P E R L a Newsletter and Bibliography of the International Society of Plecopterologists
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Monte L. Bean Life Science Museum Brigham Young University Provo, Utah 84602 PBRIA a Newsletter for Plecopterologists
No. 10 1990/1991 Monte L. Bean Life Science Museum Brigham Young University Provo, Utah 84602 PBRIA A Newsletter for Plecopterologists EDITORS: Richard W, Baumann Monte L. Bean Life Science Museum Brigham Young University Provo, Utah 84602 Peter Zwick Limnologische Flußstation Max-Planck-Institut für Limnologie, Postfach 260, D-6407, Schlitz, West Germany EDITORIAL ASSISTANT: Bonnie Snow REPORT 3rd N orth A merican Stonefly S ymposium Boris Kondratieff hosted an enthusiastic group of plecopterologists in Fort Collins, Colorado during May 17-19, 1991. More than 30 papers and posters were presented and much fruitful discussion occurred. An enjoyable field trip to the Colorado Rockies took place on Sunday, May 19th, and the weather was excellent. Boris was such a good host that it was difficult to leave, but many participants traveled to Santa Fe, New Mexico to attend the annual meetings of the North American Benthological Society. Bill Stark gave us a way to remember this meeting by producing a T-shirt with a unique “Spirit Fly” design. ANNOUNCEMENT 11th International Stonefly Symposium Stan Szczytko has planned and organized an excellent symposium that will be held at the Tree Haven Biological Station, University of Wisconsin in Tomahawk, Wisconsin, USA. The registration cost of $300 includes lodging, meals, field trip and a T- Shirt. This is a real bargain so hopefully many colleagues and friends will come and participate in the symposium August 17-20, 1992. Stan has promised good weather and good friends even though he will not guarantee that stonefly adults will be collected during the field trip. Printed August 1992 1 OBITUARIES RODNEY L. -
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. -
Does Oxygen Limit Thermal Tolerance in Arthropods? a Critical Review of Current Evidence
Comparative Biochemistry and Physiology, Part A 192 (2016) 64–78 Contents lists available at ScienceDirect Comparative Biochemistry and Physiology, Part A journal homepage: www.elsevier.com/locate/cbpa Review Does oxygen limit thermal tolerance in arthropods? A critical review of current evidence Wilco C.E.P. Verberk a,⁎, Johannes Overgaard b,RasmusErnb,MarkBayleyb,TobiasWangb, Leigh Boardman c,JohnS.Terblanchec a Department of Animal Ecology and Ecophysiology, Radboud University Nijmegen, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands b Zoophysiology, Department of Bioscience, Aarhus University, C.F. Møllers Allé 3, Building 1131, DK-8000 Aarhus, Denmark c Department of Conservation Ecology and Entomology, Centre for Invasion Biology, Stellenbosch University, South Africa article info abstract Article history: Over the last decade, numerous studies have investigated the role of oxygen in setting thermal tolerance in aquatic an- Received 17 August 2015 imals, and there has been particular focus on arthropods. Arthropods comprise one of the most species-rich taxonomic Received in revised form 14 October 2015 groups on Earth, and display great diversity in the modes of ventilation, circulation, blood oxygen transport, with rep- Accepted 20 October 2015 resentatives living both in water (mainly crustaceans) and on land (mainly insects). The oxygen and capacity limita- Available online 24 October 2015 tion of thermal tolerance (OCLTT) hypothesis proposes that the temperature dependent performance curve of animals Keywords: is shaped by the capacity for oxygen delivery in relation to oxygen demand. If correct, oxygen limitation could provide OCLTT a mechanistic framework to understand and predict both current and future impacts of rapidly changing climate. Respiration physiology In arthropods, most studies testing the OCLTT hypothesis have considered tolerance to thermal extremes. -
Biological Effects of Secondary Salinisation on Freshwater Microinvertebrates in Tasmania:The Acute Salinity Toxicity Testing Of
BIOLOGICAL EFFECTS OF SECONDARY SALINISATION ON FRESHWATER MACROINVERTEBRATES IN TASMANIA: THE ACUTE SALINITY TOXICITY TESTING OF SEVEN MACROINVERTEBRATES. Kaylene Allan, B. Sc., Grad. Dip. Sc. Original photo courtesy of John Gooderham Submitted to the Department of Zoology, University of Tasmania in partial fulfilment of the requirements for the degree of Masters of Applied Science James Cook University Townsville, Queensland 2006 ACKNOWLEDGEMENTS I am grateful to Leon Barmuta and Peter Davies for their theoretical guidance throughout this project. I am especially grateful to Peter for his work collating and analysing the original field data that was used as the basis for this project, and to Leon for his assistance with the statistical analysis and review of the draft report. A special thank you also goes to Laurie Cook and Tom Sloane for their initial field, laboratory and taxonomic assistance, which made the rest of the project possible. Many other people have contributed to this project and I would like to sincerely thank: Ben Kefford for his encouragement, willingness to share his expertise and prompt replies to my questions no matter where he was; Wayne Kelly and Adam Stephens for providing assistance with materials and logistics; John Gooderham for his patient help with bug identification and permission to use photos from his and Edward Tsyrlin’s publication, “The Waterbug Book”; Christiane Smethurst, Bryony Townhill, Anne Watson, Dorothy McCartney and Lynne Reid who volunteered their time to assist with field work - a special thank you to Christiane for her brilliant bug-finding techniques and generous assistance; Sharon Moore for proof reading the draft report; Jon Marsden Smedley for his work on the study site map and information on field sites; people at DPIWE including, Kate Wilson, Colin Bastick, Tom Krasnicki, Martin Read and Marcus Hardie who provided data and information; and Garry Davidson, Mark Hocking and Kathryn Harris for providing literature. -
Nabs 2004 Final
CURRENT AND SELECTED BIBLIOGRAPHIES ON BENTHIC BIOLOGY 2004 Published August, 2005 North American Benthological Society 2 FOREWORD “Current and Selected Bibliographies on Benthic Biology” is published annu- ally for the members of the North American Benthological Society, and summarizes titles of articles published during the previous year. Pertinent titles prior to that year are also included if they have not been cited in previous reviews. I wish to thank each of the members of the NABS Literature Review Committee for providing bibliographic information for the 2004 NABS BIBLIOGRAPHY. I would also like to thank Elizabeth Wohlgemuth, INHS Librarian, and library assis- tants Anna FitzSimmons, Jessica Beverly, and Elizabeth Day, for their assistance in putting the 2004 bibliography together. Membership in the North American Benthological Society may be obtained by contacting Ms. Lucinda B. Johnson, Natural Resources Research Institute, Uni- versity of Minnesota, 5013 Miller Trunk Highway, Duluth, MN 55811. Phone: 218/720-4251. email:[email protected]. Dr. Donald W. Webb, Editor NABS Bibliography Illinois Natural History Survey Center for Biodiversity 607 East Peabody Drive Champaign, IL 61820 217/333-6846 e-mail: [email protected] 3 CONTENTS PERIPHYTON: Christine L. Weilhoefer, Environmental Science and Resources, Portland State University, Portland, O97207.................................5 ANNELIDA (Oligochaeta, etc.): Mark J. Wetzel, Center for Biodiversity, Illinois Natural History Survey, 607 East Peabody Drive, Champaign, IL 61820.................................................................................................................6 ANNELIDA (Hirudinea): Donald J. Klemm, Ecosystems Research Branch (MS-642), Ecological Exposure Research Division, National Exposure Re- search Laboratory, Office of Research & Development, U.S. Environmental Protection Agency, 26 W. Martin Luther King Dr., Cincinnati, OH 45268- 0001 and William E. -
A New Classification of the Order Perlaria
CAWTHRON INSTITUTE, NELSON, N. Z. A NEW CLASSIFICATION OF THE ORDER PERLARIA. BY R. J. TILLYARD. Reprinted from the Canadian Entomologist, February, 1921. rcin.org.pl rcin.org.pl CAWTHRON INSTITUTE, NELSON, N. Z. A NEW CLASSIFICATION OF THE ORDER PERLARIA. BY R. J. TILLYARD. Reprinted from the Canadian Entomologist, February, 1921. rcin.org.pl rcin.org.pl A NEW CLASSIFICATION OF THE ORDER PERLARIA. BY R. J. TILLYARD, M. A. Sc. D. (Cantab.) D. Sc. (Sydney), F. L. S., F. E. S., Chief of the Biological Department, Cawthron Institute of Scientific Research,. Nelson, New Zealand. For some years past I have been studying the Perlaria of Australia and New Zealand, about which little has been made known up to the present. Taken in connection with the forms already described from Southern Chile, Patagonia, Tierra del Fuego and the Subantartic Islands, these insects form a very distinct Notogaean Fauna, clearly marked off from the Perlaria of the Northern Hemis phere and of the Tropics by the fact that it is made up almost entirely of very archaic types. No representatives of the highly, specialized Perlidae (including Perlodidae) occur in these regions; no Pteronarcidae, in the strict sense in which that family will be defined in this paper; no Capniidae, Taeniopterygidae or Leuctridae; and only one or two isolated forms of Nemouridae (genus Udamocercia of Enderlein). In attempting to classify the known Notogaean forms of Perlaria, I have had recourse not only to all available imaginal characters, but also to as care ful a study of the individual life-histories as the rareness of most of the forms would permit. -
Systematic Revision of the Trans-Bassian Moriomorphine Genus
ZooKeys 1044: 339–373 (2021) A peer-reviewed open-access journal doi: 10.3897/zookeys.1044.62335 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae) James K. Liebherr1, Nick Porch2, Matthew Shaw3, Bronte E. Sinclair4, David R. Maddison5 1 Department of Entomology, John H. and Anna B. Comstock Hall, 129 Garden Ave., Cornell University, Ithaca, NY 14853-2601, USA 2 School of Life & Environmental Sciences & Centre for Integrated Ecology, Deakin University, Geelong, VIC 3216, Australia 3 South Australian Museum, South Terrace, Adelaide, SA 5000, Australia 4 Australian National Insect Collection, Building 101, Clunies Ross St., Black Mountain, ACT 2601, Australia 5 Department of Integrative Biology, Oregon State University, Corvallis, OR 97331, USA Corresponding author: James K. Liebherr ([email protected]) Academic editor: Thorsten Assmann | Received 21 December 2020 | Accepted 18 February 2021 | Published 16 June 2021 http://zoobank.org/8264C999-3201-4A3B-B39C-222790AC0192 Citation: Liebherr JK, N Porch, M Shaw, BE Sinclair, DR Maddison (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JK, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940–2020). ZooKeys 1044: 339–373. https://doi.org/10.3897/zookeys.1044.62335 Abstract The Australian genus Theprisa Moore, 1963, is taxonomically revised to comprise five species, two newly described: Theprisa darlingtoniLiebherr & Porch, sp. nov. of Tasmania, and Theprisa otway Liebherr, Porch & Maddison, sp. nov. from the Otway Ranges, Victoria. Two previously described species, T. -
Spatial and Phylogenetic Structure of DNA-Species of Alpine Stonefly
bioRxiv preprint doi: https://doi.org/10.1101/765578; this version posted September 11, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Spatial and phylogenetic structure of DNA-species of Alpine stonefly community 2 assemblages across seven habitats 3 4 Maribet Gamboa1, Joeselle Serrana1, Yasuhiro Takemon2, Michael T. Monaghan3, Kozo 5 Watanabe1 6 7 8 1Ehime University, Department of Civil and Environmental Engineering, Matsuyama, Japan 9 10 2Water Resources Research Center, Disaster Prevention Research Institute, Kyoto University, 11 6110011 Gokasho, Uji, Japan 12 13 3Leibniz-Institute of Freshwater Ecology and Inland Fisheries (IGB), Mueggelseedamm 301, 14 12587 Berlin, Germany 15 16 17 18 19 Correspondence 20 Kozo Watanabe, Ehime University, Department of Civil and Environmental Engineering, 21 Matsuyama, Japan. E-mail: [email protected] 22 bioRxiv preprint doi: https://doi.org/10.1101/765578; this version posted September 11, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 23 Abstract 24 1. Stream ecosystems are spatially heterogeneous environments due to the habitat diversity 25 that define different microhabitat patches within a single area. Despite the influence of 26 habitat heterogeneity on the biodiversity of insect community, little is known about how 27 habitat heterogeneity governs species coexistence and community assembly. -
Some Evolutionary Trends in Plecoptera
Some Evolutionary Trends in Plecoptera W. E. Ricker, Indiana University Structural Evolution The families and subfam ilies of stoneflies recognized by the writer are as follows: Distribution A. Suborder Holognatha (Setipalpia) Eustheniidae Eustheniinae Australia and New Zealand Diamphipnoinae Southern South America Austroperlidae Australia and New Zealand Leptoperlidae Leptoperlinae Australia and New Zealand; Fiji Islands; temperate South America Scopurinae Japan Peltoperlidae North and South America; east Asia and the bordering islands, south to Borneo Nemouridae Notonemourinae Australia and New Zealand Nemourinae Holarctic region Leuctrinae Holarctic region; South Africa; Tierra del Fuego Capniinae Holarctic Taeniopteryginae Holarctic Pteronarcidae North America; eastern Siberia B. Suborder Systellognatha (Filipalpia) Perlodidae Isogeninae Holarctic Perlodinae Holarctic Isoperlinae Holarctic Chloroperlidae Paraperlinae Nearctic Chloroperlinae Holarctic Perlidae Perlinae Old-world tropics, and the temperature regions of Africa, Eurasia and eastern North America Acroneuriinae North and South America; eastern and southeastern Asia 1 Contribution number 421 from the Department of Zoology, [ndiana University. 197 198 Indiana Academy of Science Tillyard places the ancestors of present day stoneflies in the family Lemmatophoridae of the Permian order Protoperlaria. These insects had small wing-like lateral expansions of the prothorax, and a fairly well- developed posterior (concave) median vein in both wings, both of which have been lost in modern stoneflies. Developments in some of the mor- phological features which have been most studied are as follows: Nymphal mouth parts: The holognathous families are characterized by bulky mandibles, by short thick palpi, and by having the paraglossae and glossae of the labium about equal in length. In the adult the man- dibles remain large and functional. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Butterflies of North America
Insects of Western North America 7. Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. 4. Hexapoda: Selected Coleoptera and Diptera with cumulative list of Arthropoda and additional taxa Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University, Fort Collins, CO 80523-1177 2 Insects of Western North America. 7. Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. 4. Hexapoda: Selected Coleoptera and Diptera with cumulative list of Arthropoda and additional taxa by Boris C. Kondratieff, Luke Myers, and Whitney S. Cranshaw C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 August 22, 2011 Contributions of the C.P. Gillette Museum of Arthropod Diversity. Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523-1177 3 Cover Photo Credits: Whitney S. Cranshaw. Females of the blow fly Cochliomyia macellaria (Fab.) laying eggs on an animal carcass on Fort Sill, Oklahoma. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins, Colorado, 80523-1177. Copyrighted 2011 4 Contents EXECUTIVE SUMMARY .............................................................................................................7 SUMMARY AND MANAGEMENT CONSIDERATIONS -
Otway Stonefly (Eusthenia Nothofagi)
#45 This Action Statement was first published in 1993 and remains current. This Otway Stonefly version has been prepared for web publication. It Eusthenia nothofagi retains the original text of the action statement, although contact information, the distribution map and the illustration may have been updated. © The State of Victoria, Department of Sustainability and Environment, 2003 Published by the Department of Sustainability and Environment, Victoria. Otway Stonefly (Eusthenia nothofagi) Distribution in Victoria (DSE 2002) 8 Nicholson Street, East Melbourne, Victoria 3002 Australia Description and Distribution Other stonefly nymphs which are either the The Otway Stonefly (Eusthenia nothofagi Otway Stonefly or the closely related This publication may be of Eusthenia venosa have been collected from assistance to you but the Zwick, 1979) is an insect (Order Plecoptera, West Arkin, Young and Ciancio creeks, and State of Victoria and its Family Eustheniidae) with a life cycle employees do not guarantee involving an aquatic nymph stage and a the Aire, Ford, Grey, Johanna, Parker and that the publication is terrestrial adult stage. Nymphs are brown- Erskine rivers. without flaw of any kind or green, with six pairs of blue-green gills on These streams pass through State forest, is wholly appropriate for abdominal segments 1 to 6. They can be State and National Park, and private land. your particular purposes found under rocks or on wood debris in The specimens are probably Otway and therefore disclaims all slow-flowing areas of streams in the Otway Stoneflies, as E. venosa is thought not to liability for any error, loss occur in the Otway Range, although this can or other consequence which Range, such as small pools and backwaters.