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EDUARDO MATEOS amp; PENELOPE GREENSLADE (2021) Towards understanding Lepidocyrtus Bourlet, 1839 (Collembola, Entomobryidae) II: new Australian species, Zootaxa, 4981: 365387

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The Collembolan genus Lepidocyrtus is subdivided into up to eight subgenera, of which only Lepidocyrtus s.str. (Bourlet, 1839) and Lanocyrtus (Yoshii & Suhardjono, 1989) are represented by European species. The discovery of unique characters in the European species Lepidocyrtus tomosvaryi (rounded dental tubercle) and L. peisonis (lateral tuft of long filiform chaetae in abdomen III) has only described so far for species of the subgenera Setogaster (Salmon, 1951) and Cinctocyrtus (Yoshii & Suhardjono, 1989) and has raised the need to perform a molecular analysis by involving other representative species of the genus. For this study, phylogenetic analysis of 15 Lepidocyrtus species occurring in the Carpathian Basin were carried out. The analyses, which was based on both concatenated datasets of COII and EF1-α sequences and individual gene sequences, clearly placed L. tomosvaryi within the subgenus Lanocyrtus and L. peisonis within Lepidocyrtus s.srt. European species groups defined on the basis of morphological characters were only partly confirmed by the concatenated and COII analyses because of the splitting of the pallidus–serbicus-group, whereas EF1- α sequences weakly supported this group.
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The largest superfamily Entomobryoidea is one of the key groups in Collembola. However, incorrect recognition of chaetotaxic homology within Entomobryoidea severely impedes the accurate species comparison of adults and phylogenetic reconstruction. Traditional classification of the superfamily at suprageneric level is disputable in the light of recent advances. Transformational homology of tergal chaetotaxy was traced and revised based on 38 species of first instar and partial early instars. Morphological phylogenetic reconstructions were reconstructed mainly relying on first instar characters using both parsimony and likelihood-based algorithms. Outgroup selection and several rogue taxa impacted on resolution and support of otherwise well-supported clades. Integrating published molecular phylogeny, a revised classification of three families and nine subfamilies was presented: Orchesellidae, Entomobryidae and Paronellidae. Orchesellidae includes all basal taxa having a short fourth abdominal segment. Cyphoderidae and Microfalculidae taxa were sunk into Paronellidae. New Paronellidae was divided into two subfamilies: Paronellinae (Paronellini + Cyphoderini + Bromacanthini) and Salininae (Cremastocephalini + Callyntrurini). Microfalculidae (Microfalcula) was closer to Salina and Akabosia and thus transferred into Cremastocephalini. This study erected a new classification framework for Entomobryoidea based upon comprehensive phylogenies. Chaetotaxic homologization across a wide range provided a standardized, comparable, powerful tool for taxonomy.
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The present contribution gives a taxonomic account of the members of the springtail genus Pseudosinella Schäffer, collected during the 2004–2006 expeditions organized by Daniel Fong and David Culver to caves of eastern and southern West Virginia. These expeditions are part of an ongoing long-term effort to develop a complete inventory of the cave fauna of the state. The samples examined include seven species of Pseudosinella, two of which, P. josemarii sp. nov. and P. meganporteri sp. nov. are new to science. For five previously named species descriptive notes are given emphasizing new or incompletely described characters such as the dorsal and ventral head chaetotaxy, number of teeth in the ungulum of the maxilla, presence or absence of setae a6 on the first abdominal segment, and lateral chaetotaxy of the fourth abdominal segment. Detailed analysis of the dorsal chaetotaxy of the head shows that Gisin's RST system of nomenclature confounds the identity of some macrosetae, hence, a new nomenclature system, denominated AMS, is proposed to more consistently identify macrosetae across all Lepidocyrtini. In addition, a system is proposed to describe variation in number of postlabial setae, their shape and ornamentation.
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The correct identification of morphological species is a key task for species richness estimation of any ecosystem. Although body colour is a widely used character identifying European Lepidocyrtus species, recent investigations using molecular data have revealed that species delineation using body colour can result in an underestimation of real species diversity because of the presence of cryptic species. Lepidocyrtus violaceus is a European species characterised by its dark violet body colour. Its wide distribution leads us to suspect that several cryptic species can be present within this morphospecies. Since traditional morphological characters have appeared insufficient for real diversity identification in Lepidocyrtus, new morphological characters were needed in order to describe the cryptic diversity detected by molecular data in this genus. Pseudopores are integumentary structures present in all Lepidocyrtus species, but the distribution of these structures has not been properly described in the genus, as well as in Entomobryioidea overall. In the present work we aimed to analyse whether L. violaceus is a monophyletic entity in Europe. Moreover, we aimed to determine if the position and number of pseudopores on the different parts of the body and appendages is a phylogenetically useful character in the identification of the species or superspecific entities. Fourteen populations of L. violaceus from five European countries, and another 25 Lepidocyrtus species from nine European countries have been studied. In total, 208 specimens have been analysed morphologically and half of them were studied molecularly using sequences of the genes COXII and EF-1α. Molecular data revealed that the widely distributed Lepidocyrtus violaceus morphospecies is a polyphyletic entity in Europe. Between 6 and 12 diferent cryptic species have been detected within this European morphospecies, and only the presence of pseudopores on the basal plate of the fourth abdominal segment has been found to be a promising diagnostic character between them. A common basal pattern of pseudopore distribution has been recognised in the European members of the genus, and also a diferential pattern within each European species group. As a general trend, an increase in the number of pseudopores has been detected from the most basal to the most derived species groups in the phylogeny of the genus in Europe.
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Collembola are an important component of montane arthropod communities worldwide, where they are often the most abundant and active group. In Australia, montane ecosystems are predicted to contract with continued climate warming, yet little is known about the faunal composition of Collembola on mountains nor its level of endemism. We compared the composition of Collembola communities from five mountain summits along a latitudinal gradient in eastern Australia. Each mountain harboured a distinct Collembola community, with few shared species/morphospecies. Even at the genus and family level, however, mountains varied considerably in faunal composition. Although no latitudinal trends were detected, short range endemism of morphospecies was high. Year-to-year variation in community composition within sites was small compared to between-site variation, even when collections were made 10 years apart. These results suggest that montane Collembola taxa may be resilient, as far as short term variations in weather are concerned. However, there is no evidence as to whether longer-lasting warmer conditions would be tolerated. If not, large scale losses of locally endemic species but not genera, unless they are monobasic, are likely.
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Twelve species of Lepidocyrtus and 2 species of Pseudosinella are described. -from Author
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Entomobryidae, the largest collembolan family, is traditionally classified at suprageneric level using a limited set of morphological structures, such as scales, antennal segmentation. Most tribal and subfamilial delimitations appear, however, disputable in the light of recent works. Integrating molecular and morphological evidence, we propose here a revision of the systematics of the family. In addition to traditional taxonomic characters, tergal specialized chaetae (S-chaetae) are newly introduced, and their patterns are shown to be diversified at all levels from species to subfamilies. S-chaetotaxic pattern on phylogenetic tree shows that evolution of S-chaetae is not parallel between the different terga and that their patterns coincide well with the known molecular phylogeny, providing a powerful tool for the systematics of Entomobryidae. Orchesellinae sensu Soto-Adames et al. (Annals of the Entomological Society of America, 101, 2008, 501); is divided into three subfamilies: Orchesellinae s. s., Bessoniellinae and Heteromurinae, the latter two upgraded from the original tribal level. Entomobryinae sensu Szeptycki (Morpho-Systematic Studies on Collembola. IV. Chaetotaxy of the Entomobryidae and its Phylogenetical Significance, 1979), is no longer divided into scaled and unscaled tribes, and Lepidosira-group is transferred from Seirinae to Entomobryinae. A key to subfamilies and tribes and a comparison with previous classifications of the Entomobryidae are provided. This study greatly improves the understanding of primary and secondary characters and erects the fundamental framework for the taxonomy of Entomobryidae.
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We examined and keyed out the subgenera of the genus Lepidocyrtus mostly created by Yoshii. Although many of these subgenera of the genus Lepidocyrtus are difficult to apply in Europe, America, and Africa, they are easily applicable in East and Southeast Asia. The species of Southeast Asia are placed in these subgenera and a key to the subgenera is provided. A new species, Lepidocyrtus (Lanocyrtus) felpei from Xinjiang, People's Republic of China, is described and the species Lepidocyrtus (Lanocyrtus) fimetarius Gisin is redescribed. Although the Lepidocyrtus fauna of the whole of East Asia differs from the Holarctic fauna, the Central and Northeast Asian fauna are similar in subgeneric make up to the North American fauna, slightly less similar to the European fauna, and totally unlike the Southeast Asian fauna.
Article
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