Small Takes of Marine Mammals Incidental to Specified Activities; Low-Energy Marine Seismic Survey in the Northeast Pacific Ocean, June-July 2008, 30076-30093 [E8-11546]
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30076
Federal Register / Vol. 73, No. 101 / Friday, May 23, 2008 / Notices
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Dated: May 19, 2008.
Emily Menashes,
Acting Director, Office of Sustainable
Fisheries, National Marine Fisheries Service.
[FR Doc. E8–11580 Filed 5–22–08; 8:45 am]
BILLING CODE 3510–22–S
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XG64
Small Takes of Marine Mammals
Incidental to Specified Activities; LowEnergy Marine Seismic Survey in the
Northeast Pacific Ocean, June–July
2008
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 University of Texas,
Institute of Geophysics (UTIG) for an
Incidental Harassment Authorization
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(IHA) to take marine mammals
incidental to conducting a low-energy
marine seismic survey in the Northeast
Pacific Ocean during June-July, 2008.
Pursuant to the Marine Mammal
Protection Act (MMPA), NMFS is
requesting comments on its proposal to
issue an IHA to UTIG 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 June 23, 2008.
ADDRESSES: Comments on the
application should be addressed to P.
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
PR1.0648XB70@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:
Howard Goldstein or Ken Hollingshead,
Office of Protected Resources, NMFS,
(301) 713–2289.
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
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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 U.S. 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 March 4, 2008, NMFS received an
application from UTIG for the taking, by
Level B harassment only, of several
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species of marine mammals incidental
to conducting, with research funding
from the National Science Foundation
(NSF), a bathymetric and seismic survey
program approximately 100 km
(approximately 62 mi) off the Oregon
coast in the Northeast Pacific Ocean
during June-July, 2008. The purpose of
the research program is to investigate
the methane vent systems that exist
offshore Oregon. These systems release
methane by active venting at the
seafloor. They can also form relatively
high concentrations of methane hydrate
in the sub seafloor, up to 150 m (492 ft)
below the sea bottom. The goal is to
image these systems in detail to
understand how vent structure directs
methane from the subsurface to be
vented into the oceans, or potentially
stored in the subsurface as methane
hydrate. Methane is a significant
greenhouse gas, and methane release
from vents or from hydrate has a
significant potential to affect the Earth’s
climate. Hydrates are also a potentially
significant source of energy. Also
included in the research is the use of a
multibeam echosounder and sub-bottom
profiler.
Description of the Proposed Activity
The seismic survey will involve one
vessel, the R/V Thomas G. Thompson
(Thompson), which is scheduled to
depart from Seattle, Washington on June
30, 2008 and return on July 19, 2008.
The exact dates of the activities may
vary by a few days because of weather
conditions, scheduling, repositioning,
streamer operations and adjustments, GI
airguns deployment, or the need to
repeat some lines if data quality is
substandard. The proposed ultra-high
resolution 3–dimensional (3–D) seismic
surveys around the methane vent
systems of Hydrate Ridge, will take
place off the Oregon coast in the
northeastern Pacific Ocean. The overall
area within which the seismic surveys
will occur is located between
approximately 44° and 45° N. and
124.5° and 126° W (Figure 1 in the
application). The surveys will occur
approximately 100 km (approximately
62 mi) offshore from Oregon in water
depths between approximately 650 and
1,200 m (2,132 and 3,936 ft), entirely
within the Exclusive Economic Zone
(EEZ) of the U.S.
The seismic survey will image the
subsurface structures that control
venting. The vent systems control
whether the methane is directly released
into the ocean and atmosphere or stored
in methane hydrate. Methane hydrate
storage has the potential for rapid
dissociation and release into the ocean
or atmosphere. The subsurface structure
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that will be imaged will determine the
mechanisms involved in methane
venting. The results will be applicable
to the numerous vent systems that exist
on continental margins worldwide. The
data will also be used to design
observatories that can monitor and
assess the methane fluxes and
mechanisms of methane release that
operate on Hydrate Ridge.
The Thompson will deploy two lowenergy Generator-Injector (GI) airguns
(guns) as an energy source (with a
discharge volume of 40–60 in3 for each
gun or a total of 80–120 in3) , and a PCable system. The 12 m (39.5 ft) long PCable system is supplied by
Northampton Oceanographic Center in
the U.K. The towed system will consist
of at least 12 streamers (and possibly up
to 24) spaced approximately 12.5 m (41
ft) apart and each containing 11
hydrophones, all summed to a single
channel. The energy to the GI guns is
compressed air supplied by compressors
on board the source vessel. As the GI
guns are towed along the survey lines,
the P-Cable system will receive the
returning acoustic signals.
The seismic program will consist of
three survey grids: two of the surveys
each cover a 15 km2 area and the third
covers a 25 km2 (see Figure 1 in UTIG’s
application). The line spacing within
the three survey grids will either be 75
m (246 ft) (if 12 streamers are used) or
150 m (492 ft) (if 24 streamers are used).
The total line km to be surveyed in the
grids at the 75 m spacing is 975 km
(605.8 mi), including turns. Water
depths at the seismic survey locations
range from 650 to 1,200 m (2132 to 3936
ft). Most (92 percent) of the survey will
take place over intermediate (100–1,000
m) water depths; the remaining 8
percent will be in water deeper than
1,000 m. If time permits, an additional
300 line km will be surveyed along the
outside edges of the three grids. The GI
guns are expected to operate for a total
of approximately 150 hours during the
cruise. 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
two GI guns and P-cable system, a
Simrad EM300 30 kHz multibeam
echosounder, and a Knudsen 12 kHz
320BR sub-bottom profiler will be used
during the proposed cruise.
Vessel Specifications
The Thompson has a length of 83.5 m
(274 ft), a beam of 16 m (52.5 ft), and
a maximum draft of 5.8 m (19 ft). The
ship is powered by twin 360°-azimuth
stern thrusters a single 3,000–hp DC
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30077
motor and a water-jet bow thruster
powered by a 1,600–hp motor. The
motors are driven by up to three 1,500–
kW and three 715–kW generators;
normal operations use two 1,500–kW
and one 750–kW generator, but this
changes with ship speed, sea state, and
other variables. An operation speed of
6.5 km/h (3.5 knots) will be used during
seismic acquisition. When not towing
seismic survey gear, the Thompson
cruises at 22.2 km/h (12 knots) and has
a maximum speed of 26.9 km/h (14.5
knots). It has a normal operating range
of approximately 24,400 km (8,264 mi).
Acoustic Source Specifications
Seismic Airguns
The vessel Thompson will tow two GI
guns and a P-Cable system of 12 to 24,
12 m long streamers containing
hydrophones along predetermined
survey grids. Seismic pulses will be
emitted at intervals of 3.5 s, which
corresponds to a shot interval of
approximately 6.3 m (20.7 ft) at a speed
of 3.5 knots (6.5 km/h). The generator
chamber of a GI gun, the one
responsible for introducing the sound
pulse into the ocean, is 40–60 in3. The
second injector chamber (40–60 in3)
injects air into the previously-generated
bubble to maintain its shape and does
not introduce more sound into the
water. The two 40–60 in3 GI guns will
be towed 29 m (95.1 ft) behind the
Thompson, at a depth of 1.5–3 m (4.9–
9.8 ft). The dominant frequency
components are 0–188 Hz.
The sound pressure field of two 105
in3 GI guns has been modeled by the
Lamont-Doherty Earth Observatory (LDEO) of Columbia University in relation
to distance and direction from the GI
guns. The model does not allow for
bottom interactions and is most directly
applicable to close distances and/or
deep water. Because the L-DEO model is
for a pair of larger GI guns with a total
discharge of up to 210 in3, the values
overestimate the distances for two GI
guns with a discharge of up to 120 in3,
as planned for use during the proposed
study. This source, which is directed
downward, was found to have an output
(0–peak) of 237 dB re 1 µPam.
The root mean square (rms) 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 rms
decibels referred to in biological
literature. A measured received level of
160 dB rms in the far field would
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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.
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Sub-bottom Profiler
The Thompson will utilize a Simrad
EM300 30–kHz Multibeam Echosounder
(MBES) as the primary bottom-mapping
echosounder during the cruise. The
Simrad EM300 transducer is hullmounted within a transducer pod that is
located midship. The system’s normal
operating frequency is approximately 30
kHz. The transmit fan-beam is split into
either three or nine narrower beam
sectors with independent active steering
to correct for vessel yaw. Angular
coverage is 36 degrees (in Extra Deep
Mode, for use in water depths 3,000 to
6,000 m) or 150 degrees (in shallower
water). The total angular coverage of 36
or 150 degrees consists of the 3 or 9
beams transmitted at slightly different
frequencies. The sectors are frequency
coded between 30 and 34 kHz and they
are transmitted sequentially at each
ping. Except in very deep water where
the total beam is 36 x 1, the composite
fan beam will overlap slightly if the
vessel yaw is less than the fore-aft width
of the beam (1,2, or 4, respectively).
Achievable swath width on a flat bottom
will normally be approximately 5x the
water depth. The maximum source level
is 237 dB re 1 µPa•m (rms)
(Hammerstand, 2005). In deep water
(500–3,000 m) a pulse length of 5 ms is
normally used. At intermediate depths
(100–1,000 m), a pulse length of 2 ms
is used, and in shallow water (<300 m),
a pulse length of 0.7 ms is used. The
ping rate is mainly limited by the round
trip travel time in the water up to a ping
rate of 10 pings/s in shallow water.
The Thompson will also utilize the
Knudsen Engineering Model 320BR subbottom profiler, which is a dualfrequency echosounder designed to
operate at 3.5 and/or 12 kHz. It is used
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 12 kHz transducer (EDO
323B) or a 3.5 kHz array of 16 ORE 137D
transducers in a 4 x 4 arrangement. The
maximum power output of the 320BR is
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10 kilowatts for the 3.5 kHz section and
2 kilowatts for the 12 kHz section.
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 the
interval is estimated to be every 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.
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 one
45–in3 GI gun, in relation to distance
and direction from the airgun(s). 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 gun 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 8,
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23, and 220 m (26.2, 75.5, and 721.8 ft),
respectively and 12, 35, and 330 m
(39.4, 115, and 1,082.7 ft), respectively
for intermediate water depths (100–
1000m, 328–3,280 ft). Because the
model results are for a 2.5–m (8.2–ft)
tow depth, the above distances slightly
underestimate the distances for the 45–
in3 GI gun towed at 4–m (13–ft) depth.
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 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 100–1,000
m (328–3,280 ft) and <100 m (328 ft).
The proposed survey will occur in
depths 650–1,200 m (2,132–3,936 ft), so
the correction factors for the latter are
not relevant here.
The empirical data indicate that, for
deep water (>1,000 m, 3,280 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 180–
and 190–dB radii are 69 m and 20 m
(226.3 and 65.6 ft), respectively.
Empirical measurements were not
conducted for intermediate depths
(100–1,000 m, 328–3,280 ft). On the
expectation that results will be
intermediate between those from
shallow and deep water, a 1.5x
correction factor is applied to the
estimates provided by the model for
deep water situations. This is the same
factor that was applied to the model
estimates during L-DEO cruises in 2003.
The assumed 180- and 190–dB radii in
intermediate-depth water are 104 m and
30 m (341.1 and 98.4 ft), respectively.
The GI guns will be shut down
immediately when cetaceans or
pinnipeds are detected within or about
to enter the measured 180–dB (rms) or
190–dB (rms) radius, respectively.
Description of Marine Mammals in the
Activity Area
Thirty-two marine mammal species,
including 19 odontocete (dolphins and
small and large toothed whales) species,
seven mysticete (baleen whales) species,
five pinniped species, and the sea otter,
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may occur or have been documented to
occur in the marine waters off Oregon
and Washington, excluding extralimital
sightings or strandings (Table 1 here).
Six of the species that may occur in the
project area are listed under the U.S.
Endangered Species Act (ESA) as
endangered, including sperm,
humpback, blue, fin, sei, and North
Pacific right whales. In addition, the
southern resident killer whale stock is
also listed as endangered, but is
unlikely to be seen in offshore waters of
Oregon. The threatened Steller sea lion
could also occur in the project area.
However, the threatened northern sea
otter is only known to occur in coastal
waters and is not expected in the project
area (the sea otter is under the
jurisdiction of the U.S. Fish and
Wildlife Service.
Gray whales are also not expected in
the project area because their
occurrence off Oregon is limited to very
shallow, coastal waters. The California
sea lion, Steller sea lion, and harbor seal
are also mainly coastal and are not
expected at the survey locations.
Information on habitat and abundance
of the species that may occur in the
study area are given in Table 1 below.
Vagrant ringed seals, hooded seals, and
ribbon seals have been sighted or
stranded on the coast of California (see
Mead, 1981; Reeves et al., 2002) and
presumably passed through Oregon
waters. A vagrant beluga was seen off
the coast of Washington (Reeves et al.,
2002).
The six species of marine mammals
expected to be most common in the
deep pelagic or slope waters of the
project area, where most of the survey
sites are located, include the Pacific
white-sided dolphin, northern right
whale dolphin, Risso’s dolphin, shortbeaked common dolphin, Dall’s
porpoise, and northern fur seal (Green et
al., 1992, 1993; Buchanan et al., 2001;
Barlow, 2003; Carretta et al., 2006).
The sperm, pygmy sperm,
mesoplodont species, Baird’s beaked,
and Cuvier’s beaked whales and the
northern elephant seal are considered
pelagic species, but are generally
uncommon in the waters near the
survey area. Additional information
regarding the distribution of these
species expected to be found in the
project area and how the estimated
densities were calculated may be found
in UTIG’s application.
Habitat
Abundance1
Rqstd Take
Inshore, occasionally offshore
N.A.2
0
Mainly nearshore waters and banks
1391
1
Pelagic and coastal
1015
1
Sei whale (Balaenoptera borealis) *
Primarily offshore, pelagic
56
0
Fin whale (Balaenoptera physalus) *
Continental slope, mostly pelagic
3279
1
Pelagic and coastal
1744
0
Usually pelagic and deep seas
1233
2
Pygmy sperm whale (Kogia breviceps)
Deep waters off the shelf
247
2
Dwarf sperm whale (Kogia sima)
Deep waters off the shelf
N.A.
0
Cuvier′s beaked whale (Ziphius cavirostris)
Pelagic
1884
0
Baird′s beaked whale (Berardius bairdii)
Pelagic
228
1
Species
Mysticetes
North Pacific right whale (Eubalaena japonica) *
Humpback whale (Megaptera novaeangliae) *
Minke whale (Balaenoptera acutorostrata)
Blue whale (Balaenoptera musculus) *
Odontocetes
Sperm whale (Physeter macrocephalus) *
Blainville′s beaked whale (Mesoplodon densirostris)
Slope, offshore
1247
3
0
Hubb′s beaked whale (Mesoplodon carlhubbsi)
Slope, offshore
1247
3
0
Stejneger′s beaked whale (Mesoplodon stejnegeri)
Slope, offshore
1247
3
0
Mesoplodon sp. (Unidentified)
Slope, offshore
1247
1
Offshore bottlenose dolphin (Tursiops truncatus)
Offshore, slope
5,065
0
Off continental shelf
13,934
0
Shelf and pelagic, seamounts
449,846
7
Offshore, slope
59,274
6
Northern right whale dolphin (Lissodelphis borealis)
Slope, offshore waters
20,362
5
Risso′s dolphin (Grampus griseus)
Shelf, slope, seamounts
16,066
3
Pelagic, occasionally inshore
N.A.
0
Widely distributed
466 (Offshore)
1
Striped dolphin (Stenella coeruleoalba)
Short-beaked common dolphin (Delphinus delphis)
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Pacific white-sided dolphin (Lagenorhynchus
obliquidens)
False killer whale (Pseudorca crassidens)
Killer whale (Orcinus orca)
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Habitat
Abundance1
Rqstd Take
Short-finned pilot whale (Globicephala
macrorhynchus)
Mostly pelagic, high-relief topography
304
0
Harbor porpoise (Phocoena phocoena)
Coastal and inland waters
39,586 (OR/WA)
0
Shelf, slope, offshore
99,517
47
Species
Dall′s porpoise (Phocoenoides dalli)
Pinnipeds
Northern fur seal (Callorhinus ursinus)
Pelagic, offshore
California sea lion (Zalophus californianus
californianus)
688,028
2
19
Coastal, shelf
NA
Coastal, pelagic when migrating
Northern elephant seal (Mirounga angustirostris)
237,000-244,000
101,000 (CA)
2
Table 1. Species expected to be encountered (and potentially harassed) during UTIG′s NE Pacific Ocean cruise.
N.A. B Data not available or species status was not assessed.
* Species are listed as threatened or endangered under the Endangered Species Act.
1 Abundance given for U.S., Eastern North Pacific, or California/Oregon/Washington Stock, whichever is included in the 2005 U.S. Pacific Marine Mammal Stock Assessments (Carretta et al. 2006), unless otherwise stated.
2 Angliss and Outlaw (2005).
3 All mesoplodont whales
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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 or non-auditory physical or
physiological effects (Richardson et al.,
1995; Gordon et al., 2004). Given the
small size of the GI guns planned for the
proposed 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 or any
significant non-auditory physical or
physiological effects. 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 UTIG’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 two GI guns planned for use in
the proposed project.
Numerous other 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 UTIG’s
application). That is often true even in
cases when the pulsed sounds appear to
be readily audible to the animals based
on measured received levels and the
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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, low-energy airgun
source planned for use in this project,
NMFS expects mammals to tolerate
being closer to this source than for a
larger airgun source typical of most
seismic surveys. Mysticetes,
odontocetes, pinnipeds and sea otters
have all been seen commonly by
observers aboard vessels conducting
small-source seismic surveys, indicating
some degree of tolerance of sounds from
small airgun sources (e.g., Calambokidis
et al., 2002; Haley and Koski, 2004;
Holst et al., 2005a; Ireland et al., 2005;
MacLean and Koski, 2005; see also ‘‘site
survey’’ portions of Stone, 2003 and
Stone and Tasker, 2006).
Masking
Obscuring of sounds of interest by
interfering sounds, generally at similar
frequencies, is known as 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
matter. 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; Smultea et al., 2004).
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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). Similar reactions
have also been shown during recent
work in the Gulf of Mexico (Tyack et al.,
2003; Smultea et al., 2004). 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 airgun to be used
here. Dolphins and porpoises are
commonly heard calling while airguns
are operating (Gordon et al., 2004;
Smultea et al., 2004; Holst et al.,
2005a,b). 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
UTIG’s application.
Disturbance Reactions
Disturbance includes a variety of
effects, including subtle changes in
behavior, more conspicuous changes in
activities, and displacement. Reactions
to sound, if any, depend on species,
state of maturity, experience, current
activity, reproductive state, time of day,
and many other factors (Richardson et
al., 1995; Wartzok et al., 2004; Southall
et al., 2007). If a marine mammal
responds to an underwater sound by
changing its behavior or moving a small
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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 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 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 UTIG’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
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
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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
UTIG’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 0.22 or
0.33 km (0.14 or 0.21 mi), as compared
with several kilometers when a large
array of airguns is operating.
Responses of humpback whales to
seismic surveys have been studied
during migration and on the summer
feeding grounds, and there has also been
discussion of effects on the Brazilian
wintering grounds. McCauley et al.
(1998, 2000) studied the responses of
humpback whales off Western Australia
to a full-scale seismic survey with a 16–
airgun, 2,678–in3 array, and to a single
20–in3 airgun with a source level of 227
dB re 1 µPa m. McCauley et al. (1998)
documented that avoidance reactions
began at 5–8 km (3.1–5 mi) from the
array, and that those reactions kept most
pods approximately 3–4 km (1.9–2.5 mi)
from the operating seismic boat.
McCauley et al. (2000) noted localized
displacement during migration of 4–5
km (2.5–3.1 mi) by traveling pods and
7–12 km (4.3–7.5 mi) by cow-calf pairs.
Avoidance distances with respect to the
single airgun were smaller but
consistent with the results from the full
array in terms of received sound levels.
Mean avoidance distance from the
airgun corresponded to a received
sound level of 140 dB re 1 µPa (rms);
that was the level at which humpbacks
started to show avoidance reactions to
an approaching airgun. The standoff
range, i.e., the closest point of approach
of the whales to the airgun,
corresponded to a received level of 143
dB re 1 µPa (rms). The initial avoidance
response generally occurred at distances
of 5–8 km (3.1–5 mi) from the airgun
array and 2 km (1.2 mi) from the single
airgun. However, some individual
humpback whales, especially males,
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approached within distances of 100–400
m (328–1,312 ft), where the maximum
received level was 179 dB re 1 µPa
(rms).
Humpback whales on their summer
feeding grounds in southeast Alaska did
not exhibit persistent avoidance when
exposed to seismic pulses from a 1.64–
L (100 in3) airgun (Malme et al., 1985).
Some humpbacks seemed ‘‘startled’’ at
received levels of 150–169 dB re 1 µPa
on an approximate rms basis. Malme et
al. (1985) conclude 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).
It has been suggested that South
Atlantic humpback whales wintering off
Brazil may be displaced or even strand
upon exposure to seismic surveys (Engel
et al., 2004). The evidence for this was
circumstantial, subject to alternative
explanations (IAGC 2004), and not
consistent with results from direct
studies of humpbacks exposed to
seismic surveys in other areas and
seasons. After allowance for data from
subsequent years, there was ‘‘no
observable direct correlation’’ between
strandings and seismic surveys (IWC
2007:236).
Results from bowhead whales show
that responsiveness of baleen whales to
seismic surveys can be quite variable
depending on the activity (migrating vs.
feeding) of the whales. Bowhead whales
migrating west across the Alaskan
Beaufort Sea in autumn, in particular,
are unusually responsive, with
substantial avoidance occurring out to
distances of 20 30 km (12.4–18.6 mi)
from a medium-sized airgun source,
where received sound levels were on
the order of 130 dB re 1 µPa (rms)
(Miller et al., 1999; Richardson et al.,
1999). However, more recent research
on bowhead whales (Miller et al.,
2005a) corroborates earlier evidence
that, during the summer feeding season,
bowheads are not as sensitive to seismic
sources. In summer, bowheads typically
begin to show avoidance reactions at a
received level of about 160–170 dB re 1
µPa (rms) (Richardson et al., 1986;
Ljungblad et al., 1988; Miller et al.,
1999). There are no data on the
reactions of wintering bowhead whales
to seismic surveys. See Appendix A (e)
of UTIG’s application for more
information regarding bowhead whale
reactions to airguns.
Reactions of migrating and feeding
(but not wintering) gray whales to
seismic surveys have been studied.
Malme et al. (1986, 1988) studied the
responses of feeding Eastern Pacific gray
whales to pulses from a single 100 in3
airgun off St. Lawrence Island in the
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northern Bering Sea. Malme et al. (1986,
1988) 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 and
on observations of Western Pacific gray
whales feeding off Sakhalin Island,
Russia (Johnson et al., 2007).
Various species of Balaenoptera (blue,
fin, sei, and minke whales) have
occasionally been reported in areas
ensonified by airgun pulses. Sightings
by observers on seismic vessels off the
U.K. from 1997 to 2000 suggest that, at
times of good sightability, numbers of
rorquals seen are similar when airguns
are shooting and not shooting (Stone,
2003). Although individual species did
not show any significant displacement
in relation to seismic activity, all baleen
whales combined were found to remain
significantly further from the airguns
during shooting compared with periods
without shooting (Stone, 2003; Stone
and Tasker, 2006). In a study off Nova
Scotia, Moulton and Miller (2005) found
little or no difference in sighting rates
and initial sighting distances of
balaenopterid whales when airguns
were operating vs. silent. However,
there were indications that these whales
were more likely to be moving away
when seen during airgun operations.
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
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for toothed whales. However, a
systematic study on sperm whales has
been done (Jochens and Biggs, 2003;
Tyack et al., 2003; Miller et al., 2006),
and there is an increasing amount of
information about responses of various
odontocetes to seismic surveys based on
monitoring studies (Stone, 2003;
Smultea et al., 2004; Bain and Williams,
2006; Holst et al., 2006; Stone and
Tasker, 2006; Moulton and Miller,
2005).
Seismic operators and marine
mammal observers 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 (Goold, 1996; Calambokidis
and Osmek, 1998; Stone, 2003). In most
cases, the avoidance radii for delphinids
appear to be small, on the order of 1 km
(0.62 mi) or less.
The beluga may be a species that (at
least at times) shows long-distance
avoidance of seismic vessels. Aerial
surveys during seismic operations in the
southeastern Beaufort Sea recorded
much lower sighting rates of beluga
whales within 10–20 km (6.2–12.4 mi)
of an active seismic vessel. These results
were consistent with the low number of
beluga sightings reported by observers
aboard the seismic vessel, suggesting
that some belugas might be avoiding the
seismic operations at distances of 10–20
km (6.2–12.4 mi) (Miller et al., 2005a).
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, 2005;
Finneran and Schlundt, 2004).
However, the animals tolerated high
received levels of sound (pk-pk level
>200 dB re 1 µPa) before exhibiting
aversive behaviors.
Results for porpoises depend on
species. Dall’s porpoises seem relatively
tolerant of airgun operations (MacLean
and Koski, 2005; Bain and Williams,
2006), whereas the limited available
data suggest that harbor porpoises show
stronger avoidance (Stone, 2003; Bain
and Williams, 2006; Stone and Tasker,
2006). This apparent difference in
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responsiveness of these two porpoise
species is consistent with their relative
responsiveness to boat traffic in general
(Richardson et al., 1995; Southall et al.,
2007).
Most studies of sperm whales exposed
to airgun sounds indicate that this
species shows considerable tolerance of
airgun pulses. In most cases, the whales
do not show strong avoidance, and they
continue to call (see Appendix A of
UTIG’s application for review).
However, controlled exposure
experiments in the Gulf of Mexico
indicate that foraging effort is
apparently somewhat reduced upon
exposure to airgun pulses from a
seismic vessel operating in the area, and
there may be a delay in diving to
foraging depth.
There are no specific data on the
behavioral reactions of beaked whales to
seismic surveys. Most beaked whales
tend to avoid approaching vessels of
other types (Wursig et al., 1998). They
may also dive for an extended period
when approached by a vessel (Kasuya,
1986). It is likely that these beaked
whales would normally show strong
avoidance of an approaching seismic
vessel, but this has not been
documented explicitly.Odontocete
reactions to large arrays of airguns are
variable and, at least for delphinids and
some porpoises, seem to be confined to
a smaller radius than has been observed
for mysticetes (see Appendix A of
UTIG’s application for more
information). Behavioral reactions of
most odontocetes to the small GI gun
source to be used here are expected to
be very localized.
Pinnipeds – Pinnipeds are not likely
to show a strong avoidance reaction to
the two GI guns 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 UTIG’s application). Ringed
seals frequently do not avoid the area
within a few hundred meters of
operating airgun arrays (Harris et al.,
2001; Moulton and Lawson, 2002;
Miller et al., 2005a). However, initial
telemetry work suggests that avoidance
and other behavioral reactions by two
other species of seals to small airgun
sources may at times be stronger than
evident to date from visual studies of
pinniped reactions to airguns
(Thompson et al., 1998). Even if
reactions of any pinnipeds that might be
encountered in the present study area
are as strong as those evident in the
telemetry study, reactions are expected
to be confined to relatively small
distances and durations, with no long-
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term effects on pinniped individuals or
populations.
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 UTIG’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 (NMFS, 2000).
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 UTIG’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 scientific data on TTS, the
expected offset between the TTS and
permanent threshold shift (PTS)
thresholds, differences in the acoustic
frequencies to which different marine
mammal groups are sensitive, and other
relevant factors.
Because of the small size of the airgun
source in this project (two 40–60 in3 GI
gun), alongwith 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 GI
guns (and multibeam echosounder and
sub-bottom profiler), 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
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(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, 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. 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, 2005).
Given the available data, the received
level of a single seismic pulse (with no
frequency weighting) might need to be
approximately 186 dB re 1 µPa2•s (i.e.,
186 dB SEL or approximately 221–226
dB pk-pk) in order to produce brief,
mild TTS. Exposure to several strong
seismic pulses that each have received
levels near 175–180 dB SEL 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. The distances
from the Thompson’s GI guns at which
the received energy level (per pulse)
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would be expected to be ≥175–180 dB
SEL are the distances shown in the 190
dB re 1 µPa (rms) column in Table 1 of
UTIG’s application (given that the rms
level is approximately 10–15 dB higher
than the SEL value for the same pulse).
Seismic pulses with received energy
levels ≥175–180 dB SEL (190 dB re 1
µPa (rms)) are expected to be restricted
to radii no more than 69–104 m (226.3–
341.1 ft) around the two GI guns. The
specific radius depends on the depth of
the water. For an odontocete closer to
the surface, the maximum radius with
≥175–180 dB SEL or ≥190 dB re 1 µPa
(rms) would be smaller. Such levels
would be limited to distances within
tens of meters of the small GI guns
source to be used in this project.
For baleen whales, direct or indirect
data do not exist on levels or properties
of sound thatare required to induce
TTS. The frequencies to which baleen
whales are most sensitive are lower than
those to which odontocetes are most
sensitive, and natural background noise
levels at those low frequencies tend to
be higher. As a result, auditory
thresholds of baleen whales within their
frequency band of best hearing are
believed to be higher (less sensitive)
than are those of odontocetes at their
best frequencies (Clark and Ellison,
2004). From this, it is suspected that
received levels causing TTS onset may
also be higher in baleen whales. In any
event, no cases of TTS are expected
given three considerations: (1) the low
abundance of baleen whales expected in
the planned study areas; (2) the strong
likelihood that baleen whales would
avoid the approaching airguns (or
vessel) before being exposed to levels
high enough for there to be any
possibility of TTS; and (3) the
mitigation measures that are proposed
to be implemented.
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
suggests that some pinnipeds may incur
TTS at somewhat lower received levels
than do small odontocetes exposed for
similar durations (Kastak et al., 1999,
2005; Ketten et al., 2001; cf. Au et al.,
2000). The TTS threshold for pulsed
sounds has been indirectly estimated as
being an SEL of about 171 dB re µPa2•s
(Southall et al., 2007), which would be
equivalent to about 181–186 dB re 1 µPa
(rms). Corresponding values for
California sea lions and northern
elephant seals are likely to be higher
(Kastak et al., 2005).
To avoid injury, NMFS has
determined that cetaceans and
pinnipeds should not be exposed to
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pulsed underwater noise at received
levels exceeding, respectively, 180 and
190 dB re 1 µPa (rms). Those sound
levels were not considered to be the
levels above which TTS might occur.
Rather, they were the received levels
above which, in the view of a panel of
bioacoustics specialists convened by
NMFS before TTS measurements for
marine mammals started to become
available, one could not be certain that
there would be no injurious effects,
auditory or otherwise, to marine
mammals. As summarized above, data
that are now available imply that TTS
is unlikely to occur unless odontocetes
(and probably mysticetes as well) are
exposed to airgun pulses stronger than
180 dB re 1 µPa (rms).
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 at least several
decibels above that inducing mild TTS
if the animal were exposed to strong
sound pulses with rapid rise time (see
Appendix A (f) of UTIG’s application).
The specific difference between the PTS
and TTS thresholds has not been
measured for marine mammals exposed
to any sound type. However, based on
data from terrestrial mammals, a
precautionary assumption is that the
PTS threshold for impulse sounds (such
as airgun pulses as received close to the
source) is at least 6 dB higher than the
TTS threshold on a peak-pressure basis
and probably more than 6 dB.
On an SEL basis, Southall et al. (2007)
estimate that received levels would
need to exceed the TTS threshold by at
least 15 dB for there to be risk of PTS.
Thus, for cetaceans they estimate that
the PTS threshold might be an SEL of
about 198 dB re 1 µPa2.s. Additional
assumptions had to be made to derive
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a corresponding estimate for pinnipeds.
Southall et al. (2007) estimate that the
PTS threshold could be an SEL of about
186 dB re 1 µPa2•s in the harbor seal;
for the California sea lion and northern
elephant seal the PTS threshold would
probably be higher. Southall et al.
(2007) also not that, regardless of the
SEL, there is concern about the
possibility of PTS if a cetacean or
pinniped received one or more pulses
with peak pressure exceeding 230 or
218 dB 1 µPa (peak).
In the proposed project employing
two 40 to 60–in3 GI guns, marine
mammals are highly 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 tens of meters of the GI guns 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 GI guns 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 the GI guns for a
period longer than the inter-pulse
interval. Baleen whales generally avoid
the immediate area around operating
seismic vessels, as do some other
marine mammals and sea turtles. The
planned monitoring and mitigation
measures, including visual monitoring
and shut downs of the GI guns when
mammals are seen within or about to
enter the ‘‘safety radii’’ or exclusion
zone (EZ), will minimize the alreadyminimal 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. However,
studies examining such effects are
limited. 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, when the sound is
strongly channeled with less-thannormal propagation loss, or when
dispersal of the animals is constrained
by shorelines, shallows, etc. Airgun
pulses, because of their brevity and
intermittence, are less likely to trigger
resonance or bubble formation than are
more prolonged sounds. It is doubtful
that any single marine mammal would
be exposed to strong seismic sounds for
time periods long enough to induce
physiological stress.
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Until recently, it was assumed that
diving marine mammals are not subject
to the bends or air embolism. This
possibility was first explored at a
workshop (Gentry [ed.], 2002) 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 bubble formation in tissues caused by
exposure to noise from naval sonar.
However, this link could not be
confirmed. Jepson et al. (2003) first
suggested a possible link between midfrequency sonar activity and acute
chronic tissue damage that results from
the formation in vivo of gas bubbles,
based on the beaked whale stranding in
the Canary Islands in 2002 during naval
exercises. Fernandez et al. (2005a)
showed those beaked whales did indeed
have gas bubble-associated lesions, as
well as fat embolisms. Fernandez et al.
(2005b) also found evidence of fat
embolism in three beaked whales that
stranded 100 km (62 mi) north of the
Canaries in 2004 during naval exercises.
Examinations of several other stranded
species have also revealed evidence of
gas and fat embolisms (Arbelo et al.,
2005; Jepson et al., 2005a; Mendez et al.,
2005). Most of the afflicted species were
deep divers. There is speculation that
gas and fat embolisms may occur if
cetaceans ascend unusually quickly
when exposed to aversive sounds, or if
sound in the environment causes the
destablization of existing bubble nuclei
(Potter, 2004; Arbelo et al., 2005;
Fernandez et al., 2005a; Jepson et al.,
2005b; Cox et al., 2006). Even if gas and
fat embolisms can occur during
exposure to mid-frequency sonar, there
is no evidence that that type of effect
occurs in response to airgun sounds.
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 shut downs of the GI guns,
will reduce any such effects that might
otherwise occur.
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Strandings and Mortality
Marine mammals close to underwater
detonations of high explosives can be
killed or severely injured, and their
auditory organs are especially
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 mass
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 of UTIG’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 (Balcomb and
Claridge, 2001; NOAA and USN, 2001;
Jepson et al., 2003; Fernandez et al.,
2004, 2005a; Cox et al., 2006), even if
only indirectly, suggests that caution is
warranted when dealing with exposure
of marine mammals to any highintensity pulsed sound.
There is no conclusive evidence of
cetacean strandings as a result of
exposure to seismic surveys.
Speculation concerning a possible link
between seismic surveys and strandings
of humpback whales in Brazil (Engel et
al., 2004) was not well founded based
on available data (IAGC, 2004; IWC,
2006). In September 2002, there was a
stranding of two Cuvier’s beaked whales
in the Gulf of California, Mexico, when
the L-DEO research vessel Maurice
Ewing was operating a 20–gun, 8,490–
in3 array in the general area. The link
between the stranding and the seismic
survey was inconclusive and not based
on any physical evidence (Hogarth,
2002; Yoder, 2002). Nonetheless, the
preceding example 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. No
injuries of beaked whales are
anticipated during the proposed study
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because of the proposed monitoring and
mitigation measures.
The proposed 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
Multibeam Echosounder Signals
A Simrad EM300 30–kHz MBES will
be operated from the source vessel
during approximately two days of the
proposed study. Sounds from the MBES
are very short pulses occurring for 2–5
ms, at a ping rate of up to 10 pings/s
depending on depth. Given the
minimum water depth in the study area
(650 m; 2–way travel time ≥0.9 s), the
pulse repetition rate is not likely to
exceed 1 ping/s. Most of the energy in
the sound pulses emitted by the MBES
is at freqencies near 30 kHz within the
audible range for odontocetes and at
least some pinnipeds, but probably not
for baleen whales (Southall et al., 2007).
The beam is narrow (1–4°) in fore-aft
extent and wide (150°) in the cross-track
extent. Each ping consists of nine beams
transmitted at slightly different
frequencies. Any given mammal at
depth near the trackline would be in the
main beam for only one or two of the
nine segments. Also, marine mammals
that encounter the Simrad EM300 are
unlikely to be subjected to repeated
pulses because of the narrow fore-aft
width of the beam and will receive only
limited amounts of pulse energy
because of the short pulses. Animals
close to the ship (where the beam is
narrowest) are especially unlikely to be
ensonified for more than one 5 ms pulse
(or two pulses if in the overlap area).
Similarly, Kremser et al. (2005) noted
that the probability of a cetacean
swimming through the area of exposure
when MBES emits a pulse is small due
to the narrow beam being emitted. The
animal would have to pass the
transducer at close range and be
swimming at speeds similar to the
vessel in order to be subjected to sound
levels that could cause TTS. Burkhardt
et al. (2007) concluded that immediate
direct injury was possible only if a
cetacean dived under the vessel into the
immediate vicinity of the transducer.
Navy sonars that have been linked to
avoidance reactions and stranding of
cetaceans (1) generally have a longer
pulse duration than the Simrad EM300,
and (2) are often directed close to
horizontally vs. more downward for the
MBES. The area of possible influence of
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the MBES is much smaller a narrow
band below the source vessel. The
duration of exposure for a given marine
mammal can be much longer for a navy
sonar. Possible effects of an MBES on
marine mammals are outlined below.
Marine mammal communications will
not be masked appreciably by the MBES
signals given its low duty cycle and the
brief period when an individual
mammal is likely to be within its beam.
Furthermore, in the case of baleen
whales, the signals (30 kHz) do not
overlap with the frequencies in the calls
or with the functional hearing range,
which would avoid any possibility of
masking.
Behavioral reactions of free ranging
marine mammals to echosounders and
other sound sources appear to vary by
species and circumstance. Observed
reactions have included silencing and
dispersal by sperm whales (Watkins et
al., 1985), increased vocalizations and
no dispersal by pilot whales (Rendell
and Gordon, 1999), and the previouslymentioned beachings by beaked whales.
During exposure to a 21–25 kHz whalefinding sonar with a source level of 215
dB re 1 µPam, gray whales showed
slight avoidance (∼200 m or 656 ft)
behavior (Frankel, 2005). 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 MBES, and a
given mammal would have received
many pulses from the naval sonars.
During UTIG’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. In the case of
baleen whales, the MBES will operate at
too high a frequency to have any effect.
Captive bottlenose dolphins and a
beluga whale exhibited changes in
behavior when exposed to 1 s pulsed
sounds at frequencies similar to those
that will be emitted by the MBES used
by UTIG, and to shorter broadband
pulsed signals. Behavioral changes
typically involved what appeared to be
deliberate attempts to avoid the sound
exposure (Schlundt et al., 2000;
Finneran et al., 2002; Finneran and
Schlundt, 2004). The relevance of those
data to free-ranging odontocetes is
uncertain, and in any case the test
sounds were quite different in either
duration or bandwidth as compared
with those from an MBES.
During a previous low-energy seismic
survey from the Thompson, the EM300
MBES was in operation most of the
time. Many cetaceans and small
numbers of fur seals were seen by
marine mammal visual observers
(MMVOs) aboard the ship, but no
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specific information about MBES effects
(if any) on mammals was obtained
(Ireland et al., 2005). These responses (if
any) could not be distinguished from
responses to the airgun (when
operating) and to the ship itself.
Given recent stranding events that
have been associated with the
operations of naval sonar, there is
concern that mid-frequency sonar
sounds can cause serious impacts to
marine mammals (see above). However,
the MBES proposed for use by UTIG is
quite different than sonars used for navy
operations. Pulse duration of the MBES
is very short relative to naval sonars.
Also, at any given location, an
individual marine mammals would be
in the beam of the MBES for much less
time given the generally downward
orientation of the beam and its narrow
fore-aft beamwidth; navy sonars often
use near horizontally directed sound.
Those factors would all reduce the
sound energy received from the MBES
rather drastically relative to that from
the sonars used by the navy.
Although the source level of the
Simrad EM300 is not available, the
maximum source level of a relatively
powerful MBES (Simrad EM120) is 242
dB re 1 µParms. At that source level, the
received level for an animals within the
MBES beam 100 m below the ship
would be ∼202 dB re 1 µPa (rms),
assuming 40 dB of spreading loss over
100 m (circular spreading). Given the
narrow beam, only one pulse is likely to
be received by a given animal. The
received energy from a single pulse of
duration 5 ms would be about 179 dB
1 µPa•s, i.e., 202 dB+10 log (0.005 s).
That would be below the TTS
thresholds for an odontocete or
pinniped exposed to a single nonimpulsive sonar transmission (195 and
≥183 dB re 1 µPa•s, respectively) and
even further below the anticipated PTS
threshold (215 and ≥203 dB re 1 µPa•s,
respectively) (Southall et al., 2007). In
contrast, an animal that was only 10 m
below the MBES when a ping is emitted
would be expected to receive a level 20
dB higher, i.e., 199 dB re 1 Pa s in the
case of the EM120. That animal might
incur some TTS (which would be fully
recoverable), but the exposure would
still be below the anticipated PTS
threshold for both cetaceans and
pinnipeds.
Chirp Echosounder Signals
A chirp echosounder or sub-bottom
profiler will be operated from the source
vessel at all times during the proposed
study. Sounds from the sub-bottom
profiler are very short pulses, occurring
for up to 24 ms once every few seconds.
Most of the energy in the sound pulses
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emitted by this sub-bottom profiler is at
12 kHz, and the beam is directed
downward. The source level of the chirp
is expected to be lower than that of the
MBES. Kremser et al. (2005) noted that
the probability of a cetacean swimming
through the area exposure when an
echosounder emits a pulse is small, and
if the animal was in the area, it would
have to pass the transducer at close
range in order to be subjected to sound
levels that could cause TTS.
Marine mammal communications will
not be masked appreciably by the subbottom profiler signals given their
directionality and the brief period when
an individual mammal is likely to be
within its beam. Furthermore, in the
case of most odontocetes, the sonar
signals do not overlap with the
predominant frequencies in the calls,
which would avoid significant masking.
Marine mammal behavioral reactions
to other pulsed sound sources are
discussed above, and responses to the
sub-bottom profiler are likely to be
similar to those for other pulsed sources
if received at the same levels. However,
the pulsed signals from the chirp are
somewhat weaker than those from the
MBES. Therefore, behavioral responses
are not expected unless marine
mammals are very close to the source.
Source levels of the chirp are much
lower than those of the airguns and the
MBES, which are discussed above.
Thus, it is unlikely that the chirp
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 chirp is often operated
simultaneously with other higher-power
acoustic sources. Many marine
mammals will move away in response
to the approaching higher-power
sources or the vessel itself before the
mammals would be close enough for
there to be any possibility of effects
from the less intense sounds from the
chirp. In the case of mammals that do
not avoid the approaching vessel and its
various sound sources, mitigation
measures that would be applied to
minimized effects of the higher-power
sources would further reduce or
eliminate any minor effects of the chirp.
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
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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 Pacific
Ocean. The estimates are based on data
concerning marine mammal densities
(numbers per unit area) obtained during
surveys off Oregon and Washington
during 1996 and 2001 by NMFS
Southwest Fisheries Science Center
(SWFSC) and estimates of the size of the
area where effects potentially could
occur.
The following estimates are based on
a consideration of the number of marine
mammals that might be disturbed
appreciably by operations with the two
GI guns to be used during
approximately 1275 line-km of surveys
off the coast of Oregon in the
northeastern Pacific Ocean. The
anticipated radii of influence of the
echosounders are less than those for the
GI guns. It is assumed that, during
simultaneous operations of the GI guns
and echosounders, any marine
mammals close enough to be affected by
the echosounders would already be
affected by the airgun. However,
whether or not the GI guns are operating
simultaneously with the echosounders,
marine mammals are expected to exhibit
no more than short-term and
inconsequential responses to the
echosounders, given their
characteristics (e.g., narrow downwarddirected beam) and other considerations
described previously. Therefore, no
additional allowance is included for
animals that might be affected by the
echosounders.
Extensive systematic aircraft- and
ship-based surveys have been
conducted for marine mammals offshore
of Oregon and Washington (Bonnell et
al., 1992; Green et al., 1992, 1993;
Barlow, 1997, 2003; Barlow and Taylor,
2001; Calambokidis and Barlow, 2004;
Barlow and Forney, 2007). The most
comprehensive and recent density data
available for cetacean species off slope
and offshore waters of Oregon are from
the 1996 and 2001 NMFS/SWFSC
‘‘ORCAWALE’’ or ‘‘CSCAPE’’ ship
surveys as synthesized by Barlow and
Forney (2007). The surveys were
conducted up to approximately 550 km
(342 mi) offshore from June or July to
early November or December.
Systematic, offshore, at-sea survey data
for pinnipeds are more limited. The
most comprehensive studies are
reported by Bonnell et al. (1992) and
Green et al. (1993) based on systematic
aerial surveys conducted in 1989 1990
and 1992, primarily from coastal to
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slope waters with some offshore effort
as well.
Oceanographic conditions, including
occasional El Nino and La Nina events,
influence the distribution and numbers
of marine mammals present in the
northeastern Pacific Ocean, including
Oregon, resulting in considerable yearto-year variation in the distribution and
abundance of many marine mammal
species (Forney and Barlow, 1998;
Buchanan et al., 2001; Escorza-Trevino,
2002; Ferrero et al., 2002; Philbrick et
al., 2003). Thus, for some species the
densities derived from recent surveys
may not be representative of the
densities that will be encountered
during the proposed seismic survey.
Table 3 in UTIG’s application gives
the average and maximum densities for
each species or species group of marine
mammals reported off Oregon and
Washington (and used to calculate the
take estimates in Table 1 here),
corrected for effort, based on the
densities reported for the 1996, 2001,
and 2005 surveys (Barlow, 2003). The
densities from these 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
trackline [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
trackline, and it is measured by g(0).
Table 3 also includes mean density
information for three of the five
pinnipeds species that occur off Oregon
and Washington and mean and
maximum densities for one of those
species, from Bonnell et al. (1992).
Densities were not calculated for the
other two species because of the small
number of sightings on systematic
transect surveys.
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, and equipment malfunctions
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
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overestimate the actual numbers of
marine mammals that might be
involved. These estimates assume that
there will be no weather, equipment, or
mitigation delays, which is unlikely.
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
maximum estimates are based on the
average and maximum estimates of
densities reported by Barlow and
Forney (2007) and Bonnel et al. (1992)
described above. The estimated
numbers of potential individuals
exposed are based on the 160–dB re 1
µPa rms criterion for all cetaceans and
pinnipeds, and also based on the 170–
dB criterion for delphinids and
pinnipeds only. It is assumed that
marine mammals exposed to airgun
sounds this strong might change their
behavior sufficiently to be considered
‘‘take by harassment’’. UTIG 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 number of different individuals
that may be exposed to GI-gun sounds
with received levels ≥160 dB re 1 µPa
(rms) on one or more occasions can be
estimated by considering the total
marine area that would be within the
160 dB radius around the operating GI
guns on at least one occasion. The
proposed seismic lines do not run
parallel to each other in close proximity,
which minimizes the number of times
an individual mammal may be exposed
during the survey. However, it is
unlikely that a particular animal would
stay in the area during the entire survey.
The best estimates in this section are
based on the average of the densities
from the 1996, 2001, and 2005 NMFS
surveys, and maximum estimates are
based on the higher estimate. Table 4 in
UTIG’s application (and used to
calculate the take estimates in Table 1
here) shows the best and maximum
estimates of the number of marine
mammals that could potentially be
affected during the seismic survey.
The number of different individuals
potentially exposed to received levels
≥160 dB re 1 µPa (rms) was calculated
by multiplying:
• The expected species density, either
‘‘mean’’ (i.e., best estimate) or
‘‘maximum, ‘‘ times
• The anticipated minimum area to
be ensonified to that level during the GI
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guns operations including overlap
(exposures), or
• The anticipated minimum area to
be ensonified to that level during GI gun
operations excluding overlap
(individuals).
The area expected to be ensonified
was determined by entering the planned
survey lines into a MapInfo Geographic
Information System (GIS), using the GIS
to identify the relevant areas by
‘‘drawing’’ the applicable 160 dB or 170
dB buffer around each seismic line and
then calculating the total area within the
buffers. Areas where overlap occurred
(because of intersecting lines) were
included only once to determine the
minimum area expected to be
ensonified.
Applying the approach described
above, approximately 189 km2 would be
within the 160 dB isopleth on one or
more occasions during the survey,
whereas approximately 1,391 km2 is the
area ensonified when overlap is
included. Because this approach does
not allow for turnover in the mammal
populations in the study area during the
course of the survey, the actual number
of individuals exposed may be
underestimated. However, this will be
offset to some degree by the fact that the
160 dB (and other) distances assumed
here actually apply to a pair of slightly
larger GI guns to be used in the project.
In addition, the approach assumes that
no cetaceans will move away or toward
the trackline as the Thompson
approaches in response to increasing
sound levels prior to the time the levels
reach 160 dB. Another way of
interpreting the estimates that follow is
that they represent the number of
individuals that are expected (in the
absence of a seismic program) to occur
in the waters that will be exposed to
≥160 dB re 1 µPa (rms).
The ‘‘best estimate’’ of the number of
individual cetaceans that might be
exposed to seismic sounds with
received levels ≥160 dB re 1 µPa (rms)
during the surveys is 42 (Table 4 in
UTIG’s application). The total does not
include any endangered or beaked
whales. Dall’s porpoise is estimated to
be the most common species exposed;
the best estimates for those species are
28 (Table 4 in UTIG application). The
best estimate of the number of
exposures of cetaceans to seismic
sounds with received levels ≥160 dB re
1 µPa (rms) during the survey is 536,
including 1 humpback whale, 1 fin
whale, and 2 sperm whales. Dall’s
porpoise was exposed most frequently,
with a best estimate of 209 exposures.
The ‘‘maximum estimate’’ column in
Table 4 of UTIG’s application shows an
estimated total of 85 cetaceans that
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might be exposed to seismic sounds
≥160 dB during the surveys. In most
cases, those estimates are based on
survey data, as described above. For
endangered species, the ’maximum
estimate’ is the mean group size (from
Barlow and Forney, in press) in cases
where the calculated maximum number
of individuals exposed was between
0.05 and the mean group size
(humpback, fin, blue, and sperm
whales). The numbers for which take
authorization is requested, given in the
far right column of Table 4 in UTIG’s
application are the maximum estimates.
Based on the abundance numbers given
in UTIG’s application and Table 1 here
for non-listed cetacean species, NMFS
believes that the estimated take numbers
are small relative to the stock sizes for
these species (i.e., no more than 0.4
percent of any species).
The best and maximum estimates of
the numbers of exposures to ≥170 dB for
all delphinids during the surveys are 9
and 13, respectively. Corresponding
estimates for Dall’s porpoise are 17 and
29. The estimates are based on the
predicted 170 dB radii around the GI
guns to be used during the study and are
considered to be more realistic estimates
of the number of individual delphinids
and Dall’s porpoises that may be
affected.
Only two of the five pinniped species
discussed in Section III of UTIG’s
application the northern fur seal and the
northern elephant seal are likely to
occur in the offshore and slope waters;
the other three species of pinnipeds
known to occur regularly off Oregon and
Washington the California sea lion,
Steller sea lion, and harbor seal are
infrequent there. This conclusion is
based on results of extensive aerial
surveys conducted from the coast to
offshore waters of Oregon and
Washington (Bonnell et al., 1992; Green
et al., 1993; Buchanan et al., 2001;
Carretta et al., 2007). However, the
available density data are probably not
truly representative of densities that
could be encountered during surveys, as
the data were averaged over a number
of months and over coastal, shelf, slope,
and offshore waters. These factors
strongly influence the densities of these
pinnipeds at sea, as all pinnipeds off
Oregon and Washington exhibit
seasonal and/or inshore offshore
movements largely related to breeding
and feeding (Bonnell et al., 1992;
Buchanan et al., 2001; Carretta et al.,
2007).
Most pinnipeds, like delphinids, seem
to be less sensitive to airgun sounds
than are mysticetes. Thus, the numbers
of pinnipeds likely to be exposed to
received levels ≥170 dB re 1 µPa (rms)
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were also calculated, based on the
estimated 170–dB radii in Table 1 of
UTIG’s application. For operations in
deep water, the estimated 160 and 170
dB radii are very likely over-estimates of
the actual 160- and 170–dB distances
(Tolstoy et al., 2004a,b). Thus, the
resulting estimates of the numbers of
pinnipeds exposed to such levels may
be overestimated.
The methods described previously for
cetaceans were also used to calculate
exposure numbers for the one pinniped
species likely to be in the survey area
and whose densities were estimated by
Bonnell et al. (1992). Based on the
‘‘best’’ densities, two northern fur seals
are considered likely to be exposed to GI
gun sounds ≥160 dB re 1 µPa (rms). The
‘‘Maxim Estimate’’ column in Table 4 of
UTIG’s application shows an estimated
19 northern fur seals that could be
exposed to GI airgun sounds ≥160–dB or
≥170dB re 1 µPa (rms), respectively,
during the survey. Also included are
low maximum estimates for the
northern elephant seals, a species that
likely would be present but whose
density was not calculated because of
the small number of sightings on
systematic transect surveys. The
numbers of which ‘‘take authorization’’
is requested, given in the far right
column of Table 4 of UTIG’s
application, are based on the maximum
160 dB estimates.
The proposed UTIG seismic survey in
the northeastern Pacific Ocean involves
towing two GI guns that introduce
pulsed sounds into the ocean, as well as
echosounder operations. A towed PCable system will be deployed to
receive and record the returning signals.
Routine vessel operations, other than
the proposed GI gun operations, are
conventionally assumed not to affect
marine mammals sufficiently to
constitute ‘‘taking.’’ No ‘‘taking’’ of
marine mammals is expected in
association with operations of the
echosounders given the considerations
discussed in section IV(1)(b) of UTIGS’s
application, i.e., sounds are beamed
downward, the beam is narrow, and the
pulses are extremely short.
Strong avoidance reactions by several
species of mysticetes to seismic vessels
have been observed at ranges up to 6–
8 km (3.7–5 mi) and occasionally as far
as 20–30 km (12.4–18.6 mi) from the
source vessel when much larger airgun
arrays have been used. However,
reactions at the longer distances appear
to be atypical of most species and
situations and in any case apply to
larger airgun systems than will be used
in this project. If mysticetes are
encountered, the numbers estimated to
occur within the 160 dB isopleth in the
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survey area are expected to be very low.
In addition, the estimated numbers
presented in Table 4 of UTIG’s
application are considered
overestimates of actual numbers because
the estimated 160 and 170 dB radii used
here are probably overestimates of the
actual 160 and 170 dB radii at deepwater locations such as the present
study areas (Tolstoy et al., 2004a,b). In
addition, the radii were based on a
larger airgun source than the one
proposed for use during the present
survey.
Odontocete reactions to seismic
pulses, or at least the reactions of
delphinids and Dall’s porpoises are
expected to extend to lesser distances
than are those of mysticetes. Odontocete
low-frequency hearing is less sensitive
than that of mysticetes, and delphinids
and Dall’s porpoises are often seen from
seismic vessels. In fact, there are
documented instances of dolphins and
Dall’s porpoises approaching active
seismic vessels. However, delphinids
and porpoises (along with other
cetaceans) sometimes show avoidance
responses and/or other changes in
behavior when near operating seismic
vessels.
Taking into account the mitigation
measures that are proposed in UTIG’s
application, effects on cetaceans are
generally expected to be limited to
avoidance of the area around the
seismic operation and short-term
changes in behavior, falling within the
MMPA definition of ‘‘Level B
harassment.’’ Furthermore, the
estimated numbers of animals
potentially exposed to sound levels
sufficient to cause appreciable
disturbance are very low percentages of
the regional population sizes. The best
estimates of the numbers of individual
cetaceans (33 for all species combined)
that would be exposed to sounds ≥160
dB re 1 µPa (rms) during the proposed
survey represent, on a species-byspecies basis, no more than 0.11
pertcent of the regional populations (see
Table 4 of UTIG’s application). Dall’s
porpoise is the cetacean species with
the highest estimated number of
individuals exposed to ≥160 dB.
Varying estimates of the numbers of
marine mammals that might be exposed
to the GI guns sounds during the
proposed summer 2008 seismic survey
in the northeastern Pacific Ocean have
been presented, depending on the
specific exposure criterion (≥160 or
≥170 dB) and density criterion used
(best or maximum). The request ‘‘take
authorization’’ for each species is based
on the estimated maximum number of
individuals that might be exposed to
≥160 re 1 µPa (rms). That figure likely
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overestimates (in most cases by a large
margin) the actual number of animals
that will be exposed to and will react to
the seismic sounds. The reasons for that
conclusion are outlined above. The
relatively short-term exposures are
unlikely to result in any long-term
negative consequences for the
individuals or their populations.
The many cases of apparent tolerance
by cetaceans of seismic exploration,
vessel traffic, and some other human
activities show that co-existence is
possible. Mitigation measures such as
controlled speed, course alteration, look
outs, non-pursuit, and shut downs when
marine mammals are seen within
defined ranges should further reduce
short-term reactions, and minimize any
effects on hearing sensitivity. In all
cases, the effects are expected to be
short-term, with no lasting biological
consequence.
Only two of the five pinniped species
discussed in Section III of UTIG’s
application, the northern fur seal and
northern elephant seal, are likely to
occur in the offshore and slope waters
of the study area. A best estimate of a
single northern fur seal could be
exposed to airgun sounds with received
levels ≥160 dB re 1 µPa (rms). The
numbers for which ‘‘take authorization’’
is requested are given in the far right
column of Table 4 of UTIG’s
application. As for cetaceans, the
estimated numbers of pinnipeds that
may be exposed to received levels ≥160
dB are probably overestimates of the
actual numbers that will be affected,
and are very small proportions of the
respective population sizes.
Potential Effects on Habitat
The proposed seismic surveys 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 activity 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,
unlike explosives, they have not been
associated with any appreciable fish
kills. However, the existing body of
information relating to the impacts of
seismic surveys on marine fish (see
Appendix B of UTIG’s application) 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
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temporary or permanent sub-lethal
damage to the animals, physiological
effects include temporary and
permanent primary and secondary stress
responses, such as changes in levels of
enzymes and proteins. Behavioral
effects refer to temporary and 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 specific received levels at which
permanent adverse effects to fish
potentially could occur are little studies
and largely unknown. Furthermore,
available information on the impacts of
seismic surveys on marine fish and
invertebrates is from studies of
individuals or portions of a population;
there have been no studies at the
population scale. Thus, available
information provides limited insight on
possible real world effects at the ocean
or population scale. This makes drawing
conclusions about impacts on fish
problematic because ultimately, the
most important aspect of potential
impacts relates to how exposure to
seismic survey sound affects marine fish
populations and their viability,
including their availability to fisheries.
The following sections provide an
general overview of the available
information that exists on the effects of
exposure to seismic surveys and other
anthropogenic sound as relevant to fish
and invertebrates. The information
comprises results from scientific studies
of varying degrees of soundness and
some anecdotal information.
Pathological Effects – The potential
for pathological damage to hearing
structures in fish depends on the energy
level of the received sound and the
physiology and hearing capability of the
species in question (see Appendix B of
UTIG’s application). For a given sound
to result in hearing loss, the sound must
exceed, by some specific amount, the
hearing threshold of the fish for that
sound (Popper, 2005). The
consequences of temporary or
permanent hearing loss in individual
fish on a fish population is unknown;
however, it likely depends on the
number of individuals affected and
whether critical behaviors involving
sound (e.g., predator avoidance, prey
capture, orientation and navigation,
reproduction, etc.) are adversely
affected.
Little is known about the mechanisms
and characteristics of damage to fish
that may be inflicted by exposure to
seismic survey sounds. Few data have
been presented in the peer-reviewed
scientific literature. There are two valid
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papers with proper experimental
methods, controls, and careful
pathological investigation implicating
sounds produced by actual seismic
survey airguns with adverse anatomical
effects. One such study indicated
anatomical damage and the second
indicated TTS in fish hearing. McCauley
et al. (2003) found that exposure to
airgun sound caused observable
anatomical damage to the auditory
maculae of ‘‘pink snapper’’ (Pagrus
auratus). This damage in the ears had
not been repaired in fish sacrificed and
examined almost two months after
exposure. On the other hand, Popper et
al. (2005) documented only TTS (as
determined by auditory brainstem
response) in two of three fishes from the
Mackenzie River Delta. This study
found that broad whitefish (Coreogonus
nasus) that received a sound exposure
level of 177 dB re 1 µPa2•s showed no
hearing loss. During both studies, the
repetitive exposure to sound was greater
than would have occurred during a
typical seismic survey. However, the
substantial low-frequency energy
produced by the airgun arrays [less than
approximately 400 Hz in the study by
McCauley et al. (2003) and less than
approximately 200 Hz in Popper et al.
(2005)] likely did not propagate to the
fish because the water in the study areas
was very shallow (approximately 9 m,
29.5 ft, in the former case and <2 m, 6.6
ft, in the latter). Water depth sets a
lower limit on the lowest sound
frequency that will propagate (the
‘‘cutoff frequency’’) at about one-quarter
wavelength (Urick, 1983; Rogers and
Cox, 1988).
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; 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 40–60–in3 GI guns).
Numerous other studies provide
examples of no fish mortality upon
exposure to seismic sources (Falk and
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Lawrence, 1973; Holliday et al., 1987;
La Bella et al., 1996; Santulli et al.,
1999; McCauley et al., 2000a, 2000b,
2003; Bjarti, 2002; Hassel et al., 2003;
Popper et al., 2005).
Except for these two studies, at least
with airgun-generated sound treatments,
most contributions rely on rather
subjective assays such as fish ‘‘alarm’’ or
‘‘startle response’’ or changes in catch
rates by fishers. These observations are
important in that they attempt to use the
levels of exposures that are likely to be
encountered by most free-ranging fish in
actual survey areas. However, the
associated sound stimuli are often
poorly described, and the biological
assays are varied (Hastings and Popper,
2005).
Some studies have reported that
mortality of fish, fish eggs, or larvae can
occur close to seismic sources
(Kostyuchenko, 1973; Dalen and
Knutsen, 1986; Booman et al., 1996;
Dalen et al., 1996). Some of the reports
claimed seismic effects from treatments
quite different from actual seismic
survey sounds or even reasonable
surrogates. 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.Some studies
have reported, some equivocally, that
mortality of fish, fish eggs, or larvae can
occur close to seismic sources
(Kostyuchenko, 1973; Dalen and
Knutsen, 1986; Booman et al., 1996;
Dalen et al., 1996). Some of the reports
claimed seismic effects from treatments
quite different from actual seismic
survey sounds or even reasonable
surrogates suggested that seismic survey
sound has a limited pathological impact
on early developmental stages of
crustaceans (Pearson et al., 1994;
Christian et al., 2003; DFO, 2004).
However, the impacts appear to be
either temporary or insignificant
compared to what occurs under natural
conditions. Controlled field experiments
on adult crustaceans (Christian et al.,
2003, 2004; DFO, 2004) and adult
cephalopods (McCauley et al., 2000a,b)
exposed to seismic survey sound have
not resulted in any significant
pathological impacts on the animals. It
has been suggested that exposure to
commercial seismic survey activities
has injured giant squid (Guerra et al.,
2004), but there is no evidence to
support such claims.
Physiological Effects – Physiological
effects refer to cellular and/or
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biochemical responses of fish to
acoustic stress. Such stress potentially
could affect fish populations by
increasing mortality or reducing
reproductive success. Primary and
secondary stress responses of fish after
exposure to seismic survey sound
appear to be temporary in all studies
done to date (Sverdrup et al., 1994;
McCauley et al., 2000a, 2000b). The
periods necessary for the biochemical
changes to return to normal are variable
and depend on numerous aspects of the
biology of the species and of the sound
stimulus (see Appendix B of UTIG’s
application for more information on the
effects of airgun sounds on marine fish).
Such stress could potentially affect
animal populations by reducing
reproductive capacity and adult
abundance and increasing mortality.
Behavioral Effects – Behavioral effects
include changes in the distribution,
migration, mating, and catchability of
fish populations. Studies investigating
the possible effects of sound (including
seismic sound) on fish behavior have
been conducted on both uncaged and
caged individuals (e.g., Chapman and
Hawkings, 1969; Pearson et al., 1992;
Santulli et al., 1999, Wardle et al., 2001,
Hassel et al., 2003). Typically, in these
studies fish exhibited sharp ‘‘startle’’
response at the onset of a sound
followed by habituation and a return to
normal behavior after the sound ceased.
There is general concern about
potential adverse effects of seismic
operations on fisheries, namely a
reduction in the ‘‘catchability’’ of fish
involved in fisheries. Although reduced
catch rates have been observed in some
marine fisheries during seismic testing,
in a number of cases the findings are
confounded by other sources of
disturbance (Dalen and Raknes, 1985;
Dalen and Knutsen, 1986; L kkeborg,
1991; Skalski et al., 1992; Engas et al.,
1996). In other airgun experiments,
there was no change in CPUE of fish
when airgun pulses were emitted,
particularly in the immediate vicinity of
the seismic survey (Pickett et al., 1994;
La Bella et al., 1996). For some species,
reductions in catch may have resulted
from a change in behavior of the fish,
e.g., a change in vertical or horizontal
distribution, as reported in the Slotte et
al. (2004).
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
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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
2008 is predicted to have negligible to
low physical effects on the various life
stages of fish and invertebrates for its
relatively short duration (approximately
150 total hours at each of the three sites
off the coast of Oregon) and
approximately 975 km (606 mi) extent.
Therefore, physical effects of the
proposed program on the fish and
invertebrates would be not significant.
Behavioral Effects – Because of the
apparent lack of serious pathological
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, mating, 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 (Chapman and Hawkins, 1969;
Pearson et al., 1992; Santulli et al.,
1999; Wardle et al., 2001; Hassel et al.,
2003). Typically, in these studies fish
exhibited a sharp ‘‘startle’’ response at
the onset of a sound followed by
habituation and a return to normal
behavior after the sound ceased.
There is general concern about
potential adverse effects of seismic
operations on fisheries, namely a
potential reduction in the ‘‘catchability’’
of fish involved in fisheries. Although
reduced catch rates have been observed
in some marine fisheries during seismic
testing, in a number of cases the
findings are confounded by other
sources of disturbance (Dalen and
Raknes, 1985; Dalen and Knutsen, 1986;
L kkeborg, 1991; Skalski et al., 1992;
Engas et al., 1996). In other airgun
experiments, there was no change in
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catch per unit effort of fish when airgun
pulses were emitted, particularly in the
immediate vicinity of the seismic survey
(Pickett et al., 1994; La Bella et al.,
1996). For some species, reductions in
catch may have resulted from a change
in behavior of the fish (e.g., a change in
vertical or horizontal distribution) as
reported in Slotte et al. (2004).
In general, any adverse effects on fish
behavior or fisheries attributable to
seismic testing may depend on the
species in question and the nature of the
fishery (season, duration, fishing
method). They may also depend on the
age of the fish, its motivational state, its
size, and numerous other factors that are
difficult, if not impossible, to quantify at
this point, given such limited data on
effects of airguns on fish, particularly
under realistic at-sea conditions.
In general, any adverse effects on fish
behavior or fisheries attributable to
seismic testing may depend on the
species in question and the nature of the
fishery (season, duration, fishing
method). They may also depend on the
age of the fish, its motivational state, its
size, and numerous other factors that are
difficult, if not impossible, to quantify at
this point, given such limited data on
effects of airguns on fish, particularly
under realistic at-sea conditions.
Effects on Invertebrates
The existing body of information on
the impacts of seismic survey sound on
marine invertebrates is very limited.
However, there is some unpublished
and very limited evidence of the
potential for adverse effects on
invertebrates, thereby justifying further
discussion and analysis of this issue. Th
three types of potential effects of
exposure to seismic surveys on marine
invertebrates are pathological,
physiological, and behavioral. Based on
the physical structure of their sensory
organs, marine invertebrates appear to
be specialized to respond to particle
displacement components of an
impinging sound field and not to the
pressure component (Popper et al. 2001;
see also Appendix C of UTIG’s
application).
The only information available on the
impacts of seismic surveys on marine
invertebrates involves studies of
individuals; there have been no studies
at the population scale. Thus, available
information provides limited insight on
possible real world effects at the
regional or ocean scale. The most
important aspect of potential impacts
concerns how exposure to seismic
survey sound ultimately affects
invertebrate populations and their
viability, including availability to
fisheries.
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The following sections provide a
synopsis of available information on the
effects of exposure to seismic survey
sound on species of decapod
crustaceans and cephalopods, the two
taxonomic groups of invertebrates on
which most such studies have been
conducted. The available information is
from studies with variable degrees of
scientific soundness and from anecdotal
information.
Pathological Effects – In water, lethal
and sub-lethal injury to organisms
exposed to seismic survey sound could
depend on at least two features of the
sound source: (1) the received peak
pressure, and (2) the time required for
the pressure to rise and decay. Generally
as received pressure increases, the
period for the pressure to rise and decay
decreases, and the chance of acute
pathological effects increases. For the
two GI guns planned for the proposed
program, the pathological (mortality)
zone for crustaceans and cephalopods is
expected to be within a few metes of the
seismic source; however, very few
specific data are available on levels of
seismic signals that might damage these
animals. This premise is based on the
peak pressure and rise/decay time
characteristics of seismic airgun arrays
currently in use around the world.
Some studies have suggested that
seismic survey sound has a limited
pathological impact on early
developmental stage of crustaceans
(Pearson et al., 1994; Christian et al.,
2003; DFO, 2004). However, the impacts
appear to be either temporary or
insignificant compared to what occurs
under natural conditions. Controlled
field experiments on adult crustaceans
(Christian et al., 2003, 2004; DFO 2004)
and adult cephalopods (McCauley et al.,
2000a,b) exposed to seismic survey
sound have not resulted in any
significant pathological impacts on
animals. It has been suggested that
exposure to commercial seismic survey
activities has injured giant squid
(Guerra et al., 2003), but there is no
evidence to support such claims.
Physiological Effects – Physiological
effects refer mainly to biochemical
responses by marine invertebrates to
acoustic stress. Such stress potentially
cold affect invertebrate populations by
increasing mortality or reducing
reproductive success. Any primary and
secondary stress responses (i.e. changes
in haemolymph levels of enzymes,
proteins, etc.) of crustaceans after
exposure seismic survey sounds appear
to be temporary (hours to days) in
studies done to date (Payne et al., 2007).
The periods necessary for these
biochemical changes to return to normal
are variable and depend on numerous
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30091
aspects of the biology of the species and
of the sound stimulus.
Behavioral Effects – There is
increasing interest in assessing the
possible direct and indirect effects of
seismic and other sounds on
invertebrate behavior, particularly in
relation to the consequences for
fisheries. Changes in behavior could
potentially affect such aspects as
reproductive success, distribution,
susceptibility to predation, and
catchability by fisheries. Studies
investigating the possible behavioral
effects of exposure to seismic survey
sound on crustaceans and cephalopods
have been conducted on both uncaged
and caged animals. In some cases,
invertebrates exhibited startle responses
(e.g., squid in McCauley et al., 2000a,b).
In other cases, no behavioral impacts
were noted (e.g., crustaceans in
Christian et al., 2003, 2004; DFO, 2004).
Ther have been anecdotal reports of
reduced catch rates of shrimp shortly
after exposure to seismic survey;
however, other studies have not
observed any significant changes in
shrimp catch rate (Andriguetto-Filho et
al., 2005). Any adverse effects on
crustacean and cephalopod behavior or
fisheries attributable to seismic survey
sound depend on the species in
question and the nature of the fishery
(season, duration, fishing method).
During the proposed study, only a
small fraction of the available habitat
would be ensonified at any given time,
and fish and invertebrate 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
duration (total of approximately 150
hours) and 975 km (606 mi) extent.
Because of the reasons noted above
and the nature of the proposed activities
(small airgun 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.
Similarly, any effects to food sources are
expected to be negligible.
The effects of the proposed activity on
marine mammal habitats and food
resources are expected to be negligible,
as described above. A small minority of
the marine mammals that are present
near the proposed activity may be
temporarily displaced as much as a few
kilometers by the planned activity.
During the proposed survey, marine
mammals will be distributed according
to their habitat preferences, in shelf,
slope, and pelagic waters.
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dwashington3 on PRODPC61 with NOTICES
Concentrations of marine mammals
and/or marine mammal prey species are
not expected to occur in or near the
proposed study area, and that area does
not appear to constitute an area of
localized or critical feeding, breeding, or
migration for any marine mammal
species. The proposed activity is not
expected to have any habitat-related
effects that could cause significant or
long-term consequences for individual
marine mammals or their populations,
because operations at the various sites
will be limited in duration.
Proposed Monitoring
Vessel-based marine mammal visual
observers (MMVOs) will be aboard the
seismic source vessel and will watch for
marine mammals near the vessel during
all daytime GI gun operations and
during start-ups of the gun at night.
MMVOs will also watch for marine
mammals near the seismic vessel for at
least 30 minutes prior to the start of GI
gun operations after an extended shut
down. When feasible, MMVOs will also
make observations during daytime
periods when the seismic system is not
operating for comparison of sighting
rates and behavior with vs. without GI
guns operations. Based on MMVO
observations, the GI guns will be shut
down when marine mammals are
observed within or about to enter a
designated exclusion zone (EZ; safety
radius). The EZ is a region in which a
possibility exists of adverse effects on
animal hearing or other physical effects.
MMVOs will be appointed by the
academic institution conducting the
research cruise, with NMFS Office of
Protected Resources concurrence. A
total of three MMVOs are planned to be
aboard the source vessel. At least one
MMVO will monitor the EZ during
daytime GI guns operations and any
night-time startups. MMVOs will
normally work in daytime shifts of 4
hours duration or less. The vessel crew
will also be instructed to assist in
detecting marine mammals.
The Thompson will serve as the
platform from which MMVOs will
watch for marine mammals before and
during the GI guns operations. Two
locations are likely as observation
stations onboard the Thompson. At one
station on the bridge, the eye level will
be approximately 13.8 m (45.3 ft) above
sea level and the location will offer a
good view around the vessel
(approximately 310 degrees for one
observer and a full 360 degrees when
two observers are stationed at different
vantage points). A second observation
station is the 03 deck where the
observer’s eye level will be
approximately 10.8 m (35.4 ft) above sea
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15:34 May 22, 2008
Jkt 214001
level. The 03 deck offers a view of 330°
for two observers.
Standard equipment for MMVOs will
be 7 x 50 reticle binoculars and optical
range finders. At night, night-vision
devices (NVDs) will be available. Vessel
lights and/or NVDs are useful in
sighting some marine mammals at the
surface within a short distance from the
ship (within the EZ for the two GI guns).
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 GI guns shut
down.
MMVOs will record data to estimate
the numbers of marine mammals
exposed to various received sound
levels and to document any apparent
disturbance reactions. Data will be used
to estimate the numbers of mammals
potentially ‘‘taken’’ by harassment (as
defined in the MMPA). They will also
provide the information needed to order
a shutdown of the two GI guns when a
marine mammal is within or near the
EZ. 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 the GI
gun or 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, 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 marine mammal observations and
information regarding airgun operations
will be recorded in a standardized
format. Data accuracy will be verified by
the MMVOs at sea, and preliminary
reports will be prepared during the field
program and summaries forwarded to
the operating institution’s shore facility
and to NSF weekly or more frequently.
MMVO observations will provide the
following information:
(1) The basis for decisions about
shutting down the GI guns.
(2) Information needed to estimate the
number of marine mammals potentially
‘‘taken by harassment.’’ These data will
be reported to NMFS and/or USFWS per
terms of MMPA authorizations..
(3) Data on the occurrence,
distribution, and activities of marine
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mammals in the area where the seismic
study is conducted.
(4) Data on the behavior and
movement patterns of marine mammals
seen at times with and without seismic
activity.
Mitigation
Mitigation and monitoring measures
proposed to be implemented for the
proposed seismic survey have been
developed and refined during previous
SIO and L-DEO seismic studies and
associated EAs, IHA applications, and
IHAs. The mitigation and monitoring
measures described herein represent a
combination of the procedures required
by past IHAs for other SIO and L-DEO
projects. The measures are described in
detail below.
Mitigation measures that are proposed
to be implemented include (1) vessel
speed or course alteration, provided that
doing so will not compromise
operational safety requirements, (2) GI
guns ramp up and shut down, and (3)
minimizing approach to slopes and
submarine canyons, if possible, because
of sensitivity of beaked whales. Two
other standard mitigation measures
airgun array power down are not
possible because only two, low-volume
GI guns will be used for the surveys.
Speed or Course Alteration – If a
marine mammal is detected outside the
EZ but is likely to enter it based on
relative movement of the vessel and the
animal, then if safety requirements
allow, the vessel speed and/or direct
course will be adjusted to minimize the
likelihood of the animal entering the EZ.
Major course and speed adjustments are
often impractical when towing long
seismic streamers and large source
arrays, but are possible in this case
because only two GI guns and a short PCable system with streamers will be
used. If the animal appears likely to
enter the EZ, further mitigative actions
will be taken, i.e. either further course
alterations or shut down of the airgun.
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.
Shut-down Procedures – If a marine
mammal is within or about to enter the
EZ for the two GI guns, it will be shut
down immediately. Following a shut
down, the GI guns activity will not
resume until the marine mammal is
outside the EZ for the full array. The
animal will be considered to have
cleared the EZ if it: (1) is visually
observed to have left the EZ; (2) has not
E:\FR\FM\23MYN1.SGM
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Federal Register / Vol. 73, No. 101 / Friday, May 23, 2008 / Notices
been seen within the EZ for 10 minutes
in the case of small odontocetes and
pinnipeds; or (3) has not been seen
within the EZ for 15 minutes in the case
of mysticetes and large odontocetes,
including sperm, pygmy sperm, dwarf
sperm, and beaked whales.
The 10– and 15–min periods specified
in (2) and (3), above, are shorter than
would be used in a large-source project
given the small 180 and 190 dB (rms)
radii for the two GI guns. GI gun
operations will be able to resume
following a shut-down during either the
day or night, as the relatively small
exclusion zone(s) will normally be
visible even at night (see section VIII of
UTIG’s application).
Minimize Approach to Slopes and
Submarine Canyons – Although
sensitivity of beaked whales to airguns
is not specifically known, they appear to
be sensitive to other sound sources (e.g.,
mid-frequency sonar; see section IV of
UTIG’s application). Beaked whales
tend to concentrate in continental slope
areas, and in areas where there are
submarine canyons. Avoidance of
airgun operations over or near
submarine canyons where practicable
has become a standard mitigation
measure, but there are no submarine
canyons within or near the study area.
Also, airgun operations are not planned
over slope sites during the proposed
survey.
Reporting
A report will be submitted to NMFS
within 90 days after the end of the
cruise. The report will describe the
operations that were conducted and
sightings of the marine mammals that
were detected 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, all
marine mammal and turtle sightings
(dates, times, locations, activities,
associated seismic survey activities).
The report will also include estimates of
the amount and nature of potential
‘‘take’’ of marine mammals by
harassment or in other ways.
dwashington3 on PRODPC61 with NOTICES
ESA
Under section 7 of the ESA, the NSF
has begun informal consultation on this
proposed seismic survey. NMFS will
also consult informally 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.
VerDate Aug<31>2005
15:34 May 22, 2008
Jkt 214001
National Environmental Policy Act
(NEPA)
NSF prepared an Environmental
Assessment (EA) of a Planned LowEnergy Marine Seismic Survey by the
Scripps Institution of Oceanography in
the Northeast Pacific Ocean, September
2007. NMFS adopted NSF’s 2007 EA
and will conducted a separate NEPA
analysis and prepare a Supplemental
EA, 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 Pacific
Ocean may result, at worst, in a
temporary modification in behavior
(Level B Harassment) of small numbers
of ten species of marine mammals.
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 to this proposed action as there
are no subsistence users within the
geographic area of the proposed project.
For reasons stated previously in this
document, this determination is
supported by: (1) the likelihood that,
given sufficient notice through
relatively slow ship speed, marine
mammals are expected to move away
from a noise source that is annoying
prior to its becoming potentially
injurious; (2) the fact that marine
mammals would have to be closer than
either 104 m (341.1 ft) in intermediate
depths or 69 m (226.3 ft) in deep water
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 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.
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30093
Proposed Authorization
As a result of these preliminary
determinations, NMFS proposes to issue
an IHA to UTIG for conducting a lowenergy seismic survey in the
northeastern Pacific Ocean during JuneJuly, 2008, provided the previously
mentioned mitigation, monitoring, and
reporting requirements are incorporated.
Dated: May 16, 2008.
James H. Lecky,
Director, Office of Protected Resources,
National Marine Fisheries Service.
[FR Doc. E8–11546 Filed 5–22–08; 8:45 am]
BILLING CODE 3510–22–S
COMMODITY FUTURES TRADING
COMMISSION
Energy Markets Advisory Committee
Meeting
This is to give notice that the
Commodity Futures Trading
Commission’s Energy Markets Advisory
Committee will conduct a public
meeting on Tuesday, June 10, 2008. The
meeting will take place in the first floor
hearing room of the Commission’s
Washington, DC headquarters, Three
Lafayette Centre, 1155 21st Street, NW.,
Washington, DC 20581 from 1 p.m. to
4:30 p.m. The purpose of the meeting is
to discuss energy market issues. The
meeting will be chaired by Walter L.
Lukken, who is Acting Chairman of the
Commission and Chairman of the
Energy Markets Advisory Committee.
The agenda will consist of the
following:
(1) Call to Order and Introduction;
(2) Current Market and Regulatory
Developments;
(3) Market Transparency;
(4) Energy Market Best Practices;
(5) Discussion of Future Meetings and
Topics;
(6) Adjournment.
The meeting is open to the public.
Any member of the public who wishes
to file a written statement with the
committee should mail a copy of the
statement to the attention of: Energy
Markets Advisory Committee, c/o
Acting Chairman Walter L. Lukken,
Commodity Futures Trading
Commission, Three Lafayette Centre,
1155 21st Street, NW., Washington, DC
20581, before the meeting. Members of
the public who wish to make oral
statements should inform Acting
Chairman Lukken in writing at the
foregoing address at least three business
days before the meeting. Reasonable
provision will be made, if time permits,
for oral presentations of no more than
five minutes each in duration.
E:\FR\FM\23MYN1.SGM
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Agencies
[Federal Register Volume 73, Number 101 (Friday, May 23, 2008)]
[Notices]
[Pages 30076-30093]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-11546]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XG64
Small Takes of Marine Mammals Incidental to Specified Activities;
Low-Energy Marine Seismic Survey in the Northeast Pacific Ocean, June-
July 2008
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental take authorization; request for
comments.
-----------------------------------------------------------------------
SUMMARY: NMFS has received an application from University of Texas,
Institute of Geophysics (UTIG) for an Incidental Harassment
Authorization (IHA) to take marine mammals incidental to conducting a
low-energy marine seismic survey in the Northeast Pacific Ocean during
June-July, 2008. Pursuant to the Marine Mammal Protection Act (MMPA),
NMFS is requesting comments on its proposal to issue an IHA to UTIG 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 June
23, 2008.
ADDRESSES: Comments on the application should be addressed to P.
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 PR1.0648XB70@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: Howard Goldstein or Ken Hollingshead,
Office of Protected Resources, NMFS, (301) 713-2289.
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 U.S. 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 March 4, 2008, NMFS received an application from UTIG for the
taking, by Level B harassment only, of several
[[Page 30077]]
species of marine mammals incidental to conducting, with research
funding from the National Science Foundation (NSF), a bathymetric and
seismic survey program approximately 100 km (approximately 62 mi) off
the Oregon coast in the Northeast Pacific Ocean during June-July, 2008.
The purpose of the research program is to investigate the methane vent
systems that exist offshore Oregon. These systems release methane by
active venting at the seafloor. They can also form relatively high
concentrations of methane hydrate in the sub seafloor, up to 150 m (492
ft) below the sea bottom. The goal is to image these systems in detail
to understand how vent structure directs methane from the subsurface to
be vented into the oceans, or potentially stored in the subsurface as
methane hydrate. Methane is a significant greenhouse gas, and methane
release from vents or from hydrate has a significant potential to
affect the Earth's climate. Hydrates are also a potentially significant
source of energy. Also included in the research is the use of a
multibeam echosounder and sub-bottom profiler.
Description of the Proposed Activity
The seismic survey will involve one vessel, the R/V Thomas G.
Thompson (Thompson), which is scheduled to depart from Seattle,
Washington on June 30, 2008 and return on July 19, 2008. The exact
dates of the activities may vary by a few days because of weather
conditions, scheduling, repositioning, streamer operations and
adjustments, GI airguns deployment, or the need to repeat some lines if
data quality is substandard. The proposed ultra-high resolution 3-
dimensional (3-D) seismic surveys around the methane vent systems of
Hydrate Ridge, will take place off the Oregon coast in the northeastern
Pacific Ocean. The overall area within which the seismic surveys will
occur is located between approximately 44[deg] and 45[deg] N. and
124.5[deg] and 126[deg] W (Figure 1 in the application). The surveys
will occur approximately 100 km (approximately 62 mi) offshore from
Oregon in water depths between approximately 650 and 1,200 m (2,132 and
3,936 ft), entirely within the Exclusive Economic Zone (EEZ) of the
U.S.
The seismic survey will image the subsurface structures that
control venting. The vent systems control whether the methane is
directly released into the ocean and atmosphere or stored in methane
hydrate. Methane hydrate storage has the potential for rapid
dissociation and release into the ocean or atmosphere. The subsurface
structure that will be imaged will determine the mechanisms involved in
methane venting. The results will be applicable to the numerous vent
systems that exist on continental margins worldwide. The data will also
be used to design observatories that can monitor and assess the methane
fluxes and mechanisms of methane release that operate on Hydrate Ridge.
The Thompson will deploy two low-energy Generator-Injector (GI)
airguns (guns) as an energy source (with a discharge volume of 40-60
in\3\ for each gun or a total of 80-120 in\3\) , and a P-Cable system.
The 12 m (39.5 ft) long P-Cable system is supplied by Northampton
Oceanographic Center in the U.K. The towed system will consist of at
least 12 streamers (and possibly up to 24) spaced approximately 12.5 m
(41 ft) apart and each containing 11 hydrophones, all summed to a
single channel. The energy to the GI guns is compressed air supplied by
compressors on board the source vessel. As the GI guns are towed along
the survey lines, the P-Cable system will receive the returning
acoustic signals.
The seismic program will consist of three survey grids: two of the
surveys each cover a 15 km2 area and the third covers a 25 km\2\ (see
Figure 1 in UTIG's application). The line spacing within the three
survey grids will either be 75 m (246 ft) (if 12 streamers are used) or
150 m (492 ft) (if 24 streamers are used). The total line km to be
surveyed in the grids at the 75 m spacing is 975 km (605.8 mi),
including turns. Water depths at the seismic survey locations range
from 650 to 1,200 m (2132 to 3936 ft). Most (92 percent) of the survey
will take place over intermediate (100-1,000 m) water depths; the
remaining 8 percent will be in water deeper than 1,000 m. If time
permits, an additional 300 line km will be surveyed along the outside
edges of the three grids. The GI guns are expected to operate for a
total of approximately 150 hours during the cruise. 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 two GI guns and P-cable
system, a Simrad EM300 30 kHz multibeam echosounder, and a Knudsen 12
kHz 320BR sub-bottom profiler will be used during the proposed cruise.
Vessel Specifications
The Thompson has a length of 83.5 m (274 ft), a beam of 16 m (52.5
ft), and a maximum draft of 5.8 m (19 ft). The ship is powered by twin
360[deg]-azimuth stern thrusters a single 3,000-hp DC motor and a
water-jet bow thruster powered by a 1,600-hp motor. The motors are
driven by up to three 1,500-kW and three 715-kW generators; normal
operations use two 1,500-kW and one 750-kW generator, but this changes
with ship speed, sea state, and other variables. An operation speed of
6.5 km/h (3.5 knots) will be used during seismic acquisition. When not
towing seismic survey gear, the Thompson cruises at 22.2 km/h (12
knots) and has a maximum speed of 26.9 km/h (14.5 knots). It has a
normal operating range of approximately 24,400 km (8,264 mi).
Acoustic Source Specifications
Seismic Airguns
The vessel Thompson will tow two GI guns and a P-Cable system of 12
to 24, 12 m long streamers containing hydrophones along predetermined
survey grids. Seismic pulses will be emitted at intervals of 3.5 s,
which corresponds to a shot interval of approximately 6.3 m (20.7 ft)
at a speed of 3.5 knots (6.5 km/h). The generator chamber of a GI gun,
the one responsible for introducing the sound pulse into the ocean, is
40-60 in3. The second injector chamber (40-60 in3) injects air into the
previously-generated bubble to maintain its shape and does not
introduce more sound into the water. The two 40-60 in3 GI guns will be
towed 29 m (95.1 ft) behind the Thompson, at a depth of 1.5-3 m (4.9-
9.8 ft). The dominant frequency components are 0-188 Hz.
The sound pressure field of two 105 in\3\ GI guns has been modeled
by the Lamont-Doherty Earth Observatory (L-DEO) of Columbia University
in relation to distance and direction from the GI guns. The model does
not allow for bottom interactions and is most directly applicable to
close distances and/or deep water. Because the L-DEO model is for a
pair of larger GI guns with a total discharge of up to 210 in\3\, the
values overestimate the distances for two GI guns with a discharge of
up to 120 in3, as planned for use during the proposed study. This
source, which is directed downward, was found to have an output (0-
peak) of 237 dB re 1 microPam.
The root mean square (rms) 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 rms decibels
referred to in biological literature. A measured received level of 160
dB rms in the far field would
[[Page 30078]]
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.
Sub-bottom Profiler
The Thompson will utilize a Simrad EM300 30-kHz Multibeam
Echosounder (MBES) as the primary bottom-mapping echosounder during the
cruise. The Simrad EM300 transducer is hull-mounted within a transducer
pod that is located midship. The system's normal operating frequency is
approximately 30 kHz. The transmit fan-beam is split into either three
or nine narrower beam sectors with independent active steering to
correct for vessel yaw. Angular coverage is 36 degrees (in Extra Deep
Mode, for use in water depths 3,000 to 6,000 m) or 150 degrees (in
shallower water). The total angular coverage of 36 or 150 degrees
consists of the 3 or 9 beams transmitted at slightly different
frequencies. The sectors are frequency coded between 30 and 34 kHz and
they are transmitted sequentially at each ping. Except in very deep
water where the total beam is 36 x 1, the composite fan beam will
overlap slightly if the vessel yaw is less than the fore-aft width of
the beam (1,2, or 4, respectively). Achievable swath width on a flat
bottom will normally be approximately 5x the water depth. The maximum
source level is 237 dB re 1 microPam (rms) (Hammerstand, 2005).
In deep water (500-3,000 m) a pulse length of 5 ms is normally used. At
intermediate depths (100-1,000 m), a pulse length of 2 ms is used, and
in shallow water (<300 m), a pulse length of 0.7 ms is used. The ping
rate is mainly limited by the round trip travel time in the water up to
a ping rate of 10 pings/s in shallow water.
The Thompson will also utilize the Knudsen Engineering Model 320BR
sub-bottom profiler, which is a dual-frequency echosounder designed to
operate at 3.5 and/or 12 kHz. It is used 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 12 kHz transducer (EDO 323B) or a 3.5 kHz array of 16 ORE 137D
transducers in a 4 x 4 arrangement. The maximum power output of the
320BR is 10 kilowatts for the 3.5 kHz section and 2 kilowatts for the
12 kHz section.
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 the interval is
estimated to be every 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 one 45-in\3\ GI gun, in relation to
distance and direction from the airgun(s). 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
gun 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 8, 23,
and 220 m (26.2, 75.5, and 721.8 ft), respectively and 12, 35, and 330
m (39.4, 115, and 1,082.7 ft), respectively for intermediate water
depths (100-1000m, 328-3,280 ft). Because the model results are for a
2.5-m (8.2-ft) tow depth, the above distances slightly underestimate
the distances for the 45-in\3\ GI gun towed at 4-m (13-ft) depth.
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 100-1,000 m (328-
3,280 ft) and <100 m (328 ft). The proposed survey will occur in depths
650-1,200 m (2,132-3,936 ft), so the correction factors for the latter
are not relevant here.
The empirical data indicate that, for deep water (>1,000 m, 3,280
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 69 m and 20 m (226.3 and 65.6 ft), respectively.
Empirical measurements were not conducted for intermediate depths
(100-1,000 m, 328-3,280 ft). On the expectation that results will be
intermediate between those from shallow and deep water, a 1.5x
correction factor is applied to the estimates provided by the model for
deep water situations. This is the same factor that was applied to the
model estimates during L-DEO cruises in 2003. The assumed 180- and 190-
dB radii in intermediate-depth water are 104 m and 30 m (341.1 and 98.4
ft), respectively.
The GI guns will be shut down immediately when cetaceans or
pinnipeds are detected within or about to enter the measured 180-dB
(rms) or 190-dB (rms) radius, respectively.
Description of Marine Mammals in the Activity Area
Thirty-two marine mammal species, including 19 odontocete (dolphins
and small and large toothed whales) species, seven mysticete (baleen
whales) species, five pinniped species, and the sea otter,
[[Page 30079]]
may occur or have been documented to occur in the marine waters off
Oregon and Washington, excluding extralimital sightings or strandings
(Table 1 here). Six of the species that may occur in the project area
are listed under the U.S. Endangered Species Act (ESA) as endangered,
including sperm, humpback, blue, fin, sei, and North Pacific right
whales. In addition, the southern resident killer whale stock is also
listed as endangered, but is unlikely to be seen in offshore waters of
Oregon. The threatened Steller sea lion could also occur in the project
area. However, the threatened northern sea otter is only known to occur
in coastal waters and is not expected in the project area (the sea
otter is under the jurisdiction of the U.S. Fish and Wildlife Service.
Gray whales are also not expected in the project area because their
occurrence off Oregon is limited to very shallow, coastal waters. The
California sea lion, Steller sea lion, and harbor seal are also mainly
coastal and are not expected at the survey locations. Information on
habitat and abundance of the species that may occur in the study area
are given in Table 1 below. Vagrant ringed seals, hooded seals, and
ribbon seals have been sighted or stranded on the coast of California
(see Mead, 1981; Reeves et al., 2002) and presumably passed through
Oregon waters. A vagrant beluga was seen off the coast of Washington
(Reeves et al., 2002).
The six species of marine mammals expected to be most common in the
deep pelagic or slope waters of the project area, where most of the
survey sites are located, include the Pacific white-sided dolphin,
northern right whale dolphin, Risso's dolphin, short-beaked common
dolphin, Dall's porpoise, and northern fur seal (Green et al., 1992,
1993; Buchanan et al., 2001; Barlow, 2003; Carretta et al., 2006).
The sperm, pygmy sperm, mesoplodont species, Baird's beaked, and
Cuvier's beaked whales and the northern elephant seal are considered
pelagic species, but are generally uncommon in the waters near the
survey area. Additional information regarding the distribution of these
species expected to be found in the project area and how the estimated
densities were calculated may be found in UTIG's application.
----------------------------------------------------------------------------------------------------------------
Species Habitat Abundance\1\ Rqstd Take
----------------------------------------------------------------------------------------------------------------
Mysticetes ............................... .................... ..................
North Pacific right whale (Eubalaena Inshore, occasionally offshore N.A.\2\ 0
japonica) *
----------------------------------------------------------------------------------------------------------------
Humpback whale (Megaptera Mainly nearshore waters and 1391 1
novaeangliae) * banks
----------------------------------------------------------------------------------------------------------------
Minke whale (Balaenoptera Pelagic and coastal 1015 1
acutorostrata)
----------------------------------------------------------------------------------------------------------------
Sei whale (Balaenoptera borealis) * Primarily offshore, pelagic 56 0
----------------------------------------------------------------------------------------------------------------
Fin whale (Balaenoptera physalus) * Continental slope, mostly 3279 1
pelagic
----------------------------------------------------------------------------------------------------------------
Blue whale (Balaenoptera musculus) * Pelagic and coastal 1744 0
----------------------------------------------------------------------------------------------------------------
Odontocetes ............................... .................... ..................
Sperm whale (Physeter macrocephalus) Usually pelagic and deep seas 1233 2
*
----------------------------------------------------------------------------------------------------------------
Pygmy sperm whale (Kogia breviceps) Deep waters off the shelf 247 2
----------------------------------------------------------------------------------------------------------------
Dwarf sperm whale (Kogia sima) Deep waters off the shelf N.A. 0
----------------------------------------------------------------------------------------------------------------
Cuvier's beaked whale (Ziphius Pelagic 1884 0
cavirostris)
----------------------------------------------------------------------------------------------------------------
Baird's beaked whale (Berardius Pelagic 228 1
bairdii)
----------------------------------------------------------------------------------------------------------------
Blainville's beaked whale (Mesoplodon Slope, offshore 1247 \3\ 0
densirostris)
----------------------------------------------------------------------------------------------------------------
Hubb's beaked whale (Mesoplodon Slope, offshore 1247 \3\ 0
carlhubbsi)
----------------------------------------------------------------------------------------------------------------
Stejneger's beaked whale (Mesoplodon Slope, offshore 1247 \3\ 0
stejnegeri)
----------------------------------------------------------------------------------------------------------------
Mesoplodon sp. (Unidentified) Slope, offshore 1247 1
----------------------------------------------------------------------------------------------------------------
Offshore bottlenose dolphin (Tursiops Offshore, slope 5,065 0
truncatus)
----------------------------------------------------------------------------------------------------------------
Striped dolphin (Stenella Off continental shelf 13,934 0
coeruleoalba)
----------------------------------------------------------------------------------------------------------------
Short-beaked common dolphin Shelf and pelagic, seamounts 449,846 7
(Delphinus delphis)
----------------------------------------------------------------------------------------------------------------
Pacific white-sided dolphin Offshore, slope 59,274 6
(Lagenorhynchus obliquidens)
----------------------------------------------------------------------------------------------------------------
Northern right whale dolphin Slope, offshore waters 20,362 5
(Lissodelphis borealis)
----------------------------------------------------------------------------------------------------------------
Risso's dolphin (Grampus griseus) Shelf, slope, seamounts 16,066 3
----------------------------------------------------------------------------------------------------------------
False killer whale (Pseudorca Pelagic, occasionally inshore N.A. 0
crassidens)
----------------------------------------------------------------------------------------------------------------
Killer whale (Orcinus orca) Widely distributed 466 (Offshore) 1
----------------------------------------------------------------------------------------------------------------
[[Page 30080]]
Short-finned pilot whale Mostly pelagic, high-relief 304 0
(Globicephala macrorhynchus) topography
----------------------------------------------------------------------------------------------------------------
Harbor porpoise (Phocoena phocoena) Coastal and inland waters 39,586 (OR/WA) 0
----------------------------------------------------------------------------------------------------------------
Dall's porpoise (Phocoenoides dalli) Shelf, slope, offshore 99,517 47
----------------------------------------------------------------------------------------------------------------
Pinnipeds ............................... .................... ..................
Northern fur seal (Callorhinus Pelagic, offshore 688,028 \2\ 19
ursinus)
----------------------------------------------------------------------------------------------------------------
California sea lion (Zalophus Coastal, shelf 237,000-244,000 NA
californianus californianus)
----------------------------------------------------------------------------------------------------------------
Northern elephant seal (Mirounga Coastal, pelagic when migrating 101,000 (CA) 2
angustirostris)
----------------------------------------------------------------------------------------------------------------
Table 1. Species expected to be encountered (and potentially harassed) during UTIG's NE Pacific Ocean cruise.
N.A. B Data not available or species status was not assessed.
* Species are listed as threatened or endangered under the Endangered Species Act.
\1\ Abundance given for U.S., Eastern North Pacific, or California/Oregon/Washington Stock, whichever is
included in the 2005 U.S. Pacific Marine Mammal Stock Assessments (Carretta et al. 2006), unless otherwise
stated.
\2\ Angliss and Outlaw (2005).
\3\ All mesoplodont whales
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 or non-
auditory physical or physiological effects (Richardson et al., 1995;
Gordon et al., 2004). Given the small size of the GI guns planned for
the proposed 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 or any significant non-auditory physical
or physiological effects. 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 UTIG'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 two GI guns planned for use in the
proposed project.
Numerous other 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 UTIG's application). That is
often true even in cases when the pulsed sounds appear to 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, low-energy airgun source planned for use in this project, NMFS
expects mammals to tolerate being closer to this source than for a
larger airgun source typical of most seismic surveys. Mysticetes,
odontocetes, pinnipeds and sea otters have all been seen commonly by
observers aboard vessels conducting small-source seismic surveys,
indicating some degree of tolerance of sounds from small airgun sources
(e.g., Calambokidis et al., 2002; Haley and Koski, 2004; Holst et al.,
2005a; Ireland et al., 2005; MacLean and Koski, 2005; see also ``site
survey'' portions of Stone, 2003 and Stone and Tasker, 2006).
Masking
Obscuring of sounds of interest by interfering sounds, generally at
similar frequencies, is known as 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 matter. 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;
Smultea 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). Similar reactions have also been shown during
recent work in the Gulf of Mexico (Tyack et al., 2003; Smultea et al.,
2004). 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 airgun to be used here. Dolphins and
porpoises are commonly heard calling while airguns are operating
(Gordon et al., 2004; Smultea et al., 2004; Holst et al., 2005a,b).
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 UTIG's application.
Disturbance Reactions
Disturbance includes a variety of effects, including subtle changes
in behavior, more conspicuous changes in activities, and displacement.
Reactions to sound, if any, depend on species, state of maturity,
experience, current activity, reproductive state, time of day, and many
other factors (Richardson et al., 1995; Wartzok et al., 2004; Southall
et al., 2007). If a marine mammal responds to an underwater sound by
changing its behavior or moving a small
[[Page 30081]]
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 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 UTIG'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 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 UTIG'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 0.22 or 0.33 km (0.14 or 0.21 mi), as compared with
several kilometers when a large array of airguns is operating.
Responses of humpback whales to seismic surveys have been studied
during migration and on the summer feeding grounds, and there has also
been discussion of effects on the Brazilian wintering grounds. McCauley
et al. (1998, 2000) studied the responses of humpback whales off
Western Australia to a full-scale seismic survey with a 16-airgun,
2,678-in\3\ array, and to a single 20-in\3\ airgun with a source level
of 227 dB re 1 microPa m. McCauley et al. (1998) documented that
avoidance reactions began at 5-8 km (3.1-5 mi) from the array, and that
those reactions kept most pods approximately 3-4 km (1.9-2.5 mi) from
the operating seismic boat. McCauley et al. (2000) noted localized
displacement during migration of 4-5 km (2.5-3.1 mi) by traveling pods
and 7-12 km (4.3-7.5 mi) by cow-calf pairs. Avoidance distances with
respect to the single airgun were smaller but consistent with the
results from the full array in terms of received sound levels. Mean
avoidance distance from the airgun corresponded to a received sound
level of 140 dB re 1 microPa (rms); that was the level at which
humpbacks started to show avoidance reactions to an approaching airgun.
The standoff range, i.e., the closest point of approach of the whales
to the airgun, corresponded to a received level of 143 dB re 1 microPa
(rms). The initial avoidance response generally occurred at distances
of 5-8 km (3.1-5 mi) from the airgun array and 2 km (1.2 mi) from the
single airgun. However, some individual humpback whales, especially
males, approached within distances of 100-400 m (328-1,312 ft), where
the maximum received level was 179 dB re 1 microPa (rms).
Humpback whales on their summer feeding grounds in southeast Alaska
did not exhibit persistent avoidance when exposed to seismic pulses
from a 1.64-L (100 in\3\) airgun (Malme et al., 1985). Some humpbacks
seemed ``startled'' at received levels of 150-169 dB re 1 microPa on an
approximate rms basis. Malme et al. (1985) conclude 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).
It has been suggested that South Atlantic humpback whales wintering
off Brazil may be displaced or even strand upon exposure to seismic
surveys (Engel et al., 2004). The evidence for this was circumstantial,
subject to alternative explanations (IAGC 2004), and not consistent
with results from direct studies of humpbacks exposed to seismic
surveys in other areas and seasons. After allowance for data from
subsequent years, there was ``no observable direct correlation''
between strandings and seismic surveys (IWC 2007:236).
Results from bowhead whales show that responsiveness of baleen
whales to seismic surveys can be quite variable depending on the
activity (migrating vs. feeding) of the whales. Bowhead whales
migrating west across the Alaskan Beaufort Sea in autumn, in
particular, are unusually responsive, with substantial avoidance
occurring out to distances of 20 30 km (12.4-18.6 mi) from a medium-
sized airgun source, where received sound levels were on the order of
130 dB re 1 microPa (rms) (Miller et al., 1999; Richardson et al.,
1999). However, more recent research on bowhead whales (Miller et al.,
2005a) corroborates earlier evidence that, during the summer feeding
season, bowheads are not as sensitive to seismic sources. In summer,
bowheads typically begin to show avoidance reactions at a received
level of about 160-170 dB re 1 microPa (rms) (Richardson et al., 1986;
Ljungblad et al., 1988; Miller et al., 1999). There are no data on the
reactions of wintering bowhead whales to seismic surveys. See Appendix
A (e) of UTIG's application for more information regarding bowhead
whale reactions to airguns.
Reactions of migrating and feeding (but not wintering) gray whales
to seismic surveys have been studied. Malme et al. (1986, 1988) studied
the responses of feeding Eastern Pacific gray whales to pulses from a
single 100 in\3\ airgun off St. Lawrence Island in the
[[Page 30082]]
northern Bering Sea. Malme et al. (1986, 1988) 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 and on observations of Western Pacific gray whales feeding off
Sakhalin Island, Russia (Johnson et al., 2007).
Various species of Balaenoptera (blue, fin, sei, and minke whales)
have occasionally been reported in areas ensonified by airgun pulses.
Sightings by observers on seismic vessels off the U.K. from 1997 to
2000 suggest that, at times of good sightability, numbers of rorquals
seen are similar when airguns are shooting and not shooting (Stone,
2003). Although individual species did not show any significant
displacement in relation to seismic activity, all baleen whales
combined were found to remain significantly further from the airguns
during shooting compared with periods without shooting (Stone, 2003;
Stone and Tasker, 2006). In a study off Nova Scotia, Moulton and Miller
(2005) found little or no difference in sighting rates and initial
sighting distances of balaenopterid whales when airguns were operating
vs. silent. However, there were indications that these whales were more
likely to be moving away when seen during airgun operations.
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, a systematic study on sperm
whales has been done (Jochens and Biggs, 2003; Tyack et al., 2003;
Miller et al., 2006), and there is an increasing amount of information
about responses of various odontocetes to seismic surveys based on
monitoring studies (Stone, 2003; Smultea et al., 2004; Bain and
Williams, 2006; Holst et al., 2006; Stone and Tasker, 2006; Moulton and
Miller, 2005).
Seismic operators and marine mammal observers 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 (Goold,
1996; Calambokidis and Osmek, 1998; Stone, 2003). In most cases, the
avoidance radii for delphinids appear to be small, on the order of 1 km
(0.62 mi) or less.
The beluga may be a species that (at least at times) shows long-
distance avoidance of seismic vessels. Aerial surveys during seismic
operations in the southeastern Beaufort Sea recorded much lower
sighting rates of beluga whales within 10-20 km (6.2-12.4 mi) of an
active seismic vessel. These results were consistent with the low
number of beluga sightings reported by observers aboard the seismic
vessel, suggesting that some belugas might be avoiding the seismic
operations at distances of 10-20 km (6.2-12.4 mi) (Miller et al.,
2005a). 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, 2005; Finneran and Schlundt, 2004).
However, the animals tolerated high received levels of sound (pk-pk
level >200 dB re 1 microPa) before exhibiting aversive behaviors.
Results for porpoises depend on species. Dall's porpoises seem
relatively tolerant of airgun operations (MacLean and Koski, 2005; Bain
and Williams, 2006), whereas the limited available data suggest that
harbor porpoises show stronger avoidance (Stone, 2003; Bain and
Williams, 2006; Stone and Tasker, 2006). This apparent difference in
responsiveness of these two porpoise species is consistent with their
relative responsiveness to boat traffic in general (Richardson et al.,
1995; Southall et al., 2007).
Most studies of sperm whales exposed to airgun sounds indicate that
this species shows considerable tolerance of airgun pulses. In most
cases, the whales do not show strong avoidance, and they continue to
call (see Appendix A of UTIG's application for review). However,
controlled exposure experiments in the Gulf of Mexico indicate that
foraging effort is apparently somewhat reduced upon exposure to airgun
pulses from a seismic vessel operating in the area, and there may be a
delay in diving to foraging depth.
There are no specific data on the behavioral reactions of beaked
whales to seismic surveys. Most beaked whales tend to avoid approaching
vessels of other types (Wursig et al., 1998). They may also dive for an
extended period when approached by a vessel (Kasuya, 1986). It is
likely that these beaked whales would normally show strong avoidance of
an approaching seismic vessel, but this has not been documented
explicitly.Odontocete reactions to large arrays of airguns are variable
and, at least for delphinids and some porpoises, seem to be confined to
a smaller radius than has been observed for mysticetes (see Appendix A
of UTIG's application for more information). Behavioral reactions of
most odontocetes to the small GI gun source to be used here are
expected to be very localized.
Pinnipeds - Pinnipeds are not likely to show a strong avoidance
reaction to the two GI guns 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 UTIG's application).
Ringed seals frequently do not avoid the area within a few hundred
meters of operating airgun arrays (Harris et al., 2001; Moulton and
Lawson, 2002; Miller et al., 2005a). However, initial telemetry work
suggests that avoidance and other behavioral reactions by two other
species of seals to small airgun sources may at times be stronger than
evident to date from visual studies of pinniped reactions to airguns
(Thompson et al., 1998). Even if reactions of any pinnipeds that might
be encountered in the present study area are as strong as those evident
in the telemetry study, reactions are expected to be confined to
relatively small distances and durations, with no long-
[[Page 30083]]
term effects on pinniped individuals or populations.
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 UTIG'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 (NMFS, 2000). 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 UTIG'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 scientific data
on TTS, the expected offset between the TTS and permanent threshold
shift (PTS) thresholds, differences in the acoustic frequencies to
which different marine mammal groups are sensitive, and other relevant
factors.
Because of the small size of the airgun source in this project (two
40-60 in\3\ GI gun), alongwith 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
GI guns (and multibeam echosounder and sub-bottom profiler), 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,
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. 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, 2005). Given the
available data, the received level of a single seismic pulse (with no
frequency weighting) might need to be approximately 186 dB re 1
microPa\2\s (i.e., 186 dB SEL or approximately 221-226 dB pk-
pk) in order to produce brief, mild TTS. Exposure to several strong
seismic pulses that each have received levels near 175-180 dB SEL 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. The distances from the Thompson's GI guns at which the received
energy level (per pulse) would be expected to be [gteqt]175-180 dB SEL
are the distances shown in the 190 dB re 1 microPa (rms) column in
Table 1 of UTIG's application (given that the rms level is
approximately 10-15 dB higher than the SEL value for the same pulse).
Seismic pulses with received energy levels [gteqt]175-180 dB SEL (190
dB re 1 microPa (rms)) are expected to be restricted to radii no more
than 69-104 m (226.3-341.1 ft) around the two GI guns. The specific
radius depends on the depth of the water. For an odontocete closer to
the surface, the maximum radius with [gteqt]175-180 dB SEL or
[gteqt]190 dB re 1 microPa (rms) would be smaller. Such levels would be
limited to distances within tens of meters of the small GI guns source
to be used in this project.
For baleen whales, direct or indirect data do not exist on levels
or properties of sound thatare required to induce TTS. The frequencies
to which baleen whales are most sensitive are lower than those to which
odontocetes are most sensitive, and natural background noise levels at
those low frequencies tend to be higher. As a result, auditory
thresholds of baleen whales within their frequency band of best hearing
are believed to be higher (less sensitive) than are those of
odontocetes at their best frequencies (Clark and Ellison, 2004). From
this, it is suspected that received levels causing TTS onset may also
be higher in baleen whales. In any event, no cases of TTS are expected
given three considerations: (1) the low abundance of baleen whales
expected in the planned study areas; (2) the strong likelihood that
baleen whales would avoid the approaching airguns (or vessel) before
being exposed to levels high enough for there to be any possibility of
TTS; and (3) the mitigation measures that are proposed to be
implemented.
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 suggests that some pinnipeds
may incur TTS at somewhat lower received levels than do small
odontocetes exposed for similar durations (Kastak et al., 1999, 2005;
Ketten et al., 2001; cf. Au et al., 2000). The TTS threshold for pulsed
sounds has been indirectly estimated as being an SEL of about 171 dB re
microPa\2\s (Southall et al., 2007), which would be equivalent
to about 181-186 dB re 1 microPa (rms). Corresponding values for
California sea lions and northern elephant seals are likely to be
higher (Kastak et al., 2005).
To avoid injury, NMFS has determined that cetaceans and pinnipeds
should not be exposed to
[[Page 30084]]
pulsed underwater noise at received levels exceeding, respectively, 180
and 190 dB re 1 microPa (rms). Those sound levels were not considered
to be the levels above which TTS might occur. Rather, they were the
received levels above which, in the view of a panel of bioacoustics
specialists convened by NMFS before TTS measurements for marine mammals
started to become available, one could not be certain that there would
be no injurious effects, auditory or otherwise, to marine mammals. As
summarized above, data that are now available imply that TTS is
unlikely to occur unless odontocetes (and probably mysticetes as well)
are exposed to airgun pulses stronger than 180 dB re 1 microPa (rms).
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 at
least several decibels above that inducing mild TTS if the animal were
exposed to strong sound pulses with rapid rise time (see Appendix A (f)
of UTIG's application). The specific difference between the PTS and TTS
thresholds has not been measured for marine mammals exposed to any
sound type. However, based on data from terrestrial mammals, a
precautionary assumption is that the PTS threshold for impulse sounds
(such as airgun pulses as received close to the source) is at least 6
dB higher than the TTS threshold on a peak-pressure basis and probably
more than 6 dB.
On an SEL basis, Southall et al. (2007) estimate that received
levels would need to exceed the TTS threshold by at least 15 dB for
there to be risk of PTS. Thus, for cetaceans they estimate that the PTS
threshold might be an SEL of about 198 dB re 1 microPa\2\.s. Additional
assumptions had to be made to derive a corresponding estimate for
pinnipeds. Southall et al. (2007) estimate that the PTS threshold could
be an SEL of about 186 dB re 1 microPa\2\s in the harbor seal;
for the California sea lion and northern elephant seal the PTS
threshold would probably be higher. Southall et al. (2007) also not
that, regardless of the SEL, there is concern about the possibility of
PTS if a cetacean or pinniped received one or more pulses with peak
pressure exceeding 230 or 218 dB 1 microPa (peak).
In the proposed project employing two 40 to 60-in\3\ GI guns,
marine mammals are highly 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 tens of meters of the GI guns 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 GI guns 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 the GI guns for a period longer
than the inter-pulse interval. Baleen whales generally avoid the
immediate area around operating seismic vessels, as do some other
marine mammals and sea turtles. The planned monitoring and mitigation
measures, including visual monitoring and shut downs of the GI guns
when mammals are seen within or about to enter the ``safety radii'' or
exclusion zone (EZ), 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. However, studies examining such effects are limited.
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, when the sound is strongly channeled with less-than-
normal propagation loss, or when dispersal of the animals is
constrained by shorelines, shallows, etc. Airgun pulses, because of
their brevity and intermittence, are less likely to trigger resonance
or bubble formation than are more prolonged sounds. It is doubtful that
any single marine mammal would be exposed to strong seismic sounds for
time periods long enough to induce physiological stress.
Until recently, it was assumed that diving marine mammals are not
subject to the bends or air embolism. This possibility was first
explored at a workshop (Gentry [ed.], 2002) 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 bubble
formation in tissues caused by exposure to noise from naval sonar.
However, this link could not be confirmed. Jepson et al. (2003) first
suggested a possible link between mid-frequency sonar activity and
acute chronic tissue damage that results from the formation in vivo of
gas bubbles, based on the beaked whale stranding in the Canary Islands
in 2002 during naval exercises. Fernandez et al. (2005a) showed those
beaked whales did indeed have gas bubble-associated lesions, as well as
fat embolisms. Fernandez et al. (2005b) also found evidence of fat
embolism in three beaked whales that stranded 100 km (62 mi) north of
the Canaries in 2004 during naval exercises. Examinations of several
other stranded species have also revealed evidence of gas and fat
embolisms (Arbelo et al., 2005; Jepson et al., 2005a; Mendez et al.,
2005). Most of the afflicted species were deep divers. There is
speculation that gas and fat embolisms may occur if cetaceans ascend
unusually quickly when exposed to aversive sounds, or if sound in the
environment causes the destablization of existing bubble nuclei
(Potter, 2004; Arbelo et al., 2005; Fernandez et al., 2005a; Jepson et
al., 2005b; Cox et al., 2006). Even if gas and fat embolisms can occur
during exposure to mid-frequency sonar, there is no evidence that that
type of effect occurs in response to airgun sounds.
In general, little is known about the potential for seismic survey
sounds to cause auditory imp