Coleoptera: Lymexylidae) from Honduras
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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. -
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. -
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 -
Coleoptera: Introduction and Key to Families
Royal Entomological Society HANDBOOKS FOR THE IDENTIFICATION OF BRITISH INSECTS To purchase current handbooks and to download out-of-print parts visit: http://www.royensoc.co.uk/publications/index.htm This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 2.0 UK: England & Wales License. Copyright © Royal Entomological Society 2012 ROYAL ENTOMOLOGICAL SOCIETY OF LONDON Vol. IV. Part 1. HANDBOOKS FOR THE IDENTIFICATION OF BRITISH INSECTS COLEOPTERA INTRODUCTION AND KEYS TO FAMILIES By R. A. CROWSON LONDON Published by the Society and Sold at its Rooms 41, Queen's Gate, S.W. 7 31st December, 1956 Price-res. c~ . HANDBOOKS FOR THE IDENTIFICATION OF BRITISH INSECTS The aim of this series of publications is to provide illustrated keys to the whole of the British Insects (in so far as this is possible), in ten volumes, as follows : I. Part 1. General Introduction. Part 9. Ephemeroptera. , 2. Thysanura. 10. Odonata. , 3. Protura. , 11. Thysanoptera. 4. Collembola. , 12. Neuroptera. , 5. Dermaptera and , 13. Mecoptera. Orthoptera. , 14. Trichoptera. , 6. Plecoptera. , 15. Strepsiptera. , 7. Psocoptera. , 16. Siphonaptera. , 8. Anoplura. 11. Hemiptera. Ill. Lepidoptera. IV. and V. Coleoptera. VI. Hymenoptera : Symphyta and Aculeata. VII. Hymenoptera: Ichneumonoidea. VIII. Hymenoptera : Cynipoidea, Chalcidoidea, and Serphoidea. IX. Diptera: Nematocera and Brachycera. X. Diptera: Cyclorrhapha. Volumes 11 to X will be divided into parts of convenient size, but it is not possible to specify in advance the taxonomic content of each part. Conciseness and cheapness are main objectives in this new series, and each part will be the work of a specialist, or of a group of specialists. -
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. -
Biodiversity of Coleopteran Insects (Insecta, Coleoptera) in the Tugai
International Journal of Academic and Applied Research (IJAAR) ISSN: 2643-9603 Vol. 4 Issue 11, November - 2020, Pages: 30-33 Biodiversity of Coleopteran Insects (Insecta, Coleoptera) in the Tugai Forests of the Lower Amudarya State Biosphere Reserve 1Bekchanov Xudaybergan Urinovich, 2Duschanov Umar Egamberdiyevich, 3Komiljonova Gulrux Kudrat qizi. ¹Сandidate of Zoological Sciences,Urgench State University of Uzbekistan. ²Senior Lecturer at the Faculty of Natural Sciences, Urgench State University of Uzbekistan. ³Student of the Faculty of natural Sciences, Urgench State University of Uzbekistan. [email protected] Abstract. The paper presents the results of studies on the biodiversity of coleopteran insects (Insecta, Coleoptera) in the tugai forests of the Nizhne-Amudarya State Biosphere Reserve, as well as a review of the literature on this topic. There are 13 species of 4 families: Scarabaeidae, Lymexylidae, Buprestidae, Cerambycidae, which also includes previously published information on finds about the region. Keywords: coleoptera, beetle. Insecta, Scarabaeidae, Lymexylidae, Buprestidae, Cerambycidae. 1. INTRODUCTION. Coleoptera (Insecta: Coleóptera) are one of the most numerous and ecologically diverse orders of insects. Beetles are common in almost all landscape-geographical zones and inhabit most terrestrial ecosystems. The high abundance and confinement to different biotopes, sensitivity to changes in the ecological situation makes it possible to use beetles as a model group for studying the structure of communities in disturbed and reference territories. PHYSICAL AND GEOGRAPHICAL CHARACTERISTICS OF THE DISTRICT RESEARCH. The Lower Amudarya State Biosphere Reserve (NABR) was established in 2011 with the support of a joint project of the United Nations Development Program, the Global Environment Facility and the Government of the Republic of Karakalpakstan "Conservation of the tugai forests of Karakalpakstan in the Amudarya river delta" based on the Badai-Tugai nature reserve. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Report on Beetles (Coleoptera) and a Woodwasp Recorded from the Dartington Hall Estate, 2018 by Dr Martin Luff
Report on beetles (Coleoptera) and a woodwasp recorded from the Dartington Hall Estate, 2018 by Dr Martin Luff 1. Introduction and Methods The majority of beetle recording in 2018 was again concentrated on Berryman’s Marsh. Three bottle traps were used throughout the season from April to October, suspended above several of the dead wood habitat piles in the marsh. Another trap was also hung over a large pile of logs and woody brash in Mary Bartlett’s garden at 1, Martins. In the autumn, a similar trap was put on one of the large heaps of mowings left at the margin of Berryman’s Marsh after it was cut. The dry summer exposed a large area of mud around the main pond on Queen’s Marsh; this was colonised by a range of specialist beetle species that were sampled by searching and sieving on June 28th. Water beetles were also trapped in the first pond on Berryman’s Marsh in October using baited bottle traps. On June 26th, I accompanied Mike Newby and Vicky Churchill to Redlake Meadow and Whitely Field, for a first look at sites outside the core estate. 2. Results It was another very satisfactory season. The 245 beetle species recorded (28 more than in 2017) was the highest annual total since I started recording here. Of these, 67 (27.3%) were additions to the Dartington list: one is Nationally Rare (NR), formerly classified as Red Data Book (RDB) and eleven are Nationally Scarce (NS), formerly called Nationally Notable. Some interesting results from each area are summarised below. -
Deretaphrus Interruptus Head, Ventral; Fig
1. 2. Figures 1-2. Examples of ESEM images of metal incorporated mandibles. Fig. 1: Deretaphrus interruptus head, ventral; Fig. 2: Deretaphrus piceus head, anterior. 465 3. 4. 5. 6. 7. 8. 9. 10. Figures 3-10. Mandibles with incorporated metals. Fig. 3: Ambrosiodmus leconti rt. dorsal; Fig. 4: Ips grandicollis rt. dorsal; Fig. 5: Scolytus muticus rt. dorsal; Fig. 6: Myoplatypus flavicornis rt. dorsal; Fig. 7: Thanasimus dubius rt. dorsal; Fig. 8: Thanasimus dubius left ventral; Fig. 9: Stegobium paniceum rt. dorsal; Fig. 10: Stegobium paniceum left ventral. 466 1 30 2 14 31 32 3 15 33 26 27 28 29 4 34 16 35 17 36 38 5 37 39 40 18 6 41 42 43 19 44 45 7 46 85 47 48 49 51 50 52 8 20 53 55 54 56 57 58 59 2 60 2 61 9 62 63 67 69 21 68 70 24 71 72 25 74 10 73 75 23 76 77 11 22 78 79 12 80 13 84 81 82 83 Figure 11. Consensus Bayesian topology of trees sampled from the posterior distribution (at stationarity) of 86 representative taxa from Hunt et al. 2007. The values above nodes indicate posterior probabilities. The values below nodes indicate clade number (refer to Table 2 for ancestral state reconstruction likelihood values for each node). 467 CHRYSOPIDAE Chrysoperla carnea SIALIDAE Sialis lutaria RAPHIDIIDAE Phaeostigma notata Priacma serrata ARCHOSTEMATA ARCHOSTEMATA Hydroscapha natans MYXOPHAGA MYXOPHAGA Gyrinus sp. Macrogyrus sp. GYRINIDAE Patrus sp. Dytiscus sp. DYTISCIDAE HYDRADEPHAGA Hydroporus sp. Haliplus sp. HALIPLIDAE Euryderus grossus Clinidium sp. -
Mckenna2009chap34.Pdf
Beetles (Coleoptera) Duane D. McKenna* and Brian D. Farrell and Polyphaga (~315,000 species; checkered beetles, Department of Organismic and Evolutionary Biology, 26 Oxford click beetles, A reP ies, ladybird beetles, leaf beetles, long- Street, Harvard University, Cambridge, MA 02138, USA horn beetles, metallic wood-boring beetles, rove beetles, *To whom correspondence should be addressed scarabs, soldier beetles, weevils, and others) (2, 3). 7 e ([email protected]) most recent higher-level classiA cation for living beetles recognizes 16 superfamilies and 168 families (4, 5). Abstract Members of the Suborder Adephaga are largely preda- tors, Archostemata feed on decaying wood (larvae) and Beetles are placed in the insect Order Coleoptera (~350,000 pollen (adults), and Myxophaga are aquatic or semi- described species). Recent molecular phylogenetic stud- aquatic and feed on green and/or blue-green algae ( 6). ies defi ne two major groups: (i) the Suborders Myxophaga Polyphaga exhibit a diversity of habits, but most spe- and Archostemata, and (ii) the Suborders Adephaga and cies feed on plants or dead and decaying plant parts Polyphaga. The time of divergence of these groups has (1–3). 7 e earliest known fossil Archostemata are from been estimated with molecular clocks as ~285–266 million the late Permian (7), and the earliest unequivocal fossil years ago (Ma), with the Adephaga–Polyphaga split at ~277– Adephaga and Polyphaga are from the early Triassic (1). 266 Ma. A majority of the more than 160 beetle families Myxophaga are not known from the fossil record, but are estimated to have originated in the Jurassic (200–146 extinct possible relatives are known from the Permian Ma). -
Logs and Chips of Eighteen Eucalypt Species from Australia
United States Department of Agriculture Pest Risk Assessment Forest Service of the Importation Into Forest Products Laboratory the United States of General Technical Report Unprocessed Logs and FPL−GTR−137 Chips of Eighteen Eucalypt Species From Australia P. (=Tryphocaria) solida, P. tricuspis; Scolecobrotus westwoodi; Abstract Tessaromma undatum; Zygocera canosa], ghost moths and carpen- The unmitigated pest risk potential for the importation of unproc- terworms [Abantiades latipennis; Aenetus eximius, A. ligniveren, essed logs and chips of 18 species of eucalypts (Eucalyptus amyg- A. paradiseus; Zelotypia stacyi; Endoxyla cinereus (=Xyleutes dalina, E. cloeziana, E. delegatensis, E. diversicolor, E. dunnii, boisduvali), Endoxyla spp. (=Xyleutes spp.)], true powderpost E. globulus, E. grandis, E. nitens, E. obliqua, E. ovata, E. pilularis, beetles (Lyctus brunneus, L. costatus, L. discedens, L. parallelocol- E. regnans, E. saligna, E. sieberi, E. viminalis, Corymbia calo- lis; Minthea rugicollis), false powderpost or auger beetles (Bo- phylla, C. citriodora, and C. maculata) from Australia into the strychopsis jesuita; Mesoxylion collaris; Sinoxylon anale; Xylion United States was assessed by estimating the likelihood and conse- cylindricus; Xylobosca bispinosa; Xylodeleis obsipa, Xylopsocus quences of introduction of representative insects and pathogens of gibbicollis; Xylothrips religiosus; Xylotillus lindi), dampwood concern. Twenty-two individual pest risk assessments were pre- termite (Porotermes adamsoni), giant termite (Mastotermes dar- pared, fifteen dealing with insects and seven with pathogens. The winiensis), drywood termites (Neotermes insularis; Kalotermes selected organisms were representative examples of insects and rufinotum, K. banksiae; Ceratokalotermes spoliator; Glyptotermes pathogens found on foliage, on the bark, in the bark, and in the tuberculatus; Bifiditermes condonensis; Cryptotermes primus, wood of eucalypts. C. -
The Beetles of Decaying Wood in Ireland
The beetles of decaying wood in Ireland. A provisional annotated checklist of saproxylic Coleoptera. Irish Wildlife Manuals No. 65 The beetles of decaying wood in Ireland. A provisional annotated checklist of saproxylic Coleoptera. Keith N. A. Alexander 1 & Roy Anderson 2 1 59 Sweetbrier Lane, Heavitree, Exeter EX1 3AQ; 2 1 Belvoirview Park, Belfast BT8 7BL, N. Ireland Citation : Alexander, K. N. A. & Anderson, R. (2012) The beetles of decaying wood in Ireland. A provisional annotated checklist of saproxylic Coleoptera. Irish Wildlife Manual s, No. 65. National Parks and Wildlife Service, Department of the Arts, Heritage and the Gaeltacht, Dublin, Ireland. Keywords: beetles; saproxylic; deadwood; timber; fungal decay; checklist Cover photo: The Rhinoceros Beetle, Sinodendron cylindricum © Roy Anderson The NPWS Project Officer for this report was: Dr Brian Nelson; [email protected] Irish Wildlife Manuals Series Editors: F. Marnell & N. Kingston © National Parks and Wildlife Service 2012 ISSN 1393 – 6670 Saproxylic beetles of Ireland ____________________________ Contents Executive Summary........................................................................................................................................ 2 Acknowledgements........................................................................................................................................2 Introduction....................................................................................................................................................