Maunakea Invertebrate Threats, Identification, Collection, and Processing Guide
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San Gabriel Chestnut ESA Petition
BEFORE THE SECRETARY OF THE INTERIOR PETITION TO THE U.S. FISH AND WILDLIFE SERVICE TO PROTECT THE SAN GABRIEL CHESTNUT SNAIL UNDER THE ENDANGERED SPECIES ACT © James Bailey CENTER FOR BIOLOGICAL DIVERSITY Notice of Petition Ryan Zinke, Secretary U.S. Department of the Interior 1849 C Street NW Washington, D.C. 20240 [email protected] Greg Sheehan, Acting Director U.S. Fish and Wildlife Service 1849 C Street NW Washington, D.C. 20240 [email protected] Paul Souza, Director Region 8 U.S. Fish and Wildlife Service Pacific Southwest Region 2800 Cottage Way Sacramento, CA 95825 [email protected] Petitioner The Center for Biological Diversity is a national, nonprofit conservation organization with more than 1.3 million members and supporters dedicated to the protection of endangered species and wild places. http://www.biologicaldiversity.org Failure to grant the requested petition will adversely affect the aesthetic, recreational, commercial, research, and scientific interests of the petitioning organization’s members and the people of the United States. Morally, aesthetically, recreationally, and commercially, the public shows increasing concern for wild ecosystems and for biodiversity in general. 1 November 13, 2017 Dear Mr. Zinke: Pursuant to Section 4(b) of the Endangered Species Act (“ESA”), 16 U.S.C. §1533(b), Section 553(3) of the Administrative Procedures Act, 5 U.S.C. § 553(e), and 50 C.F.R. §424.14(a), the Center for Biological Diversity and Tierra Curry hereby formally petition the Secretary of the Interior, through the United States Fish and Wildlife Service (“FWS”, “the Service”) to list the San Gabriel chestnut snail (Glyptostoma gabrielense) as a threatened or endangered species under the Endangered Species Act and to designate critical habitat concurrently with listing. -
Winged Ants (Hymenoptera: Formicidae) Presence in Twigs on the Leaf Litter of Atlantic Forest
Biota Neotropica 19(3): e20180694, 2019 www.scielo.br/bn ISSN 1676-0611 (online edition) Inventory Winged ants (Hymenoptera: Formicidae) presence in twigs on the leaf litter of Atlantic Forest Tae Tanaami Fernandes1 , Rogério R. Silva2, Débora Rodrigues de Souza-Campana2, Otávio Guilherme Morais da Silva2 & Maria Santina de Castro Morini1* 1Universidade de Mogi das Cruzes, Laboratório de Mirmecologia do Alto Tietê, Rua Dr. Cândido Xavier de Almeida e Souza, 200, CEP 08780-911, Mogi das Cruzes, SP, Brasil 2Museu Paraense Emílio Goeldi, Coordenação de Ciências da Terra e Ecologia, Avenida Perimetral, 1901, Terra Firme, CEP 66077-830, Belém, PA, Brasil *Corresponding author: Maria Santina de Castro Morini, e-mail: [email protected] FERNANDES, T. T., SILVA, R. R., SOUZA-CAMPANA, D. R., SILVA, O. G. M., MORINI, M. S. C. Winged ants (Hymenoptera: Formicidae) presence in twigs on the leaf litter of Atlantic Forest. Biota Neotropica 19(3): e20180694. http://dx.doi.org/10.1590/1676-0611-BN-2018-0694 Abstract: In the leaf litter, ants have various nesting resources available, such as live or dead trunks, twigs, leaves, fruits and seeds. On the twigs, there are adults and immature individuals, but also the queen and winged. The production of wings requires time and energy from the colony. The objective of this study was to investigate the presence of winged in ant colonies in twigs on the leaf litter. Our prediction is that the richness and abundance of winged in twigs are the greatest in rainy months. We collected all twigs with ants in 552 plots with 16 m2, totaling 8,832 m2 of leaf litter, in areas located in the Brazilian Atlantic Domain. -
User's Guide Project: the Impact of Non-Native Predators On
User’s Guide Project: The Impact of Non-Native Predators on Pollinators and Native Plant Reproduction in a Hawaiian Dryland Ecosystem SERDP project number: RC-2432 Principal Investigators: Christina T. Liang, USDA Forest Service Clare E. Aslan, Northern Arizona University William P. Haines, University of Hawaiʻi at Mānoa Aaron B. Shiels, USDA APHIS Contributor: Manette E. Sandor, Northern Arizona University Date: 30 October 2019 Form Approved REPORT DOCUMENTATION PAGE OMB No. 0704-0188 Public reporting burden for this collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing this collection of information. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to Department of Defense, Washington Headquarters Services, Directorate for Information Operations and Reports (0704-0188), 1215 Jefferson Davis Highway, Suite 1204, Arlington, VA 22202- 4302. Respondents should be aware that notwithstanding any other provision of law, no person shall be subject to any penalty for failing to comply with a collection of information if it does not display a currently valid OMB control number. PLEASE DO NOT RETURN YOUR FORM TO THE ABOVE ADDRESS. 1. REPORT DATE (DD-MM-YYYY) 2. REPORT TYPE 3. DATES COVERED (From - To) 10-30-2019 User’s Guide 01-02-2014 to 10-30-2019 4. TITLE AND SUBTITLE 5a. CONTRACT NUMBER User’s Guide. The Impact of Non-Native Predators on Pollinators and Native Plant Reproduction in a Hawaiian Dryland Ecosystem. -
ORIGINAL ARTICLE a Novel Intracellular Mutualistic Bacterium in the Invasive Ant Cardiocondyla Obscurior
The ISME Journal (2016) 10, 376–388 © 2016 International Society for Microbial Ecology All rights reserved 1751-7362/16 www.nature.com/ismej ORIGINAL ARTICLE A novel intracellular mutualistic bacterium in the invasive ant Cardiocondyla obscurior Antonia Klein1,8, Lukas Schrader1,8, Rosario Gil2, Alejandro Manzano-Marín2, Laura Flórez3, David Wheeler5, John H Werren6, Amparo Latorre2,7, Jürgen Heinze1, Martin Kaltenpoth3,4, Andrés Moya2 and Jan Oettler1 1Institut für Zoologie, Universität Regensburg, Regensburg, Germany; 2Institut Canvanilles de Biodiversitat i Biologia Evolutiva (ICBiBE), Parc Cientific de la Universitat de Valencia, Paterna (Valencia), Spain; 3Max Planck Institute for Chemical Ecology, Jena, Germany; 4Johannes Gutenberg University Mainz, Institute for Zoology, Department for Evolutionary Ecology, Mainz, Germany; 5Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand; 6Department of Biology, University Rochester, Rochester, NY, USA and 7Área de Genómica y Salud de la Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)–Salud Pública, Valencia, Spain The evolution of eukaryotic organisms is often strongly influenced by microbial symbionts that confer novel traits to their hosts. Here we describe the intracellular Enterobacteriaceae symbiont of theinvasiveantCardiocondyla obscurior, ‘Candidatus Westeberhardia cardiocondylae’. Upon metamorphosis, Westeberhardia is found in gut-associated bacteriomes that deteriorate following eclosion. Only queens maintain Westeberhardia in the ovarian nurse cells from where the symbionts are transmitted to late-stage oocytes during nurse cell depletion. Functional analyses of the streamlined genome of Westeberhardia (533 kb, 23.41% GC content) indicate that neither vitamins nor essential amino acids are provided for the host. However, the genome encodes for an almost complete shikimate pathway leading to 4-hydroxyphenylpyruvate, which could be converted into tyrosine by the host. -
Mollusca) from Malta
The Central Mediterranean Naturalist 4 (1): 35 - 40 Malta: December 2003 ON SOME ALIEN TERRESTRIAL AND FRESHWATER GASTROPODS (MOLLUSCA) FROM MALTA Constantine Mifsud!, Paul Sammut2 and Charles Cachia3 ABSTRACT Nine species of gastropod molluscs: Otala lactea (0. F. MUller, 1774); Cemuella virgata (da Costa, 1778); Cochlicella barbara (Linnaeus, 1758); Oxychilus helveticus (Blum, 1881); Succinea putris (Linnaeus, 1758); Oxyloma elegans (Risso, 1826); Helisoma duryi Wetherby, 1879; Planorbarius comeus (Linnaeus, 1758); and the limacid slug Lehmannia valentiana (A. Ferussac, 1822) are recorded for the first time as alien species from local plant nurseries. For each species a short description and notes on distribution and ecology are given. INTRODUCTION The land and fresh water Mollusca of the Maltese Islands have been recently well treated by Giusti et al. (1995). However, during the last twelve years many non-indigenous plants, shrubs and trees, both decorative species and fruit trees, have been imported from Europe either to embellish local gardens or roadsides or for agricultural purposes. It occurred to the authors that there is the possibility that alien species of molluscs might have been introduced accidentally with these imported plants. This is not a completely new phenomenon. For example, Pomatias elegans and Discus rotundatus occur at San Anton Gardens were they were probably alien introductions due to human activities (Thake, 1973). During recent research to assess the status of some of the endemic molluscs of the Maltese Islands, with special emphasis on the Limacidae, areas where imported plants are stocked were searched for any alien species. This resulted in the discovery of several alien species of terrestrial and freshwater snails, a few of them alive. -
Coleoptera: Coccinellidae) in Illinois, U.S.A., and Relation to Its Other Midwestern Collection Records
The Great Lakes Entomologist Volume 50 Numbers 1 & 2 -- Spring/Summer 2017 Article 9 Numbers 1 & 2 -- Spring/Summer 2017 September 2017 First Record of Hippodamia variegata (Coleoptera: Coccinellidae) in Illinois, U.S.A., and Relation to Its Other Midwestern Collection Records Louis S. Hesler USDA-ARS North Central Agricultural Research Laboratory, Brookings, SD, [email protected] Jonathan G. Lundgren Ecdysis Foundation Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Hesler, Louis S. and Lundgren, Jonathan G. 2017. "First Record of Hippodamia variegata (Coleoptera: Coccinellidae) in Illinois, U.S.A., and Relation to Its Other Midwestern Collection Records," The Great Lakes Entomologist, vol 50 (1) Available at: https://scholar.valpo.edu/tgle/vol50/iss1/9 This Scientific Note is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. First Record of Hippodamia variegata (Coleoptera: Coccinellidae) in Illinois, U.S.A., and Relation to Its Other Midwestern Collection Records Cover Page Footnote This research was supported by funding through USDA-ARS CRIS Project Number 3080-21220-006-00D. Eric Beckendorf assisted in collection maintenance. Al Wheeler, Mathew Brust, Lauren Hesler and Eric Beckendorf graciously reviewed drafts of this paper. This scientific note is va ailable in The Great Lakes Entomologist: https://scholar.valpo.edu/tgle/vol50/iss1/9 Hesler and Lundgren: Hippodamia variegata in Illinois 2017 THE GREAT LAKES ENTOMOLOGIST 43 First Record of Hippodamia variegata (Coleoptera: Coccinellidae) in Illinois, U.S.A., and Relation to Its Other Midwestern Collection Records Louis S. -
Managing Alternative Pollinators a Handbook for Beekeepers, Growers, and Conservationists
Managing Alternative Pollinators A Handbook for Beekeepers, Growers, and Conservationists ERIC MADER • MARLA SPIVAK • ELAINE EVANS Fair Use of this PDF file of Managing Alternative Pollinators: A Handbook for Beekeepers, Growers, and Conservationists, SARE Handbook 11, NRAES-186 By Eric Mader, Marla Spivak, and Elaine Evans Co-published by SARE and NRAES, February 2010 You can print copies of the PDF pages for personal use. If a complete copy is needed, we encourage you to purchase a copy as described below. Pages can be printed and copied for educational use. The book, authors, SARE, and NRAES should be acknowledged. Here is a sample acknowledgement: ----From Managing Alternative Pollinators: A Handbook for Beekeepers, Growers, and Conservationists, SARE Handbook 11, by Eric Mader, Marla Spivak, and Elaine Evans, and co- published by SARE and NRAES.---- No use of the PDF should diminish the marketability of the printed version. If you have questions about fair use of this PDF, contact NRAES. Purchasing the Book You can purchase printed copies on NRAES secure web site, www.nraes.org, or by calling (607) 255-7654. The book can also be purchased from SARE, visit www.sare.org. The list price is $23.50 plus shipping and handling. Quantity discounts are available. SARE and NRAES discount schedules differ. NRAES PO Box 4557 Ithaca, NY 14852-4557 Phone: (607) 255-7654 Fax: (607) 254-8770 Email: [email protected] Web: www.nraes.org SARE 1122 Patapsco Building University of Maryland College Park, MD 20742-6715 (301) 405-8020 (301) 405-7711 – Fax www.sare.org More information on SARE and NRAES is included at the end of this PDF. -
The Genetic Mechanism of Selfishness and Altruism in Parent-Offspring Coadaptation Min Wu, Jean-Claude Walser, Lei Sun and Mathias Kölliker
SCIENCE ADVANCES | RESEARCH ARTICLE EVOLUTIONARY BIOLOGY Copyright © 2020 The Authors, some rights reserved; The genetic mechanism of selfishness and altruism exclusive licensee American Association in parent-offspring coadaptation for the Advancement Min Wu1*, Jean-Claude Walser2, Lei Sun3†, Mathias Kölliker1*‡ of Science. No claim to original U.S. Government Works. Distributed The social bond between parents and offspring is characterized by coadaptation and balance between altruistic under a Creative and selfish tendencies. However, its underlying genetic mechanism remains poorly understood. Using transcriptomic Commons Attribution screens in the subsocial European earwig, Forficula auricularia, we found the expression of more than 1600 genes License 4.0 (CC BY). associated with experimentally manipulated parenting. We identified two genes, Th and PebIII, each showing evidence of differential coexpression between treatments in mothers and their offspring. In vivo RNAi experiments confirmed direct and indirect genetic effects of Th and PebIII on behavior and fitness, including maternal food provisioning and reproduction, and offspring development and survival. The direction of the effects consistently indicated a reciprocally altruistic function for Th and a reciprocally selfish function for PebIII. Further metabolic pathway analyses suggested roles for Th-restricted endogenous dopaminergic reward, PebIII-mediated chemical communication and a link to insulin signaling, juvenile hormone, and vitellogenin in parent-offspring Downloaded from coadaptation and social evolution. INTRODUCTION manipulations with and without mother-offspring contact, without Parents and offspring influence each other’s behavior and evolutionary detrimental effects on offspring. Females produce one or two clutches http://advances.sciencemag.org/ fitness through reciprocal interactions (1). As an altruistic trait, over their lifetime and provide food (see movie S1) and protection parental care is beneficial to the survival and development of offspring to their young nymphs (8, 9). -
Hippodamia Variegata (Goeze) (Coleoptera: Coccinellidae) Detected in Michigan Soybean Fields
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by ValpoScholar The Great Lakes Entomologist Volume 38 Numbers 3 & 4 - Fall/Winter 2005 Numbers 3 & Article 8 4 - Fall/Winter 2005 October 2005 Hippodamia Variegata (Goeze) (Coleoptera: Coccinellidae) Detected in Michigan Soybean Fields Mary M. Gardiner Michigan State University Gary L. Parsons Michigan State University Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Gardiner, Mary M. and Parsons, Gary L. 2005. "Hippodamia Variegata (Goeze) (Coleoptera: Coccinellidae) Detected in Michigan Soybean Fields," The Great Lakes Entomologist, vol 38 (2) Available at: https://scholar.valpo.edu/tgle/vol38/iss2/8 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Gardiner and Parsons: <i>Hippodamia Variegata</i> (Goeze) (Coleoptera: Coccinellidae) D 164 THE GREAT LAKES ENTOMOLOGIST Vol. 38, Nos. 3 & 4 HIPPODAMIA VARIEGATA (GOEZE) (COLEOPTERA: COCCINELLIDAE) DETECTED IN MICHIGAN SOYBEAN FIELDS Mary M. Gardiner1 and Gary L. Parsons2 ABSTRACT Since its initial detection near Montreal, Canada in 1984, the variegated lady beetle Hippodamia variegata (Goeze) (Coleoptera:Coccinellidae) has spread throughout the northeastern United States. In 2005, this immigrant Old World species was detected in Michigan for the first time. Twenty-nine adults were found in soybean fields in 4 counties: Ingham, Gratiot, Kalamazoo, and Saginaw. -
The Slugs of Bulgaria (Arionidae, Milacidae, Agriolimacidae
POLSKA AKADEMIA NAUK INSTYTUT ZOOLOGII ANNALES ZOOLOGICI Tom 37 Warszawa, 20 X 1983 Nr 3 A n d rzej W ik t o r The slugs of Bulgaria (A rionidae , M ilacidae, Limacidae, Agriolimacidae — G astropoda , Stylommatophora) [With 118 text-figures and 31 maps] Abstract. All previously known Bulgarian slugs from the Arionidae, Milacidae, Limacidae and Agriolimacidae families have been discussed in this paper. It is based on many years of individual field research, examination of all accessible private and museum collections as well as on critical analysis of the published data. The taxa from families to species are sup plied with synonymy, descriptions of external morphology, anatomy, bionomics, distribution and all records from Bulgaria. It also includes the original key to all species. The illustrative material comprises 118 drawings, including 116 made by the author, and maps of localities on UTM grid. The occurrence of 37 slug species was ascertained, including 1 species (Tandonia pirinia- na) which is quite new for scientists. The occurrence of other 4 species known from publications could not bo established. Basing on the variety of slug fauna two zoogeographical limits were indicated. One separating the Stara Pianina Mountains from south-western massifs (Pirin, Rila, Rodopi, Vitosha. Mountains), the other running across the range of Stara Pianina in the^area of Shipka pass. INTRODUCTION Like other Balkan countries, Bulgaria is an area of Palearctic especially interesting in respect to malacofauna. So far little investigation has been carried out on molluscs of that country and very few papers on slugs (mostly contributions) were published. The papers by B a b o r (1898) and J u r in ić (1906) are the oldest ones. -
Arthropod Diversity Estimates for Three Native Subalpine Plant
ARTHROPOD DIVERSITY ESTIMATES FOR THREE NATIVE SUBALPINE PLANT SPECIES ON THE MAUNAKEA VOLCANO OF HAWAI‘I ISLAND A THESIS SUBMITTED TO THE GRADUATE DIVISION OF THE UNIVERSITY OF HAWAI‘I AT HILO IN PARTIAL FULFULLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE IN TROPICAL CONSERVATION BIOLOGY AND ENVIRONMENTAL SCIENCE DECEMBER 2016 By Heather Stever Thesis Committee: Jesse Eiben, Chairperson Ryan Perroy Paul Selmants Keywords: Arthropods, Endemic, Hawai‘i, Insects, Maunakea, Subalpine Acknowledgements I am immensely grateful for the knowledge, advice, support, and funding that I received from the many people and organizations that helped to make this project possible. I would like to especially thank my academic advisor, Jesse Eiben, the University of Hawai‘i at Hilo Office of Maunakea Management, and the Tropical Conservation Biology and Environmental Science faculty and students. I would also like to thank, in alphabetical order, Nina Buchanan, Jessica Kirkpatrick, Frederick Klasner, Devin Leopold, Stephanie Nagata, Julien Pétillon, Ryan Perroy, Daniel Rubinoff, Esther Sebastián-González, Paul Selmants, Marleena Sheffield, Michael Shintaku, Andrew Stever, Amber Stillman, and Darcy Yogi. ii Abstract Terrestrial arthropods are among the most abundant and diverse animals on Earth, especially in Hawai‘i where they constitute the vast majority of endemic fauna and play crucial roles in nearly every habitat throughout the islands. Arthropod surveys and inventories are useful methods for documenting arthropod diversity, but studying arthropods can be extremely difficult. Arthropod collection is often taxing because many species are very mobile and exist in harsh climates or on terrain that is difficult to access. Arthropod identification can also be challenging since many arthropods are remarkably small with complex morphologies and diverse life histories. -
Genomes of the Hymenoptera Michael G
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital Repository @ Iowa State University Ecology, Evolution and Organismal Biology Ecology, Evolution and Organismal Biology Publications 2-2018 Genomes of the Hymenoptera Michael G. Branstetter U.S. Department of Agriculture Anna K. Childers U.S. Department of Agriculture Diana Cox-Foster U.S. Department of Agriculture Keith R. Hopper U.S. Department of Agriculture Karen M. Kapheim Utah State University See next page for additional authors Follow this and additional works at: https://lib.dr.iastate.edu/eeob_ag_pubs Part of the Behavior and Ethology Commons, Entomology Commons, and the Genetics and Genomics Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ eeob_ag_pubs/269. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Ecology, Evolution and Organismal Biology at Iowa State University Digital Repository. It has been accepted for inclusion in Ecology, Evolution and Organismal Biology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Genomes of the Hymenoptera Abstract Hymenoptera is the second-most sequenced arthropod order, with 52 publically archived genomes (71 with ants, reviewed elsewhere), however these genomes do not capture the breadth of this very diverse order (Figure 1, Table 1). These sequenced genomes represent only 15 of the 97 extant families. Although at least 55 other genomes are in progress in an additional 11 families (see Table 2), stinging wasps represent 35 (67%) of the available and 42 (76%) of the in progress genomes.