Giemsa Stain As a Marker in the Pitcher-Plant Mosquito, Wyeomyia Smithii

Total Page:16

File Type:pdf, Size:1020Kb

Giemsa Stain As a Marker in the Pitcher-Plant Mosquito, Wyeomyia Smithii 654 JouRr.uLoF THEAtr{snIclr.l Mosqurro CoNrRor,Assocrluox Vol. 7, No. 4 GIEMSA STAIN AS A MARKER IN THE PITCHER-PLANT MOSQUITO, WYEOMYIA SMITHII CHERYL A. KLECKNER AND WILLIAM E. BRADSHAW Depdrtment of Biology, Uniuersity of Oregon,Eugene, OR 97403 ABSTRACT. Third and fourth instars of Wyeomyia srnithii were reared in Giemsa stain at 4 concentrationsbetween 4 x 10-?and 10*5g/liter. The mosquitoesretained the blue mark as adults and remainedmarked throughout their laboratory life. Concentration of Giemsasignificantly affectedeclosion successbut had no significant effect on mean days to pupation or days as a pupa, male or female adult longevity, per-capita female fecundity or fertility. Larval exposureto low concentrations (4 x 10-7 or 10-" g/liter) of Giemsa stain provides an effective lifetime tag for otherwise indistinguishable laboratory populations. We undertook this study of Wyeomyinsmithii eclosionwas recordedby removing and sexing (Coq.)to determinewhether Giemsa stain would the pupal exuviae. Adults had constant access be an effective,easily detectablemarker for this to raisins and a cut leaf of their host plant, mosquito in laboratory populations. A reliable Sarraceniapurpured Linn., in a 70-ml glassjar marker for Wy. smithii would allow us to deter- half-filled with distilled water. The bottom of mine relative longevity of adults from distinct the cage was lined with filter paper kept moist populations when placed in mixed population with distilled water. cages receiving different treatments, Experi- We conducted 2 experiments. In the first, ments were designed to reveal the effect of within one day ofeclosion, adults were squashed Giemsa concentration,experienced during de- betweenslide and coverslip,sexed and examined velopment from larval diapauseto pupation, on against a white background under a dissecting adult eclosion success,longevity, fecundity, fer- microscope (15-30x magnification) for the tility and persistenceof the marker in the adults. Giemsastain. In this experiment 2 trials of third Overwintering larvae of Wyeomyia smithii instars were run at each of the 4 concentrations; (June were collectedin Maine 1988)and main- trials of fourth instars consisted of 2 replicates tained in the Iaboratory for 3 generations.Third each at concentrations of 10-6 and 4 x 10-u gl instar diapausewas induced by a short-day pho- liter and one trial each at 4 X 10-? and 10-5 (L:D : + toperiod 8:16) at 21 0.5"C and main- Giemsaconcentration. In the secondexperiment tained for 6 months prior to experiments.Larvae the adults remained in the cagesand were main- which molted to the fourth instar and the third tained until all adults had died. All dead adults instars were compared in 2 experiments. were removed daily, squashed,sexed and exam- The Giemsastain was preparedby adding the ined for the blue marker using a dissecting mi- appropriate amount of Giemsa powder (Fisher croscope.Eggs were removed from leaf and jar, ScientificCo., Pittsburgh,PA) to 1 liter of dis- pupal paper liner, tilled water and heating to ensure dissolution. dish and rinsed into distilled petri We tested 4 concentrationsof Giemsa stain: water in a 150 x 25 mm dish and counted. larvae were removed from the diapause regime Eggswere kept for 10 daysand all hatchedlarvae and placedin Giemsa(4 x 10-?,10-6, 4 x 10-6, were counted. Trials consistedof 2 replicates of and 10-5 g Giemsa/liter) solution. Experiments third instars in each of the 4 Giemsaconcentra- were conductedwith a daily sine-wavethermo- tions and in distilled water (controls); fourth period(12-28'C, mean :2t"C),80% RH anda instar trials included 2 replicatesat 4 x 10-6and long-dayphotoperiod (L:D = 18:6).Replicates at 10-6g/Iiter, one trial at 4 x l0-1 and at 10-5 of 30 larvae in 125 ml of Giemsasolution per g/liter Giemsaconcentration, and 2 control rep- petri dish were compared with controls reared licatesin distilled water. in distilled water. Larvae were fed (3 times/wk) Frequencieswere evaluated using the G-test an emulsion of guinea pig chow and freeze-dried for independence(Sokal and Rohlf 1969).Data brine shrimp (3:1 by volume). When cleaning were analyzedwith the nonparametric Kruskal- was necessaryfresh Giemsa solution was added Wallis test (SAS Institute 1985). to maintain a constantconcentration. The Giemsa marker was easily observed by Pupaewere collectedevery Monday, Wednes- using the technique describedabove. In the first day and Friday, transferred to plastic dessert experiment where the adults were examined on disheshalf-filled with unstained, distilled water the day of emergence,the blue Giemsastain was and placed in cylindrical screenedcages (200 x readily visible in L00Voof the individuals that 150 mm) in the same room as the larvae. Adult had been exposedto the stain as larvae, regard- DECEMBER1991 OpnRarroNar,ero ScroNrruc NorES Iessof concentration. In the secondexperiment, mean adult longevity ranged from 5.5 to 17.0 days. The blue Giemsa marker persisted throughout the adult life span in 100% of the individuals that had been exposedto the stain as larvae, regardlessof concentration, but was z not visible in any ofthe unexposedcontrols. a The concentration of Giemsasignificantly af- 9ro fected eclosion success(G with a df: 8L.46;P O < 0.001) (Fig. 1). The Kruskal-Wallis test (x' t! with 4 df) showedno significant effect of Giemsa concentration on mean days to pupation (12 : 5.35;P > 0.05) or days as a pupa (X2: 2.31;P > 0.05)(Table 1). Similarly, the Kruskal-Wallis G:81.a6 test showedno significant effect of Giemsacon- P <0.001 centration on longevity of adult males (12 : 4.13;P > 0.05)or females(x' : 7.73;P > 0.05), o 4 10 40 100 per-capitafemale fecundity (x' : 6.13;P > 0.05) or fertility (x' :6.55; P > 0.05). GIEMSACONCENTRATION X 1O-7GILITER In our study, long exposureof 2-4 wk during Fig. 1. Eclosionsuccess of Wyeomyiasmithii pupae larval development effectively marked Wyeo- exposedto Giemsastain as third (O) and fourth (O) rnyia smithii larvae. At low concentrations (4 X instars,including controls (0 g/liter).Concentration 10-7and 10-6g/liter) the dye affects emergence of Giemsasignificantly affected eclosion (P < 0.001). minimally and yet produces 100% marking that persists throughout adult lifetime. The stain also has a minimal effect on life history char- indicated that some growth retardation was ev- acters of Wy. stnithii. Previous studies (Weath- ident in the treated larvae. Our studies show no ersbeeand Hasell 1938,Haddow 1942,Joslyn et significant effects of Giemsa concentration on al. 1985,Joslyn and Fish 1986,Kay and Mot- developmenttime or on longevity, fecundity or tram L986) with Giemsa did not investigate the fertility of adult Wy. smithii. However, as shown effects of the procedure on longevity, fecundity in Table 1, there were parallel (albeit nonsig- or fertility of the treated adults. Weathersbee nificant) rises in larval development times and and Hasell (1938)and Kay and Mottram (1986) declines in male and female longevity, female Table 1. Life-history parametersof Wyeomyiasmithii exposedto different concentrations of Giemsa stain, including controls reared in distilled water (0 g/liter). Values are parameter means. t0 40 100 x'(K-w)* Days to pupation D.JA 3rd instar 22 26 26 30 29 4th instar 19 20 18 20 24 Days as pupa 2.31 3rd instar 87887 4th instar 798qE Male longevity (days) 4.r3 3rd instar 10 10 t2 66 4th instar t2 16 12 10# Femalelongevity (days) 3rd instar 13 15 13 10 11 4th instar 14 L7 12 10# Fecundity (eggsfemale) 6.13 3rd instar 46 34 17 17 4th instar 48 34 60 0# Fertility (%hatnh) 6.55 3rd instar 93 92 79 00 4th instar 99 75 100 0# f No adults eclosedfrom these treatments. * Kruskal-Wallis test for equality of Giemsa effects;with 4 df minimum significant (P < 0.0S)x2 = g.4g. 656 JounNer,oF THE AunRrcex Mosqurro CoNrRoLAssocrarroN Vor. ?,No. 4 fecundity and egg hatchability among mosqui- purea,pp.161-189. In: J. H. Frank and L. P. Loun- toes which had been exposed as larvae to a ibos (eds.),Phytotelmata: terrestrial plants as hosts Giemsaconcentration greater than 10-6 g/liter. for aquatic insect communities. Plexus Publ., Med- We would therefore caution against long expo- ford, NJ. Bradshaw, sures to higher than 10-6 g/liter Giemsa. Used W. E. and C. M. Holzapfel.1983. Predator- mediated, non-equilibrium coexistenceof tree-hole judiciously, prolonged exposure to low concen- mosquitoesin southeasternNorth America. Oecol- trations of Giemsa can provide a good tag for ogia 57:239-256. laboratory populations of. Wyeornyia srnithii Copeland,R. S. and G. B. Craig, Jr. 1990.Habitat which are otherwise indistinguishable as adults. segregationamong treehole mosquitoes(Diptera: Although our experiments were not designed Culicidae) in the Great Lakes region of the United to test field use, the Giemsa self-marking tech- States.Ann. Entomol. Soc.Am. 83:1063-1073. nique has potential field applicability. An effec- Haddow,A. J.1942. The mosquitofauna and climate tive field marker would aid in dispersal studies. of native huts at Kisumu, Kenya. Bull. Entomol. Res.33:91-142. Giemsa stain could be used to determine which Joslyn, D. J., L. B. Conrad and P. T. Slavin. 1985. individual adult mosquitoesemerge from differ- Development and preliminary field testing of the ent speciesof pitcher plants (Bradshaw 1983)or Giemsa self-marker for the salt marsh mosquito different sub-habitats among tree hole mosqui- Aedessollicitans (Walker) (Diptera:Culicidae). Ann. toes (e.g.,Bradshaw and Holzapfel 1983,Cope- Entomol. Soc. Am. 78.,20-23. land and Craig 1990). Joslyn, D. J. and D. Fish. 1986.Adult dispersalof We thank Christina Holzapfel, Jeffrey J. Aedescomrnums using Giemsa self-marking. J. Am. Hard, Sam Donovan and John M.
Recommended publications
  • A Five-Year Research Program Is Proposed to Expand the Theory of Community Assembly from Its Current Base of Correlative Inferen
    PROJECT SUMMARY A five-year research program is proposed to expand the theory of community assembly from its current base of correlative inferences to one grounded in process-based conclusions derived from controlled field and laboratory experiments. Northern pitcher plants, Sarracenia purpurea, and their community of inquiline arthropods and rotifers, will be used as the model system for the proposed experiments. There are three goals to the proposed research. (1) Inquiline assemblages that colonize pitcher plants will be developed as a model system for understanding community assembly and persistence. (2) Field and laboratory experiments will be used to elucidate causes of inquiline community colonization, assembly, and persistence, and the consequences of inquiline community dynamics for plant leaf allocation patterns, growth, and reproduction, as well as within-plant nutrient cycling. Reciprocal interactions of plant dynamics on inquiline community structure will also be investigated experimentally. (3) Matrix models will be developed to describe reciprocal interactions between inquiline community assembly and persistence, and inquilines’ living host habitats. As an integrated whole, the proposed experiments and models will provide a complete picture of linkages between pitcher-plant inquiline communities and their host plants, at individual leaf and whole-plant scales. This focus on measures of plant performance will fill an apparent lacuna in prior studies of pitcher plant microecosystems, which, with few exceptions, have focused almost exclusively on inquiline population dynamics and interspecific interactions. Plant demography of S. purpurea will be described and modeled for the first time. Complementary, multi-year field and greenhouse experiments will reveal effects of soil and pitcher nutrient composition on leaf allocation, plant growth, and reproduction.
    [Show full text]
  • Wyeomyia Smithii
    Commonwealth of Massachusetts State Reclamation and Mosquito Control Board NORTHEAST MASSACHUSETTS MOSQUITO CONTROL AND WETLANDS MANAGEMENT DISTRICT Wyeomyia smithii Kimberly Foss- Entomologist 118 Tenney Street Georgetown, MA 01833 Phone: (978) 352-2800 www.northeastmassmosquito.org Morphological Characteristics • Larvae • Antennal setae 1-A single • Single row of comb scales • Siphon w/ numerous long single setae • Saddle incomplete w/o median ventral brush • Only 2 anal gills (contribute to cutaneous respiration or length of time submerged?) • Adult • Size similar to Ur. sapphirina • Proboscis dark scaled, unbanded • Occiput dark w/ metallic blue-green scales • Scutum dark brownish-gray metallic scales, mesopostnotum with setae • Abdominal terga dark w/ metallic sheen, sides of sterna pale-scaled • Legs dark-scaled, unbanded Photos: Maryland Biodiversity Distribution/ Habitat • Gulf Coast to Northern Canada (post glacial range expansion) • Acidic sphagnum bogs and fens • Commensalistic w/ carnivorous host plant • Northern or Purple Pitcher Plant (Sarracenia pupurea) • Shared habitat 2 diptera sp. (midge, flesh fly) • Presence assists in nutrient absorption Photos: Wikipedia Bionomics • Autogenus • Multivoltine • 2x per year -late spring & early fall • Some larvae in a generation will develop at different times • Some larvae will not pupate for 10 months • Weak flyers (~15 meters), very prone to desiccation • Females rest, feed and fly (other species do not) with hind legs bent forward over head Photo: NJ Mosquito Control Association
    [Show full text]
  • Proteomic Characterization of the Major Arthropod Associates of the Carnivorous Pitcher Plant Sarracenia Purpurea
    2354 DOI 10.1002/pmic.201000256 Proteomics 2011, 11, 2354–2358 DATASET BRIEF Proteomic characterization of the major arthropod associates of the carnivorous pitcher plant Sarracenia purpurea Nicholas J. Gotelli1, Aidan M. Smith1, Aaron M. Ellison2 and Bryan A. Ballif1,3 1 Department of Biology, University of Vermont, Burlington, VT, USA 2 Harvard Forest, Harvard University, Petersham, MA, USA 3 Vermont Genetics Network Proteomics Facility, University of Vermont, Burlington, VT, USA The array of biomolecules generated by a functioning ecosystem represents both a potential Received: April 19, 2010 resource for sustainable harvest and a potential indicator of ecosystem health and function. Revised: January 10, 2011 The cupped leaves of the carnivorous pitcher plant, Sarracenia purpurea, harbor a dynamic Accepted: February 28, 2011 food web of aquatic invertebrates in a fully functional miniature ecosystem. The energetic base of this food web consists of insect prey, which is shredded by aquatic invertebrates and decomposed by microbes. Biomolecules and metabolites produced by this food web are actively exchanged with the photosynthesizing plant. In this report, we provide the first proteomic characterization of the sacrophagid fly (Fletcherimyia fletcheri), the pitcher plant mosquito (Wyeomyia smithii), and the pitcher-plant midge (Metriocnemus knabi). These three arthropods act as predators, filter feeders, and shredders at distinct trophic levels within the S. purpurea food web. More than 50 proteins from each species were identified, ten of which were predominantly or uniquely found in one species. Furthermore, 19 peptides unique to one of the three species were identified using an assembled database of 100 metazoan myosin heavy chain orthologs.
    [Show full text]
  • The Maryland Entomologist
    THE MARYLAND ENTOMOLOGIST Volume 5, Number 1 September 2009 September 2009 The Maryland Entomologist Volume 5, Number 1 MARYLAND ENTOMOLOGICAL SOCIETY Executive Committee: President Frederick Paras Vice President Philip J. Kean Secretary Richard H. Smith, Jr. Treasurer Edgar A. Cohen, Jr. Newsletter Editor Harold J. Harlan Journal Editor Eugene J. Scarpulla Historian Robert S. Bryant The Maryland Entomological Society (MES) was founded in November 1971, to promote the science of entomology in all its sub-disciplines; to provide a common meeting venue for professional and amateur entomologists residing in Maryland, the District of Columbia, and nearby areas; to issue a periodical and other publications dealing with entomology; and to facilitate the exchange of ideas and information through its meetings and publications. The MES logo features a drawing of a specimen of Euphydryas phaëton (Drury), the Baltimore Checkerspot, with its generic name above and its specific epithet below (both in capital letters), all on a pale green field; all these are within a yellow ring double-bordered by red, bearing the message “* Maryland Entomological Society * 1971 *”. All of this is positioned above the Shield of the State of Maryland. In 1973, the Baltimore Checkerspot was named the official insect of the State of Maryland through the efforts of many MES members. Membership in the MES is open to all persons interested in the study of entomology. All members receive the journal, The Maryland Entomologist, and the e-mailed newsletter, Phaëton. Institutions may subscribe to The Maryland Entomologist but may not become members. Prospective members should send to the Treasurer full dues for the current MES year, along with their full name, address, telephone number, entomological interests, and e-mail address.
    [Show full text]
  • Transcriptional Regulation of Mosquito Oogenesis Patrick David Jennings Iowa State University
    Iowa State University Capstones, Theses and Graduate Theses and Dissertations Dissertations 2011 Transcriptional regulation of mosquito oogenesis Patrick David Jennings Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/etd Part of the Entomology Commons Recommended Citation Jennings, Patrick David, "Transcriptional regulation of mosquito oogenesis" (2011). Graduate Theses and Dissertations. 12181. https://lib.dr.iastate.edu/etd/12181 This Thesis is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Transcriptional regulation of mosquito oogenesis by Patrick David Jennings A thesis submitted to the graduate faculty in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Major: Entomology Program of Study Committee: Lyric C. Bartholomay, Major Professor Bryony C. Bonning Bradley J. Blitvich Iowa State University Ames, Iowa 2011 Copyright © Patrick David Jennings, 2011. All rights reserved. ii TABLE OF CONTENTS LIST OF FIGURES iv LIST OF TABLES vi ABSTRACT vii CHAPTER 1. GENERAL INTRODUCTION 1 Introduction 1 Thesis Organization 3 Literature Review 4 Figures/Tables 13 References 15 CHAPTER 2. MOLECULAR MECHANISMS OF NUTRITIONAL SIGNALING DURING OOGENESIS IN AEDES TRISERIATUS 22 Abstract 22 Introduction 22 Materials and Methods 26 Results 30 Discussion 32 Acknowledgments 34 Figures/Tables 35 References 41 CHAPTER 3. AEDENOVO: A PIPELINE FOR DE NOVO TRANSCRIPT ASSEMBLY USING ORTHOLOGOUS GENES 45 Abstract 45 Introduction 45 Materials and Methods 49 Results 51 Discussion 52 Acknowledgments 53 Figures 54 References 57 CHAPTER 4.
    [Show full text]
  • Inquiline Diversity of the Purple Pitcher Plant (Sarracenia Purpurea) As a Function Of
    Inquiline diversity of the purple pitcher plant (Sarracenia purpurea) as a function of pitcher isolation: the role of dispersal in metacommunities BIOS 35502: Practicum in Field Biology Taylor Gulley Advisor: Michael Pfrender 2010 Gulley 2 “To understand the relative impact of any ecological process in structuring communities, it is essential to understand the spatial and temporal scale relevant for the particular question being addressed” (Addicott et al. 1987 as cited by Cáceres and Soluk 2002). Abstract: Increasing empirical evidence suggests that patterns of diversity depend on the spatial scale being observed. For example, local communities linked by dispersal (―metacommunities‖) are not only affected by those processes that operate within the community (such as predation and competition), but also by those that operate on a larger scale (such as migration between communities). The purple pitcher plant Sarracenia purpurea provides an ideal opportunity to explore the dynamics of metacommunities because of the discrete nature of the phytotelmata inhabited by a unique suite of easily manipulated aquatic organisms. Using methods inspired by Simberloff and Wilson’s study on the recolonization of seven islands in Florida Bay (1969- 1970), this study sought to determine the extent to which pitcher plant isolation affects the diversity of the inquiline community that can colonize it. It became clear, however, that such a study is premature; the dispersal mechanisms, rates, and range of distances of which inquilines are capable must be determined first. INTRODUCTION A primary goal of community ecology is to determine the patterns that shape the distribution, abundance, and interaction of species. Traditionally, community theory has focused on the processes that govern diversity on a local scale, assuming local habitats to be closed or isolated (Leibold et al.
    [Show full text]
  • Evolutionary Transition from Blood Feeding to Obligate Nonbiting in a Mosquito
    Evolutionary transition from blood feeding to obligate nonbiting in a mosquito William E. Bradshawa,1, Joshua Burkharta,b, John K. Colbournec, Rudyard Borowczaka, Jacqueline Lopezd,e, David L. Denlingerf,g,1, Julie A. Reynoldsf,g, Michael E. Pfrenderd,e, and Christina M. Holzapfela,1 aLaboratory of Evolutionary Genetics, Institute of Ecology and Evolution, University of Oregon, Eugene, OR 97403; bDepartment of Medical Informatics and Clinical Epidemiology, School of Medicine, Oregon Health and Science University, Portland, OR 97239; cSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom; dDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556; eEck Institute for Global Health, University of Notre Dame, Notre Dame, IN 46556; fDepartment of Entomology, The Ohio State University, Columbus, OH 43210; and gDepartment of Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, OH 43210 Contributed by David L. Denlinger, November 28, 2017 (sent for review October 6, 2017; reviewed by Walter S. Leal and L. Philip Lounibos) The spread of blood-borne pathogens by mosquitoes relies on their (DGE) as a direct consequence of selection on blood feeding within taking a blood meal; if there is no bite, there is no disease the polymorphic population to identify genes involved in the evolu- transmission. Although many species of mosquitoes never take a tionary transformation between blood-feeding and obligate nonbiting blood meal, identifying genes that distinguish blood feeding from populations within a single species in nature. obligate nonbiting is hampered by the fact that these different Among the known contemporary species of mosquitoes, only lifestyles occur in separate, genetically incompatible species.
    [Show full text]
  • Life History Characteristics of Wyeomyia Smithii from New Jersey
    Journal ofVector Ecology 24(1): 70-77 1 799H4 Life History Characteristics of Wyeomyia smithii from New Jersey Farida Mahmood and Wayne J. Crans Department of Entomology, Rutgers the State University 180 Jones Avenue, New Brunswick NJ 08901-8536 Received 29 July 1998; Accepted 72 October 1998 ABSTRACT: We colonized Wyeomyia smithii (Coquillett) from southern New Jersey and studied life history characteristics in the laboratory. Males and females showed no significant difference in time spent from first to third instar, but female larvae remained in fourth instar 2.1 days longer than males. At 22+/-2C females emerged 22.6+/-3 days after egg hatch; males emerged approximately two days earlier. Male emergence peaked five hours after dawn; females showed a trend to emerge late in the day. Rotation of male terminalia was completed 9 to 11 hours after emergence. Females were capable of mating immediately after emergence. Wyeomyia smithii females laid their first egg batch four to six days after emergence. Females were capable of laying up to seven batches ofeggs, however the mean number ofeggs per oviposition decreased significantly as the number of oviposition cycles increased. Keyword Index: Wyeomyia smithii, larval development, emergence rhythms, sexual maturation, fecundity. INTRODUCTION rates of females and males, diel emergence rhythms, sexual maturation of both sexes, ovarian development, Wyeomyia smithii (Coquillett) is distributed in and fecundity of females. eastern North America from the Gulf of Mexico to Labrador and northeastern Saskatchewan (Bradshaw MATERIALS AND METHODS and Holzapel 1996). The mosquito completes its immature development in aquatic habitat offered by the Colony Maintenance leaves of the purple pitcher plant, Sarracenia purpurea A colony of Wy.
    [Show full text]
  • Evolutionary Transition from Blood Feeding to Obligate Nonbiting in a Mosquito
    Evolutionary transition from blood feeding to obligate nonbiting in a mosquito William E. Bradshawa,1, Joshua Burkharta,b, John K. Colbournec, Rudyard Borowczaka, Jacqueline Lopezd,e, David L. Denlingerf,g,1, Julie A. Reynoldsf,g, Michael E. Pfrenderd,e, and Christina M. Holzapfela,1 aLaboratory of Evolutionary Genetics, Institute of Ecology and Evolution, University of Oregon, Eugene, OR 97403; bDepartment of Medical Informatics and Clinical Epidemiology, School of Medicine, Oregon Health and Science University, Portland, OR 97239; cSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom; dDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556; eEck Institute for Global Health, University of Notre Dame, Notre Dame, IN 46556; fDepartment of Entomology, The Ohio State University, Columbus, OH 43210; and gDepartment of Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, OH 43210 Contributed by David L. Denlinger, November 28, 2017 (sent for review October 6, 2017; reviewed by Walter S. Leal and L. Philip Lounibos) The spread of blood-borne pathogens by mosquitoes relies on their (DGE) as a direct consequence of selection on blood feeding within taking a blood meal; if there is no bite, there is no disease the polymorphic population to identify genes involved in the evolu- transmission. Although many species of mosquitoes never take a tionary transformation between blood-feeding and obligate nonbiting blood meal, identifying genes that distinguish blood feeding from populations within a single species in nature. obligate nonbiting is hampered by the fact that these different Among the known contemporary species of mosquitoes, only lifestyles occur in separate, genetically incompatible species.
    [Show full text]
  • Bulletin Number / Numéro 1 Entomological Society of Canada Société D’Entomologie Du Canada March / Mars 2018
    ............................................................ .......................................................... Volume 50 Bulletin Number / numéro 1 Entomological Society of Canada Société d’entomologie du Canada March / mars 2018 Published quarterly by the Entomological Society of Canada Publication trimestrielle par la Société d’entomologie du Canada ........................................................................................................... .......................................................................................................................................................... .......................................................................................................................................................... ................................................................................................................... ............................................................... .......................................................................... List of Contents / Table des matières Volume 50(1), March / mars 2018 Up front / Avant-propos ..........................................................................................................1 Joint Annual Meeting 2018 / Reunion annuelle conjointe 2018...............................................4 STEP Corner / Le coin de la relève............................................................................................5 People in the news / Gens qui font les manchettes.............................................................6
    [Show full text]
  • Predicting Food-Web Structure with Metacommunity Models
    University of Vermont ScholarWorks @ UVM College of Arts and Sciences Faculty Publications College of Arts and Sciences 4-1-2013 Predicting food-web structure with metacommunity models Benjamin Baiser Harvard University Hannah L. Buckley Lincoln University, New Zealand Nicholas J. Gotelli University of Vermont Aaron M. Ellison Harvard University Follow this and additional works at: https://scholarworks.uvm.edu/casfac Part of the Climate Commons Recommended Citation Baiser B, Buckley HL, Gotelli NJ, Ellison AM. Predicting food‐web structure with metacommunity models. Oikos. 2013 Apr;122(4):492-506. This Article is brought to you for free and open access by the College of Arts and Sciences at ScholarWorks @ UVM. It has been accepted for inclusion in College of Arts and Sciences Faculty Publications by an authorized administrator of ScholarWorks @ UVM. For more information, please contact [email protected]. i t o r ’ Oikos 122: 492–506, 2013 d s E doi: 10.1111/j.1600-0706.2012.00005.x OIKOS © 2012 The Authors. Oikos © 2012 Nordic Society Oikos Subject Editor: Carlos Melian. Accepted 10 July 2012 C h o i c e Predicting food-web structure with metacommunity models Benjamin Baiser, Hannah L. Buckley, Nicholas J. Gotelli and Aaron M. Ellison B. Baiser ([email protected]) and A. M. Ellison, Harvard Univ., Harvard Forest, 324 N. Main St., Petersham, MA 01366, USA. – H. L. Buckley, Dept of Ecology, PO Box 84, Lincoln Univ., Canterbury, New Zealand. – N. J. Gotelli, Dept of Biology, Univ. of Vermont, Burlington, VT 05405, USA­­. Metacommunity theory aims to elucidate the relative influence of local and regional-scale processes in generating diversity patterns across the landscape.
    [Show full text]
  • S-PLUS Graphics
    Trzcinski et al.: Local interactions in pitcher plant communities Environmental Entomology Section: Community and ecosystem ecology M. Kurtis Trzcinski Population Ecology Division Bedford Institute of Oceanography P.O. Box 1006 Phone: (902) 426-2298 Fax: (902) 426-1506 email: [email protected] Local interactions in pitcher plant communities scale-up to regional patterns in distribution and abundance 1 1 2 M. KURTIS TRZCINSKI, SANDRA J. WALDE, AND PHILIP D. TAYLOR 1 Department of Biology, Dalhousie University, Halifax, Nova Scotia, Canada, B3H 4J1 2Atlantic Cooperative Wildlife Ecology Research Network, Department of Biology, Acadia University, Wolfville, Nova Scotia, Canada, B0P 2N5 1 Abstract 2 We used the aquatic communities living in the purple pitcher plant (Sarracenia purpurea L., 3 Sarraceniaceae) to determine if patterns produced by trophic interactions at the local scale can be 4 detected at larger spatial scales. Mosquitoes (Wyeomyia smithii Coq., Diptera: Culicidae) are 5 known to have a negative effect on the aquatic microfauna within leaves. We compared the 6 abundance of two microfaunal taxa, Bodo (Kinetoplastea: Bodonidae), and Habrotrocha rosa 7 Donner (Rotifera: Bdelloidea), in bogs with and without pitcher-plant mosquitoes. Bogs 8 containing pitcher plant mosquitoes had lower densities of bacteria through the study period. 9 However, within these bogs, leaves with mosquitoes did not have lower bacterial densities. We 10 found that the pattern for Bodo was similar at the leaf and bog spatial scales. Abundance of Bodo 11 was closely linked to bacterial densities and the presence of mosquitoes strengthened that 12 relationship, due to greater predator impacts when bacteria were scarce.
    [Show full text]