Displaying publications 1 - 20 of 1782 in total

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  1. Ng YF
    Zootaxa, 2015;4032(2):246-50.
    PMID: 26624359 DOI: 10.11646/zootaxa.4032.2.13
    Amalothrips noorazlani sp. n. is described from Malaysia based on both sexes, and a key is provided to the species of this genus. This is the first record of Amalothrips species outside India, and the first description of a male Amalothrips. The male has a pair of drepanae, the tergal posteromargin bears a toothed craspedum, but there are no sternal pore plates.
    Matched MeSH terms: India
  2. Kluge NJ, Selvakumar C, Sivaramakrishnan KG, Jacobus LM
    Zootaxa, 2015;4028(2):287-95.
    PMID: 26624311 DOI: 10.11646/zootaxa.4028.2.8
    We consider the genus Janohyphella Selvakumar, Sivaramakrishnan & Jacobus, 2014 (Ephemeroptera:Teloganodidae) to be a new junior synonym of Teloganella Ulmer, 1939 [=Janohyphella, syn. n.] based on comparative examination of new and previously studied materials from Malaysia and India. Thus, we propose the following new combination, Teloganella indica, comb. n., and provide new or modified diagnoses for this species, T. umbrata Ulmer, 1939 and the genus Teloganella Ulmer, 1939.
    Matched MeSH terms: India
  3. Von Schimonsky DM, Bichuette ME, Mahnert V
    Zootaxa, 2014;3889(3):442-6.
    PMID: 25544278 DOI: 10.11646/zootaxa.3889.3.6
    The small pseudoscorpion family Pseudochiridiidae Chamberlin, 1923 comprises two genera and 12 extant species recorded from Asia (Burma, Christmas Island, Indonesia, India, Nepal, Malaysia, New Guinea, Philippines, Nicobars and Sumba), eastern, central and southern Africa (Chad, D.R. Congo, Kenya, South Africa, Tanzania), Madagascar, Seychelles (Aldabra), North America (Florida) and the Caribbean Islands of Dominican Republic and Cuba (Harvey 2013, Barba & Barroso 2013); one unidentified species is mentioned for the fauna of Mexico (Ceballos 2004). A fossil species has been described from Dominican amber by Judson (2007), who predicted the presence of this family in South America. 
    Matched MeSH terms: India
  4. Hajong SR
    Zootaxa, 2014;3878(3):298-300.
    PMID: 25544448 DOI: 10.11646/zootaxa.3878.3.5
    The genus Lichnofugia is reported for the first time from India with a description of Lichnofugia umshingensis sp. nov. from Shillong, Meghalaya. The distribution of Lichnofugia thus extends eastward from Peninsular Malaysia and Thailand to north- eastern India.
    Matched MeSH terms: India
  5. Stehlík JL, Kment P
    Zootaxa, 2014;3860(2):167-83.
    PMID: 25283198 DOI: 10.11646/zootaxa.3860.2.4
    Riegeriana gen. nov. is described to accommodate Physopelta apicalis Walker, 1873. A lectotype of Ph. apicalis is de-signated. Iphita fasciata Stehlík & Jindra, 2008, syn. nov., is recognized as a new junior subjective synonym of Riegeriana apicalis. In addition, Iphita lata sp. nov. is described from southern India and a check-list of the species of the genus Iphita Stål, 1873 is provided. The etymology of Iphita nigris Ahmad & Abbas, 1992 and the lectotype designation of Dindymellus coimbatorensis Distant, 1919 are discussed. The following new or confirmed country records are provided: Iphita coimbatorensis (Distant, 1919) from India (Karnataka, Orissa); I. dubia (Breddin, 1901) from Indonesia (Papua); I. limbata Stål, 1870 from Cambodia, China (Hainan), India (Arunachal Pradesh), Indonesia (Sumatra, Kalimantan), Malaysia (Pahang: Tioman Island), and Vietnam; I. lycoides (Walker, 1873) from the Philippines (Panay Island). 
    Matched MeSH terms: India
  6. Lü L, Zhou HZ
    Zootaxa, 2015;3992(1):1-94.
    PMID: 26250256 DOI: 10.11646/zootaxa.3992.1.1
    Oxytelus species are widespread over all continents except Antarctica. Southeast Asia is one of the biodiversity hotspots in the world. In this paper, we review the Oxytelus species currently known from Southeast Asia. Seven species are described as new to science: O. castaneus sp. nov. (Vietnam), O. finitimus sp. nov. (Laos), O. grandiculus sp. nov. (Malaysia, Indonesia, and Thailand), O. insulanus sp. nov. (Malaysia and Indonesia), O. lompobatangensis sp. nov. and O. poecilopterus sp. nov. (Indonesia), and O. sublividus sp. nov. (Vietnam and Laos). Seven new synonymies are proposed: O. ruptus Fauvel = O. sublucidus Cameron, O. lucens Bernhauer = O. malaisei Scheerpeltz, O. puncticeps Kraatz = O. (Anotylus) micantoides Scheerpeltz, O. subferrugineus Cameron = O. kedirianus Cameron, O. megaceros Fauvel = O. kalisi Bernhauer, O. subincisus Cameron = O. fruhstorferi Cameron, O. antennalis Fauvel = O. cheesmani Bernhauer. Lectotypes are designated for the following names: O. armiger Fauvel, O. bellicosus Fauvel, O. discalis Cameron, O. gigantulus Fauvel, O. ginyuenensis Bernhauer, O. javanus Cameron, O. kalisi Bernhauer, O. kedirianus Cameron, O. lucens Bernhauer, O. lucidulus Cameron, O. mandibularis Cameron, O. megaceros Fauvel, O. nilgiriensis Cameron, O. subferrugineus Cameron, O. subincisus Cameron, O. sublucidus Cameron, O. subsculptus Cameron, O. antennalis Fauvel (New Caledonia, New Guinea and Australia), O. cheesmani Bernhauer (New Hebrides), O. cheesmanianus Cameron (Papua New Guinea), O. hingstoni Cameron (India), and O. tibetanus Bernhauer (China). The species O. (Anotylus) transversipennis Scheerpeltz is transferred to the genus Anotylus. Other than the new species, nine previously known species are redescribed, a key to 30 species and line drawings or color photographs of 42 species are provided. Thus, a total of 30 species are recorded from Southeast Asia.
    Matched MeSH terms: India
  7. Rognes K
    Zootaxa, 2015;3952(1):1-80.
    PMID: 25947832 DOI: 10.11646/zootaxa.3952.1.1
    The Oriental, Australasian and Oceanian genus Caiusa Surcouf, 1920 is revised, species concepts being based on male and female genitalia. A key to males for all known species, and a key to females for all except one are given. All relevant types still in existence have been studied, complete synonymies given and the geographical distribution reconsidered. The eight species included in the genus are: Caiusa borneoensis sp. nov. (Malaysia, Thailand, Vietnam); Caiusa coomani Séguy, 1948 (China, Malaysia, Singapore, Thailand, Vietnam); Caiusa indica Surcouf, 1920 (Australia, Cambodia, India, Indonesia, Malaysia, Papua New Guinea, Philippines, Singapore, Solomon Islands, Sri Lanka, Thailand, Vietnam); Caiusa karrakerae sp. nov. (Malaysia, Thailand); Caiusa kurahashii sp. nov. (Indonesia, Japan, Philippines); Caiusa pooae sp. nov. (Thailand); Caiusa testacea Senior-White, 1923 (India, Nepal, Sri Lanka) and Caiusa violacea Séguy, 1925, stat. rev. (Cambodia, China, Laos, Malaysia, Taiwan, Thailand, Vietnam). A lectotype is designated for Caiusa indica to fix the interpretation of the name. Caiusa nigronitens Senior-White, 1923, syn. nov. and Caiusa surcoufi Bezzi, 1927, syn. nov. are established as junior synonyms of Caiusa indica. Caiusa violacea is correctly diagnosed and errors in the original description of the female holotype are pointed out. Caiusa dubiosa Villeneuve, 1927 is established as a junior synonym of C. violacea, syn. nov. Seven Caiusa species have been reared from the egg mass of various species of frogs. The reproductive mode of the eighth species, i.e., C. indica, is unknown. Five species, i.e., C. borneoensis, C. coomani, C. karrakerae, C. kurahashii and C. violacea have been reared from one or more of the foam nesting frog species Chiromantis nongkhorensis (Cochran, 1927), Polypedates leucomystax (Gravenhorst, 1927), Polypedates megacephalus Hallowell, 1861, Rhacophorus annamensis Smith, 1924, Rhacophorus dulitensis Boulenger, 1892, Rhacophorus kio Ohler & Delorme, 2005 and Rhacophorus owstoni (Stejneger, 1907) all belonging in the family Rhacophoridae in Anura. These five Caiusa species all have a specialised ovipositor tip, with small spine-like setae on the ST8 and the hypoproct, probably enabling the flies to oviposit on a foam nest with a hardened outer surface. They form a monophyletic group on account of these features of the ovipositor, unique in the Oestroidea. The sixth species, C. testacea, has been reared from a frog egg mass, the frog species being unknown. Its ovipositor structure is also unknown. The seventh species, C. pooae, has been reared once from the jelly-like egg mass of Feihyla hansenae (Cochran, 1927), also in Rhacophoridae. Caiusa pooae females do not have spine-like setae on the ovipositor, a fact correlated with the soft outer surface of the jelly-like egg mass on which a C. pooae female had oviposited. The extreme rarity of C. pooae oviposition on Feihyla hansenae egg masses may indicate that this fly perhaps has another, unknown, regular oviposition substrate. Caiusa pooae and C. indica make up a second monophyletic group within Caiusa. Caiusa indica, the most common and most widespread species of the genus, has an ovipositor structure similar to C. pooae. Its breeding substrate is unknown and it occurs both within and outside the distributional area of Rhacophoridae. Possibly both C. indica and C. pooae share a regular oviposition substrate that has still to be discovered. The holotype female of Plinthomyia emimelania Rondani, 1875 from Sarawak is established as a member of the genus Bengalia Robineau-Desvoidy, 1830, thus Plinthomyia Rondani, 1875 becomes a junior synonym of Bengalia Robineau-Desvoidy, 1830, syn. nov. It is removed from the synonymy of Phumosia Robineau-Desvoidy, 1830.
    Matched MeSH terms: India
  8. Schmidt-Rhaesa A, Limatemjen L, Yadav AK
    Zootaxa, 2015;3925(1):202-10.
    PMID: 25781739 DOI: 10.11646/zootaxa.3925.2.3
    The currently known diversity of horsehair worms (Nematomorpha) from India is only 17 species. We report here two female specimens found on two occasions on a terrace paddy field in Tsupo, Viswema, Kohima, Nagaland, India. Although found at the same location, both species differ in their cuticular structures. One is determined as Chordodes moutoni, a species known from China, Malaysia and India. The other specimen shows a new type of cuticular structure, the areoles, which combines characters of both simple areoles and tubercle areoles. This specimen is described as a new species, C. combiareolatus. Both specimens show arrangements on the cuticle, in which a circle of areoles surrounds a region of "naked" cuticle. We interpret these regions as artifacts caused by the breaking off of the central crowned areoles, leaving only the circumcluster areoles behind.
    Matched MeSH terms: India
  9. Viraktamath CA, Webb MD, Yeshwanth HM
    Zootaxa, 2021 Jan 25;4915(4):zootaxa.4915.4.1.
    PMID: 33756549 DOI: 10.11646/zootaxa.4915.4.1
    One new genus of the tribe Ledrini, Yelahanka gen. nov. is described with Petalocephala granulosa Distant as its type species. The genus is characterised by the flexing of the forewing laterad of a strongly carinate or keeled outer claval vein and the claval veins fused in the distal two thirds. Seven new species, Yelahanka canaraica sp. nov. (India: Karnataka), Y. kodaiensis sp. nov. (India: Tamil Nadu), Y. montana sp. nov. (India: Tamil Nadu), Y. nepalica sp. nov. (Nepal), Y. sikkimensis sp. nov. (India: Sikkim), Y. shillongensis sp. nov. (India: Meghalaya) and Y. trifida sp. nov. (India: Himachal Pradesh, Arunachal Pradesh) are described and illustrated. The following new combinations are proposed: Yelahanka bainbriggei (Distant) comb. nov., Y. granulosa (Distant) comb. nov., Y. punctata (Walker) comb. nov. and Y. tabulata (Distant) comb. nov.; originally punctata was placed in the genus Ledra Fabricius and remaining species were placed in Petalocephala Stål. Petalocephala bainbriggei Distant 1916 is treated as a junior synonym of Y. granulosa (Distant 1910) syn. nov. and P. tabulata Distant 1908 is treated as a junior synonym of Yelahanka punctata (Walker 1851) syn. nov. Y. granulosa is newly recorded from Africa (Tanzania and Kenya) and Malaya. Relationships of the new genus with other genera of Ledrini are discussed and a key to species of the genus is also provided.
    Matched MeSH terms: India
  10. Salini S, Kment P
    Zootaxa, 2021 Apr 14;4958(1):zootaxa.4958.1.31.
    PMID: 33903478 DOI: 10.11646/zootaxa.4958.1.31
    The genus Surenus Distant, 1901 (Hemiptera: Heteroptera: Pentatomoidea: Pentatomidae: Pentatominae: Halyini) is revisited and found to be a junior subjective synonym of the genus Agathocles Stål, 1876 (currently Pentatominae: Rolstoniellini). The genus Agathocles and its type species, Agathocles limbatus Stål, 1876, are redescribed. Lectotype of Surenus normalis Distant, 1901 (= Agathocles normalis (Distant, 1901) comb. nov.) is designated and the unknown male of the species is described. Agathocles yunnanensis Zhang Lin, 1984, syn. nov., is considered junior subjective synonym of A. limbatus. Two new species are described: Agathocles flavipes sp. nov. from India (Andhra Pradesh, Karnataka, Maharashtra, and Tamil Nadu) and A. joceliae sp. nov. from Malaysia (Kelantan, Perak). The new species differ from their congeners mainly by the morphology of mandibular plates, length of antennomeres I, IIa and IIb, body length, and structure of male genitalia. Agathocles dubius Distant, 1921 is transferred to the genus Caystrus Stål, 1861 (Pentatominae: Caystrini) based on examination of its holotype with the resulting new combination: Caystrus dubius (Distant, 1921), comb. nov. One new combination is proposed, Paramecocoris ruficornis (Fieber, 1851), comb. nov. (from preoccupied Paramecus Fieber, 1851), and its type locality is clarified as Tenasserim (south Myanmar). Gender agreement and authorship of the name Riazocoris niger Ahmad Afzal, 1977 in Ahmad et al. (1977: 161) are corrected and status of its name bearing type is clarified as lectotype. The following new distribution records are given: A. limbatus from Cambodia, China (Guangxi, Tibet), Laos and Thailand, A. normalis, Caystrus obscurus (Distant, 1901a) and Critheus lineatifrons Stål, 1869 from Laos, Amasenus corticalis Stål, 1863 from Cambodia, Indonesia (E Kalimantan), Laos, Myanmar and Thailand, and Rolstoniellus boutanicus (Dallas, 1849) from Vietnam. Based on characters of external morphology and genitalia, the genus Agathocles is compared with representatives of the genera Halys Fabricius, 1803 (Halyini), Caystrus (Caystrini), Laprius Stål, 1861 (Myrocheini), and Exithemus Distant, 1902 (currently in Rolstoniellini). As a result, the genus Agathocles is here transferred to the tribe Caystrini. The genus Kyrtalus Van Duzee, 1929 is tentatively placed in Myrocheini based on the presence of sulcate mesosternum and femora provided with teeth.
    Matched MeSH terms: India
  11. Joshi R, Kirti JS, Singh N
    Zootaxa, 2016 Oct 28;4179(1):128-132.
    PMID: 27811698 DOI: 10.11646/zootaxa.4179.1.10
    Genus Nishada Moore (1878) was proposed as a monotypic genus, under subfamily Lithosiinae, family Lithosiidae (now Lithosiini), including only Nishada flabrifera Moore (1878) from Calcutta (now as Kolkata), India. The genus is distributed from China to India, Thailand, Malaysia and up to Australia. The Indian fauna of Nishada is reported from North-East Himalayas, West Bengal (Kolkata) and South India. Members of this genus are unmarked, yellow to brown with short and broad wings. Genus Nishada has been taxonomically dealt by many authors but awaits thorough revision.

    HISTORY: Hampson (1900) included a total of ten species: Nishada niveola Hampson, 1900, Nishada syntomioides (Walker, 1862), Nishada impervia (Walker, 1865), Nishada marginalis (Felder 1875), Nishada tula Swinhoe, 1900, Nishada nodicornis (Walker 1862), Nishada rotundipennis (Walker 1862), Nishada flabrifera Moore, 1878, Nishada sambara (Moore 1859) and Nishada xantholoma (Snellen 1879). Swinhoe (1902) and Hampson (1911) then described two new species, Nishada melanistis and Nishada brunneipennis, respectively, followed by Rothschild (1912, 1913) who described a further seven new species, Nishada brunnea, Nishada flavens, Nishada testacea, Nishada griseoflava, Nishada fuscofascia, Nishada louisiadensis and Nishada aurantiaca, bringing the total to 19 species. Strand (1922) catalogued only 13 of these species in Nishada, transferring N. brunnea and N. fuscofascia to genus Scoliacma Meyrick (1886); N. testacea, N.griseoflava and N. louisiadensis Rothschild to Eilema Hübner (1819) and synonymising N. flavens with N. sambara. Next, Matsumura (1927) described N. formosibia, followed by two more species, N. aureocincta Debauche, 1938 and N. benjaminea Roepke, 1946. Holloway (2001) synonymised N. nodicornis with N. rotundipennis and added the description of a new subspecies, Nishada chilomorpha adunca Holloway, 2001 from Borneo, indicating a distributional range as far as North East India. The nominotypical subspecies, N. c. chilomorpha was suggested to be restricted to its type locality of Java. Bucsek (2012) added Nishada cameronensis, Dubatolov & Bucsek (2013) described Nishada schintlmeisteri and Bucsek (2016) described Nishada temenggora. So, at present, Nishada comprises19 species, of which three are known from India (Singh et al. 2014). Herein, we describe one further species, Nishada pseudochilomorpha Joshi & Singh sp. nov., from Jatinga (Assam, India). In addition, new distributional records are reported for N. flabrifera.

    Matched MeSH terms: India
  12. Manickavasagam S, Triapitsyn SV, Palanivel S
    Zootaxa, 2018 Feb 26;4387(1):134-156.
    PMID: 29690489 DOI: 10.11646/zootaxa.4387.1.6
    An overview of the Oriental species of Cleruchus Enock (Hymenoptera: Mymaridae) is given, and its five newly described species as well as one undescribed species from Malaysia are keyed. The described new taxa are C. funiculatus Manickavasagam Palanivel sp. n., C. indicus Manickavasagam Palanivel sp. n. and C. orientalis Manickavasagam Palanivel sp. n., all from India, C. blimp Triapitsyn sp. n. from Brunei, and C. pmilb Triapitsyn sp. n. from Thailand. Anaphes quinquearticulatus Huber Triapitsyn is newly reported from India.
    Matched MeSH terms: India
  13. JaŁoszyŃski P
    Zootaxa, 2018 Mar 20;4399(1):141-145.
    PMID: 29690338 DOI: 10.11646/zootaxa.4399.1.12
    Clidicus Laporte, 1832 currently comprises 27 species distributed in India (Karnataka, Tamil Nadu), Sri Lanka, Indonesia (Java, Kalimantan, Sumatra), Malaysia (Sabah, Sarawak), Laos, Vietnam, the Philippines (Mindanao), China (Hainan) and Australia (Queensland). Some species have conspicuously large adults reaching 8.5 mm, and they represent the largest known Scydmaeninae. Species of Clidicus were relatively poorly known until recently, when Orousset (2014) revised a large portion of this genus and described several new species. Other major studies include Besuchet (1971), who described Sri Lankan species, Jałoszyński et al. (2003) who recorded four new species from Vietnam and Laos, Jałoszyński (2009) with the first description of a Philippine species, and Zhou Li (2015), who discovered the first species in China. Another new species, representing the second Clidicus occurring in the Philippines, is described below.
    Matched MeSH terms: India
  14. Vilkamaa P, Rudzinski HG, BurdÍkovÁ N, ŠevČÍk J
    Zootaxa, 2018 Mar 21;4399(2):248-260.
    PMID: 29690308 DOI: 10.11646/zootaxa.4399.2.8
    Four Oriental species of Aerumnosa Mohrig, 1999 (Diptera: Sciaridae), a genus previously known only from Papua New Guinea, are newly described and illustrated: Aerumnosa bituberculata sp. n. (India), A. gemmifera sp. n. (Malaysia: Sabah), A. horrifica sp. n. (Brunei, Thailand) and A. impar sp. n. (Malaysia: Sabah). On the basis of the new material, the genus is redefined. A key to the known species of Aerumnosa is presented, including four new species. An updated molecular phylogenetic analysis based on four gene markers (18S, 28S, 16S and COI) shows Aerumnosa to be a member of the subfamily Cratyninae. The monophyly of Cratyninae is well supported, which clade also includes the genera Hyperlasion Schmitz, 1919, Pnyxiopalpus Vilkamaa Hippa, 1999 and Pseudoaerumnosa Rudzinski, 2006. According to the present phylogenetic hypothesis, the monophyly of Cratyna Winnertz, 1967 s. l. needs to be revisited. The clade including Cratyna (s. str.) ambigua (Lengersdorf, 1934) appears as the sister group of Aerumnosa.
    Matched MeSH terms: India
  15. Selis M
    Zootaxa, 2018 Apr 05;4403(3):441-468.
    PMID: 29690217 DOI: 10.11646/zootaxa.4403.3.2
    New additions to the knowledge of the subfamily Eumeninae are provided. Eight new species of Eumeninae are described: Antepipona gibbosissima Selis, sp. nov. (Namibia: Warmbad); Antepipona tricolorata Selis, sp. nov. (India: Sikkim); Ectopioglossa luzonica Selis, sp. nov. (Philippines: Luzon); Lissodynerus unicus Selis, sp. nov. (India: Sikkim); Pararrhynchium aurigaster Selis, sp. nov. (Malaysia: Johor); Symmorphus (Symmorphus) incisus Selis, sp. nov. (India: Sikkim); Symmorphus (Symmorphus) palawanensis Selis, sp. nov. (Philippines: Palawan); Zethus (Zethus) intermedius Selis, sp. nov. (Burkina Faso). The male of Synagris (Paragris) biplagiata Gusenleitner, 2005 is described. New distributional data for other species are provided.
    Matched MeSH terms: India
  16. Wu C, Yang Z, Liu CX, Zong C
    Zootaxa, 2017 Dec 20;4365(5):585-589.
    PMID: 29686191 DOI: 10.11646/zootaxa.4365.5.5
    The genus Molpa Walker was previously considered to be disjunctly distributed in broad-leaf rain forests in India and Malaysia. Here we report one new species Molpa dulongensis sp. nov. from subtropic broad-leaf rain forests in southwestern Yunnan Province in China. This is a part of the Indo-Burma biodiversity hotspot area. So we can infer that Molpa is continuously distributed in broad-leaf rain forests found in Oriental Region. Redescription of the genus Molpa and description of the new species Molpa dulongensis sp. nov. are provided. The types are deposited in Insect Collection of Institute of Zoology, Chinese Academy of Sciences, Beijing, China (IZCAS).
    Matched MeSH terms: India
  17. Lee CF
    Zootaxa, 2017 05 19;4269(1):1-43.
    PMID: 28610338 DOI: 10.11646/zootaxa.4269.1.1
    The genus Doryscus Jacoby, 1887 is revised. Twelve new species are described: D. indochinensis sp. nov. from China (Yunnan), India, Laos, Thailand, Vietnam; D. krausi sp. nov. from Laos and Thailand; D. kubani sp. nov., from China (Yunnan); D. geiseri sp. nov. from Singapore and Thailand; D. nepalensis sp. nov. from Bhutan, north India, and Nepal; D. luzonensis sp. nov., and D. mindanaoensis sp. nov. from Philippines; D. barclayi sp. nov., D. boreri sp. nov., D. javanensis sp. nov., and D. sumatrensis sp. nov. from Indonesia; D. wangi sp. nov. from East Malaysia (Sabah). Doryscus chujoi Takizawa, 1978 and D. varians (Gressitt & Kimoto, 1963) are removed from synonymy with D. testaceus Jacoby, 1887. Doryscus nigricollis Jiang, 1992 and D. marginicollis Jiang, 1992 are regarded as junior synonyms of D. varians (Gressitt & Kimoto, 1963). A lectotype is designated for Doryscus testaceus Jacoby, 1887.
    Matched MeSH terms: India
  18. Tanasevitch AV
    Zootaxa, 2017 Feb 03;4227(3):zootaxa.4227.3.2.
    PMID: 28187572 DOI: 10.11646/zootaxa.4227.3.2
    Linyphiid spiders collected from the Indo-Malayan Region and kept at three European Museums are studied. Twenty-three known species are newly recorded from continental or insular parts of Southeastern Asia and from the Oriental area of India. Seven new species are described: Asiagone komannai n. sp. (from Thailand), Erigone apophysalis n. sp. and E. sumatrana n. sp. (Sumatra, Indonesia), Gnathonarium luzon n. sp. (Philippines), Ketambea acuta n. sp. (Thailand, Myanmar), Oedothorax myanmar n. sp. (Myanmar) and Theoa malaya n. sp. (West Malaysia).
    Matched MeSH terms: India
  19. Muhammad AA, Tan MK, Abdullah NA, Azirun MS, Bhaskar D, Skejo J
    Zootaxa, 2018 Sep 25;4485(1):1-70.
    PMID: 30313773 DOI: 10.11646/zootaxa.4485.1.1
    Pygmy grasshoppers (Tetrigidae) are a speciose group of complicated taxonomy, with many species requiring clarification on their species boundaries, and more still awaiting discovery. Two new species of Scelimena Serville, 1838 are described: (1) from S. discalis species group S. gombakensis sp. nov. and (2) from S. hexodon species group Scelimena marta sp. nov. Catalogue of Scelimenini genera (15) and species (100) is presented and taxonomy and biogeography of the tribe are discussed. New and resurrected combinations are: Falconius becvari (Buzzetti Devriese, 2008) comb. nov. (of Gavialidium becvari), Gavialidium carli Hebard, 1930 comb. resurr. (of Bidentatettix carli), Indoscelimena india (Hancock, 1907) comb. nov. (of Scelimena india), Paragavialidium nodiferum (Walker, 1871) comb. nov. (of Platygavialidium nodiferum), Platygavialidium productum (Walker, 1871) comb. nov. (of Gavialidium productum), Scelimena hexodon (Haan, 1843) comb. resurr. (of Hexocera hexodon), Scelimena rosacea (Hancock, 1915) comb. resurr. (of Amphibotettix rosaceus), Tegotettix bufocrocodil (Storozhenko Dawwrueng, 2015) comb. nov. (of Gavialidium bufocrocodil). New synonyms are: Gavialidium phangensum Mahmood, Idris Salmah, 2007 syn. nov. (of Eufalconius pendleburyi), Gavialidium philippinum Bolívar, 1887 syn. nov. (of Platygavialidium productum comb. nov.), Hexocera Hancock, 1915 syn. nov. (of Scelimena), Paracriotettix Liang, 2002 syn. nov. (of Scelimena), Paracriotettix zhengi Liang, 2002 syn. nov. (of Scelimena melli), Scelimena mellioides Deng, 2016 syn. nov. (of Scelimena melli), Scelimena wuyishanensis Deng, 2016 syn. nov. (of Platygavialidium sinicum). The genus Scelimena is divided into six species groups. Eucriotettix neesoon Tan Storozhenko nom. nov. is new name for homonym Eucriotettix guentheri Tan Storozhenko, 2017. Finally, a tabular key to 15 Scelimenini genera, based on 16 morphological characters, is presented.
    Matched MeSH terms: India
  20. Casale A, Shi H
    Zootaxa, 2018 Jun 29;4442(1):1-42.
    PMID: 30313981 DOI: 10.11646/zootaxa.4442.1.1
    This revision focuses on the genus Calleida Latreille, 1824 (in the widest sense) in the Oriental Region, previously treated as genus or subgenus Callidiola Jeannel, 1949. In the present contribution, as first part of a series of revisions of the Asiatic Calleida species, we define nine species groups including all known Asiatic species, based on external features and morphological characters of male and female genitalia. A key for the identification of all nine species groups is provided, along with diagnostic characters, included species, geographical distribution, and brief discussion on monophyly and relationships for each species group. In particular, the present contribution deals with species of six small species groups, including eleven species in total, for which keys to all known species, descriptions, distribution maps, habitus images and genitalia illustrations are provided.Five new species are described: Calleida gressittiana Casale Shi, sp. n. (type locality: Kinabalu, Sabah, Borneo), Calleida puncticollis Shi Casale, sp. n. (type locality: Zigui, Hubei), Calleida jelineki Casale Shi, sp. n. (type locality: Coimbatore, India), Calleida viet Casale Shi, sp. n. (type locality: Vung Tau, Vietnam), Calleida borneensis Shi Casale, sp. n. (type locality: Sabah, Borneo). Lectotypes for five taxa are designated. One synonymy is newly proposed: Calleida lieftincki Louwerens junior synonym of Calleida corporaali Andrewes, syn. nov.
    Matched MeSH terms: India
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