Evolutionary Stress Ecology and Ecotoxicology, University of Leuven, Leuven, Belgium.
J Anim Ecol. 2020 Jul;89(7):1711-1721. doi: 10.1111/1365-2656.13235. Epub 2020 Apr 28.
Species typically align along a fast-slow life-history continuum, yet it is not clear to what extent oxidative stress physiology can be integrated with this continuum to form a 'pace-of-life syndrome', especially so in invertebrates. This is important, given the assumed role of oxidative stress in mediating life-history trade-offs, and the prediction that species with a faster pace should be more vulnerable to oxidative stress. We tested whether a species' life-history pace, here represented by its growth rate, can predict species-level differentiation in physiology and sensitivity to oxidative stress. Therefore, we exposed four species of Ischnura damselflies that strongly align along a fast-slow life-history continuum to different levels of ultraviolet (UV) radiation. We measured an extended set of physiological traits linked to the pace-of-life: standard metabolic rate, oxidative stress physiology (antioxidant enzymes and oxidative damage) and defence/condition traits (investment in immune function, energy storage and structural defence). Despite strong species differences in growth rate and physiology, growth rate did not predict species-level differentiation in physiology. Hence there was no support for the integration of metabolic rate, oxidative stress physiology or defence/condition traits into a species-level syndrome. Ultraviolet exposure affected nearly all traits: it reduced growth rate and increased metabolic rate, affected all oxidative stress physiology traits and increased the two defence traits (immune function, and melanin content). Nevertheless, the pace-of-life based on growth rate did not predict sensitivity to UV. Instead, the observed pattern of investment in structural UV defence (melanin) might have reduced the need for enzymatic antioxidant defence, this way potentially decoupling the covariation between the life-history pace and oxidative stress physiology. The absence of an integrated axis of life-history and physiological variation indicates no major constraints for the evolution of these traits among the studied damselfly species. Our study highlights that ecological differences between species may decouple covariation between species' life-history pace and their physiology, as well as their sensitivity to environmental stressors.
物种通常沿着快速-缓慢的生活史连续体排列,但目前尚不清楚氧化应激生理学在多大程度上可以与这一连续体整合形成“生活史综合征”,尤其是在无脊椎动物中。这很重要,因为氧化应激被认为在介导生活史权衡中起着重要作用,并且预测具有更快节奏的物种应该更容易受到氧化应激的影响。我们测试了一个物种的生活史节奏,这里用它的生长速度来表示,是否可以预测物种水平的生理分化和对氧化应激的敏感性。因此,我们将四个强烈沿着快速-缓慢生活史连续体排列的豆娘蜻属蜻蜓暴露在不同水平的紫外线 (UV) 辐射下。我们测量了一组与生活史节奏相关的扩展生理特征:标准代谢率、氧化应激生理学(抗氧化酶和氧化损伤)和防御/状态特征(免疫功能、能量储存和结构防御的投资)。尽管生长速度和生理特性存在明显的物种差异,但生长速度并不能预测生理水平的物种分化。因此,代谢率、氧化应激生理学或防御/状态特征没有整合到物种水平的综合征中。紫外线照射几乎影响了所有的特征:它降低了生长速度,增加了代谢率,影响了所有的氧化应激生理学特征,并增加了两个防御特征(免疫功能和黑色素含量)。然而,基于生长速度的生活史节奏并不能预测对 UV 的敏感性。相反,观察到的结构 UV 防御(黑色素)的投资模式可能减少了对酶抗氧化防御的需求,从而潜在地使生活史节奏和氧化应激生理学之间的协变脱钩。生活史和生理变异综合轴的缺失表明,在所研究的蜻蜓物种中,这些特征的进化没有主要的限制。我们的研究强调了物种间的生态差异可能会使物种的生活史节奏与其生理学以及对环境胁迫的敏感性之间的协变脱钩。