Lin M F, Leise E M
Department of Biology, University of North Carolina Greensboro 27412-5001, USA.
J Comp Neurol. 1996 Oct 14;374(2):180-93. doi: 10.1002/(SICI)1096-9861(19961014)374:2<180::AID-CNE2>3.0.CO;2-Z.
We determined that the larval nervous system of Ilyanassa obsoleta contains paired cerebral, pleural, pedal, buccal and intestinal ganglia and unpaired apical, osphradial, and visceral ganglia. We used a modified form of NADPH diaphorase histochemistry to compare the neuroanatomy of precompetent (including specimens 6, 8, and 12 days after hatching), competent, and metamorphosing larvae with postmetamorphic juveniles. This method highlighted ganglionic neuropils and allowed us to identify individual ganglia at various stages of development, thereby laying a foundation for concurrent histochemical studies. The first ganglia to form were the unpaired apical and osphradial ganglia and the paired cerebral and pedal ganglia. In larvae 6 days after hatching, the neuropil had already appeared in the apical and osphradial ganglia. Neuropil began to be apparent in the cerebral and pedal ganglia 2 days later. At that time, the pleural and buccal ganglia were identifiable and adjacent to the posterior edge of the cerebral ganglia. The ganglia of the visceral loop were concurrently recognizable, although the supraintestinal ganglion developed slightly earlier than the subintestinal and visceral ganglia. By 12 days after hatching all of the major adult ganglia were discernible. The apical ganglion was retained by newly metamorphosed juveniles, but not by juveniles 2 days later. After metamorphosis was complete, the central nervous system (CNS) was consolidated into its juvenile form with ipsilateral cerebral and pleural ganglia being partially fused. The metamorphic translocation of ganglia, which included a caudal relocation of the cerebrals and the migration of the buccals from above the esophagus to a position below it, correlated with the movement of the proboscis to the dorsal part of the head.
我们确定,过时泥螺的幼虫神经系统包含成对的脑、胸膜、足、口和肠神经节以及不成对的顶、嗅检器和内脏神经节。我们使用改良形式的NADPH黄递酶组织化学方法,比较了具备能力前(包括孵化后6、8和12天的标本)、具备能力和变态期幼虫与变态后幼体的神经解剖结构。该方法突出了神经节的神经纤维网,使我们能够识别发育各阶段的单个神经节,从而为同步组织化学研究奠定了基础。最早形成的神经节是不成对的顶神经节和嗅检器神经节以及成对的脑和足神经节。在孵化后6天的幼虫中,神经纤维网已出现在顶神经节和嗅检器神经节中。两天后,神经纤维网开始在脑和足神经节中显现。此时,胸膜和口神经节可被识别,并与脑神经节的后缘相邻。内脏环的神经节同时也可辨认,尽管肠上神经节比肠下神经节和内脏神经节发育稍早。到孵化后12天时,所有主要的成体神经节都清晰可辨。新变态的幼体保留了顶神经节,但两天后的幼体则没有。变态完成后,中枢神经系统(CNS)整合为幼体形式,同侧的脑和胸膜神经节部分融合。神经节的变态移位,包括脑的尾向移位以及口神经节从食管上方迁移到其下方的位置,与吻向头部背侧的移动相关。