Ripiphoridae (Coleoptera) of Greece and Turkey, with Notes on Their Distribution in the Eastern Mediterranean and Some Neighbouring Countries
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Elytra Reduction May Affect the Evolution of Beetle Hind Wings
Zoomorphology https://doi.org/10.1007/s00435-017-0388-1 ORIGINAL PAPER Elytra reduction may affect the evolution of beetle hind wings Jakub Goczał1 · Robert Rossa1 · Adam Tofilski2 Received: 21 July 2017 / Revised: 31 October 2017 / Accepted: 14 November 2017 © The Author(s) 2017. This article is an open access publication Abstract Beetles are one of the largest and most diverse groups of animals in the world. Conversion of forewings into hardened shields is perceived as a key adaptation that has greatly supported the evolutionary success of this taxa. Beetle elytra play an essential role: they minimize the influence of unfavorable external factors and protect insects against predators. Therefore, it is particularly interesting why some beetles have reduced their shields. This rare phenomenon is called brachelytry and its evolution and implications remain largely unexplored. In this paper, we focused on rare group of brachelytrous beetles with exposed hind wings. We have investigated whether the elytra loss in different beetle taxa is accompanied with the hind wing shape modification, and whether these changes are similar among unrelated beetle taxa. We found that hind wings shape differ markedly between related brachelytrous and macroelytrous beetles. Moreover, we revealed that modifications of hind wings have followed similar patterns and resulted in homoplasy in this trait among some unrelated groups of wing-exposed brachelytrous beetles. Our results suggest that elytra reduction may affect the evolution of beetle hind wings. Keywords Beetle · Elytra · Evolution · Wings · Homoplasy · Brachelytry Introduction same mechanism determines wing modification in all other insects, including beetles. However, recent studies have The Coleoptera order encompasses almost the quarter of all provided evidence that formation of elytra in beetles is less currently known animal species (Grimaldi and Engel 2005; affected by Hox gene than previously expected (Tomoyasu Hunt et al. -
Coleoptera: Tenebrionoidea)
ACTA ENTOMOLOGICA MUSEI NATIONALIS PRAGAE Published 30.vi.2010 Volume 50(1), pp. 157–166 ISSN 0374-1036 A review of Ripiphoridae in the Arabian Peninsula (Coleoptera: Tenebrionoidea) Jan BATELKA Nad Vodovodem 16, CZ-100 00 Praha 10, Czech Republic; e-mail: [email protected] Abstract. Distribution of the Ripiphoridae (Coleoptera: Tenebrionoidea) in the Arabian Peninsula is evaluated. Six species belonging to the genera Macrosiagon Hentz, 1830 and Ripiphorus Bosc, 1791 are fi gured and keyed, and the distribution of each species is mapped. Including new and previously published records, the Ripiphoridae are now reported from 19 localities of the Arabian Peninsula and offshore islands. Coordinates for each exact locality are given. Key words. Coleoptera, Tenebrionoidea, Ripiphoridae, Ripiphorinae, Macrosia- gon, Ripiphorus, faunistics, Arabian Peninsula, Palaearctic Region Introduction The Ripiphoridae (Coleoptera: Tenebrionoidea) are a cosmopolitan group of parasitoids, whose biogeography is only poorly understood. Only scarce distributional data are usually available because of their cryptic way of life in larval stages and short-lived adults. The Arabian Peninsula plays an important role in the understanding of their distribution in the Old World, as it is a transitional zone among three main zoogeographical realms: Afrotropical, Oriental and Palaearctic. The aim of this paper is to provide basis for further studies of the Ripiphoridae in this part of Asia and to make further research easier for those students who are not familiar with these rarely collected beetles. Each species is keyed and fi gured based on specimens collected in the Arabian Peninsula, with emphasis on colour variability and also on sexual dimorphism where appropriate. -
The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al. -
Wedge-Shaped Beetles (Suggested Common Name) Ripiphorus Spp. (Insecta: Coleoptera: Ripiphoridae)1 David Owens, Ashley N
EENY613 Wedge-Shaped Beetles (suggested common name) Ripiphorus spp. (Insecta: Coleoptera: Ripiphoridae)1 David Owens, Ashley N. Mortensen, Jeanette Klopchin, William Kern, and Jamie D. Ellis2 Introduction Ripiphoridae are a family of unusual parasitic beetles that are thought to be related to tumbling flower beetles (Coleoptera: Mordellidae) and blister beetles (Coleoptera: Meloidae). There is disagreement over the spelling of the family (Ripiphoridae) and genus (Ripiphorus) names. Here we use the original spelling that starts with only the letter Figure 1. Adult specimens of the two genera of Ripiphoridae. A) “R”; however, an initial “Rh” has also been used in the Macrosiagon Hentz, and B) Ripiphorus Bosc. scientific community (Rhipiphoridae and Rhipiphorus). Credits: Allen M. Boatman There are an estimated 35 nearctic species of Ripiphorus, Generally, the biology of the family Ripiphoridae is poorly two of which have been collected in Florida: Ripiphorus known. Ripiphorids parasitize bees and wasps (Hymenop- schwarzi LeConte (Figure 2A) and Ripiphorus fasciatus Say tera), roaches (Blattodea), and wood-boring beetles (Co- (Figure 2B). Due to limited information for both of these leoptera). However, the specific hosts for many ripiphorid species, the information presented below is characteristic species are unknown. Furthermore, only one sex (either of the genus Ripiphorus. Information specific to Ripiphorus male or female) has been described for several species, and fasciatus and Ripiphorus schwarzi is presented where the males and females of some species look different. detailed information is available. Two genera of Ripiphoridae infest hymenopteran (bee and wasp) nests: Macrosiagon Hentz (Figure 1A) and Ripiphorus Bosc (formerly Myodites Latreille) (Figure 1B). Species of Macrosiagon are parasites of a variety of hymenopteran families including: Halictidae, Vespidae, Tiphiidae, Apidae, Pompilidae, Crabronidae, and Sphecidae. -
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 -
André Nel Sixtieth Anniversary Festschrift
Palaeoentomology 002 (6): 534–555 ISSN 2624-2826 (print edition) https://www.mapress.com/j/pe/ PALAEOENTOMOLOGY PE Copyright © 2019 Magnolia Press Editorial ISSN 2624-2834 (online edition) https://doi.org/10.11646/palaeoentomology.2.6.1 http://zoobank.org/urn:lsid:zoobank.org:pub:25D35BD3-0C86-4BD6-B350-C98CA499A9B4 André Nel sixtieth anniversary Festschrift DANY AZAR1, 2, ROMAIN GARROUSTE3 & ANTONIO ARILLO4 1Lebanese University, Faculty of Sciences II, Department of Natural Sciences, P.O. Box: 26110217, Fanar, Matn, Lebanon. Email: [email protected] 2State Key Laboratory of Palaeobiology and Stratigraphy, Center for Excellence in Life and Paleoenvironment, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, China. 3Institut de Systématique, Évolution, Biodiversité, ISYEB-UMR 7205-CNRS, MNHN, UPMC, EPHE, Muséum national d’Histoire naturelle, Sorbonne Universités, 57 rue Cuvier, CP 50, Entomologie, F-75005, Paris, France. 4Departamento de Biodiversidad, Ecología y Evolución, Facultad de Biología, Universidad Complutense, Madrid, Spain. FIGURE 1. Portrait of André Nel. During the last “International Congress on Fossil Insects, mainly by our esteemed Russian colleagues, and where Arthropods and Amber” held this year in the Dominican several of our members in the IPS contributed in edited volumes honoring some of our great scientists. Republic, we unanimously agreed—in the International This issue is a Festschrift to celebrate the 60th Palaeoentomological Society (IPS)—to honor our great birthday of Professor André Nel (from the ‘Muséum colleagues who have given us and the science (and still) national d’Histoire naturelle’, Paris) and constitutes significant knowledge on the evolution of fossil insects a tribute to him for his great ongoing, prolific and his and terrestrial arthropods over the years. -
Read the Decision
Decision Date 5 February 2021 Application number APP203875 Application type To import for release and/or release from containment any new organism under section 34 of the Hazardous Substances and New Organisms Act 1996 Applicant Tasman District Council Date of hearing/consideration 17 December 2020 Date Application received 14 September 2020 Considered by A decision-making committee of the Environmental Protection Authority (the Committee)1 Dr Nick Roskruge (Chair) Dr John Taylor Mr Peter Cressey Purpose of the application To import and release two parasitoids, Metoecus paradoxus and Volucella inanis as biological control agents for the invasive German and common wasps (Vespula germanica and V. vulgaris). New organism approved Metoecus paradoxus Linnaeus 1761 Volucella inanis Linnaeus 1758 1 The Committee referred to in this decision is the subcommittee that has made the decision on this application under delegated authority in accordance with section 18A of the Act. Decision APP203875 Summary of decision 1. Application APP203875 to import and release two parasitoids, Metoecus paradoxus and Volucella inanis, as biological control agents (BCAs) for the invasive German and common wasps (Vespula germanica and V. vulgaris), in New Zealand, was lodged under section 34 of the Hazardous Substances and New Organisms Act 1996 (the Act). 2. The application was considered in accordance with the relevant provisions of the Act and of the HSNO (Methodology) Order 1998 (the Methodology). 3. The Committee has approved the application in accordance with section 38(1)(a) of the Act. Application and consideration process 4. The application was formally received on 14 September 2020. 5. The applicant, Tasman District Council, applied to the Environmental Protection Authority (EPA) to import and release two parasitoids, Metoecus paradoxus and Volucella inanis, as BCAs for the invasive German and common wasps (Vespula germanica and V. -
Insect Classification Standards 2020
RECOMMENDED INSECT CLASSIFICATION FOR UGA ENTOMOLOGY CLASSES (2020) In an effort to standardize the hexapod classification systems being taught to our students by our faculty in multiple courses across three UGA campuses, I recommend that the Entomology Department adopts the basic system presented in the following textbook: Triplehorn, C.A. and N.F. Johnson. 2005. Borror and DeLong’s Introduction to the Study of Insects. 7th ed. Thomson Brooks/Cole, Belmont CA, 864 pp. This book was chosen for a variety of reasons. It is widely used in the U.S. as the textbook for Insect Taxonomy classes, including our class at UGA. It focuses on North American taxa. The authors were cautious, presenting changes only after they have been widely accepted by the taxonomic community. Below is an annotated summary of the T&J (2005) classification. Some of the more familiar taxa above the ordinal level are given in caps. Some of the more important and familiar suborders and families are indented and listed beneath each order. Note that this is neither an exhaustive nor representative list of suborders and families. It was provided simply to clarify which taxa are impacted by some of more important classification changes. Please consult T&J (2005) for information about taxa that are not listed below. Unfortunately, T&J (2005) is now badly outdated with respect to some significant classification changes. Therefore, in the classification standard provided below, some well corroborated and broadly accepted updates have been made to their classification scheme. Feel free to contact me if you have any questions about this classification. -
ACTA ENTOMOLOGICA 59(2): 569–582 MUSEI NATIONALIS PRAGAE Doi: 10.2478/Aemnp-2019-0050
2019 ACTA ENTOMOLOGICA 59(2): 569–582 MUSEI NATIONALIS PRAGAE doi: 10.2478/aemnp-2019-0050 ISSN 1804-6487 (online) – 0374-1036 (print) www.aemnp.eu CONFERENCE ABSTRACTS Abstracts of the Immature Beetles Meeting 2019 October 3–4, Prague, Czech Republic Matthias SEIDEL1,2), Emmanuel ARRIAGA-VARELA1) & Dominik VONDRÁČEK1,2) (editors) 1) Department of Zoology, Faculty of Science, Charles University in Prague, Viničná 7, CZ-128 43, Prague 2, Czech Republic 2) Department of Entomology, National Museum, Cirkusová 1740, CZ-191 00 Praha 9, Czech Republic e-mail: [email protected] Accepted: 10th November 2019; Published online: 27th December 2019. Zoobank: http://zoobank.org/urn:lsid:zoobank.org:pub:082BDE6B-0493-4B64-9689-0A91A2DB5424 © 2019 The Authors. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Licence. The seventh Immature Beetles Meeting was held in Beetles Meeting, the discussion about beetle topics conti- Prague on October 3–4, 2019 at the Faculty of Science nued in traditional Prague pubs on both evenings. of the Charles University in Prague. It was organized We proudly report that the meeting fulfi lled again its pri- in cooperation with the Department of Entomology of mary aim – to bringing both established and newly starting the National Museum and the Crop Research Institute scientists and students who share an interest in immature in Prague. In total, 58 participants from Asia, Europe stages of beetles and associated topics. We hope that the and North and South America attended the meeting (see participants were able to gain new insights into the fi eld the list of participants and group photo in Fig. -
Helminth Parasites of the Common Grackle Quiscalus Quiscula Versicolor Vieillot in Indiana
This dissertation has been 62—3609 microfilmed exactly as received WELKER, George William, 1923- HELMINTH PARASITES OF THE COMMON GRACKLE QUISCALUS QUISCULA VERSICOLOR VIEILLOT IN INDIANA. The Ohio State University, Ph.D., 1962 Zoology University Microfilms, Inc., Ann Arbor, Michigan HELMINTH PARASITES OP THE COMMON GRACKLE QUISCALU5 QUISCULA VERSICOLOR VIEILLOT IN INDIANA DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By George William Welker, B. S., M. A. u _ u u u The Ohio State University 1962 Approved by: 1'XJijdJi ~7 Adviser urtameenhtt of Zoology and Entomology Dedicated as a tribute of appreciation and admiration to ELLEN ANN, my wife, for her help and for the sacrifices which she made during the four years covered by this study. ii ACKNOWLEDGMENTS The author wishes to express his sincere appreciation for all the help and cooperation which he has received from many people during the course of this study: Dr. Joseph Jones, Jr. of St. Augustine's College, Raleigh, North Carolina; Dr. Donal Myer, Southern Illinois university; Dr. E. J. Robinson, Jr., Kenyon College, Gambier, Ohio; Dr. Martin J. Ulmer, Iowa State University, Ames, Iowa; and Dr. A. Carter Broad and Dr. Carl Reese of the reading committee who helped in checking the paper for errors. Special acknowledgment goes to two persons whose help and influence are most deeply appreciated. To Professor Robert H. Cooper, Head of the Department of Science at Ball State Teachers College, whose sincere and continuous interest, encouragement and help made possible the completion of the work; and to Professor Joseph N. -
Encyclopedia of Social Insects
G Guests of Social Insects resources and homeostatic conditions. At the same time, successful adaptation to the inner envi- Thomas Parmentier ronment shields them from many predators that Terrestrial Ecology Unit (TEREC), Department of cannot penetrate this hostile space. Social insect Biology, Ghent University, Ghent, Belgium associates are generally known as their guests Laboratory of Socioecology and Socioevolution, or inquilines (Lat. inquilinus: tenant, lodger). KU Leuven, Leuven, Belgium Most such guests live permanently in the host’s Research Unit of Environmental and nest, while some also spend a part of their life Evolutionary Biology, Namur Institute of cycle outside of it. Guests are typically arthropods Complex Systems, and Institute of Life, Earth, associated with one of the four groups of eusocial and the Environment, University of Namur, insects. They are referred to as myrmecophiles Namur, Belgium or ant guests, termitophiles, melittophiles or bee guests, and sphecophiles or wasp guests. The term “myrmecophile” can also be used in a broad sense Synonyms to characterize any organism that depends on ants, including some bacteria, fungi, plants, aphids, Inquilines; Myrmecophiles; Nest parasites; and even birds. It is used here in the narrow Symbionts; Termitophiles sense of arthropods that associated closely with ant nests. Social insect nests may also be parasit- Social insect nests provide a rich microhabitat, ized by other social insects, commonly known as often lavishly endowed with long-lasting social parasites. Although some strategies (mainly resources, such as brood, retrieved or cultivated chemical deception) are similar, the guests of food, and nutrient-rich refuse. Moreover, nest social insects and social parasites greatly differ temperature and humidity are often strictly regu- in terms of their biology, host interaction, host lated. -
Coleoptera: Ripiphoridae: Ripiphorinae)
Eur. J. Entomol. 101: 577–581, 2004 ISSN 1210-5759 Two new wedge-shaped beetles in Albo-Cenomanian ambers of France (Coleoptera: Ripiphoridae: Ripiphorinae) VINCENT PERRICHOT1, ANDRÉ NEL2* and DIDIER NÉRAUDEAU1 1 Géosciences Rennes and CNRS UMR 6118, Université Rennes 1, bât. 15, 263, avenue du Général Leclerc, 35042 Rennes Cedex, France; e-mails: [email protected], [email protected] 2 Entomologie and CNRS UMR 5143, Muséum National d’Histoire Naturelle, 45, rue Buffon, F-75005, Paris, France; e-mail: [email protected] Key words. Coleoptera, Ripiphoridae, Ripiphorinae, new genus, new species, amber fossil, Albian, Cenomanian, Archingeay, Salignac, France Abstract. Paleoripiphorus deploegi gen. n., sp. n. and Macrosiagon ebboi sp. n., described from two French Albo-Cenomanian ambers (mid Cretaceous), are the oldest definitely identified representatives of the Ripiphoridae: Ripiphorinae. They belong to or are closely related to extant genera of this coleopteran subfamily. Together with Myodites burmiticus Cockerell, 1917 from the Albian Burmese amber, they demonstrate that the group is distinctly older than suggested by the hitherto available fossil record. By infer- ence after the biology of the extant Ripiphorinae, Macrosiagon ebboi may have been parasitic on wasps and Paleoripiphorus deploegi on bees, suggesting that Apoidea may have been present in the Lower Cretaceous. INTRODUCTION FAMILY RIPIPHORIDAE The Ripiphoridae is a small family of parasitic beetles Subfamily Ripiphorinae rather poorly represented in the fossil record, mainly by Genus Paleoripiphorus gen. n. species from the Eocene Baltic amber (Spahr, 1981) and the Paleogene of Florissant (Colorado, USA) (Scudder, Type species. Paleoripiphorus deploegi sp. n. 1890; Meyer, 2003).