Phylogeny and biogeography of Coenonympha butterflies (Nymphalidae: Satyrinae) – patterns of colonization in the Holarctic

Abstract We studied the historical biogeography of a group of butterflies in the Holarctic region belonging to the genus Coenonympha (Nymphalidae: Satyrinae: Coenonymphina), based on a phylogenetic hypothesis estimated from three genes. The genus is distributed mainly in the Palaearctic region, with two species extending into the Nearctic region. The tree is generally well supported and shows that Coenonympha is paraphyletic with respect to Lyela ( syn.n. ) and Triphysa ( syn.n. ), and we hence synonymize the latter two with Coenonympha. Within Coenonympha we identify three species groups, the tullia, glycerion and hero groups. The North American tullia exemplars are not sister to the Eurasian ones. A diva analysis indicates that the ancestor of the group was present in the Central Palaearctic or Central Palaeartic + Western Palaearctic or Central Palaearctic + Eastern Palaearctic. We conclude that the most likely origin of extant members of Coenonympha was in the Central Asian mountains. The tullia and hero groups started diverging in Europe following dispersal into the region. There have been two independent colonizations into Africa. The drying up of the Mediterranean during the Messinian period probably played an important role, allowing colonization into the Mediterranean islands and Africa.     

Phylogenetic revision of the North American Asidini (Coleoptera: Tenebrionidae)

The asidine darkling beetles (Coleoptera: Tenebrionidae: Asidini) are a morphologically diverse tribe of flightless tenebrionids found in many arid and sub‐arid habitats around the world. The 260 currently described North American species are contained in 27 genera, all of which are restricted to the western half of the continent. Evolutionary relationships within and between the North American Asidini (Coleoptera: Tenebrionidae) genera were reconstructed using partial sequences of mitochondrial cytochrome c oxidase I (COI) (660 bp) and nuclear ribosomal 28S (D2 region) (492 bp), and 100 phenotypic characters for 50 North American asidine species, representing 20 of the 27 currently described genera and 1 new genus. Species from two additional tenebrionid tribes (Branchini and Coniontini) and the South American asidine genus Cardigenius were chosen as outgroups. Analyses were performed using maximum parsimony and Bayesian inference methods. Clade support was inferred based on the posterior probability distribution of tree topologies, nonparametric bootstrap analysis, and partitioned Bremer support indices. The generic classification of the North American Asidini is revised based on the results, with ten genera recognized. Seven current genera: Craniotus LeConte, Heterasida Casey, Litasida Casey, Microschatia Solier, Pelecyphorus Solier, Philolithus Lacordaire, Stenomorpha Solier, are redescribed, and Ardamimicus Smith gen.n ., Ferveoventer Smith gen.n . and Micrasida Smith gen.n . are described, including Ardamimicus cognatoi Smith sp.n ., Ferveoventer browni Smith sp.n . and Micrasida obrienorum Smith sp.n . Twenty current genera are treated as subgenera pending further analyses: Philolithus Lacordaire with subgenera Glyptasida Casey, Gonasida Casey, Herthasida Wilke and Tisamenes Champion; Pelecyphorus Solier, with subgenera: Astrotus LeConte, Parasida Casey (= Plesiasida nom.n ), Poliorcetes Champion, Sicharbas Champion, Stenosides Solier, Ucalegon Champion and Zaleucus Champion, and Stenomorpha Solier with subgenera Asidina Casey, Asidopsis Casey, Bothrasida Casey, Megasida Casey, Notiasida Casey, Platasida Casey, Pycnomorpha Motschulsky, Stethasida Casey and Trichiasida Casey; all stat.rev .     

The three-dimensional structure of the central region in a synaptonemal complex: a comparison between rat and two insect species,Drosophila melanogaster andBlaps cribrosa

The highly ordered central region of the synaptonemal complex (SC) inBlaps cribrosa has recently been studied by electron microscope tomography (EMT), and a simple three-dimensional model presented. Using the same experimental approach we have now compared the central region inBlaps with the central regions inDrosophila melanogaster and rat. In all three species, the SCs exhibit a central element (CE) flanked by two lateral elements (LEs). The central region between the two LEs is crossed by transverse filaments (TFs). TheBlaps CE element is the most ordered one with a well-defined ladder-like structure with two longitudinal components bridged by a number of regularly spaced transverse components, the rungs of the ladder. At the junctions between the longitudinal and transverse components there are prominent dense structures. The CE is multi-layered with the ladders of the separate layers in approximate register. InDrosophila the transverse CE components are as distinct and well organized as inBlaps, while in rat they are present but are less frequent and less well ordered. The longitudinal CE components inDrosophila are often fragmented and even more so in rat. The tomographic analysis revealed that in all three species the central region contains the same structural units: a single TF associated with two short pillars (or globules), which correspond to the junction structures. A fibrous lattice connects the two pillars/globules on the same TF forming the transverse CE component and those on adjacent TFs forming the longitudinal CE component; fibers between pillars/globules also link consecutive CE layers together. In the longitudinal component the number of fibrous bridges between the pillars/globules is related to the conspicuousness of the longitudinal component, i.e.Blaps has most,Drosophila almost as many, and rat considerably fewer bridges. We conclude that the central region in rat,Drosophila andBlaps contains the same basic structural unit but the degree of order and concentration of the units differ: a higher density seems to be accompanied by a higher order within the CE.     

Rove beetles of the subtribe Scopaeina Mulsant & Rey (Coleoptera: Staphylinidae) in the West Palaearctic: Phylogeny, biogeography and species catalogue

A cladistic analysis of the West Palaearctic Scopaeina Mulsant & Rey, 1878 (Coleoptera, Staphylinidae: Paederinae) is presented along with bionomic and biogeographic information. A total of 76 morphological characters were coded for the 88 currently known West Palaearctic species, except for S. bifossicapitata (Outerelo & Oromi, 1987). Results show that Scopaeina comprises two well-supported monophyletic groups in the West Palaearctic, Micranops Cameron, 1913 and Scopaeus Erichson, 1840, which are considered to represent distinct genera. Phylogenetic relationships to Orus Casey, 1884, distributed in North and South America, are briefly discussed. Whereas Micranops is only represented by M. pilicornis (Baudi, 1869) in the region under study, 87 species of Scopaeus are currently known from the West Palaearctic. Within Scopaeus, the cladistic analysis yielded many well-supported monophyletic species groups, most of which are restricted to the West Palaearctic. However, except for Hyperscopaeus Coiffait, 1984, they are not in agreement with the widely used subgeneric concept sensu Coiffait (1952–1984). The following polyphyletic subgenera are consequently synonymized: Alloscopaeus Coiffait, 1968, Anomoscopaeus Coiffait, 1968, Geoscopaeus Coiffait, 1960, and Hyposcopaeus Coiffait, 1960 synn. n. = Scopaeus Erichson, 1840. Nivorus Herman, 1965, and Microscopaeus Coiffait, 1981 synn. n. = Micranops Cameron, 1913. The monotypical genus Coecoscopaeus Coiffait, 1984, established for C. coecus (Peyerimhoff, 1906), is excluded from Scopaeina. Scopaeus mitratus perroti Ochs, 1953 is raised to species rank, and S. nigellus Wollaston, 1864, formerly a synonym of S. minimus Erichson, 1939, is revalidated. Finally, we present a catalogue of species and synonyms of West Palaearctic Scopaeina along with distributional data and five new synonymies of species group names: S. bordei Peyerimhoff, 1914 syn. n. = S. portai Luze, 1910; S. tassiliensis Jarrige, 1958, S. mauretanicus Coiffait, 1960 synn. n. = S. crassipes Wollaston, 1867; S. saoudiensis Coiffait, 1981 = S. sinaicus Coiffait, 1970; S. mateui Coiffait, 1953 syn. n. = S. didymus Erichson, 1840. A lectotype is designated for S. didymus Erichson, 1840.See also Electronic Supplement (Parts 13) at http://www.senckenberg.de/odes/02-02.htm     

The genus Alphitobius Stephens (Coleoptera,Tenebrionidae, Alphitobiini) in Africa and adjacent islands

All species of the genus Alphitobius Stephens, 1829 (Alphitobiini Reitter, 1917, subfamily Tenebrioninae Latreille, 1802) from Africa and adjacent islands are revised. New species: Alphitobius capitaneus sp. n. from Kenya. New synonyms: Cryptops ulomoides Solier, 1851, syn. n. of Alphitobius diaperinus (Panzer, 1796); Alphitobius rufus Ardoin, 1976, syn. n. of Alphitobius hobohmi Koch, 1953); Peltoides (Micropeltoides) crypticoides Pic, 1916, syn. n. of Peltoides (Micropeltoides) opacus (Gerstaecker, 1871), comb. n. Homonym: Alphitobius ulomoides Koch, 1953 = Alphitobius arnoldi nom. n. New combinations from Alphitobius: Ulomoides basilewskyi (Ardoin, 1969), comb. n.; Peltoides (Micropeltoides) opacus (Gerstaecker, 1871), comb. n. Figures of all examined species are added and a species key is compiled.     

New and little known phalangopsinae (Orthoptera,Gryllidae): 7. Neotropical taxa of the tribes Paragryllini and Luzarini

Three new genera, one new subgenus, and 13 new species (Strogulomorpha separata sp. n., S. davidi sp. n., S. proxima sp. n., Luzarida lata sp. n., Luzara venado sp. n., L. sapani sp. n., Ucayacla pulchella gen. et sp. n., Peruzara atalaya gen. et sp. n., P. loreto sp. n., Amazonacla imitata gen. et sp. n., A. primitiva sp. n., Leptopsis (Leptopsis) ucayali sp. n., and L. (Aberracla subgen. n.) morona sp. n.) are described. The composition of the tribes Paragryllini and Luzarini and of the genera Luzarida Heb. and Luzara Walk is discussed. The new synonymies Luzarida Hebard, 1928 = Ecuazarida Nischk et Otte, 2000, syn. n.; Lerneca Walker, 1869 = Doposia Otte et Perez-Gelabert, 2009, syn. n.; Nemoricantor Desutter-Grandcolas et Hubbell, 1993 = Kumalorina Otte et Perez-Gelabert, 2009, syn. n. are given. The systematic position of some previously described species is corrected.     

Towards a revision of the South American genus Praocis Eschscholtz (Coleoptera,Tenebrionidae), with estimation of the diversity of each subgenus

A review of the subgenera of the South American genus Praocis Eschscholtz (Pimeliinae: Praociini) is presented. Praocis comprises 77 species and 8 subspecies arranged in nine subgenera distributed in arid lands from Central Peru and Bolivia to the Southern part of Patagonia in Chile and Argentina. For each subgenus of Praocis: Praocis Eschscholtz, Mesopraocis Flores & Pizarro-Araya, subgen. n., Anthrasomus Guérin-Méneville, Filotarsus Gay & Solier, Postpraocis Flores & Pizarro-Araya, subgen. n., Hemipraocis Flores & Pizarro-Araya, subgen. n., Orthogonoderes Gay & Solier, Praonoda Flores & Pizarro-Araya, subgen. n., and Praocida Flores & Pizarro-Araya, subgen. n., we present a diagnosis using new and constant characters of adult morphology such as clypeal configuration, length and proportion of antennomeres 9, 10 and 11, arrangement of apical tomentose sensory patches on antennomeres 10 and 11, anterior margin of prosternum, lateral margin of elytron, ventral surface of profemora, and shape of protibiae. An identification key for the nine subgenera of Praocis is presented. Type species are designated for the five new subgenera; for Mesopraocis: Praocis calderana Kulzer, for Postpraocis: Praocis pentachorda Burmeister, for Hemipraocis: Praocis sellata Berg, for Praonoda: Praocis bicarinata Burmeister, for Praocida: Praocis zischkai Kulzer, and for the previously described subgenus Orthogonoderes: Praocis subreticulata Gay & Solier. The current number of species and the estimated number of species to be described are presented. The distribution ranges of the subgenera, including new records from collections and recent expeditions, are given. Habitat preferences and a discussion of the biogeography of the genus are also presented.     

Geometric morphometric analysis of a new Miocene bumble bee from the Randeck Maar of southwestern Germany (Hymenoptera: Apidae)

The first fossil bumble bee (Apinae: Bombini) from the Miocene Randeck Maar of southwestern Germany is described and illustrated. The specimen is subjected to a geometric morphometric analysis along with a diversity of other bumble bee species representing most major extant lineages, and particularly the subgenus Bombus s.s. The morphometric analysis supports the placement of the Randeck Maar species within Bombus s.s., as a species distinct from all others in the subgenus. It shows that extant subgenera of bumblebees were already derived in the early/middle Miocene. The Randeck Maar fossil is formally described as Bombus (Bombus) randeckensis Wappler & Engel sp. n. .     

Minute moss beetles in the Southern Hemisphere: Molecular phylogeny,historical biogeography and habitat shifts (Coleoptera: Hydraenidae)

Minute moss beetles (Hydraenidae) are one of the most speciose and widespread families of aquatic Coleoptera, with an estimated 4000 extant species, found in the majority of aquatic habitats from coastal rock pools to mountain streams and from the Arctic Circle to the Antarctic islands. Molecular phylogenetic works have improved our understanding of the evolutionary history of the megadiverse Hydraena, Limnebius and Ochthebius in recent years, but most genera in the family have not yet been included in any phylogenetic analyses, particularly most of those which are restricted to the Southern Hemisphere. Using a multimarker molecular matrix, sampling over 40% of described species richness and 75% of currently recognized genera, we infer a comprehensive molecular phylogeny of these predominantly Gondwanan Hydraenidae. Whilst the genera we focus on are morphologically diverse, and currently classified across all four hydraenid subfamilies, our phylogenetic analyses suggest that these Gondwanan genera may instead constitute a single clade. As a result of our findings, the African genus Oomtelecopon Perkins syn.n. is shown to nest within Coelometopon Janssens, the New Zealand Homalaena Ordish syn.n. and Podaena Ordish syn.n. are synonymised with Orchymontia Broun, and the South African Pterosthetops Perkins syn.n. is synonymised with Prosthetops Waterhouse, resulting in Pterosthetopini Perkins syn.n. being synonymised with Prosthetopini Perkins. Mesoceratops Bilton & Jäch gen.n. is erected to accommodate six former members of Mesoceration Janssens, which is shown to be polyphyletic. We propose the replacement name Orchymontia ordishi Jäch & Bilton nom.n. for Homalaena dilatata Ordish, 1984 (now a junior homonym); altogether 39 new combinations are proposed. Our Bayesian divergence times infer an origin for this ‘Gondwana group’ of genera in Africa plus Madagascar in the mid-Cretaceous and suggest that both vicariant and dispersal processes, together with extinctions, have shaped the biogeographic history of these beetles in the Southern Hemisphere during the Cretaceous, resulting in geographically conserved extant lineages. Finally, we reconstruct ancestral habitat shifts across our phylogeny, revealing numerous changes in habitat occupancy in these genera, including multiple origins of fully terrestrial, humicolous taxa in different regions.     

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).     

Pupae in nomenclature and identification: West Palaearctic Orthocladius s.str. (Diptera: Chironomidae) revised

Abstract. Orthocladius (Orthocladius) is a subgenus of one of the more speciose genera amongst the Holarctic chironomids of the subfamily Orthocladiinae. Although many names have been applied, adult males are difficult to distinguish. However, the immature stages often are known, and pupae discriminate taxa reliably. Based predominantly upon examination of exuviae, Orthocladius atripluma Kieffer and Orthocladius mitisi Goetghebuer are syn.n . of Orthocladius glabripennis (Goetghebuer); Orthocladius smolandicus Brundin a syn.n . of Orthocladius holsatus Goetghebuer; Orthocladius lenzi Kieffer a syn.n . of Orthocladius oblidens (Walker); Orthocladius rhyacobius Kieffer, Orthocladius rhyacophilus Kieffer and Orthocladius excavatus Brundin are syn.n . of Orthocladius obumbratus Johannsen; Orthocladius saxicola Kieffer and Orthocladius curtiseta Sæther are syn.n . of Orthocladius rubicundus (Meigen). Orthocladius (Orthocladius) vaillanti is described as sp.n ., based upon distinctive pupal exuviae. Lectotypes are designated for Orthocladius rhyacobius Kieffer, Orthocladius rhyacophilus Kieffer, Orthocladius rivinus Kieffer, Chironomus rubicundus Meigen and Orthocladius saxicola Kieffer. A key to the thirteen western palaearctic species is given.     

Ancient DNA from an extinct Mediterranean micromammal—Hypnomys morpheus (Rodentia: Gliridae)—Provides insight into the biogeographic history of insular dormice

The dormice (Gliridae) are a family of rodents represented by relatively few extant species, though the family was much more species-rich during the Early Miocene. Intergeneric phylogenetic relationships among glirids in some cases remain unresolved, despite extensive molecular and morphological analyses. Uncertainty is greatest with respect to the relationships among fossil taxa and how extinct lineages are related to modern species. The fossil genus Hypnomys from the Balearic Islands (western Mediterranean Sea) includes the Late Pleistocene–Holocene species Hypnomys morpheus, which has variously been considered a close relative or subgenus of the extant Eliomys. In the present study, we sequenced ancient mitochondrial DNA from H. morpheus, which suggests a sister relationship with the extant members of Eliomys. In addition, the pairwise sequence variation between Hypnomys and Eliomys is higher than that observed between congeneric glirid species (e.g., many Graphiurus spp.), which allows us to reject the hypothesis that Hypnomys is a subgenus of Eliomys. Our molecular dating analyses suggest that Hypnomys and Eliomys diverged 13.67 million years ago (95% highest posterior density [HPD] = 7.39–20.07). The relatively early split between these genera together with the molar morphology of early representatives of Hypnomys points to a Middle-Late Miocene origin from a continental glirid with a complex molar pattern, such as Vasseuromys or a closely related genus.     

The evolution of myrmicine ants: phylogeny and biogeography of a hyperdiverse ant clade (Hymenoptera: Formicidae)

This study investigates the evolutionary history of a hyperdiverse clade, the ant subfamily Myrmicinae (Hymenoptera: Formicidae), based on analyses of a data matrix comprising 251 species and 11 nuclear gene fragments. Under both maximum likelihood and Bayesian methods of inference, we recover a robust phylogeny that reveals six major clades of Myrmicinae, here treated as newly defined tribes and occurring as a pectinate series: Myrmicini, Pogonomyrmecini trib.n. , Stenammini, Solenopsidini, Attini and Crematogastrini. Because we condense the former 25 myrmicine tribes into a new six‐tribe scheme, membership in some tribes is now notably different, especially regarding Attini. We demonstrate that the monotypic genus Ankylomyrma is neither in the Myrmicinae nor even a member of the more inclusive formicoid clade—rather it is a poneroid ant, sister to the genus Tatuidris (Agroecomyrmecinae). Several species‐rich myrmicine genera are shown to be nonmonophyletic, including Pogonomyrmex, Aphaenogaster, Messor, Monomorium, Pheidole, Temnothorax and Tetramorium. We propose a number of generic synonymies to partially alleviate these problems (senior synonym listed first): Pheidole = Anisopheidole syn.n. = Machomyrma syn.n. ; Temnothorax = Chalepoxenus syn.n. = Myrmoxenus syn.n. = Protomognathus syn.n. ; Tetramorium = Rhoptromyrmex syn.n. = Anergates syn.n. = Teleutomyrmex syn.n. The genus Veromessor stat.r. is resurrected for the New World species previously placed in Messor; Syllophopsis stat.r. is resurrected from synonymy under Monomorium to contain the species in the hildebrandti group; Trichomyrmex stat.r. is resurrected from synonymy under Monomorium to contain the species in the scabriceps‐ and destructor‐groups; and the monotypic genus Epelysidris stat.r. is reinstated for Monomorium brocha. Bayesian divergence dating indicates that the crown group Myrmicinae originated about 98.6 Ma (95% highest probability density 87.9–109.6 Ma) but the six major clades are considerably younger, with age estimates ranging from 52.3 to 71.1 Ma. Although these and other suprageneric taxa arose mostly in the middle Eocene or earlier, a number of prominent, species‐rich genera, such as Pheidole, Cephalotes, Strumigenys, Crematogaster and Tetramorium, have estimated crown group origins in the late Eocene or Oligocene. Most myrmicine species diversity resides in the two sister clades, Attini and Crematogastrini, which are estimated to have originated and diversified extensively in the Neotropics and Paleotropics, respectively. The newly circumscribed Myrmicini is Holarctic in distribution, and ancestral range estimation suggests a Nearctic origin. The Pogonomyrmecini and Solenopsidini are reconstructed as being Neotropical in origin, but they have subsequently colonized the Nearctic region (Pogonomyrmecini) and many parts of the Old World as well as the Nearctic region (Solenopsidini), respectively. The Stenammini have flourished primarily in the northern hemisphere, and are most likely of Nearctic origin, but selected lineages have dispersed to the northern Neotropics and the Paleotropics. Thus the evolutionary history of the Myrmicinae has played out on a global stage over the last 100 Ma, with no single region being the principal generator of species diversity. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub: BB6829C4‐DA79‐45FE‐979E‐9749E237590E .     

The Neotropical genus Anaisus (Elateridae) and its relationship to the Pyrophorinae

Four species of the genus Anaissus Candeze are recognized and described or redescribed and a key for their identification is given; anandra sp.n., aurantium spn., fuscipes sp.n. and tarsalis Candeze (=spinipennis syn.n.). A new subgenus Auctumnalis is erected with aurantium as type-species. Two possible species from Brazil and French Guiana respectively are also reported. The systematic position of the genus is discussed in relation to the Neotropical Pyrophorinae, and on the basis of adult characters Anaissus is here assigned to the subfamily Pyrophorinae.     

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     

Two new species of the genus Philaenus (Homoptera, Aphrophoridae) from Iran

Two new species of Philaenus from Iran are described. Philaenus elbursianus sp. n. belongs to the Ph. signatus species group from the nominotypical subgenus. Philaenus iranicus sp. n. differs considerably from all the known representatives of the genus and was separated in a new subgenus Gyrurus subgen. n. The occurrence of this highly peculiar species in Iran may indicate that the center of origin of the genus Philaenus lies in this territory and not in the Mediterranean region as it was considered before.     

Revision of the Eastern Asian genera Ambrostoma Motschulsky and Parambrostoma Chen (Coleoptera: Chrysomelidae: Chrysomelinae)

The leaf beetle genera Ambrostoma Motschulsky, 1860 and Parambrostoma Chen, 1934 have been revised and now include 14 species. Two new species from Nepal are described, Parambrostoma kippenbergi sp.n. and P. medvedevi sp.n. Three new synonymies are established: Ambrostoma rugosopunctatum Chen = Ambrostoma (Parambrostoma) laosensis Kimoto & Gressitt, syn.n. , Ambrostoma rugosopunctatum Chen = Ambrostoma daccordii Medvedev, syn.n., Ambrostoma fortunei (Baly) = Ambrostoma quadriimpressum chusanica Gruev, syn.n . One species was transferred from Chrysomela Linnaeus to Ambrostoma Motschulsky: A. superbum (Thunberg), comb.n . All the species now included are described and illustrated. Microcomputer tomography was applied for the first time in a study on chrysomelid beetles. A cladistic analysis based on morphological characters of adults was conducted to reconstruct the intergeneric and interspecific phylogeny of Ambrostoma and Parambrostoma. The results show that the monophyly of both genera is well supported. Ambrostoma is widespread in East Asia, whereas Parambrostoma is restricted to the southern slope of the Himalayas, where a relatively recent and modest speciation took place.     

CAESALPINIA SUBGENUS MEZONEURON (LEGUMINOSAE,CAESALPINIOIDEAE) FROM THE TERTIARY OF NORTH AMERICA

Legume fruits from the Eocene of Tennessee and Wyoming and the Miocene of Idaho are described and assigned to Caesalpinia subgenus Mezoneuron (Caesalpinioideae), an extant Paleotropical taxon that does not occur in North or South America today. Morphological and anatomical details of the fruits are used in evaluating their systematic relationships. The features of the fossil fruits are accommodated only within this extant subgenus. These fossils represent the only reliable known occurrence of C. subgenus Mezoneuron in the paleobotanical record. These fossils suggest that subgenus Mezoneuron was distinct from subgenus Caesalpinia by the Middle Eocene. Further, they document the widespread occurrence of this currently Paleotropical group for at least 30 million years in North America.     

A taxonomic revision of Labiostrongylus (Labiostrongylus) (Yorke & Maplestone, 1926) and Labiostrongylus (Labiomultiplex) n. subg. (Nematoda: Cloacinidae) from macropodid and potoroid marsupials

The morphological characters used to differentiate species in the genus Labiostrongylus Yorke & Maplestone, 1926, parasitic in macropodid and potoroid marsupials, are discussed. The genus is divided into three subgenera Labiostrongylus (Labiostrongylus), L. (Labiomultiplex) n. subg. and L. (Labiosimplex) n. subg. on the basis of the presence or absence of interlabia and the morphology of the oesophagus. A key to the subgenera is given and a detailed revision of two of the subgenera is presented. Keys to each of the subgenera are given, the species discussed being: L. (L.) labiostrongylus) (type-species) (syn. L. (L.) insularis, L. (L.) grandis, L. (L.) macropodis sp. inq. and L. (L.) nabarlekensis n. sp., in the subgenus Labiostrongylus, and L. (Lm.) eugenii, L. (Lm.) novaeguineae, L. (Lm.) onychogale, L. (Lm.) uncinatus, L. (Lm.) billardierii n. sp., L. (Lm.) constrictis n. sp., L. (Lm.) kimberleyensis n. sp., L. (Lm.) thylogale n. sp., and L. (Lm.) potoroi, n. sp., in the subgenus Labiomultiplex.