Registered users receive a variety of benefits including the ability to customize email alerts, create favorite journals list, and save searches.
Please note that a BioOne web account does not automatically grant access to full-text content. An institutional or society member subscription is required to view non-Open Access content.
Contact helpdesk@bioone.org with any questions.
Morphology still plays a key role in the systematics and phylogenetics of most of the scorpion families and genera, including the Diplocentridae Karsch, 1880. The monophyly of this family, and the monophyly of its two subfamilies is supported by morphological characters; however, neither hypothesis has been tested using molecular data. The lack of a molecular phylogeny has prevented the study of the evolution of morphology within the family. Here, we examine the morphological evolution of several key character systems in diplocentrid systematics. We tested the monophyly of the Diplocentridae, and subsequently the validity of its two subfamilies using a five-locus phylogeny. We examined the variation and evolution of the shape of the carapace, the external surface of the pedipalp patella and the retrolateral surface of the pedipalp chelae of males and females. We also examined the phylogenetic signal of discrete and continuous characters previously reported. We show that Diplocentridae is monophyletic, but Nebinae is nested within Diplocentrinae. Therefore, Nebinae is synonymised with Diplocentrinae (new synonymy). Finally, we show that a new character system proposed here, tarsal spiniform and macrosetal counts, retains high phylogenetic signal and circumscribes independently evolving substructures within this character system.
The systematics of Semisulcospiridae in Korea is critically revised by means of comparative anatomy, including comprehensive review of type material and mitochondrial phylogenetics (sequences of COI and 16S). The family is represented by two genera with different reproductive modes: Semisulcospira Boettger, 1886 is viviparous and contains three species (S. coreana (Martens, 1886), S. gottschei (Martens, 1886) and S. forticosta (Martens, 1886)) while Koreoleptoxis Burch & Jung, 1988 is oviparous and also contains three species (K. globus (Martens, 1886), K. nodifila (Martens, 1886), K. tegulata (Martens, 1894)). Koreanomelania Burch & Jung, 1988 is synonymised with Koreoleptoxis. Species can be distinguished by differences in shell shape and sculpture. They form well-differentiated clusters in the mitochondrial phylogeny, consistently revealing lower intraspecific than interspecific genetic distances. Sequences of Japanese Semisulcospira species fall into three distinct major clades (A–C), rendering Semisulcospira non-monophyletic in the mitochondrial tree. Only a small number of Japanese samples were closely related to the Korean clade (Clade C). The numerically predominant Japanese mitochondrial Clade B exhibited increased lineage divergence and, when translated into amino acids, significantly more amino acid substitutions in comparison with Korean species. I conclude that these Japanese sequences may be paralogous and/or may undergo non-neutral evolution. Hence, they are not suitable for inferring phylogenetic relationships.
This study forms a major step towards a comprehensive morphological and molecular analysis of the species diversity of European microplanid land planarians. It presents a molecular phylogenetic tree on the basis of information from the genes Cox1, 18S, 28S and elongation factor 1-α, and applies molecular and morphological species delimitation methodologies for Microplana specimens sampled over a wide geographic range within Europe. The study suggests that as yet there is no plateau or asymptote in the accumulation curve for European Microplana species, as our results facilitated an integrative delimitation of seven new species as well as the diagnosis of new populations of three already known species and one doubtful or problematic species. In some cases, the new records considerably enlarged the known range of a species. An integrative account is provided of each of these species. Molecular sequence information on newly collected land flatworms may quickly point the planarian systematist to taxa that need to be examined morphologically and thus may considerably reduce laborious and time-consuming histological analyses.
A dated molecular phylogeny is proposed for the Tanypodinae, a diverse subfamily of Chironomidae (Diptera). We used molecular data from fragments of one ribosomal gene (28S), one nuclear protein-coding gene (CAD), and one mitochondrial protein-coding gene (COI), analysed using mixed model Bayesian and maximum likelihood inference methods. All proposed tribes were sampled, namely, Anatopyniini, Clinotanypodini, Coelopyniini, Fittkauimyiini, Macropelopiini, Natarsiini, Pentaneurini, Procladiini and Tanypodini. A multilocus dataset of 1938 characters was compiled from 123 individuals including outgroups. Monophyly was supported for all tribes although some relationships were not robust. Relationships between tribes and some genus groups are highly congruent with a morphology-based estimate. Relationships within tribe Pentaneurini mostly find weak support, yet previously hypothesised groupings and monophyly or lack thereof in well-sampled genera are revealed. The tempo of diversification of the family was deduced by divergence time analysis (BEAST). Origination of a subfamily stem group in the late Jurassic to early Cretaceous was inferred, with all tribes and many genera of Pentaneurini originating and diversifying in the Cretaceous. Some nodes are biogeographically informative. Gene sections supported the backbone, but more extensive sampling is needed to estimate shallower phylogenies and to better understand the tempo and diversification of Tanypodinae.
Systematic relationships among Laniatores have received considerable attention during the past few years. Many significant taxonomic changes have been proposed, particularly in the superfamily Gonyleptoidea. As part of this superfamily, the basalmost Stygnopsidae is the least known family. In order to propose the first total evidence phylogeny of the family, we produced four datasets: three molecular markers – partial nuclear 28S, mitochondrial ribosomal 16S, mitochondrial protein-encoding cytochrome c oxidase subunit I; and 72 morphological characters. With these data, we performed three different phylogenetic analyses: (1) Bayesian Inference with molecular data, and (2) Bayesian Inference and (3) Maximum Likelihood using combined data. Our results are congruent: a monophyletic Stygnopsidae subdivided into two major clades: Stygnopsinae and Karosinae, subfam. nov. The following genera are redefined: Stygnopsis, Hoplobunus and Serrobunus stat. rev. The following taxa are described: Iztlina venefica, gen. nov., sp. nov. and Tonalteca, gen. nov. Additionally, the following changes are proposed: Serrobunus queretarius (Šilhavý, 1974), comb. nov., Stygnopsis apoalensis (Goodnight & Goodnight, 1973), comb. nov., Stygnopsis mexicana (Roewer, 1915), comb. nov., Stygnopsis oaxacensis (Goodnight & Goodnight, 1973), comb. nov., and Tonalteca spinooculorum (Goodnight & Goodnight, 1973), comb. nov. We also discuss the status of the genera Isaeus stat. rev. and Mexotroglinus. Finally, we discuss the evolution of male genitalia and convergence of selected homoplastic diagnostic characters.
On p. 251, line 10, the in-text table citation should be ‘Table S1’ so that the sentence reads as ‘All new sequences have been deposited with GenBank (Table S1).’
This article is only available to subscribers. It is not available for individual sale.
Access to the requested content is limited to institutions that have
purchased or subscribe to this BioOne eBook Collection. You are receiving
this notice because your organization may not have this eBook access.*
*Shibboleth/Open Athens users-please
sign in
to access your institution's subscriptions.
Additional information about institution subscriptions can be foundhere