Department of Zoology, Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom.
Int J Parasitol. 2012 Jan;42(1):71-92. doi: 10.1016/j.ijpara.2011.10.009. Epub 2011 Nov 25.
Poecilostome cyclopoids are among the most morphologically diverse copepods, having established symbiotic relationships with teleosts, elasmobranchs and invertebrate hosts belonging to no fewer than 14 marine phyla. Many parasitic lineages display radically divergent body plans and on that basis have traditionally been placed at higher taxonomic rank than they deserve. The most recent example is the monotypic family Umazuracolidae, established for a derived fish parasite with bomolochiform affinities. Phylogenetic analysis of complete ssrDNA (18S) sequences of 44 species belonging to 21 families of cyclopoid copepods shows that there is no support for the familial distinctiveness of the Umazuracolidae. Both maximum parsimony tree reconstruction and Bayesian inference, operating under the GTR+I+Γ model of nucleotide substitution, unambiguously placed Umazuracola elongatus in the Taeniacanthidae within the predominantly fish parasitic bomolochiform complex, refuting the original suggestion of a shared most recent common ancestry with polychaete symbionts. The phylogenies also revealed that the bomolochiform families and the Clausidiidae (and allies) form a monophyletic group, the clausidiiform complex, with high nodal support under both methods. Bayesian inference suggested a diphyletic origin of the "Poecilostomatoida" with the clausidiiform family-group holding a basal position while the traditional cyclopoid families form a monophyletic group in apposition to a second poecilostomatoid clade; however, maximum parsimony results were equivocal, depending on outgroup selection. Scrutiny of the morphological characters diagnosing the monotypic families Tegobomolochidae and Tuccidae demonstrated that they merely represent derived lineages within more inclusive taxa, the former being related to a group of nostril-inhabiting genera within the Bomolochidae, the latter forming the sistergroup of Taeniacanthodes within the Taeniacanthidae. The taeniacanthid genus Makrostrotos occupies a position at the base of the bomolochiform complex and is fixed as the type of a new family, Makrostrotidae. Although both morphological and molecular evidence hint that the Bomolochidae is nested within a paraphyletic Taeniacanthidae, the status quo of maintaining both families is favoured here pending additional molecular data. The bomolochiform complex, comprising the Bomolochidae, Taeniacanthidae, Telsidae and Makrostrotidae, is attributed superfamilial rank as the Bomolochoidea. A recent controversial phylogenetic analysis of the poecilostomatoid families is shown to be flawed, being based on a dataset containing imperfect or misleading information, and characters whose states were wrongly assessed.
镖水蚤目是形态最多样化的桡足类之一,与硬骨鱼、软骨鱼和至少 14 个海洋门的无脊椎宿主建立了共生关系。许多寄生谱系表现出明显不同的身体形态,因此传统上被置于比实际更高的分类等级。最近的一个例子是单型科 Umazuracolidae,它是一种衍生的鱼类寄生虫,具有 bomolochiform 亲缘关系。对属于 21 个镖水蚤科的 44 种的完整 ssrDNA(18S)序列的系统发育分析表明,Umazuracolidae 的家族独特性没有得到支持。最大简约树重建和贝叶斯推断,在核苷酸替代的 GTR+I+Γ 模型下,明确将 Umazuracola elongatus 置于主要鱼类寄生 bomolochiform 复合体中的 Taeniacanthidae 中,驳斥了与多毛类共生体具有共同最近共同祖先的最初建议。系统发育还表明,bomolochiform 科和 Clausidiidae(及其同源)形成一个单系群, Clausidiiform 复合体,在两种方法下都具有高节点支持。贝叶斯推断表明“桡足亚目”的二分起源, Clausidiiform 科家族组处于基础位置,而传统的桡足类科形成一个与第二个桡足亚目分支并列的单系群;然而,最大简约法的结果是模棱两可的,这取决于外群的选择。对单型科 Tegobomolochidae 和 Tuccidae 的形态特征的审查表明,它们只是更具包容性分类群内的衍生谱系,前者与 Bomolochidae 中一组居住在鼻孔中的属有关,后者与 Taeniacanthidae 中的 Taeniacanthodes 形成姐妹群。 Taeniacanthid 属 Makrostrotos 占据 bomolochiform 复合体的基部位置,并被固定为一个新科 Makrostrotidae 的原型。尽管形态和分子证据都表明 Bomolochidae 嵌套在一个并系的 Taeniacanthidae 中,但在没有额外分子数据的情况下,维持这两个科的现状是有利的。包括 Bomolochidae、Taeniacanthidae、Telsidae 和 Makrostrotidae 在内的 bomolochiform 复合体被赋予超科等级,称为 Bomolochoidea。最近对桡足亚目科的一个有争议的系统发育分析被证明是有缺陷的,因为它基于一个包含不完整或误导性信息的数据集,以及其状态被错误评估的特征。