Hymenoptera: Vespidae) in Newfoundland Barry Hicks
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An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
© Copyright Australian Museum, 2005 Records of the Australian Museum (2005) Vol. 57: 375–446. ISSN 0067-1975 An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna M.S. MOULDS Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] ABSTRACT. The history of cicada family classification is reviewed and the current status of all previously proposed families and subfamilies summarized. All tribal rankings associated with the Australian fauna are similarly documented. A cladistic analysis of generic relationships has been used to test the validity of currently held views on family and subfamily groupings. The analysis has been based upon an exhaustive study of nymphal and adult morphology, including both external and internal adult structures, and the first comparative study of male and female internal reproductive systems is included. Only two families are justified, the Tettigarctidae and Cicadidae. The latter are here considered to comprise three subfamilies, the Cicadinae, Cicadettinae n.stat. (= Tibicininae auct.) and the Tettigadinae (encompassing the Tibicinini, Platypediidae and Tettigadidae). Of particular note is the transfer of Tibicina Amyot, the type genus of the subfamily Tibicininae, to the subfamily Tettigadinae. The subfamily Plautillinae (containing only the genus Plautilla) is now placed at tribal rank within the Cicadinae. The subtribe Ydiellaria is raised to tribal rank. The American genus Magicicada Davis, previously of the tribe Tibicinini, now falls within the Taphurini. Three new tribes are recognized within the Australian fauna, the Tamasini n.tribe to accommodate Tamasa Distant and Parnkalla Distant, Jassopsaltriini n.tribe to accommodate Jassopsaltria Ashton and Burbungini n.tribe to accommodate Burbunga Distant. -
Cicadidae (Hemiptera Homoptera Auchenorrhyncha) (')
PARC NATIONAL DE L'UPEMBA NATIONAAL UPEMBA PARK I. MISSION G. F. DE WITTE I. ZENDING G. F. DE WITTE en collaboration avec met medewerking van W. ADAM. A. JANSSENS, L. VAN MEEL W. ADAM. A. JANSSENS, L. VAN MEEL et R. VERHEYEN (1946-1949). en R. VERHEYEN (1946-1949). Fascicule 59 (2) Aflevering 59 (2) CICADIDAE (HEMIPTERA HOMOPTERA AUCHENORRHYNCHA) (') BY Jiri DLABOLA (Praha) INTRODUCTION This is a continuation of my previous research work in the family Cicadidae, based partly upon the material belonging to the « Institut des Parcs Nationaux du Congo Belge, Bruxelles >>, partly on the material of the « Musée Royal du Congo Belge, Tervueren ». Taxonomy in Ethiopian Cicadas worked out already by Karsch, 1890, who keyed, described ancl partly made drawings of a number of the species from that continent, but when studying this classical literature we see that we can détermine comparatively easily some Cicadinne only, but not so many Tibiceninae, where even the séparation of genera is rather difficult. In this subfamily we cannot make any détermination at ail without seeing the type-specimens, excepting only some well marked or monotypic genera. But these déterminations on the basis of the available literature, even willi the help of the original descriptions, are rather problematical. Also the fact of the great dispersion of types in the European museums not accessible for everyone's study, forms the big generally known obstacle in cicadological taxonomie work. There remains here another question, i.e. whether the comparison of types can be satisfactory in every case, e.g. in such a genus as Trismarcha aso., where different sexes have served in single specimens t1) Second contribution to the Knowledge of the Cidadidae from the Belgian Congo. -
WORLD LIST of EDIBLE INSECTS 2015 (Yde Jongema) WAGENINGEN UNIVERSITY PAGE 1
WORLD LIST OF EDIBLE INSECTS 2015 (Yde Jongema) WAGENINGEN UNIVERSITY PAGE 1 Genus Species Family Order Common names Faunar Distribution & References Remarks life Epeira syn nigra Vinson Nephilidae Araneae Afregion Madagascar (Decary, 1937) Nephilia inaurata stages (Walck.) Nephila inaurata (Walckenaer) Nephilidae Araneae Afr Madagascar (Decary, 1937) Epeira nigra Vinson syn Nephila madagscariensis Vinson Nephilidae Araneae Afr Madagascar (Decary, 1937) Araneae gen. Araneae Afr South Africa Gambia (Bodenheimer 1951) Bostrichidae gen. Bostrichidae Col Afr Congo (DeFoliart 2002) larva Chrysobothris fatalis Harold Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) larva Lampetis wellmani (Kerremans) Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) syn Psiloptera larva wellmani Lampetis sp. Buprestidae Col jewel beetle Afr Togo (Tchibozo 2015) as Psiloptera in Tchibozo but this is Neotropical Psiloptera syn wellmani Kerremans Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) Psiloptera is larva Neotropicalsee Lampetis wellmani (Kerremans) Steraspis amplipennis (Fahr.) Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) larva Sternocera castanea (Olivier) Buprestidae Col jewel beetle Afr Benin (Riggi et al 2013) Burkina Faso (Tchinbozo 2015) Sternocera feldspathica White Buprestidae Col jewel beetle Afr Angola (DeFoliart 2002) adult Sternocera funebris Boheman syn Buprestidae Col jewel beetle Afr Zimbabwe (Chavanduka, 1976; Gelfand, 1971) see S. orissa adult Sternocera interrupta (Olivier) Buprestidae Col jewel beetle Afr Benin (Riggi et al 2013) Cameroun (Seignobos et al., 1996) Burkina Faso (Tchimbozo 2015) Sternocera orissa Buquet Buprestidae Col jewel beetle Afr Botswana (Nonaka, 1996), South Africa (Bodenheimer, 1951; syn S. funebris adult Quin, 1959), Zimbabwe (Chavanduka, 1976; Gelfand, 1971; Dube et al 2013) Scarites sp. Carabidae Col ground beetle Afr Angola (Bergier, 1941), Madagascar (Decary, 1937) larva Acanthophorus confinis Laporte de Cast. -
Checklist of the Scale Insects (Hemiptera : Sternorrhyncha : Coccomorpha) of New Caledonia
Checklist of the scale insects (Hemiptera: Sternorrhyncha: Coccomorpha) of New Caledonia Christian MILLE Institut agronomique néo-calédonien, IAC, Axe 1, Station de Recherches fruitières de Pocquereux, Laboratoire d’Entomologie appliquée, BP 32, 98880 La Foa (New Caledonia) [email protected] Rosa C. HENDERSON† Landcare Research, Private Bag 92170 Auckland Mail Centre, Auckland 1142 (New Zealand) Sylvie CAZÈRES Institut agronomique néo-calédonien, IAC, Axe 1, Station de Recherches fruitières de Pocquereux, Laboratoire d’Entomologie appliquée, BP 32, 98880 La Foa (New Caledonia) [email protected] Hervé JOURDAN Institut méditerranéen de Biodiversité et d’Écologie marine et continentale (IMBE), Aix-Marseille Université, UMR CNRS IRD Université d’Avignon, UMR 237 IRD, Centre IRD Nouméa, BP A5, 98848 Nouméa cedex (New Caledonia) [email protected] Published on 24 June 2016 Rosa Henderson† left us unexpectedly on 13th December 2012. Rosa made all our recent c occoid identifications and trained one of us (SC) in Hemiptera Sternorrhyncha slide preparation and identification. The idea of publishing this article was largely hers. Thus we dedicate this article to our late and dear Rosa. Rosa Henderson† nous a quittés prématurément le 13 décembre 2012. Rosa avait réalisé toutes les récentes identifications de cochenilles et avait formé l’une d’entre nous (SC) à la préparation des Hemiptères Sternorrhynques entre lame et lamelle. Grâce à elle, l’idée de publier cet article a pu se concrétiser. Nous dédicaçons cet article à notre chère et regrettée Rosa. urn:lsid:zoobank.org:pub:90DC5B79-725D-46E2-B31E-4DBC65BCD01F Mille C., Henderson R. C.†, Cazères S. & Jourdan H. 2016. — Checklist of the scale insects (Hemiptera: Sternorrhyncha: Coccomorpha) of New Caledonia. -
ABSTRACTS Edited by Paul C
ABSTRACTS Edited by Paul C. Nascimbene 8th International Conference on Fossil Insects, Arthropods & Amber | Edited by Paul C. Nascimbene 1 8th International conference on fossil insects, arthropods and amber. Santo Domingo 2019 Abstracts Book ISBN 978-9945-9194-0-0 Edited by Paul C. Nascimbene Amber World Museum Fundación para el Desarrollo de la Artesanía International Palaeoentomological society Available at www.amberworldmuseum.com Contents Abstracts organized alphabetically by author (* denotes the presenter) IPS President’s Address Pages 3-5 Keynote Presentations Pages 6-15 Talks Pages 16-100 Posters Pages 101-138 8th International Conference on Fossil Insects, Arthropods & Amber | Edited by Paul C. Nascimbene 1 IPS President’s Address 2 8th International Conference on Fossil Insects, Arthropods & Amber | Edited by Paul C. Nascimbene “Palaeoentomology”: An advanced traditional science dealing with the past with modern technologies Dany Azar: President of the International Palaeoentomological Society *Lebanese University, Faculty of Science II, Fanar, Natural Sciences Department, Fanar - El- Matn, PO box 26110217, Lebanon. Palaeoentomology began formally in the late XVIIIth Century with publications on fossil insects in amber. At the start of the XIXth Century, the first studies and descriptions of insects from sedimentary rocks appeared. This discipline then developed during the XIXth and beginning of the XXth centuries, and resulted in major works and reviews. The end of the XXth and the beginning of XXIst centuries (especially after the famous film “Jurassic Park,” produced by Steven Spielberg in 1993 and based on the eponymous novel of Michael Crichton, together with the discovery of new rock and amber outcrops with fossil insects of different geological ages in various parts of the world), witnessed a significant and exponential growth of the science of palaeoentomology resulting in a huge amount of high- quality international scientific work, using the most advanced analytical, phylogenetic and imaging techniques. -
Historical Biogeography of the Tribe Platypleurini
HISTORICAL BIOGEOGRAPHY OF THE TRIBE PLATYPLEURINI SCHMIDT, 1918 (HEMIPTERA: CICADIDAE) WITH A FOCUS ON SOUTHERN AFRICA A thesis submitted in fulfilment of the requirements for the degree of DOCTOR OF PHILOSOPHY at RHODES UNIVERSITY by Benjamin Wills Price January 2010 Abstract Abstract With our contemporary biota under increasing threat of extinction, it is of interest to understand where, why and how biological diversity is generated. If focussed on appropriate taxa, phylogeographic and phylogenetic studies can assist in the identification of both places and processes central to the origin and maintenance of biological diversity. It is explained why southern Africa presents a perfect test-bed for exploring such mechanisms of diversification and why cicadas (Hemiptera: Cicadidae) have proved very suitable tools for studies of historical biogeography. This study then exemplifies these points by providing the first large-scale investigation of the historical biogeography of the tribe Platypleurini Schmidt, 1918, with emphasis on the genus Platypleura Amyot & Seville, 1843 in southern Africa. Standard methods of DNA sequencing provided data from portions of the mitochondrial small subunit ribosomal 16S RNA (16S) and cytochrome oxidase subunits I (COI) and II (COII); and the nuclear elongation factor 1 alpha (EF-1α) from 400 ethanol-preserved specimens. These data were analysed using standard phylogenetic methods and a time scale of diversification was estimated using a Bayesian framework and both fossil data and DNA substitution rates. The results showed that the tribe is too recent to be of Gondwanan origin. The lack of monophyly of the genera represented in both Asia and Africa showed that the tribe needs formal taxonomic revision. -
Insects As Food in Sub-Saharan Africa
Insect Sci. Applic. Vol. 23, No. 3, pp. 163–185,Insects 2003 as food in Africa 0191-9040/03 $3.00 + 0.00 163 Printed in Kenya. All rights reserved © 2003 ICIPE REVIEW ARTICLE INSECTS AS FOOD IN SUB-SAHARAN AFRICA A. VAN HUIS Laboratory of Entomology, Wageningen University, P.O. Box 8031, 6700 EH Wageningen, the Netherlands. E-mail: [email protected] (Accepted 14 August 2003) Abstract—Data on insects as food in sub-Saharan Africa were collected by reviewing the literature and conducting interviews in a number of African countries. A list of about 250 edible insect species from Africa was compiled. Of these, 78 percent are Lepidoptera (30%), Orthoptera (29%) and Coleoptera (19%), and 22 percent Isoptera, Homoptera, Hymenoptera, Heteroptera, Diptera and Odonota. Insects are rich in protein, vitamins and minerals, and a good source of iron and B-vitamins. Examples of insects being toxic are given, but often traditional methods are used to remove the poison. Whether or not insects are eaten depends not only on taste and nutritional value, but also on customs, ethnic preferences or prohibitions. The harvesting of insects is often done by women. The way of collecting depends on insects’ behaviour. For example, inactivity at low temperatures enables easy catching of locusts and grasshoppers in the morning. Night flyers (termites, some grasshoppers) can be lured into traps by light and some insects like palm weevils can be attracted to artificially created breeding sites. Some species (crickets, cicadas) can be located by the sound they make. A number of tools are used to facilitate capturing such as glue, sticks, nets and baskets. -
The Phylogeny and Evolution of Ants
ES45CH02-Ward ARI 15 October 2014 8:51 The Phylogeny and Evolution of Ants Philip S. Ward Department of Entomology & Nematology, and Center for Population Biology, University of California, Davis, California 95616; email: [email protected] Annu. Rev. Ecol. Evol. Syst. 2014. 45:23–43 Keywords First published online as a Review in Advance on Formicidae, fossil record, long-branch attraction, process heterogeneity, August 15, 2014 convergence, divergence The Annual Review of Ecology, Evolution, and Systematics is online at ecolsys.annualreviews.org Abstract This article’s doi: Originating most likely in the early Cretaceous, ants have diversified to be- 10.1146/annurev-ecolsys-120213-091824 come the world’s most successful eusocial insects, occupying most terrestrial Copyright c 2014 by Annual Reviews. ecosystems and acquiring a global ecological footprint. Recent advances in All rights reserved Annu. Rev. Ecol. Evol. Syst. 2014.45:23-43. Downloaded from www.annualreviews.org Access provided by University of California - Davis on 11/25/14. For personal use only. our understanding of ant evolutionary history have been propelled by the use of molecular phylogenetic methods, in conjunction with a rich (and still growing) fossil record. Most extant ants belong to the formicoid clade, which contains ∼90% of described species and has produced the most so- cially advanced and dominant forms. The remaining ants are old lineages of predominantly cryptobiotic species whose relationships to one another and to the formicoids remain unclear. Rooting the ant tree is challenging because of (a) a long branch separating ants from their nearest outgroup, and (b) heterogeneity in evolutionary rates and base composition among ant lineages. -
3 General Features of Insect History
3 General Features of Insect History 3.1 respectively, events that are hardly possible to be dated precisely). Indeed, the constant number of taxa recorded in two succeeding time Dynamics of Insect Taxonomic intervals may be due to the absence of any change, or may be due to high Diversity but equal numbers of taxic origins and extinctions (equal taxic birth and death rates). V.YU. DMITRIEV AND A.G. PONOMARENKO Because of these and related problems discussed at length by ALEKSEEV et al. (2001), a few relatively safe and informative methods have been selected. One of them is the momentary (= instantaneous) diversity on the boundary of two adjacent stratigraphic units which is The study of past dynamics of the taxonomic diversity is a complicated calculated as the number of taxa crossing the boundary (recorded both job, threatened by numerous traps and caveats connected mostly with above and below it). This permits us to avoid or minimise the errors improper or insufficiently representative material and inappropriate cal- caused by the unequal duration of the stratigraphic units, as well as by culating methods (ALEKSEEV et al. 2001). It is self-evident that the taxa irregular distribution of the exceptionally rich fossil sites that fill the used as operational units in the diversity calculation should be long liv- fossil record with numerous short lived taxa, a kind of noise in ing enough to have their duration at least roughly recordable in the fossil diversity dynamics research. record available, and yet not too long living to display their appreciable Instantaneous diversity can be plotted against the time scale turnover. -
A Dated Molecular Phylogeny of the Cicada Tribe Platypleurini Schmidt
Systematic Entomology (2019), DOI: 10.1111/syen.12360 Out of Africa? A dated molecular phylogeny of the cicada tribe Platypleurini Schmidt (Hemiptera: Cicadidae), with a focus on African genera and the genus Platypleura Amyot & Audinet-Serville BENJAMIN W. PRICE1 , DAVID C. MARSHALL2, NIGEL P. BARKER3, CHRIS SIMON2 andMARTIN H. VILLET4 1Life Sciences Department, Natural History Museum, London, U.K., 2Department of Ecology & Evolutionary Biology, University of Connecticut, Storrs, CT, U.S.A., 3Faculty of Natural & Agricultural Sciences, University of Pretoria, Hatfield, South Africa and 4Department of Zoology & Entomology, Rhodes University, Grahamstown, South Africa Abstract. The Platypleurini is a large group of charismatic cicadas distributed from Cape Agulhas in South Africa, through tropical Africa, Madagascar, India and eastern Asia to Japan, with generic diversity concentrated in equatorial and southern Africa. This distribution suggests the possibility of a Gondwanan origin and dispersal to eastern Asia from Africa or India. We used a four-gene (three mitochondrial) molecular dataset, fossil calibrations and molecular clock information to explore the phylogenetic relationships of the platypleurine cicadas and the timing and geography of their diversification. The earliest splits in the tribe were found to separate forest genera in Madagascar and equatorial Africa from the main radiation, and all of the Asian/Indian species sampled formed a younger clade nested well within the African taxa. The tribe appears to have diversified during the Cenozoic, beginning c. 50–32 Ma, with most extant African lineages originating in the Miocene or later, well after the breakup of the Gondwanan landmass. Biogeographical analysis suggests an African origin for the tribe and a single dispersal event founding the Asian platypleurines, although additional taxon sampling and genetic data will be needed to confirm this pattern because key nodes in the tree are still weakly supported. -
A Molecular Phylogeny of the Cicadas (Hemiptera: Cicadidae) with a Review of Tribe and Subfamily Classification
Zootaxa 4424 (1): 001–064 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2018 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4424.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:9339A2CB-C106-4C0E-9A94-1E5BB220335A ZOOTAXA 4424 A molecular phylogeny of the cicadas (Hemiptera: Cicadidae) with a review of tribe and subfamily classification DAVID C. MARSHALL1,15, MAX MOULDS2, KATHY B. R. HILL1, BENJAMIN W. PRICE3, ELIZABETH J. WADE4, CHRISTOPHER L. OWEN5, GEERT GOEMANS1,10, KIRAN MARATHE6,11, VIVEK SARKAR6,12, JOHN R. COOLEY1,7, ALLEN F. SANBORN8, KRUSHNAMEGH KUNTE6,13, MARTIN H. VILLET9 & CHRIS SIMON1,14 1Dept. of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269, USA 2Australian Museum Research Institute, 1 William Street, Sydney NSW 2010, Australia. E-mail: [email protected] 3Natural History Museum, London, United Kingdom. E-mail: [email protected] 4Dept. of Natural Science and Mathematics, Curry College, Milton, MA 02186, USA. E-mail: [email protected] 5Systematic Entomology Laboratory, Agricultural Research Service, U.S. Dept. of Agriculture, Beltsville, MD 20705, USA. E-mail: [email protected] 6National Centre for Biological Sciences, Tata Institute of Fundamental Research, GKVK Campus, Bellary Road, Bangalore 560 065, India 7College of Integrative Sciences, Wesleyan University, Middletown, CT 06459, USA. E-mail: [email protected] 8Dept. of Biology, Barry University, 11300 NE Second Avenue, Miami Shores, FL 33161, USA. E-mail: [email protected] 9Dept. of Biology, Rhodes University, Grahamstown 6140, South Africa. E-mail: [email protected] 10E-mail: [email protected] 11E-mail: [email protected] 12E-mail: [email protected] 13E-mail: [email protected] 14E-mail: [email protected] 15Corresponding author. -
Appendix 3A, Life Histories of Biota of Concern 1 Appendix 3A
Appendix 3A, Life Histories of Biota of Concern 1 Appendix 3A. Brief life histories for biota of concern: Aquatic invertebrates, fishes, and plants Life history attributes are critical to the analysis and characterization of risk associated with biota transfers, be those biological invasions or shifts in metapopulations that are potentially influenced by interbasin water diversions. While a comprehensive characterization of life history for each biota of concern is precluded by the scope of this investigation and number of biota of concern identified during problem formulation, the life histories that follow are focused on invasive attributes, historical accounts of past invasions, and the current distribution of the species. Existing literature sources in the scientific literature and peer-reviewed public domain provide ample background on each species of interest to the current investigation, with natural resource agencies and the applied research community having disseminated a wealth of data and information for use in these initial investigations of risks associated with biota transfers potentially resulting from interbasin water diversions. An ability to successfully translocate and accommodate to “new territory” is highly variable across species. Invasiveness depends on attributes related to physiological tolerance, and morphological and behavioral traits that directly or indirectly influence reproductive fitness of the species, thus enabling a species to establish and maintain sustainable populations in a region outside its current