Tadpoles Develop Elevated Heat Tolerance in Urban Heat Islands Regardless of Sex

IF 1.9 2区 生物学 Q3 EVOLUTIONARY BIOLOGY
Veronika Bókony, Emese Balogh, János Ujszegi, Nikolett Ujhegyi, Márk Szederkényi, Attila Hettyey
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Abstract

The ability of wildlife to endure the effects of high temperatures is increasingly important for biodiversity conservation under climate change and spreading urbanization. Organisms living in urban heat islands can have elevated heat tolerance via phenotypic or transgenerational plasticity or microevolution. However, the prevalence and mechanisms of such thermal adaptations are barely known in aquatic organisms. Furthermore, males and females can differ in heat tolerance, which may lead to sex-biased mortality, yet it is unknown how sex differences in thermal biology influence urban phenotypic divergence. To address these knowledge gaps, we measured critical thermal maxima (CTmax) in male and female agile frog (Rana dalmatina) tadpoles captured from warm urban ponds and cool woodland ponds, and in a common-garden experiment where embryos collected from both habitat types were raised in the laboratory. We found higher CTmax in urban-dwelling tadpoles compared to their counterparts living in woodland ponds. This difference was reversed in the common-garden experiment: tadpoles originating from urban ponds had lower CTmax than tadpoles originating from woodland ponds. We found no effect of sex on CTmax or its difference between habitats. These results demonstrate that aquatic amphibian larvae can respond to the urban heat island effect with increased heat tolerance similarly to other, mostly terrestrial taxa studied so far, and that phenotypic plasticity may be the main driver of this response. Our findings also suggest that heat-induced mortality may be independent of sex in tadpoles, but research is needed in many more taxa to explore potentially sex-dependent urban thermal responses.

Abstract Image

城市热岛中的蝌蚪无论性别都会产生较强的耐热性
在气候变化和城市化不断扩大的情况下,野生动物承受高温影响的能力对于保护生物多样性越来越重要。生活在城市热岛中的生物可通过表型或跨代可塑性或微进化提高耐热性。然而,这种热适应性在水生生物中的普遍性和机制却鲜为人知。此外,雌性和雄性在耐热性上可能存在差异,这可能会导致有性别偏见的死亡率,但热生物学中的性别差异如何影响城市表型差异,目前还不得而知。为了填补这些知识空白,我们测量了从温暖的城市池塘和凉爽的林地池塘捕获的雄性和雌性敏捷蛙(Rana dalmatina)蝌蚪的临界最大热量(CTmax)。我们发现,与生活在林地池塘中的蝌蚪相比,生活在城市中的蝌蚪CTmax更高。这种差异在共同花园实验中得到了逆转:来自城市池塘的蝌蚪的 CTmax 低于来自林地池塘的蝌蚪。我们没有发现性别对CTmax的影响或生境间的差异。这些结果表明,水生两栖类幼体可以对城市热岛效应做出反应,提高耐热性,这与迄今为止研究的其他类群(主要是陆生类群)类似,表型可塑性可能是这种反应的主要驱动力。我们的研究结果还表明,热引起的死亡可能与蝌蚪的性别无关,但还需要对更多分类群进行研究,以探索可能与性别相关的城市热反应。
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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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