Refine
Year of publication
Document Type
- Part of Periodical (13)
- Article (3)
Language
- English (16)
Has Fulltext
- yes (16)
Is part of the Bibliography
- no (16)
Keywords
- taxonomy (8)
- biodiversity (6)
- Ostracoda (4)
- Western Australia (4)
- cryptic species (3)
- evolution (3)
- Cyprididae (2)
- Evolution (2)
- Taxonomy (2)
- distribution (2)
Institute
- Medizin (1)
Necroptosis contributes to the pathophysiology of several inflammatory, infectious and degenerative disorders. TNF-induced necroptosis involves activation of the receptor-interacting protein kinases 1 and 3 (RIPK1/3) in a necrosome complex, eventually leading to the phosphorylation and relocation of mixed lineage kinase domain like protein (MLKL). Using a high-content screening of small compounds and FDA-approved drug libraries, we identified the anti-cancer drug Sorafenib tosylate as a potent inhibitor of TNF-dependent necroptosis. Interestingly, Sorafenib has a dual activity spectrum depending on its concentration. In murine and human cell lines it induces cell death, while at lower concentrations it inhibits necroptosis, without affecting NF-κB activation. Pull down experiments with biotinylated Sorafenib show that it binds independently RIPK1, RIPK3 and MLKL. Moreover, it inhibits RIPK1 and RIPK3 kinase activity. In vivo Sorafenib protects against TNF-induced systemic inflammatory response syndrome (SIRS) and renal ischemia–reperfusion injury (IRI). Altogether, we show that Sorafenib can, next to the reported Braf/Mek/Erk and VEGFR pathways, also target the necroptotic pathway and that it can protect in an acute inflammatory RIPK1/3-mediated pathology.
We describe one new tribe, two new genera and three new species of the subfamily Cypridopsinae Kaufmann, 1900 from Brazilian floodplains. Brasilodopsis gen. nov. belongs in the nominal tribe Cypridopsini, and both new species in this new genus were found in both sexual and asexual populations. Brasilodopsis baiabonita gen. et sp. nov. has a wide distribution and was found in three of the four major Brazilian floodplains. Brasilodopsis amazonica gen. et sp. nov. was recorded only from the Amazon floodplain. Brasilodopsis baiabonita gen. et sp. nov. has a subtriangular shape in lateral view, whereas Brasilodopsis amazonica gen. et sp. nov. is more elongated and has more rounded dorsal margins in both valves, as well as more pronounced external valve ornamentation, consisting of rimmed pores in shallow pits. Paranadopsis reducta gen. et sp. nov. was found in asexual populations in the Upper Paraná River floodplain only and differs from other Cypridopsinae in the more elongated carapace, an A1 with strongly reduced chaetotaxy (hence the specific name) and the total absence of caudal rami in females. Because of these strong reductions in valve and limb morphology, Paranadopsini trib. nov. is created within the Cypridopsinae for this intriguing new genus and species.
The ostracod genus Bennelongia De Deckker & McKenzie, 1981 occurs in Australia and New Zealand. We redescribe B. nimala from the Northern Territory and describe six new species from Western Australia belonging to the B. nimala (five species) and B. triangulata sp. nov. (one species) lineages: B. tirigie sp. nov., B. koendersae sp. nov., B. pinderi sp. nov., B. muggon sp. nov., B. shieli sp. nov. and B. triangulata sp. nov. For six of these seven species, we could construct molecular phylogenies and parsimonious networks based on COI sequences. We tested for specific status and for potential cryptic diversity of clades with Birky’s 4 theta rule. The analyses support the existence of these six species and the absence of cryptic species in these lineages. Bennelongia triangulata sp. nov. is a common species in the turbid claypans of the Murchison/Gascoyne region. Bennelongia nimala itself is thus far known only from the Northern Territory. Bennelongia tirigie sp. nov., B. pinderi sp. nov. and B. muggon sp. nov. occur in the Murchison/Gascoyne region, whereas B. koendersae sp. nov. and B. shieli sp. nov. are described from the Pilbara. With the six new species described here, the genus Bennelongia now comprises 31 nominal species.
The New Caledonian Archipelago is a hot spot for biodiversity and endemism. Whereas popular groups such as birds and plants are well-studied, invertebrate groups such as ostracods remain ill-known. Here, we re-describe Strandesia sanoamuangae Savatenalinton & Martens, 2010, originally described from Thailand (8000 km away from New Caledonia), and describe Strandesia mehesi sp. nov. Both species are known only from females. Material for the present study was collected from diverse aquatic non-marine habitats from Grande Terre, the main island of New Caledonia. Whereas S. sanoamuangae is seemingly easily identifiable, S. mehesi sp. nov. is part of the Strandesia vinceguerrae/vavrai species cluster in the genus, of which the 'older' species (described long ago) often have incomplete and superficial descriptions. Differentiation between the new species and the other members of this species cluster are based on small anatomical details of the valves. The current paper updates the known number of recent freshwater Ostracoda of New Caledonia from 14 to 16 species, although at least five of these species have an uncertain status.
This paper describes a set of guidelines for the citation of zoological and botanical specimens in the European Journal of Taxonomy. The guidelines stipulate controlled vocabularies and precise formats for presenting the specimens examined within a taxonomic publication, which allow for the rich data associated with the primary research material to be harvested, distributed and interlinked online via international biodiversity data aggregators. Herein we explain how the EJT editorial standard was defined and how this initiative fits into the journal's project to semantically enhance its publications using the Plazi TaxPub DTD extension. By establishing a standardised format for the citation of taxonomic specimens, the journal intends to widen the distribution of and improve accessibility to the data it publishes. Authors who conform to these guidelines will benefit from higher visibility and new ways of visualising their work. In a wider context, we hope that other taxonomy journals will adopt this approach to their publications, adapting their working methods to enable domain-specific text mining to take place. If specimen data can be efficiently cited, harvested and linked to wider resources, we propose that there is also the potential to develop alternative metrics for assessing impact and productivity within the natural sciences.
Five new species in four new genera from Western Australia are described. All species have valve characters that are reminiscent of the genus Heterocypris Claus, 1892 and also have similar valve outlines, with highly arched valves. However, all species have a hemipenis morphology that is totally different from the typical form in Heterocypris. In Patcypris gen. nov. (with type species P. outback gen. et sp. nov.), the lateral lobe is large and shaped as a pickaxe, while the medial lobe is divided into two distal lobes. Trilocypris gen. nov. (with type species T. horwitzi gen. et sp. nov.) is characterised by a hemipenis that has three, instead of two, distal lobes. In Bilocypris gen. nov. (with type species B. fortescuensis gen. et sp. nov. and a second species, B. mandoraensis gen. et sp. nov.), the lateral lobe of the hemipenis is spatulate, rather than boot-shaped, and the medial lobe is bilobed. Billcypris gen. nov. (with type species B. davisae gen. et sp. nov.) has a large and sub-rectangular lateral lobe and a pointed medial lobe. We discuss the taxonomic value of the traditional and new morphological characters and speculate that the diversity of this cluster of genera and species may be greater than currently known.
The New Caledonia archipelago is known for its high level of endemism in both faunal and floral groups. Thus far, only 12 species of non-marine ostracods have been reported. After three expeditions to the main island of the archipelago (Grande Terre), about four times as many species were found, about half of which are probably new. Here, we describe a new species, Cyprinotus drubea sp. nov., which is characterised mainly by the hyper-developed dorsal hump on the right valve, much larger than in any other known Recent species in this genus. After a literature study of the other presumed species in Cyprinotus Brady, 1886, we retain seven Recent species in the genus, including the present new species. Cyprinotus crenatus (Turner, 1893), C. dentatus (Sharpe, 1910), C. flavescens Brady, 1898, C. inconstans Furtos, 1936, C. newmexicoensis Ferguson, 1967, C. ohanopecoshensis Ferguson, 1966, C. pellucidus (Sharpe, 1897), C. scytodus (Dobbin, 1941) and C. sulphurous Blake, 1931 are here all referred to the genus Heterocypris s. lat. Claus, 1892. Cyprinotus unispinifera Furtos, 1936 is assigned to the genus Cypricercus Sars, 1895. Cyprinotus tenuis Henry, 1923, C. fuscus Henry, 1919 and C. carinatus (King, 1855) are here classified as doubtful species. A checklist of the 14 non-marine ostracods, now including Cyprinotus drubea sp. nov. and Cypris granulata (Daday, 1910), thus far reported from New Caledonia, is provided. Herpetocypris caledonica Méhes, 1939 and H. caledonica var. minor Méhes, 1939 are synonymised with Candonocypris novaezelandiae (Baird, 1843).
We present an updated, subjective list of the extant, non-marine ostracod genera and species of the world, with their distributions in the major zoogeographical regions, as well as a list of the genera in their present hierarchical taxonomic positions. The list includes all taxa described and taxonomic alterations made up to 1 July 2018. Taxonomic changes include 17 new combinations, 5 new names, 1 emended specific name and 11 new synonymies (1 tribe, 4 genera, 6 species). Taking into account the recognized synonymies, there are presently 2330 subjective species of non-marine ostracods in 270 genera. The most diverse family in non-marine habitats is the Cyprididae, comprising 43.2% of all species, followed by the Candonidae (29.0%), Entocytheridae (9.1%) and the Limnocytheridae (7.0%). An additional 13 families comprise the remaining 11.8% of described species. The Palaearctic zoogeographical region has the greatest number of described species (799), followed by the Afrotropical region with 453 species and the Nearctic region with 439 species. The Australasian and Neotropical regions each have 328 and 333 recorded species, respectively, while the Oriental region has 271. The vast majority of non-marine ostracods (89.8%) are endemic to one zoogeographical region, while only six species are found in six or more regions. We also present an additional list with 'uncertain species', which have neither been redescribed nor re-assessed since 1912, and which are excluded from the main list; a list of taxonomic changes presented in the present paper; a table with the number of species and % per family; and a table with numbers of new species described in the 20-year period between 1998 and 2017 per zoogeographical region. Two figures visualize the total number of species and endemic species per zoogeographical region, and the numbers of new species descriptions per decade for all families and the three largest families since 1770, respectively.
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.
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.