Scherholz Maik, Redl Emanuel, Wollesen Tim, Todt Christiane, Wanninger Andreas
Department of Integrative Zoology, Faculty of Life Sciences, University of Vienna, Althanstraße 14, 1090, Vienna, Austria.
University Museum of Bergen, University of Bergen, Allégaten 41, 5007, Bergen, Norway.
BMC Evol Biol. 2015 Sep 18;15:201. doi: 10.1186/s12862-015-0467-1.
Recent studies suggest a bifurcation at the base of Mollusca, resulting in the primarily single-shelled Conchifera (Bivalvia, Gastropoda, Scaphopoda, Monoplacophora, Cephalopoda) and the spicule-bearing Aculifera (Polyplacophora, Neomeniomorpha, Chaetodermomorpha). A recent study revealed a complex larval musculature exclusively shared by Neomeniomorpha and Polyplacophora, supporting a close relationship of both taxa. However, the ontogenetic transition from the complex larval to the simple adult neomeniomorph musculature, which mainly consists of a three-layered body-wall musculature and serially iterated dorsoventral muscles, remains unknown. To close this gap in knowledge, we studied remodeling of the larval musculature during metamorphosis in the neomeniomorph Wirenia argentea. A comparative analysis with a novel data set of a polyplacophoran, Leptochiton asellus, allows us to infer the morphology of the last common ancestor of Aculifera and the evolution of its subclades therefrom.
The complex larval musculature of Wirenia argentea persists through metamorphosis and becomes modified to form two of the three muscle layers of the adult body wall. The innermost longitudinal layer of the three-layered body wall musculature is generated by transformation and expansion of distinct larval longitudinal muscle bundles. The larval ventrolateral muscle strands are remodeled and eventually become the most ventral part of the adult longitudinal layer of the body wall musculature. The paired larval enrolling muscle forms the lateral parts and the former rectus muscle is destined to become the most dorsal part of the longitudinal layer of the body wall musculature. The transient ventromedian muscle is lost during postmetamorphic development.
Postmetamorphic remodeling in W. argentea supports the hypothesis of a complex myoanatomy rather than a three-layered body wall musculature at the base of Aculifera, and thus argues against homology of the body wall musculature of adult Neomeniomorpha and other potential molluscan sister groups. Our data show that the neomeniomorph body wall musculature is a derived condition and not an aculiferan or molluscan plesiomorphy.
近期研究表明软体动物基部存在一个分支,产生了主要为单壳的有壳类(双壳纲、腹足纲、掘足纲、单板纲、头足纲)和具骨针的无板类(多板纲、新蝶贝目、毛肤石鳖目)。一项近期研究揭示了新蝶贝目和多板纲独有的复杂幼虫肌肉组织,支持了这两个分类单元的密切关系。然而,从复杂的幼虫肌肉组织到简单的成年新蝶贝目肌肉组织的个体发育转变,其主要由三层体壁肌肉组织和一系列背腹肌肉组成,仍然未知。为了填补这一知识空白,我们研究了新蝶贝目银新蝶(Wirenia argentea)变态过程中幼虫肌肉组织的重塑。与多板纲的小笠原薄石鳖(Leptochiton asellus)的一个新数据集进行比较分析,使我们能够推断无板类最后一个共同祖先的形态及其亚分支的进化。
银新蝶的复杂幼虫肌肉组织在变态过程中持续存在,并经过修饰形成成年体壁三层肌肉中的两层。三层体壁肌肉组织的最内层纵向层由不同的幼虫纵向肌束转变和扩展形成。幼虫腹外侧肌束经过重塑,最终成为体壁肌肉组织成年纵向层的最腹侧部分。成对的幼虫卷曲肌形成外侧部分,原来的直肠肌注定成为体壁肌肉组织纵向层的最背侧部分。短暂的腹中线肌在变态后发育过程中消失。
银新蝶变态后的重塑支持了在无板类基部存在复杂肌解剖结构而非三层体壁肌肉组织的假设,因此反对成年新蝶贝目与其他潜在软体动物姐妹类群体壁肌肉组织的同源性。我们的数据表明,新蝶贝目体壁肌肉组织是一种衍生状态,而非无板类或软体动物的原始特征。