Identifying the British Species of Leptophlebiidae
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Secondary Production of Paraleptophlebia (Ephemeroptera)
SECONDARY PRODUCTION OF PARALEPTOPHLEBIA (EPHEMEROPTERA) WITHIN THREE NORTHERN CALIFORNIA COASTAL STREAMS by Sarah Beesley A Thesis Presented to The Faculty of Humboldt State University In Partial Fulfillment Of the Requirements for the Degree Masters of Science In Natural Resources: Freshwater Fisheries November, 2006 ABSTRACT Secondary production of Paraleptophlebia (Ephemeroptera) within three northern California coastal streams Sarah Beesley Annual production was estimated for the mayfly genus Paraleptophlebia occupying riffle habitats of three coastal streams within the Prairie Creek watershed, California. Monthly invertebrate collections yielded 4,579 Paraleptophlebia nymphs: 1,786 from Prairie Creek, 1,738 from Boyes Creek and 1,055 from Streelow Creek. Paraleptophlebia populations in the three streams were presumed univoltine based on monthly size frequency distributions. Emergence appeared to occur from spring through fall with early instars present from late summer through spring. Models relating ln total length to ln dry mass and ln head width to ln dry mass were developed from fresh Prairie Creek Paraleptophlebia nymphs to estimate dry mass of preserved nymphs. Annual production estimates were 89.7 mg•m-2•yr-1 in Prairie Creek, 69.9 mg•m-2•yr-1 in Boyes Creek and 74.0 mg•m-2•yr-1 in Streelow Creek. Annual production to biomass ratios were 8.56 in Prairie Creek, 11.39 in Boyes Creek and 5.89 in Streelow Creek. Water temperature accumulation was monitored to assess whether differences in thermal regime existed among the three streams. Annual degree day totals were very similar among the streams with values from 3,447 in Streelow Creek, 3,473 in Prairie Creek, and 3,486 in Boyes Creek. -
Torix Rickettsia Are Widespread in Arthropods and Reflect a Neglected Symbiosis
GigaScience, 10, 2021, 1–19 doi: 10.1093/gigascience/giab021 RESEARCH RESEARCH Torix Rickettsia are widespread in arthropods and Downloaded from https://academic.oup.com/gigascience/article/10/3/giab021/6187866 by guest on 05 August 2021 reflect a neglected symbiosis Jack Pilgrim 1,*, Panupong Thongprem 1, Helen R. Davison 1, Stefanos Siozios 1, Matthew Baylis1,2, Evgeny V. Zakharov3, Sujeevan Ratnasingham 3, Jeremy R. deWaard3, Craig R. Macadam4,M. Alex Smith5 and Gregory D. D. Hurst 1 1Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Leahurst Campus, Chester High Road, Neston, Wirral CH64 7TE, UK; 2Health Protection Research Unit in Emerging and Zoonotic Infections, University of Liverpool, 8 West Derby Street, Liverpool L69 7BE, UK; 3Centre for Biodiversity Genomics, University of Guelph, 50 Stone Road East, Guelph, Ontario N1G2W1, Canada; 4Buglife – The Invertebrate Conservation Trust, Balallan House, 24 Allan Park, Stirling FK8 2QG, UK and 5Department of Integrative Biology, University of Guelph, Summerlee Science Complex, Guelph, Ontario N1G 2W1, Canada ∗Correspondence address. Jack Pilgrim, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK. E-mail: [email protected] http://orcid.org/0000-0002-2941-1482 Abstract Background: Rickettsia are intracellular bacteria best known as the causative agents of human and animal diseases. Although these medically important Rickettsia are often transmitted via haematophagous arthropods, other Rickettsia, such as those in the Torix group, appear to reside exclusively in invertebrates and protists with no secondary vertebrate host. Importantly, little is known about the diversity or host range of Torix group Rickettsia. -
Environmental Factors Affecting Mayfly Assemblages in Tufa-Depositing
Knowl. Manag. Aquat. Ecosyst. 2017, 418, 14 Knowledge & © M. Vilenica et al., Published by EDP Sciences 2017 Management of Aquatic DOI: 10.1051/kmae/2017005 Ecosystems www.kmae-journal.org Journal fully supported by Onema RESEARCH PAPER Environmental factors affecting mayfly assemblages in tufa-depositing habitats of the Dinaric Karst Marina Vilenica1,*, Vlatka Mičetić Stanković2, Michel Sartori3, Mladen Kučinić4 and Zlatko Mihaljević4 1 University of Zagreb, Faculty of Teacher Education, Trg Matice hrvatske 12, 44250 Petrinja, Croatia 2 Croatian Natural History Museum, Demetrova 1, 10000 Zagreb, Croatia 3 Museum of Zoology, Place de la Riponne 6, 1005 Lausanne, Switzerland 4 University of Zagreb, Faculty of Science, Rooseveltov trg 6, 10000 Zagreb, Croatia Abstract – Remarkably, unlike other parts of Europe, the ecology of mayflies in the southeastern regions is still poorly known. Here we present the first comprehensive study of Ephemeroptera in the tufa-depositing habitats of the Dinaric Karst. The study was conducted in Plitvice Lakes National Park monthly during a one-year period (2007–2008) in different types of habitats (springs, streams, mountainous rivers, tufa barriers). The aims of the study were to determine mayfly composition, abundance, spatial distribution and habitat preferences, and to examine the environmental factors important for the structuring of mayfly assemblages in Plitvice Lakes National Park. The mayfly fauna of tufa-depositing habitats was composed of 14 species (20 taxa). Water temperature, pH and ammonium concentration were the most important environmental variables explaining mayfly assemblages. Mayfly assemblages grouped according to habitat type. Generally, the most favourable habitat type was mountainous stream, tufa barriers were less favourable, and the least favourable were springs. -
MAYFLIES) Prepared by Terry Hitchings, Canterbury Museum – July 2003
National Centre for Aquatic Biodiversity and Biosecurity www.niwa.co.nz/ncabb CHECKLIST OF NEW ZEALAND EPHEMEROPTERA (MAYFLIES) Prepared by Terry Hitchings, Canterbury Museum – July 2003 AMELETOPSIDAE Ameletopsis perscitus Eaton, 1899 COLOBURISCIDAE Coloburiscus humeralis Walker, 1853 Coloburiscus tonnoiri Lestage, 1935 ICHTHYBOTIDAE Ichthybotus bicolor Tillyard, 1923 Ichthybotus hudsoni McLachlan, 1894 LEPTOPHLEBIIDAE Acanthophlebia cruentata Hudson, 1904 Arachnocolus phillipsi Towns & Peters, 1979 Atalophlebioides cromwelli Phillips, 1930 Austronella planulata Towns, 1983 Austroclima jollyae Towns & Peters, 1979 Austroclima sepia Phillips, 1930 Cryophlebia aucklandensis Peters, 1971 Deleatidium (Deleatidium) angustum Towns & Peters 1996 Deleatidium (Deleatidium) autumnale Phillips, 1930 Deleatidium (Deleatidium) cerinum Phillips, 1930 Deleatidium (Deleatidium) fumosum Phillips, 1930 Deleatidium (Deleatidium) lillii Eaton, 1899 Deleatidium (Deleatidium) magnum Towns & Peters, 1996 Deleatidium (Deleatidium) myzobranchia Phillips, 1930 Deleatidium (Penniketellum) cornutum Towns & Peters 1996 Deleatidium (Penniketellum) insolitum Towns & Peters, 1979 Deleatidium (Deleatidium) vernale Phillips, 1930 Isothraulus abditus Towns & Peters, 1979 Mauiulus aquilus Towns & Peters, 1996 Mauiulus luma Towns & Peters, 1979 Neozephlebia scita Walker, 1853 Tepakia caligata Towns & Peters, 1996 Zephlebia borealis Phillips, 1930 Zephlebia dentata Eaton, 1871 Zephlebia inconspicua Towns, 1983 Zephlebia nebulosa Towns & Peters, 1996 Zephlebia pirongia Towns -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
TB142: Mayflies of Maine: an Annotated Faunal List
The University of Maine DigitalCommons@UMaine Technical Bulletins Maine Agricultural and Forest Experiment Station 4-1-1991 TB142: Mayflies of aine:M An Annotated Faunal List Steven K. Burian K. Elizabeth Gibbs Follow this and additional works at: https://digitalcommons.library.umaine.edu/aes_techbulletin Part of the Entomology Commons Recommended Citation Burian, S.K., and K.E. Gibbs. 1991. Mayflies of Maine: An annotated faunal list. Maine Agricultural Experiment Station Technical Bulletin 142. This Article is brought to you for free and open access by DigitalCommons@UMaine. It has been accepted for inclusion in Technical Bulletins by an authorized administrator of DigitalCommons@UMaine. For more information, please contact [email protected]. ISSN 0734-9556 Mayflies of Maine: An Annotated Faunal List Steven K. Burian and K. Elizabeth Gibbs Technical Bulletin 142 April 1991 MAINE AGRICULTURAL EXPERIMENT STATION Mayflies of Maine: An Annotated Faunal List Steven K. Burian Assistant Professor Department of Biology, Southern Connecticut State University New Haven, CT 06515 and K. Elizabeth Gibbs Associate Professor Department of Entomology University of Maine Orono, Maine 04469 ACKNOWLEDGEMENTS Financial support for this project was provided by the State of Maine Departments of Environmental Protection, and Inland Fisheries and Wildlife; a University of Maine New England, Atlantic Provinces, and Quebec Fellow ship to S. K. Burian; and the Maine Agricultural Experiment Station. Dr. William L. Peters and Jan Peters, Florida A & M University, pro vided support and advice throughout the project and we especially appreci ated the opportunity for S.K. Burian to work in their laboratory and stay in their home in Tallahassee, Florida. -
Invertebrates
State Wildlife Action Plan Update Appendix A-5 Species of Greatest Conservation Need Fact Sheets INVERTEBRATES Conservation Status and Concern Biology and Life History Distribution and Abundance Habitat Needs Stressors Conservation Actions Needed Washington Department of Fish and Wildlife 2015 Appendix A-5 SGCN Invertebrates – Fact Sheets Table of Contents What is Included in Appendix A-5 1 MILLIPEDE 2 LESCHI’S MILLIPEDE (Leschius mcallisteri)........................................................................................................... 2 MAYFLIES 4 MAYFLIES (Ephemeroptera) ................................................................................................................................ 4 [unnamed] (Cinygmula gartrelli) .................................................................................................................... 4 [unnamed] (Paraleptophlebia falcula) ............................................................................................................ 4 [unnamed] (Paraleptophlebia jenseni) ............................................................................................................ 4 [unnamed] (Siphlonurus autumnalis) .............................................................................................................. 4 [unnamed] (Cinygmula gartrelli) .................................................................................................................... 4 [unnamed] (Paraleptophlebia falcula) ........................................................................................................... -
Final Report on Field Surveys
Ecological Surveys and Assessments to Facilitate Restoration Activities at the Salt River Marsh: Final Report on Field Surveys Prepared by: Peter J. Badra, Tyler J. Bassett, and Yu Man Lee Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901 For: Michigan Department of Environment, Great Lakes, and Energy, Water Resources Division February 4, 2020 Report Number 2020-05 Suggested Citation: Badra, P.J., T.J. Basset, Y.M. Lee. 2020. Ecological Surveys and Assessments to Facilitate Restoration Activities at the Salt River Marsh: Final Report on Field Surveys. Michigan Natural Features Inventory Report Number 2020-05, Lansing, MI. 97pp. Cover Photos: Background - Looking northwest at Stand 4, from edge of Stand 5, at cattails and common reed in the Salt River Marsh State Wildlife Area. Photo by Tyler J. Basset; Inset, left - Painted turtle hatchling. Photo by Yu Man Lee; Inset, right - American bluet damselfly larvae. Photo by Peter J. Badra. MSU is an affirmative-action, equal-opportunity employer. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, gender identity, religion, age, height, weight, disability, political beliefs, sexual orientation, marital status, family status or veteran status. Copyright 2020 MSU Board of Trustees Acknowledgments Financial support for this project was provided by the Great Lakes Restoration Initiative via the Water Resources Division of the Michigan Department of Environment, Great Lakes, and Energy. Daria Hyde and Ashley Cole-Wick provided essential assistance with the field component of this project. Thank you to the landowners who kindly allowed us to access the Salt River and marsh through their properties, especially during difficult times with high water. -
Research Paper Comparative Study of The
Internat. Rev. Hydrobiol. 95 2010 1 58–71 DOI: 10.1002/iroh.200811197 MANUEL JESÚS LÓPEZ-RODRÍGUEZ, JOSÉ MANUEL TIERNO DE FIGUEROA and JAVIER ALBA-TERCEDOR Departamento de Biología Animal. Facultad de Ciencias. Universidad de Granada. 18071, Granada, Spain; e-mail: [email protected] Research Paper Comparative Study of the Nymphal Biology of Two Coexisting Species of Mayflies (Insecta: Ephemeroptera) in a Mediterranean Stream in Southern Europe key words: mayflies, life cycle, feeding, secondary production, niche overlap Abstract We study the life history, nymphal feeding and secondary production of two leptophlebiid mayfly species (Habrophlebia eldae and Paraleptophlebia submarginata). They cohabit in a Mediterranean stream and present a very high niche overlap in terms of trophic resources. The life cycle was esti- mated using size-frequency analysis of samples taken throughout a year. Both species have a similar but displaced period of the nymphal development. Secondary production was calculated by means of the size-frequency method. Annual secondary production of P. submarginata is much higher than that of H. eldae (1.95 g DW m–2 year–1 vs. 0.17 g DW m–2 year–1), and presents a quite similar annual P/B ratio, but slightly higher in P. submarginata (6.97 in P. submarginata and 9.21 in H. eldae). The study of the gut contents revealed that they are mainly detritivores but, when larger they feed also on CPOM from leaves fallen in the stream. They present an almost total niche overlap in terms of food acquisition. However the previously mentioned shift in trophic resources utilization with size makes it possible that, because no similar size classes of each species are present at the same time, niche segregation exists between the two species. -
MAINE STREAM EXPLORERS Photo: Theb’S/FLCKR Photo
MAINE STREAM EXPLORERS Photo: TheB’s/FLCKR Photo: A treasure hunt to find healthy streams in Maine Authors Tom Danielson, Ph.D. ‐ Maine Department of Environmental Protection Kaila Danielson ‐ Kents Hill High School Katie Goodwin ‐ AmeriCorps Environmental Steward serving with the Maine Department of Environmental Protection Stream Explorers Coordinators Sally Stockwell ‐ Maine Audubon Hannah Young ‐ Maine Audubon Sarah Haggerty ‐ Maine Audubon Stream Explorers Partners Alanna Doughty ‐ Lakes Environmental Association Brie Holme ‐ Portland Water District Carina Brown ‐ Portland Water District Kristin Feindel ‐ Maine Department of Environmental Protection Maggie Welch ‐ Lakes Environmental Association Tom Danielson, Ph.D. ‐ Maine Department of Environmental Protection Image Credits This guide would not have been possible with the extremely talented naturalists that made these amazing photographs. These images were either open for non‐commercial use and/or were used by permission of the photographers. Please do not use these images for other purposes without contacting the photographers. Most images were edited by Kaila Danielson. Most images of macroinvertebrates were provided by Macroinvertebrates.org, with exception of the following images: Biodiversity Institute of Ontario ‐ Amphipod Brandon Woo (bugguide.net) – adult Alderfly (Sialis), adult water penny (Psephenus herricki) and adult water snipe fly (Atherix) Don Chandler (buigguide.net) ‐ Anax junius naiad Fresh Water Gastropods of North America – Amnicola and Ferrissia rivularis -
Distribution of Mayfly Species in North America List Compiled from Randolph, Robert Patrick
Page 1 of 19 Distribution of mayfly species in North America List compiled from Randolph, Robert Patrick. 2002. Atlas and biogeographic review of the North American mayflies (Ephemeroptera). PhD Dissertation, Department of Entomology, Purdue University. 514 pages and information presented at Xerces Mayfly Festival, Moscow, Idaho June, 9-12 2005 Acanthametropodidae Ameletus ludens Needham Acanthametropus pecatonica (Burks) Canada—ON,NS,PQ. USA—IL,GA,SC,WI. USA—CT,IN,KY,ME,MO,NY,OH,PA,WV. Ameletus majusculus Zloty Analetris eximia Edmunds Canada—AB. Canada—AB ,SA. USA—MT,OR,WA. USA—UT,WY. Ameletus minimus Zloty & Harper USA—OR. Ameletidae Ameletus oregonenesis McDunnough Ameletus amador Mayo Canada—AB ,BC,SA. Canada—AB. USA—ID,MT,OR,UT. USA—CA,OR. Ameletus pritchardi Zloty Ameletus andersoni Mayo Canada—AB,BC. USA—OR,WA. Ameletus quadratus Zloty & Harper Ameletus bellulus Zloty USA—OR. Canada—AB. Ameletus shepherdi Traver USA—MT. Canada—BC. Ameletus browni McDunnough USA—CA,MT,OR. Canada—PQ Ameletus similior McDunnough USA—ME,PA,VT. Canada—AB,BC. Ameletus celer McDunnough USA—CO,ID,MT,OR,UT Canada—AB ,BC. Ameletus sparsatus McDunnough USA—CO,ID,MT,UT Canada—AB,BC,NWT. Ameletus cooki McDunnough USA—AZ,CO,ID,MT,NM,OR Canada—AB,BC. Ameletus subnotatus Eaton USA—CO,ID,MT,OR,WA. Canada—AB,BC,MB,NB,NF,ON,PQ. Ameletus cryptostimulus Carle USA—CO,UT,WY. USA—NC,NY,PA,SC,TN,VA,VT,WV. Ameletus suffusus McDunnough Ameletus dissitus Eaton Canada—AB,BC. USA—CA,OR. USA—ID,OR. Ameletus doddsianus Zloty Ameletus tarteri Burrows USA—AZ,CO,NM,NV,UT. -
Aquatic Insects
AQUATIC INSECTS Challenges to Populations This page intentionally left blank AQUATIC INSECTS Challenges to Populations Proceedings of the Royal Entomological Society’s 24th Symposium Edited by Jill Lancaster Institute of Evolutionary Biology University of Edinburgh Edinburgh, UK and Robert A. Briers School of Life Sciences Napier University Edinburgh, UK CABI is a trading name of CAB International CABI Head Offi ce CABI North American Offi ce Nosworthy Way 875 Massachusetts Avenue Wallingford 7th Floor Oxfordshire OX10 8DE Cambridge, MA 02139 UK USA Tel: +44 (0)1491 832111 Tel: +1 617 395 4056 Fax: +44 (0)1491 833508 Fax: +1 617 354 6875 E-mail: [email protected] E-mail: [email protected] Website: www.cabi.org CAB International 2008. All rights reserved. No part of this publication may be reproduced in any form or by any means, electronically, mechanically, by photocopying, recording or otherwise, without the prior permission of the copyright owners. A catalogue record for this book is available from the British Library, London, UK. Library of Congress Cataloging-in-Publication Data Royal Entomological Society of London. Symposium (24th : 2007 : University of Edinburgh) Aquatic insects : challenges to populations : proceedings of the Royal Entomological Society’s 24th symposium / edited by Jill Lancaster, Rob A. Briers. p. cm. Includes bibliographical references and index. ISBN 978-1-84593-396-8 (alk. paper) 1. Aquatic insects--Congresses. I. Lancaster, Jill. II. Briers, Rob A. III. Title. QL472.R69 2007 595.7176--dc22 2008000626 ISBN: 978 1 84593 396 8 Typeset by AMA Dataset, Preston, UK Printed and bound in the UK by Cromwell Press, Trowbridge The paper used for the text pages in this book is FSC certifi ed.