Its Natural History
Total Page:16
File Type:pdf, Size:1020Kb
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, -
Tree Swallows (Tachycineta Bicolor) Nesting on Wetlands Impacted by Oil Sands Mining Are Highly Parasitized by the Bird Blow Fly Protocalliphora Spp
Journal of Wildlife Diseases, 43(2), 2007, pp. 167–178 # Wildlife Disease Association 2007 TREE SWALLOWS (TACHYCINETA BICOLOR) NESTING ON WETLANDS IMPACTED BY OIL SANDS MINING ARE HIGHLY PARASITIZED BY THE BIRD BLOW FLY PROTOCALLIPHORA SPP. Marie-Line Gentes,1 Terry L. Whitworth,2 Cheryl Waldner,3 Heather Fenton,1 and Judit E. Smits1,4 1 Department of Veterinary Pathology, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5B4, Canada 2 Whitworth Pest Solutions, Inc., 2533 Inter Avenue, Puyallup, Washington, USA 3 Department of Large Animal Clinical Sciences, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5B4, Canada 4 Corresponding author (email: [email protected]) ABSTRACT: Oil sands mining is steadily expanding in Alberta, Canada. Major companies are planning reclamation strategies for mine tailings, in which wetlands will be used for the bioremediation of water and sediments contaminated with polycyclic aromatic hydrocarbons and naphthenic acids during the extraction process. A series of experimental wetlands were built on companies’ leases to assess the feasibility of this approach, and tree swallows (Tachycineta bicolor) were designated as upper trophic biological sentinels. From May to July 2004, prevalence and intensity of infestation with bird blow flies Protocalliphora spp. (Diptera: Calliphoridae) were measured in nests on oil sands reclaimed wetlands and compared with those on a reference site. Nestling growth and survival also were monitored. Prevalence of infestation was surprisingly high for a small cavity nester; 100% of the 38 nests examined were infested. Nests on wetlands containing oil sands waste materials harbored on average from 60% to 72% more blow fly larvae than those on the reference site. -
DNA Barcoding Cannot Reliably Identify Species of the Blowfly Genus Protocalliphora (Diptera: Calliphoridae)
DNA barcoding cannot reliably identify species of the blowfly genus Protocalliphora (Diptera: Calliphoridae). T. L. Whitworth, R. D. Dawson, Hélène Magalon, E. Baudry To cite this version: T. L. Whitworth, R. D. Dawson, Hélène Magalon, E. Baudry. DNA barcoding cannot reli- ably identify species of the blowfly genus Protocalliphora (Diptera: Calliphoridae).. Proceedings of the Royal Society B: Biological Sciences, Royal Society, The, 2007, 274 (1619), pp.1731-1739. 10.1098/rspb.2007.0062. hal-00941689 HAL Id: hal-00941689 https://hal.archives-ouvertes.fr/hal-00941689 Submitted on 6 May 2016 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. DNA barcoding cannot reliably identify species of the blowfly genus Protocalliphora (Diptera: Calliphoridae) T. L. Whitworth1, R. D. Dawson2, H. Magalon3 and E. Baudry4,* 1Washington State University, 2533 Inter Avenue, Puyallup, WA 98372, USA 2University of Northern British Columbia, Prince George, British Columbia V2N 4Z9, Canada 3Laboratoire d’Ecologie, Universite´ Paris VI, Paris 75252, France 4Laboratoire Ecologie, Systematique et Evolution, Universite´ Paris-Sud, Baˆtiment 362, 91405 Orsay Cedex, France In DNA barcoding, a short standardized DNA sequence is used to assign unknown individuals to species and aid in the discovery of new species. -
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. -
Host–Parasite Relationships and Co-Infection of Nasal Mites of Chrysomus Ruficapillus (Passeriformes: Icteridae) in Southern Brazil
Iheringia Série Zoologia Museu de Ciências Naturais e-ISSN 1678-4766 www.scielo.br/isz Fundação Zoobotânica do Rio Grande do Sul Host–Parasite relationships and co-infection of nasal mites of Chrysomus ruficapillus (Passeriformes: Icteridae) in southern Brazil Fabiana Fedatto Bernardon1 , Carolina S. Mascarenhas1 , Joaber Pereira Jr2 & Gertrud Müller1 1. Laboratório de Parasitologia de Animais Silvestres (LAPASIL), Departamento de Microbiologia e Parasitologia, Instituto de Biologia, Universidade Federal de Pelotas, Caixa Postal 354, 96010-900, Pelotas, RS, Brazil. ([email protected]) 2. Laboratório de Biologia de Parasitos de Organismos Aquáticos (LABPOA), Instituto de Oceanografia, Universidade Federal do Rio Grande, Caixa Postal 474, 96650-900 Rio Grande, Rio Grande do Sul, Brazil Received 14 December 2017 Accepted 8 May 2018 Published 21 June 2018 DOI: 10.1590/1678-4766e2018025 ABSTRACT. One hundred twenty-two Chrysomus ruficapillus were examined in southern Brazil, in order to research the presence of nasal mites and the parasite-host relationships. Nasal mite infections were analyzed for: presence of Ereynetidae and Rhinonyssidae considering the total number of hosts examined; Sexual maturity of males (juveniles and adults); Periods of bird collection and presence of co-infections. Were identified five taxa, four belongs to Rhinonyssidae (Sternostoma strandtmanni, Ptilonyssus sairae, P. icteridius and Ptilonyssus sp.) and one to Ereynetidae (Boydaia agelaii). Adult males were parasitized for one taxa more than juvenile males. Co-infections occurred in 22 hosts, between two, three and four taxa, belonging to Ereynetidae and Rhinonyssidae.The co-infections were more prevalent in austral autumn / winter. The host-parasite relations and co-infections by nasal mites in C. -
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. -
Diptera: Calliphoridae) T
Proc. R. Soc. B (2007) 274, 1731–1739 doi:10.1098/rspb.2007.0062 Published online 1 May 2007 DNA barcoding cannot reliably identify species of the blowfly genus Protocalliphora (Diptera: Calliphoridae) T. L. Whitworth1, R. D. Dawson2, H. Magalon3 and E. Baudry4,* 1Washington State University, 2533 Inter Avenue, Puyallup, WA 98372, USA 2University of Northern British Columbia, Prince George, British Columbia V2N 4Z9, Canada 3Laboratoire d’Ecologie, Universite´ Paris VI, Paris 75252, France 4Laboratoire Ecologie, Systematique et Evolution, Universite´ Paris-Sud, Baˆtiment 362, 91405 Orsay Cedex, France In DNA barcoding, a short standardized DNA sequence is used to assign unknown individuals to species and aid in the discovery of new species. A fragment of the mitochondrial gene cytochrome c oxidase subunit 1 is emerging as the standard barcode region for animals. However, patterns of mitochondrial variability can be confounded by the spread of maternally transmitted bacteria that cosegregate with mitochondria. Here, we investigated the performance of barcoding in a sample comprising 12 species of the blow fly genus Protocalliphora, known to be infected with the endosymbiotic bacteria Wolbachia.We found that the barcoding approach showed very limited success: assignment of unknown individuals to species is impossible for 60% of the species, while using the technique to identify new species would underestimate the species number in the genus by 75%. This very low success of the barcoding approach is due to the non-monophyly of many of the species at the mitochondrial level. We even observed individuals from four different species with identical barcodes, which is, to our knowledge, the most extensive case of mtDNA haplotype sharing yet described. -
Assabet River National Wildlife Refuge Final Comprehensive Conservation Plan January 2005
U.S. Fish & Wildlife Service Assabet River National Wildlife Refuge Final Comprehensive Conservation Plan January 2005 This goose, designed by J.N. “Ding” Darling, has become the symbol of the National Wildlife Refuge System The U.S. Fish and Wildlife Service is the principle federal agency for conserving, protecting, and enhancing fish and wildlife in their habitats for the continuing benefit of the American people. The Service manages the 96-million acre National Wildlife Refuge System comprised of 544 national wildlife refuges and thousands of waterfowl production areas. It also operates 65 national fish hatcheries and 78 ecological services field stations. The agency enforces federal wildlife laws, manages migratory bird populations, restores significant fisheries, conserves and restores wildlife habitat such as wetlands, administers the Endangered Species Act, and helps foreign governments with their conservation efforts. It also oversees the Federal Aid program which distributes hundreds of millions of dollars in excise taxes on fishing and hunting equipment to state wildlife agencies. Comprehensive Conservation Plans provide long term guidance for management decisions; set forth goals, objectives, and strategies needed to accomplish refuge purposes; and, identify the Service’s best estimate of future needs. These plans detail program planning levels that are sometimes substantially above current budget allocations and, as such, are primarily for Service strategic planning and program prioritization purposes. The plans do not constitute -
Rhinonyssidae (Acari) in the House Sparrows, Passer Domesticus
Short Communication ISSN 1984-2961 (Electronic) www.cbpv.org.br/rbpv Braz. J. Vet. Parasitol., Jaboticabal, v. 27, n. 4, p. 597-603, oct.-dec. 2018 Doi: https://doi.org/10.1590/S1984-296120180064 Rhinonyssidae (Acari) in the house sparrows, Passer domesticus (Linnaeus, 1758) (Passeriformes: Passeridae), from southern Brazil Ácaros nasais Rhinonyssidae parasitos de Passer domesticus (Linnaeus, 1758) (Passeriformes: Passeridae) no extremo sul do Brasil Luciana Siqueira Silveira dos Santos1*; Carolina Silveira Mascarenhas2; Paulo Roberto Silveira dos Santos3; Nara Amélia da Rosa Farias1 1 Laboratório de Parasitologia, Departamento de Microbiologia e Parasitologia, Instituto de Biologia, Universidade Federal de Pelotas – UFPel, Capão do Leão, RS, Brasil 2 Laboratório de Parasitologia de Animais Silvestres, Departamento de Microbiologia e Parasitologia, Instituto de Biologia, Universidade Federal de Pelotas – UFPel, Capão do Leão, RS, Brasil 3 Centro Nacional de Pesquisa para a Conservação das Aves Silvestres – CEMAVE, Instituto Chico Mendes de Conservação da Biodiversidade – ICMBio, Pelotas, RS, Brasil Received March 29, 2018 Accepted August 7, 2018 Abstract We report the occurrence and infection parameters of two species of nasal mites in Passer domesticus (Linnaeus, 1758) (house sparrow). Nasal passages, trachea, lungs, and air sacs of 100 house sparrows captured in an urban area at the city of Pelotas, State of Rio Grande do Sul, southern Brazil, were examined with a stereomicroscope. The mite, Sternostoma tracheacolum Lawrence, 1948 was present in the trachea and/or lungs (or both) of 13 birds (13%) at a mean intensity of 6.7 mites/infected host. Ptilonyssus hirsti (Castro & Pereira, 1947) was found in the nasal cavity of 1 sparrow (1%); coinfection was not observed in this bird. -
Dieter Thomas Tietze Editor How They Arise, Modify and Vanish
Fascinating Life Sciences Dieter Thomas Tietze Editor Bird Species How They Arise, Modify and Vanish Fascinating Life Sciences This interdisciplinary series brings together the most essential and captivating topics in the life sciences. They range from the plant sciences to zoology, from the microbiome to macrobiome, and from basic biology to biotechnology. The series not only highlights fascinating research; it also discusses major challenges associated with the life sciences and related disciplines and outlines future research directions. Individual volumes provide in-depth information, are richly illustrated with photographs, illustrations, and maps, and feature suggestions for further reading or glossaries where appropriate. Interested researchers in all areas of the life sciences, as well as biology enthusiasts, will find the series’ interdisciplinary focus and highly readable volumes especially appealing. More information about this series at http://www.springer.com/series/15408 Dieter Thomas Tietze Editor Bird Species How They Arise, Modify and Vanish Editor Dieter Thomas Tietze Natural History Museum Basel Basel, Switzerland ISSN 2509-6745 ISSN 2509-6753 (electronic) Fascinating Life Sciences ISBN 978-3-319-91688-0 ISBN 978-3-319-91689-7 (eBook) https://doi.org/10.1007/978-3-319-91689-7 Library of Congress Control Number: 2018948152 © The Editor(s) (if applicable) and The Author(s) 2018. This book is an open access publication. Open Access This book is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made. -
Scientific Note
Journal of the American Mosquito Control Association, 2l(4):474-476,2OO5 Copyright @ 2005 by the American Mosquito Control Association, Inc. SCIENTIFIC NOTE DETECTION OF WEST NILE VIRUS RNA FROM THE LOUSE FLY ICO STA AMERICANA (DIPTERA: HIPPOBOSCIDAE) ARY FARAJOLLAHI,'.' WAYNE J. CRANS,I DIANE NICKERSON,3 PATRICIA BRYANT4 BRUCE WOLE4 AMY GLASER,5 INn THEODORE G. ANDREADIS6 ABSTRACT West Nile virus (WNV) was detected by Taqman reverse transcription-polymerase chain reaction in 4 of 85 (4.7Vo) blood-engorged (n : 2) and unengorged (n : 2) Icosta americana (Leach) hippoboscid flies that were collected from wild raptors submitted to a wildlife rehabilitation center in Mercer County, NJ, in 2003. This report represents an additional detection of WNV in a nonculicine arthropod in North America and the first documented detection of the virus in unengorged hippoboscid flies, further suggesting a possible role that this species may play in the transmission of WNV in North America. KEY WORDS West Nile vrrns, Icosta americana, Hippoboscidae, raptors West Nile virus (WNV) is a flavivirus that rs blood feeders that are commonly associated with principally maintained in an enzootic cycle between birds of prey. Both sexes readily take blood (Be- Culex mosquitoes and avian amplifying hosts. To quaert 1952, 1953; Maa and Peterson 1987) and date, the virus has been detected in or isolated from females are viviparous, exhibiting a high frequency 59 species of mosquitoes in the United States and of blood feeding due to nutritional demands of de- Canada (CDC 2004) and the importance of mos- veloping larvae (Bequaert 1952). Host speciflcity quitoes as enzootic and epidemic vectors of WNV varies greatly among bird-feeding species (Lloyd in North America is well established (Andreadis et 2OO2),bult most species remain and feed on the host al. -
The External Parasites of Birds: a Review
THE EXTERNAL PARASITES OF BIRDS: A REVIEW BY ELIZABETH M. BOYD Birds may harbor a great variety and numher of ectoparasites. Among the insects are biting lice (Mallophaga), fleas (Siphonaptera), and such Diptera as hippohoscid flies (Hippohoscidae) and the very transitory mosquitoes (Culicidae) and black flies (Simuliidae), which are rarely if every caught on animals since they fly off as soon as they have completed their blood-meal. One may also find, in birds ’ nests, bugs of the hemipterous family Cimicidae, and parasitic dipterous larvae that attack nestlings. Arachnida infesting birds comprise the hard ticks (Ixodidae), soft ticks (Argasidae), and certain mites. Most ectoparasites are blood-suckers; only the Ischnocera lice and some species of mites subsist on skin components. The distribution of ectoparasites on the host varies with the parasite concerned. Some show no habitat preference while others tend to confine themselves to, or even are restricted to, definite areas on the body. A list of 198 external parasites for 2.55 species and/or subspecies of birds east of the Mississippi has been compiled by Peters (1936) from files of the Bureau of Entomology and Plant Quarantine between 1928 and 1935. Fleas and dipterous larvae were omitted from this list. According to Peters, it is possible to collect three species of lice, one or two hippoboscids, and several types of mites on a single bird. He records as many as 15 species of ectoparasites each from the Bob-white (Co&us uirginianus), Song Sparrow (Melospiza melodia), and Robin (Turdus migratorius). The lice and plumicolous mites, however, are typically the most abundant forms present on avian hosts.