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The Hair-crested Drongo (Dicrurus hottentottus) exhibits a unique nest-dismantling behavior after the fledging of the young. One hypothesis explaining this behavior is dismantling one's own nest may reduce potential competition for nest sites in the following breeding season because suitable breeding habitat might be limited,and sites are often reused.
By comparing the habitat features at nest and random locations,we determined the nest habitat preference of the Hair-crested Drongo within Dongzhai National Nature Reserve,Henan,China. We also compared habitat features with nesting success to determine if any trends could be detected.
We found that nest tree height,diameter at breast height,live crown ratio,tree rank,and presence of overstory were significantly higher at nesting locations than random locations; slope,leaf litter cover percentage and depth,presence of understory and midstory,and number of trees per hectare were significantly lower at nest sites than random sites. Drongos preferrAed to use some tree species,such as Metasequoia glyptostroboides,Castanea mollissima,and Pterocarya stenoptera for nesting. Failed nests were often associated with habitat with higher percentage of leaf litter on the ground.
Our data support that selection of nest sites does occur for this species at this site and therefore support the hypothesis that breeding habitat limitation could be one of the driving forces for the development of the nest-dismantling behavior in this species.
The Hair-crested Drongo (Dicrurus hottentottus) exhibits a unique nest-dismantling behavior after the fledging of the young. One hypothesis explaining this behavior is dismantling one's own nest may reduce potential competition for nest sites in the following breeding season because suitable breeding habitat might be limited,and sites are often reused.
By comparing the habitat features at nest and random locations,we determined the nest habitat preference of the Hair-crested Drongo within Dongzhai National Nature Reserve,Henan,China. We also compared habitat features with nesting success to determine if any trends could be detected.
We found that nest tree height,diameter at breast height,live crown ratio,tree rank,and presence of overstory were significantly higher at nesting locations than random locations; slope,leaf litter cover percentage and depth,presence of understory and midstory,and number of trees per hectare were significantly lower at nest sites than random sites. Drongos preferrAed to use some tree species,such as Metasequoia glyptostroboides,Castanea mollissima,and Pterocarya stenoptera for nesting. Failed nests were often associated with habitat with higher percentage of leaf litter on the ground.
Our data support that selection of nest sites does occur for this species at this site and therefore support the hypothesis that breeding habitat limitation could be one of the driving forces for the development of the nest-dismantling behavior in this species.
Dow DD. Breeding biology and development of the young of Manorina melanocephala, a communally breeding Honeyeater. Emu. 1978;78:207-22.
Gao ZJ, Du ZY, Wang XS, Huang H, Wang K, Yang CB. The nest-site selection of Hair-crested Drongo Dicrurus hottentottus. Chin J Zool. 2006;41:69-73.
Holmes RT, Robinson SK. Spatial patterns, foraging tactics, and diets of ground-foraging birds in a northern hardwoods forest. Wilson Bull. 1988;100:377-94.
James FC, Shugart HH Jr. A quantitative method of habitat description. Audubon Field Notes. 1970;24:727-36.
Kershner EL, Bollinger EK, Helton MN. Nest-site selection and renesting in Blue-gray Gnatcatchers (Polioptila caerulea). Am Midl Nat. 2001;146:404-13.
Li J, Lin S, Wang Y, Zhang Z. Nest-dismantling behavior of the Hair-crested Drongo in central China: an adaptive behavior for increasing fitness? Condor. 2009;111:197-201.
Lonsdale WM. Predicting the amount of litter fall in the forests of the world. Ann Bot. 1988;61:319-24.
Misenhelter MD, Rotenberry JT. Choices and consequences of habitat occupancy and nest site selection in sage sparrows. Ecology. 2000;81:2892-901.
Sedgwick J, Knopf FL. A high incidence of Brown-headed cowbird parasitism of Willow Flycatchers. Condor. 1988;90:253-6.
Spain AV. Literfall and the standing crop of litter in three tropical Australian rainforests. J Ecol. 1984;72:947-61.
Van Wilgenburg SL, Mazerolle DF, Hobson KA. Patterns of arthropod abundance, vegetation, and microclimate at boreal forest edge and interior in two landscapes: implications for forest birds. Ecoscience. 2001;8:454-61.
Xu JL, Zhang ZW, Zheng GM, Zhang XH, Sun WH, McGowan P. Home range and habitat use of Reeve's Pheasant Syrmaticus reevesii in the protected areas created from forest farms in the Dabie Mountains, central China. Bird Conserv Int. 2007;17:319-30.
Zheng GM. A checklist of the classification and distribution of the birds of China. Beijing: Science Press; 2011.
We appreciate the support by Dongzhai National Nature Reserve for conducting this study. Funding and support was provided by National Science Foundation East Asia Pacific Summer Institute (EAPSI), Chinese Ministry of Science and Technology, and China Science and Technology Exchange Center. Further funding and support was provided by Alabama A&M University and Beijing Normal University. We want to express our gratitude to Antillo Biancucci, Matthew Lerow, Peng Zhang, and Langyu Gu for their assistance in and out of the field.
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