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The fast-running flies (Diptera, Hybotidae, Tachydromiinae) of Singapore and adjacent regions
(2012)
This is the first comprehensive introduction to the flies of the subfamily Tachydromiinae (Hybotidae) of Singapore. The monograph summarizes all publications on the Tachydromiinae of Singapore and includes new data resulting from mass-trapping surveys made in Singapore during the last six years. A few samples from Malaysia (Johor province, Pulau Tioman and Langkawi) have been also included in this study. In Singapore the Tachydromiinae are the most diverse group of Empidoidea (except Dolichopodidae) and currently comprise 85 species belonging to the following nine genera: Platypalpus (1), Tachydromia (1), Chersodromia (6), Pontodromia (1), Drapetis (5), Elaphropeza (60), Crossopalpus (1), Nanodromia (3) and Stilpon (7). All species are diagnosed and illustrated. The following 28 species are described as new for science: Chersodromia bulohensis sp. nov. (Singapore), C. glandula sp. nov. (Singapore, Malaysia), C. malaysiana sp. nov. (Singapore, Malaysia), C. pasir sp. nov. (Malaysia), C. sylvicola sp. nov. (Singapore), C. tiomanensis sp. nov. (Malaysia), Crossopalpus temasek sp. nov. (Singapore), Drapetis bakau sp. nov. (Singapore, Malaysia), D. hutan sp. nov. (Singapore), D. laut sp. nov. (Singapore, Malaysia), D. mandai sp. nov. (Singapore), D. pantai sp. nov. (Singapore, Malaysia), Elaphropeza chanae sp. nov. (Singapore), E. collini sp. nov. (Singapore), E. gohae sp. nov. (Singapore), E. kranjiensis sp. nov. (Singapore), E. lowi sp. nov. (Singapore), E. semakau sp. nov. (Singapore), E. shufenae sp. nov. (Singapore), Nanodromia hutan sp. nov. (Singapore), N. spinulosa sp. nov. (Singapore), Platypalpus singaporensis sp. nov. (Singapore), Pontodromia pantai sp. nov. (Singapore), Stilpon arcuatum sp. nov. (Singapore), S. neesoonensis sp. nov. (Singapore), S. nigripennis sp. nov. (Singapore), S. singaporensis sp. nov. (Singapore), S. weilingae sp. nov. (Singapore). A redescription is given for Crossopalpus exul (Osten-Sacken, 1882) (Taiwan). Males of Elaphropeza feminata Shamshev & Grootaert, 2007 and E. modesta Shamshev & Grootaert, 2007 as well as females of Elaphropeza ubinensis Shamshev & Grootaert, 2007 and Nanodromia narmkroi Grootaert & Shamshev, 2003 are described for the first time. Keys to genera and species, which are generally applicable to the whole of Southeast Asia, are compiled. An analysis of the species ecological preferenda is presented.
The taxonomy of the family Desmodoridae (Nematoda: Desmodorida) is partially revised based on morphology. The diagnoses of the Desmodoridae and the subfamilies Desmodorinae and Spiriniinae are emended to accommodate re-analyzed morphological features. Eight known species are redescribed and the implication of the new findings for the taxonomy of the group is discussed. Amphispira and Metadesmodora are confirmed as genera inquirendae. Alaimonema and Sigmophoranema, and their corresponding type species, are proposed as inquirendae due to poor descriptions of the type material. The other three species of Sigmophoranema are transferred to the genus Onyx because they bear the diagnostic features of this group: spear-like dorsal tooth and s-shape precloacal supplements. Echinodesmodora, Paradesmodora and Stygodesmodora are transferred to the Spiriniinae based on the absence of a head capsule and on the amphidial fovea being surrounded by cuticle striation. Paradesmodora toreutes is transferred to the genus Acanthopharyngoides as A. toreutes comb. nov. The genus Onepunema does not fit in the family Desmodoridae because of diorchic males; thus, it is regarded as taxon incertae sedis.
Lists of valid genera for the two subfamilies are provided. A dichotomic key for the identification of the 14 genera within the Spiriinae is provided.
By taking Flavalona gen. nov. out of Alona s.l. (Cladocera: Anomopoda: Chydoridae), the last major clade has now been removed from this polyphyletic assemblage. Flavalona gen. nov. is a monophylum defined by having three, rarely two connected head pores and slit-shaped, rarely rounded lateral head pores. Postabdomen rather long, distally narrowed, with robust marginal denticles and weakly developed lateral fascicles of setules. End-claw weakly curved and with short basal spine. Male postabdomen with gonopores opening at the end of a penis-like outgrowth. Trunk limbs: exopodite of P2 with seta; inner portion of P4 with flaming-torch shaped setae; P5 with filter plate of three setae; P6 a large simple lobe. The relationship of the new genus with other Aloninae remains to be determined. A key to the 11 species of the genus is provided and a discussion of their geographic distribution and habitat type is given.
Two new species of Tetrastigma from Thailand, T. calcicola Kochaiph. & Trias-Blasi sp. nov. and T. jaichagunii C.L.Li ex Kochaiph. & Trias-Blasi sp. nov. are described and illustrated. Tetrastigma calcicola sp. nov. is a slender climber restricted to the open areas on limestone mountains at high elevation in the northern part of Thailand. The other species, T. jaichagunii sp. nov., is similar to T. harmandii Planch., but differs from it by having more densely verrucose young branches, broader leaflets, 4-lobed thick discs, bigger globose berries and oblongoid seeds. This species occurs along streams or in forest margins in evergreen forest and it is widely distributed in several parts of Thailand.
The Arabian Temnothorax Mayr, 1861 fauna is revised for the first time. Three species are recognized from the region: Temnothorax arabicus Sharaf & Akbar sp. nov., T. liviae (Agosti & Collingwood, 2011) comb. nov. and T. megalops (Hamann & Klemm, 1967). Leptothorax saudiae Collingwood & Agosti, 1996 was placed in Temnothorax by Bolton (2003), but actually belongs to Tetramorium Mayr, 1855 and is herewithin recombined to Tetramorium saudiae (Collingwood & Agosti, 1996) comb. nov. Automontage images and comparative diagnoses of workers as well as notes on habitats and distribution of treated species are provided. A revised key to the Arabian species based on the worker caste is also presented.
The genus Oxidus Cook, 1911 is revised to contain five species, O. avia (Verhoeff, 1937), O. gigas (Attems, 1953), O. gracilis (C.L. Koch, 1847), O. riukiaria (Verhoeff, 1940), and “species inquirenda” O. obtusus (Takakuwa, 1942). A cosmopolitan species, O. gracilis, is widely found in temperate and sub-tropical regions over the world, but other species have limited distribution in restricted regions, e.g., O. gigas in northern Vietnam, O. riukiaria and O. avia in the Ryukyu Islands (Japan). Four species, O. gracilis, O. riukiaria, O. avia and O. gigas, are confirmed as different from each other in gonopod characters, coloration and body size. The status of the last species, O. obtusus, is still doubtful and requires examination of further fresh material. The phylogenetic relationships among species of Oxidus is analyzed using two fragments of the mitochondrial genes COI (Cytochrome c Oxidase subunit I) and 16S rRNA. Three species of Oxidus are clearly separated from each other; O. gigas and O. gracilis form a monophyletic sister group with O. riukiaria. The genus Oxidus is also monophyletic and more closely related to the genus Tylopus Jeekel, 1968 than to the genera Sellanucheza Enghoff, Golovatch & Nguyen, 2004 or Kronopolites Attems, 1914. In addition, an identification key to species of Oxidus is provided.
Following a taxonomic revision of Begonia L. (Begoniaceae, Cucurbitales) from Northeast India based on 332 herbarium specimens, 38 species are confirmed to occur in the region, of which ten are endemic. One new species is described, Begonia koelzii R.Camfield sp. nov., in B. sect. Platycentrum (Klotzsch) A.DC. One species is reduced into synonymy; B. barbata Wall. is now a synonym of B. thomsonii A.DC. Three species, B. difformis (Irmsch.) W.C.Leong, C.I Peng & K.F.Chung, B. labordei H.Lév. and B. handelii Irmsch., are reported new for India, and B. lushaiensis C.E.C.Fisch. is reinstated as an accepted species, having previously been synonymised under B. modestiflora Kurz. A key to the species in the region and preliminary conservation assessments are presented.
The South American genus Phantasca Redtenbacher, 1906 (Phasmatodea: Diapheromeridae: Diapheromaerinae) is re-diagnosed and revised at the species level. The precedingly unknown eggs are described for the first time. The genus Pterolibethra Günther, 1940 (type species: P. heteronemia Günther, 1940) is re-synonymised, with Phantasca (syn. nov.) and consequently the two species originally contained, P. heteronemia Günther, 1940 and P. poeciloptera Günther, 1940, are transferred to Phantasca (comb. rev.). P. laeta Conle, Hennemann & Gutierréz, 2011 is not congeneric and is transferred to the genus Jeremiodes Hennemann & Conle, 2007 (Cladomorphinae: Cladomorphini; comb. nov.). Two species are removed from Bacteria Berthold, 1827 and transferred to Phantasca; these are B. quadrilobata Chopard, 1911 and B. montana Redtenbacher, 1906 (comb. nov.). Six new species are described: P. adiposa sp. nov., P. amabile sp. nov., P. femorata sp. nov., P. guianensis sp. nov., P. nigrolineata sp. nov. and P. ruboligata sp. nov. The male and egg of P. quadrilobata (Chopard, 1911) are described and illustrated for the first time. The genus now contains 13 species that are distributed throughout the northern half of South America. A key as well as detailed descriptions and illustrations are presented for all known species.
The new genus Neodiplopeltula gen. nov. is proposed to accommodate those species from the genus Diplopeltula Gerlach, 1950 that possess the following morphological characters: amphids in the shape of an elongated loop, a well-developed subcylindrical stoma and outstretched ovaries. The genus Diplopeltula is considered genus inquirendum et incertae sedis. Four species placed in Neodiplopeltula gen. nov. are redescribed. The following taxonomic changes are proposed: Neodiplopeltula asymmetrica (Allgén, 1935) gen. et comb. nov.; Neodiplopeltula barentsi (Steiner, 1916) gen. et comb. nov.; Neodiplopeltula bathmanni (Jensen, 1991) gen. et comb. nov.; Neodiplopeltula cuspidiboja (Leduc, 2017) gen. et comb. nov.; Neodiplopeltula indica (Gerlach, 1962) gen. et comb. nov.; Neodiplopeltula intermedia (Gerlach, 1954) gen. et comb. nov.; Neodiplopeltula obesa (Nguyen Vu Thahn, Nguyen Thahn Hien & Gagarin, 2012) gen. et comb. nov.; Neodiplopeltula onusta (Wieser, 1956) gen. et comb. nov.; Neodiplopeltula ovalis (Ditlevsen, 1928) gen. et comb. nov. and Neodiplopeltula tchesunovi (Fadeeva & Mordukhovich, 2013) gen. et comb. nov. New synonyms include: Diplopeltis asymmetricus Allgén, 1935 and Diplopeltis ovalis Ditlevsen, 1928 are synonimised with Neodiplopeltula barentsi (Steiner, 1916) gen. et comb. nov.; Diplopeltula tchesunovi Fadeeva & Mordukhovich, 2013 is synonimised with Neodiplopeltula onusta (Wieser, 1956) gen. et comb. nov.; the male of Diplopeltula cuspidiboja Leduc, 2017 is synonimised with Neodiplopeltula barentsi gen. et comb. nov. and the female with N. bathmanni gen. et comb. nov. A key to the species of Neodiplopeltula gen. nov. is provided.