Survey of the Terrestrial Arthropods Found in the Caves of Ghana
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Turkish Journal of Biodiversity
Turkish Journal of Biodiversity Turk J Biod, March 2020, 3(1): 21-31 https://doi.org/10.38059/biodiversity.698157 Journal homepage: http://turkbiod.artvin.edu.tr/ http://dergipark.gov.tr/biodiversity e-ISSN:2667-4386 RESEARCH ARTICLE Open Access Diversity of ants species in different habitat mosaics of Acharya Jagadish Chandra Bose Indian Botanical Garden (Howrah, West Bengal, India) Acharya Jagadish Chandra Bose Hindistan Botanik Bahçesi'nin (Howrah, Batı Bengal, Hindistan) farklı yaşam alanı mozaiklerinde karınca türlerinin çeşitliliği Arka GOSWAMI a* , Arijit CHATTERJEE a , Sheela SAROJ b a Department of Environmental Science, Asutosh College, Kolkata, India b Zoological Survey of India, Ministry of Environment, Forest and Climate Change, Kolkata, India Article Info ABSTRACT ©2020 Ali Nihat Gökyiğit Botanical Ants (Hymenoptera, Formicidae) occupy a wide range of ecological niches and exploit various food Garden Application and Research resources either as herbivores or as predators or scavengers. This study establishes the diversity of Center of Artvin Coruh University. ants in an ex-situ conservation site dedicated for plants known as Indian Botanical garden situated amidst a congested city. It also documents the relation of ant community structure with different *Corresponding author: habitat mosaics present within this protected area. For this study pit fall trap was used as collection e-mail:[email protected] method and amalgamated within quadrat sampling (total 16 quadrats and each quadrat contains 9 ORCID: 0000-0002-8932-5113 pit fall traps placed uniformly) distributed in four different habitats and repeated in two consecutive Article history months. All the specimens were collected, preserved and identified meticulously. Total 27 species of Received: March 3, 2012 ants from 19 genera and 6 subfamilies are documented from the whole study area. -
Fossil Insects.*
ANNALS OF The Entomological Society of America Downloaded from https://academic.oup.com/aesa/article/10/1/1/8284 by guest on 25 September 2021 Volume X MARCH, 19 17 Number 1 FOSSIL INSECTS.* By T. D. A. COCKERELL. In these serious days, it seems just a little grotesque that I should cross half a continent to address you on a subject so remote from the current of human life as fossil insects. The limitations of our society do indeed forbid such topics as the causes of the war or the evil effects of intercollegiate athletics; but I might have chosen to discuss lice or mosquitoes—any of those insects whose activities have before now decided the fate of nations. My excuse for avoiding these more lively topics only aggravates the offense, for it is the fact that I have never given them adequate attention, but have in the past ten years occupied myself with matters having for the most part no obvious economic application. There is, however, another point of view. Many years ago I had the good fortune to meet the eminent ornithologist, Elliott Coues, at Santa Fe. We spent a considerable part of the night discussing a variety of subjects, from spiritualism to rattlesnakes, and when we parted he made a remark which those who knew him will recognize as characteristic. He said, "Cockerell, I really believe that if it had not been for science, you would have been a dangerous crank!" Surely experience and history alike confirm the essential sagacity of the observa tion, as applied not merely to your lecturer, but to mankind in general. -
Insecta: Hymenoptera: Formicidae): Type Specimens Deposited in the Natural History Museum Vienna (Austria) and a Preliminary Checklist
Ann. Naturhist. Mus. Wien, B 121 9–18 Wien, Februar 2019 Notes on the ant fauna of Eritrea (Insecta: Hymenoptera: Formicidae): type specimens deposited in the Natural History Museum Vienna (Austria) and a preliminary checklist M. Madl* Abstract The ant collection of the Natural History Museum Vienna (Austria) contains syntypes of nine species described from Eritrea: Aphaenogaster clavata EMERY, 1877 (= Pheidole clavata (EMERY, 1877)), Cam- ponotus carbo EMERY, 1877, Melissotarsus beccarii EMERY, 1877, Monomorium bicolor EMERY, 1877, Pheidole rugaticeps EMERY, 1877, Pheidole speculifera EMERY, 1877, Polyrhachis antinorii EMERY, 1877 (= Polyrhachis viscosa SMITH, 1858) and Tetramorium doriae EMERY, 1881. All syntypes were collected in Eritrea except the syntype of Monomorium luteum EMERY, 1881, which was collected in Yemen. A prelimi- nary checklist of the ants of Eritrea comprises 114 species and subspecies of seven subfamilies. Zusammenfassung In der Ameisensammlung des Naturhistorischen Museums Wien (Österreich) werden Syntypen von neun Arten aufbewahrt, die aus Eritrea beschrieben worden sind: Aphaenogaster clavata EMERY, 1877 [= Phei- dole clavata (EMERY, 1877)], Camponotus carbo EMERY, 1877, Melissotarsus beccarii EMERY, 1877, Mono- morium bicolor EMERY, 1877, Pheidole rugaticeps EMERY, 1877, Pheidole speculifera EMERY, 1877, Poly- rhachis antinorii EMERY, 1877 (= Polyrhachis viscosa SMITH, 1858) und Tetramorium doriae EMERY, 1881. Alle Syntypen stammen aus Eritrea ausgenommen der Syntypus von Monomorium luteum EMERY, 1881, der in Jemen gesammelt wurde. Eine vorläufige Artenliste der Ameisen Eritreas umfasst 114 Arten und Unterarten aus sieben Unterfamilien. Key words: Formicidae, types, Camponotus, Melissotarsus, Monomorium, Pheidole, Polyrhachis, Tetra- morium, checklist, Eritrea, Yemen. Introduction The study of the ant fauna of Eritrea has been neglected for several decades. -
Movement of Plastic-Baled Garbage and Regulated (Domestic) Garbage from Hawaii to Landfills in Oregon, Idaho, and Washington
Movement of Plastic-baled Garbage and Regulated (Domestic) Garbage from Hawaii to Landfills in Oregon, Idaho, and Washington. Final Biological Assessment, February 2008 Table of Contents I. Introduction and Background on Proposed Action 3 II. Listed Species and Program Assessments 28 Appendix A. Compliance Agreements 85 Appendix B. Marine Mammal Protection Act 150 Appendix C. Risk of Introduction of Pests to the Continental United States via Municipal Solid Waste from Hawaii. 159 Appendix D. Risk of Introduction of Pests to Washington State via Municipal Solid Waste from Hawaii 205 Appendix E. Risk of Introduction of Pests to Oregon via Municipal Solid Waste from Hawaii. 214 Appendix F. Risk of Introduction of Pests to Idaho via Municipal Solid Waste from Hawaii. 233 2 I. Introduction and Background on Proposed Action This biological assessment (BA) has been prepared by the United States Department of Agriculture (USDA), Animal and Plant Health Inspection Service (APHIS) to evaluate the potential effects on federally-listed threatened and endangered species and designated critical habitat from the movement of baled garbage and regulated (domestic) garbage (GRG) from the State of Hawaii for disposal at landfills in Oregon, Idaho, and Washington. Specifically, garbage is defined as urban (commercial and residential) solid waste from municipalities in Hawaii, excluding incinerator ash and collections of agricultural waste and yard waste. Regulated (domestic) garbage refers to articles generated in Hawaii that are restricted from movement to the continental United States under various quarantine regulations established to prevent the spread of plant pests (including insects, disease, and weeds) into areas where the pests are not prevalent. -
Taxonomic Classification of Ants (Formicidae)
bioRxiv preprint doi: https://doi.org/10.1101/407452; this version posted September 4, 2018. 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 4.0 International license. Taxonomic Classification of Ants (Formicidae) from Images using Deep Learning Marijn J. A. Boer1 and Rutger A. Vos1;∗ 1 Endless Forms, Naturalis Biodiversity Center, Leiden, 2333 BA, Netherlands *[email protected] Abstract 1 The well-documented, species-rich, and diverse group of ants (Formicidae) are important 2 ecological bioindicators for species richness, ecosystem health, and biodiversity, but ant 3 species identification is complex and requires specific knowledge. In the past few years, 4 insect identification from images has seen increasing interest and success, with processing 5 speed improving and costs lowering. Here we propose deep learning (in the form of a 6 convolutional neural network (CNN)) to classify ants at species level using AntWeb 7 images. We used an Inception-ResNet-V2-based CNN to classify ant images, and three 8 shot types with 10,204 images for 97 species, in addition to a multi-view approach, for 9 training and testing the CNN while also testing a worker-only set and an AntWeb 10 protocol-deviant test set. Top 1 accuracy reached 62% - 81%, top 3 accuracy 80% - 92%, 11 and genus accuracy 79% - 95% on species classification for different shot type approaches. 12 The head shot type outperformed other shot type approaches. -
New Cockroaches (Dictyoptera: Blattina) from Baltic Amber, with Description of a New Genus and Species: Stegoblatta Irmgardgroeh
Proceedings of the Zoological Institute RAS Vol. 316, No. 3, 2012, рр. 193–202 УДК 595.722 NEW COCKROACHES (DICTYOPTERA: BLATTINA) FROM BALTIC AMBER, WITH THE DESCRIPTION OF A NEW GENUS AND SPECIES: STEGOBLATTA IRMGARDGROEHNI L.N. Anisyutkin1* and C. Gröhn2 1Zoological Institute of the Russian Academy of Sciences, Universitetskaya Emb. 1, 199034 Saint Petersburg, Russia; e-mail: [email protected] 2Bünebüttler Weg 7, D-21509 Glinde/Hamburg, Germany; e-mail: [email protected] ABSTRACT A new genus and species of cockroaches, Stegoblatta irmgardgroehni gen. et sp. nov. is described from Baltic Amber. The taxonomic position of the new genus is discussed and it is concluded that it belongs to the family Blaberidae. The male of Paraeuthyrrapha groehni (Corydiidae, Euthyrrhaphinae) is described for the first time. Key words: Baltic Amber, Blaberidae, cockroaches, Dictyoptera, Paraeuthyrrapha groehni, Stegoblatta irmgard- groehni gen. et sp. nov. НОВЫЕ ТАРАКАНЫ (DICTYOPTERA: BLATTINA) ИЗ БАЛТИЙСКОГО ЯНТАРЯ, С ОПИСАНИЕМ НОВОГО РОДА И ВИДА: STEGOBLATTA IRMGARDGROEHNI Л.Н. Анисюткин1* и К. Грён2 1Зоологический институт Российской академии наук, Университетская наб. 1, 199034 Санкт-Петербург, Россия; e-mail: [email protected] 2Bünebüttler Weg 7, D-21509 Glinde/Hamburg, Germany; e-mail: [email protected] РЕЗЮМЕ Новый род и вид тараканов (Stegoblatta irmgardgroehni gen. et sp. nov.) описывается из балтийского янта- ря. Обсуждается таксономическое положение нового рода, предположительно отнесенного к семейству Blaberidae. Впервые описывается самец Paraeuthyrrhapha groehni (Corydiidae, Euthyrrhaphinae). Ключевые слова: балтийский янтарь, Blaberidae, тараканы, Dictyoptera, Paraeuthyrrapha groehni, Stegoblatta irmgardgroehni gen. et sp. nov. INTRODUCTION Wichard 2010). The cockroach fauna from Baltic amber is more or less similar to the modern one in Baltic amber is one of the most famous sources of taxa composition (Shelford 1910, 1911; Weitshat fossil insects. -
RESEARCH ARTICLE Revision of the African Ants of The
TAES 143: 7-71 RESEARCH ARTICLE ISSO 0002-8320 http://taes.entomology-aes.org/ Revision of the African ants of the Bothroponera sulcata species complex (Hymenoptera: Formicidae: Ponerinae) ABDULMENEEM M. A. JOMA1,2 AND WILLIAM P. MACKAY2 1Department of Zoology, Faculty of Sciences, The University of Sebha, P.O. Box 18758, Sebha, Libya, alnoure69@ hotmail.com 2Department of Biological Sciences, Ecology and Evolutionary Biology Program, The University of Texas at El Paso, 500 West University Avenue, El Paso, TX 79968, USA, [email protected] ABSTRACT The Bothroponera sulcata ant species complex is distributed in Afrotropical areas, including tropical and subtropical ecosystems and is part of a poorly known group of ants. The sulcata species complex now includes 10 species, including 3 new species, 2 taxa elevated to species status and 7 new synonyms: B. ancilla Emery, B. crassa Emery, B. crassior Santschi (= B. ilgii syn. nov., Pachycondyla (Bothroponera) crassa st. crassior var. andrieui referred here), B. kruegeri Forel (= B. asina syn. nov., = B. rhodesiana syn. nov.), B. notaula (sp. nov.), B. picardi Forel, B. pilosuperficia(sp. nov.), B. ryderae (sp. nov.), B. silvestrii Santschi (= B. kenyensis syn. nov., = B. nimba syn. nov.) and B. soror Emery (= B. lamottei syn. nov., = B. suturalis (syn. nov.). The main defining character of this complex is the presence of a metatibial gland; however, there are other characters such as the shape of the anterior clypeal border, mandible surface and shape, teeth number and posterior dorsopropodeal shape (broadly or strongly curved or angulated). Diagnosis, comparisons, illustrations, distributions and other information about the species are provided with a key for the worker caste. -
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. -
Hymenoptera: Formicidae: Ponerinae)
Molecular Phylogenetics and Taxonomic Revision of Ponerine Ants (Hymenoptera: Formicidae: Ponerinae) Item Type text; Electronic Dissertation Authors Schmidt, Chris Alan Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 10/10/2021 23:29:52 Link to Item http://hdl.handle.net/10150/194663 1 MOLECULAR PHYLOGENETICS AND TAXONOMIC REVISION OF PONERINE ANTS (HYMENOPTERA: FORMICIDAE: PONERINAE) by Chris A. Schmidt _____________________ A Dissertation Submitted to the Faculty of the GRADUATE INTERDISCIPLINARY PROGRAM IN INSECT SCIENCE In Partial Fulfillment of the Requirements For the Degree of DOCTOR OF PHILOSOPHY In the Graduate College THE UNIVERSITY OF ARIZONA 2009 2 2 THE UNIVERSITY OF ARIZONA GRADUATE COLLEGE As members of the Dissertation Committee, we certify that we have read the dissertation prepared by Chris A. Schmidt entitled Molecular Phylogenetics and Taxonomic Revision of Ponerine Ants (Hymenoptera: Formicidae: Ponerinae) and recommend that it be accepted as fulfilling the dissertation requirement for the Degree of Doctor of Philosophy _______________________________________________________________________ Date: 4/3/09 David Maddison _______________________________________________________________________ Date: 4/3/09 Judie Bronstein -
Taxa Names List 6-30-21
Insects and Related Organisms Sorted by Taxa Updated 6/30/21 Order Family Scientific Name Common Name A ACARI Acaridae Acarus siro Linnaeus grain mite ACARI Acaridae Aleuroglyphus ovatus (Troupeau) brownlegged grain mite ACARI Acaridae Rhizoglyphus echinopus (Fumouze & Robin) bulb mite ACARI Acaridae Suidasia nesbitti Hughes scaly grain mite ACARI Acaridae Tyrolichus casei Oudemans cheese mite ACARI Acaridae Tyrophagus putrescentiae (Schrank) mold mite ACARI Analgidae Megninia cubitalis (Mégnin) Feather mite ACARI Argasidae Argas persicus (Oken) Fowl tick ACARI Argasidae Ornithodoros turicata (Dugès) relapsing Fever tick ACARI Argasidae Otobius megnini (Dugès) ear tick ACARI Carpoglyphidae Carpoglyphus lactis (Linnaeus) driedfruit mite ACARI Demodicidae Demodex bovis Stiles cattle Follicle mite ACARI Demodicidae Demodex brevis Bulanova lesser Follicle mite ACARI Demodicidae Demodex canis Leydig dog Follicle mite ACARI Demodicidae Demodex caprae Railliet goat Follicle mite ACARI Demodicidae Demodex cati Mégnin cat Follicle mite ACARI Demodicidae Demodex equi Railliet horse Follicle mite ACARI Demodicidae Demodex folliculorum (Simon) Follicle mite ACARI Demodicidae Demodex ovis Railliet sheep Follicle mite ACARI Demodicidae Demodex phylloides Csokor hog Follicle mite ACARI Dermanyssidae Dermanyssus gallinae (De Geer) chicken mite ACARI Eriophyidae Abacarus hystrix (Nalepa) grain rust mite ACARI Eriophyidae Acalitus essigi (Hassan) redberry mite ACARI Eriophyidae Acalitus gossypii (Banks) cotton blister mite ACARI Eriophyidae Acalitus vaccinii -
The Higher Classification of the Ant Subfamily Ponerinae (Hymenoptera: Formicidae), with a Review of Ponerine Ecology and Behavior
Zootaxa 3817 (1): 001–242 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3817.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:A3C10B34-7698-4C4D-94E5-DCF70B475603 ZOOTAXA 3817 The Higher Classification of the Ant Subfamily Ponerinae (Hymenoptera: Formicidae), with a Review of Ponerine Ecology and Behavior C.A. SCHMIDT1 & S.O. SHATTUCK2 1Graduate Interdisciplinary Program in Entomology and Insect Science, Gould-Simpson 1005, University of Arizona, Tucson, AZ 85721-0077. Current address: Native Seeds/SEARCH, 3584 E. River Rd., Tucson, AZ 85718. E-mail: [email protected] 2CSIRO Ecosystem Sciences, GPO Box 1700, Canberra, ACT 2601, Australia. Current address: Research School of Biology, Australian National University, Canberra, ACT, 0200 Magnolia Press Auckland, New Zealand Accepted by J. Longino: 21 Mar. 2014; published: 18 Jun. 2014 C.A. SCHMIDT & S.O. SHATTUCK The Higher Classification of the Ant Subfamily Ponerinae (Hymenoptera: Formicidae), with a Review of Ponerine Ecology and Behavior (Zootaxa 3817) 242 pp.; 30 cm. 18 Jun. 2014 ISBN 978-1-77557-419-4 (paperback) ISBN 978-1-77557-420-0 (Online edition) FIRST PUBLISHED IN 2014 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2014 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. -
The Evolutionary Significance of Rotation of the Oötheca in The
A PSYCHE Vol. 74 June, 1967 No. 2 THE EVOLUTIONARY SIGNIFICANCE OF ROTATION OF THE OOTHECA IN THE BLATTAR I By Louis M. Roth Pioneering Research Division U.S. Army Natick Laboratories, Natick Mass. ? The newly-formed ootheca of all cockroaches projects from the female in a vertical position, with the keel and micropylar ends of the eggs dorsally oriented. All of the Blattoidea (Fig. 1) and some of the Blaberoidea carry the egg case without changing this position. However, in some of the Polyphagidae (Figs. 11-16) and Blattellidae (Figs. 2,3), and all of the Blaberidae, the female rotates the ootheca 90° so that the keel faces laterally at the time it is deposited on a substrate (Polyphagidae, Blattellidae), carried for the entire embryo- genetic period ( Blattella spp.), or retracted into the uterus (all Blaberidae). According to McKittrick (1964), rotation of the ootheca frees the keel from the valve bases which block an anterior movement of the ootheca while it is in a vertical position, and it orients the ootheca so that its height lies in the plane of the cock- roach’s width, thus making it possible to move the egg case anteriorly beyond the valve. It is likely that by the time the ootheca had evolved to the stage where it was retracted internally, the height of the keel had been greatly reduced (e.g., in Blattella spp.) and it would not be necessary to free its keel from the valve bases. The eggs of Blaberidae increase greatly in size in the uterus during embryogenesis (Roth and Willis, 1955a, 1955b).