The Stained-Glass Moth, Samea Ecclesialis Guenée (Lepidoptera: Crambidae)1 James E
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A New Macrolepidopteran Moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican Amber
ZooKeys 965: 73–84 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.965.54461 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research A new macrolepidopteran moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican amber Weiting Zhang1,2, Chungkun Shih3,4, YuHong Shih5, Dong Ren3 1 Hebei GEO University, 136 Huaiandonglu, Shijiazhuang 050031, China 2 State Key Laboratory of Pal- aeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, CAS, Nanjing 210008, China 3 College of Life Sciences and Academy for Multidisciplinary Studies, Capital Normal University, 105 Xisan- huanbeilu, Haidian District, Beijing 100048, China 4 Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, USA 5 Laboratorio Dominicano De Ambar Y Gemas, Santo Domingo, Dominican Republic Corresponding author: Weiting Zhang ([email protected]) Academic editor: Gunnar Brehm | Received 19 May 2020 | Accepted 12 August 2020 | Published 3 September 2020 http://zoobank.org/05E273DB-B590-42D1-8234-864A787BE6A0 Citation: Zhang W, Shih C, Shih YH, Ren D (2020) A new macrolepidopteran moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican amber. ZooKeys 965: 73–84. https://doi.org/10.3897/zookeys.965.54461 Abstract A new genus and species of fossil moth, Miogeometrida chunjenshihi Zhang, Shih & Shih, gen. et sp. nov., assigned to Geometridae, is described from Miocene Dominican amber dating from 15–20 Mya. The new genus is characterized by the forewing without a fovea, R1 not anastomosing with Sc, no areole formed by veins R1 and Rs, R1 and Rs1 completely coincident, M2 arising midway between M1 and M3, anal veins 1A and 2A fused for their entire lengths; and the hind wing with Rs running close to Sc + R1 and M2 absent. -
NSW Weeds Conference Program
16th NSW Weeds Conference Proceedings 18th - 21st of July, 2011 Pacific Bay Conference Centre, Coffs Harbour Proudly hosted by Thank you to our Gold Sponsors Silver Sponsor Bronze Sponsors Introduction: The NSW Weeds Conference held in Coffs harbour 18-22 June 2011, is the 16th in a series organised by NSW Department of Primary Industries in partnership with various other organisations. The 2011 Conference was organised in partnership with Coffs Harbour City Council, NSW North Coast Weeds Advisory Committee, The Weed Society of NSW Inc. and NSW Weed Officers Association. Organising Committee: Rod Ensbey, NSW Department of Primary Industries Birgitte Verbeek, NSW Department of Primary Industries Tony Cook, NSW Department of Primary Industries Warwick Felton, Weeds Society of New South Wales Inc. Tim Scanlon, National Parks & Wildlife Service Reece Luxton, Clarence Valley Council David Merrikin, Northern Rivers Catchment Management Authority Ian Turnbull, Bellingen Shire Council Barry Powells, Coffs Harbour City Council Conference organiser: Michelle Aubert, Coffs Harbour City Council Citation: Proceedings of 16th NSW Weeds Conference, Coffs Harbour, July 2011 Disclaimer: The contents of these proceedings have undergone limited editorial or peer review. Papers have been critiqued (reviewers) for incorrect information, excessively controversial content and politically sensitive or libellous information prior to their publication. Paper Reviewers: Rod Ensbey Birgitte Verbeek Elissa van Oosterhout Phillip Blackmore Alan Maguire Peter Gray Tony Cook ISBN 978 1 74256 211 7 Monday 18th of July Registration from 4.30pm – Foyer Pacific Bay Conference Centre. Welcome Reception 5.30pm – 7.00pm Amongst the trade display, Pacific Bay Conference Centre. Day 1 – Tuesday 19th of July Opening Session - Auditorium Chair Bruce Christie, Principal Director Biosecurity NSW DPI 8.30 Welcome to Country 8.35 Conference Welcome – Mayor Keith Rhoades, Coffs Harbour City Council, President of the Local Government Association 8.45 Conference Opening - Minister for Primary Industries, Hon. -
Lepidoptera of North America 5
Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains, -
European Corn Borer, Ostrinia Nubilalis (Hübner) (Insecta: Lepidoptera: Crambidae)1 John L
EENY156 European Corn Borer, Ostrinia nubilalis (Hübner) (Insecta: Lepidoptera: Crambidae)1 John L. Capinera2 Distribution flights and oviposition typically occur in May, late June, and August. In locations with four generations, adults are active First found in North America near Boston, Massachusetts in April, June, July, and August-September. in 1917, European corn borer, Ostrinia nubilalis (Hübner), now has spread as far west as the Rocky Mountains in both Egg Canada and the United States, and south to the Gulf Coast Eggs are deposited in irregular clusters of about 15 to 20. states. European corn borer is thought to have originated in The eggs are oval, flattened, and creamy white in color, Europe, where it is widespread. It also occurs in northern usually with an iridescent appearance. The eggs darken Africa. The North American European corn borer popula- to a beige or orangish tan color with age. Eggs normally tion is thought to have resulted from multiple introductions are deposited on the underside of leaves, and overlap like from more than one area of Europe. Thus, there are at least shingles on a roof or fish scales. Eggs measure about 1.0 two, and possibly more, strains present. This species occurs mm in length and 0.75 m in width. The developmental infrequently in Florida. threshold for eggs is about 15°C. Eggs hatch in four to nine days. Life Cycle and Description The number of generations varies from one to four, with only one generation occurring in northern New England and Minnesota and in northern areas of Canada, whereas three to four generations occur in Virginia and other southern locations. -
Insect Survey of Four Longleaf Pine Preserves
A SURVEY OF THE MOTHS, BUTTERFLIES, AND GRASSHOPPERS OF FOUR NATURE CONSERVANCY PRESERVES IN SOUTHEASTERN NORTH CAROLINA Stephen P. Hall and Dale F. Schweitzer November 15, 1993 ABSTRACT Moths, butterflies, and grasshoppers were surveyed within four longleaf pine preserves owned by the North Carolina Nature Conservancy during the growing season of 1991 and 1992. Over 7,000 specimens (either collected or seen in the field) were identified, representing 512 different species and 28 families. Forty-one of these we consider to be distinctive of the two fire- maintained communities principally under investigation, the longleaf pine savannas and flatwoods. An additional 14 species we consider distinctive of the pocosins that occur in close association with the savannas and flatwoods. Twenty nine species appear to be rare enough to be included on the list of elements monitored by the North Carolina Natural Heritage Program (eight others in this category have been reported from one of these sites, the Green Swamp, but were not observed in this study). Two of the moths collected, Spartiniphaga carterae and Agrotis buchholzi, are currently candidates for federal listing as Threatened or Endangered species. Another species, Hemipachnobia s. subporphyrea, appears to be endemic to North Carolina and should also be considered for federal candidate status. With few exceptions, even the species that seem to be most closely associated with savannas and flatwoods show few direct defenses against fire, the primary force responsible for maintaining these communities. Instead, the majority of these insects probably survive within this region due to their ability to rapidly re-colonize recently burned areas from small, well-dispersed refugia. -
(Amsel, 1954) (Lepidoptera: Pyralidae, Phycitinae) – a New Species for the Croatian Pyraloid Moth Fauna, with an Updated Checklist
NAT. CROAT. VOL. 30 No 1 37–52 ZAGREB July 31, 2021 original scientific paper / izvorni znanstveni rad DOI 10.20302/NC.2021.30.4 PSOROSA MEDITERRANELLA (AMSEL, 1954) (LEPIDOPTERA: PYRALIDAE, PHYCITINAE) – A NEW SPECIES FOR THE CROATIAN PYRALOID MOTH FAUNA, WITH AN UPDATED CHECKLIST DANIJELA GUMHALTER Azuritweg 2, 70619 Stuttgart, Germany (e-mail: [email protected]) Gumhalter, D.: Psorosa mediterranella (Amsel, 1954) (Lepidoptera: Pyralidae, Phycitinae) – a new species for the Croatian pyraloid moth fauna, with an updated checklist. Nat. Croat., Vol. 30, No. 1, 37–52, 2021, Zagreb. From 2016 to 2020 numerous surveys were undertaken to improve the knowledge of the pyraloid moth fauna of Biokovo Nature Park. On August 27th, 2020 one specimen of Psorosa mediterranella (Amsel, 1954) from the family Pyralidae was collected on a small meadow (985 m a.s.l.) on Mt Biok- ovo. In this paper, the first data about the occurrence of this species in Croatia are presented. The previ- ous mention in the literature for Croatia was considered to be a misidentification of the past and has thus not been included in the checklist of Croatian pyraloid moth species. P. mediterranella was recorded for the first time in Croatia in recent investigations and, after other additions to the checklist have been counted, is the 396th species in the Croatian pyraloid moth fauna. An overview of the overall pyraloid moth fauna of Croatia is given in the updated species list. Keywords: Psorosa mediterranella, Pyraloidea, Pyralidae, fauna, Biokovo, Croatia Gumhalter, D.: Psorosa mediterranella (Amsel, 1954) (Lepidoptera: Pyralidae, Phycitinae) – nova vrsta u hrvatskoj fauni Pyraloidea, s nadopunjenim popisom vrsta. -
Nota Lepidopterologica
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Nota lepidopterologica Jahr/Year: 2005 Band/Volume: 28 Autor(en)/Author(s): Agassiz David J.L. Artikel/Article: Book Review Barry Goater, Matthias Nuss & Wolfgang Speidel. Pyraloidea I (Crambidae: Acentropinae, Evergestinae, Heliothelinae, Schoenobiinae, Scopariinae). - In: Peter Huemer & Ole Karsholt (eds.), Microlepidoptera of Europe, Volume 4 161-162 ©Societas Europaea Lepidopterologica; download unter http://www.biodiversitylibrary.org/ und www.zobodat.at Notalepid. 28 (3/4): 159-161 161 The species was described from 24 cT and 29 collected on Tagarsky island (river Yenisey, near Minusinsk). Afterwards, it was only mentioned as a member of Cossidae (Daniel 1955; Schoorl 1990; Yakovlev 2004), and only on the basis of the detailed original description. After a thorough analysis of Koshantschikov's description, Vladimir V. Dubatolov (Novosibirsk, Russia) assumed that the taxon could belong to Brachodidae. The same assumption was admitted by Axel Kallies (Australia). My study of the type material shows that the taxon does in fact belong to Brachodidae and that it is conspecific with Brachodes appendiculata (Esper, 1783), a species known from South and Central Europe, southern Urals, northern Kazakhstan, and southern Siberia (Zagulyaev 1978). Acknowledgements I am grateful to S. Yu. Sinev (St. Petersburg) for his help during my work with the type material of the Zoological Institute, Russian Academy of Sciences, to V. V. Dubatolov (Novosibirsk) and Axel Kallies (Australia) for their fruitful comments on the analysis of the Stygia gerassimovii description, to J. W. Schoorl jr. (Holland) for his help in my search for rare publications, to Thomas Witt (Germany) for his all-round support of this investigation, and to V. -
Evergestis Alborivulalis (Eversmann, 1843) in the Palaearctic (Lepidoptera: Crambidae, Evergestinae)
Natura Somogyiensis 23 211-220 Ka pos vár, 2013 Disjunct distribution of Evergestis alborivulalis (Eversmann, 1843) in the Palaearctic (Lepidoptera: Crambidae, Evergestinae) FAZEKAS IMRE Regiograf Institute, Majális tér 17/A, H-300 Komló, Hungary, e-mail: [email protected] FAZEKAS , I.: Disjunct distribution of Evergestis alborivulalis (Eversmann, 1843) in the Palaearctic. Abstract: Data on the geographical distribution of Evergestis alborivulalis (Eversmann, 1843) in Palaearctic are given, with maps. Biological data and habitats of the species are presented. Structure of genitalia and morphological characteristic of wings are illustrated in colour. With 13 figures. Keywords: Lepidoptera, Crambidae, Evergestis alborivulalis, bionomics, distribution, Palaearctic. Introduction The distribution patterns and life cycle of Evergestis alborivulalis have been of long- standing interest to researchers. The species was originally described from Russian material from the Ural region (EVERSMANN 1843). Systematically, E. alborivulalis belongs to the order Lepidoptera, family Crambidae, subfamily Evergestinae. There is very little information about the geographical range and bionomics of this species. Nobody has ever correlated and mapped distributional information already published in different works. Here, a map of its distribution in Eurasia is shown. Even though it is inevitably sketchy, it demonstrates the highly localised occurrence of E. alborivulalis. Until now, there has been no information about the larva and food plant, and little was known about the habitat preferences. In the last few years, intensive and systematic surveys in Hungary have been made by the author. Our database can be found in text. Detailed information can now be given about the habitat in Hungary. Natura 2000 habi- tat types of priority interest for the conservation of this moth have been selected. -
Butterflies and Moths of Dorchester County, Maryland, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Bionomics of Bagworms (Lepidoptera: Psychidae)
ANRV363-EN54-11 ARI 27 August 2008 20:44 V I E E W R S I E N C N A D V A Bionomics of Bagworms ∗ (Lepidoptera: Psychidae) Marc Rhainds,1 Donald R. Davis,2 and Peter W. Price3 1Department of Entomology, Purdue University, West Lafayette, Indiana, 47901; email: [email protected] 2Department of Entomology, Smithsonian Institution, Washington D.C., 20013-7012; email: [email protected] 3Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona, 86011-5640; email: [email protected] Annu. Rev. Entomol. 2009. 54:209–26 Key Words The Annual Review of Entomology is online at bottom-up effects, flightlessness, mating failure, parthenogeny, ento.annualreviews.org phylogenetic constraint hypothesis, protogyny This article’s doi: 10.1146/annurev.ento.54.110807.090448 Abstract Copyright c 2009 by Annual Reviews. The bagworm family (Lepidoptera: Psychidae) includes approximately All rights reserved 1000 species, all of which complete larval development within a self- 0066-4170/09/0107-0209$20.00 enclosing bag. The family is remarkable in that female aptery occurs in ∗The U.S. Government has the right to retain a over half of the known species and within 9 of the 10 currently recog- nonexclusive, royalty-free license in and to any nized subfamilies. In the more derived subfamilies, several life-history copyright covering this paper. traits are associated with eruptive population dynamics, e.g., neoteny of females, high fecundity, dispersal on silken threads, and high level of polyphagy. Other salient features shared by many species include a short embryonic period, developmental synchrony, sexual segrega- tion of pupation sites, short longevity of adults, male-biased sex ratio, sexual dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case. -
Big Creek Lepidoptera Checklist
Big Creek Lepidoptera Checklist Prepared by J.A. Powell, Essig Museum of Entomology, UC Berkeley. For a description of the Big Creek Lepidoptera Survey, see Powell, J.A. Big Creek Reserve Lepidoptera Survey: Recovery of Populations after the 1985 Rat Creek Fire. In Views of a Coastal Wilderness: 20 Years of Research at Big Creek Reserve. (copies available at the reserve). family genus species subspecies author Acrolepiidae Acrolepiopsis californica Gaedicke Adelidae Adela flammeusella Chambers Adelidae Adela punctiferella Walsingham Adelidae Adela septentrionella Walsingham Adelidae Adela trigrapha Zeller Alucitidae Alucita hexadactyla Linnaeus Arctiidae Apantesis ornata (Packard) Arctiidae Apantesis proxima (Guerin-Meneville) Arctiidae Arachnis picta Packard Arctiidae Cisthene deserta (Felder) Arctiidae Cisthene faustinula (Boisduval) Arctiidae Cisthene liberomacula (Dyar) Arctiidae Gnophaela latipennis (Boisduval) Arctiidae Hemihyalea edwardsii (Packard) Arctiidae Lophocampa maculata Harris Arctiidae Lycomorpha grotei (Packard) Arctiidae Spilosoma vagans (Boisduval) Arctiidae Spilosoma vestalis Packard Argyresthiidae Argyresthia cupressella Walsingham Argyresthiidae Argyresthia franciscella Busck Argyresthiidae Argyresthia sp. (gray) Blastobasidae ?genus Blastobasidae Blastobasis ?glandulella (Riley) Blastobasidae Holcocera (sp.1) Blastobasidae Holcocera (sp.2) Blastobasidae Holcocera (sp.3) Blastobasidae Holcocera (sp.4) Blastobasidae Holcocera (sp.5) Blastobasidae Holcocera (sp.6) Blastobasidae Holcocera gigantella (Chambers) Blastobasidae -
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.