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61.
The habitat selection of Tibetan Snow Cocks in shrub vegetation was investigated in Lhasa,Tibet,China,between March and April,2005.Fourteen parameters were measured.These include altitude,slope,slope aspect,slope position,vegetation cover,plant type and other environmental parameters.Results show that Snow Cocks favor foraging in areas where vegetation cover was small and close to the residents' houses.Supplementary food supplied by humans has caused Snow Cocks to decrease their foraging range.Snow Cocks also favor roosting in areas with low vegetation,sparse grass,short grass,large rocks and close to houses.The Snow Cocks' activity in the study areas show a close relationship with human activities.  相似文献   
62.
Frequent references are made to presumed antipredator adaptations exhibited by callitrichids, but there are very few systematic investigations of these behaviors. One set of untested presumptions stems from observations that callitrichids become especially vigilant and cryptic prior to retirement each evening. This hypothesis was tested in the current study by quantifying the rates of vocalizations and extragroup behavior at various times of the day. Using two groups of captive red-bellied tamarins, it was demonstrated that these primates do become relatively more quiet and more attentive to the nonsocial environment prior to retirement each evening, culminating in virtual silence once the nest box has been entered. While the adaptive significance of these phenomena has not yet been tested, it is likely that the behaviors reduce vulnerability to predation.  相似文献   
63.
Grass Wrens Cistothorus platensis build two types of non-breeding nest structures: platforms and dummy nests. Platforms are rudimentary accumulations of grasses concealed between vegetation. Dummy and breeding nests are dome-shaped with a similar structural layer. We used a nest-removal experiment and observational data to evaluate several hypotheses regarding the adaptive significance of building multiple nests in a south temperate population of Grass Wrens. Building non-breeding nests was not a strategy of males to attract additional females, as most of these nests were built after pair formation and both sexes collaborated during building. Building non-breeding nests was not a post-pairing display as the presence of multiple nests did not increase female investment in the breeding attempt: clutch size and female provisioning to nestlings did not differ between experimental and control territories where no non-breeding nests were removed. Similarly, in non-manipulated territories, clutch size and female provisioning were not correlated with the number of non-breeding nests or with males’ nest-building effort. Contrary to this hypothesis, the number of non-breeding nests was associated with delayed clutch initiation and reduced hatching success. The presence of non-breeding nests did not reduce nest predation and brood parasitism, which did not differ between experimental and control territories. We did not detect differences in concealment between non-breeding and breeding nests, suggesting that non-breeding nests were not the result of abandonment before egg-laying to reduce subsequent nest predation. Dummy nests did not provide shelter; they were not used frequently for roosting over the breeding season and were not maintained during the non-breeding season. We suggest that building non-breeding nests may be an attempt by males to manipulate the decision of females to breed with a mate they might otherwise reject or to start reproduction earlier than optimal for the females.  相似文献   
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