Grootaert Debruyn Demeyer 1

Total Page:16

File Type:pdf, Size:1020Kb

Grootaert Debruyn Demeyer 1 151 Agromyzidae Agromyzidae Luc DE BRUYN & Michael VON TSCHIRNHAUS Agromyzidae, or leaf miners are small to very small, generally grey to black or brown, sometimes partially or completely yellow, flies. Costal vein of wing extending to apex of vein Mi+2 or reduced to the apex of vein R4+5, broken at apex of Ri (then sub-costa developed throughout its length and merging with vein Ri before reaching costa) or some distance before the point where Ri reaches the costa (then sub-costa fading distally, ending in costa well separated of vein Ri); basai crossvein always present, poste- rior crossvein frequently lacking; anal cell present. On the head normally between three and six orbital bristles, lower fronto-orbi- tals inclinated or missing (Selachops\ postverticals divergent; vibrissae mostly present. Third antennal segment usually rounded, shorter or slightly longer than broad, sometimes elongated or with a sharp point, somethimes greatly enlarged in males. Tibiae with¬ out preapical bristles; mid tibiae often with one to three posterolateral bristles; for tibiae rarely with one posterolateral bristle. Fe- male 7 abdominal tergite and sternite fused and chitinised into a non-retractile sheath for ovipositor, the latter with family spécifie teeth for drilling. Larvae of all agromyzid species are internai plant feeders with a family spécifie morphology. Most species are miners in leaves where they produce a characteristic form of mine, in most of the cases a substantial aid in identifying the agromyzid (Hering, 1935a&b, 1936, 1937a&b; key for European species in Hering, 1957). Some species are stem-borers, or develop in roots, seeds or galis. One genus develops exclusively in the cambium of young and old trees. Most species are monophagous, a considérable num- ber are oligophagous, while very few are truly polyphagous (Spencer, 1990). The Belgian Agromyzidae fauna has only been treated poorly until now. Most publications were usually limited to faunisti- cal lists (Jacobs, 1906) or some observations (Meunier, 1905, 1910-11; van den Buel; 1936, 1938; Collart, 1938, 1942; De Bruyn, 1988). Due to recent révisions of the family (e.g. Nowakowski, 1962), mainly based on the morphology of male genitalia, older faun- istical records are unreliable. General détermination keys can be found in Hendel (1931-36) and Spencer (1972,1976). Some genera are treated separate- ly in Spencer (1964, 1966), Nowakowski (1973), Griffiths (1980), but a reliable identification is only possible with the large num- ber of special publications, not yet included in général works. references; Jacobs (1906); Meunier (1905, 1910-11); Hendel (1931, 1931-36); Hering (1935, 1936, 1937a, 1937b, 1937c, 1951, 1957); van den Bruel (1936, 1938); Collart (1938,1942); Spencer (1964, 1966a, 1966b, 1972,1973,1976, 1990); Nowakow¬ ski (1962, 1973); Griffiths (1980); von Tschirnhaus (1981); De Bruyn (1988). Phytobia Lioy, 1864 lamii (Kaltenbach, 1858) Dendromyza Hendel, 1931 verbasci (Bouché, 1847) Liomyzina Enderlein, 1936 macquarti (Goureau, 1851) Liomycina Enderlein, 1936 Shizukoa Sasakawa, 1963 carbonaria (Zetterstedt, 1848) * Hexomyza Enderlein, 1936 schineri nigra (Zetterstedt, 1838) (Giraud, 1861) latigenis (Hendel, 1931) Melanagromyza Hendel, 1920 Amauromyza Hendel, 1931 Limnoagrorriyza Mal loch, 1921 Redia lioy, 1864 nee Filippi aeneoventris (Fallén, 1823) Cephalomyza Hendel, 1931 cirsii (Rondani, 1875) Trilobomyza Hendel, 1931 leucoptera (Czerny, 1909) Irenomyia Nowakowski, 1960 cunctans (Meigen, 1830) MelarwphytobiaHenng, 1960 Campanulomyza Nowakowski, 1962 Calalpomyza Spencer, 1977 (subge- Ophiomyia Braschnikov, 1897 nus) Tylomyza Hendel, 1931 AnnimyzellaSpencer, 1981 (subgenus) Stiropomyza Enderlein, 1936 Siphonomyza Enderlein, 1936 flavifrons (Meigen, 1830) Aulomyza Enderlein, 1936 labiatarum (Hendel, 1920) Siridomyza Enderlein, 1936 Agromyzidae 152 Solenomyza Enderlein, 1936 Praspedomyza Hendel, 1931 Stirops Enderlein, 1936 Triticomyza Blanchard, 1938 Triopisopa Enderlein, 1936 amoena (Meigen, 1830) Carinagromyza Sasakawa, 1954 artemisicola de Meijere, 1924 curvipalpis (Zcttcrstcdt, 1848) brunneicornis Hering, 1936 proboscidea (Strobl, 1900) bryoniae (Kaltenbach, 1858) prominens (Becker, 1908) solani Hering, 1927 achilleae Hering, 1937 mercurialis Hering, 1932 maura (Meigen, 1838) * citrulli Rohdendorf, 1950 asteris Kuroda, 1954 congesta (Becker, 1903) bicornis (Kaltenbach, 1869) leguminosarum de Meijere, 1924 pinguis (Fallén, 1820) minima Hendel, 1931 pulicaria (Meigen, 1830) parva Hendel, 1931 centaureana Hering, 1936 Agromyza Fallén, 1810 nigripleura Rydén, 1956 trifolii: authors Mesonevra Lioy, 1864 Slomacrypolus Enderlein, 1936 demeijerei Hering, 1930 Stomacrypeolus Enderlein, 1936 dianthicola (Venturi, 1949) Domomyza: authors eupatorii (Kaltenbach, 1873) alnibetulae Hendel, 1931 orbitella Hendel, 1931 flaviceps Fallén, 1823 flaveola (Fallén, 1823) nigripes Meigen, 1830 * lutea (Meigen, 1830) * agrosticola Hering, 1927 fulvella (Rondani, 1875) viridominalis Spencer, 1957 melanorhabda Hendel, 1931 potentillae (Kaltenbach, 1864) * pascuum (Meigen, 1838) * spiraeae Kaltenbach, 1867 pusilla (Meigen, 1830) * sanguisorbae Hendel, 1931 fasciola (Meigen, 1838) leucomaculataVimmet, 1931 sonchi Hendel, 1931 stackelbergi (Frey, 1946) erici Rydén, 1952 Angara (Meigen, 1830) * violae (Curtis, 1844) reptans Fallén, 1823 * taraxaci Hering, 1927 rondensis Strobl, 1900 ocellaris (Hendel, 1920) nigrifemur Hendel, 1931 Cerodontha Rondani, 1861 veris Hering, 1951 Cerodonta, emend. rufipes Meigen, 1830 Odontocera Macquart, 1835 buhriella Hering, 1954 Ceratomyza Schiner, 1862 Micromma sulfuriceps Strobl, 1898 Philippi, 1865 Crastemyza Nowakowski, 1967 montana Hendel, 1920 Dizygomyza Hendel, 1920 (subgenus) Phylagromyza Hendel, 1920 (subge¬ Phytoliriomyza Hendel, 1931 nus) Xyraeomyia Frick, 1952 Icteromyza Hendel, 1931 (subgenus) Lemurimyza Spencer, 1965 Poemyza Hendel, 1931 (subgenus) Pteridomyza Nowakowski, 1962 XenophytomyzaVrey, 1946 (subgenus) Nesomyza Spencer, 1973 Butomomyza Nowakowski, 1967 (sub¬ melampyga (Loew, 1869) genus) impaiientis (Brischke, 1881) bimaculata (Meigen, 1830) variegata (Meigen, 1830) * basilaris (Meigen, 1838) laterella (Zetterstedt, 1838) flavocincta (Strobl, 1880) Metopomyza Enderlein, 1936 denticornis (Panzer, 1806) * ornata (Meigen, 1830) * meigenii (Fallén, 1823) elegantula (Zetterstedt, 1848) nigritarsis {Meigen, 1830) limbatella (Zetterstedt, 1848) acuticornis (Meigen, 1830) confinis (Meigen, 1830) Liriomyza MIK, 1894 tarsella (Zetterstedt, 1848) Agrophila Lioy, 1864 nee Boisduval nigriventris (Strobl, 1900) Haplomyza Hendel, 1914 nigroscutellata (Strobl, 1900) semivittata Antineura Meiander, 1913 nee Osten (Strobl, 1909) Sacken flavicornis (Egger, 1862) * 153 Agromyzidae fulvipes (Meigen, 1830) * albiceps Meigen, 1830 * occulta (Meigen, 1838) flavoantennata Strobl, 1898 iraeos (Robineau-Desvoidy, 1851) rydeniana Hering, 1949 ircosr. error angelicastri Hering, 1932 ireos (Goureau, 1851) aquilegiae Hardy, 1849 luctuosa (Meigen, 1830) * calthophilaYlenng, 1931 effusi (Karl, 1926) chaerophylli Kaltenbach, 1856 morosa (Meigen, 1830) anthrisci Hendel, 1924 grossicornis (Zetterstedt, 1860) coniophila Hering, 1931 soenderupiFrey, 1950 (misidentifica- daucivora Hering, 1931 tion) aromatici Hering, 1931 conopodii Hering, 1943 Calycomyza Hendel, 1931 cichorii Spencer, 1966 artemisiae (Kaltenbach, 1856) cytisi Brischke, 1881 atripes (Zetterstedt, 1860) eupatorii Hendel, 1927 atripes (Brischke, 1880) flavicornis Fallén, 1823 * humeralis{\on Roser, 1840) glechomae Kaltenbach, 1862 bellidis (Kaltenbach, 1858) piceipes (van der Wulp, 1871) ilicis Curtis, 1846 * Paraphytomyza Enderlein, 1936 aquifolii Goureau, 1851 Aulagromyza Enderlein, 1936 lappae Goureau, 1851 R ubiomyza Nowakowski, 1962 lappirui Goureau, 1851 Phytagromyza: authors arctii (Kaltenbach, 1856) luteoscutellata (de Meijere, 1924) lonicerae Robinneau-Desvoidy, 1851 falleni (Rydén, 1952) xylostei Kaltenbach, 1862 lonicerarum (Frey, 1946) harlemensis Weyenbergh, 1870 lonicerae xylostei Hendel, 1932 Brischke, 1881 soenderupiana (Rydén, 1958) tridentata (Loew, 1858) minuscula Goureau, 1851 ancholiae Goureau, 1851 Napomyza Westwood, 1840 aquilegiae Robineau-Desvoidy, 1851 NapomyzaCurtis, 1837 nigripennis Fallén, 1823 * Dinevra Lioy, 1864 obscurella Fallén, 1823 * albipennis (Fallén, 1823) * pubicornis Hendel, 1920 cichorii Spencer, 1966 ranunculi (Schrank, 1803) * elegans (Meigen, 1830) flaveola Fallén, 1810 fesliva (Meigen, 1830) flava Fallén, 1823 lateralis (Fallén, 1823) flavoscutellataVaWén, 1823 albipes Meigen, 1830 scutellata Chromatomyia Hardy, 1849 Meigen, 1830 praecox Meigen, 1830 asteris Hendel, 1934 vitripennis Meigen, 1830 horticola (Goureau, 1851) * terminalis Meigen, 1830 cucumidis Macquart, 1854 pallida Meigen, 1830 tropaeoli Dufour, 1857 maculipes Brullé, 1832 fediae Kaltenbach, 1860 incisa Macquart, 1835 linariae Kaltenbach, 1862 citrinavon Roser, 1840 pisi Kaltenbach, 1864 maculipes Zetterstedt, 1848 nee Brullé lactucae (Vimmer, 1926) cinereovittata Zetterstedt, 1848 milii (Kaltenbach, 1864) * ranunculi Robineau-Desvoidy, 1851 nigra (Meigen, 1830) * nee Schrank zeitersledtii cinereofrons Hardy, 1849 Schiner, 1864 ranunculi Kaltenbach, 1867 nee periclymeni (de Meijere, 1924) Schrank, nee Robineau-Desvoidy primulae Robineau-Desvoidy, 1851 flavotibialis Strobl, 1902 islandica Rydén, 1953 Phytomyza Fallén, 1810 pentalinearis Kuroda, 1954 tenuipennis Singh & Ipe, 1973 affinis Fallén, 1823 * scolopendrii Goureau, 1851 agromyzina Meigen, 1830 elegans Goureau, 1851 similis Brischke,
Recommended publications
  • Dipterists Digest
    Dipterists Digest 2019 Vol. 26 No. 1 Cover illustration: Eliozeta pellucens (Fallén, 1820), male (Tachinidae) . PORTUGAL: Póvoa Dão, Silgueiros, Viseu, N 40º 32' 59.81" / W 7º 56' 39.00", 10 June 2011, leg. Jorge Almeida (photo by Chris Raper). The first British record of this species is reported in the article by Ivan Perry (pp. 61-62). Dipterists Digest Vol. 26 No. 1 Second Series 2019 th Published 28 June 2019 Published by ISSN 0953-7260 Dipterists Digest Editor Peter J. Chandler, 606B Berryfield Lane, Melksham, Wilts SN12 6EL (E-mail: [email protected]) Editorial Panel Graham Rotheray Keith Snow Alan Stubbs Derek Whiteley Phil Withers Dipterists Digest is the journal of the Dipterists Forum . It is intended for amateur, semi- professional and professional field dipterists with interests in British and European flies. All notes and papers submitted to Dipterists Digest are refereed. Articles and notes for publication should be sent to the Editor at the above address, and should be submitted with a current postal and/or e-mail address, which the author agrees will be published with their paper. Articles must not have been accepted for publication elsewhere and should be written in clear and concise English. Contributions should be supplied either as E-mail attachments or on CD in Word or compatible formats. The scope of Dipterists Digest is: - the behaviour, ecology and natural history of flies; - new and improved techniques (e.g. collecting, rearing etc.); - the conservation of flies; - reports from the Diptera Recording Schemes, including maps; - records and assessments of rare or scarce species and those new to regions, countries etc.; - local faunal accounts and field meeting results, especially if accompanied by ecological or natural history interpretation; - descriptions of species new to science; - notes on identification and deletions or amendments to standard key works and checklists.
    [Show full text]
  • Ohara\Catalogues\World Genera\Tach
    WORLD GENERA OF THE TACHINIDAE (DIPTERA) AND THEIR REGIONAL OCCURRENCE by James E. O’Hara1 23 February 2005 Version 1.0 ________________________ 1 Invertebrate Biodiversity, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario, Canada, K1A 0C6. E-mail: [email protected]. TABLE OF CONTENTS Click on a page number to go to the page indicated Foreword ............................................................................................................................... 2 Biogeographic summary ....................................................................................................... 3 Acknowledgements ............................................................................................................... 3 Table of genera and their regional occurrence ...................................................................... 4 References ........................................................................................................................... 66 Select a letter to go directly to corresponding genus in list of world genera A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z FOREWORD The following table is a listing of the tachinid genera of the world with their regional occurrence. It was compiled from the generic names and distributions given in the most recent regional catalogues, as listed here, and brought up-to-date using information from subsequently published papers. Regional catalogues Nearctic Region O’Hara & Wood (2004) Neotropical
    [Show full text]
  • Dipterists Forum
    BULLETIN OF THE Dipterists Forum Bulletin No. 76 Autumn 2013 Affiliated to the British Entomological and Natural History Society Bulletin No. 76 Autumn 2013 ISSN 1358-5029 Editorial panel Bulletin Editor Darwyn Sumner Assistant Editor Judy Webb Dipterists Forum Officers Chairman Martin Drake Vice Chairman Stuart Ball Secretary John Kramer Meetings Treasurer Howard Bentley Please use the Booking Form included in this Bulletin or downloaded from our Membership Sec. John Showers website Field Meetings Sec. Roger Morris Field Meetings Indoor Meetings Sec. Duncan Sivell Roger Morris 7 Vine Street, Stamford, Lincolnshire PE9 1QE Publicity Officer Erica McAlister [email protected] Conservation Officer Rob Wolton Workshops & Indoor Meetings Organiser Duncan Sivell Ordinary Members Natural History Museum, Cromwell Road, London, SW7 5BD [email protected] Chris Spilling, Malcolm Smart, Mick Parker Nathan Medd, John Ismay, vacancy Bulletin contributions Unelected Members Please refer to guide notes in this Bulletin for details of how to contribute and send your material to both of the following: Dipterists Digest Editor Peter Chandler Dipterists Bulletin Editor Darwyn Sumner Secretary 122, Link Road, Anstey, Charnwood, Leicestershire LE7 7BX. John Kramer Tel. 0116 212 5075 31 Ash Tree Road, Oadby, Leicester, Leicestershire, LE2 5TE. [email protected] [email protected] Assistant Editor Treasurer Judy Webb Howard Bentley 2 Dorchester Court, Blenheim Road, Kidlington, Oxon. OX5 2JT. 37, Biddenden Close, Bearsted, Maidstone, Kent. ME15 8JP Tel. 01865 377487 Tel. 01622 739452 [email protected] [email protected] Conservation Dipterists Digest contributions Robert Wolton Locks Park Farm, Hatherleigh, Oakhampton, Devon EX20 3LZ Dipterists Digest Editor Tel.
    [Show full text]
  • Millichope Park and Estate Invertebrate Survey 2020
    Millichope Park and Estate Invertebrate survey 2020 (Coleoptera, Diptera and Aculeate Hymenoptera) Nigel Jones & Dr. Caroline Uff Shropshire Entomology Services CONTENTS Summary 3 Introduction ……………………………………………………….. 3 Methodology …………………………………………………….. 4 Results ………………………………………………………………. 5 Coleoptera – Beeetles 5 Method ……………………………………………………………. 6 Results ……………………………………………………………. 6 Analysis of saproxylic Coleoptera ……………………. 7 Conclusion ………………………………………………………. 8 Diptera and aculeate Hymenoptera – true flies, bees, wasps ants 8 Diptera 8 Method …………………………………………………………… 9 Results ……………………………………………………………. 9 Aculeate Hymenoptera 9 Method …………………………………………………………… 9 Results …………………………………………………………….. 9 Analysis of Diptera and aculeate Hymenoptera … 10 Conclusion Diptera and aculeate Hymenoptera .. 11 Other species ……………………………………………………. 12 Wetland fauna ………………………………………………….. 12 Table 2 Key Coleoptera species ………………………… 13 Table 3 Key Diptera species ……………………………… 18 Table 4 Key aculeate Hymenoptera species ……… 21 Bibliography and references 22 Appendix 1 Conservation designations …………….. 24 Appendix 2 ………………………………………………………… 25 2 SUMMARY During 2020, 811 invertebrate species (mainly beetles, true-flies, bees, wasps and ants) were recorded from Millichope Park and a small area of adjoining arable estate. The park’s saproxylic beetle fauna, associated with dead wood and veteran trees, can be considered as nationally important. True flies associated with decaying wood add further significant species to the site’s saproxylic fauna. There is also a strong
    [Show full text]
  • Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016
    Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016 April 1981 Revised, May 1982 2nd revision, April 1983 3rd revision, December 1999 4th revision, May 2011 Prepared for U.S. Department of Commerce Ohio Department of Natural Resources National Oceanic and Atmospheric Administration Division of Wildlife Office of Ocean and Coastal Resource Management 2045 Morse Road, Bldg. G Estuarine Reserves Division Columbus, Ohio 1305 East West Highway 43229-6693 Silver Spring, MD 20910 This management plan has been developed in accordance with NOAA regulations, including all provisions for public involvement. It is consistent with the congressional intent of Section 315 of the Coastal Zone Management Act of 1972, as amended, and the provisions of the Ohio Coastal Management Program. OWC NERR Management Plan, 2011 - 2016 Acknowledgements This management plan was prepared by the staff and Advisory Council of the Old Woman Creek National Estuarine Research Reserve (OWC NERR), in collaboration with the Ohio Department of Natural Resources-Division of Wildlife. Participants in the planning process included: Manager, Frank Lopez; Research Coordinator, Dr. David Klarer; Coastal Training Program Coordinator, Heather Elmer; Education Coordinator, Ann Keefe; Education Specialist Phoebe Van Zoest; and Office Assistant, Gloria Pasterak. Other Reserve staff including Dick Boyer and Marje Bernhardt contributed their expertise to numerous planning meetings. The Reserve is grateful for the input and recommendations provided by members of the Old Woman Creek NERR Advisory Council. The Reserve is appreciative of the review, guidance, and council of Division of Wildlife Executive Administrator Dave Scott and the mapping expertise of Keith Lott and the late Steve Barry.
    [Show full text]
  • Chloropidae (Diptera) of Turkey with Descriptions of New Species and New Records
    ISRAEL JOURNAL OF ENTOMOLOGY, Vol. 41–42, 2011–2012, pp. 115–144 Chloropidae (Diptera) of Turkey with descriptions of new species and new records EMILIA P. NARTSHUK Zoological Institute of the Russian Academy of Sciences, Universitetskaya nab 1, 199034 St. Petersburg. E-mail: [email protected] ABSTRACT A list of Chloropidae from Turkey is provided, containing 64 species from 31 genera and 4 subfamilies. Three species are described as new. Two additional species were only identified to genus level. Twelve species are listed based only on literature data. Most species (40) are recorded from Turkey for the first time. KEYWORDS: Diptera, Chloropidae, Asia Minor, Turkey, new species, new faunistic data INTRODUCTION Grass flies of the family Chloropidae (Diptera, Cyclorrhapha) of Turkey are insuf- ficiently studied, and only 21 species have been recorded to date. Loew (1858) de- scribed 3 species: Oscinis brevirostris (now Aphanotrigonum cinctellum (Zetterstedt)), O. marginata (now Polyodaspis ruficornis (Macquart)) and Crassiseta megaspis (now in Elachiptera). He also cited Constantinopolis as type locality for the two former spe- cies and Asia minor for the latter species. Becker (1912) described Chlorops pallidior from Asia Minor. Duda (1932-1933) recorded Oscinimorpha albisetosa Duda, Chlo- rops fasciatus Meigen and Thaumatomyia sulcifrons Becker from Asia minor, Lodos (1957) recorded Oscinella frit (Linnaeus) as Scatopse nigra, but his drawings of the fly, including its wing, beyond question refer to O. frit. This species was mentioned by Özer (1976) as well. Lessman (1962), who studied pests of cones of Ceder libani, found larvae of a fly, which he did not name (see comments below under Hapleginella laevi- frons (Loew, 1858)).
    [Show full text]
  • The Evolutionary Life History of P Transposons: from Horizontal Invaders to Domesticated Neogenes
    Chromosoma (2001) 110:148–158 DOI 10.1007/s004120100144 CHROMOSOMA FOCUS Wilhelm Pinsker · Elisabeth Haring Sylvia Hagemann · Wolfgang J. Miller The evolutionary life history of P transposons: from horizontal invaders to domesticated neogenes Received: 5 February 2001 / In revised form: 15 March 2001 / Accepted: 15 March 2001 / Published online: 3 May 2001 © Springer-Verlag 2001 Abstract P elements, a family of DNA transposons, are uct of their self-propagating lifestyle. One of the most known as aggressive intruders into the hitherto uninfected intensively studied examples is the P element of Dro- gene pool of Drosophila melanogaster. Invading through sophila, a family of DNA transposons that has proved horizontal transmission from an external source they useful not only as a genetic tool (e.g., transposon tag- managed to spread rapidly through natural populations ging, germline transformation vector), but also as a model within a few decades. Owing to their propensity for rapid system for investigating general features of the evolu- propagation within genomes as well as within popula- tionary behavior of mobile DNA (Kidwell 1994). P ele- tions, they are considered as the classic example of self- ments were first discovered as the causative agent of hy- ish DNA, causing havoc in a genomic environment per- brid dysgenesis in Drosophila melanogaster (Kidwell et missive for transpositional activity. Tracing the fate of P al. 1977) and were later characterized as a family of transposons on an evolutionary scale we describe differ- DNA transposons
    [Show full text]
  • A Review of the Status of Larger Brachycera Flies of Great Britain
    Natural England Commissioned Report NECR192 A review of the status of Larger Brachycera flies of Great Britain Acroceridae, Asilidae, Athericidae Bombyliidae, Rhagionidae, Scenopinidae, Stratiomyidae, Tabanidae, Therevidae, Xylomyidae. Species Status No.29 First published 30th August 2017 www.gov.uk/natural -england Foreword Natural England commission a range of reports from external contractors to provide evidence and advice to assist us in delivering our duties. The views in this report are those of the authors and do not necessarily represent those of Natural England. Background Making good decisions to conserve species This report should be cited as: should primarily be based upon an objective process of determining the degree of threat to DRAKE, C.M. 2017. A review of the status of the survival of a species. The recognised Larger Brachycera flies of Great Britain - international approach to undertaking this is by Species Status No.29. Natural England assigning the species to one of the IUCN threat Commissioned Reports, Number192. categories. This report was commissioned to update the threat status of Larger Brachycera flies last undertaken in 1991, using a more modern IUCN methodology for assessing threat. Reviews for other invertebrate groups will follow. Natural England Project Manager - David Heaver, Senior Invertebrate Specialist [email protected] Contractor - C.M Drake Keywords - Larger Brachycera flies, invertebrates, red list, IUCN, status reviews, IUCN threat categories, GB rarity status Further information This report can be downloaded from the Natural England website: www.gov.uk/government/organisations/natural-england. For information on Natural England publications contact the Natural England Enquiry Service on 0300 060 3900 or e-mail [email protected].
    [Show full text]
  • Of the Vitosha Mountain
    Historia naturalis bulgarica 26: 1–66 ISSN 0205-3640 (print) | ISSN 2603-3186 (online) • http://www.nmnhs.com/historia-naturalis-bulgarica/ publication date [online]: 17 May 2018 The Dipterans (Insecta: Diptera) of the Vitosha Mountain Zdravko Hubenov Abstract. A total of 1272 two-winged species that belong to 58 families has been reported from theVitosha Mt. The Tachinidae (208 species or 16.3%) and Cecidomyiidae (138 species or 10.8%) are the most numerous. The greatest number of species has been found in the mesophylic and xeromesophylic mixed forests belt (707 species or 55.6%) and in the northern part of the mountain (645 species or 50.7%). The established species belong to 83 areographical categories. The dipterous fauna can be divided into two main groups: 1) species with Mediterranean type of distribution (53 species or 4.2%) – more thermophilic and distributed mainly in the southern parts of the Palaearctic; seven species of southern type, distributed in the Palaearctic and beyond it, can be formally related to this group as well; 2) species with Palaearctic and Eurosiberian type of distribution (1219 species or 95.8%) – more cold-resistant and widely distributed in the Palaearctic; 247 species of northern type, distributed in the Palaearctic and beyond it, can be formally related to this group as well. The endemic species are 15 (1.2%). The distribution of the species according to the zoogeographical categories in the vegetation belts and the distribution of the zoogeographical categories in each belt are considered. The dipteran fauna of the Vitosha Mt. is compared to this of the Rila and Pirin Mountains.
    [Show full text]
  • Diptera) of the Czech Republic
    © Entomologica Fennica. 30 March 2009 Annotated host catalogue for the Tachinidae (Diptera) of the Czech Republic Jaromir Vafihara*, Hans-Peter Tschorsnig, Benno Herting’r, Petr Mfickstein & Veronika Michalkova J P. & V. Vanhara, ., Tschorsnig, H.-P., Herting, B., Miickstein, Michalkova, 2009: Annotated host catalogue for the Tachinidae (Diptera) of the Czech Re- public. — Entomol. Fennica 20: 22—48. An annotated host catalogue is given for the Tachinidae ofthe Czech Republic. It comprises 149 of476 tachinid species which are currently known from this coun- try (included the two new records cited below). 195 hosts are listed. The first host records ofTachinidae date back to the second halfofthe 19th century. The bibli- ography for the host records consists of 1 16 papers of 55 researchers. Several re- cords of hitherto unpublished material are included. Phryxe setifacies and Anthomyiopsis plagioderae are first records for the Czech Republic. J. Vanhara (*corresponding author), Masaryk University, Faculty ofScience, Kotlarska 2, CZ—6I I 3 7 Brno, Czech Republic, [email protected] H.—P. Tschorsnig, Staatliches Museumflir Naturkunde, Rosenstein I, D— 70 191 Stuttgart, Germany, tschorsnig.smns@naturkundemuseum—bw.de P. Muckstein Administration of the Protected Landscape Area Zd’drske' vrchy, Brnenska 39, CZ—591 01 Zd’dr nad Sazavou, Czech Republic, muchstein @email.cz V. Michalkova, Masaryk University, Faculty ofScience, Kotlarska 2, CZ—6I I 3 7 Brno, Czech Republic, [email protected] Received 22 August 200 7, accepted 21 January 2008 1. Introduction The tachinid species are listed in their actual valid nomenclature; probable misidentifications Tachinidae are a very large and important dipter- are — if possible — tentatively corrected, but the an family of (mainly) insect parasitoids.
    [Show full text]
  • Notable Species Associated with Lowland Wood Pasture
    Notable species associated with lowland wood pasture Spiders and allies (Arachnida: Araneae and Pseudoscorpiones) Mastigusa arietina RDB2 Mastigusa macrophthalma RDB3 Midia midas RDB2 Pistius truncatus RDB1 Tuberta maerens RDB3 Achaearanea simulans Nb Clubiona caerulescens Nb Haplodrassus silvestris Nb Marpissa muscosa Nb Meta bourneti Nb Philodromus albidus Nb Philodromus margaritatus Nb Philodromus praedatus Nb Salticus zebraneus Na Xysticus luctuosus Nb Zygiella stroemi Nb Pseudoscorpiones Dendrochernes cyrneus RDB3 Centipedes (Chilopoda) Chalandea pinguis Nb Lithobius muticus Nb Woodlice (Isopoda) Trichoniscoides helveticus Nb Grasshoppers, crickets, earwigs & cockroaches (Orthoptera/Dermaptera/Dictyoptera) Nemobius sylvestris Na Omocestus rufipes Nb Ectobius lapponicus Nb True bugsHemiptera Heteroptera Aradus aterrimus RDB3 Aradus corticalis RDB3 Lygus pratensis RDB3 Sehirus biguttatus Nb Eurydema dominulus Na Oncochila simplex Nb Empicoris baerunspringi Na Myrmedobia coleoptrata Nb Psallus albicinctus Nb Aradus depressus Local Reduvius personatus Local Leafhoppers, planthoppers, froghoppers, treehoppers & cicadas (Auchenorrhyncha) Pediopsis tiliae Nb Flies (Diptera) Snail-killing flies, picture-wing flies, grass flies and allies (Acalyptrata) Amiota variegata (Drosophilidae) RDB1 Astiosoma rufifrons (Asteiidae) RDB2 Gaurax britannicus (Chloropidae) RDBK Madiza pachymera (Milichiidae) RDB3 Myennis octopunctata (Ulidiidae) RDB2 Paraclusia tigrina (Clusiidae) RDB2 Periscelis winnertzi (Periscelididae) RDB1 Odinia maculata (Odiniidae)
    [Show full text]
  • Diptera) of Finland 311 Doi: 10.3897/Zookeys.441.7505 CHECKLIST Launched to Accelerate Biodiversity Research
    A peer-reviewed open-access journal ZooKeys 441: 311–318 (2014)Checklist of the family Chloropidae (Diptera) of Finland 311 doi: 10.3897/zookeys.441.7505 CHECKLIST www.zookeys.org Launched to accelerate biodiversity research Checklist of the family Chloropidae (Diptera) of Finland Emilia Nartshuk1, Jere Kahanpää2 1 Zoological Institute of the Russian Academy of Sciences, Universitetskaya nab. 1 St.-Petersburg 199034 Russia 2 Finnish Museum of Natural History, Zoology Unit, P.O. Box 17, FI-00014 University of Helsinki, Finland Corresponding author: Emilia Nartshuk ([email protected]) Academic editor: J. Salmela | Received 24 March 2014 | Accepted 10 June 2014 | Published 19 September 2014 http://zoobank.org/782B4E3D-E88F-46E7-BB77-1A51666A4DD5 Citation: Nartshuk E, Kahanpää J (2014) Checklist of the family Chloropidae (Diptera) of Finland. In: Kahanpää J, Salmela J (Eds) Checklist of the Diptera of Finland. ZooKeys 441: 311–318. doi: 10.3897/zookeys.441.7505 Abstract A checklist of 147 species the Chloropidae (Diptera) recorded from Finland. Centorisoma elegantulum Becker is recorded for the first time from Finland. Keywords Finland, Chloropidae, species list, biodiversity, faunistics Introduction The Chloropidae is a large family of acalyptrate Diptera. It belongs to superfamily Carnoidea with Milichiidae as the closest relative. The classification of the family used follows Andersson (1977) and Nartshuk (1983). The North European chloropid fauna has recently been revised by Nartshuk and Andersson (2013). Details of Finnish chloropid literature, species distribution and ecology, and other details can be found in their book. In comparison with the neigh- bouring countries, Finland ranks second in the number of chloropid species after Swe- den (189 species) but well ahead of Denmark (119 species) and Norway (97 species).
    [Show full text]