Mcleanpreston0617

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). 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.We studied wing pattern characters to distinguish closely related sympatric species Papilio zelicaon Lucas, 1852 and Papilio polyxenes Fabricius, 1775 in Southern California, and developed a morphometric method based on the ventral black postmedian band. Application of this method to the holotype of Papilio [Zolicaon variety] Coloro W. G. Wright, 1905, the name currently applied to the P. polyxenes populations, revealed that it is a P. zelicaon specimen. The name for western US polyxenes subspecies thus becomes Papilio polyxenes rudkini (F. R. Chermock, 1981), reinstated status, and we place coloro as a junior subjective synonym of P. zelicaon. Furthermore, we sequenced mitochondrial DNA COI barcodes of rudkini and coloro holotypes and compared them with those of polyxenes and zelicaon specimens, confirming rudkini as polyxenes and coloro as zelicaon.A new species of Lumbrineridae, Helmutneris vadum n. sp., is described from shallow waters near Lizard Island, Great Barrier Reef, Queensland, Australia. The new species differs from two other known species of Helmutneris by having bidentate maxillae III and no ventral limbate chaetae. Sequences of the fragments of COI and 16S rDNA for two specimens including the holotype are deposited in GenBank. A key for three species of Helmutneris known to date is provided.Two new species, Apsidophora bala sp. Necrosulfonamide in vivo nov. and Apsidophora chandrapatyae sp. nov., are described. Illustrations of adult and genitalia are provided. We also present a photograph of living specimen of A. chandrapatyae sp. nov. in natural resting posture. The two new taxa increase the number of described Apsidophora species to 3.The fossil ship-timber beetle, Adamas hukawngensis gen. et sp.n., is described and defined based on one well preserved specimen in mid-Cretaceous amber from the Hukawng Valley in Northern Myanmar. The new species can be readily distinguished from all other extinct and recent members of the family due to the presence of a lozenge-shaped scutellum with a meso-longitudinal groove. Modifications of lymexylid metathoracic wing venation and palaeobiomigratory significance are briefly discussed.Ammophila kowalczyki sp. nov. (Hymenoptera Sphecidae), a new species from Iran, is described and illustrated. In addition, new data on the distribution of six other species of Ammophila are given, among them Ammophila insignis F. Smith, 1856 from the United Arab Emirates, Ammophila laevicollis Ed. André, 1886 and Ammophila terminata F. Smith, 1856 from Spain. Of the other three, Ammophila sarekandana Balthasar, 1957 and Ammophila rauschi Dollfuss, 2013 are reported for the first time from Tajikistan, and Ammophila formosensis Tsuneki, 1971 is reported from Tajikistan and Kyrgyzstan.