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1.
Crews SC  Harvey MS 《ZooKeys》2011,(99):1-104
We relimit and revise the family Selenopidae to include four new genera and 27 new species from Australia and the Oriental Region. The family is redefined, as are the genera Anyphops Benoit, Garcorops Corronca, Hovops Benoit, Selenops Latreille, and Siamspinops Dankittipakul & Corronca, to accommodate the new genera and to correct previous inconsistencies in the diagnoses and definitions of the aforementioned genera. The species of Selenops that occur throughout India and China are also reviewed. Three species occur in China: Selenops bursarius Karsch 1879, also known from Japan, Korea and Taiwan, Selenops ollarius Zhu, Sha, & Chen 1990, and Selenops radiatus Latreille 1819, the type of the genus and most widespread selenopid. Selenops cordatus Zhu, Sha & Chen syn. n. is recognized as a junior synonym of Selenops radiatus. Amamanganopsgen. n. is monotypic, with Amamanganops baginawasp. n. (♀; from the Philippines). Godumopsgen. n. is monotypic, with Godumops caritussp. n. (♂; from Papua New Guinea). Karaopsgen. n. occurs throughout Australia and includes 24 species. A new combination is proposed for Karaops australiensis (L. Koch 1875) comb. n. (ex. Selenops), and the new species: Karaops gangariesp. n. (♀, ♂), Karaops monteithisp. n. (♀), Karaops alanlongbottomisp. n. (♂), Karaops keithlongbottomisp. n. (♂), Karaops larryoosp. n. (♂), Karaops jarritsp. n. (♂,♀), Karaops marrayagongsp. n. (♀), Karaops ravenisp. n. (♂,♀), Karaops badgeraddasp. n. (♀), Karaops burbidgeisp. n. (♂,♀), Karaops karrawarlasp. n. (♂,♀), Karaops julianneaesp. n. (♀), Karaops martamartasp. n. (♀), Karaops manaaynsp. n. (♀, ♂), Karaops vadlaadambarasp. n. (♀, ♂), Karaops pilkingtonisp. n. (♀, ♂), Karaops deserticolasp. n. (♀), Karaops ngarutjaranyasp. n. (♂,♀), Karaops francesaesp. n. (♂,♀), Karaops toolbrunupsp. n. (♀, ♂), the type species Karaops ellenaesp. n. (♂,♀), Karaops jenniferaesp. n. (♀), and Karaops dawarasp. n. (♀).The genus Makdiopsgen. n. contains five species from India and Nepal. A new combination is proposed for Makdiops agumbensis (Tikader 1969), comb. n., Makdiops montigenus (Simon 1889), comb. n., Makdiops nilgirensis (Reimoser 1934) comb. n.,(ex. Selenops). Also, there are two new species the type of the genus Makdiops mahishasurasp. n. (♀; from India), and Makdiops shivasp. n. (♀). The genus Pakawopsgen. n. is monotypic. A new combination is proposed for Pakawops formosanus (Kayashima 1943) comb. n. (ex. Selenops), known only from Taiwan. A new combination is proposed for Siamspinops aculeatus (Simon)comb. n. (ex. Selenops). The distribution and diversity of the studied selenopid fauna is discussed. Finally, keys are provided to all of the selenopid genera and to the species of Karaopsgen. n.and Makdiopsgen. n.  相似文献   

2.
The large genus Orthomorpha is rediagnosed and is shown to currently comprise 51 identifiable species ranging from northern Myanmar and Thailand in the Northwest to Lombok Island, Indonesia in the Southeast. Of them, 20 species have been revised and/or abundantly illustrated, based on a restudy of mostly type material; further 12 species are described as new: Orthomorpha atypicasp. n., Orthomorpha communissp. n., Orthomorpha isarankuraisp. n., Orthomorpha picturatasp. n., Orthomorpha similanensissp. n., Orthomorpha suberectasp. n., Orthomorpha tuberculiferasp. n.,Orthomorpha subtuberculiferasp. n. and Orthomorpha latitergasp. n., all from Thailand, as well as Orthomorpha elevatasp. n.,Orthomorpha spiniformissp. n. and Orthomorpha subelevatasp. n., from northern Malaysia. The type-species Orthomorpha beaumontii (Le Guillou, 1841) is redescribed in due detail from male material as well, actually being a senior subjective synonym of Orthomorpha spinala (Attems, 1932), syn. n. Two additional new synonymies are proposed: Orthomorpha rotundicollis (Attems, 1937) = Orthomorpha tuberculata (Attems, 1937), syn. n., and Orthomorpha butteli Carl, 1922 = Orthomorpha consocius Chamberlin, 1945, syn. n., the valid names to the left. All species have been keyed and all new and some especially widespread species have been mapped. Further six species, including two revised from type material, are still to be considered dubious, mostly because their paraterga appear to be too narrow to represent Orthomorpha species. A new genus, Orthomorphoidesgen. n., diagnosed versus Orthomorpha through only moderately well developed paraterga, coupled with a poorly bi- or trifid gonopod tip, with at least some of its apical prongs being short spines, is erected for two species: Orthomorpha setosus (Attems, 1937), the type-species, which is also revised from type material, and Orthomorpha exaratus (Attems, 1953), both comb. n. ex Orthomorpha.  相似文献   

3.
Morffe J  García N 《ZooKeys》2011,(78):1-14
Longior zayasi Coy, García & Alvarez, 1993 is established as incertae sedis because the males (declared as the holotype) are inconsistent with the generic diagnosis, particularly in relation to the morphology of the head and tail. Thus, the females of Longior zayasi species (which agree with the generic diagnosis) are renamed and re-described as Longior longior Morffe & García sp. n. We also described males found in the sample and considered as conspecific with the new species. A comparative table with the measurements of the most of the records of Longior longior is given. The male of Longior similis Morffe, García & Ventosa, 2009 is described from the type locality of the species and compared with the known males of the genus. A key to the females of the Cuban Longior is given.  相似文献   

4.
Bashkuev AS 《ZooKeys》2011,(130):263-279
The family Mesopanorpodidae is revised. Most taxa referred to this family are not related to the type genus Mesopanorpodes Tillyard, 1918. The type species of the latter, Mesopanorpodes wianamattensis,is closely related to Mesopsyche Tillyard, 1917. Therefore Mesopanorpodes is transferred to Mesopsychidae Tillyard, 1917 (= Mesopanorpodidae Tillyard, 1918, syn. n.).The earliest Mesopsychidae are described from the Upper Permian of European Russia (Severodvinian; Isady locality, Vologda Province): Permopsyche issadensisgen. etsp. n. (type species) and Permopsyche rasnitsynisp. n. Two species described under Mesopanorpodes from the Upper Permian of Australia are also included into Permopsyche: Permopsyche belmontensis (Riek, 1953), comb. n., Permopsyche robustus (Riek, 1953) comb. n. The first pre-Triassic Mesopsyche, Mesopsyche incompletasp. n. is described from the uppermost Permian (the town of Vyazniki, Vladimir Province). Bittacopanorpa javorskii Zalessky, 1935 from the uppermost Permian or basal Triassic of Kuznetsk Basin is identified as a hindwing of Mesopsyche: Mesopsyche javorskii (Zalessky, 1935) comb. n. The origin, evolutionary history, and stratigraphic occurrence of Mesopsychidae are discussed.  相似文献   

5.
Li CL  Wang CC  Keith D  Yang PS 《ZooKeys》2012,(177):37-48
Two new species of the Oriental scarab genus Tocama Reitter, 1902, Tocama laosensissp. n. and Tocama procerasp. n., are described from Indochina with diagnoses, distributions, remarks and illustrations. A key to the species of the genus is provided with a checklist with several nomenclatural changes: Hoplosternus tonkinensis Moser, 1913 is transferred to Tocama; Hoplosternus pygidialis Moser, 1915 syn. n., Tocama atra atra Keith, 2006 syn. n. and Tocama atra reichenbachi Keith, 2007 syn. n. = Tocama tonkinensis (Moser).  相似文献   

6.
All species of the genus Alphitobius Stephens, 1829 (Alphitobiini Reitter, 1917, subfamily Tenebrioninae Latreille, 1802) from Africa and adjacent islands are revised. New species: Alphitobius capitaneus sp. n. from Kenya. New synonyms: Cryptops ulomoides Solier, 1851, syn. n. of Alphitobius diaperinus (Panzer, 1796); Alphitobius rufus Ardoin, 1976, syn. n. of Alphitobius hobohmi Koch, 1953); Peltoides (Micropeltoides) crypticoides Pic, 1916, syn. n. of Peltoides (Micropeltoides) opacus (Gerstaecker, 1871), comb. n. Homonym: Alphitobius ulomoides Koch, 1953 = Alphitobius arnoldi nom. n. New combinations from Alphitobius: Ulomoides basilewskyi (Ardoin, 1969), comb. n.; Peltoides (Micropeltoides) opacus (Gerstaecker, 1871), comb. n. Figures of all examined species are added and a species key is compiled.  相似文献   

7.
The Australian Thrasorinae are revised and Mikeius is transferred to Mikeiinae Paretas-Martínez & Pujade-Villar, subfam. n., and Mikeius clavatus Pujade-Villar & Restrepo-Ortiz, sp. n., is described. Two new genera of Thrasorinae are erected: Cicatrix Paretas-Martínez, gen. n., including Cicatrix pilosiscutum(Girault), comb. n. from Amblynotus, Cicatrix schauffi (Buffington), comb. n. from Mikeius, and Cicatrix neumannoides Paretas-Martínez & Restrepo-Ortiz, sp. n.; and Palmiriella Pujade-Villar & Paretas-Martínez, gen. n., including Palmiriella neumanni (Buffington), comb. n. from Mikeius, Thrasorus rieki Paretas-Martínez & Pujade-Villar, sp. n., is also described. A phylogenetic analysis of 176 morphological and biological characters, including all these new taxa and all genera previously included in Thrasorinae, was conducted. All subfamilies were recovered as monophyletic, with the following relationships: Parnipinae (Euceroptrinae (Mikeiinae (Plectocynipinae (Thrasorinae)))). A worldwide key to the subfamilies of Figitidae is provided that includes the new subfamily, as well as a key to genera Thrasorinae.  相似文献   

8.
The praying mantis genus Liturgusa Saussure, 1869 occurs only in Central and South America and represents the most diverse genus of Neotropical Liturgusini (Ehrmann 2002). The genus includes bark dwelling species, which live entirely on the trunks and branches of trees and run extremely fast. All species included within the genus Liturgusa are comprehensively revised with a distribution stretching from central Mexico, the island of Dominica to the southeastern regions of Brazil and southern Bolivia. All known species are redescribed to meet the standards of the new treatment of the genus (11 species). Three new genera are described including Fuga gen. n., Velox gen. n., and Corticomantis gen. n. for species previously included in Liturgusa as well as Hagiomantis. Liturgusa mesopoda Westwood, 1889 is moved to within the previously described genus Hagiomantis Audinet Serville, 1838. A total of 19 species are newly described within Liturgusa, Fuga, and Velox including L. algorei sp. n., L. bororum sp. n., L. cameroni sp. n., L. cura sp. n., L. dominica sp. n., L. fossetti sp. n., L. kirtlandi sp. n., L. krattorum sp. n., L. manausensis sp. n., L. maroni sp. n., L. milleri sp. n., L. neblina sp. n., L. purus sp. n., L. stiewei sp. n., L. tessae sp. n., L. trinidadensis sp. n., L. zoae sp. n., F. grimaldii sp. n., and V. wielandi sp. n. Four species names are synonymized: Liturgusa peruviana Giglio-Tos, 1914, syn. n. = Liturgusa nubeculosa Gerstaecker, 1889 and Hagiomantis parva Piza, 1966, syn. n., Liturgusa sinvalnetoi Piza, 1982, syn. n., and Liturgusa parva Giglio-Tos, 1914, syn. n. = Mantis annulipes Audinet Serville, 1838. Lectotypes are designated for the following two species: Liturgusa maya Saussure & Zehntner, 1894 and Fuga annulipes (Audinet Serville, 1838). A male neotype is designated for Liturgusa guyanensis La Greca, 1939. Males for eight species are described for the first time including Liturgusa cayennensis Saussure, 1869, Liturgusa lichenalis Gerstaecker, 1889, Liturgusa guyanensis La Greca, 1939, Liturgusa maya Saussure & Zehntner, 1894, Liturgusa nubeculosa Gerstaecker, 1889, Fuga annulipes (Audinet Serville, 1838), Corticomantis atricoxata (Beier, 1931), and Hagiomantis mesopoda (Westwood, 1889). The female of Fuga fluminensis (Piza, 1965) is described for the first time. Complete bibliographic histories are provided for previously described species. The spelling confusion surrounding Liturgusa/Liturgousa is resolved. Full habitus images for males and females are provided for nearly all species. Habitus and label images of type specimens are provided when possible. Diagnostic illustrations of the head and pronotum for males and females are provided for all species when possible. Illustrations of male genital structures are provided for all species for which males are known. Measurement data, including ranges and averages, are provided for males and females of all species. Combined male and female genus and species level dichotomous keys are provided with a Spanish translation. A complete table of all examined specimens lists label data, museum codes, repositories, and other specimen specific information. A KML file with all georeferenced locality records is downloadable from mantodearesearch.com for viewing in Google Earth. Natural history information is provided for species observed by the author.  相似文献   

9.
10.
A molecular phylogeny of the species from the Trechus brucki clade (previously Trechus uhagoni group)based on fragments of four mitochondrial genes and one nuclear gene is given. We describe Trechus (Trechus) bouillonisp. n. from the western pre-Pyrenees: Sierras de Urbasa-Andía, Navarra, Spain. The species was collected in mesovoid shallow substratum (mss), a subterranean environment. Molecular as well as morphological evidences demonstrate that the new species belongs to the Trechus brucki clade. A narrow endemic species of high altitude in western French Pyrenees merged with Trechus brucki Fairmaire, 1862a, Trechus bruckoidessp. n., is described. A lectotype is designated for Trechus brucki and Trechus planiusculus Fairmaire, 1862b (junior synonym of Trechus brucki). The species group is redefined based on molecular and morphological characters, and renamed as the brucki group, as Trechus brucki was the first described species of the clade. A unique synapomorphy of the male genitalia, a characteristic secondary sclerotization of the sperm duct, which is shared by all the species of the brucki group sensu novo, is described and illustrated. The Trechus brucki group sensu novo is composed of Trechus beusti (Schaufuss, 1863), Trechus bouillonisp. n., Trechus brucki, Trechus bruckoidessp. n., Trechus grenieri Pandellé, 1867, T. uhagoni uhagoni Crotch, 1869, T. uhagoni ruteri Colas, 1935 and Trechus pieltaini Jeannel, 1920. We discuss the taxonomy of the group and provide illustrations of structures showing the differences between the species, along with distribution data and biogeographical comments.  相似文献   

11.
Twenty five South American species of the genus Selenops (Araneae, Selenopidae) are revised, of which three new taxa are described and illustrated: S. angelae and S. marilus (?, from Ecuador and Venezuela, respectively) and S. tiky (?, from Venezuela). Selenops ecuadorensis Berland, S. galapagoensis Banks, S. isopodus Mello-Leitão and S. melanurus Mello-Leitão are redescribed. Diagnostic characters of previously known species are given and the male palp and female genitalia are described and illustrated, some for the first time. New data on geographic distribution extend the ranges of some previously known species. A key to South American species is provided for the first time. En este trabajo se revisa el género Selenops (Araneae, Selenopidae) para América del Sur. Este género está representado por 25 especies, de las cuales aqu¡ se describen e ilustran tres especies nuevas, S. angelae y S. marilus (conocidas sólo por el macho de Ecuador y Venezuela, respectivamente) y S. tiky (sólo por la hembra de Venezuela). Se redescriben Selenops ecuadorensis Berland, S. galapagoensi s Banks, S. isopodus Mello-Leitão y S. melanurus Mello-Leitão y se ilustran, en algunos casos por primera vez, la genitalia de la hembra y el palpo del macho de todas las especies sudamericanas de Selenops. Se da la diagnosis de cada especie, se presentan mapas ampliando el área de distribución de la mayoría de las especies conocidas y se proporciona la primera clave para las especies sudamericanas.  相似文献   

12.
S Zonstein  YM Marusik 《ZooKeys》2012,(211):71-99
The Chinese representatives of Raveniola Zonstein, 1987 are currently recognized to comprise seven species. Four new species - Raveniola montanasp. n. (♂♀), Raveniola shangrilasp. n. (♂), Raveniola songisp. n. (♂) and Raveniola yunnanensissp. n. (♂) - are described from the highlands of Yunnan Province, China. According to some characters (shape of the palpus, palpal tibia and tibia I in males) they can be placed together with Raveniola hebeinica Zhu, Zhang & Zhang, 1999 and with Raveniola guangxi (Raven & Schwendinger, 1995), comb. n., transferred here from Sinopesa Raven & Schwendinger, 1995. The current generic position of Raveniola xizangensis (Hu & Li, 1987) is confirmed. Other Chinese nemesiids referred previously to Raveniola are transferred to Sinopesa: Sinopesa chinensis (Kulczyński, 1901), comb. n., Sinopesa sinensis (Zhu & Mao, 1983), comb. n. and Sinopesa chengbuensis (Xu & Yun, 2002), comb. n. The relationships between these Asian genera and their relations to Afrotropical nemesiids are discussed.  相似文献   

13.
This systematic study recognizes and describes 14 species of the genus Mallos O. Pickard-Cambridge, 1902 and three species of the genus Mexitlia Lehtinen, 1967. Three species of Mallos – Mallos gertschi, Mallos chamberlini and Mallos macrolirus –and one species of Mexitlia – Mexitlia altima –are newly described. Mallos ghiggi (Caporiacco, 1938) is considered a synonym of Mexitlia grandis (O. Pickard-Cambridge, 1896). Mexitlia grandis is considered the senior synonym of Mexitlia avara (Banks, 1898). Two species, Mallos jlavovittatus (Keyserling, 1880) and Mallos nigrescens (Caporiacco, 1955) are removed from Mallos. The males of Mallos kraussi Gertsch, 1946 and Mallos blandus Chamberlin and Gertsch 1958, are described for the first time. A cladistic analysis based on 26 morphological characters produced a cladogram that supports the monophyly of Mallos and the validity of Mexitlia. This cladogram presents a phylogenetic framework for considering the evolution of social behaviour in Mallos.  相似文献   

14.
15.
The spider genus Tayshaneta is revised based on results from a three gene phylogenetic analysis (Ledford et al. 2011) and a comprehensive morphological survey using scanning electron (SEM) and compound light microscopy. The morphology and relationships within Tayshaneta are discussed and five species-groups are supported by phylogenetic analyses: the anopica group, the coeca group, the myopica group, the microps group and the sandersi group. Short branch lengths within Tayshaneta contrast sharply with the remaining North American genera and are viewed as evidence for a relatively recent radiation of species. Variation in troglomorphic morphology is discussed and compared to patterns found in other Texas cave invertebrates. Several species previously known as single cave endemics have wider ranges than expected, suggesting that some caves are not isolated habitats but instead form part of interconnected karst networks. Distribution maps are compared with karst faunal regions (KFR's) in Central Texas and the implications for the conservation and recovery of Tayshaneta species are discussed. Ten new species are described: Tayshaneta archambaultisp. n., Tayshaneta emeraldaesp. n., Tayshaneta fawcettisp. n., Tayshaneta grubbsisp. n., Tayshaneta madlasp. n., Tayshaneta oconnoraesp. n., Tayshaneta sandersisp. n., Tayshaneta sprouseisp. n., Tayshaneta vidriosp. n. and Tayshaneta whiteisp. n. The males for three species, Tayshaneta anopica (Gertsch, 1974), Tayshaneta devia (Gertsch, 1974) and Tayshaneta microps (Gertsch, 1974) are described for the first time. Tayshaneta furtiva (Gertsch, 1974) and Tayshaneta uvaldea (Gertsch, 1974) are declared nomina dubia as the female holotypes are not diagnosable and efforts to locate specimens at the type localities were unsuccessful. All Tayshaneta species are thoroughly illustrated, diagnosed and keyed. Distribution maps are also provided highlighting areas of taxonomic ambiguity in need of additional sampling.  相似文献   

16.
17.
The non-mimetic Afrotropical spider genus Cambalida Simon, 1909, placed within a subfamily of predominantly ant-mimicking spiders (Araneae: Corinnidae: Castianeirinae), is revised. Three species are transferred from Castianeira Keyserling, 1879 to Cambalida: Cambalida deminuta (Simon, 1909), comb. n., Cambalida fulvipes (Simon, 1896), comb. n. and Cambalida loricifera (Simon, 1885), comb. n.. A fourth species, Cambalida fagei (Caporiacco, 1939), comb. n., is transferred from Brachyphaea Simon, 1895 to Cambalida. Two species, Castianeira depygata Strand, 1916, syn. n. and Cambalida mestrali Lessert, 1921, syn. n., are considered junior synonyms of Cambalida fulvipes. The males of Cambalida deminuta and Cambalida loricifera are redescribed and their unknown females are described for the first time. The female and male of Cambalida fulvipes and Cambalida coriacea Simon, 1909 are also redescribed. The type material of the type species of the genus, Cambalida insulana Simon, 1909 from Pagalu (Annobon) Island, is lost, and only immature specimens have been subsequently collected from a nearby island. The species is regarded as a nomen dubium until fresh adult material can be collected. A replacement name, Cambalida simoni nom. n. is proposed for Cambalida fulvipes Simon, 1909, the latter being a secondary junior homonym of Cambalida fulvipes (Simon, 1896). The type material of this species is also lost and it is too considered nomen dubium. The following new species are described: Cambalida compressa sp. n. from West Africa, Cambalida dippenaarae sp. n. from southern Africa, Cambalida griswoldi sp. n. and Cambalida lineata sp. n. from Madagascar, and Cambalida unica sp. n. from Cameroon. Notes are provided on the biology of each species and the distribution of the genus in the Afrotropical Region.  相似文献   

18.
In animals, supernumerary chromosomes and their evolution have mostly been studied in sexual reproducing species. In the present study, for the first time, the natural distribution and stability of supernumerary microchromosomes were investigated in the unisexual fish species Poecilia formosa. Natural habitats throughout the range of P. formosa were screened for the presence of microchromosomes over several years. A high frequency of microchromosomes was found in the Río Purificación river system. Evidence points to the presence of the same microchromosome lineage over many generations. No supernumerary chromosomes were found elsewhere than in the Río Purificación representing a significant difference in the distribution of microchromosome-bearing individuals between the Río Purificación and all other collection sites.  相似文献   

19.
A new species of recluse spider, Loxosceles niedeguidonaesp. n., is described from the Parque Nacional Serra da Capivara, State of Piauí, Brazil. This is the first endemic species described from Brazilian semi-arid environment. The species is included in gaucho group of Gertsch (1967) due to its spermathecal shape and is considered close to Loxosceles chapadensis Bertani, Fukushima & Nagahama, 2010 by the unusual long male palpal tibia, a character not common for species of this group. An updated key for Loxosceles species of gaucho group is presented.  相似文献   

20.
Wang MF  Li K  Zhang D 《ZooKeys》2011,(112):1-19
The Chinese fauna of the Fannia postica-group Chillcott (1961) is reviewed, the diagnostic features of this group are redefined, one new species, Fannia nudifemoratasp. n., is described, and a key to the males of nine known species is given. One new junior synonym, Fannia tigripeda Xue, Wang&Li, syn. n. for Fannia stigi Rognes is established. To facilitate comparisons of the species, Fannia aethiops Malloch, Fannia ardua Nishida, Fannia discoculea Xue, Fannia ringdahlana Collin, Fannia postica (Stein), Fannia spathiophora Malloch, and Fannia stigi Rognes are redescribed and illustrated. The geographic distribution of the known Chinese species is updated.  相似文献   

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