Geographic Range
Audubon’s orioles ( Icterus graduacauda ) are year-round residents of southern Texas, eastern and southern Mexico, and the northern tip of Central America. In Mexico, the range splits into two allopatric regions: the eastern range extends from northeastern Mexico (Tamaulipas and Nuevo Leon) south to central Veracruz; the western range extends from central Nayarit south to Oaxaca. There are also a few populations in Belize.
Audubon’s orioles are further divided into four subspecies:
I. g. graduacauda
,
I. g. audubonii
,
I. g. nayaritensis
and
I. g. dickeyae
. The Atlantic range is occupied by overlapping populations of
I. g. graduacauda
and
I. g. audubonii
, while
I. g. nayaritensis
and
I. g. dickeyae
inhabit the western range. Range overlap is not observed between
I. g. nayaritensis
and
I. g. dickeyae
. The range of
I. g. audubonii
is confined to southern Texas, Tamaulipas, and Nuevo Leon, while
I. g. graduacauda
is found in the Mexican states of Veracruz and San Luis PotosĂ. Sightings of
I. g. dickeyae
have been documented in southern Mexico from Guerrero east to Oaxaca. The subspecies
I. g. nayaritensis
inhabits the western portions of Nayarit and northwestern Jacisco.
- Biogeographic Regions
- nearctic
- neotropical
Habitat
Audubon’s orioles are a tropical species that prefers the edges of dense, established
woodlands and riparian areas (Flood et al., 1990). They are found in a wide range
of woodland habitats including scrubland, cloud forest, and both deciduous and evergreen
forest (Flood et al., 1990; American Ornithologist’s Union, 1998). They are rarely
found in open fields or in urban areas, though they may visit suburban feeding stations
even in winter (Flood et al., 2002). Audubon’s orioles may be found at elevations
of up to 2500 m, but avoid areas below 500 m in elevation (Flood et al., 1990).
- Habitat Regions
- tropical
- terrestrial
- Terrestrial Biomes
- forest
- scrub forest
Physical Description
Audubon’s orioles are medium sized orioles and are nearly monomorphic, though males
are slightly larger and brighter than females (Flood et al., 2002). Measurements range
from 190 to 240 mm in length and average 42 grams in mass (Sibley, 2000), ranging
in mass from 31 to 45 grams (Flood et al., 1990). They are the only yellow-bodied
oriole species with a fully black hood in the New World (Jaramillo and Burke, 1999).
In most cases the edges of the bib are poorly defined. The culmen is stout, black,
and straight. The tail is black and is “long, narrow and obviously graduated” (Jaramillo
and Burke, 1999).
In adult males, the wings and tail are black; wings have white-fringed greater coverts
that form a wing bar (Jaramillo and Burke, 1999). The tail feathers are olive tipped,
lending the tail a “graduated”, or stepped, appearance. The remiges and retrices (flight
feathers) are white fringed. The body is generally yellow and the underparts are brighter
than the back and nape, which are greenish-yellow (Flood et al., 2002). The median
and lesser coverts form yellow epaulets. While it is difficult to determine the sex
of an individual at a distance, adult females of this species are duller than males,
with an olive green wash on the back and wings (Flood et al., 1990). Juvenile Audubon’s
orioles have a pink lower mandible, a “greenish-gray” face, and yellow-tipped gray
wings. Immature individuals resemble females, but have duller wings and greener upperparts
(Jaramillo and Burke, 1999). Species bearing similar plumage include Scott's orioles
(
Icterus parisorum
), Greater Antillean orioles (
Icterus dominicensis
), and black-cowled orioles (
Icterus prosthemelas
). Scott's orioles are distinguished from
I. graduacauda
by their more-prominent wing bars and yellow-fringed retrices; black-cowled orioles
and Greater Antillean orioles are distinguished by the absence of wing bars (Flood
et al., 2002).
Icterus graduacauda plumage varies geographically as described below:
Icterus g. audubonii generally fits the description given above.
Icterus g. graduacauda is smaller and lacks white fringes on the wings and tail.
Icterus g. nayaritensis exhibits a greater degree of sexual dimorphism, males being markedly brighter than females.
Icterus g. dickeyae
is larger and brighter than the other three subspecies, with a cleaner border to
the hood. The epaulets are more restricted, being orange-yellow only on the lesser
coverts. The edges of the wings are yellow and the wing bars are absent. Additionally
there may some black tipping or spotting on the back. Because of the dramatic differences
in plumage, behavior, song, and habitat preference between
I. g. dickeyae
and the other three subspecies currently grouped under
I. graduacauda
, research efforts are considering whether this subspecies should be considered a
separate species.
- Other Physical Features
- endothermic
- homoiothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
- male larger
Reproduction
Audubon’s orioles are monogamous.
- Mating System
- monogamous
Nests of Audubon’s orioles are semi-pensile (dangling) and cup shaped; the nest is built so that it hangs at the rim from a branch. Unlike other closely related species, this species prefers to build its nest close to the trunk rather than on smaller branches. Nests are usually built from between 12.9 to 33 m above the ground in several different species of large trees. In Texas, Audubon’s orioles prefer mesquite trees and make their nests 1.8 to 4.3 m above the ground. Nests are usually constructed of fine plant fibers, primarily from strands of the leaves of palmetto plants (Flood et al., 1990). According to Flood et al. (2002): “Audubon’s oriole nests are small relative to the body size of the birds that built them.”
Breeding occurs during wet seasons and brood sizes range from three to five eggs.
Due to the long breeding season, mating pairs will occasionally attempt to raise a
second brood. Eggs are light blue with evenly distributed dark markings. Occasionally,
eggs have large dark blotches clustered around the broad end of the egg (Jaramillo
and Burke, 1999; Flood et al., 1990).
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
Only females incubate the eggs; both parents however, play a role in the care of the
nestlings, feeding and protecting the young as well as cleaning the nest. A mated
pair will defend the nest against predators and nest parasites, charging and sometimes
striking the target (Flood et al., 2002). Adults remove fecal sacs from the nests,
often eating them (Flood et al., 1990). It takes eleven days for newly hatched Audubon’s
orioles to fledge (Jaramillo and Burke, 1999)
- Parental Investment
-
pre-fertilization
- provisioning
-
protecting
- female
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
-
pre-independence
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
Lifespan/Longevity
Due to a lack of data on this species, longevity is unknown.
Behavior
Audubon’s orioles can usually be seen alone or in pairs. Mated pairs often forage
together. In the winter, Audubon’s orioles may join mixed-species flocks containing
other, similarly sized birds including green jays (
Cyanocorax yncas
), tanagers (
Thraupidae
), and other orioles (
Icterus
) (Flood et al., 2002). Sometimes this species is also seen in small conspecific flocks
of eight to ten individuals (Bendire, 1895; Flood et al., 2002). Audubon’s orioles
seem to be territorial during the breeding season, but do not seem to exhibit this
behavior during the winter months (Flood et al., 2002)
Home Range
Due to a lack of data, the home range size of this species is unknown.
Communication and Perception
Both male and female Audubon’s orioles sing and their song structures seem to be identical. Mated pairs answer each others' calls, possibly to reinforce pair bonding, though not all mated pairs use song extensively (Jaramillo and Burke, 1999). The species overall is less vocal than North American Icterus species (Flood et al., 1990). During the breeding season, mated pairs respond to calls of nearby conspecifics. It is hypothesized that in this species song is used in territory defense (Flood et al., 2002). It is believed that this species sings less frequently during cold weather (Flood et al., 1990). As of 2002, there is no information regarding possible geographic variation in song (Flood et al., 2002).
The Audubon’s oriole voice have been described by as “low, mellow, humanlike whistle”.
It consists of a series of non-repeating notes that are low in frequency and with
little frequency modulation. To produce variation in the song, Audubon’s orioles omit
notes or clips the end of the series (Flood et al., 1990). These characteristics are
unlike most other New World species, especially those formerly incorporated into the
northern oriole species: Baltimore orioles (
Icterus galbula
) and Bullock's orioles (
Icterus bullockii
). These vocal characteristics are similar to those of yellow-backed orioles (
Icterus chrysater
) and bar-winged orioles (
Icterus maculialatus
) (Davis, 1972; Flood et al., 2002).
Audubon’s oriole alarm calls are described by Jaramillo and Burke (1999) as a “nasal
nyyyee”, the amount of time between repetitions decreasing as the bird becomes more
excited.
Food Habits
Audubon’s orioles are primarily insectivorous, consuming beetles (
Coleoptera
), butterflies (
Lepidoptera
), and spiders (
Araneae
). They also eat orchard fruit including plums, peaches, and apples; hackberries;
sunflower seeds; and mesquite beans (
Prosopis
species). They occasionally visit suburban hummingbird and seed feeders (Flood et
al., 2002).
- Primary Diet
- carnivore
- Animal Foods
- insects
- terrestrial non-insect arthropods
- Plant Foods
- seeds, grains, and nuts
- fruit
- nectar
Predation
The nests of Icterus graduacauda are frequently parasitized by bronzed cowbirds ( Molothrus aeneus ) and squirrel cuckoos ( Piaya cayana ) (Jaramillo and Burke, 1999).
Most of the major predators of Audubon’s orioles feed on their eggs or young. These
predators include snakes; ants; birds, including brown jays (
Cyanocorax morio
); and mammals, especially white-nosed coatis (
Nausa naurica
) (Flood, 2002).
Ecosystem Roles
There is little information published regarding ecosystem roles. However, it is speculated
that these orioles help to propagate several species of flowering plants by scattering
their seeds through droppings. In addition, eggs and young are prey to several species
(see predation section). Audobon's orioles may aid in regulating populations of the
insect species that form a large part of their diet.
- Ecosystem Impact
- disperses seeds
- bronzed cowbird ( Molothrus aeneus )
- squirrel cuckoo ( Piaya cayana )
Economic Importance for Humans: Positive
There is little information documenting Audubon’s oriole impact on humans, either positively or negatively. Their potential impact on plant regeneration through seed dispersal may help humans and they may help to regulate some insect populations.
- Positive Impacts
- controls pest population
Economic Importance for Humans: Negative
There are no negative impacts of Audubon’s orioles on humans.
Conservation Status
Audubon’s orioles have experienced a marked decline in population in southern Texas
due to nest parasitism by
bronzed cowbirds
. In addition, the species has been affected by human activities, including the clearing
of habitat for
human
development. It is also suggested that Audubon’s orioles are sensitive to human interference
during the breeding season (Flood et al., 2002).
Other Comments
Audubon’s orioles are similar in coloration to their closest relative,
Icterus chrysater
, commonly known as yellow-backed orioles (Hofmann et al., 2006). In
I. chrysater
and
I. graduacauda
, both sexes have songs of similar complexity (Price et al., 2007). This is typical
of tropical oriole species and has been shown to be the ancestral state of the genus
Icterus
(Hofmann et al., 2008). Analysis of cytrochrome-b and ND-2 genes in genus
Icterus
strongly suggests that the two species are each other’s closest relatives, having
1.7% genetic divergence in the target sequences (Omland et al., 1999). This suggests
that the two clades may have diverged from one another less than one million years
ago, assuming a molecular clock of approximately 2% divergence per million years (Omland
et al., 1999).
Additional Links
Contributors
Tanya Dewey (editor), Animal Diversity Web.
Matthew Murphy (author), University of Maryland, Baltimore County, Kevin Omland (editor, instructor), University of Maryland, Baltimore County.
- Nearctic
-
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- Neotropical
-
living in the southern part of the New World. In other words, Central and South America.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- terrestrial
-
Living on the ground.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- scrub forest
-
scrub forests develop in areas that experience dry seasons.
- suburban
-
living in residential areas on the outskirts of large cities or towns.
- riparian
-
Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).
- endothermic
-
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
- bilateral symmetry
-
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
- monogamous
-
Having one mate at a time.
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- arboreal
-
Referring to an animal that lives in trees; tree-climbing.
- diurnal
-
- active during the day, 2. lasting for one day.
- motile
-
having the capacity to move from one place to another.
- sedentary
-
remains in the same area
- territorial
-
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
- social
-
associates with others of its species; forms social groups.
- visual
-
uses sight to communicate
- acoustic
-
uses sound to communicate
- carnivore
-
an animal that mainly eats meat
- insectivore
-
An animal that eats mainly insects or spiders.
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
References
American Ornithologists' Union, 1998. Check-List of North American Birds . Washington, DC: American Ornithologists' Union.
Bendire, C. 1895. Life histories of North American birds, US National Museum Special Bulletin 3. . Washington, DC: Government Printing Office.
Davis, L. 1972. A field guide to the birds of Mexico and Central America . Austin, TX: University of Texas Press.
Flood, N., J. Rising, T. Brush. 1990. Aspects of the Breeding Biology of Audubon’s Oriole. Journal of Field Ornithology , 61(3): 290-302.
Flood, N., J. Rising, T. Brush. 2002. Audubon's Oriole (Icterus graduacauda). Pp. 1-16 in The Birds of North America , Vol. 691. Philadelphia, PA: The Birds of North America, Inc..
Hofmann, C., T. Cronin, K. Omland. 2008. Carotenoids and melanins contribute to sexual dichromatism in New World orioles. The Auk , in press: in press.
Hofmann, C., T. Cronin, K. Omland. 2006. Using spectral data to reconstruct evolutionary changes in coloration: carotenoid color evolution in New World orioles. Evolution , 60: 1680-1691.
Howell, S., S. Webb. 1995. A Guide to the Birds of Mexico and Northern Central America . New York: Oxford University Press, Inc..
Jaramillo, A., P. Burke. 1999. New World Blackbirds: The Icterids . Princeton, NJ: Princeton University Press.
Omland, K., S. Lanyon, S. Fritz. 1999. A molecular phylogeny of the New World orioles (Icterus): the importance of dense taxon sampling. Molecular Phylogenetics and Evolution , 12: 224-239.
Price, J., N. Friedman, K. Omland. 2007. Song and plumage evolution in the New World orioles (Icterus) show similar lability and convergence in patterns. Evolution , 61: 850-863.
Sibley, D. 2000. The Sibley Guide to Birds . New York: Alfred A. Knopf, Inc..