Brace R C
Philos Trans R Soc Lond B Biol Sci. 1977 Feb 15;277(951):1-54. doi: 10.1098/rstb.1977.0006.
An account is given of the anatomy of a series of opisthobranch molluscs principally to assess the change in importance and functioning of the mantle cavity and columellar muscle throughout the transition from prosobranch to opisthobranch organization. Intermediate steps are represented by living tectibranchs, of which Philine and Scaphander are investigated in detail, Acteon, Bulla, Haminoea, Akera, Aglaja and Gastropteron more briefly. Though an opisthobranch, Acteon has an organization typical of a monotocardian prosobranch; the remainder show trends affecting the shell and visceral mass, mantle cavity and head-foot, which resulted finally in the production of nudibranch types. It is confirmed that the adaptations exhibited by primitive tectibranchs relate to the assumption of a burrowing mode of life. Initial changes were the reduction of the nuchal area and sealing of the mantle cavity anteriorly so that it opened on the right, where it became restricted, the first perhaps prompting the sealing. A broadening and an anterior elongation of the head-foot produced a wedge to facilitate burrowing. Change in disposition of the mantle edge, incurred by differential growth, produced an involute shell with a large body whorl, alignment changing from erect to horizontal. The resultant streamlining eased infaunal progression; no vertical insinking of the viscera was involved. Subsequently the shell became reduced and finally lost. A section of the mantle edge enlarged to produce a posterior mantle lobe upon which sit both the shell and viscera, and which later became redundant as posterior elongation of the head-foot produced a slug-like form, the viscera being incorporated within the head-foot. As the nuchal area became reduced, mechanical needs prompted alteration to both the form and attachment of the columellar muscle. In Acteon the muscle is like that of a prosobranch, but the proximal region has broadened, a change of proportion required by primitive tectibranchs in order to support the floor of the mantle cavity formed from the section of mantle skirt which in prosobranchs lies on the right. This was followed by reduction and re-alignment of the entire muscle along an anteroposterior axis as emphasis changed from the muscle effecting retraction into a shell to producing contorsions of the head-foot. The shell, similarly reduced, instead of providing anchorage, became itself anchored by additional anterior and posterior attachment zones with, in more advanced forms, dorsoventral muscles of the body wall rather than longitudinal muscles fastening to the former. Importance was placed on the mutual stabilization of constituent parts of the posterior body region. Re-alignments of the muscle induced breaking up of the longitudinal muscle sheet of the head-foot to produce muscle tracts, best exhibited in those tectibranchs which swim; they are derived from both the columellar muscle and intrinsic body wall muscles...
本文描述了一系列后鳃亚纲软体动物的解剖结构,主要目的是评估在从前鳃亚纲组织向后鳃亚纲组织转变的整个过程中,外套腔和柱状肌的重要性及功能变化。中间阶段以现存的裸鳃目动物为代表,其中对海兔属和囊螺属进行了详细研究,对阿神螺属、泡螺属、明螺属、艾氏海牛属、多彩海牛属和船蛸属的研究则相对简略。尽管阿神螺属属于后鳃亚纲,但具有典型的单心室前鳃亚纲的组织结构;其余的则呈现出影响贝壳和内脏团、外套腔以及头足部的变化趋势,最终导致了裸鳃类类型的产生。已证实原始裸鳃目动物所表现出的适应性与穴居生活方式的形成有关。最初的变化是颈部区域缩小,外套腔前端封闭,使其在右侧开口,且开口处变窄,前者可能促使了后者的封闭。头足部变宽并向前延伸形成一个楔子,便于挖掘。外套边缘位置的变化是由生长差异引起的,产生了一个具有大的体螺层的内卷贝壳,其排列从直立变为水平。由此产生的流线型结构便于在底内动物中前进;内脏没有垂直下陷。随后贝壳逐渐缩小并最终消失。外套边缘的一部分扩大形成一个后外套叶,贝壳和内脏都位于其上,后来随着头足部向后延伸形成蛞蝓状形态,内脏并入头足部,后外套叶变得多余。随着颈部区域缩小,机械需求促使柱状肌的形态和附着方式发生改变。在阿神螺属中,肌肉与前鳃亚纲的相似,但近端区域变宽,这是原始裸鳃目动物为了支撑由外套裙部分形成的外套腔底部而需要的比例变化,在前鳃亚纲中,外套裙部分位于右侧。随后,随着重点从影响贝壳收缩的肌肉转变为使头足部产生扭转的肌肉,整个肌肉沿着前后轴缩小并重新排列。同样缩小的贝壳不再提供锚固作用,而是通过额外的前后附着区域固定自身,在更高级的形式中,由体壁的背腹肌肉而非纵向肌肉固定在原来的位置。重点在于后体区域各组成部分的相互稳定。肌肉的重新排列导致头足部纵向肌层分裂形成肌束,在那些能够游泳的裸鳃目动物中表现得最为明显;它们源自柱状肌和体壁固有肌肉……