Breeding bird assemblages supported by developing upland shrub woodland are influenced by microclimate and habitat structure

Bird Study ◽  
2019 ◽  
Vol 66 (2) ◽  
pp. 178-186
Author(s):  
John Calladine ◽  
David Jarrett ◽  
Mark Wilson
2005 ◽  
Vol 147 (3) ◽  
pp. 419-427 ◽  
Author(s):  
Nikos Katsimanis ◽  
Michalis Dretakis ◽  
Triantaphyllos Akriotis ◽  
Moysis Mylonas

2018 ◽  
Vol 24 (7) ◽  
pp. 928-938 ◽  
Author(s):  
Frank A. La Sorte ◽  
Christopher A. Lepczyk ◽  
Myla F. J. Aronson ◽  
Mark A. Goddard ◽  
Marcus Hedblom ◽  
...  

Bird Study ◽  
2006 ◽  
Vol 53 (3) ◽  
pp. 225-236 ◽  
Author(s):  
Mark W. Wilson ◽  
Josephine Pithon ◽  
Tom Gittings ◽  
Tom C. Kelly ◽  
Paul S. Giller ◽  
...  

1989 ◽  
Vol 34 (4) ◽  
pp. 487 ◽  
Author(s):  
Dale W. Stahlecker ◽  
Patricia L. Kennedy ◽  
Anne C. Cully ◽  
Charles B. Kuykendall

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e8898
Author(s):  
Peter Pyle ◽  
Kenneth R. Foster ◽  
Christine M. Godwin ◽  
Danielle R. Kaschube ◽  
James F. Saracco

Landbird vital rates, such as productivity and adult survivorship, can be estimated by modeling mist-netting capture data. The proportion in which an adult breeding bird is 1 year of age (a “yearling”), however, has been studied only minimally in a few landbird species. Here we relate yearling proportion to habitat-structure covariates, including reclamation age, in a boreal forest landbird community. Data were collected at 35 constant-effort mist-netting stations over a 6-year period, and consisted of 12,714 captures of adults, of 29 landbird species, including 4,943 captures of yearlings. Accuracy of age determination (yearling or older) was assessed based on recapture data and error rates were estimated at a mean of 8.1% (range 0.0–19.4%) among the 29 species, with 20 species showing age-error rates <10%. The estimated mean yearling proportion was 0.407, ranging from 0.178 to 0.613 among species. Remote-sensed Enhanced Vegetation Index (EVI), a measure of habitat greenness, was positively correlated with age since reclamation up to 20 years, at which time it became comparable to that of natural stations. The probability of capturing a yearling for species associated with mature forest was lower at stations with higher EVI and the opposite was the case for species favoring successional habitats. These results suggest that yearling birds are being excluded from preferred breeding habitats by older birds through despotism and/or that yearlings are simply selecting poorer habitat due to lack of breeding experience or other factors. This dynamic appears to be operating in multiple species within this forest landbird community. Captured yearlings may also be “floaters”, or non-breeding individuals not holding territories. However, presuming that yearlings show lower reproductive success whether floating or not, our results suggest that stations with high yearling proportions could be located within sink as opposed to source habitats. Overall, we infer that yearling proportion may become an important vital-rate measure of habitat quality and reclamation efforts, when combined with indices of population size, productivity, reproductive condition and survivorship.


1994 ◽  
Vol 343 (1304) ◽  
pp. 135-144 ◽  

We examine the relation between body size, abundance, and taxonomy in the wintering bird assemblages in Britain and Ireland. The regression slope of abundance on body size across species in both assemblages is not significantly different from that predicted by an ‘energetic equivalence rule’, but the proportion of the variance in abundance explained by body size is very low. Previous work on breeding bird assemblages has found the novel relation that the correlation between size and abundance across species within a tribe is itself positively correlated with the degree of taxonomic isolation of the tribe from other tribes in the bird fauna. We show that the same relation holds within bird tribes in the two wintering assemblages. Furthermore, evidence for this relation is found by using two different measures of bird abundance, despite these two abundance measures showing very different correlations with body size across species. Although these patterns in the data are consistent, some are not formally statistically significant ( p = 0.089 or greater). Excluding coastal, stocked, feral and recently colonizing species increased the significance of time since origin of a tribe on species abundances. We conclude that the relation between size and abundance in bird tribes is somehow related to bird taxonomy. While acknowledging the unlikely nature of such an effect, we tentatively propose hypotheses for two mechanisms that could produce the observed patterns.


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