Zoochemical Screening and Antimicrobial Potential of Ground
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Arthropod Diversity and Conservation in Old-Growth Northwest Forests'
AMER. ZOOL., 33:578-587 (1993) Arthropod Diversity and Conservation in Old-Growth mon et al., 1990; Hz Northwest Forests complex litter layer 1973; Lattin, 1990; JOHN D. LATTIN and other features Systematic Entomology Laboratory, Department of Entomology, Oregon State University, tural diversity of th Corvallis, Oregon 97331-2907 is reflected by the 14 found there (Lawtt SYNOPSIS. Old-growth forests of the Pacific Northwest extend along the 1990; Parsons et a. e coastal region from southern Alaska to northern California and are com- While these old posed largely of conifer rather than hardwood tree species. Many of these ity over time and trees achieve great age (500-1,000 yr). Natural succession that follows product of sever: forest stand destruction normally takes over 100 years to reach the young through successioi mature forest stage. This succession may continue on into old-growth for (Lattin, 1990). Fire centuries. The changing structural complexity of the forest over time, and diseases, are combined with the many different plant species that characterize succes- bances. The prolot sion, results in an array of arthropod habitats. It is estimated that 6,000 a continually char arthropod species may be found in such forests—over 3,400 different ments and habitat species are known from a single 6,400 ha site in Oregon. Our knowledge (Southwood, 1977 of these species is still rudimentary and much additional work is needed Lawton, 1983). throughout this vast region. Many of these species play critical roles in arthropods have lx the dynamics of forest ecosystems. They are important in nutrient cycling, old-growth site, tt as herbivores, as natural predators and parasites of other arthropod spe- mental Forest (HJ cies. -
Mitochondrial Genomes Resolve the Phylogeny of Adephaga
1 Mitochondrial genomes resolve the phylogeny 2 of Adephaga (Coleoptera) and confirm tiger 3 beetles (Cicindelidae) as an independent family 4 Alejandro López-López1,2,3 and Alfried P. Vogler1,2 5 1: Department of Life Sciences, Natural History Museum, London SW7 5BD, UK 6 2: Department of Life Sciences, Silwood Park Campus, Imperial College London, Ascot SL5 7PY, UK 7 3: Departamento de Zoología y Antropología Física, Facultad de Veterinaria, Universidad de Murcia, Campus 8 Mare Nostrum, 30100, Murcia, Spain 9 10 Corresponding author: Alejandro López-López ([email protected]) 11 12 Abstract 13 The beetle suborder Adephaga consists of several aquatic (‘Hydradephaga’) and terrestrial 14 (‘Geadephaga’) families whose relationships remain poorly known. In particular, the position 15 of Cicindelidae (tiger beetles) appears problematic, as recent studies have found them either 16 within the Hydradephaga based on mitogenomes, or together with several unlikely relatives 17 in Geadeadephaga based on 18S rRNA genes. We newly sequenced nine mitogenomes of 18 representatives of Cicindelidae and three ground beetles (Carabidae), and conducted 19 phylogenetic analyses together with 29 existing mitogenomes of Adephaga. Our results 20 support a basal split of Geadephaga and Hydradephaga, and reveal Cicindelidae, together 21 with Trachypachidae, as sister to all other Geadephaga, supporting their status as Family. We 22 show that alternative arrangements of basal adephagan relationships coincide with increased 23 rates of evolutionary change and with nucleotide compositional bias, but these confounding 24 factors were overcome by the CAT-Poisson model of PhyloBayes. The mitogenome + 18S 25 rRNA combined matrix supports the same topology only after removal of the hypervariable 26 expansion segments. -
Volume 28, No. 2, Fall 2009
Fall 2009 Vol. 28, No. 2 NEWSLETTER OF THE BIOLOGICAL SURVEY OF CANADA (TERRESTRIAL ARTHROPODS) Table of Contents General Information and Editorial Notes ..................................... (inside front cover) News and Notes News from the Biological Survey of Canada ..........................................................27 Report on the first AGM of the BSC .......................................................................27 Robert E. Roughley (1950-2009) ...........................................................................30 BSC Symposium at the 2009 JAM .........................................................................32 Demise of the NRC Research Press Monograph Series .......................................34 The Evolution of the BSC Newsletter .....................................................................34 The Alan and Anne Morgan Collection moves to Guelph ......................................34 Curation Blitz at Wallis Museum ............................................................................35 International Year of Biological Diversity 2010 ......................................................36 Project Update: Terrestrial Arthropods of Newfoundland and Labrador ..............37 Border Conflicts: How Leafhoppers Can Help Resolve Ecoregional Viewpoints 41 Project Update: Canadian Journal of Arthropod Identification .............................55 Arctic Corner The Birth of the University of Alaska Museum Insect Collection ............................57 Bylot Island and the Northern Biodiversity -
The Morphological Evolution of the Adephaga (Coleoptera)
Systematic Entomology (2019), DOI: 10.1111/syen.12403 The morphological evolution of the Adephaga (Coleoptera) ROLF GEORG BEUTEL1, IGNACIO RIBERA2 ,MARTIN FIKÁCEˇ K 3, ALEXANDROS VASILIKOPOULOS4, BERNHARD MISOF4 andMICHAEL BALKE5 1Institut für Zoologie und Evolutionsforschung, FSU Jena, Jena, Germany, 2Institut de Biología Evolutiva, CSIC-Universitat Pompeu Fabra, Barcelona, Spain, 3Department of Zoology, National Museum, Praha 9, Department of Zoology, Faculty of Science, Charles University, Praha 2, Czech Republic, 4Center for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, Bonn, Germany and 5Zoologische Staatssammlung, Munich, Germany Abstract. The evolution of the coleopteran suborder Adephaga is discussed based on a robust phylogenetic background. Analyses of morphological characters yield results nearly identical to recent molecular phylogenies, with the highly specialized Gyrinidae placed as sister to the remaining families, which form two large, reciprocally monophyletic subunits, the aquatic Haliplidae + Dytiscoidea (Meruidae, Noteridae, Aspidytidae, Amphizoidae, Hygrobiidae, Dytiscidae) on one hand, and the terrestrial Geadephaga (Trachypachidae + Carabidae) on the other. The ancestral habitat of Adephaga, either terrestrial or aquatic, remains ambiguous. The former option would imply two or three independent invasions of aquatic habitats, with very different structural adaptations in larvae of Gyrinidae, Haliplidae and Dytiscoidea. Introduction dedicated to their taxonomy (examples for comprehensive studies are Sharp, 1882; Guignot, 1931–1933; Balfour-Browne Adephaga, the second largest suborder of the megadiverse & Balfour-Browne, 1940; Jeannel, 1941–1942; Brinck, 1955, > Coleoptera, presently comprises 45 000 described species. Lindroth, 1961–1969; Franciscolo, 1979) and morphology. The terrestrial Carabidae are one of the largest beetle families, An outstanding contribution is the monograph on Dytiscus comprising almost 90% of the extant adephagan diversity. -
Carabidae Semiochemistry: Current and Future Directions
Journal of Chemical Ecology https://doi.org/10.1007/s10886-018-1011-8 REVIEW ARTICLE Carabidae Semiochemistry: Current and Future Directions Adam M. Rork1 & Tanya Renner1 Received: 30 May 2018 /Revised: 14 August 2018 /Accepted: 23 August 2018 # Springer Science+Business Media, LLC, part of Springer Nature 2018 Abstract Ground beetles (Carabidae) are recognized for their diverse, chemically-mediated defensive behaviors. Produced using a pair of pygidial glands, over 250 chemical constituents have been characterized across the family thus far, many of which are considered allomones. Over the past century, our knowledge of Carabidae exocrine chemistry has increased substantially, yet the role of these defensive compounds in mediating behavior other than repelling predators is largely unknown. It is also unclear whether non-defensive compounds produced by ground beetles mediate conspecific and heterospecific interactions, such as sex- aggregation pheromones or kairomones, respectively. Here we review the current state of non-exocrine Carabidae semiochemistry and behavioral research, discuss the importance of semiochemical research including but not limited to allomones, and describe next-generation methods for elucidating the underlying genetics and evolution of chemically- mediated behavior. Keywords Carabidae . Chemical ecology . Allomones . Entomology . Semiochemistry . Transcriptomics . Phylogenetics Introduction and behavioral research in Carabidae and discuss new methods for studying the underlying genetics and evolution Ground beetles (Carabidae) have long captured the attention of biosynthetic pathways responsible for synthesis of these of evolutionary biologists and chemical ecologists due to their semiochemicals. great diversity and array of chemical defensive strategies (Darwin 1846;Eisner1958). Since Thomas Eisner’s pioneering studies on bombardier beetles, knowledge of cara- Carabidae Semiochemistry bid defensive chemistry has grown tremendously, with over 250 distinct chemical classes currently described (Lečić et al. -
A Review of Myrmecophily in Ant Nest Beetles (Coleoptera: Carabidae: Paussinae): Linking Early Observations with Recent Findings
Naturwissenschaften (2007) 94:871–894 DOI 10.1007/s00114-007-0271-x REVIEW A review of myrmecophily in ant nest beetles (Coleoptera: Carabidae: Paussinae): linking early observations with recent findings Stefanie F. Geiselhardt & Klaus Peschke & Peter Nagel Received: 15 November 2005 /Revised: 28 February 2007 /Accepted: 9 May 2007 / Published online: 12 June 2007 # Springer-Verlag 2007 Abstract Myrmecophily provides various examples of as “bombardier beetles” is not used in contact with host how social structures can be overcome to exploit vast and ants. We attempt to trace the evolution of myrmecophily in well-protected resources. Ant nest beetles (Paussinae) are paussines by reviewing important aspects of the association particularly well suited for ecological and evolutionary between paussine beetles and ants, i.e. morphological and considerations in the context of association with ants potential chemical adaptations, life cycle, host specificity, because life habits within the subfamily range from free- alimentation, parasitism and sound production. living and predatory in basal taxa to obligatory myrme- cophily in derived Paussini. Adult Paussini are accepted in Keywords Evolution of myrmecophily. Paussinae . the ant society, although parasitising the colony by preying Mimicry. Ant parasites . Defensive secretion . on ant brood. Host species mainly belong to the ant families Host specificity Myrmicinae and Formicinae, but at least several paussine genera are not host-specific. Morphological adaptations, such as special glands and associated tufts of hair Introduction (trichomes), characterise Paussini as typical myrmecophiles and lead to two different strategical types of body shape: A great diversity of arthropods live together with ants and while certain Paussini rely on the protective type with less profit from ant societies being well-protected habitats with exposed extremities, other genera access ant colonies using stable microclimate (Hölldobler and Wilson 1990; Wasmann glandular secretions and trichomes (symphile type). -
This Work Is Licensed Under the Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License
This work is licensed under the Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/us/ or send a letter to Creative Commons, 171 Second Street, Suite 300, San Francisco, California, 94105, USA. Frontispiece. Photograph of habitus of Entomoantyx cyanipeimis (Chaudoir), dorsal aspect. Mexico, Veracruz, NE Catemaco, Los Tuxtlas Biological Station (CNCI). Standardized Body Length - 4.4 mm. THE MIDDLE AMERICAN GENERA OF THE TRIBE OZAENINI WITH NOTES ABOUT THE SPECIES IN SOUTHWESTERN UNITED STATES AND SELECTED SPECIES FROM MEXICO George E. Ball Department of Entomology University of Alberta Edmonton, Alberta Canada T6G 2E3 and Scott McCleve 2210 13th Street Douglas, Arizona Quaestiones Entomologicae 85607 U.S.A. 26: 30—116 ABSTRACT Based on structural features of adults, the following new taxa are described: Entomoantyx, new genus (type species— Ozaena cyanipennis Chaudoir, 1852); and Pachyteles (sensu stricto) enischnus, new species (type locality— Mexico, Jalisco, near Ixtapa). Combined in a single genus, but ranked as subgenera are: Pachyteles (s. str.j Perty, 1830 (type species— P. striola Perty, 1830); Goniotropis Gray, 1832 (type species— G. braziliensis Gray, 1832), with its junior synonym, Scythropasus Chaudoir, 1852 (type species— S. elongata Chaudoir, 1852); and Tropopsis Solier, 1849 (type species— T. marginicollis Solier, 1849). The following species-level synonymy is proposed, with the senior synonym and thus valid name listed first for each combination: Pachyteles (Goniotropis) parca LeConte, 1884 (type area— U.S.A., Arizona) = P. beyeri Notman, 1919 (type locality— Mexico, Baja California Norte, San Felipe); Pachyteles fs. -
Final Format
Forest Disturbance Effects on Insect and Bird Communities: Insectivorous Birds in Coast Live Oak Woodlands and Leaf Litter Arthropods in the Sierra Nevada by Kyle Owen Apigian B.A. (Bowdoin College) 1998 A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Environmental Science, Policy, and Management in the GRADUATE DIVISION of the UNIVERSITY OF CALIFORNIA, BERKELEY Committee in Charge: Professor Barbara Allen-Diaz, Chair Assistant Professor Scott Stephens Professor Wayne Sousa Spring 2005 The dissertation of Kyle Owen Apigian is approved: Chair Date Date Date University of California, Berkeley Spring 2005 Forest Disturbance Effects on Insect and Bird Communities: Insectivorous Birds in Coast Live Oak Woodlands and Leaf Litter Arthropods in the Sierra Nevada © 2005 by Kyle Owen Apigian TABLE OF CONTENTS Page List of Figures ii List of Tables iii Preface iv Acknowledgements Chapter 1: Foliar arthropod abundance in coast live oak (Quercus agrifolia) 1 woodlands: effects of tree species, seasonality, and “sudden oak death”. Chapter 2: Insectivorous birds change their foraging behavior in oak woodlands affected by Phytophthora ramorum (“sudden oak death”). Chapter 3: Cavity nesting birds in coast live oak (Quercus agrifolia) woodlands impacted by Phytophthora ramorum: use of artificial nest boxes and arthropod delivery to nestlings. Chapter 4: Biodiversity of Coleoptera and other leaf litter arthropods and the importance of habitat structural features in a Sierra Nevada mixed-conifer forest. Chapter 5: Fire and fire surrogate treatment effects on leaf litter arthropods in a western Sierra Nevada mixed-conifer forest. Conclusions References Appendices LIST OF FIGURES Page Chapter 1 Figure 1. -
From Plant Exploitation to Mutualism
From Plant Exploitation to Mutualism. Chapter 3 François Lieutier, Kalina Bermudez-Torres, James Cook, Marion O. Harris, Luc Legal, Aurélien Sallé, Bertrand Schatz, David Giron To cite this version: François Lieutier, Kalina Bermudez-Torres, James Cook, Marion O. Harris, Luc Legal, et al.. From Plant Exploitation to Mutualism. Chapter 3. Nicolas Sauvion, Denis Thiéry, Paul-André Calatayud. Insect-Plant Interactions in a Crop Protection Perspective, 81, 2017, Advances in Botanical Research, 978-0-12-803318-0. hal-02318872 HAL Id: hal-02318872 https://hal.archives-ouvertes.fr/hal-02318872 Submitted on 1 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. VOLUME EIGHTY ONE ADVANCES IN BOTANICAL RESEARCH Insect-Plant Interactions in a Crop Protection Perspective Volume Editor NICOLAS SAUVION INRA,UMR BGPI 0385 (INRA-CIRAD-SupAgro), Montpellier, France DENIS THIERY INRA, UMR SAVE 1065, Bordeaux Sciences Agro, Centre INRA de recherches de Bordeaux- Aquitaine, Institut des Sciences de la Vigne et du Vin, Villenave d’Ornon, France PAUL-ANDRE CALATAYUD IRD UMR EGCE (Evolution, Génome, Comportement, Ecologie), CNRS-IRD-Univ. Paris-Sud, IDEEV, Université Paris-Saclay, Gif-sur-Yvette, France; IRD c/o ICIPE, Nairobi, Kenya Academic Press is an imprint of Elsevier 125 London Wall, London EC2Y 5AS, United Kingdom The Boulevard, Langford Lane, Kidlington, Oxford OX5 1GB, United Kingdom 50 Hampshire Street, 5th Floor, Cambridge, MA 02139, United States 525 B Street, Suite 1800, San Diego, CA 92101-4495, United States First edition 2017 Copyright Ó 2017 Elsevier Ltd. -
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. -
BOTANICAL RESEARCH Insect-Plant Interactions in a Crop Protection Perspective ADVANCES in BOTANICAL RESEARCH
VOLUME EIGHTY ONE ADVANCES IN BOTANICAL RESEARCH Insect-Plant Interactions in a Crop Protection Perspective ADVANCES IN BOTANICAL RESEARCH Series Editors Jean-Pierre Jacquot Professor, Membre de L’Institut Universitaire de France, Unité Mixte de Recherche INRA, UHP 1136 “Interaction Arbres Microorganismes”, Université de Lorraine, Faculté des Sciences, Vandoeuvre, France Pierre Gadal Honorary Professor, Université Paris-Sud XI, Institut Biologie des Plantes, Orsay, France VOLUME EIGHTY ONE ADVANCES IN BOTANICAL RESEARCH Insect-Plant Interactions in a Crop Protection Perspective Volume Editor NICOLAS SAUVION INRA,UMR BGPI 0385 (INRA-CIRAD-SupAgro), Montpellier, France DENIS THIERY INRA, UMR SAVE 1065, Bordeaux Sciences Agro, Centre INRA de recherches de Bordeaux- Aquitaine, Institut des Sciences de la Vigne et du Vin, Villenave d’Ornon, France PAUL-ANDRE CALATAYUD IRD UMR EGCE (Evolution, Génome, Comportement, Ecologie), CNRS-IRD-Univ. Paris-Sud, IDEEV, Université Paris-Saclay, Gif-sur-Yvette, France; IRD c/o ICIPE, Nairobi, Kenya Academic Press is an imprint of Elsevier 125 London Wall, London EC2Y 5AS, United Kingdom The Boulevard, Langford Lane, Kidlington, Oxford OX5 1GB, United Kingdom 50 Hampshire Street, 5th Floor, Cambridge, MA 02139, United States 525 B Street, Suite 1800, San Diego, CA 92101-4495, United States First edition 2017 Copyright Ó 2017 Elsevier Ltd. All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the publisher. Details on how to seek permission, further information about the Publisher’s permissions policies and our arrangements with organizations such as the Copyright Clearance Center and the Copyright Licensing Agency, can be found at our website: www.elsevier.com/permissions. -
~~- ~~ 7.8. Carabidae Latreille, 1802
Carabidae Latreille, 1802 119 ~ ~/.A' .~..A ---:: o,,~ ~~~ ~ ~~- ~~ I ~ A B Fig. 7.7.4. Larval head structures. A, nasale and adnasalia, Systolosoma lateritium, S. breve, Trachypachus IlOlmbergi; B, antennae, S. lateritium, T.holmbergi;C- E, S. lateritium.C, mandible; D, maxilla, E, labium; F- H, tergite IX. F. S. lateri- tium; G, T. holmbergi; H, S. breve. From Beutel & Arndt (1995), redrawn. morphies (Arndt & Beutel 1995): sensorial ap- Hlavac, T. F. (1975): The prothorax of Coleoptera (ex- pendage on lateral side of antennomere III ab- cept Bostrichiformia - Cucujiformia). - Bulletin sent, replaced by ventral sensorial field, apical of the Museum of Comparative Zoology 147 (4): 137-183. part of maxillary palpomere 3 with additional se- tae, number of nasal teeth increased (6-8), uro- Lindroth, C. H. (1960): The larva of Trachypachus Mtsch., Gehringia Darl., and Opisthius Kirby (Col. gomphi fixed, horn-shaped (groundplan), eight Carabidae). - OpusculaEntomologica25: 30-42. long setae on tergite IX (including those on uro- (1961- 69): The ground beetles (Carabidae, excl. gomphi). The specific shape of the parameres Cicindelinae) of Canada and Alaska. Parts 1-6. - (Lindroth 1961-69; Beutel 1994) is an autapo- Opuscula Entomologica XlVIII + 1192 pp. 1961, morphy of adults. The absence of the katas- Part 2, Suppl. 20: 1- 20; 1963, Part 3, Suppl. 24: tigma, the specific sculpture of the elytra, the 201-408; 1966, Part 4, Suppl. 29: 409-648; 1968, kidney-shaped sensorial field of the larval anten- Part 5, Suppl. 33: 649-944; 1969 Part 6, Suppl. 34: nomere 3 and the large, ventral sensorial field 945-1192; 1969 Part I, Suppl.