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Australia is predicted to have a high number of currently undescribed ostracod taxa. The genus Bennelongia De Deckker & McKenzie, 1981 (Crustacea, Ostracoda) occurs in Australia and New Zealand, and has recently shown potential for high speciosity, after the description of nine new species from Western Australia. Here, we focus on Bennelongia from eastern Australia, with the objectives of exploring likely habitats for undiscovered species, genetically characterising published morphological species and scanning classical species for cryptic diversity. Two traditional (morphological) species are confi rmed to be valid using molecular evidence (B. harpago De Deckker & McKenzie, 1981 and B. pinpi De Deckker, 1981), while three new species are described using both morphological and molecular evidence. Two of the new species belong to the B. barangaroo lineage (B. dedeckkeri sp. nov. and B. mckenziei sp. nov.), while the third is a member of the B. nimala lineage (B. regina sp. nov.). Another species was found to be genetically distinct, but is not formally described here owing to a lack of distinguishing morphological features from the existing species B. cuensis Martens et al., 2012. Trends in diversity and radiation of the genus are discussed, as well as implications these results have for the conservation of temporary pool microfauna and our understanding of Bennelongia’s evolutionary origin.
The Western Ghats of India is considered one of the richest biodiversity hotspots in the world. Documenting scorpion diversity has always been of paramount importance due to their species richness, ecological role and endemism, which calls for conservation priority. Scorpion diversity of the Western Ghats is probably underestimated given the ancestry of the group, and more field work in the region is very likely to uncover numerous undescribed taxa. Several new Indian species have recently been discovered in the scorpion genus Isometrus Ehrenberg, 1828 (Scorpiones: Buthidae). In this communication, we resurrect I. sankeriensis Tikader & Bastawade, 1983 and describe two new species from the Western Ghats of India, I. nakshatra sp. nov. and I. wayanadensis sp. nov., using an integrative taxonomic approach. In order to replace the lost holotype of I. sankeriensis, we designate a neotype and reassess the identity of this species. This work elevates the number of species of Isometrus found in India to eight and we expect many more scorpion discoveries from India with continued research.
The Asplenium coenobiale complex is distributed in Eastern Asia and Southeast Asia with its distribution center in southwestern China. In this study, we carried out a detailed morphological, cytological, and phylogenetic study by adding two samples from Danxia landform in Guangdong. The sequences of five chloroplast markers and one nuclear marker of the A. coenobiale complex were analyzed with maximum likelihood and Bayesian inference, respectively. The morphological and phylogenetic analyses support the recognition of a new species (A. danxiaense K.W.Xu sp. nov.) of the A. coenobiale complex from a cave of Danxia mountain, Guangdong province, southern China. This new species can be distinguished from A. coenobiale and A. pulcherrimum by having scales narrowly triangular to lanceolate, apex ending in a short apical tail, basal basiscopic pinnule usually largest, fertile segment scarce, and exospore length usually more than 50 μm and shows significant molecular differences from other species in this complex. A detailed description and illustrations are presented.
Initial analyses of DNA barcode data from Norwegian populations attributed to the water mite Lebertia porosa Thor, 1900 revealed large genetic divergence and potentially cryptic species-level diversity. We used one mitochondrial (COI) and two nuclear markers (18S and 28S) as well as comparative morphological analysis to redefine Lebertia porosa, and to further investigate the species boundaries of Norwegian populations of its close relatives. Our results show that Lebertia porosa, as currently defined, consists of multiple species that can be separated by molecular and morphological characteristics. Although we document the presence of the endosymbiotic bacteria Wolbachia in two out of eight screened genetic lineages, we find no evidence of intraspecific genetic divergence caused by Wolbachia infections. The assignment of one of the genetic lineages to the nominal species could be made through morphological comparisons of specimens from the L. porosa type locality with the syntypes of L. obscura Thor, 1900. Thus, the diagnosis of L. porosa is emended and a neotype is defined. Two of the remaining genetic lineages could be assigned to existing names previously regarded as junior synonyms of L. porosa, namely L. obscura (lectotype defined here) and L. gibbosa Lundblad, 1926, which are both redescribed. The outstanding genetic lineages are unnamed, but from our work we conclude that the taxa Lebertia porosa britannica Thor, 1906, L. porosa dorsalis Thor, 1906, and L. porosa italica Thor, 1906 are nomina dubia that cannot be considered junior synonyms of L. porosa as proposed by K. Viets (1956). We also consider L. vigintimaculata Thor, 1900 a nomen dubium, probably identical to L. obscura.
Morphological and allozyme analyses suggested the occurrence of a pseudocryptic species in the Lasioglossum villosulum (Kirby, 1802) species complex (Hymenoptera: Halictidae). We analysed the morphology of more than 1500 specimens and the DNA barcode fragment of the cytochrome c oxidase subunit I (COI) of 102 specimens of this species complex from several Palaearctic countries. Our phylogenetic tree reconstructions, based on maximum likelihood and Bayesian inference revealed one clade corresponding to all specimens morphologically identified as Lasioglossum medinai (Vachal, 1895) and one divergent specimen morphologically identified as Lasioglossum berberum (Benoist, 1941). The other specimens, morphologically identified as L. villosulum, aggregated into at least three other lineages in our phylogenetic trees. The tree-based species delineations methods based on the Generalized Mixed Yule Coalescent (GMYC) model and the Bayesian Poisson Tree Process (bPTP) identified five to ten candidate species within the L. villosulum species complex, with L. medinai and L. berberum consistently recognized as separated from all other candidate species. Diagnostic morphological differences were found among L. medinai, L. berberum and the remaining specimens identified as L. villosulum. No diagnostic morphological differences were found to distinguish the different phylogenetic candidate species or lineages found within L. villosulum and L. medinai. Thus, both genetic and morphological approaches support the existence of L. medinai and L. berberum as distinct species from L. villosulum.
Large ants are not easy – the taxonomy of Dinoponera Roger (Hymenoptera: Formicidae: Ponerinae)
(2021)
The taxonomy of the giant ants of the genus Dinoponera is revised based on female and male morphology. Eight species are recognized. Dinoponera nicinha sp. nov., from Amazonas and Rondônia, Brazil, is described and D. grandis (Guérin-Méneville, 1838) is revived. The species D. australis Emery, 1901 and D. snellingi Lenhart, Dash & Mackay, 2013, plus the subspecies D. australis bucki Borgmeier, 1937 and D. australis nigricolor Borgmeier, 1937 are synonymized under D. grandis sp. rev. An unnamed and unidentified male is reported. In general, male morphology has greater and more discrete variation than in females, but they are scarce in museum collections. Species distributions are updated and illustrated, the genus ranging from southern Colombia to northern Argentina, with no reliable records from the Guiana Shield and all nominal species occurring in Brazil. Intraspecific variation and natural history are discussed. New illustrated identification keys are provided for both sexes. Future studies should address the collection of fresh specimens for molecular work and to assess the conservation status of several species and populations.
Five new species of freshwater gastropods of the tateid genus Sulawesidrobia are described from the ancient Lake Matano on Sulawesi, Indonesia: S. wilsoni sp. nov., S. carsonae sp. nov., S. ehrlichi sp. nov., S. crutzeni sp. nov., and S. dinersteini sp. nov. The descriptions were based on shell morphology, anatomy as well as phylogenetic analysis using DNA sequence data of a fragment of the mitochondrial cytochrome oxidase I. All three suits of characters were included into the diagnoses. The new species formed a clade with two species from Lake Towuti, but separate from already known species from Lake Matano. The species were discovered between 2003 and 2005. However, not a single specimen of Sulawesidrobia was found when several sites were revisited in 2018 and 2019. This may be a consequence of the release of South American flowerhorn cichlid fish into the lake, in combination with heavy eutrophication of the once ultra-oligotrophic lake. It seems likely that several populations or even entire species of Sulawesidrobia in Lake Matano may be extinct. The species names given reflect this by acknowledging important conservationists.
A new species of the eutroglobiont gastropod taxon Zospeum Bourguignat, 1856 is described. Zospeum tholussum sp. n. is characterized based on a population from the Lukina Jama–Trojama cave system (Velebit Mts., Croatia). A single living specimen occurred at 980 m depth. The species is morphologically related to Zospeum amoenum (Frauenfeld, 1856), but can be readily distinguished from the latter by the presence of a weak columellar fold and its dome-like structured 2nd whorl. DNA barcoding is capable to clearly delineate Zospeum tholussum from other Zospeum spp. as well.
The genus Bennelongia De Deckker & McKenzie, 1981 is most likely endemic to Australia and New Zealand and, up to now, only two described species in this genus had been reported from Western Australia. Extensive sampling in Western Australia revealed a much higher specifi c diversity. Here, we describe nine new species in three lineages, within the genus Bennelongia: B. cygnus sp. nov. and B. frumenta sp. nov. in the B. cygnus lineage, B. gwelupensis sp. nov., B. coondinerensis sp. nov., B. cuensis sp. nov., B. lata sp. nov. and B. bidgelangensis sp. nov. in the B. australis lineage, and B. strellyensis sp. nov. and B. kimberleyensis sp. nov. (from the Pilbara and Kimberley regions respectively) in the B. pinpi-lineage. For six of the nine species, we were also able to construct molecular phylogenies and to test for cryptic diversity with two different methods based on the evolutionary genetic species concept, namely Birky’s 4 x rule and the GYMC model. These analyses support the specifi c nature of at least four of the fi ve new species in the B. australis lineage and of the two new species in the B. pinpi lineage. We also describe Bennelongiinae n.subfam. to accommodate the genus. With the nine new species described here, the genus Bennelongia now comprises 15 species, but several more await formal description.
The ostracod genus Bennelongia De Deckker & McKenzie, 1981 is endemic to Australia and New Zealand. Extensive sampling in Western Australia (WA) revealed a high specific and largely undescribed diversity. Here, we describe seven new species belonging to the B. barangaroo lineage: B. timmsi sp. nov., B. gnamma sp. nov., B. hirsuta sp. nov., B. ivanae sp. nov., B. mcraeae sp. nov., B. scanloni sp. nov. and B. calei sp. nov., and confirm the presence of an additional species, B. dedeckkeri, in WA. For five of these eight species, we could construct molecular phylogenies and parsimonious networks based on COI sequences. We also tested for cryptic diversity and specific status of clusters with a statistical method based on the evolutionary genetic species concept, namely Birky’s 4 theta rule. The analyses support the existence of these five species and a further three cryptic species in the WA B. barangaroo lineage. The molecular evidence was particularly relevant because most species described herein have very similar morphologies and can be distinguished from each other only by the shape, size and position of the antero-ventral lapel on the right valve, and, in sexual populations, by the small differences in shape of the hemipenes and the prehensile palps in males. Four species of the WA B. barangaroo lineage occur in small temporary rock pools (gnammas) on rocky outcrops. The other four species are mainly found in soft bottomed seasonal water bodies. One of the latter species, B. scanloni sp. nov., occurs in both claypans and deeper rock pools (pit gnammas). All species, except for B. dedeckkeri, originally described from Queensland, have quite clearly delimited distributions in WA. With the seven new species described here, the genus Bennelongia now comprises 25 nominal species but several more await formal description.