Endangered and Threatened Wildlife and Plants; 12-Month Petition Finding and Proposed Rule To Remove the Brown Pelican (Pelecanus occidentalis) From the Federal List of Endangered and Threatened Wildlife, 9408-9433 [E8-2829]
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9408
Federal Register / Vol. 73, No. 34 / Wednesday, February 20, 2008 / Proposed Rules
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; 12-Month Petition Finding
and Proposed Rule To Remove the
Brown Pelican (Pelecanus
occidentalis) From the Federal List of
Endangered and Threatened Wildlife
Fish and Wildlife Service,
Interior.
ACTION: Proposed rule and notice of
petition finding.
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AGENCY:
SUMMARY: Under the authority of the
Endangered Species Act of 1973, as
amended (Act), we, the U.S. Fish and
Wildlife Service (Service), propose to
remove the brown pelican (Pelecanus
occidentalis) from the Federal List of
Endangered and Threatened Wildlife
(List) due to recovery. This action is
based on a review of the best available
scientific and commercial data, which
indicates that the species is no longer in
danger of extinction, or likely to become
so within the foreseeable future. If this
proposal is finalized, the brown pelican
will remain protected under the
provisions of the Migratory Bird Treaty
Act. This document also constitutes our
12-month finding on a petition to delist
the brown pelican subspecies that
occurs along the Pacific Coast of
California and Mexico, including the
Gulf of California, and a petition to
delist the Louisiana population of the
brown pelican.
DATES: We will accept comments
received or postmarked on or before
April 21, 2008. We must receive
requests for public hearings, in writing,
at the address shown in the ADDRESSES
section by April 7, 2008.
ADDRESSES: You may submit written
comments and materials to us by any
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• U.S. mail or hand-delivery: Public
Comments Processing, Attn: RIN 1018–
AV28; Division of Policy and Directives
Management; U.S. Fish and Wildlife
Service; 4401 N. Fairfax Drive, Suite
222; Arlington, VA 22203.
We will not accept e-mail or faxes. We
will post all comments on https://
www.regulations.gov. This generally
means that we will post any personal
information you provide us (see the
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Public Comments section below for
more information).
FOR FURTHER INFORMATION CONTACT:
Adam Zerrenner, Field Supervisor, U.S.
Fish and Wildlife Service, Austin
Ecological Services Office, 10711 Burnet
Road, Suite 200, Austin, TX 78758;
telephone 512/490–0057, extension 248;
fascimilie 512/490–0974.
SUPPLEMENTARY INFORMATION:
Public Comments Solicited
We intend for any final action
resulting from this proposal to be as
accurate as possible. Therefore, we
solicit data, comments, or suggestions
from the public, other concerned
government agencies, the scientific
community, industry, Tribes, or any
other interested party concerning this
proposed rule. We particularly seek
comments and information concerning:
(1) Information about any threat (or lack
thereof) to the brown pelican; (2)
additional information concerning the
range, distribution, location of any
additional populations, and population
size of this species; (3) information on
habitat destruction and/or preservation
in relation to brown pelicans; (4)
impacts to the species from commercial
fisheries outside of the U.S.; (5) current
or planned activities in the species’
habitat and the possible impacts to this
species; (6) data on population trends;
(7) data on the status of brown pelicans
in the West Indies; (8) data suggesting
that any of the subspecies of brown
pelican require protection; and (9)
information pertaining to the
requirement for post delisting
monitoring. In addition, because we
have received information indicating
that one of the subspecies of brown
pelican discussed in this proposal,
Pelecanus occidentalis thagus, may be
considered a full species, we request
any additional information regarding
brown pelican taxonomy. Please note
that as we make our determination, we
will note but not consider comments
merely stating support or opposition to
the actions under our consideration
without providing supporting
information because section 4(b)(1)(A)
of the Act (16 U.S.C. 1531 et seq.)
directs that we make determinations as
to whether any species is a threatened
or endangered species ‘‘solely on the
basis of the best scientific and
commercial data available.’’
You may submit your comments and
materials concerning this proposed rule
by one of the methods listed in the
ADDRESSES section. Comments must be
submitted to https://www.regulations.gov
before midnight (Eastern Standard
Time) on the date specified in the DATES
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section. We will not accept comments
sent by e-mail or fax or to an address not
listed in the ADDRESSES section. We will
not accept anonymous comments; your
comment must include your first and
last name, city, State, country, and
postal (zip) code. Finally, we will not
consider hand-delivered comments that
we do not receive, or mailed comments
that are not postmarked, by the date
specified in the DATES section.
We will post your entire comment—
including your personal identifying
information—on https://
www.regulations.gov. If you provide
personal identifying information in
addition to the required items specified
in the previous paragraph, such as your
street address, phone number, or e-mail
address, you may request at the top of
your document that we withhold this
information from public review.
However, we cannot guarantee that we
will be able to do so.
Comments and materials we receive,
as well as supporting documentation we
used in preparing this proposed rule,
will be available for public inspection
on https://www.regulations.gov, or by
appointment, during normal business
hours, at the U.S. Fish and Wildlife
Service, Austin Ecological Services
Office (see FOR FURTHER INFORMATION
CONTACT).
The Act provides for a public hearing
on this proposed delisting, if requested.
Requests must be received within 45
days of the date of publication of this
proposal. Such requests must be made
in writing and addressed to Adam
Zerrenner, Field Supervisor, U.S. Fish
and Wildlife Service, Austin Ecological
Services Office (see FOR FURTHER
INFORMATION CONTACT).
Background
Currently listed brown pelican
populations 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; along the
Pacific Coast from British Columbia,
Canada, south through Mexico into
Central and South America; and in the
West Indies, but are occasionally
sighted throughout the U.S. (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 still occurs
throughout its historical range (Shields
2002, pp. 4–5). This proposed rule
includes relevant biological and life
history information for the brown
pelican. However, additional
information about the brown pelican’s
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biology and life history can be found in
the Birds of North America, No. 609
(Shields 2002, pp. 1–36).
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. Taxonomy of the brown
pelican subspecies has not been
critically reviewed for many years, and
the classification followed by the
American Ornithological Union (AOU
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. This proposed
delisting rule applies to the entire listed
species, which includes all brown
pelican (Pelecanus occidentalis)
subspecies.
For a review of the brown pelican’s
status, see the ‘‘Population Estimates’’
section below. For a review of the
threats in relation to the species status,
see the ‘‘Summary of Factors Affecting
the Species’’ section below.
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Previous Federal Action
Due to population declines of brown
pelicans, in 1970, we listed the species
as endangered under the Endangered
Species Conservation Act of 1969 (Pub.
L. 91–135, 83 Stat. 275). Brown pelicans
were included in the List of Threatened
and Endangered Foreign Species on
June 2, 1970 (35 FR 8495), and included
in the United States list of endangered
and threatened species on October 13,
1970 (35 FR 16047). The species was
subsequently listed under the
Endangered Species Act (Act) of 1973,
as amended (16 U.S.C. 1531 et seq.).
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On February 4, 1985, the Service
delisted the brown pelican in Alabama,
Florida, Georgia, South Carolina, North
Carolina, and points northward along
the Atlantic Coast (50 FR 4938).
However, the brown pelican continued
to be listed as endangered throughout
the remainder of its range, including
Mississippi, Louisiana, Texas,
California, Mexico, Central and South
America, and the West Indies.
On July 5, 1994, we received a
petition dated February 21, 1994, from
Joe L. Herring, Secretary, Department of
Wildlife and Fisheries, State of
Louisiana, requesting the Service
remove the brown pelican from the List
in Louisiana. The petition contained
information on successful pelican
reintroductions, colony expansions,
population numbers, and productivity
in Louisiana. We were not able to act on
the request, since the processing of
delisting actions was assigned the
lowest priority in the allocation of
available funding appropriations, as
described in the Federal Register (61 FR
64475; December 5, 1996). In 1999,
delisting actions were moved from the
Service’s listing program to the recovery
program, allowing us to address
requests and petitions to downlist and
delist species. This proposed rule
constitutes our 90-day and 12-month
findings for the Louisiana petition to
delist the brown pelican.
On December 14, 2005, we received a
petition from Craig Harrison, of the law
firm Hutton and Williams, representing
the Endangered Species Recovery
Council, to remove the California brown
pelican, the subspecies of brown pelican
occurring along the Pacific Coast of
California and Mexico, including the
Gulf of California, from the List. We
note that the taxon on the List is
Pelecanus occidentalis, and the petition
is specifically for the delisting of the
California brown pelican subspecies,
Pelecanus occidentalis californicus. The
petition contained information on
population size, trends, reproduction,
and distribution of the California brown
pelican, including information on the
status and management of the species in
Mexico. It contained information on the
elimination (e.g., banning of DDT) or
management of threats that originally
resulted in the brown pelican being
listed as endangered. On May 24, 2006
(71 FR 29908), we published a notice
announcing our 90-day finding for the
petition, in which we concluded that
the petition presented substantial
scientific or commercial information
indicating that the petitioned action
may be warranted. We then initiated a
12-month status review of the California
brown pelican to determine if delisting
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under the Act is warranted. This
proposed rule constitutes our 12-month
finding for the petition to delist the
California brown pelican.
On May 24, 2006, we also published
a notice announcing initiation of a
5-year review on the rangewide status of
the brown pelican (71 FR 29908). Under
the Act, we are required to review listed
species at least once every 5 years and
determine whether or not any species
should be removed from the List, or
reclassified from endangered to
threatened or from threatened to
endangered. The conclusion of this
review, which was based on the best
available scientific information,
indicates the currently listed brown
pelican population does not meet the
definition of an endangered or
threatened species under the Act
(Service 2007a, p. 46).
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, and because 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 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 non-breeding birds as
well. However, the information does
indicate the broad distribution of the
species and reflects the large global
population estimate of over 620,000
birds, which does not include birds
along the Atlantic coast of the U.S.,
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Florida or Alabama (Service 2007a, pp.
44–45).
Gulf of Mexico Coast
Mississippi—Brown pelicans are
currently not known to breed in
Mississippi, but the Great Backyard Bird
Count (GBBC) has documented brown
pelicans annually in Mississippi since
1999 (GBBC 2007, pp. 1–9). In 2003 and
2004, 244 and 261 pelicans,
respectively, were counted. There was
an increase to 403 pelicans in 2005, but
a large decrease to 54 in 2006 (GBBC
2007, pp. 5–8), which coincides with
Hurricane Katrina. However, in 2007,
334 brown pelicans were documented
(GBBC 2007, p. 9).
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, p. 1, 4).
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.
Numbers of successful nests are not
directly comparable to numbers of
individuals in historic estimates
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because they do not account for
immature or non-breeding 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) 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, p. 2–3). The highest count was in
2005 with 4,097 breeding pairs in 12
colonies (Service 2006, p. 2). This
number equates to 8,194 breeding birds,
which is substantially greater than
historical population estimates for
Texas. Numbers declined slightly in
2006 to 3,801 breeding pairs in six
nesting colonies (7,602 breeding birds)
(Service 2006, p. 2), possibly due to
hurricanes in 2005 (see discussion of
storm effects under Factor A), but they
remained above historical estimates.
The 2006 census numbers may be low
because survey data appear to be
missing for Sundown Island, which
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traditionally supports a large brown
pelican breeding colony. There were
1,676 breeding pairs nesting at
Sundown Island in 2007 (Erfling 2007a,
p. 1; https://www.sundownisland.org/
default.htm), which is comparable to
the number breeding there in 2005
(Service 2006, p. 2).
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 along this same
stretch of coast conducted in March
1986 counted 2,270 birds, down from
4,250 birds estimated in counts
conducted between December 1979 and
January 1980 (Blankinship 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. No 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.
West Indies
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. Raffaele
et al. (1998, pp. 224–225) describe the
brown pelican as ‘‘A common yearround 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.
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Migrants that breed in North America
augment local numbers primarily from
November to February.’’
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 historic record of
nesting.
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
found no breeding pelicans at one site
in 2002. 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 (IBAs) 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. See ‘‘Human disturbance of
nesting pelicans’’ under Factor A below
for discussions of possible reasons for
decline.
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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¨
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 16–36 pairs
during monitoring in 2001 and 2002
´
(Acosta-Cruz and Mugica-Valdes 2006,
p. 33). No estimates were given for other
nesting sites. Acosta-Cruz and Mugica´
Valdes (2006, p. 65) estimate the
population of brown pelicans in Cuba
falls within the range on 1,000 to 4,999
birds and that the population trend is
stable.
Summary of West Indies—Although
we do not have detailed information on
brown pelicans throughout the islands
of the West Indies, the distribution of
current breeding colonies reported by
Collazo et al. (2000, p. 42) is similar to
that reported by van Halewyn and
Norton (1984, pp. 174–175, 201).
Estimates of number of breeding pairs
differ between the two reports but the
studies differed somewhat in the sites
reported and neither provided detailed
methods for their estimates. Neither
Collazo et al. (2000, p. 63) nor van
Halewyn and Norton (1984, pp.174–175,
201) provided estimates for birds
nesting in Cuba, but Acosta-Cruz and
´
Mugica-Valdes (2006, p. 65) estimate the
population in Cuba falls within the
range on 1,000 to 4,999 birds.
Caribbean and Atlantic Coast of Mexico,
Central 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 6200 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
(Blankinship 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
(Blankinship 1987, p. 2).
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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
(pp. 144–149) variously report brown
pelicans as: ‘‘Common: high density,
likely to be seen many places,’’
‘‘Transient, present briefly as migrant,’’
‘‘Resident, species present all year,’’
‘‘apparently secure in Belize.’’ Brown
pelicans are also reported in one
reference as nesting on several cays, 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
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 in Panama, 582 brown
pelicans were counted (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
Humedales costeros de La Guajira
(coastal wetlands of La Guajira).
However, no estimate of numbers of
breeding birds was given.
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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 1700 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 non-breeding 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.
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
71,200 nesting pairs, which equates to
142,400 breeding birds (Henny and
Anderson 2007, p. 9). 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 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). The populations on Todos Santos
´
and San Martın islands were previously
extirpated in 1923 and 1974,
respectively; however, these were
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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 3,650 breeding
pairs, the Gulf of California population
is estimated at 42,970 breeding pairs,
and the mainland Mexico population
has about 12,880 breeding pairs
(Anderson 2007b; Henny and Anderson
2007, p. 9). 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 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, p. 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 non-breeding 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 non-breeding 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
number of brown pelicans within
Nicaragua falls within the range 1,001–
5,000, but do not indicate locations or
breeding status.
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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 1,976 nest
numbers from Coiba Island (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.
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
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birds. Santander et al. (2006, p. 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
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
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.
Summary—Global Population
Estimates
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. 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.
However, because these estimates are
the best available information, we
attempted to use some conservative
assumptions in tabulating these data in
order to make a conservative estimate of
the global population size of the brown
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pelican (Service 2007a, pp. 43–45 and
60–62). This total, or global estimate, is
for the listed brown pelican, which does
not include the Atlantic coast of the
U.S., 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
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 U.S.,
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 non-breeders 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).
Recovery plans are not regulatory
documents and are instead intended to
provide guidance to the Service, States,
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9413
and other partners on methods of
minimizing threats to listed species and
on criteria that may be used to
determine when recovery is achieved.
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. In that instance, the
Service may judge that, overall, the
threats have been minimized
sufficiently and the species is robust
enough to justify reclassifying the
species from endangered to threatened
or perhaps delisting 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. Analyzing the degree of
recovery of a species is also an adaptive
management process that may or may
not fully follow the guidance provided
in a recovery plan. 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
delisted populations and the currently
listed Texas, Louisiana, and Mississippi
populations, 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). The recovery plan
states a general objective to re-establish
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. As of 2005
(prior to Hurricanes Katrina and Rita),
11 sites in Louisiana were being used
for nesting by brown pelicans: Brush
Island, Martin Island, North Island,
Pelican Point, West Breton Island,
Baptiste Collette, Queen Bess Island,
Wine Island, Raccoon Island, Rabbit
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Island, and Shallow Bayou. This list
includes 7 previously unknown sites
(Hess and Linscombe 2006, pp. 1–4,
7–8). In 2006, nesting occurred at 15
sites that included the previously
mentioned 11. Hurricane-caused habitat
degradation forced many birds to seek
out new nesting locations including
three additional sites in the Pelican
Point area, and one on East Queen Bess
Island (Hess and Linscombe 2007, pp. 1,
3). As of 2006, 12 sites in Texas were
being used for nesting by brown
pelicans: Marker 52 Spoil Island, North
Deer Island, Evia Island, Sunfish Island,
Shamrock Island, Deadman Islands,
South Pass Islands A and B, Pelican
Island, Sundown Island, Little Pelican
Island, and Dressing Point (Service
2006, p. 2). 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 support 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
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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 (2,289 compared to 593
individuals). 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
appropriate for determining whether the
brown pelican is recovered globally.
The second recovery criterion is the
more important of the two 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 5year observed mean, the estimated
number is consistent with the recovery
criterion for number of 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
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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, p. 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 species’ 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 for the
subspecies to be considered for
delisting: (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 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. 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, the
productivity criterion for delisting,
while it has improved greatly since the
time of listing and has neared the
criterion for delisting a few times, 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
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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
reached, reproduction has been
sufficient to maintain a stable
population for over 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 and that current
productivity is sufficient to maintain a
viable population of brown pelicans.
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 all together. No
subsequent revisions have been made to
any of these original recovery plans. No
single recovery plan covers the entire
range of the species, and the remainder
of the range outside the U.S., including
Central America, South America, and
most of the West Indies is not covered
by a recovery plan. Thus, these focus
areas for recovery, which do not have
formal or regulatory distinction, are
outdated. 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
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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 proposal is based largely
on the analysis of threats in our recently
completed 5-year review (Service 2007a,
pp. 1–66). This review is available at
https://ecos.fws.gov/docs/
five_year_review/doc1039.pdf.
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
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. 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
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any portions of brown pelican’s range in
danger of extinction or likely to become
endangered within the foreseeable
future.
As discussed below in our analysis of
factors affecting the species, we do not
foresee any changes in the current
protections for brown pelican. For
example, we do not expect any
significant changes to current nonEndangered Species Act habitat
protections, regulations affecting
pesticide use and licensing, the
Migratory Bird Treaty Act, MagnusonStevens Fishery Conservation and
Management Act, or the global
Stockholm Convention on Persistent
Organic Pollutants. We could consider
that many of these protections would
remain in place in perpetuity. However,
considering this as a timeframe for
analysis could introduce a considerable
level of uncertainty and it may not be
reasonable to assume that we can
project an analysis out in perpetuity.
Therefore, for the purposes of our
analysis, we considered as a lower
bound the timeframe over which it
would be reasonable to expect
population level or demographic effects
of threats to be detected and to put the
species at risk of becoming endangered.
Factors most likely to affect population
levels and key demographic
characteristics of brown pelicans
include those that affect reproduction
over a period of several years, and
include factors such as disturbance of
nest sites, contaminants, and
availability of prey. Therefore, for the
purposes of this proposed rule, we
consider ‘‘foreseeable future’’ for the
brown pelican at a minimum to be 30
years, since it is a reasonable timeframe
for analysis of factors identified that
could affect the species in the future
and as they relate to brown pelican
biology. While average life spans are not
known, fewer than 2 percent are thought
to live past 10 years of age, and the
oldest known individual was 43 years
old (Schreiber and Mock 1988, p. 178).
Additionally, since age at first nesting is
generally 3 to 5 years (Shields 2002, p.
18), the average brown pelican breeds at
4 years of age, thereby replacing itself
within 8 years. Therefore, 30 years,
which incorporates one long life cycle
and 10 possible generations, represents
a reasonable biological timeframe to
determine if threats could be significant.
The following analysis examines all
five factors currently affecting, or that
are likely to affect, the brown pelican
distribution that is currently listed
within the foreseeable future.
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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, predator-free coastal islands.
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 off-shore 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., Launcularia 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
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 and protection 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
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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, p. 1097–1099; Anderson
2007a), 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 may
utilize other nesting substrates, and they
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 only affect brown pelicans
on a local scale 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
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 habitat destruction
currently threatens brown pelicans, nor
do we believe it will it 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
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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, and
while a figure for loss of barrier islands
would be a more appropriate measure of
impacts to brown pelicans, we are not
aware of any estimates for barrier island
loss. 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
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
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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, 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, there are numerous 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), 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
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Wetlands Conservation and Restoration
Task Force 2006, p. 13).
Three other plans that may be
implemented are Coast 2050 and the
Louisiana Coastal Area Ecosystem
Restoration (LCA) Plan, both related to
the CWPPRA, and the Draft Coastal
Impact Assistance Plan. Although not
yet implemented, Coast 2050 and the
LCA plan also focus on the protection
and restoration of Louisiana coastal
areas, including barrier island
protection and restoration. While these
plans are not considered as existing
regulatory mechanisms for the purposes
of this proposed delisting and are not
designed specifically to benefit brown
pelicans, we are aware that they may
provide opportunities for us to monitor
and to continue to reduce and minimize
the threats to brown pelicans from
habitat loss and degradation caused by
storms in the Louisiana Gulf Coast
region after they are delisted, and
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
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 (Avicennia germinans),
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 non-woody 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
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hurricanes, storms, and erosion have
been documented (Wilkinson et al.
1994, p. 425; Hess and Linscombe 2006,
p. 4), we believe brown pelicans are
capable of recovering from these 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 time frame, 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 fifteen 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
to expect State and Federal agencies to
continue active maintenance and
restoration of barrier islands through
programs such as the CWPPRA. 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.
Human disturbance of nesting
pelicans. Adverse effects on nesting
pelicans from human disturbance by
recreationists, scientists, educational
groups, and fishermen have been well
documented (Anderson 1988, p. 342;
Anderson and Keith 1980, pp. 68–69).
Disturbance at nesting colonies, such as
walking among or near nests, has been
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shown to adversely affect reproductive
success of pelicans, and even result in
abandonment of nests or entire colonies
(Anderson and Keith 1980, p. 69).
Collier et al. (2003, pp. 112–113) offer
human disturbance as the cause of a
suspension of breeding activity in a
brown pelican colony on St. Martin in
the Lesser Antilles. The colony was near
a resort with heavy boat and jet ski use.
When a jet ski passed within about 400
m (1,312 ft) of a colony 40 pelicans
flushed, leaving their nests unattended
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
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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.
Future conservation actions in Mexico
that are not a factor in our proposal to
delist the brown pelican, but 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 for nest sites and to prevent
human disturbances to U.S. nesting
colonies, as well as the protections
afforded by State laws, 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 below 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
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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
result in population declines of brown
pelicans throughout all of the species’
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 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 to not only
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 if 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). Audubon staff assess the conditions
of brown pelican islands throughout the
year in Texas (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, both in Corpus 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
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cooperation with the Corps, Texas Parks
and Wildlife Department, and the
Service, 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 2007b). Signs
advising the public to avoid landing
were posted at each island listed above;
the sign at Alligator Point was lost due
to erosion, but there are plans to replace
the sign this year (Erfling 2007b).
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 who 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
probably only subject to occasional
offshore recreational and commercial
fishing activity.
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 (IBAs) (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
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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 (small, low
islands) (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
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 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)
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9419
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, the California
Department of Fish and Game (CDFG)
designated the waters adjacent to
nesting brown pelican habitat on West
Anacapa 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
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).
Caribbean Coast of Mexico, and
Central and South America. 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.
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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, p. 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
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, all seven
sites where brown pelican were
documented to occur by Moreno and
Buelvas (2005, p. 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
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16:49 Feb 19, 2008
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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—Proabons, an agency in Peru’s
Ministry of Agriculture, protects and
manages brown pelican nesting islands,
which are collectively referred to as
guano 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
Peruvian government. 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).
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 regarding nesting habitat,
conservation efforts are continuing to
positively affect 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
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scale. Threats from human disturbance
of nesting colonies throughout most of
the species’ range have been abated
through protection efforts, including
designation of National Parks and
Biosphere Reserves, signage to deter
people from entering colonies, and
restricted access. While 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 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).
Roost 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
(Jaques and Anderson 1987, pp. 14, 19;
Briggs et al. 1981, pp. 7–8). In other
areas, brown pelicans generally also 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).
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
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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
(CCNM), 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 CCNM.
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
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). For the next 5 years, a
maximum of 25 missile launches per
year at Vandenberg AFB are estimated
(Frye 2006). Therefore, potential
impacts from missile launches are
minimal because they are temporary in
nature and will likely only occur a few
times per month.
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The Sonny Bono Salton Sea National
Wildlife Refuge, inland from San Diego,
is also used for roosting during the postbreeding season, supporting and
protecting 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
the central and southern California coast
is in preparation that will allow
conservation agencies to evaluate the
overall status of roosting habitat and
help prioritize roost sites for protection
(Gorbics et al. 2004, p. 1). In addition,
the following projects will benefit
brown pelicans, regardless of the brown
pelican listing status: American Trader
Restoration Plan (ATTC), Command Oil
Spill Restoration Plan, Torch/Platform
Irene Restoration Plan, 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, and one component
of all these plans is to reduce human
disturbance at roost sites in central and
southern California through education,
monitoring, and enforcement (ATTC
2001, p. 16; Command Oil Spill Trustee
Council 2004, p. 60; Torch/Platform
Irene Trustee Council 2006, p. 33; MSRP
2005, p. D6–1). ATTC also began 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
pelicans have not used the platform yet,
ATTC is exploring other sites to
enhance or create new roosts in
southern California (ATTC 2006, p. 1).
If the platform is successful, the MSRP
may duplicate this effort in additional
locations.
While some roosting habitat in the
United Sates 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. Nevertheless, the
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9421
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 endanger 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.),
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 offshore area within 30
to 50 km (18 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 U.S. 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 (AFMP). Amendment
8 to the AFMP, adopted December 15,
1999 (64 FR 240), changed the name of
the AFMP to the CPSFMP and added
Pacific sardine (Sardinops sagax),
Pacific mackerel (Scomber japonicus),
jack mackerel (Trachurus symmetricus),
and market squid (Loligo opalscens) to
the fishery management unit (CPSFMP
1998, p. 1–1). Amendment 8 divided
these species into actively managed and
monitored categories. 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
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(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 current
harvest is 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
AFMP 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 CPFSMP 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).
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 U.S.
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 in recent years, 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
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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 nor the Caribbean Fishery
Management Council (Web sites
accessed: https://www.gulfcouncil.org/,
and https://www.caribbeanfmc.com/), in
the U.S., 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 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,
interannual (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).
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McNease et al. (1994, p. 10) found
that severe freezes in Louisiana 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
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.
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 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 (100 Stat. 3585),
which authorizes the purchase of
wetlands from Land & Water
Conservation Fund monies; North
American Wetlands Conservation Act of
1989 (103 Stat. 1968) which provides
funding for wetland conservation
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programs in Canada, Mexico, and the
United States; Anadromous Fish
Conservation Act of 1965 (79 Stat.
1125), 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 (96 Stat. 1653), as
amended by the Coastal Barrier
Improvement Act of 1990, which
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. 1451–1464),
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 of coastal wetlands and
fishery resources; Shore Protection Act
of 1988; Outer Continental Shelf Lands
Act of 1954, as amended in 1978 and
1985; National Ocean Pollution
Planning Act of 1978; Oil Pollution Act
of 1990; Act to Prevent Pollution From
Ships of 1980; Marine Pollution and
Research and Control Act of 1989;
Ocean Dumping Ban Act of 1988; and
Marine Protection, Research, and
Sanctuaries Act of 1988. These laws and
regulations, taken collectively, help
ensure the conservation of brown
pelicans and their habitat.
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. Threats from
human disturbance of nesting colonies
throughout most of the species’ range
have been abated through protection
efforts, including designation of
National Parks and Biosphere Reserves,
signage to deter people from entering
colonies, and restricted access. While
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
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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
U.S. and elsewhere is limiting brown
pelican populations by reducing the
˜
species’ fish prey base. El Ninos and
severe freezes may impact brown
pelicans on a short-term, localized basis,
but these events do not threaten the
continued existence of 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 brown pelican is not
threatened or endangered throughout all
of its range within the foreseeable future
by the present or threatened destruction,
modification, or curtailment of its
habitat or range.
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
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) of 1918 (16 U.S.C. 703–711; 40
Stat. 755). 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). We do not
have any information to indicate that
overutilization for commercial,
recreational, scientific, or educational
uses is occurring within areas covered
by the MBTA or elsewhere throughout
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the species’ range. Therefore, we do not
believe overutilization will endanger the
brown pelican throughout all of its
range in the foreseeable future.
C. Disease or predation
Several diseases have been identified
as causing illness and mortality of
brown pelicans. The diatom (an algae)
Pseudo-nitzchia australis 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
because occurrences are few and selflimiting, we do not believe impacts from
disease 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 as causing the mortality of
white pelicans. 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).
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
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been reported in brown pelicans (50 FR
4942), 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.
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).
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
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
disturbances, egg and nest predation by
mammals and other birds does not
appear to impose a significant limitation
on brown pelican reproduction.
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
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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
threaten the species throughout all of its
range 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. Another Federal law not
cited under the other factors that will
continue to offer some form of
protection for the brown pelican is the
Lacey Act which helps the United States
and other foreign countries enforce their
wildlife conservation laws, including
the protections afforded brown pelicans
under MBTA. In addition to these laws
that provide direct protection to the
brown pelicans, the Clean Water Act
and the Federal Insecticide, Fungicide,
and Rodenticide Act of 1996 (FIFRA; 7
U.S.C. 136 et seq.) provide regulations
indirectly through contamination
prevention, which contributes to habitat
protections. 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.
E. Other Natural or Manmade Factors
Affecting Its Continued Existence
Natural Factors
This discussion addresses direct
mortality of brown pelicans. See Factor
A for impacts to habitat from natural
weather events such as storms and El
˜
Nino. Boersma (1978, p. 1482) reported
˜
El Nino-season starvation of nestling
brown pelicans in the Galapagos
Islands. The 1982–83, 1986–87, and
˜
1991–1994 El Nino events may have
reduced the number of nesting brown
pelicans in those years at Cayo Conejo,
Puerto Rico (Schreiber 1999, p. 12). In
extreme cases adult mortality has
˜
resulted from El Nino events (Shields
2002, p. 32), for example, during the
˜
especially severe El Nino (Southern
Oscillation) of 1983 (Duffy 1986, p.
591). Mortality was not noted during the
less-severe event of 1978 (Boersma
1978, p. 1482). Shields (2002, p. 23, and
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reference cited within) states that food
˜
shortages as a result of El Nino and
other climatic and oceanographic events
may result in abandonment of nests and
starvation of nestlings, but rarely results
in adult mortality except in extreme
events. Because brown pelicans are long
lived, such short-term breeding failures
have little impact on long-term
population viability.
Storms accompanied by severe tidal
flooding can have a significant negative
effect on brown pelican productivity
(McNease et al. 1994, p. 10). While some
adults may be killed during storm
events, most impacts result in juvenile
mortality and reduced fledgling
production (Wilkinson et al. 1994, p.
425; Hess and Linscombe 2006, p. 4).
Additionally, eggs and nestlings may be
lost due to flooding (Hess and
Linscombe 2006, p. 23) and nests built
in trees are easily dislodged and
destroyed during strong winds or major
storms (Jiminez 2004, pp. 12–17; Saliva
1989). While McNease et al.’s (1994, p.
10) observations indicated a female that
has produced eggs or nestlings will not
nest again in the same season, Hess and
Linscombe (2006, pp. 3, 7, 23) found
pelicans rebuilding new nests on top of
flooded and damaged nests.
In addition to freezes in Louisiana
limiting brown pelican foraging and
resulting in fish mortality, as discussed
above under Factor A, McNease et al.
(1994, p. 10) found effects from severe
freezes included high initial brown
pelican mortality from hypothermia,
prolonged exposure to low
temperatures, and death while plungediving into ice-covered water. However,
severe freeze events are infrequent
(McNease et al. 1994, p. 10) and have
not precluded the Louisiana population
from growing to large numbers since the
restocking program began in the 1960s.
These natural factors may adversely
affect brown pelicans on a short-term,
localized basis, but do not pose a
rangewide threat to the continued
existence of the species. These factors
generally affect only a small number of
individuals, affect only a localized area,
or affect reproductive success for a
single season. The pelican is a longlived species that has evolved with
natural phenomena such as variation in
food resources, winter storms, and
hurricanes. These factors are only
significant when population sizes are
small and reproduction is limited.
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
natural events will endanger the species
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throughout all of its range in the
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Manmade Factors
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).
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 thinshelled 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, and for
designating the species as endangered,
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 population-
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wide reproductive impairment in brown
pelicans (Gress 1995, p. 92).
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 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 U.S.
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://
www.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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www.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 U.S.
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).
Polychlorinated biphenyls (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 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
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organism that transmits disease, such as
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://www.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 U.S. 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.
An important regulatory mechanism
affecting brown pelicans is the
requirement that pesticides be registered
with the EPA. Under the authority of the
FIFRA, 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
‘‘registration,’’ which permits their
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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 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 occur only 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
contaminant-caused mortality and
widespread reproductive failures are
unlikely to occur in the future.
Therefore, we do not believe pesticides
and contaminants will endanger the
brown pelican throughout all of its
range within 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 threat that is likely to
endanger 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).
Superficially embedded hooks can often
be removed without damage; however, a
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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 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).
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
not likely to threaten or endanger the
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brown pelican throughout all of its
range 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
(ATTC 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 (ATTC 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 (ATTC 2001, p. 10).
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
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
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likelihood of spills because it reduces
the probability of vessel-to-vessel and
vessel-to platform collisions. However,
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 the Coronados Islands
in Mexico (Carter et al. 2000, p. 436).
However, because tanker spills are
localized, we do not believe this impact
will become a threat that will endanger
the brown pelican throughout all of its
range 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, and there is currently a
moratorium on new oil platforms in
State and Federal waters (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; however,
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.
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
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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 U.S. 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 part 254). Several Federal and
State laws were instituted in the 1970s
to 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,
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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 (CERCLA), as amended (42
U.S.C. 9601 et seq.), the Oil Pollution
Act of 1990 (OPA) (33 U.S.C. 2701 et
seq.), and the Federal Water Pollution
Control Act or Clean Water Act (CWA),
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
(Environmental Protection Agency
2007a, Environmental Protection
Agency 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 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,
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). Although 117 brown
pelicans were reported as affected by
the 2001 spill in the Galapagos Islands
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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 oil-producing 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.
1). Because brown pelicans are also
protected by the MBTA, these
modifications to prevent mortalities are
expected to remain in place.
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
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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. 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).
Conclusion
As required by the Act, we considered
the five potential threat factors 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 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.
The primary reason for severe
declines in the brown pelican
population in the United States, and for
designating the species as endangered,
was 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 U.S. has
shown a dramatic recovery, and
although annual 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 enough
from past exposure to warrant a
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proposal for 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, the 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
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
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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.
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/
Detail_ChemReg.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 no longer
requires the protection of the Act.
Therefore, we propose to remove the
brown pelican from the List of
Endangered and Threatened Wildlife.
Having determined that the brown
pelican does not meet the definition of
threatened or endangered, 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
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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. DOI 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
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.
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 unimportant 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
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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
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.
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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
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, which superficially suggest that
Puerto Rico warrants further
consideration. However, Puerto Rico
represents a very small portion of the
global population of brown pelicans,
both numerically and geographically.
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 have been identified. 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,
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. Brown pelicans in Puerto Rico
belong to the subspecies of brown
pelican distributed throughout the West
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Indies and along the Caribbean coasts of
Colombia and Venezuela. We currently
have no information to indicate that
birds in Puerto Rico are genetically
different from other members of the
Caribbean subspecies, or that genetic
exchange among other areas in the
Caribbean is limited, and therefore
cannot conclude that brown pelicans in
Puerto Rico contribute meaningfully to
resiliency, redundancy, or
representation of the species. 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. In
summary, in our analysis of the five
listing factors, we did not identify any
significant continuing threats in any
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 propose to remove it from
the Federal List of Endangered and
Threatened Wildlife.
Effect of This Rule
This rule, if made final, would revise
50 CFR 17.12(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.
If this species is removed from the
List of Endangered and Threatened
Wildlife, the prohibitions and
conservation measures provided by the
Act, particularly through sections 7 and
9, of the Act would no longer apply.
Removal of the brown pelican from the
List of Endangered and Threatened
Wildlife would relieve Federal agencies
from the need 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. It will not, however, affect
the protection given to all migratory
bird species under the MBTA. To
understand the implications of this
proposed rule, it is important to review
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the changes in protection for brown
pelicans that will occur should this
proposed rule become final.
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
(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.
Monitoring Techniques—We will
coordinate with other Federal agencies,
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9431
State resource agencies, interested
scientific organizations, and others as
appropriate to develop and implement
an effective monitoring program to track
the population status of the brown
pelican. The minimum parameter to be
used to evaluate population trends will
be surveys of nesting birds to assess the
number of nesting pairs and their
productivity in each of the colonies.
These types of surveys most efficiently
overlap ongoing surveys for other sea
birds and provide a quick overview of
the status of the species. We will also
cooperate with and encourage
continued monitoring of nesting
populations in other countries and
examine survey reports with
comparable data when available.
In addition to the nesting bird and
productivity surveys, we will review the
following information, when available,
that will help to evaluate the status of
the species in more detail.
(1) Contaminants—To determine if
some individual pelicans are still
experiencing reduced reproductive
success caused by the presence of
residual DDT contamination, eggshell
thickness and contaminant
concentrations in non-viable eggs will
be analyzed to determine the current
level of contaminant exposure. In
addition, information will be gathered
from work on other similar sea birds as
an indicator of potential problems.
(2) Prey Availability—To determine if
prey availability is impacting pelican
productivity in the future, we will
obtain and examine the annual Stock
Assessment and Fishery Evaluation
report written by the Pelagic Fisheries
Management Council (required by the
Coastal Pelagic Species Fisheries
Management Plan). This report details
any significant changes or trends in
pelagic fish populations, fisheries, or
marine ecosystems, documents harvest
levels, and assesses the success of state
and Federal fishery management
programs. Additionally, we will also
obtain and examine any reports
produced by either the Gulf Coast or
Caribbean Fishery Management
Councils.
(3) Dietary Composition—To
determine the predominant prey
species, we will collect and analyze diet
samples from brown pelicans. In
combination with information on prey
availability, this will help us to monitor
how reproductive success is responding
to prey availability.
(4) Habitat Protection—To monitor
the status of brown pelicans, we will
review conservation and management
actions taken on certain properties
including, but not limited to, those
owned by (1) the National Park Service;
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(2) the Fish and Wildlife Service,
including National Wildlife Refuges; (3)
the Department of Defense; (4)
international reserves or biospheres; and
(5) private lands.
(5) Disease—To monitor pelican
mortalities from diseases such as West
Nile virus, avian influenza, or avian
botulism, we will review information
gathered from work on other similar sea
birds.
There has never been a coordinated
rangewide monitoring plan for the
brown pelican and we do not believe a
monitoring effort of this magnitude is
necessary in order to meet our
requirements under 4(g)(1) of the Act.
Whenever possible, we will use the
results of on-going monitoring
conducted by States, Federal agencies,
and other partners. Following are
descriptions of ongoing brown pelican
and/or sea bird monitoring efforts that
we believe will continue in the future.
Taken together, we believe these
separate monitoring efforts will provide
an overview of the status of the species
as a whole.
(1) Texas Colonial Waterbird Count
(TCWC)—This program is organized by
the Service, Texas Parks and Wildlife
Department, Texas Audubon Society,
and academic institutions. TCWC has
tracked population trends in Texas for
the brown pelican since 1972.
(2) LDWF annual surveys—LDWF
conducts aerial surveys annually,
counting numbers of brown pelican
nests and fledglings. These surveys
generally begin in March and occur
monthly through July. Multiple surveys
allow for preliminary estimates of
reproductive success each year.
Additionally, LDWF periodically
conducts wading and seabird colony
surveys in Louisiana.
(3) Roost Atlas—This effort is
organized and funded by the Service,
California Department of Fish and
Game, American Trader Trustee
Council, and private contractors.
Expected to be finished by 2009, it will
collate existing brown pelican roost
survey data along the coast of California
into a roost atlas for use by managers to
identify and prioritize important roost
sites for conservation and restoration.
Completion of the roost atlas will assist
with identifying roost sites for
continued survey or monitoring efforts.
(4) The Great Backyard Bird Count
(GBBC)—This program is organized by
Cornell Lab of Ornithology and the
National Audubon Society. Four-day
surveys are conducted in February of
each year.
(5) National Health Institute—This
program is managed by the U.S.
Geological Survey. Its mission is to
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provide information, technical
assistance, research, education, and
leadership on national and international
wildlife health issues. As part of this
role, it collects data and tracks avian
diseases and mortality, including data
on brown pelicans.
Following are descriptions of ongoing
or future planned brown pelican and
other restoration projects we expect to
contribute information concerning the
status of threats to the species. We
expect implementation of these
programs and their associated
monitoring programs will provide such
information as the amount, protection,
and restoration of brown pelican
habitat, as well as the effectiveness of
efforts to reduce disturbance and
incidental mortality of brown pelicans.
(1) Coastal protection and restoration
funding in Louisiana—Because
Louisiana coastal land loss has broad
negative implications beyond solely the
effects to nesting brown pelicans (e.g., to
the state economy, oil and gas
production, navigation security,
fisheries and flyways, and strategic
petroleum reserve facilities), coastal
habitat protection and restoration has
been and will continue to be a priority
for Louisiana. Currently there are
several laws and programs aimed at
protecting and restoring coastal
wetlands (including barrier islands) in
Louisiana. They include: the Coastal
Wetlands Planning, Protection, and
Restoration Act (CWPPRA), Coast 2050,
the Louisiana Coastal Area Study (LCA),
the Energy Recovery Act of 2005, and
the Coastal Protection and Restoration
Authority of Louisiana’s Draft
Comprehensive Coastal Protection
Master Plan.
(2) The Corps’ Beneficial Use of
Dredged Material Program in
Louisiana—The New Orleans District of
the Corps beneficially uses
approximately 11.1 million yds3 (8.5
million m3) of dredged material each
year in the surrounding environment
(Corps 2004; p. xi) and these activities
are expected to continue.
(3) American Trader Restoration
Plan—This plan is implemented by the
ATTC, Service, CDFG, and National
Oceanic and Atmospheric
Administration (ATTC 2001).
(4) The Command Oil Spill
Restoration Plan—This plan is
implemented by the Command Oil Spill
Trustee Council, Service, CDFG,
California Department of Parks and
Recreation, California State Lands
Commission, and National Oceanic and
Atmospheric Administration (Command
Oil Spill Trustee Council 2004).
(5) The Luckenbach Restoration
Plan—This plan is implemented by the
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S.S. Jacob Luckenbach Oil Spill Trustee
Council, Service, CDFG, National Park
Service, and National Oceanic and
Atmospheric Administration
(Luckenbach Trustee Council 2006).
(6) The Montrose Settlements
Restoration Program—Implemented by
the Montrose Trustee Council, National
Oceanic and Atmospheric
Administration, U.S. Fish and Wildlife
Service, National Park Service,
California Department of Fish and
Game, California Department of Parks
and Recreation, and California State
Lands Commission (MSRP 2005).
(7) The Torch/Platform Irene
Restoration Plan—This plan is
implemented by the Torch/Platform
Irene Trustee Council, Service, CDFG,
U.S. Department of Air Force—
Vandenberg AFB, and California State
Lands Commission (Torch/Platform
Irene Trustee Council 2006).
At the end of the post-delisting
monitoring period, we will review all
available monitoring data to determine
whether relisting, continuation of
monitoring, or termination of
monitoring is appropriate. We will also
consult with the States of California,
Texas, and Louisiana and other partners
to determine the need for future
monitoring efforts.
We will take appropriate action if,
during or after the monitoring effort, if
new information suggests that the
brown pelican meets the definition of
threatened or endangered. We will
consider evidence of any factors
significantly affecting the status of the
species which may indicate that a
serious decline is occurring or is likely
to occur. These factors include, but are
not limited to the following: (a)
Contaminant-related concerns which
result in mortality or effects on breeding
activities; (b) declining numbers of
occupied nesting areas; (c) declining
reproduction; (d) significant changes in
distribution; and (e) downward trends
in overall population status not as a
result of temporary natural factors (e.g.,
˜
El Nino or storm events).
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. A Federal agency may not
conduct or sponsor and a person is not
required to respond to a collection of
information unless it displays a
currently valid OMB control number.
OMB approval is required if information
will be collected from 10 or more
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persons (5 CFR 1320.3). ‘‘Ten or more
persons’’ refers to the persons to whom
a collection of information is addressed
by the agency within any 12-month
period, and to any independent entities
to which the initial addressee may
reasonably be expected to transmit the
collection of information during that
period, including independent State,
territorial, Tribal, or local entities and
separately incorporated subsidiaries or
affiliates. For the purposes of this
definition, ‘‘persons’’ does not include
employees of the respondent acting
within the scope of their employment,
contractors engaged by a respondent for
the purpose of complying with the
collection of information, or current
employees of the Federal government
when acting within the scope of their
employment, but it does include former
Federal employees. The draft postdelisting monitoring plan that will be
developed for the brown pelican may
contain a requirement for information
collection; however, we do not
anticipate that it will affect 10 or more
persons, as defined above. Therefore,
OMB approval and a control number are
not needed for the data collection
contained in the monitoring plan. As
the monitoring plan is further
developed, if it becomes necessary to
collect this information from 10 or more
respondents per year, we will first
obtain approval from OMB.
National Environmental Policy Act
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We have determined that
Environmental Assessments or
Environmental Impact Statements, as
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16:49 Feb 19, 2008
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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
published a notice outlining our reasons
for this determination in the Federal
Register on October 25, 1983 (48 FR
49244).
Clarity of This Regulation
We are required by Executive Orders
12866 and 12988 and by the
Presidential Memorandum of June 1,
1998, to write all rules in plain
language. This means that each rule we
publish must:
a. Be logically organized;
b. Use the active voice to address
readers directly;
c. Use clear language rather than
jargon;
d. Be divided into short sections and
sentences; and
e. Use lists and tables wherever
possible.
If you feel that we have not met these
requirements, send us comments by one
of the methods listed in the ADDRESSES
section. To better help us revise the
rule, your comments should be as
specific as possible. For example, you
should tell us the numbers of the
sections or paragraphs that are unclearly
written, which sections or sentences are
too long, the sections where you feel
lists or tables would be useful, etc.
References Cited
A complete list of all references we
cited is available upon request from the
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9433
Austin Ecological Services Office (see
FOR FURTHER INFORMATION CONTACT).
Authors
The primary author of this proposed
rule is the Austin Ecological Services
Office (see FOR FURTHER INFORMATION
CONTACT).
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Proposed Regulation Promulgation
Accordingly, we propose to amend
part 17, subchapter B of chapter I, title
50 of the Code of Federal Regulations as
set forth below:
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
Authority: 16 U.S.C. 1361–1407; 16 U.S.C.
1531–1544; 16 U.S.C. 4201–4245; Pub. L. 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.
Dated: February 8, 2008.
Dirk Kempthorne,
Secretary of the Interior.
H. Dale Hall,
Director, Fish and Wildlife Service.
[FR Doc. E8–2829 Filed 2–19–08; 8:45 am]
BILLING CODE 4310–55–P
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Agencies
[Federal Register Volume 73, Number 34 (Wednesday, February 20, 2008)]
[Proposed Rules]
[Pages 9408-9433]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-2829]
[[Page 9407]]
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Part II
Department of the Interior
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Fish and Wildlife Service
50 CFR Part 17
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Endangered and Threatened Wildlife and Plants; 12-Month Petition
Finding and Proposed Rule To Remove the Brown Pelican (Pelecanus
occidentalis) From the Federal List of Endangered and Threatened
Wildlife; Proposed Rule
Federal Register / Vol. 73, No. 34 / Wednesday, February 20, 2008 /
Proposed Rules
[[Page 9408]]
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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; 12-Month Petition
Finding and Proposed Rule To Remove the Brown Pelican (Pelecanus
occidentalis) From the Federal List of Endangered and Threatened
Wildlife
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Proposed rule and notice of petition finding.
-----------------------------------------------------------------------
SUMMARY: Under the authority of the Endangered Species Act of 1973, as
amended (Act), we, the U.S. Fish and Wildlife Service (Service),
propose to remove the brown pelican (Pelecanus occidentalis) from the
Federal List of Endangered and Threatened Wildlife (List) due to
recovery. This action is based on a review of the best available
scientific and commercial data, which indicates that the species is no
longer in danger of extinction, or likely to become so within the
foreseeable future. If this proposal is finalized, the brown pelican
will remain protected under the provisions of the Migratory Bird Treaty
Act. This document also constitutes our 12-month finding on a petition
to delist the brown pelican subspecies that occurs along the Pacific
Coast of California and Mexico, including the Gulf of California, and a
petition to delist the Louisiana population of the brown pelican.
DATES: We will accept comments received or postmarked on or before
April 21, 2008. We must receive requests for public hearings, in
writing, at the address shown in the ADDRESSES section by April 7,
2008.
ADDRESSES: You may submit written comments and materials to us by any
one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
U.S. mail or hand-delivery: Public Comments Processing,
Attn: RIN 1018-AV28; Division of Policy and Directives Management; U.S.
Fish and Wildlife Service; 4401 N. Fairfax Drive, Suite 222; Arlington,
VA 22203.
We will not accept e-mail or faxes. We will post all comments on
https://www.regulations.gov. This generally means that we will post any
personal information you provide us (see the Public Comments section
below for more information).
FOR FURTHER INFORMATION CONTACT: Adam Zerrenner, Field Supervisor, U.S.
Fish and Wildlife Service, Austin Ecological Services Office, 10711
Burnet Road, Suite 200, Austin, TX 78758; telephone 512/490-0057,
extension 248; fascimilie 512/490-0974.
SUPPLEMENTARY INFORMATION:
Public Comments Solicited
We intend for any final action resulting from this proposal to be
as accurate as possible. Therefore, we solicit data, comments, or
suggestions from the public, other concerned government agencies, the
scientific community, industry, Tribes, or any other interested party
concerning this proposed rule. We particularly seek comments and
information concerning: (1) Information about any threat (or lack
thereof) to the brown pelican; (2) additional information concerning
the range, distribution, location of any additional populations, and
population size of this species; (3) information on habitat destruction
and/or preservation in relation to brown pelicans; (4) impacts to the
species from commercial fisheries outside of the U.S.; (5) current or
planned activities in the species' habitat and the possible impacts to
this species; (6) data on population trends; (7) data on the status of
brown pelicans in the West Indies; (8) data suggesting that any of the
subspecies of brown pelican require protection; and (9) information
pertaining to the requirement for post delisting monitoring. In
addition, because we have received information indicating that one of
the subspecies of brown pelican discussed in this proposal, Pelecanus
occidentalis thagus, may be considered a full species, we request any
additional information regarding brown pelican taxonomy. Please note
that as we make our determination, we will note but not consider
comments merely stating support or opposition to the actions under our
consideration without providing supporting information because section
4(b)(1)(A) of the Act (16 U.S.C. 1531 et seq.) directs that we make
determinations as to whether any species is a threatened or endangered
species ``solely on the basis of the best scientific and commercial
data available.''
You may submit your comments and materials concerning this proposed
rule by one of the methods listed in the ADDRESSES section. Comments
must be submitted to https://www.regulations.gov before midnight
(Eastern Standard Time) on the date specified in the DATES section. We
will not accept comments sent by e-mail or fax or to an address not
listed in the ADDRESSES section. We will not accept anonymous comments;
your comment must include your first and last name, city, State,
country, and postal (zip) code. Finally, we will not consider hand-
delivered comments that we do not receive, or mailed comments that are
not postmarked, by the date specified in the DATES section.
We will post your entire comment--including your personal
identifying information--on https://www.regulations.gov. If you provide
personal identifying information in addition to the required items
specified in the previous paragraph, such as your street address, phone
number, or e-mail address, you may request at the top of your document
that we withhold this information from public review. However, we
cannot guarantee that we will be able to do so.
Comments and materials we receive, as well as supporting
documentation we used in preparing this proposed rule, will be
available for public inspection on https://www.regulations.gov, or by
appointment, during normal business hours, at the U.S. Fish and
Wildlife Service, Austin Ecological Services Office (see FOR FURTHER
INFORMATION CONTACT).
The Act provides for a public hearing on this proposed delisting,
if requested. Requests must be received within 45 days of the date of
publication of this proposal. Such requests must be made in writing and
addressed to Adam Zerrenner, Field Supervisor, U.S. Fish and Wildlife
Service, Austin Ecological Services Office (see FOR FURTHER INFORMATION
CONTACT).
Background
Currently listed brown pelican populations 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; along the Pacific Coast from British Columbia, Canada, south
through Mexico into Central and South America; and in the West Indies,
but are occasionally sighted throughout the U.S. (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 still occurs
throughout its historical range (Shields 2002, pp. 4-5). This proposed
rule includes relevant biological and life history information for the
brown pelican. However, additional information about the brown
pelican's
[[Page 9409]]
biology and life history can be found in the Birds of North America,
No. 609 (Shields 2002, pp. 1-36).
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. Taxonomy of the brown pelican subspecies has not been
critically reviewed for many years, and the classification followed by
the American Ornithological Union (AOU 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.
This proposed delisting rule applies to the entire listed species,
which includes all brown pelican (Pelecanus occidentalis) subspecies.
For a review of the brown pelican's status, see the ``Population
Estimates'' section below. For a review of the threats in relation to
the species status, see the ``Summary of Factors Affecting the
Species'' section below.
Previous Federal Action
Due to population declines of brown pelicans, in 1970, we listed
the species as endangered under the Endangered Species Conservation Act
of 1969 (Pub. L. 91-135, 83 Stat. 275). Brown pelicans were included in
the List of Threatened and Endangered Foreign Species on June 2, 1970
(35 FR 8495), and included in the United States list of endangered and
threatened species on October 13, 1970 (35 FR 16047). The species was
subsequently listed under the Endangered Species Act (Act) of 1973, as
amended (16 U.S.C. 1531 et seq.).
On February 4, 1985, the Service delisted the brown pelican in
Alabama, Florida, Georgia, South Carolina, North Carolina, and points
northward along the Atlantic Coast (50 FR 4938). However, the brown
pelican continued to be listed as endangered throughout the remainder
of its range, including Mississippi, Louisiana, Texas, California,
Mexico, Central and South America, and the West Indies.
On July 5, 1994, we received a petition dated February 21, 1994,
from Joe L. Herring, Secretary, Department of Wildlife and Fisheries,
State of Louisiana, requesting the Service remove the brown pelican
from the List in Louisiana. The petition contained information on
successful pelican reintroductions, colony expansions, population
numbers, and productivity in Louisiana. We were not able to act on the
request, since the processing of delisting actions was assigned the
lowest priority in the allocation of available funding appropriations,
as described in the Federal Register (61 FR 64475; December 5, 1996).
In 1999, delisting actions were moved from the Service's listing
program to the recovery program, allowing us to address requests and
petitions to downlist and delist species. This proposed rule
constitutes our 90-day and 12-month findings for the Louisiana petition
to delist the brown pelican.
On December 14, 2005, we received a petition from Craig Harrison,
of the law firm Hutton and Williams, representing the Endangered
Species Recovery Council, to remove the California brown pelican, the
subspecies of brown pelican occurring along the Pacific Coast of
California and Mexico, including the Gulf of California, from the List.
We note that the taxon on the List is Pelecanus occidentalis, and the
petition is specifically for the delisting of the California brown
pelican subspecies, Pelecanus occidentalis californicus. The petition
contained information on population size, trends, reproduction, and
distribution of the California brown pelican, including information on
the status and management of the species in Mexico. It contained
information on the elimination (e.g., banning of DDT) or management of
threats that originally resulted in the brown pelican being listed as
endangered. On May 24, 2006 (71 FR 29908), we published a notice
announcing our 90-day finding for the petition, in which we concluded
that the petition presented substantial scientific or commercial
information indicating that the petitioned action may be warranted. We
then initiated a 12-month status review of the California brown pelican
to determine if delisting under the Act is warranted. This proposed
rule constitutes our 12-month finding for the petition to delist the
California brown pelican.
On May 24, 2006, we also published a notice announcing initiation
of a 5-year review on the rangewide status of the brown pelican (71 FR
29908). Under the Act, we are required to review listed species at
least once every 5 years and determine whether or not any species
should be removed from the List, or reclassified from endangered to
threatened or from threatened to endangered. The conclusion of this
review, which was based on the best available scientific information,
indicates the currently listed brown pelican population does not meet
the definition of an endangered or threatened species under the Act
(Service 2007a, p. 46).
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, and because 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 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 non-breeding birds as well.
However, the information does indicate the broad distribution of the
species and reflects the large global population estimate of over
620,000 birds, which does not include birds along the Atlantic coast of
the U.S.,
[[Page 9410]]
Florida or Alabama (Service 2007a, pp. 44-45).
Gulf of Mexico Coast
Mississippi--Brown pelicans are currently not known to breed in
Mississippi, but the Great Backyard Bird Count (GBBC) has documented
brown pelicans annually in Mississippi since 1999 (GBBC 2007, pp. 1-9).
In 2003 and 2004, 244 and 261 pelicans, respectively, were counted.
There was an increase to 403 pelicans in 2005, but a large decrease to
54 in 2006 (GBBC 2007, pp. 5-8), which coincides with Hurricane
Katrina. However, in 2007, 334 brown pelicans were documented (GBBC
2007, p. 9).
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, p. 1, 4). 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. Numbers of successful nests are not directly comparable
to numbers of individuals in historic estimates because they do not
account for immature or non-breeding 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) 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, p. 2-3). The highest count was in 2005 with
4,097 breeding pairs in 12 colonies (Service 2006, p. 2). This number
equates to 8,194 breeding birds, which is substantially greater than
historical population estimates for Texas. Numbers declined slightly in
2006 to 3,801 breeding pairs in six nesting colonies (7,602 breeding
birds) (Service 2006, p. 2), possibly due to hurricanes in 2005 (see
discussion of storm effects under Factor A), but they remained above
historical estimates. The 2006 census numbers may be low because survey
data appear to be missing for Sundown Island, which traditionally
supports a large brown pelican breeding colony. There were 1,676
breeding pairs nesting at Sundown Island in 2007 (Erfling 2007a, p. 1;
https://www.sundownisland.org/default.htm), which is comparable to the
number breeding there in 2005 (Service 2006, p. 2).
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 along this same stretch of
coast conducted in March 1986 counted 2,270 birds, down from 4,250
birds estimated in counts conducted between December 1979 and January
1980 (Blankinship 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. No 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.
West Indies
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. 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.
[[Page 9411]]
Migrants that breed in North America augment local numbers primarily
from November to February.''
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
historic record of nesting.
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 found no breeding pelicans at one site in 2002.
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 (IBAs) 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. See ``Human disturbance of nesting
pelicans'' under Factor A below for discussions of possible reasons for
decline.
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 16-36 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. Acosta-Cruz and Mugica-
Vald[eacute]s (2006, p. 65) estimate the population of brown pelicans
in Cuba falls within the range on 1,000 to 4,999 birds and that the
population trend is stable.
Summary of West Indies--Although we do not have detailed
information on brown pelicans throughout the islands of the West
Indies, the distribution of current breeding colonies reported by
Collazo et al. (2000, p. 42) is similar to that reported by van Halewyn
and Norton (1984, pp. 174-175, 201). Estimates of number of breeding
pairs differ between the two reports but the studies differed somewhat
in the sites reported and neither provided detailed methods for their
estimates. Neither Collazo et al. (2000, p. 63) nor van Halewyn and
Norton (1984, pp.174-175, 201) provided estimates for birds nesting in
Cuba, but Acosta-Cruz and Mugica-Vald[eacute]s (2006, p. 65) estimate
the population in Cuba falls within the range on 1,000 to 4,999 birds.
Caribbean and Atlantic Coast of Mexico, Central 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 6200 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 (Blankinship
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 (Blankinship 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 (pp. 144-149)
variously report brown pelicans as: ``Common: high density, likely to
be seen many places,'' ``Transient, present briefly as migrant,''
``Resident, species present all year,'' ``apparently secure in
Belize.'' Brown pelicans are also reported in one reference as nesting
on several cays, 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 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 in Panama, 582 brown pelicans were counted
(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 Humedales costeros de La
Guajira (coastal wetlands of La Guajira). However, no estimate of
numbers of breeding birds was given.
[[Page 9412]]
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 1700 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 non-breeding
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.
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 71,200 nesting pairs, which equates to 142,400 breeding
birds (Henny and Anderson 2007, p. 9). 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 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). 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 3,650
breeding pairs, the Gulf of California population is estimated at
42,970 breeding pairs, and the mainland Mexico population has about
12,880 breeding pairs (Anderson 2007b; Henny and Anderson 2007, p. 9).
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 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, p. 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 non-breeding 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 non-breeding 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 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
Bola[ntilde]os 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 1,976 nest numbers from Coiba Island (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.
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
[[Page 9413]]
birds. Santander et al. (2006, p. 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 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 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.
Summary--Global Population Estimates
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. 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. However, because these estimates are the best available
information, we attempted to use some conservative assumptions in
tabulating these data in order to make a conservative estimate of the
global population size of the brown pelican (Service 2007a, pp. 43-45
and 60-62). This total, or global estimate, is for the listed brown
pelican, which does not include the Atlantic coast of the U.S.,
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 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 U.S., 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 non-breeders 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).
Recovery plans are not regulatory documents and are instead
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. 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. In that instance, the Service may judge that, overall,
the threats have been minimized sufficiently and the species is robust
enough to justify reclassifying the species from endangered to
threatened or perhaps delisting 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. Analyzing the degree of recovery of a species is
also an adaptive management process that may or may not fully follow
the guidance provided in a recovery plan. 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
delisted populations and the currently listed Texas, Louisiana, and
Mississippi populations, 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). The recovery plan
states a general objective to re-establish 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. As of 2005 (prior to Hurricanes Katrina
and Rita), 11 sites in Louisiana were being used for nesting by brown
pelicans: Brush Island, Martin Island, North Island, Pelican Point,
West Breton Island, Baptiste Collette, Queen Bess Island, Wine Island,
Raccoon Island, Rabbit
[[Page 9414]]
Island, and Shallow Bayou. This list includes 7 previously unknown
sites (Hess and Linscombe 2006, pp. 1-4, 7-8). In 2006, nesting
occurred at 15 sites that included the previously mentioned 11.
Hurricane-caused habitat degradation forced many birds to seek out new
nesting locations including three additional sites in the Pelican Point
area, and one on East Queen Bess Island (Hess and Linscombe 2007, pp.
1, 3). As of 2006, 12 sites in Texas were being used for nesting by
brown pelicans: Marker 52 Spoil Island, North Deer Island, Evia Island,
Sunfish Island, Shamrock Island, Deadman Islands, South Pass Islands A
and B, Pelican Island, Sundown Island, Little Pelican Island, and
Dressing Point (Service 2006, p. 2). 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 support 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 (2,289 compared to 593
individuals). 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 appropriate for
determining whether the brown pelican is recovered globally. The second
recovery criterion is the more important of the two 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.
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, p. 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 species' 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 for the subspecies to be
considered for delisting: (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 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.
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, the productivity criterion for
delisting, while it has improved greatly since the time of listing and
has neared the criterion for delisting a few times, 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
[[Page 9415]]
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 reached, reproduction has been sufficient to
maintain a stable population for over 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 and that current productivity is
sufficient to maintain a viable population of brown pelicans.
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 all together. No
subsequent revisions have been made to any of these original recovery
plans. No single recovery plan covers the entire range of the species,
and the remainder of the range outside the U.S., including Central
America, South America, and most of the West Indies is not covered by a
recovery plan. Thus, these focus areas for recovery, which do not have
formal or regulatory distinction, are outdated. 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 proposal is based largely on the analysis of threats in
our recently completed 5-year review (Service 2007a, pp. 1-66). This
review is available at https://ecos.fws.gov/docs/five_year_review/
doc1039.pdf.
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 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. 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 brown pelican's range in danger of extinction or likely to
become endangered within the foreseeable future.
As discussed below in our analysis of factors affecting the
species, we do not foresee any changes in the current protections for
brown pelican. For example, we do not expect any significant changes to
current non-Endangered Species Act habitat protections, regulations
affecting pesticide use and licensing, the Migratory Bird Treaty Act,
Magnuson-Stevens Fishery Conservation and Management Act, or the global
Stockholm Convention on Persistent Organic Pollutants. We could
consider that many of these protections would remain in place in
perpetuity. However, considering this as a timeframe for analysis could
introduce a considerable level of uncertainty and it may not be
reasonable to assume that we can project an analysis out in perpetuity.
Therefore, for the purposes of our analysis, we considered as a lower
bound the timeframe over which it would be reasonable to expect
population level or demographic effects of threats to be detected and
to put the species at risk of becoming endangered. Factors most likely
to affect population levels and key demographic characteristics of
brown pelicans include those that affect reproduction over a period of
several years, and include factors such as disturbance of nest sites,
contaminants, and availability of prey. Therefore, for the purposes of
this proposed rule, we consider ``foreseeable future'' for the brown
pelican at a minimum to be 30 years, since it is a reasonable timeframe
for analysis of factors identified that could affect the species in the
future and as they relate to brown pelican biology. While average life
spans are not known, fewer than 2 percent are thought to live past 10
years of age, and the oldest known individual was 43 years old
(Schreiber and Mock 1988, p. 178). Additionally, since age at first
nesting is generally 3 to 5 years (Shields 2002, p. 18), the average
brown pelican breeds at 4 years of age, thereby replacing itself within
8 years. Therefore, 30 years, which incorporates one long life cycle
and 10 possible generations, represents a reasonable biological
timeframe to determine if threats could be significant.
The following analysis examines all five factors currently
affecting, or that are likely to affect, the brown pelican distribution
that is currently listed within the foreseeable future.
[[Page 9416]]
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, predator-free coastal
islands. 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;
Jim[eacute]nez 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 off-shore 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., Launcularia 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 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 and protection 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, p. 1097-1099;
Anderson 2007a), 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