Article

Discovery of two new Diaulota Casey species (Coleoptera: Staphylinidae: Aleocharinae) from coastal Hokkaido, Japan based on morphological and molecular characters

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  • Research Center for Endangered Species - National Institute of Ecology
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Abstract

Diaulota hokkaidona Ahn and Ôhara, sp. n. and Diaulota oharai Ahn and Yoo, sp. n. are described from coastal Hokkaido, Japan. Diaulota hokkaidona Ahn and Ôhara, sp. n. is very similar to D. aokii Sawada and cannot be distinguished by the external morphological characters but they are separated by the structures of median lobe of aedeagus and molecular characters (COI). They can be regarded as cryptic species. The minimum interspecific difference between Diaulota aokii and Diaulota hokkaidona Ahn and Ôhara, sp. n. (6.7%) was much higher than the maximum intraspecific difference of Diaulota hokkaidona Ahn and Ôhara, sp. n. (0.7%) and they contained 17 and 13 molecular diagnostic characters, respectively. The molecular analyses support the validity of two new species based on morphological characters. A revised key is provided for separation of the known species of Diaulota Casey, and descriptions with illustrations of diagnostic features of two new species are presented.

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... Japanese species of this tribe have been extensively studied (e.g., Sawada, 1971Sawada, , 1991Ono & Maruyama, 2014;Song et al., 2018). However, some of Dr. Kohei Sawada's described species, namely Diaulota aokii, D. pacifica and Amblopusa pacifica, were subsequently redescribed without reference to Japanese specimens, leading to misidentifications (Ahn & Ashe, 1995;Ahn, 1996Ahn, , 2023. ...
... Recently, Song et al. (2018) described a species, D. hokkaidona previously considered as "D. aokii" from Hokkaidô, Alaska, and Kamchatka, so the true D. aokii was considered to be distributed in Honshû and Korea. ...
... The representation of the Korean "D. aokii" in Ahn (1996) and Song et al., (2018) is likely a result of misidentification. Given that recent phylogenetic investigations (Ahn & Ashe, 1996b;Ahn et al., 2010;Song et al., 2018;Yoo & Ahn, 2021) were founded on this erroneous identification, it is imperative to conduct further analyses of Diaulota based on the accurate identification. ...
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Japanese fauna of the intertidal rove beetle of tribe Liparocephalini Fenyes, 1918 is reviewed and six genera and 26 species are recognized. A new genus, Rotundicephala Tasaku, Ono & Maruyama, gen. n., is described to include R. pacifica (Sawada, 1971) comb. n. (type species; transferred from Diaulota), R. koreana (Yoo & Ahn, 2021), comb. n. (transferred from Diaulota) and R. koheii Tasaku, Ono & Maruyama, sp. n. Four new species are described: Diaulota decipiens Tasaku, Ono & Maruyama, sp. n., which has been confused with “D. aokii”, D. orientalis Tasaku, Ono & Maruyama, sp. n., R. koheii Tasaku, Ono & Maruyama, sp. n., and Paramblopusa sumikawai Tasaku, Ono & Maruyama, sp. n. Three species, Amblopusa brevipes Casey, 1893, D. submarina Ahn, 2023 and R. koreana, are reported from Japan for the first time. We provide keys to genera and species, illustrations of mouth parts and diagnostic characteristics of each genus, and diagnostic characteristics and illustrations of the genitalia of almost all species. Biogeographical patterns of Diaulota and Rotundicephala gen. n., and the tribal range and monophyly of Liparocephalini are discussed. Three genus-group: the Liparocephalus genus-group, the Amblopusa genus-group, and the Paramblopusa genus-group are recognized in the tribe, but Baeostethus Broun, 1909 known from New Zealand is regarded as incertae sedis. The genera Ashella Klimaszewski, 2020 and Ianmoorea Ahn, 2006 are excluded from Liparocephalini.
... The intertidal genus Diaulota Casey contains 11 species and occurs on the rocky shores along the Pacific coasts of Northern hemisphere (Frank and Ahn, 2011). Since the genus was established by Casey (1893), they were revised (Ahn, 1996) and three additional species were described on the East Asian coasts (Song et al., 2018;Yoo and Ahn, 2021). Song et al. (2018) suggested that D. aokii Sawada and D. hokkaidona Ahn and Ôhara were cryptic species. ...
... Since the genus was established by Casey (1893), they were revised (Ahn, 1996) and three additional species were described on the East Asian coasts (Song et al., 2018;Yoo and Ahn, 2021). Song et al. (2018) suggested that D. aokii Sawada and D. hokkaidona Ahn and Ôhara were cryptic species. While working on the phylogeny of Diaulota, I recognized that there were two lineages, each with a long branch within D. uenoi (Sawada) clade, which implied that there might be cryptic species (unpublished data). ...
... Terms used here generally followed Sawada (1972), but I followed Ashe (1984) in some cases, especially for the aedeagus and mouthparts. Key to the species of Diaulota from the world (Updated and revised from Ahn, 1996;Song et al., 2018;Yoo and Ahn, 2021. Note that dissections of the male genitalia are essential for correct species identification.) ...
Article
Taxonomy of the intertidal Diaulota Casey is briefly reviewed and 12 species are listed including a new species. Diaulota submarina sp. nov. is described with illustrations of diagnostic characters and a revised key to the species of Diaulota is provided. The new species is remarkably similar to D. uenoi (Sawada) and indistinguishable by external morphological characters. They can be regarded as cryptic species.
... Liparocephalini Fenyes containing 33 species in seven genera worldwide are confined to intertidal habitats along the Pacific coasts (Ahn and Frank, 2011;Ono and Maruyama, 2014;Ahn, 2017, 2020;Song et al., 2018). They have been known as a monophyletic lineage based on the following synapomorphies: seta v absent on mentum, one medial seta present on prementum, contiguous mesocoxal cavities, and galea with several setae only on mesal surface and apex with setae (Ahn, 2004;Ahn et al., 2010). ...
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Diaulota koreana Yoo and Ahn new species is described in the intertidal zones of the southern part of the Korean peninsula and illustrations of diagnostic characters are presented. A cladistic analysis of the Liparocephalini based on 50 adult characters suggests that the new species belongs to the genus Diaulota Casey within the Liparocephalini. Similarities and differences among the liparocephaline genera are presented. Phylogenetic relationships of Diaulota koreana Yoo and Ahn new species among the Liparocephalini are briefly discussed.
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A phylogenetic analysis of the tribe Liparocephalini Fenyes is presented based on morphological and molecular characters. The data set comprised 50 adult morphological characters, partial COI (907 bp), COII (366 bp) and 12S rDNA (325–355 bp), and nearly complete sequences of 18S rDNA (1768–1902 bp) for 21 species. Eighteen species of liparocephaline beetles from all eight genera and three outgroups, are included. The sequences were analysed separately and simultaneously with morphological characters by direct optimization in the program POY4 and by partitioned Bayesian analysis for the combined data. The direct optimization (DO) tree for the combined data under equal weighting, which also shows a minimum incongruence length difference value, resulted in a monophyletic Liparocephalini with the following patterns of phylogenetic relationships (outgroup ((Baeostethus, Ianmoorea) (Paramblopusa ((Amblopusa, Halorhadinus) (Liparocephalus, Diaulota))))). A sensitivity analysis using 16 different parameter sets for the combined data shows the monophyly of the liparocephalines and all its genera under all parameter sets. Bayesian analysis resulted in topological differences in comparison with the DO tree under equal weighting only in the position of the genus Paramblopusa and clade (Amblopusa + Halorhadinus), which were reversed. Historical biogeography and the stepwise evolutionary colonization of intertidal habitat in the Liparocephalini are discussed. Based on the biogeographical analyses, we hypothesize that the ancestor of the Liparocephalini occurred along the Panthallassan Ocean, the direct antecedent of the Pacific Ocean, followed by repeated dispersals to the Nearctic from the Palearctic. We also hypothesize that ancestors of the Liparocephalini appear to have arisen in the littoral zone of beaches and then colonized rocky reef areas in the low tidal zone later through high- to mid-tide zones. © The Willi Hennig Society 2009.
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Some simple formulae were obtained which enable us to estimate evolutionary distances in terms of the number of nucleotide substitutions (and, also, the evolutionary rates when the divergence times are known). In comparing a pair of nucleotide sequences, we distinguish two types of differences; if homologous sites are occupied by different nucleotide bases but both are purines or both pyrimidines, the difference is called type I (or "transition" type), while, if one of the two is a purine and the other is a pyrimidine, the difference is called type II (or "transversion" type). Letting P and Q be respectively the fractions of nucleotide sites showing type I and type II differences between two sequences compared, then the evolutionary distance per site is K = -(1/2) ln [(1-2P-Q) square root of 1-2Q]. The evolutionary rate per year is then given by k = K/(2T), where T is the time since the divergence of the two sequences. If only the third codon positions are compared, the synonymous component of the evolutionary base substitutions per site is estimated by K'S = -(1/2) ln (1-2P-Q). Also, formulae for standard errors were obtained. Some examples were worked out using reported globin sequences to show that synonymous substitutions occur at much higher rates than amino acid-altering substitutions in evolution.
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We investigated the phylogenetic relationships of carrion beetles (Coleoptera, Silphidae) using 2094 bp of their mitochondrial cytochrome oxidase subunit I and II and tRNA leucine gene sequences. Shorter fragments of this gene region previously have been used to establish generic relationships in insects. In this study, they provided more than sufficient resolution, although the third positions of the protein-coding sequences reached saturation for the deeper divergences. This first published phylogeny for the Silphidae comprises 23 species from 13 genera sampled across the geographic range of the family. In addition, we included species from three related families as outgroups. One of these families, the Agyrtidae, was, until recently, included in the Silphidae, but its resolution here justifies its current position as a separate family. The silphid subfamilies Nicrophorinae and Silphinae are monophyletic in all analyses. All genera for which several species were sampled are supported as monophyletic groups, with the exception of the genus Silpha. European and North American representatives of two Nicrophorus species described from both continents are supported as each others' closest relatives. The lineage that colonized Gondwanaland and that most likely originated in the Palearctic is the most basal within the Silphinae.
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Jones, T.W., 1968. The zonal distribution of three species of Staphylinidae in the rocky intertidal zone in California (Coleoptera: Staphylinidae). Pan-Pac. Entomol. 44, 203-210.
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Generic revision of the subtribe Gyrophaenina (Coleoptera: Staphylinidae: Aleocharinae) with a review of the described subgenera and major features of evolution
  • Ashe
Ashe, J.S., 1984. Generic revision of the subtribe Gyrophaenina (Coleoptera: Staphylinidae: Aleocharinae) with a review of the described subgenera and major features of evolution. Quaestiones Entomologicae 20, 129-349.
When rare species become endangered: cryptic speciation in myrmecophilous hoverflies
  • Schönrogge
XII. Subfamily Aleocharinae Fleming 1821
  • Ashe