Nota Lepidopterologica
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SYSTEMATICS of the MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of T
SYSTEMATICS OF THE MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of the Requirements for The Degree of Doctor of Philosophy in the Graduate School of The Ohio State University By Sibyl Rae Bucheli, M.S. ***** The Ohio State University 2005 Dissertation Committee: Approved by Dr. John W. Wenzel, Advisor Dr. Daniel Herms Dr. Hans Klompen _________________________________ Dr. Steven C. Passoa Advisor Graduate Program in Entomology ABSTRACT The phylogenetics, systematics, taxonomy, and biology of Gelechioidea (Insecta: Lepidoptera) are investigated. This superfamily is probably the second largest in all of Lepidoptera, and it remains one of the least well known. Taxonomy of Gelechioidea has been unstable historically, and definitions vary at the family and subfamily levels. In Chapters Two and Three, I review the taxonomy of Gelechioidea and characters that have been important, with attention to what characters or terms were used by different authors. I revise the coding of characters that are already in the literature, and provide new data as well. Chapter Four provides the first phylogenetic analysis of Gelechioidea to include molecular data. I combine novel DNA sequence data from Cytochrome oxidase I and II with morphological matrices for exemplar species. The results challenge current concepts of Gelechioidea, suggesting that traditional morphological characters that have united taxa may not be homologous structures and are in need of further investigation. Resolution of this problem will require more detailed analysis and more thorough characterization of certain lineages. To begin this task, I conduct in Chapter Five an in- depth study of morphological evolution, host-plant selection, and geographical distribution of a medium-sized genus Depressaria Haworth (Depressariinae), larvae of ii which generally feed on plants in the families Asteraceae and Apiaceae. -
St Julians Park Species List, 1984 – 2003
St Julians Park Species List, 1984 – 2003 Fungi Species Common Name Date recorded Scleroderma citrinum Common Earth Ball 19/09/99 Amillaria mellea Honey Fungus 19/09/99 Hypholoma sublateridium Brick Caps 19/09/99 Piptoporus belulinus Birch Polypore 19/09/99 Lycoperdon perlatum Common Puffball 19/09/99 Coriolus versicolor Many-Zoned Polypore 19/09/99 Boletus erythropus - 19/09/99 Lactarius quietus Oak/Oily Milk Cap 19/09/99 Russula cyanoxantha The Charcoal Burner 19/09/99 Amanita muscaria Fly Agaric 19/09/99 Laccaria laccata Deceiver 19/09/99 Lepidoptera Species Common Name Date recorded Melanargia galathea Marbled White 1992/3 Venessa cardui Painted Lady 1992/3 Thymelicus sylvestris Small Skipper 1992/3, 06/06/98 Ochlodes venata Large Skipper 1992/3, 06/06/98 Pararge aegeria Speckled Wood 1992/3, 06/06/98 Venessa atalanta Red Admiral 1992/3 Aglais urticae Small Tortoiseshell 1992/3 Polyommatus icarus Common Blue 1992/3, 06/06/98 Pyronia tithonus Gamekeeper 1992/3 Maniola jurtina Meadow Brown 1992/3, 06/06/98 Aphantopus hyperantus Ringlet 1992/3, 06/06/98 Inachis 10 Peacock 1992/3, 23/03/00 Polygonia C-album Comma 1992/3, 23/03/00 Anthocaris cardamines Orange Tip 1992/3 Noctua pronuba Large Yellow Underwing 06/06/98 Pieris brassicae Large White 06/06/98 Zygaena trifolii 5 Spot Burnet 06/06/98 Diboba caeruleocephala Figure of Eight 22/10/99 Xanthia aurago Barred Sallow 22/10/99 Chloroclysta truncate Common Marbled Carpet 22/10/99 Epirrata dilutata November Moth 22/10/99 Epirrata chrysti Pale November Moth 22/10/99, 07/11/99 Chloroclysta -
Island Biology Island Biology
IIssllaanndd bbiioollooggyy Allan Sørensen Allan Timmermann, Ana Maria Martín González Camilla Hansen Camille Kruch Dorte Jensen Eva Grøndahl, Franziska Petra Popko, Grete Fogtmann Jensen, Gudny Asgeirsdottir, Hubertus Heinicke, Jan Nikkelborg, Janne Thirstrup, Karin T. Clausen, Karina Mikkelsen, Katrine Meisner, Kent Olsen, Kristina Boros, Linn Kathrin Øverland, Lucía de la Guardia, Marie S. Hoelgaard, Melissa Wetter Mikkel Sørensen, Morten Ravn Knudsen, Pedro Finamore, Petr Klimes, Rasmus Højer Jensen, Tenna Boye Tine Biedenweg AARHUS UNIVERSITY 2005/ESSAYS IN EVOLUTIONARY ECOLOGY Teachers: Bodil K. Ehlers, Tanja Ingversen, Dave Parker, MIchael Warrer Larsen, Yoko L. Dupont & Jens M. Olesen 1 C o n t e n t s Atlantic Ocean Islands Faroe Islands Kent Olsen 4 Shetland Islands Janne Thirstrup 10 Svalbard Linn Kathrin Øverland 14 Greenland Eva Grøndahl 18 Azores Tenna Boye 22 St. Helena Pedro Finamore 25 Falkland Islands Kristina Boros 29 Cape Verde Islands Allan Sørensen 32 Tristan da Cunha Rasmus Højer Jensen 36 Mediterranean Islands Corsica Camille Kruch 39 Cyprus Tine Biedenweg 42 Indian Ocean Islands Socotra Mikkel Sørensen 47 Zanzibar Karina Mikkelsen 50 Maldives Allan Timmermann 54 Krakatau Camilla Hansen 57 Bali and Lombok Grete Fogtmann Jensen 61 Pacific Islands New Guinea Lucía de la Guardia 66 2 Solomon Islands Karin T. Clausen 70 New Caledonia Franziska Petra Popko 74 Samoa Morten Ravn Knudsen 77 Tasmania Jan Nikkelborg 81 Fiji Melissa Wetter 84 New Zealand Marie S. Hoelgaard 87 Pitcairn Katrine Meisner 91 Juan Fernandéz Islands Gudny Asgeirsdottir 95 Hawaiian Islands Petr Klimes 97 Galápagos Islands Dorthe Jensen 102 Caribbean Islands Cuba Hubertus Heinicke 107 Dominica Ana Maria Martin Gonzalez 110 Essay localities 3 The Faroe Islands Kent Olsen Introduction The Faroe Islands is a treeless archipelago situated in the heart of the warm North Atlantic Current on the Wyville Thompson Ridge between 61°20’ and 62°24’ N and between 6°15’ and 7°41’ W. -
Natural History of Lepidoptera Associated with Bird Nests in Mid-Wales
Entomologist’s Rec. J. Var. 130 (2018) 249 NATURAL HISTORY OF LEPIDOPTERA ASSOCIATED WITH BIRD NESTS IN MID-WALES D. H. B OYES Bridge Cottage, Middletown, Welshpool, Powys, SY21 8DG. (E-mail: [email protected]) Abstract Bird nests can support diverse communities of invertebrates, including moths (Lepidoptera). However, the understanding of the natural history of these species is incomplete. For this study, 224 nests, from 16 bird species, were collected and the adult moths that emerged were recorded. The majority of nests contained moths, with 4,657 individuals of ten species recorded. Observations are made on the natural history of each species and some novel findings are reported. The absence of certain species is discussed. To gain deeper insights into the life histories of these species, it would be useful to document the feeding habits of the larvae in isolation. Keywords : Commensal, detritivore, fleas, moths, Tineidae. Introduction Bird nests represent concentrated pockets of organic resources (including dead plant matter, feathers, faeces and other detritus) and can support a diverse invertebrate fauna. A global checklist compiled by Hicks (1959; 1962; 1971) lists eighteen insect orders associated with bird nests, and a study in England identified over 120 insect species, spanning eight orders (Woodroffe, 1953). Moths are particularly frequent occupants of bird nests, but large gaps in knowledge and some misapprehensions remain. For example, Tineola bisselliella (Hummel, 1823) was widely thought to infest human habitations via bird nests, which acted as natural population reservoirs. However, it has recently been discovered that this non-native species seldom occurs in rural bird nests and can be regarded as wholly synanthropic in Europe, where it was introduced from Africa around the turn of the 19th century (Plarre & Krüger- Carstensen, 2011; Plarre, 2014). -
Yorkhill Green Spaces Wildlife Species List
Yorkhill Green Spaces Wildlife Species List April 2021 update Yorkhill Green Spaces Species list Draft list of animals, plants, fungi, mosses and lichens recorded from Yorkhill, Glasgow. Main sites: Yorkhill Park, Overnewton Park and Kelvinhaugh Park (AKA Cherry Park). Other recorded sites: bank of River Kelvin at Bunhouse Rd/ Old Dumbarton Rd, Clyde Expressway path, casual records from streets and gardens in Yorkhill. Species total: 711 Vertebrates: Amhibians:1, Birds: 57, Fish: 7, Mammals (wild): 15 Invertebrates: Amphipods: 1, Ants: 3, Bees: 26, Beetles: 21, Butterflies: 11, Caddisflies: 2, Centipedes: 3, Earthworms: 2, Earwig: 1, Flatworms: 1, Flies: 61, Grasshoppers: 1, Harvestmen: 2, Lacewings: 2, Mayflies: 2, Mites: 4, Millipedes: 3, Moths: 149, True bugs: 13, Slugs & snails: 21, Spiders: 14, Springtails: 2, Wasps: 13, Woodlice: 5 Plants: Flowering plants: 174, Ferns: 5, Grasses: 13, Horsetail: 1, Liverworts: 7, Mosses:17, Trees: 19 Fungi and lichens: Fungi: 24, Lichens: 10 Conservation Status: NameSBL - Scottish Biodiversity List Priority Species Birds of Conservation Concern - Red List, Amber List Last Common name Species Taxon Record Common toad Bufo bufo amphiban 2012 Australian landhopper Arcitalitrus dorrieni amphipod 2021 Black garden ant Lasius niger ant 2020 Red ant Myrmica rubra ant 2021 Red ant Myrmica ruginodis ant 2014 Buff-tailed bumblebee Bombus terrestris bee 2021 Garden bumblebee Bombus hortorum bee 2020 Tree bumblebee Bombus hypnorum bee 2021 Heath bumblebee Bombus jonellus bee 2020 Red-tailed bumblebee Bombus -
Laboratory Rearing of Agonopterix Alstroemeriana, the Defoliating
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Diposit Digital de Documents de la UAB PHYSIOLOGICAL ECOLOGY Laboratory Rearing of Agonopterix alstroemeriana, the Defoliating Poison Hemlock (Conium maculatum L.) Moth, and Effects of Piperidine Alkaloids on Preference and Performance 1 EVA CASTELLS AND MAY R. BERENBAUM Department of Entomology, University of Illinois at Urbana-Champaign, 320 Morrill Hall, 505 S Goodwin Ave., Urbana, IL 61801 Environ. Entomol. 35(3): 607Ð615 (2006) ABSTRACT Conium maculatum L. (Apiaceae), or poison hemlock, is an invasive plant native to Europe that has become extensively naturalized throughout North America. This species contains piperidine alkaloids, including coniine and ␥-coniceine, that are highly toxic to vertebrates. C. maculatum was relatively free from herbivores in North America until the accidental introduction 30 yr ago of its monophagous European associate Agonopterix alstroemeriana (Clerck) (Lepidoptera: Oecophoridae). At present, A. alstroemeriana is widespread across the United States, and in some areas, such as the Northwest, can inßict substantial damage on its host plant, leading to desiccation and death. A. alstroemeriana has been used in recent years for the biological control of C. maculatum, although its use has been limited by the availability of larvae, which are Þeld-collected from early to mid-spring, and by the lack of available information about its life history and feeding habits. Here we describe a laboratory-rearing protocol incorporating a simulated winter to induce diapause and a semideÞned artiÞcial diet that allows the production of multiple generations per year and enabled us to determine the number and duration of A. -
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. -
Harper's Island Wetlands Butterflies & Moths (2020)
Introduction Harper’s Island Wetlands (HIW) nature reserve, situated close to the village of Glounthaune on the north shore of Cork Harbour is well known for its birds, many of which come from all over northern Europe and beyond, but there is a lot more to the wildlife at the HWI nature reserve than birds. One of our goals it to find out as much as we can about all aspects of life, both plant and animal, that live or visit HIW. This is a report on the butterflies and moths of HIW. Butterflies After birds, butterflies are probably the one of the best known flying creatures. While there has been no structured study of them on at HIW, 17 of Ireland’s 33 resident and regular migrant species of Irish butterflies have been recorded. Just this summer we added the Comma butterfly to the island list. A species spreading across Ireland in recent years possibly in response to climate change. Hopefully we can set up regular monitoring of the butterflies at HIW in the next couple of years. Butterfly Species Recorded at Harper’s Island Wetlands up to September 2020. Colias croceus Clouded Yellow Pieris brassicae Large White Pieris rapae Small White Pieris napi Green-veined White Anthocharis cardamines Orange-tip Lycaena phlaeas Small Copper Polyommatus icarus Common Blue Celastrina argiolus Holly Blue Vanessa atalanta Red Admiral Vanessa cardui Painted Lady Aglais io Peacock Aglais urticae Small Tortoiseshell Polygonia c-album Comma Speyeria aglaja Dark-green Fritillary Pararge aegeria Speckled Wood Maniola jurtina Meadow Brown Aphantopus hyperantus Ringlet Moths One group of insects that are rarely seen by visitors to HIW is the moths. -
Depressariinae of Madeira and the Azores Islands (Lepidoptera: Depressariidae)
69 (2): 331 – 353 2019 © 2019 TheSenckenberg Authors Gesellschaft für Naturforschung Depressariinae of Madeira and the Azores Islands (Lepidoptera: Depressariidae) With 35 figures Peter Buchner 1 and Ole Karsholt 2 1 Scheibenstraße 335, A-2625 Schwarzau am Steinfeld, Austria. – [email protected] 2 Zoological Museum, Natural History Museum of Denmark, Universitetsparken 15, DK-2100 Copenhagen Ø, Denmark. – [email protected] Published on 2019–12–23 DOI: 10.21248/contrib.entomol.69.2.331-353 Abstract We review and illustrate the species of Depressariinae known from Madeira and the Azores Islands. The following six species are treated: Agonopterix scopariella (Heinemann, 1870), A. conciliatella (Rebel, 1892), A. vendettella (Chrétien, 1908) (new to Madeira), A. perezi Walsingham, 1908, Depressaria marcella Rebel, 1901 (new to Madeira and the Azores), and D. halophilella Chrétien, 1908. The latter replaces Depressaria ultimella Stainton, 1849 in the list of Lepidoptera found in Madeira. Depressaria iliensis Rebel, 1936 is a synonym of Agonopterix vendettella (Chrétien, 1908) (syn. nov.). Depressaria halophilella is new to the Canary Islands. We provide brief notes on each of the species and give short diagnoses for correctly identifying them, and we discuss previous misidentifications of Madeiran Depressariinae. Key words Lepidoptera, Depressariinae, Madeira, Azores Islands Zusammenfassung Wir überprüfen und illustrieren die von Madeira und den Azoren bekannten Depressariinae. Folgende sechs Arten werden behandelt: Agonopterix scopariella (Heinemann, 1870), A. conciliatella (Rebel, 1892), A. vendettella (Chrétien, 1908) (neu für Madeira), A. perezi Walsingham, 1908, Depressaria marcella Rebel, 1901 (neu für Madeira und die Azoren), und D. halophilella Chrétien, 1908. Letztere ersetzt Depressaria ultimella Stainton, 1849 in der Liste der von Madeira nachgewiesenen Lepidoptera. -
Why Mammals Are Called Mammals: Gender Politics in Eighteenth-Century Natural History Author(S): Londa Schiebinger Source: the American Historical Review, Vol
Why Mammals are Called Mammals: Gender Politics in Eighteenth-Century Natural History Author(s): Londa Schiebinger Source: The American Historical Review, Vol. 98, No. 2 (Apr., 1993), pp. 382-411 Published by: American Historical Association Stable URL: http://www.jstor.org/stable/2166840 Accessed: 22/01/2010 10:27 Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/page/info/about/policies/terms.jsp. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/action/showPublisher?publisherCode=aha. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. American Historical Association is collaborating with JSTOR to digitize, preserve and extend access to The American Historical Review. http://www.jstor.org Why Mammals Are Called Mammals: Gender Politics in Eighteenth-Century Natural History LONDA SCHIEBINGER IN 1758, IN THE TENTH EDITION OF HIS Systema naturae, Carolus Linnaeus introduced the term Mammaliainto zoological taxonomy. -
Additions, Deletions and Corrections to An
Bulletin of the Irish Biogeographical Society No. 36 (2012) ADDITIONS, DELETIONS AND CORRECTIONS TO AN ANNOTATED CHECKLIST OF THE IRISH BUTTERFLIES AND MOTHS (LEPIDOPTERA) WITH A CONCISE CHECKLIST OF IRISH SPECIES AND ELACHISTA BIATOMELLA (STAINTON, 1848) NEW TO IRELAND K. G. M. Bond1 and J. P. O’Connor2 1Department of Zoology and Animal Ecology, School of BEES, University College Cork, Distillery Fields, North Mall, Cork, Ireland. e-mail: <[email protected]> 2Emeritus Entomologist, National Museum of Ireland, Kildare Street, Dublin 2, Ireland. Abstract Additions, deletions and corrections are made to the Irish checklist of butterflies and moths (Lepidoptera). Elachista biatomella (Stainton, 1848) is added to the Irish list. The total number of confirmed Irish species of Lepidoptera now stands at 1480. Key words: Lepidoptera, additions, deletions, corrections, Irish list, Elachista biatomella Introduction Bond, Nash and O’Connor (2006) provided a checklist of the Irish Lepidoptera. Since its publication, many new discoveries have been made and are reported here. In addition, several deletions have been made. A concise and updated checklist is provided. The following abbreviations are used in the text: BM(NH) – The Natural History Museum, London; NMINH – National Museum of Ireland, Natural History, Dublin. The total number of confirmed Irish species now stands at 1480, an addition of 68 since Bond et al. (2006). Taxonomic arrangement As a result of recent systematic research, it has been necessary to replace the arrangement familiar to British and Irish Lepidopterists by the Fauna Europaea [FE] system used by Karsholt 60 Bulletin of the Irish Biogeographical Society No. 36 (2012) and Razowski, which is widely used in continental Europe. -
Records of Two New Palearctic Moth Species Associated with Queen Anne’S Lace in Nova Scotia
J. Acad. Entomol. Soc. 13: 54-57 (2017) NOTE Records of two new Palearctic moth species associated with Queen Anne’s lace in Nova Scotia Jeffrey Ogden Daucus carota Linnaeus, commonly known as Queen Anne’s lace or wild carrot, is native to Europe and southwestern Asia. It is believed to have been introduced to North America in soil ballast by the first European settlers (Lindroth 1957). It has historically been used as a food source and is the ancestral plant of our common cultivated garden carrot. Since its introduction, Daucus carota has spread widely and is common to much of North America. In Nova Scotia, this biennial is a very common plant of fields, roadsides and other weedy areas throughout the mainland and parts of Cape Breton (Zinck 1998). Previous insect surveys have recorded hundreds of species of insects attracted to the large white flower heads of the plant (Judd 1970; Largo & Mann 1987). Although considered a common weed species, Daucus carota is an important host to numerous beneficial insect species, including many pollinators and predatory species (Judd 1970). In this report, the first detections ofSitochroa palealis (Denis & Schiffermüller) (Lepidoptera: Crambidae), the carrot seed moth, and Depressaria depressana (Fabricius) (Lepidoptera: Depressariidae), the purple carrot seed moth, are described from Nova Scotia. Larvae of each species were collected within the flower heads of Daucus carota during the summers of 2015 to 2017. Adults were collected as part of an ongoing light trapping survey and through lab rearing. Verified photograph records were also considered. Voucher specimens have been deposited in the Nova Scotia Department of Natural Resources Reference Collection, the Nova Scotia Museum, and the author’s personal collection.