Endangered and Threatened Wildlife and Plants; Removal of the Brown Pelican (Pelecanus occidentalis) From the Federal List of Endangered and Threatened Wildlife, 59444-59472 [E9-27402]
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Federal Register / Vol. 74, No. 220 / Tuesday, November 17, 2009 / Rules and Regulations
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS–R2–ES–2008–0025 ; 92220–1113–
0000–C6]
RIN 1018–AV28
Endangered and Threatened Wildlife
and Plants; Removal of the Brown
Pelican (Pelecanus occidentalis) From
the Federal List of Endangered and
Threatened Wildlife
AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Final rule.
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SUMMARY: Under the authority of the
Endangered Species Act of 1973, as
amended (Act), we, the U.S. Fish and
Wildlife Service (Service), are removing
the brown pelican (Pelecanus
occidentalis) from the Federal List of
Endangered and Threatened Wildlife
due to recovery. This action is based on
a review of the best available scientific
and commercial data, which indicate
that the species is no longer in danger
of extinction, or likely to become so
within the foreseeable future. The
brown pelican will remain protected
under the provisions of the Migratory
Bird Treaty Act.
DATES: The effective date of this rule is
December 17, 2009.
ADDRESSES: This final rule is available
on the Internet at https://
www.regulations.gov and https://
www.fws.gov/southwest/es/Library/.
Supporting documentation used in
preparing this final rule will be
available for public inspection, by
appointment, during normal business
hours, at the Service’s Clear Lake
Ecological Services Field Office, 17629
El Camino Real #211, Houston, Texas
77058–3051.
FOR FURTHER INFORMATION CONTACT:
Steve Parris, Field Supervisor, U.S. Fish
and Wildlife Service, Clear Lake
Ecological Services Field Office, 17629
El Camino Real #211, Houston, Texas
77058–3051; telephone 281/286–8282;
facsimile 281/488–5882. If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 800–877–8339.
SUPPLEMENTARY INFORMATION:
Background
Brown pelican (Pelecanus
occidentalis) populations currently
listed under the Endangered Species Act
of 1973, as amended (Act; 16 U.S.C.
1531 et seq.) occur in primarily coastal
marine and estuarine (where fresh and
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salt water intermingle) environments
along the coast of the Gulf of Mexico
from Mississippi to Texas and the coast
of Mexico; along the Caribbean coast
from Mexico south to Venezuela; along
the Pacific Coast from British Columbia,
Canada, south through Mexico into
Central and South America; and in the
West Indies, and are occasionally
sighted throughout the United States
(Shields 2002, pp. 2–4). Brown pelicans
remain in residence throughout the
breeding range, but some segments of
many populations migrate annually
after breeding (Shields 2002, p. 6).
Overall, the brown pelican continues to
occur throughout its historical range
(Shields 2002, pp. 4–5). This rule
includes biological and life history
information for the brown pelican
relevant to the delisting. Additional
information about the brown pelican’s
biology and life history can be found in
the Birds of North America, No. 609
(Shields 2002, pp. 1–36).
This rule applies to the entire listed
species, which includes all brown
pelican (Pelecanus occidentalis)
subspecies. The species Pelecanus
occidentalis is generally recognized as
consisting of six subspecies: (1) P. o.
occidentalis (Linnaeus, 1766: West
Indies and the Caribbean Coast of South
America, occasionally wanders to coasts
of Mexico and Florida), (2) P. o.
carolinensis (Gmelin, 1798: Atlantic and
Gulf coasts of the United States and
Mexico; Caribbean Coast of Mexico
south to Venezuela, South America;
Pacific Coast from southern Mexico to
northern Peru, South America), (3) P. o.
californicus (Ridgeway, 1884: California
south to Colima, Mexico, including Gulf
of California), (4) P. o. urinator
(Wetmore, 1945: Galapagos Islands), (5)
P. o. murphyi (Wetmore, 1945: Ecuador
and Pacific Coast of Colombia), and (6)
P. o. thagus (Molina, 1782: Peru and
Chile). Recognition of brown pelican
subspecies is based largely on relative
size and color of plumage and soft parts
(for example, the bill, legs, and feet).
The distributional limits of the brown
pelican subspecies are poorly known, so
the geographic descriptions of their
ranges are approximate and may not be
adequate to assign subspecies
designations. Additionally, some
authors elevate the Peruvian subspecies
to a separate species, Peruvian pelican
(P. thagus) (see Remsen et al. 2009).
However, the taxonomy of the brown
pelican subspecies has not been
critically reviewed for many years, and
the classification followed by the
American Ornithologists’ Union
(American Ornithologists’ Union 1957,
pp. 29–30) and by Palmer (1962, pp.
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274–276) is based on Wetmore’s (1945,
pp. 577–586) review, which was based
on few specimens from a limited
portion of the range. Remsen et al.
(2009) does not present a
comprehensive taxonomic treatment of
all brown pelicans, but rather, relies on
already noted morphological differences
to propose that P. o. thagus be
recognized as a full species. Additional
taxonomic review of all brown pelicans
would be needed to further elucidate
the relationships and distributions of
the six described subspecies. The
original listing of the brown pelican
included the species throughout its
range and covered all six of the
subspecies described above. This rule
continues that taxonomic treatment,
including the Peruvian brown pelican
(P. o. thagus).
Previous Federal Actions
On February 20, 2008, we published
a 12-month petition finding and
proposed rule to remove the brown
pelican from the Federal List of
Endangered and Threatened Wildlife
(73 FR 9408). We solicited data and
comments from the public on the
proposed rule. The comment period
opened on February 20, 2008, and
closed on April 21, 2008. Note that this
proposed rule addresses the status of
brown pelicans throughout their range
except where previously delisted along
the Atlantic Coast of the United States,
in Florida, and in Alabama (50 FR 4938;
February 4, 1985). For more information
on previous Federal actions concerning
the brown pelican, please refer to the
proposed rule published in the Federal
Register on February 20, 2008 (73 FR
9408).
Distribution and Population Estimates
Information on population estimates
below is arranged geographically for
convenience and to present a logical
organization of the information. These
broad geographic areas do not
necessarily represent populations or
other biologically based groupings. The
six subspecies described above are not
used to organize the following
information because distributional
limits of the subspecies are poorly
known, especially in Central and South
America. Additionally, the broad
overlap in wintering and breeding
ranges among the subspecies introduces
considerable uncertainty in assigning
subspecies designations in portions of
the species range (Shields 2002, p. 5).
Because the brown pelican is a wideranging, mobile species, is migratory
throughout much of its range, and may
shift its breeding or wintering areas or
distribution in response to local
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conditions, it is difficult to define local
populations of the species. Much of the
population estimate information below
is given at the scale of individual
countries, which may not correspond
with actual biological populations,
particularly for smaller countries that
may represent only a fraction of the
species’ range. Direct comparison of all
the estimates provided below is difficult
because methods used to derive
population estimates are not always
reported, some population estimates are
given as broad ranges, and some do not
specify whether the estimates are for
breeding birds or include nonbreeding
birds as well. However, the information
does indicate the broad distribution of
the species and reflects the large global
population estimate of more than
620,000 birds, which does not include
previously delisted birds along the
Atlantic coast of the United States, in
Florida, or in Alabama (Service 2007a,
pp. 44–45).
Gulf of Mexico Coast
Mississippi.—Turcotte and Watts
(1999, pp. 84–86) consider the brown
pelican a permanent resident of the
Mississippi coast, even though there are
no records of nesting brown pelicans in
Mississippi. Brown pelicans are
currently not known to breed in
Mississippi, but the annual Christmas
Bird Counts have documented wintering
brown pelicans in Mississippi since
1985 (National Audubon Society 2009,
pp. 1–3). The most recent counts over
the winter of 2008–2009 sighted 372
brown pelicans (National Audubon
Society 2009, p. 3).
Louisiana.—Before 1920, brown
pelicans were estimated to have
numbered between 50,000 and 85,000 in
Louisiana (King et al. 1977a, pp. 417,
419). By 1963, the brown pelican had
completely disappeared from Louisiana
(Williams and Martin 1968, p. 130). A
reintroduction program was conducted
between 1968 and 1980. During this
period, 1,276 nestling brown pelicans
were transplanted from colonies in
Florida to coastal Louisiana (McNease et
al. 1984, p. 169). After the initiation of
the reintroduction, the population
reached a total number of 16,405
successful nests and 34,641 young
produced in 2001 (Holm et al. 2003, p.
432).
In 2003, the number of nesting
colonies increased, but numbers of
successful nests decreased to 13,044 due
to four severe storms that eroded
portions of some nest islands and
destroyed some late nests in various
colonies (Hess and Linscombe 2003,
Table 2). According to surveys
conducted by the Louisiana Department
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of Wildlife and Fisheries (LDWF), the
population appeared to recover from
these impacts and a peak of 16,501
successful nests producing 39,021
fledglings was recorded in 2004 (LDWF
2006, p. 1; Hess and Linscombe 2006, p.
13). However, tropical storms in 2004
resulted in the loss of three nesting
islands east of the Mississippi River
and, after storm events in late 2005,
LDWF surveys detected 25,289
fledglings (Hess and Linscombe 2006, p.
13). Surveys in 2006 detected 8,036
successful nests in 15 colonies,
producing 17,566 fledglings with an
average of 2.1 fledglings per successful
nest (Hess and Linscombe 2007, pp. 1,
4). In 2007, there were 14 colonies that
produced 24,085 fledglings with an
average of 2.2 fledglings per nest (LDWF
2008, pp. 3, 6).
Hess and Linscombe (2007, p. 4)
concluded that the brown pelican
population in Louisiana is maintaining
sustained growth despite lower
fledgling production in 2005 and 2006
(a decrease of 31 percent from 2005 to
2006). Fledgling production has
increased 37.1 percent from 2006 to
2007 (LDWF 2008, p. 5). Numbers of
successful nests are not directly
comparable to numbers of individuals
in historic estimates because they do not
account for immature or nonbreeding
individuals or provide an index of
population size in years when breeding
success is low due to factors such as
weather and food availability. However,
numbers of successful nests and
fledglings produced annually since 1993
(Hess and Linscombe 2007, p. 4; LDWF
2008, p. 4) do indicate continued
nesting and successful fledging of young
sufficient to sustain a viable population
in Louisiana. See ‘‘Storm effects,
weather, and erosion impacts to habitat’’
under Factor A for further discussion of
effects of storms.
Texas.—Brown pelicans historically
numbered around 5,000 in Texas but
began to decline in the 1920s and 1930s,
presumably due to shooting and
destruction of nests (King et al. 1977a,
p. 419). According to King et al. (1977a,
p. 422), there were no reports of brown
pelicans nesting in Texas in 1964 or
1966. There were two known nesting
attempts in 1965, but the success of
these nests is not known. Annual aerial
and ground surveys of traditional
nesting colonies conducted in Texas
during the period 1967 to 1974
indicated that only two to seven pairs
attempted to breed in each of these
years. Only 40 young were documented
fledging during this entire 8-year period
(King et al. 1977a, p. 422).
The Texas Colonial Waterbird Census
has tracked population trends in Texas
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59445
for the brown pelican since 1973
(Service 2006, p. 5). Although the Texas
population of brown pelicans did not
experience the total reproductive failure
recorded in Louisiana, the first year
(1973) of information from the Texas
census identified only one nesting
colony with six breeding pairs in the
State. Since that time, there was a
gradual increase through 1993 when
there were 530 breeding pairs in two
nesting colonies; in 1994, there was a
substantial increase to 1,751 breeding
pairs in three nesting colonies (Service
2006, pp. 3–5). Since then, the overall
increasing trend has continued with
some year-to-year variation (Service
2006, pp. 2–3). The most recent
complete count of breeding birds in
Texas occurred in 2008 and reported
6,136 pairs (Service 2009c). This
number equates to 12,272 breeding
birds, which is substantially greater
than historical population estimates for
Texas.
Gulf Coast of Mexico.—Very little
information is available about the status
of the brown pelican along the Gulf
Coast in Mexico. Aerial surveys
indicated that brown pelicans in Mexico
were virtually absent as a breeding
species along the Gulf of Mexico north
of Veracruz by 1968 (Service 1979, p.
10). An aerial survey conducted in
March 1986 along this same stretch of
coast counted 2,270 birds, down from
4,250 birds estimated in counts
conducted between December 1979 and
January 1980 (Blankenship 1987, p. 2).
However, the counts in 1986 and in
1980 differed in the areas covered and
timing of counts and represent only two
data points, so it is difficult to compare
the earlier and later counts. A recent
survey of colonial waterbirds at Laguna
Madre de Tamaulipas did not locate
brown pelicans (Pronatura and
Audubon Texas 2008), although brown
pelicans were not sighted there during
the 1986 aerial surveys either
(Blankenship 1987, Table 1). No other
recent information for this portion of the
species’ range was found, so no
conclusions on population trends of the
brown pelican for the Mexican portion
of the Gulf Coast can be drawn.
Summary of Gulf of Mexico Coast.—
Along the U.S. Gulf Coast, brown
pelican populations, while experiencing
some periodic or local declines, have
increased dramatically from a point of
near disappearance in the 1960s and
70s. Brown pelicans were present along
the Gulf Coast of Mexico in 1986, but
we currently lack recent information on
the status of the species in this portion
of its range.
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West Indies
The West Indies refers to a crescentshaped group of islands occurring in the
Caribbean Sea consisting of the
Bahamas, the Greater Antilles
(including Cuba, Jamaica, Haiti, the
Dominican Republic, and Puerto Rico),
and the Lesser Antilles (a group of
island countries forming an arc from the
U.S. Virgin Islands on its northwest end
southeast to Grenada). Van Halewyn
and Norton (1984, p. 201) summarized
the breeding distribution of brown
pelicans throughout the Caribbean
region and noted at least 23 sites where
the species was reliably reported nesting
in the islands of the West Indies at some
time since 1950. Based on the most
recent estimates available at the time,
van Halewyn and Norton (1984, p. 201)
documented more than 2,000 breeding
pairs throughout the West Indies. More
recently, Collazo et al. (2000, p. 42)
estimated the minimum number of
brown pelicans throughout the West
Indies at 1,500 breeding pairs, and
Bradley and Norton (2009, p. 275)
estimated the West Indian population at
1,630 breeding pairs. Raffaele et al.
(1998, pp. 224–225) describe the brown
pelican as ‘‘A common year-round
resident in the southern Bahamas,
Greater Antilles and locally in the
northern Lesser Antilles east to
Montserrat. It is common to rare through
the rest of the West Indies with some
birds wandering between islands.’’
In a search for additional seabird
breeding colonies in the Lesser Antilles,
Collier et al. (2003, pp. 112–113) did not
find brown pelicans nesting on
Anguilla, Saba, and Dominica. In an
attempt to survey seabirds in St. Vincent
and the Grenadines, Hayes (2002, p. 51)
found brown pelicans in the central
Grenadines. He notes that brown
pelicans were once considered common
in the Grenadines and suggests that a
small nesting colony may exist there,
although there is no historical record of
nesting.
Anguilla, Montserrat, Jamaica, the
Bahamas, and Antigua.—Recent
information presented in Bradley and
Norton (2009, p. 275) reports 21
breeding pairs in Anguilla, 14 in
Montserrat, greater than 150 in Jamaica,
50 in the Bahamas, and 53 in Antigua.
St. Maarten.—Collier et al. (2003, p.
113) reported finding two nesting
colonies on St. Maarten Island in 2001,
with a total of 64 nesting pairs, but in
2002 found no breeding pelicans at one
of the two sites surveyed in 2001.
Reasons for the lack of breeding activity
in 2002 are unknown, although Collier
et al. (2003, p. 113) suggested a
disturbance event could have been the
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cause. The May 2006 newsletter for the
Society for the Conservation and Study
of Caribbean Birds (Society for the
Conservation and Study of Caribbean
Birds 2006) notes that St. Maarten’s
proposed Important Bird Areas of Fort
Amsterdam and Pelikan Key host
regionally important populations of
nesting brown pelicans, although
numbers of nesting birds are not given.
Puerto Rico and U.S. Virgin Islands.—
Collazo et al. (1998, pp. 63–64)
compared demographic parameters
between 1980–82 and 1992–95 for
brown pelicans in Puerto Rico. The
mean number of individuals observed
during winter aerial population surveys
between 1980 and 1982 was 2,289,
while mean winter counts from 1992 to
1995 averaged only 593 birds (Collazo et
al. 1998, p. 63). Reasons for the decrease
in number of wintering birds between
the two periods are not known;
however, migrational shifts could have
contributed to the decrease in winter
counts between survey periods (Collazo
et al. 1998, p. 63). The number of nests
observed at the selected study sites did
not show such an appreciable decline
during the same period for Puerto Rico
and the nearby U.S. Virgin Islands, with
nest counts ranging from 167 to 250
during 1980 to 1982, compared with 222
and 256 during 1992 to 1993 (Collazo et
al. 1998, p. 64). Collazo et al. (2000, p.
42) estimated approximately 120–200
nesting pairs in Puerto Rico and 300–
350 nesting pairs in the U.S. Virgin
Islands. Information provided by Puerto
Rico’s Department of Natural and
Environmental Resources places
population estimates in the same
relative range as Collazo et al. (1998)
with an average of 437 individuals
found in aerial surveys conducted from
1996 to 2004 (Department of Natural
and Environmental Resources 2008, pp.
1, 3), although it is not known if these
were summer or winter surveys.
Additionally, the U.S. Virgin Islands’
Department of Planning and Natural
Resources reports that about 300 nesting
pairs have been counted in the U.S.
Virgin Islands annually (Department of
Planning and Natural Resources 2008, p.
1), a comparable number to that
reported by Collazo et al. (1998).
Finally, more recent information from
Bradley and Norton (2009, p. 275)
reports 265 breeding pairs in Puerto
Rico and 325 breeding pairs in the U.S.
Virgin Islands.
Cuba.—Acosta-Cruz and Mugica´
Valdes (2006, pp. 10, 65) reported that
brown pelicans are a common resident
species, with the population augmented
by migrants during the winter. Brown
pelicans have been documented nesting
´
at five sites in the Archipielago Sabana-
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¨
Camaguey and in the Refugio de Fauna
´
´
Rıo Maximo (Acosta-Cruz and Mugica´
Valdes 2006, pp. 32–33). The number of
´
nesting pairs at Refugio de Fauna Rıo
´
Maximo was estimated at 16 to 36 pairs
during monitoring in 2001 and 2002
´
(Acosta-Cruz and Mugica-Valdes 2006,
p. 33). No estimates were given for other
nesting sites. More recent data from
Bradley and Norton (2009, p. 275)
estimates there to be 300 nesting pairs
in 18 colonies in Cuba.
Aruba.—Information provided by
Veterinary Service of Aruba, the
country’s Convention on International
Trade in Endangered Species of Wild
Fauna and Flora (CITES; 27 U.S.T. 1087)
Management Authority, estimates the
breeding population on the island to be
20 pairs with a total population estimate
of 60 individuals (Veterinary Service of
Aruba 2008, p. 1).
Summary of West Indies.—Although
we do not have detailed information on
brown pelicans throughout all of the
islands of the West Indies, the
distribution and abundance of current
breeding colonies reported by Collazo et
al. (2000, p. 42), van Halewyn and
Norton (1984, pp. 174–175, 201), and
Bradley and Norton (2009, p. 275) are
all similar and in the range of 1,500 to
2,000 breeding pairs.
Caribbean and Atlantic Coasts of
Mexico, Central America, and South
America
No comprehensive population
estimates for the Caribbean and Atlantic
Coasts of Central and South America are
available to our knowledge, although
some estimates for other portions of the
species’ range include birds that nest on
the mainland coast or offshore islands
(e.g., van Halewyn and Norton’s
estimate of 6,200 pairs in the Caribbean
included birds nesting on the mainland
and offshore islands of Colombia and
Venezuela (1984, p. 201)).
Mexico.—Isla Contoy Reserva
Especial de la Biosfera off the coast of
Cancun, Quintana Roo, Mexico, was the
site of Mexico’s largest brown pelican
nesting colony in 1986, with 300 nesting
pairs (Blankenship 1987, p. 2). By the
spring of 1996, 700 to 1,000 pairs of
brown pelicans were estimated to be
nesting on Isla Contoy (Shields 2002, p.
35). Four other colonies in this region
accounted for 128 nesting pairs in 1986
(Blankenship 1987, p. 2).
Belize.—Miller and Miller (2006, pp.
7, 64) analyzed Christmas Bird Count
data collected in Belize from 1969–2005
and reported that brown pelican
numbers over this period have remained
about the same. References compiled
and summarized by Miller and Miller
(2006, pp. 144–149) variously report
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brown pelicans as: ‘‘Common: high
density, likely to be seen many places,’’
‘‘Transient, present briefly as migrant,’’
‘‘Resident, species present all year,’’ and
‘‘apparently secure in Belize.’’ Brown
pelicans are also reported in one
reference as nesting on several cays
(small, low islands composed largely of
coral or sand), but no information on
number of nesting birds or locations are
given.
Guatemala.—Brown pelicans in
Guatemala are considered to be a
breeding resident (Eisermann 2006, p.
55), although locations of nesting sites
and number of breeding pairs are not
given. Eisermann (2006, p. 65) estimated
the Caribbean slope population of
brown pelicans in Guatemala to consist
of approximately 376 birds.
Honduras.—Thorn et al. (2006, p. 29)
report brown pelicans nesting on the
Caribbean coast of Honduras and
offshore islands. Brown pelicans are
reported as a common resident in
Honduras, with numbers estimated to
range between 10,000 and 25,000 birds
and a stable population trend (Thorn et
al. 2006, p. 20).
Nicaragua.—Zolotoff-Pallais and
Lezama (2006, p. 74) report that the
number of brown pelicans within
Nicaragua falls within the range 1001–
5000 and is stable, although they do not
indicate whether this estimate
represents only breeding birds.
Costa Rica.—Brown pelicans are
considered a resident species in Costa
Rica, but are not reported nesting on the
Caribbean coast of Costa Rica (Quesada
2006, pp. 9, 46).
Panama.—Brown pelicans primarily
nest in the Gulf of Panama on the
Pacific coast with no nesting reported
on the Caribbean coast (Angehr 2005,
pp. 15–16). However, brown pelicans do
winter along the Caribbean coast of
Panama. In 1993, 582 brown pelicans
were counted in Panama (Shields 2002,
p. 22) along the Caribbean coast, and
Angehr (2005, p. 79) considers brown
pelicans to be a ‘‘fairly common
migrant’’ along the Caribbean coast.
Colombia.—Moreno and Buelvas
(2005, p. 57) report that brown pelicans
occur at four sites on the Caribbean
coast of Colombia, with a good
population of brown pelicans in the
coastal wetlands of La Guajira.
However, no estimate of numbers of
breeding birds was given. Information
provided by Colombia’s Instituto de
Investigaciones Marinas y Costeras
(INVEMAR) report approximately 20
breeding pairs on the Caribbean coast of
Colombia with additional migratory
birds present (INVEMAR 2008).
Venezuela.—Based on aerial surveys
of the Venezuelan coast, Guzman and
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Schreiber (1987, p. 278) estimated a
population size of 17,000 brown
pelicans in 25 colonies. Within those
breeding colonies, 3,369 nests were
counted (Guzman and Schreiber 1987,
p. 278). More recently, Rodner (2006, p.
9) confirms that there are approximately
25 brown pelican colonies in Venezuela.
Rodner (2006, p. 9) does not give an
overall estimate of the brown pelican
population in Venezuela but notes more
than 1,700 nests have been documented
in four of the largest breeding colonies,
while another recent census of four sites
resulted in counts of 2,097 pelicans.
South of Venezuela, brown pelicans
are reported as a nonbreeding migrant in
Guyana (Johnson 2006, p. 5), French
Guiana (Delelis and Pracontal 2006, p.
57), Surinam (Haverschmidt 1949, p. 77;
Ottema 2006, p. 3), and Brazil (De Luca
et al. 2006, pp. 3, 40)
Summary of the Caribbean/Atlantic
Coast.—In general, brown pelicans are
broadly distributed on the Caribbean
and Atlantic coasts of southern Mexico
and Central and South America and are
still present throughout their historic
range with population numbers likely in
the range of 30,000 to 50,000 birds,
based on the numbers presented above.
California and Pacific Coast of Northern
Mexico
The most recent population estimate
of the brown pelican subspecies that
ranges from California to Mexico along
the Pacific Coast is approximately
70,680 nesting pairs, which equates to
141,360 breeding birds (Anderson et al.
2007, p. 8). They nest in four distinct
geographic areas: (1) The Southern
California Bight (SCB), which includes
southern California and northern Baja
California, Mexico; (2) southwest Baja
California; (3) the Gulf of California,
which includes coastlines of both Baja
California and Sonora, Mexico; and (4)
mainland Mexico further south along
the Pacific coastline (including Sinaloa
and Nayarit) (Service 1983, p. 8).
During the late 1960s and early 1970s,
the SCB population declined to fewer
than 1,000 pairs and reproductive
success was nearly zero (Anderson et al.
1975, p. 807). In 2006, approximately
11,695 breeding pairs were documented
at 10 locations in the SCB: 3 locations
on Anacapa Island, 1 on Prince Island,
and 1 on Santa Barbara Island in
California; 3 on Los Coronados Islands,
1 on Islas Todos Santos, and 1 on Isla
´
San Martın in Mexico within the SCB
(Henny and Anderson 2007, p. 9; Gress
2007). In 2007, brown pelicans in
California nested on west Anacapa
Island and Santa Barbara Island but did
not nest on Prince Island (Burkett et al.
2007, p. 8). The populations on Todos
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´
Santos and San Martın islands were
previously extirpated in 1923 and 1974,
respectively; however, these were
recently found to be occupied (Gress et
al. 2005, pp. 20–25). Todos Santos
Island had about 65 nests in 2004, but
there were no nests in 2005. This colony
is currently considered to be ephemeral,
occurring some years and then not
others (Gress et al. 2005, p. 28). At San
´
Martın Island, 35 pairs were reported in
1999, a small colony was noted in 2000,
and 125–200 pairs were seen in 2002,
2003, and 2004 (Gress et al. 2005, pp.
20–25).
The southwest Baja California coastal
population has about 3,100 breeding
pairs, the Gulf of California population
is estimated at 43,350 breeding pairs,
and the mainland Mexico populations
(including islands) is estimated to have
12,385 breeding pairs (Anderson et al.
2007, p. 8). The Gulf of California
population remained essentially the
same from 1970 to 1988 (Everett and
Anderson 1991, p. 125). It is thought
that populations in Mexico have been
stable since the early 1970s (when longterm studies began) because of their
lower exposure to organochlorine
pesticides (e.g., DDT), although annual
numbers at individual colonies fluctuate
widely due to prey availability and
human disturbance at colonies (Everett
and Anderson 1991, p. 133).
Summary of California and Pacific
Coast of Northern Mexico.—Henny and
Anderson (2007, pp. 1, 8) concluded
that their preliminary estimates of
nesting pairs in 2006 suggest a large and
healthy total breeding population for
California and the Pacific coast of
Mexico.
Pacific Coast of Central America and
South America
As with the Caribbean and Atlantic
coasts of Central and South America,
there are no comprehensive population
estimates for brown pelicans along this
portion of their range.
Guatemala, El Salvador, Honduras,
and Nicaragua.—Brown pelicans are
considered a nonbreeding visitor on the
Pacific slope of Guatemala (Eisermann
2006, p. 4) with an estimated abundance
of 2,118 birds. About 800 brown
pelicans are widely distributed along
the Pacific Coast of El Salvador (Ibarra
Portillo 2006, p. 2). However, Herrera et
al. (2006, p. 44) reported brown pelicans
to be a nonbreeding visitor in El
Salvador with numbers falling within
the range 1,001–10,000 and an
increasing trend. Brown pelicans occur
on the Pacific Coast of Honduras but are
not reported to nest there (Thorn et al.
2006, p. 26, 29). Zolotoff-Pallais and
Lezama (2006, p. 74) report that the
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number of brown pelicans within
Nicaragua falls within the range 1,001–
5,000, but do not indicate locations or
breeding status.
Costa Rica.—The Costa Rican
Ministry for Environment and Energy
has reported that several breeding
colonies exist on the Pacific Coast from
the Nicaraguan border to the Gulf of
Nicoya and include the islands of
Bolanos and Guayabo (Service 2007a, p.
13). Shields (2002, p. 35) estimated as
many as 850 pairs in Costa Rica.
However, Quesada (2006, p. 37)
estimated the brown pelican population
in Costa Rica to fall within the range
10,000–25,000 birds with a stable
population trend.
Panama.—Estimates of brown
pelicans in Panama have varied greatly
over the years. In 1981, Batista and
Montgomery (1982, p. 70) estimated that
25,500 adults and chicks were known to
occur on just the Pearl Island
Archipelago in the Gulf of Panama. In
1982, Montgomery and Murcia (1982, p.
69) estimated 70,000 adults occurred at
7 colonies within the Gulf of Panama.
By 1988, 6,031 brown pelicans were
known from just the Gulf, while in
1998, only 3,017 brown pelicans were
thought to occur along the entire Pacific
Coast of Panama, including the Gulf
(Shields 2002, p. 22). By 2005, 4,877
brown pelican nests were reported just
in the Gulf of Panama and a total
population was estimated to be about
15,000 individuals for the entire Pacific
Coast of Panama, which includes 150
nests found at Coiba Island in 1976
(Angehr 2005, p. 6). Angehr (2005, p.
12) also reported that those individual
colonies that had been studied
experienced an overall increase of 70
percent in nest numbers from 1979 to
2005, and describes the brown pelican
on the Pacific Coast of Panama as an
‘‘abundant breeder.’’
Colombia.—Moreno and Buelvas
(2005, p. 57) list brown pelicans as
occurring at three protected sites on the
Pacific coast of Colombia: Malpelo
Island, Gorgona Island, and Sanquianga.
Naranjo et al. (2006b, p. 178) estimated
2,000–4,000 brown pelicans at
Sanquianga on the mainland and 4,800–
5,200 on Gorgona Island. Brown
pelicans were considered to be one of
the most abundant resident species in a
1996–1998 assessment of waterbird
populations on the Pacific Coast of
Colombia (Naranjo et al. 2006a, p. 181).
Naranjo et al. (2006b, p. 179) concluded
that preliminary results of their
waterbird monitoring program on the
Pacific coast of Colombia indicate that
populations of Pelecaniformes (which
include brown pelicans) in the three
protected areas are stable. INVEMAR
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(2008) also report approximately 3,000
breeding pairs known from the Pacific
coast of Colombia, which represents
approximately 6,000 birds and is
consistent with estimates by Naranjo et
al. (2006b).
Ecuador.—On Ecuador’s Galapagos
Islands, Shields (2002, p. 35) cites
reports of a few thousand pairs. Delaney
and Scott (2002, p. 29) estimated the
population on the Galapagos to be 5,000
birds. Santander et al. (2006, pp. 44, 49)
reported that brown pelicans in the
Galapagos number less than 10,000 and
are considered common there, while
populations on the mainland range from
25,000 to 100,000. The Ministerio del
Ambiente of Ecuador has reported that
nesting brown pelicans are widely
distributed and fairly common along the
mainland coast of that country (Rojas
2006).
Peru.—Shields (2002, p. 22)
summarizes estimates of brown pelicans
in Peru at 420,000 adults in 1981–1982,
110,000 in 1982–1983, 620,000 in 1985–
1986, and 400,000 in 1996. Franke
(2006, p. 10) reported that a 1997 survey
of guano birds counted 140,000 brown
pelicans with an increasing population
trend reported; however, it is unclear
from the report whether that number
represents a total estimate of the brown
pelican population in Peru or a subset
of birds nesting on islands managed for
guano production.
Chile.—The range of brown pelicans
in Chile extends from the extreme
´
northern city of Arica (Rodrıguez 2006)
to occasionally as far south as Isla
´
Chiloe (Aves de Chile 2006, p. 1). The
total population size for Chile is
unknown (Shields 2002, p. 35). The
´
˜
breeding population on Isla Pajaro Nino
in central Chile was 2,699 pairs in
1995–1996, 1,032 pairs in 1996–1997,
˜
and none during the 1997–1998 El Nino
(a temporary oscillation of the oceanatmosphere system) year (Simeone and
Bernal 2000, p. 453).
Two sightings of brown pelicans in
Argentina in 1993 and 1999 are
considered ‘‘hypothetical’’ records
because they are not documented by
specimens, photographs, or other
concrete evidence (Lichtschein 2006).
Summary of Pacific Coast of Central
and South America.—Brown pelicans
are abundant breeders along the Pacific
coast of Central and South America with
population numbers in the range of
65,000 to 200,000 birds, not including
an estimated 400,000 birds in Peru.
Summary—Global Distribution and
Population Estimates
As discussed above, currently listed
brown pelican populations are widely
distributed throughout the coast of the
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Gulf of Mexico from Mississippi to
Texas and the coast of Mexico; along the
Caribbean coast from Mexico south to
Venezuela; along the Pacific Coast from
British Columbia, Canada, south
through Mexico into Central and South
America; and in the West Indies.
Population estimates for various States,
regions, and countries reviewed above
are not strictly comparable because they
were not made using any standard
protocol or methodology, and in many
cases the process by which the estimates
were developed is not described. For
example, surveys conducted in different
parts of the year may yield differing
results due to migratory trends and
breeding patterns. While in some cases
these estimates may be reliable in
describing local abundance and trends,
because of their incomparability, they
have limited value in estimating
absolute size or trends in the global
population.
During our 5-year status review of the
brown pelican, we estimated the global
listed brown pelican population based
on the best available information at the
time of the review, which included most
but not all of the individual estimates
given above. Although these estimates
represented the best available
information at the time of the review,
because of the lack of standardization
and major differences in determining
population estimates, we used
conservative assumptions in tabulating
these data in order to make a
conservative estimate of the global
population size of the brown pelican
(see Service 2007a, pp. 43–45 and 60–
62). Specifically, where only numbers of
nests are known, the total number of
nests was simply doubled to obtain an
estimate of total population size for an
area. This method likely underestimates
the population size because there are
likely to be unpaired or immature
nonbreeders in the population.
Additionally, where a population
estimate found in the literature was a
range of numbers, the lower number
was used in calculating the global
estimate. Population size is merely one
factor in determining whether a species
is recovered, and this approach assures
we are making our determination in a
manner that is protective of the species.
This total, or global estimate, as given
in our 5-year review, is for the listed
brown pelican, which does not include
the Atlantic coast of the United States,
Florida, and Alabama. The total based
on regional estimates is over 620,000
individuals, which includes an
estimated 400,000 pelicans from Peru
(Service 2007a, pp. 43–45 and 60–62).
This is likely a conservative estimate
given that estimates for some countries
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given above (for example, estimates for
Colombia and Cuba) were not readily
available at the time we conducted our
5-year review. Other recent estimates
yield similar numbers. Kushlan et al.’s
(2002, p. 64) estimate for the North
American Waterbird Conservation Plan
area, which includes Canada, the United
States, Mexico, Central America, the
Caribbean, and Caribbean islands of
Venezuela, was 191,600–193,700
breeders. Delaney and Scott (2002, p.
29) applied a correction factor to
Kushlan et al.’s estimate to account for
immature birds and nonbreeders to
estimate a population of 290,000 birds.
Neither estimate includes birds on the
Pacific Coast of South America. Delaney
and Scott (2002, p. 29) additionally
estimated the brown pelican population
on the Galapagos to be about 5,000
birds, and the population on the Pacific
Coast of South America (estimate is for
the subspecies Pelecanus occidentalis
thagus, found in Peru and Chile) to
range from 100,000–1,000,000 birds.
Shields’ (2002, p. 21) population
estimate of 202,600–209,000 brown
pelicans also did not include the
Peruvian subspecies. While each of
these estimates covers slightly different
areas, they are all in general agreement
and indicate that the listed population
of brown pelicans, excluding the
Peruvian subspecies, totals 200,000 or
more individuals, while the Peruvian
subspecies numbers in the few hundred
thousand.
Recovery Plan
Section 4(f) of the Act directs us to
develop and implement recovery plans
for listed species. While brown pelicans
were listed throughout their range,
recovery planning efforts for the brown
pelican focused primarily on those
portions of the species’ range within the
United States. We have published three
recovery plans for the brown pelican: (1)
Recovery Plan for the Eastern Brown
Pelican (Service 1979); (2) the California
Brown Pelican Recovery Plan (Service
1983); and (3) Recovery Plan for the
Brown Pelican in Puerto Rico and the
U.S. Virgin Islands (Service 1986).
Section 4(f) of the Act requires the
Service to develop and implement
recovery plans for the conservation and
survival of threatened and endangered
species, unless we find that such a plan
will not promote the conservation of the
species. The Act directs that, to the
maximum extent practicable, we
incorporate into each plan: (1) Sitespecific management actions that may
be necessary to achieve the plan’s goals
for conservation and survival of the
species; (2) objective, measurable
criteria, which when met would result
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in a determination, in accordance with
the provisions of section 4 of the Act,
that the species be removed from the
list; and (3) estimates of the time
required and cost to carry out the plan.
However, revisions to the List (adding,
removing, or reclassifying a species)
must reflect determinations made in
accordance with section 4(a)(1) and 4(b).
Section 4(a)(1) requires that the
Secretary determine whether a species
is threatened or endangered (or not)
because of one or more of five threat
factors. Therefore, recovery criteria must
indicate when a species is no longer
threatened or endangered by any of the
five factors. In other words, objective,
measurable criteria, or recovery criteria,
contained in recovery plans must
indicate when an analysis of the five
threat factors under 4(a)(1) would result
in a determination that a species is no
longer threatened or endangered.
Section 4(b) requires the determination
made under section 4(a)(1) as to
whether a species is threatened or
endangered because of one or more of
the five factors be based on the best
available science.
Thus, while recovery plans are
intended to provide guidance to the
Service, States, and other partners on
methods of minimizing threats to listed
species and on criteria that may be used
to determine when recovery is achieved,
they are not regulatory documents and
cannot substitute for the determinations
and promulgation of regulation required
under section 4(a)(1). Determinations to
remove a species from the list made
under section 4(a)(1) must be based on
the best scientific and commercial data
available at the time of the
determination, regardless of whether
that information differs from the
recovery plan.
In the course of implementing
conservation actions for a species, new
information is often gained that requires
recovery efforts to be modified
accordingly. There are many paths to
accomplishing recovery of a species,
and recovery may be achieved without
all criteria being fully met For example,
one or more criteria may have been
exceeded while other criteria may not
have been accomplished, yet the Service
may judge that, overall, the threats have
been minimized sufficiently, and the
species is robust enough, to reclassify
the species from endangered to
threatened or perhaps delist the species.
In other cases, recovery opportunities
may have been recognized that were not
known at the time the recovery plan was
finalized. These opportunities may be
used instead of methods identified in
the recovery plan.
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59449
Likewise, information on the species
may be learned that was not known at
the time the recovery plan was
finalized. The new information may
change the extent that criteria need to be
met for recognizing recovery of the
species. Overall, recovery of species is
a dynamic process requiring adaptive
management, planning, implementing,
and evaluating the degree of recovery of
a species that may, or may not, fully
follow the guidance provided in a
recovery plan.
Thus, while the recovery plan
provides important guidance on the
direction and strategy for recovery, and
indicates when a rulemaking process
may be initiated, the determination to
remove a species from the List is
ultimately based on an analysis of
whether a species is no longer
threatened or endangered. The
following discussion provides a brief
review of recovery planning for the
brown pelican, as well as an analysis of
the recovery criteria and goals as they
relate to evaluating the status of the
species.
The Recovery Plan for the Eastern
Brown Pelican, which includes the
Atlantic and Gulf Coasts of the United
States, does not identify recovery
criteria because the causes of the
species’ decline were not well
understood at the time the plan was
prepared. The recovery team viewed the
wide distribution of the species, rather
than absolute numbers, as the species’
major strength against extinction
(Service 1979, p. iv). This recovery plan
also addressed brown pelicans in
Alabama, Florida, and the Atlantic
Coast of the United States, but because
these populations have already been
delisted, we only discuss the plan’s
objectives for the portion of the range
that remained listed in Louisiana and
Texas.
The recovery plan states a general
objective to reestablish brown pelicans
on all historically used nesting sites in
Louisiana and Texas (Service 1979, p.
iii). The plan identified 9 sites in
Louisiana and 11 sites in Texas. These
included historic, current (at the time of
the recovery plan), and restored islands.
Since 2005, brown pelicans have nested
at between 11 and 15 sites in Louisiana
and at 12 sites in Texas (Hess and
Linscombe 2006, pp. 1–4, 7–8; Service
2006, p. 2). These sites include some of
the same sites identified in the recovery
plan as well as previously unknown or
newly colonized sites.
The number and location of nesting
sites has varied from year to year along
the Gulf Coast due in part to frequent
tropical storms, but generally meet the
recovery plan goals for number of
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nesting sites. The northern Gulf of
Mexico coast is subject to frequent
severe tropical storms and hurricanes,
which can cause significant changes to
brown pelican nesting habitat. Past
storms have resulted in changes to or
loss of historical nesting sites, but
brown pelicans seem well adapted to
responding to losses of breeding sites by
moving to new locations (Hess and
Durham 2002, p. 7; Wilkinson et al.
1994, p. 425; Williams and Martin 1968,
p. 136), and the species has clearly
shown its ability to rebound (Williams
and Martin 1968, p. 130; Holm et al.
2003, p. 432; Hess and Linscombe 2006,
pp. 5, 13) (see ‘‘Storm effects, weather,
and erosion impacts to habitat’’ under
Factor A for further discussion).
While nesting is not occurring on all
historically identified sites in Texas and
Louisiana, the number of currently used
nesting sites meets or exceeds the
numbers identified in the recovery plan
and supports sustainable populations of
brown pelicans. Because brown pelicans
have demonstrated the ability to move
to new breeding locations when a
nesting island is no longer suitable,
meeting the exact number and location
of nesting sites in Texas and Louisiana
identified in the recovery plan is not
necessary to achieve recovery for the
brown pelican. As discussed further
below, we also have considered the
population’s wide distribution,
numbers, and productivity as indicators
that the threats have been reduced such
that the population is recovered and
sustainable.
The Recovery Plan for the Brown
Pelican in Puerto Rico and the U.S.
Virgin Islands has delisting criteria
solely for the area covered by the plan.
The criteria are to maintain a 5-year
observed mean level of: (1) 2,300
individuals during winter, and (2) 350
breeding pairs at the peak of the
breeding season. Both recovery criteria
are solely based on demographic
characteristics and do not provide an
explicit reference point for determining
whether threats have been reduced. The
levels in the criteria were based on
studies of brown pelicans from 1980 to
1983 (Collazo 1985). Subsequent winter
counts from 1992 to 1995 in Puerto Rico
were 74 percent lower than during
1980–1982 (593 individuals compared
to 2,289). Although the 1992 to 1995
counts did not include the Virgin
Islands, it appears likely that the first
criterion had not been met as of 1995
(Collazo et al. 1998). However, reasons
for lower counts are unknown. Collazo
et al. (1998, pp. 63–64) concluded that
habitat was not limiting and suggested
that migrational shifts could have
contributed to the decrease in numbers
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and that longer term monitoring of at
least 6 to 8 years is needed to define an
acceptable range of population
parameters for brown pelicans in the
Caribbean. Collazo et al. (1998, p. 64)
also concluded that contaminants are
not affecting brown pelican
reproduction.
Thus, while the first criterion, based
on 4 years of data, may not be sufficient
to establish a realistic figure to reflect
recovery, it also does not address
whether threats to the species are still
present. Also, because the criterion
applies to only a small portion of the
species’ range, as well as only a portion
of the species’ range in the Caribbean,
we do not consider it relevant for
determining whether the brown pelican
is recovered globally. Of the two
recovery criteria, the second criterion is
the more appropriate to the evaluation
of the status of the species as it reflects
population productivity. The number of
pairs seemed to be holding steady
between the early 1980s and the 1990s
with estimates given by Collazo et al.
(2000, p. 42) of 165 pairs for Puerto Rico
and 305–345 pairs for the U.S. Virgin
Islands. While this estimate is not a
5-year observed mean, the estimated
number is consistent with the recovery
criterion for number of breeding pairs.
Moreover, data from the U.S. Virgin
Islands (Department of Planning and
Natural Resources 2008, p. 1) supports
the Collazo et al. (2000, p. 42) numbers
by estimating the brown pelican
population there at about 300 breeding
pairs.
The California Brown Pelican
Recovery Plan only covers the California
brown pelican subspecies (P. o.
californicus), which includes the Pacific
Coast of California and Mexico,
including the Gulf of California. The
primary objective of this recovery plan
is to restore and maintain stable, selfsustaining populations throughout this
portion of the species’ range. To
accomplish this objective, the recovery
plan calls for: (1) Maintaining existing
populations in Mexico; (2) assuring
long-term protection of adequate food
supplies and essential nesting, roosting,
and offshore habitat throughout the
subspecies’ range; and (3) restoring
population size and productivity to selfsustaining levels in the SCB at both the
Anacapa and Los Coronados Island
colonies. Existing populations appear to
be stable in Mexico and throughout the
subspecies range (Everett and Anderson
1991, p. 133; Henny and Anderson
2007, pp. 1, 8), food supplies are
assured by the Coastal Pelagic Species
Fishery Management Plan, and the
majority of essential nesting and
roosting habitat throughout the
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subspecies’ range is protected (see
‘‘Summary of Factors Affecting the
Species’’ below for further discussion).
Therefore, criteria 1 and 2 of the
recovery plan have been met.
For population and productivity
objectives, the recovery plan included
the following additional criterion: (a)
When any 5-year mean productivity for
the SCB population reaches at least 0.7
young per nesting attempt from a
breeding population of at least 3,000
pairs, the subspecies should be
considered for reclassification from
endangered status to threatened status;
and (b) When any 5-year mean
productivity for the SCB population
reaches at least 0.9 young per nesting
attempt from a breeding population of at
least 3,000 pairs, the subspecies should
be considered for delisting.
Consideration for reclassification to
threatened would require a total
production averaging at least 2,100
fledglings per year over any 5-year
period. Consideration for delisting
would require a total production
averaging at least 2,700 fledglings per
year over any 5-year period.
The criterion, including both
productivity and population size, for
downlisting to threatened has been met
at least 10 times since 1985. The
delisting population criterion of at least
3,000 breeding pairs has been exceeded
every year since 1985, with the
exception of 1990 and 1992, which saw
only 2,825 and 1,752 pairs, respectively.
In most years, the nesting population far
exceeds the 3,000 pair delisting goal; it
has exceeded 6,000 pairs for 10 of the
last 15 years (Gress 2005). Additionally,
the delisting criterion of at least 2,700
fledglings per year over any 5-year
period has been met at least 11 times
since 1985 (Gress 2005). However,
although productivity has improved
greatly since the time of listing, the
productivity criterion for delisting has
not been met and the SCB population
consistently has low productivity, with
a mean of 0.63 young fledged per
nesting attempt from 1985 to 2005
(Gress and Harvey 2004, p. 20; Gress
2005).
Productivity is an important
parameter used for evaluating
population health; however, it is
difficult to determine an objective and
appropriate minimum value. The 0.9
young per nesting attempt given in the
recovery plan was the best estimate
based on a review of brown pelican
reproductive parameters in Florida and
the Gulf of California (Schreiber 1979,
p. 1; Anderson and Gress 1983, p. 84),
because pre-DDT productivity for the
SCB population was unknown. Despite
the fact that this goal has not been
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reached, reproduction has been
sufficient to maintain a stable
population for more than 20 years. Most
colonies expanded during this interval,
including the long-term colonization of
Santa Barbara Island, which suggests
that productivity has been sufficient to
maintain a stable-to-increasing
population. In conclusion, the first two
recovery criteria for the California
Brown Pelican Recovery Plan have been
met. As discussed above, the population
component of the third criterion has
been far exceeded, while the
productivity component has not been
met. We have concluded, based on
current population size and
productivity, that the productivity
component of the third criterion is no
longer appropriate because current
productivity is sufficient to maintain a
viable population of brown pelicans.
Please see responses to comments 6 and
8 below for additional discussion of the
productivity criterion.
Recovery Planning Summary—The
three recovery plans for the brown
pelican discussed above have not been
actively used in recent years to guide
recovery of the brown pelican because
they are either outdated, lack recovery
criteria for the entire species, or in the
case of the eastern brown pelican, lack
recovery criteria altogether. No
subsequent revisions have been made to
any of these original recovery plans. No
single recovery plan covers the entire
range of the species in the United States,
and the remainder of the range outside
the United States, including Central
America, South America, and most of
the West Indies is not covered by a
recovery plan. Additionally, the
recovery criteria in these plans do not
specifically address the five threat
factors used for listing, reclassifying, or
delisting a species as outlined in section
4(a)(1) of the Act. Consequently, the
recovery plans do not provide an
explicit reference point for determining
the appropriate legal status of the brown
pelican based either on alleviating the
specific factors that resulted in its initial
listing as an endangered species or on
addressing new risk factors that may
have emerged since listing. As noted
above, recovery is a dynamic process
and analyzing the degree of recovery
requires an adaptive process that
includes not only evaluating recovery
goals and criteria but also new
information that has become available.
Thus, while some recovery criteria and
many of the goals in the three brown
pelican recovery plans have been met,
our evaluation of the status of the brown
pelican in this rule is based largely on
the analysis of threats in our recently
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completed 5-year review (Service 2007a,
pp. 1–66), available at https://
ecos.fws.gov/docs/five_year_review/
doc1039.pdf, and presented below.
Summary of Public and Peer Review
Comments and Recommendations
In our February 20, 2008 proposed
rule, we requested all interested parties
submit information, data, and comments
concerning multiple aspects of the
status of the brown pelican. The
comment period was open from
February 20, 2008, through April 21,
2008.
In accordance with our policy on peer
review, published on July 1, 1994 (59
FR 34270), we solicited opinions from
eight expert scientists who are familiar
with this species regarding pertinent
scientific data and assumptions relating
to supportive biological and ecological
information for the proposed rule.
Reviewers were asked to review the
proposed rule and the supporting data,
to point out any mistakes in our data or
analysis, and to identify any relevant
data that we might have overlooked.
Four of the eight peer reviewers
submitted comments. Three of those
four were generally supportive of the
proposal to remove the brown pelican
from the Federal List of Threatened and
Endangered Species while the fourth
reviewer did not offer an opinion. Their
comments are included in the summary
below and/or incorporated directly into
this final rule.
During the 60-day comment period,
we received comments from 19
individuals, organizations, and
government agencies. We have read and
considered all comments received. We
updated the rule where it was
appropriate, and we responded to all
substantive issues received, below.
Peer Review Comments
(1) Comment: The inclusion of brown
pelicans on the List (Federal List of
Threatened and Endangered Wildlife)
has provided us with a means of
protecting habitat that has also
protected many other species that share
the marine habitat with the brown
pelican. With this delisting, we will lose
protections afforded to all these other
marine species.
Response: When making listing and
delisting determinations, we are only to
consider the best scientific and
commercial information data in
preparing the five-factor analysis. This
analysis has us consider a variety of
impacts to the species in question and
the regulatory mechanisms that may
mitigate those impacts, but does not
allow us to consider impacts of listing
and delisting on other species. However,
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brown pelicans will remain protected by
the Migratory Bird Treaty Act of 1918
(16 U.S.C. 703–711; 40 Stat. 755) and, as
discussed below, numerous other
mechanisms confer protections to the
brown pelican and to other species and
habitats that are not dependent on the
protections afforded brown pelicans by
the Endangered Species Act.
(2) Comment: Multiple commenters
expressed concerns over our global
population estimate, specifically noting
that the number reached is vague and
speculative because a complete and
coordinated survey for the entire species
has never been done. Reviewers
requested use of additional information
if possible and, if not possible, inclusion
of a more thorough justification for
relying on the old and widely varying
data in our global population estimate.
Response: The Act directs that we use
the best scientific and commercial data
available in making our determinations.
This rulemaking was initially prompted
by a petition to delist the species (see
the ‘‘Previous Federal Actions’’ section
of our proposed rule (February 20, 2008;
73 FR 9408)). In order to fulfill our
requirements to respond to the petition
and complete the rulemaking process
once begun, we are statutorily required
to make a determination at this time
based on the best scientific and
commercial data currently available to
us. We recognize that additional
research and coordinated efforts would
yield a more reliable and accurate global
population estimate. We have used the
best available scientific and commercial
data in developing our global
population estimate. However, we have
not relied solely upon this estimate in
making our determination that the
brown pelican no longer warrants
listing. This number is developed and
presented in efforts to provide the
reader a general estimate of the scale of
the global population, allow
comparisons with other available
estimates, and provide a summary and
conclusion of the various estimates
provided. While the accuracy of the
specific number cannot be determined
due to differences in survey
methodology and information quality,
the relative scale of the number, in the
hundreds of thousands, is useful in
demonstrating the degree of recovery
the species has acheived and the
absence of significant threats to the
species. We have expanded the
discussion under the ‘‘Summary—
Global Population Estimate’’ section to
further explain our rationale in
developing this estimate.
(3) Comment: The discussion of the
significance of the Puerto Rico brown
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pelicans makes it seem that the Service
is saying these birds are not important.
Response: In evaluating the brown
pelican and whether it continues to
require regulatory protection under the
Act, we have looked at the species from
a range-wide perspective first. The
species’ population numbers have
rebounded and threats have been
removed or reduced to the point that
protection under the Act is no longer
needed range wide. Next, we assessed
whether any population may be
experiencing localized threats over a
significant portion of the range of the
pelican such that its loss would lead to
the species as a whole being at a greater
risk of extinction. As discussed in
‘‘Significant Portion of the Range’’
section below, we have determined that
the Puerto Rico population does not
warrant listing as a significant portion of
the range of the species, although this
analysis does not imply that any
subspecies, population, or
subpopulation of brown pelican is not
important to the long-term conservation
of the brown pelican. In addition, once
the pelican is delisted, brown pelicans
will remain protected by the Migratory
Bird Treaty Act and numerous other
mechanisms, as discussed below. We
will continue working with the Puerto
Rico Department of Natural Resources
through the post-delisting monitoring
process to monitor the status of the
brown pelican in Puerto Rico.
(4) Comment: A complete study of the
genetics of the entire species would
seem to be strongly warranted in order
to further elucidate unique, small
breeding populations.
Response: We agree and encourage
continued research on the brown
pelican; however, we don’t believe a full
understanding of the genetics of each
individual breeding population is
required in order to make our delisting
decision, especially in the face of
decreased threats and increased
conservation and management
opportunities.
(5) Comment: While population
numbers confirm that delisting is the
correct action, threats to the brown
pelican still remain. There needs to be
monitoring of the brown pelican and the
marine environment post-delisting.
Response: Under section 4(g)(1) of the
Act, we are required to monitor all
species that have been recovered and
delisted for at least 5 years postdelisting. On September 30, 2009 (74 FR
50236), we announced the availability
of a draft post-delisting monitoring plan
for the brown pelican which we expect
to finalize within a year. We do not
anticipate any of the factors currently
affecting the brown pelican to become a
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threat to the status of the species in the
future; however, if at any time during
the monitoring program, data indicate
that the protective status under the Act
should be reinstated, we can initiate
listing procedures, including, if
appropriate, emergency listing.
(6) Comment: A peer reviewer noted
that the productivity criterion
developed in the California Brown
Pelican Recovery Plan was somewhat
subjective and based on comparisons to
brown pelican productivity elsewhere.
Despite this problem, the peer reviewer
notes that the overall conclusions
reached in the proposed rule concerning
these productivity criteria—that a
significant recovery has occurred in the
Southern California Bight—are
reasonable and logical.
Response: While recovery planning
and the recovery criteria often included
in recovery plans provide useful
tangible benchmarks for the planning of
conservation, the Act requires us to base
listing and delisting assessments on the
status of the species and an analysis of
the factors affecting the species. This
process allows us to determine that a
species has achieved recovery even if it
has not met all of its recovery criteria.
In this case, the significant recovery of
the California populations of brown
pelican in terms of population trends
and total population numbers has been
deemed indicative of recovery of the
species, although the specific
productivity goal has not been met.
Please see the ‘‘Recovery Plan’’ section
above for additional discussion.
(7) Comment: Multiple commenters
requested the Service to consider
various updates to the Act, the Act’s
implementing regulations, and the
recovery planning process. A peer
reviewer specifically indicated that the
Act has become ‘‘out-of-step’’ with
principles that have more recently
emerged from the fields of wildlife
management and conservation biology.
Response: While we appreciate input
on the efficacy of our program, these
comments are not relevant to this
rulemaking for the brown pelican.
Public Comments
(8) Comment: Concerning the
California brown pelican Recovery Plan,
a mean productivity value of 0.63 seems
low. Perhaps better clarification should
be made regarding the productivity
value of similar birds and how 0.63
compares.
Response: Comparisons of
productivity between species can be
very tenuous. A large number of factors
affect differences in productivity
between species and even populations
of the same species, including relative
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size of the animals, quality of the
habitat, access to resources, breeding
strategy, and feeding type.
Conceptually, in order to maintain a
population at a stable level, a
productivity value of 2.0 (2 successful
fledglings per nest) would be needed in
order to keep a population level steady,
assuming all fledglings survive to
breeding age and each pair only
reproduces once. In other words, this
scenario would result in one-to-one
replacement of adults by the new
generation. Brown pelicans breed
multiple times throughout relatively
long lifetimes, thus they have multiple
chances to replace themselves, making
numbers near and even below 1.0
acceptable. The key point in our
assessment is that the California
populations have expanded and
stabilized despite a productivity number
below the target set in our 1983
California Brown Pelican Recovery Plan
(Service 1983).
(9) Comment: The rule should include
a discussion of potential weather-related
issues caused by global warming
including hurricane frequency and
potential impacts to food supply.
Response: The Intergovernmental
Panel on Climate Change (IPCC)
concluded that warming of the climate
system is unequivocal (IPCC 2007a, p.
30). Numerous long-term changes have
been observed including changes in
arctic temperatures and ice, widespread
changes in precipitation amounts, ocean
salinity, wind patterns and aspects of
extreme weather including droughts,
heavy precipitation, heat waves and the
intensity of tropical cyclones (IPCC
2007b, p. 7). While continued change is
certain, the magnitude and rate of
change is unknown in many cases.
Tropical storms (including
hurricanes) have become more intense
over the period of record (U.S. Climate
Change Science Program (CCSP) 2008,
p. 5). Multiple studies and analyses
have been done concerning how tropical
storm activity may change in the future.
Predicting change in frequency and
intensity is quite complicated with
some factors potentially negating or
exacerbating each other (e.g., sea surface
temperature versus vertical wind shear,
a measure of the difference in wind
speed and duration over a vertical
distance). There is general agreement
that, based on current information, the
intensity of individual storms is likely
to increase over time; however, the
global frequency of tropical storms is
believed to stay stable or even decrease
(CCSP 2008, p. 112). Some authors show
an increase in global frequency of
tropical storms (CCSP 2008, p. 112), but
the likely magnitude and rate of those
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predicted increases is not known. Aside
from the global predictions, there is
some information that suggests the
frequency of intense tropical storms in
the North Atlantic may increase due to
atmospheric moisture and increased sea
surface temperatures; other studies
show decreased frequency due to effects
of wind shear.
At this time, the best available
information does not allow us to predict
whether a decrease in brown pelican
populations would result from or be
correlated with a future increase in
hurricane activity. If this information
should change in the future, the postdelisting monitoring program will
reflect these declines and the situation
may be reassessed in the future.
The distribution and abundance of
marine fish species is dependent on a
variety of factors that may be influenced
by climate change including nutrient
availability, ocean currents, and water
temperature. It has been shown that
population levels of anchovies, a main
food source of pelicans in some areas,
decrease in portions of the Pacific
Ocean in response to the warmer waters
˜
found in El Nino years. Thus, it is
possible that increased ocean
temperatures, which may result from
climate change, could decrease food
supplies for brown pelicans. However,
˜
other studies show that El Nino results
in increased population levels of
sardines, another brown pelican prey
species (Chaves et al. 2003, p. 217). In
fact, multiple authors have shown that
when anchovy abundances are high,
sardine abundances are low and vice
versa (Tourre et al. 2007, p. 4).
Because the brown pelican is a
generalist in terms of prey sources, it is
able to adapt to available food sources.
Additionally, global fish populations are
likely to be affected by climate change
in much more complex ways than by
simple ocean temperature rise,
particularly the potential for shifting
ocean currents and locations of nutrient
upwelling. The response of ocean
currents to global climate change is not
well understood at this time due to the
complicating factors of natural climate
variability that occurs on various spatiotemporal scales, including the quasibiennial (2- to 3-year periods), the interannual (3- to 7-year periods), the quasidecadal (8- to 13-year periods), and the
inter-decadal (17- to 23-year periods)
(Tourre et al. 2007, p. 1), thus the
response of marine fish species and
effects to brown pelicans is even less
predictable. At this time, we are not able
to predict a decrease in brown pelican
population levels in response to food
availability effects of global climate
change.
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(10) Comment: The rule should
include an expanded discussion on
avian flu and other avian diseases.
Response: Discussion of multiple
diseases and potential effects to brown
pelicans can be found in the ‘‘Disease
and Predation’’ section below. We have
updated this section to include a
discussion of avian influenza, also
known as bird flu.
(11) Comment: Multiple commenters
indicated that a variety of issues (e.g.,
avian botulism, domoic acid poisoning,
avian disease, oil spills, mortality from
recreational fisheries, coastal
development) could be threatening the
species throughout some portion of the
range or are a greater threat to the brown
pelican than we have presented in our
analysis without providing additional
information, references, or insight to
explain their rationale.
Response: We believe we have used
the best available scientific and
commercial data in developing our fivefactor analysis. An important point to
consider when evaluating the status of
a wide-ranging species such as the
brown pelican is the scope, or the
geographic and temporal extent, of the
threat affecting the species. Some
threats adversely impact one or more
individuals of a species, while a threat
to the species would be considered a
factor that results in a decline in one or
more population parameters. There are
a lot of factors that have effects to
individuals and local populations;
however, these factors are not leading to
population level impacts and certainly
not resulting in rangewide adverse
impacts.
(12) Comment: The Puerto Rican,
West Indies, eastern Caribbean, and
Colombian populations of brown
pelican should remain listed because
threats still persist in these areas.
Response: We acknowledge that a
variety of factors continue to impact
brown pelicans in various portions of
the range of the species; however, we
did not find that these factors are
endangering the species throughout all
or a significant portion of the range of
the species now or in the foreseeable
future. Please see additional discussion
in the ‘‘Significant Portion of the Range’’
section below.
(13) Comment: The brown pelican
continues to be threatened by pesticides
because pesticides not registered for use
in the United States are readily available
for use in areas outside the United
States.
Response: It is true that the number
and kinds of pesticides available and
registered for use varies from country to
country. However, we have no
information indicating that pesticide
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use is adversely impacting the brown
pelican throughout all or a significant
portion of the range of the species. In
order to find pesticide use to be a threat
to the brown pelican we would have to
have information available that shows
that pesticides are actually being used
and are being used in a manner that
impacts the species. It would be
speculative to assert that pesticide use
is a threat to the brown pelican solely
because pesticides are accessible in
some areas. In addition, we have
determined that pesticides known to
have affected brown pelican
populations in the past are no longer a
threat to the species. Please see the
‘‘Pesticides and Contaminants’’ section
below.
(14) Comment: Additional discussion
concerning the monitoring and
enforcement of the Stockholm
Convention is needed.
Response: The Stockholm Convention
on Persistent Organic Pollutants is an
international treaty that aims to
eliminate the use of persistent organic
pollutants (e.g., DDT) globally. The
Convention went into effect on May 17,
2004, and carries the force of
international law. Monitoring of
activities under the Convention is
achieved through voluntary reporting of
production, import, and export
activities to the Conference of the
Parties. Currently, the Parties to the
Convention are drafting measures for
non-compliance with the Convention.
The key portion of the draft
noncompliance measures includes
suspension from rights of the
Convention for parties found to be
noncompliant. Of particular importance
is suspension from support under
Articles 13 and 14 of the Convention,
which provide for technical and
financial assistance to developing
country Parties and Parties with
economies in transition. Further,
violation of international laws generally
may result in economic sanctions or
could be brought before the
International Court of Justice. Finally,
pursuant to becoming Parties to the
Convention, many countries across the
range of the brown pelican have
adopted national measures to reduce or
eliminate use of various persistent
organic pollutants. These measures are
enforceable through a variety of local
and national laws. Please see the
‘‘Pesticides and Contaminants’’ section
below for additional discussion.
Summary of Factors Affecting the
Species
Section 4 of the Act and its
implementing regulations (50 CFR part
424) set forth the procedures for listing
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species, reclassifying species, or
removing species from listed status. We
may determine a species to be an
endangered or threatened species
because of one or more of the five
factors described in section 4(a)(1) of the
Act, and we must consider these same
five factors in delisting a species. We
may delist a species according to 50
CFR 424.11(d) if the best available
scientific and commercial data indicate
that the species is neither endangered
nor threatened for the following reasons:
(1) The species is extinct; (2) The
species has recovered and is no longer
endangered or threatened (as is the case
with the brown pelican); and/or (3) The
original scientific data used at the time
the species was classified were in error.
A recovered species is one that no
longer meets the Act’s definition of
threatened or endangered. Determining
whether a species is recovered requires
consideration of the same five categories
of threats specified in section 4(a)(1) of
the Act. For species that are already
listed as threatened or endangered, this
analysis of threats is an evaluation of
both the threats currently facing the
species and the threats that are
reasonably likely to affect the species in
the foreseeable future after delisting or
downlisting and the removal or
reduction of the Act’s protections.
A species is ‘‘endangered’’ for
purposes of the Act if it is in danger of
extinction throughout all or a
‘‘significant portion of its range’’ and is
‘‘threatened’’ if it is likely to become
endangered within the foreseeable
future throughout all or a ‘‘significant
portion of its range.’’ The word ‘‘range’’
in the ‘‘significant portion of its range’’
(SPR) phrase refers to the range in
which the species currently exists. The
Act does not define the term
‘‘foreseeable future.’’ However, in a
January 16, 2009, memorandum
addressed to the Acting Director of the
Service, the Office of the Solicitor,
Department of the Interior, concluded,
‘‘* * * as used in the [Act], Congress
intended the term ‘foreseeable future’ to
describe the extent to which the
Secretary can reasonably rely on
predictions about the future in making
determinations about the future
conservation status of the species
(M–37021, January 16, 2009).’’
In considering the foreseeable future
as it relates to the status of the brown
pelican, we considered the factors
acting on the species and looked to see
if reliable predictions about the status of
the species in response to those factors
could be drawn. We considered the
historical data to identify any relevant
existing trends that might allow for
reliable prediction of the future (in the
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form of extrapolating the trends). We
also considered whether we could
reliably predict any future events that
might affect the status of the species,
recognizing that our ability to make
reliable predictions into the future is
limited by the variable quantity and
quality of available data.
For the purposes of this analysis, we
will evaluate whether the currently
listed species, the brown pelican,
should be considered threatened or
endangered. Then we will consider
whether there are any portions of the
brown pelican’s range in danger of
extinction or likely to become
endangered within the foreseeable
future. The following analysis examines
all five factors currently affecting, or
that are likely to affect, the listed brown
pelican populations within the
foreseeable future.
A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Nesting Habitat
Brown pelicans breed annually from
spring to summer above 30 degrees
north latitude, annually from winter to
spring between 20 and 30 degrees north
latitude, and irregularly throughout the
year on 8.5- to 10-month cycles below
20 degrees north latitude (Shields 2002,
p. 12). Brown pelicans usually breed on
small, coastal islands free from
mammalian predators. Brown pelicans
use a wide variety of nesting substrates.
Nests are built on the ground when
vegetation is not available, but when
built in trees, they are about 1.8 meters
(m) to 12.2 m (6 to 40 feet (ft)) above the
water’s surface (McNease et al. 1992, p.
´
252; Jimenez 2004, pp. 12–17).
Along the Pacific Coast of California
south to Baja California and in the Gulf
of California, brown pelicans nest on
dry, rocky substrates, typically on offshore islands (Service 1983, pp. 5–6).
Along the U.S. Gulf Coast, brown
pelicans mainly nest on coastal islands
on the ground or in herbaceous plants
or low shrubs (Shields 2002, p. 13;
Wilkenson et al. 1994, pp. 421–423), but
will use mangrove trees (Avicennia
spp.) if available (Lowery 1974, p. 127;
Blus et al. 1979a, p. 130). In some areas
of the Caribbean, along the Pacific Coast
of Mexico, and the Galapagos Islands,
mangroves (Avicennia spp., Rhizophora
spp., Laguncularia spp.) are the most
common nesting substrate, although
other substrates are used as well
(Collazo 1985, pp. 106–108; Guzman
and Schreiber 1987, p. 276; Service
1983, p. 15; Shields 2002, p. 13).
Various types of tropical forests, such as
tropical thorn and humid forests, also
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provide nesting habitat for brown
pelicans in southern Mexico, South and
Central America, and the West Indies
(Collazo 1985, pp. 106–108; Guzman
and Schreiber 1987, p. 2). Peruvian
brown pelicans (found in Peru and
Chile) nest only on the ground (Shields
2002, p. 13).
Nesting habitat destruction from
coastal development. Within the United
States, the majority of brown pelican
nesting sites are protected through land
ownership by conservation
organizations and local, State, and
Federal agencies. We are not aware of
any losses of brown pelican nesting
habitat to coastal development within
the United States. In countries outside
of the United States, some coastal and
mangrove habitat used by brown
pelicans has been lost to recreational
and other coastal developments (Collazo
et al. 1998, pp. 63). Mainland nesting
colonies in Sinaloa and Nayarit, Mexico,
have been impacted by increasing
mariculture (the cultivation of marine
life) and agriculture through habitat
degradation, disturbance, and some
removal of mangrove habitat (Anderson
et al. 2003, pp. 1097–1099; Anderson
2007), although the extent of impacts is
unknown. Van Halewyn and Norton
(1984, p. 215) cited cutting and loss of
mangrove habitat as a threat for
seabirds, including brown pelicans, in
the Caribbean. Aside from these limited
accounts, we are not aware of any
significant losses of brown pelican
nesting habitat from coastal
development anywhere within its range.
Some destruction of current and
potential brown pelican nesting habitat
is likely to occur in the future. However,
a large number of brown pelican nesting
sites throughout the species’ range are
currently protected (see discussion
below). In some cases, loss of mangrove
habitat has been specifically cited.
However, brown pelicans do not nest
exclusively in mangroves. They utilize a
variety of nesting substrates and readily
colonize new nesting sites in response
to changing habitat conditions. For
example, Collazo et al. (1998, p. 63)
documented the loss of one nesting site
in Puerto Rico, but stated the belief that
the pelicans relocated to a new nesting
colony nearby (see also discussion of
colonization of new sites under ‘‘Storm
effects, weather, and erosion impacts to
habitat’’). Destruction of nesting habitat
is likely to affect brown pelicans on a
local scale only where nesting colonies
overlap with coastal or mariculture
development. In cases where nesting
habitat destruction results in the loss of
a nesting site, it is likely to be limited
to a single season of lost reproduction
because birds will likely disperse to
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other colonies or establish a new colony
in a new location. Because numerous
brown pelican nesting sites are
protected, brown pelicans may relocate
to new nesting sites if any unprotected
sites are destroyed, and any loss of
nesting habitat is likely to result in only
limited loss of reproduction that will
not affect population levels, we do not
believe that nesting habitat destruction
from coastal development currently
threatens brown pelicans, nor do we
believe it will become a threat that
endangers the brown pelican throughout
all of its range in the foreseeable future.
Storm effects, weather, and erosion
impacts to habitat. Many nesting islands
along the U.S. Gulf Coast have been
impacted by wave action, storm surge
erosion, and a lack of sediment
deposition (McNease and Perry 1998, p.
9), resulting in loss or degradation of
nesting habitat. Since 1998, nesting
habitat east of the Mississippi River in
Louisiana has undergone continual
degradation or loss from tropical storms
and hurricanes, resulting in a reduced
number of successfully reared brown
pelican young in this area (Hess and
Linscombe 2006, p. 4). In 2003 and
2004, brown pelican nesting and
reproduction was distributed
approximately equally between areas
east and west of the Mississippi River.
After tropical storms in 2004, nesting
habitat east of the Mississippi River was
reduced, resulting in a shift to 95
percent of nesting and reproduction to
west of the Mississippi River. In 2005,
hurricanes Katrina and Rita resulted in
approximately 349 km2 (217 mi2) of
coastal land loss (Barras 2006, p. 4).
This figure represents total coastal land
loss, including interior marshes.
Although a figure for barrier island loss
would be a more appropriate measure of
impacts to brown pelicans, we are not
aware of any recent, comprehensive
analysis of barrier island loss. Previous
estimates of loss did not include the
benefits of numerous restoration
projects discussed below. While
Louisiana’s brown pelican nesting
islands east of the Mississippi River
were reduced by over 70 percent and
what remains is vulnerable to overwash
from future storm tides, at the time,
these islands supported only about 5
percent of the total Louisiana
population of brown pelicans (Hess and
Linscombe 2006, pp. 3, 6; Harris 2006).
Louisiana brown pelican nesting islands
west of the Mississippi River, which
accounted for 95 percent of the 2005
brown pelican breeding population,
were degraded, but still supported the
four main nesting colonies (Hess and
Linscombe 2006, p. 5) (see discussion of
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nesting in Louisiana under
‘‘Distribution and Population
Estimate’’).
In some instances, brown pelicans
have responded to losses of breeding
sites by dispersing and using other areas
(Hess and Durham 2002, p. 7). Hess and
Linscombe (2001, p. 5) believe that a
shift in nesting from the Baptiste
Collette area to Breton Island in
Louisiana was the result of high
Mississippi River levels and associated
muddy water, which limited sight
feeding. Additionally, two new brown
pelican nesting colonies were
established between 2000 and 2005 on
Baptiste Collette and Shallow Bayou
(Hess and Linscombe 2006, p. 5).
Wilkinson et al. (1994, p. 425) reported
the loss of large brown pelican nesting
colonies on Deveaux Bank in South
Carolina following a hurricane and
subsequent movement and use of new
nesting locations on that island and on
Bird Key Stono. Hess and Linscombe
(2001, p. 4) believe that tropical storm
and hurricane-induced habitat damage
to the Chandeleur Islands contributed to
the initial dispersal of pelicans to
southwest Louisiana and the formation
of a nesting colony on newly created
habitat at the Baptiste Collette bar
channel.
While pelicans generally exhibit nest
site fidelity, they can also demonstrate
flexibility and adaptability. In Texas
and Louisiana they have established
breeding colonies on islands artificially
created or enhanced by material
dredged by the U.S. Army Corps of
Engineers (Corps) from nearby ship
channels (Hess and Linscombe 2001,
pp. 5–6; Hess and Linscombe 2006, p.
5). For example, Little Pelican Island
and Alligator Point in Texas are
maintained by the disposal of dredged
material (Yeargan 2007). The Corps in
Louisiana beneficially uses
approximately 8.5 million m3 (11.1
million yds3) of dredged material each
year in the surrounding environment
(Corps 2004, p. xi). For example,
dredged material was used to retard
erosion and secure Queen Bess Island as
brown pelican nesting habitat (McNease
et al. 1994, p. 8). It was also used to
restore and enhance brown pelican
habitat on Raccoon Island in 1987 and
Last Island in 1992 following Hurricane
Andrew (McNease and Perry 1998, p.
10; Hess and Linscombe 2001, p. 5). Use
of these islands by pelicans
demonstrates both the utility of these
artificially generated habitats and the
pelican’s ability to find and establish
nesting colonies on them.
While storms in Louisiana and the
U.S. Gulf Coast are expected to continue
in perpetuity, there are numerous
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projects that are intended to protect the
coast from this land loss. Coastal habitat
protection and restoration have been
and will continue to be priorities for
Louisiana, since coastal land loss has
much broader negative implications to
the State economy, oil and gas
production, navigation security,
fisheries and flyways, and strategic
petroleum reserves. The Coastal
Wetlands Planning, Protection, and
Restoration Act of 1990 (CWPPRA),
which provides Federal grants to
acquire, restore, and enhance wetlands
of coastal States, is one of the first
programs with Federal funds dedicated
exclusively to the long-term restoration
of coastal habitat (104 Stat. 4779). As of
April 2006, 10 CWPPRA barrier island
restoration projects in Louisiana have
been implemented (costing over 75.8
million dollars), with another 9
currently under construction or
awaiting construction. Several of these
directly enhance or protect current
brown pelican nesting habitat (for
example, Raccoon Island), while the rest
occur on islands that were historically
used or could be used for nesting in the
future (Louisiana Coastal Wetlands
Conservation and Restoration Task
Force 2006, p. 13).
Two other restoration plans being
implemented in coastal Louisiana are
the Louisiana Coastal Area Ecosystem
Restoration Plan (LCA) and Louisiana’s
Comprehensive Master Plan for a
Sustainable Coast (State Master Plan).
The LCA, administered by the Corps of
Engineers with State cost-share
assistance, focuses on the protection of
coastal wetlands, including barrier
island restoration. The State Master Plan
includes barrier island protection and
restoration as a key component. In
addition, Louisiana’s Coastal Impact
Assistance Program (CIAP) also
provides funding for barrier island
restoration. The State Master Plan serves
as Louisiana’s overarching document to
guide hurricane protection and coastal
restoration efforts in the State. While
none of these plans are considered
existing regulatory mechanisms for the
purposes of this delisting rule and they
are not designed specifically to benefit
brown pelicans, they may provide
opportunities for us to monitor and to
minimize the threats to brown pelicans
from habitat loss and degradation
caused by storms in the Louisiana Gulf
Coast region after the species is delisted.
They also demonstrate the level of
importance State and Federal agencies
place on maintaining and protecting
those areas.
In other portions of the species’ range,
storms and weather conditions may also
remove or degrade vegetation used for
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nesting by brown pelicans. Hurricanes
(category 3 or higher) such as Hugo and
Georges have severely affected red
(Rhizophora mangle) and black
(Avicennia germinans) mangrove habitat
in Puerto Rico. Other coastal trees such
as Bursera simaruba and Pisonia
subcordata, which are prime nesting
trees for pelicans in the U.S. Virgin
Islands, have also been completely
defoliated or torn down by hurricanes
(Saliva 1989). Mangroves and other
coastal trees may either be uprooted,
completely defoliated, or killed (through
dislodging of submerged roots by strong
wave action), and several breeding
seasons may pass before those areas
recover. Similar effects of hurricanes
and storms on nesting vegetation would
be expected in other areas where brown
pelicans nest in trees (some areas in the
Caribbean, portions of the Pacific coast
of Mexico, and parts of Central and
South America). Along the U.S. Gulf
Coast, mangroves can be killed off by
extreme cold weather (Blus et al. 1979a,
p. 130; McNease et al. 1992, p. 225;
McNease et al. 1994, p. 6). Coastal black
mangroves, decimated by freezes since
the 1980s, were historically the nesting
shrub of choice for brown pelicans in
Louisiana, but now clumps of
vegetation, like dense stands of
nonwoody plants or low woody shrubs,
are used (McNease et al. 1992, p. 225;
Shields et al. 2002, p. 23).
While localized losses and
degradation of nesting habitat from
hurricanes, storms, and erosion have
been documented (Wilkinson et al.
1994, p. 425; Hess and Linscombe 2006,
p. 4), brown pelicans have demonstrated
that they are capable of recovering from
such losses. For example, brown pelican
nests producing young in Louisiana
have generally increased from a low in
1993 of 5,186 to a high of 16,501 in 2004
(Hess and Linscombe 2006, pp. 5, 13).
During this timeframe, numerous
tropical storms and hurricanes have
made landfall on the Louisiana coast
(Hess and Linscombe 2006, pp. 9–11).
As of May 2006, less than a year after
Hurricanes Katrina and Rita, Hess and
Linscombe (2007, p. 4) noted a total of
8,036 nests in 15 colonies. Additionally,
brown pelicans have shown they are
capable of dispersing from nesting sites.
Examples of this dispersal are the
natural expansion and population
growth observed following the
reintroduction program in Louisiana
(McNease and Perry 1998, p. 1) and
more recently with the establishment of
a new nesting colony at Rabbit Island
(Hess and Linscombe 2003, p. 5). It is
reasonable to expect island erosion will
continue; however, it is also reasonable
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to expect State and Federal agencies to
continue active maintenance and
restoration of barrier islands through
programs such as the CWPPRA and the
State Master Plan.
We lack data on the effects of storms
and erosion elsewhere in the range of
the brown pelican. However, outside of
the Gulf of Mexico and Caribbean,
storms generally are less frequent and
less severe. It is evident from the
information on pelican responses to
storms in the Gulf of Mexico that they
are capable of successfully adapting to
the changes that storms bring. In
addition, brown pelicans are broadly
distributed along the Gulf of Mexico,
nesting at 15 sites in Louisiana in 2006
(LDWF 2007, pp. 1, 3) and 12 sites in
Texas in 2006 (Service 2006, p. 2). The
species’ broad distribution and multiple
nesting colonies reduce the risk that any
single storm would affect the entire Gulf
coast population of brown pelicans.
Therefore, we believe that habitat
modification or destruction of brown
pelican nesting habitat by storms or
coastal erosion will not endanger the
brown pelican throughout all of its
range in the foreseeable future.
Nesting Habitat Protection
A number of factors may affect the
quantity and quality of brown pelican
nesting habitat from year to year.
However, almost all the U.S. nesting
sites are protected from manmade
habitat destruction and human
disturbance, and a significant number of
nesting sites outside the United States
are also protected. Protections include
designations as wildlife refuges,
biosphere reserves, and national parks,
as well as land ownership and
protection by conservation
organizations and local, State, and
Federal governments. Because these
protections are designed not only to
protect brown pelicans, but other
resources as well, such as other species
of colonial waterbirds, and wetland,
coastal, and marine habitats, we do not
expect these protections to change when
the brown pelican is delisted.
Gulf of Mexico Coast. Many of the
Texas islands used by brown pelicans
are leased, managed, and monitored by
local chapters of the National Audubon
Society (Audubon) (Audubon 2007a, p.
1). In Texas, Audubon staff assess the
conditions of brown pelican islands
throughout the year (Yeargan 2007) and
implement management actions to
address issues such as erosion and fire
ant control. Additionally, there are local
‘‘Bird Wardens’’ that patrol the islands
regularly (Audubon 2007b, p. 1). The
two largest brown pelican nesting
colonies in Texas, both in Corpus
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Christi Bay, Texas (Sundown Island,
owned by the Port of Corpus Christi,
and Pelican Island, owned by the Texas
General Land Office), are part of the
Texas Audubon Society’s Coastal
Sanctuaries program (Yeargan 2007;
Audubon 2007b, p. 1; Service 2007b,
p. 2). Audubon also owns North Deer
Island, which houses the most
productive waterbird colony in
Galveston Bay and is the largest natural
island remaining in the bay (Audubon
2007c, p. 1). A third major nesting site,
Little Pelican Island, Galveston Bay, is
owned by the U.S. Army Corps of
Engineers (Corps) (Yeargan 2007).
Audubon, in cooperation with the
Corps, Texas Parks and Wildlife
Department, and the Service, has placed
signs around Little Pelican Island
advising the public to avoid landing on
the island during the nesting season
(Service 2007b, p. 3).
Also in Galveston Bay, Evia and
Midbay islands, owned by the Port of
Houston, are important brown pelican
nesting islands, and Alligator Point in
Chocolate Bayou, owned by the Texas
General Land Office, also supports
breeding brown pelicans (Yeargan
2007). Brown pelicans are counted
annually as part of the Texas Colonial
Waterbird Survey (Service 2006, p. 1;
Erfling 2007). Signs advising the public
to avoid landing were posted at each
island listed above and later lost during
Hurricane Ike in 2008; however, the
signs are to be replaced after the
hurricane debris is removed (Erfling
2009).
Louisiana’s North Island and Breton
Island, two pelican nesting islands
within the Chandeleur Islands chain,
are part of the Service’s Breton National
Wildlife Refuge system (GulfBase 2007,
p. 1). Signs are posted at the edge of the
water indicating that the site is closed
to human intrusion during the nesting
season. In addition, during the nesting
season, law enforcement personnel
patrol the islands during periods of high
human presence, such as on weekends
and holidays (Fuller 2007c). One of
Louisiana’s largest pelican nesting
colonies, Raccoon Island, in addition to
Wine Island, East Island, Trinity Island,
and Whiskey Island, are part of the Isles
Dernieres Barrier Islands Refuge owned
and managed by the LDWF, which
restricts public access (Fuller 2007d).
Additionally, there are several other
small, intermittently used nesting
colony sites, such as Martin and Brush
islands, that are privately owned.
However, these sites are remote and are
likely only subject to occasional
offshore recreational and commercial
fishing activity.
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West Indies. The two nesting sites
documented by Collier et al. (2003, p.
113) on St. Maarten are protected: Fort
Amsterdam as a registered and
protected historic site, and Pelikan Key
as part of a marine park. In addition,
both sites have been proposed as
Important Bird Areas (Society for the
Conservation and Study of Caribbean
Birds 2006, pp. 11–12).
In Puerto Rico and the U.S. Virgin
Islands, most breeding colonies of
brown pelicans are located within
Commonwealth or Federal protected
areas. Cayo Conejo, on the south coast
of Vieques Island, Puerto Rico, is one of
the two most active and largest brown
pelican nesting colonies in Puerto Rico
(Saliva 2003). The U.S. Navy began
using the eastern portion of Vieques
Island for training exercises in the early
years of World War II, and acquired the
eastern and western portions of the
island between 1941 and 1943
(Schreiber 1999, pp. 8, 13, 18–21). Since
that time, it has been used in varying
intensities for activities including
amphibious landings, naval gunfire
support, and air-to-ground training
(Service 2001, p. 4). In May 2003, the
Navy ceased operations on Vieques
Island via the Floyd D. Spense Defense
Authorization Act of 2001 and
transferred these lands to the Service,
which subsequently designated it as the
Vieques Island National Wildlife
Refuge.
In the U.S. Virgin Islands, brown
pelican colonies are fairly inaccessible
on high cliffs or steep cays (Collazo
1985, pp. 106–108; Saliva 1996b);
therefore, it is unlikely that human
intrusion would be a major factor
affecting pelican reproduction in those
colonies.
The six nesting sites in Cuba
identified by Acosta-Cruz and Mugica´
Valdes (2006, pp. 32–33) are within
areas identified as wetlands of
international importance under the
Convention on Wetlands of
International Importance especially as
Waterfowl Habitat. The convention
itself does not provide specific
protections of identified wetlands, but
does commit the parties to the
convention to formulate and implement
planning for the conservation and
management of wetlands within their
countries. One of the brown pelican
´
sites in Cuba, Refugio de Fauna Rıo
´
Maximo, is additionally protected as a
wildlife refuge (Acosta-Cruz and
´
Mugica-Valdes 2006, pp. 32–33).
California and Pacific Coast of
Mexico. Pelican nesting colonies in
California occur within Channel Islands
National Park and are protected from
human disturbance and coastal
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development. West Anacapa Island,
where approximately 75 percent of the
SCB population nests (Gress et al. 2003,
p. 15), is designated as a research
natural area by Channel Islands
National Park and closed to the public
(NPS 2004, p. 4). To protect pelican
nesting areas, Santa Barbara Island trails
are seasonally closed (NPS 2006, p. 1),
and Scorpion Rock off Santa Cruz Island
is permanently closed to the public
(NPS 2004, p. 2). In 1980, the waters
adjacent to the Channel Islands were
designated as a National Marine
Sanctuary (15 CFR 922). This
designation implements restrictions
which include, but are not limited to,
(1) no tankers and other bulk carriers
and barges, or any vessel engaged in the
servicing of offshore installations within
1.8 kilometers (km) (1.15 miles (mi)); (2)
no motorized aircraft at altitudes less
than 305 m (1,000 ft) over the waters
within 1.8 km (1.15 mi); and (3) no
exploring for, developing, or producing
oil and gas unless authorized prior to
1981 (NOAA 2006, Appendix C).
Additionally, in 2003, the California
Department of Fish and Game (CDFG)
designated the waters adjacent to
nesting brown pelican habitat on West
Anacapa island as a Marine Reserve,
increasing protections for that colony by
prohibiting fishing and other boating
activities at depths of less than 37 m
(120 ft) from January 1 to October 31 of
each year (California Code of
Regulations, Title 14, Sections 27.82,
630, and 6321). In 1999, commercial
squid fishing boats operating offshore of
West Anacapa and Santa Barbara
islands during the pelican breeding
season, presumably because the
(nonlocal) fishermen were not aware of
the closure during the breeding season,
used bright lights at night to attract
squid to the surface (Gress 1999, p. 1).
Use of lights at night was associated
with brown pelican nest abandonment,
chick mortality, and very low
productivity (Gress 1999, pp. 1–2).
Squid fishing has been observed around
the Channel Islands in recent years,
although it has not occurred near the
colonies at a noticeable level since 1999
(Whitworth et al. 2005, p. 19). In 2004,
the California Fish and Game
Commission adopted the requirement of
light shields and a limit of 30,000 watts
per boat operating around the Channel
Islands (CDFG Regulations, Section 149,
Title 14, CCR). Although occasional
disturbances may occur during the
breeding season, such as illegal boating
within the Marine Sanctuary, we believe
the protections and active enforcement
by the National Park Service (NPS) and
CDFG have ensured that all nesting
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colonies in California remain relatively
disturbance free.
As noted above, Mexico’s nesting
brown pelicans are monitored annually
as an indicator species in the Gulf of
California (Godinez et al. 2004, p. 48).
All of the island nesting colonies and
many of the mainland Mexico nesting
colonies are protected from habitat
destruction or modification by Mexican
law because the sites are federally
protected and designated as either
Biosphere Reserve Areas for Protection
of Flora and Fauna or National Parks
(Anderson and Palacios 2005, p. 16;
Carabias-Lilio et al. 2000, p. 3).
Central America, South America, and
Caribbean Coast of Mexico. Isla Contoy
Reserva Especial de la Biosfera off the
coast of Cancun, Quintana Roo, Mexico,
is Mexico’s largest brown pelican
nesting colony on the Caribbean coast.
It is currently protected as a National
Park within a Biosphere Reserve.
Visitation is limited and strictly
controlled to minimize impacts to the
seabirds that nest and roost there.
Guatemala—Eisermann (2006, p. 63)
identified 12 sites where brown pelicans
are present within Guatemala, but did
not indicate whether any of these are
nesting sites. Of these 12 sites, 10 have
some level of conservation as either
Wildlife Refuges, National Parks, Areas
of Multiple Use, or private protected
areas (Eisermann 2006, p. 13).
Honduras—In Honduras, two of the
four identified nesting sites for brown
pelicans are currently protected:
Monumento Natural Marino del
´
Archipielago de Cayos Cochinos and
Laguna de Los Micos within Parque
Nacional Blanca Jeannette Kawas
(Thorn et al. 2006, pp. 8, 11, 29). A third
nesting area, the cays of Isla Utila, has
been proposed for protection as Refugio
de Vida Silvestre Cayos de Utila and
Reserva Marina Utila (Thorn et al. 2006,
p. 9).
Nicaragua—Although Zolotoff-Pallais
and Lezama (2006, p. 79) do not
indicate any nesting sites for brown
pelicans, they indicate that brown
pelicans occur at four sites designated
as wetlands of international importance
under the Convention on Wetlands of
International Importance especially as
Waterfowl Habitat.
Costa Rica—In Costa Rica, the three
major brown pelican nesting sites
reported by Quesada (2006, p. 34), Isla
Guayabo, Isla Negrita, and Isla Pararos,
are protected as Biological Reserves. A
fourth site, Isla Verde, identified as a
roosting location for brown pelicans, is
protected as a National Park (Quesada
2006, p. 34).
Panama—Angehr (2005, pp. 23, 26,
30, 34) identifies four nesting sites used
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by brown pelicans in Panama that are
on lands with some official protective
status: (1) Isla Barca Quebrada, within
Coiba National Park; (2) Iguana Island,
within Isla Iguana Wildlife Refuge; (3) a
group of small islands mostly within the
Taboga Wildlife Refuge; and (4) Pearl
Islands, owned by the Panamanian
environmental organization ANCON
(National Association for the
Conservation of Nature). There are many
more nesting areas in Panama, but they
lack protective status.
Colombia—In Colombia, the seven
sites where brown pelican were
documented to occur by Moreno and
Buelvas (2005, pp. 11, 57) are included
in a system of protected areas or as part
of sanctuaries for wildlife and plants.
Venezuela—In Venezuela, Rodner
(2006, p. 28) indicates that at least 9 of
the 25 nesting colonies for brown
pelicans are protected as either Parques
Nacional, Monumentals Natural, or
Refugios de Silvestre.
Ecuador—About 87 percent of the
Galapagos Islands are a National Park
(Exploring Ecuador 2006, p. 1), and
commercial and tourist access to the
Park is regulated by the government of
Ecuador to protect natural resources
(Service 2007a, p. 23). The resident
human population on the Galapagos
Islands has expanded in recent years, as
has the number of tourists (Charles
Darwin Foundation 2006, p. 13). The
Charles Darwin Foundation, which
works in the islands under an agreement
with the government of Ecuador, has
developed a strategic plan to address the
management of increasing human
presence in the islands (Charles Darwin
Foundation 2006, p. 7). The plan’s
general objective is to ‘‘forge a
sustainable Galapagos society in which
the people who inhabit the islands will
act as agents of conservation.’’
Peru—Proabonos, an agency in Peru’s
Ministry of Agriculture, protects and
manages brown pelican nesting islands
(Zavalaga et al. 2002, p. 9; Proabonos
2006). Additionally, Franke (2006, p. 8)
indicates brown pelicans occur at four
protected sites, although it is not clear
whether these are nesting sites as well:
Santuario Nacional Los Manglares de
Tumbes, Zona Reservada Los Pantanos
de Villa, National Reserve Paracas, and
´
Santuario Nacional Lagunas de Mejıa.
Estimated increases in the brown
pelican population along coastal Peru
have been attributed to protective
measures by the Government of Peru.
The Ministry of Agriculture’s Forest and
Wild Fauna Management Authority
(IRENA) lists the brown pelican as
endangered, and provides prohibitions
against take of the species without a
permit (Taura 2006).
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Chile—Simeone and Bernal (2000, p.
´
˜
450) reported that Isla Pajaro Nino in
Chile has been designated a Nature
Reserve by the Chilean government for
the protection of Humboldt penguins,
brown pelicans, and other seabirds. The
breakwater connecting the island to the
mainland has controlled access, which
has reduced human disturbance
(Simeone and Bernal 2000, p. 455).
In summary, efforts to conserve
nesting habitat are positively affecting
nesting brown pelicans, resulting in an
overall rangewide recovery. Although
loss of nesting habitat has occurred on
a local scale, for instance, in Puerto Rico
(Collazo et al. 1998, p. 63) and Mexico
(Anderson et al. 2003, p. 1099), we have
no evidence that nesting habitat is
limiting pelican populations on a
regional or global scale. Threats from
human disturbance of nesting colonies
throughout most of the species’ range
have been abated through protection
efforts, including federal and state
ownership and management,
designation of National Parks and
Biosphere Reserves, signage to deter
people from entering colonies, and
restricted access. While nesting habitat
at a local scale is lost to storms and
erosion, particularly in the Gulf of
Mexico (McNease and Perry 1998, p. 9),
birds have been found to disperse to and
colonize other natural areas (Hess and
Durham 2002, p. 7) and manmade
islands (Hess and Linscombe 2006, pp.
3, 6; Harris 2006).
Roosting Habitat
Disturbance-free roosting habitat is
essential for brown pelicans throughout
the year, for drying and maintaining
plumage, resting, sleeping, and
conserving energy (Jaques and Anderson
1987, pp. 4–5). Roosts also act as
information centers for social
facilitation. Essential characteristics of
roost sites include: Proximity to food
resources; physical barriers to minimize
predation and disturbance; sufficient
size for individuals to interact normally;
and protection from adverse
environmental conditions, such as wind
and surf (Jaques and Anderson 1987, p.
5). Communal roosts occur on offshore
rocks and islands; on beaches at mouths
of estuaries; and on breakwaters,
pilings, jetties, sandbars, and mangrove
islets (Jaques and Anderson 1987, pp.
14, 19; Shields 2002, p. 7). Brown
pelicans have two types of roosts, day
and night roosts. Night roosts need to be
larger and less accessible to predators
and human disturbance than day roosts
(Jaques and Anderson 1987, p. 27;
Jaques and Strong 2003, p. 1). Along the
Pacific Coast, brown pelicans use roost
sites that are different from nest sites
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(Jaques and Anderson 1987, pp. 14, 19;
Briggs et al. 1981, pp. 7–8). In other
areas, brown pelicans generally use
their nesting grounds as roosting
grounds year round (Saliva 2003; Hess
and Durham 2002, p. 1; Hess and
Linscombe 2001, p. 1; King et al. 1985,
p. 204). Because brown pelicans also
use nesting sites as roosting sites and
most of these nesting areas are already
protected, as described above, we
believe roosting habitat is also generally
adequately protected. However, we have
identified southern California as one
area where roosting habitat may be
limited. We discuss the adequacy of
protections of southern California
roosting habitat and its effects on the
species below.
While not known to be a concern in
other portions of the brown pelican’s
range, natural roost habitat is limited
along the southern California coast due
to a lack of rocky substrate, as well as
coastal development and wetland filling
(Jaques and Strong 2003, p. 1). Most
roosts in southern California occur on
jetties and breakwaters under
jurisdiction of the Corps, although
private structures such as barges and oil
platforms also provide significant roost
habitat (Strong and Jaques 2003, p. 20).
Night roost habitat is further limited to
large areas where disturbance is
minimal, which may be causing
pelicans to expend unnecessary energy
to fly between daytime roosting/foraging
areas along the mainland and distant
night roosts in the Channel Islands
(Jaques et al. 1996, p. 46; Jaques and
Strong 2003, p. 12).
In California, all rocks, islands,
pinnacles, and exposed reefs above
mean high tide within 22.2 km (13.8 mi)
of shore are included within the
California Coastal National Monument,
managed by the U.S. Bureau of Land
Management (U.S. Bureau of Land
Management 2005, pp. 1–3).
Management includes monitoring and
protecting geologic formations and the
habitat they provide for seabirds and
other wildlife (U.S. Bureau of Land
Management 2005, pp. 1–3). Many
pelican roost sites are on protected
rocks and islands within the California
Coastal National Monument.
The central California coast supports
an important temporal component of
pelican roosting habitat, supporting 69
to 75 percent of pelicans in California in
the fall (Strong and Jaques 2003, p. 28).
The Farallon Islands National Wildlife
Refuge and Monterey Bay National
Marine Sanctuary in central California
protect and support roosting habitat (15
CFR 922; Thayer and Sydeman 2004, p.
2; Service 2007c, p. 1). CDFG designated
the waters around the Farallon Islands
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as a State Marine Conservation Area,
and the islands are part of the Gulf of
the Farallons National Marine Sanctuary
(CDFG 2007, p. 7; 15 CFR 922). The
Marine Sanctuaries prohibit aircraft
from flying below 305 m (1,000 ft)
within their boundaries, and limit
allowable uses to research, educational,
and recreational activities. In general,
commercial and recreational uses of
marine resources are prohibited, but
certain commercial and recreational
harvests of marine resources may be
permitted (CDFG 2007, pp. 4–5; 15 CFR
922).
Vandenberg Air Force Base (AFB), in
southern California, consulted under
section 7 of the Act with the Service
regarding the effects of low-flying test
flights, and agreed to avoid flying
directly over roosting pelicans occurring
on their mainland base (Service 2003a,
p. 1). We have consulted with
Vandenberg AFB multiple times
regarding the impacts of missile
launches on roosting pelicans and have
determined that impacts are limited to
a short-term startle effect (Service 1998,
1999, 2003a). A maximum of 30 missile
launches per year at Vandenberg AFB
are estimated (Vanderberg AFB 2008, p.
14). Therefore, potential impacts from
missile launches are minimal because
they are temporary in nature and will
likely only occur a few times per month.
The Sonny Bono Salton Sea National
Wildlife Refuge, inland from San Diego,
is also used for roosting during the postbreeding season, and supports and
protects up to 5,000 pelicans in the
summer within its boundaries (Service
2007d, pp. 1–2). However, roosting
habitat is expected to decrease after the
year 2018 as a result of reductions of
Colorado River water reaching the
Salton Sea (Service 2002, p. 52), which
could decrease the availability of forage
fishes to pelicans and reduce the
suitability of roosting habitat in this area
(Service 2002, pp. 18, 51). The Bureau
of Reclamation will compensate for this
loss by creating new roosting habitat
along the southern California coast
(Service 2002, p. 52).
An atlas of pelican roost sites along
portions of the central and northern
California coasts was completed that
will allow management agencies to
evaluate the overall status of roosting
habitat and help prioritize roost sites for
protection. A similar atlas for the
southern California coast was completed
in January of 2009 (Service 2009a). In
addition, the following restoration plans
include projects that will benefit brown
pelicans, regardless of the brown
pelican listing status: American Trader
Restoration Plan, Command Oil Spill
Restoration Plan, Torch/Platform Irene
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Restoration Plan, Kure/Humboldt Bay
Oil Spill Restoration Plan (KRP),
Stuyvesant/Humboldt Coast Oil Spill
Restoration Plan (SRP), and Montrose
Settlement Restoration Plan (MSRP).
The purpose of these plans is to restore
natural resources, including seabirds,
that were injured as a result of oil spills
and hazardous substance releases along
the California coast. One component of
all these plans is to reduce human
disturbance at roost sites in northern,
central, and southern California through
education, monitoring, and enforcement
(American Trader Trustee Council 2001,
p. 16; Command Oil Spill Trustee
Council 2004, p. 60; Torch/Platform
Irene Trustee Council 2006, p. 33; CDFG
and Service 2008, p. 40; CDFG and
Service 2007, p. 26; MSRP 2005, p. D6–
1). The American Trader Trustee
Council also funded a pilot program in
2004 to create new night roosting
habitat in the form of a floating platform
in the San Diego Bay National Wildlife
Refuge salt ponds. While pelican use
has been limited, the American Trader
Trustee Council is exploring ways to
enhance and improve the platform. The
MSRP also includes roost site creation
and/or enhancement as suitable
restoration projects for the brown
pelican (MSRP 2005, p. D6–1).
While some roosting habitat in the
United States may still be susceptible to
human disturbance, much of the brown
pelican roosting habitat occurs within
protected areas. There are ongoing
efforts to identify and prioritize
important roost sites, reduce
disturbances at these sites, enhance
existing roosts, and create new roost
habitat. Southern California is the only
area we are aware of with potentially
limited roost sites. We have no
information to indicate that roosting
habitat may be limiting elsewhere in the
species’ range. Nevertheless, the limited
number of existing roost sites has had
no known impacts to the species and
the population appears to be stable or
increasing. Therefore, we do not believe
that roost site disturbance will adversely
affect the brown pelican throughout all
of its range in the foreseeable future.
Prey Abundance
Brown pelicans feed on surfaceschooling fish such as menhaden
(Brevoortia spp.), mullet (Mugil spp.),
sardines (Sardinops sagax), and
anchovies (Engraulis spp.), which they
catch by plunge-diving in coastal waters
(Palmer 1962, p. 279; Blus et al. 1979b,
p. 175; Gress et al. 1990, p. 2; Schreiber
et al. 1975, p. 649; Schreiber 1980, p.
744; Kushlan and Frohring 1985, p. 92).
The availability of high quality forage in
the offshore area within 30 to 50 km (18
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to 30 mi) of a colony during the
breeding season is critical to pelicans
for feeding young (Anderson et al. 1982,
p. 28). Additionally, reproductive
success is dependent on abundance and
availability of prey within foraging
distance of the colony (Anderson et al.
1982, pp. 23, 30; Everett and Anderson
1991, p. 133). Therefore, commercial
harvests of pelican prey species have
the potential to affect brown pelican
population dynamics.
Commercial fishing. The MagnusonStevens Fishery Conservation and
Management Act of 1976 (16 U.S.C.
1801 et seq.) requires management plans
for commercial fish species to ensure
optimum yield with guaranteed
perpetuation of that resource and
minimal impact to the ecosystem of
which it is a part. Each coastal region of
the United States is a member of one of
eight Fishery Management Councils,
each of which implements the local
fishery management plan (16 U.S.C.
1801 et seq.).
The Pacific Fishery Management
Council prepared the Anchovy Fishery
Management Plan. Amendment 8 to the
Anchovy Fishery Management Plan,
adopted December 15, 1999 (64 FR
69888), changed the name of the
Anchovy Fishery Management Plan to
the Coastal Pelagic Species Fishery
Management Plan (CPSFMP) and added
Pacific sardine (Sardinops sagax),
Pacific mackerel (Scomber japonicus),
jack mackerel (Trachurus symmetricus),
and market squid (Loligo opalescens) to
the fishery management unit (CPSFMP
1998, p. 1–1). Amendment 8 divided
these species into the categories of
actively managed and monitored.
Harvest guidelines for actively managed
species, Pacific sardine and Pacific
mackerel, are based on formulas applied
to current biomass estimates and
designed to ensure that adequate forage
is available for seabirds, marine
mammals, and other fish. There are no
harvest guidelines for the monitored
species (northern anchovy, jack
mackerel, and market squid) because
they are not currently intensively
fished, although harvest and abundance
data will be monitored (CPSFMP 1998,
pp. 4–5). The northern anchovy fishery
essentially ceased in 1983 due to a
depressed market. The depressed
market for northern anchovy is thought
to be a long-term or possibly permanent
condition, although this fishery
continues today at a minimal level
(CDFG 2001, pp. 303–305). A
comprehensive assessment of the
northern anchovy fishery will be
conducted if the annual harvest
approaches 25,000 metric tons (mt)
(25,097 tons); however, the annual
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harvest as of 1999 was estimated to be
only about 7,000 mt (6,889 tons) of an
estimated biomass of 388,000 mt
(381,872 tons) (Service 1999, pp. 1–2).
On June 10, 1999, the Service
determined that Amendment 8 to the
Anchovy Fishery Management Plan will
not adversely affect brown pelicans in
California because it would not decrease
the availability of fish to pelicans
(Service 1999, p. 1). The CPSFMP (1998,
pp. 2–5) will continue to ensure that
adequate forage is available to pelicans
if economic conditions change and
northern anchovies become more
intensively fished. The CPSFMP will
also ensure that other forage fishes used
by pelicans, such as Pacific sardines and
Pacific mackerel, are also managed to
preserve adequate forage reserves
(CPSFMP 1998, pp. 2–5).
Implementation of the CPSFMP is not
dependent on the brown pelican’s status
as an endangered species, and should
not be affected by this delisting rule.
The central subpopulation of the
northern anchovy extends south of the
U.S. border along the west coast of Baja
California, Mexico. However, there is no
bilateral agreement between the United
States and Mexico regarding the
management of this subpopulation, and
the Mexican fishery is managed
independently and not restricted by a
quota (CDFG 2001, p. 304). The
Coronados Islands pelican population
may have suffered reduced breeding
success during the late 1970s as a result
of intensive commercial anchovy
harvests in Mexico (Anderson and Gress
1982, p. 130). Declines in the anchovy
population in the early 1980s may have
been caused by intensive harvesting in
Mexico that far exceeded the California
fishery (Service 1983, p. 57). Similar to
the U.S. fishery, anchovy harvests in
Mexico have decreased sharply over
time, from an average 86,363 mt (85,000
tons) per year from 1962 to 1989, to an
average of 3.65 mt (3.6 tons) from 1990
to 1999 (CDFG 2001, p. 303). However,
if economic conditions change and
anchovies become more intensively
harvested in Mexico, availability of
anchovies for pelicans could be
reduced.
While no brown pelican prey species
appear to be currently regulated by the
Gulf of Mexico Fishery Management
Council or the Caribbean Fishery
Management Council (Web sites
accessed: https://www.gulfcouncil.org/,
and https://www.caribbeanfmc.com/) in
the United States, regulations under
authority of the Magnuson-Stevens
Fishery Conservation and Management
Act are sufficient to protect prey
abundance for brown pelicans,
including brown pelican food species
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currently being commercially fished and
any that may be in the future. Therefore,
we do not believe that commercial
fishing will endanger the brown pelican
or its prey throughout the United States,
Mexico, and Caribbean portion of its
range in the foreseeable future.
We do not have information from
other countries on commercial fishery
impacts to brown pelican prey
abundance. However, we have no
evidence to suggest that commercial
fishing is limiting brown pelican
populations. Populations of brown
pelicans in Central and South America
are generally large with stable or
increasing trends, indicating that food
resources are not limiting.
˜
El Nino and Freeze Events. A mixture
of subarctic and tropical waters,
upwelling events, and varying depths of
the Pacific Ocean result in seasonal,
inter-annual (between year), and longterm variability in fish availability for
brown pelicans (Dailey et al. 1993, pp.
˜
11–13). El Nino events that occur
periodically in the Pacific Ocean are
characterized by warm, nutrient-poor
water and reduced productivity (Dailey
et al. 1993, p. 11; Leck 1973, p. 357;
Duffy 1983b, p. 687), thus reducing
brown pelican reproductive success and
causing mortality in pelican chicks
(Hayward 2000, p. 111). Pelicans have
the flexibility to respond to changes in
food supplies through variable
reproductive rates, although a long-term
decline in food abundance could have
serious impacts on the pelican
population (Anderson et al. 1982, p. 30).
˜
An incidental effect of El Nino is
movement of brown pelicans into
developed areas, presumably in search
of food, exposing them to collision
hazards with structures and vehicles
(Leck 1973, p. 357). During the 1997 El
˜
Nino event, an increase was reported in
the local pelican population from 200 to
4,000 birds within a few weeks within
the city of Arica, Chile (CNN 1997, p.
˜
1). El Nino events are generally limited
to a single breeding season, and are not
likely to result in long-term population
declines (Dailey et al. 1993, p. 11).
McNease et al. (1994, p. 10) found
that severe freezes limited feeding due
to surface ice formation. Fish mortality
related to freezes also negatively
impacts the pelican’s food supply on a
short-term basis (McNease et al. 1994, p.
10). However, these events are typically
localized and restricted to a single
season in duration.
˜
El Ninos and severe freezes may
impact brown pelicans on a short-term,
localized basis, but they do not pose a
rangewide threat to the continued
existence of the species. The pelican is
a long-lived species that has evolved
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with natural phenomena such as
variation in food resources, winter
storms, and hurricanes, such that
sporadic breeding failures have little
effect on long-term population stability
(Shields 2002, p. 23). These factors are
only significant when population sizes
are small and reproduction is limited (as
was the case in the late 1960s due to
impaired breeding success caused by
organo-chlorine residues). Because
current population sizes and
distribution are large and reproduction
has been restored to a level that can
compensate for normal environmental
fluctuations, we do not believe these
natural events threaten the species
throughout all of its range in the
foreseeable future.
Other Habitat Protections
U.S. laws that provide protections to
brown pelican habitat are the Fish and
Wildlife Coordination Act (16 U.S.C.
661 et seq.), which requires equal
consideration and coordination of
wildlife conservation with other water
resource developments, and the Estuary
Protection Act (16 U.S.C. 1221 et seq.),
which requires Federal agencies to
assess impacts of commercial and
industrial developments on estuaries.
Section 10 of the Rivers and Harbors Act
(33 U.S.C. 401 et seq.) regulates the
building of any wharfs, piers, jetties,
and other structures and the excavation
or fill within navigable water. Sections
402 and 404 of the Federal Water
Pollution Control Act (33 U.S.C. 1251 et
seq.), as amended by the Clean Water
Act (91 Stat. 1566) and the Water
Quality Improvement Act (101 Stat. 7),
provide for the development of
comprehensive programs for water
pollution control and efficient and
coordinated action to minimize damage
from oil discharges.
Additional environmental laws that
help protect pelican habitat and food
sources include: Emergency Wetlands
Resources Act of 1986 (16 U.S.C. 3901
et seq.), which authorizes the purchase
of wetlands from Land & Water
Conservation Fund monies; North
American Wetlands Conservation Act of
1989 (16 U.S.C. 4401 et seq.) which
provides funding for wetland
conservation programs in Canada,
Mexico, and the United States;
Anadromous Fish Conservation Act of
1965 (16 U.S.C. 757a et seq.), which
provides funds for conservation,
development, and enhancement of
anadromous fish (marine fish that breed
in fresh water) through cooperation with
States and other non-Federal interests;
Coastal Barrier Resources Act (16 U.S.C.
3501 et seq.), as amended by the Coastal
Barrier Improvement Act of 1990, which
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encourages conservation of hurricaneprone, biologically rich coastal barrier
islands by restricting Federal
expenditures that encourage
development of coastal barrier islands,
such as providing National Flood
Insurance; Coastal Zone Management
Act of 1972 (16 U.S.C. 1451 et seq.),
which provides fiscal incentives for the
protection, restoration, or enhancement
of existing coastal wetlands or creating
new coastal wetlands and assessing the
cumulative effects of coastal
development on coastal wetlands and
fishery resources; Shore Protection Act
of 1988 (33 U.S.C. 2601 et seq.); Outer
Continental Shelf Lands Act of 1954, as
amended in 1978 and 1985 (43 U.S.C.
1301 et seq.); National Ocean Pollution
Planning Act of 1978 (33 U.S.C. 1701 et
seq.); Oil Pollution Act of 1990 (33
U.S.C. 2701 et seq.); Act to Prevent
Pollution From Ships of 1980 (33 U.S.C.
1901 et seq.); Marine Pollution and
Research and Control Act of 1989;
Ocean Dumping Ban Act of 1988 (33
U.S.C. 1401 et seq.); Marine Protection,
Research, and Sanctuaries Act of 1988
(Pub. L. 100–688); and Federal
Insecticide, Fungicide, and Rodenticide
Act of 1996 (7 U.S.C. 136 et seq.). These
laws and regulations, taken collectively,
help ensure the conservation of brown
pelicans and their habitat.
Climate Change
The Intergovernmental Panel on
Climate Change (IPCC) concluded that
warming of the climate system is
unequivocal (IPCC 2007a, p. 30).
Numerous long-term changes have been
observed including changes in arctic
temperatures and ice, widespread
changes in precipitation amounts, ocean
salinity, wind patterns and aspects of
extreme weather including droughts,
heavy precipitation, heat waves and the
intensity of tropical cyclones (IPCC
2007b, p. 7). Species that are dependent
on specialized habitat types, limited in
distribution, or occurring already at the
extreme periphery of their range will be
most susceptible to the impacts of
climate change. Such species would
currently be found at high elevations,
extreme northern/southern latitudes, or
dependent on delicate ecological
interactions, or sensitive to nonnative
competitors. The brown pelican does
not meet the profile of a species most
susceptible to climate change. It is a
wide-ranging species and is relatively
general in its habitat selection as it is
able to breed in a variety of coastal
habitat types and feed on a variety of
prey items. It is likely that the range of
the species may shift and population
centers may redistribute, but effects of
climate change would not be expected
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to result in significant rangewide
declines in the foreseeable future, based
on information currently available.
In summary, conservation efforts are
continuing to positively affect brown
pelicans, resulting in an overall
rangewide recovery. Although loss of
nesting habitat has occurred on a local
scale, for instance in Puerto Rico
(Collazo et al. 1998, p. 63) and Mexico
(Anderson et al. 2003, p. 1099), we have
no evidence that nesting habitat loss is
limiting pelican populations on a
regional or global scale. While localized
nesting habitat is lost to storms and
erosion, particularly in the Gulf of
Mexico (McNease and Perry 1998, p. 9),
birds have been found to colonize in
other natural areas (Hess and Durham
2002, p. 7) and on manmade islands
(Hess and Linscombe 2006, pp. 3, 6;
Harris 2006). The only area where we
have determined roost sites to be
limited is in southern California, but
this has not had any known impacts to
the population. Much of the U.S. brown
pelican roosting habitat is within
protected areas. We have no evidence to
suggest that commercial fishing in the
United States and elsewhere is limiting
brown pelican populations by reducing
the species’ fish prey base and
regulatory mechanisms are in place
within the United States to manage
fisheries to ensure adequate prey base
˜
for sea birds and other species. El Ninos
and severe freezes may impact brown
pelicans on a short-term, localized basis,
but these events do not pose a
significant threat to the species.
Although some local factors continue to
affect brown pelicans, these factors are
not of sufficient magnitude to affect any
brown pelican populations. Therefore,
we believe that the present or
threatened destruction, modification, or
curtailment of the brown pelican’s
habitat or range is not a significant
factor affecting the brown pelican
throughout all of its range, both now
and for the foreseeable future.
B. Overutilization for Commercial,
Recreational, Scientific, or Educational
Purposes
We are not aware of any
overutilization for commercial,
recreational, scientific, or educational
uses of brown pelicans, although within
the United States, Canada, and Mexico,
the brown pelican is protected from any
such threats. In 1936, the Protection of
Migratory Birds and Game Mammals
Treaty was signed by the United States,
Canada, Japan, Russia, and Mexico (50
Stat. 1311; TS 912), which adopted a
system for the protection of certain
migratory birds, including the brown
pelican, in the United States and
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Mexico. This Treaty provides for
protection from shooting and egg
collection by establishment of closed
seasons and refuge zones.
Implementation of the treaty in the
United States was accomplished by
amending the Migratory Bird Treaty Act
(MBTA) (16 U.S.C. 703 et seq.). The
MBTA and its implementing regulations
(50 CFR parts 20 and 21) prohibit take,
possession, import, export, transport,
selling, purchase, barter, or offering for
sale, purchase, or barter, any migratory
bird, their eggs, parts, and nests, except
as authorized under a valid permit, and
require that such use not adversely
affect populations (50 CFR 21.11). The
MBTA and its implementing regulations
will adequately protect against
overutilization of pelicans within the
United States, Canada, and Mexico (see
discussion of the MBTA in ‘‘Effects of
this Rule’’ section below). Another
Federal law that will continue to offer
some form of protection for the brown
pelican is the Lacey Act (16 U.S.C.
3371–3378), which helps the United
States and other foreign countries
enforce their wildlife conservation laws
by prohibiting trade in wildlife, fish,
and plants that have been illegally
taken, possessed, transported, or sold in
violation of other federal, state, and
foreign laws protecting wildlife.
We do not have any information to
indicate that overutilization for
commercial, recreational, scientific, or
educational uses is occurring now or
will occur in the future. Therefore, we
do not believe overutilization is a
significant factor affecting the brown
pelican throughout all of its range, both
now and in the foreseeable future.
C. Disease or Predation
Several diseases have been identified
as causing illness and mortality of
brown pelicans. The diatom Pseudonitzchia australis (an algae) occasionally
blooms in large numbers off the
California coast and produces the toxin
domoic acid that occasionally causes
mortalities in pelicans (USGS 2002a, p.
5). Erysipelas, caused by the bacterium
Erysipelothrix rhusiopathiae, caused
mortality of about 350 pelicans off the
coast of California during the winter of
1987–1988 (Shields 2002, p. 32). This
outbreak was thought to have been
caused by unusually warm waters
combined with a large number of
pelicans in that area. Avian botulism,
caused by the bacterium Clostridium
botulinum, has caused illness and
mortality of pelicans at the Sonny Bono
Salton Sea National Wildlife Refuge
(USGS 2002b, p. 6). None of these
disease outbreaks have had known longterm impacts on the population, and
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because occurrences are few and selflimiting, we do not believe impacts from
these diseases will become a threat to
brown pelicans throughout all of their
range in the foreseeable future.
West Nile virus is listed on the Center
for Disease Control’s West Nile Virus
Web page (https://www.cdc.gov/westnile)
as causing the mortality of white
pelicans (Pelecanus erythrorhynchos),
the only other species of pelican native
to North America. However, according
to this same Web site and the USGS, no
brown pelican deaths due to West Nile
virus have been reported, although
antibodies for the virus have been found
in captive brown pelicans (USGS 2003a,
p. 6). We do not believe impacts from
West Nile virus will become a threat to
brown pelicans throughout all of their
range in the foreseeable future, since
there is no evidence to date that it
negatively impacts pelicans. The postdelisting monitoring plan will be
designed to detect declines in brown
pelican populations that might arise
from a variety of threats, including West
Nile virus. There is an extensive
network of Federal and State wildlife
agencies and other cooperators that
monitor colonial nesting waterbird
species, including the brown pelican
(see ‘‘Post-Delisting Monitoring Plan’’
section below).
Similar to West Nile virus, avian
influenza, also known as bird flu, is not
currently impacting brown pelicans, but
may be a threat in the future. The term
avian influenza refers to multiple strains
of the influenza virus carried by birds.
Just as with the variety of strains of
human influenza virus, the avian
influenza viral strains differ in strength,
transmission rates, and effects. Strains
of avian influenza known as low
pathanogenic avian influenza (LPAI) are
commonly carried in the intestines of
wild birds and generally do not result in
sick or dead birds (CDC 2006, p. 1).
However, if domesticated birds come
into contact with a LPAI, the viral strain
can mutate to a highly pathanogenic
avian influenza (HPAI), which can
result in significant illness and death
(USGS 2006, p. 2). The mutated HPAI
strain can be secondarily transmitted
back to wild birds in addition to a
variety of other species, including
humans. Currently, the HPAI strain of
avian influenza is not known to occur
in the range of the brown pelican (USGS
2009). It is possible that the HPAI strain
could be carried into the range of the
brown pelican through human travel,
importation of tainted materials, and
migratory birds coming in from affected
areas (USGS 2005, p. 2). At this time,
avian influenza is not impacting brown
pelicans and it is not known how
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populations would respond to exposure.
Multiple government and international
agencies are monitoring the progress of
the disease (see, for example, USDA’s
BioSecurity for Birds at https://
www.aphis.usda.gov/animal_health/
birdbiosecurity). These avian influenza
specific monitoring programs, in
addition to our own post-delisting
monitoring plan, are designed to detect
declines in brown pelicans and other
bird populations that might arise from
threats such as avian influenza in the
future.
Ticks have been implicated as the
cause of nest abandonment on both a
Texas and Peruvian island (King et al.
1977b, p. 1; Duffy 1983a, p. 112).
However, these events were localized
and apparently have had no long-term
impact on population levels in these
areas. Mites and liver flukes have also
been reported in brown pelicans (50 FR
4942; February 4, 1985), but have not
been noted to cause significant health
impairment in healthy birds. We have
no evidence that mites, liver flukes, or
other parasites are limiting brown
pelican populations now or are likely to
in the future. Therefore, we do not
believe impacts from parasites will
become a threat to brown pelicans
throughout all of their range in the
foreseeable future.
Brown pelicans require nesting areas
in close proximity to food supplies and
free from mammalian predators and
human disturbance (Anderson and
Keith 1980, p. 65). There is no known
significant impact from mammalian
predation on brown pelicans,
particularly since they generally nest at
sites free of mammals that could
depredate eggs or young. Mammalian
predators introduced to seabird nesting
islands, such as domestic cats (Felis
catus) and rats (Rattus spp.), can have
serious impacts on small and mediumsized seabirds, but they appear to have
little impact on pelicans (Anderson et
al. 1989, p. 102). However, in some
areas we anticipate that the brown
pelican will benefit from feral cat
removal programs. The Montrose
Trustee Council is planning to remove
the feral cats from San Nicolas Island,
a known brown pelican roosting
location off the southern California
coast, starting in 2009 (Service 2009b).
There are numerous reported avian
predators of chicks and eggs:
magnificent frigatebirds (Fregata
magnificens), gulls (Larus spp.), redtailed hawks (Buteo jamaicensis),
peregrine falcons (Falco peregrinus),
American kestrels (Falco sparverius),
short-eared owls (Asio flammeus), cattle
egrets (Bulbulcus ibis), night herons
(Nycticorax spp.), American
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oystercatchers (Haematopus palliatus),
crows (Corvus spp.), and mockingbirds
(Mimus gilvus) (Schreiber 1979, p. 40;
Saliva and Burger 1989, p. 695; Jiminez
2004, pp. 16–17). Avian predators
occasionally destroy unguarded pelican
nests, and disturbances to nesting
colonies may flush pelicans from nests,
increasing the risk of predation on eggs
and young (Schreiber and Riseborough
1972, p. 126). However, if brown
pelicans are undisturbed, at least one
member of the breeding pair usually
remains close to the nest to protect the
eggs and vulnerable nestlings (Duffy
1983a, p. 113; Schreiber and
Riseborough 1972, p. 126; Shields 2002,
p. 12). In the absence of other human
disturbances, egg and nest predation by
mammals and other birds does not
appear to impose a significant limitation
on brown pelican reproduction. Most
nesting islands are protected from
human disturbance as discussed above.
Therefore, we do not believe impacts
from mammalian or avian predation
will become a threat to brown pelicans
throughout all of their range within the
foreseeable future.
Disease and predation generally affect
only small numbers of individuals. In
addition, many disease events are
usually limited in area and may only
affect brown pelicans for a short period
of time (e.g., for a single breeding
season). Because brown pelicans are
long lived, sporadic breeding failures
that may be caused by parasites, disease,
or predation, especially on a local scale,
have little effect on long-term
population stability (Shields 2002, p.
23). Because current populations and
distribution are large and reproduction
has been restored to a level that can
compensate for normal environmental
fluctuations, we do not believe that
disease, parasites, and predation are a
significant factor affecting brown
pelicans throughout the species’ range,
both now and in the foreseeable future.
D. The Inadequacy of Existing
Regulatory Mechanisms
As discussed in each of the factors,
many regulatory mechanisms will
remain in place after delisting that
ensure future threats will be reduced or
minimized. We believe these
protections, taken together, provide
adequate regulatory mechanisms to
prevent the brown pelican from
becoming endangered throughout all of
its range in the foreseeable future.
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diving into ice-covered water. However,
severe freeze events in Louisiana are
infrequent (McNease et al. 1994, p. 10)
Natural Factors
and have not precluded the Louisiana
This discussion addresses direct
population from growing to large
mortality of brown pelicans. See Factor
numbers since the restocking program
A for impacts to habitat from natural
began in the 1960s.
weather events such as storms and El
Winter storms and severe freezes may
˜
˜
Nino. Weather events and El Nino
locally impact pelicans. For example,
events may affect habitat and prey
larger than usual numbers of pelicans
abundance as discussed above, but also
began washing up on beaches in
may result directly in death or injury of
California during the winter of 2008–
individual brown pelicans. Boersma
2009. This die-off of 300 to 400 birds
˜
(1978, p. 1482) reported El Nino-season
appears to have occurred as a result of
starvation of nestling brown pelicans in a winter storm event in the Pacific
the Galapagos Islands. The 1982–83,
Northwest and weather-related stress in
˜
1986–87, and 1991–1994 El Nino events the northernmost portion of the winter
may have reduced the number of
range of the species where pelicans had
nesting brown pelicans in those years at remained late in the year due to
Cayo Conejo, Puerto Rico (Schreiber
relatively mild weather (California
1999, p. 12). In extreme cases adult
Department of Fish and Game 2009, pp.
˜
mortality has resulted from El Nino
7–8).
events (Shields 2002, p. 32), such as the
These natural factors may adversely
˜
especially severe El Nino (Southern
affect brown pelicans on a short-term,
Oscillation) of 1983 (Duffy 1986, p.
localized basis, but do not pose a
591). Mortality was not noted during the rangewide threat to the continued
less severe event of 1978 (Boersma 1978, existence of the species. These factors
p. 1482). Shields (2002, p. 23, and
generally affect only a limited number
reference cited within) states that food
of individuals, affect only a localized
˜
shortages as a result of El Nino and
area, or affect reproductive success for
other climatic and oceanographic events a single season. The pelican is a longmay result in abandonment of nests and lived species that has evolved with
starvation of nestlings, but rarely results natural phenomena such as variation in
in adult mortality except in extreme
food resources, winter storms, and
events. Because brown pelicans are long hurricanes. These factors are only
lived, such sporadic and short-term
significant when population sizes are
breeding failures have little impact on
small and reproduction is limited.
long-term population viability.
Because current populations and
Storms accompanied by severe tidal
distribution are large and reproduction
flooding can have a significant negative
has been restored to a level that can
effect on brown pelican productivity
compensate for normal environmental
(McNease et al. 1994, p. 10). While some fluctuations, we do not believe that
adults may be killed during storm
natural events will endanger the species
events, most impacts result in juvenile
throughout all of its range in the
mortality and reduced fledgling
foreseeable future.
production (Wilkinson et al. 1994, p.
Manmade Factors
425; Hess and Linscombe 2006, p. 4).
Human disturbance of nesting
Additionally, eggs and nestlings may be
pelicans. Adverse effects on nesting
lost due to flooding (Hess and
pelicans from human disturbance by
Linscombe 2006, p. 23) and nests built
recreationists, scientists, educational
in trees are easily dislodged and
groups, and fishermen have been well
destroyed during strong winds or major
documented (Anderson 1988, p. 342;
storms (Jiminez 2004, pp. 12–17; Saliva
Anderson and Keith 1980, pp. 68–69).
1989). While McNease et al.’s (1994, p.
10) observations indicated a female that Disturbance at nesting colonies, such as
walking among or near nests, has been
has produced eggs or nestlings will not
nest again in the same season, Hess and shown to adversely affect reproductive
success of pelicans, and even result in
Linscombe (2006, pp. 3, 7, 23) found
abandonment of nests or entire colonies
pelicans rebuilding new nests on top of
(Anderson and Keith 1980, p. 69).
flooded and damaged nests.
Collier et al. (2003, pp. 112–113) offer
In addition to freezes in Louisiana
human disturbance as the cause of a
limiting brown pelican foraging and
suspension of breeding activity in a
resulting in fish mortality, as discussed
brown pelican colony on St. Martin in
above under Factor A, McNease et al.
the Lesser Antilles. The colony was near
(1994, p. 10) found effects from severe
a resort with heavy boat and jet ski use.
freezes included high initial brown
When a jet ski passed within about
pelican mortality from hypothermia,
400 m (1,312 ft) of a colony, 40 pelicans
prolonged exposure to low
flushed, leaving their nests unattended
temperatures, and death while plunge-
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and unprotected from predators, but
none flushed when a slow-moving dive
boat approached within 10 m (33 ft) of
the colony.
In Puerto Rico and the U.S. Virgin
Islands, most breeding colonies of
brown pelicans are located within
Commonwealth or Federal protected
areas. The adverse effects of human
disturbances by recreational vessels and
fishermen have been suggested as
potentially resulting in abandonment of
pelican nests located at low elevations
´
and close to the water (Jimenez 2004,
pp. 12–17). Pelicans have been seen
flushing from nests when boats
approached within 152.4 m (500 ft), and
have been noted to leave their nests
unattended for as long as humans
remained within this proximity (Saliva
1996a; Saliva 2003). Raffaele et al.
(1998, pp. 224–225) summarized
historical records of pelicans nesting in
Puerto Rico and noted their extirpation
from at least three colonies and suggests
boat traffic as the cause. Schreiber
(1999, p. 20) noted that one of these
extirpated colonies may have moved to
a nearby bay, hidden from boaters.
Along Mexico’s Pacific Coast, human
disturbance at colonies has resulted in
nest abandonment, predation of eggs
and chicks, and total abandonment or
relocation of individual colonies
(Anderson and Keith 1980, p. 69).
Fishermen, birders, photographers,
educational groups, and egg collectors
(in past years) have occasionally
disturbed the pelican colonies at critical
times during the breeding season (Gress
et al. 2005, p. 7). However, nesting
brown pelicans are monitored annually
as an indicator species in the Gulf of
California (Godinez et al. 2004, p. 48),
and although annual numbers fluctuate
widely due to a number of factors,
including disturbances at some
colonies, the populations are considered
stable (Everett and Anderson 1991, p.
133; Anderson and Palacios 2005, p. 2).
Although the threat of human
disturbance has declined in Mexico as
a result of conservation efforts and
increased protection (Luckenbach
Trustee Council 2006, p. 82),
enforcement remains limited (Anderson
et al. 2003, pp. 1103–1104) and many
colonies are still susceptible to
disturbances (Godinez 2006). However,
effects from disturbance have not been
substantial enough to result in
documented population declines in the
last 20 years (Anderson et al. 2004, p.
37). Therefore, while these local impacts
are still occurring, we do not believe
they currently threaten brown pelicans
or will become a threat that endangers
the brown pelican throughout all of its
range in the foreseeable future.
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Future conservation actions in Mexico
that are not a factor in our rule to delist
the brown pelican, but that would
benefit brown pelicans and reduce
human disturbance if implemented, are
the restoration of seabird colonies on
five pelican nesting islands along the
Pacific Coast of Baja California as part
of the Luckenbach Restoration Plan and
the Montrose Settlements Restoration
Program (MSRP) (Luckenbach Trustee
Council 2006, pp. 74–82, 100, 106;
MSRP 2005, pp. D5–11–12). Proposed
restoration activities include reducing
sources of disturbance at colonies by
redesigning paths and walkways to
manage human traffic, shielding light
sources, and performing public outreach
and education (Luckenbach Trustee
Council 2006, pp. 20, 77).
While human disturbance can cause
brown pelicans to flush from their nests,
there are also situations where the birds
have become habituated to nearby
intense uses (for example, aircraft
activity) without obvious effects on
breeding efforts (Schreiber et al. 1981, p.
398). We believe the current protections
provided by regulatory mechanisms
other than the Endangered Species Act
for nest sites in the United States and to
prevent human disturbances to U.S.
nesting colonies will adequately
continue to protect brown pelicans
throughout their range within the
United States. Additionally, while
human disturbance to brown pelican
nesting colonies is still occurring
outside of the United States, most of the
countries in the species’ range are
protecting, and are expected to continue
to protect, brown pelicans through
implementation of restoration plans,
designated biosphere reserves and
parks, and land ownership and
protection by conservation
organizations and local, State, and
Federal governments (see above for
discussion of nesting habitat
protections). These protections are
implemented through various
mechanisms that do not rely on the U.S.
Endangered Species Act and therefore
are expected to continue if the brown
pelican is delisted. The current levels of
human disturbance are not sufficient to
cause population declines of brown
pelicans, because brown pelicans may
become habituated to some level of
disturbance, may shift nesting locations
(as indicated above in discussion of loss
of nesting habitat), or may only
experience a temporary loss of
reproduction, such as for a single
breeding season. While human
disturbance of brown pelican colonies is
continuing, we do not believe the level
of disturbance is currently sufficient to
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result in population declines of brown
pelicans throughout all of the species’
range in the foreseeable future.
Pesticides and Contaminants. During
initial recovery planning for brown
pelicans, it was recognized that
organochlorine pesticides were the
major threat to the brown pelican in the
United States and these pesticides acted
by direct toxicity (affecting all age
classes) and by impairing reproduction
(reducing recruitment into the
population) (Hickey and Anderson
1968, p. 272; Risebrough et al. 1971, pp.
8–9; Blus et al. 1979b, p. 183).
Impairment of reproduction was
attributed to a physiological response to
the presence of high levels of the
organochlorine
dichlorodiphenyldichloroethylene
(DDE) (Hickey and Anderson 1968, p.
272). DDE is the principal metabolite of
DDT, a synthetic organochlorine
compound that was widely used as a
commercial and agricultural pesticide
from the 1950s through the early 1970s
(Risebrough 1986, p. 401; 37 FR 13369;
July 7, 1972). Brown pelicans gradually
accumulated these toxins by eating
contaminated prey (Hickey and
Anderson 1968, p. 271). DDE interferes
with calcium deposition during eggshell
formation, resulting in the production of
thin-shelled eggs that are easily crushed
during incubation (Gress 1995, p. 10).
DDE also causes the death of embryos in
the egg, and the death or aberrant
behavior of recently hatched young
(Blus 1982, p. 26). The primary reason
for severe declines in the brown pelican
population in the United States was
DDT contamination in the 1960s and
early 1970s.
In California, ocean sediments off the
coast of Los Angeles were heavily
contaminated with DDT residues from a
DDT manufacturing facility that
discharged waste into the sewage
system, which entered the marine
environment through a submarine
outfall (Gress 1995, p. 10). This input
ceased in 1970, after which DDT and
DDE residues in the marine
environment decreased sharply, and
pelican reproductive success improved
as eggshell thickness increased (Gress
1995, p. 10; Gress and Lewis 1988, p.
13). Reproductive declines are thought
to occur when pelican eggshells average
15 to 20 percent thinner than normal
(Gress 1994, p. 7). Mean eggshell
thickness from 1986 to 1990 was only
4.6 percent thinner than the pre-1947
mean, a level which may contribute to
lowered fledging rates in some birds,
but is no longer causing populationwide reproductive impairment in brown
pelicans (Gress 1995, p. 92).
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DDE was also found to be detrimental
to the reproductive success of brown
pelicans in both Texas and Louisiana
(King et al. 1977a, p. 423) and was the
direct cause of brown pelican deaths in
Louisiana (Holm et al. 2003, p. 431).
Since banning of the use of DDT, levels
of DDE residues have declined. The
level of DDE residues in eggs collected
in Texas from 1975 to 1981 was about
one half the level found in eggs
collected in 1970 (King et al. 1985, p.
205; King et al. 1977a, p. 423).
In 1997, Mexico introduced a plan to
strictly curtail and then phase out use
of DDT by 2007 (Environmental Health
Perspectives 1997, p. 1). Mexico used
DDT for control of malaria until 1999
´
(Salazar-Garcıa et al. 2004, p. 542), and
then eliminated its use by 2000, several
years ahead of schedule (Gonzalez 2005,
p. 1). Recent contaminants studies in
the Gulf of California, Mexico, indicate
that this area remains one of the least
contaminated with persistent organic
pollutants in western North America
(Anderson and Palacios 2005, p. 8).
Eggs were collected during the
periods 1980 to 1982 and 1992 to 1993
in Puerto Rico and the U.S. Virgin
Islands (Collazo et al. 1998, pp. 62–63).
Concentrations of DDE and
polychlorinated biphenyls (PCBs) were
significantly higher in the Puerto Rico
eggs than the U.S. Virgin Island eggs
collected in the 1980s. However,
Collazo et al. (1998, p. 64) state that
brown pelican reproduction has not
been affected by contaminants in Puerto
Rico and the U.S. Virgin Islands at least
since the 1980s. Additionally,
contaminant concentrations in the eggs
collected in the 1990s were significantly
lower than those collected in the 1980s
(USGS 2002b, p. 5).
The Environmental Protection Agency
(EPA) banned the use of DDT in the
United States in 1972 (37 FR 13369),
and Canada’s National Office of
Pollution Prevention banned its use in
1985 (Canada Gazette 2005, p. 1). The
Stockholm Convention on Persistent
Organic Pollutants (https://
chm.pops.int/) eliminated or reduced
the use of 12 persistent organic
pollutants, including DDT, in all
participating countries in 2001. All
countries within the breeding range of
the brown pelican are participants. In
addition to the United States and
Canada, Cuba and Costa Rica have
banned its use; Belize, Columbia,
Mexico, and Venezuela have restricted
its use; and eight countries limited
access in other ways (https://
www.pesticideinfo.org). Although lowlevel DDE contamination will probably
persist for many years in areas where
DDT was used, the impact to pelican
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populations is now believed to be
negligible and is expected to continue to
lessen over time. Because regulatory
mechanisms are in place to ban or
strictly limit use of DDT, and current
levels of DDE contamination are no
longer causing population-wide
reproductive impairment in brown
pelicans, DDT or DDE will not endanger
the brown pelican throughout all of its
range within the foreseeable future.
A number of other organochlorine
pesticides have also been documented
to have affected brown pelicans in some
portions of their range. The
organochlorine pesticide endrin is the
probable cause of the brown pelican’s
rapid decline and subsequent
disappearance in Louisiana (King et al.
1977a, p. 427). Endrin was first used in
the Mississippi River Basin in 1952. In
1958, dead fish were reported near
sugarcane fields where endrin was used,
and die-offs of fish and other wildlife
began to consistently occur when heavy
rains produced runoffs from those fields
(King et al. 1977a, p. 427). King et al.
(1977a, p. 427) reported an estimated six
million menhaden found dead between
1960 and 1963. Extensive fish kills
persisted in the lower Mississippi River
and other streams in sugarcane growing
parishes of Louisiana through 1964
(King et al. 1977a, p. 427). It was
concluded that endrin from both
agricultural and industrial sources was
responsible for the fish kills (King et al.
1977a, p. 427). Fish-eating ducks, such
as mergansers, were also reported
floating dead in streams and bayous
(King et al. 1977a, p. 427).
According to Winn (1975, p. 127), the
adverse impact of endrin on brown
pelicans was demonstrated when more
than 300 of the 465 birds introduced to
Louisiana since 1968 died during April
and May 1975. Brain tissue from five
dead pelicans was analyzed. Chemists at
Louisiana State University identified
seven pesticides in the brain tissue, all
chlorinated hydrocarbons widely used
in agriculture. Most of the birds
analyzed contained what experts regard
as potentially lethal levels of endrin. In
addition to endrin, residues of six other
organochlorine pesticides (DDE,
dieldrin, toxaphene, benzene
hexachloride, hexachloro-benzene
(HCB), and heptachlor epoxide) were
found (Winn 1975, p. 127). This
significant die-off demonstrated the
vulnerability of brown pelicans to
endrin and emphasized the possible role
of pesticides in the brown pelican’s
decline in the eastern United States.
Endrin is also one of the pesticides
targeted for elimination by the
Stockholm Convention on Persistent
Organic Pollutants (https://
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chm.pops.int/). Although it is not
currently banned in the United States, it
is not registered for use in the United
States or Canada and is banned in
Belize, Colombia, Cuba, and Peru
(https://www.pesticideinfo.org).
Dieldrin (another organochlorine
pesticide) was also detected at levels
considered detrimental to reproductive
success for brown pelicans in the
eastern portion of the United States
(Blus et al. 1974, p. 186; Blus et al.
1975, p. 653; Blus et al. 1979a, p. 132).
There is only slight evidence that
dieldrin thins eggshells, whereas there
is strong evidence indicating that it
adversely affects egg hatching, posthatching survival, and behavior of
young birds (Dahlgren and Linder 1974,
pp. 329–330; Blus 1982, p. 27). The
agricultural use of dieldrin in the
United States ceased in 1970 and it was
discontinued as a termite control in
1987 (Centers for Disease Control and
Prevention 2005, p. 340). From 1975
through 1978, dieldrin residues
collected from brown pelican eggs in
Texas were found at levels that do not
pose a threat to reproductive success
and survival (King et al. 1985, p. 206).
Other organochlorine insecticides,
including chlordane-related
compounds, HCB, and toxaphene, were
rarely detected in brown pelican eggs
collected in Texas from 1975 to 1978
(King et al. 1985, p. 206). PCBs are
chemicals that were used as coolants
and lubricants in transformers,
capacitors, and other electrical
equipment. Due to concern over the
toxicity and persistence of PCBs, they
were banned in the United States in
1978 (43 FR 33918) under authority of
the Toxic Substance Control Act of 1976
(15 U.S.C. 2601 et seq.). Concentrations
of PCBs in brown pelican eggs collected
in Texas declined more than eight-fold
between 1970 and 1981 (King et al.
1985, p. 206), and are now at levels not
believed to be detrimental.
Claims have been made that
organochlorine pesticides are still used
in South and Central America
(NatureServe 2007, p. 2). However, we
are not aware of any reports of
pesticides affecting reproduction
outside of the United States. Nearly
every nation within the range of the
brown pelican has signed the 2001
Stockholm Convention on Persistent
Organic Pollutants (Resource Futures
International 2001, p. 11). Signatories to
the Convention agree to eliminate the
production and use of DDT, endrin,
dieldrin, chlordane, HCB, toxaphene,
and PCBs, as well as other persistent
organic pollutants, with an exemption
for use of DDT for disease vector (an
organism that transmits disease, such as
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mosquitoes) control in accordance with
World Health Organization
recommendations and guidelines and
when alternatives are not available.
Parties exercising this exemption are to
periodically report their use (Resource
Futures International 2001, p. 12). These
reports are listed on the Convention’s
Web site: https://chm.pops.int/. The
evidence we have found indicates that
reproduction in brown pelicans is no
longer affected by the use of persistent
organochlorine pesticides. Regulatory
mechanisms are currently in place to
eliminate or severely restrict their use
such that they do not threaten the
brown pelican throughout all of its
range within the foreseeable future.
While effects from other
environmental contaminants were not
thoroughly known in the 1970s and
1980s, there were indications that some
localized contaminant-related problems
still existed for the brown pelican.
National Wildlife Health Laboratory
records of brown pelican mortality from
1976 to 1983 documented 10 die-off
incidents totaling over 212 birds along
the U.S. Atlantic Coast (Service 2007a,
p. 29). More recently National Wildlife
Health Laboratory records from July
1995 through June 2003 documented 13
incidents of brown pelican mortality for
the continental United States east of the
Rocky Mountains. None of these records
cite problems with heavy metals, and
pesticides were implicated in just one of
these cases (USGS 2003b). Two pelicans
from Florida had moderate brain
acetlycholinesterase activity depression,
an indicator of poisoning from either
organophosphorus or carbamate
pesticides. While these currently
applied, short-lived, non-organochlorine
pesticides may cause occasional
mortality of individual pelicans, they do
not accumulate within the body, nor do
they persist in the environment;
therefore, they are unlikely to result in
widespread reproductive failure like
that caused by the use of organochlorine
pesticides.
In the United States, an important
regulatory mechanism benefitting brown
pelicans is the requirement that
pesticides be registered with the EPA.
Under the authority of the Federal
Insecticide, Fungicide, and Rodenticide
Act, the EPA requires environmental
testing of the effects of all new
pesticides on representative wildlife
species prior to EPA granting a pesticide
registration. The EPA evaluates
pesticides before they can be marketed
and used in the United States to ensure
that they will not pose unreasonable
adverse effects to human health and the
environment. Pesticides that meet this
test are granted a license or
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‘‘registration,’’ which permits their
distribution, sales, and use according to
requirements set by EPA to protect
human health and the environment. The
requirement for evaluation of pesticides
during the registration process would
not be altered if the pelican was delisted
and protection of the Endangered
Species Act were not available.
Efforts to ban and restrict use of
persistent organic pollutants have
reduced the contaminants that are most
likely to cause widespread reproductive
failures, and thus endangerment of the
species. Other contaminants continue to
be detected in some brown pelican
populations, but these are generally
short-lived pesticides or contaminants
and effects have only been noted to
occur on a local scale and affect few
individuals and therefore are unlikely to
have long-term effects on brown pelican
reproduction or numbers. Regulatory
mechanisms within the United States to
evaluate and register pesticides, as well
as the international convention
restricting use of persistent organic
pollutants, ensure that contaminantcaused mortality and widespread
reproductive failures are unlikely to
occur in the future. Therefore, we do not
believe pesticides and contaminants are
a significant factor affecting the brown
pelican throughout all of its range, both
now and for the foreseeable future.
Commercial fishing. Commercial
fishing can have a direct effect on
pelicans through physical injury caused
by trawling gear. In 1998, a number of
live and dead brown pelicans washed
up on the beach at Matagorda Island,
Texas (Sanchez 2007). Many had
obvious wing damage. This incident
coincided with the opening of the
summer shrimp season. A similar
incident in 1999 also coincided with the
summer shrimp season (Sanchez 2007).
It is possible that the young,
inexperienced birds were colliding with
the shrimp net lines while attempting to
feed on the bycatch (unwanted marine
creatures that are caught in the nets
while fishing for another species),
resulting in incidental death.
Commercial fishing may adversely affect
individual brown pelicans on a shortterm, localized basis, but we do not
believe it poses a rangewide threat to
the continued existence of the species.
Therefore, we do not believe this impact
will become a significant factor affecting
the brown pelican throughout all of its
range in the foreseeable future.
Recreational fishing. Recreational
fishing can have a direct effect on
pelicans through physical injury caused
by fishing tackle. Pelicans are
occasionally hooked by people fishing
from piers or boats (Service 1983, p. 62).
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Superficially embedded hooks can often
be removed without damage; however, a
small tear in the mouth pouch can
hinder feeding and cause death from
starvation (Service 1983, p. 63).
Mortality is likely if a hook is
swallowed or if there is substantial
injury during hook removal (Service
1983, p. 63). Pelicans can become
ensnared in monofilament fishing line
which can result in serious injury,
infections from cuts, impaired
movement and flight, inability to feed,
and death (Service 1983, p. 63).
Pelican Harbor Seabird Station, Inc., a
Florida wildlife rehabilitator, reported
that of the 200 pelicans handled in
1982, roughly 71 percent had fishingrelated injuries. Of these, 12 (8.5
percent) died or were permanently
crippled; the remainder were
rehabilitated. Fishing-related injuries
comprised about 35 percent of all
observed mortality (February 4, 1985; 50
FR 4943). Another seabird rehabilitation
group reported treating some 450 brown
pelicans for fish line or hook injuries
over a 4-year period (February 4, 1985;
50 FR 4943). However, this number of
individuals affected is small in
comparison to global population
numbers and is therefore unlikely to
affect long-term population stability.
Mortality from recreational fishing is
thought to be insignificant to overall
population dynamics, although it has
been a significant cause of injury/
mortality to newly fledged pelicans near
colonies in California in the past
(Service 1983, p. 62). Live anchovies
used for bait and chumming (cut or
ground bait dumped into the water to
attract fish to the area where one is
fishing) attract young pelicans, and they
often swallow baited hooks that they
encounter, which become embedded in
bills or pouches (Service 1983, p. 63). In
California, the closure to vessels at
depths of less than 37 m (120 ft)
offshore of West Anacapa Island has
provided physical separation between
fishing boats and the nesting colony,
which has greatly reduced the
likelihood of these interactions (Gress
2006). Several educational pamphlets
have been developed and distributed by
National Oceanic and Atmospheric
Administration-Fisheries, in
conjunction with the Service, NPS, and
CDFG, to inform recreational fishermen
in California about the impacts of hook
and line injuries to pelicans and other
seabirds and give step-by-step
instructions for removing hooks and
fishing lines from entangled birds.
While injuries and deaths from
recreational fishing do occur, we believe
they are accidental and localized, that
they affect only few individuals, and are
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not likely to pose a significant factor
affecting the brown pelican throughout
all of its range, both now and in the
foreseeable future.
Offshore oil and gas development. Oil
spills and chronic oil pollution from oil
tankers and other vessels, offshore oil
platforms, and natural oil seeps
continue to represent a potential source
of injury and mortality to pelicans
(Carter 2003, p. 3). The effects of oil on
pelicans persist beyond immediate
physiological injuries. Survival and
future reproductive success of oiled
pelicans that are rehabilitated and
released are lower than for non-oiled
pelicans (Anderson et al. 1996, p. 715).
Injury and mortality of large numbers of
pelicans would likely result if a
significant oil spill occurred near a
nesting colony during the breeding
season or near traditional roost sites.
Oil spills from oil tankers and other
vessels are far more common than spills
from oil platforms (Carter 2003, p. 3).
Since 1984, twelve major oil spillrelated seabird mortality events
occurred along the coast of California,
all of which may have adversely
affected breeding, roosting, or migrating
pelicans (Hampton et al. 2003, p. 30).
Only one of these events was from an
offshore oil platform; the rest were from
tankers, oil barges, or non-tanker vessels
(Hampton et al. 2003, p. 30). As an
example, on February 7, 1990, the oil
tanker vessel American Trader ran
aground at Huntington Beach,
California, and spilled 1.6 million liters
(416,598 gallons) of Alaskan crude oil
(American Trader Trustee Council 2001,
p. 1). An estimated 195 pelicans died as
a result of the spill, and 725 to 1,000
oiled pelicans were observed roosting in
the Long Beach Breakwater after the
spill (American Trader Trustee Council
2001, p. 10). The spill occurred just
before the start of the breeding season as
the birds gathered at traditional roosts
before moving to breeding islands,
making large numbers of birds
vulnerable to the oil (American Trader
Trustee Council 2001, p. 10).
Along the United States coastline,
National Marine Sanctuary regulations
prohibit vessels, including oil tankers,
from operating within 1.85 km (1.15 mi)
of any of the Channel or Farallon
islands or in the Monterey Bay or
Olympic Coast sanctuaries (15 CFR
922). In the event of a major oil spill,
this is probably an insufficient distance
from the pelican nesting colonies to
prevent impacts. Vessels frequently pass
through the SCB in established shipping
lanes that are within 5 km (3 mi) of
Anacapa Island to the north and within
50 km (31 mi) to the south (Carter et al.
2000, p. 436). A traffic separation
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scheme north of Anacapa Island in the
Santa Barbara Channel separates
opposing flows of vessel traffic. The
shipping lanes and traffic separation
scheme in the SCB reduces the
likelihood of spills because it reduces
the probability of vessel-to-vessel and
vessel-to platform collisions. Shipping
traffic is increasing offshore of
California, and this may result in
increased oil spills and pollution events
(McCrary et al. 2003, p. 48). There is
also a shipping lane that passes within
25 km (16 mi) of Los Coronados Islands
in Mexico (Carter et al. 2000, p. 436).
However, because impacts of tanker
spills are localized and occur
infrequently, we expect that brown
pelicans will be affected only within
localized areas in the event of spills and
that individual birds will only be
affected infrequently. Therefore, we do
not believe this impact is a significant
factor affecting the brown pelican
throughout all of its range, both now
and in the foreseeable future.
There are 27 offshore oil platforms
and 6 artificial oil and gas islands off
the coast of southern and central
California (McCrary et al. 2003, p. 43).
There are no platforms within the
Channel Islands National Marine
Sanctuary (McCrary et al. 2003, p. 44),
and oil and gas exploration and
development are prohibited within this
Sanctuary, excluding a few oil and gas
leases that existed prior to its
designation. Oil and gas exploration and
development are prohibited in the other
three National Marine Sanctuaries,
Olympic Coast (Washington), Gulf of the
Farallones (California), and Monterey
Bay (California) (15 CFR 922), with the
exception of a few leases that existed
prior to each sanctuary’s creation,
although new petroleum operations are
unlikely to occur on these leases
(McCrary et al. 2003, p. 45). The
sanctuaries essentially provide a minor
buffer from oil platform accidents,
allowing time for breakup of oil
discharges, and time to respond before
the oil reaches the shore. The last major
spill from any of the oil platforms or
associated pipelines was a well blowout
in 1969 that released 80,000 barrels in
the Santa Barbara Channel. The
Minerals Management Service (MMS)
estimates the risk of a spill of 1,000
barrels or more over the next 28 years
at 41 percent (McCrary et al. 2003, p.
45). However, the likelihood that a spill
would affect brown pelicans would
depend on the location, timing, and
local conditions associated with the
spill. Past spills from oil platforms have
not limited brown pelican recovery in
California.
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In the Gulf of Mexico, the Outer
Continental Shelf (OCS) is categorized
into planning areas. The Central
Planning Area includes Louisiana and
Mississippi, and the Western Planning
Area includes Texas (Ji et al. 2002, p.
19). Based on sheer volume of oil
transported to those facilities, coastal
birds and their habitats in these areas
are at greatest risk from spills
originating in coastal waters. An MMS
Oil Spill Risk Analysis (OSRA)
predicted that in these Planning Areas
large oil spills associated with OCS
activities are low-probability events
(Service 2003b, p. 7). The OSRA
estimated only a 4 to 8 percent
probability that an oil spill in the Gulf
of Mexico greater than 1,000 barrels of
oil would occur and contact brown
pelican habitat in the Central Planning
Area, and a similar spill scenario has
only a 4 to 7 percent probability of
reaching the Western Planning Area (Ji
et al. 2002, pp. 56, 59). Estimates
derived from the OSRA model are
‘‘conservative’’ in that they presume the
persistence of the entire volume of
spilled oil over the entire duration time
and do not include cleanup activities or
natural weathering of the spill (Ji et al.
2002, pp. 12–13).
Beginning in the 1980s, MMS
established comprehensive pollution
prevention requirements that include
redundant safety systems, along with
inspecting and testing requirements to
confirm that those devices are working
properly (Service 2003b, p. 7). There
was an 89 percent decline in the volume
of oil spilled per billion barrels
produced from OCS operations between
1980 and the present, compared to the
total volume spilled prior to 1980.
Additionally, this spill reduction
volume occurred during a period when
OCS oil production has been increasing
(Service 2003b, p. 7). Spills less than
1,000 barrels are not expected to persist
as a slick on the water surface beyond
a few days (Service 2003b, p. 8).
Because spills in the OCS would occur
at least 3 miles from shore, it is unlikely
that any spills would make landfall
prior to breaking up (Service 2003b, p.
8).
There are a number of regulatory
mechanisms within the United States
that address oil and gas operations.
MMS is also responsible for inspection
and monitoring of OCS oil and gas
operations (McCrary et al. 2003, p. 46).
All owners and operators of oil
handling, storage, or transportation
facilities located seaward of the
coastline must submit an Oil Spill
Response Plan to the MMS for approval
(30 CFR 254). Several Federal and State
laws were instituted in the 1970s to
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59467
reduce oil pollution (Carter 2003, p. 2).
In 1990, State and Federal oil pollution
acts were passed, and agencies
developed programs to gather data on
seabird mortality from oil spills,
improve seabird rehabilitation
programs, and develop restoration
projects for seabirds (Carter 2003, p. 2).
There have also been improvements in
oil spill response time, containment,
and cleanup equipment (McCrary et al.
2003, p. 46). In the absence of swift and
effective action by the responsible party
for a spill, the U.S. Coast Guard will
initiate action pursuant to the Oil
Pollution Act of 1990 to control and
clean up a spill offshore under regional
area contingency plans, which have
been developed for this scenario (40
CFR 300 Subpart B). These measures
have not entirely eliminated the
potential for oil spills, but have reduced
the likelihood of spills, thereby
reducing pelican deaths and alleviating
the magnitude of the impacts on
pelicans and other seabirds if a spill
were to occur (Carter 2003, p. 3).
If an oil spill or other hazardous
materials release does occur in the
United States, the Natural Resource
Damage Assessment (NRDA) process is
in place to identify the extent of natural
resource injuries (including injuries to
wildlife), the best methods for restoring
those resources, and the type and
amount of restoration required. The
Comprehensive Environmental
Response, Compensation, and Liability
Act of 1980, as amended (42 U.S.C. 9601
et seq.), the Oil Pollution Act of 1990
(33 U.S.C. 2701), and the Federal Water
Pollution Control Act or Clean Water
Act, as amended (33 U.S.C. 1251 et seq.)
form the legal foundation for the NRDA
Restoration Program and provide
trustees with the legal authority to carry
out Restoration Program
responsibilities. Trustees for natural
resources include the Departments of
Agriculture, Commerce, Energy, and the
Interior, and other agencies authorized
to manage or protect natural resources
(EPA 2007a, EPA 2007b, Department of
the Interior 2007). Therefore, if an oil
spill occurs and brown pelicans are
negatively affected, injuries to brown
pelican populations or their habitat may
be restored through this process. For
example, in California, negative effects
to brown pelicans have been mitigated
through the implementation of
restoration measures in the American
Trader Restoration Plan, the Command
Oil Spill Restoration Plan, the Torch/
Platform Irene Restoration Plan, and the
Montrose Settlement Restoration Plan.
Oil spills from oilfields, pipelines, or
ships have impacted brown pelicans in
some other countries. For example,
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oiling related to an oilfield in Mexico
(King et al. 1985, p. 208; Anderson et al.
1996, p. 211) and from a ship in the
Galapagos Islands, Ecuador (Lougheed
et al. 2002, p. 5) affected brown
pelicans. Although 117 brown pelicans
were reported as affected by the 2001
spill in the Galapagos Islands from the
fuel tanker Jessica, no mortalities of
pelicans were reported (Lougheed et al.
2002, p. 29). From these accounts,
brown pelicans frequently survive these
incidences, especially when receiving
some rescue cleanup. Oil spills have
been identified as a possibility in oilproducing areas of Venezuela, with
concern for effects on marine
productivity and the food supply of
brown pelicans, as well as for direct
oiling of birds (Service 2007a, p. 39).
While spills outside of the United States
are still a possibility, they would be
localized and thus would not become a
threat that would endanger the brown
pelican throughout all of its range in the
foreseeable future. In addition, there are
a number of international conventions
and their amendments, including the
International Convention on Civil
Liability for Oil Pollution Damage,
International Convention on Oil
Pollution Preparedness Response and
Co-operation, International Convention
Relating to Intervention on the High
Seas in Cases of Oil Pollution
Casualties, and the International
Convention on the Establishment of an
International Fund of Compensation for
Oil Pollution Damage. The majority of
countries within the range of brown
pelicans are parties to one of more of
these international agreements (https://
sedac.ciesin.org/entri/
treatyMultStatus.jsp), which would
assist with prevention, as well as
response and restoration activities in the
event of oil spills outside the United
States.
Other much less common effects of
offshore oil and gas development have
occasionally been documented. There
have been several instances in Louisiana
of unusual and infrequent mortalities,
generally involving juvenile brown
pelicans, associated with the design and
construction of inshore and offshore oil
platforms (Fuller 2007a, p. 1). Brown
pelicans have been observed strangling
in inshore rig railings and drowning in
uncovered casements (large pipes used
in the drilling process that may fill with
water). The number of brown pelican
mortalities in these incidences was low.
However, through consultation with the
Service, MMS, and the Louisiana
Department of Natural Resources, those
features were modified to virtually
eliminate the problem (Fuller 2007a, p.
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1). Because brown pelicans are also
protected by the MBTA, these
modifications to prevent mortalities are
expected to remain in place after the
protections of the Act are removed.
Oil spills and oil pollution continue
to have potential impacts on brown
pelicans, but spill prevention, response,
and restoration activities have become
more organized and effective, and the
breeding range is large enough that a
single spill, even a major one, would
likely only affect a small fraction of the
population. Additionally, the death of
pelicans from design flaws on platforms
is rare and being remedied. Therefore,
we believe that oil and gas activities,
while they may occasionally have shortterm impacts to local populations, will
not become threats that endanger the
brown pelican throughout all of its
range in the foreseeable future.
Miscellaneous. Within the United
States, brown pelican mortalities have
been documented from electrocution on
power lines and drowning in water
intake pipes. In both cases, through
consultation with the Service, those
features were modified to virtually
eliminate the problem (Fuller 2007b, p.
1). These events were unusual instances
of short-term, localized impacts to
brown pelicans. Continued protection of
brown pelicans under the MBTA will
ensure that future brown pelican
mortality caused by design of man-made
features are similarly addressed.
Conclusion
As required by the Act, we considered
the five threat factors in order to assess
whether the brown pelican is threatened
or endangered throughout all of its
range. When considering the listing
status of the species, the first step in the
analysis is to determine whether the
species is in danger of extinction
throughout all of its range. If this is the
case, then the species is listed as
endangered in its entirety. For instance,
if the threats on a species are acting only
on a portion of its range, but the effects
of the threats are such that they place
the entire species in danger of
extinction, we would list the entire
species.
As discussed above, the primary
reason for severe declines in the brown
pelican population in the United States,
and for designating the species as
endangered, was likely DDT
contamination in the 1960s and early
1970s. Additionally, pesticides like
dieldrin and endrin were also found to
negatively impact brown pelicans. Since
the banning of these organochlorine
pesticides, brown pelican abundance
within the United States has shown a
dramatic recovery, and although annual
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reproductive success varies widely,
populations have remained generally
stable for at least 20 years. The EPA
requires registration and testing of new
pesticides to assess potential impacts on
wildlife, so we do not anticipate that a
pesticide that would adversely affect
brown pelicans will be permitted in the
future. Although DDT contamination
continues to persist in the environment,
based on the nesting population size,
overall population stability, and
improved reproductive success, the
continued existence of brown pelicans
is no longer threatened by exposure to
DDT or its metabolites, and populations
within the United States have recovered
adequately to warrant delisting. We
have no evidence that brown pelicans
outside the United States ever declined
in response to persistent organic
pesticides.
Nesting and roosting colonies in the
United States are expected to continue
to be protected from human disturbance
through local conservation measures,
laws, numerous restoration plans, and
ownership of many of the nesting and
roosting habitats by conservation groups
and local, State, and Federal agencies.
In most countries outside of the United
States where brown pelicans occur,
protection is expected to continue
through implementation of restoration
plans, designated biosphere reserves
and parks, and land ownership by
conservation organizations and local,
State, and Federal governments.
Some nesting and roosting habitat is
expected to continue to be limited at
certain local scales, just as some habitat
destruction is expected to continue.
However, the majority of nesting sites
within the United States and many
outside the United States are protected.
While some nesting habitat may be lost,
it is not likely to be a limiting factor in
brown pelican reproductive success,
since pelicans are broadly distributed
and have the ability to shift breeding
sites in response to changing habitat and
prey abundance conditions. In response
to storms, erosion, and lack of
sedimentation, brown pelicans have
exhibited their dispersal capabilities;
they have established new colonies
elsewhere, and shown an ability to
rebound from low numbers.
Additionally, there are several
restoration activities, such as artificial
island creation and enhancement with
dredge material and barrier island
restoration and protection that will
continue to enhance and protect brown
pelican habitat, particularly within the
U.S. Gulf Coast region.
Impacts from weather events, such as
˜
El Ninos and severe freezes, are also
expected to continue. Natural factors
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such as these may adversely affect
pelican reproduction and survival on a
short-term, localized basis, but alone
pose only a minimal threat to the
species at current population numbers.
Brown pelican prey abundance in the
United States will continue to be
monitored and managed in accordance
with the Magnuson-Stevens Fishery
Conservation and Management Act of
1976. We do not have any information
from outside of the United States on
commercial fishery impacts to brown
pelican prey abundance; however, based
on population numbers, there is no
reason to believe that commercial
fisheries are currently limiting brown
pelican reproductive success.
Brown pelicans are not threatened
with overutilization for commercial,
recreational, scientific, or educational
purposes. Research on pelicans is
generally observational and
noninvasive. Although several diseases
have been identified as a source of
mortality for brown pelicans, they
appear to be self-limiting and sporadic
and are not likely to impact long-term
population trends. Predation is a minor
threat that occurs when disturbance to
nesting colonies leaves eggs and chicks
unprotected, making it essential that
nesting colonies are protected from
disturbance, as noted above.
Commercial and recreational fishing
may adversely affect brown pelicans on
a localized basis, but pose no rangewide
threat to the continued existence of the
species. Oil spills and oil pollution
continue to be a potential threat, but the
breeding range is large enough that a
single spill, even a major one, would
likely only affect a small fraction of the
population. This threat has been
alleviated in the United States to some
degree by stringent regulations for
extraction equipment and procedures,
traffic separation schemes, shipping
lanes that reduce the likelihood of
collisions or spills, and improvements
in oil spill response, containment, and
cleanup. These measures reduce the
probability of spills and also may
reduce adverse impacts if a spill were to
occur.
Foreseeable Future
As discussed above, the brown
pelican continues to be affected by a
variety of localized, short-term impacts.
These localized impacts are generally
expected to continue in perpetuity. For
example, there is no reason to think that
development; hurricanes and other
storm events; random human
disturbance; fishery activities; oil spills;
and infestation by mites, tick, and liver
flukes will not continue at some rate
indefinitely into the future. Because
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these impacts are generally limited to
one breeding season in duration, occur
infrequently, or occur in only a small
portion of the range of the species, they
are not expected to result in declines in
the rangewide status of the species. In
order to reliably predict that these
impacts may result in endangerment in
the foreseeable future, the rate,
magnitude, or intensity of the threats
would have to increase to the point that
population level impacts (e.g., repeated
nesting failures) were seen in at least a
significant portion of the range of the
species. The brown pelican is a longlived species that breeds multiple years
such that sporadic breeding failures
have little effect on long-term
population stability (Shields 2002, p.
23). In many cases, pelicans will
relocate to alternative breeding areas or
pelicans from other areas will
recolonize affected sites. Current
science does not allow us to extrapolate
declines in the species’ status if threats
remain at current levels and further
does not allow us to reliably predict that
these localized, short-term impacts will
change in such a way in the future such
that pelicans will respond negatively
over a significant portion of the range of
the species.
Some diseases such as domoic acid
poisoning, erysipelas, and avian
botulism occur rarely and are subject to
the same fact patterns discussed above
concerning short-term, localized threats.
When considering diseases such as West
Nile virus and avian influenza, it would
not be unexpected for either disease to
move into the range of the brown
pelican; however, the timing, intensity,
and response of pelicans across the
range of the species cannot be reliably
predicted. Thus, the scientific
information does not support these
diseases as threats to the brown pelican
in the foreseeable future.
Predation of chicks and eggs is
occurring at a level low enough to allow
for populations to recover and expand
across the range of the species. This
background level of predation is not
expected to increase or otherwise
change in the future such that this trend
would be reversed as a result of
predation.
The use of pesticides and
contaminants that were known to affect
brown pelicans across the range of the
species has discontinued in most
portions of the range of the species
through implementation of bans, laws,
and treaties. In order to determine that
pesticide and contaminant use may be
a threat to the brown pelican in the
future, its use must not only be
occurring, but be occurring at a level
that impacts the long term population
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59469
levels over at least a significant portion
of the range of the species. Current
scientific and commercial information
simply does not indicate that these two
things are happening or that some
change will occur allowing it to happen
in the future.
The fact that threats are not
considered foreseeable does not mean
that they are not possible, only that
current scientific understanding does
not allow us to reliably predict that
impacts will increase or that a
population decline will result in
response to that impact in the future.
Given current information on threats
and ongoing conservation and
management activities, it would be
speculative to assume that these impacts
will increase to a reliably measureable
level, thus it is not foreseeable that the
threats will impact the species
meaningfully in the future.
In conclusion, the single most
important threat to the continued
existence of the brown pelican was from
DDT, which is now banned in the
United States, Mexico, and Canada. In
Central and South America and the
West Indies, most countries have either
banned or restricted use of DDT or made
its importation illegal (https://
www.pesticideinfo.org/
DetailChemReg.jsp?Rec-Id=PC33482).
Although other localized threats to the
brown pelican remain throughout its
range, as discussed above, they are at a
low enough level that none are likely to
have long-term population level or
demographic effects on brown pelican
populations in the foreseeable future.
We believe this species is no longer in
danger of extinction throughout its
range, nor is it likely to become so in the
foreseeable future.
Significant Portion of the Range
Having determined that the brown
pelican does not meet the definition of
threatened or endangered throughout its
range, we must next consider whether
there are any significant portions of its
range that are in danger of extinction or
are likely to become endangered in the
foreseeable future. On March 16, 2007,
a formal opinion was issued by the
Solicitor of the Department of the
Interior, ‘‘The Meaning of In Danger of
Extinction Throughout All or a
Significant Portion of Its Range’’ (U.S.
Department of the Interior 2007). We
have summarized our interpretation of
that opinion and the underlying
statutory language below. A portion of
a species’ range is significant if it is part
of the current range of the species and
it contributes substantially to the
representation, resiliency, or
redundancy of the species. The
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contribution must be at a level such that
its loss would result in a decrease in the
ability to conserve the species. In other
words, in considering significance, the
Service should ask whether the loss of
this portion likely would eventually
move the species toward extinction, but
not necessarily to the point where the
species should be listed as threatened
throughout its range.
The first step in determining whether
a species is threatened or endangered in
a significant portion of its range is to
identify any portions of the range of the
species that warrant further
consideration. The range of a species
can theoretically be divided into
portions in an infinite number of ways.
However, there is no purpose to
analyzing portions of the range that are
not reasonably likely to be significant
and threatened or endangered. To
identify only those portions that warrant
further consideration, we determine
whether there is substantial information
indicating that (i) the portions may be
significant and (ii) the species may be in
danger of extinction there or likely to
become so within the foreseeable future.
In practice, a key part of this analysis is
whether the threats are geographically
concentrated in some way. If the threats
to the species are essentially uniform
throughout its range, no portion is likely
to warrant further consideration.
Moreover, if any concentration of
threats applies only to portions of the
range that are not significant to the
conservation of the species, such
portions will not warrant further
consideration.
If we identify any portions that
warrant further consideration, we then
determine whether in fact the species is
threatened or endangered in any
significant portion of its range.
Depending on the biology of the species,
its range, and the threats it faces, it may
be more efficient for the Service to
address the significance question first,
or the status question first. Thus, if the
Service determines that a portion of the
range is not significant, the Service need
not determine whether the species is
threatened or endangered there; if the
Service determines that the species is
not threatened or endangered in a
portion of its range, the Service need not
determine if that portion is significant.
The terms ‘‘resiliency,’’
‘‘redundancy,’’ and ‘‘representation’’ are
intended to be indicators of the
conservation value of portions of the
range. Resiliency of a species allows the
species to recover from periodic or
occasional disturbance. A species will
likely be more resilient if large
populations exist in high-quality habitat
that is distributed throughout the range
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of the species in such a way as to
capture the environmental variability
found within the range of the species. It
is likely that the larger size of a
population will help contribute to the
viability of the species overall. Thus, a
portion of the range of a species may
make a meaningful contribution to the
resiliency of the species if the area is
relatively large and contains particularly
high-quality habitat or if its location or
characteristics make it less susceptible
to certain threats than other portions of
the range. When evaluating whether or
how a portion of the range contributes
to resiliency of the species, it may help
to evaluate the historical value of the
portion and how frequently the portion
is used by the species. In addition, the
portion may contribute to resiliency for
other reasons—for instance, it may
contain an important concentration of
certain types of habitat that are
necessary for the species to carry out its
life-history functions, such as breeding,
feeding, migration, dispersal, or
wintering.
Redundancy of populations may be
needed to provide a margin of safety for
the species to withstand catastrophic
events. This does not mean that any
portion that provides redundancy is a
significant portion of the range of a
species. The idea is to conserve enough
areas of the range such that random
perturbations in the system act on only
a few populations. Therefore, each area
must be examined based on whether
that area provides an increment of
redundancy that is important to the
conservation of the species.
Adequate representation insures that
the species’ adaptive capabilities are
conserved. Specifically, the portion
should be evaluated to see how it
contributes to the genetic diversity of
the species. The loss of genetically
based diversity may substantially
reduce the ability of the species to
respond and adapt to future
environmental changes. A peripheral
population may contribute meaningfully
to representation if there is evidence
that it provides genetic diversity due to
its location on the margin of the species’
habitat requirements.
Applying the process described above
for determining whether a species is
threatened in a significant portion of its
range, we next addressed whether any
portions of the range of the brown
pelican warranted further consideration.
We noted in the five-factor analysis that
numerous factors continue to affect
brown pelicans in various geographical
areas within the range. However, we
conclude that these areas do not warrant
further consideration because the areas
where localized effects may still occur
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are small (in the context of the range of
the species) and affect a few pelicans
from one year to the next (such as
abandonment of a single breeding
colony or entanglement in fishing gear),
thus there is no substantial information
that these areas are a significant portion
of the range. Some areas that may be
significant experience short-term or
sporadic events (such as the Gulf Coast
region experiencing tropical storm
events, or Pacific Coast populations
experiencing reduced nesting success
˜
during an El Nino event), but we do not
have substantial information that brown
pelicans in these areas are likely to
become in danger of extinction in the
foreseeable future.
As discussed previously in
Distribution and Population Estimates,
Recovery Plans, and Factors A and E,
declines in wintering numbers of brown
pelicans have been noted in Puerto Rico
(Collazo et al. 2000, p. 40), which
superficially suggest that Puerto Rico
warrants further consideration.
However, Puerto Rico does not
represent a large block of high quality
habitat, is not known to act as a
refugium, and is not known to contain
important concentrations of specialized
habitat types (e.g., breeding, foraging).
As discussed above, brown pelican
populations generally are able to
recolonize neighboring sites that may
have been lost or extirpated during a
catastrophic event (e.g., hurricane). In
this sense, Puerto Rico contributes to
the resiliency of brown pelican
populations; however, all brown pelican
populations contribute to resiliency in
this way and the Puerto Rico
populations are not known to contribute
more significantly to resiliency than
neighboring populations and as such are
considered to have a low contribution to
the resiliency of the species. Because
Puerto Rico represents a small portion
of the range of the species, both
geographically and in total numbers
(240–400 out of 620,000 birds), these
populations have a low contribution to
the redundancy of the species. Finally,
brown pelicans in Puerto Rico belong to
the subspecies of brown pelican
distributed throughout the West Indies
and along the Caribbean coasts of
Colombia and Venezuela and are not
known to contain any unique genetic
materials, morphologies, or behaviors
and thus have a low contribution to the
representation of the species. While it is
important to note that brown pelicans
may serve a vital role in the local flora
and fauna of Puerto Rico and
neighboring areas, these populations are
not significant to the species as a whole
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under the resiliency, redundancy, and
representation framework.
In addition to a determination that the
Puerto Rico populations are not
significant to the conservation of the
species, we did not find that these
populations are in danger of extinction
now or in the foreseeable future. Causes
for the apparent decline in number of
wintering birds are not known and no
specific threats to brown pelicans in
Puerto Rico and the Virgin Islands were
identified in the five factor analysis
above. Although numbers of breeding
pelicans in Puerto Rico and the Virgin
Islands varied from year to year in both
the 1980s and 1990s, there was no trend
in breeding pelican numbers that would
suggest that the species is in danger of
extinction in that area. Nesting sites are
protected from development, human
disturbance of nesting sites is not
known to be limiting, contaminants are
not affecting brown pelican populations
(Collazo et al. 1998, pp. 63–64), and
numbers of nesting pairs appear to be
holding steady (Collazo et al. 2000, p.
42). Juvenile and adult pelicans from
the Virgin Islands disperse to Puerto
Rico (Collazo et al. 1998, p. 63), so
proximity to breeding colonies on the
Virgin Islands and other islands would
likely re-establish the species on Puerto
Rico even if it were lost. In the absence
of identified threats or evidence that
brown pelicans in Puerto Rico represent
a significant portion of the species’
range, we did not consider this portion
of the range further.
INVEMAR (2008) states that pelicans
in Colombia may be impacted by a
variety of factors including port
construction, mangrove deforestation,
development, overfishing, pollution,
disease, and hunting. However, we have
found no information to indicate that
these factors are leading to declines in
numbers of brown pelican in Colombia.
In fact, the seven sites where Moreno
and Bulevas (2005, p. 11) document
brown pelicans to occur in Colombia all
have some form of protection. For
example, the largest population in
Colombia occurs on Isla Gorgona which
is a Parque Nacional Natural, or national
park, and is protected from most
disturbance. Further, similar to the
situation for Puerto Rico, the Colombian
populations of brown pelican do not
appear to be genetically different from
other brown pelicans and this portion of
the range does not appear to include a
concentration of an important specific
habitat type or a large portion of
unusually high quality habitat. In
summary, in our analysis of the five
listing factors, we did not identify any
significant continuing threats in any
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20:34 Nov 16, 2009
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portion of the species range that
warrants further consideration.
In conclusion, major threats to brown
pelicans have been reduced, managed,
or eliminated. Remaining factors that
affect brown pelicans occur on localized
scales, are short-term events, or affect
small numbers of individuals and do
not have long-term effects on population
numbers or distribution of the species.
We have determined that none of the
existing or potential threats, either alone
or in combination with others, are likely
to cause the brown pelican to become in
danger of extinction within the
foreseeable future throughout all or any
significant portion of its range. We
believe the brown pelican no longer
requires the protection of the Act, and,
therefore, we are removing it from the
Federal List of Endangered and
Threatened Wildlife.
Effect of This Rule
This rule revises 50 CFR 17.11(h) to
remove the brown pelican from the List
of Endangered and Threatened Wildlife.
Because no critical habitat was ever
designated for this species, this rule
would not affect 50 CFR 17.95.
The prohibitions and conservation
measures provided by the Act,
particularly through sections 7 and 9, no
longer apply. Federal agencies are no
longer required to consult with us to
ensure that any action they authorize,
fund, or carry out is not likely to
jeopardize the continued existence of
this species. This rulemaking, however,
does not affect the protection given to
all migratory bird species under the
MBTA.
The take of all migratory birds,
including brown pelicans, is governed
by the MBTA. The MBTA makes it
unlawful to at any time, by any means
or in any manner, to pursue, hunt, take,
capture, kill, attempt to take, capture, or
kill, possess, offer for sale, sell, offer to
barter, barter, offer to purchase,
purchase, deliver for shipment, ship,
export, import, cause to be shipped,
exported, or imported, deliver for
transportation, transport or cause to be
transported, carry or cause to be carried,
or receive for shipment, transportation,
carriage, or export, any migratory bird,
any part, nest, or eggs of any such bird,
or any product, whether or not
manufactured, which consists, or is
composed in whole or part, of any such
bird or any part, nest, or egg thereof (16
U.S.C. 703(a)). Brown pelicans are
among the migratory birds protected by
the MBTA. The MBTA regulates the
taking of migratory birds for
educational, scientific, and recreational
purposes. Section 704 of the MBTA
states that the Secretary of the Interior
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59471
(Secretary) is authorized and directed to
determine if, and by what means, the
take of migratory birds should be
allowed, and to adopt suitable
regulations permitting and governing
the take. In adopting regulations, the
Secretary is to consider such factors as
distribution and abundance to ensure
that any take is compatible with the
protection of the species. Modification
to brown pelican habitat would
constitute a violation of the MBTA only
to the extent it directly takes or kills a
brown pelican (such as removing a nest
with chicks present).
Post-Delisting Monitoring Plan
Section 4(g)(1) of the Act requires that
the Secretary, through the Service,
implement a monitoring program for not
less than 5 years for all species that have
been recovered and delisted. The
purpose of this requirement is to
develop a program that detects the
failure of any delisted species to sustain
itself without the protective measures
provided by the Act. If at any time
during the monitoring program, data
indicate that the protective status under
the Act should be reinstated, we can
initiate listing procedures, including, if
appropriate, emergency listing. At the
conclusion of the monitoring period, we
will review all available information to
determine if relisting, the continuation
of monitoring, or the termination of
monitoring is appropriate. We proposed
a draft post-delisting monitoring plan in
the Federal Register on September 30,
2009 (74 FR 50236) and expect to
finalize that post-delisting monitoring
plan within a year.
Paperwork Reduction Act
Office of Management and Budget
(OMB) regulations at 5 CFR part 1320,
which implement provisions of the
Paperwork Reduction Act (44 U.S.C.
3501 et seq.) require that Federal
agencies obtain approval from OMB
before collecting information from the
public. This rule does not contain any
new collections of information that
require approval by OMB under the
Paperwork Reduction Act. This rule will
not impose recordkeeping or reporting
requirements on State or local
governments, individuals, businesses, or
organizations.
National Environmental Policy Act
We have determined that
Environmental Assessments or
Environmental Impact Statements, as
defined under the authority of the
National Environmental Policy Act of
1969, need not be prepared in
connection with actions adopted
pursuant to section 4(a) of the Act. We
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Federal Register / Vol. 74, No. 220 / Tuesday, November 17, 2009 / Rules and Regulations
published a notice outlining our reasons
for this determination in the Federal
Register on October 25, 1983 (48 FR
49244).
References Cited
A complete list of all references we
cited is available upon request from the
Clear Lake Ecological Services Office
(see FOR FURTHER INFORMATION CONTACT).
Authors
jlentini on DSKJ8SOYB1PROD with RULES2
The primary authors of this final rule
are staff members of the Southwest
Regional Office, Albuquerque, New
Mexico.
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List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Regulation Promulgation
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Public Law
99–625, 100 Stat. 3500; unless otherwise
noted.
§ 17.11
[Amended]
■
2. Amend § 17.11(h) by removing the
entry for ‘‘Pelican, brown’’ under BIRDS
from the List of Endangered and
Threatened Wildlife.
PART 17—[AMENDED]
Dated: October 28, 2009.
Christine E. Eustis,
Acting Director, Fish and Wildlife Service.
[FR Doc. E9–27402 Filed 11–16–09; 8:45 am]
■
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations as set forth
below:
1. The authority citation for part 17
continues to read as follows:
■
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BILLING CODE 4310–55–P
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Agencies
[Federal Register Volume 74, Number 220 (Tuesday, November 17, 2009)]
[Rules and Regulations]
[Pages 59444-59472]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-27402]
[[Page 59443]]
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Part III
Department of the Interior
-----------------------------------------------------------------------
Fish and Wildlife Service
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50 CFR 17
Endangered and Threatened Wildlife and Plants; Removal of the Brown
Pelican (Pelecanus occidentalis) From the Federal List of Endangered
and Threatened Wildlife; Final Rule
Federal Register / Vol. 74 , No. 220 / Tuesday, November 17, 2009 /
Rules and Regulations
[[Page 59444]]
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[FWS-R2-ES-2008-0025 ; 92220-1113-0000-C6]
RIN 1018-AV28
Endangered and Threatened Wildlife and Plants; Removal of the
Brown Pelican (Pelecanus occidentalis) From the Federal List of
Endangered and Threatened Wildlife
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: Under the authority of the Endangered Species Act of 1973, as
amended (Act), we, the U.S. Fish and Wildlife Service (Service), are
removing the brown pelican (Pelecanus occidentalis) from the Federal
List of Endangered and Threatened Wildlife due to recovery. This action
is based on a review of the best available scientific and commercial
data, which indicate that the species is no longer in danger of
extinction, or likely to become so within the foreseeable future. The
brown pelican will remain protected under the provisions of the
Migratory Bird Treaty Act.
DATES: The effective date of this rule is December 17, 2009.
ADDRESSES: This final rule is available on the Internet at https://www.regulations.gov and https://www.fws.gov/southwest/es/Library/.
Supporting documentation used in preparing this final rule will be
available for public inspection, by appointment, during normal business
hours, at the Service's Clear Lake Ecological Services Field Office,
17629 El Camino Real 211, Houston, Texas 77058-3051.
FOR FURTHER INFORMATION CONTACT: Steve Parris, Field Supervisor, U.S.
Fish and Wildlife Service, Clear Lake Ecological Services Field Office,
17629 El Camino Real 211, Houston, Texas 77058-3051; telephone
281/286-8282; facsimile 281/488-5882. If you use a telecommunications
device for the deaf (TDD), call the Federal Information Relay Service
(FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Brown pelican (Pelecanus occidentalis) populations currently listed
under the Endangered Species Act of 1973, as amended (Act; 16 U.S.C.
1531 et seq.) occur in primarily coastal marine and estuarine (where
fresh and salt water intermingle) environments along the coast of the
Gulf of Mexico from Mississippi to Texas and the coast of Mexico; along
the Caribbean coast from Mexico south to Venezuela; along the Pacific
Coast from British Columbia, Canada, south through Mexico into Central
and South America; and in the West Indies, and are occasionally sighted
throughout the United States (Shields 2002, pp. 2-4). Brown pelicans
remain in residence throughout the breeding range, but some segments of
many populations migrate annually after breeding (Shields 2002, p. 6).
Overall, the brown pelican continues to occur throughout its historical
range (Shields 2002, pp. 4-5). This rule includes biological and life
history information for the brown pelican relevant to the delisting.
Additional information about the brown pelican's biology and life
history can be found in the Birds of North America, No. 609 (Shields
2002, pp. 1-36).
This rule applies to the entire listed species, which includes all
brown pelican (Pelecanus occidentalis) subspecies. The species
Pelecanus occidentalis is generally recognized as consisting of six
subspecies: (1) P. o. occidentalis (Linnaeus, 1766: West Indies and the
Caribbean Coast of South America, occasionally wanders to coasts of
Mexico and Florida), (2) P. o. carolinensis (Gmelin, 1798: Atlantic and
Gulf coasts of the United States and Mexico; Caribbean Coast of Mexico
south to Venezuela, South America; Pacific Coast from southern Mexico
to northern Peru, South America), (3) P. o. californicus (Ridgeway,
1884: California south to Colima, Mexico, including Gulf of
California), (4) P. o. urinator (Wetmore, 1945: Galapagos Islands), (5)
P. o. murphyi (Wetmore, 1945: Ecuador and Pacific Coast of Colombia),
and (6) P. o. thagus (Molina, 1782: Peru and Chile). Recognition of
brown pelican subspecies is based largely on relative size and color of
plumage and soft parts (for example, the bill, legs, and feet). The
distributional limits of the brown pelican subspecies are poorly known,
so the geographic descriptions of their ranges are approximate and may
not be adequate to assign subspecies designations. Additionally, some
authors elevate the Peruvian subspecies to a separate species, Peruvian
pelican (P. thagus) (see Remsen et al. 2009). However, the taxonomy of
the brown pelican subspecies has not been critically reviewed for many
years, and the classification followed by the American Ornithologists'
Union (American Ornithologists' Union 1957, pp. 29-30) and by Palmer
(1962, pp. 274-276) is based on Wetmore's (1945, pp. 577-586) review,
which was based on few specimens from a limited portion of the range.
Remsen et al. (2009) does not present a comprehensive taxonomic
treatment of all brown pelicans, but rather, relies on already noted
morphological differences to propose that P. o. thagus be recognized as
a full species. Additional taxonomic review of all brown pelicans would
be needed to further elucidate the relationships and distributions of
the six described subspecies. The original listing of the brown pelican
included the species throughout its range and covered all six of the
subspecies described above. This rule continues that taxonomic
treatment, including the Peruvian brown pelican (P. o. thagus).
Previous Federal Actions
On February 20, 2008, we published a 12-month petition finding and
proposed rule to remove the brown pelican from the Federal List of
Endangered and Threatened Wildlife (73 FR 9408). We solicited data and
comments from the public on the proposed rule. The comment period
opened on February 20, 2008, and closed on April 21, 2008. Note that
this proposed rule addresses the status of brown pelicans throughout
their range except where previously delisted along the Atlantic Coast
of the United States, in Florida, and in Alabama (50 FR 4938; February
4, 1985). For more information on previous Federal actions concerning
the brown pelican, please refer to the proposed rule published in the
Federal Register on February 20, 2008 (73 FR 9408).
Distribution and Population Estimates
Information on population estimates below is arranged
geographically for convenience and to present a logical organization of
the information. These broad geographic areas do not necessarily
represent populations or other biologically based groupings. The six
subspecies described above are not used to organize the following
information because distributional limits of the subspecies are poorly
known, especially in Central and South America. Additionally, the broad
overlap in wintering and breeding ranges among the subspecies
introduces considerable uncertainty in assigning subspecies
designations in portions of the species range (Shields 2002, p. 5).
Because the brown pelican is a wide-ranging, mobile species, is
migratory throughout much of its range, and may shift its breeding or
wintering areas or distribution in response to local
[[Page 59445]]
conditions, it is difficult to define local populations of the species.
Much of the population estimate information below is given at the scale
of individual countries, which may not correspond with actual
biological populations, particularly for smaller countries that may
represent only a fraction of the species' range. Direct comparison of
all the estimates provided below is difficult because methods used to
derive population estimates are not always reported, some population
estimates are given as broad ranges, and some do not specify whether
the estimates are for breeding birds or include nonbreeding birds as
well. However, the information does indicate the broad distribution of
the species and reflects the large global population estimate of more
than 620,000 birds, which does not include previously delisted birds
along the Atlantic coast of the United States, in Florida, or in
Alabama (Service 2007a, pp. 44-45).
Gulf of Mexico Coast
Mississippi.--Turcotte and Watts (1999, pp. 84-86) consider the
brown pelican a permanent resident of the Mississippi coast, even
though there are no records of nesting brown pelicans in Mississippi.
Brown pelicans are currently not known to breed in Mississippi, but the
annual Christmas Bird Counts have documented wintering brown pelicans
in Mississippi since 1985 (National Audubon Society 2009, pp. 1-3). The
most recent counts over the winter of 2008-2009 sighted 372 brown
pelicans (National Audubon Society 2009, p. 3).
Louisiana.--Before 1920, brown pelicans were estimated to have
numbered between 50,000 and 85,000 in Louisiana (King et al. 1977a, pp.
417, 419). By 1963, the brown pelican had completely disappeared from
Louisiana (Williams and Martin 1968, p. 130). A reintroduction program
was conducted between 1968 and 1980. During this period, 1,276 nestling
brown pelicans were transplanted from colonies in Florida to coastal
Louisiana (McNease et al. 1984, p. 169). After the initiation of the
reintroduction, the population reached a total number of 16,405
successful nests and 34,641 young produced in 2001 (Holm et al. 2003,
p. 432).
In 2003, the number of nesting colonies increased, but numbers of
successful nests decreased to 13,044 due to four severe storms that
eroded portions of some nest islands and destroyed some late nests in
various colonies (Hess and Linscombe 2003, Table 2). According to
surveys conducted by the Louisiana Department of Wildlife and Fisheries
(LDWF), the population appeared to recover from these impacts and a
peak of 16,501 successful nests producing 39,021 fledglings was
recorded in 2004 (LDWF 2006, p. 1; Hess and Linscombe 2006, p. 13).
However, tropical storms in 2004 resulted in the loss of three nesting
islands east of the Mississippi River and, after storm events in late
2005, LDWF surveys detected 25,289 fledglings (Hess and Linscombe 2006,
p. 13). Surveys in 2006 detected 8,036 successful nests in 15 colonies,
producing 17,566 fledglings with an average of 2.1 fledglings per
successful nest (Hess and Linscombe 2007, pp. 1, 4). In 2007, there
were 14 colonies that produced 24,085 fledglings with an average of 2.2
fledglings per nest (LDWF 2008, pp. 3, 6).
Hess and Linscombe (2007, p. 4) concluded that the brown pelican
population in Louisiana is maintaining sustained growth despite lower
fledgling production in 2005 and 2006 (a decrease of 31 percent from
2005 to 2006). Fledgling production has increased 37.1 percent from
2006 to 2007 (LDWF 2008, p. 5). Numbers of successful nests are not
directly comparable to numbers of individuals in historic estimates
because they do not account for immature or nonbreeding individuals or
provide an index of population size in years when breeding success is
low due to factors such as weather and food availability. However,
numbers of successful nests and fledglings produced annually since 1993
(Hess and Linscombe 2007, p. 4; LDWF 2008, p. 4) do indicate continued
nesting and successful fledging of young sufficient to sustain a viable
population in Louisiana. See ``Storm effects, weather, and erosion
impacts to habitat'' under Factor A for further discussion of effects
of storms.
Texas.--Brown pelicans historically numbered around 5,000 in Texas
but began to decline in the 1920s and 1930s, presumably due to shooting
and destruction of nests (King et al. 1977a, p. 419). According to King
et al. (1977a, p. 422), there were no reports of brown pelicans nesting
in Texas in 1964 or 1966. There were two known nesting attempts in
1965, but the success of these nests is not known. Annual aerial and
ground surveys of traditional nesting colonies conducted in Texas
during the period 1967 to 1974 indicated that only two to seven pairs
attempted to breed in each of these years. Only 40 young were
documented fledging during this entire 8-year period (King et al.
1977a, p. 422).
The Texas Colonial Waterbird Census has tracked population trends
in Texas for the brown pelican since 1973 (Service 2006, p. 5).
Although the Texas population of brown pelicans did not experience the
total reproductive failure recorded in Louisiana, the first year (1973)
of information from the Texas census identified only one nesting colony
with six breeding pairs in the State. Since that time, there was a
gradual increase through 1993 when there were 530 breeding pairs in two
nesting colonies; in 1994, there was a substantial increase to 1,751
breeding pairs in three nesting colonies (Service 2006, pp. 3-5). Since
then, the overall increasing trend has continued with some year-to-year
variation (Service 2006, pp. 2-3). The most recent complete count of
breeding birds in Texas occurred in 2008 and reported 6,136 pairs
(Service 2009c). This number equates to 12,272 breeding birds, which is
substantially greater than historical population estimates for Texas.
Gulf Coast of Mexico.--Very little information is available about
the status of the brown pelican along the Gulf Coast in Mexico. Aerial
surveys indicated that brown pelicans in Mexico were virtually absent
as a breeding species along the Gulf of Mexico north of Veracruz by
1968 (Service 1979, p. 10). An aerial survey conducted in March 1986
along this same stretch of coast counted 2,270 birds, down from 4,250
birds estimated in counts conducted between December 1979 and January
1980 (Blankenship 1987, p. 2). However, the counts in 1986 and in 1980
differed in the areas covered and timing of counts and represent only
two data points, so it is difficult to compare the earlier and later
counts. A recent survey of colonial waterbirds at Laguna Madre de
Tamaulipas did not locate brown pelicans (Pronatura and Audubon Texas
2008), although brown pelicans were not sighted there during the 1986
aerial surveys either (Blankenship 1987, Table 1). No other recent
information for this portion of the species' range was found, so no
conclusions on population trends of the brown pelican for the Mexican
portion of the Gulf Coast can be drawn.
Summary of Gulf of Mexico Coast.--Along the U.S. Gulf Coast, brown
pelican populations, while experiencing some periodic or local
declines, have increased dramatically from a point of near
disappearance in the 1960s and 70s. Brown pelicans were present along
the Gulf Coast of Mexico in 1986, but we currently lack recent
information on the status of the species in this portion of its range.
[[Page 59446]]
West Indies
The West Indies refers to a crescent-shaped group of islands
occurring in the Caribbean Sea consisting of the Bahamas, the Greater
Antilles (including Cuba, Jamaica, Haiti, the Dominican Republic, and
Puerto Rico), and the Lesser Antilles (a group of island countries
forming an arc from the U.S. Virgin Islands on its northwest end
southeast to Grenada). Van Halewyn and Norton (1984, p. 201) summarized
the breeding distribution of brown pelicans throughout the Caribbean
region and noted at least 23 sites where the species was reliably
reported nesting in the islands of the West Indies at some time since
1950. Based on the most recent estimates available at the time, van
Halewyn and Norton (1984, p. 201) documented more than 2,000 breeding
pairs throughout the West Indies. More recently, Collazo et al. (2000,
p. 42) estimated the minimum number of brown pelicans throughout the
West Indies at 1,500 breeding pairs, and Bradley and Norton (2009, p.
275) estimated the West Indian population at 1,630 breeding pairs.
Raffaele et al. (1998, pp. 224-225) describe the brown pelican as ``A
common year-round resident in the southern Bahamas, Greater Antilles
and locally in the northern Lesser Antilles east to Montserrat. It is
common to rare through the rest of the West Indies with some birds
wandering between islands.''
In a search for additional seabird breeding colonies in the Lesser
Antilles, Collier et al. (2003, pp. 112-113) did not find brown
pelicans nesting on Anguilla, Saba, and Dominica. In an attempt to
survey seabirds in St. Vincent and the Grenadines, Hayes (2002, p. 51)
found brown pelicans in the central Grenadines. He notes that brown
pelicans were once considered common in the Grenadines and suggests
that a small nesting colony may exist there, although there is no
historical record of nesting.
Anguilla, Montserrat, Jamaica, the Bahamas, and Antigua.--Recent
information presented in Bradley and Norton (2009, p. 275) reports 21
breeding pairs in Anguilla, 14 in Montserrat, greater than 150 in
Jamaica, 50 in the Bahamas, and 53 in Antigua.
St. Maarten.--Collier et al. (2003, p. 113) reported finding two
nesting colonies on St. Maarten Island in 2001, with a total of 64
nesting pairs, but in 2002 found no breeding pelicans at one of the two
sites surveyed in 2001. Reasons for the lack of breeding activity in
2002 are unknown, although Collier et al. (2003, p. 113) suggested a
disturbance event could have been the cause. The May 2006 newsletter
for the Society for the Conservation and Study of Caribbean Birds
(Society for the Conservation and Study of Caribbean Birds 2006) notes
that St. Maarten's proposed Important Bird Areas of Fort Amsterdam and
Pelikan Key host regionally important populations of nesting brown
pelicans, although numbers of nesting birds are not given.
Puerto Rico and U.S. Virgin Islands.--Collazo et al. (1998, pp. 63-
64) compared demographic parameters between 1980-82 and 1992-95 for
brown pelicans in Puerto Rico. The mean number of individuals observed
during winter aerial population surveys between 1980 and 1982 was
2,289, while mean winter counts from 1992 to 1995 averaged only 593
birds (Collazo et al. 1998, p. 63). Reasons for the decrease in number
of wintering birds between the two periods are not known; however,
migrational shifts could have contributed to the decrease in winter
counts between survey periods (Collazo et al. 1998, p. 63). The number
of nests observed at the selected study sites did not show such an
appreciable decline during the same period for Puerto Rico and the
nearby U.S. Virgin Islands, with nest counts ranging from 167 to 250
during 1980 to 1982, compared with 222 and 256 during 1992 to 1993
(Collazo et al. 1998, p. 64). Collazo et al. (2000, p. 42) estimated
approximately 120-200 nesting pairs in Puerto Rico and 300-350 nesting
pairs in the U.S. Virgin Islands. Information provided by Puerto Rico's
Department of Natural and Environmental Resources places population
estimates in the same relative range as Collazo et al. (1998) with an
average of 437 individuals found in aerial surveys conducted from 1996
to 2004 (Department of Natural and Environmental Resources 2008, pp. 1,
3), although it is not known if these were summer or winter surveys.
Additionally, the U.S. Virgin Islands' Department of Planning and
Natural Resources reports that about 300 nesting pairs have been
counted in the U.S. Virgin Islands annually (Department of Planning and
Natural Resources 2008, p. 1), a comparable number to that reported by
Collazo et al. (1998). Finally, more recent information from Bradley
and Norton (2009, p. 275) reports 265 breeding pairs in Puerto Rico and
325 breeding pairs in the U.S. Virgin Islands.
Cuba.--Acosta-Cruz and Mugica-Vald[eacute]s (2006, pp. 10, 65)
reported that brown pelicans are a common resident species, with the
population augmented by migrants during the winter. Brown pelicans have
been documented nesting at five sites in the Archipi[eacute]lago
Sabana-Camag[uuml]ey and in the Refugio de Fauna R[iacute]o
M[aacute]ximo (Acosta-Cruz and Mugica-Vald[eacute]s 2006, pp. 32-33).
The number of nesting pairs at Refugio de Fauna R[iacute]o
M[aacute]ximo was estimated at 16 to 36 pairs during monitoring in 2001
and 2002 (Acosta-Cruz and Mugica-Vald[eacute]s 2006, p. 33). No
estimates were given for other nesting sites. More recent data from
Bradley and Norton (2009, p. 275) estimates there to be 300 nesting
pairs in 18 colonies in Cuba.
Aruba.--Information provided by Veterinary Service of Aruba, the
country's Convention on International Trade in Endangered Species of
Wild Fauna and Flora (CITES; 27 U.S.T. 1087) Management Authority,
estimates the breeding population on the island to be 20 pairs with a
total population estimate of 60 individuals (Veterinary Service of
Aruba 2008, p. 1).
Summary of West Indies.--Although we do not have detailed
information on brown pelicans throughout all of the islands of the West
Indies, the distribution and abundance of current breeding colonies
reported by Collazo et al. (2000, p. 42), van Halewyn and Norton (1984,
pp. 174-175, 201), and Bradley and Norton (2009, p. 275) are all
similar and in the range of 1,500 to 2,000 breeding pairs.
Caribbean and Atlantic Coasts of Mexico, Central America, and South
America
No comprehensive population estimates for the Caribbean and
Atlantic Coasts of Central and South America are available to our
knowledge, although some estimates for other portions of the species'
range include birds that nest on the mainland coast or offshore islands
(e.g., van Halewyn and Norton's estimate of 6,200 pairs in the
Caribbean included birds nesting on the mainland and offshore islands
of Colombia and Venezuela (1984, p. 201)).
Mexico.--Isla Contoy Reserva Especial de la Biosfera off the coast
of Cancun, Quintana Roo, Mexico, was the site of Mexico's largest brown
pelican nesting colony in 1986, with 300 nesting pairs (Blankenship
1987, p. 2). By the spring of 1996, 700 to 1,000 pairs of brown
pelicans were estimated to be nesting on Isla Contoy (Shields 2002, p.
35). Four other colonies in this region accounted for 128 nesting pairs
in 1986 (Blankenship 1987, p. 2).
Belize.--Miller and Miller (2006, pp. 7, 64) analyzed Christmas
Bird Count data collected in Belize from 1969-2005 and reported that
brown pelican numbers over this period have remained about the same.
References compiled and summarized by Miller and Miller (2006, pp. 144-
149) variously report
[[Page 59447]]
brown pelicans as: ``Common: high density, likely to be seen many
places,'' ``Transient, present briefly as migrant,'' ``Resident,
species present all year,'' and ``apparently secure in Belize.'' Brown
pelicans are also reported in one reference as nesting on several cays
(small, low islands composed largely of coral or sand), but no
information on number of nesting birds or locations are given.
Guatemala.--Brown pelicans in Guatemala are considered to be a
breeding resident (Eisermann 2006, p. 55), although locations of
nesting sites and number of breeding pairs are not given. Eisermann
(2006, p. 65) estimated the Caribbean slope population of brown
pelicans in Guatemala to consist of approximately 376 birds.
Honduras.--Thorn et al. (2006, p. 29) report brown pelicans nesting
on the Caribbean coast of Honduras and offshore islands. Brown pelicans
are reported as a common resident in Honduras, with numbers estimated
to range between 10,000 and 25,000 birds and a stable population trend
(Thorn et al. 2006, p. 20).
Nicaragua.--Zolotoff-Pallais and Lezama (2006, p. 74) report that
the number of brown pelicans within Nicaragua falls within the range
1001-5000 and is stable, although they do not indicate whether this
estimate represents only breeding birds.
Costa Rica.--Brown pelicans are considered a resident species in
Costa Rica, but are not reported nesting on the Caribbean coast of
Costa Rica (Quesada 2006, pp. 9, 46).
Panama.--Brown pelicans primarily nest in the Gulf of Panama on the
Pacific coast with no nesting reported on the Caribbean coast (Angehr
2005, pp. 15-16). However, brown pelicans do winter along the Caribbean
coast of Panama. In 1993, 582 brown pelicans were counted in Panama
(Shields 2002, p. 22) along the Caribbean coast, and Angehr (2005, p.
79) considers brown pelicans to be a ``fairly common migrant'' along
the Caribbean coast.
Colombia.--Moreno and Buelvas (2005, p. 57) report that brown
pelicans occur at four sites on the Caribbean coast of Colombia, with a
good population of brown pelicans in the coastal wetlands of La
Guajira. However, no estimate of numbers of breeding birds was given.
Information provided by Colombia's Instituto de Investigaciones Marinas
y Costeras (INVEMAR) report approximately 20 breeding pairs on the
Caribbean coast of Colombia with additional migratory birds present
(INVEMAR 2008).
Venezuela.--Based on aerial surveys of the Venezuelan coast, Guzman
and Schreiber (1987, p. 278) estimated a population size of 17,000
brown pelicans in 25 colonies. Within those breeding colonies, 3,369
nests were counted (Guzman and Schreiber 1987, p. 278). More recently,
Rodner (2006, p. 9) confirms that there are approximately 25 brown
pelican colonies in Venezuela. Rodner (2006, p. 9) does not give an
overall estimate of the brown pelican population in Venezuela but notes
more than 1,700 nests have been documented in four of the largest
breeding colonies, while another recent census of four sites resulted
in counts of 2,097 pelicans.
South of Venezuela, brown pelicans are reported as a nonbreeding
migrant in Guyana (Johnson 2006, p. 5), French Guiana (Delelis and
Pracontal 2006, p. 57), Surinam (Haverschmidt 1949, p. 77; Ottema 2006,
p. 3), and Brazil (De Luca et al. 2006, pp. 3, 40)
Summary of the Caribbean/Atlantic Coast.--In general, brown
pelicans are broadly distributed on the Caribbean and Atlantic coasts
of southern Mexico and Central and South America and are still present
throughout their historic range with population numbers likely in the
range of 30,000 to 50,000 birds, based on the numbers presented above.
California and Pacific Coast of Northern Mexico
The most recent population estimate of the brown pelican subspecies
that ranges from California to Mexico along the Pacific Coast is
approximately 70,680 nesting pairs, which equates to 141,360 breeding
birds (Anderson et al. 2007, p. 8). They nest in four distinct
geographic areas: (1) The Southern California Bight (SCB), which
includes southern California and northern Baja California, Mexico; (2)
southwest Baja California; (3) the Gulf of California, which includes
coastlines of both Baja California and Sonora, Mexico; and (4) mainland
Mexico further south along the Pacific coastline (including Sinaloa and
Nayarit) (Service 1983, p. 8).
During the late 1960s and early 1970s, the SCB population declined
to fewer than 1,000 pairs and reproductive success was nearly zero
(Anderson et al. 1975, p. 807). In 2006, approximately 11,695 breeding
pairs were documented at 10 locations in the SCB: 3 locations on
Anacapa Island, 1 on Prince Island, and 1 on Santa Barbara Island in
California; 3 on Los Coronados Islands, 1 on Islas Todos Santos, and 1
on Isla San Mart[iacute]n in Mexico within the SCB (Henny and Anderson
2007, p. 9; Gress 2007). In 2007, brown pelicans in California nested
on west Anacapa Island and Santa Barbara Island but did not nest on
Prince Island (Burkett et al. 2007, p. 8). The populations on Todos
Santos and San Mart[iacute]n islands were previously extirpated in 1923
and 1974, respectively; however, these were recently found to be
occupied (Gress et al. 2005, pp. 20-25). Todos Santos Island had about
65 nests in 2004, but there were no nests in 2005. This colony is
currently considered to be ephemeral, occurring some years and then not
others (Gress et al. 2005, p. 28). At San Mart[iacute]n Island, 35
pairs were reported in 1999, a small colony was noted in 2000, and 125-
200 pairs were seen in 2002, 2003, and 2004 (Gress et al. 2005, pp. 20-
25).
The southwest Baja California coastal population has about 3,100
breeding pairs, the Gulf of California population is estimated at
43,350 breeding pairs, and the mainland Mexico populations (including
islands) is estimated to have 12,385 breeding pairs (Anderson et al.
2007, p. 8). The Gulf of California population remained essentially the
same from 1970 to 1988 (Everett and Anderson 1991, p. 125). It is
thought that populations in Mexico have been stable since the early
1970s (when long-term studies began) because of their lower exposure to
organochlorine pesticides (e.g., DDT), although annual numbers at
individual colonies fluctuate widely due to prey availability and human
disturbance at colonies (Everett and Anderson 1991, p. 133).
Summary of California and Pacific Coast of Northern Mexico.--Henny
and Anderson (2007, pp. 1, 8) concluded that their preliminary
estimates of nesting pairs in 2006 suggest a large and healthy total
breeding population for California and the Pacific coast of Mexico.
Pacific Coast of Central America and South America
As with the Caribbean and Atlantic coasts of Central and South
America, there are no comprehensive population estimates for brown
pelicans along this portion of their range.
Guatemala, El Salvador, Honduras, and Nicaragua.--Brown pelicans
are considered a nonbreeding visitor on the Pacific slope of Guatemala
(Eisermann 2006, p. 4) with an estimated abundance of 2,118 birds.
About 800 brown pelicans are widely distributed along the Pacific Coast
of El Salvador (Ibarra Portillo 2006, p. 2). However, Herrera et al.
(2006, p. 44) reported brown pelicans to be a nonbreeding visitor in El
Salvador with numbers falling within the range 1,001-10,000 and an
increasing trend. Brown pelicans occur on the Pacific Coast of Honduras
but are not reported to nest there (Thorn et al. 2006, p. 26, 29).
Zolotoff-Pallais and Lezama (2006, p. 74) report that the
[[Page 59448]]
number of brown pelicans within Nicaragua falls within the range 1,001-
5,000, but do not indicate locations or breeding status.
Costa Rica.--The Costa Rican Ministry for Environment and Energy
has reported that several breeding colonies exist on the Pacific Coast
from the Nicaraguan border to the Gulf of Nicoya and include the
islands of Bolanos and Guayabo (Service 2007a, p. 13). Shields (2002,
p. 35) estimated as many as 850 pairs in Costa Rica. However, Quesada
(2006, p. 37) estimated the brown pelican population in Costa Rica to
fall within the range 10,000-25,000 birds with a stable population
trend.
Panama.--Estimates of brown pelicans in Panama have varied greatly
over the years. In 1981, Batista and Montgomery (1982, p. 70) estimated
that 25,500 adults and chicks were known to occur on just the Pearl
Island Archipelago in the Gulf of Panama. In 1982, Montgomery and
Murcia (1982, p. 69) estimated 70,000 adults occurred at 7 colonies
within the Gulf of Panama. By 1988, 6,031 brown pelicans were known
from just the Gulf, while in 1998, only 3,017 brown pelicans were
thought to occur along the entire Pacific Coast of Panama, including
the Gulf (Shields 2002, p. 22). By 2005, 4,877 brown pelican nests were
reported just in the Gulf of Panama and a total population was
estimated to be about 15,000 individuals for the entire Pacific Coast
of Panama, which includes 150 nests found at Coiba Island in 1976
(Angehr 2005, p. 6). Angehr (2005, p. 12) also reported that those
individual colonies that had been studied experienced an overall
increase of 70 percent in nest numbers from 1979 to 2005, and describes
the brown pelican on the Pacific Coast of Panama as an ``abundant
breeder.''
Colombia.--Moreno and Buelvas (2005, p. 57) list brown pelicans as
occurring at three protected sites on the Pacific coast of Colombia:
Malpelo Island, Gorgona Island, and Sanquianga. Naranjo et al. (2006b,
p. 178) estimated 2,000-4,000 brown pelicans at Sanquianga on the
mainland and 4,800-5,200 on Gorgona Island. Brown pelicans were
considered to be one of the most abundant resident species in a 1996-
1998 assessment of waterbird populations on the Pacific Coast of
Colombia (Naranjo et al. 2006a, p. 181). Naranjo et al. (2006b, p. 179)
concluded that preliminary results of their waterbird monitoring
program on the Pacific coast of Colombia indicate that populations of
Pelecaniformes (which include brown pelicans) in the three protected
areas are stable. INVEMAR (2008) also report approximately 3,000
breeding pairs known from the Pacific coast of Colombia, which
represents approximately 6,000 birds and is consistent with estimates
by Naranjo et al. (2006b).
Ecuador.--On Ecuador's Galapagos Islands, Shields (2002, p. 35)
cites reports of a few thousand pairs. Delaney and Scott (2002, p. 29)
estimated the population on the Galapagos to be 5,000 birds. Santander
et al. (2006, pp. 44, 49) reported that brown pelicans in the Galapagos
number less than 10,000 and are considered common there, while
populations on the mainland range from 25,000 to 100,000. The
Ministerio del Ambiente of Ecuador has reported that nesting brown
pelicans are widely distributed and fairly common along the mainland
coast of that country (Rojas 2006).
Peru.--Shields (2002, p. 22) summarizes estimates of brown pelicans
in Peru at 420,000 adults in 1981-1982, 110,000 in 1982-1983, 620,000
in 1985-1986, and 400,000 in 1996. Franke (2006, p. 10) reported that a
1997 survey of guano birds counted 140,000 brown pelicans with an
increasing population trend reported; however, it is unclear from the
report whether that number represents a total estimate of the brown
pelican population in Peru or a subset of birds nesting on islands
managed for guano production.
Chile.--The range of brown pelicans in Chile extends from the
extreme northern city of Arica (Rodr[iacute]guez 2006) to occasionally
as far south as Isla Chilo[eacute] (Aves de Chile 2006, p. 1). The
total population size for Chile is unknown (Shields 2002, p. 35). The
breeding population on Isla P[aacute]jaro Ni[ntilde]o in central Chile
was 2,699 pairs in 1995-1996, 1,032 pairs in 1996-1997, and none during
the 1997-1998 El Ni[ntilde]o (a temporary oscillation of the ocean-
atmosphere system) year (Simeone and Bernal 2000, p. 453).
Two sightings of brown pelicans in Argentina in 1993 and 1999 are
considered ``hypothetical'' records because they are not documented by
specimens, photographs, or other concrete evidence (Lichtschein 2006).
Summary of Pacific Coast of Central and South America.--Brown
pelicans are abundant breeders along the Pacific coast of Central and
South America with population numbers in the range of 65,000 to 200,000
birds, not including an estimated 400,000 birds in Peru.
Summary--Global Distribution and Population Estimates
As discussed above, currently listed brown pelican populations are
widely distributed throughout the coast of the Gulf of Mexico from
Mississippi to Texas and the coast of Mexico; along the Caribbean coast
from Mexico south to Venezuela; along the Pacific Coast from British
Columbia, Canada, south through Mexico into Central and South America;
and in the West Indies. Population estimates for various States,
regions, and countries reviewed above are not strictly comparable
because they were not made using any standard protocol or methodology,
and in many cases the process by which the estimates were developed is
not described. For example, surveys conducted in different parts of the
year may yield differing results due to migratory trends and breeding
patterns. While in some cases these estimates may be reliable in
describing local abundance and trends, because of their
incomparability, they have limited value in estimating absolute size or
trends in the global population.
During our 5-year status review of the brown pelican, we estimated
the global listed brown pelican population based on the best available
information at the time of the review, which included most but not all
of the individual estimates given above. Although these estimates
represented the best available information at the time of the review,
because of the lack of standardization and major differences in
determining population estimates, we used conservative assumptions in
tabulating these data in order to make a conservative estimate of the
global population size of the brown pelican (see Service 2007a, pp. 43-
45 and 60-62). Specifically, where only numbers of nests are known, the
total number of nests was simply doubled to obtain an estimate of total
population size for an area. This method likely underestimates the
population size because there are likely to be unpaired or immature
nonbreeders in the population. Additionally, where a population
estimate found in the literature was a range of numbers, the lower
number was used in calculating the global estimate. Population size is
merely one factor in determining whether a species is recovered, and
this approach assures we are making our determination in a manner that
is protective of the species.
This total, or global estimate, as given in our 5-year review, is
for the listed brown pelican, which does not include the Atlantic coast
of the United States, Florida, and Alabama. The total based on regional
estimates is over 620,000 individuals, which includes an estimated
400,000 pelicans from Peru (Service 2007a, pp. 43-45 and 60-62). This
is likely a conservative estimate given that estimates for some
countries
[[Page 59449]]
given above (for example, estimates for Colombia and Cuba) were not
readily available at the time we conducted our 5-year review. Other
recent estimates yield similar numbers. Kushlan et al.'s (2002, p. 64)
estimate for the North American Waterbird Conservation Plan area, which
includes Canada, the United States, Mexico, Central America, the
Caribbean, and Caribbean islands of Venezuela, was 191,600-193,700
breeders. Delaney and Scott (2002, p. 29) applied a correction factor
to Kushlan et al.'s estimate to account for immature birds and
nonbreeders to estimate a population of 290,000 birds. Neither estimate
includes birds on the Pacific Coast of South America. Delaney and Scott
(2002, p. 29) additionally estimated the brown pelican population on
the Galapagos to be about 5,000 birds, and the population on the
Pacific Coast of South America (estimate is for the subspecies
Pelecanus occidentalis thagus, found in Peru and Chile) to range from
100,000-1,000,000 birds. Shields' (2002, p. 21) population estimate of
202,600-209,000 brown pelicans also did not include the Peruvian
subspecies. While each of these estimates covers slightly different
areas, they are all in general agreement and indicate that the listed
population of brown pelicans, excluding the Peruvian subspecies, totals
200,000 or more individuals, while the Peruvian subspecies numbers in
the few hundred thousand.
Recovery Plan
Section 4(f) of the Act directs us to develop and implement
recovery plans for listed species. While brown pelicans were listed
throughout their range, recovery planning efforts for the brown pelican
focused primarily on those portions of the species' range within the
United States. We have published three recovery plans for the brown
pelican: (1) Recovery Plan for the Eastern Brown Pelican (Service
1979); (2) the California Brown Pelican Recovery Plan (Service 1983);
and (3) Recovery Plan for the Brown Pelican in Puerto Rico and the U.S.
Virgin Islands (Service 1986).
Section 4(f) of the Act requires the Service to develop and
implement recovery plans for the conservation and survival of
threatened and endangered species, unless we find that such a plan will
not promote the conservation of the species. The Act directs that, to
the maximum extent practicable, we incorporate into each plan: (1)
Site-specific management actions that may be necessary to achieve the
plan's goals for conservation and survival of the species; (2)
objective, measurable criteria, which when met would result in a
determination, in accordance with the provisions of section 4 of the
Act, that the species be removed from the list; and (3) estimates of
the time required and cost to carry out the plan. However, revisions to
the List (adding, removing, or reclassifying a species) must reflect
determinations made in accordance with section 4(a)(1) and 4(b).
Section 4(a)(1) requires that the Secretary determine whether a species
is threatened or endangered (or not) because of one or more of five
threat factors. Therefore, recovery criteria must indicate when a
species is no longer threatened or endangered by any of the five
factors. In other words, objective, measurable criteria, or recovery
criteria, contained in recovery plans must indicate when an analysis of
the five threat factors under 4(a)(1) would result in a determination
that a species is no longer threatened or endangered. Section 4(b)
requires the determination made under section 4(a)(1) as to whether a
species is threatened or endangered because of one or more of the five
factors be based on the best available science.
Thus, while recovery plans are intended to provide guidance to the
Service, States, and other partners on methods of minimizing threats to
listed species and on criteria that may be used to determine when
recovery is achieved, they are not regulatory documents and cannot
substitute for the determinations and promulgation of regulation
required under section 4(a)(1). Determinations to remove a species from
the list made under section 4(a)(1) must be based on the best
scientific and commercial data available at the time of the
determination, regardless of whether that information differs from the
recovery plan.
In the course of implementing conservation actions for a species,
new information is often gained that requires recovery efforts to be
modified accordingly. There are many paths to accomplishing recovery of
a species, and recovery may be achieved without all criteria being
fully met For example, one or more criteria may have been exceeded
while other criteria may not have been accomplished, yet the Service
may judge that, overall, the threats have been minimized sufficiently,
and the species is robust enough, to reclassify the species from
endangered to threatened or perhaps delist the species. In other cases,
recovery opportunities may have been recognized that were not known at
the time the recovery plan was finalized. These opportunities may be
used instead of methods identified in the recovery plan.
Likewise, information on the species may be learned that was not
known at the time the recovery plan was finalized. The new information
may change the extent that criteria need to be met for recognizing
recovery of the species. Overall, recovery of species is a dynamic
process requiring adaptive management, planning, implementing, and
evaluating the degree of recovery of a species that may, or may not,
fully follow the guidance provided in a recovery plan.
Thus, while the recovery plan provides important guidance on the
direction and strategy for recovery, and indicates when a rulemaking
process may be initiated, the determination to remove a species from
the List is ultimately based on an analysis of whether a species is no
longer threatened or endangered. The following discussion provides a
brief review of recovery planning for the brown pelican, as well as an
analysis of the recovery criteria and goals as they relate to
evaluating the status of the species.
The Recovery Plan for the Eastern Brown Pelican, which includes the
Atlantic and Gulf Coasts of the United States, does not identify
recovery criteria because the causes of the species' decline were not
well understood at the time the plan was prepared. The recovery team
viewed the wide distribution of the species, rather than absolute
numbers, as the species' major strength against extinction (Service
1979, p. iv). This recovery plan also addressed brown pelicans in
Alabama, Florida, and the Atlantic Coast of the United States, but
because these populations have already been delisted, we only discuss
the plan's objectives for the portion of the range that remained listed
in Louisiana and Texas.
The recovery plan states a general objective to reestablish brown
pelicans on all historically used nesting sites in Louisiana and Texas
(Service 1979, p. iii). The plan identified 9 sites in Louisiana and 11
sites in Texas. These included historic, current (at the time of the
recovery plan), and restored islands. Since 2005, brown pelicans have
nested at between 11 and 15 sites in Louisiana and at 12 sites in Texas
(Hess and Linscombe 2006, pp. 1-4, 7-8; Service 2006, p. 2). These
sites include some of the same sites identified in the recovery plan as
well as previously unknown or newly colonized sites.
The number and location of nesting sites has varied from year to
year along the Gulf Coast due in part to frequent tropical storms, but
generally meet the recovery plan goals for number of
[[Page 59450]]
nesting sites. The northern Gulf of Mexico coast is subject to frequent
severe tropical storms and hurricanes, which can cause significant
changes to brown pelican nesting habitat. Past storms have resulted in
changes to or loss of historical nesting sites, but brown pelicans seem
well adapted to responding to losses of breeding sites by moving to new
locations (Hess and Durham 2002, p. 7; Wilkinson et al. 1994, p. 425;
Williams and Martin 1968, p. 136), and the species has clearly shown
its ability to rebound (Williams and Martin 1968, p. 130; Holm et al.
2003, p. 432; Hess and Linscombe 2006, pp. 5, 13) (see ``Storm effects,
weather, and erosion impacts to habitat'' under Factor A for further
discussion).
While nesting is not occurring on all historically identified sites
in Texas and Louisiana, the number of currently used nesting sites
meets or exceeds the numbers identified in the recovery plan and
supports sustainable populations of brown pelicans. Because brown
pelicans have demonstrated the ability to move to new breeding
locations when a nesting island is no longer suitable, meeting the
exact number and location of nesting sites in Texas and Louisiana
identified in the recovery plan is not necessary to achieve recovery
for the brown pelican. As discussed further below, we also have
considered the population's wide distribution, numbers, and
productivity as indicators that the threats have been reduced such that
the population is recovered and sustainable.
The Recovery Plan for the Brown Pelican in Puerto Rico and the U.S.
Virgin Islands has delisting criteria solely for the area covered by
the plan. The criteria are to maintain a 5-year observed mean level of:
(1) 2,300 individuals during winter, and (2) 350 breeding pairs at the
peak of the breeding season. Both recovery criteria are solely based on
demographic characteristics and do not provide an explicit reference
point for determining whether threats have been reduced. The levels in
the criteria were based on studies of brown pelicans from 1980 to 1983
(Collazo 1985). Subsequent winter counts from 1992 to 1995 in Puerto
Rico were 74 percent lower than during 1980-1982 (593 individuals
compared to 2,289). Although the 1992 to 1995 counts did not include
the Virgin Islands, it appears likely that the first criterion had not
been met as of 1995 (Collazo et al. 1998). However, reasons for lower
counts are unknown. Collazo et al. (1998, pp. 63-64) concluded that
habitat was not limiting and suggested that migrational shifts could
have contributed to the decrease in numbers and that longer term
monitoring of at least 6 to 8 years is needed to define an acceptable
range of population parameters for brown pelicans in the Caribbean.
Collazo et al. (1998, p. 64) also concluded that contaminants are not
affecting brown pelican reproduction.
Thus, while the first criterion, based on 4 years of data, may not
be sufficient to establish a realistic figure to reflect recovery, it
also does not address whether threats to the species are still present.
Also, because the criterion applies to only a small portion of the
species' range, as well as only a portion of the species' range in the
Caribbean, we do not consider it relevant for determining whether the
brown pelican is recovered globally. Of the two recovery criteria, the
second criterion is the more appropriate to the evaluation of the
status of the species as it reflects population productivity. The
number of pairs seemed to be holding steady between the early 1980s and
the 1990s with estimates given by Collazo et al. (2000, p. 42) of 165
pairs for Puerto Rico and 305-345 pairs for the U.S. Virgin Islands.
While this estimate is not a 5-year observed mean, the estimated number
is consistent with the recovery criterion for number of breeding pairs.
Moreover, data from the U.S. Virgin Islands (Department of Planning and
Natural Resources 2008, p. 1) supports the Collazo et al. (2000, p. 42)
numbers by estimating the brown pelican population there at about 300
breeding pairs.
The California Brown Pelican Recovery Plan only covers the
California brown pelican subspecies (P. o. californicus), which
includes the Pacific Coast of California and Mexico, including the Gulf
of California. The primary objective of this recovery plan is to
restore and maintain stable, self-sustaining populations throughout
this portion of the species' range. To accomplish this objective, the
recovery plan calls for: (1) Maintaining existing populations in
Mexico; (2) assuring long-term protection of adequate food supplies and
essential nesting, roosting, and offshore habitat throughout the
subspecies' range; and (3) restoring population size and productivity
to self-sustaining levels in the SCB at both the Anacapa and Los
Coronados Island colonies. Existing populations appear to be stable in
Mexico and throughout the subspecies range (Everett and Anderson 1991,
p. 133; Henny and Anderson 2007, pp. 1, 8), food supplies are assured
by the Coastal Pelagic Species Fishery Management Plan, and the
majority of essential nesting and roosting habitat throughout the
subspecies' range is protected (see ``Summary of Factors Affecting the
Species'' below for further discussion). Therefore, criteria 1 and 2 of
the recovery plan have been met.
For population and productivity objectives, the recovery plan
included the following additional criterion: (a) When any 5-year mean
productivity for the SCB population reaches at least 0.7 young per
nesting attempt from a breeding population of at least 3,000 pairs, the
subspecies should be considered for reclassification from endangered
status to threatened status; and (b) When any 5-year mean productivity
for the SCB population reaches at least 0.9 young per nesting attempt
from a breeding population of at least 3,000 pairs, the subspecies
should be considered for delisting. Consideration for reclassification
to threatened would require a total production averaging at least 2,100
fledglings per year over any 5-year period. Consideration for delisting
would require a total production averaging at least 2,700 fledglings
per year over any 5-year period.
The criterion, including both productivity and population size, for
downlisting to threatened has been met at least 10 times since 1985.
The delisting population criterion of at least 3,000 breeding pairs has
been exceeded every year since 1985, with the exception of 1990 and
1992, which saw only 2,825 and 1,752 pairs, respectively. In most
years, the nesting population far exceeds the 3,000 pair delisting
goal; it has exceeded 6,000 pairs for 10 of the last 15 years (Gress
2005). Additionally, the delisting criterion of at least 2,700
fledglings per year over any 5-year period has been met at least 11
times since 1985 (Gress 2005). However, although productivity has
improved greatly since the time of listing, the productivity criterion
for delisting has not been met and the SCB population consistently has
low productivity, with a mean of 0.63 young fledged per nesting attempt
from 1985 to 2005 (Gress and Harvey 2004, p. 20; Gress 2005).
Productivity is an important parameter used for evaluating
population health; however, it is difficult to determine an objective
and appropriate minimum value. The 0.9 young per nesting attempt given
in the recovery plan was the best estimate based on a review of brown
pelican reproductive parameters in Florida and the Gulf of California
(Schreiber 1979, p. 1; Anderson and Gress 1983, p. 84), because pre-DDT
productivity for the SCB population was unknown. Despite the fact that
this goal has not been
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reached, reproduction has been sufficient to maintain a stable
population for more than 20 years. Most colonies expanded during this
interval, including the long-term colonization of Santa Barbara Island,
which suggests that productivity has been sufficient to maintain a
stable-to-increasing population. In conclusion, the first two recovery
criteria for the California Brown Pelican Recovery Plan have been met.
As discussed above, the population component of the third criterion has
been far exceeded, while the productivity component has not been met.
We have concluded, based on current population size and productivity,
that the productivity component of the third criterion is no longer
appropriate because current productivity is sufficient to maintain a
viable population of brown pelicans. Please see responses to comments 6
and 8 below for additional discussion of the productivity criterion.
Recovery Planning Summary--The three recovery plans for the brown
pelican discussed above have not been actively used in recent years to
guide recovery of the brown pelican because they are either outdated,
lack recovery criteria for the entire species, or in the case of the
eastern brown pelican, lack recovery criteria altogether. No subsequent
revisions have been made to any of these original recovery plans. No
single recovery plan covers the entire range of the species in the
United States, and the remainder of the range outside the United
States, including Central America, South America, and most of the West
Indies is not covered by a recovery plan. Additionally, the recovery
criteria in these plans do not specifically address the five threat
factors used for listing, reclassifying, or delisting a species as
outlined in section 4(a)(1) of the Act. Consequently, the recovery
plans do not provide an explicit reference point for determining the
appropriate legal status of the brown pelican based either on
alleviating the specific factors that resulted in its initial listing
as an endangered species or on addressing new risk factors that may
have emerged since listing. As noted above, recovery is a dynamic
process and analyzing the degree of recovery requires an adaptive
process that includes not only evaluating recovery goals and criteria
but also new information that has become available. Thus, while some
recovery criteria and many of the goals in the three brown pelican
recovery plans have been met, our evaluation of the status of the brown
pelican in this rule is based largely on the analysis of threats in our
recently completed 5-year review (Service 2007a, pp. 1-66), available
at https://ecos.fws.gov/docs/five_year_review/doc1039.pdf, and
presented below.
Summary of Public and Peer Review Comments and Recommendations
In our February 20, 2008 proposed rule, we requested all interested
parties submit information, data, and comments concerning multiple
aspects of the status of the brown pelican. The comment period was open
from February 20, 2008, through April 21, 2008.
In accordance with our policy on peer review, published on July 1,
1994 (59 FR 34270), we solicited opinions from eight expert scientists
who are familiar with this species regarding pertinent scientific data
and assumptions relating to supportive biological and ecological
information for the proposed rule. Reviewers were asked to review the
proposed rule and the supporting data, to point out any mistakes in our
data or analysis, and to identify any relevant data that we might have
overlooked. Four of the eight peer reviewers submitted comments. Three
of those four were generally supportive of the proposal to remove the
brown pelican from the Federal List of Threatened and Endangered
Species while the fourth reviewer did not offer an opinion. Their
comments are included in the summary below and/or incorporated directly
into this final rule.
During the 60-day comment period, we received comments from 19
individuals, organizations, and government agencies. We have read and
considered all comments received. We updated the rule where it was
appropriate, and we responded to all substantive issues received,
below.
Peer Review Comments
(1) Comment: The inclusion of brown pelicans on the List (Federal
List of Threatened and Endangered Wildlife) has provided us with a
means of protecting habitat that has also protected many other species
that share the marine habitat with the brown pelican. With this
delisting, we will lose protections afforded to all these other marine
species.
Response: When making listing and delisting determinations, we are
only to consider the best scientific and commercial information data in
preparing the five-factor analysis. This analysis has us consider a
variety of impacts to the species in question and the regulatory
mechanisms that may mitigate those impacts, but does not allow us to
consider impacts of listing and delisting on other species. However,
brown pelicans will remain protected by the Migratory Bird Treaty Act
of 1918 (16 U.S.C. 703-711; 40 Stat. 755) and, as discussed below,
numerous other mechanisms confer protections to the brown pelican and
to other species and habitats that are not dependent on the protections
afforded brown pelicans by the Endangered Species Act.
(2) Comment: Multiple commenters expressed concerns over our global
population estimate, specifically noting that the number reached is
vague and speculative because a complete and coordinated survey for the
entire species has never been done. Reviewers requested use of
additional information if possible and, if not possible, inclusion of a
more thorough justification for relying on the old and widely varying
data in our global population estimate.
Response: The Act directs that we use the best scientific and
commercial data available in making our determinations. This rulemaking
was initially prompted by a petition to delist the species (see the
``Previous Federal Actions'' section of our proposed rule (February 20,
2008; 73 FR 9408)). In order to fulfill our requirements to respond to
the petition and complete the rulemaking process once begun, we are
statutorily required to make a determination at this time based on the
best scientific and commercial data currently available to us. We
recognize that additional research and coordinated efforts would yield
a more reliable and accurate global population estimate. We have used
the best available scientific and commercial data in developing our
global population estimate. However, we have not relied solely upon
this estimate in making our determination that the brown pelican no
longer warrants listing. This number is developed and presented in
efforts to provide the reader a general estimate of the scale of the
global population, allow comparisons with other available estimates,
and provide a summary and conclusion of the various estimates provided.
While the accuracy of the specific number cannot be determined due to
differences in survey methodology and information quality, the relative
scale of the number, in the hundreds of thousands, is useful in
demonstrating the degree of recovery the species has acheived and the
absence of significant threats to the species. We have expanded the
discussion under the ``Summary--Global Population Estimate'' section to
further explain our rationale in developing this estimate.
(3) Comment: The discussion of the significance of the Puerto Rico
brown
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pelicans makes it seem that the Service is saying these birds are not
important.
Response: In evaluating the brown pelican and whether it continues
to require regulatory protection under the Act, we have looked at the
species from a range-wide perspective first. The species' population
numbers have rebounded and threats have been removed or reduced to the
point that protection under the Act is no longer needed range wide.
Next, we assessed whether any population may be experiencing localized
threats over a significant portion of the range of the pelican such
that its loss would lead to the species as a whole being at a greater
risk of extinction. As discussed in ``Significant Portion of the
Range'' section below, we have determined that the Puerto Rico
population does not warrant listing as a significant portion of the
range of the species, although this analysis does not imply that any
subspecies, population, or subpopulation of brown pelican is not
important to the long-term conservation of the brown pelican. In
addition, once the pelican is delisted, brown pelicans will remain
protected by the Migratory Bird Treaty Act and numerous other
mechanisms, as discussed below. We will continue working with the
Puerto Rico Department of Natural Resources through the post-delisting
monitoring process to monitor the status of the brown pelican in Puerto
Rico.
(4) Comment: A complete study of the genetics of the entire species
would seem to be strongly warranted in order to further elucidate
unique, small breeding populations.
Response: We agree and encourage continued research on the brown
pelican; however, we don't believe a full understanding of the genetics
of each individual breeding population is required in order to make our
delisting decision, especially in the face of decreased threats and
increased conservation and management opportunities.
(5) Comment: While population numbers confirm that delisting is the
correct action, threats to the brown pelican still remain. There needs
to be monitoring of the brown pelican and the marine environment post-
delisting.
Response: Under section 4(g)(1) of the Act, we are required to
monitor all species that have been recovered and delisted for at least
5 years post-delisting. On September 30, 2009 (74 FR 50236), we
announced the availability of a draft post-delisting monitoring plan
for the brown pelican which we expect to finalize within a year. We do
not anticipate any of the factors currently affecting the brown pelican
to become a threat to the status of the species in the future; however,
if at any time during the monitoring program, data indicate that the
protective status under the Act should be reinstated, we can initiate
listing procedures, including, if appropriate, emergency listing.
(6) Comment: A peer reviewer noted that the productivity criterion
developed in the California Brown Pelican Recovery Plan was somewhat
subjective and based on comparisons to brown pelican productivity
elsewhere. Despite this problem, the peer reviewer notes that the
overall conclusions reached in the proposed rule concerning these
productivity criteria--that a significant recovery has occurred in the
Southern California Bight--are reasonable and logical.
Response: While recovery planning and the recovery criteria often
included in recovery plans provide useful tangible benchmarks for the
planning of conservation, the Act requires us to base listing and
delisting assessments on the status of the species and an