Jamieson B G M
Department of Zoology, University of Queensland, Brisbane, Queensland, Australia 4067.
Cladistics. 1988 Dec;4(4):367-401. doi: 10.1111/j.1096-0031.1988.tb00520.x.
Abstract- The 50 oligochaete taxa representing all families of "opisthoporous" oligochaetes (Aliuroididae, earthworms and aquatic "megadriles") together with two representatives of the Haplotaxidac and three examples of "microdiles" were subjected to cladistic analysis using the PAUP program. Sixty-eight characters used in the analyses were derived from a comprehensive range of somatic and genital systems. The optimal result, in terms of maximal number of characters and taxa and of parsimony, produced two trees (consistency index 0.362) differing only in the placement of the monotypic clade for the family Lumbriculidae. From a line originating from the presumed octogonadial ancestor, the following branches were derived, in sequence from the basal to most derived (new taxa asterisked): subclass Randiellata* (order Randiellida*, Randiellidae); subclass Tubificata* (order Tubificida, Tubincidae, Naididae computed and others not computed); subclass Lumbriculata* (order Lumbriculida, Lumbriculidae); superorder Haplotaxidea* (order Haplotaxida, Haplotaxidae); order Moniligastrida (Moniligastridae); suborder Alluroidina (Aliuroididae and Syngenodrilidae); cohort Aquamegadrili* (with, in succession, superfamilice Sparganophiloidea, Sparganophilidae; Biwadriloidea, Biwadrilidac, and Almoidca-Lutodrilidac and Almidae, including Criodrilus); superfamily Eudriloidea*, superfamily Lumbricoidea and, as the adelphotaxon of the latter, the superfamily Megascolecoidea. Intermediate nodes were given the following names, with the adelpholaxon through to the Megascolecoidea, M, in parentheses: subclass Diplotesticulata (Haplotaxidea-M); superorder Metagynopohora* (Moniligastrida-M); order Opisthopora (Alluroidina M); suborder Crassiclitellata* (Aquamegadrili - M); cohort Terrimegadrili* (Ocnerodriloidea M); unnamed (Eudriloidea M); unnamed (Lumbricoidea and Megascolecoidea). Recognition of the Randiellata, which alone were added intuitively and not computed, and the position of the Lumbriculata, are tentative. Location of the Lumbricoidea as the adelphotaxon of a restricted Megascoecloidea is heuristic, but the alternative depiction of lumbricoids in some analyses, as the adelphotaxon of an ocnerodrilid-eudrilid-megascolecoid clade (the conventional Megascolecoidea s. lat.), is not conclusively dismissed.
摘要——代表“后孔寡毛类”所有科(异尾蚓科、蚯蚓和水生“巨蚓类”)的50个寡毛类分类单元,连同单毛类的两个代表以及“微蚓类”的三个实例,使用PAUP程序进行了分支分析。分析中使用的68个特征源自广泛的躯体和生殖系统。就特征和分类单元的最大数量以及简约性而言,最优结果产生了两棵树(一致性指数为0.362),仅在颤蚓科单型分支的位置上有所不同。从假定的八性腺祖先起源的一条谱系中,依次衍生出以下分支,从基部到最衍生(新分类单元加星号):兰氏寡毛亚纲*(兰氏寡毛目*、兰氏寡毛科);颤蚓亚纲*(颤蚓目、颤蚓科、计算在内的仙女虫科及其他未计算的科);颤蚓亚纲*(颤蚓目、颤蚓科);单毛超目*(单毛目、单毛科);链胃蚓目(链胃蚓科);异尾蚓亚目(异尾蚓科和同腺蚓科);水生巨蚓类*(依次有大蛭超科、大蛭科;双线蚓超科、双线蚓科,以及阿尔莫蚓-泥蚓科和阿尔莫科,包括颤蚓属);真蚓超科*、环毛蚓超科,以及作为后者姐妹分类单元的巨蚓超科。中间节点被赋予以下名称,从姐妹分类单元到巨蚓超科,用括号中的M表示:双睾丸亚纲(单毛目-M);后雌孔超目*(链胃蚓目-M);后孔目(异尾蚓亚目-M);厚环带亚目*(水生巨蚓类-M);陆生巨蚓类*(奥氏蚓超科-M);未命名(真蚓超科-M);未命名(环毛蚓超科和巨蚓超科)。兰氏寡毛亚纲是直观添加而非计算得出的,其识别以及颤蚓亚纲的位置是暂定的。将环毛蚓超科作为狭义巨蚓超科的姐妹分类单元的定位是试探性的,但在某些分析中,将环毛蚓类作为奥氏蚓-真蚓-巨蚓类分支(传统的广义巨蚓超科)的姐妹分类单元的另一种描述并未被最终否定。