Posgrado en Ciencias Biológicas, Instituto de Ecología, Universidad Nacional Autónoma de México , México , Distrito Federal , Mexico.
Departamento de Ecología Evolutiva, Instituto de Ecología, Universidad Nacional Autónoma de México , Distrito Federal , Mexico.
PeerJ. 2014 Jan 30;2:e247. doi: 10.7717/peerj.247. eCollection 2014.
Signa are sclerotized structures located on the inner wall of the corpus bursa of female Lepidoptera whose main function is tearing open spermatophores. The sexually antagonistic coevolution (SAC) hypothesis proposes that the thickness of spermatophore envelopes has driven the evolution of the females signa; this idea is based in the fact that in many lepidopterans female sexual receptivity is at least partially controlled by the volume of ejaculate remaining in the corpus bursa. According to the SAC hypothesis, males evolved thick spermatophore envelopes to delay the post-mating recovery of female sexual receptivity thus reducing sperm competition; in response, females evolved signa for breaking spermatophore envelopes faster, gaining access to the resources contained in them and reducing their intermating intervals; the evolution of signa, in turn, favored the evolution of even thicker spermatophore envelopes, and so on. We tested two predictions of the SAC hypothesis with comparative data on the thickness of spermatophore envelopes of eleven species of Heliconiinae butterflies. The first prediction is that the spermatophore envelopes of polyandrous species with signa will be thicker than those of monandrous species without signa. In agreement with this prediction, we found that the spermatophore envelopes of a polyandrous Heliconius species with signa are thicker than those of two monandrous Heliconius species without signa. The second prediction is that in some species with signa males could enforce monandry in females by evolving "very thick" spermatophore envelopes, in these species we predict that their spermatophore envelopes will be thicker than those of their closer polyandrous relatives with signa. In agreement with this prediction, we found that in two out of three comparisons, spermatophore envelopes of monandrous species with signa have thicker spermatophore envelopes than their closer polyandrous relatives with signa. Thus, our results support the idea that selective pressures arising from sexually antagonistic interactions have been important in the evolution of spermatophore envelopes, female signa and female mating patterns.
信号是位于雌性鳞翅目昆虫的囊体内壁的硬化结构,其主要功能是撕开精包。性拮抗协同进化(SAC)假说提出,精包包膜的厚度推动了雌性信号的进化;这一观点基于这样一个事实,即在许多鳞翅目昆虫中,雌性的性接受能力至少部分受到储存在囊体中的精液量的控制。根据 SAC 假说,雄性进化出厚的精包包膜,以延迟交配后雌性性接受能力的恢复,从而减少精子竞争;作为回应,雌性进化出更快地撕开精包包膜的信号,以获取其中包含的资源并减少它们的交配间隔;信号的进化反过来又促进了更厚的精包包膜的进化,以此类推。我们用 11 种 Heliconiinae 蝴蝶的精包包膜厚度的比较数据来检验 SAC 假说的两个预测。第一个预测是,具有信号的多配偶物种的精包包膜比没有信号的单配偶物种的精包包膜更厚。与这一预测一致,我们发现具有信号的多配偶 Heliconius 物种的精包包膜比没有信号的两个单配偶 Heliconius 物种的精包包膜更厚。第二个预测是,在一些具有信号的物种中,雄性可以通过进化“非常厚”的精包包膜来强制雌性单配偶,在这些物种中,我们预测它们的精包包膜会比具有信号的近亲更厚。与这一预测一致,我们发现,在三个比较中的两个中,具有信号的单配偶物种的精包包膜比具有信号的近亲更厚。因此,我们的结果支持这样一种观点,即来自性拮抗相互作用的选择压力在精包包膜、雌性信号和雌性交配模式的进化中一直很重要。