Aquatic Invertebrates?
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Bioindicators of Water Quality
Ephemeroptera | Mayflies ACE-11 Coleoptera | Beetles Using this guide Coleoptera with the data sheets Bioindicators of Water Quality Beetles Quick–Reference Guide Coleoptera (Beetles) Authors: Julie Speelman and Natalie Carroll | Photographer (unless otherwise noted): Julie Speelman | Design and Layout: Purdue Agricultural Communication Family Tolerance Number Family Tolerance 4 3 7 Value Found Score 5 5 5 Dryopidae 5 0 0 Dryopidae (larvae) Baetidae Baetiscidae Dytiscidae Dytiscidae (adult) Caenidae Dytiscidae 5 2 10 This publication shows aquatic insects that can be used as Long-toed Water Beetle Predaceous Diving Beetle Predaceous Diving Beetle Small Minnow Mayfly Armored Mayfly Small Square-gill Mayfly Biotic Water Quality Degree of Organic Elmidae 5 0 0 bioindicators of water quality in Indiana waterways. Bioindicators 5 are biological systems that are sensitive to environmental changes Index Rating Pollution Gyrinidae 4 0 0 organic pollution Dryopidae and, therefore, can indicate when pollution is present in the water. 0.00–3.75 excellent Long-toed Water Beetle Haliplidae 7 0 0 unlikely A tolerance score is included for each insect in this publication. Hydrophilidae 5 3 15 slight organic The tolerance score, ranging from 0–10, represents the insect’s 3.76–4.25 very good Psephenidae 4 0 0 sensitivity to pollution and can be used to estimate the quality of pollution possible the water in which the insect was found. Insects with a score of some organic Order Total 5 25 4.26–5.00 good 0 are intolerant to pollution, meaning they cannot tolerate any pollution probable water pollution, while insects with a score of 10 are very tolerant of fairly substantial 5 5 4 1 polluted water. -
Gustafson and Sites: D. Shorti a New Species of Whirligig
Gustafson and Sites: D. shorti a new species Grey Gustafson of whirligig beetle from the U.S. Department of Biology 167 Castetter Hall Annals of the Entomological Society of MSC03 2020 America 1 University of New Mexico Albuquerque, NM 87131-0001 Phone: 303-929-9606 Email: [email protected] ********************** PREPRINT FOR OPEN ACCESS *********************** A North American biodiversity hotspot gets richer: A new species of whirligig beetle from the Southeastern Coastal Plain of the United States Grey T. Gustafson1 and Robert W. Sites2 1Museum of Southwestern Biology, Department of Biology, University of New Mexico, Albuquerque, New Mexico 87131 U.S.A 2Enns Entomology Museum, Division of Plant Sciences, University of Missouri, Columbia, Missouri 65211, U.S.A. Abstract A new species of Dineutus Macleay, 1825 is described from the Southeastern Coastal Plain of the United Sates. Habitus and aedeagus images as well as illustrations of elytral apices, protarsus, palps, and male mesopretarsal claws are provided for Dineutus shorti n. sp. and compared to those of D. discolor Aubé, 1838. The importance of the Southeastern Coastal Plain as a biodiversity hotspot and the potential conservation concern of D. shorti n. sp. also are discussed. Keywords Aquatic beetle, new species, biodiversity, conservation, Southeastern Coastal Plain Introduction Whirligig beetles are commonly encountered aquatic beetles and are well known for their whirling swimming pattern (Tucker 1969) and propensity to form aggregates of hundreds to thousands of individuals (Heinrich and Vogt 1980). These beetles are especially abundant in the southeastern United States where all four genera known to occur in the U.S. can be found (Epler 2010). -
Antennal Lobe Architecture Across Coleoptera
RESEARCH ARTICLE Variations on a Theme: Antennal Lobe Architecture across Coleoptera Martin Kollmann1, Rovenna Schmidt1,2, Carsten M. Heuer1,3, Joachim Schachtner1* 1 Department of BiologyÐAnimal Physiology, Philipps-University Marburg, Marburg, Germany, 2 Institute of Veterinary Anatomy, Histology and Embryology, Justus-Liebig University Gieûen, Gieûen, Germany, 3 Fraunhofer-Institut fuÈr Naturwissenschaftlich-Technische Trendanalysen INT, Euskirchen, Germany * [email protected] a11111 Abstract Beetles comprise about 400,000 described species, nearly one third of all known animal species. The enormous success of the order Coleoptera is reflected by a rich diversity of life- styles, behaviors, morphological, and physiological adaptions. All these evolutionary adap- tions that have been driven by a variety of parameters over the last about 300 million years, OPEN ACCESS make the Coleoptera an ideal field to study the evolution of the brain on the interface Citation: Kollmann M, Schmidt R, Heuer CM, between the basic bauplan of the insect brain and the adaptions that occurred. In the current Schachtner J (2016) Variations on a Theme: study we concentrated on the paired antennal lobes (AL), the part of the brain that is typically Antennal Lobe Architecture across Coleoptera. PLoS ONE 11(12): e0166253. doi:10.1371/journal. responsible for the first processing of olfactory information collected from olfactory sensilla pone.0166253 on antenna and mouthparts. We analyzed 63 beetle species from 22 different families and -
ACTA ENTOMOLOGICA MUSEI NATIONALIS PRAGAE Nomenclatural Notes on Some Palaearctic Gyrinidae (Coleoptera)
ACTA ENTOMOLOGICA MUSEI NATIONALIS PRAGAE Published 15.xi.2016 Volume 56(2), pp. 645–663 ISSN 0374-1036 http://zoobank.org/urn:lsid:zoobank.org:pub:2C0E3A0A-8398-4BC3-BEBC-EA714FDC9F3D Nomenclatural notes on some Palaearctic Gyrinidae (Coleoptera) Hans FERY1) & Jiří HÁJEK2) 1) Räuschstraße 73, D-13509 Berlin, Germany; e-mail: [email protected] 2) Department of Entomology, National Museum, Cirkusová 1740, CZ-193 00 Praha 9 – Horní Počernice, Czech Republic; e-mail: [email protected] Abstract. Several names of Gyrinidae taxa have been found in the literature which are given with incorrect publishing dates. The correct data could be assigned to these taxa by specifying the true publishing dates mainly of fi ve important works: Aubé’s ‘Species général’ is dated September 29, 1838, and the third part of his ‘Iconographie’ December 31, 1838; Hatch’s ‘Phylogeny of Gyrinidae’ is dated 1926 instead of 1925; Modeer’s work on Gyrinidae is dated 1780 instead of 1776; Ochs’ works on Dineutini are dated again 1926 instead of 1927. Incorrectly cited publishing data of a few further works are also rectifi ed. Nomenclatural notes on several names in the family Gyrinidae are provided. These are on generic level Potamobius Stephens, 1829b, and Potamobius Hope, 1838, which are both juni- or subjective synonyms of Orectochilus Dejean, 1833 as well as junior primary homonyms of Potamobius Samouelle, 1819 (Decapoda), and thus they are perma- nently invalid. Five specifi c names were found to be junior primary homonyms. One of them, Gyrinus orientalis Régimbart, 1883 is replaced by Gyrinus mauricei nom. nov. Three names are not only junior homonyms, but also junior subjective synonyms, and thus no replacement name is currently needed: Gyrinus striatus Olivier, 1795, Gyrinus urinator Drapiez, 1819, and Gyrinus lineatus Lacordaire, 1835. -
Ancestral Gyrinidae Show Early Radiation of Beetles Before Permian-Triassic Mass Extinction Evgeny V
Yan et al. BMC Evolutionary Biology (2018) 18:33 https://doi.org/10.1186/s12862-018-1139-8 RESEARCH ARTICLE Open Access Whirling in the late Permian: ancestral Gyrinidae show early radiation of beetles before Permian-Triassic mass extinction Evgeny V. Yan1,2* , Rolf G. Beutel1 and John F. Lawrence3 Abstract Background: Gyrinidae are a charismatic group of highly specialized beetles, adapted for a unique lifestyle of swimming on the water surface. They prey on drowning insects and other small arthropods caught in the surface film. Studies based on morphological and molecular data suggest that gyrinids were the first branch splitting off in Adephaga, the second largest suborder of beetles. Despite its basal position within this lineage and a very peculiar morphology, earliest Gyrinidae were recorded not earlier than from the Upper Triassic. Results: Tunguskagyrus. with the single species Tunguskagyrus planus is described from Late Permian deposits of the Anakit area in Middle Siberia. The genus is assigned to the stemgroup of Gyrinidae, thus shifting back the minimum age of this taxon considerably: Tunguskagyrus demonstrates 250 million years of evolutionary stability for a very specialized lifestyle, with a number of key apomorphies characteristic for these epineuston predators and scavengers, but also with some preserved ancestral features not found in extant members of the family. It also implies that major splitting events in this suborder and in crown group Coleoptera had already occurred in the Permian. Gyrinidae and especially aquatic groups of Dytiscoidea flourished in the Mesozoic (for example Coptoclavidae and Dytiscidae) and most survive until the present day, despite the dramatic “Great Dying”–Permian-Triassic mass extinction, which took place shortly (in geological terms) after the time when Tunguskagyrus lived. -
Journal of the Society for British Entomology
ti J>- c . 6 7S. 7t HARVARD UNIVERSITY LIBRARY OF THE Museum of Comparative Zoology MBS. COW. Z30L Limy MHINtt UNIVERSITY HKTfflTZPi LiBnAi.il JUL 14 196 Journal UNIVERSITY OF THE Society for British Entomology World List abbreviation:^. Soc. Brit. Ent. VOL. 5 EDITED BY J. H. MURGATROYD, F.L.S., F.Z.S., F.R.E.S. E. J. POPHAM, D.Sc., Ph.D., A.R.C.S., F.R.E.S. WITH THE ASSISTANCE OF W. A. F. BALFOUR-BROWNE, M.A., F.R.S.E., F.L.S., F.Z.S., F.R.E.S., F.S.B.E. W. D. HINCKS, M.Sc.j F.R.E.S. B. M. HOBBY, M.A., D.Phil., F.R.E.S. G. J. KERRICH, M.A., F.L.S., F.R.E.S. O. W. RICHARDS, M.A., D.Sc., F.R.E.S., F.S.B.E. W. H. T. TAMS 1 955- 1 957 BOURNEMOUTH AND MANCHESTER DATES OF PUBLICATION Vol. 5 Part 1 (1-46). .14* July, 1954 Part 2 (47-90). .15th November, 1954 Part 3 (91-118). 1955 Part 4 (119-142). 1955 Part 5 (143-178). 1956 Part 6 (179-198). 1956 Part 7 (199-230). 1957 CONTENTS PAGE Andrewes, C. H.: Helocera delecta Mg. and other uncommon Diptera in the Isle of Wight. 164 Bailey, R.: Observations on the size of galls formed on couch grass by a Chalcidoid of the genus Harmolita. 199 Brown, William L., Jnr.: The identity of the British Strongylognathus (Hym. Formicidae). 113 Chambers, V. H.: Further Hymenoptera records from Bedfordshire. -
Sub-Functionalization of Dorsal and Ventral Eyes in a Whirligig Beetle (Coleoptera: Gyrinidae)
Neotropical Biodiversity ISSN: (Print) 2376-6808 (Online) Journal homepage: http://www.tandfonline.com/loi/tneo20 Sub-functionalization of dorsal and ventral eyes in a whirligig beetle (Coleoptera: Gyrinidae) David Andrés Salamanca & Federico Brown To cite this article: David Andrés Salamanca & Federico Brown (2018) Sub-functionalization of dorsal and ventral eyes in a whirligig beetle (Coleoptera: Gyrinidae), Neotropical Biodiversity, 4:1, 138-144, DOI: 10.1080/23766808.2018.1510567 To link to this article: https://doi.org/10.1080/23766808.2018.1510567 © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. Published online: 09 Sep 2018. Submit your article to this journal Article views: 115 View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=tneo20 NEOTROPICAL BIODIVERSITY 2018, VOL. 4, NO. 1, 138–144 https://doi.org/10.1080/23766808.2018.1510567 Sub-functionalization of dorsal and ventral eyes in a whirligig beetle (Coleoptera: Gyrinidae) David Andrés Salamancaa and Federico Brownb aIntegrative Zoology, Universitat Wien, Vienna, Austria; bZoology, Universidade de Sao Paulo, Sao Paulo, Brazil ABSTRACT ARTICLE HISTORY Compound eyes in nocturnal or fossorial insects generally express visible light opsins at Received 5 June 2017 higher levels than diurnal insects. In this study, we tested whether dorsal (above water) and Accepted 7 August 2018 ventral eyes (below water) of the diurnal four-eyed whirligig beetle Gyretes sericeus KEYWORDS Laboulbène, 1853, resemble opsin expression and function of diurnal or nocturnal insect Apposition; Gyretes; eyes respectively. By immunocytochemistry, we compared expression of green LW-opsin in rhodopsin; rhabdom; dorsal and ventral rhabdoms of whirligig beetle ommatidia. -
Coleoptera of Rye Bay
THE COLEOPTERA OF RYE BAY A SPECIALIST REPORT OF THE INTERREG II PROJECT TWO BAYS, ONE ENVIRONMENT a shared biodiversity with a common focus THIS PROJECT IS BEING PART-FINANCED BY THE EUROPEAN COMMUNITY European Regional Development Fund Dr. Barry Yates Patrick Triplet Peter J. Hodge SMACOPI 2 Watch Cottages 1,place de l’Amiral Courbet Winchelsea 80100 Abbeville East Sussex Picarde TN36 4LU [email protected] e-mail: [email protected] MARCH 2000 i ii The Coleoptera of Rye Bay This Specialist Report Contains Species Statements of 75 Red Data Book Coleoptera, the beetles. P.J.Hodge and B.J. Yates February 2000 Contents page number Introduction to the Two Bays Project 1 Coleoptera of Rye Bay 6 Coleoptera Species Statements Omophron limbatum (F., 1777) (Carabidae - a ground beetle) 8 Dyschirius angustatus (Ahrens, 1830) (Carabidae - a ground beetle) 9 Dyschirius obscurus (Gyllenhal, 1827) (Carabidae - a ground beetle) 10 Bembidion octomaculatum (Goeze, 1777) (Carabidae - a ground beetle) 11 Pogonus luridipennis (Germar, 1822) (Carabidae - a ground beetle) 12 Amara strenua (Zimmermann, 1832) (Carabidae - a ground beetle) 13 Harpalus parallelus (Dejean, 1829) (Carabidae - a ground beetle) 14 Badister collaris (Motschulsky) (Carabidae - a ground beetle) 15 Panagaeus cruxmajor (Linnaeus 1758) (Carabidae - a ground beetle) 16 Dromius vectensis (Rye, 1872) (Carabidae - a ground beetle) 17 Haliplus variegatus (Sturm, 1834) (Haliplidae - a water beetle) 18 Haliplus varius (Nicolai, 1822) (Haliplidae - a water beetle) 19 Laccophilus poecilus -
Chapter IX —Aquatic Coleoptera
Chapter IX —Aquatic Coleoptera (Beetles) • Insects of Inland Waters: Orders Having Aquatic Adults • (Williams & Feltmate, 1992) • Superphylum Arthropoda • (jointed-legged metazoan animals [Gr, arthron = joint; pous = foot]) • Phylum Entoma • Subphylum Uniramia • (L, unus = one; ramus = branch, referring to the unbranched nature of the ap- pendages) • Superclass Hexapoda • (Gr, hex = six, pous = foot) • Class Insecta • (L, insectum meaning cut into sections) • Subclass Ptilota • Infraclass Neopterygota Of the more than one million described species of insect, at least one-third are beetles, making the Coleoptera the most diverse order of living organisms. The order Coleoptera (beetles) is the largest order of insects. It belongs to the infraclass Neoptera, division Endopterygota. Members of this order have an anterior pair of wings (the elytra) that are hard and leathery and not used in flight; the membranous hindwings, which are used for flight, are concealed under the elytra when the animals are at rest. Only 10% of the 350,000 described species of beetles are aquatic. Aquatic species occur in two major suborders, the Adephaga and the Polyphaga. Both larvae and adults of six beetle families are aquatic, Dytiscidae (predaceous diving beetles), Elmidae (riffle beetles), Gyrinidae (whirligig beetles), Haliplidae (crawling water beetles), Hydrophilidae (water scavenger beetles), and Noteridae (burrowing water beetles). Five families, Chrysomelidae (leaf beetles), Limnichidae (marsh-loving beetles), Psephenidae (water pennies), Ptilodactylidae (toe- winged beetles), and Scirtidae (marsh beetles) have aquatic larvae and terrestrial adults, as do most of the other orders of aquatic insects; adult limnichids, however, readily submerge when disturbed. Three families have species that are terrestrial as larvae and aquatic as adults, Curculionidae (weevils), Dryopidae (long-toed water beetles), and Hydraenidae (moss beetles), a highly unusual combination among insects. -
Species Status No. 1: a Review of the Scarce and Threatened Coleoptera
Species Status No. 1 A review of the scarce and threatened Coleoptera of Great Britain Part 3: Water beetles of Great Britain by Garth N. Foster Further information on the JNCC Species Status project can be obtained from the Joint Nature Conservation Committee website at http://www.jncc.gov.uk/ Copyright JNCC 2010 ISSN 1473-0154 Water beetles of Great Britain This publication should be cited as: Foster, G.N. 2010. A review of the scarce and threatened Coleoptera of Great Britain Part (3): Water beetles of Great Britain. Species Status 1. Joint Nature Conservation Committee, Peterborough. 2 Water beetles of Great Britain Contents 1. Introduction to the Species Status series 6 1.1 The Species Status Assessment series 6 1.2 The Red List system 6 1.3 Status Assessments other than Red Lists for species in Britain 6 1.4 Species status assessment and conservation action 7 1.5 References 7 2. Introduction to this Review 9 2.1 World water beetles 9 2.2 Taxa considered in this Review 9 2.3 Previous reviews 9 3. The IUCN threat categories and selection criteria 10 3.1 The evolution of threat assessment methods 10 3.2 Summary of the 2001 categories and criteria 10 3.3 The two-stage process in relation to developing a Red List 13 3.4 The Near Threatened and Nationally Scarce categories 13 4. Methods and sources of information in this review 13 4.1 Introduction 13 4.2 Data sources 13 4.3 Amateur and professional entomologists 14 4.4 Collections 15 4.5 Near Threatened and Nationally Scarce categories 15 5. -
Burmese Amber Taxa
Burmese (Myanmar) amber taxa, on-line supplement v.2019.2 Andrew J. Ross 10/10/2019 Principal Curator of Palaeobiology Department of Natural Sciences National Museums Scotland Chambers St. Edinburgh EH1 1JF E-mail: [email protected] http://www.nms.ac.uk/collections-research/collections-departments/natural-sciences/palaeobiology/dr- andrew-ross/ This taxonomic list is a supplement to Ross (2019) and follows the same format. It includes taxa described or recorded from the beginning of 2019 up to the end of September 2019, plus a few that were published before then but were missed. Please note that only classes and orders which include new taxa or corrected records are listed below. A section has been added for trace fossils, which are not included in the taxon counts. Higher taxonomic changes: Dictyoptera are regarded as an order by Li (2019); birds (Aves) have been separated from non-avian theropods following Xing et al. (2019). New additions or changes to the published list (Ross, 2019) and supplement v.2019.1 are marked in blue, corrections are marked in red. Ross (2019) plus this supplement comprises 42 classes (or similar rank), 108 orders (or similar rank), 569 families, 1017 genera and 1379 species (excluding trace fossils, marine encrusters, Tilin amber and copal records). This includes 8 classes, 65 orders, 518 families, 942 genera and 1297 species of arthropods. Additional families rejected from occuring in Burmese amber- †Protopsyllidiidae Xyelidae Many thanks to everyone who has supplied pdfs of their papers. So that I can keep the list up-to-date please continue to send me your pdfs and let me know of any corrections required (particularly due to taxonomic changes) and references of papers in press. -
A Natural History of Conspecific Aggregations in Terrestrial Arthropods, with Emphasis on Cycloalexy in Leaf Beetles (Coleoptera: Chrysomelidae)
TAR Terrestrial Arthropod Reviews 5 (2012) 289–355 brill.com/tar A natural history of conspecific aggregations in terrestrial arthropods, with emphasis on cycloalexy in leaf beetles (Coleoptera: Chrysomelidae) Jorge A. Santiago-Blay1,*, Pierre Jolivet2,3 and Krishna K. Verma4 1Department of Paleobiology, MRC-121, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, DC 20013-7012, USA 2Natural History Museum, Paris, 67 Boulevard Soult, 75012 Paris, France 3Museum of Entomology, Florida State Collection of Arthropods Gainesville, FL, USA 4HIG 1/327, Housing Board Colony, Borsi, Durg-491001 India *Corresponding author; e-mails: [email protected], [email protected]. PJ: [email protected]; KKV: [email protected] Received on 30 April 2012. Accepted on 17 July 2012. Final version received on 29 October 2012. Summary Aggregations of conspecifics are ubiquitous in the biological world. In arthropods, such aggregations are generated and regulated through complex interactions of chemical and mechanical as well as abiotic and biotic factors. Aggregations are often functionally associated with facilitation of defense, thermomodula- tion, feeding, and reproduction, amongst others. Although the iconic aggregations of locusts, fireflies, and monarch butterflies come to mind, many other groups of arthropods also aggregate. Cycloalexy is a form of circular or quasicircular aggregation found in many animals. In terrestrial arthropods, cycloalexy appears to be a form of defensive aggregation although we cannot rule out other functions, particularly thermomodulation. In insects, cycloalexic-associated behaviors may include coordinated movements, such as the adoption of seemingly threatening postures, regurgitation of presumably toxic compounds, as well as biting movements. These behaviors appear to be associated with attempts to repel objects perceived to be threatening, such as potential predators or parasitoids.