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The genera Colpixys and Xiphentedon are revised. Both genera are of Afrotropical distribution and are very similar to Entedon, but distinguished by a median strip or furrow on the propodeum replacing the median carina of Entedon. The genus Xiphentedon is characterized by the complete lateral propodeal sulci delimiting convex submedian areas, prosternum with a flange, axillula with indentate projection, and densely hairy central mesopectus. The subgenus Cederholmia Gumovsky, 1997 of Entedon is considered a junior synonym of Xiphentedon, so two of its species are moved to the genus as X. halli (Gumovsky, 1997) comb. nov. and X. danielssoni (Gumovsky, 1997) comb. nov. The genus Colpixys is characterized by the lack of characters of Xiphentedon, but also by the broadly sculptured propodeum with the deep median furrow delimited laterally by two sinuous margins. Three (one new) species are recognized in Colpixys and sixteen (thirteen new) species allocated to three groups (kayovei, danielssoni and forceps), are assigned to Xiphentedon. The new species are: Colpixys eburnus sp. nov. from Ivory Coast and the Republic of South Africa (RSA), Xiphentedon neserorum sp. nov. from RSA, X. simoni sp. nov. from Tanzania, X. dewittei sp. nov. and X. musimba sp. nov. from the Democratic Republic of the Congo (DRC), X. jeanyvesi sp. nov. from Tanzania, the Central African Republic (CAR) and RSA, X. wieringai sp. nov. from Gabon and Ivory Coast, X. kivuensis sp. nov. from DRC, X. palabora sp. nov. from RSA, X. sangha sp. nov. from CAR, X. nimba sp. nov. from Guinea, X. forceps sp. nov. from Ivory Coast, Benin and RSA, X. gerardi sp. nov. from Benin, DRC and RSA, and X. acutigena sp. nov. from Ivory Coast, DRC, Tanzania and RSA. Morphological peculiarities and possible relationships of Colpixys, Xiphentedon, Entedon and some other genera, are discussed.
The genus Seticornuta Morley, 1913 currently comprises nine described species; here, nine new species are described: S. anchanchu sp. nov., S. carinata sp. nov., S. cuckoo sp. nov., S. curupira sp. nov., S. flava sp. nov., S. muqui sp. nov., S. nigroflava sp. nov., S. quilmes sp. nov., and S. rufa sp. nov. The genus is redescribed to encompass the features found in Neotropical species and distinctions between the species in the New World and Old World are presented. The genus is recorded for the first time for Argentina, Bolivia, Ecuador, Guatemala and Peru.
Sapodilla (Manilkara zapota (L.) van Royen) is originally from the Neotropics, and has become one of the most important tropical crops in the last few decades. The major producers include India, Mexico, Sri Lanka, the Philippines, Venezuela and Guatemala. It is also a minor crop in the United States, specifically South Florida. In 2015, it was reported that Florida growers suffered a loss of up to 80% of their production due to lepidopteran pests. We surveyed two sapodilla orchards weekly in South Florida for about six months. We collected 1,070 lepidopteran individuals (i.e., larvae, pupae and adults) belonging to seven families, nine genera and ten species. Phidotricha erigens Ragonot (30%), Banisia argutula Whalley (22%) and Holcocera crassicornella Dietz (13%) were the most frequently collected species. The most abundant months were April, May and June. Florida has records for ten of the sixteen species of lepidopterans associated with sapodilla in the Americas, four of which are newly reported host records. We also recorded one new record on loquat (Eriobotrya japonica (Thunb.) Lindl.) and another new record on ficus (Ficus sp.). Finally, we found a negative relationship between climate variables and the abundance of Lepidoptera species.
We recognize and review 40 species of Chlamydastis Meyrick, 1916 (Lepidoptera: Depressariidae) from Costa Rica, including four previously described (i.e., C. vividella (Busck, 1914), revived status; C. phytoptera (Busck, 1914); C. orion Busck, 1920; and C. ungulifera (Meyrick, 1929)) and 36 new species: C. abelulatei Phillips and Brown, new species; C. carolinagodoyae Phillips and Brown, new species; C. angelsolisi Phillips and Brown, new species; C. lindapitkinae Phillips and Brown, new species; C. iangauldi Phillips and Brown, new species; C. anniapicadoae Phillips and Brown, new species; C. antonioazofeifai Phillips and Brown, new species; C. mignondavisae Phillips and Brown, new species; C. marianofigueresi Phillips and Brown, new species; C. colleenhitchcockae Phillips and Brown, new species; C. bernardoespinozai Phillips and Brown, new species; C. bobandersoni Phillips and Brown, new species; C. carlosviquezi Phillips and Brown, new species; C. christerhanssoni Phillips and Brown, new species; C. christhompsoni Phillips and Brown, new species; C. paulhansoni Phillips and Brown, new species; C. elenaulateae Phillips and Brown, new species; C. gladysrojasae Phillips and Brown, new species; C. powelli Phillips and Brown, new species; C. gracewoodae Phillips and Brown, new species; C. juanmatai Phillips and Brown, new species; C. isidrochaconi Phillips and Brown, new species; C. jimlewisi Phillips and Brown, new species; C. jimmilleri Phillips and Brown, new species; C. montywoodi Phillips and Brown, new species; C. johnnoyesi Phillips and Brown, new species; C. luisdiegogomezi Phillips and Brown, new species; C. paulthiaucourti Phillips and Brown, new species; C. dondavisi Phillips and Brown, new species; C. irenecanasae Phillips and Brown, new species; C. manuelzumbadoi Phillips and Brown, new species; C. noramartinae Phillips and Brown, new species; C. vitorbeckeri Phillips and Brown, new species; C. ronaldzunigai Phillips and Brown, new species; C. munifigueresae Phillips and Brown, new species; and C. willsflowersi Phillips and Brown, new species.COI nucleotide sequences (“DNA barcodes”) were obtained for 33 of the species, which helped associate males with females for sexually dimorphic species and revealed a few cryptic, presumably evolutionary siblings. We illustrate adults of all species, along with their male and female genitalia, where available.Nineteen species were reared from caterpillars, and their foodplants are listed. In Costa Rica, 15 species of Chlamydastis are recorded exclusively from Sapotaceae; one species each exclusively from Clethraceae, Vochysiaceae, Combretaceae, and Melastomataceae. Larvae are illustrated for 10 of the 36 new species, and superficial larval descriptions are provided based on photographs and notes. Of the 40 species of Chlamydastis reported from Costa Rica, 32 have been light-collected or reared from Área de Conservación Guanacaste.
Pholetesor acrocercophagus sp. nov., P. camerariae sp. nov. and P. indicus sp. nov.(Hymenoptera: Braconidae: Microgastrinae) are described as new to science. These three species were reared from Acrocercops sp., Acrocercops phaeospora Meyrick, 1916 and Cameraria virgulata Meyrick, 1914 (Lepidoptera: Gracillariidae), respectively. Characteristics of these new species and their affinities with related taxa are discussed. Data on habitat, host records and host plant species for all the parasitoid species is provided. A key to the Indian species of the genus Pholetesor Mason, 1981 reared from lepidopteran leafminers is also given.
The Iranian species of the genus Anomalon Panzer, 1804 (Hymenoptera: Ichneumonidae: Anomaloninae) are reviewed. Four species, Anomalon amseli (Hedwig, 1961), A. chinense (Kokujev, 1915), A. cruentatum (Geoffroy, 1785) and A. narinae Zardouei & Rakhshani sp. nov., are found to occur in Iran. The female of A. amseli is described for the first time. Anomalon chinense is a new record for Iran. A key to the known Anomalon species of Iran is provided.
The taxonomic limits of Palpostilpnus Aubert, 1961 are reviewed. The genus is characterized mainly by having a very elongated maxillary palp; head short and depressed, with mandible small and with distinct basal groove; ovipositor short and slender, needle-like. A total of seventeen species are recognized, of which ten are described as new: P. aki sp. nov., P. angka sp. nov., P. angkor sp. nov., P. hainanensis sp. nov., P. mangrovi sp. nov., P. pterodactylus sp. nov., P. ranui sp. nov., P. singaporensis sp. nov., P. tamasek sp. nov. and P. trifolium sp. nov. The combination Palpostilpnus rufinator (Aubert, 1961) stat. rev. is proposed. An illustrated key to the known species of the genus is provided.
The Afrotropical (including Malagasy Subregion) species of the genus Asobara Foerster, 1863, are revised. In addition to the redescribed 15 known species, 25 new species are described and illustrated, viz., Asobara abyssiniensis Peris-Felipo, sp. nov., A. caboverdensis van Achterberg, sp. nov., A. carinata Peris-Felipo, sp. nov., A. cracentis van Achterberg, sp. nov., A. elongitarsis van Achterberg, sp. nov., A. fletcheri Peris-Felipo, sp. nov., A. harrinsmithensis Peris-Felipo, sp. nov., A. kawandensis Peris-Felipo, sp. nov., A. kibalensis van Achterberg, sp. nov., A. laticlypeata van Achterberg, sp. nov., A. mediana van Achterberg, sp. nov., A. mellicephalata van Achterberg, sp. nov., A. natalensis Peris-Felipo, sp. nov., A. notleyi Peris-Felipo, sp. nov., A. robusta van Achterberg, sp. nov., A. sarae Peris-Felipo, sp. nov., A. somersetensis Peris-Felipo, sp. nov., A. stubbsi Peris-Felipo, sp. nov., A. taylori Peris-Felipo, sp. nov., A. vanalpheni van Achterberg, sp. nov., A. vanharteni van Achterberg, sp. nov., A. victoriana Peris-Felipo, sp. nov., A. zaprionae van Achterberg, sp. nov., A. zimbabwana Peris-Felipo, sp. nov., A. zululana Peris-Felipo, sp. nov. Moreover, the following new combination is suggested: Asobara pulchricornis (Szépligeti, 1911) comb. nov. A key to all Afrotropical (including Malagasy) species is provided for the first time.
In this study, a total of 108 Aphidiinae species, belonging to 18 genera, associated with 240 aphid species in 16 countries of the Middle East and North Africa are reviewed. 743 host aphidparasitoid associations are listed. New material was collected from various regions of Saudi Arabia during 2011–2013. Three species including Aphidius avenae Haliday, 1834, Aphidius platensis Brèthes, 1913 and Praon barbatum Mackauer, 1967 are first recorded for the fauna of this country. Lysiphlebus marismortui Mescheloff & Rosen, 1990 syn. nov. is classified as the junior synonym of Lysiphlebus confusus Tremblay & Eady, 1978. An illustrated up-to-date key to all known species of Aphidiinae that occur in the Middle East and North Africa is provided. The findings are discussed in relation to the overall parasitoid-aphid associations in the target investigated region.
Afrocampe gen. nov. is described for its only species, A. prinslooi gen. et sp. nov., from Eastern and Western Cape, South Africa. This new genus is recognized as a member of the subfamily Tetracampinae Förster, 1856 of Tetracampidae Förster, 1856 based on the possession of 5-segmented tarsi in females and 4-segmented tarsi in males, the short straight calcar, the mesoscutum with distinct notauli, the mesoscutellum with two pairs of setae, the reduced mesopleural suture and the short stigmal and long postmarginal veins of the fore wing. Afrocampe gen. nov. is characterized by a large mesosoma, a non-convex first gastral tergite, an evenly acute calcar, a 5-segmented antennal funicle, a head lacking occipital carina and facial grooves and a long fore wing with distinctly delimited speculum, a bare admarginal area with a distinct admarginal row of setae on the underside and with 3 setal tracks (hair rows) radiating from the apex of the stigmal vein. The combination of these characters suggests a special status of the new genus within the subfamily Tetracampinae. Moreover, Afrocampe gen. nov. bears some resemblance to the Australian tetracampine genus Niticampe Bouček, 1988. The position of the latter in Tetracampinae, as well as habitus features of the former, are discussed.