Overview
Wood
storks are large wading
birds approximately 3 1/2 feet in height
with a wing span
of over 5 feet. They are distinguished by a dark
unfeathered head
and neck, a white body, and a black tail and wing
tips
. Like most other wading birds, wood storks feed
on small fish
in shallow freshwater
wetlands. They use tall cypresses near the
water for colonial
nest
sites.
Wood storks (Mycteria americana) are one of two species of
storks that breed
in North America. This large, long-legged inhabitant
of marshes, cypress swamps
, and mangrove swamps reaches
the northern
limit
of its breeding range
in the southeastern U.S., where it breeds
in colonies with great egrets, snowy egrets, white ibises, and many
other species. The unique feeding method of the wood stork gives
it specialized habitat
requirements; the habitats on which wood storks
depend have been disrupted by changes in the distribution, timing,
and quantity
of water flows
in South Florida. The population declines
that accompanied this disruption led to its listing as an endangered
species and continue to threaten the recovery of this species in
the U.S.
Interesting Facts
Common Names
Click on the language to view common names.
Common Names in Czech:
Nesyt Americk
Common Names in Danish:
Amerikansk Skovstork
Common Names in Dutch:
Kaalkopooievaar
Common Names in English:
American jabiru, American Wood Ibis, American wood stork, flinthead, Gannet, gourdhead, Hammerhead, ironhead, preacher, Spanish buzzard, wood ibis, wood stork
Common Names in Estonian:
Muda-Toonekurg
Common Names in Finnish:
Amerikaniibishaikara
Common Names in French:
Cigogne Am, Tantale D'am, tantale d'amërique
Common Names in German:
Amerikanischer Nimmersatt, Waldstorch
Common Names in Guarani:
Tujuju Kangy
Common Names in Haitian Creole French:
Tantal Rak Bwa
Common Names in Italian:
Cicogna Americana, Tantalo Americano
Common Names in Japanese:
Amerikatokikou, アメリカトキコウ
Common Names in Latin:
Mycteria americana
Common Names in Norwegian:
Amerikastork
Common Names in Polish:
Dlawigad Amerykanski
Common Names in Portuguese:
Cabe
Common Names in Portuguese (Brazil):
Cabe
Common Names in Russian:
Аист лесной, американский клювач
Common Names in Slovak:
Bocian Lesn
Common Names in Spanish:
Cayama, Cig, Cigüeña americana, T
Common Names in Spanish (Argentine):
Tuyuy
Common Names in Spanish (Bolivia):
Tuyuy
Common Names in Spanish (Costa Rica):
Cigue
Common Names in Spanish (Cuba):
Cayama
Common Names in Spanish (Dominican Republic):
Coco
Common Names in Spanish (Honduras):
Cig
Common Names in Spanish (Mexico):
Cigue
Common Names in Spanish (Nicaragua):
Cig
Common Names in Spanish (Paraguay):
Tuyuy
Common Names in Spanish (Uruguay):
Cig
Common Names in Swedish:
Amerikansk Ibisstork
Description
Physical Description
Adult : Head : bare, dirty brownish-black Bill: blackish Curvature: decurved Length : long Shape : thick heavy bill drooped at tip Neck: bare, dirty brownish-black Body: white Legs : Foot Color: blackish Leg Color: blackish gray Wings : Flight Feathers: black Secondaries: black Tail: black.Immature: Head: grayish down Bill: horn color or yellowish Curvature: decurved Length: long Shape: thick heavy bill drooped at tip Neck: grayish down Body: dull white Legs: Foot Color: blackish Leg Color: blackish gray Wings: Secondaries: black.
Color:
White body. Black tail, legs
, and flight feathers.
Adult
: Dark bill
Immature
: Yellow bill · Feathered head
is grayish-brown
Size/Age/Growth
About 35 to 45 inches long, with a wingspan of 65 to 65 inches. Adults weigh about 96 ounces .
Habitat
The wood
stork is primarily associated with freshwater
and estuarine
habitats
for nesting, roosting, and foraging
. Wood storks typically
construct their nests
in medium to tall trees
that occur in stands
located either in swamps
or on islands surrounded by relatively broad
expanses of open water
(Palmer 1962, Rodgers et al.
1996, Ogden 1991).
Historically, wood storks in South Florida established
breeding colonies
primarily in large stands of bald
cypress (Taxodium distichum) and
red mangrove
(Rhizophora mangle). The large, historic Everglades
NP nesting colonies were in estuarine zones. These estuarine zones
are also an important feeding habitat for the nesting birds. In one
study of wood stork nesting throughout Florida, which was conducted
prior to the 1960s, more than half of all wood stork nests were located
in large bald cypress stands, 13 percent were located in red mangrove,
eight percent in partially harvested bald cypress stands, six percent
in dead oaks (Quercus spp.
), and five percent in small pond
cypress
(T. distichum var. nutans) (Palmer 1962). Wood storks have also been
observed constructing their nests in custard (pond) apple (Annona
glabra), black gum (Nyssa biflora), buttonwood (Conocarpus erectus),
black mangrove (Avicenna germinans), strangler fig (Ficus aurea),
and southern willow (Salix carolina). Coastal nest sites occur in
red mangroves and, occasionally, Brazilian pepper (Schinus terebinthifolius),
cactus (Opuntia stricta), and Australian
pine (Casuarina equisetifolia).
During the nonbreeding season
or while foraging, wood storks occur
in a wide variety of wetland habitats. Typical foraging sites for
the wood stork include freshwater marshes and stock ponds
, shallow,
seasonally flooded roadside or agricultural ditches, narrow tidal
creeks
or shallow tidal pools, managed impoundments
, and depressions
in cypress heads
and swamp sloughs. Because of their specialized
feeding behavior, wood storks forage
most effectively in shallow-water
areas with highly concentrated prey
(Ogden et al. 1978, Browder 1984,
Coulter 1987). In South Florida, low, dry-season water levels are
often necessary to concentrate
fish to densities suitable for effective
foraging by wood storks (Kahl 1964, Kushlan et al. 1975). As a result,
wood storks will forage in many different shallow wetland depressions
where fish become concentrated, either due to local reproduction
by fishes
, or as a consequence of seasonal drying.
The loss or degradation of wetlands in central and South Florida
is one of the principal threats
to the wood stork. Nearly half of
the Everglades has been drained for agriculture and urban development
(Davis and Ogden 1994). The Everglades Agricultural Area (EAA) alone
eliminated 802,900 ha of the original Everglades, and the urban areas
in Miami-Dade, Broward and Palm Beach
counties have contributed to
the loss of spatial extent of wood stork habitat. Everglades NP has
preserved only about one-fifth of the original extent of the Everglades,
and areas of remaining marsh
outside of the Everglades NP have been
dissected
into impoundments of varying depths.
The U.S. Army
Corps of Engineers (COE) Central and Southern Florida
(C and SF) Project encompasses 4,660,000 ha from Orlando to Florida
Bay
and includes about 1,600 km
each of canals and levees
, 150 water
control structures, and 16 major pump stations
. This system
has disrupted
the volume, timing, and direction
of fresh water
flowing through
the Everglades. The natural sheet flow
pattern
under which the Everglades
evolved since about 5,000 years ago has not existed for about 75
years (Leach et al. 1972, Klein et al. 1974). The diversion of natural
sheet flow to canals, the loss of fresh water to seepage and to pumping
to tidal waters, and the extraction of fresh water for irrigation
and urban water supply has led to saltwater
intrusion in coastal
counties from St
. Lucie County on the east coast to Sarasota County
on the west coast.
Although the major drainage
works completed the conversion of wetlands
to agriculture in the EAA by about 1963, loss of wetlands continues
to the present at a slower, but significant rate. In the entire State
of Florida between the mid-1970s to the mid-1980s, 105,000 ha of
wetlands (including marine
and estuarine offshore habitats) were
lost; we do not have an estimate for freshwater wetlands in central
and south Florida (Hefner et al. 1994).
Vegetation: freshwater marshes, saltwater and brackish marshes, freshwater lakes and ponds • Maximum Elevation: 800 meters • Foraging Strata: Water • Center of Abundance: Lower tropical: lowlands, lower than 500 m.; tropics. • Sensitivity to Disturbance: Low
Typically found at an altitude of 0 to 2,911 meters (0 to 9,551 feet).[1]
Ecology:
List of Habitats
:
- 1 Forest
- 1.7 Forest - Subtropical/Tropical Mangrove Vegetation Above High Tide Level
- 4 Grassland
- 4.6 Grassland - Subtropical/Tropical Seasonally Wet/Flooded
- 5 Wetlands (inland)
- 5.4 Wetlands (inland) - Bogs , Marshes, Swamps , Fens , Peatlands
- 5.5 Wetlands (inland) - Permanent Freshwater Lakes (over 8ha)
- 12 Marine Intertidal
- 12.5 Marine Intertidal - Salt Marshes (Emergent Grasses)
- 15 Artificial/Aquatic & Marine
- 15.9 Artificial/Aquatic - Canals and Drainage Channels , Ditches
Biology
Diet
Wood
storks use a specialized feeding behavior called tactolocation,
or grope feeding. A foraging
wood stork wades through the water with
its beak
immersed
and partially open (7 to 8 cm). When it touches
a prey
item, a wood stork snaps its mandibles shut, raises its head
,
and swallows what it has caught (Kahl 1964). Regularly, storks will
stir the water with their feet, a behavior which appears to startle
hiding prey (Rand 1956, Kahl 1964, Kushlan 1979). Tactolocation allows
storks to feed
at night and use water that is turbid
or densely vegetated.
However, the prey must be concentrated in relatively high densities
for wood storks to forage
effectively. The natural hydrologic regime
in South Florida involves seasonal flooding of extensive areas of
the flat, low-lying peninsula, followed by drying events which confine
water to ponds
and sloughs
. Fish populations reach high numbers during
the wet season
, but become concentrated into smaller areas as drying
occurs. Consumers
, such as the wood stork, are able to exploit
high
concentrations of fish in drying pools and sloughs. In the pre-drainage
Everglades
, the dry season of South Florida provided wood storks
with ideal foraging conditions by concentrating prey species in gator
holes
and other drainages
in the Everglades basin
. In coastal areas,
the tidal
cycle strongly influences use of saltwater
habitats
by
wood storks. The relatively great tidal amplitudes characteristic
of coastal marshes in northeast Florida, Georgia, and South Carolina
serve to concentrate
prey. similarly to the seasonal drawdowns
found
in freshwater
systems
(FWS 1997).
Storks forage in a wide variety of shallow wetlands, wherever prey
reach high enough densities, and in water that is shallow and open
enough for the birds to be successful in their hunting efforts
(Ogden
et al.
1978, Browder 1984, Coulter 1987). Good feeding conditions
usually occur in relatively calm water, where depths are between
10 and 25 cm, and where the water column
is uncluttered by dense
patches of aquatic
vegetation (Coulter and Bryan 1993). In South
Florida, dropping water levels are often necessary to concentrate
fish to suitable densities (Kahl 1964, Kushlan et al. 1975). In east-central
Georgia, where stork prey is almost twice as large as the prey in
Florida, wood storks feed where prey densities are significantly
lower than foraging sites in Florida (Coulter 1992, Coulter and Bryan
1993, Depkin et al. 1992). Typical foraging sites throughout the
wood storks range
include freshwater marshes and stock ponds
, shallow,
seasonally flooded roadside or agricultural ditches, narrow tidal
creeks
or shallow tidal pools, managed impoundments
, and depressions
in cypress heads and swamp
sloughs. Almost any shallow wetland depression
that concentrates fish, either through local reproduction
or the
consequences of area drying, may be used as feeding habitat.
Wood storks feed almost entirely on fish between 2 and 25 cm in length
(Kahl 1964, Ogden et al. 1976, Coulter 1987). In South Florida, Ogden
et al. (1976) found that certain fish species were taken preferentially.
Mosquito fish (Gambusia affinis
) were under represented in the diet
in proportion to abundance
, whereas, flagfish (Jordanella floridae),
sailfin mollies (Poecilia latipinna), marsh
killifish (Fundulus confluentus),
yellow bullheads (Ictalurus natalis), and sunfish (Centrarchidae)
were over represented. Wood storks also occasionally consume crustaceans,
amphibians
, reptiles
, mammals, birds, and arthropods
. Fish densities
at stork foraging sites varied from 15.6 individuals/m2 in east-central
Georgia to 40 individuals/m2 in South Florida (Ogden et al.1978,
Depkin et al. 1992).
Because wood storks rely on concentrated food sources which are patchily
distributed over large areas, they need to be able to find new feeding
grounds
with minimal energy expenditure. Wood storks have soaring
abilities that allow them to reach high altitudes
and many kilometers
without the energy expenditure of wing-flapping. A recent study suggested
that soaring flight by storks can be accomplished at one-tenth the
energetic cost of flapping flight (Bryan and Coulter 1995). The long
distances
they travel, however, shortens the time available to wood
storks for feeding and reduces the number of times an adult
stork
can return to its nest
to feed young (Kahl 1964). During the breeding
season, feeding areas proximal
to wood stork breeding colonies may
play an important role in chick survival and provide enhanced opportunities
for newly fledged birds to learn effective feeding skills.
Reproduction
Mating occurs after a period of highly ritualized courtship
displays
at the nest
site (Kahl 1972). As a female bird approaches, male birds
establish themselves at potential nest sites and perform ritualized
preening behavior. Rival
males will extend their necks, grab their
opponents bills, and clatter their bills loudly a few times. Females
respond by bill gaping and a spread-winged balancing posture. Females
will be turned away initially, but after repeated approaches, will
respond by swaying their heads
, preening, or playing with nearby
twigs
(Kahl 1972). During copulation
, males loudly clatter their
bills. Mated pairs greet each other with exaggerated, mutual up-down
head movements and hissing calls
.
Wood
storks tend to use the same colony
sites over many years, as
long as the sites remain undisturbed and sufficient feeding habitat
remains in the surrounding wetlands. Site turnover rates for the
colonies in South Carolina are very low at 0.17 colonies per year.
Current
year colonies have an 89 percent likelihood of remaining
active
in consecutive years. However, many of these South Carolina
colonies are relatively recent.
Traditional wetland nesting sites may be abandoned by storks once
local or regional drainage
schemes remove surface water from beneath
the colony trees. Maintaining adequate water levels to protect nests
from predation
is a critical factor
affecting production
of a colony.
The lowered water levels allow nest access by raccoons and other
land-based predators
. As a result of such drainages and predation,
many storks have shifted colony sites from natural to managed or
impounded wetlands. The percentage of wood storks that nested in
either altered wetlands (former natural wetlands with impounded water
levels) or artificial wetlands (former upland
sites with impounded
water) in central and north Florida colonies increased from about
10 percent in 1960 to between 60 and 82 percent between 1976 and
1986.
Wood storks are seasonally monogamous, probably forming a new pair
bond every season
. Three and 4-year-old birds have been documented
to breed
, but the average age of first breeding is unknown. Once
wood storks reach sexual maturity they are assumed to nest every
year; there are no data
on whether they breed for the remainder of
their life or whether the interval between breeding attempts changes
as they age (FWS 1997).
Wood storks construct their nests in trees
that are usually standing
in water or in trees that are on dry land
if the land is a small
island surrounded by water. The nest are large rigid
structures usually
found in the forks of large branches or limbs. Storks may add guano
to the nest to stabilize the twigs. (Rodgers et al.
1988). The nest
may be constructed in branches that are only a meter above the water
or in the tops of tall trees. They construct their nests out of sticks
,
with a lining
of finer material
. Their nests are flat platforms,
up to 1 m
in diameter, and are maintained by the adult
storks throughout
the breeding season
. Although both adults maintain the nest, the
male wood stork usually brings nest material to the female after
they complete
their courtship (Palmer 1962).
The date on which wood storks begin nesting varies geographically.
In Florida, wood storks lay
eggs
as early as October and as late
as June (Rodgers 1990). In general, earlier nesting occurs in the
southern portion of the state (below 27°N). Storks nesting in
the Everglades
and Big Cypress basins
, under pre-drainage conditions
(1930s to 1940s), formed colonies between November and January (December
in most years) regardless of annual
rainfall and water level conditions
(Ogden 1994 and 1998). In response to deteriorating habitat conditions
in South Florida, wood storks in these two regions have delayed the
initiation of nesting, approximately two months, to February or March
in most years since the 1970s. This shift in the timing of nesting
is believed to be responsible for the increased frequencies of nest
failures and colony abandonment in these regions over the last 20
years; colonies that start after January in South Florida risk having
young in the nests when May-June rains flood marshes and disperse
fish.
Female wood storks lay a single clutch
of eggs per breeding season.
However, they will lay a second clutch if their nests fail early
in the breeding season (M.
Coulter 1996). Wood storks lay two to
five (usually three) eggs depending on environmental conditions
;
presumably larger clutch size in some years are responses to favorable
water levels and food resources
. Once an egg has been laid in a nest,
one member
of the breeding pair never leaves the nest unguarded.
Both parents are responsible for incubation
and foraging
(Palmer
1962). Incubation takes approximately 28 days, and begins after the
first one or two eggs are laid; therefore egg-hatching is asynchronous.
Younger, smaller chicks are often the first to die during times of
food stress (FWS 1997). It takes about 9 weeks for the young to fledge
;
once they fledge, the young stay
at the nest for an additional 3
to 4 weeks to be fed by their parents. Parents feed
the young nestlings
by regurgitating whole fish
into the bottom
of the nest; parents
feed the young three to 10 or more times per day. Larger nestlings
are fed directly bill to bill. Feedings tend to be more frequent
when young are small. Ogden et al. (1978) reported that only one
to two feedings per day, per nest, have been recorded in South Florida
colonies when adults were forced to fly great distances
to locate
prey
. Kahl (1964) calculated that an average wood stork family
(two
adults and two nestlings) requires 201 kg
(443 lbs
) of fish during
a breeding season, and that a colony of 6,000 nests therefore requires
1,206,000 kg of fish during the breeding season. A similar calculation
for a typical Everglades NP or Corkscrew Swamp
colony with 200 nests
would require 40, 200 kg (88,600 lbs) of fish during the breeding
season.
The production of wood stork colonies varies considerably between
years and locations, apparently in response to differences in food
availability; colonies that are limited by food resources may fledge
an average of 0.5 to 1.0 young per active nest; colonies that are
not limited by food resources may fledge between 2.0 and 3.0 young
per active nest (Ogden 1996a).
Migration
Nonmigratory. During the non-breeding season (the summer to fall rainy season in South Florida), juvenile wood storks from South Florida colonies have been located throughout the Florida peninsula, southern Georgia, coastal South Carolina, central Alabama, and east-central Mississippi (Ogden 1996a). Additionally, marked individuals from a colony in east-central Georgia were found in the central Everglades during the winter. This information suggests that the southeastern population of wood storks is a single population that responds to changing environmental conditions through temporal relocation. Rodgers (1996) data analysis of genetic variation in wood stork populations in South Florida, central Florida, north Florida, Georgia, and South Carolina support this evaluation.
Taxonomy
- Domain:
Eukaryota
(
)
- Whittaker & Margulis,1978
- eukaryotes
- Kingdom:
Animalia
(
)
- C. Linnaeus, 1758
- animals
- Subkingdom:
Bilateria
(
)
- (Hatschek, 1888) Cavalier-Smith, 1983
- Branch:
Deuterostomia
(
)
- Grobben, 1908
- Infrakingdom:
Chordonia
(
)
- (Haeckel, 1874) Cavalier-Smith, 1998
- Phylum:
Chordata
(
)
- Bateson, 1885
- Chordates
- Subphylum:
Vertebrata
(
)
- Cuvier, 1812
- Infraphylum:
Gnathostomata
(
)
- auct.
- Jawed Vertebrates
- Superclass:
Tetrapoda
(
)
- Goodrich, 1930
- Class:
Aves
(
)
- Linnaeus, 1758
- Subclass:
Avialae
(
)
- Gauthier, 1986
- Infraclass:
Aves
(
)
- (C. Linnaeus, 1758)
- Cohort:
Neognathae
(
)
- Pycraft, 1900
- Superorder:
Ciconiimorphae
(
)
- Garrod, 1874
- Order:
Ciconiiformes
(
)
- Bonaparte, 1854
- Suborder:
Ciconiae
(
)
- Bonaparte, 1854
- Infraorder:
Ciconiides
(
)
- Parvorder:
Ciconiida
(
)
- Superfamily:
Ciconioidea
(
)
- Sundevall, 1836
- Family:
Ciconiidae
(
)
- Sundevall, 1836
- Subfamily:
Ciconiinae
(
)
- Genus:
Mycteria
(
)
- C. Linnaeus, 1758
- Specific name:
americana
- Linnaeus 1758
- Scientific name: - Mycteria americana Linnaeus, 1758 Linnaeus 1758
- Specific name:
americana
- Linnaeus 1758
- Genus:
Mycteria
(
- Subfamily:
Ciconiinae
(
- Family:
Ciconiidae
(
- Superfamily:
Ciconioidea
(
- Parvorder:
Ciconiida
(
- Infraorder:
Ciconiides
(
- Suborder:
Ciconiae
(
- Order:
Ciconiiformes
(
- Superorder:
Ciconiimorphae
(
- Cohort:
Neognathae
(
- Infraclass:
Aves
(
- Subclass:
Avialae
(
- Class:
Aves
(
- Superclass:
Tetrapoda
(
- Infraphylum:
Gnathostomata
(
- Subphylum:
Vertebrata
(
- Phylum:
Chordata
(
- Infrakingdom:
Chordonia
(
- Branch:
Deuterostomia
(
- Subkingdom:
Bilateria
(
- Kingdom:
Animalia
(
Notes
Name
Status: Accepted Name
.
Last scrutiny: 17-Oct-2001
Similar Species
Great Egret, American White Pelican, White Ibis
Members of the genus Mycteria
ZipcodeZoo has pages for 5 species and subspecies in this genus:
M. americana (American Wood Stork) · M. cinerea (Milky Stork) · M. ibis (Yellow-Billed Stork) · M. ibis ibis (Yellow-Billed Stork) · M. leucocephala (Painted Stork)
More Info
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Further Reading
- A Directory of Neotropical Wetlands. IUCN Conservation Monitoring Centre url p. 102, p. 12, p. 13, p. 138, p. 145, p. 179, p. 193, p. 195, p. 205, p. 237, p. 246, p. 249, p. 255, p. 275, p. 283, p. 284, p. 286, p. 287, p. 289, p. 290, p. 293, p. 294, p. 298, p. 299, p. 309, p. 310, p. 312, p. 313, p. 319, p. 321, p. 322, p. 323, p. 324, p. 338, p. 344, p. 345, p. 348, p. 366, p. 367, p. 372, p. 373, p. 374, p. 377, p. 380, p. 381, p. 382, p. 388, p. 389, p. 391, p. 392, p. 393, p. 396, p. 404, p. 407, p. 410, p. 412, p. 414, p. 416, p. 491, p. 55, p. 56, p. 58, p. 672, p. 82, p. 88, p. 91, p. 99.
- A check list of North American birds. Boston: Estes and Lauriat, 1882. url p. 106.
- A check list of North-American birds by Elliott Coues. Salem, Mass.: F.W. Putnam, 1879. url .
- A checklist of the vertebrate animals of Kansas / George D. Potts, Joseph T. Collins. [Lawrence, Kan.]: Museum of Natural History, University of Kansas, 1991. url p. 7.
- A contribution to the ornithology of northeastern Brazil, by Charles E. Hellmayr. 12 1929 Chicago, 1929. url p. 485.
- A dictionary of birds, by Alfred Newton, assisted by Hans Gadow, with contributions from Richard Lydekker. .. Charles S. Roy. .. and Robert W. Shufeldt. .. London, A. and C. Black, 1893-1896. url p. 462, p. 462.
- A distributional list of the birds of Montana, with notes on the migration and nesting of the better known species, by Aretas A. Saunders. Berkeley, Calif., The Club, 1921. url p. 190, p. 42.
- A faunal investigation of Long Point and vicinity, Norfolk County, Ontario / [Toronto: Royal Ontario Museum of Zoology], 1931. url p. 222.
- A flying trip to the tropics. A record of an ornithological visit to the United States of Colombia, South America and to the island of Curaao, West Indies, in the year 1892, Cambridge [Mass.]Riverside press, 1895. url p. 126.
- A history of the birds of Colorado, London, Witherby & Co., 1912. url , .
- A list of the genera of birds: with their synonyma and an indication of the typical species of each genus / by George Robert Gray. London: Printed and sold by R. and J.E. Taylor, 1841. url p. 87.
- A manual of North American birds. Philadelphia, Lippincott, 1887. url .
- A study of the structure of feathers, with reference to their taxonomic significance, by Asa C. Chandler. Berkeley, University of California press, 1916. url p. 318, p. 320, p. 412.
- A survey of natural areas in Brunswick County, North Carolina: for The North Carolina Natural Heritage Program, Coastal Natural Area Inventory Project / Raleigh: North Carolina Coastal Energy Impact Program, Office of Coastal Management, North Carolina Dept. of Natural Resources and Community Development, [1982?] url , .
- A systematic list of the birds of California / by Joseph Grinnell. Hollywood: Cooper Ornithological Club, 1912. url p. 8.
- Abstract of the proceedings of the Linnaean Society of New York. [New York]: The Society, [1889-1932]. url p. 111, p. 83.
- American bird magazine, ornithology. Worcester, Mass.: C.K. Reed, 1903-1906. url p. 214.
- American ornithology, for home and school. [Worcester, Mass.: Charles K. Reed], 1901-[1906]. url p. 214.
- An account of the mammals and birds of the lower Colorado Valley: with especial reference to the distributional problems presented / by Joseph Grinnell. Berkeley, Calif.: University of California Press, 1914. url p. 110, p. 116.
- Animal life and the world of nature: a magazine of natural history throughout the world. London: Hutchinson, 1902-1904. url , p. 398.
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Notes
Contributors
- BirdLife International 2009. Mycteria americana. In: IUCN 2011. IUCN Red List of Threatened Species. Version 2011.2. <www.iucnredlist.org>. Downloadedon 02February2012.
- Brands, S.J. (comp.) 1989-present. The Taxonomicon. Universal Taxonomic Services, Zwaag, The Netherlands. Accessed January 9, 2012.
- IUCN 2012. IUCN Red List of Threatened Species. Version 2011.2. . Downloaded on January 28, 2012.
Data Sources
Accessed through GBIF Data Portal March 09, 2008:
- Avian Knowledge Network: eBird
- Avian Knowledge Network: Great Backyard Bird Count
- Avian Knowledge Network: Project FeederWatch
- Borror Laboratory of Bioacoustics
- Canadian Biodiversity Information Facility: Provincial Museum of Alberta, Edmonton, AB, Canada. Birds (Aves)
- Canadian Biodiversity Information Facility: Royal British Columbia Museum
- Institute of Marine and Coastal Sciences, Rutgers University: Bay of Fundy Species List (OBIS Canada)
- Marine Science Institute, UCSB: Paleobiology Database
- Museum of Vertebrate Zoology: Terrestrial vertebrate specimens
- New Brunswick Museum: NBM birds
- Royal Ontario Museum: Bird specimens
- Santa Barbara Museum of Natural History: Santa Barbara Musem of Natural History
- UCLA-Dickey Bird Collection (UCLA-Dickey): Bird specimens
- UNIBIO, IBUNAM: CNAV/Coleccion Nacional de Aves
Identifiers
- Biodiversity Heritage Library NamebankID: 1
- Catalogue of Life Accepted Name Code: ITS-174897
- Global Biodiversity Information Facility Taxonkey: 2496811
- Integrated Taxonomic Information System (ITIS) Taxonomic Serial Number (TSN): 174897
- IUCN ID: 224827
- Natural Heritage Network Species Identifier: ABNGF02010
- U.S. Fish and Wildlife Service Species Identifier: B06O
- Zipcode Zoo Species Identifier: 913
Footnotes
- Mean = 28.530 meters (93.602 feet), Standard Deviation = 48.460 based on 46,210 observations. Altitude information for each observation from British Oceanographic Data Centre. [back]
