A Taxonomic Revision of Illiberis Walker (Lepidoptera: Zygaenidae: Procridinae) in Korea

The Korean species of Illiberis Walker are revised. A total of 10 species are recognized, including four species new to Korea: I. rotundata Jordan, I. psychina (OberthÜr), I. consimilis Leech, and I. hyalina (Staudinger). The identities of I. cybele Leech and I. assimilis Jordan, the two ambiguously defined Korean species, are reconfirmed with the examination of type specimens and additional materials. Photos of the adults and type materials are provided, and male and female genitalia of each species are illustrated. Biology and distribution for each species are briefly discussed with the larval host records from Korea.     

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.     

Phylogeny and classification of the Xeromelissinae (Hymenoptera: Apoidea, Colletidae) with special emphasis on the genus Chilicola

Abstract A phylogenetic analysis and classification are provided for the bee subfamily Xeromelissinae based on 248 morphological characters, many of which are novel and illustrated. A total of 47 ingroup species was included in the analysis, representing at least two divergent members from each described genus or subgenus and seven taxa which did not readily fall within previously described subgenera. Three most parsimonious trees were found (length, 1508; consistency index, 40; retention index, 70). The result shows that Xeromelissa renders Chilimelissa paraphyletic, and the 20 known Chilimelissa species are reassigned to Xeromelissa, giving the following new combinations: X. luisa (Toro & Moldenke) (this is the type species of Chilimelissa), X. mucar (Toro & Moldenke), X. xanthorhina (Toro), X. brevimalaris (Toro), X. rosie (Toro and Packer), X. laureli (Toro and Packer), X. chusmiza (Toro), X. longipalpa (Toro), X. pedroi (Toro & Moldenke), X. australis (Toro & Moldenke), X. chillan (Toro & Moldenke), X. farellones (Toro & Moldenke), X. machi (Toro), X. minuta (Toro & Moldenke), X. nortina (Toro & Moldenke), X. sielfeldi (Toro & Moldenke), X. obscura (Toro & Moldenke), X. irwini (Toro & Moldenke), X. nolanai (Toro & Moldenke) and X. rozeni (Toro & Moldenke). Group support was estimated using symmetric resampling and group supported/contradicted (GC) ratios, which compare the frequency of each most parsimoniously resolved clade with the alternative arrangement that was most commonly found in resampling. Relationships among subgenera for Chilicola are weakly supported. By contrast, when three previously synonymized subgenera (Stenoediscelis, Heteroediscelis and Oediscelisca) are resurrected, there is good support for all subgenera (GC ≥ 99), except two: a paraphyletic Oediscelis and a polyphyletic Anoediscelis. Both of these subgenera became monophyletic following successive approximations character weighting. Four distinctive new subgenera are described: Unicarinicola Packer subgen.n. , Obesicola Packer subgen.n. , Capitatiscopa Packer subgen.n. and Toroediscelis Packer subgen.n. , and a revised key to the subgenera of Chilicola is provided.     

Cladistic analysis and taxonomic revision of the genus Karos Goodnight & Goodnight, 1944 (Opiliones,Laniatores, Stygnopsidae)

A cladistic analysis of the genus Karos Goodnight & Goodnight, 1944, was performed using morphological data of the somatic and male genitalia characters. The analysis included 23 terminal taxa, including nine of the 11 described species of the genus plus nine new species according to the previous generic diagnosis and five species as outgroups. According to the topologies obtained by parsimony analyses, the genus is a paraphyletic assemblage, referred here as the Karos genus‐group. Therefore, the genus Karos is rediagnosed here and now includes seven species: Karos barbarikos Goodnight & Goodnight, 1944 (type), Karos parvus Goodnight & Goodnight, 1971, Karos projectus Goodnight & Goodnight, 1971, K aros hexasetosus sp. nov. , K aros monjarazi sp. nov. , K aros singularis sp. nov. , and K aros tersum sp. nov. The genera Monterella Goodnight & Goodnight, 1944, Montabunus Goodnight & Goodnight, 1945, Chapulobunus Goodnight & Goodnight, 1946, and Potosa Goodnight & Goodnight, 1947 are revalidated, rediagnosed, their respective type species are redescribed and the following species are described: Chapulobunus poblano sp. nov. and Potosa reddelli sp. nov. The genera Crettaros gen. nov. , Huasteca gen. nov. , and Mictlana gen. nov. , and the following species are described: Crettaros santibanezi sp. nov. (type), Crettaros valdezi sp. nov. , and Huasteca silhavyi sp. nov. The following new combinations are proposed: Huasteca gratiosa (Goodnight & Goodnight, 1971) comb. nov. (type), Huasteca rugosa (Goodnight & Goodnight, 1971) comb. nov. and Mictlana inops (Goodnight & Goodnight, 1971) comb. nov. (type). Karos brignolii ?ilhavý, 1974, is considered a junior synonym of Huasteca rugosa. Finally, ‘Karos’ depressus Goodnight & Goodnight, 1971 is considered incertae sedis until adult males can be studied. Diagnoses of the Karos and Paramitraceras genus‐groups, and an identification key to the eight genera and 19 species of the former are provided. © 2015 The Linnean Society of London     

A chemically defined medium for rearing Epiphyas postvittana (Lepidoptera: Tortricidae)

Abstract

The endemic New Zealand genus Neolimnia is redescribed, and a key is given to the 14 species now included. Four new species are described - Neolimnia raiti, N. pepekeiti, N. ura, and N. repo. Two new synonymies are proposed; N. ocellata Tonnoir &; Malloch with N. castanea (Hutton); and N. dubiosa Tonnoir &; Malloch with N. irrorata Tonnoir &; Malloch. Lectotypes are designated for N. tranquilla (Hutton), N. castanea (Hutton), N. obscura (Hutton), and N. striata (Hutton). Male postabdomens of all species are illustrated. Character variation and generic, subgeneric, and species relationships are discussed briefly.     

The cladistics and biology of the Callajoppa genus-group (Hymenoptera: Ichneumonidae, Ichneumoninae)

A cladistic analysis is presented for the genera of the former ichneumonine tribe Trogini. The tribe Heresiarchini is paraphyletic with respect to the Trogini, and so maintaining Trogini as a separate tribe is unsatisfactory. Within Heresiarchini, the following changes are made: (a) the subtribes Apatetorina and Heresiarchina are referred to as the Apatetor and Heresiarches genus‐groups, (b) the genera of the paraphyletic subtribe Protichneumonina are treated as incerta sedis within Heresiarchini, and (c) the Trogini are referred to as the Callajoppa genus‐group, with the former subtribe Trogina referred to as the Trogus subgroup. Thirty‐five genera are recognized as valid within the Callajoppa genus‐group. Catadelphops, Catadelphus, Cobunus, and Facydes are transferred to this group; Holojoppa is removed and is incertae sedis within Heresiarchini. Three new synonyms are proposed: Araeoscelis and Cryptopyge are junior synonyms of Macrojoppa, and Neamblyjoppa is a junior synonym of Catadelphops. Trogus latipennis Cresson is transferred to Pedinopelte from Macrojoppa, and Trogus mactator Tosquinet and its related species (T. bicolor Radoszkowski, T. heinrichi Uchida, and T. tricephalus Uchida) are transferred to Holcojoppa. Tricyphus is redefined and a neotype is designated for Tricyphus cuspidiger Kriechbaumer, the type‐species of the genus. Thirteen new genera are described (authorship of all is Wahl & Sime): Charmedia (type‐species: Charmedia chavarriai Wahl & Sime, sp. n.) , Daggoo (type‐species: Daggoo philoctetes Wahl & Sime, sp. n.), Dothenia (type‐species: Dothenia hansoni Wahl & Sime, sp. n.), Humbert (type‐species: Humbert humberti Wahl & Sime, sp. n.), Laderrica (type‐species: Laderrica feenyi Wahl & Sime, sp. n.), Mokajoppa (type‐species: Tricyphus respinozai Ward & Gauld), Metallichneumon (type‐species: Metallichneumon neurospastarchus Wahl & Sime, sp. n.), Myocious (type‐species: Myocious orientalis Wahl & Sime, sp. n.) , Quandrus (type‐species: Trogus pepsoides Smith, transferred from Callajoppa), Queequeg (type‐species: Gathetus flavibasalis Uchida, transferred from Neofacydes), Saranaca (type‐species: Trogus elegans Cresson; includes Trogus apicalis Cresson, Tricyphyus ater Hopper, and Tricyphus floridanus Heinrich), Tashtego (type‐species: Tashtego janzeni Wahl & Sime, sp. n.), and Xanthosomnium (type‐species: Xanthosomnium froesei Wahl & Sime, sp. n.). A key to the genera of the Callajoppa genus‐group is provided. The evolution of biological traits within the Callajoppa genus‐group is discussed with reference to the elucidated phylogeny. The groundplan biology is parasitism of Sphingidae, with oviposition into a host pupa/prepupa. There have been two transitions to butterfly parasitism within the Trogus subgroup: one a transition to Papilionidae (followed by a switch to Nymphalidae at Psilomastax) and the other to Nymphalidae (followed by a switch to Papilionidae within Macrojoppa). ©2002 The Linnean Society of London. Zoological Journal of the Linnean Society, 134 , 1–56.     

The Old World species of Pouzolzia (Urticaceae, tribus Boehmerieae). A taxonomic revision

The Old World species of the genus Pouzolzia have been revised and 24 species and 13 infraspecific taxa recognised. Worldwide, the genus now totals 36 species and 17 infraspecific taxa. Pouzolzia sect. Memorialis Bennett & Brown (including the genera Gonostegia Turcz. and Hyrtanandra Miq.) is maintained here as a section of Pouzolzia. The characters used to separate Pouzolzia from Boehmeria are found to work worldwide. In the Old World, the genus ranges, west to east, from Senegal to Japan and the Solomon Islands, and, north to south, from China, the Himalayas and Yemen to South Africa, Madagascar, Australia and the Lord Howe, Norfolk and Kermadec Is. Some species are common and occur almost throughout tropical Indomalesia or are widespread in Africa; others are rare and with a narrow range, for example restricted to one or a few oceanic islands. Each of the taxa occurring in the Old World is described and illustrated, habitats and geographical ranges are indicated, conservation status is discussed on the basis of our impression of old and new collecting activity, and distributions are mapped. The following new taxa are described: P. tsaratananensis Friis & Wilmot Dear from Madagascar, P. herpetophyton Friis & Wilmot‐Dear from the Comoro Is., and P. zeylanica subsp. calcicola Friis & Wilmot‐Dear and P. thailandica Friis & Wilmot‐Dear, both from southern Thailand. A new name, P. variifolia Friis & Wilmot‐Dear, is proposed for P. heterophylla (Blume) Wedd., nom. illeg. The following new combinations are published here: P. australis (Endl.) Friis & Wilmot‐Dear, P. sanguinea (Blume) Merr. var. formosana (Li) Friis & Wilmot‐Dear, P. sanguinea (Blume) Merrill var. cinerascens (Blume) Friis & Wilmot‐Dear, P. mixta Solms var. shirensis (Rendle) Friis & Wilmot‐Dear, P. hirta (Blume) Hasskarl var. parvifolia (Wight) Friis & Wilmot‐Dear, P. pentandra (Roxb.) Benn. & R. Br. subsp. wightii (Benn. & R. Br.) Friis & Wilmot‐Dear. and subsp. wightii (Benn. & R. Br.) Friis & Wilmot‐Dear var. gracilis (Miq.) Friis & Wilmot‐Dear. The following taxa are reduced to synonymy for the first time: Pouzolzia argenteonitida W.‐T. Wang, P. bracteosa Friis, P. calophylla W.‐T. Wang & C.‐J. Chen, P. guineensis Benth. var. seyrigii Leandri, P. guineensis Benth. var. madagascariensis Wedd., P. baronii Leandri, and P. auriculata Wight.     

Go forth,evolve and prosper: the genetic basis of adaptive evolution in an invasive species

Invasive species stand accused of a familiar litany of offences, including displacing native species, disrupting ecological processes and causing billions of dollars in ecological damage (Cox 1999 ). Despite these transgressions, invasive species have at least one redeeming virtue – they offer us an unparalleled opportunity to investigate colonization and responses of populations to novel conditions in the invaded habitat (Elton 1958 ; Sakai et al. 2001 ). Invasive species are by definition colonists that have arrived and thrived in a new location. How they are able to thrive is of great interest, especially considering a paradox of invasion (Sax & Brown 2000 ): if many populations are locally adapted (Leimu & Fischer 2008 ), how could species introduced into new locations become so successful? One possibility is that populations adjust to the new conditions through plasticity – increasing production of allelopathic compounds (novel weapons), or taking advantage of new prey, for example. Alternatively, evolution could play a role, with the populations adapting to the novel conditions of the new habitat. There is increasing evidence, based on phenotypic data, for rapid adaptive evolution in invasive species (Franks et al. 2012 ; Colautti & Barrett 2013 ; Sultan et al. 2013 ). Prior studies have also demonstrated genetic changes in introduced populations using neutral markers, which generally do not provide information on adaptation. Thus, the genetic basis of adaptive evolution in invasive species has largely remained unknown. In this issue of Molecular Ecology, Vandepitte et al. ( 2014 ) provide some of the first evidence in invasive populations for molecular genetic changes directly linked to adaptation.     

Presence of Anopheles culicifacies B in Cambodia established by the PCR-RFLP assay developed for the identification of Anopheles minimus species A and C and four related species

Abstract A polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP) assay developed for identification of five species of the Anopheles minimus Theobald group and a related mosquito species of the Myzomyia Series (Diptera: Culicidae) was applied to morphologically identified adult female specimens collected in Ratanakiri Province, north‐eastern Cambodia. In addition to finding An. aconitus Dönitz, An. minimus species A and An. pampanai Büttiker & Beales, some specimens showed a new restriction banding pattern. Siblings of specimens that exhibited this new PCR‐RFLP pattern were morphologically identified as An. culicifacies James sensu lato. Based on nucleotide sequences of the ribonuclear DNA internal transcribed spacer 2 region (ITS2) and the mitochondrial cytochrome oxidase I gene (COI), these specimens were recognized as An. culicifacies species B (sensu Green & Miles, 1980 ), the first confirmed record of the An. culicifacies complex from Cambodia. This study shows that the PCR‐RFLP assay can detect species not included in the initial set‐up and is capable of identifying at least seven species of the Myzomyia Series, allowing better definition of those malaria vector and non‐vector anophelines in South‐east Asia.     

On the nomenclature of <Emphasis Type="Italic">Arctia ornata</Emphasis> Staudinger, 1896 (Lepidoptera,Arctiidae)

The nomenclatural history of Callarctia ornata Packard, 1864 and Arctia ornata Staudinger, 1896 is discussed. Both these nominal taxa are shown to be neither primary nor secondary homonyms. The nomenclature act of O. Sotavalta dealing with the homonymisation of Arctia ornata Staudinger 1896 should be considered as inadequate to the rules of the International Code of Zoological Nomenclature. The nominal taxon, Arctia ornata Staudinger, 1896, should be considered as valid.     

Taxonomic studies on Zingiber (Zingiberaceae) in China IV: Z. pauciflorum sp. nov. from Yunnan

Zingiber pauciflorum L.Bai, ?korni?k., D.Z.Li & N.H.Xia (Zingibereae, Zingiberaceae), a new species from southern Yunnan, China, is described and colour plates are provided. It belongs to Z . sect. Cryptanthium Horan. and is compared with three similar species, namely Z. tenuifolium L.Bai, ?korni?k. & N.H.Xia, Z. smilesianum Craib and Z. yunnanense S.Q.Tong & X.Z.Liu. A colour plate of the most similar species, Z. smilesianum is also provided for comparison.     

A review of the genus Eristena Warren in China (Lepidoptera: Crambidae: Acentropinae)

The larvae of three known species of Callibaetis are described here for the first time: C. gonzalezi (Navás), C. pollens Needham &; Murphy and C. sellacki (Weyenbergh). The larva of C. willineri Navás is resdescribed and the larva of C. guttatus Navás is revised and discussed. The diagnoses of the adults are also provided.     

Morphological and allozyme diversity in the Hieracium nigrescens group (Compositae) in the Sudety Mountains and the Western Carpathians

The overall pattern of morphological variation and genetic diversity (allozyme analysis) was studied in the Hieracium nigrescens group (H. nigrescens s.l., H. alpinum ≥ H. murorum) in the Sudety Mountains and the Western Carpathians. A morphological analysis was performed on 180 plants from 12 populations belonging to six a priori distinguished taxa. Altogether, 25 characters were measured or scored. Morphometric (canonical discriminant analysis) data separated five taxa, evaluated here at the species rank: H. chrysostyloides, H. decipiens, H. nigrescens (all from the Sudety Mountains), H. jarzabczynum, and H. vapenicanum (the Western Carpathians). A distinct local population from Mount Babia hora (the Western Carpathians) comprised a further possible taxon, given the preliminary name ‘H. babiagorense’. Genetic diversity was studied in 17 populations of H. chrysostyloides, H. decipiens, H. jarzabczynum, H. nigrescens, H. vapenicanum and ‘H. babiagorense’ using five enzyme systems. All a priori recognized species were proved to be genetically homogeneous, each consisting of one unique multilocus allozyme genotype, except ‘H. babiagorense’ which shared the same genotype with H. jarzabczynum. For the first time, a chromosome number is reported for H. vapenicanum (2n = 3x = 27) and previously published numbers were confirmed for H. chrysostyloides (2n = 5x = 45), H. decipiens (2n = 4x = 36), H. jarzabczynum (2n = 4x = 36), H. koprovanum (2n = 4x = 36), and H. nigrescens (2n = 4x = 36). All species have been shown to be endemic to either the Sudety Mountains or the Western Carpathians. Except for the species studied, two further ones (H. apiculatum, H. nivimontis) are recognized in the area, giving a total of seven species from the Hieracium nigrescens group in the area studied. The morphologically slightly different local population from Mount Babia hora/Babia Góra (‘H. babiagorense’) requires further study. Two new combinations are proposed: Hieracium jarzabczynum (Paw?. & Zahn) Mráz & Chrtek f. and Hieracium vapenicanum (Lengyel & Zahn) Chrtek f. & Mráz. © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society, 2007, 153 , 287–300.     

Notes on Neotropical Zoraptera, with descriptions of two new species

Characters used un specific identification of Zoraptera are briefly discussed. A list of Neotropical species is given, and the difficulties of associating sexes of some species outlined. Two new species are described and figured (Zorotypus weidneri sp.n., ♂, ♀, Brazil; Z.hamiltoni sp.n., ♂, ♀, Colombia) and additional records and information given on Z.shannoni Gurney (♂, Brazil) and Z.huxleyi Bolivar y Pieltain & Coronado G (♂, ♀, recorded from Brazil for the first time).     

Haplodontium zangii X.R.Wang & J.C.Zhao,sp. nov. (Bryaceae,Bryopsida) from Xizang,China

Haplodontium zangii X.R.Wang &; J.C.Zhao, a new moss species from Xizang, China, is described and illustrated. Previously, specimens of H. zangii have been identified as Mielichhoferia himalayana Mitt. However, H. zangii is distinctly different from M. himalayana in having excurrent costae with short awns (vs long denticulate awns), short-pyriform capsules, 0.8–1?mm (vs long-pyriform capsules, 2.5–3?mm), and densely papillose exostome teeth (vs smooth or vertically striped exostome teeth). Haplodontium zangii is similar to H. macrocarpum (Hook.) J.R.Spence, which was traditionally placed in Mielichhoferia Nees &; Hornsch. as M. macrocarpa (Hook.) Bruch &; Schimp. The main differences between H. zangii and H. macrocarpum are in the morphology of the leaves, capsules, guide cells, and stomata. Mielichhoferia himalayana and another Chinese species of Mielichhoferia, M. sinensis Dix., are also transferred to Haplodontium Hampe, a new genus in the bryoflora of China, as H. himalayanum (Mitt.) X.R.Wang &; J.C.Zhao and H. sinensis (Dix.) X.R.Wang &; J.C.Zhao. A morphological comparison and a key to the three species of Haplodontium in China as well as to H. macrocarpum, a species that is likely to be found in China, are provided.     

New Records of Noctuoid Moths (Lepidoptera,Noctuoidea) in the Baikal Region

The results of long-term faunistic studies of the noctuoid moths in the Baikal region and the literature review are presented. An annotated check-list including 83 species of the families Notodontidae, Erebidae, Nolidae, and Noctuidae is given. Data on the previous records of the species from the study region are given. The Noctuoidea fauna of Irkutsk Province comprises 462 species, that of the Republic of Buryatia, 419 species, and that of the Baikal region as a whole, 510 species. The distribution limits are expanded for 17 species of the Noctuoidea complex: the new eastern range boundary is established for 11 species of Erebidae and Noctuidae, and the new western one is established for 5 representatives of Notodontidae, Erebidae and Noctuidae. Two species, Actebia confinis (Staudinger, 1881) and Actebia confusa (Alphéraky, 1882), are new to the Russian fauna. The trophic associations of Phidrimana amurensis (Staudinger, 1892) are established: the larvae of this Euro-Siberian species feed on the leaves of different species of elms (Ulmus japonica Rehder, Ulmus pumila L.). Three noctuid species, Calyptra lata (Butler, 1881), Bryophila granitalis (Butler, 1881) and Cosmia trapezinula (Filipjev, 1927), with large disjunctions of their ranges are reported; these moths are apparently relicts of the Atlantic Period of the Holocene.     

Taxonomic studies on Zingiber (Zingiberaceae) in China VI: Z. leucochilum,a new species with running rhizome from Sichuan

Zingiber leucochilum L.Bai, ?korni?k. & N.H.Xia (Zingibereae, Zingiberaceae), a new species from southeastern Sichuan, China, is described and illustrated with a colour plate. Notes on ecology, distribution and a preliminary IUCN conservation assessment are also provided. The new species is assigned to Z . sect. Cryptanthium Horan. and compared to five morphologically similar species from China which share the characteristic well‐elongated and running rhizome, namely, Z. emeiense Z.Y.Zhu, Z. leptorrhizum D.Fang, Z. pauciflorum L.Bai, ?korni?k., D.Z.Li & N.H.Xia, Z. smilesianum Craib and Z. yunnanense S.Q.Tong & X.Z.Liu. A key to the above six species is provided and their distributions are mapped.