dcsimg

Lifespan, longevity, and ageing

provided by AnAge articles
Maximum longevity: 14 years
license
cc-by-3.0
copyright
Joao Pedro de Magalhaes
editor
de Magalhaes, J. P.
partner site
AnAge articles

Trophic Strategy

provided by Animal Diversity Web

Baltimore orioles eat primarily caterpillars, including many pest species. They also eat other insects, some small fruits, and nectar. They are an important predator of the nuisance forest tent caterpillar, Malacosoma disstria, which it eats in both its larval and pupal forms. Large larvae are seized and smashed against a twig to break them open and avoid the setae (stiff, hair-like structures). Pupae are pulled out of their cocoon.

In suburban and rural areas, I. glabula can be attracted to feeders by providing orange halves, grape jelly, or artificial nectar. Adults who come to feeders will take their young to the feeder once they are fledged.

Baltimore orioles eat primarily caterpillars, including many pest species. They also eat other insects, some small fruits, and nectar. They are an important predator of the nuisance forest tent caterpillar, which it eats in both its larval and pupal forms. Large larvae are seized and smashed against a twig to break them open and avoid the setae (stiff, hair-like structures). Pupae are pulled out of their cocoon.

In suburban and rural areas, Baltimore orioles can be attracted to feeders by providing orange halves, grape jelly, or artificial nectar. Adults who come to feeders will take their young to the feeder once they are fledged.

Animal Foods: insects; terrestrial non-insect arthropods; mollusks

Plant Foods: fruit; nectar

Primary Diet: carnivore (Insectivore )

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Associations

provided by Animal Diversity Web

Baltimore orioles have many different kinds of predators, including larger birds and mammals. Most predators take eggs, nestlings, or fledglings. In western Massachusetts, avain predators caused 16% of egg losses and 9% of nestling and fledgling losses. In response to predators, both males and females give alarm calls, and chase and mob (harass) predators.

Known Predators:

  • common grackles (Quiscalus quiscula)
  • American crows (Corvus brachyrhynchos)
  • eastern screech owls (Otus asio)
  • blue jays (Cyanocitta cristata)
  • black-billed magpies (Pica pica)
  • red squirrels (Tamiasciurus hudsonicus)
  • fox squirrels (Sciurus niger)
  • eastern gray squirrels (Sciurus carolinensis)
  • domestic cats (Felis silvestris)
license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Morphology

provided by Animal Diversity Web

Adult birds are 17 to 20 cm long, somewhat smaller than a robin. There is sexual dimorphism in plumage and in size; males are 1-5% larger than females in a variety of measurements. Adult males have a black head, bill, and back, and a bright orange breast, rump, and underparts. Their wings are black with orange and white wing bars, and the tail is orange with black streaks. Adult females are paler than males, olive-brown to orange. Their wings are brown with white wing bars, and the bill is gray. She may have traces of black on her head. Immature animals are variable, but typically resemble the female. Males take over a year to reach adult plumage.

Range mass: 28 to 42 g.

Range length: 17 to 20 cm.

Range wingspan: 9 to 10 cm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger; sexes colored or patterned differently; male more colorful

Average basal metabolic rate: 0.5052 W.

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Life Expectancy

provided by Animal Diversity Web

The oldest recorded Baltimore oriole in the wild lived to 11 years and 7 months old. They have been recorded living 14 years in captivity.

Range lifespan
Status: wild:
11.5 (high) years.

Range lifespan
Status: captivity:
14 (high) years.

Average lifespan
Status: wild:
139 months.

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Habitat

provided by Animal Diversity Web

Baltimore orioles prefer open woods, with a strong preference for deciduous over coniferous trees. They are very adaptable, however, and can be found breeding in a variety of habitats. They are rare on farmlands but have adapted well to urban parks and suburban landscapes. In Mexico, they winter in flowering canopy trees over shade coffee plantations.

Habitat Regions: temperate ; tropical ; terrestrial

Terrestrial Biomes: savanna or grassland ; forest ; rainforest ; scrub forest

Other Habitat Features: urban ; suburban ; agricultural ; riparian

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Distribution

provided by Animal Diversity Web

Baltimore orioles are neotropical migrants. They spend summers in the Nearctic, primarily the eastern United States. They breed from Wisconsin to Maine and south to central Mississippi and Alabama, northern Georgia, and western South Carolina and North Carolina. They winter in the neotropics as far north as Mexico and sometimes the southern coast of the United States.

Biogeographic Regions: nearctic (Native ); neotropical (Native )

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Associations

provided by Animal Diversity Web

Baltimore orioles are important predators on insects in the communities in which they live. Because they live in forested areas and prey on caterpillars, the lifestage at which many insects do most damage to plants, they are especially important in protecting forest trees from damage.

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Benefits

provided by Animal Diversity Web

Baltimore orioles are attractive songbirds that will come to feeders. They are generally liked by both serious birdwatchers and casual backyard enthusiasts for both their appearance and song. They are also important predators on some insect pests such as forest tent caterpillars.

Positive Impacts: ecotourism ; controls pest population

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Benefits

provided by Animal Diversity Web

Baltimore orioles may occasionally damage crops of peas or small fruits.

Negative Impacts: crop pest

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Conservation Status

provided by Animal Diversity Web

Baltimore orioles are protected by the Migratory Bird Treaty Act. They may be at risk due to habitat loss, as they prefer wooded areas, but this is not well documented. Although direct human impacts on oriole populations are unknown, the increase in number of orioles wintering in temperate North America may be due to an increase in bird feeders in backyards and elsewhere.

US Migratory Bird Act: protected

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Behavior

provided by Animal Diversity Web

The male sings all summer. His song is rich and flute-like, with each individual having a distinct song. The female song is generally shorter and simpler. The call, from both sexes, is a whistled "hew-li." Nestlings beg loudly.

Baltimore orioles also use postures and movements to communicate, such as male courtship displays, female wing-flutter displays, and nestling wing-flutters when begging for food.

Communication Channels: visual ; acoustic

Perception Channels: visual ; tactile ; acoustic ; chemical

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Untitled

provided by Animal Diversity Web

Baltimore orioles were previously considered a supspecies of northern orioles (Icterus galbula galbula) along with Bullock's orioles (Icterus glabula bullockii), a western North American oriole. They are currently considered separate species: Baltimore orioles, Icterus galbula, and Bullock's orioles, Icterus bullockii. Some hybridization occurs in the Great Plains where these species overlap.

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Reproduction

provided by Animal Diversity Web

Baltimore orioles are generally considered monogamous, although evidence suggests that extra-pair copulation is reasonably common. In the spring, males display to females on their territory by singing and/or chattering while hopping from perch to perch in front of her. Males give a bow display, bowing with wings lowered and tail fanned. Some females ignore these displays while others sing and give calls or a wing-quiver display in response. The wing-quiver display involves leaning forward, often with tail partly fanned, and fluttering or quivering slightly lowered wings.

Mating System: monogamous ; polygynandrous (promiscuous)

Males arrive on breeding grounds in the spring a few days before females. Courtship displays by the male consist of bowing, to show off the bright orange front and black back, and singing. The female builds a woven pouch nest hanging from the end branches of trees, well concealed by leaves. She builds a new nest each year with little or no help from the male. Icterus galbula prefers to build in elms, maples, willow, or apples, twenty-five to thirty feet above the ground. Any available plant and animal fibers may be used.

The female lays four to six eggs, typically four. The eggs are pale grayish or bluish white, irregularly blotched and streaked with browns and black. The female incubates for twelve to fourteen days. Both parents feed the nestlings. Fledglings will stay with their parents for two weeks, and are fed by their parents duing that period. Baltimore orioles lay only one brood per season.

Breeding interval: Baltimore orioles breed once yearly.

Breeding season: Breeding occurs from May to June.

Range eggs per season: 3 to 7.

Average eggs per season: 4.

Range time to hatching: 11 to 14 days.

Average time to hatching: 12 days.

Average time to independence: 2 weeks.

Average age at sexual or reproductive maturity (female): 1 years.

Average age at sexual or reproductive maturity (male): 1 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; oviparous

Average eggs per season: 4.

The female alone broods nestlings; the male occasionally feeds the brooding female, but she usually forages for herself. Parents feed nestlings by regurgitation during the first few days of the nesting period.

Parental Investment: no parental involvement; altricial ; pre-fertilization (Protecting: Female); pre-hatching/birth (Protecting: Female); pre-weaning/fledging (Provisioning: Male, Female, Protecting: Male, Female); pre-independence (Provisioning: Male, Female, Protecting: Male, Female)

license
cc-by-nc-sa-3.0
copyright
The Regents of the University of Michigan and its licensors
bibliographic citation
Kennedy, S. 2001. "Icterus galbula" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Icterus_galbula.html
author
Sara Kennedy, University of Michigan-Ann Arbor
editor
Terry Root, University of Michigan-Ann Arbor
editor
Kathleen Bachynski, University of Michigan-Ann Arbor
editor
Tanya Dewey, Animal Diversity Web
original
visit source
partner site
Animal Diversity Web

Brief Summary

provided by EOL authors
The bright orange and black Baltimore Oriole (Icterus galbula) was named in reference to the colors of the coat of arms of the 17th century Lord Baltimore. These orioles are widespread in North America east of the Great Plains during the northern summer and winter mainly from Mexico south to northern Colombia, northern Venezuela, and Trinidad, although small numbers may winter in the southeastern United States and Greater Antilles. As a result of frequent hybridization between the Bullock's (I. bullockii) and Baltimore Orioles where their ranges meet in the Great Plains, these two orioles were at one time treated as conspecific (i.e., members of the same species), representing two forms of a species that was known as the Northern Oriole. However, genetic studies have indicated that these two species are not even each other’s closest relatives (for a full discussion of this issue, see Jacobsen and Omland 2011). Baltimore Orioles breed in deciduous and mixed woodlands, usually in open woods or along edges rather than in the interior of dense forests. They may be common in towns and other relatively developed areas with appropriate trees (especially elms). The familiar nest of the Baltimore Oriole is a hanging pouch woven of plant fibers and may be seen in shade trees in towns and suburbs. The nest is typically attached firmly by its rim near the end of a slender drooping branch 6 to 9 (sometimes 2 to 18 or more) meters above the ground. There are 4 to 5 eggs (range 3 to 6) eggs. Eggs are incubated by the female for around 12 to 14 days. Nestlings are fed by both parents and leave the nest around 12 to 14 days after hatching.The diet include mainly insects in summer, especially caterpillars, including hairy types avoided by many other birds. They also consume many berries and sometimes cultivated fruit. They may feed on nectar from some flowers and will take sugar water at feeders. The liquid, musical tones of the Baltimore Oriole's song floating down from the treetops are a familiar harbinger of spring in the eastern United States. (Kaufman 1996; AOU 1998)
license
cc-by-3.0
original
visit source
partner site
EOL authors

Comprehensive Description

provided by Smithsonian Contributions to Zoology
Icterus galbula (Linnaeus)

Experiments involving the addition of foreign eggs to nests that contained 2 or more oriole eggs demonstrated that this oriole is a rejecter species. Artificial cowbird eggs were rejected at 18 nests. Real cowbird or house sparrow eggs (which are similar to cowbird eggs) were rejected at another 5 nests. The experiments, involving many species, indicate that while ejection is the normal type of rejection, this oriole is distinctive in that it ejects by spiking cowbird eggs. Other rejecters eject by lifting the eggs in their bills. These experiments were done in California, Manitoba, Ontario, and Connecticut and thus tested both the Bullock's and Baltimore forms of this species (Rothstein, in press (c)). Additional evidence of rejection was sent to us by R. Robertson and R. Norman, who placed real cowbird eggs in 5 nests at Delta, Manitoba. Each cowbird egg was ejected.

The least demanding explanation for the origin of rejection behavior is that it evolved in response to brood parasitism and that it decreases the deleterious effects of the parasitism. This interpretation will be supported if it can be shown that cowbird parasitism, if accepted, reduces the oriole's reproductive output. Reproductive loss due to allowing a cowbird egg to hatch is too poorly known to be measured accurately, but that it occurs is indicated in the case of every nest we know of in which a cowbird egg hatched. One cowbird, but no orioles, fledged from a nest reported by Nauman (1930). Gregg (in Friedmann 1963:133) noted a nest containing a cowbird “big enough to fly” and 2 orioles much less advanced in development. Tate (in Friedmann, 1963:133) found 2 dead oriole nestlings below a nest that contained 1 oriole and 2 cowbirds. M. R. White (unpublished 1945 MS in files of the University of Michigan Biological Station) described a nest in which a cowbird hatched 1 to 2 days before 4 orioles hatched. One of the orioles died before it was 4 days old and the cowbird was so advanced in development that it fledged when the remaining orioles were only 6 to 7 days old. (Orioles fledge after 11 to 14 days; Bent, 1958.) Each nest demonstrates either the death of some oriole young or such a great disparity in size between cowbird and oriole nestlings that the viability of the latter was almost certainly reduced. Also, Newman (1969) reported a fledged cowbird being fed by a female oriole that appeared to have no young of her own. Thus, the rejection behavior elucidated by the experiments has adaptive value that is potentially very high, although knowledge of the actual rate of parasitism of the oriole is needed before the adaptive value can be quantified (Rothstein, 1975b).

Only a small number of additional records of natural parasitism have come to light in recent years but the oriole's rejecter status makes the paucity of records more understandable. In New York, Bull (1974:537) reported 6 instances of parasitism, 5 of which are additional to the 1963 compilation (Friedmann, pp. 132–133). T. S. Smith (1972) observed the ejection of a naturally deposited cowbird egg. This occurred in Nebraska and involved the eastern race of the cowbird, M. ater ater. The records reported by White and Newman (above paragraph) which occurred near Pellston, Michigan, and in Johnston County, Oklahoma, respectively, also refer to M. a. ater. Eight cases of parasitism by this race were reported from Ontario (Peck 1975). (Possibly some of these Ontario cases are referable to M. ater artemisiae since this race replaces M. a. ater in extreme western Ontario.) The Western Foundation has 2 sets parasitized by M. a. ater, 1 from Pennsylvania, the other from Ontario. There are 4 new records for the northwestern race of the parasite, M. ater artemisiae. One, published by Nero (1971), was the first record for Manitoba. A second Manitoba case was found by R. S. Miller in 1972 at Delta, Manitoba. The third case, now in the Delaware Museum of Natural History, was collected at Belvedere, Alberta. The fourth case, from Minnesota, is at the Western Foundation.

Except for Newman's (1969) record which may have involved a hybrid, all the above records of parasitism refer to the eastern (Baltimore) form of this oriole. There are 5 new records for the western (Bullock's) form. The Santa Barbara Museum of Natural History has a set of 4 oriole eggs and 1 cowbird egg taken at Vernon, Texas, 31 May 1966, and one of us (S.I.R.) found 3 cases of parasitism (described below) near Shandon, San Luis Obispo County, California. The Western Foundation has a parasitized set from El Centro, Imperial County, California. The Texas record is referable to M. ater ater, the 4 California records to M. ater obscurus.

While isolated reports of parasitism of the oriole are important, data on the incidence of parasitism in large series of nests have greater value. The Western Foundation has 283 sets of eggs, only 4 of which (1.4 percent) contain cowbird eggs. The 8 Ontario records reported by Peck (1975) make up 2.5 percent of the total sample of 318 nests in the Ontario Nest Record Scheme. The 3 records from Shandon, California, make up 8.8 percent of the 34 nests S.I.R. found in that area in 1974 and 1975. Of course, even these data do not accurately reflect the proportion of northern oriole nests actually parasitized because orioles may remove most cowbird eggs before the eggs are seen.

Techniques to estimate the amount of parasitism of rejecter species that goes unseen are discussed elsewhere (Rothstein, in press (b)). Two additional techniques that are especially applicable to this oriole are as follows. (1) Although these orioles usually drop ejected cowbird eggs at least several meters from their nest (Rothstein, in press (c)), some apparently drop them directly from the nest (see Friedmann, 1963:132–133; Smith, 1972). Inspection of the ground beneath oriole nests might reveal some of the cowbird eggs ejected before the inspection of the nest by an observer. Parasitism at 1 of the Shandon nests was detected in this manner when pieces of cowbird eggshell were found directly beneath an oriole nest that was not close to any other nests. (2) Experiments on the ontogeny of the northern oriole's egg recognition (S.I.R., in prep.) showed a small proportion of orioles learn to accept artificial cowbird eggs added to nests before the onset of laying. Orioles breeding for the first time apparently imprint on the first eggs that appear in their nest. The remaining orioles reject artificial cowbird eggs added before the onset of laying but most of them do not succeed in ejecting the artificial (plaster) egg because they cannot spike it. They peck at it and damage it but after several days some (perhaps all) habituate to the egg and cease their rejection attempts. The end result, whether the orioles initially accept the artificial egg or first try to eject it and then habituate, is that rejection behavior is “turned off” during part or all of the laying stage, if an artificial cowbird egg is added before laying begins. Thus, a sample of birds subjected to this experiment should reveal much of the natural parasitism that occurs, although some parasitism might still be missed if cowbirds lay before orioles have habituated and if the appearance of a naturally deposited cowbird egg is very different from that of the artificial egg to which the orioles imprinted or habituated. The presence of the artificial cowbird egg in such nests should not alter the likelihood of natural parasitism because the presence of a cowbird egg has little or no effect on the probability that a nest will receive additional cowbird eggs (Mayfield, 1965).

One nest in the ontogeny experiments at which orioles accepted the artificial cowbird egg was naturally parasitized as was another nest at which the orioles habituated to the artificial cowbird egg (nests 75–96 and 75–116, respectively). The cowbird eggs in these nests were laid between 22 and 28 May 1975. Both were accepted since they were still present and undamaged on 5 June. The cowbird egg was missing from nest 75–116 on 12 June but as the nest then contained 1 dead plus 1 live oriole nestling and an addled oriole egg, the cowbird could have hatched, then died and been removed. The cowbird egg in nest 75–96 did not hatch. It and 2 dead oriole nestlings were in the nest on 17 June.

Thus, the 3 cases of parasitism near Shandon would probably not have been detected had not special techniques been applied (checking the ground beneath nests, imprinting and habituating orioles to cowbird eggs). These special techniques were not applied at most of the other 34 nests studied near Shandon so the incidence of parasitism could have been higher than 3 of 34 (8.8 percent), since much natural parasitism would still have gone undetected. It is important to point out that cowbirds are uncommon near Shandon so the relatively high figure (8.8 percent) for the minimum incidence of parasitism was not due to an unusually large number of cowbirds. Rather, it was most likely due to the fact that the special techniques applied made it possible to detect parasitism that normally goes unseen. Application of these techniques in other areas where cowbirds are more common might reveal much higher incidences of parasitism. As with the cedar waxwing (discussed previously) these data on cowbird parasitism near Shandon imply that cowbirds not infrequently parasitize rejecter species even though their chances for reproductive success are virtually nil.

RUSTY BLACKBIRD
license
cc-by-nc-sa-3.0
bibliographic citation
Friedmann, Herbert, Kiff, Lloyd F., and Rothstein, Stephen I. 1977. "A further contribution of knowledge of the host relations of the parasitic cowbirds." Smithsonian Contributions to Zoology. 1-75. https://doi.org/10.5479/si.00810282.235

Baltimore oriole

provided by wikipedia EN

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.[2]

The Baltimore oriole is the state bird of Maryland. It is also the namesake and mascot for the Baltimore Orioles baseball team.

Taxonomy

The Baltimore oriole was one of the many bird species originally described by Carl Linnaeus in the 1758 10th edition of his Systema Naturae, where it was given the binomial name of Coracias galbula.[3]

Like all New World orioles, this species is named after an unrelated, physically similar family found in the Old World: the Oriolidae. "Oriole" ultimately derives from Latin aureolus, "golden".[4] The genus name Icterus is from Ancient Greek ikteros, 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.[5]

Description

This medium-sized passerine measures 17–22 cm (6.7–8.7 in) in length and spans 23–32 cm (9.1–12.6 in) 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 33.8 g (1.19 oz), with a range of weights from 22.3 to 42 g (0.79 to 1.48 oz).[6] The male oriole is slightly larger than the female, although the size dimorphism is minimal by icterid standards.[7][8][9] 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.

Some adult males (left) may lack the vivid orange coloration associated with the species, causing them to strongly resemble the yellow Scott's oriole (center) or similar Audubon's oriole (right)

Distribution and habitat

Adult female

Baltimore orioles are found 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.

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.[10]

From 1966–2015, the Baltimore oriole experienced a greater than 1.5% annual population decrease throughout the northern and eastern parts of its breeding range.[11] Among other causes Dutch elm disease destroyed a meaningful amount of their favorite nesting locations: elm trees.[12]

Behavior

Song and calls

The male sings a loud flutey whistle, with a buzzy, bold quality, a familiar sound in much of the eastern United States. The male typically sings from the tree canopy, often giving away its location before being sighted.

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 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 tail partly fanned, and fluttering or quivering slightly lowered wings.

The Baltimore oriole's nest is built by the female. It is a tightly woven, bindle-like pouch located on the end of a branch, consisting of any fine plant or animal materials available, hanging down on the underside.[13] Trees such as elm, cottonwood, maple, willow, or apple are regularly selected, with the nest usually located around 7 to 9 m (23 to 30 ft) 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 2.3 cm × 1.6 cm (0.91 in × 0.63 in) 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.[10]

Mortality

Predation of adults is a common source of mortality, typically also occurring with eggs, nestlings and fledglings. Common predators at Baltimore oriole nests can include common grackles, American crows, blue jays, black-billed magpies, tree squirrels and domestic cats, which most commonly capture newly fledged orioles or adults engaged in brooding behavior. Rapacious birds commonly prey on both young and fully-grown orioles, the most prolific being the eastern screech owl and Cooper's and sharp-shinned hawks. Somewhat larger rapacious birds also sometimes opportunistically prey on the oriole, including peregrine falcons, great horned owls, and barn owls, while merlins may do so while orioles are migrating.[14][15]

The record lifespan for a wild bird was 12 years and 0 months (based on a banded bird killed by a peregrine falcon), with captive orioles living up to 14 years.

Feeding

Adult male Baltimore oriole at grape jelly feeder
Orange and black bird with its beak in an orange
Adult male gaping

Baltimore orioles forage in trees and shrubs, also making short flights to catch insects. 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 are beaten against a branch until their protective hairs are skinned off before being eaten. They will also consume beetles, grasshoppers, wasps, bugs, and spiders.[12] 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 it 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, and 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).[16] If they discover a well-kept feeder, orioles lead their young there.

See also

References

  1. ^ BirdLife International (2018). "Icterus galbula". IUCN Red List of Threatened Species. 2018: e.T22724126A132026652. doi:10.2305/IUCN.UK.2018-2.RLTS.T22724126A132026652.en. Retrieved 12 November 2021.
  2. ^ Reid, Bruce (March 7, 1995). "Oriole Name Migrates to Baltimore". Baltimore Sun. Archived from the original on May 24, 2015.
  3. ^ Linnaeus, Carl (1758). Systema Naturae per Regna Tria Naturae, Secundum Classes, Ordines, Genera, Species, cum Characteribus, Differentiis, Synonymis, Locis. Tomus I. Editio decima, reformata (in Latin). Holmiae (Stockholm, Sweden): Laurentius Salvius. p. 108.
  4. ^ "Oriole". Oxford English Dictionary (Online ed.). Oxford University Press. (Subscription or participating institution membership required.)
  5. ^ Jobling, James A. (2010). The Helm Dictionary of Scientific Bird Names. London, United Kingdom: Christopher Helm. pp. 168, 201. ISBN 978-1-4081-2501-4.
  6. ^ CRC Handbook of Avian Body Masses by John B. Dunning Jr. (Editor). CRC Press (1992), ISBN 978-0-8493-4258-5.
  7. ^ Baltimore Oriole, Life History, All About Birds – Cornell Lab of Ornithology. Allaboutbirds.org. Retrieved on 2012-08-23.
  8. ^ ADW: Icterus galbula: INFORMATION. Animaldiversity.ummz.umich.edu. Retrieved on 2012-08-23.
  9. ^ Baltimore Orioles, Baltimore Oriole Pictures, Baltimore Oriole Facts – National Geographic. Animals.nationalgeographic.com. Retrieved on 2012-08-23.
  10. ^ a b Rising, J., N. Flood. 1998. Baltimore Oriole: The Birds of North America, No. 384: 1–32.
  11. ^ "Baltimore Oriole Icterus galbula BBS Trend Map, 1966 - 2015". USGS. U.S. Department of the Interior. Retrieved 2020-12-16.
  12. ^ a b "Baltimore Oriole, Icterus galbula". Audubon Bird Guide, North American Birds. 13 November 2014. Retrieved February 2, 2023.
  13. ^ Parnell, Marc (2021). Birds of New York (The Birding Pro's Field Guides). Naturalist & Traveler Press. p. 195. ISBN 9781954228146.
  14. ^ Bent, A. C. 1958. Life histories of North American blackbirds, orioles, tanagers, and allies. U.S. Natl. Mus. Bull. 211.
  15. ^ Schaefer, V. H. 1976. Geographic variation in the placement and structure of oriole nests. Condor 78:1976.
  16. ^ Foster, Mercedes S. (2007). "The potential of fruiting trees to enhance converted habitats for migrating birds in southern Mexico". Bird Conservation International. 17: 45–61. doi:10.1017/S0959270906000554.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Baltimore oriole: Brief Summary

provided by wikipedia EN

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. It is also the namesake and mascot for the Baltimore Orioles baseball team.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN