常见的蜥蜴微栖息地选择因性别、奇偶模式和颜色而异。

Hans Recknagel, William T Harvey, Megan Layton, Kathryn R Elmer
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摘要

背景:动物以各种方式选择和与环境互动,包括确保它们的生理机能处于最佳状态,有可能获得猎物,以及可以避免捕食者。选择的平衡往往是相互矛盾的,这取决于个人的生活史和状况。普通的蜥蜴(胎生蜥蜴)有产卵和生育的血统,并显示出各种各样的背部图案和颜色。颜色和繁殖模式如何影响景观上的栖息地选择决策尚不清楚。在这项研究中,我们首先测试了共同发生的雄性和雌性胎生和卵生普通蜥蜴在其微栖息地选择上是否存在差异。其次,我们测试了一只蜥蜴的背部颜色是否与它所遇到的微栖息地内的日光浴地点选择相匹配,这可能与伪装和隐蔽有关。结果:生境利用方式不同于其他生境,表明蜥蜴主动选择其微生境的组成和结构。与雄性相比,雌性出现在树木较多、裸露地面较少的地区;我们推测,这可能是为了更好地伪装,减少怀孕期间被捕食的风险,因为怀孕期间雌性的流动性较差。微生境的使用也因胎次模式而异:胎生蜥蜴在开花植物密度更高的地区被发现,而胎生蜥蜴在更潮湿、苔藓更多的地区被发现。这可能与胎生动物和卵生动物对产卵地点的不同栖息地偏好有关。我们发现一个个体的背部颜色与其晒地的基质颜色相匹配。这可能表明个体可能会选择他们的日光浴地点来优化微栖息地的伪装。此外,所有的个体都在靠近掩蔽物的地方晒太阳,我们认为这可以用来躲避捕食者。结论:我们的研究表明,普通蜥蜴可能会主动选择自己的微栖息地和晒地,平衡生理需求、逃跑反应和伪装作为躲避捕食者的策略。这因胎次模式、性别和背部颜色而异,表明个体优化策略受到种群内个体间变异的影响,并由与生活史相关的进化差异决定。
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Common lizard microhabitat selection varies by sex, parity mode, and colouration.

Background: Animals select and interact with their environment in various ways, including to ensure their physiology is at its optimal capacity, access to prey is possible, and predators can be avoided. Often conflicting, the balance of choices made may vary depending on an individual's life-history and condition. The common lizard (Zootoca vivipara) has egg-laying and live-bearing lineages and displays a variety of dorsal patterns and colouration. How colouration and reproductive mode affect habitat selection decisions on the landscape is not known. In this study, we first tested if co-occurring male and female viviparous and oviparous common lizards differ in their microhabitat selection. Second, we tested if the dorsal colouration of an individual lizard matched its basking site choice within the microhabitat where it was encountered, which could be related to camouflage and crypsis.

Results: We found that site use differed from the habitat otherwise available, suggesting lizards actively choose the composition and structure of their microhabitat. Females were found in areas with more wood and less bare ground compared to males; we speculate that this may be for better camouflage and reducing predation risk during pregnancy, when females are less mobile. Microhabitat use also differed by parity mode: viviparous lizards were found in areas with more density of flowering plants, while oviparous lizards were found in areas that were wetter and had more moss. This may relate to differing habitat preferences of viviparous vs. oviparous for clutch lay sites. We found that an individual's dorsal colouration matched that of the substrate of its basking site. This could indicate that individuals may choose their basking site to optimise camouflage within microhabitat. Further, all individuals were found basking in areas close to cover, which we expect could be used to escape predation.

Conclusions: Our study suggests that common lizards may actively choose their microhabitat and basking site, balancing physiological requirements, escape response and camouflage as a tactic for predator avoidance. This varies for parity modes, sexes, and dorsal colourations, suggesting that individual optimisation strategies are influenced by inter-individual variation within populations as well as determined by evolutionary differences associated with life history.

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