Seiurus aurocapilla

(Linnaeus, 1766)

Ovenbird

G5Secure Found in 72 roadless areas NatureServe Explorer →
G5SecureGlobal Rank
Least concernIUCN
MediumThreat Impact
Identity
Unique IDELEMENT_GLOBAL.2.103515
Element CodeABPBX10010
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryVertebrate Animal
IUCNLeast concern
Endemicoccurs (regularly, as a native taxon) in multiple nations
KingdomAnimalia
PhylumCraniata
ClassAves
OrderPasseriformes
FamilyParulidae
GenusSeiurus
Synonyms
Seiurus aurocapillus(Linnaeus, 1766)
Other Common Names
Chipe Suelero (ES) ovenbird (EN) Paruline couronnée (FR)
Concept Reference
American Ornithologists' Union (AOU). 1998. Check-list of North American birds. Seventh edition. American Ornithologists' Union, Washington, D.C. [as modified by subsequent supplements and corrections published in The Auk]. Also available online: http://www.aou.org/.
Taxonomic Comments
Formerly known as Seiurus aurocapillus, but changed for grammatical reasons (AOU 2003).
Conservation Status
Rank MethodExpertise without calculation
Review Date2016-04-09
Change Date1996-12-03
Edition Date2002-12-20
Edition AuthorsPALIS, J., revised by S. Cannings
Threat ImpactMedium
Range Extent>2,500,000 square km (greater than 1,000,000 square miles)
Number of Occurrences> 300
Rank Reasons
Large range; still common in many areas, though significant declines have occurred in some regions.
Range Extent Comments
BREEDING: northeastern British Columbia and southern Mackenzie to central Saskatchewan and Newfoundland, south to southern Alberta, western Montana, northern Nebraska, eastern Kansas, northern Alabama, and Carolinas; disjunct population in central Colorado (Van Horn and Donovan 1994, AOU 1998). NON-BREEDING: occasionally in U.S. in southern Texas, Gulf Coast, and North Carolina; most commonly in Mexico, along Pacific coast from Sinaloa south and along Atlantic coast from southern Tamaulipas south; also on Yucatan peninsula; less common throughout Central America, rarely to Colombia and Venezuela; also common in West Indies from central Bahamas to northern Lesser Antilles (fairly common in Puerto Rico and St. John); perhaps annual in Netherlands Antilles (Ridgely and Tudor 1989, Van Horn and Donovan 1994, AOU 1998).
Threat Impact Comments
SUMMARY: On the breeding grounds, forest fragmentation has resulted in increased Brown-headed Cowbird (MOLOTHRUS ATER) nest parasitism, increased nest predation by a variety of predators, and reduced pairing and reproductive success. Habitat is also lost or degraded, in the short-term, by clearcutting or other forms of timber harvest that open the canopy.

TIMBER HARVEST: Reduction of the forest canopy is also a threat. Forest thinning associated with recreational cottage construction in Ontario, fuelwood cutting in Massachusetts, and timber harvest in New York reduced habitat suitability (Chadwick et al. 1986, Clark et al. 1983, Webb et al. 1977). In Arkansas, restoration of Red-cockaded Woodpecker (PICOIDES BOREALIS) habitat (midstory hardwood removal followed by burning) eliminated Ovenbirds (Wilson et al. 1995). Habitat changes associated with waste-water irrigation can influence distribution.

This species apparently reaches higher densities than elsewhere in its range within the western boreal forest of Canada, and is threatened there by forest conversion to agriculture along the southern edges of the boreal zone. In Saskatchewan alone, 4368 square kilometers of forest was lost to agriculture in the period 1966-1994, a rate of -0.87%/year (Hobson et al. 2002). Much of the remaining southern boreal forest in western Canada has been leased to forestry companies (Cummings et al. 1994, Stelfox 1995). Deforestation is the primary threat to wintering birds.

NEST PARASITISM: Nests are parasitized by Brown-headed Cowbirds throughout the range (Van Horn and Donovan 1994). Percentage of parasitized nests range from 10% in Quebec (Terrill 1961) to 80% in Wisconsin (Brittingham and Temple 1983). Nest parasitism by Brown-headed Cowbirds decreases with increasing distance from the forest edge. Whereas nest parasitism was 100% within 99 meters of forest edge, it declined to zero 3300 meters from the edge (Brittingham and Temple 1983).

FOREST FRAGMENTATION: Frequency of Brown-headed Cowbird nest parasitism is also influenced by forest fragmentation. Frequency of nest parasitism by Brown-headed Cowbirds was lower in contiguous forested tracts in Missouri (2.5%) and Wisconsin and Minnesota (4%) than in forest fragments in Missouri (66.5%) and Wisconsin and Minnesota (19%; Donovan et al. 1995). In fragmented landscapes, Ovenbirds raise more Brown-headed Cowbirds than in unfragmented landscapes (Porneluzi and Faaborg 1999). Forest fragmentation also decreases male pairing success and nesting success (Burke and Nol 1998, Gibbs and Faaborg 1990, Porneluzi and Faaborg 1999, Porneluzi et al. 1993, Van Horn et al 1995, Villard et al. 1993). Male pairing success varies from zero in small forest fragments within an agricultural landscape to 100% in large tracts (Burke and Nol 1998). However, in managed-forest landscapes, forest fragmentation may not impair male pairing success (Sabine et al. 1996). Forest-dividing roads and powerline corridors can produce edge effects and reduce population density and/or male pairing success (Ortega and Capen 1999, Rich et al. 1994).

PREDATION: The predation rate of 14 nests in oak-hickory forest in Arkansas was 28.6% (Martin 1993). Nest predation may be affected by proximity to forest edge. In a forest fragment within an agricultural landscape, predation of artificial dome nests was significantly greater near the forest edge (<20 meters) than in the forest interior (200 and 400 meters from the edge; Linder and Bollinger 1995). Natural nests in similar forest fragments are also heavily predated (Donovan et al. 1995, Porneluzi et al. 1993). In managed-forest landscapes, however, proximity to edge may or may not influence nest predation. Whereas nesting success was negatively impacted by proximity to edge in a managed-forest landscape in New Hampshire (King et al. 1996), proximity to edge had no influence on nest success in similar habitat in Minnesota (Hanski et al. 1996). Nest predators include various snakes, the Blue Jay (CYANOCITTA CRISTATA), Brown-headed Cowbird, Red Squirrel (TAMIASCIURUS HUDSONICUS), Eastern Gray Squirrel (SCIURUS CAROLINENSIS), Raccoon (PROCYON LOTOR), Striped Skunk (MEPHITIS MEPHITIS), and weasel (MUSTELA sp.). Broad-winged Wawks (BUTEO PLATYPTERUS) prey on young and adults. Suspected predators include the Barred Oowl (STRIX VARIA), American Crow (CORVA BRACHYRHYNCHOS), Common Grackle (QUISCALUS QUISCULA), Deer Mouse (PEROMYSCUS MANICULATUS), Eastern Chipmunk (TAMIAS STRIATUS), Northern Flying Squirrel (GLAUCOMYS VOLANS), Virginia Opossum (DIDELPHIS VIRGINIANA), Red Fox (VULPES VULPES), Domestic Cat (FELIS DOMESTICUS) and Black Bear (URSUS AMERICANUS; Hahn 1937, Reitsma et al. 1990, Van Horn and Donovan 1994).

OTHER: Numerous individuals are killed by striking television towers and other similar tall structures during migration (Taylor and Kershner 1986). In Pennsylvania, less likely to inhabit tracts of forest irrigated with waste-water than non-irrigated forest (Yahner 1995).

WINTERING: On the wintering grounds threatened by deforestation, replacement of diverse native plant communities with agricultural and silvicultural monocultures, and subsistence hunting (Arendt 1992).
Ecology & Habitat

Description

A plump-looking, 15-cm-long bird with a thin pointed bill, pinkish legs, russet crowned bordered by darks stripes, bold white eye ring, olive dorsum, and white venter with bold dark streaks of spots (NGS 1983).

Habitat

BREEDING: Typically nests in mid-late successional, closed-canopied deciduous or deciduous-coniferous forests that have deep leaf litter and limited understory (Van Horn and Donovan 1994). Also nests in coniferous forest if deciduous forest is unavailable (Noon et al. 1980). Inhabited forest types include oak (QUERCUS)-hickory (CARYA), oak-pine (PINUS), maple (ACER)-basswood (TILIA), maple-birch (BETULA), maple-birch-beech (FAGUS GRANDIFOLIA), hemlock (TSUGA CANADENSIS)-oak, Trembling Aspen (POPULUS TREMULOIDES), and spruce (PICEA)-fir (ABIES) (Askins and Philbrick 1987, Freedman et al. 1981, Titterington et al. 1979, Van Horn and Donovan 1994, Westworth and Telfer 1993). Nests on the ground (Hahn 1937). In studies of regenerating forests following clearcutting, found to be absent from, or in low densities in, young, shrubby, open-canopied stands; whereas they occurred in relative abundance in older, closed-canopied stands (Freedman et al. 1981, Thompson et al. 1992, Titterington et al 1979, Webb et al. 1977, Westworth and Telfer 1993).

NON-BREEDING: In the Caribbean region, utilizes a variety of habitats including coastal dry forest, elfin woodland, forest edge, pine forests, riparian forests, wet forests, wetlands, and urban areas (Arendt 1992). In Costa Rica, inhabits primary and secondary forest (Blake and Loiselle 1992); prefers shady understory of forest with well-developed shrub layer (Stiles and Skutch 1989). In Puerto Rico and surrounding islands, occurs in interior forests as well as mangroves and dry thickets (Raffaele 1989). Considered a forest generalist on the Yucatan Peninsula (Lynch 1989), and captured with equal frequency in primary and secondary forest in Veracruz (Rappole et al. 1992). In the Virgin Islands, inhabits both moist and dry evergreen forest, as well as transition zones between these forest types (Askins et al. 1992). Low numbers inhabit coffee, citrus, cacao, and pine plantations in Puerto Rico, Jamaica, Belize and Costa Rica (Robbins et al. 1992). Captured most frequently in pine savanna in Belize (Petit et al. 1992).

Ecology

TERRITORY SIZE/DENSITY: Territory size and male density varies with prey abundance and size of inhabited forest. Territory size of 13 males studied in Ontario ranged from 0.6-1.6 hectares (mean = 0.8) and inversely correlated with the biomass of invertebrate prey, with territory size decreasing as prey biomass increased (Stenger 1958). A negative correlation between territory size and prey abundance was also observed in Tennessee (Smith and Shugart 1987). In Ontario, territory size was significantly smaller during a spruce budworm (CHORISTONEURA FUMIFERANA) outbreak than during non-budworm years (Zach and Falls 1975). Also territorial on the wintering grounds (Rappole and Warner 1980).

In Ontario, densities of males ranged from 0.33-8.3/10 hectares, and increased significantly with increasing woodlot core area (core area is forest 3100 meters from the forest edge; Burke and Nol 1998). In central Missouri, male population density ranged from 0.66-1.73/10 hectares, and increased with increasing forest size (Wenny et al. 1993). Density of males was positively related to size of forest tract and core area in eastern Pennsylvania, ranging from 1.3-7.2 males/10 hectares (Porneluzi et al. 1993). In a managed-forest landscape in New Brunswick, density of males in forest fragments (1.1/10 ha) did not differ statistically from a large contiguous forested tract (1.9/10 ha; Sabine et al. 1996). In northern hardwood forest in New Hampshire, average population density was 13.5 birds/10 hectares (Sabo and Holmes 1983).

SITE FIDELITY: Exhibits breeding site fidelity. In Illinois, 3 of 8 (37.5%) of those banded one year were recaptured the subsequent year (Robinson 1992). Of 22 adults and 40 young banded one year in Michigan, 10 adults (45%) and one yearling (2.5%) returned to the study area the following year. The three returning males occupied their former territory, whereas females either returned to their former territory or occupied an adjacent territory. The following year, the three males again returned and occupied their former territories (Hahn (1937). In New Jersey, 36% of adults and 10% of young banded in one year returned the following year (Leck et al. 1988). In Missouri, an average of 41% of males banded one year returned the next; 64% had second-year territories with >50% overlap with first-year territories, and 26% were adjacent to or overlapped <50% with the territory of the previous year (Porneluzi and Faaborg 1999). Also exhibits site fidelity to wintering grounds (Faaborg and Arendt 1984, Kricher and Davis 1986, Martin and Carr 1986).

POPULATION PARAMETERS: Annual survivorship of birds in Pennsylvania and Michigan was estimated to be 54% (Hahn 1937, Savidge and Davis 1974 cited in Van Horn and Donovan 1994). Overwinter survival rates did not differ between mature and early-successional forests in Belize (Conway et al. 1995). Oldest known individual was 9 years old (Dowell and Robbins 1998).

PARASITES: Adults are host to six species of external parasites, including two lice (MENACANTHUS CHRYSOPHAEUM, MYRSIDEA INCERTA), three ticks (HAEMAPHYSALIS LEPORISPALUSTRIS, IXODES BRUNNEUS, IXODES DAMMINI), and one mite (LIPONYSSUS SYLVIARIUM; Peters 1936 cited in Van Horn and Donovan 1994). Mites have also been found on nestlings (Hahn 1937).

Reproduction

PHENOLOGY: Nests from May-July (Terres 1991). First breeds in the spring after hatching (Van Horn and Donovan 1994).

OVIPOSITION/INCUBATION: Typically produces one clutch per year, although sometimes two or three (Hahn, 1937, Zach and Falls 1975). Average clutch size for 27 nests in Michigan was 4.7 eggs (range = 3-6). First clutches typically had five eggs, subsequent clutches 3-5 (Hahn 1937; statistically significant difference between first and later clutches; Zach and Falls 1975). Mean clutch size of 78 clutches was 4.4 eggs (Van Horn and Donovan 1994). A female that nested three times in one season in Michigan laid a total of 10 eggs (Hahn 1937), another in Ontario laid 13 eggs (Zach and Falls 1975). Eggs are laid every other day and incubation begins after the penultimate egg is laid (Hahn 1937). Females alone incubate the eggs and brood the young. Incubation period ranges from 11.5-14 days (mean = 12.25).

FLEDGING: Young leave the nest when 6.5-8.5 days old (mean = 8), and are capable of flight at 11 days old (Hahn 1937). Both parents feed the young. The brood is typically divided between the parents after the young leave the nest.

NEST SUCCESS: In Michigan, 63.4% of eggs hatched and 43.5% of young fledged (Hahn 1937); in Minnesota, nest success (fledged at least one young) ranged from 75-100% (Hanski, et al. 1996) and in Arkansas, it was 71.4% (Martin 1993).
Terrestrial Habitats
Forest - HardwoodForest - MixedWoodland - HardwoodWoodland - MixedShrubland/chaparral
Palustrine Habitats
Riparian
Other Nations (2)
CanadaN5B
ProvinceRankNative
British ColumbiaS5BYes
QuebecS5BYes
Yukon TerritoryS2BYes
Northwest TerritoriesS5Yes
Island of NewfoundlandS3B,SUMYes
AlbertaS5BYes
New BrunswickS5BYes
SaskatchewanS5BYes
Nova ScotiaS5BYes
Prince Edward IslandS5BYes
ManitobaS5BYes
OntarioS5BYes
United StatesN5B
ProvinceRankNative
ConnecticutS5BYes
TexasS4Yes
TennesseeS4Yes
OhioS5Yes
PennsylvaniaS5BYes
WisconsinS5BYes
ColoradoS2BYes
AlabamaS4B,S2NYes
WashingtonSNAYes
IowaS4B,S4NYes
VirginiaS5Yes
South DakotaS3BYes
MississippiS1BYes
West VirginiaS5BYes
OklahomaS2BYes
NebraskaS4Yes
North DakotaSNRBYes
New HampshireS5BYes
MichiganS5Yes
MinnesotaSNRBYes
KentuckyS5BYes
New YorkS5BYes
New JerseyS4B,S4NYes
MissouriSNRBYes
South CarolinaS5Yes
LouisianaSNAYes
ArkansasS4BYes
DelawareS5BYes
IdahoSNAYes
Rhode IslandS5BYes
ArizonaS2MYes
GeorgiaS5Yes
WyomingS3BYes
District of ColumbiaS2B,S3NYes
MontanaS4BYes
KansasS1BYes
North CarolinaS5B,S1NYes
MaineS5B,S5MYes
MassachusettsS5BYes
VermontS5BYes
New MexicoS4NYes
MarylandS5BYes
IndianaS4BYes
IllinoisS4Yes
FloridaSNAYes
Roadless Areas (72)
Arizona (1)
AreaForestAcres
TumacacoriCoronado National Forest44,594
Arkansas (2)
AreaForestAcres
East ForkOzark-St. Francis National Forest13,037
Pedestal RocksOzark-St. Francis National Forest21,957
California (1)
AreaForestAcres
Benton RangeInyo National Forest9,637
Florida (1)
AreaForestAcres
Farles PrairieOcala National Forest1,901
Georgia (3)
AreaForestAcres
Lance CreekChattahoochee National Forest9,025
Pink KnobChattahoochee National Forest12,127
Tripp BranchChattahoochee National Forest615
Michigan (1)
AreaForestAcres
Bear SwampHuron-Manistee National Forest3,915
Montana (1)
AreaForestAcres
Big Snowy Mountains WsaLewis and Clark National Forest88,003
New Hampshire (11)
AreaForestAcres
Carr MountainWhite Mountain National Forest17,110
Cherry MountainWhite Mountain National Forest8,766
Great Gulf Ext.White Mountain National Forest15,110
KearsargeWhite Mountain National Forest4,554
KilkennyWhite Mountain National Forest28,766
Kinsman MountainWhite Mountain National Forest8,999
PemigewassetWhite Mountain National Forest32,255
Pemigewasset ExtWhite Mountain National Forest15,840
Presidential - Dry River ExtWhite Mountain National Forest10,555
Sandwich RangeWhite Mountain National Forest16,797
Wild RiverWhite Mountain National Forest46,878
New Mexico (1)
AreaForestAcres
South Guadalupe MountainsLincoln National Forest20,930
North Carolina (12)
AreaForestAcres
Barkers Creek (addition)Nantahala National Forest975
Big Indian (addition)Nantahala National Forest1,155
Chunky Gal (addition)Nantahala National Forest3,336
Harper CreekPisgah National Forest7,325
Jarrett CreekPisgah National Forest7,485
Laurel MountainPisgah National Forest5,683
Little Indian (addition)Nantahala National Forest640
Lost CovePisgah National Forest5,944
Mackey MountainPisgah National Forest5,934
Overflow CreekNantahala National Forest3,379
SnowbirdNantahala National Forest8,489
Woods MountainPisgah National Forest9,602
North Dakota (2)
AreaForestAcres
Long X DivideDakota Prairie Grasslands10,099
Ponderosa PineDakota Prairie Grasslands7,471
Pennsylvania (1)
AreaForestAcres
Minister ValleyAllegheny National Forest1,417
Tennessee (3)
AreaForestAcres
Devil's BackboneCherokee National Forest4,287
Sampson Mountain AdditionCherokee National Forest3,064
Sycamore CreekCherokee National Forest6,984
Vermont (1)
AreaForestAcres
Bread LoafGreen Mountain and Finger Lakes National Forests1,768
Virginia (22)
AreaForestAcres
Adams PeakGeorge Washington National Forest7,135
Bear CreekJefferson National Forest18,274
Beards MountainGeorge Washington National Forest7,505
Broad RunJefferson National Forest10,971
Brush MountainJefferson National Forest6,002
Dolly AnnGeorge Washington National Forest7,855
Elliott KnobGeorge Washington National Forest9,380
Hoop HoleJefferson National Forest4,652
Laurel ForkGeorge Washington National Forest9,967
Little RiverGeorge Washington National Forest27,292
Little Wilson Creek Addition BJefferson National Forest1,725
Mt. PleasantGeorge Washington National Forest8,933
North MountainJefferson National Forest8,377
Northern MassanuttenGeorge Washington National Forest9,444
Peters Mountain Addition BJefferson National Forest2,909
Raccoon BranchJefferson National Forest4,388
Ramseys Draft AdditionGeorge Washington National Forest12,781
Saint Marys AdditionGeorge Washington National Forest1,454
Seng MountainJefferson National Forest6,428
Shawvers Run AdditionJefferson National Forest1,927
The PriestGeorge Washington National Forest5,737
Three RidgesGeorge Washington National Forest4,745
West Virginia (8)
AreaForestAcres
Cranberry AdditionMonongahela National Forest11,123
Cranberry Glades Botanical AreaMonongahela National Forest785
Dolly Sods Roaring PlainMonongahela National Forest13,392
Dry River (WV)George Washington National Forest7,331
Falls Of Hills CreekMonongahela National Forest6,925
Little MountainMonongahela National Forest8,172
Middle MountainMonongahela National Forest19,020
North Mountain HopevilleMonongahela National Forest6,525
Wyoming (1)
AreaForestAcres
Piney CreekBighorn National Forest22,240
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