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The origin of the pelagobenthic metazoan life cycle: what's sex got to do with it?

机译:骨盆底后生动物生命周期的起源:性与它有什么关系?

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The biphasic (pelagobenthic) life cycle is found throughout the animal kingdom, and includes gametogenesis, embryogenesis, and metamorphosis. From a tangled web of hypotheses on the origin and evolution of the metazoan pelagobenthic life cycle, current opinion appears to favor a simple, larval-like holopelagic ancestor that independently settled multiple times to incorporate a benthic phase into the life cycle. This hypothesis derives originally from Haeckel's (1874) Gastraea theory of ontogeny recapitulating phylogeny, in which the gastrula is viewed as the recapitulation of a gastraean ancestor that evolved via selection on a simple, planktonic hollow ball of cells to develop the capacity to feed. Here, we propose an equally plausible hypothesis that the origin of the metazoan pelagobenthic life cycle was a direct consequence of sexual reproduction in a likely holobenthic ancestor. In doing so, we take into account new insights from poriferan development and from molecular phylogenies. In this scenario, the gastrula does not represent a recapitulation, but simply an embryological stage that is an outcome of sexual reproduction. The embryo can itself be considered as the precursor to a biphasic lifestyle, with the embryo representing one phase and the adult another phase. This hypothesis is more parsimonious because it precludes the need for multiple, independent origins of the benthic form. It is then reasonable to consider that multilayered, ciliated embryos ultimately released into the water column are subject to natural selection for dispersal/longevity/feeding that sets them on the evolutionary trajectory towards the crown metazoan planktonic larvae. These new insights from poriferan development thus clearly support the intercalation hypothesis of bilaterian larval evolution, which we now believe should be extended to discussions of the origin of biphasy in the metazoan last common ancestor.
机译:在整个动物界中都发现了双相的(pelagobenthic)生命周期,包括配子发生,胚胎发生和变态。从关于后生动物兜底栖动物生命周期起源和进化的假说错综复杂的网络中,当前的观点似乎倾向于一个简单的,类似幼虫的石斑鱼祖先,该祖先独立地定居了多次,以将底栖生物阶段纳入生命周期。该假设最初源自Haeckel(1874)的胃口生殖器重现系统发育学说,其中胃is被认为是胃胃祖先的概要生活,其通过在一个简单的浮游性空心细胞球上进行选择而进化,从而提高了觅食的能力。在这里,我们提出了一个同样合理的假设,即后生的兽足生命周期的起源是在可能的整体性祖先中有性生殖的直接结果。在此过程中,我们考虑了卟啉开发和分子系统发育的新见解。在这种情况下,下腹并不代表重演,而仅仅是有性生殖的结果。胚胎本身可以被认为是双相生活方式的先驱,胚胎代表一个阶段,成年则代表另一个阶段。该假设更为简洁,因为它排除了对底栖形式的多个独立起源的需求。因此,有理由认为,最终释放到水柱中的多层纤毛胚胎要经过自然选择才能扩散/长寿/进食,这使它们处于朝向后生冠状浮游幼虫的进化轨迹上。因此,这些来自poriferan发育的新见解清楚地支持了bilaterian幼虫进化的插层假说,我们现在认为,该假说应扩展到对后生后生共同祖先中biphasy起源的讨论。

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