Forestry in a Changing World: New Challenges and Opportunities
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Diptera: Calyptratae)
Systematic Entomology (2020), DOI: 10.1111/syen.12443 Protein-encoding ultraconserved elements provide a new phylogenomic perspective of Oestroidea flies (Diptera: Calyptratae) ELIANA BUENAVENTURA1,2 , MICHAEL W. LLOYD2,3,JUAN MANUEL PERILLALÓPEZ4, VANESSA L. GONZÁLEZ2, ARIANNA THOMAS-CABIANCA5 andTORSTEN DIKOW2 1Museum für Naturkunde, Leibniz Institute for Evolution and Biodiversity Science, Berlin, Germany, 2National Museum of Natural History, Smithsonian Institution, Washington, DC, U.S.A., 3The Jackson Laboratory, Bar Harbor, ME, U.S.A., 4Department of Biological Sciences, Wright State University, Dayton, OH, U.S.A. and 5Department of Environmental Science and Natural Resources, University of Alicante, Alicante, Spain Abstract. The diverse superfamily Oestroidea with more than 15 000 known species includes among others blow flies, flesh flies, bot flies and the diverse tachinid flies. Oestroidea exhibit strikingly divergent morphological and ecological traits, but even with a variety of data sources and inferences there is no consensus on the relationships among major Oestroidea lineages. Phylogenomic inferences derived from targeted enrichment of ultraconserved elements or UCEs have emerged as a promising method for resolving difficult phylogenetic problems at varying timescales. To reconstruct phylogenetic relationships among families of Oestroidea, we obtained UCE loci exclusively derived from the transcribed portion of the genome, making them suitable for larger and more integrative phylogenomic studies using other genomic and transcriptomic resources. We analysed datasets containing 37–2077 UCE loci from 98 representatives of all oestroid families (except Ulurumyiidae and Mystacinobiidae) and seven calyptrate outgroups, with a total concatenated aligned length between 10 and 550 Mb. About 35% of the sampled taxa consisted of museum specimens (2–92 years old), of which 85% resulted in successful UCE enrichment. -
Entomology 101 Jason J
Entomology 101 Jason J. Dombroskie Manager, Cornell U. Insect Collection Coordinator, Insect Diagnostic Lab This material [email protected] can only be used for CCE MGV audiences. Outline • What is an insect? • Anatomy • Life cycles • Diversity • Major orders • Herbivory Corydalus cornutus Cornell U. Insect Collection • > 7 million specimens • ~200 000 species • worldwide coverage • http://cuic.entomology.cornell.edu/ • on facebook Insect Diagnostic Lab • ~700 IDs per year • 10-20 000 IDs for NYS Dept. Ag. & Markets • occasionally IDs can be made from a photo • mostly local, but some submissions worldwide • $25 fee • http://entomology.cornell.edu/IDL Arthropods Regier, et al. 2005 What is an insect? • 3 main body parts • 6 jointed legs • 1 pair of antennae • compound eyes • usually some sort of metamorphosis Booneacris glacialis Head • antennae • mouthparts • compound eyes • ocelli Monochamus scutellatus Popillia japonica Tetanocera sp. Antheraea polyphemus wikimedia commons labrum maxilla mandible labium Corydalus cornutus Polygonia progne Aedes sp. Hybomitra zonalis Monochamus notatus Aeshna canadensis Isoptera Darapsa myron Thorax • six legs • four wings or less • muscular Amateur Entomologists’ Society Entomologists’ Amateur Limenitis archippus Lethocerus americanus Zeugomantispa minuta Machimus sp. with Herpetogramma pertextalis wikimedia commons Tipula apicalis Cybister fimbriolatus Elasmucha lateralis Automeris io Abdomen • internal organs • genitalia • ovipositor Ophiogomphus rupinsulensis Lauxania shewelli Merope tuber Adoxophyes -
Maternal Care in Acanthosomatinae (Insecta: Heteroptera: Acanthosomatidae)̶Correlated Evolution with Title Morphological Change
Maternal care in Acanthosomatinae (Insecta: Heteroptera: Acanthosomatidae)̶correlated evolution with Title morphological change Author(s) Tsai, Jing-Fu; Kudo, Shin-ichi; Yoshizawa, Kazunori BMC Evolutionary Biology, 15, 258 Citation https://doi.org/10.1186/s12862-015-0537-4 Issue Date 2015-11-19 Doc URL http://hdl.handle.net/2115/63251 Rights(URL) http://creativecommons.org/licenses/by/4.0 Type article File Information 10.1186_s12862-015-0537-4.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Tsai et al. BMC Evolutionary Biology (2015) 15:258 DOI 10.1186/s12862-015-0537-4 RESEARCH ARTICLE Open Access Maternal care in Acanthosomatinae (Insecta: Heteroptera: Acanthosomatidae)— correlated evolution with morphological change Jing-Fu Tsai1,3*, Shin-ichi Kudo2 and Kazunori Yoshizawa1 Abstract Background: Maternal care (egg-nymph guarding behavior) has been recorded in some genera of Acanthosomatidae. However, the origin of the maternal care in the family has remained unclear due to the lack of phylogenetic hypotheses. Another reproductive mode is found in non-caring species whose females smear their eggs before leaving them. They possess pairs of complex organs on the abdominal venter called Pendergrast’s organ (PO) and spread the secretion of this organ onto each egg with their hind legs, which is supposed to provide a protective function against enemies. Some authors claim that the absence of PO may be associated with the presence of maternal care. No study, however, has tested this hypothesis of a correlated evolution between the two traits. Results: We reconstructed the molecular phylogeny of the subfamily Acanthosomatinae using five genetic markers sequenced from 44 species and one subspecies with and without maternal care. -
Arachnids (Excluding Acarina and Pseudoscorpionida) of the Wichita Mountains Wildlife Refuge, Oklahoma
OCCASIONAL PAPERS THE MUSEUM TEXAS TECH UNIVERSITY NUMBER 67 5 SEPTEMBER 1980 ARACHNIDS (EXCLUDING ACARINA AND PSEUDOSCORPIONIDA) OF THE WICHITA MOUNTAINS WILDLIFE REFUGE, OKLAHOMA JAMES C. COKENDOLPHER AND FRANK D. BRYCE The Wichita Mountains are located in eastern Greer, southern Kiowa, and northwestern Comanche counties in Oklahoma. Since their formation more than 300 million years ago, these rugged mountains have been fragmented and weathered, until today the highest peak (Mount Pinchot) stands only 756 meters above sea level (Tyler, 1977). The mountains are composed predominantly of granite and gabbro. Forests of oak, elm, and walnut border most waterways, while at elevations from 153 to 427 meters prair ies are the predominant vegetation type. A more detailed sum mary of the climatic and biotic features of the Wichitas has been presented by Blair and Hubbell (1938). A large tract of land in the eastern range of the Wichita Moun tains (now northeastern Comanche County) was set aside as the Wichita National Forest by President McKinley during 1901. In 1905, President Theodore Roosevelt created a game preserve on those lands managed by the Forest Service. Since 1935, this pre serve has been known as the Wichita Mountains Wildlife Refuge. Numerous papers on Oklahoma spiders have been published (Bailey and Chada, 1968; Bailey et al., 1968; Banks et al, 1932; Branson, 1958, 1959, 1966, 1968; Branson and Drew, 1972; Gro- thaus, 1968; Harrel, 1962, 1965; Horner, 1975; Rogers and Horner, 1977), but only a single, comprehensive work (Banks et al., 1932) exists covering all arachnid orders in the state. Further additions and annotations to the arachnid fauna of Oklahoma can be found 2 OCCASIONAL PAPERS MUSEUM TEXAS TECH UNIVERSITY in recent revisionary studies. -
Sexual Selection Research on Spiders: Progress and Biases
Biol. Rev. (2005), 80, pp. 363–385. f Cambridge Philosophical Society 363 doi:10.1017/S1464793104006700 Printed in the United Kingdom Sexual selection research on spiders: progress and biases Bernhard A. Huber* Zoological Research Institute and Museum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany (Received 7 June 2004; revised 25 November 2004; accepted 29 November 2004) ABSTRACT The renaissance of interest in sexual selection during the last decades has fuelled an extraordinary increase of scientific papers on the subject in spiders. Research has focused both on the process of sexual selection itself, for example on the signals and various modalities involved, and on the patterns, that is the outcome of mate choice and competition depending on certain parameters. Sexual selection has most clearly been demonstrated in cases involving visual and acoustical signals but most spiders are myopic and mute, relying rather on vibrations, chemical and tactile stimuli. This review argues that research has been biased towards modalities that are relatively easily accessible to the human observer. Circumstantial and comparative evidence indicates that sexual selection working via substrate-borne vibrations and tactile as well as chemical stimuli may be common and widespread in spiders. Pattern-oriented research has focused on several phenomena for which spiders offer excellent model objects, like sexual size dimorphism, nuptial feeding, sexual cannibalism, and sperm competition. The accumulating evidence argues for a highly complex set of explanations for seemingly uniform patterns like size dimorphism and sexual cannibalism. Sexual selection appears involved as well as natural selection and mechanisms that are adaptive in other contexts only. Sperm competition has resulted in a plethora of morpho- logical and behavioural adaptations, and simplistic models like those linking reproductive morphology with behaviour and sperm priority patterns in a straightforward way are being replaced by complex models involving an array of parameters. -
Morphology, Taxonomy, and Biology of Larval Scarabaeoidea
Digitized by the Internet Archive in 2011 with funding from University of Illinois Urbana-Champaign http://www.archive.org/details/morphologytaxono12haye ' / ILLINOIS BIOLOGICAL MONOGRAPHS Volume XII PUBLISHED BY THE UNIVERSITY OF ILLINOIS *, URBANA, ILLINOIS I EDITORIAL COMMITTEE John Theodore Buchholz Fred Wilbur Tanner Charles Zeleny, Chairman S70.S~ XLL '• / IL cop TABLE OF CONTENTS Nos. Pages 1. Morphological Studies of the Genus Cercospora. By Wilhelm Gerhard Solheim 1 2. Morphology, Taxonomy, and Biology of Larval Scarabaeoidea. By William Patrick Hayes 85 3. Sawflies of the Sub-family Dolerinae of America North of Mexico. By Herbert H. Ross 205 4. A Study of Fresh-water Plankton Communities. By Samuel Eddy 321 LIBRARY OF THE UNIVERSITY OF ILLINOIS ILLINOIS BIOLOGICAL MONOGRAPHS Vol. XII April, 1929 No. 2 Editorial Committee Stephen Alfred Forbes Fred Wilbur Tanner Henry Baldwin Ward Published by the University of Illinois under the auspices of the graduate school Distributed June 18. 1930 MORPHOLOGY, TAXONOMY, AND BIOLOGY OF LARVAL SCARABAEOIDEA WITH FIFTEEN PLATES BY WILLIAM PATRICK HAYES Associate Professor of Entomology in the University of Illinois Contribution No. 137 from the Entomological Laboratories of the University of Illinois . T U .V- TABLE OF CONTENTS 7 Introduction Q Economic importance Historical review 11 Taxonomic literature 12 Biological and ecological literature Materials and methods 1%i Acknowledgments Morphology ]* 1 ' The head and its appendages Antennae. 18 Clypeus and labrum ™ 22 EpipharynxEpipharyru Mandibles. Maxillae 37 Hypopharynx <w Labium 40 Thorax and abdomen 40 Segmentation « 41 Setation Radula 41 42 Legs £ Spiracles 43 Anal orifice 44 Organs of stridulation 47 Postembryonic development and biology of the Scarabaeidae Eggs f*' Oviposition preferences 48 Description and length of egg stage 48 Egg burster and hatching Larval development Molting 50 Postembryonic changes ^4 54 Food habits 58 Relative abundance. -
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 -
The Planthopper Genus <I>Acanalonia </I>In the United
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida September 1995 The planthopper genus Acanalonia in the United States (Homoptera: Issidae): male and female genitalic morphology Rebecca Freund University of South Dakota, Vermillion, SD Stephen W. Wilson Central Missouri State University, Warrensburg, MO Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Freund, Rebecca and Wilson, Stephen W., "The planthopper genus Acanalonia in the United States (Homoptera: Issidae): male and female genitalic morphology" (1995). Insecta Mundi. 133. https://digitalcommons.unl.edu/insectamundi/133 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI, Vol. 9, No. 3-4, September - December, 1995 195 The planthopper genus Acanalonia in the United States (Homoptera: Issidae): male and female genitalic morphology Rebecca Freund Department of Biology, University of South Dakota, Vermillion, SD 57069 and Stephen W. Wilson Department of Biology, Central Missouri State University, Warrensburg, MO 64093 Abstract: The issidplanthopper genus Acanalonia is reviewed anda key to the 18 speciesprovided. Detailed descriptions and illustrationsof the complete external morphology ofA. conica (Say), anddescriptionsandillustrationsof the male and female external genitalia ofthe species ofunited States Acanalonia are given. The principal genitalic features usedto separate species included: male - shape andlength ofthe aedeagalcaudal andlateralprocesses, and presence ofcaudalextensions; female -shape ofthe 8th abdominal segment and the number of teeth on the gonapophysis ofthe 8th segment. -
Universidade Federal Do Recôncavo Da Bahia Centro De Ciências Agrárias, Ambientais E Biológicas
UNIVERSIDADE FEDERAL DO RECÔNCAVO DA BAHIA CENTRO DE CIÊNCIAS AGRÁRIAS, AMBIENTAIS E BIOLÓGICAS ANÁLISE ACÚSTICA E MORFOLÓGICA DE TRÊS ESPÉCIES DE NEMOBIINAE (ORTHOPTERA: GRYLLOIDEA: TRIGONIDIIDAE) DO PANTANAL NORTE, MATO GROSSO, BRASIL LARISSA FREITAS DE MELO Bacharela em Biologia CRUZ DAS ALMAS BAHIA - BRASIL 2018 i LARISSA FREITAS DE MELO ANÁLISE ACÚSTICA E MORFOLÓGICA DE TRÊS ESPÉCIES DE NEMOBIINAE (ORTHOPTERA: GRYLLOIDEA: TRIGONIDIIDAE) DO PANTANAL NORTE, MATO GROSSO, BRASIL Trabalho de Conclusão de Curso apresentado à Universidade Federal do Recôncavo da Bahia, como parte dos requisitos do Curso de Graduação de Bacharelado em Biologia, para obtenção do título de Bacharel em Biologia. CRUZ DAS ALMAS BAHIA - BRASIL 2018 ii iii Dedico à minha amada família, essenciais em minha vida. iv AGRADECIMENTOS Meus mais profundos agradecimentos a cada ser de luz que esteve ao meu lado nesta tão longa e árdua jornada, vibrando e torcendo pelo meu sucesso e a cada conquista alcançada. Agradeço primeiramente ao meu maior guia Deus, aquele que permaneceu ao meu lado em todos os momentos, fossem eles bons ou ruins, me permitindo seguir sempre em frente com fé, sabedoria e paciência e que me oferece a força necessária para superar qualquer obstáculo, muitíssimo obrigada. À Universidade Federal do Recôncavo da Bahia, instituição que me permitiu crescer profissionalmente, dando suporte necessário e possibilitando que eu tivesse os melhores docentes para o curso de Bacharelado em Biologia. Ao Laboratório de Ecologia e Taxonomia de Insetos (LETI), onde eu pude aprender sobre o maravilhoso mundo dos insetos e onde pude conhecer pessoas especiais que me fizeram rir muito e pela troca de conhecimento entre nós. -
Comparison of Coleoptera Emergent from Various Decay Classes of Downed Coarse Woody Debris in Great Smoky Mountains National Park, USA
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 11-30-2012 Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains National Park, USA Michael L. Ferro Louisiana State Arthropod Museum, [email protected] Matthew L. Gimmel Louisiana State University AgCenter, [email protected] Kyle E. Harms Louisiana State University, [email protected] Christopher E. Carlton Louisiana State University Agricultural Center, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Ferro, Michael L.; Gimmel, Matthew L.; Harms, Kyle E.; and Carlton, Christopher E., "Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains National Park, USA" (2012). Insecta Mundi. 773. https://digitalcommons.unl.edu/insectamundi/773 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA A Journal of World Insect Systematics MUNDI 0260 Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains Na- tional Park, USA Michael L. Ferro Louisiana State Arthropod Museum, Department of Entomology Louisiana State University Agricultural Center 402 Life Sciences Building Baton Rouge, LA, 70803, U.S.A. [email protected] Matthew L. Gimmel Division of Entomology Department of Ecology & Evolutionary Biology University of Kansas 1501 Crestline Drive, Suite 140 Lawrence, KS, 66045, U.S.A. -
Insects of Larose Forest (Excluding Lepidoptera and Odonates)
Insects of Larose Forest (Excluding Lepidoptera and Odonates) • Non-native species indicated by an asterisk* • Species in red are new for the region EPHEMEROPTERA Mayflies Baetidae Small Minnow Mayflies Baetidae sp. Small minnow mayfly Caenidae Small Squaregills Caenidae sp. Small squaregill Ephemerellidae Spiny Crawlers Ephemerellidae sp. Spiny crawler Heptageniiidae Flatheaded Mayflies Heptageniidae sp. Flatheaded mayfly Leptophlebiidae Pronggills Leptophlebiidae sp. Pronggill PLECOPTERA Stoneflies Perlodidae Perlodid Stoneflies Perlodid sp. Perlodid stonefly ORTHOPTERA Grasshoppers, Crickets and Katydids Gryllidae Crickets Gryllus pennsylvanicus Field cricket Oecanthus sp. Tree cricket Tettigoniidae Katydids Amblycorypha oblongifolia Angular-winged katydid Conocephalus nigropleurum Black-sided meadow katydid Microcentrum sp. Leaf katydid Scudderia sp. Bush katydid HEMIPTERA True Bugs Acanthosomatidae Parent Bugs Elasmostethus cruciatus Red-crossed stink bug Elasmucha lateralis Parent bug Alydidae Broad-headed Bugs Alydus sp. Broad-headed bug Protenor sp. Broad-headed bug Aphididae Aphids Aphis nerii Oleander aphid* Paraprociphilus tesselatus Woolly alder aphid Cicadidae Cicadas Tibicen sp. Cicada Cicadellidae Leafhoppers Cicadellidae sp. Leafhopper Coelidia olitoria Leafhopper Cuernia striata Leahopper Draeculacephala zeae Leafhopper Graphocephala coccinea Leafhopper Idiodonus kelmcottii Leafhopper Neokolla hieroglyphica Leafhopper 1 Penthimia americana Leafhopper Tylozygus bifidus Leafhopper Cercopidae Spittlebugs Aphrophora cribrata -
East Fork Illinois River Channel and Floodplain Restoration Project Wildlife BE and Specialist Report
United States Department of Agriculture Forest Service East Fork Illinois River Channel and Floodplain Restoration Project Wildlife BE and Specialist Report Wild Rivers Ranger District, Rogue River – Siskiyou National Forest, Josephine County, OR Prepared By: /s/ Bonnie Allison February 27, 2015 Bonnie Allison, Zone Wildlife Biologist Wild Rivers and Siskiyou Mountains Ranger Districts Contents Contents ............................................................................................................................................ i Introduction ..................................................................................................................................... 1 Proposed Project Location .......................................................................................................... 1 Purpose and Need ........................................................................................................................ 2 Action Alternatives ..................................................................................................................... 3 Regulatory Setting ........................................................................................................................... 4 Forest Plan Management Direction ............................................................................................. 4 ESA Consultation to Date ........................................................................................................... 5 Other Relevant Laws, Policies and Regulations