In Memoriam: Michael C
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Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea
Brigham Young University BYU ScholarsArchive Theses and Dissertations 2018-07-01 Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco Brigham Young University Follow this and additional works at: https://scholarsarchive.byu.edu/etd Part of the Life Sciences Commons BYU ScholarsArchive Citation Pacheco, Yelena Marlese, "Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea" (2018). Theses and Dissertations. 7444. https://scholarsarchive.byu.edu/etd/7444 This Thesis is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco A thesis submitted to the faculty of Brigham Young University in partial fulfillment of the requirements for the degree of Master of Science Michael F. Whiting, Chair Sven Bradler Seth M. Bybee Steven D. Leavitt Department of Biology Brigham Young University Copyright © 2018 Yelena Marlese Pacheco All Rights Reserved ABSTRACT Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco Department of Biology, BYU Master of Science Phasmatodea exhibit a variety of cryptic ecomorphs associated with various microhabitats. Multiple ecomorphs are present in the stick insect fauna from Papua New Guinea, including the tree lobster, spiny, and long slender forms. While ecomorphs have long been recognized in phasmids, there has yet to be an attempt to objectively define and study the evolution of these ecomorphs. -
Succession of Coleoptera on Freshly Killed
Louisiana State University LSU Digital Commons LSU Master's Theses Graduate School 2008 Succession of Coleoptera on freshly killed loblolly pine (Pinus taeda L.) and southern red oak (Quercus falcata Michaux) in Louisiana Stephanie Gil Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_theses Part of the Entomology Commons Recommended Citation Gil, Stephanie, "Succession of Coleoptera on freshly killed loblolly pine (Pinus taeda L.) and southern red oak (Quercus falcata Michaux) in Louisiana" (2008). LSU Master's Theses. 1067. https://digitalcommons.lsu.edu/gradschool_theses/1067 This Thesis is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Master's Theses by an authorized graduate school editor of LSU Digital Commons. For more information, please contact [email protected]. SUCCESSIO OF COLEOPTERA O FRESHLY KILLED LOBLOLLY PIE (PIUS TAEDA L.) AD SOUTHER RED OAK ( QUERCUS FALCATA MICHAUX) I LOUISIAA A Thesis Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Master of Science in The Department of Entomology by Stephanie Gil B. S. University of New Orleans, 2002 B. A. University of New Orleans, 2002 May 2008 DEDICATIO This thesis is dedicated to my parents who have sacrificed all to give me and my siblings a proper education. I am indebted to my entire family for the moral support and prayers throughout my years of education. My mother and Aunt Gloria will have several extra free hours a week now that I am graduating. -
Ataenius Heinekeni Wollatson, 1894 (Insecta: Coleoptera: Aphodiinae)
(A. heinekeni) Ataenius heinekeni Wollatson, 1894 (Insecta: Coleoptera: Aphodiinae) By: Edrick Lugo Millán & Verónica Acevedo Ramírez, Juliana Cardona, Nico Franz Geographic Range: Bahamas (Andros), Barbados (probably introduced), Cuba, Hispaniola, Puerto Rico (Quebradillas- east of Lago Guajataca, Bayamón, Mayagüez), St. Thomas. USA (SC-FLTX), Mexico to Brazil, introduced to Ascension and Madeira islands. Habitat: A. heinekeni beetles were beaten from leaves, collected under leaves and logs on hard ground, under live-oak trees, on old rice-field dams, under roadside debris and at coastal coppice trap. (Jerath,1960). They are mainly found in animal dung and decaying material. Physical Description: Ataenius is distinguished from other genera of the Eupariini by a combination of characters, among them head narrower than pronotum, anterior clypeus visible from above, pronotum laterally without denticles and at most sparsely to moderately ciliate, sides of pronotum not explanate, elytra often with basal margination, front tibiae with slanted anterior margin, middle and hind tibiae not flattened, uniformly wider from base, hind tibiae straight with outer apical angle spiniformly prolonged, tarsi normal with first segment often as long as the following three segments combined (SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY, no 154). Length 4.3.-5.5 mm. Usually reddish-brown to black, few with color patterns, some dorsally setose.. Head moderately convex, surface smooth, granulate, wrinkled, or rugose. Abdominal fluting is distinct. External sexual dimorphisms are subtle, if present. Life Stages: The life cycle of Ataenius beetles is not well known but apparently they are humus feeders in the soil, with a few species attracted to decaying vegetation and to animal dung. -
Jordan Beans RA RMO Dir
Importation of Fresh Beans (Phaseolus vulgaris L.), Shelled or in Pods, from Jordan into the Continental United States A Qualitative, Pathway-Initiated Risk Assessment February 14, 2011 Version 2 Agency Contact: Plant Epidemiology and Risk Analysis Laboratory Center for Plant Health Science and Technology United States Department of Agriculture Animal and Plant Health Inspection Service Plant Protection and Quarantine 1730 Varsity Drive, Suite 300 Raleigh, NC 27606 Pest Risk Assessment for Beans from Jordan Executive Summary In this risk assessment we examined the risks associated with the importation of fresh beans (Phaseolus vulgaris L.), in pods (French, green, snap, and string beans) or shelled, from the Kingdom of Jordan into the continental United States. We developed a list of pests associated with beans (in any country) that occur in Jordan on any host based on scientific literature, previous commodity risk assessments, records of intercepted pests at ports-of-entry, and information from experts on bean production. This is a qualitative risk assessment, as we express estimates of risk in descriptive terms (High, Medium, and Low) rather than numerically in probabilities or frequencies. We identified seven quarantine pests likely to follow the pathway of introduction. We estimated Consequences of Introduction by assessing five elements that reflect the biology and ecology of the pests: climate-host interaction, host range, dispersal potential, economic impact, and environmental impact. We estimated Likelihood of Introduction values by considering both the quantity of the commodity imported annually and the potential for pest introduction and establishment. We summed the Consequences of Introduction and Likelihood of Introduction values to estimate overall Pest Risk Potentials, which describe risk in the absence of mitigation. -
Ground Beetle Assemblages on Illinois Algific Slopes: a Rare Habitat Threatened by Climate Change
Ground Beetle assemblages on Illinois algific slopes: a rare habitat threatened by climate change by: Steven J. Taylor, Ph.D. Alan D. Yanahan Illinois Natural History Survey Department of Entomology University of Illinois at Urbana-Champaign 320 Morrill Hall 1816 South Oak Street University of Illinois at Urbana-Champaign Champaign, IL 61820 505 S. Goodwin Ave [email protected] Urbana, IL 61801 report submitted to: Illinois Department of Natural Resources Office of Resource Conservation, Federal Aid / Special Funds Section One Natural Resources Way Springfield, Illinois 62702-1271 Fund Title: 375 IDNR 12-016W I INHS Technical Report 2013 (01) 5 January 2013 Prairie Research Institute, University of Illinois at Urbana Champaign William Shilts, Executive Director Illinois Natural History Survey Brian D. Anderson, Director 1816 South Oak Street Champaign, IL 61820 217-333-6830 Ground Beetle assemblages on Illinois algific slopes: a rare habitat threatened by climate change Steven J. Taylor & Alan D. Yanahan University of Illinois at Urbana-Champaign During the Pleistocene, glacial advances left a small gap in the northwestern corner of Illinois, southwestern Wisconsin, and northeastern Iowa, which were never covered by the advancing Pleistocene glaciers (Taylor et al. 2009, p. 8, fig. 2.2). This is the Driftless Area – and it is one of Illinois’ most unique natural regions, comprising little more than 1% of the state. Illinois’ Driftless Area harbors more than 30 threatened or endangered plant species, and several unique habitat types. Among these habitats are talus, or scree, slopes, some of which retain ice throughout the year. The talus slopes that retain ice through the summer, and thus form a habitat which rarely exceeds 50 °F, even when the surrounding air temperature is in the 90’s °F, are known as “algific slopes.” While there are numerous examples of algific slopes in Iowa and Wisconsin, this habitat is very rare in Illinois (fewer than ten truly algific sites are known in the state). -
The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al. -
The Evolution and Genomic Basis of Beetle Diversity
The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State -
Phasmida (Stick and Leaf Insects)
● Phasmida (Stick and leaf insects) Class Insecta Order Phasmida Number of families 8 Photo: A leaf insect (Phyllium bioculatum) in Japan. (Photo by ©Ron Austing/Photo Researchers, Inc. Reproduced by permission.) Evolution and systematics Anareolatae. The Timematodea has only one family, the The oldest fossil specimens of Phasmida date to the Tri- Timematidae (1 genus, 21 species). These small stick insects assic period—as long ago as 225 million years. Relatively few are not typical phasmids, having the ability to jump, unlike fossil species have been found, and they include doubtful almost all other species in the order. It is questionable whether records. Occasionally a puzzle to entomologists, the Phasmida they are indeed phasmids, and phylogenetic research is not (whose name derives from a Greek word meaning “appari- conclusive. Studies relating to phylogeny are scarce and lim- tion”) comprise stick and leaf insects, generally accepted as ited in scope. The eggs of each phasmid are distinctive and orthopteroid insects. Other alternatives have been proposed, are important in classification of these insects. however. There are about 3,000 species of phasmids, although in this understudied order this number probably includes about 30% as yet unidentified synonyms (repeated descrip- Physical characteristics tions). Numerous species still await formal description. Stick insects range in length from Timema cristinae at 0.46 in (11.6 mm) to Phobaeticus kirbyi at 12.9 in (328 mm), or 21.5 Extant species usually are divided into eight families, in (546 mm) with legs outstretched. Numerous phasmid “gi- though some researchers cite just two, based on a reluctance ants” easily rank as the world’s longest insects. -
From Guatemala
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 2019 A contribution to the knowledge of Dermestidae (Coleoptera) from Guatemala José Francisco García Ochaeta Jiří Háva Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons 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. December 23 2019 INSECTA 5 ######## A Journal of World Insect Systematics MUNDI 0743 A contribution to the knowledge of Dermestidae (Coleoptera) from Guatemala José Francisco García-Ochaeta Laboratorio de Diagnóstico Fitosanitario Ministerio de Agricultura Ganadería y Alimentación Petén, Guatemala Jiří Háva Daugavpils University, Institute of Life Sciences and Technology, Department of Biosystematics, Vienības Str. 13 Daugavpils, LV - 5401, Latvia Date of issue: December 23, 2019 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL José Francisco García-Ochaeta and Jiří Háva A contribution to the knowledge of Dermestidae (Coleoptera) from Guatemala Insecta Mundi 0743: 1–5 ZooBank Registered: urn:lsid:zoobank.org:pub:10DBA1DD-B82C-4001-80CD-B16AAF9C98CA Published in 2019 by Center for Systematic Entomology, Inc. P.O. Box 141874 Gainesville, FL 32614-1874 USA http://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. -
Lake Rotokare Scenic Reserve Invertebrate Ecological Restoration Proposal
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Lincoln University Research Archive Bio-Protection & Ecology Division Lake Rotokare Scenic Reserve Invertebrate Ecological Restoration Proposal Mike Bowie Lincoln University Wildlife Management Report No. 47 ISSN: 1177‐6242 ISBN: 978‐0‐86476‐222‐1 Lincoln University Wildlife Management Report No. 47 Lake Rotokare Scenic Reserve Invertebrate Ecological Restoration Proposal Mike Bowie Bio‐Protection and Ecology Division P.O. Box 84 Lincoln University [email protected] Prepared for: Lake Rotokare Scenic Reserve Trust October 2008 Lake Rotokare Scenic Reserve Invertebrate Ecological Restoration Proposal 1. Introduction Rotokare Scenic Reserve is situated 12 km east of Eltham, South Taranaki, and is a popular recreation area for boating, walking and enjoying the scenery. The reserve consists of 230 ha of forested hill country, including a 17.8 ha lake and extensive wetland. Lake Rotokare is within the tribal area of the Ngati Ruanui and Ngati Tupaea people who used the area to collect food. Mature forested areas provide habitat for many birds including the fern bird (Sphenoeacus fulvus) and spotless crake (Porzana tabuensis), while the banded kokopu (Galaxias fasciatus) and eels (Anguilla australis schmidtii and Anguilla dieffenbachii) are found in streams and the lake, and the gold‐striped gecko (Hoplodactylus chrysosireticus) in the flax margins. In 2004 a broad group of users of the reserve established the Lake Rotokare Scenic Reserve Trust with the following mission statements: “To achieve the highest possible standard of pest control/eradication with or without a pest‐proof fence and to achieve a mainland island” “To have due regard for recreational users of Lake Rotokare Scenic Reserve” The Trust has raised funds and erected a predator exclusion fence around the 8.4 km reserve perimeter. -
Phasmid Studies ISSN 0966-0011 Volume 9, Numbers 1 & 2
Phasmid Studies ISSN 0966-0011 volume 9, numbers 1 & 2. Contents Species Report PSG. 122, Anisomorpha monstrosa Hebard Paul A. Hoskisson . 1 Cigarrophasma, a new genus of stick-insect (Phasmatidae) from Australia Paul D. Brock & Jack Hasenpusch . 0 •••••• 0 ••• 0 ••••••• 4 A review of the genus Medaura Stal, 1875 (Phasmatidae: Phasmatinae), including the description of a new species from Bangladesh Paul Do Brock & Nicolas Cliquennois 11 First records and discovery of two new species of Anisomorpha Gray (Phasmida: Pseudophasmatidae) in Haiti and Dominican Republic Daniel E. Perez-Gelabert 0 .. .. 0 • • • • • • 0 • • • • 0 • • 0 • 0 • • 0 0 • • • 27 Species report on Pharnacia biceps Redtenbacher, PSG 203 Wim Potvin 0 ••• 28 How Anisomorpha got its stripes? Paul Hoskisson . 33 Reviews and Abstracts Book Reviews . 35 Phasmid Abstracts 38 Cover illustr ation : Orthonecroscia pulcherrima Kirby, drawing by PoE. Bragg. Species Report PSG. 122, Anisomorpha monstrosa Hebard Paul A. Hoskisson, School of Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool, 13 3AF, UK. With illustrations by P.E. Bragg. Abstract This report summarises the care and breeding of Anisomorpha monstrosa Hebard, the largest species in the genus. Behaviour and defence mechanism are also discussed along with descriptions of the eggs, nymphs, and adults. Key words Phasmida, Anisomorpha monstrosa, Pseudophasmatinae, Rearing, Distribution, Defence. Taxonomy Anisomorpha monstrosa belongs to the sub-family Pseudophasmatinae. It was described in 1932 by Hebard (1932: 214) and is the largest species in the genus. The type specimen is a female collected from Merida, in Yucatan, Mexico. Culture History The original culture of this species was collected in Belize, approximately 150km north of Belize City by Jan Meerman in 1993 or 1994 (D'Hulster, personal communication). -
Temporal Lags and Overlap in the Diversification of Weevils and Flowering Plants
Temporal lags and overlap in the diversification of weevils and flowering plants Duane D. McKennaa,1, Andrea S. Sequeirab, Adriana E. Marvaldic, and Brian D. Farrella aDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138; bDepartment of Biological Sciences, Wellesley College, Wellesley, MA 02481; and cInstituto Argentino de Investigaciones de Zonas Aridas, Consejo Nacional de Investigaciones Científicas y Te´cnicas, C.C. 507, 5500 Mendoza, Argentina Edited by May R. Berenbaum, University of Illinois at Urbana-Champaign, Urbana, IL, and approved March 3, 2009 (received for review October 22, 2008) The extraordinary diversity of herbivorous beetles is usually at- tributed to coevolution with angiosperms. However, the degree and nature of contemporaneity in beetle and angiosperm diversi- fication remain unclear. Here we present a large-scale molecular phylogeny for weevils (herbivorous beetles in the superfamily Curculionoidea), one of the most diverse lineages of insects, based on Ϸ8 kilobases of DNA sequence data from a worldwide sample including all families and subfamilies. Estimated divergence times derived from the combined molecular and fossil data indicate diversification into most families occurred on gymnosperms in the Jurassic, beginning Ϸ166 Ma. Subsequent colonization of early crown-group angiosperms occurred during the Early Cretaceous, but this alone evidently did not lead to an immediate and ma- jor diversification event in weevils. Comparative trends in weevil diversification and angiosperm dominance reveal that massive EVOLUTION diversification began in the mid-Cretaceous (ca. 112.0 to 93.5 Ma), when angiosperms first rose to widespread floristic dominance. These and other evidence suggest a deep and complex history of coevolution between weevils and angiosperms, including codiver- sification, resource tracking, and sequential evolution.