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New species and records of Sericini from the Indian subcontinent (Coleoptera, Scarabaeidae) II
(2019)
The current paper presents new locality records, including first state records for Mizoram and Nagaland, of 50 species of Sericini (Coleoptera: Scarabaeidae: Melolonthinae) from the Indian subcontinent. Nine new species are described herein: Maladera naveeni sp. nov., M. sujitrae sp. nov., M. thirthahalliensis sp. nov., M. viraktamathi sp. nov., Neoserica (s. lat.) reuteri sp. nov., Oxyserica goertzae sp. nov., Selaserica hosanagarana sp. nov., Serica (s. str.) eberlei sp. nov. and S. (s. str.) tashigaonensis sp. nov.
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.
The ‘acantherpestes’ group of dragon millipedes, formerly placed in the genus Desmoxytes Chamberlin, 1923, is revised and assigned to the new genus Nagaxytes Srisonchai, Enghoff & Panha gen. nov. Desmoxytes acantherpestes Golovatch & Enghoff, 1994 is the type species of the new genus and is redescribed as N. acantherpestes (Golovatch & Enghoff, 1994) gen. et comb. nov. Three new species are described from Thailand: N. erecta Srisonchai, Enghoff & Panha gen. et sp. nov. and N. gracilis Srisonchai, Enghoff & Panha gen. et sp. nov. from Kanchanaburi Province, and N. spatula Srisonchai, Enghoff & Panha gen. et sp. nov. from Tak Province. All new species are endemic to western Thailand and all are restricted to limestone habitats. Complete illustrations of external morphological characters, an identification key, and a distribution map are provided.
First records of Elachistinae are given from Thailand. Ten species of Elachistinae are reported, eight of which are described as new: Urodeta longa Sruoga & Kaila sp. nov., Elachista buszkoi Sruoga & Kaila sp. nov., E. oryx Sruoga & Kaila sp. nov., E. pellineni Sruoga & Kaila sp. nov., E. capricornis Sruoga & Kaila sp. nov., E. phichaiensis Sruoga & Kaila sp. nov., E. loeiensis Sruoga & Kaila sp. nov. and E. siamensis Sruoga & Kaila sp. nov. The new species are diagnosed and illustrated with photographs of the adults and genitalia. One species remains unidentified to species level.
A revision of the genus Acentroptera Guérin-Méneville, 1844 (Coleoptera: Chrysomelidae: Cassidinae)
(2014)
The species of the genus Acentroptera Guérin-Méneville, 1844 are revised. Thirteen species are treated as valid and are illustrated. A neotype is designated for A. tessellata Baly. Acentroptera maculata Pic from Brazil and A. rubronotata Pic from Brazil are treated as incertae sedis. Acentroptera bita n. sp. and A. lineata n. sp. both from Panama are described as new. A key to the 13 treated species is presented. Five species appear to be associated with bromeliads (Bromeliaceae).
The New World euparine scarab genera Parataenius Balthasar, 1961 and Pseudataenius Brown, 1927 are revised. Ataenius brunneus Schmidt is transferred to the genus Parataenius becoming Parataenius brunneus (Schmidt), new combination. The monospecific genus Ataenioides Petrovitz, 1973, is synonymized with Pseudataenius Brown, 1927, (new synonymy) and the type species, Ataenioides gracilitarsis Petrovitz, is given the new combination Pseudataenius gracilitarsis (Petrovitz). New species of Parataenius are described from southern South America: Parataenius selvae, P. estero, and P. martinezi. Keys for species of both genera are presented and pertinent morphological details are illustrated.
In this study, I describe two new species of Macrobiotus based on morphological data collected through light and scanning electron microscopy. Both species are accompanied by DNA sequences from four commonly used molecular markers (18S rDNA, 28S rDNA, ITS-2, and COI). Macrobiotus ovovittatus sp. nov. was discovered in Greenland and can be distinguished from similar taxa of Macrobiotus by its continuous, solid, and clearly wrinkled egg surface, adorned with sparse, very small and irregularly spaced pores. Additionally, the terminal discs of egg processes are covered in multiple light-refracting dots, resembling crocheted napkins. Macrobiotus mileri sp. nov. was found in Israel and is characterized by unique pore arrangements in its body cuticle, expressed in two distinct animal forms: (i) forma porata with large pores arranged in five distinct patches and (ii) forma aporata with single, almost undetectable pores. It also features weakly defined convex terminal discs with smooth edges. Furthermore, the phylogenetic analyses conducted in this study offer the most updated phylogeny of superclade I within the family Macrobiotidae. This facilitates additional discussion concerning the interrelationships among species within the genus Macrobiotus and the circumscription of species groups within it.
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 first Oriental species of the genus Trichopsomyia Williston, 1888, Trichopsomyia pilosa sp. nov. (Java), has been discovered and is now described. This Oriental species of Trichopsomyia has several characters strongly differing from the other species within this genus. It is hypothesized that it forms a separate group within Trichopsomyia. One species, Trichopsomyia formiciphila Downes, Skevington & Thompson, 2017, from Australia, is similar to the Oriental species described here, and the group is named after this first described species, hence the formiciphila group. The characters for a future phylogenetic analysis are discussed. The character states of the pilosity of the katepisternum and the shape of the metasternum hitherto used in a phylogenetic analysis of Syrphidae Latreille, 1802 are discussed too.