首页> 外文期刊>American journal of primatology >Sleeping Tree Selection of Cao Vit Gibbon (Nomascus nasutus) Living in Degraded Karst Forest in Bangliang, Jingxi, China
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Sleeping Tree Selection of Cao Vit Gibbon (Nomascus nasutus) Living in Degraded Karst Forest in Bangliang, Jingxi, China

机译:生活在靖西邦良退化喀斯特森林中的长臂猿(Nomascus nasutus)的睡树选择

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We studied the sleep-related behavior of two Cao Vit gibbon (Nomascus nasutus) groups in Bangliang Nature Reserve in Jingxi County, China between January 2008 and December 2009 to test four hypotheses related to sleeping tree selection (predation avoidance, thermoregulation, food access, and range defense). Gibbons entered sleeping trees 88 ± SD 37 min before sunset before their main potential nocturnal predator become active. They usually moved rapidly and straight to sleeping trees and kept silent once settled. Over the course of the study, gibbon groups used many (87 and 57 per group) sleeping trees and reused them irregularly. They also tended to sleep in relatively tall trees without lianas, choosing small branches close to the treetop. These behaviors would make it difficult for potential terrestrial predators to detect and approach the gibbons. Therefore, these results strongly support the predation avoidance hypothesis. Gibbons tended to sleep closer to ridges than to valley bottoms and they did not sleep at lower elevations in colder months. They thus appeared not to select sleeping trees to minimize thermoregulatory stress. Gibbons very rarely slept in feeding trees, instead generally sleeping more than 100 m away from the last feeding trees of the day or the first feeding tree of the next morning. These patterns led us to reject the food access hypothesis. Lastly, we did not find evidence to support the range defense hypothesis because gibbons did not sleep in overlap areas with neighbors more often than expected based on the proportion of overlap and exclusively used areas
机译:我们研究了2008年1月至2009年12月之间在中国靖西县邦良自然保护区的两个Cao Vit长臂猿(Nomascus nasutus)群体与睡眠有关的行为,以检验与睡眠树选择相关的四个假设(避免捕食,温度调节,食物获取,和远程防御)。长臂猿在日落之前的88±SD 37分钟进入睡树,然后它们的主要潜在夜间掠食者开始活动。他们通常迅速而直接地走到沉睡的树木上,并在定居后保持沉默。在研究过程中,长臂猿小组使用了许多睡觉树(每组分别为87和57),并不定期地重复使用它们。他们还倾向于在没有藤本植物的较高树上睡觉,选择靠近树梢的小树枝。这些行为将使潜在的地面掠食者难以发现和接近长臂猿。因此,这些结果有力地支持了避免捕食假说。长臂猿倾向于在山脊附近睡觉,而不是在谷底附近睡觉,并且在较冷的月份中它们在较低的海拔高度上没有睡觉。因此,他们似乎没有选择沉睡的树木以最小化温度调节压力。长臂猿很少睡在饲喂树上,而是通常睡在距离当天最后的饲喂树或第二天早晨的第一棵饲喂树100多米远的地方。这些模式导致我们拒绝食物获取假说。最后,我们没有找到支持射程防御假设的证据,因为长臂猿没有在与邻国重叠的区域睡得比根据重叠和专用区域的比例所预期的要多

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