Inventory of the Invertebrate Fauna at the Level of the Lake of Birds (North
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Water Beetles
Ireland Red List No. 1 Water beetles Ireland Red List No. 1: Water beetles G.N. Foster1, B.H. Nelson2 & Á. O Connor3 1 3 Eglinton Terrace, Ayr KA7 1JJ 2 Department of Natural Sciences, National Museums Northern Ireland 3 National Parks & Wildlife Service, Department of Environment, Heritage & Local Government Citation: Foster, G. N., Nelson, B. H. & O Connor, Á. (2009) Ireland Red List No. 1 – Water beetles. National Parks and Wildlife Service, Department of Environment, Heritage and Local Government, Dublin, Ireland. Cover images from top: Dryops similaris (© Roy Anderson); Gyrinus urinator, Hygrotus decoratus, Berosus signaticollis & Platambus maculatus (all © Jonty Denton) Ireland Red List Series Editors: N. Kingston & F. Marnell © National Parks and Wildlife Service 2009 ISSN 2009‐2016 Red list of Irish Water beetles 2009 ____________________________ CONTENTS ACKNOWLEDGEMENTS .................................................................................................................................... 1 EXECUTIVE SUMMARY...................................................................................................................................... 2 INTRODUCTION................................................................................................................................................ 3 NOMENCLATURE AND THE IRISH CHECKLIST................................................................................................ 3 COVERAGE ....................................................................................................................................................... -
Scope: Munis Entomology & Zoology Publishes a Wide Variety of Papers
_____________ Mun. Ent. Zool. Vol. 2, No. 1, January 2007___________ I MUNIS ENTOMOLOGY & ZOOLOGY Ankara / Turkey II _____________ Mun. Ent. Zool. Vol. 2, No. 1, January 2007___________ Scope: Munis Entomology & Zoology publishes a wide variety of papers on all aspects of Entomology and Zoology from all of the world, including mainly studies on systematics, taxonomy, nomenclature, fauna, biogeography, biodiversity, ecology, morphology, behavior, conservation, pa!eobiology and other aspects are appropriate topics for papers submitted to Munis Entomology & Zoology. Submission of Manuscripts: Works published or under consideration elsewhere (including on the internet) will not be accepted. At first submission, one double spaced hard copy (text and tables) with figures (may not be original) must be sent to the Editors, Dr. Hüseyin Özdikmen for publication in MEZ. All manuscripts should be submitted as Word file or PDF file in an e-mail attachment. If electronic submission is not possible due to limitations of electronic space at the sending or receiving ends, unavailability of e-mail, etc., we will accept ―hard‖ versions, in triplicate, accompanied by an electronic version stored in a floppy disk, a CD-ROM. Review Process: When submitting manuscripts, all authors provides the name, of at least three qualified experts (they also provide their address, subject fields and e-mails). Then, the editors send to experts to review the papers. The review process should normally be completed within 45-60 days. After reviewing papers by reviwers: Rejected papers are discarded. For accepted papers, authors are asked to modify their papers according to suggestions of the reviewers and editors. Final versions of manuscripts and figures are needed in a digital format. -
Foster, Warne, A
ISSN 0966 2235 LATISSIMUS NEWSLETTER OF THE BALFOUR-BROWNE CLUB Number Forty Five February 2020 Liopterus haemorrhoidalis (Fab.) found in a heathland pool in Dorset, England by Peter Sutton. ADDRESSES The addresses of authors of articles and reviewed works are mainly given at the end of this issue of Latissimus. The address for other correspondence is: Professor G N Foster, 3 Eglinton Terrace, Ayr KA7 1JJ, Scotland, UK – [email protected] 1 LATISSIMUS 45 February 2020 TOWARDS A PHOTOGUIDE FOR THE LARGER BRITISH WATER BEETLES Peter Sutton For some time now, I have been working on a sequel to The Larger Water Beetles of the British Isles (Sutton 2008) in a bid to photograph all of the large and spectacular aquatic Coleoptera of Britain. The trials and tribulations of the search for these fascinating insects are described in a recent article in British Wildlife (Sutton 2017). This article also reveals that some of the medium-sized species of interest, such as those of the genus Rhantus have been included, as have species from other groups, including the raft spider, Dolomedes plantarius (Clerck) and a rare wasp, Chalcis sispes (L.), parasitic on soldierflies (Stratiomyidae), which collectively highlight the conservation importance of some of the very special habitats in which they may be found. Figure 1 Rhantus frontalis (Marsham), brackish pool, Canvey Island, South Essex February 2020 LATISSIMUS 45 2 The prospective book, therefore, covers a good number of medium-sized water beetles (7- 13 mm), from the Piles Beetle Liopterus haemorrhoidalis (Fab.) (6.3-7.9 mm) to the comparatively large Ilybius ater (12.5 -14.5 mm), known by some in Britain as the Mud Dweller. -
Building-Up of a DNA Barcode Library for True Bugs (Insecta: Hemiptera: Heteroptera) of Germany Reveals Taxonomic Uncertainties and Surprises
Building-Up of a DNA Barcode Library for True Bugs (Insecta: Hemiptera: Heteroptera) of Germany Reveals Taxonomic Uncertainties and Surprises Michael J. Raupach1*, Lars Hendrich2*, Stefan M. Ku¨ chler3, Fabian Deister1,Je´rome Morinie`re4, Martin M. Gossner5 1 Molecular Taxonomy of Marine Organisms, German Center of Marine Biodiversity (DZMB), Senckenberg am Meer, Wilhelmshaven, Germany, 2 Sektion Insecta varia, Bavarian State Collection of Zoology (SNSB – ZSM), Mu¨nchen, Germany, 3 Department of Animal Ecology II, University of Bayreuth, Bayreuth, Germany, 4 Taxonomic coordinator – Barcoding Fauna Bavarica, Bavarian State Collection of Zoology (SNSB – ZSM), Mu¨nchen, Germany, 5 Terrestrial Ecology Research Group, Department of Ecology and Ecosystem Management, Technische Universita¨tMu¨nchen, Freising-Weihenstephan, Germany Abstract During the last few years, DNA barcoding has become an efficient method for the identification of species. In the case of insects, most published DNA barcoding studies focus on species of the Ephemeroptera, Trichoptera, Hymenoptera and especially Lepidoptera. In this study we test the efficiency of DNA barcoding for true bugs (Hemiptera: Heteroptera), an ecological and economical highly important as well as morphologically diverse insect taxon. As part of our study we analyzed DNA barcodes for 1742 specimens of 457 species, comprising 39 families of the Heteroptera. We found low nucleotide distances with a minimum pairwise K2P distance ,2.2% within 21 species pairs (39 species). For ten of these species pairs (18 species), minimum pairwise distances were zero. In contrast to this, deep intraspecific sequence divergences with maximum pairwise distances .2.2% were detected for 16 traditionally recognized and valid species. With a successful identification rate of 91.5% (418 species) our study emphasizes the use of DNA barcodes for the identification of true bugs and represents an important step in building-up a comprehensive barcode library for true bugs in Germany and Central Europe as well. -
The Effect of Geographical Scale of Sampling on DNA Barcoding
Syst. Biol. 61(5):851–869, 2012 c The Author(s) 2012. Published by Oxford University Press on behalf of Society of Systematic Biologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. DOI:10.1093/sysbio/sys037 Advance Access publication on March 7, 2012 The Effect of Geographical Scale of Sampling on DNA Barcoding 1,2,3 4 2,3 2,3 JOHANNES BERGSTEN ∗,DAVID T. BILTON ,TOMOCHIKA FUJISAWA ,MIRANDA ELLIOTT , MICHAEL T. MONAGHAN5,MICHAEL BALKE6,LARS HENDRICH6,JOJA GEIJER7,JAN HERRMANN7, GARTH N. FOSTER8,IGNACIO RIBERA9,ANDERS N. NILSSON10,TIMOTHY G. BARRACLOUGH3, AND ALFRIED P. VOGLER2,3 1Department of Entomology, Swedish Museum of Natural History, Box 50007, SE-104 05 Stockholm, Sweden; 2Entomology Department, Natural History Downloaded from https://academic.oup.com/sysbio/article-abstract/61/5/851/1736372 by guest on 20 November 2018 Museum, Cromwell road, London SW7 5BD, UK; 3Division of Biology, Imperial College London, Silwood Park Campus, Ascot SL5 7PY, UK; 4Marine Biology and Ecology Research Centre, School of Marine Science and Engineering, University of Plymouth, Drake Circus, Plymouth, Devon PL4 8AA, UK; 5Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Mueggelseedamm 301, 12587 Berlin, Germany; 6Zoologische Staatssammlung M¨unchen, M¨unchhausenstrasse21, 81247 M¨unchen,Germany; -
Antennal Sensory Structures in Water Bugs of Nepoidea (Insecta: Hemiptera: Nepomorpha), Their Morphology and Function
Zoomorphology (2019) 138:307–319 https://doi.org/10.1007/s00435-019-00446-4 ORIGINAL PAPER Antennal sensory structures in water bugs of Nepoidea (Insecta: Hemiptera: Nepomorpha), their morphology and function Agnieszka Nowińska1 · Jolanta Brożek1 Received: 2 January 2019 / Accepted: 30 April 2019 / Published online: 11 May 2019 © The Author(s) 2019 Abstract The Nepoidea superfamily belongs to the water bugs’ infraorder (Nepomorpha) and consists of two families—Belostoma- tidae and Nepidae. Species from those families are the largest of all nepomorphans and are considered to be top predators in aquatic ecosystems. A characteristic feature of the group is the existence of short antennae concealed in grooves behind the eyes, which is an adaptation to the water habitat. The antennae bear many types of sensillar structures, which receive signals from the environment. Among such structures, mechanosensilla were of the greatest diversity. The antennal sensilla of species from both families were examined under the scanning electron microscope. 11 essential morphological types of sensilla were distinguished, including 5 new mechanosensilla types (sensilla paddle-like, cone-like, squamiformia, brush-like and club-like). Basal types of mechanosensilla such as trichodea, chaetica, basiconica (subtype 1) and campaniformia occur in Nepoidea and other Heteroptera. In some representatives of both families, sensilla paddle-like and sensilla basiconica type 1 were observed. Moreover, sensilla chaetica and cone-like were found in some species of Belostomatidae, whereas in Nepidae sensilla squamiformia, brush-like and club-like were observed. Apart from mechanosensilla, one type of thermo- hygrosensilla (ampullacea) and two diferent shaped olfactory sensilla basiconica (subtypes 2, 3) and coeloconica (subtypes 1, 2, 3) were found. -
Special Publications Special
ARACHNIDS ASSOCIATED WITH WET PLAYAS IN THE SOUTHERN HIGH PLAINS WITH WET PLAYAS ARACHNIDS ASSOCIATED SPECIAL PUBLICATIONS Museum of Texas Tech University Number 54 2008 ARACHNIDS ASSOCIATED WITH WET PLAYAS IN THE SOUTHERN HIGH PLAINS (LLANO ESTACADO), C okendolpher et al. U.S.A. JAMES C. COKENDOLPHER, SHANNON M. TORRENCE, JAMES T. ANDERSON, W. DAVID SISSOM, NADINE DUPÉRRÉ, JAMES D. RAY & LOREN M. SMITH SPECIAL PUBLICATIONS Museum of Texas Tech University Number 54 Arachnids Associated with Wet Playas in the Southern High Plains (Llano Estacado), U.S.A. JAMES C. COKENDOLPHER , SHANNON M. TORREN C E , JAMES T. ANDERSON , W. DAVID SISSOM , NADINE DUPÉRRÉ , JAMES D. RAY , AND LOREN M. SMI T H Texas Tech University, Oklahoma State University, B&W Pantex, Texas Parks and Wildlife Department, West Texas A&M University, West Virginia University Layout and Design: Lisa Bradley Cover Design: James C. Cokendolpher et al. Copyright 2008, Museum of Texas Tech University All rights reserved. No portion of this book may be reproduced in any form or by any means, including electronic storage and retrieval systems, except by explicit, prior written permission of the publisher. This book was set in Times New Roman and printed on acid-free paper that meets the guidelines for permanence and durability of the Committee on Production Guidelines for Book Longevity of the Council on Library Resources. Printed: 10 April 2008 Library of Congress Cataloging-in-Publication Data Special Publications of the Museum of Texas Tech University, Number 54 Series Editor: Robert J. Baker Arachnids Associated with Wet Playas in the Southern High Plains (Llano Estacado), U.S.A. -
Acari: Prostigmata: Parasitengona) V
Acarina 16 (1): 3–19 © ACARINA 2008 CALYPTOSTASY: ITS ROLE IN THE DEVELOPMENT AND LIFE HISTORIES OF THE PARASITENGONE MITES (ACARI: PROSTIGMATA: PARASITENGONA) V. N. Belozerov St. Petersburg State University, Biological Research Institute, Stary Peterhof, 198504, RUSSIA, e-mail: [email protected] ABSTRACT: The paper presents a review of available data on some aspects of calyptostasy, i.e. the alternation of active (normal) and calyptostasic (regressive) stages that is characteristic of the life cycles in the parasitengone mites. There are two different, non- synonymous approaches to ontogenetic and ecological peculiarities of calyptostasy in the evaluation of this phenomenon and its significance for the development and life histories of Parasitengona. The majority of acarologists suggests the analogy between the alternating calyptostasy in Acari and the metamorphic development in holometabolous insects, and considers the calyptostase as a pupa-like stage. This is controversial with the opposite view emphasizing the differences between calyptostases and pupae in regard to peculiarities of moulting events at these stages. However both approaches imply the similar, all-level organismal reorganization at them. The same twofold approach concerns the ecological importance of calyptostasy, i.e. its organizing role in the parasitengone life cycles. The main (parasitological) approach is based on an affirmation of optimizing role of calyptostasy through acceleration of development for synchronization of hatching periods in the parasitic parasitengone larvae and their hosts, while the opposite (ecophysiological) approach considers the calyptostasy as an adaptation to climate seasonality itself through retaining the ability for developmental arrests at special calyptostasic stages evoked from normal active stages as a result of the life cycle oligomerization. -
Glasgow's Water Beetles
The Glasgow Naturalist (online 2012) Volume 25, Part 4. Urban biodiversity: Successes and Challenges Urban Biodiversity: Successes and Challenges: Glasgow’s water beetles Garth N. Foster The Aquatic Coleoptera Conservation Trust, 3 Eglinton Terrace, Ayr KA7 1JJ E-mail: [email protected] INTRODUCTION the list of 101 species recorded from 1990 onwards. Water beetles are a well-recorded freshwater group in However several water beetles specialising in pond Britain despite lacking the charisma of dragonflies and habitats have become established in the Glasgow area the angling interest of mayflies and the like. The over a similar period. conference on urban biodiversity held by the Glasgow Natural History Society in October 2010 provided the The following examples of some species in decline and stimulus to assess their status in the area. some on the increase serve to illustrate the range of habitats that can be occupied. Water beetles cannot be precisely excised from beetles Noterus clavicornis (De Geer) This species is usually as a whole. Coleoptera are divided into two major referred to as “The Large Noterus” because the name groups, the Adephaga and the Polyphaga. Within the clavicornis has also been applied to the smaller, Adephaga the name “Hydradephaga” has been coined flightless N. crassicornis (Müller), which is very rare to distinguish diving beetles and related species from in Scotland. The earliest Scottish record is a little the ground beetles in the Carabidae. This works fairly uncertain but by 1946 N. clavicornis was in the garden well so long as one ignores the fact that many ground of the greatest proponent of water beetles, Frank beetles are confined to aquatic emergent vegetation or Balfour-Browne, in Dumfriesshire and it was first to the water’s edge. -
The Flora and Fauna of the Northwich Woodlands
The Flora and Fauna of the Northwich Woodlands Compiled by Paul M Hill Last updated: 23 rd August 2010 CONTENTS Plants 4 Mosses 8 Fungi 9 Bryophytes 10 Lichens 10 Beetles 11 Bees, Ants and Wasps 13 Sawflies 13 Parasitic / Gall Waps 14 True Bugs 14 Planthoppers and Aphids 14 Mayflies 14 Scorpianflies 15 Lacewings 15 Stoneflies 15 Caddisflies 15 Flies 15 Micro-moths 20 Butterflies 24 Macro-moths 24 Dragonflies and Damselflies 27 Earwigs 27 Grasshopper, Crickets and Groundhoppers 28 Amphipods 28 Wood and Water Louse 28 Spiders 28 Mites 29 Centipedes and Millipedes 29 Leeches 29 Snails and Slugs 30 Birds 31 Mammals 33 Amphibians and Reptiles 33 BOTANICAL Plants Equisetum arvense............. Field Horsetail Phleum bertolonii................ Smaller Cat's-tail Equisetum palustre............. Marsh Horsetail Phleum pratense ................ Timothy Equisetum sylvaticum......... Wood Horsetail Phragmites australis ........... Common Reed Larix decidua ..................... European Larch Poa annua.......................... Annual Meadow-grass Pinus nigra......................... Austrian Pine / Corsican Poa compressa .................. Flattened Meadow-grass Pine Poa pratensis ..................... Smooth Meadow-grass Pinus sylvestris .................. Scots Pine Poa humilis......................... Spreading Meadow-grass Taxus baccata.................... Yew Poa trivialis......................... Rough Meadow-grass Taxodium distichum ........... Swamp Cypress Puccinellia distans.............. Reflexed Saltmarsh-grass Ophioglossum vulgatum.... -
The Effect of Geographical Scale of Sampling on DNA Barcoding
Systematic Biology Advance Access published April 16, 2012 c The Author(s) 2012. Published by Oxford University Press on behalf of Society of Systematic Biologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. DOI:10.1093/sysbio/sys037 The Effect of Geographical Scale of Sampling on DNA Barcoding 1,2,3 4 2,3 2,3 JOHANNES BERGSTEN ∗, DAVID T.BILTON , TOMOCHIKA FUJISAWA , MIRANDA ELLIOTT , MICHAEL T.MONAGHAN5, MICHAEL BALKE6, LARS HENDRICH6, JOJA GEIJER7, JAN HERRMANN7, GARTH N.FOSTER8, IGNACIO RIBERA9, ANDERS N.NILSSON10, TIMOTHY G.BARRACLOUGH3, AND ALFRIED P.VOGLER2,3 1Department of Entomology, Swedish Museum of Natural History, Box 50007, SE-104 05 Stockholm, Sweden; 2Entomology Department, Natural History Museum, Cromwell road, London SW7 5BD, UK; 3Division of Biology, Imperial College London, Silwood Park Campus, Ascot SL5 7PY, UK; 4Marine Biology and Ecology Research Centre, School of Marine Science and Engineering, University of Plymouth, Drake Circus, Plymouth, Devon PL4 8AA, UK; 5Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Mueggelseedamm 301, 12587 Berlin, Germany; 6Zoologische Staatssammlung M¨unchen, M¨unchhausenstrasse21, 81247 M¨unchen,Germany; 7School of Natural Sciences, Linnaeus University, SE-391 82 Kalmar, Sweden; 8The Aquatic Coleoptera Conservation Trust, 3 Eglinton Terrace, Ayr KA7 1JJ Scotland, UK; 9Institut de Biologia Evolutiva (CSIC-UPF), Passeig Mar´ıtimde la Barceloneta 37-49, 08003 Barcelona, Spain; and 10Department of Ecology and Environmental Science, Ume˚aUniversity, SE-90187 Ume˚a,Sweden; ∗Correspondence to be sent to: Department of Entomology, Swedish Museum of Natural History, Box 50007, SE-104 05 Stockholm, Sweden; E-mail: [email protected]. -
Reproducibility and Consistency of Proteomic Experiments on Natural Populations of a Non-Model Aquatic Insect
Reproducibility and Consistency of Proteomic Experiments on Natural Populations of a Non-Model Aquatic Insect Amparo Hidalgo-Galiana1*, Marta Monge2, David G. Biron3, Francesc Canals2, Ignacio Ribera1, Alexandra Cieslak1* 1 Animal Biodiversity and Evolution program, Institute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra), Barcelona, Spain, 2 Vall d’Hebron Institute of Oncology (VHIO) Edifici Collserola, Barcelona, Spain, 3 Laboratoire ‘‘Microorganismes: Ge´nome et Environnement’’, UMR CNRS 6023, Equipe Interactions hoˆtes-parasites, Universite´ Blaise Pascal, Aubie`re, France Abstract Population proteomics has a great potential to address evolutionary and ecological questions, but its use in wild populations of non-model organisms is hampered by uncontrolled sources of variation. Here we compare the response to temperature extremes of two geographically distant populations of a diving beetle species (Agabus ramblae) using 2-D DIGE. After one week of acclimation in the laboratory under standard conditions, a third of the specimens of each population were placed at either 4 or 27uC for 12 h, with another third left as a control. We then compared the protein expression level of three replicated samples of 2–3 specimens for each treatment. Within each population, variation between replicated samples of the same treatment was always lower than variation between treatments, except for some control samples that retained a wider range of expression levels. The two populations had a similar response, without significant differences in the number of protein spots over- or under-expressed in the pairwise comparisons between treatments. We identified exemplary proteins among those differently expressed between treatments, which proved to be proteins known to be related to thermal response or stress.