Fall 2012 Bulletin of the Oregon Entomological Society
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STARR-DISSERTATION-2018.Pdf (6.554Mb)
The Effects of Land Use and Climate Change on Playa Wetlands and Their Invertebrate Communities. by Scott McKinley Starr, B.S., M.S. Dissertation In Biology Submitted to the Graduate Faculty of Texas Tech University in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Approved Dr. Nancy E. McIntyre Chair of Committee Dr. Llewellyn D. Densmore Dr. Kerry L. Griffis-Kyle Dr. Stephanie A. Lockwood Dr. Kevin R. Mulligan Dr. Mark A. Sheridan Dean of the Graduate School August, 2018 Copyright 2018, Scott Starr Texas Tech University, Scott Starr, August 2018 Acknowledgments The process of completing this dissertation has been a long road and many people and groups have helped me along the way. I first want to thank my dissertation advisor, Dr. Nancy McIntyre, for all her support and assistance through this degree. Without her guidance this process would have been unachievable. I also want to thank Dr. McIntyre for inviting me into her lab and for allowing me to be part of so many lab research projects that have helped to build my toolbox as a scientist. Second, I would like to thank my committee members Drs. Kerry Griffis-Kyle, Kevin Mulligan, Stephanie Lockwood, Lou Densmore, Richard Strauss, and Ximena Bernal for their guidance and suggestions that have helped to improve the research presented here. Third, I would like to thank my lab mates and undergraduate assistants: Steve Collins, Lucas Heintzman, Joe Drake, Ezra Auerbach, Devin Kilborn, Benjamin Breedlove, Shane Glidewell, Kimbree Knight, and Jennifer Long for their help in the field, lab, and for their support. -
Olive Clubtail (Stylurus Olivaceus) in Canada, Prepared Under Contract with Environment Canada
COSEWIC Assessment and Status Report on the Olive Clubtail Stylurus olivaceus in Canada ENDANGERED 2011 COSEWIC status reports are working documents used in assigning the status of wildlife species suspected of being at risk. This report may be cited as follows: COSEWIC. 2011. COSEWIC assessment and status report on the Olive Clubtail Stylurus olivaceus in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. x + 58 pp. (www.sararegistry.gc.ca/status/status_e.cfm). Production note: COSEWIC would like to acknowledge Robert A. Cannings, Sydney G. Cannings, Leah R. Ramsay and Richard J. Cannings for writing the status report on Olive Clubtail (Stylurus olivaceus) in Canada, prepared under contract with Environment Canada. This report was overseen and edited by Paul Catling, Co-chair of the COSEWIC Arthropods Specialist Subcommittee. For additional copies contact: COSEWIC Secretariat c/o Canadian Wildlife Service Environment Canada Ottawa, ON K1A 0H3 Tel.: 819-953-3215 Fax: 819-994-3684 E-mail: COSEWIC/[email protected] http://www.cosewic.gc.ca Également disponible en français sous le titre Ếvaluation et Rapport de situation du COSEPAC sur le gomphe olive (Stylurus olivaceus) au Canada. Cover illustration/photo: Olive Clubtail — Photo by Jim Johnson. Permission granted for reproduction. ©Her Majesty the Queen in Right of Canada, 2011. Catalogue No. CW69-14/637-2011E-PDF ISBN 978-1-100-18707-5 Recycled paper COSEWIC Assessment Summary Assessment Summary – May 2011 Common name Olive Clubtail Scientific name Stylurus olivaceus Status Endangered Reason for designation This highly rare, stream-dwelling dragonfly with striking blue eyes is known from only 5 locations within three separate regions of British Columbia. -
Dragonflies (Odonata) of the Northwest Territories Status Ranking And
DRAGONFLIES (ODONATA) OF THE NORTHWEST TERRITORIES STATUS RANKING AND PRELIMINARY ATLAS PAUL M. CATLING University of Ottawa 2003 TABLE OF CONTENTS Abstract ....................................................................3 Acknowledgements ...........................................................3 Methods ....................................................................3 The database .................................................................4 History .....................................................................5 Rejected taxa ................................................................5 Possible additions ............................................................5 Additional field inventory ......................................................7 Collection an Inventory of dragonflies .............................................8 Literature Cited .............................................................10 Appendix Table 1 - checklist ...................................................13 Appendix Table 2 - Atlas and ranking notes .......................................15 2 ABSTRACT: occurrences was provided by Dr. Rex Thirty-five species of Odonata are given Kenner, Dr. Donna Giberson, Dr. Nick status ranks in the Northwest Territories Donnelly and Dr. Robert Cannings (some based on number of occurrences and details provided below). General distributional area within the territory. Nine information on contacts and locations of species are ranked as S2, may be at risk, collections provided by Dr. Cannings -
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 -
Appendix A: Common and Scientific Names for Fish and Wildlife Species Found in Idaho
APPENDIX A: COMMON AND SCIENTIFIC NAMES FOR FISH AND WILDLIFE SPECIES FOUND IN IDAHO. How to Read the Lists. Within these lists, species are listed phylogenetically by class. In cases where phylogeny is incompletely understood, taxonomic units are arranged alphabetically. Listed below are definitions for interpreting NatureServe conservation status ranks (GRanks and SRanks). These ranks reflect an assessment of the condition of the species rangewide (GRank) and statewide (SRank). Rangewide ranks are assigned by NatureServe and statewide ranks are assigned by the Idaho Conservation Data Center. GX or SX Presumed extinct or extirpated: not located despite intensive searches and virtually no likelihood of rediscovery. GH or SH Possibly extinct or extirpated (historical): historically occurred, but may be rediscovered. Its presence may not have been verified in the past 20–40 years. A species could become SH without such a 20–40 year delay if the only known occurrences in the state were destroyed or if it had been extensively and unsuccessfully looked for. The SH rank is reserved for species for which some effort has been made to relocate occurrences, rather than simply using this status for all elements not known from verified extant occurrences. G1 or S1 Critically imperiled: at high risk because of extreme rarity (often 5 or fewer occurrences), rapidly declining numbers, or other factors that make it particularly vulnerable to rangewide extinction or extirpation. G2 or S2 Imperiled: at risk because of restricted range, few populations (often 20 or fewer), rapidly declining numbers, or other factors that make it vulnerable to rangewide extinction or extirpation. G3 or S3 Vulnerable: at moderate risk because of restricted range, relatively few populations (often 80 or fewer), recent and widespread declines, or other factors that make it vulnerable to rangewide extinction or extirpation. -
Ecography ECOG-02578 Pinkert, S., Brandl, R
Ecography ECOG-02578 Pinkert, S., Brandl, R. and Zeuss, D. 2016. Colour lightness of dragonfly assemblages across North America and Europe. – Ecography doi: 10.1111/ecog.02578 Supplementary material Appendix 1 Figures A1–A12, Table A1 and A2 1 Figure A1. Scatterplots between female and male colour lightness of 44 North American (Needham et al. 2000) and 19 European (Askew 1988) dragonfly species. Note that colour lightness of females and males is highly correlated. 2 Figure A2. Correlation of the average colour lightness of European dragonfly species illustrated in both Askew (1988) and Dijkstra and Lewington (2006). Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Note that the extracted colour values of dorsal dragonfly drawings from both sources are highly correlated. 3 Figure A3. Frequency distribution of the average colour lightness of 152 North American and 74 European dragonfly species. Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Rugs at the abscissa indicate the value of each species. Note that colour values are from different sources (North America: Needham et al. 2000, Europe: Askew 1988), and hence absolute values are not directly comparable. 4 Figure A4. Scatterplots of single ordinary least-squares regressions between average colour lightness of 8,127 North American dragonfly assemblages and mean temperature of the warmest quarter. Red dots represent assemblages that were excluded from the analysis because they contained less than five species. Note that those assemblages that were excluded scatter more than those with more than five species (c.f. the coefficients of determination) due to the inherent effect of very low sampling sizes. -
Odonatological Abstract Service
Odonatological Abstract Service published by the INTERNATIONAL DRAGONFLY FUND (IDF) in cooperation with the WORLDWIDE DRAGONFLY ASSOCIATION (WDA) Editors: Dr. Klaus Reinhardt, Dept Animal and Plant Sciences, University of Sheffield, Sheffield S10 2TN, UK. Tel. ++44 114 222 0105; E-mail: [email protected] Martin Schorr, Schulstr. 7B, D-54314 Zerf, Germany. Tel. ++49 (0)6587 1025; E-mail: [email protected] Dr. Milen Marinov, 7/160 Rossall Str., Merivale 8014, Christchurch, New Zealand. E-mail: [email protected] Published in Rheinfelden, Germany and printed in Trier, Germany. ISSN 1438-0269 years old) than old beaver ponds. These studies have 1997 concluded, based on waterfowl use only, that new bea- ver ponds are more productive for waterfowl than old 11030. Prejs, A.; Koperski, P.; Prejs, K. (1997): Food- beaver ponds. I tested the hypothesis that productivity web manipulation in a small, eutrophic Lake Wirbel, Po- in beaver ponds, in terms of macroinvertebrates and land: the effect of replacement of key predators on epi- water quality, declined with beaver pond succession. In phytic fauna. Hydrobiologia 342: 377-381. (in English) 1993 and 1994, fifteen and nine beaver ponds, respec- ["The effect of fish removal on the invertebrate fauna tively, of three different age groups (new, mid-aged, old) associated with Stratiotes aloides was studied in a shal- were sampled for invertebrates and water quality to low, eutrophic lake. The biomass of invertebrate preda- quantify differences among age groups. No significant tors was approximately 2.5 times higher in the inverte- differences (p < 0.05) were found in invertebrates or brate dominated year (1992) than in the fish-dominated water quality among different age classes. -
A Checklist of North American Odonata
A Checklist of North American Odonata Including English Name, Etymology, Type Locality, and Distribution Dennis R. Paulson and Sidney W. Dunkle 2009 Edition (updated 14 April 2009) A Checklist of North American Odonata Including English Name, Etymology, Type Locality, and Distribution 2009 Edition (updated 14 April 2009) Dennis R. Paulson1 and Sidney W. Dunkle2 Originally published as Occasional Paper No. 56, Slater Museum of Natural History, University of Puget Sound, June 1999; completely revised March 2009. Copyright © 2009 Dennis R. Paulson and Sidney W. Dunkle 2009 edition published by Jim Johnson Cover photo: Tramea carolina (Carolina Saddlebags), Cabin Lake, Aiken Co., South Carolina, 13 May 2008, Dennis Paulson. 1 1724 NE 98 Street, Seattle, WA 98115 2 8030 Lakeside Parkway, Apt. 8208, Tucson, AZ 85730 ABSTRACT The checklist includes all 457 species of North American Odonata considered valid at this time. For each species the original citation, English name, type locality, etymology of both scientific and English names, and approxi- mate distribution are given. Literature citations for original descriptions of all species are given in the appended list of references. INTRODUCTION Before the first edition of this checklist there was no re- Table 1. The families of North American Odonata, cent checklist of North American Odonata. Muttkows- with number of species. ki (1910) and Needham and Heywood (1929) are long out of date. The Zygoptera and Anisoptera were cov- Family Genera Species ered by Westfall and May (2006) and Needham, West- fall, and May (2000), respectively, but some changes Calopterygidae 2 8 in nomenclature have been made subsequently. Davies Lestidae 2 19 and Tobin (1984, 1985) listed the world odonate fauna Coenagrionidae 15 103 but did not include type localities or details of distri- Platystictidae 1 1 bution. -
2010 Animal Species of Concern
MONTANA NATURAL HERITAGE PROGRAM Animal Species of Concern Species List Last Updated 08/05/2010 219 Species of Concern 86 Potential Species of Concern All Records (no filtering) A program of the University of Montana and Natural Resource Information Systems, Montana State Library Introduction The Montana Natural Heritage Program (MTNHP) serves as the state's information source for animals, plants, and plant communities with a focus on species and communities that are rare, threatened, and/or have declining trends and as a result are at risk or potentially at risk of extirpation in Montana. This report on Montana Animal Species of Concern is produced jointly by the Montana Natural Heritage Program (MTNHP) and Montana Department of Fish, Wildlife, and Parks (MFWP). Montana Animal Species of Concern are native Montana animals that are considered to be "at risk" due to declining population trends, threats to their habitats, and/or restricted distribution. Also included in this report are Potential Animal Species of Concern -- animals for which current, often limited, information suggests potential vulnerability or for which additional data are needed before an accurate status assessment can be made. Over the last 200 years, 5 species with historic breeding ranges in Montana have been extirpated from the state; Woodland Caribou (Rangifer tarandus), Greater Prairie-Chicken (Tympanuchus cupido), Passenger Pigeon (Ectopistes migratorius), Pilose Crayfish (Pacifastacus gambelii), and Rocky Mountain Locust (Melanoplus spretus). Designation as a Montana Animal Species of Concern or Potential Animal Species of Concern is not a statutory or regulatory classification. Instead, these designations provide a basis for resource managers and decision-makers to make proactive decisions regarding species conservation and data collection priorities in order to avoid additional extirpations. -
Argia the News Journal of the Dragonfly Society of the Americas
ISSN 1061-8503 TheA News Journalrgia of the Dragonfly Society of the Americas Volume 22 17 December 2010 Number 4 Published by the Dragonfly Society of the Americas http://www.DragonflySocietyAmericas.org/ ARGIA Vol. 22, No. 4, 17 December 2010 In This Issue .................................................................................................................................................................1 Calendar of Events ......................................................................................................................................................1 Minutes of the 2010 Annual Meeting of the Dragonfly Society of the Americas, by Steve Valley ............................2 2010 Treasurer’s Report, by Jerrell J. Daigle ................................................................................................................2 Enallagma novaehispaniae Calvert (Neotropical Bluet), Another New Species for Arizona, by Rich Bailowitz ......3 Photos Needed ............................................................................................................................................................3 Lestes australis (Southern Spreadwing), New for Arizona, by Rich Bailowitz ...........................................................4 Ischnura barberi (Desert Forktail) Found in Oregon, by Jim Johnson ........................................................................4 Recent Discoveries in Montana, by Nathan S. Kohler ...............................................................................................5 -
Dragons and Damsels
Dragons and Damsels What are they really? Curator Emeritus of Entomology, Dr Rob Cannings The insect order Odonata (Greek for toothed jaws) contains the insects known in English as dragonflies. Two main groups live in BC. True dragonflies have hindwings broader than the forewings. When perched they hold their wings out away from the body. Damselflies are slimmer, often smaller and usually fly more slowly than dragonflies. At rest they usually hold their equal-sized wings together above the body. Western Forktail (Ischnura perparva) male. A common damselfly across southern BC. Photo: RBCM, G. Doerksen Dragonflies are some of the most ancient insects. They are far older than dinosaurs. Fossils of dragonfly ancestors are 300 to 350 million years old. Although they still have many primitive features, dragonflies are wonderfully adapted for their successful life as predators in the air. But, a dragonfly leads a double life – the immature stage, the larva, lives in water, camouflaged and mostly hidden. At this stage, before they can fly, its larva is an eager eater of small aquatic life. When it is time to mature, the larva emerges from the water and transforms into a flying adult. For thousands of years, dragonflies have caused superstitious fear in many people, even though they do not sting or bite humans. Maybe their boldness takes us aback, or their speed startles us. If you’ve never seen one, their strange appearance up close may seem fearsome. The English name dragonfly echoes the feelings these insects sometimes cause – they are the fanciful “devil’s darning needles” that sting venomously or sew up the lips. -
A Checklist of North American Odonata, 2021 1 Each Species Entry in the Checklist Is a Paragraph In- Table 2
A Checklist of North American Odonata Including English Name, Etymology, Type Locality, and Distribution Dennis R. Paulson and Sidney W. Dunkle 2021 Edition (updated 12 February 2021) A Checklist of North American Odonata Including English Name, Etymology, Type Locality, and Distribution 2021 Edition (updated 12 February 2021) Dennis R. Paulson1 and Sidney W. Dunkle2 Originally published as Occasional Paper No. 56, Slater Museum of Natural History, University of Puget Sound, June 1999; completely revised March 2009; updated February 2011, February 2012, October 2016, November 2018, and February 2021. Copyright © 2021 Dennis R. Paulson and Sidney W. Dunkle 2009, 2011, 2012, 2016, 2018, and 2021 editions published by Jim Johnson Cover photo: Male Calopteryx aequabilis, River Jewelwing, from Crab Creek, Grant County, Washington, 27 May 2020. Photo by Netta Smith. 1 1724 NE 98th Street, Seattle, WA 98115 2 8030 Lakeside Parkway, Apt. 8208, Tucson, AZ 85730 ABSTRACT The checklist includes all 471 species of North American Odonata (Canada and the continental United States) considered valid at this time. For each species the original citation, English name, type locality, etymology of both scientific and English names, and approximate distribution are given. Literature citations for original descriptions of all species are given in the appended list of references. INTRODUCTION We publish this as the most comprehensive checklist Table 1. The families of North American Odonata, of all of the North American Odonata. Muttkowski with number of species. (1910) and Needham and Heywood (1929) are long out of date. The Anisoptera and Zygoptera were cov- Family Genera Species ered by Needham, Westfall, and May (2014) and West- fall and May (2006), respectively.