Fly Times 43
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Diptera: Calyptratae)
Systematic Entomology (2020), DOI: 10.1111/syen.12443 Protein-encoding ultraconserved elements provide a new phylogenomic perspective of Oestroidea flies (Diptera: Calyptratae) ELIANA BUENAVENTURA1,2 , MICHAEL W. LLOYD2,3,JUAN MANUEL PERILLALÓPEZ4, VANESSA L. GONZÁLEZ2, ARIANNA THOMAS-CABIANCA5 andTORSTEN DIKOW2 1Museum für Naturkunde, Leibniz Institute for Evolution and Biodiversity Science, Berlin, Germany, 2National Museum of Natural History, Smithsonian Institution, Washington, DC, U.S.A., 3The Jackson Laboratory, Bar Harbor, ME, U.S.A., 4Department of Biological Sciences, Wright State University, Dayton, OH, U.S.A. and 5Department of Environmental Science and Natural Resources, University of Alicante, Alicante, Spain Abstract. The diverse superfamily Oestroidea with more than 15 000 known species includes among others blow flies, flesh flies, bot flies and the diverse tachinid flies. Oestroidea exhibit strikingly divergent morphological and ecological traits, but even with a variety of data sources and inferences there is no consensus on the relationships among major Oestroidea lineages. Phylogenomic inferences derived from targeted enrichment of ultraconserved elements or UCEs have emerged as a promising method for resolving difficult phylogenetic problems at varying timescales. To reconstruct phylogenetic relationships among families of Oestroidea, we obtained UCE loci exclusively derived from the transcribed portion of the genome, making them suitable for larger and more integrative phylogenomic studies using other genomic and transcriptomic resources. We analysed datasets containing 37–2077 UCE loci from 98 representatives of all oestroid families (except Ulurumyiidae and Mystacinobiidae) and seven calyptrate outgroups, with a total concatenated aligned length between 10 and 550 Mb. About 35% of the sampled taxa consisted of museum specimens (2–92 years old), of which 85% resulted in successful UCE enrichment. -
Wild Species 2010 the GENERAL STATUS of SPECIES in CANADA
Wild Species 2010 THE GENERAL STATUS OF SPECIES IN CANADA Canadian Endangered Species Conservation Council National General Status Working Group This report is a product from the collaboration of all provincial and territorial governments in Canada, and of the federal government. Canadian Endangered Species Conservation Council (CESCC). 2011. Wild Species 2010: The General Status of Species in Canada. National General Status Working Group: 302 pp. Available in French under title: Espèces sauvages 2010: La situation générale des espèces au Canada. ii Abstract Wild Species 2010 is the third report of the series after 2000 and 2005. The aim of the Wild Species series is to provide an overview on which species occur in Canada, in which provinces, territories or ocean regions they occur, and what is their status. Each species assessed in this report received a rank among the following categories: Extinct (0.2), Extirpated (0.1), At Risk (1), May Be At Risk (2), Sensitive (3), Secure (4), Undetermined (5), Not Assessed (6), Exotic (7) or Accidental (8). In the 2010 report, 11 950 species were assessed. Many taxonomic groups that were first assessed in the previous Wild Species reports were reassessed, such as vascular plants, freshwater mussels, odonates, butterflies, crayfishes, amphibians, reptiles, birds and mammals. Other taxonomic groups are assessed for the first time in the Wild Species 2010 report, namely lichens, mosses, spiders, predaceous diving beetles, ground beetles (including the reassessment of tiger beetles), lady beetles, bumblebees, black flies, horse flies, mosquitoes, and some selected macromoths. The overall results of this report show that the majority of Canada’s wild species are ranked Secure. -
Diptera: Tephritidae)
ANNALS OF THE UPPER SILESIAN MUSEUM IN BYTOM ENTOMOLOGY Vol. 28 (online 008): 1–9 ISSN 0867-1966, eISSN 2544-039X (online) Bytom, 17.12.2019 ANDRZEJ PALACZYK1 , ANNA KLASA2, ANDRZEJ SZLACHETKA3 First record in Poland and remarks on the origin of the northern populations of Goniglossum wiedemanni MEIGEN, 1826 (Diptera: Tephritidae) http://doi.org/10.5281/zenodo.3580897 1 Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Sławkowska 17, 31–016 Kraków, Poland, e-mail: [email protected] 2 Ojców National Park, 32–045 Sułoszowa, Ojców 9, e-mail: [email protected] 3 Parszowice 81, 59–330 Ścinawa, e-mail: [email protected] Abstract: The fruit fly Goniglossum wiedemanni has been recorded from Poland for the first time. Found in a single locality (Parszowice) in Lower Silesia, this species was recorded in a garden on Bryonia alba. Notes on the identification, biology and remarks on the general distribution and origin of the northern populations of this species are given. Colour photographs of the habitus and live specimens are also provided. Key words: Goniglossum wiedemanni, Carpomyini, species new for Poland, Lower Silesia, general distribution, Bryonia alba. INTRODUCTION Species from the family Tephritidae, the larvae of which develop in fruit, belong to the subfamilies Dacinae and Trypetinae. They occur most numerously in regions with a tropical or subtropical climate, where they pose a serious economic problem: in some areas they give rise to crop losses worth many millions of dollars. In central Europe, there are only a few species whose larvae feed on fruit; they belong exclusively to the tribes Carpomyini and Trypetini from the subfamily Trypetinae. -
Blow Fly (Diptera: Calliphoridae) in Thailand: Distribution, Morphological Identification and Medical Importance Appraisals
International Journal of Parasitology Research ISSN: 0975-3702 & E-ISSN: 0975-9182, Volume 4, Issue 1, 2012, pp.-57-64. Available online at http://www.bioinfo.in/contents.php?id=28. BLOW FLY (DIPTERA: CALLIPHORIDAE) IN THAILAND: DISTRIBUTION, MORPHOLOGICAL IDENTIFICATION AND MEDICAL IMPORTANCE APPRAISALS NOPHAWAN BUNCHU Department of Microbiology and Parasitology and Centre of Excellence in Medical Biotechnology, Faculty of Medical Science, Naresuan University, Muang, Phitsanulok, 65000, Thailand. *Corresponding Author: Email- [email protected] Received: April 03, 2012; Accepted: April 12, 2012 Abstract- The blow fly is considered to be a medically-important insect worldwide. This review is a compilation of the currently known occur- rence of blow fly species in Thailand, the fly’s medical importance and its morphological identification in all stages. So far, the 93 blow fly species identified belong to 9 subfamilies, including Subfamily Ameniinae, Calliphoridae, Luciliinae, Phumosiinae, Polleniinae, Bengaliinae, Auchmeromyiinae, Chrysomyinae and Rhiniinae. There are nine species including Chrysomya megacephala, Chrysomya chani, Chrysomya pinguis, Chrysomya bezziana, Achoetandrus rufifacies, Achoetandrus villeneuvi, Ceylonomyia nigripes, Hemipyrellia ligurriens and Lucilia cuprina, which have been documented already as medically important species in Thailand. According to all cited reports, C. megacephala is the most abundant species. Documents related to morphological identification of all stages of important blow fly species and their medical importance also are summarized, based upon reports from only Thailand. Keywords- Blow fly, Distribution, Identification, Medical Importance, Thailand Citation: Nophawan Bunchu (2012) Blow fly (Diptera: Calliphoridae) in Thailand: Distribution, Morphological Identification and Medical Im- portance Appraisals. International Journal of Parasitology Research, ISSN: 0975-3702 & E-ISSN: 0975-9182, Volume 4, Issue 1, pp.-57-64. -
Nomenclatural Studies Toward a World List of Diptera Genus-Group Names
Nomenclatural studies toward a world list of Diptera genus-group names. Part V Pierre-Justin-Marie Macquart Evenhuis, Neal L.; Pape, Thomas; Pont, Adrian C. DOI: 10.11646/zootaxa.4172.1.1 Publication date: 2016 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Evenhuis, N. L., Pape, T., & Pont, A. C. (2016). Nomenclatural studies toward a world list of Diptera genus- group names. Part V: Pierre-Justin-Marie Macquart. Magnolia Press. Zootaxa Vol. 4172 No. 1 https://doi.org/10.11646/zootaxa.4172.1.1 Download date: 02. Oct. 2021 Zootaxa 4172 (1): 001–211 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4172.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:22128906-32FA-4A80-85D6-10F114E81A7B ZOOTAXA 4172 Nomenclatural Studies Toward a World List of Diptera Genus-Group Names. Part V: Pierre-Justin-Marie Macquart NEAL L. EVENHUIS1, THOMAS PAPE2 & ADRIAN C. PONT3 1 J. Linsley Gressitt Center for Entomological Research, Bishop Museum, 1525 Bernice Street, Honolulu, Hawaii 96817-2704, USA. E-mail: [email protected] 2 Natural History Museum of Denmark, Universitetsparken 15, 2100 Copenhagen, Denmark. E-mail: [email protected] 3Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PW, UK. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by D. Whitmore: 15 Aug. 2016; published: 30 Sept. 2016 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 NEAL L. -
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. -
Changes in the Insect Fauna of a Deteriorating Riverine Sand Dune
., CHANGES IN THE INSECT FAUNA OF A DETERIORATING RIVERINE SAND DUNE COMMUNITY DURING 50 YEARS OF HUMAN EXPLOITATION J. A. Powell Department of Entomological Sciences University of California, Berkeley May , 1983 TABLE OF CONTENTS INTRODUCTION 1 HISTORY OF EXPLOITATION 4 HISTORY OF ENTOMOLOGICAL INVESTIGATIONS 7 INSECT FAUNA 10 Methods 10 ErRs s~lected for compar"ltive "lnBlysis 13 Bio1o~ica1 isl!lnd si~e 14 Inventory of sp~cies 14 Endemism 18 Extinctions 19 Species restricted to one of the two refu~e parcels 25 Possible recently colonized species 27 INSECT ASSOCIATES OF ERYSIMUM AND OENOTHERA 29 Poll i n!ltor<'l 29 Predqt,.n·s 32 SUMMARY 35 RECOm1ENDATIONS FOR RECOVERY ~4NAGEMENT 37 ACKNOWT.. EDGMENTS 42 LITERATURE CITED 44 APPENDICES 1. T'lbles 1-8 49 2. St::ttns of 15 Antioch Insects Listed in Notice of 75 Review by the U.S. Fish "l.nd Wildlife Service INTRODUCTION The sand dune formation east of Antioch, Contra Costa County, California, comprised the largest riverine dune system in California. Biogeographically, this formation was unique because it supported a northern extension of plants and animals of desert, rather than coastal, affinities. Geologists believe that the dunes were relicts of the most recent glaciation of the Sierra Nevada, probably originating 10,000 to 25,000 years ago, with the sand derived from the supratidal floodplain of the combined Sacramento and San Joaquin Rivers. The ice age climate in the area is thought to have been cold but arid. Presumably summertime winds sweeping through the Carquinez Strait across the glacial-age floodplains would have picked up the fine-grained sand and redeposited it to the east and southeast, thus creating the dune fields of eastern Contra Costa County. -
HOVERFLY NEWSLETTER Dipterists
HOVERFLY NUMBER 41 NEWSLETTER SPRING 2006 Dipterists Forum ISSN 1358-5029 As a new season begins, no doubt we are all hoping for a more productive recording year than we have had in the last three or so. Despite the frustration of recent seasons it is clear that national and international study of hoverflies is in good health, as witnessed by the success of the Leiden symposium and the Recording Scheme’s report (though the conundrum of the decline in UK records of difficult species is mystifying). New readers may wonder why the list of literature references from page 15 onwards covers publications for the year 2000 only. The reason for this is that for several issues nobody was available to compile these lists. Roger Morris kindly agreed to take on this task and to catch up for the missing years. Each newsletter for the present will include a list covering one complete year of the backlog, and since there are two newsletters per year the backlog will gradually be eliminated. Once again I thank all contributors and I welcome articles for future newsletters; these may be sent as email attachments, typed hard copy, manuscript or even dictated by phone, if you wish. Please do not forget the “Interesting Recent Records” feature, which is rather sparse in this issue. Copy for Hoverfly Newsletter No. 42 (which is expected to be issued with the Autumn 2006 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 2006. -
Flies) Benjamin Kongyeli Badii
Chapter Phylogeny and Functional Morphology of Diptera (Flies) Benjamin Kongyeli Badii Abstract The order Diptera includes all true flies. Members of this order are the most ecologically diverse and probably have a greater economic impact on humans than any other group of insects. The application of explicit methods of phylogenetic and morphological analysis has revealed weaknesses in the traditional classification of dipteran insects, but little progress has been made to achieve a robust, stable clas- sification that reflects evolutionary relationships and morphological adaptations for a more precise understanding of their developmental biology and behavioral ecol- ogy. The current status of Diptera phylogenetics is reviewed in this chapter. Also, key aspects of the morphology of the different life stages of the flies, particularly characters useful for taxonomic purposes and for an understanding of the group’s biology have been described with an emphasis on newer contributions and progress in understanding this important group of insects. Keywords: Tephritoidea, Diptera flies, Nematocera, Brachycera metamorphosis, larva 1. Introduction Phylogeny refers to the evolutionary history of a taxonomic group of organisms. Phylogeny is essential in understanding the biodiversity, genetics, evolution, and ecology among groups of organisms [1, 2]. Functional morphology involves the study of the relationships between the structure of an organism and the function of the various parts of an organism. The old adage “form follows function” is a guiding principle of functional morphology. It helps in understanding the ways in which body structures can be used to produce a wide variety of different behaviors, including moving, feeding, fighting, and reproducing. It thus, integrates concepts from physiology, evolution, anatomy and development, and synthesizes the diverse ways that biological and physical factors interact in the lives of organisms [3]. -
Identifying Bee-Flies in Genus Bombylius
Soldierflies and Allies Soldierflies and Allies Recording Scheme: Identifying bee-flies in genus Bombylius Compiled by Martin C. Harvey version 2, July 2014 In Britain there are four species of bee-fly in genus Bombylius, including perhaps the recording scheme’s most familiar fly: the Dark-edged Bee-fly Bombylius major. All four Bombylius have a long proboscis (‘tongue’) extending forward from the head, which they use to feed on nectar from flowering plants, often doing so while hovering over the flowers. They lay their eggs into the nests of solitary bees, where the bee-fly larvae prey on the bee larvae. The Dark-edged Bee-fly is by far the most frequently seen species, and is a familiar feature of early spring in gardens as well as countryside. In the south Dotted Bee-fly can also be numerous in suitable places. The other two species are smaller and rarer: the Western Bee-fly in a mix of habitats in western England and Wales, the Heath Bee-fly a specialist of heaths and largely confined to Dorset. Dark-edged Bee-fly, Bombylius major Dotted Bee-fly, Bombylius discolor Photos © Steven Falk Steven © Photos ♀ Solid dark band along front edge of wings Dark spots at ♂ junctions of wing veins Photo © Steven Falk Steven © Photo ♂ Main identification feature: check the dark edge Main identification feature: check the spots on to the wing (but wait until it stops flying to see the wings (but wait until it stops flying to see this!). this!). Body colour: mix of chestnut and black; female Body colour: looks evenly tawny-brown in flight. -
Diptera) Кавказа И ÂÅÑÒÍÈÊ Восточного Средиземноморья
161 162 All-Russian Institute of Plant Protection RAAS Справочный список и определитель родов и видов ISSN 1815-3682 хищных мух Dolichopodidae (Diptera) Кавказа и ÂÅÑÒÍÈÊ Восточного Средиземноморья. Гричанов И.Я. Санкт- ÇÀÙÈÒÛ ÐÀÑÒÅÍÈÉ Петербург: ВИЗР РАСХН, 2007, 160 c. (Приложение к Приложение журналу «Вестник защиты растений»). A checklist and keys to Dolichopodidae (Diptera) of the Caucasus and East Mediterranean. Igor Ya. Grichanov. St.Petersburg: VIZR RAAS, 2007, 160 p. (Plant Protection News, Supplement). Supplement Составлен справочный список (518 видов) и определитель 52 родов и 512 видов хищных мух Dolichopodidae (Diptera), известных на Кавказе A checklist and keys to (Азербайджан, Армения, Грузия; Россия: Ростовская область, Краснодар- ский и Ставропольский края, Адыгея, Алания, Дагестан, Кабардино- Dolichopodidae (Diptera) Балкария, Карачаево-Черкессия) и в странах Восточного Средиземноморья (Греция, Египет, Израиль, Ирак, Кипр, Молдавия, Сирия, Турция, Украина). Для каждого вида даны оригинальные родовые комбинации, of the Caucasus and East основные синонимы, глобальное распространение. Во вводном разделе приведены сведения о систематическом положении, морфологии, Mediterranean экологии и практическом значении имаго мух-зеленушек. Работа будет полезна специалистам – энтомологам и экологам, интересующимся энтомофагами, студентам и аспирантам учебных и научных учреждений. Igor Ya. GRICHANOV Рецензент: канд. биол. наук И.В. Шамшев Работа выполнялась в рамках ОНТП Россельхозакадемии (2001-2005, 2006-2010). Рекомендовано к печати -
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.