Evolution of Ant-Mimicking Beetles Edcator Materials
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Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Papers in Entomology Museum, University of Nebraska State 12-2009 Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii Mary Liz Jameson Wichita State University, [email protected] Darcy E. Oishi 2Hawaii Department of Agriculture, Plant Pest Control Branch, Honolulu, [email protected] Brett C. Ratcliffe University of Nebraska-Lincoln, [email protected] Grant T. McQuate USDA-ARS-PBARC, U.S. Pacific Basin Agricultural Research Center, Hilo, HI, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/entomologypapers Part of the Entomology Commons Jameson, Mary Liz; Oishi, Darcy E.; Ratcliffe, Brett C.; and McQuate, Grant T., "Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii" (2009). Papers in Entomology. 147. https://digitalcommons.unl.edu/entomologypapers/147 This Article is brought to you for free and open access by the Museum, University of Nebraska State at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Papers in Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. AProcddition. HawaiianAl inv AEsiventomol scA.r SAocbs. in(2009) HAwA 41:25–30ii 25 Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii Mary Liz Jameson1, Darcy E. Oishi2, Brett C. Ratcliffe3, and Grant T. McQuate4 1Wichita State University, Department of Biological Sciences, 537 Hubbard Hall, Wichita, Kansas 67260 [email protected]; 2Hawaii Department of Agriculture, Plant Pest Control Branch, 1428 South King St., Honolulu, HI 96814 [email protected]; 3University of Nebraska State Museum, Systematics Research Collections, W436 Nebraska Hall, University of Nebraska, Lincoln, Nebraska 68588 [email protected]; 4USDA-ARS-PBARC, U.S. -
Ant Trails: a Key to Management with Baits1
ENY-259 Ant Trails: A Key to Management with Baits1 John Klotz, Dave Williams, Byron Reid, Karen Vail, and Phil Koehler2 Communication in the ants is based on chemical straight back to the nest (Figure 1). Somehow on the signals. These chemicals are called pheromones and outgoing trip she can keep track of her position with vary from alarm and nestmate recognition, to the one respect to her nest, and, on the return trip, uses this we will focus on here, recruitment. All of the pest information to take the shorter, more direct route ants use odor trails for orientation, but these trails home. On the way back to the nest, she lays down an differ from one species to another. Where the odor trail. Once back in the nest, this scout ant then pheromones originate in the ant's body, their alerts her nestmates of the food find, which chemical composition, as well as how long they last, encourages them to leave the nest. These recruited all vary from one ant species to the next. In fire ants, ants will follow the odor trail directly to the food the trail chemical is produced by the Dufour's gland, source. In turn, each ant will reinforce the odor trail which is named after its discoverer, Dufour, and is until the food is gone. This behavior is a highly laid down by the stinger. This pheromone is made up efficient means of exploiting a temporary food of molecules which evaporate very quickly. Thus, the resource. fire ant's odor trail is very short-lived. -
Alien Dominance of the Parasitoid Wasp Community Along an Elevation Gradient on Hawai’I Island
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln USGS Staff -- Published Research US Geological Survey 2008 Alien dominance of the parasitoid wasp community along an elevation gradient on Hawai’i Island Robert W. Peck U.S. Geological Survey, [email protected] Paul C. Banko U.S. Geological Survey Marla Schwarzfeld U.S. Geological Survey Melody Euaparadorn U.S. Geological Survey Kevin W. Brinck U.S. Geological Survey Follow this and additional works at: https://digitalcommons.unl.edu/usgsstaffpub Peck, Robert W.; Banko, Paul C.; Schwarzfeld, Marla; Euaparadorn, Melody; and Brinck, Kevin W., "Alien dominance of the parasitoid wasp community along an elevation gradient on Hawai’i Island" (2008). USGS Staff -- Published Research. 652. https://digitalcommons.unl.edu/usgsstaffpub/652 This Article is brought to you for free and open access by the US Geological Survey at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in USGS Staff -- Published Research by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Biol Invasions (2008) 10:1441–1455 DOI 10.1007/s10530-008-9218-1 ORIGINAL PAPER Alien dominance of the parasitoid wasp community along an elevation gradient on Hawai’i Island Robert W. Peck Æ Paul C. Banko Æ Marla Schwarzfeld Æ Melody Euaparadorn Æ Kevin W. Brinck Received: 7 December 2007 / Accepted: 21 January 2008 / Published online: 6 February 2008 Ó Springer Science+Business Media B.V. 2008 Abstract Through intentional and accidental increased with increasing elevation, with all three introduction, more than 100 species of alien Ichneu- elevations differing significantly from each other. monidae and Braconidae (Hymenoptera) have Nine species purposely introduced to control pest become established in the Hawaiian Islands. -
Mountain Pine Beetle Voltinism and Life History Characteristics Across Latitudinal and Elevational Gradients in the Western United States
For. Sci. 60(3):434–449 FUNDAMENTAL RESEARCH http://dx.doi.org/10.5849/forsci.13-056 entomology & pathology Mountain Pine Beetle Voltinism and Life History Characteristics across Latitudinal and Elevational Gradients in the Western United States Barbara Bentz, James Vandygriff, Camille Jensen, Tom Coleman, Patricia Maloney, Sheri Smith, Amanda Grady, and Greta Schen-Langenheim Substantial genetic variation in development time is known to exist among mountain pine beetle (Dendroctonus ponderosae Hopkins) populations across the western United States. The effect of this variation on geographic patterns in voltinism (generation time) and thermal requirements to produce specific voltinism pathways have not been investigated. The influence of voltinism on fitness traits, body size, and sex ratio is also unclear. We monitored mountain pine beetle voltinism, adult body size, sex ratio, and air temperatures at sites across latitudinal and elevational gradients in the western United States. With the exception of two sites at the coolest and warmest locations, the number of days required to complete a generation was similar. Thermal units required to achieve a generation, however, were significantly less for individuals at the coolest sites. Evolved adaptations explain this pattern, including developmental rates and thresholds that serve to synchronize cohorts and minimize cold-sensitive life stages in winter. These same adaptations reduce the capacity of mountain pine beetle at the warmest sites to take full advantage of increased thermal units, limiting the capacity for bivoltinism within the current realized distribution. Temperature was not correlated with adult size and sex ratio, and size was greatest in host trees other than lodgepole pine (Pinus contorta Dougl.). -
Rare Native Animals of RI
RARE NATIVE ANIMALS OF RHODE ISLAND Revised: March, 2006 ABOUT THIS LIST The list is divided by vertebrates and invertebrates and is arranged taxonomically according to the recognized authority cited before each group. Appropriate synonomy is included where names have changed since publication of the cited authority. The Natural Heritage Program's Rare Native Plants of Rhode Island includes an estimate of the number of "extant populations" for each listed plant species, a figure which has been helpful in assessing the health of each species. Because animals are mobile, some exhibiting annual long-distance migrations, it is not possible to derive a population index that can be applied to all animal groups. The status assigned to each species (see definitions below) provides some indication of its range, relative abundance, and vulnerability to decline. More specific and pertinent data is available from the Natural Heritage Program, the Rhode Island Endangered Species Program, and the Rhode Island Natural History Survey. STATUS. The status of each species is designated by letter codes as defined: (FE) Federally Endangered (7 species currently listed) (FT) Federally Threatened (2 species currently listed) (SE) State Endangered Native species in imminent danger of extirpation from Rhode Island. These taxa may meet one or more of the following criteria: 1. Formerly considered by the U.S. Fish and Wildlife Service for Federal listing as endangered or threatened. 2. Known from an estimated 1-2 total populations in the state. 3. Apparently globally rare or threatened; estimated at 100 or fewer populations range-wide. Animals listed as State Endangered are protected under the provisions of the Rhode Island State Endangered Species Act, Title 20 of the General Laws of the State of Rhode Island. -
Local and Landscape Effects on Carrion-Associated Rove Beetle (Coleoptera: Staphylinidae) Communities in German Forests
insects Article Local and Landscape Effects on Carrion-Associated Rove Beetle (Coleoptera: Staphylinidae) Communities in German Forests Sandra Weithmann 1,* , Jonas Kuppler 1 , Gregor Degasperi 2, Sandra Steiger 3 , Manfred Ayasse 1 and Christian von Hoermann 4 1 Institute of Evolutionary Ecology and Conservation Genomics, University of Ulm, 89069 Ulm, Germany; [email protected] (J.K.); [email protected] (M.A.) 2 Richard-Wagnerstraße 9, 6020 Innsbruck, Austria; [email protected] 3 Department of Evolutionary Animal Ecology, University of Bayreuth, 95447 Bayreuth, Germany; [email protected] 4 Department of Conservation and Research, Bavarian Forest National Park, 94481 Grafenau, Germany; [email protected] * Correspondence: [email protected] Received: 15 October 2020; Accepted: 21 November 2020; Published: 24 November 2020 Simple Summary: Increasing forest management practices by humans are threatening inherent insect biodiversity and thus important ecosystem services provided by them. One insect group which reacts sensitively to habitat changes are the rove beetles contributing to the maintenance of an undisturbed insect succession during decomposition by mainly hunting fly maggots. However, little is known about carrion-associated rove beetles due to poor taxonomic knowledge. In our study, we unveiled the human-induced and environmental drivers that modify rove beetle communities on vertebrate cadavers. At German forest sites selected by a gradient of management intensity, we contributed to the understanding of the rove beetle-mediated decomposition process. One main result is that an increasing human impact in forests changes rove beetle communities by promoting generalist and more open-habitat species coping with low structural heterogeneity, whereas species like Philonthus decorus get lost. -
List of Animal Species with Ranks October 2017
Washington Natural Heritage Program List of Animal Species with Ranks October 2017 The following list of animals known from Washington is complete for resident and transient vertebrates and several groups of invertebrates, including odonates, branchipods, tiger beetles, butterflies, gastropods, freshwater bivalves and bumble bees. Some species from other groups are included, especially where there are conservation concerns. Among these are the Palouse giant earthworm, a few moths and some of our mayflies and grasshoppers. Currently 857 vertebrate and 1,100 invertebrate taxa are included. Conservation status, in the form of range-wide, national and state ranks are assigned to each taxon. Information on species range and distribution, number of individuals, population trends and threats is collected into a ranking form, analyzed, and used to assign ranks. Ranks are updated periodically, as new information is collected. We welcome new information for any species on our list. Common Name Scientific Name Class Global Rank State Rank State Status Federal Status Northwestern Salamander Ambystoma gracile Amphibia G5 S5 Long-toed Salamander Ambystoma macrodactylum Amphibia G5 S5 Tiger Salamander Ambystoma tigrinum Amphibia G5 S3 Ensatina Ensatina eschscholtzii Amphibia G5 S5 Dunn's Salamander Plethodon dunni Amphibia G4 S3 C Larch Mountain Salamander Plethodon larselli Amphibia G3 S3 S Van Dyke's Salamander Plethodon vandykei Amphibia G3 S3 C Western Red-backed Salamander Plethodon vehiculum Amphibia G5 S5 Rough-skinned Newt Taricha granulosa -
Darkling Beetles and Mealworms Theresa A
Darkling Beetles and Mealworms Theresa A. Dellinger and Eric R. Day, Department of Entomology, Virginia Tech Description Darkling beetles belong in the beetle family Tenebrionidae, which consists of more than 20,000 species of beetles. Adult darkling beetles widely range in shape and size, with most measuring from 2 – 19 mm (0.13” – 0.75”). Adults are usually a reddish-brown to brownish-black in color and can be shiny or dull. The elytra (the wing covers) can be smooth, grooved, or otherwise sculptured. Most do not have colorful patterns on their wing covers. Adults are most active at night and tend to avoid bright lights. Darkling beetle larvae are often referred to as mealworms or false wireworms. They are long, hard-bodied grubs with a cylindrical shape and are shiny yellow-brown to darKer brown in color. They are active crawlers. Yellow mealworm larva, top. Dark mealworm larva, bottom. Clemson University-USDA Cooperative Adult yellow mealworm, Tenebrio molitor. Extension Slide Series, Bugwood.org. Clemson University-USDA Cooperative Extension Slide Series, Bugwood.org. Life Cycle Darkling beetles have a complete life cycle with egg, larval, pupal, and adult stages. Most species of darkling beetles have a slow rate of development and may live for a year as an adult. Species living on grains or other stored products may develop faster. Habitat/Distribution Darkling beetles are found throughout the world except for places with very cold climates. They are scavengers and omnivores, feeding on decomposing plant material, dead insects, fungi, and stored products. Only a handful of darkling beetles are considered pests; the vast majority of them live in the wild and pose no harm. -
Evolution Activity, Grade 11
Evolution Activity, Grade 11 Evolution Activities for Grade 11 Students at the Toronto Zoo 1 Evolution Activity, Grade 11 Table of Contents Pre-Zoo Activity 3-8 • Think, Pair, Share – Animals in Society and Role of Zoos 3-5 o Description 3 o Materials 3 o Four Corners Activity 6 o Background Information 7-8 Zoo Activity 9-19 • Teacher’s Notes 9-13 o General Information, Curriculum expectations, 9-10 materials, procedure o Evaluation Rubrics 11-12 o Glossary 13 • Student Assignment 14-19 o Part 1 – Mission Preparation at the Zoo 15-16 (Observation Sheets) o Part 2 – Scientific Notes 17 o Part 3 – Documentation: The Story 18 o Appendix – Animal signs 19 Evaluation 20 2 Evolution Activity, Grade 11 Suggested Pre-zoo activity Time needed : 35 minutes (or more) Type of activity : pair-share, small-group (approximately 2-3 students) Objective : encourage students to think about and evaluate the roles of animals in our society and the purposes of zoos along with their own attitudes or stands toward zoos Materials needed : a set of 8-16 statements and a mode of ranking (either above the line-below the line or diamond style ranking system) Special note : In order to manage time, teacher can chose to use any number of the statements as long as the 4 core statements listed bellow are included. Task : students work together to rank the statements about the treatment of animals. They should work together and try to negotiate a consensus, but if this is impossible they can either leave out the particular statement or write down a few lines in their notes as to why they would place them in a different category. -
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 -
Divergent Evolution in Antiherbivore Defences Within Species Complexes at a Single Amazonian Site
Journal of Ecology 2015, 103, 1107–1118 doi: 10.1111/1365-2745.12431 Divergent evolution in antiherbivore defences within species complexes at a single Amazonian site Marıa-Jose Endara1*, Alexander Weinhold1, James E. Cox2, Natasha L. Wiggins1, Phyllis D. Coley1,3 and Thomas A. Kursar1,3 1Department of Biology, The University of Utah, Salt Lake City, UT 84112-0840, USA; 2Health Sciences Center Core Research Facilities, School of Medicine, The University of Utah, Salt Lake City, UT 84112-0840, USA; and 3Smithsonian Tropical Research Institute, Balboa Box 0843-03092, Panama Summary 1. Classic theory in plant–insect interactions has linked herbivore pressure with diversification in plant species. We hypothesize that herbivores may exert divergent selection on defences, such that closely related plant species will be more different in defensive than in non-defensive traits. 2. We evaluated this hypothesis by investigating two clades of closely related plant species coexis- ting at a single site in the Peruvian Amazon: Inga capitata Desv. and Inga heterophylla Willd. spe- cies complexes. We compared how these lineages differ in the suite of chemical, biotic, phenological and developmental defences as compared to non-defensive traits that are related to habitat use and resource acquisition. We also collected insect herbivores feeding on the plants. 3. Our data show that sister lineages within both species complexes are more divergent in antiherbi- vore defences than in other non-defensive, functional traits. Moreover, the assemblages of herbivore communities are dissimilar between the populations of coexisting I. capitata lineages. 4. Synthesis. Our results are consistent with the idea that for the I. -
Altitudinal Variation of Dung Beetle (Scarabaeidae: Scarabaeinae
Global Ecology and Biogeography, (Global Ecol. Biogeogr.) (2005) 14, 327–337 Blackwell Publishing, Ltd. RESEARCH Altitudinal variation of dung beetle PAPER (Scarabaeidae: Scarabaeinae) assemblages in the Colombian Andes Federico Escobar1,2,*, Jorge M. Lobo3 and Gonzalo Halffter1 1Departamento de Biodiversidad y ABSTRACT Comportamiento Animal, Instituto de Ecología, Aim We describe the changes in species richness, rarity and composition with alti- A.C., Apartado Postal 63, 91000 Xalapa, tude, and explore whether the differences in Scarabaeinae dung beetle composition Veracruz, México; 2Programa de Inventarios de Biodiversidad, Instituto Humboldt, Apartado along five altitudinal transects of the same mountain range are related to altitude or Aéreo 8693 Santafé de Bogotá, Colombia; and if there are interregional differences in these altitudinal gradients. 3 Departamento de Biodiversidad y Biología Location Field work was carried out on the eastern slope of the eastern Cordillera, Evolutiva, Museo Nacional de Ciencias Colombian Andes, between Tamá Peak to the north, in the Tamá National Park Naturales (CSIC), c/José Gutiérrez Abascal, 2. (07°23′ N, 72°23′ W) and the San Miguel River (00°28′ N, 77°17′ W) to the south. E-28006 Madrid, Spain Methods Sampling was carried out between February 1997 and November 1999 in five regions spanning elevation gradients. In each gradient, six sites were chosen at 250 m intervals between 1000 and 2250 m a.s.l. Results We found a curvilinear relationship between altitude and mean species rich- ness, with a peak in richness at middle elevations. However, the diversity of dung beetle assemblages does not seem to be related to the interregional differences in environ- mental conditions.