When the Going Gets Tough, the Females Get Going: Sex-Specific Physiological Responses to Simultaneous Exposure to Hypoxia and Marine Heatwave Events in a Ubiquitous Copepod

IF 10.8 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Global Change Biology Pub Date : 2024-10-25 DOI:10.1111/gcb.17553
Fanny Vermandele, Matthew Sasaki, Gesche Winkler, Hans G. Dam, Diana Madeira, Piero Calosi
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Abstract

The existence of sex-specific differences in phenotypic traits is widely recognized. Yet they are often ignored in studies looking at the impact of global changes on marine organisms, particularly within the context of combined drivers that are known to elicit complex interactions. We tested sex-specific physiological responses of the cosmopolitan and ecologically important marine copepod Acartia tonsa exposed to combined hypoxia and marine heatwave (MHW) conditions, both of which individually strongly affect marine ectotherms. Females and males were acutely exposed for 5 days to a combination of either control (18°C) or a high temperature mimicking a MHW (25°C), and normoxia (100% O2 sat.) or mild hypoxia (35% O2 sat.). Life-history traits, as well as sex-specific survival and physiological traits, were measured. Females had overall higher thermal tolerance levels and responded differently than males when exposed to the combined global change drivers investigated. Females also showed lower metabolic thermal sensitivity when compared to males. Additionally, the MHW exerted a dominant effect on the traits investigated, causing a lower survival and higher metabolic rate at 25°C. However, egg production rates appeared unaffected by hypoxia and MHW conditions. Our results showed that MHWs could strongly affect copepods' survival, that combined exposure to hypoxia and MHW exerted an interactive effect only on CTmax, and that sex-specific vulnerability to these global change drivers could have major implications for population dynamics. Our results highlight the importance of considering the differences in the responses of females and males to rapid environmental changes to improve the implementation of climate-smart conservation approaches.

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艰难困苦,玉汝于成:无处不在的桡足类对同时暴露于缺氧和海洋热浪事件的性别特异性生理反应
表型特征中存在性别差异已被广泛认可。然而,在研究全球变化对海洋生物的影响时,它们往往被忽视,尤其是在已知会引起复杂相互作用的综合驱动因素的背景下。我们测试了在缺氧和海洋热浪(MHW)条件下,具有世界性和生态重要性的海洋桡足类扁形目(Acartia tonsa)的性别特异性生理反应。雌性和雄性急性暴露于对照组(18°C)或模拟海洋热浪的高温(25°C)、常氧(100%氧气饱和度)或轻度缺氧(35%氧气饱和度)的组合条件下5天。对生命史特征以及性别特异性生存和生理特征进行了测量。与雄性相比,雌性的热耐受水平总体较高,但在暴露于所研究的综合全球变化驱动因素时,雌性的反应却与雄性不同。与雄性相比,雌性的新陈代谢热敏感性也较低。此外,MHW对所调查的性状产生了主导影响,导致雌性在25°C时存活率较低,新陈代谢率较高。然而,产卵率似乎不受缺氧和MHW条件的影响。我们的研究结果表明,MHW会强烈影响桡足类的存活率,同时暴露于缺氧和MHW条件下只会对CTmax产生交互影响,而且不同性别对这些全球变化驱动因素的脆弱性会对种群动态产生重大影响。我们的研究结果突显了考虑雌性和雄性对快速环境变化的反应差异对改进气候智能保护方法的实施的重要性。
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来源期刊
Global Change Biology
Global Change Biology 环境科学-环境科学
CiteScore
21.50
自引率
5.20%
发文量
497
审稿时长
3.3 months
期刊介绍: Global Change Biology is an environmental change journal committed to shaping the future and addressing the world's most pressing challenges, including sustainability, climate change, environmental protection, food and water safety, and global health. Dedicated to fostering a profound understanding of the impacts of global change on biological systems and offering innovative solutions, the journal publishes a diverse range of content, including primary research articles, technical advances, research reviews, reports, opinions, perspectives, commentaries, and letters. Starting with the 2024 volume, Global Change Biology will transition to an online-only format, enhancing accessibility and contributing to the evolution of scholarly communication.
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