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An annotated world catalogue and bibliography of the cucujoid family Propalticidae (Coleoptera) is presented. Each taxon is accompanied by a complete taxonomic history, including a full annotated synonymy with original references cited, and current location and status of primary types. The name Slipinskogenia nom. nov. is proposed to replace Discogenia Kolbe, 1897, junior homonym of Discogenia LeConte, 1866, resulting in 11 new combinations. A key is provided for separation of the two genera included in the family. Complete published and previously unpublished distributional data are given.
Eight species of the genus Psilotreta Banks (Trichoptera: Odontoceridae) are currently known from Vietnam: P. albogera Mey 1997, P. androconiata Mey 1997, P. bidens Mey 1995, P. enikoae Oláh and Johanson 2010, P. frigidaria Mey 1996, P. jaroschi Malicky 1995, P. papaceki Malicky 1995, P. spitzeri Malicky 1995. A new species, Psilotreta kurenschikovorum, from Thua Thien-Hue Province is herein described. The new species differs from other species of the genus by peculiarities in wing venation, by the unusual shape of epicranial suture on the head, and by the bifid apical segment of the inferior appendage. Additional province and collection information for previously recorded species are included.
This paper summarizes the published information on the beetle fauna of the northern Leeward Islands (Anguilla, Antigua, Barbuda, Nevis, Saba, St. Barthélemy, St. Eustatius, St. Kitts, St. Martin-St. Maarten, and smaller associated islands, excluding Montserrat). These islands are generally smaller, lower, and drier than the remaining Leeward and Windward islands of the Lesser Antilles island arc. The fauna contains 26 families, with 155 genera, and 218 species. The families with the largest number of recorded species are Staphylinidae (36), Cerambycidae (28), Scarabaeidae (25), Tenebrionidae (23), Curculionidae (18), and Carabidae (15). At least 7 species (3.2% of the fauna) were probably introduced to the island by human activities. Sixteen species (7.3%) are endemic (restricted) to a single paleo-island bank and likely speciated there. Twenty nine species (13.3%) are shared only with other islands of the Lesser Antilles (Lesser Antillean endemics), and 43 species (19.7%) are more widespread Antilles endemics. The remaining 123 species (56.4%) in the fauna are otherwise mostly widely distributed in the Antilles and the Neotropical Region. The local beetle fauna is largely an immigrant fauna and has mostly originated elsewhere than on the islands of the northern Leewards. Summary data on total species endemicity of the entire Lesser Antilles indicate the presence of at least 1278 endemic beetle species, which is a density of about 20.7 species per 100 km2. This is now equivalent to that of the endemic vascular plants of the Caribbean islands. This truly makes the Caribbean islands a biodiversity hotspot for beetles. For the northern Leewards, it is evident that the beetle diversity is markedly understudied, and that the actual number of species is many times higher than now known.
Curculionoidea (Coleoptera) of the West Indian island of Dominica are composed of 111 genera and 214 species and subspecies. Some of the species listed are morphospecies, or are known to be undescribed, but all are identified at least to genus. Previously the fauna was recorded as 31 species. Numbers presented herein represent a seven-fold increase in species diversity. Furthermore, the widespread nature of many species demonstrates that the supposedly endemic faunas of many West Indian islands may be based on collecting biases or a lack of people capable of providing species level identifications.
The biogeographic significance of Diplopoda is substantiated by 50 maps documenting indigenous occurrences of the 16 orders, the three Spirostreptida s. l. suborders – Cambalidea, Epinannolenidea, Spirostreptidea – and all higher taxa including Diplopoda itself. The class is indigenous to all continents except Antarctica and islands/archipelagos in all temperate and tropical seas and oceans except the Arctic; it ranges from Kodiak Island and the northern Alaskan Panhandle, United States (USA), southern Hudson Bay, Canada, and near or north of the Arctic Circle in Iceland, continental Scandinavia, and Siberia to southern “mainland” Argentina, the southern tips of Africa and Tasmania, and Campbell Island, subantarctic New Zealand. The vast, global distribution is interrupted by sizeable, poorly- or unsampled areas including the Great Basin, USA; the Atacama Desert region of Chile and neighboring countries; southern South American islands; the central Kalahari and Sahara deserts; the Gobi Desert, Mongolia, and all of north-central and western China; from north of the Caspian Sea, Russia, to central Kazakhstan; and the “Outback” of central Australia. Five Arabian countries lack both samples and published records of indigenous diplopods – Bahrain, Kuwait, Oman, Qatar, and United Arab Emirates – as do Turks and Caicos, in the New World, and Mauritania and possibly Egypt, Africa. New records, including the first for Chilognatha from Botswana and the first specific localities from Northern Territory, Australia, are cited in the Appendix. Increased emphasis on mappings in taxonomic research is warranted along with investigations of insular “species swarms” that constitute a microcosm of the early evolution of the class. The largest “species swarm” in the Diplopoda is Diplopoda itself!
Pocket gopher burrows (Rodentia: Geomyidae) were sampled from five previously unsampled localities in northern Louisiana to determine the associated faunal composition of Histeridae and Scarabaeidae (Coleoptera). Sampling produced four species of Histeridae and seven species of Scarabaeidae, all of which had been previously reported from Louisiana. The most commonly collected scarab beetle was Cryptoscatomaseter haldemani (Horn) followed by Geomyphilus insolitus (Brown). Onthophilus kirni Ross was the most commonly collected hister beetle.
Background: The interferon-inducible immunity-related GTPases (IRG proteins/p47 GTPases) are a distinctive family of GTPases that function as powerful cell-autonomous resistance factors. The IRG protein, Irga6 (IIGP1), participates in the disruption of the vacuolar membrane surrounding the intracellular parasite, Toxoplasma gondii, through which it communicates with its cellular hosts. Some aspects of the protein's behaviour have suggested a dynamin-like molecular mode of action, in that the energy released by GTP hydrolysis is transduced into mechanical work that results in deformation and ultimately rupture of the vacuolar membrane. Results: Irga6 forms GTP-dependent oligomers in vitro and thereby activates hydrolysis of the GTP substrate. In this study we define the catalytic G-domain interface by mutagenesis and present a structural model, of how GTP hydrolysis is activated in Irga6 complexes, based on the substrate-twinning reaction mechanism of the signal recognition particle (SRP) and its receptor (SRalpha). In conformity with this model, we show that the bound nucleotide is part of the catalytic interface and that the 3'hydroxyl of the GTP ribose bound to each subunit is essential for trans-activation of hydrolysis of the GTP bound to the other subunit. We show that both positive and negative regulatory interactions between IRG proteins occur via the catalytic interface. Furthermore, mutations that disrupt the catalytic interface also prevent Irga6 from accumulating on the parasitophorous vacuole membrane of T. gondii, showing that GTP-dependent Irga6 activation is an essential component of the resistance mechanism. Conclusions: The catalytic interface of Irga6 defined in the present experiments can probably be used as a paradigm for the nucleotide-dependent interactions of all members of the large family of IRG GTPases, both activating and regulatory. Understanding the activation mechanism of Irga6 will help to explain the mechanism by which IRG proteins exercise their resistance function. We find no support from sequence or G-domain structure for the idea that IRG proteins and the SRP GTPases have a common phylogenetic origin. It therefore seems probable, if surprising, that the substrate-assisted catalytic mechanism has been independently evolved in the two protein families.