Ecomorphology of the Locomotor Apparatus in the Genus Cyrtodactylus (Gekkota, Squamata)

IF 1.9 2区 生物学 Q3 EVOLUTIONARY BIOLOGY
Jendrian Riedel, L. Lee Grismer, Timothy Higham, Joseph Wu, Quyen Hanh Do, Truong Quang Nguyen, Camila G. Meneses, Rafe M. Brown, Patrick D. Campbell, Thomas Ziegler, Anthony P. Russell, Dennis Rödder
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Abstract

Adaptive radiations garner considerable interest from evolutionary biologists. Lizard radiations diversifying along structural niche space often exhibit distinct changes in body and limb proportions. One prediction is that terrestrial species inhabiting open habitats will have relatively longer hindlimbs, associated with faster running speeds, while scansorial species will have relatively shorter limbs to keep the centre of mass closer to the substratum. Alternatively, terrestrial species in densely vegetated habitats could benefit from relatively shorter limbs to prevent entanglement with more frequently encountered obstacles, whereas scansorial species could benefit from longer limbs promoting greater limb spans and static stability. Cyrtodactylus, an ecologically diverse gekkonid genus, includes numerous specialists with narrow structural niches, but the degree of morphological diversification exhibited by these specialists is largely unknown. We investigated associations between locomotor morphology and structural microhabitat use in Cyrtodactylus to test if either of the opposing predictions can be corroborated for this radiation. We measured body length and relative limb dimensions of 87 species, covering multiple independent transitions among structural microhabitat preferences. Using these data, we reconstructed the phylomorphospace and tested for associations between structural microhabitat niche and limb morphology. We found strong separation between structural niche groups in accordance with the second hypothesis, although overlap is evident among functionally related niches such as those of granite and karst specialists.

Abstract Image

Cyrtodactylus属(Gekkota,有鳞类)运动器械的形态学研究
适应性辐射引起了进化生物学家的极大兴趣。沿着结构生态位空间进行多样性演化的蜥蜴种群通常会在身体和肢体比例上表现出明显的变化。一种预测是,栖息在开阔生境中的陆生物种后肢相对较长,与较快的奔跑速度有关,而攀缘物种的四肢相对较短,以保持质量中心更靠近底层。另外,植被茂密的栖息地中的陆生物种可能会从相对较短的肢体中获益,以防止与更常遇到的障碍物缠绕,而有鳞物种可能会从较长的肢体中获益,以促进更大的肢展和静态稳定性。Cyrtodactylus是一种生态多样性的壁虎属动物,包括许多具有狭窄结构壁龛的专科动物,但这些专科动物所表现出的形态多样化程度在很大程度上是未知的。我们研究了Cyrtodactylus的运动形态与结构性微生境利用之间的关联,以检验是否可以证实该辐射中的任何一种相反预测。我们测量了 87 个物种的体长和相对肢体尺寸,涵盖了结构性微生境偏好的多个独立过渡。利用这些数据,我们重建了系统形态空间,并检验了结构性微生境生态位与肢体形态之间的关联。我们发现,尽管花岗岩和岩溶专家等功能相关的生态位之间存在明显的重叠,但根据第二个假说,结构生态位群体之间存在明显的分离。
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来源期刊
Evolutionary Biology
Evolutionary Biology 生物-进化生物学
CiteScore
3.80
自引率
4.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: The aim, scope, and format of Evolutionary Biology will be based on the following principles: Evolutionary Biology will publish original articles and reviews that address issues and subjects of core concern in evolutionary biology. All papers must make original contributions to our understanding of the evolutionary process. The journal will remain true to the original intent of the original series to provide a place for broad syntheses in evolutionary biology. Articles will contribute to this goal by defining the direction of current and future research and by building conceptual links between disciplines. In articles presenting an empirical analysis, the results of these analyses must be integrated within a broader evolutionary framework. Authors are encouraged to submit papers presenting novel conceptual frameworks or major challenges to accepted ideas. While brevity is encouraged, there is no formal restriction on length for major articles. The journal aims to keep the time between original submission and appearance online to within four months and will encourage authors to revise rapidly once a paper has been submitted and deemed acceptable.
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