Takes of Marine Mammals Incidental to Specified Activities; Marine Geophysical Survey on the Mid-Atlantic Ridge in the Atlantic Ocean, April 2013, Through June 2013, 10137-10160 [2013-03321]
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Federal Register / Vol. 78, No. 30 / Wednesday, February 13, 2013 / Notices
monitoring program and eliminate the
requirement for dockside monitoring for
both sector and common pool vessels.
As this measure has not yet been
approved, and a sector may elect to
retain dockside monitoring through its
operations plan, NMFS is also
approving dockside monitoring service
providers.
Approved Monitoring Service Providers
and provided dockside and/or at-sea
monitoring services to sectors. The
Regional Administrator has approved
the following service providers as
eligible to provide dockside monitoring
and/or at-sea monitoring services in FY
2013:
NMFS received complete applications
from three service providers intending
to provide dockside and/or at-sea
monitoring services, and one service
provider intending to provide only atsea monitoring services. All four
applicants were previously approved
TABLE 1—APPROVED FY 2013 PROVIDERS
Provider name
At-Sea
monitoring
Dockside
monitoring
Address
Phone
Fax
A.I.S., Inc .......
X
X
(508) 990–9054
(508) 990–9055
www.aisobservers.com
MRAG Americas.
Atlantic Catch
Data Ltd..
X
X
(978) 768–3880
(978) 768–3878
www.mragamericas.com
X
X
(902) 422–4745
(902) 422–9780
www.atlanticcatchdata.ca
....................
X
89 North Water Street, New
Bedford, MA 02747.
65 Eastern Ave., Unit B2C,
Essex, MA 01929.
99 Wyse Road, Suite 815,
Dartmouth, Nova Scotia,
CANADA B3A 4S5.
34 Batterson Drive, New Britain, CT 06053.
(860) 223–5165
(860) 223–6005
www.ewts.com
East West
Technical
Services,
LLC.
Authority: 16 U.S.C. 1801 et seq.
Dated: February 8, 2013.
Kara Meckley,
Acting Deputy Director, Office of Sustainable
Fisheries, National Marine Fisheries Service.
[FR Doc. 2013–03371 Filed 2–12–13; 8:45 am]
BILLING CODE 3510–22–P
DEPARTMENT OF COMMERCE
RIN 0648–XC238
Takes of Marine Mammals Incidental to
Specified Activities; Marine
Geophysical Survey on the MidAtlantic Ridge in the Atlantic Ocean,
April 2013, Through June 2013
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 (Observatory), in
collaboration with the National Science
Foundation (Foundation), for an
Incidental Harassment Authorization to
take marine mammals, by harassment,
incidental to conducting a marine
geophysical (seismic) survey on the
Mid-Atlantic Ridge in the north Atlantic
Ocean in international waters, from
April 2013 through May 2013. Per the
Marine Mammal Protection Act, we are
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Comments on the
application should be addressed to P.
Michael Payne, Chief, Permits and
Conservation Division, Office of
Protected Resources, National Marine
Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910–
3225. The mailbox address for providing
email comments is ITP.Cody@noaa.gov.
Please include 0648–XC238 in the
subject line. We are not responsible for
email comments sent to other addresses
other than the one provided here.
Comments sent via email to
ITP.Cody@noaa.gov, including all
attachments, must not exceed a 10megabyte 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, write to the previously
mentioned address, telephone the
ADDRESSES:
National Oceanic and Atmospheric
Administration
SUMMARY:
requesting comments on our proposal to
issue an Incidental Harassment
Authorization to the Observatory and
the Foundation to incidentally harass by
Level B harassment only, 28 species of
marine mammals during the 20-day
seismic survey.
DATES: Comments and information must
be received no later than March 15,
2013.
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Web site
contact listed here (see FOR FURTHER
or visit the
internet at: https://www.nmfs.noaa.gov/
pr/permits/incidental.htm#applications.
The following associated documents
are also available at the same internet
address:
The Foundation’s draft environmental
analysis titled, ‘‘Marine geophysical
survey by the R/V MARCUS G.
LANGSETH on the mid-Atlantic Ridge,
April–May 2013,’’ for their federal
action of funding the Observatory’s
seismic survey. LGL Ltd.,
Environmental Research Associates
(LGL), prepared this analysis on behalf
of the Foundation pursuant to Executive
Order 12114: Environmental Effects
Abroad of Major Federal Actions. The
Foundation’s environmental analysis
evaluates the effects of the proposed
seismic survey on the human
environment including impacts to
marine mammals. We will prepare a
separate National Environmental Policy
Act (NEPA: 42 U.S.C. 4321 et seq.)
analysis to evaluate the environmental
effects related to the scope of our federal
action which is the proposed issuance
of an incidental take authorization to
the Observatory and the Foundation. We
plan to incorporate the Foundation’s
environmental analysis, in whole or
part, by reference, into our NEPA
document as that analysis provides a
detailed description of the planned
survey and its anticipated effects on
marine mammals. This notice and the
referenced document present detailed
information on the scope of our federal
action under NEPA (i.e., potential
impacts to marine mammals from
INFORMATION CONTACT),
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issuing the proposed IHA including
measures for mitigation, and
monitoring) and we will consider
comments submitted in response to this
notice as we prepare our NEPA analysis.
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, National Marine
Fisheries Service, Office of Protected
Resources, (301) 427–8401.
SUPPLEMENTARY INFORMATION:
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Background
Section 101(a)(5)(D) of the Marine
Mammal Protection Act of 1972, as
amended (MMPA; 16 U.S.C. 1361 et
seq.) directs the Secretary of Commerce
to authorize, upon request, the
incidental, but not intentional, taking of
small numbers of marine mammals of a
species or population stock, by United
States citizens who engage in a specified
activity (other than commercial fishing)
within a specified geographical region
if, after notice of a proposed
authorization to the public for review
and public comment: (1) We make
certain findings; and (2) the taking is
limited to harassment.
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 taking. 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 MMPA
established an expedited process by
which citizens of the United States can
apply for an authorization to
incidentally take small numbers of
marine mammals by harassment.
Section 101(a)(5)(D) of the MMPA
establishes a 45-day time limit for 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
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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 MMPA
defines ‘‘harassment’’ as: any act of
pursuit, torment, or annoyance which (i)
has the potential to injure a marine
mammal or marine mammal stock in the
wild [Level A harassment]; or (ii) has
the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment].
Summary of Request
We received an application from the
Observatory on December 7, 2012,
requesting that we issue an Incidental
Harassment Authorization
(Authorization) for the take, by Level B
harassment only, of small numbers of
marine mammals incidental to
conducting a marine seismic survey in
the north Atlantic Ocean in
international waters from April 8, 2013,
through May 13, 2013. We received a
revised application from the
Observatory on December 23, 2012 and
January 17, 2013, which reflected
updates to the mitigation safety zones,
incidental take requests for marine
mammals, and information on marine
protected areas. Upon receipt of
additional information, we determined
the application complete and adequate
on January 18, 2013.
Project Purpose—The Observatory
plans to conduct a two-dimensional (2–
D) seismic survey on the Mid-Atlantic
Ridge in the north Atlantic Ocean.
Specifically, the proposed survey would
image the Rainbow massif to determine
the characteristics of the magma body
that supplies heat to the Rainbow
hydrothermal field; determine the
distribution of the different rock types
that form the Rainbow massif; document
large- and small-scale faults in the
vicinity and investigate their role in
controlling hydrothermal fluid
discharge.
Vessel—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 (seismometers) to conduct
the seismic survey. In addition to the
operations of the seismic airgun array
and hydrophone streamer, and the
seismometers, the Observatory intends
to operate a multibeam echosounder
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and a sub-bottom profiler continuously
throughout the proposed survey.
Marine Mammal Take—Acoustic
stimuli (i.e., increased underwater
sound) generated during the operation
of the seismic airgun arrays, may have
the potential to cause behavioral
disturbance for marine mammals in the
survey area. This is the principal means
of marine mammal take associated with
these activities and the Observatory
requested an authorization to take 28
species of marine mammals by Level B
harassment.
In the Observatory’s application, they
did not request authorization to take
marine mammals by Level A
Harassment because their
environmental analyses estimate that
marine mammals would not be exposed
to levels of sound likely to result in
Level A harassment (we refer the reader
to Appendix B of the Foundation’s
NEPA document titled, ‘‘2011 Final
Programmatic Environmental Impact
Statement/Overseas Environmental
Impact Statement (2011 PEIS) for
Marine Seismic Research funded by the
National Science Foundation or
Conducted by the U.S. Geological
Survey,’’ (NSF/USGS, 2011) at https://
www.nsf.gov/geo/oce/envcomp/usgsnsf-marine-seismic-research/nsf-usgsfinal-eis-oeis-with-appendices.pdf for
details). Consequently, the
Observatory’s request for take by Level
A harassment is zero animals for any
species.
We do not expect that the use of the
multibeam echosounder, the sub-bottom
profiler, or the ocean bottom
seismometer would 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 during
seismic acquisition activities because
the vessel moves at a relatively slow
speed (approximately 8.3 kilometers per
hour (km/h); 5.2 miles per hour (mph);
4.5 knots (kts)), for a relatively short
period of time (approximately 20
operational days). It is likely that any
marine mammal would be able to avoid
the vessel during seismic acquisition
activities. The Observatory has no
recorded cases of a vessel strike with a
marine mammal during the conduct of
over eight years of seismic surveys
covering over 160,934 km (86,897.4
nmi) of transect lines.
Description of the Proposed Specified
Activities
Survey Details
The Observatory’s proposed seismic
survey on the Mid-Atlantic Ridge in the
north Atlantic Ocean would commence
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on April 8, 2013, and end on May 13,
2013. The LANGSETH would depart
from St. George’s, Bermuda, on April 8,
2013, and transit to the proposed survey
area in international waters
approximately 300 km (186.4 miles
(mi)) offshore of Pico and Faial Islands
in the Azores. At the conclusion of the
proposed survey activities, the
LANGSETH would arrive in Ponta
Delgada, Azores on May 13, 2012. The
proposed study area would encompass
an area on the Mid-Atlantic Ridge
bounded by the following coordinates:
Approximately 35.5 to 36.5° North by
33.5 to 34.5° West.
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 that is effective
from April 8, 2013, to June 24, 2013.
Typically, 2–D surveys 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 the survey, the
LANGSETH would deploy an 36-airgun
array as an energy source, an 8kilometer (km)-long (3.7 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.
The LANGSETH would transect
approximately 2,582 km (1.6 mi) of
transect lines which are spaced 1 to 2
meters (m) (3.2 to 6.6 feet (ft)) apart from
one another (see Figure 1 in the
Observatory’s application). As the
LANGSETH tows the airgun array along
the transect lines, the hydrophone
streamer would receive the returning
acoustic signals and transfer the data to
the vessel’s onboard processing system.
The seismometers also record and store
the returning signals for later analysis.
The LANGSETH would retrieve the
seismometers at the conclusion of the
survey.
The proposed study (e.g., equipment
testing, startup, line changes, repeat
coverage of any areas, and equipment
recovery) would require approximately
20 days. At the proposed survey area,
the LANGSETH would conduct seismic
acquisition activities in a grid pattern
using the seismometers as a receiver
over a total of approximately 1,680 km
(1,044 mi) of survey lines and would
also conduct seismic acquisition
activities in multichannel seismic
(MCS) mode using the 8-km (3.7 mi)
streamer as the receiver over a total of
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approximately 900 km (559 mi). The
seismic lines are over water depths of
approximately 900 to 3,000 m (2,952 ft
to 1.9 mi). Approximately 2,565 km
(1,594 mi) of the survey effort would
occur in depths greater than 1,000 m
(3,280 ft). The remaining effort (17 km;
10.5 mi) would occur in water depths of
100 to 1,000 m (328 to 3,280 ft).
The proposed data acquisition would
include approximately 480 hours of
airgun operations (i.e., 20 days over 24
hours), with airgun discharges occurring
on either a 3.25 minute interval with the
seismometers or a 16-second interval for
the MCS seismic portion. The
Observatory would conduct all planned
seismic activities with on-board
assistance by the scientists who have
proposed the study, Drs. J.P. Canales
and R. Sohn of Woods Hole
Oceanographic Institution and Dr. R.
Dunn of the University of Hawaii. The
vessel is self-contained and the crew
would live aboard the vessel for the
entire cruise.
Vessel Specifications
R/V LANGSETH
The LANGSETH, owned by the
Foundation and operated by the
Observatory, 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. Its 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 cruising speed
of the vessel outside of seismic
operations is 18.5 km/h (11.5 mph; 10
kts).
The LANGSETH would tow the 36airgun 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) would watch
for marine mammals before and during
the proposed seismic acquisition
operations. When stationed on the
observation platform, the observer’s eye
level would be approximately 21.5 m
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10139
(71 ft) above sea level providing the
observer an unobstructed view around
the entire vessel.
Acoustic Source Specifications
Seismic Airguns
The LANGSETH would deploy an 36airgun array, with a total volume of
approximately 6,600 cubic inches (in3).
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 first
and last airguns would be spaced 16 m
(52 ft) apart. Of the 10 airguns, nine
would fire simultaneously while the
tenth airgun would serve as a spare in
case of failure of one of the other
airguns. The LANGSETH would
distribute the array across an area of
approximately 24 x 16 m (78.7 x 52.5 ft)
and would tow the array approximately
30 m (98.4 ft) behind the vessel at a tow
depth of 12 m (39.4 ft) (see Figure 2–11,
page 2–25 in the Foundation’s 2011
PEIS) (NSF/USGS, 2011). During firing,
the airguns would 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. 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 mPa,
and the units for sound pressure levels
are dB re: 1 mPa. Sound pressure level
(in decibels (dB)) = 20 log (pressure/
reference pressure).
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
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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 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
predicted the received sound levels in
relation to distance and direction from
the 36-airgun array and the single Bolt
1900LL 40-in3 airgun.
Appendix H of the Foundation’s PEIS
(NSF/USGS, 2011) provides a detailed
description of the modeling for marine
seismic source arrays for species
mitigation. 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. We refer
the reader to the Observatory’s
authorization application and the
Foundation’s PEIS for additional
information.
Predicted Sound Levels for the Airguns
The Observatory has developed a
model (Diebold et al., 2010) that
predicts received sound levels as a
function of distance from the airguns for
the 36-airgun array and the single 40-in3
airgun. Their modeling approach uses
ray tracing (i.e., a graphical
representation of the effects of refracting
sound waves) for the direct wave
traveling from the array to the receiver
and its associated source ghost
(reflection at the air-water interface in
the vicinity of the array), in a constantvelocity half-space (infinite
homogeneous ocean layer, unbounded
by a seafloor).
Additionally, Tolstoy et al., (2009)
reported results for propagation
measurements of pulses from the
LANGSETH’s 36-airgun 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
their algorithm for acoustic modeling
(Diebold et al., 2010) to calculate the
exclusion zones for the 36-airgun array
and the single airgun. These values
designate mitigation zones used during
power downs or shutdowns for marine
mammals. The Observatory uses the
mitigation zones to estimate take
(described in greater detail in Chapter 7
of the application) for marine mammals.
Comparison of the Tolstoy et al.
(2009) calibration study with the
Observatory’s model (Diebold et al.,
2010) for the LANGSETH’s 36-airgun
array indicated that the Observatory’s
model represents the actual received
levels, within the first few kilometers
and the locations of the predicted
exclusions zones. Thus, the comparison
of results from the Tolstoy et al. (2009)
calibration study with the Observatory’s
model (Diebold et al., 2010) at short
ranges for the same array tow depth are
in good agreement (see Figures 12 and
14 in Diebold et al., 2010). As a
consequence, isopleths falling within
this domain can be predicted reliably by
the Observatory’s model.
In contrast, for actual received levels
at longer distances, the Observatory
found that their model (Diebold et al.,
2010) was a more robust tool for
estimating mitigation radii in deep
water as it did not overestimate the
received sound levels at a given
distance. To estimate mitigation radii in
intermediate water depths, the
Observatory applied a correction factor
(multiplication) of 1.5 to the deep water
mitigation radii. We refer the reader to
Appendix H of the Foundation’s PEIS
(NSF/USGS, 2011) for a detailed
description of the modeling for marine
seismic source arrays for species
mitigation.
Table 1 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), serious injury, or mortality
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 (NMFS,
1995, 2000). The 180-dB and 190-dB
level shutdown criteria are applicable to
cetaceans and pinnipeds, respectively,
specified by us (NMFS, 1995, 2000).
Thus the Observatory used these
received sound levels to establish the
mitigation zones. We also assume that
marine mammals exposed to levels
exceeding 160 dB re: 1 mPa may
experience Level B harassment.
TABLE 1—MODELED DISTANCES TO WHICH SOUND LEVELS GREATER THAN OR EQUAL TO 160 AND 180 dB RE: 1 μPa
COULD BE RECEIVED DURING THE PROPOSED SURVEY OVER THE MID-ATLANTIC RIDGE IN THE NORTH ATLANTIC
OCEAN, DURING APRIL THROUGH JUNE, 2013
Source and volume
(in3)
Tow depth
(m)
Water depth
(m)
Predicted RMS
distances1 (m)
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160 dB
Single Bolt airgun (40 in3) .....................................................................................................
12
36-Airgun Array (6,600 in3) ....................................................................................................
12
> 1,000
100 to 1,000
> 1,000
100 to 1,000
388
582
6,908
10,362
180 dB
100
100
1,116
1,674
1 Diebold, J.B., M. Tolstoy, L. Doermann, S.L. Nooner, S.C. Webb, and T.J. Crone. 2010. R/V Marcus G. Langseth seismic source: Modeling
and calibration. Geochem. Geophys. Geosyst.
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Ocean Bottom Seismometers
The Observatory proposes to place 46
seismometers on the sea floor prior to
the initiation of the seismic survey.
Each seismometer is approximately 0.9
m (2.9 ft) high with a maximum
diameter of 97 centimeters (cm) (3.1 ft).
An anchor, made of a rolled steel bar
grate which measures approximately 7
by 91 by 91.5 cm (3 by 36 by 36 inches)
and weighs 45 kilograms (99 pounds)
would anchor the seismometer to the
seafloor.
After the Observatory completes the
proposed seismic survey, an acoustic
signal would trigger the release of each
of the 46 seismometers from the ocean
floor. The LANGSETH’s acoustic release
transponder, located on the vessel,
communicates with the seismometer at
a frequency of 9 to13 kilohertz (kHz).
The maximum source level of the
release signal is 242 dB re: 1 mPa with
an 8-millisecond pulse length. The
received signal activates the
seismometer’s double burn-wire release
assembly which then releases the
seismometer from the anchor. The
seismometer then floats to the ocean
surface for retrieval by the LANGSETH.
The steel grate anchors from each of the
seismometers would remain on the
seafloor.
The LANGSETH crew would deploy
the seismometers one-by-one from the
stern of the vessel while onboard
protected species observers will alert
them to the presence of marine
mammals and recommend ceasing
deploying or recovering the
seismometers to avoid potential
entanglement with marine mammal.
Thus, entanglement of marine mammals
is highly unlikely.
Although placement of the
seismometers is dispersed over
approximately1,500 square km (km2)
(579 square mi (mi2) of seafloor habitat
and may disturb benthic invertebrates,
we and the Observatory expect these
impacts to be localized and short-term
because of natural sedimentation
processes and the natural sinking of the
anchors from their own weight resulting
in no long-term habitat impacts. Also,
the deep water habitat potentially
affected by the placement of the
seismometers is not designated as a
marine protected area.
Multibeam Echosounder
The LANGSETH would operate a
Kongsberg EM 122 multibeam
echosounder concurrently during airgun
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operations to map characteristics of the
ocean floor. The hull-mounted
echosounder emits brief pulses of sound
(also called a ping) (10.5 to 13.0 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 crosstrack angular extent of about 150°, with
2-ms gaps between the pulses for
successive sectors.
Sub-Bottom Profiler
The LANGSETH would 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 27ß
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
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. We also expect these
disturbances to result in a temporary
modification in behavior and/or lowlevel physiological effects (Level B
PO 00000
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Fmt 4703
Sfmt 4703
10141
harassment) 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 Proposed Specified
Activity
Twenty-eight marine mammal species
under our jurisdiction may occur in the
proposed survey area, including seven
mysticetes (baleen whales), and 21
odontocetes (toothed cetaceans) during
April through May, 2013. Six of these
species are listed as endangered under
the Endangered Species Act of 1973
(ESA; 16 U.S.C. 1531 et seq.), including:
the blue (Balaenoptera musculus), fin
(Balaenoptera physalus), humpback
(Megaptera novaeangliae), north
Atlantic right (Eubalaena glacialis), sei
(Balaenoptera borealis), and sperm
(Physeter macrocephalus) whales.
Based on the best available data, the
Observatory does not expect to
encounter the following species because
of these species rare and/or extralimital
occurrence in the survey area. They
include the: Atlantic white-sided
dolphin (Lagenorhynchus acutus),
white-beaked dolphin (Lagenorhynchus
albirostris), harbor porpoise (Phocoena
phocoena), Clymene dolphin (Stenella
clymene), Fraser’s dolphin
(Lagenodelphis hosei), spinner dolphin
(Stenella longirostris), melon-headed
whale (Peponocephala electra), Atlantic
humpback dolphin (Souza teuszii),
long-beaked common dolphin
(Delphinus capensis), and any pinniped
species. Accordingly, we did not
consider these species in greater detail
and the proposed authorization would
only address requested take
authorizations for the 28 species.
Of these 28 species, the most common
marine mammals in the survey area
would be the: short-beaked common
dolphin (Delphinus delphis), striped
dolphin (Stenella coeruleoalba), and
short-finned pilot whale (Globicephala
macrorhynchus).
Table 2 presents information on the
abundance, distribution, and
conservation status of the marine
mammals that may occur in the
proposed survey area during April
through June, 2013.
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TABLE 2—ABUNDANCE ESTIMATES, MEAN DENSITY, AND ESA STATUS OF MARINE MAMMALS THAT MAY OCCUR IN THE
PROPOSED SEISMIC SURVEY AREA OVER THE MID-ATLANTIC RIDGE IN THE NORTH ATLANTIC OCEAN, DURING APRIL
THROUGH JUNE, 2013.
[See text and Table 2 in the Observatory’s application for further details]
Abundance in the
N. Atlantic Ocean
Species
Mysticetes:
North Atlantic right whale .............................................................
Humpback whale ..........................................................................
Minke whale .................................................................................
Bryde’s whale ...............................................................................
Sei whale ......................................................................................
Fin whale ......................................................................................
Blue whale ....................................................................................
Odontocetes:
Sperm whale ................................................................................
Pygmy sperm whale .....................................................................
Dwarf sperm whale ......................................................................
Cuvier’s beaked whale .................................................................
Mesoplodon spp. ..........................................................................
True’s beaked whale ....................................................................
Gervais beaked whale ..................................................................
Sowerby’s beaked whale .............................................................
Blainville’s beaked whale .............................................................
Northern bottlenose whale ...........................................................
Rough-toothed dolphin .................................................................
Common bottlenose dolphin ........................................................
Pantropical spotted dolphin ..........................................................
Atlantic spotted dolphin ................................................................
Striped dolphin .............................................................................
Short-beaked common dolphin ....................................................
Risso’s dolphin .............................................................................
Pygmy killer whale .......................................................................
False killer whale ..........................................................................
Killer whale ...................................................................................
Long-finned pilot whale ................................................................
Short-finned pilot whale ................................................................
ESA a
Estimated
Density
(#/100 km 2) b
396 1 ...............................................................
11,570 2 ..........................................................
121,000 3 ........................................................
Not available ..................................................
12–13,000 4 ....................................................
24,887 5 ..........................................................
937 6 ...............................................................
EN
EN
NL
NL
EN
EN
EN
0
0
0
0.19
0.19
4.46
1.49
13,190 7 ..........................................................
395 1 ...............................................................
395 1 ...............................................................
3,513 1,8 ..........................................................
3,513 1,8 ..........................................................
3,513 1,8 ..........................................................
3,513 1,8 ..........................................................
3,513 1,8 ..........................................................
3,513 1,8 ..........................................................
40,000 9 ..........................................................
Not available ..................................................
81,588 10 .........................................................
4,439 1 ............................................................
50,978 1 ..........................................................
94,462 1 ..........................................................
120,741 4 ........................................................
20,479 4 ..........................................................
Not available ..................................................
Not available ..................................................
Not available ..................................................
12,619,1 780,000 11 ........................................
24,674,1 780,000 11 ........................................
EN
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
NL
3.71
0
0
0
7.04
7.04
7.04
7.04
7.04
0
0
8.35
0
20.03
185.50
379.52
3.83
0
1.17
0
0
120.96
a ESA
status codes: NL—not listed under the ESA; EN—Endangered; T—Threatened
Observatory used Waring et al., 2008 to calculate density from sightings, effort, mean group sizes, and values for f(0) for the southern
part of the survey area.
1 Western North Atlantic, in U.S. and southern Canadian waters (Waring et al., 2012)
2 Likely negatively biased (Stevick et al., 2003)
3 Central and Northeast Atlantic (IWC, 2012)
4 North Atlantic (Cattanach et al., 1993)
5 Central and Northeast Atlantic (Vıkingsson et al., 2009)
´
6 Central and Northeast Atlantic (Pike et al., 2009).
7 For the northeast Atlantic, Faroes-Iceland, and the U.S. east coast (Whitehead, 2002).
8 Ziphius and Mesoplodon spp. combined
9 Eastern North Atlantic (NAMMCO, 1995)
10 Offshore, Western North Atlantic (Waring et al., 2012)
11 Globicephala sp. combined, Central and Eastern North Atlantic (IWC, 2012)
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b The
Refer to Section 4 of the Observatory’s
application and Sections 3.6.3.4 and
3.7.3.4 of the 2011 PEIS (NSF/USGS,
2011) 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.
We have reviewed these data and
determined them to be the best available
scientific information for the purposes
of the proposed incidental harassment
authorization.
Potential Effects on Marine Mammals
Acoustic stimuli generated by the
operation of the airguns, which
introduce sound into the marine
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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
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unlikely that the proposed project
would result in any cases of temporary
or permanent hearing impairment, or
any significant non-auditory physical or
physiological effects. Based on the
available data and studies described
here, we expect some behavioral
disturbance, but we expect the
disturbance to be localized. We refer the
reader to a more comprehensive review
of these issues in the 2011 PEIS (NSF/
USGS, 2011).
Tolerance
Studies on marine mammals’
tolerance to sound in the natural
environment are relatively rare.
Richardson et al. (1995) defined
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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. 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
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
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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.
Marine mammals are thought to be
able to compensate for masking by
adjusting their acoustic behavior
through shifting call frequencies,
increasing call volume, and increasing
vocalization rates. For example, blue
whales are found to increase call rates
when exposed to noise from seismic
surveys in the St. Lawrence Estuary
(Dilorio and Clark, 2009). The North
Atlantic right whales exposed to high
shipping noise increased call frequency
(Parks et al., 2007), while some
humpback whales respond to lowfrequency active sonar playbacks by
increasing song length (Miller et al.,
2000).
In general, we expect that the masking
effects of seismic pulses would be
minor, given the normally intermittent
nature of seismic pulses.
Behavioral Disturbance
Marine mammals may behaviorally
react to sound when exposed to
anthropogenic noise. 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
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10143
(Richardson et al., 1995; Wartzok et al.,
2004; Southall et al., 2007; Weilgart,
2007). These behavioral reactions are
often shown as: Changing durations of
surfacing and dives, number of blows
per surfacing, or moving direction and/
or speed; reduced/increased vocal
activities; changing/cessation of certain
behavioral activities (such as socializing
or feeding); visible startle response or
aggressive behavior (such as tail/fluke
slapping or jaw clapping); avoidance of
areas where noise sources are located;
and/or flight responses (e.g., pinnipeds
flushing into the water from haul-outs
or rookeries). 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).
The biological significance of many of
these behavioral disturbances is difficult
to predict, especially if the detected
disturbances appear minor. However,
the consequences of behavioral
modification could be expected to be
biologically significant if the change
affects growth, survival, and/or
reproduction. Some of these significant
behavioral modifications include:
• Change in diving/surfacing patterns
(such as those thought to be causing
beaked whale stranding due to exposure
to military mid-frequency tactical
sonar);
• Habitat abandonment due to loss of
desirable acoustic environment; and
• Cessation of feeding or social
interaction.
The onset of behavioral disturbance
from anthropogenic noise depends on
both external factors (characteristics of
noise sources and their paths) and the
receiving animals (hearing, motivation,
experience, demography) and is also
difficult to predict (Richardson et al.,
1995; Southall et al., 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
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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 and
small toothed whales, but for many
species there are no data on responses
to marine seismic surveys.
Baleen Whales—Baleen whales
generally tend to avoid operating
airguns, but avoidance radii are quite
variable (reviewed in Richardson et al.,
1995). Whales are often reported to
show no overt reactions to pulses from
large arrays of airguns at distances
beyond a few kilometers, even though
the airgun pulses remain well above
ambient noise levels out to much longer
distances. However, 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
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the responses of humpback whales off
western Australia to a full-scale seismic
survey with a 16-airgun array (2,678-in3)
and to a single, 20-in3 airgun with
source level of 227 dB re: 1 mPa (p-p).
In the 1998 study, the researchers
documented that avoidance reactions
began at five to eight km (3.1 to 4.9 mi)
from the array, and that those reactions
kept most pods approximately three to
four km (1.9 to 2.5 mi) from the
operating seismic boat. In the 2000
study, McCauley et al. noted localized
displacement during migration of four
to five km (2.5 to 3.1 mi) by traveling
pods and seven to 12 km (4.3 to 7.5 mi)
by more sensitive resting pods of cowcalf pairs. Avoidance distances with
respect to the single airgun were smaller
but consistent with the results from the
full array in terms of the received sound
levels. The mean received level for
initial avoidance of an approaching
airgun was 140 dB re: 1 mPa for
humpback pods containing females, and
at the mean closest point of approach
distance, the received level was 143 dB
re: 1 mPa. The initial avoidance response
generally occurred at distances of five to
eight km (3.1 to 4.9 mi) from the airgun
array and two km (1.2 mi) from the
single airgun. However, some individual
humpback whales, especially males,
approached within distances of 100 to
400 m (328 to 1,312 ft), where the
maximum received level was 179 dB re:
1 mPa.
Data collected by observers during
several seismic surveys in the northwest
Atlantic Ocean showed that sighting
rates of humpback whales were
significantly greater during non-seismic
periods compared with periods when a
full array was operating (Moulton and
Holst, 2010). In addition, humpback
whales were more likely to swim away
and less likely to swim towards a vessel
during seismic versus non-seismic
periods (Moulton and Holst, 2010).
Humpback whales on their summer
feeding grounds in southeast 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. However, Moulton and
Holst (2010) reported that humpback
whales monitored during seismic
surveys in the northwest Atlantic had
lower sighting rates and were most often
seen swimming away from the vessel
during seismic periods compared with
periods when airguns were silent.
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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).
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).
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 (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) observed
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localized avoidance by fin whales
during seismic airgun events in the
western Mediterranean Sea and adjacent
Atlantic waters from 2006–2009 and
reported that singing fin whales moved
away from an operating airgun array for
a time period that extended beyond the
duration of the airgun activity.
Ship-based monitoring studies of
baleen whales (including blue, fin, sei,
minke, and whales) in the northwest
Atlantic found that overall, this group
had lower sighting rates during seismic
versus non-seismic periods (Moulton
and Holst, 2010). Baleen whales as a
group were also seen significantly
farther from the vessel during seismic
compared with non-seismic periods,
and they were more often seen to be
swimming away from the operating
seismic vessel (Moulton and Holst,
2010). Blue and minke whales were
initially sighted significantly farther
from the vessel during seismic
operations compared to non-seismic
periods; the same trend was observed
for fin whales (Moulton and Holst,
2010). Minke whales were most often
observed to be swimming away from the
vessel when seismic operations were
underway (Moulton and Holst, 2010).
Data on short-term reactions by
cetaceans to impulsive noises are not
necessarily indicative of long-term or
biologically significant effects. It is not
known whether impulsive sounds affect
reproductive rate or distribution and
habitat use in subsequent days or years.
However, gray whales have continued to
migrate annually along the west coast of
North America with substantial
increases in the population over recent
years, despite intermittent seismic
exploration (and much ship traffic) in
that area for decades (Appendix A in
Malme et al., 1984; Richardson et al.,
1995; Allen and Angliss, 2011). The
western Pacific gray whale population
did not 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). The history of
coexistence between seismic surveys
and baleen whales suggests that brief
exposures to sound pulses from any
single seismic survey are unlikely to
result in prolonged effects.
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
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baleen whale/seismic pulse work
summarized earlier in this notice.
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.
Captive bottlenose dolphins (Tursiops
truncatus) and beluga whales
(Delphinapterus leucas) 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),
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10145
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. However, controlled
exposure experiments in the Gulf of
Mexico indicate that foraging behavior
was altered upon exposure to airgun
sound (Jochens et al., 2008; Miller et al.,
2009; Tyack, 2009).
There are almost no specific data on
the behavioral reactions of beaked
whales to seismic surveys. However,
some northern bottlenose whales
(Hyperoodon ampullatus) remained in
the general area and continued to
produce high-frequency clicks when
exposed to sound pulses from distant
seismic surveys (Gosselin and Lawson,
2004; Laurinolli and Cochrane, 2005;
Simard et al., 2005). Most beaked
whales tend to avoid approaching
vessels of other types (e.g., Wursig et al.,
1998). They may also dive for an
extended period when approached by a
vessel (e.g., Kasuya, 1986), although it is
uncertain how much longer such dives
may be as compared to dives by
undisturbed beaked whales, which also
are often quite long (Baird et al., 2006;
Tyack et al., 2006). Based on a single
observation, Aguilar-Soto et al. (2006)
suggested that foraging efficiency of
Cuvier’s beaked whales (Ziphius
cavirostris) may be reduced by close
approach of vessels. In any event, it is
likely that most beaked whales would
also show strong avoidance of an
approaching seismic vessel, although
this has not been documented
explicitly. In fact, Moulton and Holst
(2010) reported 15 sightings of beaked
whales during seismic studies in the
northwest Atlantic; seven of those
sightings were made at times when at
least one airgun was operating. There
was little evidence to indicate that
beaked whale behavior was affected by
airgun operations; sighting rates and
distances were similar during seismic
and non-seismic periods (Moulton and
Holst, 2010).
There are increasing indications that
some beaked whales tend to strand
when naval exercises involving midfrequency sonar operation are underway
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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 types of 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. However, other data
suggest that some odontocete species,
including harbor porpoises, may be
more responsive than might be expected
given their poor low-frequency hearing.
Reactions at longer distances may be
particularly likely when sound
propagation conditions are conducive to
transmission of the higher frequency
components of airgun sound to the
animals’ location (DeRuiter et al., 2006;
Goold and Coates, 2006; Tyack et al.,
2006; Potter et al., 2007).
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).
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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 1
(introduced earlier in this document)
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.
To avoid the potential for Level A
harassment, serious injury or mortality
we (NMFS 1995, 2000) concluded that
cetaceans should not be exposed to
pulsed underwater noise at received
levels exceeding 180 dB re: 1 mPa. We
do not consider the established 180
criterion to be the level above which
temporary threshold shift might occur.
Rather, it is a received level above
which, in the view of a panel of
bioacoustics specialists convened by us
before temporary threshold shift
measurements for marine mammals
started to become available, one could
not be certain that there would be no
injurious effects, auditory or otherwise,
to marine mammals. We also assume
that cetaceans exposed to levels
exceeding 160 dB re: 1 mPa may
experience Level B harassment.
For toothed whales, researchers have
derived temporary threshold shift
information for odontocetes from
studies on the bottlenose dolphin and
beluga. The experiments show that
exposure to a single impulse at a
received level of 207 kilopascals (or 30
psi, p-p), which is equivalent to 228 dB
re: 1 Pa (p-p), resulted in a 7 and 6 dB
temporary threshold shift in the beluga
whale at 0.4 and 30 kHz, respectively.
Thresholds returned to within 2 dB of
the pre-exposure level within four
minutes of the exposure (Finneran et al.,
2002). For the one harbor porpoise
tested, the received level of airgun
sound that elicited onset of temporary
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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, one could suspect that
received levels causing temporary
threshold shift onset may also be higher
in baleen whales (Southall et al., 2007).
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 (in sound
pressure level) would be approximately
181 to 186 dB re: 1 mPa (Southall et al.,
2007), or a series of pulses for which the
highest sound exposure level values are
a few decibels lower.
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
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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 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.
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 6 dB (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’’.
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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 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—Marine mammals close to
underwater detonations of high
explosives can be killed or severely
injured, and the auditory organs are
especially susceptible to injury (Ketten
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10147
et al., 1993; Ketten, 1995). However,
explosives are no longer used in marine
waters for commercial seismic surveys
or (with rare exceptions) for seismic
research. These methods have been
replaced entirely by airguns or related
non-explosive pulse generators. Airgun
pulses are less energetic and have
slower rise times, and there is no
specific evidence that they can cause
serious injury, death, or stranding even
in the case of large airgun arrays.
However, the association of
strandings of beaked whales with naval
exercises involving mid-frequency
active sonar and, in one case, the cooccurrence of a Lamont-Doherty’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).
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,
not seismic surveys (Cox et al., 2006;
Southall et al., 2007).
Seismic pulses and mid-frequency
sonar signals are quite different from
one another, 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
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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 correlation
between the potential effects of military
sonar on marine mammals and those
caused by seismic surveys using
airguns. 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 highintensity 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
Lamont-Doherty’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
approaching vessel before being
exposed to high sound levels; and
(2) Differences between the sound
sources operated by the LANGSETH 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
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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 would 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
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
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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 would 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
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
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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 would 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
LANGSETH 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 would 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
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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 would 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 would 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
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
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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
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
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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 would be audible to marine
mammals over a large distance, it is
unlikely that animals would 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.
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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
24.1 km/h (14.9 mph;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
seismic 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
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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.
Entanglement
Entanglement can occur if wildlife
becomes immobilized in survey lines,
cables, nets, or other equipment that is
moving through the water column. The
proposed seismic survey would require
towing approximately 8.0 km (4.9 mi) of
equipment and cables. This large of an
array carries the risk of entanglement for
marine mammals. Wildlife, especially
slow moving individuals, such as large
whales, have a low probability of
becoming entangled due to slow speed
of the survey vessel and onboard
monitoring efforts. The Observatory has
no recorded cases of entanglement of
marine mammals during the conduct of
over 8 years of seismic surveys covering
over 160,934 km (86,897.4 nmi) of
transect lines.
In May, 2011, there was one recorded
entanglement of an olive ridley sea
turtle (Lepidochelys olivacea) in the
LANGSETH’s barovanes after the
conclusion of a seismic survey off Costa
Rica. There have cases of baleen whales,
mostly gray whales (Heyning, 1990),
becoming entangled in fishing lines.
The probability for entanglement of
marine mammals is considered not
significant because of the vessel speed
and the monitoring efforts onboard the
survey vessel.
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
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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
would be temporarily elevated noise
levels and the associated direct effects
on marine mammals, previously
discussed in this notice. The next
section discusses the potential impacts
of anthropogenic sound sources on
common marine mammal prey in the
proposed survey area (i.e., fish and
invertebrates).
Anticipated Effects on Fish
One reason for the adoption of airguns
as the standard energy source for marine
seismic surveys is that, unlike
explosives, they have not been
associated with large-scale fish kills.
However, existing information on the
impacts of seismic surveys on marine
fish populations is limited. There are
three types of potential effects of
exposure to seismic surveys: (1)
Pathological, (2) physiological, and (3)
behavioral. Pathological effects involve
lethal and temporary or permanent sublethal injury. Physiological effects
involve temporary and permanent
primary and secondary stress responses,
such as changes in levels of enzymes
and proteins. Behavioral effects refer to
temporary and (if they occur) permanent
changes in exhibited behavior (e.g.,
startle and avoidance behavior). The
three categories are interrelated in
complex ways. For example, it is
possible that certain physiological and
behavioral changes could potentially
lead to an ultimate pathological effect
on individuals (i.e., mortality).
The specific received sound levels at
which permanent adverse effects to fish
potentially could occur are little studied
and largely unknown. Furthermore, the
available information on the impacts of
seismic surveys on marine fish is from
studies of individuals or portions of a
population; there have been no studies
at the population scale. The studies of
individual fish have often been on caged
fish that were exposed to airgun pulses
in situations not representative of an
actual seismic survey. Thus, available
information provides limited insight on
possible real-world effects at the ocean
or population scale.
Hastings and Popper (2005), Popper
(2009), and Popper and Hastings
(2009a,b) provided recent critical
reviews of the known effects of sound
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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 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. 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 the
Observatory, and 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
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10151
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 2 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).
An experiment of the effects of a
single 700 in3 airgun was conducted in
Lake Meade, Nevada (USGS, 1999). The
data were used in an Environmental
Assessment of the effects of a marine
reflection survey of the Lake Meade
fault system by the National Park
Service (Paulson et al., 1993, in USGS,
1999). They suspended the airgun 3.5 m
(11.5 ft) above a school of threadfin shad
in Lake Meade and fired three
successive times at a 30 second interval.
Neither surface inspection nor diver
observations of the water column and
bottom found any dead fish.
For a proposed seismic survey in
Southern California, USGS (1999)
conducted a review of the literature on
the effects of airguns on fish and
fisheries. They reported a 1991 study of
the Bay Area Fault system from the
continental shelf to the Sacramento
River, using a 10 airgun (5,828 in3)
array. Brezzina and Associates were
hired by USGS to monitor the effects of
the surveys, and concluded that airgun
operations were not responsible for the
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death of any of the fish carcasses
observed, and the airgun profiling did
not appear to alter the feeding behavior
of sea lions, seals, or pelicans observed
feeding during the seismic surveys.
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
of the sound stimulus.
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.
The Minerals Management Service
(MMS, 2005) assessed the effects of a
proposed seismic survey in Cook Inlet,
Alaska. The seismic survey proposed
using three vessels, each towing two,
four-airgun arrays ranging from 1,500 to
2,500 in3. The Minerals Management
Service noted that the impact to fish
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populations in the survey area and
adjacent waters would likely be very
low and temporary and also concluded
that seismic surveys may displace the
pelagic fishes from the area temporarily
when airguns are in use. However,
fishes displaced and avoiding the airgun
noise are likely to backfill the survey
area in minutes to hours after cessation
of seismic testing. Fishes not dispersing
from the airgun noise (e.g., demersal
species) may startle and move short
distances to avoid airgun emissions.
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 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).
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
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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 2011 PEIS (NSF/
USGS, 2011).
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.
Tenera Environmental (2011b)
reported that Norris and Mohl (1983,
summarized in Mariyasu et al., 2004)
observed lethal effects in squid (Loligo
vulgaris) at levels of 246 to 252 dB after
3 to 11 minutes.
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
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increased in severity with time,
suggesting that cephalopods are
particularly sensitive to low-frequency
sound. The received sound pressure
level was 157 ± 5 dB re: 1 mPa, with
peak levels at 175 dB re 1 mPa. As in the
McCauley et al. (2003) paper on sensory
hair cell damage in pink snapper as a
result of exposure to seismic sound, the
cephalopods were subjected to higher
sound levels than they would be under
natural conditions, and they were
unable to swim away from the sound
source.
Physiological Effects—Physiological
effects refer mainly to biochemical
responses by marine invertebrates to
acoustic stress. Such stress potentially
could affect invertebrate populations by
increasing mortality or reducing
reproductive success. Primary and
secondary stress responses (i.e., changes
in haemolymph levels of enzymes,
proteins, etc.) of crustaceans have been
noted several days or months after
exposure to seismic survey sounds
(Payne et al., 2007). It was noted
however, than no behavioral impacts
were exhibited by crustaceans (Christian
et al., 2003, 2004; DFO, 2004). The
periods necessary for these biochemical
changes to return to normal are variable
and depend on numerous aspects of the
biology of the species and of the sound
stimulus.
Behavioral Effects—There is
increasing interest in assessing the
possible direct and indirect effects of
seismic and other sounds on
invertebrate behavior, particularly in
relation to the consequences for
fisheries. Changes in behavior could
potentially affect such aspects as
reproductive success, distribution,
susceptibility to predation, and
catchability by fisheries. Studies
investigating the possible behavioral
effects of exposure to seismic survey
sound on crustaceans and cephalopods
have been conducted on both uncaged
and caged animals. In some cases,
invertebrates exhibited startle responses
(e.g., squid in McCauley et al., 2000a,b).
In other cases, no behavioral impacts
were noted (e.g., crustaceans in
Christian et al., 2003, 2004; DFO, 2004).
There have been anecdotal reports of
reduced catch rates of shrimp shortly
after exposure to seismic surveys;
however, other studies have not
observed any significant changes in
shrimp catch rate (Andriguetto-Filho et
al., 2005). Similarly, Parry and Gason
(2006) did not find any evidence that
lobster catch rates were affected by
seismic surveys. Any adverse effects on
crustacean and cephalopod behavior or
fisheries attributable to seismic survey
sound depend on the species in
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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 MMPA, 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 reviewed the
following source documents and have
incorporated a suite of proposed
mitigation measures into their project
description.
(1) Protocols used during previous
Foundation and Observatory-funded
seismic research cruises as approved by
us and detailed in the Foundation’s
2011 PEIS;
(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 have
proposed to implement the following
mitigation measures for marine
mammals:
(1) Vessel-based visual mitigation
monitoring;
(2) Proposed exclusion zones;
(3) Power down procedures;
(4) Shutdown procedures;
(5) Ramp-up procedures; and
(6) Speed and course alterations.
Vessel-Based Visual Mitigation
Monitoring
The Observatory would 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 would 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 would 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
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10153
LANGSETH would power down or
shutdown the airguns when marine
mammals are observed within or about
to enter a designated 180-dB exclusion
zone.
During seismic operations, at least
four protected species observers would
be aboard the LANGSETH. The
Observatory would appoint the
observers with our concurrence and
they would conduct observations during
ongoing daytime operations and
nighttime ramp-ups of the airgun array.
During the majority of seismic
operations, two observers would be on
duty from the observation tower to
monitor marine mammals near the
seismic vessel. Using two observers
would 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 would be on
watch during bathroom breaks and
mealtimes. Observers would be on duty
in shifts of no longer than four hours in
duration.
Two observers on the LANGSETH
would also be on visual watch during
all nighttime ramp-ups of the seismic
airguns. A third observer would 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 scheduled
two observers (visual) on duty from the
observation tower, and an observer
(acoustic) on the passive acoustic
monitoring system. Before the start of
the seismic survey, the Observatory
would 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 would be approximately
21.5 m (70.5 ft) above sea level, and the
observer would have a good view
around the entire vessel. During
daytime, the observers would 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 would be
available (ITT F500 Series Generation 3
binocular-image intensifier or
equivalent), when required. Laser rangefinding binoculars (Leica LRF 1200 laser
rangefinder or equivalent) would 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;
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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 would immediately power
down or shutdown the airguns. The
observer(s) would continue to maintain
watch to determine when the animal(s)
are outside the exclusion zone by visual
confirmation. Airgun operations would
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).
Proposed Exclusion Zones—The
Observatory would use safety radii to
designate exclusion zones and to
estimate take for marine mammals.
Table 1 (presented earlier in this
document) shows the distances at which
one would expect to receive three sound
levels (160- and 180-dB) from the 36airgun array and a single airgun. The
180-dB level shutdown criteria are
applicable to cetaceans 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
would 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 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 LANGSETH would
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. 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 would 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 would power-down
the airguns immediately. During a
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power down of the airgun array, the
crew would 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
1), the crew would shut down the single
airgun (see next section).
Resuming Airgun Operations After a
Power Down—Following a powerdown, the LANGSETH crew would not
resume full airgun activity until the
marine mammal has cleared the 180-dB
exclusion zone (see Table 1). The
observers would 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 LANGSETH crew would 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 would 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).
We estimate that the LANGSETH
would transit outside the original 180dB exclusion zone after an 8-minute
wait period. This period is based on the
180-dB exclusion zone for the 36-airgun
array towed at a depth of 12 m (39.4 ft)
in relation to the average speed of the
LANGSETH while operating the airguns
(8.5 km/h; 5.3 mph). Because the vessel
has transited 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
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
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this distance before resuming airgun
operations at full power.
Shutdown Procedures—The
LANGSETH crew would shutdown the
operating airgun(s) if a marine mammal
is seen within or approaching the
exclusion zone for the single airgun.
The crew would 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 would shutdown the
airgun(s) immediately in the unlikely
event that this species is observed,
regardless of the distance from the
vessel. The LANGSETH would only
begin ramp-up would only if the north
Pacific right whale has not been seen for
30 minutes.
Resuming Airgun Operations After a
Shutdown—Following a shutdown in
excess of eight minutes, the LANGSETH
crew would initiate a ramp-up with the
smallest airgun in the array (40-in3). The
crew would turn on additional airguns
in a sequence such that the source level
of the array would increase in steps not
exceeding 6 dB per five-minute period
over a total duration of approximately
30 minutes. During ramp-up, the
observers would monitor the exclusion
zone, and if he/she sights a marine
mammal, the LANGSETH crew would
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 would 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
would follow ramp-up procedures for a
shutdown described earlier and the
observers would monitor the full
exclusion zone and would 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 would 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 would not
ramp up the airgun array from a
complete shutdown at night or in thick
fog, because the outer part of the zone
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for that array would not be visible
during those conditions.
If one airgun has operated during a
power down period, ramp-up to full
power would be permissible at night or
in poor visibility, on the assumption
that marine mammals would be alerted
to the approaching seismic vessel by the
sounds from the single airgun and could
move away. The vessel’s crew would
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.
Ramp-Up Procedures—Ramp-up of an
airgun array provides a gradual increase
in sound levels, and involves a stepwise increase in the number and total
volume of airguns firing until the full
volume of the airgun array is achieved.
The purpose of a ramp-up is to ‘‘warn’’
marine mammals in the vicinity of the
airguns, and to provide the time for
them to leave the area and thus avoid
any potential injury or impairment of
their hearing abilities. The Observatory
would follow a ramp-up procedure
when the airgun array begins operating
after an 8 minute period without airgun
operations or when shut down has
exceeded that period. The Observatory
has used similar waiting periods
(approximately eight to 10 minutes)
during previous seismic surveys.
Ramp-up would begin with the
smallest airgun in the array (40 in3). The
crew would add airguns in a sequence
such that the source level of the array
would increase in steps not exceeding
six dB per five minute period over a
total duration of approximately 30 to 35
minutes. During ramp-up, the observers
would monitor the exclusion zone, and
if marine mammals are sighted, the
Observatory would implement a powerdown or shut-down as though the full
airgun array were operational.
If the complete exclusion zone has not
been visible for at least 30 minutes prior
to the start of operations in either
daylight or nighttime, the Observatory
would not commence the ramp-up
unless at least one airgun (40 in3 or
similar) has been operating during the
interruption of seismic survey
operations. Given these provisions, it is
likely that the crew would not ramp up
the airgun array from a complete shutdown at night or in thick fog, because
the outer part of the exclusion zone for
that array would not be visible during
those conditions. If one airgun has
operated during a power-down period,
ramp-up to full power would be
permissible at night or in poor visibility,
on the assumption that marine
mammals would be alerted to the
approaching seismic vessel by the
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sounds from the single airgun and could
move away. The Observatory would not
initiate a ramp-up of the airguns if a
marine mammal is sighted within or
near the applicable exclusion zones.
Speed and Course Alterations
If during seismic data collection, the
Observatory detects marine mammals
outside the exclusion zone and, based
on the animal’s position and direction
of travel, is likely to enter the exclusion
zone, the LANGSETH would change
speed and/or direction if this does not
compromise operational safety. Due to
the limited maneuverability of the
primary survey vessel, altering speed
and/or course can result in an extended
period of time to realign onto the
transect. However, if the animal(s)
appear likely to enter the exclusion
zone, the LANGSETH would undertake
further mitigation actions, including a
power down or shut down of the
airguns.
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.
Proposed Monitoring and Reporting
In order to issue an incidental take
authorization for an activity, section
101(a)(5)(D) of the MMPA 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
would 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
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10155
present project to supplement the
mitigation measures that require realtime monitoring, and to satisfy the
monitoring requirements of the
Incidental Harassment Authorization.
The Observatory understands that this
monitoring plan would be subject to
review by us, and that we may require
refinements to the plan. The
Observatory 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 is prepared to
discuss coordination of its monitoring
program with any other related work
that might be conducted by other groups
working insofar as it is practical and
desirable.
Vessel-Based Passive Acoustic
Monitoring
Passive acoustic monitoring would
complement the visual mitigation
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.
Passive acoustical monitoring can be
used in conjunction with visual
observations to improve detection,
identification, and localization of
cetaceans. The passive acoustic
monitoring would 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 would monitor
the system in real time so that he/she
can advise the visual observers if they
acoustic detect cetaceans.
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 would deploy the array from a
winch located on the back deck. A deck
cable would connect the tow cable to
the electronics unit in the main
computer lab where the acoustic station,
signal conditioning, and processing
system would be located. The acoustic
signals received by the hydrophones are
amplified, digitized, and then processed
by the Pamguard software. The system
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can detect marine mammal
vocalizations at frequencies up to 250
kHz.
One acoustic observer, an expert
bioacoustician with primary
responsibility for the passive acoustic
monitoring system would be aboard the
LANGSETH in addition to the four
visual observers. The acoustic observer
would 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 would 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
would be on shift for one to six hours
at a time. The other observers would
rotate as an acoustic observer, although
the expert acoustician would 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 would 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
would enter the information regarding
the call into a database. Data entry
would 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 would record data to
estimate the numbers of marine
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mammals exposed to various received
sound levels and to document apparent
disturbance reactions or lack thereof.
They would 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
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 would 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.
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Proposed Reporting
The Observatory would submit a
report to us and to the Foundation
within 90 days after the end of the
cruise. The report would describe the
operations that were conducted and
sightings of marine mammals and
turtles near the operations. The report
would provide full documentation of
methods, results, and interpretation
pertaining to all monitoring. The 90-day
report would summarize the dates and
locations of seismic operations, and all
marine mammal sightings (dates, times,
locations, activities, associated seismic
survey activities). The report would 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 not
permitted by the authorization (if
issued), such as an injury, 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. 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 MMPA
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
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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. 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 would 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
would 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, within 24 hours of
the discovery. The Observatory would
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 MMPA
defines ‘‘harassment’’ as: Any act of
pursuit, torment, or annoyance which (i)
has the potential to injure a marine
mammal or marine mammal stock in the
wild [Level A harassment]; or (ii) has
the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment].
We propose to authorize take by Level
B harassment for the proposed seismic
survey. Acoustic stimuli (i.e., increased
underwater sound) generated during the
operation of the seismic airgun array
may have the potential to result in the
behavioral disturbance of some marine
mammals. There is no evidence that
planned activities could result in
serious injury or mortality within the
specified geographic area for the
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17:21 Feb 12, 2013
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requested authorization. The required
mitigation and monitoring measures
would minimize any potential risk for
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
estimates are based on a consideration
of the number of marine mammals that
could be harassed by seismic operations
with the 36-airgun array during
approximately 5,572 km2 (2,151 mi2) of
transect lines on the Mid-Atlantic Ridge
in the north Atlantic Ocean, as depicted
in Figure 1 of the application.
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).
Density Information—The
Observatory based the density estimates
on information calculated from
sightings, effort, mean group sizes, and
values for f(0) for the southern part of
the survey area in Waring et al. (2008),
which extends from the Azores at
approximately 38° N to 53° N. The
allocated densities calculated for
undifferentiated ‘‘common/striped
dolphins’’ to common and striped
dolphins in proportion to the calculated
densities of the two species. The density
calculated for ‘‘unidentified dolphin’’
was allocated to bottlenose, Atlantic
spotted, and Risso’s dolphins, species
that could occur in the proposed survey
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10157
area based on their presence in the
Azores, in proportion to the number of
sightings in the OBIS database for those
species around the Azores. The density
calculated for ‘‘unidentified small
whale’’ was allocated to the false killer
whale, the one small whale species that
could occur in the proposed survey area
based on its presence in the Azores. The
four ‘‘long-finned/short-finned pilot
whales’’ sighted in the southern part of
the survey area by Waring et al. (2008)
were assumed to be short-finned pilot
whales based on OBIS sightings around
the Azores. The density calculated for
the one ‘‘sei/Bryde’s whale’’ sighting in
the southern part of the survey area was
allocated to sei and Bryde’s whales in
equal proportions. The authors’
calculated value of f(0) for the sei whale
was used for calculating densities of
Bryde’s, fin, and blue whales, and that
for ‘‘small Delphinidae’’ was used for
calculating densities of Mesoplodon
spp., dolphins, the false killer whale,
and the short-finned pilot whale.
Because the survey effort in the
southern stratum of Waring et al. (2008)
is limited (1,047 km; 650 mi), the survey
area is north of the proposed seismic
area (38–52° N versus 36–36.5° N), and
the survey was conducted during a
somewhat different season (June versus
April–May), there is some uncertainty
about the representativeness of the data
and the assumptions used in the
calculations.
Exposure Estimation—The
Observatory estimated 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 on one or more occasions by
considering the total marine area that
would be within the 160-dB radius
around the operating airgun array on at
least one occasion and the expected
density of marine mammals. The
number of possible exposures
(including repeat exposures of the same
individuals) can be estimated by
considering the total marine area that
would be within the 160-dB radius
around the operating airguns, excluding
areas of overlap. Some individuals may
be exposed multiple times since the
survey tracklines are spaced close
together, however, it is unlikely that a
particular animal would stay in the area
during the entire survey.
The number of different individuals
potentially exposed to received levels
greater than or equal to 160 re: 1 mPa
(rms) was calculated by multiplying:
(1) The expected species density (in
number/km2), times
(2) The anticipated area to be
ensonified to that level during airgun
operations (5,571 km2; (2,151 mi2).
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The Observatory’s estimates of
exposures to various sound levels
assume that the proposed surveys
would be carried out in full (i.e.,
approximately 20 days of seismic airgun
operations), however, the ensonified
areas calculated using the planned
number of line-kilometers have been
increased by 25 percent to accommodate
lines that may need to be repeated,
equipment testing, account for repeat
exposure, etc. As is typical during
offshore ship surveys, inclement
weather and equipment malfunctions
are likely to cause delays and may limit
the number of useful line-kilometers of
seismic operations that can be
undertaken.
TABLE 3—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 SEISMIC SURVEY OVER THE MID-ATLANTIC RIDGE IN THE
NORTH ATLANTIC OCEAN, DURING APRIL THROUGH JUNE, 2013
Species
Estimated number of
individuals exposed
to sound levels
≥160 dB re: 1 μPa1
Mysticetes:
North Atlantic right whale ...........................................................
Humpback whale ........................................................................
Minke whale ................................................................................
Bryde’s whale .............................................................................
Sei whale ....................................................................................
Fin whale ....................................................................................
Blue whale ..................................................................................
Odontocetes
Sperm whale ...............................................................................
Pygmy sperm whale ...................................................................
Dwarf sperm whale .....................................................................
Cuvier’s beaked whale ...............................................................
Mesoplodon spp. ........................................................................
True’s beaked whale ..................................................................
Gervais beaked whale ................................................................
Sowerby’s beaked whale ............................................................
Blainville’s beaked whale ...........................................................
Northern bottlenose whale .........................................................
Rough-toothed dolphin ...............................................................
Common bottlenose dolphin .......................................................
Pantropical spotted dolphin ........................................................
Atlantic spotted dolphin ..............................................................
Striped dolphin ............................................................................
Short-beaked common dolphin ...................................................
Risso’s dolphin ...........................................................................
Pygmy killer whale ......................................................................
False killer whale ........................................................................
Killer whale .................................................................................
Long-finned pilot whale ..............................................................
Short-finned pilot whale ..............................................................
0
0
0
1
1
25
8
..................................
21
0
0
0
..................................
..................................
39
..................................
..................................
0
0
47
0
112
1,034
2,115
21
0
7
0
0
674
Requested
or adjusted take
authorization 2
0
42
43
1
1
25
8
21
............................
0
0
47
............................
............................
39
............................
............................
44
0
47
0
112
1,034
2,115
21
0
7
45
0
674
Regional
population 3
Approx.
percent of
regional
population 3
0
0
0
N/A
13,000
24,887
937
........................
13,190
395
395
3,513
........................
........................
........................
........................
3,502
∼40,000
N/A
81,588
4,439
50,978
94,462
120,741
20,479
N/A
N/A
N/A
780,000
780,000
0
0
0
N/A
0.01
0.10
0.89
0.16
........................
0
0
0.2
........................
........................
1.12
........................
........................
0
0
0.06
0
0.22
1.09
1.75
0.10
0
N/A
0
0
0.09
N/A = Not Available.
1 Estimates are based on densities in Table 2 and an ensonified area of (5,571 km2; (2,151 mi2)
2 Requested or adjusted take includes a 25 percent contingency for repeated exposures due to the overlap of parallel survey tracks.
3 Regional population size estimates are from Table 2.
4 Requested take authorization increased to group size for species for which densities were not calculated but for which there were OBIS
sightings around the Azores.
mstockstill on DSK4VPTVN1PROD with NOTICES
Encouraging and Coordinating
Research
The Observatory would coordinate
the planned marine mammal monitoring
program associated with the seismic
survey on the Mid-Atlantic Ridge in the
north Atlantic 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
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18:10 Feb 12, 2013
Jkt 229001
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);
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(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 and based on the following
factors, 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.
They include:
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(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
(including power-downs and
shutdowns); and
(3) 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 behavioral
disturbance to occur during the conduct
of the survey activities.
Table 4 in this document outlines 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
survey would last no more than 20 days.
Additionally, the seismic survey would
be increasing sound levels in the marine
environment in a relatively small area
surrounding the vessel (compared to the
range of the animals), which is
constantly travelling over distances, and
some animals may only be exposed to
and harassed by sound for shorter less
than day.
Of the 28 marine mammal species
under our jurisdiction that are known to
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17:21 Feb 12, 2013
Jkt 229001
occur or likely to occur in the study
area, six of these species are listed as
endangered under the ESA, including:
The blue, fin, humpback, north Atlantic
right, sei, and sperm whales. These
species are also categorized as depleted
under the MMPA. With the exception of
the north Atlantic right whale, the
Observatory has requested authorized
take for these listed species.
As mentioned previously, we estimate
that 28 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 take numbers are small
(most estimates are less than or equal to
two percent) 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 Table 4 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 a proposed survey on the
Mid-Atlantic Ridge in the north Atlantic
Ocean in international waters, from
April 2013 through June 2013, may
result, at worst, in a modification in
behavior and/or low-level physiological
effects (Level B harassment) of certain
species of marine mammals.
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 and sporadic
duration of the research activities, have
led us to preliminary determine that this
action would 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
planned research activities would result
in the incidental take of small numbers
of marine mammals, by Level B
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10159
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
would 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 (on the Mid-Atlantic
Ridge in the north Atlantic Ocean in
international waters) 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 Atlantic right, sei, and sperm
whales. The Observatory did not request
take of endangered north Atlantic 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. Both
agencies would conclude the formal
section 7 consultation (with a single
Biological Opinion for the Foundation’s
Division of Ocean Sciences and NMFS’
Office of Protected Resources, Permits
and Conservation Division federal
actions) 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
mandatory Terms and Conditions of the
Opinion’s Incidental Take Statement
which would incorporate the mitigation
and monitoring requirements included
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in the Incidental Harassment
Authorization.
Commission and its Committee of
Scientific Advisors.
National Environmental Policy Act
(NEPA)
Dated: February 6, 2013.
Matthew J. Brookhart,
Acting Director, Office of Protected Resources,
National Marine Fisheries Service.
To meet our NEPA requirements for
the issuance of an IHA to the
Observatory, we intend to prepare an
Environmental Assessment (EA) titled
‘‘Issuance of an Incidental Harassment
Authorization to the Lamont-Doherty
Earth Observatory to Take Marine
Mammals by Harassment Incidental to a
Marine Geophysical on the Mid-Atlantic
Ridge in the north Atlantic Ocean, from
April 2013 through June 2013.’’ This EA
would incorporate as appropriate the
Foundation’s Environmental Analysis
Pursuant To Executive Order 12114
(NSF, 2010) titled, ‘‘Marine geophysical
survey by the R/V MARCUS G. Langseth
on the mid-Atlantic Ridge, April–May
2013,’’ by reference pursuant to 40 CFR
1502.21 and NOAA Administrative
Order (NAO) 216–6 § 5.09(d). Prior to
making a final decision on the IHA
application, we would decide whether
or not to issue a Finding of No
Significant Impact (FONSI).
The Foundation’s environmental
analysis is available for review at the
addresses set forth earlier in this notice.
This notice and the documents it
references provide all relevant
environmental information related to
our proposal to issue the IHA. We invite
the public’s comment and will consider
any comments related to environmental
effects related to the proposed issuance
of the IHA submitted in response to this
as we conduct and finalize our NEPA
analysis.
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 on the Mid-Atlantic
Ridge in the north Atlantic Ocean from
April 2013, through June 2013, 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.
mstockstill on DSK4VPTVN1PROD with NOTICES
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
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17:21 Feb 12, 2013
Jkt 229001
[FR Doc. 2013–03321 Filed 2–12–13; 8:45 am]
BILLING CODE 3510–22–P
DELAWARE RIVER BASIN
COMMISSION
Notice of Commission Meeting and
Public Hearing
Notice is hereby given that the
Delaware River Basin Commission will
hold a public hearing on Tuesday,
March 5, 2013. A business meeting will
be held the following day on
Wednesday, March 6, 2013. Both the
hearing and business meeting are open
to the public and will be held at the
Commission’s office building located at
25 State Police Drive, West Trenton,
New Jersey.
Public Hearing. The public hearing on
March 5, 2013 will run from 1:00 p.m.
until approximately 4:00 p.m. The list of
projects scheduled for hearing, with
descriptions, is currently available in a
long form of this notice posted on the
Commission’s Web site, www.drbc.net.
Draft dockets and resolutions for
hearing items will be posted on the Web
site approximately ten days prior to the
hearing date. Because hearings on
particular projects may be postponed to
allow additional time for the
commission’s review, interested parties
are advised to check the Web site
periodically prior to the hearing date.
Postponements, if any, will be duly
noted there.
Public Meeting. The business meeting
on March 6, 2013 will begin at 12:15
p.m. and will include the following
items: adoption of the Minutes of the
Commission’s December 5, 2012
business meeting, announcements of
upcoming meetings and events, a report
on hydrologic conditions, reports by the
Executive Director and the
Commission’s General Counsel,
consideration of items for which a
hearing has been completed, and a
public dialogue session. The
Commissioners also may consider
action on matters not subject to a public
hearing.
There will be no opportunity for
additional public comments at the
March 6 business meeting on items for
which a hearing was completed on
March 5 or a previous date. Commission
consideration on March 6 of items for
which the public hearing is closed may
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result in either approval of the docket or
resolution as proposed, approval with
changes, denial, or deferral. When the
commissioners defer an action, they
may announce an additional period for
written comment on the item, with or
without an additional hearing date, or
they may take additional time to
consider the input they have already
received without requesting further
public input. Any deferred items will be
considered for action at a public
meeting of the commission on a future
date.
Advance sign-up for oral comment.
Individuals who wish to comment for
the record at the public hearing on
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ext. 224.
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E:\FR\FM\13FEN1.SGM
13FEN1
Agencies
[Federal Register Volume 78, Number 30 (Wednesday, February 13, 2013)]
[Notices]
[Pages 10137-10160]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-03321]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XC238
Takes of Marine Mammals Incidental to Specified Activities;
Marine Geophysical Survey on the Mid-Atlantic Ridge in the Atlantic
Ocean, April 2013, Through June 2013
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 (Observatory), in collaboration with the National Science
Foundation (Foundation), for an Incidental Harassment Authorization to
take marine mammals, by harassment, incidental to conducting a marine
geophysical (seismic) survey on the Mid-Atlantic Ridge in the north
Atlantic Ocean in international waters, from April 2013 through May
2013. Per the Marine Mammal Protection Act, we are requesting comments
on our proposal to issue an Incidental Harassment Authorization to the
Observatory and the Foundation to incidentally harass by Level B
harassment only, 28 species of marine mammals during the 20-day seismic
survey.
DATES: Comments and information must be received no later than March
15, 2013.
ADDRESSES: Comments on the application should be addressed to P.
Michael Payne, Chief, Permits and Conservation Division, Office of
Protected Resources, National Marine Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910-3225. The mailbox address for
providing email comments is ITP.Cody@noaa.gov. Please include 0648-
XC238 in the subject line. We are not responsible for email comments
sent to other addresses other than the one provided here. Comments sent
via email to ITP.Cody@noaa.gov, 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, 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 following associated documents are also available at the same
internet address:
The Foundation's draft environmental analysis titled, ``Marine
geophysical survey by the R/V MARCUS G. LANGSETH on the mid-Atlantic
Ridge, April-May 2013,'' for their federal action of funding the
Observatory's seismic survey. LGL Ltd., Environmental Research
Associates (LGL), prepared this analysis on behalf of the Foundation
pursuant to Executive Order 12114: Environmental Effects Abroad of
Major Federal Actions. The Foundation's environmental analysis
evaluates the effects of the proposed seismic survey on the human
environment including impacts to marine mammals. We will prepare a
separate National Environmental Policy Act (NEPA: 42 U.S.C. 4321 et
seq.) analysis to evaluate the environmental effects related to the
scope of our federal action which is the proposed issuance of an
incidental take authorization to the Observatory and the Foundation. We
plan to incorporate the Foundation's environmental analysis, in whole
or part, by reference, into our NEPA document as that analysis provides
a detailed description of the planned survey and its anticipated
effects on marine mammals. This notice and the referenced document
present detailed information on the scope of our federal action under
NEPA (i.e., potential impacts to marine mammals from
[[Page 10138]]
issuing the proposed IHA including measures for mitigation, and
monitoring) and we will consider comments submitted in response to this
notice as we prepare our NEPA analysis.
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, 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, after notice of a proposed authorization to the
public for review and public comment: (1) We make certain findings; and
(2) the taking is limited to harassment.
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 taking. 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 MMPA established an expedited process
by which citizens of the United States can apply for an authorization
to incidentally take small numbers of marine mammals by harassment.
Section 101(a)(5)(D) of the MMPA establishes a 45-day time limit for
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
MMPA defines ``harassment'' as: any act of pursuit, torment, or
annoyance which (i) has the potential to injure a marine mammal or
marine mammal stock in the wild [Level A harassment]; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment].
Summary of Request
We received an application from the Observatory on December 7,
2012, requesting that we issue an Incidental Harassment Authorization
(Authorization) for the take, by Level B harassment only, of small
numbers of marine mammals incidental to conducting a marine seismic
survey in the north Atlantic Ocean in international waters from April
8, 2013, through May 13, 2013. We received a revised application from
the Observatory on December 23, 2012 and January 17, 2013, which
reflected updates to the mitigation safety zones, incidental take
requests for marine mammals, and information on marine protected areas.
Upon receipt of additional information, we determined the application
complete and adequate on January 18, 2013.
Project Purpose--The Observatory plans to conduct a two-dimensional
(2-D) seismic survey on the Mid-Atlantic Ridge in the north Atlantic
Ocean. Specifically, the proposed survey would image the Rainbow massif
to determine the characteristics of the magma body that supplies heat
to the Rainbow hydrothermal field; determine the distribution of the
different rock types that form the Rainbow massif; document large- and
small-scale faults in the vicinity and investigate their role in
controlling hydrothermal fluid discharge.
Vessel--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 (seismometers) to
conduct the seismic survey. In addition to the operations of the
seismic airgun array and hydrophone streamer, and the seismometers, the
Observatory intends to operate a multibeam echosounder and a sub-bottom
profiler continuously throughout the proposed survey.
Marine Mammal Take--Acoustic stimuli (i.e., increased underwater
sound) generated during the operation of the seismic airgun arrays, may
have the potential to cause behavioral disturbance for marine mammals
in the survey area. This is the principal means of marine mammal take
associated with these activities and the Observatory requested an
authorization to take 28 species of marine mammals by Level B
harassment.
In the Observatory's application, they did not request
authorization to take marine mammals by Level A Harassment because
their environmental analyses estimate that marine mammals would not be
exposed to levels of sound likely to result in Level A harassment (we
refer the reader to Appendix B of the Foundation's NEPA document
titled, ``2011 Final Programmatic Environmental Impact Statement/
Overseas Environmental Impact Statement (2011 PEIS) for Marine Seismic
Research funded by the National Science Foundation or Conducted by the
U.S. Geological Survey,'' (NSF/USGS, 2011) at https://www.nsf.gov/geo/oce/envcomp/usgs-nsf-marine-seismic-research/nsf-usgs-final-eis-oeis-with-appendices.pdf for details). Consequently, the Observatory's
request for take by Level A harassment is zero animals for any species.
We do not expect that the use of the multibeam echosounder, the
sub-bottom profiler, or the ocean bottom seismometer would 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 during seismic acquisition activities because the vessel moves
at a relatively slow speed (approximately 8.3 kilometers per hour (km/
h); 5.2 miles per hour (mph); 4.5 knots (kts)), for a relatively short
period of time (approximately 20 operational days). It is likely that
any marine mammal would be able to avoid the vessel during seismic
acquisition activities. The Observatory has no recorded cases of a
vessel strike with a marine mammal during the conduct of over eight
years of seismic surveys covering over 160,934 km (86,897.4 nmi) of
transect lines.
Description of the Proposed Specified Activities
Survey Details
The Observatory's proposed seismic survey on the Mid-Atlantic Ridge
in the north Atlantic Ocean would commence
[[Page 10139]]
on April 8, 2013, and end on May 13, 2013. The LANGSETH would depart
from St. George's, Bermuda, on April 8, 2013, and transit to the
proposed survey area in international waters approximately 300 km
(186.4 miles (mi)) offshore of Pico and Faial Islands in the Azores. At
the conclusion of the proposed survey activities, the LANGSETH would
arrive in Ponta Delgada, Azores on May 13, 2012. The proposed study
area would encompass an area on the Mid-Atlantic Ridge bounded by the
following coordinates: Approximately 35.5 to 36.5[deg] North by 33.5 to
34.5[deg] West.
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 that is effective from April 8, 2013, to June 24, 2013.
Typically, 2-D surveys 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 the survey, the LANGSETH would deploy
an 36-airgun array as an energy source, an 8-kilometer (km)-long (3.7
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.
The LANGSETH would transect approximately 2,582 km (1.6 mi) of
transect lines which are spaced 1 to 2 meters (m) (3.2 to 6.6 feet
(ft)) apart from one another (see Figure 1 in the Observatory's
application). As the LANGSETH tows the airgun array along the transect
lines, the hydrophone streamer would receive the returning acoustic
signals and transfer the data to the vessel's onboard processing
system. The seismometers also record and store the returning signals
for later analysis. The LANGSETH would retrieve the seismometers at the
conclusion of the survey.
The proposed study (e.g., equipment testing, startup, line changes,
repeat coverage of any areas, and equipment recovery) would require
approximately 20 days. At the proposed survey area, the LANGSETH would
conduct seismic acquisition activities in a grid pattern using the
seismometers as a receiver over a total of approximately 1,680 km
(1,044 mi) of survey lines and would also conduct seismic acquisition
activities in multichannel seismic (MCS) mode using the 8-km (3.7 mi)
streamer as the receiver over a total of approximately 900 km (559 mi).
The seismic lines are over water depths of approximately 900 to 3,000 m
(2,952 ft to 1.9 mi). Approximately 2,565 km (1,594 mi) of the survey
effort would occur in depths greater than 1,000 m (3,280 ft). The
remaining effort (17 km; 10.5 mi) would occur in water depths of 100 to
1,000 m (328 to 3,280 ft).
The proposed data acquisition would include approximately 480 hours
of airgun operations (i.e., 20 days over 24 hours), with airgun
discharges occurring on either a 3.25 minute interval with the
seismometers or a 16-second interval for the MCS seismic portion. The
Observatory would conduct all planned seismic activities with on-board
assistance by the scientists who have proposed the study, Drs. J.P.
Canales and R. Sohn of Woods Hole Oceanographic Institution and Dr. R.
Dunn of the University of Hawaii. The vessel is self-contained and the
crew would live aboard the vessel for the entire cruise.
Vessel Specifications
R/V LANGSETH
The LANGSETH, owned by the Foundation and operated by the
Observatory, 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. Its 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 cruising speed of the vessel outside of seismic
operations is 18.5 km/h (11.5 mph; 10 kts).
The LANGSETH would 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) would watch for marine mammals
before and during the proposed seismic acquisition operations. When
stationed on the observation platform, the observer's eye level would
be approximately 21.5 m (71 ft) above sea level providing the observer
an unobstructed view around the entire vessel.
Acoustic Source Specifications
Seismic Airguns
The LANGSETH would deploy an 36-airgun array, with a total volume
of approximately 6,600 cubic inches (in\3\). The airguns are a mixture
of Bolt 1500LL and Bolt 1900LLX airguns ranging in size from 40 to 360
in\3\, with a firing pressure of 1,900 pounds per square inch. The
dominant frequency components range from zero to 188 Hertz (Hz). The
array configuration consists of four identical linear strings, with 10
airguns on each string; the first and last airguns would be spaced 16 m
(52 ft) apart. Of the 10 airguns, nine would fire simultaneously while
the tenth airgun would serve as a spare in case of failure of one of
the other airguns. The LANGSETH would distribute the array across an
area of approximately 24 x 16 m (78.7 x 52.5 ft) and would tow the
array approximately 30 m (98.4 ft) behind the vessel at a tow depth of
12 m (39.4 ft) (see Figure 2-11, page 2-25 in the Foundation's 2011
PEIS) (NSF/USGS, 2011). During firing, the airguns would 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. 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 [micro]Pa, and
the units for sound pressure levels are dB re: 1 [mu]Pa. Sound pressure
level (in decibels (dB)) = 20 log (pressure/reference pressure).
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
[[Page 10140]]
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 on the LANGSETH is
236 to 265 dB re: 1 [micro]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 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.
Appendix H of the Foundation's PEIS (NSF/USGS, 2011) provides a
detailed description of the modeling for marine seismic source arrays
for species mitigation. 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. We refer the
reader to the Observatory's authorization application and the
Foundation's PEIS for additional information.
Predicted Sound Levels for the Airguns
The Observatory has developed a model (Diebold et al., 2010) that
predicts received sound levels as a function of distance from the
airguns for the 36-airgun array and the single 40-in\3\ airgun. Their
modeling approach uses ray tracing (i.e., a graphical representation of
the effects of refracting sound waves) for the direct wave traveling
from the array to the receiver and its associated source ghost
(reflection at the air-water interface in the vicinity of the array),
in a constant-velocity half-space (infinite homogeneous ocean layer,
unbounded by a seafloor).
Additionally, Tolstoy et al., (2009) reported results for
propagation measurements of pulses from the LANGSETH's 36-airgun 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 their algorithm for acoustic
modeling (Diebold et al., 2010) to calculate the exclusion zones for
the 36-airgun array and the single airgun. These values designate
mitigation zones used during power downs or shutdowns for marine
mammals. The Observatory uses the mitigation zones to estimate take
(described in greater detail in Chapter 7 of the application) for
marine mammals.
Comparison of the Tolstoy et al. (2009) calibration study with the
Observatory's model (Diebold et al., 2010) for the LANGSETH's 36-airgun
array indicated that the Observatory's model represents the actual
received levels, within the first few kilometers and the locations of
the predicted exclusions zones. Thus, the comparison of results from
the Tolstoy et al. (2009) calibration study with the Observatory's
model (Diebold et al., 2010) at short ranges for the same array tow
depth are in good agreement (see Figures 12 and 14 in Diebold et al.,
2010). As a consequence, isopleths falling within this domain can be
predicted reliably by the Observatory's model.
In contrast, for actual received levels at longer distances, the
Observatory found that their model (Diebold et al., 2010) was a more
robust tool for estimating mitigation radii in deep water as it did not
overestimate the received sound levels at a given distance. To estimate
mitigation radii in intermediate water depths, the Observatory applied
a correction factor (multiplication) of 1.5 to the deep water
mitigation radii. We refer the reader to Appendix H of the Foundation's
PEIS (NSF/USGS, 2011) for a detailed description of the modeling for
marine seismic source arrays for species mitigation.
Table 1 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), serious injury,
or mortality 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 (NMFS, 1995,
2000). The 180-dB and 190-dB level shutdown criteria are applicable to
cetaceans and pinnipeds, respectively, specified by us (NMFS, 1995,
2000). Thus the Observatory used these received sound levels to
establish the mitigation zones. We also assume that marine mammals
exposed to levels exceeding 160 dB re: 1 [micro]Pa may experience Level
B harassment.
Table 1--Modeled Distances to Which Sound Levels Greater Than or Equal to 160 and 180 dB re: 1 [micro]Pa Could
Be Received During the Proposed Survey Over the Mid-Atlantic Ridge in the North Atlantic Ocean, During April
Through June, 2013
----------------------------------------------------------------------------------------------------------------
Predicted RMS
Tow depth Water depth distances\1\ (m)
Source and volume (in\3\) (m) (m) ---------------------
160 dB 180 dB
----------------------------------------------------------------------------------------------------------------
Single Bolt airgun (40 in\3\)................................. 12 > 1,000 388 100
100 to 1,000 582 100
36-Airgun Array (6,600 in\3\)................................. 12 > 1,000 6,908 1,116
100 to 1,000 10,362 1,674
----------------------------------------------------------------------------------------------------------------
\1\ Diebold, J.B., M. Tolstoy, L. Doermann, S.L. Nooner, S.C. Webb, and T.J. Crone. 2010. R/V Marcus G. Langseth
seismic source: Modeling and calibration. Geochem. Geophys. Geosyst.
[[Page 10141]]
Ocean Bottom Seismometers
The Observatory proposes to place 46 seismometers on the sea floor
prior to the initiation of the seismic survey. Each seismometer is
approximately 0.9 m (2.9 ft) high with a maximum diameter of 97
centimeters (cm) (3.1 ft). An anchor, made of a rolled steel bar grate
which measures approximately 7 by 91 by 91.5 cm (3 by 36 by 36 inches)
and weighs 45 kilograms (99 pounds) would anchor the seismometer to the
seafloor.
After the Observatory completes the proposed seismic survey, an
acoustic signal would trigger the release of each of the 46
seismometers from the ocean floor. The LANGSETH's acoustic release
transponder, located on the vessel, communicates with the seismometer
at a frequency of 9 to13 kilohertz (kHz). The maximum source level of
the release signal is 242 dB re: 1 [mu]Pa with an 8-millisecond pulse
length. The received signal activates the seismometer's double burn-
wire release assembly which then releases the seismometer from the
anchor. The seismometer then floats to the ocean surface for retrieval
by the LANGSETH. The steel grate anchors from each of the seismometers
would remain on the seafloor.
The LANGSETH crew would deploy the seismometers one-by-one from the
stern of the vessel while onboard protected species observers will
alert them to the presence of marine mammals and recommend ceasing
deploying or recovering the seismometers to avoid potential
entanglement with marine mammal. Thus, entanglement of marine mammals
is highly unlikely.
Although placement of the seismometers is dispersed over
approximately1,500 square km (km\2\) (579 square mi (mi\2\) of seafloor
habitat and may disturb benthic invertebrates, we and the Observatory
expect these impacts to be localized and short-term because of natural
sedimentation processes and the natural sinking of the anchors from
their own weight resulting in no long-term habitat impacts. Also, the
deep water habitat potentially affected by the placement of the
seismometers is not designated as a marine protected area.
Multibeam Echosounder
The LANGSETH would 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 13.0 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 would 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[ordm] cone.
The power output is 10 kilowatts (kW), but the actual maximum radiated
power is three kilowatts or 222 dB re: 1 [micro]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 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. We also expect these disturbances to result in
a temporary modification in behavior and/or low-level physiological
effects (Level B harassment) 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 Proposed Specified
Activity
Twenty-eight marine mammal species under our jurisdiction may occur
in the proposed survey area, including seven mysticetes (baleen
whales), and 21 odontocetes (toothed cetaceans) during April through
May, 2013. Six of these species are listed as endangered under the
Endangered Species Act of 1973 (ESA; 16 U.S.C. 1531 et seq.),
including: the blue (Balaenoptera musculus), fin (Balaenoptera
physalus), humpback (Megaptera novaeangliae), north Atlantic right
(Eubalaena glacialis), sei (Balaenoptera borealis), and sperm (Physeter
macrocephalus) whales.
Based on the best available data, the Observatory does not expect
to encounter the following species because of these species rare and/or
extralimital occurrence in the survey area. They include the: Atlantic
white-sided dolphin (Lagenorhynchus acutus), white-beaked dolphin
(Lagenorhynchus albirostris), harbor porpoise (Phocoena phocoena),
Clymene dolphin (Stenella clymene), Fraser's dolphin (Lagenodelphis
hosei), spinner dolphin (Stenella longirostris), melon-headed whale
(Peponocephala electra), Atlantic humpback dolphin (Souza teuszii),
long-beaked common dolphin (Delphinus capensis), and any pinniped
species. Accordingly, we did not consider these species in greater
detail and the proposed authorization would only address requested take
authorizations for the 28 species.
Of these 28 species, the most common marine mammals in the survey
area would be the: short-beaked common dolphin (Delphinus delphis),
striped dolphin (Stenella coeruleoalba), and short-finned pilot whale
(Globicephala macrorhynchus).
Table 2 presents information on the abundance, distribution, and
conservation status of the marine mammals that may occur in the
proposed survey area during April through June, 2013.
[[Page 10142]]
Table 2--Abundance Estimates, Mean Density, and ESA Status of Marine
Mammals That May Occur in the Proposed Seismic Survey Area Over the Mid-
Atlantic Ridge in the North Atlantic Ocean, During April Through June,
2013.
[See text and Table 2 in the Observatory's application for further
details]
------------------------------------------------------------------------
Estimated
Abundance in ESA Density (/100 km \2\)
Atlantic Ocean \b\
------------------------------------------------------------------------
Mysticetes:
North Atlantic right 396 \1\........ EN 0
whale.
Humpback whale.......... 11,570 \2\..... EN 0
Minke whale............. 121,000 \3\.... NL 0
Bryde's whale........... Not available.. NL 0.19
Sei whale............... 12-13,000 \4\.. EN 0.19
Fin whale............... 24,887 \5\..... EN 4.46
Blue whale.............. 937 \6\........ EN 1.49
Odontocetes:
Sperm whale............. 13,190 \7\..... EN 3.71
Pygmy sperm whale....... 395 \1\........ NL 0
Dwarf sperm whale....... 395 \1\........ NL 0
Cuvier's beaked whale... 3,513 \1,8\.... NL 0
Mesoplodon spp.......... 3,513 \1,8\.... NL 7.04
True's beaked whale..... 3,513 \1,8\.... NL 7.04
Gervais beaked whale.... 3,513 \1,8\.... NL 7.04
Sowerby's beaked whale.. 3,513 \1,8\.... NL 7.04
Blainville's beaked 3,513 \1,8\.... NL 7.04
whale.
Northern bottlenose 40,000 \9\..... NL 0
whale.
Rough-toothed dolphin... Not available.. NL 0
Common bottlenose 81,588 \10\.... NL 8.35
dolphin.
Pantropical spotted 4,439 \1\...... NL 0
dolphin.
Atlantic spotted dolphin 50,978 \1\..... NL 20.03
Striped dolphin......... 94,462 \1\..... NL 185.50
Short-beaked common 120,741 \4\.... NL 379.52
dolphin.
Risso's dolphin......... 20,479 \4\..... NL 3.83
Pygmy killer whale...... Not available.. NL 0
False killer whale...... Not available.. NL 1.17
Killer whale............ Not available.. NL 0
Long-finned pilot whale. 12,619,\1\ NL 0
780,000 \11\.
Short-finned pilot whale 24,674,\1\ NL 120.96
780,000 \11\.
------------------------------------------------------------------------
\a\ ESA status codes: NL--not listed under the ESA; EN--Endangered; T--
Threatened
\b\ The Observatory used Waring et al., 2008 to calculate density from
sightings, effort, mean group sizes, and values for f(0) for the
southern part of the survey area.
\1\ Western North Atlantic, in U.S. and southern Canadian waters (Waring
et al., 2012)
\2\ Likely negatively biased (Stevick et al., 2003)
\3\ Central and Northeast Atlantic (IWC, 2012)
\4\ North Atlantic (Cattanach et al., 1993)
\5\ Central and Northeast Atlantic (V[iacute]kingsson et al., 2009)
\6\ Central and Northeast Atlantic (Pike et al., 2009).
\7\ For the northeast Atlantic, Faroes-Iceland, and the U.S. east coast
(Whitehead, 2002).
\8\ Ziphius and Mesoplodon spp. combined
\9\ Eastern North Atlantic (NAMMCO, 1995)
\10\ Offshore, Western North Atlantic (Waring et al., 2012)
\11\ Globicephala sp. combined, Central and Eastern North Atlantic (IWC,
2012)
Refer to Section 4 of the Observatory's application and Sections
3.6.3.4 and 3.7.3.4 of the 2011 PEIS (NSF/USGS, 2011) 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. We have reviewed these data
and determined them to be the best available scientific information for
the purposes of the proposed incidental harassment authorization.
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 here, we expect some
behavioral disturbance, but we expect the disturbance to be localized.
We refer the reader to a more comprehensive review of these issues in
the 2011 PEIS (NSF/USGS, 2011).
Tolerance
Studies on marine mammals' tolerance to sound in the natural
environment are relatively rare. Richardson et al. (1995) defined
[[Page 10143]]
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. 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
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.
Marine mammals are thought to be able to compensate for masking by
adjusting their acoustic behavior through shifting call frequencies,
increasing call volume, and increasing vocalization rates. For example,
blue whales are found to increase call rates when exposed to noise from
seismic surveys in the St. Lawrence Estuary (Dilorio and Clark, 2009).
The North Atlantic right whales exposed to high shipping noise
increased call frequency (Parks et al., 2007), while some humpback
whales respond to low-frequency active sonar playbacks by increasing
song length (Miller et al., 2000).
In general, we expect that the masking effects of seismic pulses
would be minor, given the normally intermittent nature of seismic
pulses.
Behavioral Disturbance
Marine mammals may behaviorally react to sound when exposed to
anthropogenic noise. 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). These behavioral
reactions are often shown as: Changing durations of surfacing and
dives, number of blows per surfacing, or moving direction and/or speed;
reduced/increased vocal activities; changing/cessation of certain
behavioral activities (such as socializing or feeding); visible startle
response or aggressive behavior (such as tail/fluke slapping or jaw
clapping); avoidance of areas where noise sources are located; and/or
flight responses (e.g., pinnipeds flushing into the water from haul-
outs or rookeries). 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).
The biological significance of many of these behavioral
disturbances is difficult to predict, especially if the detected
disturbances appear minor. However, the consequences of behavioral
modification could be expected to be biologically significant if the
change affects growth, survival, and/or reproduction. Some of these
significant behavioral modifications include:
Change in diving/surfacing patterns (such as those thought
to be causing beaked whale stranding due to exposure to military mid-
frequency tactical sonar);
Habitat abandonment due to loss of desirable acoustic
environment; and
Cessation of feeding or social interaction.
The onset of behavioral disturbance from anthropogenic noise
depends on both external factors (characteristics of noise sources and
their paths) and the receiving animals (hearing, motivation,
experience, demography) and is also difficult to predict (Richardson et
al., 1995; Southall et al., 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
[[Page 10144]]
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 and small toothed
whales, but for many species there are no data on responses to marine
seismic surveys.
Baleen Whales--Baleen whales generally tend to avoid operating
airguns, but avoidance radii are quite variable (reviewed in Richardson
et al., 1995). Whales are often reported to show no overt reactions to
pulses from large arrays of airguns at distances beyond a few
kilometers, even though the airgun pulses remain well above ambient
noise levels out to much longer distances. However, 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 [micro]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 [micro]Pa.
Researchers have studied the responses of humpback whales to
seismic surveys during migration, feeding during the summer months,
breeding while offshore from Angola, and wintering offshore from
Brazil. McCauley et al. (1998, 2000a) studied the responses of humpback
whales off western Australia to a full-scale seismic survey with a 16-
airgun array (2,678-in\3\) and to a single, 20-in\3\ airgun with source
level of 227 dB re: 1 [micro]Pa (p-p). In the 1998 study, the
researchers documented that avoidance reactions began at five to eight
km (3.1 to 4.9 mi) from the array, and that those reactions kept most
pods approximately three to four km (1.9 to 2.5 mi) from the operating
seismic boat. In the 2000 study, McCauley et al. noted localized
displacement during migration of four to five km (2.5 to 3.1 mi) by
traveling pods and seven to 12 km (4.3 to 7.5 mi) by more sensitive
resting pods of cow-calf pairs. Avoidance distances with respect to the
single airgun were smaller but consistent with the results from the
full array in terms of the received sound levels. The mean received
level for initial avoidance of an approaching airgun was 140 dB re: 1
[micro]Pa for humpback pods containing females, and at the mean closest
point of approach distance, the received level was 143 dB re: 1
[micro]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 [micro]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 southeast 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. However, Moulton and Holst (2010)
reported that humpback whales monitored during seismic surveys in the
northwest Atlantic had lower sighting rates and were most often seen
swimming away from the vessel during seismic periods compared with
periods when airguns were silent.
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).
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 [micro]Pa. Those findings
were generally consistent with the results of experiments conducted on
larger numbers of gray whales that were migrating along the California
coast (Malme et al., 1984; Malme and Miles, 1985), and western Pacific
gray whales feeding off Sakhalin Island, Russia (Wursig et al., 1999;
Gailey et al., 2007; Johnson et al., 2007; Yazvenko et al., 2007a,b),
along with data on gray whales off British Columbia (Bain and Williams,
2006).
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 (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)
observed
[[Page 10145]]
localized avoidance by fin whales during seismic airgun events in the
western Mediterranean Sea and adjacent Atlantic waters from 2006-2009
and reported that singing fin whales moved away from an operating
airgun array for a time period that extended beyond the duration of the
airgun activity.
Ship-based monitoring studies of baleen whales (including blue,
fin, sei, minke, and whales) in the northwest Atlantic found that
overall, this group had lower sighting rates during seismic versus non-
seismic periods (Moulton and Holst, 2010). Baleen whales as a group
were also seen significantly farther from the vessel during seismic
compared with non-seismic periods, and they were more often seen to be
swimming away from the operating seismic vessel (Moulton and Holst,
2010). Blue and minke whales were initially sighted significantly
farther from the vessel during seismic operations compared to non-
seismic periods; the same trend was observed for fin whales (Moulton
and Holst, 2010). Minke whales were most often observed to be swimming
away from the vessel when seismic operations were underway (Moulton and
Holst, 2010).
Data on short-term reactions by cetaceans to impulsive noises are
not necessarily indicative of long-term or biologically significant
effects. It is not known whether impulsive sounds affect reproductive
rate or distribution and habitat use in subsequent days or years.
However, gray whales have continued to migrate annually along the west
coast of North America with substantial increases in the population
over recent years, despite intermittent seismic exploration (and much
ship traffic) in that area for decades (Appendix A in Malme et al.,
1984; Richardson et al., 1995; Allen and Angliss, 2011). The western
Pacific gray whale population did not 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). The
history of coexistence between seismic surveys and baleen whales
suggests that brief exposures to sound pulses from any single seismic
survey are unlikely to result in prolonged effects.
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 this notice. 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.
Captive bottlenose dolphins (Tursiops truncatus) and beluga whales
(Delphinapterus leucas) 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. However, controlled exposure experiments in the Gulf
of Mexico indicate that foraging behavior was altered upon exposure to
airgun sound (Jochens et al., 2008; Miller et al., 2009; Tyack, 2009).
There are almost no specific data on the behavioral reactions of
beaked whales to seismic surveys. However, some northern bottlenose
whales (Hyperoodon ampullatus) remained in the general area and
continued to produce high-frequency clicks when exposed to sound pulses
from distant seismic surveys (Gosselin and Lawson, 2004; Laurinolli and
Cochrane, 2005; Simard et al., 2005). Most beaked whales tend to avoid
approaching vessels of other types (e.g., Wursig et al., 1998). They
may also dive for an extended period when approached by a vessel (e.g.,
Kasuya, 1986), although it is uncertain how much longer such dives may
be as compared to dives by undisturbed beaked whales, which also are
often quite long (Baird et al., 2006; Tyack et al., 2006). Based on a
single observation, Aguilar-Soto et al. (2006) suggested that foraging
efficiency of Cuvier's beaked whales (Ziphius cavirostris) may be
reduced by close approach of vessels. In any event, it is likely that
most beaked whales would also show strong avoidance of an approaching
seismic vessel, although this has not been documented explicitly. In
fact, Moulton and Holst (2010) reported 15 sightings of beaked whales
during seismic studies in the northwest Atlantic; seven of those
sightings were made at times when at least one airgun was operating.
There was little evidence to indicate that beaked whale behavior was
affected by airgun operations; sighting rates and distances were
similar during seismic and non-seismic periods (Moulton and Holst,
2010).
There are increasing indications that some beaked whales tend to
strand when naval exercises involving mid-frequency sonar operation are
underway
[[Page 10146]]
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 types of 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. However, other data suggest that some odontocete species,
including harbor porpoises, may be more responsive than might be
expected given their poor low-frequency hearing. Reactions at longer
distances may be particularly likely when sound propagation conditions
are conducive to transmission of the higher frequency components of
airgun sound to the animals' location (DeRuiter et al., 2006; Goold and
Coates, 2006; Tyack et al., 2006; Potter et al., 2007).
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 1 (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.
To avoid the potential for Level A harassment, serious injury or
mortality we (NMFS 1995, 2000) concluded that cetaceans should not be
exposed to pulsed underwater noise at received levels exceeding 180 dB
re: 1 [mu]Pa. We do not consider the established 180 criterion to be
the level above which temporary threshold shift might occur. Rather, it
is a received level above which, in the view of a panel of bioacoustics
specialists convened by us before temporary threshold shift
measurements for marine mammals started to become available, one could
not be certain that there would be no injurious effects, auditory or
otherwise, to marine mammals. We also assume that cetaceans exposed to
levels exceeding 160 dB re: 1 [mu]Pa may experience Level B harassment.
For toothed whales, researchers have derived temporary threshold
shift information for odontocetes from studies on the bottlenose
dolphin and beluga. The experiments show that exposure to a single
impulse at a received level of 207 kilopascals (or 30 psi, p-p), which
is equivalent to 228 dB re: 1 Pa (p-p), resulted in a 7 and 6 dB
temporary threshold shift in the beluga whale at 0.4 and 30 kHz,
respectively. Thresholds returned to within 2 dB of the pre-exposure
level within four minutes of the exposure (Finneran et al., 2002). 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, one could suspect that received
levels causing temporary threshold shift onset may also be higher in
baleen whales (Southall et al., 2007).
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 (in sound
pressure level) would be approximately 181 to 186 dB re: 1 [mu]Pa
(Southall et al., 2007), or a series of pulses for which the highest
sound exposure level values are a few decibels lower.
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
[[Page 10147]]
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 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. 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 6 dB (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--Marine mammals close
to underwater detonations of high explosives can be killed or severely
injured, and the auditory organs are especially susceptible to injury
(Ketten et al., 1993; Ketten, 1995). However, explosives are no longer
used in marine waters for commercial seismic surveys or (with rare
exceptions) for seismic research. These methods have been replaced
entirely by airguns or related non-explosive pulse generators. Airgun
pulses are less energetic and have slower rise times, and there is no
specific evidence that they can cause serious injury, death, or
stranding even in the case of large airgun arrays.
However, the association of strandings of beaked whales with naval
exercises involving mid-frequency active sonar and, in one case, the
co-occurrence of a Lamont-Doherty'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).
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, not seismic surveys (Cox et al., 2006; Southall et
al., 2007).
Seismic pulses and mid-frequency sonar signals are quite different
from one another, 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
[[Page 10148]]
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 correlation between the potential effects of
military sonar on marine mammals and those caused by seismic surveys
using airguns. 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 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 Lamont-Doherty'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 LANGSETH
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 would 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 would 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 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 [mu]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
[[Page 10149]]
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 would 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 LANGSETH 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 would 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 would 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 would 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
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 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
[[Page 10150]]
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 would be audible to
marine mammals over a large distance, it is unlikely that animals would
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 24.1 km/h (14.9 mph;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 seismic 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.
Entanglement
Entanglement can occur if wildlife becomes immobilized in survey
lines, cables, nets, or other equipment that is moving through the
water column. The proposed seismic survey would require towing
approximately 8.0 km (4.9 mi) of equipment and cables. This large of an
array carries the risk of entanglement for marine mammals. Wildlife,
especially slow moving individuals, such as large whales, have a low
probability of becoming entangled due to slow speed of the survey
vessel and onboard monitoring efforts. The Observatory has no recorded
cases of entanglement of marine mammals during the conduct of over 8
years of seismic surveys covering over 160,934 km (86,897.4 nmi) of
transect lines.
In May, 2011, there was one recorded entanglement of an olive
ridley sea turtle (Lepidochelys olivacea) in the LANGSETH's barovanes
after the conclusion of a seismic survey off Costa Rica. There have
cases of baleen whales, mostly gray whales (Heyning, 1990), becoming
entangled in fishing lines. The probability for entanglement of marine
mammals is considered not significant because of the vessel speed and
the monitoring efforts onboard the survey vessel.
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
[[Page 10151]]
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 would be
temporarily elevated noise levels and the associated direct effects on
marine mammals, previously discussed in this notice. The next section
discusses the potential impacts of anthropogenic sound sources on
common marine mammal prey in the proposed survey area (i.e., fish and
invertebrates).
Anticipated Effects on Fish
One reason for the adoption of airguns as the standard energy
source for marine seismic surveys is that, unlike explosives, they have
not been associated with large-scale fish kills. However, existing
information on the impacts of seismic surveys on marine fish
populations is limited. 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 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. 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 the Observatory, and 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 2 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).
An experiment of the effects of a single 700 in\3\ airgun was
conducted in Lake Meade, Nevada (USGS, 1999). The data were used in an
Environmental Assessment of the effects of a marine reflection survey
of the Lake Meade fault system by the National Park Service (Paulson et
al., 1993, in USGS, 1999). They suspended the airgun 3.5 m (11.5 ft)
above a school of threadfin shad in Lake Meade and fired three
successive times at a 30 second interval. Neither surface inspection
nor diver observations of the water column and bottom found any dead
fish.
For a proposed seismic survey in Southern California, USGS (1999)
conducted a review of the literature on the effects of airguns on fish
and fisheries. They reported a 1991 study of the Bay Area Fault system
from the continental shelf to the Sacramento River, using a 10 airgun
(5,828 in\3\) array. Brezzina and Associates were hired by USGS to
monitor the effects of the surveys, and concluded that airgun
operations were not responsible for the
[[Page 10152]]
death of any of the fish carcasses observed, and the airgun profiling
did not appear to alter the feeding behavior of sea lions, seals, or
pelicans observed feeding during the seismic surveys.
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 of the sound
stimulus.
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.
The Minerals Management Service (MMS, 2005) assessed the effects of
a proposed seismic survey in Cook Inlet, Alaska. The seismic survey
proposed using three vessels, each towing two, four-airgun arrays
ranging from 1,500 to 2,500 in\3\. The Minerals Management Service
noted that the impact to fish populations in the survey area and
adjacent waters would likely be very low and temporary and also
concluded that seismic surveys may displace the pelagic fishes from the
area temporarily when airguns are in use. However, fishes displaced and
avoiding the airgun noise are likely to backfill the survey area in
minutes to hours after cessation of seismic testing. Fishes not
dispersing from the airgun noise (e.g., demersal species) may startle
and move short distances to avoid airgun emissions.
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 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).
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 2011 PEIS (NSF/USGS,
2011).
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.
Tenera Environmental (2011b) reported that Norris and Mohl (1983,
summarized in Mariyasu et al., 2004) observed lethal effects in squid
(Loligo vulgaris) at levels of 246 to 252 dB after 3 to 11 minutes.
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
[[Page 10153]]
increased in severity with time, suggesting that cephalopods are
particularly sensitive to low-frequency sound. The received sound
pressure level was 157 5 dB re: 1 [micro]Pa, with peak
levels at 175 dB re 1 [micro]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). It was
noted however, than no behavioral impacts were exhibited by crustaceans
(Christian et al., 2003, 2004; DFO, 2004). The periods necessary for
these biochemical changes to return to normal are variable and depend
on numerous aspects of the biology of the species and of the sound
stimulus.
Behavioral Effects--There is increasing interest in assessing the
possible direct and indirect effects of seismic and other sounds on
invertebrate behavior, particularly in relation to the consequences for
fisheries. Changes in behavior could potentially affect such aspects as
reproductive success, distribution, susceptibility to predation, and
catchability by fisheries. Studies investigating the possible
behavioral effects of exposure to seismic survey sound on crustaceans
and cephalopods have been conducted on both uncaged and caged animals.
In some cases, invertebrates exhibited startle responses (e.g., squid
in McCauley et al., 2000a,b). In other cases, no behavioral impacts
were noted (e.g., crustaceans in Christian et al., 2003, 2004; DFO,
2004). There have been anecdotal reports of reduced catch rates of
shrimp shortly after exposure to seismic surveys; however, other
studies have not observed any significant changes in shrimp catch rate
(Andriguetto-Filho et al., 2005). Similarly, Parry and Gason (2006) did
not find any evidence that lobster catch rates were affected by seismic
surveys. Any adverse effects on crustacean and cephalopod behavior or
fisheries attributable to seismic survey sound depend on the species in
question and the nature of the fishery (season, duration, fishing
method).
Proposed Mitigation
In order to issue an incidental take authorization under section
101(a)(5)(D) of the MMPA, 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 reviewed the following source documents and
have incorporated a suite of proposed mitigation measures into their
project description.
(1) Protocols used during previous Foundation and Observatory-
funded seismic research cruises as approved by us and detailed in the
Foundation's 2011 PEIS;
(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
have proposed to implement the following mitigation measures for marine
mammals:
(1) Vessel-based visual mitigation monitoring;
(2) Proposed exclusion zones;
(3) Power down procedures;
(4) Shutdown procedures;
(5) Ramp-up procedures; and
(6) Speed and course alterations.
Vessel-Based Visual Mitigation Monitoring
The Observatory would 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 would
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 would 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 would power down or shutdown the airguns
when marine mammals are observed within or about to enter a designated
180-dB exclusion zone.
During seismic operations, at least four protected species
observers would be aboard the LANGSETH. The Observatory would appoint
the observers with our concurrence and they would conduct observations
during ongoing daytime operations and nighttime ramp-ups of the airgun
array. During the majority of seismic operations, two observers would
be on duty from the observation tower to monitor marine mammals near
the seismic vessel. Using two observers would 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 would be on watch
during bathroom breaks and mealtimes. Observers would be on duty in
shifts of no longer than four hours in duration.
Two observers on the LANGSETH would also be on visual watch during
all nighttime ramp-ups of the seismic airguns. A third observer would
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 scheduled two observers
(visual) on duty from the observation tower, and an observer (acoustic)
on the passive acoustic monitoring system. Before the start of the
seismic survey, the Observatory would 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 would be
approximately 21.5 m (70.5 ft) above sea level, and the observer would
have a good view around the entire vessel. During daytime, the
observers would 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
would 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) would 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;
[[Page 10154]]
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 would immediately power down or
shutdown the airguns. The observer(s) would continue to maintain watch
to determine when the animal(s) are outside the exclusion zone by
visual confirmation. Airgun operations would 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).
Proposed Exclusion Zones--The Observatory would use safety radii to
designate exclusion zones and to estimate take for marine mammals.
Table 1 (presented earlier in this document) shows the distances at
which one would expect to receive three sound levels (160- and 180-dB)
from the 36-airgun array and a single airgun. The 180-dB level shutdown
criteria are applicable to cetaceans 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 would 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 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 LANGSETH would 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. 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 would 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 would power-down the airguns
immediately. During a power down of the airgun array, the crew would
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 1), the crew would shut down
the single airgun (see next section).
Resuming Airgun Operations After a Power Down--Following a power-
down, the LANGSETH crew would not resume full airgun activity until the
marine mammal has cleared the 180-dB exclusion zone (see Table 1). The
observers would 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 LANGSETH crew would 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 would 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).
We estimate that the LANGSETH would transit 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 towed at a
depth of 12 m (39.4 ft) in relation to the average speed of the
LANGSETH while operating the airguns (8.5 km/h; 5.3 mph). Because the
vessel has transited 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 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.
Shutdown Procedures--The LANGSETH crew would shutdown the operating
airgun(s) if a marine mammal is seen within or approaching the
exclusion zone for the single airgun. The crew would 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 would shutdown the airgun(s) immediately in the
unlikely event that this species is observed, regardless of the
distance from the vessel. The LANGSETH would only begin ramp-up would
only if the north Pacific right whale has not been seen for 30 minutes.
Resuming Airgun Operations After a Shutdown--Following a shutdown
in excess of eight minutes, the LANGSETH crew would initiate a ramp-up
with the smallest airgun in the array (40-in\3\). The crew would turn
on additional airguns in a sequence such that the source level of the
array would increase in steps not exceeding 6 dB per five-minute period
over a total duration of approximately 30 minutes. During ramp-up, the
observers would monitor the exclusion zone, and if he/she sights a
marine mammal, the LANGSETH crew would 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 would 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 would follow
ramp-up procedures for a shutdown described earlier and the observers
would monitor the full exclusion zone and would 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 would 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 would not ramp up the airgun array
from a complete shutdown at night or in thick fog, because the outer
part of the zone
[[Page 10155]]
for that array would not be visible during those conditions.
If one airgun has operated during a power down period, ramp-up to
full power would be permissible at night or in poor visibility, on the
assumption that marine mammals would be alerted to the approaching
seismic vessel by the sounds from the single airgun and could move
away. The vessel's crew would 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.
Ramp-Up Procedures--Ramp-up of an airgun array provides a gradual
increase in sound levels, and involves a step-wise increase in the
number and total volume of airguns firing until the full volume of the
airgun array is achieved. The purpose of a ramp-up is to ``warn''
marine mammals in the vicinity of the airguns, and to provide the time
for them to leave the area and thus avoid any potential injury or
impairment of their hearing abilities. The Observatory would follow a
ramp-up procedure when the airgun array begins operating after an 8
minute period without airgun operations or when shut down has exceeded
that period. The Observatory has used similar waiting periods
(approximately eight to 10 minutes) during previous seismic surveys.
Ramp-up would begin with the smallest airgun in the array (40
in\3\). The crew would add airguns in a sequence such that the source
level of the array would increase in steps not exceeding six dB per
five minute period over a total duration of approximately 30 to 35
minutes. During ramp-up, the observers would monitor the exclusion
zone, and if marine mammals are sighted, the Observatory would
implement a power-down or shut-down as though the full airgun array
were operational.
If the complete exclusion zone has not been visible for at least 30
minutes prior to the start of operations in either daylight or
nighttime, the Observatory would not commence the 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 crew would not ramp up the airgun array from a
complete shut-down at night or in thick fog, because the outer part of
the exclusion zone for that array would not be visible during those
conditions. If one airgun has operated during a power-down period,
ramp-up to full power would be permissible at night or in poor
visibility, on the assumption that marine mammals would be alerted to
the approaching seismic vessel by the sounds from the single airgun and
could move away. The Observatory would not initiate a ramp-up of the
airguns if a marine mammal is sighted within or near the applicable
exclusion zones.
Speed and Course Alterations
If during seismic data collection, the Observatory detects marine
mammals outside the exclusion zone and, based on the animal's position
and direction of travel, is likely to enter the exclusion zone, the
LANGSETH would change speed and/or direction if this does not
compromise operational safety. Due to the limited maneuverability of
the primary survey vessel, altering speed and/or course can result in
an extended period of time to realign onto the transect. However, if
the animal(s) appear likely to enter the exclusion zone, the LANGSETH
would undertake further mitigation actions, including a power down or
shut down of the airguns.
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.
Proposed Monitoring and Reporting
In order to issue an incidental take authorization for an activity,
section 101(a)(5)(D) of the MMPA 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
would 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 to supplement the mitigation measures that require
real-time monitoring, and to satisfy the monitoring requirements of the
Incidental Harassment Authorization. The Observatory understands that
this monitoring plan would be subject to review by us, and that we may
require refinements to the plan. The Observatory 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 is prepared to discuss coordination of
its monitoring program with any other related work that might be
conducted by other groups working insofar as it is practical and
desirable.
Vessel-Based Passive Acoustic Monitoring
Passive acoustic monitoring would complement the visual mitigation
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. Passive acoustical monitoring
can be used in conjunction with visual observations to improve
detection, identification, and localization of cetaceans. The passive
acoustic monitoring would 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 would monitor
the system in real time so that he/she can advise the visual observers
if they acoustic detect cetaceans.
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 would deploy the array from a
winch located on the back deck. A deck cable would connect the tow
cable to the electronics unit in the main computer lab where the
acoustic station, signal conditioning, and processing system would be
located. The acoustic signals received by the hydrophones are
amplified, digitized, and then processed by the Pamguard software. The
system
[[Page 10156]]
can detect marine mammal vocalizations at frequencies up to 250 kHz.
One acoustic observer, an expert bioacoustician with primary
responsibility for the passive acoustic monitoring system would be
aboard the LANGSETH in addition to the four visual observers. The
acoustic observer would 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 would 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 would be on shift for one to six hours at a time. The
other observers would rotate as an acoustic observer, although the
expert acoustician would 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 would
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 would enter the information regarding the call into a
database. Data entry would 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 would 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 would 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 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 would 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 would submit a report to us and to the Foundation
within 90 days after the end of the cruise. The report would describe
the operations that were conducted and sightings of marine mammals and
turtles near the operations. The report would provide full
documentation of methods, results, and interpretation pertaining to all
monitoring. The 90-day report would summarize the dates and locations
of seismic operations, and all marine mammal sightings (dates, times,
locations, activities, associated seismic survey activities). The
report would 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 not permitted by the
authorization (if issued), such as an injury, 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. 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 MMPA 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
[[Page 10157]]
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. 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 would 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 would 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,
within 24 hours of the discovery. The Observatory would 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
MMPA defines ``harassment'' as: Any act of pursuit, torment, or
annoyance which (i) has the potential to injure a marine mammal or
marine mammal stock in the wild [Level A harassment]; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment].
We propose to authorize take by Level B harassment for the proposed
seismic survey. Acoustic stimuli (i.e., increased underwater sound)
generated during the operation of the seismic airgun array may have the
potential to result in the behavioral disturbance of some marine
mammals. There is no evidence that planned activities could result in
serious injury or mortality within the specified geographic area for
the requested authorization. The required mitigation and monitoring
measures would minimize any potential risk for 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 estimates are based on a consideration of
the number of marine mammals that could be harassed by seismic
operations with the 36-airgun array during approximately 5,572 km\2\
(2,151 mi\2\) of transect lines on the Mid-Atlantic Ridge in the north
Atlantic Ocean, as depicted in Figure 1 of the application.
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).
Density Information--The Observatory based the density estimates on
information calculated from sightings, effort, mean group sizes, and
values for f(0) for the southern part of the survey area in Waring et
al. (2008), which extends from the Azores at approximately 38[deg] N to
53[deg] N. The allocated densities calculated for undifferentiated
``common/striped dolphins'' to common and striped dolphins in
proportion to the calculated densities of the two species. The density
calculated for ``unidentified dolphin'' was allocated to bottlenose,
Atlantic spotted, and Risso's dolphins, species that could occur in the
proposed survey area based on their presence in the Azores, in
proportion to the number of sightings in the OBIS database for those
species around the Azores. The density calculated for ``unidentified
small whale'' was allocated to the false killer whale, the one small
whale species that could occur in the proposed survey area based on its
presence in the Azores. The four ``long-finned/short-finned pilot
whales'' sighted in the southern part of the survey area by Waring et
al. (2008) were assumed to be short-finned pilot whales based on OBIS
sightings around the Azores. The density calculated for the one ``sei/
Bryde's whale'' sighting in the southern part of the survey area was
allocated to sei and Bryde's whales in equal proportions. The authors'
calculated value of f(0) for the sei whale was used for calculating
densities of Bryde's, fin, and blue whales, and that for ``small
Delphinidae'' was used for calculating densities of Mesoplodon spp.,
dolphins, the false killer whale, and the short-finned pilot whale.
Because the survey effort in the southern stratum of Waring et al.
(2008) is limited (1,047 km; 650 mi), the survey area is north of the
proposed seismic area (38-52[deg] N versus 36-36.5[deg] N), and the
survey was conducted during a somewhat different season (June versus
April-May), there is some uncertainty about the representativeness of
the data and the assumptions used in the calculations.
Exposure Estimation--The Observatory estimated 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 on one
or more occasions by considering the total marine area that would be
within the 160-dB radius around the operating airgun array on at least
one occasion and the expected density of marine mammals. The number of
possible exposures (including repeat exposures of the same individuals)
can be estimated by considering the total marine area that would be
within the 160-dB radius around the operating airguns, excluding areas
of overlap. Some individuals may be exposed multiple times since the
survey tracklines are spaced close together, however, it is unlikely
that a particular animal would stay in the area during the entire
survey.
The number of different individuals potentially exposed to received
levels greater than or equal to 160 re: 1 [micro]Pa (rms) was
calculated by multiplying:
(1) The expected species density (in number/km\2\), times
(2) The anticipated area to be ensonified to that level during
airgun operations (5,571 km\2\; (2,151 mi\2\).
[[Page 10158]]
The Observatory's estimates of exposures to various sound levels
assume that the proposed surveys would be carried out in full (i.e.,
approximately 20 days of seismic airgun operations), however, the
ensonified areas calculated using the planned number of line-kilometers
have been increased by 25 percent to accommodate lines that may need to
be repeated, equipment testing, account for repeat exposure, etc. As is
typical during offshore ship surveys, inclement weather and equipment
malfunctions are likely to cause delays and may limit the number of
useful line-kilometers of seismic operations that can be undertaken.
Table 3--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 Seismic Survey Over the Mid-Atlantic Ridge in the North Atlantic Ocean,
During April Through June, 2013
----------------------------------------------------------------------------------------------------------------
Estimated number of
individuals exposed Requested or Approx.
Species to sound levels adjusted take Regional percent of
>=160 dB re: 1 authorization population \3\ regional
[micro]Pa\1\ \2\ population \3\
----------------------------------------------------------------------------------------------------------------
Mysticetes:
North Atlantic right whale........... 0 0 0 0
Humpback whale....................... 0 \4\ 2 0 0
Minke whale.......................... 0 \4\ 3 0 0
Bryde's whale........................ 1 1 N/A N/A
Sei whale............................ 1 1 13,000 0.01
Fin whale............................ 25 25 24,887 0.10
Blue whale........................... 8 8 937 0.89
Odontocetes ................... 21 .............. 0.16
Sperm whale.......................... 21 ................ 13,190 ..............
Pygmy sperm whale.................... 0 0 395 0
Dwarf sperm whale.................... 0 0 395 0
Cuvier's beaked whale................ 0 \4\ 7 3,513 0.2
Mesoplodon spp....................... ................... ................ .............. ..............
True's beaked whale.................. ................... ................ .............. ..............
Gervais beaked whale................. 39 39 .............. 1.12
Sowerby's beaked whale............... ................... ................ .............. ..............
Blainville's beaked whale............ ................... ................ 3,502 ..............
Northern bottlenose whale............ 0 \4\ 4 ~40,000 0
Rough-toothed dolphin................ 0 0 N/A 0
Common bottlenose dolphin............ 47 47 81,588 0.06
Pantropical spotted dolphin.......... 0 0 4,439 0
Atlantic spotted dolphin............. 112 112 50,978 0.22
Striped dolphin...................... 1,034 1,034 94,462 1.09
Short-beaked common dolphin.......... 2,115 2,115 120,741 1.75
Risso's dolphin...................... 21 21 20,479 0.10
Pygmy killer whale................... 0 0 N/A 0
False killer whale................... 7 7 N/A N/A
Killer whale......................... 0 \4\ 5 N/A 0
Long-finned pilot whale.............. 0 0 780,000 0
Short-finned pilot whale............. 674 674 780,000 0.09
----------------------------------------------------------------------------------------------------------------
N/A = Not Available.
\1\ Estimates are based on densities in Table 2 and an ensonified area of (5,571 km\2\; (2,151 mi\2\)
\2\ Requested or adjusted take includes a 25 percent contingency for repeated exposures due to the overlap of
parallel survey tracks.
\3\ Regional population size estimates are from Table 2.
\4\ Requested take authorization increased to group size for species for which densities were not calculated but
for which there were OBIS sightings around the Azores.
Encouraging and Coordinating Research
The Observatory would coordinate the planned marine mammal
monitoring program associated with the seismic survey on the Mid-
Atlantic Ridge in the north Atlantic 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 and based on the
following factors, 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. They include:
[[Page 10159]]
(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
(including power-downs and shutdowns); and
(3) 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 behavioral
disturbance to occur during the conduct of the survey activities.
Table 4 in this document outlines 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 survey would last no more than 20 days.
Additionally, the seismic survey would be increasing sound levels in
the marine environment in a relatively small area surrounding the
vessel (compared to the range of the animals), which is constantly
travelling over distances, and some animals may only be exposed to and
harassed by sound for shorter less than day.
Of the 28 marine mammal species under our jurisdiction that are
known to occur or likely to occur in the study area, six of these
species are listed as endangered under the ESA, including: The blue,
fin, humpback, north Atlantic right, sei, and sperm whales. These
species are also categorized as depleted under the MMPA. With the
exception of the north Atlantic right whale, the Observatory has
requested authorized take for these listed species.
As mentioned previously, we estimate that 28 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 take numbers are small (most estimates are less than or
equal to two percent) 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 Table
4 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 a proposed survey on the Mid-Atlantic Ridge in the north
Atlantic Ocean in international waters, from April 2013 through June
2013, may result, at worst, in a modification in behavior and/or low-
level physiological effects (Level B harassment) of certain species of
marine mammals.
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 and sporadic duration of the
research activities, have led us to preliminary determine that this
action would 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 planned research
activities would 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 would 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 (on the Mid-Atlantic Ridge in the
north Atlantic Ocean in international waters) 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 Atlantic right,
sei, and sperm whales. The Observatory did not request take of
endangered north Atlantic 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. Both
agencies would conclude the formal section 7 consultation (with a
single Biological Opinion for the Foundation's Division of Ocean
Sciences and NMFS' Office of Protected Resources, Permits and
Conservation Division federal actions) 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
mandatory Terms and Conditions of the Opinion's Incidental Take
Statement which would incorporate the mitigation and monitoring
requirements included
[[Page 10160]]
in the Incidental Harassment Authorization.
National Environmental Policy Act (NEPA)
To meet our NEPA requirements for the issuance of an IHA to the
Observatory, we intend to prepare an Environmental Assessment (EA)
titled ``Issuance of an Incidental Harassment Authorization to the
Lamont-Doherty Earth Observatory to Take Marine Mammals by Harassment
Incidental to a Marine Geophysical on the Mid-Atlantic Ridge in the
north Atlantic Ocean, from April 2013 through June 2013.'' This EA
would incorporate as appropriate the Foundation's Environmental
Analysis Pursuant To Executive Order 12114 (NSF, 2010) titled, ``Marine
geophysical survey by the R/V MARCUS G. Langseth on the mid-Atlantic
Ridge, April-May 2013,'' by reference pursuant to 40 CFR 1502.21 and
NOAA Administrative Order (NAO) 216-6 Sec. 5.09(d). Prior to making a
final decision on the IHA application, we would decide whether or not
to issue a Finding of No Significant Impact (FONSI).
The Foundation's environmental analysis is available for review at
the addresses set forth earlier in this notice. This notice and the
documents it references provide all relevant environmental information
related to our proposal to issue the IHA. We invite the public's
comment and will consider any comments related to environmental effects
related to the proposed issuance of the IHA submitted in response to
this as we conduct and finalize our NEPA analysis.
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 on the Mid-Atlantic Ridge in the north
Atlantic Ocean from April 2013, through June 2013, 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: February 6, 2013.
Matthew J. Brookhart,
Acting Director, Office of Protected Resources, National Marine
Fisheries Service.
[FR Doc. 2013-03321 Filed 2-12-13; 8:45 am]
BILLING CODE 3510-22-P