Prostomis Mandibularis F. (Coleoptera: Prostomidae
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Keys to Families of Beetles in America North of Mexico
816 · Key to Families Keys to Families of Beetles in America North of Mexico by Michael A. Ivie hese keys are specifically designed for North American and, where possible, overly long lists of options, but when nec- taxa and may lead to incorrect identifications of many essary, I have erred on the side of directing the user to a correct Ttaxa from outside this region. They are aimed at the suc- identification. cessful family placement of all beetles in North America north of No key will work on all specimens because of abnormalities Mexico, and as such will not always be simple to use. A key to the of development, poor preservation, previously unknown spe- most common 50% of species in North America would be short cies, sexes or variation, or simple errors in characterization. Fur- and simple to use. However, after an initial learning period, most thermore, with more than 30,000 species to be considered, there coleopterists recognize those groups on sight, and never again are undoubtedly rare forms that escaped my notice and even key them out. It is the odd, the rare and the exceptional that make possibly some common and easily collected species with excep- a complex key necessary, and it is in its ability to correctly place tional characters that I overlooked. While this key should work those taxa that a key is eventually judged. Although these keys for at least 95% of specimens collected and 90% of North Ameri- build on many previous successful efforts, especially those of can species, the specialized collector who delves into unique habi- Crowson (1955), Arnett (1973) and Borror et al. -
The Evolution and Genomic Basis of Beetle Diversity
The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State -
Current Classification of the Families of Coleoptera
The Great Lakes Entomologist Volume 8 Number 3 - Fall 1975 Number 3 - Fall 1975 Article 4 October 1975 Current Classification of the amiliesF of Coleoptera M G. de Viedma University of Madrid M L. Nelson Wayne State University Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation de Viedma, M G. and Nelson, M L. 1975. "Current Classification of the amiliesF of Coleoptera," The Great Lakes Entomologist, vol 8 (3) Available at: https://scholar.valpo.edu/tgle/vol8/iss3/4 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. de Viedma and Nelson: Current Classification of the Families of Coleoptera THE GREAT LAKES ENTOMOLOGIST CURRENT CLASSIFICATION OF THE FAMILIES OF COLEOPTERA M. G. de viedmal and M. L. els son' Several works on the order Coleoptera have appeared in recent years, some of them creating new superfamilies, others modifying the constitution of these or creating new families, finally others are genera1 revisions of the order. The authors believe that the current classification of this order, incorporating these changes would prove useful. The following outline is based mainly on Crowson (1960, 1964, 1966, 1967, 1971, 1972, 1973) and Crowson and Viedma (1964). For characters used on classification see Viedma (1972) and for family synonyms Abdullah (1969). Major features of this conspectus are the rejection of the two sections of Adephaga (Geadephaga and Hydradephaga), based on Bell (1966) and the new sequence of Heteromera, based mainly on Crowson (1966), with adaptations. -
From Tethyan-Influenced Cretaceous Ambers
Geoscience Frontiers 7 (2016) 695e706 HOSTED BY Contents lists available at ScienceDirect China University of Geosciences (Beijing) Geoscience Frontiers journal homepage: www.elsevier.com/locate/gsf Research paper Evolutionary and paleobiological implications of Coleoptera (Insecta) from Tethyan-influenced Cretaceous ambers David Peris a,*, Enrico Ruzzier b, Vincent Perrichot c, Xavier Delclòs a a Departament de Dinàmica de la Terra i de l’Oceà and Institut de Recerca de la Biodiversitat (IRBio), Facultat de Geologia, Universitat de Barcelona, Martí i Franques s/n, 08071 Barcelona, Spain b Department of Life Science, Natural History Museum, Cromwell Rd, SW7 5BD London, UK c UMR CNRS 6118 Géosciences & OSUR, Université de Rennes 1, 35042 Rennes cedex, France article info abstract Article history: The intense study of coleopteran inclusions from Spanish (Albian in age) and French (AlbianeSantonian Received 23 September 2015 in age) Cretaceous ambers, both of Laurasian origin, has revealed that the majority of samples belong to Received in revised form the Polyphaga suborder and, in contrast to the case of the compression fossils, only one family of 25 December 2015 Archostemata, one of Adephaga, and no Myxophaga suborders are represented. A total of 30 families Accepted 30 December 2015 from Spain and 16 families from France have been identified (with almost twice bioinclusions identified Available online 16 January 2016 in Spain than in France); 13 of these families have their most ancient representatives within these ambers. A similar study had previously only been performed on Lebanese ambers (Barremian in age and Keywords: Beetle Gondwanan in origin), recording 36 coleopteran families. Few lists of taxa were available for Myanmar Fossil (Burmese) amber (early Cenomanian in age and Laurasian in origin). -
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Memoirs of the Museum of Victoria 56(2):659-666 (1997) 28 February 1997 https://doi.org/10.24199/j.mmv.1997.56.67 BIODIVERSITY OF NEW ZEALAND BEETLES (INSECTA, COLEOPTERA) J. KLIMASZEWSK.I Manaaki Whenua — Landcare Research, Private Bag 92170, Auckland, New Zealand Present address: BC Research. 3650 Weshrook Mall, Vancouver V6S SLS, Canada Abstract Klimaszewski, J., 1 997. Biodiversity of New Zealand beetles (Insecta: Coleoptera). Memoirs of the Museum of Victoria 56(2): 659-666. Approximately 5235 species are described for New Zealand, including 354 introduced. They belong to 82 families in two suborders, Adephaga and Polyphaga. The New Zealand beetle fauna is distinguished by the absence of many major lineages, a high level of endem- ism. which in many groups is over 90% at the specific level and over 43% at the generic level (e.g.. Staphylinidae), and the radiation of many groups of genera and species. The origins of New Zealand's beetle fauna are still poorly understood. They are likely to be varied, includ- ing Gondwanan elements and elements which arrived here by short and long-distance dispersal recently and in the remote past. The size of the New Zealand beetle fauna is con- sistent with species number/land area relationships in other areas around the world. Introduction Zealand beetles is that of Kuschel (1990), in the suburb of Lynfield, Auckland, in which 982 The beetles are the largest order of organisms, beetle species were recorded in a diverse veg- with over 350 000 described species world- etation including remnant forest, pastureland, wide. and suburban garden. -
Utilization of Non-Native Wood by Saproxylic Insects
Chapter 23 Utilization of Non-native Wood by Saproxylic Insects Michael D. Ulyshen, Stephen M. Pawson, Manuela Branco, Scott Horn, E. Richard Hoebeke, and Martin M. Gossner Abstract Whether intentionally or accidentally introduced, non-native woody plants now feature prominently in many ecosystems throughout the world. The dying and deadwood produced by these plants represent novel resources for saproxylic insects, but their suitability to these organisms remains poorly under- stood. We herein review existing knowledge about the utilization of non-native wood species by saproxylic insect communities and also provide several previously unpublished case studies from the USA, Germany, Portugal/Spain, and New Zealand. The first case study suggests that the relative number of beetle species utilizing non-native vs. native wood varies greatly among wood species, with some non-native species (e.g., Albizia julibrissin) supporting a high beetle diversity. A decomposition experiment found that termites did not readily attack three non-native wood species and did not contribute significantly to their decomposition in contrast to what has been shown for a native pine species. The second case study found two species of non-native wood to support a lower richness of beetles compared to two native wood species in Germany, with Pseudotsuga menziesii supporting particu- larly few species which formed just a small subset of the community collected from native Picea abies. The third case study, from Iberia, found Eucalyptus to support a relatively small number of insect species with generalist host preferences. The fourth M. D. Ulyshen (*) · S. Horn USDA Forest Service, Southern Research Station, Athens, GA, USA e-mail: [email protected] S. -
Burmese Amber Taxa
Burmese (Myanmar) amber taxa, on-line checklist v.2018.1 Andrew J. Ross 15/05/2018 Principal Curator of Palaeobiology Department of Natural Sciences National Museums Scotland Chambers St. Edinburgh EH1 1JF E-mail: [email protected] http://www.nms.ac.uk/collections-research/collections-departments/natural-sciences/palaeobiology/dr- andrew-ross/ This taxonomic list is based on Ross et al (2010) plus non-arthropod taxa and published papers up to the end of April 2018. It does not contain unpublished records or records from papers in press (including on- line proofs) or unsubstantiated on-line records. Often the final versions of papers were published on-line the year before they appeared in print, so the on-line published year is accepted and referred to accordingly. Note, the authorship of species does not necessarily correspond to the full authorship of papers where they were described. The latest high level classification is used where possible though in some cases conflicts were encountered, usually due to cladistic studies, so in these cases an older classification was adopted for convenience. The classification for Hexapoda follows Nicholson et al. (2015), plus subsequent papers. † denotes extinct orders and families. New additions or taxonomic changes to the previous list (v.2017.4) are marked in blue, corrections are marked in red. The list comprises 37 classes (or similar rank), 99 orders (or similar rank), 510 families, 713 genera and 916 species. This includes 8 classes, 64 orders, 467 families, 656 genera and 849 species of arthropods. 1 Some previously recorded families have since been synonymised or relegated to subfamily level- these are included in parentheses in the main list below. -
Cucujidae (Coleoptera: Cucujoidea) — a New Family to the Fauna Of
Cucujidae (Coleoptera: Cucujoidea) – a new family... 93 Historia naturalis bulgarica, 19: 93-97, 2008 Cucujidae (Coleoptera: Cucujoidea) – a new family to the fauna of Bulgaria Borislav GUÉORGUIEV, Danail DOYCHEV, Dinko OVCHAROV GUÉORGUIEV B., Doychev D., Ovcharov D. 2008. Cucujidae (Coleoptera: Cucujoidea – a new family to the fauna of Bulgaria. – Historia naturalis bulgarica, 19: 93-97. Abstract. The family Cucujidae Latreille, the genus Cucujus Fabricius, and the species C. cinnaberinus (Scopoli) are recorded for the first time in the fauna of Bulgaria. Key words: Coleoptera, Cucujidae, Cucujus, first records, Bulgaria. At least 119 families of Coleoptera, in the sense of the classifications of HANSEN (1991), BROWNE & SCHOLTZ (1995) and LAWRENCE & NEWTON (1995) inhabit Bulgaria. Until this communication we had no records for the country only for Cerophytidae, Phloiophilidae, Phloeostichidae, Cucujidae, Prostomidae, and Boridae. The Cucujidae Latreille, 1802, sometimes called “flat bark beetles” are a family of distinctively flat beetles found worldwide under the bark of dead and living trees. The family is one of the smallest ones and consists of 47 species distributed in four genera (THOMAS, 1999; LEE & SATÔ, 2007). Cucujidae have elongate parallel-side bodies ranging from 6 to 25 mm in length. Most are brown colored, while others are black, reddish or yellow. Head is triangular in shape, with filiform antennae of 11 antennomeres, and large mandibles. The pronotum is narrower than the head. Both larvae and adults live under the bark, otherwise little is known of their habits. The family was formerly larger, with subfamilies Laemophloeinae, Silvanainae, and Passandrinae (and some tenebrionid genera to boot), but recent revision has raised the subfamilies to family status (PAKALUK et al., 1994; LAWRENCE & NEWTON, 1995). -
Fossil Perspectives on the Evolution of Insect Diversity
FOSSIL PERSPECTIVES ON THE EVOLUTION OF INSECT DIVERSITY Thesis submitted by David B Nicholson For examination for the degree of PhD University of York Department of Biology November 2012 1 Abstract A key contribution of palaeontology has been the elucidation of macroevolutionary patterns and processes through deep time, with fossils providing the only direct temporal evidence of how life has responded to a variety of forces. Thus, palaeontology may provide important information on the extinction crisis facing the biosphere today, and its likely consequences. Hexapods (insects and close relatives) comprise over 50% of described species. Explaining why this group dominates terrestrial biodiversity is a major challenge. In this thesis, I present a new dataset of hexapod fossil family ranges compiled from published literature up to the end of 2009. Between four and five hundred families have been added to the hexapod fossil record since previous compilations were published in the early 1990s. Despite this, the broad pattern of described richness through time depicted remains similar, with described richness increasing steadily through geological history and a shift in dominant taxa after the Palaeozoic. However, after detrending, described richness is not well correlated with the earlier datasets, indicating significant changes in shorter term patterns. Corrections for rock record and sampling effort change some of the patterns seen. The time series produced identify several features of the fossil record of insects as likely artefacts, such as high Carboniferous richness, a Cretaceous plateau, and a late Eocene jump in richness. Other features seem more robust, such as a Permian rise and peak, high turnover at the end of the Permian, and a late-Jurassic rise. -
An Annotated List of Insects and Other Arthropods
This file was created by scanning the printed publication. Text errors identified by the software have been corrected; however, some errors may remain. Invertebrates of the H.J. Andrews Experimental Forest, Western Cascade Range, Oregon. V: An Annotated List of Insects and Other Arthropods Gary L Parsons Gerasimos Cassis Andrew R. Moldenke John D. Lattin Norman H. Anderson Jeffrey C. Miller Paul Hammond Timothy D. Schowalter U.S. Department of Agriculture Forest Service Pacific Northwest Research Station Portland, Oregon November 1991 Parson, Gary L.; Cassis, Gerasimos; Moldenke, Andrew R.; Lattin, John D.; Anderson, Norman H.; Miller, Jeffrey C; Hammond, Paul; Schowalter, Timothy D. 1991. Invertebrates of the H.J. Andrews Experimental Forest, western Cascade Range, Oregon. V: An annotated list of insects and other arthropods. Gen. Tech. Rep. PNW-GTR-290. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station. 168 p. An annotated list of species of insects and other arthropods that have been col- lected and studies on the H.J. Andrews Experimental forest, western Cascade Range, Oregon. The list includes 459 families, 2,096 genera, and 3,402 species. All species have been authoritatively identified by more than 100 specialists. In- formation is included on habitat type, functional group, plant or animal host, relative abundances, collection information, and literature references where available. There is a brief discussion of the Andrews Forest as habitat for arthropods with photo- graphs of representative habitats within the Forest. Illustrations of selected ar- thropods are included as is a bibliography. Keywords: Invertebrates, insects, H.J. Andrews Experimental forest, arthropods, annotated list, forest ecosystem, old-growth forests. -
Comparative Study of Larvae of Tenebrionoidea (Coleoptera: Cucujiformia)
Eur. J. Entomol. 102: 241–264, 2005 ISSN 1210-5759 Comparative study of larvae of Tenebrionoidea (Coleoptera: Cucujiformia) ROLF GEORG BEUTEL and FRANK FRIEDRICH Institut für Spezielle Zoologie und Evolutionsbiologie, FSU Jena, 07743 Jena, Germany; e-mails: [email protected], [email protected] Key words. Tenebrionoidea, larvae, morphology, character evolution, phylogeny Abstract. External and internal head structures and external structures of the thorax and abdomen of larval representatives of Melan- dryidae (Orchesia), Ulodidae (Meryx), Oedemeridae (Pseudolycus) and Pythidae (Pytho) are described. The obtained data were compared to characters of other tenebrionoid larvae and to larval characters of other representatives of Cucujiformia. Characters potentially relevant for phylogenetic reconstruction are listed and were analysed cladistically. The data set is characterised by a high degree of homoplasy and the resolution of the strict consensus trees of 2650 or 815 (second analysis) minimal length trees is low. The monophyly of Tenebrionoidea is supported by several larval autapomorphies, e.g. posteriorly diverging gula, anteriorly shifted posterior tentorial arms, asymmetric mandibles and the origin of several bundles of M. tentoriopharyngalis from the well-developed gular ridges. Several features of the larval head are plesiomorphic compared to the cleroid-cucujoid lineage. The interrelationships of most tenebrionoid families not belonging to the pythid-salpingid and anthicid-scraptiid groups were not resolved. Synchroidae were placed as sister group of a clade comprising these two lineages and Prostomidae. A sistergroup relationship between Trictenotomidae and Pythidae seems to be well supported and the monophyly of the anthicid-scraptiid lineage was also confirmed. Another potential clade comprises Prostomidae, Mycteridae and Boridae, and possibly Pyrochroidae (s.str.) and Inopeplinae. -
A Catalog of the Coleóptera of America North of Mexico Family: Micromalthidae
//w^ m^k. ^ 3 A CATALOG OF THE COLEÓPTERA OF AMERICA NORTH OF MEXICO FAMILY: MICROMALTHIDAE 0 J c > Co NAL Digitizing Project Ï ah5292 ,.^5^, UNITED STATES AGRICULTURE PREPARED BY (fk A AN DEPARTMENT OF HANDBOOK AGRICULTURAL AGRICULTURE NUMBER 529-2 RESEARCH SERVICE FAMILIES OF COLEóPTERA IN AMERICA NORTH OF MEXICO Fascicle ' Family Year issued Fascicle ' Family Year issued Fascicle ' Fumily Year issued 1 Cupedidac 1979 45 Chelonariidae 98 Endomychidae __ 2 Micromalthidae _ 1982 46 Callirhipidae 100 Lathridiidae 3 Carabidae 47 Heteroceridae ]1978 102 Biphyllidae 4 Rhysodidae 48 Limnichidae 103 Byturidae 5 Amphizoidae --- 49 Dryopidae 104 Mycetophagidae 6__ Haliplidae _ -_ 50 Elmidae 105 Ciidae 1982 8 Noteridae 51 Buprestidae 107 Prostomidae 9 Dytiscidae 52 Cebrionidae 10 Gyrinidae 53 Elateridae 109 Colydiidae 13 Sphaeriidae 54 Throscidae 110 Monommatidae 14 Hydroscaphidae 55 Cerophytidae 111 Cephaloidae 15 Hydraenidae 56 Perothopidae 112 Zopheridae 16 Hydrophilidae __ 57 Eucnemidae 115 Tenebrionidae ._ 17 Georyssidae 58 —Telegeusidae 116 Alleculidae 18_„.Sphaeritidae —- 61 Phengodidae 117 Lagriidae 20 Histeridae 62 Lampyridae 118 Salpingidae 21 Ptiliidae 63 Cantharidae 119 Mycteridae 22 Limulodidae 64 Lycidae 120 Pyrochroidae -__ 23 E>asyceridae —. 65 Derodontidae 121 Othniidae 24 Micropeplidae __ 66 Nosodendridae 122 Inopeplidae 25 .—Leptinidae 67 Dermestidae 123 Oedemeridae 26 Leiodidae 69 Ptinidae 124 Melandryidae __ 27 Scydmacnidae -- 70 Anobiidae 125 Mordellidae 28 Silphidae 71 Bostrichidae 126 Rhipiphoridae __ 29 Scaphidiidae 72