在种群内部,对热和营养综合压力的可塑性反应不同于对单一压力的反应,而且在雄性和雌性的不同性状中具有遗传独立性。

IF 2.1 3区 生物学 Q3 ECOLOGY Journal of Evolutionary Biology Pub Date : 2024-05-17 DOI:10.1093/jeb/voae061
Yeuk Man Movis Choy, Greg M Walter, Christen K Mirth, Carla M Sgrò
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引用次数: 0

摘要

表型可塑性有助于动物缓冲气候变化造成的日益严重的热和营养压力的影响。不同基因的种群对单一和综合压力的可塑性反应会有所不同。然而,人们对一个种群中不同个体对综合压力的可塑性反应如何变化,以及这种变化是否会因生命史特征的不同而改变知之甚少。这一点非常重要,因为种群内的个体差异会影响种群对环境变化的反应。在这里,我们利用黑腹果蝇的同源系来评估卵到成虫的存活率和性别特异性体型在两种温度(25°C 或 28°C)和三种饮食(标准饮食、低热量饮食或低蛋白质:碳水化合物比例饮食)组合下的可塑性。我们的研究结果表明,卵到成虫的存活率和翅膀大小对热营养胁迫的可塑性在种群内存在巨大的遗传变异。这种可塑性的遗传变异是跨环境遗传相关性的结果,这两个性状的跨环境遗传相关性往往小于1,而且卵到成虫存活率的遗传变异在不同环境中的表达也发生了变化。当雌雄个体在不同条件下饲养时,体型的跨性别遗传相关性较弱,这表明性状的遗传基础可能会随着环境的变化而变化。此外,我们的研究结果表明,卵到成体存活率的可塑性在遗传上独立于体型的可塑性。重要的是,对食物和温度单独反应的可塑性与对食物和温度组合反应的可塑性转变不同。通过量化可塑性和遗传变异对不同性状综合压力的响应,我们的研究揭示了动物对环境变化响应的复杂性,以及对种群适应当前气候变化的潜力进行更细致理解的必要性。
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Within population plastic responses to combined thermal-nutritional stress differ from those in response to single stressors, and are genetically independent across traits in both males and females.

Phenotypic plasticity helps animals to buffer the effects of increasing thermal and nutritional stress created by climate change. Plastic responses to single and combined stressors can vary among genetically diverged populations. However, less is known about how plasticity in response to combined stress varies among individuals within a population or whether such variation changes across life-history traits. This is important because individual variation within populations shapes population-level responses to environmental change. Here, we used isogenic lines of Drosophila melanogaster to assess plasticity of egg-to-adult viability and sex-specific body size for combinations of two temperatures (25°C or 28°C) and three diets (standard diet, low caloric diet, or low protein:carbohydrate ratio diet). Our results reveal substantial within-population genetic variation in plasticity for egg-to-adult viability and wing size in response to combined thermal-nutritional stress. This genetic variation in plasticity was a result of cross-environment genetic correlations that were often < 1 for both traits, as well as changes in the expression of genetic variation across environments for egg-to-adult viability. Cross-sex genetic correlations for body size were weaker when the sexes were reared in different conditions, suggesting that the genetic basis of traits may change with the environment. Further, our results suggest that plasticity in egg-to-adult viability is genetically independent from plasticity in body size. Importantly, plasticity in response to diet and temperature individually differed from plastic shifts in response to diet and temperature in combination. By quantifying plasticity and the expression of genetic variance in response to combined stress across traits, our study reveals the complexity of animal responses to environmental change, and the need for a more nuanced understanding of the potential for populations to adapt to ongoing climate change.

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来源期刊
Journal of Evolutionary Biology
Journal of Evolutionary Biology 生物-进化生物学
CiteScore
4.20
自引率
4.80%
发文量
152
审稿时长
3-6 weeks
期刊介绍: It covers both micro- and macro-evolution of all types of organisms. The aim of the Journal is to integrate perspectives across molecular and microbial evolution, behaviour, genetics, ecology, life histories, development, palaeontology, systematics and morphology.
期刊最新文献
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