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.

Among Opiliones (Arachnida), there are many taxa either with no familial assignment or erroneously located in their current family. This is the case of Ethobunus pilosus, formerly in Phalangodidae and before this work in Zalmoxidae. To assess the phylogenetic position of this taxon, we started with a revision of the male genitalia; followed by the inclusion of three molecular markers: nuclear 28S and 18S, and mitochondrial protein-encoding cytochrome c oxidase subunit I (COI) from E. pilosus in the previously published phylogenies of the Samooidea + Zalmoxoidea clade. The results revealed that E. pilosus is a derived lineage within the family Icaleptidae, thus it is transferred from Zalmoxidae, and the new name Trypophobica gen. nov. is proposed to accommodate it, with the new combination Trypophobica pilosa comb. nov. With its inclusion in Icaleptidae, and the description of Trypophobica llama sp. nov., the current diagnosis of the family needs updating, and further morphological characters should be considered as putative synapomorphies. In addition, the reconstruction of the ancestral ranges of Icaleptidae suggests a mid-Cretaceous origin c. 104 Ma in South America, with a subsequent colonisation to north Mesoamerica c. 80 Ma.

The Australian golden trapdoor spiders of the tribe Euoplini (family Idiopidae) are among the most abundant and diverse of mygalomorph lineages in subtropical eastern Australia. Throughout this highly populated area, species in the monophyletic Euoplos variabilis-group are largely ubiquitous; however, species delimitation has long proven difficult in the group because species are morphologically very similar and have parapatric or even sympatric distributions. We address these challenges in the variabilis-group, and explore the phylogeny and taxonomy of species using an integrative systematic approach. In doing so, we apply a conservative, pragmatic methodology, naming only species for which adequate data are available (namely sequence data and unequivocally linked male specimens), and explicitly stating and mapping material that could not be linked to a species, to aid future research on the group. We describe five new species from south-eastern Queensland –E. booloumba sp. nov., E. jayneae sp. nov., E. raveni sp. nov., E. regalis sp. nov. and E. schmidti sp. nov.; we redescribe two previously named species – E. similaris (Rainbow & Pulleine, 1918) and E. variabilis (Rainbow & Pulleine, 1918); and we reillustrate the recently described E. grandis Wilson & Rix, 2019. The nominate species, E. variabilis, is shown to have a far smaller distribution than previously thought, and E. similaris is given a modern taxonomic description for the first time. A key to adult male specimens is also provided. This study further reveals a case of sympatry between two species within the variabilis-group; both E. raveni sp. nov. and E. schmidti sp. nov. occur in the Brisbane Valley, south of the Brisbane River – a notable result given that closely related mygalomorph species usually occur allopatrically. This work updates what is currently known of the phylogeny and diversity of one of the dominant mygalomorph lineages of subtropical eastern Australia, resolving a complex and highly endemic fauna.

Some brachyuran crab species of the Western Pacific appear to be widespread throughout the region and distributed across a large geographic area, without obvious phylogeographic structuring. In the present study, we describe a new species of Parasesarma that appears to be restricted to Western Pacific islands (so far Guam, Palau, Vanuatu, Fiji, Wallis and New Caledonia). Comparisons of partial sequences of the COX1 gene show that individuals of this species, though from relatively isolated and widely separated islands, are monophyletic and, surprisingly, genetically uniform. These results give credence to the hypothesis that these oceanic islands serve as ‘stepping stones’ for the current-mediated dispersal and genetic homogenisation of coastal–littoral marine species. Morphologically, the new species differs most significantly from similar congeners in the tuberculation pattern of the chelar dactyli, whereas genetically it is markedly divergent from other morphologically similar species of Parasesarma, with a minimum COX1 p-distance of 6.9%. With such evidence, the new species is here formally described as Parasesarma daviei sp. nov. It is the fifth species of Parasesarma reported from oceanic islands of the Western Pacific. Compared to other congeners, P. daviei sp. nov. shows a close relationship with a clade including P. calypso. Therefore, P. calypso (De Man, 1895), and three of its former subspecies or varieties were subjected to a closer examination and are here rediagnosed and illustrated. In consequence, we suggest full species status for P. kuekenthali (De Man, 1902), P. lanchesteri (Tweedie, 1936), and P. ellenae (Pretzmann, 1968).

The cicadas (Hemiptera: Cicadidae) related to tribe Cicadini exhibit some of the most remarkable phenotypes in the family, with many genera possessing striking colour patterns and unusual morphological features. This largely Asian group of 13 tribes has proven challenging for cicada taxonomists, in part because of likely convergent evolution or losses of these phenotypes. We present the first focused molecular phylogeny of this clade, including ∼60 described genera. The genetic dataset contains 839 ingroup-informative sites (out of 2575) from mitochondrial cytochrome c oxidase subunit I, nuclear elongation factor-1 α, and nuclear acetyltransferase. We use Bayesian and maximum likelihood trees to test recent changes in tribe- and subtribe-level classification, and we reconstruct ancestral character states for potentially convergent traits influencing tribe descriptions. We use fossil and molecular clock calibrations to estimate the temporal and geographic context of the radiation. The tribes Gaeanini, Leptopsaltriini, Platypleurini, Psithyristriini, and Tosenini appear polyphyletic and in need of revision, in part because of convergent evolution of opaque wings and multiple convergent gains or losses of abdominal tubercles. Kalabita Moulton, 1923 is transferred from Platypleurini to Leptopsaltriini. Vittagaeana gen. nov. is established for Vittagaeana paviei comb. nov. and Vittagaeana dives comb. nov., formerly in Tosena. Sinosenini syn. nov. is synonymised with Dundubiina. Ayuthiini trib. nov. is established with two new subtribes for Ayuthia Distant, 1919 and Distantalna Boulard, 2009, formerly in Tosenini. For the earliest split in the tree, one common ancestor appears to have been Indian + Asian in geographic distribution and the other Asian. We estimate that the radiation began in the middle Cenozoic Era, possibly as recently as the early Miocene. The recent and steady pattern of diversification suggests that refinement of tribe diagnoses will prove challenging.