Endangered and Threatened Species: 12-Month Finding for a Petition to Revise Critical Habitat for Hawaiian Monk Seal, 27988-27994 [E9-13880]
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Federal Register / Vol. 74, No. 112 / Friday, June 12, 2009 / Proposed Rules
proposed rules.5 The RFA generally
defines the term ‘‘small entity’’ as
encompassing the terms ‘‘small
business,’’ ‘‘small organization,’’ and
‘‘small governmental entity.’’ 6 In
addition, the term ‘‘small business’’ has
the same meaning as the term ‘‘small
business concern’’ under the Small
Business Act.7 A small business concern
is one which: (1) Is independently
owned and operated; (2) is not
dominant in its field of operation; and
(3) satisfies any additional criteria
established by the Small Business
Administration (‘‘SBA’’).8 The proposed
rules and policies potentially will apply
to all FM radio broadcasting licensees
and potential licensees.
7. The SBA defines a radio
broadcasting station that has $7 million
or less in annual receipts as a small
business.9 A radio broadcasting station
is an establishment primarily engaged in
broadcasting aural programs by radio to
the public.10 Included in this industry
are commercial, religious, educational,
and other radio stations.11 Radio
broadcasting stations which primarily
are engaged in radio broadcasting and
which produce radio program materials
are similarly included.12 However, radio
stations that are separate establishments
and are primarily engaged in producing
radio program material are classified
under a separate NAICS number.13
According to Commission staff review
of the BIA Financial Network, Inc.
Media Access Radio Analyzer Database
as of February 19, 2009, about 10,600
(96 percent) of 11,050 commercial radio
stations in the United States have
revenues of $7 million or less. We note
that many radio stations are affiliated
with much larger corporations having
much higher revenue. Our estimate,
therefore, likely overstates the number
of small entities that might be affected
by our action.
55
U.S.C. 603(b)(3).
U.S.C. 601(6).
7 5 U.S.C. 601(3) (incorporating by reference the
definition of ‘‘small business concern’’ in the Small
Business Act, 15 U.S.C. 632). Pursuant to 5 U.S.C.
601(3), the statutory definition of a small business
applies ‘‘unless an agency, after consultation with
the Office of Advocacy of the Small Business
Administration and after opportunity for public
comment, establishes one or more definitions of
such term which are appropriate to the activities of
the agency and publishes such definition(s) in the
Federal Register.’’
8 15 U.S.C. 632.
9 See 13 CFR 121.201, NAICS Code 515112
(changed from 513112 in October 2002).
10 Id.
11 Id.
12 Id.
13 Id.
65
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D. Description of Projected Reporting,
Recordkeeping and Other Compliance
Requirements
8. In the Second Report and Order,
the Commission declined to establish a
deadline for radio stations to convert to
digital broadcasting, 22 FCC Rcd at
10351. Presently, radio stations may
choose to commence DAB operation
pursuant to Section 73.404 of the
Commission’s rules, 47 CFR 73.404,
which requires in part that licensees
provide notification to the Commission
within 10 days of commencing DAB
operation. The proposed rule change
may impose additional reporting or
recordkeeping requirements on FM
radio stations choosing to upgrade DAB
operating power above the current
limitation of 1 percent of a station’s
authorized analog power. For example,
licensees choosing to increase DAB
operating power above 1 percent of
authorized analog power could be
required to notify the Commission of the
increase in power.
E. Steps Taken To Minimize Significant
Impact on Small Entities, and
Significant Alternatives Considered
9. The RFA requires an agency to
describe any significant alternatives that
it has considered in reaching its
proposed approach, which may include
the following four alternatives (among
others): (1) The establishment of
differing compliance or reporting
requirements or timetables that take into
account the resources available to small
entities; (2) the clarification,
consolidation, or simplification of
compliance or reporting requirements
under the rule for small entities; (3) the
use of performance, rather than design,
standards; and (4) an exemption from
coverage of the rule, or any part thereof,
for small entities.14 This document has
proposed for commenter evaluation the
issue of taking steps to minimize
significant impact on small entities,
focusing on the four issues, enumerated
supra in paragraph 6, relevant to the
Joint Parties’ Request, as well as on any
issues raised by the technical studies
previously submitted by iBiquity and
NPR. To assist in the analysis,
commenters are requested to provide
information, studies, and/or opinions
regarding how small entities would be
affected if the Commission were to
adopt an increase in maximum digital
operating power as proposed by the
Joint Parties or a provisional power
increase of some lesser extent than that
requested by the Joint Parties, and
whether such adoption could result in
14 5
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U.S.C. 603(b).
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the disparate treatment of small entities
with limited financial and/or technical
resources. Commenters should also
provide information, studies, and/or
opinions on alternative approaches to
alleviate any potential burdens on small
entities.
F. Federal Rules Which Duplicate,
Overlap, or Conflict With, the
Commission’s Proposals
10. None.
Federal Communications Commission.
Robert H. Ratcliffe,
Acting Chief, Media Bureau.
[FR Doc. E9–13865 Filed 6–11–09; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
50 CFR Part 226
[Docket No. 0809161218–9950–02]
RIN 0648–AX23
Endangered and Threatened Species:
12–Month Finding for a Petition to
Revise Critical Habitat for Hawaiian
Monk Seal
AGENCY: National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice of 12–month finding.
SUMMARY: On July 9, 2008, we (NMFS)
received a petition dated July 2, 2008,
requesting that we revise the present
critical habitat designation for the
Hawaiian monk seal (Monachus
schauinslandi) under the Endangered
Species Act (ESA) by expanding the
current critical habitat in the
Northwestern Hawaiian Islands, and by
designating additional critical habitat in
the main Hawaiian Islands. We have
reviewed, and here provide a summary
of the best available information
regarding Hawaiian monk seal biology
and habitat use. Based on our review,
we intend to revise the monk seal’s
critical habitat, and we are providing
our initial thoughts on the habitat
features that are essential to the
conservation of this species and
describing how we intend to proceed
with the requested critical habitat
revision.
ADDRESSES: Requests for copies of this
determination should be addressed to
the Assistant Regional Administrator,
Protected Resources Division, NMFS,
1601 Kapiolani Blvd, Honolulu, HI
96814.
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Federal Register / Vol. 74, No. 112 / Friday, June 12, 2009 / Proposed Rules
FOR FURTHER INFORMATION CONTACT:
Lance Smith at (808) 944–2258, e-mail
lance.smith@noaa.gov; Krista Graham at
(808) 944–2238, e-mail
krista.graham@noaa.gov; or Marta
Nammack, (301) 713–1401.
SUPPLEMENTARY INFORMATION:
Background documents on the biology
of the Hawaiian monk seal, the July 2,
2008, petition requesting revision of its
critical habitat, and documents
explaining the critical habitat
designation process, can be downloaded
from https://www.fpir.noaa.gov/PRD/
prdlindex.html, or requested by phone
or e-mail from the NMFS staff in
Honolulu (area code 808) listed under
‘‘FOR FURTHER INFORMATION CONTACT’’.
The October 3, 2008, 90–day finding in
response to the petition and the
information received in response to the
90–day finding can be viewed at
www.regulations.gov by searching for
docket number ‘‘NOAA-NMFS–2008–
0290’’.
Background
On July 9, 2008, we received a
petition dated July 2, 2008, from the
Center for Biological Diversity, Kahea,
and the Ocean Conservancy (Petitioners)
to revise the Hawaiian monk seal
critical habitat designation (Center for
Biological Diversity et al., 2008) under
the ESA. Currently designated critical
habitat is described below in ‘‘Listing
Status and Existing Critical Habitat
Under the ESA.’’ The Petitioners seek to
revise critical habitat by adding the
following areas in the main Hawaiian
Islands (MHI): key beach areas, sand
spits and islets, including all beach crest
vegetation to its deepest extent inland,
lagoon waters, inner reef waters, and
ocean waters out to a depth of 200
meters. In addition, The Petitioners
request that currently designated critical
habitat in the Northwestern Hawaiian
Islands (NWHI) be extended to include
Sand Island at Midway, as well as ocean
waters out to a depth of 500 meters
(Center for Biological Diversity et al.,
2008).
On October 3, 2008, we published a
90–day finding in response to the
petition, finding that the petition
presented substantial scientific
information indicating that a revision to
the current critical habitat designation
may be warranted (73 FR 57583;
October 3, 2008). The 90–day finding
requested that the public submit
information by December 2, 2008, to
help us determine whether a revision of
critical habitat is warranted for the
Hawaiian monk seal. The purpose of
this 12–month finding is to announce
that we intend to proceed with a
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revision of critical habitat for the monk
seal and to provide details on the
revision process.
In the following sections, we provide
information on the Hawaiian monk
seal’s listing status and existing critical
habitat under the ESA, population
status and trend, Hawaiian monk seal
biology, summary of the information
received from the public in response to
our 90–day finding (73 FR 57583;
October 3, 2008), our determination that
we will proceed with a revision of
critical habitat, and the criteria we
intend to use for the revision.
Listing Status and Existing Critical
Habitat Under the ESA
The Hawaiian monk seal (Monachus
schauinslandi) was listed as endangered
under the ESA in 1976 (41 FR 33922;
November 23, 1976). This species
occurs throughout the Hawaiian
Archipelago and on Johnston Atoll, and
has been sighted at other atolls and
islands to the south of Hawaii. In 1986,
critical habitat was designated for all
beach areas, sand spits and islets,
including all beach crest vegetation to
its deepest extent inland, lagoon waters,
inner reef waters, and ocean waters out
to a depth of 10 fathoms (18.3 m)
around Kure Atoll, Midway Islands
(except Sand Island), Pearl & Hermes
Reef, Lisianski Island, Laysan Island,
Gardner Pinnacles, French Frigate
Shoals, Necker Island, and Nihoa Island
in the NWHI (51 FR 16047; April 30,
1986). In 1988, critical habitat was
extended to include Maro Reef and
waters around previously recommended
areas out to the 20 fathom (36.6 m)
isobath (53 FR 18988; May 26, 1988). A
recovery plan was completed in 1983
(NMFS, 1983) and revised in 2007
(NMFS, 2007a). The species is endemic
(found nowhere else) to the Hawaiian
Archipelago, and is one of the most
endangered marine mammals in the
United States (NMFS, 2007a).
Hawaiian Monk Seal Biology
The Hawaiian monk seal is a mammal
in the Order Carnivora, Family
Phocidae, Genus Monachus. Only two
other species occur in this genus, the
recently extinct Caribbean monk seal
(M. tropicalis) and the critically
endangered Mediterranean monk seal
(M. monachus). Following is an
overview of the Hawaiian monk seal’s
biology, including Range, Population
Status and Trends, Natural History,
Habitat, and Northwestern Hawaiian
Islands vs. Main Hawaiian Islands (a
description of differences in monk seal
habitat between these two areas).
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Range
Hawaiian monk seals are found
throughout the Hawaiian Archipelago
and on Johnston Atoll. The six main
reproductive sites for the species are in
the NWHI: Kure Atoll, Midway Islands,
Pearl and Hermes Reef, Lisianski Island,
Laysan Island, and French Frigate
Shoals. Smaller reproductive sites also
occur on Necker Island and Nihoa
Island, and monk seals have been
observed at Gardner Pinnacles and Maro
Reef. Monk seals are found throughout
the MHI, where births have been
documented on most of the major
islands (NMFS, 2001, 2007a). In 1994,
we relocated 21 adult male monk seals
from the NWHI to the MHI in order to
reduce male aggression and female
deaths at Laysan Island, where males
greatly outnumbered females at the
time. We have relocated three female
monk seals (a juvenile in 1981, a pup in
1991, and an adult in 2009) from the
MHI to the NWHI. Thus, we have
relocated 21 males from the NWHI to
the MHI, and three females from the
MHI to the NWHI.
At Johnston Atoll, a tagged yearling
male monk seal from Laysan Island was
first seen in July 1968 (Schreiber and
Kilder, 1969) and remained until at least
August 1972. In January 1969, an
untagged adult female monk seal arrived
on Sand Island, a secondary island
within Johnston Atoll, and gave birth to
a female pup. The mother-pup pair
remained on or near the pupping beach
until March 1969, when the pup was
weaned and the mother disappeared.
The pup remained until 1971 when it
died from a deep flesh wound, probably
from a shark attack (Amerson and
Shelton, 1976). In July 1999, a tagged
adult female from French Frigate Shoals
arrived at Johnston Atoll and remained
there for about a year (NMFS, 2001).
In addition to the above reported
natural occurrences of monk seals at
Johnston Atoll, a 12 male monk seals
have been relocated there from the
Hawaiian Archipelago. In 1984, nine
adult males were relocated from the
NWHI to Johnston Atoll, because of
attacks on adult females and immature
seals. At least three of these males were
still at Johnston Atoll the following
year, and at least one male was still
there in 1986. In 1989, two adult males
were relocated from the NWHI to
Johnston Atoll because they were
drowning pups. In 2003, an adult male
was relocated from the MHI to Johnston
Atoll because it was habituated to
humans and exhibiting dangerous
behavior. No sighting history is
available for the latter three monk seals
(NMFS unpublished data).
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Federal Register / Vol. 74, No. 112 / Friday, June 12, 2009 / Proposed Rules
Unconfirmed but probable sightings
of Hawaiian monk seals outside the
Hawaiian Archipelago and Johnston
Atoll have been reported from Palmyra
Atoll (1,800 km south of NWHI) and
Wake Island (2,000 km southwest of
NWHI); two seals were sighted on
Palmyra Atoll in 1990, a seal was
sighted on Wake Island in early summer
1966, and a tagged seal was sighted on
Wake Island in February 1987 (Westlake
and Gilmartin, 1990, NMFS
unpublished data). Other more poorlydocumented sightings have also been
reported from Bikini Atoll and Mejit
Island in the Marshall Islands (2,400 km
southwest of NWHI, NMFS unpublished
data).
Population Status and Trends
The best estimate of Hawaiian monk
seal total population size is 1,208 seals
in 2006 (1,125 in the NWHI, 83 in the
MHI; NMFS, 2008a). Additional
population information can be found in
the annual Stock Assessment Reports
(e.g., NMFS, 2006, 2007b, 2008a). The
first rangewide beach count surveys of
Hawaiian monk seals were conducted in
the late 1950s. Beach counts of juveniles
and adults (i.e., all seals except pups)
declined by 66 percent between the
years 1958 and 2006 (Figure I.C.6 in
NMFS, 2007a). More recently, beach
counts declined rapidly from 1985 to
1993, and then became relatively stable
until the current decline began in 2001.
Total abundance at the six primary
NWHI sites (French Frigate Shoals,
Laysan, Lisianski, Pearl and Hermes,
Midway, and Kure) is declining at a rate
of about four percent per year (NMFS
2007a, 2007b, 2008a).
Since 2000, many sites have shown
indications of decline in abundance,
apparently due to low juvenile survival.
The decline at French Frigate Shoals is
of particular consequence to the welfare
of the overall population because this
site once accounted for over 50 percent
of the total non-pup beach counts in the
NWHI. While that proportion has now
dropped to approximately 25 percent of
its observed peak, there are still more
seals at French Frigate Shoals than any
other island or atoll. More detail on
Hawaiian monk seal population status
and trends in the NWHI is provided in
the recovery plan (NMFS, 2007a). As
noted above, in 1994, we relocated 21
adult male monk seals from the NWHI
to the MHI in order to reduce male
aggression and female deaths at Laysan
Island, where males greatly
outnumbered females at the time. All
female monk seals in the MHI occur
there naturally. In 2008, only five of the
21 relocated male monk seals remained
in the MHI.
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Although monk seals historically
occurred throughout the Hawaiian
Archipelago, the majority of the
population now occurs in the NWHI.
Human settlement appears to have
largely excluded monk seals from the
MHI, although seal bones have been
found at archeological sites dating from
1400 - 1700 (Rosendahl, 1994). In 1900,
Hilo residents reported that solitary
monk seals were seen in the area about
once every 10 years (Bailey, 1952). From
1928 to 1956, seven monk seal sightings
were documented in the MHI (Kenyon
and Rice, 1959), and Niihau residents
reported that seals appeared there in the
1970s. By 1994 there was a small
naturally-occurring population of male
and female monk seals in the MHI. This
population appeared to be growing, and
at least six pups had been born (one in
1962, and five between 1988 and 1993).
Since the mid–1990s, an increasing
number of documented sightings and
annual births of monk seal pups have
occurred in the MHI. Combined aerial
and ground surveys in the MHI counted
45 hauled-out monk seals in 2000, and
52 in 2001 (Baker and Johanos, 2004).
Sightings in the MHI tallied 77
individually identifiable monk seals in
2005 (NMFS, 2007b), and 83 in 2006
(NMFS, 2008a). Together, these
observations suggest that monk seals are
recolonizing the MHI.
Natural History
Hawaiian monk seals are wideranging, air-breathing predators that
forage underwater, preying primarily on
small benthic fishes, cephalopods (e.g.,
octopus), and crustaceans (GoodmanLowe, 1998). They spend the majority of
their time in the ocean, where they are
highly mobile and may have very large
home ranges (Antonelis et al., 2006).
Monk seals are typical large predators,
in that they can rapidly cover large areas
in search of food. Individuals may travel
hundreds of miles in a few days (Littnan
et al., 2007) and dive to 500 m (1,600
ft; Parrish et al., 2002). Monk seals haul
out on land to rest, molt, pup (give
birth), and nurse. Resting may also
occur at sea or in shallow, submerged
caves. Monk seals are often solitary,
both on land and in the water, but may
congregate in favorable haul-out areas
(Antonelis et al., 2006). Adult monk
seals reach a length of 2.3 m (7.5 ft) and
weigh up to 273 kg (600 lb). Unlike most
other pinnipeds, monk seals completely
molt, whereby the entire layer of pelage
(skin and hair) is shed annually. The old
pelage strips away, leaving a dark grey
coat underneath. Pups are black until
first molt, and mostly grey thereafter,
although coloration varies by individual
and with age. When monk seals stay at
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sea for an extensive period, they may
develop a red or green tinge from algal
growth on their pelage (Kenyon and
Rice, 1959).
It is thought that Hawaiian monk seals
have a lifespan of up to 30 years.
Females reach breeding age at about 6
to 11 years of age, depending on their
condition, and give birth no more than
once annually. Mating occurs at sea, and
gestation is thought to be approximately
11 months. Monk seal births are most
common between February and August,
peaking in March and April at Laysan
Island. Females give birth to a single
pup and nurse it for about 6 weeks,
followed by an abrupt weaning, when
the mother abandons the pup (Johanos
et al., 1994). At least several months are
required for the pup to learn to forage
successfully on its own, during which
time it survives on fat stores built up
during nursing, resulting in
considerable weight loss. Juveniles (up
to 3 years old) are typically longer but
thinner than recently-weaned pups, and
juveniles in the NWHI typically do not
regain their weaning weight until
approximately 2 years of age (Johanos et
al., 1994). Male aggression, in which a
single male or multiple males
repeatedly attempt to mount and mate
with a female or immature seal, is most
common where males outnumber
females, and sometimes results in death
or severe injury to the targeted seal.
Individual adult males sometimes attack
pups in the same manner, also
sometimes killing the pup (Hiruki et al.,
1993).
Habitat
While Hawaiian monk seals spend
most of their time in the water, they
frequently haul out on land to rest, molt,
pup (give birth), and nurse. Monk seals
may remain at sea for several days or
more at a time, but resting on land is
necessary to conserve energy. Resting is
commonly on sandy beaches, but may
also occur on rocky shores, rock ledges,
emergent reefs, and even shipwrecks
(Antonelis et al., 2006). Monk seals may
take shelter from wind and rain under
shoreline vegetation. Resting on land is
typically done for a few hours to several
days at a time, after which the monk
seal returns to the water to continue
foraging. When ocean conditions are
rough, monk seals may spend a greater
proportion of time resting on land.
Hauling-out on land is also required for
molting, when old pelage is shed.
Molting is an annual process taking 1 to
2 weeks, during which time the monk
seal usually remains on land (Kenyon
and Rice, 1959).
Pupping and nursing areas are usually
sandy beaches adjacent to shallow
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protected water (Westlake and
Gilmartin, 1990). Individual females
appear to favor certain pupping
locations, returning to them year after
year. Pregnant females come ashore a
few days before giving birth to a pup
weighing approximately 16 kg (35 lb).
Pups nurse for 5 to 6 weeks (Johanos et
al., 1994), and weigh 50 - 100 kg (110
- 220 lb) at weaning. During nursing, the
mother-pup pair remain close to each
other, and the mother is protective of
her pup. Although the pup is able to
swim at birth, nursing is done on land,
and the mother-pup pair usually remain
on land for the first few days after the
pup is born. The mother gradually
begins swimming with her pup in the
shallows, returning to the general area
around the pupping site. As weaning
approaches, the mother-pup pair spend
more time in the water, venturing
further away from the pupping site.
After weaning, pups typically remain in
the shallows near their nursing areas for
several weeks before venturing into
deeper foraging areas (Kenyon and Rice,
1959; Henderson and Johanos, 1988).
Monk seals are generalists that forage
primarily over low-relief substrates such
as sand and talus. Live fish are generally
the preferred prey, and over 150 fish
species have been recorded in the monk
seal diet (Iverson et al., 2006). NWHI
camera studies have shown that adult
male monk seals forage mainly on sand
terraces and talus slopes 50 - 100 m (160
- 325 ft) deep around their home atoll
and nearby seamounts (Parrish and
Littnan, 2008). Premium adult foraging
habitat is comprised of large, loose talus
fragments, which the seals move to
reach the hiding prey underneath
(Parrish et al., 2000). Studies in the
NWHI (Parrish et al., 2002; Stewart et
al., 2006) have shown that adult monk
seals may forage at 300 - 500 m (1,000
- 1,600 ft), sometimes visiting patches of
deep corals (Parrish et al., 2002). Recent
surveys of deep fish assemblages across
seamounts of the NWHI show a pattern
of reduced fish biomass at sites close to
colonies of monk seals (Parrish, 2009).
Juvenile monk seals (1 - 3 years old)
forage both within shallow atoll lagoons
10 - 30 m (30 - 100 ft) and on deep reef
slopes (50 - 100 m/160 - 325 ft), usually
over sand rather than talus. Juvenile
seals likely do not yet have the size or
experience to engage in the large talusforaging behavior exhibited by adults
(Parrish et al., 2005).
Although much less information is
available for monk seals in the MHI, 11
juvenile and adult monk seals were
tracked there in 2005 using satellitelinked radio transmitters showing
location but not depth. This study
indicated that seals usually remained in
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Johanos, 2004; Baker et al., 2006).
Although the NWHI is one of the largest
and best-protected natural areas in the
world, and the MHI are populated by
over a million people, the latter appears
to currently provide superior monk seal
foraging conditions.
Despite its large human population,
the MHI may currently provide better
monk seal foraging conditions than the
NWHI because: (1) There are only about
one-tenth the number of seals in the
MHI than in the NWHI, thus the
availability of prey may be higher per
seal in the MHI than the NWHI (Baker
and Johanos, 2004); and (2) Large
sharks, jacks and other demersal fish
compete directly with monk seals, but
are much less abundant in the MHI than
the NWHI (Parrish et al., 2008).
Competition is limited between humans
and monk seals in the MHI because
seals prefer small (usually < 20 cm/8 in)
eels, wrasses, and other benthic species
not commonly sought by fishermen,
(Parrish et al., 2000). However, while
foraging conditions are currently better
in the MHI than the NWHI for monk
seals, pollution and runoff pose health
hazards to the species in the MHI not
found in the NWHI (Littnan et al., 2007).
As described above in Population
Status and Trends, since 1990, the total
number of Hawaiian monk seals has
decreased, while simultaneously the
number of monk seals in the MHI
appear to have increased (NMFS, 2006,
2007b, 2008a). As described in the
above paragraph, foraging conditions
currently appear better in the MHI than
in the NWHI (Parrish et el., 2000, 2008),
likely resulting in better physical
condition and higher survival of seals in
the MHI than in the NWHI (Baker and
Johanos; 2004; NMFS, 2007a). In
addition, sea level rise may reduce or
Northwestern Hawaiian Islands vs. Main eliminate monk seal haul-out habitat
Hawaiian Islands
more rapidly in the low-lying NWHI
The Hawaiian monk seal consists of
than the MHI (Baker et al., 2006). Given
one population distributed throughout
the overall downward trend of the
the Hawaiian Archipelago. That is, there species (see Population Status and
is no evidence that monk seals
Trends above), generally poor physical
occurring in any part of the archipelago
condition and survival of seals in the
are genetically distinct from those
NWHI, and proportionally greater sea
elsewhere in the archipelago (Schultz et level effects on the NWHI than the MHI,
al., 2008). This suggests that the
the MHI appears essential for the
population is genetically well-mixed,
survival and recovery of this species.
with individual seals sometimes moving
between the NWHI and the MHI, which Summary of Information Received
In our 90–day finding (73 FR 5l7583;
has been confirmed with resightings of
October 3, 2008) in response to the
flipper-tagged or otherwise identifiable
petition (Center for Biological Diversity
(e.g., scar patterns; Littnan et al., 2007).
et al., 2008), we solicited information
However, monk seals in the MHI are
from the public pertaining to the
typically in better physical condition
Hawaiian monk seal’s essential habitat
than those in the NWHI. For example,
needs. The 90–day finding, and the
weaned pups in the MHI are larger and
information we received in response to
fatter than those in the NWHI, which is
it, can be viewed at
thought to reflect better foraging
www.regulations.gov by searching for
conditions in the MHI (Baker and
nearshore waters within the 200 m (650
ft) isobath. As in the NWHI, this study
suggested that monk seals in the MHI
forage mainly in deeper, low-relief
(talus, sand) areas, commuting over
shallower, high-relief (coral reefs, rock
outcrops) without foraging (Littnan et
al., 2007). However, as in the NWHI,
shallow areas adjacent to pupping areas
are important for pups to develop
foraging behavior. Otherwise, coral reefs
and other high-relief shallows are not
usually primary monk seal foraging
habitat. Generally, juvenile and adult
monk seals bypass these shallow highrelief substrates in transit to their
primary foraging areas over low-relief
substrates in deeper water, sometimes
making no attempt to hunt the same fish
species in the shallows that they were
actively hunting in the deep (Parrish
and Littnan, 2008).
In summary, the physical and
biological habitat features that support
resting, reproduction, and foraging are
essential for the conservation of this
species. For the Hawaiian monk seal,
essential habitat includes terrestrial and
marine areas. Terrestrial areas include
both resting and reproductive habitat.
Resting habitat consists of nearshore or
emergent surfaces where monk seals can
haul out, whereas reproductive habitat
consists of a subset of resting habitat on
sandy beaches that are also suitable for
pupping and nursing. Marine areas
include foraging habitat for pups,
juveniles, and adults. Pup foraging
habitat consists of shallow areas
adjacent to pupping beaches where
pups become accustomed to the marine
environment and begin learning to
forage on their own. Juveniles and
adults forage widely, primarily in
deeper areas.
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docket number ‘‘NOAA-NMFS–2008–
0290’’. The great majority of the monk
seal habitat-related information received
was based on programs and studies
conducted, funded, or supported by
NMFS; therefore, we did not receive any
new information on the monk seal’s
essential habitat needs. The information
received is summarized below.
Comment 1: Over 100 comments
argued that the MHI provide essential
habitat for the Hawaiian monk seal
because: (1) the MHI component of the
monk seal population has increased in
recent years while simultaneously the
overall population has decreased; (2)
monk seals in the MHI are in better
physical condition than those in the
NWHI; and (3) monk seal habitat loss is
likely to be much more rapid in the
NWHI than in the MHI in the near
future due to sea level rise.
Response: We concur that the MHI
component of the monk seal population
appears to have increased in recent
years while simultaneously the overall
population has decreased (see
‘‘Population Size and Trends’’ above),
that monk seals in the MHI are in better
physical condition than those in the
NWHI, and that monk seal haul-out
habitat loss is likely to be more rapid in
the NWHI than in the MHI in the future
due to sea level rise (see ‘‘Northwestern
Hawaiian Islands vs. Main Hawaiian
Islands’’ above). For these three reasons,
and also because of the current
precarious state of the Hawaiian monk
seal, we agree that monk seal habitat
within the MHI is essential for the
survival and recovery of the species.
Comment 2: Several comments argued
that the MHI do not provide essential
habitat for the Hawaiian monk seal,
because: (1) monk seals are not
indigenous to the MHI; and (2) various
human threats to monk seals in the MHI
outweigh benefits to the species of MHI
habitat.
Response: Little evidence has been
found that monk seals occurred in the
MHI before the arrival of humans
approximately 2,000 years ago, or
during pre-European times before the
late 1700s. However, before the arrival
of humans, monk seal remains would
typically have occurred on or near
coastlines where wave action and
erosion likely would have prevented
preservation of remains. After the
arrival of humans, monk seals may have
been consumed by humans, in which
case monk seal bones would likely
occur in middens. However, if the seals
were quickly extirpated after the arrival
of humans, this would reduce the
likelihood of finding bone fragment
evidence in middens. An archeological
dig of a midden on the Big Island
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identified monk seal bones, and
estimated that the bones were deposited
during the years 1400 to 1700
(Rosendahl, 1994). Furthermore, monk
seals commonly travel long distances
between atolls or islands, and even
between the NWHI and MHI (Littnan et
al., 2007). Thus, before the arrival of
humans, it is highly unlikely that monk
seals occurred only in the NWHI, while
the MHI were vacant of both monk seals
and humans. Finally, large, easilyhunted animals such as seals are
typically extirpated or driven to
extinction when humans arrive in an
area for the first time (Grayson, 2001).
Arrival of humans in Hawaii likely
resulted in a rapid reduction in monk
seal numbers in the MHI, such that the
species was mostly restricted to the
NWHI until recently (Baker and
Johanos, 2004). For these reasons, we
believe that the Hawaiian monk seal
commonly occurred in the MHI before
the arrival of humans, and that this
species is indigenous to at least the
entire Hawaiian Archipelago.
We agree that the Hawaiian monk seal
faces a multitude of human threats in
the MHI. The recovery plan identifies
the most serious human threats to monk
seals in the MHI as infectious diseases,
fisheries interactions, habitat loss, and
human interactions (NMFS, 2007a). In
the MHI, monk seals forage near shore,
and they haul out on beaches near
sources of pathogens associated with
human population centers, sewage
spills, and stream mouths. Of 12 dead
monk seals that were thoroughly
necropsied in the MHI between 1996
and 2006, four appeared to have died of
infectious disease (Littnan et al., 2007).
In the MHI from 1989 to 2007, 44 monk
seals were confirmed to be hooked by
fishing gear (one of which died, possibly
from the hooking), another five
entangled in lay gillnets (three of which
drowned in the gillnets), and one seal
hooked and entangled (but survived).
Many hooks are removed from monk
seals by the monk seal response
program, most often resulting in healing
of the wound and recovery of the monk
seal. However, entanglement in lay
gillnets often results in the drowning of
the monk seal (NMFS, 2008b). Monk
seal haul-out beaches in the MHI are
being degraded or lost by development
adjacent to the beaches, and increasing
human activity on the beaches. The high
and ever-increasing human use of MHI
beaches and coastlines results in
humans frequently interacting with
monk seals, both unintentionally and
intentionally (NMFS, 2007a). However,
despite the numerous anthropogenic
threats to monk seals in the MHI, the
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MHI component of the monk seal
population appears to have increased in
recent years, and monk seals in the MHI
are generally in good physical
condition. In contrast, the NWHI
component of the monk seal population
continues to decrease, and monk seals
in the NWHI are often in poor physical
condition (see ‘‘Population Size and
Trends’’ and ‘‘Northwestern Hawaiian
Islands vs. Main Hawaiian Islands’’
above). Thus, although monk seals are
more often exposed to infectious
diseases in the MHI than in the NWHI,
the MHI appear to currently provide a
favorable environment for monk seals.
In addition, the loss of monk seal haulout habitat is likely to occur more
rapidly in the NWHI than the MHI due
to sea level rise (see ‘‘Northwestern
Hawaiian Islands vs. Main Hawaiian
Islands’’ above). For these reasons, we
believe that the benefits of MHI habitat
to the monk seal outweigh the various
human threats to monk seals in the
MHI.
Comment 3: Over 100 comments
argued that areas out to a depth of 500
m (1,625 ft) in the NWHI provide
essential foraging habitat for the
Hawaiian monk seal.
Response: As discussed above in
‘‘Habitat,’’ studies in the NWHI have
documented adult monk seal foraging to
a maximum depth of approximately 500
m (1,600 ft; Parrish et al., 2002; Stewart
et al., 2006). The relative importance of
these deep foraging areas, compared to
more frequently-used shallower areas, is
currently unknown.
Comment 4: Several comments did
not provide any information about
habitat use by the Hawaiian monk seal,
but rather expressed opinions about the
effects of revising monk seal critical
habitat on various human activities,
such as beach use, fishing, economics,
national security, and natural resource
management.
Response: The economic, national
security, and other effects of revising
monk seal critical habitat will be
addressed in the forthcoming proposed
rule.
12–Month Determination on Revision of
Critical Habitat
Since critical habitat for the Hawaiian
monk seal was designated in 1986 (51
FR 16047; April 30, 1986) and revised
in 1988 (53 FR 18988; May 26, 1988), a
great deal of new information has
become available regarding habitat use
by this species, such as the literature
cited in the petition (Center for
Biological Diversity et al., 2008) and in
the Recovery Plan (NMFS, 2007a). For
example, studies of monk seal foraging
made possible by new technology (e.g.,
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Parrish et al. 2000, 2002, 2005, 2008;
Littnan et al., 2007) have resulted in
substantial progress since 1988 in
understanding how this species uses
foraging habitat (Parrish and Littnan,
2008). Also, since critical habitat was
designated in 1988, monk seals appear
to have begun recolonizing the MHI
(Baker and Johanos, 2004; Baker et al.,
2006; NMFS, 2007a). Other information
has also become available about other
aspects of monk seal life history and
habitat use (summarized in NMFS,
2007a). Because of this new information
regarding habitat use by the Hawaiian
monk seal that has become available
since critical habitat for the species was
revised in 1988 (53 FR 18988; May 26,
1988), we will proceed with a revision
of critical habitat for the species.
How Does NMFS Intend To Proceed?
We intend to undertake rulemaking to
revise critical habitat for the Hawaiian
monk seal. Critical habitat is defined by
section 3 of the ESA as ‘‘(i) the specific
areas within the geographical area
occupied by the species, at the time it
is listed in accordance with the
provisions of section 1533 of this title,
on which are found those physical or
biological features (I) essential to the
conservation of the species and (II)
which may require special management
considerations or protection; and (ii)
specific areas outside the geographical
area occupied by the species at the time
it is listed in accordance with the
provisions of section 1533 of this title,
upon a determination by the Secretary
that such areas are essential for the
conservation of the species.’’ Further,
our critical habitat regulations (50 CFR
424.12(c)) state that critical habitat will
be defined by specific limits using
reference points and lines on standard
topographic maps of the area. Finally,
section 4(b)(2) of the ESA requires that
we consider economic, national
security, and other impacts of
designating critical habitat before
designating critical habitat.
Based on the above definition and
guidance, the following steps will be
followed to propose the revision of
designated critical habitat for the
Hawaiian monk seal: (1) Determine the
geographical area occupied by the
species at the time of listing; (2) Identify
the physical or biological features
essential to the conservation of the
species; (3) Delineate areas within the
geographical area occupied by the
species that contain these features, and
that may require special management
considerations or protections; (4)
Delineate any areas outside of the
geographical area occupied by the
species that are essential for the
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Jkt 217001
conservation of the species; and (5)
Conduct economic, national security,
and other analyses to determine if any
areas identified in steps 3 and 4 could
be excluded from critical habitat
consideration under section 4(b)(2) of
the ESA. Steps 1 and 2 above are
included in this 12–month finding, as
described below. Steps 3 - 5 will be
completed in the forthcoming proposed
rule.
Step 1: Determine Geographical Area
Occupied by the Species at the Time of
Listing: The final rule listing the
Hawaiian monk seal as endangered,
published on November 23, 1976 (41 FR
51611), stated that the ‘‘Hawaiian monk
seal is found throughout the Hawaiian
Archipelago,’’ with no mention of areas
outside the archipelago. For reasons
described above in ‘‘Range,’’ in 2001,
we determined that Johnston Atoll is
within the range of the Hawaiian monk
seal (NMFS, 2001). Therefore, the
geographical area occupied by the
Hawaiian monk seal at the time of
listing (1976) is considered to be the
Hawaiian Archipelago and Johnston
Atoll.
Step 2: Identify Physical or Biological
Features Essential to Conservation: In
this step, the physical and biological
features essential to conservation are
identified (hereafter referred to as
‘‘essential features’’). Section 3 of the
ESA (16 U.S.C. 1532(3)) defines the
terms ‘‘conserve,’’ ‘‘conserving,’’ and
‘‘conservation’’ to mean: ‘‘to use, and
the use of, all methods and procedures
which are necessary to bring any
endangered species or threatened
species to the point at which the
measures provided pursuant to this
chapter are no longer necessary.’’ Our
critical habitat regulations (50 CFR
424.12(b)) state that essential features
‘‘include, but are not limited to the
following: (1) Space for individual and
population growth, and for normal
behavior; (2) Food, water, air, light,
minerals or other nutritional or
physiological requirements; (3) Cover or
shelter; (4) Sites for breeding,
reproduction, rearing of offspring,
germination, or seed dispersal; and
generally; (5) Habitats that are protected
from disturbance or are representative of
the historic geographical and ecological
distributions of a species.’’
The regulations also instruct us to
‘‘focus on the principal biological or
physical constituent elements within
the defined area that are essential to the
conservation of the species. Known
primary constituent elements shall be
listed with the critical habitat
description’’ (50 CFR 424.12(b)). Thus,
the essential features will be defined
here in terms of primary constituent
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27993
elements (PCEs). The PCEs can include
sites used by the listed species for
resting, reproduction, and feeding
(examples given in the regulations
include ‘‘nesting grounds, spawning
sites, feeding sites’’), and physical
features of the species’ habitat
(examples given in the regulations
include ‘‘geological formation,
vegetation type, tide, and specific soil
types’’; 50 CFR 424.12(b)).
As described above in ‘‘Habitat,’’ the
physical and biological habitat features
that support resting, molting,
reproduction, and foraging are essential
for the conservation of this species. For
the Hawaiian monk seal, essential
habitat includes terrestrial and marine
areas. Terrestrial areas include resting,
molting, and reproductive habitat.
Resting and molting habitat consists of
nearshore or emergent surfaces where
monk seals can haul out, whereas
reproductive habitat consists of a subset
of resting and molting habitat (i.e.,
sandy beaches suitable for pupping and
nursing). Marine areas include foraging
habitat for pups, juveniles, and adults.
Pup foraging habitat consists of shallow
areas adjacent to pupping beaches
where pups become accustomed to the
marine environment and begin learning
to forage on their own. Juveniles and
adults forage widely, primarily in
deeper areas. Thus, at this time, we
believe that the following PCEs
constitute the physical and biological
features essential to conservation of the
Hawaiian monk seal: (1) sandy beaches
preferred by monk seals for pupping
and nursing; (2) marine areas less than
20 m depth adjacent to pupping and
nursing beaches where young pups
learn to forage; (3) marine areas
approximately 20 - 200 m depth in the
MHI, and approximately 20–500 m
depth in the NWHI, preferred by
juvenile and adult monk seals for
foraging; (4) low levels of unnatural
disturbance; and (5) high prey quantity
and quality.
Steps 3 - 5: Steps 3 - 5 of the critical
habitat proposed revision process will
be completed in the forthcoming
proposed rule. In the proposed rule, the
PCEs could differ slightly from the PCEs
identified above, but these identified
PCEs will give the public an idea of
what we are considering. When we
publish our proposed rule, we will
solicit public comments on it and
incorporate comments as appropriate.
References Cited
Amerson, A.B., Jr., and P.C. Shelton.
1976. The natural history of Johnston
Atoll, Central Pacific Ocean: Hawaiian
Monk Seal. Atoll Research Bulletin 192:
384.
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Antonelis, G.A., J.D. Baker, T.C.
Johanos, R.C. Braun, and A.L. Harting.
2006. Hawaiian monk seal ((Monachus
schauinslandi): Status and conservation
issues. Atoll Research Bulletin 543:75–
101.
Bailey, A.M. 1952. The Hawaiian
monk seal. Denver Museum of Natural
History, Museum Pictorial 7:1–32.
Baker, J.D., and T.C. Johanos. 2004.
Abundance of the Hawaiian monk seal
in the main Hawaiian Islands. Biological
Conservation 116: 103–110.
Baker, J.D., C.L. Littnan, and D.W.
Johnston. 2006. Potential effects of sea
level rise on the terrestrial habitats of
endangered and endemic megafauna in
the Northwestern Hawaiian Islands.
Endangered Species Research 2:21–30.
Center for Biological Diversity, Kahea,
and Ocean Conservancy. 2008. Petition
to revise critical habitat for the
Hawaiian monk seal (Monachus
schauinslandi) under the Endangered
Species Act. 41 pp. Available at: https://
www.fpir.noaa.gov/Library/PRD/
Critical%20Habitat/Petition-Monk-SealCH–07–02–08.pdf
Goodman-Lowe, G.D. 1998. Diet of the
Hawaiian monk seal (Monachus
schauinslandi) from the Northwestern
Hawaiian Islands during 1991–1994.
Marine Biology 132:535–546.
Grayson, D.K. 2001. The
archaeological record of human impacts
on animal populations. Journal of World
Prehistory 15:1–68.
Henderson, J.R. and Johanos T.C.
1988. Effects of tagging on weaned
Hawaiian monk seal pups. Wildlife
Society Bulletin 16:312–317.
Hiruki, L.M., W.G. Gilmartin, B.L.
Becker, and I. Stirling. 1993. Wounding
in Hawaiian monk seals (Monachus
schauinslandi). Canadian Journal of
Zoology 71:458–468.
Iverson, S., J. Piche, and W.
Blanchard. 2006. Hawaiian monk seals
and their prey in the Northwestern
Hawaiian Islands: Assessing
characteristics of prey species fatty acid
signatures and consequences for
estimating monk seal diets using
quantitative fatty acid signature analysis
(QFASA). Unpublished report. Pacific
Islands Fisheries Science Center,
Honolulu, HI. 134 p.
Johanos, T.C., B.L. Becker, and T.J.
Ragen. 1994. Annual reproductive cycle
of the female Hawaiian monk seal
(Monachus schauinslandi). Marine
Mammal Science 10:13–30.
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16:52 Jun 11, 2009
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Kenyon, K.W. and D.W. Rice. 1959.
Life history of the Hawaiian monk seal.
Pacific Science 13:215–252.
Littnan, C.L., B.S. Stewart, P.K.
Yochem, and R. Braun. 2007. Survey of
selected pathogens and evaluation of
disease risk factors for endangered
Hawaiian monk seals in the main
Hawaiian Islands. EcoHealth 3:232–244.
National Marine Fisheries Service
(NMFS). 1983. Recovery Plan for the
Hawaiian Monk Seal (Monachus
schauinslandi). NMFS, Silver Spring,
MD.
National Marine Fisheries Service
(NMFS). 2001. May 31, 2001, letter from
Rebecca Lent, Regional Administrator,
Southwest Region, and attachment
‘‘Johnston Atoll and Range of the
Hawaiian Monk Seal’’, 8 p.
National Marine Fisheries Service
(NMFS). 2006. 2006 Stock Assessment
Report for the Hawaiian Monk Seal
(Monachus schauinslandi). Revised 12/
15/2006. NMFS, Silver Spring, MD.
Available at: https://www.nmfs.noaa.gov/
pr/pdfs/sars/po2006sehm-hi.pdf
National Marine Fisheries Service
(NMFS). 2007a. Recovery Plan for the
Hawaiian Monk Seal (Monachus
schauinslandi). Revision. NMFS, Silver
Spring, MD. 165 pp. Available at: https://
www.nmfs.noaa.gov/pr/pdfs/recovery/
hawaiianmonkseal.pdf
National Marine Fisheries Service
(NMFS). 2007b. 2007 Stock Assessment
Report for the Hawaiian Monk Seal
(Monachus schauinslandi). Revised 10/
30/2007. NMFS, Silver Spring, MD.
Available at: https://www.nmfs.noaa.gov/
pr/pdfs/sars/po2007sehm-hi.pdf
National Marine Fisheries Service
(NMFS). 2008a. 2008 Stock Assessment
Report for the Hawaiian Monk Seal
(Monachus schauinslandi). Revised 12/
15/2008. NMFS, Silver Spring, MD.
National Marine Fisheries Service
(NMFS). 2008b. March 18, 2008,
biological opinion on effects of
Implementation of Bottomfish Fishing
Regulations within Federal Waters of
the Main Hawaiian Islands on ESAlisted marine species. Pacific Islands
Regional Office, 35 p.
Parrish, F.A., M.P. Craig, T.J. Ragen,
G.J. Marshall, and B.M. Buhleier. 2000.
Identifying diurnal foraging habitat of
endangered Hawaiian monk seals using
a seal-mounted video camera. Marine
Mammal Science 16:392–412.
Parrish, F.A., K. Abernathy, G.J.
Marshall, and B.M. Buhleier. 2002.
Hawaiian monk seals (Monachus
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schauinslandi) foraging in deepwater
coral beds. Marine Mammal Science
18:244 258.
Parrish, F.A., G.J. Marshall, C.L.
Littnan, M. Heithaus, S. Canja, B.L.
Becker, R.C. Braun, and G.A. Antonelis.
2005. Foraging of juvenile monk seals at
French Frigate Shoals, Hawaii. Marine
Mammal Science. 21:93–107.
Parrish, F.A., G.J. Marshall, B.
Buhleier, and G.A. Antonelis. 2008.
Foraging interaction between monk
seals and large predatory fish in the
Northwestern Hawaiian Islands.
Endangered Species Research 4:299–
3078.
Parrish, F.A. and C.L. Littnan. 2008.
Changing perspectives in Hawaiian
monk seal research using animal-borne
imaging. Marine Technology Society
Journal 41:30–34.
Parrish, F.A. 2009. Do monk seals
exert top-down pressure in subphotic
ecosystems? Marine Mammal Science
25:91–106.
Rosendahl, P.H. 1994. Aboriginal
Hawaiian structural remains and
settlement patterns in the upland
archeological zone at Lapakahi, Island
of Hawaii. Journal of Hawaiian
Archeology (3): 14 - 70.
Schreiber, R.W. and E. Kridler. 1969.
Occurrence of an Hawaiian monk seal
(Monachus schauinslandi) at Johnston
Atoll, Pacific Ocean. Journal of
Mammalogy 50:841–842.
Schultz, J.K., J.D. Baker, R.J. Toonen,
and B.W. Bowen. 2008. Extremely low
genetic diversity in the endangered
Hawaiian monk seal (Monachus
schauinslandi). Journal of Heredity
doi:10.1093/jhered/esn077.
Stewart, B.S., G.A. Antonelis, J.D.
Baker, and P.K.Yochem. 2006. Foraging
biogeography of Hawaiian monk seals in
the Northwestern Hawaiian Islands.
Atoll Research Bulletin 543:131–146.
Westlake, R.L. and W.G. Gilmartin.
1990. Hawaiian monk seal pupping
locations in the Northwestern Hawaiian
Islands. Pacific Science 44:366–383.
All references are available upon
request (see FOR FURTHER INFORMATION
CONTACT).
Authority: 16 U.S.C. 1531 et seq.
Dated: June 8, 2009.
Samuel D. Rauch III,
Deputy Assistant Administrator for
Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. E9–13880 Filed 6–11–09; 8:45 am]
BILLING CODE 3510–22–S
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Agencies
[Federal Register Volume 74, Number 112 (Friday, June 12, 2009)]
[Proposed Rules]
[Pages 27988-27994]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-13880]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric Administration
50 CFR Part 226
[Docket No. 0809161218-9950-02]
RIN 0648-AX23
Endangered and Threatened Species: 12-Month Finding for a
Petition to Revise Critical Habitat for Hawaiian Monk Seal
AGENCY: National Marine Fisheries Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA), Commerce.
ACTION: Notice of 12-month finding.
-----------------------------------------------------------------------
SUMMARY: On July 9, 2008, we (NMFS) received a petition dated July 2,
2008, requesting that we revise the present critical habitat
designation for the Hawaiian monk seal (Monachus schauinslandi) under
the Endangered Species Act (ESA) by expanding the current critical
habitat in the Northwestern Hawaiian Islands, and by designating
additional critical habitat in the main Hawaiian Islands. We have
reviewed, and here provide a summary of the best available information
regarding Hawaiian monk seal biology and habitat use. Based on our
review, we intend to revise the monk seal's critical habitat, and we
are providing our initial thoughts on the habitat features that are
essential to the conservation of this species and describing how we
intend to proceed with the requested critical habitat revision.
ADDRESSES: Requests for copies of this determination should be
addressed to the Assistant Regional Administrator, Protected Resources
Division, NMFS, 1601 Kapiolani Blvd, Honolulu, HI 96814.
[[Page 27989]]
FOR FURTHER INFORMATION CONTACT: Lance Smith at (808) 944-2258, e-mail
lance.smith@noaa.gov; Krista Graham at (808) 944-2238, e-mail
krista.graham@noaa.gov; or Marta Nammack, (301) 713-1401.
SUPPLEMENTARY INFORMATION: Background documents on the biology of the
Hawaiian monk seal, the July 2, 2008, petition requesting revision of
its critical habitat, and documents explaining the critical habitat
designation process, can be downloaded from https://www.fpir.noaa.gov/PRD/prd_index.html, or requested by phone or e-mail from the NMFS
staff in Honolulu (area code 808) listed under ``FOR FURTHER
INFORMATION CONTACT''. The October 3, 2008, 90-day finding in response
to the petition and the information received in response to the 90-day
finding can be viewed at www.regulations.gov by searching for docket
number ``NOAA-NMFS-2008-0290''.
Background
On July 9, 2008, we received a petition dated July 2, 2008, from
the Center for Biological Diversity, Kahea, and the Ocean Conservancy
(Petitioners) to revise the Hawaiian monk seal critical habitat
designation (Center for Biological Diversity et al., 2008) under the
ESA. Currently designated critical habitat is described below in
``Listing Status and Existing Critical Habitat Under the ESA.'' The
Petitioners seek to revise critical habitat by adding the following
areas in the main Hawaiian Islands (MHI): key beach areas, sand spits
and islets, including all beach crest vegetation to its deepest extent
inland, lagoon waters, inner reef waters, and ocean waters out to a
depth of 200 meters. In addition, The Petitioners request that
currently designated critical habitat in the Northwestern Hawaiian
Islands (NWHI) be extended to include Sand Island at Midway, as well as
ocean waters out to a depth of 500 meters (Center for Biological
Diversity et al., 2008).
On October 3, 2008, we published a 90-day finding in response to
the petition, finding that the petition presented substantial
scientific information indicating that a revision to the current
critical habitat designation may be warranted (73 FR 57583; October 3,
2008). The 90-day finding requested that the public submit information
by December 2, 2008, to help us determine whether a revision of
critical habitat is warranted for the Hawaiian monk seal. The purpose
of this 12-month finding is to announce that we intend to proceed with
a revision of critical habitat for the monk seal and to provide details
on the revision process.
In the following sections, we provide information on the Hawaiian
monk seal's listing status and existing critical habitat under the ESA,
population status and trend, Hawaiian monk seal biology, summary of the
information received from the public in response to our 90-day finding
(73 FR 57583; October 3, 2008), our determination that we will proceed
with a revision of critical habitat, and the criteria we intend to use
for the revision.
Listing Status and Existing Critical Habitat Under the ESA
The Hawaiian monk seal (Monachus schauinslandi) was listed as
endangered under the ESA in 1976 (41 FR 33922; November 23, 1976). This
species occurs throughout the Hawaiian Archipelago and on Johnston
Atoll, and has been sighted at other atolls and islands to the south of
Hawaii. In 1986, critical habitat was designated for all beach areas,
sand spits and islets, including all beach crest vegetation to its
deepest extent inland, lagoon waters, inner reef waters, and ocean
waters out to a depth of 10 fathoms (18.3 m) around Kure Atoll, Midway
Islands (except Sand Island), Pearl & Hermes Reef, Lisianski Island,
Laysan Island, Gardner Pinnacles, French Frigate Shoals, Necker Island,
and Nihoa Island in the NWHI (51 FR 16047; April 30, 1986). In 1988,
critical habitat was extended to include Maro Reef and waters around
previously recommended areas out to the 20 fathom (36.6 m) isobath (53
FR 18988; May 26, 1988). A recovery plan was completed in 1983 (NMFS,
1983) and revised in 2007 (NMFS, 2007a). The species is endemic (found
nowhere else) to the Hawaiian Archipelago, and is one of the most
endangered marine mammals in the United States (NMFS, 2007a).
Hawaiian Monk Seal Biology
The Hawaiian monk seal is a mammal in the Order Carnivora, Family
Phocidae, Genus Monachus. Only two other species occur in this genus,
the recently extinct Caribbean monk seal (M. tropicalis) and the
critically endangered Mediterranean monk seal (M. monachus). Following
is an overview of the Hawaiian monk seal's biology, including Range,
Population Status and Trends, Natural History, Habitat, and
Northwestern Hawaiian Islands vs. Main Hawaiian Islands (a description
of differences in monk seal habitat between these two areas).
Range
Hawaiian monk seals are found throughout the Hawaiian Archipelago
and on Johnston Atoll. The six main reproductive sites for the species
are in the NWHI: Kure Atoll, Midway Islands, Pearl and Hermes Reef,
Lisianski Island, Laysan Island, and French Frigate Shoals. Smaller
reproductive sites also occur on Necker Island and Nihoa Island, and
monk seals have been observed at Gardner Pinnacles and Maro Reef. Monk
seals are found throughout the MHI, where births have been documented
on most of the major islands (NMFS, 2001, 2007a). In 1994, we relocated
21 adult male monk seals from the NWHI to the MHI in order to reduce
male aggression and female deaths at Laysan Island, where males greatly
outnumbered females at the time. We have relocated three female monk
seals (a juvenile in 1981, a pup in 1991, and an adult in 2009) from
the MHI to the NWHI. Thus, we have relocated 21 males from the NWHI to
the MHI, and three females from the MHI to the NWHI.
At Johnston Atoll, a tagged yearling male monk seal from Laysan
Island was first seen in July 1968 (Schreiber and Kilder, 1969) and
remained until at least August 1972. In January 1969, an untagged adult
female monk seal arrived on Sand Island, a secondary island within
Johnston Atoll, and gave birth to a female pup. The mother-pup pair
remained on or near the pupping beach until March 1969, when the pup
was weaned and the mother disappeared. The pup remained until 1971 when
it died from a deep flesh wound, probably from a shark attack (Amerson
and Shelton, 1976). In July 1999, a tagged adult female from French
Frigate Shoals arrived at Johnston Atoll and remained there for about a
year (NMFS, 2001).
In addition to the above reported natural occurrences of monk seals
at Johnston Atoll, a 12 male monk seals have been relocated there from
the Hawaiian Archipelago. In 1984, nine adult males were relocated from
the NWHI to Johnston Atoll, because of attacks on adult females and
immature seals. At least three of these males were still at Johnston
Atoll the following year, and at least one male was still there in
1986. In 1989, two adult males were relocated from the NWHI to Johnston
Atoll because they were drowning pups. In 2003, an adult male was
relocated from the MHI to Johnston Atoll because it was habituated to
humans and exhibiting dangerous behavior. No sighting history is
available for the latter three monk seals (NMFS unpublished data).
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Unconfirmed but probable sightings of Hawaiian monk seals outside
the Hawaiian Archipelago and Johnston Atoll have been reported from
Palmyra Atoll (1,800 km south of NWHI) and Wake Island (2,000 km
southwest of NWHI); two seals were sighted on Palmyra Atoll in 1990, a
seal was sighted on Wake Island in early summer 1966, and a tagged seal
was sighted on Wake Island in February 1987 (Westlake and Gilmartin,
1990, NMFS unpublished data). Other more poorly-documented sightings
have also been reported from Bikini Atoll and Mejit Island in the
Marshall Islands (2,400 km southwest of NWHI, NMFS unpublished data).
Population Status and Trends
The best estimate of Hawaiian monk seal total population size is
1,208 seals in 2006 (1,125 in the NWHI, 83 in the MHI; NMFS, 2008a).
Additional population information can be found in the annual Stock
Assessment Reports (e.g., NMFS, 2006, 2007b, 2008a). The first
rangewide beach count surveys of Hawaiian monk seals were conducted in
the late 1950s. Beach counts of juveniles and adults (i.e., all seals
except pups) declined by 66 percent between the years 1958 and 2006
(Figure I.C.6 in NMFS, 2007a). More recently, beach counts declined
rapidly from 1985 to 1993, and then became relatively stable until the
current decline began in 2001. Total abundance at the six primary NWHI
sites (French Frigate Shoals, Laysan, Lisianski, Pearl and Hermes,
Midway, and Kure) is declining at a rate of about four percent per year
(NMFS 2007a, 2007b, 2008a).
Since 2000, many sites have shown indications of decline in
abundance, apparently due to low juvenile survival. The decline at
French Frigate Shoals is of particular consequence to the welfare of
the overall population because this site once accounted for over 50
percent of the total non-pup beach counts in the NWHI. While that
proportion has now dropped to approximately 25 percent of its observed
peak, there are still more seals at French Frigate Shoals than any
other island or atoll. More detail on Hawaiian monk seal population
status and trends in the NWHI is provided in the recovery plan (NMFS,
2007a). As noted above, in 1994, we relocated 21 adult male monk seals
from the NWHI to the MHI in order to reduce male aggression and female
deaths at Laysan Island, where males greatly outnumbered females at the
time. All female monk seals in the MHI occur there naturally. In 2008,
only five of the 21 relocated male monk seals remained in the MHI.
Although monk seals historically occurred throughout the Hawaiian
Archipelago, the majority of the population now occurs in the NWHI.
Human settlement appears to have largely excluded monk seals from the
MHI, although seal bones have been found at archeological sites dating
from 1400 - 1700 (Rosendahl, 1994). In 1900, Hilo residents reported
that solitary monk seals were seen in the area about once every 10
years (Bailey, 1952). From 1928 to 1956, seven monk seal sightings were
documented in the MHI (Kenyon and Rice, 1959), and Niihau residents
reported that seals appeared there in the 1970s. By 1994 there was a
small naturally-occurring population of male and female monk seals in
the MHI. This population appeared to be growing, and at least six pups
had been born (one in 1962, and five between 1988 and 1993). Since the
mid-1990s, an increasing number of documented sightings and annual
births of monk seal pups have occurred in the MHI. Combined aerial and
ground surveys in the MHI counted 45 hauled-out monk seals in 2000, and
52 in 2001 (Baker and Johanos, 2004). Sightings in the MHI tallied 77
individually identifiable monk seals in 2005 (NMFS, 2007b), and 83 in
2006 (NMFS, 2008a). Together, these observations suggest that monk
seals are recolonizing the MHI.
Natural History
Hawaiian monk seals are wide-ranging, air-breathing predators that
forage underwater, preying primarily on small benthic fishes,
cephalopods (e.g., octopus), and crustaceans (Goodman-Lowe, 1998). They
spend the majority of their time in the ocean, where they are highly
mobile and may have very large home ranges (Antonelis et al., 2006).
Monk seals are typical large predators, in that they can rapidly cover
large areas in search of food. Individuals may travel hundreds of miles
in a few days (Littnan et al., 2007) and dive to 500 m (1,600 ft;
Parrish et al., 2002). Monk seals haul out on land to rest, molt, pup
(give birth), and nurse. Resting may also occur at sea or in shallow,
submerged caves. Monk seals are often solitary, both on land and in the
water, but may congregate in favorable haul-out areas (Antonelis et
al., 2006). Adult monk seals reach a length of 2.3 m (7.5 ft) and weigh
up to 273 kg (600 lb). Unlike most other pinnipeds, monk seals
completely molt, whereby the entire layer of pelage (skin and hair) is
shed annually. The old pelage strips away, leaving a dark grey coat
underneath. Pups are black until first molt, and mostly grey
thereafter, although coloration varies by individual and with age. When
monk seals stay at sea for an extensive period, they may develop a red
or green tinge from algal growth on their pelage (Kenyon and Rice,
1959).
It is thought that Hawaiian monk seals have a lifespan of up to 30
years. Females reach breeding age at about 6 to 11 years of age,
depending on their condition, and give birth no more than once
annually. Mating occurs at sea, and gestation is thought to be
approximately 11 months. Monk seal births are most common between
February and August, peaking in March and April at Laysan Island.
Females give birth to a single pup and nurse it for about 6 weeks,
followed by an abrupt weaning, when the mother abandons the pup
(Johanos et al., 1994). At least several months are required for the
pup to learn to forage successfully on its own, during which time it
survives on fat stores built up during nursing, resulting in
considerable weight loss. Juveniles (up to 3 years old) are typically
longer but thinner than recently-weaned pups, and juveniles in the NWHI
typically do not regain their weaning weight until approximately 2
years of age (Johanos et al., 1994). Male aggression, in which a single
male or multiple males repeatedly attempt to mount and mate with a
female or immature seal, is most common where males outnumber females,
and sometimes results in death or severe injury to the targeted seal.
Individual adult males sometimes attack pups in the same manner, also
sometimes killing the pup (Hiruki et al., 1993).
Habitat
While Hawaiian monk seals spend most of their time in the water,
they frequently haul out on land to rest, molt, pup (give birth), and
nurse. Monk seals may remain at sea for several days or more at a time,
but resting on land is necessary to conserve energy. Resting is
commonly on sandy beaches, but may also occur on rocky shores, rock
ledges, emergent reefs, and even shipwrecks (Antonelis et al., 2006).
Monk seals may take shelter from wind and rain under shoreline
vegetation. Resting on land is typically done for a few hours to
several days at a time, after which the monk seal returns to the water
to continue foraging. When ocean conditions are rough, monk seals may
spend a greater proportion of time resting on land. Hauling-out on land
is also required for molting, when old pelage is shed. Molting is an
annual process taking 1 to 2 weeks, during which time the monk seal
usually remains on land (Kenyon and Rice, 1959).
Pupping and nursing areas are usually sandy beaches adjacent to
shallow
[[Page 27991]]
protected water (Westlake and Gilmartin, 1990). Individual females
appear to favor certain pupping locations, returning to them year after
year. Pregnant females come ashore a few days before giving birth to a
pup weighing approximately 16 kg (35 lb). Pups nurse for 5 to 6 weeks
(Johanos et al., 1994), and weigh 50 - 100 kg (110 - 220 lb) at
weaning. During nursing, the mother-pup pair remain close to each
other, and the mother is protective of her pup. Although the pup is
able to swim at birth, nursing is done on land, and the mother-pup pair
usually remain on land for the first few days after the pup is born.
The mother gradually begins swimming with her pup in the shallows,
returning to the general area around the pupping site. As weaning
approaches, the mother-pup pair spend more time in the water, venturing
further away from the pupping site. After weaning, pups typically
remain in the shallows near their nursing areas for several weeks
before venturing into deeper foraging areas (Kenyon and Rice, 1959;
Henderson and Johanos, 1988).
Monk seals are generalists that forage primarily over low-relief
substrates such as sand and talus. Live fish are generally the
preferred prey, and over 150 fish species have been recorded in the
monk seal diet (Iverson et al., 2006). NWHI camera studies have shown
that adult male monk seals forage mainly on sand terraces and talus
slopes 50 - 100 m (160 - 325 ft) deep around their home atoll and
nearby seamounts (Parrish and Littnan, 2008). Premium adult foraging
habitat is comprised of large, loose talus fragments, which the seals
move to reach the hiding prey underneath (Parrish et al., 2000).
Studies in the NWHI (Parrish et al., 2002; Stewart et al., 2006) have
shown that adult monk seals may forage at 300 - 500 m (1,000 - 1,600
ft), sometimes visiting patches of deep corals (Parrish et al., 2002).
Recent surveys of deep fish assemblages across seamounts of the NWHI
show a pattern of reduced fish biomass at sites close to colonies of
monk seals (Parrish, 2009). Juvenile monk seals (1 - 3 years old)
forage both within shallow atoll lagoons 10 - 30 m (30 - 100 ft) and on
deep reef slopes (50 - 100 m/160 - 325 ft), usually over sand rather
than talus. Juvenile seals likely do not yet have the size or
experience to engage in the large talus-foraging behavior exhibited by
adults (Parrish et al., 2005).
Although much less information is available for monk seals in the
MHI, 11 juvenile and adult monk seals were tracked there in 2005 using
satellite-linked radio transmitters showing location but not depth.
This study indicated that seals usually remained in nearshore waters
within the 200 m (650 ft) isobath. As in the NWHI, this study suggested
that monk seals in the MHI forage mainly in deeper, low-relief (talus,
sand) areas, commuting over shallower, high-relief (coral reefs, rock
outcrops) without foraging (Littnan et al., 2007). However, as in the
NWHI, shallow areas adjacent to pupping areas are important for pups to
develop foraging behavior. Otherwise, coral reefs and other high-relief
shallows are not usually primary monk seal foraging habitat. Generally,
juvenile and adult monk seals bypass these shallow high-relief
substrates in transit to their primary foraging areas over low-relief
substrates in deeper water, sometimes making no attempt to hunt the
same fish species in the shallows that they were actively hunting in
the deep (Parrish and Littnan, 2008).
In summary, the physical and biological habitat features that
support resting, reproduction, and foraging are essential for the
conservation of this species. For the Hawaiian monk seal, essential
habitat includes terrestrial and marine areas. Terrestrial areas
include both resting and reproductive habitat. Resting habitat consists
of nearshore or emergent surfaces where monk seals can haul out,
whereas reproductive habitat consists of a subset of resting habitat on
sandy beaches that are also suitable for pupping and nursing. Marine
areas include foraging habitat for pups, juveniles, and adults. Pup
foraging habitat consists of shallow areas adjacent to pupping beaches
where pups become accustomed to the marine environment and begin
learning to forage on their own. Juveniles and adults forage widely,
primarily in deeper areas.
Northwestern Hawaiian Islands vs. Main Hawaiian Islands
The Hawaiian monk seal consists of one population distributed
throughout the Hawaiian Archipelago. That is, there is no evidence that
monk seals occurring in any part of the archipelago are genetically
distinct from those elsewhere in the archipelago (Schultz et al.,
2008). This suggests that the population is genetically well-mixed,
with individual seals sometimes moving between the NWHI and the MHI,
which has been confirmed with resightings of flipper-tagged or
otherwise identifiable (e.g., scar patterns; Littnan et al., 2007).
However, monk seals in the MHI are typically in better physical
condition than those in the NWHI. For example, weaned pups in the MHI
are larger and fatter than those in the NWHI, which is thought to
reflect better foraging conditions in the MHI (Baker and Johanos, 2004;
Baker et al., 2006). Although the NWHI is one of the largest and best-
protected natural areas in the world, and the MHI are populated by over
a million people, the latter appears to currently provide superior monk
seal foraging conditions.
Despite its large human population, the MHI may currently provide
better monk seal foraging conditions than the NWHI because: (1) There
are only about one-tenth the number of seals in the MHI than in the
NWHI, thus the availability of prey may be higher per seal in the MHI
than the NWHI (Baker and Johanos, 2004); and (2) Large sharks, jacks
and other demersal fish compete directly with monk seals, but are much
less abundant in the MHI than the NWHI (Parrish et al., 2008).
Competition is limited between humans and monk seals in the MHI because
seals prefer small (usually < 20 cm/8 in) eels, wrasses, and other
benthic species not commonly sought by fishermen, (Parrish et al.,
2000). However, while foraging conditions are currently better in the
MHI than the NWHI for monk seals, pollution and runoff pose health
hazards to the species in the MHI not found in the NWHI (Littnan et
al., 2007).
As described above in Population Status and Trends, since 1990, the
total number of Hawaiian monk seals has decreased, while simultaneously
the number of monk seals in the MHI appear to have increased (NMFS,
2006, 2007b, 2008a). As described in the above paragraph, foraging
conditions currently appear better in the MHI than in the NWHI (Parrish
et el., 2000, 2008), likely resulting in better physical condition and
higher survival of seals in the MHI than in the NWHI (Baker and
Johanos; 2004; NMFS, 2007a). In addition, sea level rise may reduce or
eliminate monk seal haul-out habitat more rapidly in the low-lying NWHI
than the MHI (Baker et al., 2006). Given the overall downward trend of
the species (see Population Status and Trends above), generally poor
physical condition and survival of seals in the NWHI, and
proportionally greater sea level effects on the NWHI than the MHI, the
MHI appears essential for the survival and recovery of this species.
Summary of Information Received
In our 90-day finding (73 FR 5l7583; October 3, 2008) in response
to the petition (Center for Biological Diversity et al., 2008), we
solicited information from the public pertaining to the Hawaiian monk
seal's essential habitat needs. The 90-day finding, and the information
we received in response to it, can be viewed at www.regulations.gov by
searching for
[[Page 27992]]
docket number ``NOAA-NMFS-2008-0290''. The great majority of the monk
seal habitat-related information received was based on programs and
studies conducted, funded, or supported by NMFS; therefore, we did not
receive any new information on the monk seal's essential habitat needs.
The information received is summarized below.
Comment 1: Over 100 comments argued that the MHI provide essential
habitat for the Hawaiian monk seal because: (1) the MHI component of
the monk seal population has increased in recent years while
simultaneously the overall population has decreased; (2) monk seals in
the MHI are in better physical condition than those in the NWHI; and
(3) monk seal habitat loss is likely to be much more rapid in the NWHI
than in the MHI in the near future due to sea level rise.
Response: We concur that the MHI component of the monk seal
population appears to have increased in recent years while
simultaneously the overall population has decreased (see ``Population
Size and Trends'' above), that monk seals in the MHI are in better
physical condition than those in the NWHI, and that monk seal haul-out
habitat loss is likely to be more rapid in the NWHI than in the MHI in
the future due to sea level rise (see ``Northwestern Hawaiian Islands
vs. Main Hawaiian Islands'' above). For these three reasons, and also
because of the current precarious state of the Hawaiian monk seal, we
agree that monk seal habitat within the MHI is essential for the
survival and recovery of the species.
Comment 2: Several comments argued that the MHI do not provide
essential habitat for the Hawaiian monk seal, because: (1) monk seals
are not indigenous to the MHI; and (2) various human threats to monk
seals in the MHI outweigh benefits to the species of MHI habitat.
Response: Little evidence has been found that monk seals occurred
in the MHI before the arrival of humans approximately 2,000 years ago,
or during pre-European times before the late 1700s. However, before the
arrival of humans, monk seal remains would typically have occurred on
or near coastlines where wave action and erosion likely would have
prevented preservation of remains. After the arrival of humans, monk
seals may have been consumed by humans, in which case monk seal bones
would likely occur in middens. However, if the seals were quickly
extirpated after the arrival of humans, this would reduce the
likelihood of finding bone fragment evidence in middens. An
archeological dig of a midden on the Big Island identified monk seal
bones, and estimated that the bones were deposited during the years
1400 to 1700 (Rosendahl, 1994). Furthermore, monk seals commonly travel
long distances between atolls or islands, and even between the NWHI and
MHI (Littnan et al., 2007). Thus, before the arrival of humans, it is
highly unlikely that monk seals occurred only in the NWHI, while the
MHI were vacant of both monk seals and humans. Finally, large, easily-
hunted animals such as seals are typically extirpated or driven to
extinction when humans arrive in an area for the first time (Grayson,
2001). Arrival of humans in Hawaii likely resulted in a rapid reduction
in monk seal numbers in the MHI, such that the species was mostly
restricted to the NWHI until recently (Baker and Johanos, 2004). For
these reasons, we believe that the Hawaiian monk seal commonly occurred
in the MHI before the arrival of humans, and that this species is
indigenous to at least the entire Hawaiian Archipelago.
We agree that the Hawaiian monk seal faces a multitude of human
threats in the MHI. The recovery plan identifies the most serious human
threats to monk seals in the MHI as infectious diseases, fisheries
interactions, habitat loss, and human interactions (NMFS, 2007a). In
the MHI, monk seals forage near shore, and they haul out on beaches
near sources of pathogens associated with human population centers,
sewage spills, and stream mouths. Of 12 dead monk seals that were
thoroughly necropsied in the MHI between 1996 and 2006, four appeared
to have died of infectious disease (Littnan et al., 2007). In the MHI
from 1989 to 2007, 44 monk seals were confirmed to be hooked by fishing
gear (one of which died, possibly from the hooking), another five
entangled in lay gillnets (three of which drowned in the gillnets), and
one seal hooked and entangled (but survived). Many hooks are removed
from monk seals by the monk seal response program, most often resulting
in healing of the wound and recovery of the monk seal. However,
entanglement in lay gillnets often results in the drowning of the monk
seal (NMFS, 2008b). Monk seal haul-out beaches in the MHI are being
degraded or lost by development adjacent to the beaches, and increasing
human activity on the beaches. The high and ever-increasing human use
of MHI beaches and coastlines results in humans frequently interacting
with monk seals, both unintentionally and intentionally (NMFS, 2007a).
However, despite the numerous anthropogenic threats to monk seals in
the MHI, the MHI component of the monk seal population appears to have
increased in recent years, and monk seals in the MHI are generally in
good physical condition. In contrast, the NWHI component of the monk
seal population continues to decrease, and monk seals in the NWHI are
often in poor physical condition (see ``Population Size and Trends''
and ``Northwestern Hawaiian Islands vs. Main Hawaiian Islands'' above).
Thus, although monk seals are more often exposed to infectious diseases
in the MHI than in the NWHI, the MHI appear to currently provide a
favorable environment for monk seals. In addition, the loss of monk
seal haul-out habitat is likely to occur more rapidly in the NWHI than
the MHI due to sea level rise (see ``Northwestern Hawaiian Islands vs.
Main Hawaiian Islands'' above). For these reasons, we believe that the
benefits of MHI habitat to the monk seal outweigh the various human
threats to monk seals in the MHI.
Comment 3: Over 100 comments argued that areas out to a depth of
500 m (1,625 ft) in the NWHI provide essential foraging habitat for the
Hawaiian monk seal.
Response: As discussed above in ``Habitat,'' studies in the NWHI
have documented adult monk seal foraging to a maximum depth of
approximately 500 m (1,600 ft; Parrish et al., 2002; Stewart et al.,
2006). The relative importance of these deep foraging areas, compared
to more frequently-used shallower areas, is currently unknown.
Comment 4: Several comments did not provide any information about
habitat use by the Hawaiian monk seal, but rather expressed opinions
about the effects of revising monk seal critical habitat on various
human activities, such as beach use, fishing, economics, national
security, and natural resource management.
Response: The economic, national security, and other effects of
revising monk seal critical habitat will be addressed in the
forthcoming proposed rule.
12-Month Determination on Revision of Critical Habitat
Since critical habitat for the Hawaiian monk seal was designated in
1986 (51 FR 16047; April 30, 1986) and revised in 1988 (53 FR 18988;
May 26, 1988), a great deal of new information has become available
regarding habitat use by this species, such as the literature cited in
the petition (Center for Biological Diversity et al., 2008) and in the
Recovery Plan (NMFS, 2007a). For example, studies of monk seal foraging
made possible by new technology (e.g.,
[[Page 27993]]
Parrish et al. 2000, 2002, 2005, 2008; Littnan et al., 2007) have
resulted in substantial progress since 1988 in understanding how this
species uses foraging habitat (Parrish and Littnan, 2008). Also, since
critical habitat was designated in 1988, monk seals appear to have
begun recolonizing the MHI (Baker and Johanos, 2004; Baker et al.,
2006; NMFS, 2007a). Other information has also become available about
other aspects of monk seal life history and habitat use (summarized in
NMFS, 2007a). Because of this new information regarding habitat use by
the Hawaiian monk seal that has become available since critical habitat
for the species was revised in 1988 (53 FR 18988; May 26, 1988), we
will proceed with a revision of critical habitat for the species.
How Does NMFS Intend To Proceed?
We intend to undertake rulemaking to revise critical habitat for
the Hawaiian monk seal. Critical habitat is defined by section 3 of the
ESA as ``(i) the specific areas within the geographical area occupied
by the species, at the time it is listed in accordance with the
provisions of section 1533 of this title, on which are found those
physical or biological features (I) essential to the conservation of
the species and (II) which may require special management
considerations or protection; and (ii) specific areas outside the
geographical area occupied by the species at the time it is listed in
accordance with the provisions of section 1533 of this title, upon a
determination by the Secretary that such areas are essential for the
conservation of the species.'' Further, our critical habitat
regulations (50 CFR 424.12(c)) state that critical habitat will be
defined by specific limits using reference points and lines on standard
topographic maps of the area. Finally, section 4(b)(2) of the ESA
requires that we consider economic, national security, and other
impacts of designating critical habitat before designating critical
habitat.
Based on the above definition and guidance, the following steps
will be followed to propose the revision of designated critical habitat
for the Hawaiian monk seal: (1) Determine the geographical area
occupied by the species at the time of listing; (2) Identify the
physical or biological features essential to the conservation of the
species; (3) Delineate areas within the geographical area occupied by
the species that contain these features, and that may require special
management considerations or protections; (4) Delineate any areas
outside of the geographical area occupied by the species that are
essential for the conservation of the species; and (5) Conduct
economic, national security, and other analyses to determine if any
areas identified in steps 3 and 4 could be excluded from critical
habitat consideration under section 4(b)(2) of the ESA. Steps 1 and 2
above are included in this 12-month finding, as described below. Steps
3 - 5 will be completed in the forthcoming proposed rule.
Step 1: Determine Geographical Area Occupied by the Species at the
Time of Listing: The final rule listing the Hawaiian monk seal as
endangered, published on November 23, 1976 (41 FR 51611), stated that
the ``Hawaiian monk seal is found throughout the Hawaiian
Archipelago,'' with no mention of areas outside the archipelago. For
reasons described above in ``Range,'' in 2001, we determined that
Johnston Atoll is within the range of the Hawaiian monk seal (NMFS,
2001). Therefore, the geographical area occupied by the Hawaiian monk
seal at the time of listing (1976) is considered to be the Hawaiian
Archipelago and Johnston Atoll.
Step 2: Identify Physical or Biological Features Essential to
Conservation: In this step, the physical and biological features
essential to conservation are identified (hereafter referred to as
``essential features''). Section 3 of the ESA (16 U.S.C. 1532(3))
defines the terms ``conserve,'' ``conserving,'' and ``conservation'' to
mean: ``to use, and the use of, all methods and procedures which are
necessary to bring any endangered species or threatened species to the
point at which the measures provided pursuant to this chapter are no
longer necessary.'' Our critical habitat regulations (50 CFR 424.12(b))
state that essential features ``include, but are not limited to the
following: (1) Space for individual and population growth, and for
normal behavior; (2) Food, water, air, light, minerals or other
nutritional or physiological requirements; (3) Cover or shelter; (4)
Sites for breeding, reproduction, rearing of offspring, germination, or
seed dispersal; and generally; (5) Habitats that are protected from
disturbance or are representative of the historic geographical and
ecological distributions of a species.''
The regulations also instruct us to ``focus on the principal
biological or physical constituent elements within the defined area
that are essential to the conservation of the species. Known primary
constituent elements shall be listed with the critical habitat
description'' (50 CFR 424.12(b)). Thus, the essential features will be
defined here in terms of primary constituent elements (PCEs). The PCEs
can include sites used by the listed species for resting, reproduction,
and feeding (examples given in the regulations include ``nesting
grounds, spawning sites, feeding sites''), and physical features of the
species' habitat (examples given in the regulations include
``geological formation, vegetation type, tide, and specific soil
types''; 50 CFR 424.12(b)).
As described above in ``Habitat,'' the physical and biological
habitat features that support resting, molting, reproduction, and
foraging are essential for the conservation of this species. For the
Hawaiian monk seal, essential habitat includes terrestrial and marine
areas. Terrestrial areas include resting, molting, and reproductive
habitat. Resting and molting habitat consists of nearshore or emergent
surfaces where monk seals can haul out, whereas reproductive habitat
consists of a subset of resting and molting habitat (i.e., sandy
beaches suitable for pupping and nursing). Marine areas include
foraging habitat for pups, juveniles, and adults. Pup foraging habitat
consists of shallow areas adjacent to pupping beaches where pups become
accustomed to the marine environment and begin learning to forage on
their own. Juveniles and adults forage widely, primarily in deeper
areas. Thus, at this time, we believe that the following PCEs
constitute the physical and biological features essential to
conservation of the Hawaiian monk seal: (1) sandy beaches preferred by
monk seals for pupping and nursing; (2) marine areas less than 20 m
depth adjacent to pupping and nursing beaches where young pups learn to
forage; (3) marine areas approximately 20 - 200 m depth in the MHI, and
approximately 20-500 m depth in the NWHI, preferred by juvenile and
adult monk seals for foraging; (4) low levels of unnatural disturbance;
and (5) high prey quantity and quality.
Steps 3 - 5: Steps 3 - 5 of the critical habitat proposed revision
process will be completed in the forthcoming proposed rule. In the
proposed rule, the PCEs could differ slightly from the PCEs identified
above, but these identified PCEs will give the public an idea of what
we are considering. When we publish our proposed rule, we will solicit
public comments on it and incorporate comments as appropriate.
References Cited
Amerson, A.B., Jr., and P.C. Shelton. 1976. The natural history of
Johnston Atoll, Central Pacific Ocean: Hawaiian Monk Seal. Atoll
Research Bulletin 192: 384.
[[Page 27994]]
Antonelis, G.A., J.D. Baker, T.C. Johanos, R.C. Braun, and A.L.
Harting. 2006. Hawaiian monk seal ((Monachus schauinslandi): Status and
conservation issues. Atoll Research Bulletin 543:75-101.
Bailey, A.M. 1952. The Hawaiian monk seal. Denver Museum of Natural
History, Museum Pictorial 7:1-32.
Baker, J.D., and T.C. Johanos. 2004. Abundance of the Hawaiian monk
seal in the main Hawaiian Islands. Biological Conservation 116: 103-
110.
Baker, J.D., C.L. Littnan, and D.W. Johnston. 2006. Potential
effects of sea level rise on the terrestrial habitats of endangered and
endemic megafauna in the Northwestern Hawaiian Islands. Endangered
Species Research 2:21-30.
Center for Biological Diversity, Kahea, and Ocean Conservancy.
2008. Petition to revise critical habitat for the Hawaiian monk seal
(Monachus schauinslandi) under the Endangered Species Act. 41 pp.
Available at: https://www.fpir.noaa.gov/Library/PRD/Critical%20Habitat/Petition-Monk-Seal-CH-07-02-08.pdf
Goodman-Lowe, G.D. 1998. Diet of the Hawaiian monk seal (Monachus
schauinslandi) from the Northwestern Hawaiian Islands during 1991-1994.
Marine Biology 132:535-546.
Grayson, D.K. 2001. The archaeological record of human impacts on
animal populations. Journal of World Prehistory 15:1-68.
Henderson, J.R. and Johanos T.C. 1988. Effects of tagging on weaned
Hawaiian monk seal pups. Wildlife Society Bulletin 16:312-317.
Hiruki, L.M., W.G. Gilmartin, B.L. Becker, and I. Stirling. 1993.
Wounding in Hawaiian monk seals (Monachus schauinslandi). Canadian
Journal of Zoology 71:458-468.
Iverson, S., J. Piche, and W. Blanchard. 2006. Hawaiian monk seals
and their prey in the Northwestern Hawaiian Islands: Assessing
characteristics of prey species fatty acid signatures and consequences
for estimating monk seal diets using quantitative fatty acid signature
analysis (QFASA). Unpublished report. Pacific Islands Fisheries Science
Center, Honolulu, HI. 134 p.
Johanos, T.C., B.L. Becker, and T.J. Ragen. 1994. Annual
reproductive cycle of the female Hawaiian monk seal (Monachus
schauinslandi). Marine Mammal Science 10:13-30.
Kenyon, K.W. and D.W. Rice. 1959. Life history of the Hawaiian monk
seal. Pacific Science 13:215-252.
Littnan, C.L., B.S. Stewart, P.K. Yochem, and R. Braun. 2007.
Survey of selected pathogens and evaluation of disease risk factors for
endangered Hawaiian monk seals in the main Hawaiian Islands. EcoHealth
3:232-244.
National Marine Fisheries Service (NMFS). 1983. Recovery Plan for
the Hawaiian Monk Seal (Monachus schauinslandi). NMFS, Silver Spring,
MD.
National Marine Fisheries Service (NMFS). 2001. May 31, 2001,
letter from Rebecca Lent, Regional Administrator, Southwest Region, and
attachment ``Johnston Atoll and Range of the Hawaiian Monk Seal'', 8 p.
National Marine Fisheries Service (NMFS). 2006. 2006 Stock
Assessment Report for the Hawaiian Monk Seal (Monachus schauinslandi).
Revised 12/15/2006. NMFS, Silver Spring, MD. Available at: https://www.nmfs.noaa.gov/pr/pdfs/sars/po2006sehm-hi.pdf
National Marine Fisheries Service (NMFS). 2007a. Recovery Plan for
the Hawaiian Monk Seal (Monachus schauinslandi). Revision. NMFS, Silver
Spring, MD. 165 pp. Available at: https://www.nmfs.noaa.gov/pr/pdfs/recovery/hawaiianmonkseal.pdf
National Marine Fisheries Service (NMFS). 2007b. 2007 Stock
Assessment Report for the Hawaiian Monk Seal (Monachus schauinslandi).
Revised 10/30/2007. NMFS, Silver Spring, MD. Available at: https://www.nmfs.noaa.gov/pr/pdfs/sars/po2007sehm-hi.pdf
National Marine Fisheries Service (NMFS). 2008a. 2008 Stock
Assessment Report for the Hawaiian Monk Seal (Monachus schauinslandi).
Revised 12/15/2008. NMFS, Silver Spring, MD.
National Marine Fisheries Service (NMFS). 2008b. March 18, 2008,
biological opinion on effects of Implementation of Bottomfish Fishing
Regulations within Federal Waters of the Main Hawaiian Islands on ESA-
listed marine species. Pacific Islands Regional Office, 35 p.
Parrish, F.A., M.P. Craig, T.J. Ragen, G.J. Marshall, and B.M.
Buhleier. 2000. Identifying diurnal foraging habitat of endangered
Hawaiian monk seals using a seal-mounted video camera. Marine Mammal
Science 16:392-412.
Parrish, F.A., K. Abernathy, G.J. Marshall, and B.M. Buhleier.
2002. Hawaiian monk seals (Monachus schauinslandi) foraging in
deepwater coral beds. Marine Mammal Science 18:244 258.
Parrish, F.A., G.J. Marshall, C.L. Littnan, M. Heithaus, S. Canja,
B.L. Becker, R.C. Braun, and G.A. Antonelis. 2005. Foraging of juvenile
monk seals at French Frigate Shoals, Hawaii. Marine Mammal Science.
21:93-107.
Parrish, F.A., G.J. Marshall, B. Buhleier, and G.A. Antonelis.
2008. Foraging interaction between monk seals and large predatory fish
in the Northwestern Hawaiian Islands. Endangered Species Research
4:299-3078.
Parrish, F.A. and C.L. Littnan. 2008. Changing perspectives in
Hawaiian monk seal research using animal-borne imaging. Marine
Technology Society Journal 41:30-34.
Parrish, F.A. 2009. Do monk seals exert top-down pressure in
subphotic ecosystems? Marine Mammal Science 25:91-106.
Rosendahl, P.H. 1994. Aboriginal Hawaiian structural remains and
settlement patterns in the upland archeological zone at Lapakahi,
Island of Hawaii. Journal of Hawaiian Archeology (3): 14 - 70.
Schreiber, R.W. and E. Kridler. 1969. Occurrence of an Hawaiian
monk seal (Monachus schauinslandi) at Johnston Atoll, Pacific Ocean.
Journal of Mammalogy 50:841-842.
Schultz, J.K., J.D. Baker, R.J. Toonen, and B.W. Bowen. 2008.
Extremely low genetic diversity in the endangered Hawaiian monk seal
(Monachus schauinslandi). Journal of Heredity doi:10.1093/jhered/
esn077.
Stewart, B.S., G.A. Antonelis, J.D. Baker, and P.K.Yochem. 2006.
Foraging biogeography of Hawaiian monk seals in the Northwestern
Hawaiian Islands. Atoll Research Bulletin 543:131-146.
Westlake, R.L. and W.G. Gilmartin. 1990. Hawaiian monk seal pupping
locations in the Northwestern Hawaiian Islands. Pacific Science 44:366-
383.
All references are available upon request (see FOR FURTHER
INFORMATION CONTACT).
Authority: 16 U.S.C. 1531 et seq.
Dated: June 8, 2009.
Samuel D. Rauch III,
Deputy Assistant Administrator for Regulatory Programs, National Marine
Fisheries Service.
[FR Doc. E9-13880 Filed 6-11-09; 8:45 am]
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