Takes of Marine Mammals Incidental to Specified Activities; Taking Marine Mammals Incidental to Buccaneer Energy Drilling Activities in Upper Cook Inlet, 2014, 19251-19280 [2014-07601]
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Vol. 79
Monday,
No. 66
April 7, 2014
Part III
Department of Commerce
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National Oceanic and Atmospheric Administration
Takes of Marine Mammals Incidental to Specified Activities; Taking Marine
Mammals Incidental to Buccaneer Energy Drilling Activities in Upper Cook
Inlet, 2014; Notice
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Federal Register / Vol. 79, No. 66 / Monday, April 7, 2014 / Notices
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XD165
Takes of Marine Mammals Incidental to
Specified Activities; Taking Marine
Mammals Incidental to Buccaneer
Energy Drilling Activities in Upper
Cook Inlet, 2014
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; proposed incidental
harassment authorization; request for
comments.
AGENCY:
NMFS has received an
application from Buccaneer Alaska
Operation, LLC (Buccaneer) for an
Incidental Harassment Authorization
(IHA) to take marine mammals, by
harassment, incidental to conducting a
multi-well offshore exploratory drilling
program in upper Cook Inlet during the
2014 open water season. Pursuant to the
Marine Mammal Protection Act
(MMPA), NMFS is requesting comments
on its proposal to issue an IHA to
Buccaneer to incidentally take, by Level
B harassment only, marine mammals
during the specified activity.
DATES: Comments and information must
be received no later than May 7, 2014.
ADDRESSES: Comments on the
application should be addressed to Jolie
Harrison, Supervisor, Incidental Take
Program, Permits and Conservation
Division, Office of Protected Resources,
National Marine Fisheries Service, 1315
East-West Highway, Silver Spring, MD
20910. The mailbox address for
providing email comments is
ITP.Nachman@noaa.gov. NMFS is not
responsible for email comments sent to
addresses other than the one provided
here. Comments sent via email,
including all attachments, must not
exceed a 25-megabyte file size.
Instructions: All comments received
are a part of the public record and will
generally be posted to https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm without change. All
Personal Identifying Information (e.g.,
name, address) voluntarily submitted by
the commenter may be publicly
accessible. Do not submit Confidential
Business Information or otherwise
sensitive or protected information.
An electronic 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
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SUMMARY:
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(see FOR FURTHER INFORMATION CONTACT),
or visiting the internet at: https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm. Documents cited in this
notice may also be viewed, by
appointment, during regular business
hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT:
Candace Nachman, Office of Protected
Resources, NMFS, (301) 427–8401.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the
MMPA (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce to allow,
upon request, the incidental, but not
intentional, taking of small numbers 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 for incidental takings
shall be granted if NMFS finds that the
taking will have a negligible impact on
the species or stock(s), will not have an
unmitigable adverse impact on the
availability of the species or stock(s) for
subsistence uses (where relevant), and if
the permissible methods of taking, other
means of effecting the least practicable
impact on the species or stock and its
habitat, 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.’’
Except with respect to certain
activities not pertinent here, the MMPA
defines ‘‘harassment’’ as: ‘‘Any act of
pursuit, torment, or annoyance which (i)
has the potential to injure a marine
mammal or marine mammal stock in the
wild [Level A harassment]; or (ii) has
the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment].’’
Summary of Request
On August 30, 2013, NMFS received
an IHA application from Buccaneer for
the taking of marine mammals
incidental to a multi-well, multi-year
offshore exploratory drilling program in
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upper Cook Inlet during the 2014 open
water season (typically mid-April
through October). This request was for
1-year of the program. NMFS
determined that the application was
adequate and complete on November
25, 2013. However, on February 13,
2014, Buccaneer informed NMFS that a
portion of the activity contained in the
application is no longer proposed. As
described in more detail below,
Buccaneer proposes to drill four wells
instead of six during this multi-year
program.
Buccaneer proposes to drill up to four
exploratory wells during this multi-year
program and will likely drill up to two
wells each year at locations in upper
Cook Inlet. The proposed activity for
this IHA (if issued) would occur during
the open water months in 2014, which
is typically from April through October.
The following specific aspects of the
proposed activities are likely to result in
the take of marine mammals: Driving of
the conductor pipe; exploratory drilling;
towing of the jack-up drill rig; and
vertical seismic profiling (VSP). Take,
by Level B harassment only, of six
marine mammal species is anticipated
to result from the specified activity.
Description of the Specified Activity
Overview
Buccaneer proposes to conduct
exploratory drilling operations at
multiple well sites in upper Cook Inlet
during the 2014 summer and fall open
water (ice-free) season, using the
Endeavour-Spirit of Independence
(Endeavour) jack-up drill rig. The rig
will be towed between drilling locations
and winter moorage by ocean-going
tugs. The activities of relevance to this
IHA request include: Mobilization and
demobilization of the drill rig to and
from the well locations at the start and
end of the season; driving of the
conductor pipe; exploratory drilling;
and VSP seismic operations. Buccaneer
proposes to utilize both helicopters and
vessels to conduct resupply, crew
change, and other logistics during the
exploratory drilling program.
Dates and Duration
The 2014 exploratory drilling program
(which is the subject of this IHA
request) would occur during the 2014
open water season (April 15 through
October 31). Drilling will take
approximately 30 to 75 days per well,
and well testing will take another 7 to
15 days per well. Buccaneer proposes to
drill at up to two well locations in 2014
in upper Cook Inlet. During this time
period, conductor pipe driving would
only occur for a period of 1 to 3 days
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at each location, and VSP seismic
operations would only occur for a
period of less than 1 to 2 days at each
location. The rig tows will take
approximately 2 days to complete
during mobilization and demobilization
from upper Cook Inlet, and the shorter
tow between the two well locations in
upper Cook Inlet will take a few hours.
This IHA (if issued) would be effective
from date of issuance through October
31, 2014.
Specified Geographic Region
Buccaneer’s proposed program would
occur at up to two of four possible well
locations in upper Cook Inlet. The
Tyonek Deep well sites are the priority
for the 2014 season. However, we are
analyzing that activity could occur at
either Tyonek Deep #1, Tyonek Deep #2,
Southern Cross #1, or Southern Cross #2
to allow for operational flexibility.
Figure 1 in Buccaneer’s IHA application
depicts the location of these four well
sites. All of these wells are located in
State of Alaska oil and gas leases in
Cook Inlet.
Detailed Description of Activities
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1. Drill Rig Mobilization and Towing
Buccaneer proposes to conduct the
exploratory drilling program using the
Endeavour, which is an independent
leg, cantilevered jack-up drill rig of the
Marathon LeTourneau Class 116–C and
is capable of drilling up to 25,000 ft in
water depths from 15–300 ft. Additional
specifications can be found in Appendix
A of the IHA application. The rig will
be towed between drilling locations and
winter moorage by ocean-going tugs
licensed to operate in Cook Inlet. While
under tow, the rig operations will be
monitored by Buccaneer and the drilling
contractor management, both aboard the
rig and onshore.
The jack-up rig would be towed up to
three times during the summer and fall
seasons of 2014. It is estimated that the
longer tows will take 2 days to
complete, while the shorter tows
between the upper Cook Inlet wells will
take but a few hours (distance between
the two wells is less than 5 miles).
The rig will be wet-towed by two or
three ocean-going tugs licensed to
operate in the Cook Inlet. Tugs generate
their loudest sounds while towing due
to propeller cavitation. While these
continuous sounds have been measured
at up to 171 dB re 1 mPa-m (rms) at 1meter source (broadband), they are
generally emitted at dominant
frequencies of less than 5 kHz (Miles et
al., 1987; Richardson et al., 1995,
Simmonds et al., 2004). The distance to
the 120-dB isopleth, assuming a 171 dB
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source, is 1,715 feet (523 meters) using
Collins et al.’s (2007) 171–18.4 Log(R)—
0.00188 R spreading model developed
from Cook Inlet. For the most part, the
dominant noise frequencies from
propeller cavitation are significantly
lower than the dominant hearing
frequencies for pinnipeds and toothed
whales, including beluga whales
(Wartzok and Ketten, 1999).
2. Conductor Pipe Driving
A conductor pipe is a relatively short,
large-diameter pipe driven into the
sediment prior to the drilling of oil
wells. This section of tubing serves to
support the initial sedimentary part of
the well, preventing the looser surface
layer from collapsing and obstructing
the wellbore. The pipe also facilitates
the return of cuttings from the drill
head. Conductor pipes are usually
installed using drilling, pile driving, or
a combination of these techniques. In
offshore wells, the conductor pipe is
also used as a foundation for the
wellhead. Buccaneer proposes to drive
approximately 300 ft (90 m) of 30-inch
conductor pipe at each of the upper
Cook Inlet wells prior to drilling using
a Delmar D62–22 impact hammer. This
hammer has impact weight of 13,640
pounds (6,200 kg) and reaches a
maximum impact energy of 165,215
foot-pounds (224 kilonewton-meters) at
a drop height of 12 feet (3.6 meters).
Blackwell (2005) measured the noise
produced by a Delmar D62–22 driving
36-inch steel pipe in upper Cook Inlet
and found sound pressure levels to
exceed 190 dB re 1mPa-m (rms) at about
200 ft (60 m), 180 dB re 1mPa-m (rms)
at about 820 ft (250 m), and 160 dB re
1mPa-m (rms) at just less than 1.2 mi (1.9
km). Each conductor pipe driving event
is expected to last 1 to 3 days, although
actual sound generation (pounding)
would occur only intermittently during
this period.
3. Exploratory Drilling and Standard
Operation
The jack-up drilling rig Endeavour’s
drilling platform and other noisegenerating equipment is located above
the sea’s surface, and there is very little
surface contact with the water compared
to drill ships and semi-submersible drill
rigs; therefore, lattice-legged jack-up
drill rigs are relatively quiet (Richardson
et al., 1995; Spence et al., 2007).
The Spartan 151, the only other jackup drilling rig operating in the Cook
Inlet, was hydro-acoustically measured
by Marine Acoustics, Inc. (2011) while
operating in 2011. The survey results
showed that continuous noise levels
exceeding 120 dB re 1mPa extended out
only 164 ft (50 m), and that this sound
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was largely associated with the diesel
engines used as hotel power generators.
The Endeavour was hydroacoustically tested during drilling
activities by Illingworth and Rodkin
(2013a) in May 2013 while the rig was
operating at a lower Cook Inlet well site
(Cosmopolitan #1). The results from the
sound source verification indicated that
noise generated from drilling or
generators were below ambient sound
levels. The generators used on the
Endeavour are mounted on pedestals
specifically to reduce noise transfer
through the infrastructure, and they are
enclosed in an insulated engine room,
which may further have reduced
underwater sound transmission to levels
below those generated by the Spartan
151. Also, as mentioned above, the
lattice legs limit transfer of noise
generated from the drilling table to the
water.
The sound source verification
revealed that the submersed deep-well
pumps that charge the fire-suppression
system and cool the generators (in a
closed water system) generate sound
levels exceeding 120 dB re 1mPa out a
distance of approximately 984 ft (300
m). It was not clear at the time of
measurements whether the sound was a
direct result of the pumps or was from
the systems discharge water falling
approximately 40 ft (12 m) from the
deck. Thus, after the falling water was
enclosed in pipe extending below the
water surface in an effort to reduce
sound levels, the pump noise levels
were re-measured in June 2013 (I&R,
2013b) with results indicating that
piping the falling water had a modicum
of effect on reducing underwater sound
levels; nevertheless, the 120-dB radius
still extended out to 853 ft (260 m) in
certain directions. Thus, neither drilling
operations nor running generators on
the Endeavour drill rig generate
underwater sound levels exceeding 120
dB re 1mPa. However, the Endeavour’s
submersed deep-well pumps generate
continuous sound exceeding 120 dB re
1mPa to a maximum distance of 853 ft
(260 m).
4. Vertical Seismic Profiling
Once a well is drilled, accurate
follow-up seismic data can be collected
by placing a receiver at known depths
in the borehole and shooting a seismic
airgun at the surface near the borehole.
This gathered data provides not only
high resolution images of the geological
layers penetrated by the borehole but
can be used to accurately correlate (or
correct) the original surface seismic
data. The procedure is known as VSP.
Buccaneer intends to conduct VSP
operations at the end of drilling each
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well using an array of airguns with total
volumes of between 600 and 880 cubic
inches (in3). Each VSP operation is
expected to last less than 1 or 2 days.
Assuming a 1-meter source level of 227
dB re 1mPa (based on manufacturer’s
specifications) for an 880 in3 array and
using Collins et al.’s (2007) transmission
loss model for Cook Inlet (227—18.4
Log(R)—0.00188), the 190 dB radius
from the source was estimated at 330 ft
(100 m), the 180 dB radius at 1,090 ft
(332 m), and the 160 dB radius at 1.53
mi (2.46 km).
Illingworth and Rodkin (2013c)
measured the underwater sound levels
associated with the July 2013 VSP
operation using a 720 in3 array and
found sound levels exceeding 160 dB re
1 mPa (rms) extended out 1.54 mi (2.47
km), virtually identical to the modeled
distance. The measured radius to 190
dB was 246 ft (75 m) and to 180 dB was
787 ft (240 m). The best fit model for the
empirical data was 227—19.75 log(R)—
0.0 (I&R 2013c).
5. Helicopter and Supply Vessel
Support
Helicopter logistics for project
operations will include transportation
for personnel, groceries, and supplies.
Helicopter support will consist of a twin
turbine Bell 212 (or equivalent)
helicopter certified for instrument flight
rules land and over water operations.
Helicopter crews and support personnel
will be housed in existing Kenai area
facilities. The helicopter will be based at
the Kenai Airport to support rig crew
changes and cargo handling. Fueling
will take place at these facilities. No
helicopter refueling will take place on
the rig.
Helicopter flights to and from the rig
are expected to average two per day.
Flight routes will follow a direct route
to and from the rig location, and flight
heights will be maintained 1,000 to
1,500 feet above ground level to avoid
take of marine mammals (Richardson et
al., 1995). At these altitudes, there are
not expected to be impacts from sound
generation on marine mammals. The
aircraft will be dedicated to the drilling
operation and will be available for
service 24 hours per day. A replacement
aircraft will be available when major
maintenance items are scheduled.
Major supplies will be staged onshore at the Kenai OSK Dock. Required
supplies and equipment will be moved
from the staging area by contracted
supply vessels and loaded aboard the rig
when the rig is established on a drilling
location. Major supplies will include
fuel, drilling water, mud materials,
cement, casing, and well service
equipment. Supply vessels also will be
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outfitted with fire-fighting systems as
part of fire prevention and control as
required by Cook Inlet Spill Prevention
and Response, Inc. The specific supply
vessels have not been identified;
however, typical offshore drilling
support work vessels are of steel
construction with strengthened hulls to
give the capability of working in
extreme conditions. Additional
information about logistics and fuel and
waste management can be found in
Section 1.2 of Buccaneer’s IHA
application.
Description of Marine Mammals in the
Area of the Specified Activity
The marine mammal species under
NMFS’s jurisdiction that could occur
near the exploratory drilling sites in
upper Cook Inlet include two cetacean
species, both odontocetes (toothed
whales): beluga whale (Delphinapterus
leucas) and harbor porpoise (Phocoena
phocoena) and one pinniped species:
harbor seal (Phoca vitulina richardsi).
The marine mammal species that is
likely to be encountered most widely (in
space and time) throughout the period
of the planned surveys is the harbor
seal. While killer whales (Orcinus orca)
and Steller sea lions (Eumetopias
jubatus) have been sighted in upper
Cook Inlet, their occurrence is
considered rare in that portion of the
Inlet. There have also been a few
sightings in the last couple of years of
gray whales (Eschrichtius robustus) in
the upper inlet; however occurrence is
rare. Gray whales, killer whales, Steller
sea lions, minke whales (Balaenoptera
acutorostrata), and Dall’s porpoises
(Phocoenoides dalli) are more likely to
occur in lower Cook Inlet (where rig
towing would occur).
Of these marine mammal species,
Cook Inlet beluga whales and the
western distinct population segment
(DPS) of Steller sea lions are listed as
endangered under the Endangered
Species Act (ESA). The eastern DPS was
recently removed from the endangered
species list (78 FR 66139, November 4,
2013) but currently retains its status as
‘‘depleted’’ under the MMPA along with
the western DPS and Cook Inlet beluga
whales.
Despite these designations, Cook Inlet
beluga whales and the western DPS of
Steller sea lions have not made
significant progress towards recovery.
Data indicate that the Cook Inlet
population of beluga whales has been
decreasing at a rate of 1.1 percent
annually between 2001 and 2011 (Allen
and Angliss, 2013). A recent review of
the status of the population indicated
that there is an 80% chance that the
population will decline further (Hobbs
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and Shelden 2008). Counts of non-pup
Steller sea lions at trend sites in the
Alaska western stock increased 11%
from 2000 to 2004 (Allen and Angliss,
2013). These were the first region-wide
increases for the western stock since
standardized surveys began in the 1970s
and were due to increased or stable
counts in all regions except the western
Aleutian Islands. Between 2004 and
2008, Alaska western non-pup counts
increased only 3%: eastern Gulf of
Alaska (Prince William Sound area)
counts were higher and Kenai Peninsula
through Kiska Island counts were stable,
but western Aleutian counts continued
to decline. Johnson (2010) analyzed
western Steller sea lion population
trends in Alaska and concluded that the
overall 2000–2008 trend was a decline
1.5% per year; however, there continues
to be considerable regional variability in
recent trends (Allen and Angliss, 2013).
NMFS has not been able to complete a
non-pup survey of the AK western stock
since 2008, due largely to weather and
closure of the Air Force base on Shemya
in 2009 and 2010.
Pursuant to the ESA, critical habitat
has been designated for Cook Inlet
beluga whales and Steller sea lions. The
proposed action falls within critical
habitat designated in Cook Inlet for
beluga whales but is not within critical
habitat designated for Steller sea lions.
Buccaneer’s Southern Cross and Tyonek
Deep well sites occur in areas identified
as Area 2 in the critical habitat
designation. The wells are located south
of the Area 1 critical habitat designation
where belugas are particularly
vulnerable to impacts due to their high
seasonal densities and the biological
importance of the area for foraging,
nursery, and predator avoidance. Area 2
is based on dispersed fall and winter
feeding and transit areas in waters
where whales typically appear in
smaller densities or deeper waters (76
FR 20180, April 11, 2011).
Buccaneer did not request take of
beluga whales or Steller sea lions.
Informal consultation pursuant to
section 7 of the ESA was conducted for
this project, and it was determined that
the activity is not likely to adversely
affect listed species or critical habitat
based upon the nature of the activities
and specific mitigation measures to
ensure that take of these species or
adverse habitat impacts are unlikely.
This is discussed further in the
‘‘Proposed Mitigation’’ section later in
this document.
Other species of mysticetes that have
been observed infrequently in lower
Cook Inlet include: humpback whale
(Megaptera novaeangliae) and fin whale
(Balaenoptera physalus). Because of
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their infrequent occurrence Cook Inlet,
they are not included in this proposed
IHA notice. Sea otters also occur in
Cook Inlet. However, sea otters are
managed by the U.S. Fish and Wildlife
Service and are therefore not considered
further in this proposed IHA notice.
Information summaries for the species
for which take is requested is provided
next.
Cetaceans
1. Killer Whales
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In general, killer whales are rare in
upper Cook Inlet, where transient killer
whales are known to feed on beluga
whales, and resident killer whales are
known to feed on anadromous fish
(Shelden et al., 2003). The availability
of these prey species largely determines
the likeliest times for killer whales to be
in the area. Between 1993 and 2004, 23
sightings of killer whales were reported
in the lower Cook Inlet during aerial
surveys by Rugh et al. (2005). Surveys
conducted over a span of 20 years by
Shelden et al. (2003) reported 11
sightings in upper Cook Inlet between
Turnagain Arm, Susitna Flats, and Knik
Arm. No killer whales were spotted
during recent surveys by Funk et al.
(2005), Ireland et al. (2005), Brueggeman
et al. (2007a, 2007b, 2008), or Prevel
Ramos et al. (2006, 2008). Eleven killer
whale strandings have been reported in
Turnagain Arm, six in May 1991 and
five in August 1993. Therefore, very few
killer whales, if any, are expected to
approach or be in the vicinity of the
action area.
2. Harbor Porpoise
The most recent estimated density for
harbor porpoises in Cook Inlet is 7.2 per
1,000 km2 (Dahlheim et al., 2000)
indicating that only a small number use
Cook Inlet. Harbor porpoise have been
reported in lower Cook Inlet from Cape
Douglas to the West Foreland,
Kachemak Bay, and offshore (Rugh et
al., 2005). Small numbers of harbor
porpoises have been consistently
reported in upper Cook Inlet between
April and October, except for a recent
survey that recorded higher than usual
numbers (Prevel Ramos et al., 2008).
Prevel Ramos et al. (2008) reported 17
harbor porpoises from spring to fall
2006, while other studies reported 14 in
the spring of 2007 (Brueggeman et al.
2007) and 12 in the fall of 2007
(Brueggeman et al. 2008). During the
spring and fall of 2007, 129 harbor
porpoises were reported between
Granite Point and the Susitna River;
however, the reason for the increase in
numbers of harbor porpoise in the upper
Cook Inlet remains unclear and the
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disparity with the result of past
sightings suggests that it may be an
anomaly. The spike in reported
sightings occurred in July, which was
followed by sightings of 79 harbor
porpoises in August, 78 in September,
and 59 in October 2007. It is important
to note that the number of porpoises
counted more than once was unknown,
which suggests that the actual numbers
are likely smaller than those reported. In
addition, recent passive acoustic
research in Cook Inlet by the Alaska
Department of Fish and Game and the
National Marine Mammal Laboratory
have indicated that harbor porpoises
occur in the area more frequently than
previously thought, particularly in the
West Foreland area in the spring (NMFS
2011); however overall numbers are still
unknown at this time.
3. Gray Whale
The gray whale is a large baleen
whale known to have one of the longest
migrations of any mammal. This whale
can be found all along the shallow
coastal waters of the North Pacific
Ocean.
The Eastern North Pacific stock,
which includes those whales that travel
along the coast of Alaska, was delisted
from the ESA in 1994 after a distinction
was made between the western and
eastern populations (59 FR 31094, June
16, 1994). It is estimated that
approximately 18,000 individuals exist
in the eastern stock (Allen and Angliss,
2012).
Although observations of gray whales
are rare within Cook Inlet, marine
mammal observers noted individual
gray whales on nine occasions in upper
Cook Inlet in 2012 while conducting
marine mammal monitoring for seismic
survey activities under an IHA NMFS
issued to Apache Alaska Corporation:
four times in May; twice in June; and
three times in July (Apache, 2013).
Annual surveys conducted by NMFS in
Cook Inlet since 1993 have resulted in
a total of five gray whale sightings (Rugh
et al., 2005). Although Cook Inlet is not
believed to comprise either essential
feeding or social ground, and gray
whales are typically not observed
within upper Cook Inlet, there may be
some encounters in lower Cook Inlet
during towing activities and perhaps an
incidental encounter in the upper Inlet.
4. Minke Whale
Minke whales are the smallest of the
rorqual group of baleen whales. There
are no population estimates for the
North Pacific, although estimates have
been made for some portions of Alaska.
Zerbini et al. (2006) estimated the
coastal population between Kenai
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Fjords and the Aleutian Islands at 1,233
animals. During Cook Inlet-wide aerial
surveys conducted from 1993 to 2004,
minke whales were encountered only
twice (1998, 1999), both times off
Anchor Point 16 mi northwest of
Homer. A minke whale was also
reported off Cape Starichkof in 2011 (A.
Holmes, pers. comm.) and 2013 (E.
Fernandez and C. Hesselbach, pers.
comm.), suggesting this location is
regularly used by minke whales,
including during the winter. There are
no records north of Cape Starichkof, and
this species is unlikely to be seen in
upper Cook Inlet. There is a chance of
encountering this whale during towing
operations through lower Cook Inlet.
5. Dall’s Porpoise
Dall’s porpoise are widely distributed
throughout the North Pacific Ocean
including Alaska, although they are not
found in upper Cook Inlet and the
shallower waters of the Bering, Chukchi,
and Beaufort Seas (Allen and Angliss,
2013). The Alaskan population has been
estimated at 83,400 animals (Allen and
Angliss, 2013), making it one of the
more common cetaceans in the state.
Dall’s porpoise have been observed in
lower Cook Inlet, including Kachemak
Bay and near Anchor Point (Glenn
Johnson, pers. comm.), but sightings
there are rare. There is only the remote
chance that Dall’s porpoise might be
observed during Buccaneer towing
operations through lower Cook Inlet.
Pinnipeds
1. Harbor Seals
Harbor seals inhabit the coastal and
estuarine waters of Cook Inlet and are
one of the more common marine
mammal species in Alaskan waters.
Harbor seals are non-migratory; their
movements are associated with tides,
weather, season, food availability, and
reproduction. The major haulout sites
for harbor seals are located in lower
Cook Inlet, and their presence in the
upper inlet coincides with seasonal runs
of prey species. For example, harbor
seals are commonly observed along the
Susitna River and other tributaries along
upper Cook Inlet during the eulachon
and salmon migrations (NMFS, 2003).
During aerial surveys of upper Cook
Inlet in 2001, 2002, and 2003, harbor
seals were observed 24 to 96 km (15 to
60 mi) south-southwest of Anchorage at
the Chickaloon, Little Susitna, Susitna,
Ivan, McArthur, and Beluga Rivers
(Rugh et al., 2005). Montgomery et al.
(2007) recorded over 200 haulout sites
in lower Cook Inlet alone. However,
only a few dozen to a couple hundred
seals seasonally occur in upper Cook
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Inlet (Rugh et al., 2005), mostly at the
mouth of the Susitna River where their
numbers vary in concert with the spring
eulachon and summer salmon runs
(Nemeth et al., 2007, Boveng et al.,
2012). Montgomery et al. (2007) also
found seals elsewhere in Cook Inlet to
move in response to local steelhead and
salmon runs. However, aerial surveys
conducted in June 2013 for the
proposed Susitna Dam project noted
nearly 700 harbor seals in the Susitna
Delta region (Alaska Energy Authority,
2013). Harbor seals may be encountered
during rig tows to and from Cape
Starichkof, and possibly during drilling
in upper Cook Inlet.
As mentioned previously, take of
marine mammals listed under the ESA
will not occur because of mitigation
measures to ensure no take of those
species. Buccaneer’s application
contains information on the status,
distribution, seasonal distribution, and
abundance of each of the species under
NMFS jurisdiction mentioned in this
document. Please refer to the
application for that information (see
ADDRESSES). Additional information can
also be found in the NMFS Stock
Assessment Reports (SAR). The Alaska
2012 SAR is available on the Internet at:
https://www.nmfs.noaa.gov/pr/sars/pdf/
ak2012.pdf.
Potential Effects of the Specified
Activity on Marine Mammals
This section includes a summary and
discussion of the ways that the types of
stressors associated with the specified
activity (e.g., driving of the conductor
pipe; exploratory drilling; towing of the
jack-up drill rig; and VSP) have been
observed to or are thought to impact
marine mammals. This section may
include a discussion of known effects
that do not rise to the level of an MMPA
take (for example, with acoustics, we
may include a discussion of studies that
showed animals not reacting at all to
sound or exhibiting barely measurable
avoidance). The discussion may also
include reactions that we consider to
rise to the level of a take and those that
we do not consider to rise to the level
of a take. This section is intended as a
background of potential effects and does
not consider either the specific manner
in which this activity will be carried out
or the mitigation that will be
implemented or how either of those will
shape the anticipated impacts from this
specific activity. The ‘‘Estimated Take
by Incidental Harassment’’ section later
in this document will include a
quantitative analysis of the number of
individuals that are expected to be taken
by this activity. The ‘‘Negligible Impact
Analysis’’ section will include the
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analysis of how this specific activity
will impact marine mammals and will
consider the content of this section, the
‘‘Estimated Take by Incidental
Harassment’’ section, the ‘‘Mitigation’’
section, and the ‘‘Anticipated Effects on
Marine Mammal Habitat’’ section to
draw conclusions regarding the likely
impacts of this activity on the
reproductive success or survivorship of
individuals and from that on the
affected marine mammal populations or
stocks.
The likely or possible impacts of the
proposed drilling program in upper
Cook Inlet on marine mammals could
involve both non-acoustic and acoustic
stressors. Potential non-acoustic
stressors could result from the physical
presence of the equipment and
personnel. Petroleum development and
associated activities introduce sound
into the marine environment. Impacts to
marine mammals are expected to
primarily be acoustic in nature.
Potential acoustic effects on marine
mammals relate to sound produced by
drilling activity, conductor pipe driving,
and rig towing, as well as the VSP
airgun array.
Acoustic Impacts
When considering the influence of
various kinds of sound on the marine
environment, it is necessary to
understand that different kinds of
marine life are sensitive to different
frequencies of sound. Based on available
behavioral data, audiograms have been
derived using auditory evoked
potentials, anatomical modeling, and
other data, Southall et al. (2007)
designate ‘‘functional hearing groups’’
for marine mammals and estimate the
lower and upper frequencies of
functional hearing of the groups. The
functional groups and the associated
frequencies are indicated below (though
animals are less sensitive to sounds at
the outer edge of their functional range
and most sensitive to sounds of
frequencies within a smaller range
somewhere in the middle of their
functional hearing range):
• Low frequency cetaceans (13
species of mysticetes): Functional
hearing is estimated to occur between
approximately 7 Hz and 30 kHz;
• Mid-frequency cetaceans (32
species of dolphins, six species of larger
toothed whales, and 19 species of
beaked and bottlenose whales):
Functional hearing is estimated to occur
between approximately 150 Hz and 160
kHz;
• High frequency cetaceans (eight
species of true porpoises, six species of
river dolphins, Kogia, the franciscana,
and four species of cephalorhynchids):
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Functional hearing is estimated to occur
between approximately 200 Hz and 180
kHz;
• Phocid pinnipeds in Water:
Functional hearing is estimated to occur
between approximately 75 Hz and 100
kHz; and
• Otariid pinnipeds in Water:
Functional hearing is estimated to occur
between approximately 100 Hz and 40
kHz.
As mentioned previously in this
document, six marine mammal species
(five cetacean and one phocid pinniped)
may occur in the exploratory drilling
area or in the rig tow area. Of the five
cetacean species likely to occur in the
proposed project area and for which
take is requested, two are classified as
low-frequency cetaceans (i.e., minke
and gray whales), one is classified as a
mid-frequency cetacean (i.e., killer
whale), and two are classified as a highfrequency cetaceans (i.e., harbor and
Dall’s porpoises) (Southall et al., 2007).
A species’ functional hearing group is a
consideration when we analyze the
effects of exposure to sound on marine
mammals.
1. Tolerance
Numerous studies have shown that
underwater sounds from industry
activities are often readily detectable by
marine mammals in the water at
distances of many kilometers.
Numerous studies have also shown that
marine mammals at distances more than
a few kilometers away often show no
apparent response to industry activities
of various types (Miller et al., 2005; Bain
and Williams, 2006). This is often true
even in cases when the sounds must be
readily audible to the animals based on
measured received levels and the
hearing sensitivity of that mammal
group. Although various baleen whales,
toothed whales, and (less frequently)
pinnipeds have been shown to react
behaviorally to underwater sound such
as airgun pulses or vessels under some
conditions, at other times mammals of
all three types have shown no overt
reactions (e.g., Malme et al., 1986;
Richardson et al., 1995; Madsen and
Mohl, 2000; Croll et al., 2001; Jacobs
and Terhune, 2002; Madsen et al., 2002;
Miller et al., 2005). Weir (2008)
observed marine mammal responses to
seismic pulses from a 24 airgun array
firing a total volume of either 5,085 in3
or 3,147 in3 in Angolan waters between
August 2004 and May 2005. Weir
recorded a total of 207 sightings of
humpback whales (n = 66), sperm
whales (n = 124), and Atlantic spotted
dolphins (n = 17) and reported that
there were no significant differences in
encounter rates (sightings/hr) for
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humpback and sperm whales according
to the airgun array’s operational status
(i.e., active versus silent). The airgun
arrays used in the Weir (2008) study
were much larger than the array
proposed for use during the limited VSP
(total discharge volumes of 600 to 880
in3 for 1 to 2 days per well). In general,
pinnipeds and small odontocetes seem
to be more tolerant of exposure to some
types of underwater sound than are
baleen whales. Richardson et al. (1995b)
found that vessel noise does not seem to
strongly affect pinnipeds that are
already in the water. Richardson et al.
(1995b) went on to explain that seals on
haul-outs sometimes respond strongly to
the presence of vessels and at other
times appear to show considerable
tolerance of vessels.
2. Masking
Masking is the obscuring of sounds of
interest by other sounds, often at similar
frequencies. Marine mammals use
acoustic signals for a variety of
purposes, which differ among species,
but include communication between
individuals, navigation, foraging,
reproduction, avoiding predators, and
learning about their environment (Erbe
and Farmer, 2000; Tyack, 2000).
Masking, or auditory interference,
generally occurs when sounds in the
environment are louder than, and of a
similar frequency as, auditory signals an
animal is trying to receive. Masking is
a phenomenon that affects animals that
are trying to receive acoustic
information about their environment,
including sounds from other members
of their species, predators, prey, and
sounds that allow them to orient in their
environment. Masking these acoustic
signals can disturb the behavior of
individual animals, groups of animals,
or entire populations.
Masking occurs when anthropogenic
sounds and signals (that the animal
utilizes) overlap at both spectral and
temporal scales. The sounds generated
by the proposed equipment for the
exploratory drilling program will
consist of low frequency sources (most
under 500 Hz). Lower frequency manmade sounds are more likely to affect
detection of communication calls and
other potentially important natural
sounds such as surf and prey noise.
There is little concern regarding
masking near the jack-up rig during
exploratory drilling operations, as the
species most likely to be found in the
vicinity are mid- to high-frequency
cetaceans or pinnipeds and not lowfrequency cetaceans. Additionally,
masking is not expected to be a concern
from airgun usage due to the brief
duration of use (less than a day to up
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to 2 days per well) and the lowfrequency sounds that are produced by
the airguns. However, at long distances
(over tens of kilometers away), due to
multipath propagation and
reverberation, the durations of airgun
pulses can be ‘‘stretched’’ to seconds
with long decays (Madsen et al., 2006),
although the intensity of the sound is
greatly reduced.
This could affect communication
signals used by low frequency
mysticetes when they occur near the
noise band and thus reduce the
communication space of animals (e.g.,
Clark et al., 2009) and cause increased
stress levels (e.g., Foote et al., 2004; Holt
et al., 2009); however, no baleen whales
are expected to occur within the
proposed action area in the upper Inlet.
A few may be encountered in the lower
Inlet during the rig towing. Marine
mammals are thought to sometimes be
able to compensate for masking by
adjusting their acoustic behavior by
shifting call frequencies, and/or
increasing call volume and vocalization
rates. For example, blue whales are
found to increase call rates when
exposed to seismic survey noise in the
St. Lawrence Estuary (Di Iorio and
Clark, 2010). The North Atlantic right
whales (Eubalaena glacialis) exposed to
high shipping noise increase call
frequency (Parks et al., 2007), while
some humpback whales respond to lowfrequency active sonar playbacks by
increasing song length (Miller el al.,
2000). Additionally, beluga whales have
been known to change their
vocalizations in the presence of high
background noise possibly to avoid
masking calls (Au et al., 1985; Lesage et
al., 1999; Scheifele et al., 2005).
Although some degree of masking is
inevitable when high levels of manmade
broadband sounds are introduced into
the sea, marine mammals have evolved
systems and behavior that function to
reduce the impacts of masking.
Structured signals, such as the
echolocation click sequences of small
toothed whales, may be readily detected
even in the presence of strong
background noise because their
frequency content and temporal features
usually differ strongly from those of the
background noise (Au and Moore, 1988,
1990). The components of background
noise that are similar in frequency to the
sound signal in question primarily
determine the degree of masking of that
signal.
Redundancy and context can also
facilitate detection of weak signals.
These phenomena may help marine
mammals detect weak sounds in the
presence of natural or manmade noise.
Most masking studies in marine
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19257
mammals present the test signal and the
masking noise from the same direction.
The sound localization abilities of
marine mammals suggest that, if signal
and noise come from different
directions, masking would not be as
severe as the usual types of masking
studies might suggest (Richardson et al.,
1995). The dominant background noise
may be highly directional if it comes
from a particular anthropogenic source
such as a ship or industrial site.
Directional hearing may significantly
reduce the masking effects of these
sounds by improving the effective
signal-to-noise ratio. In the cases of
higher frequency hearing by the
bottlenose dolphin, beluga whale, and
killer whale, empirical evidence
confirms that masking depends strongly
on the relative directions of arrival of
sound signals and the masking noise
(Penner et al., 1986; Dubrovskiy, 1990;
Bain et al., 1993; Bain and Dahlheim,
1994). Toothed whales, and probably
other marine mammals as well, have
additional capabilities besides
directional hearing that can facilitate
detection of sounds in the presence of
background noise. There is evidence
that some toothed whales can shift the
dominant frequencies of their
echolocation signals from a frequency
range with a lot of ambient noise toward
frequencies with less noise (Au et al.,
1974, 1985; Moore and Pawloski, 1990;
Thomas and Turl, 1990; Romanenko
and Kitain, 1992; Lesage et al., 1999). A
few marine mammal species are known
to increase the source levels or alter the
frequency of their calls in the presence
of elevated sound levels (Dahlheim,
1987; Au, 1993; Lesage et al., 1993,
1999; Terhune, 1999; Foote et al., 2004;
Parks et al., 2007, 2009; Di Iorio and
Clark, 2009; Holt et al., 2009).
These data demonstrating adaptations
for reduced masking pertain mainly to
the very high frequency echolocation
signals of toothed whales. There is less
information about the existence of
corresponding mechanisms at moderate
or low frequencies or in other types of
marine mammals. For example, Zaitseva
et al. (1980) found that, for the
bottlenose dolphin, the angular
separation between a sound source and
a masking noise source had little effect
on the degree of masking when the
sound frequency was 18 kHz, in contrast
to the pronounced effect at higher
frequencies. Directional hearing has
been demonstrated at frequencies as low
as 0.5–2 kHz in several marine
mammals, including killer whales
(Richardson et al., 1995a). This ability
may be useful in reducing masking at
these frequencies. In summary, high
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levels of sound generated by
anthropogenic activities may act to
mask the detection of weaker
biologically important sounds by some
marine mammals. This masking may be
more prominent for lower frequencies.
For higher frequencies, such as that
used in echolocation by toothed whales,
several mechanisms are available that
may allow them to reduce the effects of
such masking.
3. Behavioral Disturbance
Behavioral responses to sound are
highly variable and context-specific.
Many different variables can influence
an animal’s perception of and response
to (in both nature and magnitude) an
acoustic event. An animal’s prior
experience with a sound or sound
source affects whether it is less likely
(habituation) or more likely
(sensitization) to respond to certain
sounds in the future (animals can also
be innately pre-disposed to respond to
certain sounds in certain ways; Southall
et al., 2007). Related to the sound itself,
the perceived nearness of the sound,
bearing of the sound (approaching vs.
retreating), similarity of a sound to
biologically relevant sounds in the
animal’s environment (i.e., calls of
predators, prey, or conspecifics), and
familiarity of the sound may affect the
way an animal responds to the sound
(Southall et al., 2007). Individuals (of
different age, gender, reproductive
status, etc.) among most populations
will have variable hearing capabilities
and differing behavioral sensitivities to
sounds that will be affected by prior
conditioning, experience, and current
activities of those individuals. Often,
specific acoustic features of the sound
and contextual variables (i.e., proximity,
duration, or recurrence of the sound or
the current behavior that the marine
mammal is engaged in or its prior
experience), as well as entirely separate
factors such as the physical presence of
a nearby vessel, may be more relevant
to the animal’s response than the
received level alone.
Exposure of marine mammals to
sound sources can result in (but is not
limited to) no response or any of the
following observable responses:
Increased alertness; orientation or
attraction to a sound source; vocal
modifications; cessation of feeding;
cessation of social interaction; alteration
of movement or diving behavior;
avoidance; habitat abandonment
(temporary or permanent); and, in
severe cases, panic, flight, stampede, or
stranding, potentially resulting in death
(Southall et al., 2007). The biological
significance of many of these behavioral
disturbances is difficult to predict,
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especially if the detected disturbances
appear minor. However, the
consequences of behavioral
modification have the potential to be
biologically significant if the change
affects growth, survival, or
reproduction. Examples of significant
behavioral modifications include:
• Drastic change in diving/surfacing
patterns (such as those thought to be
causing beaked whale stranding due to
exposure to military mid-frequency
tactical sonar);
• Habitat abandonment due to loss of
desirable acoustic environment; and
• Cessation of feeding or social
interaction.
Detailed studies regarding responses
to anthropogenic sound have been
conducted on humpback, gray, and
bowhead whales and ringed seals. Less
detailed data are available for some
other species of baleen whales, sperm
whales, small toothed whales, and sea
otters. The following sub-sections
provide examples of behavioral
responses that provide an idea of the
variability in behavioral responses that
would be expected given the different
sensitivities of marine mammal species
to sound. However, baleen whales are
unlikely to occur in the vicinity of the
well sites and are only somewhat likely
to occur in the lower portions of Cook
Inlet during rig towing activities.
Baleen Whales—Richardson et al.
(1995a) reported changes in surfacing
and respiration behavior and the
occurrence of turns during surfacing in
bowhead whales exposed to playback of
underwater sound from drilling
activities. These behavioral effects were
localized and occurred at distances up
to 1.2–2.5 mi (2–4 km).
Richardson et al. (2008) reported a
slight change in the distribution of
bowhead whale calls in response to
operational sounds on BP’s Northstar
Island. The southern edge of the call
distribution ranged from 0.47 to 1.46 mi
(0.76 to 2.35 km) farther offshore,
apparently in response to industrial
sound levels. This result however, was
only achieved after intensive statistical
analyses, and it is not clear that this
represented a biologically significant
effect.
Richardson et al. (1995a) and Moore
and Clarke (2002) reviewed a few
studies that observed responses of gray
whales to aircraft. Cow-calf pairs were
quite sensitive to a turboprop survey
flown at 1,000 ft (305 m) altitude on the
Alaskan summering grounds. In that
survey, adults were seen swimming over
the calf, or the calf swam under the
adult (Ljungblad et al., 1983, cited in
Richardson et al., 1995b and Moore and
Clarke, 2002). However, when the same
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aircraft circled for more than 10 minutes
at 1,050 ft (320 m) altitude over a group
of mating gray whales, no reactions
were observed (Ljungblad et al., 1987,
cited in Moore and Clarke, 2002).
Malme et al. (1984, cited in Richardson
et al., 1995b and Moore and Clarke,
2002) conducted playback experiments
on migrating gray whales. They exposed
the animals to underwater noise
recorded from a Bell 212 helicopter
(estimated altitude=328 ft [100 m]), at
an average of three simulated passes per
minute. The authors observed that
whales changed their swimming course
and sometimes slowed down in
response to the playback sound but
proceeded to migrate past the
transducer. Migrating gray whales did
not react overtly to a Bell 212 helicopter
at greater than 1,394 ft (425 m) altitude,
occasionally reacted when the
helicopter was at 1,000–1,198 ft (305–
365 m), and usually reacted when it was
below 825 ft (250 m; Southwest
Research Associates, 1988, cited in
Richardson et al., 1995b and Moore and
Clarke, 2002). Reactions noted in that
study included abrupt turns or dives or
both. Green et al. (1992, cited in
Richardson et al., 1995b) observed that
migrating gray whales rarely exhibited
noticeable reactions to a straight-line
overflight by a Twin Otter at 197 ft (60
m) altitude. Restrictions on aircraft
altitude will be part of the proposed
mitigation measures (described in the
‘‘Proposed Mitigation’’ section later in
this document) during the proposed
drilling activities, and overflights are
likely to have little or no disturbance
effects on baleen whales. Any
disturbance that may occur would likely
be temporary and localized.
Southall et al. (2007, Appendix C)
reviewed a number of papers describing
the responses of marine mammals to
non-pulsed sound, such as that
produced during exploratory drilling
operations. In general, little or no
response was observed in animals
exposed at received levels from 90–120
dB re 1 mPa (rms). Probability of
avoidance and other behavioral effects
increased when received levels were
from 120–160 dB re 1 mPa (rms). Some
of the relevant reviews contained in
Southall et al. (2007) are summarized
next.
Baker et al. (1982) reported some
avoidance by humpback whales to
vessel noise when received levels were
110–120 dB (rms) and clear avoidance at
120–140 dB (sound measurements were
not provided by Baker but were based
on measurements of identical vessels by
Miles and Malme, 1983).
Malme et al. (1983, 1984) used
playbacks of sounds from helicopter
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overflight and drilling rigs and
platforms to study behavioral effects on
migrating gray whales. Received levels
exceeding 120 dB induced avoidance
reactions. Malme et al. (1984) calculated
10%, 50%, and 90% probabilities of
gray whale avoidance reactions at
received levels of 110, 120, and 130 dB,
respectively. Malme et al. (1986)
observed the behavior of feeding gray
whales during four experimental
playbacks of drilling sounds (50 to 315
Hz; 21- min overall duration and 10%
duty cycle; source levels of 156–162
dB). In two cases for received levels of
100–110 dB, no behavioral reaction was
observed. However, avoidance behavior
was observed in two cases where
received levels were 110–120 dB.
Richardson et al. (1990) performed 12
playback experiments in which
bowhead whales in the Alaskan Arctic
were exposed to drilling sounds. Whales
generally did not respond to exposures
in the 100 to 130 dB range, although
there was some indication of minor
behavioral changes in several instances.
McCauley et al. (1996) reported
several cases of humpback whales
responding to vessels in Hervey Bay,
Australia. Results indicated clear
avoidance at received levels between
118 to 124 dB in three cases for which
response and received levels were
observed/measured.
Palka and Hammond (2001) analyzed
line transect census data in which the
orientation and distance off transect line
were reported for large numbers of
minke whales. The authors developed a
method to account for effects of animal
movement in response to sighting
platforms. Minor changes in locomotion
speed, direction, and/or diving profile
were reported at ranges from 1,847 to
2,352 ft (563 to 717 m) at received levels
of 110 to 120 dB.
Biassoni et al. (2000) and Miller et al.
(2000) reported behavioral observations
for humpback whales exposed to a lowfrequency sonar stimulus (160- to 330Hz frequency band; 42-s tonal signal
repeated every 6 min; source levels 170
to 200 dB) during playback experiments.
Exposure to measured received levels
ranging from 120 to 150 dB resulted in
variability in humpback singing
behavior. Croll et al. (2001) investigated
responses of foraging fin and blue
whales to the same low frequency active
sonar stimulus off southern California.
Playbacks and control intervals with no
transmission were used to investigate
behavior and distribution on time scales
of several weeks and spatial scales of
tens of kilometers. The general
conclusion was that whales remained
feeding within a region for which 12 to
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30 percent of exposures exceeded 140
dB.
Frankel and Clark (1998) conducted
playback experiments with wintering
humpback whales using a single speaker
producing a low-frequency ‘‘Msequence’’ (sine wave with multiplephase reversals) signal in the 60 to 90
Hz band with output of 172 dB at 1 m.
For 11 playbacks, exposures were
between 120 and 130 dB re 1 mPa (rms)
and included sufficient information
regarding individual responses. During
eight of the trials, there were no
measurable differences in tracks or
bearings relative to control conditions,
whereas on three occasions, whales
either moved slightly away from (n=1)
or towards (n=2) the playback speaker
during exposure. The presence of the
source vessel itself had a greater effect
than did the M-sequence playback.
Finally, Nowacek et al. (2004) used
controlled exposures to demonstrate
behavioral reactions of northern right
whales to various non-pulse sounds.
Playback stimuli included ship noise,
social sounds of conspecifics, and a
complex, 18-min ‘‘alert’’ sound
consisting of repetitions of three
different artificial signals. Ten whales
were tagged with calibrated instruments
that measured received sound
characteristics and concurrent animal
movements in three dimensions. Five
out of six exposed whales reacted
strongly to alert signals at measured
received levels between 130 and 150 dB
(i.e., ceased foraging and swam rapidly
to the surface). Two of these individuals
were not exposed to ship noise, and the
other four were exposed to both stimuli.
These whales reacted mildly to
conspecific signals. Seven whales,
including the four exposed to the alert
stimulus, had no measurable response
to either ship sounds or actual vessel
noise.
Baleen whale responses to pulsed
sound (e.g., seismic airguns) have been
studied more thoroughly than responses
to continuous sound (e.g., drill rigs).
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
greater distances (Miller et al., 2005).
However, baleen whales exposed to
strong noise pulses often react by
deviating from their normal migration
route (Richardson et al., 1999).
Migrating gray and bowhead whales
were observed avoiding the sound
source by displacing their migration
route to varying degrees but within the
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natural boundaries of the migration
corridors (Schick and Urban, 2000;
Richardson et al., 1999; Malme et al.,
1983). Baleen whale responses to pulsed
sound however may depend on the type
of activity in which the whales are
engaged. Some evidence suggests that
feeding bowhead whales may be more
tolerant of underwater sound than
migrating bowheads (Miller et al., 2005;
Lyons et al., 2009; Christie et al., 2010).
Results of studies of gray, bowhead,
and humpback whales have determined
that received levels of pulses in the
160–170 dB re 1 mPa 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
2.8–9 mi (4.5–14.5 km) from the source.
For the much smaller airgun array used
during the VSP survey (total discharge
volume between 600 and 880 in3), the
distance to a received level of 160 dB re
1 mPa rms is estimated to be 1.53 mi
(2.47 km). 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
have shown that some species of baleen
whales, notably bowhead and
humpback whales, at times show strong
avoidance at received levels lower than
160–170 dB re 1 mPa rms.
Malme et al. (1986, 1988) studied the
responses of feeding eastern gray whales
to pulses from a single 100 in3 airgun off
St. Lawrence Island in the northern
Bering Sea. They estimated, based on
small sample sizes, that 50% of feeding
gray whales ceased feeding at an average
received pressure level of 173 dB re 1
m Pa on an (approximate) rms basis, and
that 10% 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 the distribution of
feeding Western Pacific gray whales off
Sakhalin Island, Russia, during a
seismic survey (Yazvenko et al., 2007).
Data on short-term reactions (or lack
of reactions) of cetaceans to impulsive
noises do not necessarily provide
information about long-term effects.
While it is not certain whether
impulsive noises affect reproductive
rate or distribution and habitat use in
subsequent days or years, certain
species have continued to use areas
ensonified by airguns and have
continued to increase in number despite
successive years of anthropogenic
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activity in the area. 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). In any event, the brief exposures
to sound pulses from the proposed
airgun source (the airguns will only be
fired for a few hours at a time over the
course of 1 to 2 days per well) are highly
unlikely to result in prolonged effects.
Toothed Whales—Most toothed
whales have the greatest hearing
sensitivity at frequencies much higher
than that of baleen whales and may be
less responsive to low-frequency sound
commonly associated with oil and gas
industry exploratory drilling activities.
Richardson et al. (1995a) reported that
beluga whales did not show any
apparent reaction to playback of
underwater drilling sounds at distances
greater than 656–1,312 ft (200–400 m).
Reactions included slowing down,
milling, or reversal of course after which
the whales continued past the projector,
sometimes within 164–328 ft (50–100
m). The authors concluded (based on a
small sample size) that the playback of
drilling sounds had no biologically
significant effects on migration routes of
beluga whales migrating through pack
ice and along the seaward side of the
nearshore lead east of Point Barrow in
spring.
At least six of 17 groups of beluga
whales appeared to alter their migration
path in response to underwater
playbacks of icebreaker sound
(Richardson et al., 1995a). Received
levels from the icebreaker playback
were estimated at 78–84 dB in the 1⁄3octave band centered at 5,000 Hz, or 8–
14 dB above ambient. If beluga whales
reacted to an actual icebreaker at
received levels of 80 dB, reactions
would be expected to occur at distances
on the order of 6.2 mi (10 km). Finley
et al. (1990) also reported beluga
avoidance of icebreaker activities in the
Canadian High Arctic at distances of
22–31 mi (35–50 km). In addition to
avoidance, changes in dive behavior and
pod integrity were also noted. However,
no icebreakers will be used during this
proposed program.
Patenaude et al. (2002) reported
changes in beluga whale diving and
respiration behavior, and some whales
veered away when a helicopter passed
at ≤820 ft (250 m) lateral distance at
altitudes up to 492 ft (150 m). However,
some belugas showed no reaction to the
helicopter. Belugas appeared to show
less response to fixed-wing aircraft than
to helicopter overflights.
In reviewing responses of cetaceans
with best hearing in mid-frequency
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ranges, which includes toothed whales,
Southall et al. (2007) reported that
combined field and laboratory data for
mid-frequency cetaceans exposed to
non-pulse sounds did not lead to a clear
conclusion about received levels
coincident with various behavioral
responses. In some settings, individuals
in the field showed profound
(significant) behavioral responses to
exposures from 90–120 dB, while others
failed to exhibit such responses for
exposure to received levels from 120–
150 dB. Contextual variables other than
exposure received level, and probable
species differences, are the likely
reasons for this variability. Context,
including the fact that captive subjects
were often directly reinforced with food
for tolerating noise exposure, may also
explain why there was great disparity in
results from field and laboratory
conditions—exposures in captive
settings generally exceeded 170 dB
before inducing behavioral responses. A
summary of some of the relevant
material reviewed by Southall et al.
(2007) is next.
Buckstaff (2004) reported elevated
dolphin whistle rates with received
levels from oncoming vessels in the 110
to 120 dB range in Sarasota Bay, Florida.
These hearing thresholds were
apparently lower than those reported by
a researcher listening with towed
hydrophones. Morisaka et al. (2005)
compared whistles from three
populations of Indo-Pacific bottlenose
dolphins. One population was exposed
to vessel noise with spectrum levels of
approximately 85 dB/Hz in the 1- to 22kHz band (broadband received levels
approximately 128 dB) as opposed to
approximately 65 dB/Hz in the same
band (broadband received levels
approximately 108 dB) for the other two
sites. Dolphin whistles in the noisier
environment had lower fundamental
frequencies and less frequency
modulation, suggesting a shift in sound
parameters as a result of increased
ambient noise.
Morton and Symonds (2002) used
census data on killer whales in British
Columbia to evaluate avoidance of nonpulse acoustic harassment devices
(AHDs). Avoidance ranges were about
2.5 mi (4 km). Also, there was a
dramatic reduction in the number of
days ‘‘resident’’ killer whales were
sighted during AHD-active periods
compared to pre- and post-exposure
periods and a nearby control site.
Monteiro-Neto et al. (2004) studied
avoidance responses of tucuxi (Sotalia
fluviatilis), a freshwater dolphin, to
Dukane® Netmark acoustic deterrent
devices. In a total of 30 exposure trials,
approximately five groups each
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demonstrated significant avoidance
compared to 20 pinger off and 55 nopinger control trials over two quadrats
of about 0.19 mi2 (0.5 km2). Estimated
exposure received levels were
approximately 115 dB.
Awbrey and Stewart (1983) played
back semi-submersible drillship sounds
(source level: 163 dB) to belugas in
Alaska. They reported avoidance
reactions at 984 and 4,921 ft (300 and
1,500 m) and approach by groups at a
distance of 2.2 mi (3.5 km; received
levels were approximately 110 to 145
dB over these ranges assuming a 15 log
R transmission loss). Similarly,
Richardson et al. (1990) played back
drilling platform sounds (source level:
163 dB) to belugas in Alaska. They
conducted aerial observations of eight
individuals among approximately 100
spread over an area several hundred
meters to several kilometers from the
sound source and found no obvious
reactions. Moderate changes in
movement were noted for three groups
swimming within 656 ft (200 m) of the
sound projector.
Two studies deal with issues related
to changes in marine mammal vocal
behavior as a function of variable
background noise levels. Foote et al.
(2004) found increases in the duration
of killer whale calls over the period
1977 to 2003, during which time vessel
traffic in Puget Sound, and particularly
whale-watching boats around the
animals, increased dramatically.
Scheifele et al. (2005) demonstrated that
belugas in the St. Lawrence River
increased the levels of their
vocalizations as a function of the
background noise level (the ‘‘Lombard
Effect’’).
Several researchers conducting
laboratory experiments on hearing and
the effects of non-pulse sounds on
hearing in mid-frequency cetaceans
have reported concurrent behavioral
responses. Nachtigall et al. (2003)
reported that noise exposures up to 179
dB and 55-min duration affected the
trained behaviors of a bottlenose
dolphin participating in a temporary
threshold shift (TTS) experiment.
Finneran and Schlundt (2004) provided
a detailed, comprehensive analysis of
the behavioral responses of belugas and
bottlenose dolphins to 1-s tones
(received levels 160 to 202 dB) in the
context of TTS experiments. Romano et
al. (2004) investigated the physiological
responses of a bottlenose dolphin and a
beluga exposed to these tonal exposures
and demonstrated a decrease in blood
cortisol levels during a series of
exposures between 130 and 201 dB.
Collectively, the laboratory observations
suggested the onset of a behavioral
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response at higher received levels than
did field studies. The differences were
likely related to the very different
conditions and contextual variables
between untrained, free-ranging
individuals vs. laboratory subjects that
were rewarded with food for tolerating
noise exposure.
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 move away
or maintain a somewhat greater distance
from the vessel when a large array of
airguns is operating than when it is
silent (e.g., Goold, 1996a,b,c;
Calambokidis and Osmek, 1998; Stone,
2003). 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 6.2–12.4 mi (10–20 km)
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 6.2–
12.4 mi (10–20 km) (Miller et al., 2005).
Observers stationed on seismic
vessels operating off the United
Kingdom from 1997–2000 have
provided data on the occurrence and
behavior of various toothed whales
exposed to seismic pulses (Stone, 2003;
Gordon et al., 2004). Killer whales were
found to be significantly farther from
large airgun arrays during periods of
shooting compared with periods of no
shooting. The displacement of the
median distance from the array was
approximately 0.5 km (0.3 mi) or more.
Killer whales also appear to be more
tolerant of seismic shooting in deeper
water.
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., 2002, 2005). However,
the animals tolerated high received
levels of sound (p–p level >200 dB re 1
m Pa) before exhibiting aversive
behaviors.
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Pinnipeds—Pinnipeds generally seem
to be less responsive to exposure to
industrial sound than most cetaceans.
Pinniped responses to underwater
sound from some types of industrial
activities such as seismic exploration
appear to be temporary and localized
(Harris et al., 2001; Reiser et al., 2009).
Southall et al. (2007) reviewed
literature describing responses of
pinnipeds to non-pulsed sound and
reported that the limited data suggest
exposures between approximately 90
and 140 dB generally do not appear to
induce strong behavioral responses in
pinnipeds exposed to non-pulse sounds
in water; no data exist regarding
exposures at higher levels. It is
important to note that among these
studies, there are some apparent
differences in responses between field
and laboratory conditions. In contrast to
the mid-frequency odontocetes, captive
pinnipeds responded more strongly at
lower levels than did animals in the
field. Again, contextual issues are the
likely cause of this difference.
Jacobs and Terhune (2002) observed
harbor seal reactions to AHDs (source
level in this study was 172 dB)
deployed around aquaculture sites.
Seals were generally unresponsive to
sounds from the AHDs. During two
specific events, individuals came within
141 and 144 ft (43 and 44 m) of active
AHDs and failed to demonstrate any
measurable behavioral response;
estimated received levels based on the
measures given were approximately 120
to 130 dB.
Costa et al. (2003) measured received
noise levels from an Acoustic
Thermometry of Ocean Climate (ATOC)
program sound source off northern
California using acoustic data loggers
placed on translocated elephant seals.
Subjects were captured on land,
transported to sea, instrumented with
archival acoustic tags, and released such
that their transit would lead them near
an active ATOC source (at 939-m depth;
75-Hz signal with 37.5-Hz bandwidth;
195 dB maximum source level, ramped
up from 165 dB over 20 min) on their
return to a haul-out site. Received
exposure levels of the ATOC source for
experimental subjects averaged 128 dB
(range 118 to 137) in the 60- to 90-Hz
band. None of the instrumented animals
terminated dives or radically altered
behavior upon exposure, but some
statistically significant changes in
diving parameters were documented in
nine individuals. Translocated northern
elephant seals exposed to this particular
non-pulse source began to demonstrate
subtle behavioral changes at exposure to
received levels of approximately 120 to
140 dB.
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Kastelein et al. (2006) exposed nine
captive harbor seals in an approximately
82 × 98 ft (25 × 30 m) enclosure to nonpulse sounds used in underwater data
communication systems (similar to
acoustic modems). Test signals were
frequency modulated tones, sweeps, and
bands of noise with fundamental
frequencies between 8 and 16 kHz; 128
to 130 [± 3] dB source levels; 1- to 2-s
duration [60–80 percent duty cycle]; or
100 percent duty cycle. They recorded
seal positions and the mean number of
individual surfacing behaviors during
control periods (no exposure), before
exposure, and in 15-min experimental
sessions (n = 7 exposures for each sound
type). Seals generally swam away from
each source at received levels of
approximately 107 dB, avoiding it by
approximately 16 ft (5 m), although they
did not haul out of the water or change
surfacing behavior. Seal reactions did
not appear to wane over repeated
exposure (i.e., there was no obvious
habituation), and the colony of seals
generally returned to baseline
conditions following exposure. The
seals were not reinforced with food for
remaining in the sound field.
Potential effects to pinnipeds from
aircraft activity could involve both
acoustic and non-acoustic effects. It is
uncertain if the seals react to the sound
of the helicopter or to its physical
presence flying overhead. Typical
reactions of hauled out pinnipeds to
aircraft that have been observed include
looking up at the aircraft, moving on the
ice or land, entering a breathing hole or
crack in the ice, or entering the water.
Ice seals hauled out on the ice have
been observed diving into the water
when approached by a low-flying
aircraft or helicopter (Burns and Harbo,
1972, cited in Richardson et al., 1995a;
Burns and Frost, 1979, cited in
Richardson et al., 1995a). Richardson et
al. (1995a) note that responses can vary
based on differences in aircraft type,
altitude, and flight pattern.
Blackwell et al. (2004a) observed 12
ringed seals during low-altitude
overflights of a Bell 212 helicopter at
Northstar in June and July 2000 (9
observations took place concurrent with
pipe-driving activities). One seal
showed no reaction to the aircraft while
the remaining 11 (92%) reacted, either
by looking at the helicopter (n=10) or by
departing from their basking site (n=1).
Blackwell et al. (2004a) concluded that
none of the reactions to helicopters were
strong or long lasting, and that seals
near Northstar in June and July 2000
probably had habituated to industrial
sounds and visible activities that had
occurred often during the preceding
winter and spring. There have been few
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systematic studies of pinniped reactions
to aircraft overflights, and most of the
available data concern pinnipeds hauled
out on land or ice rather than pinnipeds
in the water (Richardson et al., 1995a;
Born et al., 1999).
Reactions of harbor seals to the
simulated sound of a 2-megawatt wind
power generator were measured by
Koschinski et al. (2003). Harbor seals
surfaced significantly further away from
the sound source when it was active and
did not approach the sound source as
closely. The device used in that study
produced sounds in the frequency range
of 30 to 800 Hz, with peak source levels
of 128 dB at 1 m at the 80- and 160-Hz
frequencies.
Pinnipeds are not likely to show a
strong avoidance reaction to the airgun
sources proposed for use. Visual
monitoring from seismic vessels has
shown only slight (if any) avoidance of
airguns by pinnipeds and only slight (if
any) changes in behavior. Monitoring
work in the Alaskan Beaufort Sea during
1996–2001 provided considerable
information regarding the behavior of
Arctic ice seals exposed to seismic
pulses (Harris et al., 2001; Moulton and
Lawson, 2002). These seismic projects
usually involved arrays of 6 to 16
airguns with total volumes of 560 to
1,500 in3. The combined results suggest
that some seals avoid the immediate
area around seismic vessels. In most
survey years, ringed seal sightings
tended to be farther away from the
seismic vessel when the airguns were
operating than when they were not
(Moulton and Lawson, 2002). However,
these avoidance movements were
relatively small, on the order of 100 m
(328 ft) to a few hundreds of meters, and
many seals remained within 100–200 m
(328–656 ft) of the trackline as the
operating airgun array passed by. Seal
sighting rates at the water surface were
lower during airgun array operations
than during no-airgun periods in each
survey year except 1997. Similarly, seals
are often very tolerant of pulsed sounds
from seal-scaring devices (Mate and
Harvey, 1987; Jefferson and Curry, 1994;
Richardson et al., 1995a). 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 the species occurring in the
present study area are as strong as those
evident in the telemetry study, reactions
are expected to be confined to relatively
small distances and durations, with no
long-term effects on pinniped
individuals or populations.
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4. Threshold Shift (Noise-Induced Loss
of Hearing)
When animals exhibit reduced
hearing sensitivity (i.e., sounds must be
louder for an animal to detect them)
following exposure to an intense sound
or sound for long duration, it is referred
to as a noise-induced threshold shift
(TS). An animal can experience
temporary threshold shift (TTS) or
permanent threshold shift (PTS). TTS
can last from minutes or hours to days
(i.e., there is complete recovery), can
occur in specific frequency ranges (i.e.,
an animal might only have a temporary
loss of hearing sensitivity between the
frequencies of 1 and 10 kHz), and can
be of varying amounts (for example, an
animal’s hearing sensitivity might be
reduced initially by only 6 dB or
reduced by 30 dB). PTS is permanent,
but some recovery is possible. PTS can
also occur in a specific frequency range
and amount as mentioned above for
TTS.
The following physiological
mechanisms are thought to play a role
in inducing auditory TS: Effects to
sensory hair cells in the inner ear that
reduce their sensitivity, modification of
the chemical environment within the
sensory cells, residual muscular activity
in the middle ear, displacement of
certain inner ear membranes, increased
blood flow, and post-stimulatory
reduction in both efferent and sensory
neural output (Southall et al., 2007).
The amplitude, duration, frequency,
temporal pattern, and energy
distribution of sound exposure all can
affect the amount of associated TS and
the frequency range in which it occurs.
As amplitude and duration of sound
exposure increase, so, generally, does
the amount of TS, along with the
recovery time. For intermittent sounds,
less TS could occur than compared to a
continuous exposure with the same
energy (some recovery could occur
between intermittent exposures
depending on the duty cycle between
sounds) (Kryter et al., 1966; Ward,
1997). For example, one short but loud
(higher SPL) sound exposure may
induce the same impairment as one
longer but softer sound, which in turn
may cause more impairment than a
series of several intermittent softer
sounds with the same total energy
(Ward, 1997). Additionally, though TTS
is temporary, prolonged exposure to
sounds strong enough to elicit TTS, or
shorter-term exposure to sound levels
well above the TTS threshold, can cause
PTS, at least in terrestrial mammals
(Kryter, 1985). However, in the case of
the proposed exploratory drilling
program, animals are not expected to be
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exposed to levels high enough or
durations long enough to result in PTS.
PTS is considered auditory injury
(Southall et al., 2007). Irreparable
damage to the inner or outer cochlear
hair cells may cause PTS; however,
other mechanisms are also involved,
such as exceeding the elastic limits of
certain tissues and membranes in the
middle and inner ears and resultant
changes in the chemical composition of
the inner ear fluids (Southall et al.,
2007).
Although the published body of
scientific literature contains numerous
theoretical studies and discussion
papers on hearing impairments that can
occur with exposure to a loud sound,
only a few studies provide empirical
information on the levels at which
noise-induced loss in hearing sensitivity
occurs in nonhuman animals. For
marine mammals, published data are
limited to the captive bottlenose
dolphin, beluga, harbor porpoise, and
Yangtze finless porpoise (Finneran et
al., 2000, 2002b, 2003, 2005a, 2007,
2010a, 2010b; Finneran and Schlundt,
2010; Lucke et al., 2009; Mooney et al.,
2009a, 2009b; Popov et al., 2011a,
2011b; Kastelein et al., 2012a; Schlundt
et al., 2000; Nachtigall et al., 2003,
2004). For pinnipeds in water, data are
limited to measurements of TTS in
harbor seals, an elephant seal, and
California sea lions (Kastak et al., 1999,
2005; Kastelein et al., 2012b).
Marine mammal hearing plays a
critical role in communication with
conspecifics, and interpretation of
environmental cues for purposes such
as predator avoidance and prey capture.
Depending on the degree (elevation of
threshold in dB), duration (i.e., recovery
time), and frequency range of TTS, and
the context in which it is experienced,
TTS can have effects on marine
mammals ranging from discountable to
serious (similar to those discussed in
auditory masking, below). For example,
a marine mammal may be able to readily
compensate for a brief, relatively small
amount of TTS in a non-critical
frequency range that occurs during a
time where ambient noise is lower and
there are not as many competing sounds
present. Alternatively, a larger amount
and longer duration of TTS sustained
during time when communication is
critical for successful mother/calf
interactions could have more serious
impacts. Also, depending on the degree
and frequency range, the effects of PTS
on an animal could range in severity,
although it is considered generally more
serious because it is a permanent
condition. Of note, reduced hearing
sensitivity as a simple function of aging
has been observed in marine mammals,
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as well as humans and other taxa
(Southall et al., 2007), so we can infer
that strategies exist for coping with this
condition to some degree, though likely
not without cost.
Given the higher level of sound
necessary to cause PTS as compared
with TTS, it is considerably less likely
that PTS would occur during the
proposed exploratory drilling program
in Cook Inlet. However, several of the
sound sources do not even emit sound
levels at levels high enough to
potentially even cause TTS.
5. Non-Auditory Physical Effects
Non-auditory physical effects might
occur in marine mammals exposed to
strong underwater 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, and other types of
organ or tissue damage. Some marine
mammal species (i.e., beaked whales)
may be especially susceptible to injury
and/or stranding when exposed to
strong pulsed sounds.
Classic stress responses begin when
an animal’s central nervous system
perceives a potential threat to its
homeostasis. That perception triggers
stress responses regardless of whether a
stimulus actually threatens the animal;
the mere perception of a threat is
sufficient to trigger a stress response
(Moberg, 2000; Sapolsky et al., 2005;
Seyle, 1950). Once an animal’s central
nervous system perceives a threat, it
mounts a biological response or defense
that consists of a combination of the
four general biological defense
responses: Behavioral responses;
autonomic nervous system responses;
neuroendocrine responses; or immune
responses.
In the case of many stressors, an
animal’s first and most economical (in
terms of biotic costs) response is
behavioral avoidance of the potential
stressor or avoidance of continued
exposure to a stressor. An animal’s
second line of defense to stressors
involves the sympathetic part of the
autonomic nervous system and the
classical ‘‘fight or flight’’ response,
which includes the cardiovascular
system, the gastrointestinal system, the
exocrine glands, and the adrenal
medulla to produce changes in heart
rate, blood pressure, and gastrointestinal
activity that humans commonly
associate with ‘‘stress.’’ These responses
have a relatively short duration and may
or may not have significant long-term
effects on an animal’s welfare.
An animal’s third line of defense to
stressors involves its neuroendocrine or
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sympathetic nervous systems; the
system that has received the most study
has been the hypothalmus-pituitaryadrenal system (also known as the HPA
axis in mammals or the hypothalamuspituitary-interrenal axis in fish and
some reptiles). Unlike stress responses
associated with the autonomic nervous
system, virtually all neuroendocrine
functions that are affected by stress—
including immune competence,
reproduction, metabolism, and
behavior—are regulated by pituitary
hormones. Stress-induced changes in
the secretion of pituitary hormones have
been implicated in failed reproduction
(Moberg, 1987; Rivier, 1995), altered
metabolism (Elasser et al., 2000),
reduced immune competence (Blecha,
2000), and behavioral disturbance.
Increases in the circulation of
glucocorticosteroids (cortisol,
corticosterone, and aldosterone in
marine mammals; see Romano et al.,
2004) have been equated with stress for
many years.
The primary distinction between
stress (which is adaptive and does not
normally place an animal at risk) and
distress is the biotic cost of the
response. During a stress response, an
animal uses glycogen stores that can be
quickly replenished once the stress is
alleviated. In such circumstances, the
cost of the stress response would not
pose a risk to the animal’s welfare.
However, when an animal does not have
sufficient energy reserves to satisfy the
energetic costs of a stress response,
energy resources must be diverted from
other biotic functions, which impair
those functions that experience the
diversion. For example, when mounting
a stress response diverts energy away
from growth in young animals, those
animals may experience stunted growth.
When mounting a stress response
diverts energy from a fetus, an animal’s
reproductive success and fitness will
suffer. In these cases, the animals will
have entered a pre-pathological or
pathological state which is called
‘‘distress’’ (sensu Seyle, 1950) or
‘‘allostatic loading’’ (sensu McEwen and
Wingfield, 2003). This pathological state
will last until the animal replenishes its
biotic reserves sufficient to restore
normal function. Note that these
examples involved a long-term (days or
weeks) stress response exposure to
stimuli.
Relationships between these
physiological mechanisms, animal
behavior, and the costs of stress
responses have also been documented
fairly well through controlled
experiment; because this physiology
exists in every vertebrate that has been
studied, it is not surprising that stress
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19263
responses and their costs have been
documented in both laboratory and freeliving animals (for examples see,
Holberton et al., 1996; Hood et al., 1998;
Jessop et al., 2003; Krausman et al.,
2004; Lankford et al., 2005; Reneerkens
et al., 2002; Thompson and Hamer,
2000). Although no information has
been collected on the physiological
responses of marine mammals to
anthropogenic sound exposure, studies
of other marine animals and terrestrial
animals would lead us to expect some
marine mammals to experience
physiological stress responses and,
perhaps, physiological responses that
would be classified as ‘‘distress’’ upon
exposure to anthropogenic sounds.
For example, Jansen (1998) reported
on the relationship between acoustic
exposures and physiological responses
that are indicative of stress responses in
humans (e.g., elevated respiration and
increased heart rates). Jones (1998)
reported on reductions in human
performance when faced with acute,
repetitive exposures to acoustic
disturbance. Trimper et al. (1998)
reported on the physiological stress
responses of osprey to low-level aircraft
noise while Krausman et al. (2004)
reported on the auditory and physiology
stress responses of endangered Sonoran
pronghorn to military overflights. Smith
et al. (2004a, 2004b) identified noiseinduced physiological transient stress
responses in hearing-specialist fish (i.e.,
goldfish) that accompanied short- and
long-term hearing losses. Welch and
Welch (1970) reported physiological
and behavioral stress responses that
accompanied damage to the inner ears
of fish and several mammals.
Hearing is one of the primary senses
marine mammals use to gather
information about their environment
and communicate with conspecifics.
Although empirical information on the
relationship between sensory
impairment (TTS, PTS, and acoustic
masking) on marine mammals remains
limited, we assume that reducing a
marine mammal’s ability to gather
information about its environment and
communicate with other members of its
species would induce stress, based on
data that terrestrial animals exhibit
those responses under similar
conditions (NRC, 2003) and because
marine mammals use hearing as their
primary sensory mechanism. Therefore,
we assume that acoustic exposures
sufficient to trigger onset PTS or TTS
would be accompanied by physiological
stress responses. Marine mammals
might experience stress responses at
received levels lower than those
necessary to trigger onset TTS. Based on
empirical studies of the time required to
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recover from stress responses (Moberg,
2000), NMFS also assumes that stress
responses could persist beyond the time
interval required for animals to recover
from TTS and might result in
pathological and pre-pathological states
that would be as significant as
behavioral responses to TTS. However,
as stated previously in this document,
the source level of the jack-up rig is not
loud enough to induce PTS or likely
even TTS.
Resonance effects (Gentry, 2002) and
direct noise-induced bubble formations
(Crum et al., 2005) are implausible in
the case of exposure to an impulsive
broadband source like an airgun array.
If seismic surveys disrupt diving
patterns of deep-diving species, this
might result in bubble formation and a
form of the bends, as speculated to
occur in beaked whales exposed to
sonar. However, there is no specific
evidence of this upon exposure to
airgun pulses. Additionally, no beaked
whale species occur in the proposed
project area.
In general, very little is known about
the potential for strong, anthropogenic
underwater sounds to cause nonauditory physical effects in marine
mammals. Such effects, if they occur at
all, would presumably be limited to
short distances and to activities that
extend over a prolonged period. The
available data do not allow
identification of a specific exposure
level above which non-auditory effects
can be expected (Southall et al., 2007)
or any meaningful quantitative
predictions of the numbers (if any) of
marine mammals that might be affected
in those ways. There is no definitive
evidence that any of these effects occur
even for marine mammals in close
proximity to large arrays of airguns,
which are not proposed for use during
this program. For the most part, only
low-level continuous sounds would be
produced during the exploratory
drilling program. In addition, marine
mammals that show behavioral
avoidance of industry activities,
including belugas and some pinnipeds,
are especially unlikely to incur nonauditory impairment or other physical
effects.
6. Stranding and Mortality
Marine mammals close to underwater
detonations of high explosive can be
killed or severely injured, and the
auditory organs are especially
susceptible to injury (Ketten et al., 1993;
Ketten, 1995). Airgun pulses are less
energetic and their peak amplitudes
have slower rise times. To date, there is
no evidence that serious injury, death,
or stranding by marine mammals can
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occur from exposure to airgun pulses,
even in the case of large airgun arrays.
Additionally, the airguns used during
VSP are used for short periods of time.
The continuous sounds produced by the
drill rig are also far less energetic.
It should be noted that strandings
related to sound exposure have not been
recorded for marine mammal species in
Cook Inlet. Beluga whale strandings in
Cook Inlet are not uncommon; however,
these events often coincide with
extreme tidal fluctuations (‘‘spring
tides’’) or killer whale sightings
(Shelden et al., 2003). For example, in
August 2012, a group of Cook Inlet
beluga whales stranded in the mud flats
of Turnagain Arm during low tide and
were able to swim free with the flood
tide. NMFS does not expect any marine
mammals will incur serious injury or
mortality in Cook Inlet or strand as a
result of the proposed exploratory
drilling program.
Vessel Impacts
Vessel activity and noise associated
with vessel activity will temporarily
increase in the action area during
Buccaneer’s exploratory drilling
program as a result of the operation of
a jack-up drill rig and the use of tow and
other support vessels. While under tow,
the rig and the tow vessels move at slow
speeds (2–4 knots). The support barges
supplying pipe to the drill rig can
typically run at 7–8 knots but may move
slower inside Cook Inlet. Based on this
information, NMFS does not anticipate
and does not propose to authorize take
from vessel strikes.
Odontocetes, such as beluga whales,
killer whales, and harbor porpoises,
often show tolerance to vessel activity;
however, they may react at long
distances if they are confined by ice,
shallow water, or were previously
harassed by vessels (Richardson et al.,
1995). Beluga whale response to vessel
noise varies greatly from tolerance to
extreme sensitivity depending on the
activity of the whale and previous
experience with vessels (Richardson et
al., 1995). Reactions to vessels depends
on whale activities and experience,
habitat, boat type, and boat behavior
(Richardson et al., 1995) and may
include behavioral responses, such as
altered headings or avoidance (Blane
and Jaakson, 1994; Erbe and Farmer,
2000); fast swimming; changes in
vocalizations (Lesage et al., 1999;
Scheifele et al., 2005); and changes in
dive, surfacing, and respiration patterns.
There are few data published on
pinniped responses to vessel activity,
and most of the information is anecdotal
(Richardson et al., 1995). Generally, sea
lions in water show tolerance to close
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and frequently approaching vessels and
sometimes show interest in fishing
vessels. They are less tolerant when
hauled out on land; however, they
rarely react unless the vessel approaches
within 100–200 m (330–660 ft; reviewed
in Richardson et al., 1995).
The addition of the jack-up rig and a
few support vessels and noise due to rig
and vessel operations associated with
the exploratory drilling program would
not be outside the present experience of
marine mammals in Cook Inlet,
although levels may increase locally.
Given the large number of vessels in
Cook Inlet and the apparent habituation
to vessels by Cook Inlet marine
mammals that may occur in the area,
vessel activity and noise is not expected
to have effects that could cause
significant or long-term consequences
for individual marine mammals or their
populations.
Oil Spill and Discharge Impacts
As noted above, the specified activity
involves the drilling of exploratory
wells and associated activities in upper
Cook Inlet during the 2014 open water
season. The primary stressors to marine
mammals that are reasonably expected
to occur will be acoustic in nature. The
likelihood of a large or very large oil
spill occurring during Buccaneer’s
proposed exploratory drilling program
is remote. Offshore oil spill records in
Cook Inlet during 1994–2011 show three
spills during oil exploration (ADNR
Division of Oil and Gas, 2011 unpub.
data): Two oil spills at the UNOCAL
Dillion Platform in June 2011 (two
gallons) and December 2001 (three
gallons); and one oil spill at the
UNOCAL Monopod Platform in January
2002 (one gallon). During this same time
period, 71 spills occurred offshore in
Cook Inlet during oil production. Most
spills ranged from 0.0011 to 1 gallon (42
spills), and only three spills were larger
than 200 gallons: 210 gallons in July
2001 at the Cook Inlet Energy Stewart
facility; 250 gallons in February 1998 at
the King Salmon platform; and 504
gallons in October 1999 at the UNOCAL
Dillion platform. All 71 crude oil spills
from the offshore platforms, both
exploration and production, totaled less
than 2,140 gallons. Based on historical
data, most oil spills have been small.
Moreover, during more than 60 years of
oil and gas exploration and
development in Cook Inlet, there has
not been a single oil well blowout,
making it difficult to assign a specific
risk factor to the possibility of such an
event in Cook Inlet. However, the
probability of such an event is thought
to be of extremely low probability.
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Buccaneer will have various measures
and protocols in place that will be
implemented to prevent oil releases
from the wellbore. Buccaneer has
planned formal routine rig maintenance
and surveillance checks, as well as
normal inspection and equipment
checks to be conducted on the jack-up
rig daily. The following steps will be in
place to prevent oil from entering the
water:
• Required inspections will follow
standard operating procedures.
• Personnel working on the rig will
be directed to report any unusual
conditions to appropriate personnel.
• Oily equipment will be regularly
wiped down with oil absorbent pads to
collect free oil. Drips and small spillage
from equipment will be controlled
through use of drip pans and oil
absorbent drop clothes.
• Oil absorbent materials used to
contain oil spills or seeps will be
collected and disposed of in sealed
plastic bags or metal drums and closed
containers.
• The platform surfaces will be kept
clean of waste materials and loose
debris on a daily basis.
• Remedial actions will be taken
when visual inspections indicate
deterioration of equipment (tanks) and/
or their control systems.
• Following remedial work, and as
appropriate, tests will be conducted to
determine that the systems function
correctly.
Drilling and completion fluids
provide primary well control during
drilling, work over, or completion
operations. These fluids are designed to
exert hydrostatic pressure on the
wellbore that exceeds the pore pressures
within the subsurface formations. This
prevents undesired fluid flow into the
wellbore. Surface mounted blowout
preventer (BOP) equipment provides
secondary well control. In the event that
primary well control is lost, this surface
equipment is used to contain the influx
of formation fluid and then safely
circulate it out of the wellbore.
The BOP is a large, specialized valve
used to seal, control, and monitor oil
and gas wells. BOPs come in variety of
styles, sizes, and pressure ratings. For
Cook Inlet, the BOP equipment used by
Buccaneer will consist of:
• Three BOPs pressure safety levels
of: (1) 5,000 pounds per square inch
(psi) (2) 10,000 psi, and (3) 15,000 psi;
• A minimum of three 35 cm (13 5⁄8
in), 10,000 psi WP ram type preventers;
• One 35 cm (13 5⁄8 in) annular
preventer;
• Choke and kill lines that provide
circulating paths from/to the choke
manifold;
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• A two choke manifold that allows
for safe circulation of well influxes out
of the well bore; and
• A hydraulic control system with
accumulator backup closing.
The wellhead, associated valves, and
control systems provide blowout
prevention during well production.
These systems provide several layers of
redundancy to ensure pressure
containment is maintained. Well control
planning is performed in accordance
with Alaska Oil and Gas Conservation
Commission (AOGCC) and Bureau of
Safety and Environment Enforcement
(BSEE) regulations. The operator’s
policies and recommended practices
are, at a minimum, equivalent to BSEE
regulations. BOP test drills are
performed on a frequent basis to ensure
the well will be shut in quickly and
properly. BOP testing procedures will
meet American Petroleum Institute
Recommended Practice No. 53 and
AOGCC specifications. The BOP tests
will be conducted with a nonfreezing
fluid when the ambient temperature
around the BOP stack is below 0 °C
(32 °F). Tests will be conducted at least
weekly and before drilling out the shoe
of each casing string. The AOGCC will
be contacted before each test is
conducted, and will be onsite during
BOP tests unless an inspection waiver is
approved.
Buccaneer developed an Oil
Discharge Prevention and Contingency
Plan (ODPCP). Alaska’s Department of
Environmental Conservation (ADEC)
approved Buccaneer’s ODPCP on
August 29, 2012. NMFS reviewed the
ODPCP during the ESA consultation
process and found that with
implementation of the safety features
mentioned above that the risk of an oil
spill was discountable.
Despite concluding that the risk of
serious injury or mortality from an oil
spill in this case is extremely remote,
NMFS has nonetheless evaluated the
potential effects of an oil spill on marine
mammals. While an oil spill is not a
component of Buccaneer’s specified
activity for which NMFS is proposing to
authorize take, potential impacts on
marine mammals from an oil spill are
discussed in more detail next.
1. Potential Effects of Oil on Cetaceans
The specific effects an oil spill would
have on cetaceans are not well known.
While mortality is unlikely, exposure to
spilled oil could lead to skin irritation,
baleen fouling (which might reduce
feeding efficiency), respiratory distress
from inhalation of hydrocarbon vapors,
consumption of some contaminated
prey items, and temporary displacement
from contaminated feeding areas. Geraci
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and St. Aubin (1990) summarize effects
of oil on marine mammals. The number
of cetaceans that might be contacted by
a spill would depend on the size,
timing, and duration of the spill and
where the oil is in relation to the
animals. Whales may not avoid oil
spills, and some have been observed
feeding within oil slicks (Goodale et al.,
1981).
There is no direct evidence that oil
spills, including the much studied Santa
Barbara Channel and Exxon Valdez
spills, have caused any deaths of
cetaceans (Geraci, 1990; Brownell, 1971;
Harvey and Dahlheim, 1994). It is
suspected that some individually
identified killer whales that disappeared
from Prince William Sound during the
time of the Exxon Valdez spill were
casualties of that spill. However, no
clear cause and effect relationship
between the spill and the disappearance
could be established (Dahlheim and
Matkin, 1994). The AT–1 pod of
transient killer whales that sometimes
inhabits Prince William Sound has
continued to decline after the Exxon
Valdez oil spill (EVOS). Matkin et al.
(2008) tracked the AB resident pod and
the AT–1 transient group of killer
whales from 1984 to 2005. The results
of their photographic surveillance
indicate a much higher than usual
mortality rate for both populations the
year following the spill (33% for AB
Pod and 41% for AT–1 Group) and
lower than average rates of increase in
the 16 years after the spill (annual
increase of about 1.6% for AB Pod
compared to an annual increase of about
3.2% for other Alaska killer whale
pods). In killer whale pods, mortality
rates are usually higher for nonreproductive animals and very low for
reproductive animals and adolescents
(Olesiuk et al., 1990, 2005; Matkin et al.,
2005). No effects on humpback whales
in Prince William Sound were evident
after the EVOS (von Ziegesar et al.,
1994). There was some temporary
displacement of humpback whales out
of Prince William Sound, but this could
have been caused by oil contamination,
boat and aircraft disturbance,
displacement of food sources, or other
causes.
Migrating gray whales were
apparently not greatly affected by the
Santa Barbara spill of 1969. There
appeared to be no relationship between
the spill and mortality of marine
mammals. The higher than usual counts
of dead marine mammals recorded after
the spill represented increased survey
effort and therefore cannot be
conclusively linked to the spill itself
(Brownell, 1971; Geraci, 1990). The
conclusion was that whales were either
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able to detect the oil and avoid it or
were unaffected by it (Geraci, 1990).
Schwake et al. (2013) studied two
populations of common bottlenose
dolphins in the Gulf of Mexico
following the Deepwater Horizon oil
spill to evaluate sublethal effects. They
conducted health assessments in
Barataria Bay, Louisiana, an area that
received heavy and prolonged oiling
and in a reference site, Sarasota Bay,
Florida, where oil was not observed.
Several disease conditions were noted
for the Barataria Bay dolphins,
including hypoadrenocorticism,
pulmonary abnormalities, and tooth loss
(Schwake et al., 2013). Even though
several of the observed health effects are
consistent with exposure to petroleum
hydrocarbons because the researchers
did not have prespill health data for the
Barataria Bay dolphins, they cannot rule
out that other pre-existing
environmental stressors made this
population particularly vulnerable to
effects from the oil spill (Schwake et al.,
2013).
Whales rely on a layer of blubber for
insulation, so oil would have little if
any effect on thermoregulation by
whales. Effects of oiling on cetacean
skin appear to be minor and of little
significance to the animal’s health
(Geraci, 1990). Histological data and
ultrastructural studies by Geraci and St.
Aubin (1990) showed that exposures of
skin to crude oil for up to 45 minutes
in four species of toothed whales had no
effect. They switched to gasoline and
applied the sponge up to 75 minutes.
This produced transient damage to
epidermal cells in whales. Subtle
changes were evident only at the cell
level. In each case, the skin damage
healed within a week. They concluded
that a cetacean’s skin is an effective
barrier to the noxious substances in
petroleum. These substances normally
damage skin by getting between cells
and dissolving protective lipids. In
cetacean skin, however, tight
intercellular bridges, vital surface cells,
and the extraordinary thickness of the
epidermis impeded the damage. The
authors could not detect a change in
lipid concentration between and within
cells after exposing skin from a whitesided dolphin to gasoline for 16 hours
in vitro.
Whales could ingest oil if their food
is contaminated, or oil could also be
absorbed through the respiratory tract.
Some of the ingested oil is voided in
vomit or feces but some is absorbed and
could cause toxic effects (Geraci, 1990).
When returned to clean water,
contaminated animals can depurate this
internal oil (Engelhardt, 1978, 1982). Oil
ingestion can decrease food assimilation
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of prey eaten (St. Aubin, 1988).
Cetaceans may swallow some oilcontaminated prey, but it likely would
be only a small part of their food. It is
not known if whales would leave a
feeding area where prey was abundant
following a spill. Some zooplankton
eaten by baleen whales consume oil
particles, and bioaccumulation can
result. Tissue studies by Geraci and St.
Aubin (1990) revealed low levels of
naphthalene in the livers and blubber of
baleen whales. This result suggests that
prey have low concentrations in their
tissues, or that baleen whales may be
able to metabolize and excrete certain
petroleum hydrocarbons. However,
baleen whale species are uncommon in
the location of Buccaneer’s proposed
well sites. Baleen whales are more likely
to be encountered in the lower Inlet
during rig towing, far away from the
drill sites. Whales exposed to an oil
spill are unlikely to ingest enough oil to
cause serious internal damage (Geraci
and St. Aubin, 1980, 1982), and this
kind of damage has not been reported
(Geraci, 1990).
Some cetaceans can detect oil and
sometimes avoid it, but others enter and
swim through slicks without apparent
effects (Geraci, 1990; Harvey and
Dahlheim, 1994). Bottlenose dolphins in
the Gulf of Mexico apparently could
detect and avoid slicks and mousse but
did not avoid light sheens on the surface
(Smultea and Wursig, 1995). After the
Regal Sword spill in 1979, various
species of baleen and toothed whales
were observed swimming and feeding in
areas containing spilled oil southeast of
Cape Cod, MA (Goodale et al., 1981).
For months following EVOS, there were
numerous observations of gray whales,
harbor porpoises, Dall’s porpoises, and
killer whales swimming through lightto-heavy crude-oil sheens (Harvey and
Dalheim, 1994, cited in Matkin et al.,
2008). However, if some of the animals
avoid the area because of the oil, then
the effects of the oiling would be less
severe on those individuals.
2. Potential Effects of Oil on Pinnipeds
Externally oiled phocid seals often
survive and become clean, but heavily
oiled seal pups and adults may die,
depending on the extent of oiling and
characteristics of the oil. Adult seals
may suffer some temporary adverse
effects, such as eye and skin irritation,
with possible infection (MMS, 1996).
Such effects may increase stress, which
could contribute to the death of some
individuals. There is a likelihood that
newborn seal pups, if contacted by oil,
would die from oiling through loss of
insulation and resulting hypothermia.
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Reports of the effects of oil spills have
shown that some mortality of seals may
have occurred as a result of oil fouling;
however, large scale mortality had not
been observed prior to the EVOS (St.
Aubin, 1990). Effects of oil on marine
mammals were not well studied at most
spills because of lack of baseline data
and/or the brevity of the post-spill
surveys. The largest documented impact
of a spill, prior to EVOS, was on young
seals in January in the Gulf of St.
Lawrence (St. Aubin, 1990). Brownell
and Le Boeuf (1971) found no marked
effects of oil from the Santa Barbara oil
spill on California sea lions or on the
mortality rates of newborn pups.
Intensive and long-term studies were
conducted after the EVOS in Alaska.
There may have been a long-term
decline of 36% in numbers of molting
harbor seals at oiled haul-out sites in
Prince William Sound following EVOS
(Frost et al., 1994a). However, in a
reanalysis of those data and additional
years of surveys, along with an
examination of assumptions and biases
associated with the original data,
Hoover-Miller et al. (2001) concluded
that the EVOS effect had been
overestimated. The decline in
attendance at some oiled sites was more
likely a continuation of the general
decline in harbor seal abundance in
Prince William Sound documented
since 1984 (Frost et al., 1999) rather
than a result of EVOS. The results from
Hoover-Miller et al. (2001) indicate that
the effects of EVOS were largely
indistinguishable from natural decline
by 1992. However, while Frost et al.
(2004) concluded that there was no
evidence that seals were displaced from
oiled sites, they did find that aerial
counts indicated 26% fewer pups were
produced at oiled locations in 1989 than
would have been expected without the
oil spill. Harbor seal pup mortality at
oiled beaches was 23% to 26%, which
may have been higher than natural
mortality, although no baseline data for
pup mortality existed prior to EVOS
(Frost et al., 1994a). There was no
conclusive evidence of spill effects on
Steller sea lions (Calkins et al., 1994).
Oil did not persist on sea lions
themselves (as it did on harbor seals),
nor did it persist on sea lion haul-out
sites and rookeries (Calkins et al., 1994).
Sea lion rookeries and haul out sites,
unlike those used by harbor seals, have
steep sides and are subject to high wave
energy (Calkins et al., 1994).
Adult seals rely on a layer of blubber
for insulation, and oiling of the external
surface does not appear to have adverse
thermoregulatory effects (Kooyman et
al., 1976, 1977; St. Aubin, 1990).
Contact with oil on the external surfaces
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can potentially cause increased stress
and irritation of the eyes of ringed seals
(Geraci and Smith, 1976; St. Aubin,
1990). These effects seemed to be
temporary and reversible, but continued
exposure of eyes to oil could cause
permanent damage (St. Aubin, 1990).
Corneal ulcers and abrasions,
conjunctivitis, and swollen nictitating
membranes were observed in captive
ringed seals placed in crude oil-covered
water (Geraci and Smith, 1976) and in
seals in the Antarctic after an oil spill
(Lillie, 1954).
Marine mammals can ingest oil if
their food is contaminated. Oil can also
be absorbed through the respiratory tract
(Geraci and Smith, 1976; Engelhardt et
al., 1977). Some of the ingested oil is
voided in vomit or feces but some is
absorbed and could cause toxic effects
(Engelhardt, 1981). When returned to
clean water, contaminated animals can
depurate this internal oil (Engelhardt,
1978, 1982, 1985). In addition, seals
exposed to an oil spill are unlikely to
ingest enough oil to cause serious
internal damage (Geraci and St. Aubin,
1980, 1982).
Although seals may have the
capability to detect and avoid oil, they
apparently do so only to a limited extent
(St. Aubin, 1990). Seals may abandon
the area of an oil spill because of human
disturbance associated with cleanup
efforts, but they are most likely to
remain in the area of the spill. One
notable behavioral reaction to oiling is
that oiled seals are reluctant to enter the
water, even when intense cleanup
activities are conducted nearby (St.
Aubin, 1990; Frost et al., 1994b, 2004).
Seals that are under natural stress,
such as lack of food or a heavy
infestation by parasites, could
potentially die because of the additional
stress of oiling (Geraci and Smith, 1976;
St. Aubin, 1990; Spraker et al., 1994).
Female seals that are nursing young
would be under natural stress, as would
molting seals. In both cases, the seals
would have reduced food stores and
may be less resistant to effects of oil
than seals that are not under some type
of natural stress. Seals that are not
under natural stress (e.g., fasting,
molting) would be more likely to
survive oiling. In general, seals do not
exhibit large behavioral or physiological
reactions to limited surface oiling or
incidental exposure to contaminated
food or vapors (St. Aubin, 1990;
Williams et al., 1994). Effects could be
severe if seals surface in heavy oil slicks
in leads or if oil accumulates near haulout sites (St. Aubin, 1990).
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Anticipated Effects on Marine Mammal
Habitat
Potential Impacts From Seafloor
Disturbance on Marine Mammal Habitat
The primary potential impacts to
marine mammals and other marine
species are associated with elevated
sound levels produced by the
exploratory drilling program (i.e. the
drill rig and the airguns). However,
other potential impacts are also possible
to the surrounding habitat from physical
disturbance, discharges, and an oil spill
(should one occur). This section
describes the potential impacts to
marine mammal habitat from the
specified activity. Because the marine
mammals in the area feed on fish and/
or invertebrates there is also information
on the species typically preyed upon by
the marine mammals in the area.
There is a possibility of seafloor
disturbance or increased turbidity in the
vicinity of the drill sites. Seafloor
disturbance could occur with bottom
founding of the drill rig legs and
anchoring system. These activities could
lead to direct effects on bottom fauna,
through either displacement or
mortality. Increase in suspended
sediments from seafloor disturbance
also has the potential to indirectly affect
bottom fauna and fish. The amount and
duration of disturbed or turbid
conditions will depend on sediment
material.
The potential direct habitat impact by
the Buccaneer drilling operation is
limited to the actual drill-rig footprint
defined as the area occupied and
enclosed by the drill-rig legs. The jackup rig will temporarily disturb up to
two offshore locations in upper Cook
Inlet, where the wells are proposed to be
drilled. Bottom disturbance would
occur in the area where the three legs of
the rig would be set down and where
the actual well would be drilled. The
jack-up drill rig footprint would occupy
three steel piles at 14 m (46 ft) diameter.
The well casing would be a 76 cm (30
in) diameter pipe extending from the
seafloor to the rig floor. The casing
would only be in place during drilling
activities at each potential well location.
The total area of disturbance was
calculated as 0.54 acres during the land
use permitting process. The collective 2acre footprint of the wells represents a
very small fraction of the 7,300 square
mile Cook Inlet surface area. Potential
damage to the Cook Inlet benthic
community will be limited to the actual
surface area of the three spud cans
(1,585 square feet each or 4,755 square
feet total) that form the ‘‘foot’’ of each
leg. Given the high tidal energy at the
well site locations, drilling footprints
are not expected to support benthic
communities equivalent to shallow
lower energy sites found in nearshore
waters where harbor seals mostly feed.
The presence of the drill rig is not
expected to result in direct loss of
marine mammal habitat.
Common Marine Mammal Prey in the
Proposed Drilling Area
Fish are the primary prey species for
marine mammals in upper Cook Inlet.
Beluga whales feed on a variety of fish,
shrimp, squid, and octopus (Burns and
Seaman, 1986). Common prey species in
Knik Arm include salmon, eulachon
and cod. Harbor seals feed on fish such
as pollock, cod, capelin, eulachon,
Pacific herring, and salmon, as well as
a variety of benthic species, including
crabs, shrimp, and cephalopods. Harbor
seals are also opportunistic feeders with
their diet varying with season and
location. The preferred diet of the
harbor seal in the Gulf of Alaska
consists of pollock, octopus, capelin,
eulachon, and Pacific herring (Calkins,
1989). Other prey species include cod,
flat fishes, shrimp, salmon, and squid
(Hoover, 1988). Harbor porpoises feed
primarily on Pacific herring, cod,
whiting (hake), pollock, squid, and
octopus (Leatherwood et al., 1982). In
the upper Cook Inlet area, harbor
porpoise feed on squid and a variety of
small schooling fish, which would
likely include Pacific herring and
eulachon (Bowen and Siniff, 1999;
NMFS, unpublished data). Killer whales
feed on either fish or other marine
mammals depending on genetic type
(resident versus transient respectively).
Killer whales in Knik Arm are typically
the transient type (Shelden et al., 2003)
and feed on beluga whales and other
marine mammals, such as harbor seal
and harbor porpoise. The Steller sea
lion diet consists of a variety of fishes
(capelin, cod, herring, mackerel,
pollock, rockfish, salmon, sand lance,
etc.), bivalves, squid, octopus, and
gastropods.
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Potential Impacts From Sound
Generation
With regard to fish as a prey source
for odontocetes and seals, fish are
known to hear and react to sounds and
to use sound to communicate (Tavolga
et al., 1981) and possibly avoid
predators (Wilson and Dill, 2002).
Experiments have shown that fish can
sense both the strength and direction of
sound (Hawkins, 1981). Primary factors
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determining whether a fish can sense a
sound signal, and potentially react to it,
are the frequency of the signal and the
strength of the signal in relation to the
natural background noise level.
Fishes produce sounds that are
associated with behaviors that include
territoriality, mate search, courtship,
and aggression. It has also been
speculated that sound production may
provide the means for long distance
communication and communication
under poor underwater visibility
conditions (Zelick et al., 1999), although
the fact that fish communicate at lowfrequency sound levels where the
masking effects of ambient noise are
naturally highest suggests that very long
distance communication would rarely
be possible. Fishes have evolved a
diversity of sound generating organs and
acoustic signals of various temporal and
spectral contents. Fish sounds vary in
structure, depending on the mechanism
used to produce them (Hawkins, 1993).
Generally, fish sounds are
predominantly composed of low
frequencies (less than 3 kHz).
Since objects in the water scatter
sound, fish are able to detect these
objects through monitoring the ambient
noise. Therefore, fish are probably able
to detect prey, predators, conspecifics,
and physical features by listening to
environmental sounds (Hawkins, 1981).
There are two sensory systems that
enable fish to monitor the vibrationbased information of their surroundings.
The two sensory systems, the inner ear
and the lateral line, constitute the
acoustico-lateralis system.
Although the hearing sensitivities of
very few fish species have been studied
to date, it is becoming obvious that the
intra- and inter-specific variability is
considerable (Coombs, 1981). Nedwell
et al. (2004) compiled and published
available fish audiogram information. A
noninvasive electrophysiological
recording method known as auditory
brainstem response is now commonly
used in the production of fish
audiograms (Yan, 2004). Generally, most
fish have their best hearing in the lowfrequency range (i.e., less than 1 kHz).
Even though some fish are able to detect
sounds in the ultrasonic frequency
range, the thresholds at these higher
frequencies tend to be considerably
higher than those at the lower end of the
auditory frequency range.
Literature relating to the impacts of
sound on marine fish species can be
divided into the following categories: (1)
Pathological effects; (2) physiological
effects; and (3) behavioral effects.
Pathological effects include lethal and
sub-lethal physical damage to fish;
physiological effects include primary
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and secondary stress responses; and
behavioral effects include changes in
exhibited behaviors of fish. Behavioral
changes might be a direct reaction to a
detected sound or a result of the
anthropogenic sound masking natural
sounds that the fish normally detect and
to which they respond. The three types
of effects are often interrelated in
complex ways. For example, some
physiological and behavioral effects
could potentially lead to the ultimate
pathological effect of mortality. Hastings
and Popper (2005) reviewed what is
known about the effects of sound on
fishes and identified studies needed to
address areas of uncertainty relative to
measurement of sound and the
responses of fishes. Popper et al. (2003/
2004) also published a paper that
reviews the effects of anthropogenic
sound on the behavior and physiology
of fishes.
Potential effects of exposure to
continuous sound on marine fish
include TTS, physical damage to the ear
region, physiological stress responses,
and behavioral responses such as startle
response, alarm response, avoidance,
and perhaps lack of response due to
masking of acoustic cues. Most of these
effects appear to be either temporary or
intermittent and therefore probably do
not significantly impact the fish at a
population level. The studies that
resulted in physical damage to the fish
ears used noise exposure levels and
durations that were far more extreme
than would be encountered under
conditions similar to those expected
during Buccaneer’s proposed
exploratory drilling activities.
The level of sound at which a fish
will react or alter its behavior is usually
well above the detection level. Fish
have been found to react to sounds
when the sound level increased to about
20 dB above the detection level of 120
dB (Ona, 1988); however, the response
threshold can depend on the time of
year and the fish’s physiological
condition (Engas et al., 1993). In
general, fish react more strongly to
pulses of sound rather than a
continuous signal (Blaxter et al., 1981),
such as the type of sound that will be
produced by the drillship, and a quicker
alarm response is elicited when the
sound signal intensity rises rapidly
compared to sound rising more slowly
to the same level.
Investigations of fish behavior in
relation to vessel noise (Olsen et al.,
1983; Ona, 1988; Ona and Godo, 1990)
have shown that fish react when the
sound from the engines and propeller
exceeds a certain level. Avoidance
reactions have been observed in fish
such as cod and herring when vessels
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approached close enough that received
sound levels are 110 dB to 130 dB
(Nakken, 1992; Olsen, 1979; Ona and
Godo, 1990; Ona and Toresen, 1988).
However, other researchers have found
that fish such as polar cod, herring, and
capeline are often attracted to vessels
(apparently by the noise) and swim
toward the vessel (Rostad et al., 2006).
Typical sound source levels of vessel
noise in the audible range for fish are
150 dB to 170 dB (Richardson et al.,
1995a). (Based on models, the 160 dB
radius for the jack-up rig would extend
approximately 33 ft [10 m]; therefore,
fish would need to be in close proximity
to the drill rig for the noise to be
audible). In calm weather, ambient
noise levels in audible parts of the
spectrum lie between 60 dB to 100 dB.
Buccaneer also proposes to conduct
VSP surveys with an airgun array for a
short period of time during the drilling
season (only a few hours over 1–2 days
per well over the course of the entire
proposed drilling program). Airguns
produce impulsive sounds as opposed
to continuous sounds at the source.
Short, sharp sounds can cause overt or
subtle changes in fish behavior.
Chapman and Hawkins (1969) tested the
reactions of whiting (hake) in the field
to an airgun. When the airgun was fired,
the fish dove from 82 to 180 ft (25 to 55
m) depth and formed a compact layer.
The whiting dove when received sound
levels were higher than 178 dB re 1 mPa
(Pearson et al., 1992).
Pearson et al. (1992) conducted a
controlled experiment to determine
effects of strong noise pulses on several
species of rockfish off the California
coast. They used an airgun with a
source level of 223 dB re 1 mPa. They
noted:
• Startle responses at received levels
of 200–205 dB re 1 mPa and above for
two sensitive species, but not for two
other species exposed to levels up to
207 dB;
• Alarm responses at 177–180 dB for
the two sensitive species, and at 186 to
199 dB for other species;
• An overall threshold for the above
behavioral response at about 180 dB;
• An extrapolated threshold of about
161 dB for subtle changes in the
behavior of rockfish; and
• A return to pre-exposure behaviors
within the 20–60 minute exposure
period.
In summary, fish often react to
sounds, especially strong and/or
intermittent sounds of low frequency.
Sound pulses at received levels of 160
dB re 1 mPa may cause subtle changes
in behavior. Pulses at levels of 180 dB
may cause noticeable changes in
behavior (Chapman and Hawkins, 1969;
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Pearson et al., 1992; Skalski et al.,
1992). It also appears that fish often
habituate to repeated strong sounds
rather rapidly, on time scales of minutes
to an hour. However, the habituation
does not endure, and resumption of the
strong sound source may again elicit
disturbance responses from the same
fish. Underwater sound levels from the
drill rig and other vessels produce
sounds lower than the response
threshold reported by Pearson et al.
(1992), and are not likely to result in
major effects to fish near the proposed
drill sites.
Based on a sound level of
approximately 140 dB, there may be
some avoidance by fish of the area near
the jack-up while drilling, around the
rig under tow, and around other support
and supply vessels when underway.
Any reactions by fish to these sounds
will last only minutes (Mitson and
Knudsen, 2003; Ona et al., 2007) longer
than the vessel is operating at that
location or the drill rig is drilling. Any
potential reactions by fish would be
limited to a relatively small area within
about 33 ft (10 m) of the drill rig during
drilling. Avoidance by some fish or fish
species could occur within portions of
this area.
The lease areas do not support major
populations of cod, Pollock, and sole,
although all four salmon species and
smelt migrate through the area to
spawning rivers in upper Cook Inlet
(Shields and Dupuis, 2012). Residency
time for the migrating finfish in the
vicinity of an operating platform would
be short-term, limiting fish exposure to
noise associated with the proposed
drilling program.
Some of the fish species found in
Cook Inlet are prey sources for
odontocetes and pinnipeds. A reaction
by fish to sounds produced by
Buccaneer’s proposed operations would
only be relevant to marine mammals if
it caused concentrations of fish to vacate
the area. Pressure changes of sufficient
magnitude to cause that type of reaction
would probably occur only very close to
the sound source, if any would occur at
all due to the low energy sounds
produced by the majority of equipment
proposed for use. Impacts on fish
behavior are predicted to be
inconsequential. Thus, feeding
odontocetes and pinnipeds would not
be adversely affected by this minimal
loss or scattering, if any, which is not
expected to result in reduced prey
abundance. The proposed drilling area
is not a common feeding area for baleen
whales.
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Potential Impacts From Drilling
Discharges
The drill rig Endeavour will operate
under the Alaska Pollutant Discharge
Elimination System (APDES) general
permit AKG–31–5021 for wastewater
discharges (ADEC, 2012). This permit
authorizes discharges from oil and gas
extraction facilities engaged in
exploration under the Offshore and
Coastal Subcategories of the Oil and Gas
Extraction Point Source Category (40
CFR Part 435). Twelve effluents are
authorized for discharge into Cook Inlet
once ADEC discharge limits have been
met. The authorized discharges include:
Drilling fluids and drill cuttings, deck
drainage, sanitary waste, domestic
waste, blowout preventer fluid, boiler
blow down, fire control system test
water, uncontaminated ballast water,
bilge water, excess cement slurry, mud
cuttings cement at sea floor, and
completion fluids. Areas prohibited
from discharge in the Cook Inlet are 10meter (33-foot) isobaths, 5-meter (16foot) isobaths, and other geographic area
restrictions (AKG–31–5021.I.C.). The
Endeavour is also authorized under
EPA’s Vessel General Permit for deck
wash down and runoff, gray water, and
gray water mixed with sewage
discharges. The effluent limits and
related requirements for these
discharges in the Vessel General Permit
are to minimize or eliminate to the
extent achievable using control
measures (best management practices)
(EPA, 2011).
Drilling wastes include drilling fluids,
known as mud, rock cuttings, and
formation waters. Drilling wastes (nonhydrocarbon) will be discharged to the
Cook Inlet under the approved APDES
general permit. Drilling wastes
(hydrocarbon) will be delivered to an
onshore permitted location for disposal.
During drilling, the onsite tool pusher/
driller and qualified mud engineers will
direct and maintain desired mud
properties, and maintain the quantities
of basic mud materials on site as
dictated by good oilfield practice.
Buccaneer will follow best management
practices to ensure that a sufficient
inventory of barite and lost circulation
materials are maintained on the drilling
vessel to minimize the possibility of a
well upset and the likelihood of a
release of pollutants to Cook Inlet
waters. These materials can be resupplied, if required, using the supply
vessel. Because adverse weather could
prevent immediate re-supply, sufficient
materials will be available on board to
completely rebuild the total circulating
volume. Buccaneer will conduct an
Environmental Monitoring Study of
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relevant hydrographic, sediment
hydrocarbon, and heavy metal data from
surveys conducted before and during
drilling mud disposal and up to a least
one year after drilling operations cease
in accordance with the APDES general
permit for discharges of drilling muds
and cuttings.
Non-drilling wastewater includes
deck drainage, sanitary waste, domestic
waste, blowout preventer fluid, boiler
blow down, fire control test water, bilge
water, non-contact cooling water, and
uncontaminated ballast water. Nondrilling wastewater will be discharged
into Cook Inlet under the approved
APDES general permit or delivered to an
onshore permitted location for disposal.
Mud cuttings will be constantly tested.
No hydrocarboned muds will be
permitted to be discharged into Cook
Inlet. They will be hauled offsite. Solid
waste (e.g., packaging, domestic trash)
will be classified, segregated, and
labeled as general, universal, and
Resource Conservation and Recovery
Act exempt or non-exempt waste. It will
be stored in containers at designated
accumulation areas. Then, it will be
packaged and palletized for transport to
an approved on-shore disposal facility.
No hazardous wastes should not be
generated as a result of this project.
However, if any hazardous wastes were
generated, it would be temporarily
stored in an onboard satellite
accumulation area and then transported
offsite for disposal at an approved
facility.
With oil and gas platforms presently
operating in Cook Inlet, there is concern
for continuous exposure to potentially
toxic heavy metals and metalloids (i.e.,
mercury, lead, cadmium, copper, zinc,
and arsenic) that are associated with oil
and gas development and production.
These elements occur naturally in the
earths’ crust and the oceans but many
also have anthropogenic origins from
local sources of pollution or from
contamination from atmospheric
distribution.
Discharging drill cuttings or other
liquid waste streams generated by the
drilling vessel could potentially affect
marine mammal habitat. Toxins could
persist in the water column, which
could have an impact on marine
mammal prey species. However, despite
a considerable amount of investment in
research on exposures of marine
mammals to organochlorines or other
toxins, there have been no marine
mammal deaths in the wild that can be
conclusively linked to the direct
exposure to such substances (O’Shea,
1999).
Drilling muds and cuttings discharged
to the seafloor can lead to localized
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increased turbidity and increase in
background concentrations of barium
and occasionally other metals in
sediments and may affect lower trophic
organisms. Drilling muds are composed
primarily of bentonite (clay), and the
toxicity is therefore low. Heavy metals
in the mud may be absorbed by benthic
organisms, but studies have shown that
heavy metals do not bio-magnify in
marine food webs (Neff et al., 1989).
Effects on benthic communities are
nearly always restricted to a zone within
about 328 to 492 ft (100 to 150 m) of the
discharge, where cuttings
accumulations are greatest. Discharges
and drill cuttings could impact fish by
displacing them from the affected area.
Beluga whales analyzed for heavy
metals and other elements (cadmium,
mercury, selenium, vanadium, and
silver) were generally lower in the livers
of Cook Inlet animals than in the other
beluga whale stocks, while copper was
higher (Becker et al., 2001). Hepatic
methyl mercury levels were similar to
those reported for other beluga whales
(Geraci and St. Aubin, 1990). The
relatively high hepatic concentration of
silver found in the eastern Chukchi Sea
and Beaufort Sea stocks of belugas was
also found in the Cook Inlet animals,
suggesting a species-specific
phenomenon. However, because of the
limited discharges no water quality
impacts are anticipated that would
negatively affect habitat for Cook Inlet
marine mammals.
Potential Impacts From Drill Rig
Presence
The horizontal dimensions of the
jack-up rig are 160 ft by 35 ft (48.8 m
by 10.7 m). The dimensions of the drill
rig (less than one football field on either
side) are not significant enough to cause
a large-scale diversion from the animals’
normal swim and migratory paths. Any
deflection of marine mammal species
due to the physical presence of the drill
rig would be very minor. The drill rig’s
physical footprint is small relative to the
size of the geographic region it will
occupy and will likely not cause marine
mammals to deflect greatly from their
typical migratory route. Also, even if
animals may deflect because of the
presence of the drill rig, Cook Inlet is
much larger in size than the length of
the drill rig (many dozens of miles vs.
less than one football field), and animals
would have other means of passage
around the drill rig. In sum, the physical
presence of the drill rig is not likely to
cause a significant deflection to
migrating marine mammals.
Potential Impacts From an Oil Spill
Lower trophic organisms and fish
species are primary food sources for
marine mammals likely to be found in
the proposed project vicinity. Any
diminishment of feeding habitat during
the summer months due to an oil spill
or response could affect the energy
balance of marine mammals. If oil found
its way into upper Cook Inlet in the area
of the Susitna and Little Susitna rivers
during the summer months, a large
portion of Cook Inlet beluga whale Area
1 critical habitat could be impacted. If
an oil spill were to occur later in the
season, it could become trapped in or
under the ice or travel with the thinner
ice pans.
Due to their wide distribution, large
numbers, and rapid rate of regeneration,
the recovery of marine invertebrate
populations is expected to occur soon
after the surface oil passes. Spill
response activities are not likely to
disturb the prey items of whales or seals
sufficiently to cause more than minor
effects. Spill response activities could
cause marine mammals to avoid the
disturbed habitat that is being cleaned.
However, by causing avoidance, animals
would avoid impacts from the oil itself.
Additionally, the likelihood of an oil
spill is expected to be very low, as
discussed earlier in this document.
Based on the preceding discussion of
potential types of impacts to marine
mammal habitat, overall, the proposed
specified activity is not expected to
cause significant impacts on habitats
used by the marine mammal species in
the proposed project area or on the food
sources that they utilize.
Proposed Mitigation
In order to issue an incidental take
authorization (ITA) under section
101(a)(5)(D) of the MMPA, NMFS must
set forth the permissible methods of
taking pursuant to such activity, and
other means of effecting the least
practicable impact on such species or
stock and its habitat, paying particular
attention to rookeries, mating grounds,
and areas of similar significance, and on
the availability of such species or stock
for taking for certain subsistence uses
(where relevant). Later in this document
in the ‘‘Proposed Incidental Harassment
Authorization’’ section, NMFS lays out
the proposed conditions for review, as
they would appear in the final IHA (if
issued).
While the drill rig does not emit
sound levels that require shutdowns to
avoid Level A harassment (injury),
because take of beluga whales is not
authorized, shutdown procedures will
be required to avoid Level B take of this
species. For continuous sounds, such as
those produced by drilling operations
and rig tow, NMFS uses a received level
of 120-dB (rms) to indicate the onset of
Level B harassment. For impulse
sounds, such as those produced by the
airgun array during the VSP surveys or
the impact hammer during conductor
pipe driving, NMFS uses a received
level of 160-dB (rms) to indicate the
onset of Level B harassment. The
current Level A (injury) harassment
threshold is 180 dB (rms) for cetaceans
and 190 dB (rms) for pinnipeds. Table
1 in this document outlines the various
applicable radii for which different
mitigation measures would apply.
TABLE 1—APPLICABLE MITIGATION AND SHUTDOWN RADII FOR BUCCANEER’S PROPOSED UPPER COOK INLET
EXPLORATORY DRILLING PROGRAM
190 dB radius
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Impact hammer during conductor pipe driving ....................................
Airguns during VSP .............................................................................
Rig tow .................................................................................................
Deep well pumps on the jack-up rig ....................................................
180 dB radius
160 dB radius
120 dB radius
60 m (200 ft) .....
75 m (246 ft) .....
NA ....................
NA ....................
250 m (820 ft) ...
240 m (787 ft) ...
NA .....................
NA ....................
2 km (1.24 mi) ..
2.5 km (1.55 mi)
NA ....................
NA .....................
NA.
NA.
600 m (2,000 ft).
260 m (853 ft).
Rig tow source levels do not exceed 171 dB (rms); Jack-up rig source levels without deep well pumps is below ambient sound levels; NA =
Not applicable.
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Mitigation Measures Proposed by
Buccaneer
For the proposed mitigation measures,
Buccaneer listed the following protocols
to be implemented during its
exploratory drilling program in Cook
Inlet.
1. Conductor Pipe Driving Measures
Protected species observers (PSOs)
will observe from the drill rig during
this 2–3 day portion of the proposed
program out to the 160 dB (rms) radius
of 2 km (1.24 mi). If marine mammal
species for which take is not authorized
enter this zone, then use of the impact
hammer will cease. If cetaceans for
which take is authorized enter within
the 180 dB (rms) radius of 250 m (820
ft) or if pinnipeds for which take is
authorized enter within the 190 dB
(rms) radius of 60 m (200 ft), then use
of the impact hammer will cease.
Following a shutdown of impact
hammering activities, the applicable
zones must be clear of marine mammals
for at least 30 minutes prior to restarting
activities.
Buccaneer proposes to follow a rampup procedure during impact hammering
activities. PSOs will visually monitor
out to the 160 dB radius for at least 30
minutes prior to the initiation of
activities. If no marine mammals are
detected during that time, then
Buccaneer can initiate impact
hammering using a ‘‘soft start’’
technique. Hammering will begin with
an initial set of three strikes at 40
percent energy followed by a 1 min
waiting period, then two subsequent
three-strike sets. This ‘‘soft-start’’
procedure will be implemented anytime
impact hammering has ceased for 30
minutes or more. Impact hammer ‘‘softstart’’ will not be required if the
hammering downtime is for less than 30
minutes and visuals surveys are
continued throughout the silent period
and no marine mammals are observed in
the applicable zones during that time.
Monitoring will occur during all
hammering sessions.
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2. VSP Airgun Measures
PSOs will observe from the drill rig
during this 1–2 day portion of the
proposed program out to the 160 dB
radius of 2.5 km (1.55 mi). If marine
mammal species for which take is not
authorized enter this zone, then use of
the airguns will cease. If cetaceans for
which take is authorized enter within
the 180 dB (rms) radius of 240 m (787
ft) or if pinnipeds for which take is
authorized enter within the 190 dB
(rms) radius of 75 m (246 ft), then use
of the airguns will cease. Following a
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shutdown of airgun operations, the
applicable zones must be clear of
marine mammals for at least 30 minutes
prior to restarting activities.
Buccaneer proposes to follow a rampup procedure during airgun operations.
PSOs will visually monitor out to the
160 dB radius for at least 30 minutes
prior to the initiation of activities. If no
marine mammals are detected during
that time, then Buccaneer can initiate
airgun operations using a ‘‘ramp-up’’
technique. Airgun operations will begin
with the firing of a single airgun, which
will be the smallest gun in the array in
terms of energy output (dB) and volume
(in3). Operators will then continue
ramp-up by gradually activating
additional airguns over a period of at
least 30 minutes (but not longer than 40
minutes) until the desired operating
level of the airgun array is obtained.
This ramp-up procedure will be
implemented anytime airguns have not
been fired for 30 minutes or more.
Airgun ramp-up will not be required if
the airguns have been off for less than
30 minutes and visuals surveys are
continued throughout the silent period
and no marine mammals are observed in
the applicable zones during that time.
Monitoring will occur during all airgun
usage.
3. Rig Tow and Drill Rig Operation
As mentioned previously, these
activities do not generate sounds that
require implementation of mitigation
measures to avoid injury. However,
PSOs will be stationed on the helicopter
platform (bow) of the drill rig
(positioned about 100 ft above the
waterline) to watch for marine
mammals. With the exception of the
operation of the deep-well pump on the
jack-up rig, the other machinery
generates sound levels below ambient.
PSOs will observe from the drill rig
during this portion of the proposed
program out to the 120 dB radius of 260
m (853 ft). If marine mammal species for
which take is not authorized enter this
zone, then the deep well pumps will be
turned off. The PSOs will operate from
multiple stations on the rig, recognizing
that the shutdown radius begins from
the submersed pump housed inside the
forward jack-up leg.
4. Oil Spill Plan
Buccaneer developed an ODPCP.
ADEC approved Buccaneer’s ODPCP on
August 29, 2012. NMFS reviewed the
ODPCP during the ESA consultation
process and found that with
implementation of the safety features
mentioned above that the risk of an oil
spill was discountable.
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5. Pollution Discharge Plan
When the drill rig is towed or
otherwise floating it is classified as a
vessel (like a barge). During those
periods, it is covered under a form of
National Pollutant Discharge
Elimination System permit known as a
Vessel General Permit. This permit
remains federal and is a ‘‘no discharge
permit,’’ which allows for the discharge
of storm water and closed system fire
suppression water but no other
effluents.
When the legs are down, the drill rig
becomes a facility. During those periods,
it is covered under an approved APDES.
Under the APDES, certain discharges
are permitted. However, Buccaneer is
not permitted to discharge gray water,
black water, or hydrocarboned muds.
They are all hauled off and not
discharged.
Mitigation Measures Proposed by NMFS
NMFS proposes that when Buccaneer
utilizes helicopters for support
operations that the helicopters must
maintain an altitude of at least 1,000 ft
(305 m), except during takeoffs,
landings, or emergency situations.
Mitigation Conclusions
NMFS has carefully evaluated
Buccaneer’s proposed mitigation
measures and considered a range of
other measures in the context of
ensuring that NMFS prescribes the
means of effecting the least practicable
impact on the affected marine mammal
species and stocks and their habitat. Our
evaluation of potential measures
included consideration of the following
factors in relation to one another:
• The manner in which, and the
degree to which, the successful
implementation of the measures are
expected to minimize adverse impacts
to marine mammals;
• The proven or likely efficacy of the
specific measure to minimize adverse
impacts as planned; and
• The practicability of the measure
for applicant implementation.
Any mitigation measure(s) prescribed
by NMFS should be able to accomplish,
have a reasonable likelihood of
accomplishing (based on current
science), or contribute to the
accomplishment of one or more of the
general goals listed below:
1. Avoidance or minimization of
injury or death of marine mammals
wherever possible (goals 2, 3, and 4 may
contribute to this goal).
2. A reduction in the numbers of
marine mammals (total number or
number at biologically important time
or location) exposed to received levels
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of seismic airguns, impact hammers,
drill rig deep well pumps, or other
activities expected to result in the take
of marine mammals (this goal may
contribute to 1, above, or to reducing
harassment takes only).
3. A reduction in the number of times
(total number or number at biologically
important time or location) individuals
would be exposed to received levels of
seismic airguns impact hammers, drill
rig deep well pumps, or other activities
expected to result in the take of marine
mammals (this goal may contribute to 1,
above, or to reducing harassment takes
only).
4. A reduction in the intensity of
exposures (either total number or
number at biologically important time
or location) to received levels of seismic
airguns impact hammers, drill rig deep
well pumps, or other activities expected
to result in the take of marine mammals
(this goal may contribute to 1, above, or
to reducing the severity of harassment
takes only).
5. Avoidance or minimization of
adverse effects to marine mammal
habitat, paying special attention to the
food base, activities that block or limit
passage to or from biologically
important areas, permanent destruction
of habitat, or temporary destruction/
disturbance of habitat during a
biologically important time.
6. For monitoring directly related to
mitigation—an increase in the
probability of detecting marine
mammals, thus allowing for more
effective implementation of the
mitigation.
Based on our evaluation of the
applicant’s proposed measures, as well
as other measures considered by NMFS,
NMFS has preliminarily determined
that the proposed mitigation measures
provide the means of effecting the least
practicable impact on marine mammals
species or stocks and their habitat,
paying particular attention to rookeries,
mating grounds, and areas of similar
significance.
Proposed Monitoring and Reporting
In order to issue an ITA for an
activity, section 101(a)(5)(D) of the
MMPA states that NMFS must set forth
‘‘requirements pertaining to the
monitoring and reporting of such
taking’’. The MMPA implementing
regulations at 50 CFR 216.104 (a)(13)
indicate that requests for ITAs must
include the suggested means of
accomplishing the necessary monitoring
and reporting that will result in
increased knowledge of the species and
of the level of taking or impacts on
populations of marine mammals that are
expected to be present in the proposed
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action area. Buccaneer submitted
information regarding marine mammal
monitoring to be conducted during
seismic operations as part of the IHA
application. That information can be
found in Appendix C of the application.
The monitoring measures may be
modified or supplemented based on
comments or new information received
from the public during the public
comment period.
Monitoring measures proposed by the
applicant or prescribed by NMFS
should accomplish one or more of the
following top-level goals:
1. An increase in our understanding
of the likely occurrence of marine
mammal species in the vicinity of the
action, i.e., presence, abundance,
distribution, and/or density of species.
2. An increase in our understanding
of the nature, scope, or context of the
likely exposure of marine mammal
species to any of the potential stressor(s)
associated with the action (e.g. sound or
visual stimuli), through better
understanding of one or more of the
following: The action itself and its
environment (e.g. sound source
characterization, propagation, and
ambient noise levels); the affected
species (e.g. life history or dive pattern);
the likely co-occurrence of marine
mammal species with the action (in
whole or part) associated with specific
adverse effects; and/or the likely
biological or behavioral context of
exposure to the stressor for the marine
mammal (e.g. age class of exposed
animals or known pupping, calving or
feeding areas).
3. An increase in our understanding
of how individual marine mammals
respond (behaviorally or
physiologically) to the specific stressors
associated with the action (in specific
contexts, where possible, e.g., at what
distance or received level).
4. An increase in our understanding
of how anticipated individual
responses, to individual stressors or
anticipated combinations of stressors,
may impact either: The long-term fitness
and survival of an individual; or the
population, species, or stock (e.g.
through effects on annual rates of
recruitment or survival).
5. An increase in our understanding
of how the activity affects marine
mammal habitat, such as through effects
on prey sources or acoustic habitat (e.g.,
through characterization of longer-term
contributions of multiple sound sources
to rising ambient noise levels and
assessment of the potential chronic
effects on marine mammals).
6. An increase in understanding of the
impacts of the activity on marine
mammals in combination with the
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impacts of other anthropogenic
activities or natural factors occurring in
the region.
7. An increase in our understanding
of the effectiveness of mitigation and
monitoring measures.
8. An increase in the probability of
detecting marine mammals (through
improved technology or methodology),
both specifically within the safety zone
(thus allowing for more effective
implementation of the mitigation) and
in general, to better achieve the above
goals.
Proposed Monitoring Measures
1. Visual Monitoring
PSOs will be required to monitor the
area for marine mammals aboard the
drill rig during rig tow, exploratory
drilling operations, conductor pipe
driving, and VSP operations. Standard
marine mammal observing field
equipment will be used, including
reticule binoculars, Big-eye binoculars,
inclinometers, and range-finders. If
conductor pipe driving or VSP
operations occur at night, PSOs will be
equipped with night scopes. At least
one PSO will be on duty at all times
when operations are occurring. Shifts
shall not last more than 4 hours, and
PSOs will not observe for more than 12
hours in a 24-hour period.
2. Sound Source Verification
Monitoring
A sound source verification (SSV) of
the underwater sound pressures
emanating from the active drilling rig
will be conducted by an acoustical
engineer. The measurements would be
made in a boat that is drifting near the
rig in the current. Measuring while
drifting will minimize the noise
contamination caused by strumming of
the hydrophone lines and flow noise.
Measurements will be made with a twochannel system that will provide
measurements at two specified depths
up to 100 feet. The underwater sound
levels would be measured using
hydrophones, sound level meters, and
recording devices.
Measurements would be made by
hydrophones that have a flat frequency
response and are omnidirectional over a
frequency range of 10 to 20,000 Hz. The
signals shall be fed into an appropriate
date-logging device, such as an
integrating sound level meter. The
systems will have the capability to make
quality recordings using a digital audio
recorder (either solid state or tape). The
accuracy of the measurement system
shall be 1 dB from 10 to 10,000 Hz
referenced to 1 micro Pascal (mPa). The
measurement system shall be able to
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measure the unweighted or C-weighted
root-mean-square (rms) sound pressure
levels in dB referenced to 1 mPa. The
measurement systems will have the
capability to provide a real time readout
display of underwater sound levels. The
real-time display shall provide the
unweighted peak sound pressure and
the sound pressure level. During
drilling, measurements were made out
to beyond the 120 dB isopleth. During
any other activity (e.g., conductor
driving and VSP operations),
measurements were or will be made to
at least one kilometer from the rig. To
date, SSVs have been conducted for
drilling operations, generators,
submersed pumps, and VSP operations
(I&R, 2013a, b, c). SSV of the conductor
pipe driving activity is planned to
occur.
Recordings of sounds will be
conducted so that subsequent analysis
could be provided and certain sounds
could be identified or at least described.
The subsequent analysis would include
providing frequency spectra for different
sounds or distances from the rig. The
spectra data would be provided in 1⁄3rd
octave bands for sounds in the 10 to
10,000 Hz range.
In addition to the underwater sound
measurements, measurements of sea
temperature, wind speed, and sea state
will be (or were) taken as well.
Reporting Measures
1. SSV Report
The SSV report will describe the
source of the sound, the environment,
the measurements, and the methodology
employed to make the measurements.
Results will be presented as overall
sound pressure levels and displays of 1/
3rd octave band sound levels.
Preliminary findings relative to the 120
dB, 160 dB, 180 dB, and 190 dB
isopleths will be provided within 1
week of SSV completion.
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2. 90-Day Technical Report
Daily field reports will be prepared
that include daily activities, marine
mammal monitoring efforts, and a
record of the marine mammals and their
behaviors and reactions observed that
day. These daily reports will be used to
help generate the 90-day technical
report. A report will be due to NMFS no
later than 90 days after the expiration of
the IHA (if issued). The Technical
Report will include the following:
• Summaries of monitoring effort
(e.g., total hours, total distances, and
marine mammal distribution through
the study period, accounting for sea
state and other factors affecting
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visibility and detectability of marine
mammals).
• Analyses of the effects of various
factors influencing detectability of
marine mammals (e.g., sea state, number
of observers, and fog/glare).
• Species composition, occurrence,
and distribution of marine mammal
sightings, including date, water depth,
numbers, age/size/gender categories (if
determinable), group sizes, and ice
cover.
• Analyses of the effects of
operations.
• Sighting rates of marine mammals
(and other variables that could affect
detectability), such as: (i) Initial sighting
distances versus operational activity
state; (ii) closest point of approach
versus operational activity state; (iii)
observed behaviors and types of
movements versus operational activity
state; (iv) numbers of sightings/
individuals seen versus operational
activity state; (v) distribution around the
drill rig versus operational activity state;
and (vi) estimates of take by Level B
harassment based on presence in the
Level B harassment zones.
3. Notification of Injured or Dead
Marine Mammals
In the unanticipated event that the
specified activity clearly causes the take
of a marine mammal in a manner
prohibited by the IHA (if issued), such
as an injury (Level A harassment),
serious injury or mortality (e.g., shipstrike, gear interaction, and/or
entanglement), Buccaneer would
immediately cease the specified
activities and immediately report the
incident to the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, and the
Alaska Regional Stranding Coordinators.
The report would include the following
information:
• Time, date, and location (latitude/
longitude) of the incident;
• Name and type of vessel involved;
• Vessel’s speed during and leading
up to the incident;
• Description of the incident;
• Status of all sound source use in the
24 hours preceding the incident;
• Water depth;
• Environmental conditions (e.g.,
wind speed and direction, Beaufort sea
state, cloud cover, and visibility);
• Description of all marine mammal
observations in the 24 hours preceding
the incident;
• Species identification or
description of the animal(s) involved;
• Fate of the animal(s); and
• Photographs or video footage of the
animal(s) (if equipment is available).
Activities would not resume until
NMFS is able to review the
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circumstances of the prohibited take.
NMFS would work with Buccaneer to
determine what is necessary to
minimize the likelihood of further
prohibited take and ensure MMPA
compliance. Buccaneer would not be
able to resume their activities until
notified by NMFS via letter, email, or
telephone.
In the event that Buccaneer discovers
an injured or dead marine mammal, and
the lead PSO determines that the cause
of the injury or death is unknown and
the death is relatively recent (i.e., in less
than a moderate state of decomposition
as described in the next paragraph),
Buccaneer would immediately report
the incident to the Chief of the Permits
and Conservation Division, Office of
Protected Resources, NMFS, and the
NMFS Alaska Stranding Hotline and/or
by email to the Alaska Regional
Stranding Coordinators. The report
would include the same information
identified in the paragraph above.
Activities would be able to continue
while NMFS reviews the circumstances
of the incident. NMFS would work with
Buccaneer to determine whether
modifications in the activities are
appropriate.
In the event that Buccaneer discovers
an injured or dead marine mammal, and
the lead PSO determines that the injury
or death is not associated with or related
to the activities authorized in the IHA
(e.g., previously wounded animal,
carcass with moderate to advanced
decomposition, or scavenger damage),
Buccaneer would report the incident to
the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, and the
NMFS Alaska Stranding Hotline and/or
by email to the Alaska Regional
Stranding Coordinators, within 24 hours
of the discovery. Buccaneer would
provide photographs or video footage (if
available) or other documentation of the
stranded animal sighting to NMFS and
the Marine Mammal Stranding Network.
Estimated Take by Incidental
Harassment
Except with respect to certain
activities not pertinent here, the MMPA
defines ‘‘harassment’’ as: any act of
pursuit, torment, or annoyance which (i)
has the potential to injure a marine
mammal or marine mammal stock in the
wild [Level A harassment]; or (ii) has
the potential to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of behavioral
patterns, including, but not limited to,
migration, breathing, nursing, breeding,
feeding, or sheltering [Level B
harassment]. Only take by Level B
behavioral harassment of some species
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is anticipated as a result of the proposed
drilling program. Anticipated impacts to
marine mammals are associated with
noise propagation from the sound
sources (e.g., drill rig and tow, airguns,
and impact hammer) used in the drilling
program. Additional disturbance to
marine mammals may result from visual
disturbance of the drill rig or support
vessels. No take is expected to result
from vessel strikes because of the slow
speed of the vessels (2–4 knots while rig
is under two; 7–8 knots of supply
barges).
Buccaneer requests authorization to
take six marine mammal species by
Level B harassment. These six marine
mammal species are: Gray whale; minke
whale; killer whale; harbor porpoise;
Dall’s porpoise; and harbor seal. Take of
Cook Inlet beluga whales is not
requested, expected, or proposed to be
authorized. NMFS Section 7 ESA
biologists concluded that Buccaneer’s
proposed exploratory drilling program
is not likely to adversely affect Cook
Inlet beluga whales. Mitigation
measures requiring shutdowns of
activities before belugas enter the Level
B harassment zones will be required in
any issued IHA.
As noted previously in this document,
for continuous sounds, such as those
produced by drilling operations and rig
tow, NMFS uses a received level of 120dB (rms) to indicate the onset of Level
B harassment. For impulse sounds, such
as those produced by the airgun array
during the VSP surveys or the impact
hammer during conductor pipe driving,
NMFS uses a received level of 160-dB
(rms) to indicate the onset of Level B
harassment. The current Level A
(injury) harassment threshold is 180 dB
(rms) for cetaceans and 190 dB (rms) for
pinnipeds. Table 2 outlines the current
acoustic criteria.
TABLE 2—CURRENT ACOUSTIC EXPOSURE CRITERIA USED BY NMFS
Criterion
Criterion definition
Threshold
Level A Harassment (injury)
Permanent Threshold Shift (PTS) ...................................
(Any level above that which is known to cause TTS) ....
Behavioral Disruption ......................................................
(for impulse noises) .........................................................
Behavioral Disruption ......................................................
(for continuous, noise) ....................................................
180 dB re 1 microPa-m (cetaceans)/190 dB re 1
microPa-m (pinnipeds) root mean square (rms).
160 dB re 1 microPa-m (rms).
Level B Harassment ............
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Level B Harassment ............
120 dB re 1 microPa-m (rms).
Section 6 of Buccaneer’s application
contains a description of the
methodology used by Buccaneer to
estimate takes by harassment, including
calculations for the 120 dB (rms) and
160 dB (rms) isopleths and marine
mammal densities in the areas of
operation (see ADDRESSES), which is also
provided in the following sections.
NMFS verified Buccaneer’s methods,
and used the density and sound isopleth
measurements in estimating take.
However, NMFS also include a duration
factor in the estimates presented below,
which is not included in Buccaneer’s
application.
Simply, the proposed take estimates
presented in this section for harbor
porpoise and harbor seal were
calculated by multiplying summer
density for the species (which
constitutes the best available density
information) by the area of
ensonification for each type of activity
by the total number of days that each
activity would occur. For the other four
species (minke, gray, and killer whales
and Dall’s porpoise), there are no
available density estimates because of
their low occurrence rates in Cook Inlet.
Therefore, take requests for those
species are based on opportunistic
sightings data and typical group size for
each species. Additional detail is
provided next.
the longer tows will take 2 days to
complete. The rig will be wet-towed by
at least two ocean-going tugs licensed to
operate in Cook Inlet. Tugs generate
their loudest sounds while towing due
to propeller cavitation. While these
continuous sounds have been measured
at up to 171 dB re 1 mPa-m (rms) at
source (broadband), they are generally
emitted at dominant frequencies of less
than 5 kHz (Miles et al., 1987;
Richardson et al., 1995; Simmonds et
al., 2004).
For the most part, the dominant noise
frequencies from propeller cavitation
are less than the dominant hearing
frequencies for pinnipeds and toothed
whales. Because it is currently unknown
which tug or tugs will be used to tow
the rig, and there are few sound
signatures for tugs in general, the
potential area that could be ensonified
by disturbance-level noise is calculated
based on an assumed 171 dB re 1
mPa-m source. Using Collins et al.’s
(2007) 171—18.4 Log(R)—0.00188
spreading model determine from
hydroacoustic surveys in Cook Inlet, the
distance to the 120 dB isopleth would
be at 1,715 ft (523 m). The associated
ZOI (area ensonified by noise greater
than 120 dB) is, therefore, 212 acres
(0.86 km2).
Ensonified Areas
The Delmar D62–22 diesel impact
hammer proposed to be used by
Buccaneer to drive the 30-inch
conductor pipe was previously
acoustically measured by Blackwell
1. Rig Tow
The jack-up rig will be towed three
times during 2014. It is estimated that
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2. Conductor Pipe Driving
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(2005) in upper Cook Inlet. She found
that sound exceeding 190 dB Level A
noise limits for pinnipeds extend to
about 200 feet (60 meters), and 180 dB
Level A impacts to cetaceans to about
820 feet (250 meters). Level B
disturbance levels of 160 dB extended to
just less than 1.2 miles (1.9 kilometers).
The associated ZOI (area ensonified by
noise greater than 160 dB) is 4.4 mi2
(11.3 km2).
3. Deep-Well Pumps (Jack-Up Rig)
Buccaneer proposes to use the jack-up
drilling rig Endeavour for the Cook Inlet
program. Because the drilling platform
and other noise-generating equipment
on a jack-up rig are located above the
sea’s surface, and there is very little
surface contact with the water compared
to drill ships and semisubmersible drill
rigs, lattice-legged jack-up drill rigs are
relatively quiet (Richardson et al., 1995;
Spence et al., 2007).
The Spartan 151, the only other jackup drill rig currently operating in the
Cook Inlet, was hydroacoustically
measured by Marine Acoustics, Inc.
(2011) in 2011. The survey results
showed that continuous noise levels
exceeding 120 dB re 1 mPa extended out
only 50 m (164 ft), and that this noise
was largely associated with the diesel
engines used as hotel power generators,
rather than the drilling table. Similar, or
lesser, noise levels were expected to be
generated by the Endeavour because
generators are mounted on pedestals
specifically to reduce noise transfer
through the infrastructure, and enclosed
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in an insulated engine room, with the
intent of reducing underwater noise
transmission to levels even lower than
the Spartan 151. This was confirmed
during an SSV test on the Endeavour by
Illingworth and Rodkin (2013a) in May
2013 where it was determined that the
noise levels associated with drilling and
operating generators are below ambient.
However, the SSV identified another
sound source, the submersed deep-well
pumps, which were emitting
underwater noise exceeding 120 dB. In
the initial testing (I&R 2013a), the noise
from the pump and the associated
falling (from deck level) water discharge
was found to exceed 120 dB re 1 mPa out
a distance just beyond 984 ft (300 m).
After the falling water was piped as a
mitigation measure to reduce noise
levels, the pump noise was retested (I&R
2013b) with the results indicating that
the primary deep-well pump, operating
inside the bow leg, still exceeded 120
dB re 1 mPa at a maximum of 853 ft
(260 m). For calculating potential
incidental harassment take, the 853-ft
(260-m) distance to the 120 dB isopleth
will be used giving a ZOI of 52.5 acres
(0.21 km2).
4. VSP Airguns
Illingworth and Rodkin (2013c)
measured noise levels during VSP
operations associated with Buccaneer
post-drilling operations at the
Cosmopolitan # 1 site in lower Cook
Inlet during July 2013. The results
indicated that the 720 cubic inch airgun
array used during the operation
produced noise levels exceeding 160 dB
re 1 mPa out to a distance of
approximately 8,100 ft (2,470 m). Based
on these results, the associated ZOI
would be 7.4 mi2 (19.2 km2).
Marine Mammal Densities
Density estimates were derived for
harbor porpoises and harbor seals as
described next. Because of their low
numbers, there are no available Cook
Inlet density estimates for the other
marine mammals that occasionally
inhabit Cook Inlet north of Anchor
Point.
1. Harbor Porpoise
Hobbs and Waite (2010) calculated a
Cook Inlet harbor porpoise density
estimate of 0.013 per km2 based on
sightings recorded during a summer
1998 aerial survey targeting beluga
whales. They derived the value by
dividing estimated number of harbor
porpoise inhabiting Cook Inlet (249) by
the area of the entire inlet (18,948 km2).
2. Harbor Seal
Boveng et al. (2003) estimated the
harbor seal population that inhabits
Cook Inlet at 5,268 seals based on
summer/early fall surveys. Dividing that
value by the area of the inlet (18,948
km2) provides a Cook Inlet-wide density
of 0.278 seals per km2.
Proposed Take Estimates
As noted previously in this document,
the potential number of harbor
porpoises and harbor seals that might be
exposed to received continuous SPLs of
≥120 dB re 1 mPa (rms) and pulsed SPLs
of ≥160 dB re 1 mPa (rms) was calculated
by multiplying:
• The expected species density;
• the anticipated area to be ensonified
by the 120 dB re 1 mPa (rms) SPL (rig
tow and deep-well pumps) and 160 dB
re 1 mPa (rms) SPL (VSP airgun
operations and impact hammering); and
• the estimated total duration of each
of the activities expressed in days (24
hrs).
To derive at an estimated total
duration for each of the activities the
following assumptions were made:
• The total duration for rig tow over
the entire season would be 5 days.
• It is estimated to take between 30
and 75 days to drill one well. Assuming
the maximum time needed to drill a
well and that up to two wells may be
drilled under this IHA (if issued), the
total duration of deep-well pump usage
for two wells would be 150 days.
• The total duration of impact
hammering during conductor pipe
driving for two wells would be 6 days.
• The total duration of the two VSP
data acquisition runs is estimated to be
4 days.
Using all of these assumptions, Table
3 outlines the total number of Level B
harassment exposures for harbor seals
and harbor porpoises from each of the
four activities.
TABLE 3—POTENTIAL NUMBER OF EXPOSURES TO LEVEL B HARASSMENT THRESHOLDS DURING BUCCANEER’S PROPOSED
EXPLORATORY DRILLING PROGRAM DURING THE 2014 OPEN WATER SEASON
Species
Deep-well
pump
Rig tow
Harbor porpoise ...............................................................
Harbor Seal ......................................................................
For the less common marine
mammals such as gray, minke, killer
whales, and Dall’s porpoise, population
estimates within central and upper Cook
Inlet are too small to calculate density
estimates. Still, at even very low
densities, it is possible to encounter
these marine mammals during
0.05
1.2
Pipe driving
3
9
Buccaneer operations, especially during
towing operations through lower Cook
Inlet. Marine mammals may approach
the drilling rig out of curiosity, and
animals may approach in a group. Thus,
requested take authorizations for these
species are primarily based on group
size and the potential for attraction.
0.9
18.8
VSP
Total
1
21.4
Table 4 here outlines the density
estimates used to estimate Level B takes,
the proposed Level B harassment take
levels, the abundance of each species in
Cook Inlet, the percentage of each
species or stock estimated to be taken,
and current population trends.
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TABLE 4—DENSITY ESTIMATES, PROPOSED LEVEL B HARASSMENT TAKE LEVELS, SPECIES OR STOCK ABUNDANCE,
PERCENTAGE OF POPULATION PROPOSED TO BE TAKEN, AND SPECIES TREND STATUS
Species
Harbor Seal ...................
Harbor Porpoise ............
Killer Whale ...................
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Density
(# /km2)
Proposed
Level B take
0.278
0.013
NA
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51
5
5
PO 00000
Percentage of
population
Abundance
22,900 ...........................
25,987 ...........................
1,123 (resident) .............
552 (transient)
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5
51
0.22
0.02
0.45
0.91
E:\FR\FM\07APN2.SGM
Trend
Stable.
No reliable information.
Resident stock possibly increasing.
Transient stock stable.
07APN2
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TABLE 4—DENSITY ESTIMATES, PROPOSED LEVEL B HARASSMENT TAKE LEVELS, SPECIES OR STOCK ABUNDANCE,
PERCENTAGE OF POPULATION PROPOSED TO BE TAKEN, AND SPECIES TREND STATUS—Continued
Species
Gray whale ....................
Minke whale ..................
Dall’s porpoise ...............
Proposed
Level B take
Density
(# /km2)
NA
NA
NA
2
2
5
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Analysis and Preliminary
Determinations
Negligible Impact
Negligible impact is ‘‘an impact
resulting from the specified activity that
cannot be reasonably expected to, and is
not reasonably likely to, adversely affect
the species or stock through effects on
annual rates of recruitment or survival’’
(50 CFR 216.103). A negligible impact
finding is based on the lack of likely
adverse effects on annual rates of
recruitment or survival (i.e., populationlevel effects). An estimate of the number
of Level B harassment takes, alone, is
not enough information on which to
base an impact determination. In
addition to considering estimates of the
number of marine mammals that might
be ‘‘taken’’ through behavioral
harassment, NMFS must consider other
factors, such as the likely nature of any
responses (their intensity, duration,
etc.), the context of any responses
(critical reproductive time or location,
feeding, migration, etc.), as well as the
number and nature of estimated Level A
harassment takes, the number of
estimated mortalities, effects on habitat,
and the status of the species.
No injuries or mortalities are
anticipated to occur as a result of
Buccaneer’s proposed exploratory
drilling program, and none are proposed
to be authorized. Injury, serious injury,
or mortality could occur if there were a
large or very large oil spill. However, as
discussed previously in this document,
the likelihood of a spill is extremely
remote. Buccaneer has implemented
many design and operational standards
to mitigate the potential for an oil spill
of any size. NMFS does not propose to
authorize take from an oil spill, as it is
not part of the specified activity.
Additionally, animals in the area are not
expected to incur hearing impairment
(i.e., TTS or PTS) or non-auditory
physiological effects. Instead, any
impact that could result from
Buccaneer’s activities is most likely to
be behavioral harassment and is
expected to be of limited duration.
None of the species for which take is
proposed to be authorized are listed as
threatened or endangered under the
ESA nor as depleted under the MMPA.
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Percentage of
population
Abundance
18,017 ...........................
810–1,233 .....................
83,400 ...........................
Trend
0.01
0.16–0.25
0.01
Stable/increasing.
No reliable information.
No reliable information.
Additionally, no critical habitat exists
for these species. Buccaneer’s proposed
exploratory drilling program will occur
south of critical habitat designated as
priority Area 1 for Cook Inlet beluga
whales, but activities will occur in
habitat designated as priority Area 2.
During the proposed period of
operations, the majority of Cook Inlet
beluga whales will be in Area 1 critical
habitat, north of the proposed drilling
area. The proposed activities are not
anticipated to destroy or adversely
modify beluga whale critical habitat,
and mitigation measures and safety
protocols are in place to reduce any
potential even further.
Sound levels emitted during the
proposed program are anticipated to be
low. The continuous sounds produced
by the drill rig do not even rise to the
level thought to cause auditory injury in
marine mammals. Additionally, impact
hammering and airgun operations will
occur for extremely limited time periods
(for a few hours at a time for 1–3 days
per well and for a few hours at a time
for 1–2 days per well, respectively).
Moreover, auditory injury has not been
noted in marine mammals from these
activities either. Mitigation measures
proposed for inclusion in any issued
IHA will reduce these potentials even
further.
Potential impacts to marine mammal
habitat were discussed previously in
this document (see the ‘‘Anticipated
Effects on Habitat’’ section). Although
some disturbance is possible to food
sources of marine mammals, the
impacts are anticipated to be minor
enough as to not affect annual rates of
recruitment or survival of marine
mammals in the area. Based on the size
of Cook Inlet where feeding by marine
mammals occurs versus the localized
area of drilling program activities, any
missed feeding opportunities in the
direct project area would be minor
based on the fact that other feeding
areas exist elsewhere. Additionally,
drilling operations will not occur in the
primary beluga feeding and calving
habitat.
Taking into account the mitigation
measures that are planned, effects on
marine mammals are generally expected
to be restricted to avoidance of a limited
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area around the drilling operation and
short-term changes in behavior, falling
within the MMPA definition of ‘‘Level
B harassment’’. Animals are not
expected to permanently abandon any
area that is part of the drilling
operations, and any behaviors that are
interrupted during the activity are
expected to resume once the activity
ceases. Only a small portion of marine
mammal habitat will be affected at any
time, and other areas within Cook Inlet
will be available for necessary biological
functions. Based on the analysis
contained herein of the likely effects of
the specified activity on marine
mammals and their habitat, and taking
into consideration the implementation
of the proposed monitoring and
mitigation measures, NMFS
preliminarily finds that the total marine
mammal take from Buccaneer’s
proposed exploratory drilling program
will have a negligible impact on the
affected marine mammal species or
stocks.
Small Numbers
The requested takes proposed to be
authorized represent 0.45 percent of the
Alaska resident stock and 0.91 percent
of the Gulf of Alaska, Aleutian Island
and Bering Sea stock of killer whales
(1,123 residents and 552 transients),
0.02 percent of the Gulf of Alaska stock
of approximately 25,987 harbor
porpoises, 0.01 percent of the Alaska
stock of approximately 83,400 Dall’s
porpoises, 0.16–0.25 percent of the
Alaska stock of approximately 810–
1,233 minke whales, and 0.01 percent of
the eastern North Pacific stock of
approximately 18,017 gray whales. The
take request presented for harbor seals
represent 0.22 percent of the Cook Inlet/
Shelikof stock of approximately 29,175
animals. These take estimates represent
the percentage of each species or stock
that could be taken by Level B
behavioral harassment if each animal is
taken only once. The numbers of marine
mammals taken are small relative to the
affected species or stock sizes. In
addition, the mitigation and monitoring
measures (described previously in this
document) proposed for inclusion in the
IHA (if issued) are expected to reduce
even further any potential disturbance
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to marine mammals. NMFS
preliminarily finds that small numbers
of marine mammals will be taken
relative to the populations of the
affected species or stocks.
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Impact on Availability of Affected
Species for Taking for Subsistence Uses
Relevant Subsistence Uses
The subsistence harvest of marine
mammals transcends the nutritional and
economic values attributed to the
animal and is an integral part of the
cultural identity of the region’s Alaska
Native communities. Inedible parts of
the whale provide Native artisans with
materials for cultural handicrafts, and
the hunting itself perpetuates Native
traditions by transmitting traditional
skills and knowledge to younger
generations (NOAA, 2007).
The Cook Inlet beluga whale has
traditionally been hunted by Alaska
Natives for subsistence purposes. For
several decades prior to the 1980s, the
Native Village of Tyonek residents were
the primary subsistence hunters of Cook
Inlet beluga whales. During the 1980s
and 1990s, Alaska Natives from villages
in the western, northwestern, and North
Slope regions of Alaska either moved to
or visited the south central region and
participated in the yearly subsistence
harvest (Stanek, 1994). From 1994 to
1998, NMFS estimated 65 whales per
year (range 21–123) were taken in this
harvest, including those successfully
taken for food and those struck and lost.
NMFS has concluded that this number
is high enough to account for the
estimated 14 percent annual decline in
the population during this time (Hobbs
et al., 2008). Actual mortality may have
been higher, given the difficulty of
estimating the number of whales struck
and lost during the hunts. In 1999, a
moratorium was enacted (Public Law
106–31) prohibiting the subsistence take
of Cook Inlet beluga whales except
through a cooperative agreement
between NMFS and the affected Alaska
Native organizations. Since the Cook
Inlet beluga whale harvest was regulated
in 1999 requiring cooperative
agreements, five beluga whales have
been struck and harvested. Those beluga
whales were harvested in 2001 (one
animal), 2002 (one animal), 2003 (one
animal), and 2005 (two animals). The
Native Village of Tyonek agreed not to
hunt or request a hunt in 2007, when no
co-management agreement was to be
signed (NMFS, 2008a).
On October 15, 2008, NMFS
published a final rule that established
long-term harvest limits on the Cook
Inlet beluga whales that may be taken by
Alaska Natives for subsistence purposes
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(73 FR 60976). That rule prohibits
harvest for a 5-year period (2008–2012),
if the average abundance for the Cook
Inlet beluga whales from the prior five
years (2003–2007) is below 350 whales.
The next 5-year period that could allow
for a harvest (2013–2017), would require
the previous five-year average (2008–
2012) to be above 350 whales. The 2008
Cook Inlet Beluga Whale Subsistence
Harvest Final Supplemental
Environmental Impact Statement
(NMFS, 2008a) authorizes how many
beluga whales can be taken during a 5year interval based on the 5-year
population estimates and 10-year
measure of the population growth rate.
Based on the 2008–2012 5-year
abundance estimates, no hunt occurred
between 2008 and 2012 (NMFS, 2008a).
The Cook Inlet Marine Mammal
Council, which managed the Alaska
Native Subsistence fishery with NMFS,
was disbanded by a unanimous vote of
the Tribes’ representatives on June 20,
2012. At this time, no harvest is
expected in 2013 or 2014. Residents of
the Native Village of Tyonek are the
primary subsistence users in Knik Arm
area.
Data on the harvest of other marine
mammals in Cook Inlet are lacking.
Some data are available on the
subsistence harvest of harbor seals,
harbor porpoises, and killer whales in
Alaska in the marine mammal stock
assessments. However, these numbers
are for the Gulf of Alaska including
Cook Inlet, and they are not indicative
of the harvest in Cook Inlet.
Some detailed information on the
subsistence harvest of harbor seals is
available from past studies conducted
by the Alaska Department of Fish &
Game (Wolfe et al., 2009). In 2008, only
33 harbor seals were taken for harvest in
the Upper Kenai-Cook Inlet area. In the
same study, reports from hunters stated
that harbor seal populations in the area
were increasing (28.6%) or remaining
stable (71.4%). The specific hunting
regions identified were Anchorage,
Homer, Kenai, and Tyonek, and hunting
generally peaks in March, September,
and November (Wolfe et al., 2009).
Potential Impacts to Subsistence Uses
Section 101(a)(5)(D) also requires
NMFS to determine that the
authorization will not have an
unmitigable adverse effect on the
availability of marine mammal species
or stocks for subsistence use. NMFS has
defined ‘‘unmitigable adverse impact’’
in 50 CFR 216.103 as: An impact
resulting from the specified activity: (1)
That is likely to reduce the availability
of the species to a level insufficient for
a harvest to meet subsistence needs by:
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19277
(i) Causing the marine mammals to
abandon or avoid hunting areas; (ii)
Directly displacing subsistence users; or
(iii) Placing physical barriers between
the marine mammals and the
subsistence hunters; and (2) That cannot
be sufficiently mitigated by other
measures to increase the availability of
marine mammals to allow subsistence
needs to be met.
The primary concern is the
disturbance of marine mammals through
the introduction of anthropogenic sound
into the marine environment during the
proposed exploratory drilling operation.
Marine mammals could be behaviorally
harassed and either become more
difficult to hunt or temporarily abandon
traditional hunting grounds. If a large or
very large oil spill occurred, it could
impact subsistence species. However, as
previously mentioned one is not
anticipated to occur, and measures have
been taken to prevent a large or very
large oil spill. The proposed exploratory
drilling program should not have any
impacts to beluga harvests as none
currently occur in Cook Inlet, and no
takes of belugas are anticipated or
proposed to be authorized.
Additionally, subsistence harvests of
other marine mammal species are
limited in Cook Inlet.
Plan of Cooperation or Measures To
Minimize Impacts to Subsistence Hunts
Regulations at 50 CFR 216.104(a)(12)
require IHA applicants for activities that
take place in Arctic waters to provide a
Plan of Cooperation or information that
identifies what measures have been
taken and/or will be taken to minimize
adverse effects on the availability of
marine mammals for subsistence
purposes. NMFS regulations define
Arctic waters as waters above 60° N.
latitude. The proposed mitigation
measures described earlier in this
document will reduce impacts to any
hunts of harbor seals or other marine
mammal species that may occur in Cook
Inlet. These measures will ensure that
marine mammals are available to
subsistence hunters.
Unmitigable Adverse Impact Analysis
and Preliminary Determination
The project will not have any effect
on current beluga whale harvests
because no beluga harvest will take
place in 2014. Moreover, no take of
belugas is anticipated or proposed to be
authorized. Additionally, the proposed
drilling area is not an important native
subsistence site for other subsistence
species of marine mammals. Also,
because of the relatively small
proportion of marine mammals utilizing
Cook Inlet, the number harvested is
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expected to be extremely low.
Therefore, because the proposed
program would result in only temporary
disturbances, the drilling program
would not impact the availability of
these other marine mammal species for
subsistence uses.
The timing and location of
subsistence harvest of Cook Inlet harbor
seals may coincide with Buccaneer’s
project, but because this subsistence
hunt is conducted opportunistically and
at such a low level (NMFS, 2013c),
Buccaneer’s program is not expected to
have an impact on the subsistence use
of harbor seals. Moreover, hunts are
unlikely to occur in mid-channel waters
of Cook Inlet where drilling associated
activities would occur.
NMFS anticipates that any effects
from Buccaneer’s proposed exploratory
drilling program on marine mammals,
especially harbor seals and Cook Inlet
beluga whales, which are or have been
taken for subsistence uses, would be
short-term, site specific, and limited to
inconsequential changes in behavior.
NMFS does not anticipate that the
authorized taking of affected species or
stocks will reduce the availability of the
species to a level insufficient for a
harvest to meet subsistence needs by: (1)
Causing the marine mammals to
abandon or avoid hunting areas; (2)
directly displacing subsistence users; or
(3) placing physical barriers between the
marine mammals and the subsistence
hunters; and that cannot be sufficiently
mitigated by other measures to increase
the availability of marine mammals to
allow subsistence needs to be met. In
the unlikely event of a major oil spill in
Cook Inlet, there could be major impacts
on the availability of marine mammals
for subsistence uses. As discussed
earlier in this document, the probability
of a major oil spill occurring over the
life of the project is low. Additionally,
Buccaneer developed an ODPCP, which
was reviewed by NMFS and approved
by ADEC on August 29, 2012. Based on
the description of the specified activity,
the measures described to minimize
adverse effects on the availability of
marine mammals for subsistence
purposes, and the proposed mitigation
and monitoring measures, NMFS has
preliminarily determined that there will
not be an unmitgable adverse impact on
marine mammal availability for
subsistence uses from take incidental to
Buccaneer’s proposed activities.
Endangered Species Act (ESA)
Cook Inlet beluga whales are listed as
endangered under the ESA. The U.S.
Army Corps of Engineers consulted with
NMFS on this proposed project
pursuant to Section 7 of the ESA. On
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March 23, 2012, NMFS concluded that
the proposed exploratory drilling
program in upper Cook Inlet is not
likely to adversely affect beluga whales
or their critical habitat. On May 9, 2013,
NMFS received a letter requesting
reinitiation of consultation for
Buccaneer’s proposed operations due to
modifications to the project plan of
operations. On July 8, 2013, NMFS
again concluded that Buccaneer’s
proposed exploratory drilling program
in upper Cook Inlet is not likely to
adversely affect beluga whales or their
designated critical habitat. Mitigation
measures laid out in the Section 7
Letters of Concurrence to ensure no take
of beluga whales have been proposed for
inclusion in any issued IHA. Therefore,
NMFS’ Office of Protected Resources
does not intend to initiate formal
consultation under Section 7 of the
ESA.
National Environmental Policy Act
(NEPA)
NMFS is currently conducting an
analysis, pursuant to NEPA, to
determine whether this proposed IHA
may have a significant effect on the
human environment. This analysis will
be completed prior to the issuance or
denial of this proposed IHA.
Proposed Authorization
As a result of these preliminary
determinations, NMFS proposes to issue
an IHA to Buccaneer for conducting an
exploratory drilling program in upper
Cook Inlet during the 2014 open water
season, provided the previously
mentioned mitigation, monitoring, and
reporting requirements are incorporated.
The proposed IHA language is provided
next.
This section contains a draft of the
IHA itself. The wording contained in
this section is proposed for inclusion in
the IHA (if issued).
1. This IHA is valid from date of
issuance through October 31, 2014.
2. This IHA is valid only for activities
associated with Buccaneer’s upper Cook
Inlet exploratory drilling program. The
specific areas where Buccaneer’s
exploratory drilling operations will
occur are described in the August 2013
IHA application and depicted in Figure
1 of the application.
3. Species Authorized and Level of
Take
a. The incidental taking of marine
mammals, by Level B harassment only,
is limited to the following species in the
waters of Cook Inlet:
i. Odontocetes: 5 harbor porpoise; 5
Dall’s porpoise; and 5 killer whales.
ii. Mysticetes: 2 gray whales and 2
minke whales.
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iii. Pinnipeds: 51 harbor seals.
iv. If any marine mammal species not
listed in conditions 3(a)(i) through (iii)
are encountered during exploratory
drilling operations and are likely to be
exposed to sound pressure levels (SPLs)
greater than or equal to 160 dB re 1 m Pa
(rms) for impulse sources or greater than
or equal to 120 dB re 1 m Pa (rms), then
the Holder of this IHA must shut-down
the sound source to avoid take.
b. The taking by injury (Level A
harassment) serious injury, or death of
any of the species listed in condition
3(a) or the taking of any kind of any
other species of marine mammal is
prohibited and may result in the
modification, suspension or revocation
of this IHA.
4. The authorization for taking by
harassment is limited to the following
acoustic sources (or sources with
comparable frequency and intensity)
and from the following activities:
a. airgun array with a total discharge
volume of 720 in3;
b. continuous drill rig sounds during
active drilling operations and from rig
tow; and
c. impact hammer during conductor
pipe driving.
5. The taking of any marine mammal
in a manner prohibited under this
Authorization must be reported
immediately to the Chief, Permits and
Conservation Division, Office of
Protected Resources, NMFS or her
designee.
6. The holder of this IHA must notify
the Chief of the Permits and
Conservation Division, Office of
Protected Resources, at least 48 hours
prior to the start of exploration drilling
activities (unless constrained by the
date of issuance of this Authorization in
which case notification shall be made as
soon as possible).
7. Mitigation and Monitoring
Requirements: The Holder of this
Authorization is required to implement
the following mitigation and monitoring
requirements when conducting the
specified activities to achieve the least
practicable impact on affected marine
mammal species or stocks:
a. Utilize a sufficient number of
NMFS-qualified, vessel-based Protected
Species Observers (PSOs) to visually
watch for and monitor marine mammals
near the drill rig during daytime
operations (from nautical twilight-dawn
to nautical twilight-dusk) and before
and during start-ups of sound sources
day or night. PSOs shall have access to
reticle binoculars, big-eye binoculars,
and night vision devices. PSO shifts
shall last no longer than 4 hours at a
time. PSOs shall also make observations
during daytime periods when the sound
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sources are not operating for
comparison of animal abundance and
behavior, when feasible. When
practicable, as an additional means of
visual observation, drill rig or vessel
crew may also assist in detecting marine
mammals.
b. When a mammal sighting is made,
the following information about the
sighting will be recorded:
i. Species, group size, age/size/sex
categories (if determinable), behavior
when first sighted and after initial
sighting, heading (if consistent), bearing
and distance from the PSO, apparent
reaction to activities (e.g., none,
avoidance, approach, paralleling, etc.),
closest point of approach, and
behavioral pace;
ii. Time, location, speed, activity of
the vessel, sea state, ice cover, visibility,
and sun glare;
iii. The positions of other vessel(s) in
the vicinity of the PSO location (if
applicable);
iv. The rig’s position, speed if under
tow, and water depth, sea state, ice
cover, visibility, and sun glare will also
be recorded at the start and end of each
observation watch, every 30 minutes
during a watch, and whenever there is
a change in any of those variables.
c. Within safe limits, the PSOs should
be stationed where they have the best
possible viewing;
d. PSOs should be instructed to
identify animals as unknown where
appropriate rather than strive to identify
a species if there is significant
uncertainty;
e. Conductor Pipe Driving Mitigation
Measures:
i. PSOs will observe from the drill rig
during impact hammering out to the 160
dB (rms) radius of 2 km (1.24 mi). If
marine mammal species for which take
is not authorized enter this zone, then
use of the impact hammer will cease.
ii. If cetaceans for which take is
authorized enter within the 180 dB
(rms) radius of 250 m (820 ft) or if
pinnipeds for which take is authorized
enter within the 190 dB (rms) radius of
60 m (200 ft), then use of the impact
hammer will cease. Following a
shutdown of impact hammering
activities, the applicable zones must be
clear of marine mammals for at least 30
minutes prior to restarting activities.
iii. PSOs will visually monitor out to
the 160 dB radius for at least 30 minutes
prior to the initiation of activities. If no
marine mammals are detected during
that time, then Buccaneer can initiate
impact hammering using a ‘‘soft start’’
technique. Hammering will begin with
an initial set of three strikes at 40
percent energy followed by a 1 min
waiting period, then two subsequent
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three-strike sets. This ‘‘soft-start’’
procedure will be implemented anytime
impact hammering has ceased for 30
minutes or more. Impact hammer ‘‘softstart’’ will not be required if the
hammering downtime is for less than 30
minutes and visuals surveys are
continued throughout the silent period
and no marine mammals are observed in
the applicable zones during that time.
f. VSP Airgun Mitigation Measures:
i. PSOs will observe from the drill rig
during airgun operations out to the 160
dB radius of 2.5 km (1.55 mi). If marine
mammal species for which take is not
authorized enter this zone, then use of
the airguns will cease.
ii. If cetaceans for which take is
authorized enter within the 180 dB
(rms) radius of 240 m (787 ft) or if
pinnipeds for which take is authorized
enter within the 190 dB (rms) radius of
75 m (246 ft), then use of the airguns
will cease. Following a shutdown of
airgun operations, the applicable zones
must be clear of marine mammals for at
least 30 minutes prior to restarting
activities.
iii. PSOs will visually monitor out to
the 160 dB radius for at least 30 minutes
prior to the initiation of activities. If no
marine mammals are detected during
that time, then Buccaneer can initiate
airgun operations using a ‘‘ramp-up’’
technique. Airgun operations will begin
with the firing of a single airgun, which
will be the smallest gun in the array in
terms of energy output (dB) and volume
(in3). Operators will then continue
ramp-up by gradually activating
additional airguns over a period of at
least 30 minutes (but not longer than 40
minutes) until the desired operating
level of the airgun array is obtained.
This ramp-up procedure will be
implemented anytime airguns have not
been fired for 30 minutes or more.
Airgun ramp-up will not be required if
the airguns have been off for less than
30 minutes and visuals surveys are
continued throughout the silent period
and no marine mammals are observed in
the applicable zones during that time.
g. No initiation of survey operations
involving the use of sound sources is
permitted from a shutdown position at
night or during low-light hours (such as
in dense fog or heavy rain).
h. Field Source Verification: The
Holder of this IHA is required to
conduct sound source verification tests
for the drill rig, impact hammer, and the
airgun array. Sound source verification
shall consist of distances where
broadside and endfire directions at
which broadband received levels reach
190, 180, 170, 160, and 120 dB re 1 m Pa
(rms) for all active acoustic sources that
may be used during the activities. Initial
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results must be provided to NMFS
within 1 week of completing the
analysis.
i. Helicopters must maintain an
altitude of at least 1,000 ft (305 m),
except during takeoffs, landings, or
emergency situations.
8. Reporting Requirements: The
Holder of this IHA is required to:
a. Submit an SSV report that describes
the source of the sound, the
environment, the measurements, and
the methodology employed to make the
measurements. Results will be
presented as overall sound pressure
levels and displays of 1/3rd octave band
sound levels. Preliminary findings
relative to the 120 dB, 160 dB, 180 dB,
and 190 dB isopleths will be provided
within 1 week of SSV completion.
b. Submit a draft Technical Report on
all activities and monitoring results to
NMFS’ Permits and Conservation
Division within 90 days of expiration of
the IHA. The Technical Report will
include:
i. Summaries of monitoring effort
(e.g., total hours, total distances, and
marine mammal distribution through
the study period, accounting for sea
state and other factors affecting
visibility and detectability of marine
mammals);
ii. Analyses of the effects of various
factors influencing detectability of
marine mammals (e.g., sea state, number
of observers, and fog/glare);
iii. Species composition, occurrence,
and distribution of marine mammal
sightings, including date, water depth,
numbers, age/size/gender categories (if
determinable), group sizes, and ice
cover;
iv. Analyses of the effects of drilling
operation activities;
v. Sighting rates of marine mammals
during periods with and without
drilling operation activities (and other
variables that could affect detectability),
such as: (A) Initial sighting distances
versus activity state; (B) closest point of
approach versus activity state; (C)
observed behaviors and types of
movements versus activity state; (D)
numbers of sightings/individuals seen
versus activity state; (E) distribution
around the drill rig versus activity state;
and (F) estimates of take by Level B
harassment based on presence in the
120 dB and 160 dB harassment zones.
c. Submit a final report to the Chief,
Permits and Conservation Division,
Office of Protected Resources, NMFS,
within 30 days after receiving comments
from NMFS on the draft technical
report. If NMFS has no comments on the
draft technical report, the draft report
shall be considered to be the final
report.
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9. a. In the unanticipated event that
the specified activity clearly causes the
take of a marine mammal in a manner
prohibited by this IHA, such as an
injury (Level A harassment), serious
injury or mortality (e.g., ship-strike, gear
interaction, and/or entanglement),
Buccaneer shall immediately cease the
specified activities and immediately
report the incident to the Chief of the
Permits and Conservation Division,
Office of Protected Resources, NMFS,
her designees, and the Alaska Regional
Stranding Coordinators. The report must
include the following information:
i. Time, date, and location (latitude/
longitude) of the incident;
ii. The name and type of vessel
involved;
iii. The vessel’s speed during and
leading up to the incident;
iv. Description of the incident;
v. Status of all sound source use in
the 24 hours preceding the incident;
vi. Water depth;
vii. Environmental conditions (e.g.,
wind speed and direction, Beaufort sea
state, cloud cover, and visibility);
viii. Description of marine mammal
observations in the 24 hours preceding
the incident;
ix. Species identification or
description of the animal(s) involved;
x. The fate of the animal(s); and
xi. Photographs or video footage of the
animal (if equipment is available).
Activities shall not resume until
NMFS is able to review the
circumstances of the prohibited take.
NMFS shall work with Buccaneer to
determine what is necessary to
minimize the likelihood of further
prohibited take and ensure MMPA
compliance. Buccaneer may not resume
their activities until notified by NMFS
via letter or email, or telephone.
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b. In the event that Buccaneer
discovers an injured or dead marine
mammal, and the lead PSO determines
that the cause of the injury or death is
unknown and the death is relatively
recent (i.e., in less than a moderate state
of decomposition as described in the
next paragraph), Buccaneer will
immediately report the incident to the
Chief of the Permits and Conservation
Division, Office of Protected Resources,
NMFS, her designees, and the NMFS
Alaska Stranding Hotline. The report
must include the same information
identified in the Condition 9(a) above.
Activities may continue while NMFS
reviews the circumstances of the
incident. NMFS will work with Apache
to determine whether modifications in
the activities are appropriate.
c. In the event that Buccaneer
discovers an injured or dead marine
mammal, and the lead PSO determines
that the injury or death is not associated
with or related to the activities
authorized in Condition 2 of this
Authorization (e.g., previously wounded
animal, carcass with moderate to
advanced decomposition, or scavenger
damage), Buccaneer shall report the
incident to the Chief of the Permits and
Conservation Division, Office of
Protected Resources, NMFS, her
designees, the NMFS Alaska Stranding
Hotline (1–877–925–7773), and the
Alaska Regional Stranding Coordinators
within 24 hours of the discovery.
Buccaneer shall provide photographs or
video footage (if available) or other
documentation of the stranded animal
sighting to NMFS and the Marine
Mammal Stranding Network. Activities
may continue while NMFS reviews the
circumstances of the incident.
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10. Activities related to the
monitoring described in this IHA do not
require a separate scientific research
permit issued under section 104 of the
MMPA.
11. A copy of this Authorization must
be in the possession of all contractors
and PSOs operating under the authority
of this IHA.
12. Penalties and Permit Sanctions:
Any person who violates any provision
of this IHA is subject to civil and
criminal penalties, permit sanctions,
and forfeiture as authorized under the
MMPA.
13. This IHA may be modified,
suspended or withdrawn if the Holder
fails to abide by the conditions
prescribed herein or if the authorized
taking is having more than a negligible
impact on the species or stock of
affected marine mammals, or if there is
an unmitigable adverse impact on the
availability of such species or stocks for
subsistence uses.
Request for Public Comments
NMFS requests comment on our
analysis, the draft authorization, and
any other aspect of the Notice of
Proposed IHA for Buccaneer’s proposed
upper Cook Inlet exploratory drilling
program. Please include with your
comments any supporting data or
literature citations to help inform our
final decision on Buccaneer’s request for
an MMPA authorization.
Dated: March 31, 2014.
Perry F. Gayaldo,
Acting Deputy Director, Office of Protected
Resources, National Marine Fisheries Service.
[FR Doc. 2014–07601 Filed 4–4–14; 8:45 am]
BILLING CODE 3510–22–P
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[Federal Register Volume 79, Number 66 (Monday, April 7, 2014)]
[Notices]
[Pages 19251-19280]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-07601]
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Vol. 79
Monday,
No. 66
April 7, 2014
Part III
Department of Commerce
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National Oceanic and Atmospheric Administration
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Takes of Marine Mammals Incidental to Specified Activities; Taking
Marine Mammals Incidental to Buccaneer Energy Drilling Activities in
Upper Cook Inlet, 2014; Notice
Federal Register / Vol. 79 , No. 66 / Monday, April 7, 2014 /
Notices
[[Page 19252]]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XD165
Takes of Marine Mammals Incidental to Specified Activities;
Taking Marine Mammals Incidental to Buccaneer Energy Drilling
Activities in Upper Cook Inlet, 2014
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental harassment authorization; request
for comments.
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SUMMARY: NMFS has received an application from Buccaneer Alaska
Operation, LLC (Buccaneer) for an Incidental Harassment Authorization
(IHA) to take marine mammals, by harassment, incidental to conducting a
multi-well offshore exploratory drilling program in upper Cook Inlet
during the 2014 open water season. Pursuant to the Marine Mammal
Protection Act (MMPA), NMFS is requesting comments on its proposal to
issue an IHA to Buccaneer to incidentally take, by Level B harassment
only, marine mammals during the specified activity.
DATES: Comments and information must be received no later than May 7,
2014.
ADDRESSES: Comments on the application should be addressed to Jolie
Harrison, Supervisor, Incidental Take Program, Permits and Conservation
Division, Office of Protected Resources, National Marine Fisheries
Service, 1315 East-West Highway, Silver Spring, MD 20910. The mailbox
address for providing email comments is ITP.Nachman@noaa.gov. NMFS is
not responsible for email comments sent to addresses other than the one
provided here. Comments sent via email, including all attachments, must
not exceed a 25-megabyte file size.
Instructions: All comments received are a part of the public record
and will generally be posted to https://www.nmfs.noaa.gov/pr/permits/incidental.htm without change. All Personal Identifying Information
(e.g., name, address) voluntarily submitted by the commenter may be
publicly accessible. Do not submit Confidential Business Information or
otherwise sensitive or protected information.
An electronic 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. Documents cited in this
notice may also be viewed, by appointment, during regular business
hours, at the aforementioned address.
FOR FURTHER INFORMATION CONTACT: Candace Nachman, Office of Protected
Resources, NMFS, (301) 427-8401.
SUPPLEMENTARY INFORMATION:
Background
Sections 101(a)(5)(A) and (D) of the MMPA (16 U.S.C. 1361 et seq.)
direct the Secretary of Commerce to allow, upon request, the
incidental, but not intentional, taking of small numbers 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 for incidental takings shall be granted if NMFS finds
that the taking will have a negligible impact on the species or
stock(s), will not have an unmitigable adverse impact on the
availability of the species or stock(s) for subsistence uses (where
relevant), and if the permissible methods of taking, other means of
effecting the least practicable impact on the species or stock and its
habitat, 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.''
Except with respect to certain activities not pertinent here, the
MMPA defines ``harassment'' as: ``Any act of pursuit, torment, or
annoyance which (i) has the potential to injure a marine mammal or
marine mammal stock in the wild [Level A harassment]; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment].''
Summary of Request
On August 30, 2013, NMFS received an IHA application from Buccaneer
for the taking of marine mammals incidental to a multi-well, multi-year
offshore exploratory drilling program in upper Cook Inlet during the
2014 open water season (typically mid-April through October). This
request was for 1-year of the program. NMFS determined that the
application was adequate and complete on November 25, 2013. However, on
February 13, 2014, Buccaneer informed NMFS that a portion of the
activity contained in the application is no longer proposed. As
described in more detail below, Buccaneer proposes to drill four wells
instead of six during this multi-year program.
Buccaneer proposes to drill up to four exploratory wells during
this multi-year program and will likely drill up to two wells each year
at locations in upper Cook Inlet. The proposed activity for this IHA
(if issued) would occur during the open water months in 2014, which is
typically from April through October. The following specific aspects of
the proposed activities are likely to result in the take of marine
mammals: Driving of the conductor pipe; exploratory drilling; towing of
the jack-up drill rig; and vertical seismic profiling (VSP). Take, by
Level B harassment only, of six marine mammal species is anticipated to
result from the specified activity.
Description of the Specified Activity
Overview
Buccaneer proposes to conduct exploratory drilling operations at
multiple well sites in upper Cook Inlet during the 2014 summer and fall
open water (ice-free) season, using the Endeavour-Spirit of
Independence (Endeavour) jack-up drill rig. The rig will be towed
between drilling locations and winter moorage by ocean-going tugs. The
activities of relevance to this IHA request include: Mobilization and
demobilization of the drill rig to and from the well locations at the
start and end of the season; driving of the conductor pipe; exploratory
drilling; and VSP seismic operations. Buccaneer proposes to utilize
both helicopters and vessels to conduct resupply, crew change, and
other logistics during the exploratory drilling program.
Dates and Duration
The 2014 exploratory drilling program (which is the subject of this
IHA request) would occur during the 2014 open water season (April 15
through October 31). Drilling will take approximately 30 to 75 days per
well, and well testing will take another 7 to 15 days per well.
Buccaneer proposes to drill at up to two well locations in 2014 in
upper Cook Inlet. During this time period, conductor pipe driving would
only occur for a period of 1 to 3 days
[[Page 19253]]
at each location, and VSP seismic operations would only occur for a
period of less than 1 to 2 days at each location. The rig tows will
take approximately 2 days to complete during mobilization and
demobilization from upper Cook Inlet, and the shorter tow between the
two well locations in upper Cook Inlet will take a few hours. This IHA
(if issued) would be effective from date of issuance through October
31, 2014.
Specified Geographic Region
Buccaneer's proposed program would occur at up to two of four
possible well locations in upper Cook Inlet. The Tyonek Deep well sites
are the priority for the 2014 season. However, we are analyzing that
activity could occur at either Tyonek Deep 1, Tyonek Deep
2, Southern Cross 1, or Southern Cross 2 to
allow for operational flexibility. Figure 1 in Buccaneer's IHA
application depicts the location of these four well sites. All of these
wells are located in State of Alaska oil and gas leases in Cook Inlet.
Detailed Description of Activities
1. Drill Rig Mobilization and Towing
Buccaneer proposes to conduct the exploratory drilling program
using the Endeavour, which is an independent leg, cantilevered jack-up
drill rig of the Marathon LeTourneau Class 116-C and is capable of
drilling up to 25,000 ft in water depths from 15-300 ft. Additional
specifications can be found in Appendix A of the IHA application. The
rig will be towed between drilling locations and winter moorage by
ocean-going tugs licensed to operate in Cook Inlet. While under tow,
the rig operations will be monitored by Buccaneer and the drilling
contractor management, both aboard the rig and onshore.
The jack-up rig would be towed up to three times during the summer
and fall seasons of 2014. It is estimated that the longer tows will
take 2 days to complete, while the shorter tows between the upper Cook
Inlet wells will take but a few hours (distance between the two wells
is less than 5 miles).
The rig will be wet-towed by two or three ocean-going tugs licensed
to operate in the Cook Inlet. Tugs generate their loudest sounds while
towing due to propeller cavitation. While these continuous sounds have
been measured at up to 171 dB re 1 [mu]Pa-m (rms) at 1-meter source
(broadband), they are generally emitted at dominant frequencies of less
than 5 kHz (Miles et al., 1987; Richardson et al., 1995, Simmonds et
al., 2004). The distance to the 120-dB isopleth, assuming a 171 dB
source, is 1,715 feet (523 meters) using Collins et al.'s (2007) 171-
18.4 Log(R)--0.00188 R spreading model developed from Cook Inlet. For
the most part, the dominant noise frequencies from propeller cavitation
are significantly lower than the dominant hearing frequencies for
pinnipeds and toothed whales, including beluga whales (Wartzok and
Ketten, 1999).
2. Conductor Pipe Driving
A conductor pipe is a relatively short, large-diameter pipe driven
into the sediment prior to the drilling of oil wells. This section of
tubing serves to support the initial sedimentary part of the well,
preventing the looser surface layer from collapsing and obstructing the
wellbore. The pipe also facilitates the return of cuttings from the
drill head. Conductor pipes are usually installed using drilling, pile
driving, or a combination of these techniques. In offshore wells, the
conductor pipe is also used as a foundation for the wellhead. Buccaneer
proposes to drive approximately 300 ft (90 m) of 30-inch conductor pipe
at each of the upper Cook Inlet wells prior to drilling using a Delmar
D62-22 impact hammer. This hammer has impact weight of 13,640 pounds
(6,200 kg) and reaches a maximum impact energy of 165,215 foot-pounds
(224 kilonewton-meters) at a drop height of 12 feet (3.6 meters).
Blackwell (2005) measured the noise produced by a Delmar D62-22
driving 36-inch steel pipe in upper Cook Inlet and found sound pressure
levels to exceed 190 dB re 1[mu]Pa-m (rms) at about 200 ft (60 m), 180
dB re 1[mu]Pa-m (rms) at about 820 ft (250 m), and 160 dB re 1[mu]Pa-m
(rms) at just less than 1.2 mi (1.9 km). Each conductor pipe driving
event is expected to last 1 to 3 days, although actual sound generation
(pounding) would occur only intermittently during this period.
3. Exploratory Drilling and Standard Operation
The jack-up drilling rig Endeavour's drilling platform and other
noise-generating equipment is located above the sea's surface, and
there is very little surface contact with the water compared to drill
ships and semi-submersible drill rigs; therefore, lattice-legged jack-
up drill rigs are relatively quiet (Richardson et al., 1995; Spence et
al., 2007).
The Spartan 151, the only other jack-up drilling rig operating in
the Cook Inlet, was hydro-acoustically measured by Marine Acoustics,
Inc. (2011) while operating in 2011. The survey results showed that
continuous noise levels exceeding 120 dB re 1[mu]Pa extended out only
164 ft (50 m), and that this sound was largely associated with the
diesel engines used as hotel power generators.
The Endeavour was hydro-acoustically tested during drilling
activities by Illingworth and Rodkin (2013a) in May 2013 while the rig
was operating at a lower Cook Inlet well site (Cosmopolitan
1). The results from the sound source verification indicated
that noise generated from drilling or generators were below ambient
sound levels. The generators used on the Endeavour are mounted on
pedestals specifically to reduce noise transfer through the
infrastructure, and they are enclosed in an insulated engine room,
which may further have reduced underwater sound transmission to levels
below those generated by the Spartan 151. Also, as mentioned above, the
lattice legs limit transfer of noise generated from the drilling table
to the water.
The sound source verification revealed that the submersed deep-well
pumps that charge the fire-suppression system and cool the generators
(in a closed water system) generate sound levels exceeding 120 dB re
1[mu]Pa out a distance of approximately 984 ft (300 m). It was not
clear at the time of measurements whether the sound was a direct result
of the pumps or was from the systems discharge water falling
approximately 40 ft (12 m) from the deck. Thus, after the falling water
was enclosed in pipe extending below the water surface in an effort to
reduce sound levels, the pump noise levels were re-measured in June
2013 (I&R, 2013b) with results indicating that piping the falling water
had a modicum of effect on reducing underwater sound levels;
nevertheless, the 120-dB radius still extended out to 853 ft (260 m) in
certain directions. Thus, neither drilling operations nor running
generators on the Endeavour drill rig generate underwater sound levels
exceeding 120 dB re 1[mu]Pa. However, the Endeavour's submersed deep-
well pumps generate continuous sound exceeding 120 dB re 1[mu]Pa to a
maximum distance of 853 ft (260 m).
4. Vertical Seismic Profiling
Once a well is drilled, accurate follow-up seismic data can be
collected by placing a receiver at known depths in the borehole and
shooting a seismic airgun at the surface near the borehole. This
gathered data provides not only high resolution images of the
geological layers penetrated by the borehole but can be used to
accurately correlate (or correct) the original surface seismic data.
The procedure is known as VSP.
Buccaneer intends to conduct VSP operations at the end of drilling
each
[[Page 19254]]
well using an array of airguns with total volumes of between 600 and
880 cubic inches (in\3\). Each VSP operation is expected to last less
than 1 or 2 days. Assuming a 1-meter source level of 227 dB re 1[mu]Pa
(based on manufacturer's specifications) for an 880 in\3\ array and
using Collins et al.'s (2007) transmission loss model for Cook Inlet
(227--18.4 Log(R)--0.00188), the 190 dB radius from the source was
estimated at 330 ft (100 m), the 180 dB radius at 1,090 ft (332 m), and
the 160 dB radius at 1.53 mi (2.46 km).
Illingworth and Rodkin (2013c) measured the underwater sound levels
associated with the July 2013 VSP operation using a 720 in\3\ array and
found sound levels exceeding 160 dB re 1 [mu]Pa (rms) extended out 1.54
mi (2.47 km), virtually identical to the modeled distance. The measured
radius to 190 dB was 246 ft (75 m) and to 180 dB was 787 ft (240 m).
The best fit model for the empirical data was 227--19.75 log(R)--0.0
(I&R 2013c).
5. Helicopter and Supply Vessel Support
Helicopter logistics for project operations will include
transportation for personnel, groceries, and supplies. Helicopter
support will consist of a twin turbine Bell 212 (or equivalent)
helicopter certified for instrument flight rules land and over water
operations. Helicopter crews and support personnel will be housed in
existing Kenai area facilities. The helicopter will be based at the
Kenai Airport to support rig crew changes and cargo handling. Fueling
will take place at these facilities. No helicopter refueling will take
place on the rig.
Helicopter flights to and from the rig are expected to average two
per day. Flight routes will follow a direct route to and from the rig
location, and flight heights will be maintained 1,000 to 1,500 feet
above ground level to avoid take of marine mammals (Richardson et al.,
1995). At these altitudes, there are not expected to be impacts from
sound generation on marine mammals. The aircraft will be dedicated to
the drilling operation and will be available for service 24 hours per
day. A replacement aircraft will be available when major maintenance
items are scheduled.
Major supplies will be staged on-shore at the Kenai OSK Dock.
Required supplies and equipment will be moved from the staging area by
contracted supply vessels and loaded aboard the rig when the rig is
established on a drilling location. Major supplies will include fuel,
drilling water, mud materials, cement, casing, and well service
equipment. Supply vessels also will be outfitted with fire-fighting
systems as part of fire prevention and control as required by Cook
Inlet Spill Prevention and Response, Inc. The specific supply vessels
have not been identified; however, typical offshore drilling support
work vessels are of steel construction with strengthened hulls to give
the capability of working in extreme conditions. Additional information
about logistics and fuel and waste management can be found in Section
1.2 of Buccaneer's IHA application.
Description of Marine Mammals in the Area of the Specified Activity
The marine mammal species under NMFS's jurisdiction that could
occur near the exploratory drilling sites in upper Cook Inlet include
two cetacean species, both odontocetes (toothed whales): beluga whale
(Delphinapterus leucas) and harbor porpoise (Phocoena phocoena) and one
pinniped species: harbor seal (Phoca vitulina richardsi). The marine
mammal species that is likely to be encountered most widely (in space
and time) throughout the period of the planned surveys is the harbor
seal. While killer whales (Orcinus orca) and Steller sea lions
(Eumetopias jubatus) have been sighted in upper Cook Inlet, their
occurrence is considered rare in that portion of the Inlet. There have
also been a few sightings in the last couple of years of gray whales
(Eschrichtius robustus) in the upper inlet; however occurrence is rare.
Gray whales, killer whales, Steller sea lions, minke whales
(Balaenoptera acutorostrata), and Dall's porpoises (Phocoenoides dalli)
are more likely to occur in lower Cook Inlet (where rig towing would
occur).
Of these marine mammal species, Cook Inlet beluga whales and the
western distinct population segment (DPS) of Steller sea lions are
listed as endangered under the Endangered Species Act (ESA). The
eastern DPS was recently removed from the endangered species list (78
FR 66139, November 4, 2013) but currently retains its status as
``depleted'' under the MMPA along with the western DPS and Cook Inlet
beluga whales.
Despite these designations, Cook Inlet beluga whales and the
western DPS of Steller sea lions have not made significant progress
towards recovery. Data indicate that the Cook Inlet population of
beluga whales has been decreasing at a rate of 1.1 percent annually
between 2001 and 2011 (Allen and Angliss, 2013). A recent review of the
status of the population indicated that there is an 80% chance that the
population will decline further (Hobbs and Shelden 2008). Counts of
non-pup Steller sea lions at trend sites in the Alaska western stock
increased 11% from 2000 to 2004 (Allen and Angliss, 2013). These were
the first region-wide increases for the western stock since
standardized surveys began in the 1970s and were due to increased or
stable counts in all regions except the western Aleutian Islands.
Between 2004 and 2008, Alaska western non-pup counts increased only 3%:
eastern Gulf of Alaska (Prince William Sound area) counts were higher
and Kenai Peninsula through Kiska Island counts were stable, but
western Aleutian counts continued to decline. Johnson (2010) analyzed
western Steller sea lion population trends in Alaska and concluded that
the overall 2000-2008 trend was a decline 1.5% per year; however, there
continues to be considerable regional variability in recent trends
(Allen and Angliss, 2013). NMFS has not been able to complete a non-pup
survey of the AK western stock since 2008, due largely to weather and
closure of the Air Force base on Shemya in 2009 and 2010.
Pursuant to the ESA, critical habitat has been designated for Cook
Inlet beluga whales and Steller sea lions. The proposed action falls
within critical habitat designated in Cook Inlet for beluga whales but
is not within critical habitat designated for Steller sea lions.
Buccaneer's Southern Cross and Tyonek Deep well sites occur in areas
identified as Area 2 in the critical habitat designation. The wells are
located south of the Area 1 critical habitat designation where belugas
are particularly vulnerable to impacts due to their high seasonal
densities and the biological importance of the area for foraging,
nursery, and predator avoidance. Area 2 is based on dispersed fall and
winter feeding and transit areas in waters where whales typically
appear in smaller densities or deeper waters (76 FR 20180, April 11,
2011).
Buccaneer did not request take of beluga whales or Steller sea
lions. Informal consultation pursuant to section 7 of the ESA was
conducted for this project, and it was determined that the activity is
not likely to adversely affect listed species or critical habitat based
upon the nature of the activities and specific mitigation measures to
ensure that take of these species or adverse habitat impacts are
unlikely. This is discussed further in the ``Proposed Mitigation''
section later in this document.
Other species of mysticetes that have been observed infrequently in
lower Cook Inlet include: humpback whale (Megaptera novaeangliae) and
fin whale (Balaenoptera physalus). Because of
[[Page 19255]]
their infrequent occurrence Cook Inlet, they are not included in this
proposed IHA notice. Sea otters also occur in Cook Inlet. However, sea
otters are managed by the U.S. Fish and Wildlife Service and are
therefore not considered further in this proposed IHA notice.
Information summaries for the species for which take is requested is
provided next.
Cetaceans
1. Killer Whales
In general, killer whales are rare in upper Cook Inlet, where
transient killer whales are known to feed on beluga whales, and
resident killer whales are known to feed on anadromous fish (Shelden et
al., 2003). The availability of these prey species largely determines
the likeliest times for killer whales to be in the area. Between 1993
and 2004, 23 sightings of killer whales were reported in the lower Cook
Inlet during aerial surveys by Rugh et al. (2005). Surveys conducted
over a span of 20 years by Shelden et al. (2003) reported 11 sightings
in upper Cook Inlet between Turnagain Arm, Susitna Flats, and Knik Arm.
No killer whales were spotted during recent surveys by Funk et al.
(2005), Ireland et al. (2005), Brueggeman et al. (2007a, 2007b, 2008),
or Prevel Ramos et al. (2006, 2008). Eleven killer whale strandings
have been reported in Turnagain Arm, six in May 1991 and five in August
1993. Therefore, very few killer whales, if any, are expected to
approach or be in the vicinity of the action area.
2. Harbor Porpoise
The most recent estimated density for harbor porpoises in Cook
Inlet is 7.2 per 1,000 km\2\ (Dahlheim et al., 2000) indicating that
only a small number use Cook Inlet. Harbor porpoise have been reported
in lower Cook Inlet from Cape Douglas to the West Foreland, Kachemak
Bay, and offshore (Rugh et al., 2005). Small numbers of harbor
porpoises have been consistently reported in upper Cook Inlet between
April and October, except for a recent survey that recorded higher than
usual numbers (Prevel Ramos et al., 2008). Prevel Ramos et al. (2008)
reported 17 harbor porpoises from spring to fall 2006, while other
studies reported 14 in the spring of 2007 (Brueggeman et al. 2007) and
12 in the fall of 2007 (Brueggeman et al. 2008). During the spring and
fall of 2007, 129 harbor porpoises were reported between Granite Point
and the Susitna River; however, the reason for the increase in numbers
of harbor porpoise in the upper Cook Inlet remains unclear and the
disparity with the result of past sightings suggests that it may be an
anomaly. The spike in reported sightings occurred in July, which was
followed by sightings of 79 harbor porpoises in August, 78 in
September, and 59 in October 2007. It is important to note that the
number of porpoises counted more than once was unknown, which suggests
that the actual numbers are likely smaller than those reported. In
addition, recent passive acoustic research in Cook Inlet by the Alaska
Department of Fish and Game and the National Marine Mammal Laboratory
have indicated that harbor porpoises occur in the area more frequently
than previously thought, particularly in the West Foreland area in the
spring (NMFS 2011); however overall numbers are still unknown at this
time.
3. Gray Whale
The gray whale is a large baleen whale known to have one of the
longest migrations of any mammal. This whale can be found all along the
shallow coastal waters of the North Pacific Ocean.
The Eastern North Pacific stock, which includes those whales that
travel along the coast of Alaska, was delisted from the ESA in 1994
after a distinction was made between the western and eastern
populations (59 FR 31094, June 16, 1994). It is estimated that
approximately 18,000 individuals exist in the eastern stock (Allen and
Angliss, 2012).
Although observations of gray whales are rare within Cook Inlet,
marine mammal observers noted individual gray whales on nine occasions
in upper Cook Inlet in 2012 while conducting marine mammal monitoring
for seismic survey activities under an IHA NMFS issued to Apache Alaska
Corporation: four times in May; twice in June; and three times in July
(Apache, 2013). Annual surveys conducted by NMFS in Cook Inlet since
1993 have resulted in a total of five gray whale sightings (Rugh et
al., 2005). Although Cook Inlet is not believed to comprise either
essential feeding or social ground, and gray whales are typically not
observed within upper Cook Inlet, there may be some encounters in lower
Cook Inlet during towing activities and perhaps an incidental encounter
in the upper Inlet.
4. Minke Whale
Minke whales are the smallest of the rorqual group of baleen
whales. There are no population estimates for the North Pacific,
although estimates have been made for some portions of Alaska. Zerbini
et al. (2006) estimated the coastal population between Kenai Fjords and
the Aleutian Islands at 1,233 animals. During Cook Inlet-wide aerial
surveys conducted from 1993 to 2004, minke whales were encountered only
twice (1998, 1999), both times off Anchor Point 16 mi northwest of
Homer. A minke whale was also reported off Cape Starichkof in 2011 (A.
Holmes, pers. comm.) and 2013 (E. Fernandez and C. Hesselbach, pers.
comm.), suggesting this location is regularly used by minke whales,
including during the winter. There are no records north of Cape
Starichkof, and this species is unlikely to be seen in upper Cook
Inlet. There is a chance of encountering this whale during towing
operations through lower Cook Inlet.
5. Dall's Porpoise
Dall's porpoise are widely distributed throughout the North Pacific
Ocean including Alaska, although they are not found in upper Cook Inlet
and the shallower waters of the Bering, Chukchi, and Beaufort Seas
(Allen and Angliss, 2013). The Alaskan population has been estimated at
83,400 animals (Allen and Angliss, 2013), making it one of the more
common cetaceans in the state. Dall's porpoise have been observed in
lower Cook Inlet, including Kachemak Bay and near Anchor Point (Glenn
Johnson, pers. comm.), but sightings there are rare. There is only the
remote chance that Dall's porpoise might be observed during Buccaneer
towing operations through lower Cook Inlet.
Pinnipeds
1. Harbor Seals
Harbor seals inhabit the coastal and estuarine waters of Cook Inlet
and are one of the more common marine mammal species in Alaskan waters.
Harbor seals are non-migratory; their movements are associated with
tides, weather, season, food availability, and reproduction. The major
haulout sites for harbor seals are located in lower Cook Inlet, and
their presence in the upper inlet coincides with seasonal runs of prey
species. For example, harbor seals are commonly observed along the
Susitna River and other tributaries along upper Cook Inlet during the
eulachon and salmon migrations (NMFS, 2003). During aerial surveys of
upper Cook Inlet in 2001, 2002, and 2003, harbor seals were observed 24
to 96 km (15 to 60 mi) south-southwest of Anchorage at the Chickaloon,
Little Susitna, Susitna, Ivan, McArthur, and Beluga Rivers (Rugh et
al., 2005). Montgomery et al. (2007) recorded over 200 haulout sites in
lower Cook Inlet alone. However, only a few dozen to a couple hundred
seals seasonally occur in upper Cook
[[Page 19256]]
Inlet (Rugh et al., 2005), mostly at the mouth of the Susitna River
where their numbers vary in concert with the spring eulachon and summer
salmon runs (Nemeth et al., 2007, Boveng et al., 2012). Montgomery et
al. (2007) also found seals elsewhere in Cook Inlet to move in response
to local steelhead and salmon runs. However, aerial surveys conducted
in June 2013 for the proposed Susitna Dam project noted nearly 700
harbor seals in the Susitna Delta region (Alaska Energy Authority,
2013). Harbor seals may be encountered during rig tows to and from Cape
Starichkof, and possibly during drilling in upper Cook Inlet.
As mentioned previously, take of marine mammals listed under the
ESA will not occur because of mitigation measures to ensure no take of
those species. Buccaneer's application contains information on the
status, distribution, seasonal distribution, and abundance of each of
the species under NMFS jurisdiction mentioned in this document. Please
refer to the application for that information (see ADDRESSES).
Additional information can also be found in the NMFS Stock Assessment
Reports (SAR). The Alaska 2012 SAR is available on the Internet at:
https://www.nmfs.noaa.gov/pr/sars/pdf/ak2012.pdf.
Potential Effects of the Specified Activity on Marine Mammals
This section includes a summary and discussion of the ways that the
types of stressors associated with the specified activity (e.g.,
driving of the conductor pipe; exploratory drilling; towing of the
jack-up drill rig; and VSP) have been observed to or are thought to
impact marine mammals. This section may include a discussion of known
effects that do not rise to the level of an MMPA take (for example,
with acoustics, we may include a discussion of studies that showed
animals not reacting at all to sound or exhibiting barely measurable
avoidance). The discussion may also include reactions that we consider
to rise to the level of a take and those that we do not consider to
rise to the level of a take. This section is intended as a background
of potential effects and does not consider either the specific manner
in which this activity will be carried out or the mitigation that will
be implemented or how either of those will shape the anticipated
impacts from this specific activity. The ``Estimated Take by Incidental
Harassment'' section later in this document will include a quantitative
analysis of the number of individuals that are expected to be taken by
this activity. The ``Negligible Impact Analysis'' section will include
the analysis of how this specific activity will impact marine mammals
and will consider the content of this section, the ``Estimated Take by
Incidental Harassment'' section, the ``Mitigation'' section, and the
``Anticipated Effects on Marine Mammal Habitat'' section to draw
conclusions regarding the likely impacts of this activity on the
reproductive success or survivorship of individuals and from that on
the affected marine mammal populations or stocks.
The likely or possible impacts of the proposed drilling program in
upper Cook Inlet on marine mammals could involve both non-acoustic and
acoustic stressors. Potential non-acoustic stressors could result from
the physical presence of the equipment and personnel. Petroleum
development and associated activities introduce sound into the marine
environment. Impacts to marine mammals are expected to primarily be
acoustic in nature. Potential acoustic effects on marine mammals relate
to sound produced by drilling activity, conductor pipe driving, and rig
towing, as well as the VSP airgun array.
Acoustic Impacts
When considering the influence of various kinds of sound on the
marine environment, it is necessary to understand that different kinds
of marine life are sensitive to different frequencies of sound. Based
on available behavioral data, audiograms have been derived using
auditory evoked potentials, anatomical modeling, and other data,
Southall et al. (2007) designate ``functional hearing groups'' for
marine mammals and estimate the lower and upper frequencies of
functional hearing of the groups. The functional groups and the
associated frequencies are indicated below (though animals are less
sensitive to sounds at the outer edge of their functional range and
most sensitive to sounds of frequencies within a smaller range
somewhere in the middle of their functional hearing range):
Low frequency cetaceans (13 species of mysticetes):
Functional hearing is estimated to occur between approximately 7 Hz and
30 kHz;
Mid-frequency cetaceans (32 species of dolphins, six
species of larger toothed whales, and 19 species of beaked and
bottlenose whales): Functional hearing is estimated to occur between
approximately 150 Hz and 160 kHz;
High frequency cetaceans (eight species of true porpoises,
six species of river dolphins, Kogia, the franciscana, and four species
of cephalorhynchids): Functional hearing is estimated to occur between
approximately 200 Hz and 180 kHz;
Phocid pinnipeds in Water: Functional hearing is estimated
to occur between approximately 75 Hz and 100 kHz; and
Otariid pinnipeds in Water: Functional hearing is
estimated to occur between approximately 100 Hz and 40 kHz.
As mentioned previously in this document, six marine mammal species
(five cetacean and one phocid pinniped) may occur in the exploratory
drilling area or in the rig tow area. Of the five cetacean species
likely to occur in the proposed project area and for which take is
requested, two are classified as low-frequency cetaceans (i.e., minke
and gray whales), one is classified as a mid-frequency cetacean (i.e.,
killer whale), and two are classified as a high-frequency cetaceans
(i.e., harbor and Dall's porpoises) (Southall et al., 2007). A species'
functional hearing group is a consideration when we analyze the effects
of exposure to sound on marine mammals.
1. Tolerance
Numerous studies have shown that underwater sounds from industry
activities are often readily detectable by marine mammals in the water
at distances of many kilometers. Numerous studies have also shown that
marine mammals at distances more than a few kilometers away often show
no apparent response to industry activities of various types (Miller et
al., 2005; Bain and Williams, 2006). This is often true even in cases
when the sounds must be readily audible to the animals based on
measured received levels and the hearing sensitivity of that mammal
group. Although various baleen whales, toothed whales, and (less
frequently) pinnipeds have been shown to react behaviorally to
underwater sound such as airgun pulses or vessels under some
conditions, at other times mammals of all three types have shown no
overt reactions (e.g., Malme et al., 1986; Richardson et al., 1995;
Madsen and Mohl, 2000; Croll et al., 2001; Jacobs and Terhune, 2002;
Madsen et al., 2002; Miller et al., 2005). Weir (2008) observed marine
mammal responses to seismic pulses from a 24 airgun array firing a
total volume of either 5,085 in\3\ or 3,147 in\3\ in Angolan waters
between August 2004 and May 2005. Weir recorded a total of 207
sightings of humpback whales (n = 66), sperm whales (n = 124), and
Atlantic spotted dolphins (n = 17) and reported that there were no
significant differences in encounter rates (sightings/hr) for
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humpback and sperm whales according to the airgun array's operational
status (i.e., active versus silent). The airgun arrays used in the Weir
(2008) study were much larger than the array proposed for use during
the limited VSP (total discharge volumes of 600 to 880 in\3\ for 1 to 2
days per well). In general, pinnipeds and small odontocetes seem to be
more tolerant of exposure to some types of underwater sound than are
baleen whales. Richardson et al. (1995b) found that vessel noise does
not seem to strongly affect pinnipeds that are already in the water.
Richardson et al. (1995b) went on to explain that seals on haul-outs
sometimes respond strongly to the presence of vessels and at other
times appear to show considerable tolerance of vessels.
2. Masking
Masking is the obscuring of sounds of interest by other sounds,
often at similar frequencies. Marine mammals use acoustic signals for a
variety of purposes, which differ among species, but include
communication between individuals, navigation, foraging, reproduction,
avoiding predators, and learning about their environment (Erbe and
Farmer, 2000; Tyack, 2000). Masking, or auditory interference,
generally occurs when sounds in the environment are louder than, and of
a similar frequency as, auditory signals an animal is trying to
receive. Masking is a phenomenon that affects animals that are trying
to receive acoustic information about their environment, including
sounds from other members of their species, predators, prey, and sounds
that allow them to orient in their environment. Masking these acoustic
signals can disturb the behavior of individual animals, groups of
animals, or entire populations.
Masking occurs when anthropogenic sounds and signals (that the
animal utilizes) overlap at both spectral and temporal scales. The
sounds generated by the proposed equipment for the exploratory drilling
program will consist of low frequency sources (most under 500 Hz).
Lower frequency man-made sounds are more likely to affect detection of
communication calls and other potentially important natural sounds such
as surf and prey noise. There is little concern regarding masking near
the jack-up rig during exploratory drilling operations, as the species
most likely to be found in the vicinity are mid- to high-frequency
cetaceans or pinnipeds and not low-frequency cetaceans. Additionally,
masking is not expected to be a concern from airgun usage due to the
brief duration of use (less than a day to up to 2 days per well) and
the low-frequency sounds that are produced by the airguns. However, at
long distances (over tens of kilometers away), due to multipath
propagation and reverberation, the durations of airgun pulses can be
``stretched'' to seconds with long decays (Madsen et al., 2006),
although the intensity of the sound is greatly reduced.
This could affect communication signals used by low frequency
mysticetes when they occur near the noise band and thus reduce the
communication space of animals (e.g., Clark et al., 2009) and cause
increased stress levels (e.g., Foote et al., 2004; Holt et al., 2009);
however, no baleen whales are expected to occur within the proposed
action area in the upper Inlet. A few may be encountered in the lower
Inlet during the rig towing. Marine mammals are thought to sometimes be
able to compensate for masking by adjusting their acoustic behavior by
shifting call frequencies, and/or increasing call volume and
vocalization rates. For example, blue whales are found to increase call
rates when exposed to seismic survey noise in the St. Lawrence Estuary
(Di Iorio and Clark, 2010). The North Atlantic right whales (Eubalaena
glacialis) exposed to high shipping noise increase call frequency
(Parks et al., 2007), while some humpback whales respond to low-
frequency active sonar playbacks by increasing song length (Miller el
al., 2000). Additionally, beluga whales have been known to change their
vocalizations in the presence of high background noise possibly to
avoid masking calls (Au et al., 1985; Lesage et al., 1999; Scheifele et
al., 2005). Although some degree of masking is inevitable when high
levels of manmade broadband sounds are introduced into the sea, marine
mammals have evolved systems and behavior that function to reduce the
impacts of masking. Structured signals, such as the echolocation click
sequences of small toothed whales, may be readily detected even in the
presence of strong background noise because their frequency content and
temporal features usually differ strongly from those of the background
noise (Au and Moore, 1988, 1990). The components of background noise
that are similar in frequency to the sound signal in question primarily
determine the degree of masking of that signal.
Redundancy and context can also facilitate detection of weak
signals. These phenomena may help marine mammals detect weak sounds in
the presence of natural or manmade noise. Most masking studies in
marine mammals present the test signal and the masking noise from the
same direction. The sound localization abilities of marine mammals
suggest that, if signal and noise come from different directions,
masking would not be as severe as the usual types of masking studies
might suggest (Richardson et al., 1995). The dominant background noise
may be highly directional if it comes from a particular anthropogenic
source such as a ship or industrial site. Directional hearing may
significantly reduce the masking effects of these sounds by improving
the effective signal-to-noise ratio. In the cases of higher frequency
hearing by the bottlenose dolphin, beluga whale, and killer whale,
empirical evidence confirms that masking depends strongly on the
relative directions of arrival of sound signals and the masking noise
(Penner et al., 1986; Dubrovskiy, 1990; Bain et al., 1993; Bain and
Dahlheim, 1994). Toothed whales, and probably other marine mammals as
well, have additional capabilities besides directional hearing that can
facilitate detection of sounds in the presence of background noise.
There is evidence that some toothed whales can shift the dominant
frequencies of their echolocation signals from a frequency range with a
lot of ambient noise toward frequencies with less noise (Au et al.,
1974, 1985; Moore and Pawloski, 1990; Thomas and Turl, 1990; Romanenko
and Kitain, 1992; Lesage et al., 1999). A few marine mammal species are
known to increase the source levels or alter the frequency of their
calls in the presence of elevated sound levels (Dahlheim, 1987; Au,
1993; Lesage et al., 1993, 1999; Terhune, 1999; Foote et al., 2004;
Parks et al., 2007, 2009; Di Iorio and Clark, 2009; Holt et al., 2009).
These data demonstrating adaptations for reduced masking pertain
mainly to the very high frequency echolocation signals of toothed
whales. There is less information about the existence of corresponding
mechanisms at moderate or low frequencies or in other types of marine
mammals. For example, Zaitseva et al. (1980) found that, for the
bottlenose dolphin, the angular separation between a sound source and a
masking noise source had little effect on the degree of masking when
the sound frequency was 18 kHz, in contrast to the pronounced effect at
higher frequencies. Directional hearing has been demonstrated at
frequencies as low as 0.5-2 kHz in several marine mammals, including
killer whales (Richardson et al., 1995a). This ability may be useful in
reducing masking at these frequencies. In summary, high
[[Page 19258]]
levels of sound generated by anthropogenic activities may act to mask
the detection of weaker biologically important sounds by some marine
mammals. This masking may be more prominent for lower frequencies. For
higher frequencies, such as that used in echolocation by toothed
whales, several mechanisms are available that may allow them to reduce
the effects of such masking.
3. Behavioral Disturbance
Behavioral responses to sound are highly variable and context-
specific. Many different variables can influence an animal's perception
of and response to (in both nature and magnitude) an acoustic event. An
animal's prior experience with a sound or sound source affects whether
it is less likely (habituation) or more likely (sensitization) to
respond to certain sounds in the future (animals can also be innately
pre-disposed to respond to certain sounds in certain ways; Southall et
al., 2007). Related to the sound itself, the perceived nearness of the
sound, bearing of the sound (approaching vs. retreating), similarity of
a sound to biologically relevant sounds in the animal's environment
(i.e., calls of predators, prey, or conspecifics), and familiarity of
the sound may affect the way an animal responds to the sound (Southall
et al., 2007). Individuals (of different age, gender, reproductive
status, etc.) among most populations will have variable hearing
capabilities and differing behavioral sensitivities to sounds that will
be affected by prior conditioning, experience, and current activities
of those individuals. Often, specific acoustic features of the sound
and contextual variables (i.e., proximity, duration, or recurrence of
the sound or the current behavior that the marine mammal is engaged in
or its prior experience), as well as entirely separate factors such as
the physical presence of a nearby vessel, may be more relevant to the
animal's response than the received level alone.
Exposure of marine mammals to sound sources can result in (but is
not limited to) no response or any of the following observable
responses: Increased alertness; orientation or attraction to a sound
source; vocal modifications; cessation of feeding; cessation of social
interaction; alteration of movement or diving behavior; avoidance;
habitat abandonment (temporary or permanent); and, in severe cases,
panic, flight, stampede, or stranding, potentially resulting in death
(Southall et al., 2007). The biological significance of many of these
behavioral disturbances is difficult to predict, especially if the
detected disturbances appear minor. However, the consequences of
behavioral modification have the potential to be biologically
significant if the change affects growth, survival, or reproduction.
Examples of significant behavioral modifications include:
Drastic change in diving/surfacing patterns (such as those
thought to be causing beaked whale stranding due to exposure to
military mid-frequency tactical sonar);
Habitat abandonment due to loss of desirable acoustic
environment; and
Cessation of feeding or social interaction.
Detailed studies regarding responses to anthropogenic sound have
been conducted on humpback, gray, and bowhead whales and ringed seals.
Less detailed data are available for some other species of baleen
whales, sperm whales, small toothed whales, and sea otters. The
following sub-sections provide examples of behavioral responses that
provide an idea of the variability in behavioral responses that would
be expected given the different sensitivities of marine mammal species
to sound. However, baleen whales are unlikely to occur in the vicinity
of the well sites and are only somewhat likely to occur in the lower
portions of Cook Inlet during rig towing activities.
Baleen Whales--Richardson et al. (1995a) reported changes in
surfacing and respiration behavior and the occurrence of turns during
surfacing in bowhead whales exposed to playback of underwater sound
from drilling activities. These behavioral effects were localized and
occurred at distances up to 1.2-2.5 mi (2-4 km).
Richardson et al. (2008) reported a slight change in the
distribution of bowhead whale calls in response to operational sounds
on BP's Northstar Island. The southern edge of the call distribution
ranged from 0.47 to 1.46 mi (0.76 to 2.35 km) farther offshore,
apparently in response to industrial sound levels. This result however,
was only achieved after intensive statistical analyses, and it is not
clear that this represented a biologically significant effect.
Richardson et al. (1995a) and Moore and Clarke (2002) reviewed a
few studies that observed responses of gray whales to aircraft. Cow-
calf pairs were quite sensitive to a turboprop survey flown at 1,000 ft
(305 m) altitude on the Alaskan summering grounds. In that survey,
adults were seen swimming over the calf, or the calf swam under the
adult (Ljungblad et al., 1983, cited in Richardson et al., 1995b and
Moore and Clarke, 2002). However, when the same aircraft circled for
more than 10 minutes at 1,050 ft (320 m) altitude over a group of
mating gray whales, no reactions were observed (Ljungblad et al., 1987,
cited in Moore and Clarke, 2002). Malme et al. (1984, cited in
Richardson et al., 1995b and Moore and Clarke, 2002) conducted playback
experiments on migrating gray whales. They exposed the animals to
underwater noise recorded from a Bell 212 helicopter (estimated
altitude=328 ft [100 m]), at an average of three simulated passes per
minute. The authors observed that whales changed their swimming course
and sometimes slowed down in response to the playback sound but
proceeded to migrate past the transducer. Migrating gray whales did not
react overtly to a Bell 212 helicopter at greater than 1,394 ft (425 m)
altitude, occasionally reacted when the helicopter was at 1,000-1,198
ft (305-365 m), and usually reacted when it was below 825 ft (250 m;
Southwest Research Associates, 1988, cited in Richardson et al., 1995b
and Moore and Clarke, 2002). Reactions noted in that study included
abrupt turns or dives or both. Green et al. (1992, cited in Richardson
et al., 1995b) observed that migrating gray whales rarely exhibited
noticeable reactions to a straight-line overflight by a Twin Otter at
197 ft (60 m) altitude. Restrictions on aircraft altitude will be part
of the proposed mitigation measures (described in the ``Proposed
Mitigation'' section later in this document) during the proposed
drilling activities, and overflights are likely to have little or no
disturbance effects on baleen whales. Any disturbance that may occur
would likely be temporary and localized.
Southall et al. (2007, Appendix C) reviewed a number of papers
describing the responses of marine mammals to non-pulsed sound, such as
that produced during exploratory drilling operations. In general,
little or no response was observed in animals exposed at received
levels from 90-120 dB re 1 [mu]Pa (rms). Probability of avoidance and
other behavioral effects increased when received levels were from 120-
160 dB re 1 [mu]Pa (rms). Some of the relevant reviews contained in
Southall et al. (2007) are summarized next.
Baker et al. (1982) reported some avoidance by humpback whales to
vessel noise when received levels were 110-120 dB (rms) and clear
avoidance at 120-140 dB (sound measurements were not provided by Baker
but were based on measurements of identical vessels by Miles and Malme,
1983).
Malme et al. (1983, 1984) used playbacks of sounds from helicopter
[[Page 19259]]
overflight and drilling rigs and platforms to study behavioral effects
on migrating gray whales. Received levels exceeding 120 dB induced
avoidance reactions. Malme et al. (1984) calculated 10%, 50%, and 90%
probabilities of gray whale avoidance reactions at received levels of
110, 120, and 130 dB, respectively. Malme et al. (1986) observed the
behavior of feeding gray whales during four experimental playbacks of
drilling sounds (50 to 315 Hz; 21- min overall duration and 10% duty
cycle; source levels of 156-162 dB). In two cases for received levels
of 100-110 dB, no behavioral reaction was observed. However, avoidance
behavior was observed in two cases where received levels were 110-120
dB.
Richardson et al. (1990) performed 12 playback experiments in which
bowhead whales in the Alaskan Arctic were exposed to drilling sounds.
Whales generally did not respond to exposures in the 100 to 130 dB
range, although there was some indication of minor behavioral changes
in several instances.
McCauley et al. (1996) reported several cases of humpback whales
responding to vessels in Hervey Bay, Australia. Results indicated clear
avoidance at received levels between 118 to 124 dB in three cases for
which response and received levels were observed/measured.
Palka and Hammond (2001) analyzed line transect census data in
which the orientation and distance off transect line were reported for
large numbers of minke whales. The authors developed a method to
account for effects of animal movement in response to sighting
platforms. Minor changes in locomotion speed, direction, and/or diving
profile were reported at ranges from 1,847 to 2,352 ft (563 to 717 m)
at received levels of 110 to 120 dB.
Biassoni et al. (2000) and Miller et al. (2000) reported behavioral
observations for humpback whales exposed to a low-frequency sonar
stimulus (160- to 330-Hz frequency band; 42-s tonal signal repeated
every 6 min; source levels 170 to 200 dB) during playback experiments.
Exposure to measured received levels ranging from 120 to 150 dB
resulted in variability in humpback singing behavior. Croll et al.
(2001) investigated responses of foraging fin and blue whales to the
same low frequency active sonar stimulus off southern California.
Playbacks and control intervals with no transmission were used to
investigate behavior and distribution on time scales of several weeks
and spatial scales of tens of kilometers. The general conclusion was
that whales remained feeding within a region for which 12 to 30 percent
of exposures exceeded 140 dB.
Frankel and Clark (1998) conducted playback experiments with
wintering humpback whales using a single speaker producing a low-
frequency ``M-sequence'' (sine wave with multiple-phase reversals)
signal in the 60 to 90 Hz band with output of 172 dB at 1 m. For 11
playbacks, exposures were between 120 and 130 dB re 1 [mu]Pa (rms) and
included sufficient information regarding individual responses. During
eight of the trials, there were no measurable differences in tracks or
bearings relative to control conditions, whereas on three occasions,
whales either moved slightly away from (n=1) or towards (n=2) the
playback speaker during exposure. The presence of the source vessel
itself had a greater effect than did the M-sequence playback.
Finally, Nowacek et al. (2004) used controlled exposures to
demonstrate behavioral reactions of northern right whales to various
non-pulse sounds. Playback stimuli included ship noise, social sounds
of conspecifics, and a complex, 18-min ``alert'' sound consisting of
repetitions of three different artificial signals. Ten whales were
tagged with calibrated instruments that measured received sound
characteristics and concurrent animal movements in three dimensions.
Five out of six exposed whales reacted strongly to alert signals at
measured received levels between 130 and 150 dB (i.e., ceased foraging
and swam rapidly to the surface). Two of these individuals were not
exposed to ship noise, and the other four were exposed to both stimuli.
These whales reacted mildly to conspecific signals. Seven whales,
including the four exposed to the alert stimulus, had no measurable
response to either ship sounds or actual vessel noise.
Baleen whale responses to pulsed sound (e.g., seismic airguns) have
been studied more thoroughly than responses to continuous sound (e.g.,
drill rigs). 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 greater distances (Miller
et al., 2005). However, baleen whales exposed to strong noise pulses
often react by deviating from their normal migration route (Richardson
et al., 1999). Migrating gray and bowhead whales were observed avoiding
the sound source by displacing their migration route to varying degrees
but within the natural boundaries of the migration corridors (Schick
and Urban, 2000; Richardson et al., 1999; Malme et al., 1983). Baleen
whale responses to pulsed sound however may depend on the type of
activity in which the whales are engaged. Some evidence suggests that
feeding bowhead whales may be more tolerant of underwater sound than
migrating bowheads (Miller et al., 2005; Lyons et al., 2009; Christie
et al., 2010).
Results of studies of gray, bowhead, and humpback whales have
determined that received levels of pulses in the 160-170 dB re 1 [mu]Pa
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 2.8-9 mi (4.5-14.5 km) from the source. For the much smaller
airgun array used during the VSP survey (total discharge volume between
600 and 880 in\3\), the distance to a received level of 160 dB re 1
[mu]Pa rms is estimated to be 1.53 mi (2.47 km). 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
have shown that some species of baleen whales, notably bowhead and
humpback whales, at times show strong avoidance at received levels
lower than 160-170 dB re 1 [mu]Pa rms.
Malme et al. (1986, 1988) studied the responses of feeding eastern
gray whales to pulses from a single 100 in\3\ airgun off St. Lawrence
Island in the northern Bering Sea. They estimated, based on small
sample sizes, that 50% of feeding gray whales ceased feeding at an
average received pressure level of 173 dB re 1 [mu] Pa on an
(approximate) rms basis, and that 10% 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 the distribution of feeding Western Pacific gray whales
off Sakhalin Island, Russia, during a seismic survey (Yazvenko et al.,
2007).
Data on short-term reactions (or lack of reactions) of cetaceans to
impulsive noises do not necessarily provide information about long-term
effects. While it is not certain whether impulsive noises affect
reproductive rate or distribution and habitat use in subsequent days or
years, certain species have continued to use areas ensonified by
airguns and have continued to increase in number despite successive
years of anthropogenic
[[Page 19260]]
activity in the area. 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). In any event, the brief exposures to sound
pulses from the proposed airgun source (the airguns will only be fired
for a few hours at a time over the course of 1 to 2 days per well) are
highly unlikely to result in prolonged effects.
Toothed Whales--Most toothed whales have the greatest hearing
sensitivity at frequencies much higher than that of baleen whales and
may be less responsive to low-frequency sound commonly associated with
oil and gas industry exploratory drilling activities. Richardson et al.
(1995a) reported that beluga whales did not show any apparent reaction
to playback of underwater drilling sounds at distances greater than
656-1,312 ft (200-400 m). Reactions included slowing down, milling, or
reversal of course after which the whales continued past the projector,
sometimes within 164-328 ft (50-100 m). The authors concluded (based on
a small sample size) that the playback of drilling sounds had no
biologically significant effects on migration routes of beluga whales
migrating through pack ice and along the seaward side of the nearshore
lead east of Point Barrow in spring.
At least six of 17 groups of beluga whales appeared to alter their
migration path in response to underwater playbacks of icebreaker sound
(Richardson et al., 1995a). Received levels from the icebreaker
playback were estimated at 78-84 dB in the \1/3\-octave band centered
at 5,000 Hz, or 8-14 dB above ambient. If beluga whales reacted to an
actual icebreaker at received levels of 80 dB, reactions would be
expected to occur at distances on the order of 6.2 mi (10 km). Finley
et al. (1990) also reported beluga avoidance of icebreaker activities
in the Canadian High Arctic at distances of 22-31 mi (35-50 km). In
addition to avoidance, changes in dive behavior and pod integrity were
also noted. However, no icebreakers will be used during this proposed
program.
Patenaude et al. (2002) reported changes in beluga whale diving and
respiration behavior, and some whales veered away when a helicopter
passed at <=820 ft (250 m) lateral distance at altitudes up to 492 ft
(150 m). However, some belugas showed no reaction to the helicopter.
Belugas appeared to show less response to fixed-wing aircraft than to
helicopter overflights.
In reviewing responses of cetaceans with best hearing in mid-
frequency ranges, which includes toothed whales, Southall et al. (2007)
reported that combined field and laboratory data for mid-frequency
cetaceans exposed to non-pulse sounds did not lead to a clear
conclusion about received levels coincident with various behavioral
responses. In some settings, individuals in the field showed profound
(significant) behavioral responses to exposures from 90-120 dB, while
others failed to exhibit such responses for exposure to received levels
from 120-150 dB. Contextual variables other than exposure received
level, and probable species differences, are the likely reasons for
this variability. Context, including the fact that captive subjects
were often directly reinforced with food for tolerating noise exposure,
may also explain why there was great disparity in results from field
and laboratory conditions--exposures in captive settings generally
exceeded 170 dB before inducing behavioral responses. A summary of some
of the relevant material reviewed by Southall et al. (2007) is next.
Buckstaff (2004) reported elevated dolphin whistle rates with
received levels from oncoming vessels in the 110 to 120 dB range in
Sarasota Bay, Florida. These hearing thresholds were apparently lower
than those reported by a researcher listening with towed hydrophones.
Morisaka et al. (2005) compared whistles from three populations of
Indo-Pacific bottlenose dolphins. One population was exposed to vessel
noise with spectrum levels of approximately 85 dB/Hz in the 1- to 22-
kHz band (broadband received levels approximately 128 dB) as opposed to
approximately 65 dB/Hz in the same band (broadband received levels
approximately 108 dB) for the other two sites. Dolphin whistles in the
noisier environment had lower fundamental frequencies and less
frequency modulation, suggesting a shift in sound parameters as a
result of increased ambient noise.
Morton and Symonds (2002) used census data on killer whales in
British Columbia to evaluate avoidance of non-pulse acoustic harassment
devices (AHDs). Avoidance ranges were about 2.5 mi (4 km). Also, there
was a dramatic reduction in the number of days ``resident'' killer
whales were sighted during AHD-active periods compared to pre- and
post-exposure periods and a nearby control site.
Monteiro-Neto et al. (2004) studied avoidance responses of tucuxi
(Sotalia fluviatilis), a freshwater dolphin, to Dukane[supreg] Netmark
acoustic deterrent devices. In a total of 30 exposure trials,
approximately five groups each demonstrated significant avoidance
compared to 20 pinger off and 55 no-pinger control trials over two
quadrats of about 0.19 mi\2\ (0.5 km\2\). Estimated exposure received
levels were approximately 115 dB.
Awbrey and Stewart (1983) played back semi-submersible drillship
sounds (source level: 163 dB) to belugas in Alaska. They reported
avoidance reactions at 984 and 4,921 ft (300 and 1,500 m) and approach
by groups at a distance of 2.2 mi (3.5 km; received levels were
approximately 110 to 145 dB over these ranges assuming a 15 log R
transmission loss). Similarly, Richardson et al. (1990) played back
drilling platform sounds (source level: 163 dB) to belugas in Alaska.
They conducted aerial observations of eight individuals among
approximately 100 spread over an area several hundred meters to several
kilometers from the sound source and found no obvious reactions.
Moderate changes in movement were noted for three groups swimming
within 656 ft (200 m) of the sound projector.
Two studies deal with issues related to changes in marine mammal
vocal behavior as a function of variable background noise levels. Foote
et al. (2004) found increases in the duration of killer whale calls
over the period 1977 to 2003, during which time vessel traffic in Puget
Sound, and particularly whale-watching boats around the animals,
increased dramatically. Scheifele et al. (2005) demonstrated that
belugas in the St. Lawrence River increased the levels of their
vocalizations as a function of the background noise level (the
``Lombard Effect'').
Several researchers conducting laboratory experiments on hearing
and the effects of non-pulse sounds on hearing in mid-frequency
cetaceans have reported concurrent behavioral responses. Nachtigall et
al. (2003) reported that noise exposures up to 179 dB and 55-min
duration affected the trained behaviors of a bottlenose dolphin
participating in a temporary threshold shift (TTS) experiment. Finneran
and Schlundt (2004) provided a detailed, comprehensive analysis of the
behavioral responses of belugas and bottlenose dolphins to 1-s tones
(received levels 160 to 202 dB) in the context of TTS experiments.
Romano et al. (2004) investigated the physiological responses of a
bottlenose dolphin and a beluga exposed to these tonal exposures and
demonstrated a decrease in blood cortisol levels during a series of
exposures between 130 and 201 dB. Collectively, the laboratory
observations suggested the onset of a behavioral
[[Page 19261]]
response at higher received levels than did field studies. The
differences were likely related to the very different conditions and
contextual variables between untrained, free-ranging individuals vs.
laboratory subjects that were rewarded with food for tolerating noise
exposure.
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 move away or
maintain a somewhat greater distance from the vessel when a large array
of airguns is operating than when it is silent (e.g., Goold, 1996a,b,c;
Calambokidis and Osmek, 1998; Stone, 2003). 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
6.2-12.4 mi (10-20 km) 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 6.2-12.4 mi (10-20
km) (Miller et al., 2005).
Observers stationed on seismic vessels operating off the United
Kingdom from 1997-2000 have provided data on the occurrence and
behavior of various toothed whales exposed to seismic pulses (Stone,
2003; Gordon et al., 2004). Killer whales were found to be
significantly farther from large airgun arrays during periods of
shooting compared with periods of no shooting. The displacement of the
median distance from the array was approximately 0.5 km (0.3 mi) or
more. Killer whales also appear to be more tolerant of seismic shooting
in deeper water.
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., 2002, 2005).
However, the animals tolerated high received levels of sound (p-p level
>200 dB re 1 [mu] Pa) before exhibiting aversive behaviors.
Pinnipeds--Pinnipeds generally seem to be less responsive to
exposure to industrial sound than most cetaceans. Pinniped responses to
underwater sound from some types of industrial activities such as
seismic exploration appear to be temporary and localized (Harris et
al., 2001; Reiser et al., 2009).
Southall et al. (2007) reviewed literature describing responses of
pinnipeds to non-pulsed sound and reported that the limited data
suggest exposures between approximately 90 and 140 dB generally do not
appear to induce strong behavioral responses in pinnipeds exposed to
non-pulse sounds in water; no data exist regarding exposures at higher
levels. It is important to note that among these studies, there are
some apparent differences in responses between field and laboratory
conditions. In contrast to the mid-frequency odontocetes, captive
pinnipeds responded more strongly at lower levels than did animals in
the field. Again, contextual issues are the likely cause of this
difference.
Jacobs and Terhune (2002) observed harbor seal reactions to AHDs
(source level in this study was 172 dB) deployed around aquaculture
sites. Seals were generally unresponsive to sounds from the AHDs.
During two specific events, individuals came within 141 and 144 ft (43
and 44 m) of active AHDs and failed to demonstrate any measurable
behavioral response; estimated received levels based on the measures
given were approximately 120 to 130 dB.
Costa et al. (2003) measured received noise levels from an Acoustic
Thermometry of Ocean Climate (ATOC) program sound source off northern
California using acoustic data loggers placed on translocated elephant
seals. Subjects were captured on land, transported to sea, instrumented
with archival acoustic tags, and released such that their transit would
lead them near an active ATOC source (at 939-m depth; 75-Hz signal with
37.5-Hz bandwidth; 195 dB maximum source level, ramped up from 165 dB
over 20 min) on their return to a haul-out site. Received exposure
levels of the ATOC source for experimental subjects averaged 128 dB
(range 118 to 137) in the 60- to 90-Hz band. None of the instrumented
animals terminated dives or radically altered behavior upon exposure,
but some statistically significant changes in diving parameters were
documented in nine individuals. Translocated northern elephant seals
exposed to this particular non-pulse source began to demonstrate subtle
behavioral changes at exposure to received levels of approximately 120
to 140 dB.
Kastelein et al. (2006) exposed nine captive harbor seals in an
approximately 82 x 98 ft (25 x 30 m) enclosure to non-pulse sounds used
in underwater data communication systems (similar to acoustic modems).
Test signals were frequency modulated tones, sweeps, and bands of noise
with fundamental frequencies between 8 and 16 kHz; 128 to 130 [ 3] dB source levels; 1- to 2-s duration [60-80 percent duty
cycle]; or 100 percent duty cycle. They recorded seal positions and the
mean number of individual surfacing behaviors during control periods
(no exposure), before exposure, and in 15-min experimental sessions (n
= 7 exposures for each sound type). Seals generally swam away from each
source at received levels of approximately 107 dB, avoiding it by
approximately 16 ft (5 m), although they did not haul out of the water
or change surfacing behavior. Seal reactions did not appear to wane
over repeated exposure (i.e., there was no obvious habituation), and
the colony of seals generally returned to baseline conditions following
exposure. The seals were not reinforced with food for remaining in the
sound field.
Potential effects to pinnipeds from aircraft activity could involve
both acoustic and non-acoustic effects. It is uncertain if the seals
react to the sound of the helicopter or to its physical presence flying
overhead. Typical reactions of hauled out pinnipeds to aircraft that
have been observed include looking up at the aircraft, moving on the
ice or land, entering a breathing hole or crack in the ice, or entering
the water. Ice seals hauled out on the ice have been observed diving
into the water when approached by a low-flying aircraft or helicopter
(Burns and Harbo, 1972, cited in Richardson et al., 1995a; Burns and
Frost, 1979, cited in Richardson et al., 1995a). Richardson et al.
(1995a) note that responses can vary based on differences in aircraft
type, altitude, and flight pattern.
Blackwell et al. (2004a) observed 12 ringed seals during low-
altitude overflights of a Bell 212 helicopter at Northstar in June and
July 2000 (9 observations took place concurrent with pipe-driving
activities). One seal showed no reaction to the aircraft while the
remaining 11 (92%) reacted, either by looking at the helicopter (n=10)
or by departing from their basking site (n=1). Blackwell et al. (2004a)
concluded that none of the reactions to helicopters were strong or long
lasting, and that seals near Northstar in June and July 2000 probably
had habituated to industrial sounds and visible activities that had
occurred often during the preceding winter and spring. There have been
few
[[Page 19262]]
systematic studies of pinniped reactions to aircraft overflights, and
most of the available data concern pinnipeds hauled out on land or ice
rather than pinnipeds in the water (Richardson et al., 1995a; Born et
al., 1999).
Reactions of harbor seals to the simulated sound of a 2-megawatt
wind power generator were measured by Koschinski et al. (2003). Harbor
seals surfaced significantly further away from the sound source when it
was active and did not approach the sound source as closely. The device
used in that study produced sounds in the frequency range of 30 to 800
Hz, with peak source levels of 128 dB at 1 m at the 80- and 160-Hz
frequencies.
Pinnipeds are not likely to show a strong avoidance reaction to the
airgun sources proposed for use. Visual monitoring from seismic vessels
has shown only slight (if any) avoidance of airguns by pinnipeds and
only slight (if any) changes in behavior. Monitoring work in the
Alaskan Beaufort Sea during 1996-2001 provided considerable information
regarding the behavior of Arctic ice seals exposed to seismic pulses
(Harris et al., 2001; Moulton and Lawson, 2002). These seismic projects
usually involved arrays of 6 to 16 airguns with total volumes of 560 to
1,500 in\3\. The combined results suggest that some seals avoid the
immediate area around seismic vessels. In most survey years, ringed
seal sightings tended to be farther away from the seismic vessel when
the airguns were operating than when they were not (Moulton and Lawson,
2002). However, these avoidance movements were relatively small, on the
order of 100 m (328 ft) to a few hundreds of meters, and many seals
remained within 100-200 m (328-656 ft) of the trackline as the
operating airgun array passed by. Seal sighting rates at the water
surface were lower during airgun array operations than during no-airgun
periods in each survey year except 1997. Similarly, seals are often
very tolerant of pulsed sounds from seal-scaring devices (Mate and
Harvey, 1987; Jefferson and Curry, 1994; Richardson et al., 1995a).
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 the species occurring in the present study area are as
strong as those evident in the telemetry study, reactions are expected
to be confined to relatively small distances and durations, with no
long-term effects on pinniped individuals or populations.
4. Threshold Shift (Noise-Induced Loss of Hearing)
When animals exhibit reduced hearing sensitivity (i.e., sounds must
be louder for an animal to detect them) following exposure to an
intense sound or sound for long duration, it is referred to as a noise-
induced threshold shift (TS). An animal can experience temporary
threshold shift (TTS) or permanent threshold shift (PTS). TTS can last
from minutes or hours to days (i.e., there is complete recovery), can
occur in specific frequency ranges (i.e., an animal might only have a
temporary loss of hearing sensitivity between the frequencies of 1 and
10 kHz), and can be of varying amounts (for example, an animal's
hearing sensitivity might be reduced initially by only 6 dB or reduced
by 30 dB). PTS is permanent, but some recovery is possible. PTS can
also occur in a specific frequency range and amount as mentioned above
for TTS.
The following physiological mechanisms are thought to play a role
in inducing auditory TS: Effects to sensory hair cells in the inner ear
that reduce their sensitivity, modification of the chemical environment
within the sensory cells, residual muscular activity in the middle ear,
displacement of certain inner ear membranes, increased blood flow, and
post-stimulatory reduction in both efferent and sensory neural output
(Southall et al., 2007). The amplitude, duration, frequency, temporal
pattern, and energy distribution of sound exposure all can affect the
amount of associated TS and the frequency range in which it occurs. As
amplitude and duration of sound exposure increase, so, generally, does
the amount of TS, along with the recovery time. For intermittent
sounds, less TS could occur than compared to a continuous exposure with
the same energy (some recovery could occur between intermittent
exposures depending on the duty cycle between sounds) (Kryter et al.,
1966; Ward, 1997). For example, one short but loud (higher SPL) sound
exposure may induce the same impairment as one longer but softer sound,
which in turn may cause more impairment than a series of several
intermittent softer sounds with the same total energy (Ward, 1997).
Additionally, though TTS is temporary, prolonged exposure to sounds
strong enough to elicit TTS, or shorter-term exposure to sound levels
well above the TTS threshold, can cause PTS, at least in terrestrial
mammals (Kryter, 1985). However, in the case of the proposed
exploratory drilling program, animals are not expected to be exposed to
levels high enough or durations long enough to result in PTS.
PTS is considered auditory injury (Southall et al., 2007).
Irreparable damage to the inner or outer cochlear hair cells may cause
PTS; however, other mechanisms are also involved, such as exceeding the
elastic limits of certain tissues and membranes in the middle and inner
ears and resultant changes in the chemical composition of the inner ear
fluids (Southall et al., 2007).
Although the published body of scientific literature contains
numerous theoretical studies and discussion papers on hearing
impairments that can occur with exposure to a loud sound, only a few
studies provide empirical information on the levels at which noise-
induced loss in hearing sensitivity occurs in nonhuman animals. For
marine mammals, published data are limited to the captive bottlenose
dolphin, beluga, harbor porpoise, and Yangtze finless porpoise
(Finneran et al., 2000, 2002b, 2003, 2005a, 2007, 2010a, 2010b;
Finneran and Schlundt, 2010; Lucke et al., 2009; Mooney et al., 2009a,
2009b; Popov et al., 2011a, 2011b; Kastelein et al., 2012a; Schlundt et
al., 2000; Nachtigall et al., 2003, 2004). For pinnipeds in water, data
are limited to measurements of TTS in harbor seals, an elephant seal,
and California sea lions (Kastak et al., 1999, 2005; Kastelein et al.,
2012b).
Marine mammal hearing plays a critical role in communication with
conspecifics, and interpretation of environmental cues for purposes
such as predator avoidance and prey capture. Depending on the degree
(elevation of threshold in dB), duration (i.e., recovery time), and
frequency range of TTS, and the context in which it is experienced, TTS
can have effects on marine mammals ranging from discountable to serious
(similar to those discussed in auditory masking, below). For example, a
marine mammal may be able to readily compensate for a brief, relatively
small amount of TTS in a non-critical frequency range that occurs
during a time where ambient noise is lower and there are not as many
competing sounds present. Alternatively, a larger amount and longer
duration of TTS sustained during time when communication is critical
for successful mother/calf interactions could have more serious
impacts. Also, depending on the degree and frequency range, the effects
of PTS on an animal could range in severity, although it is considered
generally more serious because it is a permanent condition. Of note,
reduced hearing sensitivity as a simple function of aging has been
observed in marine mammals,
[[Page 19263]]
as well as humans and other taxa (Southall et al., 2007), so we can
infer that strategies exist for coping with this condition to some
degree, though likely not without cost.
Given the higher level of sound necessary to cause PTS as compared
with TTS, it is considerably less likely that PTS would occur during
the proposed exploratory drilling program in Cook Inlet. However,
several of the sound sources do not even emit sound levels at levels
high enough to potentially even cause TTS.
5. Non-Auditory Physical Effects
Non-auditory physical effects might occur in marine mammals exposed
to strong underwater 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, and other types of organ or tissue damage.
Some marine mammal species (i.e., beaked whales) may be especially
susceptible to injury and/or stranding when exposed to strong pulsed
sounds.
Classic stress responses begin when an animal's central nervous
system perceives a potential threat to its homeostasis. That perception
triggers stress responses regardless of whether a stimulus actually
threatens the animal; the mere perception of a threat is sufficient to
trigger a stress response (Moberg, 2000; Sapolsky et al., 2005; Seyle,
1950). Once an animal's central nervous system perceives a threat, it
mounts a biological response or defense that consists of a combination
of the four general biological defense responses: Behavioral responses;
autonomic nervous system responses; neuroendocrine responses; or immune
responses.
In the case of many stressors, an animal's first and most
economical (in terms of biotic costs) response is behavioral avoidance
of the potential stressor or avoidance of continued exposure to a
stressor. An animal's second line of defense to stressors involves the
sympathetic part of the autonomic nervous system and the classical
``fight or flight'' response, which includes the cardiovascular system,
the gastrointestinal system, the exocrine glands, and the adrenal
medulla to produce changes in heart rate, blood pressure, and
gastrointestinal activity that humans commonly associate with
``stress.'' These responses have a relatively short duration and may or
may not have significant long-term effects on an animal's welfare.
An animal's third line of defense to stressors involves its
neuroendocrine or sympathetic nervous systems; the system that has
received the most study has been the hypothalmus-pituitary-adrenal
system (also known as the HPA axis in mammals or the hypothalamus-
pituitary-interrenal axis in fish and some reptiles). Unlike stress
responses associated with the autonomic nervous system, virtually all
neuroendocrine functions that are affected by stress--including immune
competence, reproduction, metabolism, and behavior--are regulated by
pituitary hormones. Stress-induced changes in the secretion of
pituitary hormones have been implicated in failed reproduction (Moberg,
1987; Rivier, 1995), altered metabolism (Elasser et al., 2000), reduced
immune competence (Blecha, 2000), and behavioral disturbance. Increases
in the circulation of glucocorticosteroids (cortisol, corticosterone,
and aldosterone in marine mammals; see Romano et al., 2004) have been
equated with stress for many years.
The primary distinction between stress (which is adaptive and does
not normally place an animal at risk) and distress is the biotic cost
of the response. During a stress response, an animal uses glycogen
stores that can be quickly replenished once the stress is alleviated.
In such circumstances, the cost of the stress response would not pose a
risk to the animal's welfare. However, when an animal does not have
sufficient energy reserves to satisfy the energetic costs of a stress
response, energy resources must be diverted from other biotic
functions, which impair those functions that experience the diversion.
For example, when mounting a stress response diverts energy away from
growth in young animals, those animals may experience stunted growth.
When mounting a stress response diverts energy from a fetus, an
animal's reproductive success and fitness will suffer. In these cases,
the animals will have entered a pre-pathological or pathological state
which is called ``distress'' (sensu Seyle, 1950) or ``allostatic
loading'' (sensu McEwen and Wingfield, 2003). This pathological state
will last until the animal replenishes its biotic reserves sufficient
to restore normal function. Note that these examples involved a long-
term (days or weeks) stress response exposure to stimuli.
Relationships between these physiological mechanisms, animal
behavior, and the costs of stress responses have also been documented
fairly well through controlled experiment; because this physiology
exists in every vertebrate that has been studied, it is not surprising
that stress responses and their costs have been documented in both
laboratory and free-living animals (for examples see, Holberton et al.,
1996; Hood et al., 1998; Jessop et al., 2003; Krausman et al., 2004;
Lankford et al., 2005; Reneerkens et al., 2002; Thompson and Hamer,
2000). Although no information has been collected on the physiological
responses of marine mammals to anthropogenic sound exposure, studies of
other marine animals and terrestrial animals would lead us to expect
some marine mammals to experience physiological stress responses and,
perhaps, physiological responses that would be classified as
``distress'' upon exposure to anthropogenic sounds.
For example, Jansen (1998) reported on the relationship between
acoustic exposures and physiological responses that are indicative of
stress responses in humans (e.g., elevated respiration and increased
heart rates). Jones (1998) reported on reductions in human performance
when faced with acute, repetitive exposures to acoustic disturbance.
Trimper et al. (1998) reported on the physiological stress responses of
osprey to low-level aircraft noise while Krausman et al. (2004)
reported on the auditory and physiology stress responses of endangered
Sonoran pronghorn to military overflights. Smith et al. (2004a, 2004b)
identified noise-induced physiological transient stress responses in
hearing-specialist fish (i.e., goldfish) that accompanied short- and
long-term hearing losses. Welch and Welch (1970) reported physiological
and behavioral stress responses that accompanied damage to the inner
ears of fish and several mammals.
Hearing is one of the primary senses marine mammals use to gather
information about their environment and communicate with conspecifics.
Although empirical information on the relationship between sensory
impairment (TTS, PTS, and acoustic masking) on marine mammals remains
limited, we assume that reducing a marine mammal's ability to gather
information about its environment and communicate with other members of
its species would induce stress, based on data that terrestrial animals
exhibit those responses under similar conditions (NRC, 2003) and
because marine mammals use hearing as their primary sensory mechanism.
Therefore, we assume that acoustic exposures sufficient to trigger
onset PTS or TTS would be accompanied by physiological stress
responses. Marine mammals might experience stress responses at received
levels lower than those necessary to trigger onset TTS. Based on
empirical studies of the time required to
[[Page 19264]]
recover from stress responses (Moberg, 2000), NMFS also assumes that
stress responses could persist beyond the time interval required for
animals to recover from TTS and might result in pathological and pre-
pathological states that would be as significant as behavioral
responses to TTS. However, as stated previously in this document, the
source level of the jack-up rig is not loud enough to induce PTS or
likely even TTS.
Resonance effects (Gentry, 2002) and direct noise-induced bubble
formations (Crum et al., 2005) are implausible in the case of exposure
to an impulsive broadband source like an airgun array. If seismic
surveys disrupt diving patterns of deep-diving species, this might
result in bubble formation and a form of the bends, as speculated to
occur in beaked whales exposed to sonar. However, there is no specific
evidence of this upon exposure to airgun pulses. Additionally, no
beaked whale species occur in the proposed project area.
In general, very little is known about the potential for strong,
anthropogenic underwater sounds to cause non-auditory physical effects
in marine mammals. Such effects, if they occur at all, would presumably
be limited to short distances and to activities that extend over a
prolonged period. The available data do not allow identification of a
specific exposure level above which non-auditory effects can be
expected (Southall et al., 2007) or any meaningful quantitative
predictions of the numbers (if any) of marine mammals that might be
affected in those ways. There is no definitive evidence that any of
these effects occur even for marine mammals in close proximity to large
arrays of airguns, which are not proposed for use during this program.
For the most part, only low-level continuous sounds would be produced
during the exploratory drilling program. In addition, marine mammals
that show behavioral avoidance of industry activities, including
belugas and some pinnipeds, are especially unlikely to incur non-
auditory impairment or other physical effects.
6. Stranding and Mortality
Marine mammals close to underwater detonations of high explosive
can be killed or severely injured, and the auditory organs are
especially susceptible to injury (Ketten et al., 1993; Ketten, 1995).
Airgun pulses are less energetic and their peak amplitudes have slower
rise times. To date, there is no evidence that serious injury, death,
or stranding by marine mammals can occur from exposure to airgun
pulses, even in the case of large airgun arrays. Additionally, the
airguns used during VSP are used for short periods of time. The
continuous sounds produced by the drill rig are also far less
energetic.
It should be noted that strandings related to sound exposure have
not been recorded for marine mammal species in Cook Inlet. Beluga whale
strandings in Cook Inlet are not uncommon; however, these events often
coincide with extreme tidal fluctuations (``spring tides'') or killer
whale sightings (Shelden et al., 2003). For example, in August 2012, a
group of Cook Inlet beluga whales stranded in the mud flats of
Turnagain Arm during low tide and were able to swim free with the flood
tide. NMFS does not expect any marine mammals will incur serious injury
or mortality in Cook Inlet or strand as a result of the proposed
exploratory drilling program.
Vessel Impacts
Vessel activity and noise associated with vessel activity will
temporarily increase in the action area during Buccaneer's exploratory
drilling program as a result of the operation of a jack-up drill rig
and the use of tow and other support vessels. While under tow, the rig
and the tow vessels move at slow speeds (2-4 knots). The support barges
supplying pipe to the drill rig can typically run at 7-8 knots but may
move slower inside Cook Inlet. Based on this information, NMFS does not
anticipate and does not propose to authorize take from vessel strikes.
Odontocetes, such as beluga whales, killer whales, and harbor
porpoises, often show tolerance to vessel activity; however, they may
react at long distances if they are confined by ice, shallow water, or
were previously harassed by vessels (Richardson et al., 1995). Beluga
whale response to vessel noise varies greatly from tolerance to extreme
sensitivity depending on the activity of the whale and previous
experience with vessels (Richardson et al., 1995). Reactions to vessels
depends on whale activities and experience, habitat, boat type, and
boat behavior (Richardson et al., 1995) and may include behavioral
responses, such as altered headings or avoidance (Blane and Jaakson,
1994; Erbe and Farmer, 2000); fast swimming; changes in vocalizations
(Lesage et al., 1999; Scheifele et al., 2005); and changes in dive,
surfacing, and respiration patterns.
There are few data published on pinniped responses to vessel
activity, and most of the information is anecdotal (Richardson et al.,
1995). Generally, sea lions in water show tolerance to close and
frequently approaching vessels and sometimes show interest in fishing
vessels. They are less tolerant when hauled out on land; however, they
rarely react unless the vessel approaches within 100-200 m (330-660 ft;
reviewed in Richardson et al., 1995).
The addition of the jack-up rig and a few support vessels and noise
due to rig and vessel operations associated with the exploratory
drilling program would not be outside the present experience of marine
mammals in Cook Inlet, although levels may increase locally. Given the
large number of vessels in Cook Inlet and the apparent habituation to
vessels by Cook Inlet marine mammals that may occur in the area, vessel
activity and noise is not expected to have effects that could cause
significant or long-term consequences for individual marine mammals or
their populations.
Oil Spill and Discharge Impacts
As noted above, the specified activity involves the drilling of
exploratory wells and associated activities in upper Cook Inlet during
the 2014 open water season. The primary stressors to marine mammals
that are reasonably expected to occur will be acoustic in nature. The
likelihood of a large or very large oil spill occurring during
Buccaneer's proposed exploratory drilling program is remote. Offshore
oil spill records in Cook Inlet during 1994-2011 show three spills
during oil exploration (ADNR Division of Oil and Gas, 2011 unpub.
data): Two oil spills at the UNOCAL Dillion Platform in June 2011 (two
gallons) and December 2001 (three gallons); and one oil spill at the
UNOCAL Monopod Platform in January 2002 (one gallon). During this same
time period, 71 spills occurred offshore in Cook Inlet during oil
production. Most spills ranged from 0.0011 to 1 gallon (42 spills), and
only three spills were larger than 200 gallons: 210 gallons in July
2001 at the Cook Inlet Energy Stewart facility; 250 gallons in February
1998 at the King Salmon platform; and 504 gallons in October 1999 at
the UNOCAL Dillion platform. All 71 crude oil spills from the offshore
platforms, both exploration and production, totaled less than 2,140
gallons. Based on historical data, most oil spills have been small.
Moreover, during more than 60 years of oil and gas exploration and
development in Cook Inlet, there has not been a single oil well
blowout, making it difficult to assign a specific risk factor to the
possibility of such an event in Cook Inlet. However, the probability of
such an event is thought to be of extremely low probability.
[[Page 19265]]
Buccaneer will have various measures and protocols in place that
will be implemented to prevent oil releases from the wellbore.
Buccaneer has planned formal routine rig maintenance and surveillance
checks, as well as normal inspection and equipment checks to be
conducted on the jack-up rig daily. The following steps will be in
place to prevent oil from entering the water:
Required inspections will follow standard operating
procedures.
Personnel working on the rig will be directed to report
any unusual conditions to appropriate personnel.
Oily equipment will be regularly wiped down with oil
absorbent pads to collect free oil. Drips and small spillage from
equipment will be controlled through use of drip pans and oil absorbent
drop clothes.
Oil absorbent materials used to contain oil spills or
seeps will be collected and disposed of in sealed plastic bags or metal
drums and closed containers.
The platform surfaces will be kept clean of waste
materials and loose debris on a daily basis.
Remedial actions will be taken when visual inspections
indicate deterioration of equipment (tanks) and/or their control
systems.
Following remedial work, and as appropriate, tests will be
conducted to determine that the systems function correctly.
Drilling and completion fluids provide primary well control during
drilling, work over, or completion operations. These fluids are
designed to exert hydrostatic pressure on the wellbore that exceeds the
pore pressures within the subsurface formations. This prevents
undesired fluid flow into the wellbore. Surface mounted blowout
preventer (BOP) equipment provides secondary well control. In the event
that primary well control is lost, this surface equipment is used to
contain the influx of formation fluid and then safely circulate it out
of the wellbore.
The BOP is a large, specialized valve used to seal, control, and
monitor oil and gas wells. BOPs come in variety of styles, sizes, and
pressure ratings. For Cook Inlet, the BOP equipment used by Buccaneer
will consist of:
Three BOPs pressure safety levels of: (1) 5,000 pounds per
square inch (psi) (2) 10,000 psi, and (3) 15,000 psi;
A minimum of three 35 cm (13 \5/8\ in), 10,000 psi WP ram
type preventers;
One 35 cm (13 \5/8\ in) annular preventer;
Choke and kill lines that provide circulating paths from/
to the choke manifold;
A two choke manifold that allows for safe circulation of
well influxes out of the well bore; and
A hydraulic control system with accumulator backup
closing.
The wellhead, associated valves, and control systems provide
blowout prevention during well production. These systems provide
several layers of redundancy to ensure pressure containment is
maintained. Well control planning is performed in accordance with
Alaska Oil and Gas Conservation Commission (AOGCC) and Bureau of Safety
and Environment Enforcement (BSEE) regulations. The operator's policies
and recommended practices are, at a minimum, equivalent to BSEE
regulations. BOP test drills are performed on a frequent basis to
ensure the well will be shut in quickly and properly. BOP testing
procedures will meet American Petroleum Institute Recommended Practice
No. 53 and AOGCC specifications. The BOP tests will be conducted with a
nonfreezing fluid when the ambient temperature around the BOP stack is
below 0 [deg]C (32 [deg]F). Tests will be conducted at least weekly and
before drilling out the shoe of each casing string. The AOGCC will be
contacted before each test is conducted, and will be onsite during BOP
tests unless an inspection waiver is approved.
Buccaneer developed an Oil Discharge Prevention and Contingency
Plan (ODPCP). Alaska's Department of Environmental Conservation (ADEC)
approved Buccaneer's ODPCP on August 29, 2012. NMFS reviewed the ODPCP
during the ESA consultation process and found that with implementation
of the safety features mentioned above that the risk of an oil spill
was discountable.
Despite concluding that the risk of serious injury or mortality
from an oil spill in this case is extremely remote, NMFS has
nonetheless evaluated the potential effects of an oil spill on marine
mammals. While an oil spill is not a component of Buccaneer's specified
activity for which NMFS is proposing to authorize take, potential
impacts on marine mammals from an oil spill are discussed in more
detail next.
1. Potential Effects of Oil on Cetaceans
The specific effects an oil spill would have on cetaceans are not
well known. While mortality is unlikely, exposure to spilled oil could
lead to skin irritation, baleen fouling (which might reduce feeding
efficiency), respiratory distress from inhalation of hydrocarbon
vapors, consumption of some contaminated prey items, and temporary
displacement from contaminated feeding areas. Geraci and St. Aubin
(1990) summarize effects of oil on marine mammals. The number of
cetaceans that might be contacted by a spill would depend on the size,
timing, and duration of the spill and where the oil is in relation to
the animals. Whales may not avoid oil spills, and some have been
observed feeding within oil slicks (Goodale et al., 1981).
There is no direct evidence that oil spills, including the much
studied Santa Barbara Channel and Exxon Valdez spills, have caused any
deaths of cetaceans (Geraci, 1990; Brownell, 1971; Harvey and Dahlheim,
1994). It is suspected that some individually identified killer whales
that disappeared from Prince William Sound during the time of the Exxon
Valdez spill were casualties of that spill. However, no clear cause and
effect relationship between the spill and the disappearance could be
established (Dahlheim and Matkin, 1994). The AT-1 pod of transient
killer whales that sometimes inhabits Prince William Sound has
continued to decline after the Exxon Valdez oil spill (EVOS). Matkin et
al. (2008) tracked the AB resident pod and the AT-1 transient group of
killer whales from 1984 to 2005. The results of their photographic
surveillance indicate a much higher than usual mortality rate for both
populations the year following the spill (33% for AB Pod and 41% for
AT-1 Group) and lower than average rates of increase in the 16 years
after the spill (annual increase of about 1.6% for AB Pod compared to
an annual increase of about 3.2% for other Alaska killer whale pods).
In killer whale pods, mortality rates are usually higher for non-
reproductive animals and very low for reproductive animals and
adolescents (Olesiuk et al., 1990, 2005; Matkin et al., 2005). No
effects on humpback whales in Prince William Sound were evident after
the EVOS (von Ziegesar et al., 1994). There was some temporary
displacement of humpback whales out of Prince William Sound, but this
could have been caused by oil contamination, boat and aircraft
disturbance, displacement of food sources, or other causes.
Migrating gray whales were apparently not greatly affected by the
Santa Barbara spill of 1969. There appeared to be no relationship
between the spill and mortality of marine mammals. The higher than
usual counts of dead marine mammals recorded after the spill
represented increased survey effort and therefore cannot be
conclusively linked to the spill itself (Brownell, 1971; Geraci, 1990).
The conclusion was that whales were either
[[Page 19266]]
able to detect the oil and avoid it or were unaffected by it (Geraci,
1990).
Schwake et al. (2013) studied two populations of common bottlenose
dolphins in the Gulf of Mexico following the Deepwater Horizon oil
spill to evaluate sublethal effects. They conducted health assessments
in Barataria Bay, Louisiana, an area that received heavy and prolonged
oiling and in a reference site, Sarasota Bay, Florida, where oil was
not observed. Several disease conditions were noted for the Barataria
Bay dolphins, including hypoadrenocorticism, pulmonary abnormalities,
and tooth loss (Schwake et al., 2013). Even though several of the
observed health effects are consistent with exposure to petroleum
hydrocarbons because the researchers did not have prespill health data
for the Barataria Bay dolphins, they cannot rule out that other pre-
existing environmental stressors made this population particularly
vulnerable to effects from the oil spill (Schwake et al., 2013).
Whales rely on a layer of blubber for insulation, so oil would have
little if any effect on thermoregulation by whales. Effects of oiling
on cetacean skin appear to be minor and of little significance to the
animal's health (Geraci, 1990). Histological data and ultrastructural
studies by Geraci and St. Aubin (1990) showed that exposures of skin to
crude oil for up to 45 minutes in four species of toothed whales had no
effect. They switched to gasoline and applied the sponge up to 75
minutes. This produced transient damage to epidermal cells in whales.
Subtle changes were evident only at the cell level. In each case, the
skin damage healed within a week. They concluded that a cetacean's skin
is an effective barrier to the noxious substances in petroleum. These
substances normally damage skin by getting between cells and dissolving
protective lipids. In cetacean skin, however, tight intercellular
bridges, vital surface cells, and the extraordinary thickness of the
epidermis impeded the damage. The authors could not detect a change in
lipid concentration between and within cells after exposing skin from a
white-sided dolphin to gasoline for 16 hours in vitro.
Whales could ingest oil if their food is contaminated, or oil could
also be absorbed through the respiratory tract. Some of the ingested
oil is voided in vomit or feces but some is absorbed and could cause
toxic effects (Geraci, 1990). When returned to clean water,
contaminated animals can depurate this internal oil (Engelhardt, 1978,
1982). Oil ingestion can decrease food assimilation of prey eaten (St.
Aubin, 1988). Cetaceans may swallow some oil-contaminated prey, but it
likely would be only a small part of their food. It is not known if
whales would leave a feeding area where prey was abundant following a
spill. Some zooplankton eaten by baleen whales consume oil particles,
and bioaccumulation can result. Tissue studies by Geraci and St. Aubin
(1990) revealed low levels of naphthalene in the livers and blubber of
baleen whales. This result suggests that prey have low concentrations
in their tissues, or that baleen whales may be able to metabolize and
excrete certain petroleum hydrocarbons. However, baleen whale species
are uncommon in the location of Buccaneer's proposed well sites. Baleen
whales are more likely to be encountered in the lower Inlet during rig
towing, far away from the drill sites. Whales exposed to an oil spill
are unlikely to ingest enough oil to cause serious internal damage
(Geraci and St. Aubin, 1980, 1982), and this kind of damage has not
been reported (Geraci, 1990).
Some cetaceans can detect oil and sometimes avoid it, but others
enter and swim through slicks without apparent effects (Geraci, 1990;
Harvey and Dahlheim, 1994). Bottlenose dolphins in the Gulf of Mexico
apparently could detect and avoid slicks and mousse but did not avoid
light sheens on the surface (Smultea and Wursig, 1995). After the Regal
Sword spill in 1979, various species of baleen and toothed whales were
observed swimming and feeding in areas containing spilled oil southeast
of Cape Cod, MA (Goodale et al., 1981). For months following EVOS,
there were numerous observations of gray whales, harbor porpoises,
Dall's porpoises, and killer whales swimming through light-to-heavy
crude-oil sheens (Harvey and Dalheim, 1994, cited in Matkin et al.,
2008). However, if some of the animals avoid the area because of the
oil, then the effects of the oiling would be less severe on those
individuals.
2. Potential Effects of Oil on Pinnipeds
Externally oiled phocid seals often survive and become clean, but
heavily oiled seal pups and adults may die, depending on the extent of
oiling and characteristics of the oil. Adult seals may suffer some
temporary adverse effects, such as eye and skin irritation, with
possible infection (MMS, 1996). Such effects may increase stress, which
could contribute to the death of some individuals. There is a
likelihood that newborn seal pups, if contacted by oil, would die from
oiling through loss of insulation and resulting hypothermia.
Reports of the effects of oil spills have shown that some mortality
of seals may have occurred as a result of oil fouling; however, large
scale mortality had not been observed prior to the EVOS (St. Aubin,
1990). Effects of oil on marine mammals were not well studied at most
spills because of lack of baseline data and/or the brevity of the post-
spill surveys. The largest documented impact of a spill, prior to EVOS,
was on young seals in January in the Gulf of St. Lawrence (St. Aubin,
1990). Brownell and Le Boeuf (1971) found no marked effects of oil from
the Santa Barbara oil spill on California sea lions or on the mortality
rates of newborn pups.
Intensive and long-term studies were conducted after the EVOS in
Alaska. There may have been a long-term decline of 36% in numbers of
molting harbor seals at oiled haul-out sites in Prince William Sound
following EVOS (Frost et al., 1994a). However, in a reanalysis of those
data and additional years of surveys, along with an examination of
assumptions and biases associated with the original data, Hoover-Miller
et al. (2001) concluded that the EVOS effect had been overestimated.
The decline in attendance at some oiled sites was more likely a
continuation of the general decline in harbor seal abundance in Prince
William Sound documented since 1984 (Frost et al., 1999) rather than a
result of EVOS. The results from Hoover-Miller et al. (2001) indicate
that the effects of EVOS were largely indistinguishable from natural
decline by 1992. However, while Frost et al. (2004) concluded that
there was no evidence that seals were displaced from oiled sites, they
did find that aerial counts indicated 26% fewer pups were produced at
oiled locations in 1989 than would have been expected without the oil
spill. Harbor seal pup mortality at oiled beaches was 23% to 26%, which
may have been higher than natural mortality, although no baseline data
for pup mortality existed prior to EVOS (Frost et al., 1994a). There
was no conclusive evidence of spill effects on Steller sea lions
(Calkins et al., 1994). Oil did not persist on sea lions themselves (as
it did on harbor seals), nor did it persist on sea lion haul-out sites
and rookeries (Calkins et al., 1994). Sea lion rookeries and haul out
sites, unlike those used by harbor seals, have steep sides and are
subject to high wave energy (Calkins et al., 1994).
Adult seals rely on a layer of blubber for insulation, and oiling
of the external surface does not appear to have adverse
thermoregulatory effects (Kooyman et al., 1976, 1977; St. Aubin, 1990).
Contact with oil on the external surfaces
[[Page 19267]]
can potentially cause increased stress and irritation of the eyes of
ringed seals (Geraci and Smith, 1976; St. Aubin, 1990). These effects
seemed to be temporary and reversible, but continued exposure of eyes
to oil could cause permanent damage (St. Aubin, 1990). Corneal ulcers
and abrasions, conjunctivitis, and swollen nictitating membranes were
observed in captive ringed seals placed in crude oil-covered water
(Geraci and Smith, 1976) and in seals in the Antarctic after an oil
spill (Lillie, 1954).
Marine mammals can ingest oil if their food is contaminated. Oil
can also be absorbed through the respiratory tract (Geraci and Smith,
1976; Engelhardt et al., 1977). Some of the ingested oil is voided in
vomit or feces but some is absorbed and could cause toxic effects
(Engelhardt, 1981). When returned to clean water, contaminated animals
can depurate this internal oil (Engelhardt, 1978, 1982, 1985). In
addition, seals exposed to an oil spill are unlikely to ingest enough
oil to cause serious internal damage (Geraci and St. Aubin, 1980,
1982).
Although seals may have the capability to detect and avoid oil,
they apparently do so only to a limited extent (St. Aubin, 1990). Seals
may abandon the area of an oil spill because of human disturbance
associated with cleanup efforts, but they are most likely to remain in
the area of the spill. One notable behavioral reaction to oiling is
that oiled seals are reluctant to enter the water, even when intense
cleanup activities are conducted nearby (St. Aubin, 1990; Frost et al.,
1994b, 2004).
Seals that are under natural stress, such as lack of food or a
heavy infestation by parasites, could potentially die because of the
additional stress of oiling (Geraci and Smith, 1976; St. Aubin, 1990;
Spraker et al., 1994). Female seals that are nursing young would be
under natural stress, as would molting seals. In both cases, the seals
would have reduced food stores and may be less resistant to effects of
oil than seals that are not under some type of natural stress. Seals
that are not under natural stress (e.g., fasting, molting) would be
more likely to survive oiling. In general, seals do not exhibit large
behavioral or physiological reactions to limited surface oiling or
incidental exposure to contaminated food or vapors (St. Aubin, 1990;
Williams et al., 1994). Effects could be severe if seals surface in
heavy oil slicks in leads or if oil accumulates near haul-out sites
(St. Aubin, 1990).
Anticipated Effects on Marine Mammal Habitat
The primary potential impacts to marine mammals and other marine
species are associated with elevated sound levels produced by the
exploratory drilling program (i.e. the drill rig and the airguns).
However, other potential impacts are also possible to the surrounding
habitat from physical disturbance, discharges, and an oil spill (should
one occur). This section describes the potential impacts to marine
mammal habitat from the specified activity. Because the marine mammals
in the area feed on fish and/or invertebrates there is also information
on the species typically preyed upon by the marine mammals in the area.
Common Marine Mammal Prey in the Proposed Drilling Area
Fish are the primary prey species for marine mammals in upper Cook
Inlet. Beluga whales feed on a variety of fish, shrimp, squid, and
octopus (Burns and Seaman, 1986). Common prey species in Knik Arm
include salmon, eulachon and cod. Harbor seals feed on fish such as
pollock, cod, capelin, eulachon, Pacific herring, and salmon, as well
as a variety of benthic species, including crabs, shrimp, and
cephalopods. Harbor seals are also opportunistic feeders with their
diet varying with season and location. The preferred diet of the harbor
seal in the Gulf of Alaska consists of pollock, octopus, capelin,
eulachon, and Pacific herring (Calkins, 1989). Other prey species
include cod, flat fishes, shrimp, salmon, and squid (Hoover, 1988).
Harbor porpoises feed primarily on Pacific herring, cod, whiting
(hake), pollock, squid, and octopus (Leatherwood et al., 1982). In the
upper Cook Inlet area, harbor porpoise feed on squid and a variety of
small schooling fish, which would likely include Pacific herring and
eulachon (Bowen and Siniff, 1999; NMFS, unpublished data). Killer
whales feed on either fish or other marine mammals depending on genetic
type (resident versus transient respectively). Killer whales in Knik
Arm are typically the transient type (Shelden et al., 2003) and feed on
beluga whales and other marine mammals, such as harbor seal and harbor
porpoise. The Steller sea lion diet consists of a variety of fishes
(capelin, cod, herring, mackerel, pollock, rockfish, salmon, sand
lance, etc.), bivalves, squid, octopus, and gastropods.
Potential Impacts From Seafloor Disturbance on Marine Mammal Habitat
There is a possibility of seafloor disturbance or increased
turbidity in the vicinity of the drill sites. Seafloor disturbance
could occur with bottom founding of the drill rig legs and anchoring
system. These activities could lead to direct effects on bottom fauna,
through either displacement or mortality. Increase in suspended
sediments from seafloor disturbance also has the potential to
indirectly affect bottom fauna and fish. The amount and duration of
disturbed or turbid conditions will depend on sediment material.
The potential direct habitat impact by the Buccaneer drilling
operation is limited to the actual drill-rig footprint defined as the
area occupied and enclosed by the drill-rig legs. The jack-up rig will
temporarily disturb up to two offshore locations in upper Cook Inlet,
where the wells are proposed to be drilled. Bottom disturbance would
occur in the area where the three legs of the rig would be set down and
where the actual well would be drilled. The jack-up drill rig footprint
would occupy three steel piles at 14 m (46 ft) diameter. The well
casing would be a 76 cm (30 in) diameter pipe extending from the
seafloor to the rig floor. The casing would only be in place during
drilling activities at each potential well location. The total area of
disturbance was calculated as 0.54 acres during the land use permitting
process. The collective 2-acre footprint of the wells represents a very
small fraction of the 7,300 square mile Cook Inlet surface area.
Potential damage to the Cook Inlet benthic community will be limited to
the actual surface area of the three spud cans (1,585 square feet each
or 4,755 square feet total) that form the ``foot'' of each leg. Given
the high tidal energy at the well site locations, drilling footprints
are not expected to support benthic communities equivalent to shallow
lower energy sites found in nearshore waters where harbor seals mostly
feed. The presence of the drill rig is not expected to result in direct
loss of marine mammal habitat.
Potential Impacts From Sound Generation
With regard to fish as a prey source for odontocetes and seals,
fish are known to hear and react to sounds and to use sound to
communicate (Tavolga et al., 1981) and possibly avoid predators (Wilson
and Dill, 2002). Experiments have shown that fish can sense both the
strength and direction of sound (Hawkins, 1981). Primary factors
[[Page 19268]]
determining whether a fish can sense a sound signal, and potentially
react to it, are the frequency of the signal and the strength of the
signal in relation to the natural background noise level.
Fishes produce sounds that are associated with behaviors that
include territoriality, mate search, courtship, and aggression. It has
also been speculated that sound production may provide the means for
long distance communication and communication under poor underwater
visibility conditions (Zelick et al., 1999), although the fact that
fish communicate at low-frequency sound levels where the masking
effects of ambient noise are naturally highest suggests that very long
distance communication would rarely be possible. Fishes have evolved a
diversity of sound generating organs and acoustic signals of various
temporal and spectral contents. Fish sounds vary in structure,
depending on the mechanism used to produce them (Hawkins, 1993).
Generally, fish sounds are predominantly composed of low frequencies
(less than 3 kHz).
Since objects in the water scatter sound, fish are able to detect
these objects through monitoring the ambient noise. Therefore, fish are
probably able to detect prey, predators, conspecifics, and physical
features by listening to environmental sounds (Hawkins, 1981). There
are two sensory systems that enable fish to monitor the vibration-based
information of their surroundings. The two sensory systems, the inner
ear and the lateral line, constitute the acoustico-lateralis system.
Although the hearing sensitivities of very few fish species have
been studied to date, it is becoming obvious that the intra- and inter-
specific variability is considerable (Coombs, 1981). Nedwell et al.
(2004) compiled and published available fish audiogram information. A
noninvasive electrophysiological recording method known as auditory
brainstem response is now commonly used in the production of fish
audiograms (Yan, 2004). Generally, most fish have their best hearing in
the low-frequency range (i.e., less than 1 kHz). Even though some fish
are able to detect sounds in the ultrasonic frequency range, the
thresholds at these higher frequencies tend to be considerably higher
than those at the lower end of the auditory frequency range.
Literature relating to the impacts of sound on marine fish species
can be divided into the following categories: (1) Pathological effects;
(2) physiological effects; and (3) behavioral effects. Pathological
effects include lethal and sub-lethal physical damage to fish;
physiological effects include primary and secondary stress responses;
and behavioral effects include changes in exhibited behaviors of fish.
Behavioral changes might be a direct reaction to a detected sound or a
result of the anthropogenic sound masking natural sounds that the fish
normally detect and to which they respond. The three types of effects
are often interrelated in complex ways. For example, some physiological
and behavioral effects could potentially lead to the ultimate
pathological effect of mortality. Hastings and Popper (2005) reviewed
what is known about the effects of sound on fishes and identified
studies needed to address areas of uncertainty relative to measurement
of sound and the responses of fishes. Popper et al. (2003/2004) also
published a paper that reviews the effects of anthropogenic sound on
the behavior and physiology of fishes.
Potential effects of exposure to continuous sound on marine fish
include TTS, physical damage to the ear region, physiological stress
responses, and behavioral responses such as startle response, alarm
response, avoidance, and perhaps lack of response due to masking of
acoustic cues. Most of these effects appear to be either temporary or
intermittent and therefore probably do not significantly impact the
fish at a population level. The studies that resulted in physical
damage to the fish ears used noise exposure levels and durations that
were far more extreme than would be encountered under conditions
similar to those expected during Buccaneer's proposed exploratory
drilling activities.
The level of sound at which a fish will react or alter its behavior
is usually well above the detection level. Fish have been found to
react to sounds when the sound level increased to about 20 dB above the
detection level of 120 dB (Ona, 1988); however, the response threshold
can depend on the time of year and the fish's physiological condition
(Engas et al., 1993). In general, fish react more strongly to pulses of
sound rather than a continuous signal (Blaxter et al., 1981), such as
the type of sound that will be produced by the drillship, and a quicker
alarm response is elicited when the sound signal intensity rises
rapidly compared to sound rising more slowly to the same level.
Investigations of fish behavior in relation to vessel noise (Olsen
et al., 1983; Ona, 1988; Ona and Godo, 1990) have shown that fish react
when the sound from the engines and propeller exceeds a certain level.
Avoidance reactions have been observed in fish such as cod and herring
when vessels approached close enough that received sound levels are 110
dB to 130 dB (Nakken, 1992; Olsen, 1979; Ona and Godo, 1990; Ona and
Toresen, 1988). However, other researchers have found that fish such as
polar cod, herring, and capeline are often attracted to vessels
(apparently by the noise) and swim toward the vessel (Rostad et al.,
2006). Typical sound source levels of vessel noise in the audible range
for fish are 150 dB to 170 dB (Richardson et al., 1995a). (Based on
models, the 160 dB radius for the jack-up rig would extend
approximately 33 ft [10 m]; therefore, fish would need to be in close
proximity to the drill rig for the noise to be audible). In calm
weather, ambient noise levels in audible parts of the spectrum lie
between 60 dB to 100 dB.
Buccaneer also proposes to conduct VSP surveys with an airgun array
for a short period of time during the drilling season (only a few hours
over 1-2 days per well over the course of the entire proposed drilling
program). Airguns produce impulsive sounds as opposed to continuous
sounds at the source. Short, sharp sounds can cause overt or subtle
changes in fish behavior. Chapman and Hawkins (1969) tested the
reactions of whiting (hake) in the field to an airgun. When the airgun
was fired, the fish dove from 82 to 180 ft (25 to 55 m) depth and
formed a compact layer. The whiting dove when received sound levels
were higher than 178 dB re 1 [mu]Pa (Pearson et al., 1992).
Pearson et al. (1992) conducted a controlled experiment to
determine effects of strong noise pulses on several species of rockfish
off the California coast. They used an airgun with a source level of
223 dB re 1 [micro]Pa. They noted:
Startle responses at received levels of 200-205 dB re 1
[mu]Pa and above for two sensitive species, but not for two other
species exposed to levels up to 207 dB;
Alarm responses at 177-180 dB for the two sensitive
species, and at 186 to 199 dB for other species;
An overall threshold for the above behavioral response at
about 180 dB;
An extrapolated threshold of about 161 dB for subtle
changes in the behavior of rockfish; and
A return to pre-exposure behaviors within the 20-60 minute
exposure period.
In summary, fish often react to sounds, especially strong and/or
intermittent sounds of low frequency. Sound pulses at received levels
of 160 dB re 1 [mu]Pa may cause subtle changes in behavior. Pulses at
levels of 180 dB may cause noticeable changes in behavior (Chapman and
Hawkins, 1969;
[[Page 19269]]
Pearson et al., 1992; Skalski et al., 1992). It also appears that fish
often habituate to repeated strong sounds rather rapidly, on time
scales of minutes to an hour. However, the habituation does not endure,
and resumption of the strong sound source may again elicit disturbance
responses from the same fish. Underwater sound levels from the drill
rig and other vessels produce sounds lower than the response threshold
reported by Pearson et al. (1992), and are not likely to result in
major effects to fish near the proposed drill sites.
Based on a sound level of approximately 140 dB, there may be some
avoidance by fish of the area near the jack-up while drilling, around
the rig under tow, and around other support and supply vessels when
underway. Any reactions by fish to these sounds will last only minutes
(Mitson and Knudsen, 2003; Ona et al., 2007) longer than the vessel is
operating at that location or the drill rig is drilling. Any potential
reactions by fish would be limited to a relatively small area within
about 33 ft (10 m) of the drill rig during drilling. Avoidance by some
fish or fish species could occur within portions of this area.
The lease areas do not support major populations of cod, Pollock,
and sole, although all four salmon species and smelt migrate through
the area to spawning rivers in upper Cook Inlet (Shields and Dupuis,
2012). Residency time for the migrating finfish in the vicinity of an
operating platform would be short-term, limiting fish exposure to noise
associated with the proposed drilling program.
Some of the fish species found in Cook Inlet are prey sources for
odontocetes and pinnipeds. A reaction by fish to sounds produced by
Buccaneer's proposed operations would only be relevant to marine
mammals if it caused concentrations of fish to vacate the area.
Pressure changes of sufficient magnitude to cause that type of reaction
would probably occur only very close to the sound source, if any would
occur at all due to the low energy sounds produced by the majority of
equipment proposed for use. Impacts on fish behavior are predicted to
be inconsequential. Thus, feeding odontocetes and pinnipeds would not
be adversely affected by this minimal loss or scattering, if any, which
is not expected to result in reduced prey abundance. The proposed
drilling area is not a common feeding area for baleen whales.
Potential Impacts From Drilling Discharges
The drill rig Endeavour will operate under the Alaska Pollutant
Discharge Elimination System (APDES) general permit AKG-31-5021 for
wastewater discharges (ADEC, 2012). This permit authorizes discharges
from oil and gas extraction facilities engaged in exploration under the
Offshore and Coastal Subcategories of the Oil and Gas Extraction Point
Source Category (40 CFR Part 435). Twelve effluents are authorized for
discharge into Cook Inlet once ADEC discharge limits have been met. The
authorized discharges include: Drilling fluids and drill cuttings, deck
drainage, sanitary waste, domestic waste, blowout preventer fluid,
boiler blow down, fire control system test water, uncontaminated
ballast water, bilge water, excess cement slurry, mud cuttings cement
at sea floor, and completion fluids. Areas prohibited from discharge in
the Cook Inlet are 10-meter (33-foot) isobaths, 5-meter (16-foot)
isobaths, and other geographic area restrictions (AKG-31-5021.I.C.).
The Endeavour is also authorized under EPA's Vessel General Permit for
deck wash down and runoff, gray water, and gray water mixed with sewage
discharges. The effluent limits and related requirements for these
discharges in the Vessel General Permit are to minimize or eliminate to
the extent achievable using control measures (best management
practices) (EPA, 2011).
Drilling wastes include drilling fluids, known as mud, rock
cuttings, and formation waters. Drilling wastes (non-hydrocarbon) will
be discharged to the Cook Inlet under the approved APDES general
permit. Drilling wastes (hydrocarbon) will be delivered to an onshore
permitted location for disposal. During drilling, the onsite tool
pusher/driller and qualified mud engineers will direct and maintain
desired mud properties, and maintain the quantities of basic mud
materials on site as dictated by good oilfield practice. Buccaneer will
follow best management practices to ensure that a sufficient inventory
of barite and lost circulation materials are maintained on the drilling
vessel to minimize the possibility of a well upset and the likelihood
of a release of pollutants to Cook Inlet waters. These materials can be
re-supplied, if required, using the supply vessel. Because adverse
weather could prevent immediate re-supply, sufficient materials will be
available on board to completely rebuild the total circulating volume.
Buccaneer will conduct an Environmental Monitoring Study of relevant
hydrographic, sediment hydrocarbon, and heavy metal data from surveys
conducted before and during drilling mud disposal and up to a least one
year after drilling operations cease in accordance with the APDES
general permit for discharges of drilling muds and cuttings.
Non-drilling wastewater includes deck drainage, sanitary waste,
domestic waste, blowout preventer fluid, boiler blow down, fire control
test water, bilge water, non-contact cooling water, and uncontaminated
ballast water. Non-drilling wastewater will be discharged into Cook
Inlet under the approved APDES general permit or delivered to an
onshore permitted location for disposal. Mud cuttings will be
constantly tested. No hydrocarboned muds will be permitted to be
discharged into Cook Inlet. They will be hauled offsite. Solid waste
(e.g., packaging, domestic trash) will be classified, segregated, and
labeled as general, universal, and Resource Conservation and Recovery
Act exempt or non-exempt waste. It will be stored in containers at
designated accumulation areas. Then, it will be packaged and palletized
for transport to an approved on-shore disposal facility. No hazardous
wastes should not be generated as a result of this project. However, if
any hazardous wastes were generated, it would be temporarily stored in
an onboard satellite accumulation area and then transported offsite for
disposal at an approved facility.
With oil and gas platforms presently operating in Cook Inlet, there
is concern for continuous exposure to potentially toxic heavy metals
and metalloids (i.e., mercury, lead, cadmium, copper, zinc, and
arsenic) that are associated with oil and gas development and
production. These elements occur naturally in the earths' crust and the
oceans but many also have anthropogenic origins from local sources of
pollution or from contamination from atmospheric distribution.
Discharging drill cuttings or other liquid waste streams generated
by the drilling vessel could potentially affect marine mammal habitat.
Toxins could persist in the water column, which could have an impact on
marine mammal prey species. However, despite a considerable amount of
investment in research on exposures of marine mammals to
organochlorines or other toxins, there have been no marine mammal
deaths in the wild that can be conclusively linked to the direct
exposure to such substances (O'Shea, 1999).
Drilling muds and cuttings discharged to the seafloor can lead to
localized
[[Page 19270]]
increased turbidity and increase in background concentrations of barium
and occasionally other metals in sediments and may affect lower trophic
organisms. Drilling muds are composed primarily of bentonite (clay),
and the toxicity is therefore low. Heavy metals in the mud may be
absorbed by benthic organisms, but studies have shown that heavy metals
do not bio-magnify in marine food webs (Neff et al., 1989). Effects on
benthic communities are nearly always restricted to a zone within about
328 to 492 ft (100 to 150 m) of the discharge, where cuttings
accumulations are greatest. Discharges and drill cuttings could impact
fish by displacing them from the affected area.
Beluga whales analyzed for heavy metals and other elements
(cadmium, mercury, selenium, vanadium, and silver) were generally lower
in the livers of Cook Inlet animals than in the other beluga whale
stocks, while copper was higher (Becker et al., 2001). Hepatic methyl
mercury levels were similar to those reported for other beluga whales
(Geraci and St. Aubin, 1990). The relatively high hepatic concentration
of silver found in the eastern Chukchi Sea and Beaufort Sea stocks of
belugas was also found in the Cook Inlet animals, suggesting a species-
specific phenomenon. However, because of the limited discharges no
water quality impacts are anticipated that would negatively affect
habitat for Cook Inlet marine mammals.
Potential Impacts From Drill Rig Presence
The horizontal dimensions of the jack-up rig are 160 ft by 35 ft
(48.8 m by 10.7 m). The dimensions of the drill rig (less than one
football field on either side) are not significant enough to cause a
large-scale diversion from the animals' normal swim and migratory
paths. Any deflection of marine mammal species due to the physical
presence of the drill rig would be very minor. The drill rig's physical
footprint is small relative to the size of the geographic region it
will occupy and will likely not cause marine mammals to deflect greatly
from their typical migratory route. Also, even if animals may deflect
because of the presence of the drill rig, Cook Inlet is much larger in
size than the length of the drill rig (many dozens of miles vs. less
than one football field), and animals would have other means of passage
around the drill rig. In sum, the physical presence of the drill rig is
not likely to cause a significant deflection to migrating marine
mammals.
Potential Impacts From an Oil Spill
Lower trophic organisms and fish species are primary food sources
for marine mammals likely to be found in the proposed project vicinity.
Any diminishment of feeding habitat during the summer months due to an
oil spill or response could affect the energy balance of marine
mammals. If oil found its way into upper Cook Inlet in the area of the
Susitna and Little Susitna rivers during the summer months, a large
portion of Cook Inlet beluga whale Area 1 critical habitat could be
impacted. If an oil spill were to occur later in the season, it could
become trapped in or under the ice or travel with the thinner ice pans.
Due to their wide distribution, large numbers, and rapid rate of
regeneration, the recovery of marine invertebrate populations is
expected to occur soon after the surface oil passes. Spill response
activities are not likely to disturb the prey items of whales or seals
sufficiently to cause more than minor effects. Spill response
activities could cause marine mammals to avoid the disturbed habitat
that is being cleaned. However, by causing avoidance, animals would
avoid impacts from the oil itself. Additionally, the likelihood of an
oil spill is expected to be very low, as discussed earlier in this
document.
Based on the preceding discussion of potential types of impacts to
marine mammal habitat, overall, the proposed specified activity is not
expected to cause significant impacts on habitats used by the marine
mammal species in the proposed project area or on the food sources that
they utilize.
Proposed Mitigation
In order to issue an incidental take authorization (ITA) under
section 101(a)(5)(D) of the MMPA, NMFS must set forth the permissible
methods of taking pursuant to such activity, and other means of
effecting the least practicable impact on such species or stock and its
habitat, paying particular attention to rookeries, mating grounds, and
areas of similar significance, and on the availability of such species
or stock for taking for certain subsistence uses (where relevant).
Later in this document in the ``Proposed Incidental Harassment
Authorization'' section, NMFS lays out the proposed conditions for
review, as they would appear in the final IHA (if issued).
While the drill rig does not emit sound levels that require
shutdowns to avoid Level A harassment (injury), because take of beluga
whales is not authorized, shutdown procedures will be required to avoid
Level B take of this species. For continuous sounds, such as those
produced by drilling operations and rig tow, NMFS uses a received level
of 120-dB (rms) to indicate the onset of Level B harassment. For
impulse sounds, such as those produced by the airgun array during the
VSP surveys or the impact hammer during conductor pipe driving, NMFS
uses a received level of 160-dB (rms) to indicate the onset of Level B
harassment. The current Level A (injury) harassment threshold is 180 dB
(rms) for cetaceans and 190 dB (rms) for pinnipeds. Table 1 in this
document outlines the various applicable radii for which different
mitigation measures would apply.
Table 1--Applicable Mitigation and Shutdown Radii for Buccaneer's Proposed Upper Cook Inlet Exploratory Drilling Program
--------------------------------------------------------------------------------------------------------------------------------------------------------
190 dB radius 180 dB radius 160 dB radius 120 dB radius
--------------------------------------------------------------------------------------------------------------------------------------------------------
Impact hammer during conductor pipe 60 m (200 ft).............. 250 m (820 ft)............. 2 km (1.24 mi)............. NA.
driving.
Airguns during VSP.................. 75 m (246 ft).............. 240 m (787 ft)............. 2.5 km (1.55 mi)........... NA.
Rig tow............................. NA......................... NA......................... NA......................... 600 m (2,000 ft).
Deep well pumps on the jack-up rig.. NA......................... NA......................... NA......................... 260 m (853 ft).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Rig tow source levels do not exceed 171 dB (rms); Jack-up rig source levels without deep well pumps is below ambient sound levels; NA = Not applicable.
[[Page 19271]]
Mitigation Measures Proposed by Buccaneer
For the proposed mitigation measures, Buccaneer listed the
following protocols to be implemented during its exploratory drilling
program in Cook Inlet.
1. Conductor Pipe Driving Measures
Protected species observers (PSOs) will observe from the drill rig
during this 2-3 day portion of the proposed program out to the 160 dB
(rms) radius of 2 km (1.24 mi). If marine mammal species for which take
is not authorized enter this zone, then use of the impact hammer will
cease. If cetaceans for which take is authorized enter within the 180
dB (rms) radius of 250 m (820 ft) or if pinnipeds for which take is
authorized enter within the 190 dB (rms) radius of 60 m (200 ft), then
use of the impact hammer will cease. Following a shutdown of impact
hammering activities, the applicable zones must be clear of marine
mammals for at least 30 minutes prior to restarting activities.
Buccaneer proposes to follow a ramp-up procedure during impact
hammering activities. PSOs will visually monitor out to the 160 dB
radius for at least 30 minutes prior to the initiation of activities.
If no marine mammals are detected during that time, then Buccaneer can
initiate impact hammering using a ``soft start'' technique. Hammering
will begin with an initial set of three strikes at 40 percent energy
followed by a 1 min waiting period, then two subsequent three-strike
sets. This ``soft-start'' procedure will be implemented anytime impact
hammering has ceased for 30 minutes or more. Impact hammer ``soft-
start'' will not be required if the hammering downtime is for less than
30 minutes and visuals surveys are continued throughout the silent
period and no marine mammals are observed in the applicable zones
during that time. Monitoring will occur during all hammering sessions.
2. VSP Airgun Measures
PSOs will observe from the drill rig during this 1-2 day portion of
the proposed program out to the 160 dB radius of 2.5 km (1.55 mi). If
marine mammal species for which take is not authorized enter this zone,
then use of the airguns will cease. If cetaceans for which take is
authorized enter within the 180 dB (rms) radius of 240 m (787 ft) or if
pinnipeds for which take is authorized enter within the 190 dB (rms)
radius of 75 m (246 ft), then use of the airguns will cease. Following
a shutdown of airgun operations, the applicable zones must be clear of
marine mammals for at least 30 minutes prior to restarting activities.
Buccaneer proposes to follow a ramp-up procedure during airgun
operations. PSOs will visually monitor out to the 160 dB radius for at
least 30 minutes prior to the initiation of activities. If no marine
mammals are detected during that time, then Buccaneer can initiate
airgun operations using a ``ramp-up'' technique. Airgun operations will
begin with the firing of a single airgun, which will be the smallest
gun in the array in terms of energy output (dB) and volume (in\3\).
Operators will then continue ramp-up by gradually activating additional
airguns over a period of at least 30 minutes (but not longer than 40
minutes) until the desired operating level of the airgun array is
obtained. This ramp-up procedure will be implemented anytime airguns
have not been fired for 30 minutes or more. Airgun ramp-up will not be
required if the airguns have been off for less than 30 minutes and
visuals surveys are continued throughout the silent period and no
marine mammals are observed in the applicable zones during that time.
Monitoring will occur during all airgun usage.
3. Rig Tow and Drill Rig Operation
As mentioned previously, these activities do not generate sounds
that require implementation of mitigation measures to avoid injury.
However, PSOs will be stationed on the helicopter platform (bow) of the
drill rig (positioned about 100 ft above the waterline) to watch for
marine mammals. With the exception of the operation of the deep-well
pump on the jack-up rig, the other machinery generates sound levels
below ambient. PSOs will observe from the drill rig during this portion
of the proposed program out to the 120 dB radius of 260 m (853 ft). If
marine mammal species for which take is not authorized enter this zone,
then the deep well pumps will be turned off. The PSOs will operate from
multiple stations on the rig, recognizing that the shutdown radius
begins from the submersed pump housed inside the forward jack-up leg.
4. Oil Spill Plan
Buccaneer developed an ODPCP. ADEC approved Buccaneer's ODPCP on
August 29, 2012. NMFS reviewed the ODPCP during the ESA consultation
process and found that with implementation of the safety features
mentioned above that the risk of an oil spill was discountable.
5. Pollution Discharge Plan
When the drill rig is towed or otherwise floating it is classified
as a vessel (like a barge). During those periods, it is covered under a
form of National Pollutant Discharge Elimination System permit known as
a Vessel General Permit. This permit remains federal and is a ``no
discharge permit,'' which allows for the discharge of storm water and
closed system fire suppression water but no other effluents.
When the legs are down, the drill rig becomes a facility. During
those periods, it is covered under an approved APDES. Under the APDES,
certain discharges are permitted. However, Buccaneer is not permitted
to discharge gray water, black water, or hydrocarboned muds. They are
all hauled off and not discharged.
Mitigation Measures Proposed by NMFS
NMFS proposes that when Buccaneer utilizes helicopters for support
operations that the helicopters must maintain an altitude of at least
1,000 ft (305 m), except during takeoffs, landings, or emergency
situations.
Mitigation Conclusions
NMFS has carefully evaluated Buccaneer's proposed mitigation
measures and considered a range of other measures in the context of
ensuring that NMFS prescribes the means of effecting the least
practicable impact on the affected marine mammal species and stocks and
their habitat. Our evaluation of potential measures included
consideration of the following factors in relation to one another:
The manner in which, and the degree to which, the
successful implementation of the measures are expected to minimize
adverse impacts to marine mammals;
The proven or likely efficacy of the specific measure to
minimize adverse impacts as planned; and
The practicability of the measure for applicant
implementation.
Any mitigation measure(s) prescribed by NMFS should be able to
accomplish, have a reasonable likelihood of accomplishing (based on
current science), or contribute to the accomplishment of one or more of
the general goals listed below:
1. Avoidance or minimization of injury or death of marine mammals
wherever possible (goals 2, 3, and 4 may contribute to this goal).
2. A reduction in the numbers of marine mammals (total number or
number at biologically important time or location) exposed to received
levels
[[Page 19272]]
of seismic airguns, impact hammers, drill rig deep well pumps, or other
activities expected to result in the take of marine mammals (this goal
may contribute to 1, above, or to reducing harassment takes only).
3. A reduction in the number of times (total number or number at
biologically important time or location) individuals would be exposed
to received levels of seismic airguns impact hammers, drill rig deep
well pumps, or other activities expected to result in the take of
marine mammals (this goal may contribute to 1, above, or to reducing
harassment takes only).
4. A reduction in the intensity of exposures (either total number
or number at biologically important time or location) to received
levels of seismic airguns impact hammers, drill rig deep well pumps, or
other activities expected to result in the take of marine mammals (this
goal may contribute to 1, above, or to reducing the severity of
harassment takes only).
5. Avoidance or minimization of adverse effects to marine mammal
habitat, paying special attention to the food base, activities that
block or limit passage to or from biologically important areas,
permanent destruction of habitat, or temporary destruction/disturbance
of habitat during a biologically important time.
6. For monitoring directly related to mitigation--an increase in
the probability of detecting marine mammals, thus allowing for more
effective implementation of the mitigation.
Based on our evaluation of the applicant's proposed measures, as
well as other measures considered by NMFS, NMFS has preliminarily
determined that the proposed mitigation measures provide the means of
effecting the least practicable impact on marine mammals species or
stocks and their habitat, paying particular attention to rookeries,
mating grounds, and areas of similar significance.
Proposed Monitoring and Reporting
In order to issue an ITA for an activity, section 101(a)(5)(D) of
the MMPA states that NMFS must set forth ``requirements pertaining to
the monitoring and reporting of such taking''. The MMPA implementing
regulations at 50 CFR 216.104 (a)(13) indicate that requests for ITAs
must include the suggested means of accomplishing the necessary
monitoring and reporting that will result in increased knowledge of the
species and of the level of taking or impacts on populations of marine
mammals that are expected to be present in the proposed action area.
Buccaneer submitted information regarding marine mammal monitoring to
be conducted during seismic operations as part of the IHA application.
That information can be found in Appendix C of the application. The
monitoring measures may be modified or supplemented based on comments
or new information received from the public during the public comment
period.
Monitoring measures proposed by the applicant or prescribed by NMFS
should accomplish one or more of the following top-level goals:
1. An increase in our understanding of the likely occurrence of
marine mammal species in the vicinity of the action, i.e., presence,
abundance, distribution, and/or density of species.
2. An increase in our understanding of the nature, scope, or
context of the likely exposure of marine mammal species to any of the
potential stressor(s) associated with the action (e.g. sound or visual
stimuli), through better understanding of one or more of the following:
The action itself and its environment (e.g. sound source
characterization, propagation, and ambient noise levels); the affected
species (e.g. life history or dive pattern); the likely co-occurrence
of marine mammal species with the action (in whole or part) associated
with specific adverse effects; and/or the likely biological or
behavioral context of exposure to the stressor for the marine mammal
(e.g. age class of exposed animals or known pupping, calving or feeding
areas).
3. An increase in our understanding of how individual marine
mammals respond (behaviorally or physiologically) to the specific
stressors associated with the action (in specific contexts, where
possible, e.g., at what distance or received level).
4. An increase in our understanding of how anticipated individual
responses, to individual stressors or anticipated combinations of
stressors, may impact either: The long-term fitness and survival of an
individual; or the population, species, or stock (e.g. through effects
on annual rates of recruitment or survival).
5. An increase in our understanding of how the activity affects
marine mammal habitat, such as through effects on prey sources or
acoustic habitat (e.g., through characterization of longer-term
contributions of multiple sound sources to rising ambient noise levels
and assessment of the potential chronic effects on marine mammals).
6. An increase in understanding of the impacts of the activity on
marine mammals in combination with the impacts of other anthropogenic
activities or natural factors occurring in the region.
7. An increase in our understanding of the effectiveness of
mitigation and monitoring measures.
8. An increase in the probability of detecting marine mammals
(through improved technology or methodology), both specifically within
the safety zone (thus allowing for more effective implementation of the
mitigation) and in general, to better achieve the above goals.
Proposed Monitoring Measures
1. Visual Monitoring
PSOs will be required to monitor the area for marine mammals aboard
the drill rig during rig tow, exploratory drilling operations,
conductor pipe driving, and VSP operations. Standard marine mammal
observing field equipment will be used, including reticule binoculars,
Big-eye binoculars, inclinometers, and range-finders. If conductor pipe
driving or VSP operations occur at night, PSOs will be equipped with
night scopes. At least one PSO will be on duty at all times when
operations are occurring. Shifts shall not last more than 4 hours, and
PSOs will not observe for more than 12 hours in a 24-hour period.
2. Sound Source Verification Monitoring
A sound source verification (SSV) of the underwater sound pressures
emanating from the active drilling rig will be conducted by an
acoustical engineer. The measurements would be made in a boat that is
drifting near the rig in the current. Measuring while drifting will
minimize the noise contamination caused by strumming of the hydrophone
lines and flow noise. Measurements will be made with a two-channel
system that will provide measurements at two specified depths up to 100
feet. The underwater sound levels would be measured using hydrophones,
sound level meters, and recording devices.
Measurements would be made by hydrophones that have a flat
frequency response and are omnidirectional over a frequency range of 10
to 20,000 Hz. The signals shall be fed into an appropriate date-logging
device, such as an integrating sound level meter. The systems will have
the capability to make quality recordings using a digital audio
recorder (either solid state or tape). The accuracy of the measurement
system shall be 1 dB from 10 to 10,000 Hz referenced to 1 micro Pascal
([mu]Pa). The measurement system shall be able to
[[Page 19273]]
measure the unweighted or C-weighted root-mean-square (rms) sound
pressure levels in dB referenced to 1 [mu]Pa. The measurement systems
will have the capability to provide a real time readout display of
underwater sound levels. The real-time display shall provide the
unweighted peak sound pressure and the sound pressure level. During
drilling, measurements were made out to beyond the 120 dB isopleth.
During any other activity (e.g., conductor driving and VSP operations),
measurements were or will be made to at least one kilometer from the
rig. To date, SSVs have been conducted for drilling operations,
generators, submersed pumps, and VSP operations (I&R, 2013a, b, c). SSV
of the conductor pipe driving activity is planned to occur.
Recordings of sounds will be conducted so that subsequent analysis
could be provided and certain sounds could be identified or at least
described. The subsequent analysis would include providing frequency
spectra for different sounds or distances from the rig. The spectra
data would be provided in \1/3\rd octave bands for sounds in the 10 to
10,000 Hz range.
In addition to the underwater sound measurements, measurements of
sea temperature, wind speed, and sea state will be (or were) taken as
well.
Reporting Measures
1. SSV Report
The SSV report will describe the source of the sound, the
environment, the measurements, and the methodology employed to make the
measurements. Results will be presented as overall sound pressure
levels and displays of 1/3rd octave band sound levels. Preliminary
findings relative to the 120 dB, 160 dB, 180 dB, and 190 dB isopleths
will be provided within 1 week of SSV completion.
2. 90-Day Technical Report
Daily field reports will be prepared that include daily activities,
marine mammal monitoring efforts, and a record of the marine mammals
and their behaviors and reactions observed that day. These daily
reports will be used to help generate the 90-day technical report. A
report will be due to NMFS no later than 90 days after the expiration
of the IHA (if issued). The Technical Report will include the
following:
Summaries of monitoring effort (e.g., total hours, total
distances, and marine mammal distribution through the study period,
accounting for sea state and other factors affecting visibility and
detectability of marine mammals).
Analyses of the effects of various factors influencing
detectability of marine mammals (e.g., sea state, number of observers,
and fog/glare).
Species composition, occurrence, and distribution of
marine mammal sightings, including date, water depth, numbers, age/
size/gender categories (if determinable), group sizes, and ice cover.
Analyses of the effects of operations.
Sighting rates of marine mammals (and other variables that
could affect detectability), such as: (i) Initial sighting distances
versus operational activity state; (ii) closest point of approach
versus operational activity state; (iii) observed behaviors and types
of movements versus operational activity state; (iv) numbers of
sightings/individuals seen versus operational activity state; (v)
distribution around the drill rig versus operational activity state;
and (vi) estimates of take by Level B harassment based on presence in
the Level B harassment zones.
3. Notification of Injured or Dead Marine Mammals
In the unanticipated event that the specified activity clearly
causes the take of a marine mammal in a manner prohibited by the IHA
(if issued), such as an injury (Level A harassment), serious injury or
mortality (e.g., ship-strike, gear interaction, and/or entanglement),
Buccaneer would immediately cease the specified activities and
immediately report the incident to the Chief of the Permits and
Conservation Division, Office of Protected Resources, NMFS, and the
Alaska Regional Stranding Coordinators. The report would include the
following information:
Time, date, and location (latitude/longitude) of the
incident;
Name and type of vessel involved;
Vessel's speed during and leading up to the incident;
Description of the incident;
Status of all sound source use in the 24 hours preceding
the incident;
Water depth;
Environmental conditions (e.g., wind speed and direction,
Beaufort sea state, cloud cover, and visibility);
Description of all marine mammal observations in the 24
hours preceding the incident;
Species identification or description of the animal(s)
involved;
Fate of the animal(s); and
Photographs or video footage of the animal(s) (if
equipment is available).
Activities would not resume until NMFS is able to review the
circumstances of the prohibited take. NMFS would work with Buccaneer to
determine what is necessary to minimize the likelihood of further
prohibited take and ensure MMPA compliance. Buccaneer would not be able
to resume their activities until notified by NMFS via letter, email, or
telephone.
In the event that Buccaneer discovers an injured or dead marine
mammal, and the lead PSO determines that the cause of the injury or
death is unknown and the death is relatively recent (i.e., in less than
a moderate state of decomposition as described in the next paragraph),
Buccaneer would immediately report the incident to the Chief of the
Permits and Conservation Division, Office of Protected Resources, NMFS,
and the NMFS Alaska Stranding Hotline and/or by email to the Alaska
Regional Stranding Coordinators. The report would include the same
information identified in the paragraph above. Activities would be able
to continue while NMFS reviews the circumstances of the incident. NMFS
would work with Buccaneer to determine whether modifications in the
activities are appropriate.
In the event that Buccaneer discovers an injured or dead marine
mammal, and the lead PSO determines that the injury or death is not
associated with or related to the activities authorized in the IHA
(e.g., previously wounded animal, carcass with moderate to advanced
decomposition, or scavenger damage), Buccaneer would report the
incident to the Chief of the Permits and Conservation Division, Office
of Protected Resources, NMFS, and the NMFS Alaska Stranding Hotline
and/or by email to the Alaska Regional Stranding Coordinators, within
24 hours of the discovery. Buccaneer would provide photographs or video
footage (if available) or other documentation of the stranded animal
sighting to NMFS and the Marine Mammal Stranding Network.
Estimated Take by Incidental Harassment
Except with respect to certain activities not pertinent here, the
MMPA defines ``harassment'' as: any act of pursuit, torment, or
annoyance which (i) has the potential to injure a marine mammal or
marine mammal stock in the wild [Level A harassment]; or (ii) has the
potential to disturb a marine mammal or marine mammal stock in the wild
by causing disruption of behavioral patterns, including, but not
limited to, migration, breathing, nursing, breeding, feeding, or
sheltering [Level B harassment]. Only take by Level B behavioral
harassment of some species
[[Page 19274]]
is anticipated as a result of the proposed drilling program.
Anticipated impacts to marine mammals are associated with noise
propagation from the sound sources (e.g., drill rig and tow, airguns,
and impact hammer) used in the drilling program. Additional disturbance
to marine mammals may result from visual disturbance of the drill rig
or support vessels. No take is expected to result from vessel strikes
because of the slow speed of the vessels (2-4 knots while rig is under
two; 7-8 knots of supply barges).
Buccaneer requests authorization to take six marine mammal species
by Level B harassment. These six marine mammal species are: Gray whale;
minke whale; killer whale; harbor porpoise; Dall's porpoise; and harbor
seal. Take of Cook Inlet beluga whales is not requested, expected, or
proposed to be authorized. NMFS Section 7 ESA biologists concluded that
Buccaneer's proposed exploratory drilling program is not likely to
adversely affect Cook Inlet beluga whales. Mitigation measures
requiring shutdowns of activities before belugas enter the Level B
harassment zones will be required in any issued IHA.
As noted previously in this document, for continuous sounds, such
as those produced by drilling operations and rig tow, NMFS uses a
received level of 120-dB (rms) to indicate the onset of Level B
harassment. For impulse sounds, such as those produced by the airgun
array during the VSP surveys or the impact hammer during conductor pipe
driving, NMFS uses a received level of 160-dB (rms) to indicate the
onset of Level B harassment. The current Level A (injury) harassment
threshold is 180 dB (rms) for cetaceans and 190 dB (rms) for pinnipeds.
Table 2 outlines the current acoustic criteria.
Table 2--Current Acoustic Exposure Criteria Used by NMFS
------------------------------------------------------------------------
Criterion Criterion definition Threshold
------------------------------------------------------------------------
Level A Harassment (injury). Permanent Threshold 180 dB re 1 microPa-
Shift (PTS). m (cetaceans)/190
(Any level above dB re 1 microPa-m
that which is known (pinnipeds) root
to cause TTS). mean square (rms).
Level B Harassment.......... Behavioral 160 dB re 1 microPa-
Disruption. m (rms).
(for impulse noises)
Level B Harassment.......... Behavioral 120 dB re 1 microPa-
Disruption. m (rms).
(for continuous,
noise).
------------------------------------------------------------------------
Section 6 of Buccaneer's application contains a description of the
methodology used by Buccaneer to estimate takes by harassment,
including calculations for the 120 dB (rms) and 160 dB (rms) isopleths
and marine mammal densities in the areas of operation (see ADDRESSES),
which is also provided in the following sections. NMFS verified
Buccaneer's methods, and used the density and sound isopleth
measurements in estimating take. However, NMFS also include a duration
factor in the estimates presented below, which is not included in
Buccaneer's application.
Simply, the proposed take estimates presented in this section for
harbor porpoise and harbor seal were calculated by multiplying summer
density for the species (which constitutes the best available density
information) by the area of ensonification for each type of activity by
the total number of days that each activity would occur. For the other
four species (minke, gray, and killer whales and Dall's porpoise),
there are no available density estimates because of their low
occurrence rates in Cook Inlet. Therefore, take requests for those
species are based on opportunistic sightings data and typical group
size for each species. Additional detail is provided next.
Ensonified Areas
1. Rig Tow
The jack-up rig will be towed three times during 2014. It is
estimated that the longer tows will take 2 days to complete. The rig
will be wet-towed by at least two ocean-going tugs licensed to operate
in Cook Inlet. Tugs generate their loudest sounds while towing due to
propeller cavitation. While these continuous sounds have been measured
at up to 171 dB re 1 [mu]Pa-m (rms) at source (broadband), they are
generally emitted at dominant frequencies of less than 5 kHz (Miles et
al., 1987; Richardson et al., 1995; Simmonds et al., 2004).
For the most part, the dominant noise frequencies from propeller
cavitation are less than the dominant hearing frequencies for pinnipeds
and toothed whales. Because it is currently unknown which tug or tugs
will be used to tow the rig, and there are few sound signatures for
tugs in general, the potential area that could be ensonified by
disturbance-level noise is calculated based on an assumed 171 dB re 1
[mu]Pa-m source. Using Collins et al.'s (2007) 171--18.4 Log(R)--
0.00188 spreading model determine from hydroacoustic surveys in Cook
Inlet, the distance to the 120 dB isopleth would be at 1,715 ft (523
m). The associated ZOI (area ensonified by noise greater than 120 dB)
is, therefore, 212 acres (0.86 km\2\).
2. Conductor Pipe Driving
The Delmar D62-22 diesel impact hammer proposed to be used by
Buccaneer to drive the 30-inch conductor pipe was previously
acoustically measured by Blackwell (2005) in upper Cook Inlet. She
found that sound exceeding 190 dB Level A noise limits for pinnipeds
extend to about 200 feet (60 meters), and 180 dB Level A impacts to
cetaceans to about 820 feet (250 meters). Level B disturbance levels of
160 dB extended to just less than 1.2 miles (1.9 kilometers). The
associated ZOI (area ensonified by noise greater than 160 dB) is 4.4
mi\2\ (11.3 km\2\).
3. Deep-Well Pumps (Jack-Up Rig)
Buccaneer proposes to use the jack-up drilling rig Endeavour for
the Cook Inlet program. Because the drilling platform and other noise-
generating equipment on a jack-up rig are located above the sea's
surface, and there is very little surface contact with the water
compared to drill ships and semisubmersible drill rigs, lattice-legged
jack-up drill rigs are relatively quiet (Richardson et al., 1995;
Spence et al., 2007).
The Spartan 151, the only other jack-up drill rig currently
operating in the Cook Inlet, was hydroacoustically measured by Marine
Acoustics, Inc. (2011) in 2011. The survey results showed that
continuous noise levels exceeding 120 dB re 1 [mu]Pa extended out only
50 m (164 ft), and that this noise was largely associated with the
diesel engines used as hotel power generators, rather than the drilling
table. Similar, or lesser, noise levels were expected to be generated
by the Endeavour because generators are mounted on pedestals
specifically to reduce noise transfer through the infrastructure, and
enclosed
[[Page 19275]]
in an insulated engine room, with the intent of reducing underwater
noise transmission to levels even lower than the Spartan 151. This was
confirmed during an SSV test on the Endeavour by Illingworth and Rodkin
(2013a) in May 2013 where it was determined that the noise levels
associated with drilling and operating generators are below ambient.
However, the SSV identified another sound source, the submersed
deep-well pumps, which were emitting underwater noise exceeding 120 dB.
In the initial testing (I&R 2013a), the noise from the pump and the
associated falling (from deck level) water discharge was found to
exceed 120 dB re 1 [mu]Pa out a distance just beyond 984 ft (300 m).
After the falling water was piped as a mitigation measure to reduce
noise levels, the pump noise was retested (I&R 2013b) with the results
indicating that the primary deep-well pump, operating inside the bow
leg, still exceeded 120 dB re 1 [mu]Pa at a maximum of 853 ft (260 m).
For calculating potential incidental harassment take, the 853-ft (260-
m) distance to the 120 dB isopleth will be used giving a ZOI of 52.5
acres (0.21 km\2\).
4. VSP Airguns
Illingworth and Rodkin (2013c) measured noise levels during VSP
operations associated with Buccaneer post-drilling operations at the
Cosmopolitan 1 site in lower Cook Inlet during July 2013. The
results indicated that the 720 cubic inch airgun array used during the
operation produced noise levels exceeding 160 dB re 1 [mu]Pa out to a
distance of approximately 8,100 ft (2,470 m). Based on these results,
the associated ZOI would be 7.4 mi\2\ (19.2 km\2\).
Marine Mammal Densities
Density estimates were derived for harbor porpoises and harbor
seals as described next. Because of their low numbers, there are no
available Cook Inlet density estimates for the other marine mammals
that occasionally inhabit Cook Inlet north of Anchor Point.
1. Harbor Porpoise
Hobbs and Waite (2010) calculated a Cook Inlet harbor porpoise
density estimate of 0.013 per km\2\ based on sightings recorded during
a summer 1998 aerial survey targeting beluga whales. They derived the
value by dividing estimated number of harbor porpoise inhabiting Cook
Inlet (249) by the area of the entire inlet (18,948 km\2\).
2. Harbor Seal
Boveng et al. (2003) estimated the harbor seal population that
inhabits Cook Inlet at 5,268 seals based on summer/early fall surveys.
Dividing that value by the area of the inlet (18,948 km\2\) provides a
Cook Inlet-wide density of 0.278 seals per km\2\.
Proposed Take Estimates
As noted previously in this document, the potential number of
harbor porpoises and harbor seals that might be exposed to received
continuous SPLs of >=120 dB re 1 [mu]Pa (rms) and pulsed SPLs of >=160
dB re 1 [mu]Pa (rms) was calculated by multiplying:
The expected species density;
the anticipated area to be ensonified by the 120 dB re 1
[mu]Pa (rms) SPL (rig tow and deep-well pumps) and 160 dB re 1 [mu]Pa
(rms) SPL (VSP airgun operations and impact hammering); and
the estimated total duration of each of the activities
expressed in days (24 hrs).
To derive at an estimated total duration for each of the activities
the following assumptions were made:
The total duration for rig tow over the entire season
would be 5 days.
It is estimated to take between 30 and 75 days to drill
one well. Assuming the maximum time needed to drill a well and that up
to two wells may be drilled under this IHA (if issued), the total
duration of deep-well pump usage for two wells would be 150 days.
The total duration of impact hammering during conductor
pipe driving for two wells would be 6 days.
The total duration of the two VSP data acquisition runs is
estimated to be 4 days.
Using all of these assumptions, Table 3 outlines the total number
of Level B harassment exposures for harbor seals and harbor porpoises
from each of the four activities.
Table 3--Potential Number of Exposures to Level B Harassment Thresholds During Buccaneer's Proposed Exploratory
Drilling Program During the 2014 Open Water Season
----------------------------------------------------------------------------------------------------------------
Species Rig tow Deep-well pump Pipe driving VSP Total
----------------------------------------------------------------------------------------------------------------
Harbor porpoise................ 0.05 3 0.9 1 5
Harbor Seal.................... 1.2 9 18.8 21.4 51
----------------------------------------------------------------------------------------------------------------
For the less common marine mammals such as gray, minke, killer
whales, and Dall's porpoise, population estimates within central and
upper Cook Inlet are too small to calculate density estimates. Still,
at even very low densities, it is possible to encounter these marine
mammals during Buccaneer operations, especially during towing
operations through lower Cook Inlet. Marine mammals may approach the
drilling rig out of curiosity, and animals may approach in a group.
Thus, requested take authorizations for these species are primarily
based on group size and the potential for attraction.
Table 4 here outlines the density estimates used to estimate Level
B takes, the proposed Level B harassment take levels, the abundance of
each species in Cook Inlet, the percentage of each species or stock
estimated to be taken, and current population trends.
Table 4--Density Estimates, Proposed Level B Harassment Take Levels, Species or Stock Abundance, Percentage of Population Proposed To Be Taken, and
Species Trend Status
--------------------------------------------------------------------------------------------------------------------------------------------------------
Density
Species ( / Proposed Level Abundance Percentage of Trend
km\2\) B take population
--------------------------------------------------------------------------------------------------------------------------------------------------------
Harbor Seal..................... 0.278 51 22,900............. 0.22 Stable.
Harbor Porpoise................. 0.013 5 25,987............. 0.02 No reliable information.
Killer Whale.................... NA 5 1,123 (resident)... 0.45 Resident stock possibly increasing.
552 (transient) 0.91 Transient stock stable.
[[Page 19276]]
Gray whale...................... NA 2 18,017............. 0.01 Stable/increasing.
Minke whale..................... NA 2 810-1,233.......... 0.16-0.25 No reliable information.
Dall's porpoise................. NA 5 83,400............. 0.01 No reliable information.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Analysis and Preliminary Determinations
Negligible Impact
Negligible impact is ``an impact resulting from the specified
activity that cannot be reasonably expected to, and is not reasonably
likely to, adversely affect the species or stock through effects on
annual rates of recruitment or survival'' (50 CFR 216.103). A
negligible impact finding is based on the lack of likely adverse
effects on annual rates of recruitment or survival (i.e., population-
level effects). An estimate of the number of Level B harassment takes,
alone, is not enough information on which to base an impact
determination. In addition to considering estimates of the number of
marine mammals that might be ``taken'' through behavioral harassment,
NMFS must consider other factors, such as the likely nature of any
responses (their intensity, duration, etc.), the context of any
responses (critical reproductive time or location, feeding, migration,
etc.), as well as the number and nature of estimated Level A harassment
takes, the number of estimated mortalities, effects on habitat, and the
status of the species.
No injuries or mortalities are anticipated to occur as a result of
Buccaneer's proposed exploratory drilling program, and none are
proposed to be authorized. Injury, serious injury, or mortality could
occur if there were a large or very large oil spill. However, as
discussed previously in this document, the likelihood of a spill is
extremely remote. Buccaneer has implemented many design and operational
standards to mitigate the potential for an oil spill of any size. NMFS
does not propose to authorize take from an oil spill, as it is not part
of the specified activity. Additionally, animals in the area are not
expected to incur hearing impairment (i.e., TTS or PTS) or non-auditory
physiological effects. Instead, any impact that could result from
Buccaneer's activities is most likely to be behavioral harassment and
is expected to be of limited duration.
None of the species for which take is proposed to be authorized are
listed as threatened or endangered under the ESA nor as depleted under
the MMPA. Additionally, no critical habitat exists for these species.
Buccaneer's proposed exploratory drilling program will occur south of
critical habitat designated as priority Area 1 for Cook Inlet beluga
whales, but activities will occur in habitat designated as priority
Area 2. During the proposed period of operations, the majority of Cook
Inlet beluga whales will be in Area 1 critical habitat, north of the
proposed drilling area. The proposed activities are not anticipated to
destroy or adversely modify beluga whale critical habitat, and
mitigation measures and safety protocols are in place to reduce any
potential even further.
Sound levels emitted during the proposed program are anticipated to
be low. The continuous sounds produced by the drill rig do not even
rise to the level thought to cause auditory injury in marine mammals.
Additionally, impact hammering and airgun operations will occur for
extremely limited time periods (for a few hours at a time for 1-3 days
per well and for a few hours at a time for 1-2 days per well,
respectively). Moreover, auditory injury has not been noted in marine
mammals from these activities either. Mitigation measures proposed for
inclusion in any issued IHA will reduce these potentials even further.
Potential impacts to marine mammal habitat were discussed
previously in this document (see the ``Anticipated Effects on Habitat''
section). Although some disturbance is possible to food sources of
marine mammals, the impacts are anticipated to be minor enough as to
not affect annual rates of recruitment or survival of marine mammals in
the area. Based on the size of Cook Inlet where feeding by marine
mammals occurs versus the localized area of drilling program
activities, any missed feeding opportunities in the direct project area
would be minor based on the fact that other feeding areas exist
elsewhere. Additionally, drilling operations will not occur in the
primary beluga feeding and calving habitat.
Taking into account the mitigation measures that are planned,
effects on marine mammals are generally expected to be restricted to
avoidance of a limited area around the drilling operation and short-
term changes in behavior, falling within the MMPA definition of ``Level
B harassment''. Animals are not expected to permanently abandon any
area that is part of the drilling operations, and any behaviors that
are interrupted during the activity are expected to resume once the
activity ceases. Only a small portion of marine mammal habitat will be
affected at any time, and other areas within Cook Inlet will be
available for necessary biological functions. Based on the analysis
contained herein of the likely effects of the specified activity on
marine mammals and their habitat, and taking into consideration the
implementation of the proposed monitoring and mitigation measures, NMFS
preliminarily finds that the total marine mammal take from Buccaneer's
proposed exploratory drilling program will have a negligible impact on
the affected marine mammal species or stocks.
Small Numbers
The requested takes proposed to be authorized represent 0.45
percent of the Alaska resident stock and 0.91 percent of the Gulf of
Alaska, Aleutian Island and Bering Sea stock of killer whales (1,123
residents and 552 transients), 0.02 percent of the Gulf of Alaska stock
of approximately 25,987 harbor porpoises, 0.01 percent of the Alaska
stock of approximately 83,400 Dall's porpoises, 0.16-0.25 percent of
the Alaska stock of approximately 810-1,233 minke whales, and 0.01
percent of the eastern North Pacific stock of approximately 18,017 gray
whales. The take request presented for harbor seals represent 0.22
percent of the Cook Inlet/Shelikof stock of approximately 29,175
animals. These take estimates represent the percentage of each species
or stock that could be taken by Level B behavioral harassment if each
animal is taken only once. The numbers of marine mammals taken are
small relative to the affected species or stock sizes. In addition, the
mitigation and monitoring measures (described previously in this
document) proposed for inclusion in the IHA (if issued) are expected to
reduce even further any potential disturbance
[[Page 19277]]
to marine mammals. NMFS preliminarily finds that small numbers of
marine mammals will be taken relative to the populations of the
affected species or stocks.
Impact on Availability of Affected Species for Taking for Subsistence
Uses
Relevant Subsistence Uses
The subsistence harvest of marine mammals transcends the
nutritional and economic values attributed to the animal and is an
integral part of the cultural identity of the region's Alaska Native
communities. Inedible parts of the whale provide Native artisans with
materials for cultural handicrafts, and the hunting itself perpetuates
Native traditions by transmitting traditional skills and knowledge to
younger generations (NOAA, 2007).
The Cook Inlet beluga whale has traditionally been hunted by Alaska
Natives for subsistence purposes. For several decades prior to the
1980s, the Native Village of Tyonek residents were the primary
subsistence hunters of Cook Inlet beluga whales. During the 1980s and
1990s, Alaska Natives from villages in the western, northwestern, and
North Slope regions of Alaska either moved to or visited the south
central region and participated in the yearly subsistence harvest
(Stanek, 1994). From 1994 to 1998, NMFS estimated 65 whales per year
(range 21-123) were taken in this harvest, including those successfully
taken for food and those struck and lost. NMFS has concluded that this
number is high enough to account for the estimated 14 percent annual
decline in the population during this time (Hobbs et al., 2008). Actual
mortality may have been higher, given the difficulty of estimating the
number of whales struck and lost during the hunts. In 1999, a
moratorium was enacted (Public Law 106-31) prohibiting the subsistence
take of Cook Inlet beluga whales except through a cooperative agreement
between NMFS and the affected Alaska Native organizations. Since the
Cook Inlet beluga whale harvest was regulated in 1999 requiring
cooperative agreements, five beluga whales have been struck and
harvested. Those beluga whales were harvested in 2001 (one animal),
2002 (one animal), 2003 (one animal), and 2005 (two animals). The
Native Village of Tyonek agreed not to hunt or request a hunt in 2007,
when no co-management agreement was to be signed (NMFS, 2008a).
On October 15, 2008, NMFS published a final rule that established
long-term harvest limits on the Cook Inlet beluga whales that may be
taken by Alaska Natives for subsistence purposes (73 FR 60976). That
rule prohibits harvest for a 5-year period (2008-2012), if the average
abundance for the Cook Inlet beluga whales from the prior five years
(2003-2007) is below 350 whales. The next 5-year period that could
allow for a harvest (2013-2017), would require the previous five-year
average (2008-2012) to be above 350 whales. The 2008 Cook Inlet Beluga
Whale Subsistence Harvest Final Supplemental Environmental Impact
Statement (NMFS, 2008a) authorizes how many beluga whales can be taken
during a 5-year interval based on the 5-year population estimates and
10-year measure of the population growth rate. Based on the 2008-2012
5-year abundance estimates, no hunt occurred between 2008 and 2012
(NMFS, 2008a). The Cook Inlet Marine Mammal Council, which managed the
Alaska Native Subsistence fishery with NMFS, was disbanded by a
unanimous vote of the Tribes' representatives on June 20, 2012. At this
time, no harvest is expected in 2013 or 2014. Residents of the Native
Village of Tyonek are the primary subsistence users in Knik Arm area.
Data on the harvest of other marine mammals in Cook Inlet are
lacking. Some data are available on the subsistence harvest of harbor
seals, harbor porpoises, and killer whales in Alaska in the marine
mammal stock assessments. However, these numbers are for the Gulf of
Alaska including Cook Inlet, and they are not indicative of the harvest
in Cook Inlet.
Some detailed information on the subsistence harvest of harbor
seals is available from past studies conducted by the Alaska Department
of Fish & Game (Wolfe et al., 2009). In 2008, only 33 harbor seals were
taken for harvest in the Upper Kenai-Cook Inlet area. In the same
study, reports from hunters stated that harbor seal populations in the
area were increasing (28.6%) or remaining stable (71.4%). The specific
hunting regions identified were Anchorage, Homer, Kenai, and Tyonek,
and hunting generally peaks in March, September, and November (Wolfe et
al., 2009).
Potential Impacts to Subsistence Uses
Section 101(a)(5)(D) also requires NMFS to determine that the
authorization will not have an unmitigable adverse effect on the
availability of marine mammal species or stocks for subsistence use.
NMFS has defined ``unmitigable adverse impact'' in 50 CFR 216.103 as:
An impact resulting from the specified activity: (1) That is likely to
reduce the availability of the species to a level insufficient for a
harvest to meet subsistence needs by: (i) Causing the marine mammals to
abandon or avoid hunting areas; (ii) Directly displacing subsistence
users; or (iii) Placing physical barriers between the marine mammals
and the subsistence hunters; and (2) That cannot be sufficiently
mitigated by other measures to increase the availability of marine
mammals to allow subsistence needs to be met.
The primary concern is the disturbance of marine mammals through
the introduction of anthropogenic sound into the marine environment
during the proposed exploratory drilling operation. Marine mammals
could be behaviorally harassed and either become more difficult to hunt
or temporarily abandon traditional hunting grounds. If a large or very
large oil spill occurred, it could impact subsistence species. However,
as previously mentioned one is not anticipated to occur, and measures
have been taken to prevent a large or very large oil spill. The
proposed exploratory drilling program should not have any impacts to
beluga harvests as none currently occur in Cook Inlet, and no takes of
belugas are anticipated or proposed to be authorized. Additionally,
subsistence harvests of other marine mammal species are limited in Cook
Inlet.
Plan of Cooperation or Measures To Minimize Impacts to Subsistence
Hunts
Regulations at 50 CFR 216.104(a)(12) require IHA applicants for
activities that take place in Arctic waters to provide a Plan of
Cooperation or information that identifies what measures have been
taken and/or will be taken to minimize adverse effects on the
availability of marine mammals for subsistence purposes. NMFS
regulations define Arctic waters as waters above 60[deg] N. latitude.
The proposed mitigation measures described earlier in this document
will reduce impacts to any hunts of harbor seals or other marine mammal
species that may occur in Cook Inlet. These measures will ensure that
marine mammals are available to subsistence hunters.
Unmitigable Adverse Impact Analysis and Preliminary Determination
The project will not have any effect on current beluga whale
harvests because no beluga harvest will take place in 2014. Moreover,
no take of belugas is anticipated or proposed to be authorized.
Additionally, the proposed drilling area is not an important native
subsistence site for other subsistence species of marine mammals. Also,
because of the relatively small proportion of marine mammals utilizing
Cook Inlet, the number harvested is
[[Page 19278]]
expected to be extremely low. Therefore, because the proposed program
would result in only temporary disturbances, the drilling program would
not impact the availability of these other marine mammal species for
subsistence uses.
The timing and location of subsistence harvest of Cook Inlet harbor
seals may coincide with Buccaneer's project, but because this
subsistence hunt is conducted opportunistically and at such a low level
(NMFS, 2013c), Buccaneer's program is not expected to have an impact on
the subsistence use of harbor seals. Moreover, hunts are unlikely to
occur in mid-channel waters of Cook Inlet where drilling associated
activities would occur.
NMFS anticipates that any effects from Buccaneer's proposed
exploratory drilling program on marine mammals, especially harbor seals
and Cook Inlet beluga whales, which are or have been taken for
subsistence uses, would be short-term, site specific, and limited to
inconsequential changes in behavior. NMFS does not anticipate that the
authorized taking of affected species or stocks will reduce the
availability of the species to a level insufficient for a harvest to
meet subsistence needs by: (1) Causing the marine mammals to abandon or
avoid hunting areas; (2) directly displacing subsistence users; or (3)
placing physical barriers between the marine mammals and the
subsistence hunters; and that cannot be sufficiently mitigated by other
measures to increase the availability of marine mammals to allow
subsistence needs to be met. In the unlikely event of a major oil spill
in Cook Inlet, there could be major impacts on the availability of
marine mammals for subsistence uses. As discussed earlier in this
document, the probability of a major oil spill occurring over the life
of the project is low. Additionally, Buccaneer developed an ODPCP,
which was reviewed by NMFS and approved by ADEC on August 29, 2012.
Based on the description of the specified activity, the measures
described to minimize adverse effects on the availability of marine
mammals for subsistence purposes, and the proposed mitigation and
monitoring measures, NMFS has preliminarily determined that there will
not be an unmitgable adverse impact on marine mammal availability for
subsistence uses from take incidental to Buccaneer's proposed
activities.
Endangered Species Act (ESA)
Cook Inlet beluga whales are listed as endangered under the ESA.
The U.S. Army Corps of Engineers consulted with NMFS on this proposed
project pursuant to Section 7 of the ESA. On March 23, 2012, NMFS
concluded that the proposed exploratory drilling program in upper Cook
Inlet is not likely to adversely affect beluga whales or their critical
habitat. On May 9, 2013, NMFS received a letter requesting reinitiation
of consultation for Buccaneer's proposed operations due to
modifications to the project plan of operations. On July 8, 2013, NMFS
again concluded that Buccaneer's proposed exploratory drilling program
in upper Cook Inlet is not likely to adversely affect beluga whales or
their designated critical habitat. Mitigation measures laid out in the
Section 7 Letters of Concurrence to ensure no take of beluga whales
have been proposed for inclusion in any issued IHA. Therefore, NMFS'
Office of Protected Resources does not intend to initiate formal
consultation under Section 7 of the ESA.
National Environmental Policy Act (NEPA)
NMFS is currently conducting an analysis, pursuant to NEPA, to
determine whether this proposed IHA may have a significant effect on
the human environment. This analysis will be completed prior to the
issuance or denial of this proposed IHA.
Proposed Authorization
As a result of these preliminary determinations, NMFS proposes to
issue an IHA to Buccaneer for conducting an exploratory drilling
program in upper Cook Inlet during the 2014 open water season, provided
the previously mentioned mitigation, monitoring, and reporting
requirements are incorporated. The proposed IHA language is provided
next.
This section contains a draft of the IHA itself. The wording
contained in this section is proposed for inclusion in the IHA (if
issued).
1. This IHA is valid from date of issuance through October 31,
2014.
2. This IHA is valid only for activities associated with
Buccaneer's upper Cook Inlet exploratory drilling program. The specific
areas where Buccaneer's exploratory drilling operations will occur are
described in the August 2013 IHA application and depicted in Figure 1
of the application.
3. Species Authorized and Level of Take
a. The incidental taking of marine mammals, by Level B harassment
only, is limited to the following species in the waters of Cook Inlet:
i. Odontocetes: 5 harbor porpoise; 5 Dall's porpoise; and 5 killer
whales.
ii. Mysticetes: 2 gray whales and 2 minke whales.
iii. Pinnipeds: 51 harbor seals.
iv. If any marine mammal species not listed in conditions 3(a)(i)
through (iii) are encountered during exploratory drilling operations
and are likely to be exposed to sound pressure levels (SPLs) greater
than or equal to 160 dB re 1 [mu] Pa (rms) for impulse sources or
greater than or equal to 120 dB re 1 [mu] Pa (rms), then the Holder of
this IHA must shut-down the sound source to avoid take.
b. The taking by injury (Level A harassment) serious injury, or
death of any of the species listed in condition 3(a) or the taking of
any kind of any other species of marine mammal is prohibited and may
result in the modification, suspension or revocation of this IHA.
4. The authorization for taking by harassment is limited to the
following acoustic sources (or sources with comparable frequency and
intensity) and from the following activities:
a. airgun array with a total discharge volume of 720 in\3\;
b. continuous drill rig sounds during active drilling operations
and from rig tow; and
c. impact hammer during conductor pipe driving.
5. The taking of any marine mammal in a manner prohibited under
this Authorization must be reported immediately to the Chief, Permits
and Conservation Division, Office of Protected Resources, NMFS or her
designee.
6. The holder of this IHA must notify the Chief of the Permits and
Conservation Division, Office of Protected Resources, at least 48 hours
prior to the start of exploration drilling activities (unless
constrained by the date of issuance of this Authorization in which case
notification shall be made as soon as possible).
7. Mitigation and Monitoring Requirements: The Holder of this
Authorization is required to implement the following mitigation and
monitoring requirements when conducting the specified activities to
achieve the least practicable impact on affected marine mammal species
or stocks:
a. Utilize a sufficient number of NMFS-qualified, vessel-based
Protected Species Observers (PSOs) to visually watch for and monitor
marine mammals near the drill rig during daytime operations (from
nautical twilight-dawn to nautical twilight-dusk) and before and during
start-ups of sound sources day or night. PSOs shall have access to
reticle binoculars, big-eye binoculars, and night vision devices. PSO
shifts shall last no longer than 4 hours at a time. PSOs shall also
make observations during daytime periods when the sound
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sources are not operating for comparison of animal abundance and
behavior, when feasible. When practicable, as an additional means of
visual observation, drill rig or vessel crew may also assist in
detecting marine mammals.
b. When a mammal sighting is made, the following information about
the sighting will be recorded:
i. Species, group size, age/size/sex categories (if determinable),
behavior when first sighted and after initial sighting, heading (if
consistent), bearing and distance from the PSO, apparent reaction to
activities (e.g., none, avoidance, approach, paralleling, etc.),
closest point of approach, and behavioral pace;
ii. Time, location, speed, activity of the vessel, sea state, ice
cover, visibility, and sun glare;
iii. The positions of other vessel(s) in the vicinity of the PSO
location (if applicable);
iv. The rig's position, speed if under tow, and water depth, sea
state, ice cover, visibility, and sun glare will also be recorded at
the start and end of each observation watch, every 30 minutes during a
watch, and whenever there is a change in any of those variables.
c. Within safe limits, the PSOs should be stationed where they have
the best possible viewing;
d. PSOs should be instructed to identify animals as unknown where
appropriate rather than strive to identify a species if there is
significant uncertainty;
e. Conductor Pipe Driving Mitigation Measures:
i. PSOs will observe from the drill rig during impact hammering out
to the 160 dB (rms) radius of 2 km (1.24 mi). If marine mammal species
for which take is not authorized enter this zone, then use of the
impact hammer will cease.
ii. If cetaceans for which take is authorized enter within the 180
dB (rms) radius of 250 m (820 ft) or if pinnipeds for which take is
authorized enter within the 190 dB (rms) radius of 60 m (200 ft), then
use of the impact hammer will cease. Following a shutdown of impact
hammering activities, the applicable zones must be clear of marine
mammals for at least 30 minutes prior to restarting activities.
iii. PSOs will visually monitor out to the 160 dB radius for at
least 30 minutes prior to the initiation of activities. If no marine
mammals are detected during that time, then Buccaneer can initiate
impact hammering using a ``soft start'' technique. Hammering will begin
with an initial set of three strikes at 40 percent energy followed by a
1 min waiting period, then two subsequent three-strike sets. This
``soft-start'' procedure will be implemented anytime impact hammering
has ceased for 30 minutes or more. Impact hammer ``soft-start'' will
not be required if the hammering downtime is for less than 30 minutes
and visuals surveys are continued throughout the silent period and no
marine mammals are observed in the applicable zones during that time.
f. VSP Airgun Mitigation Measures:
i. PSOs will observe from the drill rig during airgun operations
out to the 160 dB radius of 2.5 km (1.55 mi). If marine mammal species
for which take is not authorized enter this zone, then use of the
airguns will cease.
ii. If cetaceans for which take is authorized enter within the 180
dB (rms) radius of 240 m (787 ft) or if pinnipeds for which take is
authorized enter within the 190 dB (rms) radius of 75 m (246 ft), then
use of the airguns will cease. Following a shutdown of airgun
operations, the applicable zones must be clear of marine mammals for at
least 30 minutes prior to restarting activities.
iii. PSOs will visually monitor out to the 160 dB radius for at
least 30 minutes prior to the initiation of activities. If no marine
mammals are detected during that time, then Buccaneer can initiate
airgun operations using a ``ramp-up'' technique. Airgun operations will
begin with the firing of a single airgun, which will be the smallest
gun in the array in terms of energy output (dB) and volume (in\3\).
Operators will then continue ramp-up by gradually activating additional
airguns over a period of at least 30 minutes (but not longer than 40
minutes) until the desired operating level of the airgun array is
obtained. This ramp-up procedure will be implemented anytime airguns
have not been fired for 30 minutes or more. Airgun ramp-up will not be
required if the airguns have been off for less than 30 minutes and
visuals surveys are continued throughout the silent period and no
marine mammals are observed in the applicable zones during that time.
g. No initiation of survey operations involving the use of sound
sources is permitted from a shutdown position at night or during low-
light hours (such as in dense fog or heavy rain).
h. Field Source Verification: The Holder of this IHA is required to
conduct sound source verification tests for the drill rig, impact
hammer, and the airgun array. Sound source verification shall consist
of distances where broadside and endfire directions at which broadband
received levels reach 190, 180, 170, 160, and 120 dB re 1 [mu] Pa (rms)
for all active acoustic sources that may be used during the activities.
Initial results must be provided to NMFS within 1 week of completing
the analysis.
i. Helicopters must maintain an altitude of at least 1,000 ft (305
m), except during takeoffs, landings, or emergency situations.
8. Reporting Requirements: The Holder of this IHA is required to:
a. Submit an SSV report that describes the source of the sound, the
environment, the measurements, and the methodology employed to make the
measurements. Results will be presented as overall sound pressure
levels and displays of 1/3rd octave band sound levels. Preliminary
findings relative to the 120 dB, 160 dB, 180 dB, and 190 dB isopleths
will be provided within 1 week of SSV completion.
b. Submit a draft Technical Report on all activities and monitoring
results to NMFS' Permits and Conservation Division within 90 days of
expiration of the IHA. The Technical Report will include:
i. Summaries of monitoring effort (e.g., total hours, total
distances, and marine mammal distribution through the study period,
accounting for sea state and other factors affecting visibility and
detectability of marine mammals);
ii. Analyses of the effects of various factors influencing
detectability of marine mammals (e.g., sea state, number of observers,
and fog/glare);
iii. Species composition, occurrence, and distribution of marine
mammal sightings, including date, water depth, numbers, age/size/gender
categories (if determinable), group sizes, and ice cover;
iv. Analyses of the effects of drilling operation activities;
v. Sighting rates of marine mammals during periods with and without
drilling operation activities (and other variables that could affect
detectability), such as: (A) Initial sighting distances versus activity
state; (B) closest point of approach versus activity state; (C)
observed behaviors and types of movements versus activity state; (D)
numbers of sightings/individuals seen versus activity state; (E)
distribution around the drill rig versus activity state; and (F)
estimates of take by Level B harassment based on presence in the 120 dB
and 160 dB harassment zones.
c. Submit a final report to the Chief, Permits and Conservation
Division, Office of Protected Resources, NMFS, within 30 days after
receiving comments from NMFS on the draft technical report. If NMFS has
no comments on the draft technical report, the draft report shall be
considered to be the final report.
[[Page 19280]]
9. a. In the unanticipated event that the specified activity
clearly causes the take of a marine mammal in a manner prohibited by
this IHA, such as an injury (Level A harassment), serious injury or
mortality (e.g., ship-strike, gear interaction, and/or entanglement),
Buccaneer shall immediately cease the specified activities and
immediately report the incident to the Chief of the Permits and
Conservation Division, Office of Protected Resources, NMFS, her
designees, and the Alaska Regional Stranding Coordinators. The report
must include the following information:
i. Time, date, and location (latitude/longitude) of the incident;
ii. The name and type of vessel involved;
iii. The vessel's speed during and leading up to the incident;
iv. Description of the incident;
v. Status of all sound source use in the 24 hours preceding the
incident;
vi. Water depth;
vii. Environmental conditions (e.g., wind speed and direction,
Beaufort sea state, cloud cover, and visibility);
viii. Description of marine mammal observations in the 24 hours
preceding the incident;
ix. Species identification or description of the animal(s)
involved;
x. The fate of the animal(s); and
xi. Photographs or video footage of the animal (if equipment is
available).
Activities shall not resume until NMFS is able to review the
circumstances of the prohibited take. NMFS shall work with Buccaneer to
determine what is necessary to minimize the likelihood of further
prohibited take and ensure MMPA compliance. Buccaneer may not resume
their activities until notified by NMFS via letter or email, or
telephone.
b. In the event that Buccaneer discovers an injured or dead marine
mammal, and the lead PSO determines that the cause of the injury or
death is unknown and the death is relatively recent (i.e., in less than
a moderate state of decomposition as described in the next paragraph),
Buccaneer will immediately report the incident to the Chief of the
Permits and Conservation Division, Office of Protected Resources, NMFS,
her designees, and the NMFS Alaska Stranding Hotline. The report must
include the same information identified in the Condition 9(a) above.
Activities may continue while NMFS reviews the circumstances of the
incident. NMFS will work with Apache to determine whether modifications
in the activities are appropriate.
c. In the event that Buccaneer discovers an injured or dead marine
mammal, and the lead PSO determines that the injury or death is not
associated with or related to the activities authorized in Condition 2
of this Authorization (e.g., previously wounded animal, carcass with
moderate to advanced decomposition, or scavenger damage), Buccaneer
shall report the incident to the Chief of the Permits and Conservation
Division, Office of Protected Resources, NMFS, her designees, the NMFS
Alaska Stranding Hotline (1-877-925-7773), and the Alaska Regional
Stranding Coordinators within 24 hours of the discovery. Buccaneer
shall provide photographs or video footage (if available) or other
documentation of the stranded animal sighting to NMFS and the Marine
Mammal Stranding Network. Activities may continue while NMFS reviews
the circumstances of the incident.
10. Activities related to the monitoring described in this IHA do
not require a separate scientific research permit issued under section
104 of the MMPA.
11. A copy of this Authorization must be in the possession of all
contractors and PSOs operating under the authority of this IHA.
12. Penalties and Permit Sanctions: Any person who violates any
provision of this IHA is subject to civil and criminal penalties,
permit sanctions, and forfeiture as authorized under the MMPA.
13. This IHA may be modified, suspended or withdrawn if the Holder
fails to abide by the conditions prescribed herein or if the authorized
taking is having more than a negligible impact on the species or stock
of affected marine mammals, or if there is an unmitigable adverse
impact on the availability of such species or stocks for subsistence
uses.
Request for Public Comments
NMFS requests comment on our analysis, the draft authorization, and
any other aspect of the Notice of Proposed IHA for Buccaneer's proposed
upper Cook Inlet exploratory drilling program. Please include with your
comments any supporting data or literature citations to help inform our
final decision on Buccaneer's request for an MMPA authorization.
Dated: March 31, 2014.
Perry F. Gayaldo,
Acting Deputy Director, Office of Protected Resources, National Marine
Fisheries Service.
[FR Doc. 2014-07601 Filed 4-4-14; 8:45 am]
BILLING CODE 3510-22-P