四种利用不同生境蜥蜴运动能力的形态特征相关性

动物体态特征、功能表现和生境利用之间是否存在相关性是当前生态形态学领域的一个研究焦点。在实验室条件下测定分别利用开阔地面、草丛、岩石、树丛生境的 4种蜥蜴 (中国石龙子、北草蜥、山地麻蜥和变色树蜥 )的形态特征和运动能力 ,着重探讨蜥蜴运动能力与形态特征之间的相关性。 4种蜥蜴的头体长大小依次为 :中国石龙子 >变色树蜥 >北草蜥 >山地麻蜥。就相对体长而言 ,中国石龙子 >山地麻蜥和北草蜥 >变色树蜥 ,而头大小、附肢长度和尾长的种间差异趋势则相反 ;体高的种间差异为北草蜥 >中国石龙子和变色树蜥 >山地麻蜥。在平面上 ,山地麻蜥和北草蜥的速度显著大于中国石龙子和变色树蜥 ;在斜面上 ,变色树蜥和山地麻蜥的速度显著高于中国石龙子。变色树蜥斜面附着能力最强 ,中国石龙子最弱。生境利用不同的蜥蜴形态迥异 ,运动能力亦因此有显著的差异。本研究结果支持动物形态特征与其功能表现相关的观点。     

不同基质对北草蜥和中国石龙子运动表现的影响

动物在野外生境中的活动能力通常会受到许多方面(例如,运动基质表面粗糙程度、遭遇障碍物的大小与形状)的影响。在特定体温(30 ℃)条件下,测量主要分布区重叠的两蜥蜴种类(北草蜥和中国石龙子)在四种不同基质表面(塑料草坪;表面粗糙不透底的塑料地毯;光滑具透底网格的塑料地毯和表面光滑的塑料地毯)的运动表现,以及两者的攀附能力和最大游泳耐力。基质类型显著影响两种蜥蜴的运动表现。两种蜥蜴在粗糙表面运动时的疾跑速明显大于光滑表面(例如,塑料草坪上北草蜥为15.7 SVL/s,中国石龙子为8.1 SVL/s;光滑塑料地毯上则分别为11.4 SVL/s和3.5 SVL/s)。中国石龙子在光滑塑料地毯上具有最大的持续运动距离(10.6 SVL)和最少的停顿次数(1.9次)。北草蜥在光滑塑料地毯上具有最多的停顿次数(4.6次)。两种蜥蜴运动能力的种间差异显著。北草蜥具有较大的相对疾跑速度(北草蜥和中国石龙子:13.5 SVL/s vs 5.8 SVL/s)和攀附能力(143.8 ° vs 101.2 °),但较小的游泳耐力(83.5 s vs 238.5 s)。运动速度与耐力之间存在种间权衡关系而与攀爬能力无进化冲突的结论。     

断尾对蓝尾石龙子能量储存和运动表现的影响

在许多蜥蜴种类中,尾自切是一种主要的逃避天敌捕食的防御性策略。虽然断尾使蜥蜴获得短期的生存利益,但同时也需为此承受多方面的代价。利用从丽水采集的117条蓝尾石龙子来评价该种动物断尾的能量和运动代价。81条(约69%)石龙子至少经历过1次尾自切。断尾个体中,原先断尾事件的发生频率在不同尾区间存在显著差别,但两性间无差别。将实验组17条具完整尾的石龙子依次切去3个尾段,然后测定断尾前后石龙子的运动表现以及每个尾段、身体各部分中的脂肪含量。另15条具完整尾的石龙子作为对照组,仅测量其运动表现。尾部的脂肪含量与尾基部宽呈正相关,说明具较粗尾部的石龙子一般具有相当较多的尾部储能。尾部脂肪含量随尾长呈非等比例分布,大部分脂肪集中于尾近基部端。断尾几乎不影响蓝尾石龙子的运动表现,仅当大部分尾部被切除时疾跑速有较小程度的降低。显示了蓝尾石龙子因遭遇天敌捕食攻击或其它因素作用而产生的部分断尾可能并不会导致严重的能量和运动代价。由于野外种群蓝尾石龙子个体的断尾情况主要发生在尾近基部或中部位置,因此可以认为自然条件下该种动物的尾自切通常会遭受明显的能量和运动代价。     

爬行动物常用的生态学研究及实验技术简介

对爬行动物进行野外生态科研调查及实验研究时 ,经常会应用如下几种技术 :1　鉴别雌雄野外活捉动物后 ,不管是留活体饲养 ,还是做成标本 ,都要鉴定其雌雄性别 ,鉴定的方法有 :1 )外部鉴别特征 :爬行动物中的蜥蜴类动物生活时雌性个体与雄性个体的体色相差比较大 ,尤其在生殖季节这种差别更明显 ,如 :中国石龙子雄体体侧红棕色斑纹比雌体鲜艳醒目 ;变色树蜥雄蜥头颈肩部、生活时整个背面全为鲜红色 ,颈、颞、喉部散有黑斑 ,雌蜥没有那么明显的体色 ,南草蜥雄性背面有两条边缘齐整的窄绿纵纹 ,从头背侧至尾前部 ,雌体没有。此外 ,从蜥蜴头宽也…     

江西武功山两栖爬行动物资源调查及评价

2001年7月中旬～8月上旬,对江西武功山国家森林公园进行了20多天的野生动植物资源野外考察.公园内现已记录两栖类2目7科25种和爬行类3目9科37种,本次调查增加安福县爬行动物新记录7种：多疣壁虎、中国石龙子、黑背白环蛇、铅色水蛇、灰鼠蛇、乌梢蛇、银环蛇;增加武功山爬行动物新记录23种.动物地理区划属东洋界华中区东部丘陵平原亚区,动物区系组成以东洋界华中区与华南区共有种为主.两栖类东洋界种类占92.00%;生态类型以流水型9种和陆栖-静水型7种占优势.数量优势种为黑斑蛙、中华蟾蜍、黑斑肥螈、泽蛙、棘胸蛙、花臭蛙、华南湍蛙、三港树蟾、镇海林蛙和饰纹姬蛙.爬行类东洋界种类占75.68%,广布种占24.32%.数量优势种有石龙子、蓝尾石龙子、铜蜓蜥、赤链华游蛇、王锦蛇、虎斑颈槽蛇、赤链蛇、红点锦蛇、乌梢蛇、灰鼠蛇、尖吻蝮、竹叶青蛇等.公园内野生动物及其生境受人类干扰破坏大,当地群众保护意识有待增强,就此提出了保护对策.     

冬季清凉峰山区小麂和野猪的生境选择及差异

从2005 年11 月5 日至2006 年1 月21 日,为了评估小麂和野猪的生境选择及其差异,我们在浙江清凉峰国家级自然保护区核心区共设置了248 个样方群。研究发现,两者都选择平缓坡的灌丛植被、草本密度小、离住宅较近和离隐蔽物距离适中的生境,表现了它们的生境选择有一定的重叠性。但是它们也表现出生境选择的一些差异,小麂选择乔木密度适中、灌丛密度大和郁闭度适中的生境,而野猪选择乔木密度小的生境,随机地使用各类灌丛密度和郁闭度的生境。小麂还选择北坡、离水源距离较远的生境,野猪只是随机地使用不同的坡向和离水源距离的生境。分析两者共存的机制,我们发现小麂采取隐藏策略而野猪采取逃跑策略来避敌和利用资源,即它们之间存在与反捕食策略相关的生境选择差异。
     

斑块生境中食果鸟类对南方红豆杉种子的取食和传播

生境斑块化对食果鸟类的移动行为产生影响,进而影响其对植物种子的传播格局和效率。南方红豆杉(Taxus chinensis var.mairei)是我国一级保护植物,在南方山区多因人为干扰而呈斑块状分布。2011年,2012年10月底到12月中,以分布于福建梅花山国家级自然保护区红豆杉生态园中南方红豆杉种群为对象,研究斑块生境中鸟类对南方红豆杉种子的取食和传播行为,并评估专性鸟类和泛性鸟类的传播效率。结果发现:南方红豆杉源斑块共吸引22种食果鸟类取食红豆杉种子,并与13种鸟类形成了种子传播关系。不同年间,黑短脚鹎(Hypsipetes leucocephalus)都是植物的主要传播鸟类,而其他鸟类传播者种类具有一定的年间变化。生境斑块化导致专性鸟类黑短脚鹎和泛性鸟类红嘴蓝鹊(Urocissa erythrorhyncha)种子传播效率差异。与红嘴蓝鹊相比,黑短脚鹎飞行的平均距离较短((16.3±11.0)m,Mean±SD,n=125),传播距离相对较近;且它们取食后偏好在源斑块中活动,喜栖息在同种成树、甜楮(Castanopsis eyrei)及其他阔叶树等栖树上。红嘴蓝鹊取食后常在斑块间移动,常停歇在同种成树和毛竹(Phyllostachys heterocycla)上,传播距离相对较远((24.9±20.0)m,Mean±SD,n=95)。空间一致性结果表明,黑短脚鹎移动距离对幼苗更新距离的空间一致性程度高;而红嘴蓝鹊偏好生境与幼苗更新生境一致性程度高。结果表明,斑块生境中植物能与专性鸟类、泛性鸟类之间形成种子传播互惠关系,且种子传播效率受到专性鸟类和泛性鸟类传播距离和传播生境的影响。     

北戴河湿地朱鹮野化训练

朱鹮(Nipponia nippon)是世界濒危物种,中国Ⅰ级重点保护动物。为了进一步扩大其种群分布范围,2018年7月将20只朱鹮从陕西洋县朱鹮救护饲养中心引入到北戴河国家湿地公园开展野化饲养。为了解朱鹮对该地模拟自然环境的野化适应效果,于2018年7-10月对朱鹮在大网笼中的行为和栖息地利用进行了观察。野化训练过程中,朱鹮在训练笼中快速获得良好的飞行技巧,飞行中能够避免碰撞野化网笼软网。持续飞行时间从观察初期的(106.8±93.4)s,增长至后期的(145.8±118.1)s。野化训练第1天,有70%个体在树上夜宿,其他个体在地面及栖杠上夜宿;30 d时间内,朱鹮全部获得树上夜宿能力。野化训练后期和前期相比,觅食时间从55.4%提高至58.3%,并显著提高了对浅水觅食地的利用率。后期显著提高了警戒行为的时间比例,并表现出对猛禽等天敌的防御反应。通过87d的野化训练,试验个体的行为和生境利用发生较大变化并趋于稳定,表明其已基本适应了当地的新环境。为了进一步适应放飞后的野外环境多样性,建议在今后的野化训练中改变朱鹮的投食策略,增加觅食难度,并开展当地特有食物的投喂试验。     

新疆阜康地区家麻雀的巢址选择

2013年7月和2014年5~7月,在新疆阜康地区对家麻雀(Passer domesticus)的巢址选择进行调查,以分析影响家麻雀巢址选择的生态因子。在研究区内共找到75个家麻雀的自然巢,筑巢生境为农田和防护林带,均在白杨(Populus adenopoda)林和胡杨(P.euphratica)林中的树上筑巢。其中,繁殖成功巢40个,繁殖失败巢20个,15个巢未记录到繁殖结果。在研究区内的居民房屋、墙洞等没有发现家麻雀的巢。采用逻辑斯蒂回归和主成分分析方法对筑巢地海拔(m)、筑巢树种、筑巢树高(m)、巢距路距离(m)、巢距地面高度(m)、巢上方盖度(%)、筑巢树胸径(m)、最近邻巢的距离(m)这些家麻雀的主要巢址参数进行分析,结果表明,影响新疆阜康地区家麻雀巢址利用的主要因素为巢距地面高度(m)、巢上方盖度(%)和巢距路距离(m)。对家麻雀繁殖成功巢(n=40)和繁殖失败巢(n=20)的巢址参数进行比较,两者差异不显著,因而推测,在研究区域的尺度内,家麻雀的巢址选择并不是影响其繁殖成效的主要因素。     

四川雉鹑的冬季夜栖地选择

四川雉鹑(Tetraophasis szechenyii)是中国特有物种,国家Ⅰ级重点保护野生动物,对其冬季夜栖地选择的了解,有助于理解物种的生存策略,为物种保护提供参考。利用徒步跟踪和无线电遥测的方法,我们于2006年9月到2007年4月在四川省雅江县帕姆岭进行了野外研究。采用卡方检验、配对样本t检验和二元逻辑斯缔回归等方法对数据进行分析。结果发现:(1)四川雉鹑利用鳞皮冷杉(Abies squamata)和大果红杉(Larix potaninii var.macrocarpa)两种树夜栖,卡方检验分析发现四川雉鹑对这两树种没有明显的选择偏好(χ2=0.745,df=1,P=0.388);(2)夜栖树的胸径为(25.8±1.3)cm,夜栖枝条离地高度为(6.3±0.3)m,直径为(3.3±0.1)cm;(3)与对照样地相比,夜栖地生境一般靠近林缘,乔木的平均胸径大、林下盖度小、倒木数量多,夜栖树胸径大、最近乔木胸径大和最近乔木距离远;(4)逻辑斯缔回归分析表明:夜栖树第一枝距地面高为冬季四川雉鹑夜栖地选择的关键因子;倒木数量、平均乔木胸径、最近林缘距离为次关键因子,该模型对夜栖地的预测正确率为80.9%。冬季四川雉鹑选择夜栖地是安全、能量和地点转移三个因素综合作用的结果,在不同的环境下,同一物种对环境会有不同的适应策略。     

Escape tactics and effects of perch height and habituation on flight initiation distance in two Jamaican anoles (Squamata: polychrotidae)

Escape by Anolis lizards is influenced by microhabitats and fight initiation distance increases with predation risk. Differences in microhabitat use among ecomorphs affect escape behavior, but only two studies have reported ecomorphological differences in flight initiation distance among Greater Antillean species. I studied effects of predation risk and microhabitats on escape behavior by conducting field experiments using two species of anoles, Anolis lineatopus and A. grahami, on the campus of the University of the West Indies at Mona, Jamaica. Because ecomorphological variation of anoles has evolved independently within each island of the Greater Antilles, but relationships between ecomorphs and escape behaviors are poorly known, I characterized microhabitat use and escape tactics, and determined relationships between flight initiation distance and two risk factors, habituation to human presence and perch height, in Anolis lineatopus, a trunk-ground anole and A. grahami, a trunk-crown anole. Sample sizes for A. lineatopus and A. grahami were 214 and 93, for microhabitat use and escape destinations, 74 and 34 for human presence and 125 and 34 for perch height. The two species occurred in similar microhabitats and exhibited similar escape tactics, but exhibited key differences expected for their ecomorphs. Both species were sighted frequently on the ground and on trees, but A. lineatopus were more frequently on ground and were perched lower than A. grahami. Both species escaped from ground to trees and when on trees hid on far sides and escaped without changing climbing direction with equal frequency. The frequency of fleeing upward was greater for A. grahami than A. lineatopus. Both species exhibited habituation by having shorter flight initiation distances in areas with more frequent exposure to people. In both species flight initiation distance increased as perch height decreased because, lizards had to climb farther to be out of reach when perched lower. The relationship between flight initiation distance and perch height may apply to other anole ecomorphs that flee upward when low perched on trees.     

Optimal escape theory predicts escape behaviors beyond flight initiation distance： risk assessment and escape by striped plateau lizards Sceloporus virgatus

Escape theory predicts that flight initiation distance (FID=distance between predator and prey when escape begins) is longer when risk is greater and shorter when escape is more costly. A few tests suggest that escape theory applies to distance fled. Escape models have not addressed stochastic variables, such as probability of fleeing and of entering refuge, but their economic logic might be applicable. Experiments on several risk factors in the lizard Sceloporus virgatus confirmed all predictions for the above escape variables. FID was greater when approach was faster and more direct, for lizards on ground than on trees, for lizards rarely exposed to humans, for the second of two approaches, and when the predator turned toward lizards rather than away. Lizards fled further during rapid and second consecutive approaches. They were more likely to flee when approached directly, when a predator turned toward them, and during second approaches. They were more likely to enter refuge when approached rapidly. A novel finding is that perch height in trees was unrelated to FID because lizards escaped by moving out of sight, then moving up or down unpredictably. These findings add to a growing body of evidence supporting predictions of escape theory for FID and distance fled. They show that two probabilistic aspects of escape are predictable based on relative predation risk levels. Because individuals differ in boldness, the assessed optimal FID and threshold risks for fleeing and entering refuge are exceeded for an increasing proportion of individuals as risk increases[Current Zoology 55(2):123-131,2009].     

Universal Optimization of Flight Initiation Distance and Habitat-Driven Variation in Escape Tactics in a Namibian Lizard Assemblage

Some aspects of escape predicted by theoretical models are intended to apply universally. For example, flight initiation distance (distance between an approaching predator and prey when escape begins) is predicted from predation risk and the costs of escaping. Escape tactics and refuge selection are not currently predicted by theoretical models, but are expected to vary with structural features of the habitat. One way of studying such variation is to compare aspects of antipredatory behavior among sympatric species that differ in habitat or microhabitat use. In an assemblage of lizards in northwestern Namibia, we conducted experiments to test predictions of escape theory for three risk factors in representatives of three families and observed escape tactics in additional species. As predicted by escape theory, flight initiation distance increased with directness of a predator's approach and predator speed in Agama planiceps, Mabuya acutilabris, and Rhotropus boultoni, and with distance from refuge in M. acutilabris. As predicted by theory, the probability of entering refuge increased with risk in R. boultoni. All available data indicate that flight initiation distance and refuge entry by lizards conform to theoretical predictions. Escape tactics varied greatly as a function of habitat type: (1) arboreal species fled up and around trees and sometimes entered tree holes; (2) saxicolous species used rock crevices as refuges, but differed in tactics prior to entering refuges; and (3) terrestrial species fled into bushes or other vegetation, often to the far sides of them. Some M. acutilabris entered small animal burrows or buried themselves in sand beneath bushes. Escape tactics varied even among congeners in Mabuya, highlighting the important effect of habitat structure on them. Although habitat partitioning has traditionally been viewed as favoring species coexistence, an interesting by‐product appears to be structuring of escape tactics in lizard communities.     

Costs of Refuge Use Affect Escape Decisions of Iberian Rock Lizards Lacerta monticola

Theoretical models of anti-predator escape behaviour suggest that prey may adjust their escape response such that the optimal flight distance is the point at which the costs of staying exceed the costs of fleeing. Anti-predatory decisions should be made based also on consequences for long-term expected fitness, such as the costs of refuge use. For example, in lizards, the maintenance of an optimal body temperature is essential to maximize physiological processes. However, if unfavourable thermal conditions of refuges can decrease the body temperature of lizards, their escape decision should be influenced by refuge conditions. Analyses of the variation in flight distances and emergence latency from a refuge for the lizard Lacerta monticola under two different predation risk levels, and their relationship with the thermal environment, supported these predictions. When risk increased, lizards had longer emergence latencies, and thus costs of refuge use increased (a greater loss of time and body temperature). In the low-risk situation, lizards that were farther from the refuge had longer flight distances, whereas thermal conditions were less important. When risk increased, lizards had longer flight distances when refuges were farther off, but also when the external heating rate and the refuge cooling rate were lower. The results suggest that, in addition to the risk of predation, expected long-term fitness costs of refuges can also affect escape decisions.     

Influence of Some Potential Predation Risk Factors and Interaction between Predation Risk and Cost of Fleeing on Escape by the Lizard Sceloporus virgatus

Escape theory predicts that flight initiation distance (predator–prey distance when escape begins) increases as predation risk increases and decreases as cost of fleeing increases. Scant information is available about the effects of some putative predation risk factors and about interaction between simultaneously operating risk and cost of fleeing factors on flight initiation distance and distance fled. By simulating an approaching predator, I studied the effects of body temperature (BT), distance to nearest refuge, and eye contact with a predator, as well as simultaneous effects of predator approach speed and female presence/absence on escape behavior by a small ectothermic vertebrate, the lizard Sceloporus virgatus. Flight initiation distance decreased as BT increased, presumably because running speed increases as BT increases, facilitating escape. Distance to nearest refuge was unrelated to BT or flight initiation distance. Substrate temperature was only marginally related, and air temperature was not related to flight initiation distance. Eye contact did not affect flight initiation during indirect approaches that bypassed lizards by a minimum of 1 m, but an effect of eye contact found in other studies during direct approach might occur. Predator approach speed and presence of a female interactively affected flight initiation distance, which increased as speed increased and decreased when a female was present. In the presence of a female, flight initiation distance was far shorter than when no female was present. The high cost of forgoing a mating opportunity accounts for the interaction because the difference between female presence and absence is greater when risk is greater.     

At home with the birds: Kalahari tree skinks associate with sociable weaver nests despite African pygmy falcon presence

The way in which animals use habitat can affect their access to key resources or how they are buffered from environmental variables such as the extreme temperatures of deserts. One strategy of animals is to modify the environment or take advantage of structures constructed by other species. The sociable weaver bird (Philetairus socius) constructs enormous colonial nests in trees. These nests are frequented by Kalahari tree skinks (Trachylepis spilogaster) and the two species coexist over a large portion of the Kalahari Desert in South Africa. We tested whether skinks were more abundant in trees containing sociable weaver nests and asked whether the physical features of trees were important predictors of skink abundance. We then focused on potential costs of this association by examining the relationship between skink abundance and the presence of a potential predator, the pygmy falcon (Polihierax semitorquatus), which exclusively uses weaver nest colonies for roosting and nesting. Finally, we simulated a predatory threat to determine if skinks assess risk differently if a weaver nest is present. We found a significant positive association between the presence of weaver nests and skink abundance. In the absence of nests, the type of tree did not influence skink abundance. Skinks used weaver nests and were more likely to perch on the nest than the tree. When threatened with predation, skinks preferred to take refuge in nests. Surprisingly, the presence of nesting pygmy falcons in nests did not influence skink abundance, perhaps because of the abundance of nearby refuges within nests, tree crevices, or in debris at the tree base. We suggest that sociable weaver nests provide multiple benefits to skinks including lowered predation risk, thermal refuges and greater prey availability, although this requires experimental testing. In the current era of global climate change, sociable weaver nests may become a crucial resource for skinks seeking refuge as the Kalahari climate warms.     

Predation Risk and Opportunity Cost of Fleeing While Foraging on Plants Influence Escape Decisions of an Insular Lizard

Cost‐benefit models of escape behaviour predict how close a prey allows a predator to approach [flight initiation distance (FID)] based on cost of not fleeing (predation risk) and cost of fleeing (loss of opportunities). Models for FID have been used with some success to predict distance fled (DF). We studied effects of foraging opportunity cost of fleeing and examined differences between age‐sex groups in the omnivorous Balearic Lizard, Podarcis lilfordi. Balearic lizards forage on the ground for invertebrate prey and climb the thistle Carlina corymbosa to forage on its inflorescences. We studied escape behaviour in three experimental groups, with human beings as simulated predators: lizard foraging above ground on C. corymbosa, foraging on the ground away from thistles and on the ground with cut inflorescences. Flight initiation distance was shorter for lizards with cut inflorescences than for (1) lizards above ground due to the greater risk above ground due to conspicuousness of black lizards on yellow flowers; and (2) lizards on ground away from flowers due to the cost of leaving while feeding. The only age‐sex difference was slightly greater FID for adult males than subadults, presumably because larger adult males are more likely to be attacked by predators. Other potential factors affecting this difference are discussed. Experimental group and age‐sex group did not interact for FID or DF. Because lizards foraging on inflorescences above ground fled to the base of the plants to refuge provided by spiny thistle leaves, their DF was shorter than in the other groups, which fled across the ground, usually without entering refuge. DF did not differ between groups on the ground or among age‐sex groups. The predicted shorter DF for lizards with cut inflorescences than on ground without inflorescences did not occur. We hypothesize that the opportunity cost was small due to the abundance of blooming thistles and that DF may be less sensitive to opportunity cost than FID.     

Plesiomorphic Escape Decisions in Cryptic Horned Lizards (Phrynosoma) Having Highly Derived Antipredatory Defenses

Escape theory predicts that the probability of fleeing and flight initiation distance (predator–prey distance when escape begins) increase as predation risk increases and decrease as escape cost increases. These factors may apply even to highly cryptic species that sometimes must flee. Horned lizards (Phrynosoma) rely on crypsis because of coloration, flattened body form, and lateral fringe scales that reduce detectability. At close range they sometimes squirt blood‐containing noxious substances and defend themselves with cranial spines. These antipredatory traits are highly derived, but little is known about the escape behavior of horned lizards. Of particular interest is whether their escape decisions bear the same relationships to predation risk and opportunity costs of escaping as in typical prey lacking such derived defenses. We investigated the effects of repeated attack and direction of predator turning on P. cornutum and of opportunity cost of fleeing during a social encounter in P. modestum. Flight initiation distance was greater for the second of two successive approaches and probability of fleeing decreased as distance between the turning predator and prey increased, but was greater when the predator turned toward than away from a lizard. Flight initiation distance was shorter during social encounters than when lizards were solitary. For all variables studied, risk assessment by horned lizards conforms to the predictions of escape theory and is similar to that in other prey despite their specialized defenses. Our findings show that these specialized, derived defenses coexist with a taxonomically widespread, plesiomorphic method of making escape decisions. They suggest that escape theory based on costs and benefits, as intended, applies very generally, even to highly cryptic prey that have specialized defense mechanisms.     

The ontogeny of escape behavior,locomotor performance,and the hind limb in Sceloporus woodi

Flight initiation distance describes the distance at which an animal flees during the approach of a predator. This distance presumably reflects the tradeoff between the benefits of fleeing versus the benefits of remaining stationary. Throughout ontogeny, the costs and benefits of flight may change substantially due to growth-related changes in sprint speed; thus ontogenetic variation in flight initiation distance may be substantial. If escape velocity is essential for surviving predator encounters, then juveniles should either tolerate short flight initiation distances and rely on crypsis, or should have high flight initiation distances to remain far away from their predators. We examined this hypothesis in a small, short-lived lizard (Sceloporus woodi). Flight initiation distance and escape velocity were recorded on an ontogenetic series of lizards in the field. Maximal running velocity was also quantified in a laboratory raceway to establish if escape velocities in the field compared with maximal velocities as measured in the lab. Finally a subset of individuals was used to quantify how muscle and limb size scale with body size throughout ontogeny. Flight initiation distance increased with body size; larger animals had higher flight initiation distances. Small lizards had short flight initiation distances and remained immobile longer, thus relying on crypsis for concealment. Escape velocity in the field did not vary with body size, yet maximum velocity in the lab did increase with size. Hind limb morphology scaled isometrically with body size. Isometric scaling of the hind limb elements and its musculature, coupled with similarities in sprint and escape velocity across ontogeny, demonstrate that smaller S. woodi must rely on crypsis to avoid predator encounters, whereas adults alter their behavior via larger flight initiation distance and lower (presumably less expensive) escape velocities.     

Choosing among alternative refuges: Distances and directions

Many prey flee to refuges to escape from approaching predators, but little is known about how they select one among many refuges available. The problem of choice among alternative refuges has not been modeled previously, but a recent model that predicts flight initiation distance (FID = predator–prey distance when escape starts) for a prey fleeing to a refuge provides a basis for predicting which refuge should be chosen. Because fleeing is costly, prey should choose to flee to the refuge permitting the shortest FID. The model predicts that the more distant of two refuges can be favored if it is not too far and if the prey's trajectory to the farther refuge is more away from the predator than the direction to the nearer refuge. The difference in predicted FID between the farther and nearer refuges increases curvilinearly as the interpath angle for the farther refuge increases. The difference in predicted FID between the farther and nearer refuges increases linearly as the distance to the farther refuge increases. An isocline describing where nearer and farther refuges are equally favored shows a negative curvilinear relationship between interpath angle and prey distance to the farther refuge. In the region below the isocline, the farther refuge is favored, whereas above the isocline the prey should flee to the nearer refuge.