Merrimac Farm WMA Insect List As of September 2014 Order Family
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Celtis Tenuifolia) in Ontario
Photo: Allen Woodliffe Dwarf Hackberry (Celtis tenuifolia) in Ontario Ontario Recovery Strategy Series Recovery strategy prepared under the Endangered Species Act, 2007 2013 Ministry of Natural Resources About the Ontario Recovery Strategy Series This series presents the collection of recovery strategies that are prepared or adopted as advice to the Province of Ontario on the recommended approach to recover species at risk. The Province ensures the preparation of recovery strategies to meet its commitments to recover species at risk under the Endangered Species Act (ESA) and the Accord for the Protection of Species at Risk in Canada. What is recovery? What’s next? Recovery of species at risk is the process by which the Nine months after the completion of a recovery strategy decline of an endangered, threatened, or extirpated a government response statement will be published species is arrested or reversed, and threats are which summarizes the actions that the Government of removed or reduced to improve the likelihood of a Ontario intends to take in response to the strategy. species’ persistence in the wild. The implementation of recovery strategies depends on the continued cooperation and actions of government agencies, individuals, communities, land users, and What is a recovery strategy? conservationists. Under the ESA a recovery strategy provides the best available scientific knowledge on what is required to For more information achieve recovery of a species. A recovery strategy outlines the habitat needs and the threats to the To learn more about species at risk recovery in Ontario, survival and recovery of the species. It also makes please visit the Ministry of Natural Resources Species at recommendations on the objectives for protection and Risk webpage at: www.ontario.ca/speciesatrisk recovery, the approaches to achieve those objectives, and the area that should be considered in the development of a habitat regulation. -
Caterpillars Moths Butterflies Woodies
NATIVE Caterpillars Moths and utter flies Band host NATIVE Hackberry Emperor oodies PHOTO : Megan McCarty W Double-toothed Prominent Honey locust Moth caterpillar Hackberry Emperor larva PHOTO : Douglas Tallamy Big Poplar Sphinx Number of species of Caterpillars n a study published in 2009, Dr. Oaks (Quercus) 557 Beeches (Fagus) 127 Honey-locusts (Gleditsia) 46 Magnolias (Magnolia) 21 Double-toothed Prominent ( Nerice IDouglas W. Tallamy, Ph.D, chair of the Cherries (Prunus) 456 Serviceberry (Amelanchier) 124 New Jersey Tea (Ceanothus) 45 Buttonbush (Cephalanthus) 19 bidentata ) larvae feed exclusively on elms Department of Entomology and Wildlife Willows (Salix) 455 Larches or Tamaracks (Larix) 121 Sycamores (Platanus) 45 Redbuds (Cercis) 19 (Ulmus), and can be found June through Ecology at the University of Delaware Birches (Betula) 411 Dogwoods (Cornus) 118 Huckleberry (Gaylussacia) 44 Green-briar (Smilax) 19 October. Their body shape mimics the specifically addressed the usefulness of Poplars (Populus) 367 Firs (Abies) 117 Hackberry (Celtis) 43 Wisterias (Wisteria) 19 toothed shape of American elm, making native woodies as host plants for our Crabapples (Malus) 308 Bayberries (Myrica) 108 Junipers (Juniperus) 42 Redbay (native) (Persea) 18 them hard to spot. The adult moth is native caterpillars (and obviously Maples (Acer) 297 Viburnums (Viburnum) 104 Elders (Sambucus) 42 Bearberry (Arctostaphylos) 17 small with a wingspan of 3-4 cm. therefore moths and butterflies). Blueberries (Vaccinium) 294 Currants (Ribes) 99 Ninebark (Physocarpus) 41 Bald cypresses (Taxodium) 16 We present here a partial list, and the Alders (Alnus) 255 Hop Hornbeam (Ostrya) 94 Lilacs (Syringa) 40 Leatherleaf (Chamaedaphne) 15 Honey locust caterpillar feeds on honey number of Lepidopteran species that rely Hickories (Carya) 235 Hemlocks (Tsuga) 92 Hollies (Ilex) 39 Poison Ivy (Toxicodendron) 15 locust, and Kentucky coffee trees. -
New Moths from Texas (Noctuidae, Tortricidae)
1968 Joltrnal of the Lepidopterists' Societu 133 NEW MOTHS FROM TEXAS (NOCTUIDAE, TORTRICIDAE) ANDRE BLANCHARD 3023 Underwood, Houston, Texas As a retirement hobby, I decided, six years ago, to catalog the moths of Texas. My wife and I have been collecting moths all over Texas for the last four years. As the work progressed, I came to realize that I may have to settle, more modestly, for a "Contributions Toward A Catalog of the Moths of Texas." The number of species in my collection which had apparently never been taken in Texas is quite large, and the number of those which seem to be new to science, particularly from the mountain ranges and desert areas of West Texas, is much larger than I ever expected. I have been fortunate in interesting several specialists in describing some of these new species: Dr. C. L. Hogue (196S), Mr. McElvare ( 1966), Dr. E. L. Todd (1966) have described three. Difficult cases are now and, in the future, will be submitted to experts. I have de scribed the male of a fourth species (1966), the female of which was described by Dr. F. H. Hindge (1966). While getting more material for my intcnded catalog, I shall describe as many of the new species as I can name without becoming guilty of adding to the confusion which already exists in some genera. In the present paper, I describe six new noctuids and one tortricid species. All types were collected by A. &. M. E. Blanchard. Acronicta vallis cola Blanchard, new species (PI. I, fig. J; PI. -
Alternative Transmission Patterns in Independently Acquired Nutritional Co-Symbionts of Dictyopharidae Planthoppers
bioRxiv preprint doi: https://doi.org/10.1101/2021.04.07.438848; this version posted April 9, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Alternative transmission patterns in independently acquired nutritional co-symbionts of Dictyopharidae planthoppers Anna Michalik1*, Diego C. Franco2, Michał Kobiałka1, Teresa Szklarzewicz1, Adam Stroiński3, Piotr Łukasik2 1Department of Developmental Biology and Morphology of Invertebrates, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Gronostajowa 9, 30-387 Kraków, Poland 2Institute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland 3Museum and Institute of Zoology, Polish Academy of Sciences, Wilcza 64, 00-679 Warszawa, Poland Abstract Keywords: planthoppers, nutritional endosymbiosis, Sap-sucking hemipterans host specialized, heritable transovarial transmission microorganisms that supplement their unbalanced diet with essential nutrients. These microbes show unusual features Significance statement that provide a unique perspective on the evolution of life but Sup-sucking hemipterans host ancient heritable have not been systematically studied. Here, we combine microorganisms that supplement their unbalanced diet with microscopy with high-throughput sequencing to revisit 80- essential nutrients, and which have repeatedly been year-old reports on the diversity of symbiont transmission complemented or replaced by other microorganisms. They modes in a broadly distributed planthopper family need to be reliably transmitted to subsequent generations Dictyopharidae. We show that in all species examined, the through the reproductive system, and often they end up using ancestral nutritional endosymbionts Sulcia and Vidania are the same route as the ancient symbionts. -
Checklist of the Coleoptera of New Brunswick, Canada
A peer-reviewed open-access journal ZooKeys 573: 387–512 (2016)Checklist of the Coleoptera of New Brunswick, Canada 387 doi: 10.3897/zookeys.573.8022 CHECKLIST http://zookeys.pensoft.net Launched to accelerate biodiversity research Checklist of the Coleoptera of New Brunswick, Canada Reginald P. Webster1 1 24 Mill Stream Drive, Charters Settlement, NB, Canada E3C 1X1 Corresponding author: Reginald P. Webster ([email protected]) Academic editor: P. Bouchard | Received 3 February 2016 | Accepted 29 February 2016 | Published 24 March 2016 http://zoobank.org/34473062-17C2-4122-8109-3F4D47BB5699 Citation: Webster RP (2016) Checklist of the Coleoptera of New Brunswick, Canada. In: Webster RP, Bouchard P, Klimaszewski J (Eds) The Coleoptera of New Brunswick and Canada: providing baseline biodiversity and natural history data. ZooKeys 573: 387–512. doi: 10.3897/zookeys.573.8022 Abstract All 3,062 species of Coleoptera from 92 families known to occur in New Brunswick, Canada, are re- corded, along with their author(s) and year of publication using the most recent classification framework. Adventive and Holarctic species are indicated. There are 366 adventive species in the province, 12.0% of the total fauna. Keywords Checklist, Coleoptera, New Brunswick, Canada Introduction The first checklist of the beetles of Canada by Bousquet (1991) listed 1,365 species from the province of New Brunswick, Canada. Since that publication, many species have been added to the faunal list of the province, primarily from increased collection efforts and -
Swede's Forest SNA Bioblitz Results
Swede Forest SNA Bioblitz Findings Species found at the June 17, 2017 bioblitz. Bacteria: Birds: • Apical chlorosis of Canada thistle aka PST – • Ring-necked Pheasant (Phasianus colchicus) (Pseudomonas syringae pv. tagetis) • Pied-billed Grebe (Podilymbus podiceps) Fungi and Lichens: • American White Pelican (Pelecanus erythrorhynchos) • Crown Rust (Puccinia coronata) • Green Heron (Butorides virescens) Amphibians: • Killdeer (Charadrius vociferus) • Mourning Dove (Zenaida macroura) • Northern Leopard Frog (Rana pipiens) • Turkey Vulture (Cathartes aura) • Eastern Gray Treefrog (Hyla versicolor) • Bald Eagle (Haliaeetus leucocephalus) • Belted Kingfisher (Megaceryle alcyon) Reptiles: • Eastern Kingbird (Tyrannus tyrannus) • Red-sided Garter Snake (Thamnophis sirtalis • Great Crested Flycatcher (Myiarchus crinitus) parietalis) • Eastern Wood-Pewee (Contopus virens) • Plains Garter Snake (Thamnophis radix) • Brown-headed Cowbird (Molothrus ater) • Redbelly Snake (Storeria occipitomaculata) • Red-winged Blackbird (Agelaius phoeniceus) • Five-lined Skink (Plestiodon fasciatus) • Orchard Oriole (Icterus spurius) • Western Painted Turtle (Chrysemys picta belli) • Baltimore Oriole (Icterus galbula) • Common Grackle (Quiscalus quiscula) Mammals: • American Goldfinch (Spinus tristis) • Eastern Cottontail (Sylvilagus floridanus) • Lark Sparrow (Chondestes grammacus)— • Whitetail Deer (Odocoileus virginianus) confirmed nesting • White-footed Mouse (Peromyscus leucopus) • Chipping Sparrow (Spizella passerina) • Coyote (Canis latrans) scat • Clay-colored -
1 Appendix 3. Thousand Islands National Park Taxonomy Report
Appendix 3. Thousand Islands National Park Taxonomy Report Class Order Family Genus Species Arachnida Araneae Agelenidae Agelenopsis Agelenopsis potteri Agelenopsis utahana Anyphaenidae Anyphaena Anyphaena celer Hibana Hibana gracilis Araneidae Araneus Araneus bicentenarius Larinioides Larinioides cornutus Larinioides patagiatus Clubionidae Clubiona Clubiona abboti Clubiona bishopi Clubiona canadensis Clubiona kastoni Clubiona obesa Clubiona pygmaea Elaver Elaver excepta Corinnidae Castianeira Castianeira cingulata Phrurolithus Phrurolithus festivus Dictynidae Emblyna Emblyna cruciata Emblyna sublata Eutichuridae Strotarchus Strotarchus piscatorius Gnaphosidae Herpyllus Herpyllus ecclesiasticus Zelotes Zelotes hentzi Linyphiidae Ceraticelus Ceraticelus atriceps 1 Collinsia Collinsia plumosa Erigone Erigone atra Hypselistes Hypselistes florens Microlinyphia Microlinyphia mandibulata Neriene Neriene radiata Soulgas Soulgas corticarius Spirembolus Lycosidae Pardosa Pardosa milvina Pardosa moesta Piratula Piratula canadensis Mimetidae Mimetus Mimetus notius Philodromidae Philodromus Philodromus peninsulanus Philodromus rufus vibrans Philodromus validus Philodromus vulgaris Thanatus Thanatus striatus Phrurolithidae Phrurotimpus Phrurotimpus borealis Pisauridae Dolomedes Dolomedes tenebrosus Dolomedes triton Pisaurina Pisaurina mira Salticidae Eris Eris militaris Hentzia Hentzia mitrata Naphrys Naphrys pulex Pelegrina Pelegrina proterva Tetragnathidae Tetragnatha 2 Tetragnatha caudata Tetragnatha shoshone Tetragnatha straminea Tetragnatha viridis -
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, -
Natural Communities of Michigan: Classification and Description
Natural Communities of Michigan: Classification and Description Prepared by: Michael A. Kost, Dennis A. Albert, Joshua G. Cohen, Bradford S. Slaughter, Rebecca K. Schillo, Christopher R. Weber, and Kim A. Chapman Michigan Natural Features Inventory P.O. Box 13036 Lansing, MI 48901-3036 For: Michigan Department of Natural Resources Wildlife Division and Forest, Mineral and Fire Management Division September 30, 2007 Report Number 2007-21 Version 1.2 Last Updated: July 9, 2010 Suggested Citation: Kost, M.A., D.A. Albert, J.G. Cohen, B.S. Slaughter, R.K. Schillo, C.R. Weber, and K.A. Chapman. 2007. Natural Communities of Michigan: Classification and Description. Michigan Natural Features Inventory, Report Number 2007-21, Lansing, MI. 314 pp. Copyright 2007 Michigan State University Board of Trustees. Michigan State University Extension programs and materials are open to all without regard to race, color, national origin, gender, religion, age, disability, political beliefs, sexual orientation, marital status or family status. Cover photos: Top left, Dry Sand Prairie at Indian Lake, Newaygo County (M. Kost); top right, Limestone Bedrock Lakeshore, Summer Island, Delta County (J. Cohen); lower left, Muskeg, Luce County (J. Cohen); and lower right, Mesic Northern Forest as a matrix natural community, Porcupine Mountains Wilderness State Park, Ontonagon County (M. Kost). Acknowledgements We thank the Michigan Department of Natural Resources Wildlife Division and Forest, Mineral, and Fire Management Division for funding this effort to classify and describe the natural communities of Michigan. This work relied heavily on data collected by many present and former Michigan Natural Features Inventory (MNFI) field scientists and collaborators, including members of the Michigan Natural Areas Council. -
The Influence of Prairie Restoration on Hemiptera
CAN THE ONE TRUE BUG BE THE ONE TRUE ANSWER? THE INFLUENCE OF PRAIRIE RESTORATION ON HEMIPTERA COMPOSITION Thesis Submitted to The College of Arts and Sciences of the UNIVERSITY OF DAYTON In Partial Fulfillment of the Requirements for The Degree of Master of Science in Biology By Stephanie Kay Gunter, B.A. Dayton, Ohio August 2021 CAN THE ONE TRUE BUG BE THE ONE TRUE ANSWER? THE INFLUENCE OF PRAIRIE RESTORATION ON HEMIPTERA COMPOSITION Name: Gunter, Stephanie Kay APPROVED BY: Chelse M. Prather, Ph.D. Faculty Advisor Associate Professor Department of Biology Ryan W. McEwan, Ph.D. Committee Member Associate Professor Department of Biology Mark G. Nielsen Ph.D. Committee Member Associate Professor Department of Biology ii © Copyright by Stephanie Kay Gunter All rights reserved 2021 iii ABSTRACT CAN THE ONE TRUE BUG BE THE ONE TRUE ANSWER? THE INFLUENCE OF PRAIRIE RESTORATION ON HEMIPTERA COMPOSITION Name: Gunter, Stephanie Kay University of Dayton Advisor: Dr. Chelse M. Prather Ohio historically hosted a patchwork of tallgrass prairies, which provided habitat for native species and prevented erosion. As these vulnerable habitats have declined in the last 200 years due to increased human land use, restorations of these ecosystems have increased, and it is important to evaluate their success. The Hemiptera (true bugs) are an abundant and varied order of insects including leafhoppers, aphids, cicadas, stink bugs, and more. They play important roles in grassland ecosystems, feeding on plant sap and providing prey to predators. Hemipteran abundance and composition can respond to grassland restorations, age of restoration, and size and isolation of habitat. -
Journal of the Lepidopterists' Society
JOURNAL OF THE LEPIDOPTERISTS' SOCIETY Volume 38 1984 Number 3 Joumal of the Lepidopterists' Society 38(3). 1984. 149-164 SOD WEBWORM MOTHS (PYRALIDAE: CRAMBINAE) IN SOUTH DAKOTA B. McDANIEL,l G. FAUSKEl AND R. D. GUSTIN 2 ABSTRACT. Twenty-seven species of the subfamily Crambinae known as sod web worm moths were collected from South Dakota. A key to species has been included as well as their distribution patterns in South Dakota. This study began after damage to rangeland in several South Dakota counties in the years 1974 and 1975. Damage was reported from Cor son, Dewey, Harding, Haakon, Meade, Perkins, Stanley and Ziebach counties. An effort was made to determine the species of Crambinae present in South Dakota and their distribution. Included are a key for species identification and a list of species with their flight periods and collection sites. MATERIALS AND METHODS Black light traps using the General Electric Fluorescent F ls T8 B1 15 watt bulb were set up in Brookings, Jackson, Lawrence, Minnehaha, Pennington and Spink counties. In Minnehaha County collecting was carried out with a General Electric 200 watt soft-glow bulb. Daytime collecting was used in several localities. Material in the South Dakota State University Collection was also utilized. For each species a map is included showing collection localities by county. On the maps the following symbols are used: • = collected by sweepnet. Q = collected by light trap. Key to South Dakota Cram binae 1a. Rs stalked .__ ... ___ .. __ ......................... _..... _ ................................. _._............................................. 2 lb. Rs arising directly from discal cell ................................................................. _............ _............ -
DNA Barcoding and Morphology Reveal Three Cryptic Species of Anania
Systematic Entomology (2012), 37, 686–705 DNA barcoding and morphology reveal three cryptic species of Anania (Lepidoptera: Crambidae: Pyraustinae) in North America, all distinct from their European counterpart ZHAOFU YANG1,9, JEAN-FRANC¸ OIS LANDRY2,LOUIS HANDFIELD3, YALIN ZHANG1,M.ALMASOLIS4, DANIEL HANDFIELD5, BRIAN G. SCHOLTENS6, MARKO MUTANEN7, MATTHIAS NUSS8 and PAUL D. N. HEBERT9 1Key laboratory of Plant Protection Resources and Pest Management, Ministry of Education; Entomological Museum, Northwest A&F University, Yangling, China, 2Agriculture and Agri-Food Canada, Eastern Cereal and Oilseed Research Centre, C.E.F., Ottawa, Ontario K1A 0C6, Canada, 3133 rue Messier, #301, Mont-Saint-Hilaire, Quebec´ J3H 2W8, Canada, 4Systematic Entomology Laboratory, USDA, c/o Smithsonian Institution, National Museum Natural History, Washington, DC 20013-7012, U.S.A., 5Chemin des Grands Coteaux, Saint-Mathieu-de-Beloeil, Quebec,´ Canada, 6Department of Biology, College of Charleston, SC, U.S.A., 7Department of Biology, University of Oulu, Zoological Museum, Oulu, Finland, 8Museum of Zoology, Senckenberg Natural History Collections Dresden, Konigsbr¨ ucker¨ Landstrasse 159, 01109 Dresden, Germany and 9Biodiversity Institute of Ontario, University of Guelph, Guelph, Ontario N1G 2W1, Canada Abstract. Anania coronata (Hufnagel), a Holarctic species of pyraustine crambid moth, has long been treated as having two geographically separated subspecies – the nominotypical Anania coronata in the Palaearctic Region and Anania coronata tertialis (Guenee)´ in the Nearctic Region. Maximum likelihood and Bayesian inference analysis of mitochondrial DNA barcodes both recover four well-supported, reciprocally monophyletic groups within Anania coronata. Qualitative and quantitative analyses of genital structures reveal diagnostic differences that correspond to the four barcode lineages. On the basis of both molecular and morphological evidence, we conclude that Anania coronata is actually a complex of four species.