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- W1991402451 abstract "Previous articleNext article No AccessNotes and CommentsPhenotypic Manipulation by the Cestode Parasite Schistocephalus solidus of Its Intermediate Host, Gasterosteus aculeatus, the Threespine SticklebackCarl P. LoBue and Michael A. BellCarl P. LoBue Search for more articles by this author and Michael A. Bell Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 142, Number 4Oct., 1993 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/285568 Views: 24Total views on this site Citations: 61Citations are reported from Crossref Copyright 1993 The University of ChicagoPDF download Crossref reports the following articles citing this article:Francis E. Tillman, James S. Adelman Searching while sick: How does disease affect foraging decisions and contact rates?, Functional Ecology 37, no.44 (Nov 2022): 838–844.https://doi.org/10.1111/1365-2435.14207Verônica Angélica Alves, Nadia Aubin‐Horth Implication of the myo ‐inositol pathway in behavioural alterations of infected threespine sticklebacks, Functional Ecology 37, no.44 (Nov 2022): 873–885.https://doi.org/10.1111/1365-2435.14216Jan Baer, Sarah M. Gugele, Samuel Roch, Alexander Brinker Stickleback mass occurrence driven by spatially uneven parasite pressure? Insights into infection dynamics, host mortality, and epizootic variability, Parasitology Research 121, no.66 (Apr 2022): 1607–1619.https://doi.org/10.1007/s00436-022-07517-4Megan A. Hahn, Agnes Piecyk, Fátima Jorge, Robert Cerrato, Martin Kalbe, Nolwenn M. Dheilly Host phenotype and microbiome vary with infection status, parasite genotype, and parasite microbiome composition, Molecular Ecology 31, no.55 (Jan 2022): 1577–1594.https://doi.org/10.1111/mec.16344B. Ruehle, O. Seppälä Manipulation of fish phenotype by parasites, (Jan 2022).https://doi.org/10.1016/B978-0-323-90801-6.00014-8Agnes Piecyk, Megan A. Hahn, Olivia Roth, Nolwenn M. Dheilly, David C. Heins, Michael A. Bell, Martin Kalbe Cross-continental experimental infections reveal distinct defence mechanisms in populations of the three-spined stickleback Gasterosteus aculeatus, Proceedings of the Royal Society B: Biological Sciences 288, no.19591959 (Sep 2021): 20211758.https://doi.org/10.1098/rspb.2021.1758Lucie Grecias, Francois Olivier Hebert, Verônica Angelica Alves, Iain Barber, Nadia Aubin-Horth Host behaviour alteration by its parasite: from brain gene expression to functional test, Proceedings of the Royal Society B: Biological Sciences 287, no.19381938 (Nov 2020): 20202252.https://doi.org/10.1098/rspb.2020.2252Karin Kjernsmo, Miranda Grönholm, Sami Merilaita Size and contrast increase the divertive effect of eyespots, Behavioral Ecology 30, no.11 (Oct 2018): 159–165.https://doi.org/10.1093/beheco/ary149David C. Heins, Kristine N. Moody, Sophia Miller , Parasitology 146, no.11 ( 2019): 97.https://doi.org/10.1017/S003118201800094XLucie Grécias, Julie Valentin, Nadia Aubin-Horth Testing the parasite mass burden effect on alteration of host behaviour in the Schistocephalus –stickleback system, Journal of Experimental Biology 221, no.66 (Mar 2018).https://doi.org/10.1242/jeb.174748Anna K Rahn, Simon Vitt, Lisa Drolshagen, Jörn P Scharsack, Ingolf P Rick, Theo C M Bakker Parasitic infection of the eye lens affects shoaling preferences in three-spined stickleback, Biological Journal of the Linnean Society 123, no.22 (Dec 2017): 377–387.https://doi.org/10.1093/biolinnean/blx155Marc Ritter, Martin Kalbe, Tina Henrich Virulence in the three-spined stickleback specific parasite Schistocephalus solidus is inherited additively, Experimental Parasitology 180 (Sep 2017): 133–140.https://doi.org/10.1016/j.exppara.2017.02.016I. Barber, A.B. Mora, E.M. Payne, K.L. Weinersmith, A. Sih Parasitism, personality and cognition in fish, Behavioural Processes 141 (Aug 2017): 205–219.https://doi.org/10.1016/j.beproc.2016.11.012Manuel Talarico, Franziska Seifert, Josef Lange, Norbert Sachser, Joachim Kurtz, Jörn P. Scharsack Specific manipulation or systemic impairment? Behavioural changes of three-spined sticklebacks (Gasterosteus aculeatus) infected with the tapeworm Schistocephalus solidus, Behavioral Ecology and Sociobiology 71, no.22 (Jan 2017).https://doi.org/10.1007/s00265-017-2265-9Lucie Grécias, François Olivier Hébert, Chloé Suzanne Berger, Iain Barber, Nadia Aubin-Horth Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology?, Journal of Experimental Biology 220, no.22 (Jan 2017): 237–246.https://doi.org/10.1242/jeb.151456Martin Kalbe, Christophe Eizaguirre, Jörn P. Scharsack, Per J. Jakobsen Reciprocal cross infection of sticklebacks with the diphyllobothriidean cestode Schistocephalus solidus reveals consistent population differences in parasite growth and host resistance, Parasites & Vectors 9, no.11 (Mar 2016).https://doi.org/10.1186/s13071-016-1419-3D. C. Heins, D. M. Eidam, J. A. Baker , Journal of Parasitology 102, no.22 ( 2016): 286.https://doi.org/10.1645/14-675C Lagrue, K Heaphy, B Presswell, R Poulin Strong association between parasitism and phenotypic variation in a supralittoral amphipod, Marine Ecology Progress Series (Jan 2016).https://doi.org/10.3354/meps11752Jolanta Morozińska-Gogol Changes in the parasite communities as one of the potential causes of decline in abundance of the three-spined sticklebacks in the Puck Bay, Oceanologia 57, no.33 (Jul 2015): 280–287.https://doi.org/10.1016/j.oceano.2015.03.001B. S. Harmon, R. Hilborn, T. P. Quinn Infection by the cestode parasite Schistocephalus sp. and effects on diet, body condition and survival of sculpins Cottus aleuticus and Cottus cognatus, Journal of Fish Biology 86, no.55 (Mar 2015): 1621–1629.https://doi.org/10.1111/jfb.12646Thomas Kuhn, Regina Klapper, Julian Münster, Dorian D. Dörge, Judith Kochmann, Sven Klimpel Remote Control: Parasite Induced Phenotypic Changes in Fish, (Jan 2015): 117–148.https://doi.org/10.1007/978-3-319-22936-2_9Nina Hafer, Manfred Milinski Cooperation or Conflict: Host Manipulation in Multiple Infections, (Jan 2015): 49–68.https://doi.org/10.1007/978-3-319-22936-2_4David C. Heins, Kelly A. Barry, Laura A. Petrauskas Consistency of host responses to parasitic infection in the three-spined stickleback fish infected by the diphyllobothriidean cestode Schistocephalus solidus, Biological Journal of the Linnean Society 113, no.44 (Oct 2014): 958–968.https://doi.org/10.1111/bij.12392DAVID C. HEINS, JOHN A. BAKER Fecundity compensation and fecundity reduction among populations of the three-spined stickleback infected by Schistocephalus solidus in Alaska, Parasitology 141, no.88 (Apr 2014): 1088–1096.https://doi.org/10.1017/S0031182014000535Janice Moore An overview of parasite-induced behavioral alterations – and some lessons from bats, Journal of Experimental Biology 216, no.11 (Jan 2013): 11–17.https://doi.org/10.1242/jeb.074088DAVID C. HEINS Fecundity compensation in the three-spined stickleback Gasterosteus aculeatus infected by the diphyllobothriidean cestode Schistocephalus solidus, Biological Journal of the Linnean Society 106, no.44 (May 2012): 807–819.https://doi.org/10.1111/j.1095-8312.2012.01907.xA Confer, V Vu, C. J. Drevecky, W. E. Aguirre Occurrence of Schistocephalus solidus in Anadromous Threespine Stickleback, Journal of Parasitology 98, no.33 (Jun 2012): 676–678.https://doi.org/10.1645/GE-2968.1T. P. Quinn, N. W. Kendall, H. B. Rich, B. E. Chasco Diel vertical movements, and effects of infection by the cestode Schistocephalus solidus on daytime proximity of three-spined sticklebacks Gasterosteus aculeatus to the surface of a large Alaskan lake, Oecologia 168, no.11 (Jul 2011): 43–51.https://doi.org/10.1007/s00442-011-2071-4Robert Poulin, Christopher A. Blanar, David. W. Thieltges, David J. Marcogliese The biogeography of parasitism in sticklebacks: distance, habitat differences and the similarity in parasite occurrence and abundance, Ecography 34, no.44 (Apr 2013): 540–551.https://doi.org/10.1111/j.1600-0587.2010.06826.xNicole Nishimura, David C. Heins, Ryan O. Andersen, Iain Barber, William A. Cresko, Howard Browman Distinct Lineages of Schistocephalus Parasites in Threespine and Ninespine Stickleback Hosts Revealed by DNA Sequence Analysis, PLoS ONE 6, no.77 (Jul 2011): e22505.https://doi.org/10.1371/journal.pone.0022505David C. Heins, John A. Baker, Dillon M. Green Processes Influencing the Duration and Decline of Epizootics in Schistocephalus solidus, Journal of Parasitology 97, no.33 (Jun 2011): 371–376.https://doi.org/10.1645/GE-2699.1O. Seppälä BEHAVIORAL RESPONSES TO THE ENVIRONMENT | Manipulation of Fish Phenotype by Parasites, (Jan 2011): 777–782.https://doi.org/10.1016/B978-0-12-374553-8.00138-6J. Dziekońska-Rynko, E. Dzika The tapeworm Paradilepis scolecina (Rudolphi, 1819) (Cestoda: Cyclophyllidea) invasion in Great Cormorant [Phalacrocorax carbo sinensis (Blumenbach, 1798)] from the breeding colony in Lake Selment Wielki (northern Poland), Helminthologia 48, no.11 (Jan 2011).https://doi.org/10.2478/s11687-011-0005-7D. C. HEINS, E. L. BIRDEN, J. A. BAKER Host mortality and variability in epizootics of Schistocephalus solidus infecting the threespine stickleback, Gasterosteus aculeatus, Parasitology 137, no.1111 (Jun 2010): 1681–1686.https://doi.org/10.1017/S003118201000048XDAVID C. HEINS, JOHN A. BAKER, MELISSA A. TOUPS, EMILY L. BIRDEN Evolutionary significance of fecundity reduction in threespine stickleback infected by the diphyllobothriidean cestode Schistocephalus solidus, Biological Journal of the Linnean Society 100, no.44 (Jul 2010): 835–846.https://doi.org/10.1111/j.1095-8312.2010.01486.xI. BARBER, J. P. SCHARSACK The three-spined stickleback- Schistocephalus solidus system: an experimental model for investigating host-parasite interactions in fish, Parasitology 137, no.33 (Oct 2009): 411–424.https://doi.org/10.1017/S0031182009991466Katrin Hammerschmidt, Joachim Kurtz Chapter 5 Ecological Immunology of a Tapeworms' Interaction with its Two Consecutive Hosts, (Jan 2009): 111–137.https://doi.org/10.1016/S0065-308X(08)00605-2Iain Barber, Ben Rushbrook Parasites and Fish Behaviour, (Feb 2014): 525–561.https://doi.org/10.1201/b10757-19I. Barber The Role of Parasites in Fish-Bird Interactions: A Behavioural Ecological Perspective, (Nov 2007): 221–243.https://doi.org/10.1002/9780470995372.ch17Iain Barber Parasites, behaviour and welfare in fish, Applied Animal Behaviour Science 104, no.3-43-4 (May 2007): 251–264.https://doi.org/10.1016/j.applanim.2006.09.005M.I. Sánchez, B.B. Georgiev, A.J. Green Avian cestodes affect the behaviour of their intermediate host Artemia parthenogenetica: An experimental study, Behavioural Processes 74, no.33 (Mar 2007): 293–299.https://doi.org/10.1016/j.beproc.2006.11.002Eric T. Schultz, Michelle Topper, David C. Heins Decreased reproductive investment of female threespine stickleback Gasterosteus aculeatus infected with the cestode Schistocephalus solidus: parasite adaptation, host adaptation, or side effect?, Oikos 114, no.22 (Mar 2006): 303–310.https://doi.org/10.1111/j.2006.0030-1299.14691.xOtto Seppälä, Anssi Karvonen, E. Tellervo Valtonen Impaired crypsis of fish infected with a trophically transmitted parasite, Animal Behaviour 70, no.44 (Oct 2005): 895–900.https://doi.org/10.1016/j.anbehav.2005.01.021Iain Barber, Hazel A. Wright Effects of Parasites on Fish Behaviour: Interactions With Host Physiology, (Jan 2005): 109–149.https://doi.org/10.1016/S1546-5098(05)24004-9David C Heins, Britt Ulinski, Jill Johnson, John A Baker Effect of the cestode macroparasite Schistocephalus pungitii on the reproductive success of ninespine stickleback, Pungitius pungitius, Canadian Journal of Zoology 82, no.1111 (Nov 2004): 1731–1737.https://doi.org/10.1139/z04-171David C. Heins, John A. Baker REDUCTION OF EGG SIZE IN NATURAL POPULATIONS OF THREESPINE STICKLEBACK INFECTED WITH A CESTODE MACROPARASITE, Journal of Parasitology 89, no.11 (Feb 2003): 1–6.https://doi.org/10.1645/0022-3395(2003)089[0001:ROESIN]2.0.CO;2David C. Heins, John A. Baker, Hillery C. Martin THE “CROWDING EFFECT” IN THE CESTODE SCHISTOCEPHALUS SOLIDUS: DENSITY-DEPENDENT EFFECTS ON PLEROCERCOID SIZE AND INFECTIVITY, Journal of Parasitology 88, no.22 (Apr 2002): 302–307.https://doi.org/10.1645/0022-3395(2002)088[0302:TCEITC]2.0.CO;2R Poulin, E.T Valtonen Interspecific associations among larval helminths in fish, International Journal for Parasitology 31, no.1414 (Dec 2001): 1589–1596.https://doi.org/10.1016/S0020-7519(01)00276-4Øyvind Øverli, Miklós Páll, Bertil Borg, Malcolm Jobling, Svante Winberg Effects of Schistocephalus solidus infection on brain monoaminergic activity in female three-spined sticklebacks Gasterosteus aculeatus, Proceedings of the Royal Society of London. Series B: Biological Sciences 268, no.14741474 (Jul 2001): 1411–1415.https://doi.org/10.1098/rspb.2001.1668T. E. REIMCHEN, P. NOSIL Ecological causes of sex-biased parasitism in threespine stickleback, Biological Journal of the Linnean Society 73, no.11 (Jan 2008): 51–63.https://doi.org/10.1111/j.1095-8312.2001.tb01346.xGregory J. Sandland, Cameron P. Goater PARASITE-INDUCED VARIATION IN HOST MORPHOLOGY: BRAIN-ENCYSTING TREMATODES IN FATHEAD MINNOWS, Journal of Parasitology 87, no.22 (Apr 2001): 267–272.https://doi.org/10.1645/0022-3395(2001)087[0267:PIVIHM]2.0.CO;2T E Reimchen, P Nosil Dietary differences between phenotypes with symmetrical and asymmetrical pelvis in the stickleback Gasterosteus aculeatus, Canadian Journal of Zoology 79, no.33 (Mar 2001): 533–539.https://doi.org/10.1139/z01-006Rodrigo Medel Assessment of correlational selection on tolerance and resistance traits in a host plant–parasitic plant interaction, Evolutionary Ecology 15, no.11 (Jan 2001): 37–52.https://doi.org/10.1023/A:1011966329939David C Heins, Scarlet S Singer, John A Baker Virulence of the cestode Schistocephalus solidus and reproduction in infected threespine stickleback, Gasterosteus aculeatus, Canadian Journal of Zoology 77, no.1212 (Dec 1999): 1967–1974.https://doi.org/10.1139/z99-180R. Poulin, F. 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