Willink Beatriz, Svensson Erik I
Department of Biology, Evolutionary Ecology Unit, Lund University, Ecology Building, Lund 223-62, Sweden
Department of Biology, Evolutionary Ecology Unit, Lund University, Ecology Building, Lund 223-62, Sweden.
Proc Biol Sci. 2017 Jan 25;284(1847). doi: 10.1098/rspb.2016.2407.
To understand host-parasite interactions, it is necessary to quantify variation and covariation in defence traits. We quantified parasite resistance and fitness tolerance of a polymorphic damselfly (Ischnura elegans), an insect with three discrete female colour morphs but with monomorphic males. We quantified sex and morph differences in parasite resistance (prevalence and intensity of water mite infections) and morph-specific fitness tolerance in the females in natural populations for over a decade. There was no evidence for higher parasite susceptibility in males as a cost of sexual selection, whereas differences in defence mechanisms between female morphs are consistent with correlational selection operating on combinations of parasite resistance and tolerance. We suggest that tolerance differences between female morphs interact with frequency-dependent sexual conflict, which maintains the polymorphism locally. Host-parasite interactions can therefore shape intra- and intersexual phenotypic divergence and interfere with sexual selection and sexual conflict.
为了理解宿主与寄生虫之间的相互作用,有必要对防御性状的变异和协变进行量化。我们对一种多态豆娘(优雅色蟌)的寄生虫抗性和适应耐受性进行了量化,这种昆虫有三种不同的雌性体色形态,但雄性为单态。在十多年的时间里,我们对自然种群中寄生虫抗性(水螨感染的流行率和强度)的性别和形态差异以及雌性的形态特异性适应耐受性进行了量化。没有证据表明雄性因性选择的代价而对寄生虫更易感,而雌性形态之间防御机制的差异与作用于寄生虫抗性和耐受性组合的相关选择是一致的。我们认为,雌性形态之间的耐受性差异与频率依赖性性冲突相互作用,从而在局部维持了多态性。因此,宿主 - 寄生虫相互作用可以塑造性别内和性别间的表型差异,并干扰性选择和性冲突。