Academic literature on the topic 'Black-capped chickadee'

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Journal articles on the topic "Black-capped chickadee"

1

Snell, Cara L., Stefanie E. LaZerte, Matthew W. Reudink, and Ken A. Otter. "Sympatric song variant in mountain chickadees Poecile gambeli does not reduce aggression from black-capped chickadees Poecile atricapillus." European Journal of Ecology 2, no. 1 (2016): 53–59. http://dx.doi.org/10.1515/eje-2016-0006.

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Abstract When habitats overlap and species compete for resources, negative interactions frequently occur. Character displacement in the form of behavioural, social or morphological divergences between closely related species can act to reduce negative interactions and often arise in regions of geographic overlap. Mountain chickadees Poecile gambeli have an altered song structure in regions of geographic overlap with the behaviourally dominant black-capped chickadee Poecile atricapillus. Similar to European and Asian tits, altered song in mountain chickadees may decrease aggression from black-c
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2

Bloomfield, Laurie L., Leslie S. Phillmore, Ronald G. Weisman, and Christopher B. Sturdy. "Note types and coding in parid vocalizations. III: The chick-a-dee call of the Carolina chickadee (Poecile carolinensis)." Canadian Journal of Zoology 83, no. 6 (2005): 820–33. http://dx.doi.org/10.1139/z05-067.

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Species of the genus Poecile Kaup, 1829 (the chickadees) are well suited to comparative studies of acoustic communication because their songs and calls occur in similar contexts and are acoustically similar. Here we provide careful, reliable descriptions and spectrographic exemplars for seven note types observed in the chick-a-dee calls of the Carolina chickadee, Poecile carolinensis (Audubon, 1834). The note types include A, C, and D notes similar to those found in the chick-a-dee calls of the black-capped chickadee, Poecile atricapillus (L., 1766), a complex of three B-note subtypes (B1, B2,
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3

Reudink, Matthew W., Stephen G. Mech, Sean P. Mullen, and Robert L. Curry. "Structure and Dynamics of The Hybrid Zone Between Black-Capped Chickadee (Poecile Atricapillus) and Carolina Chickadee (P. Carolinensis) in Southeastern Pennsylvania." Auk 124, no. 2 (2007): 463–78. http://dx.doi.org/10.1093/auk/124.2.463.

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AbstractAnalysis of the structure and stability of a hybrid zone can serve as a starting point for examining mechanisms that influence spatial and evolutionary relationships between species. Recent studies of the hybrid zone between Black-capped Chickadee (Poecile atricapillus) and Carolina Chickadee (P. carolinensis) have suggested that genetic introgression is limited to a narrow zone, while also reinforcing the conclusion that the line of contact between these parapatrically distributed species is now shifting northward. We investigated the structure, position, and recent movement of the ch
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4

Mack, Andrew L., Frank B. Gill, Robert Colburn, and Christina Spolsky. "Mitochondrial DNA: A Source of Genetic Markers for Studies of Similar Passerine Bird Species." Auk 103, no. 4 (1986): 676–81. http://dx.doi.org/10.1093/auk/103.4.676.

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Abstract Restriction enzyme analyses of mitochondrial DNA (mtDNA) of the Black-capped Chickadee (Parus atricapillus), Carolina Chickadee (P. carolinensis), and Tufted Titmouse (P. bicolor) indicate substantial genetic divergence (p = 0.04-0.09). Eleven of 14 enzymes produced fragment patterns that distinguish the two chickadees, revealing a bounty of markers for studies of these sibling species.
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5

Brodin, Anders. "Hippocampal Volume Does not Correlate With Food-Hoarding Rates in The Black-Capped Chickadee (Poecile Atricapillus) and Willow Tit (Parus Montanus)." Auk 122, no. 3 (2005): 819–28. http://dx.doi.org/10.1093/auk/122.3.819.

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Abstract Food-hoarding birds use memory to relocate caches, and species that store thousands of scattered food items must have an extraordinary memory capacity to be able to relocate them. Because the hippocampus is important in the functioning of spatial memory, it is logical to assume that the amount of food stored should correlate with hippocampal volume. Previously, food-hoarding capacity has been used as the predictor variable for hippocampal volume. Using the opposite approach, I tested whether hippocampal volume can be used to predict the amount of food stored. The atricapilla complex,
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6

Fotheringham, James R., and Laurene Ratcliffe. "Song degradation and estimation of acoustic distance in Black-capped Chickadees (Parus atricapillus)." Canadian Journal of Zoology 73, no. 5 (1995): 858–68. http://dx.doi.org/10.1139/z95-101.

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Black-capped Chickadees (Parus atricapillus) sing a two-note song termed fee bee. Frequency descends within the fee note and between the fee and bee notes. Within-song frequency ratios are highly invariant, while among songs, absolute frequency is variable. We conducted sound-transmission studies to analyze how Black-capped Chickadee songs degrade in different native habitats. We then subjected colour-banded territorial males to playback of undegraded and degraded songs to see if they could estimate the distance to a conspecific singer by means of degradation cues. In transmission studies cond
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7

Lait, Linda A., Randy F. Lauff, and Theresa M. Burg. "Genetic Evidence Supports Boreal Chickadee (Poecile hudsonicus) × Black-capped Chickadee (Poecile atricapillus) Hybridization in Atlantic Canada." Canadian Field-Naturalist 126, no. 2 (2012): 143. http://dx.doi.org/10.22621/cfn.v126i2.1330.

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Both morphological and genetic evidence support a hybridization event between a Boreal Chickadee (Poecile hudsonicus) and a Black-capped Chickadee (Poecile atricapillus) in Atlantic Canada. Plumage of the hybrid was intermediate to both parental species, with buffy sides and a dark brown cap on the head. Mitochondrial DNA control region showed the female lineage to be from a Boreal Chickadee, while Z-linked markers showed mixed Boreal Chickadee × Black-capped Chickadee heritage, likely representing an F1 hybrid. This is the first documented case of hybridization between these species in easter
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8

Proppe, D. S., K. A. Byers, C. B. Sturdy, and C. C. St. Clair. "Physical condition of Black-capped Chickadees (Poecile atricapillus) in relation to road disturbance." Canadian Journal of Zoology 91, no. 11 (2013): 842–45. http://dx.doi.org/10.1139/cjz-2013-0081.

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Roads and their associated low-frequency noise have been linked with a reduction in abundance and density for many songbird species. However, a handful of species remain equally abundant in roadside habitats and nondisturbed areas. Abundance is a valuable baseline indicator of a species’ ability to adapt to habitats altered by roads, but does not directly ascertain whether health is affected in these species. Here we examine whether Black-capped Chickadees (Poecile atricapillus (L., 1766)), a species that remains abundant near roads, exhibit higher levels of chronic stress or reduced physical
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9

Ingolfsson, Vala, Carolina Montenegro, William D. Service, and Christopher B. Sturdy. "Manual versus automatic identification of black-capped chickadee (Poecile atricapillus) vocalizations." Alberta Academic Review 2, no. 2 (2019): 41–42. http://dx.doi.org/10.29173/aar48.

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One time-consuming aspect of bioacoustic research is identifying vocalizations from long audio recordings. SongScope (version 4.1.5. Wildlife Acoustics, Inc.) is a computer program capable of developing acoustic recognizers that can identify wildlife vocalizations. The goal of the current study was to compare the effectiveness of manual identification of black-capped chickadee vocalizations to identification by SongScope recognizers. A recognizer was developed for each main chickadee vocalization by providing previously annotated audio of chickadees. Six chickadees (three male, three female) w
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10

Bronson, C. L., Thomas C. Grubb, Gene D. Sattler, and Michael J. Braun. "Reproductive Success Across The Black-Capped Chickadee (Poecile Atricapillus) and Carolina Chickadee (P. Carolinensis) Hybrid Zone in Ohio." Auk 122, no. 3 (2005): 759–72. http://dx.doi.org/10.1093/auk/122.3.759.

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AbstractBlack-capped Chickadees (Poecile atricapillus) and Carolina Chickadees (P. carolinensis) hybridize in an east-west band from New Jersey to Kansas. Within the past century, the Ohio portion of this hybrid zone and the Carolina Chickadee range to the south have been moving northward, whereas the Black-capped Chickadee range has retracted. In Ohio, we characterized the genetic composition of the hybrid zone using five diagnostic molecular loci. Although there was no evidence of assortative mating in the center of the hybrid zone, we found a relative paucity of genetically intermediate bre
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