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Elizabeth I. Cash
ELIZABETH I. CASH Department of Environmental Science, Policy, and Management University of California, Berkeley 130 Mulford Hall, #3114 Berkeley, CA 94720-3114 Email: [email protected] URL: http://www.elizabethcash.com/ CURRENT POSITION University of California, Berkeley Berkeley, CA Postdoctoral Scholar August 2016 - Present EDUCATION Arizona State University Tempe, AZ PhD, Biology 2016 Dissertation: Proximate and ultimate mechanisms of nestmate recognition in ants Advisors: Jürgen Gadau (committee chair) & Jürgen Liebig Committee: Jennifer Fewell, Bert Hölldobler, & Kenro Kusumi The Ohio State University Columbus, OH BSc, cum laude, Biology 2009 Independent Research: The function of pheromones in socially parasitic Lasius ants Advisors: Joseph Raczkowski, Steven Rissing, & John Wenzel University of Cincinnati Cincinnati, OH Foundation Coursework, Design 1999 RESEARCH EXPERIENCE AND TRAINING University of California, Berkeley Berkeley, CA Postdoctoral Scholar; Advisor: Neil D. Tsutsui August 2016 - Present Evolution of desiccation resistance and colony recognition in Argentine ants Arizona State University Tempe, AZ Graduate Research Associate; Advisor: Jürgen Gadau 2009 - 2016 Acyl-CoA desaturase gene family evolution and function in ants Ant Course Portal, AZ Participant; Field course on ant collection, identification, and curation 2015 University of Würzburg / Arizona State University Würzburg, Germany Participant; International symposium and workshop on frontiers in insect biology 2014 Smithsonian Tropical Research Institute / Arizona State University BCI, Panama Participant; Tropical Field Biology course 2011 The Ohio State University Columbus, OH Laboratory Assistant; Advisors: Joseph Raczkowski, Steven Rissing, & John Wenzel 2007 - 2009 Behavioral and chemical ecology of social parasitism in Lasius ants 1 PEER-REVIEWED PUBLICATIONS Cash E, Tsutsui N, and Smith A (in preparation) The evolution of acyl-CoA desaturase genes in Odontomachus trap-jaw ants. -
The Functions and Evolution of Social Fluid Exchange in Ant Colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C
ISSN 1997-3500 Myrmecological News myrmecologicalnews.org Myrmecol. News 31: 1-30 doi: 10.25849/myrmecol.news_031:001 13 January 2021 Review Article Trophallaxis: the functions and evolution of social fluid exchange in ant colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C. LeBoeuf Abstract Trophallaxis is a complex social fluid exchange emblematic of social insects and of ants in particular. Trophallaxis behaviors are present in approximately half of all ant genera, distributed over 11 subfamilies. Across biological life, intra- and inter-species exchanged fluids tend to occur in only the most fitness-relevant behavioral contexts, typically transmitting endogenously produced molecules adapted to exert influence on the receiver’s physiology or behavior. Despite this, many aspects of trophallaxis remain poorly understood, such as the prevalence of the different forms of trophallaxis, the components transmitted, their roles in colony physiology and how these behaviors have evolved. With this review, we define the forms of trophallaxis observed in ants and bring together current knowledge on the mechanics of trophallaxis, the contents of the fluids transmitted, the contexts in which trophallaxis occurs and the roles these behaviors play in colony life. We identify six contexts where trophallaxis occurs: nourishment, short- and long-term decision making, immune defense, social maintenance, aggression, and inoculation and maintenance of the gut microbiota. Though many ideas have been put forth on the evolution of trophallaxis, our analyses support the idea that stomodeal trophallaxis has become a fixed aspect of colony life primarily in species that drink liquid food and, further, that the adoption of this behavior was key for some lineages in establishing ecological dominance. -
Comparison of Coleoptera Emergent from Various Decay Classes of Downed Coarse Woody Debris in Great Smoky Mountains National Park, USA
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 11-30-2012 Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains National Park, USA Michael L. Ferro Louisiana State Arthropod Museum, [email protected] Matthew L. Gimmel Louisiana State University AgCenter, [email protected] Kyle E. Harms Louisiana State University, [email protected] Christopher E. Carlton Louisiana State University Agricultural Center, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Ferro, Michael L.; Gimmel, Matthew L.; Harms, Kyle E.; and Carlton, Christopher E., "Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains National Park, USA" (2012). Insecta Mundi. 773. https://digitalcommons.unl.edu/insectamundi/773 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA A Journal of World Insect Systematics MUNDI 0260 Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains Na- tional Park, USA Michael L. Ferro Louisiana State Arthropod Museum, Department of Entomology Louisiana State University Agricultural Center 402 Life Sciences Building Baton Rouge, LA, 70803, U.S.A. [email protected] Matthew L. Gimmel Division of Entomology Department of Ecology & Evolutionary Biology University of Kansas 1501 Crestline Drive, Suite 140 Lawrence, KS, 66045, U.S.A. -
Hox-Logic of Body Plan Innovations for Social Symbiosis in Rove Beetles
bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 Hox-logic of body plan innovations for social symbiosis in rove beetles 2 3 Joseph Parker1*, K. Taro Eldredge2, Isaiah M. Thomas3, Rory Coleman4 and Steven R. Davis5 4 5 1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, 6 CA 91125, USA 7 2Department of Ecology and Evolutionary Biology, and Division of Entomology, Biodiversity 8 Institute, University of Kansas, Lawrence, KS, USA 9 3Department of Genetics and Development, Columbia University, 701 West 168th Street, New 10 York, NY 10032, USA 11 4Laboratory of Neurophysiology and Behavior, The Rockefeller University, New York, NY 10065, 12 USA 13 5Division of Invertebrate Zoology, American Museum of Natural History, New York, NY 10024, 14 USA 15 *correspondence: [email protected] 16 17 18 19 20 21 22 23 24 25 26 27 1 bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 How symbiotic lifestyles evolve from free-living ecologies is poorly understood. In 2 Metazoa’s largest family, Staphylinidae (rove beetles), numerous lineages have evolved 3 obligate behavioral symbioses with ants or termites. -
Phylogeny and Evolution of Myrmecophily in Beetles, Based on Morphological Evidence (Coleoptera: Ptinidae, Scarabaeidae)
Phylogeny and Evolution Of Myrmecophily In Beetles, Based On Morphological Evidence (Coleoptera: Ptinidae, Scarabaeidae) DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Glené Mynhardt Graduate Program in Evolution, Ecology and Organismal Biology The Ohio State University 2012 Dissertation Committee: Johannes Klompen, Advisor Marymegan Daly Norman Johnson T. Keith Philips Copyright by Glené Mynhardt 2012 Abstract Ant-associated behavior has evolved rampantly among various groups of Arthropoda, and has arisen in at least 34 families of beetles. Due to the amazing morphological modifications and different kinds of interactions that occur within myrmecophilous (ant-associated) beetles, authors have predicted that myrmecophily has evolved in a step-wise fashion from casual, facultative associations to closely integrated, obligate interactions. In this dissertation, myrmecophily within the Coleoptera is reviewed, and known behaviors, ant-beetle interactions, and associated morphological adaptations are discussed. In order to better understand how myrmecophily has evolved, two groups of beetles are studied in a phylogenetic context. A cladistic analysis of 40 species of the myrmecophilous scarab genus, Cremastocheilu s Knoch is presented. Characters related to a myrmecophilous habit are largely informative, especially those characters related to the glandular trichomes (clusters of setae typically associated with exocrine glands). Two of the five previously recognized subgenera, C. (Myrmecotonus ) and C. (Anatrinodia ) are synonymized with the subgenus C. (Cremastocheilus ). Even though behavioral information is only known for a few species, the resulting phylogeny indicates that monophyletic subgenera are largely associated with the same ant hosts, although specific interactions with ant hosts can vary even in closely-related taxa. -
Hox-Logic of Preadaptations for Social Insect Symbiosis in Rove Beetles
bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. All rights reserved. No reuse allowed without permission. Hox-logic of preadaptations for social insect symbiosis in rove beetles Joseph Parker1*, K. Taro Eldredge2, Isaiah M. Thomas3, Rory Coleman3 and Steven R. Davis3,4 1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA 2Department of Ecology and Evolutionary Biology, and Division of Entomology, Biodiversity Institute, University of Kansas, Lawrence, KS, USA 3Department of Genetics and Development, Columbia University, 701 West 168th Street, New York, NY 10032, USA 4Division of Invertebrate Zoology, American Museum of Natural History, New York, NY 10024, USA *correspondence: [email protected] bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. All rights reserved. No reuse allowed without permission. How symbiotic lifestyles evolve from free-living ecologies is poorly understood. Novel traits mediating symbioses may stem from preadaptations: features of free- living ancestors that predispose taxa to engage in nascent interspecies relationships. In Metazoa’s largest family, Staphylinidae (rove beetles), the body plan within the subfamily Aleocharinae is preadaptive for symbioses with social insects. Short elytra expose a pliable abdomen that bears targetable glands for host manipulation or chemical defense. The exposed abdomen has also been convergently refashioned into ant- and termite-mimicking shapes in multiple symbiotic lineages. Here we show how this preadaptive anatomy evolved via novel Hox gene functions that remodeled the ancestral coleopteran groundplan. -
From Socotra Island
ACTA ENTOMOLOGICA MUSEI NATIONALIS PRAGAE Published 30.xii.2014 Volume 54 (supplementum), pp. 121–132 ISSN 0374-1036 http://zoobank.org/urn:lsid:zoobank.org:pub:074A670B-274F-4E51-8C73-D44BF76347C8 A review of the Pselaphinae (Coleoptera: Staphylinidae) from Socotra Island Peter HLAVÁČ1) & Petr BAŇAŘ2) 1) Czech University of Life Sciences Prague, Faculty of Forestry and Wood Sciences, Department of Forest Protection and Game Management, Kamýcká 1176, CZ-165 21 Praha 6–Suchdol, Czech Republic; e-mail: [email protected] 2) Moravian Museum, Department of Entomology, Hviezdoslavova 29a, Brno, CZ-627 00, Czech Republic; e-mail: [email protected] Abstract. First records of the Pselaphinae (Staphylinidae) from Socotra Island, Yemen, are given. Three new species: Epicaris bezdeki sp. nov., Trissemus so- cotranus sp. nov. and Centrophthalmus scanticola sp. nov. are described. A new diagnosis of the genus Epicaris Reitter, 1882 is provided and a redescription is also given. The list of the Pselaphinae of Socotra Island is completed by records of Articerodes syriacus (Saulcy, 1865), Ctenisomorphus major (Raffray, 1877), and Trissemus maroccanus wittmeri Besuchet, 1981. Key words. Coleoptera, Staphylinidae, Pselaphinae, Centrophthalmus, Epicaris, Trissemus, taxonomy, new species, new records, Yemen, Socotra Introduction Socotra is relatively large island in the Indian Ocean, lying some 240 kilometres east of the Horn of Africa and 380 kilometres south of the Arabian Peninsula. The island is very isolated with a high level of endemism, e.g., a third of its plant life is found nowhere else on the planet (for review see BATELKA 2012). The beetle fauna of the island is very poorly known in general (cf. -
Aquatic Insects: Bryophyte Habitats and Fauna
Glime, J. M. 2017. Aquatic Insects: Bryophyte Habitats and Fauna. Chapt. 11-3. In: Glime, J. M. Bryophyte Ecology. Volume 2. 11-3-1 Bryological Interaction. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 19 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 11-3 AQUATIC INSECTS: BRYOPHYTE HABITATS AND FAUNA TABLE OF CONTENTS Aquatic Bryophyte Habitat and Fauna ..................................................................................................................... 11-3-2 Streams .............................................................................................................................................................. 11-3-4 Streamside ......................................................................................................................................................... 11-3-7 Artificial Bryophytes ......................................................................................................................................... 11-3-7 Preference Experiment ...................................................................................................................................... 11-3-8 Torrents and waterfalls ...................................................................................................................................... 11-3-9 Springs ............................................................................................................................................................. -
Coleoptera: Staphylinidae)
University of New Hampshire University of New Hampshire Scholars' Repository New Hampshire Agricultural Experiment Station Publications New Hampshire Agricultural Experiment Station 6-1999 New Synonymies and Combinations for New World Pselaphinae (Coleoptera: Staphylinidae) Donald S. Chandler University of New Hampshire, [email protected] Follow this and additional works at: https://scholars.unh.edu/nhaes Part of the Entomology Commons Recommended Citation New Synonymies and Combinations for New World Pselaphinae (Coleoptera: Staphylinidae) Donald S. Chandler Transactions of the American Entomological Society (1890-) Vol. 125, No. 1/2 (Jun., 1999) , pp. 163-183 Published by: American Entomological Society Stable URL: http://www.jstor.org/stable/ 25078677 This Article is brought to you for free and open access by the New Hampshire Agricultural Experiment Station at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in New Hampshire Agricultural Experiment Station Publications by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. New Synonymies and Combinations for New World Pselaphinae (Coleoptera: Staphylinidae) Author(s): Donald S. Chandler Source: Transactions of the American Entomological Society (1890-), Vol. 125, No. 1/2 (Jun., 1999), pp. 163-183 Published by: American Entomological Society Stable URL: http://www.jstor.org/stable/25078677 . Accessed: 04/02/2015 14:56 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. -
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INSECTA A Journal of World Insect Systematics MUNDI 0277 A complete checklist with new records and geographical distribution of the rove beetles (Coleoptera, Staphylinidae) of Brazil Angélico Asenjo Laboratório de Sistemática e Bioecologia de Coleoptera (Insecta), Departamento de Zoologia, Universidade Federal do Paraná, Caixa Postal 19020, CEP. 81531–980 Curitiba, Paraná, Brazil [email protected] Ulrich Irmler Department of Applied Ecology, Institute for Ecosystem Research, Christian Albrecht University, 24098 Kiel, Germany [email protected] Jan Klimaszewski Natural Resources Canada, Canadian Forest Service, 1055 du P.E.P.S., P.O. Box 10380, Stn. Sainte-Foy, Québec, Quebec, Canada G1V 4C7 [email protected] Lee H. Herman American Museum of Natural History, Division of Invertebrate Zoology, Central Park West at 79th Street, New York, New York 10024, USA [email protected] Donald S. Chandler Department of Biological Sciences University of New Hampshire Durham, NH 03824, USA [email protected] Date of Issue: February 15, 2013 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Angélico Asenjo, Ulrich Irmler, Jan Klimaszewski, Lee H. Herman, Donald S. Chandler A complete checklist with new records and geographical distribution of the rove beetles (Coleoptera, Staphylinidae) of Brazil Insecta Mundi 0277: 1–419 ZooBank Registered urn:lsid:zoobank.org:pub:5D7FEEAC-9B8E-4C00-B78B-D4A379EA0925 Published in 2013 by Center for Systematic Entomology, Inc. P. O. Box 141874 Gainesville, FL 32614-1874 USA http://www.centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non-marine arthropod. Topics considered for publication include systematics, taxonomy, nomenclature, checklists, faunal works, and natural history. -
(Coleoptera: Staphylinidae) of South Carolina, Based on Published Records
The Coleopterists Bulletin, 71(3): 513–527. 2017. ACHECKLIST OF THE ROVE BEETLES (COLEOPTERA:STAPHYLINIDAE) OF SOUTH CAROLINA,BASED ON PUBLISHED RECORDS MICHAEL S. CATERINO AND MICHAEL L. FERRO Clemson University Arthropod Collection Department of Plant and Environmental Sciences 277 Poole Agricultural Center, Clemson University Clemson, SC 29634-0310, USA [email protected], [email protected] ABSTRACT A review of the literature revealed 17 subfamilies and 355 species of rove beetles (Staphylinidae) reported from South Carolina. Updated nomenclature and references are provided for all species. The goal of this list is to set a baseline for improvement of our knowledge of the state’s staphylinid fauna, as well as to goad ourselves and others into creating new, or updating existing, regional faunal lists of the world’s most speciose beetle family. Key Words: checklist, regional fauna, biodiversity, Nearctic DOI.org/10.1649/0010-065X-71.3.513 Staphylinidae, the rove beetles, are a megadiverse South Carolina is a rather small, yet diverse state, family of beetles containing more than 62,000 de- ranging from low-lying coastal habitats through a scribed species worldwide. The family is found in variety of mid-elevation communities to montane virtually all terrestrial habitats except in the extreme areas encompassing some of the diversity of higher polar regions. It is the most diverse family across all Appalachia. The easternmost portion of the state is animal groups. Within the Nearctic region (non- within the Atlantic Coastal Plain, a recently rec- tropical North America), about 4,500 species are ognized biodiversity hotspot (Noss 2016) that in- known (Newton et al. -
A Catalog of the Coleóptera of America North of Mexico Family: Pselaphidae
A CATALOG OF THE COLEÓPTERA OF AMERICA NORTH OF MEXICO FAMILY: PSELAPHIDAE ah52931 /^^ UNITED STATES AGRICULTURE PREPARED BY fiJUl DEPARTMENT OF HANDBOOK AGRICULTURAL "^^7 AGRICULTURE NUMBER 529-31 RESEARCH SERVICE FAMILIES OF COLEóPTERA IN AMERICA NORTH OF MEXICO Fascicy Family Year issued Fascicle^ Family Year issued Fascicle^ Family Year issued 1 Cupedidae 1979 46 Callirhipidae 102 Biphyllidae 2 Micromalthidae 1982 47 Heteroceiidae 1978 103 Byturidae 1991 3 Carabidae 48 Limnichidae 1986 104 Mycetophagidae 4 Rhysodidae 1985 49 Dryopidae 1983 105 ....... Ciidae 1982 5 Amphizoidae 1984 50 Elmidae 1983 107 Prostomidae 6 Haliplidae 51 Buprestidae 109 Colydiidae 8 Noteridae 52 Cebrionidae 110....... Monommatidae 9 Dytiscidae 53 Elateridae Ill Cephaloidae 10 Gyrinidae 54 Throscidae 112 Zopheridae 13 Sphaeriidae 55....... Cerophytidae 115 ....... Tenebrionidae 14 Hydroscaphidae 56 Perothopidae 116 AUeculidae 15 Hydraenidae 57 Eucnemidae 117 Lagriidae 16 Hydrophilidae 58 Telegeusidae 118 Salpingidae ^ 17 Georyssidae 61 Phengodidae 119....... Mycteridae 18 Sphaeritidae 62 Lampyridae 120 Pyrochroidae 1983 20 Histeridae 63 ]. Cantharidae 121 Othniidae 21 Ptiliidae 64 Lycidae 122....... Inopeplidae 22 Limulodidae.. 65 Derodontidae 1989 123 Oedemeridae 23 Dasyceridae ..... 66 Nosodendridae 124 Melandryidae 24 Micropeplidae 1984 67 Dennestidae 125 Mordellidae 1986 25 .'. Leptinidae 69 Ptinidae 126 Rhipiphoridae 26 Leiodidae 70 Anobiidae 1982 127 ....... Meloidae 27 Scydmaenidae 71 Bostrichidae 128 ....... Anthicidae 28 Silphidae 1993 72 Lyctidae 129 Pedilidae 29 Scaphidiidae 74 Trogositidae 130 Euglenidae 30 Staphylinidae 76 Cleridae 131 Cerambycidae 31 Pselaphidae 1997 78 Melyridae 132 Bruchidae 32 Lucanidae 79 Lymexylidae 133 Chrysomelidae 33 Passalidae 81 Sphindidae 134 Nemonychidae 1994 34 Scarabaeidae 1984 82 Nitidulidae 135 Anthribidae 35 Eucinetidae 83 Rhizophagidae 138 AUocorynidae 1991 36 Helodidae 86 Cucujidae 140 Brentidae 37 Clambidae r....