Department of Evolutionary Biology, Integrative Zoology, Faculty of Life Sciences, University of Vienna, Vienna, 1090, Austria.
Department of Palaeontology, Faculty of Earth Sciences, Geography and Astronomy, University of Vienna, Vienna, 1090, Austria.
Biol Rev Camb Philos Soc. 2020 Jun;95(3):696-729. doi: 10.1111/brv.12583. Epub 2020 Feb 7.
Molecular techniques are currently the leading tools for reconstructing phylogenetic relationships, but our understanding of ancestral, plesiomorphic and apomorphic characters requires the study of the morphology of extant forms for testing these phylogenies and for reconstructing character evolution. This review highlights the potential of soft body morphology for inferring the evolution and phylogeny of the lophotrochozoan phylum Bryozoa. This colonial taxon comprises aquatic coelomate filter-feeders that dominate many benthic communities, both marine and freshwater. Despite having a similar bauplan, bryozoans are morphologically highly diverse and are represented by three major taxa: Phylactolaemata, Stenolaemata and Gymnolaemata. Recent molecular studies resulted in a comprehensive phylogenetic tree with the Phylactolaemata sister to the remaining two taxa, and Stenolaemata (Cyclostomata) sister to Gymnolaemata. We plotted data of soft tissue morphology onto this phylogeny in order to gain further insights into the origin of morphological novelties and character evolution in the phylum. All three larger clades have morphological apomorphies assignable to the latest molecular phylogeny. Stenolaemata (Cyclostomata) and Gymnolaemata were united as monophyletic Myolaemata because of the apomorphic myoepithelial and triradiate pharynx. One of the main evolutionary changes in bryozoans is a change from a body wall with two well-developed muscular layers and numerous retractor muscles in Phylactolaemata to a body wall with few specialized muscles and few retractors in the remaining bryozoans. Such a shift probably pre-dated a body wall calcification that evolved independently at least twice in Bryozoa and resulted in the evolution of various hydrostatic mechanisms for polypide protrusion. In Cyclostomata, body wall calcification was accompanied by a unique detachment of the peritoneum from the epidermis to form the hydrostatic membraneous sac. The digestive tract of the Myolaemata differs from the phylactolaemate condition by a distinct ciliated pylorus not present in phylactolaemates. All bryozoans have a mesodermal funiculus, which is duplicated in Gymnolaemata. A colonial system of integration (CSI) of additional, sometimes branching, funicular cords connecting neighbouring zooids via pores with pore-cell complexes evolved at least twice in Gymnolaemata. The nervous system in all bryozoans is subepithelial and concentrated at the lophophoral base and the tentacles. Tentacular nerves emerge intertentacularly in Phylactolaemata whereas they partially emanate directly from the cerebral ganglion or the circum-oral nerve ring in myolaemates. Overall, morphological evidence shows that ancestral forms were small, colonial coelomates with a muscular body wall and a U-shaped gut with ciliary tentacle crown, and were capable of asexual budding. Coloniality resulted in many novelties including the origin of zooidal polymorphism, an apomorphic landmark trait of the Myolaemata.
分子技术目前是重建系统发育关系的主要工具,但我们对祖先、原始和衍生特征的理解需要研究现存形式的形态,以检验这些系统发育关系并重建特征进化。本综述强调了软体制图在推断苔藓动物门苔藓动物的进化和系统发育中的潜力。这个殖民地分类群由水生后生动物滤食动物组成,在海洋和淡水的许多底栖群落中占主导地位。尽管具有相似的体模式,但苔藓动物在形态上高度多样化,分为三大类:Phylactolaemata、Stenolaemata 和 Gymnolaemata。最近的分子研究产生了一个全面的系统发育树,其中 Phylactolaemata 与其余两个类群的姐妹关系,Stenolaemata(环口动物)与 Gymnolaemata 的姐妹关系。我们将软组织形态的数据绘制在这个系统发育树上,以进一步了解该门形态新颖性和特征进化的起源。所有三个较大的分支都有可分配给最新分子系统发育的形态衍生特征。Stenolaemata(环口动物)和 Gymnolaemata 因具有形态衍生的肌上皮和三叉咽而被联合为单系 Myolaemata。苔藓动物的主要进化变化之一是,在 Phylactolaemata 中,从具有两个发育良好的肌肉层和许多收缩肌的体壁转变为在其余苔藓动物中具有较少专门肌肉和较少收缩肌的体壁。这种转变可能早于至少在苔藓动物中独立进化两次的体壁钙化,导致了各种用于息肉突出的流体静力机制的进化。在环口动物中,体壁钙化伴随着腹膜从表皮的独特分离,形成流体静力膜囊。Myolaemata 的消化道与 phylactolaemate 状态不同,具有明显的纤毛幽门,phylactolaemate 中不存在。所有苔藓动物都有中胚层索,在 Gymnolaemata 中则被复制。通过带有孔细胞复合体的孔连接相邻体腔的额外的、有时分支的索状索的群体系统整合(CSI)在 Gymnolaemata 中至少进化了两次。所有苔藓动物的神经系统都是上皮下的,集中在叶状基础和触须上。在 Phylactolaemata 中,触须神经从触须间出现,而在 Myolaemata 中,它们部分直接从脑神经节或环绕口神经环发出。总的来说,形态学证据表明,祖先形式是小型后生动物,具有肌肉体壁和 U 形肠道,具有纤毛触须冠,能够进行无性芽殖。群体生活导致了许多新颖性,包括起源于 Myolaemata 的形态衍生特征的体腔多态性。