A Re-Analysis of the Data in Sharkey Et Al.'S (2021) Minimalist Revision Reveals That Bins Do Not Deserve Names, but BOLD Syst
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Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(S): Diego J
Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(s): Diego J. Inclan and John O. Stireman, III Source: Annals of the Entomological Society of America, 104(2):287-296. Published By: Entomological Society of America https://doi.org/10.1603/AN10047 URL: http://www.bioone.org/doi/full/10.1603/AN10047 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. CONSERVATION BIOLOGY AND BIODIVERSITY Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States 1 DIEGO J. INCLAN AND JOHN O. STIREMAN, III Department of Biological Sciences, 3640 Colonel Glenn Highway, 235A, BH, Wright State University, Dayton, OH 45435 Ann. Entomol. Soc. Am. 104(2): 287Ð296 (2011); DOI: 10.1603/AN10047 ABSTRACT Although tachinids are one of the most diverse families of Diptera and represent the largest group of nonhymenopteran parasitoids, their local diversity and distribution patterns of most species in the family are poorly known. -
To Us Insectometers, It Is Clear That Insect Decline in Our Costa Rican
SPECIAL FEATURE: PERSPECTIVE To us insectometers, it is clear that insect decline in our Costa Rican tropics is real, so let’sbekindto SPECIAL FEATURE: PERSPECTIVE the survivors Daniel H. Janzena,1 and Winnie Hallwachsa Edited by David L. Wagner, University of Connecticut, and accepted by Editorial Board Member May R. Berenbaum November 11, 2020 (received for review April 6, 2020) We have been field observers of tropical insects on four continents and, since 1978, intense observers of caterpillars, their parasites, and their associates in the 1,260 km2 of dry, cloud, and rain forests of Area´ de Conservaci ´onGuanacaste (ACG) in northwestern Costa Rica. ACG’s natural ecosystem restoration began with its national park designation in 1971. As human biomonitors, or “insectometers,” we see that ACG’s insect species richness and density have gradually declined since the late 1970s, and more intensely since about 2005. The overarching perturbation is climate change. It has caused increasing ambient tempera- tures for all ecosystems; more erratic seasonal cues; reduced, erratic, and asynchronous rainfall; heated air masses sliding up the volcanoes and burning off the cloud forest; and dwindling biodiversity in all ACG terrestrial ecosystems. What then is the next step as climate change descends on ACG’s many small-scale successes in sustainable biodevelopment? Be kind to the survivors by stimulating and facilitating their owner societies to value them as legitimate members of a green sustainable nation. Encourage national bioliteracy, BioAlfa. climate change | BioAlfa | conservation by rewilding | biodevelopment | insect decline As “insectometers,” also known as human biomoni- eventually focused into Area´ de Conservaci ´onGuana- tors, we have watched the conspicuous ongoing de- caste (ACG) in northwestern Costa Rica (8–13) (Fig. -
Diptera: Tachinidae), from Area De Conservación Guanacaste, Northwestern Costa Rica, with a Key for Their Identification
Biodiversity Data Journal 3: e4595 doi: 10.3897/BDJ.3.e4595 Taxonomic Paper Three new species of Trigonospila Pokorny (Diptera: Tachinidae), from Area de Conservación Guanacaste, northwestern Costa Rica, with a key for their identification AJ Fleming‡‡, D. Monty Wood , Daniel H Janzen§, Winnie Hallwachs§, M. Alex Smith | ‡ Agriculture Agri-Food Canada, Ottawa, Canada § University of Pennsylvania, Philadelphia, PA, United States of America | Department of Integrative Biology, Guelph, Canada Corresponding author: AJ Fleming ([email protected]) Academic editor: Pierfilippo Cerretti Received: 26 Jan 2015 | Accepted: 07 Aug 2015 | Published: 11 Aug 2015 Citation: Fleming A, Wood D, Janzen D, Hallwachs W, Smith M (2015) Three new species of Trigonospila Pokorny (Diptera: Tachinidae), from Area de Conservación Guanacaste, northwestern Costa Rica, with a key for their identification. Biodiversity Data Journal 3: e4595. doi: 10.3897/BDJ.3.e4595 ZooBank: urn:lsid:zoobank.org:pub:E334B70E-8CD1-4E4A-9E00-08F77A36F178 Abstract We describe three new species of Trigonospila Pokorny (Tachinidae: Blondeliini) from Area de Conservación Guanacaste (ACG), northwestern Costa Rica. All were reared from various species of ACG caterpillars during an ongoing inventory of caterpillars, their food plants and their parasitoids in dry forest, rain forest and cloud forest. By coupling morphology, photographic documentation, life history and molecular data, we provide a clear and concise description of each species. All species published as new, are known to be previously undescribed as a result of careful study of the genus by DMW. This study builds on the current knowledge of the genus by adding three new species to the current 7 described in the New World. -
A Re-Analysis of the Data in Sharkey Et Al.'S (2021) Minimalist Revision
bioRxiv preprint doi: https://doi.org/10.1101/2021.04.28.441626; this version posted April 29, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. A re-analysis of the data in Sharkey et al.’s (2021) minimalist revision reveals that BINs do not deserve names, but BOLD Systems needs a stronger commitment to open science Rudolf Meier1,2, Bonny Blaimer2, Eliana Buenaventura2, Emily Hartop3,4, Thomas von Rintelen2, Amrita Srivathsan1, Darren Yeo1 1 Department of Biological Sciences, National University of Singapore, Singapore 2 Museum für Naturkunde, Leibniz Institute for Evolution and Biodiversity Science, Center for Integrative Biodiversity Discovery, Berlin, Germany 3 Zoology Department, Stockholms Universitet, Stockholm, Sweden 4 Station Linné, Öland, Sweden bioRxiv preprint doi: https://doi.org/10.1101/2021.04.28.441626; this version posted April 29, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract Halting biodiversity decline is one of the most critical challenges for humanity, but biodiversity assessment and monitoring are hampered by taxonomic impediments. We here distinguish between a “dark taxon impediment” caused by a large number of undescribed species and a “superficial description impediment” caused by species descriptions so imprecise that type specimens have to be consulted in order to resolve species identities. -
Extreme Diversity of Tropical Parasitoid Wasps Exposed by Iterative Integration of Natural History, DNA Barcoding, Morphology, and Collections
Extreme diversity of tropical parasitoid wasps exposed by iterative integration of natural history, DNA barcoding, morphology, and collections M. Alex Smith*†, Josephine J. Rodriguez‡, James B. Whitfield‡, Andrew R. Deans§, Daniel H. Janzen†¶, Winnie Hallwachs¶, and Paul D. N. Hebert* *The Biodiversity Institute of Ontario, University of Guelph, Guelph Ontario, N1G 2W1 Canada; ‡Department of Entomology, 320 Morrill Hall, University of Illinois, 505 S. Goodwin Avenue, Urbana, IL 61801; §Department of Entomology, North Carolina State University, Campus Box 7613, 2301 Gardner Hall, Raleigh, NC 27695-7613; and ¶Department of Biology, University of Pennsylvania, Philadelphia, PA 19104-6018 Contributed by Daniel H. Janzen, May 31, 2008 (sent for review April 18, 2008) We DNA barcoded 2,597 parasitoid wasps belonging to 6 microgas- A detailed recognition of species in parasitoid communities is trine braconid genera reared from parapatric tropical dry forest, cloud necessary because of the pivotal role parasitoids play in food web forest, and rain forest in Area de Conservacio´ n Guanacaste (ACG) in structure and dynamics. While generalizations about the effects of northwestern Costa Rica and combined these data with records of parasitoids on community diversity are complex (7), a common- caterpillar hosts and morphological analyses. We asked whether place predictor of the impact of a parasitoid species on local host barcoding and morphology discover the same provisional species and dynamics is whether the parasitoid is a generalist or specialist. A whether the biological entities revealed by our analysis are congruent generalist, especially a mobile one, is viewed as stabilizing food webs with wasp host specificity. Morphological analysis revealed 171 (see ref. -
Hymenoptera: Braconidae: Microgastrinae) Comb
Revista Brasileira de Entomologia 63 (2019) 238–244 REVISTA BRASILEIRA DE Entomologia A Journal on Insect Diversity and Evolution www.rbentomologia.com Systematics, Morphology and Biogeography First record of Cotesia scotti (Valerio and Whitfield, 2009) (Hymenoptera: Braconidae: Microgastrinae) comb. nov. parasitising Spodoptera cosmioides (Walk, 1858) and Spodoptera eridania (Stoll, 1782) (Lepidoptera: Noctuidae) in Brazil a b a a Josiane Garcia de Freitas , Tamara Akemi Takahashi , Lara L. Figueiredo , Paulo M. Fernandes , c d e Luiza Figueiredo Camargo , Isabela Midori Watanabe , Luís Amilton Foerster , f g,∗ José Fernandez-Triana , Eduardo Mitio Shimbori a Universidade Federal de Goiás, Escola de Agronomia, Setor de Entomologia, Programa de Pós-Graduac¸ ão em Agronomia, Goiânia, GO, Brazil b Universidade Federal do Paraná, Setor de Ciências Agrárias, Programa de Pós-Graduac¸ ão em Agronomia – Produc¸ ão Vegetal, Curitiba, PR, Brazil c Universidade Federal de São Carlos, Programa de Pós-Graduac¸ ão em Ecologia e Recursos Naturais, São Carlos, SP, Brazil d Universidade Federal de São Carlos, Departamento de Ecologia e Biologia Evolutiva, São Carlos, SP, Brazil e Universidade Federal do Paraná, Departamento de Zoologia, Curitiba, PR, Brazil f Canadian National Collection of Insects, Ottawa, Canada g Universidade de São Paulo, Escola Superior de Agricultura “Luiz de Queiroz”, Departamento de Entomologia e Acarologia, Piracicaba, SP, Brazil a b s t r a c t a r t i c l e i n f o Article history: This is the first report of Cotesia scotti (Valerio and Whitfield) comb. nov. in Brazil, attacking larvae of the Received 3 December 2018 black armyworm, Spodoptera cosmioides, and the southern armyworm, S. -
The Evolution of Integrative Insect Systematics
Annual Research & Review in Biology 4(14): 2302-2317, 2014 SCIENCEDOMAIN international www.sciencedomain.org The Evolution of Integrative Insect Systematics S. N. Okiwelu1* and M. A. E. Noutcha1 1Entomology and Pest Management Unit, Department of Animal and Environmental Biology, University of Port Harcourt, Nigeria. Authors’ contributions This work was carried out in collaboration between both authors. Author MAEN managed the literature searches and provided useful information on nucleic acid sequencing. Author SNO wrote the protocol and produce the first draft of the manuscript. All authors read and approved the final manuscript. Received 4th November 2013 th Review Article Accepted 6 February 2014 Published 5th April 2014 ABSTRACT Background: Traditional morphological taxonomy fails in some cases; even when it succeeds, the use of other disciplines significantly accelerates identification and enhances our understanding of the processes in speciation. Arthropods: The arthropod tree of life is now divided into FIVE major branches: Pcynogonida, Euchelicerata, Myriapoda, Crustacea and Hexapoda. Crustacea and Hexapoda are in a clade, Tetraconata (Pancrustacea). Blattaria is more closely related to Isoptera; Strepsiptera is closely related to Coleoptera. History of Entomological Classification: This history is segregated into four periods: Pre-Linnaean era, First century spanning Linnaeus’ “Systema Naturae” to Darwin’s “On the Origin of species”, Darwinian Era up to the Cladistic Revolution, Hennigian Era leading to today. Classification in the pre-Linnaean era was based solely on morphological characteristics. Binomial nomenclature was developed in the first century. Phylogeny of insect orders along the lines of Darwinian evolution was evident in the third period. Hennigian Era utilized only taxa that are monophyletic. -
View the PDF File of the Tachinid Times, Issue 12
The Tachinid Times ISSUE 12 February 1999 Jim O’Hara, editor Agriculture & Agri-Food Canada, Biological Resources Program Eastern Cereal and Oilseed Research Centre C.E.F., Ottawa, Ontario, Canada, K1A 0C6 Correspondence: [email protected] The Tachinid Times began in 1988 when personal Evolution of Egg Structure in Tachinidae (by S.P. computers were gaining in popularity, yet before the Gaponov) advent of e-mail and the World Wide Web. A newsletter Using a scanning electron microscope I investigated distributed through the mail seemed like a useful the egg structure of 114 species of Tachinidae. The endeavour to foster greater awareness about the work of research was focused on the peculiarities of the egg others among researchers interested in the Tachinidae. surface and the structure of the aeropylar area. Data on Now, eleven years later, despite the speed and the method of egg-laying, the structure of the female convenience of e-mail and other advanced modes of reproductive system and the host range were also taken communication, this newsletter still seems to hold a place into consideration. Since any kind of adaptation is a in the distribution of news about the Tachinidae. If there result of evolution and every stage of ontogenesis, is sufficient interest - and submissions - over the course including the egg stage, is adapted to some specific of the next year, then another issue will appear in environmental conditions, each stage of ontogenesis February of the new millennium. As always, please send evolved more or less independently. The development of me your news for inclusion in the newsletter before the provisionary devices (coenogenetic adaptations) and their end of next January. -
Natural History of the Gila Symposium October 14–16, 2010 Western New Mexico University Silver City, New Mexico
the new mexico botanist Special Issue Number 3 October 2012 proceedings of the third Natural History of the Gila Symposium October 14–16, 2010 Western New Mexico University Silver City, New Mexico edited by William Norris Department of Natural Sciences, Western New Mexico University Richard Felger University of Arizona Herbarium and Department of Soil, Water and Environmental Science, University of Arizona 2012 Proceedings of the Third Natural History of the Gila Symposium, October 2010 / The New Mexico Botanist, Special Issue No. 3, October 2012 Contents Introduction .................................................................................................. 1 Some Things Going On in the Gila National Forest That You May Find Interesting Richard Markley .............................................................................................. 2 For Birds: Dale and Marian Zimmerman Gene Jercinovic ............................................................................................... 6 Visions of Dulcinea Mike Fugagli .................................................................................................15 Box Canyon Road Sharman Apt Russell ........................................................................................17 Exploring the Late Prehistoric Occupation of the Upper Gila Region Through Preservation Archaeology Katherine Dungan, Deborah Huntley, Jeffery Clark, Robert Jones, and Andrew Laurenzi ..............20 Review of Tachinid Fly Diversity in the Gila National Forest, New Mexico James E. -
1 Modern Threats to the Lepidoptera Fauna in The
MODERN THREATS TO THE LEPIDOPTERA FAUNA IN THE FLORIDA ECOSYSTEM By THOMSON PARIS A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2011 1 2011 Thomson Paris 2 To my mother and father who helped foster my love for butterflies 3 ACKNOWLEDGMENTS First, I thank my family who have provided advice, support, and encouragement throughout this project. I especially thank my sister and brother for helping to feed and label larvae throughout the summer. Second, I thank Hillary Burgess and Fairchild Tropical Gardens, Dr. Jonathan Crane and the University of Florida Tropical Research and Education center Homestead, FL, Elizabeth Golden and Bill Baggs Cape Florida State Park, Leroy Rogers and South Florida Water Management, Marshall and Keith at Mack’s Fish Camp, Susan Casey and Casey’s Corner Nursery, and Michael and EWM Realtors Inc. for giving me access to collect larvae on their land and for their advice and assistance. Third, I thank Ryan Fessendon and Lary Reeves for helping to locate sites to collect larvae and for assisting me to collect larvae. I thank Dr. Marc Minno, Dr. Roxanne Connely, Dr. Charles Covell, Dr. Jaret Daniels for sharing their knowledge, advice, and ideas concerning this project. Fourth, I thank my committee, which included Drs. Thomas Emmel and James Nation, who provided guidance and encouragement throughout my project. Finally, I am grateful to the Chair of my committee and my major advisor, Dr. Andrei Sourakov, for his invaluable counsel, and for serving as a model of excellence of what it means to be a scientist. -
Massively Parallel Multiplex DNA Sequencing for Specimen
OPEN Massively parallel multiplex DNA SUBJECT AREAS: sequencing for specimen identification GENETIC MARKERS BIODIVERSITY using an Illumina MiSeq platform Shadi Shokralla1, Teresita M. Porter2, Joel F. Gibson1, Rafal Dobosz1, Daniel H. Janzen3, Received Winnie Hallwachs3, G. Brian Golding2 & Mehrdad Hajibabaei1 7 January 2015 Accepted 1Department of Integrative Biology and Biodiversity Institute of Ontario, University of Guelph, 50 Stone Road East, Guelph, ON, 16 March 2015 Canada N1G 2W1, 2Department of Biology, McMaster University, 1280 Main Street West, Hamilton, ON, Canada L8S 4K1, 3Department of Biology, University of Pennsylvania, Philadelphia, PA, USA 19104. Published 17 April 2015 Genetic information is a valuable component of biosystematics, especially specimen identification through the use of species-specific DNA barcodes. Although many genomics applications have shifted to Correspondence and High-Throughput Sequencing (HTS) or Next-Generation Sequencing (NGS) technologies, sample identification (e.g., via DNA barcoding) is still most often done with Sanger sequencing. Here, we present a requests for materials scalable double dual-indexing approach using an Illumina Miseq platform to sequence DNA barcode should be addressed to markers. We achieved 97.3% success by using half of an Illumina Miseq flowcell to obtain 658 base pairs of S.S. (sshokral@ the cytochrome c oxidase I DNA barcode in 1,010 specimens from eleven orders of arthropods. Our uoguelph.ca) approach recovers a greater proportion of DNA barcode sequences from individuals than does conventional Sanger sequencing, while at the same time reducing both per specimen costs and labor time by nearly 80%. In addition, the use of HTS allows the recovery of multiple sequences per specimen, for deeper analysis of genetic variation in target gene regions. -
Insects on Palms
Insects on Palms i Insects on Palms F.W. Howard, D. Moore, R.M. Giblin-Davis and R.G. Abad CABI Publishing CABI Publishing is a division of CAB International CABI Publishing CABI Publishing CAB International 10 E 40th Street Wallingford Suite 3203 Oxon OX10 8DE New York, NY 10016 UK USA Tel: +44 (0)1491 832111 Tel: +1 (212) 481 7018 Fax: +44 (0)1491 833508 Fax: +1 (212) 686 7993 Email: [email protected] Email: [email protected] Web site: www.cabi.org © CAB International 2001. All rights reserved. No part of this publication may be repro- duced in any form or by any means, electronically, mechanically, by photocopying, recording or otherwise, without the prior permission of the copyright owners. A catalogue record for this book is available from the British Library, London, UK. Library of Congress Cataloging-in-Publication Data Insects on palms / by Forrest W. Howard … [et al.]. p. cm. Includes bibliographical references and index. ISBN 0-85199-326-5 (alk. paper) 1. Palms--Diseases and pests. 2. Insect pests. 3. Insect pests--Control. I. Howard, F. W. SB608.P22 I57 2001 634.9’74--dc21 00-057965 ISBN 0 85199 326 5 Typeset by Columns Design Ltd, Reading Printed and bound in the UK by Biddles Ltd, Guildford and King’s Lynn Contents List of Boxes vii Authors and Contributors viii Acknowledgements x Preface xiii 1 The Animal Class Insecta and the Plant Family Palmae 1 Forrest W. Howard 2 Defoliators of Palms 33 Lepidoptera 34 Forrest W. Howard and Reynaldo G. Abad Coleoptera 81 Forrest W.