Brittterp8339

The ovipositor structure of the female confirms placement of Tardrabassus in Iassinae. The female pregenital sternite and ovipositor of Hamulotettix ungulatus Dai Zhang are also illustrated for the first time. A new synonymy is also proposed Ujna consors Distant, 1908 equals Mileewa puerana Yang Meng, 2010, n. syn.Records of 81 Psychodidae (Sycoracinae 4 spp., Psychodinae 76 spp.) species/subspecies are presented in this paper based on specimens collected in Bulgaria. 46 species are new records for Bulgaria (Sycoracinae 3 spp., Psychodinae 43 spp.). The Psychodidae fauna of Bulgaria now comprises 99 species (Phlebotominae 5 spp., Sycoracinae 5 spp., Trichomyiinae 1 sp., and Psychodinae 88 spp.).In a recent article, Chandramouli et al. (2020) re-assessed the systematic position of the hylaranine frog Indosylvirana nicobariensis and proposed a new monotypic genus, Bijurana, for this species. The authors re-examined the type series of specimens and attempted to justify the recognition of a new genus using morphological and phylogenetic data. They concluded that the taxon's unique phylogenetic position, high genetic divergence (uncorrected p-distance ≥ 13.64% of the 16S rRNA mitochondrial gene), and a unique combination of morphological characters warranted the erection of the new genus.Three new species of Clavigeritae from subsaharan Africa, Zuluclavodes mulanjensis sp. nov., Zuluclavodes minor sp. nov. from southern Malawi and Articerodes jaloszynskii sp. nov. from South Africa, KwaZulu-Natal are described. Diagnosis is provided for both genera, and a key to species is given for the genus Zuluclavodes Hlaváč, 2007. Ischyroceros mirus Reichensperger, 1915 is firstly recorded from Malawi, the illustration of its aedeagus is given. All described species are illustrated and their photos are presented.The genus Cymophorus Kirby, 1827 in Asia is represented by the single species C. pulchellus Arrow, 1910. This rare species is traditionally divided into two subspecies, the nominate subspecies from India and C. pulchellus tonkinensis Schein, 1954 from Indochina. While recently, the latter was informally treated as a synonym of C. pulchellus. By examining type material and additional specimens, the differences in the external features between the individuals from the two regions are reconsidered, and the two taxa are probably not identical. Precise localities of C. pulchellus tonkinensis in China are given, and geographic distribution of both subspecies is summarized in a map.An identification key to the seven known Iranian species of the genus Coenosia Meigen, 1826 is given, including Coenosia persica Pont Parchami-Araghi, sp. nov. as well as the newly recorded C. humilis Meigen, 1826, C. nigridigita Rondani, 1866 and C. testacea (Robineau-Desvoidy, 1830). Photographs of the habitus and male genitalia of the studied material in addition to illustrations of the male genitalia of the new species are provided.Two new oribatid mite species viz. Papillacarus (Vepracarus) acaciensis sp. nov. and Licneremaeus indicus sp. nov. belonging to the respective oribatid families, Lohmanniidae and Licneremaeidae are described and illustrated. Specimens of both species were collected from litter of Acacia auriculiformis Benth. (Leguminosae) growing in different localities of the Calicut University Campus, Malappuram Dt. of Kerala. The family Licneremaeidae is recorded for the first time from India. Identification keys to all known species of the nominative subgenus Vepracarus and the genus Licneremaeus are also provided.The mimallonid genus Roelofa is revised. It is the only genus belonging to the recently erected subfamily, Roelofinae.Both sexes and genitalia are figured for all previously described species in the genus, and all are redescribed. The species Roelofa maera stat. rev. is no longer considered a synonym of R. narga based on morphological differences. We describe a new species from Guatemala R. monzoni St Laurent, Herbin Kawahara, sp. n. which is most similar to the widespread Central American R. hegewischi.The life cycle of calanoid copepods consists of eggs hatching into nauplii (6 stages) which then moult into copepodids (5 stages), followed by the final moult into the adult female and male. The family Diaptomidae contains two subfamilies, Diaptominae and Paradiaptominae, with paradiaptomids almost exclusively consisting of African taxa. The copepodid stages III, IV and V were described for some freshwater diaptomine genera (i.e., Eudiaptomus Kiefer, 1932, Aglaodiaptomus Light, 1938, Skistodiaptomus Light, 1939, Leptodiaptomus Light, 1938, Megadiaptomus Kiefer, 1936 and Diaptomus Westwood, 1836). Triptolide Copepods collected from Turfloop Dam, South Africa, with a plankton net were fixed and preserved in 70% ethanol. Calanoid copepods were studied under stereo- and light microscopes, using the wooden slide technique and features drawn. Examined specimens were identified as the copepodid stages of two African species, Lovenula falcifera (Lovén, 1845) and Metadiaptomus colonialis (van Douwe, 1914). Copepodids of the two species can be distinguished by their body size and the structure and size of the maxillipeds. The description and illustrations of three postnaupliar stages (CoIII, CoIV and CoV) are provided for both species. The identification of different stages is based on the number of urosomites, antennule development, the segmentation of legs 1-4, and the development of the fifth leg. These copepodids are compared with those of other described diaptomid genera.This revision of the Nearctic predaceous midges in the Bezzia (Bezzia) pulverea complex (Diptera Ceratopogonidae) recognizes 11 species, seven of which are new species Bezzia (B.) amblystyla, n. sp., from Maryland and Florida; B. (B.) brunneipedia, n. sp., from Florida; B. (B.) folkersti n. sp., from Florida; B. (B.) huberti, n. sp., from Maryland, Florida, Arkansas and Louisiana; B. (B.) leptostyla, n. sp., from Florida; B. (B.) marylandensis, n. sp., from Maryland; and, B. (B.) titanochela, n. sp., from Texas, Alabama and Florida. Photomicrographs of diagnostic characters of both sexes are included, and a key is provided to adult males and females of species in the Bezzia (B.) pulverea complex. Bezzia (B.) imbifida Dow Turner is transferred from the B. pulverea complex to the Bezzia (B.) expolita complex.