Geographic Range
Bullock’s orioles (
Icterus bullockii
) are native to western North America, especially most of the western United States.
They are common throughout most of their range (Jaramillo and Burke 1999). They are
found as far north as southern British Columbia during the breeding season, (Jaramillo
and Burke 1999; Rising and Williams 1999) but the winter range is largely confined
to Mexico (Jaramillo and Burke 1999; Howell and Webb 1995). Though no geographic boundary
hinders movement to the east, the range generally ends in the western counties of
North Dakota, South Dakota, Kansas, and in central Texas (Jaramillo and Burke 1999;
Rising and Williams 1999). The breeding range extends into southern Canada, including
Vancouver Island, British Columbia, Alberta, and Saskatchewan (Jaramillo and Burke
1999; Rising and Williams 1999). Bullock’s orioles also breed in Durango, Sonora,
and Baja states of northern Mexico (Howell and Webb 1995; Jaramillo and Burke 1999).
Bullock’s orioles are absent from southwestern Arizona and high elevation, arid portions
of Idaho (Rising and Williams 1999).
During winter, Bullock’s orioles may be found throughout Mexico, from Sinaloa south
and east through central Mexico to Oaxaca. They are occasionally seen during the winter
months in Baja California and in Guatemala (Howell and Webb 1995; Jaramillo and Burke
1999; Rising and Williams 1999).
Habitat
Bullock’s orioles prefer riparian corridors, open woodland, and scrub forest (Jaramillo
and Burke 1999). During the breeding season, they are observed in patchy forest dominated
by cottonwood and pecan throughout much of their range (Jaramillo and Burke 1999;
Rising and Williams 1999). Willows (
Salix
) are preferred in riparian areas; by contrast, in arid southwestern Arizona this
species prefers scrub forest trees, especially mesquite (
Prosopis
) and salt cedar (
Tamarix
) (Rising and Williams 1999). During the winter, Bullock’s orioles are often seen
foraging in urban areas, particularly parks. In California, eucalyptus (
Eucalyptus
) is used as a source of nectar (Jaramillo and Burke 1999; Rising and Williams 1999).
- Habitat Regions
- temperate
- tropical
- terrestrial
- Terrestrial Biomes
- savanna or grassland
- forest
- scrub forest
- Other Habitat Features
- suburban
- agricultural
- riparian
Physical Description
Bullock’s orioles are medium-sized orange orioles. This species is sexually dimorphic,
with males being slightly larger than females. Males range in length from 17.2 to
19.3 centimeters, while females are from 16.8 to 19.1 centimeters. Bullock’s orioles
range in mass from 29 to 43 grams (Rising and Williams 1999). The culmen is straight
and mostly black; the lower edge of the culmen is blue (Jaramillo and Burke 1999;
Sibley 2000). In adults of this species, the lower mandible is bluish gray. All exposed
skin is bluish gray (Jaramillo and Burke 1999). In adults, the tail is square and
slightly graduated (Sibley 2000).
During the breeding season, adult males are characterized by their strongly contrasting
black and orange plumage and black throat patch, though older females may also display
a small throat patch. Though the crown is black, the rest of the head is orange, with
a black eye-line that extends to the crown (Jaramillo and Burke 1999; Rising and Williams
1999; Sibley 2000). The supercilium is bright orange. The underparts and breast range
in color from yellow to orange while the back is black (Jaramillo and Burke 1999;
Pyle and Howell 1997; Rising and Williams 1999; Sibley 2000). Although the tail is
mostly black, the outer three or four retrices are tipped orange, forming a dark T
shape beginning at the base of the tail (Jaramillo and Burke 1999; Sibley 2000). The
wing coverts are edged in white, forming a wing panel. The scapulars are black (Jaramillo
and Burke 1999; Rising and Williams 1999).
Adult females are duller and, in most cases, lack the dark throat patch seen in male
Bullock’s orioles (Jaramillo and Burke 1999; Pyle and Howell 1997). The upperparts,
face, and breast are a dull grayish yellow with indistinct dark streaks on the back.
The underparts are grayish, ranging in color from white to yellow (Jaramillo and Burke
1999; Rising and Williams 1999; Sibley 2000). The coverts are fringed white, and do
not form a solid wing-panel as in the male, while the secondaries and tertials are
fringed gray. The crown is olive. Alternatively, adult females may have a small black
throat patch, though they lack the black lores seen in adult males. It is hypothesized
that females with throat patches are older individuals (Jaramillo and Burke 1999).
Immature males resemble adult females, though in adult females the wings show less
abrasion. Immature females are similar to juveniles of both sexes. Immature females
can be distinguished from juveniles by the presence of worn, dark-tipped outer coverts,
fresh white-tipped inner coverts, and brown medial coverts that are tipped white.
Juveniles cannot be sexed in the field through differences in plumage. In general,
juveniles resemble adult females, but with darker wings, less-extensive wing bars,
the lack of a malar (throat) patch, and the presence of a pink mandible (Jaramillo
and Burke 1999).
- Other Physical Features
- endothermic
- homoiothermic
- bilateral symmetry
- Sexual Dimorphism
- male larger
- sexes colored or patterned differently
- male more colorful
Reproduction
Bullock’s orioles are seasonally monogamous, forming pair bonds that last for a single
breeding season (Rising and Williams 1999).
- Mating System
- monogamous
Males arrive at the breeding ground approximately two weeks before females. Breeding
begins in May and continues until mid July. The breeding season varies geographically
and tends to begin and end later in the west and in northern latitudes (Jaramillo
and Burke 1999; Harrison 1978; Rising and Williams 1999).
Bullock’s oriole nests are deep, pensile structures and are usually suspended on the
outer branches of a tree (Harrison 1978). Nests are on average 6 inches (15 cm) deep
and 4 inches (10 cm) in diameter, the walls of which are approximately 0.75 inches
(1.9 cm) thick (Bent 1958). The nest opening is contracted and oval-shaped (Bent 1958).
The nest is constructed primarily of plant fiber, especially flax fiber, oat stalks,
and the interior bark of willow and juniper trees; horsehair and twine are also used
when the nest is built near human developments. The nest is lined with plant down,
wool, hair, and moss (Bent 1958; Harrison 1978). Both male and female have been observed
to participate in nest construction, though normally only the female weaves the nest
(Bent 1958). Nests are abandoned at the end of the breeding season and are not reused
(Sibley 2000).
Eggs are laid in clutches of 3 to 6, with clutches of 4 or 5 eggs being the most common
(Harrison 1978; Sibley 2000). The eggs themselves are small, approximately 2.5 cm
long by 1.5 cm in diameter. Nest size is variable, and according to Schaefer (1976),
nests range in depth from 10 cm to 38 cm. Eggs are whitish with dark purple or brown
scrawling patterns near the wide end of the egg (Harrison 1978).
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
Only the female incubates the eggs, which hatch after approximately two weeks (Harrison
1978). Nestlings are altricial: they are entirely reliant on parental care for their
survival (Sibley 2000). Both sexes care for the young, providing them with food as
well as defending the nest from predators (Bent 1958).
- Parental Investment
- altricial
-
pre-fertilization
- provisioning
-
protecting
- female
-
pre-hatching/birth
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
Lifespan/Longevity
The current observed maximum lifespan in the wild is 7 years, most individuals do
not survive this long (USGS: Patuxent Wildlife Research Center).
Behavior
Bullock’s orioles are most often seen in pairs during the breeding season, occasionally
forming small flocks. They are territorial during the breeding season, males aggressively
defending nesting sites (Rising and Williams 1999). Although the nest is defended
from conspecifics, mutual feeding grounds are usually unguarded. Although territoriality
has not been extensively studied during the winter months, Bullock’s orioles will
defend flowering
Erythrina breviflora
, a source of nectar, from other species, particularly hummingbirds (
Trochilidae
) (Jaramillo and Burke 1999; Rising and Williams 1999). While breeding pairs nest
singly, nests tend to be clustered. Breeding density tends to be highest in areas
where there food is most abundant. Bullock’s orioles migrate at night, forming small
flocks of up to ten individuals (Rising and Williams 1999).
Home Range
A family of
Icterus bullockii
living in Kansas was observed to have a home range of 0.85 hectares (Fitch 1958;
Zeiner et al. 1988).
Communication and Perception
Vocalization forms the primary method of communication for Bullock’s orioles. Vocal
communications include two short, energetic songs described by Dawson (1923) as kip,
kit-tick, kit-tick, whew, wheet and cut cut cudut whee up chooup; the latter sequence
is less common than the former. In the latter sequence, the last note is often unclear
(Bent 1958).
Both males and females sing, female song being lower in pitch and less sweet than
that of the male. Females are most likely to sing earlier in the season, and have
been observed to sing while constructing the nest. Males sometimes give a short cry
while with their mate (Bent 1958).
Baltimore
and Bullock’s orioles have similar songs, though
Baltimore orioles
tend to have harsher songs than Bullock’s orioles (Bent 1958; Wheelock 1903).
Food Habits
Bullock’s orioles are primarily insectivorous. During the breeding season, they feed
mostly on butterflies and their larvae (
Lepidoptera
) and augment their diet with beetles (
Coleoptera
), weevils (
Curculionoidea
), and scale insects (
Coccoidea
). Bullock’s orioles occasionally eat mollusks and small lizards. In one case, a member
of this species was observed killing and eating a hummingbird. Fruit is also a major
food source, accounting for approximately 40% of this species diet during the summer
months (Sibley 2001). Stomach content analyses indicate that Bullock’s orioles especially
favor cherries, blackberries, raspberries, and figs (Bent 1958).
Bullock’s orioles either glean insects from leaves or forage in clearings. One behavior,
common to the
icterids
, is called gaping: the bill is inserted into soil or a plant stem and then forced
open. This behavior leaves an opening that may uncover prey species (Sibley 2001).
- Primary Diet
- carnivore
- Animal Foods
- birds
- insects
- Plant Foods
- seeds, grains, and nuts
- fruit
- nectar
Predation
Predators include jays, magpies, crows, and squirrels (Bent 1958; Jaramillo and Burke
1999). All four feed on the eggs or young of Bullock’s orioles. Nests are sometimes
parasitized by cowbirds; however, Bullock’s orioles seem to be better able to identify
parasitic eggs. They remove cowbird eggs by puncturing the shell with the bill and
removing the egg from the nest, though an individual removing cowbird eggs in this
manner risks damaging its own eggs (Bent 1958).
Ecosystem Roles
Bullock’s orioles help to spread the seeds of several plant species. Their eggs and young are a food source for several species and help keep insect populations in check. Please see the previous sections for more detailed information, especially “Food Habits” and “Predation”.
- Ecosystem Impact
- disperses seeds
Economic Importance for Humans: Positive
Bullock’s orioles regulate the populations of black olive scale insects (
Parlatoria oleae
), which in large numbers have the potential to destroy olive crops. Bullock’s orioles
also consume cotton boll weevils (
Anthonomus grandis
), insects that can negatively impact cotton production (Bent 1958; Howell 1907).
Bullock’s orioles are not known to have any significant negative impact on crop production.
- Positive Impacts
- research and education
- controls pest population
Economic Importance for Humans: Negative
Bullock's orioles do not have any significant negative economic impact.
Conservation Status
Bullock’s orioles have declined in population size in North America since the 1960s,
though this species is not considered endangered (Sibley 2001). Human factors contribute
to this decline, through habitat degradation and the use of insecticides. An increase
in habitat availability, caused by the planting of shelterbelts and by human control
of brush fires, has probably led to population stability in the Great Plains. However,
irrigation has reduced available water supplies in some parts of Kansas and Colorado,
which likely negatively affects the carrying capacity for Bullock’s orioles in these
regions.
Unlike most migratory, riparian species, Bullock’s orioles have not seen a population
decline in the Colorado River Valley (Rising and Williams 1999)
Additional Links
Contributors
Matthew Murphy (author), University of Maryland, Baltimore County, Kevin Omland (editor, instructor), University of Maryland, Baltimore County, Tanya Dewey (editor), Animal Diversity Web.
- 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.
- temperate
-
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
- 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.
- tropical savanna and grassland
-
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
- savanna
-
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
- temperate grassland
-
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
- 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.
- agricultural
-
living in landscapes dominated by human agriculture.
- 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.
- altricial
-
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
- 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.
- migratory
-
makes seasonal movements between breeding and wintering grounds
- 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
Bent, A. 1958. Life histories of North American Blackbirds, Orioles, Tanagers, and Allies . New York, New York: Dover Publications, Inc..
Davis, L. 1972. A Field guide to the birds of Mexico and Central America . Austin, TX: University of Texas Press.
Dawson, W. 1923. The Birds of California . San Diego, CA: South Moulton Co..
Fitch, H. 1958. Home ranges, territories, and seasonal movements of vertebrates of the Natural History Reservation. Publ. Mus. Nat. Hist. , 11: 63-326.
Harrison, C. 1978. A Field Guide to the Nests, Eggs and Nestlings of North American Birds . Glasgow, Scotland: William Collins Sons & Co. Ltd..
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.
Klimkiewicz, M., A. Futcher. 1987. Longevity records of North American birds: Coerbinae through Estrildidae. Journal of Field Ornithology , 58: 318-333.
Pyle, P., S. Howell. 1997. Identification Guide to North American Birds: Columbidae to Ploceidae . Bolinas, CA: Slate Creek Press.
Rising, J., P. Williams. 1999. Bullock's Oriole. Pp. 1-20 in The Birds of North America , Vol. 416. Philadelphia, PA: The Birds of North America, Inc..
Sibley, D. 2001. The Sibley Guide to Bird Life & Behavior . New York: Random House, Inc..
Sibley, D. 2000. The Sibley Guide to Birds . New York: Alfred A. Knopf, Inc..
Wheelock, I. 1903. Birds of Californiaa . Chicago, IL: A. C. McClurg and Co..
Zeiner, D., W. Laudenslayer Jr.. 2009. "California's Wildlife, Vol. I-III" (On-line pdf). CWHR Life History and Range Maps. Accessed December 23, 2009 at http://www.dfg.ca.gov/biogeodata/cwhr/cawildlife.aspx .
US Department of Agriculture. The relation of birds to the cotton boll weevil. 29. Washington, DC: US Dep. Agric. Biol. Surv. Bulletin. 1907.