First Collection Records of Phlebotomine Sand Flies (Diptera: Psychodidae) from New Jersey

Total Page:16

File Type:pdf, Size:1020Kb

First Collection Records of Phlebotomine Sand Flies (Diptera: Psychodidae) from New Jersey SHORT COMMUNICATION First Collection Records of Phlebotomine Sand Flies (Diptera: Psychodidae) From New Jersey 1,2 3 1 DANA C. PRICE, DONALD E. GUNTHER, AND RANDY GAUGLER J. Med. Entomol. 48(2): 476Ð478 (2011); DOI: 10.1603/ME10170 ABSTRACT The phlebotomine sand ßies Lutzomyia (Psathyromyia) shannoni (Dyar) and Lut- zomyia (Helcocyrtomyia) vexator (Coquillett) are reported for the Þrst time from New Jersey. Both species were collected from ultraviolet CO2-baited Centers for Disease Control light traps during a state-wide phlebotomine survey conducted in 2007 and 2008. L. shannoni has previously been reported from New Jersey; however, this observation was made in error. These collections do not represent a northern range expansion for either species. KEY WORDS phlebotomine, sand ßy, leishmaniasis, Lutzomyia shannoni, Lutzomyia vexator The phlebotomine sand ßy genus Lutzomyia contains shannoni exhibit facultative autogeny in the labora- Ϸ400 species (Young and Duncan 1994), of which 14 tory, although they will readily take multiple blood- are found in North America (Young and Perkins meals to facilitate egg development (Young and Per- 1984). We report, for the Þrst time, collections of kins 1984, Young and Duncan 1994). Oviposition and Lutzomyia (Psathyromyia) shannoni (Dyar) and Lut- larval development occur in cryptic habitats (crevices, zomyia (Helcocyrtomyia) vexator (Coquillett) from burrows, tree holes) rich in organic detritus (Rosabal New Jersey. These are the Þrst collections of any and Miller 1970). This species feeds on large warm- phlebotomine from within the state, and the only two blooded hosts, including deer, swine, and humans species known to occur in the northeastern United (Comer et al. 1994). States. Previous reports of L. shannoni from southern L. vexator has a broad distribution, ranging from New Jersey (Ostfeld et al. 2004, Duprey et al. 2006) Mexico to the Canadian provinces of Alberta and were erroneously based on misinterpretation of a map Ontario, and spans both coasts of the United States. It marker located over Wilmington, Delaware, as being has been recorded from Alabama, Arkansas, Califor- within New Jersey (Young and Perkins 1984) (R. nia, Colorado, Connecticut, Florida, Georgia, Ken- Ostfeld, personal communication). tucky, Louisiana, Maryland, Montana, Mississippi, L. shannoni is associated with hardwood forest hab- New Mexico, New York, Ohio, Oklahoma, Tennessee, itats ranging from Argentina to the northeastern Texas, Virginia, Washington, and Wyoming (Young United States (Young and Perkins 1984). Adult ßies and Perkins 1984, Ostfeld et al. 2004, Haddow et al. are generally collected from, or in proximity to, but- 2008, Minter et al. 2009). The species has been re- tress roots and other tree hole habitats (Comer et al. corded from diverse habitats ranging from grassland 1993). Phlebotomines are weak ßiers, and neither sex and pasture to mixed hardwood forests (Chaniotis and of L. shannoni dispersed Ͼ163 m in previous mark- Anderson 1968, Ostfeld et al. 2004). Gravid females recapture studies (Alexander 1987). Within the oviposit within fecal chambers of rodent burrows, United States, the species has been collected from where the larvae feed on feces before pupation and Arkansas, Alabama, Delaware, Florida, Georgia, Ken- emergence. The host preferences of wild L. vexator tucky, Louisiana, Maryland, Mississippi, North Caro- populations are poorly characterized; however, they lina, Ohio, South Carolina, and Tennessee (Young and have been reported to feed on various reptiles and Perkins 1984, McHugh 2005, Haddow et al. 2008, amphibians (Chaniotis and Anderson 1964). Minter et al. 2009). L. shannoni populations on Os- sabaw Island, Georgia, produced as many as three Materials and Methods generations from April through November and over- wintered as larvae (Comer et al. 1993). Female L. An extensive phlebotomine sand ßy survey was per- formed in New Jersey during 2007 and 2008. Fifty-four 1 Center for Vector Biology, Rutgers University, 180 Jones Avenue, collection sites spanning all 21 counties and Þve phys- New Brunswick, NJ 08901-8536. iographic provinces were sampled for Lutzomyia spp. 2 Corresponding author: Center for Vector Biology, Department of using incandescent and ultraviolet (UV) Centers for Entomology, Rutgers University, 180 Jones Avenue, New Brunswick, Disease Control (CDC) light traps (BioQuip, Rancho NJ 08901Ð8536 (e-mail: [email protected]). 3 Sussex County OfÞce of Mosquito Control, 150 Morris Turnpike, Dominguez, CA) hung from tree branches at a height Newton, NJ 07860. of 0.75 m from trap hood to ground. Traps were sup- 0022-2585/11/0476Ð0478$04.00/0 ᭧ 2011 Entomological Society of America March 2011 PRICE ET AL.: PHLEBOTOMINE SAND FLY COLLECTIONS FROM NEW JERSEY 477 plemented with a canister of compressed CO2 gas (Travi et al. 2002, Lawyer et al. 1987, Claborn et al. Þtted with a 15 psi regulator. A CO2 volume of 500 2009, Ferro et al. 1998). All four pathogens are infec- ml/min was maintained by a ßow rate oriÞce (Clarke tive to humans and are causative agents of visceral (Le. Mosquito Control, Roselle, IL) attached to rubber chagasi), cutaneous (Le. mexicana, Le. major), and tubing. The tube end was hung adjacent to the trap mucocutaneous (Le. panamensis) leishmaniasis. The hood. Each site had two traps, one incandescent and ßy has only been implicated in transmission of Le. one UV, running concurrently for a single trap night. mexicana to date (Lawyer and Young 1987). Comer at Sites were sampled from the period 1 June through 30 al. (1990) found L. shannoni to be an overwintering September, coinciding with the New Jersey State Vec- reservoir and competent vector of vesicular stomatitis tor Surveillance Program. In addition, individual New virus New Jersey serotype in Georgia. Collections of Jersey county mosquito control programs from 10 this species from Delaware have been made farther counties provided bycatch from New Jersey Light north along the Atlantic coast; thus, this collection Traps (John W. Hock, Gainesville, FL) used to track does not represent a northerly expansion of its range. adult mosquito populations. Adult male Lutzomyia L. vexator exhibits vector-borne disease potential spp. were identiÞed using the keys of Young and Per- among cold-blooded vertebrates. Anderson and Ayala kins (1984) and placed in the Rutgers University En- (1968) found that California toads (Bufo boreas halo- tomological Museum. philus) became infected with an unknown trypano- some after feeding on infected L. vexator. Hemogre- garines of the genus Hepatozoon, thought to be derived Results and Discussion from wild snakes, have been isolated from this sand ßy The Þrst and only record of L. shannoni from New (Ayala 1973). It is the primary vector of Plasmodium Jersey is represented by a single male collected from mexicanum, or saurian malaria, in the western fence an UV CDC light trap on 27 August 2007. The site was lizard (Sceloporus occidentalis) (Ayala 1971). The located in Salem County, Pennsville (39Њ38ЈN, eastern fence lizard (Sceloporus undulates) is highly Ϫ75Њ29ЈW), and consisted of a deciduous hardwood susceptible to P. mexicanum, as 69% showed infection forest located in the extreme southwest of the inner after a single L. vexator bite (Klein et al. 1987). coastal plain province at an elevation of approximately The presence of these hematophagous insects 2 m. Tree type was predominantly oak (Quercus spp.) within New Jersey, coupled with their vector poten- interspersed with low-lying holly (Ilex spp.). Subse- tial, warrants further study as to their exact range, host quent collections from this site and the surrounding preference, and vectorial capacity. Ostfeld et al. area in August 2007 and July 2008 yielded no other (2004), in responding to a Leishmania infantum out- specimens. break in a New York foxhound kennel, light-trapped We collected the Þrst records of L. vexator (six the immediate area for potential phlebotomine vec- males and nine females) in New Jersey from incan- tors. They recorded the Þrst specimens of L. vexator in descent and UV CDC light traps on 29 July 2008. The the state Ͻ10 km away from the disease focus. A site was located in Sussex County, Sussex (41Њ15Ј N, follow-up study conducted between April 2000 and Ϫ74Њ30Ј W), at an elevation of 290 m within the high- December 2003 noted at least one hunting club in New lands region of the Appalachian Mountains. Tree type Jersey with hounds positive for Leishmania spp. (Du- consisted primarily of red maple (Acer rubrum) and prey et al. 2006). Although the authors hypothesized oak (Quercus spp.). Rocky outcroppings of crystalline dog-to-dog mechanical transmission as the cause for metamorphic rock were plentiful, as were rodent bur- the Leishmania outbreak, the discovery of L. shannoni rows, exposed tree roots, and extreme slope, all of within New Jersey coupled with previous isolations of which have previously been associated with L. vexator this pathogen should extend vector research within (Ostfeld et al. 2004). A subsequent collection made the state beyond the borders of mosquitoes. from the same site during the trap night of 10 August 2009 yielded large numbers of phlebotomines. A single UV light trap placed 1 m from the base of a steep rock Acknowledgments shelf collected 104 L. vexator. An identical trap placed 12 m away collected 20 sand ßies. Additionally, eight We thank D. Carle, N. Slavin, and M. Groncki for assis- tance with Þeld collections, and Ary Farajollahi for edits to locations within a 1,200-m radius of the initial collec- this manuscript. We thank all 21 New Jersey county mosquito tion site were sampled for L. vexator, with all collecting control programs for providing trap bycatch and/or logistical sand ßies. Expanded surveillance yielded collections support. This is New Jersey Agricultural Experiment Station of one to four sand ßies from three additional locations Publication D-08-08292-02-10 (supported by state funds with as far away as 25 km, indicating this species is distrib- partial support from the New Jersey State Mosquito Control uted throughout extreme northwestern New Jersey, Commission and the New Jersey Mosquito Control Associ- but is only locally abundant.
Recommended publications
  • Genetic Variability Among Populations of Lutzomyia
    Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 96(2): 189-196, February 2001 189 Genetic Variability among Populations of Lutzomyia (Psathyromyia) shannoni (Dyar 1929) (Diptera: Psychodidae: Phlebotominae) in Colombia Estrella Cárdenas/+, Leonard E Munstermann*, Orlando Martínez**, Darío Corredor**, Cristina Ferro Laboratorio de Entomología, Instituto Nacional de Salud, Avenida Eldorado, Carrera 50, Zona Postal 6, Apartado Aéreo 80080, Bogotá DC, Colombia *Department of Epidemiology and Public Health, School of Medicine, Yale University, New Haven, CT, USA **Facultad de Agronomía, Universidad Nacional de Colombia, Bogotá DC, Colombia Polyacrylamide gel electrophoresis was used to elucidate genetic variation at 13 isozyme loci among forest populations of Lutzomyia shannoni from three widely separated locations in Colombia: Palambí (Nariño Department), Cimitarra (Santander Department) and Chinácota (Norte de Santander Depart- ment). These samples were compared with a laboratory colony originating from the Magdalena Valley in Central Colombia. The mean heterozygosity ranged from 16 to 22%, with 2.1 to 2.6 alleles detected per locus. Nei’s genetic distances among populations were low, ranging from 0.011 to 0.049. The esti- mated number of migrants (Nm=3.8) based on Wright’s F-Statistic, FST, indicated low levels of gene flow among Lu. shannoni forest populations. This low level of migration indicates that the spread of stomatitis virus occurs via infected host, not by infected insect. In the colony sample of 79 individuals, 0.62 0.62 the Gpi locus was homozygotic ( /0.62) in all females and heterozygotic ( /0.72) in all males. Al- though this phenomenon is probably a consequence of colonization, it indicates that Gpi is linked to a sex determining locus.
    [Show full text]
  • Life Tables and Reproductive Parameters of Lutzomyia Spinicrassa (Diptera: Psychodidae) Under Laboratory Conditions
    Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 99(6): 603-607, October 2004 603 Life Tables and Reproductive Parameters of Lutzomyia spinicrassa (Diptera: Psychodidae) under Laboratory Conditions Jesús Escovar, Felio J Bello/+, Alberto Morales, Ligia Moncada*, Estrella Cárdenas Laboratorio de Entomología, Biología Celular y Genética, Departamento de Ciencias Básicas, Universidad de La Salle, Bogotá DC, Colombia *Laboratorio de Parasitología, Facultad de Medicina, Universidad Nacional de Colombia, Bogotá DC, Colombia Lutzomyia spinicrassa is a vector of Leishmania braziliensis in Colombia. This sand fly has a broad geographical distribution in Colombia and Venezuela and it is found mainly in coffee plantations. Baseline biological growth data of L. spinicrassa were obtained under experimental laboratory conditions. The development time from egg to adult ranged from 59 to 121 days, with 12.74 weeks in average. Based on cohorts of 100 females, horizontal life table was constructed. The following predictive parameters were obtained: net rate of reproduction (8.4 females per cohort female), generation time (12.74 weeks), intrinsic rate of population increase (0.17), and finite rate of population increment (1.18). The reproductive value for each class age of the cohort females was calculated. Vertical life tables were elaborated and mortality was described for the generation obtained of the field cohort. In addition, for two successive generations, additive variance and heritability for fecundity were estimated. Key words: Lutzomyia spinicrassa - life cycle - reproduction - population - heritability The sand fly Lutzomyia spinicrassa (Morales, Osor- shannoni, Cabrera et al. (1999) with L. ovallesi and Cabrera no-Mesa, Osorno & de Hoyos, 1969) belongs to the group and Ferro (2000) with three species of Lutzomyia of the verrucarum, series townsendi and it has a wide geographi- group verrucarum.
    [Show full text]
  • Detection of Vesicular Stomatitis Virus Indiana from Insects Collected During the 2020 Outbreak in Kansas, USA
    pathogens Article Detection of Vesicular Stomatitis Virus Indiana from Insects Collected during the 2020 Outbreak in Kansas, USA Bethany L. McGregor 1,† , Paula Rozo-Lopez 2,† , Travis M. Davis 1 and Barbara S. Drolet 1,* 1 Arthropod-Borne Animal Diseases Research Unit, Center for Grain and Animal Health Research, Agricultural Research Service, United States Department of Agriculture, Manhattan, KS 66502, USA; [email protected] (B.L.M.); [email protected] (T.M.D.) 2 Department of Entomology, Kansas State University, Manhattan, KS 66506, USA; [email protected] * Correspondence: [email protected] † These authors contributed equally to this work. Abstract: Vesicular stomatitis (VS) is a reportable viral disease which affects horses, cattle, and pigs in the Americas. Outbreaks of vesicular stomatitis virus New Jersey serotype (VSV-NJ) in the United States typically occur on a 5–10-year cycle, usually affecting western and southwestern states. In 2019–2020, an outbreak of VSV Indiana serotype (VSV-IN) extended eastward into the states of Kansas and Missouri for the first time in several decades, leading to 101 confirmed premises in Kansas and 37 confirmed premises in Missouri. In order to investigate which vector species contributed to the outbreak in Kansas, we conducted insect surveillance at two farms that experienced confirmed VSV-positive cases, one each in Riley County and Franklin County. Centers for Disease Control and Prevention miniature light traps were used to collect biting flies on the premises. Two genera of known VSV vectors, Culicoides biting midges and Simulium black flies, were identified to species, Citation: McGregor, B.L.; Rozo- pooled by species, sex, reproductive status, and collection site, and tested for the presence of VSV- Lopez, P.; Davis, T.M.; Drolet, B.S.
    [Show full text]
  • 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.
    [Show full text]
  • Section IV: Preventive Medicine and Public Health Services
    Veterinary Support in the Irregular Warfare Environment Section IV: Preventive Medicine and Public Health Services A US Army veterinarian from the 490th Civil Affairs Battalion Functional Specialty Team and a community animal health worker (second from left) work together to treat a young camel during an 8-day Veterinary Civic Action Program in Negele, Ethiopia, August 23, 2011. Using deployed US veterinary personnel helps develop the host nation’s surveillance programs and laboratory capacity, which is not only critical to global zoonotic disease control and surveillance and preventive medicine programs, but also supports the concepts of One Health and nation-building. Photograph: by US Air Force Captain Jennifer Pearson. Reproduced from: https://www.army.mil/article/65682/helping_an_ ethiopian_community_survive_severe_drought. Accessed April 26, 2018. 273 Military Veterinary Services 274 Zoonotic and Animal Diseases of Military Importance Chapter 11 ZOONOTIC AND ANIMAL DISEASES OF MILITARY IMPORTANCE RONALD L. BURKE, DVM, DRPH; TAYLOR B. CHANCE, DVM; KARYN A. HAVAS, DVM, PHD; SAMUEL YINGST, DVM, PhD; PAUL R. FACEMIRE, DVM; SHELLEY P. HONNOLD, DVM, PhD; ERIN M. LONG, DVM; BRETT J. TAYLOR, DVM, MPH; REBECCA I. EVANS, DVM, MPH; ROBIN L. BURKE, DVM, MPH; CONNIE W. SCHMITT, DVM; STEPHANIE E. FONSECA, DVM; REBECCA L. BAXTER, DVM; MICHAEL E. MCCOWN, DVM, MPH; A. RICK ALLEMAN, DVM, PhD; KATHERINE A. SAYLER; LARA S. COTTE, DVM; CLAIRE A. CORNELIUS, DVM, PhD; AUDREY C. MCMILLAN-COLE, DVM, MPVM; KARIN HAMILTON, DVM, MPH; AND KELLY G. VEST, DVM,
    [Show full text]
  • A Sand Fly, Lutzomyia Shannoni Dyar (Insecta: Diptera: Psychodidae: Phlebotomine) 1
    Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY 421 A Sand Fly, Lutzomyia shannoni Dyar (Insecta: Diptera: Psychodidae: Phlebotomine) 1 Rajinder S. Mann, Philip E. Kaufman, and Jerry F. Butler2 Introduction Lutzomyia shannoni Dyar is a proven vector of vesicular stomatitis virus and a suspected vector of Phlebotomine sand flies are of considerable visceral leishmaniasis and sand fly fever in Florida. It public health importance because of their ability to is one of the more thoroughly studied species of transmit several viral, bacterial, and protozoal phlebotomine sand flies in North America. disease-causing organisms of humans and other animals. Distribution Confusion with other types of biting flies is often Sand flies occur in a wide range of habitats and caused because the common name "sand fly" is also individual species often have very specific habitat used for other biting flies of genera Ceratopogon and requirements. Lutzomyia shannoni is distributed from Culicoides. There are about 700 species of Argentina to the United States, including Brazil, phlebotomine sand flies of which about 70 are Columbia, Panama and Costa Rica. Its distribution is considered to transmit disease organisms to people highly disjunct within the range, depending on locally (Adler and Theodor 1957). occurring environmental factors such as frequency of precipitation, temperature, physical barriers, habitat Sand flies are characterized by their densely availability, and the distribution and abundance of hairy wings, giving them a moth-like appearance. vertebrate hosts (Young and Arias 1992). Phlebotomines are distinguished from other members of the family by the way they hold their wings erected In the United States, it has been found through above the body in a vertical "V", whereas members of the southern states from Florida to Louisiana plus other psychodid subfamilies hold their wings flat and Arkansas, Tennessee, South and North Carolina.
    [Show full text]
  • The Epidemiology of La Crosse Virus in Tennessee and West Virginia
    University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 5-2009 The epidemiology of La Crosse virus in Tennessee and West Virginia Andrew Douglas Haddow University of Tennessee Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Recommended Citation Haddow, Andrew Douglas, "The epidemiology of La Crosse virus in Tennessee and West Virginia. " PhD diss., University of Tennessee, 2009. https://trace.tennessee.edu/utk_graddiss/6044 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Andrew Douglas Haddow entitled "The epidemiology of La Crosse virus in Tennessee and West Virginia." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Plants, Soils, and Insects. Reid R. Gerhardt, Major Professor We have read this dissertation and recommend its acceptance: Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) To the Graduate Council: I am submitting herewith a dissertation written by Andrew Douglas Haddow entitled “The Epidemiology of La Crosse Virus in the Tennessee and West Virginia.” I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the requirements for the degree of Doctor of Philosophy, with a major in Plants, Soils, and Insects.
    [Show full text]
  • Suspected Or Known Species on Patuxent Research Refuge
    Appendix A. USFWS USFWS Tree Swallow Suspected or Known Species on Patuxent Research Refuge Appendix A. Suspected or Known Species on Patuxent Research Refuge Table A-1. Suspected or Known Bird Species on Patuxent Research Refuge 1 2 Rank Rank 3 6 5 4 Heritage Heritage Status Refuge E Refuge Status & E on on T & Natural 7 Natural T 30 Common Name Scientific Name Breeding Seasons State BCR Global State Federal WATERBIRDS American Bittern Botaurus lentiginosus G4 S1 S2B I Yr M S1N Anhinga Anhinga anhinga Sp Belted Kingfisher Megaceryle alcyon Yr B Black‐crowned Night Heron Nycticorax nycticorax G5 S3B S2N SpSF M Cattle Egret Bubulcus ibis SpF Common Loon Gavia immer G5 S4N SpF Double‐crested Cormorant Phalacrocorax auritus Yr Glossy Ibis Plegadis falcinellus G5 S4B SpSF H Great Blue Heron Ardea herodias G5 S4B S3 Yr B S4N Great Egret Ardea alba G5 S4B SpSF Green Heron Butorides virescens Yr B Horned Grebe Podiceps auritus G5 S4N SpF H Least Bittern Ixobrychus exilis G5 S2 S3B I SpS B M Little Blue Heron Egretta caerulea G5 S3B SpSF M Pied‐billed Grebe Podilymbus podiceps G5 S2B S3N Yr B Red‐necked Grebe Podiceps grisegena Sp Snowy Egret Egretta thula G5 S3 S4B SpSF M White Ibis Eudocimus albus SF Yellow‐crowned Night Nyctanassa violacea G5 S2B SpF M Heron WATERFOWL American Black Duck Anas rubripes G5 S4B S5N Yr B HH American Coot Fulica americana SpFW American Wigeon Anas americana SpFW M Blue‐winged Teal Anas discors SpSF Bufflehead Bucephala albeola SpFW H Canada Goose Branta canadensis Yr ? Canvasback Aythya valisineria G5 S3 S4N SpF
    [Show full text]
  • Número De Registro: 2889
    MEMORIAS CARTELES Número de registro: 2889 Estructura genética comparada en poblaciones conservadas y perturbadas de Quercus castanea y Q. deserticola, en la cuenca de Cuitzeo, Michoacán. Acosta Gómez Carlos Alberto1, Cuevas Reyes Pablo2, Oyama Nakagawa Alberto Ken1, González Rodríguez Antonio1 1Centro de Investigaciones en Ecosistemas, UNAM, México, [email protected] 2Facultad de Biología, Universidad Michoacana de San Nicolás de Hidalgo Se estudiaron los niveles de variación y estructura genética en un encino rojo (Quercus castanea, sección Lobatae) y un encino blanco (Quercus deserticola, sección Quercus) en poblaciones conservadas y perturbadas dentro de la cuenca de Cuitzeo, Michoacán. En ambas especies se utilizaron seis loci de microsatélites nucleares altamente polimórficos. En el caso de Q. castanea se encontró que la heterocigoscidad promedio esperada fue muy similar entre poblaciones conservadas y perturbadas (He = 0.717 vs. 0.705), mientras que en Q. deserticola fue mayor en las poblaciones conservadas (He = 0.744 vs. 0.533). La diferenciación entre poblaciones fue muy baja pero significativa en ambas especies (FST = 0.03; P = 0.004 y FST = 0.06; P = 0.018, respectivamente para Q. castanea y Q. deserticola). Los resultados sugieren que algunas poblaciones podrían experimentar efectos negativos sobre la diversidad genética debidos a la perturbación, aunque en general estos pueden verse disminuidos por los altos niveles de flujo génico y conectividad a través de la dispersión de polen entre las poblaciones de encinos de la cuenca. Número de registro: 78988 La estructura genética poblacional de la palma Chamaedorea alternans (Wendl.) arecaceae en un ambiente fragmentado: la selva tropical de Los Tuxtlas, Veracruz, México Aguilar Amézquita Bernardo1, Oyama Nakagawa Ken Alberto2, Núñez Farfán Juan3, Peñaloza Ramírez Juan2, Pérez Nasser Nidia2 1Instituto de Ecología, UNAM, México.
    [Show full text]
  • Vesicular Stomatitis Virus Enables Gene Transfer and Transsynaptic Tracing in a Wide Range of Organisms
    RESEARCH ARTICLE Vesicular Stomatitis Virus Enables Gene Transfer and Transsynaptic Tracing in a Wide Range of Organisms Nathan A. Mundell,1,2 Kevin T. Beier,1,2 Y. Albert Pan,3 Sylvain W. Lapan,1,2 Didem Goz€ Ayturk,€ 1,2 Vladimir K. Berezovskii,4 Abigail R. Wark,1 Eugene Drokhlyansky,1,2 Jan Bielecki,5 Richard T. Born,4 Alexander F. Schier,3 and Constance L. Cepko1,2* 1Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115 2Department of Ophthalmology, Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115 3Department of Molecular and Cellular Biology and Center for Brain Science, Harvard University, Cambridge, Massachusetts 01238 4Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115 5Department of Ecology, Evolution and Marine Biology, University of California, Santa Barbara, Santa Barbara, California 93106 Current limitations in technology have prevented an connections, and revealed several potentially novel con- extensive analysis of the connections among neurons, nections. Further, these vectors were shown to infect particularly within nonmammalian organisms. We devel- neurons in several other vertebrates, including Old and oped a transsynaptic viral tracer originally for use in New World monkeys, seahorses, axolotls, and Xenopus. mice, and then tested its utility in a broader range of They were also shown to infect two invertebrates, Dro- organisms. By engineering the vesicular stomatitis virus sophila melanogaster, and the box jellyfish, Tripedalia cys- (VSV) to encode a fluorophore and either the rabies virus tophora, a species previously intractable for gene glycoprotein (RABV-G) or its own glycoprotein (VSV-G), transfer, although no clear evidence of transsynaptic we created viruses that can transsynaptically label neuro- spread was observed in these species.
    [Show full text]
  • Vesicular Stomatitis Virus Enables Gene Transfer and Transsynaptic Tracing in a Wide Range of Organisms
    RESEARCH ARTICLE Vesicular Stomatitis Virus Enables Gene Transfer and Transsynaptic Tracing in a Wide Range of Organisms Nathan A. Mundell,1,2 Kevin T. Beier,1,2 Y. Albert Pan,3 Sylvain W. Lapan,1,2 Didem Goz€ Ayturk,€ 1,2 Vladimir K. Berezovskii,4 Abigail R. Wark,1 Eugene Drokhlyansky,1,2 Jan Bielecki,5 Richard T. Born,4 Alexander F. Schier,3 and Constance L. Cepko1,2* 1Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115 2Department of Ophthalmology, Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115 3Department of Molecular and Cellular Biology and Center for Brain Science, Harvard University, Cambridge, Massachusetts 01238 4Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115 5Department of Ecology, Evolution and Marine Biology, University of California, Santa Barbara, Santa Barbara, California 93106 Current limitations in technology have prevented an connections, and revealed several potentially novel con- extensive analysis of the connections among neurons, nections. Further, these vectors were shown to infect particularly within nonmammalian organisms. We devel- neurons in several other vertebrates, including Old and oped a transsynaptic viral tracer originally for use in New World monkeys, seahorses, axolotls, and Xenopus. mice, and then tested its utility in a broader range of They were also shown to infect two invertebrates, Dro- organisms. By engineering the vesicular stomatitis virus sophila melanogaster, and the box jellyfish, Tripedalia cys- (VSV) to encode a fluorophore and either the rabies virus tophora, a species previously intractable for gene glycoprotein (RABV-G) or its own glycoprotein (VSV-G), transfer, although no clear evidence of transsynaptic we created viruses that can transsynaptically label neuro- spread was observed in these species.
    [Show full text]
  • Q Feral Swine Survey
    Q Or. FERAL SWINE SURVEY - REGION 4 j t-• INTRODUCTION: •- : .-', :-,) \ In response to questions raised by Region 4 refuge managers conceriihgMe-impact ox feral swine on Southeastern refuges, a survey was developed to obtain the desired information. The survey form (Appendix A) included questions designed to assess the distribution, abundance and damage caused by feral swine on Region 4 refuges. Information was also requested on types and effectiveness of control methods. Survey forms were mailed to all Region 4 refuges with a two week response deadline. After two weeks, a second mailing was made to all refuges that had not responded. A total of 66 refuges from Region 4 responded to the survey. iGi- %r. 1TT0 •fi-Sst. K^ ~—=-A~««, Off. s. RESULTS AND DISCUSSION: Pile The raw data obtained from the questionnaire are shown on the summary sheet in Appendix A. Basically, approximately two-thirds of refuges reported feral swine populations on the refuge and/or on surrounding lands (61% and 70% respectively). Of those reporting swine present, 40 of 42 (95%) assessed the populations as stable or increasing while only 2 (5%) felt that populations were decreasing. Primary to the survey was the Managers' assessment of the extent of damage caused by feral swine. Twenty-five of 53 (47%) assessed hog damage as either significant or severe. Related damages included habitat/crop damage, competition with native wildlife, levee and road damage, erosion problems, threatened and endangered species depredation, diseases, and numerous other incidental impacts. These include reduction of oak regeneration, killing of trees by rubbing, and interference at bait sites for waterfowl banding.
    [Show full text]