21,276 research outputs found

    Towards a revision of the South American genus Praocis Eschscholtz (Coleoptera, Tenebrionidae), with estimation of the diversity of each subgenus

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    A review of the subgenera of the South American genus Praocis Eschscholtz (Pimeliinae: Praociini) is presented. Praocis comprises 77 species and 8 subspecies arranged in nine subgenera distributed in arid lands from Central Peru and Bolivia to the Southern part of Patagonia in Chile and Argentina. For each subgenus of Praocis: Praocis Eschscholtz, Mesopraocis Flores & Pizarro-Araya, subgen. n., Anthrasomus Guérin-Méneville, Filotarsus Gay & Solier, Postpraocis Flores & Pizarro-Araya, subgen. n., Hemipraocis Flores & Pizarro-Araya, subgen. n., Orthogonoderes Gay & Solier, Praonoda Flores & Pizarro-Araya, subgen. n., and Praocida Flores & Pizarro-Araya, subgen. n., we present a diagnosis using new and constant characters of adult morphology such as clypeal configuration, length and proportion of antennomeres 9, 10 and 11, arrangement of apical tomentose sensory patches on antennomeres 10 and 11, anterior margin of prosternum, lateral margin of elytron, ventral surface of profemora, and shape of protibiae. An identification key for the nine subgenera of Praocis is presented. Type species are designated for the five new subgenera; for Mesopraocis: Praocis calderana Kulzer, for Postpraocis: Praocis pentachorda Burmeister, for Hemipraocis: Praocis sellata Berg, for Praonoda: Praocis bicarinata Burmeister, for Praocida: Praocis zischkai Kulzer, and for the previously described subgenus Orthogonoderes: Praocis subreticulata Gay & Solier. The current number of species and the estimated number of species to be described are presented. The distribution ranges of the subgenera, including new records from collections and recent expeditions, are given. Habitat preferences and a discussion of the biogeography of the genus are also presented.Fil: Flores, Gustavo Ernesto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto Argentino de Investigaciones de las Zonas Áridas. Provincia de Mendoza. Instituto Argentino de Investigaciones de las Zonas Áridas. Universidad Nacional de Cuyo. Instituto Argentino de Investigaciones de las Zonas Áridas; ArgentinaFil: Pizarro Araya, Jaime. Universidad de la Serena; Chil

    Faunal change in Cretaceous endemic shallow-marine bivalve genera/subgenera of the northeast Pacific

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    Endemic shallow-marine Cretaceous bivalves in the northeast Pacific region (NEP), extending from southwestern Alaska to the northern part of Baja California Sur, Mexico, are tabulated and discussed in detail for the first time. Twenty-three genera/subgenera are recognized. Their first appearance was in the Valanginian, and their biodiversity continued to be very low during the rest of the Early Cretaceous. The bivalves of the middle Albian Alisitos Formation in northern Baja California are excluded because they did not live in the NEP. The highest number (13) of NEP endemic bivalve genera/subgenera occurred during the Turonian, which was the warmest time of the Cretaceous. At the Turonian/Coniacian boundary, when cooler waters migrated southward, there was a moderate dropoff in endemics that persisted until an origination event near the beginning of the early Maastrichtian, when 11 were present. Five of the 11 were present also during the Turonian, but the others were newcomers. Only three survived the turnover associated with the “Middle Maastrichtian Event” (MME), and none survived the K/Pg boundary mass-extinction event

    The phylogeny of Anophelinae revisited: inferences about the origin and classification of Anopheles (Diptera: Culicidae)

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    © 2015 Royal Swedish Academy of Sciences. "This is the pre-peer reviewed version of the following article: Harbach, R. E. and I. J. Kitching (2016). "The phylogeny of Anophelinae revisited: inferences about the origin and classification of Anopheles (Diptera: Culicidae)." Zoologica Scripta 45(1): 34-47, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1111/zsc.12137/full. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.

    The phylogenetic conundrum of Lutzia(Diptera: Culicidae: Culicini): a cautionary account of conflict and support

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    This is an open access article, available to all readers online, published under a creative commons licensing (https://creativecommons.org/licenses/by/4.0/). This document is the author's submitted version of the journal article. You are advised to consult the publisher's version if you wish to cite from it

    Faunal diversity of Paederus Fabricius, 1775 (Coleoptera: Staphylinidae) in Iran

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    Beetles of the genus Paederus sensu stricto Fabricius, 1775 (Coleoptera: Staphylinidae) are often noticed because of their potency in inducing a dermal lesion, so-called linear dermatitis. This genus, which is placed in the tribe Paederini and subfamily Paederinae of Staphylinidae, currently comprises 490 species worldwide. Our study presents a short review of the former records of Paederus spp. in Iran plus some unpublished data. Field collections were done during March-October yearly (1997-2007) in northern and southern Iran and April-June from central, eastern, western and north-western Iran (2008-2009). The present study adds four species to the Iranian fauna of the genus Paederus, which are P. brevipennis Lacordaire, 1835, P. basalis Bernhauer, 1914, P. pubescens Cameron, 1914 and P. schoenherri Czwalina, 1899. Paederus brevipennis and P. schoenherri are the first members of the subgenus Harpopaederus Scheerpeltz, 1957, ever reported from Iran. Considering previous reports, museum-deposited materials and our findings, 14 species and subspecies of the genus Paederus, which are grouped in five subgenera, occur in Iran. These subgenera are Eopaederus Scheerpeltz, Harpopaederus Scheerpeltz, Heteropaederus Scheerpeltz, Paederus Fabricius and Poederomorphus des Cottes; however P. duplex spectabilis Bernhauer, 1913 is not yet attributed to any of the 13 so-far defined subgenera

    A taxonomic review of the subtribe Pericalina (Coleoptera: Carabidae: Lebiini) in the Western hemisphere : with descriptions of new species and notes about classification and zoogeography

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    A taxonomic review of the lebiine sub tribe Pericalina in the Western Hemisphere, this paper includes a treatment of the genus-groups, a key to the genera, keys to subgenera, species groups, and species of each polybasic genus, descriptions of new species and new subgenera, new locality records for previously described species, re-rankings, and new synonymy. In total, 111 species and subspecies are treated, 26 of which are described as new

    Phylogenetic relationships in Betula (Betulaceae) based on AFLP markers

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    The genus Betula comprises various species in boreal and temperate climate zones of the Northern Hemisphere. The taxonomy of Betula is controversial and complicated by parallel evolution of morphological traits, polyploidization events, and extensive hybridization and introgression among species. Multilocus molecular data from AFLPs were used to provide phylogenetic information. A large number of polymorphic markers (321 variable bands) were produced in 107 Betula accessions from 23 species and 11 hybrids. The AFLP results were largely congruent with the results from previously examined nuclear DNA markers. Four distinct subgenera were identified within the genus Betula. These subgenera were partly in disagreement with the traditional (but disputed) division of the genus. In addition, the results indicated several groups of conspecific taxa. The majority of the species fell within subgenus Betula and shared a high degree of similarity with B. pendula. All hybrids were associated with this group, and the AFLP data contained signals on putative parents for some of the interspecific hybrids. Subgenus Chamaebetula and part of the Neurobetula species should be merged with Betula. The subgenera Betulenta, Betulaster, and the remaining part of Neurobetula are distinct and well supported. Although our results indicate that four major taxonomic groups can be recognized within the genus Betula, the relationship between them remains unclear. This may be due to the occurrence of hybridization and introgression, which would have a homogenizing effect on the relationships between species. Naturally occurring Betula species of hybrid origin may explain the low bootstrap values within the Betula clade

    Three new species of Eupetersia Blüthgen, 1928 (Hymenoptera, Halictidae) from the Oriental Region

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    Three new species, Eupetersia (Nesoeupetersia) singaporensis sp. nov., collected in a mangrove swamp in Singapore, and Eupetersia (Nesoeupetersia) sabahensis sp. nov., collected in the mountains of Sabah, Borneo, and Eupetersia (Nesoeupetersia) yanegai sp. nov., collected in Thailand, are described. This genus is more diversified in the sub-Saharan region, including Madagascar. The only other Oriental species, E. nathani (Baker, 1974), was described from India and is diagnosed and re-illustrated here

    West Palaearctic species of the genus Diostracus Loew, 1861 (Diptera: Dolichopodidae)

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    A new status (as subgenera of Diostracus Loew, 1861) for Sphyrotarsus Mik, 1874, Lagodechia Negrobov & Tsurikov, 1996 and Ozmena Özdikmen, 2010 stat. nov. is proposed. A new species, Diostracus (Sphyrotarsus) kustovi sp. nov., is described from the Russian Caucasus. The following recombinations (comb. nov.) are also proposed: Diostracus (Sphyrotarsus) argyrostomus (Mik, 1874); D. (S.) caucasicus (Negrobov, 1965); D. (S.) hervebazini (Parent, 1914); D. (S.) hessei (Parent, 1914); D. (S.) hygrophilus (Becker, 1891); D. (S.) leucostomus (Loew, 1861); D. (S.) parenti (Hesse, 1933); D. (Lagodechia) spinulifer Negrobov & Tsurikov, 1988; and D. (Ozmena) stackelbergi (Negrobov, 1965). A key to ten Diostracus species inhabiting the West Palaearctic Region is provided

    Origins of neotropical leafy Hepaticae

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    The neotropical hepatic flora, predominantly constituted by members of the Jungermanniales and Metzgeriales, includes a disproportionate number of genera which are endemic (over 38) and a number which evidently originated here but have shown slight and in a geological sense, modern dispersal by solitary species. Endemism is confined almost to the Jungermanniales; it is to a large degree of a unique sort: confined to highly apomorphic derivatives, often extremely reduced, sometimes confervoid or thalloid (aside from 'normal' sexual branches). These endemics are derivatives of basically cool-Gondwanalandic suborders, chiefly Lepidoziineae and Cephaloziineae which, in the Antipodes today include a wide range of plesiomorphic taxa. The highest proportion of endemic genera, often stenotypic (1-3 species each) occurs in the upper montane zone: from upper Andean forest to páramo, to the edge of permanent snow and ice; a smaller number occurs at upper elevations of the Guyana Shield, but more occur in the riverine systems that dissect this shield. The taxa found there (i.a., Zoopsidella, Pteropsiella, Schusterolejeunea, Cephalantholejeunea) are among the most apomorphic of all hepatics. The amount of endemism is shown to be higher than in any comparable region of the globe. It is assumed that this is owing to: (a) isolation, exceeding 40 m.y. and probably exceeding 60 m.y.; (b) continuous tectonic activity, preserving the 'raw' and 'pioneer' habitats which are necessary for the survival of 'fugitive', 'shuttle' and other types of pioneer taxa; (c) the antiquity of the Guyana Shield and its riverine system; (d) creation of striking ecological gradients, many biotic islands; (e) fluctuation in extent and degree of isolation of these 'islands', leading to (f) rapid evolution due to genetic drift and perhaps enhanced selection pressures. It is concluded that part of the complexity of the flora is due to preservation of some elements on the old Guyana Shield but most is due to relatively rapid evolution during Tertiary times. A final contributing element has been the fact that movement of the South American plate has been primarily from east to west, so that the relevant land area has not been rafted into regions with very different climatic parameters: the degree of extinction seen in, e.g., India and Australia is not evident here. It is concluded that the amount of endemism seen, and its extreme kinds, 'need' in excess of the 40-60 m.y. time span which seems available. In particular, the large number of high elevation endemics, some (such as Ruizanthus) very isolated, cannot be satisfactorily explained by assuming their evolution in the few million years available since alpine regions were created by the rise of the Andes. It is almost necessary to conclude that limited 'pre-Andes' must have existed and that the ancestors of the isolated taxa seen today in alpine loci in Colombia and Venezuela originated elsewhere. The other side of the outlined scenario is that with the near-total isolation of tropical America until the Andes were elevated, and until the Pliocene connection to North America arose, one would expect to see few and scattered intruders from cool-Gondwanalandic areas and from Laurasia. The modern flora reflects exactly this
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