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The subgenus Hystricochaetonotus Schwank, 1990 is one of the most species-rich subgenera of Chaetonotus Ehrenberg, 1830. It has a worldwide distribution and encompasses 37 species predominantly living in the benthos and periphyton of limnetic habitats. We have discovered further nine new species in running and stagnant waters in Slovakia (Central Europe): Ch. (H.) arcanus sp. nov., Ch. (H.) avarus sp. nov., Ch. (H.) gulosus sp. nov., Ch. (H.) iratus sp. nov., Ch. (H.) luxus sp. nov., Ch. (H.) mirabilis sp. nov., Ch. (H.) optabilis sp. nov., Ch. (H.) slavicus sp. nov., and Ch. (H.) superbus sp. nov. Their morphology was studied using differential interference contrast microscopy and subsequent morphometric analyses were carried out. In addition, the primary and secondary structures of their 18S, ITS2, and 28S rRNA molecules as well as their barcoding mitochondrial gene encoding for cytochrome c oxidase (COI) were analyzed. Species boundaries were tested also using the compensatory base change analysis. The new species could be well separated both morphologically and molecularly. The present barcoding analyses revealed that the nuclear ITS2 sequences represent a powerful DNA barcode in addition to the mitochondrial COI gene. According to the multi-gene phylogenetic analyses, the lineage leading to the last common ancestor of the ‘Hystricochaetonotus’ clade is the longest internal branch within the family Chaetonotidae Gosse, 1864. Since members of the subgenus Hystricochaetonotus are morphologically highly heterogeneous, parallel evolution of Chaetonotus-like and/or Hystricochaetonotus-like characters of scales and spines occurred during its radiation.
Four earthworm species, the endogeic Octolasion tyrtaeum (Savigny, 1826), the anecic Lumbricus terrestris Linnaeus, 1758 as well as the epigeic Eisenia fetida (Savigny, 1826) and Dendrobaena veneta (Rosa, 1886), were examined for the presence of astome ciliates. Based on the integrative taxonomic approach, five ciliate species were recognized in their gastrointestinal tracts: Metaradiophrya lumbrici (Dujardin, 1841), M. varians (de Puytorac, 1954), Anoplophrya lumbrici (Schrank, 1803), A. vulgaris de Puytorac, 1954 and A. nodulata (Dujardin, 1841). Their distinctness was assessed using the multivariate morphometric approach and molecular phylogenetic analyses. Although the two species of Metaradiophrya Jankowski, 2007 on the one hand and the two former species of Anoplophrya Stein, 1860 on the other, were not distinctly separated by the multivariate morphometric analyses, they were clearly delimited by the 18S rRNA gene sequences. Species within each genus also differed by their hosts, M. lumbrici and A. lumbrici occurred only in anecic earthworms while M. varians and A. vulgaris occured exclusively in epigeic earthworms. Only a single species, A. nodulata, was detected in endogeic earthworms. It was morphologically distinct from and did not cluster with the two other species of Anoplophrya but was nested within the paraphyletic assemblage containing other astomes from endogeic earthworms. This indicates that the evolution of endosymbiotic ciliates from earthworms has very likely proceeded through a specialization to various ecological groups of their host organisms.
The species of Elmomorphus Sharp, 1888 occurring in Japan and Korea are redescribed and illustrated: E. brevicornis Sharp, 1888 (Japan, Korea) and E. amamiensis Nomura, 1959 (Japan). The standard barcoding fragment of the mitochondrial gene coding for cytochrome c oxidase subunit I (COI) was sequenced and used together with morphological characters to delimit the taxonomic boundaries of the two species. To assess their morphometric variation, eight morphometric characters were measured and statistically evaluated using principal component analysis. The two species of Elmomorphus formed distinct and well-separated clusters in the COI tree. Their interspecific divergence is very high, ranging from 22.7 to 23.9%. On the other hand, morphometric characters, including those previously presumed to be diagnostic, overlap and per se do not allow unambiguous species identification. Reliable morphological distinguishing characters are described for males and females. Molecular data along with the morphological evidence strongly confirm the species status of E. amamiensis. An identification key to the Japanese and Korean species is provided.
Potamophilus kelabitensis sp. nov., a new riffle beetle (Coleoptera, Elmidae) discovered in the Kelabit Highlands (northern Sarawak) and Sapulut environment (southern Sabah), is described. Illustrations of the habitus and diagnostic characters of the new species are presented. Differences from the type species P. acuminatus (Fabricius, 1792) from the Palaearctic region, based on DNA barcodes and morphological characters, are discussed. Selected morphological characters of all known species of Potamophilus from Vietnam, Myanmar, and Papua New Guinea are also compared with the new species. The systematic position of the genus relative to other sympatric genera of the subfamilies Larainae LeConte, 1861 and selected Elminae Curtis, 1830 belonging to three tribes is discussed based on phylogenetic trees inferred from the mitochondrial COI and nuclear ArgK as well as 18S rRNA gene sequences.
The endozoic ciliates of the family Clevelandellidae Kidder, 1938 typically inhabit the hindgut of wood-feeding panesthiine cockroaches. To assess the consistency of species delimitation in clevelandellids, we tested the utility of three sources of taxonomic data: morphometric measurements, cell geometrical information, and 18S rRNA gene sequences. The morphometric and geometrical data delimited the clevelandellid morphospecies consistently and unambiguously. However, only Paraclevelandia brevis Kidder, 1937 represented a homogenous taxon in both morphological and molecular analyses; the morphospecies Clevelandella constricta (Kidder, 1937) and C. hastula (Kidder, 1937) contained two or three distinct, more or less closely related genotypes each; and the genetic homogeneity of the morphospecies C. panesthiae (Kidder, 1937) and C. parapanesthiae (Kidder, 1937) was not corroborated by the 18S rRNA gene sequences at all. Moreover, the 18S rRNA gene phylogenies suggested the C. panesthiae-like morphotype to be the ancestral phenotype from which all other clevelandellid morphotypes arose. The only exception was the C. constricta-like morphotype, which very likely branched off before the diversification of the C. panesthiae-like progenitor. The present molecular analyses also suggested that a huge proportion of the clevelandellid diversity still waits to be discovered, since examination of only four panesthiine populations revealed 10 distinct clevelandellid genotypes/molecular species.