Small Takes of Marine Mammals Incidental to Specified Activities; Low-Energy Marine Seismic Survey in the Northeastern Indian Ocean, May-August 2007, 17849-17864 [E7-6750]
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Federal Register / Vol. 72, No. 68 / Tuesday, April 10, 2007 / Notices
negligible impact on this species. In
addition, NMFS has determined that
bearded and spotted seals, if present
within the vicinity of the project area
could also be taken incidentally, by no
more than Level B harassment and that
such taking would have a negligible
impact on such species or stocks.
Although there is not a specfic number
assessed for the taking of bearded and
spotted seals due to their rare
occurrence in the project area, NMFS
believes that any take would be
significantly lower than those of ringed
seals. NMFS also finds that the action
will not have an unmitigable adverse
impact on the availability of such
species or stocks for taking for
subsistence uses.
In addition, no take by Level A
harassment (injury) or death is
anticipated or authorized, and
harassment takes should be at the
lowest level practicable due to
incorporation of the mitigation
measures described in this document.
Authorization
NMFS has issued an IHA to SOI for
the potential Level B harassment of
small number of ringed seals, and
potential Level B harassment of bearded
and spotted seals incidental to
conducting on-ice seismic R&D program
in the U.S. Beaufort Sea, provided the
previously mentioned mitigation,
monitoring, and reporting requirements
are incorporated.
Dated: March 30, 2007.
Angela Somma,
Acting Director, Office of Protected Resources,
National Marine Fisheries Service.
[FR Doc. E7–6653 Filed 4–9–07; 8:45 am]
BILLING CODE 3510–22–S
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
[I.D. 040307B]
Small Takes of Marine Mammals
Incidental to Specified Activities; LowEnergy Marine Seismic Survey in the
Northeastern Indian Ocean, MayAugust 2007
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; proposed incidental
take authorization; request for
comments.
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AGENCY:
SUMMARY: NMFS has received an
application from Scripps Institute of
Oceanography (SIO) for an Incidental
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Harassment Authorization (IHA) to take
marine mammals incidental to
conducting a low-energy marine seismic
survey in the northeastern Indian Ocean
during May-August 2007. Pursuant to
the Marine Mammal Protection Act
(MMPA), NMFS is requesting comments
on its proposal to issue an IHA to SIO
to incidentally take, by Level B
harassment only, several species of
marine mammals during the
aforementioned activity.
DATES: Comments and information must
be received no later than May 10, 2007.
ADDRESSES: Comments on the
application should be addressed to
Michael Payne, Chief, Permits,
Conservation and Education Division,
Office of Protected Resources, National
Marine Fisheries Service, 1315 EastWest Highway, Silver Spring, MD
20910–3225. The mailbox address for
providing email comments is
PR1.040307B@noaa.gov. NMFS is not
responsible for e-mail comments sent to
addresses other than the one provided
here. Comments sent via e-mail,
including all attachments, must not
exceed a 10–megabyte file size.
A copy of the application containing
a list of the references used in this
document may be obtained by writing to
the address specified above, telephoning
the contact listed below (see FOR
FURTHER INFORMATION CONTACT), or
visiting the internet at: https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm#applications.
Documents cited in this notice may be
viewed, by appointment, during regular
business hours, at the aforementioned
address.
FOR FURTHER INFORMATION CONTACT: Jolie
Harrison, Office of Protected Resources,
NMFS, (301) 713–2289, ext 166.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the
MMPA (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce to allow,
upon request, the incidental, but not
intentional, taking of marine mammals
by U.S. citizens who engage in a
specified activity (other than
commercial fishing) within a specified
geographical region if certain findings
are made and either regulations are
issued or, if the taking is limited to
harassment, a notice of a proposed
authorization is provided to the public
for review.
Authorization 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
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17849
(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. 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].
Section 101(a)(5)(D) establishes a 45–
day time limit for NMFS review of an
application followed by a 30–day public
notice and comment period on any
proposed authorizations for the
incidental harassment of marine
mammals. Within 45 days of the close
of the comment period, NMFS must
either approve or deny the
authorization.
Summary of Request
On January 5, 2007, NMFS received
an application from SIO for the taking,
by Level B harassment only, of 32
species of marine mammals incidental
to conducting, with research funding
from the National Science Foundation
(NSF), a low-energy marine seismic
survey in the northeastern Indian Ocean
from May-August 2007. The purpose of
the research program is to conduct a
scientific rock-dredging, magnetic,
bathymetric, and seismic survey
program at nine sites on the Ninety East
Ridge in the northeastern Indian Ocean.
The results will be used to (1) determine
the morphology, structure, and tectonics
of ridge volcanoes to see whether they
reflect centralized (plume) or
distributed (crack) eruptions; (2) infer
the magmatic evolution of the ridge,
whether it fits the plume hypothesis,
and its connection to existing hotspots;
(3) examine the duration of volcanism at
the various sites and along the ridge to
see whether the age progression fits the
simple plume model; and (4) survey
broad characteristics of subseafloor in
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order to refine the planning of the IODP
drilling proposal. Included in the
research planned for 2007 are scientific
rock dredging at all nine sites, highresolution seismic methods to image the
subsea floor at five of the sites, and the
use of a magnetometer, gravimeter,
multi-beam sonar, and sub-bottom
profiler throughout the cruise.
Description of the Activity
The seismic surveys will involve one
vessel, the R/V Roger Revelle (Roger
Revelle), which is scheduled to depart
from Fremantle, Australia, between May
22 and June 19, 2007. The Roger Revelle
will conduct the cruise in the Indian
Ocean and arrive at Colombo, Sri Lanka,
between July 16 and August 13, 2007.
The exact dates of the activities may
vary by a few days because of weather
conditions, repositioning, streamer
operations and adjustments, airgun
deployment, or the need to repeat some
lines if data quality is substandard.
Additional seismic operations may be
occasionally needed to investigate
significant new findings as revealed by
the other survey systems. The overall
area within which the seismic surveys
will occur is located between
approximately 5° N. and 25° S., along
approximately 90o E. (Figure 1 in the
application), in the Indian Ocean. The
surveys will be conducted entirely in
International Waters.
The Roger Revelle will deploy a pair
of low-energy Generator-Injector (GI)
airguns as an energy source (each with
a discharge volume of 45 in3), plus a
800 m-long (2625–ft long), 48–channel,
towed hydrophone. The program will
consist of approximately 2700 km (1678
mi) of surveys, including turns. Water
depths within the seismic survey areas
are 1600–5100 m (1750–5577 yd). The
GI guns will be operated on a small grid
for approximately 49 hours at each of 5
sites over a approximately 50–day
period during May-August 2007,
commencing between May 22 and June
19. There will be additional seismic
operations associated with equipment
testing, start-up, and repeat coverage of
any areas where initial data quality is
sub-standard.
In addition to the operations of the GI
guns, a 3.5–kHz sub-bottom profiler , a
Kongsberg-Simrad EM–120 multi-beam
sonar, and a gravimeter will be used
continuously throughout the cruise, and
passive geophysical sensors will be
deployed to conduct magnetic surveys
at all times except during dredging.
Vessel Specifications
The Roger Revelle has a length of 83
m (272 ft), a beam of 16 m (52 ft), and
a maximum draft of 5.2 m. The ship is
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powered by two 3,000 hp Propulsion
General Electric motors and an 1180–hp
Azimuthing jet bow thruster. An
operation speed of 11.1 km/h (6 knots)
is used during seismic acquisition.
When not towing seismic survey gear,
the Roger Revelle cruises at 22.2–23.1
km/h (12–12.5 knots) and has a
maximum speed of 27.8 km/h (15
knots). It has a normal operating range
of approximately 27,780 km (17,262 mi).
Acoustic Source Specifications
Seismic Airguns
The vessel Roger Revelle will tow a
pair of GI airguns and an 800 m-long
(2624–ft), 48–channel hydrophone
streamer. Seismic pulses will be emitted
at intervals of 6–10 seconds, which
corresponds to a shot interval of
approximatley 18.5–31 m (61–102 ft) (at
a speed of 6 knots (11.1 km/h). The
generator chamber of each GI gun, the
one responsible for introducing the
sound pulse into the ocean, is 45 in3
(total air discharge approximately 90
in3). The larger (105 in3) injector
chamber injects air into the previouslygenerated bubble to maintain its shape,
and does not introduce more sound into
the water. The two 45 in3 GI guns will
be towed 8 m (26 ft) apart side by side,
21 m (69 ft) behind the Roger Revelle,
at a depth of 2 m (6.6 ft). The dominant
frequency components are 0–188 Hz.
The sound pressure field of that GI
gun variation has not been modeled, but
that for two 45 in3 Nucleus G guns
(which actually have more energy than
GI guns of the same size) has been
modeled by the Lamont-Doherty Earth
Observatory (L-DEO) in relation to
distance and direction from the airguns.
This source, which is directed
downward, was found to have an output
(0–peak) of 230.6 dB re 1 µPa m. The
nominal downward-directed source
levels indicated above 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 from a hypothetical
point source emitting the same total
amount of sound as is emitted by the
combined GI guns. The actual received
level at any location in the water near
the GI guns will not exceed the source
level of the strongest individual source.
In this case, that will be about 224.6 dB
re 1 µPa-m peak, or 229.8 dB re 1 µPam peak-to-peak. Actual levels
experienced by any organism more than
1 m from either GI gun will be
significantly lower.
A further consideration is that the rms
(root mean square) received levels that
are used as impact criteria for marine
mammals are not directly comparable to
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the peak or peak to peak values
normally used to characterize source
levels of airgun arrays. The
measurement units used to describe
airgun sources, peak or peak-to-peak
decibels, are always higher than the
‘‘root mean square’’ (rms) decibels
referred to in biological literature. A
measured received level of 160 dB rms
in the far field would typically
correspond to a peak measurement of
approximately 170 to 172 dB, and to a
peak-to-peak measurement of
approximately 176 to 178 dB, as
measured for the same pulse received at
the same location (Greene 1997;
McCauley et al., 1998, 2000). The
precise difference between rms and
peak or peak-to-peak values depends on
the frequency content and duration of
the pulse, among other factors.
However, the rms level is always lower
than the peak or peak-to-peak level for
an airgun-type source.
Bathymetric Sonar
The Roger Revelle will utilize the
Kongsberg-Simrad EM120 multi-beam
sonar, which operates at 11.25–12.6 kHz
and is mounted in the hull. It operates
in several modes, depending on water
depth. In the proposed survey, it will be
used in deep (>800–m (2625 ft)) water,
and will operate in ‘‘Deep’’ mode. The
beam width is 1° or 2° fore-aft and a
total of 150° athwartship. Estimated
maximum source levels are 239 and 233
dB at 1° and 2° beam widths,
respectively. Each ‘‘ping’’ consists of
nine successive fan-shaped
transmissions, each ensonifying a sector
that extends 1° or 2° fore-aft. In the
‘‘Deep’’ mode, the total duration of the
transmission into each sector is 15 ms.
The nine successive transmissions span
an overall cross-track angular extent of
about 150 degrees, with 16 ms gaps
between the pulses for successive
sectors. A receiver in the overlap area
between two sectors would receive two
15–ms pulses separated by a 16–ms gap.
The ‘‘ping’’ interval varies with water
depth, from approximately 5 s at 1000
m (3280 ft) to 20 s at 4000 m (13120 ft).
Sub-bottom Profiler
The Roger Revelle will utilize the
Knudsen Engineering Model 320BR subbottom profiler, which is a dualfrequency transceiver designed to
operate at 3.5 and/or 12 kHz. It is used
in conjunction with the multi-beam
sonar to provide data about the
sedimentary features that occur below
the sea floor. The energy from the subbottom profiler is directed downward
(in an 80–degree cone) via a 3.5–kHz
transducer array mounted in the hull.
The maximum power output of the
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320BR is 10 kilowatts for the 3.5–kHz
section and 2 kilowatts for the 12–kHz
section. (The 12–kHz section is seldom
used in survey mode on Roger Revelle
because of overlap with the operating
frequency of the Kongsberg Simrad EM–
120 multi-beam sonar.)
The pulse length for the 3.5 kHz
section of the 320BR is 0.8–24 ms,
controlled by the system operator in
regards to water depth and reflectivity
of the bottom sediments, and will
usually be 12 or 24 ms in this survey.
The system produces one sound pulse
and then waits for its return before
transmitting again. Thus, the pulse
interval is directly dependent upon
water depth, and in this survey is 4.5–
8 sec. Using the Sonar Equations and
assuming 100 percent efficiency in the
system (impractical in real world
applications), the source level for the
320BR is calculated to be 211 dB re 1
µPa-m. In practice, the system is rarely
operated above 80 percent power level.
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Safety Radii
NMFS has determined that for
acoustic effects, using acoustic
thresholds in combination with
corresponding safety radii is the most
effective way to consistently apply
measures to avoid or minimize the
impacts of an action, and to
quantitatively estimate the effects of an
action. Thresholds are used in two
ways: (1) to establish a mitigation shutdown or power down zone, i.e., if an
animal enters an area calculated to be
ensonified above the level of an
established threshold, a sound source is
powered down or shut down; and (2) to
calculate take, in that a model may be
used to calculate the area around the
sound source that will be ensonified to
that level or above, then, based on the
estimated density of animals and the
distance that the sound source moves,
NMFS can estimate the number of
marine mammals that may be ‘‘taken’’.
NMFS believes that to avoid permanent
physiological damage (Level A
Harassment), cetaceans and pinnipeds
should not be exposed to pulsed
underwater noise at received levels
exceeding, respectively, 180 and 190 dB
re 1 µPa (rms). NMFS also assumes that
cetaceans or pinnipeds exposed to
levels exceeding 160 dB re 1 µPa (rms)
may experience Level B Harassment.
Received sound levels have been
modeled by L-DEO for a number of
airgun configurations, including two
45–in3 Nucleus G-guns, in relation to
distance and direction from the airguns.
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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 guns where sound
levels of 190, 180, and 160 dB re 1 µPa
(rms) are predicted to be received in
deep (≤1000–m (3280–ft)) water are 10,
40, and 400 m (33, 131, and 1312 ft),
respectively. Because the model results
are for G guns, which have more energy
than GI guns of the same size, those
distances are overestimates of the
distances for the 45–in3 GI guns.
Empirical data concerning the 180and 160- dB distances have been
acquired based on measurements during
the acoustic verification study
conducted by L-DEO in the northern
Gulf of Mexico from 27 May to 3 June
2003 (Tolstoy et al., 2004). Although the
results are limited, the data showed that
radii around the airguns where the
received level would be 180 dB re 1 µPa
(rms) vary with water depth. Similar
depth-related variation is likely in the
190–dB distances applicable to
pinnipeds. Correction factors were
developed for water depths 100–1000 m
(328–3280 ft) and <100 m (328 ft). The
proposed survey will occur in depths
1600–5100 m (5249–16732 ft), so the
correction factors are not relevant here.
The empirical data indicate that, for
deep water (>1000 m (3280 ft)), the LDEO model tends to overestimate the
received sound levels at a given
distance (Tolstoy et al., 2004). However,
to be precautionary pending acquisition
of additional empirical data, it is
proposed that safety radii during airgun
operations in deep water will be the
values predicted by L-DEO’s model
(above). Therefore, the assumed 180and 190–dB radii are 40 m and 10 m
(131 and 33 ft), respectively.
Airguns will be shut down
immediately when cetaceans or
pinnipeds are detected within or about
to enter the appropriate 180–dB (rms) or
190–dB (rms) radius, respectively.
Description of Marine Mammals in the
Activity Area
Thirty-two species of cetacean,
including 25 odontocete (dolphins and
small and large toothed whales) species
and seven mysticete (baleen whales)
species, are thought to occur in the
proposed seismic survey areas along the
Ninety East Ridge in the northeastern
Indian Ocean (Table 1). Several are
listed under the U.S. Endangered
Species Act (ESA) as Endangered: the
sperm whale, humpback whale, blue
whale, fin whale, and sei whale.
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Although there have been several
surveys of marine mammals in the
Indian Ocean (e.g., Keller et al., 1982;
Leatherwood et al., 1984; Eyre 1995;
Baldwin et al., 1998; de Boer 2000; de
Boer et al., 2003), data on the
occurrence, distribution, and abundance
of odontocetes and mysticetes in the
northeastern Indian Ocean,
encompassing the proposed seismic
survey area along the Ninety East Ridge,
are limited or lacking. Commercial
whaling severely depleted all the large
whale populations in this region, and
subsequently, in 1979, the International
Whaling Commission declared the
Indian Ocean north of 55° S. latitude a
whale sanctuary. The majority of recent
detailed information on whales within
the Indian Ocean Sanctuary (IOS) comes
from
(1) A United Nations Environment
Programme (UNEP) Report summarizing
cetacean research in the western IOS
(Leatherwood and Donovan 1991);
(2) A compilation of sightings for the
entire IOS produced by the Whale and
Dolphin Conservation Society (de Boer
et al., 2003); and
(3) A review of marine mammals
records in India (Sathasivam 2004); and
(4) A series of research cruises within
the IOS (Keller et al., 1982;
Leatherwood et al., 1984; Corbett 1994;
Eyre 1995; Ballance and Pitman 1998;
de Boer 2000).
Because the proposed survey area
spans such a wide range of latitudes
(approximately 5° N.-25° S.), tropical
and temperate species are found there.
The survey area is all in deep-water
habitat but is close to oceanic island
habitats (i.e., Andaman, Nicobar, and
Cocos (Keeling) Islands), so both coastal
and oceanic species might be
encountered, although species that stay
in very shallow water (e.g., Indian
hump-backed dolphin, Irrawaddy
dolphin, and finless porpoise) would
not. Abundance and density estimates
of cetaceans found in areas other than
the northeastern and central Indian
Ocean are provided for reference only,
and are not necessarily the same as
those in the survey area. Table 1 also
shows the estimated abundance of the
marine mammals likely to be
encountered during the Roger Revelle’s
cruise. Additional information regarding
the distribution of these species and
how the estimated densities were
calculated may be found in SIO’s
application.
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Species
Habitat
Occurrence
Rqstd Take
Mainly nearshore waters and banks
Common
5(0)**
Minke whale (Balaenoptera acutorostrata)
Pelagic and coastal
Uncommon
5
Antarctic minke
bonaerensis)
Coastal and oceanic
Uncommon
5
Bryde’s whale (Balaenoptera edeni)
Pelagic and coastal
Very common
5
Sei whale (Balaenoptera borealis) *
Primarily offshore, pelagic
Uncommon
5(0)**
Fin whale (Balaenoptera physalus)*
Continental slope, mostly pelagic
Common
5(0)**
Pelagic and coastal
Very common
5(1)**
Usually pelagic and deep seas
Common
5(1)**
Pygmy sperm whale (Kogia breviceps)
Deep waters off the shelf
Common
5
Dwarf sperm whale (Kogia sima)
Deep waters off the shelf
Common
5
Cuvier’s beaked whale (Ziphius cavirostris)
Pelagic
Common
5
Shepherd’s beaked
shepherdi))
whale
(Tasmacetus
Pelagic
Rare
5
Longman’s beaked
pacificus)
whale
(Indopacetus
Pelagic
Common?
1
Southern bottlenose whale (Hyperoodon
planifrons)
Pelagic
Uncommon
5
True’s beaked whale (Mesoplodon mirus)
Pelagic
Rare
5
Gray’s beaked whale (Mesoplodon grayi)
Pelagic
Uncommon
5
Ginkgo-toothed
ginkgodens)
(Mesoplodon
Pelagic
Common
5
(Mesoplodon
Pelagic
Very common
5
Deep water
Uncommon
69
Coastal and oceanic, shelf break
Common
129
Coastal and pelagic
Uncommon
65
Spinner dolphin (Stenella longirostris)
Coastal and pelagic
Abundant
215
Striped dolphin (Stenella coeruleoalba)
Off continental shelf
Common
86
Fraser’s dolphin (Lagenodelphis hosei)
Waters >1000 m
Rare
22
Common dolphin (Delphinus delphis)
Shelf and pelagic, seamounts
Very common
151
Risso’s dolphin (Grampus griseus)
Waters >1000 m, seamounts
Very common
151
Oceanic
Very common
50
Deep, pantropical waters
Common
25
Pelagic
Common
15
Widely distributed
Common
5
Mostly pelagic
Rare
30
Mysticetes
Humpback
whale
novaeangliae)*
(Megaptera
whale
(Balaenoptera
Blue whale (Balaenoptera musculus)*
Odontocetes
Sperm whale (Physeter macrocephalus)*
whale
Blainville’s beaked
densirostris)
whale
Rough-toothed dolphin (Steno bredanensis)
Bottlenose dolphin (Tursiops truncatus)
Pantropical spotted
attenuata)
Melon-headed
electra)
dolphin
whale
(Stenella
(Peponocephala
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Pygmy killer whale (Feresa attenuata)
False killer whale (Pseudorca crassidens)
Killer whale (Orcinus orca)
Long-finned
melas)
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Species
Short-finned pilot
macrorhynchus)
whale
Habitat
(Globicephala
Occurrence
Rqstd Take
Mostly pelagic, high-relief topography
Very common
15
Table 1. Species expected to be encountered (and potentially harassed) during SIO’s Indian Ocean cruise
*Species are listed as endangered under the Endangered Species Act
**Parenthetical numbers represent numbers of takes NMFS proposes to authorize (we may not authorize take ofspecies, or take of numbers of
species, that we are not exempted pursuant to our internal ESA consultation)
Potential Effects on Marine Mammals
Potential Effects of Airguns
The effects of sounds from airguns
might include one or more of the
following: tolerance, masking of natural
sounds, behavioral disturbance, and
temporary or permanent hearing
impairment (Richardson et al., 1995).
Given the small size of the GI guns
planned for the present project, effects
are anticipated to be considerably less
than would be the case with a large
array of airguns. It is very unlikely that
there would be any cases of temporary
or, especially, permanent hearing
impairment. Also, behavioral
disturbance is expected to be limited to
relatively short distances.
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Tolerance
Numerous studies have shown that
pulsed sounds from airguns are often
readily detectable in the water at
distances of many kilometers. For a
summary of the characteristics of airgun
pulses, see Appendix A of SIO’s
application. However, it should be
noted that most of the measurements of
airgun sounds that have been reported
concerned sounds from larger arrays of
airguns, whose sounds would be
detectable considerably farther away
than the GI guns planned for use in the
present project.
Numerous studies have shown that
marine mammals at distances more than
a few kilometers from operating seismic
vessels often show no apparent
response-see Appendix A (e) of SIO’s
application. That is often true even in
cases when the pulsed sounds must be
readily audible to the animals based on
measured received levels and the
hearing sensitivity of that mammal
group. Although various baleen whales,
toothed whales, and (less frequently)
pinnipeds have been shown to react
behaviorally to airgun pulses under
some conditions, at other times
mammals of all three types have shown
no overt reactions. In general, pinnipeds
and small odontocetes seem to be more
tolerant of exposure to airgun pulses
than are baleen whales. Given the
relatively small and low-energy airgun
source planned for use in this project,
mammals (and sea turtles) are expected
to tolerate being closer to this source
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than might be the case for a larger
airgun source typical of most seismic
surveys.
Masking
Masking effects of pulsed sounds
(even from large arrays of airguns) on
marine mammal calls and other natural
sounds are expected to be limited,
although there are very few specific data
on this. Some whales are known to
continue calling in the presence of
seismic pulses. Their calls can be heard
between the seismic pulses (e.g.,
Richardson et al., 1986; McDonald et al.,
1995; Greene et al., 1999; Nieukirk et
al., 2004). Although there has been one
report that sperm whales cease calling
when exposed to pulses from a very
distant seismic ship (Bowles et al.,
1994), a recent study reports that sperm
whales off northern Norway continued
calling in the presence of seismic pulses
(Madsen et al., 2002c). That has also
been shown during recent work in the
Gulf of Mexico (Tyack et al., 2003).
Given the small source planned for use
here, there is even less potential for
masking of baleen or sperm whale calls
during the present study than in most
seismic surveys. Masking effects of
seismic pulses are expected to be
negligible in the case of the smaller
odontocete cetaceans, given the
intermittent nature of seismic pulses
and the relatively low source level of
the airguns to be used here. Also, the
sounds important to small odontocetes
are predominantly at much higher
frequencies than are airgun sounds.
Masking effects, in general, are
discussed further in Appendix A (d) of
SIO’s application.
Disturbance Reactions
Disturbance includes a variety of
effects, including subtle changes in
behavior, more conspicuous changes in
activities, and displacement.
Disturbance is one of the main concerns
in this project. Reactions to sound, if
any, depend on species, state of
maturity, experience, current activity,
reproductive state, time of day, and
many other factors. If a marine mammal
responds to an underwater sound by
changing its behavior or moving a small
distance, the response may or may not
rise to the level of harassment, let alone
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affect the stock or the species as a
whole. Alternatively, if a sound source
displaces marine mammals from an
important feeding or breeding area,
effects on the stock or species could
potentially be more than negligible.
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 are likely to be present
within a particular distance of industrial
activities, or exposed to a particular
level of industrial sound. This practice
potentially overestimates the numbers
of marine mammals that are affected in
some biologically important manner.
The sound criteria used to estimate
how many marine mammals might be
disturbed to some biologicallyimportant degree by a seismic program
are based on behavioral observations
during studies of several species.
However, information is lacking for
many species. Detailed studies have
been done on humpback, gray, and
bowhead whales, and on ringed seals.
Less detailed data are available for some
other species of baleen whales, sperm
whales, and small toothed whales. Most
of those studies have focused on the
impacts resulting from the use of much
larger airgun sources than those planned
for use in the present project. Thus,
effects are expected to be limited to
considerably smaller distances and
shorter periods of exposure in the
present project than in most of the
previous work concerning marine
mammal reactions to airguns.
Baleen Whales – Baleen whales
generally tend to avoid operating
airguns, but avoidance radii are quite
variable. Whales are often reported to
show no overt reactions to pulses from
large arrays of airguns at distances
beyond a few kilometers, even though
the airgun pulses remain well above
ambient noise levels out to much longer
distances. However, as reviewed in
Appendix A (e) of SIO’s application,
baleen whales exposed to strong noise
pulses from airguns often react by
deviating from their normal migration
route and/or interrupting their feeding
activities and moving away from the
sound source. In the case of the
migrating gray and bowhead whales, the
observed changes in behavior appeared
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to be of little or no biological
consequence to the animals. They
simply avoided the sound source by
displacing their migration route to
varying degrees, but within the natural
boundaries of the migration corridors.
Studies of gray, bowhead, and
humpback whales have determined that
received levels of pulses in the 160–170
dB re 1 µPa rms range seem to cause
obvious avoidance behavior in a
substantial fraction of the animals
exposed. In many areas, seismic pulses
from large arrays of airguns diminish to
those levels at distances ranging from
4.5–14.5 km (2.8–9 mi) from the source.
A substantial proportion of the baleen
whales within those distances may
show avoidance or other strong
disturbance reactions to the airgun
array. Subtle behavioral changes
sometimes become evident at somewhat
lower received levels, and recent
studies, reviewed in Appendix A (e) of
SIO’s application, have shown that
some species of baleen whales, notably
bowheads and humpbacks, at times
show strong avoidance at received
levels lower than 160–170 dB re 1 µPa
rms. Reaction distances would be
considerably smaller during the present
project, in which the 160–dB radius is
predicted to be approximately 0.40 km
(0.9 mi), as compared with several
kilometers when a large array of airguns
is operating.
Humpback whales summering in
southeast Alaska did not exhibit
persistent avoidance when exposed to
seismic pulses from a 1.64–L (100 in3)
airgun (Malme et al., 1985). Some
humpbacks seemed ‘‘startled’’ at
received levels of 150–169 dB re 1 µPa
on an approximate rms basis. Malme et
al. (1985) concluded that there was no
clear evidence of avoidance, despite the
possibility of subtle effects, at received
levels up to 172 re 1 µPa (approximately
rms). More detailed information on
responses of humpback whales to
seismic pulses during studies in
Australia can be found in Appendix A
(a) of SIO’s application.
Malme et al. (1986, 1988) studied the
responses of feeding eastern 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 ceased feeding at an
average received pressure level of 173
dB re 1 µPa on an (approximate) rms
basis, and that 10 percent of feeding
whales interrupted feeding at received
levels of 163 dB. Those findings were
generally consistent with the results of
experiments conducted on larger
numbers of gray whales that were
migrating along the California coast.
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Data on short-term reactions (or lack
of reactions) of cetaceans to impulsive
noises do not necessarily provide
information about long-term effects. It is
not known whether impulsive noises
affect reproductive rate or distribution
and habitat use in subsequent days or
years. However, gray whales continued
to migrate annually along the west coast
of North America despite intermittent
seismic exploration and much ship
traffic in that area for decades
(Appendix A in Malme et al., 1984).
Bowhead whales continued to travel to
the eastern Beaufort Sea each summer
despite seismic exploration in their
summer and autumn range for many
years (Richardson et al., 1987). In any
event, the brief exposures to sound
pulses from the present small airgun
source are highly unlikely to result in
prolonged effects.
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, systematic
work on sperm whales is underway
(Tyack et al., 2003).
Seismic operators sometimes see
dolphins and other small toothed
whales near operating airgun arrays, but
in general there seems to be a tendency
for most delphinids to show some
limited avoidance of seismic vessels
operating large airgun systems.
However, some dolphins seem to be
attracted to the seismic vessel and
floats, and some ride the bow wave of
the seismic vessel even when large
arrays of airguns are firing. Nonetheless,
there have been indications that small
toothed whales sometimes 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., Goold, 1996;
Calambokidis and Osmek, 1998; Stone,
2003). Similarly, captive bottlenose
dolphins and beluga whales exhibit
changes in behavior when exposed to
strong pulsed sounds similar in
duration to those typically used in
seismic surveys (Finneran et al., 2000,
2002). However, the animals tolerated
high received levels of sound (pk-pk
level >200 dB re 1 µPa) before exhibiting
aversive behaviors. With the presentlyplanned small airgun system, such
levels would only be found within a few
meters of the airguns.
There are no specific data on the
behavioral reactions of beaked whales to
seismic surveys. A few beaked whale
sightings have been reported from
seismic vessels (Stone, 2003), however,
based on limited observations most
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beaked whales tend to avoid
approaching vessels of other types (e.g.,
Kasuya, 1986; Wursig et al., 1998).
Several beaked whale strandings have
been associated with naval midfrequency sonar exercises, however, the
sounds produced by seismic airguns are
quite different from tactical sonar (see
Appendix A (g) of SIO’s application).
The strandings mentioned above are
apparently at least in part a disturbance
response, although auditory or other
injuries may also be a factor. Whether
beaked whales would ever react
similarly to seismic surveys is unknown
(see ‘‘Strandings and Mortality’’, below).
Sperm whales have been reported to
show avoidance reactions to standard
vessels not emitting airgun sounds, and
it is to be expected that they would tend
to avoid an operating seismic survey
vessel. There were some limited early
observations suggesting that sperm
whales in the Southern Ocean and Gulf
of Mexico might be fairly sensitive to
airgun sounds from distant seismic
surveys. However, more extensive data
from recent studies in the North
Atlantic suggest that sperm whales in
those areas show little evidence of
avoidance or behavioral disruption in
the presence of operating seismic
vessels (McCall Howard, 1999; Madsen
et al., 2002c; Stone, 2003).
Odontocete reactions to large arrays of
airguns are variable and, at least for
small odontocetes, seem to be confined
to a smaller radius than has been
observed for mysticetes. Thus,
behavioral reactions of odontocetes to
the small airgun source to be used here
are expected to be very localized,
probably to distances <0.40 km (.25 mi).
Pinnipeds – Pinnipeds are not likely
to show a strong avoidance reaction to
the small airgun source that will be
used. Visual monitoring from seismic
vessels, usually employing larger
sources, has shown only slight (if any)
avoidance of airguns by pinnipeds, and
only slight (if any) changes in behaviorsee Appendix A (e) of SIO’s application.
Those studies show that pinnipeds
frequently do not avoid the area within
a few hundred meters of operating
airgun arrays, even for arrays much
larger than the one to be used here (e.g.,
Harris et al., 2001). However, initial
telemetry work suggests that avoidance
and other behavioral reactions to small
airgun sources may be stronger than
evident to date from visual studies of
pinniped reactions to airguns
(Thompson et al., 1998). Even if
reactions of the species occurring in the
present study area are as strong as those
evident in the telemetry study, reactions
are expected to be confined to relatively
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small distances and durations, with no
long-term effects on pinnipeds.
Additional details on the behavioral
reactions (or the lack thereof) by all
types of marine mammals to seismic
vessels can be found in Appendix A (e)
of SIO’s application.
Hearing Impairment and Other Physical
Effects
Temporary or permanent hearing
impairment is a possibility when marine
mammals are exposed to very strong
sounds, but there has been no specific
documentation of this for marine
mammals exposed to sequences of
airgun pulses. Current NMFS policy
regarding exposure of marine mammals
to high-level sounds is that cetaceans
and pinnipeds should not be exposed to
impulsive sounds of 180 and 190 dB re
1 µPa (rms), respectively. Those criteria
have been used in defining the safety
(shut-down) radii planned for the
proposed seismic survey. The
precautionary nature of these criteria is
discussed in Appendix A (f) of SIO’s
application, including the fact that the
minimum sound level necessary to
cause permanent hearing impairment is
higher, by a variable and generally
unknown amount, than the level that
induces barely-detectable temporary
threshold shift (TTS) (which NMFS’
criteria are based on) and the level
associated with the onset of TTS is often
considered to be a level below which
there is no danger of permanent damage.
NMFS is presently developing new
noise exposure criteria for marine
mammals that take account of the nowavailable data on TTS in marine (and
terrestrial) mammals.
Because of the small size of the airgun
source in this project (two 45–in3 GI
guns), along with the planned
monitoring and mitigation measures,
there is little likelihood that any marine
mammals will be exposed to sounds
sufficiently strong to cause hearing
impairment. Several aspects of the
planned monitoring and mitigation
measures for this project are designed to
detect marine mammals occurring near
the two GI airguns (and multi-beam
bathymetric sonar), and to avoid
exposing them to sound pulses that
might, at least in theory, cause hearing
impairment. In addition, many
cetaceans are likely to show some
avoidance of the area with high received
levels of airgun sound (see above). In
those cases, the avoidance responses of
the animals themselves will reduce or
(most likely) avoid any possibility of
hearing impairment.
Non-auditory physical effects may
also occur in marine mammals exposed
to strong underwater pulsed sound.
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Possible types of non-auditory
physiological effects or injuries that
theoretically might occur in mammals
close to a strong sound source include
stress, neurological effects, bubble
formation, resonance effects, and other
types of organ or tissue damage. It is
possible that some marine mammal
species (i.e., beaked whales) may be
especially susceptible to injury and/or
stranding when exposed to strong
pulsed sounds. However, as discussed
below, there is no definitive evidence
that any of these effects occur even for
marine mammals in close proximity to
large arrays of airguns. It is especially
unlikely that any effects of these types
would occur during the present project
given the small size of the source, the
brief duration of exposure of any given
mammal, and the planned monitoring
and mitigation measures (see below).
The following subsections discuss in
somewhat more detail the possibilities
of TTS, permanent threshold shift
(PTS), and non-auditory physical
effects.
Temporary Threshold Shift (TTS) –
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.
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
recovers rapidly after exposure to the
noise ends. Only a 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.
For toothed whales exposed to single
short pulses, the TTS threshold appears
to be, to a first approximation, a
function of the energy content of the
pulse (Finneran et al., 2002). Given the
available data, the received level of a
single seismic pulse might need to be
approximately 210 dB re 1 µPa rms
(approximately 221–226 dB pk-pk) in
order to produce brief, mild TTS.
Exposure to several seismic pulses at
received levels near 200–205 dB (rms)
might result in slight TTS in a small
odontocete, assuming the TTS threshold
is (to a first approximation) a function
of the total received pulse energy.
Seismic pulses with received levels of
200–205 dB or more are usually
restricted to a radius of no more than
100 m (328 ft) around a seismic vessel
operating a large array of airguns. Such
levels would be limited to distances
within a few meters of the small GI-gun
source to be used in this project.
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For baleen whales, there are no data,
direct or indirect, on levels or properties
of sound that are required to induce
TTS. However, no cases of TTS are
expected given the small size of the
source, and, as mentioned previously,
there is a strong likelihood that baleen
whales would avoid the approaching GI
gun (or vessel), with the sound source
operating, before being exposed to levels
high enough for there to be any
possibility of TTS.
In pinnipeds, TTS thresholds
associated with exposure to brief pulses
(single or multiple) of underwater sound
have not been measured. Initial
evidence from prolonged exposures
suggested that some pinnipeds may
incur TTS at somewhat lower received
levels than do small odontocetes
exposed for similar durations (Kastak et
al., 1999; Ketten et al., 2001; cf. Au et
al., 2000). However, more recent
indications are that TTS onset in the
most sensitive pinniped species studied
(harbor seal) may occur at a similar
sound exposure level as in odontocetes
(Kastak et al., 2004).
A marine mammal within a radius of
100 m (328 ft) around a typical large
array of operating airguns might be
exposed to a few seismic pulses with
levels of 205 dB, and possibly more
pulses if the mammal moved with the
seismic vessel. (As noted above, most
cetacean species tend to avoid operating
airguns, although not all individuals do
so.) In addition, ramping up airgun
arrays, which is standard operational
protocol for large airgun arrays,
provides an opportunity for cetaceans to
move away from the seismic source and
to avoid being exposed to the full
acoustic output of the airgun array.
However, several of the considerations
that are relevant in assessing the impact
of typical seismic surveys with arrays of
airguns are not directly applicable here:
(1) The planned GI gun source is
much smaller, with correspondingly
smaller radii within which received
sound levels could exceed any
particular level of concern.
(2) With a large airgun array, it is
unlikely that cetaceans would be
exposed to airgun pulses at a
sufficiently high level for a sufficiently
long period to cause more than mild
TTS, given the relative movement of the
vessel and the marine mammal. In this
project, the gun source is much smaller,
so the radius of influence and duration
of exposure to strong pulses is much
smaller, especially in deep and
intermediate-depth water.
(3) With a large array of airguns, TTS
would be most likely in any odontocetes
that bow-ride or otherwise linger near
the airguns. In the present project, the
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anticipated 180–dB distance in deep
water is 40 m (131 ft), and the waterline
at the bow of the Roger Revelle will be
approximately 97 m (318 ft) ahead of the
GI gun.
To avoid injury, NMFS has
determined that cetaceans and
pinnipeds should not be exposed to
pulsed underwater noise at received
levels exceeding, respectively, 180 and
190 dB re 1 µPa (rms). The predicted
180- and 190–dB distances for the GI
guns operated by SIO are 40 m (131 ft)
and 10 m (33 ft), respectively, in water
depths >1000 m (3280 ft). [Those
distances actually apply to operations
with two 45–in3 G guns, and smaller
distances would be expected for the two
45–in3 GI guns to be used here.] These
sound levels are the received levels
above which, in the view of a panel of
bioacoustics specialists convened by
NMFS, one cannot be certain that there
will be no injurious effects, auditory or
otherwise, to marine mammals. More
recent TTS data imply that, at least for
dolphins, TTS is unlikely to occur
unless the dolphins are exposed to
airgun pulses notably stronger than 180
dB re 1 µPa rms. However NMFS
utilizes a precautionary approach of
requiring shut down at received levels
above which we cannot be certain there
will be no injurious effects to the most
sensitive species.
Permanent Threshold Shift (PTS) –
When PTS occurs, there is physical
damage to the sound receptors in the
ear. In some cases, there can be total or
partial deafness, while in other cases,
the animal has an impaired ability to
hear sounds in specific frequency
ranges. 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 TTS, there has been further
speculation about the possibility that
some individuals occurring very close to
airguns might incur PTS. Single or
occasional occurrences of mild TTS are
not indicative of permanent auditory
damage in terrestrial mammals.
Relationships between TTS and PTS
thresholds have not been studied in
marine mammals, but are assumed to be
similar to those in humans and other
terrestrial mammals. PTS might occur at
a received sound level 20 dB or more
above that inducing mild TTS if the
animal were exposed to the strong
sound for an extended period, or to a
strong sound with rather rapid rise timesee Appendix A (f) of SIO’s application.
It is highly unlikely that marine
mammals could receive sounds strong
enough to cause permanent hearing
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impairment during a project employing
two 45–in3 GI guns. In the present
project, marine mammals are unlikely to
be exposed to received levels of seismic
pulses strong enough to cause TTS, as
they would probably need to be within
a few meters of the airguns for that to
occur. Given the higher level of sound
necessary to cause PTS, it is even less
likely that PTS could occur. In fact,
even the levels immediately adjacent to
the airguns may not be sufficient to
induce PTS, especially since a mammal
would not be exposed to more than one
strong pulse unless it swam
immediately alongside an airgun for a
period longer than the inter-pulse
interval (6–10 s). Baleen whales
generally avoid the immediate area
around operating seismic vessels. The
planned monitoring and mitigation
measures, including visual monitoring,
ramp ups, and shut downs of the
airguns when mammals are seen within
the ‘‘safety radii’’, will minimize the
already-minimal probability of exposure
of marine mammals to sounds strong
enough to induce PTS.
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 effects, and other types of
organ or tissue damage. There is no
evidence that any of these effects occur
in marine mammals exposed to sound
from airgun arrays (even large ones) and
there have been no direct studies of the
potential for airgun pulses to elicit any
of those effects. NMFS does not
anticipate that marine mammals would
experience any of these effects in
response to being exposed to the airguns
in this proposed study, especially
considering the small size of the
airguns. If any such effects do occur,
they would probably be limited to
unusual situations when animals might
be exposed at close range for unusually
long periods.
Exposure of laboratory animals,
wildlife, and humans to strong noise
often results in significant increases in
adrenal activity, including cortisol and/
or catecholamine release and related
measures of stress (see Appendix A of
SIO’s application). However, it is
doubtful that any single marine
mammal would be exposed to strong
seismic sounds for sufficiently long that
significant physiological stress would
develop. That is especially so in the
case of the present project where the
airguns are small, the ship’s speed is
relatively fast (5–8 knots or 9.3–14.8
km/h), and each survey does not
encompass a large area.
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Gas-filled structures in marine
animals have an inherent fundamental
resonance frequency. If stimulated at
that frequency, the ensuing resonance
could cause damage to the animal. A
workshop (Gentry [ed.] 2002) was held
to discuss whether the stranding of
beaked whales in the Bahamas in 2000
(Balcomb and Claridge, 2001; NOAA
and USN, 2001) might have been related
to air cavity resonance or bubble
formation in tissues caused by exposure
to noise from naval sonar. A panel of
experts concluded that resonance in airfilled structures was not likely to have
caused this stranding. Opinions were
less conclusive about the possible role
of gas (nitrogen) bubble formation/
growth in the Bahamas stranding of
beaked whales.
Until recently, it was assumed that
diving marine mammals are not subject
to the bends or air embolism. However,
a short paper concerning beaked whales
stranded in the Canary Islands in 2002
suggests that cetaceans might be subject
to decompression injury in some
situations (Jepson et al., 2003). If so, that
might occur if they ascend quickly
when exposed to aversive sounds.
However, the interpretation that the
effect was related to decompression
injury is unproven (Piantadosi and
Thalmann 2004; Fernandez et al., 2004).
Even if that effect can occur during
exposure to mid-frequency sonar, there
is no evidence that this type of effect
occurs in response to airgun sounds. It
is especially unlikely in the case of the
proposed survey, involving only two GI
guns.
In general, little is known about the
potential for seismic survey sounds to
cause auditory impairment or other
physical effects in marine mammals.
Available data suggest that such effects,
if they occur at all, would be limited to
short distances and probably to projects
involving large arrays of airguns.
However, the available data do not
allow for 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 auditory
impairment or other physical effects.
Also, the planned mitigation measures,
including ramp ups and shut downs,
will reduce any such effects that might
otherwise occur.
Strandings and Mortality
Marine mammals close to underwater
detonations of high explosives can be
killed or severely injured, and their
auditory organs are especially
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susceptible to injury (Ketten et al., 1993;
Ketten 1995). Airgun pulses are less
energetic and have slower rise times,
and there is no proof that they can cause
serious injury, death, or stranding even
in the case of large airgun arrays.
However, the association of several
strandings of beaked whales with naval
exercises and, in one case, an L-DEO
seismic survey, has raised the
possibility that beaked whales exposed
to strong pulsed sounds may be
especially susceptible to injury and/or
behavioral reactions that can lead to
stranding. Appendix A (g) of SIO’s
application provides additional details.
Seismic pulses and mid-frequency
sonar pulses are quite different. Sounds
produced by airgun arrays are
broadband with most of the energy
below 1 kHz. Typical military midfrequency sonars operate at frequencies
of 2–10 kHz, generally with a relatively
narrow bandwidth at any one time.
Thus, it is not appropriate to assume
that there is a direct connection between
the effects of military sonar and seismic
surveys on marine mammals. However,
evidence that sonar pulses can, in
special circumstances, lead to physical
damage and mortality (NOAA and USN
2001; Jepson et al., 2003), even if only
indirectly, suggests that caution is
warranted when dealing with exposure
of marine mammals to any highintensity pulsed sound.
In May 1996, 12 Cuvier’s beaked
whales stranded along the coasts of
Kyparissiakos Gulf in the Mediterranean
Sea. That stranding was subsequently
linked to the use of low- and mediumfrequency active sonar by a North
Atlantic Treaty Organization (NATO)
research vessel in the region (Frantzis
1998). In March 2000, a population of
Cuvier’s beaked whales being studied in
the Bahamas disappeared after a U.S.
Navy task force using mid-frequency
tactical sonars passed through the area;
some beaked whales stranded (Balcomb
and Claridge, 2001; NOAA and USN,
2001).
In September 2002, a total of 14
beaked whales of various species
stranded coincident with naval
exercises in the Canary Islands (Martel
n.d.; Jepson et al., 2003; Fernandez et
al., 2003). Also in Sept. 2002, there was
a stranding of two Cuvier’s beaked
whales in the Gulf of California, Mexico,
when the L-DEO vessel Maurice Ewing
was operating a 20–gun, 8490–in3 array
in the general area. The link between
the stranding and the seismic surveys
was inconclusive and not based on any
physical evidence (Hogarth, 2002;
Yoder, 2002). Nonetheless, that plus the
incidents involving beaked whale
strandings near naval exercises suggests
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a need for caution in conducting seismic
surveys in areas occupied by beaked
whales.
The present project will involve a
much smaller sound source than used in
typical seismic surveys. That, along
with the monitoring and mitigation
measures that are planned, are expected
to minimize any possibility for
strandings and mortality.
Potential Effects of Other Acoustic
Devices
Bathymetric Sonar Signals
A multi-beam bathymetric sonar
(Simrad EM120, 11.25–12.6 kHz) will be
operated from the source vessel during
much of the planned study. Sounds
from the multi-beam sonar are very
short pulses. Most of the energy in the
sound pulses emitted by the multi-beam
is at moderately high frequencies,
centered at 12 kHz. The beam is narrow
(1° or 2°) in fore-aft extent, and wide
(150°) in the cross-track extent. Each
ping consists of nine successive
transmissions (segments) at different
cross-track angles. Any given mammal
at depth near the track line would be in
the main beam for only a fraction of a
second.
Tactical Navy sonars that have been
linked to avoidance reactions and
stranding of cetaceans (1) generally are
more powerful than the Simrad EM120,
(2) have a longer pulse duration, and (3)
are directed close to omnidirectionally,
vs. downward for the Simrad EM120.
The area of possible influence of the
Simrad EM120 is a much smaller
narrow band oriented in the cross-track
direction below the source vessel.
Marine mammals that encounter the
Simrad EM120 at close range are
unlikely to be subjected to repeated
pulses because of the narrow fore-aft
width of the beam, and will receive only
limited amounts of pulse energy
because of the short pulses. In assessing
the possible impacts of the 15.5 kHz
Atlas Hydrosweep (a similar model),
Boebel et al. (2004) noted that the
critical sound pressure level at which
TTS may occur is 203.2 dB re 1 µPa
(rms). The critical region included an
area of 43 m (141 ft) in depth, 46 m (151
ft) wide athwartship, and 1 m (3.3 ft)
fore-and-aft (Boebel et al., 2004).
Behavioral reactions of free-ranging
marine mammals to military and other
sonars 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. However,
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all of those observations are of limited
relevance to the present situation. Pulse
durations from those sonars were much
longer than those of the SIO multi-beam
sonar, and a given mammal would have
received many pulses from the naval
sonars. During SIO’s operations, the
individual pulses will be very short, and
a given mammal would not receive
many of the downward-directed pulses
as the vessel passes by.
Captive bottlenose dolphins and a
white whale exhibited changes in
behavior when exposed to 1 s pulsed
sounds at frequencies similar to those
that will be emitted by the multi-beam
sonar 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). The
relevance of those data to free-ranging
odontocetes is uncertain, and in any
case, the test sounds were quite
different in either duration or
bandwidth as compared with those from
a bathymetric sonar.
Because of the shape of the beam,
NMFS believes it unlikely that marine
mammals will be exposed to the
bathymetric sonar at levels at or above
those likely to cause harassment.
Further, NMFS believes that the brief
exposure of cetaceans or pinnipeds to
one pulse, or small numbers of signals,
from the multi-beam bathymetric sonar
system are not likely to result in the
harassment of marine mammals.
Sub-bottom Profiler Signals
A sub-bottom profiler will be operated
from the source vessel at all times
during the planned study. Sounds from
the sub-bottom profiler are very short
pulses, occurring for 12 or 24 ms once
every 4.5–8 seconds. Most of the energy
in the sound pulses emitted by this subbottom profiler is at mid frequencies,
centered at 3.5 kHz. The beam width is
approximately 80o (cone-shaped) and is
directed downward.
The sub-bottom profiler on the Roger
Revelle has a stated maximum source
level of 211 dB re 1 µPa m (see section
I of SIO’s application). Thus, the
received level would be expected to
decrease to 180 dB and 160 dB
approximately 35 m and 350 m below
the transducer, respectively, assuming
spherical spreading. Corresponding
distances in the horizontal plane would
be substantially lower, given the
directionality of this source.
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
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if received at the same levels. However,
the pulsed signals from the sub-bottom
profiler are weaker than those from both
the multi-beam sonar and the two GI
guns. Behavioral responses are not
expected unless marine mammals are
very close to the source, e.g., within
approximately 350 m below the vessel,
or a lesser distance to the side. 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. 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. In the case of
mammals that do not avoid the
approaching vessel and its various
sound sources, mitigation measures that
would be applied to minimize effects of
the higher-power sources would further
reduce or eliminate any minor effects of
the sub-bottom profiler.
Because of the shape of the conical
beam and the power of the source,
NMFS believes it unlikely that marine
mammals will be exposed to the
bathymetric sonar at levels at or above
those likely to cause harassment.
Further, NMFS believes that the brief
exposure of cetaceans or pinnipeds to
small numbers of signals from the multibeam bathymetric sonar system are not
likely to result in the harassment of
marine mammals.
Estimated Take by Incidental
Harassment
All anticipated takes would be ‘‘takes
by harassment’’, involving temporary
changes in behavior. The proposed
mitigation measures are expected to
minimize the possibility of injurious
takes. (However, as noted earlier, there
is no specific information demonstrating
that injurious ‘‘takes’’ would occur even
in the absence of the planned mitigation
measures.) In the sections below, we
describe methods to estimate ‘‘take by
harassment’’, and present estimates of
the numbers of marine mammals that
might be affected during the proposed
seismic survey in the northeast Indian
Ocean. The estimates are based on the
best available data concerning marine
mammal densities (numbers per unit
area) and estimates of the size of the
area where effects potentially could
occur.
Because there is very little
information on marine mammal
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densities in the proposed survey area,
densities were used from two of
Longhurst’s (2007) biogeographic
provinces in the ETP that are
oceanographically similar to the two
provinces in which the seismic
activities will take place (see further,
below).
SIO’s application presents two types
of estimates: estimates of the number of
potential ‘‘exposures’’, and estimates of
the number of different individual
marine mammals that might potentially
be exposed to sound levels ≥160 dB re
1 µPa (rms). The distinction between
‘‘exposures’’ and ‘‘number of different
individuals exposed’’ is marginally
relevant in this project, because the plan
does not call for repeated GI gun
operations through the same or adjacent
waters, and the 2 GI guns that will be
used ensonify a relatively small area.
Estimates of the number of exposures
are considered precautionary
overestimates of the actual numbers of
different individuals potentially
exposed to seismic sounds, because in
all likelihood, exposures represent
repeated exposures of some of the same
individuals as discussed in the sections
that follow. Because of their
precautionary nature, the fact that they
are the numbers SIO requested
authorization for, and the fact that they
differ only slightly from the estimated
number of individuals, NMFS will use
the estimated number of exposures for
the take estimate.
The following estimates are based on
a consideration of the number of marine
mammals that might be disturbed
appreciably by operations with the 2 GI
guns to be used during approximately
2700 line-km of surveys at five sites on
the Ninety East Ridge in the
northeastern Indian Ocean. The
anticipated radii of influence of the
multi-beam sonar and sub-bottom
profiler are less than those for the GI
guns. It is assumed that, during
simultaneous operations of the multibeam sonar and airguns, any marine
mammals close enough to be affected by
the sonar would already be affected by
the airguns. No animals are expected to
exhibit more than short-term and
inconsequential responses to the multibeam sonar and sub-bottom profiler,
given their characteristics (e.g., narrow
downward-directed beam) and other
considerations described previously.
Therefore, no additional allowance is
included for animals that might be
affected by those sources. Any effects of
the multi-beam sonar and sub-bottom
profiler during times when they are
operating but the airguns are silent are
not considered.
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Few systematic aircraft- or ship-based
surveys have been conducted for marine
mammals in offshore waters of the
Indian Ocean, and the species of marine
mammals that occur there are not well
known. The density estimates used in
this assessment are from two sources, as
noted above. The most comprehensive
and recent density data available for
cetaceans of the ETP are from 1986 1996
NMFS ship surveys reported by
Ferguson and Barlow (2001).
(1) Some of those waters are in
Longhurst’s (2007) Pacific Equatorial
Divergence Province (PEQD), which is
similar to the Indian Monsoon Gyres
Province (MONS), in which 3 of the 5
proposed seismic surveys in the
northeastern Indian Ocean will occur.
The similarities are that they are both
high-nitrate, low-chlorophyll regions of
the oceans that support relatively large
populations of yellowfin, bigeye, and
skipjack tuna. SIO used the 1986 1996
data from blocks 162–170, 202–209, and
213–216 of Ferguson and Barlow (2001)
for the species group density estimates
given in Table 3 of SIO’s application
(and used to calculate the take estimates
in Table 1 here).
(2) Some of the surveys conducted by
Ferguson and Barlow (2001) in the ETP
are in Longhurst’s (2007) North Pacific
Tropical Gyre Province (NPTG), which
is similar to the Indian South
Subtropical Gyre Province (ISSG), in
which 2 of the 5 proposed seismic
surveys will occur. The similarities are
that they are both low-nitrate, lowchlorophyll regions of the oceans that
support relatively large bigeye and
yellowfin tuna populations. SIO used
the 1986 1996 data from blocks 105,
106, 111, 112, and 125 131 of Ferguson
and Barlow (2001) to compute the
species group densities in Table 4 of
their application (and used to calculate
the take estimates in Table 1 here).
The species that will be encountered
during the Indian Ocean survey will be
different than those sighted during the
surveys in the ETP. However, the
overall abundance of species groups
with generally similar habitat
requirements are expected to be roughly
similar. No density data were available
for any cetacean species in the proposed
seismic survey area. Thus, data from
offshore areas of the ETP to estimate the
densities of beaked whales, delphinids,
small whales, and mysticetes in the
northeastern Indian Ocean were used.
SIO then estimated the relative
abundance of individual species within
the species groups on a scale of 1 (rare)
to 10 (abundant) using various surveys
and other information from areas near
the study area, and general information
on species such as latitudinal ranges,
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water depth preferences, and group
sizes (see Column 1 in Tables 3 and 4
of SIO’s application). Finally, SIO
estimated the density of each species
expected to occur in the survey area
from the densities for species groups in
Tables 3 and 4 of their application by
multiplying their relative abundance/
the relative abundance for all species in
the species group times the density for
the species group.
Tables 3 and 4 in SIO’s application
give the average and maximum densities
for each species group of marine
mammals reported in the PEQD and
NPTG provinces of the ETP, corrected
for effort, based on the densities
reported in Ferguson and Barlow (2001).
The densities from those studies had
been corrected, by the original authors,
for both detectability bias and
availability bias. Detectability bias is
associated with diminishing sightability
with increasing lateral distance from the
track line [f(0)]. Availability bias refers
to the fact that there is less-than 100
percent probability of sighting an
animal that is present along the survey
track line, and it is measured by g(0).
It should be noted that the following
estimates of ‘‘takes by harassment’’
assume that the seismic surveys will be
undertaken and completed; in fact, the
planned number of line-kms has been
increased by 25 percent to accommodate
lines that may need to be repeated,
equipment testing, etc. As is typical on
offshore ship surveys, inclement
weather, equipment malfunctions, and
other survey priorities (rock dredging,
magnetic surveys) may cause delays and
may limit the number of useful line-kms
of seismic operations that can be
undertaken. Furthermore, any marine
mammal sightings within or near the
designated safety zones will result in
the shut down of seismic operations as
a mitigation measure. Thus, the
following estimates of the numbers of
marine mammals potentially exposed to
160–dB sounds are precautionary, and
probably overestimate the actual
numbers of marine mammals that might
be involved. The estimates assume that
there are no conflicts in survey
priorities or weather, equipment, or
mitigation delays, which is unlikely,
particularly given the complexity of the
tasks and equipment involved.
There is some uncertainty about the
representativeness of the data and the
assumptions used in the take
calculations. However, the approach
used here is believed to be the best
available approach. Also, to provide
some allowance for the uncertainties,
‘‘maximum estimates’’ as well as ‘‘best
estimates’’ of the numbers potentially
affected have been derived. Best and
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maximum estimates are based on the
average and maximum estimates of
densities reported in the selected
datasets that were used from Ferguson
and Barlow (2001) described above. SIO
has requested authorization for the take
of the maximum estimates and NMFS
has analyzed the maximum estimate for
it’s effect on the species or stock.
The potential number of occasions
when members of each species might be
exposed to received levels ≥160 dB re 1
µPa (rms) was calculated by multiplying
• Its expected density, either
‘‘average’’ (i.e., best) or ‘‘maximum’’,
corrected as described above, times
• The anticipated total linekilometers of operations with the 2 GI
guns (including turns and additional
buffer line km to allow for repeating of
lines due to equipment malfunction,
bad weather, etc.), times
• The cross-track distances within
which received sound levels are
predicted to be ≥160 dB.
For the 2 GI guns, that cross track
distance is 2x the predicted 160–dB
radii of 400 m (1312 ft) in water depths
>1000 m (3280 ft).
Based on that method, the ‘‘best’’ and
‘‘maximum’’ estimates of the number of
marine mammal exposures to airgun
sounds ≥160 dB re 1 µPa (rms) were
obtained for each of the ecological
provinces using the reported average
and maximum densities from Tables 3
and 4 of SIO’s application. The two
estimates were then added to give totals.
Of the five endangered cetacean species
that could be present, the best and
maximum estimates show that only one
blue whale and one sperm whale may
be exposed to such noise levels (Table
5 of SIO’s application). The vast
majority of the best and maximum
exposures to seismic sounds ≥160 dB
would involve delphinids. Maximum
estimates of exposures for the species
with the highest numbers are, in
descending order, spinner dolphin (215
exposures), common and Risso’s
dolphins (151 exposures), and
bottlenose dolphin (129 exposures).
Estimates for other species are lower
(Table 1).
The far right column in Table 1,
‘‘Requested Take Authorization’’, shows
the numbers for which ‘‘take
authorization’’ is requested. The
requested take authorization numbers
are calculated as indicated above based
on the maximum densities reported by
Ferguson and Barlow (2001) in any of
the survey blocks included in the
average density estimates. For those
species for which very low numbers to
none are estimated to be exposed to
seismic sounds ≥160 dB, SIO included
allowance for encountering one group
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based on the mean group size. Where
group sizes are less than five, SIO
assigned a group size of five. However,
for endangered species, NMFS only
plans to authorize take for one sperm
whale and one blue whale.
The best and maximum estimates are
based on 160–dB distances predicted
from the acoustic model applied by LDEO. Based on the empirical calibration
data collected in the Gulf of Mexico in
2003 for L-DEO’s 2 GI guns in deep
water (510 m (1673 ft)), actual 160–dB
distances in deep water are likely to be
less than predicted (Tolstoy et al.,
2004). Additionally, the requested take
is based on maximum exposure
estimates (based on maximum density
estimates). Given these considerations,
the predicted numbers of marine
mammals that might be exposed to
sounds ≥160 dB may be somewhat
overestimated.
The stock structures of the marine
mammals present in the Indian Ocean
have not been identified by NMFS;
therefore, NMFS must make the
necessary findings based on the species
as a whole. The species anticipated to
be affected during the proposed
activities are wide-ranging species.
Though worldwide abundance (or
abundance outside of that estimated for
the U.S. stocks) has not been estimated,
localized surveys in the west tropical
Indian Ocean and elsewhere have been
conducted. Since the take estimates
proposed in this document fall largely
within 6 percent (all but common
dolphin (21 percent) and rough-toothed
dolphin (14 percent)) of the numbers
estimated to be present during a
localized survey of the west tropical
Indian Ocean, and the species range far
beyond the Indian Ocean (i.e., the
abundance of the species is notably
larger), NMFS believes that the
estimated take numbers for these are
small relative both to the worldwide
abundance of these species and to
numbers taken in other activities that
have been authorized for incidental take
of these species.
Potential Effects on Habitat
The proposed airgun operations will
not result in any permanent impact on
habitats used by marine mammals, or to
the food sources they use. The main
impact issue associated with the
proposed activities will be temporarily
elevated noise levels and the associated
direct effects on marine mammals, as
discussed above.
One of the reasons for the adoption of
airguns as the standard energy source
for marine seismic surveys was that they
(unlike the explosives used in the
distant past) do not result in any
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appreciable fish kill. However, the
existing body of information relating to
the impacts of seismic on marine fish
and invertebrate species is very limited.
The various types of potential effects of
exposure to seismic on fish and
invertebrates can be considered in three
categories: (1) pathological, (2)
physiological, and (3) behavioral.
Pathological effects include lethal and
sub-lethal damage to the animals,
physiological effects include temporary
primary and secondary stress responses,
and behavioral effects refer to changes
in exhibited behavior of the fish and
invertebrates. The three categories are
interrelated in complex ways. For
example, it is possible that certain
physiological and behavioral changes
could potentially lead to the ultimate
pathological effect on individual
animals (i.e., mortality).
The available information on the
impacts of seismic surveys on marine
fish and invertebrates provides limited
insight on the effects only at the
individual level. Ultimately, the most
important knowledge in this area relates
to how significantly seismic affects
animal populations.
The following sections provide an
overview of the information that exists
on the effects of seismic surveys on fish
and invertebrates. The information
comprises results from scientific studies
of varying degrees of soundness and
some anecdotal information.
Pathological Effects – 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 (Hubbs and Rechnitzer, 1952 in
Wardle et al., 2001). Generally, the
higher the received pressure and the
less time it takes for the pressure to rise
and decay, the greater the chance of
acute pathological effects. Considering
the peak pressure and rise/decay time
characteristics of seismic airgun arrays
used today, the pathological zone for
fish and invertebrates would be
expected to be within a few meters of
the seismic source (Buchanan et al.,
2004). For the proposed survey, any
injurious effects on fish would be
limited to very short distances,
especially considering the small source
planned for use in this project (two 45–
in3 GI guns).
Matishov (1992) reported that some
cod and plaice died within 48 hours of
exposure to seismic pulses 2 m (6.5 ft)
from the source. No other details were
provided by the author. On the other
hand, there are numerous examples of
no fish mortality as a result of exposure
to seismic sources (Falk and Lawrence
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1973; Holliday et al., 1987; La Bella et
al., 1996; Santulli et al., 1999; McCauley
et al., 2000a, 2000b; Bjarti, 2002; IMG,
2002; McCauley et al., 2003; Hassel et
al., 2003).
There are examples of damage to fish
ear structures from exposure to seismic
airguns (McCauley et al., 2000a, 2000b,
2003), but it should be noted the
experimental fish were caged and
exposed to high cumulative levels of
seismic energy. Atlantic salmon were
exposed within 1.5 m (4.9 ft) of
underwater explosions (Sverdrup et al.,
1994). Compared to airgun sources,
explosive detonations are characterized
by higher peak pressures and more
rapid rise and decay times, and are
considered to have greater potential to
damage marine biota. In spite of this, no
salmon mortality was observed
immediately after exposure or during
the seven-day monitoring period
following exposure.
Some studies have also provided
some information on the effects of
seismic exposure on fish eggs and larvae
(Kostyuchenko, 1972; Dalen and
Knutsen, 1986; Holliday et al., 1987;
Matishov, 1992; Booman et al., 1996;
Dalen et al., 1996). Overall, impacts
appeared to be minimal and any
mortality was generally not significantly
different from the experimental
controls. Generally, any observed larval
mortality occurred after exposures
within 0.5 3 m (1.6–9.8 ft) of the airgun
source. Matishov (1992) did report some
retinal tissue damage in cod larvae
exposed at 1 m (3.3 ft) from the airgun
source. Saetre and Ona (1996) applied a
’worst-case scenario’ mathematical
model to investigate the effects of
seismic energy on fish eggs and larvae,
and concluded that mortality rates
caused by exposure to seismic are so
low compared to natural mortality that
the impact of seismic surveying on
recruitment to a fish stock must be
regarded as insignificant.
The pathological impacts of seismic
energy on marine invertebrate species
have also been investigated. Christian et
al. (2003) exposed adult male snow
crabs, egg-carrying female snow crabs,
and fertilized snow crab eggs to energy
from seismic airguns. Neither acute nor
chronic (12 weeks after exposure)
mortality was observed for the adult
male and female crabs. There was a
significant difference in development
rate noted between the exposed and
unexposed fertilized eggs. The egg mass
exposed to seismic energy had a higher
proportion of less-developed eggs than
the unexposed mass. It should be noted
that both egg masses came from a single
female and that any measure of natural
variability was unattainable. However, a
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result such as this does point to the
need for further study.
Pearson et al. (1994) exposed Stage II
larvae of the Dungeness crab to single
discharges from a seven-airgun seismic
array and compared their mortality and
development rates with those of
unexposed larvae. For immediate and
long-term survival and time to molt, this
field experiment did not reveal any
statistically-significant differences
between the exposed and unexposed
larvae, even those exposed within 1 m
(3.3 ft) of the seismic source.
Bivalves of the Adriatic Sea were also
exposed to seismic energy and
subsequently assessed (LaBella et al.,
1996). No effects of the exposure were
noted.
To date, there have not been any welldocumented cases of acute post-larval
fish or invertebrate mortality as a result
of exposure to seismic sound under
normal seismic operating conditions.
Sub-lethal injury or damage has been
observed, but generally as a result of
exposure to very high received levels of
sound, significantly higher than the
received levels generated by the single
GI gun sound source to be used in the
proposed study. Acute mortality of eggs
and larvae have been demonstrated in
experimental exposures, but only when
the eggs and larvae were exposed very
close to the seismic sources and the
received pressure levels were
presumably very high. Limited
information has not indicated any
chronic mortality as a direct result of
exposure to seismic.
Physiological Effects – Biochemical
responses by marine fish and
invertebrates to acoustic stress have also
been studied, although in a limited way.
Studying the variations in the
biochemical parameters influenced by
acoustic stress might give some
indication of the extent of the stress and
perhaps forecast eventual detrimental
effects. Such stress could potentially
affect animal populations by reducing
reproductive capacity and adult
abundance.
McCauley et al. (2000a, 2000b) used
various physiological measures to study
the physiological effects of exposure to
seismic energy on various fish species,
squid, and cuttlefish. No significant
physiological stress increases
attributable to seismic energy were
detected. Sverdrup et al. (1994) found
that Atlantic salmon subjected to
acoustic stress released primary stress
hormones, adrenaline and cortisol, as a
biochemical response although there
were different patterns of delayed
increases for the different indicators.
Caged European sea bass were exposed
to seismic energy and numerous
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biochemical responses were indicated.
All returned to their normal
physiological levels within 72 hours of
exposure.
Stress indicators in the haemolymph
of adult male snow crabs were
monitored after exposure of the animals
to seismic energy (Christian et al.,
2003). No significant differences
between exposed and unexposed
animals were found in the stress
indicators (e.g., proteins, enzymes, cell
type count).
Primary and secondary stress
responses of fish after exposure to
seismic energy all appear to be
temporary in any studies done to date.
The times necessary for these
biochemical changes to return to normal
are variable depending on numerous
aspects of the biology of the species and
of the sound stimulus.
Summary of Physical (Pathological
and Physiological) Effects – As
indicated in the preceding general
discussion, there is a relative lack of
knowledge about the potential physical
(pathological and physiological) effects
of seismic energy on marine fish and
invertebrates. Available data suggest
that there may be physical impacts on
egg, larval, juvenile, and adult stages at
very close range. Considering typical
source levels associated with
commercial seismic arrays, close
proximity to the source would result in
exposure to very high energy levels.
Again, this study will employ a sound
source that will generate low energy
levels. Whereas egg and larval stages are
not able to escape such exposures,
juveniles and adults most likely would
avoid it. In the case of eggs and larvae,
it is likely that the numbers adversely
affected by such exposure would not be
that different from those succumbing to
natural mortality. Limited data
regarding physiological impacts on fish
and invertebrates indicate that these
impacts are short term and are most
apparent after exposure at close range.
The proposed seismic program for
2007 is predicted to have negligible to
low physical effects on the various life
stages of fish and invertebrates for its
short duration (approximately 49 hours
at each of five sites on the Ninety East
Ridge) and 2700–km extent. Therefore,
physical effects of the proposed program
on the fish and invertebrates would be
not significant.
Fish and Invertebrate Acoustic
Detection and Production – Hearing in
fishes was first demonstrated in the
early 1900s through studies involving
cyprinids (Parker, 1903 and Bigelow,
1904 in Kenyon et al., 1998). Since that
time, numerous methods have been
used to test auditory sensitivity in
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fishes, resulting in audiograms of over
50 species. These data reveal great
diversity in fish hearing ability, mostly
attributable to various peripheral modes
of coupling the ear to internal
structures, including the swim bladder.
However, the general auditory
capabilities of <0.2 percent of fish
species are known so far.
For many years, studies of fish
hearing have reported that the hearing
bandwidth typically extends from below
100 Hz to approximately 1 kHz in fishes
without specializations for sound
detection, and up to approximately 7
kHz in fish with specializations that
enhance bandwidth and sensitivity.
Recently there have been suggestions
that certain fishes, including many
clupeiforms (herring, shads, anchovies,
etc.) may be capable of detecting
ultrasonic signals with frequencies as
high as 126 kHz (Dunning et al., 1992;
Nestler et al., 1992). Studies on Atlantic
cod, a non-clupeiform fish, suggested
that this species could detect ultrasound
at almost 40 kHz (Astrup and M hl,
1993).
Mann et al. (2001) showed that the
American shad is capable of detecting
sounds up to 180 kHz. They also
demonstrated that the gulf menhaden is
also able to detect ultrasound, whereas
other species such as the bay anchovy,
scaled sardine, and Spanish sardine
only detect sounds with frequencies up
to approximately 4 kHz.
Among fishes, at least two major
pathways for sound transmission to the
ear have been identified. The first and
most primitive is the conduction of
sound directly from the water to tissue
and bone. The fish’s body takes up the
sound’s acoustic particle motion and
subsequent hair cell stimulation occurs
because of the difference in inertia
between the hair cells and their
overlying otoliths. These species are
known as ’hearing generalists’ (Fay and
Popper, 1999). The second sound
pathway to the ears is indirect. The
swim bladder or other gas bubble near
the ears expands and contracts in
volume in response to sound pressure
fluctuations, and the motion is then
transmitted to the otoliths. While
present in most bony fishes, the swim
bladder is absent or reduced in many
other fish species. Only some species of
fish with a swim bladder appear to be
sound-pressure sensitive via this
indirect pathway to the ears; they are
called ’hearing specialists’. Hearing
specialists have some sort of connection
with the inner ear, either via bony
structures known as Weberian ossicles,
extensions of the swim bladder, or a
swim bladder more proximate to the
inner ear. Hearing specialists’ sound-
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pressure sensitivity is high and their
upper frequency range of detection is
extended above those species that hear
only by the direct pathway. Typically,
most fish detect sounds of frequencies
up to 2,000–Hz but, as indicated, others
have detection ranges that extend to
much higher frequencies.
Fish also possess lateral lines that
detect water movements. The essential
stimulus for the lateral line consists of
differential water movement between
the body surface and the surrounding
water. The lateral line is typically used
in concert with other sensory
information, including hearing (Sand,
1981; Coombs and Montgomery, 1999).
Elasmobranchs (sharks and skates)
lack any known pressure-todisplacement transducers such as swim
bladders. Therefore, they presumably
must rely on the displacement
sensitivity of their mechanoreceptive
cells. Unlike acoustic pressure, the
kinetic stimulus is inherently
directional but its magnitude rapidly
decreases relative to the pressure
component as it propagates outward
from the sound source in the near field.
It is believed that elasmobranches are
most sensitive to low frequencies, those
<1 kHz (Corwin 1981).
Because they lack air-filled cavities
and are often the same density as water,
invertebrates detect underwater
acoustics differently than fish. Rather
than being pressure sensitive,
invertebrates appear to be most sensitive
to particle displacement. However, their
sensitivity to particle displacement and
hydrodynamic stimulation seem poor
compared to fish. Decapods, for
example, have an extensive array of
hair-like receptors both within and
upon the body surface that could
potentially respond to water- or
substrate-borne displacements. They are
also equipped with an abundance of
proprioceptive organs that could serve
secondarily to perceive vibrations.
Crustaceans appear to be most sensitive
to sounds of low frequencies, those
<1000 Hz (Budelmann, 1992; Popper et
al., 2001).
Many fish and invertebrates are also
capable of sound production. It is
believed that these sounds are used for
communication in a wide range of
behavioral and environmental contexts.
The behaviors most often associated
with acoustic communication include
territorial behavior, mate finding,
courtship, and aggression. Sound
production provides a means of longdistance communication and
communication when underwater
visibility is poor (Zelick et al., 1999).
Behavioral Effects – Because of the
apparent lack of serious pathological
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and physiological effects of seismic
energy on marine fish and invertebrates,
most concern now centers on the
possible effects of exposure to seismic
surveys on the distribution, migration
patterns, and catchability of fish. There
is a need for more information on
exactly what effects such sound sources
might have on the detailed behavior
patterns of fish and invertebrates at
different ranges. Studies investigating
the possible effects of seismic energy on
fish and invertebrate behavior have been
conducted on both uncaged and caged
animals. Studies of change in catch rate
regard potential effects of seismic
energy on larger spatial and temporal
scales than are typical for close-range
studies that often involve caged animals
(Hirst and Rodhouse, 2000). Hassel et al.
(2003) investigated the behavioral
effects of seismic pulses on caged sand
lance in Norwegian waters. The sand
lance did exhibit responses to the
seismic, including an increase in
swimming rate, an upwards vertical
shift in distribution, and startle
responses. Normal behaviors were
resumed shortly after cessation of the
seismic source. None of the observed
sand lance reacted by burying into the
sand.
Engas et al. (1996) assessed the effects
of seismic surveying on Atlantic cod
and haddock behavior using acoustic
mapping and commercial fishing
techniques. Results indicated that fish
abundance decreased at the seismic
survey area, and that the decline in
abundance and catch rate lessened with
distance from the survey area. Fish
abundance and catch rates had not
returned to pre-shooting levels five days
after cessation of shooting. In other
airgun experiments, catch per unit effort
(CPUE) of demersal fish declined when
airgun pulses were emitted, particularly
in the immediate vicinity of the seismic
survey (Dalen and Raknes, 1985; Dalen
and Knutsen, 1986; L kkeborg, 1991;
Skalski et al., 1992). Reductions in the
catch may have resulted from a change
in behavior of the fish. The fish schools
descended to near the bottom when the
airgun was firing, and the fish may have
changed their swimming and schooling
behavior. Fish behavior returned to
normal minutes after the sounds ceased.
Marine fish inhabiting an inshore reef
off the coast of Scotland were monitored
by telemetry and remote camera before,
during, and after airgun firing (Wardle
et al., 2001). Although some startle
responses were observed, the seismic
gun firing had little overall effect on the
day-to-day behavior of the resident fish.
Other species involved in studies that
have indicated fish behavioral responses
to underwater sound include rockfish
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(Pearson et al., 1992), Pacific herring
(Schwarz and Greer, 1984), and Atlantic
herring (Blaxter et al., 1981). The
responses observed in these studies
were relatively temporary. What is not
known is the effect of exposure to
seismic energy on fish and invertebrate
behaviors that are associated with
reproduction and migration.
Studies on the effects of sound on fish
behavior have also been conducted
using caged or confined fish. Such
experiments were conducted in
Australia using fish, squid, and
cuttlefish as subjects (McCauley et al.
(2000a,b). Common observations of fish
behavior included startle response,
faster swimming, movement to the part
of the cage furthest from the seismic
source (i.e., avoidance), and eventual
habituation. Fish behavior appeared to
return pre-seismic state 15 30 min after
cessation of seismic shooting. Squid
exhibited strong startle responses to the
onset of proximate airgun firing by
releasing ink and/or jetting away from
the source. The squid consistently made
use of the ’sound shadow’ at the surface,
where the sound intensity was less than
at 3–m (9.8 ft) depth. These Australian
experiments provided more evidence
that fish and invertebrate behavior will
be modified at some received sound
level. Again, the behavioral changes
seem to be temporary.
Christian et al. (2003) conducted an
experimental commercial fishery for
snow crab before and after the area was
exposed to seismic shooting. Although
the resulting data were not conclusive,
no drastic decrease in catch rate was
observed after seismic shooting
commenced. Another behavioral
investigation by Christian et al. (2003)
involved caging snow crabs, positioning
the cage 50 m (164 ft) below a seven-gun
array, and observing the immediate
responses of the crabs to the onset of
seismic shooting by remote underwater
camera. No obvious startle behaviors
were observed. Anecdotal information
from Newfoundland, Canada, indicated
that snow crab catch rates showed a
significant reduction immediately
following a pass by a seismic survey
vessel. Other anecdotal information
from Newfoundland indicated that a
school of shrimp showing on a fishing
vessel sounder shifted downwards and
away from a nearby seismic source.
Effects were temporary in both the snow
crab and shrimp anecdotes (Buchanan et
al., 2004).
Summary of Behavioral Effects – As is
the case with pathological and
physiological effects of seismic on fish
and invertebrates, available information
is relatively scant and often
contradictory. There have been well-
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documented observations of fish and
invertebrates exhibiting behaviors that
appeared to be responses to exposure to
seismic energy (i.e., startle response,
change in swimming direction and
speed, and change in vertical
distribution), but the ultimate
importance of those behaviors is
unclear. Some studies indicate that such
behavioral changes are very temporary,
whereas others imply that fish might not
resume pre-seismic behaviors or
distributions for a number of days.
There appears to be a great deal of interand intra-specific variability. In the case
of finfish, three general types of
behavioral responses have been
identified: startle, alarm, and avoidance.
The type of behavioral reaction appears
to depend on many factors, including
the type of behavior being exhibited
before exposure, and proximity and
energy level of sound source.
During the proposed study, only a
small fraction of the available habitat
would be ensonified at any given time,
and fish species would return to their
pre-disturbance behavior once the
seismic activity ceased. The proposed
seismic program is predicted to have
negligible to low behavioral effects on
the various life stages of the fish and
invertebrates during its short duration
(approximately 49 hours at each of 5
sites on the Ninety East Ridge) and
2700–km extent.
Changes in behavior in fish near the
airguns might have short-term impacts
on the ability of cetaceans to feed near
the survey area. However, only a small
fraction of the available habitat would
be ensonified at any given time, and fish
species would return to their predisturbance behavior once the seismic
activity ceased. Thus, the proposed
survey would have little impact on the
abilities of marine mammals to feed in
the area where seismic work is planned.
Some of the fish that do not avoid the
approaching airguns (probably a small
number) may be subject to auditory or
other injuries.
Zooplankters that are very close to the
source may react to the shock wave.
These animals have an exoskeleton and
no air sacs. Little or no mortality is
expected. Many crustaceans can make
sounds and some crustaceans and other
invertebrates have some type of sound
receptor. However, the reactions of
zooplankters to sound are not known.
Some mysticetes feed on concentrations
of zooplankton. A reaction by
zooplankton to a seismic impulse would
only be relevant to whales if it caused
a concentration of zooplankton to
scatter. Pressure changes of sufficient
magnitude to cause this type of reaction
would probably occur only very close to
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the source. Impacts on zooplankton
behavior are predicted to be negligible,
and this would translate into negligible
impacts on feeding mysticetes.
Because of the reasons noted above
and the nature of the proposed activities
(small airguns and limited duration), the
proposed operations are not expected to
have any habitat-related effects that
could cause significant or long-term
consequences for individual marine
mammals or their populations or stocks.
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Monitoring
Either dedicated marine mammal
observers (MMOs) or other vessel-based
personnel will watch for marine
mammals near the seismic source vessel
during all daytime and nighttime airgun
operations. GI airgun operations will be
suspended when marine mammals are
observed within, or about to enter,
designated safety radii where there is a
possibility of significant effects on
hearing or other physical effects. At
least one dedicated vessel-based MMO
will watch for marine mammals near the
seismic vessel during daylight periods
when shooting is being conducted, and
two MMOs will watch for marine
mammals for at least 30 min prior to
start-up of airgun operations.
Observations of marine mammals will
also be made and recorded during any
daytime periods without airgun
operations. At night, the forwardlooking bridge watch of the ship’s crew
will look for marine mammals that the
vessel is approaching, and execute
avoidance maneuvers; the 180dB/190dB
safety radii around the airguns will be
continuously monitored by an aftlooking member of the scientific party,
who will call for shutdown of the guns
if mammals are observed within the
safety radii. Nighttime observers will be
aided by (aft-directed) ship’s lights and
night vision devices (NVDs).
Observers will be appointed by SIO
with NMFS concurrence. Two observers
will be on the vessel, and both will have
gone through NOAA/NMFS training for
marine mammal observations. Observers
will be on duty in shifts usually of
duration no longer than two hours. Use
of two simultaneous observers prior to
start up will increase the detectability of
marine mammals present near the
source vessel, and will allow
simultaneous forward and rearward
observations. Bridge personnel
additional to the dedicated marine
mammal observers will also assist in
detecting marine mammals and
implementing mitigation requirements,
and before the start of the seismic
survey will be given instruction in how
to do so.
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The Roger Revelle is a suitable
platform for marine mammal
observations, and has been used for that
purpose during the routine CalCOFI
(California Cooperative Oceanic
Fisheries Investigations). Observing
stations will be at the 02 level, with
observers’ eyes approximately 10.4 m
(34 ft) above the waterline: one forward
on the 02 deck commanding a forwardcentered, approximately 240° view, and
one atop the aft hangar, with an aftcentered view that includes the 60–m
radius area around the airguns. The eyes
of the bridge watch will be at a height
of approximately 15 m (49 ft); marine
mammal observers will repair to the
enclosed bridge and adjoining aft
steering station during any inclement
weather (unlikely at this place and
season), and as necessary to use the 50
X ‘‘big-eye’’ binoculars that are mounted
there.
Standard equipment for marine
mammal observers will be 7 X 50 reticle
binoculars and optical range finders. At
night, night vision equipment will be
available. The observers will be in
wireless 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 airgun powerdown or shut-down.
The vessel-based monitoring will
provide data required to estimate the
numbers of marine mammals exposed to
various received sound levels, to
document any apparent disturbance
reactions, and thus to estimate the
numbers of mammals potentially
‘‘taken’’ by harassment. It will also
provide the information needed in order
to shut down the GI airguns at times
when mammals are present in or near
the safety zone. When a mammal
sighting is made, the following
information about the sighting will 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
seismic vessel (e.g., none, avoidance,
approach, paralleling, etc.), and
behavioral pace.
(2) Time, location, heading, speed,
activity of the vessel (shooting or not),
sea state, visibility, cloud cover, and sun
glare.
The data listed under (2) will also be
recorded at the start and end of each
observation watch and during a watch,
whenever there is a change in one or
more of the variables.
All mammal observations and airgun
shutdowns will be recorded in a
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standardized format. Data will be
entered into a custom database using a
notebook computer when observers are
off duty. The accuracy of the data entry
will be verified by computerized data
validity checks as the data are entered,
and by subsequent manual checking of
the database. Those procedures will
allow initial summaries of data to be
prepared during and shortly after the
field program, and will facilitate transfer
of the data to statistical, graphical, or
other programs for further processing
and archiving.
Results from the vessel-based
observations will provide:
• The basis for real-time mitigation
(airgun shut down).
• Information needed to estimate the
number of marine mammals potentially
taken by harassment, which must be
reported to NMFS.
• Data on the occurrence,
distribution, and activities of marine
mammals in the area where the seismic
study is conducted.
• Information to compare the distance
and distribution of marine mammals
relative to the source vessel at times
with and without seismic activity.
• Data on the behavior and movement
patterns of marine mammals seen at
times with and without seismic activity.
Mitigation
For the proposed seismic surveys in
the Northeastern Indian Ocean during
May August 2007, SIO will deploy two
GI airguns as an energy source, with a
total discharge volume of 90 in3. The
energy from the airguns will be directed
mostly downward. The small size of the
airguns to be used during the proposed
study will reduce the potential for
effects relative to those that might occur
with a large airgun arrays.
In addition to marine mammal
monitoring, the following mitigation
measures will be adopted during the
proposed seismic program, provided
that doing so will not compromise
operational safety requirements.
Although power-down procedures are
often standard operating practice for
seismic surveys, it will not be used here
because powering down from two guns
to one gun would make only a small
difference in the 180- or 190–dB radius
– probably not enough to allow
continued one-gun operations if a
mammal came within the safety radius
for two guns. Mitigation measures that
will be adopted are:
(1) Speed or course alteration;
(2) Ramp-up and shut-down
procedures; and
(3) Night operations;
Speed or Course Alteration – If a
marine mammal is detected outside the
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safety radius and, based on its position
and the relative motion, is likely to
enter the safety radius, the vessel’s
speed and/or direct course may, when
practical and safe, be changed in a
manner that also minimizes the effect to
the planned science objectives. The
marine mammal activities and
movements relative to the seismic vessel
will be closely monitored to ensure that
the animal does not approach within the
safety radius. If the animal appears
likely to enter the safety radius, further
mitigative actions will be taken, i.e.
either further course alterations or shut
down of the airguns.
Shut-down Procedures - If a marine
mammal is detected outside the safety
radius but is likely to enter the safety
radius, and if the vessel’s course and/or
speed cannot be changed to avoid
having the animal enter the safety
radius, the airguns will be shut down
before the animal is within the safety
radius (10 m (33 ft) for pinnipeds (190–
dB isopleth) or 40 m (131 ft) for
cetaceans (180–dB isopleth)). Likewise,
if a marine mammal is already within
the safety radius when first detected, the
airguns will be shut down immediately.
Airgun activity will not resume until
the animal has cleared the safety radius.
The animal will be considered to have
cleared the safety radius if it is visually
observed to have left the safety radius,
or if it has not been seen within the
radius for 15 min (small odontocetes
and pinnipeds) or 30 min (mysticetes
and large odontocetes, including sperm,
pygmy sperm, dwarf sperm, beaked, and
bottlenose whales).
Ramp-up Procedures – A ‘‘ramp-up’’
procedure will be followed when the
airguns begin operating after a period
without airgun operations. The two GI
guns will be added in sequence 5
minutes apart. During ramp-up
procedures, the safety radius for the two
GI guns will be maintained.
Night Operations – At night, vessel
lights and/or night vision devices
(NVDs) could be useful in sighting some
marine mammals at the surface within
a short distance from the ship (within
the safety radii for the two GI guns in
deep water). Start up of the airguns will
only occur in situations when the entire
safety radius is visible with vessel lights
and NVDs.
Reporting
A report will be submitted to NMFS
within 90 days after the end of the
cruise. The end of the northeastern
Indian Ocean cruise is predicted to
occur between July 16 and August 13,
2007. The report will describe the
operations that were conducted and the
marine mammals that were detected
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near the operations. The report will be
submitted to NMFS, providing full
documentation of methods, results, and
interpretation pertaining to all
monitoring. The 90–day report will
summarize the dates and locations of
seismic operations, marine mammal
sightings (dates, times, locations,
activities, associated seismic survey
activities), and estimates of the amount
and nature of potential ‘‘take’’ of marine
mammals by harassment or in other
ways.
Endangered Species Act
Under section 7 of the Endangered
Species Act (ESA) the NSF has begun
consultation on this proposed seismic
survey. NMFS will also consult on the
issuance of an IHA under section
101(a)(5)(D) of the MMPA for this
activity. Consultation will be concluded
prior to a determination on the issuance
of the IHA.
National Environmental Policy Act
(NEPA)
NSF prepared an Environmental
Assessment of a Planned Low-Energy
Marine Seismic Survey by the Scripps
Institution of Oceanography in the
Northeast Indian Ocean, May July 2007.
NMFS will either adopt NSF’s EA or
conduct a separate NEPA analysis, as
necessary, prior to making a
determination on the issuance of the
IHA.
Preliminary Determinations
NMFS has preliminarily determined
that the impact of conducting the
seismic survey in the northeast Indian
Ocean may result, at worst, in a
temporary modification in behavior
(Level B Harassment) of small numbers
of 29 species of cetaceans. Further, this
activity is expected to result in a
negligible impact on the affected species
or stocks. The provision requiring that
the activity not have an unmitigable
adverse impact on the availability of the
affected species or stock for subsistence
uses does not apply for this proposed
action.
For reasons stated peviously in this
document, this determination is
supported by: (1) the likelihood that,
given sufficient notice through
relatively slow ship speed and rampup,
marine mammals are expected to move
away from a noise source that is
annoying prior to its becoming
potentially injurious; (2) the fact that
marine mammals would have to be
closer than 40 m from the vessel to be
exposed to levels of sound (180 dB)
believed to have even a minimal chance
of causing TTS; and (3) the likelihood
that marine mammal detection ability
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by trained observers is high at that short
distance from the vessel. As a result, no
take by injury or death is anticipated
and the potential for temporary or
permanent hearing impairment is very
low and will be avoided through the
incorporation of the proposed
mitigation measures.
While the number of potential
incidental harassment takes will depend
on the distribution and abundance of
marine mammals in the vicinity of the
survey activity, the number of potential
harassment takings is estimated to be
small, less than a few percent of any of
the estimated population sizes, and has
been mitigated to the lowest level
practicable through incorporation of the
measures mentioned previously in this
document.
Proposed Authorization
As a result of these preliminary
determinations, NMFS proposes to issue
an IHA to SIO for conducting a lowenergy seismic survey in the Indian
Ocean from May - August, 2007,
provided the previously mentioned
mitigation, monitoring, and reporting
requirements are incorporated.
Dated: April 4, 2007.
David Cottingham,
Acting Deputy Director, Office of Protected
Resources, National Marine Fisheries Service.
[FR Doc. E7–6750 Filed 4–9–07; 8:45 am]
BILLING CODE 3510–22–S
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
[I.D. 010207B]
Small Takes of Marine Mammals
Incidental to Specified Activities;
Seismic Surveys in the Beaufort and
Chukchi Seas off Alaska
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice of receipt of application
and proposed incidental take
authorization; request for comments.
AGENCY:
SUMMARY: NMFS has received an
application from Shell Offshore, Inc.
(SOI) for an Incidental Harassment
Authorization (IHA) to take small
numbers of marine mammals, by
harassment, incidental to conducting
open-water offshore exploratory drilling
on Outer Continental Shelf (OCS) oil
lease blocks in the Beaufort Sea off
Alaska. Under the Marine Mammal
Protection Act (MMPA), NMFS is
requesting comments on its proposal to
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10APN1
Agencies
[Federal Register Volume 72, Number 68 (Tuesday, April 10, 2007)]
[Notices]
[Pages 17849-17864]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-6750]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
[I.D. 040307B]
Small Takes of Marine Mammals Incidental to Specified Activities;
Low-Energy Marine Seismic Survey in the Northeastern Indian Ocean, May-
August 2007
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental take authorization; request for
comments.
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SUMMARY: NMFS has received an application from Scripps Institute of
Oceanography (SIO) for an Incidental Harassment Authorization (IHA) to
take marine mammals incidental to conducting a low-energy marine
seismic survey in the northeastern Indian Ocean during May-August 2007.
Pursuant to the Marine Mammal Protection Act (MMPA), NMFS is requesting
comments on its proposal to issue an IHA to SIO to incidentally take,
by Level B harassment only, several species of marine mammals during
the aforementioned activity.
DATES: Comments and information must be received no later than May 10,
2007.
ADDRESSES: Comments on the application should be addressed to Michael
Payne, Chief, Permits, Conservation and Education Division, Office of
Protected Resources, National Marine Fisheries Service, 1315 East-West
Highway, Silver Spring, MD 20910-3225. The mailbox address for
providing email comments is PR1.040307B@noaa.gov. NMFS is not
responsible for e-mail comments sent to addresses other than the one
provided here. Comments sent via e-mail, including all attachments,
must not exceed a 10-megabyte file size.
A copy of the application containing a list of the references used
in this document may be obtained by writing to the address specified
above, telephoning the contact listed below (see FOR FURTHER
INFORMATION CONTACT), or visiting the internet at: https://
www.nmfs.noaa.gov/pr/permits/incidental.htm#applications.
Documents cited in this notice may be viewed, by appointment,
during regular business hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT: Jolie Harrison, Office of Protected
Resources, NMFS, (301) 713-2289, ext 166.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the MMPA (16 U.S.C. 1361 et seq.)
direct the Secretary of Commerce to allow, upon request, the
incidental, but not intentional, taking of marine mammals by U.S.
citizens who engage in a specified activity (other than commercial
fishing) within a specified geographical region if certain findings are
made and either regulations are issued or, if the taking is limited to
harassment, a notice of a proposed authorization is provided to the
public for review.
Authorization 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.
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].
Section 101(a)(5)(D) establishes a 45-day time limit for NMFS
review of an application followed by a 30-day public notice and comment
period on any proposed authorizations for the incidental harassment of
marine mammals. Within 45 days of the close of the comment period, NMFS
must either approve or deny the authorization.
Summary of Request
On January 5, 2007, NMFS received an application from SIO for the
taking, by Level B harassment only, of 32 species of marine mammals
incidental to conducting, with research funding from the National
Science Foundation (NSF), a low-energy marine seismic survey in the
northeastern Indian Ocean from May-August 2007. The purpose of the
research program is to conduct a scientific rock-dredging, magnetic,
bathymetric, and seismic survey program at nine sites on the Ninety
East Ridge in the northeastern Indian Ocean. The results will be used
to (1) determine the morphology, structure, and tectonics of ridge
volcanoes to see whether they reflect centralized (plume) or
distributed (crack) eruptions; (2) infer the magmatic evolution of the
ridge, whether it fits the plume hypothesis, and its connection to
existing hotspots; (3) examine the duration of volcanism at the various
sites and along the ridge to see whether the age progression fits the
simple plume model; and (4) survey broad characteristics of subseafloor
in
[[Page 17850]]
order to refine the planning of the IODP drilling proposal. Included in
the research planned for 2007 are scientific rock dredging at all nine
sites, high-resolution seismic methods to image the subsea floor at
five of the sites, and the use of a magnetometer, gravimeter, multi-
beam sonar, and sub-bottom profiler throughout the cruise.
Description of the Activity
The seismic surveys will involve one vessel, the R/V Roger Revelle
(Roger Revelle), which is scheduled to depart from Fremantle,
Australia, between May 22 and June 19, 2007. The Roger Revelle will
conduct the cruise in the Indian Ocean and arrive at Colombo, Sri
Lanka, between July 16 and August 13, 2007. The exact dates of the
activities may vary by a few days because of weather conditions,
repositioning, streamer operations and adjustments, airgun deployment,
or the need to repeat some lines if data quality is substandard.
Additional seismic operations may be occasionally needed to investigate
significant new findings as revealed by the other survey systems. The
overall area within which the seismic surveys will occur is located
between approximately 5[deg] N. and 25[deg] S., along approximately 90o
E. (Figure 1 in the application), in the Indian Ocean. The surveys will
be conducted entirely in International Waters.
The Roger Revelle will deploy a pair of low-energy Generator-
Injector (GI) airguns as an energy source (each with a discharge volume
of 45 in\3\), plus a 800 m-long (2625-ft long), 48-channel, towed
hydrophone. The program will consist of approximately 2700 km (1678 mi)
of surveys, including turns. Water depths within the seismic survey
areas are 1600-5100 m (1750-5577 yd). The GI guns will be operated on a
small grid for approximately 49 hours at each of 5 sites over a
approximately 50-day period during May-August 2007, commencing between
May 22 and June 19. There will be additional seismic operations
associated with equipment testing, start-up, and repeat coverage of any
areas where initial data quality is sub-standard.
In addition to the operations of the GI guns, a 3.5-kHz sub-bottom
profiler , a Kongsberg-Simrad EM-120 multi-beam sonar, and a gravimeter
will be used continuously throughout the cruise, and passive
geophysical sensors will be deployed to conduct magnetic surveys at all
times except during dredging.
Vessel Specifications
The Roger Revelle has a length of 83 m (272 ft), a beam of 16 m (52
ft), and a maximum draft of 5.2 m. The ship is powered by two 3,000 hp
Propulsion General Electric motors and an 1180-hp Azimuthing jet bow
thruster. An operation speed of 11.1 km/h (6 knots) is used during
seismic acquisition. When not towing seismic survey gear, the Roger
Revelle cruises at 22.2-23.1 km/h (12-12.5 knots) and has a maximum
speed of 27.8 km/h (15 knots). It has a normal operating range of
approximately 27,780 km (17,262 mi).
Acoustic Source Specifications
Seismic Airguns
The vessel Roger Revelle will tow a pair of GI airguns and an 800
m-long (2624-ft), 48-channel hydrophone streamer. Seismic pulses will
be emitted at intervals of 6-10 seconds, which corresponds to a shot
interval of approximatley 18.5-31 m (61-102 ft) (at a speed of 6 knots
(11.1 km/h). The generator chamber of each GI gun, the one responsible
for introducing the sound pulse into the ocean, is 45 in\3\ (total air
discharge approximately 90 in\3\). The larger (105 in\3\) injector
chamber injects air into the previously-generated bubble to maintain
its shape, and does not introduce more sound into the water. The two 45
in\3\ GI guns will be towed 8 m (26 ft) apart side by side, 21 m (69
ft) behind the Roger Revelle, at a depth of 2 m (6.6 ft). The dominant
frequency components are 0-188 Hz.
The sound pressure field of that GI gun variation has not been
modeled, but that for two 45 in\3\ Nucleus G guns (which actually have
more energy than GI guns of the same size) has been modeled by the
Lamont-Doherty Earth Observatory (L-DEO) in relation to distance and
direction from the airguns. This source, which is directed downward,
was found to have an output (0-peak) of 230.6 dB re 1 microPa m. The
nominal downward-directed source levels indicated above 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
from a hypothetical point source emitting the same total amount of
sound as is emitted by the combined GI guns. The actual received level
at any location in the water near the GI guns will not exceed the
source level of the strongest individual source. In this case, that
will be about 224.6 dB re 1 microPa-m peak, or 229.8 dB re 1 microPa-m
peak-to-peak. Actual levels experienced by any organism more than 1 m
from either GI gun will be significantly lower.
A further consideration is that the rms (root mean square) received
levels that are used as impact criteria for marine mammals are not
directly comparable to the peak or peak to peak values normally used to
characterize source levels of airgun arrays. The measurement units used
to describe airgun sources, peak or peak-to-peak decibels, are always
higher than the ``root mean square'' (rms) decibels referred to in
biological literature. A measured received level of 160 dB rms in the
far field would typically correspond to a peak measurement of
approximately 170 to 172 dB, and to a peak-to-peak measurement of
approximately 176 to 178 dB, as measured for the same pulse received at
the same location (Greene 1997; McCauley et al., 1998, 2000). The
precise difference between rms and peak or peak-to-peak values depends
on the frequency content and duration of the pulse, among other
factors. However, the rms level is always lower than the peak or peak-
to-peak level for an airgun-type source.
Bathymetric Sonar
The Roger Revelle will utilize the Kongsberg-Simrad EM120 multi-
beam sonar, which operates at 11.25-12.6 kHz and is mounted in the
hull. It operates in several modes, depending on water depth. In the
proposed survey, it will be used in deep (>800-m (2625 ft)) water, and
will operate in ``Deep'' mode. The beam width is 1[deg] or 2[deg] fore-
aft and a total of 150[deg] athwartship. Estimated maximum source
levels are 239 and 233 dB at 1[deg] and 2[deg] beam widths,
respectively. Each ``ping'' consists of nine successive fan-shaped
transmissions, each ensonifying a sector that extends 1[deg] or 2[deg]
fore-aft. In the ``Deep'' mode, the total duration of the transmission
into each sector is 15 ms. The nine successive transmissions span an
overall cross-track angular extent of about 150 degrees, with 16 ms
gaps between the pulses for successive sectors. A receiver in the
overlap area between two sectors would receive two 15-ms pulses
separated by a 16-ms gap. The ``ping'' interval varies with water
depth, from approximately 5 s at 1000 m (3280 ft) to 20 s at 4000 m
(13120 ft).
Sub-bottom Profiler
The Roger Revelle will utilize the Knudsen Engineering Model 320BR
sub-bottom profiler, which is a dual-frequency transceiver designed to
operate at 3.5 and/or 12 kHz. It is used in conjunction with the multi-
beam sonar to provide data about the sedimentary features that occur
below the sea floor. The energy from the sub-bottom profiler is
directed downward (in an 80-degree cone) via a 3.5-kHz transducer array
mounted in the hull. The maximum power output of the
[[Page 17851]]
320BR is 10 kilowatts for the 3.5-kHz section and 2 kilowatts for the
12-kHz section. (The 12-kHz section is seldom used in survey mode on
Roger Revelle because of overlap with the operating frequency of the
Kongsberg Simrad EM-120 multi-beam sonar.)
The pulse length for the 3.5 kHz section of the 320BR is 0.8-24 ms,
controlled by the system operator in regards to water depth and
reflectivity of the bottom sediments, and will usually be 12 or 24 ms
in this survey. The system produces one sound pulse and then waits for
its return before transmitting again. Thus, the pulse interval is
directly dependent upon water depth, and in this survey is 4.5-8 sec.
Using the Sonar Equations and assuming 100 percent efficiency in the
system (impractical in real world applications), the source level for
the 320BR is calculated to be 211 dB re 1 microPa-m. In practice, the
system is rarely operated above 80 percent power level.
Safety Radii
NMFS has determined that for acoustic effects, using acoustic
thresholds in combination with corresponding safety radii is the most
effective way to consistently apply measures to avoid or minimize the
impacts of an action, and to quantitatively estimate the effects of an
action. Thresholds are used in two ways: (1) to establish a mitigation
shut-down or power down zone, i.e., if an animal enters an area
calculated to be ensonified above the level of an established
threshold, a sound source is powered down or shut down; and (2) to
calculate take, in that a model may be used to calculate the area
around the sound source that will be ensonified to that level or above,
then, based on the estimated density of animals and the distance that
the sound source moves, NMFS can estimate the number of marine mammals
that may be ``taken''. NMFS believes that to avoid permanent
physiological damage (Level A Harassment), cetaceans and pinnipeds
should not be exposed to pulsed underwater noise at received levels
exceeding, respectively, 180 and 190 dB re 1 microPa (rms). NMFS also
assumes that cetaceans or pinnipeds exposed to levels exceeding 160 dB
re 1 microPa (rms) may experience Level B Harassment.
Received sound levels have been modeled by L-DEO for a number of
airgun configurations, including two 45-in\3\ Nucleus G-guns, in
relation to distance and direction from the airguns. 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 guns where sound levels of 190, 180, and 160 dB re 1 microPa
(rms) are predicted to be received in deep (>1000-m (3280-ft)) water
are 10, 40, and 400 m (33, 131, and 1312 ft), respectively. Because the
model results are for G guns, which have more energy than GI guns of
the same size, those distances are overestimates of the distances for
the 45-in\3\ GI guns.
Empirical data concerning the 180- and 160- dB distances have been
acquired based on measurements during the acoustic verification study
conducted by L-DEO in the northern Gulf of Mexico from 27 May to 3 June
2003 (Tolstoy et al., 2004). Although the results are limited, the data
showed that radii around the airguns where the received level would be
180 dB re 1 microPa (rms) vary with water depth. Similar depth-related
variation is likely in the 190-dB distances applicable to pinnipeds.
Correction factors were developed for water depths 100-1000 m (328-3280
ft) and <100 m (328 ft). The proposed survey will occur in depths 1600-
5100 m (5249-16732 ft), so the correction factors are not relevant
here.
The empirical data indicate that, for deep water (>1000 m (3280
ft)), the L-DEO model tends to overestimate the received sound levels
at a given distance (Tolstoy et al., 2004). However, to be
precautionary pending acquisition of additional empirical data, it is
proposed that safety radii during airgun operations in deep water will
be the values predicted by L-DEO's model (above). Therefore, the
assumed 180- and 190-dB radii are 40 m and 10 m (131 and 33 ft),
respectively.
Airguns will be shut down immediately when cetaceans or pinnipeds
are detected within or about to enter the appropriate 180-dB (rms) or
190-dB (rms) radius, respectively.
Description of Marine Mammals in the Activity Area
Thirty-two species of cetacean, including 25 odontocete (dolphins
and small and large toothed whales) species and seven mysticete (baleen
whales) species, are thought to occur in the proposed seismic survey
areas along the Ninety East Ridge in the northeastern Indian Ocean
(Table 1). Several are listed under the U.S. Endangered Species Act
(ESA) as Endangered: the sperm whale, humpback whale, blue whale, fin
whale, and sei whale.
Although there have been several surveys of marine mammals in the
Indian Ocean (e.g., Keller et al., 1982; Leatherwood et al., 1984; Eyre
1995; Baldwin et al., 1998; de Boer 2000; de Boer et al., 2003), data
on the occurrence, distribution, and abundance of odontocetes and
mysticetes in the northeastern Indian Ocean, encompassing the proposed
seismic survey area along the Ninety East Ridge, are limited or
lacking. Commercial whaling severely depleted all the large whale
populations in this region, and subsequently, in 1979, the
International Whaling Commission declared the Indian Ocean north of
55[deg] S. latitude a whale sanctuary. The majority of recent detailed
information on whales within the Indian Ocean Sanctuary (IOS) comes
from
(1) A United Nations Environment Programme (UNEP) Report
summarizing cetacean research in the western IOS (Leatherwood and
Donovan 1991);
(2) A compilation of sightings for the entire IOS produced by the
Whale and Dolphin Conservation Society (de Boer et al., 2003); and
(3) A review of marine mammals records in India (Sathasivam 2004);
and
(4) A series of research cruises within the IOS (Keller et al.,
1982; Leatherwood et al., 1984; Corbett 1994; Eyre 1995; Ballance and
Pitman 1998; de Boer 2000).
Because the proposed survey area spans such a wide range of
latitudes (approximately 5[deg] N.-25[deg] S.), tropical and temperate
species are found there. The survey area is all in deep-water habitat
but is close to oceanic island habitats (i.e., Andaman, Nicobar, and
Cocos (Keeling) Islands), so both coastal and oceanic species might be
encountered, although species that stay in very shallow water (e.g.,
Indian hump-backed dolphin, Irrawaddy dolphin, and finless porpoise)
would not. Abundance and density estimates of cetaceans found in areas
other than the northeastern and central Indian Ocean are provided for
reference only, and are not necessarily the same as those in the survey
area. Table 1 also shows the estimated abundance of the marine mammals
likely to be encountered during the Roger Revelle's cruise. Additional
information regarding the distribution of these species and how the
estimated densities were calculated may be found in SIO's application.
[[Page 17852]]
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Species Habitat Occurrence Rqstd Take
----------------------------------------------------------------------------------------------------------------
Mysticetes
Humpback whale (Megaptera Mainly nearshore waters Common 5(0)**
novaeangliae)* and banks
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Minke whale (Balaenoptera Pelagic and coastal Uncommon 5
acutorostrata)
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Antarctic minke whale (Balaenoptera Coastal and oceanic Uncommon 5
bonaerensis)
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Bryde's whale (Balaenoptera edeni) Pelagic and coastal Very common 5
----------------------------------------------------------------------------------------------------------------
Sei whale (Balaenoptera borealis) * Primarily offshore, Uncommon 5(0)**
pelagic
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Fin whale (Balaenoptera physalus)* Continental slope, mostly Common 5(0)**
pelagic
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Blue whale (Balaenoptera musculus)* Pelagic and coastal Very common 5(1)**
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Odontocetes
Sperm whale (Physeter macrocephalus)* Usually pelagic and deep Common 5(1)**
seas
----------------------------------------------------------------------------------------------------------------
Pygmy sperm whale (Kogia breviceps) Deep waters off the shelf Common 5
----------------------------------------------------------------------------------------------------------------
Dwarf sperm whale (Kogia sima) Deep waters off the shelf Common 5
----------------------------------------------------------------------------------------------------------------
Cuvier's beaked whale (Ziphius Pelagic Common 5
cavirostris)
----------------------------------------------------------------------------------------------------------------
Shepherd's beaked whale (Tasmacetus Pelagic Rare 5
shepherdi))
----------------------------------------------------------------------------------------------------------------
Longman's beaked whale (Indopacetus Pelagic Common? 1
pacificus)
----------------------------------------------------------------------------------------------------------------
Southern bottlenose whale (Hyperoodon Pelagic Uncommon 5
planifrons)
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True's beaked whale (Mesoplodon mirus) Pelagic Rare 5
----------------------------------------------------------------------------------------------------------------
Gray's beaked whale (Mesoplodon grayi) Pelagic Uncommon 5
----------------------------------------------------------------------------------------------------------------
Ginkgo-toothed whale (Mesoplodon Pelagic Common 5
ginkgodens)
----------------------------------------------------------------------------------------------------------------
Blainville's beaked whale (Mesoplodon Pelagic Very common 5
densirostris)
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Rough-toothed dolphin (Steno Deep water Uncommon 69
bredanensis)
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Bottlenose dolphin (Tursiops Coastal and oceanic, Common 129
truncatus) shelf break
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Pantropical spotted dolphin (Stenella Coastal and pelagic Uncommon 65
attenuata)
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Spinner dolphin (Stenella Coastal and pelagic Abundant 215
longirostris)
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Striped dolphin (Stenella Off continental shelf Common 86
coeruleoalba)
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Fraser's dolphin (Lagenodelphis hosei) Waters >1000 m Rare 22
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Common dolphin (Delphinus delphis) Shelf and pelagic, Very common 151
seamounts
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Risso's dolphin (Grampus griseus) Waters >1000 m, seamounts Very common 151
----------------------------------------------------------------------------------------------------------------
Melon-headed whale (Peponocephala Oceanic Very common 50
electra)
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Pygmy killer whale (Feresa attenuata) Deep, pantropical waters Common 25
----------------------------------------------------------------------------------------------------------------
False killer whale (Pseudorca Pelagic Common 15
crassidens)
----------------------------------------------------------------------------------------------------------------
Killer whale (Orcinus orca) Widely distributed Common 5
----------------------------------------------------------------------------------------------------------------
Long-finned pilot whale (Globicephala Mostly pelagic Rare 30
melas)
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[[Page 17853]]
Short-finned pilot whale (Globicephala Mostly pelagic, high- Very common 15
macrorhynchus) relief topography
----------------------------------------------------------------------------------------------------------------
Table 1. Species expected to be encountered (and potentially harassed) during SIO's Indian Ocean cruise
*Species are listed as endangered under the Endangered Species Act
**Parenthetical numbers represent numbers of takes NMFS proposes to authorize (we may not authorize take
ofspecies, or take of numbers of species, that we are not exempted pursuant to our internal ESA consultation)
Potential Effects on Marine Mammals
Potential Effects of Airguns
The effects of sounds from airguns might include one or more of the
following: tolerance, masking of natural sounds, behavioral
disturbance, and temporary or permanent hearing impairment (Richardson
et al., 1995). Given the small size of the GI guns planned for the
present project, effects are anticipated to be considerably less than
would be the case with a large array of airguns. It is very unlikely
that there would be any cases of temporary or, especially, permanent
hearing impairment. Also, behavioral disturbance is expected to be
limited to relatively short distances.
Tolerance
Numerous studies have shown that pulsed sounds from airguns are
often readily detectable in the water at distances of many kilometers.
For a summary of the characteristics of airgun pulses, see Appendix A
of SIO's application. However, it should be noted that most of the
measurements of airgun sounds that have been reported concerned sounds
from larger arrays of airguns, whose sounds would be detectable
considerably farther away than the GI guns planned for use in the
present project.
Numerous studies have shown that marine mammals at distances more
than a few kilometers from operating seismic vessels often show no
apparent response-see Appendix A (e) of SIO's application. That is
often true even in cases when the pulsed sounds must be readily audible
to the animals based on measured received levels and the hearing
sensitivity of that mammal group. Although various baleen whales,
toothed whales, and (less frequently) pinnipeds have been shown to
react behaviorally to airgun pulses under some conditions, at other
times mammals of all three types have shown no overt reactions. In
general, pinnipeds and small odontocetes seem to be more tolerant of
exposure to airgun pulses than are baleen whales. Given the relatively
small and low-energy airgun source planned for use in this project,
mammals (and sea turtles) are expected to tolerate being closer to this
source than might be the case for a larger airgun source typical of
most seismic surveys.
Masking
Masking effects of pulsed sounds (even from large arrays of
airguns) on marine mammal calls and other natural sounds are expected
to be limited, although there are very few specific data on this. Some
whales are known to continue calling in the presence of seismic pulses.
Their calls can be heard between the seismic pulses (e.g., Richardson
et al., 1986; McDonald et al., 1995; Greene et al., 1999; Nieukirk et
al., 2004). Although there has been one report that sperm whales cease
calling when exposed to pulses from a very distant seismic ship (Bowles
et al., 1994), a recent study reports that sperm whales off northern
Norway continued calling in the presence of seismic pulses (Madsen et
al., 2002c). That has also been shown during recent work in the Gulf of
Mexico (Tyack et al., 2003). Given the small source planned for use
here, there is even less potential for masking of baleen or sperm whale
calls during the present study than in most seismic surveys. Masking
effects of seismic pulses are expected to be negligible in the case of
the smaller odontocete cetaceans, given the intermittent nature of
seismic pulses and the relatively low source level of the airguns to be
used here. Also, the sounds important to small odontocetes are
predominantly at much higher frequencies than are airgun sounds.
Masking effects, in general, are discussed further in Appendix A (d) of
SIO's application.
Disturbance Reactions
Disturbance includes a variety of effects, including subtle changes
in behavior, more conspicuous changes in activities, and displacement.
Disturbance is one of the main concerns in this project. Reactions to
sound, if any, depend on species, state of maturity, experience,
current activity, reproductive state, time of day, and many other
factors. If a marine mammal responds to an underwater sound by changing
its behavior or moving a small distance, the response may or may not
rise to the level of harassment, let alone affect the stock or the
species as a whole. Alternatively, if a sound source displaces marine
mammals from an important feeding or breeding area, effects on the
stock or species could potentially be more than negligible. 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 are likely to be present within a particular distance of
industrial activities, or exposed to a particular level of industrial
sound. This practice potentially overestimates the numbers of marine
mammals that are affected in some biologically important manner.
The sound criteria used to estimate how many marine mammals might
be disturbed to some biologically-important degree by a seismic program
are based on behavioral observations during studies of several species.
However, information is lacking for many species. Detailed studies have
been done on humpback, gray, and bowhead whales, and on ringed seals.
Less detailed data are available for some other species of baleen
whales, sperm whales, and small toothed whales. Most of those studies
have focused on the impacts resulting from the use of much larger
airgun sources than those planned for use in the present project. Thus,
effects are expected to be limited to considerably smaller distances
and shorter periods of exposure in the present project than in most of
the previous work concerning marine mammal reactions to airguns.
Baleen Whales - Baleen whales generally tend to avoid operating
airguns, but avoidance radii are quite variable. Whales are often
reported to show no overt reactions to pulses from large arrays of
airguns at distances beyond a few kilometers, even though the airgun
pulses remain well above ambient noise levels out to much longer
distances. However, as reviewed in Appendix A (e) of SIO's application,
baleen whales exposed to strong noise pulses from airguns often react
by deviating from their normal migration route and/or interrupting
their feeding activities and moving away from the sound source. In the
case of the migrating gray and bowhead whales, the observed changes in
behavior appeared
[[Page 17854]]
to be of little or no biological consequence to the animals. They
simply avoided the sound source by displacing their migration route to
varying degrees, but within the natural boundaries of the migration
corridors.
Studies of gray, bowhead, and humpback whales have determined that
received levels of pulses in the 160-170 dB re 1 microPa rms range seem
to cause obvious avoidance behavior in a substantial fraction of the
animals exposed. In many areas, seismic pulses from large arrays of
airguns diminish to those levels at distances ranging from 4.5-14.5 km
(2.8-9 mi) from the source. A substantial proportion of the baleen
whales within those distances may show avoidance or other strong
disturbance reactions to the airgun array. Subtle behavioral changes
sometimes become evident at somewhat lower received levels, and recent
studies, reviewed in Appendix A (e) of SIO's application, have shown
that some species of baleen whales, notably bowheads and humpbacks, at
times show strong avoidance at received levels lower than 160-170 dB re
1 microPa rms. Reaction distances would be considerably smaller during
the present project, in which the 160-dB radius is predicted to be
approximately 0.40 km (0.9 mi), as compared with several kilometers
when a large array of airguns is operating.
Humpback whales summering 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 150-169 dB re 1 microPa on an approximate rms
basis. Malme et al. (1985) concluded that there was no clear evidence
of avoidance, despite the possibility of subtle effects, at received
levels up to 172 re 1 microPa (approximately rms). More detailed
information on responses of humpback whales to seismic pulses during
studies in Australia can be found in Appendix A (a) of SIO's
application.
Malme et al. (1986, 1988) studied the responses of feeding eastern
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 ceased feeding at
an average received pressure level of 173 dB re 1 microPa on an
(approximate) rms basis, and that 10 percent of feeding whales
interrupted feeding at received levels of 163 dB. Those findings were
generally consistent with the results of experiments conducted on
larger numbers of gray whales that were migrating along the California
coast.
Data on short-term reactions (or lack of reactions) of cetaceans to
impulsive noises do not necessarily provide information about long-term
effects. It is not known whether impulsive noises affect reproductive
rate or distribution and habitat use in subsequent days or years.
However, gray whales continued to migrate annually along the west coast
of North America despite intermittent seismic exploration and much ship
traffic in that area for decades (Appendix A in Malme et al., 1984).
Bowhead whales continued to travel to the eastern Beaufort Sea each
summer despite seismic exploration in their summer and autumn range for
many years (Richardson et al., 1987). In any event, the brief exposures
to sound pulses from the present small airgun source are highly
unlikely to result in prolonged effects.
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, systematic work on sperm
whales is underway (Tyack et al., 2003).
Seismic operators sometimes see dolphins and other small toothed
whales near operating airgun arrays, but in general there seems to be a
tendency for most delphinids to show some limited avoidance of seismic
vessels operating large airgun systems. However, some dolphins seem to
be attracted to the seismic vessel and floats, and some ride the bow
wave of the seismic vessel even when large arrays of airguns are
firing. Nonetheless, there have been indications that small toothed
whales sometimes 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., Goold, 1996; Calambokidis and Osmek,
1998; Stone, 2003). Similarly, captive bottlenose dolphins and beluga
whales exhibit changes in behavior when exposed to strong pulsed sounds
similar in duration to those typically used in seismic surveys
(Finneran et al., 2000, 2002). However, the animals tolerated high
received levels of sound (pk-pk level >200 dB re 1 microPa) before
exhibiting aversive behaviors. With the presently-planned small airgun
system, such levels would only be found within a few meters of the
airguns.
There are no specific data on the behavioral reactions of beaked
whales to seismic surveys. A few beaked whale sightings have been
reported from seismic vessels (Stone, 2003), however, based on limited
observations most beaked whales tend to avoid approaching vessels of
other types (e.g., Kasuya, 1986; Wursig et al., 1998). Several beaked
whale strandings have been associated with naval mid-frequency sonar
exercises, however, the sounds produced by seismic airguns are quite
different from tactical sonar (see Appendix A (g) of SIO's
application). The strandings mentioned above are apparently at least in
part a disturbance response, although auditory or other injuries may
also be a factor. Whether beaked whales would ever react similarly to
seismic surveys is unknown (see ``Strandings and Mortality'', below).
Sperm whales have been reported to show avoidance reactions to
standard vessels not emitting airgun sounds, and it is to be expected
that they would tend to avoid an operating seismic survey vessel. There
were some limited early observations suggesting that sperm whales in
the Southern Ocean and Gulf of Mexico might be fairly sensitive to
airgun sounds from distant seismic surveys. However, more extensive
data from recent studies in the North Atlantic suggest that sperm
whales in those areas show little evidence of avoidance or behavioral
disruption in the presence of operating seismic vessels (McCall Howard,
1999; Madsen et al., 2002c; Stone, 2003).
Odontocete reactions to large arrays of airguns are variable and,
at least for small odontocetes, seem to be confined to a smaller radius
than has been observed for mysticetes. Thus, behavioral reactions of
odontocetes to the small airgun source to be used here are expected to
be very localized, probably to distances <0.40 km (.25 mi).
Pinnipeds - Pinnipeds are not likely to show a strong avoidance
reaction to the small airgun source that will be used. Visual
monitoring from seismic vessels, usually employing larger sources, has
shown only slight (if any) avoidance of airguns by pinnipeds, and only
slight (if any) changes in behavior-see Appendix A (e) of SIO's
application. Those studies show that pinnipeds frequently do not avoid
the area within a few hundred meters of operating airgun arrays, even
for arrays much larger than the one to be used here (e.g., Harris et
al., 2001). However, initial telemetry work suggests that avoidance and
other behavioral reactions to small airgun sources may be stronger than
evident to date from visual studies of pinniped reactions to airguns
(Thompson et al., 1998). Even if reactions of the species occurring in
the present study area are as strong as those evident in the telemetry
study, reactions are expected to be confined to relatively
[[Page 17855]]
small distances and durations, with no long-term effects on pinnipeds.
Additional details on the behavioral reactions (or the lack
thereof) by all types of marine mammals to seismic vessels can be found
in Appendix A (e) of SIO's application.
Hearing Impairment and Other Physical Effects
Temporary or permanent hearing impairment is a possibility when
marine mammals are exposed to very strong sounds, but there has been no
specific documentation of this for marine mammals exposed to sequences
of airgun pulses. Current NMFS policy regarding exposure of marine
mammals to high-level sounds is that cetaceans and pinnipeds should not
be exposed to impulsive sounds of 180 and 190 dB re 1 microPa (rms),
respectively. Those criteria have been used in defining the safety
(shut-down) radii planned for the proposed seismic survey. The
precautionary nature of these criteria is discussed in Appendix A (f)
of SIO's application, including the fact that the minimum sound level
necessary to cause permanent hearing impairment is higher, by a
variable and generally unknown amount, than the level that induces
barely-detectable temporary threshold shift (TTS) (which NMFS' criteria
are based on) and the level associated with the onset of TTS is often
considered to be a level below which there is no danger of permanent
damage. NMFS is presently developing new noise exposure criteria for
marine mammals that take account of the now-available data on TTS in
marine (and terrestrial) mammals.
Because of the small size of the airgun source in this project (two
45-in\3\ GI guns), along with the planned monitoring and mitigation
measures, there is little likelihood that any marine mammals will be
exposed to sounds sufficiently strong to cause hearing impairment.
Several aspects of the planned monitoring and mitigation measures for
this project are designed to detect marine mammals occurring near the
two GI airguns (and multi-beam bathymetric sonar), and to avoid
exposing them to sound pulses that might, at least in theory, cause
hearing impairment. In addition, many cetaceans are likely to show some
avoidance of the area with high received levels of airgun sound (see
above). In those cases, the avoidance responses of the animals
themselves will reduce or (most likely) avoid any possibility of
hearing impairment.
Non-auditory physical effects may also occur in marine mammals
exposed to strong underwater pulsed sound. Possible types of non-
auditory physiological effects or injuries that theoretically might
occur in mammals close to a strong sound source include stress,
neurological effects, bubble formation, resonance effects, and other
types of organ or tissue damage. It is possible that some marine mammal
species (i.e., beaked whales) may be especially susceptible to injury
and/or stranding when exposed to strong pulsed sounds. However, as
discussed below, there is no definitive evidence that any of these
effects occur even for marine mammals in close proximity to large
arrays of airguns. It is especially unlikely that any effects of these
types would occur during the present project given the small size of
the source, the brief duration of exposure of any given mammal, and the
planned monitoring and mitigation measures (see below). The following
subsections discuss in somewhat more detail the possibilities of TTS,
permanent threshold shift (PTS), and non-auditory physical effects.
Temporary Threshold Shift (TTS) - 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. 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 recovers
rapidly after exposure to the noise ends. Only a 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.
For toothed whales exposed to single short pulses, the TTS
threshold appears to be, to a first approximation, a function of the
energy content of the pulse (Finneran et al., 2002). Given the
available data, the received level of a single seismic pulse might need
to be approximately 210 dB re 1 microPa rms (approximately 221-226 dB
pk-pk) in order to produce brief, mild TTS. Exposure to several seismic
pulses at received levels near 200-205 dB (rms) might result in slight
TTS in a small odontocete, assuming the TTS threshold is (to a first
approximation) a function of the total received pulse energy. Seismic
pulses with received levels of 200-205 dB or more are usually
restricted to a radius of no more than 100 m (328 ft) around a seismic
vessel operating a large array of airguns. Such levels would be limited
to distances within a few meters of the small GI-gun source to be used
in this project.
For baleen whales, there are no data, direct or indirect, on levels
or properties of sound that are required to induce TTS. However, no
cases of TTS are expected given the small size of the source, and, as
mentioned previously, there is a strong likelihood that baleen whales
would avoid the approaching GI gun (or vessel), with the sound source
operating, before being exposed to levels high enough for there to be
any possibility of TTS.
In pinnipeds, TTS thresholds associated with exposure to brief
pulses (single or multiple) of underwater sound have not been measured.
Initial evidence from prolonged exposures suggested that some pinnipeds
may incur TTS at somewhat lower received levels than do small
odontocetes exposed for similar durations (Kastak et al., 1999; Ketten
et al., 2001; cf. Au et al., 2000). However, more recent indications
are that TTS onset in the most sensitive pinniped species studied
(harbor seal) may occur at a similar sound exposure level as in
odontocetes (Kastak et al., 2004).
A marine mammal within a radius of 100 m (328 ft) around a typical
large array of operating airguns might be exposed to a few seismic
pulses with levels of 205 dB, and possibly more pulses if the mammal
moved with the seismic vessel. (As noted above, most cetacean species
tend to avoid operating airguns, although not all individuals do so.)
In addition, ramping up airgun arrays, which is standard operational
protocol for large airgun arrays, provides an opportunity for cetaceans
to move away from the seismic source and to avoid being exposed to the
full acoustic output of the airgun array. However, several of the
considerations that are relevant in assessing the impact of typical
seismic surveys with arrays of airguns are not directly applicable
here:
(1) The planned GI gun source is much smaller, with correspondingly
smaller radii within which received sound levels could exceed any
particular level of concern.
(2) With a large airgun array, it is unlikely that cetaceans would
be exposed to airgun pulses at a sufficiently high level for a
sufficiently long period to cause more than mild TTS, given the
relative movement of the vessel and the marine mammal. In this project,
the gun source is much smaller, so the radius of influence and duration
of exposure to strong pulses is much smaller, especially in deep and
intermediate-depth water.
(3) With a large array of airguns, TTS would be most likely in any
odontocetes that bow-ride or otherwise linger near the airguns. In the
present project, the
[[Page 17856]]
anticipated 180-dB distance in deep water is 40 m (131 ft), and the
waterline at the bow of the Roger Revelle will be approximately 97 m
(318 ft) ahead of the GI gun.
To avoid injury, NMFS has determined that cetaceans and pinnipeds
should not be exposed to pulsed underwater noise at received levels
exceeding, respectively, 180 and 190 dB re 1 microPa (rms). The
predicted 180- and 190-dB distances for the GI guns operated by SIO are
40 m (131 ft) and 10 m (33 ft), respectively, in water depths >1000 m
(3280 ft). [Those distances actually apply to operations with two 45-
in\3\ G guns, and smaller distances would be expected for the two 45-
in\3\ GI guns to be used here.] These sound levels are the received
levels above which, in the view of a panel of bioacoustics specialists
convened by NMFS, one cannot be certain that there will be no injurious
effects, auditory or otherwise, to marine mammals. More recent TTS data
imply that, at least for dolphins, TTS is unlikely to occur unless the
dolphins are exposed to airgun pulses notably stronger than 180 dB re 1
microPa rms. However NMFS utilizes a precautionary approach of
requiring shut down at received levels above which we cannot be certain
there will be no injurious effects to the most sensitive species.
Permanent Threshold Shift (PTS) - When PTS occurs, there is
physical damage to the sound receptors in the ear. In some cases, there
can be total or partial deafness, while in other cases, the animal has
an impaired ability to hear sounds in specific frequency ranges. 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 TTS, there has been further speculation about the
possibility that some individuals occurring very close to airguns might
incur PTS. Single or occasional occurrences of mild TTS are not
indicative of permanent auditory damage in terrestrial mammals.
Relationships between TTS and PTS thresholds have not been studied in
marine mammals, but are assumed to be similar to those in humans and
other terrestrial mammals. PTS might occur at a received sound level 20
dB or more above that inducing mild TTS if the animal were exposed to
the strong sound for an extended period, or to a strong sound with
rather rapid rise time-see Appendix A (f) of SIO's application.
It is highly unlikely that marine mammals could receive sounds
strong enough to cause permanent hearing impairment during a project
employing two 45-in\3\ GI guns. In the present project, marine mammals
are unlikely to be exposed to received levels of seismic pulses strong
enough to cause TTS, as they would probably need to be within a few
meters of the airguns for that to occur. Given the higher level of
sound necessary to cause PTS, it is even less likely that PTS could
occur. In fact, even the levels immediately adjacent to the airguns may
not be sufficient to induce PTS, especially since a mammal would not be
exposed to more than one strong pulse unless it swam immediately
alongside an airgun for a period longer than the inter-pulse interval
(6-10 s). Baleen whales generally avoid the immediate area around
operating seismic vessels. The planned monitoring and mitigation
measures, including visual monitoring, ramp ups, and shut downs of the
airguns when mammals are seen within the ``safety radii'', will
minimize the already-minimal probability of exposure of marine mammals
to sounds strong enough to induce PTS.
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 effects, and other types of organ
or tissue damage. There is no evidence that any of these effects occur
in marine mammals exposed to sound from airgun arrays (even large ones)
and there have been no direct studies of the potential for airgun
pulses to elicit any of those effects. NMFS does not anticipate that
marine mammals would experience any of these effects in response to
being exposed to the airguns in this proposed study, especially
considering the small size of the airguns. If any such effects do
occur, they would probably be limited to unusual situations when
animals might be exposed at close range for unusually long periods.
Exposure of laboratory animals, wildlife, and humans to strong
noise often results in significant increases in adrenal activity,
including cortisol and/or catecholamine release and related measures of
stress (see Appendix A of SIO's application). However, it is doubtful
that any single marine mammal would be exposed to strong seismic sounds
for sufficiently long that significant physiological stress would
develop. That is especially so in the case of the present project where
the airguns are small, the ship's speed is relatively fast (5-8 knots
or 9.3-14.8 km/h), and each survey does not encompass a large area.
Gas-filled structures in marine animals have an inherent
fundamental resonance frequency. If stimulated at that frequency, the
ensuing resonance could cause damage to the animal. A workshop (Gentry
[ed.] 2002) was held to discuss whether the stranding of beaked whales
in the Bahamas in 2000 (Balcomb and Claridge, 2001; NOAA and USN, 2001)
might have been related to air cavity resonance or bubble formation in
tissues caused by exposure to noise from naval sonar. A panel of
experts concluded that resonance in air-filled structures was not
likely to have caused this stranding. Opinions were less conclusive
about the possible role of gas (nitrogen) bubble formation/growth in
the Bahamas stranding of beaked whales.
Until recently, it was assumed that diving marine mammals are not
subject to the bends or air embolism. However, a short paper concerning
beaked whales stranded in the Canary Islands in 2002 suggests that
cetaceans might be subject to decompression injury in some situations
(Jepson et al., 2003). If so, that might occur if they ascend quickly
when exposed to aversive sounds. However, the interpretation that the
effect was related to decompression injury is unproven (Piantadosi and
Thalmann 2004; Fernandez et al., 2004). Even if that effect can occur
during exposure to mid-frequency sonar, there is no evidence that this
type of effect occurs in response to airgun sounds. It is especially
unlikely in the case of the proposed survey, involving only two GI
guns.
In general, little is known about the potential for seismic survey
sounds to cause auditory impairment or other physical effects in marine
mammals. Available data suggest that such effects, if they occur at
all, would be limited to short distances and probably to projects
involving large arrays of airguns. However, the available data do not
allow for 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 auditory impairment or other physical effects. Also,
the planned mitigation measures, including ramp ups and shut downs,
will reduce any such effects that might otherwise occur.
Strandings and Mortality
Marine mammals close to underwater detonations of high explosives
can be killed or severely injured, and their auditory organs are
especially
[[Page 17857]]
susceptible to injury (Ketten et al., 1993; Ketten 1995). Airgun pulses
are less energetic and have slower rise times, and there is no proof
that they can cause serious injury, death, or stranding even in the
case of large airgun arrays. However, the association of several
strandings of beaked whales with naval exercises and, in one case, an
L-DEO seismic survey, has raised the possibility that beaked whales
exposed to strong pulsed sounds may be especially susceptible to injury
and/or behavioral reactions that can lead to stranding. Appendix A (g)
of SIO's application provides additional details.
Seismic pulses and mid-frequency sonar pulses are quite different.
Sounds produced by airgun arrays are broadband with most of the energy
below 1 kHz. Typical military mid-frequency sonars operate at
frequencies of 2-10 kHz, generally with a relatively narrow bandwidth
at any one time. Thus, it is not appropriate to assume that there is a
direct connection between the effects of military sonar and seismic
surveys on marine mammals. However, evidence that sonar pulses can, in
special circumstances, lead to physical damage and mortality (NOAA and
USN 2001; Jepson et al., 2003), even if only indirectly, suggests that
caution is warranted when dealing with exposure of marine mammals to
any high-intensity pulsed sound.
In May 1996, 12 Cuvier's beaked whales stranded along the coasts of
Kyparissiakos Gulf in the Mediterranean Sea. That stranding was
subsequently linked to the use of low- and medium-frequency active
sonar by a North Atlantic Treaty Organization (NATO) research vessel in
the region (Frantzis 1998). In March 2000, a population of Cuvier's
beaked whales being studied in the Bahamas disappeared after a U.S.
Navy task force using mid-frequency tactical sonars passed through the
area; some beaked whales stranded (Balcomb and Claridge, 2001; NOAA and
USN, 2001).
In September 2002, a total of 14 beaked whales of various species
stranded coincident with naval exercises in the Canary Islands (Martel
n.d.; Jepson et al., 2003; Fernandez et al., 2003). Also in Sept. 2002,
there was a stranding of two Cuvier's beaked whales in the Gulf of
California, Mexico, when the L-DEO vessel Maurice Ewing was operating a
20-gun, 8490-in\3\ array in the general area. The link between the
stranding and the seismic surveys was inconclusive and not based on any
physical evidence (Hogarth, 2002; Yoder, 2002). Nonetheless, that plus
the incidents involving beaked whale strandings near naval exercises
suggests a need for caution in conducting seismic surveys in areas
occupied by beaked whales.
The present project will involve a much smaller sound source than
used in typical seismic surveys. That, along with the monitoring and
mitigation measures that are planned, are expected to minimize any
possibility for strandings and mortality.
Potential Effects of Other Acoustic Devices
Bathymetric Sonar Signals
A multi-beam bathymetric sonar (Simrad EM120, 11.25-12.6 kHz) will
be operated from the source vessel during much of the planned study.
Sounds from the multi-beam sonar are very short pulses. Most of the
energy in the sound pulses emitted by the multi-beam is at moderately
high frequencies, centered at 12 kHz. The beam is narrow (1[deg] or
2[deg]) in fore-aft extent, and wide (150[deg]) in the cross-track
extent. Each ping consists of nine successive transmissions (segments)
at different cross-track angles. Any given mammal at depth near the
track line would be in the main beam for only a fraction of a second.
Tactical Navy sonars that have been linked to avoidance reactions
and stranding of cetaceans (1) generally are more powerful than the
Simrad EM120, (2) have a longer pulse duration, and (3) are directed
close to omnidirectionally, vs. downward for the Simrad EM120. The area
of possible influence of the Simrad EM120 is a much smaller narrow band
oriented in the cross-track direction below the source vessel. Marine
mammals that encounter the Simrad EM120 at close range are unlikely to
be subjected to repeated pulses because of the narrow fore-aft width of
the beam, and will receive only limited amounts of pulse energy because
of the short pulses. In assessing the possible impacts of the 15.5 kHz
Atlas Hydrosweep (a similar model), Boebel et al. (2004) noted that the
critical sound pressure level at which TTS may occur is 203.2 dB re 1
microPa (rms). The critical region included an area of 43 m (141 ft) in
depth, 46 m (151 ft) wide athwartship, and 1 m (3.3 ft) fore-and-aft
(Boebel et al., 2004).
Behavioral reactions of free-ranging marine mammals to military and
other sonars 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. However, all of those observations are of
limited relevance to the present situation. Pulse durations from those
sonars were much longer than those of the SIO multi-beam sonar, and a
given mammal would have received many pulses from the naval sonars.
During SIO's operations, the individual pulses will be very short, and
a given mammal would not receive many of the downward-directed pulses
as the vessel passes by.
Captive bottlenose dolphins and a white whale exhibited changes in
behavior when exposed to 1 s pulsed sounds at frequencies similar to
those that will be emitted by the multi-beam sonar 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). The relevance of those
data to free-ranging odontocetes is uncertain, and in any case, the
test sounds were quite different in either duration or bandwidth as
compared with those from a bathymetric sonar.
Because of the shape of the beam, NMFS believes it unlikely that
marine mammals will be exposed to the bathymetric sonar at levels at or
above those likely to cause harassment. Further, NMFS believes that the
brief exposure of cetaceans or pinnipeds to one pulse, or small numbers
of signals, from the multi-beam bathymetric sonar system are not likely
to result in the harassment of marine mammals.
Sub-bottom Profiler Signals
A sub-bottom profiler will be operated from the source vessel at
all times during the planned study. Sounds from the sub-bottom profiler
are very short pulses, occurring for 12 or 24 ms once every 4.5-8
seconds. Most of the energy in the sound pulses emitted by this sub-
bottom profiler is at mid frequencies, centered at 3.5 kHz. The beam
width is approximately 80o (cone-shaped) and is directed downward.
The sub-bottom profiler on the Roger Revelle has a stated maximum
source level of 211 dB re 1 microPa m (see section I of SIO's
application). Thus, the received level would be expected to decrease to
180 dB and 160 dB approximately 35 m and 350 m below the transducer,
respectively, assuming spherical spreading. Corresponding distances in
the horizontal plane would be substantially lower, given the
directionality of this source.
Marine mammal behavioral reactio