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Four new species of Brueelia Kéler, 1936 are described and illustrated. All of them parasitize African endemic host species in the families Passeridae, Ploceidae, and Estrildidae (Passeriformes). They are: Brueelia pofadderensis sp. nov. ex Passer melanurus damarensis Reichenow, 1902 and P. m. vicinus Clancey, 1958; B. semiscalaris sp. nov. ex Granatina granatina (Linnaeus, 1758); B. sima sp. nov. ex Malimbus nitens (Gray, 1831); B. terpsichore sp. nov. ex Euplectes jacksoni (Sharpe, 1891) and E. progne delamerei (Shelley, 1903). In addition, Brueelia bicurvata (Piaget, 1880) is redescribed and reillustrated from non-type material. A summary of all published records of lice in the Brueelia complex from Africa since 1980 is provided. We also estimate the unknown diversity of African species of Brueelia based on an index of host specificity calculated for each host family independently. The unknown diversity is estimated to be over 1000 species of Brueelia from African hosts, compared to the < 50 species in this genus currently recorded from Africa.
Three new species of Thinophilus Wahlberg, 1844 are described from marine sites on the Andaman Sea coasts in peninsular Thailand: T. inaequalis Samoh & Grootaert sp. nov. belonging to the 'Thinophilus simplex-group' sensu Grootaert, 2018, T. plektron Samoh & Grootaert sp. nov., an unplaced species characterised by a long flattened apical spur on the hind tibia, and T. subapicalis Samoh & Grootaert sp. nov. belonging to the 'Thinophilus spinatus-group' sensu Grootaert, 2018. New records are given for following species occurring in peninsular Thailand: T. apicatus Grootaert, 2018, T. chaetulosus Grootaert, 2018, T. clavatus Zhu, Yang & Masunaga, 2006, T. evenhuisi Grootaert, 2018, T. lenachanae Grootaert, 2018, T. longicilia Evenhuis & Grootaert, 2002, T. nigrilineatus Grootaert, 2018, T. simplex Grootaert, 2018, T. superbus Grootaert, 2018, and T. yeoi Grootaert, 2018.
The Oriental species of the genus Sphegina Meigen, 1822 are revised. The following 43 new species are described: Sphegina (Sphegina) abbreviata sp. nov. (Nepal), S. (S.) angustata sp. nov. (Nepal), S. (Asiosphegina) albolobata sp. nov. (Vietnam), S. (Asiosphegina) amplistylus sp. nov. (Philippines), S. (A.) atrimanus sp. nov. (Vietnam), S. (A.) bifida sp. nov. (Sabah, Malaysia), S. (A.) bracon sp. nov. (Vietnam), S. (A.) brevipilis sp. nov. (China), S. (A.) clavigera sp. nov. (Vietnam), S. (A.) collicola sp. nov. (Malaysia), S. (A.) crinita sp. nov. (Java, Indonesia; Malaysia), S. (A.) dentata sp. nov. (Taiwan), S. (A.) distincta sp. nov. (Vietnam), S. (A.) exilipes sp. nov. (Java, Indonesia), S. (A.) farinosa sp. nov. (Sabah, Malaysia), S. (A.) fimbriata sp. nov. (Thailand), S. (A.) furcillata sp. nov. (Vietnam), S. (A.) ghatsi sp. nov. (India), S. (A.) gigantea sp. nov. (China), S. (A.) granditarsis sp. nov. (China), S. (A.) hamulata sp. nov. (India), S. (A.) hauseri sp. nov. (Nepal), S. (A.) incretonigra sp. nov. (Vietnam), S. (A.) inflata sp. nov. (Philippines), S. (A.) inventum sp. nov. (Sabah, Malaysia), S. (A.) karnataka sp. nov. (India), S. (A.) licina sp. nov. (Thailand), S. (A.) lobulata sp. nov. (Vietnam), S. (A.) lucida sp. nov. (Vietnam), S. (A.) nigrotarsata sp. nov. (Vietnam), S. (A.) nubicola sp. nov. (Thailand), S. (A.) ornata sp. nov. (China), S. (A.) perlobata sp. nov. (Taiwan), S. (A.) plautus sp. nov. (China), S. (A.) prolixa sp. nov. (Malaysia, Thailand), S. (A.) setosa sp. nov. (Nepal, India), S. (A.) spathigera sp. nov. (Philippines), S. (A.) spenceri sp. nov. (Vietnam), S. (A.) strigillata sp. nov. (Vietnam), S. (A.) taiwanensis sp. nov. (Taiwan), S. (A.) umbrosa sp. nov. (China), S. (A.) verrucosa sp. nov. (Vietnam) and S. (A.) vietnamensis sp. nov. (Vietnam). Sphegina. (A.) tenuis Brunetti, 1915 is not a synonym of S. (A.) javana de Meijere, 1914. The males of S. (A.) apicalis Shiraki, 1930, S. (A.) tricoloripes Brunetti, 1915 and S. (A.) varidissima Shiraki, 1930 and the females of S. (A.) achaeta Hippa, van Steenis & Mutin, 2015, S. (A.) index Hippa, van Steenis & Mutin, 2015, S. (A.) mirifica Hippa, van Steenis & Mutin, 2015 and S. (S.) quadriseta Huo & Ren, 2006 are described for the first time. Sphegina (S.) quadriseta is recorded for the first time in the Oriental region. A key to all the Oriental species of Sphegina is provided. The Oriental fauna of Sphegina now comprises 94 species.
The Swedish species of Enicospilus are reviewed. Three species are described from Swedish material; Enicospilus cederbergi sp. nov., Enicospilus intermedius sp. nov. and Enicospilus ryrholmi sp. nov. Four species: Enicospilus cerebrator Aubert, 1966, Enicospilus combustus (Gravenhorst, 1829), Enicospilus merdarius (Gravenhorst, 1829) and Enicospilus myricae Broad & Shaw, 2016, are reported from Sweden for the first time. An illustrated key to the Swedish species of Enicospilus is provided. Validity of the new species is supported by DNA barcoding.
The Central Asian spider genus Anemesia Pocock, 1895 is rediagnosed and revised. The genus was found to contain 14 species: ♂♀ A. andreevae sp. nov. (Uzbekistan, Tajikistan); ♂♀ A. birulai (Spassky, 1937) (Turkmenistan); ♂♀ A. castanea sp. nov.; ♂♀ A. incana Zonstein, 2001, ♂♀ A. infumata sp. nov.; ♂♀ A. infuscata sp. nov.; ♂♀ A. karatauvi (Andreeva, 1968) (all Tajikistan); ♂ A. koponeni Marusik, Zamani & Mirshamsi, 2014 (Iran); ♂♀ A. oxiana sp. nov.; ♂♀ A. pallida sp. nov.; ♂ A. parvula sp. nov. (all Tajikistan); ♂♀ A. pococki sp. nov. (Turkmenistan); ♂♀ A. sogdiana sp. nov. (Uzbekistan, Tajikistan) and ♂♀ A. tubifex (Pocock, 1889), the type species (Afghanistan, Turkmenistan). Nine species are newly described; others are redescribed from types and/or conspecific material. Males of A. tubifex and females of A. birulai, hitherto unknown, are described for the first time. Data on the variability, relationships, distribution, and ecology of all considered species are provided.
A new species of the Afrotropical genus Genaemirum Heinrich, 1936 is described from a single female specimen from Guinea and compared to the closest species, G. rhinoceros Heinrich, 1967. Genaemirum filipazzii sp. nov. also provides the first record of the genus for West Africa. An updated key to the species is included.
Three new species of Willowsia collected from Guizhou Province, China are described here: W. sexachaeta sp. nov., W. christianseni sp. nov., and W. tanae sp. nov. They have spinulate scales on the body. Colour pattern and dorsal chaetotaxy are the main diagnostic characters for these species. A table summarizing the main differences between all Chinese Willowsia species is given.
Twenty species of the genus Chilocorus Leach, 1815 currently known from China are recorded, including two new species described here: C. nigricaeruleus Li & Wang sp. nov. and C. strenotubus Li & Wang sp. nov. Diagnoses and detailed descriptions of the new species are given. Each species is illustrated in detail, including genitalia. Distribution maps, a key to the Chinese species and a world checklist of Chilocorus are given.
Although extensively studied by different authors over the past 150 years, the taxonomy of Canthon Hoffmannsegg, 1817 and allied genera (which are here informally referred to as 'Canthon sensu lato') still remains problematic. With the aim of resolving some of the questions surrounding these taxa, the present work reviews the taxonomy of one of them, the genus Sylvicanthon Halffter & Martínez, 1977. As defined here, Sylvicanthon is distributed mainly throughout the vast areas of tropical rainforests in the Neotropical region and includes 15 species divided into two groups: the enkerlini group, with a single species, S. enkerlini (Martínez et al., 1964) comb. nov., and the candezei group, with five subgroups: the candezei subgroup, with S. candezei (Harold, 1869), S. genieri sp. nov. and S. foveiventris (Schmidt, 1920); the aequinoctialis subgroup, with S. aequinoctialis (Harold, 1868) comb. nov. and S. proseni (Martínez, 1949) stat. et comb. nov.; the bridarollii subgroup, with S. bridarollii (Martínez, 1949), S. seag sp. nov., S. edmondsi sp. nov. and S. attenboroughi sp. nov.; the furvus subgroup, with S. furvus (Schmidt, 1920), S. monnei sp. nov., S. mayri sp. nov. and S. obscurus (Schmidt, 1920); and the securus subgroup, with a single species, S. securus (Schmidt, 1920) comb. nov. Three species originally included in Sylvicanthon are here (re)transferred to Canthon: Canthon xanthopus Blanchard, 1846 and C. machadoi (Martínez & Pereira, 1967) comb. nov., as well as C. cobosi (Pereira & Martínez, 1960) stat. et comb. nov., which had been previously in synonymy under C. xanthopus. Descriptions, redescriptions, illustrations and comparative tables on the external morphology (including the genital capsule) of the genus and its species are presented, as well as a detailed discussion on their biogeography, comparative morphology, hypotheses on their phylogenetic relationships, data on natural history and a detailed historical revision of the classification of 'Canthon sensu lato'. Finally, we also discuss the socalled 'species problem' (i.e., the definition of the scientific term 'species') and its consequences to dung beetle taxonomy and favour the solution offered by the Biological Species Concept.
The ‘gigas’ group of dragon millipedes, formerly placed in the genus Desmoxytes Chamberlin, 1923, is revised and assigned to the new genus Gigaxytes gen. nov. Desmoxytes gigas Golovatch & Enghoff, 1994 is the type species of the new genus and is redescribed as G. gigas (Golovatch & Enghoff, 1994) gen. et comb nov. Three new species are described: G. fusca gen et sp. nov. from Thailand and Myanmar; G. parvoterga gen et sp. nov. and G. suratensis gen et sp. nov. from Thailand. All Gigaxytes species are endemic to small distribution areas in limestone habitats in South Thailand and South Myanmar. Illustrations of external morphological characters and an identification key to all known species are provided as well as a distribution map.