Braz Henrique B, Almeida-Santos Selma M, Murphy Christopher R, Thompson Michael B
School of Life and Environmental Sciences, University of Sydney, Sydney, Australia.
Laboratório de Ecologia e Evolução, Instituto Butantan, São Paulo, Brazil.
J Exp Zool B Mol Dev Evol. 2018 May;330(3):165-180. doi: 10.1002/jez.b.22800. Epub 2018 Apr 14.
The evolution of viviparity requires eggshell thinning to bring together the maternal uterus and extraembryonic membranes to form placentae for physiological exchanges. Eggshell thinning likely involves reduced activity of the uterine glands that secrete it. We tested these hypotheses by comparing the uterine and eggshell structure and histochemistry among oviparous and viviparous water snakes (Helicops) using phylogenetic methods. Eggshell thinning occurred convergently in all three origins of viviparity in Helicops and was accomplished by the loss of the mineral layer and thinning of the shell membrane. Uterine glands secrete the shell membrane in both oviparous and viviparous Helicops. These glands increase during vitellogenesis regardless of the reproductive mode, but they always reach smaller sizes in viviparous forms. As there is no phylogenetic signal in eggshell thickness and gland dimensions, we conclude that interspecific differences are related to reproductive mode and not phylogeny. Therefore, our results support the hypothesis that eggshell thinning is associated with the evolution of viviparity and that such thinning result from a reduction in gland size in viviparous taxa. Interestingly, the shell membrane thickness of viviparous females of the reproductively bimodal Helicops angulatus is intermediate between their oviparous and viviparous congeners. Thus, although eggshell thinning is required by the evolution of viviparity, a nearly complete loss of this structure is not. However, uterine gland dimensions are similar across viviparous Helicops. Fewer glands or their functional repurposing may explain the thinner shell membrane in viviparous species of Helicops in comparison to viviparous females of the bimodal H. angulatus.
胎生的进化需要蛋壳变薄,以使母体子宫和胚外膜结合在一起,形成用于生理交换的胎盘。蛋壳变薄可能涉及分泌蛋壳的子宫腺活性降低。我们通过系统发育方法比较了卵生和胎生水蛇(Helicops)的子宫和蛋壳结构及组织化学,来检验这些假设。在Helicops的所有三个胎生起源中,蛋壳变薄是趋同发生的,是通过矿物质层的丧失和壳膜变薄实现的。在卵生和胎生的Helicops中,子宫腺都分泌壳膜。无论生殖模式如何,这些腺体在卵黄发生期间都会增加,但在胎生形式中它们的大小总是较小。由于蛋壳厚度和腺体大小没有系统发育信号,我们得出结论,种间差异与生殖模式有关,而非系统发育。因此,我们的结果支持了这样的假设,即蛋壳变薄与胎生的进化有关,并且这种变薄是由于胎生类群中腺体大小的减小。有趣的是,具有两种生殖模式的角Helicops胎生雌性的壳膜厚度介于其卵生和胎生同属之间。因此,虽然胎生的进化需要蛋壳变薄,但这种结构并非几乎完全丧失。然而,胎生的Helicops的子宫腺大小相似。腺体数量减少或其功能的重新利用可能解释了与具有两种生殖模式的角Helicops胎生雌性相比,Helicops胎生物种的壳膜更薄的原因。