208 research outputs found

    New genus and two new species of the Lower Cretaceous Digger Wasp from Spain (Hymenoptera: Sphecidae: Angarosphecinae)

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    One new genus and two new species, Ilerdosphex wenzae RASNITSYN n.gen. and n.sp. and Pompilopterus montsecensis RASNITSYN n.sp., are described in the digger wasp subfamily Angarosphecinae (Sphecidae) from the Lower Cretaceous (possibly Barremian) lithographic limestones of the La Pedrera de MeiĂ  fossil site in the Montsec Range, NE Spain

    Two new Lower Cretaceous hymenopterous insects (Insecta: Hymenoptera) from Sierra del Montsec, Spain

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    Two new hymenoterans are described from the Lower Barremian lithographic limestones of Sierra del Montsec (Lleida, Spain), Leridatoma pulcherrimapulcherima n.gen., n.sp. (Xyelotomidae RASNITSYN, 1968) that combines the most and the least advanced character states in the family (in structure of antenna and fore wing RS, respectively), and Cretephialtites pedrerae n.gen., n.sp. (Ephialtitidae HANDLIRSCH, 1906)

    Identity of Prosepididontus calpterys Handlirsch 1920 (Insecta: Grylloblattida: Geinitziidae)

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    Prosepididontus calopteryx HANDLIRSCH 1920, from the upper Lower Jurassic of Germ a ny, is transferred from Trichoptera to Grylloblattida: Geinitziidae. The anal loop like structure of Prosepididontus calopteryx is built of the concave CuP and two anal veins. Prosepididontidae HANDLIRSCH, 1920 is synonymised under Geinitziidae HANDLIRSCH, 1906.Prosepididontus calopteryx HANDLIRSCH 1920, from the upper Lower Jurassic of Germ a ny, is transferred from Trichoptera to Grylloblattida: Geinitziidae. The anal loop like structure of Prosepididontus calopteryx is built of the concave CuP and two anal veins. Prosepididontidae HANDLIRSCH, 1920 is synonymised under Geinitziidae HANDLIRSCH, 1906

    Wasps (Insecta: Vespida = Hymenoptera) from the Early Cretaceous of Spain

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    Wasps and their relatives from the Lower Cretaceous lithographic limestones of Spain have been studied. Thirty specimens representing 30 species (4 of them with undetermined placement), at least 21 genera and 11 families are recorded. We erect 1 new family - Andrenelidae-, 6 new genera and 11 new species: Meiaghilarella cretacica n.gen., n.sp. (Sepulcidae Ghilarellinae), Eosyntexis catalonicus n.sp., Cretosyntexis montsecensis n.gen., n.sp. (Anaxyelidae Syntexinae), Montsecephialtites zherikhini n.gen., n.sp. (Ephialtitidae Ephialtitinae), Karataus hispanicus n.sp. (Ephialtitidae Symphytopterinae), Manlaya ansorge i n.sp. (Gasteruptiidae Baissinae), Andrenelia pennata n.gen., n.sp. (Andrenelidae n. fam.), Cretoserphus gomezi n.gen., n.sp. (Mesoserphidae), Montsecosphex jarzembow skii n.gen., n.sp., Angarosphex penyalveri n.sp., Pompilopterus (?) noguerensis n.sp. (Sphecidae Angarosphecinae), Cretoscolia conquensis n.sp. (Scoliidae Archaeoscoliinae). The Mesozoic family Ephialtitidae is revisited based on the restudy of the type-species. We compare these Spanish Cretaceous assemblages with other ones from various parts of the world: Central and Eastern Asia, England, Australia, and Brazil. The number of genera and families identified in the Spanish fossil-sites is almost the same as in the English Purbeck and Wealden. The absence of some hymenopteran groups as Xyelidae, is consistent with the warm climate know to exist in Spain during the Early Cretaceous. We conclude that both La CabrĂșa and La Pedrera assemblages - the two sites that have yielded the greatest number of species- correspond to the Lower Cretaceous “Baissin type” (sensu Rasnitsyn et al., 1998), but including some Jurassic “survivors”. La Pedrera assemblage fits equally well in the “angarosphecine subtype”, while La CabrĂșa roughly corresponds to the “proctotrupid” one, although shows a comparative ly high proportion of angarosphecins. This fact may suggest: a) possibly asynchrony between these two fossilsites, b) environmental differences not reflected in the lithological record, c) different taphonomic processes and/or, d) insufficient sample size - to reflect the reality of the source populations-. La Pedrera assemblage is very similar to those from Weald Clay (England), Bon Tsagan (Mongolia) and Santana (Brazil). La CabrĂșa approaches to a some extent, though not quite agrees with the Purbeck (UK), Koonwarra (Australia), and most Lower Cretaceous Asian assemblages

    Cretobestiola, a replacement name for Bestiola Pulawski and Rasnitsyn, 1999 (Hymenoptera: Sphecidae)

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    We recently described a sphecid wasp genus Bestiola (in Rasnitsyn et al., 1999) to accommodate four species from Lower Cretaceous of Spain, eastern Russia, and Mongolia. This generic name, however, is preoccupied by Bestiola Nikol’skaya (1963), an aphelinid, as pointed to us by Mr. John K. Page (Zoological Records, York, Great Britain) and also by Signor Guido Pagliano (Torino, Italy). We therefore propose the name Cretobestiola to replace it. The name is derived from the Latin names creta (chalk), with reference to Cretaceous geological period, and bestiola (little beast).We recently described a sphecid wasp genus Bestiola (in Rasnitsyn et al., 1999) to accommodate four species from Lower Cretaceous of Spain, eastern Russia, and Mongolia. This generic name, however, is preoccupied by Bestiola Nikol’skaya (1963), an aphelinid, as pointed to us by Mr. John K. Page (Zoological Records, York, Great Britain) and also by Signor Guido Pagliano (Torino, Italy). We therefore propose the name Cretobestiola to replace it. The name is derived from the Latin names creta (chalk), with reference to Cretaceous geological period, and bestiola (little beast)

    Central nervous system and muscular bundles preserved in a 240 million year old giant bristletail (Archaeognatha: Machilidae)

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    Among the incomparably diverse group of insects no cases of central nervous system (CNS) preservation have been so far described in compression fossils. A third of the fossil insects collected from a 240-239 million year old (Ma) level at Monte San Giorgio UNESCO World Heritage (SwitzerlandItaly) underwent phosphatization, resulting in the extraordinary preservation of soft tissues. Here we describe Gigamachilis triassicus gen. et sp. nov. (Archaeognatha: Machiloidea: Machilidae) that, with an estimated total length of similar to 80 millimeters, represents the largest apterygote insect ever recorded. The holotype preserves: (i) components of the CNS represented by four abdominal ganglia, optic lobes with neuropils and compound retina;(ii) muscular bundles. Moreover, G. triassicus, possessing morphological features that prompt its assignment to the extant archaeognathan ingroup Machilidae, places the origin of modern lineages to Middle Triassic. Interestingly, at Monte San Giorgio, in the same stratigraphic unit the modern morphology of G. triassicus co-occurs with the ancient one represented by Dasyleptus triassicus (Archaeognatha: dagger Monura). Comparing these two types of body organization we provide a new reconstruction of the possible character evolution leading towards modern archaeognathan forms, suggesting the acquisition of novel features in a lineage of apterygote insects during the Permian or the Lower Triassic

    Hyptiogastrites electrinus Cockerell, 1917, from Myanmar (Burmese) amber: Redescription and its placement within the Evanioidea (Insecta: Hymenoptera)

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    © The Natural History MuseumThe wasp Hyptiogastrites electrinus Cockerell, 1917, from the Lower Cretaceous (Upper Albian) Myanmar (Burmese) amber is redescribed from the well-preserved holotype and its relationship with extant Aulacidae and Gasteruptiidae (Hymenoptera: Evanioidea) evaluated. Although the wing venation is identical to the majority of extant Hyptiogastrinae (Gasteruptiidae), phylogenetic analysis places H. electrinus as sister taxon to the Aulacidae s.str., (i.e. Aulacus + Pristaulacus). Thus, Hyptiogastrinae is confirmed as having a restricted Southern Hemisphere distribution (i.e. Australasia and South America). Consistent with this result, H. electrinus is included within a slightly more broadly defined Aulacidae rather than being placed in a new monotypic family. Characters that align this species with the Aulacidae include: having small circular eyes, percurrent Y-shaped notauli, pyramidal shape of the propodeum and the presence of a groove or ovipositor guide on the hind coxae.John T. Jennings, Andrew D. Austin and Nicholas B. Steven

    At last, a Pennsylvanian stem-stonefly (Plecoptera) discovered

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    <p>Abstract</p> <p>Background</p> <p>Stem-relatives of many winged insect orders have been identified among Pennsylvanian fossils (Carboniferous Period). Owing to their presumed 'basal' position in insect phylogeny, stoneflies were expected to occur at this period. However, no relative has ever been designated convincingly.</p> <p>Results</p> <p>In this paper, we report specimens belonging to a new fossil insect species collected from the Tupo Formation (Pennsylvanian; China). The wing venation of <it>Gulou carpenteri </it><b>gen. et sp. nov</b>. exhibits character states diagnostic of the order Plecoptera, but lack character states shared by unequivocal representatives of the order. Derived from this identification, the delimitation of the fossil species is ascertained based on comparison of several extant stonefly species. This comparative analysis allowed a trait present in <it>G. carpenteri </it><b>gen. et sp. nov</b>., but rarely occurring in extant species, to be documented and highlighted as atavistic. Affinities of taxa formerly proposed as putative stem-stoneflies are reconsidered in the light of the new discovery.</p> <p>Conclusions</p> <p><it>Gulou carpenteri </it><b>gen. et sp. nov</b>. is considered the only genuine Plecoptera reported from the Pennsylvanian. Continuing efforts on the systematics of Pennsylvanian winged insects indicate a fauna more diverse than previously appreciated. It suggests that insects already had a long, yet undocumented, history by this time.</p

    The taming of an impossible child: a standardized all-in approach to the phylogeny of Hymenoptera using public database sequences

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    <p>Abstract</p> <p>Background</p> <p>Enormous molecular sequence data have been accumulated over the past several years and are still exponentially growing with the use of faster and cheaper sequencing techniques. There is high and widespread interest in using these data for phylogenetic analyses. However, the amount of data that one can retrieve from public sequence repositories is virtually impossible to tame without dedicated software that automates processes. Here we present a novel bioinformatics pipeline for downloading, formatting, filtering and analyzing public sequence data deposited in GenBank. It combines some well-established programs with numerous newly developed software tools (available at <url>http://software.zfmk.de/</url>).</p> <p>Results</p> <p>We used the bioinformatics pipeline to investigate the phylogeny of the megadiverse insect order Hymenoptera (sawflies, bees, wasps and ants) by retrieving and processing more than 120,000 sequences and by selecting subsets under the criteria of compositional homogeneity and defined levels of density and overlap. Tree reconstruction was done with a partitioned maximum likelihood analysis from a supermatrix with more than 80,000 sites and more than 1,100 species. In the inferred tree, consistent with previous studies, "Symphyta" is paraphyletic. Within Apocrita, our analysis suggests a topology of Stephanoidea + (Ichneumonoidea + (Proctotrupomorpha + (Evanioidea + Aculeata))). Despite the huge amount of data, we identified several persistent problems in the Hymenoptera tree. Data coverage is still extremely low, and additional data have to be collected to reliably infer the phylogeny of Hymenoptera.</p> <p>Conclusions</p> <p>While we applied our bioinformatics pipeline to Hymenoptera, we designed the approach to be as general as possible. With this pipeline, it is possible to produce phylogenetic trees for any taxonomic group and to monitor new data and tree robustness in a taxon of interest. It therefore has great potential to meet the challenges of the phylogenomic era and to deepen our understanding of the tree of life.</p
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