Takes of Marine Mammals Incidental to Specified Activities; Low-Energy Marine Geophysical Survey in the Southwest Pacific Ocean, East of New Zealand, May to June 2015, 15059-15097 [2015-06261]
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Vol. 80
Friday,
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March 20, 2015
Part II
Department of Commerce
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National Oceanic and Atmospheric Administration
Takes of Marine Mammals Incidental to Specified Activities; Low-Energy
Marine Geophysical Survey in the Southwest Pacific Ocean, East of New
Zealand, May to June 2015; Notice
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Federal Register / Vol. 80, No. 54 / Friday, March 20, 2015 / Notices
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XD727
Takes of Marine Mammals Incidental to
Specified Activities; Low-Energy
Marine Geophysical Survey in the
Southwest Pacific Ocean, East of New
Zealand, May to June 2015
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; proposed Incidental
Harassment Authorization; request for
comments.
AGENCY:
NMFS has received an
application from the Scripps Institution
of Oceanography (SIO), on behalf of SIO
and the U.S. National Science
Foundation (NSF), for an Incidental
Harassment Authorization (IHA) to take
marine mammals, by harassment,
incidental to conducting a low-energy
marine geophysical (seismic) survey in
the Southwest Pacific Ocean, East of
New Zealand, May to June 2015.
Pursuant to the Marine Mammal
Protection Act (MMPA), NMFS is
requesting comments on its proposal to
issue an IHA to SIO to incidentally
harass, by Level B harassment only, 32
species of marine mammals during the
specified activity.
DATES: Comments and information must
be received no later than April 20, 2015.
ADDRESSES: Comments on the
application should be addressed to Jolie
Harrison, Chief, Permits and
Conservation Division, Office of
Protected Resources, National Marine
Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910. The
mailbox address for providing email
comments is ITP.Goldstein@noaa.gov.
Please include 0648–XD727 in the
subject line. NMFS is not responsible
for email comments sent to addresses
other than the one provided here.
Comments sent via email, including all
attachments, must not exceed a 25megabyte file size.
Instructions: All comments received
are a part of the public record and will
generally be posted to: https://
www.nmfs.noaa.gov/pr/permits/
incidental/ without change. All Personal
Identifying Information (for example,
name, address, etc.) voluntarily
submitted by the commenter may be
publicly accessible. Do not submit
Confidential Business Information or
otherwise sensitive or protected
information.
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SUMMARY:
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A copy of the IHA application may be
obtained by writing to the address
specified above, telephoning the contact
listed here (see FOR FURTHER
INFORMATION CONTACT) or visiting the
Internet at: https://www.nmfs.noaa.gov/
pr/permits/incidental/. Documents cited
in this notice may also be viewed by
appointment, during regular business
hours, at the aforementioned address.
A ‘‘Draft Environmental Analysis of a
Low-Energy Marine Geophysical Survey
by the R/V Roger Revelle in the
Southwest Pacific Ocean, East of New
Zealand, May to June 2015’’ (Draft
Environmental Analysis) in accordance
with the National Environmental Policy
Act (NEPA) and the regulations
published by the Council of
Environmental Quality (CEQ), has been
prepared on behalf of NSF and SIO. It
is posted at the foregoing site. NMFS
has independently evaluated the Draft
Environmental Analysis and has
prepared a separate NEPA analysis
titled ‘‘Draft Environmental Assessment
on the Issuance of an Incidental
Harassment Authorization to the
Scripps Institution of Oceanography to
Take Marine Mammals by Harassment
Incidental to a Low-Energy Marine
Geophysical Survey in the Southwest
Pacific Ocean, East of New Zealand,
May to June 2015.’’ Information in the
SIO’s IHA application, Draft
Environmental Analysis, Draft EA and
this notice of the proposed IHA
collectively provide the environmental
information related to proposed
issuance of the IHA for public review
and comment. NMFS will review all
comments submitted in response to this
notice as we complete the NEPA
process, including a decision of whether
to sign a Finding of No Significant
Impact (FONSI), prior to a final decision
on the IHA request.
FOR FURTHER INFORMATION CONTACT:
Howard Goldstein or Jolie Harrison,
Office of Protected Resources, NMFS,
301–427–8401.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the
MMPA, (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce (Secretary)
to allow, upon request, the incidental,
but not intentional, taking of small
numbers of marine mammals by United
States citizens who engage in a specified
activity (other than commercial fishing)
within a specified geographical region if
certain findings are made and either
regulations are issued or, if the taking is
limited to harassment, a notice of a
proposed authorization is provided to
the public for review.
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An authorization for incidental
takings shall be granted if NMFS finds
that the taking will have a negligible
impact on the species or stock(s), will
not have an unmitigable adverse impact
on the availability of the species or
stock(s) for subsistence uses (where
relevant), and if the permissible
methods of taking and requirements
pertaining to the mitigation, monitoring
and reporting of such takings are set
forth. NMFS has defined ‘‘negligible
impact’’ in 50 CFR 216.103 as ‘‘. . . an
impact resulting from the specified
activity that cannot be reasonably
expected to, and is not reasonably likely
to, adversely affect the species or stock
through effects on annual rates of
recruitment or survival.’’
Section 101(a)(5)(D) of the MMPA
established an expedited process by
which citizens of the United States can
apply for an authorization to
incidentally take small numbers of
marine mammals by harassment.
Section 101(a)(5)(D) of the MMPA
establishes a 45-day time limit for
NMFS’s review of an application,
followed by a 30-day public notice and
comment period on any proposed
authorizations for the incidental
harassment of small numbers of marine
mammals. Within 45 days of the close
of the public comment period, NMFS
must either issue or deny the
authorization.
Except with respect to certain
activities not pertinent here, the MMPA
defines ‘‘harassment’’ as: any act of
pursuit, torment, or annoyance which (i)
has the potential to injure a marine
mammal or marine mammal stock in the
wild [Level A harassment]; or (ii) has
the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment].
Summary of Request
On December 15, 2014, NMFS
received an application from SIO, on
behalf of SIO and NSF, requesting that
NMFS issue an IHA for the take, by
Level B harassment only, of small
numbers of marine mammals incidental
to conducting a low-energy marine
seismic survey as well as heat-flow
measurements in the Southwest Pacific
Ocean, at three sites off the east coast of
New Zealand, during May to June 2015.
The sediment coring component of the
proposed project, which was described
in the IHA application and Draft
Environmental Analysis, was not
funded and no piston or gravity coring
for seafloor samples would be
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conducted during the low-energy
seismic survey. The low-energy seismic
survey would take place within the
Exclusive Economic Zone (EEZ) and
outside the territorial waters of New
Zealand. On behalf of SIO, the U.S.
Department of State is seeking
authorization from New Zealand for
clearance to work within the EEZ.
The research would be conducted by
Oregon State University and funded by
the U.S. National Science Foundation
(NSF). SIO plan to use one source
vessel, the R/V Roger Revelle (Revelle),
and a seismic airgun array and
hydrophone streamer to collect seismic
data in the Southwest Pacific Ocean,
East of New Zealand. SIO plans to use
conventional low-energy, seismic
methodology to perform marine-based
studies in the Southwest Pacific Ocean
(see Figure 1 of the IHA application).
The studies would involve a low-energy
seismic survey and heat-flow
measurements from the seafloor to meet
a number of research goals. In addition
to the proposed operations of the
seismic airgun array and hydrophone
streamer, SIO intends to operate two
additional acoustical data acquisition
systems—a multi-beam echosounder
and sub-bottom profiler continuously
throughout the low-energy seismic
survey.
Acoustic stimuli (i.e., increased
underwater sound) generated during the
operation of the seismic airgun array
have the potential to cause behavioral
disturbance for marine mammals in the
proposed study area. This is the
principal means of marine mammal
taking associated with these activities,
and SIO have requested an
authorization to take 32 species of
marine mammals by Level B
harassment. Take is not expected to
result from the use of the multi-beam
echosounder and sub-bottom profiler, as
the brief exposure of marine mammals
to one pulse, or small numbers of
signals, to be generated by these
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instruments in this particular case is not
likely to result in the harassment of
marine mammals. Also, NMFS does not
expect take to result from collision with
the source vessel because it is a single
vessel moving at a relatively slow,
constant cruise speed of 5 knots ([kts];
9.3 kilometers per hour [km/hr]; 5.8
miles per hour [mph]) during seismic
acquisition within the study area, for a
relatively short period of time
(approximately 27 operational days). It
is likely that any marine mammal would
be able to avoid the vessel.
Description of the Proposed Specified
Activity
Overview
SIO proposes to use one source vessel,
the Revelle, a two GI airgun array and
one hydrophone streamer to conduct the
conventional seismic survey as part of
the NSF-funded research project
‘‘Collaborative Research: The Thermal
Regime of the Hikurangi Subduction
Zone and Shallow Slow Slip Events,
New Zealand.’’ In addition to the
airguns, SIO intends to conduct a
bathymetric survey and heat-flow
measurements at three sites off the
southwest coast of North Island and
northeast coast of South Island, New
Zealand from the Revelle during the
proposed low-energy seismic survey.
Proposed Dates and Duration
The Revelle is expected to depart from
Auckland, New Zealand on
approximately May 18, 2015 and arrive
at Napier, New Zealand on
approximately June 18, 2015. Airgun
operations would take approximately
135 hours in total, and the remainder of
the time would be spent in transit and
collecting heat-flow measurements and
cores. The total distance the Revelle
would travel in the region to conduct
the proposed research activities (i.e.,
seismic survey, bathymetric survey, and
transit to heat-flow measurement
locations) represents approximately
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2,000 km (1,079.9 nmi). Some minor
deviation from this schedule is possible,
depending on logistics and weather
(e.g., the cruise may depart earlier or be
extended due to poor weather; or there
could be additional days of airgun
operations if collected data are deemed
to be of substandard quality).
Proposed Specified Geographic Region
The proposed project and survey sites
are located off the southeast coast of
North Island and northeast coast of the
South Island, New Zealand in selected
regions of the Southwest Pacific Ocean.
The proposed survey sites are located
between approximately 38.5 to 42.5°
South and approximately 174 to 180°
East off the east coast of New Zealand,
in the EEZ of New Zealand and outside
of territorial waters (see Figure 1 of the
IHA Application). Water depths in the
study area are between approximately
200 to 3,000 m (656.2 to 9,842.5 ft). The
proposed low-energy seismic survey
would be collected in a total of nine
grids of intersecting lines of two sizes
(see Figure 1 of the IHA application) at
exact locations to be determined in the
field during May to June 2015. Figure 1
also illustrates the general bathymetry of
the proposed study area. The proposed
low-energy seismic survey would be
within an area of approximately 1,154
km2 (336.5 nmi2). This estimate is based
on the maximum number of kilometers
for the low-energy seismic survey (1,250
km) multiplied by the area ensonified
around the planned tracklines (2 x 0.6
km in intermediate water depths and
2 x 0.4 km in deep water depths). The
ensonified area is based on the
predicted rms radii (m) based on
modeling and empirical measurements
(assuming 100% use of the two 45 in3
GI airguns in 100 to 1,000 m or greater
than 1,000 m water depths), which was
calculated to be 600 m (1,968.5 ft) or
400 m (1,312.3 ft).
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Detailed Description of the Proposed
Specified Activity
In support of a research project put
forward by Oregon State University
(OSU) and to be funded by NSF, SIO
proposes to conduct a low-energy
seismic survey in the Southwest Pacific
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Ocean, East of New Zealand, from May
to June 2015. In addition to the lowenergy seismic survey, scientific
research activities would include
conducting a bathymetric profile survey
of the seafloor using transducer-based
instruments such as a multi-beam
echosounder and sub-bottom profiler;
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and heat-flow measurements from the
seafloor using various methods and
equipment at three sites off the
southeast coast of North Island and
northeast coast of South Island, New
Zealand. Water depths in the survey
area are approximately 200 to 3,000
meters (m) (656.2 to 9,842.5 feet [ft]).
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Figure 1. Locations of the proposed low-energy seismic survey and heat-flow probe
measurement sites east ofNew Zealand, May to June 2015.
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The proposed low-energy seismic
survey is scheduled to occur for a total
of approximately 135 hours over the
course of the entire cruise, which would
be for approximately 27 operational
days in May to June 2015. The proposed
low-energy seismic survey would be
conducted during the day (from nautical
twilight-dawn to nautical twilight-dusk)
and night, and for up to approximately
72 hours of continuous operations at a
time. The operation hours and survey
length would include equipment
testing, ramp-up, line changes, and
repeat coverage. Some minor deviation
from these dates would be possible,
depending on logistics and weather. The
Principal Investigators are Dr. R. N.
Harris and Dr. A. Trehu of the OSU.
The proposed surveys would allow
the development of a process-based
understanding of the thermal structure
of the Hikurangi subduction zone, and
the expansion of this understanding by
using regional observations of gas
hydrate-related bottom simulating
reflections. To achieve the proposed
project’s goals, the Principal
Investigators propose to collect lowenergy, high-resolution multi-channel
system profiles, heat-flow
measurements, and sediment cores
along transects seaward and landward
of the Hikurangi deformation front.
Heat-flow measurements would be
made in well-characterized sites,
increasing the number of publicly
available heat-flow and thermal
conductivity measurements from this
continental margin by two orders of
magnitude. Seismic survey data would
be used to produce sediment structural
maps and seismic velocities to achieve
the project objectives. Data from
sediment cores would detect and
estimate the nature and sources of fluid
flow through high permeability
pathways in the overriding plate and
along the subduction thrust;
characterize the hydrocarbon and gas
hydrate system to assist with estimates
of heat flow from Bottom Simulating
Reflectors (BSR)s, their role in slope
stability, and fluid source; and elucidate
the response of microbes involved in
carbon cycling to changes in methane
flux.
The low-energy seismic survey would
be collected in a total of 9 grids of
intersecting lines of two sizes (see
Figure 1 of the IHA application) at exact
locations to be determined in the field.
The water depths would be very similar
to those at the nominal survey locations
shown in Figure 1 of the IHA
application. The northern and middle
sites off the North Island would be the
primary study areas, and the southern
site off the South Island would be a
contingency area that would only be
surveyed if time permits. SIO’s
calculations assume that 7 grids at the
primary areas and two grids at the
southern site would be surveyed. The
total trackline distance of the lowenergy seismic survey would be
approximately 1,250 km (including the
two South Island contingency sites),
almost all in water depths greater than
1,000 m.
The procedures to be used for the
survey would be similar to those used
during previous low-energy seismic
surveys by SIO and NSF and would use
conventional seismic methodology. The
proposed survey would involve one
source vessel, the Revelle. SIO would
deploy a two Sercel Generator Injector
(GI) airgun array (each with a discharge
volume of 45 in3 [290.3 cm3], in one
string, with a total volume of 90 in3
[580.6 cm3]) as an energy source, at a
tow depth of up to 2 m (6.6 ft) below
the surface (more information on the
airguns can be found in SIO’s IHA
application). The airguns in the array
would be spaced approximately 8 m
(26.2 ft) apart and 21 m (68.9 ft) astern
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of the vessel. The receiving system
would consist of one 600 m (1,968.5 ft)
long, 48-channel hydrophone
streamer(s) towed behind the vessel.
Data acquisition is planned along a
series of predetermined lines, almost all
(approximately 95%) of which would be
in water depths greater than 1,000 m. As
the GI airguns are towed along the
survey lines, the hydrophone streamer
would receive the returning acoustic
signals and transfer the data to the
onboard processing system. The seismic
surveys would be conducted while the
heat-flow probe is being recharged. All
planned seismic data acquisition
activities would be conducted by
technicians provided by SIO, with
onboard assistance by the scientists who
have proposed the study. The vessel
would be self-contained, and the crew
would live aboard the vessel for the
entire cruise.
The planned seismic survey
(including equipment testing, start-up,
line changes, repeat coverage of any
areas, and equipment recovery) would
consist of approximately 1,250
kilometers (km) (674.9 nautical miles
[nmi]) of transect lines (including turns)
in the study area in the Southwest
Pacific Ocean (see Figures 1 of the IHA
application). Approximately 95% of the
low-energy seismic survey would occur
in water depths greater than 1,000 m. In
addition to the operation of the airgun
array and heat-flow measurements, a
multi-beam echosounder and a subbottom profiler would also likely be
operated from the Revelle continuously
throughout the cruise. There would be
additional airgun operations associated
with equipment testing, ramp-up, and
possible line changes or repeat coverage
of any areas where initial data quality is
sub-standard. In SIO’s estimated take
calculations, 25% has been added for
those additional operations.
TABLE 1—PROPOSED LOW-ENERGY SEISMIC SURVEY ACTIVITIES IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW
ZEALAND
Survey length
(km)
Total duration
(hr) 1
1,250 (674.9 nmi) ......
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1 Airgun
∼135
Airgun array total volume
Time between airgun shots
(distance)
2 × 45 = 90 in3 (2 × 1474.8 cm3) .......
6 to 10 seconds (18.5 to 31 m or
60.7 to 101.7 ft).
Streamer length
(m)
600 (1,968.5 ft)
operations are planned for no more than approximately 72 continuous hours at a time.
Vessel Specifications
The Revelle, a research vessel owned
by the U.S. Navy and operated by SIO
of the University of California San
Diego, would tow the two GI airgun
array, as well as the hydrophone
streamer. When the Revelle is towing
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the airgun array and the relatively short
hydrophone streamer, the turning rate of
the vessel while the gear is deployed is
approximately 20 degrees per minute,
which is much higher than the limit of
5 degrees per minute for a seismic
vessel towing a streamer of more typical
length (much greater than 1 km [0.5
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nmi]). Thus, the maneuverability of the
vessel would not be limited much
during operations with the streamer.
The U.S.-flagged vessel, built in 1996,
has a length of 83 m (272.3 ft); a beam
of 16.0 m (52.5 ft); a maximum draft of
5.2 m (19.5 ft); and a gross tonnage of
3,180. The ship is powered by two 3,000
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horsepower (hp) Propulsion General
Electric motors) and a 1,180 hp
azimuthing jet bowthruster. The GI
airgun compressor onboard the vessel is
manufactured by Price Air Compressors.
The Revelle’s operation speed during
seismic acquisition is typically
approximately 9.3 km/hr (5 kts) (varying
between 7.4 to 11.1 km/hr [4 to 6 kts]).
When not towing seismic survey gear,
the Revelle typically cruises at 22.2 to
23.1 km/hr (12 to 12.5 kts) and has a
maximum speed of 27.8 km/hr (15 kts).
The Revelle has an operating range of
approximately 27,780 km (15,000 nmi)
(the distance the vessel can travel
without refueling), which is
approximately 70 to 75 days. The vessel
can accommodate 37 scientists and 22
crew members.
The vessel also has two observation
station locations from which Protected
Species Observers (PSO) would watch
for marine mammals before and during
the proposed airgun operations on the
Revelle. Observing stations would be at
the 02 level, with a PSO’s eye level
approximately 10.4 m (34 ft) above sea
level—one forward on the 02 deck
commanding a forward-centered,
approximately 240° view around the
vessel, and one atop the aft hangar, with
an aft-centered view that includes the
radii around the airguns. The eyes on
the bridge watch would be at a height
of approximately 15 m (49 ft); PSOs
would work on the enclosed bridge and
adjoining aft steering station during any
inclement weather. More details of the
Revelle can be found in the IHA
application and online at: https://
scripps.ucsd.edu/ships/revelle.
Acoustic Source Specifications—
Seismic Airguns
The Revelle would deploy an airgun
array, consisting of two 45 in3 Sercel GI
airguns as the primary energy source
and a 600 m streamer(s) containing
hydrophones. The airgun array would
have a supply firing pressure of 1,750
pounds per square inch (psi). Seismic
pulses for the GI airguns would be
emitted at intervals of approximately 6
to 10 seconds. There would be a
maximum of approximately 360 shots
per hour. The number of shots per hour
would vary based upon the vessel speed
over ground during the low-energy
seismic survey. During firing, a brief
(approximately 20 millisecond) pulse
sound would be emitted; the airguns
would be silent during the intervening
periods. The dominant frequency
components would range from 0 to 188
Hertz (Hz).
The GI airguns would fire the
compressed air volume in unison in
‘‘true GI’’ mode. The GI airguns would
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be used in ‘‘true GI’’ mode, that is, the
volume of the injector chamber (I) (105
in3 [1721 cm3]) of each GI airgun is
greater to that of its generator chamber
(G) (45 in3 [737 cm3]) for each airgun.
The generator chamber of each GI airgun
(45 in3) would be the primary source
and the one responsible for introducing
the sound pulse into the ocean. The
larger (105 in3) injector chamber injects
air into the previously-generated bubble
to maintain its shape, and would not
introduce more sound into the water.
The two GI airguns would be spaced
approximately 8 m (26.2 ft) apart, sideby-side, 21 m (68.9 ft) behind the
Revelle, at a depth of up to 2 m during
the low-energy seismic survey.
The Nucleus modeling software used
at Lamont-Doherty Earth Observatory of
Columbia University (L–DEO) does not
include GI airguns as part of its airgun
library, however signatures and
mitigation models have been obtained
for two 45 in3 G airguns that are close
approximations. For the two 45 in3
airgun array, the source output
(downward) is 230.6 dB re 1 mPam 0-topeak and 235.8 dB re 1 mPam for peakto-peak. The dominant frequency range
would be 0 to 188 Hz for a pair of GI
airguns towed at 2 m depth.
During the low-energy seismic survey,
the vessel would attempt to maintain a
constant cruise speed of approximately
5 knots. The airguns would operate
continuously for no more than
approximately 72 hours at a time based
on operational constraints. The total
duration of the airgun operations would
not exceed 135 hours. The relatively
short, 48-channel hydrophone streamer
would provide operational flexibility to
allow the low-energy seismic survey to
proceed along the designated cruise
tracklines. The design of the seismic
equipment is to achieve high-resolution
images with the ability to correlate to
the ultra-high frequency sub-bottom
profiling data and provide crosssectional views to pair with the seafloor
bathymetry.
Metrics Used in This Document
This section includes a brief
explanation of the sound measurements
frequently used in the discussions of
acoustic effects in this document. Sound
pressure is the sound force per unit
area, and is usually measured in
micropascals (mPa), where 1 pascal (Pa)
is the pressure resulting from a force of
one newton exerted over an area of one
square meter. Sound pressure level
(SPL) is expressed as the ratio of a
measured sound pressure and a
reference level. The commonly used
reference pressure level in underwater
acoustics is 1 mPa, and the units for
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SPLs are dB re 1 mPa. SPL (in decibels
[dB]) = 20 log (pressure/reference
pressure).
SPL is an instantaneous measurement
and can be expressed as the peak, the
peak-to-peak (p-p), or the root mean
square (rms). Root mean square, which
is the square root of the arithmetic
average of the squared instantaneous
pressure values, is typically used in
discussions of the effects of sounds on
vertebrates and all references to SPL in
this document refer to the root mean
square unless otherwise noted. SPL does
not take the duration of a sound into
account.
Characteristics of the Airgun Pulses
Airguns function by venting highpressure air into the water, which
creates an air bubble. The pressure
signature of an individual airgun
consists of a sharp rise and then fall in
pressure, followed 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 downward-directed
source levels of the airgun arrays used
by SIO on the Revelle do not represent
actual sound levels that can be
measured at any location in the water.
Rather, they represent the level that
would be found 1 m (3.3 ft) from a
hypothetical point source emitting the
same total amount of sound as is
emitted by the combined GI airguns.
The actual received level at any location
in the water near the GI airguns would
not exceed the source level of the
strongest individual source. In this case,
that would be about 224.6 dB re 1 mPam
peak or 229.8 dB re 1 mPam peak-topeak for the two 45 in3 airgun array.
However, the difference between rms
and peak or peak-to-peak values for a
given pulse depends on the frequency
content and duration of the pulse,
among other factors. Actual levels
experienced by any organism more than
1 m from either GI airgun would be
significantly lower.
Accordingly, L–DEO has predicted
and modeled the received sound levels
in relation to distance and direction
from the two GI airgun array. These are
the nominal source levels applicable to
downward propagation. A detailed
description of L–DEO’s modeling for
this survey’s marine seismic source
arrays for protected species mitigation is
provided in the ‘‘Programmatic
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Environmental Impact Statement/
Overseas Environmental Impact
Statement prepared for Marine Seismic
Research that is funded by the National
Science Foundation and conducted by
the U.S. Geological Survey’’ (NSF/USGS
PEIS, 2011). The NSF/USGS PEIS
discusses the characteristics of the
airgun pulses. NMFS refers the
reviewers to that document for
additional information.
Predicted Sound Levels for the Airguns
To estimate takes and determine
mitigation (i.e., buffer and exclusion)
zones for the airgun array to be used,
received sound levels have been
modeled by L–DEO for a number of
airgun configurations, including two 45
in3 G airguns, in relation to distance and
direction from the airguns (see Figure 2
of the IHA application). The model does
not allow for bottom interactions, and is
most directly applicable to deep water.
Because the model results are for G
airguns, which have more energy than
GI airguns of the same size, those
distances overestimate (by
approximately 10%) the distances for
the two 45 in3 GI airguns. Although the
distances are overestimated, no
adjustments for this have been made to
the radii distances in Table 2 (below).
Based on the modeling, estimates of the
maximum distances from the GI airguns
where sound levels of 190, 180, and 160
dB re 1 mPa (rms) are predicted to be
received in intermediate and deep water
are shown in Table 2 (see Table 1 of the
IHA application).
Empirical data concerning the 190,
180, and 160 dB (rms) distances were
acquired for various airgun arrays based
on measurements during the acoustic
verification studies conducted by L–
DEO in the northern Gulf of Mexico
(GOM) in 2003 (Tolstoy et al., 2004) and
2007 to 2008 (Tolstoy et al., 2009;
Diebold et al., 2010). Results of the 18
and 36 airgun array are not relevant for
the two GI airguns to be used in the
proposed low-energy seismic survey
because the airgun arrays are not the
same size or volume. The empirical data
for the 6, 10, 12, and 20 airgun arrays
indicate that, for deep water, the L–DEO
model tends to overestimate the
received sound levels at a given
distance (Tolstoy et al., 2004). For the
two G airgun array, measurements were
obtained only in shallow water. When
compared to measurements in acquired
in deep water, mitigation radii provided
by the L–DEO model for the proposed
airgun operations were found to be
conservative. The acoustic verification
surveys also showed that distances to
given received levels vary with water
depth; these are larger in shallow water,
while intermediate/slope environments
show characteristics intermediate
between those of shallow water and
those of deep water environments, and
documented the influence of a sloping
seafloor. The only measurements
obtained for intermediate depths during
either survey were for the 36-airgun
array in 2007 to 2008 (Diebold et al.,
2010). Following results obtained at this
site and earlier practice, a correction
factor of 1.5, irrespective of distance to
the airgun array, is used to derive
intermediate-water radii from modeled
deep-water radii.
Measurements were not made for a
two GI airgun array in intermediate and
deep water; however, SIO proposes to
use the buffer and exclusion zones
predicted by L–DEO’s model for the
proposed GI airgun operations in
intermediate and deep water, although
they are likely conservative given the
empirical results for the other arrays.
Using the L–DEO model, Table 2
(below) shows the distances at which
three rms sound levels are expected to
be received from the two GI airguns.
The 160 dB re 1 mPam (rms) isopleth is
the threshold specified by NMFS for
potential Level B (behavioral)
harassment from impulsive noise for
both cetaceans and pinnipeds. The 180
and 190 dB re 1 mPam (rms) isopleths
are the thresholds currently used to
estimate potential Level A harassment
as specified by NMFS (2000) and are
applicable to cetaceans and pinnipeds,
respectively. Table 2 summarizes the
predicted distances at which sound
levels (160, 180, and 190 dB [rms]) are
expected to be received from the two
airgun array (each 45 in3) operating in
intermediate water (100 to 1,000 m
[328.1 to 3,280 ft]) and deep water
(>1,000 m) depths.
TABLE 2—PREDICTED AND MODELED (TWO 45 IN3 GI AIRGUN ARRAY) DISTANCES TO WHICH SOUND LEVELS ≥160, 180,
AND 190 dB RE 1 μPA (rms) COULD BE RECEIVED IN INTERMEDIATE AND DEEP WATER DURING THE PROPOSED
LOW-ENERGY SEISMIC SURVEY IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND, MAY TO JUNE 2015
Source and total volume
Two 45 in3 GI Airguns
(90 in3).
Two 45 in3 GI Airguns
(90 in3).
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Predicted RMS radii distances (m) for 2 GI airgun array
Tow depth
(m)
2
2
Water depth (m)
160 dB
Intermediate (100 to
1,000).
Deep (>1,000) .............
Based on the NSF/USGS PEIS and
Record of Decision, for situations which
incidental take of marine mammals is
anticipated, proposed exclusion zones
of 100 m for cetaceans and pinnipeds
for all low-energy acoustic sources in
water depths greater than 100 m would
be implemented.
NMFS expects that acoustic stimuli
resulting from the proposed operation of
the two GI airgun array has the potential
to harass marine mammals. NMFS does
not expect that the movement of the
Revelle, during the conduct of the lowenergy seismic survey, has the potential
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180 dB
190 dB
600 (1,968.5
ft)
400 (1,312.3
ft)
100 (328.1 ft)
15 (49.2 ft) *100 would be used for pinnipeds
as described in NSF/USGS PEIS*
10 (32.8 ft) *100 would be used for pinnipeds
as described in NSF/USGS PEIS*
100 (328.1
m)
to harass marine mammals because the
relatively slow operation speed of the
vessel (approximately 5 kts; 9.3 km/hr;
5.8 mph) during seismic data
acquisition should allow marine
mammals to avoid the vessel.
Bathymetric Survey
Along with the low-energy airgun
operations, two additional geophysical
(detailed swath bathymetry)
measurements focused on a specific
study area within the Southwest Pacific
Ocean would be made using hullmounted sonar system instruments from
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the Revelle for operational and
navigational purposes. The ocean floor
would be mapped with the Kongsberg
EM 122 multi-beam echosounder and a
Knudsen Chirp 3260 sub-bottom
profiler. During bathymetric survey
operations, when the vessel is not
towing seismic equipment, its average
speed would be approximately 10.1 kts
(18.8 km/hr). In cases where higher
resolution bathymetric data is sought,
the average speed may be as low as 5 kts
(9.3 km/hr). These sound sources would
be operated continuously from the
Revelle throughout the cruise. Operating
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characteristics for the instruments to be
used are described below.
Multi-Beam Echosounder (Kongsberg
EM 122)—The hull-mounted multibeam sonar would be operated
continuously during the cruise to map
the ocean floor. This instrument would
operate at a frequency of 10.5 to 13
(usually 12) kilohertz (kHz) and would
be hull-mounted. The transmitting
beamwidth would be 1 or 2° fore to aft
and 150° athwartship (cross-track). The
estimated maximum source energy level
would be 242 dB re 1mPa (rms). Each
‘ping’ of eight (in water greater than
1,000 m or four (in water less than 1,000
m) successive fan-shaped transmissions,
each ensonifying a sector that extends 1°
fore to aft. Continuous-wave signals
increase from 2 to 15 milliseconds (ms)
in water depths up to 2,600 m (8,530 ft),
and FM chirp signals up to 100 ms long
would be used in water greater than
2,600 m. The successive transmission
span an overall cross-track angular
extent of about 150°, with 2 ms gaps
between the pings for successive
sectors.
Sub-Bottom Profiler—The Revelle
would operate a Knudsen 3260 subbottom profiler continuously throughout
the cruise simultaneously to map and
provide information about the seafloor
sedimentary features and bottom
topography that is mapped
simultaneously with the multi-beam
echosounder. The beam of the subbottom profiler would be transmitted as
a 27° cone, directed downward by a 3.5
kHz transducer in the hull of the
Revelle. The nominal power output
would be 10 kilowatt (kW), but the
actual maximum radiated power would
be 3 kW or 222 dB (rms). The ping
duration would be up to 64 ms, and the
ping interval would be 1 second. A
common mode of operation is a
broadcast five pulses at 1 second
intervals followed by a 5 second pause.
The sub-bottom profiler would be
capable of reaching depths of 10,000 m
(32,808.4 ft).
Acoustic Locator (Pinger)—A pinger
would be deployed with certain
instruments and equipment (e.g., heatflow probe) so these devices can be
located in the event they become
detached from their lines. The pinger
used in the heat-flow measurement
activities would be the Datasonics
model BFP–312HP. A pinger typically
operates at a frequency of 32.8 kHz,
generates a 5 ms pulse per second (10
pulses over a 10 second period), and has
an acoustical output of 210 dB re 1 mPa
(rms). The pinger would be used during
heat-flow measurement operations only.
It would operate continuously during
each heat-flow probe deployment. Each
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heat-flow probe measurement would
last approximately 24 hours.
Heat-Flow Probe Deployment
Heat-flow measurements would be
made using a ‘‘violin-bow’’ probe with
11 thermistors that provides real time
(analog) telemetry of the thermal
gradient and in-situ thermal
conductivity. The heat-flow probe that
would be used on the Revelle consists
of a lance 6 centimeter (cm) (2.4 in) in
diameter and 3.5 m (11.5 ft) long, a
sensor tube housing thermistors and
heater wires, and a 560 kg (1,234.6 lb)
weight stand. The probe would be
lowered to the bottom, and a 12 kHz
pinger attached to the wire
approximately 50 m (164 ft) above the
instrument would monitor the distance
between the probe and bottom. The
probe would be driven into the
sediment by gravity, and temperatures
within the sediment would be measured
with equally spaced thermistors. On
completion of a measurement, the
instrument would be hoisted 100 to 500
m (328.1 to 1,640.4 ft) above the
sediment, the ship is maneuvered to a
new position, and the process is
repeated. Heat-flow measurements can
generally be made at a rate of 1 to 2
hours per measurement, approximately
15 minutes for the actual measurement
and 45 to 90 minutes to reposition the
ship and probe. Internal power allows
20 to 24 measurements during a single
lowering of the tool, with profiles
lasting as long as 48 hours. Proposed
heat-flow measurements would have a
nominal spacing of 0.5 to 1 km (0.3 to
0.5 nmi), which would be decreased in
areas of significant basement relief or of
large changes in gradient. Heat flow
transect locations are shown in Figure 1
of the IHA application, and details of
the probe and its deployment are given
in Section (f) of the IHA application. In
total, approximately 200 heat-flow
measurements would be made.
Description of the Marine Mammals in
the Specified Geographic Area of the
Proposed Specified Activity
Few scientific systematic surveys for
marine mammals have been conducted
in the waters of New Zealand, and these
mainly consist of single-species surveys
in shallow coastal waters (e.g., Dawson
et al., 2004; Slooten et al., 2004, 2006).
Large-scale, multi-species marine
mammal surveys are lacking. Various
sources for data on sightings in the
proposed study area were used to
describe the occurrence of marine
mammals in the waters of New Zealand,
such as opportunistic sighting records
presented in previous reports (including
the New Zealand Department of
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Conservation marine mammals sighting
database) considered in evaluating
potential marine mammals in the
proposed action area.
New Zealand is considered a
‘‘hotspot’’ for marine mammal species
richness (Kaschner et al., 2011). The
marine mammals that generally occur in
the proposed action area belong to three
taxonomic groups: Mysticetes (baleen
whales), odontocetes (toothed whales),
and pinnipeds (seals and sea lions). The
marine mammal species that could
potentially occur within the Southwest
Pacific Ocean in proximity to the
proposed action area East of New
Zealand include 30 species of cetaceans
(21 odontocetes and 9 mysticetes) and 2
species of pinnipeds (32 total species of
marine mammals).
Marine mammal species likely to be
encountered in the proposed study area
that are listed as endangered under the
U.S. Endangered Species Act of 1973
(ESA; 16 U.S.C. 1531 et seq.), includes
the southern right (Eubalaena australis),
humpback (Megaptera novaeangliae),
sei (Balaenoptera borealis), fin
(Balaenoptera physalus), blue
(Balaenoptera musculus), and sperm
(Physeter macrocephalus) whale. The
Maui’s dolphin (Cephalorhynchus
hectori maui) and New Zealand sea lion
(Phocartos hookeri) are two other
species are ranked as ‘‘nationally
critical’’ in New Zealand (Baker et al.,
2010). Maui’s dolphin is only found
along the west coast of the North Island.
The northern range of the New Zealand
sea lion is not expected to extend to the
proposed study area based on New
Zealand’s National Aquatic Biodiversity
Information System (NABIS, 2014) and
is not considered further.
In addition to the marine mammal
species known to occur in the
Southwest Pacific Ocean off the east
coast of New Zealand, there are 18
species of marine mammals (12 cetacean
and 6 pinniped species) with ranges that
are known to potentially occur in the
waters of the proposed study area, but
they are categorized as ‘‘vagrant’’ under
the New Zealand Threat Classification
System (Baker et al., 2010). These
include: Dwarf sperm whale (Kogia
sima), Arnoux’s beaked whale
(Berardius arnouxi), ginkgo-toothed
beaked whale (Mesoplodon ginkgodens),
pygmy beaked whale (Mesoplodon
peruvianis), Type B, C, and D killer
whale (Orcinus orca), melon-headed
whale (Peponocephala electra), Risso’s
dolphin (Grampus griseus), Fraser’s
dolphin (Lagenodelphis hosei),
pantropical spotted dolphin (Stenella
attenuata), striped dolphin (Stenella
coeruleoalba), rough-toothed dolphin
(Steno bredanensis), spectacled
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porpoise (Phocoena dioptrica),
Antarctic fur seal (Arctocephalus
gazelle), Subantarctic fur seal
(Arctocephalus tropicalis), crabeater
seal (Lobodon carcinophagus), leopard
seal (Hydrurga leptonyx), Ross seal
(Ommatophoca rossi), and Weddell seal
(Leptonychotes weddellii). According to
Jefferson et al. (2008), the distributional
range of Hubb’s beaked whale
(Mesoplodon carlhubbsi) and True’s
beaked whale (Mesoplodon mirus) may
also include New Zealand waters. There
are no records of Hubb’s beaked whale
in New Zealand, and only a single
record of True’s beaked whale, which
stranded on the west coast of South
Island in November 2011 (Constantine
et al., 2014). The spinner dolphin’s
(Stenella longirostris) range includes
tropical and subtropical zones 40° North
to 40° South, but would be considered
vagrant as well. However, these species
are not expected to occur where the
proposed activities would take place.
These species are not considered further
in this document. Table 3 (below)
presents information on the habitat,
occurrence, distribution, abundance,
population, and conservation status of
the species of marine mammals that
may occur in the proposed study area
during May to June 2015.
TABLE 3—THE HABITAT, OCCURRENCE, RANGE, REGIONAL ABUNDANCE, AND CONSERVATION STATUS OF MARINE MAMMALS THAT MAY OCCUR IN OR NEAR THE PROPOSED LOW-ENERGY SEISMIC SURVEY AREA IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND
[See text and tables 2 in SIO’s IHA application for further details]
Species
Habitat
Occurrence
Range
Population estimate
ESA 1
MMPA 2
Mysticetes
Southern right whale
(Eubalaena australis).
Coastal, shelf, pelagic.
Common ......
Circumpolar 20 to 55°
South.
Pygmy right whale
(Caperea marginata).
Humpback whale
(Megaptera
novaeangliae).
Minke whale (Balaenoptera
acutorostrata including
dwarf sub-species).
Antarctic minke whale
(Balaenoptera
bonaerensis).
Bryde’s whale
(Balaenoptera edeni).
Pelagic and coastal.
Pelagic, nearshore
waters, and
banks.
Pelagic and coastal.
Rare ............
Circumpolar 30 to 55°
South.
Cosmopolitan Migratory ....
Pelagic, ice floes,
coastal.
Uncommon ..
Pelagic and coastal.
Rare ............
Circumglobal—Tropical
and Subtropical Zones.
Sei whale (Balaenoptera
borealis).
Primarily offshore,
pelagic.
Uncommon ..
Fin whale (Balaenoptera
physalus).
Continental slope,
pelagic.
Uncommon ..
Migratory, Feeding Concentration 40 to 50°
South.
Cosmopolitan, Migratory ..
Blue whale (Balaenoptera
musculus; including
pygmy blue whale
[Balaenoptera musculus
brevicauda]).
Pelagic, shelf,
coastal.
Uncommon ..
Common ......
Uncommon ..
Circumpolar—Southern
Hemisphere to 65°
South.
7° South to ice edge (usually 20 to 65° South).
Migratory Pygmy blue
whale—North of Antarctic Convergence 55°
South.
8,000 3 to 15,000 4—
Worldwide 12,000 12—
Southern Hemisphere
2,700 12—Sub-Antarctic
New Zealand.
NA .....................................
EN
D
NL
NC
35,000 to 42,000 3 12—
Southern Hemisphere.
EN
D
720,0000 to
750,000 12 14 15—Southern Hemisphere.
720,000 to
750,000 12 14 15—Southern Hemisphere.
At least 30,000 to
40,000 3—Worldwide
21,000 12—Northwestern
Pacific Ocean 48,109 13.
80,000 3—Worldwide
10,000 14—South of Antarctic Convergence.
140,000 3—Worldwide
15,000 14—South of Antarctic Convergence.
8,000 to 9,000 3—Worldwide 2,300 12—True
Southern Hemisphere
1,500 14—Pygmy.
NL
NC
NL
NC
NL
NC
EN
D
EN
D
EN
D
360,000 3—Worldwide
30,000 13—South of Antarctic Convergence.
NA .....................................
EN
D
NL
NC
NA .....................................
NL
NC
NA .....................................
NL
NC
600,000 14 16 ......................
NL
NC
500,000 3—South of Antarctic Convergence
600,000 14 16.
600,000 14 16 ......................
NL
NC
NL
NC
Odontocetes
Pelagic, deep sea
Common ......
Cosmopolitan, Migratory ...
Dwarf sperm whale (Kogia
sima).
Pygmy sperm whale (Kogia
breviceps).
Arnoux’s beaked whale
(Berardius arnuxii).
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Sperm whale (Physeter
macrocephalus).
Shelf, Pelagic .......
Vagrant .......
Shelf, Pelagic .......
Uncommon ..
Pelagic .................
Vagrant ........
Cuvier’s beaked whale
(Ziphius cavirostris).
Southern bottlenose whale
(Hyperoodon planifrons).
Pelagic .................
Uncommon ..
Circumglobal—Tropical
and Temperate Zones.
Circumglobal—Temperate
Zones.
Circumpolar in Southern
Hemisphere, 24 to 78°
South.
Cosmopolitan ....................
Pelagic .................
Rare ............
Circumpolar—30° South to
ice edge.
Shepherd’s beaked whale
(Tasmacetus shepherdi).
Pelagic .................
Rare ............
Circumpolar—Cold temperate waters Southern
Hemisphere.
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TABLE 3—THE HABITAT, OCCURRENCE, RANGE, REGIONAL ABUNDANCE, AND CONSERVATION STATUS OF MARINE MAMMALS THAT MAY OCCUR IN OR NEAR THE PROPOSED LOW-ENERGY SEISMIC SURVEY AREA IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND—Continued
[See text and tables 2 in SIO’s IHA application for further details]
Habitat
Occurrence
Range
Population estimate
Andrew’s beaked whale
(Mesoplodon bowdoini).
Pelagic .................
Rare ............
600,000 14 16 ......................
NL
NC
Blainville’s beaked whale
(Mesoplodon
densirostris).
Ginkgo-toothed beaked
whale (Mesoplodon
ginkgodens).
Gray’s beaked whale
(Mesoplodon grayi).
Hector’s beaked whale
(Mesoplodon hectori).
Pelagic .................
Rare ............
Circumpolar—temperate
waters of Southern
Hemisphere, 32 to 55°
South.
Circumglobal—tropical and
temperate waters.
600,000 14 16 ......................
NL
NC
Pelagic .................
Vagrant .......
NA .....................................
NL
NC
Pelagic .................
Common ......
600,000 14 16 ......................
NL
NC
Pelagic .................
Rare ............
600,000 14 16 ......................
NL
NC
Hubb’s beaked whale
(Mesoplodon carlhubbsi).
Pygmy beaked whale
(Mesoplodon peruvianis).
Spade-toothed beaked
whale (Mesoplodon
traversii).
Strap-toothed beaked
whale (Mesoplodon
layardii).
True’s beaked whale
(Mesoplodon mirus).
Pelagic .................
Vagrant .......
Tropical and Temperate
waters—Indo-Pacific
Ocean.
30° South to Antarctic
waters.
Circumpolar—cool temperate waters of Southern Hemisphere.
North Pacific Ocean .........
NA .....................................
NL
NC
Pelagic .................
Vagrant .......
NA .....................................
NL
NC
Pelagic .................
Rare ............
600,000 14 16 ......................
NL
NC
Pelagic .................
Uncommon ..
30° South to Antarctic
Convergence.
600,000 14 16 ......................
NL
NC
Pelagic .................
Vagrant ........
NA .....................................
NL
NC
Killer whale (Orcinus orca)
Pelagic, shelf,
coastal, pack
ice.
Pelagic, shelf,
coastal.
Pelagic, shelf,
coastal.
Common ......
Anti-tropical in Northern
and Southern Hemisphere.
Cosmopolitan ....................
80,000 3—South of Antarctic Convergence.
NL
NC
NL
NC
NL
NC
Pelagic, shelf,
coastal.
Uncommon ..
NL
NC
Pelagic, shelf,
coastal.
Coastal, shelf, offshore.
Shelf, slope ..........
Vagrant .......
NL
NC
NL, *C
NC
Common ......
Temperate waters—Southern Hemisphere.
NL
NC
Pelagic .................
Vagrant ........
NC
Rare ............
289,000 3—Eastern Tropical Pacific Ocean.
7,400 17 .............................
NL
Nearshore ............
Pantropical—30° North to
30° South.
Shallow coastal waters—
New Zealand (Maui’s
dolpin—west North Island).
C
NC
Pelagic, ice edge
Uncommon ..
33° South to pack ice .......
NL
NC
Coastal, shelf,
slope.
Mainly nearshore
Vagrant ........
NL
NC
NL
NC
Off continental
shelf, convergence zones,
upwelling.
Slope, Pelagic ......
Vagrant .......
Circumglobal—40° North
to 40° South.
Circumglobal—40° North
to 40° South.
Circumglobal—50 to 40
South.
144,000 3 to 150,000 14—
South of Antarctic Convergence.
At least 2,000,000 3—
Worldwide.
At least 1,200,000 3—
Worldwide.
At least 1,100,000 3—
Worldwide.
NL
NC
NL
NC
Pelagic .................
Vagrant ........
NL
NC
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False killer whale
(Pseudorca crassidens).
Long-finned pilot whale
(Globicephala melas).
Short-finned pilot whale
(Globicephala
macrocephalus).
Melon-headed whale
(Peponocephala electra).
Bottlenose dolphin
(Tursiops truncatus).
Dusky dolphin
(Lagenorhynchus
obscurus).
Fraser’s dolphin
(Lagenodelphis hosei).
Hector’s dolphin
(Cephalorhynchus
hectori; including Maui’s
dolphin subspecies [C. h.
maui]).
Hourglass dolphin
(Lagenorhynchus
cruciger).
Pantropical spotted dolphin
(Stenella attenuata).
Spinner dolphin (Stenella
longirostris).
Striped dolphin (Stenella
coeruleoalba).
Risso’s dolphin (Grampus
griseus).
Rough-toothed dolphin
(Steno bredanensis).
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Uncommon ..
Common ......
Common ......
Vagrant .......
Vagrant ........
PO 00000
Frm 00010
28° North to 30° South in
Pacific Ocean.
Circumantarctic .................
Circumglobal—tropical and NA .....................................
warmer temperate water.
Circumpolar—19 to 68°
200,000 3 5 14—South of
South in Southern
Antarctic Convergence.
Hemisphere.
Circumglobal—50° North
At least 600,000 3—Worldto 40° South.
wide.
Circumglocal—40° North
to 35° South.
45° North to 45° South .....
Circumglobal—Tropical
and Temperate waters.
Circumglobal—40° North
to 35° South.
Fmt 4701
Sfmt 4703
45,000 3—Eastern Tropical
Pacific Ocean.
At least 614,000 3—Worldwide.
12,000 to 20,000 17—New
Zealand.
At least 330,000 3—Worldwide.
NA .....................................
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ESA 1
MMPA 2
Species
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TABLE 3—THE HABITAT, OCCURRENCE, RANGE, REGIONAL ABUNDANCE, AND CONSERVATION STATUS OF MARINE MAMMALS THAT MAY OCCUR IN OR NEAR THE PROPOSED LOW-ENERGY SEISMIC SURVEY AREA IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND—Continued
[See text and tables 2 in SIO’s IHA application for further details]
ESA 1
MMPA 2
Species
Habitat
Occurrence
Range
Population estimate
Short-beaked common dolphin (Delphinus delphis).
Southern right whale dolphin (Lissodelphis
peronii).
Spectacled porpoise
(Phocoena dioptrica).
Pelagic .................
Common ......
NC
Uncommon ..
At least 3,500,000 3—
Worldwide.
NA .....................................
NL
Pelagic .................
Circumglobal—tropical and
warm temperate waters.
12 to 65° South ................
NL
NC
Coastal, pelagic ...
Vagrant ........
Circumpolar—Southern
Hemisphere.
NA .....................................
NL
NC
5,000,000 to
15,000,000 3 6—Worldwide.
220,000 to 440,000 3 7—
Worldwide.
130,000 3 20,000 to
220,000 11—Worldwide.
NL
NC
NL
NC
NL
NC
Pinnipeds
Crabeater seal (Lobodon
carcinophaga).
Coastal, pack ice
Vagrant .......
Circumpolar—Antarctic .....
Pack ice, sub-Antarctic islands.
Pack ice, smooth
ice floes, pelagic.
Weddell seal
Fast ice, pack ice,
(Leptonychotes weddellii).
sub-Antarctic islands.
Southern elephant seal
Coastal, pelagic,
(Mirounga leonina).
sub-Antarctic
waters.
Vagrant .......
Sub-Antarctic islands to
pack ice.
Circumpolar—Antarctic .....
Antarctic fur seal
(Arctocephalus gazella).
New Zealand fur seal
(Arctocephalus forsteri).
Leopard seal (Hydrurga
leptonyx).
Ross seal (Ommatophoca
rossii).
Vagrant .......
Vagrant ........
Circumpolar—Southern
Hemisphere.
500,000 to 1,000,000 3 8—
Worldwide.
NL
NC
Uncommon ..
Circumpolar—Antarctic
Convergence to pack
ice.
NL
NC
Shelf, rocky habitats.
Rocky habitats,
sub-Antarctic islands.
Subantarctic fur seal
Shelf, rocky habi(Arctocephalus tropicalis).
tats.
Vagrant ........
NL
NC
NL
NC
NL
NC
New Zealand sea lion
(Phocarctos hookeri).
Rare ............
Sub-Antarctic islands to
pack ice edge.
North and South Islands,
New Zealand Southern
and Western Australia.
Subtropical front to subAntarctic islands and
Antarctica.
Sub-Antarctic islands
south of New Zealand.
640,000 9 to 650,000 3—
Worldwide 470,000—
South Georgia Island 11
607,000 17.
1,600,000 10 to
3,000,000 3—Worldwide.
135,000 3—Worldwide
50,000 to 100,000 18—
New Zealand.
Greater than 310,000 3—
Worldwide.
NL
NC
Shelf, rocky habitats.
Common ......
Vagrant ........
12,500 3 .............................
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NA = Not available or not assessed.
* Fjordland population.
1 U.S. Endangered Species Act: EN = Endangered, T = Threatened, DL = Delisted, NL = Not listed, C = Candidate.
2 U.S. Marine Mammal Protection Act: D = Depleted, S = Strategic, NC = Not Classified.
3 Jefferson et al., 2008.
4 Kenney, 2009.
5 Olson, 2009.
6 Bengston, 2009.
7 Rogers, 2009.
8 Thomas and Terhune, 2009.
9 Hindell and Perrin, 2009.
10 Arnould, 2009.
11 Academic Press, 2009.
12 IWC, 2014.
13 IWC, 1981.
14 Boyd, 2002.
15 Dwarf and Antarctic minke whale combined.
16 All Antarctic beaked whales combined.
17 New Zealand Department of Conservation.
18 Suisted and Neale, 2004.
Refer to sections 3 and 4 of SIO’s IHA
application for detailed information
regarding the abundance and
distribution, population status, and life
history and behavior of these marine
mammal species and their occurrence in
the proposed action area. The IHA
application also presents how SIO
calculated the estimated densities for
the marine mammals in the proposed
study area. NMFS has reviewed these
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data and determined them to be the best
available scientific information for the
purposes of the proposed IHA.
Potential Effects of the Proposed
Specified Activity on Marine Mammals
This section includes a summary and
discussion of the ways that the types of
stressors associated with the specified
activity (e.g., seismic airgun operation,
vessel movement, and gear deployment)
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have been thought to impact marine
mammals. This discussion may also
include reactions that we consider to
rise to the level of a take and those that
we do not consider to rise to the level
of take (for example, with acoustics, we
may include a discussion of studies that
showed animals not reacting at all to
sound or exhibiting barely measureable
avoidance). This section is intended as
a background of potential effects and
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does not consider either the specific
manner in which this activity would be
carried out or the mitigation that would
be implemented, and how either of
those would shape the anticipated
impacts from this specific activity. The
‘‘Estimated Take by Incidental
Harassment’’ section later in this
document would include a quantitative
analysis of the number of individuals
that are expected to be taken by this
activity. The ‘‘Negligible Impact
Analysis’’ section will include the
analysis of how this specific activity
will impact marine mammals and will
consider the content of this section, the
‘‘Estimated Take by Incidental
Harassment’’ section, the ‘‘Proposed
Mitigation’’ section, and the
‘‘Anticipated Effects on Marine Mammal
Habitat’’ section to draw conclusions
regarding the likely impacts of this
activity on the reproductive success or
survivorship of individuals and from
that on the affected marine mammal
populations or stocks.
When considering the influence of
various kinds of sound on the marine
environment, it is necessary to
understand that different kinds of
marine life are sensitive to different
frequencies of sound. Based on available
behavioral data, audiograms have been
derived using auditory evoked
potentials, anatomical modeling, and
other data, Southall et al. (2007)
designate ‘‘functional hearing groups’’
for marine mammals and estimate the
lower and upper frequencies of
functional hearing of the groups. The
functional groups and the associated
frequencies are indicated below (though
animals are less sensitive to sounds at
the outer edge of their functional range
and most sensitive to sounds of
frequencies within a smaller range
somewhere in the middle of their
functional hearing range):
• Low-frequency cetaceans (13
species of mysticetes): Functional
hearing is estimated to occur between
approximately 7 Hz and 30 kHz;
• Mid-frequency cetaceans (32
species of dolphins, six species of larger
toothed whales, and 19 species of
beaked and bottlenose whales):
Functional hearing is estimated to occur
between approximately 150 Hz and 160
kHz;
• High-frequency cetaceans (eight
species of true porpoises, six species of
river dolphins, Kogia spp., the
franciscana [Pontoporia blainvillei], and
four species of cephalorhynchids):
Functional hearing is estimated to occur
between approximately 200 Hz and 180
kHz; and
• Phocid pinnipeds in water:
Functional hearing is estimated to occur
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between approximately 75 Hz and 100
kHz;
• Otariid pinnipeds in water:
Functional hearing is estimated to occur
between approximately 100 Hz and 40
kHz.
As mentioned previously in this
document, 32 marine mammal species
(30 cetacean and 2 pinniped species) are
likely to occur in the proposed lowenergy seismic survey area. Of the 30
cetacean species likely to occur in SIO’s
proposed action area, 9 are classified as
low-frequency cetaceans (southern right,
pygmy right, humpback, minke,
Antarctic minke, Bryde’s, sei, fin, and
blue whale), 20 are classified as midfrequency cetaceans (sperm, Cuvier’s
beaked, Shepherd’s beaked, southern
bottlenose, Andrew’s beaked,
Blainville’s beaked, Gray’s beaked,
Hector’s beaked, spade-toothed beaked,
strap-toothed beaked, killer, false killer,
long-finned pilot, and short-finned pilot
whale, and bottlenose, dusky, Hector’s,
hourglass, short-beaked common, and
southern right whale dolphin), and 1 is
classified as high-frequency cetaceans
(pygmy sperm whale) (Southall et al.,
2007). Of the 2 pinniped species likely
to occur in SIO’s proposed action area,
1 is classified as phocid (southern
elephant seal) and 1 is classified as
otariid (New Zealand fur seal) (Southall
et al., 2007). A species functional
hearing group is a consideration when
we analyze the effects of exposure to
sound on marine mammals.
Acoustic stimuli generated by the
operation of the airguns, which
introduce sound into the marine
environment, have the potential to
cause Level B harassment of marine
mammals in the proposed study 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 hearing
impairment, or non-auditory physical or
physiological effects (Richardson et al.,
1995; Gordon et al., 2004; Nowacek et
al., 2007; Southall et al., 2007).
Permanent hearing impairment, in the
unlikely event that it occurred, would
constitute injury, but temporary
threshold shift (TTS) is not an injury
(Southall et al., 2007; Le Prell, 2012).
Although the possibility cannot be
entirely excluded, it is unlikely that the
proposed project would result in any
cases of temporary or permanent
hearing impairment, or any significant
non-auditory physical or physiological
effects. Based on the available data and
studies described here, some behavioral
disturbance is expected. A more
comprehensive review of these issues
can be found in the NSF/USGS PEIS
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(2011) and L–DEO’s ‘‘Final
Environmental Assessment of a Marine
Geophysical Survey by the R/V Marcus
G. Langseth in the Atlantic Ocean off
Cape Hatteras, September to October
2014.’’
Tolerance
Richardson et al. (1995) defines
tolerance as the occurrence of marine
mammals in areas where they are
exposed to human activities or manmade noise. In many cases, tolerance
develops by the animal habituating to
the stimulus (i.e., the gradual waning of
responses to a repeated or ongoing
stimulus) (Richardson et al., 1995;
Thorpe, 1963), but because of ecological
or physiological requirements, many
marine animals may need to remain in
areas where they are exposed to chronic
stimuli (Richardson et al., 1995).
Numerous studies have shown that
pulsed sounds from airguns are often
readily detectable in the water at
distances of many kilometers (Nieukirk
et al., 2012). 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. 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).
The airguns for the proposed lowenergy seismic survey have dominant
frequency components of 0 to 188 Hz.
This frequency range fully overlaps the
lower part of the frequency range of
odontocete calls and/or functional
hearing (full range about 150 Hz to 180
kHz). Airguns also produce a small
portion of their sound at mid and high
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frequencies that overlap most, if not all,
frequencies produced by odontocetes.
While it is assumed that mysticetes can
detect acoustic impulses from airguns
and vessel sounds (Richardson et al.,
1995a), sub-bottom profilers, and most
of the multi-beam echosounders would
likely be detectable by some mysticetes
based on presumed mysticete hearing
sensitivity. Odontocetes are presumably
more sensitive to mid to high
frequencies produced by the multi-beam
echosounders and sub-bottom profilers
than to the dominant low frequencies
produced by the airguns and vessel. A
more comprehensive review of the
relevant background information for
odontocetes appears in Section 3.6.4.3,
Section 3.7.4.3 and Appendix E of the
NSF/USGS PEIS (2011).
Masking effects of pulsed sounds
(even from large arrays of airguns) on
marine mammal calls and other natural
sounds are expected to be limited.
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.
Situations with prolonged strong
reverberation are infrequent. However,
it is common for reverberation to cause
some lesser degree of elevation of the
background level between airgun pulses
(Gedamke, 2011; Guerra et al., 2011,
2013), and this weaker reverberation
presumably reduces the detection range
of calls and other natural sound to some
degree. Guerra et al. (2013) reported that
ambient noise levels between seismic
pulses were elevated because of
reverberation at ranges of 50 km (27
nmi) from the seismic source. Based on
measurements in deep water of the
Southern Ocean, Gedamke (2011)
estimated that the slight elevation of
background levels during intervals
between pulses reduced blue and fin
whale communication space by as much
as 36 to 51% when a seismic survey was
operating 450 to 2,800 km (243 to
1,511.9 nmi) away. Based on
preliminary modeling, Wittekind et al.
(2013) reported that airgun sounds
could reduce the communication range
of blue and fin whales 2,000 km (1,079.9
nmi) from the seismic source. Klinck et
al. (2012) also found reverberation
effects between pulses. Nieukirk et al.
(2012) and Blackwell et al. (2013) noted
the potential for masking effects from
seismic surveys on large whales.
Some baleen and toothed whales are
known to continue calling in the
presence of seismic pulses, and their
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calls can usually be heard between the
seismic pulses (e.g., Richardson et al.,
1986; McDonald et al., 1995; Greene et
al., 1999; Nieukirk et al., 2004, 2012;
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 North Atlantic Ocean went silent
for an extended period starting soon
after the onset of a seismic survey in the
area. Similarly, there has been one
report that sperm whales ceased calling
when exposed to pulses from a very
distant seismic ship (Bowles et al.,
1994). However, more recent studies
found that they continued calling in the
presence of seismic pulses (Madsen et
al., 2002; Tyack et al., 2003; Smultea et
al., 2004; Holst et al., 2006; and Jochens
et al., 2008). Cerchio et al. (2014)
suggested that the breeding display of
humpback whales off Angola could
have been disrupted by seismic sounds,
as singing activity declined with
increasing received levels. In addition,
some cetaceans are known to change
their calling rates, shift their peak
frequencies, or otherwise modify their
vocal behavior in response to airgun
sounds (Di Iorio and Clark, 2010;
Castellote et al., 2012; Blackwell et al.,
2013). Di Iorio and Clark (2009) found
evidence of increased calling by blue
whales during operations by a lowerenergy seismic source (i.e., sparker). The
hearing systems of baleen whales are
undoubtedly more sensitive to lowfrequency sounds than are the ears of
small odontocetes that have been
studied directly (MacGillivary et al.,
2013). Dolphins and porpoises
commonly are heard calling while
airguns are operating (e.g., Gordon et al.,
2004; Smultea et al., 2004; Holst et al.,
2005a, b; and Potter et al., 2007). The
sounds important to small odontocetes
are predominantly at much higher
frequencies than are the dominant
components of airgun sounds, thus
limiting the potential for masking.
Pinnipeds have the most sensitive
hearing and/or produce most of their
sounds in frequencies higher than the
dominant components of airgun sound,
but there is some overlap in the
frequencies of the airgun pulses and the
calls. However, the intermittent nature
of airgun pules presumably reduces 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 (Di
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15071
Iorio and Clark, 2009). The North
Atlantic right whales (Eubalaena
glacialis) 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,
NMFS expects the masking effects of
seismic pulses to 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; Ellison et al., 2012). 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 (New et al., 2013). 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);
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• 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 sound. In most cases, this
approach likely overestimates the
numbers of marine mammals that would
be affected in some biologicallyimportant manner.
Baleen Whales—Baleen whales
generally tend to avoid operating
airguns, but avoidance radii are quite
variable (reviewed in Richardson et al.,
1995; Gordon et al., 2004). 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. In the
cases of migrating gray (Eschrichtius
robustus) and bowhead (Balaena
mysticetus) whales, the observed
changes in behavior appeared to be of
little or no biological consequence to the
animals (Richardson et al., 1995). They
simply avoided the sound source by
displacing their migration route to
varying degrees, but within the natural
boundaries of the migration corridors
(Malme et al., 1984; Malme and Miles,
1985; Richardson et al., 1995).
Studies of gray, bowhead, and
humpback whales have shown that
seismic pulses with received levels of
160 to 170 dB re 1 mPa (rms) 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 4 to 15 km (2.2
to 8.1 nmi) 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
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become evident at somewhat lower
received levels, and studies have shown
that some species of baleen whales,
notably bowhead, gray, and humpback
whales, at times, show strong avoidance
at received levels lower than 160 to 170
dB re 1 mPa (rms).
Researchers have studied the
responses of humpback whales to
seismic surveys during migration,
feeding during the summer months,
breeding while offshore from Angola,
and wintering offshore from Brazil.
McCauley et al. (1998, 2000a) studied
the responses of humpback whales off
western Australia to a full-scale seismic
survey with a 16 airgun array (2,678 in3)
and to a single airgun (20 in3) with
source level of 227 dB re 1 mPa (p-p). In
the 1998 study, they documented that
avoidance reactions began at 5 to 8 km
(2.7 to 4.3 nmi) from the array, and that
those reactions kept most pods
approximately 3 to 4 km (1.6 to 2.2 nmi)
from the operating seismic boat. In the
2000 study, they noted localized
displacement during migration of 4 to 5
km (2.2 to 2.7 nmi) by traveling pods
and 7 to 12 km (3.8 to 6.5 nmi) 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 mPa (rms) for
humpback pods containing females, and
at the mean closest point of approach
distance the received level was 143 dB
re 1 mPa (rms). The initial avoidance
response generally occurred at distances
of 5 to 8 km (2.7 to 4.3 nmi) from the
airgun array and 2 km (1.1 nmi) 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 (rms). Studies examining the
behavioral responses of humpback
whales to airguns are currently
underway off eastern Australia (Cato et
al., 2011, 2012, 2013).
Data collected by observers during
several seismic surveys in the
Northwest Atlantic 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 vs. non-seismic periods
(Moulton and Holst, 2010).
Humpback whales on their summer
feeding grounds in southeast Alaska did
not exhibit persistent avoidance when
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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 dB re 1 mPa (rms). 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.
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). The evidence for this was
circumstantial and subject to alternative
explanations (IAGC, 2004). Also, the
evidence was not consistent with
subsequent results from the same area of
Brazil (Parente et al., 2006), or with
direct studies of humpbacks exposed to
seismic surveys in other areas and
seasons. After allowance for data from
subsequent years, there was ‘‘no
observable direct correlation’’ between
strandings and seismic surveys (IWC,
2007: 236).
There are no reactions of right whales
to seismic surveys. However, Rolland et
al. (2012) suggested that ship noise
causes increased stress in right whales;
they showed that baseline levels of
stress-related fecal hormone metabolites
decreased in North Atlantic right whales
with a 6 dB decrease in underwater
noise from vessels. Wright et al. (2011)
also reported that sound could be a
potential source of stress for marine
mammals.
Results from bowhead whales show
that their responsiveness can be quite
variable depending on their activity
(migrating versus feeding). Bowhead
whales migrating west across the
Alaskan Beaufort Sea in autumn, in
particular, are unusually responsive,
with substantial avoidance occurring
out to distances of 20 to 30 km (10.8 to
16.2 nmi) from a medium-sized airgun
source (Miller et al., 1999; Richardson et
al., 1999). However, more recent
research on bowhead whales
corroborates earlier evidence that,
during the summer feeding season,
bowheads are not as sensitive to seismic
sources (Miller et al., 2005).
Nonetheless, Robertson et al. (2013)
showed that bowheads on their summer
feeding grounds showed subtle but
statistically significant changes in
surfacing-respiration-dive cycles during
exposure to seismic sounds, including
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shorter surfacing intervals, shorter
dives, and decreased number of blows
per surface interval.
Bowhead whale calls detected in the
presence and absence of airgun sounds
have been studied extensively in the
Beaufort Sea. Bowheads continue to
produce calls of the usual types when
exposed to airgun sounds on their
summering grounds, although number
of calls detected are significantly lower
in the presence than in the absence of
airgun pulses; Blackwell et al. (2013)
reported that calling rates in 2007
declined significantly where received
SPLs from airgun sounds were 116 to
129 dB re 1 mPa. Thus, bowhead whales
in the Beaufort Sea apparently decrease
their calling rates in response to seismic
operations, although movement out of
the area could also contribute to the
lower call detection rate (Blackwell et
al., 2013).
A multivariate analysis of factors
affecting the distribution of calling
bowhead whales during their fall
migration in 2009 noted that the
southern edge of the distribution of
calling whales was significantly closer
to shore with increasing levels of airgun
sound from a seismic survey a few
hundred kms to the east of the study
area (i.e., behind the westwardmigrating whales; McDonald et al.,
2010, 2011). It was not known whether
this statistical effect represented a
stronger tendency for quieting of the
whales farther offshore in deeper water
upon exposure to airgun sound, or an
actual inshore displacement of whales.
Reactions of migrating and feeding
(but not wintering) gray whales to
seismic surveys have been studied.
Malme et al. (1986, 1988) studied the
responses of feeding eastern Pacific gray
whales to pulses from a single 100 in3
airgun off St. Lawrence Island in the
northern Bering Sea. They estimated,
based on small sample sizes, that 50
percent of feeding gray whales stopped
feeding at an average received pressure
level of 173 dB re 1 mPa on an
(approximate) rms basis, and that 10
percent of feeding whales interrupted
feeding at received levels of 163 dB re
1 mPa (rms). 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).
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Various species of Balaenoptera (blue,
sei, fin, and minke whales) have
occasionally been seen in areas
ensonified by airgun pulses (Stone,
2003; MacLean and Haley, 2004; Stone
and Tasker, 2006), and calls from blue
and fin whales have been localized in
areas with airgun operations (e.g.,
McDonald et al., 1995; Dunn and
Hernandez, 2009; Castellote et al.,
2010). Sightings by observers on seismic
vessels off the United Kingdom from
1997 to 2000 suggest that, during times
of good sightability, sighting rates for
mysticetes (mainly fin and sei whales)
were similar when large arrays of
airguns were shooting versus 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, 2012) reported
that singing fin whales in the
Mediterranean moved away from an
operating airgun array, and their song
notes had low bandwidths during
periods with versus without airgun
sounds.
Ship-based monitoring studies of
baleen whales (including blue, fin, sei,
minke, and humpback whales) in the
Northwest Atlantic found that overall,
this group had lower sighting rates
during seismic vs. non-seismic periods
(Moulton and Holst, 2010). Baleen
whales as a group were also seen
significantly farther from the vessel
during seismic compared with nonseismic 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
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Malme et al., 1984; Richardson et al.,
1995; Allen and Angliss, 2010). The
western Pacific gray whale population
did not seem affected by a seismic
survey in its feeding ground during a
previous year (Johnson et al., 2007).
Similarly, bowhead whales have
continued to travel to the eastern
Beaufort Sea each summer, and their
numbers have increased notably,
despite seismic exploration in their
summer and autumn range for many
years (Richardson et al., 1987; Allen and
Angliss, 2010).
Toothed Whales—Little systematic
information is available about reactions
of toothed whales to noise pulses. Few
studies similar to the more extensive
baleen whale/seismic pulse work
summarized above have been reported
for toothed whales. However, there are
recent systematic studies on sperm
whales (e.g., Gordon et al., 2006;
Madsen et al., 2006; Winsor and Mate,
2006; Jochens et al., 2008; Miller et al.,
2009). There is an increasing amount of
information about responses of various
odontocetes to seismic surveys based on
monitoring studies (e.g., Stone, 2003;
Smultea et al., 2004; Moulton and
Miller, 2005; Bain and Williams, 2006;
Holst et al., 2006; Stone and Tasker,
2006; Potter et al., 2007; Hauser et al.,
2008; Holst and Smultea, 2008; Weir,
2008; Barkaszi et al., 2009; Richardson
et al., 2009; Moulton and Holst, 2010).
Seismic operators and PSOs on
seismic vessels regularly see dolphins
and other small toothed whales near
operating airgun arrays, but in general
there is a tendency for most delphinids
to show some avoidance of operating
seismic vessels (e.g., Goold, 1996a,b,c;
Calambokidis and Osmek, 1998; Stone,
2003; Moulton and Miller, 2005; Holst
et al., 2006; Stone and Tasker, 2006;
Weir, 2008; Richardson et al., 2009;
Barkaszi et al., 2009; Moulton and
Holst, 2010; Barry et al., 2012). 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
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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.
Preliminary findings of a monitoring
study of narwhals (Monodon
monoceros) in Melville Bay, Greenland
(summer and fall 2012) showed no
short-term effects of seismic survey
activity on narwhal distribution,
abundance, migration timing, and
feeding habits (Heide-Jorgensen et al.,
2013a). In addition, there were no
reported effects on narwhal hunting.
These findings do not seemingly
support a suggestion by Heide-Jorgensen
et al. (2013b) that seismic surveys in
Baffin Bay may have delayed the
migration timing of narwhals, thereby
increasing the risk of narwhals to ice
entrapment.
Results of 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 (Phocoenoides dalli) (Stone,
2003; MacLean and Koski, 2005; Bain
and Williams, 2006; Stone and Tasker,
2006). Thompson et al. (2013) reported
decreased densities and reduced
acoustic detections of harbor porpoise
in response to a seismic survey in
Moray Firth, Scotland, at ranges of 5 to
10 km (2.7 to 5.4 nmi) (SPLs of 165 to
172 dB re 1 mPa; sound exposure levels
(SELs) of 145 to 151 dB mPa2s); however,
animals returned to the area within a
few hours. Dall’s porpoises seem
relatively tolerant of airgun operations
(MacLean and Koski, 2005; Bain and
Williams, 2006), although they too have
been observed to avoid large arrays of
operating airguns (Calambokidis and
Osmek, 1998; Bain and Williams, 2006).
This apparent difference in
responsiveness of these two porpoise
species is consistent with their relative
responsiveness to boat traffic and some
other acoustic sources (Richardson et
al., 1995; Southall et al., 2007).
Most studies of sperm whales exposed
to airgun sounds indicate that the sperm
whale shows considerable tolerance of
airgun pulses (e.g., Stone, 2003;
Moulton et al., 2005, 2006a; Stone and
Tasker, 2006; Weir, 2008). In most cases
the whales do not show strong
avoidance, and they continue to call.
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.
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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 may be reduced by close
approach of vessels. In any event, it is
likely that most beaked whales would
also show strong avoidance of an
approaching seismic vessel, although
this has not been documented
explicitly. In fact, Moulton and Holst
(2010) reported 15 sightings of beaked
whales during seismic studies in the
Northwest Atlantic; seven of those
sightings were made at times when at
least one airgun was operating. There
was little evidence to indicate that
beaked whale behavior was affected by
airgun operations; sighting rates and
distances were similar during seismic
and non-seismic periods (Moulton and
Holst, 2010).
There are increasing indications that
some beaked whales tend to strand
when naval exercises involving midfrequency sonar operation are ongoing
nearby (e.g., Simmonds and LopezJurado, 1991; Frantzis, 1998; NOAA and
USN, 2001; Jepson et al., 2003;
Hildebrand, 2005; Barlow and Gisiner,
2006; see also the ‘‘Stranding and
Mortality’’ section in this notice). These
strandings are apparently a disturbance
response, although auditory or other
injuries or other physiological effects
may also be involved. Whether beaked
whales would ever react similarly to
seismic surveys is unknown. Seismic
survey sounds are quite different from
those of the sonar in operation during
the above-cited incidents.
Odontocete reactions to large arrays of
airguns are variable and, at least for
delphinids, seem to be confined to a
smaller radius than has been observed
for the more responsive of some
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
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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).
Pinnipeds—Pinnipeds are not likely
to show a strong avoidance reaction to
the airgun array. Visual monitoring from
seismic vessels has shown only slight (if
any) avoidance of airguns by pinnipeds,
and only slight (if any) changes in
behavior. In the Beaufort Sea, some
ringed seals avoided an area of 100 m
to (at most) a few hundred meters
around seismic vessels, but many seals
remained within 100 to 200 m (328 to
656 ft) of the trackline as the operating
airgun array passed by (e.g., Harris et al.,
2001; Moulton and Lawson, 2002;
Miller et al., 2005.). Ringed seal (Pusa
hispida) sightings averaged somewhat
farther away from the seismic vessel
when the airguns were operating than
when they were not, but the difference
was small (Moulton and Lawson, 2002).
Similarly, in Puget Sound, sighting
distances for harbor seals (Phoca
vitulina) and California sea lions
(Zalophus californianus) tended to be
larger when airguns were operating
(Calambokidis and Osmek, 1998).
Previous telemetry work suggests that
avoidance and other behavioral
reactions by two other species of seals
to small airgun sources may be stronger
than evident to date from visual studies
of pinnipeds reactions to airguns
(Thompson et al., 1998).
During seismic exploration off Nova
Scotia, gray seals (Halichoerus grypus)
exposed to noise from airguns and
linear explosive charges did not react
strongly (J. Parsons in Greene et al.,
1985). Pinnipeds in both water and air,
sometimes tolerate strong noise pulses
from non-explosive and explosive
scaring devices, especially if attracted to
the area for feeding and reproduction
(Mate and Harvey, 1987; Reeves et al.,
1996). Thus pinnipeds are expected to
be rather tolerant of, or habituate to,
repeated underwater sounds from
distant seismic sources, at least when
the animals are strongly attracted to the
area.
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, Carder, Schlundt, and
Ridgway, 2005). Factors that influence
the amount of threshold shift include
the amplitude, duration, frequency
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content, temporal pattern, and energy
distribution of noise exposure. The
magnitude of hearing threshold shift
normally decreases over time following
cessation of the noise exposure. The
amount of threshold shift just after
exposure is called the initial threshold
shift. If the threshold shift eventually
returns to zero (i.e., the threshold
returns to the pre-exposure value), it is
called temporary threshold shift (TTS)
(Southall et al., 2007). Researchers have
studied TTS in certain captive
odontocetes and pinnipeds exposed to
strong sounds (reviewed in Southall et
al., 2007). However, there has been no
specific documentation of TTS, let alone
permanent hearing damage, i.e.,
permanent threshold shift (PTS), in freeranging marine mammals exposed to
sequences of airgun pulses during
realistic field conditions.
Temporary Threshold Shift—TTS is
the mildest form of hearing impairment
that can occur during exposure to a
strong sound (Kryter, 1985). While
experiencing TTS, the hearing threshold
rises and a sound must be stronger in
order to be heard. At least in terrestrial
mammals, TTS can last from minutes or
hours to (in cases of strong TTS) days.
For sound exposures at or somewhat
above the TTS threshold, hearing
sensitivity in both terrestrial and marine
mammals recovers rapidly after
exposure to the noise ends. Few data on
sound levels and durations necessary to
elicit mild TTS have been obtained for
marine mammals, and none of the
published data concern TTS elicited by
exposure to multiple pulses of sound.
Available data on TTS in marine
mammals are summarized in Southall et
al. (2007). Table 2 (above) presents the
estimated distances from the Revelle’s
airguns at which the received energy
level (per pulse, flat-weighted) would be
expected to be greater than or equal to
180 and 190 dB re 1 mPa (rms).
The established 180 and 190 dB (rms)
criteria are not considered to be the
levels above which TTS might occur.
Rather, they are the received levels
above which, in the view of a panel of
bioacoustics specialists convened by
NMFS before TTS 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. NMFS also assumes that
cetaceans and pinnipeds exposed to
levels exceeding 160 dB re 1 mPa (rms)
may experience Level B harassment.
For toothed whales, researchers have
derived TTS information for
odontocetes from studies on the
bottlenose dolphin and beluga. The
experiments show that exposure to a
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single impulse at a received level of 207
kPa (or 30 psi, peak-to-peak), which is
equivalent to 228 dB re 1 Pa (peak-topeak), resulted in a 7 and 6 dB TTS in
the beluga whale at 0.4 and 30 kHz,
respectively. Thresholds returned to
within 2 dB of the pre-exposure level
within 4 minutes of the exposure
(Finneran et al., 2002). For the one
harbor porpoise tested, the received
level of airgun sound that elicited onset
of TTS was lower (Lucke et al., 2009).
If these results from a single animal are
representative, it is inappropriate to
assume that onset of TTS occurs at
similar received levels in all
odontocetes (cf. Southall et al., 2007).
Some cetaceans apparently can incur
TTS at considerably lower sound
exposures than are necessary to elicit
TTS in the beluga or bottlenose dolphin.
For baleen whales, there are no data,
direct or indirect, on levels or properties
of sound that are required to induce
TTS. The frequencies to which baleen
whales are most sensitive are assumed
to be lower than those to which
odontocetes are most sensitive, and
natural background noise levels at those
low frequencies tend to be higher. As a
result, auditory thresholds of baleen
whales within their frequency band of
best hearing are believed to be higher
(less sensitive) than are those of
odontocetes at their best frequencies
(Clark and Ellison, 2004). From this, it
is suspected that received levels causing
TTS onset may also be higher in baleen
whales than those of odontocetes
(Southall et al., 2007).
In pinnipeds, researchers have not
measured TTS thresholds associated
with exposure to brief pulses (single or
multiple) of underwater sound. Initial
evidence from more prolonged (nonpulse) exposures suggested that some
pinnipeds (harbor seals in particular)
incur TTS at somewhat lower received
levels than do small odontocetes
exposed for similar durations (Kastak et
al., 1999, 2005; Ketten et al., 2001). The
TTS threshold for pulsed sounds has
been indirectly estimated as being an
SEL of approximately 171 dB re 1 mPa2·s
(Southall et al., 2007) which would be
equivalent to a single pulse with a
received level of approximately 181 to
186 dB re 1 mPa (rms), or a series of
pulses for which the highest rms values
are a few dB lower. Corresponding
values for California sea lions and
northern elephant seals (Mirounga
angustirostris) are likely to be higher
(Kastak et al., 2005).
Additional data are needed to
determine the received levels at which
small odontocetes would start to incur
TTS upon exposure to repeated, lowfrequency pulses of airgun sounds with
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15075
variable received levels. To determine
how close an airgun array would need
to approach in order to elicit TTS, one
would (as a minimum) need to allow for
the sequence of distances at which
airgun pulses would occur, and for the
dependence of received SEL on distance
in the region of the airgun operation
(Breitzke and Bohlen, 2010; Laws,
2012). At the present state of
knowledge, it can be assumed that the
effect is directly related to total receive
energy, although there is recent
evidence that auditory effects in a given
animal are not a simple function of
received acoustic energy. Frequency,
duration of the exposure and occurrence
of gaps within the exposure can also
influence the auditory effect (Finneran
and Schlundt, 2010, 2011, 2013;
Finneran et al., 2010a,b; Finneran 2012;
Ketten, 2012; Kastelein et al., 2013a).
The assumption that, in marine
mammals, the occurrence and
magnitude of TTS is a function of
cumulative acoustic energy (SEL) is
probably an oversimplification
(Finneran, 2012). Popov et al. (2011)
examined the effects of fatiguing noise
on the hearing threshold of Yangtze
finless porpoises (Neophocaena
phocaenoides) when exposed to
frequencies of 32 to 128 kHz at 140 to
160 dB re 1 mPa for 1 to 30 minutes.
They found that an exposure of higher
level and shorter duration produced a
higher TTS than an exposure of equal
SEL but of lower level and longer
duration. Kastelein et al. (2012a,b;
2013b) also reported that the equalenergy model is not valid for predicting
TTS in harbor porpoises or harbor seals.
Recent data have shown that the SEL
required for TTS onset to occur
increases with intermittent exposures,
with some auditory recovery during
silent periods between (Finneran et al.,
2010b; Finneran and Schlundt, 2011).
Schlundt et al. (2013) reported that the
potential for seismic surveys using
airguns to cause auditory effects on
dolphins could be lower than
previously thought. Based on behavioral
tests, Finneran et al. (2011) and
Schlundt et al. (2013) reported no
measurable TTS in bottlenose dolphins
after exposure to 10 impulses from a
seismic airgun with a cumulative SEL of
approximately 195 dB re 1 mPa2s; results
from auditory evoked potential
measurements were more variable
(Schlundt et al., 2013).
Recent studies have also shown that
the SEL necessary to elicit TTS can
depend substantially on frequency, with
susceptibility to TTS increasing with
increasing frequency above 3 kHz
(Finneran and Schlundt, 2010, 2011;
Finneran, 2012). When beluga whales
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were exposed to fatiguing noise with
sound levels of 165 dB re 1 mPa for
durations of 1 to 30 minutes at
frequencies of 11.2 to 90 kHz, the
highest TTS with the longest recovery
time was produced by lower frequencies
(11.2 and 22.5 kHz); TTS effects also
gradually increased with prolonged
exposure time (Popov et al., 2013a).
Popov et al. (2013b) also reported that
TTS produced by exposure to a
fatiguing noise was larger during the
¨
first session (or naıve subject state) with
a beluga whale than TTS that resulted
from the same sound in subsequent
sessions (experienced subject state).
Therefore, Supin et al. (2013) reported
that SEL may not be a valid metric for
examining fatiguing sounds on beluga
whales. Similarly, Nachtigall and Supin
(2013) reported that false killer whales
are able to change their hearing
sensation levels when exposed to loud
sounds, such as warning signals or
echolocation sounds.
It is inappropriate to assume that
onset of TTS occurs at similar received
levels in all cetaceans (Southall et al.,
2007). Some cetaceans could incur TTS
at lower sound exposures than are
necessary to elicit TTS in the beluga or
bottlenose dolphin. Based on the best
available information, Southall et al.
(2007) recommended a TTS threshold
for exposure to a single or multiple
pulses of 183 dB re 1 mPa2s. Tougaard
et al. (2013) proposed a TTS criterion of
165 dB re 1 mPa2s for porpoises based
on data from two recent studies.
Gedamke et al. (2011), based on
preliminary simulation modeling that
attempted to allow for various
uncertainties in assumptions and
variability around population means,
suggested that some baleen whales
whose closest point of approach to a
seismic vessel is 1 km or more could
experience TTS.
Permanent Threshold Shift—When
PTS occurs, there is physical damage to
the sound receptors in the ear. In severe
cases, there can be total or partial
deafness, whereas in other cases, the
animal has an impaired ability to hear
sounds in specific frequency ranges
(Kryter, 1985). There is no specific
evidence that exposure to pulses of
airgun sound can cause PTS in any
marine mammal, even with large arrays
of airguns. However, given the
possibility that mammals close to an
airgun array might incur at least mild
TTS, there has been further speculation
about the possibility that some
individuals occurring very close to
airguns might incur PTS (e.g.,
Richardson et al., 1995, p. 372ff;
Gedamke et al., 2008). Single or
occasional occurrences of mild TTS are
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not indicative of permanent auditory
damage, but repeated or (in some cases)
single exposures to a level well above
that causing TTS onset might elicit PTS.
Relationships between TTS and PTS
thresholds have not been studied in
marine mammals but are assumed to be
similar to those in humans and other
terrestrial mammals (Southall et al.,
2007). PTS might occur at a received
sound level at least several dBs above
that inducing mild TTS if the animal
were exposed to strong sound pulses
with rapid rise times. Based on data
from terrestrial mammals, a
precautionary assumption is that the
PTS threshold for impulse sounds (such
as airgun pulses as received close to the
source) is at least 6 dB higher than the
TTS threshold on a peak-pressure basis,
and probably greater than 6 dB (Southall
et al., 2007). Given the higher level of
sound necessary to cause PTS as
compared with TTS, it is considerably
less likely that PTS would occur. Baleen
whales generally avoid the immediate
area around operating seismic vessels,
as do some other marine mammals.
Non-auditory Physiological Effects—
Non-auditory physiological effects or
injuries that theoretically might occur in
marine mammals exposed to strong
underwater sound include stress,
neurological effects, bubble formation,
resonance, and other types of organ or
tissue damage (Cox et al., 2006; Southall
et al., 2007). Studies examining such
effects are limited. However, resonance
effects (Gentry, 2002) and direct noiseinduced bubble formations (Crum et al.,
2005) are implausible in the case of
exposure to an impulsive broadband
source like an airgun array. If seismic
surveys disrupt diving patterns of deepdiving species, this might perhaps result
in bubble formation and a form of the
bends, as speculated to occur in beaked
whales exposed to sonar. However,
there is no specific evidence of this
upon exposure to airgun pulses.
In general, very little is known about
the potential for seismic survey sounds
(or other types of strong underwater
sounds) to cause non-auditory physical
effects in marine mammals. Such
effects, if they occur at all, would
presumably be limited to short distances
and to activities that extend over a
prolonged period. The available data do
not allow identification of a specific
exposure level above which nonauditory effects can be expected
(Southall et al., 2007), or any
meaningful quantitative predictions of
the numbers (if any) of marine mammals
that might be affected in those ways.
Marine mammals that show behavioral
avoidance of seismic vessels, including
most baleen whales, some odontocetes,
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and some pinnipeds, are especially
unlikely to incur non-auditory physical
effects.
There is no definitive evidence that
any of these effects occur even for
marine mammals in close proximity to
large airgun arrays. However, Gray and
Van Waerebeek (2011) have suggested a
cause-effect relationship between a
seismic survey off Liberia in 2009 and
the erratic movement, postural
instability, and akinesia in a pantropical
spotted dolphin based on spatially and
temporally close association with the
airgun array. Additionally, 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 (Castellote and Llorens,
2013).
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
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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—The proposed action is
not a military readiness activity or using
military active sonar (non-pulse).
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 mid1980s 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
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
(non-pulse sound) and, in one case, the
regional co-occurrence of an L–DEO
seismic survey (Malakoff, 2002; Cox et
al., 2006), has raised the possibility that
beaked whales exposed to strong
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‘‘pulsed’’ sounds could also be
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 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. The evidence for this
remains circumstantial and associated
with exposure to naval mid-frequency
sonar, not seismic surveys (Cox et al.,
2006; Southall et al., 2007).
Seismic pulses and mid-frequency
sonar signals are quite different, and
some mechanisms by which sonar
sounds have been hypothesized to affect
beaked whales are unlikely to apply to
airgun pulses. Sounds produced by
airgun arrays are broadband impulses
with most of the energy below one kHz.
Typical military mid-frequency sonar
emits non-impulse sounds at
frequencies of 2 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
expect that the same effects to marine
mammals would result from military
sonar and seismic surveys. However,
evidence that sonar signals can, in
special circumstances, lead (at least
indirectly) to physical damage and
mortality (e.g., Balcomb and Claridge,
2001; NOAA and USN, 2001; Jepson et
´
al., 2003; Fernandez et al., 2004, 2005;
Hildebrand 2005; Cox et al., 2006)
suggests that caution is warranted when
dealing with exposure of marine
mammals to any high-intensity sound.
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There is no conclusive evidence of
cetacean strandings or deaths at sea as
a result of exposure to seismic surveys,
but a few cases of strandings in the
general area where a seismic survey was
ongoing have led to speculation
concerning a possible link between
seismic surveys and strandings.
Suggestions that there was a link
between seismic surveys and strandings
of humpback whales in Brazil (Engel et
al., 2004) were not well founded (IAGC,
2004; IWC, 2007). In September 2002,
there was a stranding of two Cuvier’s
beaked whales in the Gulf of California,
Mexico, when the L–DEO vessel R/V
Maurice Ewing was operating a 20
airgun (8,490 in3) array in the general
region. The link between the stranding
and the seismic surveys was
inconclusive and not based on any
physical evidence (Hogarth, 2002;
Yoder, 2002). Nonetheless, the Gulf of
California incident plus the beaked
whale strandings near naval exercises
involving use of mid-frequency sonar
suggests a need for caution in
conducting seismic surveys in areas
occupied by beaked whales until more
is known about effects of seismic
surveys on those species (Hildebrand,
2005). No injuries of beaked whales are
anticipated during the proposed study
because of:
(1) The high 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 to be used in the proposed
study and operated by SIO and those
involved in the naval exercises
associated with strandings.
Potential Effects of Other Acoustic
Devices and Sources
Multi-Beam Echosounder
SIO would operate the Kongsberg EM
122 multi-beam echosounder from the
source vessel during the planned study.
Sounds from the multi-beam
echosounder are very short pulses,
occurring for approximately 2 to 15 ms
once every 5 to 20 seconds, depending
on water depth. Most of the energy in
the sound pulses emitted by the multibeam echosounder is at frequencies near
12 kHz (10.5 to 13), and the maximum
source level is 242 dB re 1 mPa (rms).
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
(in water less than 1,000 m) consecutive
successive fan-shaped transmissions
(segments) at different cross-track
angles. Any given marine mammal at
depth near the trackline would be in the
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main beam for only one or two of the
eight 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 would receive
only limited amounts of pulse energy
because of the short pulses. Animals
close to the ship (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 a multi-beam 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 TTS.
Navy sonars that have been linked to
avoidance reactions and stranding of
cetaceans: (1) Generally have longer
pulse duration than the Kongsberg EM
122; and (2) are often directed close to
horizontally, as well as omnidirectional,
versus more downward and narrowly
for the multi-beam echosounder. The
area of possible influence of the multibeam 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 SIO’s
operations, the individual pulses would
be very short, and a given mammal
would not receive many of the
downward-directed pulses as the vessel
passes by. Possible effects of a multibeam echosounder on marine mammals
are described below.
Stranding—In 2013, an International
Scientific Review Panel investigated a
2008 mass stranding of approximately
100 melon-headed whales in a
Madagascar lagoon system (Southall et
al., 2013) associated with the use of a
high-frequency mapping system. The
report indicated that the use of a 12 kHz
multi-beam echosounder was the most
plausible and likely initial behavioral
trigger of the mass stranding event. This
was the first time that a relatively highfrequency mapping sonar system has
been associated with a stranding event.
However, the report also notes that there
were several site- and situation-specific
secondary factors that may have
contributed to the avoidance responses
that lead to the eventual entrapment and
mortality of the whales within the Loza
Lagoon system (e.g., the survey vessel
transiting in a north-south direction on
the shelf break parallel to the shore may
have trapped the animals between the
sound source and the shore driving
them towards the Loza Lagoon). The
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report concluded that for odontocete
cetaceans that hear well in the 10 to 50
kHz range, where ambient noise is
typically quite low, high-power active
sonars operating in this range may be
more easily audible and have potential
effects over larger areas than lowfrequency systems that have more
typically been considered in terms of
anthropogenic noise impacts (Southall
et al., 2013). However, the risk may be
very low given the extensive use of
these systems worldwide on a daily
basis and the lack of direct evidence of
such responses previously (Southall et
al., 2013). It is noted that leading
scientific experts on multi-beam
echosounders have expressed concerns
about the independent scientific review
panel analyses and findings (Bernstein,
2013).
Masking—Marine mammal
communications would not be masked
appreciably by the multi-beam
echosounder 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 multi-beam echosounder
signals (12 kHz) generally do not
overlap with the predominant
frequencies in the calls (16 Hz to less
than 12 kHz), which would avoid any
significant masking (Richardson et al.,
1995).
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 (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
(656.2 ft) (Frankel, 2005). When a 38
kHz echosounder and a 150 kHz ADCP
were transmitting during studies in the
Eastern Tropical Pacific, 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 second
tonal signals at frequencies similar to
those that would be emitted by the
multi-beam echosounder used by SIO,
and to shorter broadband pulsed signals.
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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 a multi-beam echosounder.
Risch et al. (2012) found a reduction
in humpback whale song in the
Stellwagen Bank National Marine
Sanctuary during Ocean Acoustic
Waveguide Remote Sensing (OAWRS)
activities that were carried out
approximately 200 km (108 nmi) away.
The OAWRS used three frequencymodulated pulses centered at
frequencies of 415, 734, and 949 Hz
with received levels in the sanctuary of
88 to 110 dB re 1 mPa. Deng et al. (2014)
measured the spectral properties of
pulses transmitted by three 200 kHz
echosounders, and found that they
generated weaker sounds at frequencies
below the center frequency (90 to 130
kHz). These sounds are within the
hearing range of some marine mammals,
and the authors suggested that they
could be strong enough to elicit
behavioral responses within close
proximity to the sources, although they
would be well below potentially
harmful levels.
Hearing Impairment and Other
Physical Effects—Given several
stranding events that have been
associated with the operation of naval
sonar in specific circumstances, there is
concern that mid-frequency sonar
sounds can cause serious impacts to
marine mammals (see above). However,
the multi-beam echosounder proposed
for use by SIO is quite different than
sonar used for Navy operations. Pulse
duration of the multi-beam echosounder
is very short relative to the naval sonar.
Also, at any given location, an
individual marine mammal would be in
the beam of the multi-beam
echosounder for much less time, given
the generally downward orientation of
the beam and its narrow fore-aft
beamwidth; Navy sonar often uses nearhorizontally-directed sound and have
higher duty cycles. Those factors would
all reduce the sound energy received
from the multi-beam echosounder rather
drastically relative to that from naval
sonar. NMFS believes that the brief
exposure of marine mammals to one
pulse, or small numbers of signals, from
the multi-beam echosounder in this
particular case is not likely to result in
the harassment of marine mammals.
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Sub-Bottom Profiler
SIO would operate a sub-bottom
profiler (Knudsen 3260) from the source
vessel during the proposed study.
Sounds from the sub-bottom profiler are
very short pulses, occurring for 1 to 4
ms once ever second. Most of the energy
in the sound pulses emitted by the subbottom profiler is at frequencies 3.5
kHz, and the beam is directed
downward. The sub-bottom profiler that
may be used on the Revelle has a
maximum source level of 204 dB re 1
mPa. The sonar emits energy in a 27°
beam from the bottom of the ship.
Marine mammals that encounter the
Knudsen 3260 are unlikely to be
subjected to repeated pulses because of
the relatively narrow fore–aft width of
the beam and would receive only
limited amounts of pulse energy
because of the short pulses. Animals
close to the ship (where the beam is
narrowest) are especially unlikely to be
ensonified for more than one 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 a sub-bottom profiler emits a
pulse is small—even for a sub-bottom
profiler more powerful than that that
may be on the Revelle. The animal
would have to pass the transducer at
close range and be swimming at speeds
similar to the vessel in order to receive
the multiple pulses that might result in
sufficient exposure to cause TTS.
Navy sonars that have been linked to
avoidance reactions and stranding of
cetaceans: (1) Generally have longer
pulse duration than the Knudsen 3260;
and (2) are often directed close to
horizontally versus more downward for
the sub-bottom profiler. The area of
possible influence of the single-beam
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 SIO’s operations, the
individual pulses would be very short,
and a given mammal would not receive
many of the downward-directed pulses
as the vessel passes by. Possible effects
of a sub-bottom profiler on marine
mammals are described below.
Masking—Marine mammal
communications would not be masked
appreciably by the sub-bottom profiler
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 baleen whales, the sub-bottom
profiler signals do not overlap with the
predominant frequencies in the calls (16
Hz to less than 12 kHz), which would
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avoid any significant masking
(Richardson et al., 1995).
Behavioral Responses—Marine
mammal behavioral reactions to other
pulsed sound sources are discussed
above, and responses to the sub-bottom
profiler are likely to be similar to those
for other pulsed sources if received at
the same levels. However, the pulsed
signals from the sub-bottom profiler are
considerably weaker than those from the
multi-beam 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
sub-bottom 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 subbottom profiler is usually operated
simultaneously with other higher-power
acoustic sources, including airguns.
Many marine mammals will move away
in response to the approaching higherpower 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
sub-bottom profiler.
Heat-Flow Probe Deployment
During heat-flow measurements using
a probe, the probe is a passive
instrument and no noise is created by
the mechanical action of the devices on
the seafloor is not expected to be
perceived by nearby fish and other
marine organisms. Heat-flow
measurement activities would be highly
localized and short-term in duration and
would not be expected to significantly
interfere with marine mammal behavior.
The potential direct effects include
temporary localized disturbance or
displacement from associated physical
movement/actions of the operations.
Additionally, the potential indirect
effects may consist of very localized and
transitory/short-term disturbance of
bottom habitat and associated prey in
shallow-water areas as a result of heatflow probe measurements. NMFS
believes that the since the heat-flow
probe is a passive instrument and has
no mechanical action, it would not
likely result in the harassment of marine
mammals.
A maximum total of 200 heat-flow
measurements would be obtained using
these devices and ranging from 1 to 2
hours per measurement (for a total of
approximately 320 hours of operations)
and it is estimated that the pinger would
operate continuously during each heatflow probe deployment. The vessel
would be stationary during heat-flow
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probe deployment and repositioned to
repeat the process, so the likelihood of
a collision or entanglement with a
marine mammal is very low. For the
heat-flow measurements, the lance is 4.5
m and would disturb an area
approximately 8 cm x 20 cm (3.1 in x
7.9 in). Assuming approximately 200
heat-flow measurements, the cumulative
area of seafloor that could be disturbed
during the proposed study would be
approximately 32,000 cm2 (4,960 in2).
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 in 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 (especially low frequency
specialists) 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
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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’ reaction
varied when exposed to vessel noise
and traffic. In some cases, beluga whales
exhibited rapid swimming from icebreaking vessels up to 80 km (43.2 nmi)
away and showed changes in surfacing,
breathing, diving, and group
composition in the Canadian high
Arctic where vessel traffic is rare (Finley
et al., 1990). In other cases, beluga
whales were more tolerant of vessels,
but responded differentially to certain
vessels and operating characteristics by
reducing their calling rates (especially
older animals) in the St. Lawrence River
where vessel traffic is common (Blane
and Jaakson, 1994). In Bristol Bay,
Alaska, beluga whales continued to feed
when surrounded by fishing vessels and
resisted dispersal even when
purposefully harassed (Fish and Vania,
1971).
In reviewing more than 25 years of
whale observation data, Watkins (1986)
concluded that whale reactions to vessel
traffic were ‘‘modified by their previous
experience and current activity:
Habituation often occurred rapidly,
attention to other stimuli or
preoccupation with other activities
sometimes overcame their interest or
wariness of stimuli.’’ Watkins noticed
that over the years of exposure to ships
in the Cape Cod area, minke whales
changed from frequent positive interest
(e.g., approaching vessels) to generally
uninterested reactions; fin whales
changed from mostly negative (e.g.,
avoidance) to uninterested reactions; fin
whales changed from mostly negative
(e.g., avoidance) to uninterested
reactions; right whales apparently
continued the same variety of responses
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(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 whalewatching 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
Revelle would be audible to marine
mammals over a large distance, it is
unlikely that marine mammals would
respond behaviorally (in a manner that
NMFS would consider harassment
under the MMPA) to low-level distant
shipping noise as the animals in the
area are likely to be habituated to such
noises (Nowacek et al., 2004). In light of
these facts, NMFS does not expect the
Revelle’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 dolphins) 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;
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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
13 kts (24.1 km/hr, 14.9 mph).
SIO’s proposed operation of one
source vessel for the proposed lowenergy seismic survey is relatively small
in scale (i.e., a one vessel operation)
compared to the number of other ships
(e.g., fishing, tourist, and other vessels)
transiting at higher speeds in the same
areas on an annual basis. The
probability of vessel and marine
mammal interactions occurring during
the proposed low-energy seismic survey
is unlikely due to the Revelle’s slow
operational speed, which is typically 5
kts. Outside of seismic operations, the
Revelle’s cruising speed would be
approximately 10.1 to 14.5 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 Revelle has a
number of other advantages for avoiding
ship strikes as compared to most
commercial merchant vessels, including
the following: The Revelle’s bridge and
other observing stations offer good
visibility to visually monitor for marine
mammal presence; PSOs posted during
operations scan the ocean for marine
mammals and must report visual alerts
of marine mammal presence to crew;
and the PSOs 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 low-energy seismic survey
would require towing approximately
one 600 m cable streamers. While
towing this size of an array carries some
level of risk of entanglement for marine
mammals due to the operational nature
of the activity, entanglement is unlikely.
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. In May
2011, there was one recorded
entrapment of an olive ridley sea turtle
(Lepidochelys olivacea) in the R/V
Marcus G. Langseth’s barovanes after
the conclusion of a seismic survey off
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Costa Rica. There have been cases of
baleen whales, mostly gray whales
(Heyning, 1990), becoming entangled in
fishing lines. The probability for
entanglement of marine mammals is
considered very low because of the
vessel speed and the monitoring efforts
onboard the survey vessel. Furthermore,
there has been no history of marine
mammal entanglement with seismic
equipment used by the U.S. academic
research fleet.
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 impact on affected marine
mammal species and stocks.
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Anticipated Effects on Marine Mammal
Habitat
The proposed low-energy seismic
survey is not anticipated to have any
permanent impact on habitats used by
the marine mammals in the proposed
study area, including the food sources
they use (i.e. fish and invertebrates).
Additionally, no physical damage to any
habitat is anticipated as a result of
conducting airgun operations during the
proposed low-energy seismic survey.
While it is anticipated that the specified
activity may result in marine mammals
avoiding certain areas due to brief,
temporary ensonification, this impact to
habitat is temporary 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 in
any particular area of the approximately
1,154 km 2 proposed study area,
previously discussed in this notice.
The next section discusses the
potential impacts of anthropogenic
sound sources on common marine
mammal prey in the proposed study
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 and invertebrate populations is
limited. There are three types of
potential effects of exposure to seismic
surveys: (1) Pathological, (2)
physiological, and (3) behavioral.
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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. This makes drawing
conclusions about impacts on fish
problematic because, ultimately, the
most important issues concern effects
on marine fish populations, their
viability, and their availability to
fisheries.
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
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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. There are only two
known papers with proper experimental
methods, controls, and careful
pathological investigation implicating
sounds produced by actual seismic
survey airguns in causing adverse
anatomical effects. One such study
indicated anatomical damage, and the
second indicated TTS in fish hearing.
The anatomical case is McCauley et al.
(2003), who found that exposure to
airgun sound caused observable
anatomical damage to the auditory
maculae of pink snapper (Pagrus
auratus). This damage in the ears had
not been repaired in fish sacrificed and
examined almost two months after
exposure. On the other hand, Popper et
al. (2005) documented only TTS (as
determined by auditory brainstem
response) in two of three fish species
from the Mackenzie River Delta. This
study found that broad whitefish
(Coregonus nasus) exposed to five
airgun shots were not significantly
different from those of controls. During
both studies, the repetitive exposure to
sound was greater than would have
occurred during a typical seismic
survey. However, the substantial lowfrequency energy produced by the
airguns (less than 400 Hz in the study
by McCauley et al. [2003] and less than
approximately 200 Hz in Popper et al.
[2005]) likely did not propagate to the
fish because the water in the study areas
was very shallow (approximately nine
m in the former case and less than two
m in the latter). Water depth sets a
lower limit on the lowest sound
frequency that would propagate (the
‘‘cutoff frequency’’) at about one-quarter
wavelength (Urick, 1983; Rogers and
Cox, 1988).
Wardle et al. (2001) suggested that in
water, acute injury and death of
organisms exposed to seismic energy
depends primarily on two features of
the sound source: (1) The received peak
pressure, and (2) the time required for
the pressure to rise and decay.
Generally, as received pressure
increases, the period for the pressure to
rise and decay decreases, and the
chance of acute pathological effects
increases. According to Buchanan et al.
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(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). The airgun was suspended 3.5 m
(11.5 ft) above a school of threadfin shad
in Lake Meade and was 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
death of any of the fish carcasses
observed. They also concluded that 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
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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 former Minerals Management
Service (MMS, 2005) assessed the
effects of a proposed seismic survey in
Cook Inlet. The seismic survey proposed
using three vessels, each towing two
four-airgun arrays ranging from 24,580.6
to 40,967.7 cm3 (1,500 to 2,500 in3).
MMS noted that the impact to fish
populations in the survey area and
adjacent waters would likely be very
low and temporary. MMS 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.
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Anticipated Effects on Invertebrates
The existing body of information on
the impacts of seismic survey sound on
marine invertebrates is very limited.
However, there is some unpublished
and very limited evidence of the
potential for adverse effects on
invertebrates, thereby justifying further
discussion and analysis of this issue.
The three types of potential effects of
exposure to seismic surveys on marine
invertebrates are pathological,
physiological, and behavioral. Based on
the physical structure of their sensory
organs, marine invertebrates appear to
be specialized to respond to particle
displacement components of an
impinging sound field and not to the
pressure component (Popper et al.,
2001).
The only information available on the
impacts of seismic surveys on marine
invertebrates involves studies of
individuals; there have been no studies
at the population scale. Thus, available
information provides limited insight on
possible real-world effects at the
regional or ocean scale. The most
important aspect of potential impacts
concerns how exposure to seismic
survey sound ultimately affects
invertebrate populations and their
viability, including availability to
fisheries.
Literature reviews of the effects of
seismic and other underwater sound on
invertebrates were provided by
Moriyasu et al. (2004) and Payne et al.
(2008). The following sections provide a
synopsis of available information on the
effects of exposure to seismic survey
sound on species of decapod
crustaceans and cephalopods, the two
taxonomic groups of invertebrates on
which most such studies have been
conducted. The available information is
from studies with variable degrees of
scientific soundness and from anecdotal
information. A more detailed review of
the literature on the effects of seismic
survey sound on invertebrates is
provided in Appendix D of NSF/USGS’s
PEIS (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
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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
species of cephalopods (Loligo vulgaris,
Sepia officinalis, Octopus vulgaris, and
Ilex coindetii), primarily cuttlefish, to
two hours of continuous 50 to 400 Hz
sinusoidal wave sweeps at 157+/–5 dB
re 1 mPa while captive in relatively
small tanks. They reported
morphological and ultrastructural
evidence of massive acoustic trauma
(i.e., permanent and substantial
alterations [lesions] of statocyst sensory
hair cells) to the exposed animals that
increased in severity with time,
suggesting that cephalopods are
particularly sensitive to low frequency
sound. The received SPL was reported
as 157+/–5 dB re 1 mPa, with peak levels
at 175 dB re 1 mPa. As in the McCauley
et al. (2003) paper on sensory hair cell
damage in pink snapper as a result of
exposure to seismic sound, the
cephalopods were subjected to higher
sound levels than they would be under
natural conditions, and they were
unable to swim away from the sound
source.
Physiological Effects—Physiological
effects refer mainly to biochemical
responses by marine invertebrates to
acoustic stress. Such stress potentially
could affect invertebrate populations by
increasing mortality or reducing
reproductive success. Primary and
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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, that 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). More
information on the potential effects of
airguns on fish and invertebrates are
reviewed in section 3.2.4.3, section
3.3.4.3, and Appendix D of the NSF/
USGS PEIS (2011).
Proposed Mitigation
In order to issue an Incidental Take
Authorization (ITA) under section
101(a)(5)(D) of the MMPA, NMFS must
set forth the permissible methods of
taking pursuant to such activity, and
other means of effecting the least
practicable 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
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for taking for certain subsistence uses
(where relevant).
SIO reviewed the following source
documents and incorporated a suite of
appropriate mitigation measures into
the project description.
(1) Protocols used during previous
NSF and USGS-funded seismic research
cruises as approved by NMFS and
detailed in the ‘‘Final Programmatic
Environmental Impact Statement/
Overseas Environmental Impact
Statement for Marine Seismic Research
Funded by the National Science
Foundation or Conducted by the U.S.
Geological Survey;’’
(2) Previous IHA applications and
IHAs approved and authorized by
NMFS; and
(3) Recommended best practices in
Richardson et al. (1995), Pierson et al.
(1998), and Weir and Dolman, (2007).
To reduce the potential for
disturbance from acoustic stimuli
associated with the activities, SIO
proposed to implement the following
mitigation measures for marine
mammals:
(1) Proposed exclusion zones around
the sound source;
(2) Speed and course alterations;
(3) Shut-down procedures; and
(4) Ramp-up procedures.
Proposed Exclusion Zones—During
pre-planning of the cruise, the smallest
airgun array was identified that could be
used and still meet the geophysical
scientific objectives. SIO use radii to
designate exclusion and buffer zones
and to estimate take for marine
mammals. Table 2 (presented earlier in
this document) shows the distances at
which one would expect to receive three
sound levels (160, 180, and 190 dB)
from the two GI airgun array. The 180
and 190 dB level shut-down criteria are
applicable to cetaceans and pinnipeds,
respectively, as specified by NMFS
(2000) and would be used to establish
the exclusion and buffer zones.
Received sound levels have been
modeled by L–DEO for a number of
airgun configurations, including two 45
in 3 Nucleus G airguns, in relation to
distance and direction from the airguns
(see Figure 2 of the IHA application). In
addition, propagation measurements of
pulses from two GI airguns have been
reported for shallow water
(approximately 30 m [98.4 ft] depth) in
the Gulf of Mexico (Tolstoy et al., 2004).
However, measurements were not made
for the two GI airguns in deep water.
The model does not allow for bottom
interactions, and is most directly
applicable to deep water. Based on the
modeling, estimates of the maximum
distances from the GI airguns where
sound levels are predicted to be 190,
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180, and 160 dB re 1 mPa (rms) in
intermediate and deep water were
determined (see Table 2 above).
Empirical data concerning the 190,
180, and 160 dB (rms) distances were
acquired for various airgun arrays based
on measurements during the acoustic
verification studies conducted by
L–DEO in the northern Gulf of Mexico
in 2003 (Tolstoy et al., 2004) and 2007
to 2008 (Tolstoy et al., 2009). Results of
the 18 and 36 airgun arrays are not
relevant for the two GI airguns to be
used in the proposed low-energy
seismic survey because the airgun arrays
are not the same size or volume. The
empirical data for the 6, 10, 12, and 20
airgun arrays indicate that, for deep
water, the L–DEO model tends to
overestimate the received sound levels
at a given distance (Tolstoy et al., 2004).
Measurements were not made for the
two GI airgun array in deep water;
however, SIO proposes to use the safety
radii predicted by L–DEO’s model for
the proposed GI airgun operations in
intermediate and deep water, although
they are likely conservative given the
empirical results for the other arrays.
Based on the modeling data, the
outputs from the pair of 45 in 3 GI
airguns proposed to be used during the
low-energy seismic survey are
considered a low-energy acoustic source
in the NSF/USGS PEIS (2011) for
marine seismic research. A low-energy
seismic source was defined in the NSF/
USGS PEIS as an acoustic source whose
received level is less than or equal to180
dB at 100 m (including any single or any
two GI airguns and a single pair of
clustered airguns with individual
volumes of less than or equal to 250
in 3). The NSF/USGS PEIS also
established for these low-energy sources
a standard exclusion zone of 100 m for
all low-energy sources in water depths
greater than 100 m. This standard 100
m exclusion zone would be used during
the proposed low-energy seismic survey
using the pair of 45 in 3 GI airguns. The
180 and 190 dB (rms) radii are the
current Level A harassment shut-down
criteria applicable to cetaceans and
pinnipeds, respectively; these levels
were used to establish exclusion zones.
Therefore, the assumed 180 and 190 dB
radii are 100 m for intermediate and
deep water. If the PSO detects a marine
mammal within or about to enter the
appropriate exclusion zone, the airguns
would be shut down immediately.
Speed and Course Alterations—If a
marine mammal is detected outside the
exclusion zone and, based on its
position and direction of travel (relative
motion), is likely to enter the exclusion
zone, changes of the vessel’s speed and/
or direct course would be considered if
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this does not compromise operational
safety or damage the deployed
equipment. This would be done if
operationally practicable while
minimizing the effect on the planned
science objectives. For marine seismic
surveys towing large streamer arrays,
course alterations are not typically
implemented due to the vessel’s limited
maneuverability. However, the Revelle
would be towing a relatively short
hydrophone streamer, so its
maneuverability during operations with
the hydrophone streamer would not be
limited as vessels towing long
streamers, thus increasing the potential
to implement course alterations, if
necessary. After any such speed and/or
course alteration is begun, the marine
mammal activities and movements
relative to the seismic vessel would be
closely monitored to ensure that the
marine mammal does not approach
within the applicable exclusion zone. If
the marine mammal appears likely to
enter the exclusion zone, further
mitigation actions would be taken,
including further speed and/or course
alterations, and/or shut-down of the
airgun(s). Typically, during airgun
operations, the source vessel is unable
to change speed or course, and one or
more alternative mitigation measures
would need to be implemented.
Shut-Down Procedures—If a marine
mammal is detected outside the
exclusion zone for the airgun(s) but is
likely to enter the exclusion zone, and
the vessel’s speed and/or course cannot
be changed to avoid having the animal
enter the exclusion zone, SIO would
shut-down the operating airgun(s)
before the animal is within the
exclusion zone. Likewise, if a marine
mammal is already within the exclusion
zone when first detected, the airguns
would be shut-down immediately.
Following a shut-down, SIO would
not resume airgun activity until the
marine mammal has cleared the
exclusion zone, or until the PSO is
confident that the animal has left the
vicinity of the vessel. SIO would
consider the animal to have cleared the
exclusion zone if:
• A PSO has visually observed the
animal leave the exclusion zone, or
• A PSO has not sighted the animal
within the exclusion zone for 15
minutes for species with shorter dive
durations (i.e., small odontocetes and
pinnipeds), or 30 minutes for species
with longer dive durations (i.e.,
mysticetes and large odontocetes,
including sperm, dwarf and pygmy
sperm, killer, and beaked whales).
Although power-down procedures are
often standard operating practice for
seismic surveys, they are not proposed
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to be used during this planned lowenergy seismic survey because powering
down from two airguns to one airgun
would make only a small difference in
the exclusion zone(s) that probably
would not be enough to allow continued
one-airgun operations if a marine
mammal came within the exclusion
zone for two airguns.
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, avoiding any potential
injury or impairment of their hearing
abilities. SIO would follow a ramp-up
procedure when the airgun array begins
operating after a specified period
without airgun operations or when a
shut-down has exceeded that period.
SIO proposes that, for the present
cruise, this period would be
approximately 15 minutes. SIO, L–DEO,
USGS, NSF, and ASC have used similar
periods (approximately 15 minutes)
during previous low-energy seismic
surveys.
Ramp-up would begin with a single
GI airgun (45 in 3). The second GI airgun
(45 in 3) would be added after 5
minutes. During ramp-up, the PSOs
would monitor the exclusion zone, and
if marine mammals are sighted, a shutdown would be implemented as though
both GI airguns 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, SIO would not
commence the ramp-up. Given these
provisions, it is likely that the airgun
array would not be ramped-up from a
complete shut-down during low light
conditions, at night, or in thick fog, (i.e.,
poor visibility conditions) because the
outer part of the exclusion zone for that
array would not be visible during those
conditions. If one airgun has been
operating, ramp-up to full power would
be permissible during low light, 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 if
they choose. SIO would not initiate a
ramp-up of the airguns if a marine
mammal is sighted within or near the
applicable exclusion zones during day
or night. NMFS refers the reader to
Figure 2, which presents a flowchart
representing the ramp-up and shutdown protocols described in this notice.
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Proposed Mitigation Conclusions
NMFS has carefully evaluated the
applicant’s proposed mitigation
measures and has considered a range of
other measures in the context of
ensuring that NMFS prescribes the
means of effecting the least practicable
impact on the affected marine mammal
species and stocks and their habitat.
NMFS’s evaluation of potential
measures included consideration of the
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following factors in relation to one
another:
(1) The manner in which, and the
degree to which, the successful
implementation of the measure is
expected to minimize adverse impacts
to marine mammals;
(2) The proven or likely efficacy of the
specific measure to minimize adverse
impacts as planned; and
(3) The practicability of the measure
for applicant implementation.
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Any mitigation measure(s) prescribed
by NMFS should be able to accomplish,
have a reasonable likelihood of
accomplishing (based on current
science), or contribute to the
accomplishment of one or more of the
general goals listed below:
(1) Avoidance of minimization of
injury or death of marine mammals
wherever possible (goals 2, 3, and 4 may
contribute to this goal).
(2) A reduction in the numbers of
marine mammals (total number or
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number at biologically important time
or location) exposed to received levels
of airguns, or other activities expected
to result in the take of marine mammals
(this goal may contribute to 1, above, or
to reducing harassment takes only).
(3) A reduction in the number of time
(total number or number at biologically
important time or location) individuals
would be exposed to received levels of
airguns, or other activities expected to
result in the take of marine mammals
(this goal may contribute to 1, above, or
to reducing harassment takes only).
(4) A reduction in the intensity of
exposures (either total number or
number at biologically important time
or location) to received levels of airguns,
or other activities, or other activities
expected to result in the take of marine
mammals (this goal may contribute to a,
above, or to reducing the severity of
harassment takes only).
(5) Avoidance or minimization of
adverse effects to marine mammal
habitat, paying special attention to the
food base, activities that block or limit
passage to or from biologically
important areas, permanent destruction
of habitat, or temporary destruction/
disturbance of habitat during a
biologically important time.
(6) For monitoring directly related to
mitigation—an increase in the
probability of detecting marine
mammals, thus allowing for more
effective implementation of the
mitigation.
Based on NMFS’s evaluation of the
applicant’s proposed measures, as well
as other measures considered by NMFS
or recommended by the public, NMFS
has preliminarily determined that the
proposed mitigation measures provide
the means of effecting the least
practicable impact on marine mammal
species or stocks and their habitat,
paying particular attention to rookeries,
mating grounds, and areas of similar
significance.
Proposed Monitoring and Reporting
In order to issue an ITA for an
activity, section 101(a)(5)(D) of the
MMPA states that NMFS must set forth
‘‘requirements pertaining to the
monitoring and reporting of such
taking.’’ The MMPA implementing
regulations at 50 CFR 216.104(a)(13)
indicate that requests for IHAs must
include the suggested means of
accomplishing the necessary monitoring
and reporting that would result in
increased knowledge of the species and
of the level of taking or impacts on
populations of marine mammals that are
expected to be present in the proposed
action area. SIO submitted a marine
mammal monitoring plan as part of the
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IHA application. It can be found in
Section 13 of the IHA application. The
plan may be modified or supplemented
based on comments or new information
received from the public during the
public comment period.
Monitoring measures prescribed by
NMFS should accomplish one or more
of the following general goals:
(1) An increase in the probability of
detecting marine mammals, both within
the mitigation zone (thus allowing for
more effective implementation of the
mitigation) and in general to generate
more data to contribute to the analyses
mentioned below;
(2) An increase in our understanding
of how many marine mammals are
likely to be exposed to levels of sound
(airguns) that we associate with specific
adverse effects, such as behavioral
harassment, TTS, or PTS;
(3) An increase in our understanding
of how marine mammals respond to
stimuli expected to result in take and
how anticipated adverse effects on
individuals (in different ways and to
varying degrees) may impact the
population, species, or stock
(specifically through effects on annual
rates of recruitment or survival) through
any of the following methods:
• Behavioral observations in the
presence of stimuli compared to
observations in the absence of stimuli
(need to be able to accurately predict
received level, distance from source,
and other pertinent information);
• Physiological measurements in the
presence of stimuli compared to
observations in the absence of stimuli
(need to be able to accurately predict
received level, distance from source,
and other pertinent information); and
• Distribution and/or abundance
comparisons in times or areas with
concentrated stimuli versus times or
areas without stimuli;
(4) An increased knowledge of the
affected species; and
(5) An increase in our understanding
of the effectiveness of certain mitigation
and monitoring measures.
Proposed Monitoring
SIO proposes to sponsor marine
mammal monitoring during the
proposed project, in order to implement
the proposed mitigation measures that
require real-time monitoring and to
satisfy the anticipated monitoring
requirements of the IHA. SIO’s proposed
‘‘Monitoring Plan’’ is described below
this section. The monitoring work
described here has been planned as a
self-contained project independent of
any other related monitoring projects
that may be occurring simultaneously in
the same regions. SIO is prepared to
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discuss coordination of their monitoring
program with any related work that
might be done by other groups insofar
as this is practical and desirable.
Vessel-Based Visual Monitoring
PSOs would be based aboard the
seismic source vessel and would watch
for marine mammals near the vessel
during daytime airgun operations and
during any ramp-ups of the airguns at
night. PSOs would also watch for
marine mammals near the seismic
vessel for at least 30 minutes prior to the
start of airgun operations and after an
extended shut-down (i.e., greater than
approximately 15 minutes for this
proposed low-energy seismic survey).
When feasible, PSOs would conduct
observations during daytime periods
when the seismic system is not
operating (such as during transits) for
comparison of sighting rates and
behavior with and without airgun
operations and between acquisition
periods. Based on PSO observations, the
airguns would be shut-down when
marine mammals are observed within or
about to enter a designated exclusion
zone.
During airgun operations in the
Southwest Pacific Ocean, East of New
Zealand, at least three PSOs would be
based aboard the Revelle. At least one
PSO would stand watch at all times
while the Revelle is operating airguns
during the proposed low-energy seismic
survey; this procedure would also be
followed when the vessel is in transit.
SIO would appoint the PSOs with
NMFS’s concurrence. The lead PSO
would be experienced with marine
mammal species in the Pacific Ocean
and/or off the east coast of New
Zealand, the second and third PSOs
would receive additional specialized
training from the lead PSO to ensure
that they can identify marine mammal
species commonly found in the
Southwest Pacific Ocean. Observations
would take place during ongoing
daytime operations and ramp-ups of the
airguns. During the majority of seismic
operations, at least one PSO would be
on duty from observation platforms (i.e.,
the best available vantage point on the
source vessel) to monitor marine
mammals near the seismic vessel.
PSO(s) would be on duty in shifts no
longer than 4 hours in duration. Other
crew would also be instructed to assist
in detecting marine mammals and
implementing mitigation requirements
(if practical). Before the start of the lowenergy seismic survey, the crew would
be given additional instruction on how
to do so.
The Revelle is a suitable platform for
marine mammal observations and
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would serve as the platform from which
PSOs would watch for marine mammals
before and during airgun operations.
The Revelle has been used for marine
mammal observations during the
routine California Cooperative Oceanic
Fisheries Investigations (CalCOFI). Two
locations are likely as observation
stations onboard the Revelle. Observing
stations are located at the 02 level, with
PSO eye level at approximately 10.4 m
(34 ft) above the waterline and the PSO
would have a good view around the
entire vessel. At a forward-centered
position on the 02 deck, the view is
approximately 240° around the vessel;
and one atop the aft hangar, with an aftcentered view includes the 100 m radius
around the GI airguns. The PSO eye
level on the bridge is approximately 15
m (49.2 ft) above sea level. PSOs would
work on the enclosed bridge and
adjoining aft steering station during any
inclement weather.
Standard equipment for PSOs would
be reticle binoculars and optical range
finders. Night-vision equipment would
be available at night and low-light
conditions during the cruise. The PSOs
would be in communication with ship’s
officers on the bridge and scientists in
the vessel’s operations laboratory, so
they can advise promptly of the need for
avoidance maneuvers or seismic source
shut-down. During daylight, the PSO(s)
would scan the area around the vessel
systematically with reticle binoculars
(e.g., 7 x 50 Fujinon FMTRC–SX), Bigeye binoculars (e.g., 25 x 150 Fujinon
MT), optical range-finders (to assist with
distance estimation), and the naked eye.
These binoculars would have a built-in
daylight compass. Estimating distances
is done primarily with the reticles in the
binoculars. The optical range-finders are
useful in training PSOs to estimate
distances visually, but are generally not
useful in measuring distances to
animals directly. At night, night-vision
equipment would be available. The
PSO(s) would be in direct (radio)
wireless communication with ship’s
officers on the bridge and scientists in
the vessel’s operations laboratory during
seismic operations, so they can advise
the vessel operator, science support
personnel, and the science party
promptly of the need for avoidance
maneuvers or a shut-down of the
seismic source.
When a marine mammal is detected
within or about to enter the designated
exclusion zone, the airguns would
immediately be shut-down, unless the
vessel’s speed and/or course can be
changed to avoid having the animal
enter the exclusion zone. The PSO(s)
would continue to maintain watch to
determine when the animal is outside
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the exclusion zone by visual
confirmation. Airgun operations would
not resume until the animal is
confirmed to have left the exclusion
zone, or is 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, dwarf
and pygmy sperm, killer, and beaked
whales).
PSO Data and Documentation
PSOs 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.
Data would be used to estimate numbers
of animals potentially ‘‘taken’’ by
harassment. They would also provide
information needed to order a shutdown of the airguns when a marine
mammal is within or near the exclusion
zone. Observations would also be made
during daylight periods when the
Revelle is underway without seismic
airgun operations (i.e., transits to, from,
and through the study area) to collect
baseline biological data.
When a sighting is made, the
following information about the sighting
would be recorded:
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
seismic source or vessel (e.g., none,
avoidance, approach, paralleling, etc.),
and behavioral pace.
2. Time, location, heading, speed,
activity of the vessel (including number
of airguns operating and whether in
state of ramp-up or shut-down), sea
state, wind force, visibility, cloud cover,
and sun glare.
The data listed under (2) would also
be recorded at the start and end of each
observation watch, and during a watch
whenever there is a change in one or
more of the variables.
All observations, as well as
information regarding ramp-ups or shutdowns, would be recorded in a
standardized format. Data would be
entered into an electronic database. The
data accuracy would be verified by
computerized data validity checks as
the data are entered and by subsequent
manual checking of the database by the
PSOs at sea. These procedures would
allow initial summaries of data to be
prepared during and shortly after the
field program, and would facilitate
transfer of the data to statistical,
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graphical, and other programs for
further processing and archiving.
Results from the vessel-based
observations would provide the
following information:
1. The basis for real-time mitigation
(airgun shut-down).
2. Information needed to estimate the
number of marine mammals potentially
taken by harassment, which must be
reported to NMFS.
3. Data on the occurrence,
distribution, and activities of marine
mammals in the area where the seismic
study is conducted.
4. Information to compare the
distance and distribution of marine
mammals relative to the source vessel at
times with and without airgun
operations.
5. Data on the behavior and
movement patterns of marine mammals
seen at times with and without airgun
operations.
Proposed Reporting
SIO would submit a comprehensive
report to NMFS and NSF within 90 days
after the end of the cruise. The report
would describe the operations that were
conducted and sightings of marine
mammals near the operations. The
report submitted to NMFS and NSF
would provide full documentation of
methods, results, and interpretation
pertaining to all monitoring. The 90-day
report would summarize the dates and
locations of airgun operations and all
marine mammal sightings (i.e., dates,
times, locations, activities, and
associated seismic survey activities).
The report would include, at a
minimum:
• Summaries of monitoring effort—
total hours, total distances, and
distribution of marine mammals
through the study period accounting for
Beaufort sea state and other factors
affecting visibility and detectability of
marine mammals;
• Analyses of the effects of various
factors influencing detectability of
marine mammals including Beaufort sea
state, number of PSOs, and fog/glare;
• Species composition, occurrence,
and distribution of marine mammals
sightings including date, water depth,
numbers, age/size/gender, and group
sizes, and analyses of the effects of
airgun operations;
• Sighting rates of marine mammals
during periods with and without airgun
operations (and other variables that
could affect detectability);
• Initial sighting distances versus
airgun operations state;
• Closest point of approach versus
airgun operations state;
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• Observed behaviors and types of
movements versus airgun operations
activity state;
• Numbers of sightings/individuals
seen versus airgun operations state; and
• Distribution around the source
vessel versus airgun operations state.
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. NMFS would review the
draft report and provide any comments
it may have, and SIO would incorporate
NMFS’s comments and prepare a final
report. After the report is considered
final, it would be publicly available on
the NMFS Web site at: https://
www.nmfs.noaa.gov/pr/permits/
incidental/.
Reporting Prohibited Take—In the
unanticipated event that the specified
activity clearly causes the take of a
marine mammal in a manner prohibited
by this IHA, such as an injury (Level A
harassment), serious injury or mortality
(e.g., ship-strike, gear interaction, and/or
entanglement), SIO would immediately
cease the specified activities and
immediately report the incident to the
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS at 301–427–8401 and/or by email
to Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov. The report
must include the following information:
• Time, date, and location (latitude/
longitude) of the incident;
• Name and type of vessel involved;
• Vessel’s speed during and leading
up to the incident;
• Description of the incident;
• Status of all sound source use in the
24 hours preceding the incident;
• Water depth;
• Environmental conditions (e.g.,
wind speed and direction, Beaufort sea
state, cloud cover, and visibility);
• Description of all marine mammal
observations in the 24 hours preceding
the incident;
• Species identification or
description of the animal(s) involved;
• Fate of the animal(s); and
• Photographs or video footage of the
animal(s) (if equipment is available).
Activities shall not resume until
NMFS is able to review the
circumstances of the prohibited take.
NMFS shall work with SIO to determine
what is necessary to minimize the
likelihood of further prohibited take and
ensure MMPA compliance. SIO may not
resume their activities until notified by
NMFS via letter or email, or telephone.
Reporting an Injured or Dead Marine
Mammal With an Unknown Cause of
Death—In the event that SIO discover
an injured or dead marine mammal, and
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the lead PSO determines that the cause
of the injury or death is unknown and
the death is relatively recent (i.e., in less
than a moderate state of decomposition),
SIO shall immediately report the
incident to the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, at 301–
427–8401, and/or by email to
Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov. The report
must include the same information
identified in the paragraph above.
Activities may continue while NMFS
reviews the circumstances of the
incident. NMFS shall work with SIO to
determine whether modifications in the
activities are appropriate.
Reporting an Injured or Dead Marine
Mammal Not Related to the Activities—
In the event that SIO discovers an
injured or dead marine mammal, and
the lead PSO determines that the injury
or death is not associated with or related
to the activities authorized in the IHA
(e.g., previously wounded animal,
carcass with moderate or advanced
decomposition, or scavenger damage),
SIO shall report the incident to the
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS, at 301–427–8401, and/or by
email to Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov, within 24
hours of discovery. SIO shall provide
photographs or video footage (if
available) or other documentation of the
stranded animal sighting to NMFS.
Activities may continue while NMFS
reviews the circumstances of the
incident.
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].
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TABLE 4—NMFS’S CURRENT UNDERWATER ACOUSTIC EXPOSURE CRITERIA
Criterion
definition
Criterion
Threshold
Impulsive (non-explosive) sound
Level A
harassment
(injury).
Level B
harassment.
Level B
harassment.
Permanent
threshold
shift (PTS)
(Any level
above that
which is
known to
cause TTS).
Behavioral disruption (for
impulsive
noise).
Behavioral disruption (for
continuous
noise).
180 dB re 1
μPa-m (root
means
square [rms])
(cetaceans)
190 dB re 1
μPa-m (rms)
(pinnipeds)
160 dB re 1
μPa-m (rms)
120 dB re 1
μPa-m (rms)
Level B harassment is anticipated and
proposed to be authorized as a result of
the proposed low-energy seismic survey
in the Southwest Pacific Ocean, East of
New Zealand. Acoustic stimuli (i.e.,
increased underwater sound) generated
during the operation of the seismic
airgun array are expected to result in the
behavioral disturbance of some marine
mammals. NMFS’s current underwater
exposure criteria for impulsive sound
are detailed in Table 4 (above). There is
no evidence that the planned activities
for which SIO seek the IHA could result
in injury, serious injury, or mortality.
The required mitigation and monitoring
measures would minimize any potential
risk for injury, serious injury, or
mortality.
The following sections describe SIO’s
methods to estimate take by incidental
harassment and present the applicant’s
estimates of the numbers of marine
mammals that could be affected. The
estimates are based on a consideration
of the number of marine mammals that
could be harassed during the
approximately 135 hours and 1,250 km
of seismic airgun operations with the
two GI airgun array to be used.
There are no known systematic
aircraft- or ship-based surveys
conducted for marine mammals stock
assessments and very limited
population information available for
marine mammals in offshore waters of
the Southwest Pacific Ocean off the east
coast of New Zealand. For most
cetacean species, SIO and NMFS used
densities from extensive NMFS
Southwest Fisheries Science Center
(SWFSC) cruises (Ferguson and Barlow,
2001, 2003; Barlow, 2003, 2010; Forney,
2007) in one province of Longhurst’s
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(2006) pelagic biogeography, the
California Current Province (CALC).
That province is similar to the South
Subtropical Convergence Province
(SSTC) in which the proposed lowenergy seismic survey is located, in that
productivity is high and large pelagic
fish such as tuna occur. Specifically,
SIO and NMFS used the 1986 to 1996
data from blocks 35, 36, 47, 48, 59, and
60 of Ferguson and Barlow (2001, 2003),
the 2001 data from Barlow (2003) for the
Oregon, Washington, and California
strata, and the 2005 and 2008 data from
Forney (2007) and Barlow (2010),
respectively, for the two strata
combined. The densities used were
effort-weighted means for the 10
locations (blocks or States). The surveys
off California, Oregon, and Washington
were conducted up to approximately
556 km (300.2 nmi) offshore, and most
of those data were from offshore areas
that overlap with the above blocks
selected from Ferguson and Barlow
(2001, 2003).
For pinnipeds, SIO and NMFS used
the densities in Bonnell et al. (1992) of
northern fur seals (Callorhinus ursinus)
and northern elephant seals in offshore
areas of the western U.S. (the only
species regularly present in offshore
areas there) to estimate the numbers of
pinnipeds that might be present off New
Zealand.
The marine mammal species that
would be encountered during the
proposed low-energy seismic survey
would be different from those sighted
during surveys off the western U.S. and
in the Eastern Tropical Pacific Ocean.
However, the overall abundances of
species groups with generally similar
habitat requirements are expected to be
roughly similar. Thus, SIO and NMFS
used the data described above to
estimate the group densities of beaked
whales, delphinids, small whales, and
mysticetes in the proposed study area.
SIO and NMFS then estimated the
relative abundance of individual
southern species within the species
groups using various surveys and other
information from areas near the study
area, and general information on
species’ distributions such as latitudinal
ranges and group sizes. Group densities
from northern species were multiplied
by their estimated relative abundance
off New Zealand divided by the relative
abundance for all species in the species
group to derive estimates for the
southern species (see Table 3 of the IHA
application).
Densities for several cetacean species
are available for the Southern Ocean
(Butterworth et al., 1994), as follows: (1)
For humpback, sei, fin, blue, sperm,
killer, and pilot whales in Antarctic
Management areas I to VI south of 60°
South, based on the 1978/1979 to 1984
and 1985/1986 to 1990/1991 IWC/IDCR
circumpolar sighting survey cruises, and
(2) for humpback, sei, fin, blue, and
sperm whales extrapolated to latitudes
30 to 40° South, 40 to 50° South, 50 to
60° South based on Japanese scouting
vessel data from 1965/1966 to
1977/1978 and 1978/1979 to 1987/1988.
SIO and NMFS calculated densities
based on abundance and surface areas
given in Butterworth et al. (1994) and
used the weighted or mean density for
the Regions V and/or VI (whichever is
available) due to locations that represent
foraging areas or distributions for
animals that are likely to move past
New Zealand during northerly
migrations or breed in New Zealand
waters.
The densities used for purposes of
estimating potential take do not take
into account the patchy distributions of
marine mammals in an ecosystem, at
least on the moderate to fine scales over
which they are known to occur. Instead,
animals are considered evenly
distributed throughout the assessed
study area and seasonal movement
patterns are not taken into account, as
none are available. Although there is
some uncertainty about the
representativeness of the data and the
assumptions used in the calculations
below, the approach used here is
believed to be the best available
approach, using the best available
science.
TABLE 5—ESTIMATED DENSITIES AND POSSIBLE NUMBER OF MARINE MAMMAL SPECIES THAT MIGHT BE EXPOSED TO
GREATER THAN OR EQUAL TO 160 dB (AIRGUN OPERATIONS) DURING SIO’S PROPOSED LOW-ENERGY SEISMIC SURVEY (APPROXIMATELY 1,250 km OF TRACKLINES/APPROXIMATELY 1,154 km 2 ENSONIFIED AREA FOR AIRGUN OPERATIONS) IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND, MAY TO JUNE 2015
Density U.S.
West Coast/
Southern
Ocean/estimate used
(number of
animals/1,000
km2) 1
Species
Calculated
take from seismic airgun operations (i.e.,
estimated
number of individuals exposed to
sound levels
≥160 dB re 1
μPa) 2
Proposed take
authorization 3
Abundance 4
Approximate percentage of population estimate
(proposed take) 5
Population
trend 6
Mysticetes
mstockstill on DSK4VPTVN1PROD with NOTICES2
Southern right
whale.
0.98/NA/0.98
1.13
2
8,000
to
15,000—Worldwide.
12,000—Southern Hemisphere.
2,700—Sub-Antarctic New Zealand.
Pygmy right
whale.
Humpback whale
0.39/NA/0.39
0.45
2
0.98/0.25/0.25
0.29
2
0.59/NA/0.59
0.68
2
Antarctic minke
whale.
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Increasing at 7
to 8% per
year.
NA .................................................
0.03—Worldwide. 0.02—
Southern
Hemisphere.
0.07—SubAntarctic New
Zealand.
NA .....................
35,000
to
42,000—Southern
Hemisphere.
720,000 to 750,000—Southern
Hemisphere.
<0.01—Southern
Hemisphere.
<0.01—Southern
Hemisphere.
Increasing.
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TABLE 5—ESTIMATED DENSITIES AND POSSIBLE NUMBER OF MARINE MAMMAL SPECIES THAT MIGHT BE EXPOSED TO
GREATER THAN OR EQUAL TO 160 dB (AIRGUN OPERATIONS) DURING SIO’S PROPOSED LOW-ENERGY SEISMIC SURVEY (APPROXIMATELY 1,250 km OF TRACKLINES/APPROXIMATELY 1,154 km 2 ENSONIFIED AREA FOR AIRGUN OPERATIONS) IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND, MAY TO JUNE 2015—Continued
Density U.S.
West Coast/
Southern
Ocean/estimate used
(number of
animals/1,000
km2) 1
Species
Calculated
take from seismic airgun operations (i.e.,
estimated
number of individuals exposed to
sound levels
≥160 dB re 1
μPa) 2
Proposed take
authorization 3
Abundance 4
Approximate percentage of population estimate
(proposed take) 5
<0.01—Southern
Hemisphere.
NA.
<0.01—Worldwide. <0.01—
Northwestern
Pacific Ocean
<0.01.
80,000—Worldwide.
10,000— <0.01—WorldSouth of Antarctic Convergence.
wide. 0.02—
South of Antarctic Convergence.
140,000—Worldwide.
15,000— <0.01—WorldSouth of Antarctic Convergence.
wide. 0.01—
South of Antarctic Convergence.
8,000
to
9,000—Worldwide. 0.03—World2,300—True Southern Hemiwide. 0.09—
sphere. 1,500—Pygmy.
True Southern
Hemisphere.
0.13—Pygmy.
NA.
Minke whale (including dwarf
minke whale
sub-species).
Bryde’s whale ....
0.59/NA/0.59
0.68
2
720,000 to 750,000—Southern
Hemisphere.
0.20/NA/0.20
0.23
2
At least 30,000 to 40,000—Worldwide.
21,000—Northwestern
Pacific Ocean 48,109.
Sei whale ...........
0.59/0.08/0.08
0.09
2
Fin whale ...........
0.59/0.13/0.13
0.15
2
Blue whale .........
0.59/0.05/0.05
0.06
2
Population
trend 6
NA.
NA.
NA.
Odontocetes
1.62/1.16/1.16
1.34
10
Pygmy sperm
whale.
Cuvier’s beaked
whale.
Shepherd’s
beaked whale.
Southern
bottlenose
whale.
mstockstill on DSK4VPTVN1PROD with NOTICES2
Sperm whale .....
0.97/NA/0.97
1.12
0.69/NA/0.69
Andrew’s beaked
whale.
Blainville’s
beaked whale.
Gray’s beaked
whale.
Hector’s beaked
whale.
Spade-toothed
beaked whale.
Strap-toothed
beaked whale.
Killer whale ........
False killer whale
VerDate Sep<11>2014
NA.
5
360,000—Worldwide.
30,000— <0.01—WorldSouth of Antarctic Convergence.
wide. 0.03—
South of Antarctic Convergence.
NA ................................................. NA .....................
0.80
2
600,000 .........................................
<0.01 .................
NA
0.46/NA/0.46
0.53
3
600,000 .........................................
<0.01 .................
NA.
0.46/NA/0.46
0.53
2
50,000—South of Antarctic Convergence 600,000.
NA.
0.46/NA/0.46
0.53
2
600,000 .........................................
<0.01—South of
Antarctic Convergence
<0.01.
<0.01 .................
NA.
0.23/NA/0.23
0.27
2
600,000 .........................................
<0.01 .................
NA.
0.92/NA/0.92
1.06
2
600,000 .........................................
<0.01 .................
NA.
0.46/NA/0.46
0.53
2
600,000 .........................................
<0.01 .................
NA.
0.23/NA/0.23
0.27
2
600,000 .........................................
<0.01 .................
NA.
0.69/NA/0.69
0.80
3
600,000 .........................................
<0.01 .................
NA.
0.45/5.70/5.70
6.58
12
80,000—South of Antarctic Convergence.
NA.
0.27/NA/0.27
0.31
10
NA .................................................
0.02—South of
Antarctic Convergence.
NA .....................
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NA.
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TABLE 5—ESTIMATED DENSITIES AND POSSIBLE NUMBER OF MARINE MAMMAL SPECIES THAT MIGHT BE EXPOSED TO
GREATER THAN OR EQUAL TO 160 dB (AIRGUN OPERATIONS) DURING SIO’S PROPOSED LOW-ENERGY SEISMIC SURVEY (APPROXIMATELY 1,250 km OF TRACKLINES/APPROXIMATELY 1,154 km 2 ENSONIFIED AREA FOR AIRGUN OPERATIONS) IN THE SOUTHWEST PACIFIC OCEAN, EAST OF NEW ZEALAND, MAY TO JUNE 2015—Continued
Species
Density U.S.
West Coast/
Southern
Ocean/estimate used
(number of
animals/1,000
km2) 1
Calculated
take from seismic airgun operations (i.e.,
estimated
number of individuals exposed to
sound levels
≥160 dB re 1
μPa) 2
Proposed take
authorization 3
Long-finned pilot
whale.
0.27/6.41/6.41
7.40
20
200,000—South of Antarctic Convergence.
Short-finned pilot
whale.
Bottlenose dolphin.
Dusky dolphin ....
0.45/NA/0.45
0.52
20
At least 600,000—Worldwide .......
81.55/NA/
81.55
81.55/NA/
81.55
32.62/NA/
32.62
48.93/NA/
48.93
94.11
95
At least 614,000—Worldwide .......
94.11
95
12,000 to 20,000—New Zealand
37.64
38
7,400 .............................................
56.47
57
144,000 to 150,000—South of
Antarctic Convergence.
163.10/NA/
163.10
188.22
189
At least 3,500,000—Worldwide ....
48.93/NA/
48.93
56.46
57
NA .................................................
Hector’s dolphin
Hourglass dolphin.
Short-beaked
common dolphin.
Southern right
whale dolphin.
Approximate percentage of population estimate
(proposed take) 5
Abundance 4
Population
trend 6
0.01—South of
Antarctic Convergence.
<0.01—Worldwide.
0.02—Worldwide
NA.
0.79—New Zealand.
0.51 ...................
NA.
0.04—South of
Antarctic Convergence.
<0.01—Worldwide.
NA.
NA .....................
NA.
NA.
Declining.
NA.
NA.
Pinnipeds
Southern elephant seal.
5.11/NA/5.11
New Zealand fur
seal.
5.90
6
640,000 to 650,000—Worldwide.
470,000—South Georgia Island
607,000.
12.79/NA/
12.79
14.76
15
135,000—Worldwide. 50,000 to
100,000—New Zealand.
<0.01—WorldIncreasing, dewide or South
creasing, or
Georgia Island.
stable depending on breeding population.
0.01—WorldIncreasing.
wide. 0.03—
New Zealand.
mstockstill on DSK4VPTVN1PROD with NOTICES2
NA = Not available or not assessed.
1 Densities based on sightings from NMFS SWFSC, IWC, and Bonnell et al. (2012) data.
2 Calculated take is estimated density multiplied by the area ensonified to 160 dB (rms) around the proposed seismic tracklines, increased by
25% for contingency.
3 Adjusted to account for average group size.
4 See population estimates for marine mammal species in Table 3 (above).
5 Total proposed authorized takes expressed as percentages of the species or regional populations.
6 Jefferson et al. (2008).
Numbers of marine mammals that
might be present and potentially
disturbed are estimated based on the
available data about marine mammal
distribution and densities in the U.S.
west coast and Southern Ocean as a
proxy for the proposed study area off
the east coast of New Zealand. SIO
estimated the number of different
individuals that may be exposed to
airgun sounds with received levels
greater than or equal to 160 dB re 1 mPa
(rms) for seismic airgun operations 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
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occasion and the expected density of
marine mammals in the area (in the
absence of the low-energy seismic
survey). The number of possible
exposures can be estimated by
considering the total marine area that
would be within the 160 dB radius (the
diameter is 400 m multiplied by 2 for
deep water depths, the diameter is 600
m multiplied by 2 for intermediate
water depths) around the operating
airguns, including areas of overlap. The
spacing of tracklines is 500 m (1,640.4
ft) in the smaller grids and 1,250 m
(4,101.1 ft) in the larger grids. Overlap
was measured using GIS and was
minimal (area with overlap is equal to
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1.13 multiplied by the area without
overlap). The take estimates were
calculated without overlap. The 160 dB
radii are based on acoustic modeling
data for the airguns that may be used
during the proposed action (see SIO’s
IHA application). During the proposed
low-energy seismic survey, the transect
lines are widely spaced relative to the
160 dB distance. As summarized in
Table 2 (see Table 1 and Figure 2 of the
IHA application), the modeling results
for the proposed low-energy seismic
airgun array indicate the received levels
are dependent on water depth. Since the
majority of the proposed airgun
operations would be conducted in
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waters 100 to 1,000 m deep or greater
than 1,000 m deep, the buffer zone of
600 m or 400 m, respectively, for the
two 45 in3 GI airguns was used.
The number of different individuals
potentially exposed to received levels
greater than or equal to 160 dB re 1 mPa
(rms) from seismic airgun operations
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 (excluding overlap).
The area expected to be ensonified
was determined by entering the planned
tracklines into MapInfo GIS using the
GIS to identify the relevant areas by
‘‘drawing’’ the applicable 160 dB (rms)
isopleth around each trackline, and then
calculating the total area within the
isopleth. Applying the approach
described above, approximately 1,153.6
km2 (including the 25% contingency
[approximately 923 km2 without
contingency]) would be ensonified
within the 160 dB isopleth for seismic
airgun operations on one or more
occasions during the proposed lowenergy seismic survey. The total
ensonified area (1,154 km2 [336.5 nmi2])
was calculated by adding 847 km2
(246.9 nmi2) in deep water, 76 km2 (22.2
nmi2), and 230.8 km2 (67.3 nmi2) for the
25% contingency. The take calculations
within the study sites do not explicitly
add animals to account for the fact that
new animals (i.e., turnover) not
accounted for in the initial density
snapshot could also approach and enter
the area ensonified above 160 dB for
seismic airgun operations. However,
studies suggest that many marine
mammals would avoid exposing
themselves to sounds at this level,
which suggests that there would not
necessarily be a large number of new
animals entering the area once the
seismic survey started. Because this
approach for calculating take estimates
does not account for turnover in the
marine mammal populations in the area
during the course of the proposed lowenergy seismic survey, the actual
number of individuals exposed may be
underestimated. However, any
underestimation is likely offset by the
conservative (i.e., probably
overestimated) line-kilometer distances
(including the 25% contingency) used
to calculate the survey area, and the fact
the approach assumes that no cetaceans
or pinnipeds would move away or
toward the tracklines as the Revelle
approaches in response to increasing
sound levels before the levels reach 160
dB for seismic airgun operations, which
is likely to occur and which would
decrease the density of marine
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mammals in the survey area. Another
way of interpreting the estimates in
Table 6 is that they represent the
number of individuals that would be
expected (in absence of a seismic
program) to occur in the waters that
would be exposed to greater than or
equal to 160 dB (rms) for seismic airgun
operations.
SIO’s estimates of exposures to
various sound levels assume that the
proposed low-energy seismic survey
would be carried out in full; however,
the ensonified areas calculated using the
planned number of line-kilometers has
been increased by 25% to accommodate
lines that may need to be repeated,
equipment testing, etc. As is typical
during offshore seismic surveys,
inclement weather and equipment
malfunctions would be likely to cause
delays and may limit the number of
useful line-kilometers of airgun
operations that can be undertaken. The
estimates of the numbers of marine
mammals potentially exposed to 160 dB
(rms) received levels are precautionary
and probably overestimate the actual
numbers of marine mammals that could
be involved. These estimates assume
that there would be no weather,
equipment, or mitigation delays that
limit the airgun operations, which is
highly unlikely.
Table 5 shows the estimates of the
number of different individual marine
mammals anticipated to be exposed to
greater than or equal to 160 dB re 1 mPa
(rms) for seismic airgun operations
during the low-energy seismic survey if
no animals moved away from the survey
vessel. The total proposed take
authorization is given in the column
that is fourth from the left of Table 5.
Encouraging and Coordinating
Research
SIO and NSF would coordinate the
planned marine mammal monitoring
program associated with the proposed
low-energy seismic survey with other
parties that express interest in this
activity and area. SIO and NSF would
coordinate with applicable U.S.
agencies (e.g., NMFS) and the
government of New Zealand, and would
comply with their requirements. The
proposed low-energy seismic survey
falls under Level 3 of the ‘‘Code of
Conduct for minimizing acoustic
disturbance to marine mammals from
seismic survey operations’’ issued by
New Zealand. Level 3 seismic surveys
are exempt from the provisions of the
Code of Conduct.
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Impact on Availability of Affected
Species or Stock for Taking for
Subsistence Uses
Section 101(a)(5)(D) of the MMPA
also requires NMFS to determine that
the authorization would not have an
unmitigable adverse impact on the
availability of marine mammal species
or stocks for subsistence use. There are
no relevant subsistence uses of marine
mammals implicated by this action (in
the Southwest Pacific Ocean, East of
New Zealand study area). Therefore,
NMFS has determined that the total
taking of affected species or stocks
would not have an unmitigable adverse
impact on the availability of such
species or stocks for taking for
subsistence purposes.
Analysis and Preliminary
Determinations
Negligible Impact
Negligible impact is ‘‘an impact
resulting from the specified activity that
cannot be reasonably expected to, and is
not reasonably likely to, adversely affect
the species or stock through effects on
annual rates of recruitment or survival’’
(50 CFR 216.103). A negligible impact
finding is based on the lack of likely
adverse effects on annual rates of
recruitment or survival (i.e., populationlevel effects). An estimate of the number
of Level B harassment takes, alone, is
not enough information on which to
base an impact determination. In
addition to considering estimates of the
number of marine mammals that might
be ‘‘taken’’ through behavioral
harassment, NMFS must consider other
factors, such as the likely nature of any
responses (their intensity, duration, etc.)
and the context of any responses
(critical reproductive time or location,
migration, etc.), as well as the number
and nature of estimated Level A
harassment takes, the number of
estimated mortalities, effects on habitat,
and the status of the species.
In making a negligible impact
determination, NMFS evaluated factors
such as:
(1) The number of anticipated serious
injuries and or mortalities;
(2) The number and nature of
anticipated injuries;
(3) The number, nature, intensity, and
duration of takes by Level B harassment
(all of which are relatively limited in
this case);
(4) The context in which the takes
occur (e.g., 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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(5) 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);
(6) Impacts on habitat affecting rates
of recruitment/survival; and
(7) The effectiveness of monitoring
and mitigation measures.
NMFS has preliminarily determined
that the specified activities associated
with the marine seismic survey are not
likely to cause PTS, or other (nonauditory) injury, serious injury, or
death, based on the analysis above and
the following factors:
(1) The likelihood that, given
sufficient notice through relatively slow
ship speed, marine mammals are
expected to move away from a noise
source that is annoying prior to its
becoming potentially injurious;
(2) The availability of alternate areas
of similar habitat value for marine
mammals to temporarily vacate the
survey area during the operation of the
airgun(s) to avoid acoustic harassment;
(3) The potential for temporary or
permanent hearing impairment is
relatively low and would likely be
avoided through the implementation of
the required monitoring and mitigation
measures (including shut-down
measures); and
(4) The likelihood that marine
mammal detection ability by trained
PSOs is high at close proximity to the
vessel.
No injuries, serious injuries, or
mortalities are anticipated to occur as a
result of the SIO’s planned low-energy
seismic survey, and none are proposed
to be authorized by NMFS. Table 5 of
this document outlines the number of
requested Level B harassment takes that
are anticipated as a result of these
activities. Due to the nature, degree, and
context of Level B (behavioral)
harassment anticipated and described in
this notice (see ‘‘Potential Effects on
Marine Mammals’’ section above), the
activity is not expected to impact rates
of annual recruitment or survival for
any affected species or stock,
particularly given NMFS’s and the
applicant’s proposed mitigation,
monitoring, and reporting measures to
minimize impacts to marine mammals.
Additionally, the low-energy seismic
survey 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 hr
cycle). Behavioral reactions to noise
exposure (such as disruption of critical
life functions, displacement, or
avoidance of important habitat) are
more likely to be significant if they last
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more than one diel cycle or recur on
subsequent days (Southall et al., 2007).
While airgun operations are anticipated
to occur on consecutive days, the
estimated duration of the survey would
not last more than a total of
approximately 27 operational days.
Additionally, the low-energy 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, so individual animals
likely would only be exposed to and
harassed by sound for less than a day.
As mentioned previously, NMFS
estimates that 32 species of marine
mammals under its jurisdiction could be
potentially affected by Level B
harassment over the course of the IHA.
The population estimates for the marine
mammal species that may be taken by
Level B harassment were provided in
Table 3 and 5 of this document. As
shown in those tables, the proposed
takes represent small proportions of the
overall populations of these marine
mammal species where abundance
estimates are available (i.e., less than
1%).
Of the 32 marine mammal species
under NMFS jurisdiction that may or
are known to likely occur in the study
area, six are listed as threatened or
endangered under the ESA: Southern
right, humpback, sei, fin, blue, and
sperm whales. These species are also
considered depleted under the MMPA.
None of the other marine mammal
species that may be taken are listed as
depleted under the MMPA. Of the ESAlisted species, incidental take has been
requested to be authorized for six
species. As mitigation to reduce impacts
to the affected species or stocks, SIO
would be required to cease airgun
operations if any marine mammal enters
designated exclusion zones. No injury,
serious injury, or mortality is expected
to occur for any of these species, and
due to the nature, degree, and context of
the Level B harassment anticipated, and
the activity is not expected to impact
rates of recruitment or survival for any
of these species.
NMFS has preliminarily determined
that, provided that the aforementioned
mitigation and monitoring measures are
implemented, the impact of conducting
a low-energy marine seismic survey in
the Southwest Pacific Ocean, May to
June 2015, may result, at worst, in a
modification in behavior and/or lowlevel physiological effects (Level B
harassment) of certain species of marine
mammals.
While behavioral modifications,
including temporarily vacating the area
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15093
during the operation of the airgun(s),
may be made by these species to avoid
the resultant acoustic disturbance, the
availability of alternate areas for species
to move to and the short and sporadic
duration of the research activities, have
led NMFS to preliminary determine that
the taking by Level B harassment from
the specified activity would have a
negligible impact on the affected species
in the specified geographic region. Due
to the nature, degree, and context of
Level B (behavioral) harassment
anticipated and described (see
‘‘Potential Effects on Marine Mammals’’
section above) in this notice, the
proposed activity is not expected to
impact rates of annual recruitment or
survival for any affected species or
stock, particularly given the NMFS and
applicant’s proposal to implement
mitigation and monitoring measures
would minimize impacts to marine
mammals. 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 proposed monitoring and
mitigation measures, NMFS
preliminarily finds that the total marine
mammal take from SIO’s proposed lowenergy seismic survey would have a
negligible impact on the affected marine
mammal species or stocks.
Small Numbers
As mentioned previously, NMFS
estimates that 32 species of marine
mammals under its jurisdiction could be
potentially affected by Level B
harassment over the course of the IHA.
The population estimates for the marine
mammal species that may be taken by
Level B harassment were provided in
Tables 3 and 5 of this document.
The estimated numbers of individual
cetaceans and pinnipeds that could be
exposed to seismic sounds with
received levels greater than or equal to
160 dB re 1 mPa (rms) during the
proposed low-energy seismic survey
(including a 25% contingency) are in
Table 5 of this document. Of the
cetaceans, 2 southern right, 2 pygmy
right, 2 humpback, 2 Antarctic minke, 2
minke, 2 Bryde’s, 2 sei, 2 fin, 2 blue,
and 10 sperm whales could be taken by
Level B harassment during the proposed
low-energy seismic survey, which
would represent 0.03, unknown, 0.1,
less than 0.01, less than 0.01, less than
0.01, less than 0.01, less than 0.01, 0.03,
and 0.03% of the affected worldwide or
regional populations, respectively. In
addition, 5 pygmy sperm, 2 Cuvier’s
beaked, 3 Shepherd’s beaked, 2
southern bottlenose, 2 Andrew’s beaked,
2 Blainville’s beaked, 2 Gray’s beaked,
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2 Hector’s beaked, 2 spade-toothed
beaked, and 3 strap-toothed beaked
could be taken be Level B harassment
during the proposed low-energy seismic
survey, which would represent
unknown, less than 0.01, less than 0.01,
less than 0.01, less than 0.01, less than
0.01, less than 0.01, less than 0.01, less
than 0.01, and less than 0.01% of the
affected worldwide or regional
populations, respectively. Of the
delphinids, 12 killer whales, 10 false
killer whales, 20 long-finned pilot
whales, 20 short-finned pilot whales, 95
bottlenose dolphins, 95 dusky dolphins,
38 Hector’s dolphins, 57 hourglass
dolphins, 189 short-beaked common
dolphins, and 57 southern right whale
dolphins could be taken by Level B
harassment during the proposed lowenergy seismic survey, which would
represent 0.02, unknown, 0.01, less than
0.01, 0.02, 0.79, 0.51, 0.04, less than
0.01, and unknown of the affected
worldwide or regional populations,
respectively. Of the pinnipeds, 15 New
Zealand fur seals and 6 southern
elephant seals could be taken by Level
B harassment during the proposed lowenergy seismic survey, which would
represent 0.01 and less than 0.01 of the
affected worldwide or regional
population, respectively.
No known current worldwide or
regional population estimates are
available for 4 species under NMFS’s
jurisdiction that could potentially be
affected by Level B harassment over the
course of the IHA. These species are the
pygmy right, pygmy sperm, and false
killer whales and southern right whale
dolphins. Pygmy right whales have a
circumglobal distribution and occur
throughout coastal and oceanic waters
in the Southern Hemisphere (between
30 to 55° South) (Jefferson et al., 2008).
Pygmy sperm whales occur in deep
waters on the outer continental shelf
and slope in tropical to temperate
waters of the Atlantic, Indian, and
Pacific Oceans. False killer whales
generally occur in deep offshore tropical
to temperate waters (between 50° North
to 50° South) of the Atlantic, Indian,
and Pacific Oceans (Jefferson et al.,
2008). Southern right whale dolphins
have a circumpolar distribution and
generally occur in deep temperate to
sub-Antarctic waters in the Southern
Hemisphere (between 30 to 65° South)
(Jefferson et al., 2008). Based on these
distributions and preferences of these
species, NMFS concludes that the
requested take of these species likely
represent small numbers relative to the
affected species’ overall population
sizes.
NMFS makes its small numbers
determination based on the numbers of
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marine mammals that would be taken
relative to the populations of the
affected species or stocks. The proposed
take estimates all represent small
numbers relative to the affected species
or stock size (i.e., all are less than 1%),
with the exception of the four species
(i.e., pygmy right, pygmy sperm, and
false killer whales and southern right
whale dolphins) for which a qualitative
rationale was provided.
Endangered Species Act
Of the species of marine mammals
that may occur in the proposed survey
area, six are listed as endangered under
the ESA: The southern right, humpback,
sei, fin, blue, and sperm whales. Under
section 7 of the ESA, NSF, on behalf of
SIO, has initiated formal consultation
with the NMFS, Office of Protected
Resources, Endangered Species Act
Interagency Cooperation Division, on
this proposed low-energy seismic
survey. NMFS’s Office of Protected
Resources, Permits and Conservation
Division, has initiated formal
consultation under section 7 of the ESA
with NMFS’s Office of Protected
Resources, Endangered Species Act
Interagency Cooperation Division, to
obtain a Biological Opinion evaluating
the effects of issuing the IHA on
threatened and endangered marine
mammals and, if appropriate,
authorizing incidental take. NMFS
would conclude formal section 7
consultation prior to making a
determination on whether or not to
issue the IHA. If the IHA is issued, in
addition to the mitigation and
monitoring requirements included in
the IHA, NSF and SIO would be
required to comply with the Terms and
Conditions of the Incidental Take
Statement corresponding to NMFS’s
Biological Opinion issued to both NSF
and SIO, and NMFS’s Office of
Protected Resources.
National Environmental Policy Act
With SIO’s complete IHA application,
NSF and SIO provided NMFS a ‘‘Draft
Environmental Analysis of a LowEnergy Marine Geophysical Survey by
the R/V Roger Revelle in the Southwest
Pacific Ocean, East of New Zealand,
May to June 2015,’’ (Draft
Environmental Analysis), prepared by
LGL Limited, Environmental Research
Associates, on behalf of NSF and SIO.
The Draft Environmental Analysis
analyzes the direct, indirect, and
cumulative environmental impacts of
the proposed specified activities on
marine mammals, including those listed
as threatened or endangered under the
ESA. NMFS, after independently
reviewing and evaluating the document
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for sufficiency and compliance with
Council on Environmental Quality
(CEQ) NEPA regulations and NOAA
Administrative Order 216–6 § 5.09(d),
will conduct a separate NEPA analysis
and prepare a ‘‘Draft Environmental
Assessment on the Issuance of an
Incidental Harassment Authorization to
the Scripps Institution of Oceanography
to Take Marine Mammals by
Harassment Incidental to a Low-Energy
Marine Geophysical Survey in the
Southwest Pacific Ocean, East of New
Zealand, May to June 2015,’’ and decide
whether to sign a Finding of No
Significant Impact (FONSI), prior to
making a determination on the issuance
of the IHA.
Proposed Authorization
As a result of these preliminary
determinations, NMFS proposes to issue
an IHA to SIO for conducting the lowenergy seismic survey in the Southwest
Pacific Ocean, East of New Zealand,
provided the previously mentioned
mitigation, monitoring, and reporting
requirements are incorporated. This
section contains a draft of the IHA itself.
The wording contained in this section is
proposed for inclusion in the IHA (if
issued). The proposed IHA language is
provided below:
The NMFS hereby authorizes the
Scripps Institution of Oceanography,
8602 La Jolla Shores Drive, La Jolla,
California 92037, under section
101(a)(5)(D) of the Marine Mammal
Protection Act (MMPA) (16 U.S.C.
1371(a)(5)(D)), to harass small numbers
of marine mammals incidental to a lowenergy marine geophysical (seismic)
survey conducted by the R/V Roger
Revelle (Revelle) in the Southwest
Pacific Ocean, East of New Zealand,
May to June 2015:
1. Effective Dates
This Authorization is valid from May
18, 2015 through July 30, 2015.
2. Specified Activity and Geographic
Region
This Authorization is valid only for
SIO’s activities associated with lowenergy seismic survey, bathymetric
profile, and heat-flow probe
measurements conducted aboard the
Revelle that shall occur in the following
specified geographic area:
(a) In selected regions of the
Southwest Pacific Ocean off the east
coast of New Zealand. The survey sites
are located in the Exclusive Economic
Zone, outside of territorial waters
(located between approximately 38.5
and 42.5° South, and between 174 and
180° East). Water depths in the survey
area are expected to be approximately
200 to 3,000 m. No airgun operations
would occur in shallow (less than 100
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m) water depths. Airgun operations
would take approximately 135 hours in
total and 1,250 km, and the remainder
of the time would be spent in transit
and collecting heat-flow measurements
and sediment core samples. The lowenergy seismic survey would be
conducted as specified in SIO’s IHA
application and the associated NSF and
SIO Environmental Analysis.
3. This Authorization does not permit
incidental takes of marine mammals in
the territorial sea of foreign nations, as
the MMPA does not apply in those
waters. The territorial sea extends at the
most 22.2 kilometers (km) (12 nautical
miles [nmi]) from the baseline of a
coastal State.
4. Species Authorized and Level of
Takes
(a) The incidental taking of marine
mammals, by Level B harassment only,
is limited to the following species in the
waters of the Southwest Pacific Ocean,
East of New Zealand:
(i) Mysticetes—see Table 5 (above) for
authorized species and take numbers.
(ii) Odontocetes—see Table 5 (above)
for authorized species and take
numbers.
(iii) Pinnipeds—see Table 5 (above)
for authorized species and take
numbers.
(iv) If any marine mammal species are
encountered during seismic activities
that are not listed in Table 5 (above) for
authorized taking and are likely to be
exposed to sound pressure levels (SPLs)
greater than or equal to 160 dB re 1 mPa
(rms) for seismic airgun operations, then
the SIO must alter speed or course or
shut-down the airguns to prevent take.
(b) The taking by injury (Level A
harassment), serious injury, or death of
any of the species listed in Condition
4(a) above or the taking of any kind of
any other species of marine mammal is
prohibited and may result in the
modification, suspension, or revocation
of this Authorization.
5. The sources authorized for taking
by Level B harassment are limited to the
following acoustic sources, absent an
amendment to this Authorization:
A two Generator Injector (GI) airgun
array (each with a discharge volume of
45 cubic inches [in3]) with a total
volume of 90 in3 (or smaller).
6. Prohibited Take
The taking of any marine mammal in
a manner prohibited under this
Authorization must be reported
immediately to the Office of Protected
Resources, National Marine Fisheries
Service (NMFS), at 301–427–8401.
7. Mitigation and Monitoring
Requirements
The SIO is required to implement the
following mitigation and related
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15095
monitoring requirements when
conducting the specified activities to
achieve the least practicable impact on
affected marine mammal species or
stocks:
for pinnipeds before the two GI airgun
array (90 in3 total volume) is in
operation. See Table 2 (above) for
distances and buffer and exclusion
zones.
Protected Species Observers and Visual
Monitoring
(a) Utilize at least one NMFSqualified, vessel-based Protected
Species Observer (PSO) to visually
watch for and monitor marine mammals
near the seismic source vessel during
daylight airgun operations (from
nautical twilight-dawn to nautical
twilight-dusk) and before and during
ramp-ups of airguns day or night. Three
PSOs shall be based onboard the vessel.
(i) The Revelle’s vessel crew shall also
assist in detecting marine mammals,
when practicable.
(ii) PSOs shall have access to reticle
binoculars (7 x 50 Fujinon) equipped
with a built-in daylight compass and
range reticles, big-eye binoculars (25 x
150), optical range finders, and nightvision devices.
(iii) PSO shifts shall last no longer
than 4 hours at a time.
(iv) PSO(s) shall also make
observations during daylight periods
when the seismic airguns are not
operating, when feasible, for
comparison of animal abundance and
behavior.
(v) PSO(s) shall conduct monitoring
while the airgun array and streamer(s)
are being deployed or recovered from
the water.
(b) PSO(s) shall record the following
information when a marine mammal is
sighted:
(i) 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
including responses to ramp-up), and
behavioral pace; and
(ii) Time, location, heading, speed,
activity of the vessel (including number
of airguns operating and whether in
state of ramp-up or shut-down),
Beaufort sea state and wind force,
visibility, and sun glare; and
(iii) The data listed under Condition
7(b)(ii) shall also be recorded at the start
and end of each observation watch and
during a watch whenever there is a
change in one or more of the variables.
Visual Monitoring at the Start of the
Airgun Operations
Buffer and Exclusion Zones
(c) Establish a 160 dB re 1 m Pa (rms)
buffer zone, as well as a180 dB re 1 m Pa
(rms) exclusion zone for cetaceans and
a 190 dB re 1 m Pa (rms) exclusion zone
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(d) Visually observe the entire extent
of the exclusion zone (180 dB re 1 m Pa
[rms] for cetaceans and 190 dB re 1 m Pa
[rms] for pinnipeds; see Table 2 [above]
for distances) using two NMFS-qualified
PSOs, for at least 30 minutes prior to
starting the airgun array (day or night).
(i) If the PSO(s) sees a marine
mammal within the exclusion zone, SIO
must delay the seismic survey until the
marine mammal(s) has left the area. If
the PSO(s) sees a marine mammal that
surfaces, then dives below the surface,
the PSO(s) shall continue to observe the
exclusion zone for 30 minutes, and if
the PSO sees no marine mammals
during that time, the PSO should
assume that the animal has moved
beyond the exclusion zone.
(ii) If for any reason the entire radius
cannot be seen for the entire 30 minutes
(i.e., rough seas, fog, darkness), or if
marine mammals are near, approaching,
or in the exclusion zone, the airguns
may not be ramped-up. If one airgun is
already running at a source level of at
least 180 dB re 1 m Pa (rms), SIO may
start the second airgun without
observing the entire exclusion zone for
30 minutes prior, provided no marine
mammals are known to be near the
exclusion zone (in accordance with
Condition 7[e] below).
Ramp-Up Procedures
(e) Implement a ‘‘ramp-up’’
procedure, which means starting with a
single GI airgun and adding a second GI
airgun after five minutes, when starting
up at the beginning of seismic
operations or anytime after the entire
array has been shut-down for more than
15 minutes. During ramp-up, the two
PSOs shall monitor the exclusion zone,
and if marine mammals are sighted, a
shut-down shall be implemented as
though the full array (both GI airguns)
were operational. Therefore, initiation
of ramp-up procedures from shut-down
requires that the two PSOs be able to
view the full exclusion zone as
described in Condition 7(d) (above).
Shut-Down Procedures
(f) Shut-down the airgun(s) if a marine
mammal is detected within, approaches,
or enters the relevant exclusion zone (as
defined in Table 2, above). A shut-down
means all operating airguns are shutdown (i.e., turned off).
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(g) Following a shut-down, the airgun
activity shall not resume until the
PSO(s) has visually observed the marine
mammal(s) exiting the exclusion zone
and determined it is not likely to return,
or has not seen the marine mammal
within the exclusion zone for 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,
dwarf and pygmy sperm, killer, and
beaked whales).
(h) Following a shut-down and
subsequent animal departure, airgun
operations may resume, following the
ramp-up procedures described in
Condition 7(e).
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Speed or Course Alteration
(i) Alter speed or course during
seismic operations if a marine mammal,
based on its position and relative
motion, appears likely to enter the
relevant exclusion zone. If speed or
course alteration is not safe or
practicable, or if after alteration the
marine mammal still appears likely to
enter the exclusion zone, further
mitigation measures, such as a shutdown, shall be taken.
Survey Operations During Low-Light
Hours
(j) Marine seismic surveying may
continue into low-light hours if such
segment(s) of the survey is initiated
when the entire relevant exclusion
zones are visible and can be effectively
monitored.
(k) No initiation of airgun array
operations is permitted from a shutdown position during low-light hours
(such as in dense fog or heavy rain)
when the entire relevant exclusion zone
cannot be effectively monitored by the
PSO(s) on duty.
(l) To the maximum extent
practicable, schedule seismic operations
(i.e., shooting airguns) during daylight
hours, and heat-flow measurements at
nighttime hours.
8. Reporting Requirements
SIO are required to:
(a) Submit a draft report on all
activities and monitoring results to the
Office of Protected Resources, NMFS,
within 90 days of the completion of the
Revelle’s Southwest Pacific Ocean, East
of New Zealand cruise. This report must
contain and summarize the following
information:
(i) Dates, times, locations, heading,
speed, weather, sea conditions
(including Beaufort sea state and wind
force), and associated activities during
all seismic operations and marine
mammal sightings;
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(ii) Species, number, location,
distance from the vessel, and behavior
of any marine mammals, as well as
associated seismic activity (e.g., number
of shut-downs), observed throughout all
monitoring activities.
(iii) An estimate of the number (by
species) of marine mammals that: (A)
Are known to have been exposed to the
seismic activity (based on visual
observation) at received levels greater
than or equal to 160 dB re 1 mPa (rms)
(for seismic airgun operations), and/or
180 dB re 1 mPa (rms) for cetaceans and
190 dB re 1 mPa (rms) for pinnipeds,
with a discussion of any specific
behaviors those individuals exhibited;
and (B) may have been exposed (based
on modeled values for the two GI airgun
array) to the seismic activity at received
levels greater than or equal to 160 dB re
1 mPa (rms) (for seismic airgun
operations), and/or 180 dB re 1 mPa
(rms) for cetaceans and 190 dB re 1 mPa
(rms) for pinnipeds, with a discussion of
the nature of the probable consequences
of that exposure on the individuals that
have been exposed.
(iv) A description of the
implementation and effectiveness of the:
(A) Terms and Conditions of the
Biological Opinion’s Incidental Take
Statement (ITS) (attached); and (B)
mitigation measures of the IHA. For the
Biological Opinion, the report shall
confirm the implementation of each
Term and Condition, as well as any
conservation recommendations, and
describe their effectiveness, for
minimizing the adverse effects of the
action on Endangered Species Act-listed
marine mammals.
(b) Submit a final report to the Chief,
Permits and Conservation Division,
Office of Protected Resources, NMFS,
within 30 days after receiving comments
from NMFS on the draft report. If NMFS
decides that the draft report needs no
comments, the draft report shall be
considered to be the final report.
8. Reporting Prohibited Take
(a) (i) In the unanticipated event that
the specified activity clearly causes the
take of a marine mammal in a manner
prohibited by this Authorization, such
as an injury (Level A harassment),
serious injury or mortality (e.g., through
ship-strike, gear interaction, and/or
entanglement), SIO shall immediately
cease the specified activities and
immediately report the incident to the
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS, at 301–427–8401 and/or by
email to Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov. The report
must include the following information:
(ii) Time, date, and location (latitude/
longitude) of the incident; the name and
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type of vessel involved; the 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 marine mammal
observations in the 24 hours preceding
the incident; species identification or
description of the animal(s) involved;
the fate of the animal(s); and
photographs or video footage of the
animal (if equipment is available).
Activities shall not resume until
NMFS is able to review the
circumstances of the prohibited take.
NMFS shall work with SIO to determine
what is necessary to minimize the
likelihood of further prohibited take and
ensure MMPA compliance. SIO may not
resume their activities until notified by
NMFS via letter, email, or telephone.
Reporting an Injured or Dead Marine
Mammal With an Unknown Cause of
Death
(b) In the event that SIO discover an
injured or dead marine mammal, and
the lead PSO determines that the cause
of the injury or death is unknown and
the death is relatively recent (i.e., in less
than a moderate state of decomposition),
SIO shall immediately report the
incident to the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, at 301–
427–8401, and/or by email to
Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov. The report
must include the same information
identified in Condition 8(c)(i) above.
Activities may continue while NMFS
reviews the circumstances of the
incident. NMFS shall work with SIO to
determine whether modifications in the
activities are appropriate.
Reporting an Injured or Dead Marine
Mammal Not Related to the Activities
(c) In the event that SIO discovers an
injured or dead marine mammal, and
the lead PSO determines that the injury
or death is not associated with or related
to the activities authorized in Condition
2 of this Authorization (e.g., previously
wounded animal, carcass with moderate
to advanced decomposition, or
scavenger damage), SIO shall report the
incident to the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, at 301–
427–8401, and/or by email to
Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov, within 24
hours of the discovery. SIO shall
provide photographs or video footage (if
available) or other documentation of the
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stranded animal sighting to NMFS.
Activities may continue while NMFS
reviews the circumstances of the
incident.
9. Endangered Species Act Biological
Opinion and Incidental Take Statement
(a) SIO is required to comply with the
Terms and Conditions of the ITS
corresponding to NMFS’s Biological
Opinion issued to both NSF and SIO,
and NMFS’s Office of Protected
Resources.
(b) A copy of this Authorization and
the ITS must be in the possession of all
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contractors and PSO(s) operating under
the authority of this Incidental
Harassment Authorization.
Request for Public Comments
NMFS requests comment on our
analysis, the draft authorization, and
any other aspect of the notice of the
proposed IHA for SIO’s low-energy
seismic survey. Please include with
your comments any supporting data or
literature citations to help inform our
final decision on SIO’s request for an
MMPA authorization. Concurrent with
PO 00000
Frm 00039
Fmt 4701
Sfmt 9990
15097
the publication of this notice in the
NMFS is forwarding
copies of this application to the Marine
Mammal Commission and its
Committee of Scientific Advisors.
FEDERAL REGISTER,
Dated: March 12, 2015.
Perry Gayaldo,
Deputy Director, Office of Protected
Resources, National Marine Fisheries Service.
[FR Doc. 2015–06261 Filed 3–19–15; 8:45 am]
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Agencies
[Federal Register Volume 80, Number 54 (Friday, March 20, 2015)]
[Notices]
[Pages 15059-15097]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-06261]
[[Page 15059]]
Vol. 80
Friday,
No. 54
March 20, 2015
Part II
Department of Commerce
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National Oceanic and Atmospheric Administration
Takes of Marine Mammals Incidental to Specified Activities; Low-Energy
Marine Geophysical Survey in the Southwest Pacific Ocean, East of New
Zealand, May to June 2015; Notice
Federal Register / Vol. 80 , No. 54 / Friday, March 20, 2015 /
Notices
[[Page 15060]]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XD727
Takes of Marine Mammals Incidental to Specified Activities; Low-
Energy Marine Geophysical Survey in the Southwest Pacific Ocean, East
of New Zealand, May to June 2015
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed Incidental Harassment Authorization; request
for comments.
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SUMMARY: NMFS has received an application from the Scripps Institution
of Oceanography (SIO), on behalf of SIO and the U.S. National Science
Foundation (NSF), for an Incidental Harassment Authorization (IHA) to
take marine mammals, by harassment, incidental to conducting a low-
energy marine geophysical (seismic) survey in the Southwest Pacific
Ocean, East of New Zealand, May to June 2015. Pursuant to the Marine
Mammal Protection Act (MMPA), NMFS is requesting comments on its
proposal to issue an IHA to SIO to incidentally harass, by Level B
harassment only, 32 species of marine mammals during the specified
activity.
DATES: Comments and information must be received no later than April
20, 2015.
ADDRESSES: Comments on the application should be addressed to Jolie
Harrison, Chief, Permits and Conservation Division, Office of Protected
Resources, National Marine Fisheries Service, 1315 East-West Highway,
Silver Spring, MD 20910. The mailbox address for providing email
comments is ITP.Goldstein@noaa.gov. Please include 0648-XD727 in the
subject line. NMFS is not responsible for email comments sent to
addresses other than the one provided here. Comments sent via email,
including all attachments, must not exceed a 25-megabyte file size.
Instructions: All comments received are a part of the public record
and will generally be posted to: https://www.nmfs.noaa.gov/pr/permits/incidental/ without change. All Personal Identifying Information (for
example, name, address, etc.) voluntarily submitted by the commenter
may be publicly accessible. Do not submit Confidential Business
Information or otherwise sensitive or protected information.
A copy of the IHA application may be obtained by writing to the
address specified above, telephoning the contact listed here (see FOR
FURTHER INFORMATION CONTACT) or visiting the Internet at: https://www.nmfs.noaa.gov/pr/permits/incidental/. Documents cited in this
notice may also be viewed by appointment, during regular business
hours, at the aforementioned address.
A ``Draft Environmental Analysis of a Low-Energy Marine Geophysical
Survey by the R/V Roger Revelle in the Southwest Pacific Ocean, East of
New Zealand, May to June 2015'' (Draft Environmental Analysis) in
accordance with the National Environmental Policy Act (NEPA) and the
regulations published by the Council of Environmental Quality (CEQ),
has been prepared on behalf of NSF and SIO. It is posted at the
foregoing site. NMFS has independently evaluated the Draft
Environmental Analysis and has prepared a separate NEPA analysis titled
``Draft Environmental Assessment on the Issuance of an Incidental
Harassment Authorization to the Scripps Institution of Oceanography to
Take Marine Mammals by Harassment Incidental to a Low-Energy Marine
Geophysical Survey in the Southwest Pacific Ocean, East of New Zealand,
May to June 2015.'' Information in the SIO's IHA application, Draft
Environmental Analysis, Draft EA and this notice of the proposed IHA
collectively provide the environmental information related to proposed
issuance of the IHA for public review and comment. NMFS will review all
comments submitted in response to this notice as we complete the NEPA
process, including a decision of whether to sign a Finding of No
Significant Impact (FONSI), prior to a final decision on the IHA
request.
FOR FURTHER INFORMATION CONTACT: Howard Goldstein or Jolie Harrison,
Office of Protected Resources, NMFS, 301-427-8401.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the MMPA, (16 U.S.C. 1361 et seq.)
direct the Secretary of Commerce (Secretary) to allow, upon request,
the incidental, but not intentional, taking of small numbers of marine
mammals by United States citizens who engage in a specified activity
(other than commercial fishing) within a specified geographical region
if certain findings are made and either regulations are issued or, if
the taking is limited to harassment, a notice of a proposed
authorization is provided to the public for review.
An authorization for incidental takings shall be granted if NMFS
finds that the taking will have a negligible impact on the species or
stock(s), will not have an unmitigable adverse impact on the
availability of the species or stock(s) for subsistence uses (where
relevant), and if the permissible methods of taking and requirements
pertaining to the mitigation, monitoring and reporting of such takings
are set forth. NMFS has defined ``negligible impact'' in 50 CFR 216.103
as ``. . . an impact resulting from the specified activity that cannot
be reasonably expected to, and is not reasonably likely to, adversely
affect the species or stock through effects on annual rates of
recruitment or survival.''
Section 101(a)(5)(D) of the MMPA established an expedited process
by which citizens of the United States can apply for an authorization
to incidentally take small numbers of marine mammals by harassment.
Section 101(a)(5)(D) of the MMPA establishes a 45-day time limit for
NMFS's review of an application, followed by a 30-day public notice and
comment period on any proposed authorizations for the incidental
harassment of small numbers of marine mammals. Within 45 days of the
close of the public comment period, NMFS must either issue or deny the
authorization.
Except with respect to certain activities not pertinent here, the
MMPA defines ``harassment'' as: any act of pursuit, torment, or
annoyance which (i) has the potential to injure a marine mammal or
marine mammal stock in the wild [Level A harassment]; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment].
Summary of Request
On December 15, 2014, NMFS received an application from SIO, on
behalf of SIO and NSF, requesting that NMFS issue an IHA for the take,
by Level B harassment only, of small numbers of marine mammals
incidental to conducting a low-energy marine seismic survey as well as
heat-flow measurements in the Southwest Pacific Ocean, at three sites
off the east coast of New Zealand, during May to June 2015. The
sediment coring component of the proposed project, which was described
in the IHA application and Draft Environmental Analysis, was not funded
and no piston or gravity coring for seafloor samples would be
[[Page 15061]]
conducted during the low-energy seismic survey. The low-energy seismic
survey would take place within the Exclusive Economic Zone (EEZ) and
outside the territorial waters of New Zealand. On behalf of SIO, the
U.S. Department of State is seeking authorization from New Zealand for
clearance to work within the EEZ.
The research would be conducted by Oregon State University and
funded by the U.S. National Science Foundation (NSF). SIO plan to use
one source vessel, the R/V Roger Revelle (Revelle), and a seismic
airgun array and hydrophone streamer to collect seismic data in the
Southwest Pacific Ocean, East of New Zealand. SIO plans to use
conventional low-energy, seismic methodology to perform marine-based
studies in the Southwest Pacific Ocean (see Figure 1 of the IHA
application). The studies would involve a low-energy seismic survey and
heat-flow measurements from the seafloor to meet a number of research
goals. In addition to the proposed operations of the seismic airgun
array and hydrophone streamer, SIO intends to operate two additional
acoustical data acquisition systems--a multi-beam echosounder and sub-
bottom profiler continuously throughout the low-energy seismic survey.
Acoustic stimuli (i.e., increased underwater sound) generated
during the operation of the seismic airgun array have the potential to
cause behavioral disturbance for marine mammals in the proposed study
area. This is the principal means of marine mammal taking associated
with these activities, and SIO have requested an authorization to take
32 species of marine mammals by Level B harassment. Take is not
expected to result from the use of the multi-beam echosounder and sub-
bottom profiler, as the brief exposure of marine mammals to one pulse,
or small numbers of signals, to be generated by these instruments in
this particular case is not likely to result in the harassment of
marine mammals. Also, NMFS does not expect take to result from
collision with the source vessel because it is a single vessel moving
at a relatively slow, constant cruise speed of 5 knots ([kts]; 9.3
kilometers per hour [km/hr]; 5.8 miles per hour [mph]) during seismic
acquisition within the study area, for a relatively short period of
time (approximately 27 operational days). It is likely that any marine
mammal would be able to avoid the vessel.
Description of the Proposed Specified Activity
Overview
SIO proposes to use one source vessel, the Revelle, a two GI airgun
array and one hydrophone streamer to conduct the conventional seismic
survey as part of the NSF-funded research project ``Collaborative
Research: The Thermal Regime of the Hikurangi Subduction Zone and
Shallow Slow Slip Events, New Zealand.'' In addition to the airguns,
SIO intends to conduct a bathymetric survey and heat-flow measurements
at three sites off the southwest coast of North Island and northeast
coast of South Island, New Zealand from the Revelle during the proposed
low-energy seismic survey.
Proposed Dates and Duration
The Revelle is expected to depart from Auckland, New Zealand on
approximately May 18, 2015 and arrive at Napier, New Zealand on
approximately June 18, 2015. Airgun operations would take approximately
135 hours in total, and the remainder of the time would be spent in
transit and collecting heat-flow measurements and cores. The total
distance the Revelle would travel in the region to conduct the proposed
research activities (i.e., seismic survey, bathymetric survey, and
transit to heat-flow measurement locations) represents approximately
2,000 km (1,079.9 nmi). Some minor deviation from this schedule is
possible, depending on logistics and weather (e.g., the cruise may
depart earlier or be extended due to poor weather; or there could be
additional days of airgun operations if collected data are deemed to be
of substandard quality).
Proposed Specified Geographic Region
The proposed project and survey sites are located off the southeast
coast of North Island and northeast coast of the South Island, New
Zealand in selected regions of the Southwest Pacific Ocean. The
proposed survey sites are located between approximately 38.5 to
42.5[deg] South and approximately 174 to 180[deg] East off the east
coast of New Zealand, in the EEZ of New Zealand and outside of
territorial waters (see Figure 1 of the IHA Application). Water depths
in the study area are between approximately 200 to 3,000 m (656.2 to
9,842.5 ft). The proposed low-energy seismic survey would be collected
in a total of nine grids of intersecting lines of two sizes (see Figure
1 of the IHA application) at exact locations to be determined in the
field during May to June 2015. Figure 1 also illustrates the general
bathymetry of the proposed study area. The proposed low-energy seismic
survey would be within an area of approximately 1,154 km\2\ (336.5
nmi\2\). This estimate is based on the maximum number of kilometers for
the low-energy seismic survey (1,250 km) multiplied by the area
ensonified around the planned tracklines (2 x 0.6 km in intermediate
water depths and 2 x 0.4 km in deep water depths). The ensonified area
is based on the predicted rms radii (m) based on modeling and empirical
measurements (assuming 100% use of the two 45 in\3\ GI airguns in 100
to 1,000 m or greater than 1,000 m water depths), which was calculated
to be 600 m (1,968.5 ft) or 400 m (1,312.3 ft).
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Detailed Description of the Proposed Specified Activity
In support of a research project put forward by Oregon State
University (OSU) and to be funded by NSF, SIO proposes to conduct a
low-energy seismic survey in the Southwest Pacific Ocean, East of New
Zealand, from May to June 2015. In addition to the low-energy seismic
survey, scientific research activities would include conducting a
bathymetric profile survey of the seafloor using transducer-based
instruments such as a multi-beam echosounder and sub-bottom profiler;
and heat-flow measurements from the seafloor using various methods and
equipment at three sites off the southeast coast of North Island and
northeast coast of South Island, New Zealand. Water depths in the
survey area are approximately 200 to 3,000 meters (m) (656.2 to 9,842.5
feet [ft]).
[[Page 15063]]
The proposed low-energy seismic survey is scheduled to occur for a
total of approximately 135 hours over the course of the entire cruise,
which would be for approximately 27 operational days in May to June
2015. The proposed low-energy seismic survey would be conducted during
the day (from nautical twilight-dawn to nautical twilight-dusk) and
night, and for up to approximately 72 hours of continuous operations at
a time. The operation hours and survey length would include equipment
testing, ramp-up, line changes, and repeat coverage. Some minor
deviation from these dates would be possible, depending on logistics
and weather. The Principal Investigators are Dr. R. N. Harris and Dr.
A. Trehu of the OSU.
The proposed surveys would allow the development of a process-based
understanding of the thermal structure of the Hikurangi subduction
zone, and the expansion of this understanding by using regional
observations of gas hydrate-related bottom simulating reflections. To
achieve the proposed project's goals, the Principal Investigators
propose to collect low-energy, high-resolution multi-channel system
profiles, heat-flow measurements, and sediment cores along transects
seaward and landward of the Hikurangi deformation front. Heat-flow
measurements would be made in well-characterized sites, increasing the
number of publicly available heat-flow and thermal conductivity
measurements from this continental margin by two orders of magnitude.
Seismic survey data would be used to produce sediment structural maps
and seismic velocities to achieve the project objectives. Data from
sediment cores would detect and estimate the nature and sources of
fluid flow through high permeability pathways in the overriding plate
and along the subduction thrust; characterize the hydrocarbon and gas
hydrate system to assist with estimates of heat flow from Bottom
Simulating Reflectors (BSR)s, their role in slope stability, and fluid
source; and elucidate the response of microbes involved in carbon
cycling to changes in methane flux.
The low-energy seismic survey would be collected in a total of 9
grids of intersecting lines of two sizes (see Figure 1 of the IHA
application) at exact locations to be determined in the field. The
water depths would be very similar to those at the nominal survey
locations shown in Figure 1 of the IHA application. The northern and
middle sites off the North Island would be the primary study areas, and
the southern site off the South Island would be a contingency area that
would only be surveyed if time permits. SIO's calculations assume that
7 grids at the primary areas and two grids at the southern site would
be surveyed. The total trackline distance of the low-energy seismic
survey would be approximately 1,250 km (including the two South Island
contingency sites), almost all in water depths greater than 1,000 m.
The procedures to be used for the survey would be similar to those
used during previous low-energy seismic surveys by SIO and NSF and
would use conventional seismic methodology. The proposed survey would
involve one source vessel, the Revelle. SIO would deploy a two Sercel
Generator Injector (GI) airgun array (each with a discharge volume of
45 in\3\ [290.3 cm\3\], in one string, with a total volume of 90 in\3\
[580.6 cm\3\]) as an energy source, at a tow depth of up to 2 m (6.6
ft) below the surface (more information on the airguns can be found in
SIO's IHA application). The airguns in the array would be spaced
approximately 8 m (26.2 ft) apart and 21 m (68.9 ft) astern of the
vessel. The receiving system would consist of one 600 m (1,968.5 ft)
long, 48-channel hydrophone streamer(s) towed behind the vessel. Data
acquisition is planned along a series of predetermined lines, almost
all (approximately 95%) of which would be in water depths greater than
1,000 m. As the GI airguns are towed along the survey lines, the
hydrophone streamer would receive the returning acoustic signals and
transfer the data to the onboard processing system. The seismic surveys
would be conducted while the heat-flow probe is being recharged. All
planned seismic data acquisition activities would be conducted by
technicians provided by SIO, with onboard assistance by the scientists
who have proposed the study. The vessel would be self-contained, and
the crew would live aboard the vessel for the entire cruise.
The planned seismic survey (including equipment testing, start-up,
line changes, repeat coverage of any areas, and equipment recovery)
would consist of approximately 1,250 kilometers (km) (674.9 nautical
miles [nmi]) of transect lines (including turns) in the study area in
the Southwest Pacific Ocean (see Figures 1 of the IHA application).
Approximately 95% of the low-energy seismic survey would occur in water
depths greater than 1,000 m. In addition to the operation of the airgun
array and heat-flow measurements, a multi-beam echosounder and a sub-
bottom profiler would also likely be operated from the Revelle
continuously throughout the cruise. There would be additional airgun
operations associated with equipment testing, ramp-up, and possible
line changes or repeat coverage of any areas where initial data quality
is sub-standard. In SIO's estimated take calculations, 25% has been
added for those additional operations.
Table 1--Proposed Low-Energy Seismic Survey Activities in the Southwest Pacific Ocean, East of New Zealand
----------------------------------------------------------------------------------------------------------------
Time between
Survey length (km) Total duration Airgun array airgun shots Streamer length (m)
(hr) \1\ total volume (distance)
----------------------------------------------------------------------------------------------------------------
1,250 (674.9 nmi)........... ~135 2 x 45 = 90 in\3\ 6 to 10 seconds 600 (1,968.5 ft)
(2 x 1474.8 (18.5 to 31 m or
cm\3\). 60.7 to 101.7
ft).
----------------------------------------------------------------------------------------------------------------
\1\ Airgun operations are planned for no more than approximately 72 continuous hours at a time.
Vessel Specifications
The Revelle, a research vessel owned by the U.S. Navy and operated
by SIO of the University of California San Diego, would tow the two GI
airgun array, as well as the hydrophone streamer. When the Revelle is
towing the airgun array and the relatively short hydrophone streamer,
the turning rate of the vessel while the gear is deployed is
approximately 20 degrees per minute, which is much higher than the
limit of 5 degrees per minute for a seismic vessel towing a streamer of
more typical length (much greater than 1 km [0.5 nmi]). Thus, the
maneuverability of the vessel would not be limited much during
operations with the streamer.
The U.S.-flagged vessel, built in 1996, has a length of 83 m (272.3
ft); a beam of 16.0 m (52.5 ft); a maximum draft of 5.2 m (19.5 ft);
and a gross tonnage of 3,180. The ship is powered by two 3,000
[[Page 15064]]
horsepower (hp) Propulsion General Electric motors) and a 1,180 hp
azimuthing jet bowthruster. The GI airgun compressor onboard the vessel
is manufactured by Price Air Compressors. The Revelle's operation speed
during seismic acquisition is typically approximately 9.3 km/hr (5 kts)
(varying between 7.4 to 11.1 km/hr [4 to 6 kts]). When not towing
seismic survey gear, the Revelle typically cruises at 22.2 to 23.1 km/
hr (12 to 12.5 kts) and has a maximum speed of 27.8 km/hr (15 kts). The
Revelle has an operating range of approximately 27,780 km (15,000 nmi)
(the distance the vessel can travel without refueling), which is
approximately 70 to 75 days. The vessel can accommodate 37 scientists
and 22 crew members.
The vessel also has two observation station locations from which
Protected Species Observers (PSO) would watch for marine mammals before
and during the proposed airgun operations on the Revelle. Observing
stations would be at the 02 level, with a PSO's eye level approximately
10.4 m (34 ft) above sea level--one forward on the 02 deck commanding a
forward-centered, approximately 240[deg] view around the vessel, and
one atop the aft hangar, with an aft-centered view that includes the
radii around the airguns. The eyes on the bridge watch would be at a
height of approximately 15 m (49 ft); PSOs would work on the enclosed
bridge and adjoining aft steering station during any inclement weather.
More details of the Revelle can be found in the IHA application and
online at: https://scripps.ucsd.edu/ships/revelle.
Acoustic Source Specifications--Seismic Airguns
The Revelle would deploy an airgun array, consisting of two 45
in\3\ Sercel GI airguns as the primary energy source and a 600 m
streamer(s) containing hydrophones. The airgun array would have a
supply firing pressure of 1,750 pounds per square inch (psi). Seismic
pulses for the GI airguns would be emitted at intervals of
approximately 6 to 10 seconds. There would be a maximum of
approximately 360 shots per hour. The number of shots per hour would
vary based upon the vessel speed over ground during the low-energy
seismic survey. During firing, a brief (approximately 20 millisecond)
pulse sound would be emitted; the airguns would be silent during the
intervening periods. The dominant frequency components would range from
0 to 188 Hertz (Hz).
The GI airguns would fire the compressed air volume in unison in
``true GI'' mode. The GI airguns would be used in ``true GI'' mode,
that is, the volume of the injector chamber (I) (105 in\3\ [1721
cm\3\]) of each GI airgun is greater to that of its generator chamber
(G) (45 in\3\ [737 cm\3\]) for each airgun. The generator chamber of
each GI airgun (45 in\3\) would be the primary source and the one
responsible for introducing the sound pulse into the ocean. The larger
(105 in\3\) injector chamber injects air into the previously-generated
bubble to maintain its shape, and would not introduce more sound into
the water. The two GI airguns would be spaced approximately 8 m (26.2
ft) apart, side-by-side, 21 m (68.9 ft) behind the Revelle, at a depth
of up to 2 m during the low-energy seismic survey.
The Nucleus modeling software used at Lamont-Doherty Earth
Observatory of Columbia University (L-DEO) does not include GI airguns
as part of its airgun library, however signatures and mitigation models
have been obtained for two 45 in\3\ G airguns that are close
approximations. For the two 45 in\3\ airgun array, the source output
(downward) is 230.6 dB re 1 [mu]Pam 0-to-peak and 235.8 dB re 1 [mu]Pam
for peak-to-peak. The dominant frequency range would be 0 to 188 Hz for
a pair of GI airguns towed at 2 m depth.
During the low-energy seismic survey, the vessel would attempt to
maintain a constant cruise speed of approximately 5 knots. The airguns
would operate continuously for no more than approximately 72 hours at a
time based on operational constraints. The total duration of the airgun
operations would not exceed 135 hours. The relatively short, 48-channel
hydrophone streamer would provide operational flexibility to allow the
low-energy seismic survey to proceed along the designated cruise
tracklines. The design of the seismic equipment is to achieve high-
resolution images with the ability to correlate to the ultra-high
frequency sub-bottom profiling data and provide cross-sectional views
to pair with the seafloor bathymetry.
Metrics Used in This Document
This section includes a brief explanation of the sound measurements
frequently used in the discussions of acoustic effects in this
document. Sound pressure is the sound force per unit area, and is
usually measured in micropascals ([mu]Pa), where 1 pascal (Pa) is the
pressure resulting from a force of one newton exerted over an area of
one square meter. Sound pressure level (SPL) is expressed as the ratio
of a measured sound pressure and a reference level. The commonly used
reference pressure level in underwater acoustics is 1 [mu]Pa, and the
units for SPLs are dB re 1 [mu]Pa. SPL (in decibels [dB]) = 20 log
(pressure/reference pressure).
SPL is an instantaneous measurement and can be expressed as the
peak, the peak-to-peak (p-p), or the root mean square (rms). Root mean
square, which is the square root of the arithmetic average of the
squared instantaneous pressure values, is typically used in discussions
of the effects of sounds on vertebrates and all references to SPL in
this document refer to the root mean square unless otherwise noted. SPL
does not take the duration of a sound into account.
Characteristics of the Airgun Pulses
Airguns function by venting high-pressure air into the water, which
creates an air bubble. The pressure signature of an individual airgun
consists of a sharp rise and then fall in pressure, followed 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 downward-directed source levels of the airgun arrays
used by SIO on the Revelle do not represent actual sound levels that
can be measured at any location in the water. Rather, they represent
the level that would be found 1 m (3.3 ft) from a hypothetical point
source emitting the same total amount of sound as is emitted by the
combined GI airguns. The actual received level at any location in the
water near the GI airguns would not exceed the source level of the
strongest individual source. In this case, that would be about 224.6 dB
re 1 [micro]Pam peak or 229.8 dB re 1 [micro]Pam peak-to-peak for the
two 45 in\3\ airgun array. However, the difference between rms and peak
or peak-to-peak values for a given pulse depends on the frequency
content and duration of the pulse, among other factors. Actual levels
experienced by any organism more than 1 m from either GI airgun would
be significantly lower.
Accordingly, L-DEO has predicted and modeled the received sound
levels in relation to distance and direction from the two GI airgun
array. These are the nominal source levels applicable to downward
propagation. A detailed description of L-DEO's modeling for this
survey's marine seismic source arrays for protected species mitigation
is provided in the ``Programmatic
[[Page 15065]]
Environmental Impact Statement/Overseas Environmental Impact Statement
prepared for Marine Seismic Research that is funded by the National
Science Foundation and conducted by the U.S. Geological Survey'' (NSF/
USGS PEIS, 2011). The NSF/USGS PEIS discusses the characteristics of
the airgun pulses. NMFS refers the reviewers to that document for
additional information.
Predicted Sound Levels for the Airguns
To estimate takes and determine mitigation (i.e., buffer and
exclusion) zones for the airgun array to be used, received sound levels
have been modeled by L-DEO for a number of airgun configurations,
including two 45 in\3\ G airguns, in relation to distance and direction
from the airguns (see Figure 2 of the IHA application). The model does
not allow for bottom interactions, and is most directly applicable to
deep water. Because the model results are for G airguns, which have
more energy than GI airguns of the same size, those distances
overestimate (by approximately 10%) the distances for the two 45 in\3\
GI airguns. Although the distances are overestimated, no adjustments
for this have been made to the radii distances in Table 2 (below).
Based on the modeling, estimates of the maximum distances from the GI
airguns where sound levels of 190, 180, and 160 dB re 1 [micro]Pa (rms)
are predicted to be received in intermediate and deep water are shown
in Table 2 (see Table 1 of the IHA application).
Empirical data concerning the 190, 180, and 160 dB (rms) distances
were acquired for various airgun arrays based on measurements during
the acoustic verification studies conducted by L-DEO in the northern
Gulf of Mexico (GOM) in 2003 (Tolstoy et al., 2004) and 2007 to 2008
(Tolstoy et al., 2009; Diebold et al., 2010). Results of the 18 and 36
airgun array are not relevant for the two GI airguns to be used in the
proposed low-energy seismic survey because the airgun arrays are not
the same size or volume. The empirical data for the 6, 10, 12, and 20
airgun arrays indicate that, for deep water, the L-DEO model tends to
overestimate the received sound levels at a given distance (Tolstoy et
al., 2004). For the two G airgun array, measurements were obtained only
in shallow water. When compared to measurements in acquired in deep
water, mitigation radii provided by the L-DEO model for the proposed
airgun operations were found to be conservative. The acoustic
verification surveys also showed that distances to given received
levels vary with water depth; these are larger in shallow water, while
intermediate/slope environments show characteristics intermediate
between those of shallow water and those of deep water environments,
and documented the influence of a sloping seafloor. The only
measurements obtained for intermediate depths during either survey were
for the 36-airgun array in 2007 to 2008 (Diebold et al., 2010).
Following results obtained at this site and earlier practice, a
correction factor of 1.5, irrespective of distance to the airgun array,
is used to derive intermediate-water radii from modeled deep-water
radii.
Measurements were not made for a two GI airgun array in
intermediate and deep water; however, SIO proposes to use the buffer
and exclusion zones predicted by L-DEO's model for the proposed GI
airgun operations in intermediate and deep water, although they are
likely conservative given the empirical results for the other arrays.
Using the L-DEO model, Table 2 (below) shows the distances at which
three rms sound levels are expected to be received from the two GI
airguns. The 160 dB re 1 [mu]Pam (rms) isopleth is the threshold
specified by NMFS for potential Level B (behavioral) harassment from
impulsive noise for both cetaceans and pinnipeds. The 180 and 190 dB re
1 [mu]Pam (rms) isopleths are the thresholds currently used to estimate
potential Level A harassment as specified by NMFS (2000) and are
applicable to cetaceans and pinnipeds, respectively. Table 2 summarizes
the predicted distances at which sound levels (160, 180, and 190 dB
[rms]) are expected to be received from the two airgun array (each 45
in\3\) operating in intermediate water (100 to 1,000 m [328.1 to 3,280
ft]) and deep water (>1,000 m) depths.
Table 2--Predicted and Modeled (Two 45 in\3\ GI Airgun Array) Distances to Which Sound Levels >=160, 180, and
190 dB re 1 [mu]Pa (rms) Could Be Received in Intermediate and Deep Water During the Proposed Low-Energy Seismic
Survey in the Southwest Pacific Ocean, East of New Zealand, May to June 2015
----------------------------------------------------------------------------------------------------------------
Predicted RMS radii distances (m) for 2 GI airgun
Tow depth array
Source and total volume (m) Water depth (m) ----------------------------------------------------
160 dB 180 dB 190 dB
----------------------------------------------------------------------------------------------------------------
Two 45 in\3\ GI Airguns (90 2 Intermediate 600 (1,968.5 ft) 100 (328.1 ft) 15 (49.2 ft)
in\3\). (100 to 1,000). *100 would be
used for
pinnipeds as
described in
NSF/USGS PEIS*
Two 45 in\3\ GI Airguns (90 2 Deep (>1,000).. 400 (1,312.3 ft) 100 (328.1 m) 10 (32.8 ft)
in\3\). *100 would be
used for
pinnipeds as
described in
NSF/USGS PEIS*
----------------------------------------------------------------------------------------------------------------
Based on the NSF/USGS PEIS and Record of Decision, for situations
which incidental take of marine mammals is anticipated, proposed
exclusion zones of 100 m for cetaceans and pinnipeds for all low-energy
acoustic sources in water depths greater than 100 m would be
implemented.
NMFS expects that acoustic stimuli resulting from the proposed
operation of the two GI airgun array has the potential to harass marine
mammals. NMFS does not expect that the movement of the Revelle, during
the conduct of the low-energy seismic survey, has the potential to
harass marine mammals because the relatively slow operation speed of
the vessel (approximately 5 kts; 9.3 km/hr; 5.8 mph) during seismic
data acquisition should allow marine mammals to avoid the vessel.
Bathymetric Survey
Along with the low-energy airgun operations, two additional
geophysical (detailed swath bathymetry) measurements focused on a
specific study area within the Southwest Pacific Ocean would be made
using hull-mounted sonar system instruments from the Revelle for
operational and navigational purposes. The ocean floor would be mapped
with the Kongsberg EM 122 multi-beam echosounder and a Knudsen Chirp
3260 sub-bottom profiler. During bathymetric survey operations, when
the vessel is not towing seismic equipment, its average speed would be
approximately 10.1 kts (18.8 km/hr). In cases where higher resolution
bathymetric data is sought, the average speed may be as low as 5 kts
(9.3 km/hr). These sound sources would be operated continuously from
the Revelle throughout the cruise. Operating
[[Page 15066]]
characteristics for the instruments to be used are described below.
Multi-Beam Echosounder (Kongsberg EM 122)--The hull-mounted multi-
beam sonar would be operated continuously during the cruise to map the
ocean floor. This instrument would operate at a frequency of 10.5 to 13
(usually 12) kilohertz (kHz) and would be hull-mounted. The
transmitting beamwidth would be 1 or 2[deg] fore to aft and 150[deg]
athwartship (cross-track). The estimated maximum source energy level
would be 242 dB re 1[mu]Pa (rms). Each `ping' of eight (in water
greater than 1,000 m or four (in water less than 1,000 m) successive
fan-shaped transmissions, each ensonifying a sector that extends 1[deg]
fore to aft. Continuous-wave signals increase from 2 to 15 milliseconds
(ms) in water depths up to 2,600 m (8,530 ft), and FM chirp signals up
to 100 ms long would be used in water greater than 2,600 m. The
successive transmission span an overall cross-track angular extent of
about 150[deg], with 2 ms gaps between the pings for successive
sectors.
Sub-Bottom Profiler--The Revelle would operate a Knudsen 3260 sub-
bottom profiler continuously throughout the cruise simultaneously to
map and provide information about the seafloor sedimentary features and
bottom topography that is mapped simultaneously with the multi-beam
echosounder. The beam of the sub-bottom profiler would be transmitted
as a 27[deg] cone, directed downward by a 3.5 kHz transducer in the
hull of the Revelle. The nominal power output would be 10 kilowatt
(kW), but the actual maximum radiated power would be 3 kW or 222 dB
(rms). The ping duration would be up to 64 ms, and the ping interval
would be 1 second. A common mode of operation is a broadcast five
pulses at 1 second intervals followed by a 5 second pause. The sub-
bottom profiler would be capable of reaching depths of 10,000 m
(32,808.4 ft).
Acoustic Locator (Pinger)--A pinger would be deployed with certain
instruments and equipment (e.g., heat-flow probe) so these devices can
be located in the event they become detached from their lines. The
pinger used in the heat-flow measurement activities would be the
Datasonics model BFP-312HP. A pinger typically operates at a frequency
of 32.8 kHz, generates a 5 ms pulse per second (10 pulses over a 10
second period), and has an acoustical output of 210 dB re 1 [mu]Pa
(rms). The pinger would be used during heat-flow measurement operations
only. It would operate continuously during each heat-flow probe
deployment. Each heat-flow probe measurement would last approximately
24 hours.
Heat-Flow Probe Deployment
Heat-flow measurements would be made using a ``violin-bow'' probe
with 11 thermistors that provides real time (analog) telemetry of the
thermal gradient and in-situ thermal conductivity. The heat-flow probe
that would be used on the Revelle consists of a lance 6 centimeter (cm)
(2.4 in) in diameter and 3.5 m (11.5 ft) long, a sensor tube housing
thermistors and heater wires, and a 560 kg (1,234.6 lb) weight stand.
The probe would be lowered to the bottom, and a 12 kHz pinger attached
to the wire approximately 50 m (164 ft) above the instrument would
monitor the distance between the probe and bottom. The probe would be
driven into the sediment by gravity, and temperatures within the
sediment would be measured with equally spaced thermistors. On
completion of a measurement, the instrument would be hoisted 100 to 500
m (328.1 to 1,640.4 ft) above the sediment, the ship is maneuvered to a
new position, and the process is repeated. Heat-flow measurements can
generally be made at a rate of 1 to 2 hours per measurement,
approximately 15 minutes for the actual measurement and 45 to 90
minutes to reposition the ship and probe. Internal power allows 20 to
24 measurements during a single lowering of the tool, with profiles
lasting as long as 48 hours. Proposed heat-flow measurements would have
a nominal spacing of 0.5 to 1 km (0.3 to 0.5 nmi), which would be
decreased in areas of significant basement relief or of large changes
in gradient. Heat flow transect locations are shown in Figure 1 of the
IHA application, and details of the probe and its deployment are given
in Section (f) of the IHA application. In total, approximately 200
heat-flow measurements would be made.
Description of the Marine Mammals in the Specified Geographic Area of
the Proposed Specified Activity
Few scientific systematic surveys for marine mammals have been
conducted in the waters of New Zealand, and these mainly consist of
single-species surveys in shallow coastal waters (e.g., Dawson et al.,
2004; Slooten et al., 2004, 2006). Large-scale, multi-species marine
mammal surveys are lacking. Various sources for data on sightings in
the proposed study area were used to describe the occurrence of marine
mammals in the waters of New Zealand, such as opportunistic sighting
records presented in previous reports (including the New Zealand
Department of Conservation marine mammals sighting database) considered
in evaluating potential marine mammals in the proposed action area.
New Zealand is considered a ``hotspot'' for marine mammal species
richness (Kaschner et al., 2011). The marine mammals that generally
occur in the proposed action area belong to three taxonomic groups:
Mysticetes (baleen whales), odontocetes (toothed whales), and pinnipeds
(seals and sea lions). The marine mammal species that could potentially
occur within the Southwest Pacific Ocean in proximity to the proposed
action area East of New Zealand include 30 species of cetaceans (21
odontocetes and 9 mysticetes) and 2 species of pinnipeds (32 total
species of marine mammals).
Marine mammal species likely to be encountered in the proposed
study area that are listed as endangered under the U.S. Endangered
Species Act of 1973 (ESA; 16 U.S.C. 1531 et seq.), includes the
southern right (Eubalaena australis), humpback (Megaptera
novaeangliae), sei (Balaenoptera borealis), fin (Balaenoptera
physalus), blue (Balaenoptera musculus), and sperm (Physeter
macrocephalus) whale. The Maui's dolphin (Cephalorhynchus hectori maui)
and New Zealand sea lion (Phocartos hookeri) are two other species are
ranked as ``nationally critical'' in New Zealand (Baker et al., 2010).
Maui's dolphin is only found along the west coast of the North Island.
The northern range of the New Zealand sea lion is not expected to
extend to the proposed study area based on New Zealand's National
Aquatic Biodiversity Information System (NABIS, 2014) and is not
considered further.
In addition to the marine mammal species known to occur in the
Southwest Pacific Ocean off the east coast of New Zealand, there are 18
species of marine mammals (12 cetacean and 6 pinniped species) with
ranges that are known to potentially occur in the waters of the
proposed study area, but they are categorized as ``vagrant'' under the
New Zealand Threat Classification System (Baker et al., 2010). These
include: Dwarf sperm whale (Kogia sima), Arnoux's beaked whale
(Berardius arnouxi), ginkgo-toothed beaked whale (Mesoplodon
ginkgodens), pygmy beaked whale (Mesoplodon peruvianis), Type B, C, and
D killer whale (Orcinus orca), melon-headed whale (Peponocephala
electra), Risso's dolphin (Grampus griseus), Fraser's dolphin
(Lagenodelphis hosei), pantropical spotted dolphin (Stenella
attenuata), striped dolphin (Stenella coeruleoalba), rough-toothed
dolphin (Steno bredanensis), spectacled
[[Page 15067]]
porpoise (Phocoena dioptrica), Antarctic fur seal (Arctocephalus
gazelle), Subantarctic fur seal (Arctocephalus tropicalis), crabeater
seal (Lobodon carcinophagus), leopard seal (Hydrurga leptonyx), Ross
seal (Ommatophoca rossi), and Weddell seal (Leptonychotes weddellii).
According to Jefferson et al. (2008), the distributional range of
Hubb's beaked whale (Mesoplodon carlhubbsi) and True's beaked whale
(Mesoplodon mirus) may also include New Zealand waters. There are no
records of Hubb's beaked whale in New Zealand, and only a single record
of True's beaked whale, which stranded on the west coast of South
Island in November 2011 (Constantine et al., 2014). The spinner
dolphin's (Stenella longirostris) range includes tropical and
subtropical zones 40[deg] North to 40[deg] South, but would be
considered vagrant as well. However, these species are not expected to
occur where the proposed activities would take place. These species are
not considered further in this document. Table 3 (below) presents
information on the habitat, occurrence, distribution, abundance,
population, and conservation status of the species of marine mammals
that may occur in the proposed study area during May to June 2015.
Table 3--The Habitat, Occurrence, Range, Regional Abundance, and Conservation Status of Marine Mammals That May Occur in or Near the Proposed Low-Energy
Seismic Survey Area in the Southwest Pacific Ocean, East of New Zealand
[See text and tables 2 in SIO's IHA application for further details]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Species Habitat Occurrence Range Population estimate ESA 1 MMPA 2
--------------------------------------------------------------------------------------------------------------------------------------------------------
Mysticetes
--------------------------------------------------------------------------------------------------------------------------------------------------------
Southern right whale (Eubalaena Coastal, shelf, Common................. Circumpolar 20 to 8,000 \3\ to 15,000 EN D
australis). pelagic. 55[deg] South. \4\--Worldwide 12,000
\12\--Southern
Hemisphere 2,700
\12\--Sub-Antarctic
New Zealand.
Pygmy right whale (Caperea Pelagic and coastal... Rare................... Circumpolar 30 to NA.................... NL NC
marginata). 55[deg] South.
Humpback whale (Megaptera Pelagic, nearshore Common................. Cosmopolitan Migratory 35,000 to 42,000 3 12-- EN D
novaeangliae). waters, and banks. Southern Hemisphere.
Minke whale (Balaenoptera Pelagic and coastal... Uncommon............... Circumpolar--Southern 720,0000 to 750,000 12 NL NC
acutorostrata including dwarf sub- Hemisphere to 65[deg] 14 15--Southern
species). South. Hemisphere.
Antarctic minke whale (Balaenoptera Pelagic, ice floes, Uncommon............... 7[deg] South to ice 720,000 to 750,000 12 NL NC
bonaerensis). coastal. edge (usually 20 to 14 15--Southern
65[deg] South). Hemisphere.
Bryde's whale (Balaenoptera edeni). Pelagic and coastal... Rare................... Circumglobal--Tropical At least 30,000 to NL NC
and Subtropical Zones. 40,000 \3\--Worldwide
21,000 \12\--
Northwestern Pacific
Ocean 48,109 \13\.
Sei whale (Balaenoptera borealis).. Primarily offshore, Uncommon............... Migratory, Feeding 80,000 \3\--Worldwide EN D
pelagic. Concentration 40 to 10,000 \14\--South of
50[deg] South. Antarctic Convergence.
Fin whale (Balaenoptera physalus).. Continental slope, Uncommon............... Cosmopolitan, 140,000 \3\--Worldwide EN D
pelagic. Migratory. 15,000 \14\--South of
Antarctic Convergence.
Blue whale (Balaenoptera musculus; Pelagic, shelf, Uncommon............... Migratory Pygmy blue 8,000 to 9,000 \3\-- EN D
including pygmy blue whale coastal. whale--North of Worldwide 2,300 \12\--
[Balaenoptera musculus Antarctic Convergence True Southern
brevicauda]). 55[deg] South. Hemisphere 1,500
\14\--Pygmy.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Odontocetes
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sperm whale (Physeter Pelagic, deep sea..... Common................. Cosmopolitan, 360,000 \3\--Worldwide EN D
macrocephalus). Migratory. 30,000 \13\--South of
Antarctic Convergence.
Dwarf sperm whale (Kogia sima)..... Shelf, Pelagic........ Vagrant................ Circumglobal--Tropical NA.................... NL NC
and Temperate Zones.
Pygmy sperm whale (Kogia breviceps) Shelf, Pelagic........ Uncommon............... Circumglobal--Temperat NA.................... NL NC
e Zones.
Arnoux's beaked whale (Berardius Pelagic............... Vagrant................ Circumpolar in NA.................... NL NC
arnuxii). Southern Hemisphere,
24 to 78[deg] South.
Cuvier's beaked whale (Ziphius Pelagic............... Uncommon............... Cosmopolitan.......... 600,000 14 16......... NL NC
cavirostris).
Southern bottlenose whale Pelagic............... Rare................... Circumpolar--30[deg] 500,000 \3\--South of NL NC
(Hyperoodon planifrons). South to ice edge. Antarctic Convergence
600,000 14 16.
Shepherd's beaked whale (Tasmacetus Pelagic............... Rare................... Circumpolar--Cold 600,000 14 16......... NL NC
shepherdi). temperate waters
Southern Hemisphere.
[[Page 15068]]
Andrew's beaked whale (Mesoplodon Pelagic............... Rare................... Circumpolar--temperate 600,000 14 16......... NL NC
bowdoini). waters of Southern
Hemisphere, 32 to
55[deg] South.
Blainville's beaked whale Pelagic............... Rare................... Circumglobal--tropical 600,000 14 16......... NL NC
(Mesoplodon densirostris). and temperate waters.
Ginkgo-toothed beaked whale Pelagic............... Vagrant................ Tropical and Temperate NA.................... NL NC
(Mesoplodon ginkgodens). waters--Indo-Pacific
Ocean.
Gray's beaked whale (Mesoplodon Pelagic............... Common................. 30[deg] South to 600,000 14 16......... NL NC
grayi). Antarctic waters.
Hector's beaked whale (Mesoplodon Pelagic............... Rare................... Circumpolar--cool 600,000 14 16......... NL NC
hectori). temperate waters of
Southern Hemisphere.
Hubb's beaked whale (Mesoplodon Pelagic............... Vagrant................ North Pacific Ocean... NA.................... NL NC
carlhubbsi).
Pygmy beaked whale (Mesoplodon Pelagic............... Vagrant................ 28[deg] North to NA.................... NL NC
peruvianis). 30[deg] South in
Pacific Ocean.
Spade-toothed beaked whale Pelagic............... Rare................... Circumantarctic....... 600,000 14 16......... NL NC
(Mesoplodon traversii).
Strap-toothed beaked whale Pelagic............... Uncommon............... 30[deg] South to 600,000 14 16......... NL NC
(Mesoplodon layardii). Antarctic Convergence.
True's beaked whale (Mesoplodon Pelagic............... Vagrant................ Anti-tropical in NA.................... NL NC
mirus). Northern and Southern
Hemisphere.
Killer whale (Orcinus orca)........ Pelagic, shelf, Common................. Cosmopolitan.......... 80,000 \3\--South of NL NC
coastal, pack ice. Antarctic Convergence.
False killer whale (Pseudorca Pelagic, shelf, Uncommon............... Circumglobal--tropical NA.................... NL NC
crassidens). coastal. and warmer temperate
water.
Long-finned pilot whale Pelagic, shelf, Common................. Circumpolar--19 to 200,000 3 5 14--South NL NC
(Globicephala melas). coastal. 68[deg] South in of Antarctic
Southern Hemisphere. Convergence.
Short-finned pilot whale Pelagic, shelf, Uncommon............... Circumglobal--50[deg] At least 600,000 \3\-- NL NC
(Globicephala macrocephalus). coastal. North to 40[deg] Worldwide.
South.
Melon-headed whale (Peponocephala Pelagic, shelf, Vagrant................ Circumglocal--40[deg] 45,000 \3\--Eastern NL NC
electra). coastal. North to 35[deg] Tropical Pacific
South. Ocean.
Bottlenose dolphin (Tursiops Coastal, shelf, Common................. 45[deg] North to At least 614,000 \3\-- NL, *C NC
truncatus). offshore. 45[deg] South. Worldwide.
Dusky dolphin (Lagenorhynchus Shelf, slope.......... Common................. Temperate waters-- 12,000 to 20,000 \17\-- NL NC
obscurus). Southern Hemisphere. New Zealand.
Fraser's dolphin (Lagenodelphis Pelagic............... Vagrant................ Pantropical--30[deg] 289,000 \3\--Eastern NL NC
hosei). North to 30[deg] Tropical Pacific
South. Ocean.
Hector's dolphin (Cephalorhynchus Nearshore............. Rare................... Shallow coastal 7,400 \17\............ C NC
hectori; including Maui's dolphin waters--New Zealand
subspecies [C. h. maui]). (Maui's dolpin--west
North Island).
Hourglass dolphin (Lagenorhynchus Pelagic, ice edge..... Uncommon............... 33[deg] South to pack 144,000 \3\ to 150,000 NL NC
cruciger). ice. \14\--South of
Antarctic Convergence.
Pantropical spotted dolphin Coastal, shelf, slope. Vagrant................ Circumglobal--40[deg] At least 2,000,000 NL NC
(Stenella attenuata). North to 40[deg] \3\--Worldwide.
South.
Spinner dolphin (Stenella Mainly nearshore...... Vagrant................ Circumglobal--40[deg] At least 1,200,000 NL NC
longirostris). North to 40[deg] \3\--Worldwide.
South.
Striped dolphin (Stenella Off continental shelf, Vagrant................ Circumglobal--50 to 40 At least 1,100,000 NL NC
coeruleoalba). convergence zones, South. \3\--Worldwide.
upwelling.
Risso's dolphin (Grampus griseus).. Slope, Pelagic........ Vagrant................ Circumglobal--Tropical At least 330,000 \3\-- NL NC
and Temperate waters. Worldwide.
Rough-toothed dolphin (Steno Pelagic............... Vagrant................ Circumglobal--40[deg] NA.................... NL NC
bredanensis). North to 35[deg]
South.
[[Page 15069]]
Short-beaked common dolphin Pelagic............... Common................. Circumglobal--tropical At least 3,500,000 NL NC
(Delphinus delphis). and warm temperate \3\--Worldwide.
waters.
Southern right whale dolphin Pelagic............... Uncommon............... 12 to 65[deg] South... NA.................... NL NC
(Lissodelphis peronii).
Spectacled porpoise (Phocoena Coastal, pelagic...... Vagrant................ Circumpolar--Southern NA.................... NL NC
dioptrica). Hemisphere.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Pinnipeds
--------------------------------------------------------------------------------------------------------------------------------------------------------
Crabeater seal (Lobodon Coastal, pack ice..... Vagrant................ Circumpolar--Antarctic 5,000,000 to NL NC
carcinophaga). 15,000,000 3 6--
Worldwide.
Leopard seal (Hydrurga leptonyx)... Pack ice, sub- Vagrant................ Sub-Antarctic islands 220,000 to 440,000 3 NL NC
Antarctic islands. to pack ice. 7--Worldwide.
Ross seal (Ommatophoca rossii)..... Pack ice, smooth ice Vagrant................ Circumpolar--Antarctic 130,000 \3\ 20,000 to NL NC
floes, pelagic. 220,000 \11\--
Worldwide.
Weddell seal (Leptonychotes Fast ice, pack ice, Vagrant................ Circumpolar--Southern 500,000 to 1,000,000 3 NL NC
weddellii). sub-Antarctic islands. Hemisphere. 8--Worldwide.
Southern elephant seal (Mirounga Coastal, pelagic, sub- Uncommon............... Circumpolar--Antarctic 640,000 \9\ to 650,000 NL NC
leonina). Antarctic waters. Convergence to pack \3\--Worldwide
ice. 470,000--South
Georgia Island \11\
607,000 \17\.
Antarctic fur seal (Arctocephalus Shelf, rocky habitats. Vagrant................ Sub-Antarctic islands 1,600,000 \10\ to NL NC
gazella). to pack ice edge. 3,000,000 \3\--
Worldwide.
New Zealand fur seal (Arctocephalus Rocky habitats, sub- Common................. North and South 135,000 \3\--Worldwide NL NC
forsteri). Antarctic islands. Islands, New Zealand 50,000 to 100,000
Southern and Western \18\--New Zealand.
Australia.
Subantarctic fur seal Shelf, rocky habitats. Vagrant................ Subtropical front to Greater than 310,000 NL NC
(Arctocephalus tropicalis). sub-Antarctic islands \3\--Worldwide.
and Antarctica.
New Zealand sea lion (Phocarctos Shelf, rocky habitats. Rare................... Sub-Antarctic islands 12,500 \3\............ NL NC
hookeri). south of New Zealand.
--------------------------------------------------------------------------------------------------------------------------------------------------------
NA = Not available or not assessed.
* Fjordland population.
\1\ U.S. Endangered Species Act: EN = Endangered, T = Threatened, DL = Delisted, NL = Not listed, C = Candidate.
\2\ U.S. Marine Mammal Protection Act: D = Depleted, S = Strategic, NC = Not Classified.
\3\ Jefferson et al., 2008.
\4\ Kenney, 2009.
\5\ Olson, 2009.
\6\ Bengston, 2009.
\7\ Rogers, 2009.
\8\ Thomas and Terhune, 2009.
\9\ Hindell and Perrin, 2009.
\10\ Arnould, 2009.
\11\ Academic Press, 2009.
\12\ IWC, 2014.
\13\ IWC, 1981.
\14\ Boyd, 2002.
\15\ Dwarf and Antarctic minke whale combined.
\16\ All Antarctic beaked whales combined.
\17\ New Zealand Department of Conservation.
\18\ Suisted and Neale, 2004.
Refer to sections 3 and 4 of SIO's IHA application for detailed
information regarding the abundance and distribution, population
status, and life history and behavior of these marine mammal species
and their occurrence in the proposed action area. The IHA application
also presents how SIO calculated the estimated densities for the marine
mammals in the proposed study area. NMFS has reviewed these data and
determined them to be the best available scientific information for the
purposes of the proposed IHA.
Potential Effects of the Proposed Specified Activity on Marine Mammals
This section includes a summary and discussion of the ways that the
types of stressors associated with the specified activity (e.g.,
seismic airgun operation, vessel movement, and gear deployment) have
been thought to impact marine mammals. This discussion may also include
reactions that we consider to rise to the level of a take and those
that we do not consider to rise to the level of take (for example, with
acoustics, we may include a discussion of studies that showed animals
not reacting at all to sound or exhibiting barely measureable
avoidance). This section is intended as a background of potential
effects and
[[Page 15070]]
does not consider either the specific manner in which this activity
would be carried out or the mitigation that would be implemented, and
how either of those would shape the anticipated impacts from this
specific activity. The ``Estimated Take by Incidental Harassment''
section later in this document would include a quantitative analysis of
the number of individuals that are expected to be taken by this
activity. The ``Negligible Impact Analysis'' section will include the
analysis of how this specific activity will impact marine mammals and
will consider the content of this section, the ``Estimated Take by
Incidental Harassment'' section, the ``Proposed Mitigation'' section,
and the ``Anticipated Effects on Marine Mammal Habitat'' section to
draw conclusions regarding the likely impacts of this activity on the
reproductive success or survivorship of individuals and from that on
the affected marine mammal populations or stocks.
When considering the influence of various kinds of sound on the
marine environment, it is necessary to understand that different kinds
of marine life are sensitive to different frequencies of sound. Based
on available behavioral data, audiograms have been derived using
auditory evoked potentials, anatomical modeling, and other data,
Southall et al. (2007) designate ``functional hearing groups'' for
marine mammals and estimate the lower and upper frequencies of
functional hearing of the groups. The functional groups and the
associated frequencies are indicated below (though animals are less
sensitive to sounds at the outer edge of their functional range and
most sensitive to sounds of frequencies within a smaller range
somewhere in the middle of their functional hearing range):
Low-frequency cetaceans (13 species of mysticetes):
Functional hearing is estimated to occur between approximately 7 Hz and
30 kHz;
Mid-frequency cetaceans (32 species of dolphins, six
species of larger toothed whales, and 19 species of beaked and
bottlenose whales): Functional hearing is estimated to occur between
approximately 150 Hz and 160 kHz;
High-frequency cetaceans (eight species of true porpoises,
six species of river dolphins, Kogia spp., the franciscana [Pontoporia
blainvillei], and four species of cephalorhynchids): Functional hearing
is estimated to occur between approximately 200 Hz and 180 kHz; and
Phocid pinnipeds in water: Functional hearing is estimated
to occur between approximately 75 Hz and 100 kHz;
Otariid pinnipeds in water: Functional hearing is
estimated to occur between approximately 100 Hz and 40 kHz.
As mentioned previously in this document, 32 marine mammal species
(30 cetacean and 2 pinniped species) are likely to occur in the
proposed low-energy seismic survey area. Of the 30 cetacean species
likely to occur in SIO's proposed action area, 9 are classified as low-
frequency cetaceans (southern right, pygmy right, humpback, minke,
Antarctic minke, Bryde's, sei, fin, and blue whale), 20 are classified
as mid-frequency cetaceans (sperm, Cuvier's beaked, Shepherd's beaked,
southern bottlenose, Andrew's beaked, Blainville's beaked, Gray's
beaked, Hector's beaked, spade-toothed beaked, strap-toothed beaked,
killer, false killer, long-finned pilot, and short-finned pilot whale,
and bottlenose, dusky, Hector's, hourglass, short-beaked common, and
southern right whale dolphin), and 1 is classified as high-frequency
cetaceans (pygmy sperm whale) (Southall et al., 2007). Of the 2
pinniped species likely to occur in SIO's proposed action area, 1 is
classified as phocid (southern elephant seal) and 1 is classified as
otariid (New Zealand fur seal) (Southall et al., 2007). A species
functional hearing group is a consideration when we analyze the effects
of exposure to sound on marine mammals.
Acoustic stimuli generated by the operation of the airguns, which
introduce sound into the marine environment, have the potential to
cause Level B harassment of marine mammals in the proposed study 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 hearing impairment, or non-auditory
physical or physiological effects (Richardson et al., 1995; Gordon et
al., 2004; Nowacek et al., 2007; Southall et al., 2007). Permanent
hearing impairment, in the unlikely event that it occurred, would
constitute injury, but temporary threshold shift (TTS) is not an injury
(Southall et al., 2007; Le Prell, 2012). Although the possibility
cannot be entirely excluded, it is unlikely that the proposed project
would result in any cases of temporary or permanent hearing impairment,
or any significant non-auditory physical or physiological effects.
Based on the available data and studies described here, some behavioral
disturbance is expected. A more comprehensive review of these issues
can be found in the NSF/USGS PEIS (2011) and L-DEO's ``Final
Environmental Assessment of a Marine Geophysical Survey by the R/V
Marcus G. Langseth in the Atlantic Ocean off Cape Hatteras, September
to October 2014.''
Tolerance
Richardson et al. (1995) defines tolerance as the occurrence of
marine mammals in areas where they are exposed to human activities or
man-made 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
(Nieukirk et al., 2012). 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. 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).
The airguns for the proposed low-energy seismic survey have
dominant frequency components of 0 to 188 Hz. This frequency range
fully overlaps the lower part of the frequency range of odontocete
calls and/or functional hearing (full range about 150 Hz to 180 kHz).
Airguns also produce a small portion of their sound at mid and high
[[Page 15071]]
frequencies that overlap most, if not all, frequencies produced by
odontocetes. While it is assumed that mysticetes can detect acoustic
impulses from airguns and vessel sounds (Richardson et al., 1995a),
sub-bottom profilers, and most of the multi-beam echosounders would
likely be detectable by some mysticetes based on presumed mysticete
hearing sensitivity. Odontocetes are presumably more sensitive to mid
to high frequencies produced by the multi-beam echosounders and sub-
bottom profilers than to the dominant low frequencies produced by the
airguns and vessel. A more comprehensive review of the relevant
background information for odontocetes appears in Section 3.6.4.3,
Section 3.7.4.3 and Appendix E of the NSF/USGS PEIS (2011).
Masking effects of pulsed sounds (even from large arrays of
airguns) on marine mammal calls and other natural sounds are expected
to be limited. 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. Situations with prolonged strong reverberation are infrequent.
However, it is common for reverberation to cause some lesser degree of
elevation of the background level between airgun pulses (Gedamke, 2011;
Guerra et al., 2011, 2013), and this weaker reverberation presumably
reduces the detection range of calls and other natural sound to some
degree. Guerra et al. (2013) reported that ambient noise levels between
seismic pulses were elevated because of reverberation at ranges of 50
km (27 nmi) from the seismic source. Based on measurements in deep
water of the Southern Ocean, Gedamke (2011) estimated that the slight
elevation of background levels during intervals between pulses reduced
blue and fin whale communication space by as much as 36 to 51% when a
seismic survey was operating 450 to 2,800 km (243 to 1,511.9 nmi) away.
Based on preliminary modeling, Wittekind et al. (2013) reported that
airgun sounds could reduce the communication range of blue and fin
whales 2,000 km (1,079.9 nmi) from the seismic source. Klinck et al.
(2012) also found reverberation effects between pulses. Nieukirk et al.
(2012) and Blackwell et al. (2013) noted the potential for masking
effects from seismic surveys on large whales.
Some baleen and toothed whales are known to continue calling in the
presence of seismic pulses, and their calls can usually be heard
between the seismic pulses (e.g., Richardson et al., 1986; McDonald et
al., 1995; Greene et al., 1999; Nieukirk et al., 2004, 2012; 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 North
Atlantic Ocean went silent for an extended period starting soon after
the onset of a seismic survey in the area. Similarly, there has been
one report that sperm whales ceased calling when exposed to pulses from
a very distant seismic ship (Bowles et al., 1994). However, more recent
studies found that they continued calling in the presence of seismic
pulses (Madsen et al., 2002; Tyack et al., 2003; Smultea et al., 2004;
Holst et al., 2006; and Jochens et al., 2008). Cerchio et al. (2014)
suggested that the breeding display of humpback whales off Angola could
have been disrupted by seismic sounds, as singing activity declined
with increasing received levels. In addition, some cetaceans are known
to change their calling rates, shift their peak frequencies, or
otherwise modify their vocal behavior in response to airgun sounds (Di
Iorio and Clark, 2010; Castellote et al., 2012; Blackwell et al.,
2013). Di Iorio and Clark (2009) found evidence of increased calling by
blue whales during operations by a lower-energy seismic source (i.e.,
sparker). The hearing systems of baleen whales are undoubtedly more
sensitive to low-frequency sounds than are the ears of small
odontocetes that have been studied directly (MacGillivary et al.,
2013). Dolphins and porpoises commonly are heard calling while airguns
are operating (e.g., Gordon et al., 2004; Smultea et al., 2004; Holst
et al., 2005a, b; and Potter et al., 2007). The sounds important to
small odontocetes are predominantly at much higher frequencies than are
the dominant components of airgun sounds, thus limiting the potential
for masking.
Pinnipeds have the most sensitive hearing and/or produce most of
their sounds in frequencies higher than the dominant components of
airgun sound, but there is some overlap in the frequencies of the
airgun pulses and the calls. However, the intermittent nature of airgun
pules presumably reduces 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 (Di Iorio and Clark, 2009).
The North Atlantic right whales (Eubalaena glacialis) 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, NMFS expects
the masking effects of seismic pulses to 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; Ellison et al., 2012).
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 (New et al., 2013).
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);
[[Page 15072]]
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 sound. In most cases, this approach
likely overestimates the numbers of marine mammals that would be
affected in some biologically-important manner.
Baleen Whales--Baleen whales generally tend to avoid operating
airguns, but avoidance radii are quite variable (reviewed in Richardson
et al., 1995; Gordon et al., 2004). 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. In the cases of migrating gray
(Eschrichtius robustus) and bowhead (Balaena mysticetus) whales, the
observed changes in behavior appeared to be of little or no biological
consequence to the animals (Richardson et al., 1995). They simply
avoided the sound source by displacing their migration route to varying
degrees, but within the natural boundaries of the migration corridors
(Malme et al., 1984; Malme and Miles, 1985; Richardson et al., 1995).
Studies of gray, bowhead, and humpback whales have shown that
seismic pulses with received levels of 160 to 170 dB re 1 [mu]Pa (rms)
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 4 to 15 km (2.2 to
8.1 nmi) 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 have
shown that some species of baleen whales, notably bowhead, gray, and
humpback whales, at times, show strong avoidance at received levels
lower than 160 to 170 dB re 1 [mu]Pa (rms).
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 airgun (20 in\3\) with
source level of 227 dB re 1 [mu]Pa (p-p). In the 1998 study, they
documented that avoidance reactions began at 5 to 8 km (2.7 to 4.3 nmi)
from the array, and that those reactions kept most pods approximately 3
to 4 km (1.6 to 2.2 nmi) from the operating seismic boat. In the 2000
study, they noted localized displacement during migration of 4 to 5 km
(2.2 to 2.7 nmi) by traveling pods and 7 to 12 km (3.8 to 6.5 nmi) by
more sensitive resting pods of cow-calf pairs. Avoidance distances with
respect to the single airgun were smaller but consistent with the
results from the full array in terms of the received sound levels. The
mean received level for initial avoidance of an approaching airgun was
140 dB re 1 [mu]Pa (rms) for humpback pods containing females, and at
the mean closest point of approach distance the received level was 143
dB re 1 [mu]Pa (rms). The initial avoidance response generally occurred
at distances of 5 to 8 km (2.7 to 4.3 nmi) from the airgun array and 2
km (1.1 nmi) from the single airgun. However, some individual humpback
whales, especially males, approached within distances of 100 to 400 m
(328 to 1,312 ft), where the maximum received level was 179 dB re 1
[mu]Pa (rms). Studies examining the behavioral responses of humpback
whales to airguns are currently underway off eastern Australia (Cato et
al., 2011, 2012, 2013).
Data collected by observers during several seismic surveys in the
Northwest Atlantic 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 vs. 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 dB re 1 [mu]Pa (rms). 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.
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). The evidence for this was
circumstantial and subject to alternative explanations (IAGC, 2004).
Also, the evidence was not consistent with subsequent results from the
same area of Brazil (Parente et al., 2006), or with direct studies of
humpbacks exposed to seismic surveys in other areas and seasons. After
allowance for data from subsequent years, there was ``no observable
direct correlation'' between strandings and seismic surveys (IWC, 2007:
236).
There are no reactions of right whales to seismic surveys. However,
Rolland et al. (2012) suggested that ship noise causes increased stress
in right whales; they showed that baseline levels of stress-related
fecal hormone metabolites decreased in North Atlantic right whales with
a 6 dB decrease in underwater noise from vessels. Wright et al. (2011)
also reported that sound could be a potential source of stress for
marine mammals.
Results from bowhead whales show that their responsiveness can be
quite variable depending on their activity (migrating versus feeding).
Bowhead whales migrating west across the Alaskan Beaufort Sea in
autumn, in particular, are unusually responsive, with substantial
avoidance occurring out to distances of 20 to 30 km (10.8 to 16.2 nmi)
from a medium-sized airgun source (Miller et al., 1999; Richardson et
al., 1999). However, more recent research on bowhead whales
corroborates earlier evidence that, during the summer feeding season,
bowheads are not as sensitive to seismic sources (Miller et al., 2005).
Nonetheless, Robertson et al. (2013) showed that bowheads on their
summer feeding grounds showed subtle but statistically significant
changes in surfacing-respiration-dive cycles during exposure to seismic
sounds, including
[[Page 15073]]
shorter surfacing intervals, shorter dives, and decreased number of
blows per surface interval.
Bowhead whale calls detected in the presence and absence of airgun
sounds have been studied extensively in the Beaufort Sea. Bowheads
continue to produce calls of the usual types when exposed to airgun
sounds on their summering grounds, although number of calls detected
are significantly lower in the presence than in the absence of airgun
pulses; Blackwell et al. (2013) reported that calling rates in 2007
declined significantly where received SPLs from airgun sounds were 116
to 129 dB re 1 [mu]Pa. Thus, bowhead whales in the Beaufort Sea
apparently decrease their calling rates in response to seismic
operations, although movement out of the area could also contribute to
the lower call detection rate (Blackwell et al., 2013).
A multivariate analysis of factors affecting the distribution of
calling bowhead whales during their fall migration in 2009 noted that
the southern edge of the distribution of calling whales was
significantly closer to shore with increasing levels of airgun sound
from a seismic survey a few hundred kms to the east of the study area
(i.e., behind the westward-migrating whales; McDonald et al., 2010,
2011). It was not known whether this statistical effect represented a
stronger tendency for quieting of the whales farther offshore in deeper
water upon exposure to airgun sound, or an actual inshore displacement
of whales.
Reactions of migrating and feeding (but not wintering) gray whales
to seismic surveys have been studied. Malme et al. (1986, 1988) studied
the responses of feeding eastern Pacific gray whales to pulses from a
single 100 in\3\ airgun off St. Lawrence Island in the northern Bering
Sea. They estimated, based on small sample sizes, that 50 percent of
feeding gray whales stopped feeding at an average received pressure
level of 173 dB re 1 [mu]Pa on an (approximate) rms basis, and that 10
percent of feeding whales interrupted feeding at received levels of 163
dB re 1 [mu]Pa (rms). Those findings were generally consistent with the
results of experiments conducted on larger numbers of gray whales that
were migrating along the California coast (Malme et al., 1984; Malme
and Miles, 1985), and western Pacific gray whales feeding off Sakhalin
Island, Russia (Wursig et al., 1999; Gailey et al., 2007; Johnson et
al., 2007; Yazvenko et al., 2007a, b), along with data on gray whales
off British Columbia (Bain and Williams, 2006).
Various species of Balaenoptera (blue, sei, fin, and minke whales)
have occasionally been seen in areas ensonified by airgun pulses
(Stone, 2003; MacLean and Haley, 2004; Stone and Tasker, 2006), and
calls from blue and fin whales have been localized in areas with airgun
operations (e.g., McDonald et al., 1995; Dunn and Hernandez, 2009;
Castellote et al., 2010). Sightings by observers on seismic vessels off
the United Kingdom from 1997 to 2000 suggest that, during times of good
sightability, sighting rates for mysticetes (mainly fin and sei whales)
were similar when large arrays of airguns were shooting versus 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,
2012) reported that singing fin whales in the Mediterranean moved away
from an operating airgun array, and their song notes had low bandwidths
during periods with versus without airgun sounds.
Ship-based monitoring studies of baleen whales (including blue,
fin, sei, minke, and humpback whales) in the Northwest Atlantic found
that overall, this group had lower sighting rates during seismic vs.
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, 2010). The western
Pacific gray whale population did not seem affected by a seismic survey
in its feeding ground during a previous year (Johnson et al., 2007).
Similarly, bowhead whales have continued to travel to the eastern
Beaufort Sea each summer, and their numbers have increased notably,
despite seismic exploration in their summer and autumn range for many
years (Richardson et al., 1987; Allen and Angliss, 2010).
Toothed Whales--Little systematic information is available about
reactions of toothed whales to noise pulses. Few studies similar to the
more extensive baleen whale/seismic pulse work summarized above have
been reported for toothed whales. However, there are recent systematic
studies on sperm whales (e.g., Gordon et al., 2006; Madsen et al.,
2006; Winsor and Mate, 2006; Jochens et al., 2008; Miller et al.,
2009). There is an increasing amount of information about responses of
various odontocetes to seismic surveys based on monitoring studies
(e.g., Stone, 2003; Smultea et al., 2004; Moulton and Miller, 2005;
Bain and Williams, 2006; Holst et al., 2006; Stone and Tasker, 2006;
Potter et al., 2007; Hauser et al., 2008; Holst and Smultea, 2008;
Weir, 2008; Barkaszi et al., 2009; Richardson et al., 2009; Moulton and
Holst, 2010).
Seismic operators and PSOs on seismic vessels regularly see
dolphins and other small toothed whales near operating airgun arrays,
but in general there is a tendency for most delphinids to show some
avoidance of operating seismic vessels (e.g., Goold, 1996a,b,c;
Calambokidis and Osmek, 1998; Stone, 2003; Moulton and Miller, 2005;
Holst et al., 2006; Stone and Tasker, 2006; Weir, 2008; Richardson et
al., 2009; Barkaszi et al., 2009; Moulton and Holst, 2010; Barry et
al., 2012). 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
[[Page 15074]]
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.
Preliminary findings of a monitoring study of narwhals (Monodon
monoceros) in Melville Bay, Greenland (summer and fall 2012) showed no
short-term effects of seismic survey activity on narwhal distribution,
abundance, migration timing, and feeding habits (Heide-Jorgensen et
al., 2013a). In addition, there were no reported effects on narwhal
hunting. These findings do not seemingly support a suggestion by Heide-
Jorgensen et al. (2013b) that seismic surveys in Baffin Bay may have
delayed the migration timing of narwhals, thereby increasing the risk
of narwhals to ice entrapment.
Results of 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 (Phocoenoides
dalli) (Stone, 2003; MacLean and Koski, 2005; Bain and Williams, 2006;
Stone and Tasker, 2006). Thompson et al. (2013) reported decreased
densities and reduced acoustic detections of harbor porpoise in
response to a seismic survey in Moray Firth, Scotland, at ranges of 5
to 10 km (2.7 to 5.4 nmi) (SPLs of 165 to 172 dB re 1 [mu]Pa; sound
exposure levels (SELs) of 145 to 151 dB [mu]Pa\2\s); however, animals
returned to the area within a few hours. Dall's porpoises seem
relatively tolerant of airgun operations (MacLean and Koski, 2005; Bain
and Williams, 2006), although they too have been observed to avoid
large arrays of operating airguns (Calambokidis and Osmek, 1998; Bain
and Williams, 2006). This apparent difference in responsiveness of
these two porpoise species is consistent with their relative
responsiveness to boat traffic and some other acoustic sources
(Richardson et al., 1995; Southall et al., 2007).
Most studies of sperm whales exposed to airgun sounds indicate that
the sperm whale shows considerable tolerance of airgun pulses (e.g.,
Stone, 2003; Moulton et al., 2005, 2006a; Stone and Tasker, 2006; Weir,
2008). In most cases the whales do not show strong avoidance, and they
continue to call. 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 may be reduced by close approach
of vessels. In any event, it is likely that most beaked whales would
also show strong avoidance of an approaching seismic vessel, although
this has not been documented explicitly. In fact, Moulton and Holst
(2010) reported 15 sightings of beaked whales during seismic studies in
the Northwest Atlantic; seven of those sightings were made at times
when at least one airgun was operating. There was little evidence to
indicate that beaked whale behavior was affected by airgun operations;
sighting rates and distances were similar during seismic and non-
seismic periods (Moulton and Holst, 2010).
There are increasing indications that some beaked whales tend to
strand when naval exercises involving mid-frequency sonar operation are
ongoing nearby (e.g., Simmonds and Lopez-Jurado, 1991; Frantzis, 1998;
NOAA and USN, 2001; Jepson et al., 2003; Hildebrand, 2005; Barlow and
Gisiner, 2006; see also the ``Stranding and Mortality'' section in this
notice). These strandings are apparently a disturbance response,
although auditory or other injuries or other physiological effects may
also be involved. Whether beaked whales would ever react similarly to
seismic surveys is unknown. Seismic survey sounds are quite different
from those of the sonar in operation during the above-cited incidents.
Odontocete reactions to large arrays of airguns are variable and,
at least for delphinids, seem to be confined to a smaller radius than
has been observed for the more responsive of some 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).
Pinnipeds--Pinnipeds are not likely to show a strong avoidance
reaction to the airgun array. Visual monitoring from seismic vessels
has shown only slight (if any) avoidance of airguns by pinnipeds, and
only slight (if any) changes in behavior. In the Beaufort Sea, some
ringed seals avoided an area of 100 m to (at most) a few hundred meters
around seismic vessels, but many seals remained within 100 to 200 m
(328 to 656 ft) of the trackline as the operating airgun array passed
by (e.g., Harris et al., 2001; Moulton and Lawson, 2002; Miller et al.,
2005.). Ringed seal (Pusa hispida) sightings averaged somewhat farther
away from the seismic vessel when the airguns were operating than when
they were not, but the difference was small (Moulton and Lawson, 2002).
Similarly, in Puget Sound, sighting distances for harbor seals (Phoca
vitulina) and California sea lions (Zalophus californianus) tended to
be larger when airguns were operating (Calambokidis and Osmek, 1998).
Previous telemetry work suggests that avoidance and other behavioral
reactions by two other species of seals to small airgun sources may be
stronger than evident to date from visual studies of pinnipeds
reactions to airguns (Thompson et al., 1998).
During seismic exploration off Nova Scotia, gray seals (Halichoerus
grypus) exposed to noise from airguns and linear explosive charges did
not react strongly (J. Parsons in Greene et al., 1985). Pinnipeds in
both water and air, sometimes tolerate strong noise pulses from non-
explosive and explosive scaring devices, especially if attracted to the
area for feeding and reproduction (Mate and Harvey, 1987; Reeves et
al., 1996). Thus pinnipeds are expected to be rather tolerant of, or
habituate to, repeated underwater sounds from distant seismic sources,
at least when the animals are strongly attracted to the area.
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,
Carder, Schlundt, and Ridgway, 2005). Factors that influence the amount
of threshold shift include the amplitude, duration, frequency
[[Page 15075]]
content, temporal pattern, and energy distribution of noise exposure.
The magnitude of hearing threshold shift normally decreases over time
following cessation of the noise exposure. The amount of threshold
shift just after exposure is called the initial threshold shift. If the
threshold shift eventually returns to zero (i.e., the threshold returns
to the pre-exposure value), it is called temporary threshold shift
(TTS) (Southall et al., 2007). Researchers have studied TTS in certain
captive odontocetes and pinnipeds exposed to strong sounds (reviewed in
Southall et al., 2007). However, there has been no specific
documentation of TTS, let alone permanent hearing damage, i.e.,
permanent threshold shift (PTS), in free-ranging marine mammals exposed
to sequences of airgun pulses during realistic field conditions.
Temporary Threshold Shift--TTS is the mildest form of hearing
impairment that can occur during exposure to a strong sound (Kryter,
1985). While experiencing TTS, the hearing threshold rises and a sound
must be stronger in order to be heard. At least in terrestrial mammals,
TTS can last from minutes or hours to (in cases of strong TTS) days.
For sound exposures at or somewhat above the TTS threshold, hearing
sensitivity in both terrestrial and marine mammals recovers rapidly
after exposure to the noise ends. Few data on sound levels and
durations necessary to elicit mild TTS have been obtained for marine
mammals, and none of the published data concern TTS elicited by
exposure to multiple pulses of sound. Available data on TTS in marine
mammals are summarized in Southall et al. (2007). Table 2 (above)
presents the estimated distances from the Revelle's airguns at which
the received energy level (per pulse, flat-weighted) would be expected
to be greater than or equal to 180 and 190 dB re 1 [mu]Pa (rms).
The established 180 and 190 dB (rms) criteria are not considered to
be the levels above which TTS might occur. Rather, they are the
received levels above which, in the view of a panel of bioacoustics
specialists convened by NMFS before TTS 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. NMFS
also assumes that cetaceans and pinnipeds exposed to levels exceeding
160 dB re 1 [mu]Pa (rms) may experience Level B harassment.
For toothed whales, researchers have derived TTS 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 kPa (or 30 psi, peak-to-peak), which is equivalent to 228 dB re
1 Pa (peak-to-peak), resulted in a 7 and 6 dB TTS in the beluga whale
at 0.4 and 30 kHz, respectively. Thresholds returned to within 2 dB of
the pre-exposure level within 4 minutes of the exposure (Finneran et
al., 2002). For the one harbor porpoise tested, the received level of
airgun sound that elicited onset of TTS was lower (Lucke et al., 2009).
If these results from a single animal are representative, it is
inappropriate to assume that onset of TTS occurs at similar received
levels in all odontocetes (cf. Southall et al., 2007). Some cetaceans
apparently can incur TTS at considerably lower sound exposures than are
necessary to elicit TTS in the beluga or bottlenose dolphin.
For baleen whales, there are no data, direct or indirect, on levels
or properties of sound that are required to induce TTS. The frequencies
to which baleen whales are most sensitive are assumed to be lower than
those to which odontocetes are most sensitive, and natural background
noise levels at those low frequencies tend to be higher. As a result,
auditory thresholds of baleen whales within their frequency band of
best hearing are believed to be higher (less sensitive) than are those
of odontocetes at their best frequencies (Clark and Ellison, 2004).
From this, it is suspected that received levels causing TTS onset may
also be higher in baleen whales than those of odontocetes (Southall et
al., 2007).
In pinnipeds, researchers have not measured TTS 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 TTS at somewhat lower received levels than do small odontocetes
exposed for similar durations (Kastak et al., 1999, 2005; Ketten et
al., 2001). The TTS threshold for pulsed sounds has been indirectly
estimated as being an SEL of approximately 171 dB re 1
[mu]Pa\2\[middot]s (Southall et al., 2007) which would be equivalent to
a single pulse with a received level of approximately 181 to 186 dB re
1 [mu]Pa (rms), or a series of pulses for which the highest rms values
are a few dB lower. Corresponding values for California sea lions and
northern elephant seals (Mirounga angustirostris) are likely to be
higher (Kastak et al., 2005).
Additional data are needed to determine the received levels at
which small odontocetes would start to incur TTS upon exposure to
repeated, low-frequency pulses of airgun sounds with variable received
levels. To determine how close an airgun array would need to approach
in order to elicit TTS, one would (as a minimum) need to allow for the
sequence of distances at which airgun pulses would occur, and for the
dependence of received SEL on distance in the region of the airgun
operation (Breitzke and Bohlen, 2010; Laws, 2012). At the present state
of knowledge, it can be assumed that the effect is directly related to
total receive energy, although there is recent evidence that auditory
effects in a given animal are not a simple function of received
acoustic energy. Frequency, duration of the exposure and occurrence of
gaps within the exposure can also influence the auditory effect
(Finneran and Schlundt, 2010, 2011, 2013; Finneran et al., 2010a,b;
Finneran 2012; Ketten, 2012; Kastelein et al., 2013a).
The assumption that, in marine mammals, the occurrence and
magnitude of TTS is a function of cumulative acoustic energy (SEL) is
probably an oversimplification (Finneran, 2012). Popov et al. (2011)
examined the effects of fatiguing noise on the hearing threshold of
Yangtze finless porpoises (Neophocaena phocaenoides) when exposed to
frequencies of 32 to 128 kHz at 140 to 160 dB re 1 [mu]Pa for 1 to 30
minutes. They found that an exposure of higher level and shorter
duration produced a higher TTS than an exposure of equal SEL but of
lower level and longer duration. Kastelein et al. (2012a,b; 2013b) also
reported that the equal-energy model is not valid for predicting TTS in
harbor porpoises or harbor seals.
Recent data have shown that the SEL required for TTS onset to occur
increases with intermittent exposures, with some auditory recovery
during silent periods between (Finneran et al., 2010b; Finneran and
Schlundt, 2011). Schlundt et al. (2013) reported that the potential for
seismic surveys using airguns to cause auditory effects on dolphins
could be lower than previously thought. Based on behavioral tests,
Finneran et al. (2011) and Schlundt et al. (2013) reported no
measurable TTS in bottlenose dolphins after exposure to 10 impulses
from a seismic airgun with a cumulative SEL of approximately 195 dB re
1 [mu]Pa\2\s; results from auditory evoked potential measurements were
more variable (Schlundt et al., 2013).
Recent studies have also shown that the SEL necessary to elicit TTS
can depend substantially on frequency, with susceptibility to TTS
increasing with increasing frequency above 3 kHz (Finneran and
Schlundt, 2010, 2011; Finneran, 2012). When beluga whales
[[Page 15076]]
were exposed to fatiguing noise with sound levels of 165 dB re 1 [mu]Pa
for durations of 1 to 30 minutes at frequencies of 11.2 to 90 kHz, the
highest TTS with the longest recovery time was produced by lower
frequencies (11.2 and 22.5 kHz); TTS effects also gradually increased
with prolonged exposure time (Popov et al., 2013a). Popov et al.
(2013b) also reported that TTS produced by exposure to a fatiguing
noise was larger during the first session (or na[iuml]ve subject state)
with a beluga whale than TTS that resulted from the same sound in
subsequent sessions (experienced subject state). Therefore, Supin et
al. (2013) reported that SEL may not be a valid metric for examining
fatiguing sounds on beluga whales. Similarly, Nachtigall and Supin
(2013) reported that false killer whales are able to change their
hearing sensation levels when exposed to loud sounds, such as warning
signals or echolocation sounds.
It is inappropriate to assume that onset of TTS occurs at similar
received levels in all cetaceans (Southall et al., 2007). Some
cetaceans could incur TTS at lower sound exposures than are necessary
to elicit TTS in the beluga or bottlenose dolphin. Based on the best
available information, Southall et al. (2007) recommended a TTS
threshold for exposure to a single or multiple pulses of 183 dB re 1
[mu]Pa\2\s. Tougaard et al. (2013) proposed a TTS criterion of 165 dB
re 1 [mu]Pa\2\s for porpoises based on data from two recent studies.
Gedamke et al. (2011), based on preliminary simulation modeling that
attempted to allow for various uncertainties in assumptions and
variability around population means, suggested that some baleen whales
whose closest point of approach to a seismic vessel is 1 km or more
could experience TTS.
Permanent Threshold Shift--When PTS occurs, there is physical
damage to the sound receptors in the ear. In severe cases, there can be
total or partial deafness, whereas in other cases, the animal has an
impaired ability to hear sounds in specific frequency ranges (Kryter,
1985). There is no specific evidence that exposure to pulses of airgun
sound can cause PTS in any marine mammal, even with large arrays of
airguns. However, given the possibility that mammals close to an airgun
array might incur at least mild TTS, there has been further speculation
about the possibility that some individuals occurring very close to
airguns might incur PTS (e.g., Richardson et al., 1995, p. 372ff;
Gedamke et al., 2008). Single or occasional occurrences of mild TTS are
not indicative of permanent auditory damage, but repeated or (in some
cases) single exposures to a level well above that causing TTS onset
might elicit PTS.
Relationships between TTS and PTS thresholds have not been studied
in marine mammals but are assumed to be similar to those in humans and
other terrestrial mammals (Southall et al., 2007). PTS might occur at a
received sound level at least several dBs above that inducing mild TTS
if the animal were exposed to strong sound pulses with rapid rise
times. Based on data from terrestrial mammals, a precautionary
assumption is that the PTS threshold for impulse sounds (such as airgun
pulses as received close to the source) is at least 6 dB higher than
the TTS threshold on a peak-pressure basis, and probably greater than 6
dB (Southall et al., 2007). Given the higher level of sound necessary
to cause PTS as compared with TTS, it is considerably less likely that
PTS would occur. Baleen whales generally avoid the immediate area
around operating seismic vessels, as do some other marine mammals.
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,
some odontocetes, and some pinnipeds, are especially unlikely to incur
non-auditory physical effects.
There is no definitive evidence that any of these effects occur
even for marine mammals in close proximity to large airgun arrays.
However, Gray and Van Waerebeek (2011) have suggested a cause-effect
relationship between a seismic survey off Liberia in 2009 and the
erratic movement, postural instability, and akinesia in a pantropical
spotted dolphin based on spatially and temporally close association
with the airgun array. Additionally, 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
(Castellote and Llorens, 2013).
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
[[Page 15077]]
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--The proposed
action is not a military readiness activity or using military active
sonar (non-pulse). 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 (non-pulse sound) and, in one
case, the regional co-occurrence of an L-DEO seismic survey (Malakoff,
2002; Cox et al., 2006), has raised the possibility that beaked whales
exposed to strong ``pulsed'' sounds could also be 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 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. The evidence for this remains
circumstantial and associated with exposure to naval mid-frequency
sonar, not seismic surveys (Cox et al., 2006; Southall et al., 2007).
Seismic pulses and mid-frequency sonar signals are quite different,
and some mechanisms by which sonar sounds have been hypothesized to
affect beaked whales are unlikely to apply to airgun pulses. Sounds
produced by airgun arrays are broadband impulses with most of the
energy below one kHz. Typical military mid-frequency sonar emits non-
impulse sounds at frequencies of 2 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 expect that the same effects to marine mammals would
result from military sonar and seismic surveys. 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,
there was a stranding of two Cuvier's beaked whales in the Gulf of
California, Mexico, when the L-DEO vessel R/V Maurice Ewing was
operating a 20 airgun (8,490 in\3\) array in the general region. The
link between the stranding and the seismic surveys was inconclusive and
not based on any physical evidence (Hogarth, 2002; Yoder, 2002).
Nonetheless, the Gulf of California incident plus the beaked whale
strandings near naval exercises involving use of mid-frequency sonar
suggests a need for caution in conducting seismic surveys in areas
occupied by beaked whales until more is known about effects of seismic
surveys on those species (Hildebrand, 2005). No injuries of beaked
whales are anticipated during the proposed study because of:
(1) The high 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 to be used in the
proposed study and operated by SIO and those involved in the naval
exercises associated with strandings.
Potential Effects of Other Acoustic Devices and Sources
Multi-Beam Echosounder
SIO would operate the Kongsberg EM 122 multi-beam echosounder from
the source vessel during the planned study. Sounds from the multi-beam
echosounder are very short pulses, occurring for approximately 2 to 15
ms once every 5 to 20 seconds, depending on water depth. Most of the
energy in the sound pulses emitted by the multi-beam echosounder is at
frequencies near 12 kHz (10.5 to 13), and the maximum source level is
242 dB re 1 [mu]Pa (rms). 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 (in
water less than 1,000 m) consecutive successive fan-shaped
transmissions (segments) at different cross-track angles. Any given
marine mammal at depth near the trackline would be in the
[[Page 15078]]
main beam for only one or two of the eight 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 would receive only limited amounts of pulse energy because
of the short pulses. Animals close to the ship (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 a multi-beam 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 TTS.
Navy sonars that have been linked to avoidance reactions and
stranding of cetaceans: (1) Generally have longer pulse duration than
the Kongsberg EM 122; and (2) are often directed close to horizontally,
as well as omnidirectional, versus more downward and narrowly for the
multi-beam echosounder. The area of possible influence of the multi-
beam 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 SIO's operations, the individual
pulses would be very short, and a given mammal would not receive many
of the downward-directed pulses as the vessel passes by. Possible
effects of a multi-beam echosounder on marine mammals are described
below.
Stranding--In 2013, an International Scientific Review Panel
investigated a 2008 mass stranding of approximately 100 melon-headed
whales in a Madagascar lagoon system (Southall et al., 2013) associated
with the use of a high-frequency mapping system. The report indicated
that the use of a 12 kHz multi-beam echosounder was the most plausible
and likely initial behavioral trigger of the mass stranding event. This
was the first time that a relatively high-frequency mapping sonar
system has been associated with a stranding event. However, the report
also notes that there were several site- and situation-specific
secondary factors that may have contributed to the avoidance responses
that lead to the eventual entrapment and mortality of the whales within
the Loza Lagoon system (e.g., the survey vessel transiting in a north-
south direction on the shelf break parallel to the shore may have
trapped the animals between the sound source and the shore driving them
towards the Loza Lagoon). The report concluded that for odontocete
cetaceans that hear well in the 10 to 50 kHz range, where ambient noise
is typically quite low, high-power active sonars operating in this
range may be more easily audible and have potential effects over larger
areas than low-frequency systems that have more typically been
considered in terms of anthropogenic noise impacts (Southall et al.,
2013). However, the risk may be very low given the extensive use of
these systems worldwide on a daily basis and the lack of direct
evidence of such responses previously (Southall et al., 2013). It is
noted that leading scientific experts on multi-beam echosounders have
expressed concerns about the independent scientific review panel
analyses and findings (Bernstein, 2013).
Masking--Marine mammal communications would not be masked
appreciably by the multi-beam echosounder 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 multi-beam echosounder signals (12 kHz) generally do not
overlap with the predominant frequencies in the calls (16 Hz to less
than 12 kHz), which would avoid any significant masking (Richardson et
al., 1995).
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 (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 (656.2 ft) (Frankel, 2005). When a 38 kHz echosounder and a 150
kHz ADCP were transmitting during studies in the Eastern Tropical
Pacific, 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 second tonal signals at frequencies similar
to those that would be emitted by the multi-beam echosounder used by
SIO, 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 a multi-beam
echosounder.
Risch et al. (2012) found a reduction in humpback whale song in the
Stellwagen Bank National Marine Sanctuary during Ocean Acoustic
Waveguide Remote Sensing (OAWRS) activities that were carried out
approximately 200 km (108 nmi) away. The OAWRS used three frequency-
modulated pulses centered at frequencies of 415, 734, and 949 Hz with
received levels in the sanctuary of 88 to 110 dB re 1 [mu]Pa. Deng et
al. (2014) measured the spectral properties of pulses transmitted by
three 200 kHz echosounders, and found that they generated weaker sounds
at frequencies below the center frequency (90 to 130 kHz). These sounds
are within the hearing range of some marine mammals, and the authors
suggested that they could be strong enough to elicit behavioral
responses within close proximity to the sources, although they would be
well below potentially harmful levels.
Hearing Impairment and Other Physical Effects--Given several
stranding events that have been associated with the operation of naval
sonar in specific circumstances, there is concern that mid-frequency
sonar sounds can cause serious impacts to marine mammals (see above).
However, the multi-beam echosounder proposed for use by SIO is quite
different than sonar used for Navy operations. Pulse duration of the
multi-beam echosounder is very short relative to the naval sonar. Also,
at any given location, an individual marine mammal would be in the beam
of the multi-beam echosounder 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 and have higher
duty cycles. Those factors would all reduce the sound energy received
from the multi-beam echosounder rather drastically relative to that
from naval sonar. NMFS believes that the brief exposure of marine
mammals to one pulse, or small numbers of signals, from the multi-beam
echosounder in this particular case is not likely to result in the
harassment of marine mammals.
[[Page 15079]]
Sub-Bottom Profiler
SIO would operate a sub-bottom profiler (Knudsen 3260) from the
source vessel during the proposed study. Sounds from the sub-bottom
profiler are very short pulses, occurring for 1 to 4 ms once ever
second. Most of the energy in the sound pulses emitted by the sub-
bottom profiler is at frequencies 3.5 kHz, and the beam is directed
downward. The sub-bottom profiler that may be used on the Revelle has a
maximum source level of 204 dB re 1 [mu]Pa. The sonar emits energy in a
27[deg] beam from the bottom of the ship. Marine mammals that encounter
the Knudsen 3260 are unlikely to be subjected to repeated pulses
because of the relatively narrow fore-aft width of the beam and would
receive only limited amounts of pulse energy because of the short
pulses. Animals close to the ship (where the beam is narrowest) are
especially unlikely to be ensonified for more than one 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 a sub-bottom profiler emits a pulse is small--even for a
sub-bottom profiler more powerful than that that may be on the Revelle.
The animal would have to pass the transducer at close range and be
swimming at speeds similar to the vessel in order to receive the
multiple pulses that might result in sufficient exposure to cause TTS.
Navy sonars that have been linked to avoidance reactions and
stranding of cetaceans: (1) Generally have longer pulse duration than
the Knudsen 3260; and (2) are often directed close to horizontally
versus more downward for the sub-bottom profiler. The area of possible
influence of the single-beam 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 SIO's
operations, the individual pulses would be very short, and a given
mammal would not receive many of the downward-directed pulses as the
vessel passes by. Possible effects of a sub-bottom profiler on marine
mammals are described below.
Masking--Marine mammal communications would not be masked
appreciably by the sub-bottom profiler 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 baleen whales, the
sub-bottom profiler signals do not overlap with the predominant
frequencies in the calls (16 Hz to less than 12 kHz), which would avoid
any significant masking (Richardson et al., 1995).
Behavioral Responses--Marine mammal behavioral reactions to other
pulsed sound sources are discussed above, and responses to the sub-
bottom profiler are likely to be similar to those for other pulsed
sources if received at the same levels. However, the pulsed signals
from the sub-bottom profiler are considerably weaker than those from
the multi-beam 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 sub-bottom 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 sub-bottom profiler is
usually operated simultaneously with other higher-power acoustic
sources, including airguns. Many marine mammals will move away in
response to the approaching higher-power sources or the vessel itself
before the mammals would be close enough for there to be any
possibility of effects from the less intense sounds from the sub-bottom
profiler.
Heat-Flow Probe Deployment
During heat-flow measurements using a probe, the probe is a passive
instrument and no noise is created by the mechanical action of the
devices on the seafloor is not expected to be perceived by nearby fish
and other marine organisms. Heat-flow measurement activities would be
highly localized and short-term in duration and would not be expected
to significantly interfere with marine mammal behavior. The potential
direct effects include temporary localized disturbance or displacement
from associated physical movement/actions of the operations.
Additionally, the potential indirect effects may consist of very
localized and transitory/short-term disturbance of bottom habitat and
associated prey in shallow-water areas as a result of heat-flow probe
measurements. NMFS believes that the since the heat-flow probe is a
passive instrument and has no mechanical action, it would not likely
result in the harassment of marine mammals.
A maximum total of 200 heat-flow measurements would be obtained
using these devices and ranging from 1 to 2 hours per measurement (for
a total of approximately 320 hours of operations) and it is estimated
that the pinger would operate continuously during each heat-flow probe
deployment. The vessel would be stationary during heat-flow probe
deployment and repositioned to repeat the process, so the likelihood of
a collision or entanglement with a marine mammal is very low. For the
heat-flow measurements, the lance is 4.5 m and would disturb an area
approximately 8 cm x 20 cm (3.1 in x 7.9 in). Assuming approximately
200 heat-flow measurements, the cumulative area of seafloor that could
be disturbed during the proposed study would be approximately 32,000
cm\2\ (4,960 in\2\).
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 in 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
(especially low frequency specialists) 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
[[Page 15080]]
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' reaction varied when exposed to vessel noise and
traffic. In some cases, beluga whales exhibited rapid swimming from
ice-breaking vessels up to 80 km (43.2 nmi) away and showed changes in
surfacing, breathing, diving, and group composition in the Canadian
high Arctic where vessel traffic is rare (Finley et al., 1990). In
other cases, beluga whales were more tolerant of vessels, but responded
differentially to certain vessels and operating characteristics by
reducing their calling rates (especially older animals) in the St.
Lawrence River where vessel traffic is common (Blane and Jaakson,
1994). In Bristol Bay, Alaska, beluga whales continued to feed when
surrounded by fishing vessels and resisted dispersal even when
purposefully harassed (Fish and Vania, 1971).
In reviewing more than 25 years of whale observation data, Watkins
(1986) concluded that whale reactions to vessel traffic were ``modified
by their previous experience and current activity: Habituation often
occurred rapidly, attention to other stimuli or preoccupation with
other activities sometimes overcame their interest or wariness of
stimuli.'' Watkins noticed that over the years of exposure to ships in
the Cape Cod area, minke whales changed from frequent positive interest
(e.g., approaching vessels) to generally uninterested reactions; fin
whales changed from mostly negative (e.g., avoidance) to uninterested
reactions; 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 Revelle would be audible to
marine mammals over a large distance, it is unlikely that marine
mammals would respond behaviorally (in a manner that NMFS would
consider harassment under the MMPA) to low-level distant shipping noise
as the animals in the area are likely to be habituated to such noises
(Nowacek et al., 2004). In light of these facts, NMFS does not expect
the Revelle'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
dolphins) 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 13 kts (24.1 km/hr, 14.9 mph).
SIO's proposed operation of one source vessel for the proposed low-
energy seismic survey is relatively small in scale (i.e., a one vessel
operation) compared to the number of other ships (e.g., fishing,
tourist, and other vessels) transiting at higher speeds in the same
areas on an annual basis. The probability of vessel and marine mammal
interactions occurring during the proposed low-energy seismic survey is
unlikely due to the Revelle's slow operational speed, which is
typically 5 kts. Outside of seismic operations, the Revelle's cruising
speed would be approximately 10.1 to 14.5 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 Revelle has a number of other advantages for
avoiding ship strikes as compared to most commercial merchant vessels,
including the following: The Revelle's bridge and other observing
stations offer good visibility to visually monitor for marine mammal
presence; PSOs posted during operations scan the ocean for marine
mammals and must report visual alerts of marine mammal presence to
crew; and the PSOs 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 low-energy seismic survey would require
towing approximately one 600 m cable streamers. While towing this size
of an array carries some level of risk of entanglement for marine
mammals due to the operational nature of the activity, entanglement is
unlikely. 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. In May 2011, there
was one recorded entrapment of an olive ridley sea turtle (Lepidochelys
olivacea) in the R/V Marcus G. Langseth's barovanes after the
conclusion of a seismic survey off
[[Page 15081]]
Costa Rica. There have been cases of baleen whales, mostly gray whales
(Heyning, 1990), becoming entangled in fishing lines. The probability
for entanglement of marine mammals is considered very low because of
the vessel speed and the monitoring efforts onboard the survey vessel.
Furthermore, there has been no history of marine mammal entanglement
with seismic equipment used by the U.S. academic research fleet.
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
impact on affected marine mammal species and stocks.
Anticipated Effects on Marine Mammal Habitat
The proposed low-energy seismic survey is not anticipated to have
any permanent impact on habitats used by the marine mammals in the
proposed study area, including the food sources they use (i.e. fish and
invertebrates). Additionally, no physical damage to any habitat is
anticipated as a result of conducting airgun operations during the
proposed low-energy seismic survey. While it is anticipated that the
specified activity may result in marine mammals avoiding certain areas
due to brief, temporary ensonification, this impact to habitat is
temporary 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 in any particular area
of the approximately 1,154 km \2\ proposed study area, previously
discussed in this notice.
The next section discusses the potential impacts of anthropogenic
sound sources on common marine mammal prey in the proposed study 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 and
invertebrate 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. This makes drawing conclusions about impacts on fish problematic
because, ultimately, the most important issues concern effects on
marine fish populations, their viability, and their availability to
fisheries.
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.
There are only two known papers with proper experimental methods,
controls, and careful pathological investigation implicating sounds
produced by actual seismic survey airguns in causing adverse anatomical
effects. One such study indicated anatomical damage, and the second
indicated TTS in fish hearing. The anatomical case is McCauley et al.
(2003), who found that exposure to airgun sound caused observable
anatomical damage to the auditory maculae of pink snapper (Pagrus
auratus). This damage in the ears had not been repaired in fish
sacrificed and examined almost two months after exposure. On the other
hand, Popper et al. (2005) documented only TTS (as determined by
auditory brainstem response) in two of three fish species from the
Mackenzie River Delta. This study found that broad whitefish (Coregonus
nasus) exposed to five airgun shots were not significantly different
from those of controls. During both studies, the repetitive exposure to
sound was greater than would have occurred during a typical seismic
survey. However, the substantial 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 nine m in the former case and less than two m in
the latter). Water depth sets a lower limit on the lowest sound
frequency that would propagate (the ``cutoff frequency'') at about one-
quarter wavelength (Urick, 1983; Rogers and Cox, 1988).
Wardle et al. (2001) suggested that in water, acute injury and
death of organisms exposed to seismic energy depends primarily on two
features of the sound source: (1) The received peak pressure, and (2)
the time required for the pressure to rise and decay. Generally, as
received pressure increases, the period for the pressure to rise and
decay decreases, and the chance of acute pathological effects
increases. According to Buchanan et al.
[[Page 15082]]
(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). The airgun was suspended 3.5 m (11.5 ft)
above a school of threadfin shad in Lake Meade and was 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 death of any of the fish carcasses
observed. They also concluded that 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 former Minerals Management Service (MMS, 2005) assessed the
effects of a proposed seismic survey in Cook Inlet. The seismic survey
proposed using three vessels, each towing two four-airgun arrays
ranging from 24,580.6 to 40,967.7 cm\3\ (1,500 to 2,500 in\3\). MMS
noted that the impact to fish populations in the survey area and
adjacent waters would likely be very low and temporary. MMS 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 provided in Appendix D of NSF/USGS's PEIS
(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
[[Page 15083]]
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 species of cephalopods (Loligo
vulgaris, Sepia officinalis, Octopus vulgaris, and Ilex coindetii),
primarily cuttlefish, to two hours of continuous 50 to 400 Hz
sinusoidal wave sweeps at 157+/-5 dB re 1 [micro]Pa while captive in
relatively small tanks. They reported morphological and ultrastructural
evidence of massive acoustic trauma (i.e., permanent and substantial
alterations [lesions] of statocyst sensory hair cells) to the exposed
animals that increased in severity with time, suggesting that
cephalopods are particularly sensitive to low frequency sound. The
received SPL was reported as 157+/-5 dB re 1 [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, that 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). More information on the potential effects of airguns on fish
and invertebrates are reviewed in section 3.2.4.3, section 3.3.4.3, and
Appendix D of the NSF/USGS PEIS (2011).
Proposed Mitigation
In order to issue an Incidental Take Authorization (ITA) under
section 101(a)(5)(D) of the MMPA, NMFS must set forth the permissible
methods of taking pursuant to such activity, and other means of
effecting the least practicable 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 (where relevant).
SIO reviewed the following source documents and incorporated a
suite of appropriate mitigation measures into the project description.
(1) Protocols used during previous NSF and USGS-funded seismic
research cruises as approved by NMFS and detailed in the ``Final
Programmatic Environmental Impact Statement/Overseas Environmental
Impact Statement for Marine Seismic Research Funded by the National
Science Foundation or Conducted by the U.S. Geological Survey;''
(2) Previous IHA applications and IHAs approved and authorized by
NMFS; and
(3) Recommended best practices in Richardson et al. (1995), Pierson
et al. (1998), and Weir and Dolman, (2007).
To reduce the potential for disturbance from acoustic stimuli
associated with the activities, SIO proposed to implement the following
mitigation measures for marine mammals:
(1) Proposed exclusion zones around the sound source;
(2) Speed and course alterations;
(3) Shut-down procedures; and
(4) Ramp-up procedures.
Proposed Exclusion Zones--During pre-planning of the cruise, the
smallest airgun array was identified that could be used and still meet
the geophysical scientific objectives. SIO use radii to designate
exclusion and buffer zones and to estimate take for marine mammals.
Table 2 (presented earlier in this document) shows the distances at
which one would expect to receive three sound levels (160, 180, and 190
dB) from the two GI airgun array. The 180 and 190 dB level shut-down
criteria are applicable to cetaceans and pinnipeds, respectively, as
specified by NMFS (2000) and would be used to establish the exclusion
and buffer zones.
Received sound levels have been modeled by L-DEO for a number of
airgun configurations, including two 45 in \3\ Nucleus G airguns, in
relation to distance and direction from the airguns (see Figure 2 of
the IHA application). In addition, propagation measurements of pulses
from two GI airguns have been reported for shallow water (approximately
30 m [98.4 ft] depth) in the Gulf of Mexico (Tolstoy et al., 2004).
However, measurements were not made for the two GI airguns in deep
water. The model does not allow for bottom interactions, and is most
directly applicable to deep water. Based on the modeling, estimates of
the maximum distances from the GI airguns where sound levels are
predicted to be 190,
[[Page 15084]]
180, and 160 dB re 1 [micro]Pa (rms) in intermediate and deep water
were determined (see Table 2 above).
Empirical data concerning the 190, 180, and 160 dB (rms) distances
were acquired for various airgun arrays based on measurements during
the acoustic verification studies conducted by L-DEO in the northern
Gulf of Mexico in 2003 (Tolstoy et al., 2004) and 2007 to 2008 (Tolstoy
et al., 2009). Results of the 18 and 36 airgun arrays are not relevant
for the two GI airguns to be used in the proposed low-energy seismic
survey because the airgun arrays are not the same size or volume. The
empirical data for the 6, 10, 12, and 20 airgun arrays indicate that,
for deep water, the L-DEO model tends to overestimate the received
sound levels at a given distance (Tolstoy et al., 2004). Measurements
were not made for the two GI airgun array in deep water; however, SIO
proposes to use the safety radii predicted by L-DEO's model for the
proposed GI airgun operations in intermediate and deep water, although
they are likely conservative given the empirical results for the other
arrays.
Based on the modeling data, the outputs from the pair of 45 in \3\
GI airguns proposed to be used during the low-energy seismic survey are
considered a low-energy acoustic source in the NSF/USGS PEIS (2011) for
marine seismic research. A low-energy seismic source was defined in the
NSF/USGS PEIS as an acoustic source whose received level is less than
or equal to180 dB at 100 m (including any single or any two GI airguns
and a single pair of clustered airguns with individual volumes of less
than or equal to 250 in \3\). The NSF/USGS PEIS also established for
these low-energy sources a standard exclusion zone of 100 m for all
low-energy sources in water depths greater than 100 m. This standard
100 m exclusion zone would be used during the proposed low-energy
seismic survey using the pair of 45 in \3\ GI airguns. The 180 and 190
dB (rms) radii are the current Level A harassment shut-down criteria
applicable to cetaceans and pinnipeds, respectively; these levels were
used to establish exclusion zones. Therefore, the assumed 180 and 190
dB radii are 100 m for intermediate and deep water. If the PSO detects
a marine mammal within or about to enter the appropriate exclusion
zone, the airguns would be shut down immediately.
Speed and Course Alterations--If a marine mammal is detected
outside the exclusion zone and, based on its position and direction of
travel (relative motion), is likely to enter the exclusion zone,
changes of the vessel's speed and/or direct course would be considered
if this does not compromise operational safety or damage the deployed
equipment. This would be done if operationally practicable while
minimizing the effect on the planned science objectives. For marine
seismic surveys towing large streamer arrays, course alterations are
not typically implemented due to the vessel's limited maneuverability.
However, the Revelle would be towing a relatively short hydrophone
streamer, so its maneuverability during operations with the hydrophone
streamer would not be limited as vessels towing long streamers, thus
increasing the potential to implement course alterations, if necessary.
After any such speed and/or course alteration is begun, the marine
mammal activities and movements relative to the seismic vessel would be
closely monitored to ensure that the marine mammal does not approach
within the applicable exclusion zone. If the marine mammal appears
likely to enter the exclusion zone, further mitigation actions would be
taken, including further speed and/or course alterations, and/or shut-
down of the airgun(s). Typically, during airgun operations, the source
vessel is unable to change speed or course, and one or more alternative
mitigation measures would need to be implemented.
Shut-Down Procedures--If a marine mammal is detected outside the
exclusion zone for the airgun(s) but is likely to enter the exclusion
zone, and the vessel's speed and/or course cannot be changed to avoid
having the animal enter the exclusion zone, SIO would shut-down the
operating airgun(s) before the animal is within the exclusion zone.
Likewise, if a marine mammal is already within the exclusion zone when
first detected, the airguns would be shut-down immediately.
Following a shut-down, SIO would not resume airgun activity until
the marine mammal has cleared the exclusion zone, or until the PSO is
confident that the animal has left the vicinity of the vessel. SIO
would consider the animal to have cleared the exclusion zone if:
A PSO has visually observed the animal leave the exclusion
zone, or
A PSO has not sighted the animal within the exclusion zone
for 15 minutes for species with shorter dive durations (i.e., small
odontocetes and pinnipeds), or 30 minutes for species with longer dive
durations (i.e., mysticetes and large odontocetes, including sperm,
dwarf and pygmy sperm, killer, and beaked whales).
Although power-down procedures are often standard operating
practice for seismic surveys, they are not proposed to be used during
this planned low-energy seismic survey because powering down from two
airguns to one airgun would make only a small difference in the
exclusion zone(s) that probably would not be enough to allow continued
one-airgun operations if a marine mammal came within the exclusion zone
for two airguns.
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, avoiding any potential injury or impairment
of their hearing abilities. SIO would follow a ramp-up procedure when
the airgun array begins operating after a specified period without
airgun operations or when a shut-down has exceeded that period. SIO
proposes that, for the present cruise, this period would be
approximately 15 minutes. SIO, L-DEO, USGS, NSF, and ASC have used
similar periods (approximately 15 minutes) during previous low-energy
seismic surveys.
Ramp-up would begin with a single GI airgun (45 in \3\). The second
GI airgun (45 in \3\) would be added after 5 minutes. During ramp-up,
the PSOs would monitor the exclusion zone, and if marine mammals are
sighted, a shut-down would be implemented as though both GI airguns
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, SIO would not commence the ramp-up. Given these provisions,
it is likely that the airgun array would not be ramped-up from a
complete shut-down during low light conditions, at night, or in thick
fog, (i.e., poor visibility conditions) because the outer part of the
exclusion zone for that array would not be visible during those
conditions. If one airgun has been operating, ramp-up to full power
would be permissible during low light, 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 if they choose. SIO would not initiate a ramp-up of the
airguns if a marine mammal is sighted within or near the applicable
exclusion zones during day or night. NMFS refers the reader to Figure
2, which presents a flowchart representing the ramp-up and shut-down
protocols described in this notice.
BILLING CODE 3510-22-P
[[Page 15085]]
[GRAPHIC] [TIFF OMITTED] TN20MR15.001
BILLING CODE 3510-22-C
Proposed Mitigation Conclusions
NMFS has carefully evaluated the applicant's proposed mitigation
measures and has considered a range of other measures in the context of
ensuring that NMFS prescribes the means of effecting the least
practicable impact on the affected marine mammal species and stocks and
their habitat. NMFS's evaluation of potential measures included
consideration of the following factors in relation to one another:
(1) The manner in which, and the degree to which, the successful
implementation of the measure is expected to minimize adverse impacts
to marine mammals;
(2) The proven or likely efficacy of the specific measure to
minimize adverse impacts as planned; and
(3) The practicability of the measure for applicant implementation.
Any mitigation measure(s) prescribed by NMFS should be able to
accomplish, have a reasonable likelihood of accomplishing (based on
current science), or contribute to the accomplishment of one or more of
the general goals listed below:
(1) Avoidance of minimization of injury or death of marine mammals
wherever possible (goals 2, 3, and 4 may contribute to this goal).
(2) A reduction in the numbers of marine mammals (total number or
[[Page 15086]]
number at biologically important time or location) exposed to received
levels of airguns, or other activities expected to result in the take
of marine mammals (this goal may contribute to 1, above, or to reducing
harassment takes only).
(3) A reduction in the number of time (total number or number at
biologically important time or location) individuals would be exposed
to received levels of airguns, or other activities expected to result
in the take of marine mammals (this goal may contribute to 1, above, or
to reducing harassment takes only).
(4) A reduction in the intensity of exposures (either total number
or number at biologically important time or location) to received
levels of airguns, or other activities, or other activities expected to
result in the take of marine mammals (this goal may contribute to a,
above, or to reducing the severity of harassment takes only).
(5) Avoidance or minimization of adverse effects to marine mammal
habitat, paying special attention to the food base, activities that
block or limit passage to or from biologically important areas,
permanent destruction of habitat, or temporary destruction/disturbance
of habitat during a biologically important time.
(6) For monitoring directly related to mitigation--an increase in
the probability of detecting marine mammals, thus allowing for more
effective implementation of the mitigation.
Based on NMFS's evaluation of the applicant's proposed measures, as
well as other measures considered by NMFS or recommended by the public,
NMFS has preliminarily determined that the proposed mitigation measures
provide the means of effecting the least practicable impact on marine
mammal species or stocks and their habitat, paying particular attention
to rookeries, mating grounds, and areas of similar significance.
Proposed Monitoring and Reporting
In order to issue an ITA for an activity, section 101(a)(5)(D) of
the MMPA states that NMFS must set forth ``requirements pertaining to
the monitoring and reporting of such taking.'' The MMPA implementing
regulations at 50 CFR 216.104(a)(13) indicate that requests for IHAs
must include the suggested means of accomplishing the necessary
monitoring and reporting that would result in increased knowledge of
the species and of the level of taking or impacts on populations of
marine mammals that are expected to be present in the proposed action
area. SIO submitted a marine mammal monitoring plan as part of the IHA
application. It can be found in Section 13 of the IHA application. The
plan may be modified or supplemented based on comments or new
information received from the public during the public comment period.
Monitoring measures prescribed by NMFS should accomplish one or
more of the following general goals:
(1) An increase in the probability of detecting marine mammals,
both within the mitigation zone (thus allowing for more effective
implementation of the mitigation) and in general to generate more data
to contribute to the analyses mentioned below;
(2) An increase in our understanding of how many marine mammals are
likely to be exposed to levels of sound (airguns) that we associate
with specific adverse effects, such as behavioral harassment, TTS, or
PTS;
(3) An increase in our understanding of how marine mammals respond
to stimuli expected to result in take and how anticipated adverse
effects on individuals (in different ways and to varying degrees) may
impact the population, species, or stock (specifically through effects
on annual rates of recruitment or survival) through any of the
following methods:
Behavioral observations in the presence of stimuli
compared to observations in the absence of stimuli (need to be able to
accurately predict received level, distance from source, and other
pertinent information);
Physiological measurements in the presence of stimuli
compared to observations in the absence of stimuli (need to be able to
accurately predict received level, distance from source, and other
pertinent information); and
Distribution and/or abundance comparisons in times or
areas with concentrated stimuli versus times or areas without stimuli;
(4) An increased knowledge of the affected species; and
(5) An increase in our understanding of the effectiveness of
certain mitigation and monitoring measures.
Proposed Monitoring
SIO proposes to sponsor marine mammal monitoring during the
proposed project, in order to implement the proposed mitigation
measures that require real-time monitoring and to satisfy the
anticipated monitoring requirements of the IHA. SIO's proposed
``Monitoring Plan'' is described below this section. The monitoring
work described here has been planned as a self-contained project
independent of any other related monitoring projects that may be
occurring simultaneously in the same regions. SIO is prepared to
discuss coordination of their monitoring program with any related work
that might be done by other groups insofar as this is practical and
desirable.
Vessel-Based Visual Monitoring
PSOs would be based aboard the seismic source vessel and would
watch for marine mammals near the vessel during daytime airgun
operations and during any ramp-ups of the airguns at night. PSOs would
also watch for marine mammals near the seismic vessel for at least 30
minutes prior to the start of airgun operations and after an extended
shut-down (i.e., greater than approximately 15 minutes for this
proposed low-energy seismic survey). When feasible, PSOs would conduct
observations during daytime periods when the seismic system is not
operating (such as during transits) for comparison of sighting rates
and behavior with and without airgun operations and between acquisition
periods. Based on PSO observations, the airguns would be shut-down when
marine mammals are observed within or about to enter a designated
exclusion zone.
During airgun operations in the Southwest Pacific Ocean, East of
New Zealand, at least three PSOs would be based aboard the Revelle. At
least one PSO would stand watch at all times while the Revelle is
operating airguns during the proposed low-energy seismic survey; this
procedure would also be followed when the vessel is in transit. SIO
would appoint the PSOs with NMFS's concurrence. The lead PSO would be
experienced with marine mammal species in the Pacific Ocean and/or off
the east coast of New Zealand, the second and third PSOs would receive
additional specialized training from the lead PSO to ensure that they
can identify marine mammal species commonly found in the Southwest
Pacific Ocean. Observations would take place during ongoing daytime
operations and ramp-ups of the airguns. During the majority of seismic
operations, at least one PSO would be on duty from observation
platforms (i.e., the best available vantage point on the source vessel)
to monitor marine mammals near the seismic vessel. PSO(s) would be on
duty in shifts no longer than 4 hours in duration. Other crew would
also be instructed to assist in detecting marine mammals and
implementing mitigation requirements (if practical). Before the start
of the low-energy seismic survey, the crew would be given additional
instruction on how to do so.
The Revelle is a suitable platform for marine mammal observations
and
[[Page 15087]]
would serve as the platform from which PSOs would watch for marine
mammals before and during airgun operations. The Revelle has been used
for marine mammal observations during the routine California
Cooperative Oceanic Fisheries Investigations (CalCOFI). Two locations
are likely as observation stations onboard the Revelle. Observing
stations are located at the 02 level, with PSO eye level at
approximately 10.4 m (34 ft) above the waterline and the PSO would have
a good view around the entire vessel. At a forward-centered position on
the 02 deck, the view is approximately 240[deg] around the vessel; and
one atop the aft hangar, with an aft-centered view includes the 100 m
radius around the GI airguns. The PSO eye level on the bridge is
approximately 15 m (49.2 ft) above sea level. PSOs would work on the
enclosed bridge and adjoining aft steering station during any inclement
weather.
Standard equipment for PSOs would be reticle binoculars and optical
range finders. Night-vision equipment would be available at night and
low-light conditions during the cruise. The PSOs would be in
communication with ship's officers on the bridge and scientists in the
vessel's operations laboratory, so they can advise promptly of the need
for avoidance maneuvers or seismic source shut-down. During daylight,
the PSO(s) would scan the area around the vessel systematically with
reticle binoculars (e.g., 7 x 50 Fujinon FMTRC-SX), Big-eye binoculars
(e.g., 25 x 150 Fujinon MT), optical range-finders (to assist with
distance estimation), and the naked eye. These binoculars would have a
built-in daylight compass. Estimating distances is done primarily with
the reticles in the binoculars. The optical range-finders are useful in
training PSOs to estimate distances visually, but are generally not
useful in measuring distances to animals directly. At night, night-
vision equipment would be available. The PSO(s) would be in direct
(radio) wireless communication with ship's officers on the bridge and
scientists in the vessel's operations laboratory during seismic
operations, so they can advise the vessel operator, science support
personnel, and the science party promptly of the need for avoidance
maneuvers or a shut-down of the seismic source.
When a marine mammal is detected within or about to enter the
designated exclusion zone, the airguns would immediately be shut-down,
unless the vessel's speed and/or course can be changed to avoid having
the animal enter the exclusion zone. The PSO(s) would continue to
maintain watch to determine when the animal is outside the exclusion
zone by visual confirmation. Airgun operations would not resume until
the animal is confirmed to have left the exclusion zone, or is 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,
dwarf and pygmy sperm, killer, and beaked whales).
PSO Data and Documentation
PSOs 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. Data would be used to estimate
numbers of animals potentially ``taken'' by harassment. They would also
provide information needed to order a shut-down of the airguns when a
marine mammal is within or near the exclusion zone. Observations would
also be made during daylight periods when the Revelle is underway
without seismic airgun operations (i.e., transits to, from, and through
the study area) to collect baseline biological data.
When a sighting is made, the following information about the
sighting would be recorded:
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 seismic source or vessel (e.g., none,
avoidance, approach, paralleling, etc.), and behavioral pace.
2. Time, location, heading, speed, activity of the vessel
(including number of airguns operating and whether in state of ramp-up
or shut-down), sea state, wind force, visibility, cloud cover, and sun
glare.
The data listed under (2) would also be recorded at the start and
end of each observation watch, and during a watch whenever there is a
change in one or more of the variables.
All observations, as well as information regarding ramp-ups or
shut-downs, would be recorded in a standardized format. Data would be
entered into an electronic database. The data accuracy would be
verified by computerized data validity checks as the data are entered
and by subsequent manual checking of the database by the PSOs at sea.
These procedures would allow initial summaries of data to be prepared
during and shortly after the field program, and would facilitate
transfer of the data to statistical, graphical, and other programs for
further processing and archiving.
Results from the vessel-based observations would provide the
following information:
1. The basis for real-time mitigation (airgun shut-down).
2. Information needed to estimate the number of marine mammals
potentially taken by harassment, which must be reported to NMFS.
3. Data on the occurrence, distribution, and activities of marine
mammals in the area where the seismic study is conducted.
4. Information to compare the distance and distribution of marine
mammals relative to the source vessel at times with and without airgun
operations.
5. Data on the behavior and movement patterns of marine mammals
seen at times with and without airgun operations.
Proposed Reporting
SIO would submit a comprehensive report to NMFS and NSF within 90
days after the end of the cruise. The report would describe the
operations that were conducted and sightings of marine mammals near the
operations. The report submitted to NMFS and NSF would provide full
documentation of methods, results, and interpretation pertaining to all
monitoring. The 90-day report would summarize the dates and locations
of airgun operations and all marine mammal sightings (i.e., dates,
times, locations, activities, and associated seismic survey
activities). The report would include, at a minimum:
Summaries of monitoring effort--total hours, total
distances, and distribution of marine mammals through the study period
accounting for Beaufort sea state and other factors affecting
visibility and detectability of marine mammals;
Analyses of the effects of various factors influencing
detectability of marine mammals including Beaufort sea state, number of
PSOs, and fog/glare;
Species composition, occurrence, and distribution of
marine mammals sightings including date, water depth, numbers, age/
size/gender, and group sizes, and analyses of the effects of airgun
operations;
Sighting rates of marine mammals during periods with and
without airgun operations (and other variables that could affect
detectability);
Initial sighting distances versus airgun operations state;
Closest point of approach versus airgun operations state;
[[Page 15088]]
Observed behaviors and types of movements versus airgun
operations activity state;
Numbers of sightings/individuals seen versus airgun
operations state; and
Distribution around the source vessel versus airgun
operations state.
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. NMFS would review the draft report and
provide any comments it may have, and SIO would incorporate NMFS's
comments and prepare a final report. After the report is considered
final, it would be publicly available on the NMFS Web site at: https://www.nmfs.noaa.gov/pr/permits/incidental/.
Reporting Prohibited Take--In the unanticipated event that the
specified activity clearly causes the take of a marine mammal in a
manner prohibited by this IHA, such as an injury (Level A harassment),
serious injury or mortality (e.g., ship-strike, gear interaction, and/
or entanglement), SIO would immediately cease the specified activities
and immediately report the incident to the Chief of the Permits and
Conservation Division, Office of Protected Resources, NMFS at 301-427-
8401 and/or by email to Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov. The report must include the following
information:
Time, date, and location (latitude/longitude) of the
incident;
Name and type of vessel involved;
Vessel's speed during and leading up to the incident;
Description of the incident;
Status of all sound source use in the 24 hours preceding
the incident;
Water depth;
Environmental conditions (e.g., wind speed and direction,
Beaufort sea state, cloud cover, and visibility);
Description of all marine mammal observations in the 24
hours preceding the incident;
Species identification or description of the animal(s)
involved;
Fate of the animal(s); and
Photographs or video footage of the animal(s) (if
equipment is available).
Activities shall not resume until NMFS is able to review the
circumstances of the prohibited take. NMFS shall work with SIO to
determine what is necessary to minimize the likelihood of further
prohibited take and ensure MMPA compliance. SIO may not resume their
activities until notified by NMFS via letter or email, or telephone.
Reporting an Injured or Dead Marine Mammal With an Unknown Cause of
Death--In the event that SIO discover an injured or dead marine mammal,
and the lead PSO determines that the cause of the injury or death is
unknown and the death is relatively recent (i.e., in less than a
moderate state of decomposition), SIO shall immediately report the
incident to the Chief of the Permits and Conservation Division, Office
of Protected Resources, NMFS, at 301-427-8401, and/or by email to
Jolie.Harrison@noaa.gov and Howard.Goldstein@noaa.gov. The report must
include the same information identified in the paragraph above.
Activities may continue while NMFS reviews the circumstances of the
incident. NMFS shall work with SIO to determine whether modifications
in the activities are appropriate.
Reporting an Injured or Dead Marine Mammal Not Related to the
Activities--In the event that SIO discovers an injured or dead marine
mammal, and the lead PSO determines that the injury or death is not
associated with or related to the activities authorized in the IHA
(e.g., previously wounded animal, carcass with moderate or advanced
decomposition, or scavenger damage), SIO shall report the incident to
the Chief of the Permits and Conservation Division, Office of Protected
Resources, NMFS, at 301-427-8401, and/or by email to
Jolie.Harrison@noaa.gov and Howard.Goldstein@noaa.gov, within 24 hours
of discovery. SIO shall provide photographs or video footage (if
available) or other documentation of the stranded animal sighting to
NMFS. Activities may continue while NMFS reviews the circumstances of
the incident.
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].
Table 4--NMFS's Current Underwater Acoustic Exposure Criteria
------------------------------------------------------------------------
Criterion
Criterion definition Threshold
------------------------------------------------------------------------
Impulsive (non-explosive) sound
------------------------------------------------------------------------
Level A harassment (injury)..... Permanent 180 dB re 1 [mu]Pa-
threshold shift m (root means
(PTS) (Any level square [rms])
above that which (cetaceans)
is known to cause 190 dB re 1 [mu]Pa-
TTS). m (rms)
(pinnipeds)
Level B harassment.............. Behavioral 160 dB re 1 [mu]Pa-
disruption (for m (rms)
impulsive noise).
Level B harassment.............. Behavioral 120 dB re 1 [mu]Pa-
disruption (for m (rms)
continuous noise).
------------------------------------------------------------------------
Level B harassment is anticipated and proposed to be authorized as
a result of the proposed low-energy seismic survey in the Southwest
Pacific Ocean, East of New Zealand. Acoustic stimuli (i.e., increased
underwater sound) generated during the operation of the seismic airgun
array are expected to result in the behavioral disturbance of some
marine mammals. NMFS's current underwater exposure criteria for
impulsive sound are detailed in Table 4 (above). There is no evidence
that the planned activities for which SIO seek the IHA could result in
injury, serious injury, or mortality. The required mitigation and
monitoring measures would minimize any potential risk for injury,
serious injury, or mortality.
The following sections describe SIO's methods to estimate take by
incidental harassment and present the applicant's estimates of the
numbers of marine mammals that could be affected. The estimates are
based on a consideration of the number of marine mammals that could be
harassed during the approximately 135 hours and 1,250 km of seismic
airgun operations with the two GI airgun array to be used.
There are no known systematic aircraft- or ship-based surveys
conducted for marine mammals stock assessments and very limited
population information available for marine mammals in offshore waters
of the Southwest Pacific Ocean off the east coast of New Zealand. For
most cetacean species, SIO and NMFS used densities from extensive NMFS
Southwest Fisheries Science Center (SWFSC) cruises (Ferguson and
Barlow, 2001, 2003; Barlow, 2003, 2010; Forney, 2007) in one province
of Longhurst's
[[Page 15089]]
(2006) pelagic biogeography, the California Current Province (CALC).
That province is similar to the South Subtropical Convergence Province
(SSTC) in which the proposed low-energy seismic survey is located, in
that productivity is high and large pelagic fish such as tuna occur.
Specifically, SIO and NMFS used the 1986 to 1996 data from blocks 35,
36, 47, 48, 59, and 60 of Ferguson and Barlow (2001, 2003), the 2001
data from Barlow (2003) for the Oregon, Washington, and California
strata, and the 2005 and 2008 data from Forney (2007) and Barlow
(2010), respectively, for the two strata combined. The densities used
were effort-weighted means for the 10 locations (blocks or States). The
surveys off California, Oregon, and Washington were conducted up to
approximately 556 km (300.2 nmi) offshore, and most of those data were
from offshore areas that overlap with the above blocks selected from
Ferguson and Barlow (2001, 2003).
For pinnipeds, SIO and NMFS used the densities in Bonnell et al.
(1992) of northern fur seals (Callorhinus ursinus) and northern
elephant seals in offshore areas of the western U.S. (the only species
regularly present in offshore areas there) to estimate the numbers of
pinnipeds that might be present off New Zealand.
The marine mammal species that would be encountered during the
proposed low-energy seismic survey would be different from those
sighted during surveys off the western U.S. and in the Eastern Tropical
Pacific Ocean. However, the overall abundances of species groups with
generally similar habitat requirements are expected to be roughly
similar. Thus, SIO and NMFS used the data described above to estimate
the group densities of beaked whales, delphinids, small whales, and
mysticetes in the proposed study area. SIO and NMFS then estimated the
relative abundance of individual southern species within the species
groups using various surveys and other information from areas near the
study area, and general information on species' distributions such as
latitudinal ranges and group sizes. Group densities from northern
species were multiplied by their estimated relative abundance off New
Zealand divided by the relative abundance for all species in the
species group to derive estimates for the southern species (see Table 3
of the IHA application).
Densities for several cetacean species are available for the
Southern Ocean (Butterworth et al., 1994), as follows: (1) For
humpback, sei, fin, blue, sperm, killer, and pilot whales in Antarctic
Management areas I to VI south of 60[deg] South, based on the 1978/1979
to 1984 and 1985/1986 to 1990/1991 IWC/IDCR circumpolar sighting survey
cruises, and (2) for humpback, sei, fin, blue, and sperm whales
extrapolated to latitudes 30 to 40[deg] South, 40 to 50[deg] South, 50
to 60[deg] South based on Japanese scouting vessel data from 1965/1966
to 1977/1978 and 1978/1979 to 1987/1988. SIO and NMFS calculated
densities based on abundance and surface areas given in Butterworth et
al. (1994) and used the weighted or mean density for the Regions V and/
or VI (whichever is available) due to locations that represent foraging
areas or distributions for animals that are likely to move past New
Zealand during northerly migrations or breed in New Zealand waters.
The densities used for purposes of estimating potential take do not
take into account the patchy distributions of marine mammals in an
ecosystem, at least on the moderate to fine scales over which they are
known to occur. Instead, animals are considered evenly distributed
throughout the assessed study area and seasonal movement patterns are
not taken into account, as none are available. Although there is some
uncertainty about the representativeness of the data and the
assumptions used in the calculations below, the approach used here is
believed to be the best available approach, using the best available
science.
Table 5--Estimated Densities and Possible Number of Marine Mammal Species That Might Be Exposed to Greater Than or Equal to 160 dB (Airgun Operations)
During SIO's Proposed Low-Energy Seismic Survey (Approximately 1,250 km of Tracklines/Approximately 1,154 km \2\ Ensonified Area for Airgun Operations)
in the Southwest Pacific Ocean, East of New Zealand, May to June 2015
--------------------------------------------------------------------------------------------------------------------------------------------------------
Calculated
take from
seismic airgun
Density U.S. operations
West Coast/ (i.e., Approximate
Southern Ocean/ estimated Proposed take percentage of
Species estimate used number of authorization Abundance \4\ population estimate Population trend \6\
(number of individuals \3\ (proposed take) \5\
animals/1,000 exposed to
km\2\) \1\ sound levels
>=160 dB re 1
[mu]Pa) \2\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Mysticetes
--------------------------------------------------------------------------------------------------------------------------------------------------------
Southern right whale............... 0.98/NA/0.98 1.13 2 8,000 to 15,000-- 0.03--Worldwide. Increasing at 7 to 8%
Worldwide. 12,000-- 0.02--Southern per year.
Southern Hemisphere. Hemisphere. 0.07--
2,700--Sub-Antarctic Sub-Antarctic New
New Zealand. Zealand.
Pygmy right whale.................. 0.39/NA/0.39 0.45 2 NA................... NA................... NA.
Humpback whale..................... 0.98/0.25/0.25 0.29 2 35,000 to 42,000-- <0.01--Southern Increasing.
Southern Hemisphere. Hemisphere.
Antarctic minke whale.............. 0.59/NA/0.59 0.68 2 720,000 to 750,000-- <0.01--Southern Stable.
Southern Hemisphere. Hemisphere.
[[Page 15090]]
Minke whale (including dwarf minke 0.59/NA/0.59 0.68 2 720,000 to 750,000-- <0.01--Southern NA.
whale sub-species). Southern Hemisphere. Hemisphere.
Bryde's whale...................... 0.20/NA/0.20 0.23 2 At least 30,000 to <0.01--Worldwide. NA.
40,000--Worldwide. <0.01--Northwestern
21,000--Northwestern Pacific Ocean <0.01.
Pacific Ocean 48,109.
Sei whale.......................... 0.59/0.08/0.08 0.09 2 80,000--Worldwide. <0.01--Worldwide. NA.
10,000--South of 0.02--South of
Antarctic Antarctic
Convergence. Convergence.
Fin whale.......................... 0.59/0.13/0.13 0.15 2 140,000--Worldwide. <0.01--Worldwide. NA.
15,000--South of 0.01--South of
Antarctic Antarctic
Convergence. Convergence.
Blue whale......................... 0.59/0.05/0.05 0.06 2 8,000 to 9,000-- 0.03--Worldwide. NA.
Worldwide. 2,300-- 0.09--True Southern
True Southern Hemisphere. 0.13--
Hemisphere. 1,500-- Pygmy.
Pygmy.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Odontocetes
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sperm whale........................ 1.62/1.16/1.16 1.34 10 360,000--Worldwide. <0.01--Worldwide. NA.
30,000--South of 0.03--South of
Antarctic Antarctic
Convergence. Convergence.
Pygmy sperm whale.................. 0.97/NA/0.97 1.12 5 NA................... NA................... NA.
Cuvier's beaked whale.............. 0.69/NA/0.69 0.80 2 600,000.............. <0.01................ NA
Shepherd's beaked whale............ 0.46/NA/0.46 0.53 3 600,000.............. <0.01................ NA.
Southern bottlenose whale.......... 0.46/NA/0.46 0.53 2 50,000--South of <0.01--South of NA.
Antarctic Antarctic
Convergence 600,000. Convergence <0.01.
Andrew's beaked whale.............. 0.46/NA/0.46 0.53 2 600,000.............. <0.01................ NA.
Blainville's beaked whale.......... 0.23/NA/0.23 0.27 2 600,000.............. <0.01................ NA.
Gray's beaked whale................ 0.92/NA/0.92 1.06 2 600,000.............. <0.01................ NA.
Hector's beaked whale.............. 0.46/NA/0.46 0.53 2 600,000.............. <0.01................ NA.
Spade-toothed beaked whale......... 0.23/NA/0.23 0.27 2 600,000.............. <0.01................ NA.
Strap-toothed beaked whale......... 0.69/NA/0.69 0.80 3 600,000.............. <0.01................ NA.
Killer whale....................... 0.45/5.70/5.70 6.58 12 80,000--South of 0.02--South of NA.
Antarctic Antarctic
Convergence. Convergence.
False killer whale................. 0.27/NA/0.27 0.31 10 NA................... NA................... NA.
[[Page 15091]]
Long-finned pilot whale............ 0.27/6.41/6.41 7.40 20 200,000--South of 0.01--South of NA.
Antarctic Antarctic
Convergence. Convergence.
Short-finned pilot whale........... 0.45/NA/0.45 0.52 20 At least 600,000-- <0.01--Worldwide..... NA.
Worldwide.
Bottlenose dolphin................. 81.55/NA/81.55 94.11 95 At least 614,000-- 0.02--Worldwide...... NA.
Worldwide.
Dusky dolphin...................... 81.55/NA/81.55 94.11 95 12,000 to 20,000--New 0.79--New Zealand.... NA.
Zealand.
Hector's dolphin................... 32.62/NA/32.62 37.64 38 7,400................ 0.51................. Declining.
Hourglass dolphin.................. 48.93/NA/48.93 56.47 57 144,000 to 150,000-- 0.04--South of NA.
South of Antarctic Antarctic
Convergence. Convergence.
Short-beaked common dolphin........ 163.10/NA/ 188.22 189 At least 3,500,000-- <0.01--Worldwide..... NA.
163.10 Worldwide.
Southern right whale dolphin....... 48.93/NA/48.93 56.46 57 NA................... NA................... NA.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Pinnipeds
--------------------------------------------------------------------------------------------------------------------------------------------------------
Southern elephant seal............. 5.11/NA/5.11 5.90 6 640,000 to 650,000-- <0.01--Worldwide or Increasing,
Worldwide. 470,000-- South Georgia Island. decreasing, or
South Georgia Island stable depending on
607,000. breeding population.
New Zealand fur seal............... 12.79/NA/12.79 14.76 15 135,000--Worldwide. 0.01--Worldwide. Increasing.
50,000 to 100,000-- 0.03--New Zealand.
New Zealand.
--------------------------------------------------------------------------------------------------------------------------------------------------------
NA = Not available or not assessed.
\1\ Densities based on sightings from NMFS SWFSC, IWC, and Bonnell et al. (2012) data.
\2\ Calculated take is estimated density multiplied by the area ensonified to 160 dB (rms) around the proposed seismic tracklines, increased by 25% for
contingency.
\3\ Adjusted to account for average group size.
\4\ See population estimates for marine mammal species in Table 3 (above).
\5\ Total proposed authorized takes expressed as percentages of the species or regional populations.
\6\ Jefferson et al. (2008).
Numbers of marine mammals that might be present and potentially
disturbed are estimated based on the available data about marine mammal
distribution and densities in the U.S. west coast and Southern Ocean as
a proxy for the proposed study area off the east coast of New Zealand.
SIO estimated the number of different individuals that may be exposed
to airgun sounds with received levels greater than or equal to 160 dB
re 1 [micro]Pa (rms) for seismic airgun operations 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 in the area (in the
absence of the low-energy seismic survey). The number of possible
exposures can be estimated by considering the total marine area that
would be within the 160 dB radius (the diameter is 400 m multiplied by
2 for deep water depths, the diameter is 600 m multiplied by 2 for
intermediate water depths) around the operating airguns, including
areas of overlap. The spacing of tracklines is 500 m (1,640.4 ft) in
the smaller grids and 1,250 m (4,101.1 ft) in the larger grids. Overlap
was measured using GIS and was minimal (area with overlap is equal to
1.13 multiplied by the area without overlap). The take estimates were
calculated without overlap. The 160 dB radii are based on acoustic
modeling data for the airguns that may be used during the proposed
action (see SIO's IHA application). During the proposed low-energy
seismic survey, the transect lines are widely spaced relative to the
160 dB distance. As summarized in Table 2 (see Table 1 and Figure 2 of
the IHA application), the modeling results for the proposed low-energy
seismic airgun array indicate the received levels are dependent on
water depth. Since the majority of the proposed airgun operations would
be conducted in
[[Page 15092]]
waters 100 to 1,000 m deep or greater than 1,000 m deep, the buffer
zone of 600 m or 400 m, respectively, for the two 45 in\3\ GI airguns
was used.
The number of different individuals potentially exposed to received
levels greater than or equal to 160 dB re 1 [micro]Pa (rms) from
seismic airgun operations 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 (excluding overlap).
The area expected to be ensonified was determined by entering the
planned tracklines into MapInfo GIS using the GIS to identify the
relevant areas by ``drawing'' the applicable 160 dB (rms) isopleth
around each trackline, and then calculating the total area within the
isopleth. Applying the approach described above, approximately 1,153.6
km\2\ (including the 25% contingency [approximately 923 km\2\ without
contingency]) would be ensonified within the 160 dB isopleth for
seismic airgun operations on one or more occasions during the proposed
low-energy seismic survey. The total ensonified area (1,154 km\2\
[336.5 nmi\2\]) was calculated by adding 847 km\2\ (246.9 nmi\2\) in
deep water, 76 km\2\ (22.2 nmi\2\), and 230.8 km\2\ (67.3 nmi\2\) for
the 25% contingency. The take calculations within the study sites do
not explicitly add animals to account for the fact that new animals
(i.e., turnover) not accounted for in the initial density snapshot
could also approach and enter the area ensonified above 160 dB for
seismic airgun operations. However, studies suggest that many marine
mammals would avoid exposing themselves to sounds at this level, which
suggests that there would not necessarily be a large number of new
animals entering the area once the seismic survey started. Because this
approach for calculating take estimates does not account for turnover
in the marine mammal populations in the area during the course of the
proposed low-energy seismic survey, the actual number of individuals
exposed may be underestimated. However, any underestimation is likely
offset by the conservative (i.e., probably overestimated) line-
kilometer distances (including the 25% contingency) used to calculate
the survey area, and the fact the approach assumes that no cetaceans or
pinnipeds would move away or toward the tracklines as the Revelle
approaches in response to increasing sound levels before the levels
reach 160 dB for seismic airgun operations, which is likely to occur
and which would decrease the density of marine mammals in the survey
area. Another way of interpreting the estimates in Table 6 is that they
represent the number of individuals that would be expected (in absence
of a seismic program) to occur in the waters that would be exposed to
greater than or equal to 160 dB (rms) for seismic airgun operations.
SIO's estimates of exposures to various sound levels assume that
the proposed low-energy seismic survey would be carried out in full;
however, the ensonified areas calculated using the planned number of
line-kilometers has been increased by 25% to accommodate lines that may
need to be repeated, equipment testing, etc. As is typical during
offshore seismic surveys, inclement weather and equipment malfunctions
would be likely to cause delays and may limit the number of useful
line-kilometers of airgun operations that can be undertaken. The
estimates of the numbers of marine mammals potentially exposed to 160
dB (rms) received levels are precautionary and probably overestimate
the actual numbers of marine mammals that could be involved. These
estimates assume that there would be no weather, equipment, or
mitigation delays that limit the airgun operations, which is highly
unlikely.
Table 5 shows the estimates of the number of different individual
marine mammals anticipated to be exposed to greater than or equal to
160 dB re 1 [mu]Pa (rms) for seismic airgun operations during the low-
energy seismic survey if no animals moved away from the survey vessel.
The total proposed take authorization is given in the column that is
fourth from the left of Table 5.
Encouraging and Coordinating Research
SIO and NSF would coordinate the planned marine mammal monitoring
program associated with the proposed low-energy seismic survey with
other parties that express interest in this activity and area. SIO and
NSF would coordinate with applicable U.S. agencies (e.g., NMFS) and the
government of New Zealand, and would comply with their requirements.
The proposed low-energy seismic survey falls under Level 3 of the
``Code of Conduct for minimizing acoustic disturbance to marine mammals
from seismic survey operations'' issued by New Zealand. Level 3 seismic
surveys are exempt from the provisions of the Code of Conduct.
Impact on Availability of Affected Species or Stock for Taking for
Subsistence Uses
Section 101(a)(5)(D) of the MMPA also requires NMFS to determine
that the authorization would not have an unmitigable adverse impact on
the availability of marine mammal species or stocks for subsistence
use. There are no relevant subsistence uses of marine mammals
implicated by this action (in the Southwest Pacific Ocean, East of New
Zealand study area). Therefore, NMFS has determined that the total
taking of affected species or stocks would not have an unmitigable
adverse impact on the availability of such species or stocks for taking
for subsistence purposes.
Analysis and Preliminary Determinations
Negligible Impact
Negligible impact is ``an impact resulting from the specified
activity that cannot be reasonably expected to, and is not reasonably
likely to, adversely affect the species or stock through effects on
annual rates of recruitment or survival'' (50 CFR 216.103). A
negligible impact finding is based on the lack of likely adverse
effects on annual rates of recruitment or survival (i.e., population-
level effects). An estimate of the number of Level B harassment takes,
alone, is not enough information on which to base an impact
determination. In addition to considering estimates of the number of
marine mammals that might be ``taken'' through behavioral harassment,
NMFS must consider other factors, such as the likely nature of any
responses (their intensity, duration, etc.) and the context of any
responses (critical reproductive time or location, migration, etc.), as
well as the number and nature of estimated Level A harassment takes,
the number of estimated mortalities, effects on habitat, and the status
of the species.
In making a negligible impact determination, NMFS evaluated factors
such as:
(1) The number of anticipated serious injuries and or mortalities;
(2) The number and nature of anticipated injuries;
(3) The number, nature, intensity, and duration of takes by Level B
harassment (all of which are relatively limited in this case);
(4) The context in which the takes occur (e.g., impacts to areas of
significance, impacts to local populations, and cumulative impacts when
taking into account successive/contemporaneous actions when added to
baseline data);
[[Page 15093]]
(5) 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);
(6) Impacts on habitat affecting rates of recruitment/survival; and
(7) The effectiveness of monitoring and mitigation measures.
NMFS has preliminarily determined that the specified activities
associated with the marine seismic survey are not likely to cause PTS,
or other (non-auditory) injury, serious injury, or death, based on the
analysis above and the following factors:
(1) The likelihood that, given sufficient notice through relatively
slow ship speed, marine mammals are expected to move away from a noise
source that is annoying prior to its becoming potentially injurious;
(2) The availability of alternate areas of similar habitat value
for marine mammals to temporarily vacate the survey area during the
operation of the airgun(s) to avoid acoustic harassment;
(3) The potential for temporary or permanent hearing impairment is
relatively low and would likely be avoided through the implementation
of the required monitoring and mitigation measures (including shut-down
measures); and
(4) The likelihood that marine mammal detection ability by trained
PSOs is high at close proximity to the vessel.
No injuries, serious injuries, or mortalities are anticipated to
occur as a result of the SIO's planned low-energy seismic survey, and
none are proposed to be authorized by NMFS. Table 5 of this document
outlines the number of requested Level B harassment takes that are
anticipated as a result of these activities. Due to the nature, degree,
and context of Level B (behavioral) harassment anticipated and
described in this notice (see ``Potential Effects on Marine Mammals''
section above), the activity is not expected to impact rates of annual
recruitment or survival for any affected species or stock, particularly
given NMFS's and the applicant's proposed mitigation, monitoring, and
reporting measures to minimize impacts to marine mammals. Additionally,
the low-energy seismic survey 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 hr cycle).
Behavioral reactions to noise exposure (such as disruption of critical
life functions, displacement, or avoidance of important habitat) are
more likely to be significant if they last more than one diel cycle or
recur on subsequent days (Southall et al., 2007). While airgun
operations are anticipated to occur on consecutive days, the estimated
duration of the survey would not last more than a total of
approximately 27 operational days. Additionally, the low-energy 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, so
individual animals likely would only be exposed to and harassed by
sound for less than a day.
As mentioned previously, NMFS estimates that 32 species of marine
mammals under its jurisdiction could be potentially affected by Level B
harassment over the course of the IHA. The population estimates for the
marine mammal species that may be taken by Level B harassment were
provided in Table 3 and 5 of this document. As shown in those tables,
the proposed takes represent small proportions of the overall
populations of these marine mammal species where abundance estimates
are available (i.e., less than 1%).
Of the 32 marine mammal species under NMFS jurisdiction that may or
are known to likely occur in the study area, six are listed as
threatened or endangered under the ESA: Southern right, humpback, sei,
fin, blue, and sperm whales. These species are also considered depleted
under the MMPA. None of the other marine mammal species that may be
taken are listed as depleted under the MMPA. Of the ESA-listed species,
incidental take has been requested to be authorized for six species. As
mitigation to reduce impacts to the affected species or stocks, SIO
would be required to cease airgun operations if any marine mammal
enters designated exclusion zones. No injury, serious injury, or
mortality is expected to occur for any of these species, and due to the
nature, degree, and context of the Level B harassment anticipated, and
the activity is not expected to impact rates of recruitment or survival
for any of these species.
NMFS has preliminarily determined that, provided that the
aforementioned mitigation and monitoring measures are implemented, the
impact of conducting a low-energy marine seismic survey in the
Southwest Pacific Ocean, May to June 2015, 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 behavioral modifications, including temporarily vacating the
area during the operation of the airgun(s), may be made by these
species to avoid the resultant acoustic disturbance, the availability
of alternate areas for species to move to and the short and sporadic
duration of the research activities, have led NMFS to preliminary
determine that the taking by Level B harassment from the specified
activity would have a negligible impact on the affected species in the
specified geographic region. Due to the nature, degree, and context of
Level B (behavioral) harassment anticipated and described (see
``Potential Effects on Marine Mammals'' section above) in this notice,
the proposed activity is not expected to impact rates of annual
recruitment or survival for any affected species or stock, particularly
given the NMFS and applicant's proposal to implement mitigation and
monitoring measures would minimize impacts to marine mammals. 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 proposed monitoring and
mitigation measures, NMFS preliminarily finds that the total marine
mammal take from SIO's proposed low-energy seismic survey would have a
negligible impact on the affected marine mammal species or stocks.
Small Numbers
As mentioned previously, NMFS estimates that 32 species of marine
mammals under its jurisdiction could be potentially affected by Level B
harassment over the course of the IHA. The population estimates for the
marine mammal species that may be taken by Level B harassment were
provided in Tables 3 and 5 of this document.
The estimated numbers of individual cetaceans and pinnipeds that
could be exposed to seismic sounds with received levels greater than or
equal to 160 dB re 1 [mu]Pa (rms) during the proposed low-energy
seismic survey (including a 25% contingency) are in Table 5 of this
document. Of the cetaceans, 2 southern right, 2 pygmy right, 2
humpback, 2 Antarctic minke, 2 minke, 2 Bryde's, 2 sei, 2 fin, 2 blue,
and 10 sperm whales could be taken by Level B harassment during the
proposed low-energy seismic survey, which would represent 0.03,
unknown, 0.1, less than 0.01, less than 0.01, less than 0.01, less than
0.01, less than 0.01, 0.03, and 0.03% of the affected worldwide or
regional populations, respectively. In addition, 5 pygmy sperm, 2
Cuvier's beaked, 3 Shepherd's beaked, 2 southern bottlenose, 2 Andrew's
beaked, 2 Blainville's beaked, 2 Gray's beaked,
[[Page 15094]]
2 Hector's beaked, 2 spade-toothed beaked, and 3 strap-toothed beaked
could be taken be Level B harassment during the proposed low-energy
seismic survey, which would represent unknown, less than 0.01, less
than 0.01, less than 0.01, less than 0.01, less than 0.01, less than
0.01, less than 0.01, less than 0.01, and less than 0.01% of the
affected worldwide or regional populations, respectively. Of the
delphinids, 12 killer whales, 10 false killer whales, 20 long-finned
pilot whales, 20 short-finned pilot whales, 95 bottlenose dolphins, 95
dusky dolphins, 38 Hector's dolphins, 57 hourglass dolphins, 189 short-
beaked common dolphins, and 57 southern right whale dolphins could be
taken by Level B harassment during the proposed low-energy seismic
survey, which would represent 0.02, unknown, 0.01, less than 0.01,
0.02, 0.79, 0.51, 0.04, less than 0.01, and unknown of the affected
worldwide or regional populations, respectively. Of the pinnipeds, 15
New Zealand fur seals and 6 southern elephant seals could be taken by
Level B harassment during the proposed low-energy seismic survey, which
would represent 0.01 and less than 0.01 of the affected worldwide or
regional population, respectively.
No known current worldwide or regional population estimates are
available for 4 species under NMFS's jurisdiction that could
potentially be affected by Level B harassment over the course of the
IHA. These species are the pygmy right, pygmy sperm, and false killer
whales and southern right whale dolphins. Pygmy right whales have a
circumglobal distribution and occur throughout coastal and oceanic
waters in the Southern Hemisphere (between 30 to 55[deg] South)
(Jefferson et al., 2008). Pygmy sperm whales occur in deep waters on
the outer continental shelf and slope in tropical to temperate waters
of the Atlantic, Indian, and Pacific Oceans. False killer whales
generally occur in deep offshore tropical to temperate waters (between
50[deg] North to 50[deg] South) of the Atlantic, Indian, and Pacific
Oceans (Jefferson et al., 2008). Southern right whale dolphins have a
circumpolar distribution and generally occur in deep temperate to sub-
Antarctic waters in the Southern Hemisphere (between 30 to 65[deg]
South) (Jefferson et al., 2008). Based on these distributions and
preferences of these species, NMFS concludes that the requested take of
these species likely represent small numbers relative to the affected
species' overall population sizes.
NMFS makes its small numbers determination based on the numbers of
marine mammals that would be taken relative to the populations of the
affected species or stocks. The proposed take estimates all represent
small numbers relative to the affected species or stock size (i.e., all
are less than 1%), with the exception of the four species (i.e., pygmy
right, pygmy sperm, and false killer whales and southern right whale
dolphins) for which a qualitative rationale was provided.
Endangered Species Act
Of the species of marine mammals that may occur in the proposed
survey area, six are listed as endangered under the ESA: The southern
right, humpback, sei, fin, blue, and sperm whales. Under section 7 of
the ESA, NSF, on behalf of SIO, has initiated formal consultation with
the NMFS, Office of Protected Resources, Endangered Species Act
Interagency Cooperation Division, on this proposed low-energy seismic
survey. NMFS's Office of Protected Resources, Permits and Conservation
Division, has initiated formal consultation under section 7 of the ESA
with NMFS's Office of Protected Resources, Endangered Species Act
Interagency Cooperation Division, to obtain a Biological Opinion
evaluating the effects of issuing the IHA on threatened and endangered
marine mammals and, if appropriate, authorizing incidental take. NMFS
would conclude formal section 7 consultation prior to making a
determination on whether or not to issue the IHA. If the IHA is issued,
in addition to the mitigation and monitoring requirements included in
the IHA, NSF and SIO would be required to comply with the Terms and
Conditions of the Incidental Take Statement corresponding to NMFS's
Biological Opinion issued to both NSF and SIO, and NMFS's Office of
Protected Resources.
National Environmental Policy Act
With SIO's complete IHA application, NSF and SIO provided NMFS a
``Draft Environmental Analysis of a Low-Energy Marine Geophysical
Survey by the R/V Roger Revelle in the Southwest Pacific Ocean, East of
New Zealand, May to June 2015,'' (Draft Environmental Analysis),
prepared by LGL Limited, Environmental Research Associates, on behalf
of NSF and SIO. The Draft Environmental Analysis analyzes the direct,
indirect, and cumulative environmental impacts of the proposed
specified activities on marine mammals, including those listed as
threatened or endangered under the ESA. NMFS, after independently
reviewing and evaluating the document for sufficiency and compliance
with Council on Environmental Quality (CEQ) NEPA regulations and NOAA
Administrative Order 216-6 Sec. 5.09(d), will conduct a separate NEPA
analysis and prepare a ``Draft Environmental Assessment on the Issuance
of an Incidental Harassment Authorization to the Scripps Institution of
Oceanography to Take Marine Mammals by Harassment Incidental to a Low-
Energy Marine Geophysical Survey in the Southwest Pacific Ocean, East
of New Zealand, May to June 2015,'' and decide whether to sign a
Finding of No Significant Impact (FONSI), prior to making a
determination on the issuance of the IHA.
Proposed Authorization
As a result of these preliminary determinations, NMFS proposes to
issue an IHA to SIO for conducting the low-energy seismic survey in the
Southwest Pacific Ocean, East of New Zealand, provided the previously
mentioned mitigation, monitoring, and reporting requirements are
incorporated. This section contains a draft of the IHA itself. The
wording contained in this section is proposed for inclusion in the IHA
(if issued). The proposed IHA language is provided below:
The NMFS hereby authorizes the Scripps Institution of Oceanography,
8602 La Jolla Shores Drive, La Jolla, California 92037, under section
101(a)(5)(D) of the Marine Mammal Protection Act (MMPA) (16 U.S.C.
1371(a)(5)(D)), to harass small numbers of marine mammals incidental to
a low-energy marine geophysical (seismic) survey conducted by the R/V
Roger Revelle (Revelle) in the Southwest Pacific Ocean, East of New
Zealand, May to June 2015:
1. Effective Dates
This Authorization is valid from May 18, 2015 through July 30,
2015.
2. Specified Activity and Geographic Region
This Authorization is valid only for SIO's activities associated
with low-energy seismic survey, bathymetric profile, and heat-flow
probe measurements conducted aboard the Revelle that shall occur in the
following specified geographic area:
(a) In selected regions of the Southwest Pacific Ocean off the east
coast of New Zealand. The survey sites are located in the Exclusive
Economic Zone, outside of territorial waters (located between
approximately 38.5 and 42.5[deg] South, and between 174 and 180[deg]
East). Water depths in the survey area are expected to be approximately
200 to 3,000 m. No airgun operations would occur in shallow (less than
100
[[Page 15095]]
m) water depths. Airgun operations would take approximately 135 hours
in total and 1,250 km, and the remainder of the time would be spent in
transit and collecting heat-flow measurements and sediment core
samples. The low-energy seismic survey would be conducted as specified
in SIO's IHA application and the associated NSF and SIO Environmental
Analysis.
3. This Authorization does not permit incidental takes of marine
mammals in the territorial sea of foreign nations, as the MMPA does not
apply in those waters. The territorial sea extends at the most 22.2
kilometers (km) (12 nautical miles [nmi]) from the baseline of a
coastal State.
4. Species Authorized and Level of Takes
(a) The incidental taking of marine mammals, by Level B harassment
only, is limited to the following species in the waters of the
Southwest Pacific Ocean, East of New Zealand:
(i) Mysticetes--see Table 5 (above) for authorized species and take
numbers.
(ii) Odontocetes--see Table 5 (above) for authorized species and
take numbers.
(iii) Pinnipeds--see Table 5 (above) for authorized species and
take numbers.
(iv) If any marine mammal species are encountered during seismic
activities that are not listed in Table 5 (above) for authorized taking
and are likely to be exposed to sound pressure levels (SPLs) greater
than or equal to 160 dB re 1 [mu]Pa (rms) for seismic airgun
operations, then the SIO must alter speed or course or shut-down the
airguns to prevent take.
(b) The taking by injury (Level A harassment), serious injury, or
death of any of the species listed in Condition 4(a) above or the
taking of any kind of any other species of marine mammal is prohibited
and may result in the modification, suspension, or revocation of this
Authorization.
5. The sources authorized for taking by Level B harassment are
limited to the following acoustic sources, absent an amendment to this
Authorization:
A two Generator Injector (GI) airgun array (each with a discharge
volume of 45 cubic inches [in\3\]) with a total volume of 90 in\3\ (or
smaller).
6. Prohibited Take
The taking of any marine mammal in a manner prohibited under this
Authorization must be reported immediately to the Office of Protected
Resources, National Marine Fisheries Service (NMFS), at 301-427-8401.
7. Mitigation and Monitoring Requirements
The SIO is required to implement the following mitigation and
related monitoring requirements when conducting the specified
activities to achieve the least practicable impact on affected marine
mammal species or stocks:
Protected Species Observers and Visual Monitoring
(a) Utilize at least one NMFS-qualified, vessel-based Protected
Species Observer (PSO) to visually watch for and monitor marine mammals
near the seismic source vessel during daylight airgun operations (from
nautical twilight-dawn to nautical twilight-dusk) and before and during
ramp-ups of airguns day or night. Three PSOs shall be based onboard the
vessel.
(i) The Revelle's vessel crew shall also assist in detecting marine
mammals, when practicable.
(ii) PSOs shall have access to reticle binoculars (7 x 50 Fujinon)
equipped with a built-in daylight compass and range reticles, big-eye
binoculars (25 x 150), optical range finders, and night-vision devices.
(iii) PSO shifts shall last no longer than 4 hours at a time.
(iv) PSO(s) shall also make observations during daylight periods
when the seismic airguns are not operating, when feasible, for
comparison of animal abundance and behavior.
(v) PSO(s) shall conduct monitoring while the airgun array and
streamer(s) are being deployed or recovered from the water.
(b) PSO(s) shall record the following information when a marine
mammal is sighted:
(i) 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 including responses to ramp-up), and
behavioral pace; and
(ii) Time, location, heading, speed, activity of the vessel
(including number of airguns operating and whether in state of ramp-up
or shut-down), Beaufort sea state and wind force, visibility, and sun
glare; and
(iii) The data listed under Condition 7(b)(ii) shall also be
recorded at the start and end of each observation watch and during a
watch whenever there is a change in one or more of the variables.
Buffer and Exclusion Zones
(c) Establish a 160 dB re 1 [mu] Pa (rms) buffer zone, as well as
a180 dB re 1 [mu] Pa (rms) exclusion zone for cetaceans and a 190 dB re
1 [mu] Pa (rms) exclusion zone for pinnipeds before the two GI airgun
array (90 in\3\ total volume) is in operation. See Table 2 (above) for
distances and buffer and exclusion zones.
Visual Monitoring at the Start of the Airgun Operations
(d) Visually observe the entire extent of the exclusion zone (180
dB re 1 [mu] Pa [rms] for cetaceans and 190 dB re 1 [mu] Pa [rms] for
pinnipeds; see Table 2 [above] for distances) using two NMFS-qualified
PSOs, for at least 30 minutes prior to starting the airgun array (day
or night).
(i) If the PSO(s) sees a marine mammal within the exclusion zone,
SIO must delay the seismic survey until the marine mammal(s) has left
the area. If the PSO(s) sees a marine mammal that surfaces, then dives
below the surface, the PSO(s) shall continue to observe the exclusion
zone for 30 minutes, and if the PSO sees no marine mammals during that
time, the PSO should assume that the animal has moved beyond the
exclusion zone.
(ii) If for any reason the entire radius cannot be seen for the
entire 30 minutes (i.e., rough seas, fog, darkness), or if marine
mammals are near, approaching, or in the exclusion zone, the airguns
may not be ramped-up. If one airgun is already running at a source
level of at least 180 dB re 1 [mu] Pa (rms), SIO may start the second
airgun without observing the entire exclusion zone for 30 minutes
prior, provided no marine mammals are known to be near the exclusion
zone (in accordance with Condition 7[e] below).
Ramp-Up Procedures
(e) Implement a ``ramp-up'' procedure, which means starting with a
single GI airgun and adding a second GI airgun after five minutes, when
starting up at the beginning of seismic operations or anytime after the
entire array has been shut-down for more than 15 minutes. During ramp-
up, the two PSOs shall monitor the exclusion zone, and if marine
mammals are sighted, a shut-down shall be implemented as though the
full array (both GI airguns) were operational. Therefore, initiation of
ramp-up procedures from shut-down requires that the two PSOs be able to
view the full exclusion zone as described in Condition 7(d) (above).
Shut-Down Procedures
(f) Shut-down the airgun(s) if a marine mammal is detected within,
approaches, or enters the relevant exclusion zone (as defined in Table
2, above). A shut-down means all operating airguns are shut-down (i.e.,
turned off).
[[Page 15096]]
(g) Following a shut-down, the airgun activity shall not resume
until the PSO(s) has visually observed the marine mammal(s) exiting the
exclusion zone and determined it is not likely to return, or has not
seen the marine mammal within the exclusion zone for 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, dwarf and pygmy sperm, killer, and
beaked whales).
(h) Following a shut-down and subsequent animal departure, airgun
operations may resume, following the ramp-up procedures described in
Condition 7(e).
Speed or Course Alteration
(i) Alter speed or course during seismic operations if a marine
mammal, based on its position and relative motion, appears likely to
enter the relevant exclusion zone. If speed or course alteration is not
safe or practicable, or if after alteration the marine mammal still
appears likely to enter the exclusion zone, further mitigation
measures, such as a shut-down, shall be taken.
Survey Operations During Low-Light Hours
(j) Marine seismic surveying may continue into low-light hours if
such segment(s) of the survey is initiated when the entire relevant
exclusion zones are visible and can be effectively monitored.
(k) No initiation of airgun array operations is permitted from a
shut-down position during low-light hours (such as in dense fog or
heavy rain) when the entire relevant exclusion zone cannot be
effectively monitored by the PSO(s) on duty.
(l) To the maximum extent practicable, schedule seismic operations
(i.e., shooting airguns) during daylight hours, and heat-flow
measurements at nighttime hours.
8. Reporting Requirements
SIO are required to:
(a) Submit a draft report on all activities and monitoring results
to the Office of Protected Resources, NMFS, within 90 days of the
completion of the Revelle's Southwest Pacific Ocean, East of New
Zealand cruise. This report must contain and summarize the following
information:
(i) Dates, times, locations, heading, speed, weather, sea
conditions (including Beaufort sea state and wind force), and
associated activities during all seismic operations and marine mammal
sightings;
(ii) Species, number, location, distance from the vessel, and
behavior of any marine mammals, as well as associated seismic activity
(e.g., number of shut-downs), observed throughout all monitoring
activities.
(iii) An estimate of the number (by species) of marine mammals
that: (A) Are known to have been exposed to the seismic activity (based
on visual observation) at received levels greater than or equal to 160
dB re 1 [mu]Pa (rms) (for seismic airgun operations), and/or 180 dB re
1 [mu]Pa (rms) for cetaceans and 190 dB re 1 [mu]Pa (rms) for
pinnipeds, with a discussion of any specific behaviors those
individuals exhibited; and (B) may have been exposed (based on modeled
values for the two GI airgun array) to the seismic activity at received
levels greater than or equal to 160 dB re 1 [mu]Pa (rms) (for seismic
airgun operations), and/or 180 dB re 1 [mu]Pa (rms) for cetaceans and
190 dB re 1 [mu]Pa (rms) for pinnipeds, with a discussion of the nature
of the probable consequences of that exposure on the individuals that
have been exposed.
(iv) A description of the implementation and effectiveness of the:
(A) Terms and Conditions of the Biological Opinion's Incidental Take
Statement (ITS) (attached); and (B) mitigation measures of the IHA. For
the Biological Opinion, the report shall confirm the implementation of
each Term and Condition, as well as any conservation recommendations,
and describe their effectiveness, for minimizing the adverse effects of
the action on Endangered Species Act-listed marine mammals.
(b) Submit a final report to the Chief, Permits and Conservation
Division, Office of Protected Resources, NMFS, within 30 days after
receiving comments from NMFS on the draft report. If NMFS decides that
the draft report needs no comments, the draft report shall be
considered to be the final report.
8. Reporting Prohibited Take
(a) (i) In the unanticipated event that the specified activity
clearly causes the take of a marine mammal in a manner prohibited by
this Authorization, such as an injury (Level A harassment), serious
injury or mortality (e.g., through ship-strike, gear interaction, and/
or entanglement), SIO shall immediately cease the specified activities
and immediately report the incident to the Chief of the Permits and
Conservation Division, Office of Protected Resources, NMFS, at 301-427-
8401 and/or by email to Jolie.Harrison@noaa.gov and
Howard.Goldstein@noaa.gov. The report must include the following
information:
(ii) Time, date, and location (latitude/longitude) of the incident;
the name and type of vessel involved; the 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 marine mammal
observations in the 24 hours preceding the incident; species
identification or description of the animal(s) involved; the fate of
the animal(s); and photographs or video footage of the animal (if
equipment is available).
Activities shall not resume until NMFS is able to review the
circumstances of the prohibited take. NMFS shall work with SIO to
determine what is necessary to minimize the likelihood of further
prohibited take and ensure MMPA compliance. SIO may not resume their
activities until notified by NMFS via letter, email, or telephone.
Reporting an Injured or Dead Marine Mammal With an Unknown Cause of
Death
(b) In the event that SIO discover an injured or dead marine
mammal, and the lead PSO determines that the cause of the injury or
death is unknown and the death is relatively recent (i.e., in less than
a moderate state of decomposition), SIO shall immediately report the
incident to the Chief of the Permits and Conservation Division, Office
of Protected Resources, NMFS, at 301-427-8401, and/or by email to
Jolie.Harrison@noaa.gov and Howard.Goldstein@noaa.gov. The report must
include the same information identified in Condition 8(c)(i) above.
Activities may continue while NMFS reviews the circumstances of the
incident. NMFS shall work with SIO to determine whether modifications
in the activities are appropriate.
Reporting an Injured or Dead Marine Mammal Not Related to the
Activities
(c) In the event that SIO discovers an injured or dead marine
mammal, and the lead PSO determines that the injury or death is not
associated with or related to the activities authorized in Condition 2
of this Authorization (e.g., previously wounded animal, carcass with
moderate to advanced decomposition, or scavenger damage), SIO shall
report the incident to the Chief of the Permits and Conservation
Division, Office of Protected Resources, NMFS, at 301-427-8401, and/or
by email to Jolie.Harrison@noaa.gov and Howard.Goldstein@noaa.gov,
within 24 hours of the discovery. SIO shall provide photographs or
video footage (if available) or other documentation of the
[[Page 15097]]
stranded animal sighting to NMFS. Activities may continue while NMFS
reviews the circumstances of the incident.
9. Endangered Species Act Biological Opinion and Incidental Take
Statement
(a) SIO is required to comply with the Terms and Conditions of the
ITS corresponding to NMFS's Biological Opinion issued to both NSF and
SIO, and NMFS's Office of Protected Resources.
(b) A copy of this Authorization and the ITS must be in the
possession of all contractors and PSO(s) operating under the authority
of this Incidental Harassment Authorization.
Request for Public Comments
NMFS requests comment on our analysis, the draft authorization, and
any other aspect of the notice of the proposed IHA for SIO's low-energy
seismic survey. Please include with your comments any supporting data
or literature citations to help inform our final decision on SIO's
request for an MMPA authorization. Concurrent with the publication of
this notice in the Federal Register, NMFS is forwarding copies of this
application to the Marine Mammal Commission and its Committee of
Scientific Advisors.
Dated: March 12, 2015.
Perry Gayaldo,
Deputy Director, Office of Protected Resources, National Marine
Fisheries Service.
[FR Doc. 2015-06261 Filed 3-19-15; 8:45 am]
BILLING CODE 3510-22-P