Insects and Other Arthropods from Laysan Island
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Dachtylembia, a New Genus in the Family Teratembiidae (Embioptera) from Thailand
Zootaxa 3779 (4): 456–462 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3779.4.3 http://zoobank.org/urn:lsid:zoobank.org:pub:84B1F99D-8F30-4B8C-9B3F-F25F750A5886 Dachtylembia, a new genus in the family Teratembiidae (Embioptera) from Thailand PISIT POOLPRASERT Faculty of Science and Technology, Pibulsongkram Rajabhat University, Phitsanulok, 65000, Thailand. E-mail: [email protected] Abstract Dachtylembia gen. nov. (Embioptera: Teratembiidae), is described and illustrated based on specimens of a new species (D. siamensis) collected from Thailand. The geographical distribution of this species in Thailand is mapped. Key words: Dachtylembia siamensis, new species, taxonomy Introduction The family Teratembiidae, a relatively small group of Embioptera, was established by Krauss (1911). Four genera in this family are currently listed (Szumik 1994; Miller 2009): Diradius Friederichs, 1934, Oligembia Davis, 1939, Paroligembia Ross, 1952 and Teratembia Krauss, 1911. Teratembiidae is considered a sister group of Oligotomidae (Szumik 1994; Szumik et al. 1996, 2008; Miller et al. 2012). This family is well represented in Nearctic, Neotropical and Afrotropical regions (Ross 1984, Miller 2009). Teratembiids can be recognized by several characteristics: the forked anterior media (AM) in the wing; hind leg with only one basitarsal papilla; hemitergites of the tenth segment (10L and 10R) fused to an extremely large medial sclerite (MS); epiproct (EP) and right tergal process of tenth segment (10 RP) completed separated from the right 10R; left cercus-basipodite (LCB) fused to the base of left cercus and bearing one or more small mesal lobes; first segment of left cercus (LC1) not echinulate. -
Article History Keywords Cantaloupe, Natural Enemies, Diptera
Egypt. J. Plant Prot. Res. Inst. (2020), 3 (2): 571 - 579 Egyptian Journal of Plant Protection Research Institute www.ejppri.eg.net Dipteran and coleopteran natural enemies associated with cantaloupe crop in Qalyubiya Governorate, Egypt El-Torkey, A.M. 1; Younes, M. W. F.², Mohi-Eldin, A. I. 1 and Abd Allah, Y.N.M. 1 1Plant Protection Research Institute, Agricultural Research Center, Dokki, Giza, Egypt. ²Zoology Department, Faculty of Science, Menofia University, Egypt. ARTICLE INFO Abstract: Article History Studying diversity of natural enemies associated with their pests Received: 21/ 4 /2020 in agro ecosystems is urgent for the integrated pest management. Two Accepted: 17 / 5 /2020 sampling techniques (i.e. water traps (pit-fall traps) and direct count of _______________ insects in the field) were used to survey pests, natural enemies and Keywords pollinators on six cantaloupe cultivars in Qaha region of Qalyubiya Cantaloupe, Governorate, Egypt over 2006 and 2007 summer plantation seasons. natural enemies, Thirty-two species belonging to two insects in Diptera and Coleoptera Diptera, orders presented by 18 superfamilies and 23 families and 22 genera. Coleoptera, They were recorded on Ideal, E81-065, Mirella, Vicar, E81-013 and Qalyubiya Magenta cantaloupe cultivars. Diptera was represented by eighteen Governorate and species belonging to 13 families (Sepsidae, Phoridae, Scenophilidae, Egypt. Dolichpodidae, Otitidae, Agromyzidae, Ephydridae, Drosophilidae, Tachinidae, Anthomyiidae, Muscidae, Syrohidae and Cecidomyiidae). Field observations indicated that Liriomyza trifolii (Burg), Agromyzidae infested cantaloupe leaves in moderate populations, while Melanogromyza cuntans (Meign) infested leaves in low populations. The present study revealed that the parasite Tachina larvarum L. (Tachinidae) and the predator Syrphus corolla F. -
Faune De Belgique 2
Faune de Belgique / Fauna van Belgi Bulletin de la Société royale belge d’Entomologie/Bulletin van de Koninklijke Belgische Vereniging voor Entomologie, 151 (2015): 195-197 Pteroxanium kelloggi (Ribaga, 1905) and Mesopsocus fuscifrons Meinander, 1966: two Psocoptera new to Belgium Koen LOCK 1, Henk WALLYS 2, Stéphane CLAEREBOUT 3 & Jan SOORS 4 1 Ghent University, Laboratory of Environmental Toxicology and Aquatic Ecology, J. Plateaustraat 22, B-9000 Ghent, Belgium (e-mail: [email protected]) 2 Ter Goedingen 40, B-9881 Bellem, Belgium 3 Centre Marie-Victorin, Centre de Recherche et d’Éducation pour la Conservation de la Nature, rue des Écoles 21, B-5670 Vierves-sur-Viroin, Belgium 4 Research Institute for Nature and Forest, Kliniekstraat 25, B-1070 Brussels, Belgium Abstract Two Psocoptera are reported here for the first time for the Belgian fauna. Pteroxanium kelloggi (Ribaga, 1905) is the first representative of the family Lepidopsocidae in Belgium and the species was observed in Bellem and Nismes. Mesopsocus fuscifrons Meinander, 1966 from the family Mesopsocidae was found in Antwerp and Mechelen. Keywords : barkfly, Lepidopsocidae, Mesopsocidae, Mesopsocus fuscifrons, Pteroxanium kelloggi . Samenvatting Twee stofluizen of Psocoptera worden hier voor het eerst gemeld voor de Belgische fauna. Pteroxanium kelloggi (Ribaga, 1905) is de eerste vertegenwoordiger van de familie Lepidopsocidae in België en de soort werd waargenomen in Bellem en Nismes. Mesopsocus fuscifrons Meinander, 1966 van de familie Mesopsocidae werd in Antwerpen en Mechelen gevonden. Résumé Deux Psocoptères sont rapportés ici pour la première fois pour la faune belge. Pteroxanium kelloggi (Ribaga, 1905) est le premier représentant de la famille des Lepidopsocidae pour le pays et l’espèce a été observée à Bellem et Nismes. -
Hastings Slide Collection3
HASTINGS NATURAL HISTORY RESERVATION SLIDE COLLECTION 1 ORDER FAMILY GENUS SPECIES SUBSPECIES AUTHOR DATE # SLIDES COMMENTS/CORRECTIONS Siphonaptera Ceratophyllidae Diamanus montanus Baker 1895 221 currently Oropsylla (Diamanus) montana Siphonaptera Ceratophyllidae Diamanus spp. 1 currently Oropsylla (Diamanus) spp. Siphonaptera Ceratophyllidae Foxella ignota acuta Stewart 1940 402 syn. of F. ignota franciscana (Roths.) Siphonaptera Ceratophyllidae Foxella ignota (Baker) 1895 2 Siphonaptera Ceratophyllidae Foxella spp. 15 Siphonaptera Ceratophyllidae Malaraeus spp. 1 Siphonaptera Ceratophyllidae Malaraeus telchinum Rothschild 1905 491 M. telchinus Siphonaptera Ceratophyllidae Monopsyllus fornacis Jordan 1937 57 currently Eumolpianus fornacis Siphonaptera Ceratophyllidae Monopsyllus wagneri (Baker) 1904 131 currently Aetheca wagneri Siphonaptera Ceratophyllidae Monopsyllus wagneri ophidius Jordan 1929 2 syn. of Aetheca wagneri Siphonaptera Ceratophyllidae Opisodasys nesiotus Augustson 1941 2 Siphonaptera Ceratophyllidae Orchopeas sexdentatus (Baker) 1904 134 Siphonaptera Ceratophyllidae Orchopeas sexdentatus nevadensis (Jordan) 1929 15 syn. of Orchopeas agilis (Baker) Siphonaptera Ceratophyllidae Orchopeas spp. 8 Siphonaptera Ceratophyllidae Orchopeas latens (Jordan) 1925 2 Siphonaptera Ceratophyllidae Orchopeas leucopus (Baker) 1904 2 Siphonaptera Ctenophthalmidae Anomiopsyllus falsicalifornicus C. Fox 1919 3 Siphonaptera Ctenophthalmidae Anomiopsyllus congruens Stewart 1940 96 incl. 38 Paratypes; syn. of A. falsicalifornicus Siphonaptera -
Insecta: Psocodea: 'Psocoptera'
Molecular systematics of the suborder Trogiomorpha (Insecta: Title Psocodea: 'Psocoptera') Author(s) Yoshizawa, Kazunori; Lienhard, Charles; Johnson, Kevin P. Citation Zoological Journal of the Linnean Society, 146(2): 287-299 Issue Date 2006-02 DOI Doc URL http://hdl.handle.net/2115/43134 The definitive version is available at www.blackwell- Right synergy.com Type article (author version) Additional Information File Information 2006zjls-1.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Blackwell Science, LtdOxford, UKZOJZoological Journal of the Linnean Society0024-4082The Lin- nean Society of London, 2006? 2006 146? •••• zoj_207.fm Original Article MOLECULAR SYSTEMATICS OF THE SUBORDER TROGIOMORPHA K. YOSHIZAWA ET AL. Zoological Journal of the Linnean Society, 2006, 146, ••–••. With 3 figures Molecular systematics of the suborder Trogiomorpha (Insecta: Psocodea: ‘Psocoptera’) KAZUNORI YOSHIZAWA1*, CHARLES LIENHARD2 and KEVIN P. JOHNSON3 1Systematic Entomology, Graduate School of Agriculture, Hokkaido University, Sapporo 060-8589, Japan 2Natural History Museum, c.p. 6434, CH-1211, Geneva 6, Switzerland 3Illinois Natural History Survey, 607 East Peabody Drive, Champaign, IL 61820, USA Received March 2005; accepted for publication July 2005 Phylogenetic relationships among extant families in the suborder Trogiomorpha (Insecta: Psocodea: ‘Psocoptera’) 1 were inferred from partial sequences of the nuclear 18S rRNA and Histone 3 and mitochondrial 16S rRNA genes. Analyses of these data produced trees that largely supported the traditional classification; however, monophyly of the infraorder Psocathropetae (= Psyllipsocidae + Prionoglarididae) was not recovered. Instead, the family Psyllipso- cidae was recovered as the sister taxon to the infraorder Atropetae (= Lepidopsocidae + Trogiidae + Psoquillidae), and the Prionoglarididae was recovered as sister to all other families in the suborder. -
Insecta: Phthiraptera) on Canada Geese (Branta Canadensis
Taxonomic, Ecological and Quantitative Examination of Chewing Lice (Insecta: Phthiraptera) on Canada Geese (Branta canadensis) and Mallards (Anas platyrhynchos) in Manitoba, Canada By Alexandra A. Grossi A thesis submitted to the Faculty of Graduate Studies of The University of Manitoba in partial fulfilment of the requirements of the degree of Masters of Science Department of Entomology University of Manitoba Winnipeg, Manitoba Copyright © 2013 by Alexandra A. Grossi 0 Abstract Over 19 years chewing lice data from Canada geese and mallards were collected. From Canada geese (n=300) 48,669 lice were collected, including Anaticola anseris, Anatoecus dentatus, Anatoecus penicillatus, Ciconiphilus pectiniventris, Ornithobius goniopleurus, and Trinoton anserinum. The prevalence of all lice on Canada geese was 92.3% and the mean intensity was 175.6 lice per bird. From mallards (n=269) 6,986 lice were collected which included: Anaticola crassicornis, A. dentatus, Holomenopon leucoxanthum, Holomenopon maxbeieri and Trinoton querquedulae. The prevalence of lice on mallards was 55.4% and the mean intensity was 42.0 lice per bird. Based on CO1, A. dentatus and Anatoecus icterodes were synonymised as A. dentatus. Anatoecus was found exclusively on the head, Anaticola was found predominantly on the wings, Ciconiphilus, Holomenopon and Ornithobius were observed in several body regions and Trinoton was found most often on the wings of mallards. i Acknowledgments I express my sincere thanks to my supervisor Dr. Terry Galloway for introducing me to the fascinating and complex world of chewing lice, and for his continued support and guidance throughout my thesis. I also like to thank my committee member Dr. -
Co-Extinct and Critically Co-Endangered Species of Parasitic Lice, and Conservation-Induced Extinction: Should Lice Be Reintroduced to Their Hosts?
Short Communication Co-extinct and critically co-endangered species of parasitic lice, and conservation-induced extinction: should lice be reintroduced to their hosts? L AJOS R ÓZSA and Z OLTÁN V AS Abstract The co-extinction of parasitic taxa and their host These problems highlight the need to develop reliable species is considered a common phenomenon in the current taxonomical knowledge about threatened and extinct global extinction crisis. However, information about the parasites. Although the co-extinction of host-specific conservation status of parasitic taxa is scarce. We present a dependent taxa (mutualists and parasites) and their hosts global list of co-extinct and critically co-endangered is known to be a feature of the ongoing wave of global parasitic lice (Phthiraptera), based on published data on extinctions (Stork & Lyal, 1993; Koh et al., 2004; Dunn et al., their host-specificity and their hosts’ conservation status 2009), the magnitude of this threat is difficult to assess. according to the IUCN Red List. We list six co-extinct Published lists of threatened animal parasites only cover and 40 (possibly 41) critically co-endangered species. ixodid ticks (Durden & Keirans, 1996; Mihalca et al., 2011), Additionally, we recognize 2–4 species that went extinct oestrid flies (Colwell et al., 2009), helminths of Brazilian as a result of conservation efforts to save their hosts. vertebrates (Muñiz-Pereira et al., 2009) and New Zealand Conservationists should consider preserving host-specific mites and lice (Buckley et al., 2012). Our aim here is to lice as part of their efforts to save species. provide a critical overview of the conservation status of parasitic lice. -
Volume 2, Chapter 12-5: Terrestrial Insects: Hemimetabola-Notoptera
Glime, J. M. 2017. Terrestrial Insects: Hemimetabola – Notoptera and Psocoptera. Chapter 12-5. In: Glime, J. M. Bryophyte Ecology. 12-5-1 Volume 2. Interactions. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. eBook last updated 19 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 12-5 TERRESTRIAL INSECTS: HEMIMETABOLA – NOTOPTERA AND PSOCOPTERA TABLE OF CONTENTS NOTOPTERA .................................................................................................................................................. 12-5-2 Grylloblattodea – Ice Crawlers ................................................................................................................. 12-5-3 Grylloblattidae – Ice Crawlers ........................................................................................................... 12-5-3 Galloisiana ................................................................................................................................. 12-5-3 Grylloblatta ................................................................................................................................ 12-5-3 Grylloblattella ............................................................................................................................ 12-5-4 PSOCOPTERA – Booklice, Barklice, Barkflies .............................................................................................. 12-5-4 Summary ......................................................................................................................................................... -
J. Judson Wynne, Ph.D. PROFESSIONAL PREPARATION
J. Judson Wynne, Ph.D. CURRICULUM VITAE The SETI Institute, Carl Sagan Center 189 Bernardo Ave., Mountain View, CA 94043 Phone: 928.863.8628 (cell), Email: [email protected], Web: http://www.jutwynne.com PROFESSIONAL PREPARATION Northern Arizona University (2014) Ph.D. Biological Sciences; emphasis ecology Title: On Sampling, Habitat and Relict Species of Cave-dwelling Arthropods of the American Southwest and Easter Island Northern Arizona University (2003) M.S. EnvironMental Science and Policy; eMphasis wildlife ecology and reMote sensing Title: Landscape-scale Modeling of Vegetation Land Cover and Songbird Habitat, Pinaleños Mountains, Arizona Vrije Universiteit Brussel, BelGium (1998) Certificate in Ecotechnie (Distinction: Magna cum laude) UNESCO-Cousteau European Postgraduate PrograMMe of Ecotechnie GeorGia Southern University (1993) B.S. Major: CoMMunications, Minor: Anthropology PUBLICATIONS Peer-Reviewed Publications (16) Harvey, M.S. and J.J. Wynne. In Press. Cave-dwelling Pseudoscorpions (Arachnida, Pseudoscorpiones) of Arizona, with descriptions of two short-range endeMic species froM North RiM Grand Canyon. Journal of Arachnology. Wynne, J.J., E.C. Bernard, F.G. Howarth, S. SoMMer, F.N. Soto-AdaMes, S. Taiti, E.L. Mockford, M. Horrocks, L. Pakarati, and V. Pakarati-Hotus. 2014. Disturbance relicts in a rapidly changing world: the Rapa Nui (Easter Island) factor. BioScience 64: 711–718. Wynne, J.J. and K.D. Voyles. 2014. Cave-dwelling arthropods and vertebrates of North RiM Grand Canyon, with notes on ecology and Management. Western North American Naturalist 74: 1–17. Wynne, J.J. 2014. Reign of the Red Queen: The future of bats hangs in the balance. The Explorers Journal 92: 40–45. -
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). -
Psocoptera of Muogamarra Nature Reserve
AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS Smithers, C. N., 1977. Psocoptera of Muogamarra Nature Reserve. Records of the Australian Museum 31(7): 251–306. [31 December 1977]. doi:10.3853/j.0067-1975.31.1977.215 ISSN 0067-1975 Published by the Australian Museum, Sydney naturenature cultureculture discover discover AustralianAustralian Museum Museum science science is is freely freely accessible accessible online online at at www.australianmuseum.net.au/publications/www.australianmuseum.net.au/publications/ 66 CollegeCollege Street,Street, SydneySydney NSWNSW 2010,2010, AustraliaAustralia THE PSOCOPTERA OF MUOGAMARRA NATURE RESERVE by C. N. SMITHERS The Australian Museum, Sydney SUMMARY In a preliminary study Psocoptera were periodically collected from eight habitats in Muogamarra Nature Reserve, near Sydney. Forty-three species were taken of which fifteen are described as new. Rainforest and Casuarina habitats yielded the greatest variety of species. Populations were highest in summer on Casuarina and showed little seasonal variation in rainforest; dry sclerophyll habitats, on the other hand, yielded greater populations in winter than summer. In each habitat one or two species were dominant. Acacia floribunda and Eucalyptus spp. were poorest in species and specimens. INTRODUCTION During the latter part of 1973 and through most of 1974 collections of Psocoptera were made at intervals from selected habitats in Muogamarra Nature Reserve. Psocoptera had not previously been recorded from the Reserve. The object of the work was to ascertain which species were present and to obtain some indication of any gross habitat preferences or seasonal fluctuations in numbers, if any, as a basis for planning future, more detailed, biological and ecological work. The basic information necessary for rational planning of such work has not been available for Australian species and very little appropriate work which might be applicable to Australian conditions has been done elsewhere. -
XII Dr. S. Pradhan Memorial Lecture Entomofauna, Ecosystem And
XII Dr. S. Pradhan Memorial Lecture September 28, 2020 Entomofauna, Ecosystem and Economics by Dr. Kailash Chandra, Director, Zoological Survey of India, Kolkata DIVISION OF ENTOMOLOGY, ICAR-INDIAN AGRICULTURAL RESEARCH INSTITUTE, NEW DELHI- 110012 ORGANIZING COMMITTEE PATRON Dr. A. K. Singh, Director, ICAR-IARI, New Delhi CONVENER Dr. Debjani Dey, Head (Actg.), Division of Entomology MEMBERS Dr. H. R. Sardana, Director, ICAR-NCIPM, New Delhi Dr. Subhash Chander, Professor & Principal Scientist Dr. Bishwajeet Paul, Principal Scientist Dr. Naresh M. Meshram, Senior Scientist Mrs. Rajna S, Scientist Dr. Bhagyasree S N, Scientist Dr. S R Sinha, CTO Shri Sushil Kumar, AAO (Member Secretary) XIII Dr. S. Pradhan Memorial Lecture September 28, 2020 Entomofauna, Ecosystem and Economics by Dr. Kailash Chandra, Director, Zoological Survey of India, Kolkata DIVISION OF ENTOMOLOGY, ICAR-INDIAN AGRICULTURAL RESEARCH INSTITUTE, NEW DELHI- 110012 Dr. S. Pradhan May 13, 1913 - February 6, 1973 4 Dr. S. Pradhan - A Profile Dr. S. Pradhan, a doyen among entomologists, during his 33 years of professional career made such an impact on entomological research and teaching that Entomology and Plant Protection Science in India came to the forefront of agricultural research. His success story would continue to enthuse Plant Protection Scientists of the country for generations to come. The Beginning Shyam Sunder Lal Pradhan had a humble beginning. He was born on May 13, 1913, at village Dihwa in Bahraich district of Uttar Pradesh. He came from a middle class family. His father, Shri Gur Prasad Pradhan, was a village level officer of the state Government having five sons and three daughters.