Pythiopina,an enigmatic subtribe of darkling beetles (Coleoptera: Tenebrionidae: Pedinini): taxonomic revision,microtomography, ecological niche models and phylogenetic position

Morphological, anatomical, and distributional data concerning the S outh A frican endemic beetle subtribe P ythiopina (T enebrionidae: P edinini) are revised. Five species, representing two genera, are recognized. Included in this total is one new species (Meglyphus mariae K amiński sp.n. ). The following species are placed in synonymy: Meglyphus ciliatipes [=Meglyphus calitzensis syn.n. ]; Meglyphus laenoides [=Meglyphus andreaei syn.n. ; =Meglyphus namaqua syn.n. ]. Microtomographic models for all valid P ythiopina species, including the holotype of the newly described species, are presented and analysed. Endoskeleton morphology (specifically characters of the tentorium and metendosternite) proved to be informative at the specific and generic levels. An identification key is provided to all known species of the subtribe. Environmental niche models are presented for the majority of species. A molecular phylogeny of P edinini based on six genetic loci (28S : D 1–D 3 region; 28S : D 4–D 5 region, COII , A rgK , CAD 2, wg) was also produced to explore the phylogenetic position of P ythiopina. This analysis is the first to include representatives of all seven subtribes of P edinini, and supports a sister relationship between P ythiopina and the P alaearctic subtribe D endarina. Results also suggest the existence of a second pair of sister taxa within P edinini (in addition to M elambiina) with an amphitropical A frican distribution. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:285AD87A‐46B1‐4FE9‐BC57‐949EA1F70D49 .     

Towards a natural classification of the subtribe Philonthina (Coleoptera: Staphylinidae: Staphylinini): a phylogenetic analysis of the Neotropical genera

Philonthina, the largest subtribe of the rove beetle tribe Staphylinini, is a hyperdiverse group in the Neotropical Region, accounting for about half of the genera of the subtribe. Despite such diversity, Neotropical Philonthina have never been analysed phylogenetically, deterring formulation of a modern classification of the Staphylinini. A cladistic analysis of Neotropical Philonthina was performed based on 110 morphological characters and 77 terminal taxa. Representatives of Philonthina from other regions and other main lineages of Staphylinini, Arrowinini and Platyprosopini were included to test their relationships with Neotropical Philonthina. The major results are the monophyly of 11 of the 17 endemic Neotropical genera of Philonthina, the placement of Holisus Erichson (Hyptiomina) into this clade showing a sister group relationship to myrmecophile genera, and the position of Erichsonius Fauvel outside of Philonthina within Staphylinini. Six of the current seven species of Endeius Coiffait & Sáiz group with Neotropical species of Philonthus Stephens. The separation of Gondwana about 65 my and major landscape modifications in the vast interior of northern South America during the past 25 my is proposed to explain the evolution of the endemic Neotropical genera of Philonthina. The following taxonomic changes are proposed: Erichsonius Fauvel, 1874 now placed as incertae sedis in Staphylinini; Endeius Coiffait & Sáiz, 1968, n.syn. of Philonthus Stephens, 1929 and Endeius nitidipennis (Solier, 1849) placed as incertae sedis in Philonthina. The following new combinations are proposed: Philonthus franzi (Sáiz, 1971), comb.n. , Philonthus loensis (Coiffait & Sáiz, 1968), comb.n. , Philonthus lugubris (Sáiz, 1971), comb.n. , Philonthus ovaliceps (Coiffait, 1981), comb.n. , Philonthus punctipennis (Solier, 1849), comb.res. and Philonthus subpunctipennis (Coiffait & Sáiz, 1968), comb.n. Philonthus herberti, n.nov., is proposed for Philonthus franzi Schillhammer, 1998 , which is a junior secondary homonym of Philonthus franzi (Sáiz, 1971).     

A phylogenetic study of the Thygater‐Trichocerapis group and new scopes for the subgenera of Thygater Holmberg, (Hymenoptera,Apidae)

The bee tribe Eucerini is a large monophyletic taxon occurring in all continents, except Oceania and Antarctica, but far more diverse in the Americas and, especially, in the Neotropics. The phylogenetic relationships within its subtribe Eucerina, which contains the bulk of Eucerini diversity, is poorly understood, this being especially true for the relationships among its Neotropical representatives, which have been poorly represented in all phylogenetic studies, including Eucerini, to date. This leads to a generalized lack of confidence on the monophyly of the groups currently accepted as genera and subgenera. Here, a phylogenetic study based on three molecular markers (COI, 18S, and 28S, totalling about 1700 bp) and 58 morphological characters is presented as a contribution to the understanding of the relationships of the so‐called Thygater‐Trichocerapis group, and especially of the genus Thygater Holmberg, which has not previously been extensively sampled. Representatives of Trichocerapis, including its monotypic subgenus T. (Dithygater), are included for the first time in a phylogenetic study. The main results were: (i) support for the monophyly of the Thygater‐Trichocerapis group; (ii) support for the monophyly of Thygater; (iii) recognition of two main clades in Thygater, each one containing the type species of one of the previously recognized subgenera; and (iv) additional support for the position of Alloscirtetica as sister to all remaining Eucerina. Based on these results a redefinition of the scope of the two subgenera of Thygater is proposed, with changes in the subordination of three of its species, T. (Nectarodiaeta) chaetaspis comb.n. , T. (Nectarodiaeta) paranaensis comb.n. and T. (Thygater) mexicana comb.n.     

Systematics and cladistics of Megalostomis Chevrolat,and the biogeography of Clytrini (Coleoptera: Cryptocephalinae)

We present a cladistic analysis of the subtribe Megalostomina, a Neotropical group of ‘case‐bearer’ leaf beetles. A comparative study of the external and internal adult morphology of Clytrini was undertaken. New characters are described for the subtribe Megalostomina, from the internal sac of aedeagus, which provide a useful phylogenetic signal. More than 180 photographs illustrating the most important characters (74 characters and their respective states) used in the cladistic analysis are provided. The cladistic analysis of 57 terminal taxa and 95 characters was undertaken, under equal weights, and also using implied weights as a means to down‐weight homoplasious characters. We test the monophyly and explore intergeneric relationships of the subtribe Megalostomina, and reconstruct the relationships among the species of Megalostomis Chevrolat. The 42 species recognized can be assigned either to a group mostly containing species of North and Central America, or to a larger one of mostly South American species. Support is low, and the formal naming of groups is deferred pending a revision of all Megalostomina. We confirm the subgenera of Megalostomis of previous classifications are unnatural, and the following changes in the generic classification of the subtribe Megalostomina are proposed: Coleorozena Moldenke syn.n. of Coscinoptera Lacordaire; Coleothorpa Moldenke syn.n. of Coscinoptera Lacordaire; and Euryscopa (Coleoguerina) Moldenke syn.n. of Coscinoptera Lacordaire. Furthermore, six formerly recognized subgenera of Megalostomis are considered junior synonyms of Megalostomis Chevrolat: Megalostomis (Minturnia) Lacordaire syn.n. ; Megalostomis (Heterostomis) Lacordaire syn.n. ; Megalostomis (Scaphigenia) Lacordaire syn.n. ; Megalostomis (Snellingia) Moldenke syn.n. ; Megalostomis (Coleobyersa) Moldenke syn.n. ; and Megalostomis (Pygidiocarina) Moldenke syn.n. Thus, no subgenera are recognized within Megalostomis. Previous hypotheses on Clytrini biogeography were revisited in the light of new biogeographic and phylogenetic knowledge. We hypothesize an origin of Clytrini in tropical/subtropical Gondwana, when South America, Africa, Madagascar and India were connected. Changes in the configuration of the tectonic plates in the Cenozoic allowed the dispersal of Clytrina to the Palaearctic and Nearctic regions, and dispersion of Babiina and Megalostomina through the Nearctic region.     

Putting Parasemia in its phylogenetic place: a molecular analysis of the subtribe Arctiina (Lepidoptera)

Despite being popular among amateur and professional lepidopterologists and posing great opportunities for evolutionary research, the phylogenetic relationships of tiger moths (Erebidae: Arctiinae) are not well resolved. Here we provide the first phylogenetic hypothesis for the subtribe Arctiina with the basic aim of clarifying the phylogenetic position of the Wood Tiger Moth Parasemia plantaginis Hübner, a model species in evolutionary ecology. We sampled 89 species in 52 genera within Arctiina s.l., 11 species of Callimorphina and two outgroup species. We sequenced up to seven nuclear genes (CAD, GAPDH, IDH, MDH, Ef1α, RpS5, Wingless) and one mitochondrial gene (COI) including the barcode region (a total of 5915 bp). Both maximum likelihood and Bayesian inference resulted in a well‐resolved phylogenetic hypothesis, consisting of four clades within Arctiina s.s. and a clade comprising spilosomine species in addition to Callimorphina and outgroups. Based on our results, we present a new classification, where we consider the Diacrisia clade, Chelis clade, Apantesis clade, Micrarctia Seitz and Arctia clade as valid genera within Arctiina s.s., whereas Rhyparia Hübner syn.n. and Rhyparioides Butler syn.n. are synonymized with Diacrisia Hübner; Neoarctia Neumoegen & Dyar syn.n. , Tancrea Püngeler syn.n. , Hyperborea Grum‐Grshimailo syn.n. , Palearctia Ferguson syn.n. , Holoarctia Ferguson syn.n. , Sibirarctia Dubatolov syn.n. and Centrarctia Dubatolov syn.n. are synonymized with Chelis Rambur; Grammia Rambur syn.n. , Orodemnias Wallengren syn.n. , Mimarctia Neumoegen & Dyar syn.n. , Notarctia Smith syn.n. and Holarctia Smith syn.n. are synonymized with Apantesis Walker; and Epicallia Hübner syn.n. , Eucharia Hübner syn.n. , Hyphoraia Hübner syn.n. , Parasemia Hübner syn.n. , Pericallia Hübner syn.n. , Nemeophila Stephens syn.n. , Ammobiota Wallengren syn.n. , Platarctia Packard syn.n. , Chionophila Guenée syn.n. , Eupsychoma Grote syn.n. , Gonerda Moore syn.n. , Platyprepia Dyar syn.n. , Preparctia Hampson syn.n. , Oroncus Seitz syn.n. , Acerbia Sotavalta syn.n. , Pararctia Sotavalta syn.n. , Borearctia Dubatolov syn.n. , Sinoarctia Dubatolov syn.n. and Atlantarctia Dubatolov syn.n. are synonymized with Arctia Schrank, leading to 33 new genus‐level synonymies. Our focal species Arctia plantaginis comb.n. is placed as sister to Arctia festiva comb.n. , another widespread aposematic species showing wing pattern variation. Our molecular hypothesis can be used as a basis when adding more species to the tree and tackling interesting evolutionary questions, such as the evolution of warning signalling and mimicry in tiger moths.     

Systematic revision of Hoggicosa Roewer, 1960, the Australian ‘bicolor’ group of wolf spiders (Araneae: Lycosidae)

The Australian wolf spider genus Hoggicosa Roewer, 1960 with the type species Hoggicosa errans (Hogg, 1905) is revised to include ten species: Hoggicosa alfi sp. nov. ; Hoggicosa castanea (Hogg, 1905) comb. nov. (= Lycosa errans Hogg, 1905 syn. nov. ; = Lycosa perinflata Pulleine, 1922 syn. nov. ; = Lycosa skeeti Pulleine, 1922 syn. nov. ); Hoggicosa bicolor (McKay, 1973) comb. nov. ; Hoggicosa brennani sp. nov. ; Hoggicosa duracki (McKay, 1975) comb. nov. ; Hoggicosa forresti (McKay, 1973) comb. nov. ; Hoggicosa natashae sp. nov. ; Hoggicosa snelli (McKay, 1975) comb. nov. ; Hoggicosa storri (McKay, 1973) comb. nov. ; and Hoggicosa wolodymyri sp. nov. The Namibian Hoggicosa exigua Roewer, 1960 is transferred to Hogna, Hogna exigua (Roewer, 1960) comb. nov. A phylogenetic analysis including nine Hoggicosa species, 11 lycosine species from Australia and four from overseas, with Arctosa cinerea Fabricius, 1777 as outgroup, supported the monophyly of Hoggicosa, with a larger distance between the epigynum anterior pockets compared to the width of the posterior transverse part. The analysis found that an unusual sexual dimorphism for wolf spiders (females more colourful than males), evident in four species of Hoggicosa, has evolved multiple times. Hoggicosa are burrowing lycosids, several constructing doors from sand or debris, and are predominantly found in semi‐arid to arid regions of Australia. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 83–123.     

The West Indian species of Encyrtidae described by L. D. Howard, 1894 and 1897 (Hymenoptera, Chalcidoidea)

Abstract. The following species of encyrtids described by Howard (1894, 1897) from St Vincent and Grenada are redescribed or dealt with in some other way. The current generic placements and synonymies are indicated in parentheses. Archinus occupants (Archinus), Aphycus amoenus (Metaphycus comb.n.), Aratus scutellatus (= brasiliensis Subba Rao syn.n., Zeteticontus), Blastothrix insolitus ( Anagyrus comb .n. ), Bothriothorax insularis (Zeteticontus), Cerchysius terebratus (Anagyrus), Cerchysius pulchricornis (Anagyrus), Chieloneurus funiculus (= cupreicollis Ashmead syn.n., Cheiloneurus), Cheiloneurus nigrescens (= longisetaceus De Santis syn.n., Cheiloneurus), Copidosoma diversicomis (Apoanagyrus comb.n.), Encyrtus argentipes (Zaomma), Encyrtus crassus (= Encyrtus gargaris Walker syn.n. = Giraultella lopesi Costa Lima & Ferreira syn. n, Coelopencyrtus comb.n.), Encyrtus conformis (Encyrtus), Encyrtus convexus (= Encyrtus nitidus (Howard) syn. n.), Encyrtus flaviclavus (Encyrtus), Encyrtus hirtus (Hunterellus comb.n.), Encyrtus moderatus (= Adelencyrtus femoralis Compere & Annecke syn. n. = Adelencyrtus miyarai Tachikawa syn. n., Adelencyrtus comb.n.), Encyrtus nitidus (= Protyndarichus proximus De Santis syn. n., Protyndarichus comb.n.), Encyrtus quadricolor (Encyrtus), Encyrtus rotundiformis (Psyllaephagus comb.n.), Encyrtus sordidus (Forcipestricis comb.n.), Encyrtus submetallicus (Ooencyrtus), Habrolepoidea glauca (Habrolepoidea) and Homalopoda cristata (Homalopoda). Xiphomastix De Santis is synonymized with Anagyrus Howards (syn. n.), both included species ( X. nigriceps De Santis and X. bellator De Santis) being transferred to the latter. Propsyllaephagus Blanchard is synonymized with Psyllaephagus Ashmead (syn.n), Aratiscus laevigatus De Santis is transferred to Zeteticontus Silvestri (comb n.) and a key to the South American species of the genus is provided.     

Revision of the section Anillochlamys Jeannel, 1909 (Coleoptera: Leiodidae: Cholevinae: Leptodirini)

The taxonomy of the Iberian Leptodirini species of the section Anillochlamys Jeannel, 1909 has been revised. The proposed classification is based on the study of the genital structures of both sexes, in particular the internal sac of the aedeagus. According to the different models of internal sacs, the following genera, species and subspecies are identified: genus Anillochlamys Jeannel, 1909: A. aurouxi Español, 1965, A. bueni Jeannel, 1909 (= A. avariae Comas, 1977 n.syn.), A. cullelli Lagar, 1978, A. moroderi Bolívar, 1923 (= A. negrei Comas, 1990 n. syn.), A. subtruncatus Jeannel, 1930 (= A. baguenai Jeannel, 1930) and A. tropicus (Abeille, 1881) (= Adelops hispanicus Ehlers, 1893; A. tropicus var. apicalis Jeannel, 1909); genus Paranillochlamys Zariquiey, 1940: P. catalonicus (Jeannel, 1913), P. urgellesi (Español, 1965) and P. velox Zariquiey, 1940 (= P. velox montadai Lagar, 1963 n. syn.); genus Pseudochlamys Comas, 1977: P. raholai (Zariquiey, 1922) (= Anillochlamys raholai luis-bofilli Zariquiey, 1940 n. syn.); genus Spelaeochlamys Dieck, 1870 (= Typhlochlamys Español, 1975 n.syn.): S.bardisai (Español, 1975) (= Typhlochlamys escolai Comas, 1978 n. syn.), S. ehlersi Dieck, 1870 and S. ehlersi verai Comas, 1977 n. stat.     

Febraina: a new subtribe of Alticini with cladistic analysis based on morphology (Coleoptera: Chrysomelidae: Galerucinae)

A new subtribe Febraina subtr.n. is established with Febra Clark designated as the type genus. Cladistic analysis based on morphological characters is carried out to reveal the composition of a new subtribe and to test its monophyly. Subtribe includes the following genera: Chilocoristes Weise; Halticorcus Lea; Setsaltica Samuelson; Maaltica Samuelson; Axillofebra Samuelson; Profebra Samuelson. Bionomical features of the genera of the subtribe are summarised. The syndrome of hemisphery is recorded for the genera of the subtribe, and morphological transformation resulting in hemisphery is described and discussed. Correspondence between direction of morphological transformation, phylogenetic arrangement of genera, and distributional pattern is recorded and discussed.     

Generic revision and phylogeny of Microweiseinae (Coleoptera: Coccinellidae)

The monophyly and phylogenetic relationships of the subfamily Microweiseinae were investigated. Twenty‐three in‐group taxa, representing all known genera of Microweiseinae (except for Microcapillata Gordon) were included in a cladistic analysis, based on 45 adult morphological characters. The parsimony analysis of the resulting data matrix supported the monophyly of Microweiseinae, Carinodulini, Serangiini and Microweiseini (inclusive of Sukunahikonini). The recognition of Sukunahikonini renders Microweiseini paraphyletic, and consequently both tribes were synonymized, retaining Microweiseini as a senior family‐group name ( syn.n. ). Genera and tribes of Microweiseinae are diagnosed thoroughly, illustrated and keys to their identification are provided. The following nomenclatural changes were made: Hikonasukuna Sasaji and Orculus Sicard are synonymized with Scymnomorphus Weise ( syn.n. ); Gnathoweisea Gordon is synonymized with Microweisea Cockerell ( syn.n. ); Hikonasukuna monticola Sasaji and Orculus castaneus Sicard are transferred to Scymnomorphus ( comb.n. ); Smilia planiceps Casey, Gnathoweisea hageni Gordon, Gnathoweisea ferox Gordon, Gnathoweisea micula Gordon and Gnathoweisea texana Gordon are transferred to Microweisea ( comb.n ). Three new genera are described: Allenius gen.n. for Allenius californianus sp.n. (type species) from Mexico and Allenius iviei sp.n. from U.S.A.; Gordoneus gen.n. (type species Gnathoweisea schwarzi Gordon from U.S.A.); and Cathedrana gen.n. (type species Cathedrana natalensis sp.n. from South Africa). The first African member of Carinodulini, Carinodulina ruwenzorii sp.n. is described. The genera Microweisea, Coccidophilus, Serangium and Delphastus are well‐known predators of sternorrynchous Hemiptera, such as scale insects (Diaspididae) and whiteflies (Aleyrodidae), and play a significant role in agricultural ecosystems as biocontrol agents. Host data and biological records are summarized for each genus.     

Revision and phylogeny of Syrphetodes (Coleoptera: Ulodidae): implications for biogeography,alpinization and conservation

The genus Syrphetodes Broun is revised to include a total of 13 species. Most of the species are restricted in their distributions, are rarely collected and have been attributed conservation status in New Zealand. Eleven species are described as new: three from Northland (S. relictus sp.n ., Te Paki; S. insularis sp.n. , Three Kings Islands; S. magnus sp.n. , Hokianga), one from the central North Island (S. obtusus sp.n. ), one from Central Otago (S. nunni sp.n. , Waikaia Bush), and seven from the southern Alps (S. cirrhopogon sp.n. , Aspiring National Park; S. occiduus sp.n. , Westland; S. melanopogon sp.n. , Mt Dewar, Paparoa Range; S. defectus sp.n. , northern Paparoa Range; S. marrisi sp.n. , Mt Domett, Northwest Nelson; S. carinatus sp.n. , Victoria Range). Eleven synonymies are proposed: S. crenatus Broun (= S. dorsalis Broun, syn.n .), S. marginatus Pascoe (= S. bullatus Sharp, syn.n. ; S. sylvius Broun, syn.n. ; S. cordipennis Broun, syn.n. ; S. punctatus Broun, syn.n. ; S. simplex Broun, syn.n. ; S. nodosalis Broun, syn.n. ; S. truncatus Broun, syn.n. ; S. variegatus Broun, syn.n. ; S. pensus Broun, syn.n. ; S. thoracicus Broun, syn.n. ). The phylogenetic relationships among the species were reconstructed using morphological (25 adult characters) and DNA sequence (nuclear 28S rDNA and mitochondrial cytochrome c oxidase subunit I) data. A morphological analysis rooted with Trachyderastes resulted in a split between lowland and high‐altitude species and a well‐supported group from Northland. Molecular trees rooted with representatives of Trachyderastes Kaszab (New Caledonia), Meryx Latrielle (Australia), Ulodes Erichson (Australia) and three New Zealand genera (Arthopus Sharp, Brouniphylax Strand, Exohadrus Broun) resulted in the following tree: ((Ulodes, Brouniphylax) (Exohadrus, Arthopus)) (Syrphetodes (Meryx, Trachyderastes)). Species relationships within Syrphetodes included a strongly supported northern North Island clade and an alpine clade either as sister taxon to S. crenatus and S. marginatus or sister remaining lowland lineages. Combined phylogenetic analyses also showed paritial congruence with separate partitions. The distributions of the lowland species, in particular those from the North Island, correspond to islands that existed in the Pliocene. The alpine, black‐coloured lineage, found above the treeline, is monophyletic based on several characters (e.g. lack of abdominal flanges and reduced scalation) and, in some reconstructions, the tan‐coloured S. cirrhopogon is sister taxon to the remaining black‐coloured species. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:697E68E8‐EE90‐46C1‐A009‐78A794E0EF4F .     

Phylogenetic Systematics and Biogeography of the Neoephemeridae (Ephemeroptera: Pannota)

A revision of species of the pannote Holarctic and Oriental mayfly family Neoephemeridae is presented. Three genera are recognized in a strictly phylogenetic classification. Potamanthellus [=Neoephemeropsis Ulmer syn. n.] includes P. caenoides (Ulmer) comb. n., P. amabilis (Eaton) [=N. cuaraoensis Dang syn. n.], P. ganges sp. n., P. chinensis (Hsu) [=P. rarus (Tiunova and Levanidova) syn. n.], P. edmundsi sp. n., and the Oligocene fossil Potamanthellus rubiensis Lewis. Neoephemera [=Leucorhoenanthus Lestage syn. n.] includes N. maxima (Joly), N. purpurea (Traver), N. youngi Berner, N. bicolor McDunnough, and N. compressa Berner. Ochernova gen. n., includes O. tshernovae (Kazlauskas) comb. n. Taxa are described, illustrated and keyed. Species cladistics and biogeography are presented.     

Phylogenetic reassessment and biogeography of the Ectateus generic group (Coleoptera: Tenebrionidae: Platynotina)

Owing to the reinterpretation of its morphological synapomorphies, the taxonomic composition of the Ectateus generic group had been ambiguous. The present study scrutinized all existing taxonomic concepts of the group based on a cladistic analysis of the adult morphology of all of the Afrotropical platynotoid Platynotina genera. The phylogenetic relationships were reconstructed using parsimony and Bayesian inference. The results show that all previous taxonomic concepts of the Ectateus generic group concerned paraphyletic entities. The cladistic analysis revealed the following synapomorphies for the taxon: (1) presence of basal indentations of the pronotal disc, (2) ratio of prothorax width to its maximal height > 6.0, and (3) ratio of maximal height of the prothorax to total height < 0.3. Moreover, phylogenetic studies revealed the existence of the Upembarus generic group, a sister‐taxon group to the Ectateus generic group, within the Afrotropical platynotoid Platynotina. Autapomorphic and synapomorphic character mapping show that several taxonomic and nomenclatural changes are needed to consider the particular generic‐level entities traditionally assigned to Afrotropical platynotoid Platynotina as monophyletic lineages. The following taxonomic and nomenclatural adjustments are made in this paper: P teroselinus gen. nov. is erected to accommodate a single species that was previously assigned to Zidalus: Pteroselinus insularis comb. nov. Additionally, the following synonymies are proposed: Anchophthalmops (= Platykochius syn. nov. ), Angolositus (= Aberlencus syn. nov. , = Platymedvedevia syn. nov. ), Glyptopteryx (= Microselinus syn. nov. , = Quadrideres syn. nov. , = Synquadrideres syn. nov. ). In addition, Kochogaster is lowered in rank and is treated as one of the subgenera of Anchophthalmus. Moreover, Pseudoselinus is treated as a subgenus of Upembarus. An identification key to all Afrotropical platynotoid Platynotina genera and subgenera is presented. Zoogeographical analyses revealed the following dispersal barriers for the Ectateus generic group: (1) the Sahara (northern barrier); (2) the dry ecosystems of Botswana, Namibia, and South Africa (southern barrier); and (3) the Congolian rainforests (internal distributional gap). The ancestor of the taxon probably originated in East African ecoregions that predominantly contained wattletrees (acacias) and Commiphora Jacq. Moreover, past climate changes seem to have had a great impact on the observed generic distribution. © 2015 The Linnean Society of London     

A revision of the Oriental stonefly genus Phanoperla (Plecoptera: Perlidae)

The genus Phanoperla (=Dyaperla Banks, 1939) (Plecoptera: Perlidae: Perlini) is revised and generic diagnoses are provided for adults and larvae. Diagnostic and constitutive characters of the tribe Neoperlini are discussed, and Chinoperla Zwick, 1980, is shown to be the closest relative of Phanoperla. Many past misidentifications of Phanoperla species have been corrected by the use of characters recently recognized as important, namely the structure of the internal genitalia of male and female specimens and particularly the complex pattern of spines on the male penial sac made visible by eversion of this structure, and details of sculpturing of the egg chorion.
The following species of Phanoperla are recognized: amorpha sp.n.; anomala (Banks, 1939); bakeri (Banks, 1924); ceylonica Kawai, 1975; comuta sp.n.; flaveola (Klapálek, 1921), comb.n. ( =clarissa (Banks, 1913), syn.n.), (=Neoperla hageni Banks, 1920, syn.n.), (= N.consimilis Banks, 1924, syn.n.); guttata sp.n.; himalayana Zwick, 1977 (= siwalika Harper, 1977); limosa (Hagen, 1858); maculata sp.n.; maindroni (Navas, 1926), comb.n.; malayana sp.n.; minutissima (Enderlein, 1909); nana sp.n.; nervosa Banks, 1939; nuwara Kawai, 1975; omega sp.n.; pallipennis (Banks, 1938); parva sp.n.; pumilio (Klapálek, 1921), comb.n.; peniculus Kawai, 1969a; schmidi sp.n.; sertispina Jewett, 1975; srilanka sp.n.; sumatrae sp.n.; testacea (Hagen, 1858); wedda sp.n. P.claggi (Banks, 1938) is a nomen nudum.
All species are (re-)described and figured; all primary types have been examined. A key to species is provided. Most species can be assigned to one of seven species groups which are defined.
Phanoperla is endemic to the Oriental Region. Species groups are generally widespread, but individual species are in most cases known only from restricted areas.     

Revised systematics and biogeography of ‘Quediina’ of sub‐Saharan Africa: new phylogenetic insights into the rove beetle tribe Staphylinini (Coleoptera: Staphylinidae)

Abstract Quediina, a mega‐diverse conventional subtribe of the rove beetle tribe Staphylinini, is remarkably species rich in the north and south temperate regions of the world. Tropical faunas of this group, and the fauna of the entire Afrotropical biogeographical region (= Ethiopian region, = sub‐Saharan Africa), in contrast, are remarkably poor. The taxonomic study of the quediine genera of Staphylinini from the Afrotropical region reveals misidentifications for many of them. Their phylogenetic study demonstrates polyphyly of Quediina and reveals a new evolutionary pattern for the entire tribe Staphylinini. In particular, the formerly quediine genera Euristus Fauvel, 1899 , Ioma Blackwelder, 1952, Natalignathus Solodovnikov, 2005 , all endemic in the Afrotropical region, belong to the non‐related ‘Staphylinina’, ‘Philonthina propria’ and ‘Tanygnathinina sensu novo’ lineages of Staphylinini, respectively. Contrary to earlier records, the genus Quedius Stephens, 1929 does not occur in Africa south of Sahara: Quedius angularis Cameron, 1948 and Quedius cinctipennis Cameron, 1951 are moved to the genus Philonthus Stephens, 1829. The same is established for the Asian genus Algon Sharp, 1874, formerly for a long time associated with Quediina: African species Algon robustus Wendeler, 1928 is moved to the genus Moeocerus Fauvel, 1899 (here in the ‘Philonthina propria’ lineage); and the misidentification of Algon africanus Bernhauer, 1915, a species that probably belongs to a new genus, is discussed. The phylogenetic affiliation of Afroquedius Solodovnikov, 2006 , a South African endemic, is still ambiguous. Overall, the formerly seen bipolar distribution pattern for the ‘Quediina’ is demonstrated to be an artefact, not a reality to explain. Historical biogeographical explanations are proposed for some of the Afrotropical endemics, partly as an attempt to apply biogeography as an external criterion for the evaluation of the new phylogenetic pattern revealed for Staphylinini. The monotypic genera Euristus and Ioma, as well as Heterothops megalops Cameron, 1959 , the only representative of this widespread genus in the Afrotropical region, are redescribed. Limits and synapomorphies of the genus Heterothops are discussed. The following new combinations and new names are proposed: Philonthus cinctipennis ( Cameron, 1951 ) comb.n. (preoccupied by Philonthus cinctipennis Fauvel, 1875), here replaced by Philonthus pseudoquedius Solodovnikov nom.n. ; Philonthus angularis ( Cameron, 1948 ) comb.n. ; Moeocerus robustus ( Wendeler, 1928 ) comb.n. [preoccupied by Moeocerus robustus (Gestro, 1881)], here replaced by Moeocerus wendeleri Solodovnikov nom.n. A lectotype is designated for Heterothops megalops Cameron, 1959 .     

Stenotaenia Koch, 1847: a hitherto unrecognized lineage of western Palaearctic centipedes with unusual diversity in body size and segment number (Chilopoda: Geophilidae)

Based on morphological evidence, we newly define the genus Stenotaenia Koch, 1847 (=Scnipaeus Bergsøe & Meinert, 1866; =Simophilus Silvestri, 1896; =Onychopodogaster Verhoeff, 1902; =Insigniporus Attems, 1903; =Notadenophilus Verhoeff, 1928; =Bithyniphilus Verhoeff, 1941; =Schizopleres Folkmanova, 1956; =Euronesogeophilus Matic, 1972; all syn. nov. ) as including the following 15 species: Stenotaenia linearis (Koch, 1835) (=Geophilus simplex Gervais, 1835; =Geophilus brevicornis Koch, 1837; =Scnipaeus foveolatus Bergsøe & Meinert, 1866; =Himantarium caldarium Meinert, 1886 syn. nov. ; =Geophilus (Geophilus) linearis var. polyporus Verhoeff, 1896 syn. nov. ; =Geophilus ormanyensis Attems, 1903 syn. nov. , after lectotype designation; =Insigniporus acuneli C?pu?e, 1968 syn. nov. ) from central and northern Europe; Stenotaenia frenum (Meinert, 1870) from northern Africa; Stenotaenia romana (Silvestri, 1895) (=Geophilus silvestrii Verhoeff, 1928 syn. nov. ) and Stenotaenia sorrentina (Attems, 1903) (=Geophilus forficularius Fanzago, 1881 syn. nov. ; =Geophilus linearis abbreviatus Verhoeff, 1925 syn. nov. ) from the Italian peninsula and Sardinia; Stenotaenia antecribellata (Verhoeff, 1898) (=Simophilus albanensis Attems, 1929 syn. nov. ), Stenotaenia cribelliger (Verhoeff, 1898), Stenotaenia palpiger (Attems, 1903), Stenotaenia rhodopensis (Kaczmarek, 1970), and Stenotaenia sturanyi (Attems, 1903) from the Balkan peninsula; Stenotaenia naxia (Verhoeff, 1901) (=Geophilus graecus Verhoeff, 1902) from the Aegean islands; Stenotaenia asiaeminoris (Verhoeff, 1898) and Stenotaenia bosporana (Verhoeff, 1941) from Anatolia; Stenotaenia giljarovi (Folkmanova, 1956) from western Caucasus; Stenotaenia fimbriata (Verhoeff, 1934) and Stenotaenia palaestina (Verhoeff, 1925) from Palestine; with the only exception of S. linearis, all of these binomens are comb. nov. In Stenotaenia, a strongly conserved overall morphology is matched by an unusual interspecific variation in both the body size of fully grown specimens (from 1.7 cm in S. romana to 7.7 cm in S. sturanyi) and the number of leg‐bearing segments (from 43 in male S. romana to 115 in female S. sturanyi). The number of segments correlates with maximum body size. © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society, 2008, 153 , 253–286.     

Phylogeny and genus-level classification of mantellid frogs (Amphibia, Anura)

We propose a novel classification of frogs in the family Mantellidae, based on published phylogenetic information and on a new analysis of molecular data. Our molecular tree for 53 mantellid species is based on 2419 base pairs of the mitochondrial 12S rRNA, 16S rRNA, tRNAVal and cytochrome b genes, and of the nuclear rhodopsin gene. Because the genus Mantidactylus Boulenger sensu lato is confirmed to be paraphyletic with respect to Mantella Boulenger, and is highly diverse in morphology and reproductive biology, we propose to partition Mantidactylus into seven genera by elevating four subgenera to genus rank (Blommersia Dubois, Guibemantis Dubois, Spinomantis Dubois, and Gephyromantis Methuen) and creating two new genera (Boehmantis gen. n. and Wakea gen. n.). In addition, we create the new subgenera Boophis (Sahona) subgen. n., Gephyromantis (Duboimantis) subgen. n., G. (Vatomantis) subgen. n., and Mantidactylus (Maitsomantis) subgen. n. The following species are transferred to Spinomantis, based on their phylogenetic relationships: S. elegans (Guibé) comb. n. (formerly in Mantidactylus subgenus Guibemantis); S. bertini (Guibé) comb. n. and S. guibei (Blommers-Schlösser) comb. n. (both formerly in Mantidactylus subgenus Blommersia); S. microtis (Guibé) comb. n. (formerly in Boophis Tschudi). Within Boophis, the new B. mandraka species group and B. albipunctatus species group are established. Boophis rhodoscelis (Boulenger) is transferred to the B. microtympanum group. The following five species are revalidated: Mantidactylus bellyi Mocquard and M. bourgati Guibé (not junior synonyms of M. curtus (Boulenger)); M. cowanii (Boulenger) (not syn. M. lugubris (Duméril)); M. delormei Angel (not syn. M. brevipalmatus Ahl); Mantella ebenaui (Boettger) (not syn. M. betsileo (Grandidier)). The new classification accounts for recent progress in the understanding of the phylogeny and natural history of these frogs, but it is still tentative for a number of species. Future modifications may be necessary, especially as concerns species now included in Gephyromantis and Spinomantis.Full article published online at: http://www.senckenberg.de/odes/06-11.htm