Host=Flea ~Lationships of Payne County, Oklahoma
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Resource Predictability and Host Specificity in Fleas
81 Resource predictability and host specificity in fleas: the effect of host body mass B. R. KRASNOV1*, S. MORAND2,D.MOUILLOT3,G.I.SHENBROT1, I. S. KHOKHLOVA4 and R. POULIN5 1 Ramon Science Center and Mitrani Department of Desert Ecology, Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, P.O. Box 194, Mizpe Ramon 80600, Israel 2 Center for Biology and Management of Populations, Campus International de Baillarguet, CS 30016 34988 Montferrier-sur-Lez cedex, France 3 UMR CNRS-UMII 5119 Ecosystemes Lagunaires, University of Montpellier II, CC093, FR-34095 Montpellier Cedex 5, France 4 Desert Animals Adaptations and Husbandry, Wyler Department of Dryland Agriculture, Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel 5 Department of Zoology, University of Otago, P.O. Box 56, Dunedin, New Zealand (Received 22 November 2005; revised 28 December 2005; accepted 24 January 2006; first published online 28 March 2006) SUMMARY Ecological specialization is hypothesized to result from the exploitation of predictable resource bases. For parasitic organisms, one prediction is that parasites of large-bodied host species, which tend to be long-lived, should specialize on these hosts, whereas parasites of small host species, which represent more ephemeral and less predictable resources, should become generalists. We tested this prediction by quantifying the association between the level of host specificity of fleas and the mean body mass of their mammalian hosts, using published data from 2 large, distinct geographical regions (South Africa and northern North America). In general, we found supporting evidence that flea host specificity, measured either as the number of host species exploited or their taxonomic distinctness, became more pronounced with increasing host body mass. -
Royal Entomological Society
Royal Entomological Society HANDBOOKS FOR THE IDENTIFICATION OF BRITISH INSECTS To purchase current handbooks and to download out-of-print parts visit: http://www.royensoc.co.uk/publications/index.htm This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 2.0 UK: England & Wales License. Copyright © Royal Entomological Society 2012 ROYAL ENTOMOLOGICAL , SOCIETY OF LONDON Vol. I. Part 1 (). HANDBOOKS FOR THE IDENTIFICATION OF BRITISH INSECTS SIPHONAPTERA 13y F. G. A. M. SMIT LONDON Published by the Society and Sold at its Rooms - 41, Queen's Gate, S.W. 7 21st June, I9S7 Price £1 os. od. ACCESSION NUMBER ....... ................... British Entomological & Natural History Society c/o Dinton Pastures Country Park, Davis Street, Hurst, OTS - Reading, Berkshire RG 10 OTH .•' Presented by Date Librarian R EGULATIONS I.- No member shall be allowed to borrow more than five volumes at a time, or to keep any of tbem longer than three months. 2.-A member shall at any time on demand by the Librarian forthwith return any volumes in his possession. 3.-Members damaging, losing, or destroying any book belonging to the Society shall either provide a new copy or pay such sum as tbe Council shall tbink fit. ) "1' > ) I .. ··•• · ·• "V>--· .•. .t ... -;; ·· · ·- ~~- -~· · · ····· · · { · · · l!i JYt.11'ian, ,( i-es; and - REGU--LATIONS dthougll 1.- Books may b - ~dapted, ; ~ 2 -~ . e borrowed at . !.l :: - --- " . ~ o Member shall b . all Meeflfll(s of the So J t Volumes at a time o; ,IJJowed to borrow more c e y . 3.- An y Mem ber r t '. to keep them lonl{er th than three b.ecorn_e SPecified f e a Jn!ng a \'oJume a n one m on th. -
United States Department of the Interior
United States Department of the Interior FISH AND WILDLIFE SERVICE South Florida Ecological Services Office 1339 20” Street Vero Beach, Florida 32960 March 25, 2015 Kevin R. Becker Department of the Air Force Detachment 1, 23rd Wing Avon Park Air/Ground Training Complex (ACC) Avon Park Air Force Range, Florida 33825 Service CPA Code: 2013-CPA-0255 Service Consultation Code: 2013-F-0271 Date Received: September 3, 2013 Project: Avon Park AFR, JIFE Counties: Highlands and Polk Dear Lieutenant Colonel Beeker: This document transmits the U. S. Fish and Wildlife Service’s (Service) biological opinion based on our review of the U.S. Air Force’s (USAF) proposed Joint Integrated Fires Exercises (JIFE) at Avon Park Air Force Range (APAFR) in Highlands and Polk Counties, Florida, and its adverse effects on the threatened eastern indigo snake (Drymarchon corals couperi) (indigo snake), threatened Florida scrub-jay (Aphelocoma coerulescens) (scrub-jay), endangered red-cockaded woodpecker (Picoides borealis) (RCW), and endangered Florida bonneted bat (Eumops floridanus) (FBB) in accordance with section 7 of the Endangered Species Act of 1973, as amended (Act) (87 Stat. 884; 16 U.S.C. 1531 etseq.). This Biological Opinion is based on information provided in the USAF’s August 28, 2013, biological assessment (BA), conversations, and other sources of information. A complete administrative record of this consultation is on file in the South Florida Ecological Services Office, Vero Beach, Florida. Consultation History On May 2, 2013, the USAF requested the assistance of the Service with the review of their draft BA for the JIFE. On May 8, 2013, the Service sent the USAF an email with comments on the draft BA. -
Fleas, Hosts and Habitat: What Can We Predict About the Spread of Vector-Borne Zoonotic Diseases?
2010 Fleas, Hosts and Habitat: What can we predict about the spread of vector-borne zoonotic diseases? Ph.D. Dissertation Megan M. Friggens School of Forestry I I I \, l " FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? by Megan M. Friggens A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Forest Science Northern Arizona University May 2010 ?Jii@~-~-u-_- Robert R. Parmenter, Ph. D. ~",l(*~ l.~ Paulette L. Ford, Ph. D. --=z:r-J'l1jU~ David M. Wagner, Ph. D. ABSTRACT FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? MEGAN M. FRIGGENS Vector-borne diseases of humans and wildlife are experiencing resurgence across the globe. I examine the dynamics of flea borne diseases through a comparative analysis of flea literature and analyses of field data collected from three sites in New Mexico: The Sevilleta National Wildlife Refuge, the Sandia Mountains and the Valles Caldera National Preserve (VCNP). My objectives were to use these analyses to better predict and manage for the spread of diseases such as plague (Yersinia pestis). To assess the impact of anthropogenic disturbance on flea communities, I compiled and analyzed data from 63 published empirical studies. Anthropogenic disturbance is associated with conditions conducive to increased transmission of flea-borne diseases. Most measures of flea infestation increased with increasing disturbance or peaked at intermediate levels of disturbance. Future trends of habitat and climate change will probably favor the spread of flea-borne disease. -
Hastings Slide Collection3
HASTINGS NATURAL HISTORY RESERVATION SLIDE COLLECTION 1 ORDER FAMILY GENUS SPECIES SUBSPECIES AUTHOR DATE # SLIDES COMMENTS/CORRECTIONS Siphonaptera Ceratophyllidae Diamanus montanus Baker 1895 221 currently Oropsylla (Diamanus) montana Siphonaptera Ceratophyllidae Diamanus spp. 1 currently Oropsylla (Diamanus) spp. Siphonaptera Ceratophyllidae Foxella ignota acuta Stewart 1940 402 syn. of F. ignota franciscana (Roths.) Siphonaptera Ceratophyllidae Foxella ignota (Baker) 1895 2 Siphonaptera Ceratophyllidae Foxella spp. 15 Siphonaptera Ceratophyllidae Malaraeus spp. 1 Siphonaptera Ceratophyllidae Malaraeus telchinum Rothschild 1905 491 M. telchinus Siphonaptera Ceratophyllidae Monopsyllus fornacis Jordan 1937 57 currently Eumolpianus fornacis Siphonaptera Ceratophyllidae Monopsyllus wagneri (Baker) 1904 131 currently Aetheca wagneri Siphonaptera Ceratophyllidae Monopsyllus wagneri ophidius Jordan 1929 2 syn. of Aetheca wagneri Siphonaptera Ceratophyllidae Opisodasys nesiotus Augustson 1941 2 Siphonaptera Ceratophyllidae Orchopeas sexdentatus (Baker) 1904 134 Siphonaptera Ceratophyllidae Orchopeas sexdentatus nevadensis (Jordan) 1929 15 syn. of Orchopeas agilis (Baker) Siphonaptera Ceratophyllidae Orchopeas spp. 8 Siphonaptera Ceratophyllidae Orchopeas latens (Jordan) 1925 2 Siphonaptera Ceratophyllidae Orchopeas leucopus (Baker) 1904 2 Siphonaptera Ctenophthalmidae Anomiopsyllus falsicalifornicus C. Fox 1919 3 Siphonaptera Ctenophthalmidae Anomiopsyllus congruens Stewart 1940 96 incl. 38 Paratypes; syn. of A. falsicalifornicus Siphonaptera -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
The Fleas (Siphonaptera) in Iran: Diversity, Host Range, and Medical Importance
RESEARCH ARTICLE The Fleas (Siphonaptera) in Iran: Diversity, Host Range, and Medical Importance Naseh Maleki-Ravasan1, Samaneh Solhjouy-Fard2,3, Jean-Claude Beaucournu4, Anne Laudisoit5,6,7, Ehsan Mostafavi2,3* 1 Malaria and Vector Research Group, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran, 2 Research Centre for Emerging and Reemerging infectious diseases, Pasteur Institute of Iran, Akanlu, Kabudar Ahang, Hamadan, Iran, 3 Department of Epidemiology and Biostatistics, Pasteur institute of Iran, Tehran, Iran, 4 University of Rennes, France Faculty of Medicine, and Western Insitute of Parasitology, Rennes, France, 5 Evolutionary Biology group, University of Antwerp, Antwerp, Belgium, 6 School of Biological Sciences, University of Liverpool, Liverpool, United Kingdom, 7 CIFOR, Jalan Cifor, Situ Gede, Sindang Barang, Bogor Bar., Jawa Barat, Indonesia * [email protected] a1111111111 a1111111111 a1111111111 a1111111111 Abstract a1111111111 Background Flea-borne diseases have a wide distribution in the world. Studies on the identity, abun- dance, distribution and seasonality of the potential vectors of pathogenic agents (e.g. Yersi- OPEN ACCESS nia pestis, Francisella tularensis, and Rickettsia felis) are necessary tools for controlling Citation: Maleki-Ravasan N, Solhjouy-Fard S, and preventing such diseases outbreaks. The improvements of diagnostic tools are partly Beaucournu J-C, Laudisoit A, Mostafavi E (2017) The Fleas (Siphonaptera) in Iran: Diversity, Host responsible for an easier detection of otherwise unnoticed agents in the ectoparasitic fauna Range, and Medical Importance. PLoS Negl Trop and as such a good taxonomical knowledge of the potential vectors is crucial. The aims of Dis 11(1): e0005260. doi:10.1371/journal. this study were to make an exhaustive inventory of the literature on the fleas (Siphonaptera) pntd.0005260 and range of associated hosts in Iran, present their known distribution, and discuss their Editor: Pamela L. -
NCUE 2008 Text Pgs 1-144 11.4.08.Indd
CORPORATE SPONSORS To be a corporate sponsor of the National Conference on Urban Entomology is to be a benefactor of programs supported by the conference, a supporter of current entomological activities in the areas of urban entomology, and a partner in promoting a better understanding of the science of urban entomology. The following are the National Conference on Urban Entomology corporate sponsors for 2008 (in alphabetical order): BASF Corporation Bayer Environmental Science Dow AgroSciences DuPont Professional Products MGK-McLaughlin Gormley King Company Orkin, Inc. Pest Control Technology Magazine Pest Management Professional Magazine S. C. Johnson & Son, Inc. Syngenta Crop Protection, Inc. Terminix International Whitmire Micro-Gen THANK YOU FOR YOUR SUPPORT! Proceedings cover was adapted from Tim Cabrera’s design for the 2008 National Conference on Urban Entomology Program cover, which refl ected the theme “Urban Pest Roundup.” PROCEEDINGS OF THE 2008 NATIONAL CONFERENCE ON URBAN ENTOMOLOGY Edited by Susan C. Jones ACKNOWLEDGMENTS David J. Shetlar (Ohio State University) generously provided expertise with graphics and print formatting; his assistance was invaluable. I would like to thank Megan E. Meuti, Lauren N. Tryon, and El-Desouky Ammar (Ohio State University) for help inputting and formatting text and proofreading the manuscript. Karen M. Vail (University of Tennessee), Dini M. Miller (Virginia Tech), and Laura Nelson (Texas A&M University) also are thanked for their assistance with various aspects of the Proceedings. Tim Cabrera is gratefully acknowledged for designing the 2008 National Conference on Urban Entomology Program cover. TABLE OF CONTENTS National Conference On Urban Entomology May 18-21, 2008 Tulsa, Oklahoma U.S.A. -
Biodiversity from Caves and Other Subterranean Habitats of Georgia, USA
Kirk S. Zigler, Matthew L. Niemiller, Charles D.R. Stephen, Breanne N. Ayala, Marc A. Milne, Nicholas S. Gladstone, Annette S. Engel, John B. Jensen, Carlos D. Camp, James C. Ozier, and Alan Cressler. Biodiversity from caves and other subterranean habitats of Georgia, USA. Journal of Cave and Karst Studies, v. 82, no. 2, p. 125-167. DOI:10.4311/2019LSC0125 BIODIVERSITY FROM CAVES AND OTHER SUBTERRANEAN HABITATS OF GEORGIA, USA Kirk S. Zigler1C, Matthew L. Niemiller2, Charles D.R. Stephen3, Breanne N. Ayala1, Marc A. Milne4, Nicholas S. Gladstone5, Annette S. Engel6, John B. Jensen7, Carlos D. Camp8, James C. Ozier9, and Alan Cressler10 Abstract We provide an annotated checklist of species recorded from caves and other subterranean habitats in the state of Georgia, USA. We report 281 species (228 invertebrates and 53 vertebrates), including 51 troglobionts (cave-obligate species), from more than 150 sites (caves, springs, and wells). Endemism is high; of the troglobionts, 17 (33 % of those known from the state) are endemic to Georgia and seven (14 %) are known from a single cave. We identified three biogeographic clusters of troglobionts. Two clusters are located in the northwestern part of the state, west of Lookout Mountain in Lookout Valley and east of Lookout Mountain in the Valley and Ridge. In addition, there is a group of tro- globionts found only in the southwestern corner of the state and associated with the Upper Floridan Aquifer. At least two dozen potentially undescribed species have been collected from caves; clarifying the taxonomic status of these organisms would improve our understanding of cave biodiversity in the state. -
Iowa State College Journal of Science 18.2
IOWA STATE COLLEGE JOURNAL OF SCIENCE Published on the first day of October, January, April, and July EDITORIAL BOARD EDITOR-JN-CHIEF. Joseph C. Gilman. AssrsTANT EnrToR, H. E. Ingle. CONSULTING EDITORS: R. E. Buchanan, C. J. Drake, I. E. Melhus, E. A. Benbrook, P. Mabel Nelson, V. E. Nelson, C. H. Brown, Jay W. Woodrow. From Sigma Xi: E. W. Lindstrom, D. L. Holl, C. H. Werkman. All manuscripts submitted ~~Quld be apdressed to J . C. Gilman, Botany Hall, Iowa St_a.t~ !Go~e~e.: !f..~s. I!J"!a; • : • • , . ~ . .. All remittances sfulolB :be ~tldr~~sed° to ~~.,"dQ~iiate Press, Inc., Col legiate Press Buildir\g, f\,m,.e9. lewa. • • • I • •• • • • • 0 Single CoP.~~s;''1.0ll ci;_c~~ V~.t~ ~~Il,:il0''. ~$2.QO}.•.A:U,.ual Subscrip tion: ~3 . ao;:in'Ca!'lada.$3.25~ Forei~. $S.!i0. ~ •• •• : ••• : ·· ~ .·· .............. :· ·: . .: .. : .....·. ·. ... ··= .. : ·.······ Entered as second-class matter January 16, 1935, at the postoffice at Ames, Iowa, under the act of March 3, 1879. THE COCCIDIA OF WILD RABBITS OF IOWA II. EXPERIMENTAL STUDIES WITH EIMERIA NEOLEPORIS CARVALHO, 1942' Jos:E C. M. CARVALHO' From the Entomology and Economic Zoology Section, Iowa Agricultural Experiment Station and the Fish and Wildlife Service, United States Department of the Interior Received December 10, 1942 During the author's experiments with coccidia of wild rabbits in Iowa, the most complete studies were made with E. neoleporis, because it was able to grow in the tame rabbit. Experiments were carried on to observe its behavior, life cycle, biometrical or physiological changes, immunity relationships, etc., in the latter host. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Morphology Reveals the Unexpected Cryptic Diversity in Ceratophyllus Gallinae (Schrank, 1803) Infested Cyanistes Caeruleus Linnaeus, 1758 Nest Boxes
Acta Parasitologica (2020) 65:874–881 https://doi.org/10.1007/s11686-020-00239-6 ORIGINAL PAPER Morphology Reveals the Unexpected Cryptic Diversity in Ceratophyllus gallinae (Schrank, 1803) Infested Cyanistes caeruleus Linnaeus, 1758 Nest Boxes Olga Pawełczyk1 · Tomasz Postawa2 · Marian Blaski3 · Krzysztof Solarz1 Received: 6 June 2019 / Accepted: 29 May 2020 / Published online: 8 June 2020 © The Author(s) 2020 Abstract Purpose The main aim of our study was to examine morphological diferentiation between and within sex of hen feas— Ceratophyllus gallinae (Schrank, 1803) population collected from Eurasian blue tit (Cyanistes caeruleus Linnaeus, 1758), inhabiting nest boxes and to determine the morphological parameters diferentiating this population. Methods A total of 296 feas were collected (148 females and 148 males), determined to species and sex, then the following characters were measured in each of the examined feas: body length, body width, length of head, width of head, length of comb, height of comb, length of tarsus, length of thorax and length of abdomen. Results The comparison of body size showed the presence of two groups among female and male life forms of the hen fea, which mostly difered in length of abdomen, whereas the length of head and tarsus III were less variable. Conclusion Till now, the only certain information is the presence of two adult life forms of C. gallinae. The genesis of their creation is still unknown and we are not able to identify the mechanism responsible for the morphological diferentiation of feas collected from the same host. In order to fnd answer to this question, future research in the feld of molecular taxonomy is required.