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Research | Open Access

Nest distribution and nest habitat of the Tibetan Partridge (Perdix hodgsoniae) near Lhasa, Tibet

Tsering Dorge1,2Göran Högstedt1Terje Lislevand3( )
Department of Biology, University of Bergen, Box 7803, 5020 Bergen, Norway
Department of Biology, Faculty of science, Tibet University, 850000 Lhasa, Chinas
University Museum of Bergen, University of Bergen, Box 7800, 5020 Bergen, Norway
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Abstract

Background

Little is hitherto known about the breeding ecology of the Tibetan Partridge (Perdix hodgsoniae) which is endemic to the Tibetan plateau. Here we describe nest densities, inter-nest distances and general nest site characteristics in this gallinaceous bird species and explore the possibilities that certain shrub and plant types are preferred as nest surroundings.

Method

A total of 56 nests were found over three breeding seasons near Lhasa, Tibet. Nest site characteristics were compared with random control plots and the proportions of specific plant species covering nests were compared with their estimated general occurrence in the study area.

Results

Nest density in the two years with highest search effort was estimated at 1.43/km2 and 1.04/km2 but was clearly higher in the part of the study area facing north (1.86-2.35/km2) than that facing south (0.11-0.34/ km2). The average nearest neighbour distance of nests was about 300 m. Nests were situated in relatively lush vegetation and covered by a total of eight shrub species and three herbs. In contrast to previous reports, Caragana shrub did not constitute an important part of the nest habitat. The flowering, non-thorny bush Potentilla fruticosa was significantly over-represented as nest cover, while Rhododendron nivale was similarly under-represented. Nest bush foliage covered a larger area of ground, and the shrub surrounding nests was generally denser, than in control samples. Also, nests were placed closer to paths and in areas with lower densities of Yak (Bos grunniens) dung than in control samples. Except that soil temperatures were lower on nest sites than on control sites, micro-climate variables measured in this study did not differ between nest sites and control plots.

Conclusions

Opportunity for nest concealment is probably an important quality of the nest habitat in Tibetan Partridges, yet it is unclear why the species should prefer P. fruticosa as nest cover. It is possible that nest sites are chosen to secure escape exits in the case of approaching predators and to reduce the risk of nest trampling. Tibetan Partridges may also select nest sites according to micro-climate, either directly or indirectly through climate-related differences in shrub vegetation.

References

 

Amat J, Masero JA (2004) Predation risk on incubating adults constrains the choice of thermally favourable nest sites in a plover. Anim Behav 67:293–300

 

ASAB (2012) Guidelines for the treatment of animals in behavioural research and teaching. Anim Behav 83:301–309

 

Beintema AJ, Müskens GJDM (1987) Nesting success of birds breeding in Dutch agricultural grasslands. J Appl Ecol 24:743–758

 
BirdLife International (2014) Species factsheet: Perdix hodgsoniae. [http://www.birdlife.org on 07/01/2014]
 

Burhans DE, Thompson FR (2001) Relationship of songbird nest concealment to nest fate and flushing behavior of adult. Auk 118:237–242

 

D'Alba L, Spencer KA, Nager RG, Monaghan P (2011) State dependent effects of elevated hormone: Nest site quality, corticosterone levels and reproductive performance in the common eider. Gener Compar Endocrinol 172:218–224

 

Deeming DC (2002) Avian Incubation: Behaviour, Environment, and Evolution. Oxford University Press, Oxford

 
del Hoyo J, Elliott A, Sargatal J (1994) Handbook of the Birds of the World, vol 2. Lynx Edicions, Barcelona
 

DeLong AK, Crawford JA, Delong DC Jr (1995) Relationships between vegetational structure and predation of artificial Sage Grouse nests. J Wildlife Manage 59:88–92

 

Dion N, Hobson KA, Larivière S (2000) Interactive effects of vegetation and predators on the success of natural and simulated nests of grassland songbirds. Condor 102:629–634

 
Dorge T (2014) Nesting ecology in a Himalayan gallinaceous bird, the Tibetan Partridge (Perdix hodgsoniae). PhD thesis. University of Bergen,
 

Eggers S, Griesser M, Nystrand M, Ekman J (2006) Predation risk induces changes in nest-site selection and clutch size in the Siberian jay. Proc R Soc B 273:701–706

 

Filliater TS, Breitwisch R, Nealen PM (1994) Predation on Northern Cardinal Nests: Does choice of nest site matter? Condor 96:761–768

 

Götmark F, Blomqvist D, Johansson OC, Bergkvist J (1995) Nest-site selection: a trade-off between concealment and view of the surroundings? J Avian Biol 26:305–312

 
Ivlev VS (1961) Experimental Ecology of the Feeding of Fishes. Yale University Press, New Haven, Connecticut
 

Johnsgard PA (1988) The Quails, Partridges and Francolins of the World. Oxford University Press, Oxford

 

Kim S-Y, Monaghan P (2005) Effects of vegetation on nest microclimate and breeding performance of lesser black-backed gulls (Larus fuscus). J Ornithol 146:176–183

 

Koerth BH, Webb WM, Bryant FC, Guthery FC (1983) Cattle trampling of simulated ground nests under short duration and continuous grazing. J Range Manage 36:385–386

 

Kutiel P (1992) Slope aspect effect on soil and vegetation in a Mediterranean ecosystem. Israel J Botany 41:243–250

 

Larison B, Laymon SA, Williams PL, Smith TB (1998) Song Sparrows vs. cowbird brood parasites: impacts of forest structure and nest-site selection. Condor 100:93–101

 

Lima S (2009) Predators and the breeding bird: behavioral and reproductive flexibility under the risk of predation. Biol Rev 84:485–513

 

Loye JE, Carroll SP (1998) Ectoparasite behavior and its effects on avian nest site selection. Ann Entomol Soc Am 91:159–163

 

Lu X, Gong GH, Ci R (2003) Reproductive ecology of the Tibetan partridge Perdix hodgsoniae in Lhasa Mountains. Tibet J Yamashina Inst Ornithol 34:270–278

 

Lu X, Ke D, Ma X, Gong G, Yu T (2010) Nesting records of 20 bird species in Lhasa region, Tibet. Chinese Birds 1:167–174

 
Madge S, McGowan P (2002) Pheasants, Partridges and Grouse. Cristopher Helm, London
 

Magaña M, Alonso JC, Martin CA, Bautista LM, Martin B (2010) Nest-site selection by Great Bustards Otis tarda suggests a trade-off between concealment and visibility. Ibis 152:77–89

 

Martin TE (1993) Nest predation and nest sites: new perspectives on old patterns. Bioscience 43:523–532

 

Martin TE (1995) Avian life history evolution in relation to nest sites, nest predation, and food. Ecol Monogr 65:101–127

 

Marzluff JM (1988) Do pinyon jays alter nest placement based on prior experience? Anim Behav 36:1–10

 

Montevecchi MA (1978) Nest site selection and its survival value among laughing gulls. Behav Ecol Sociobiol 4:143–161

 

Paine L, Undersander DJ, Sample DW, Bartelt GA, Schatteman TA (1996) Cattle trampling of simulated ground nests in rotationally grazed pastures. J Range Manage 49:294–300

 
Potts GR (2012) Partridges. Collins, London
 
R Core Team (2010) R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria (http://www.R-project.org)
 

Rands MRW (1988) The effect of nest site selection on nest predation in Grey Partridge Perdix perdix and Red-legged Partridge Alectoris rufa. Ornis Scand 19:35–40

 

Remeš V (2005) Nest concealment and parental behaviour interact in affecting nest survival in the blackcap (Sylvia atricapilla): an experimental evaluation of the parental compensation hypothesis. Behav Ecol Sociobiol 58:326–333

 
Siegel S, Castellan NJ (1988) Nonparametric Statistics for the Behavioral Sciences. McGraw-Hill International Editions, New York
 

Storey AE, Montevecchi WA, Andrews HF, Sims N (1988) Constraints on nest site selection: A comparison of predator and flood avoidance in four species of marsh-nesting birds (Genera: Catoptrophorus, Larus, Rallus, and Sterna). J Comparat Psychol 102:14–20

 

Tryjanowski P, Kuzniak S, Diehl B (2000) Does breeding performance of Redbacked Shrike Lanius collurio depend on nest site selection? Ornis Fennica 77:137–141

 

Watson M, Wilson JM, Koshkin M, Sherbakov B, Karpov F, Gavrilov A, Schielzeth H, Brombacher M, Collar NJ, Cresswell W (2006) Nest survival and productivity of the critically endangered Sociable Lapwing Vanellus gregarious. Ibis 148:489–502

 

Wiebe K, Martin K (1998) Costs and benefits of nest cover for ptarmigan: changes within and between years. Anim Behav 56:1137–1144

Avian Research
Article number: 5
Cite this article:
Dorge T, Högstedt G, Lislevand T. Nest distribution and nest habitat of the Tibetan Partridge (Perdix hodgsoniae) near Lhasa, Tibet. Avian Research, 2014, 5(1): 5. https://doi.org/10.1186/s40657-014-0005-7

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Received: 04 August 2014
Accepted: 08 August 2014
Published: 10 October 2014
© 2014 Dorge et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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