The Baltimore oriole (Icterus galbula) is a small icterid blackbird common in eastern North America as a migratory breeding bird. It received its name from the resemblance of the male's colors to those on the coat-of-arms of 17th-century Lord Baltimore. Observations of interbreeding between the Baltimore oriole and the western Bullock's oriole Icterus bullockii, led to both being classified as a single species, called the northern oriole, from 1973 to 1995. Research by James Rising, a professor of zoology at the University of Toronto, and others showed that the two birds actually did not interbreed significantly.
The Baltimore oriole is the state bird of Maryland, and the namesake and mascot for the Baltimore Orioles baseball team.
Taxonomy
left|thumb|Baltimore orioles
The Baltimore oriole was formally described in 1758 by the Swedish naturalist Carl Linnaeus in the tenth edition of his Systema Naturae under the binomial name Coracias galbula. He specified the type locality as America, but this was restricted to Virginia in 1931. Linnaeus based his account on the "Baltimore-Bird" that had been described and illustrated by the English naturalist Mark Catesby in his The Natural History of Carolina, Florida and the Bahama Islands that was published between 1729 and 1732. The Baltimore oriole is now one of 32 New World orioles placed in the genus Icterus that was introduced in 1760 by the French ornithologist Mathurin Jacques Brisson. The species is monotypic: no subspecies are recognised.
Like all New World orioles, this species is named after an unrelated, physically similar family found in the Old World: the Oriolidae. The word "Oriole" ultimately derives from the Latin , "golden". The genus name Icterus is from the Ancient Greek , a yellow bird, usually taken to be the Eurasian golden oriole, the sight of which was thought to cure jaundice. The specific galbula is the Latin name for a yellow bird, again usually assumed to be the golden oriole.
Description
This medium-sized passerine measures in length and spans across the wings. Their build is typical of icterids, as they have a sturdy body, a longish tail, fairly long legs and a thick, pointed bill. The body weight averages , with a range of weights from . The male oriole is slightly larger than the female, although the size dimorphism is minimal by icterid standards. Adults always have white bars on the wings.
The adult male is orange on the underparts, shoulder patch, and rump, with some birds appearing a very deep flaming orange and others appearing yellowish orange. All of the rest of the male's plumage is black. The adult female is yellow brown on the upper parts with darker wings, and dull orange yellow on the breast and belly. The juvenile oriole is similar looking to the female, with males taking until the fall of their second year to reach adult plumage.
Distribution and habitat
thumb|Adult female
Baltimore orioles live in the Nearctic in summer, including the Canadian Prairies and eastern Montana in the northwest eastward through southern Ontario, southern Quebec and New Brunswick and south through the eastern United States to central Mississippi and Alabama and northern Georgia. They migrate to winter in the Neotropics as far north as Mexico and sometimes the southern coast of the United States, but predominantly in Central America and northern South America. Some areas of the southern United States may retain orioles all winter if they have feeders that appeal to them. The range of this bird overlaps with that of the similar Bullock's oriole in the Midwest, and the two species were once considered to be conspecific under the name northern oriole because they form fertile hybrids. The Baltimore oriole is a rare vagrant to Western Europe.
left|thumb|Juvenile in Maryland, United States
Baltimore orioles are often found high up in large, leafy deciduous trees, but do not generally reside in deep forests. The species has been found in summer and migration in open woodland, forest edge, and partially wooded wetlands or stands of trees along rivers. They are very adaptable and can breed in a variety of secondary habitats. In recent times, they are often found in orchards, farmland, urban parks and suburban landscapes as long as they retain woodlots. In Mexico, they winter in flowering canopy trees, often over shade coffee plantations.
From 1966 to 2015, the Baltimore oriole experienced a greater than 1.5% annual population decrease throughout the northern and eastern parts of its breeding range. Among other causes Dutch elm disease destroyed a meaningful amount of their favorite nesting locations: elm trees.
Behavior
Song and calls
The Baltimore orioles' song is a short set of recognizable, sweet whistles that sound like "tyew, pyeer, peededoo, and "teer." Calls include "veeer," which is an unusual nasal sound, a low chatter call, and two high calls which sound like "tyew-li and kleek."
The male Baltimore oriole song is a clear whistle with a vibrant tone that flows and includes a brief sequence of notes that are paired and repeated 2-7 times, lasting 1-2 seconds. Sometimes during breeding season mature male orioles will make a "flutter-drum sound" to each other while in flight by making noise as they move their wings. Male orioles sing to proclaim and protect territory. The female Baltimore oriole also sings to communicate and while protecting her nest she gives a distinctive call which sounds like a fierce screech. Both male and female orioles make specific warning calls that sound like inharmonious chatter during combative confrontations. If there are other species of orioles in the area that hear the chatter, they will respond to alert calls and try to help defend the territory.right|thumb|Song of the Baltimore oriole
Breeding
Baltimore orioles are basically solitary outside their mating season. The species is generally considered monogamous, although evidence suggests that extra-pair copulation is relatively common. In the spring, males establish a territory and then display to females by singing and chattering while hopping from perch to perch in front of them. Males also give a bow display, bowing with wings lowered and tail fanned. Depending on their receptiveness, the females may ignore these displays or sing and give calls or a wing-quiver display in response. The wing-quiver display involves leaning forward, often with the tail partly fanned, and fluttering or quivering slightly lowered wings. Trees such as elm, cottonwood, maple, willow, or apple are regularly selected, with the nest usually located around above the ground. The female lays three to seven eggs, with the norm being around four. The eggs are pale gray to bluish-white, measuring on average. The incubation period is 12 to 14 days. Once the nestlings hatch, they are fed by regurgitation by both parents and brooded by the female for two weeks. After this, the young start to fledge, becoming largely independent shortly thereafter. If the eggs, young, or nest are destroyed, the oriole is unable to lay a replacement clutch.
The oldest recorded Baltimore oriole lived to 11 years and 7 months in the wild. They have been recorded living up to 14 years in captivity. They acrobatically clamber, hover, and hang among foliage as they comb high branches. They mainly eat insects, berries, and nectar, and are often seen sipping at hummingbird feeders. Their favored prey is perhaps the forest tent caterpillar moth, which they typically eat in their larval stage, and can be a nuisance species if not naturally regulated by predation. The larvae caterpillar is beaten against a branch until their protective hairs are skinned off before being eaten. They will also consume beetles, grasshoppers, wasps, bugs, and spiders.
Unlike American robins and many other fruit-eating birds, Baltimore orioles seem to prefer only ripe, dark-colored fruit. Orioles seek out the darkest mulberries, the reddest cherries, and the deepest-purple grapes, and will ignore green grapes and yellow cherries even if they are ripe. Baltimore orioles sometimes use their bills to "gape", stabbing their closed bill into soft fruits, then opening them to lap the juice with their tongues. During spring and fall, nectar, fruit, and other sugary foods are readily converted into fat, which supplies energy for migration. Many people now attract Baltimore orioles to their backyards with oriole feeders. Many contain essentially the same food as hummingbird feeders, but are designed for orioles, are orange instead of red, and have larger perches. Baltimore orioles are also fond of halved oranges, grape jelly, and in their winter quarters, the red arils of gumbo-limbo (Bursera simaruba). If they discover a well-kept feeder, orioles lead their young there.
See also
- Orchard oriole
- Scott's oriole
- Audubon's oriole
References
External links
- Baltimore oriole – Cornell Lab of Ornithology
- Baltimore oriole - Icterus galbula – USGS Patuxent Bird Identification InfoCenter
- at bird-stamps.org
- "Field Identification of Female and Immature Bullock's and Baltimore" - Birding 1998, vol. 30 (4): 282-295
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Books
- Rising, J. D., and N. J. Flood 1998. Baltimore Oriole (Icterus galbula). In The Birds of North America, No. 384 (A. Poole and F. Gill, eds.). The Birds of North America, Inc., Philadelphia, PA.
Theses
- Allen ES. Ph.D. (2002). Long-term hybridization and the maintenance of species identity in orioles (Icterus). Indiana University, United States, Indiana.
- Brown BT. Ph.D. (1987). Ecology of riparian breeding birds along the Colorado River in Grand Canyon, Arizona. The University of Arizona, United States, Arizona.
- Butcher GS. Ph.D. (1984). SEXUAL COLOR DIMORPHISM IN ORIOLES (THE GENUS ICTERUS): TESTS OF COMMUNICATION HYPOTHESES (BIRDS, BEHAVIOR, BREEDING BIOLOGY). University of Washington, United States, Washington.
- Irwin RE. Ph.D. (1989). A comparative study of sexual selection on song repertoire size in the avian subfamily Icterinae (Passeriformes:Emberizidae). University of Michigan, United States, Michigan.
- Laudenslayer WFJ. Ph.D. (1981). HABITAT UTILIZATION BY BIRDS OF THREE DESERT RIPARIAN COMMUNITIES. Arizona State University, United States, Arizona.
- Neudorf DL. M.Sc. (1991). Nest defense in four host species of the brown-headed cowbird (Molothrus ater). The University of Manitoba (Canada), Canada.
- Parry D. M.Sc. (1994). The impact of predators and parasitoids on natural and experimentally created populations of forest tent caterpillar, Malacosoma disstria Hubner (Lepidoptera: Lasiocampidae). University of Alberta (Canada), Canada.
- Rising JD. Ph.D. (1968). SYSTEMATIC AND EVOLUTIONARY ASPECTS OF INTERBREEDING BETWEEN THE ORIOLES, ICTERUS GALBULA AND I. BULLOCKII IN NORTH AMERICA. University of Kansas, United States, Kansas.
- Underwood TJ. Ph.D. (2004). Proximate and ultimate influences on egg recognition and rejection behaviour in response to avian brood parasitism. The University of Manitoba (Canada), Canada.
- Williams PL. Ph.D. (1988). Spacing behavior and related features of social organization in Northern Orioles of centraloastal California. University of California, Berkeley, United States, California.
Articles
- Beletsky LD. (1982). Vocal Behavior of the Northern Oriole Icterus-Galbula-Galbula. Wilson Bull. vol 94, no 3. pp. 372–381.
- Biermann GC & Sealy SG. (1985). Seasonal Dynamics of Body Mass of Insectivorous Passerines Breeding on the Forested Dune Ridge Delta-Marsh Manitoba Canada. Canadian Journal of Zoology. vol 63, no 7. pp. 1675–1682.
- Blankespoor HD, Esch GW & Johnson WC. (1985). Some Observations on the Biology of Collyriclum-Faba. Journal of Parasitology. vol 71, no 4. pp. 469–471.
- Bochkov AV & Galloway TD. (2001). Parasitic cheyletoid mites (Acari: Cheyletoidea) associated with passeriform birds (Aves: Passeriformes) in Canada. Canadian Journal of Zoology. vol 79, no 11. pp. 2014–2028.
- Brawn JD. (2006). Effects of restoring oak savannas on bird communities and populations. Conservation Biology. vol 20, no 2. pp. 460–469.
- Brown BT & Trosset MW. (1989). Nesting-Habitat Relationships of Riparian Birds Along the Colorado River in Grand Canyon Arizona USA. Southw Natural. vol 34, no 2. pp. 260–270.
- Browning MR. (1975). FIRST OREGON SPECIMEN OF ICTERUS-GALBULA-GALBULA. Auk. vol 92, no 1. pp. 162–163.
- Butcher GS. (1981). Northern Orioles Icterus-Galbula-Bullockii Disappear with Mount St-Helens Washington USA Ashfall. Murrelet. vol 62, no 1. pp. 15–16.
- Butcher GS. (1984). The Predator-Deflection Hypothesis for Sexual Color Dimorphism a Test on the Northern Oriole Icterus-Galbula-Bullockii. Animal Behaviour. vol 32, no 3. pp. 925–926.
- Butcher GS. (1991). Mate Choice in Female Northern Orioles with a Consideration of the Role of the Black Male Coloration in Female Choice. Condor. vol 93, no 1. pp. 82–88.
- Conover MR. (1982). Behavioral Techniques to Reduce Bird Damage to Blueberries Methiocarb and a Hawk Kite Predator Model. Wildlife Society Bulletin. vol 10, no 3. pp. 211–216.
- Conway WC, Smith LM & Bergan JF. (2002). Avian use of Chinese tallow seeds in coastal Texas. Southw Natural. vol 47, no 4. pp. 550–556.
- Corbin KW & Sibley CG. (1977). Rapid Evolution in Orioles of the Genus Icterus. Condor. vol 79, no 3. pp. 335–342.
- Corbin KW, Sibley CG & Ferguson A. (1979). Genic Changes Associated with the Establishment of Sympatry in Orioles of the Genus Icterus. Evolution. vol 33, no 2. pp. 624–633.
- Davis CA. (2005). Breeding bird communities in riparian forests along the Central Platte River, Nebraska. Great Plains Research. vol 15, no 2. pp. 199–211.
- Davis MA, Peterson DW, Reich PB, Crozier M, Query T, Mitchell E, Huntington J & Bazakas P. (2000). Restoring savanna using fire: Impact on the breeding bird community. Restor Ecol. vol 8, no 1. pp. 30–40.
- Dixon KL. (1989). Contact Zones of Avian Congeners on the Southern Great Plains USA. Condor. vol 91, no 1. pp. 15–22.
- Edinger BB. (1988). Extra-Pair Courtship and Copulation Attempts in Northern Orioles. Condor. vol 90, no 3. pp. 546–554.
- Falardeau G & Desgranges JL. (1991). HABITAT SELECTION AND RECENT FLUCTUATIONS IN POPULATIONS OF FARMLAND BIRDS IN QUEBEC. Can Field-Nat. vol 105, no 4. pp. 469–482.
- Flood NJ. (1984). Adaptive Significance of Delayed Plumage Maturation in Male Northern Orioles Icterus-Galbula. Evolution. vol 38, no 2. pp. 267–279.
- Flood NJ. (1985). INCIDENCES OF POLYGYNY AND EXTRAPAIR COPULATION IN THE NORTHERN ORIOLE. Auk. vol 102, no 2. pp. 410–413.
- Flood NJ. (1990). Aspects of the Breeding Biology of Audubon's Oriole. J Field Ornithol. vol 61, no 3. pp. 290–302.
- Freeman S & Zink RM. (1995). A phylogenetic study of the blackbirds based on variation in mitochondrial DNA restriction sites. Syst Biol. vol 44, no 3. pp. 409–420.
- Graf RL & Greeley F. (1976). NESTING-SITE OF NORTHERN ORIOLE IN AMHERST, MASSACHUSETTS. Wilson Bull. vol 88, no 2. pp. 359–360.
- Greenberg R, Bichier P & Sterling J. (1997). Bird populations in rustic and planted shade coffee plantations of eastern Chiapas, Mexico. Biotropica. vol 29, no 4. pp. 501–514.
- Hobson KA & Sealy SG. (1987). COWBIRD EGG BURIED BY A NORTHERN ORIOLE. J Field Ornithol. vol 58, no 2. pp. 222–224.
- Hubbard GB, Schmidt RE, Eisenbrandt DL, Witt WM & Fletcher KC. (1985). Fungal Infections of Ventriculi in Captive Birds. Journal of Wildlife Diseases. vol 21, no 1. pp. 25–28.
- Jobin B, DesGranges J-L & Boutin C. (1998). Farmland habitat use by breeding birds in Southern Quebec. Canadian Field Naturalist. vol 112, no 4. pp. 611–618.
- Kerlinger P & Doremus C. (1981). Habitat Disturbance and the Decline of Dominant Avian Species in Pine Barrens of the Northeastern USA. American Birds. vol 35, no 1. pp. 16–20.
- Kondo B, Baker JM & Omland KE. (2004). Recent speciation between the Baltimore Oriole and the Black-backed Oriole. Condor. vol 106, no 3. pp. 674–680.
- Labedz TE. (1984). Age and Reproductive Success in Northern Orioles Icterus-Galbula. Wilson Bull. vol 96, no 2. pp. 303–305.
- Lambert C. (1992). Winter northern oriole in Tucker, Dekalb County, Georgia. Oriole. vol 57, no 1-4.
- Mackenzie DI, Sealy SG & Sutherland GD. (1982). Nest Site Characteristics of the Avian Community in the Dune Ridge Forest Delta Marsh Manitoba Canada a Multi Variate Analysis. Canadian Journal of Zoology. vol 60, no 9. pp. 2212–2223.
- Marr NV. (1985). Gopher Snake Pituophis-Melanoleucus Preys on Northern Oriole Icterus-Galbula Nestlings. Murrelet. vol 66, no 3. pp. 95–97.
- Martinez Del Rio C & Eguiarte LE. (1987). Bird Visitation to Agave-Salmiana Comparisons among Hummingbirds and Perching Birds. Condor. vol 89, no 2. pp. 357–363.
- Matson RH. (1989). Distribution of the Testis-Specific Ldh-X among Avian Taxa with Comments on the Evolution of the Ldh Gene Family. Systematic Zoology. vol 38, no 2. pp. 106–115.
- Neudorf DL & Sealy SG. (1992). Reactions of four passerine species to threats of predation and cowbird parasitism: Enemy recognition or generalized responses?. Behaviour. vol 123, no 1-2. pp. 84–105.
- Omland KE, Lanyon SM & Fritz SJ. (1999). A molecular phylogeny of the new world orioles (Icterus): The importance of dense taxon sampling. Mol Phylogenet Evol. vol 12, no 2. pp. 224–239.
- Palmer T. (1992). Population Changes in a Long-Term Northern Oriole Winter Roost in Central Florida. Florida Field Naturalist. vol 20, no 1. pp. 18–20.
- Parry D, Spence JR & Volney WJA. (1997). Responses of natural enemies to experimentally increased populations of the forest tent caterpillar, Malacosoma disstria. Ecol Entomol. vol 22, no 1. pp. 97–108.
- Perkins MW, Johnson RJ & Blankenship EE. (2003). Response of riparian avifauna to percentage and pattern of woody cover in an agricultural landscape. Wildlife Society Bulletin. vol 31, no 3. pp. 642–660.
- Pleasants BY. (1979). Adaptive Significance of the Variable Dispersion Pattern of Breeding Northern Orioles. Condor. vol 81, no 1. pp. 28–34.
- Quay WB. (1989). Timing of Sperm Releases and Inseminations in Resident Emberizids a Comparative Study. Condor. vol 91, no 4. pp. 941–961.
- Quinn JS, Guglich E, Seutin G, Lau R, Marsolais J, Parna L, Boag PT & White BN. (1992). Characterization and Assessment of an Avian Repetitive DNA Sequence as an Icterid Phylogenetic Marker. Genome. vol 35, no 1. pp. 155–162.
- Richardson DS & Bolen GM. (1999). A nesting association between semi-colonial Bullock's orioles and yellow-billed magpies: evidence for the predator protection hypothesis. Behav Ecol Sociobiol. vol 46, no 6. pp. 373–380.
- Richardson DS & Burke T. (1999). Extra-pair paternity in relation to male age in Bullock's orioles. Mol Ecol. vol 8, no 12. pp. 2115–2126.
- Richardson DS & Burke T. (2001). Extrapair paternity and variance in reproductive success related to breeding density in Bullock's orioles. Animal Behaviour. vol 62, pp. 519–525.
- Rising JD. (1973). MORPHOLOGICAL VARIATION AND STATUS OF ORIOLES, ICTERUS-GALBULA, I-BULLOCKII, AND I-ABEILLEI, IN NORTHERN GREAT PLAINS AND IN DURANGO, MEXICO. Can J Zool-Rev Can Zool. vol 51, no 12. pp. 1267–1273.
- Rising JD. (1996). The stability of the oriole hybrid zone in Western Kansas. Condor. vol 98, no 3. pp. 658–663.
- Rohwer S & Johnson MS. (1992). SCHEDULING DIFFERENCES OF MOLT AND MIGRATION FOR BALTIMORE AND BULLOCKS ORIOLES PERSIST IN A COMMON ENVIRONMENT. Condor. vol 94, no 4. pp. 992–994.
- Rosenberg KV, Ohmart RD & Anderson BW. (1982). Community Organization of Riparian Breeding Birds Response to an Annual Resource Peak. Auk. vol 99, no 2. pp. 260–274.
- Roskaft E, Rohwer S & Spaw CD. (1993). COST OF PUNCTURE EJECTION COMPARED WITH COSTS OF REARING COWBIRD CHICKS FOR NORTHERN ORIOLES. Ornis Scandinavica. vol 24, no 1. pp. 28–32.
- Rothstein SI. (1977). COWBIRD PARASITISM AND EGG RECOGNITION OF NORTHERN ORIOLE. Wilson Bull. vol 89, no 1. pp. 21–32.
- Rothstein SI. (1978). Mechanisms of Avian Egg Recognition Additional Evidence for Learned Components. Animal Behaviour. vol 26, no 3. pp. 671–677.
- Schaefer VH. (1980). Geographic Variation in the Insulative Qualities of Nests of the Northern Oriole Icterus-Galbula. Wilson Bull. vol 94, no 4. pp. 466–474.
- Schemske DW. (1975). TERRITORIALITY IN A NECTAR FEEDING NORTHERN ORIOLE IN COSTA-RICA. Auk. vol 92, no 3. pp. 594–595.
- Sealy SG. (1979). Prebasic Molt of the Northern Oriole Icterus-Galbula. Canadian Journal of Zoology. vol 57, no 7. pp. 1473–1478.
- Sealy SG. (1980). Reproductive Responses of Northern Orioles Icterus-Galbula to a Changing Food Supply. Canadian Journal of Zoology. vol 58, no 2. pp. 221–227.
- Sealy SG. (1994). OBSERVED ACTS OF EGG DESTRUCTION, EGG REMOVAL, AND PREDATION ON NESTS OF PASSERINE BIRDS AT DELTA MARSH, MANITOBA. Can Field-Nat. vol 108, no 1. pp. 41–51.
- Sealy SG. (1996). Evolution of host defenses against brood parasitism: Implications of puncture-ejection by a small passerine. Auk. vol 113, no 2. pp. 346–355.
- Sealy SG & Neudorf DL. (1995). Male northern orioles eject cowbird eggs: Implications for the evolution of rejection behaviour. Condor. vol 97, no 2. pp. 369–375.
- Searcy WA & Yasukawa K. (1981). Sexual Size Dimorphism and Survival of Male and Female Blackbirds Icteridae. Auk. vol 98, no 3. pp. 457–465.
- Skowron C & Kern M. (1980). The Insulation in Nests of Selected North American Song Birds. Auk. vol 97, no 4. pp. 816–824.
- Steinegger DH, Aguero DA, Johnson RJ & Eskridge KM. (1991). MONOFILAMENT LINES FAIL TO PROTECT GRAPES FROM BIRD DAMAGE. Hortscience. vol 26, no 7. pp. 924–924.
- Stephen BH, Dawn MB, Ken AE, Michael DC & Lyle F. (2004). Partial cutting of woodlots in an agriculture-dominated landscape: effects on forest bird communities. Canadian Journal of Forest Research. vol 34, no 12. p. 2467.
- Swiderski J. (2002). A winter Baltimore Oriole flock in Valdosta, Georgia. Oriole. vol 67, no 1-2.
- Underwood TJ & Sealy SG. (2006). Grasp-ejection in two small ejecters of cowbird eggs: a test of bill-size constraints and the evolutionary equilibrium hypothesis. Animal Behaviour. vol 71, pp. 409–416.
- Zegers DA, May S & Goodrich LJ. (2000). Identification of nest predators at farm/forest edge and forest interior sites. J Field Ornithol. vol 71, no 2. pp. 207–216.
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