Coleoptera: Coccinellidae) of Iowa, U.S.A
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The 2014 Golden Gate National Parks Bioblitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 ON THIS PAGE Photograph of BioBlitz participants conducting data entry into iNaturalist. Photograph courtesy of the National Park Service. ON THE COVER Photograph of BioBlitz participants collecting aquatic species data in the Presidio of San Francisco. Photograph courtesy of National Park Service. The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 Elizabeth Edson1, Michelle O’Herron1, Alison Forrestel2, Daniel George3 1Golden Gate Parks Conservancy Building 201 Fort Mason San Francisco, CA 94129 2National Park Service. Golden Gate National Recreation Area Fort Cronkhite, Bldg. 1061 Sausalito, CA 94965 3National Park Service. San Francisco Bay Area Network Inventory & Monitoring Program Manager Fort Cronkhite, Bldg. 1063 Sausalito, CA 94965 March 2016 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado, publishes a range of reports that address natural resource topics. These reports are of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Report Series is used to disseminate comprehensive information and analysis about natural resources and related topics concerning lands managed by the National Park Service. -
Ladybirds, Ladybird Beetles, Lady Beetles, Ladybugs of Florida, Coleoptera: Coccinellidae1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY-170 Ladybirds, Ladybird beetles, Lady Beetles, Ladybugs of Florida, Coleoptera: Coccinellidae1 J. H. Frank R. F. Mizell, III2 Introduction Ladybird is a name that has been used in England for more than 600 years for the European beetle Coccinella septempunctata. As knowledge about insects increased, the name became extended to all its relatives, members of the beetle family Coccinellidae. Of course these insects are not birds, but butterflies are not flies, nor are dragonflies, stoneflies, mayflies, and fireflies, which all are true common names in folklore, not invented names. The lady for whom they were named was "the Virgin Mary," and common names in other European languages have the same association (the German name Marienkafer translates Figure 1. Adult Coccinella septempunctata Linnaeus, the to "Marybeetle" or ladybeetle). Prose and poetry sevenspotted lady beetle. Credits: James Castner, University of Florida mention ladybird, perhaps the most familiar in English being the children's rhyme: Now, the word ladybird applies to a whole Ladybird, ladybird, fly away home, family of beetles, Coccinellidae or ladybirds, not just Your house is on fire, your children all gone... Coccinella septempunctata. We can but hope that newspaper writers will desist from generalizing them In the USA, the name ladybird was popularly all as "the ladybird" and thus deluding the public into americanized to ladybug, although these insects are believing that there is only one species. There are beetles (Coleoptera), not bugs (Hemiptera). many species of ladybirds, just as there are of birds, and the word "variety" (frequently use by newspaper 1. -
Cambridge University Press 978-1-107-11607-8 — a Natural History of Ladybird Beetles M. E. N. Majerus , Executive Editor H. E. Roy , P
Cambridge University Press 978-1-107-11607-8 — A Natural History of Ladybird Beetles M. E. N. Majerus , Executive Editor H. E. Roy , P. M. J. Brown Index More Information Index 2-isopropyl-3-methoxy-pyrazine, 238 281, 283, 285, 287–9, 291–5, 297–8, 2-phenylethylamine, 237 301–3, 311, 314, 316, 319, 325, 327, 329, 335 abdomen, 17, 20, 22, 24, 28–9, 32, 38, 42, 110, Adalia 4-spilota,80 114, 125, 128, 172, 186, 189, 209–10, Adalia conglomerata, 255 218 adaline, 108, 237, 241 Acacia, 197, 199 adalinine, 237 acaricides, 316 adelgids, 29, 49, 62, 65, 86, 91, 176, 199, 308, Acaridae, 217 310, 322 Acarina, 205, 217 Adonia, 44, 71 Acer pseudoplatanus, 50, 68, 121 aggregations, 163, 165, 168, 170, 178, 184, Acraea, 228, 297, 302 221, 312, 324 Acraea encedana, 302 Aiolocaria, 78, 93, 133, 276 Acraea encedon, 297, 302 Aiolocaria hexaspilota,78 Acyrthosiphon nipponicum, 101 Aiolocaria mirabilis, 133, 276 Acyrthosiphon pisum, 75, 77, 90, 92, 97–101, albino, 273 116, 239 Alces alces,94 Adalia, 5–6, 10, 22, 34, 44, 64, 70, 78, 80, 86, Aleyrodidae, 91, 310 123, 125, 128, 130, 132, 140, 143, 147, alfalfa, 119, 308, 316, 319, 325 159–60, 166–7, 171, 180–1, 218, 222, alimentary canal, 29, 35, 221 234, 237, 239, 241, 255, 259–60, 262, alkaloids, x, 99–100, 195–7, 202, 236–9, 241–2, 269, 279, 281, 284, 286, 298, 311, 325, 245–6 327, 335 Allantonematidae, 220 Adalia 10-punctata, 22, 70, 80, 86, 98–100, anal cremaster, 38, 40 104, 108, 116, 132, 146–7, 149, Anatis, 4, 17, 23, 41, 44, 66, 76, 89, 102, 131, 154, 156, 160, 174, 181–3, 188, 148, 165, 186, 191, 193, -
Lessons from Genome Skimming of Arthropod-Preserving Ethanol Benjamin Linard, P
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Archive Ouverte en Sciences de l'Information et de la Communication Lessons from genome skimming of arthropod-preserving ethanol Benjamin Linard, P. Arribas, C. Andújar, A. Crampton-Platt, A. P. Vogler To cite this version: Benjamin Linard, P. Arribas, C. Andújar, A. Crampton-Platt, A. P. Vogler. Lessons from genome skimming of arthropod-preserving ethanol. Molecular Ecology Resources, Wiley/Blackwell, 2016, 16 (6), pp.1365-1377. 10.1111/1755-0998.12539. hal-01636888 HAL Id: hal-01636888 https://hal.archives-ouvertes.fr/hal-01636888 Submitted on 17 Jan 2019 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. 1 Lessons from genome skimming of arthropod-preserving 2 ethanol 3 Linard B.*1,4, Arribas P.*1,2,5, Andújar C.1,2, Crampton-Platt A.1,3, Vogler A.P. 1,2 4 5 1 Department of Life Sciences, Natural History Museum, Cromwell Road, London SW7 6 5BD, UK, 7 2 Department of Life Sciences, Imperial College London, Silwood Park Campus, Ascot 8 SL5 7PY, UK, 9 3 Department -
Arthropod IGF, Relaxin and Gonadulin, Putative Orthologs of Drosophila
bioRxiv preprint doi: https://doi.org/10.1101/2020.05.11.088476; this version posted June 10, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Arthropod IGF, Relaxin and Gonadulin, putative 2 orthologs of Drosophila insulin-like peptides 6, 7 and 3 8, likely originated from an ancient gene triplication 4 5 6 Jan A. Veenstra1, 7 8 1 INCIA UMR 5287 CNRS, University of Bordeaux, Bordeaux, Pessac, France 9 10 Corresponding Author: 11 Jan A. Veenstra1 12 INCIA UMR 5287 CNRS, Université de Bordeaux, allée Geoffroy St Hillaire, CS 50023, 33 615 13 Pessac Cedex, France 14 Email address: [email protected] 15 16 Abstract 17 Background. Insects have several genes coding for insulin-like peptides and they have been 18 particularly well studied in Drosophila. Some of these hormones function as growth hormones 19 and are produced by the fat body and the brain. These act through a typical insulin receptor 20 tyrosine kinase. Two other Drosophila insulin-like hormones are either known or suspected to act 21 through a G-protein coupled receptor. Although insulin-related peptides are known from other 22 insect species, Drosophila insulin-like peptide 8, one that uses a G-protein coupled receptor, has 23 so far only been identified from Drosophila and other flies. However, its receptor is widespread 24 within arthropods and hence it should have orthologs. Such putative orthologs were recently 25 identified in decapods and have been called gonadulins. -
Modification of Insect and Arachnid Behaviours by Vertically Transmitted Endosymbionts: Infections As Drivers of Behavioural Change and Evolutionary Novelty
Insects 2012, 3, 246-261; doi:10.3390/insects3010246 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Review Modification of Insect and Arachnid Behaviours by Vertically Transmitted Endosymbionts: Infections as Drivers of Behavioural Change and Evolutionary Novelty Sara L. Goodacre 1,* and Oliver Y. Martin 2 1 School of Biology, University of Nottingham, NG7 2RD, UK 2 ETH Zurich, Experimental Ecology, Institute for Integrative Biology, Universitätsstrasse 16, CH-8092 Zurich, Switzerland; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +44-115-8230334. Received: 29 January 2012; in revised form: 17 February 2012 / Accepted: 21 February 2012 / Published: 29 February 2012 Abstract: Vertically acquired, endosymbiotic bacteria such as those belonging to the Rickettsiales and the Mollicutes are known to influence the biology of their arthropod hosts in order to favour their own transmission. In this study we investigate the influence of such reproductive parasites on the behavior of their insects and arachnid hosts. We find that changes in host behavior that are associated with endosymbiont infections are not restricted to characteristics that are directly associated with reproduction. Other behavioural traits, such as those involved in intraspecific competition or in dispersal may also be affected. Such behavioural shifts are expected to influence the level of intraspecific variation and the rate at which adaptation can occur through their effects on effective population size and gene flow amongst populations. Symbionts may thus influence both levels of polymorphism within species and the rate at which diversification can occur. -
Historical, Landscape and Resource Influences on the Coccinellid Community in Missouri
HISTORICAL, LANDSCAPE AND RESOURCE INFLUENCES ON THE COCCINELLID COMMUNITY IN MISSOURI _______________________________________ A Dissertation presented to the Faculty of the Graduate School at the University of Missouri-Columbia _______________________________________________________ In Partial Fulfillment of the requirements for the Degree Doctor of Philosophy _____________________________________________________ by LAUREN M. DIEPENBROCK Dr. Deborah Finke, Dissertation Supervisor MAY 2014 The undersigned, appointed by the Dean of the Graduate School, have examined the dissertation entitled: HISTORICAL, LANDSCAPE AND RESOURCE INFLUENCES ON THE COCCINELLID COMMUNITY IN MISSOURI Presented by Lauren M. Diepenbrock a candidate for the degree of Doctor of Philosophy and hereby certify that in their opinion is worthy of acceptance ________________________________________________ Dr. Deborah Finke, Dissertation Supervisor, Division of Plant Sciences ________________________________________________ Dr. Richard Houseman, Division of Plant Sciences ________________________________________________ Dr. Bruce Barrett, Division of Plant Sciences ________________________________________________ Dr. John Faaborg, Division of Biological Sciences ACKNOWLEDGEMENTS I would like to thank my Ph. D. advisor, Dr. Deborah Finke for the opportunity to pursue a doctoral degree in insect ecology and for her guidance and support throughout my time at the University of Missouri. I would also like to thank my graduate committee, Drs. Houseman, Barrett and Faaborg for their helpful advice during this academic journey. In addition to my graduate committee, I am grateful for the advice and opportunities that were made available to me by Dr. Rose-Marie Muzika, who introduced me to the Conservation Biology certificate program and all of the great researchers across the university who share my interests in biodiversity conservation. I will always be grateful to Dr. Jeanne Mihail for introducing me to Dr. -
Survey of Predatory Coccinellids (Coleoptera
Survey of Predatory Coccinellids (Coleoptera: Coccinellidae) in the Chitral District, Pakistan Author(s): Inamullah Khan, Sadrud Din, Said Khan Khalil and Muhammad Ather Rafi Source: Journal of Insect Science, 7(7):1-6. 2007. Published By: Entomological Society of America DOI: http://dx.doi.org/10.1673/031.007.0701 URL: http://www.bioone.org/doi/full/10.1673/031.007.0701 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. Journal of Insect Science | www.insectscience.org ISSN: 1536-2442 Survey of predatory Coccinellids (Coleoptera: Coccinellidae) in the Chitral District, Pakistan Inamullah Khan, Sadrud Din, Said Khan Khalil and Muhammad Ather Rafi1 Department of Plant Protection, NWFP Agricultural University, Peshawar, Pakistan 1 National Agricultural Research Council, Islamabad, Pakistan Abstract An extensive survey of predatory Coccinellid beetles (Coleoptera: Coccinellidae) was conducted in the Chitral District, Pakistan, over a period of 7 months (April through October, 2001). -
Bionomics of Chilocorus Infernalis Mulsant, 1853 (Coleoptera
doi:10.14720/aas.2019.113.1.07 Original research article / izvirni znanstveni članek Bionomics of Chilocorus infernalis Mulsant, 1853 (Coleoptera: Coccinellidae), a predator of San Jose scale, Diaspidiotus perniciosus (Comstock, 1881) under laboratory conditions Razia RASHEED1*, A.A. BUHROO1 and Shaziya GULL1 Received July 23, 2018; accepted January 03, 2019. Delo je prispelo 23. julija 2018, sprejeto 03. januarja 2019. ABSTRACT IZVLEČEK The bionomics of Chilocorus infernalis Mulsant, 1853, a BIONOMIJA VRSTE Chilocorus infernalis Mulsant, 1853 natural enemy of San Jose scale, was studied under laboratory (Coleoptera: Coccinellidae), PLENILCA AMERIŠKEGA conditions (26 ± 2˚C, and 65 ± 5% relative humidity). The KAPARJA (Diaspidiotus perniciosus (Comstock, 1881)) V eggs were deposited in groups and on average 45.68 ± 24.70 LABORATORIJSKIH RAZMERAH eggs were laid by female. Mean observed incubation period was 6.33 ± 1.52 days. Four instar grubs were observed, and Bionomija vrste Chilocorus infernalis Mulsant, 1853, mean duration of all four grubs was found to be 19.98 days. naravnega sovražnika ameriškega kaparja, je bila preučevana The pupal stage lasted for 8.00 ± 0.50 days and after adults v laboratorijskih razmerah (26 ± 2˚C in 65 ± 5 % relativne emerged out. zračne vlažnosti). Samice plenilca so jajčeca odlagale v skupinah, v poprečju 45,68 ± 24,70 jajčec na samico. V Key words: bionomics; natural enemies; San Jose scale; povprečju so se ličinke razvile iz jajčec v 6,33 ± 1,52 dneh. incubation period; larval instars Ugotovljene so bile štiri larvalne stopnje, katerih povprečna življenska doba je bila 19,98 dni. Razvojni štadij bube je trajal 8,00 ± 0,50 dni, nakar so se izlegli imagi. -
COLEOPTERA COCCINELLIDAE) INTRODUCTIONS and ESTABLISHMENTS in HAWAII: 1885 to 2015
AN ANNOTATED CHECKLIST OF THE COCCINELLID (COLEOPTERA COCCINELLIDAE) INTRODUCTIONS AND ESTABLISHMENTS IN HAWAII: 1885 to 2015 JOHN R. LEEPER PO Box 13086 Las Cruces, NM USA, 88013 [email protected] [1] Abstract. Blackburn & Sharp (1885: 146 & 147) described the first coccinellids found in Hawaii. The first documented introduction and successful establishment was of Rodolia cardinalis from Australia in 1890 (Swezey, 1923b: 300). This paper documents 167 coccinellid species as having been introduced to the Hawaiian Islands with forty-six (46) species considered established based on unpublished Hawaii State Department of Agriculture records and literature published in Hawaii. The paper also provides nomenclatural and taxonomic changes that have occurred in the Hawaiian records through time. INTRODUCTION The Coccinellidae comprise a large family in the Coleoptera with about 490 genera and 4200 species (Sasaji, 1971). The majority of coccinellid species introduced into Hawaii are predacious on insects and/or mites. Exceptions to this are two mycophagous coccinellids, Calvia decimguttata (Linnaeus) and Psyllobora vigintimaculata (Say). Of these, only P. vigintimaculata (Say) appears to be established, see discussion associated with that species’ listing. The members of the phytophagous subfamily Epilachninae are pests themselves and, to date, are not known to be established in Hawaii. None of the Coccinellidae in Hawaii are thought to be either endemic or indigenous. All have been either accidentally or purposely introduced. Three species, Scymnus discendens (= Diomus debilis LeConte), Scymnus ocellatus (=Scymnobius galapagoensis (Waterhouse)) and Scymnus vividus (= Scymnus (Pullus) loewii Mulsant) were described by Sharp (Blackburn & Sharp, 1885: 146 & 147) from specimens collected in the islands. There are, however, no records of introduction for these species prior to Sharp’s descriptions. -
Co-Invasion of the Ladybird Harmonia Axyridis and Its Parasites Hesperomyces Virescens Fungus and Parasitylenchus Bifurcatus
bioRxiv preprint doi: https://doi.org/10.1101/390898; this version posted August 13, 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. 1 Co-invasion of the ladybird Harmonia axyridis and its parasites Hesperomyces virescens fungus and 2 Parasitylenchus bifurcatus nematode to the Caucasus 3 4 Marina J. Orlova-Bienkowskaja1*, Sergei E. Spiridonov2, Natalia N. Butorina2, Andrzej O. Bieńkowski2 5 6 1 Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia 7 2A.N. Severtsov Institute of Ecology and Evolution, Russian Academy of Sciences, Moscow, Russia 8 * Corresponding author (MOB) 9 E-mail: [email protected] 10 11 Short title: Co-invasion of Harmonia axyridis and its parasites to the Caucasus 12 13 Abstract 14 Study of parasites in recently established populations of invasive species can shed lite on sources of 15 invasion and possible indirect interactions of the alien species with native ones. We studied parasites of 16 the global invader Harmonia axyridis (Coleoptera: Coccinellidae) in the Caucasus. In 2012 the first 17 established population of H. axyridis was recorded in the Caucasus in Sochi (south of European Russia, 18 Black sea coast). By 2018 the ladybird has spread to the vast territory: Armenia, Georgia and south 19 Russia: Adygea, Krasnodar territory, Stavropol territory, Dagestan, Kabardino-Balkaria and North 20 Ossetia. Examination of 213 adults collected in Sochi in 2018 have shown that 53% of them are infested 21 with Hesperomyces virescens fungi (Ascomycota: Laboulbeniales) and 8% with Parasitylenchus 22 bifurcatus nematodes (Nematoda: Tylenchida, Allantonematidae). -
Large Positive Ecological Changes of Small Urban Greening Actions Luis Mata, Amy K. Hahs, Estibaliz Palma, Anna Backstrom, Tyler King, Ashley R
Large positive ecological changes of small urban greening actions Luis Mata, Amy K. Hahs, Estibaliz Palma, Anna Backstrom, Tyler King, Ashley R. Olson, Christina Renowden, Tessa R. Smith and Blythe Vogel WebPanel 2 Table S2.1. List of the 94 insect species that were recorded during the study. DET: Detritivore; HER: Herbivore; PRE: Predator; PAR: Parasitoid. All species are indigenous to the study area, excepting those marked with an *. Year 0 Year 1 Year 2 Year 3 Species/morphospecies Common name Family DET HER PRE PAR [2016] [2017] [2018] [2019] Hymenoptera | Apocrita Apocrita 5 Apocrita 5 Apocrita 33 Apocrita 33 Apocrita 36 Apocrita 36 Apocrita 37 Apocrita 37 Apocrita 40 Apocrita 40 Apocrita 44 Apocrita 44 Apocrita 46 Apocrita 46 Apocrita 48 Apocrita 48 Apocrita 49 Apocrita 49 Apocrita 51 Apocrita 51 Apocrita 52 Apocrita 52 Apocrita 53 Apocrita 53 Apocrita 54 Apocrita 54 Apocrita 55 Apocrita 55 Apocrita 56 Apocrita 56 Apocrita 57 Apocrita 57 Apocrita 58 Apocrita 58 Apocrita 59 Apocrita 59 Apocrita 60 Apocrita 60 Apocrita 61 Apocrita 61 Apocrita 62 Apocrita 62 Apocrita 65 Apocrita 65 Apocrita 74 Apocrita 74 Apocrita 89 Apocrita 89 Apocrita 90 Apocrita 90 Apocrita 91 Apocrita 91 Hymenoptera | Apoidea | Anthophila Anthophila 1 Anthophila 1 Anthophila 3 Anthophila 3 Apis mellifera* European honeybee Apidae Diptera | Brachycera Brachycera 2 Brachycera 2 Brachycera 7 Brachycera 7 Brachycera 8 Brachycera 8 Brachycera 14 Brachycera 14 Brachycera 15 Brachycera 15 Brachycera 16 Brachycera 16 Brachycera 18 Brachycera 18 Brachycera 19 Brachycera