Stewart James R
Department of Biological Sciences, East Tennessee State University, Johnson City, TN 37614, USA.
J Morphol. 2013 Jul;274(7):824-43. doi: 10.1002/jmor.20141. Epub 2013 Mar 21.
The primary pattern of embryonic nutrition for squamate reptiles is lecithotrophy; with few exceptions, all squamate embryos mobilize nutrients from yolk. The evolution of viviparity presents an opportunity for an additional source of embryonic nutrition through delivery of uterine secretions, or placentotrophy. This pattern of embryonic nutrition is thought to evolve through placental supplementation of lecithotrophy, followed by increasing dependence on placentotrophy. This review analyzes the relationship between reproductive mode and pattern of embryonic nutrition in three lecithotrophic viviparous species, and oviparous counterparts, for concordance with a current model for the evolution of viviparity and placentation. The assumptions of the model, that nutrients for oviparous embryos are mobilized from yolk, and that this source is not disrupted in the transition to viviparity, are supported for most nutrients. In contrast, calcium, an essential nutrient for embryonic development, is mobilized from both yolk and eggshell by oviparous embryos and reduction of eggshell calcium is correlated with viviparity. If embryonic fitness is compromised by disruption of a primary source of calcium, selection may not favor evolution of viviparity, yet viviparity has arisen independently in numerous squamate lineages. Studies of fetal nutrition in reproductively bimodal species suggest a resolution to this paradox. If uterine calcium secretion occurs during prolonged intrauterine egg retention, calcium placentotrophy evolves prior to viviparity as a replacement for eggshell calcium and embryonic nutrition will not be compromised. This hypothesis is integrated into the current model for evolution of viviparity and placentation to address the unique attributes of calcium nutrition. The sequence of events requires a shift in timing of uterine calcium secretion and the embryonic mechanism of calcium retrieval to be responsive to calcium availability. Regulation of uterine calcium secretion and the mechanism of embryonic uptake of calcium are important elements to understanding evolution of viviparity and placentation.
有鳞目爬行动物胚胎营养的主要模式是卵黄营养;除少数例外,所有有鳞目胚胎都从卵黄中获取营养。胎生的进化为通过子宫分泌物提供额外的胚胎营养源创造了机会,即胎盘营养。这种胚胎营养模式被认为是通过胎盘对卵黄营养的补充而进化而来的,随后对胎盘营养的依赖性不断增加。本综述分析了三种卵黄营养型胎生物种及其卵生对应物种的生殖模式与胚胎营养模式之间的关系,以验证当前关于胎生和胎盘形成进化的模型。该模型的假设,即卵生胚胎的营养来自卵黄,并且在向胎生的转变过程中这个来源不会受到干扰,在大多数营养物质方面得到了支持。相比之下,钙是胚胎发育必需的营养物质,卵生胚胎从卵黄和蛋壳中获取钙,蛋壳钙的减少与胎生相关。如果胚胎的健康因主要钙源的中断而受到损害,选择可能不利于胎生的进化,但胎生在众多有鳞目谱系中独立出现。对具有两种生殖模式物种的胎儿营养研究为这一矛盾提供了解决方案。如果在子宫内长时间保留卵的过程中发生子宫钙分泌,钙胎盘营养在胎生之前就会进化,以替代蛋壳钙,胚胎营养不会受到影响。这一假设被纳入当前关于胎生和胎盘形成进化的模型中,以解决钙营养的独特属性问题。事件的顺序需要子宫钙分泌时间的转变以及胚胎钙摄取机制对钙可用性的响应。子宫钙分泌的调节和胚胎钙摄取的机制是理解胎生和胎盘形成进化的重要因素。