Revision of the Malagasy genus Trichoteleia Kieffer (Hymenoptera, Platygastroidea, Platygastridae)

The species of the genus Trichoteleia Kieffer (Hymenoptera: Platygastridae) are revised: 42 species are recognized, of which two were previously named and are redescribed: Trichoteleia afo Talamas, sp. n., Trichoteleia albidipes Kieffer, Trichoteleia bicolor Talamas, sp. n.; Trichoteleia bidentata Talamas sp. n.; Trichoteleia carinata Talamas, sp. n.; Trichoteleia cincta Talamas & Masner, sp. n.; Trichoteleia delilah Talamas, sp. n.; Trichoteleia eburata Talamas, sp. n.; Trichoteleia echinata Talamas, sp. n.; Trichoteleia fisheri Talamas & Masner, sp. n.; Trichoteleia funesta Talamas, sp. n.; Trichoteleia halterata Talamas & Masner, sp. n.; Trichoteleia hemlyae Talamas & Masner, sp. n.; Trichoteleia irwini Talamas & Masner, sp. n.; Trichoteleia janus Talamas, sp. n.; Trichoteleia jiro Talamas, sp. n.; T. ketrona Talamas, sp. n.; Trichoteleia levii Talamas & Johnson, sp. n.; Trichoteleia longiventris Talamas & Masner, sp. n.; Trichoteleia minima Talamas, sp. n.; Trichoteleia nify Talamas & Masner, sp. n.; Trichoteleia oculea Talamas, sp. n.; Trichoteleia orona Talamas & Masner, sp. n.; Trichoteleia parvipennis Talamas & Masner, sp. n.; Trichoteleia pauliani (Risbec); Trichoteleia picturata Talamas, sp. n.; Trichoteleia prima Talamas, sp. n.; Trichoteleia prolixa Talamas, sp. n.; Trichoteleia quazii Talamas, sp. n.; Trichoteleia ravaka Talamas, sp. n.; Trichoteleia rugifrons Talamas & Masner, sp. n.; Trichoteleia solocis Talamas, sp. n.; Trichoteleia sphaerica Talamas, sp. n.; Trichoteleia subtilis Talamas & Masner, sp. n.; Trichoteleia tahotra Talamas & Masner, sp. n.; Trichoteleia takariva Talamas, sp. n.; Trichoteleia tezitra Talamas, sp. n.; Trichoteleia tigris Talamas, sp. n.; Trichoteleia tonsa Talamas, sp. n.; Trichoteleia warreni Talamas & Masner, sp. n.; Trichoteleia xantrox Talamas, sp. n.; Trichoteleia zuparkoi Talamas & Masner, sp. n. A neotype is designated for Trichoteleia albidipes and a lectotype is designated for Trichoteleia pauliani.     

Further studies on the Pselaphodes complex of genera from China (Coleoptera,Staphylinidae, Pselaphinae)

New data on the Pselaphodes complex of genera (Pselaphitae: Tyrini) from China is presented. The generic limits of Labomimus Sharp and Pselaphodes Westwood are discussed and expanded. A revised key to the genera of the Pselaphodes complex is provided. New geographic evidence suggests that previously believed wide-spread species Pselaphodes tianmuensis Yin, Li & Zhao contains a number of related species, resulting in a division of the species to nine separate taxa. Fourteen new species belonging to three genera are diagnosed, described and illustrated: Dayao emeiensis Yin & Li, sp. n. (Sichuan), Labomimus fimbriatus Yin & Hlaváč, sp. n. (Yunnan), Labomimus jizuensis Yin & Hlaváč, sp. n. (Yunnan), Labomimus simplicipalpus Yin & Hlaváč, sp. n. (Sichuan), Pselaphodes anhuianus Yin & Li, sp. n. (Anhui), Pselaphodes daii Yin & Hlaváč, sp. n. (Sichuan), Pselaphodes grebennikovi Yin & Hlaváč, sp. n. (Yunnan), Pselaphodes hainanensis Yin & Li, sp. n. (Hainan), Pselaphodes kuankuoshuiensis Yin & Li, sp. n. (Guizhou), Pselaphodes longilobus Yin & Hlaváč, sp. n. (Hunbei, Yunnan), Pselaphodes monoceros Yin & Hlaváč, sp. n. (Xizang), Pselaphodes pengi Yin & Li, sp. n. (Sichuan), Pselaphodes tiantongensis Yin & Li, sp. n. (Zhejiang) and Pselaphodes wrasei Yin & Li, sp. n. (Yunnan). Labomimus sichuanicus Hlaváč, Nomura & Zhou (Sichuan) is redescribed and illustrated based on a paratype and the material from the type locality. Two recently described species, Pselaphodes tibialis Yin & Li (Yunnan), and Pselaphodes venustus Yin & Li (Yunnan), are transferred to Labomimus (comb. n.) due to the presence of a median metaventral fovea. New locality data is provided for Pselaphodes aculeus Yin, Li & Zhao (Anhui, Fujian, Guangxi, Hainan, Yunnan), Pselaphodes maoershanus Yin & Li (Guangxi, Guizhou), Pselaphodes tianmuensis (Zhejiang, Anhui, Fujian, Jiangxi, Guangxi) and Pselaphodes pectinatus Yin, Li & Zhao (Hainan), with the aedeagus newly illustrated for the latter species.     

Systematics of Old World Odontacolus Kieffer s.l. (Hymenoptera,Platygastridae s.l.): parasitoids?of?spider?eggs

The genera Odontacolus Kieffer and Cyphacolus Priesner are among the most distinctive platygastroid wasps because of their laterally compressed metasomal horn; however, their generic status has remained unclear. We present a morphological phylogenetic analysis comprising all 38 Old World and four Neotropical Odontacolus species and 13 Cyphacolus species, which demonstrates that the latter is monophyletic but nested within a somewhat poorly resolved Odontacolus. Based on these results Cyphacolus syn. n. is placed as a junior synonym of Odontacolus which is here redefined. The taxonomy of Old World Odontacolus s.str. is revised; the previously known species Odontacolus longiceps Kieffer (Seychelles), Odontacolus markadicus Veenakumari (India), Odontacolus spinosus (Dodd) (Australia) and Odontacolus hackeri (Dodd) (Australia) are re-described, and 32 new species are described: Odontacolus africanus Valerio & Austin sp. n. (Congo, Guinea, Kenya, Madagascar, Mozambique, South Africa, Uganda, Zimbabwe), Odontacolus aldrovandii Valerio & Austin sp. n. (Nepal), Odontacolus anningae Valerio & Austin sp. n. (Cameroon), Odontacolus australiensis Valerio & Austin sp. n. (Australia), Odontacolus baeri Valerio & Austin sp. n. (Australia), Odontacolus berryae Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus bosei Valerio & Austin sp. n. (India, Malaysia, Sri Lanka), Odontacolus cardaleae Valerio & Austin sp. n. (Australia), Odontacolus darwini Valerio & Austin sp. n. (Thailand), Odontacolus dayi Valerio & Austin sp. n. (Indonesia), Odontacolus gallowayi Valerio & Austin sp. n. (Australia), Odontacolus gentingensis Valerio & Austin sp. n. (Malaysia), Odontacolus guineensis Valerio & Austin sp. n. (Guinea), Odontacolus harveyi Valerio & Austin sp. n. (Australia), Odontacolus heratyi Valerio & Austin sp. n. (Fiji), Odontacolus heydoni Valerio & Austin sp. n. (Malaysia, Thailand), Odontacolus irwini Valerio & Austin sp. n. (Fiji), Odontacolus jacksonae Valerio & Austin sp. n. (Cameroon, Guinea, Madagascar), Odontacolus kiau Valerio & Austin sp. n. (Papua New Guinea), Odontacolus lamarcki Valerio & Austin sp. n. (Thailand), Odontacolus madagascarensis Valerio & Austin sp. n. (Madagascar), Odontacolus mayri Valerio & Austin sp. n. (Indonesia, Thailand), Odontacolus mot Valerio & Austin sp. n. (India), Odontacolus noyesi Valerio & Austin sp. n. (India, Indonesia), Odontacolus pintoi Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus schlingeri Valerio & Austin sp. n. (Fiji), Odontacolus sharkeyi Valerio & Austin sp. n. (Thailand), Odontacolus veroae Valerio & Austin sp. n. (Fiji), Odontacolus wallacei Valerio & Austin sp. n. (Australia, Indonesia, Malawi, Papua New Guinea), Odontacolus whitfieldi Valerio & Austin sp. n. (China, India, Indonesia, Sulawesi, Malaysia, Thailand, Vietnam), Odontacolus zborowskii Valerio & Austin sp. n. (Australia), and Odontacolus zimi Valerio & Austin sp. n. (Madagascar). In addition, all species of Cyphacolus are here transferred to Odontacolus: Odontacolus asheri (Valerio, Masner & Austin) comb. n. (Sri Lanka), Odontacolus axfordi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus bhowaliensis (Mani & Mukerjee) comb. n. (India), Odontacolus bouceki (Austin & Iqbal) comb. n. (Australia), Odontacolus copelandi (Valerio, Masner & Austin) comb. n. (Kenya, Nigeria, Zimbabwe, Thailand), Odontacolus diazae (Valerio, Masner & Austin) comb. n. (Kenya), Odontacolus harteni (Valerio, Masner & Austin) comb. n. (Yemen, Ivory Coast, Paskistan), Odontacolus jenningsi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus leblanci (Valerio, Masner & Austin) comb. n. (Guinea), Odontacolus lucianae (Valerio, Masner & Austin) comb. n. (Ivory Coast, Madagascar, South Africa, Swaziland, Zimbabwe), Odontacolus normani (Valerio, Masner & Austin) comb. n. (India, United Arab Emirates), Odontacolus sallyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tessae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tullyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus veniprivus (Priesner) comb. n. (Egypt), and Odontacolus watshami (Valerio, Masner & Austin) comb. n. (Africa, Madagascar). Two species of Odontacolus are transferred to the genus Idris Förster: Idris longispinosus (Girault) comb. n. and Idris amoenus (Kononova) comb. n., and Odontacolus doddi Austin syn. n. is placed as a junior synonym of Odontacolus spinosus (Dodd). Odontacolus markadicus, previously only known from India, is here recorded from Brunei, Malaysia, Sri Lanka, Thailand and Vietnam. The relationships, distribution and biology of Odontacolus are discussed, and a key is provided to identify all species.     

A butterfly with olive green eyes discovered in the United States and the Neotropics (Lepidoptera,Lycaenidae, Eumaeini)

We describe Ministrymon janevicroy Glassberg, sp. n., from the United States (Texas). Its wing pattern closely resembles that of the widespread and well-known lycaenid, Ministrymon azia (Hewitson). The new species is distinguished by the structure of its male and female genitalia, by the patterning of the ground color on the basal half of the ventral hindwing surface, and by the color of its eyes. Adults of Ministrymon janevicroy in nature have olive green eyes in contrast to the dark brown/black eyes of Ministrymon azia. Ministrymon janevicroy occurs in dry deciduous forest and scrub from the United States (Texas) to Costa Rica (Guanacaste) with disjunct populations on Curaçao and Isla Margarita (Venezuela). In contrast, Ministrymon azia occurs from the United States to southern Brazil and Chile in both dry and wet lowland habitats. Nomenclaturally, we remove the name Electrostrymon grumus K. Johnson & Kroenlein, 1993, from the synonymy of Ministrymon azia (where it had been listed as a synonym of Ministrymon hernandezi Schwartz & K. Johnson, 1992). We accord priority to Angulopis hernandezi K. Johnson & Kroenlein, 1993 over Electrostrymon grumus K. Johnson & Kroenlein, 1993, syn. n., which currently is placed in Ziegleria K. Johnson, 1993. The English name Vicroy’s Ministreak is proposed for Ministrymon janevicroy. We update biological records of dispersal and caterpillar food plants, previously attributed to Ministrymon azia, in light of the new taxonomy.     

Taxonomic revision and molecular phylogeny of the fig wasp genus AnidarnesBouček, 1993 (Hymenoptera: Sycophaginae)

Besides the pollinators (Agaonidae), several chalcidoid lineages of nonpollinating fig wasps are strictly dependent on Ficus (Moraceae) for reproduction. Overall, nonpollinating fig wasps have not received much consideration. Reliable phylogenetic and taxonomic frameworks are lacking for most groups, which hampers progress in our understanding of the evolution and functioning of fig wasp communities. Here we focus on Anidarnes Bou?ek (Sycophaginae), a member of the Neotropical fig wasp community. We present a detailed morphological analysis as well as the first molecular phylogeny of the genus inferred from two nuclear and two mitochondrial genes (Cytb, COI, EF‐1α and 28S rRNA, 3937 bp). Twelve species are recognised, illustrated and a key to their identification is provided. Of those, only three were previously described and are redescribed here: A. bicolor (Ashmead); A. globiceps (Mayr) and A. brevicauda Bou?ek. In addition, nine new species are described: Anidarnes brevior sp.n . Farache & Rasplus (Costa Rica); A. dissidens sp.n. Farache & Rasplus (Brazil); A. gracilis sp.n. Farache & Rasplus (Costa Rica); A. isophlebiae sp.n. Farache & Rasplus (Costa Rica); A. jimeneziae sp.n. Farache & Rasplus (Costa Rica); A. longiscutellum sp.n. Farache & Rasplus (Brazil); A. martinae sp.n. Farache & Rasplus (U.S.A., Florida); A. nigrus sp.n. Farache & Rasplus (Colombia) and A. rugosus sp.n. Farache & Rasplus (Brazil). Finally, phylogenetic relationships inferred using parsimony, bayesian and maximum likelihood methods are discussed in the light of our morphological observations and the host fig tree taxonomy.     

On the Lathrobium fauna of the Emei Shan,Sichuan, China (Coleoptera,Staphylinidae, Paederinae)

Six species of Lathrobium Gravenhorst, 1802 from the Emei Shan, Sichuan, are described and illustrated: Lathrobium iunctum Assing & Peng sp. n., Lathrobium coniunctum Assing & Peng sp. n., Lathrobium conexum Assing & Peng sp. n., Lathrobium ensigerum Assing & Peng sp. n., Lathrobium hastatum Assing & Peng sp. n., and Lathrobium bisinuatum Assing & Peng sp. n. Based on their primary and secondary sexual characters, they represent two distinct lineages, each of them comprising three species. A key to the species recorded from the Emei Shan is provided.     

Description of three new Triaenodes species from Fiji (Trichoptera,Leptoceridae)

The following three new species are illustrated and described from Fiji: Triaenodes rebellus Eriksson & Johanson, sp. n., Triaenodes oscitus Müller & Johanson, sp. n., and Triaenodes forcipatus Puranen Li & Johanson, sp. n. All species are endemic to Viti Levu. A key to the male Triaenodes species of Fiji is provided. With this report, the number of Triaenodes species known from Fiji is doubled.     

New species and records of Lobrathium Mulsant & Rey (Coleoptera,Staphylinidae, Paederinae) from China

Seven new species of the genus Lobrathium Mulsant & Rey from China are described and illustrated: Lobrathium anatinum Li & Li, sp. n. (Guangxi), Lobrathium diaoluoense Li & Li, sp. n. (Hainan), Lobrathium dufui Li & Li, sp. n. (Hubei), Lobrathium lirunyui Li & Li, sp. n. (Guizhou), Lobrathium pengi Li & Li, sp. n. (Guangxi), Lobrathium quyuani Li & Li, sp. n. (Hubei) and Lobrathium uncinatum Li & Li, sp. n. (Qinghai). A recent key to the species of mainland China is modified to accommodate the new species. New locality data are provided for eleven species.     

Review of the species level taxonomy of the neotropical butterfly genus Oenomaus (Lycaenidae,?Theclinae,?Eumaeini)

Seven new species of the Neotropical hairstreak genus Oenomaus are described: Oenomaus mancha Busby & Faynel, sp. n. (type locality Ecuador); Oenomaus gwenish Robbins & Faynel, sp. n. (type locality Panama); Oenomaus lea Faynel & Robbins, sp. n. (type locality Ecuador); Oenomaus myrteana Busby, Robbins & Faynel, sp. n. (type locality Ecuador); Oenomaus mentirosa Faynel & Robbins, sp. n. (type locality Peru); Oenomaus andi Busby & Faynel, sp. n. (type locality Ecuador) and Oenomaus moseri Robbins & Faynel, sp. n. (type locality Brazil, Santa Catarina). For each new Oenomaus species, we present diagnostic characters and notes on its habitat and biology. We illustrate adults, genitalia, and distribution. New distributional and biological data are presented for 21 previously described Oenomaus species. Oenomaus melleus guyanensis Faynel, 2008 is treated as a new synonym of Oenomaus melleus melleus (Druce, 1907). Females are described and associated with males for ten species using a variety of factors, including mitochondrial COI DNA “barcode” sequences. We summarize the reasons why the number of recognized Oenomaus species has grown in the past decade from one species to 28 species. Finally, we overview the habitats that Oenomaus species occupy and note that the agricultural pest on Annonaceae, Oenomaus ortygnus, is the only Oenomaus species that regularly occurs in greatly disturbed habitats.     

Eight new apterous Lathrobium species (Coleoptera,Staphylinidae) from Sichuan,Southwest China

Eight apterous species of the paederine genus Lathrobium Gravenhorst, 1802 from the Chinese province Sichuan are described, illustrated, and distinguished from closely related and/or geographically close congeners: Lathrobium erlangense Peng & Li sp. n. (Erlang Shan), Lathrobium blandum Peng & Li sp. n. (Labahe N. R.), Lathrobium yelense Peng & Li sp. n. (Yele), Lathrobium obscurum Peng & Li sp. n. (Yele), Lathrobium yinziweii Peng & Li sp. n. (Yele), Lathrobium illustre Peng & Li sp. n. (Yele), Lathrobium micangense Peng & Li sp. n. (Micang Shan) and Lathrobium agglutinatum Assing & Peng sp. n. (Qingcheng Shan). The total number of described Lathrobium species from Sichuan now stands at 39, that of mainland China at 165.     

A synopsis of the tribe Lachnophorini,with a new genus of Neotropical distribution and a revision of the Neotropical genus Asklepia Liebke, 1938 (Insecta,Coleoptera, Carabidae)

This synopsis provides an identification key to the genera of Tribe Lachnophorini of the Western and Eastern Hemispheres including five genera previously misplaced in carabid classifications. The genus Asklepia Liebke, 1938 is revised with 23 new species added and four species reassigned from Eucaerus LeConte, 1853 to Asklepia Liebke, 1938. In addition, a new genus is added herein to the Tribe: Peruphorticus gen. n. with its type species P. gulliveri sp. n. from Perú. Five taxa previously assigned to other tribes have adult attributes that make them candidates for classification in the Lachnophorini: Homethes Newman, Aeolodermus Andrewes, Stenocheila Laporte de Castelnau, Diplacanthogaster Liebke, and Selina Motschulsky are now considered to belong to the Lachnophorini as genera incertae sedis. Three higher level groups are proposed to contain the 18 recognized genera: the Lachnophorina, Eucaerina, and incertae sedis.Twenty-three new species of the genus Asklepia are described and four new combinations are presented. They are listed with their type localities as follows: (geminata species group) Asklepia geminata (Bates, 1871), comb. n, Santarém, Rio Tapajós, Brazil; (hilaris species group) Asklepia campbellorum Zamorano & Erwin, sp. n., 20 km SW Manaus, Brazil, Asklepia demiti Erwin & Zamorano, sp. n., circa Rio Demiti, Brazil, Asklepia duofos Zamorano & Erwin, sp. n., 20 km SW Manaus, Brazil, Asklepia hilaris (Bates, 1871), comb. n, São Paulo de Olivença, Brazil, Asklepia grammechrysea Zamorano & Erwin, sp. n., circa Pithecia, Cocha Shinguito, Perú, Asklepia lebioides (Bates, 1871), comb. n, Santarém, Rio Tapajós, Brazil, Asklepia laetitia Zamorano & Erwin, sp. n., Leticia, Colombia, Asklepia matomena Zamorano & Erwin, sp.n., 20 km SW Manaus, Brazil; (pulchripennis species group) Asklepia adisi Erwin & Zamorano, sp. n., Ilha de Marchantaria, Lago Camaleão, Brazil, Asklepia asuncionensis Erwin & Zamorano, sp. n., Asunción, Río Paraguay, Paraguay, Asklepia biolat Erwin & Zamorano, sp. n., BIOLAT Biological Station, Pakitza, Perú, Asklepia bracheia Zamorano & Erwin, sp. n., circa Explornapo Camp, Río Napo, Cocha Shimagai, Perú, Asklepia cuiabaensis Erwin & Zamorano, sp. n., Cuiabá, Brazil, Asklepia ecuadoriana Erwin & Zamorano, sp. n., Limoncocha, Ecuador, Asklepia kathleenae Erwin & Zamorano, sp. n., Belém, Brazil, Asklepia macrops Erwin & Zamorano, sp. n., Concordia, Río Uruguay, Argentina, Asklepia marchantaria Erwin & Zamorano, sp. n., Ilha de Marchantaria, Lago Camaleão, Brazil, Asklepia marituba Zamorano & Erwin, sp. n., Marituba, Ananindeua, Brazil, Asklepia paraguayensis Zamorano & Erwin, sp. n., San Lorenzo, Rio Paraguay, Paraguay, Asklepia pakitza Erwin & Zamorano, sp. n., BIOLAT Biological Station, Pakitza, Perú, Asklepia pulchripennis (Bates, 1871), comb. n, Santarém, Rio Tapajós, Brazil, Asklepia samiriaensis Zamorano & Erwin, sp. n., Boca del Río Samiria, Perú, Asklepia stalametlitos Zamorano & Erwin, sp. n., Guayamer, Río Mamoré, Bolivia, Asklepia strandi Liebke, 1938, Guyana, Asklepia surinamensis Zamorano & Erwin, sp. n., l’Hermitage, Surinam River, Surinam, Asklepia vigilante Erwin & Zamorano, sp. n., Boca del Río Samiria, Perú. Images of adults of all 18 genera are provided.     

Description and biology of two new species of Neotropical Liriomyza Mik (Diptera,Agromyzidae), mining leaves of Bocconia (Papaveraceae)

Liriomyza mystica Boucher & Nishida, sp. n., and Liriomyza prompta Boucher & Nishida, sp. n. are described from Costa Rica. Both species were reared from leaves of Bocconia frutescens L. (Papaveraceae). The latter species was also reared from B. arborea S. Watson. Larvae of L. mystica mine primary veins of large, relatively old, mature leaves, and L. prompta mine blades of small to large, mature leaves. These represent the first record of agromyzids feeding on Bocconia. Biological information is also given and illustrated.     

The genus Macroteleia Westwood (Hymenoptera,Platygastridae s. l., Scelioninae) from China

The genus Macroteleia Westwood (Hymenoptera: Platygastridae s. l., Scelioninae) from China is revised. Seventeen species are recognized based on 502 specimens, all of which are new records for China. Seven new species are described: Macroteleia carinigena sp. n. (China), Macroteleia flava sp. n. (China), Macroteleia gracilis sp. n. (China), Macroteleia salebrosa sp. n. (China), Macroteleia semicircula sp. n. (China), Macroteleia spinitibia sp. n. (China) and Macroteleia striatipleuron sp. n. (China). Ten species are redescribed: Macroteleia boriviliensis Saraswat (China, India, Thailand), Macroteleia crawfordi Kiefer, stat. n. (China, Philippines, Thailand, Vietnam), Macroteleia dolichopa Sharma (China, India, Vietnam), Macroteleia emarginata Dodd (China, Malaysia), Macroteleia indica Saraswat & Sharma (China, India, Vietnam), Macroteleia lamba Saraswat & Sharma (China, India, Thailand, Vietnam), Macroteleia livingstoni Saraswat (China, India), Macroteleia peliades Kozlov & Lê (China, Vietnam), Macroteleia rufa Szelényi (China, Egypt, Georgia, Russia, Thailand, Ukraine) and Macroteleia striativentris Crawford (China, Philippines, Thailand, Vietnam). The following five new synonyms are proposed: Macroteleia crates Kozlov & Lê syn. n. and Macroteleia demades Kozlov & Lê syn. n. of Macroteleia crawfordi Kieffer; Macroteleia cebes Kozlov & Lê syn. n. and Macroteleia dones Kozlov & Lê syn. n. of Macroteleia indica Saraswat & Sharma; Macroteleia dores Kozlov & Lê syn. n. of Macroteleia lamba Saraswat & Sharma. A key to the Chinese species of the genus is provided.     

A New Species and New Combinations of Brevitobrilus Tsalolikhin, 1981 (Nematoda: Tobrilidae) from Spain

A new species of Brevitobrilus Tsalolikhin, Brevitobrilus montanus n. sp., found in high mountain lakes and rivers in Granada, Spain, is described. Additional data on Brevitobrilus granatensis (Ocafia &Zullini, 1988) n. comb. are provided. Brevitobrilus raontanus n. sp. is characterized by moderate size (1.3-1.8 mm), amphid aperture width one-quarter the head width, subterminal seta distance from terminus four times the width of the terminal end of the tail, and supplements S5 and S6 separated. Tobrilus granatensis Ocafia &Zullini, 1988; Tobrilus sardus Vinciguerra &Zullini, 1991; and Tobrilus siculus Vinciguerra &Zullini, 1991 are all transferred to Brevitobrilus. Differences among the 13 species of Brevitobrilus are discussed.     

Review and redescription of species in the Oecetis avara group,with the description of 15 new species (Trichoptera,Leptoceridae)

The O. avara group of Oecetis is formally defined to include 4 described species, O. avara (Banks), O. disjuncta (Banks), O. elata Denning & Sykora, and O. metlacenis Bueno-Soria, and 15 new species. Oecetis marquesi Bueno-Soria, previously considered a member of the O. avara group, is treated as incertae sedis to species group, but is also redescribed and treated in the current work. New species described here (with their respective distributions) include: O. acciptrina (Costa Rica, Panama, Ecuador), O. agosta (Mexico), O. angularis (Guatemala to Ecuador), O. apache (SW USA), O. campana (Ecuador), O. constricta (Mexico to Ecuador, Venezuela, and Trinidad), O. houghtoni (North America), O. maritza (Costa Rica), O. mexicana (Mexico to Ecuador), O. patula (Guatemala, Nicaragua), O. protrusa (Mexico to Ecuador), O. sordida (Mexico, USA, Canada), O. tumida (Costa Rica), O. uncata (Costa Rica), and O. verrucula (Mexico to Costa Rica). A key to the species is also provided.     

Nuclear ribosomal internal transcribed spacer 1 (ITS1) variation in the Anastrepha fraterculus cryptic species complex (Diptera,Tephritidae) of the Andean region

The nuclear ribosomal internal transcribed spacer 1 (ITS1) was sequenced for Anastrepha fraterculus (Wiedemann, 1830) originating from 85 collections from the northern and central Andean countries of South America including Argentina (Tucumán), Bolivia, Perú, Ecuador, Colombia, and Venezuela. The ITS1 regions of additional specimens (17 collections) from Central America (México, Guatemala, Costa Rica, and Panamá), Brazil, Caribbean Colombia, and coastal Venezuela were sequenced and together with published sequences (Paraguay) provided context for interpretation. A total of six ITS1 sequence variants were recognized in the Andean region comprising four groups. Type I predominates in the southernmost range of Anastrepha fraterculus. Type II predominates in its northernmost range. In the central and northern Andes, the geographic distributions overlap and interdigitate with a strong elevational effect. A discussion of relationships between observed ITS1 types and morphometric types is included.     

A new species of the gamasid mite genus Arctoseius Thor, 1930 (Parasitiformes,Mesostigmata, Ascidae) from Russia with a key to the multidentatus species-group

A new gamasid mite species belonging to the genus Arctoseius Thor, 1930 is described from Russia. Arctoseius koltschaki sp. n. is distributed in the plain and mountain tundras from Khibiny Mountains to Chukotka on the north and to West Sayan Mountains on the south. A diagnosis and a key for identification of species comprising the multidentatus species-group (Arctoseius multidentatus Evans, 1955; Arctoseius wisniewskii Gwiazdowicz & Kamczyc, 2009; Arctoseius sexsetus Lindquist & Makarova, 2011; Arctoseius haarlovi Lindquist & Makarova, 2011; and Arctoseius koltschaki sp. n.) are given.