Takes of Marine Mammals Incidental to Specified Activities; Taking Marine Mammals Incidental to Office of Naval Research Arctic Research Activities, 37240-37262 [2019-16318]
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Federal Register / Vol. 84, No. 147 / Wednesday, July 31, 2019 / Notices
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Dated: July 26, 2019.
Tracey L. Thompson,
Acting Deputy Director, Office of Sustainable
Fisheries, National Marine Fisheries Service.
[FR Doc. 2019–16252 Filed 7–30–19; 8:45 am]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
RIN 0648–XR023
Takes of Marine Mammals Incidental to
Specified Activities; Taking Marine
Mammals Incidental to Office of Naval
Research Arctic Research Activities
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
AGENCY:
Notice; proposed incidental
harassment authorization; request for
comments on proposed authorization
and possible renewal.
ACTION:
NMFS has received a request
from the U.S. Navy’s Office of Naval
Research (ONR) for authorization to take
marine mammals incidental to Arctic
Research Activities in the Beaufort and
Chukchi Seas. Pursuant to the Marine
Mammal Protection Act (MMPA), NMFS
is requesting comments on its proposal
to issue an incidental harassment
authorization (IHA) to incidentally take
marine mammals during the specified
activities. NMFS is also requesting
comments on a possible one-year
renewal that could be issued under
certain circumstances and if all
requirements are met, as described in
Request for Public Comments at the end
of this notice. NMFS will consider
public comments prior to making any
final decision on the issuance of the
requested MMPA authorizations and
agency responses will be summarized in
the final notice of our decision. ONR’s
activities are considered military
readiness activities pursuant to the
Marine Mammal Protection Act
(MMPA), as amended by the National
Defense Authorization Act for Fiscal
Year 2004 (NDAA).
SUMMARY:
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Comments and information must
be received no later than August 30,
2019.
DATES:
Comments should be
addressed to Jolie Harrison, Chief,
Permits and Conservation Division,
Office of Protected Resources, National
Marine Fisheries Service. Physical
comments should be sent to 1315 EastWest Highway, Silver Spring, MD 20910
and electronic comments should be sent
to ITP.Fowler@noaa.gov.
Instructions: NMFS is not responsible
for comments sent by any other method,
to any other address or individual, or
received after the end of the comment
period. Comments received
electronically, including all
attachments, must not exceed a 25megabyte file size. Attachments to
electronic comments will be accepted in
Microsoft Word or Excel or Adobe PDF
file formats only. All comments
received are a part of the public record
and will generally be posted online at
https://www.fisheries.noaa.gov/permit/
incidental-take-authorizations-undermarine-mammal-protection-act 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.
FOR FURTHER INFORMATION CONTACT:
Amy Fowler, Office of Protected
Resources, NMFS, (301) 427–8401.
Electronic copies of the application and
supporting documents, as well as a list
of the references cited in this document,
may be obtained online at: https://
www.fisheries.noaa.gov/permit/
incidental-take-authorizations-undermarine-mammal-protection-act. In case
of problems accessing these documents,
please call the contact listed above.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
Background
The MMPA prohibits the ‘‘take’’ of
marine mammals, with certain
exceptions. Sections 101(a)(5)(A) and
(D) of the MMPA (16 U.S.C. 1361 et
seq.) direct the Secretary of Commerce
(as delegated to NMFS) 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
incidental take authorization may be
provided to the public for review.
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Authorization for incidental takings
shall be granted if NMFS finds that the
taking will have a negligible impact on
the species or stock(s) and will not have
an unmitigable adverse impact on the
availability of the species or stock(s) for
taking for subsistence uses (where
relevant). Further, NMFS must prescribe
the permissible methods of taking and
other ‘‘means of effecting the least
practicable adverse impact’’ on the
affected species or stocks and their
habitat, paying particular attention to
rookeries, mating grounds, and areas of
similar significance, and on the
availability of such species or stocks for
taking for certain subsistence uses
(referred to in shorthand as
‘‘mitigation’’); and requirements
pertaining to the mitigation, monitoring
and reporting of such takings are set
forth.
The NDAA (Pub. L. 108–136)
removed the ‘‘small numbers’’ and
‘‘specified geographical region’’
limitations indicated above and
amended the definition of ‘‘harassment’’
as it applies to a ‘‘military readiness
activity.’’ The activity for which
incidental take of marine mammals is
being requested addressed here qualifies
as a military readiness activity. The
definitions of all applicable MMPA
statutory terms cited above are included
in the relevant sections below. The
proposed action constitutes a military
readiness activity because these
proposed scientific research activities
directly support the adequate and
realistic testing of military equipment,
vehicles, weapons, and sensors for
proper operation and suitability for
combat use by providing critical data on
the changing natural and physical
environment in which such materiel
will be assessed and deployed. This
proposed scientific research also
directly supports fleet training and
operations by providing up to date
information and data on the natural and
physical environment essential to
training and operations.
Accordingly, NMFS plans to adopt
the Navy’s Environmental Assessment/
Overseas Environmental Assessment,
provided our independent evaluation of
the document finds that it includes
adequate information analyzing the
effects on the human environment of
issuing the IHA. The Navy’s OEA is
available at https://
www.fisheries.noaa.gov/permit/
incidental-take-authorizations-undermarine-mammal-protection-act.
We will review all comments
submitted in response to this notice
prior to concluding our NEPA process
or making a final decision on the IHA
request.
National Environmental Policy Act
Overview
ONR’s Arctic Research Activities
include scientific experiments to be
conducted in support of the programs
named above. Specifically, the project
includes the Stratified Ocean Dynamics
of the Arctic (SODA), Arctic Mobile
Observing System (AMOS), Ocean
Acoustics field work (including the
Coordinated Arctic Active Tomography
To comply with the National
Environmental Policy Act of 1969
(NEPA; 42 U.S.C. 4321 et seq.) and
NOAA Administrative Order (NAO)
216–6A, NMFS must review our
proposed action (i.e., the issuance of an
incidental harassment authorization)
with respect to potential impacts on the
human environment.
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Summary of Request
On April 25, 2019, NMFS received a
request from ONR for an IHA to take
marine mammals incidental to Arctic
Research Activities in the Beaufort and
Chukchi Seas. The application was
deemed adequate and complete on July
16, 2019. ONR’s request is for take of a
small number of beluga whales
(Delphinapterus leucas), bearded seals
(Erignathus barbatus), and ringed seals
(Pusa hispida hispida) by Level B
harassment only. Neither ONR nor
NMFS expects serious injury or
mortality to result from this activity
and, therefore, an IHA is appropriate.
This proposed IHA would cover the
second year of a larger project for which
ONR obtained a prior IHA and intends
to request take authorization for
subsequent facets of the project. This
IHA would be valid for a period of one
year from the date of issuance. The
larger three-year project involves several
scientific objectives which support the
Arctic and Global Prediction Program,
as well as the Ocean Acoustics Program
and the Naval Research Laboratory, for
which ONR is the parent command.
ONR complied with all the
requirements (e.g., mitigation,
monitoring, and reporting) of the
previous IHA (83 FR 48799; September
27, 2019).
Description of Proposed Activity
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Experiment (CAATEX)), and Naval
Research Laboratory experiments in the
Beaufort and Chukchi Seas. These
experiments involve deployment of
moored and ice-tethered active acoustic
sources, primarily from the U.S Coast
Guard Cutter (CGC) HEALY. CGC
HEALY may also be required to perform
icebreaking to deploy the acoustic
sources in deep water. Underwater
sound from the acoustic sources and
icebreaking may result in behavioral
harassment of marine mammals.
Dates and Duration
ONR’s Arctic Research Activities
began in August 2018 with deployment
of autonomous gliders in the Beaufort
and Chukchi Seas and subsequent
deployment of moored acoustic sources
in September 2018. The activities
analyzed in this proposed IHA would
begin in September 2019, with a
tentative sail date of September 3, 2019.
CGC HEALY would perform a research
cruise for up to 60 days in September
and October 2019 to deploy acoustic
sources. If required, a second, nonicebreaking ship would perform a cruise
of up to 30 days to deploy any
remaining sources in the fall of 2019. A
total of eight days of icebreaking within
the effective dates of this IHA are
anticipated to be required to deploy
and/or retrieve the northernmost
acoustic sources. CGC HEALY, a similar
icebreaking ship, or a non-icebreaking
ship would be used for a subsequent
research cruise for up to 60 days
beginning in August 2020. The initial
stages of the August 2020 cruise (i.e., the
spiral wave beacon, see Detailed
Description of Specific Activity below)
are included in the activities analyzed
in this IHA. The latter stages of the 2020
cruise would be analyzed in a
subsequent IHA
Specific Geographic Region
The proposed actions would occur in
either the U.S. Exclusive Economic
Zone (EEZ) or the high seas north of
Alaska (Figure 1). All activities, except
for the transit of ships, would take place
outside U.S. territorial waters. The total
area of the study area is 835,860 square
kilometers (km2) (322,727 square miles
(mi2)). The closest active acoustic
source (aside from de minimis sources
described below) within the study area
is approximately 145 miles (mi; 233
kilometers (km)) from land.
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Arctic Research Activities Study Area 2019
•
Spiral Wave Beacon
CMTEX Receiver
2018 Study Area Boundary
De minimis Mooring
CAATEX Source
De minimis PIES Sources
Alternative CAATEX Source Location
Kilometers
•
Drifting Sources
U.S. Territorial Seas
H
Moored Sources
0 50 100 150 200
ARA Study Area
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tern: WGS 1984, North Pole LAEAA!aska
Figure 1. Arctic Research Activities
Study Area
Detailed Description of Specific Activity
The ONR Arctic and Global
Prediction Program is supporting two
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major projects (SODA and AMOS),
which will both occur during time
period covered by this IHA. The SODA
project began field work in August 2018,
consisting of research cruises and the
deployment of autonomous
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Date: 21 March 2019 Data Source: Esri US Nav . ONR CoordinateS
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measurement devices for year-round
observation of water properties
(temperature and salinity) and the
associated stratification and circulation.
These physical processes are related to
the ice cover and as the properties of the
ice cover change, the water properties
will change as well. Warm water feeding
into the Arctic Ocean also plays an
important role changing the
environment. Observations of these
phenomena require geographical
sampling of areas of varying ice cover
and temperature profile, and year-round
temporal sampling to understand what
happens during different parts of the
year. Unmanned gliders and
autonomous platforms are needed for
this type of year-round observation of a
representative sample of arctic waters.
The SODA project also involved the
initial deployment of navigation sources
for unmanned vehicles. Under the
AMOS project, there will be new
deployments of navigation sources in
September 2019 (Figure 1). Geolocation
of autonomous platforms requires the
use of acoustic navigation signals, and
therefore, year-long use of active
acoustic signals.
The ONR Ocean Acoustics Program
also supports Arctic field work. The
emphasis of the Ocean Acoustics
Program field efforts is to understand
how the changing environment affects
acoustic propagation and the noise
environment. The ONR Acoustic
Program would be utilizing new
technology for year-round observation
of the large-scale (range and depth)
temperature structure of the ocean at
very low frequencies. The use of
specialized waveforms and acoustic
arrays allows signals to be received over
100 km from a source, while only
requiring moderate source levels. The
Ocean Acoustics program is planning to
perform experiments in conjunction
with the Arctic and Global Prediction
Program by operating in the same
general location and with the same
research vessel.
The Naval Research Laboratory would
also conduct Arctic research in the same
time frame, using drifting buoys with
active acoustic sources that are
deployed in the ice. The buoys are
deployed for real-time environmental
characterization to aid in mid-frequency
sonar performance predictions. Realtime assimilation of acoustic data into
an ocean model is also planned.
Below are descriptions of the
equipment and platforms that would be
deployed at different times during the
proposed action.
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Research Vessels
CGC HEALY would be the primary
vessel performing the research cruise in
September and October 2019. CGC
HEALY travels at a maximum speed of
17 knots (kn) with a cruising speed of
12 kn (United States Coast Guard 2013),
and a maximum speed of 3 kn when
traveling through 3.5 feet (ft; 1.07 meters
(m)) of sea ice (Murphy 2010). CGC
HEALY may be required to perform
icebreaking to deploy the moored and
ice tethered acoustic sources in deep
water. Icebreaking would only occur
during the warm season, presumably in
the August through October timeframe.
CGC HEALY has proven capable of
breaking ice up to 8 ft (2.4 m) thick
while backing and ramming (Roth et al.
2013). A study in the western Arctic
Ocean was conducted while CGC
HEALY was mapping the seafloor north
of the Chukchi Cap in August 2008.
During this study, CGC HEALY
icebreaker events generated signals with
frequency bands centered near 10, 50,
and 100 Hertz (Hz) with maximum
source levels of 190 to 200 decibel(s)
(dB) referenced to 1 microPascal (mPa) at
1 meter (dB re 1 mPa at 1 m; full octave
band) (Roth et al. 2013). Icebreaking
would likely only occur in the
northernmost areas of the study area
while deploying and/or retrieving
sources.
The CGC HEALY or other vessels may
perform the following activities during
the research cruises (some of these
activities may result in take of marine
mammals, while others may not, as
described further below):
• Deployment of moored and/or icetethered passive sensors (e.g.,
oceanographic measurement devices,
acoustic receivers);
• Deployment of moored and/or icetethered active acoustic sources to
transmit acoustic signals for up to two
years after deployment. Transmissions
could be terminated during ice-free
periods (August-October) each year, if
needed;
• Deployment of unmanned surface,
underwater, and air vehicles; and
• Recovery of equipment.
Additional oceanographic
measurements would be made using
ship-based systems, including the
following:
• Modular Microstructure Profiler, a
tethered profiler that would measure
oceanographic parameters within the
top 984 ft (300 m) of the water column;
• Shallow Water Integrated Mapping
System, a winched towed body with a
Conductivity Temperature Depth
sensor, upward and downward looking
Acoustic Doppler Current Profilers
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(ADCPs), and a temperature sensor
within the top 328 ft (100 m) of the
water column;
• Three-dimensional Sonic
Anemometer, which would measure
wind stress from the foremast of the
ship;
• Surface Wave Instrument Float with
Tracking (SWIFTs) buoys are freely
drifting buoys measuring winds, waves,
and other parameters with deployments
spanning from hours to days; and
• A single mooring would be
deployed to perform measurements of
currents with an ADCP.
Moored and Drifting Acoustic Sources
Up to 15 moored acoustic navigation
sources would be deployed during the
period September 2019 to September
2020 at the locations shown in Figure 1.
Each navigation source transmits for 8
seconds every 4 hours, with the sources
transmitting with a five minute offset
from each other. The purpose of the
navigation sources is to allow
autonomous vehicles and gliders to
navigate by receiving acoustic signals
from multiple locations and
triangulating position. This is needed
for vehicles that are under ice and
cannot communicate with satellites.
A single very low frequency (VLF)
source would be deployed in the
furthest north part of the study area,
shown by the triangle symbols in Figure
1. The northernmost location is the
preferred location, but the alternative
location may be used. The VLF source
provides capability for persistent (yearlong) observation of Arctic
oceanographic processes and measures
oceanographic changes (e.g. regional
increases in temperature) over long
ranges.
All moorings would be anchored on
the seabed and held in the water
column with subsurface buoys. All
sources would be deployed by
shipboard winches, which would lower
sources and receivers in a controlled
manner. Anchors would be steel
‘‘wagon wheels’’ typically used for this
type of deployment.
Up to six drifting sources would be
deployed for the purpose of near-real
time environmental characterization,
which is accomplished by
communicating information from the
drifting buoys to a satellite. They would
be deployed in the ice for purposes of
buoy stability, but would eventually
drift in open water. The sources would
transmit signals to each other to
measure oceanographic properties of the
water between them. The sources would
stop transmitting when this IHA expires
in September 2020 or when they leave
the Study Area, whichever comes first.
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On the fall 2020 cruise, a spiral wave
beacon source would be tested for finescale navigation. The spiral wave
beacon is a mid-frequency source that
transmits a 50 millisecond signal at 30
second intervals. The source would be
deployed from a ship at a single location
and transmit for up to 5 days. It will
either be attached to the ship or moored
near the ship. The ship will remain for
the 5 days of the test, and the source
will be recovered at the end of testing.
TABLE 1—CHARACTERISTICS OF PROPOSED ACOUSTIC SOURCES
Frequency
range (Hz)
Source name
Sound pressure level
(dB re 1 μPa
at 1 m)
Pulse length
(milliseconds)
Duty cycle
(percent)
Source type
Usage
15 sources transmitting 8 seconds every 4
hours, up to 2 years.
6 sources transmitting 1 minute every 4
hours, up to 2 years.
5 days.
One source transmitting 30 minutes every
6 days, up to 2 years.
Navigation Sources ....................................
900
185 ................
8,000
<1
Moored .........
Real-Time Sensing Sources .......................
900 to 1000
184 ................
60,000
<1
Drifting ..........
Spiral Wave Beacon ...................................
Very Low Frequency (VLF source) ............
2,500
34
183 ................
185 (peak) ....
50
1,800,000
<1
<1
Moored .........
Moored .........
Activities Not Likely to Result in Take
The following in-water activities have
been determined to be unlikely to result
in take of marine mammals. These
activities are described here but their
effects are not described further in this
document.
De minimis Sources—De minimis
sources have the following parameters:
Low source levels, narrow beams,
downward directed transmission, short
pulse lengths, frequencies outside
known marine mammal hearing ranges,
or some combination of these factors
(Department of the Navy 2013b). For
further detail regarding the de minimis
sources planned for use by the Navy,
which are not quantitatively analyzed,
please see the Navy’s application.
Descriptions of example sources are
provided below and in Table 2.
TABLE 2—PARAMETERS FOR De Minimis SOURCES
Sound
pressure
level
(dB re 1
μPa at 1 m)
Pulse length
(milli-seconds)
Source name
Frequency
range (kHz)
Pressure Inverted Echosounders (PIES) ...
12 ..................
170–180
6
ADCP ..........................................................
>200, 150, or
75.
2–16 ..............
190
Chirp sonar .................................................
Expendable Mobile Anti-Submarine Warfare Training Targets (EMATTs).
Coring system .............................................
CTD1 attached Echosounder .....................
1 CTD
700–1100 Hz
and 1100–
4000 Hz.
25–200 ..........
5–20 ..............
Duty cycle
(percent)
Beamwidth
De minimis justification
<0.01
45 ..................
<1
<0.1
2.2 .................
200
20
<1
narrow ...........
<150
N/A
25–100
Omni .............
Extremely low duty cycle, low source
level, very short pulse length.
Very low pulse length, narrow beam, moderate source level.
Very short pulse length, low duty cycle,
narrow beam width.
Very low source level.
158–162
160
<1
4
16
2
Omni .............
Omni .............
Very low source level.2
Very low source level.
= Conductivity Temperature Depth.
sediment, not within the water column.
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2 Within
Drifting Oceanographic Sensors—
Observations of ocean-ice interactions
require the use of sensors which are
moored and embedded in the ice.
Sensors are deployed within a few
dozen meters of each other on the same
ice floe. Three types of sensors would be
used: Autonomous Ocean Flux Buoys,
Integrated Autonomous Drifters, and Ice
Tethered Profilers. The autonomous
ocean flux buoys measure
oceanographic properties just below the
ocean-ice interface. The autonomous
ocean flux buoys would have ADCPs
and temperature chains attached, to
measure temperature, salinity, and other
ocean parameters in the top 20 ft (6 m)
of the water column. Integrated
Autonomous Drifters would have a long
temperature string extending down to
656 ft (200 m) depth and would
incorporate meteorological sensors, and
a temperature string to estimate ice
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thickness. The Ice Tethered Profilers
would collect information on ocean
temperature, salinity, and velocity down
to 820 ft (250 m) depth.
Fifteen autonomous floats (AirLaunched Autonomous Micro
Observers) would be deployed during
the proposed action to measure seasonal
evolution of the ocean temperature and
salinity, as well as currents. They would
be deployed on the eastern edge of the
Chukchi Sea in water less than 3,280 ft
(1,000 m) deep. Three autonomous
floats would act as virtual moorings by
originating on the seafloor, then moving
up the water column to the surface and
returning to the seafloor. The other 12
autonomous floats would sit on the sea
floor and at intervals begin to move
toward the surface. At programmed
intervals, a subset of the floats would
release anchors and begin their profiling
mission. Up to 15 additional floats may
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be deployed by ships of opportunity in
the Beaufort Gyre.
The drifting oceanographic sensors
described above use only de minimis
sources and are therefore not
anticipated to have the potential for
impacts on marine mammals or their
habitat.
Moored Oceanographic Sensors—
Moored sensors would capture a range
of ice, ocean, and atmospheric
conditions on a year-round basis. The
location of the bottom-anchored subsurface moorings are depicted by the
purple stars in Figure 1–1 of the IHA
application. These would be bottomanchored, sub-surface moorings
measuring velocity, temperature, and
salinity in the upper 1,640 ft (500 m) of
the water column. The moorings also
collect high-resolution acoustic
measurements of the ice using the ice
profilers described above. Ice velocity
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and surface waves would be measured
by 500 kHz multibeam sonars.
Additionally, Beaufort Gyre
Exploration Project moorings BGOS–A
and BGOS–B (depicted by the black
plus signs in Figure 1–1 of the IHA
application) would be augmented with
McLane Moored Profilers. BGOS–A and
BGOS–B would provide measurements
near the Northwind Ridge, with
considerable latitudinal distribution.
Existing deployments of Nortek
Acoustic Wave and Current Profilers on
BGOS–A and BGOS–B would also be
continued as part of the proposed
action.
The moored oceanographic sensors
described above use only de minimis
sources and are therefore not
anticipated to have the potential for
impacts on marine mammals or their
habitat.
Fixed and Towed Receiving Arrays—
Horizontal and vertical arrays may be
used to receive acoustic signals. Two
receiving arrays will be deployed in
September-October 2020 to receive
signals from the CAATEX source. Other
receiving arrays are the Single
Hydrophone Recording Units and
Autonomous Multichannel Acoustic
Recorder. All these arrays would be
moored to the seafloor and remain in
place throughout the activity.
These are passive acoustic sensors
and therefore are not anticipated to have
the potential for impacts on marine
mammals or their habitat.
Activities Involving Aircraft and
Unmanned Air Vehicles—Naval
Research Laboratory would be
conducting flights to characterize the ice
structure and character, ice edge and
wave heights across the open water and
marginal ice zone to the ice. Up to 4
flights, lasting approximately 3 hours in
duration would be conducted over a 10
day period during February or March for
ice structure and character
measurements and during late summer/
early fall for ice edge and wave height
studies. Flights would be conducted
with a Twin Otter aircraft over the
seafloor mounted acoustic sources and
receivers. Most flights would transit at
1,500 ft or 10,000 ft (457 or 3,048 m)
above sea level. Twin Otters have a
typical survey speed of 90 to 110 kn, 66
ft (20 m) wing span, and a total length
of 26 ft (8 m) (U.S. Department of
Commerce and NOAA 2015). At a
distance of 2,152 ft (656 m) away, the
received pressure levels of a Twin Otter
range from 80 to 98.5 A-weighted dB
(expression of the relative loudness in
the air as perceived by the human ear)
and frequency levels ranging from 20 Hz
to 10 kHz, though they are more
typically in the 500 Hz range (Metzger
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1995). The objective of the flights is to
characterize thickness and physical
properties of the ice mass overlying the
experiment area.
Rotary wing aircraft may also be used
during the activity. Helicopter transit
would be no longer than two hours to
and from the ice location. A twin engine
helicopter may be used to transit
scientists from land to an offshore
floating ice location. Once on the
floating ice, the team would drill holes
with up to a 10 inch (in; 25.4 centimeter
(cm)) diameter to deploy scientific
equipment (e.g., source, hydrophone
array, EMATT) into the water column.
The science team would depart the area
and return to land after three hours of
data collection and leave the equipment
and leave the equipment behind for a
later recovery.
The proposed action includes the use
of an Unmanned Aerial System (UAS).
The UAS would be deployed ahead of
the ship to ensure a clear passage for the
vessel and would have a maximum
flight time of 20 minutes. The UAS
would not be used for marine mammal
observations or hover close to the ice
near marine mammals. The UAS that
would be used during the proposed
action is a small commercially available
system that generates low sound levels
and is smaller than military grade
systems. The dimensions of the
proposed UAS are, 11.4 in (29 cm) by
11.4 in (29 cm) by 7.1 in (18 cm) and
weighs 2.5 lb (1.13 kg). The UAS can
operate up to 984 ft (300 m) away,
which would keep the device in close
proximity to the ship. The planned
operation of the UAS is to fly it
vertically above the ship to examine the
ice conditions in the path of the ship
and around the area (i.e., not flown at
low altitudes around the vessel).
Currently acoustic parameters are not
available for the proposed models of
UASs to be used. As stated previously,
these systems are small and are similar
to a remote control helicopter. It is
likely marine mammals would not hear
the device since the noise generated
would likely not be audible from greater
than 5 ft (1.5 m) away (Christiansen et
al., 2016).
All aircraft (manned and unmanned)
would be required to maintain a
minimum separation distance of 1,000 ft
(305 m) from any pinnipeds hauled out
on the ice. Therefore, no take of marine
mammals is anticipated from these
activities.
On-Ice Measurement Systems—On-ice
measurement systems would be used to
collect weather data. These would
include an Autonomous Weather
Station and an Ice Mass Balance Buoy.
The Autonomous Weather Station
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would be deployed on a tripod; the
tripod has insulated foot platforms that
are frozen into the ice. The system
would consist of an anemometer,
humidity sensor, and pressure sensor.
The Autonomous Weather Station also
includes an altimeter that is de minimis
due to its very high frequency (200
kHz). The Ice Mass Balance Buoy is a 20
ft (6 m) sensor string, which is deployed
through a 2 in (5 cm) hole drilled into
the ice. The string is weighted by a 2.2
lb (1 kg) lead weight, and is supported
by a tripod. The buoy contains a de
minimis 200 kHz altimeter and snow
depth sensor. Autonomous Weather
Stations and Ice Mass Balance Buoys
will be deployed, and will drift with the
ice, making measurements, until their
host ice floes melt, thus destroying the
instruments (likely in summer, roughly
one year after deployment). After the
on-ice instruments are destroyed they
cannot be recovered, and would sink to
the seafloor as their host ice floes
melted.
All personnel conducting experiments
on the ice would be required to
maintain a minimum separation
distance of 1,000 ft (305 m) from any
pinnipeds hauled out on the ice.
Therefore, no take of marine mammals
is anticipated from these activities.
Bottom Interaction Systems—Coring
of bottom sediment could occur
anywhere within the study area to
obtain a more complete understanding
of the Arctic environment. Coring
equipment would take up to 50 samples
of the ocean bottom in the study area
annually. The samples would be
roughly cylindrical, with a 3.1 in (8 cm)
diameter cross-sectional area; the
corings would be between 10 and 20 ft
(3 and 6 m) long. Coring would only
occur during research cruises, during
the summer or early fall. The coring
equipment moves slowly through the
muddy bottom, at a speed of
approximately 1 m per hour, and would
not create any detectable acoustic signal
within the water column, though very
low levels of acoustic transmissions
may be created in the mud (see
parameters listed in Table 2).
Weather Balloons—To support
weather observations, up to 40 Kevlar or
latex balloons would be launched per
year for the duration of the proposed
action. These balloons and associated
radiosondes (a sensor package that is
suspended below the balloon) are
similar to those that have been deployed
by the National Weather Service since
the late 1930s. When released, the
balloon is approximately 5 to 6 ft (1.5–
1.8 m) in diameter and gradually
expands as it rises due to the decrease
in air pressure. When the balloon
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reaches a diameter of 13–22 ft (4–7 m),
it bursts and a parachute is deployed to
slow the descent of the associated
radiosonde. Weather balloons would not
be recovered.
The deployment of weather balloons
does not include the use of active
acoustics and is therefore not
anticipated to have the potential for
impacts on marine mammals or their
habitat.
Proposed mitigation, monitoring, and
reporting measures are described in
detail later in this document (please see
Proposed Mitigation and Proposed
Monitoring and Reporting).
Description of Marine Mammals in the
Area of Specified Activities
Sections 3 and 4 of the application
summarize available information
regarding status and trends, distribution
and habitat preferences, and behavior
and life history, of the potentially
affected species. Additional information
regarding population trends and threats
may be found in NMFS’s Stock
Assessment Reports (SARs; https://
www.fisheries.noaa.gov/national/
marine-mammal-protection/marinemammal-stock-assessments) and more
general information about these species
(e.g., physical and behavioral
descriptions) may be found on NMFS’s
website (https://
www.fisheries.noaa.gov/find-species).
Table 3 lists all species with expected
potential for occurrence in the study
area and summarizes information
related to the population or stock,
including regulatory status under the
MMPA and ESA and potential
biological removal (PBR), where known.
For taxonomy, we follow Committee on
Taxonomy (2018). PBR is defined by the
MMPA as the maximum number of
animals, not including natural
mortalities, that may be removed from a
marine mammal stock while allowing
that stock to reach or maintain its
optimum sustainable population (as
described in NMFS’s SARs). While no
mortality is anticipated or authorized
here, PBR and annual serious injury and
mortality from anthropogenic sources
are included here as gross indicators of
the status of the species and other
threats.
Marine mammal abundance estimates
presented in this document represent
the total number of individuals that
make up a given stock or the total
number estimated within a particular
study or survey area. NMFS’s stock
abundance estimates for most species
represent the total estimate of
individuals within the geographic area,
if known, that comprises that stock. For
some species, this geographic area may
extend beyond U.S. waters. All managed
stocks in this region are assessed in
NMFS’s U.S. 2018 SARs (e.g., Muto et
al., 2019, Carretta et al., 2019). All
values presented in Table 3 are the most
recent available at the time of
publication and are available in the
2018 SARs (Muto et al., 2019; Carretta
et al., 2019).
TABLE 3—MARINE MAMMAL SPECIES POTENTIALLY PRESENT IN THE PROJECT AREA
Common name
Scientific name
ESA/
MMPA
status;
strategic
(Y/N) 1
Stock
Stock abundance (CV, Nmin,
most recent abundance survey) 2
PBR
Annual
M/SI 3
Order Cetartiodactyla—Cetacea—Superfamily Mysticeti (baleen whales)
Family Eschrichtiidae:
Gray whale .......................
Family Balaenidae:
Bowhead whale ................
Eschrichtius robustus .............
Eastern North Pacific .............
-/- ; N
26960 (0.05, 25,849, 2016) ...
801
135
Balaena mysticetus ................
Western Arctic ........................
E/D ; Y
16,820 (0.052, 16,100, 2011)
161
46
39,258 (0.229, N/A, 1992) .....
20,752 (0.70, 12.194, 2012) ..
4 Undet
244
139
67
299,174 ..................................
(-, 273,676, 2013) ..................
184,697 ..................................
(-, 163,086, 2013) ..................
170,000 ..................................
(-, 170,000, 2013) ..................
461,625 ..................................
(-, 423,237, 2013) ..................
8,210
557
9,785
3.9
5,100
1,054
12,697
329
Superfamily Odontoceti (toothed whales, dolphins, and porpoises)
Family Delphinidae:
Beluga whale ...................
Beluga whale ...................
Delphinapterus leucas ............
Delphinapterus leucas ............
Beaufort Sea ..........................
Eastern Chukchi Sea .............
-/- ; N
-/- ; N
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Order Carnivora—Superfamily Pinnipedia
Family Phocidae (earless
seals):
Bearded seal 5 ..................
Erignathus barbatus ...............
Alaska .....................................
T/D ; Y
Ribbon seal ......................
Histriophoca fasciata ..............
Alaska .....................................
-/- ; N
Ringed seal 5 ....................
Pusa hispida hispida ..............
Alaska .....................................
T/D ; Y
Spotted seal .....................
Phoca largha ..........................
Alaska .....................................
-/- ; N
1 Endangered Species Act (ESA) status: Endangered (E), Threatened (T)/MMPA status: Depleted (D). A dash (-) indicates that the species is not listed under the
ESA or designated as depleted under the MMPA. Under the MMPA, a strategic stock is one for which the level of direct human-caused mortality exceeds PBR or
which is determined to be declining and likely to be listed under the ESA within the foreseeable future. Any species or stock listed under the ESA is automatically
designated under the MMPA as depleted and as a strategic stock.
2 NMFS marine mammal stock assessment reports online at: https://www.fisheries.noaa.gov/national/marine-mammal-protection/marine-mammal-stock-assessmentreports-region/. CV is coefficient of variation; Nmin is the minimum estimate of stock abundance. In some cases, CV is not applicable.
3 These values, found in NMFS’s SARs, represent annual levels of human-caused mortality plus serious injury from all sources combined (e.g., commercial fisheries, ship strike). Annual M/SI often cannot be determined precisely and is in some cases presented as a minimum value or range. A CV associated with estimated
mortality due to commercial fisheries is presented in some cases.
4 The 2016 guidelines for preparing SARs state that abundance estimates older than 8 years should not be used to calculate PBR due to a decline in the reliability
of an aged estimate. Therefore, the PBR for this stock is considered undetermined.
5 Abundances and associated values for bearded and ringed seals are for the U.S. population in the Bering Sea only.
Note: Italicized species are not expected to be taken or proposed for authorization.
All species that could potentially
occur in the proposed survey areas are
included in Table 3. Activities
conducted during the proposed action
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are expected to cause harassment, as
defined by the MMPA as it applies to
military readiness, to the beluga whale
(of the Beaufort and Eastern Chukchi
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Sea stocks), bearded seal, and ringed
seal. Due to the location of the study
area (i.e., northern offshore, deep water),
there were no calculated exposures for
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the bowhead whale, gray whale, spotted
seal, and ribbon seal from quantitative
modeling of non-impulsive acoustic and
icebreaking sources. Bowhead and gray
whales remain closely associated with
the shallow waters of the continental
shelf in the Beaufort Sea and are
unlikely to be exposed to acoustic
harassment (Carretta et al., 2017; Muto
et al., 2018). Similarly, spotted seals
tend to prefer pack ice areas with water
depths less than 200 m during the
spring and move to coastal habitats in
the summer and fall, found as far north
as 69–72° N (Muto et al., 2018).
Although the study area includes waters
south of 72° N, the acoustic sources
with the potential to result in take of
marine mammals are not found below
that latitude and spotted seals are not
expected to be exposed. Ribbon seals are
found year-round in the Bering Sea but
may seasonally range into the Chukchi
Sea (Muto et al., 2018). The proposed
action occurs primarily in the Beaufort
Sea, outside of the core range of ribbon
seals, thus ribbon seals are not expected
to be behaviorally harassed. Narwhals
are considered extralimital in the
project area and are not expected to be
encountered or taken. As no harassment
is expected of bowhead whales, gray
whales, spotted seals, and ribbon seals,
these species will not be discussed
further in this IHA.
Beluga Whale
Beluga whales are distributed
throughout seasonally ice-covered arctic
and subarctic waters of the Northern
Hemisphere (Gurevich 1980), and are
closely associated with open leads and
polynyas in ice-covered regions (Hazard
1988). Belugas are both migratory and
residential (non-migratory), depending
on the population. Seasonal distribution
is affected by ice cover, tidal conditions,
access to prey, temperature, and human
interaction (Frost et al., 1985).
There are five beluga stocks
recognized within U.S. waters: Cook
Inlet, Bristol Bay, eastern Bering Sea,
eastern Chukchi Sea, and Beaufort Sea.
Two stocks, the Beaufort Sea and
eastern Chukchi Sea stocks, have the
potential to occur in the Study Area.
There are two migration areas used by
Beaufort Sea belugas that overlap the
Study Area. One, located in the Eastern
Chukchi and Alaskan Beaufort Sea, is a
migration area in use from April to May.
The second, located in the Alaskan
Beaufort Sea, is used by migrating
belugas from September to October
(Calambokidis et al., 2015). During the
winter, they can be found foraging in
offshore waters associated with pack
ice. When the sea ice melts in summer,
they move to warmer river estuaries and
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coastal areas for molting and calving
(Muto et al., 2017). Annual migrations
can span over thousands of kilometers.
The residential Beaufort Sea
populations participate in short distance
movements within their range
throughout the year. Based on satellite
tags (Suydam et al., 2001) there is some
overlap in distribution with the eastern
Chukchi Sea beluga whale stock.
During the winter, eastern Chukchi
Sea belugas occur in offshore waters
associated with pack ice. In the spring,
they migrate to warmer coastal
estuaries, bays, and rivers where they
may molt (Finley 1982; Suydam 2009)
and give birth to and care for their
calves (Sergeant and Brodie 1969).
Eastern Chukchi Sea belugas move into
coastal areas, including Kasegaluk
Lagoon (outside of the Study Area), in
late June and animals are sighted in the
area until about mid-July (Frost and
Lowry 1990; Frost et al., 1993). Satellite
tags attached to eastern Chukchi Sea
belugas captured in Kaseguluk Lagoon
during the summer showed these
whales traveled 593 nm (1,100 km)
north of the Alaska coastline, into the
Canadian Beaufort Sea within three
months (Suydam et al., 2001). Satellite
telemetry data from 23 whales tagged
during 1998–2007 suggest variation in
movement patterns for different age
and/or sex classes during JulySeptember (Suydam et al., 2005). Adult
males used deeper waters and remained
there for the duration of the summer; all
belugas that moved into the Arctic
Ocean (north of 75° N) were males, and
males traveled through 90 percent pack
ice cover to reach deeper waters in the
Beaufort Sea and Arctic Ocean (79–80°
N) by late July/early August. Adult and
immature female belugas remained at or
near the shelf break in the south through
the eastern Bering Strait into the
northern Bering Sea, remaining north of
Saint Lawrence Island over the winter.
A whale tagged in the eastern Chukchi
Sea in 2007 overwintered in the waters
north of Saint Lawrence Island during
2007/2008 and moved to near King
Island in April and May before moving
north through the Bering Strait in late
May and early June (Suydam 2009).
Bearded Seal
Bearded seals are a boreoarctic
species with circumpolar distribution
(Burns 1967; Burns 1981; Burns and
Frost 1979; Fedoseev 1965; Johnson et
al., 1966; Kelly 1988a; Smith 1981).
Their normal range extends from the
Arctic Ocean (85° N) south to Sakhalin
Island (45° N) in the Pacific and south
to Hudson Bay (55° N) in the Atlantic
(Allen 1880; King 1983; Ognev 1935).
Bearded seals are widely distributed
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throughout the northern Bering,
Chukchi, and Beaufort Seas and are
most abundant north of the ice edge
zone (MacIntyre et al., 2013). Bearded
seals inhabit the seasonally ice-covered
seas of the Northern Hemisphere, where
they whelp and rear their pups and molt
their coats on the ice in the spring and
early summer. The overall summer
distribution is quite broad, with seals
rarely hauled out on land, and some
seals, mostly juveniles, may not follow
the ice northward but remain near the
coasts of Bering and Chukchi seas
(Burns 1967; Burns 1981; Heptner et al.,
Nelson 1981). As the ice forms again in
the fall and winter, most seals move
south with the advancing ice edge
through the Bering Strait into the Bering
Sea where they spend the winter
(Boveng and Cameron 2013; Burns and
Frost 1979; Cameron and Boveng 2007;
Cameron and Boveng 2009; Frost et al.,
2005; Frost et al., 2008). This southward
migration is less noticeable and
predictable than the northward
movements in late spring and early
summer (Burns 1981; Burns and Frost
1979; Kelly 1988a). During winter, the
central and northern parts of the Bering
Sea shelf have the highest densities of
bearded seals (Braham et al., 1981;
Burns 1981; Burns and Frost 1979; Fay
1974; Heptner et al., 1976; Nelson et al.,
1984). In late winter and early spring,
bearded seals are widely but not
uniformly distributed in the broken,
drifting pack ice ranging from the
Chukchi Sea south to the ice front in the
Bering Sea. In these areas, they tend to
avoid the coasts and areas of fast ice
(Burns 1967; Burns and Frost 1979).
Bearded seals along the Alaskan coast
tend to prefer areas where sea ice covers
70 to 90 percent of the surface, and are
most abundant 20 to 100 nautical miles
(nmi) (37 to 185 (km) offshore during
the spring season (Bengston et al., 2000;
Bengston et al., 2005; Simpkins et al.,
2003). In spring, bearded seals may also
concentrate in nearshore pack ice
habitats, where females give birth on the
most stable areas of ice (Reeves et al.,
2003) and generally prefer to be near
polynyas (areas of open water
surrounded by sea ice) and other natural
openings in the sea ice for breathing,
hauling out, and prey access (Nelson et
al., 1984; Stirling 1997). While molting
between April and August, bearded
seals spend substantially more time
hauled out than at other times of the
year (Reeves et al., 2002).
In their explorations of the Canada
Basin, Harwood et al. (2005) observed
bearded seals in waters of less than 656
ft (200 m) during the months from
August to September. These sightings
were east of 140° W. The Bureau of
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Ocean Energy Management conducted
an aerial survey from June through
October that covered the shallow
Beaufort and Chukchi Sea shelf waters,
and observed bearded seals from Point
Barrow to the border of Canada (Clarke
et al., 2014). The farthest from shore that
bearded seals were observed was the
waters of the continental slope.
On December 28, 2012, NMFS listed
both the Okhotsk and the Beringia
distinct population segments (DPSs) of
bearded seals as threatened under the
ESA (77 FR 76740). The Alaska stock of
bearded seals consists of only Beringia
DPS seals.
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Ringed Seal
Ringed seals are the most common
pinniped in the Study Area and have
wide distribution in seasonally and
permanently ice-covered waters of the
Northern Hemisphere (North Atlantic
Marine Mammal Commission 2004).
Throughout their range, ringed seals
have an affinity for ice-covered waters
and are well adapted to occupying both
shore-fast and pack ice (Kelly 1988c).
Ringed seals can be found further
offshore than other pinnipeds since they
can maintain breathing holes in ice
thickness greater than 6.6 ft (2 m)
(Smith and Stirling 1975). Breathing
holes are maintained by ringed seals’
sharp teeth and claws on their fore
flippers. They remain in contact with
ice most of the year and use it as a
platform for molting in late spring to
early summer, for pupping and nursing
in late winter to early spring, and for
resting at other times of the year (Muto
et al., 2017).
Ringed seals have at least two distinct
types of subnivean lairs: Haulout lairs
and birthing lairs (Smith and Stirling
1975). Haulout lairs are typically singlechambered and offer protection from
predators and cold weather. Birthing
lairs are larger, multi-chambered areas
that are used for pupping in addition to
protection from predators. Ringed seals
pup on both land-fast ice as well as
stable pack ice. Lentfer (1972) found
that ringed seals north of Barrow,
Alaska build their subnivean lairs on
the pack ice near pressure ridges. Since
subnivean lairs were found north of
Barrow, Alaska, in pack ice, they are
also assumed to be found within the sea
ice in the Study Area. Ringed seals
excavate subnivean lairs in drifts over
their breathing holes in the ice, in
which they rest, give birth, and nurse
their pups for 5–9 weeks during late
winter and spring (Chapskii 1940;
McLaren 1958; Smith and Stirling
1975). Snow depths of at least 20–26 in
(50–65 cm) are required for functional
birth lairs (Kelly 1988b; Lydersen 1998;
Lydersen and Gjertz 1986; Smith and
Stirling 1975), and such depths
typically are found only where 8–12 in
(20–30 cm) or more of snow has
accumulated on flat ice and then drifted
along pressure ridges or ice hummocks
(Hammill 2008; Lydersen et al., 1990;
Lydersen and Ryg 1991; Smith and
Lydersen 1991). Ringed seals are born
beginning in March, but the majority of
births occur in early April. About a
month after parturition, mating begins
in late April and early May.
In Alaska waters, during winter and
early spring when sea ice is at its
maximum extent, ringed seals are
abundant in the northern Bering Sea,
Norton and Kotzebue Sounds, and
throughout the Chukchi and Beaufort
seas (Frost 1985; Kelly 1988c). Passive
acoustic monitoring of ringed seals from
a high frequency recording package
deployed at a depth of 787 ft (240 m) in
the Chukchi Sea 65 nmi (120 km) northnorthwest of Barrow, Alaska detected
ringed seals in the area between midDecember and late May over the 4 year
study (Jones et al., 2014). With the onset
of fall freeze, ringed seal movements
become increasingly restricted and seals
will either move west and south with
the advancing ice pack with many seals
dispersing throughout the Chukchi and
Bering Seas, or remaining in the
Beaufort Sea (Crawford et al., 2012;
Frost and Lowry 1984; Harwood et al.,
2012). Kelly et al. (2010a) tracked home
ranges for ringed seals in the subnivean
period (using shore-fast ice); the size of
the home ranges varied from less than
1 up to 279 km2 (median is 0.62 km2 for
adult males and 0.65 km2 for adult
females). Most (94 percent) of the home
ranges were less than 3 km2 during the
subnivean period (Kelly et al., 2010a).
Near large polynyas, ringed seals
maintain ranges, up to 7,000 km2 during
winter and 2,100 km2 during spring
(Born et al., 2004). Some adult ringed
seals return to the same small home
ranges they occupied during the
previous winter (Kelly et al., 2010a).
The size of winter home ranges can,
however, vary by up to a factor of 10
depending on the amount of fast ice;
seal movements were more restricted
during winters with extensive fast ice,
and were much less restricted where
fast ice did not form at high levels
(Harwood et al., 2015).
Most taxonomists recognize five
subspecies of ringed seals. The Arctic
ringed seal subspecies occurs in the
Arctic Ocean and Bering Sea and is the
only stock that occurs in U.S. waters
(referred to as the Alaska stock). NMFS
listed the Arctic ringed seal subspecies
as threatened under the ESA on
December 28, 2012 (77 FR 76706),
primarily due to anticipated loss of sea
ice through the end of the 21st century.
Marine Mammal Hearing
Hearing is the most important sensory
modality for marine mammals
underwater, and exposure to
anthropogenic sound can have
deleterious effects. To appropriately
assess the potential effects of exposure
to sound, it is necessary to understand
the frequency ranges marine mammals
are able to hear. Current data indicate
that not all marine mammal species
have equal hearing capabilities (e.g.,
Richardson et al., 1995; Wartzok and
Ketten, 1999; Au and Hastings, 2008).
To reflect this, Southall et al. (2007)
recommended that marine mammals be
divided into functional hearing groups
based on directly measured or estimated
hearing ranges on the basis of available
behavioral response data, audiograms
derived using auditory evoked potential
techniques, anatomical modeling, and
other data. Note that no direct
measurements of hearing ability have
been successfully completed for
mysticetes (i.e., low-frequency
cetaceans). Subsequently, NMFS (2018)
described generalized hearing ranges for
these marine mammal hearing groups.
Generalized hearing ranges were chosen
based on the approximately 65 dB
threshold from the normalized
composite audiograms, with the
exception for lower limits for lowfrequency cetaceans where the lower
bound was deemed to be biologically
implausible and the lower bound from
Southall et al. (2007) retained. Marine
mammal hearing groups and their
associated hearing ranges are provided
in Table 4.
TABLE 4—MARINE MAMMAL HEARING GROUPS
[NMFS, 2018]
Generalized hearing
range *
Hearing group
Low-frequency (LF) cetaceans (baleen whales) ...................................................................................................................
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37249
TABLE 4—MARINE MAMMAL HEARING GROUPS—Continued
[NMFS, 2018]
Generalized hearing
range *
Hearing group
Mid-frequency (MF) cetaceans (dolphins, toothed whales, beaked whales, bottlenose whales) ........................................
High-frequency (HF) cetaceans (true porpoises, Kogia, river dolphins, cephalorhynchid, Lagenorhynchus cruciger & L.
australis).
Phocid pinnipeds (PW) (underwater) (true seals) .................................................................................................................
Otariid pinnipeds (OW) (underwater) (sea lions and fur seals) ............................................................................................
150 Hz to 160 kHz.
275 Hz to 160 kHz.
50 Hz to 86 kHz.
60 Hz to 39 kHz.
* Represents the generalized hearing range for the entire group as a composite (i.e., all species within the group), where individual species’
hearing ranges are typically not as broad. Generalized hearing range chosen based on ∼65 dB threshold from normalized composite audiogram,
with the exception for lower limits for LF cetaceans (Southall et al. 2007) and PW pinniped (approximation).
The pinniped functional hearing
group was modified from Southall et al.
(2007) on the basis of data indicating
that phocid species have consistently
demonstrated an extended frequency
range of hearing compared to otariids,
especially in the higher frequency range
(Hemila¨ et al., 2006; Kastelein et al.,
2009; Reichmuth and Holt, 2013).
For more detail concerning these
groups and associated frequency ranges,
please see NMFS (2018) for a review of
available information. Three marine
mammal species (one cetacean and two
pinniped (both phocid) species) have
the reasonable potential to co-occur
with the proposed survey activities.
Please refer to Table 3. Beluga whales
are classified as mid-frequency
cetaceans.
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Potential Effects of Specified Activities
on Marine Mammals and Their Habitat
This section includes a summary and
discussion of the ways that components
of the specified activity may impact
marine mammals and their habitat. The
Estimated Take by Incidental
Harassment section later in this
document includes a quantitative
analysis of the number of individuals
that are expected to be taken by this
activity. The Negligible Impact Analysis
and Determination section considers the
content of this section, the Estimated
Take by Incidental Harassment section,
and the Proposed Mitigation section, to
draw conclusions regarding the likely
impacts of these activities on the
reproductive success or survivorship of
individuals and how those impacts on
individuals are likely to impact marine
mammal species or stocks.
Description of Sound Sources
Here, we first provide background
information on marine mammal hearing
before discussing the potential effects of
the use of active acoustic sources on
marine mammals.
Sound travels in waves, the basic
components of which are frequency,
wavelength, velocity, and amplitude.
Frequency is the number of pressure
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waves that pass by a reference point per
unit of time and is measured in Hz or
cycles per second. Wavelength is the
distance between two peaks of a sound
wave; lower frequency sounds have
longer wavelengths than higher
frequency sounds and attenuate
(decrease) more rapidly in shallower
water. Amplitude is the height of the
sound pressure wave or the ‘loudness’
of a sound and is typically measured
using the dB scale. A dB is the ratio
between a measured pressure (with
sound) and a reference pressure (sound
at a constant pressure, established by
scientific standards). It is a logarithmic
unit that accounts for large variations in
amplitude; therefore, relatively small
changes in dB ratings correspond to
large changes in sound pressure. When
referring to sound pressure levels (SPLs;
the sound force per unit area), sound is
referenced in the context of underwater
sound pressure to 1 mPa. One pascal is
the pressure resulting from a force of
one newton exerted over an area of one
square meter. The source level (SL)
represents the sound level at a distance
of 1 m from the source (referenced to 1
mPa). The received level is the sound
level at the listener’s position. Note that
all underwater sound levels in this
document are referenced to a pressure of
1 mPa.
Root mean square (rms) is the
quadratic mean sound pressure over the
duration of an impulse. RMS is
calculated by squaring all of the sound
amplitudes, averaging the squares, and
then taking the square root of the
average (Urick 1983). RMS accounts for
both positive and negative values;
squaring the pressures makes all values
positive so that they may be accounted
for in the summation of pressure levels
(Hastings and Popper 2005). This
measurement is often used in the
context of discussing behavioral effects,
in part because behavioral effects,
which often result from auditory cues,
may be better expressed through
averaged units than by peak pressures.
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When underwater objects vibrate or
activity occurs, sound-pressure waves
are created. These waves alternately
compress and decompress the water as
the sound wave travels. Underwater
sound waves radiate in all directions
away from the source (similar to ripples
on the surface of a pond), except in
cases where the source is directional.
The compressions and decompressions
associated with sound waves are
detected as changes in pressure by
aquatic life and man-made sound
receptors such as hydrophones.
Even in the absence of sound from the
specified activity, the underwater
environment is typically loud due to
ambient sound. Ambient sound is
defined as environmental background
sound levels lacking a single source or
point (Richardson et al., 1995), and the
sound level of a region is defined by the
total acoustical energy being generated
by known and unknown sources. These
sources may include physical (e.g.,
waves, earthquakes, ice, atmospheric
sound), biological (e.g., sounds
produced by marine mammals, fish, and
invertebrates), and anthropogenic sound
(e.g., vessels, dredging, aircraft,
construction). A number of sources
contribute to ambient sound, including
the following (Richardson et al., 1995):
• Wind and waves: The complex
interactions between wind and water
surface, including processes such as
breaking waves and wave-induced
bubble oscillations and cavitation, are a
main source of naturally occurring
ambient noise for frequencies between
200 Hz and 50 kHz (Mitson, 1995).
Under sea ice, noise generated by ice
deformation and ice fracturing may be
caused by thermal, wind, drift and
current stresses (Roth et al., 2012);
• Precipitation: Sound from rain and
hail impacting the water surface can
become an important component of total
noise at frequencies above 500 Hz, and
possibly down to 100 Hz during quiet
times. In the ice-covered study area,
precipitation is unlikely to impact
ambient sound;
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• Biological: Marine mammals can
contribute significantly to ambient noise
levels, as can some fish and shrimp. The
frequency band for biological
contributions is from approximately 12
Hz to over 100 kHz; and
• Anthropogenic: Sources of ambient
noise related to human activity include
transportation (surface vessels and
aircraft), dredging and construction, oil
and gas drilling and production, seismic
surveys, sonar, explosions, and ocean
acoustic studies. Shipping noise
typically dominates the total ambient
noise for frequencies between 20 and
300 Hz. In general, the frequencies of
anthropogenic sounds are below 1 kHz
and, if higher frequency sound levels
are created, they attenuate rapidly
(Richardson et al., 1995). Sound from
identifiable anthropogenic sources other
than the activity of interest (e.g., a
passing vessel) is sometimes termed
background sound, as opposed to
ambient sound. Anthropogenic sources
are unlikely to significantly contribute
to ambient underwater noise during the
late winter and early spring in the study
area as most anthropogenic activities
will not be active due to ice cover (e.g.
seismic surveys, shipping) (Roth et al.,
2012).
The sum of the various natural and
anthropogenic sound sources at any
given location and time—which
comprise ‘‘ambient’’ or ‘‘background’’
sound—depends not only on the source
levels (as determined by current
weather conditions and levels of
biological and shipping activity) but
also on the ability of sound to propagate
through the environment. In turn, sound
propagation is dependent on the
spatially and temporally varying
properties of the water column and sea
floor, and is frequency-dependent. As a
result of the dependence on a large
number of varying factors, ambient
sound levels can be expected to vary
widely over both coarse and fine spatial
and temporal scales. Sound levels at a
given frequency and location can vary
by 10–20 dB from day to day
(Richardson et al., 1995). The result is
that, depending on the source type and
its intensity, sound from the specified
activity may be a negligible addition to
the local environment or could form a
distinctive signal that may affect marine
mammals.
Underwater sounds fall into one of
two general sound types: Impulsive and
non-impulsive (defined in the following
paragraphs). The distinction between
these two sound types is important
because they have differing potential to
cause physical effects, particularly with
regard to hearing (e.g., Ward, 1997 in
Southall et al., 2007). Please see
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Southall et al., (2007) for an in-depth
discussion of these concepts.
Impulsive sound sources (e.g.,
explosions, gunshots, sonic booms,
impact pile driving) produce signals
that are brief (typically considered to be
less than one second), broadband, atonal
transients (ANSI 1986; Harris 1998;
NIOSH 1998; ISO 2003; ANSI 2005) and
occur either as isolated events or
repeated in some succession. Impulsive
sounds are all characterized by a
relatively rapid rise from ambient
pressure to a maximal pressure value
followed by a rapid decay period that
may include a period of diminishing,
oscillating maximal and minimal
pressures, and generally have an
increased capacity to induce physical
injury as compared with sounds that
lack these features.
Non-impulsive sounds can be tonal,
narrowband, or broadband, brief or
prolonged, and may be either
continuous or non-continuous (ANSI
1995; NIOSH 1998). Some of these nonimpulsive sounds can be transient
signals of short duration but without the
essential properties of pulses (e.g., rapid
rise time). Examples of non-impulsive
sounds include those produced by
vessels, aircraft, machinery operations
such as drilling or dredging, vibratory
pile driving, and active sonar sources
that intentionally direct a sound signal
at a target that is reflected back in order
to discern physical details about the
target. These active sources are used in
navigation, military training and testing,
and other research activities such as the
activities planned by ONR as part of the
proposed action. Icebreaking is also
considered a non-impulsive sound. The
duration of such sounds, as received at
a distance, can be greatly extended in a
highly reverberant environment.
Acoustic Impacts
Please refer to the information given
previously regarding sound,
characteristics of sound types, and
metrics used in this document.
Anthropogenic sounds cover a broad
range of frequencies and sound levels
and can have a range of highly variable
impacts on marine life, from none or
minor to potentially severe responses,
depending on received levels, duration
of exposure, behavioral context, and
various other factors. The potential
effects of underwater sound from active
acoustic sources can potentially result
in one or more of the following:
temporary or permanent hearing
impairment, non-auditory physical or
physiological effects, behavioral
disturbance, stress, and masking
(Richardson et al., 1995; Gordon et al.,
2004; Nowacek et al., 2007; Southall et
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al., 2007; Gotz et al., 2009). The degree
of effect is intrinsically related to the
signal characteristics, received level,
distance from the source, and duration
of the sound exposure. In general,
sudden, high level sounds can cause
hearing loss, as can longer exposures to
lower level sounds. Temporary or
permanent loss of hearing will occur
almost exclusively for noise within an
animal’s hearing range. In this section,
we first describe specific manifestations
of acoustic effects before providing
discussion specific to the proposed
activities in the next section.
Permanent Threshold Shift—Marine
mammals exposed to high-intensity
sound, or to lower-intensity sound for
prolonged periods, can experience
hearing threshold shift (TS), which is
the loss of hearing sensitivity at certain
frequency ranges (Finneran 2015). TS
can be permanent (PTS), in which case
the loss of hearing sensitivity is not
fully recoverable, or temporary (TTS), in
which case the animal’s hearing
threshold would recover over time
(Southall et al., 2007). Repeated sound
exposure that leads to TTS could cause
PTS. In severe cases of PTS, there can
be total or partial deafness, while in
most cases the animal has an impaired
ability to hear sounds in specific
frequency ranges (Kryter 1985).
When PTS occurs, there is physical
damage to the sound receptors in the ear
(i.e., tissue damage), whereas TTS
represents primarily tissue fatigue and
is reversible (Southall et al., 2007). In
addition, other investigators have
suggested that TTS is within the normal
bounds of physiological variability and
tolerance and does not represent
physical injury (e.g., Ward, 1997).
Therefore, NMFS does not consider TTS
to constitute auditory injury.
Relationships between TTS and PTS
thresholds have not been studied in
marine mammals—PTS data exists only
for a single harbor seal (Kastak et al.,
2008)—but are assumed to be similar to
those in humans and other terrestrial
mammals. PTS typically occurs at
exposure levels at least several decibels
above (a 40-dB threshold shift
approximates PTS onset; e.g., Kryter et
al., 1966; Miller, 1974) that inducing
mild TTS (a 6-dB threshold shift
approximates TTS onset; e.g., Southall
et al., 2007). Based on data from
terrestrial mammals, a precautionary
assumption is that the PTS thresholds
for impulse sounds (such as impact pile
driving pulses as received close to the
source) are at least six dB higher than
the TTS threshold on a peak-pressure
basis and PTS cumulative sound
exposure level (SEL) thresholds are 15
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to 20 dB higher than TTS cumulative
SEL thresholds (Southall et al., 2007).
Temporary Threshold Shift—TTS is
the mildest form of hearing impairment
that can occur during exposure to sound
(Kryter, 1985). While experiencing TTS,
the hearing threshold rises, and a sound
must be at a higher level in order to be
heard. In terrestrial and marine
mammals, TTS can last from minutes or
hours to days (in cases of strong TTS).
In many cases, hearing sensitivity
recovers rapidly after exposure to the
sound ends.
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. 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.
Currently, TTS data only exist for four
species of cetaceans (bottlenose dolphin
(Tursiops truncatus), beluga whale,
harbor porpoise, and Yangtze finless
porpoise (Neophocoena asiaeorientalis))
and three species of pinnipeds (northern
elephant seal (Mirounga angustirostris),
harbor seal, and California sea lion
(Zalophus californianus)) exposed to a
limited number of sound sources (i.e.,
mostly tones and octave-band noise) in
laboratory settings (Finneran 2015). TTS
was not observed in trained spotted and
ringed seals exposed to impulsive noise
at levels matching previous predictions
of TTS onset (Reichmuth et al., 2016).
In general, harbor seals and harbor
porpoises have a lower TTS onset than
other measured pinniped or cetacean
species. Additionally, the existing
marine mammal TTS data come from a
limited number of individuals within
these species. There are no data
available on noise-induced hearing loss
for mysticetes. For summaries of data on
TTS in marine mammals or for further
discussion of TTS onset thresholds,
please see Southall et al. (2007),
Finneran and Jenkins (2012), and
Finneran (2015).
Behavioral effects—Behavioral
disturbance may include a variety of
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effects, including subtle changes in
behavior (e.g., minor or brief avoidance
of an area or changes in vocalizations),
more conspicuous changes in similar
behavioral activities, and more
sustained and/or potentially severe
reactions, such as displacement from or
abandonment of high-quality habitat.
Behavioral responses to sound are
highly variable and context-specific and
any reactions depend on numerous
intrinsic and extrinsic factors (e.g.,
species, state of maturity, experience,
current activity, reproductive state,
auditory sensitivity, time of day), as
well as the interplay between factors
(e.g., Richardson et al., 1995; Wartzok et
al., 2003; Southall et al., 2007; Weilgart,
2007; Archer et al., 2010). Behavioral
reactions can vary not only among
individuals but also within an
individual, depending on previous
experience with a sound source,
context, and numerous other factors
(Ellison et al., 2012), and can vary
depending on characteristics associated
with the sound source (e.g., whether it
is moving or stationary, number of
sources, distance from the source).
Please see Appendices B–C of Southall
et al. (2007) for a review of studies
involving marine mammal behavioral
responses to sound.
Habituation can occur when an
animal’s response to a stimulus wanes
with repeated exposure, usually in the
absence of unpleasant associated events
(Wartzok et al., 2003). Animals are most
likely to habituate to sounds that are
predictable and unvarying. It is
important to note that habituation is
appropriately considered as a
‘‘progressive reduction in response to
stimuli that are perceived as neither
aversive nor beneficial,’’ rather than as,
more generally, moderation in response
to human disturbance (Bejder et al.,
2009). The opposite process is
sensitization, when an unpleasant
experience leads to subsequent
responses, often in the form of
avoidance, at a lower level of exposure.
As noted, behavioral state may affect the
type of response. For example, animals
that are resting may show greater
behavioral change in response to
disturbing sound levels than animals
that are highly motivated to remain in
an area for feeding (Richardson et al.
1995; NRC 2003; Wartzok et al. 2003).
Controlled experiments with captive
marine mammals have showed
pronounced behavioral reactions,
including avoidance of loud sound
sources (Ridgway et al. 1997; Finneran
et al. 2003). Observed responses of wild
marine mammals to loud impulsive
sound sources (typically seismic airguns
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37251
or acoustic harassment devices) have
been varied but often consist of
avoidance behavior or other behavioral
changes suggesting discomfort (Morton
and Symonds 2002; see also Richardson
et al., 1995; Nowacek et al., 2007).
Available studies show wide variation
in response to underwater sound;
therefore, it is difficult to predict
specifically how any given sound in a
particular instance might affect marine
mammals perceiving the signal. If a
marine mammal does react briefly to an
underwater sound by changing its
behavior or moving a small distance, the
impacts of the change are unlikely to be
significant to the individual, let alone
the stock or population. However, if a
sound source displaces marine
mammals from an important feeding or
breeding area for a prolonged period,
impacts on individuals and populations
could be significant (e.g., Lusseau and
Bejder 2007; Weilgart 2007; NRC 2003).
However, there are broad categories of
potential response, which we describe
in greater detail here, that include
alteration of dive behavior, alteration of
foraging behavior, effects to breathing,
interference with or alteration of
vocalization, avoidance, and flight.
Changes in dive behavior can vary
widely, and may consist of increased or
decreased dive times and surface
intervals as well as changes in the rates
of ascent and descent during a dive (e.g.,
Frankel and Clark 2000; Costa et al.,
2003; Ng and Leung, 2003; Nowacek et
al., 2004; Goldbogen et al., 2013).
Variations in dive behavior may reflect
interruptions in biologically significant
activities (e.g., foraging) or they may be
of little biological significance. The
impact of an alteration to dive behavior
resulting from an acoustic exposure
depends on what the animal is doing at
the time of the exposure and the type
and magnitude of the response.
Disruption of feeding behavior can be
difficult to correlate with anthropogenic
sound exposure, so it is usually inferred
by observed displacement from known
foraging areas, the appearance of
secondary indicators (e.g., bubble nets
or sediment plumes), or changes in dive
behavior. As for other types of
behavioral response, the frequency,
duration, and temporal pattern of signal
presentation, as well as differences in
species sensitivity, are likely
contributing factors to differences in
response in any given circumstance
(e.g., Croll et al., 2001; Nowacek et al.;
2004; Madsen et al., 2006; Yazvenko et
al., 2007). A determination of whether
foraging disruptions incur fitness
consequences would require
information on or estimates of the
energetic requirements of the affected
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individuals and the relationship
between prey availability, foraging effort
and success, and the life history stage of
the animal.
Variations in respiration naturally
vary with different behaviors and
alterations to breathing rate as a
function of acoustic exposure can be
expected to co-occur with other
behavioral reactions, such as a flight
response or an alteration in diving.
However, respiration rates in and of
themselves may be representative of
annoyance or an acute stress response.
Various studies have shown that
respiration rates may either be
unaffected or could increase, depending
on the species and signal characteristics,
again highlighting the importance in
understanding species differences in the
tolerance of underwater noise when
determining the potential for impacts
resulting from anthropogenic sound
exposure (e.g., Kastelein et al., 2001,
2005b, 2006; Gailey et al., 2007).
Marine mammals vocalize for
different purposes and across multiple
modes, such as whistling, echolocation
click production, calling, and singing.
Changes in vocalization behavior in
response to anthropogenic noise can
occur for any of these modes and may
result from a need to compete with an
increase in background noise or may
reflect increased vigilance or a startle
response. For example, in the presence
of potentially masking signals,
humpback whales and killer whales
have been observed to increase the
length of their songs (Miller et al., 2000;
Fristrup et al., 2003; Foote et al., 2004),
while right whales have been observed
to shift the frequency content of their
calls upward while reducing the rate of
calling in areas of increased
anthropogenic noise (Parks et al.,
2007b). In some cases, animals may
cease sound production during
production of aversive signals (Bowles
et al., 1994).
Avoidance is the displacement of an
individual from an area or migration
path as a result of the presence of a
sound or other stressors, and is one of
the most obvious manifestations of
disturbance in marine mammals
(Richardson et al., 1995). For example,
gray whales are known to change
direction—deflecting from customary
migratory paths—in order to avoid noise
from seismic surveys (Malme et al.,
1984). Avoidance may be short-term,
with animals returning to the area once
the noise has ceased (e.g., Bowles et al.,
1994; Goold, 1996; Morton and
Symonds, 2002; Gailey et al., 2007).
Longer-term displacement is possible,
however, which may lead to changes in
abundance or distribution patterns of
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the affected species in the affected
region if habituation to the presence of
the sound does not occur (e.g.,
Blackwell et al., 2004; Bejder et al.,
2006).
A flight response is a dramatic change
in normal movement to a directed and
rapid movement away from the
perceived location of a sound source.
The flight response differs from other
avoidance responses in the intensity of
the response (e.g., directed movement,
rate of travel). Relatively little
information on flight responses of
marine mammals to anthropogenic
signals exist, although observations of
flight responses to the presence of
predators have occurred (Connor and
Heithaus 1996). The result of a flight
response could range from brief,
temporary exertion and displacement
from the area where the signal provokes
flight to, in extreme cases, marine
mammal strandings (Evans and England
2001). However, it should be noted that
response to a perceived predator does
not necessarily invoke flight (Ford and
Reeves 2008), and whether individuals
are solitary or in groups may influence
the response.
Behavioral disturbance can also
impact marine mammals in more subtle
ways. Increased vigilance may result in
costs related to diversion of focus and
attention (i.e., when a response consists
of increased vigilance, it may come at
the cost of decreased attention to other
critical behaviors such as foraging or
resting). These effects have generally not
been demonstrated for marine
mammals, but studies involving fish
and terrestrial animals have shown that
increased vigilance may substantially
reduce feeding rates (e.g., Beauchamp
and Livoreil,1997; Fritz et al., 2002;
Purser and Radford 2011). In addition,
chronic disturbance can cause
population declines through reduction
of fitness (e.g., decline in body
condition) and subsequent reduction in
reproductive success, survival, or both
(e.g., Harrington and Veitch 1992; Daan
et al., 1996; Bradshaw et al., 1998).
However, Ridgway et al. (2006) reported
that increased vigilance in bottlenose
dolphins exposed to sound over a fiveday period did not cause any sleep
deprivation or stress effects.
Many animals perform vital functions,
such as feeding, resting, traveling, and
socializing, on a diel cycle (24-hour
cycle). Disruption of such functions
resulting from reactions to stressors
such as sound exposure are more likely
to be significant if they last more than
one diel cycle or recur on subsequent
days (Southall et al., 2007).
Consequently, a behavioral response
lasting less than one day and not
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recurring on subsequent days is not
considered particularly severe unless it
could directly affect reproduction or
survival (Southall et al., 2007). Note that
there is a difference between multi-day
substantive behavioral reactions and
multi-day anthropogenic activities. For
example, just because an activity lasts
for multiple days does not necessarily
mean that individual animals are either
exposed to activity-related stressors for
multiple days or, further, exposed in a
manner resulting in sustained multi-day
substantive behavioral responses.
For non-impulsive sounds (i.e.,
similar to the sources used during the
proposed action), data suggest that
exposures of pinnipeds to sources
between 90 and 140 dB re 1 mPa do not
elicit strong behavioral responses; no
data were available for exposures at
higher received levels for Southall et al.
(2007) to include in the severity scale
analysis. Reactions of harbor seals were
the only available data for which the
responses could be ranked on the
severity scale. For reactions that were
recorded, the majority (17 of 18
individuals/groups) were ranked on the
severity scale as a 4 (defined as
moderate change in movement, brief
shift in group distribution, or moderate
change in vocal behavior) or lower; the
remaining response was ranked as a 6
(defined as minor or moderate
avoidance of the sound source).
Additional data on hooded seals
(Cystophora cristata) indicate avoidance
responses to signals above 160–170 dB
re 1 mPa (Kvadsheim et al., 2010), and
data on grey (Halichoerus grypus) and
harbor seals indicate avoidance
response at received levels of 135–144
dB re 1 mPa (Go¨tz et al., 2010). In each
instance where food was available,
which provided the seals motivation to
remain near the source, habituation to
the signals occurred rapidly. In the same
study, it was noted that habituation was
not apparent in wild seals where no
food source was available (Go¨tz et al.
2010). This implies that the motivation
of the animal is necessary to consider in
determining the potential for a reaction.
In one study aimed to investigate the
under-ice movements and sensory cues
associated with under-ice navigation of
ice seals, acoustic transmitters (60–69
kHz at 159 dB re 1 mPa at 1 m) were
attached to ringed seals (Wartzok et al.,
1992a; Wartzok et al., 1992b). An
acoustic tracking system then was
installed in the ice to receive the
acoustic signals and provide real-time
tracking of ice seal movements.
Although the frequencies used in this
study are at the upper limit of ringed
seal hearing, the ringed seals appeared
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unaffected by the acoustic
transmissions, as they were able to
maintain normal behaviors (e.g., finding
breathing holes).
Seals exposed to non-impulsive
sources with a received sound pressure
level within the range of calculated
exposures (142–193 dB re 1 mPa), have
been shown to change their behavior by
modifying diving activity and avoidance
of the sound source (Go¨tz et al., 2010;
Kvadsheim et al., 2010). Although a
minor change to a behavior may occur
as a result of exposure to the sources in
the proposed action, these changes
would be within the normal range of
behaviors for the animal (e.g., the use of
a breathing hole further from the source,
rather than one closer to the source,
would be within the normal range of
behavior) (Kelly et al. 1988).
Some behavioral response studies
have been conducted on odontocete
responses to sonar. In studies that
examined sperm whales (Physeter
macrocephalus) and false killer whales
(Pseudorca crassidens) (both in the midfrequency cetacean hearing group), the
marine mammals showed temporary
cessation of calling and avoidance of
sonar sources (Akamatsu et al., 1993;
Watkins and Schevill 1975). Sperm
whales resumed calling and
communication approximately two
minutes after the pings stopped
(Watkins and Schevill 1975). False killer
whales moved away from the sound
source but returned to the area between
0 and 10 minutes after the end of
transmissions (Akamatsu et al., 1993).
Many of the contextual factors resulting
from the behavioral response studies
(e.g., close approaches by multiple
vessels or tagging) would not occur
during the proposed action. Odontocete
behavioral responses to acoustic
transmissions from non-impulsive
sources used during the proposed action
would likely be a result of the animal’s
behavioral state and prior experience
rather than external variables such as
ship proximity; thus, if significant
behavioral responses occur they would
likely be short term. In fact, no
significant behavioral responses such as
panic, stranding, or other severe
reactions have been observed during
monitoring of actual training exercises
(Department of the Navy 2011, 2014;
Smultea and Mobley 2009; Watwood et
al., 2012).
Icebreaking noise has the potential to
disturb marine mammals and elicit an
alerting, avoidance, or other behavioral
reaction (Huntington et al., 2015; Pirotta
et al., 2015; Williams et al., 2014).
Icebreaking in fast ice during the spring
can cause behavioral reactions in beluga
whales. However, icebreaking
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associated with the proposed action
would only occur from August through
October, which lessens the probability
of a whale encountering the vessel (in
comparison to other sources in the
proposed action that would be active
year-round).
Ringed seals and bearded seals on
pack ice showed various behaviors
when approached by an icebreaking
vessel. A majority of seals dove
underwater when the ship was within
0.5 nautical miles (0.93 km) while
others remained on the ice. However, as
icebreaking vessels came closer to the
seals, most dove underwater. Ringed
seals have also been observed foraging
in the wake of an icebreaking vessel
(Richardson et al., 1995). In studies by
Alliston (1980; 1981), there was no
observed change in the density of ringed
seals in areas that had been subject to
icebreaking. Alternatively, ringed seals
may have preferentially established
breathing holes in the ship tracks after
the icebreaker moved through the area.
Due to the time of year of the activity
(August through October), ringed seals
are not expected to be within the
subnivean lairs nor pupping (Chapskii
1940; McLaren 1958; Smith and Stirling
1975).
Adult ringed seals spend up to 20
percent of the time in subnivean lairs
during the winter season (Kelly et al.,
2010a). Ringed seal pups spend about
50 percent of their time in the lair
during the nursing period (Lydersen and
Hammill 1993). During the warm season
both bearded seals and ringed seals haul
out on the ice. In a study of ringed seal
haulout activity by Born et al. (2002),
ringed seals spent 25–57 percent of their
time hauled out in June which is during
their molting season. Bearded seals also
spend a large amount of time hauled out
during the molting season between
April and August (Reeves et al., 2002).
Ringed seal lairs are typically used by
individual seals (haulout lairs) or by a
mother with a pup (birthing lairs); large
lairs used by many seals for hauling out
are rare (Smith and Stirling 1975). If the
non-impulsive acoustic transmissions
are heard and are perceived as a threat,
ringed seals within subnivean lairs
could react to the sound in a similar
fashion to their reaction to other threats,
such as polar bears (their primary
predators), although the type of sound
would be novel to them. Responses of
ringed seals to a variety of humaninduced sounds (e.g., helicopter noise,
snowmobiles, dogs, people, and seismic
activity) have been variable; some seals
entered the water and some seals
remained in the lair. However, in all
instances in which observed seals
departed lairs in response to noise
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disturbance, they subsequently
reoccupied the lair (Kelly et al., 1988).
Ringed seal mothers have a strong
bond with their pups and may
physically move their pups from the
birth lair to an alternate lair to avoid
predation, sometimes risking their lives
to defend their pups from potential
predators (Smith 1987). If a ringed seal
mother perceives the proposed acoustic
sources as a threat, the network of
multiple birth and haulout lairs allows
the mother and pup to move to a new
lair (Smith and Hammill 1981; Smith
and Stirling 1975). The acoustic sources
and icebreaking noise from this
proposed action are not likely to impede
a ringed seal from finding a breathing
hole or lair, as captive seals have been
found to primarily use vision to locate
breathing holes and no effect to ringed
seal vision would occur from the
acoustic disturbance (Elsner et al., 1989;
Wartzok et al., 1992a). It is anticipated
that a ringed seal would be able to
relocate to a different breathing hole
relatively easily without impacting their
normal behavior patterns.
Stress responses—An animal’s
perception of a threat may be sufficient
to trigger stress responses consisting of
some combination of behavioral
responses, autonomic nervous system
responses, neuroendocrine responses, or
immune responses (e.g., Seyle 1950;
Moberg 2000). In many cases, an
animal’s first and sometimes most
economical (in terms of energetic costs)
response is behavioral avoidance of the
potential stressor. Autonomic nervous
system responses to stress typically
involve changes in heart rate, blood
pressure, and gastrointestinal activity.
These responses have a relatively short
duration and may or may not have a
significant long-term effect on an
animal’s fitness.
Neuroendocrine stress responses often
involve the hypothalamus-pituitaryadrenal 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,
altered metabolism, reduced immune
competence, and behavioral disturbance
(e.g., Moberg, 1987; Blecha, 2000).
Increases in the circulation of
glucocorticoids are also equated with
stress (Romano et al., 2004).
The primary distinction between
stress (which is adaptive and does not
normally place an animal at risk) and
‘‘distress’’ is the cost of the response.
During a stress response, an animal uses
glycogen stores that can be quickly
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replenished once the stress is alleviated.
In such circumstances, the cost of the
stress response would not pose serious
fitness consequences. 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
functions. This state of distress will last
until the animal replenishes its
energetic reserves sufficient to restore
normal function.
Relationships between these
physiological mechanisms, animal
behavior, and the costs of stress
responses are well-studied through
controlled experiments and for both
laboratory and free-ranging animals
(e.g., Holberton et al., 1996; Hood et al.,
1998; Jessop et al., 2003; Krausman et
al., 2004; Lankford et al., 2005). Stress
responses due to exposure to
anthropogenic sounds or other stressors
and their effects on marine mammals
have also been reviewed (Fair and
Becker, 2000; Romano et al., 2002b)
and, more rarely, studied in wild
populations (e.g., Romano et al., 2002a).
These and other studies lead to a
reasonable expectation that some
marine mammals will experience
physiological stress responses upon
exposure to acoustic stressors and that
it is possible that some of these would
be classified as ‘‘distress.’’ In addition,
any animal experiencing TTS would
likely also experience stress responses
(NRC, 2003).
Auditory masking—Sound can
disrupt behavior through masking, or
interfering with, an animal’s ability to
detect, recognize, or discriminate
between acoustic signals of interest (e.g.,
those used for intraspecific
communication and social interactions,
prey detection, predator avoidance,
navigation) (Richardson et al., 1995).
Masking occurs when the receipt of a
sound is interfered with by another
coincident sound at similar frequencies
and at similar or higher intensity, and
may occur whether the sound is natural
(e.g., snapping shrimp, wind, waves,
precipitation) or anthropogenic (e.g.,
shipping, sonar, seismic exploration) in
origin. The ability of a noise source to
mask biologically important sounds
depends on the characteristics of both
the noise source and the signal of
interest (e.g., signal-to-noise ratio,
temporal variability, direction), in
relation to each other and to an animal’s
hearing abilities (e.g., sensitivity,
frequency range, critical ratios,
frequency discrimination, directional
discrimination, age or TTS hearing loss),
and existing ambient noise and
propagation conditions.
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Under certain circumstances, marine
mammals experiencing significant
masking could also be impaired from
maximizing their performance fitness in
survival and reproduction. Therefore,
when the coincident (masking) sound is
anthropogenic, it may be considered
harassment when disrupting or altering
critical behaviors. It is important to
distinguish TTS and PTS, which persist
after the sound exposure, from masking,
which occurs during the sound
exposure. Because masking (without
resulting in TS) is not associated with
abnormal physiological function, it is
not considered a physiological effect,
but rather a potential behavioral effect.
The frequency range of the potentially
masking sound is important in
determining any potential behavioral
impacts. For example, low-frequency
signals may have less effect on highfrequency echolocation sounds
produced by odontocetes but are more
likely to affect detection of mysticete
communication calls and other
potentially important natural sounds
such as those produced by surf and
some prey species. The masking of
communication signals by
anthropogenic noise may be considered
as a reduction in the communication
space of animals (e.g., Clark et al., 2009)
and may result in energetic or other
costs as animals change their
vocalization behavior (e.g., Miller et al.,
2000; Foote et al., 2004; Parks et al.,
2007b; Di Iorio and Clark, 2009; Holt et
al., 2009). Masking can be reduced in
situations where the signal and noise
come from different directions
(Richardson et al., 1995), through
amplitude modulation of the signal, or
through other compensatory behaviors
(Houser and Moore, 2014). Masking can
be tested directly in captive species
(e.g., Erbe, 2008), but in wild
populations it must be either modeled
or inferred from evidence of masking
compensation. There are few studies
addressing real-world masking sounds
likely to be experienced by marine
mammals in the wild (e.g., Branstetter et
al., 2013).
Masking affects both senders and
receivers of acoustic signals and can
potentially have long-term chronic
effects on marine mammals at the
population level as well as at the
individual level. Low-frequency
ambient sound levels have increased by
as much as 20 dB (more than three times
in terms of SPL) in the world’s ocean
from pre-industrial periods, with most
of the increase from distant commercial
shipping (Hildebrand 2009). All
anthropogenic sound sources, but
especially chronic and lower-frequency
signals (e.g., from vessel traffic),
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contribute to elevated ambient sound
levels, thus intensifying masking.
Potential Effects on Prey—The marine
mammal species in the study area feed
on marine invertebrates and fish.
Studies of sound energy effects on
invertebrates are few, and primarily
identify behavioral responses. It is
expected that most marine invertebrates
would not sense the frequencies of the
acoustic transmissions from the acoustic
sources associated with the proposed
action. Although acoustic sources used
during the proposed action may briefly
impact individuals, intermittent
exposures to non-impulsive acoustic
sources are not expected to impact
survival, growth, recruitment, or
reproduction of widespread marine
invertebrate populations. Impacts to
invertebrates from icebreaking noise is
unknown, but it is likely that some
species including crustaceans and
cephalopods would be able to perceive
the low frequency sounds generated
from icebreaking. Icebreaking associated
with the proposed action would be
short-term and temporary as the vessel
moves through an area, and it is not
anticipated that this short-term noise
would result in significant harm, nor is
it expected to result in more than a
temporary behavioral reaction of marine
invertebrates in the vicinity of the
icebreaking event.
The fish species residing in the study
area include those that are closely
associated with the deep ocean habitat
of the Beaufort Sea. Nearly 250 marine
fish species have been described in the
Arctic, excluding the larger parts of the
sub-Arctic Bering, Barents, and
Norwegian Seas (Mecklenburg et al.,
2011). However, only about 30 are
known to occur in the Arctic waters of
the Beaufort Sea (Christiansen and Reist
2013). Although hearing capability data
only exist for fewer than 100 of the
32,000 named fish species, current data
suggest that most species of fish detect
sounds from 50 to 100 Hz, with few fish
hearing sounds above 4 kHz (Popper
2008). It is believed that most fish have
the best hearing sensitivity from 100 to
400 Hz (Popper 2003). Fish species in
the study area are expected to hear the
low-frequency sources associated with
the proposed action, but most are not
expected to detect sound from the midfrequency sources. Human generated
sound could alter the behavior of a fish
in a manner than would affect its way
of living, such as where it tries to locate
food or how well it could find a mate.
Behavioral responses to loud noise
could include a startle response, such as
the fish swimming away from the
source, the fish ‘‘freezing’’ and staying
in place, or scattering (Popper 2003).
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Icebreaking noise has the potential to
expose fish to both sound and general
disturbance, which could result in
short-term behavioral or physiological
responses (e.g., avoidance, stress,
increased heart rate). Misund (1997)
found that fish ahead of a ship showed
avoidance reactions at ranges of 160 to
489 ft (49 to 149 m). Avoidance
behavior of vessels, vertically or
horizontally in the water column, has
been reported for cod and herring, and
was attributed to vessel noise. While
acoustic sources and icebreaking
associated with the proposed action
may influence the behavior of some fish
species, other fish species may be
equally unresponsive. Overall effects to
fish from the proposed action would be
localized, temporary, and infrequent.
Effects to Physical and Foraging
Habitat—Icebreaking activities include
the physical pushing or moving of ice to
allow vessels to proceed through icecovered waters. Breaking of pack ice
that contains hauled out seals may
result in the animals becoming startled
and entering the water, but such effects
would be brief. Bearded and ringed
seals haul out on pack ice during the
spring and summer to molt (Reeves et
al. 2002; Born et al., 2002). Due to the
time of year of the icebreaking activity
(August through October), ringed seals
are not expected to be within the
subnivean lairs nor pupping (Chapskii
1940; McLaren 1958; Smith and Stirling
1975). Additionally, studies by Alliston
(Alliston 1980; Alliston 1981) suggested
that ringed seals may preferentially
establish breathing holes in ship tracks
after icebreakers move through the area.
The amount of ice habitat disturbed by
icebreaking activities is small relative to
the amount of overall habitat available.
There will be no permanent loss or
modification of physical ice habitat
used by bearded or ringed seals.
Icebreaking would have no effect on
physical beluga habitat as beluga habitat
is solely within the water column.
Testing of towed sources and
icebreaking noise would be limited in
duration and the deployed sources that
would remain in use after the vessels
have left the survey area have low duty
cycles and lower source levels. There
would not be any expected habitatrelated effects from non-impulsive
acoustic sources or icebreaking noise
that could impact the in-water habitat of
ringed seal, bearded seal, or beluga
whale foraging habitat.
Estimated Take
This section provides an estimate of
the number of incidental takes proposed
for authorization through this IHA,
which will inform both NMFS’
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consideration of ‘‘small numbers’’ and
the negligible impact determination.
Harassment is the only type of take
expected to result from these activities.
For this military readiness activity, the
MMPA defines ‘‘harassment’’ as (i) Any
act that injures or has the significant
potential to injure a marine mammal or
marine mammal stock in the wild (Level
A harassment); or (ii) Any act that
disturbs or is likely to disturb a marine
mammal or marine mammal stock in the
wild by causing disruption of natural
behavioral patterns, including, but not
limited to, migration, surfacing, nursing,
breeding, feeding, or sheltering, to a
point where such behavioral patterns
are abandoned or significantly altered
(Level B harassment).
Authorized takes would be by Level B
harassment only, in the form of
disruption of behavioral patterns and
TTS for individual marine mammals
resulting from exposure to acoustic
transmissions and icebreaking noise.
Based on the nature of the activity,
Level A harassment is neither
anticipated nor proposed to be
authorized.
As described previously, no mortality
is anticipated or proposed to be
authorized for this activity. Below we
describe how the take is estimated.
Generally speaking, we estimate take
by considering: (1) Acoustic thresholds
above which NMFS believes the best
available science indicates marine
mammals will be behaviorally harassed
or incur some degree of permanent
hearing impairment; (2) the area or
volume of water that will be ensonified
above these levels in a day; (3) the
density or occurrence of marine
mammals within these ensonified areas;
and, (4) and the number of days of
activities. We note that while these
basic factors can contribute to a basic
calculation to provide an initial
prediction of takes, additional
information that can qualitatively
inform take estimates is also sometimes
available (e.g., previous monitoring
results or average group size). For the
proposed IHA, ONR employed a
sophisticated model known as the Navy
Acoustic Effects Model (NAEMO) for
assessing the impacts of underwater
sound. Below, we describe the factors
considered here in more detail and
present the proposed take estimate.
Acoustic Thresholds
Using the best available science,
NMFS has developed acoustic
thresholds that identify the received
level of underwater sound above which
exposed marine mammals would be
reasonably expected to be behaviorally
harassed (equated to Level B
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harassment) or to incur PTS of some
degree (equated to Level A harassment).
Level B Harassment for non-explosive
sources—In coordination with NMFS,
the Navy developed behavioral
thresholds to support environmental
analyses for the Navy’s testing and
training military readiness activities
utilizing active sonar sources; these
behavioral harassment thresholds are
used here to evaluate the potential
effects of the active sonar components of
the proposed action. The response of a
marine mammal to an anthropogenic
sound will depend on the frequency,
duration, temporal pattern and
amplitude of the sound as well as the
animal’s prior experience with the
sound and the context in which the
sound is encountered (i.e., what the
animal is doing at the time of the
exposure). The distance from the sound
source and whether it is perceived as
approaching or moving away can also
affect the way an animal responds to a
sound (Wartzok et al. 2003). For marine
mammals, a review of responses to
anthropogenic sound was first
conducted by Richardson et al. (1995).
Reviews by Nowacek et al. (2007) and
Southall et al. (2007) address studies
conducted since 1995 and focus on
observations where the received sound
level of the exposed marine mammal(s)
was known or could be estimated.
Multi-year research efforts have
conducted sonar exposure studies for
odontocetes and mysticetes (Miller et al.
2012; Sivle et al. 2012). Several studies
with captive animals have provided
data under controlled circumstances for
odontocetes and pinnipeds (Houser et
al. 2013a; Houser et al. 2013b). Moretti
et al. (2014) published a beaked whale
dose-response curve based on passive
acoustic monitoring of beaked whales
during U.S. Navy training activity at
Atlantic Underwater Test and
Evaluation Center during actual AntiSubmarine Warfare exercises. This new
information necessitated the update of
the behavioral response criteria for the
U.S. Navy’s environmental analyses.
Southall et al. (2007), and more
recently Southall et al. (2019),
synthesized data from many past
behavioral studies and observations to
determine the likelihood of behavioral
reactions at specific sound levels. While
in general, the louder the sound source
the more intense the behavioral
response, it was clear that the proximity
of a sound source and the animal’s
experience, motivation, and
conditioning were also critical factors
influencing the response (Southall et al.
2007; Southall et al. 2019). After
examining all of the available data, the
authors felt that the derivation of
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thresholds for behavioral response
based solely on exposure level was not
supported because context of the animal
at the time of sound exposure was an
important factor in estimating response.
Nonetheless, in some conditions,
consistent avoidance reactions were
noted at higher sound levels depending
on the marine mammal species or group
allowing conclusions to be drawn.
Phocid seals showed avoidance
reactions at or below 190 dB re 1 mPa
at 1m; thus, seals may actually receive
levels adequate to produce TTS before
avoiding the source.
Odontocete behavioral criteria for
non-impulsive sources were updated
based on controlled exposure studies for
dolphins and sea mammals, sonar, and
safety (3S) studies where odontocete
behavioral responses were reported after
exposure to sonar (Antunes et al., 2014;
Houser et al., 2013b); Miller et al., 2011;
Miller et al., 2014; Miller et al., 2012).
For the 3S study the sonar outputs
included 1–2 kHz up- and down-sweeps
and 6–7 kHz up-sweeps; source levels
were ramped up from 152–158 dB re 1
mPa to a maximum of 198–214 re 1 mPa
at 1 m. Sonar signals were ramped up
over several pings while the vessel
approached the mammals. The study
did include some control passes of ships
with the sonar off to discern the
behavioral responses of the mammals to
vessel presence alone versus active
sonar.
The controlled exposure studies
included exposing the Navy’s trained
bottlenose dolphins to mid-frequency
sonar while they were in a pen. Midfrequency sonar was played at 6
different exposure levels from 125–185
dB re 1 mPa (rms). The behavioral
response function for odontocetes
resulting from the studies described
above has a 50 percent probability of
response at 157 dB re 1 mPa.
Additionally, distance cutoffs (20 km for
MF cetaceans) were applied to exclude
exposures beyond which the potential
of significant behavioral responses is
considered to be unlikely.
The pinniped behavioral threshold
was updated based on controlled
exposure experiments on the following
captive animals: Hooded seal, gray seal,
and California sea lion (Go¨tz et al. 2010;
Houser et al. 2013a; Kvadsheim et al.
2010). Hooded seals were exposed to
increasing levels of sonar until an
avoidance response was observed, while
the grey seals were exposed first to a
single received level multiple times,
then an increasing received level. Each
individual California sea lion was
exposed to the same received level ten
times. These exposure sessions were
combined into a single response value,
with an overall response assumed if an
animal responded in any single session.
The resulting behavioral response
function for pinnipeds has a 50 percent
probability of response at 166 dB re 1
mPa. Additionally, distance cutoffs (10
km for pinnipeds) were applied to
exclude exposures beyond which the
potential of significant behavioral
responses is considered to be unlikely.
NMFS is proposing to adopt the
Navy’s approach to estimating
incidental take by Level B harassment
from the active acoustic sources for this
action, which includes use of these dose
response functions. The Navy’s dose
response functions were developed to
estimate take from sonar and similar
transducers and are not applicable to
icebreaking. NMFS predicts that marine
mammals are likely to be behaviorally
harassed in a manner we consider Level
B harassment when exposed to
underwater anthropogenic noise above
received levels of 120 dB re 1 mPa (rms)
for continuous (e.g., vibratory piledriving, drilling, icebreaking) and above
160 dB re 1 mPa (rms) for non-explosive
impulsive (e.g., seismic airguns) or
intermittent (e.g., scientific sonar)
sources. Thus, take of marine mammals
by Level B harassment due to
icebreaking has been calculated using
the Navy’s NAEMO model with a stepfunction at 120 dB re 1 mPa (rms)
received level for behavioral response.
Level A harassment for non-explosive
sources—NMFS’ Technical Guidance
for Assessing the Effects of
Anthropogenic Sound on Marine
Mammal Hearing (Version 2.0)
(Technical Guidance, 2018) identifies
dual criteria to assess auditory injury
(Level A harassment) to five different
marine mammal groups (based on
hearing sensitivity) as a result of
exposure to noise from two different
types of sources (impulsive or nonimpulsive). ONR’s proposed activities
involve only non-impulsive sources.
These thresholds are provided in the
table below. The references, analysis,
and methodology used in the
development of the thresholds are
described in NMFS 2018 Technical
Guidance, which may be accessed at
https://www.fisheries.noaa.gov/
national/marine-mammal-protection/
marine-mammal-acoustic-technicalguidance.
TABLE 5—THRESHOLDS IDENTIFYING THE ONSET OF PERMANENT THRESHOLD SHIFT
PTS onset acoustic thresholds *
(received level)
Hearing Group
Impulsive
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Low-Frequency (LF) Cetaceans ......................................
Mid-Frequency (MF) Cetaceans ......................................
High-Frequency (HF) Cetaceans .....................................
Phocid Pinnipeds (PW) ....................................................
(Underwater) ....................................................................
Otariid Pinnipeds (OW) ....................................................
(Underwater) ....................................................................
Cell
Cell
Cell
Cell
1:
3:
5:
7:
Lpk,flat:
Lpk,flat:
Lpk,flat:
Lpk,flat:
219
230
202
218
dB:
dB;
dB;
dB;
Non-impulsive
LE,LF,24h: 183 dB .........................
LE,MF,24h: 185 dB ........................
LE,HF,24h: 155 dB ........................
LE,PW,24h: 185 dB. ......................
Cell 9: Lpk,flat: 232 dB; LE,OW,24h: 203 dB. ......................
Cell
Cell
Cell
Cell
2: LE,LF,24h: 199 dB.
4: LE,MF,24h: 198 dB.
6 LE,HF,24h: 173 dB.
8: LE,PW,24h: 201 dB.
Cell 10: LE,OW,24h: 219 dB.
* Dual metric acoustic thresholds for impulsive sounds: Use whichever results in the largest isopleth for calculating PTS onset. If a non-impulsive sound has the potential of exceeding the peak sound pressure level thresholds associated with impulsive sounds, these thresholds should
also be considered.
Note:—Peak sound pressure (Lpk) has a reference value of 1 μPa, and cumulative sound exposure level (LE) has a reference value of 1μPa2s.
In this Table, thresholds are abbreviated to reflect American National Standards Institute standards (ANSI 2013). However, peak sound pressure
is defined by ANSI as incorporating frequency weighting, which is not the intent for this Technical Guidance. Hence, the subscript ‘‘flat’’ is being
included to indicate peak sound pressure should be flat weighted or unweighted within the generalized hearing range. The subscript associated
with cumulative sound exposure level thresholds indicates the designated marine mammal auditory weighting function (LF, MF, and HF
cetaceans, and PW and OW pinnipeds) and that the recommended accumulation period is 24 hours. The cumulative sound exposure level
thresholds could be exceeded in a multitude of ways (i.e., varying exposure levels and durations, duty cycle). When possible, it is valuable for
action proponents to indicate the conditions under which these acoustic thresholds will be exceeded.
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Quantitative Modeling
The Navy performed a quantitative
analysis to estimate the number of
mammals that could be harassed by the
underwater acoustic transmissions
during the proposed action. Inputs to
the quantitative analysis included
marine mammal density estimates,
marine mammal depth occurrence
distributions (Navy 2017a),
oceanographic and environmental data,
marine mammal hearing data, and
criteria and thresholds for levels of
potential effects. The quantitative
analysis consists of computer modeled
estimates and a post-model analysis to
determine the number of potential
animal exposures. The model calculates
sound energy propagation from the
proposed non-impulsive acoustic
sources and icebreaking, the sound
received by animat (virtual animal)
dosimeters representing marine
mammals distributed in the area around
the modeled activity, and whether the
sound received by animats exceeds the
thresholds for effects.
The Navy developed a set of software
tools and compiled data for estimating
acoustic effects on marine mammals
without consideration of behavioral
avoidance or mitigation. These tools and
data sets serve as integral components of
NAEMO. In NAEMO, animats are
distributed non-uniformly based on
species-specific density, depth
distribution, and group size information
and animats record energy received at
their location in the water column. A
fully three-dimensional environment is
used for calculating sound propagation
and animat exposure in NAEMO. Sitespecific bathymetry, sound speed
profiles, wind speed, and bottom
properties are incorporated into the
propagation modeling process. NAEMO
calculates the likely propagation for
various levels of energy (sound or
pressure) resulting from each source
used during the training event.
NAEMO then records the energy
received by each animat within the
energy footprint of the event and
calculates the number of animats having
received levels of energy exposures that
fall within defined impact thresholds.
Predicted effects on the animats within
a scenario are then tallied and the
highest order effect (based on severity of
criteria; e.g., PTS over TTS) predicted
for a given animat is assumed. Each
scenario, or each 24-hour period for
scenarios lasting greater than 24 hours
(which NMFS recommends in order to
ensure more consistent quantification of
take across actions), is independent of
all others, and therefore, the same
individual marine animal (as
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represented by an animat in the model
environment) could be impacted during
each independent scenario or 24-hour
period. In few instances, although the
activities themselves all occur within
the study area, sound may propagate
beyond the boundary of the study area.
Any exposures occurring outside the
boundary of the study area are counted
as if they occurred within the study area
boundary. NAEMO provides the initial
estimated impacts on marine species
with a static horizontal distribution (i.e.,
animats in the model environment do
not move horizontally).
There are limitations to the data used
in the acoustic effects model, and the
results must be interpreted within this
context. While the best available data
and appropriate input assumptions have
been used in the modeling, when there
is a lack of definitive data to support an
aspect of the modeling, conservative
modeling assumptions have been
chosen (i.e., assumptions that may
result in an overestimate of acoustic
exposures):
• Animats are modeled as being
underwater, stationary, and facing the
source and therefore always predicted to
receive the maximum potential sound
level at a given location (i.e., no
porpoising or pinnipeds’ heads above
water);
• Animats do not move horizontally
(but change their position vertically
within the water column), which may
overestimate physiological effects such
as hearing loss, especially for slow
moving or stationary sound sources in
the model;
• Animats are stationary horizontally
and therefore do not avoid the sound
source, unlike in the wild where
animals would most often avoid
exposures at higher sound levels,
especially those exposures that may
result in PTS;
• Multiple exposures within any 24hour period are considered one
continuous exposure for the purposes of
calculating potential threshold shift,
because there are not sufficient data to
estimate a hearing recovery function for
the time between exposures; and
• Mitigation measures were not
considered in the model. In reality,
sound-producing activities would be
reduced, stopped, or delayed if marine
mammals are detected by visual
monitoring.
Because of these inherent model
limitations and simplifications, modelestimated results should be further
analyzed, considering such factors as
the range to specific effects, avoidance,
and the likelihood of successfully
implementing mitigation measures. This
analysis uses a number of factors in
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addition to the acoustic model results to
predict acoustic effects on marine
mammals.
The underwater radiated noise
signature for icebreaking in the central
Arctic Ocean by CGC HEALY during
different types of ice-cover was
characterized in Roth et al. (2013). The
radiated noise signatures were
characterized for various fractions of ice
cover. For modeling, the 8/10 ice cover
was used. Each modeled day of
icebreaking consisted of 6 hours of 8/10
ice cover. Icebreaking was modeled for
eight days for each of the 2019 and 2020
cruises. For each cruise, this includes
four days of icebreaking for the
deployment (or recovery) of the VLF
source and four days of icebreaking for
the deployment (or recovery) of the
northernmost navigation sources. Since
ice forecasting cannot be predicted more
than a few weeks in advance it is
unknown if icebreaking would be
needed to deploy or retrieve the sources
after one year of transmitting. Therefore,
icebreaking was conservatively analyzed
within this IHA. Figure 5a and 5b in
Roth et al. (2013) depicts the source
spectrum level versus frequency for 8/
10 ice cover. The sound signature of the
ice coverage level was broken into 1octave bins (Table 6). In the model, each
bin was included as a separate source
on the modeled vessel. When these
independent sources go active
concurrently, they simulate the sound
signature of CGC HEALY. The modeled
source level summed across these bins
was 196.2 dB for the 8/10 signature ice
signature. These source levels are a good
approximation of the icebreaker’s
observed source level (provided in
Figure 4b of (Roth et al. 2013)). Each
frequency and source level was modeled
as an independent source, and applied
simultaneously to all of the animats
within NAEMO. Each second was
summed across frequency to estimate
sound pressure level (root mean square
(SPLRMS)). For PTS and TTS
determinations, sound exposure levels
were summed over the duration of the
test and the transit to the deployment
area. The method of quantitative
modeling for icebreaking is considered
to be a conservative approach; therefore,
the number of takes estimated for
icebreaking are likely an over-estimate
and would not be expected.
TABLE 6—MODELED BINS FOR
ICEBREAKING IN 8/10 ICE COVERAGE
ON CGC HEALY
Frequency
(Hz)
25 ..............................................
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(dB)
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each active emission during an event.
TABLE 6—MODELED BINS FOR
ICEBREAKING IN 8/10 ICE COVERAGE This is done by taking the following
factors into account over the
ON CGC HEALY—Continued
Frequency
(Hz)
Source level
(dB)
50 ..............................................
100 ............................................
200 ............................................
400 ............................................
800 ............................................
1600 ..........................................
3200 ..........................................
6400 ..........................................
12800 ........................................
188
189
190
188
183
177
176
172
167
For the other non-impulsive sources,
NAEMO calculates the SPL and SEL for
propagation paths: Bathymetric relief
and bottom types, sound speed, and
attenuation contributors such as
absorption, bottom loss, and surface
loss. Platforms such as a ship using one
or more sound sources are modeled in
accordance with relevant vehicle
dynamics and time durations by moving
them across an area whose size is
representative of the testing event’s
operational area. Table 7 provides range
to effects for non-impulsive sources and
icebreaking noise proposed for the
Arctic research activities to midfrequency cetacean and pinniped
specific criteria. Marine mammals
within these ranges would be predicted
to receive the associated effect. Range to
effects is important information in not
only predicting non-impulsive acoustic
impacts, but also in verifying the
accuracy of model results against realworld situations and determining
adequate mitigation ranges to avoid
higher level effects, especially
physiological effects in marine
mammals. Therefore, the ranges in
Table 7 provide realistic maximum
distances over which the specific effects
from the use of non-impulsive sources
during the proposed action would be
possible.
TABLE 7—RANGE TO PTS, TTS, AND BEHAVIORAL EFFECTS IN THE STUDY AREA
Range to behavioral effects
(m)
Range to TTS effects
(m)
Range to PTS effects
(m)
Source
Piniped
cetacean
MF
20,000 a
20,000 a
4,275
Navigation and real-time sensing sources
Spiral Wave Beacon source ....................
Icebreaking noise .....................................
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a Cutoff
Piniped
cetacean
MF
10,000 a
10,000 a
4,525
0
0
3
Piniped
cetacean
MF
6
0
12
0
0
0
0
0
0
distances applied.
A behavioral response study
conducted on and around the Navy
range in Southern California (SOCAL
BRS) observed reactions to sonar and
similar sound sources by several marine
mammal species, including Risso’s
dolphins (Grampus griseus), a midfrequency cetacean (DeRuiter et al.,
2013; Goldbogen et al., 2013; Southall et
al., 2011; Southall et al., 2012; Southall
et al., 2013; Southall et al., 2014). In
preliminary analysis, none of the Risso’s
dolphins exposed to simulated or real
mid-frequency sonar demonstrated any
overt or obvious responses (Southall et
al., 2012, Southall et al., 2013). In
general, although the responses to the
simulated sonar were varied across
individuals and species, none of the
animals exposed to real Navy sonar
responded; these exposures occurred at
distances beyond 10 km, and were up to
100 km away (DeRuiter et al., 2013; B.
Southall pers. comm.). These data
suggest that most odontocetes (not
including beaked whales and harbor
porpoises) likely do not exhibit
significant behavioral reactions to sonar
and other transducers beyond
approximately 10 km. Therefore, the
Navy uses a cutoff distance for
odontocetes of 10 km for moderate
source level, single platform training
and testing events, and 20 km for all
other events, including the proposed
Arctic Research Activities (Navy 2017a).
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Southall et al., (2007) report that
pinnipeds do not exhibit strong
reactions to SPLs up to 140 dB re 1 mPa
from non-impulsive sources. While
there are limited data on pinniped
behavioral responses beyond about 3 km
in the water, the Navy uses a distance
cutoff of 5 km for moderate source level,
single platform training and testing
events, and 10 km for all other events,
including the proposed Arctic Research
Activities (Navy 2017a).
NMFS and the Navy conservatively
propose a distance cutoff of 10 km for
pinnipeds, and 20 km for mid-frequency
cetaceans (Navy 2017a). Regardless of
the received level at that distance, take
is not estimated to occur beyond 10 and
20 km from the source for pinnipeds
and cetaceans, respectively. Sources
that show a range of zero do not rise to
the specified level of effects (i.e., there
is no chance of PTS for either MF
cetaceans or pinnipeds from any of the
sources). No instances of PTS were
modeled for any species or stock; as
such, no take by Level A harassment is
anticipated or proposed to be
authorized.
As discussed above, within NAEMO
animats do not move horizontally or
react in any way to avoid sound.
Furthermore, mitigation measures that
reduce the likelihood of physiological
impacts are not considered in
quantitative analysis. Therefore, the
model may overestimate acoustic
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impacts, especially physiological
impacts near the sound source. The
behavioral criteria used as a part of this
analysis acknowledges that a behavioral
reaction is likely to occur at levels
below those required to cause hearing
loss. At close ranges and high sound
levels approaching those that could
cause PTS, avoidance of the area
immediately around the sound source is
the assumed behavioral response for
most cases.
In previous environmental analyses,
the Navy has implemented analytical
factors to account for avoidance
behavior and the implementation of
mitigation measures. The application of
avoidance and mitigation factors has
only been applied to model-estimated
PTS exposures given the short distance
over which PTS is estimated. Given that
no PTS exposures were estimated
during the modeling process for this
proposed action, the quantitative
consideration of avoidance and
mitigation factors were not included in
this analysis.
The marine mammal density numbers
utilized for quantitative modeling are
from the Navy Marine Species Density
Database (Navy 2014). Density estimates
are based on habitat-based modeling by
Kaschner et al., (2006) and Kaschner
(2004). While density estimates for the
two stocks of beluga whales are equal
(Kaschner et al., 2006; Kaschner 2004),
take has been apportioned to each stock
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proportional to the abundance of each
stock. Table 8 shows the exposures
expected for the beluga whale, bearded
seal, and ringed seal based on NAEMO
modeled results.
TABLE 8—QUANTITATIVE MODELING RESULTS OF POTENTIAL EXPOSURES
Density
estimate
within
study area
(animals per
square km) a
Species
Beluga Whale (Beaufort Sea Stock) ........
Beluga Whale (Eastern Chukchi Sea
stock) ....................................................
Bearded Seal ...........................................
Ringed Seal .............................................
Level B
harassment
from deployed
sources
Level B
harassment
from
icebreaking
Total
proposed
take
Level A
harassment
Percentage of
stock
taken
0.0087
331
32
0
363
0.92
0.0087
0.0332
0.3760
178
0
6,773
18
0
1,072
0
0
0
196
b5
7,845
0.94
<0.01
2.17
a Kaschner
et al. (2006); Kaschner (2004)
modeling yielded zero takes of bearded seals. However, in an abundance of caution, we are proposing to authorize five takes of
bearded seals by Level B harassment.
b Quantitative
Effects of Specified Activities on
Subsistence Uses of Marine Mammals
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Subsistence hunting is important for
many Alaska Native communities. A
study of the North Slope villages of
Nuiqsut, Kaktovik, and Barrow
identified the primary resources used
for subsistence and the locations for
harvest (Stephen R. Braund & Associates
2010), including terrestrial mammals
(caribou, moose, wolf, and wolverine),
birds (geese and eider), fish (Arctic
cisco, Arctic char/Dolly Varden trout,
and broad whitefish), and marine
mammals (bowhead whale, ringed seal,
bearded seal, and walrus). Bearded
seals, ringed seals, and beluga whales
are located within the study area during
the proposed action. The permitted
sources would be placed outside of the
range for subsistence hunting and the
study plans have been communicated to
the Native communities. The closest
active acoustic source within the study
area (aside from the de minimis
sources), is approximately 145 mi (233
km) from land. As stated above, the
range to effects for non-impulsive
acoustic sources in this experiment is
much smaller than the distance from
shore. In addition, the proposed action
would not remove individuals from the
population. Therefore, there would be
no impacts caused by this action to the
availability of bearded seal, ringed seal,
or beluga whale for subsistence hunting.
Therefore, subsistence uses of marine
mammals are not expected to be
impacted by the proposed action.
Proposed Mitigation
In order to issue an IHA 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
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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. NMFS
regulations require applicants for
incidental take authorizations to include
information about the availability and
feasibility (economic and technological)
of equipment, methods, and manner of
conducting such activity or other means
of effecting the least practicable adverse
impact upon the affected species or
stocks and their habitat (50 CFR
216.104(a)(11)). The NDAA for FY 2004
amended the MMPA as it relates to
military readiness activities and the
incidental take authorization process
such that ‘‘least practicable impact’’
shall include consideration of personnel
safety, practicality of implementation,
and impact on the effectiveness of the
military readiness activity.
In evaluating how mitigation may or
may not be appropriate to ensure the
least practicable adverse impact on
species or stocks and their habitat, as
well as subsistence uses where
applicable, we carefully consider two
primary factors:
(1) The manner in which, and the
degree to which, the successful
implementation of the measure(s) is
expected to reduce impacts to marine
mammals, marine mammal species or
stocks, and their habitat, as well as
subsistence uses. This considers the
nature of the potential adverse impact
being mitigated (likelihood, scope,
range). It further considers the
likelihood that the measure will be
effective if implemented (probability of
accomplishing the mitigating result if
implemented as planned), the
likelihood of effective implementation
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(probability implemented as planned),
and;
(2) The practicability of the measures
for applicant implementation, which
may consider such things as cost,
impact on operations, and, in the case
of a military readiness activity,
personnel safety, practicality of
implementation, and impact on the
effectiveness of the military readiness
activity.
Mitigation for Marine Mammals and
Their Habitat
Ships operated by or for the Navy
have personnel assigned to stand watch
at all times, day and night, when
moving through the water. While in
transit, ships must use extreme caution
and proceed at a safe speed such that
the ship can take proper and effective
action to avoid a collision with any
marine mammal and can be stopped
within a distance appropriate to the
prevailing circumstances and
conditions.
During navigational source
deployments, visual observation would
start 30 minutes prior to and continue
throughout the deployment within an
exclusion zone of 55 m (180 ft, roughly
one ship length) around the deployed
mooring. Deployment will stop if a
marine mammal is visually detected
within the exclusion zone. Deployment
will re-commence if any one of the
following conditions are met: (1) The
animal is observed exiting the exclusion
zone, (2) the animal is thought to have
exited the exclusion zone based on its
course and speed, or (3) the exclusion
zone has been clear from any additional
sightings for a period of 15 minutes for
pinnipeds and 30 minutes for cetaceans.
Visual monitoring will continue through
30 minutes following the deployment of
sources.
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Once deployed, the spiral wave
beacon would transmit for five days.
The ship will maintain position near the
moored source and will monitor the
surrounding area for marine mammals.
Transmission will cease if a marine
mammal enters a 55-m (180 ft)
exclusion zone. Transmission will recommence if any one of the following
conditions are met: (1) The animal is
observed exiting the exclusion zone, (2)
the animal is thought to have exited the
exclusion zone based on its course and
speed and relative motion between the
animal and the source, or (3) the
exclusion zone has been clear from any
additional sightings for a period of 15
minutes for pinnipeds and 30 minutes
for cetaceans. The spiral wave beacon
source will only transmit during
daylight hours.
Ships would avoid approaching
marine mammals head on and would
maneuver to maintain an exclusion zone
of 1,500 ft (457 m) around observed
mysticete whales, and 600 ft (183 m)
around all other marine mammals,
provided it is safe to do so in ice free
waters.
With the exception of the spiral wave
beacon, moored/drifting sources are left
in place and cannot be turned off until
the following year during ice free
months. Once they are programmed
they will operate at the specified pulse
lengths and duty cycles until they are
either turned off the following year or
there is failure of the battery and are not
able to operate. Due to the ice covered
nature of the Arctic is in not possible to
recover the sources or interfere with
their transmit operations in the middle
of the deployment.
These requirements do not apply if a
vessel’s safety is at risk, such as when
a change of course would create an
imminent and serious threat to safety,
person, vessel, or aircraft, and to the
extent vessels are restricted in their
ability to maneuver. No further action is
necessary if a marine mammal other
than a whale continues to approach the
vessel after there has already been one
maneuver and/or speed change to avoid
the animal. Avoidance measures should
continue for any observed whale in
order to maintain an exclusion zone of
1,500 ft (457 m).
All personnel conducting on-ice
experiments, as well as all aircraft
operating in the study area, are required
to maintain a separation distance of
1,000 ft (305 m) from any sighted
marine mammal.
Based on our evaluation of the
applicant’s proposed measures, NMFS
has preliminarily determined that the
proposed mitigation measures provide
the means effecting the least practicable
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impact on the affected species or stocks
and their habitat, paying particular
attention to rookeries, mating grounds,
areas of similar significance, and on the
availability of such species or stock for
subsistence uses.
Proposed Monitoring and Reporting
In order to issue an IHA 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 authorizations 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.
Effective reporting is critical both to
compliance as well as ensuring that the
most value is obtained from the required
monitoring.
Monitoring and reporting
requirements prescribed by NMFS
should contribute to improved
understanding of one or more of the
following:
• Occurrence of marine mammal
species or stocks in the area in which
take is anticipated (e.g., presence,
abundance, distribution, density);
• Nature, scope, or context of likely
marine mammal exposure to potential
stressors/impacts (individual or
cumulative, acute or chronic), through
better understanding of: (1) Action or
environment (e.g., source
characterization, propagation, ambient
noise); (2) affected species (e.g., life
history, dive patterns); (3) co-occurrence
of marine mammal species with the
action; or (4) biological or behavioral
context of exposure (e.g., age, calving or
feeding areas);
• Individual marine mammal
responses (behavioral or physiological)
to acoustic stressors (acute, chronic, or
cumulative), other stressors, or
cumulative impacts from multiple
stressors;
• How anticipated responses to
stressors impact either: (1) Long-term
fitness and survival of individual
marine mammals; or (2) populations,
species, or stocks;
• Effects on marine mammal habitat
(e.g., marine mammal prey species,
acoustic habitat, or other important
physical components of marine
mammal habitat); and
• Mitigation and monitoring
effectiveness.
While underway, the ships (including
non-Navy ships operating on behalf of
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the Navy) utilizing active acoustics will
have at least one watch person during
activities. Watch personnel undertake
extensive training in accordance with
the U.S. Navy Lookout Training
Handbook or civilian equivalent,
including on the job instruction and a
formal Personal Qualification Standard
program (or equivalent program for
supporting contractors or civilians), to
certify that they have demonstrated all
necessary skills (such as detection and
reporting of floating or partially
submerged objects). Additionally, watch
personnel have taken the Navy’s Marine
Species Awareness Training. Their
duties may be performed in conjunction
with other job responsibilities, such as
navigating the ship or supervising other
personnel. While on watch, personnel
employ visual search techniques,
including the use of binoculars, using a
scanning method in accordance with the
U.S. Navy Lookout Training Handbook
or civilian equivalent. A primary duty of
watch personnel is to detect and report
all objects and disturbances sighted in
the water that may be indicative of a
threat to the ship and its crew, such as
debris, or surface disturbance. Per safety
requirements, watch personnel also
report any marine mammals sighted that
have the potential to be in the direct
path of the ship as a standard collision
avoidance procedure.
The U.S. Navy has coordinated with
NMFS to develop an overarching
program plan in which specific
monitoring would occur. This plan is
called the Integrated Comprehensive
Monitoring Program (ICMP) (Navy
2011). The ICMP has been developed in
direct response to Navy permitting
requirements established through
various environmental compliance
efforts. As a framework document, the
ICMP applies by regulation to those
activities on ranges and operating areas
for which the Navy is seeking or has
sought incidental take authorizations.
The ICMP is intended to coordinate
monitoring efforts across all regions and
to allocate the most appropriate level
and type of effort based on a set of
standardized research goals, and in
acknowledgement of regional scientific
value and resource availability.
The ICMP is focused on Navy training
and testing ranges where the majority of
Navy activities occur regularly as those
areas have the greatest potential for
being impacted. ONR’s Arctic Research
Activities in comparison is a less
intensive test with little human activity
present in the Arctic. Human presence
is limited to a minimal amount of days
for source operations and source
deployments, in contrast to the large
majority (>95%) of time that the sources
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will be left behind and operate
autonomously. Therefore, a dedicated
monitoring project is not warranted.
However, ONR will record all
observations of marine mammals,
including the marine mammal’s location
(latitude and longitude), behavior, and
distance from project activities,
including icebreaking.
The Navy is committed to
documenting and reporting relevant
aspects of research and testing activities
to verify implementation of mitigation,
comply with permits, and improve
future environmental assessments. If
any injury or death of a marine mammal
is observed during the 2019–20 Arctic
Research Activities, the Navy will
immediately halt the activity and report
the incident to the Office of Protected
Resources, NMFS, and the Alaska
Regional Stranding Coordinator, NMFS.
The following information must be
provided:
• Time, date, and location of the
discovery;
• Species identification (if known) or
description of the animal(s) involved;
• Condition of the animal(s)
(including carcass condition if the
animal is dead);
• Observed behaviors of the
animal(s), if alive;
• If available, photographs or video
footage of the animal(s); and
• General circumstances under which
the animal(s) was discovered (e.g.,
during use of towed acoustic sources,
deployment of moored or drifting
sources, during on-ice experiments, or
by transiting vessel).
ONR will provide NMFS with a draft
exercise monitoring report within 90
days of the conclusion of the proposed
activity. The draft exercise monitoring
report will include data regarding
acoustic source use and any mammal
sightings or detection will be
documented. The report will include
the estimated number of marine
mammals taken during the activity. The
report will also include information on
the number of shutdowns recorded. If
no comments are received from NMFS
within 30 days of submission of the
draft final report, the draft final report
will constitute the final report. If
comments are received, a final report
must be submitted within 30 days after
receipt of comments.
Negligible Impact Analysis and
Determination
NMFS has defined negligible impact
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
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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 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 harassment, NMFS considers
other factors, such as the likely nature
of any responses (e.g., intensity,
duration), the context of any responses
(e.g., critical reproductive time or
location, migration), as well as effects
on habitat, and the likely effectiveness
of the mitigation. We also assess the
number, intensity, and context of
estimated takes by evaluating this
information relative to population
status. Consistent with the 1989
preamble for NMFS’s implementing
regulations (54 FR 40338; September 29,
1989), the impacts from other past and
ongoing anthropogenic activities are
incorporated into this analysis via their
impacts on the environmental baseline
(e.g., as reflected in the regulatory status
of the species, population size and
growth rate where known, ongoing
sources of human-caused mortality, or
ambient noise levels).
Underwater acoustic transmissions
associated with the Arctic Research
Activities, as outlined previously, have
the potential to result in Level B
harassment of beluga whales, ringed
seals, and bearded seals in the form of
TTS and behavioral disturbance. No
serious injury, mortality, or Level A
harassment are anticipated to result
from this activity.
Minimal takes of marine mammals by
Level B harassment would be due to
TTS since the range to TTS effects is
small at only 12 m or less while the
behavioral effects range is significantly
larger extending up to 20 km (Table 7).
TTS is a temporary impairment of
hearing and can last from minutes or
hours to days (in cases of strong TTS).
In many cases, however, hearing
sensitivity recovers rapidly after
exposure to the sound ends. No takes
from TTS were modeled, but if TTS did
occur, the overall fitness of the
individual is unlikely to be affected and
negative impacts to the relevant stock
are not anticipated.
Effects on individuals that are taken
by Level B harassment could include
alteration of dive behavior, alteration of
foraging behavior, effects to breathing
rates, interference with or alteration of
vocalization, avoidance, and flight.
More severe behavioral responses are
not anticipated due to the localized,
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37261
intermittent use of active acoustic
sources. Most likely, individuals will
simply be temporarily displaced by
moving away from the sound source. As
described previously in the behavioral
effects section, seals exposed to nonimpulsive sources with a received
sound pressure level within the range of
calculated exposures (142–193 dB re 1
mPa), have been shown to change their
behavior by modifying diving activity
and avoidance of the sound source (Go¨tz
et al., 2010; Kvadsheim et al., 2010).
Although a minor change to a behavior
may occur as a result of exposure to the
sound sources associated with the
proposed action, these changes would
be within the normal range of behaviors
for the animal (e.g., the use of a
breathing hole further from the source,
rather than one closer to the source,
would be within the normal range of
behavior). Thus, even repeated Level B
harassment of some small subset of the
overall stock is unlikely to result in any
significant realized decrease in fitness
for the affected individuals, and would
not result in any adverse impact to the
stock as a whole.
The project is not expected to have
significant adverse effects on marine
mammal habitat. While the activities
may cause some fish to leave the area
of disturbance, temporarily impacting
marine mammals’ foraging
opportunities, this would encompass a
relatively small area of habitat leaving
large areas of existing fish and marine
mammal foraging habitat unaffected.
Icebreaking may temporarily affect the
availability of pack ice for seals to haul
out but the proportion of ice disturbed
is small relative to the overall amount
of available ice habitat. Icebreaking will
not occur during the time of year when
ringed seals are expected to be within
subnivean lairs or pupping (Chapskii
1940; McLaren 1958; Smith and Stirling
1975). As such, the impacts to marine
mammal habitat are not expected to
cause significant or long-term negative
consequences.
In summary and as described above,
the following factors primarily support
our preliminary determination that the
impacts resulting from this activity are
not expected to adversely affect the
species or stock through effects on
annual rates of recruitment or survival:
• No mortality is anticipated or
authorized;
• Impacts will be limited to Level B
harassment;
• Takes by Level B harassment will
primarily be in the form of behavioral
disturbance; and
• There will be no permanent or
significant loss or modification of
marine mammal prey or habitat.
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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
the proposed activity will have a
negligible impact on all affected marine
mammal species or stocks.
Unmitigable Adverse Impact Analysis
and Determination
Impacts to subsistence uses of marine
mammals resulting from the proposed
action are not anticipated. The closest
active acoustic source within the study
area is approximately 145 mi (233 km)
from land, outside of known subsistence
use areas. Based on this information,
NMFS has preliminarily determined
that there will be no unmitigable
adverse impact on subsistence uses from
ONR’s proposed activities.
Endangered Species Act (ESA)
Section 7(a)(2) of the Endangered
Species Act of 1973 (16 U.S.C. 1531 et
seq.) requires that each Federal agency
insure that any action it authorizes,
funds, or carries out is not likely to
jeopardize the continued existence of
any endangered or threatened species or
result in the destruction or adverse
modification of designated critical
habitat. To ensure ESA compliance for
the issuance of IHAs, NMFS consults
internally, in this case with the NMFS
Alaska Regional Office (AKR), whenever
we propose to authorize take for
endangered or threatened species.
NMFS is proposing to authorize take
of ringed seals and bearded seals, which
are listed under the ESA. The Permits
and Conservation Division has
requested initiation of section 7
consultation with the Protected
Resources Division of AKR for the
issuance of this IHA. NMFS will
conclude the ESA consultation prior to
reaching a determination regarding the
proposed issuance of the authorization.
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Proposed Authorization
As a result of these preliminary
determinations, NMFS proposes to issue
an IHA to ONR for conducting Arctic
Research Activities in the Beaufort and
Chukchi Seas, provided the previously
mentioned mitigation, monitoring, and
reporting requirements are incorporated.
A draft of the proposed IHA can be
found at https://
www.fisheries.noaa.gov/permit/
incidental-take-authorizations-undermarine-mammal-protection-act.
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Request for Public Comments
We request comment on our analyses,
the proposed authorization, and any
other aspect of this Notice of Proposed
IHA for the proposed action. We also
request at this time comment on the
potential renewal of this proposed IHA
as described in the paragraph below.
Please include with your comments any
supporting data or literature citations to
help inform decisions on the request for
this IHA or a subsequent Renewal.
On a case-by-case basis, NMFS may
issue a one-year IHA renewal with an
additional 15 days for public comments
when (1) another year of identical or
nearly identical activities as described
in the Specified Activities section of
this notice is planned or (2) the
activities as described in the Specified
Activities section of this notice would
not be completed by the time the IHA
expires and a second IHA would allow
for completion of the activities beyond
that described in the Dates and Duration
section of this notice, provided all of the
following conditions are met:
• A request for renewal is received no
later than 60 days prior to expiration of
the current IHA;
• The request for renewal must
include the following:
(1) An explanation that the activities
to be conducted under the requested
Renewal are identical to the activities
analyzed under the initial IHA, are a
subset of the activities, or include
changes so minor (e.g., reduction in pile
size) that the changes do not affect the
previous analyses, mitigation and
monitoring requirements, or take
estimates (with the exception of
reducing the type or amount of take
because only a subset of the initially
analyzed activities remain to be
completed under the Renewal); and
(2) A preliminary monitoring report
showing the results of the required
monitoring to date and an explanation
showing that the monitoring results do
not indicate impacts of a scale or nature
not previously analyzed or authorized.
• Upon review of the request for
Renewal, the status of the affected
species or stocks, and any other
pertinent information, NMFS
determines that there are no more than
minor changes in the activities, the
mitigation and monitoring measures
will remain the same and appropriate,
and the findings in the initial IHA
remain valid.
Dated: July 26, 2019.
Catherine Marzin,
Acting Director, Office of Protected Resources,
National Marine Fisheries Service.
[FR Doc. 2019–16318 Filed 7–30–19; 8:45 am]
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National Oceanic and Atmospheric
Administration
RIN 0648–XV009
Mid-Atlantic Fishery Management
Council (MAFMC); Public Meetings
National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice; public meeting.
AGENCY:
The Mid-Atlantic Fishery
Management Council’s (Council) Spiny
Dogfish Advisory Panel (AP) will meet
to review recent fishery performance
and develop a Fishery Performance
Report and/or other recommendations
in preparation for review of the annual
specifications that commence May 1,
2020. Potential federal trip limit
modifications will also be discussed.
DATES: The meeting will be held
Monday, August 19, 2019, from 1 p.m.
to 4:30 p.m.
ADDRESSES: The meeting will be held
via webinar, but anyone can also attend
at the Council office address (see
below). The webinar link is: https://
mafmc.adobeconnect.com/dogfishap
2019/. Please call the Council at least 24
hours in advance if you wish to attend
at the Council office.
Council address: Mid-Atlantic Fishery
Management Council, 800 N State St.,
Suite 201, Dover, DE 19901; telephone:
(302) 674–2331.
FOR FURTHER INFORMATION CONTACT:
Christopher M. Moore, Ph.D. Executive
Director, Mid-Atlantic Fishery
Management Council; telephone: (302)
526–5255. The Council’s website,
www.mafmc.org also has details on the
proposed agenda, webinar access, and
briefing materials.
SUPPLEMENTARY INFORMATION: The
purpose of the meeting is to create a
Fishery Performance Report by the
Council’s Spiny Dogfish Advisory
Panel. The report facilitates structured
input from the Advisory Panel members
into the specification’s development
process. Potential federal trip limit
modifications will also be discussed.
SUMMARY:
Special Accommodations
The meeting is physically accessible
to people with disabilities. Requests for
sign language interpretation or other
auxiliary aid should be directed to M.
Jan Saunders, (302) 526–5251, at least 5
days prior to the meeting date.
Authority: 16 U.S.C. 1801 et seq.
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Agencies
[Federal Register Volume 84, Number 147 (Wednesday, July 31, 2019)]
[Notices]
[Pages 37240-37262]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-16318]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
RIN 0648-XR023
Takes of Marine Mammals Incidental to Specified Activities;
Taking Marine Mammals Incidental to Office of Naval Research Arctic
Research Activities
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice; proposed incidental harassment authorization; request
for comments on proposed authorization and possible renewal.
-----------------------------------------------------------------------
SUMMARY: NMFS has received a request from the U.S. Navy's Office of
Naval Research (ONR) for authorization to take marine mammals
incidental to Arctic Research Activities in the Beaufort and Chukchi
Seas. Pursuant to the Marine Mammal Protection Act (MMPA), NMFS is
requesting comments on its proposal to issue an incidental harassment
authorization (IHA) to incidentally take marine mammals during the
specified activities. NMFS is also requesting comments on a possible
one-year renewal that could be issued under certain circumstances and
if all requirements are met, as described in Request for Public
Comments at the end of this notice. NMFS will consider public comments
prior to making any final decision on the issuance of the requested
MMPA authorizations and agency responses will be summarized in the
final notice of our decision. ONR's activities are considered military
readiness activities pursuant to the Marine Mammal Protection Act
(MMPA), as amended by the National Defense Authorization Act for Fiscal
Year 2004 (NDAA).
DATES: Comments and information must be received no later than August
30, 2019.
ADDRESSES: Comments should be addressed to Jolie Harrison, Chief,
Permits and Conservation Division, Office of Protected Resources,
National Marine Fisheries Service. Physical comments should be sent to
1315 East-West Highway, Silver Spring, MD 20910 and electronic comments
should be sent to [email protected].
Instructions: NMFS is not responsible for comments sent by any
other method, to any other address or individual, or received after the
end of the comment period. Comments received electronically, including
all attachments, must not exceed a 25-megabyte file size. Attachments
to electronic comments will be accepted in Microsoft Word or Excel or
Adobe PDF file formats only. All comments received are a part of the
public record and will generally be posted online at https://www.fisheries.noaa.gov/permit/incidental-take-authorizations-under-marine-mammal-protection-act 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.
FOR FURTHER INFORMATION CONTACT: Amy Fowler, Office of Protected
Resources, NMFS, (301) 427-8401. Electronic copies of the application
and supporting documents, as well as a list of the references cited in
this document, may be obtained online at: https://www.fisheries.noaa.gov/permit/incidental-take-authorizations-under-marine-mammal-protection-act. In case of problems accessing these
documents, please call the contact listed above.
SUPPLEMENTARY INFORMATION:
Background
The MMPA prohibits the ``take'' of marine mammals, with certain
exceptions. Sections 101(a)(5)(A) and (D) of the MMPA (16 U.S.C. 1361
et seq.) direct the Secretary of Commerce (as delegated to NMFS) 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 incidental take authorization may be provided to the public
for review.
[[Page 37241]]
Authorization for incidental takings shall be granted if NMFS finds
that the taking will have a negligible impact on the species or
stock(s) and will not have an unmitigable adverse impact on the
availability of the species or stock(s) for taking for subsistence uses
(where relevant). Further, NMFS must prescribe the permissible methods
of taking and other ``means of effecting the least practicable adverse
impact'' on the affected species or stocks and their habitat, paying
particular attention to rookeries, mating grounds, and areas of similar
significance, and on the availability of such species or stocks for
taking for certain subsistence uses (referred to in shorthand as
``mitigation''); and requirements pertaining to the mitigation,
monitoring and reporting of such takings are set forth.
The NDAA (Pub. L. 108-136) removed the ``small numbers'' and
``specified geographical region'' limitations indicated above and
amended the definition of ``harassment'' as it applies to a ``military
readiness activity.'' The activity for which incidental take of marine
mammals is being requested addressed here qualifies as a military
readiness activity. The definitions of all applicable MMPA statutory
terms cited above are included in the relevant sections below. The
proposed action constitutes a military readiness activity because these
proposed scientific research activities directly support the adequate
and realistic testing of military equipment, vehicles, weapons, and
sensors for proper operation and suitability for combat use by
providing critical data on the changing natural and physical
environment in which such materiel will be assessed and deployed. This
proposed scientific research also directly supports fleet training and
operations by providing up to date information and data on the natural
and physical environment essential to training and operations.
National Environmental Policy Act
To comply with the National Environmental Policy Act of 1969 (NEPA;
42 U.S.C. 4321 et seq.) and NOAA Administrative Order (NAO) 216-6A,
NMFS must review our proposed action (i.e., the issuance of an
incidental harassment authorization) with respect to potential impacts
on the human environment.
Accordingly, NMFS plans to adopt the Navy's Environmental
Assessment/Overseas Environmental Assessment, provided our independent
evaluation of the document finds that it includes adequate information
analyzing the effects on the human environment of issuing the IHA. The
Navy's OEA is available at https://www.fisheries.noaa.gov/permit/incidental-take-authorizations-under-marine-mammal-protection-act.
We will review all comments submitted in response to this notice
prior to concluding our NEPA process or making a final decision on the
IHA request.
Summary of Request
On April 25, 2019, NMFS received a request from ONR for an IHA to
take marine mammals incidental to Arctic Research Activities in the
Beaufort and Chukchi Seas. The application was deemed adequate and
complete on July 16, 2019. ONR's request is for take of a small number
of beluga whales (Delphinapterus leucas), bearded seals (Erignathus
barbatus), and ringed seals (Pusa hispida hispida) by Level B
harassment only. Neither ONR nor NMFS expects serious injury or
mortality to result from this activity and, therefore, an IHA is
appropriate.
This proposed IHA would cover the second year of a larger project
for which ONR obtained a prior IHA and intends to request take
authorization for subsequent facets of the project. This IHA would be
valid for a period of one year from the date of issuance. The larger
three-year project involves several scientific objectives which support
the Arctic and Global Prediction Program, as well as the Ocean
Acoustics Program and the Naval Research Laboratory, for which ONR is
the parent command. ONR complied with all the requirements (e.g.,
mitigation, monitoring, and reporting) of the previous IHA (83 FR
48799; September 27, 2019).
Description of Proposed Activity
Overview
ONR's Arctic Research Activities include scientific experiments to
be conducted in support of the programs named above. Specifically, the
project includes the Stratified Ocean Dynamics of the Arctic (SODA),
Arctic Mobile Observing System (AMOS), Ocean Acoustics field work
(including the Coordinated Arctic Active Tomography Experiment
(CAATEX)), and Naval Research Laboratory experiments in the Beaufort
and Chukchi Seas. These experiments involve deployment of moored and
ice-tethered active acoustic sources, primarily from the U.S Coast
Guard Cutter (CGC) HEALY. CGC HEALY may also be required to perform
icebreaking to deploy the acoustic sources in deep water. Underwater
sound from the acoustic sources and icebreaking may result in
behavioral harassment of marine mammals.
Dates and Duration
ONR's Arctic Research Activities began in August 2018 with
deployment of autonomous gliders in the Beaufort and Chukchi Seas and
subsequent deployment of moored acoustic sources in September 2018. The
activities analyzed in this proposed IHA would begin in September 2019,
with a tentative sail date of September 3, 2019. CGC HEALY would
perform a research cruise for up to 60 days in September and October
2019 to deploy acoustic sources. If required, a second, non-icebreaking
ship would perform a cruise of up to 30 days to deploy any remaining
sources in the fall of 2019. A total of eight days of icebreaking
within the effective dates of this IHA are anticipated to be required
to deploy and/or retrieve the northernmost acoustic sources. CGC HEALY,
a similar icebreaking ship, or a non-icebreaking ship would be used for
a subsequent research cruise for up to 60 days beginning in August
2020. The initial stages of the August 2020 cruise (i.e., the spiral
wave beacon, see Detailed Description of Specific Activity below) are
included in the activities analyzed in this IHA. The latter stages of
the 2020 cruise would be analyzed in a subsequent IHA
Specific Geographic Region
The proposed actions would occur in either the U.S. Exclusive
Economic Zone (EEZ) or the high seas north of Alaska (Figure 1). All
activities, except for the transit of ships, would take place outside
U.S. territorial waters. The total area of the study area is 835,860
square kilometers (km\2\) (322,727 square miles (mi\2\)). The closest
active acoustic source (aside from de minimis sources described below)
within the study area is approximately 145 miles (mi; 233 kilometers
(km)) from land.
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Figure 1. Arctic Research Activities Study Area
Detailed Description of Specific Activity
The ONR Arctic and Global Prediction Program is supporting two
major projects (SODA and AMOS), which will both occur during time
period covered by this IHA. The SODA project began field work in August
2018, consisting of research cruises and the deployment of autonomous
[[Page 37243]]
measurement devices for year-round observation of water properties
(temperature and salinity) and the associated stratification and
circulation. These physical processes are related to the ice cover and
as the properties of the ice cover change, the water properties will
change as well. Warm water feeding into the Arctic Ocean also plays an
important role changing the environment. Observations of these
phenomena require geographical sampling of areas of varying ice cover
and temperature profile, and year-round temporal sampling to understand
what happens during different parts of the year. Unmanned gliders and
autonomous platforms are needed for this type of year-round observation
of a representative sample of arctic waters. The SODA project also
involved the initial deployment of navigation sources for unmanned
vehicles. Under the AMOS project, there will be new deployments of
navigation sources in September 2019 (Figure 1). Geolocation of
autonomous platforms requires the use of acoustic navigation signals,
and therefore, year-long use of active acoustic signals.
The ONR Ocean Acoustics Program also supports Arctic field work.
The emphasis of the Ocean Acoustics Program field efforts is to
understand how the changing environment affects acoustic propagation
and the noise environment. The ONR Acoustic Program would be utilizing
new technology for year-round observation of the large-scale (range and
depth) temperature structure of the ocean at very low frequencies. The
use of specialized waveforms and acoustic arrays allows signals to be
received over 100 km from a source, while only requiring moderate
source levels. The Ocean Acoustics program is planning to perform
experiments in conjunction with the Arctic and Global Prediction
Program by operating in the same general location and with the same
research vessel.
The Naval Research Laboratory would also conduct Arctic research in
the same time frame, using drifting buoys with active acoustic sources
that are deployed in the ice. The buoys are deployed for real-time
environmental characterization to aid in mid-frequency sonar
performance predictions. Real-time assimilation of acoustic data into
an ocean model is also planned.
Below are descriptions of the equipment and platforms that would be
deployed at different times during the proposed action.
Research Vessels
CGC HEALY would be the primary vessel performing the research
cruise in September and October 2019. CGC HEALY travels at a maximum
speed of 17 knots (kn) with a cruising speed of 12 kn (United States
Coast Guard 2013), and a maximum speed of 3 kn when traveling through
3.5 feet (ft; 1.07 meters (m)) of sea ice (Murphy 2010). CGC HEALY may
be required to perform icebreaking to deploy the moored and ice
tethered acoustic sources in deep water. Icebreaking would only occur
during the warm season, presumably in the August through October
timeframe. CGC HEALY has proven capable of breaking ice up to 8 ft (2.4
m) thick while backing and ramming (Roth et al. 2013). A study in the
western Arctic Ocean was conducted while CGC HEALY was mapping the
seafloor north of the Chukchi Cap in August 2008. During this study,
CGC HEALY icebreaker events generated signals with frequency bands
centered near 10, 50, and 100 Hertz (Hz) with maximum source levels of
190 to 200 decibel(s) (dB) referenced to 1 microPascal ([micro]Pa) at 1
meter (dB re 1 [micro]Pa at 1 m; full octave band) (Roth et al. 2013).
Icebreaking would likely only occur in the northernmost areas of the
study area while deploying and/or retrieving sources.
The CGC HEALY or other vessels may perform the following activities
during the research cruises (some of these activities may result in
take of marine mammals, while others may not, as described further
below):
Deployment of moored and/or ice-tethered passive sensors
(e.g., oceanographic measurement devices, acoustic receivers);
Deployment of moored and/or ice-tethered active acoustic
sources to transmit acoustic signals for up to two years after
deployment. Transmissions could be terminated during ice-free periods
(August-October) each year, if needed;
Deployment of unmanned surface, underwater, and air
vehicles; and
Recovery of equipment.
Additional oceanographic measurements would be made using ship-
based systems, including the following:
Modular Microstructure Profiler, a tethered profiler that
would measure oceanographic parameters within the top 984 ft (300 m) of
the water column;
Shallow Water Integrated Mapping System, a winched towed
body with a Conductivity Temperature Depth sensor, upward and downward
looking Acoustic Doppler Current Profilers (ADCPs), and a temperature
sensor within the top 328 ft (100 m) of the water column;
Three-dimensional Sonic Anemometer, which would measure
wind stress from the foremast of the ship;
Surface Wave Instrument Float with Tracking (SWIFTs) buoys
are freely drifting buoys measuring winds, waves, and other parameters
with deployments spanning from hours to days; and
A single mooring would be deployed to perform measurements
of currents with an ADCP.
Moored and Drifting Acoustic Sources
Up to 15 moored acoustic navigation sources would be deployed
during the period September 2019 to September 2020 at the locations
shown in Figure 1. Each navigation source transmits for 8 seconds every
4 hours, with the sources transmitting with a five minute offset from
each other. The purpose of the navigation sources is to allow
autonomous vehicles and gliders to navigate by receiving acoustic
signals from multiple locations and triangulating position. This is
needed for vehicles that are under ice and cannot communicate with
satellites.
A single very low frequency (VLF) source would be deployed in the
furthest north part of the study area, shown by the triangle symbols in
Figure 1. The northernmost location is the preferred location, but the
alternative location may be used. The VLF source provides capability
for persistent (year-long) observation of Arctic oceanographic
processes and measures oceanographic changes (e.g. regional increases
in temperature) over long ranges.
All moorings would be anchored on the seabed and held in the water
column with subsurface buoys. All sources would be deployed by
shipboard winches, which would lower sources and receivers in a
controlled manner. Anchors would be steel ``wagon wheels'' typically
used for this type of deployment.
Up to six drifting sources would be deployed for the purpose of
near-real time environmental characterization, which is accomplished by
communicating information from the drifting buoys to a satellite. They
would be deployed in the ice for purposes of buoy stability, but would
eventually drift in open water. The sources would transmit signals to
each other to measure oceanographic properties of the water between
them. The sources would stop transmitting when this IHA expires in
September 2020 or when they leave the Study Area, whichever comes
first.
[[Page 37244]]
On the fall 2020 cruise, a spiral wave beacon source would be
tested for fine-scale navigation. The spiral wave beacon is a mid-
frequency source that transmits a 50 millisecond signal at 30 second
intervals. The source would be deployed from a ship at a single
location and transmit for up to 5 days. It will either be attached to
the ship or moored near the ship. The ship will remain for the 5 days
of the test, and the source will be recovered at the end of testing.
Table 1--Characteristics of Proposed Acoustic Sources
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sound pressure level
Source name Frequency (dB re 1 [micro]Pa at 1 Pulse length Duty cycle Source type Usage
range (Hz) m) (milliseconds) (percent)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Navigation Sources.................. 900 185.................... 8,000 <1 Moored................. 15 sources
transmitting 8
seconds every 4
hours, up to 2 years.
Real-Time Sensing Sources........... 900 to 1000 184.................... 60,000 <1 Drifting............... 6 sources transmitting
1 minute every 4
hours, up to 2 years.
Spiral Wave Beacon.................. 2,500 183.................... 50 <1 Moored................. 5 days.
Very Low Frequency (VLF source)..... 34 185 (peak)............. 1,800,000 <1 Moored................. One source
transmitting 30
minutes every 6 days,
up to 2 years.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Activities Not Likely to Result in Take
The following in-water activities have been determined to be
unlikely to result in take of marine mammals. These activities are
described here but their effects are not described further in this
document.
De minimis Sources--De minimis sources have the following
parameters: Low source levels, narrow beams, downward directed
transmission, short pulse lengths, frequencies outside known marine
mammal hearing ranges, or some combination of these factors (Department
of the Navy 2013b). For further detail regarding the de minimis sources
planned for use by the Navy, which are not quantitatively analyzed,
please see the Navy's application. Descriptions of example sources are
provided below and in Table 2.
Table 2--Parameters for De Minimis Sources
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sound
pressure Pulse
Source name Frequency range (kHz) level (dB length Duty cycle Beamwidth De minimis
re 1 [mu]Pa (milli- (percent) justification
at 1 m) seconds)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Pressure Inverted Echosounders (PIES) 12...................... 170-180 6 <0.01 45..................... Extremely low duty
cycle, low source
level, very short
pulse length.
ADCP................................. >200, 150, or 75........ 190 <1 <0.1 2.2.................... Very low pulse length,
narrow beam, moderate
source level.
Chirp sonar.......................... 2-16.................... 200 20 <1 narrow................. Very short pulse
length, low duty
cycle, narrow beam
width.
Expendable Mobile Anti-Submarine 700-1100 Hz and 1100- <150 N/A 25-100 Omni................... Very low source level.
Warfare Training Targets (EMATTs). 4000 Hz.
Coring system........................ 25-200.................. 158-162 <1 16 Omni................... Very low source
level.\2\
CTD\1\ attached Echosounder.......... 5-20.................... 160 4 2 Omni................... Very low source level.
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ CTD = Conductivity Temperature Depth.
\2\ Within sediment, not within the water column.
Drifting Oceanographic Sensors--Observations of ocean-ice
interactions require the use of sensors which are moored and embedded
in the ice. Sensors are deployed within a few dozen meters of each
other on the same ice floe. Three types of sensors would be used:
Autonomous Ocean Flux Buoys, Integrated Autonomous Drifters, and Ice
Tethered Profilers. The autonomous ocean flux buoys measure
oceanographic properties just below the ocean-ice interface. The
autonomous ocean flux buoys would have ADCPs and temperature chains
attached, to measure temperature, salinity, and other ocean parameters
in the top 20 ft (6 m) of the water column. Integrated Autonomous
Drifters would have a long temperature string extending down to 656 ft
(200 m) depth and would incorporate meteorological sensors, and a
temperature string to estimate ice thickness. The Ice Tethered
Profilers would collect information on ocean temperature, salinity, and
velocity down to 820 ft (250 m) depth.
Fifteen autonomous floats (Air-Launched Autonomous Micro Observers)
would be deployed during the proposed action to measure seasonal
evolution of the ocean temperature and salinity, as well as currents.
They would be deployed on the eastern edge of the Chukchi Sea in water
less than 3,280 ft (1,000 m) deep. Three autonomous floats would act as
virtual moorings by originating on the seafloor, then moving up the
water column to the surface and returning to the seafloor. The other 12
autonomous floats would sit on the sea floor and at intervals begin to
move toward the surface. At programmed intervals, a subset of the
floats would release anchors and begin their profiling mission. Up to
15 additional floats may be deployed by ships of opportunity in the
Beaufort Gyre.
The drifting oceanographic sensors described above use only de
minimis sources and are therefore not anticipated to have the potential
for impacts on marine mammals or their habitat.
Moored Oceanographic Sensors--Moored sensors would capture a range
of ice, ocean, and atmospheric conditions on a year-round basis. The
location of the bottom-anchored sub-surface moorings are depicted by
the purple stars in Figure 1-1 of the IHA application. These would be
bottom-anchored, sub-surface moorings measuring velocity, temperature,
and salinity in the upper 1,640 ft (500 m) of the water column. The
moorings also collect high-resolution acoustic measurements of the ice
using the ice profilers described above. Ice velocity
[[Page 37245]]
and surface waves would be measured by 500 kHz multibeam sonars.
Additionally, Beaufort Gyre Exploration Project moorings BGOS-A and
BGOS-B (depicted by the black plus signs in Figure 1-1 of the IHA
application) would be augmented with McLane Moored Profilers. BGOS-A
and BGOS-B would provide measurements near the Northwind Ridge, with
considerable latitudinal distribution. Existing deployments of Nortek
Acoustic Wave and Current Profilers on BGOS-A and BGOS-B would also be
continued as part of the proposed action.
The moored oceanographic sensors described above use only de
minimis sources and are therefore not anticipated to have the potential
for impacts on marine mammals or their habitat.
Fixed and Towed Receiving Arrays--Horizontal and vertical arrays
may be used to receive acoustic signals. Two receiving arrays will be
deployed in September-October 2020 to receive signals from the CAATEX
source. Other receiving arrays are the Single Hydrophone Recording
Units and Autonomous Multichannel Acoustic Recorder. All these arrays
would be moored to the seafloor and remain in place throughout the
activity.
These are passive acoustic sensors and therefore are not
anticipated to have the potential for impacts on marine mammals or
their habitat.
Activities Involving Aircraft and Unmanned Air Vehicles--Naval
Research Laboratory would be conducting flights to characterize the ice
structure and character, ice edge and wave heights across the open
water and marginal ice zone to the ice. Up to 4 flights, lasting
approximately 3 hours in duration would be conducted over a 10 day
period during February or March for ice structure and character
measurements and during late summer/early fall for ice edge and wave
height studies. Flights would be conducted with a Twin Otter aircraft
over the seafloor mounted acoustic sources and receivers. Most flights
would transit at 1,500 ft or 10,000 ft (457 or 3,048 m) above sea
level. Twin Otters have a typical survey speed of 90 to 110 kn, 66 ft
(20 m) wing span, and a total length of 26 ft (8 m) (U.S. Department of
Commerce and NOAA 2015). At a distance of 2,152 ft (656 m) away, the
received pressure levels of a Twin Otter range from 80 to 98.5 A-
weighted dB (expression of the relative loudness in the air as
perceived by the human ear) and frequency levels ranging from 20 Hz to
10 kHz, though they are more typically in the 500 Hz range (Metzger
1995). The objective of the flights is to characterize thickness and
physical properties of the ice mass overlying the experiment area.
Rotary wing aircraft may also be used during the activity.
Helicopter transit would be no longer than two hours to and from the
ice location. A twin engine helicopter may be used to transit
scientists from land to an offshore floating ice location. Once on the
floating ice, the team would drill holes with up to a 10 inch (in; 25.4
centimeter (cm)) diameter to deploy scientific equipment (e.g., source,
hydrophone array, EMATT) into the water column. The science team would
depart the area and return to land after three hours of data collection
and leave the equipment and leave the equipment behind for a later
recovery.
The proposed action includes the use of an Unmanned Aerial System
(UAS). The UAS would be deployed ahead of the ship to ensure a clear
passage for the vessel and would have a maximum flight time of 20
minutes. The UAS would not be used for marine mammal observations or
hover close to the ice near marine mammals. The UAS that would be used
during the proposed action is a small commercially available system
that generates low sound levels and is smaller than military grade
systems. The dimensions of the proposed UAS are, 11.4 in (29 cm) by
11.4 in (29 cm) by 7.1 in (18 cm) and weighs 2.5 lb (1.13 kg). The UAS
can operate up to 984 ft (300 m) away, which would keep the device in
close proximity to the ship. The planned operation of the UAS is to fly
it vertically above the ship to examine the ice conditions in the path
of the ship and around the area (i.e., not flown at low altitudes
around the vessel). Currently acoustic parameters are not available for
the proposed models of UASs to be used. As stated previously, these
systems are small and are similar to a remote control helicopter. It is
likely marine mammals would not hear the device since the noise
generated would likely not be audible from greater than 5 ft (1.5 m)
away (Christiansen et al., 2016).
All aircraft (manned and unmanned) would be required to maintain a
minimum separation distance of 1,000 ft (305 m) from any pinnipeds
hauled out on the ice. Therefore, no take of marine mammals is
anticipated from these activities.
On-Ice Measurement Systems--On-ice measurement systems would be
used to collect weather data. These would include an Autonomous Weather
Station and an Ice Mass Balance Buoy. The Autonomous Weather Station
would be deployed on a tripod; the tripod has insulated foot platforms
that are frozen into the ice. The system would consist of an
anemometer, humidity sensor, and pressure sensor. The Autonomous
Weather Station also includes an altimeter that is de minimis due to
its very high frequency (200 kHz). The Ice Mass Balance Buoy is a 20 ft
(6 m) sensor string, which is deployed through a 2 in (5 cm) hole
drilled into the ice. The string is weighted by a 2.2 lb (1 kg) lead
weight, and is supported by a tripod. The buoy contains a de minimis
200 kHz altimeter and snow depth sensor. Autonomous Weather Stations
and Ice Mass Balance Buoys will be deployed, and will drift with the
ice, making measurements, until their host ice floes melt, thus
destroying the instruments (likely in summer, roughly one year after
deployment). After the on-ice instruments are destroyed they cannot be
recovered, and would sink to the seafloor as their host ice floes
melted.
All personnel conducting experiments on the ice would be required
to maintain a minimum separation distance of 1,000 ft (305 m) from any
pinnipeds hauled out on the ice. Therefore, no take of marine mammals
is anticipated from these activities.
Bottom Interaction Systems--Coring of bottom sediment could occur
anywhere within the study area to obtain a more complete understanding
of the Arctic environment. Coring equipment would take up to 50 samples
of the ocean bottom in the study area annually. The samples would be
roughly cylindrical, with a 3.1 in (8 cm) diameter cross-sectional
area; the corings would be between 10 and 20 ft (3 and 6 m) long.
Coring would only occur during research cruises, during the summer or
early fall. The coring equipment moves slowly through the muddy bottom,
at a speed of approximately 1 m per hour, and would not create any
detectable acoustic signal within the water column, though very low
levels of acoustic transmissions may be created in the mud (see
parameters listed in Table 2).
Weather Balloons--To support weather observations, up to 40 Kevlar
or latex balloons would be launched per year for the duration of the
proposed action. These balloons and associated radiosondes (a sensor
package that is suspended below the balloon) are similar to those that
have been deployed by the National Weather Service since the late
1930s. When released, the balloon is approximately 5 to 6 ft (1.5-1.8
m) in diameter and gradually expands as it rises due to the decrease in
air pressure. When the balloon
[[Page 37246]]
reaches a diameter of 13-22 ft (4-7 m), it bursts and a parachute is
deployed to slow the descent of the associated radiosonde. Weather
balloons would not be recovered.
The deployment of weather balloons does not include the use of
active acoustics and is therefore not anticipated to have the potential
for impacts on marine mammals or their habitat.
Proposed mitigation, monitoring, and reporting measures are
described in detail later in this document (please see Proposed
Mitigation and Proposed Monitoring and Reporting).
Description of Marine Mammals in the Area of Specified Activities
Sections 3 and 4 of the application summarize available information
regarding status and trends, distribution and habitat preferences, and
behavior and life history, of the potentially affected species.
Additional information regarding population trends and threats may be
found in NMFS's Stock Assessment Reports (SARs; https://www.fisheries.noaa.gov/national/marine-mammal-protection/marine-mammal-stock-assessments) and more general information about these species
(e.g., physical and behavioral descriptions) may be found on NMFS's
website (https://www.fisheries.noaa.gov/find-species).
Table 3 lists all species with expected potential for occurrence in
the study area and summarizes information related to the population or
stock, including regulatory status under the MMPA and ESA and potential
biological removal (PBR), where known. For taxonomy, we follow
Committee on Taxonomy (2018). PBR is defined by the MMPA as the maximum
number of animals, not including natural mortalities, that may be
removed from a marine mammal stock while allowing that stock to reach
or maintain its optimum sustainable population (as described in NMFS's
SARs). While no mortality is anticipated or authorized here, PBR and
annual serious injury and mortality from anthropogenic sources are
included here as gross indicators of the status of the species and
other threats.
Marine mammal abundance estimates presented in this document
represent the total number of individuals that make up a given stock or
the total number estimated within a particular study or survey area.
NMFS's stock abundance estimates for most species represent the total
estimate of individuals within the geographic area, if known, that
comprises that stock. For some species, this geographic area may extend
beyond U.S. waters. All managed stocks in this region are assessed in
NMFS's U.S. 2018 SARs (e.g., Muto et al., 2019, Carretta et al., 2019).
All values presented in Table 3 are the most recent available at the
time of publication and are available in the 2018 SARs (Muto et al.,
2019; Carretta et al., 2019).
Table 3--Marine Mammal Species Potentially Present in the Project Area
--------------------------------------------------------------------------------------------------------------------------------------------------------
ESA/MMPA status; Stock abundance (CV,
Common name Scientific name Stock strategic (Y/N) Nmin, most recent PBR Annual M/
\1\ abundance survey) \2\ SI \3\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Order Cetartiodactyla--Cetacea--Superfamily Mysticeti (baleen whales)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Eschrichtiidae:
Gray whale...................... Eschrichtius robustus.. Eastern North Pacific.. -/- ; N 26960 (0.05, 25,849, 801 135
2016).
Family Balaenidae:
Bowhead whale................... Balaena mysticetus..... Western Arctic......... E/D ; Y 16,820 (0.052, 16,100, 161 46
2011).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Superfamily Odontoceti (toothed whales, dolphins, and porpoises)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Delphinidae:
Beluga whale.................... Delphinapterus leucas.. Beaufort Sea........... -/- ; N 39,258 (0.229, N/A, \4\ Undet 139
1992).
Beluga whale.................... Delphinapterus leucas.. Eastern Chukchi Sea.... -/- ; N 20,752 (0.70, 12.194, 244 67
2012).
--------------------------------------------------------------------------------------------------------------------------------------------------------
Order Carnivora--Superfamily Pinnipedia
--------------------------------------------------------------------------------------------------------------------------------------------------------
Family Phocidae (earless seals):
Bearded seal \5\................ Erignathus barbatus.... Alaska................. T/D ; Y 299,174............... 8,210 557
(-, 273,676, 2013)....
Ribbon seal..................... Histriophoca fasciata.. Alaska................. -/- ; N 184,697............... 9,785 3.9
(-, 163,086, 2013)....
Ringed seal \5\................. Pusa hispida hispida... Alaska................. T/D ; Y 170,000............... 5,100 1,054
(-, 170,000, 2013)....
Spotted seal.................... Phoca largha........... Alaska................. -/- ; N 461,625............... 12,697 329
(-, 423,237, 2013)....
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ Endangered Species Act (ESA) status: Endangered (E), Threatened (T)/MMPA status: Depleted (D). A dash (-) indicates that the species is not listed
under the ESA or designated as depleted under the MMPA. Under the MMPA, a strategic stock is one for which the level of direct human-caused mortality
exceeds PBR or which is determined to be declining and likely to be listed under the ESA within the foreseeable future. Any species or stock listed
under the ESA is automatically designated under the MMPA as depleted and as a strategic stock.
\2\ NMFS marine mammal stock assessment reports online at: https://www.fisheries.noaa.gov/national/marine-mammal-protection/marine-mammal-stock-assessment-reports-region/. CV is coefficient of variation; Nmin is the minimum estimate of stock abundance. In some cases, CV is not applicable.
\3\ These values, found in NMFS's SARs, represent annual levels of human-caused mortality plus serious injury from all sources combined (e.g.,
commercial fisheries, ship strike). Annual M/SI often cannot be determined precisely and is in some cases presented as a minimum value or range. A CV
associated with estimated mortality due to commercial fisheries is presented in some cases.
\4\ The 2016 guidelines for preparing SARs state that abundance estimates older than 8 years should not be used to calculate PBR due to a decline in the
reliability of an aged estimate. Therefore, the PBR for this stock is considered undetermined.
\5\ Abundances and associated values for bearded and ringed seals are for the U.S. population in the Bering Sea only.
Note: Italicized species are not expected to be taken or proposed for authorization.
All species that could potentially occur in the proposed survey
areas are included in Table 3. Activities conducted during the proposed
action are expected to cause harassment, as defined by the MMPA as it
applies to military readiness, to the beluga whale (of the Beaufort and
Eastern Chukchi Sea stocks), bearded seal, and ringed seal. Due to the
location of the study area (i.e., northern offshore, deep water), there
were no calculated exposures for
[[Page 37247]]
the bowhead whale, gray whale, spotted seal, and ribbon seal from
quantitative modeling of non-impulsive acoustic and icebreaking
sources. Bowhead and gray whales remain closely associated with the
shallow waters of the continental shelf in the Beaufort Sea and are
unlikely to be exposed to acoustic harassment (Carretta et al., 2017;
Muto et al., 2018). Similarly, spotted seals tend to prefer pack ice
areas with water depths less than 200 m during the spring and move to
coastal habitats in the summer and fall, found as far north as 69-
72[deg] N (Muto et al., 2018). Although the study area includes waters
south of 72[deg] N, the acoustic sources with the potential to result
in take of marine mammals are not found below that latitude and spotted
seals are not expected to be exposed. Ribbon seals are found year-round
in the Bering Sea but may seasonally range into the Chukchi Sea (Muto
et al., 2018). The proposed action occurs primarily in the Beaufort
Sea, outside of the core range of ribbon seals, thus ribbon seals are
not expected to be behaviorally harassed. Narwhals are considered
extralimital in the project area and are not expected to be encountered
or taken. As no harassment is expected of bowhead whales, gray whales,
spotted seals, and ribbon seals, these species will not be discussed
further in this IHA.
Beluga Whale
Beluga whales are distributed throughout seasonally ice-covered
arctic and subarctic waters of the Northern Hemisphere (Gurevich 1980),
and are closely associated with open leads and polynyas in ice-covered
regions (Hazard 1988). Belugas are both migratory and residential (non-
migratory), depending on the population. Seasonal distribution is
affected by ice cover, tidal conditions, access to prey, temperature,
and human interaction (Frost et al., 1985).
There are five beluga stocks recognized within U.S. waters: Cook
Inlet, Bristol Bay, eastern Bering Sea, eastern Chukchi Sea, and
Beaufort Sea. Two stocks, the Beaufort Sea and eastern Chukchi Sea
stocks, have the potential to occur in the Study Area.
There are two migration areas used by Beaufort Sea belugas that
overlap the Study Area. One, located in the Eastern Chukchi and Alaskan
Beaufort Sea, is a migration area in use from April to May. The second,
located in the Alaskan Beaufort Sea, is used by migrating belugas from
September to October (Calambokidis et al., 2015). During the winter,
they can be found foraging in offshore waters associated with pack ice.
When the sea ice melts in summer, they move to warmer river estuaries
and coastal areas for molting and calving (Muto et al., 2017). Annual
migrations can span over thousands of kilometers. The residential
Beaufort Sea populations participate in short distance movements within
their range throughout the year. Based on satellite tags (Suydam et
al., 2001) there is some overlap in distribution with the eastern
Chukchi Sea beluga whale stock.
During the winter, eastern Chukchi Sea belugas occur in offshore
waters associated with pack ice. In the spring, they migrate to warmer
coastal estuaries, bays, and rivers where they may molt (Finley 1982;
Suydam 2009) and give birth to and care for their calves (Sergeant and
Brodie 1969). Eastern Chukchi Sea belugas move into coastal areas,
including Kasegaluk Lagoon (outside of the Study Area), in late June
and animals are sighted in the area until about mid-July (Frost and
Lowry 1990; Frost et al., 1993). Satellite tags attached to eastern
Chukchi Sea belugas captured in Kaseguluk Lagoon during the summer
showed these whales traveled 593 nm (1,100 km) north of the Alaska
coastline, into the Canadian Beaufort Sea within three months (Suydam
et al., 2001). Satellite telemetry data from 23 whales tagged during
1998-2007 suggest variation in movement patterns for different age and/
or sex classes during July-September (Suydam et al., 2005). Adult males
used deeper waters and remained there for the duration of the summer;
all belugas that moved into the Arctic Ocean (north of 75[deg] N) were
males, and males traveled through 90 percent pack ice cover to reach
deeper waters in the Beaufort Sea and Arctic Ocean (79-80[deg] N) by
late July/early August. Adult and immature female belugas remained at
or near the shelf break in the south through the eastern Bering Strait
into the northern Bering Sea, remaining north of Saint Lawrence Island
over the winter. A whale tagged in the eastern Chukchi Sea in 2007
overwintered in the waters north of Saint Lawrence Island during 2007/
2008 and moved to near King Island in April and May before moving north
through the Bering Strait in late May and early June (Suydam 2009).
Bearded Seal
Bearded seals are a boreoarctic species with circumpolar
distribution (Burns 1967; Burns 1981; Burns and Frost 1979; Fedoseev
1965; Johnson et al., 1966; Kelly 1988a; Smith 1981). Their normal
range extends from the Arctic Ocean (85[deg] N) south to Sakhalin
Island (45[deg] N) in the Pacific and south to Hudson Bay (55[deg] N)
in the Atlantic (Allen 1880; King 1983; Ognev 1935). Bearded seals are
widely distributed throughout the northern Bering, Chukchi, and
Beaufort Seas and are most abundant north of the ice edge zone
(MacIntyre et al., 2013). Bearded seals inhabit the seasonally ice-
covered seas of the Northern Hemisphere, where they whelp and rear
their pups and molt their coats on the ice in the spring and early
summer. The overall summer distribution is quite broad, with seals
rarely hauled out on land, and some seals, mostly juveniles, may not
follow the ice northward but remain near the coasts of Bering and
Chukchi seas (Burns 1967; Burns 1981; Heptner et al., Nelson 1981). As
the ice forms again in the fall and winter, most seals move south with
the advancing ice edge through the Bering Strait into the Bering Sea
where they spend the winter (Boveng and Cameron 2013; Burns and Frost
1979; Cameron and Boveng 2007; Cameron and Boveng 2009; Frost et al.,
2005; Frost et al., 2008). This southward migration is less noticeable
and predictable than the northward movements in late spring and early
summer (Burns 1981; Burns and Frost 1979; Kelly 1988a). During winter,
the central and northern parts of the Bering Sea shelf have the highest
densities of bearded seals (Braham et al., 1981; Burns 1981; Burns and
Frost 1979; Fay 1974; Heptner et al., 1976; Nelson et al., 1984). In
late winter and early spring, bearded seals are widely but not
uniformly distributed in the broken, drifting pack ice ranging from the
Chukchi Sea south to the ice front in the Bering Sea. In these areas,
they tend to avoid the coasts and areas of fast ice (Burns 1967; Burns
and Frost 1979).
Bearded seals along the Alaskan coast tend to prefer areas where
sea ice covers 70 to 90 percent of the surface, and are most abundant
20 to 100 nautical miles (nmi) (37 to 185 (km) offshore during the
spring season (Bengston et al., 2000; Bengston et al., 2005; Simpkins
et al., 2003). In spring, bearded seals may also concentrate in
nearshore pack ice habitats, where females give birth on the most
stable areas of ice (Reeves et al., 2003) and generally prefer to be
near polynyas (areas of open water surrounded by sea ice) and other
natural openings in the sea ice for breathing, hauling out, and prey
access (Nelson et al., 1984; Stirling 1997). While molting between
April and August, bearded seals spend substantially more time hauled
out than at other times of the year (Reeves et al., 2002).
In their explorations of the Canada Basin, Harwood et al. (2005)
observed bearded seals in waters of less than 656 ft (200 m) during the
months from August to September. These sightings were east of 140[deg]
W. The Bureau of
[[Page 37248]]
Ocean Energy Management conducted an aerial survey from June through
October that covered the shallow Beaufort and Chukchi Sea shelf waters,
and observed bearded seals from Point Barrow to the border of Canada
(Clarke et al., 2014). The farthest from shore that bearded seals were
observed was the waters of the continental slope.
On December 28, 2012, NMFS listed both the Okhotsk and the Beringia
distinct population segments (DPSs) of bearded seals as threatened
under the ESA (77 FR 76740). The Alaska stock of bearded seals consists
of only Beringia DPS seals.
Ringed Seal
Ringed seals are the most common pinniped in the Study Area and
have wide distribution in seasonally and permanently ice-covered waters
of the Northern Hemisphere (North Atlantic Marine Mammal Commission
2004). Throughout their range, ringed seals have an affinity for ice-
covered waters and are well adapted to occupying both shore-fast and
pack ice (Kelly 1988c). Ringed seals can be found further offshore than
other pinnipeds since they can maintain breathing holes in ice
thickness greater than 6.6 ft (2 m) (Smith and Stirling 1975).
Breathing holes are maintained by ringed seals' sharp teeth and claws
on their fore flippers. They remain in contact with ice most of the
year and use it as a platform for molting in late spring to early
summer, for pupping and nursing in late winter to early spring, and for
resting at other times of the year (Muto et al., 2017).
Ringed seals have at least two distinct types of subnivean lairs:
Haulout lairs and birthing lairs (Smith and Stirling 1975). Haulout
lairs are typically single-chambered and offer protection from
predators and cold weather. Birthing lairs are larger, multi-chambered
areas that are used for pupping in addition to protection from
predators. Ringed seals pup on both land-fast ice as well as stable
pack ice. Lentfer (1972) found that ringed seals north of Barrow,
Alaska build their subnivean lairs on the pack ice near pressure
ridges. Since subnivean lairs were found north of Barrow, Alaska, in
pack ice, they are also assumed to be found within the sea ice in the
Study Area. Ringed seals excavate subnivean lairs in drifts over their
breathing holes in the ice, in which they rest, give birth, and nurse
their pups for 5-9 weeks during late winter and spring (Chapskii 1940;
McLaren 1958; Smith and Stirling 1975). Snow depths of at least 20-26
in (50-65 cm) are required for functional birth lairs (Kelly 1988b;
Lydersen 1998; Lydersen and Gjertz 1986; Smith and Stirling 1975), and
such depths typically are found only where 8-12 in (20-30 cm) or more
of snow has accumulated on flat ice and then drifted along pressure
ridges or ice hummocks (Hammill 2008; Lydersen et al., 1990; Lydersen
and Ryg 1991; Smith and Lydersen 1991). Ringed seals are born beginning
in March, but the majority of births occur in early April. About a
month after parturition, mating begins in late April and early May.
In Alaska waters, during winter and early spring when sea ice is at
its maximum extent, ringed seals are abundant in the northern Bering
Sea, Norton and Kotzebue Sounds, and throughout the Chukchi and
Beaufort seas (Frost 1985; Kelly 1988c). Passive acoustic monitoring of
ringed seals from a high frequency recording package deployed at a
depth of 787 ft (240 m) in the Chukchi Sea 65 nmi (120 km) north-
northwest of Barrow, Alaska detected ringed seals in the area between
mid-December and late May over the 4 year study (Jones et al., 2014).
With the onset of fall freeze, ringed seal movements become
increasingly restricted and seals will either move west and south with
the advancing ice pack with many seals dispersing throughout the
Chukchi and Bering Seas, or remaining in the Beaufort Sea (Crawford et
al., 2012; Frost and Lowry 1984; Harwood et al., 2012). Kelly et al.
(2010a) tracked home ranges for ringed seals in the subnivean period
(using shore-fast ice); the size of the home ranges varied from less
than 1 up to 279 km\2\ (median is 0.62 km\2\ for adult males and 0.65
km\2\ for adult females). Most (94 percent) of the home ranges were
less than 3 km\2\ during the subnivean period (Kelly et al., 2010a).
Near large polynyas, ringed seals maintain ranges, up to 7,000 km\2\
during winter and 2,100 km\2\ during spring (Born et al., 2004). Some
adult ringed seals return to the same small home ranges they occupied
during the previous winter (Kelly et al., 2010a). The size of winter
home ranges can, however, vary by up to a factor of 10 depending on the
amount of fast ice; seal movements were more restricted during winters
with extensive fast ice, and were much less restricted where fast ice
did not form at high levels (Harwood et al., 2015).
Most taxonomists recognize five subspecies of ringed seals. The
Arctic ringed seal subspecies occurs in the Arctic Ocean and Bering Sea
and is the only stock that occurs in U.S. waters (referred to as the
Alaska stock). NMFS listed the Arctic ringed seal subspecies as
threatened under the ESA on December 28, 2012 (77 FR 76706), primarily
due to anticipated loss of sea ice through the end of the 21st century.
Marine Mammal Hearing
Hearing is the most important sensory modality for marine mammals
underwater, and exposure to anthropogenic sound can have deleterious
effects. To appropriately assess the potential effects of exposure to
sound, it is necessary to understand the frequency ranges marine
mammals are able to hear. Current data indicate that not all marine
mammal species have equal hearing capabilities (e.g., Richardson et
al., 1995; Wartzok and Ketten, 1999; Au and Hastings, 2008). To reflect
this, Southall et al. (2007) recommended that marine mammals be divided
into functional hearing groups based on directly measured or estimated
hearing ranges on the basis of available behavioral response data,
audiograms derived using auditory evoked potential techniques,
anatomical modeling, and other data. Note that no direct measurements
of hearing ability have been successfully completed for mysticetes
(i.e., low-frequency cetaceans). Subsequently, NMFS (2018) described
generalized hearing ranges for these marine mammal hearing groups.
Generalized hearing ranges were chosen based on the approximately 65 dB
threshold from the normalized composite audiograms, with the exception
for lower limits for low-frequency cetaceans where the lower bound was
deemed to be biologically implausible and the lower bound from Southall
et al. (2007) retained. Marine mammal hearing groups and their
associated hearing ranges are provided in Table 4.
Table 4--Marine Mammal Hearing Groups
[NMFS, 2018]
----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Hearing group Generalized hearing range *
----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Low-frequency (LF) cetaceans (baleen whales)......... 7 Hz to 35 kHz.
[[Page 37249]]
Mid-frequency (MF) cetaceans (dolphins, toothed 150 Hz to 160 kHz.
whales, beaked whales, bottlenose whales).
High-frequency (HF) cetaceans (true porpoises, Kogia, 275 Hz to 160 kHz.
river dolphins, cephalorhynchid, Lagenorhynchus
cruciger & L. australis).
Phocid pinnipeds (PW) (underwater) (true seals)...... 50 Hz to 86 kHz.
Otariid pinnipeds (OW) (underwater) (sea lions and 60 Hz to 39 kHz.
fur seals).
----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
* Represents the generalized hearing range for the entire group as a composite (i.e., all species within the group), where individual species' hearing ranges are typically not as broad. Generalized hearing range chosen based on ~65 dB threshold from normalized composite audiogram, with the exception for lower limits for LF cetaceans (Southall et al.
2007) and PW pinniped (approximation).
The pinniped functional hearing group was modified from Southall et
al. (2007) on the basis of data indicating that phocid species have
consistently demonstrated an extended frequency range of hearing
compared to otariids, especially in the higher frequency range
(Hemil[auml] et al., 2006; Kastelein et al., 2009; Reichmuth and Holt,
2013).
For more detail concerning these groups and associated frequency
ranges, please see NMFS (2018) for a review of available information.
Three marine mammal species (one cetacean and two pinniped (both
phocid) species) have the reasonable potential to co-occur with the
proposed survey activities. Please refer to Table 3. Beluga whales are
classified as mid-frequency cetaceans.
Potential Effects of Specified Activities on Marine Mammals and Their
Habitat
This section includes a summary and discussion of the ways that
components of the specified activity may impact marine mammals and
their habitat. The Estimated Take by Incidental Harassment section
later in this document includes a quantitative analysis of the number
of individuals that are expected to be taken by this activity. The
Negligible Impact Analysis and Determination section considers the
content of this section, the Estimated Take by Incidental Harassment
section, and the Proposed Mitigation section, to draw conclusions
regarding the likely impacts of these activities on the reproductive
success or survivorship of individuals and how those impacts on
individuals are likely to impact marine mammal species or stocks.
Description of Sound Sources
Here, we first provide background information on marine mammal
hearing before discussing the potential effects of the use of active
acoustic sources on marine mammals.
Sound travels in waves, the basic components of which are
frequency, wavelength, velocity, and amplitude. Frequency is the number
of pressure waves that pass by a reference point per unit of time and
is measured in Hz or cycles per second. Wavelength is the distance
between two peaks of a sound wave; lower frequency sounds have longer
wavelengths than higher frequency sounds and attenuate (decrease) more
rapidly in shallower water. Amplitude is the height of the sound
pressure wave or the `loudness' of a sound and is typically measured
using the dB scale. A dB is the ratio between a measured pressure (with
sound) and a reference pressure (sound at a constant pressure,
established by scientific standards). It is a logarithmic unit that
accounts for large variations in amplitude; therefore, relatively small
changes in dB ratings correspond to large changes in sound pressure.
When referring to sound pressure levels (SPLs; the sound force per unit
area), sound is referenced in the context of underwater sound pressure
to 1 [mu]Pa. One pascal is the pressure resulting from a force of one
newton exerted over an area of one square meter. The source level (SL)
represents the sound level at a distance of 1 m from the source
(referenced to 1 [mu]Pa). The received level is the sound level at the
listener's position. Note that all underwater sound levels in this
document are referenced to a pressure of 1 [micro]Pa.
Root mean square (rms) is the quadratic mean sound pressure over
the duration of an impulse. RMS is calculated by squaring all of the
sound amplitudes, averaging the squares, and then taking the square
root of the average (Urick 1983). RMS accounts for both positive and
negative values; squaring the pressures makes all values positive so
that they may be accounted for in the summation of pressure levels
(Hastings and Popper 2005). This measurement is often used in the
context of discussing behavioral effects, in part because behavioral
effects, which often result from auditory cues, may be better expressed
through averaged units than by peak pressures.
When underwater objects vibrate or activity occurs, sound-pressure
waves are created. These waves alternately compress and decompress the
water as the sound wave travels. Underwater sound waves radiate in all
directions away from the source (similar to ripples on the surface of a
pond), except in cases where the source is directional. The
compressions and decompressions associated with sound waves are
detected as changes in pressure by aquatic life and man-made sound
receptors such as hydrophones.
Even in the absence of sound from the specified activity, the
underwater environment is typically loud due to ambient sound. Ambient
sound is defined as environmental background sound levels lacking a
single source or point (Richardson et al., 1995), and the sound level
of a region is defined by the total acoustical energy being generated
by known and unknown sources. These sources may include physical (e.g.,
waves, earthquakes, ice, atmospheric sound), biological (e.g., sounds
produced by marine mammals, fish, and invertebrates), and anthropogenic
sound (e.g., vessels, dredging, aircraft, construction). A number of
sources contribute to ambient sound, including the following
(Richardson et al., 1995):
Wind and waves: The complex interactions between wind and
water surface, including processes such as breaking waves and wave-
induced bubble oscillations and cavitation, are a main source of
naturally occurring ambient noise for frequencies between 200 Hz and 50
kHz (Mitson, 1995). Under sea ice, noise generated by ice deformation
and ice fracturing may be caused by thermal, wind, drift and current
stresses (Roth et al., 2012);
Precipitation: Sound from rain and hail impacting the
water surface can become an important component of total noise at
frequencies above 500 Hz, and possibly down to 100 Hz during quiet
times. In the ice-covered study area, precipitation is unlikely to
impact ambient sound;
[[Page 37250]]
Biological: Marine mammals can contribute significantly to
ambient noise levels, as can some fish and shrimp. The frequency band
for biological contributions is from approximately 12 Hz to over 100
kHz; and
Anthropogenic: Sources of ambient noise related to human
activity include transportation (surface vessels and aircraft),
dredging and construction, oil and gas drilling and production, seismic
surveys, sonar, explosions, and ocean acoustic studies. Shipping noise
typically dominates the total ambient noise for frequencies between 20
and 300 Hz. In general, the frequencies of anthropogenic sounds are
below 1 kHz and, if higher frequency sound levels are created, they
attenuate rapidly (Richardson et al., 1995). Sound from identifiable
anthropogenic sources other than the activity of interest (e.g., a
passing vessel) is sometimes termed background sound, as opposed to
ambient sound. Anthropogenic sources are unlikely to significantly
contribute to ambient underwater noise during the late winter and early
spring in the study area as most anthropogenic activities will not be
active due to ice cover (e.g. seismic surveys, shipping) (Roth et al.,
2012).
The sum of the various natural and anthropogenic sound sources at
any given location and time--which comprise ``ambient'' or
``background'' sound--depends not only on the source levels (as
determined by current weather conditions and levels of biological and
shipping activity) but also on the ability of sound to propagate
through the environment. In turn, sound propagation is dependent on the
spatially and temporally varying properties of the water column and sea
floor, and is frequency-dependent. As a result of the dependence on a
large number of varying factors, ambient sound levels can be expected
to vary widely over both coarse and fine spatial and temporal scales.
Sound levels at a given frequency and location can vary by 10-20 dB
from day to day (Richardson et al., 1995). The result is that,
depending on the source type and its intensity, sound from the
specified activity may be a negligible addition to the local
environment or could form a distinctive signal that may affect marine
mammals.
Underwater sounds fall into one of two general sound types:
Impulsive and non-impulsive (defined in the following paragraphs). The
distinction between these two sound types is important because they
have differing potential to cause physical effects, particularly with
regard to hearing (e.g., Ward, 1997 in Southall et al., 2007). Please
see Southall et al., (2007) for an in-depth discussion of these
concepts.
Impulsive sound sources (e.g., explosions, gunshots, sonic booms,
impact pile driving) produce signals that are brief (typically
considered to be less than one second), broadband, atonal transients
(ANSI 1986; Harris 1998; NIOSH 1998; ISO 2003; ANSI 2005) and occur
either as isolated events or repeated in some succession. Impulsive
sounds are all characterized by a relatively rapid rise from ambient
pressure to a maximal pressure value followed by a rapid decay period
that may include a period of diminishing, oscillating maximal and
minimal pressures, and generally have an increased capacity to induce
physical injury as compared with sounds that lack these features.
Non-impulsive sounds can be tonal, narrowband, or broadband, brief
or prolonged, and may be either continuous or non-continuous (ANSI
1995; NIOSH 1998). Some of these non-impulsive sounds can be transient
signals of short duration but without the essential properties of
pulses (e.g., rapid rise time). Examples of non-impulsive sounds
include those produced by vessels, aircraft, machinery operations such
as drilling or dredging, vibratory pile driving, and active sonar
sources that intentionally direct a sound signal at a target that is
reflected back in order to discern physical details about the target.
These active sources are used in navigation, military training and
testing, and other research activities such as the activities planned
by ONR as part of the proposed action. Icebreaking is also considered a
non-impulsive sound. The duration of such sounds, as received at a
distance, can be greatly extended in a highly reverberant environment.
Acoustic Impacts
Please refer to the information given previously regarding sound,
characteristics of sound types, and metrics used in this document.
Anthropogenic sounds cover a broad range of frequencies and sound
levels and can have a range of highly variable impacts on marine life,
from none or minor to potentially severe responses, depending on
received levels, duration of exposure, behavioral context, and various
other factors. The potential effects of underwater sound from active
acoustic sources can potentially result in one or more of the
following: temporary or permanent hearing impairment, non-auditory
physical or physiological effects, behavioral disturbance, stress, and
masking (Richardson et al., 1995; Gordon et al., 2004; Nowacek et al.,
2007; Southall et al., 2007; Gotz et al., 2009). The degree of effect
is intrinsically related to the signal characteristics, received level,
distance from the source, and duration of the sound exposure. In
general, sudden, high level sounds can cause hearing loss, as can
longer exposures to lower level sounds. Temporary or permanent loss of
hearing will occur almost exclusively for noise within an animal's
hearing range. In this section, we first describe specific
manifestations of acoustic effects before providing discussion specific
to the proposed activities in the next section.
Permanent Threshold Shift--Marine mammals exposed to high-intensity
sound, or to lower-intensity sound for prolonged periods, can
experience hearing threshold shift (TS), which is the loss of hearing
sensitivity at certain frequency ranges (Finneran 2015). TS can be
permanent (PTS), in which case the loss of hearing sensitivity is not
fully recoverable, or temporary (TTS), in which case the animal's
hearing threshold would recover over time (Southall et al., 2007).
Repeated sound exposure that leads to TTS could cause PTS. In severe
cases of PTS, there can be total or partial deafness, while in most
cases the animal has an impaired ability to hear sounds in specific
frequency ranges (Kryter 1985).
When PTS occurs, there is physical damage to the sound receptors in
the ear (i.e., tissue damage), whereas TTS represents primarily tissue
fatigue and is reversible (Southall et al., 2007). In addition, other
investigators have suggested that TTS is within the normal bounds of
physiological variability and tolerance and does not represent physical
injury (e.g., Ward, 1997). Therefore, NMFS does not consider TTS to
constitute auditory injury.
Relationships between TTS and PTS thresholds have not been studied
in marine mammals--PTS data exists only for a single harbor seal
(Kastak et al., 2008)--but are assumed to be similar to those in humans
and other terrestrial mammals. PTS typically occurs at exposure levels
at least several decibels above (a 40-dB threshold shift approximates
PTS onset; e.g., Kryter et al., 1966; Miller, 1974) that inducing mild
TTS (a 6-dB threshold shift approximates TTS onset; e.g., Southall et
al., 2007). Based on data from terrestrial mammals, a precautionary
assumption is that the PTS thresholds for impulse sounds (such as
impact pile driving pulses as received close to the source) are at
least six dB higher than the TTS threshold on a peak-pressure basis and
PTS cumulative sound exposure level (SEL) thresholds are 15
[[Page 37251]]
to 20 dB higher than TTS cumulative SEL thresholds (Southall et al.,
2007).
Temporary Threshold Shift--TTS is the mildest form of hearing
impairment that can occur during exposure to sound (Kryter, 1985).
While experiencing TTS, the hearing threshold rises, and a sound must
be at a higher level in order to be heard. In terrestrial and marine
mammals, TTS can last from minutes or hours to days (in cases of strong
TTS). In many cases, hearing sensitivity recovers rapidly after
exposure to the sound ends.
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. 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.
Currently, TTS data only exist for four species of cetaceans
(bottlenose dolphin (Tursiops truncatus), beluga whale, harbor
porpoise, and Yangtze finless porpoise (Neophocoena asiaeorientalis))
and three species of pinnipeds (northern elephant seal (Mirounga
angustirostris), harbor seal, and California sea lion (Zalophus
californianus)) exposed to a limited number of sound sources (i.e.,
mostly tones and octave-band noise) in laboratory settings (Finneran
2015). TTS was not observed in trained spotted and ringed seals exposed
to impulsive noise at levels matching previous predictions of TTS onset
(Reichmuth et al., 2016). In general, harbor seals and harbor porpoises
have a lower TTS onset than other measured pinniped or cetacean
species. Additionally, the existing marine mammal TTS data come from a
limited number of individuals within these species. There are no data
available on noise-induced hearing loss for mysticetes. For summaries
of data on TTS in marine mammals or for further discussion of TTS onset
thresholds, please see Southall et al. (2007), Finneran and Jenkins
(2012), and Finneran (2015).
Behavioral effects--Behavioral disturbance may include a variety of
effects, including subtle changes in behavior (e.g., minor or brief
avoidance of an area or changes in vocalizations), more conspicuous
changes in similar behavioral activities, and more sustained and/or
potentially severe reactions, such as displacement from or abandonment
of high-quality habitat. Behavioral responses to sound are highly
variable and context-specific and any reactions depend on numerous
intrinsic and extrinsic factors (e.g., species, state of maturity,
experience, current activity, reproductive state, auditory sensitivity,
time of day), as well as the interplay between factors (e.g.,
Richardson et al., 1995; Wartzok et al., 2003; Southall et al., 2007;
Weilgart, 2007; Archer et al., 2010). Behavioral reactions can vary not
only among individuals but also within an individual, depending on
previous experience with a sound source, context, and numerous other
factors (Ellison et al., 2012), and can vary depending on
characteristics associated with the sound source (e.g., whether it is
moving or stationary, number of sources, distance from the source).
Please see Appendices B-C of Southall et al. (2007) for a review of
studies involving marine mammal behavioral responses to sound.
Habituation can occur when an animal's response to a stimulus wanes
with repeated exposure, usually in the absence of unpleasant associated
events (Wartzok et al., 2003). Animals are most likely to habituate to
sounds that are predictable and unvarying. It is important to note that
habituation is appropriately considered as a ``progressive reduction in
response to stimuli that are perceived as neither aversive nor
beneficial,'' rather than as, more generally, moderation in response to
human disturbance (Bejder et al., 2009). The opposite process is
sensitization, when an unpleasant experience leads to subsequent
responses, often in the form of avoidance, at a lower level of
exposure. As noted, behavioral state may affect the type of response.
For example, animals that are resting may show greater behavioral
change in response to disturbing sound levels than animals that are
highly motivated to remain in an area for feeding (Richardson et al.
1995; NRC 2003; Wartzok et al. 2003). Controlled experiments with
captive marine mammals have showed pronounced behavioral reactions,
including avoidance of loud sound sources (Ridgway et al. 1997;
Finneran et al. 2003). Observed responses of wild marine mammals to
loud impulsive sound sources (typically seismic airguns or acoustic
harassment devices) have been varied but often consist of avoidance
behavior or other behavioral changes suggesting discomfort (Morton and
Symonds 2002; see also Richardson et al., 1995; Nowacek et al., 2007).
Available studies show wide variation in response to underwater
sound; therefore, it is difficult to predict specifically how any given
sound in a particular instance might affect marine mammals perceiving
the signal. If a marine mammal does react briefly to an underwater
sound by changing its behavior or moving a small distance, the impacts
of the change are unlikely to be significant to the individual, let
alone the stock or population. However, if a sound source displaces
marine mammals from an important feeding or breeding area for a
prolonged period, impacts on individuals and populations could be
significant (e.g., Lusseau and Bejder 2007; Weilgart 2007; NRC 2003).
However, there are broad categories of potential response, which we
describe in greater detail here, that include alteration of dive
behavior, alteration of foraging behavior, effects to breathing,
interference with or alteration of vocalization, avoidance, and flight.
Changes in dive behavior can vary widely, and may consist of
increased or decreased dive times and surface intervals as well as
changes in the rates of ascent and descent during a dive (e.g., Frankel
and Clark 2000; Costa et al., 2003; Ng and Leung, 2003; Nowacek et al.,
2004; Goldbogen et al., 2013). Variations in dive behavior may reflect
interruptions in biologically significant activities (e.g., foraging)
or they may be of little biological significance. The impact of an
alteration to dive behavior resulting from an acoustic exposure depends
on what the animal is doing at the time of the exposure and the type
and magnitude of the response.
Disruption of feeding behavior can be difficult to correlate with
anthropogenic sound exposure, so it is usually inferred by observed
displacement from known foraging areas, the appearance of secondary
indicators (e.g., bubble nets or sediment plumes), or changes in dive
behavior. As for other types of behavioral response, the frequency,
duration, and temporal pattern of signal presentation, as well as
differences in species sensitivity, are likely contributing factors to
differences in response in any given circumstance (e.g., Croll et al.,
2001; Nowacek et al.; 2004; Madsen et al., 2006; Yazvenko et al.,
2007). A determination of whether foraging disruptions incur fitness
consequences would require information on or estimates of the energetic
requirements of the affected
[[Page 37252]]
individuals and the relationship between prey availability, foraging
effort and success, and the life history stage of the animal.
Variations in respiration naturally vary with different behaviors
and alterations to breathing rate as a function of acoustic exposure
can be expected to co-occur with other behavioral reactions, such as a
flight response or an alteration in diving. However, respiration rates
in and of themselves may be representative of annoyance or an acute
stress response. Various studies have shown that respiration rates may
either be unaffected or could increase, depending on the species and
signal characteristics, again highlighting the importance in
understanding species differences in the tolerance of underwater noise
when determining the potential for impacts resulting from anthropogenic
sound exposure (e.g., Kastelein et al., 2001, 2005b, 2006; Gailey et
al., 2007).
Marine mammals vocalize for different purposes and across multiple
modes, such as whistling, echolocation click production, calling, and
singing. Changes in vocalization behavior in response to anthropogenic
noise can occur for any of these modes and may result from a need to
compete with an increase in background noise or may reflect increased
vigilance or a startle response. For example, in the presence of
potentially masking signals, humpback whales and killer whales have
been observed to increase the length of their songs (Miller et al.,
2000; Fristrup et al., 2003; Foote et al., 2004), while right whales
have been observed to shift the frequency content of their calls upward
while reducing the rate of calling in areas of increased anthropogenic
noise (Parks et al., 2007b). In some cases, animals may cease sound
production during production of aversive signals (Bowles et al., 1994).
Avoidance is the displacement of an individual from an area or
migration path as a result of the presence of a sound or other
stressors, and is one of the most obvious manifestations of disturbance
in marine mammals (Richardson et al., 1995). For example, gray whales
are known to change direction--deflecting from customary migratory
paths--in order to avoid noise from seismic surveys (Malme et al.,
1984). Avoidance may be short-term, with animals returning to the area
once the noise has ceased (e.g., Bowles et al., 1994; Goold, 1996;
Morton and Symonds, 2002; Gailey et al., 2007). Longer-term
displacement is possible, however, which may lead to changes in
abundance or distribution patterns of the affected species in the
affected region if habituation to the presence of the sound does not
occur (e.g., Blackwell et al., 2004; Bejder et al., 2006).
A flight response is a dramatic change in normal movement to a
directed and rapid movement away from the perceived location of a sound
source. The flight response differs from other avoidance responses in
the intensity of the response (e.g., directed movement, rate of
travel). Relatively little information on flight responses of marine
mammals to anthropogenic signals exist, although observations of flight
responses to the presence of predators have occurred (Connor and
Heithaus 1996). The result of a flight response could range from brief,
temporary exertion and displacement from the area where the signal
provokes flight to, in extreme cases, marine mammal strandings (Evans
and England 2001). However, it should be noted that response to a
perceived predator does not necessarily invoke flight (Ford and Reeves
2008), and whether individuals are solitary or in groups may influence
the response.
Behavioral disturbance can also impact marine mammals in more
subtle ways. Increased vigilance may result in costs related to
diversion of focus and attention (i.e., when a response consists of
increased vigilance, it may come at the cost of decreased attention to
other critical behaviors such as foraging or resting). These effects
have generally not been demonstrated for marine mammals, but studies
involving fish and terrestrial animals have shown that increased
vigilance may substantially reduce feeding rates (e.g., Beauchamp and
Livoreil,1997; Fritz et al., 2002; Purser and Radford 2011). In
addition, chronic disturbance can cause population declines through
reduction of fitness (e.g., decline in body condition) and subsequent
reduction in reproductive success, survival, or both (e.g., Harrington
and Veitch 1992; Daan et al., 1996; Bradshaw et al., 1998). However,
Ridgway et al. (2006) reported that increased vigilance in bottlenose
dolphins exposed to sound over a five-day period did not cause any
sleep deprivation or stress effects.
Many animals perform vital functions, such as feeding, resting,
traveling, and socializing, on a diel cycle (24-hour cycle). Disruption
of such functions resulting from reactions to stressors such as sound
exposure are more likely to be significant if they last more than one
diel cycle or recur on subsequent days (Southall et al., 2007).
Consequently, a behavioral response lasting less than one day and not
recurring on subsequent days is not considered particularly severe
unless it could directly affect reproduction or survival (Southall et
al., 2007). Note that there is a difference between multi-day
substantive behavioral reactions and multi-day anthropogenic
activities. For example, just because an activity lasts for multiple
days does not necessarily mean that individual animals are either
exposed to activity-related stressors for multiple days or, further,
exposed in a manner resulting in sustained multi-day substantive
behavioral responses.
For non-impulsive sounds (i.e., similar to the sources used during
the proposed action), data suggest that exposures of pinnipeds to
sources between 90 and 140 dB re 1 [mu]Pa do not elicit strong
behavioral responses; no data were available for exposures at higher
received levels for Southall et al. (2007) to include in the severity
scale analysis. Reactions of harbor seals were the only available data
for which the responses could be ranked on the severity scale. For
reactions that were recorded, the majority (17 of 18 individuals/
groups) were ranked on the severity scale as a 4 (defined as moderate
change in movement, brief shift in group distribution, or moderate
change in vocal behavior) or lower; the remaining response was ranked
as a 6 (defined as minor or moderate avoidance of the sound source).
Additional data on hooded seals (Cystophora cristata) indicate
avoidance responses to signals above 160-170 dB re 1 [mu]Pa (Kvadsheim
et al., 2010), and data on grey (Halichoerus grypus) and harbor seals
indicate avoidance response at received levels of 135-144 dB re 1
[mu]Pa (G[ouml]tz et al., 2010). In each instance where food was
available, which provided the seals motivation to remain near the
source, habituation to the signals occurred rapidly. In the same study,
it was noted that habituation was not apparent in wild seals where no
food source was available (G[ouml]tz et al. 2010). This implies that
the motivation of the animal is necessary to consider in determining
the potential for a reaction. In one study aimed to investigate the
under-ice movements and sensory cues associated with under-ice
navigation of ice seals, acoustic transmitters (60-69 kHz at 159 dB re
1 [mu]Pa at 1 m) were attached to ringed seals (Wartzok et al., 1992a;
Wartzok et al., 1992b). An acoustic tracking system then was installed
in the ice to receive the acoustic signals and provide real-time
tracking of ice seal movements. Although the frequencies used in this
study are at the upper limit of ringed seal hearing, the ringed seals
appeared
[[Page 37253]]
unaffected by the acoustic transmissions, as they were able to maintain
normal behaviors (e.g., finding breathing holes).
Seals exposed to non-impulsive sources with a received sound
pressure level within the range of calculated exposures (142-193 dB re
1 [mu]Pa), have been shown to change their behavior by modifying diving
activity and avoidance of the sound source (G[ouml]tz et al., 2010;
Kvadsheim et al., 2010). Although a minor change to a behavior may
occur as a result of exposure to the sources in the proposed action,
these changes would be within the normal range of behaviors for the
animal (e.g., the use of a breathing hole further from the source,
rather than one closer to the source, would be within the normal range
of behavior) (Kelly et al. 1988).
Some behavioral response studies have been conducted on odontocete
responses to sonar. In studies that examined sperm whales (Physeter
macrocephalus) and false killer whales (Pseudorca crassidens) (both in
the mid-frequency cetacean hearing group), the marine mammals showed
temporary cessation of calling and avoidance of sonar sources (Akamatsu
et al., 1993; Watkins and Schevill 1975). Sperm whales resumed calling
and communication approximately two minutes after the pings stopped
(Watkins and Schevill 1975). False killer whales moved away from the
sound source but returned to the area between 0 and 10 minutes after
the end of transmissions (Akamatsu et al., 1993). Many of the
contextual factors resulting from the behavioral response studies
(e.g., close approaches by multiple vessels or tagging) would not occur
during the proposed action. Odontocete behavioral responses to acoustic
transmissions from non-impulsive sources used during the proposed
action would likely be a result of the animal's behavioral state and
prior experience rather than external variables such as ship proximity;
thus, if significant behavioral responses occur they would likely be
short term. In fact, no significant behavioral responses such as panic,
stranding, or other severe reactions have been observed during
monitoring of actual training exercises (Department of the Navy 2011,
2014; Smultea and Mobley 2009; Watwood et al., 2012).
Icebreaking noise has the potential to disturb marine mammals and
elicit an alerting, avoidance, or other behavioral reaction (Huntington
et al., 2015; Pirotta et al., 2015; Williams et al., 2014). Icebreaking
in fast ice during the spring can cause behavioral reactions in beluga
whales. However, icebreaking associated with the proposed action would
only occur from August through October, which lessens the probability
of a whale encountering the vessel (in comparison to other sources in
the proposed action that would be active year-round).
Ringed seals and bearded seals on pack ice showed various behaviors
when approached by an icebreaking vessel. A majority of seals dove
underwater when the ship was within 0.5 nautical miles (0.93 km) while
others remained on the ice. However, as icebreaking vessels came closer
to the seals, most dove underwater. Ringed seals have also been
observed foraging in the wake of an icebreaking vessel (Richardson et
al., 1995). In studies by Alliston (1980; 1981), there was no observed
change in the density of ringed seals in areas that had been subject to
icebreaking. Alternatively, ringed seals may have preferentially
established breathing holes in the ship tracks after the icebreaker
moved through the area. Due to the time of year of the activity (August
through October), ringed seals are not expected to be within the
subnivean lairs nor pupping (Chapskii 1940; McLaren 1958; Smith and
Stirling 1975).
Adult ringed seals spend up to 20 percent of the time in subnivean
lairs during the winter season (Kelly et al., 2010a). Ringed seal pups
spend about 50 percent of their time in the lair during the nursing
period (Lydersen and Hammill 1993). During the warm season both bearded
seals and ringed seals haul out on the ice. In a study of ringed seal
haulout activity by Born et al. (2002), ringed seals spent 25-57
percent of their time hauled out in June which is during their molting
season. Bearded seals also spend a large amount of time hauled out
during the molting season between April and August (Reeves et al.,
2002). Ringed seal lairs are typically used by individual seals
(haulout lairs) or by a mother with a pup (birthing lairs); large lairs
used by many seals for hauling out are rare (Smith and Stirling 1975).
If the non-impulsive acoustic transmissions are heard and are perceived
as a threat, ringed seals within subnivean lairs could react to the
sound in a similar fashion to their reaction to other threats, such as
polar bears (their primary predators), although the type of sound would
be novel to them. Responses of ringed seals to a variety of human-
induced sounds (e.g., helicopter noise, snowmobiles, dogs, people, and
seismic activity) have been variable; some seals entered the water and
some seals remained in the lair. However, in all instances in which
observed seals departed lairs in response to noise disturbance, they
subsequently reoccupied the lair (Kelly et al., 1988).
Ringed seal mothers have a strong bond with their pups and may
physically move their pups from the birth lair to an alternate lair to
avoid predation, sometimes risking their lives to defend their pups
from potential predators (Smith 1987). If a ringed seal mother
perceives the proposed acoustic sources as a threat, the network of
multiple birth and haulout lairs allows the mother and pup to move to a
new lair (Smith and Hammill 1981; Smith and Stirling 1975). The
acoustic sources and icebreaking noise from this proposed action are
not likely to impede a ringed seal from finding a breathing hole or
lair, as captive seals have been found to primarily use vision to
locate breathing holes and no effect to ringed seal vision would occur
from the acoustic disturbance (Elsner et al., 1989; Wartzok et al.,
1992a). It is anticipated that a ringed seal would be able to relocate
to a different breathing hole relatively easily without impacting their
normal behavior patterns.
Stress responses--An animal's perception of a threat may be
sufficient to trigger stress responses consisting of some combination
of behavioral responses, autonomic nervous system responses,
neuroendocrine responses, or immune responses (e.g., Seyle 1950; Moberg
2000). In many cases, an animal's first and sometimes most economical
(in terms of energetic costs) response is behavioral avoidance of the
potential stressor. Autonomic nervous system responses to stress
typically involve changes in heart rate, blood pressure, and
gastrointestinal activity. These responses have a relatively short
duration and may or may not have a significant long-term effect on an
animal's fitness.
Neuroendocrine stress responses often involve the hypothalamus-
pituitary-adrenal 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, altered metabolism, reduced immune
competence, and behavioral disturbance (e.g., Moberg, 1987; Blecha,
2000). Increases in the circulation of glucocorticoids are also equated
with stress (Romano et al., 2004).
The primary distinction between stress (which is adaptive and does
not normally place an animal at risk) and ``distress'' is the cost of
the response. During a stress response, an animal uses glycogen stores
that can be quickly
[[Page 37254]]
replenished once the stress is alleviated. In such circumstances, the
cost of the stress response would not pose serious fitness
consequences. 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 functions. This state of distress
will last until the animal replenishes its energetic reserves
sufficient to restore normal function.
Relationships between these physiological mechanisms, animal
behavior, and the costs of stress responses are well-studied through
controlled experiments and for both laboratory and free-ranging animals
(e.g., Holberton et al., 1996; Hood et al., 1998; Jessop et al., 2003;
Krausman et al., 2004; Lankford et al., 2005). Stress responses due to
exposure to anthropogenic sounds or other stressors and their effects
on marine mammals have also been reviewed (Fair and Becker, 2000;
Romano et al., 2002b) and, more rarely, studied in wild populations
(e.g., Romano et al., 2002a). These and other studies lead to a
reasonable expectation that some marine mammals will experience
physiological stress responses upon exposure to acoustic stressors and
that it is possible that some of these would be classified as
``distress.'' In addition, any animal experiencing TTS would likely
also experience stress responses (NRC, 2003).
Auditory masking--Sound can disrupt behavior through masking, or
interfering with, an animal's ability to detect, recognize, or
discriminate between acoustic signals of interest (e.g., those used for
intraspecific communication and social interactions, prey detection,
predator avoidance, navigation) (Richardson et al., 1995). Masking
occurs when the receipt of a sound is interfered with by another
coincident sound at similar frequencies and at similar or higher
intensity, and may occur whether the sound is natural (e.g., snapping
shrimp, wind, waves, precipitation) or anthropogenic (e.g., shipping,
sonar, seismic exploration) in origin. The ability of a noise source to
mask biologically important sounds depends on the characteristics of
both the noise source and the signal of interest (e.g., signal-to-noise
ratio, temporal variability, direction), in relation to each other and
to an animal's hearing abilities (e.g., sensitivity, frequency range,
critical ratios, frequency discrimination, directional discrimination,
age or TTS hearing loss), and existing ambient noise and propagation
conditions.
Under certain circumstances, marine mammals experiencing
significant masking could also be impaired from maximizing their
performance fitness in survival and reproduction. Therefore, when the
coincident (masking) sound is anthropogenic, it may be considered
harassment when disrupting or altering critical behaviors. It is
important to distinguish TTS and PTS, which persist after the sound
exposure, from masking, which occurs during the sound exposure. Because
masking (without resulting in TS) is not associated with abnormal
physiological function, it is not considered a physiological effect,
but rather a potential behavioral effect.
The frequency range of the potentially masking sound is important
in determining any potential behavioral impacts. For example, low-
frequency signals may have less effect on high-frequency echolocation
sounds produced by odontocetes but are more likely to affect detection
of mysticete communication calls and other potentially important
natural sounds such as those produced by surf and some prey species.
The masking of communication signals by anthropogenic noise may be
considered as a reduction in the communication space of animals (e.g.,
Clark et al., 2009) and may result in energetic or other costs as
animals change their vocalization behavior (e.g., Miller et al., 2000;
Foote et al., 2004; Parks et al., 2007b; Di Iorio and Clark, 2009; Holt
et al., 2009). Masking can be reduced in situations where the signal
and noise come from different directions (Richardson et al., 1995),
through amplitude modulation of the signal, or through other
compensatory behaviors (Houser and Moore, 2014). Masking can be tested
directly in captive species (e.g., Erbe, 2008), but in wild populations
it must be either modeled or inferred from evidence of masking
compensation. There are few studies addressing real-world masking
sounds likely to be experienced by marine mammals in the wild (e.g.,
Branstetter et al., 2013).
Masking affects both senders and receivers of acoustic signals and
can potentially have long-term chronic effects on marine mammals at the
population level as well as at the individual level. Low-frequency
ambient sound levels have increased by as much as 20 dB (more than
three times in terms of SPL) in the world's ocean from pre-industrial
periods, with most of the increase from distant commercial shipping
(Hildebrand 2009). All anthropogenic sound sources, but especially
chronic and lower-frequency signals (e.g., from vessel traffic),
contribute to elevated ambient sound levels, thus intensifying masking.
Potential Effects on Prey--The marine mammal species in the study
area feed on marine invertebrates and fish. Studies of sound energy
effects on invertebrates are few, and primarily identify behavioral
responses. It is expected that most marine invertebrates would not
sense the frequencies of the acoustic transmissions from the acoustic
sources associated with the proposed action. Although acoustic sources
used during the proposed action may briefly impact individuals,
intermittent exposures to non-impulsive acoustic sources are not
expected to impact survival, growth, recruitment, or reproduction of
widespread marine invertebrate populations. Impacts to invertebrates
from icebreaking noise is unknown, but it is likely that some species
including crustaceans and cephalopods would be able to perceive the low
frequency sounds generated from icebreaking. Icebreaking associated
with the proposed action would be short-term and temporary as the
vessel moves through an area, and it is not anticipated that this
short-term noise would result in significant harm, nor is it expected
to result in more than a temporary behavioral reaction of marine
invertebrates in the vicinity of the icebreaking event.
The fish species residing in the study area include those that are
closely associated with the deep ocean habitat of the Beaufort Sea.
Nearly 250 marine fish species have been described in the Arctic,
excluding the larger parts of the sub-Arctic Bering, Barents, and
Norwegian Seas (Mecklenburg et al., 2011). However, only about 30 are
known to occur in the Arctic waters of the Beaufort Sea (Christiansen
and Reist 2013). Although hearing capability data only exist for fewer
than 100 of the 32,000 named fish species, current data suggest that
most species of fish detect sounds from 50 to 100 Hz, with few fish
hearing sounds above 4 kHz (Popper 2008). It is believed that most fish
have the best hearing sensitivity from 100 to 400 Hz (Popper 2003).
Fish species in the study area are expected to hear the low-frequency
sources associated with the proposed action, but most are not expected
to detect sound from the mid-frequency sources. Human generated sound
could alter the behavior of a fish in a manner than would affect its
way of living, such as where it tries to locate food or how well it
could find a mate. Behavioral responses to loud noise could include a
startle response, such as the fish swimming away from the source, the
fish ``freezing'' and staying in place, or scattering (Popper 2003).
[[Page 37255]]
Icebreaking noise has the potential to expose fish to both sound and
general disturbance, which could result in short-term behavioral or
physiological responses (e.g., avoidance, stress, increased heart
rate). Misund (1997) found that fish ahead of a ship showed avoidance
reactions at ranges of 160 to 489 ft (49 to 149 m). Avoidance behavior
of vessels, vertically or horizontally in the water column, has been
reported for cod and herring, and was attributed to vessel noise. While
acoustic sources and icebreaking associated with the proposed action
may influence the behavior of some fish species, other fish species may
be equally unresponsive. Overall effects to fish from the proposed
action would be localized, temporary, and infrequent.
Effects to Physical and Foraging Habitat--Icebreaking activities
include the physical pushing or moving of ice to allow vessels to
proceed through ice-covered waters. Breaking of pack ice that contains
hauled out seals may result in the animals becoming startled and
entering the water, but such effects would be brief. Bearded and ringed
seals haul out on pack ice during the spring and summer to molt (Reeves
et al. 2002; Born et al., 2002). Due to the time of year of the
icebreaking activity (August through October), ringed seals are not
expected to be within the subnivean lairs nor pupping (Chapskii 1940;
McLaren 1958; Smith and Stirling 1975). Additionally, studies by
Alliston (Alliston 1980; Alliston 1981) suggested that ringed seals may
preferentially establish breathing holes in ship tracks after
icebreakers move through the area. The amount of ice habitat disturbed
by icebreaking activities is small relative to the amount of overall
habitat available. There will be no permanent loss or modification of
physical ice habitat used by bearded or ringed seals. Icebreaking would
have no effect on physical beluga habitat as beluga habitat is solely
within the water column.
Testing of towed sources and icebreaking noise would be limited in
duration and the deployed sources that would remain in use after the
vessels have left the survey area have low duty cycles and lower source
levels. There would not be any expected habitat-related effects from
non-impulsive acoustic sources or icebreaking noise that could impact
the in-water habitat of ringed seal, bearded seal, or beluga whale
foraging habitat.
Estimated Take
This section provides an estimate of the number of incidental takes
proposed for authorization through this IHA, which will inform both
NMFS' consideration of ``small numbers'' and the negligible impact
determination.
Harassment is the only type of take expected to result from these
activities. For this military readiness activity, the MMPA defines
``harassment'' as (i) Any act that injures or has the significant
potential to injure a marine mammal or marine mammal stock in the wild
(Level A harassment); or (ii) Any act that disturbs or is likely to
disturb a marine mammal or marine mammal stock in the wild by causing
disruption of natural behavioral patterns, including, but not limited
to, migration, surfacing, nursing, breeding, feeding, or sheltering, to
a point where such behavioral patterns are abandoned or significantly
altered (Level B harassment).
Authorized takes would be by Level B harassment only, in the form
of disruption of behavioral patterns and TTS for individual marine
mammals resulting from exposure to acoustic transmissions and
icebreaking noise. Based on the nature of the activity, Level A
harassment is neither anticipated nor proposed to be authorized.
As described previously, no mortality is anticipated or proposed to
be authorized for this activity. Below we describe how the take is
estimated.
Generally speaking, we estimate take by considering: (1) Acoustic
thresholds above which NMFS believes the best available science
indicates marine mammals will be behaviorally harassed or incur some
degree of permanent hearing impairment; (2) the area or volume of water
that will be ensonified above these levels in a day; (3) the density or
occurrence of marine mammals within these ensonified areas; and, (4)
and the number of days of activities. We note that while these basic
factors can contribute to a basic calculation to provide an initial
prediction of takes, additional information that can qualitatively
inform take estimates is also sometimes available (e.g., previous
monitoring results or average group size). For the proposed IHA, ONR
employed a sophisticated model known as the Navy Acoustic Effects Model
(NAEMO) for assessing the impacts of underwater sound. Below, we
describe the factors considered here in more detail and present the
proposed take estimate.
Acoustic Thresholds
Using the best available science, NMFS has developed acoustic
thresholds that identify the received level of underwater sound above
which exposed marine mammals would be reasonably expected to be
behaviorally harassed (equated to Level B harassment) or to incur PTS
of some degree (equated to Level A harassment).
Level B Harassment for non-explosive sources--In coordination with
NMFS, the Navy developed behavioral thresholds to support environmental
analyses for the Navy's testing and training military readiness
activities utilizing active sonar sources; these behavioral harassment
thresholds are used here to evaluate the potential effects of the
active sonar components of the proposed action. The response of a
marine mammal to an anthropogenic sound will depend on the frequency,
duration, temporal pattern and amplitude of the sound as well as the
animal's prior experience with the sound and the context in which the
sound is encountered (i.e., what the animal is doing at the time of the
exposure). The distance from the sound source and whether it is
perceived as approaching or moving away can also affect the way an
animal responds to a sound (Wartzok et al. 2003). For marine mammals, a
review of responses to anthropogenic sound was first conducted by
Richardson et al. (1995). Reviews by Nowacek et al. (2007) and Southall
et al. (2007) address studies conducted since 1995 and focus on
observations where the received sound level of the exposed marine
mammal(s) was known or could be estimated.
Multi-year research efforts have conducted sonar exposure studies
for odontocetes and mysticetes (Miller et al. 2012; Sivle et al. 2012).
Several studies with captive animals have provided data under
controlled circumstances for odontocetes and pinnipeds (Houser et al.
2013a; Houser et al. 2013b). Moretti et al. (2014) published a beaked
whale dose-response curve based on passive acoustic monitoring of
beaked whales during U.S. Navy training activity at Atlantic Underwater
Test and Evaluation Center during actual Anti-Submarine Warfare
exercises. This new information necessitated the update of the
behavioral response criteria for the U.S. Navy's environmental
analyses.
Southall et al. (2007), and more recently Southall et al. (2019),
synthesized data from many past behavioral studies and observations to
determine the likelihood of behavioral reactions at specific sound
levels. While in general, the louder the sound source the more intense
the behavioral response, it was clear that the proximity of a sound
source and the animal's experience, motivation, and conditioning were
also critical factors influencing the response (Southall et al. 2007;
Southall et al. 2019). After examining all of the available data, the
authors felt that the derivation of
[[Page 37256]]
thresholds for behavioral response based solely on exposure level was
not supported because context of the animal at the time of sound
exposure was an important factor in estimating response. Nonetheless,
in some conditions, consistent avoidance reactions were noted at higher
sound levels depending on the marine mammal species or group allowing
conclusions to be drawn. Phocid seals showed avoidance reactions at or
below 190 dB re 1 [mu]Pa at 1m; thus, seals may actually receive levels
adequate to produce TTS before avoiding the source.
Odontocete behavioral criteria for non-impulsive sources were
updated based on controlled exposure studies for dolphins and sea
mammals, sonar, and safety (3S) studies where odontocete behavioral
responses were reported after exposure to sonar (Antunes et al., 2014;
Houser et al., 2013b); Miller et al., 2011; Miller et al., 2014; Miller
et al., 2012). For the 3S study the sonar outputs included 1-2 kHz up-
and down-sweeps and 6-7 kHz up-sweeps; source levels were ramped up
from 152-158 dB re 1 [micro]Pa to a maximum of 198-214 re 1 [micro]Pa
at 1 m. Sonar signals were ramped up over several pings while the
vessel approached the mammals. The study did include some control
passes of ships with the sonar off to discern the behavioral responses
of the mammals to vessel presence alone versus active sonar.
The controlled exposure studies included exposing the Navy's
trained bottlenose dolphins to mid-frequency sonar while they were in a
pen. Mid-frequency sonar was played at 6 different exposure levels from
125-185 dB re 1 [micro]Pa (rms). The behavioral response function for
odontocetes resulting from the studies described above has a 50 percent
probability of response at 157 dB re 1 [micro]Pa. Additionally,
distance cutoffs (20 km for MF cetaceans) were applied to exclude
exposures beyond which the potential of significant behavioral
responses is considered to be unlikely.
The pinniped behavioral threshold was updated based on controlled
exposure experiments on the following captive animals: Hooded seal,
gray seal, and California sea lion (G[ouml]tz et al. 2010; Houser et
al. 2013a; Kvadsheim et al. 2010). Hooded seals were exposed to
increasing levels of sonar until an avoidance response was observed,
while the grey seals were exposed first to a single received level
multiple times, then an increasing received level. Each individual
California sea lion was exposed to the same received level ten times.
These exposure sessions were combined into a single response value,
with an overall response assumed if an animal responded in any single
session. The resulting behavioral response function for pinnipeds has a
50 percent probability of response at 166 dB re 1 [mu]Pa. Additionally,
distance cutoffs (10 km for pinnipeds) were applied to exclude
exposures beyond which the potential of significant behavioral
responses is considered to be unlikely.
NMFS is proposing to adopt the Navy's approach to estimating
incidental take by Level B harassment from the active acoustic sources
for this action, which includes use of these dose response functions.
The Navy's dose response functions were developed to estimate take from
sonar and similar transducers and are not applicable to icebreaking.
NMFS predicts that marine mammals are likely to be behaviorally
harassed in a manner we consider Level B harassment when exposed to
underwater anthropogenic noise above received levels of 120 dB re 1
[mu]Pa (rms) for continuous (e.g., vibratory pile-driving, drilling,
icebreaking) and above 160 dB re 1 [mu]Pa (rms) for non-explosive
impulsive (e.g., seismic airguns) or intermittent (e.g., scientific
sonar) sources. Thus, take of marine mammals by Level B harassment due
to icebreaking has been calculated using the Navy's NAEMO model with a
step-function at 120 dB re 1 [micro]Pa (rms) received level for
behavioral response.
Level A harassment for non-explosive sources--NMFS' Technical
Guidance for Assessing the Effects of Anthropogenic Sound on Marine
Mammal Hearing (Version 2.0) (Technical Guidance, 2018) identifies dual
criteria to assess auditory injury (Level A harassment) to five
different marine mammal groups (based on hearing sensitivity) as a
result of exposure to noise from two different types of sources
(impulsive or non-impulsive). ONR's proposed activities involve only
non-impulsive sources.
These thresholds are provided in the table below. The references,
analysis, and methodology used in the development of the thresholds are
described in NMFS 2018 Technical Guidance, which may be accessed at
https://www.fisheries.noaa.gov/national/marine-mammal-protection/marine-mammal-acoustic-technical-guidance.
Table 5--Thresholds Identifying the Onset of Permanent Threshold Shift
----------------------------------------------------------------------------------------------------------------
PTS onset acoustic thresholds \*\ (received level)
Hearing Group ------------------------------------------------------------------------
Impulsive Non-impulsive
----------------------------------------------------------------------------------------------------------------
Low-Frequency (LF) Cetaceans........... Cell 1: Lpk,flat: 219 dB: Cell 2: LE,LF,24h: 199 dB.
LE,LF,24h: 183 dB.
Mid-Frequency (MF) Cetaceans........... Cell 3: Lpk,flat: 230 dB; Cell 4: LE,MF,24h: 198 dB.
LE,MF,24h: 185 dB.
High-Frequency (HF) Cetaceans.......... Cell 5: Lpk,flat: 202 dB; Cell 6 LE,HF,24h: 173 dB.
LE,HF,24h: 155 dB.
Phocid Pinnipeds (PW).................. Cell 7: Lpk,flat: 218 dB; Cell 8: LE,PW,24h: 201 dB.
(Underwater)........................... LE,PW,24h: 185 dB..
Otariid Pinnipeds (OW)................. Cell 9: Lpk,flat: 232 dB; Cell 10: LE,OW,24h: 219 dB.
(Underwater)........................... LE,OW,24h: 203 dB..
----------------------------------------------------------------------------------------------------------------
* Dual metric acoustic thresholds for impulsive sounds: Use whichever results in the largest isopleth for
calculating PTS onset. If a non-impulsive sound has the potential of exceeding the peak sound pressure level
thresholds associated with impulsive sounds, these thresholds should also be considered.
Note:--Peak sound pressure (Lpk) has a reference value of 1 [micro]Pa, and cumulative sound exposure level (LE)
has a reference value of 1[micro]Pa\2\s. In this Table, thresholds are abbreviated to reflect American
National Standards Institute standards (ANSI 2013). However, peak sound pressure is defined by ANSI as
incorporating frequency weighting, which is not the intent for this Technical Guidance. Hence, the subscript
``flat'' is being included to indicate peak sound pressure should be flat weighted or unweighted within the
generalized hearing range. The subscript associated with cumulative sound exposure level thresholds indicates
the designated marine mammal auditory weighting function (LF, MF, and HF cetaceans, and PW and OW pinnipeds)
and that the recommended accumulation period is 24 hours. The cumulative sound exposure level thresholds could
be exceeded in a multitude of ways (i.e., varying exposure levels and durations, duty cycle). When possible,
it is valuable for action proponents to indicate the conditions under which these acoustic thresholds will be
exceeded.
[[Page 37257]]
Quantitative Modeling
The Navy performed a quantitative analysis to estimate the number
of mammals that could be harassed by the underwater acoustic
transmissions during the proposed action. Inputs to the quantitative
analysis included marine mammal density estimates, marine mammal depth
occurrence distributions (Navy 2017a), oceanographic and environmental
data, marine mammal hearing data, and criteria and thresholds for
levels of potential effects. The quantitative analysis consists of
computer modeled estimates and a post-model analysis to determine the
number of potential animal exposures. The model calculates sound energy
propagation from the proposed non-impulsive acoustic sources and
icebreaking, the sound received by animat (virtual animal) dosimeters
representing marine mammals distributed in the area around the modeled
activity, and whether the sound received by animats exceeds the
thresholds for effects.
The Navy developed a set of software tools and compiled data for
estimating acoustic effects on marine mammals without consideration of
behavioral avoidance or mitigation. These tools and data sets serve as
integral components of NAEMO. In NAEMO, animats are distributed non-
uniformly based on species-specific density, depth distribution, and
group size information and animats record energy received at their
location in the water column. A fully three-dimensional environment is
used for calculating sound propagation and animat exposure in NAEMO.
Site-specific bathymetry, sound speed profiles, wind speed, and bottom
properties are incorporated into the propagation modeling process.
NAEMO calculates the likely propagation for various levels of energy
(sound or pressure) resulting from each source used during the training
event.
NAEMO then records the energy received by each animat within the
energy footprint of the event and calculates the number of animats
having received levels of energy exposures that fall within defined
impact thresholds. Predicted effects on the animats within a scenario
are then tallied and the highest order effect (based on severity of
criteria; e.g., PTS over TTS) predicted for a given animat is assumed.
Each scenario, or each 24-hour period for scenarios lasting greater
than 24 hours (which NMFS recommends in order to ensure more consistent
quantification of take across actions), is independent of all others,
and therefore, the same individual marine animal (as represented by an
animat in the model environment) could be impacted during each
independent scenario or 24-hour period. In few instances, although the
activities themselves all occur within the study area, sound may
propagate beyond the boundary of the study area. Any exposures
occurring outside the boundary of the study area are counted as if they
occurred within the study area boundary. NAEMO provides the initial
estimated impacts on marine species with a static horizontal
distribution (i.e., animats in the model environment do not move
horizontally).
There are limitations to the data used in the acoustic effects
model, and the results must be interpreted within this context. While
the best available data and appropriate input assumptions have been
used in the modeling, when there is a lack of definitive data to
support an aspect of the modeling, conservative modeling assumptions
have been chosen (i.e., assumptions that may result in an overestimate
of acoustic exposures):
Animats are modeled as being underwater, stationary, and
facing the source and therefore always predicted to receive the maximum
potential sound level at a given location (i.e., no porpoising or
pinnipeds' heads above water);
Animats do not move horizontally (but change their
position vertically within the water column), which may overestimate
physiological effects such as hearing loss, especially for slow moving
or stationary sound sources in the model;
Animats are stationary horizontally and therefore do not
avoid the sound source, unlike in the wild where animals would most
often avoid exposures at higher sound levels, especially those
exposures that may result in PTS;
Multiple exposures within any 24-hour period are
considered one continuous exposure for the purposes of calculating
potential threshold shift, because there are not sufficient data to
estimate a hearing recovery function for the time between exposures;
and
Mitigation measures were not considered in the model. In
reality, sound-producing activities would be reduced, stopped, or
delayed if marine mammals are detected by visual monitoring.
Because of these inherent model limitations and simplifications,
model-estimated results should be further analyzed, considering such
factors as the range to specific effects, avoidance, and the likelihood
of successfully implementing mitigation measures. This analysis uses a
number of factors in addition to the acoustic model results to predict
acoustic effects on marine mammals.
The underwater radiated noise signature for icebreaking in the
central Arctic Ocean by CGC HEALY during different types of ice-cover
was characterized in Roth et al. (2013). The radiated noise signatures
were characterized for various fractions of ice cover. For modeling,
the 8/10 ice cover was used. Each modeled day of icebreaking consisted
of 6 hours of 8/10 ice cover. Icebreaking was modeled for eight days
for each of the 2019 and 2020 cruises. For each cruise, this includes
four days of icebreaking for the deployment (or recovery) of the VLF
source and four days of icebreaking for the deployment (or recovery) of
the northernmost navigation sources. Since ice forecasting cannot be
predicted more than a few weeks in advance it is unknown if icebreaking
would be needed to deploy or retrieve the sources after one year of
transmitting. Therefore, icebreaking was conservatively analyzed within
this IHA. Figure 5a and 5b in Roth et al. (2013) depicts the source
spectrum level versus frequency for 8/10 ice cover. The sound signature
of the ice coverage level was broken into 1-octave bins (Table 6). In
the model, each bin was included as a separate source on the modeled
vessel. When these independent sources go active concurrently, they
simulate the sound signature of CGC HEALY. The modeled source level
summed across these bins was 196.2 dB for the 8/10 signature ice
signature. These source levels are a good approximation of the
icebreaker's observed source level (provided in Figure 4b of (Roth et
al. 2013)). Each frequency and source level was modeled as an
independent source, and applied simultaneously to all of the animats
within NAEMO. Each second was summed across frequency to estimate sound
pressure level (root mean square (SPLRMS)). For PTS and TTS
determinations, sound exposure levels were summed over the duration of
the test and the transit to the deployment area. The method of
quantitative modeling for icebreaking is considered to be a
conservative approach; therefore, the number of takes estimated for
icebreaking are likely an over-estimate and would not be expected.
Table 6--Modeled Bins for Icebreaking in 8/10 Ice Coverage on CGC HEALY
------------------------------------------------------------------------
Source
Frequency (Hz) level (dB)
------------------------------------------------------------------------
25......................................................... 189
[[Page 37258]]
50......................................................... 188
100........................................................ 189
200........................................................ 190
400........................................................ 188
800........................................................ 183
1600....................................................... 177
3200....................................................... 176
6400....................................................... 172
12800...................................................... 167
------------------------------------------------------------------------
For the other non-impulsive sources, NAEMO calculates the SPL and
SEL for each active emission during an event. This is done by taking
the following factors into account over the propagation paths:
Bathymetric relief and bottom types, sound speed, and attenuation
contributors such as absorption, bottom loss, and surface loss.
Platforms such as a ship using one or more sound sources are modeled in
accordance with relevant vehicle dynamics and time durations by moving
them across an area whose size is representative of the testing event's
operational area. Table 7 provides range to effects for non-impulsive
sources and icebreaking noise proposed for the Arctic research
activities to mid-frequency cetacean and pinniped specific criteria.
Marine mammals within these ranges would be predicted to receive the
associated effect. Range to effects is important information in not
only predicting non-impulsive acoustic impacts, but also in verifying
the accuracy of model results against real-world situations and
determining adequate mitigation ranges to avoid higher level effects,
especially physiological effects in marine mammals. Therefore, the
ranges in Table 7 provide realistic maximum distances over which the
specific effects from the use of non-impulsive sources during the
proposed action would be possible.
Table 7--Range to PTS, TTS, and Behavioral Effects in the Study Area
--------------------------------------------------------------------------------------------------------------------------------------------------------
Range to behavioral effects Range to TTS effects (m) Range to PTS effects (m)
(m) ---------------------------------------------------------------
Source --------------------------------
Piniped MF Piniped MF Piniped
MF cetacean cetacean cetacean
--------------------------------------------------------------------------------------------------------------------------------------------------------
Navigation and real-time sensing sources................ 20,000 \a\ 10,000 \a\ 0 6 0 0
Spiral Wave Beacon source............................... 20,000 \a\ 10,000 \a\ 0 0 0 0
Icebreaking noise....................................... 4,275 4,525 3 12 0 0
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\ Cutoff distances applied.
A behavioral response study conducted on and around the Navy range
in Southern California (SOCAL BRS) observed reactions to sonar and
similar sound sources by several marine mammal species, including
Risso's dolphins (Grampus griseus), a mid-frequency cetacean (DeRuiter
et al., 2013; Goldbogen et al., 2013; Southall et al., 2011; Southall
et al., 2012; Southall et al., 2013; Southall et al., 2014). In
preliminary analysis, none of the Risso's dolphins exposed to simulated
or real mid-frequency sonar demonstrated any overt or obvious responses
(Southall et al., 2012, Southall et al., 2013). In general, although
the responses to the simulated sonar were varied across individuals and
species, none of the animals exposed to real Navy sonar responded;
these exposures occurred at distances beyond 10 km, and were up to 100
km away (DeRuiter et al., 2013; B. Southall pers. comm.). These data
suggest that most odontocetes (not including beaked whales and harbor
porpoises) likely do not exhibit significant behavioral reactions to
sonar and other transducers beyond approximately 10 km. Therefore, the
Navy uses a cutoff distance for odontocetes of 10 km for moderate
source level, single platform training and testing events, and 20 km
for all other events, including the proposed Arctic Research Activities
(Navy 2017a).
Southall et al., (2007) report that pinnipeds do not exhibit strong
reactions to SPLs up to 140 dB re 1 [micro]Pa from non-impulsive
sources. While there are limited data on pinniped behavioral responses
beyond about 3 km in the water, the Navy uses a distance cutoff of 5 km
for moderate source level, single platform training and testing events,
and 10 km for all other events, including the proposed Arctic Research
Activities (Navy 2017a).
NMFS and the Navy conservatively propose a distance cutoff of 10 km
for pinnipeds, and 20 km for mid-frequency cetaceans (Navy 2017a).
Regardless of the received level at that distance, take is not
estimated to occur beyond 10 and 20 km from the source for pinnipeds
and cetaceans, respectively. Sources that show a range of zero do not
rise to the specified level of effects (i.e., there is no chance of PTS
for either MF cetaceans or pinnipeds from any of the sources). No
instances of PTS were modeled for any species or stock; as such, no
take by Level A harassment is anticipated or proposed to be authorized.
As discussed above, within NAEMO animats do not move horizontally
or react in any way to avoid sound. Furthermore, mitigation measures
that reduce the likelihood of physiological impacts are not considered
in quantitative analysis. Therefore, the model may overestimate
acoustic impacts, especially physiological impacts near the sound
source. The behavioral criteria used as a part of this analysis
acknowledges that a behavioral reaction is likely to occur at levels
below those required to cause hearing loss. At close ranges and high
sound levels approaching those that could cause PTS, avoidance of the
area immediately around the sound source is the assumed behavioral
response for most cases.
In previous environmental analyses, the Navy has implemented
analytical factors to account for avoidance behavior and the
implementation of mitigation measures. The application of avoidance and
mitigation factors has only been applied to model-estimated PTS
exposures given the short distance over which PTS is estimated. Given
that no PTS exposures were estimated during the modeling process for
this proposed action, the quantitative consideration of avoidance and
mitigation factors were not included in this analysis.
The marine mammal density numbers utilized for quantitative
modeling are from the Navy Marine Species Density Database (Navy 2014).
Density estimates are based on habitat-based modeling by Kaschner et
al., (2006) and Kaschner (2004). While density estimates for the two
stocks of beluga whales are equal (Kaschner et al., 2006; Kaschner
2004), take has been apportioned to each stock
[[Page 37259]]
proportional to the abundance of each stock. Table 8 shows the
exposures expected for the beluga whale, bearded seal, and ringed seal
based on NAEMO modeled results.
Table 8--Quantitative Modeling Results of Potential Exposures
--------------------------------------------------------------------------------------------------------------------------------------------------------
Density
estimate Level B Level B
within study harassment harassment Level A Total proposed Percentage of
Species area (animals from deployed from harassment take stock taken
per square km) sources icebreaking
\a\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Beluga Whale (Beaufort Sea Stock)....................... 0.0087 331 32 0 363 0.92
Beluga Whale (Eastern Chukchi Sea stock)................ 0.0087 178 18 0 196 0.94
Bearded Seal............................................ 0.0332 0 0 0 \b\ 5 <0.01
Ringed Seal............................................. 0.3760 6,773 1,072 0 7,845 2.17
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\ Kaschner et al. (2006); Kaschner (2004)
\b\ Quantitative modeling yielded zero takes of bearded seals. However, in an abundance of caution, we are proposing to authorize five takes of bearded
seals by Level B harassment.
Effects of Specified Activities on Subsistence Uses of Marine Mammals
Subsistence hunting is important for many Alaska Native
communities. A study of the North Slope villages of Nuiqsut, Kaktovik,
and Barrow identified the primary resources used for subsistence and
the locations for harvest (Stephen R. Braund & Associates 2010),
including terrestrial mammals (caribou, moose, wolf, and wolverine),
birds (geese and eider), fish (Arctic cisco, Arctic char/Dolly Varden
trout, and broad whitefish), and marine mammals (bowhead whale, ringed
seal, bearded seal, and walrus). Bearded seals, ringed seals, and
beluga whales are located within the study area during the proposed
action. The permitted sources would be placed outside of the range for
subsistence hunting and the study plans have been communicated to the
Native communities. The closest active acoustic source within the study
area (aside from the de minimis sources), is approximately 145 mi (233
km) from land. As stated above, the range to effects for non-impulsive
acoustic sources in this experiment is much smaller than the distance
from shore. In addition, the proposed action would not remove
individuals from the population. Therefore, there would be no impacts
caused by this action to the availability of bearded seal, ringed seal,
or beluga whale for subsistence hunting. Therefore, subsistence uses of
marine mammals are not expected to be impacted by the proposed action.
Proposed Mitigation
In order to issue an IHA 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. NMFS regulations require applicants for incidental
take authorizations to include information about the availability and
feasibility (economic and technological) of equipment, methods, and
manner of conducting such activity or other means of effecting the
least practicable adverse impact upon the affected species or stocks
and their habitat (50 CFR 216.104(a)(11)). The NDAA for FY 2004 amended
the MMPA as it relates to military readiness activities and the
incidental take authorization process such that ``least practicable
impact'' shall include consideration of personnel safety, practicality
of implementation, and impact on the effectiveness of the military
readiness activity.
In evaluating how mitigation may or may not be appropriate to
ensure the least practicable adverse impact on species or stocks and
their habitat, as well as subsistence uses where applicable, we
carefully consider two primary factors:
(1) The manner in which, and the degree to which, the successful
implementation of the measure(s) is expected to reduce impacts to
marine mammals, marine mammal species or stocks, and their habitat, as
well as subsistence uses. This considers the nature of the potential
adverse impact being mitigated (likelihood, scope, range). It further
considers the likelihood that the measure will be effective if
implemented (probability of accomplishing the mitigating result if
implemented as planned), the likelihood of effective implementation
(probability implemented as planned), and;
(2) The practicability of the measures for applicant
implementation, which may consider such things as cost, impact on
operations, and, in the case of a military readiness activity,
personnel safety, practicality of implementation, and impact on the
effectiveness of the military readiness activity.
Mitigation for Marine Mammals and Their Habitat
Ships operated by or for the Navy have personnel assigned to stand
watch at all times, day and night, when moving through the water. While
in transit, ships must use extreme caution and proceed at a safe speed
such that the ship can take proper and effective action to avoid a
collision with any marine mammal and can be stopped within a distance
appropriate to the prevailing circumstances and conditions.
During navigational source deployments, visual observation would
start 30 minutes prior to and continue throughout the deployment within
an exclusion zone of 55 m (180 ft, roughly one ship length) around the
deployed mooring. Deployment will stop if a marine mammal is visually
detected within the exclusion zone. Deployment will re-commence if any
one of the following conditions are met: (1) The animal is observed
exiting the exclusion zone, (2) the animal is thought to have exited
the exclusion zone based on its course and speed, or (3) the exclusion
zone has been clear from any additional sightings for a period of 15
minutes for pinnipeds and 30 minutes for cetaceans. Visual monitoring
will continue through 30 minutes following the deployment of sources.
[[Page 37260]]
Once deployed, the spiral wave beacon would transmit for five days.
The ship will maintain position near the moored source and will monitor
the surrounding area for marine mammals. Transmission will cease if a
marine mammal enters a 55-m (180 ft) exclusion zone. Transmission will
re-commence if any one of the following conditions are met: (1) The
animal is observed exiting the exclusion zone, (2) the animal is
thought to have exited the exclusion zone based on its course and speed
and relative motion between the animal and the source, or (3) the
exclusion zone has been clear from any additional sightings for a
period of 15 minutes for pinnipeds and 30 minutes for cetaceans. The
spiral wave beacon source will only transmit during daylight hours.
Ships would avoid approaching marine mammals head on and would
maneuver to maintain an exclusion zone of 1,500 ft (457 m) around
observed mysticete whales, and 600 ft (183 m) around all other marine
mammals, provided it is safe to do so in ice free waters.
With the exception of the spiral wave beacon, moored/drifting
sources are left in place and cannot be turned off until the following
year during ice free months. Once they are programmed they will operate
at the specified pulse lengths and duty cycles until they are either
turned off the following year or there is failure of the battery and
are not able to operate. Due to the ice covered nature of the Arctic is
in not possible to recover the sources or interfere with their transmit
operations in the middle of the deployment.
These requirements do not apply if a vessel's safety is at risk,
such as when a change of course would create an imminent and serious
threat to safety, person, vessel, or aircraft, and to the extent
vessels are restricted in their ability to maneuver. No further action
is necessary if a marine mammal other than a whale continues to
approach the vessel after there has already been one maneuver and/or
speed change to avoid the animal. Avoidance measures should continue
for any observed whale in order to maintain an exclusion zone of 1,500
ft (457 m).
All personnel conducting on-ice experiments, as well as all
aircraft operating in the study area, are required to maintain a
separation distance of 1,000 ft (305 m) from any sighted marine mammal.
Based on our evaluation of the applicant's proposed measures, NMFS
has preliminarily determined that the proposed mitigation measures
provide the means effecting the least practicable impact on the
affected species or stocks and their habitat, paying particular
attention to rookeries, mating grounds, areas of similar significance,
and on the availability of such species or stock for subsistence uses.
Proposed Monitoring and Reporting
In order to issue an IHA 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
authorizations 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. Effective reporting is critical both to
compliance as well as ensuring that the most value is obtained from the
required monitoring.
Monitoring and reporting requirements prescribed by NMFS should
contribute to improved understanding of one or more of the following:
Occurrence of marine mammal species or stocks in the area
in which take is anticipated (e.g., presence, abundance, distribution,
density);
Nature, scope, or context of likely marine mammal exposure
to potential stressors/impacts (individual or cumulative, acute or
chronic), through better understanding of: (1) Action or environment
(e.g., source characterization, propagation, ambient noise); (2)
affected species (e.g., life history, dive patterns); (3) co-occurrence
of marine mammal species with the action; or (4) biological or
behavioral context of exposure (e.g., age, calving or feeding areas);
Individual marine mammal responses (behavioral or
physiological) to acoustic stressors (acute, chronic, or cumulative),
other stressors, or cumulative impacts from multiple stressors;
How anticipated responses to stressors impact either: (1)
Long-term fitness and survival of individual marine mammals; or (2)
populations, species, or stocks;
Effects on marine mammal habitat (e.g., marine mammal prey
species, acoustic habitat, or other important physical components of
marine mammal habitat); and
Mitigation and monitoring effectiveness.
While underway, the ships (including non-Navy ships operating on
behalf of the Navy) utilizing active acoustics will have at least one
watch person during activities. Watch personnel undertake extensive
training in accordance with the U.S. Navy Lookout Training Handbook or
civilian equivalent, including on the job instruction and a formal
Personal Qualification Standard program (or equivalent program for
supporting contractors or civilians), to certify that they have
demonstrated all necessary skills (such as detection and reporting of
floating or partially submerged objects). Additionally, watch personnel
have taken the Navy's Marine Species Awareness Training. Their duties
may be performed in conjunction with other job responsibilities, such
as navigating the ship or supervising other personnel. While on watch,
personnel employ visual search techniques, including the use of
binoculars, using a scanning method in accordance with the U.S. Navy
Lookout Training Handbook or civilian equivalent. A primary duty of
watch personnel is to detect and report all objects and disturbances
sighted in the water that may be indicative of a threat to the ship and
its crew, such as debris, or surface disturbance. Per safety
requirements, watch personnel also report any marine mammals sighted
that have the potential to be in the direct path of the ship as a
standard collision avoidance procedure.
The U.S. Navy has coordinated with NMFS to develop an overarching
program plan in which specific monitoring would occur. This plan is
called the Integrated Comprehensive Monitoring Program (ICMP) (Navy
2011). The ICMP has been developed in direct response to Navy
permitting requirements established through various environmental
compliance efforts. As a framework document, the ICMP applies by
regulation to those activities on ranges and operating areas for which
the Navy is seeking or has sought incidental take authorizations. The
ICMP is intended to coordinate monitoring efforts across all regions
and to allocate the most appropriate level and type of effort based on
a set of standardized research goals, and in acknowledgement of
regional scientific value and resource availability.
The ICMP is focused on Navy training and testing ranges where the
majority of Navy activities occur regularly as those areas have the
greatest potential for being impacted. ONR's Arctic Research Activities
in comparison is a less intensive test with little human activity
present in the Arctic. Human presence is limited to a minimal amount of
days for source operations and source deployments, in contrast to the
large majority (>95%) of time that the sources
[[Page 37261]]
will be left behind and operate autonomously. Therefore, a dedicated
monitoring project is not warranted. However, ONR will record all
observations of marine mammals, including the marine mammal's location
(latitude and longitude), behavior, and distance from project
activities, including icebreaking.
The Navy is committed to documenting and reporting relevant aspects
of research and testing activities to verify implementation of
mitigation, comply with permits, and improve future environmental
assessments. If any injury or death of a marine mammal is observed
during the 2019-20 Arctic Research Activities, the Navy will
immediately halt the activity and report the incident to the Office of
Protected Resources, NMFS, and the Alaska Regional Stranding
Coordinator, NMFS. The following information must be provided:
Time, date, and location of the discovery;
Species identification (if known) or description of the
animal(s) involved;
Condition of the animal(s) (including carcass condition if
the animal is dead);
Observed behaviors of the animal(s), if alive;
If available, photographs or video footage of the
animal(s); and
General circumstances under which the animal(s) was
discovered (e.g., during use of towed acoustic sources, deployment of
moored or drifting sources, during on-ice experiments, or by transiting
vessel).
ONR will provide NMFS with a draft exercise monitoring report
within 90 days of the conclusion of the proposed activity. The draft
exercise monitoring report will include data regarding acoustic source
use and any mammal sightings or detection will be documented. The
report will include the estimated number of marine mammals taken during
the activity. The report will also include information on the number of
shutdowns recorded. If no comments are received from NMFS within 30
days of submission of the draft final report, the draft final report
will constitute the final report. If comments are received, a final
report must be submitted within 30 days after receipt of comments.
Negligible Impact Analysis and Determination
NMFS has defined negligible impact 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 (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 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 harassment, NMFS considers other factors, such as the
likely nature of any responses (e.g., intensity, duration), the context
of any responses (e.g., critical reproductive time or location,
migration), as well as effects on habitat, and the likely effectiveness
of the mitigation. We also assess the number, intensity, and context of
estimated takes by evaluating this information relative to population
status. Consistent with the 1989 preamble for NMFS's implementing
regulations (54 FR 40338; September 29, 1989), the impacts from other
past and ongoing anthropogenic activities are incorporated into this
analysis via their impacts on the environmental baseline (e.g., as
reflected in the regulatory status of the species, population size and
growth rate where known, ongoing sources of human-caused mortality, or
ambient noise levels).
Underwater acoustic transmissions associated with the Arctic
Research Activities, as outlined previously, have the potential to
result in Level B harassment of beluga whales, ringed seals, and
bearded seals in the form of TTS and behavioral disturbance. No serious
injury, mortality, or Level A harassment are anticipated to result from
this activity.
Minimal takes of marine mammals by Level B harassment would be due
to TTS since the range to TTS effects is small at only 12 m or less
while the behavioral effects range is significantly larger extending up
to 20 km (Table 7). TTS is a temporary impairment of hearing and can
last from minutes or hours to days (in cases of strong TTS). In many
cases, however, hearing sensitivity recovers rapidly after exposure to
the sound ends. No takes from TTS were modeled, but if TTS did occur,
the overall fitness of the individual is unlikely to be affected and
negative impacts to the relevant stock are not anticipated.
Effects on individuals that are taken by Level B harassment could
include alteration of dive behavior, alteration of foraging behavior,
effects to breathing rates, interference with or alteration of
vocalization, avoidance, and flight. More severe behavioral responses
are not anticipated due to the localized, intermittent use of active
acoustic sources. Most likely, individuals will simply be temporarily
displaced by moving away from the sound source. As described previously
in the behavioral effects section, seals exposed to non-impulsive
sources with a received sound pressure level within the range of
calculated exposures (142-193 dB re 1 [micro]Pa), have been shown to
change their behavior by modifying diving activity and avoidance of the
sound source (G[ouml]tz et al., 2010; Kvadsheim et al., 2010). Although
a minor change to a behavior may occur as a result of exposure to the
sound sources associated with the proposed action, these changes would
be within the normal range of behaviors for the animal (e.g., the use
of a breathing hole further from the source, rather than one closer to
the source, would be within the normal range of behavior). Thus, even
repeated Level B harassment of some small subset of the overall stock
is unlikely to result in any significant realized decrease in fitness
for the affected individuals, and would not result in any adverse
impact to the stock as a whole.
The project is not expected to have significant adverse effects on
marine mammal habitat. While the activities may cause some fish to
leave the area of disturbance, temporarily impacting marine mammals'
foraging opportunities, this would encompass a relatively small area of
habitat leaving large areas of existing fish and marine mammal foraging
habitat unaffected. Icebreaking may temporarily affect the availability
of pack ice for seals to haul out but the proportion of ice disturbed
is small relative to the overall amount of available ice habitat.
Icebreaking will not occur during the time of year when ringed seals
are expected to be within subnivean lairs or pupping (Chapskii 1940;
McLaren 1958; Smith and Stirling 1975). As such, the impacts to marine
mammal habitat are not expected to cause significant or long-term
negative consequences.
In summary and as described above, the following factors primarily
support our preliminary determination that the impacts resulting from
this activity are not expected to adversely affect the species or stock
through effects on annual rates of recruitment or survival:
No mortality is anticipated or authorized;
Impacts will be limited to Level B harassment;
Takes by Level B harassment will primarily be in the form
of behavioral disturbance; and
There will be no permanent or significant loss or
modification of marine mammal prey or habitat.
[[Page 37262]]
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 the proposed activity will have a negligible impact on
all affected marine mammal species or stocks.
Unmitigable Adverse Impact Analysis and Determination
Impacts to subsistence uses of marine mammals resulting from the
proposed action are not anticipated. The closest active acoustic source
within the study area is approximately 145 mi (233 km) from land,
outside of known subsistence use areas. Based on this information, NMFS
has preliminarily determined that there will be no unmitigable adverse
impact on subsistence uses from ONR's proposed activities.
Endangered Species Act (ESA)
Section 7(a)(2) of the Endangered Species Act of 1973 (16 U.S.C.
1531 et seq.) requires that each Federal agency insure that any action
it authorizes, funds, or carries out is not likely to jeopardize the
continued existence of any endangered or threatened species or result
in the destruction or adverse modification of designated critical
habitat. To ensure ESA compliance for the issuance of IHAs, NMFS
consults internally, in this case with the NMFS Alaska Regional Office
(AKR), whenever we propose to authorize take for endangered or
threatened species.
NMFS is proposing to authorize take of ringed seals and bearded
seals, which are listed under the ESA. The Permits and Conservation
Division has requested initiation of section 7 consultation with the
Protected Resources Division of AKR for the issuance of this IHA. NMFS
will conclude the ESA consultation prior to reaching a determination
regarding the proposed issuance of the authorization.
Proposed Authorization
As a result of these preliminary determinations, NMFS proposes to
issue an IHA to ONR for conducting Arctic Research Activities in the
Beaufort and Chukchi Seas, provided the previously mentioned
mitigation, monitoring, and reporting requirements are incorporated. A
draft of the proposed IHA can be found at https://www.fisheries.noaa.gov/permit/incidental-take-authorizations-under-marine-mammal-protection-act.
Request for Public Comments
We request comment on our analyses, the proposed authorization, and
any other aspect of this Notice of Proposed IHA for the proposed
action. We also request at this time comment on the potential renewal
of this proposed IHA as described in the paragraph below. Please
include with your comments any supporting data or literature citations
to help inform decisions on the request for this IHA or a subsequent
Renewal.
On a case-by-case basis, NMFS may issue a one-year IHA renewal with
an additional 15 days for public comments when (1) another year of
identical or nearly identical activities as described in the Specified
Activities section of this notice is planned or (2) the activities as
described in the Specified Activities section of this notice would not
be completed by the time the IHA expires and a second IHA would allow
for completion of the activities beyond that described in the Dates and
Duration section of this notice, provided all of the following
conditions are met:
A request for renewal is received no later than 60 days
prior to expiration of the current IHA;
The request for renewal must include the following:
(1) An explanation that the activities to be conducted under the
requested Renewal are identical to the activities analyzed under the
initial IHA, are a subset of the activities, or include changes so
minor (e.g., reduction in pile size) that the changes do not affect the
previous analyses, mitigation and monitoring requirements, or take
estimates (with the exception of reducing the type or amount of take
because only a subset of the initially analyzed activities remain to be
completed under the Renewal); and
(2) A preliminary monitoring report showing the results of the
required monitoring to date and an explanation showing that the
monitoring results do not indicate impacts of a scale or nature not
previously analyzed or authorized.
Upon review of the request for Renewal, the status of the
affected species or stocks, and any other pertinent information, NMFS
determines that there are no more than minor changes in the activities,
the mitigation and monitoring measures will remain the same and
appropriate, and the findings in the initial IHA remain valid.
Dated: July 26, 2019.
Catherine Marzin,
Acting Director, Office of Protected Resources, National Marine
Fisheries Service.
[FR Doc. 2019-16318 Filed 7-30-19; 8:45 am]
BILLING CODE 3510-22-P