INSECTS of MICRONESIA Diptera: Coelopidae (Phycodromidaey
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Life Cycle and Kelp Consumption of Paractora Dreuxi Mirabilis (Diptera: Helcomyzidae): a Primary Decomposer of Stranded Kelp on Marion Island
18 S. Afr. T. Nav. Antarkt., Deel 14, 1984 1 Life cycle and kelp consumption of Paractora dreuxi mirabilis (Diptera: Helcomyzidae): A primary decomposer of stranded kelp on Marion Island J.E. Crafford Department of Entomology University of Pretoria, Hatfield , Pretoria 0083 Wrack beds of the intertidal kelp Durvillea antarctica (Cham.) Apetenus liroralis and Paractora dreuxi mirabilis. are closely Har. on Marion Island (46°54' S, 37"45' E) sustain large kelp fly associated with wrack beds and decomposing kelp. populatior.s. Paractora dreuxi mirabilis (Seguy) is a primary Little is known about the nutrient and energy pathways decomposer of stranded Durv11lea with larvae reaching a operative in the littoral zone on Marion Island (Smith 1977). biomass of2 gper kg ofdecomposing kelp (wet mass). At 10°C Fronds of Durvillea antarccica, an epilitic phaeophyte Paractora completes its life cycle in 80-120 days. Egg, larval and abounding in the intertidal zone, continuously wash up on pupal stages last 4, 60 and 40 days respectively. Larvae eat 0,5 beaches around the island. After heavy seas fronds frequently rimes their own dry mass in kelp per day. They attain an indivi pile up into large and dense wrack beds. Paractora larvae are dual live mass of up to JOO mg. The feeding and burrowing the major decomposers of beached Durvillea, representing by activity of larvae probably enhance microbial decay ofbeached far the greatest biomass of decomposers in beached kelp kelp. Paractora larvae are preyed on by vertebrate insectivores (Crafford, unpublished) and constituting an easily explo1table and probably form an important link in nutrient and energy localised food resource for secondary consumers such as the chains in the littoral zone on Marion Island. -
Superfamilies Tephritoidea and Sciomyzoidea (Dip- Tera: Brachycera) Kaj Winqvist & Jere Kahanpää
20 © Sahlbergia Vol. 12: 20–32, 2007 Checklist of Finnish flies: superfamilies Tephritoidea and Sciomyzoidea (Dip- tera: Brachycera) Kaj Winqvist & Jere Kahanpää Winqvist, K. & Kahanpää, J. 2007: Checklist of Finnish flies: superfamilies Tephritoidea and Sciomyzoidea (Diptera: Brachycera). — Sahlbergia 12:20-32, Helsinki, Finland, ISSN 1237-3273. Another part of the updated checklist of Finnish flies is presented. This part covers the families Lonchaeidae, Pallopteridae, Piophilidae, Platystomatidae, Tephritidae, Ulididae, Coelopidae, Dryomyzidae, Heterocheilidae, Phaeomyii- dae, Sciomyzidae and Sepsidae. Eight species are recorded from Finland for the first time. The following ten species have been erroneously reported from Finland and are here deleted from the Finnish checklist: Chaetolonchaea das- yops (Meigen, 1826), Earomyia crystallophila (Becker, 1895), Lonchaea hirti- ceps Zetterstedt, 1837, Lonchaea laticornis Meigen, 1826, Prochyliza lundbecki (Duda, 1924), Campiglossa achyrophori (Loew, 1869), Campiglossa irrorata (Fallén, 1814), Campiglossa tessellata (Loew, 1844), Dioxyna sororcula (Wie- demann, 1830) and Tephritis nigricauda (Loew, 1856). The Finnish records of Lonchaeidae: Lonchaea bruggeri Morge, Lonchaea contigua Collin, Lonchaea difficilis Hackman and Piophilidae: Allopiophila dudai (Frey) are considered dubious. The total number of species of Tephritoidea and Sciomyzoidea found from Finland is now 262. Kaj Winqvist, Zoological Museum, University of Turku, FI-20014 Turku, Finland. Email: [email protected] Jere Kahanpää, Finnish Environment Institute, P.O. Box 140, FI-00251 Helsinki, Finland. Email: kahanpaa@iki.fi Introduction new millennium there was no concentrated The last complete checklist of Finnish Dipte- Finnish effort to study just these particular ra was published in Hackman (1980a, 1980b). groups. Consequently, before our work the Recent checklists of Finnish species have level of knowledge on Finnish fauna in these been published for ‘lower Brachycera’ i.e. -
1659 2012-10323.Pdf
Zootaxa 3478: 553–569 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2012 · Magnolia Press Article ISSN 1175-5334 (online edition) urn:lsid:zoobank.org:pub:EC0F0A87-8BF4-42C6-8561-0AC2ED45E00F The new genus Acrocephalomyia, and a new species of Ropalomera from Costa Rica, with additional records for other Mesoamerican species (Diptera: Ropalomeridae) SERGIO IBÁÑEZ-BERNAL 1 & VICENTE HERNÁNDEZ-ORTIZ 2 1Red Ambiente y Sustentabilidad, Instituto de Ecología, A.C. Carretera antigua a Coatepec No. 351, El Haya, Xalapa, 91070, Veracruz, México. E–mail: [email protected] 2Red Interacciones Multitróficas, Instituto de Ecología, A.C. Carretera antigua a Coatepec No. 351, El Haya, Xalapa, 91070, Veracruz, México. E–mail: [email protected] Abstract New taxa of the family Ropalomeridae from Costa Rica are described, and additional records of ropalomerid flies from Mexico and Central America are provided. The new genus and species Acrocephalomyia zumbadoi can be easily distin- guished from all other ropalomerid genera by the following combination of characters: angular forward projection of head, absence of ocelli, flat face, bare arista, long scutum, and scutellum triangular-shaped and dorsally flattened with only one pair of apical bristles with bases approximated. The new species Ropalomera aterrima can be recognized from congeners by remarkable differences of the head, the shape of the scutellum, the absence of scutal vittae, fumose wings, and by the black coloration of the body, ocellar bristles large, one postpronotal bristle, scutum without pollinose vittae and flat scutel- lum. Lenkokroeberia chryserea Prado and Kroeberia fuliginosa Lindner are newly confirmed for Costa Rica. -
Genetic Divergence and Phenotypic Plasticity Contribute to Variation in Cuticular Hydrocarbons in the Seaweed Fly Coelopa Frigida
Received: 23 June 2019 | Revised: 19 August 2019 | Accepted: 26 August 2019 DOI: 10.1002/ece3.5690 ORIGINAL RESEARCH Genetic divergence and phenotypic plasticity contribute to variation in cuticular hydrocarbons in the seaweed fly Coelopa frigida Emma Berdan1 | Swantje Enge2,3 | Göran M. Nylund3 | Maren Wellenreuther4,5 | Gerrit A. Martens6 | Henrik Pavia3 1Department of Marine Sciences, University of Gothenburg, Göteborg, Sweden Abstract 2Institute for Chemistry and Biology of the Cuticular hydrocarbons (CHCs) form the boundary between insects and their envi‐ Marine Environment, Carl‐von‐Ossietzky ronments and often act as essential cues for species, mate, and kin recognition. This University Oldenburg, Wilhelmshaven, Germany complex polygenic trait can be highly variable both among and within species, but 3Department of Marine Sciences – the causes of this variation, especially the genetic basis, are largely unknown. In this Tjärnö, University of Gothenburg, Strömstad, Sweden study, we investigated phenotypic and genetic variation of CHCs in the seaweed fly, 4Plant & Food Research Limited, Nelson, Coelopa frigida, and found that composition was affected by both genetic (sex and New Zealand population) and environmental (larval diet) factors. We subsequently conducted be‐ 5School of Biological Sciences, The havioral trials that show CHCs are likely used as a sexual signal. We identified general University of Auckland, Auckland, New Zealand shifts in CHC chemistry as well as individual compounds and found that the meth‐ 6 Institute for Zoology, University of ylated compounds, mean chain length, proportion of alkenes, and normalized total Hamburg, Hamburg, Germany CHCs differed between sexes and populations. We combined these data with whole Correspondence genome resequencing data to examine the genetic underpinnings of these differ‐ Emma Berdan, Department of Marine Sciences, University of Gothenburg, Box ences. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
UC Santa Barbara Posters
UC Santa Barbara Posters Title From rejection to collection! A new entomology collection at the University of California, Santa Barbara Museum of Natural History takes the university by swarm. Permalink https://escholarship.org/uc/item/90j9s4jh Authors Behm, Rachel Seltmann, Katja, PhD Publication Date 2017 License https://creativecommons.org/licenses/by-sa/4.0/ 4.0 eScholarship.org Powered by the California Digital Library University of California From rejection to collection! A new entomology collection at the University of California, Santa Barbara Museum of Natural History takes the university by swarm. Rachel Behm & Katja C. Seltmann Cheadle Center for Biodiversity and Ecological Restoration, Harder South Building 578, Santa Barbara, CA 93106 Introduction Results The University of California, Santa Barbara (UCSB) Natural History Museum at the Cheadle Center As of October 2017, the database has a total of 1,432 specimens. We are georeferencing the Where the U.S. Diptera Specimens Came From for Biodiversity and Ecological Restoration (CCBER) has formed an Invertebrate Zoology Collection specimens, with almost 900 completed (Table 1). Databasing of the Diptera is complete and our 0.15% 0.15% 0.15% Arizona from 10,000 specimens rediscovered in a basement on campus. Since its discovery, this collection entire Diptera collection of currently 715 specimens (35 families and 33 genera) has been 6.02% 3.82% has grown rapidly through coastal California arthropod survey efforts, donated student collections, transcribed and georeferenced. Determination to family for the Acalyptratae is ongoing. Currently California and faculty research projects (Fig. 2). These surveys, conducted by CCBER for conservation and in the SCAN data portal there are 326 Diptera specimens (14 families and 24 genera) from coastal Michigan restoration monitoring, are hugely valuable as the coastal regions of Santa Barbara and Ventura Santa Barbara and Ventura counties. -
The Hessian Fly in California
". ~. .: "" ~ .- - - " .... ,' ~ .-,. '-' .. :'.~'~' ;::-" - ~ '"' - "'= -, ..... ~~~ ~-~ ',' I~ 111112.~ 2 5 I~ 2 5 W 1= 11111 . 1I11~ 11111 . 1.0 3 2 w W 1 . W ~3.2 .2 II ~ ~ t.:.: Ii.£ t.:.: w w I~ I:: I:: '" ~ ... I~ 1.1 '"..;a~~ " 1.1 I..a.:.""0.::. " - 111111.25 111111.4 111111.6 111111.25 111111.4 111111.6 MICROCOPY RESOLUTION TEST CHART MICROCOPY RESOLUTION TEST \Alh~T NATIONAL BUREAU Of STANOARDS-1963-A NATIONAL BUREAU Of STANDARDS-1963-A . )"' :~);. UNiTED'ST{1TESi)E~~~~ 9F;AG~CUL~' . WASHINGTON, D. C. ' .... ~THE HESsiAN FLY I~ ·CALIFQR.NIA!), .;~4 ,." e ~ ~ 7~,' ; ~ " } uy C. M. PACJtAJili; 'Seni6r'iiintomQlogist, D£",iiWn of Om-eta and-Forage 1ft86'*s,. 1 <.;:t"" ' ,Bureau of EntOfniJpJw " ; ." . coNTENTs ' Page' PIige Ee6nomfe fmportSnce..,.. .._,..,._.; _____ '-, t Met~~!oglcal"Summer mortalitY' control~Contbiued. __________ _ History________---"-"-..:-------..:..--- 3 Artificial 16 Seasonal lilstory________________.. 4 controL____ .:_.;·________ _ -l7 Character of Injury______________ 7 Burning. stubble _______-' ____ _ 17 Development _____________________ 10 Burying stubble by plowlug ___ _ 17 Summer' cultivation 'of stubble":_ 18 " ~~: l:~k:::::=::=:::::::::::::::::::::::: J~ Spraying stubble to.kill pUI!tlrlll- 19 Early plantlng_______________ _ 20 . ~~: f~::::::::::::::::::::::::::::::::=:::: ' . ~ Rotation of crops ____________ _ 20 SummaryPlanting._____________________ resistant. varletles_____ . 20 ~~~sft~~n~~_~_~'_~:r..<>~~~::::::::::=:::::: U Literature cited _____.. _____ .:.____ _ 24 Meteorological controL____________ 15 2:; . Early spring mortality_______ 15 c ':J .' ECONOl\IIC IMPORTANCE In Californin, the H~~ian fly (PhytopMga' dest'MtCtor Say) is of economic' importance O)~Y in wheat.,growing regions near ti,.e coast, where the influence oi' :the ocean is .sufficient to prevent eXtremely high" summer temperatu~es. -
On Adult Size and Male Mating Success in the Seaweed Fly, Coelopa Frigida A
Heredity (1982), 49 (1),51—62 0018-067X/82/0507005 1$02.OO 1982.The Genetical Society of Great Britain THEEFFECTS OF A CHROMOSOMAL INVERSION ON ADULT SIZE AND MALE MATING SUCCESS IN THE SEAWEED FLY, COELOPA FRIGIDA A. K. BUTLIN, I. L. READ and 1. H. DAY Department of Genetics, University of Nottingham, University Park, Nottingham, NG72RD Received4.iii.82 SUMMARY An association is reported between the a//3inversionpolymorphism on chromo- some I and adult size as assessed by the length of wings. aa flies are larger than (3/3 flies, with heterokaryotypes intermediate, and the differences are more marked in males than in females. Laboratory mating experiments were perfor- med in which a single female was given a choice of two males. By examining the genotypes of the progeny larvae, it is shown that the larger male is successful in a significantly greater proportion of trials than the smaller one. This mating success is dependent on the size difference between the males and on the female size. Together these observations suggest an indirect influence of the inversion on male mating success. The possible relevance of this effect to the maintenance of the inversion polymorphism in natural populations is discussed. 1. INTRODUCTION MANY species of insects are polymorphic for chromosomal inversions. The most extensive studies of these polymorphisms have been in various species of Drosophila (da Cunha, 1955) especially D.pseudoobscura(Dobzhansky, 1971), D. persimilis (Spiess and Spiess, 1969; Yu and Spiess, 1978) and D. subobscura (Krimbas and Loukas, 1979). It is clear from the Drosophila work that there exists a multitude of selection pressures that may influence the frequencies of inversions in natural populations. -
Advances in Deciphering the Genetic Basis of Insect Cuticular Hydrocarbon Biosynthesis and Variation
Heredity (2021) 126:219–234 https://doi.org/10.1038/s41437-020-00380-y REVIEW ARTICLE Advances in deciphering the genetic basis of insect cuticular hydrocarbon biosynthesis and variation 1 1 1,2 Henrietta Holze ● Lukas Schrader ● Jan Buellesbach Received: 6 July 2020 / Revised: 8 October 2020 / Accepted: 9 October 2020 / Published online: 2 November 2020 © The Author(s) 2020. This article is published with open access Abstract Cuticular hydrocarbons (CHCs) have two fundamental functions in insects. They protect terrestrial insects against desiccation and serve as signaling molecules in a wide variety of chemical communication systems. It has been hypothesized that these pivotal dual traits for adaptation to both desiccation and signaling have contributed to the considerable evolutionary success of insects. CHCs have been extensively studied concerning their variation, behavioral impact, physiological properties, and chemical compositions. However, our understanding of the genetic underpinnings of CHC biosynthesis has remained limited and mostly biased towards one particular model organism (Drosophila). This rather narrow focus has hampered the establishment of a comprehensive view of CHC genetics across wider phylogenetic 1234567890();,: 1234567890();,: boundaries. This review attempts to integrate new insights and recent knowledge gained in the genetics of CHC biosynthesis, which is just beginning to incorporate work on more insect taxa beyond Drosophila. It is intended to provide a stepping stone towards a wider and more general understanding of the genetic mechanisms that gave rise to the astonishing diversity of CHC compounds across different insect taxa. Further research in this field is encouraged to aim at better discriminating conserved versus taxon-specific genetic elements underlying CHC variation. -
Coleoptera: Staphylinidae: Genus Aleochara) from Japan
Zootaxa 3517: 1–52 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2012 · Magnolia Press Article ISSN 1175-5334 (online edition) urn:lsid:zoobank.org:pub:F832C768-A8CA-4FEE-8C3B-BD933247FA6E Revision of the Seashore-dwelling Subgenera Emplenota Casey and Triochara Bernhauer (Coleoptera: Staphylinidae: genus Aleochara) from Japan SHÛHEI YAMAMOTO1, 2 & MUNETOSHI MARUYAMA2, 3 1Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Hakozaki 6-10-1, Fukuoka, 812-8581 Japan E-mail: [email protected] 2The Kyushu University Museum, Hakozaki 6-10-1, Fukuoka, 812-8581 Japan 3Correspoding author: E-mail: [email protected] Abstract The Japanese species of the seashore-dwelling subgenera Emplenota Casey and Triochara Bernhauer of the genus Aleochara Gravenhorst are revised. Five species are recognised in Emplenota, of which three are described as new species: Aleochara (Emplenota) segregata n. sp., A. (E.) hayamai n. sp. and A. (E.) yamato n. sp. The remaining known species A. (E.) fucicola Sharp and A. (E.) puetzi (Assing) are redescribed. Three species recognised in Triochara, Aleochara (Triochara) trisulcata Weise, A. (T.) zerchei (Assing) and A. (T.) nubis (Assing) are redescribed. All species are keyed. For some species ecological data are reported. The phylogenetic relationships of the Japanese species are discussed, and the distributions of all species are mapped. Key words: biodiversity, coastal environment, identification key, Palaearctic, redescription, supratidal zones, sympatric species, taxonomy Introduction Recent studies have revealed the worldwide coastal staphylinid diversity (Moore & Legner, 1976; Hammond, 2000; Frank & Ahn, 2011), and the subfamily Aleocharinae is represented by 187 species throughout the world, representing the largest number of coastal staphylinid beetles (Frank & Ahn, 2011). -
Calyptratae: Diptera)
BUILDING THE TREE OF LIFE: RECONSTRUCTING THE EVOLUTION OF A RECENT AND MEGADIVERSE BRANCH (CALYPTRATAE: DIPTERA) SUJATHA NARAYANAN KUTTY (B.Tech) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARTMENT OF BIOLOGICAL SCIENCES NATIONAL UNIVERSITY OF SINGAPORE 2008 The great tragedy of Science - the slaying of a beautiful hypothesis by an ugly fact. - Thomas H. Huxley ii ACKNOWLEDGEMENTS We don't accomplish anything in this world alone... and whatever happens is the result of the whole tapestry of one's life and all the weavings of individual threads from one to another that creates something - Sandra Day O'Connor. The completion of this project would have been impossible without help from so many different quarters and the few lines of gratitude and acknowledgements written out in this section would do no justice to the actual amount of support and encouragement that I have received and that has contributed to making this study a successful endeavor. I am indebted to Prof. Meier for motivating me to embark on my PhD (at a very confusing point for me) and giving me a chance to explore a field that was quite novel to me. I express my sincere gratitude to him for all the guidance, timely advice, pep talks, and support through all the stages of this project and for always being patient while dealing with my ignorance. He has also been very understanding during all my non- academic distractions in the last two years. Thanks Prof.- your motivation and inspiration in the five years of my graduate study has given me the confidence to push the boundaries of my own capabilities. -
Behavioural, Ecological, and Genetic Determinants of Mating and Gene
Thesis committee Thesis supervisor Prof. dr. Marcel Dicke Professor of Entomology, Wageningen University Thesis co-supervisor Dr. Ir. Bart G.J. Knols Medical Entomologist, University of Amsterdam Other members Prof. dr. B.J. Zwaan, Wageningen University Prof. dr. P. Kager, University of Amsterdam Dr. Ir. P. Bijma, Wageningen University Dr. Ir. I.M.A. Heitkonig, Wageningen University This research was conducted under the auspices of the C. T. de Wit Graduate School for Production Ecology and Resource Conservation Behavioural, ecological and genetic determinants of mating and gene flow in African malaria mosquitoes Kija R.N. Ng’habi Thesis Submitted in fulfillment of the requirement for the degree of doctor at Wageningen University by the authority of the Rector Magnificus Prof. dr. M.J. Kropff, in the presence of the Thesis committee appointed by the Academic Board to be defended in public at on Monday 25 October 2010 at 11:00 a.m. in the Aula. Kija R.N. Ng’habi (2010) Behavioural, ecological and genetic determinants of mating and gene flow in African malaria mosquitoes PhD thesis, Wageningen University – with references – with summaries in Dutch and English ISBN – 978-90-8585-766-2 > Abstract Malaria is still a leading threat to the survival of young children and pregnant women, especially in the African region. The ongoing battle against malaria has been hampered by the emergence of drug and insecticide resistance amongst parasites and vectors, re- spectively. The Sterile Insect Technique (SIT) and genetically modified mosquitoes (GM) are new proposed vector control approaches. Successful implementation of these ap- proaches requires a better understanding of male mating biology of target mosquito species.