DOCSLIB.ORG

Butterflies and Moths of New Brunswick, Canada

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Butterflies and Moths of New Brunswick, Canada 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 Urbanus doryssus White-tailed Longtail Astraptes fulgerator Two-barred Flasher Astraptes egregius Small-spotted Flasher Astraptes alardus Frosted Flasher Astraptes habana Frosty Flasher Astraptes alector Gilbert's Flasher Astraptes anaphus Yellow-tipped Flasher Autochton cellus Golden Banded-Skipper Autochton pseudocellus Sonoran Banded-Skipper Autochton cincta Chisos Banded-Skipper Autochton vectilucis Central American Banded-Skipper Autochton neis Broad Banded-Skipper Autochton longipennis Spike Banded-Skipper Achalarus lyciades Hoary Edge Achalarus casica Desert Cloudywing Achalarus tehuacana Tehuacan or Dark Cloudywing Achalarus albociliatus Skinner's Cloudywing Achalarus toxeus Coyote Cloudywing Thessia jalapus Jalapus Cloudywing Thorybes drusius Drusius Cloudywing Thorybes pylades Northern Cloudywing Thorybes bathyllus Southern Cloudywing Thorybes confusis Confused Cloudywing Thorybes diversus Western Cloudywing Thorybes mexicana Mexican Cloudywing Cabares potrillo Potrillo Skipper Celaenorrhinus fritzgaertneri Fritzgaertner's Flat Celaenorrhinus stallingsi Stallings' Flat Celaenorrhinus stola Slota Flat Spathilepia clonius Falcate Skipper Cogia hippalus Acacia Skipper Cogia outis Outis Skipper Cogia caicus Gold-costa Skipper Cogia calchas Mimosa Skipper Bungalotis quadratum Pallid Scarlet-eye Arteurotia tractipennis Starred Skipper Polyctor cleta Cleta Tufted-Skipper Polyctor enops Enops Tufted-Skipper Nisoniades rubescens Purplish-black Skipper Pellicia arina Glazed Pellicia Pellicia dimidiata Morning Glory Pellicia Noctuana stator Red-studded Skipper Noctuana lactifera Cryptic Skipper Windia windi Wind's Skipper Bolla brennus Obscure Bolla Bolla eusebius Spatulate Sootywing Bolla clytius Mottled Bolla Staphylus ceos Golden-headed Scallopwing Staphylus vulgata Golden-snouted Sootywing Staphylus hayhurstii Hayhurst's Scallopwing Staphylus mazans Mazans Scallopwing Staphylus ascalaphus Central American Sootywing or Mauve Scallopwing Staphylus azteca Aztec Scallopwing Gorgythion begga Variegated Skipper Sostrata nordica Blue-studded Skipper Paches polla Polla Blue-Skipper Carrhenes canescens Hoary Skipper Carrhenes fuscescens Tanned Hoary-Skipper Xenophanes tryxus Glassy-winged Skipper Onenses hyalophora Crystal-winged Skipper Antigonus emorsa White Spurwing Antigonus erosus Antigonus nearchus Large Spurwing Mylon pelopidas Pale Mylon / Dingy Mylon Mylon lassia Bold Mylon Systasea pulverulenta Texas Powdered Skipper Systasea zampa Arizona Powdered Skipper Achlyodes busirus heros Giant Sicklewing Achlyodes pallida Pale Sicklewing Eantis tamenund Northern Sicklewing Eantis papinianus Cuban Sicklewing Zera hyacinthinus Bruised Skipper Quadrus lugubris Tanned Blue-Skipper Atarnes sallei Orange-spotted Skipper Grais stigmaticus Hermit Skipper Timochares ruptifasciata Brown-banded Skipper Timochares trifasciata Many-banded Skipper Anastrus sempiternus Common Anastrus Anastrus neaeris neaeris Brilliant Anastrus Ebrietas anacreon Common Bent-Skipper Helias cama Squared Bent-Skipper Theagenes aegides White-centered Bent-Skipper Chiomara georgina White-patched Skipper Chiomara mithrax Slaty Skipper Gesta invisus False Duskywing Ephyriades zephodes Zephodes Duskywing Ephyriades arcas Caribbean Duskywing Ephyriades brunnea Florida Duskywing Erynnis icelus Dreamy Duskywing Erynnis brizo Sleepy Duskywing Erynnis juvenalis Juvenal's Duskywing Erynnis telemachus Rocky Mountain Duskywing Erynnis propertius Propertius Duskywing Erynnis meridianus Meridian Duskywing Erynnis scudderi Scudder's Duskywing Erynnis horatius Horace's Duskywing Erynnis tristis Mournful Duskywing Erynnis martialis Mottled Duskywing Erynnis pacuvius Pacuvius Duskywing Erynnis zarucco Zarucco Duskywing Erynnis funeralis Funereal Duskywing Erynnis baptisiae Wild Indigo Duskywing Erynnis lucilius Columbine Duskywing Erynnis afranius Afranius Duskywing Erynnis persius Persius Duskywing Aethilla lavochrea Yellow-rimmed Skipper Aethilla echina Echina Skipper Anisochoria bacchus Northern Snout-Skipper Pyrgus centaureae Grizzled Skipper Pyrgus ruralis Two-banded Checkered-Skipper Pyrgus xanthus Mountain Checkered-Skipper Pyrgus scriptura Small Checkered-Skipper Pyrgus communis Common Checkered-Skipper Pyrgus albescens White Checkered-Skipper Pyrgus adepta Central American Checkered-Skipper Pyrgus philetas Desert Checkered-Skipper Pyrgus oileus Tropical Checkered-Skipper Pyrgus crisia Antillean Checkered-Skipper Heliopyrgus domicella Erichson's White-Skipper Heliopyrgus sublinea Heliopetes ericetorum Northern White-Skipper Heliopetes macaira Turk's-cap White-Skipper Heliopetes laviana Laviana White-Skipper Heliopetes arsalte Veined White-Skipper Heliopetes alana Alana White-Skipper Celotes nessus Common Streaky-Skipper Celotes limpia Scarce Streaky-Skipper Pholisora catullus Common Sootywing Pholisora mejicanus Mexican Sootywing Hesperopsis libya Mohave Sootywing Hesperopsis alpheus Saltbush Sootywing Hesperopsis gracielae MacNeill's Sootywing Creonpyge creon Creon Skipper Carterocephalus palaemon Arctic Skipper Piruna pirus Russet Skipperling Piruna haferniki Chisos Skipperling Piruna polingii Four-spotted Skipperling Piruna aea Many-spotted Skipperling Piruna microstictus Small-spotted Skipperling Piruna penaea Hour-glass Skipperling Synapte malitiosa Malicious Skipper Synapte pecta Northern Faceted-Skipper Synapte syraces Bold Faceted Skipper Synapte shiva Faded Faceted Skipper Synapte salenus Salenus Skipper Anthoptus epictetus Trailside Skipper Corticea corticea Redundant Skipper Zariaspes mys Mys Skipper Vinius tryhana Gold-washed Skipper Apaustus gracilis Delicate Skipper Callimormus saturnus Saturnus Skipper Mnasicles geta Violet-frosted Skipper Vidius perigenes Pale-rayed Skipper Monca crispinus Violet-patched Skipper Nastra lherminier Swarthy Skipper Nastra neamathla Neamathla Skipper Nastra julia Julia's Skipper Cymaenes tripunctus Three-spotted Skipper Cymaenes alumna Alumna Skipper Cymaenes trebius Fawn-spotted Skipper Vehilius inca Inca Skipper Vehilius stictomenes Pasture Skipper Lerema accius Clouded Skipper Lerema ancillaris Liris Skipper Niconiades nikko Nikko Skipper Vettius fantasos Fantastic Skipper Joanna joanna Joanna's Skipper Perichares philetes Green-backed Ruby-eye Rhinthon osca Osca Skipper Rhinthon bushi Bush's Skipper Decinea percosius Double-dotted Skipper Decinea decinea Huastecan Skipper Orthos lycortas Lycortas Skipper Conga chydaea Hidden-ray Skipper Ancyloxypha numitor Least Skipper Ancyloxypha arene Tropical Least Skipper Oarisma garita Garita Skipperling Oarisma poweshiek Poweshiek Skipperling Oarisma edwardsii Edwards' Skipperling Copaeodes aurantiaca Orange Skipperling Copaeodes minima Southern Skipperling Adopaeoides prittwitzi Sunrise Skipper Thymelicus lineola European Skipper Hylephila phyleus Fiery Skipper Pseudocopaeodes eunus Alkali Skipper Stinga morrisoni Morrison's Skipper Hesperia uncas Uncas Skipper Hesperia juba Juba Skipper Hesperia comma Common Branded Skipper Hesperia assiniboia Plains Skipper Hesperia colorado Western Branded Skipper Hesperia woodgatei Apache Skipper Hesperia ottoe Ottoe Skipper Hesperia leonardus Leonard's Skipper Hesperia pahaska Pahaska Skipper Hesperia columbia Columbian Skipper Hesperia metea Cobweb Skipper Hesperia viridis Green Skipper Hesperia attalus Dotted Skipper Hesperia meskei Meske's Skipper Hesperia dacotae Dakota Skipper Hesperia lindseyi Lindsey's Skipper Hesperia sassacus Indian Skipper Hesperia miriamae Sierra Skipper Hesperia nevada Nevada Skipper Atalopedes campestris Sachem Atalopedes mesogramma Mesogramma Skipper Polites rhesus Rhesus Skipper Polites carus Carus Skipper Polites peckius Peck's Skipper Polites sabuleti Sandhill Skipper Polites draco Draco Skipper Polites mardon Mardon Skipper Polites themistocles Tawny-edged Skipper Polites baracoa Baracoa Skipper Polites origenes Crossline Skipper Polites mystic Long Dash Polites sonora Sonora Skipper Polites vibex Whirlabout Wallengrenia egeremet Northern Broken-Dash Wallengrenia otho Southern
Load more

Recommended publications
  • 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,
    [Show full text]
  • Eastern Persius Duskywing Erynnis Persius Persius
    COSEWIC Assessment and Status Report on the Eastern Persius Duskywing Erynnis persius persius in Canada ENDANGERED 2006 COSEWIC COSEPAC COMMITTEE ON THE STATUS OF COMITÉ SUR LA SITUATION ENDANGERED WILDLIFE DES ESPÈCES EN PÉRIL IN CANADA AU CANADA COSEWIC status reports are working documents used in assigning the status of wildlife species suspected of being at risk. This report may be cited as follows: COSEWIC 2006. COSEWIC assessment and status report on the Eastern Persius Duskywing Erynnis persius persius in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. vi + 41 pp. (www.sararegistry.gc.ca/status/status_e.cfm). Production note: COSEWIC would like to acknowledge M.L. Holder for writing the status report on the Eastern Persius Duskywing Erynnis persius persius in Canada. COSEWIC also gratefully acknowledges the financial support of Environment Canada. The COSEWIC report review was overseen and edited by Theresa B. Fowler, Co-chair, COSEWIC Arthropods Species Specialist Subcommittee. For additional copies contact: COSEWIC Secretariat c/o Canadian Wildlife Service Environment Canada Ottawa, ON K1A 0H3 Tel.: (819) 997-4991 / (819) 953-3215 Fax: (819) 994-3684 E-mail: COSEWIC/[email protected] http://www.cosewic.gc.ca Également disponible en français sous le titre Évaluation et Rapport de situation du COSEPAC sur l’Hespérie Persius de l’Est (Erynnis persius persius) au Canada. Cover illustration: Eastern Persius Duskywing — Original drawing by Andrea Kingsley ©Her Majesty the Queen in Right of Canada 2006 Catalogue No. CW69-14/475-2006E-PDF ISBN 0-662-43258-4 Recycled paper COSEWIC Assessment Summary Assessment Summary – April 2006 Common name Eastern Persius Duskywing Scientific name Erynnis persius persius Status Endangered Reason for designation This lupine-feeding butterfly has been confirmed from only two sites in Canada.
    [Show full text]
  • Conservation and Management of Eastern Big-Eared Bats a Symposium
    Conservation and Management of Eastern Big-eared Bats A Symposium y Edited b Susan C. Loeb, Michael J. Lacki, and Darren A. Miller U.S. Department of Agriculture Forest Service Southern Research Station General Technical Report SRS-145 DISCLAIMER The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. Papers published in these proceedings were submitted by authors in electronic media. Some editing was done to ensure a consistent format. Authors are responsible for content and accuracy of their individual papers and the quality of illustrative materials. Cover photos: Large photo: Craig W. Stihler; small left photo: Joseph S. Johnson; small middle photo: Craig W. Stihler; small right photo: Matthew J. Clement. December 2011 Southern Research Station 200 W.T. Weaver Blvd. Asheville, NC 28804 Conservation and Management of Eastern Big-eared Bats: A Symposium Athens, Georgia March 9–10, 2010 Edited by: Susan C. Loeb U.S Department of Agriculture Forest Service Southern Research Station Michael J. Lacki University of Kentucky Darren A. Miller Weyerhaeuser NR Company Sponsored by: Forest Service Bat Conservation International National Council for Air and Stream Improvement (NCASI) Warnell School of Forestry and Natural Resources Offield Family Foundation ContEntS Preface . v Conservation and Management of Eastern Big-Eared Bats: An Introduction . 1 Susan C. Loeb, Michael J. Lacki, and Darren A. Miller Distribution and Status of Eastern Big-eared Bats (Corynorhinus Spp .) . 13 Mylea L. Bayless, Mary Kay Clark, Richard C. Stark, Barbara S.
    [Show full text]
  • E-Acta Natzralia Pannonica
    e ● Acta Naturalia Pannonica e–Acta Nat. Pannon. 5: 39–46. (2013) 39 Hungarian Eupitheciini studies (No. 2) Records from Nattán’s collection (Lepidoptera: Geometridae) Imre Fazekas Abstract: Data on 37 species collected in Hungary are given. Additional data on faunistics, taxonomy and zoogeography of cer- tain species are provided by the author, with comments. Figures of the genitalia of some species are included. With 18 figures. Key words: Lepidoptera, Geometridae, Euptheciini, distribution, biology, Hungary. Author’s address: Imre Fazekas, Regiograf Institute, Majális tér 17/A, H-7300 Komló, Hungary. Introduction A detailed account of the Eupitheciini species in 20% KOH solution. Genitalia were cleaned and Hungary has been given in five previous works dehydrated in ethanol and mounted in Euparal (Fazekas 1977ab, 1979ab, 1980, 2012). To date 64 between microscope slides and cover slips. Illus- Hungarian Geometridae, tribus Eupitheciini are trations of adults were produced by a multi-layer known. technique using a Sony DSC HX100V with a 4x Present paper contains faunistical data of the Macro Conversion Lens. The photographs were Eupitheciini specimens in the Nattán collection (in processed by the software Photoshop CS3 version. coll. Janus Pannonius Museum, H-Pécs) that col- The genitalia illustrations were produced in a sim- lected outside of the South Transdanubia. ilar manner with multi-layer technique, using an- Miklós Nattán (1910–1970) was an amateur lep- other digital camera (BMS tCam 3,0 MP) and a idopterist who, over nearly six decades, made one XSP-151-T-LED Microscope with a plan lens 4/0.1 of the most significant private collections of Lepi- and 10/0.25.
    [Show full text]
  • The Associations Between Pteridophytes and Arthropods
    FERN GAZ. 12(1) 1979 29 THE ASSOCIATIONS BETWEEN PTERIDOPHYTES AND ARTHROPODS URI GERSON The Hebrew University of Jerusalem, Faculty of Agriculture, Rehovot, Israel. ABSTRACT Insects belonging to 12 orders, as well as mites, millipedes, woodlice and tardigrades have been collected from Pterldophyta. Primitive and modern, as well as general and specialist arthropods feed on pteridophytes. Insects and mites may cause slight to severe damage, all plant parts being susceptible. Several arthropods are pests of commercial Pteridophyta, their control being difficult due to the plants' sensitivity to pesticides. Efforts are currently underway to employ insects for the biological control of bracken and water ferns. Although Pteridophyta are believed to be relatively resistant to arthropods, the evidence is inconclusive; pteridophyte phytoecdysones do not appear to inhibit insect feeders. Other secondary compounds of preridophytes, like prunasine, may have a more important role in protecting bracken from herbivores. Several chemicals capable of adversely affecting insects have been extracted from Pteridophyta. The litter of pteridophytes provides a humid habitat for various parasitic arthropods, like the sheep tick. Ants often abound on pteridophytes (especially in the tropics) and may help in protecting these plants while nesting therein. These and other associations are discussed . lt is tenatively suggested that there might be a difference in the spectrum of arthropods attacking ancient as compared to modern Pteridophyta. The Osmundales, which, in contrast to other ancient pteridophytes, contain large amounts of ·phytoecdysones, are more similar to modern Pteridophyta in regard to their arthropod associates. The need for further comparative studies is advocated, with special emphasis on the tropics.
    [Show full text]
  • Chapter17 Appendixiii Species List.Pub
    Appendix 3: Species List English Latin French PLANTS Acadian quillwort Isoetes acadiensis Isoète acadien Alder Alnus sp. Aulne Alpine bilberry (bog blueberry) Vaccinium uliginosum Airelle des marécages Alternate-leaved dogwood Cornus alternifolia Cornouiller à feuilles alternes American mountain-ash Sorbus americana Sorbier d’Amérique (cormier) American red currant Ribes triste Gadellier amer Arctic sweet coltsfoot Petasites frigidus Pétasite palmé (pétasite hybride) Arrow-grass Triglochin sp. Troscart Ash Fraxinus sp. Frêne Aspen Populus sp. Tremble Atlantic manna grass Glyceria obtusa Glycérie Awlwort Subularia aquatica Subulaire aquatique Back’s sedge Carex backii Carex de Back Bake-apple (cloudberry) Rubus chamaemorus Ronce petit-mûrier (mûres blanches) Balsam fir Abies balsamea Sapin baumier Balsam poplar Populus balsamifera Peuplier baumier (liard) Basswood (American linden) Tilia americana Tilleul d’Amérique (bois blanc) Bathurst saltmarsh aster Aster subulatus var. obtusifolius Aster subulé Beaked hazelnut Corylus cornuta Noisetier à long bec Beech (American beech) Fagus grandifolia Hêtre à grandes feuilles (hêtre américain) Bigelow’s sedge Carex bigelowii Carex de Bigelow Birch Betula sp. Bouleau Black ash Fraxinus nigra Frêne noir Black cherry Prunus serotina Cerisier Tardif Black crowberry Empetrum nigrum Camarine noire (Graines à corbigeaux) Black grass Juncus gerardii Jonc de Gérard Black spruce Picea mariana Épinette noire Black willow Salix nigra Saule noir Bloodroot Sanguinaria canadensis Sanguinaire du Canada (sang-dragon)
    [Show full text]
  • Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometro
    Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, & Noctuoidea) Biodiversity Inventory of the University of Florida Natural Area Teaching Lab Hugo L. Kons Jr. Last Update: June 2001 Abstract A systematic check list of 489 species of Lepidoptera collected in the University of Florida Natural Area Teaching Lab is presented, including 464 species in the superfamilies Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, and Noctuoidea. Taxa recorded in Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, and Thyrididae are also included. Moth taxa were collected at ultraviolet lights, bait, introduced Bahiagrass (Paspalum notatum), and by netting specimens. A list of taxa recorded feeding on P. notatum is presented. Introduction The University of Florida Natural Area Teaching Laboratory (NATL) contains 40 acres of natural habitats maintained for scientific research, conservation, and teaching purposes. Habitat types present include hammock, upland pine, disturbed open field, cat tail marsh, and shallow pond. An active management plan has been developed for this area, including prescribed burning to restore the upland pine community and establishment of plots to study succession (http://csssrvr.entnem.ufl.edu/~walker/natl.htm). The site is a popular collecting locality for student and scientific collections. The author has done extensive collecting and field work at NATL, and two previous reports have resulted from this work, including: a biodiversity inventory of the butterflies (Lepidoptera: Hesperioidea & Papilionoidea) of NATL (Kons 1999), and an ecological study of Hermeuptychia hermes (F.) and Megisto cymela (Cram.) in NATL habitats (Kons 1998). Other workers have posted NATL check lists for Ichneumonidae, Sphecidae, Tettigoniidae, and Gryllidae (http://csssrvr.entnem.ufl.edu/~walker/insect.htm).
    [Show full text]
  • Effect of Different Mowing Regimes on Butterflies and Diurnal Moths on Road Verges A
    Animal Biodiversity and Conservation 29.2 (2006) 133 Effect of different mowing regimes on butterflies and diurnal moths on road verges A. Valtonen, K. Saarinen & J. Jantunen Valtonen, A., Saarinen, K. & Jantunen, J., 2006. Effect of different mowing regimes on butterflies and diurnal moths on road verges. Animal Biodiversity and Conservation, 29.2: 133–148. Abstract Effect of different mowing regimes on butterflies and diurnal moths on road verges.— In northern and central Europe road verges offer alternative habitats for declining plant and invertebrate species of semi– natural grasslands. The quality of road verges as habitats depends on several factors, of which the mowing regime is one of the easiest to modify. In this study we compared the Lepidoptera communities on road verges that underwent three different mowing regimes regarding the timing and intensity of mowing; mowing in mid–summer, mowing in late summer, and partial mowing (a narrow strip next to the road). A total of 12,174 individuals and 107 species of Lepidoptera were recorded. The mid–summer mown verges had lower species richness and abundance of butterflies and lower species richness and diversity of diurnal moths compared to the late summer and partially mown verges. By delaying the annual mowing until late summer or promoting mosaic–like mowing regimes, such as partial mowing, the quality of road verges as habitats for butterflies and diurnal moths can be improved. Key words: Mowing management, Road verge, Butterfly, Diurnal moth, Alternative habitat, Mowing intensity. Resumen Efecto de los distintos regímenes de siega de los márgenes de las carreteras sobre las polillas diurnas y las mariposas.— En Europa central y septentrional los márgenes de las carreteras constituyen hábitats alternativos para especies de invertebrados y plantas de los prados semi–naturales cuyas poblaciones se están reduciendo.
    [Show full text]
  • Check List of Noctuid Moths (Lepidoptera: Noctuidae And
    Бiологiчний вiсник МДПУ імені Богдана Хмельницького 6 (2), стор. 87–97, 2016 Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University, 6 (2), pp. 87–97, 2016 ARTICLE UDC 595.786 CHECK LIST OF NOCTUID MOTHS (LEPIDOPTERA: NOCTUIDAE AND EREBIDAE EXCLUDING LYMANTRIINAE AND ARCTIINAE) FROM THE SAUR MOUNTAINS (EAST KAZAKHSTAN AND NORTH-EAST CHINA) A.V. Volynkin1, 2, S.V. Titov3, M. Černila4 1 Altai State University, South Siberian Botanical Garden, Lenina pr. 61, Barnaul, 656049, Russia. E-mail: [email protected] 2 Tomsk State University, Laboratory of Biodiversity and Ecology, Lenina pr. 36, 634050, Tomsk, Russia 3 The Research Centre for Environmental ‘Monitoring’, S. Toraighyrov Pavlodar State University, Lomova str. 64, KZ-140008, Pavlodar, Kazakhstan. E-mail: [email protected] 4 The Slovenian Museum of Natural History, Prešernova 20, SI-1001, Ljubljana, Slovenia. E-mail: [email protected] The paper contains data on the fauna of the Lepidoptera families Erebidae (excluding subfamilies Lymantriinae and Arctiinae) and Noctuidae of the Saur Mountains (East Kazakhstan). The check list includes 216 species. The map of collecting localities is presented. Key words: Lepidoptera, Noctuidae, Erebidae, Asia, Kazakhstan, Saur, fauna. INTRODUCTION The fauna of noctuoid moths (the families Erebidae and Noctuidae) of Kazakhstan is still poorly studied. Only the fauna of West Kazakhstan has been studied satisfactorily (Gorbunov 2011). On the faunas of other parts of the country, only fragmentary data are published (Lederer, 1853; 1855; Aibasov & Zhdanko 1982; Hacker & Peks 1990; Lehmann et al. 1998; Benedek & Bálint 2009; 2013; Korb 2013). In contrast to the West Kazakhstan, the fauna of noctuid moths of East Kazakhstan was studied inadequately.
    [Show full text]
  • MOTHS and BUTTERFLIES LEPIDOPTERA DISTRIBUTION DATA SOURCES (LEPIDOPTERA) * Detailed Distributional Information Has Been J.D
    MOTHS AND BUTTERFLIES LEPIDOPTERA DISTRIBUTION DATA SOURCES (LEPIDOPTERA) * Detailed distributional information has been J.D. Lafontaine published for only a few groups of Lepidoptera in western Biological Resources Program, Agriculture and Agri-food Canada. Scott (1986) gives good distribution maps for Canada butterflies in North America but these are generalized shade Central Experimental Farm Ottawa, Ontario K1A 0C6 maps that give no detail within the Montane Cordillera Ecozone. A series of memoirs on the Inchworms (family and Geometridae) of Canada by McGuffin (1967, 1972, 1977, 1981, 1987) and Bolte (1990) cover about 3/4 of the Canadian J.T. Troubridge fauna and include dot maps for most species. A long term project on the “Forest Lepidoptera of Canada” resulted in a Pacific Agri-Food Research Centre (Agassiz) four volume series on Lepidoptera that feed on trees in Agriculture and Agri-Food Canada Canada and these also give dot maps for most species Box 1000, Agassiz, B.C. V0M 1A0 (McGugan, 1958; Prentice, 1962, 1963, 1965). Dot maps for three groups of Cutworm Moths (Family Noctuidae): the subfamily Plusiinae (Lafontaine and Poole, 1991), the subfamilies Cuculliinae and Psaphidinae (Poole, 1995), and ABSTRACT the tribe Noctuini (subfamily Noctuinae) (Lafontaine, 1998) have also been published. Most fascicles in The Moths of The Montane Cordillera Ecozone of British Columbia America North of Mexico series (e.g. Ferguson, 1971-72, and southwestern Alberta supports a diverse fauna with over 1978; Franclemont, 1973; Hodges, 1971, 1986; Lafontaine, 2,000 species of butterflies and moths (Order Lepidoptera) 1987; Munroe, 1972-74, 1976; Neunzig, 1986, 1990, 1997) recorded to date.
    [Show full text]
  • Project Noah National Moth Week 2013 Data
    PROJECT NOAH NATIONAL MOTH WEEK 2013 DATA Following the immense success of Project Noah’s collaboration with National Moth Week during the event’s first year, Project Noah participated in the second annual National Moth Week, which occurred from July 20, 2013 to July 28, 2013. Project Noah surpassed its goal of one-thousand moths spotted during National Moth Week with 1347 moths spotted. Spottings were submitted to Project Noah’s Moths of the World mission. Data organization and presentation by Jacob Gorneau. Project Noah National Moth Week 2013 Data | Jacob Gorneau 1 Moths of the World Mission for National Moth Week July 20, 2013 to July 28, 2013 Number Of Spottings Total 1347 Total Unidentified 480 Total Identified 867 Africa 55 Mozambique 1 South Africa 54 Asia 129 Bhutan 47 China 1 India 33 Indonesia 7 Japan 2 Malaysia 3 Philippines 17 Sri Lanka 7 Thailand 10 Turkey 2 Australia 22 Australia 21 New Zealand 1 Europe 209 Belgium 1 Bosnia and Herzegovina 5 Croatia 13 Denmark 66 Project Noah National Moth Week 2013 Data | Jacob Gorneau 2 France 1 Georgia 1 Germany 23 Greece 5 Italy 1 Netherlands 21 Norway 2 Portugal 6 Slovakia 11 Spain 38 Switzerland 1 United Kingdom 14 North America 926 Canada 54 Costa Rica 15 Mexico 84 United States of America 773 South America 6 Brazil 2 Chile 4 Total 7/20/2013 164 Total 7/21/2013 149 Total 7/22/2013 100 Total 7/23/2013 144 Total 7/24/2013 134 Total 7/25/2013 130 Total 7/26/2013 105 Total 7/27/2013 240 Total 7/28/2013 181 Project Noah National Moth Week 2013 Data | Jacob Gorneau 3 Continent/Country/Species Spottings Africa 55 Mozambique 1 Egybolis vaillantina 1 South Africa 54 Agdistis sp.
    [Show full text]
  • CHECKLIST of WISCONSIN MOTHS (Superfamilies Mimallonoidea, Drepanoidea, Lasiocampoidea, Bombycoidea, Geometroidea, and Noctuoidea)
    WISCONSIN ENTOMOLOGICAL SOCIETY SPECIAL PUBLICATION No. 6 JUNE 2018 CHECKLIST OF WISCONSIN MOTHS (Superfamilies Mimallonoidea, Drepanoidea, Lasiocampoidea, Bombycoidea, Geometroidea, and Noctuoidea) Leslie A. Ferge,1 George J. Balogh2 and Kyle E. Johnson3 ABSTRACT A total of 1284 species representing the thirteen families comprising the present checklist have been documented in Wisconsin, including 293 species of Geometridae, 252 species of Erebidae and 584 species of Noctuidae. Distributions are summarized using the six major natural divisions of Wisconsin; adult flight periods and statuses within the state are also reported. Examples of Wisconsin’s diverse native habitat types in each of the natural divisions have been systematically inventoried, and species associated with specialized habitats such as peatland, prairie, barrens and dunes are listed. INTRODUCTION This list is an updated version of the Wisconsin moth checklist by Ferge & Balogh (2000). A considerable amount of new information from has been accumulated in the 18 years since that initial publication. Over sixty species have been added, bringing the total to 1284 in the thirteen families comprising this checklist. These families are estimated to comprise approximately one-half of the state’s total moth fauna. Historical records of Wisconsin moths are relatively meager. Checklists including Wisconsin moths were compiled by Hoy (1883), Rauterberg (1900), Fernekes (1906) and Muttkowski (1907). Hoy's list was restricted to Racine County, the others to Milwaukee County. Records from these publications are of historical interest, but unfortunately few verifiable voucher specimens exist. Unverifiable identifications and minimal label data associated with older museum specimens limit the usefulness of this information. Covell (1970) compiled records of 222 Geometridae species, based on his examination of specimens representing at least 30 counties.
    [Show full text]