, the Foundation and the Observatory must comply
with the Terms and Conditions of the Opinion's Incidental Take
Statement in addition to the mitigation and monitoring requirements
included in the issued take authorization.
National Environmental Policy Act (NEPA)
With its complete application, the Foundation and the Observatory
provided an ``Environmental Assessment and Finding of No Significant
Impact Determination Pursuant to the National Environmental Policy Act,
(NEPA: 42 U.S.C. 4321 et seq.) and Executive Order 12114 for a ``Marine
Seismic Survey in the northeastern Pacific Ocean, 2012,'' which
incorporates an ``Environmental Assessment of a Marine Geophysical
Survey by the R/V Marcus G. Langseth in the northeastern Pacific Ocean,
June-July 2012,'' prepared by LGL Limited environmental research
associates.
The Assessment analyzes the direct, indirect, and cumulative
environmental impacts of the specified activities on marine mammals
including those listed as threatened or endangered under the Endangered
Species Act. We have conducted an independent review and evaluation of
the document for sufficiency and compliance with the Council of
Environmental Quality and NOAA Administrative Order 216-6 Sec.
5.09(d), Environmental Review Procedures for Implementing the National
Environmental Policy Act, and have preliminarily determined that
issuance of the incidental harassment authorization is not likely to
result in significant impacts on the human environment. Consequently,
we plan to adopt the Foundation's Assessment and intend to prepare a
Finding of No Significant Impact for the issuance of the authorization.
Proposed Authorization
As a result of these preliminary determinations, we propose to
authorize the take of marine mammals incidental to the Observatory's
proposed marine seismic surveys in the northeast Pacific Ocean,
provided the previously mentioned mitigation, monitoring, and reporting
requirements are incorporated. The duration of the incidental
harassment authorization would not exceed one year from the date of its
issuance.
Information Solicited
We request interested persons to submit comments and information
concerning this proposed project and our preliminary determination of
issuing a take authorization (see ADDRESSES). Concurrent with the
publication of this notice in the Federal Register, we will forward
copies of this application to the Marine Mammal Commission and its
Committee of Scientific Advisors.
Dated: April 27, 2012.
Helen M. Golde,
Acting Director, Office of Protected Resources, National Marine
Fisheries Service.
[FR Doc. 2012-10627 Filed 5-1-12; 8:45 am]
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