What Do Insects Do for a Living? Common Habits Predators
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Beetle Appreciation Diversity and Classification of Common Beetle Families Christopher E
Beetle Appreciation Diversity and Classification of Common Beetle Families Christopher E. Carlton Louisiana State Arthropod Museum Coleoptera Families Everyone Should Know (Checklist) Suborder Adephaga Suborder Polyphaga, cont. •Carabidae Superfamily Scarabaeoidea •Dytiscidae •Lucanidae •Gyrinidae •Passalidae Suborder Polyphaga •Scarabaeidae Superfamily Staphylinoidea Superfamily Buprestoidea •Ptiliidae •Buprestidae •Silphidae Superfamily Byrroidea •Staphylinidae •Heteroceridae Superfamily Hydrophiloidea •Dryopidae •Hydrophilidae •Elmidae •Histeridae Superfamily Elateroidea •Elateridae Coleoptera Families Everyone Should Know (Checklist, cont.) Suborder Polyphaga, cont. Suborder Polyphaga, cont. Superfamily Cantharoidea Superfamily Cucujoidea •Lycidae •Nitidulidae •Cantharidae •Silvanidae •Lampyridae •Cucujidae Superfamily Bostrichoidea •Erotylidae •Dermestidae •Coccinellidae Bostrichidae Superfamily Tenebrionoidea •Anobiidae •Tenebrionidae Superfamily Cleroidea •Mordellidae •Cleridae •Meloidae •Anthicidae Coleoptera Families Everyone Should Know (Checklist, cont.) Suborder Polyphaga, cont. Superfamily Chrysomeloidea •Chrysomelidae •Cerambycidae Superfamily Curculionoidea •Brentidae •Curculionidae Total: 35 families of 131 in the U.S. Suborder Adephaga Family Carabidae “Ground and Tiger Beetles” Terrestrial predators or herbivores (few). 2600 N. A. spp. Suborder Adephaga Family Dytiscidae “Predacious diving beetles” Adults and larvae aquatic predators. 500 N. A. spp. Suborder Adephaga Family Gyrindae “Whirligig beetles” Aquatic, on water -
Coleoptera Identifying the Beetles
6/17/2020 Coleoptera Identifying the Beetles Who we are: Matt Hamblin [email protected] Graduate of Kansas State University in Manhattan, KS. Bachelors of Science in Fisheries, Wildlife and Conservation Biology Minor in Entomology Began M.S. in Entomology Fall 2018 focusing on Entomology Education Who we are: Jacqueline Maille [email protected] Graduate of Kansas State University in Manhattan, KS with M.S. in Entomology. Austin Peay State University in Clarksville, TN with a Bachelors of Science in Biology, Minor Chemistry Began Ph.D. iin Entomology with KSU and USDA-SPIERU in Spring 2020 Focusing on Stored Product Pest Sensory Systems and Management 1 6/17/2020 Who we are: Isaac Fox [email protected] 2016 Kansas 4-H Entomology Award Winner Pest Scout at Arnold’s Greenhouse Distribution, Abundance and Diversity Global distribution Beetles account for ~25% of all life forms ~390,000 species worldwide What distinguishes a beetle? 1. Hard forewings called elytra 2. Mandibles move horizontally 3. Antennae with usually 11 or less segments exceptions (Cerambycidae Rhipiceridae) 4. Holometabolous 2 6/17/2020 Anatomy Taxonomically Important Features Amount of tarsi Tarsal spurs/ spines Antennae placement and features Elytra features Eyes Body Form Antennae Forms Filiform = thread-like Moniliform = beaded Serrate = sawtoothed Setaceous = bristle-like Lamellate = nested plates Pectinate = comb-like Plumose = long hairs Clavate = gradually clubbed Capitate = abruptly clubbed Aristate = pouch-like with one lateral bristle Nicrophilus americanus Silphidae, American Burying Beetle Counties with protected critical habitats: Montgomery, Elk, Chautauqua, and Wilson Red-tipped antennae, red pronotum The ecological services section, Kansas department of Wildlife, Parks, and Tourism 3 6/17/2020 Suborders Adephaga vs Polyphaga Families ~176 described families in the U.S. -
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 -
A Thesis Entitled Influence of Soil-Quality on Coffee-Plant Quality
A Thesis entitled Influence of Soil-Quality on Coffee-Plant Quality and a Complex Tropical Insect Food Web by David J. Gonthier Submitted to the Graduate Faculty as partial fulfillment of the requirements for the Master of Science in Biology (Ecology track) Dr. Stacy Philpott, Committee Chair Dr. Scott Heckathorn, Committee Member Dr. Ivette Perfecto, Committee Member Dr. Patricia Komuniecki, Dean College of Graduate Studies The University of Toledo May 2010 Copyright 2010, David J. Gonthier This document is copyrighted material. Under copyright law, no parts of this document may be reproduced without the expressed permission of the author. An Abstract of Influence of Soil-Quality on Coffee-Plant Quality and a Complex Tropical Insect Food Web by David J. Gonthier Submitted to the Graduate Faculty as partial fulfillment of the requirements for the Master of Science in Biology (Ecology track) The University of Toledo May 2010 Tropical systems are complex, species diverse, and are often regulated by top-down forces (higher trophic levels control lower trophic levels). In many ecosystems insects, especially herbivores and their mutualists, may be strongly affected by plant quality and other bottom-up controls (nutrient availability, plant genetic variation, ect.). Yet few have asked how plant quality (nutritional and defensive plant traits) can contribute to the population regulation and the complexity of these systems. In this thesis, I investigate the importance of soil-quality to both the elemental and secondary metabolite content in coffee and ask how changes to plant quality can influence hemipteran herbivores, their ant-mutualists, predators, and insect communities in a tropical coffee agroecosystem. -
CPY Document Title
OIKOS 62: 363-369. Copenhagen 1991 Cost and evolution of a facultative mutualism between ants and lycaenid larvae (Lepidoptera) Robert K. Robbins Robbins, R.K. 1991. Cost and evolution of a facultative mutualism between ants and lycaenid larvae (Lepidoptera). - Oikos 62: 363-369. Larvae of Arawacus lincoides (Lycaenidae) reared in the lab with ants took 0.68 d longer to complete development than larvae without ants. Pupal weight was inde- pendent of whether a larva had been ant-tended. A 0.68 d delay in reaching age of first reproduction represents an estimated 1.0%-2.2% lowered intrinsic rate of increase for this continuously brooded species. I show that mutualism will be favored when the ratio of larval survival with ants to that without ants is greater than exp (dr), where d is the additional larval development time caused by feeding ants and r is the intrinsic rate of increase. Other things being equal, species with higher intrinsic rates of increase will be less likely to be mutualistic than their relatives with lower rates of increase. R. K. Robbins, Entomology, NHB Stop 127, Smithsonian Inst., Washington, DC 20560, USA. Butterfly larvae in the families Lycaenidae and Riodini- difficulties are partially overcome by examining facul- dae may interact mutualistically with ants (Pierce and tative mutualisms in which larvae in nature are some- Young 1986, Friedler and Maschwitz 1989a, Thomas et times tended and sometimes not tended by ants. al. 1989, DeVries 1990a). The benefit for ants is that Facultative larva-ant mutualisms vary among eu- they may obtain a significant portion of their energy maeine hairstreak butterflies (Lycaenidae: Theclinae: budget by eating larval secretions (Fiedler and Masch- Eumaeini) (DeVries 1990a). -
The Consequences of a Management Strategy for the Endangered Karner Blue Butterfly
THE CONSEQUENCES OF A MANAGEMENT STRATEGY FOR THE ENDANGERED KARNER BLUE BUTTERFLY Bradley A. Pickens A Thesis Submitted to the Graduate College of Bowling Green State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August 2006 Committee: Karen V. Root, Advisor Helen J. Michaels Juan L. Bouzat © 2006 Bradley A. Pickens All Rights Reserved iii ABSTRACT Karen V. Root, Advisor The effects of management on threatened and endangered species are difficult to discern, and yet, are vitally important for implementing adaptive management. The federally endangered Karner blue butterfly (Karner blue), Lycaeides melissa samuelis inhabits oak savanna or pine barrens, is a specialist on its host-plant, wild blue lupine, Lupinus perennis, and has two broods per year. The Karner blue was reintroduced into the globally rare black oak/lupine savannas of Ohio, USA in 1998. Current management practices involve burning 1/3, mowing 1/3, and leaving 1/3 of the lupine stems unmanaged at each site. Prescribed burning generally kills any Karner blue eggs present, so a trade-off exists between burning to maintain the habitat and Karner blue mortality. The objective of my research was to quantify the effects of this management strategy on the Karner blue. In the first part of my study, I examined several environmental factors, which influenced the nutritional quality (nitrogen and water content) of lupine to the Karner blue. My results showed management did not affect lupine nutrition for either brood. For the second brood, I found that vegetation density best predicted lupine nutritional quality, but canopy cover and aspect had an impact as well. -
American Burying Beetle
American Burying Beetle U.S. Fish & Wildlife Service 9014 East 21st Street Tulsa, Oklahoma 74129 Nicrophorus americanus - Olivier 918- 5 8 1 - 7458 6 / 4 / 2 0 1 4 Available online http://www.fws.gov/southwest/es/Oklahoma/ABB_Add_Info.htm American Burying Beetle (ABB) Nicrophorus americanus Executive Summary The American burying beetle (Nicrophorus americanus, ABB) is the largest silphid (carrion beetle) in North America, reaching 1.0 to 1.8 inches (2.5-4.5 cm) in length (Wilson 1971, Anderson 1982, Backlund and Marrone 1997). The most diagnostic feature of the ABB is the large orange-red marking on the raised portion of the pronotum (hard back plate of the front portion of the thorax of insects), a feature shared with no other members of the genus in North America (USFWS 1991). The ABB is a nocturnal species that lives only for one year. The beetles are active in the summer months and bury themselves in the soil for the duration of the winter. Immature beetles (tenerals) emerge in late summer, over-winter as adults, and comprise the breeding population the following summer (Kozol 1990a). Adults and larvae are dependent on carrion (animal carcass) for food and reproduction. They must compete for carrion with other invertebrate and vertebrate species. Having wings, ABBs are strong fliers and have been reported moving distances ranging from 0.10 to 18.14 miles (0-29.19 kilometers) in various parts of their range (Bedick et al. 1999, Creighton and Schnell 1998, Jurzenski 2012, Jurzenski et al. 2011, Schnell et al. 1997-2006). In Oklahoma, ABBs have been recorded to move up to 10 km (6.2 miles) in 6 nights (Creighton and Schnell 1998). -
Karner Blue Butterfly
Environmental Entomology Advance Access published April 22, 2016 Environmental Entomology, 2016, 1–9 doi: 10.1093/ee/nvw036 Plant–Insect Interactions Research Article The Relationship Between Ants and Lycaeides melissa samuelis (Lepidoptera: Lycaenidae) at Concord Pine Barrens, NH, USA Elizabeth G. Pascale1 and Rachel K. Thiet Department of Environmental Studies, Antioch University New England, 40 Avon St., Keene, NH 03431 ([email protected]; [email protected]) and 1Corresponding author, e-mail: [email protected] Received 5 December 2015; Accepted 20 April 2016 Abstract Downloaded from The Karner blue butterfly (Lycaeides melissa samuelis Nabokov) (Lepidoptera: Lycaenidae) is a federally listed, endangered species that has experienced dramatic decline over its historic range. In surviving populations, Karner blue butterflies have a facultative mutualism with ants that could be critically important to their survival where their populations are threatened by habitat loss or disturbance. In this study, we investigated the effects of ants, wild blue lupine population status (native or restored), and fire on adult Karner blue butterfly abundance http://ee.oxfordjournals.org/ at the Concord Pine Barrens, NH, USA. Ant frequency (the number of times we collected each ant species in our pitfall traps) was higher in restored than native lupine treatments regardless of burn status during both Karner blue butterfly broods, and the trend was statistically significant during the second brood. We observed a posi- tive relationship between adult Karner blue butterfly abundance and ant frequency during the first brood, partic- ularly on native lupine, regardless of burn treatment. During the second brood, adult Karner blue butterfly abun- dance and ant frequency were not significantly correlated in any treatments or their combinations. -
Lycaenidae): Phylogeny, Ecology, and Conservation John Mathew Old Dominion University
Old Dominion University ODU Digital Commons Biological Sciences Theses & Dissertations Biological Sciences Summer 2003 Aphytophagy in the Miletinae (Lycaenidae): Phylogeny, Ecology, and Conservation John Mathew Old Dominion University Follow this and additional works at: https://digitalcommons.odu.edu/biology_etds Part of the Ecology and Evolutionary Biology Commons, Entomology Commons, and the Genetics Commons Recommended Citation Mathew, John. "Aphytophagy in the Miletinae (Lycaenidae): Phylogeny, Ecology, and Conservation" (2003). Doctor of Philosophy (PhD), dissertation, Biological Sciences, Old Dominion University, DOI: 10.25777/v7rh-mb21 https://digitalcommons.odu.edu/biology_etds/74 This Dissertation is brought to you for free and open access by the Biological Sciences at ODU Digital Commons. It has been accepted for inclusion in Biological Sciences Theses & Dissertations by an authorized administrator of ODU Digital Commons. For more information, please contact [email protected]. APHYTOPHAGY IN THE MILETINAE (LYCAENIDAE): PHYLOGENY, ECOLOGY, AND CONSERVATION by John Mathew B.Sc. June 1990, Madras Christian College M.Sc. June 1992, Madras Christian College M.Phil. May 1994, Madras University A Dissertation Submitted to the Faculty of Old Dominion University in Partial Fulfillment of the Requirement for the Degree of DOCTOR OF PHILOSOPHY ECOLOGICAL SCIENCES OLD DOMINION UNIVERSITY August 2003 Approved by: Deborah A. Waller (Co-Director) »mi E. Pierce (Co-Director) H. Savitzky (Member) Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. ABSTRACT APHYTOPHAGY IN THE MILETINAE (LYCAENIDAE): PHYTOGENY, ECOLOGY AND CONSERVATION John Mathew Old Dominion University, 2003 Co-Directors of Advisory Committee: Dr. Deborah A. Waller Dr. Naomi E. Pierce Less than 1% of all Lepidoptera are aphytophagous; of these, a considerable proportion is found in the family Lycaenidae. -
Do Ants Enhance Diversification in Lycaenid Butterflies? Phylogeographic Evidence from a Model Myrmecophile, Jalmenus Evagoras
Evolution, 60(2), 2006, pp. 315±327 DO ANTS ENHANCE DIVERSIFICATION IN LYCAENID BUTTERFLIES? PHYLOGEOGRAPHIC EVIDENCE FROM A MODEL MYRMECOPHILE, JALMENUS EVAGORAS ROD EASTWOOD,1,2 NAOMI E. PIERCE,3,4 R. L. KITCHING,1,5 AND JANE M. HUGHES1,6 1Australian School of Environmental Studies, Grif®th University, Nathan 4111, Queensland, Australia 2E-mail: r.eastwood@grif®th.edu.au 3Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, Massachusetts 02138 4E-mail: [email protected] 5E-mail: r.kitching@grif®th.edu.au 6E-mail: jane.hughes@grif®th.edu.au Abstract. The ant-tended Australian butter¯y, Jalmenus evagoras, has been a model system for studying the ecology and evolution of mutualism. A phylogeographic analysis of mitochondrial DNA cytochrome oxidase I sequences from 242 butter¯ies (615 bp) and 66 attendant ants (585 bp) from 22 populations was carried out to explore the relationship between ant association and butter¯y population structure. This analysis revealed 12 closely related butter¯y haplotypes in three distinct clades roughly corresponding to three allopatric subpopulations of the butter¯ies. Minimal genetic diversity and widespread haplotypes within biogeographical regions suggest high levels of matrilineal gene ¯ow. Attendant ants are signi®cantly more diverse than was previously thought, with at least seven well-de®ned clades corresponding to independent morphological determinations, distributed throughout the range of the butter¯ies. Nested analysis of molecular variance showed that biogeography, host plant, and ant associate all contribute signi®cantly in explaining variation in butter¯y genetic diversity, but these variables are not independent of one another. -
The Fluctuating Asymmetry of the Butterfly Wing Pattern Does Not Change Along an Industrial Pollution Gradient
S S symmetry Article The Fluctuating Asymmetry of the Butterfly Wing Pattern Does Not Change along an Industrial Pollution Gradient Vitali Zverev and Mikhail V. Kozlov * Department of Biology, University of Turku, 20014 Turku, Finland; vitzve@utu.fi * Correspondence: mikoz@utu.fi Abstract: The rapid and selective responses to changes in habitat structure and climate have made butterflies valuable environmental indicators. In this study, we asked whether the decline in butterfly populations near the copper-nickel smelter in Monchegorsk in northwestern Russia is accompanied by phenotypic stress responses to toxic pollutants, expressed as a decrease in body size and an increase in fluctuating asymmetry. We measured the concentrations of nickel and copper, forewing length, and fluctuating asymmetry in two elements of wing patterns in Boloria euphrosyne, Plebejus idas, and Agriades optilete collected 1–65 km from Monchegorsk. Body metal concentrations increased toward the smelter, confirming the local origin of the collected butterflies. The wings of butterflies from the most polluted sites were 5–8% shorter than those in unpolluted localities, suggesting adverse effects of pollution on butterfly fitness due to larval feeding on contaminated plants. However, fluctuating asymmetry averaged across two hindwing spots did not change systematically with pollution, thereby questioning the use of fluctuating asymmetry as an indicator of habitat quality in butterfly conservation projects. Keywords: copper-nickel smelter; fluctuating asymmetry; Kola Peninsula; Lepidoptera; phenotypic Citation: Zverev, V.; Kozlov, M.V. stress responses; wing length The Fluctuating Asymmetry of the Butterfly Wing Pattern Does Not Change along an Industrial Pollution Gradient. Symmetry 2021, 13, 626. https://doi.org/10.3390/sym13040626 1. -
A New Subspec Ies of Jalmenus Inous H Ewi T So N
Australian Entomologist. 2007, 34 (3): 77-83 77 ANEW SUBSPEC IES OF JALMENUS INO US HEWI TSO N (LE PIDOPTERA: LYCAENIDAE) FROM SHA RK BAY, WESTERN AUSTRA LIA STEPHEN J. JOHNSON' and PETER S. VALENTINE' IQueensland Museum , PO Box 3300, South Bank, QId 4101 lEarth and Environmental Sciences, James Cook University. Townsville. Qld 481I Abstract Jal menus inous bronwynae subsp. n. is described for the first record of the genus Jalmenus Hubner from the Shark Bay area in Western Australia. The new subspecies is the smallest in the genus and is isolated by more than 700 km from the nearest populations of related taxa. It is recorded breeding on Acacia ligulata A. Cunn ex Benth, a species not previously known as a host plant for Jalmenus. Immature stages are attended by two species of ants within the Iridomyrmex rufoniger group. Introduc tion There appear to be no recent records of Jalmenus Hubner from the Shark Bay area in Western Australia, despite some collection effort in the area during the last 20 years. The record ofJalmenus inous Hewitson, from further north at Carnarvon (Waterhouse and Lyell 1914), is presumably the basis for the distribution map in Common and Waterhouse (198 1). This record was doubted by Braby (2000), whose map shows J. inous restricted to the far southwest and including the distribution of J. i. notocrucifer Johnson, Hay & Bollam. Both Common and Waterhouse (198 1) and Braby (2000) showed the distribution of Jalmenus icilius Hewitson as covering a large part of southwestern Australia. Another species, J. clementi Druce, occurs 150 km further north in the Northwest Cape region.