Taking and Importing Marine Mammals; U.S. Navy's Research, Development, Test, and Evaluation Activities Within the Naval Sea Systems Command Naval Undersea Warfare Center Keyport Range Complex, 32264-32305 [E9-15839]
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FOR FURTHER INFORMATION CONTACT:
Shane Guan, Office of Protected
Resources, NMFS, (301) 713–2289, ext.
137.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 218
RIN 0648–AX11
Taking and Importing Marine
Mammals; U.S. Navy’s Research,
Development, Test, and Evaluation
Activities Within the Naval Sea
Systems Command Naval Undersea
Warfare Center Keyport Range
Complex
AGENCY: National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Proposed rule; request for
comments.
SUMMARY: NMFS has received a request
from the U.S. Navy (Navy) for
authorization to take marine mammals
incidental to the Navy’s Research,
Development, Test, and Evaluation
(RDT&E) activities within the Naval Sea
System Command (NAVSEA) Naval
Undersea Warfare Center (NUWC)
Keyport Range Complex and the
associated proposed extensions for the
period of September 2009 through
September 2014. Pursuant to the Marine
Mammal Protection Act (MMPA), NMFS
is proposing regulations to govern that
take and requesting information,
suggestions, and comments on these
proposed regulations.
DATES: Comments and information must
be received no later than August 6,
2009.
ADDRESSES: You may submit comments,
identified by 0648–AX11, by any one of
the following methods:
• Electronic Submissions: Submit all
electronic public comments via the
Federal eRulemaking Portal https://
www.regulations.gov
• Hand delivery or mailing of paper,
disk, or CD–ROM: Comments should be
addressed to Michael Payne, Chief,
Permits, Conservation and Education
Division, Office of Protected Resources,
National Marine Fisheries Service, 1315
East-West Highway, Silver Spring, MD
20910–3225.
Instructions: All comments received
are a part of the public record and will
generally be posted to https://
www.regulations.gov without change.
All personal identifying information (for
example, name, address, etc.)
voluntarily submitted by the commenter
may be publicly accessible. Do not
submit Confidential Business
Information or otherwise sensitive or
protected information.
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Availability
A copy of the Navy’s application may
be obtained by writing to the address
specified above (see ADDRESSES),
telephoning the contact listed above (see
FOR FURTHER INFORMATION CONTACT), or
visiting the internet at: https://
www.nmfs.noaa.gov/pr/permits/
incidental.htm. The Navy’s Draft
Environmental Impact Statement (DEIS)
for the Keyport Range Complex RDT&E
and range extension activities was
published on September 12, 2008, and
may be viewed at https://wwwkeyport.kpt.nuwc.navy.mil. NMFS
participated in the development of the
Navy’s DEIS as a cooperating agency
under the National Environmental
Policy Act (NEPA).
Background
Sections 101(a)(5)(A) and (D) of the
MMPA (16 U.S.C. 1361 et seq.) direct
the Secretary of Commerce (Secretary)
to allow, upon request, the incidental,
but not intentional taking of marine
mammals by U.S. citizens who engage
in a specified activity (other than
commercial fishing) during periods of
not more than five consecutive years
each if certain findings are made and
regulations are issued or, if the taking is
limited to harassment, notice of a
proposed authorization is provided to
the public for review.
Authorization shall be granted if
NMFS finds that the taking will have a
negligible impact on the species or
stock(s), will not have an unmitigable
adverse impact on the availability of the
species or stock(s) for subsistence uses,
and if the permissible methods of taking
and requirements pertaining to the
mitigation, monitoring and reporting of
such taking are set forth. NMFS has
defined ‘‘negligible impact’’ in 50 CFR
216.103 as:
An impact resulting from the specified
activity that cannot be reasonably expected
to, and is not reasonably likely to, adversely
affect the species or stock through effects on
annual rates of recruitment or survival.
The National Defense Authorization
Act of 2004 (NDAA) (Public Law 108–
136) removed the ‘‘small numbers’’ and
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‘‘specified geographical region’’
limitations in sections 101(a)(5)(A) and
(D) and amended the definition of
‘‘harassment’’ as it applies to a ‘‘military
readiness activity’’ to read as follows
(Section 3(18)(B) of the MMPA):
(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].
Summary of Request
On May 15, 2008, NMFS received an
application from the Navy requesting
authorization for the take of 5 species of
marine mammals incidental to the
RDT&E activities within the NAVSEA
NUWC Keyport Range Complex
Extension over the course of 5 years.
These RDT&E activities are classified as
military readiness activities. On April
29, 2009, NMFS received additional
information and clarification on the
Navy’s proposed NAVSEA NUWC
Keyport Range Complex Extension
RDT&E activities. The Navy states that
these RDT&E activities may cause
various impacts to marine mammal
species in the proposed action area. The
Navy requests an authorization to take
individuals of these marine mammals
by Level B Harassment. Please refer to
Tables 6–23, 6–24, 6–25, and 6–26 of
the Navy’s Letter of Authorization
(LOA) application for detailed
information of the potential marine
mammal exposures from the RDT&E
activities in the Keyport Range Complex
Extension per year. However, due to the
proposed mitigation and monitoring
measures and standard range operating
procedures in place, NMFS estimates
that the take of marine mammals is
likely to be lower than the amount
requested. NMFS does not expect any
marine mammals to be killed or injured
as a result of the Navy’s proposed
activities, and NMFS is not proposing to
authorize any injury or mortality
incidental to the Navy’s proposed
RDT&E activities within the Keyport
Range Complex Extension.
Background of Navy Request
The Navy proposes to extend the
NAVSEA NUWC Keyport Range
Complex in Washington State. The
NAVSEA NUWC Keyport Range
Complex has the infrastructure to
support RDT&E activities. Centrally
located within Washington State, the
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NAVSEA NUWC Keyport Range
Complex has extensive existing range
assets and capabilities. The NAVSEA
NUWC Keyport Range Complex is
composed of Keyport Range Site, Dabob
Bay Range Complex (DBRC) Site, and
Quinault Underwater Tracking Range
(QUTR) Site (see Figure 1–1 of the
Navy’s LOA application).
The goal of the Proposed Action is to
extend the operational areas of each
range site. Extending the Range
Complex operating areas outside
existing range boundaries will allow the
Navy to support existing and future
range activities including evolving
manned and unmanned vehicle program
needs in multiple marine environments.
With the proposed extension of the
Keyport and QUTR range sites, the
range sites could support more
activities, which include increases in
the numbers of tests and days of testing.
No additional operational tempo is
proposed for the DBRC Site. Existing
and evolving range activities applied for
in this LOA application include RDT&E
and training of system capabilities such
as guidance, control, and sensor
accuracy of manned and unmanned
vehicles in multiple marine
environments (e.g., differing depths,
salinity levels, temperatures, sea states,
etc.).
The range extension is necessary to
provide adequate testing area and
volume (i.e., surface area and water
depth) in multiple marine
environments. The extension enables
the NUWC Keyport to fulfill its mission
of providing test and evaluation services
in both surrogate and simulated warfighting environments for emerging
manned and unmanned vehicle program
activities. Within the NAVSEA NUWC
Keyport Range Complex Extension, the
NUWC Keyport activities include
testing, training, and evaluation of
systems capabilities such as guidance,
control, and sensor accuracy of manned
and unmanned vehicles in multiple
marine environments (e.g., differing
depths, salinity levels, temperatures, sea
states, etc.).
NUWC Keyport consists of 340 acres
(138 hectares [ha]) on the shores of
Liberty Bay and Port Orchard Reach
(a.k.a. Port Orchard Narrows), and is
located adjacent to the town of Keyport,
due west of Seattle. NUWC Keyport, a
part of NAVSEA, is the center for
integrated undersea warfare systems
dependability, integrated mine and
undersea warfare supportability, and
undersea vehicle maintenance and
engineering. It provides test and
evaluation, in-service engineering,
maintenance, Fleet readiness, and
industrial-based support for undersea
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warfare systems, including RDT&E of
torpedoes, unmanned vehicles, sensors,
targets, countermeasure systems, and
acoustic systems.
The NAVSEA NUWC Keyport Range
Complex is divided into open ocean/
offshore areas and in shore areas:
• Open Ocean Area—air, surface, and
subsurface areas of the NAVSEA NUWC
Keyport Range Complex that lie outside
of 12 nautical miles (nm) from land.
• Offshore Area—air, surface, and
subsurface ocean areas within 12 nm of
the Pacific Coast.
• Inshore—air, surface, and
subsurface areas within the Puget
Sound, Port Orchard Reach, Hood
Canal, and Dabob Bay.
Keyport Range Site
Located adjacent to NUWC Keyport,
this range provides approximately 1.5
square nautical miles (nm2) (5.1 square
kilometers [km2]) of shallow underwater
testing, including in-shore shallow
water sites and a shallow lagoon to
support integrated undersea warfare
systems and vehicle maintenance and
engineering activities (see Figures 1–2
and 1–3 of the Navy’s LOA application).
The Navy has conducted underwater
testing at the Keyport Range Site since
1914. Underwater tracking of test
activities is accomplished by using
temporary or portable range equipment.
The range is currently used an average
of 6 times per year for vehicle testing
and a variety of boat and diver training
activities, each lasting 1–30 days. There
may be several activities in 1 day. The
range site also supports: (1) Detection,
classification, and localization of test
objectives and (2) magnetics
measurement programs. Explosive
warheads are not placed on test units or
tested within the Keyport Range Site.
DBRC Site
Currently, the DBRC Site assets
include the Dabob Bay Military
Operating Area (MOA), the Hood Canal
North and South MOAs adjacent to
Submarine Base (SUBASE) Bangor, and
the Connecting Waters (see Figures 1–2
and 1–4 of the Navy’s LOA application).
The DBRC Site is the Navy’s premier
location within the U.S. for RDT&E of
underwater systems such as torpedoes,
countermeasures, targets, and ship
systems. Primary activities at the DBRC
Site support proofing of underwater
systems, research and development test
support, and Fleet training and tactical
evaluations involving aircraft,
submarines, and surface ships. Tests
and evaluations of underwater systems,
from the first prototype and preproduction stages up through Fleet
activities (inception to deployment),
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ensure reliability and availability of
underwater systems and their Fleet
components. As with the Keyport Range
Site, there are no explosive warheads
tested or placed on test units.
The DBRC Site also supports acoustic/
magnetic measurement programs. These
programs include underwater vehicle/
ship noise/magnetic signature
recording, radiated sound
investigations, and other acoustic
evaluations. In the course of these
activities, various combinations of
aircraft, submarines, and surface ships
are used as launch platforms. Test
equipment may also be launched or
deployed from shore off a pier or placed
in the water by hand. NUWC Keyport
currently conducts activities within four
underwater testing areas in the DBRC
Site. These areas are:
• Dabob Bay MOA—a deep-water
range in Jefferson County approximately
14.5 nm2 (49.9 km2) in size. The
acoustic tracking space within the range
is approximately 7.3 by 1.3 nm (13.5 by
2.4 km) (9.5 nm2 [32.4 km2]) with a
maximum depth of 600 ft (183 m). The
Dabob Bay MOA is the principal range
and the only component of the DBRC
Site with extensive acoustic monitoring
instrumentation installed on the
seafloor, allowing for object tracking,
communications, passive sensing, and
target simulation.
• Hood Canal MOAs—There are two
deep-water operating areas adjacent to
SUBASE Bangor in Hood Canal: Hood
Canal MOA South, which is
approximately 4.5 nm2 (15.4 km2) in
size, and Hood Canal MOA North,
which is approximately 7.9 nm2 (27.0
km2) in size. Both areas have an average
depth of 200 ft (61 m). The Hood Canal
MOAs are used for vessel sensor
accuracy tests and launch and recovery
of test systems where tracking is
optional.
• Connecting Waters—the portion of
the Hood Canal that connects the Dabob
Bay MOA with the Hood Canal MOAs.
The shortest distance between the
Dabob Bay MOA and Hood Canal MOA
South by water is approximately 5.8
nm2 (19.8 km2). Water depth in the
Connecting Waters is typically greater
than 300 ft (91 m).
QUTR Site
The Navy has conducted underwater
testing at the QUTR Site since 1981 and
maintains a control center at the
Kalaloch Ranger Station. As at the other
range sites, no explosive warheads are
used at the QUTR Site. The QUTR Site
is a rectangular-shaped test area of about
48.3 nm2 (165.5 km2), located
approximately 6.5 nm (12 km) off the
Pacific Coast at Kalaloch, Washington. It
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lies within the boundaries of the
Olympic Coast National Marine
Sanctuary (OCNMS).
The QUTR Site is instrumented to
track surface vessels, submarines, and
various undersea vehicles. Bottom
sensors are permanently mounted on
the sea floor for tracking and are
maintained and configured by the Navy.
The sensors are connected to the shore
via cables, which extend under the
beach to the bluffs and end at a Navy
trailer in Kalaloch (National Park
Service [NPS] property). In addition,
portable range equipment may be set up
prior to conducting various activities on
the range and removed after it is no
longer needed. All communications are
sent back to NUWC Keyport for
monitoring.
This range underlies a small portion
(W–237A) of the larger airspace unit W–
237. This airspace complex comprises
the northern portion of the Pacific
Northwest Ocean Surface/Subsurface
Operating Area (OPAREA), NOAA chart
number 18500 (NOAA, 2006). Activities
in this airspace are scheduled and
coordinated with Naval Air Station
(NAS) Whidbey Island and Commander
Submarine Force, U.S. Pacific Fleet
(COMSUBPAC).
All range areas in the NAVSEA
NUWC Keyport Range Complex
Extension include areas where marine
mammals may be found. Range
activities will be conducted in the
Keyport Site, the DBRC, and the QUTR
Site. The proposed annual usage at each
site is listed in Table 1. This includes
tracking sonar systems, side-scan, and
thermal propulsion systems.
TABLE 1—PROJECTED ANNUAL DAYS OF USE BY RANGE SITE
Keyport range
site
Current .............................................................................................................
Proposed ..........................................................................................................
Description of the Specified Activities
Typical activities conducted in the
NAVSEA NUWC Keyport Range
Complex Extension on the three existing
range sites primarily support undersea
warfare RDT&E program requirements,
but they also support general equipment
test and military personnel training
needs, including Fleet activities. These
activities involve mid- and highfrequency acoustic sources with the
DBRC site
55
60
potential to affect marine mammals that
may be present within the NAVSEA
NUWC Keyport Range Complex
Extension. Current and proposed
activities within the Keyport Range
Complex Extension are listed below:
Range Activities: Testing That Involves
Active Acoustic Devices
QUTR site—
offshore
200
200
QUTR site—
surf zone
14
16
0
30
NUWC Keyport Range Complex with
information on the frequency bands is
shown in Table 2. In this document, low
frequency is defined as below 1
kiloHertz (kHz), mid frequency is
defined as between 1 kHz and 10 kHz,
and high frequency is defined as above
10 kHz.
A list of the primary active acoustic
sources used within the NAVSEA
TABLE 2—PRIMARY ACOUSTIC SOURCES COMMONLY USED WITHIN THE NAVSEA NUWC KEYPORT RANGE COMPLEX
Source
Frequency (kHz)
Sonar:
General range tracking (at Keyport Range Site) .................................................................................
General range tracking (at DBRC and QUTR Sites) ...........................................................................
UUV tracking ........................................................................................................................................
Torpedoes .............................................................................................................................................
Range targets and special tests (at Keyport Range Site) ...................................................................
Range targets and special tests (at DBRC and QUTR Sites) .............................................................
Special sonars (e.g., UUV payload) .....................................................................................................
Fleet aircraft—active sonobuoys and helo-dipping sonars ..................................................................
Side-scan ..............................................................................................................................................
Other Acoustic Sources:
Acoustic modems .................................................................................................................................
Target simulator ....................................................................................................................................
Aid to navigation (range equipment) ....................................................................................................
Sub-bottom profiler ...............................................................................................................................
10–100
10–100
10–100
10–100
5–100
5–100
100–2,500
2–20
100–700
General range tracking on the
instrumented ranges and portable range
sites have active output in relatively
wide frequency bands. Operating
frequencies are 10 to 100 kHz. At the
Keyport Range Site the sound pressure
level (SPL) of the source (source level)
is a maximum of 195 dB re 1 μPa-m. At
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the DBRC and QUTR sites, the source
level for general range tracking is a
maximum of 203 dB re 1 μPa-m.
(2) UUV Tracking Systems
UUV tracking systems operate at
frequencies of 10 to 100 kHz with
maximum source levels of 195 dB re 1
μPa-m at all range sites.
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195
203
195
233
195
238
235
225
235
10–300
0.1–10
70–80
2–7
35–45
0.05–10
Engine noise (surface vessels, submarines, torpedoes, UUVs) ..........................................................
(1) General Range Tracking
Maximum source
level
(dB re 1 μPa-m)
210
170
210
210
220
170
(3) Torpedo Sonars
Torpedo sonars are used for several
purposes including detection,
classification, and location and vary in
frequency from 10 to 100 kHz. The
maximum source level of a torpedo
sonar is 233 dB re 1 μPa-m.
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(4) Range Targets and Special Tests
Range targets and special test systems
are within the 5 to 100 kHz frequency
range at the Keyport Range Site with a
maximum source level of 195 dB re 1
μPa-m. At the DBRC and QUTR sites,
the maximum source level is 238 dB re
1 μPa-m.
(5) Special Sonars
Special sonars can be carried as a
payload on a UUV, suspended from a
range craft, or set on or above the sea
floor. These can vary widely from 100
kHz to a very high frequency of 2,500
kHz for very short range detection and
classification. The maximum source
level of these acoustic sources is 235 dB
re 1 μPa-m.
(6) Sonobuoys and Helicopter Dipping
Sonar
Sonobuoys and helicopter dipping
sonars are deployed from Fleet aircraft
and operate at frequencies of 2 to 20
kHz with maximum source levels of 225
dB re 1 μPa-m. Dipping sonars are active
or passive devices that are lowered on
cable by helicopters or surface vessels to
detect or maintain contact with
underwater targets.
(7) Side Scan Sonar
Side-scan sonar is used for mapping,
detection, classification, and
localization of items on the sea floor
such as cabling, shipwrecks, and mine
shapes. It is high frequency typically
100 to 700 kHz using multiple
frequencies at one time with a very
directional focus. The maximum source
level is 235 dB re 1 μPa-m. Side-scan
and multibeam sonar systems are towed
or mounted on a test vehicle or ship.
(8) Other Acoustic Sources
Other acoustic sources may include
acoustic modems, targets, aids to
navigation, subbottom profilers, and
engine noise.
• An acoustic modem is a
communication device that transmits an
acoustically encoded signal from a
source to a receiver. Acoustic modems
emit pulses from 10 to 300 kHz at
source levels less than 210 dB re 1 μPam.
• Target simulators operate at
frequencies of 100 Hertz (Hz) (0.1 kHz)
to 10 kHz at source levels of less than
170 dB re 1 μPa-m.
• Aids to navigation transmit location
data from ship to shore and back to ship
so the crew can have real-time detailed
location information. This is typical of
the range equipment used in support of
testing. New aids to navigation can also
be deployed and tested using 70 to 80
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kHz at source levels less than 210 dB re
1 μPa-m.
• Subbottom profilers are often
commercial off-the-shelf sonars used to
determine characteristics of the sea
bottom and subbottom such as mud
above bedrock or other rocky substrate.
These operate at 2 to 7 kHz at source
levels less than 210 dB re 1 μPa-m, and
35 to 45 kHz at less than 220 dB re 1
μPa-m.
• There are many sources of engine
noise including but not limited to
surface vessels, submarines, torpedoes,
and other UUVs. The acoustic energy
generally ranges from 50 Hz to 10 kHz
at source levels less than 170 dB re 1
μPa-m. Targets, both mobile and
stationary, may simulate engine noise at
these same frequencies.
Additionally, a variety of surface
vessels operate active acoustic depth
sensors (fathometers) within the range
sites, including Navy, private, and
commercial vessels. In some cases, one
or more frequencies are projected
underwater. Bottom type, depth
contours, and objects (e.g., cables,
sunken ships) can be located using this
equipment. The depth sensors used by
NUWC Keyport are the same
fathometers used by commercial and
recreational vessels for navigational
safety. Because these instruments are
widely used and are not found to
adversely impact the human or natural
environment, they are not analyzed
further.
Range Activities: Testing That Involves
Non-Acoustic Activities
(1) Magnetic
There are two types: (a) Magnetic
sensors, and (b) magnetic sources.
Magnetic sensors are passive and do not
have a magnetic field associated with
them. The sensors are bottom mounted,
over the side (stationary or towed) or
can be integrated into a UUV. They are
used to sense the magnetic field of an
object such as a surface vessel, a
submarine, or a buried target. Magnetic
sources are used to represent magnetic
targets or are energized items such as
power cables for energy generators (e.g.
tidal). Magnetic sources generate
electromagnetic fields (EMF).
Evaluation of EMF (Navy 2008a) has
shown that sources (e.g. Organic
Airborne and Surface Influence Sweep
(OASIS)) used are typically below 23
gauss (G) and are considered relatively
minute strength.
(2) Oceanographic Sensor
These sensors have been used
historically to determine marine
characteristics such as conductivity,
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temperature, and pressure of water to
determine sound velocity in water. This
provides information about how sound
will travel through the water. These
sensors can be deployed over the side
from a surface craft, suspended in water,
or carried on a UUV.
(3) Laser Imaging Detection and Ranging
(LIDAR)
Also known as light detection and
ranging, LIDAR is used to measure
distance, speed, rotation, and chemical
composition and concentration of
remote solid objects such as a ship or
submerged object. LIDAR uses the same
principle as radar. The LIDAR
instrument transmits short pulses of
laser light towards the target. The
transmitted light interacts with and is
changed by the target. Some of this light
is reflected back to the instrument
where it is analyzed. The change in the
properties of the light enables some
property of the target to be determined.
The time it takes the light to travel to
the target and back to the LIDAR can be
used to determine the distance to the
target. Since light attenuates rapidly in
water, underwater LIDAR uses light in
the blue-green part of the spectrum as it
attenuates the least. Common civilian
uses of LIDAR in the ocean include
seabed mapping and fish detection. All
safety issues associated with the use of
lasers are evaluated for all applicable
test activities within the range sites
according to Navy and Federal
regulations. This bounds the intensity of
LIDAR used pursuant to this request to
those systems that meet human safety
standards.
(4) Inert Mine Hunting and Inert Mine
Clearing Exercises
Associated with testing, a series of
inert mine shapes are set out in a
uniform or random pattern to test the
detection, classification and localization
capability of the system under test. They
are made from plastic, metal, and
concrete and vary in shape. An inert
mine shape can measure about 10 by
1.75 ft (3 by 0.5 m) and weigh about 800
lbs (362 kg). Inert mine shapes either sit
on the bottom or are tethered by an
anchor to the bottom at various depths.
Inert mine shapes can be placed
approximately 200–300 yards (183–274
m) apart using a support craft and
remain on the bottom until they need to
be removed. All major components of
all inert mine systems used as ‘targets’
for inert mine hunting systems are
removed within 2 years.
NMFS does not believe that those
Range activities that involve nonacoustic testing will have adverse
impacts to marine mammals, therefore,
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they are not analyzed further and will
not be covered under the proposed rule.
increase in average annual days of use
due to the range extension at this site.
Increased Activities Due to Range
Extension
annual days of use of the Keyport Range
Site would increase from the current 55
days to 60 days.
(2) DBRC Site
The southern boundary of DBRC Site
would be extended to the Hamma
Hamma River and its northern boundary
would be extended to 1 nm (2 km) south
of the Hood Canal Bridge (Highway
104). This extension would increase the
size of the current operating area from
approximately 32.7 nm2 (112.1 km2) to
approximately 45.7 nm2 (150.8 km2)
and would afford a straight run of
approximately 27.5 nm (50.9 km). There
would be no change in the number and
types of activities from the existing
range activities at DBRC Site, and no
Range boundaries of QUTR Site
would be extended to coincide with the
overlying special use airspace of W–
237A plus a 7.8 nm2 (26.6 km2) surf
zone at Pacific Beach. The total range
area would increase from approximately
48.3 nm2 (165.5 km2) to approximately
1,839.8 nm2 (6,310.2 km2). The average
annual number of days of use for
offshore activities would increase from
14 days/year to 16 days/year in the
offshore area. The average annual days
of use for surf-zone activities would
increase from 0 days/year to 30 days/
year.
context for each species. The data were
compiled from available sighting
records, literature, satellite tracking, and
stranding and by-catch data.
A total of 24 cetacean species and
subspecies and 5 pinniped species are
known to occur in Washington State
waters; however, several are seen only
rarely. Seven of these marine mammal
species are listed as Federally-
endangered under the Endangered
Species Act (ESA) occur or have the
potential to occur in the proposed
action area: blue whale (Balaenoptera
musculus), fin whale (B. physalus), Sei
whale (B. borealis), humpback whale
(Megaptera novaengliae), north Pacific
right whale (Eubalaena japonica), sperm
whale (Physeter macrocephalus), and
the southern resident population of
(1) Keyport Range Site
Range boundaries of the Keyport
Range Site would be extended to the
north, east and south, increasing the
size of the range from 1.5 nm2 to 3.2
nm2 (5.1 km2 to 11.0 km2). The average
Description of Marine Mammals in the
Area of the Specified Activities
The information on marine mammals
and their distribution and density are
based on the data gathered from NMFS,
United States Fish and Wildlife Service
(USFWS) and recent references,
literature searches of search engines,
peer review journals, and other
technical reports, to provide a regional
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The proposed range extension would
expand the geographic area for all three
range sites and increase the tempo of
activities in the Keyport and QUTR
ranges sites. A detailed list of the
proposed annual range is provided in
Table 3.
(3) QUTR Site
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killer whales (Orcinus orca). The
species, Steller sea lion (Eumetopias
jubatus), is listed as threatened under
the ESA.
Survey data concerning the inland
waters of Puget Sound are sparse. There
have been few comprehensive studies of
marine mammals in inland waters, and
those that have occurred have focused
on inland waters farther north (Strait of
Juan de Fuca, San Juan/Gulf Islands,
Strait of Georgia) (Osmek et al., 1998).
Most published information focuses on
single species (e.g., harbor seals, Jeffries
et al., 2003) or are stock assessment
reports published by NMFS (e.g.,
Carretta et al., 2008).
Survey data for the offshore waters of
Washington State, including the area of
the QUTR Site, are somewhat better,
particularly for cetaceans. The NMFS
conducted vessel surveys in the region
in 1996 and 2001, which are
summarized in Barlow (2003) and
Appler et al. (2004). Vessel surveys
were again conducted by NMFS in
summer 2005, and included finer-scale
survey lines within the OCNMS
(Forney, 2007). Cetacean densities from
this most recent effort were used
wherever possible; older density values
(2001 or 1996) were used when more
recent values were not available. Some
cetacean densities (gray and killer
whale, harbor porpoise) were obtained
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from sources other than the broad scale
surveys indicated above and the
methodologies of deriving the densities
are included in the Navy’s LOA
application.
Pinniped at-sea density is not often
available because pinniped abundance
is most often obtained via shore counts
of animals at known rookeries and
haulouts. Therefore, densities of
pinnipeds were derived differently from
those of cetaceans. Several parameters
were identified from the literature,
including area of stock occurrence,
number of animals (which may vary
seasonally) and season, and those
parameters were then used to calculate
density. Determining density in this
manner is risky as the parameters used
usually contain error (e.g., geographic
range is not exactly known and needs to
be estimated, abundance estimates
usually have large variances) and, as is
true of all density estimates, they
assume that animals are always
distributed evenly within an area,
which is likely rarely true. However,
this remains one of the few means
available to determine at-sea density for
pinnipeds.
Sea otters occur along the northern
Washington coast. Density of sea otters
was published as animals/km, which
was modified to provide density per
area. Since sea otters are under the U.S.
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Fish and Wildlife Service jurisdiction,
they are not considered in this
document.
The following are brief descriptions of
the temporal and spatial distribution
and abundance of marine mammals
throughout the NAVSEA NUWC
Keyport Range Complex Extension.
Keyport Range Site
A total of five cetaceans and three
pinnipeds are known to occur within
central Puget Sound, which
encompasses the Keyport action area,
but several of these species have never
been observed in Port Orchard Narrows
or in the action area (Table 4).
Humpback whales, minke whales, killer
whales, and Steller sea lions are
expected to be uncommon to rare in
southern Puget Sound and have never
been seen in the Keyport action area.
Density estimates for these species are
available for Puget Sound as a whole,
but since these species have never been
recorded or observed in the action area,
the densities for the action area are
shown as ‘‘0’’ to reflect this. The
proposed extension area of the Keyport
Range Site is listed as critical habitat for
Southern Resident killer whales. The
current Keyport Range Site is outside
the critical habitat area.
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DBRC Site
Six cetaceans and three pinnipeds are
known to occur or potentially occur
within the DBRC action area (Table 5).
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Density estimates for these species are
available for Puget Sound as a whole,
but since these species have never been
recorded or observed in the action area,
the densities for the action area are
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shown as ‘‘0’’ to reflect this. There is no
designated or proposed critical habitat
for marine mammals within the DBRC
action area.
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QUTR Site
The diversity of marine mammals that
occur in QUTR is greater than that in
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the Puget Sound ranges and is listed in
Table 6.
BILLING CODE 3510–22–P
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More detailed description of marine
mammal density estimates within the
NAVSEA NUWC Keyport Range
Complex Extension is provided in the
Navy’s LOA application.
A Brief Background on Sound
An understanding of the basic
properties of underwater sound is
necessary to comprehend many of the
concepts and analyses presented in this
document. A summary is included
below.
Sound is a wave of pressure variations
propagating through a medium (for the
sonar considered in this proposed rule,
the medium is marine water). Pressure
variations are created by compressing
and relaxing the medium. Sound
measurements can be expressed in two
forms: intensity and pressure. Acoustic
intensity is the average rate of energy
transmitted through a unit area in a
specified direction and is expressed in
watts per square meter (W/m2). Acoustic
intensity is rarely measured directly, it
is derived from ratios of pressures; the
standard reference pressure for
underwater sound is 1 microPascal
(microPa); for airborne sound, the
standard reference pressure is 20
microPa (Urick, 1983).
Acousticians have adopted a
logarithmic scale for sound intensities,
which is denoted in decibels (dB).
Decibel measurements represent the
ratio between a measured pressure value
and a reference pressure value (in this
case 1 microPa or, for airborne sound,
20 microPa). The logarithmic nature of
the scale means that each 10 dB increase
is a tenfold increase in power (e.g., 20
dB is a 100-fold increase, 30 dB is a
1,000-fold increase). Humans perceive a
10-dB increase in noise as a doubling of
sound level, or a 10 dB decrease in
noise as a halving of sound level. The
term ‘‘sound pressure level’’ implies a
decibel measure and a reference
pressure that is used as the denominator
of the ratio. Throughout this document,
NMFS uses 1 microPa as a standard
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reference pressure unless noted
otherwise.
It is important to note that decibels
underwater and decibels in air are not
the same and cannot be directly
compared. To estimate a comparison
between sound in air and underwater,
because of the different densities of air
and water and the different decibel
standards (i.e., reference pressures) in
water and air, a sound with the same
intensity (i.e., power) in air and in water
would be approximately 61.5 dB lower
in air. Thus, a sound that is 160 dB loud
underwater would have the same
approximate effective intensity as a
sound that is 98.5 dB loud in air.
Sound frequency is measured in
cycles per second, or Hertz (abbreviated
Hz), and is analogous to musical pitch;
high-pitched sounds contain high
frequencies and low-pitched sounds
contain low frequencies. Natural sounds
in the ocean span a huge range of
frequencies: from earthquake noise at 5
Hz to harbor porpoise clicks at 150,000
Hz (150 kHz). These sounds are so low
or so high in pitch that humans cannot
even hear them; acousticians call these
infrasonic and ultrasonic sounds,
respectively. A single sound may be
made up of many different frequencies
together. Sounds made up of only a
small range of frequencies are called
‘‘narrowband’’, and sounds with a broad
range of frequencies are called
‘‘broadband’’; airguns are an example of
a broadband sound source and tactical
sonars are an example of a narrowband
sound source.
When considering the influence of
various kinds of sound on the marine
environment, it is necessary to
understand that different kinds of
marine life are sensitive to different
frequencies of sound. Based on available
behavioral data, audiograms derived
using auditory evoked potential,
anatomical modeling, and other data,
Southall et al. (2007) designated
‘‘functional hearing groups’’ and
estimated the lower and upper
frequencies of functional hearing of the
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groups. Further, the frequency range in
which each group’s hearing is estimated
as being most sensitive is represented in
the flat part of the M-weighting
functions developed for each group. The
functional groups and the associated
frequencies are indicated below:
• Low frequency cetaceans (13
species of mysticetes): Functional
hearing is estimated to occur between
approximately 7 Hz and 22 kHz.
• Mid-frequency cetaceans (32
species of dolphins, six species of larger
toothed whales, and 19 species of
beaked and bottlenose whales):
Functional hearing is estimated to occur
between approximately 150 Hz and 160
kHz.
• High frequency cetaceans (eight
species of true porpoises, six species of
river dolphins, Kogia, the franciscana,
and four species of cephalorhynchids):
Functional hearing is estimated to occur
between approximately 200 Hz and 180
kHz.
• Pinnipeds in Water: Functional
hearing is estimated to occur between
approximately 75 Hz and 75 kHz, with
the greatest sensitivity between
approximately 700 Hz and 20 kHz.
• Pinnipeds in Air: Functional
hearing is estimated to occur between
approximately 75 Hz and 30 kHz.
Because ears adapted to function
underwater are physiologically different
from human ears, comparisons using
decibel measurements in air would still
not be adequate to describe the effects
of a sound on a cetacean. When sound
travels away from its source, its
loudness decreases as the distance from
the source increases (propagation).
Thus, the loudness of a sound at its
source is higher than the loudness of
that same sound a kilometer distant.
Acousticians often refer to the loudness
of a sound at its source (typically
measured one meter from the source) as
the source level and the loudness of
sound elsewhere as the received level.
For example, a humpback whale three
kilometers from an airgun that has a
source level of 230 dB may only be
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exposed to sound that is 160 dB loud,
depending on how the sound
propagates. As a result, it is important
not to confuse source levels and
received levels when discussing the
loudness of sound in the ocean.
As sound travels from a source, its
propagation in water is influenced by
various physical characteristics,
including water temperature, depth,
salinity, and surface and bottom
properties that cause refraction,
reflection, absorption, and scattering of
sound waves. Oceans are not
homogeneous and the contribution of
each of these individual factors is
extremely complex and interrelated.
The physical characteristics that
determine the sound’s speed through
the water will change with depth,
season, geographic location, and with
time of day (as a result, in actual sonar
operations, crews will measure oceanic
conditions, such as sea water
temperature and depth, to calibrate
models that determine the path the
sonar signal will take as it travels
through the ocean and how strong the
sound signal will be at a given range
along a particular transmission path). As
sound travels through the ocean, the
intensity associated with the wavefront
diminishes, or attenuates. This decrease
in intensity is referred to as propagation
loss, also commonly called transmission
loss.
Metrics Used in This Document
This section includes a brief
explanation of the two sound
measurements (sound pressure level
(SPL) and sound exposure level (SEL))
frequently used in the discussions of
acoustic effects in this document.
SPL
Sound pressure is the sound force per
unit area, and is usually measured in
microPa, where 1 Pa is the pressure
resulting from a force of one newton
exerted over an area of one square
meter. SPL is expressed as the ratio of
a measured sound pressure and a
reference level. The commonly used
reference pressure level in underwater
acoustics is 1 microPa, and the units for
SPLs are dB re: 1 microPa.
SPL (in dB) = 20 log (pressure/
reference pressure)
SPL is an instantaneous measurement
and can be expressed as the peak, the
peak-peak, or the root mean square
(rms). Root mean square, which is the
square root of the arithmetic average of
the squared instantaneous pressure
values, is typically used in discussions
of the effects of sounds on vertebrates.
All references to SPL in this document
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refer to the root mean square. SPL does
not take the duration of a sound into
account. SPL is the applicable metric
used in the risk continuum, which is
used to estimate behavioral harassment
takes (see Level B Harassment Risk
Function (Behavioral Harassment)
Section).
SEL
SEL is an energy metric that integrates
the squared instantaneous sound
pressure over a stated time interval. The
units for SEL are dB re: 1 microPa2-s.
SEL = SPL + 10log (duration in seconds)
As applied to tactical sonar, the SEL
includes both the SPL of a sonar ping
and the total duration. Longer duration
pings and/or pings with higher SPLs
will have a higher SEL. Surface-ship
hull-mounted sonars, known as tactical
sonars, are not used by NAVSEA NUWC
Keyport. If an animal is exposed to
multiple pings, the SEL in each
individual ping is summed to calculate
the total SEL. The total SEL depends on
the SPL, duration, and number of pings
received. The thresholds that NMFS
uses to indicate the received levels at
which the onset of temporary threshold
shift (TTS) and permanent threshold
shift (PTS) in hearing are likely to occur
are expressed in SEL.
Potential Impacts to Marine Mammal
Species
The following sections discuss the
potential effects from noise related to
active acoustic devices that would be
used in the proposed Keyport Range
Complex Extension.
For activities involving active
acoustic sources such as tactical sonar,
NMFS’s analysis identifies the
probability of lethal responses, physical
trauma, sensory impairment (permanent
and temporary threshold shifts and
acoustic masking), physiological
responses (particular stress responses),
behavioral disturbance (that rises to the
level of harassment), and social
responses that would be classified as
behavioral harassment or injury and/or
would be likely to adversely affect the
species or stock through effects on
annual rates of recruitment or survival.
It should be noted that the description
below is based on more powerful midfrequency active sonar (MFAS) used on
surface ships. The NAVSEA NUWC
Keyport Range does not utilize these
sources in RDT&E activities. Many of
these severe effects (e.g., mortality,
acoustically mediated bubble growth,
and stranding) are not likely to occur for
acoustic sources used in the proposed
Keyport Range activities, as shown in
Estimated Takes of Marine Mammals
section.
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Direct Physiological Effects
Based on the literature, there are two
basic ways that MFAS might directly
result in physical trauma or damage:
Noise-induced loss of hearing
sensitivity (more commonly-called
‘‘threshold shift’’) and acoustically
mediated bubble growth. Separately, an
animal’s behavioral reaction to an
acoustic exposure might lead to
physiological effects that might
ultimately lead to injury or death, which
is discussed later in the Stranding
section.
Threshold Shift (Noise-Induced Loss of
Hearing)
When animals exhibit reduced
hearing sensitivity (i.e., sounds must be
louder for an animal to recognize them)
following exposure to a sufficiently
intense sound, it is referred to as a
noise-induced threshold shift (TS). An
animal can experience temporary
threshold shift (TTS) or permanent
threshold shift (PTS). TTS can last from
minutes or hours to days (i.e., there is
recovery), occurs in specific frequency
ranges (i.e., an animal might only have
a temporary loss of hearing sensitivity
between the frequencies of 1 and 10
kHz)), and can be of varying amounts
(for example, an animal’s hearing
sensitivity might be reduced by only 6
dB or reduced by 30 dB). PTS is
permanent (i.e., there is no recovery),
but as with TTS occurs in a specific
frequency range and amount.
The following physiological
mechanisms are thought to play a role
in inducing auditory TSs: Effects to
sensory hair cells in the inner ear that
reduce their sensitivity, modification of
the chemical environment within the
sensory cells, residual muscular activity
in the middle ear, displacement of
certain inner ear membranes, increased
blood flow, and post-stimulatory
reduction in both efferent and sensory
neural output (Southall et al., 2007).
The amplitude, duration, frequency,
temporal pattern, and energy
distribution of sound exposure all affect
the amount of associated TS and the
frequency range in which it occurs. As
amplitude and duration of sound
exposure increase, so, generally, does
the amount of TS. For continuous
sounds, exposures of equal energy (the
same SEL) will lead to approximately
equal effects. For intermittent sounds,
less TS will occur than from a
continuous exposure with the same
energy (some recovery will occur
between exposures) (Kryter et al., 1966;
Ward, 1997). For example, one short but
loud (higher SPL) sound exposure may
induce the same impairment as one
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longer but softer sound, which in turn
may cause more impairment than a
series of several intermittent softer
sounds with the same total energy
(Ward, 1997). Additionally, though TTS
is temporary, very prolonged exposure
to sound strong enough to elicit TTS, or
shorter-term exposure to sound levels
well above the TTS threshold, can cause
PTS, at least in terrestrial mammals
(Kryter, 1985) (although in the case of
MFAS, animals are not expected to be
exposed to levels high enough or
durations long enough to result in PTS).
PTS is considered auditory injury
(Southall et al., 2007). Irreparable
damage to the inner or outer cochlear
hair cells may cause PTS, however,
other mechanisms are also involved,
such as exceeding the elastic limits of
certain tissues and membranes in the
middle and inner ears and resultant
changes in the chemical composition of
the inner ear fluids (Southall et al.,
2007).
Although the published body of
scientific literature contains numerous
theoretical studies and discussion
papers on hearing impairments that can
occur with exposure to a loud sound,
only a few studies provide empirical
information on the levels at which
noise-induced loss in hearing sensitivity
occurs in nonhuman animals. For
cetaceans, published data are limited to
a captive bottlenose dolphin and beluga
whale (Finneran et al., 2000, 2002b,
2005a; Schlundt et al., 2000; Nachtigall
et al., 2003, 2004).
Marine mammal hearing plays a
critical role in communication with
conspecific, and interpreting
environmental cues for purposes such
as predator avoidance and prey capture.
Depending on the frequency range of
TTS degree (dB), duration, and
frequency range of TTS, and the context
in which it is experienced, TTS can
have effects on marine mammals
ranging from discountable to serious
(similar to those discussed in auditory
masking, below). For example, a marine
mammal may be able to readily
compensate for a brief, relatively small
amount of TTS in a non-critical
frequency range that takes place during
a time when the animal is traveling
through the open ocean, where ambient
noise is lower and there are not as many
competing sounds present.
Alternatively, a larger amount and
longer duration of TTS sustained during
time when communication is critical for
successful mother/calf interactions
could have more serious impacts. Also,
depending on the degree and frequency
range, the effects of PTS on an animal
could range in severity, although it is
considered generally more serious
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because it is a long term condition. Of
note, reduced hearing sensitivity as a
simple function of development and
aging has been observed in marine
mammals, as well as humans and other
taxa (Southall et al., 2007), so we can
infer that strategies exist for coping with
this condition to some degree, though
likely not without cost. There is no
empirical evidence that exposure to
MFAS can cause PTS in any marine
mammals; instead the probability of
PTS has been inferred from studies of
TTS (see Richardson et al., 1995).
Acoustically Mediated Bubble Growth
One theoretical cause of injury to
marine mammals is rectified diffusion
(Crum and Mao, 1996), the process of
increasing the size of a bubble by
exposing it to a sound field. This
process could be facilitated if the
environment in which the ensonified
bubbles exist is supersaturated with gas.
Repetitive diving by marine mammals
can cause the blood and some tissues to
accumulate gas to a greater degree than
is supported by the surrounding
environmental pressure (Ridgway and
Howard, 1979). The deeper and longer
dives of some marine mammals (for
example, beaked whales) are
theoretically predicted to induce greater
supersaturation (Houser et al., 2001b). If
rectified diffusion were possible in
marine mammals exposed to high-level
sound, conditions of tissue
supersaturation could theoretically
speed the rate and increase the size of
bubble growth. Subsequent effects due
to tissue trauma and emboli would
presumably mirror those observed in
humans suffering from decompression
sickness.
It is unlikely that the short duration
of sonar pings would be long enough to
drive bubble growth to any substantial
size, if such a phenomenon occurs.
Recent work conducted by Crum et al.
(2005) demonstrated the possibility of
rectified diffusion for short duration
signals, but at sound exposure levels
and tissue saturation levels that are
improbable to occur in a diving marine
mammal. However, an alternative but
related hypothesis has also been
suggested: Stable bubbles could be
destabilized by high-level sound
exposures such that bubble growth then
occurs through static diffusion of gas
out of the tissues. In such a scenario the
marine mammal would need to be in a
gas-supersaturated state for a long
enough period of time for bubbles to
become of a problematic size. Yet
another hypothesis (decompression
sickness) has speculated that rapid
ascent to the surface following exposure
to a startling sound might produce
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tissue gas saturation sufficient for the
evolution of nitrogen bubbles (Jepson et
al., 2003; Fernandez et al., 2005). In this
scenario, the rate of ascent would need
to be sufficiently rapid to compromise
behavioral or physiological protections
against nitrogen bubble formation.
Collectively, these hypotheses can be
referred to as ‘‘hypotheses of
acoustically mediated bubble growth.’’
Although theoretical predictions
suggest the possibility for acoustically
mediated bubble growth, there is
considerable disagreement among
scientists as to its likelihood (Piantadosi
and Thalmann, 2004; Evans and Miller,
2003). Crum and Mao (1996)
hypothesized that received levels would
have to exceed 190 dB in order for there
to be the possibility of significant
bubble growth due to supersaturation of
gases in the blood (i.e., rectified
diffusion). More recent work conducted
by Crum et al. (2005) demonstrated the
possibility of rectified diffusion for
short duration signals, but at SELs and
tissue saturation levels that are highly
improbable to occur in diving marine
mammals. To date, Energy Levels (ELs)
predicted to cause in vivo bubble
formation within diving cetaceans have
not been evaluated (NOAA, 2002b).
Although it has been argued that
traumas from some recent beaked whale
strandings are consistent with gas
emboli and bubble-induced tissue
separations (Jepson et al., 2003), there is
no conclusive evidence of this.
However, Jepson et al. (2003, 2005) and
Fernandez et al. (2004, 2005) concluded
that in vivo bubble formation, which
may be exacerbated by deep, long
duration, repetitive dives may explain
why beaked whales appear to be
particularly vulnerable to sonar
exposures. Further investigation is
needed to further assess the potential
validity of these hypotheses. More
information regarding hypotheses that
attempt to explain how behavioral
responses to MFAS can lead to
strandings is included in the
Behaviorally Mediated Bubble Growth
section, after the summary of strandings.
Acoustic Masking
Marine mammals use acoustic signals
for a variety of purposes, which differ
among species, but include
communication between individuals,
navigation, foraging, reproduction, and
learning about their environment (Erbe
and Farmer, 2000; Tyack, 2000).
Masking, or auditory interference,
generally occurs when sounds in the
environment are louder than and of a
similar frequency to, auditory signals an
animal is trying to receive. Masking is
a phenomenon that affects animals that
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are trying to receive acoustic
information about their environment,
including sounds from other members
of their species, predators, prey, and
sounds that allow them to orient in their
environment. Masking these acoustic
signals can disturb the behavior of
individual animals, groups of animals,
or entire populations.
The extent of the masking interference
depends on the spectral, temporal, and
spatial relationships between the signals
an animal is trying to receive and the
masking noise, in addition to other
factors. In humans, significant masking
of tonal signals occurs as a result of
exposure to noise in a narrow band of
similar frequencies. As the sound level
increases, though, the detection of
frequencies above those of the masking
stimulus decreases also. This principle
is expected to apply to marine mammals
as well because of common
biomechanical cochlear properties
across taxa.
Richardson et al. (1995) argued that
the maximum radius of influence of an
industrial noise (including broadband
low frequency sound transmission) on a
marine mammal is the distance from the
source to the point at which the noise
can barely be heard. This range is
determined by either the hearing
sensitivity of the animal or the
background noise level present.
Industrial masking is most likely to
affect some species’ ability to detect
communication calls and natural
sounds (i.e., surf noise, prey noise, etc.;
Richardson et al., 1995).
The echolocation calls of odontocetes
(toothed whales) are subject to masking
by high frequency sound. Human data
indicate low frequency sound can mask
high frequency sounds (i.e., upward
masking). Studies on captive
odontocetes by Au et al. (1974, 1985,
1993) indicate that some species may
use various processes to reduce masking
effects (e.g., adjustments in echolocation
call intensity or frequency as a function
of background noise conditions). There
is also evidence that the directional
hearing abilities of odontocetes are
useful in reducing masking at the high
frequencies these cetaceans use to
echolocate, but not at the low-to
moderate frequencies they use to
communicate (Zaitseva et al., 1980).
As mentioned previously, the
functional hearing ranges of marine
mammals all encompass the frequencies
of the active acoustic sources used in
the Navy’s Keyport Range activities.
Additionally, almost all species’ vocal
repertoires span across the frequencies
of the sources used by the Navy. The
closer the characteristics of the masking
signal to the signal of interest, the more
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likely masking is to occur. However,
because the pulse length and duty cycle
of source signals are of short duration
and would not be continuous, masking
is unlikely to occur as a result of
exposure to active acoustic sources
during the RDT&E activities in the
Keyport Range Complex Extension
Study Area.
Impaired Communication
In addition to making it more difficult
for animals to perceive acoustic cues in
their environment, anthropogenic sound
presents separate challenges for animals
that are vocalizing. When they vocalize,
animals are aware of environmental
conditions that affect the ‘‘active space’’
of their vocalizations, which is the
maximum area within which their
vocalizations can be detected before it
drops to the level of ambient noise
(Brenowitz, 2004; Brumm et al., 2004;
Lohr et al., 2003). Animals are also
aware of environmental conditions that
affect whether listeners can discriminate
and recognize their vocalizations from
other sounds, which are more important
than detecting a vocalization
(Brenowitz, 1982; Brumm et al., 2004;
Dooling, 2004; Marten and Marler, 1977;
Patricelli et al., 2006). Most animals that
vocalize have evolved an ability to make
adjustments to their vocalizations to
increase the signal-to-noise ratio, active
space, and recognizability of their
vocalizations in the face of temporary
changes in background noise (Brumm et
al., 2004; Patricelli et al., 2006).
Vocalizing animals will make one or
more of the following adjustments to
their vocalizations: Adjust the frequency
structure; adjust the amplitude; adjust
temporal structure; or adjust temporal
delivery.
Many animals will combine several of
these strategies to compensate for high
levels of background noise.
Anthropogenic sounds that reduce the
signal-to-noise ratio of animal
vocalizations, increase the masked
auditory thresholds of animals listening
for such vocalizations, or reduce the
active space of an animal’s vocalizations
impair communication between
animals. Most animals that vocalize
have evolved strategies to compensate
for the effects of short-term or temporary
increases in background or ambient
noise on their songs or calls. Although
the fitness consequences of these vocal
adjustments remain unknown, like most
other trade-offs animals must make,
some of these strategies probably come
at a cost (Patricelli et al., 2006). For
example, vocalizing more loudly in
noisy environments may have energetic
costs that decrease the net benefits of
vocal adjustment and alter a bird’s
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energy budget (Brumm, 2004; Wood and
Yezerinac, 2006). Shifting songs and
calls to higher frequencies may also
impose energetic costs (Lambrechts,
1996).
Stress Responses
Classic stress responses begin when
an animal’s central nervous system
perceives a potential threat to its
homeostasis. That perception triggers
stress responses regardless of whether a
stimulus actually threatens the animal;
the mere perception of a threat is
sufficient to trigger a stress response
(Moberg, 2000; Sapolsky et al., 2005;
Seyle, 1950). Once an animal’s central
nervous system perceives a threat, it
mounts a biological response or defense
that consists of a combination of the
four general biological defense
responses: Behavioral responses,
autonomic nervous system responses,
neuroendocrine responses, or immune
response.
In the case of many stressors, an
animal’s first and most economical (in
terms of biotic costs) response is
behavioral avoidance of the potential
stressor or avoidance of continued
exposure to a stressor. An animal’s
second line of defense to stressors
involves the autonomic nervous system
and the classical ‘‘fight or flight’’
response which includes the
cardiovascular system, the
gastrointestinal system, the exocrine
glands, and the adrenal medulla to
produce changes in heart rate, blood
pressure, and gastrointestinal activity
that humans commonly associate with
‘‘stress.’’ These responses have a
relatively short duration and may or
may not have significant long-term
effects on an animal’s welfare.
An animal’s third line of defense to
stressors involves its neuroendocrine or
sympathetic nervous systems; the
system that has received the most study
has been the hypothalmus-pituitaryadrenal system (also known as the HPA
axis in mammals or the hypothalamuspituitary-interrenal axis in fish and
some reptiles). Unlike stress responses
associated with the autonomic nervous
system, virtually all neuro-endocrine
functions that are affected by stress—
including immune competence,
reproduction, metabolism, and
behavior—are regulated by pituitary
hormones. Stress-induced changes in
the secretion of pituitary hormones have
been implicated in failed reproduction
(Moberg, 1987; Rivier, 1995) and altered
metabolism (Elasser et al., 2000),
reduced immune competence (Blecha,
2000) and behavioral disturbance.
Increases in the circulation of
glucocorticosteroids (cortisol,
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corticosterone, and aldosterone in
marine mammals; Romano et al., 2004)
have been equated with stress for many
years.
The primary distinction between
stress (which is adaptive and does not
normally place an animal at risk) and
distress is the biotic cost of the
response. During a stress response, an
animal uses glycogen stores that can be
quickly replenished once the stress is
alleviated. In such circumstances, the
cost of the stress response would not
pose a risk to the animal’s welfare.
However, when an animal does not have
sufficient energy reserves to satisfy the
energetic costs of a stress response,
energy resources must be diverted from
other biotic functions, which impair
those functions that experience the
diversion. For example, when mounting
a stress response diverts energy away
from growth in young animals, those
animals may experience stunted growth.
When mounting a stress response
diverts energy from a fetus, an animal’s
reproductive success and its fitness will
suffer. In these cases, the animals will
have entered a pre-pathological or
pathological state which is called
‘‘distress’’ (sensu Seyle, 1950) or
‘‘allostatic loading’’ (sensu McEwen and
Wingfield, 2003). This pathological state
will last until the animal replenishes its
biotic reserves sufficient to restore
normal function.
Relationships between these
physiological mechanisms, animal
behavior, and the costs of stress
responses have also been documented
fairly well through controlled
experiments; because this physiology
exists in every vertebrate that has been
studied, it is not surprising that stress
responses and their costs have been
documented in both laboratory and freeliving animals (for examples see,
Holberton et al., 1996; Hood et al., 1998;
Jessop et al., 2003; Krausman et al.,
2004; Lankford et al., 2005; Reneerkens
et al., 2002; Thompson and Hamer,
2000). Although no information has
been collected on the physiological
responses of marine mammals to
exposure to anthropogenic sounds,
studies of other marine animals and
terrestrial animals would lead us to
expect some marine mammals to
experience physiological stress
responses and, perhaps, physiological
responses that would be classified as
‘‘distress’’ upon exposure to midfrequency and low frequency sounds.
For example, Jansen (1998) reported
on the relationship between acoustic
exposures and physiological responses
that are indicative of stress responses in
humans (for example, elevated
respiration and increased heart rates).
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Jones (1998) reported on reductions in
human performance when faced with
acute, repetitive exposures to acoustic
disturbance. Trimper et al. (1998)
reported on the physiological stress
responses of osprey to low-level aircraft
noise while Krausman et al. (2004)
reported on the auditory and physiology
stress responses of endangered Sonoran
pronghorn to military overflights. Smith
et al. (2004a, 2004b) identified noise
induced physiological transient stress
responses in hearing-specialist fish that
accompanied short- and long-term
hearing losses. Welch and Welch (1970)
reported physiological and behavioral
stress responses that accompanied
damage to the inner ears of fish and
several mammals.
Hearing is one of the primary senses
cetaceans use to gather information
about their environment and to
communicate with conspecifics.
Although empirical information on the
relationship between sensory
impairment (TTS, PTS, and acoustic
masking) on cetaceans remains limited,
it seems reasonable to assume that
reducing an animal’s ability to gather
information about its environment and
to communicate with other members of
its species would be stressful for
animals that use hearing as their
primary sensory mechanism. Therefore,
we assume that acoustic exposures
sufficient to trigger onset PTS or TTS
would be accompanied by physiological
stress responses because terrestrial
animals exhibit those responses under
similar conditions (NRC, 2003). More
importantly, marine mammals might
experience stress responses at received
levels lower than those necessary to
trigger onset TTS. Based on empirical
studies of the time required to recover
from stress responses (Moberg, 2000),
we also assume that stress responses are
likely to persist beyond the time interval
required for animals to recover from
TTS and might result in pathological
and pre-pathological states that would
be as significant as behavioral responses
to TTS.
Behavioral Disturbance
Behavioral responses to sound are
highly variable and context-specific.
Exposure of marine mammals to sound
sources can result in (but is not limited
to) the following observable responses:
Increased alertness; orientation or
attraction to a sound source; vocal
modifications; cessation of feeding;
cessation of social interaction; alteration
of movement or diving behavior; habitat
abandonment (temporary or permanent);
and, in severe cases, panic, flight,
stampede, or stranding, potentially
resulting in death (Southall et al., 2007).
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Many different variables can
influence an animal’s perception of and
response to (nature and magnitude) an
acoustic event. An animal’s prior
experience with a sound type affects
whether it is less likely (habituation) or
more likely (sensitization) to respond to
certain sounds in the future (animals
can also be innately pre-disposed to
respond to certain sounds in certain
ways) (Southall et al., 2007). Related to
the sound itself, the perceived nearness
of the sound, bearing of the sound
(approaching vs. retreating), similarity
of a sound to biologically relevant
sounds in the animal’s environment
(i.e., calls of predators, prey, or
conspecifics), and familiarity of the
sound may affect the way an animal
responds to the sound (Southall et al.,
2007). Individuals (of different age,
gender, reproductive status, etc.) among
most populations will have variable
hearing capabilities, and differing
behavioral sensitivities to sounds that
will be affected by prior conditioning,
experience, and current activities of
those individuals. Often, specific
acoustic features of the sound and
contextual variables (i.e., proximity,
duration, or recurrence of the sound or
the current behavior that the marine
mammal is engaged in or its prior
experience), as well as entirely separate
factors such as the physical presence of
a nearby vessel, may be more relevant
to the animal’s response than the
received level alone.
There are few empirical studies of
avoidance responses of free-living
cetaceans to mid-frequency sonars.
Much more information is available on
the avoidance responses of free-living
cetaceans to other acoustic sources, like
seismic airguns and low frequency
sonar, than mid-frequency active sonar.
Richardson et al., (1995) noted that
avoidance reactions are the most
obvious manifestations of disturbance in
marine mammals.
Behavioral Responses (Southall et al.
(2007))
Southall et al., (2007) reports the
results of the efforts of experts in
acoustic research from behavioral,
physiological, and physical disciplines
that convened and reviewed the
available literature on marine mammal
hearing and physiological and
behavioral responses to anthropogenic
sound with the goal of proposing
exposure criteria for certain effects. This
compilation of literature is very
valuable, though Southall et al. notes
that not all data is equal: Some have
poor statistical power, insufficient
controls, and/or limited information on
received levels, background noise, and
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other potentially important contextual
variables; such data were reviewed and
sometimes used for qualitative
illustration, but were not included in
the quantitative analysis for the criteria
recommendations.
In the Southall et al., (2007) report, for
the purposes of analyzing responses of
marine mammals to anthropogenic
sound and developing criteria, the
authors differentiate between single
pulse sounds, multiple pulse sounds,
and non-pulse sounds. Sonar signal is
considered a non-pulse sound. Southall
et al., (2007) summarize the reports
associated with low, mid, and high
frequency cetacean responses to nonpulse sounds in Appendix C of their
report (incorporated by reference and
summarized in the three paragraphs
below).
The reports that address responses of
low frequency cetaceans to non-pulse
sounds include data gathered in the
field and related to several types of
sound sources (of varying similarity to
sonar signals) including: Vessel noise,
drilling and machinery playback, low
frequency M-sequences (sine wave with
multiple phase reversals) playback, low
frequency active sonar playback, drill
vessels, Acoustic Thermometry of
Ocean Climate (ATOC) source, and nonpulse playbacks. These reports generally
indicate no (or very limited) responses
to received levels in the 90 to 120 dB
re 1 micro Pa range and an increasing
likelihood of avoidance and other
behavioral effects in the 120 to 160 dB
range. As mentioned earlier, however,
contextual variables play a very
important role in the reported
responses, and the severity of effects are
not linear when compared to received
level. Also, few of the laboratory or field
datasets had common conditions,
behavioral contexts or sound sources, so
it is not surprising that responses differ.
The reports that address responses of
mid-frequency cetaceans to non-pulse
sounds include data gathered both in
the field and the laboratory and related
to several different sound sources (of
varying similarity to sonar signals)
including: Pingers, drilling playbacks,
vessel and ice-breaking noise, vessel
noise, Acoustic Harassment Devices
(AHDs), Acoustic Deterrent Devices
(ADDs), HFAS/MFAS, and non-pulse
bands and tones. Southall et al. were
unable to come to a clear conclusion
regarding these reports. In some cases,
animals in the field showed significant
responses to received levels between 90
and 120 dB, while in other cases these
responses were not seen in the 120 to
150 dB range. The disparity in results
was likely due to contextual variation
and the differences between the results
in the field and laboratory data (animals
responded at lower levels in the field).
The reports that address the responses
of high frequency cetaceans to nonpulse sounds include data gathered both
in the field and the laboratory and
related to several different sound
sources (of varying similarity to sonar
signals) including: Acoustic harassment
devices, Acoustical Telemetry of Ocean
Climate (ATOC), wind turbine, vessel
noise, and construction noise. However,
no conclusive results are available from
these reports. In some cases, high
frequency cetaceans (harbor porpoises)
are observed to be quite sensitive to a
wide range of human sounds at very low
exposure RLs (90 to 120 dB). All
recorded exposures exceeding 140 dB
produced profound and sustained
avoidance behavior in wild harbor
porpoises (Southall et al., 2007).
In addition to summarizing the
available data, the authors of Southall et
al. (2007) developed a severity scaling
system with the intent of ultimately
being able to assign some level of
biological significance to a response.
Following is a summary of their scoring
system: A comprehensive list of the
behaviors associated with each score
may be found in the report:
• 0–3 (Minor and/or brief behaviors)
includes, but is not limited to: No
response; minor changes in speed or
locomotion (but with no avoidance);
individual alert behavior; minor
cessation in vocal behavior; minor
changes in response to trained behaviors
(in laboratory).
• 4–6 (Behaviors with higher
potential to affect foraging,
reproduction, or survival) includes, but
is not limited to: Moderate changes in
speed, direction, or dive profile; brief
shift in group distribution; prolonged
cessation or modification of vocal
behavior (duration > duration of sound),
minor or moderate individual and/or
group avoidance of sound; brief
cessation of reproductive behavior; or
refusal to initiate trained tasks (in
laboratory).
• 7–9 (Behaviors considered likely to
affect the aforementioned vital rates)
includes, but are not limited to:
Extensive of prolonged aggressive
behavior; moderate, prolonged or
significant separation of females and
dependent offspring with disruption of
acoustic reunion mechanisms; long-term
avoidance of an area; outright panic,
stampede, stranding; threatening or
attacking sound source (in laboratory).
In Table 7 we have summarized the
scores that Southall et al. (2007)
assigned to the papers that reported
behavioral responses of low frequency
cetaceans, mid-frequency cetaceans, and
high frequency cetaceans to non-pulse
sounds.
TABLE 7—DATA COMPILED FROM THREE TABLES FROM SOUTHALL ET AL. (2007) INDICATING WHEN MARINE MAMMALS
(LOW-FREQUENCY CETACEAN = L, MID-FREQUENCY CETACEAN = M, AND HIGH-FREQUENCY CETACEAN = H) WERE
REPORTED AS HAVING A BEHAVIORAL RESPONSE OF THE INDICATED SEVERITY TO A NON-PULSE SOUND OF THE INDICATED RECEIVED LEVEL
[As discussed in the text, responses are highly variable and context specific]
Response Score
Received RMS sound pressure
level (dB re 1 microPa)
9
8
7
6
5
4
3
2
1
0
................................................
................................................
................................................
................................................
................................................
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100
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110
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<120
120 to <
130
130 to <
140
140 to <
150
150 to <
160
160 to <
170
170 to <
180
180 to <
190
190 to <
200
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Potential Effects of Behavioral
Disturbance
The different ways that marine
mammals respond to sound are
sometimes indicators of the ultimate
effect that exposure to a given stimulus
will have on the well-being (survival,
reproduction, etc.) of an animal. There
is little marine mammal data
quantitatively relating the exposure of
marine mammals to sound to effects on
reproduction or survival, though data
exist for terrestrial species from which
we can draw comparisons for marine
mammals.
Attention is the cognitive process of
selectively concentrating on one aspect
of an animal’s environment while
ignoring other things (Posner, 1994).
Because animals (including humans)
have limited cognitive resources, there
is a limit to how much sensory
information they can process at any
time. The phenomenon called
‘‘attentional capture’’ occurs when a
stimulus (such as a stimulus that an
animal is not concentrating on or
attending to) ‘‘captures’’ an animal’s
attention. This shift in attention can
occur consciously or unconsciously (for
example, when an animal hears sounds
that it associates with the approach of
a predator) and the shift in attention can
be sudden (Dukas, 2002; van Rij, 2007).
Once a stimulus has captured an
animal’s attention, the animal can
respond by ignoring the stimulus,
assuming a ‘‘watch and wait’’ posture,
or treat the stimulus as a disturbance
and respond accordingly, which
includes scanning for the source of the
stimulus or ‘‘vigilance’’ (Cowlishaw et
al., 2004).
Vigilance is normally an adaptive
behavior that helps animals determine
the presence or absence of predators,
assess their distance from conspecifics,
or to attend cues from prey (Bednekoff
and Lima, 1998; Treves, 2000). Despite
those benefits, however, vigilance has a
cost of time: When animals focus their
attention on specific environmental
cues, they are not attending to other
activities such as foraging. These costs
have been documented best in foraging
animals, where vigilance has been
shown to substantially reduce feeding
rates (Saino, 1994; Beauchamp and
Livoreil, 1997; Fritz et al., 2002).
Animals will spend more time being
vigilant, which may translate to less
time foraging or resting, when
disturbance stimuli approach them
more directly, remain at closer
distances, have a greater group size (for
example, multiple surface vessels), or
when they co-occur with times that an
animal perceives increased risk (for
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example, when they are giving birth or
accompanied by a calf). Most of the
published literature, however, suggests
that direct approaches will increase the
amount of time animals will dedicate to
being vigilant. For example, bighorn
sheep and Dall’s sheep dedicated more
time being vigilant, and less time resting
or foraging, when aircraft made direct
approaches over them (Frid, 2001;
Stockwell et al., 1991).
Several authors have established that
long-term and intense disturbance
stimuli can cause population declines
by reducing the body condition of
individuals that have been disturbed,
followed by reduced reproductive
success, reduced survival, or both (Daan
et al., 1996; Madsen, 1994; White,
1983). For example, Madsen (1994)
reported that pink-footed geese (Anser
brachyrhynchus) in undisturbed habitat
gained body mass and had about a 46percent reproductive success compared
with geese in disturbed habitat (being
consistently scared off the fields on
which they were foraging) which did
not gain mass and had a 17 percent
reproductive success. Similar
reductions in reproductive success have
been reported for mule deer (Odocoileus
hemionus) disturbed by all-terrain
vehicles (Yarmoloy et al., 1988), caribou
disturbed by seismic exploration blasts
(Bradshaw et al., 1998), caribou
disturbed by low-elevation military
jetfights (Luick et al., 1996), and caribou
disturbed by low-elevation jet flights
(Harrington and Veitch, 1992).
Similarly, a study of elk (Cervus
elaphus) that were disturbed
experimentally by pedestrians
concluded that the ratio of young to
mothers was inversely related to
disturbance rate (Phillips and
Alldredge, 2000).
The primary mechanism by which
increased vigilance and disturbance
appear to affect the fitness of individual
animals is by disrupting an animal’s
time budget and, as a result, reducing
the time they might spend foraging and
resting (which increases an animal’s
activity rate and energy demand). For
example, a study of grizzly bears (Ursus
horribilis) reported that bears disturbed
by hikers reduced their energy intake by
an average of 12 kcal/min (50.2 × 103 kJ/
min), and spent energy fleeing or acting
aggressively toward hikers (White et al.,
1999).
On a related note, many animals
perform vital functions, such as feeding,
resting, traveling, and socializing, on a
diel cycle (24-hr cycle). Substantive
behavioral reactions to noise exposure
(such as disruption of critical life
functions, displacement, or avoidance of
important habitat) are more likely to be
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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).
Stranding and Mortality
When a live or dead marine mammal
swims or floats onto shore and becomes
‘‘beached’’ or incapable of returning to
sea, the event is termed a ‘‘stranding’’
(Geraci et al., 1999; Perrin and Geraci,
2002; Geraci and Lounsbury, 2005;
NMFS, 2007). The legal definition for a
stranding within the United States is
that ‘‘(A) a marine mammal is dead and
is (i) on a beach or shore of the United
States; or (ii) in waters under the
jurisdiction of the United States
(including any navigable waters); or (B)
a marine mammal is alive and is (i) on
a beach or shore of the United States
and is unable to return to the water; (ii)
on a beach or shore of the United States
and, although able to return to the
water, is in need of apparent medical
attention; or (iii) in the waters under the
jurisdiction of the United States
(including any navigable waters), but is
unable to return to its natural habitat
under its own power or without
assistance.’’ (16 U.S.C. 1421h).
Marine mammals are known to strand
for a variety of reasons, such as
infectious agents, biotoxicosis,
starvation, fishery interaction, ship
strike, unusual oceanographic or
weather events, sound exposure, or
combinations of these stressors
sustained concurrently or in series.
However, the cause or causes of most
stranding are unknown (Geraci et al.,
1976; Eaton, 1979, Odell et al., 1980;
Best, 1982). Numerous studies suggest
that the physiology, behavior, habitat
relationships, age, or condition of
cetaceans may cause them to strand or
might pre-dispose them to strand when
exposed to these phenomena. These
suggestions are consistent with the
conclusions of numerous other studies
that have demonstrated that
combinations of dissimilar stressors
commonly combine to kill an animal or
dramatically reduce its fitness, even
though one exposure without the other
does not produce the same result
(Chroussos, 2000; Creel, 2005; DeVries
et al., 2003; Fair and Becker, 2000; Foley
et al., 2001; Moberg, 2000; Relyea,
2005a; 2005b, Romero, 2004; Sih et al.,
2004).
Several sources have published lists
of mass stranding events of cetaceans
during attempts to identify relationships
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between those stranding events and
military sonar (Hildebrand, 2004; IWC,
2005; Taylor et al., 2004). For example,
based on a review of stranding records
between 1960 and 1995, the
International Whaling Commission
(IWC, 2005) identified ten mass
stranding events of Cuvier’s beaked
whales that had been reported and one
mass stranding of four Baird’s beaked
whales (Berardius bairdii). The IWC
concluded that, out of eight stranding
events reported from the mid-1980s to
the summer of 2003, seven had been
associated with the use of midfrequency sonar, one of those seven had
been associated with the use of low
frequency sonar, and the remaining
stranding event had been associated
with the use of seismic airguns.
Most of the stranding events reviewed
by the IWC involved beaked whales. A
mass stranding of Cuvier’s beaked
whales in the eastern Mediterranean Sea
occurred in 1996 (Frantzis, 1998) and
mass stranding events involving
Gervais’ beaked whales, Blainville’s
beaked whales, and Cuvier’s beaked
whales occurred off the coast of the
Canary Islands in the late 1980s
(Simmonds and Lopez-Jurado, 1991).
The stranding events that occurred in
the Canary Islands and Kyparissiakos
Gulf in the late 1990s and the Bahamas
in 2000 have been the most intensively
studied mass stranding events and have
been associated with naval maneuvers
that were using sonar.
Between 1960 and 2006, 48 strandings
(68 percent) involved beaked whales, 3
(4 percent) involved dolphins, and 14
(20 percent) involved other whale
species. Cuvier’s beaked whales were
involved in the greatest number of these
events (48 strandings or 68 percent),
followed by sperm whales (7 strandings
or 10 percent), and Blainville’s and
Gervais’ beaked whales (4 each or 6
percent). Naval activities that might
have involved active sonar are reported
to have coincided with 9 (13 percent) or
10 (14 percent) of those stranding
events. Between the mid-1980s and
2003 (the period reported by the IWC),
we identified reports of 44 mass
cetacean stranding events of which at
least 7 were coincident with naval
exercises that were using mid-frequency
sonar. A list of stranding events that are
considered to be associated with MFAS
is presented in the proposed rulemaking
for the Navy’s training in the Hawaii
Range Complex (73 FR 35510; June 23,
2008).
Association Between Mass Stranding
Events and Exposure to MFAS
Several authors have noted
similarities between some of these mass
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stranding incidents: They occurred in
islands or archipelagoes with deep
water nearby, several appeared to have
been associated with acoustic
waveguides like surface ducting, and
the sound fields created by vessels
transmitting mid-frequency sonar (Cox
et al., 2006, D’Spain et al., 2006).
However, only low intensity sonars and
low intensity acoustic sources are
proposed for the Keyport Range
Complex RDT&E and range extension
activities, and no powerful MFAS such
as the 53C series tactical sonar would be
used for these activities; therefore, their
zones of influence are much smaller
compared to these highest powered
surface vessel sources, and animals can
be more easily detected in these smaller
areas, thereby increasing the probability
that sonar operations can be modified to
reduce the risk of injury to marine
mammals. In addition, the proposed test
events differ significantly from major
Navy exercises and training, which
involve multi-vessel training scenarios
using the AN/SQS–53/56 source that
have been associated with past
strandings. Therefore, their zones of
influence are much smaller and are less
likely to affect marine mammals.
Although Cuvier’s beaked whales have
been the most common species involved
in these stranding events (81 percent of
the total number of stranded animals),
other beaked whales (including
Mesoplodon europeaus, M. densirostris,
and Hyperoodon ampullatus) comprise
14 percent of the total. Other species
(Stenella coeruleoalba, Kogia breviceps
and Balaenoptera acutorostrata) have
stranded, but in much lower numbers
and less consistently than beaked
whales.
Based on the available evidence,
however, we cannot determine whether
(a) Cuvier’s beaked whale is more prone
to injury from high-intensity sound than
other species, (b) their behavioral
responses to sound make them more
likely to strand, or (c) they are more
likely to be exposed to mid-frequency
active sonar than other cetaceans (for
reasons that remain unknown). Because
the association between active sonar
(mid-frequency) exposures and marine
mammal mass stranding events is not
consistent—some marine mammals
strand without being exposed to sonar
and some sonar transmissions are not
associated with marine mammal
stranding events despite their cooccurrence—other risk factors or a
grouping of risk factors probably
contribute to these stranding events.
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Behaviorally Mediated Responses to
HFAS/MFAS That May Lead to
Stranding
Although the confluence of Navy midfrequency active tactical sonar with the
other contributory factors noted in the
report was identified as the cause of the
2000 Bahamas stranding event, the
specific mechanisms that led to that
stranding (or the others) are not
understood, and there is uncertainty
regarding the ordering of effects that led
to the stranding. It is unclear whether
beaked whales were directly injured by
sound (acoustically mediated bubble
growth, addressed above) prior to
stranding or whether a behavioral
response to sound occurred that
ultimately caused the beaked whales to
strand and be injured.
Although causal relationships
between beaked whale stranding events
and active sonar remain unknown,
several authors have hypothesized that
stranding events involving these species
in the Bahamas and Canary Islands may
have been triggered when the whales
changed their dive behavior in a startle
response to exposure to active sonar or
to further avoid exposure (Cox et al.,
2006, Rommel et al., 2006). These
authors proposed three mechanisms by
which the behavioral responses of
beaked whales upon being exposed to
active sonar might result in a stranding
event. These include: Gas bubble
formation caused by excessively fast
surfacing; remaining at the surface too
long when tissues are supersaturated
with nitrogen; or diving prematurely
when extended time at the surface is
necessary to eliminate excess nitrogen.
More specifically, beaked whales that
occur in deep waters that are in close
proximity to shallow waters (for
example, the ‘‘canyon areas’’ that are
cited in the Bahamas stranding event;
see D’Spain and D’Amico, 2006), may
respond to active sonar by swimming
into shallow waters to avoid further
exposures and strand if they were not
able to swim back to deeper waters.
Second, beaked whales exposed to
active sonar might alter their dive
behavior. Changes in their dive behavior
might cause them to remain at the
surface or at depth for extended periods
of time, which could lead to hypoxia
directly by increasing their oxygen
demands or indirectly by increasing
their energy expenditures (to remain at
depth) and increase their oxygen
demands as a result. If beaked whales
are at depth when they detect a ping
from an active sonar transmission and
change their dive profile, this could lead
to the formation of significant gas
bubbles, which could damage multiple
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organs or interfere with normal
physiological function (Cox et al., 2006;
Rommel et al., 2006; Zimmer and
Tyack, 2007). Baird et al. (2005) found
that slow ascent rates from deep dives
and long periods of time spent within
50 m of the surface were typical for both
Cuvier’s and Blainville’s beaked whales,
the two species involved in mass
strandings related to naval sonar. These
two behavioral mechanisms may be
necessary to purge excessive dissolved
nitrogen concentrated in their tissues
during their frequent long dives (Baird
et al., 2005). Baird et al. (2005) further
suggests that abnormally rapid ascents
or premature dives in response to high
intensity sonar could indirectly result in
physical harm to the beaked whales,
through the mechanisms described
above (gas bubble formation or nonelimination of excess nitrogen).
Because many species of marine
mammals make repetitive and
prolonged dives to great depths, it has
long been assumed that marine
mammals have evolved physiological
mechanisms to protect against the
effects of rapid and repeated
decompressions. Although several
investigators have identified
physiological adaptations that may
protect marine mammals against
nitrogen gas supersaturation (alveolar
collapse and elective circulation;
Kooyman et al., 1972; Ridgway and
Howard, 1979), Ridgway and Howard
(1979) reported that bottlenose dolphins
that were trained to dive repeatedly had
muscle tissues that were substantially
supersaturated with nitrogen gas.
Houser et al. (2001) used these data to
model the accumulation of nitrogen gas
within the muscle tissue of other marine
mammal species and concluded that
cetaceans that dive deep and have slow
ascent or descent speeds would have
tissues that are more supersaturated
with nitrogen gas than other marine
mammals. Based on these data, Cox et
al. (2006) hypothesized that a critical
dive sequence might make beaked
whales more prone to stranding in
response to acoustic exposures. The
sequence began with (1) very deep (to
depths as deep as 2 kilometers) and long
(as long as 90 minutes) foraging dives
with (2) relatively slow, controlled
ascents, followed by (3) a series of
‘‘bounce’’ dives between 100 and 400 m
(328 and 1,323 ft) in depth (also see
Zimmer and Tyack, 2007). They
concluded that acoustic exposures that
disrupted any part of this dive sequence
(for example, causing beaked whales to
spend more time at surface without the
bounce dives that are necessary to
recover from the deep dive) could
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produce excessive levels of nitrogen
supersaturation in their tissues, leading
to gas bubble and emboli formation that
produces pathologies similar to
decompression sickness.
Recently, Zimmer and Tyack (2007)
modeled nitrogen tension and bubble
growth in several tissue compartments
for several hypothetical dive profiles
and concluded that repetitive shallow
dives (defined as a dive where depth
does not exceed the depth of alveolar
collapse, approximately 72 m (236 ft) for
Ziphius), perhaps as a consequence of
an extended avoidance reaction to sonar
sound, could pose a risk for
decompression sickness and that this
risk should increase with the duration
of the response. Their models also
suggested that unrealistically more
rapid ascent rates from normal dive
behaviors are unlikely to result in
supersaturation to the extent that bubble
formation would be expected. Tyack et
al. (2006) suggested that emboli
observed in animals exposed to
midfrequency range sonar (Jepson et al.,
2003; Fernandez et al., 2005) could stem
from a behavioral response that involves
repeated dives shallower than the depth
of lung collapse. Given that nitrogen gas
accumulation is a passive process (i.e.,
nitrogen is metabolically inert), a
bottlenose dolphin was trained to
repetitively dive a profile predicted to
elevate nitrogen saturation to the point
that nitrogen bubble formation was
predicted to occur. However, inspection
of the vascular system of the dolphin via
ultrasound did not demonstrate the
formation of asymptomatic nitrogen gas
bubbles (Houser et al., 2007).
If marine mammals respond to a Navy
vessel that is transmitting active sonar
in the same way that they might
respond to a predator, their probability
of flight responses should increase
when they perceive that Navy vessels
are approaching them directly, because
a direct approach may convey detection
and intent to capture (Burger and
Gochfeld, 1981; 1990; Cooper, 1997;
1998). The probability of flight
responses should also increase as
received levels of active sonar increase
(and the vessel is, therefore, closer) and
as vessel speeds increase (that is, as
approach speeds increase). For example,
the probability of flight responses in
Dall’s sheep (Ovis dalli dalli) (Frid,
2001a, b), ringed seals (Phoca hispida)
(Born et al., 1999), Pacific brant (Branta
bernic nigricans) and Canada geese (B.
canadensis) increased as a helicopter or
fixed-wing aircraft approached groups
of these animals more directly (Ward et
al., 1999). Bald eagles (Haliaeetus
leucocephalus) perched on trees
alongside a river were also more likely
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to flee from a paddle raft when their
perches were closer to the river or were
closer to the ground (Steidl and
Anthony, 1996).
Despite the many theories involving
bubble formation (both as a direct cause
of injury (see Acoustically Mediated
Bubble Growth Section) and an indirect
cause of stranding (see Behaviorally
Mediated Bubble Growth Section),
Southall et al., (2007) summarizes that
scientific disagreement or complete lack
of information exists regarding the
following important points: (1) Received
acoustical exposure conditions for
animals involved in stranding events;
(2) pathological interpretation of
observed lesions in stranded marine
mammals; (3) acoustic exposure
conditions required to induce such
physical trauma directly; (4) whether
noise exposure may cause behavioral
reactions (such as atypical diving
behavior) that secondarily cause bubble
formation and tissue damage; and (5)
the extent to which the post mortem
artifacts introduced by decomposition
before sampling, handling, freezing, or
necropsy procedures affect
interpretation of observed lesions.
Unlike those past stranding events
that were coincident with military midfrequency sonar use and were
speculated to most likely have been
caused by exposure to the sonar, those
naval exercises involved multiple
vessels in waters with steep bathymetry
where deep channeling of sonar signals
was more likely. The proposed RDT&E
activities within the Keyport Range
Complex Extension would not involve
multi-vessel operations, would not use
powerful sonar such as the AN/SQQ–
53C/56 MFAS, and the bathymetry bears
no similarity to where those mass
strandings occurred (e.g., Greece (1996);
the Bahamas (2000); Madeira (2000);
Canary Islands (2002); Hanalei Bay,
Kaua’i, Hawaii (2004); and Spain
(2006)). Consequently, because of the
nature of the Keyport Range operations
(which involve less powerful active
sonar (MFAS/HFAS) and other sound
sources, and no high-speed, multi-vessel
training scenarios) and the fact that the
Keyport Range Complex Extension has
none of the bathymetric features that
have been associated with mass
strandings in the past, NMFS concludes
it is unlikely that sonar use would result
in a stranding event in the Keyport
Range Complex region.
Estimated Take of Marine Mammals
With respect to the MMPA, NMFS’s
effects assessment serves four primary
purposes: (1) To prescribe the
permissible methods of taking (i.e.,
Level B Harassment (behavioral
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harassment), Level A harassment
(injury), or mortality, including an
identification of the number and types
of take that could occur by Level A or
B harassment or mortality) and to
prescribe other means of effecting the
least practicable adverse impact on such
species or stock and its habitat (i.e.,
mitigation); (2) to determine whether
the specified activity will have a
negligible impact on the affected species
or stocks of marine mammals (based on
the likelihood that the activity will
adversely affect the species or stock
through effects on annual rates of
recruitment or survival); (3) to
determine whether the specified activity
will have an unmitigable adverse impact
on the availability of the species or
stock(s) for subsistence uses (however,
there are no subsistence communities
that would be affected in the Keyport
Range Complex Study Area, so this
determination is inapplicable for this
rulemaking); and (4) to prescribe
requirements pertaining to monitoring
and reporting.
In the Potential Impacts to Marine
Mammal Species section, NMFS
identifies the lethal responses, physical
trauma, sensory impairment (permanent
and temporary threshold shifts and
acoustic masking), physiological
responses (particular stress responses),
and behavioral responses that could
potentially result from exposure to
active acoustic sources (e.g., powerful
sonar). In this section, we will relate the
potential effects to marine mammals
from active acoustic sources to the
MMPA regulatory definitions of Level A
and Level B Harassment and attempt to
quantify the effects that might occur
from the specific RDT&E activities that
the Navy is proposing in the Keyport
Range Complex.
Definition of Harassment
As mentioned previously, with
respect to military readiness activities,
Section 3(18)(B) of 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].
Level B Harassment
Of the potential effects that were
described in the Potential Impacts to
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Marine Mammals Species section, the
following are the types of effects that
fall into the Level B Harassment
category:
Behavioral Harassment—Behavioral
disturbance that rises to the level
described in the definition above, when
resulting from exposures to active
acoustic sources, is considered Level B
Harassment. Some of the lower level
physiological stress responses will also
likely co-occur with the predicted
harassments, although these responses
are more difficult to detect and fewer
data exist relating these responses to
specific received levels of sound. When
Level B Harassment is predicted based
on estimated behavioral responses,
those takes may have a stress-related
physiological component as well.
In the effects section above, we
described the Southall et al., (2007)
severity scaling system and listed some
examples of the three broad categories
of behaviors: (0–3: Minor and/or brief
behaviors); 4–6 (Behaviors with higher
potential to affect foraging,
reproduction, or survival); 7–9
(Behaviors considered likely to affect
the aforementioned vital rates).
Generally speaking, MMPA Level B
Harassment, as defined in this
document, would include the behaviors
described in the 7–9 category, and a
subset, dependent on context and other
considerations, of the behaviors
described in the 4–6 categories.
Behavioral harassment generally does
not include behaviors ranked 0–3 in
Southall et al., (2007).
Acoustic Masking and
Communication Impairment—Acoustic
masking is considered Level B
Harassment, as it can disrupt natural
behavioral patterns by interrupting or
limiting the marine mammal’s receipt or
transmittal of important information or
environmental cues.
TTS—As discussed previously, TTS
can affect how an animal behaves in
response to the environment, including
conspecifics, predators, and prey. The
following physiological mechanisms are
thought to play a role in inducing
auditory fatigue: Effects to sensory hair
cells in the inner ear that reduce their
sensitivity, modification of the chemical
environment within the sensory cells,
residual muscular activity in the middle
ear, displacement of certain inner ear
membranes, increased blood flow, and
post-stimulatory reduction in both
efferent and sensory neural output.
Ward (1997) suggested that when these
effects result in TTS rather than PTS,
they are within the normal bounds of
physiological variability and tolerance
and do not represent a physical injury.
Additionally, Southall et al. (2007)
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indicate that although PTS is a tissue
injury, TTS is not because the reduced
hearing sensitivity following exposure
to intense sound results primarily from
fatigue, not loss, of cochlear hair cells
and supporting structures and is
reversible. Accordingly, NMFS classifies
TTS (when resulting from exposure to
active acoustic sources) as Level B
Harassment, not Level A Harassment
(injury).
Level A Harassment
Of the potential effects that were
described in the Potential Impacts to
Marine Mammal Species section,
following are the types of effects that
fall into the Level A Harassment
category:
PTS—PTS (resulting either from
exposure to active acoustic sources) is
irreversible and considered an injury.
PTS results from exposure to intense
sounds that cause a permanent loss of
inner or outer cochlear hair cells or
exceed the elastic limits of certain
tissues and membranes in the middle
and inner ears and results in changes in
the chemical composition of the inner
ear fluids.
Acoustically Mediated Bubble
Growth—A few theories suggest ways in
which gas bubbles become enlarged
through exposure to intense sounds
(HFAS/MFAS) to the point where tissue
damage results. In rectified diffusion,
exposure to a sound field would cause
bubbles to increase in size. Alternately,
bubbles could be destabilized by high
level sound exposures such that bubble
growth then occurs through static
diffusion of gas out of the tissues. Tissue
damage from either of these processes
would be considered an injury.
Behaviorally Mediated Bubble
Growth—Several authors suggest
mechanisms in which marine mammals
could behaviorally respond to exposure
to HFAS/MFAS by altering their dive
patterns in a manner (unusually rapid
ascent, unusually long series of surface
dives, etc.) that might result in unusual
bubble formation or growth ultimately
resulting in tissue damage (emboli, etc.).
Acoustic Take Criteria for Naval Sonar
For the purposes of an MMPA
incidental take authorization, three
types of take are identified: Level B
harassment; Level A harassment; and
mortality (or serious injury leading to
mortality). The categories of marine
mammal responses (physiological and
behavioral) that fall into the two
harassment categories were described in
the previous section.
Because the physiological and
behavioral responses of the majority of
the marine mammals exposed to HFAS/
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MFAS cannot be detected or measured,
a method is needed to estimate the
number of individuals that will be
taken, pursuant to the MMPA, based on
the proposed action. To this end, NMFS
uses acoustic criteria that estimate the
received level (when exposed to HFAS/
MFAS) at which Level B or Level A
harassment would occur. The acoustic
criteria for HFAS/MFAS are discussed
below.
Because relatively few applicable data
exist to support acoustic criteria
specifically for HFAS, and it is
suspected that the majority of the
adverse effects are from the MFAS due
to their larger impact ranges, NMFS will
apply the criteria developed for the
MFAS to the HFAS as well.
NMFS utilizes three acoustic criteria
for HFAS/MFAS: PTS (injury—Level A
Harassment), behavioral harassment
from TTS, and sub-TTS (Level B
Harassment). Because the TTS and PTS
criteria are derived similarly and the
PTS criteria was extrapolated from the
TTS data, the TTS and PTS acoustic
criteria will be presented first, before
the behavioral criteria. For more
information regarding these criteria,
please see the Navy’s LOA application
for the Keyport Range Complex RDT&E
and range extension activities.
Level B Harassment Threshold (TTS)
As mentioned above, behavioral
disturbance, acoustic masking, and TTS
are all considered Level B Harassment.
Marine mammals would usually be
behaviorally disturbed at lower received
levels than those at which they would
likely sustain TTS, so the levels at
which behavioral disturbance is likely
to occur are considered the onset of
Level B Harassment. The behavioral
responses of marine mammals to sound
are variable, context specific, and,
therefore, difficult to quantify (see Risk
Function section, below). TTS is a
physiological effect that has been
studied and quantified in laboratory
conditions. NMFS also uses an acoustic
criteria to estimate the number of
marine mammals that might sustain
TTS incidental to a specific activity (in
addition to the behavioral criteria).
A number of investigators have
measured TTS in marine mammals.
These studies measured hearing
thresholds in trained marine mammals
before and after exposure to intense
sounds. The existing cetacean TTS data
are summarized in the following bullets.
• Schlundt et al. (2000) reported the
results of TTS experiments conducted
with 5 bottlenose dolphins and 2
belugas exposed to 1-second tones. This
paper also includes a reanalysis of
preliminary TTS data released in a
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technical report by Ridgway et al.
(1997). At frequencies of 3, 10, and 20
kHz, sound pressure levels (SPLs)
necessary to induce measurable
amounts (6 dB or more) of TTS were
between 192 and 201 dB re 1 microPa
(EL = 192 to 201 dB re 1 microPa2-s).
The mean exposure SPL and EL for
onset-TTS were 195 dB re 1 microPa
and 195 dB re 1 microPa2-s,
respectively.
• Finneran et al. (2001, 2003, 2005)
described TTS experiments conducted
with bottlenose dolphins exposed to 3kHz tones with durations of 1, 2, 4, and
8 seconds. Small amounts of TTS (3 to
6 dB) were observed in one dolphin
after exposure to ELs between 190 and
204 dB re 1 microPa2-s. These results
were consistent with the data of
Schlundt et al. (2000) and showed that
the Schlundt et al. (2000) data were not
significantly affected by the masking
sound used. These results also
confirmed that, for tones with different
durations, the amount of TTS is best
correlated with the exposure EL rather
than the exposure SPL.
• Nachtigall et al. (2003) measured
TTS in a bottlenose dolphin exposed to
octave-band sound centered at 7.5 kHz.
Nachtigall et al. (2003a) reported TTSs
of about 11 dB measured 10 to 15
minutes after exposure to 30 to 50
minutes of sound with SPL 179 dB re
1 microPa (EL about 213 dB re
microPa2-s). No TTS was observed after
exposure to the same sound at 165 and
171 dB re 1 microPa. Nachtigall et al.
(2004) reported TTSs of around 4 to 8
dB 5 minutes after exposure to 30 to 50
minutes of sound with SPL 160 dB re
1 microPa (EL about 193 to 195 dB re
1 microPa2-s). The difference in results
was attributed to faster post exposure
threshold measurement—TTS may have
recovered before being detected by
Nachtigall et al. (2003). These studies
showed that, for long duration
exposures, lower sound pressures are
required to induce TTS than are
required for short-duration tones.
• Finneran et al. (2000, 2002)
conducted TTS experiments with
dolphins and belugas exposed to
impulsive sounds similar to those
produced by distant underwater
explosions and seismic waterguns.
These studies showed that, for very
short-duration impulsive sounds, higher
sound pressures were required to
induce TTS than for longer-duration
tones.
• Mooney et al. (2009) exposed a
bottlenose dolphin with a ‘‘typical’’
mid-frequency naval sonar signal (two
down sweeps of 0.5 s each separated by
a 0.5 s gap, fundamental frequency
approximately 3–4 kHz with multiple
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32283
harmonics) recorded within the Puget
Sound, Washington. Successive threeping blocks, each block spaced 24 s
apart, were used to simulate a ‘‘typical’’
mid-frequency sonar application. To
evaluate TTS, hearing thresholds for a
5.6 kHz tone were measured before and
after noise exposure using the
physiological method of auditory
evoked potentials. Sonar SPLs were
gradually increased up to 203 dB SPL
(rms) (measured at the location of the
dolphin’s ear) for individual pings. The
ping number was then increased over
multiple exposure sessions until a
threshold shift was induced. Results
showed that only the five blocks of
sonar pings, presenting an SPL of 203
dB (SEL of 214 dB re 1 microPa2-s),
reliably induced shifts for three
consecutive research sessions.
• Kastak et al. (1999a, 2005)
conducted TTS experiments with three
species of pinnipeds, California sea lion,
northern elephant seal and a Pacific
harbor seal, exposed to continuous
underwater sounds at levels of 80 and
95 dB sensation level (the level above its
hearing threshold) at 2.5 and 3.5 kHz for
up to 50 minutes. Mean TTS shifts of up
to 12.2 dB occurred with the harbor
seals showing the largest shift of 28.1
dB. Increasing the sound duration had
a greater effect on TTS than increasing
the sound level from 80 to 95 dB.
Some of the more important data
obtained from these studies are onsetTTS levels (exposure levels sufficient to
cause a just-measurable amount of TTS)
often defined as 6 dB of TTS (for
example, Schlundt et al., 2000) and the
fact that energy metrics (sound exposure
levels (SEL), which include a duration
component) better predict when an
animal will sustain TTS than pressure
(SPL) alone. NMFS’ TTS criteria (which
indicate the received level at which
onset TTS (<6dB) is induced, expressed
in SELs) for HFAS/MFAS are as follows:
• Cetaceans—195 dB re 1 microPa2-s
(based on mid-frequency cetaceans—no
published data exist on auditory effects
of noise in low or high frequency
cetaceans (Southall et al., 2007)).
• Pinnipeds:
—Harbor Seals (and closely related
species)—183 dB re 1 microPa2-s
—Northern Elephant Seals (and closely
related species)—204 dB re 1
microPa2-s
—California Sea Lions (and closely
related species)—206 dB re 1
microPa2-s
A detailed description of how TTS
criteria were derived from the results of
the above studies may be found in
Chapter 3 of Southall et al. (2007), as
well as the Navy’s Keyport Range
Complex LOA application.
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Level A Harassment Threshold (PTS)
For acoustic effects, because the
tissues of the ear appear to be the most
susceptible to the physiological effects
of sound, and because threshold shifts
tend to occur at lower exposures than
other more serious auditory effects,
NMFS has determined that PTS is the
best indicator for the smallest degree of
injury that can be measured. Therefore,
the acoustic exposure associated with
onset-PTS is used to define the lower
limit of the Level A harassment.
PTS data do not currently exist for
marine mammals and are unlikely to be
obtained due to ethical concerns.
However, PTS levels for these animals
may be estimated using TTS data from
marine mammals and relationships
between TTS and PTS that have been
discovered through study of terrestrial
mammals. NMFS uses the following
acoustic criteria for injury (expressed in
SELs):
• Cetaceans—215 dB re 1 microPa2-s
(based on mid-frequency cetaceans—no
published data exist on auditory effects
of noise in low or high frequency
cetaceans (Southall et al., 2007)).
• Pinnipeds:
—Harbor Seals (and closely related
species)—203 dB re 1 microPa2-s
—Northern Elephant Seals (and closely
related species)—224 dB re 1
microPa2-s
—California Sea Lions (and closely
related species)—226 dB re 1
microPa2-s
These criteria are based on a 20 dB
increase in SEL over that required for
onset-TTS. Extrapolations from
terrestrial mammal data indicate that
PTS occurs at 40 dB or more of TS, and
that TS growth occurs at a rate of
approximately 1.6 dB TS per dB
increase in EL. There is a 34-dB TS
difference between onset-TTS (6 dB)
and onset-PTS (40 dB). Therefore, an
animal would require approximately 20dB of additional exposure (34 dB
divided by 1.6 dB) above onset-TTS to
reach PTS. A detailed description of
how TTS criteria were derived from the
results of the above studies may be
found in Chapter 3 of Southall et al.
(2007), as well as the Navy’s Keyport
Range Complex LOA application.
Southall et al. (2007) recommend a
precautionary dual criteria for TTS (230
dB re 1 microPa (SPL) in addition to 215
re 1 microPa2-s (SEL)) to account for the
potentially damaging transients
embedded within non-pulse exposures.
However, in the case of HFAS/MFAS,
the distance at which an animal would
receive 215 (SEL) is farther from the
source than the distance at which they
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would receive 230 (SPL) and therefore,
it is not necessary to consider 230 dB.
We note here that behaviorally
mediated injuries (such as those that
have been hypothesized as the cause of
some beaked whale strandings) could
potentially occur in response to
received levels lower than those
believed to directly result in tissue
damage. As mentioned previously, data
to support a quantitative estimate of
these potential effects (for which the
exact mechanism is not known and in
which factors other than received level
may play a significant role) do not exist.
Level B Harassment Risk Function
(Behavioral Harassment)
The first MMPA authorization for take
of marine mammals incidental to
tactical active sonar was issued in 2006
for Navy Rim of the Pacific training
exercises in Hawaii. For that
authorization, NMFS used 173 dB SEL
as the criterion for the onset of
behavioral harassment (Level B
Harassment). This type of single number
criterion is referred to as a step function,
in which (in this example) all animals
estimated to be exposed to received
levels above 173 dB SEL would be
predicted to be taken by Level B
Harassment and all animals exposed to
less than 173 dB SEL would not be
taken by Level B Harassment. As
mentioned previously, marine mammal
behavioral responses to sound are
highly variable and context specific
(affected by differences in acoustic
conditions; differences between species
and populations; differences in gender,
age, reproductive status, or social
behavior; or the prior experience of the
individuals), which does not support
the use of a step function to estimate
behavioral harassment.
Unlike step functions, acoustic risk
continuum functions (which are also
called ‘‘exposure-response functions,’’
‘‘dose-response functions,’’ or ‘‘stress
response functions’’ in other risk
assessment contexts) allow for
probability of a response that NMFS
would classify as harassment to occur
over a range of possible received levels
(instead of one number) and assume that
the probability of a response depends
first on the ‘‘dose’’ (in this case, the
received level of sound) and that the
probability of a response increases as
the ‘‘dose’’ increases. The Navy and
NMFS have previously used acoustic
risk functions to estimate the probable
responses of marine mammals to
acoustic exposures in the Navy FEISs on
SURTASS LFA sonar (DoN, 2001c) and
the North Pacific Acoustic Laboratory
experiments conducted off the Island of
Kauai (ONR, 2001). The specific risk
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functions used here were also used in
the MMPA regulations and FEIS for
Hawaii Range Complex (HRC), Southern
California Range Complex (SOCAL),
Atlantic Fleet Active Sonar Testing
(AFAST), and the Naval Surface Warfare
Center Panama City Division (NSWC
PCD) mission activities. As discussed in
the Effects section, factors other than
received level (such as distance from or
bearing to the sound source) can affect
the way that marine mammals respond;
however, data to support a quantitative
analysis of those (and other factors) do
not currently exist. NMFS will continue
to modify these criteria as new data
become available.
The methodology described below is
based on surface ship acoustic sources.
The NAVSEA NUWC Keyport Range
does not utilize these sources in RDT&E
activities. It should be noted though,
that the sources methodology described
below is utilized for the modeling of
potential exposures to mid- and highfrequency active sonar.
To assess the potential effects on
marine mammals associated with active
sonar used during training activity the
Navy and NMFS applied a risk function
that estimates the probability of
behavioral responses that NMFS would
classify as harassment for the purposes
of the MMPA given exposure to specific
received levels of MFA sonar. The
mathematical function is derived from a
solution in Feller (1968) as defined in
the SURTASS LFA Sonar Final OEIS/
EIS (DoN, 2001), and relied on in the
Supplemental SURTASS LFA Sonar EIS
(DoN, 2007a), for the probability of MFA
sonar risk for Level B behavioral
harassment with input parameters
modified by NMFS for MFA sonar for
mysticetes and odontocetes (NMFS,
2008). The same risk function and input
parameters will be applied to high
frequency active (HFA) (<10 kHz)
sources until applicable data become
available for high frequency sources.
In order to represent a probability of
risk, the function should have a value
near zero at very low exposures, and a
value near one for very high exposures.
One class of functions that satisfies this
criterion is cumulative probability
distributions, a type of cumulative
distribution function. In selecting a
particular functional expression for risk,
several criteria were identified:
• The function must use parameters
to focus discussion on areas of
uncertainty;
• The function should contain a
limited number of parameters;
• The function should be capable of
accurately fitting experimental data; and
• The function should be reasonably
convenient for algebraic manipulations.
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As described in U.S. Department of
the Navy (2001), the mathematical
function below is adapted from a
solution in Feller (1968).
−A
⎛ L−B⎞
1− ⎜
⎟
⎝ K ⎠
R=
−2A
⎛ L−B⎞
1− ⎜
⎟
⎝ K ⎠
Where:
R = Risk (0–1.0)
L = Received level (dB re: 1 μPa)
B = Basement received level = 120 dB re: 1
μPa
K = Received level increment above B where
50 percent risk = 45 dB re: 1 μPa
A = Risk transition sharpness parameter = 10
(odontocetes) or 8 (mysticetes)
In order to use this function to
estimate the percentage of an exposed
population that would respond in a
manner that NMFS classifies as Level B
harassment, based on a given received
level, the values for B, K and A need to
be identified.
B Parameter (Basement)—The B
parameter is the estimated received
level below which the probability of
disruption of natural behavioral
patterns, such as migration, surfacing,
nursing, breeding, feeding, or sheltering,
to a point where such behavioral
patterns are abandoned or significantly
altered approaches zero for the HFAS/
MFAS risk assessment. At this received
level, the curve would predict that the
percentage of the exposed population
that would be taken by Level B
Harassment approaches zero. For HFAS/
MFAS, NMFS has determined that B =
120 dB re 1 μPa (SPL). This level is
based on a broad overview of the levels
at which many species have been
reported responding to a variety of
sound sources.
K Parameter (Representing the 50Percent Risk Point)—The K parameter is
based on the received level that
corresponds to 50 percent risk, or the
received level at which we believe 50
percent of the animals exposed to the
designated received level will respond
in a manner that NMFS classifies as
Level B Harassment. The K parameter (K
= 45 dB) is based on three datasets in
which marine mammals exposed to
mid-frequency sound sources were
reported to respond in a manner that
NMFS would classify as Level B
Harassment. There is widespread
consensus that marine mammal
responses to HFA/MFA sound signals
need to be better defined using
controlled exposure experiments (Cox et
al., 2006; Southall et al., 2007). The
Navy is contributing to an ongoing
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behavioral response study in the
Bahamas that is expected to provide
some initial information on beaked
whales, the species identified as the
most sensitive to MFAS. NMFS is
leading this international effort with
scientists from various academic
institutions and research organizations
to conduct studies on how marine
mammals respond to underwater sound
exposures. Until additional data are
available, however, NMFS and the Navy
have determined that the following
three data sets are most applicable for
direct use in establishing the K
parameter for the HFAS/MFAS risk
function. These data sets, summarized
below, represent the only known data
that specifically relate altered
behavioral responses (that NMFS would
consider Level B Harassment) to
exposure to HFAS/MFAS sources.
Even though these data are considered
the most representative of the proposed
specified activities, and therefore the
most appropriate on which to base the
K parameter (which basically
determines the midpoint) of the risk
function, these data have limitations,
which are discussed in Appendix C of
the NAVSEA NUWC Keyport Range
Complex Extension EIS/OEIS.
1. Controlled Laboratory Experiments
with Odontocetes (SSC Dataset)—Most
of the observations of the behavioral
responses of toothed whales resulted
from a series of controlled experiments
on bottlenose dolphins and beluga
whales conducted by researchers at
SSC’s facility in San Diego, California
(Finneran et al., 2001, 2003, 2005;
Finneran and Schlundt, 2004; Schlundt
et al., 2000). In experimental trials
(designed to measure TTS) with marine
mammals trained to perform tasks when
prompted, scientists evaluated whether
the marine mammals performed these
tasks when exposed to mid-frequency
tones. Altered behavior during
experimental trials usually involved
refusal of animals to return to the site
of the sound stimulus, but also included
attempts to avoid an exposure in
progress, aggressive behavior, or refusal
to further participate in tests.
Finneran and Schlundt (2004)
examined behavioral observations
recorded by the trainers or test
coordinators during the Schlundt et al.
(2000) and Finneran et al. (2001, 2003,
2005) experiments. These included
observations from 193 exposure sessions
(fatiguing stimulus level > 141 dB re
1microPa) conducted by Schlundt et al.
(2000) and 21 exposure sessions
conducted by Finneran et al. (2001,
2003, 2005). The TTS experiments that
supported Finneran and Schlundt
(2004) are further explained below:
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• Schlundt et al. (2000) provided a
detailed summary of the behavioral
responses of trained marine mammals
during TTS tests conducted at SSC San
Diego with 1-sec tones and exposure
frequencies of 0.4 kHz, 3 kHz, 10 kHz,
20 kHz and 75 kHz. Schlundt et al.
(2000) reported eight individual TTS
experiments. The experiments were
conducted in San Diego Bay. Because of
the variable ambient noise in the bay,
low-level broadband masking noise was
used to keep hearing thresholds
consistent despite fluctuations in the
ambient noise. Schlundt et al. (2000)
reported that ‘‘behavioral alterations,’’
or deviations from the behaviors the
animals being tested had been trained to
exhibit, occurred as the animals were
exposed to increasing fatiguing stimulus
levels.
• Finneran et al. (2001, 2003, 2005)
conducted two separate TTS
experiments using 1-sec tones at 3 kHz.
The test methods were similar to that of
Schlundt et al. (2000) except the tests
were conducted in a pool with very low
ambient noise level (below 50 dB re 1
microPa2/Hz), and no masking noise
was used. In the first, fatiguing sound
levels were increased from 160 to 201
dB SPL. In the second experiment,
fatiguing sound levels between 180 and
200 dB SPL were randomly presented.
Bottlenose dolphins exposed to 1-sec
intense tones exhibited short-term
changes in behavior above received
sound levels of 178 to 193 dB re 1
microPa (rms), and beluga whales did so
at received levels of 180 to 196 dB and
above.
2. Mysticete Field Study (Nowacek et
al., 2004)—The only available and
applicable data relating mysticete
responses to exposure to mid-frequency
sound sources are from Nowacek et al.
(2004). Nowacek et al. (2004)
documented observations of the
behavioral response of North Atlantic
right whales exposed to alert stimuli
containing mid-frequency components
in the Bay of Fundy. Investigators used
archival digital acoustic recording tags
(DTAG) to record the behavior (by
measuring pitch, roll, heading, and
depth) of right whales in the presence
of an alert signal, and to calibrate
received sound levels. The alert signal
was 18 minutes of exposure consisting
of three 2-minute signals played
sequentially three times over. The three
signals had a 60 percent duty cycle and
consisted of: (1) Alternating 1-sec pure
tones at 500 Hz and 850 Hz; (2) a 2-sec
logarithmic down-sweep from 4,500 Hz
to 500 Hz; and (3) a pair of low (1,500
Hz)-high (2,000 Hz) sine wave tones
amplitude modulated at 120 Hz and
each 1 sec long. The purposes of the
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alert signal were (a) to pique the
mammalian auditory system with
disharmonic signals that cover the
whales’ estimated hearing range; (b) to
maximize the signal to noise ratio
(obtain the largest difference between
background noise) and (c) to provide
localization cues for the whale. The
maximum source level used was 173 dB
SPL.
Nowacek et al. (2004) reported that
five out of six whales exposed to the
alert signal with maximum received
levels ranging from 133 to 148 dB re 1
microPa significantly altered their
regular behavior and did so in identical
fashion. Each of these five whales: (i)
Abandoned their current foraging dive
prematurely as evidenced by curtailing
their ‘bottom time’; (ii) executed a
shallow-angled, high power (i.e.,
significantly increased fluke stroke rate)
ascent; (iii) remained at or near the
surface for the duration of the exposure,
an abnormally long surface interval; and
(iv) spent significantly more time at
subsurface depths (1–10 m) compared
with normal surfacing periods, when
whales normally stay within 1 m (1.1
yd) of the surface.
3. Odontocete Field Data (Haro
Strait—USS SHOUP)—In May 2003,
killer whales were observed exhibiting
behavioral responses generally
described as avoidance behavior while
the U.S. Ship (USS) SHOUP was
engaged in MFAS in the Haro Strait in
the vicinity of Puget Sound,
Washington. Those observations have
been documented in three reports
developed by Navy and NMFS (NMFS,
2005a; Fromm, 2004a, 2004b; DON,
2003). Although these observations were
made in an uncontrolled environment,
the sound field that may have been
associated with the sonar operations
was estimated using standard acoustic
propagation models that were verified
(for some but not all signals) based on
calibrated in situ measurements from an
independent researcher who recorded
the sounds during the event. Behavioral
observations were reported for the group
of whales during the event by an
experienced marine mammal biologist
who happened to be on the water
studying them at the time. The
observations associated with the USS
SHOUP provide the only data set
available of the behavioral responses of
wild, non-captive animals upon actual
exposure to AN/SQS–53 sonar.
U.S. Department of Commerce
(NMFS, 2005a); U.S. Department of the
Navy (2004b); Fromm (2004a, 2004b)
documented reconstruction of sound
fields produced by USS SHOUP
associated with the behavioral response
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of killer whales observed in Haro Strait.
Observations from this reconstruction
included an approximate closest
approach time which was correlated to
a reconstructed estimate of received
level (which ranged from 150 to 180 dB)
at an approximate whale location with
a mean value of 169.3 dB SPL.
Calculation of K Parameter—NMFS
and the Navy used the mean of the
following values to define the midpoint
of the function: (1) The mean of the
lowest received levels (185.3 dB) at
which individuals responded with
altered behavior to 3 kHz tones in the
SSC data set; (2) the estimated mean
received level value of 169.3 dB
produced by the reconstruction of the
USS SHOUP incident in which killer
whales exposed to MFA sonar (range
modeled possible received levels: 150 to
180 dB); and (3) the mean of the 5
maximum received levels at which
Nowacek et al. (2004) observed
significantly altered responses of right
whales to the alert stimuli than to the
control (no input signal) is 139.2 dB
SPL. The arithmetic mean of these three
mean values is 165 dB SPL. The value
of K is the difference between the value
of B (120 dB SPL) and the 50 percent
value of 165 dB SPL; therefore, K=45.
A Parameter (Steepness)—NMFS
determined that a steepness parameter
(A)=10 is appropriate for odontocetes
(except harbor porpoises) and pinnipeds
and A=8 is appropriate for mysticetes.
The use of a steepness parameter of
A=10 for odontocetes (except harbor
porpoises) for the HFAS/MFAS risk
function was based on the use of the
same value for the SURTASS LFA risk
continuum, which was supported by a
sensitivity analysis of the parameter
presented in Appendix D of the
SURTASS/LFA FEIS (DoN, 2001c). As
concluded in the SURTASS FEIS/EIS,
the value of A=10 produces a curve that
has a more gradual transition than the
curves developed by the analyses of
migratory gray whale studies (Malme et
al., 1984; Buck and Tyack, 2000; and
SURTASS LFA Sonar EIS, Subchapters
1.43, 4.2.4.3 and Appendix D, and
NMFS, 2008).
NMFS determined that a lower
steepness parameter (A=8), resulting in
a shallower curve, was appropriate for
use with mysticetes and HFAS/MFAS.
The Nowacek et al. (2004) dataset
contains the only data illustrating
mysticete behavioral responses to a midfrequency sound source. A shallower
curve (achieved by using A=8) better
reflects the risk of behavioral response
at the relatively low received levels at
which behavioral responses of right
whales were reported in the Nowacek et
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al. (2004) data. Compared to the
odontocete curve, this adjustment
results in an increase in the proportion
of the exposed population of mysticetes
being classified as behaviorally harassed
at lower RLs, such as those reported
here and is supported by the only
dataset currently available.
Basic Application of the Risk
Function—The risk function is used to
estimate the percentage of an exposed
population that is likely to exhibit
behaviors that would qualify as
harassment (as that term is defined by
the MMPA applicable to military
readiness activities, such as the Navy’s
testing and research activities with
HFA/MFA sonar) at a given received
level of sound. For example, at 165 dB
SPL (dB re 1 Pa rms), the risk (or
probability) of harassment is defined
according to this function as 50 percent,
and Navy/NMFS applies that by
estimating that 50 percent of the
individuals exposed at that received
level are likely to respond by exhibiting
behavior that NMFS would classify as
behavioral harassment. The risk
function is not applied to individual
animals, only to exposed populations.
The data primarily used to produce
the risk function (the K parameter) were
compiled from four species that had
been exposed to sound sources in a
variety of different circumstances. As a
result, the risk function represents a
general relationship between acoustic
exposures and behavioral responses that
is then applied to specific
circumstances. That is, the risk function
represents a relationship that is deemed
to be generally true, based on the
limited, best-available science, but may
not be true in specific circumstances. In
particular, the risk function, as currently
derived, treats the received level as the
only variable that is relevant to a marine
mammal’s behavioral response.
However, we know that many other
variables—the marine mammal’s
gender, age, and prior experience, the
activity it is engaged in during an
exposure event, its distance from a
sound source, the number of sound
sources, and whether the sound sources
are approaching or moving away from
the animal—can be critically important
in determining whether and how a
marine mammal will respond to a sound
source (Southall et al., 2007). The data
that are currently available do not allow
for incorporation of these other
variables in the current risk functions;
however, the risk function represents
the best use of the data that are available
(Figure 1).
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As more specific and applicable data
become available for HFAS/MFAS
sources, NMFS can use these data to
modify the outputs generated by the risk
function to make them more realistic.
Ultimately, data may exist to justify the
use of additional, alternate, or
multivariate functions. For example, as
mentioned previously, the distance from
the sound source and whether it is
perceived as approaching or moving
away can affect the way an animal
responds to a sound (Wartzok et al.,
2003).
Specific Consideration for Harbor
Porpoises
The information currently available
regarding these inshore species that
inhabit shallow and coastal waters
suggests a very low threshold level of
response for both captive and wild
animals. Threshold levels at which both
captive (e.g., Kastelein et al., 2000;
2005a; 2006) and wild harbor porpoises
(e.g., Johnston, 2002) responded to
sound (e.g., acoustic harassment devices
(ADHs), acoustic deterrent devices
(ADDs), or other non-pulsed sound
sources) is very low (e.g., ∼120 dB SPL),
although the biological significance of
the disturbance is uncertain. Therefore,
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the risk function curve as presented is
not used. Instead, a step function
threshold of 120 dB SPL is used to
estimate take of harbor porpoises (i.e.,
assumes that all harbor porpoises
exposed to 120 dB or higher MFAS/
HFAS will respond in a way NMFS
considers behavioral harassment).
Modeling Acoustic Effects
The methodology for analyzing
potential impacts from mid- and highfrequency acoustic sources is presented
in this section, which defines the model
process in detail, describes how the
impact threshold derived from NavyNMFS consultations are derived, and
discusses relative potential impact
based on species biology.
Modeling methods applied herein
were originally developed for midfrequency (1–10 kHz) active (MFA)
sonars (e.g., surface-ship hull-mounted
sonars, which are not used in the
NAVSEA NUWC Keyport Range
Complex). Nevertheless, the methods
and thresholds are agreed upon by the
U.S. Navy and NMFS as the best
available science with which to
determine the extent of physiological or
behavioral effects on marine mammals
that would result from the use of mid-
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frequency active (MFA) and high
frequency active (HFA) acoustic sources
for this proposed action. Detailed
descriptions of the modeling process
and results are provided in LOA
Application.
The Navy acoustic exposure model
process uses a number of inter-related
software tools to assess potential
exposure of marine mammals to Navy
generated underwater sound. For sonar,
these tools estimate potential impact
volumes and areas over a range of
thresholds for sonar specific operating
modes. Results are based upon
extensive pre-computations over the
range of acoustic environments that
might be encountered in the operating
area.
The process includes four steps used
to calculate potential exposures:
• Identify unique acoustic
environments that encompass the
operating area. Parameters include
depth and seafloor geography, bottom
characteristics and sediment type, wind
and surface roughness, sound velocity
profile, surface duct, sound channel,
and convergence zones.
• Compute transmission loss (TL)
data appropriate for each sensor type in
each of these acoustic environments.
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Propagation can be complex depending
on a number of environmental
parameters listed in step one, as well as
sonar operating parameters such as
directivity, source level, ping rate, and
ping length. The Navy standard CASS–
GRAB acoustic propagation model is
used to resolve these complexities for
underwater propagation prediction.
• Use that TL to estimate the total
sound energy received at each point in
the acoustic environment.
• Apply this energy to predicted
animal density for that area to estimate
potential acoustic exposure, with
animals distributed in 3–D based on
best available science on animal dive
profiles.
The primary potential impact to
marine mammals from underwater
acoustics is Level B harassment from
noise. A certain proportion of marine
mammals are expected to experience
behavioral disturbance at different
received sound pressure levels and are
counted as Level B harassment
exposures. A detailed discussion of the
modeling is provided in the Navy’s LOA
application.
Step 1. Acoustic Sources
For modeling purposes, acoustic
source parameters were based on
records from previous RDT&E activities,
to reflect the underwater sound use
expected to occur during activities in
the NAVSEA NUWC Keyport Range
Complex. The actual acoustic source
parameters in many cases are classified,
however, modeling used to calculate
exposures to marine mammals
employed actual and preferred
parameters which have in the past been
used during RDT&E activities in the
NAVSEA NUWC Keyport Range
Complex.
Every use of underwater acoustic
energy includes the potential to harass
marine animals in the vicinity of the
source. The number of animals exposed
to potential harassment in any such
action is dictated by the propagation
field and the manner in which the
acoustic source is operated (i.e., source
level, depth, frequency, pulse length,
directivity, platform speed, repetition
rate). A wide variety of systems/
equipment that utilize narrowband
acoustic sources are employed at the
NAVSEA NUWC Keyport Range
Complex. Eight have been selected as
representative of the types of operating
in this range and are described in Table
8. Take estimates for these sources are
calculated and reported on a per-run
basis.
TABLE 8—MID- AND HIGH-FREQUENCY ACOUSTIC SOURCES EMPLOYED IN THE KEYPORT RANGE COMPLEX
S1
S2
S3
S4
S5
S6
S7
S8
........................................
........................................
........................................
........................................
........................................
........................................
........................................
........................................
Acoustic source description
Frequency class
Sub-bottom profiler .................................
UUV source .............................................
REMUS Modem ......................................
REMUS–SAS–HF ...................................
Range Target ..........................................
Test Vehicle 1 .........................................
Test Vehicle 2 .........................................
Test Vehicle 3 .........................................
Mid-frequency .........................................
High-frequency ........................................
Mid-frequency .........................................
High-frequency ........................................
Mid-frequency .........................................
High-frequency ........................................
High-frequency ........................................
High-frequency ........................................
The acoustic modeling that is
necessary to support the take estimates
for each of these sources relies upon a
generalized description of the manner of
the operating modes. This description
includes the following:
• ‘‘Effective’’ energy source level—
The total energy across the band of the
source, scaled by the pulse length (10
log10 [pulse length]).
• Source depth—Depth of the source
in meters. Each source was modeled in
the middle of the water column.
• Nominal frequency—Typically the
center band of the source emission.
These are frequencies that have been
reported in open literature and are used
to avoid classification issues.
Differences between these nominal
values and actual source frequencies are
small enough to be of little consequence
to the output impact volumes.
• Source directivity—The source
beam is modeled as the product of a
horizontal beam pattern and a vertical
beam pattern. Two parameters define
the horizontal beam pattern:
• Horizontal beam width—Width of
the source beam (degrees) in the
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horizontal plane (assumed constant for
all horizontal steer directions).
• Horizontal steer direction—
Direction in the horizontal in which the
beam is steered relative to the direction
in which the platform is heading.
The horizontal beam has constant
response across the width of the beam
and with flat, 20-dB down sidelobes.
(Note that steer directions j, ¥j, 180o
¥ j, and 180o + j all produce equal
impact volumes.)
Similarly, two parameters define the
vertical beam pattern:
• Vertical beam width—Width of the
source beam (degrees) in the vertical
plane measured at the 3-dB down point.
(The width is that of the beam steered
towards broadside and not the width of
the beam at the specified vertical steer
direction.)
• Vertical steer direction—Direction
in the vertical plane that the beam is
steered relative to the horizontal
(upward looking angles are positive).
To avoid sharp transitions that a
rectangular beam might introduce, the
power response at vertical angle q is
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Takes reported
Per
Per
Per
Per
Per
Per
Per
Per
4-hour run.
2-hour run.
2-hour run.
2-hour run.
20-minute run.
10-minute run.
10-minute run.
10-minute run.
⎧ sin 2 ⎢ n (θ − θ ) ⎥
⎫
⎪
s
⎣
⎦ , 0.01⎪
max ⎨
⎬
2
⎪ ⎡ n sin (θ s − θ ) ⎤
⎪
⎦
⎩⎣
⎭
where n = 180°/qw is the number of halfwavelength-spaced elements in a line
array that produces a main lobe with a
beam width of qw. qs is the vertical beam
steer direction.
Ping spacing—Distance between
pings. For most sources this is generally
just the product of the speed of advance
of the platform and the repetition rate of
the source. Animal motion is generally
of no consequence as long as the source
motion is greater than the speed of the
animal (nominally, three knots). For
stationary (or nearly stationary) sources,
the ‘‘average’’ speed of the animal is
used in place of the platform speed. The
attendant assumption is that the animals
are all moving in the same constant
direction.
These parameters are defined for each
of the acoustic sources in the following
Table 9.
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TABLE 9—DESCRIPTION OF NAVSEA NUWC KEYPORT RANGE COMPLEX SOURCES
Acoustic source description
Center frequency
Sub-bottom profiler .............................
UUV source .........................................
REMUS Modem ..................................
REMUS–SAS–HF ...............................
Range Target ......................................
Test Vehicle 1 .....................................
Test Vehicle 2 .....................................
Test Vehicle 3 .....................................
4.5 kHz .................
15 kHz ..................
10 kHz ..................
150 kHz ................
5 kHz ....................
20 kHz ..................
25 kHz ..................
30 kHz ..................
Step 2. Environmental Provinces
Propagation loss ultimately
determines the extent of the Zone of
Influence (ZOI) for a particular source
activity. Propagation loss as a function
of range responds to a number of
environmental parameters:
• Water depth
• Sound speed variability throughout
the water column
• Bottom geo-acoustic properties, and
• Wind speed
Due to the importance that
propagation loss plays in modeling
effects, the Navy has over the last four
to five decades invested heavily in
measuring and modeling these
environmental parameters. The result of
this effort is the following collection of
global databases of these environmental
parameters, most of which are accepted
as standards for all Navy modeling
efforts.
• Water depth—Digital Bathymetry
Data Base Variable Resolution (DBDBV)
• Sound speed—Generalized Digital
Environmental Model (GDEM)
• Bottom loss—Low-Frequency
Bottom Loss (LFBL), Sediment
Thickness Database, and HighFrequency Bottom Loss (HFBL), and
• Wind speed—U.S. Navy Marine
Climatic Atlas of the World
Representative environmental
parameters are selected for each of the
three operating areas: DBRC, Keyport,
and Quinault. Sources of local
environmental-acoustic properties were
supplemented with Navy Standard
OAML data to determine model inputs
for bathymetry, sound-speed, and
sediment properties.
The DBRC and Keyport ranges are
located inland with limited water-depth
variability: The maximum water depth
in Dabob Bay is approximately 200
meters; the maximum in the Keyport
range is approximately 30 meters (98
feet). The Quinault range, on the other
hand, is located seaward of the
Washington State Coast to depths
greater than a kilometer.
Sound speed profiles for winter and
summer from the OAML open-ocean
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Source level
207
205
186
220
233
233
230
233
dB
dB
dB
dB
dB
dB
dB
dB
.................
.................
.................
.................
.................
.................
.................
.................
Emission spacing
Vertical directivity
horizontal
0.2 m ....................
1.9 m ....................
45 m .....................
1.9 m ....................
93 m .....................
45 m .....................
540 m ...................
617 m ...................
20 deg ..................
30 deg ..................
60 deg ..................
9 deg ....................
60 deg ..................
20 deg ..................
20 deg ..................
20 deg ..................
database are presented in Figure 6–10 of
the Navy’s LOA application. The winter
profile is a classic half-channel (sound
speed monotonically increasing with
depth). The summer profile consists of
a shallow surface duct over a modest
thermocline. Individual profiles taken
from World Ocean Data Base (NODC,
2005) for DBRC and Keyport are
generally consistent with these openocean profiles. Some of these profiles
exhibit some effects of additional fresh
water near the surface; others have a
little warmer surface layer than this
summer profile. However, the truncated
deep-water profiles are adequately
representative of the inland ranges.
The bottom type in the Quinault range
varies consistently with water depth.
The shallower depths (less than 500
meters) tend to have sandy bottoms
(HFBL class = 2); the deeper depths tend
to be silt (HFBL class = 8).
The sediment type of the DBRC and
Keyport areas that we used for our
modeling were different from those
found in the Low Frequency Bottom
Loss (LFBL) database or implied by the
High-Frequency Bottom Loss (HFBL)
database. Although the water depth of
these areas can be greater that 50 m, the
LFBL database assigned them the
default ‘‘coarse sand’’ sediment type
that was assigned to areas with water
depth less than 50 m (Vidmar, 1994).
Core data from these areas were
collected as part of environmental
monitoring (Llanso, 1998). Cores 14 and
15 from the northern parts of the DBRC
area indicated sediments with sands
and silty sands. A silty sand sediment
type was assigned to these areas (HFBL
class = 2). Core 304R from the southern
part of the DBRC area indicated
sediments with clay. A clay-silt
sediment type (HFBL class = 4) was
assigned to this area taking into account
the transition from the more sandy
northern area to the clay of the southern
area. These assignments are consistent
with the observation (Helton, 1976) that
the boundary area between the northern
and southern areas had sediments that
were mostly mud with a small amount
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Horizontal directivity horizontal
20 deg.
50 deg.
360 deg.
15 deg.
360 deg.
60 deg.
60 deg.
60 deg.
of sand. The Keyport area did not have
any cores in the study area but had three
cores surrounding the area: Core 308R to
the northwest indicated sand sediment;
core 69 to the northeast indicated sand
and silty sand sediments; and core 34 to
the south indicated clay sediment.
Given the surrounding cores we
assigned a sand-silt-clay sediment type
to this area (HFBL class = 4).
The Keyport range has a proposed
extension to the east and south of the
existing boundaries. In addition to the
existing DBRC boundary, there is one
extension to the south and another
extension to the south and the north.
The Quinault range is extended into a
much larger deep-water region
coincident with W–237A with a surf
zone at Pacific Beach.
Step 3. Impact Volumes and Impact
Ranges
Many naval actions include the
potential to injure or harass marine
animals in the neighboring waters
through noise emissions. Given fixed
harassment metrics and thresholds, the
number of animals exposed to potential
harassment in any such action is
dictated by the propagation field and
the characteristics of the noise source.
The expected impact volume
associated with a particular activity is
defined as the expected volume of water
in which some acoustic metric exceeds
a specified threshold. The product of
this volume with a volumetric animal
density yields the expected value of the
number of animals exposed to that
acoustic metric at a level that exceeds
the threshold. There are two acoustic
metrics for mid- and high-frequency
acoustic sources effects: An energy term
(energy flux density) or a pressure term
(peak pressure). The thresholds
associated with each of these metrics
define the levels at which the animals
exposed will experience some degree of
harassment (ranging from behavioral
change to hearing loss).
Impact volume is particularly relevant
when trying to estimate the effect of
repeated source emissions separated in
either time or space. Impact range is
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defined as the maximum range at which
a particular threshold is exceeded for a
single source emission.
The two measures of potential harm
to marine wildlife due to mid- and highfrequency acoustic sources operations
are the accumulated (summed over all
source emissions) energy flux density
received by the animal over the duration
of the activity, and the peak pressure
(loudest sound received) by the animal
over the duration of the activity.
Regardless of the type of source,
estimating the number of animals that
may be harassed in a particular
environment entails the following steps.
• Each source emission is modeled
according to the particular operating
mode of that source. The ‘‘effective’’
energy source level is computed by
integrating over the bandwidth of the
source, and scaling by the pulse length.
The location of the source at the time of
each emission must also be specified.
• For the relevant environmental
acoustic parameters, Transmission Loss
(TL) estimates are computed, sampling
the water column over the appropriate
depth and range intervals. TL data are
sampled at the typical depth(s) of the
source and at the nominal center
frequency of the source.
• The accumulated energy and
maximum sound pressure level (SPL)
are sampled over a volumetric grid
within the waters surrounding a source
action. At each grid point, the received
signal from each source emission is
modeled as the source level reduced by
the appropriate propagation loss from
the location of the source at the time of
each emission to that grid point. The
maximum SPL field is calculated by
taking the maximum level of the
received signal over all emissions, and
the energy field is calculated by
summing the energy of the signal over
all emissions, and adjusting for pulse
length.
• The impact volume for a given
threshold is estimated by summing the
incremental volumes represented by
each grid point for which the
appropriate metric exceeds that
threshold. For maximum SPL,
calculation of the expected volume
represented by each grid point depends
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on the maximum SPL at that point, and
requires an extra step to apply the risk
function.
Finally, the number of takes is
estimated as the product (scalar or
vector, depending upon whether an
animal density depth distribution is
available) of the impact volume and the
animal densities.
(4) Computing Impact Volumes for
Active Sonars
The computation for impact volumes
of active acoustic sources uses the
following steps:
• Identification of the underwater
propagation model used to compute
transmission loss data, a listing of the
source-related inputs to that model, and
a description of the output parameters
that are passed to the energy
accumulation algorithm.
• Definitions of the parameters
describing each acoustic source type.
• Description of the algorithms and
sampling rates associated with the
energy accumulation algorithm.
A detailed discussion of computing
methodologies is provided in the Navy’s
LOA application.
Estimated Takes of Marine Mammals
When analyzing the results of the
acoustic exposure modeling to provide
an estimate of effects, it is important to
understand that there are limitations to
the ecological data used in the model,
and that the model results must be
interpreted within the context of a given
species’ ecology. When reviewing the
acoustic effects modeling results, it is
also important to understand there have
been no confirmed acoustic effects on
any marine species in previous
NAVSEA NUWC Keyport Range
Complex exercises or from any other
mid- and high-frequency active sonar
RDT&E activities within the NAVSEA
NUWC Keyport Range Complex.
The annual estimated number of
exposures from acoustic sources are
given for each species. The modeled
exposure is the probability of a response
that NMFS would classify as harassment
under the MMPA. These exposures are
calculated for all activities modeled and
represent the total exposures per year
and are not based on a per day basis.
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Range Operating Policies and
Procedures (ROP) Description operating
policies and procedures, as described in
NUWC Keyport Report 1509, Range
Operating Policies and Procedures
Manual (ROP), are followed for all
NUWC Keyport range activities. NUWC
Keyport would continue to implement
the ROP policies and procedures within
the NAVSEA NUWC Keyport Range
Complex with implementation of the
proposed range extension. The ROP is
followed to protect the health and safety
of the public and Navy personnel and
equipment as well as to protect the
marine environment. The policies and
procedures address issues such as
safety, development of approved run
plans, range operation personnel
responsibility, deficiency reporting, all
facets of range activities, and the
establishment of ‘‘exclusion zones’’ to
ensure that there are no marine
mammals within a prescribed area prior
to the commencement of each in-water
exercise within the NAVSEA NUWC
Keyport Range Complex. All range
operators are trained by NOAA in
marine mammal identification, and
active acoustic activities are suspended
or delayed if whales, dolphins, or
porpoises (cetaceans) are observed
within range areas.
The modeling for acoustic sources
using the risk function methodology
predicts 15,130 annual acoustic
exposures that result in Level B
harassment and 2,026 annual exposures
of pinnipeds that exceed the TTS
threshold for Level B Harassment under
these criteria. The model predicts 0
annual exposures that exceed the PTS
threshold (Level A Harassment). The
Navy is not requesting Level A
harassment authorization for any marine
mammal. The summary of modeled
mid- and high-frequency acoustic
source exposure harassment numbers by
species are presented in Tables 9
through 12 and represent potential
harassment after implementation of the
ROP. Implementation of the ROP would
result in a zero take with respect to all
cetaceans except for the harbor
porpoise.
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It is highly unlikely that a marine
mammal would experience any longterm effects because the large NAVSEA
NUWC Keyport Range Complex test
areas make individual mammals’
repeated and/or prolonged exposures to
high-level sonar signals unlikely.
Specifically, mid- and high-frequency
acoustic sources have limited marine
mammal exposure ranges and relatively
high platform speeds. Moreover, there
are no exposures that exceed the PTS
threshold and result in Level A
harassment from sonar and other active
acoustic sources. Therefore, long-term
effects on individuals, populations or
stocks are unlikely.
When analyzing the results of the
acoustic exposure modeling to provide
an estimate of effects, it is important to
understand that there are limitations to
the ecological data (diving behavior,
migration or movement patterns and
population dynamics) used in the
model, and that the model results must
be interpreted within the context of a
given species’ ecology.
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When reviewing the acoustic
exposure modeling results, it is also
important to understand that the
estimates of marine mammal sound
exposures are presented with
consideration of standard protective
measure operating procedures. The ROP
along with monitoring and mitigation
measures for the Keyport Range
Complex RDT&E activities, including
detection of marine mammals,
protective measures such as stand off
distances and delaying or halting
activities, and power down procedures
if marine mammals are detected within
one of the exclusion zones, are provided
below.
Because of the time delay between
pings, an animal encountering the sonar
will accumulate energy for only a few
sonar pings over the course of a few
minutes. Therefore, exposure to sonar
would be a short-term event,
minimizing any single animal’s
exposure to sound levels approaching
the harassment thresholds.
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Effects on Marine Mammal Habitat
The proposed extended area for the
Keyport Range Site is also critical
habitat of the Southern Resident killer
whales. The current Keyport Range Site
is outside the critical habitat area. There
are no other areas within the Keyport
Range Complex with extensions that are
specifically considered as important
physical habitat for marine mammals.
The prey of marine mammals are
considered part of their habitat. The
Navy’s DEIS for the Keyport Range
Complex RDT&E and range extension
activities contain a detailed discussion
of the potential effects to fish from
active acoustic sources. Below is a
summary of conclusions regarding those
effects.
Effects on Fish From Active Acoustic
Sources
The extent of data, and particularly
scientifically peer-reviewed data, on the
effects of high intensity sounds on fish
is limited. In considering the available
literature, the vast majority of fish
species studied to date are hearing
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generalists and cannot hear sounds
above 500 to 1,500 Hz (depending upon
the species), and, therefore, behavioral
effects on these species from higher
frequency sounds are not likely.
Moreover, even those fish species that
may hear above 1.5 kHz, such as a few
sciaenids and the clupeids (and
relatives), have relatively poor hearing
above 1.5 kHz as compared to their
hearing sensitivity at lower frequencies.
Therefore, even among the species that
have hearing ranges that overlap with
some mid- and high-frequency sounds,
it is likely that the fish will only
actually hear the sounds if the fish and
source are very close to one another.
Finally, since the vast majority of
sounds that are of biological relevance
to fish are below 1 kHz (e.g., Zelick et
al., 1999; Ladich and Popper, 2004),
even if a fish detects a mid- or highfrequency sound, these sounds will not
mask detection of lower frequency
biologically relevant sounds. Based on
the above information, there will likely
be few, if any, behavioral impacts on
fish.
Alternatively, it is possible that very
intense mid- and high frequency signals
could have a physical impact on fish,
resulting in damage to the swim bladder
and other organ systems. However, even
these kinds of effects have only been
shown in a few cases when the fish has
been very close to the source. Such
effects have never been indicated in
response to any Navy sonar. Moreover,
at greater distances (the distance clearly
would depend on the intensity of the
signal from the source) there appears to
be little or no impact on fish, and
particularly no impact on fish that do
not have a swim bladder or other air
bubble that would be affected by rapid
pressure changes.
Proposed Mitigation Measures
In order to issue an incidental take
authorization (ITA) under Section
101(a)(5)(A) of the MMPA, NMFS must
set forth the ‘‘permissible methods of
taking pursuant to such activity, and
other means of effecting the least
practicable adverse impact on such
species or stock and its habitat, paying
particular attention to rookeries, mating
grounds, and areas of similar
significance.’’ The National Defense
Authorization Act (NDAA) of 2004
amended the MMPA as it relates to
military-readiness activities and the
incidental take authorization process
such that ‘‘least practicable adverse
impact’’ shall include consideration of
personnel safety, practicality of
implementation, and impact on the
effectiveness of the ‘‘military readiness
activity.’’
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In addition, any mitigation measure
prescribed by NMFS should be known
to accomplish, have a reasonable
likelihood of accomplishing (based on
current science), or contribute to the
accomplishment of one or more of the
general goals listed below:
(a) Avoidance or minimization of
injury or death of marine mammals
wherever possible (goals b, c, and d may
contribute to this goal).
(b) A reduction in the numbers of
marine mammals (total number or
number at a biologically important time
or location) exposed to received levels
underwater active acoustic sources or
other activities expected to result in the
take of marine mammals (this goal may
contribute to a, above, or to reducing
harassment takes only).
(c) A reduction in the number of times
(total number or number at biologically
important time or location) individuals
would be exposed to received levels of
underwater active acoustic sources or
other activities expected to result in the
take of marine mammals (this goal may
contribute to a, above, or to reducing
harassment takes only).
(d) A reduction in the intensity of
exposures (either total number or
number at biologically important time
or location) to received levels of
underwater active acoustic sources
expected to result in the take of marine
mammals (this goal may contribute to a,
above, or to reducing the severity of
harassment takes only).
(e) A reduction in adverse effects to
marine mammal habitat, paying special
attention to the food base, activities that
block or limit passage to or from
biologically important areas, permanent
destruction of habitat, or temporary
destruction/disturbance of habitat
during a biologically important time.
(f) For monitoring directly related to
mitigation—an increase in the
probability of detecting marine
mammals, thus allowing for more
effective implementation of the
mitigation (shut-down zone, etc.).
NMFS worked with the Navy and
identified potential practicable and
effective mitigation measures, which
included a careful balancing of the
likely benefit of any particular measure
to the marine mammals with the likely
effect of that measure on personnel
safety, practicality of implementation,
and impact on the military readiness
activity. These mitigation measures are
listed below.
Proposed Mitigation Measures for Active
Acoustic Sources, Surface Operations
and Other Activities
Current protective measures known as
the ROP employed by the NAVSEA
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NUWC Keyport include applicable
training of personnel and
implementation of activity specific
procedures resulting in minimization
and/or avoidance of interactions with
protected resources and are provided
below.
(1) Range activities shall be conducted
in such a way as to ensure marine
mammals are not harassed or harmed by
human-caused events.
(2) Marine mammal observers are on
board ship during range activities. All
range personnel shall be trained in
marine mammal recognition. Marine
mammal observer training is normally
conducted by qualified organizations
such as NOAA/National Marine
Mammal Lab (NMML) on an as needed
basis.
(3) Vessels on a range use safety
lookouts during all hours of range
activities. Lookout duties include
looking for any and all objects in the
water, including marine mammals.
These lookouts are not necessarily
looking only for marine mammals. They
have other duties while aboard. All
sightings are reported to the Range
Officer in charge of overseeing the
activity.
(4) Visual surveillance shall be
accomplished just prior to all in-water
exercises. This surveillance shall ensure
that no marine mammals are visible
within the boundaries of the area within
which the test unit is expected to be
operating. Surveillance shall include, as
a minimum, monitoring from all
participating surface craft and, where
available, adjacent shore sites.
(5) The Navy shall postpone activities
until cetaceans (whales, dolphins, and
porpoises) leave the project area. When
cetaceans have been sighted in an area,
all range participants increase vigilance
and take reasonable and practicable
actions to avoid collisions and activities
that may result in close interaction of
naval assets and marine mammals.
Actions may include changing speed
and/or direction and are dictated by
environmental and other conditions
(e.g., safety, weather).
(6) An ‘‘exclusion zone’’ shall be
established and surveillance will be
conducted to ensure that there are no
marine mammals within this exclusion
zone prior to the commencement of
each in-water exercise. For cetaceans
(whales, dolphins, and porpoises), the
exclusion zone must be at least as large
as the entire area within which the test
unit may operate, and must extend at
least 1,000 yards (914.4 m) from the
intended track of the test unit. For
pinnipeds, the exclusion zone extends
out 100 yards (91 m) from the intended
track of the test unit.
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(7) Range craft shall not approach
within 100 yards (91 m) of marine
mammals and shall be followed to the
extent practicable considering human
and vessel safety priorities. All Navy
vessels and aircraft, including
helicopters, are expected to comply
with this directive. This includes
marine mammals ‘‘hauled-out’’ on
islands, rocks, and other areas such as
buoys.
(8) Passive acoustic monitoring shall
be utilized to detect marine mammals in
the area before and during activities,
especially when visibility is reduced.
(9) Procedures for reporting marine
mammal sightings on the NAVSEA
NUWC Keyport Range Complex shall be
promulgated, and sightings shall be
entered into the Range Operating
System and forwarded to NOAA/NMML
Platforms of Opportunity Program.
Research and Conservation Measures
for Marine Mammals
The Navy provides a significant
amount of funding and support for
marine research. The Navy provided
$26 million in Fiscal Year 2008 and
plans for $22 million in Fiscal Year
2009 to universities, research
institutions, Federal laboratories,
private companies, and independent
researchers around the world to study
marine mammals. Over the past five
years the Navy has funded over $100
million in marine mammal research.
The U.S. Navy sponsors seventy percent
of all U.S. research concerning the
effects of human-generated sound on
marine mammals and 50 percent of such
research conducted worldwide. Major
topics of Navy-supported research
include the following:
• Better understanding of marine
species distribution and important
habitat areas,
• Developing methods to detect and
monitor marine species before and
during training,
• Understanding the effects of sound
on marine mammals, sea turtles, fish,
and birds, and
• Developing tools to model and
estimate potential effects of sound.
The Navy’s Office of Naval Research
currently coordinates six programs that
examine the marine environment and
are devoted solely to studying the
effects of noise and/or the
implementation of technology tools that
will assist the Navy in studying and
tracking marine mammals. The six
programs are as follows:
• Environmental Consequences of
Underwater Sound,
• Non-Auditory Biological Effects of
Sound on Marine Mammals,
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• Effects of Sound on the Marine
Environment,
• Sensors and Models for Marine
Environmental Monitoring,
• Effects of Sound on Hearing of
Marine Animals, and
• Passive Acoustic Detection,
Classification, and Tracking of Marine
Mammals.
Furthermore, research cruises led by
NMFS and by academic institutions
have received funding from the Navy.
The Navy has sponsored several
workshops to evaluate the current state
of knowledge and potential for future
acoustic monitoring of marine
mammals. The workshops brought
together acoustic experts and marine
biologists from the Navy and other
research organizations to present data
and information on current acoustic
monitoring research efforts and to
evaluate the potential for incorporating
similar technology and methods on
instrumented ranges. However, acoustic
detection, identification, localization,
and tracking of individual animals still
requires a significant amount of research
effort to be considered a reliable method
for marine mammal monitoring. The
Navy supports research efforts on
acoustic monitoring and will continue
to investigate the feasibility of passive
acoustics as a potential mitigation and
monitoring tool.
Overall, the Navy will continue to
fund ongoing marine mammal research,
and is planning to coordinate long-term
monitoring/studies of marine mammals
on various established ranges and
operating areas. The Navy will continue
to research and contribute to university/
external research to improve the state of
the science regarding marine species
biology and acoustic effects. These
efforts include mitigation and
monitoring programs; data sharing with
NMFS and via the literature for research
and development efforts.
Long-Term Prospective Study
NMFS, with input and assistance
from the Navy and several other
agencies and entities, will perform a
longitudinal observational study of
marine mammal strandings to
systematically observe for and record
the types of pathologies and diseases
and investigate the relationship with
potential causal factors (e.g., sonar,
seismic, weather). The study will not be
a true ‘‘cohort’’ study, because we will
be unable to quantify or estimate
specific sonar or other sound exposures
for individual animals that strand.
However, a cross-sectional or
correlational analysis, a method of
descriptive rather than analytical
epidemiology, can be conducted to
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compare population characteristics, e.g.,
frequency of strandings and types of
specific pathologies between general
periods of various anthropogenic
activities and non-activities within a
prescribed geographic space. In the long
term study, we will more fully and
consistently collect and analyze data on
the demographics of strandings in
specific locations and consider
anthropogenic activities and physical,
chemical, and biological environmental
parameters. This approach in
conjunction with true cohort studies
(tagging animals, measuring received
sounds, and evaluating behavior or
injuries) in the presence of activities
and non-activities will provide critical
information needed to further define the
impacts of MTEs and other
anthropogenic and non-anthropogenic
stressors. In coordination with the Navy
and other federal and non-federal
partners, the comparative study will be
designed and conducted for specific
sites during intervals of the presence of
anthropogenic activities such as sonar
transmission or other sound exposures
and absence to evaluate demographics
of morbidity and mortality, lesions
found, and cause of death or stranding.
Additional data that will be collected
and analyzed in an effort to control
potential confounding factors include
variables such as average sea
temperature (or just season),
meteorological or other environmental
variables (e.g., seismic activity), fishing
activities, etc. All efforts will be made
to include appropriate controls (i.e., no
sonar or no seismic); environmental
variables may complicate the
interpretation of ‘‘control’’
measurements. The Navy and NMFS
along with other partners are evaluating
mechanisms for funding this study.
Proposed Monitoring Measures
In order to issue an incidental take
authorization (ITA) for an activity,
section 101(a)(5)(A) 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
LOAs 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.
Monitoring measures prescribed by
NMFS should accomplish one or more
of the following general goals:
(a) An increase in the probability of
detecting marine mammals, both within
the safety zone (thus allowing for more
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effective implementation of the
mitigation) and in general to generate
more data to contribute to the analyses
mentioned below.
(b) An increase in our understanding
of how many marine mammals are
likely to be exposed to levels of HFAS/
MFAS (or other stimuli) that we
associate with specific adverse effects,
such as behavioral harassment, TTS, or
PTS.
(c) An increase in our understanding
of how marine mammals respond to
HFAS/MFAS (at specific received
levels) or other stimuli expected to
result in take and how anticipated
adverse effects on individuals (in
different ways and to varying degrees)
may impact the population, species, or
stock (specifically through effects on
annual rates of recruitment or survival)
through any of the following methods:
• Behavioral observations in the
presence of HFAS/MFAS compared to
observations in the absence of sonar
(need to be able to accurately predict
received level and report bathymetric
conditions, distance from source, and
other pertinent information).
• Physiological measurements in the
presence of HFAS/MFAS compared to
observations in the absence of sonar
(need to be able to accurately predict
received level and report bathymetric
conditions, distance from source, and
other pertinent information), and/or
• Pre-planned and thorough
investigation of stranding events that
occur coincident to naval activities.
• Distribution and/or abundance
comparisons in times or areas with
concentrated HFAS/MFAS versus times
or areas without HFAS/MFAS.
(d) An increased knowledge of the
affected species.
(e) An increase in our understanding
of the effectiveness of certain mitigation
and monitoring measures.
With these goals in mind, the
following monitoring procedures for the
proposed Navy’s NAVSEA NUWC
Keyport Range Complex RDT&E and
range extension activities have been
worked out between NMFS and the
Navy. Keyport will conduct two special
surveys per year to monitor HFAS and
MFAS respectively. This will occur at
the DBRC Range site. This will include
visual surveys composed of vessel,
shore monitoring and passive acoustic
monitoring. Marine mammal observers
may be on range craft and/or on shore
side. NMFS and the Navy continue to
improve the plan and may modify the
monitoring plan based on input
received during the public comment
period.
Several monitoring techniques were
prescribed for other Navy activities
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related to sonar exercises (see
monitoring plan for Navy’s Hawaii
Range Complex; Navy, 2008). Every
known monitoring technique has
advantages and disadvantages that vary
temporally and spatially. Therefore, a
combination of techniques is proposed
to be used so that the detection and
observation of marine animals is
maximized. Monitoring methods
proposed during mission activity events
in the NAVSEA NUWC Keyport Range
Complex Study Area include a
combination of the following research
elements that would be used to collect
data for comprehensive assessment:
• Visual Surveys—Vessel, Shorebased, and Aerial (as applicable)
• Passive Acoustic Monitoring (PAM)
• Marine Mammal Observers (MMOs)
on Range craft
Visual Surveys
Visual surveys of marine animals can
provide detailed information about their
behavior, distribution, and abundance.
Baseline measurements and/or data for
comparison can be obtained before,
during and after mission activities.
Changes in behavior and geographical
distribution may be used to infer if and
how animals are impacted by sound. In
accordance with all safety
considerations, observations will be
maximized by working from all
available platforms: vessels, aircraft,
land and/or in combination. Shorebased (for inland waters), vessel and
aerial (as applicable) surveys may be
conducted from shore support, range
craft, Navy vessels, or contracted
vessels. Visual surveys will be
conducted during NAVSEA NUWC
Keyport range events which are
identified as being able to provide the
highest likelihood of success.
Vessel surveys are often preferred by
researchers because of their slow speed,
offshore survey ability, duration and
ability to more closely approach animals
under observation. They also result in
higher rate of species identification, the
opportunity to combine line transect
and mark-recapture methods of
estimating abundance, and collection of
oceanographic and other relevant data.
Vessels can be less expensive per unit
of time, but because of the length of
time to cover a given survey area, may
actually be more expensive in the long
run compared to aerial surveys (Dawson
et al., 2008). Changes in behavior and
geographical distribution may be used
to infer if and how animals are impacted
by sound. However, it should be noted
that animal reaction (reactive
movement) to the survey vessel itself is
possible (Dawson et al., 2008). Vessel
surveys typically do not allow for
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observation of animals below the ocean
surface (e.g. in the water column) as
compared to aerial surveys (DoN, 2008a;
Slooten et al., 2004).
NAVSEA NUWC Keyport will
conduct two special surveys per year to
monitor HFAS and MFAS respectively.
This will occur at the DBRC Range site.
The determination to monitor in the
DBRC area includes the following
reasoning: (1) It would provide the
highest amount of activity; (2) it is a
controlled environment; (3)
permanently bottom mounted
monitoring hydrophones are in place;
(4) most likely environment to get
accurate data; and (5) conducive to
excellent shore side observation.
For specified events, shore-based and
vessel surveys will be used 1 day prior
to and 1–2 days post activity. The
variation in the number of days after
allows for the detection of animals that
gradually return to an area, if they
indeed do change their distribution in
response to the associated events. DBRC
is a small area and animals are likely to
return more quickly than if the test were
in open ocean.
Surveys will include the range site
with special emphasis given to the
particular path of the test run. Passive
acoustic system (hydrophone or towed
array) would be used to determine if
marine mammals are in the area before
and/or after the event. When conducting
a particular survey, the survey team will
collect: (1) Species identification and
group size; (2) location and relative
distance from the acoustic source(s); (3)
the behavior of marine mammals,
including standard environmental and
oceanographic parameters; (4) date, time
and visual conditions associated with
each observation; (5) direction of travel
relative to the active acoustic source;
and (6) duration of the observation.
Animal sightings and relative distance
from a particular active acoustic source
will be used post-survey to determine
potential received energy (dB re 1 micro
Pa-sec). This data will be used, postsurvey, to estimate the number of
marine mammals exposed to different
received levels (energy based on
distance to the source, bathymetry,
oceanographic conditions and the type
and power of the acoustic source) and
their corresponding behavior.
Although photo-identification studies
are not typically a component of Navy
RDT&E activity monitoring surveys, the
Navy supports using the contracted
platforms to obtain opportunistic data
collection. Therefore, absent
classification issues any unclassified
digital photographs, if taken, of marine
mammals during visual surveys will be
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provided to local researchers for their
regional research if requested.
Marine Mammal Observer on Navy
Vessels
1. Shore-Based Surveys
All Keyport Range Complex operators
are trained by NOAA in marine
mammal identification. Additional use
of civilian biologists as Marine Mammal
Observers (MMOs) aboard range craft
and Navy vessels may be used to
research the effectiveness of Navy
marine observers, as well as for data
collection during other monitoring
surveys.
MMOs will be field-experienced
observers who are Navy biologists or
contracted observers. These civilian
MMOs will be placed alongside existing
Navy marine observers during a sub-set
of Keyport Range Complex RDT&E
activities. This can only be done on
certain vessels and observers may be
required to have security clearance.
NUWC Keyport may also use MMOs on
range craft during test events being
monitored. MMOs will not be placed
aboard Navy platforms for every Navy
testing event, but during specifically
identified opportunities deemed
appropriate for data collection efforts.
The events selected for MMO
participation will take into account
safety, logistics, and operational
concerns. Use of MMOs will verify Navy
marine observer sighting efficiency,
offer an opportunity for more detailed
species identification, provide an
opportunity to bring animal protection
awareness to the vessels’ crew, and
provide the opportunity for an
experienced biologist to collect data on
marine mammal behavior. Data
collected by the MMOs is anticipated to
assist the Navy with potential
improvements to marine observer
training as well as providing the marine
observers with a chance to gain
additional knowledge on marine
mammals.
Events selected for MMO
participation will be an appropriate fit
in terms of security, safety, logistics,
and compatibility with Keyport Range
Complex RDT&E activities. The MMOs
will not be part of the Navy’s formal
vessel reporting chain of command
during their data collection efforts, and
Navy marine observers will follow the
appropriate chain of command in
reporting marine mammal sightings.
Exceptions will be made if an animal is
observed by the MMO within the
shutdown zone and was not seen by the
Navy marine observer. The MMO will
inform the Navy marine observer of the
sighting so that appropriate action may
be taken by the chain of command. For
less biased data, it is recommended that
MMOs schedule their daily observations
A large number of test events in the
Keyport Range complex are conducted
in inland waters allowing for excellent
shore based surveillance opportunities.
When practicable, for test events
planned adjacent to nearshore areas,
where there are elevated topography or
coastal structures, shore-based visual
survey methods will be implemented
using binoculars or theodolite. These
methods have been proven valuable in
similar monitoring studies such as
ATOC and others (Frankel and Clark,
1998; Clark and Altman, 2006).
2. Vessel Surveys
Keyport Range Complex activities
conducted in the inland waters are
supported both from the shore
(described above) and from range craft.
The primary purpose of surveys
performed from these range craft will be
to document and monitor potential
behavioral effects of the mission
activities on marine mammals. As such,
parameters to be monitored for potential
effects are changes in the occurrence,
distribution, numbers, surface behavior,
and/or disposition (injured or dead) of
marine mammal species before, during
and after the mission activities. Postanalysis will focus on how the location,
speed and vector of the survey vessel
and the location and direction of the
sonar source (e.g., Navy surface vessel)
relates to the animal. Any other vessels
or aircraft observed in the area will also
be documented.
Passive Acoustic Monitoring
There are both benefits and
limitations to passive acoustic
monitoring (Mellinger et al., 2007).
Passive acoustic monitoring (PAM)
allows detection of marine mammals
that vocalize but may not be seen during
a visual survey. When interpreting data
collected from PAM, it is understood
that species specific results must be
viewed with caution because not all
animals within a given population are
calling, or may only be calling only
under certain conditions (Mellinger,
2007; ONR, 2007). The Keyport Range
Complex study area has advanced
features which allow for passive
acoustic monitoring. These
hydrophones are both permanently
bottom mounted, towed or over-theside. Subject matter experts are
available for detection and
identification of species type.
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to duplicate the Navy marine observers’
schedule.
Civilian MMOs will be aboard Navy
vessels involved in the study. As
described earlier, MMOs will meet and
adhere to necessary qualifications,
security clearance, logistics and safety
concerns. MMOs will monitor for
marine mammals from the same height
above water as the Navy marine
observers and as all visual survey teams,
they will collect the same data collected
by Navy marine observers, including but
not limited to: (1) Location of sighting;
(2) species (if not possible,
identification of whale or dolphin); (3)
number of individuals; (4) number of
calves present, if any; (5) duration of
sighting; (6) behavior of marine animals
sighted; (7) direction of travel; (8)
environmental information associated
with sighting event including Beaufort
sea state, wave height, swell direction,
wind direction, wind speed, glare,
percentage of glare, percentage of cloud
cover; and (9) when in relation to navy
exercises did the sighting occur.
In addition, the Navy is developing an
Integrated Comprehensive Monitoring
Program (ICMP) for marine species to
assess the effects of Keyport Range
Complex RDT&E activities on marine
species and investigate population
trends in marine species distribution
and abundance in locations where
Keyport Range Complex RDT&E
activities regularly occur. As part of the
ICMP, knowledge gained from other
Navy MMO monitored events will be
incorporated into NUWC Keyport
monitoring/mitigations as part of the
adaptive management approach.
The ICMP will provide the
overarching coordination that will
support compilation of data from rangespecific monitoring plans (e.g., Keyport
Range Complex plan) as well as Navy
funded research and development (R&D)
studies. The ICMP will coordinate the
monitoring program’s progress toward
meeting its goals and develop a data
management plan. The ICMP will be
evaluated annually to provide a matrix
for progress and goals for the following
year, and will make recommendations
on adaptive management for refinement
and analysis of the monitoring methods.
The primary objectives of the ICMP
are to:
• Monitor and assess the effects of
Navy activities on protected species;
• Ensure that data collected at
multiple locations is collected in a
manner that allows comparison between
and among different geographic
locations;
• Assess the efficacy and practicality
of the monitoring and mitigation
techniques;
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• Add to the overall knowledge-base
of marine species and the effects of
Navy activities on marine species.
The ICMP will be used both as: (1) A
planning tool to focus Navy monitoring
priorities (pursuant to ESA/MMPA
requirements) across Navy Range
Complexes and Exercises; and (2) an
adaptive management tool, through the
consolidation and analysis of the Navy’s
monitoring and watchstander data, as
well as new information from other
Navy programs (e.g., R&D), and other
appropriate newly published
information.
In combination with the adaptive
management component of the
proposed NAVSEA NUWC Keyport
Range Complex rule and the other
planned Navy rules (e.g., Atlantic Fleet
Active Sonar Training, Hawaii Range
Complex, and Southern California
Range Complex), the ICMP could
potentially provide a framework for
restructuring the monitoring plans and
allocating monitoring effort based on the
value of particular specific monitoring
proposals (in terms of the degree to
which results would likely contribute to
stated monitoring goals, as well as the
likely technical success of the
monitoring based on a review of past
monitoring results) that have been
developed through the ICMP
framework, instead of allocating based
on maintaining an equal (or
commensurate to effects) distribution of
monitoring effort across Range
complexes. For example, if careful
prioritization and planning through the
ICMP (which would include a review of
both past monitoring results and current
scientific developments) were to show
that a large, intense monitoring effort
would likely provide extensive, robust
and much-needed data that could be
used to understand the effects of sonar
throughout different geographical areas,
it may be appropriate to have other
Range Complexes dedicate money,
resources, or staff to the specific
monitoring proposal identified as ‘‘high
priority’’ by the Navy and NMFS, in lieu
of focusing on smaller, lower priority
projects divided throughout their home
Range Complexes. The ICMP will
identify:
• A means by which NMFS and the
Navy would jointly consider prior years’
monitoring results and advancing
science to determine if modifications
are needed in mitigation or monitoring
measures to better effect the goals laid
out in the Mitigation and Monitoring
sections of this proposed Keyport Range
Complex rule.
• Guidelines for prioritizing
monitoring projects
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• If, as a result of the Navy-NMFS
2011 Monitoring Workshop and similar
to the example described in the
paragraph above, the Navy and NMFS
decide it is appropriate to restructure
the monitoring plans for multiple ranges
such that they are no longer evenly
allocated (by Range Complex), but
rather focused on priority monitoring
projects that are not necessarily tied to
the geographic area addressed in the
rule, the ICMP will be modified to
include a very clear and unclassified
recordkeeping system that will allow
NMFS and the public to see how each
Range Complex/project is contributing
to all of the ongoing monitoring
(resources, effort, money, etc.).
coordinate with the Navy to modify or
add to the existing monitoring
requirements if the new data suggest
that the addition of a particular measure
would more effectively accomplish the
goals of monitoring laid out in this
proposed rule. The reporting
requirements associated with this
proposed rule are designed to provide
NMFS with monitoring data from the
previous year to allow NMFS to
consider the data in issuing annual
LOAs. NMFS and the Navy will meet
annually prior to LOA issuance to
discuss the monitoring reports, Navy
R&D developments, and current science
and whether mitigation or monitoring
modifications are appropriate.
Adaptive Management
Our understanding of the effects of
HFAS/MFAS on marine mammals is
still in its relative infancy, and yet the
science in this field is evolving fairly
quickly. These circumstances make the
inclusion of an adaptive management
component both valuable and necessary
within the context of 5-year regulations
for activities that have been associated
with marine mammal mortality in
certain circumstances and locations
(though not the Keyport Range Complex
Study Area). The use of adaptive
management will give NMFS the ability
to consider new data from different
sources to determine (in coordination
with the Navy), on an annual basis, if
new or modified mitigation or
monitoring measures are appropriate for
subsequent annual LOAs. Following are
some of the possible sources of
applicable data:
• Results from the Navy’s monitoring
from the previous year (either from the
Keyport Range Complex Study Area or
other locations).
• Results from specific stranding
investigations (either from the Keyport
Range Complex Study Area or other
locations, and involving coincident
Keyport Range Complex RDT&E or not
involving coincident use).
• Results from the research activities
associated with Navy’s HFAS/MFAS.
• Results from general marine
mammal and sound research (funded by
the Navy or otherwise).
• Any information which reveals that
marine mammals may have been taken
in a manner, extent or number not
authorized by these regulations and
subsequent Letters of Authorization.
Mitigation measures could be
modified or added if new data suggest
that such modifications would have a
reasonable likelihood of accomplishing
the goals of mitigation laid out in this
proposed rule and if the measures are
practicable. NMFS would also
Reporting
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In order to issue an ITA for an
activity, section 101(a)(5)(A) of the
MMPA states that NMFS must set forth
‘‘requirements pertaining to the
monitoring and reporting of such
taking.’’ Effective reporting is critical
both to monitoring compliance as well
as ensuring that the most value is
obtained from the required monitoring.
Some of the reporting requirements are
still in development and the final rule
may contain additional details not
contained in the proposed rule.
Additionally, proposed reporting
requirements may be modified,
removed, or added based on information
or comments received during the public
comment period.
Notification of Injured or Dead Marine
Mammals
Navy personnel will ensure through
proper chain of command that NMFS
(regional stranding coordinator) is
notified immediately (or as soon as
clearance procedures allow) if an
injured or dead marine mammal is
found during or shortly after, and in the
vicinity of, any Keyport Range Complex
RDT&E activities utilizing active
acoustic sources. The Navy will provide
NMFS with species or description of the
animal (s), the condition of the
animal(s) (including carcass condition if
the animal is dead), location, time of
first discovery, observed behaviors (if
alive), and photo or video (if available).
The Stranding Response Plan contains
more specific reporting requirements for
specific circumstances.
Annual Report
The Navy will submit its first annual
report to the Office of Protected
Resources, NMFS, no later than 120
days before the expiration of the LOA.
These reports will, at a minimum,
include the following information:
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• The estimated number of hours of
sonar and other operations involving
active acoustic sources, broken down by
source type.
• If possible, the total number of
hours of observation effort (including
observation time when sonar was not
operating).
• A report of all marine mammal
sightings (at any distance) to include,
when possible and to the best of their
ability, and if not classified:
—Species.
—Number of animals sighted.
—Location of marine mammal sighting.
—Distance of animal from any operating
sonar sources.
—Whether animal is fore, aft, port,
starboard.
—Direction animal is moving in relation
to source (away, towards, parallel).
—Any observed behaviors of marine
mammals.
• The status of any sonar sources
(what sources were in use) and whether
or not they were powered down or shut
down as a result of the marine mammal
observation.
• The platform that the marine
mammals were sighted from.
Keyport Range Complex Comprehensive
Report
The Navy will submit to NMFS a draft
report that analyzes and summarizes all
of the multi-year marine mammal
information gathered during test
activities involving active acoustic
sources for which annual reports are
required as described above. This report
will be submitted at the end of the
fourth year of the rule (anticipated to be
December 2013), covering activities that
have occurred through June 1, 2012. The
Navy will respond to NMFS comments
on the draft comprehensive report if
submitted within 3 months of receipt.
The report will be considered final after
the Navy has addressed NMFS’
comments, or three months after the
submittal of the draft if NMFS does not
comment by then.
Analysis and Negligible Impact
Determination
Pursuant to NMFS’ regulations
implementing the MMPA, an applicant
is required to estimate the number of
animals that will be ‘‘taken’’ by the
specified activities (i.e., takes by
harassment only, or takes by
harassment, injury, and/or death). This
estimate informs the analysis that NMFS
must perform to determine whether the
activity will have a ‘‘negligible impact’’
on the species or stock. Level B
(behavioral) harassment occurs at the
level of the individual(s) and does not
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assume any resulting population-level
consequences, though there are known
avenues through which behavioral
disturbance of individuals can result in
population-level effects. A negligible
impact finding is based on the lack of
likely adverse effects on annual rates of
recruitment or survival (i.e., populationlevel effects). An estimate of the number
of Level B harassment takes alone is not
enough information on which to base an
impact determination.
In addition to considering estimates of
the number of marine mammals that
might be ‘‘taken’’ through behavioral
harassment, NMFS must consider other
factors, such as the likely nature of any
responses (their intensity, duration,
etc.), the context of any responses
(critical reproductive time or location,
migration, etc.), as well as the number
and nature of estimated Level A takes,
the number of estimated mortalities, and
effects on habitat.
The Navy’s specified activities have
been described based on best estimates
of the planned RDT&E activities the
Navy would conduct within the
proposed NAVSEA NUWC Keyport
Range Complex Extension. The acoustic
sources proposed to be used in the
NAVSEA NUWC Keyport Range
Complex Extension are low intensity
and total proposed sonar operation
hours are under 1,570 hours. Taking the
above into account, along with the fact
that NMFS anticipates no mortalities
and injuries to result from the action,
the fact that there are no specific areas
of reproductive importance for marine
mammals recognized within the
Keyport Range Complex Extension
study area, the sections discussed
below, and dependent upon the
implementation of the proposed
mitigation measures, NMFS has
determined that Navy RDT&E activities
utilizing underwater acoustic sources
will have a negligible impact on the
affected marine mammal species and
stocks present in the proposed action
area.
Behavioral Harassment
As discussed in the Potential Effects
of Exposure of Marine Mammals to
HFAS/MFAS and illustrated in the
conceptual framework, marine
mammals can respond to HFAS/MFAS
in many different ways, a subset of
which qualifies as harassment. One
thing that the take estimates do not take
into account is the fact that most marine
mammals will likely avoid strong sound
sources to some extent. Although an
animal that avoids the sound source
will likely still be taken in some
instances (such as if the avoidance
results in a missed opportunity to feed,
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interruption of reproductive behaviors,
etc.) in other cases avoidance may result
in fewer instances of take than were
estimated or in the takes resulting from
exposure to a lower received level than
was estimated, which could result in a
less severe response. The Keyport Range
Complex application involves midfrequency and high frequency active
sonar operations shown in Table 2, and
none of the tests would involve
powerful tactical sonar such as the 53C
series MFAS. Therefore, any
disturbance to marine mammals
resulting from MFAS and HFAS in the
proposed Keyport Range Complex
RDT&E activities is expected to be
significantly less in terms of severity
when compared to major sonar exercises
(e.g., AFAST, HRC, SOCAL). In
addition, high frequency signals tend to
have more attenuation in the water
column and are more prone to lose their
energy during propagation. Therefore,
their zones of influence are much
smaller, thereby making it easier to
detect marine mammals and prevent
adverse effects from occurring.
There is little information available
concerning marine mammal reactions to
MFAS/HFAS. The Navy has only been
conducting monitoring activities since
2006 and has not compiled enough data
to date to provide a meaningful picture
of effects of HFAS/MFAS on marine
mammals, particularly in the Keyport
Range Complex Study Area. From the
four major training exercises (MTEs) of
HFAS/MFAS in the AFAST Study Area
for which NMFS has received a
monitoring report, no instances of
obvious behavioral disturbance were
observed by the Navy watchstanders in
the 700+ hours of effort in which 79
sightings of marine mammals were
made (10 during active sonar operation).
One cannot conclude from these results
that marine mammals were not harassed
from HFAS/MFAS, as a portion of
animals within the area of concern may
not have been seen (especially those
more cryptic, deep-diving species, such
as beaked whales or Kogia sp.) and some
of the non-biologist watchstanders
might not have had the expertise to
characterize behaviors. However, the
data demonstrate that the animals that
were observed did not respond in any
of the obviously more severe ways, such
as panic, aggression, or anti-predator
response.
In addition to the monitoring that will
be required pursuant to these
regulations and subsequent LOAs,
which is specifically designed to help
us better understand how marine
mammals respond to sound, the Navy
and NMFS have developed, funded, and
begun conducting a controlled exposure
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experiment with beaked whales in the
Bahamas.
Diel Cycle
As noted previously, many animals
perform vital functions, such as feeding,
resting, traveling, and socializing on a
diel cycle (24-hr cycle). Substantive
behavioral reactions to noise exposure
(such as disruption of critical life
functions, displacement, or avoidance of
important habitat) are more likely to be
significant if they last more than one
diel cycle or recur on subsequent days
(Southall et al., 2007). 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).
In the previous section, we discussed
the fact that potential behavioral
responses to HFAS/MFAS that fall into
the category of harassment could range
in severity. By definition, the takes by
Level B behavioral harassment involve
the disturbance of a marine mammal or
marine mammal stock in the wild by
causing disruption of natural behavioral
patterns (such as migration, surfacing,
nursing, breeding, feeding, or sheltering)
to a point where such behavioral
patterns are abandoned or significantly
altered. These reactions would,
however, be more of a concern if they
were expected to last over 24 hours or
be repeated in subsequent days.
Different sonar testing may not occur
simultaneously. Some of the marine
mammals in the Keyport Range
Complex Study Area are residents and
others would not likely remain in the
same area for successive days, it is
unlikely that animals would be exposed
to HFAS/MFAS at levels or for a
duration likely to result in a substantive
response that would then be carried on
for more than one day or on successive
days.
TTS
NMFS and the Navy have estimated
that individuals of some species of
marine mammals may sustain some
level of TTS from HFAS/MFAS
operations. As mentioned previously,
TTS can last from a few minutes to
days, be of varying degree, and occur
across various frequency bandwidths.
The TTS sustained by an animal is
primarily classified by three
characteristics:
• Frequency—Available data (of midfrequency hearing specialists exposed to
mid to high frequency sounds—Southall
et al., 2007) suggest that most TTS
occurs in the frequency range of the
source up to one octave higher than the
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source (with the maximum TTS at 1⁄2
octave above).
• Degree of the shift (i.e., how many
dB is the sensitivity of the hearing
reduced by)—generally, both the degree
of TTS and the duration of TTS will be
greater if the marine mammal is exposed
to a higher level of energy (which would
occur when the peak dB level is higher
or the duration is longer). The threshold
for the onset of TTS (> 6 dB) for Navy
sonars is 195 dB (SEL), which might be
received at distances of up to 275–500
m from the most powerful MFAS
source, the AN/SQS–53 (the maximum
ranges to TTS from other sources would
be less). An animal would have to
approach closer to the source or remain
in the vicinity of the sound source
appreciably longer to increase the
received SEL, which would be difficult
considering the marine observers and
the nominal speed of a sonar vessel (10–
12 knots). Of all TTS studies, some
using exposures of almost an hour in
duration or up to 217 dB SEL, most of
the TTS induced was 15 dB or less,
though Finneran et al. (2007) induced
43 dB of TTS with a 64-sec exposure to
a 20 kHz source (MFAS emits a 1-s ping
2 times/minute).
• Duration of TTS (Recovery time)—
see above. Of all TTS laboratory studies,
some using exposures of almost an hour
in duration or up to 217 dB SEL, almost
all recovered within 1 day (or less, often
in minutes), though in one study
(Finneran et al., 2007), recovery took 4
days.
Based on the range of degree and
duration of TTS reportedly induced by
exposures to non-pulse sounds of
energy higher than that to which freeswimming marine mammals in the field
are likely to be exposed during HFAS/
MFAS testing activities, it is unlikely
that marine mammals would sustain a
TTS from MFAS that alters their
sensitivity by more than 20 dB for more
than a few days (and the majority would
be far less severe). Also, for the same
reasons discussed in the Diel Cycle
section, and because of the short
distance within which animals would
need to approach the sound source, it is
unlikely that animals would be exposed
to the levels necessary to induce TTS in
subsequent time periods such that their
recovery were impeded. Additionally,
though the frequency range of TTS that
marine mammals might sustain would
overlap with some of the frequency
ranges of their vocalization types, the
frequency range of TTS from MFAS (the
source from which TTS would more
likely be sustained because the higher
source level and slower attenuation
make it more likely that an animal
would be exposed to a higher level)
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32299
would not usually span the entire
frequency range of one vocalization
type, much less span all types of
vocalizations.
Acoustic Masking or Communication
Impairment
As discussed above, it is also possible
that anthropogenic sound could result
in masking of marine mammal
communication and navigation signals.
However, masking only occurs during
the time of the signal (and potential
secondary arrivals of indirect rays),
versus TTS, which occurs continuously
for its duration. Masking effects from
HFAS/MFAS are expected to be
minimal. If masking or communication
impairment were to occur briefly, it
would be in the frequency range of
MFAS, which overlaps with some
marine mammal vocalizations; however,
it would likely not mask the entirety of
any particular vocalization or
communication series because the pulse
length, frequency, and duty cycle of the
HFAS/MFAS signal does not perfectly
mimic the characteristics of any marine
mammal’s vocalizations.
PTS, Injury, or Mortality
The Navy’s model estimated that no
marine mammal would be taken by
Level A harassment (injury, PTS
included) or mortality due to the low
intensity of the active sound sources
being used.
Based on the aforementioned
assessment, NMFS preliminarily
determines that there would be the
following number of takes: 11,283
harbor porpoises, 44 northern fur seals,
114 California sea lions, 14 northern
elephant seals, and 5,569 (5,468
Washington Inland Waters stock and
101 Oregon/Washington Coastal stock)
harbor seals at Level B harassment (TTS
and sub-TTS) as a result of the proposed
Keyport Range Complex RDT&E sonar
testing activities. These numbers do not
represent the number of individuals that
would be taken, since it’s most likely
that many individual marine mammals
would be taken multiple times.
However, under the worst case scenario
that each animal is taken only once, it
is expected that these take numbers
represent approximately 29.89%,
0.01%, 0.05%, 0.01%, 37.42%, and
0.41% of the Oregon/Washington
Coastal stock harbor porpoises, Eastern
Pacific stock northern fur seals, U.S.
stock California sea lions, California
breeding stock northern elephant seals,
Washington Inland Waters stock harbor
seals, and Oregon/Washington Coastal
stock harbor seals, respectively, in the
vicinity of the proposed Keyport Range
Complex Study Area (calculation based
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on NMFS 2007 U.S. Pacific Marine
Mammal Stock Assessments and 2007
U.S. Alaska Marine Mammal Stock
Assessments).
No Level A take (injury, PTS
included) or mortality would occur as
the result of the proposed RDT&E and
range extension activities for the
Keyport Range Complex.
Based on these analyses, NMFS has
preliminarily determined that the total
taking over the 5-year period of the
regulations and subsequent LOAs from
the Navy’s NAVSEA NUWCX Keyport
Range Complex RDT&E and range
extension activities will have a
negligible impact on the marine
mammal species and stocks present in
the Keyport Range Complex Study Area.
Subsistence Harvest of Marine
Mammals
NMFS has preliminarily determined
that the total taking of marine mammal
species or stocks from the Navy’s
mission activities in the Keyport Range
Complex study area would not have an
unmitigable adverse impact on the
availability of the affected species or
stocks for subsistence uses, since there
are no such uses in the specified area.
ESA
There are eight marine mammal
species/stocks over which NMFS has
jurisdiction that are listed as
endangered or threatened under the
ESA that could occur in the NAVSEA
NUWCX Keyport Range Complex study
area: Blue whales, fin whales, sei
whales, humpback whales, North
Pacific right whales, sperm whales,
Southern Resident killer whales, and
Steller sea lions. The Navy has begun
consultation with NMFS pursuant to
section 7 of the ESA, and NMFS will
also consult internally on the issuance
of regulations and LOAs under section
101(a)(5)(A) of the MMPA for mission
activities in the Keyport Range Complex
study area. Consultation will be
concluded prior to a determination on
the issuance of a final rule and an LOAs.
NEPA
The Navy is preparing an
Environmental Impact Statement (EIS)
for the proposed Keyport Range
Complex RDT&E and range extension
activities. A draft EIS was released for
public comment from September 12–
October 27, 2008 and is available at
https://www-keyport.kpt.nuwc.navy.mil.
NMFS is a cooperating agency (as
defined by the Council on
Environmental Quality (40 CFR 1501.6))
in the preparation of the EIS. NMFS has
reviewed the Draft EIS and will be
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working with the Navy on the Final EIS
(FEIS).
NMFS intends to adopt the Navy’s
FEIS, if adequate and appropriate, and
we believe that the Navy’s FEIS will
allow NMFS to meet its responsibilities
under NEPA for the issuance of the 5year regulations and LOAs (as
warranted) for mission activities in the
Keyport Range Complex study area. If
the Navy’s FEIS is not adequate, NMFS
would supplement the existing analysis
and documents to ensure that we
comply with NEPA prior to the issuance
of the final rule and LOA.
Preliminary Determination
Based on the analysis contained
herein of the likely effects of the
specified activity on marine mammals
and their habitat and dependent upon
the implementation of the mitigation
and monitoring measures, NMFS
preliminarily finds that the total taking
from NAVSEA NUWC Keyport Range
Complex RDT&E and range extension
activities utilizing active acoustic
sources in the NAVSEA NUWC Keyport
Range Complex study area will have a
negligible impact on the affected marine
mammal species or stocks. NMFS has
proposed regulations for these exercises
that prescribe the means of effecting the
least practicable adverse impact on
marine mammals and their habitat and
set forth requirements pertaining to the
monitoring and reporting of such taking.
Classification
This action does not contain a
collection of information requirements
for purposes of the Paperwork
Reduction Act.
This proposed rule has been
determined by the Office of
Management and Budget to be not
significant for purposes of Executive
Order 12866.
Pursuant to the Regulatory Flexibility
Act, the Chief Counsel for Regulation of
the Department of Commerce has
certified to the Chief Counsel for
Advocacy of the Small Business
Administration that this rule, if
adopted, would not have a significant
economic impact on a substantial
number of small entities. The RFA
requires Federal agencies to prepare an
analysis of a rule’s impact on small
entities whenever the agency is required
to publish a notice of proposed
rulemaking. However, a Federal agency
may certify, pursuant to 5 U.S.C. 605(b),
that the action will not have a
significant economic impact on a
substantial number of small entities.
The Navy is the sole entity that will be
affected by this proposed rulemaking,
not a small governmental jurisdiction,
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small organization or small business, as
defined by the RFA. This proposed
rulemaking authorizes the take of
marine mammals incidental to a
specified activity. The specified activity
defined in the proposed rule includes
the use of active acoustic sources during
RDT&E activities that are only
conducted by and for the U.S. Navy.
Additionally, the proposed regulations
are specifically written for ‘‘military
readiness’’ activities, as defined by the
Marine Mammal Protection Act, as
amended by the National Defense
Authorization Act, which means that
they cannot apply to small businesses.
Additionally, any requirements imposed
by a Letter of Authorization issued
pursuant to these regulations, and any
monitoring or reporting requirements
imposed by these regulations, will be
applicable only to the Navy. Because
this action, if adopted, would directly
affect the Navy and not a small entity,
NMFS concludes the action would not
result in a significant economic impact
on a substantial number of small
entities. Accordingly, no IRFA and none
has been prepared.
List of Subjects in 50 CFR Part 218
Exports, Fish, Imports, Incidental
take, Indians, Labeling, Marine
mammals, Navy, Penalties, Reporting
and recordkeeping requirements,
Seafood, Sonar, Transportation.
Dated: June 30, 2009.
James W. Balsiger,
Acting Assistant Administrator for Fisheries,
National Marine Fisheries Service.
For reasons set forth in the preamble,
50 CFR part 218 is proposed to be
amended as follows.
PART 218—REGULATIONS
GOVERNING THE TAKING AND
IMPORTING OF MARINE MAMMALS
1. The authority citation for part 218
continues to read as follows:
Authority: 16 U.S.C. 1361 et seq.
2. Subpart S is added to part 218 to
read as follows:
Subpart S—Taking Marine Mammals
Incidental to U.S. Navy Research,
Development, Test, and Evaluation
Activities in the Naval Sea System
Command Naval Undersea Warfare Center
Keyport Range Complex and the
Associated Proposed Extensions Study
Area
Sec.
218.170 Specified activity and specified
geographical area.
218.171 Permissible methods of taking.
218.172 Prohibitions.
218.173 Mitigation.
218.174 Requirements for monitoring and
reporting.
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218.175 Applications for Letters of
Authorization.
218.176 Letters of Authorization.
218.177 Renewal of Letters of Authorization
and adaptive management.
218.178 Modifications to Letters of
Authorization.
Subpart S—Taking Marine Mammals
Incidental to U.S. Navy Research,
Development, Test, and Evaluation
Activities in the Naval Sea System
Command (NAVSEA) Naval Undersea
Warfare Center (NUWC) Keyport Range
Complex and the Associated Proposed
Extensions Study Area
§ 218.170 Specified activity and specified
geographical area.
(a) Regulations in this subpart apply
only to the U.S. Navy for the taking of
marine mammals that occur in the area
outlined in paragraph (b) of this section
and that occur incidental to the
activities described in paragraph (c) of
this section.
(b) These regulations apply only to
the taking of marine mammals by the
Navy that occurs within the Keyport
Range Complex Action Area, which
includes the extended Keyport Range
Site, the extended DBRC Range
Complex (DBRC) Site, and the extended
Quinault Underwater Tracking Range
(QUTR) Site, as presented in the Navy’s
LOA application. The NAVSEA NUWC
Keyport Range Complex is divided into
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open ocean/offshore areas and in-shore
areas:
(1) Open Ocean Area—air, surface,
and subsurface areas of the NAVSEA
NUWC Keyport Range Complex
Extension that lie outside of 12 nautical
miles (nm) from land.
(2) Offshore Area—air, surface, and
subsurface ocean areas within 12 nm of
the Pacific Coast.
(3) In-shore—air, surface, and
subsurface areas within the Puget
Sound, Port Orchard Reach, Hood
Canal, and Dabob Bay.
(c) These regulations apply only to the
taking of marine mammals by the Navy
if it occurs incidental to the following
activities within the designated amounts
of use:
(1) Range Activities Using Active
Acoustic Devices:
(i) General range tracking: Narrow
frequency output between 10 to 100 kHz
with source levels (SL) between 195–
203 dB re 1 microPa-m.
(ii) UUV Tracking Systems: Operating
frequency of 10 to 100 kHz with SLs less
than 195 dB re 1 microPa-m at all range
sites.
(iii) Torpedo Sonars: Operating
frequency from 10 to 100 kHz with SL
under 233 dB re 1 microPa-m.
(iv) Range Targets and Special Test
Systems: 5 to 100 kHz frequency range
with a SL less than 195 dB re 1 microPam at the Keyport Range Site and SL less
than 238 dB re microPa-m at the DBRC
and QUTR sites.
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32301
(v) Special Sonars: Frequencies vary
from 100 to 2,500 kHz with SL less than
235 dB re 1 microPa-m.
(vi) Sonobuoys and Helicopter
Dipping Sonar: Operate at frequencies of
2 to 20 kHz with SLs of less than 225
dB re 1 microPa-m.
(vii) Side Scan Sonar: Multiple
frequencies typically at 100 to 700 kHz
with SLs less than 235 dB re 1 microPam.
(viii) Other Acoustic Sources:
(A) Acoustic Modems: Emit pulses at
frequencies from 10 to 300 kHz with SLs
less than 210 dB re 1 microPa-m.
(B) Target Simulators: Operate at
frequencies of 100 Hz to 10 kHz at
source levels of less than 170 dB re 1
microPa-m.
(C) Aids to Navigation: Operate at
frequencies of 70 to 80 kHz at SLs less
than 210 dB re 1 microPa-m.
(D) Subbottom Profilers: Operate at 2
to 7 kHz at SLs less than 210 dB re 1
microPa-m, and 35 to 45 kHz at SLs less
than 220 dB re 1 microPa-m.
(E) Surface Vessels, Submarines,
Torpedoes, and Other UUVs: Acoustic
energy from engines usually from 50 Hz
to 10 kHz at SLs less than 170 dB re 1
microPa-m.
(2) Increased Tempo and Activities
due to Range Extension: Proposed
annual range activities and operations
as listed in the following table:
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32302
Permissible methods of taking.
(a) Under Letters of Authorization
issued pursuant to §§ 216.106 and
218.176 of this chapter, the Holder of
the Letter of Authorization may
incidentally, but not intentionally, take
marine mammals within the area
described in § 218.170(b), provided the
activity is in compliance with all terms,
conditions, and requirements of these
regulations and the appropriate Letter of
Authorization.
(b) The activities identified in
§ 218.170(c) must be conducted in a
manner that minimizes, to the greatest
extent practicable, any adverse impacts
on marine mammals and their habitat.
(c) The incidental take of marine
mammals under the activities identified
in § 218.170(c) is limited to the
following species, by Level B
harassment only and the indicated
number of times:
(1) Harbor porpoise (Phocoena
phocoena)—56,415 (an average of
11,283 annually),
(2) Northern fur seal (Callorhinus
ursinus)—220 (an average of 44
annually);
(3) California sea lion (Zalophus
californianus)—570 (an average of 114
annually);
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(4) Northern elephant seal (Mirounga
angustirostris)—70 (an average of 14
annually);
(5) Harbor seal (Phoca vitulina
richardsi) (Washington Inland Waters
stock)—27,340 (an average of 5,468
annually); and
(6) Harbor seal (P. v. richardsi)
(Oregon/Washington Coastal stock)—
505 (an average of 101 annually);
§ 218.172
Prohibitions.
Notwithstanding takings
contemplated in § 218.171 and
authorized by a Letter of Authorization
issued under § 216.106 of this chapter
and § 218.176, no person in connection
with the activities described in
§ 218.170 may:
(a) Take any marine mammal not
specified in § 218.171(b);
(b) Take any marine mammal
specified in § 218.171(b) other than by
incidental take as specified in § 218.171
(b);
(c) Take a marine mammal specified
in § 218.171(b) if such taking results in
more than a negligible impact on the
species or stocks of such marine
mammal; or
(d) Violate, or fail to comply with, the
terms, conditions, and requirements of
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these regulations or a Letter of
Authorization issued under § 216.106 of
this chapter and § 218.176.
§ 218.173
Mitigation.
When conducting RDT&E activities
identified in § 218.170(c), the mitigation
measures contained in this subpart and
subsequent Letters of Authorization
issued under § 216.106 of this chapter
and § 218.176 must be implemented.
These mitigation measures include, but
are not limited to:
(a) Marine mammal observers
training:
(1) All range personnel shall be
trained in marine mammal recognition.
(2) Marine mammal observer training
shall be conducted by qualified
organizations approved by NMFS.
(b) Lookouts onboard vessels:
(1) Vessels on a range shall use
lookouts during all hours of range
activities.
(2) Lookout duties include looking for
marine mammals.
(3) All sightings of marine mammals
shall be reported to the Range Officer in
charge of overseeing the activity.
(c) Visual surveillance shall be
conducted just prior to all in-water
exercises.
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(1) Surveillance shall include, as a
minimum, monitoring from all
participating surface craft and, where
available, adjacent shore sites.
(2) When cetaceans have been sighted
in the vicinity of the operation, all range
participants increase vigilance and take
reasonable and practicable actions to
avoid collisions and activities that may
result in close interaction of naval assets
and marine mammals.
(3) Actions may include changing
speed and/or direction, subject to
environmental and other conditions
(e.g., safety, weather).
(d) An ‘‘exclusion zone’’ shall be
established and surveillance will be
conducted to ensure that there are no
marine mammals within this exclusion
zone prior to the commencement of
each in-water exercise.
(1) For cetaceans, the exclusion zone
shall extend out 1,000 yards (914.4 m)
from the intended track of the test unit.
(2) For pinnipeds, the exclusion zone
shall extend out 100 yards (91 m) from
the intended track of the test unit.
(e) Range craft shall not approach
within 100 yards (91 m) of marine
mammals, to the extent practicable
considering human and vessel safety
priorities. This includes marine
mammals ‘‘hauled-out’’ on islands,
rocks, and other areas such as buoys.
(f) In the event of a collision between
a Navy vessel and a marine mammal,
NUWC Keyport activities shall notify
immediately the Navy chain of
Command, which shall notify NMFS
immediately.
(g) Passive acoustic monitoring shall
be utilized to detect marine mammals in
the area before and during activities.
(h) Procedures for reporting marine
mammal sightings on the NAVSEA
NUWC Keyport Range Complex shall be
promulgated, and sightings shall be
entered into the Range Operating
System and forwarded to NOAA/NMML
Platforms of Opportunity Program.
§ 218.174 Requirements for monitoring
and reporting.
(a) The Holder of the Letter of
Authorization issued pursuant to
§ 216.106 of this chapter and § 218.176
for activities described in § 218.170(c) is
required to cooperate with the NMFS
when monitoring the impacts of the
activity on marine mammals.
(b) The Holder of the Authorization
must notify NMFS immediately (or as
soon as clearance procedures allow) if
the specified activity identified in
§ 218.170(c) is thought to have resulted
in the mortality or injury of any marine
mammals, or in any take of marine
mammals not identified or authorized in
§ 218.171(c).
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(c) The Navy must conduct all
monitoring and required reporting
under the Letter of Authorization,
including abiding by the NAVSEA
NUWC Keyport Range Complex
Monitoring Plan, which is incorporated
herein by reference, and which requires
the Navy to implement, at a minimum,
the monitoring activities summarized
below:
(1) Visual Surveys:
(i) The Holder of this Authorization
shall conduct a minimum of 2 special
visual surveys per year to monitor
HFAS and MFAS respectively at the
DBRC Range site.
(ii) For specified events, shore-based
and vessel surveys shall be used 1 day
prior to and 1–2 days post activity.
(A) Shore-based Surveys:
(1) Shore-based monitors shall
observe test events that are planned in
advance to occur adjacent to near shore
areas where there are elevated
topography or coastal structures, and
shall use binoculars or theodolite to
augment other visual survey methods.
(2) Shore-based surveys of the test
area and nearby beaches shall be
conducted for stranded marine animals
following nearshore events. If any
distressed, injured or stranded animals
are observed, an assessment of the
animal’s condition (alive, injured, dead,
or degree of decomposition) shall be
reported immediately to the Navy and
the information shall be transmitted
immediately to NMFS through the
appropriate chain of command.
(B) Vessel-based Surveys:
(1) Vessel-based surveys shall be
designed to maximize detections of
marine mammals near mission activity
event.
(2) Post-analysis shall focus on how
the location, speed and vector of the
range craft and the location and
direction of the sonar source (e.g., Navy
surface vessel) relates to the animal.
(3) Any other vessels or aircraft
observed in the area shall also be
documented.
(iii) Surveys shall include the range
site with special emphasis given to the
particular path of the test run. When
conducting a particular survey, the
survey team shall collect the following
information.
(A) Species identification and group
size;
(B) Location and relative distance
from the acoustic source(s);
(C) The behavior of marine mammals
including standard environmental and
oceanographic parameters;
(D) Date, time and visual conditions
associated with each observation;
(E) Direction of travel relative to the
active acoustic source; and
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32303
(F) Duration of the observation.
(iv) Animal sightings and relative
distance from a particular active
acoustic source shall be used postsurvey to determine potential received
energy (dB re 1 micro Pa-sec). This data
shall be used, post-survey, to estimate
the number of marine mammals
exposed to different received levels
(energy based on distance to the source,
bathymetry, oceanographic conditions
and the type and power of the acoustic
source) and their corresponding
behavior.
(2) Passive Acoustic Monitoring
(PAM):
(i) The Navy shall deploy a
hydrophone array in the Keyport Range
Complex Study Area for PAM.
(ii) The array shall be utilized during
the two special monitoring surveys in
DBRC as described in § 218.174(c)(1)(i).
(iii) The array shall have the
capability of detecting low-frequency
vocalizations (<1,000 Hz) for baleen
whales and relatively high frequency
(up to 30 kHz) for odontocetes.
(iv) Acoustic data collected from the
PAM shall be used to detect acoustically
active marine mammals as appropriate.
(3) Marine Mammal Observers on
range craft or Navy vessels:
(i) Navy Marine mammal observers
(NMMOs) may be placed on a range
craft or Navy platform during the event
being monitored.
(ii) The NMMO must possess
expertise in species identification of
regional marine mammal species and
experience collecting behavioral data.
(iii) NMMOs may be placed alongside
existing lookouts during the two
specified monitoring events as
described in § 218.174(c)(1)(i).
(iv) NMMOs shall inform the lookouts
of any marine mammal sighting so that
appropriate action may be taken by the
chain of command. NMMOs shall
schedule their daily observations to
duplicate the lookouts’ schedule.
(v) NMMOs shall observe from the
same height above water as the
lookouts, and they shall collect the same
data collected by lookouts listed in
§ 218.174(c)(1)(iii).
(d) The Navy shall complete an
Integrated Comprehensive Monitoring
Program (ICMP) Plan in 2009. This
planning and adaptive management tool
shall include:
(1) A method for prioritizing
monitoring projects that clearly
describes the characteristics of a
proposal that factor into its priority.
(2) A method for annually reviewing,
with NMFS, monitoring results, Navy
R&D, and current science to use for
potential modification of mitigation or
monitoring methods.
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(3) A detailed description of the
Monitoring Workshop to be convened in
2011 and how and when Navy/NMFS
will subsequently utilize the findings of
the Monitoring Workshop to potentially
modify subsequent monitoring and
mitigation.
(4) An adaptive management plan.
(5) A method for standardizing data
collection for NAVSEA NUWC Keyport
Range Complex Extension and across
range complexes.
(e) Notification of Injured or Dead
Marine Mammals—Navy personnel
shall ensure that NMFS (regional
stranding coordinator) is notified
immediately (or as soon as clearance
procedures allow) if an injured or dead
marine mammal is found during or
shortly after, and in the vicinity of, any
Navy training exercise utilizing
underwater explosive detonations. The
Navy shall provide NMFS with species
or description of the animal(s), the
condition of the animal(s) (including
carcass condition if the animal is dead),
location, time of first discovery,
observed behaviors (if alive), and photo
or video (if available).
(f) Annual Keyport Range Complex
Monitoring Plan Report—The Navy
shall submit a report annually on
December 1 describing the
implementation and results (through
September 1 of the same year) of the
Keyport Range Complex Monitoring
Plan. Data collection methods will be
standardized across range complexes to
allow for comparison in different
geographic locations. Although
additional information will also be
gathered, the NMMOs collecting marine
mammal data pursuant to the Keyport
Range Complex Monitoring Plan shall,
at a minimum, provide the same marine
mammal observation data required in
§ 218.174(c). The Keyport Range
Complex Monitoring Plan Report may
be provided to NMFS within a larger
report that includes the required
Monitoring Plan Reports from Keyport
Range Complex and multiple range
complexes.
(g) Keyport Range Complex 5-yr
Comprehensive Report—The Navy shall
submit to NMFS a draft comprehensive
report that analyzes and summarizes all
of the multi-year marine mammal
information gathered during tests
involving active acoustic sources for
which individual reports are required in
§ 218.174(d–f). This report will be
submitted at the end of the fourth year
of the rule (June 2013), covering
activities that have occurred through
September 1, 2013.
(h) The Navy shall respond to NMFS
comments and requests for additional
information or clarification on the
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Keyport Range Complex Extension
Comprehensive Report, the Annual
Keyport Range Complex Monitoring
Plan Report (or the multi-Range
Complex Annual Monitoring Report, if
that is how the Navy chooses to submit
the information) if submitted within 3
months of receipt. The report will be
considered final after the Navy has
addressed NMFS’ comments, or three
months after the submittal of the draft
if NMFS does not comment by then.
(i) In 2011, the Navy shall convene a
Monitoring Workshop in which the
Monitoring Workshop participants will
be asked to review the Navy’s
Monitoring Plans and monitoring results
and make individual recommendations
(to the Navy and NMFS) of ways of
improving the Monitoring Plans. The
recommendations shall be reviewed by
the Navy, in consultation with NMFS,
and modifications to the Monitoring
Plan shall be made, as appropriate.
§ 218.175 Applications for Letters of
Authorization.
To incidentally take marine mammals
pursuant to these regulations for the
activities identified in § 218.170(c), the
U.S. Navy must apply for and obtain
either an initial Letter of Authorization
in accordance with § 218.176 or a
renewal under § 218.177.
§ 218.176
Letters of Authorization.
(a) A Letter of Authorization, unless
suspended or revoked, will be valid for
a period of time not to exceed the period
of validity of this subpart, but must be
renewed annually subject to annual
renewal conditions in § 218.177.
(b) Each Letter of Authorization will
set forth:
(1) Permissible methods of incidental
taking;
(2) Means of effecting the least
practicable adverse impact on the
species, its habitat, and on the
availability of the species for
subsistence uses (i.e., mitigation); and
(3) Requirements for mitigation,
monitoring and reporting.
(c) Issuance and renewal of the Letter
of Authorization will be based on a
determination that the total number of
marine mammals taken by the activity
as a whole will have no more than a
negligible impact on the affected species
or stock of marine mammal(s).
§ 218.177 Renewal of Letters of
Authorization and adaptive management.
(a) A Letter of Authorization issued
under § 216.106 and § 218.176 for the
activity identified in § 218.170(c) will be
renewed annually upon:
(1) Notification to NMFS that the
activity described in the application
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submitted under § 218.175 shall be
undertaken and that there will not be a
substantial modification to the
described work, mitigation or
monitoring undertaken during the
upcoming 12 months;
(2) Timely receipt of the monitoring
reports required under § 218.174(b); and
(3) A determination by the NMFS that
the mitigation, monitoring and reporting
measures required under § 218.173 and
the Letter of Authorization issued under
§§ 216.106 and 218.176, were
undertaken and will be undertaken
during the upcoming annual period of
validity of a renewed Letter of
Authorization.
(b) If a request for a renewal of a
Letter of Authorization issued under
§§ 216.106 and 218.177 indicates that a
substantial modification to the
described work, mitigation or
monitoring undertaken during the
upcoming season will occur, the NMFS
will provide the public a period of 30
days for review and comment on the
request. Public comment on renewals of
Letters of Authorization are restricted
to:
(1) New cited information and data
indicating that the determinations made
in this document are in need of
reconsideration, and
(2) Proposed changes to the mitigation
and monitoring requirements contained
in these regulations or in the current
Letter of Authorization.
(c) A notice of issuance or denial of
a renewal of a Letter of Authorization
will be published in the Federal
Register.
(d) NMFS, in response to new
information and in consultation with
the Navy, may modify the mitigation or
monitoring measures in subsequent
LOAs if doing so creates a reasonable
likelihood of more effectively
accomplishing the goals of mitigation
and monitoring set forth in the preamble
of these regulations. Below are some of
the possible sources of new data that
could contribute to the decision to
modify the mitigation or monitoring
measures:
(1) Results from the Navy’s
monitoring from the previous year
(either from Keyport Range Complex
Study Area or other locations).
(2) Findings of the Monitoring
Workshop that the Navy will convene in
2011 (§ 218.174(i)).
(3) Compiled results of Navy funded
research and development (R&D) studies
(presented pursuant to the ICMP
(§ 218.174(d)).
(4) Results from specific stranding
investigations (either from the Keyport
Range Complex Study Area or other
locations).
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(5) Results from the Long Term
Prospective Study described in the
preamble to these regulations.
(6) Results from general marine
mammal and sound research (funded by
the Navy (described below) or
otherwise).
(7) Any information which reveals
that marine mammals may have been
taken in a manner, extent or number not
authorized by these regulations or
subsequent Letters of Authorization.
§ 218.178 Modifications to Letters of
Authorization.
(a) Except as provided in paragraph
(b) of this section and § 218.177(d), no
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substantive modification (including
withdrawal or suspension) to the Letter
of Authorization by NMFS, issued
pursuant to § 216.106 of this chapter
and § 218.176 and subject to the
provisions of this subpart shall be made
until after notification and an
opportunity for public comment has
been provided. For purposes of this
paragraph, a renewal of a Letter of
Authorization under § 218.177, without
modification (except for the period of
validity), is not considered a substantive
modification.
(b) If the Assistant Administrator
determines that an emergency exists
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32305
that poses a significant risk to the wellbeing of the species or stocks of marine
mammals specified in § 218.171(b), a
Letter of Authorization issued pursuant
to § 216.106 of this chapter and
§ 218.176 may be substantively
modified without prior notification and
an opportunity for public comment.
Notification will be published in the
Federal Register within 30 days
subsequent to the action.
[FR Doc. E9–15839 Filed 6–30–09; 4:15 pm]
BILLING CODE 3510–22–P
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Agencies
[Federal Register Volume 74, Number 128 (Tuesday, July 7, 2009)]
[Proposed Rules]
[Pages 32264-32305]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-15839]
[[Page 32263]]
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Part III
Department of Commerce
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National Oceanic and Atmospheric Administration
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50 CFR Part 218
Taking and Importing Marine Mammals; U.S. Navy's Research, Development,
Test, and Evaluation Activities Within the Naval Sea Systems Command
Naval Undersea Warfare Center Keyport Range Complex; Proposed Rule
Federal Register / Vol. 74, No. 128 / Tuesday, July 7, 2009 /
Proposed Rules
[[Page 32264]]
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DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
50 CFR Part 218
RIN 0648-AX11
Taking and Importing Marine Mammals; U.S. Navy's Research,
Development, Test, and Evaluation Activities Within the Naval Sea
Systems Command Naval Undersea Warfare Center Keyport Range Complex
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Proposed rule; request for comments.
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SUMMARY: NMFS has received a request from the U.S. Navy (Navy) for
authorization to take marine mammals incidental to the Navy's Research,
Development, Test, and Evaluation (RDT&E) activities within the Naval
Sea System Command (NAVSEA) Naval Undersea Warfare Center (NUWC)
Keyport Range Complex and the associated proposed extensions for the
period of September 2009 through September 2014. Pursuant to the Marine
Mammal Protection Act (MMPA), NMFS is proposing regulations to govern
that take and requesting information, suggestions, and comments on
these proposed regulations.
DATES: Comments and information must be received no later than August
6, 2009.
ADDRESSES: You may submit comments, identified by 0648-AX11, by any one
of the following methods:
Electronic Submissions: Submit all electronic public
comments via the Federal eRulemaking Portal https://www.regulations.gov
Hand delivery or mailing of paper, disk, or CD-ROM:
Comments should be addressed to Michael Payne, Chief, Permits,
Conservation and Education Division, Office of Protected Resources,
National Marine Fisheries Service, 1315 East-West Highway, Silver
Spring, MD 20910-3225.
Instructions: All comments received are a part of the public record
and will generally be posted to https://www.regulations.gov without
change. All personal identifying information (for example, name,
address, etc.) voluntarily submitted by the commenter may be publicly
accessible. Do not submit Confidential Business Information or
otherwise sensitive or protected information.
NMFS will accept anonymous comments (enter N/A in the required
fields if you wish to remain anonymous). Attachments to electronic
comments will be accepted in Microsoft Word, Excel, WordPerfect, or
Adobe PDF file formats only.
FOR FURTHER INFORMATION CONTACT: Shane Guan, Office of Protected
Resources, NMFS, (301) 713-2289, ext. 137.
SUPPLEMENTARY INFORMATION:
Availability
A copy of the Navy's application may be obtained by writing to the
address specified above (see ADDRESSES), telephoning the contact listed
above (see FOR FURTHER INFORMATION CONTACT), or visiting the internet
at: https://www.nmfs.noaa.gov/pr/permits/incidental.htm. The Navy's
Draft Environmental Impact Statement (DEIS) for the Keyport Range
Complex RDT&E and range extension activities was published on September
12, 2008, and may be viewed at https://www-keyport.kpt.nuwc.navy.mil.
NMFS participated in the development of the Navy's DEIS as a
cooperating agency under the National Environmental Policy Act (NEPA).
Background
Sections 101(a)(5)(A) and (D) of the MMPA (16 U.S.C. 1361 et seq.)
direct the Secretary of Commerce (Secretary) to allow, upon request,
the incidental, but not intentional taking of marine mammals by U.S.
citizens who engage in a specified activity (other than commercial
fishing) during periods of not more than five consecutive years each if
certain findings are made and regulations are issued or, if the taking
is limited to harassment, notice of a proposed authorization is
provided to the public for review.
Authorization shall be granted if NMFS finds that the taking will
have a negligible impact on the species or stock(s), will not have an
unmitigable adverse impact on the availability of the species or
stock(s) for subsistence uses, and if the permissible methods of taking
and requirements pertaining to the mitigation, monitoring and reporting
of such taking are set forth. NMFS has defined ``negligible impact'' in
50 CFR 216.103 as:
An impact resulting from the specified activity that cannot be
reasonably expected to, and is not reasonably likely to, adversely
affect the species or stock through effects on annual rates of
recruitment or survival.
The National Defense Authorization Act of 2004 (NDAA) (Public Law
108-136) removed the ``small numbers'' and ``specified geographical
region'' limitations in sections 101(a)(5)(A) and (D) and amended the
definition of ``harassment'' as it applies to a ``military readiness
activity'' to read as follows (Section 3(18)(B) of the MMPA):
(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].
Summary of Request
On May 15, 2008, NMFS received an application from the Navy
requesting authorization for the take of 5 species of marine mammals
incidental to the RDT&E activities within the NAVSEA NUWC Keyport Range
Complex Extension over the course of 5 years. These RDT&E activities
are classified as military readiness activities. On April 29, 2009,
NMFS received additional information and clarification on the Navy's
proposed NAVSEA NUWC Keyport Range Complex Extension RDT&E activities.
The Navy states that these RDT&E activities may cause various impacts
to marine mammal species in the proposed action area. The Navy requests
an authorization to take individuals of these marine mammals by Level B
Harassment. Please refer to Tables 6-23, 6-24, 6-25, and 6-26 of the
Navy's Letter of Authorization (LOA) application for detailed
information of the potential marine mammal exposures from the RDT&E
activities in the Keyport Range Complex Extension per year. However,
due to the proposed mitigation and monitoring measures and standard
range operating procedures in place, NMFS estimates that the take of
marine mammals is likely to be lower than the amount requested. NMFS
does not expect any marine mammals to be killed or injured as a result
of the Navy's proposed activities, and NMFS is not proposing to
authorize any injury or mortality incidental to the Navy's proposed
RDT&E activities within the Keyport Range Complex Extension.
Background of Navy Request
The Navy proposes to extend the NAVSEA NUWC Keyport Range Complex
in Washington State. The NAVSEA NUWC Keyport Range Complex has the
infrastructure to support RDT&E activities. Centrally located within
Washington State, the
[[Page 32265]]
NAVSEA NUWC Keyport Range Complex has extensive existing range assets
and capabilities. The NAVSEA NUWC Keyport Range Complex is composed of
Keyport Range Site, Dabob Bay Range Complex (DBRC) Site, and Quinault
Underwater Tracking Range (QUTR) Site (see Figure 1-1 of the Navy's LOA
application).
The goal of the Proposed Action is to extend the operational areas
of each range site. Extending the Range Complex operating areas outside
existing range boundaries will allow the Navy to support existing and
future range activities including evolving manned and unmanned vehicle
program needs in multiple marine environments. With the proposed
extension of the Keyport and QUTR range sites, the range sites could
support more activities, which include increases in the numbers of
tests and days of testing. No additional operational tempo is proposed
for the DBRC Site. Existing and evolving range activities applied for
in this LOA application include RDT&E and training of system
capabilities such as guidance, control, and sensor accuracy of manned
and unmanned vehicles in multiple marine environments (e.g., differing
depths, salinity levels, temperatures, sea states, etc.).
The range extension is necessary to provide adequate testing area
and volume (i.e., surface area and water depth) in multiple marine
environments. The extension enables the NUWC Keyport to fulfill its
mission of providing test and evaluation services in both surrogate and
simulated war-fighting environments for emerging manned and unmanned
vehicle program activities. Within the NAVSEA NUWC Keyport Range
Complex Extension, the NUWC Keyport activities include testing,
training, and evaluation of systems capabilities such as guidance,
control, and sensor accuracy of manned and unmanned vehicles in
multiple marine environments (e.g., differing depths, salinity levels,
temperatures, sea states, etc.).
NUWC Keyport consists of 340 acres (138 hectares [ha]) on the
shores of Liberty Bay and Port Orchard Reach (a.k.a. Port Orchard
Narrows), and is located adjacent to the town of Keyport, due west of
Seattle. NUWC Keyport, a part of NAVSEA, is the center for integrated
undersea warfare systems dependability, integrated mine and undersea
warfare supportability, and undersea vehicle maintenance and
engineering. It provides test and evaluation, in-service engineering,
maintenance, Fleet readiness, and industrial-based support for undersea
warfare systems, including RDT&E of torpedoes, unmanned vehicles,
sensors, targets, countermeasure systems, and acoustic systems.
The NAVSEA NUWC Keyport Range Complex is divided into open ocean/
offshore areas and in shore areas:
Open Ocean Area--air, surface, and subsurface areas of the
NAVSEA NUWC Keyport Range Complex that lie outside of 12 nautical miles
(nm) from land.
Offshore Area--air, surface, and subsurface ocean areas
within 12 nm of the Pacific Coast.
Inshore--air, surface, and subsurface areas within the
Puget Sound, Port Orchard Reach, Hood Canal, and Dabob Bay.
Keyport Range Site
Located adjacent to NUWC Keyport, this range provides approximately
1.5 square nautical miles (nm\2\) (5.1 square kilometers [km\2\]) of
shallow underwater testing, including in-shore shallow water sites and
a shallow lagoon to support integrated undersea warfare systems and
vehicle maintenance and engineering activities (see Figures 1-2 and 1-3
of the Navy's LOA application). The Navy has conducted underwater
testing at the Keyport Range Site since 1914. Underwater tracking of
test activities is accomplished by using temporary or portable range
equipment. The range is currently used an average of 6 times per year
for vehicle testing and a variety of boat and diver training
activities, each lasting 1-30 days. There may be several activities in
1 day. The range site also supports: (1) Detection, classification, and
localization of test objectives and (2) magnetics measurement programs.
Explosive warheads are not placed on test units or tested within the
Keyport Range Site.
DBRC Site
Currently, the DBRC Site assets include the Dabob Bay Military
Operating Area (MOA), the Hood Canal North and South MOAs adjacent to
Submarine Base (SUBASE) Bangor, and the Connecting Waters (see Figures
1-2 and 1-4 of the Navy's LOA application). The DBRC Site is the Navy's
premier location within the U.S. for RDT&E of underwater systems such
as torpedoes, countermeasures, targets, and ship systems. Primary
activities at the DBRC Site support proofing of underwater systems,
research and development test support, and Fleet training and tactical
evaluations involving aircraft, submarines, and surface ships. Tests
and evaluations of underwater systems, from the first prototype and
pre-production stages up through Fleet activities (inception to
deployment), ensure reliability and availability of underwater systems
and their Fleet components. As with the Keyport Range Site, there are
no explosive warheads tested or placed on test units.
The DBRC Site also supports acoustic/magnetic measurement programs.
These programs include underwater vehicle/ship noise/magnetic signature
recording, radiated sound investigations, and other acoustic
evaluations. In the course of these activities, various combinations of
aircraft, submarines, and surface ships are used as launch platforms.
Test equipment may also be launched or deployed from shore off a pier
or placed in the water by hand. NUWC Keyport currently conducts
activities within four underwater testing areas in the DBRC Site. These
areas are:
Dabob Bay MOA--a deep-water range in Jefferson County
approximately 14.5 nm\2\ (49.9 km\2\) in size. The acoustic tracking
space within the range is approximately 7.3 by 1.3 nm (13.5 by 2.4 km)
(9.5 nm\2\ [32.4 km\2\]) with a maximum depth of 600 ft (183 m). The
Dabob Bay MOA is the principal range and the only component of the DBRC
Site with extensive acoustic monitoring instrumentation installed on
the seafloor, allowing for object tracking, communications, passive
sensing, and target simulation.
Hood Canal MOAs--There are two deep-water operating areas
adjacent to SUBASE Bangor in Hood Canal: Hood Canal MOA South, which is
approximately 4.5 nm\2\ (15.4 km\2\) in size, and Hood Canal MOA North,
which is approximately 7.9 nm\2\ (27.0 km\2\) in size. Both areas have
an average depth of 200 ft (61 m). The Hood Canal MOAs are used for
vessel sensor accuracy tests and launch and recovery of test systems
where tracking is optional.
Connecting Waters--the portion of the Hood Canal that
connects the Dabob Bay MOA with the Hood Canal MOAs. The shortest
distance between the Dabob Bay MOA and Hood Canal MOA South by water is
approximately 5.8 nm\2\ (19.8 km\2\). Water depth in the Connecting
Waters is typically greater than 300 ft (91 m).
QUTR Site
The Navy has conducted underwater testing at the QUTR Site since
1981 and maintains a control center at the Kalaloch Ranger Station. As
at the other range sites, no explosive warheads are used at the QUTR
Site. The QUTR Site is a rectangular-shaped test area of about 48.3
nm\2\ (165.5 km\2\), located approximately 6.5 nm (12 km) off the
Pacific Coast at Kalaloch, Washington. It
[[Page 32266]]
lies within the boundaries of the Olympic Coast National Marine
Sanctuary (OCNMS).
The QUTR Site is instrumented to track surface vessels, submarines,
and various undersea vehicles. Bottom sensors are permanently mounted
on the sea floor for tracking and are maintained and configured by the
Navy. The sensors are connected to the shore via cables, which extend
under the beach to the bluffs and end at a Navy trailer in Kalaloch
(National Park Service [NPS] property). In addition, portable range
equipment may be set up prior to conducting various activities on the
range and removed after it is no longer needed. All communications are
sent back to NUWC Keyport for monitoring.
This range underlies a small portion (W-237A) of the larger
airspace unit W-237. This airspace complex comprises the northern
portion of the Pacific Northwest Ocean Surface/Subsurface Operating
Area (OPAREA), NOAA chart number 18500 (NOAA, 2006). Activities in this
airspace are scheduled and coordinated with Naval Air Station (NAS)
Whidbey Island and Commander Submarine Force, U.S. Pacific Fleet
(COMSUBPAC).
All range areas in the NAVSEA NUWC Keyport Range Complex Extension
include areas where marine mammals may be found. Range activities will
be conducted in the Keyport Site, the DBRC, and the QUTR Site. The
proposed annual usage at each site is listed in Table 1. This includes
tracking sonar systems, side-scan, and thermal propulsion systems.
Table 1--Projected Annual Days of Use by Range Site
----------------------------------------------------------------------------------------------------------------
QUTR site--
Keyport range DBRC site QUTR site-- surf zone
site offshore
----------------------------------------------------------------------------------------------------------------
Current......................................... 55 200 14 0
Proposed........................................ 60 200 16 30
----------------------------------------------------------------------------------------------------------------
Description of the Specified Activities
Typical activities conducted in the NAVSEA NUWC Keyport Range
Complex Extension on the three existing range sites primarily support
undersea warfare RDT&E program requirements, but they also support
general equipment test and military personnel training needs, including
Fleet activities. These activities involve mid- and high-frequency
acoustic sources with the potential to affect marine mammals that may
be present within the NAVSEA NUWC Keyport Range Complex Extension.
Current and proposed activities within the Keyport Range Complex
Extension are listed below:
Range Activities: Testing That Involves Active Acoustic Devices
A list of the primary active acoustic sources used within the
NAVSEA NUWC Keyport Range Complex with information on the frequency
bands is shown in Table 2. In this document, low frequency is defined
as below 1 kiloHertz (kHz), mid frequency is defined as between 1 kHz
and 10 kHz, and high frequency is defined as above 10 kHz.
Table 2--Primary Acoustic Sources Commonly Used Within the NAVSEA NUWC
Keyport Range Complex
------------------------------------------------------------------------
Maximum source
Source Frequency (kHz) level (dB re 1
[mu]Pa-m)
------------------------------------------------------------------------
Sonar:
General range tracking (at 10-100 195
Keyport Range Site)..........
General range tracking (at 10-100 203
DBRC and QUTR Sites).........
UUV tracking.................. 10-100 195
Torpedoes..................... 10-100 233
Range targets and special 5-100 195
tests (at Keyport Range Site)
Range targets and special 5-100 238
tests (at DBRC and QUTR
Sites).......................
Special sonars (e.g., UUV 100-2,500 235
payload).....................
Fleet aircraft--active 2-20 225
sonobuoys and helo-dipping
sonars.......................
Side-scan..................... 100-700 235
Other Acoustic Sources:
Acoustic modems............... 10-300 210
Target simulator.............. 0.1-10 170
Aid to navigation (range 70-80 210
equipment)...................
Sub-bottom profiler........... 2-7 210
35-45 220
Engine noise (surface vessels, 0.05-10 170
submarines, torpedoes, UUVs).
------------------------------------------------------------------------
(1) General Range Tracking
General range tracking on the instrumented ranges and portable
range sites have active output in relatively wide frequency bands.
Operating frequencies are 10 to 100 kHz. At the Keyport Range Site the
sound pressure level (SPL) of the source (source level) is a maximum of
195 dB re 1 [mu]Pa-m. At the DBRC and QUTR sites, the source level for
general range tracking is a maximum of 203 dB re 1 [mu]Pa-m.
(2) UUV Tracking Systems
UUV tracking systems operate at frequencies of 10 to 100 kHz with
maximum source levels of 195 dB re 1 [mu]Pa-m at all range sites.
(3) Torpedo Sonars
Torpedo sonars are used for several purposes including detection,
classification, and location and vary in frequency from 10 to 100 kHz.
The maximum source level of a torpedo sonar is 233 dB re 1 [mu]Pa-m.
[[Page 32267]]
(4) Range Targets and Special Tests
Range targets and special test systems are within the 5 to 100 kHz
frequency range at the Keyport Range Site with a maximum source level
of 195 dB re 1 [mu]Pa-m. At the DBRC and QUTR sites, the maximum source
level is 238 dB re 1 [mu]Pa-m.
(5) Special Sonars
Special sonars can be carried as a payload on a UUV, suspended from
a range craft, or set on or above the sea floor. These can vary widely
from 100 kHz to a very high frequency of 2,500 kHz for very short range
detection and classification. The maximum source level of these
acoustic sources is 235 dB re 1 [mu]Pa-m.
(6) Sonobuoys and Helicopter Dipping Sonar
Sonobuoys and helicopter dipping sonars are deployed from Fleet
aircraft and operate at frequencies of 2 to 20 kHz with maximum source
levels of 225 dB re 1 [mu]Pa-m. Dipping sonars are active or passive
devices that are lowered on cable by helicopters or surface vessels to
detect or maintain contact with underwater targets.
(7) Side Scan Sonar
Side-scan sonar is used for mapping, detection, classification, and
localization of items on the sea floor such as cabling, shipwrecks, and
mine shapes. It is high frequency typically 100 to 700 kHz using
multiple frequencies at one time with a very directional focus. The
maximum source level is 235 dB re 1 [mu]Pa-m. Side-scan and multibeam
sonar systems are towed or mounted on a test vehicle or ship.
(8) Other Acoustic Sources
Other acoustic sources may include acoustic modems, targets, aids
to navigation, subbottom profilers, and engine noise.
An acoustic modem is a communication device that transmits
an acoustically encoded signal from a source to a receiver. Acoustic
modems emit pulses from 10 to 300 kHz at source levels less than 210 dB
re 1 [mu]Pa-m.
Target simulators operate at frequencies of 100 Hertz (Hz)
(0.1 kHz) to 10 kHz at source levels of less than 170 dB re 1 [mu]Pa-m.
Aids to navigation transmit location data from ship to
shore and back to ship so the crew can have real-time detailed location
information. This is typical of the range equipment used in support of
testing. New aids to navigation can also be deployed and tested using
70 to 80 kHz at source levels less than 210 dB re 1 [mu]Pa-m.
Subbottom profilers are often commercial off-the-shelf
sonars used to determine characteristics of the sea bottom and
subbottom such as mud above bedrock or other rocky substrate. These
operate at 2 to 7 kHz at source levels less than 210 dB re 1 [mu]Pa-m,
and 35 to 45 kHz at less than 220 dB re 1 [mu]Pa-m.
There are many sources of engine noise including but not
limited to surface vessels, submarines, torpedoes, and other UUVs. The
acoustic energy generally ranges from 50 Hz to 10 kHz at source levels
less than 170 dB re 1 [mu]Pa-m. Targets, both mobile and stationary,
may simulate engine noise at these same frequencies.
Additionally, a variety of surface vessels operate active acoustic
depth sensors (fathometers) within the range sites, including Navy,
private, and commercial vessels. In some cases, one or more frequencies
are projected underwater. Bottom type, depth contours, and objects
(e.g., cables, sunken ships) can be located using this equipment. The
depth sensors used by NUWC Keyport are the same fathometers used by
commercial and recreational vessels for navigational safety. Because
these instruments are widely used and are not found to adversely impact
the human or natural environment, they are not analyzed further.
Range Activities: Testing That Involves Non-Acoustic Activities
(1) Magnetic
There are two types: (a) Magnetic sensors, and (b) magnetic
sources. Magnetic sensors are passive and do not have a magnetic field
associated with them. The sensors are bottom mounted, over the side
(stationary or towed) or can be integrated into a UUV. They are used to
sense the magnetic field of an object such as a surface vessel, a
submarine, or a buried target. Magnetic sources are used to represent
magnetic targets or are energized items such as power cables for energy
generators (e.g. tidal). Magnetic sources generate electromagnetic
fields (EMF). Evaluation of EMF (Navy 2008a) has shown that sources
(e.g. Organic Airborne and Surface Influence Sweep (OASIS)) used are
typically below 23 gauss (G) and are considered relatively minute
strength.
(2) Oceanographic Sensor
These sensors have been used historically to determine marine
characteristics such as conductivity, temperature, and pressure of
water to determine sound velocity in water. This provides information
about how sound will travel through the water. These sensors can be
deployed over the side from a surface craft, suspended in water, or
carried on a UUV.
(3) Laser Imaging Detection and Ranging (LIDAR)
Also known as light detection and ranging, LIDAR is used to measure
distance, speed, rotation, and chemical composition and concentration
of remote solid objects such as a ship or submerged object. LIDAR uses
the same principle as radar. The LIDAR instrument transmits short
pulses of laser light towards the target. The transmitted light
interacts with and is changed by the target. Some of this light is
reflected back to the instrument where it is analyzed. The change in
the properties of the light enables some property of the target to be
determined. The time it takes the light to travel to the target and
back to the LIDAR can be used to determine the distance to the target.
Since light attenuates rapidly in water, underwater LIDAR uses light in
the blue-green part of the spectrum as it attenuates the least. Common
civilian uses of LIDAR in the ocean include seabed mapping and fish
detection. All safety issues associated with the use of lasers are
evaluated for all applicable test activities within the range sites
according to Navy and Federal regulations. This bounds the intensity of
LIDAR used pursuant to this request to those systems that meet human
safety standards.
(4) Inert Mine Hunting and Inert Mine Clearing Exercises
Associated with testing, a series of inert mine shapes are set out
in a uniform or random pattern to test the detection, classification
and localization capability of the system under test. They are made
from plastic, metal, and concrete and vary in shape. An inert mine
shape can measure about 10 by 1.75 ft (3 by 0.5 m) and weigh about 800
lbs (362 kg). Inert mine shapes either sit on the bottom or are
tethered by an anchor to the bottom at various depths. Inert mine
shapes can be placed approximately 200-300 yards (183-274 m) apart
using a support craft and remain on the bottom until they need to be
removed. All major components of all inert mine systems used as
`targets' for inert mine hunting systems are removed within 2 years.
NMFS does not believe that those Range activities that involve non-
acoustic testing will have adverse impacts to marine mammals,
therefore,
[[Page 32268]]
they are not analyzed further and will not be covered under the
proposed rule.
Increased Activities Due to Range Extension
The proposed range extension would expand the geographic area for
all three range sites and increase the tempo of activities in the
Keyport and QUTR ranges sites. A detailed list of the proposed annual
range is provided in Table 3.
(1) Keyport Range Site
Range boundaries of the Keyport Range Site would be extended to the
north, east and south, increasing the size of the range from 1.5 nm\2\
to 3.2 nm\2\ (5.1 km\2\ to 11.0 km\2\). The average annual days of use
of the Keyport Range Site would increase from the current 55 days to 60
days.
(2) DBRC Site
The southern boundary of DBRC Site would be extended to the Hamma
Hamma River and its northern boundary would be extended to 1 nm (2 km)
south of the Hood Canal Bridge (Highway 104). This extension would
increase the size of the current operating area from approximately 32.7
nm\2\ (112.1 km\2\) to approximately 45.7 nm\2\ (150.8 km\2\) and would
afford a straight run of approximately 27.5 nm (50.9 km). There would
be no change in the number and types of activities from the existing
range activities at DBRC Site, and no increase in average annual days
of use due to the range extension at this site.
(3) QUTR Site
Range boundaries of QUTR Site would be extended to coincide with
the overlying special use airspace of W-237A plus a 7.8 nm\2\ (26.6
km\2\) surf zone at Pacific Beach. The total range area would increase
from approximately 48.3 nm\2\ (165.5 km\2\) to approximately 1,839.8
nm\2\ (6,310.2 km\2\). The average annual number of days of use for
offshore activities would increase from 14 days/year to 16 days/year in
the offshore area. The average annual days of use for surf-zone
activities would increase from 0 days/year to 30 days/year.
[GRAPHIC] [TIFF OMITTED] TP07JY09.002
Description of Marine Mammals in the Area of the Specified Activities
The information on marine mammals and their distribution and
density are based on the data gathered from NMFS, United States Fish
and Wildlife Service (USFWS) and recent references, literature searches
of search engines, peer review journals, and other technical reports,
to provide a regional context for each species. The data were compiled
from available sighting records, literature, satellite tracking, and
stranding and by-catch data.
A total of 24 cetacean species and subspecies and 5 pinniped
species are known to occur in Washington State waters; however, several
are seen only rarely. Seven of these marine mammal species are listed
as Federally-endangered under the Endangered Species Act (ESA) occur or
have the potential to occur in the proposed action area: blue whale
(Balaenoptera musculus), fin whale (B. physalus), Sei whale (B.
borealis), humpback whale (Megaptera novaengliae), north Pacific right
whale (Eubalaena japonica), sperm whale (Physeter macrocephalus), and
the southern resident population of
[[Page 32269]]
killer whales (Orcinus orca). The species, Steller sea lion (Eumetopias
jubatus), is listed as threatened under the ESA.
Survey data concerning the inland waters of Puget Sound are sparse.
There have been few comprehensive studies of marine mammals in inland
waters, and those that have occurred have focused on inland waters
farther north (Strait of Juan de Fuca, San Juan/Gulf Islands, Strait of
Georgia) (Osmek et al., 1998). Most published information focuses on
single species (e.g., harbor seals, Jeffries et al., 2003) or are stock
assessment reports published by NMFS (e.g., Carretta et al., 2008).
Survey data for the offshore waters of Washington State, including
the area of the QUTR Site, are somewhat better, particularly for
cetaceans. The NMFS conducted vessel surveys in the region in 1996 and
2001, which are summarized in Barlow (2003) and Appler et al. (2004).
Vessel surveys were again conducted by NMFS in summer 2005, and
included finer-scale survey lines within the OCNMS (Forney, 2007).
Cetacean densities from this most recent effort were used wherever
possible; older density values (2001 or 1996) were used when more
recent values were not available. Some cetacean densities (gray and
killer whale, harbor porpoise) were obtained from sources other than
the broad scale surveys indicated above and the methodologies of
deriving the densities are included in the Navy's LOA application.
Pinniped at-sea density is not often available because pinniped
abundance is most often obtained via shore counts of animals at known
rookeries and haulouts. Therefore, densities of pinnipeds were derived
differently from those of cetaceans. Several parameters were identified
from the literature, including area of stock occurrence, number of
animals (which may vary seasonally) and season, and those parameters
were then used to calculate density. Determining density in this manner
is risky as the parameters used usually contain error (e.g., geographic
range is not exactly known and needs to be estimated, abundance
estimates usually have large variances) and, as is true of all density
estimates, they assume that animals are always distributed evenly
within an area, which is likely rarely true. However, this remains one
of the few means available to determine at-sea density for pinnipeds.
Sea otters occur along the northern Washington coast. Density of
sea otters was published as animals/km, which was modified to provide
density per area. Since sea otters are under the U.S. Fish and Wildlife
Service jurisdiction, they are not considered in this document.
The following are brief descriptions of the temporal and spatial
distribution and abundance of marine mammals throughout the NAVSEA NUWC
Keyport Range Complex Extension.
Keyport Range Site
A total of five cetaceans and three pinnipeds are known to occur
within central Puget Sound, which encompasses the Keyport action area,
but several of these species have never been observed in Port Orchard
Narrows or in the action area (Table 4). Humpback whales, minke whales,
killer whales, and Steller sea lions are expected to be uncommon to
rare in southern Puget Sound and have never been seen in the Keyport
action area. Density estimates for these species are available for
Puget Sound as a whole, but since these species have never been
recorded or observed in the action area, the densities for the action
area are shown as ``0'' to reflect this. The proposed extension area of
the Keyport Range Site is listed as critical habitat for Southern
Resident killer whales. The current Keyport Range Site is outside the
critical habitat area.
[[Page 32270]]
[GRAPHIC] [TIFF OMITTED] TP07JY09.003
DBRC Site
Six cetaceans and three pinnipeds are known to occur or potentially
occur within the DBRC action area (Table 5). Density estimates for
these species are available for Puget Sound as a whole, but since these
species have never been recorded or observed in the action area, the
densities for the action area are shown as ``0'' to reflect this. There
is no designated or proposed critical habitat for marine mammals within
the DBRC action area.
[[Page 32271]]
[GRAPHIC] [TIFF OMITTED] TP07JY09.004
3.2.3 QUTR Site
The diversity of marine mammals that occur in QUTR is greater than
that in the Puget Sound ranges and is listed in Table 6.
BILLING CODE 3510-22-P
[[Page 32272]]
[GRAPHIC] [TIFF OMITTED] TP07JY09.005
[[Page 32273]]
[GRAPHIC] [TIFF OMITTED] TP07JY09.006
More detailed description of marine mammal density estimates within
the NAVSEA NUWC Keyport Range Complex Extension is provided in the
Navy's LOA application.
A Brief Background on Sound
An understanding of the basic properties of underwater sound is
necessary to comprehend many of the concepts and analyses presented in
this document. A summary is included below.
Sound is a wave of pressure variations propagating through a medium
(for the sonar considered in this proposed rule, the medium is marine
water). Pressure variations are created by compressing and relaxing the
medium. Sound measurements can be expressed in two forms: intensity and
pressure. Acoustic intensity is the average rate of energy transmitted
through a unit area in a specified direction and is expressed in watts
per square meter (W/m\2\). Acoustic intensity is rarely measured
directly, it is derived from ratios of pressures; the standard
reference pressure for underwater sound is 1 microPascal (microPa); for
airborne sound, the standard reference pressure is 20 microPa (Urick,
1983).
Acousticians have adopted a logarithmic scale for sound
intensities, which is denoted in decibels (dB). Decibel measurements
represent the ratio between a measured pressure value and a reference
pressure value (in this case 1 microPa or, for airborne sound, 20
microPa). The logarithmic nature of the scale means that each 10 dB
increase is a tenfold increase in power (e.g., 20 dB is a 100-fold
increase, 30 dB is a 1,000-fold increase). Humans perceive a 10-dB
increase in noise as a doubling of sound level, or a 10 dB decrease in
noise as a halving of sound level. The term ``sound pressure level''
implies a decibel measure and a reference pressure that is used as the
denominator of the ratio. Throughout this document, NMFS uses 1 microPa
as a standard reference pressure unless noted otherwise.
It is important to note that decibels underwater and decibels in
air are not the same and cannot be directly compared. To estimate a
comparison between sound in air and underwater, because of the
different densities of air and water and the different decibel
standards (i.e., reference pressures) in water and air, a sound with
the same intensity (i.e., power) in air and in water would be
approximately 61.5 dB lower in air. Thus, a sound that is 160 dB loud
underwater would have the same approximate effective intensity as a
sound that is 98.5 dB loud in air.
Sound frequency is measured in cycles per second, or Hertz
(abbreviated Hz), and is analogous to musical pitch; high-pitched
sounds contain high frequencies and low-pitched sounds contain low
frequencies. Natural sounds in the ocean span a huge range of
frequencies: from earthquake noise at 5 Hz to harbor porpoise clicks at
150,000 Hz (150 kHz). These sounds are so low or so high in pitch that
humans cannot even hear them; acousticians call these infrasonic and
ultrasonic sounds, respectively. A single sound may be made up of many
different frequencies together. Sounds made up of only a small range of
frequencies are called ``narrowband'', and sounds with a broad range of
frequencies are called ``broadband''; airguns are an example of a
broadband sound source and tactical sonars are an example of a
narrowband sound source.
When considering the influence of various kinds of sound on the
marine environment, it is necessary to understand that different kinds
of marine life are sensitive to different frequencies of sound. Based
on available behavioral data, audiograms derived using auditory evoked
potential, anatomical modeling, and other data, Southall et al. (2007)
designated ``functional hearing groups'' and estimated the lower and
upper frequencies of functional hearing of the groups. Further, the
frequency range in which each group's hearing is estimated as being
most sensitive is represented in the flat part of the M-weighting
functions developed for each group. The functional groups and the
associated frequencies are indicated below:
Low frequency cetaceans (13 species of mysticetes):
Functional hearing is estimated to occur between approximately 7 Hz and
22 kHz.
Mid-frequency cetaceans (32 species of dolphins, six
species of larger toothed whales, and 19 species of beaked and
bottlenose whales): Functional hearing is estimated to occur between
approximately 150 Hz and 160 kHz.
High frequency cetaceans (eight species of true porpoises,
six species of river dolphins, Kogia, the franciscana, and four species
of cephalorhynchids): Functional hearing is estimated to occur between
approximately 200 Hz and 180 kHz.
Pinnipeds in Water: Functional hearing is estimated to
occur between approximately 75 Hz and 75 kHz, with the greatest
sensitivity between approximately 700 Hz and 20 kHz.
Pinnipeds in Air: Functional hearing is estimated to occur
between approximately 75 Hz and 30 kHz.
Because ears adapted to function underwater are physiologically
different from human ears, comparisons using decibel measurements in
air would still not be adequate to describe the effects of a sound on a
cetacean. When sound travels away from its source, its loudness
decreases as the distance from the source increases (propagation).
Thus, the loudness of a sound at its source is higher than the loudness
of that same sound a kilometer distant. Acousticians often refer to the
loudness of a sound at its source (typically measured one meter from
the source) as the source level and the loudness of sound elsewhere as
the received level. For example, a humpback whale three kilometers from
an airgun that has a source level of 230 dB may only be
[[Page 32274]]
exposed to sound that is 160 dB loud, depending on how the sound
propagates. As a result, it is important not to confuse source levels
and received levels when discussing the loudness of sound in the ocean.
As sound travels from a source, its propagation in water is
influenced by various physical characteristics, including water
temperature, depth, salinity, and surface and bottom properties that
cause refraction, reflection, absorption, and scattering of sound
waves. Oceans are not homogeneous and the contribution of each of these
individual factors is extremely complex and interrelated. The physical
characteristics that determine the sound's speed through the water will
change with depth, season, geographic location, and with time of day
(as a result, in actual sonar operations, crews will measure oceanic
conditions, such as sea water temperature and depth, to calibrate
models that determine the path the sonar signal will take as it travels
through the ocean and how strong the sound signal will be at a given
range along a particular transmission path). As sound travels through
the ocean, the intensity associated with the wavefront diminishes, or
attenuates. This decrease in intensity is referred to as propagation
loss, also commonly called transmission loss.
Metrics Used in This Document
This section includes a brief explanation of the two sound
measurements (sound pressure level (SPL) and sound exposure level
(SEL)) frequently used in the discussions of acoustic effects in this
document.
SPL
Sound pressure is the sound force per unit area, and is usually
measured in microPa, where 1 Pa is the pressure resulting from a force
of one newton exerted over an area of one square meter. SPL is
expressed as the ratio of a measured sound pressure and a reference
level. The commonly used reference pressure level in underwater
acoustics is 1 microPa, and the units for SPLs are dB re: 1 microPa.
SPL (in dB) = 20 log (pressure/reference pressure)
SPL is an instantaneous measurement and can be expressed as the
peak, the peak-peak, or the root mean square (rms). Root mean square,
which is the square root of the arithmetic average of the squared
instantaneous pressure values, is typically used in discussions of the
effects of sounds on vertebrates. All references to SPL in this
document refer to the root mean square. SPL does not take the duration
of a sound into account. SPL is the applicable metric used in the risk
continuum, which is used to estimate behavioral harassment takes (see
Level B Harassment Risk Function (Behavioral Harassment) Section).
SEL
SEL is an energy metric that integrates the squared instantaneous
sound pressure over a stated time interval. The units for SEL are dB
re: 1 microPa\2\-s.
SEL = SPL + 10log (duration in seconds)
As applied to tactical sonar, the SEL includes both the SPL of a
sonar ping and the total duration. Longer duration pings and/or pings
with higher SPLs will have a higher SEL. Surface-ship hull-mounted
sonars, known as tactical sonars, are not used by NAVSEA NUWC Keyport.
If an animal is exposed to multiple pings, the SEL in each individual
ping is summed to calculate the total SEL. The total SEL depends on the
SPL, duration, and number of pings received. The thresholds that NMFS
uses to indicate the received levels at which the onset of temporary
threshold shift (TTS) and permanent threshold shift (PTS) in hearing
are likely to occur are expressed in SEL.
Potential Impacts to Marine Mammal Species
The following sections discuss the potential effects from noise
related to active acoustic devices that would be used in the proposed
Keyport Range Complex Extension.
For activities involving active acoustic sources such as tactical
sonar, NMFS's analysis identifies the probability of lethal responses,
physical trauma, sensory impairment (permanent and temporary threshold
shifts and acoustic masking), physiological responses (particular
stress responses), behavioral disturbance (that rises to the level of
harassment), and social responses that would be classified as
behavioral harassment or injury and/or would be likely to adversely
affect the species or stock through effects on annual rates of
recruitment or survival. It should be noted that the description below
is based on more powerful mid-frequency active sonar (MFAS) used on
surface ships. The NAVSEA NUWC Keyport Range does not utilize these
sources in RDT&E activities. Many of these severe effects (e.g.,
mortality, acoustically mediated bubble growth, and stranding) are not
likely to occur for acoustic sources used in the proposed Keyport Range
activities, as shown in Estimated Takes of Marine Mammals section.
Direct Physiological Effects
Based on the literature, there are two basic ways that MFAS might
directly result in physical trauma or damage: Noise-induced loss of
hearing sensitivity (more commonly-called ``threshold shift'') and
acoustically mediated bubble growth. Separately, an animal's behavioral
reaction to an acoustic exposure might lead to physiological effects
that might ultimately lead to injury or death, which is discussed later
in the Stranding section.
Threshold Shift (Noise-Induced Loss of Hearing)
When animals exhibit reduced hearing sensitivity (i.e., sounds must
be louder for an animal to recognize them) following exposure to a
sufficiently intense sound, it is referred to as a noise-induced
threshold shift (TS). An animal can experience temporary threshold
shift (TTS) or permanent threshold shift (PTS). TTS can last from
minutes or hours to days (i.e., there is recovery), occurs in specific
frequency ranges (i.e., an animal might only have a temporary loss of
hearing sensitivity between the frequencies of 1 and 10 kHz)), and can
be of varying amounts (for example, an animal's hearing sensitivity
might be reduced by only 6 dB or reduced by 30 dB). PTS is permanent
(i.e., there is no recovery), but as with TTS occurs in a specific
frequency range and amount.
The following physiological mechanisms are thought to play a role
in inducing auditory TSs: Effects to sensory hair cells in the inner
ear that reduce their sensitivity, modification of the chemical
environment within the sensory cells, residual muscular activity in the
middle ear, displacement of certain inner ear membranes, increased
blood flow, and post-stimulatory reduction in both efferent and sensory
neural output (Southall et al., 2007). The amplitude, duration,
frequency, temporal pattern, and energy distribution of sound exposure
all affect the amount of associated TS and the frequency range in which
it occurs. As amplitude and duration of sound exposure increase, so,
generally, does the amount of TS. For continuous sounds, exposures of
equal energy (the same SEL) will lead to approximately equal effects.
For intermittent sounds, less TS will occur than from a continuous
exposure with the same energy (some recovery will occur between
exposures) (Kryter et al., 1966; Ward, 1997). For example, one short
but loud (higher SPL) sound exposure may induce the same impairment as
one
[[Page 32275]]
longer but softer sound, which in turn may cause more impairment than a
series of several intermittent softer sounds with the same total energy
(Ward, 1997). Additionally, though TTS is temporary, very prolonged
exposure to sound strong enough to elicit TTS, or shorter-term exposure
to sound levels well above the TTS threshold, can cause PTS, at least
in terrestrial mammals (Kryter, 1985) (although in the case of MFAS,
animals are not expected to be exposed to levels high enough or
durations long enough to result in PTS).
PTS is considered auditory injury (Southall et al., 2007).
Irreparable damage to the inner or outer cochlear hair cells may cause
PTS, however, other mechanisms are also involved, such as exceeding the
elastic limits of certain tissues and membranes in the middle and inner
ears and resultant changes in the chemical composition of the inner ear
fluids (Southall et al., 2007).
Although the published body of scientific literature contains
numerous theoretical studies and discussion papers on hearing
impairments that can occur with exposure to a loud sound, only a few
studies provide empirical information on the levels at which noise-
induced loss in hearing sensitivity occurs in nonhuman animals. For
cetaceans, published data are limited to a captive bottlenose dolphin
and beluga whale (Finneran et al., 2000, 2002b, 2005a; Schlundt et al.,
2000; Nachtigall et al., 2003, 2004).
Marine mammal hearing plays a critical role in communication with
conspecific, and interpreting environmental cues for purposes such as
predator avoidance and prey capture. Depending on the frequency range
of TTS degree (dB), duration, and frequency range of TTS, and the
context in which it is experienced, TTS can have effects on marine
mammals ranging from discountable to serious (similar to those
discussed in auditory masking, below). For example, a marine mammal may
be able to readily compensate for a brief, relatively small amount of
TTS in a non-critical frequency range that takes place during a time
when the animal is traveling through the open ocean, where ambient
noise is lower and there are not as many competing sounds present.
Alternatively, a larger amount and longer duration of TTS sustained
during time when communication is critical for successful mother/calf
interactions could have more serious impacts. Also, depending on the
degree and frequency range, the effects of PTS on an animal could range
in severity, although it is considered generally more serious because
it is a long term condition. Of note, reduced hearing sensitivity as a
simple function of development and aging has been observed in marine
mammals, as well as humans and other taxa (Southall et al., 2007), so
we can infer that strategies exist for coping with this condition to
some degree, though likely not without cost. There is no empirical
evidence that exposure to MFAS can cause PTS in any marine mammals;
instead the probability of PTS has been inferred from studies of TTS
(see Richardson et al., 1995).
Acoustically Mediated Bubble Growth
One theoretical cause of injury to marine mammals is rectified
diffusion (Crum and Mao, 1996), the process of increasing the size of a
bubble by exposing it to a sound field. This process could be
facilitated if the environment in which the ensonified bubbles exist is
supersaturated with gas. Repetitive diving by marine mammals can cause
the blood and some tissues to accumulate gas to a greater degree than
is supported by the surrounding environmental pressure (Ridgway and
Howard, 1979). The deeper and longer dives of some marine mammals (for
example, beaked whales) are theoretically predicted to induce greater
supersaturation (Houser et al., 2001b). If rectified diffusion were
possible in marine mammals exposed to high-level sound, conditions of
tissue supersaturation could theoretically speed the rate and increase
the size of bubble growth. Subsequent effects due to tissue trauma and
emboli would presumably mirror those observed in humans suffering from
decompression sickness.
It is unlikely that the short duration of sonar pings would be long
enough to drive bubble growth to any substantial size, if such a
phenomenon occurs. Recent work conducted by Crum et al. (2005)
demonstrated the possibility of rectified diffusion for short duration
signals, but at sound exposure levels and tissue saturation levels that
are improbable to occur in a diving marine mammal. However, an
alternative but related hypothesis has also been suggested: Stable
bubbles could be destabilized by high-level sound exposures such that
bubble growth then occurs through static diffusion of gas out of the
tissues. In such a scenario the marine mammal would need to be in a
gas-supersaturated state for a long enough period of time for bubbles
to become of a problematic size. Yet another hypothesis (decompression
sickness) has speculated that rapid ascent to the surface following
exposure to a startling sound might produce tissue gas saturation
sufficient for the evolution of nitrogen bubbles (Jepson et al., 2003;
Fernandez et al., 2005). In this scenario, the rate of ascent would
need to be sufficiently rapid to compromise behavioral or physiological
protections against nitrogen bubble formation. Collectively, these
hypotheses can be referred to as ``hypotheses of acoustically mediated
bubble growth.''
Although theoretical predictions suggest the possibility for
acoustically mediated bubble growth, there is considerable disagreement
among scientists as to its likelihood (Piantadosi and Thalmann, 2004;
Evans and Miller, 2003). Crum and Mao (1996) hypothesized that received
levels would have to exceed 190 dB in order for there to be the
possibility of significant bubble growth due to supersaturation of
gases in the blood (i.e., rectified diffusion). More recent work
conducted by Crum et al. (2005) demonstrated the possibility of
rectified diffusion for short duration signals, but at SELs and tissue
saturation levels that are highly improbable to occur in diving marine
mammals. To date, Energy Levels (ELs) predicted to cause in vivo bubble
formation within diving cetaceans have not been evaluated (NOAA,
2002b). Although it has been argued that traumas from some recent
beaked whale strandings are consistent with gas emboli and bubble-
induced tissue separations (Jepson et al., 2003), there is no
conclusive evidence of this. However, Jepson et al. (2003, 2005) and
Fernandez et al. (2004, 2005) concluded that in vivo bubble formation,
which may be exacerbated by deep, long duration, repetitive dives may
explain why beaked whales appear to be particularly vulnerable to sonar
exposures. Further investigation is needed to further assess the
potential validity of these hypotheses. More information regarding
hypotheses that attempt to explain how behavioral responses to MFAS can
lead to strandings is included in the Behaviorally Mediated Bubble
Growth section, after the summary of strandings.
Acoustic Masking
Marine mammals use acoustic signals for a variety of purposes,
which differ among species, but include communication between
individuals, navigation, foraging, reproduction, and learning about
their environment (Erbe and Farmer, 2000; Tyack, 2000). Masking, or
auditory interference, generally occurs when sounds in the environment
are louder than and of a similar frequency to, auditory signals an
animal is trying to receive. Masking is a phenomenon that affects
animals that
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are trying to receive acoustic information about their environment,
including sounds from other members of their species, predators, prey,
and sounds that allow them to orient in their environment. Masking
these acoustic signals can disturb the behavior of individual animals,
groups of animals, or entire populations.
The extent of the masking interference depends on the spectral,
temporal, and spatial relationships between the signals an animal is
trying to receive and the masking noise, in addition to other factors.
In humans, significant masking of tonal signals occurs as a result of
exposure to noise in a narrow band of similar frequencies. As the sound
level increases, though, the detection of frequencies above those of
the masking stimulus decreases also. This principle is expected to
apply to marine mammals as well because of common biomechanical
cochlear properties across taxa.
Richardson et al. (1995) argued that the maximum radius of
influence of an industrial noise (including broadband low frequency
sound transmission) on a marine mammal is the distance from the source
to the point at which the noise can barely be heard. This range is
determined by either the hearing sensitivity of the animal or the
background noise level present. Industrial masking is most likely to
affect some species' ability to detect communication calls and natural
sounds (i.e., surf noise, prey noise, etc.; Richardson et al., 1995).
The echolocation calls of odontocetes (toothed whales) are subject
to masking by high frequency sound. Human data indicate low frequency
sound can mask high frequency sounds (i.e., upward masking). Studies on
captive odontocetes by Au et al. (1974, 1985, 1993) indicate that some
species may use various processes to reduce masking effects (e.g.,
adjustments in echolocation call intensity or frequency as a function
of background noise conditions). There is also evidence that the
directional hearing abilities of odontocetes are useful in reducing
masking at the high frequencies these cetaceans use to echolocate, but
not at the low-to moderate frequencies they use to communicate
(Zaitseva et al., 1980).
As mentioned previously, the functional hearing ranges of marine
mammals all encompass the frequencies of the active acoustic sources
used in the Navy's Keyport Range activities. Additionally, almost all
species' vocal repertoires span across the frequencies of the sources
used by the Navy. The closer the characteristics of the masking signal
to the signal of interest, the more likely masking is to occur.
However, because the pulse length and duty cycle of source signals are
of short duration and would not be continuous, masking is unlikely to
occur as a result of exposure to active acoustic sources during the
RDT&E activities in the Keyport Range Complex Extension Study Area.
Impaired Communication
In addition to making it more difficult for animals to perceive
acoustic cues in their environment, anthropogenic sound presents
separate challenges for animals that are vocalizing. When they
vocalize, animals are aware of environmental conditions that affect the
``active space'' of their vocalizations, which is the maximum area
within which their vocalizations can be detected before it drops to the
level of ambient noise (Brenowitz, 2004; Brumm et al., 2004; Lohr et
al., 2003). Animals are also aware of environmental conditions that
affect whether listeners can discriminate and recognize their
vocalizations from other sounds, which are more important than
detecting a vocalization (Brenowitz, 1982; Brumm et al., 2004; Dooling,
2004; Marten and Marler, 1977; Patricelli et al., 2006). Most animals
that vocalize have evolved an ability to make adjustments to their
vocalizations to increase the signal-to-noise ratio, active space, and
recognizability of their vocalizations in the face of temporary changes
in background noise (Brumm et al., 2004; Patricelli et al., 2006).
Vocalizing animals will make one or more of the following adjustments
to their vocalizations: Adjust the frequency structure; adjust the
amplitude; adjust temporal structure; or adjust temporal delivery.
Many animals will combine several of these strategies to compensate
for high levels of background noise. Anthropogenic sounds that reduce
the signal-to-noise ratio of animal vocalizations, increase the masked
auditory thresholds of animals listening for such vocalizations, or
reduce the active space of an animal's vocalizations impair
communication between animals. Most animals that vocalize have evolved
strategies to compensate for the effects of short-term or temporary
increases in background or ambient noise on their songs or calls.
Although the fitness consequences of these vocal adjustments remain
unknown, like most other trade-offs animals must make, some of these
strategies probably come at a cost (Patricelli et al., 2006). For
example, vocalizing more loudly in noisy environments may have
energetic costs that decrease the net benefits of vocal adjustment and
alter a bird's energy budget (Brumm, 2004; Wood and Yezerinac, 2006).
Shifting songs and calls to higher frequencies may also impose
energetic costs (Lambrechts, 1996).
Stress Responses
Classic stress responses begin when an animal's central nervous
system perceives a potential threat to its homeostasis. That perception
triggers stress responses regardless of whether a stimulus actually
threatens the animal; the mere perception of a threat is sufficient to
trigger a stress response (Moberg, 2000; Sapolsky et al., 2005; Seyle,
1950). Once an animal's central nervous system perceives a threat, it
mounts a biological response or defense that consists of a combination
of the four general biological defense responses: Behavioral responses,
autonomic nervous system responses, neuroendocrine responses, or immune
response.
In the case of many stressors, an animal's first and most
economical (in terms of biotic costs) response is behavioral avoidance
of the potential stressor or avoidance of continued exposure to a
stressor. An animal's second line of defense to stressors involves the
autonomic nervous system and the classical ``fight or flight'' response
which includes the cardiovascular system, the gastrointestinal system,
the exocrine glands, and the adrenal medulla to produce changes in
heart rate, blood pressure, and gastrointestinal activity that humans
commonly associate with ``stress.'' These responses have a relatively
short duration and may or may not have significant long-term effects on
an animal's welfare.
An animal's third line of defense to stressors involves its
neuroendocrine or sympathetic nervous systems; the system that has
received the most study has been the hypothalmus-pituitary-adrenal
system (also known as the HPA axis in mammals or the hypothalamus-
pituitary-interrenal axis in fish and some reptiles). Unlike stress
responses associated with the autonomic nervous system, virtually all
neuro-endocrine functions that are affected by stress--including immune
competence, reproduction, metabolism, and behavior--are regulated by
pituitary hormones. Stress-induced changes in the secretion of
pituitary hormones have been implicated in failed reproduction (Moberg,
1987; Rivier, 1995) and altered metabolism (Elasser et al., 2000),
reduced immune competence (Blecha, 2000) and behavioral disturbance.
Increases in the circulation of glucocorticosteroids (cortisol,
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corticosterone, and aldosterone in marine mammals; Romano et al., 2004)
have been equated with stress for many years.
The primary distinction between stress (which is adaptive and does
not normally place an animal at risk) and distress is the biotic cost
of the response. During a stress response, an animal uses glycogen
stores that can be quickly replenished once the stress is alleviated.
In such circumstances, the cost of the stress response would not pose a
risk to the animal's welfare. However, when an animal does not have
sufficient energy reserves to satisfy the energetic costs of a stress
respon