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A New Brachypterous Species of Elachiptera Becker (Diptera: Chloropidae) from Freshwater Wetlands in Eastern Canada
Zootaxa 360: 1–6 (2003) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 360 Copyright © 2003 Magnolia Press ISSN 1175-5334 (online edition) A new brachypterous species of Elachiptera Becker (Diptera: Chloropidae) from freshwater wetlands in eastern Canada TERRY A. WHEELER Department of Natural Resource Sciences, McGill University, Macdonald Campus, Ste-Anne-de-Bellevue, QC, H9X 3V9 CANADA ([email protected]) Abstract Elachiptera aquila sp. nov. is described from freshwater wetlands in Ontario and Quebec, Canada. Its apparent sister species is Elachiptera salinaria Sabrosky and Valley, known from coastal salt marshes in the eastern United States. Although there are Palearctic Elachiptera that are polymor- phic for wing length, this is the first brachypterous species of the genus described from North America. Key Words: Chloropidae, Diptera, Elachiptera, Nearctic, brachypterous, systematics Introduction Elachiptera Becker is one of the more easily recognized genera of Nearctic Chloropidae, primarily because of the broad, strap-like arista that characterizes most included species. Below the generic level, however, many species of Elachiptera are morphologically uni- form. One of the exceptions is Elachiptera salinaria Sabrosky and Valley, a salt marsh species from the eastern United States that can be easily distinguished from other Nearctic Elachiptera species by the broadly rounded occipital margin of the head (Sabrosky and Valley 1987). A new species, apparently closely related to E. salinaria, is described here from freshwater wetland habitats in eastern Canada. This is the first brachypterous species of Nearctic Elachiptera. Materials and Methods Specimens were initially preserved in 70% ethanol and subsequently prepared using a crit- ical-point dryer or chemically dried using hexamethyldisilazane. -
Functional Morphology and Evolution of the Sting Sheaths in Aculeata (Hymenoptera) 325-338 77 (2): 325– 338 2019
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Arthropod Systematics and Phylogeny Jahr/Year: 2019 Band/Volume: 77 Autor(en)/Author(s): Kumpanenko Alexander, Gladun Dmytro, Vilhelmsen Lars Artikel/Article: Functional morphology and evolution of the sting sheaths in Aculeata (Hymenoptera) 325-338 77 (2): 325– 338 2019 © Senckenberg Gesellschaft für Naturforschung, 2019. Functional morphology and evolution of the sting sheaths in Aculeata (Hymenoptera) , 1 1 2 Alexander Kumpanenko* , Dmytro Gladun & Lars Vilhelmsen 1 Institute for Evolutionary Ecology NAS Ukraine, 03143, Kyiv, 37 Lebedeva str., Ukraine; Alexander Kumpanenko* [[email protected]]; Dmytro Gladun [[email protected]] — 2 Natural History Museum of Denmark, SCIENCE, University of Copenhagen, Universitet- sparken 15, DK-2100, Denmark; Lars Vilhelmsen [[email protected]] — * Corresponding author Accepted on June 28, 2019. Published online at www.senckenberg.de/arthropod-systematics on September 17, 2019. Published in print on September 27, 2019. Editors in charge: Christian Schmidt & Klaus-Dieter Klass. Abstract. The sting of the Aculeata or stinging wasps is a modifed ovipositor; its function (killing or paralyzing prey, defense against predators) and the associated anatomical changes are apomorphic for Aculeata. The change in the purpose of the ovipositor/sting from being primarily an egg laying device to being primarily a weapon has resulted in modifcation of its handling that is supported by specifc morphological adaptations. Here, we focus on the sheaths of the sting (3rd valvulae = gonoplacs) in Aculeata, which do not penetrate and envenom the prey but are responsible for cleaning the ovipositor proper and protecting it from damage, identifcation of the substrate for stinging, and, in some taxa, contain glands that produce alarm pheromones. -
Diptera: Syrphidae)
Eur. J. Entomol. 110(4): 649–656, 2013 http://www.eje.cz/pdfs/110/4/649 ISSN 1210-5759 (print), 1802-8829 (online) Patterns in diurnal co-occurrence in an assemblage of hoverflies (Diptera: Syrphidae) 1, 2 2 1, 2 2 MANUELA D’AMEN *, DANIELE BIRTELE , LIVIA ZAPPONI and SÖNKE HARDERSEN 1 National Research Council, IBAF Department, Monterotondo Scalo, Rome, Italy; e-mails: [email protected]; [email protected] 2 Corpo Forestale dello Stato, Centro Nazionale Biodiversità Forestale “Bosco Fontana”, Verona, Italy; e-mails: [email protected]; [email protected] Key words. Diptera, Syrphidae, hoverflies, temporal structure, interspecific relations, null models Abstract. In this study we analyzed the inter-specific relationships in assemblages of syrphids at a site in northern Italy in order to determine whether there are patterns in diurnal co-occurrence. We adopted a null model approach and calculated two co-occurrence metrics, the C-score and variance ratio (V-ratio), both for the total catch and of the morning (8:00–13:00) and afternoon (13:00–18:00) catches separately, and for males and females. We recorded discordant species richness, abundance and co-occurrence patterns in the samples collected. Higher species richness and abundance were recorded in the morning, when the assemblage had an aggregated structure, which agrees with previous findings on communities of invertebrate primary consumers. A segregated pattern of co-occurrence was recorded in the afternoon, when fewer species and individuals were collected. The pattern recorded is likely to be caused by a number of factors, such as a greater availability of food in the morning, prevalence of hot and dry conditions in the early afternoon, which are unfavourable for hoverflies, and possibly competition with other pollinators. -
Newsletter of the Biological Survey of Canada
Newsletter of the Biological Survey of Canada Vol. 40(1) Summer 2021 The Newsletter of the BSC is published twice a year by the In this issue Biological Survey of Canada, an incorporated not-for-profit From the editor’s desk............2 group devoted to promoting biodiversity science in Canada. Membership..........................3 President’s report...................4 BSC Facebook & Twitter...........5 Reminder: 2021 AGM Contributing to the BSC The Annual General Meeting will be held on June 23, 2021 Newsletter............................5 Reminder: 2021 AGM..............6 Request for specimens: ........6 Feature Articles: Student Corner 1. City Nature Challenge Bioblitz Shawn Abraham: New Student 2021-The view from 53.5 °N, Liaison for the BSC..........................7 by Greg Pohl......................14 Mayflies (mainlyHexagenia sp., Ephemeroptera: Ephemeridae): an 2. Arthropod Survey at Fort Ellice, MB important food source for adult by Robert E. Wrigley & colleagues walleye in NW Ontario lakes, by A. ................................................18 Ricker-Held & D.Beresford................8 Project Updates New book on Staphylinids published Student Corner by J. Klimaszewski & colleagues......11 New Student Liaison: Assessment of Chironomidae (Dip- Shawn Abraham .............................7 tera) of Far Northern Ontario by A. Namayandeh & D. Beresford.......11 Mayflies (mainlyHexagenia sp., Ephemerop- New Project tera: Ephemeridae): an important food source Help GloWorm document the distribu- for adult walleye in NW Ontario lakes, tion & status of native earthworms in by A. Ricker-Held & D.Beresford................8 Canada, by H.Proctor & colleagues...12 Feature Articles 1. City Nature Challenge Bioblitz Tales from the Field: Take me to the River, by Todd Lawton ............................26 2021-The view from 53.5 °N, by Greg Pohl..............................14 2. -
Hoverfly Newsletter 34
HOVERFLY NUMBER 34 NEWSLETTER AUGUST 2002 ISSN 1358-5029 Long-standing readers of this newsletter may wonder what has happened to the lists of references to recent hoverfly literature that used to appear regularly in these pages. Graham Rotheray compiled these when he was editor and for some time afterwards, and more recently they have been provided by Kenn Watt. For some time Kenn trawled for someone else to take over this task from him, but nobody volunteered. Kenn continued to produce the lists, but now no longer has access to the source that provided him with the references. I therefore now make a plea for someone else to agree to take over this role, ideally producing a list of recent literature for each edition of this newsletter (i.e. twice per year), or if that is not possible, for each alternate edition. Failing a reply to this plea, has anyone any suggestions for a reliable source of references to which I could get access in order to compile the list myself? Copy for Hoverfly Newsletter No. 35 (which is expected to be issued in February 2003) should be sent to me: David Iliff, Green Willows, Station Road, Woodmancote, Cheltenham, Glos, GL52 9HN, Email [email protected], to reach me by 20 December. CONTENTS Stuart Ball Stubbs & Falk, second edition 2 Ted & Dave Levy News from the south-west, 2001 6 Kenneth Watt Flying over Finland: a search for rare saproxylic Diptera on the Aland Islands of Finland 7 Ted & Dave Levy Hoverflies at Coombe Dingle 8 David Iliff Field identification of some British hoverfly species using characteristics not included in the keys 10 Hoverflies of Northumberland 13 Interesting recent records 13 Second International Workshop on the Syrphidae: “Hoverflies: Biodiversity and Conservation” 14 Workshop Registration Form 15 1 STUBBS & FALK, SECOND EDITION Stuart G. -
Phylogeny of Syrphidae (Diptera) Inferred from Combined Analysis of Molecular and Morphological Characters
Systematic Entomology (2003) 28, 433–450 Phylogeny of Syrphidae (Diptera) inferred from combined analysis of molecular and morphological characters GUNILLA STA˚HLS1 , HEIKKI HIPPA2 , GRAHAM ROTHERAY3 , JYRKI MUONA1 andFRANCIS GILBERT4 1Finnish Museum of Natural History, University of Helsinki, Finland, 2Swedish Museum of Natural History, Stockholm, Sweden, 3National Museums of Scotland, Edinburgh, U.K. and 4School of Biological Sciences, Nottingham University, Nottingham, U.K. Abstract. Syrphidae (Diptera) commonly called hoverflies, includes more than 5000 species world-wide. The aim of this study was to address the systematic position of the disputed elements in the intrafamilial classification of Syrphidae, namely the monophyly of Eristalinae and the placement of Microdontini and Pipizini, as well as the position of particular genera (Nausigaster, Alipumilio, Spheginobaccha). Sequence data from nuclear 28S rRNA and mitochondrial COI genes in conjunction with larval and adult morphological characters of fifty-one syrphid taxa were analysed using optimization alignment to explore phylogenetic relationships among included taxa. A species of Platypezidae, Agathomyia unicolor, was used as outgroup, and also including one representative (Jassidophaga villosa) of the sister-group of Syrphidae, Pipunculidae. Sensitivity of the data was assessed under six different parameter values. A stability tree sum- marized the results. Microdontini, including Spheginobaccha, was placed basally, and Pipizini appeared as the sister-group to subfamily Syrphinae. The monophyly of subfamily Eristalinae was supported. The results support at least two independ- ent origins of entomophagy in syrphids, and frequent shifts between larval feeding habitats within the saprophagous eristalines. Introduction At the beginning of the last century, Syrphidae was divided into 2–20 subfamilies by different authors. -
Hoverfly Newsletter 67
Dipterists Forum Hoverfly Newsletter Number 67 Spring 2020 ISSN 1358-5029 . On 21 January 2020 I shall be attending a lecture at the University of Gloucester by Adam Hart entitled “The Insect Apocalypse” the subject of which will of course be one that matters to all of us. Spreading awareness of the jeopardy that insects are now facing can only be a good thing, as is the excellent number of articles that, despite this situation, readers have submitted for inclusion in this newsletter. The editorial of Hoverfly Newsletter No. 66 covered two subjects that are followed up in the current issue. One of these was the diminishing UK participation in the international Syrphidae symposia in recent years, but I am pleased to say that Jon Heal, who attended the most recent one, has addressed this matter below. Also the publication of two new illustrated hoverfly guides, from the Netherlands and Canada, were announced. Both are reviewed by Roger Morris in this newsletter. The Dutch book has already proved its value in my local area, by providing the confirmation that we now have Xanthogramma stackelbergi in Gloucestershire (taken at Pope’s Hill in June by John Phillips). Copy for Hoverfly Newsletter No. 68 (which is expected to be issued with the Autumn 2020 Dipterists Forum Bulletin) should be sent to me: David Iliff, Green Willows, Station Road, Woodmancote, Cheltenham, Glos, GL52 9HN, (telephone 01242 674398), email:[email protected], to reach me by 20 June 2020. The hoverfly illustrated at the top right of this page is a male Leucozona laternaria. -
Distribution of Oscinellinae (Diptera: Chloropidae) in the Danish Landscape Lise Brunberg Nielsen
Distribution of Oscinellinae (Diptera: Chloropidae) in the Danish landscape Lise Brunberg Nielsen Nielsen, Lise Brunberg: Distribution of Oscinellinae (Diptera: Chloropidae) in the Danish Landscape. Ent. Meddr 82: 39-62, Copenhagen, Denmark, 2014. ISSN 0013-8851 Abstract About 29,700 Oscinellinae were collected by means of sweep net, water traps and pitfalls in a variety of uncultivated habitats in Denmark mainly in Jutland. So far 75 species belonging to 21 genera are re corded from Denmark. Eleven species are new to the Danish fauna. Morphological details of Aphanotrigonum brachypterum, A. hungaricum, A. nigripes, Conioscinella gallarum, lncertella albipalpis, I. nigrifrons, I. kerteszi, I. scotica and Oscinella angustipennis are presented. The distribu tion of Oscinellinae in the Danish landscape is discussed. In Denmark, farmland dominates, so the two most abundant Oscinellarspecies of ara ble land, Oscinella frit and 0. vastator, are also predominant in most nat ural habitats. Small and larger uncultivated areas, however, making up only 25 % of the Danish landscape, contain a rich fauna of Oscinel lines. The advantage of different sampling methods combined is demonstrated. Sammendrag Fordelingen af fritf1uer (Diptera: Chloropidae) i det danske landskab. De fa millimeter lange, sorte eller sort-gule fritf1uer (Chloropidae) er nogle af de mest almindelige fluer pa gr<esarealer i Danmark. Et start materiale indsamlet med ketcher, i fangbakker og nedgravede fangglas pa forskellige udyrkede gr<esarealer er artsbestemt. Hovedparten af materialet, ea. 29.700 individer tilh0rer underfamilen Oscinellinae, der i Danmark omfatter 21 sl<egter og 75 arter. Elleve arter er nye for den danske fauna. Alle arter er beskrevet i Nartshuk & Andersson (2013), men supplerende morfologiske detaljer er her tilf0jet for 9 af dem: Aphanotrigonum brachypterum, A. -
Checklist of the Spider Wasps (Hymenoptera: Pompilidae) of British Columbia
Checklist of the Spider Wasps (Hymenoptera: Pompilidae) of British Columbia Scott Russell Spencer Entomological Collection Beaty Biodiversity Museum, UBC Vancouver, B.C. The family Pompilidae is a cosmopolitan group of some 5000 species of wasps which prey almost exclusively on spiders, giving rise to their common name - the spider wasps. While morphologically monotonous (Evans 1951b), these species range in size from a few millimetres long to among the largest of all hymenopterans; genus Pepsis, the tarantula hawks may reach up to 64 mm long in some tropical species (Vardy 2000). B.C.'s largest pompilid, Calopompilus pyrrhomelas, reaches a more modest body length of 19 mm among specimens held in our collection. In North America, pompilids are known primarily from hot, arid areas, although some species are known from the Yukon Territories and at least one species can overwinter above the snowline in the Colorado mountains (Evans 1997). In most species, the females hunt, attack, and paralyse spiders before laying one egg on (or more rarely, inside) the spider. Prey preferences in Pompilidae are generally based on size, but some groups are known to specialize, such as genus Ageniella on jumping spiders (Araneae: Salticidae) and Tachypompilus on wolf spiders (Araneae: Lycosidae) (Evans 1953). The paralysed host is then deposited in a burrow, which may have been appropriated from the spider, but is typically prepared before hunting from existing structures such as natural crevices, beetle tunnels, or cells belonging to other solitary wasps. While most pompilids follow this general pattern of behaviour, in the Nearctic region wasps of the genus Evagetes and the subfamily Ceropalinae exhibit cleptoparasitism (Evans 1953). -
Hymenoptera) with Highly Specialized Egg Morphology
Systematic Entomology (2011), 36, 529–548 Maxfischeriinae: a new braconid subfamily (Hymenoptera) with highly specialized egg morphology ∗ ∗ CHARLES ANDREW BORING1 , BARBARA J. SHARANOWSKI2 andMICHAEL J. SHARKEY1 1Department of Entomology, S-225 Agricultural Science Center North, University of Kentucky, Lexington, KY, U.S.A. and 2Department of Entomology, 214 Animal Science Bldg., University of Manitoba, Winnipeg, Canada Abstract. The tribe Maxfischeriini, previously placed in Helconinae, is emended to subfamily status based on morphological and biological evidence. Proposed autapomorphies for Maxfischeriinae include: the presence of a pronotal shelf, forewing vein 1a and 2a present, although 1a nebulous, ventral valve of the ovipositor with serrations from tip to base and specialized egg morphology. The novel, pedunculate egg morphology is described for Maxfischeria, representing a new life- history strategy among Braconidae. Based on egg and ovipositor morphology, we suggest that Maxfischeria is a proovigenic, koinobiont ectoparasitoid. Five new species of Maxfischeria Papp are described with an illustrated key to all species (Maxfischeria ameliae sp.n., Maxfischeria anic sp.n., Maxfischeria briggsi sp.n., Maxfischeria folkertsorum sp.n. and Maxfischeria ovumancora sp.n.). In addition to the identification key presented here, all known species of Maxfischeria can be separated using the barcoding region of cytochrome c oxidase subunit I (COI ). Based on molecular data, the phylogenetic relationships among the six known species of Maxfischeria are as follows: (M. folkertsorum sp.n. (M. ovumancora sp.n. (M. briggsi sp.n. (M. anic sp.n. (M. tricolor + M. ameliae sp.n.))))). Introduction in the forewing. However, Maxfischeria does not possess other features associated with Helconini, including a distinct Until now the braconid genus Maxfischeria included a lamella on the frons, two strongly developed lateral carinae single species, Maxfischeria tricolor Papp. -
Diptera) Diversity in a Patch of Costa Rican Cloud Forest: Why Inventory Is a Vital Science
Zootaxa 4402 (1): 053–090 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2018 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4402.1.3 http://zoobank.org/urn:lsid:zoobank.org:pub:C2FAF702-664B-4E21-B4AE-404F85210A12 Remarkable fly (Diptera) diversity in a patch of Costa Rican cloud forest: Why inventory is a vital science ART BORKENT1, BRIAN V. BROWN2, PETER H. ADLER3, DALTON DE SOUZA AMORIM4, KEVIN BARBER5, DANIEL BICKEL6, STEPHANIE BOUCHER7, SCOTT E. BROOKS8, JOHN BURGER9, Z.L. BURINGTON10, RENATO S. CAPELLARI11, DANIEL N.R. COSTA12, JEFFREY M. CUMMING8, GREG CURLER13, CARL W. DICK14, J.H. EPLER15, ERIC FISHER16, STEPHEN D. GAIMARI17, JON GELHAUS18, DAVID A. GRIMALDI19, JOHN HASH20, MARTIN HAUSER17, HEIKKI HIPPA21, SERGIO IBÁÑEZ- BERNAL22, MATHIAS JASCHHOF23, ELENA P. KAMENEVA24, PETER H. KERR17, VALERY KORNEYEV24, CHESLAVO A. KORYTKOWSKI†, GIAR-ANN KUNG2, GUNNAR MIKALSEN KVIFTE25, OWEN LONSDALE26, STEPHEN A. MARSHALL27, WAYNE N. MATHIS28, VERNER MICHELSEN29, STEFAN NAGLIS30, ALLEN L. NORRBOM31, STEVEN PAIERO27, THOMAS PAPE32, ALESSANDRE PEREIRA- COLAVITE33, MARC POLLET34, SABRINA ROCHEFORT7, ALESSANDRA RUNG17, JUSTIN B. RUNYON35, JADE SAVAGE36, VERA C. SILVA37, BRADLEY J. SINCLAIR38, JEFFREY H. SKEVINGTON8, JOHN O. STIREMAN III10, JOHN SWANN39, PEKKA VILKAMAA40, TERRY WHEELER††, TERRY WHITWORTH41, MARIA WONG2, D. MONTY WOOD8, NORMAN WOODLEY42, TIFFANY YAU27, THOMAS J. ZAVORTINK43 & MANUEL A. ZUMBADO44 †—deceased. Formerly with the Universidad de Panama ††—deceased. Formerly at McGill University, Canada 1. Research Associate, Royal British Columbia Museum and the American Museum of Natural History, 691-8th Ave. SE, Salmon Arm, BC, V1E 2C2, Canada. Email: [email protected] 2. -
Journal of Hymenoptera Research
c 3 Journal of Hymenoptera Research . .IV 6«** Volume 15, Number 2 October 2006 ISSN #1070-9428 CONTENTS BELOKOBYLSKIJ, S. A. and K. MAETO. A new species of the genus Parachremylus Granger (Hymenoptera: Braconidae), a parasitoid of Conopomorpha lychee pests (Lepidoptera: Gracillariidae) in Thailand 181 GIBSON, G. A. P., M. W. GATES, and G. D. BUNTIN. Parasitoids (Hymenoptera: Chalcidoidea) of the cabbage seedpod weevil (Coleoptera: Curculionidae) in Georgia, USA 187 V. Forest GILES, and J. S. ASCHER. A survey of the bees of the Black Rock Preserve, New York (Hymenoptera: Apoidea) 208 GUMOVSKY, A. V. The biology and morphology of Entedon sylvestris (Hymenoptera: Eulophidae), a larval endoparasitoid of Ceutorhynchus sisymbrii (Coleoptera: Curculionidae) 232 of KULA, R. R., G. ZOLNEROWICH, and C. J. FERGUSON. Phylogenetic analysis Chaenusa sensu lato (Hymenoptera: Braconidae) using mitochondrial NADH 1 dehydrogenase gene sequences 251 QUINTERO A., D. and R. A. CAMBRA T The genus Allotilla Schuster (Hymenoptera: Mutilli- dae): phylogenetic analysis of its relationships, first description of the female and new distribution records 270 RIZZO, M. C. and B. MASSA. Parasitism and sex ratio of the bedeguar gall wasp Diplolqjis 277 rosae (L.) (Hymenoptera: Cynipidae) in Sicily (Italy) VILHELMSEN, L. and L. KROGMANN. Skeletal anatomy of the mesosoma of Palaeomymar anomalum (Blood & Kryger, 1922) (Hymenoptera: Mymarommatidae) 290 WHARTON, R. A. The species of Stenmulopius Fischer (Hymenoptera: Braconidae, Opiinae) and the braconid sternaulus 316 (Continued on back cover) INTERNATIONAL SOCIETY OF HYMENOPTERISTS Organized 1982; Incorporated 1991 OFFICERS FOR 2006 Michael E. Schauff, President James Woolley, President-Elect Michael W. Gates, Secretary Justin O. Schmidt, Treasurer Gavin R.