Artigo Revisado por pares

Aphally Versus Euphally in Self-Fertile Hermaphrodite Snails from the Species Bulinus truncatus (Pulmonata: Planorbidae)

1992; University of Chicago Press; Volume: 139; Issue: 2 Linguagem: Inglês

10.1086/285335

ISSN

1537-5323

Autores

Philippe Jarne, Luc Finot, Christian Bellec, Bernard Delay,

Tópico(s)

Parasite Biology and Host Interactions

Resumo

Previous articleNext article No AccessNotes and CommentsAphally Versus Euphally in Self-Fertile Hermaphrodite Snails from the Species Bulinus truncatus (Pulmonata: Planorbidae)Philippe Jarne, Luc Finot, Christian Bellec, and Bernard DelayPhilippe Jarne Search for more articles by this author , Luc Finot Search for more articles by this author , Christian Bellec Search for more articles by this author , and Bernard Delay Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 139, Number 2Feb., 1992 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/285335 Views: 6Total views on this site Citations: 34Citations are reported from Crossref Copyright 1992 The University of ChicagoPDF download Crossref reports the following articles citing this article:J.R. Auld, P. Jarne Sex and Recombination in Snails, (Jan 2016): 49–60.https://doi.org/10.1016/B978-0-12-800049-6.00149-9Osama M.S. Mostafa, Saad M. Bin Dajem, Ahmed Al-Qahtani, Essam H. Ibrahim, Saleh A.S. Al-Quraishy Developing species-specific primers to identify Bulinus truncatus and Bulinus beccari, the intermediate hosts of Schistosoma haematobium in Saudi Arabia, Gene 499, no.22 (May 2012): 256–261.https://doi.org/10.1016/j.gene.2012.03.024Allen Nalugwa, Aslak Jørgensen, Silvester Nyakaana, Thomas K. Kristensen Genetic variation within and between populations of hermaphroditic Bulinus truncatus tetraploid freshwater snails of the Albertine Rift, East Africa, Hydrobiologia 673, no.11 (Jun 2011): 53–61.https://doi.org/10.1007/s10750-011-0749-6Juan S. Escobar, Josh R. Auld, Ana C. Correa, Juan M. Alonso, Yves K. Bony, Marie‐Agnès Coutellec, Joris M. Koene, Jean‐Pierre Pointier, Philippe Jarne, Patrice David PATTERNS OF MATING‐SYSTEM EVOLUTION IN HERMAPHRODITIC ANIMALS: CORRELATIONS AMONG SELFING RATE, INBREEDING DEPRESSION, AND THE TIMING OF REPRODUCTION, Evolution 65, no.55 (Jan 2011): 1233–1253.https://doi.org/10.1111/j.1558-5646.2011.01218.xKurt Jordaens, Stefan Van Dongen, Katrien Temmerman, Thierry Backeljau Resource allocation in a simultaneously hermaphroditic slug with phally polymorphism, Evolutionary Ecology 20, no.66 (Sep 2006): 535–548.https://doi.org/10.1007/s10682-006-9115-yMarie-Agnès Coutellec, Laurent Lagadic Effects of Self-Fertilization, Environmental Stress and Exposure to Xenobiotics on Fitness-Related Traits of the Freshwater Snail Lymnaea stagnalis, Ecotoxicology 15, no.22 (Jan 2006): 199–213.https://doi.org/10.1007/s10646-005-0049-xM.-F. Ostrowski, P. Jarne, P. David A phallus for free? Quantitative genetics of sexual trade-offs in the snail Bulinus truncatus, Journal of Evolutionary Biology 16, no.11 (Jan 2003): 7–16.https://doi.org/10.1046/j.1420-9101.2003.00508.xM-F Ostrowski, P Jarne, O Berticat, P David Ontogenetic reaction norm for binary traits: the timing of phallus development in the snail Bulinus truncatus, Heredity 88, no.55 (May 2002): 342–348.https://doi.org/10.1038/sj.hdy.6800049Flobert Njiokou, Jean Bosco Mouafo, Félicité Teukeng, Thomas Njine, Albert Same Ekobo, Philippe Jarne The influence of self-fertilization and pairing on life-history traits in the freshwater snail Bulinus forskalii (Gastropoda, Planorbidae), Acta Tropica 76, no.22 (Sep 2000): 159–167.https://doi.org/10.1016/S0001-706X(00)00073-5Marie-France Ostrowski, Philippe Jarne, Patrice David QUANTITATIVE GENETICS OF SEXUAL PLASTICITY: THE ENVIRONMENTAL THRESHOLD MODEL AND GENOTYPE-BY-ENVIRONMENT INTERACTION FOR PHALLUS DEVELOPMENT IN THE SNAIL BULINUS TRUNCATUS, Evolution 54, no.55 (Jan 2000): 1614.https://doi.org/10.1554/0014-3820(2000)054[1614:QGOSPT]2.0.CO;2Stephen C. Weeks, Vivien Marcus, Bobbi R. Crosser INBREEDING DEPRESSION IN A SELF‐COMPATIBLE, ANDRODIOECIOUS CRUSTACEAN, EULIMNADIA TEXANA, Evolution 53, no.22 (May 2017): 472–483.https://doi.org/10.1111/j.1558-5646.1999.tb03782.xK. Jordaens, T. Backeljau, P. Ondina, H. Reise, R. Verhagen Allozyme homozygosity and phally polymorphism in the land snail Zonitoides nitidus (Gastropoda, Pulmonata), Journal of Zoology 246, no.11 (Feb 2006): 95–104.https://doi.org/10.1111/j.1469-7998.1998.tb00137.xClaudie Doums, Frédérique Viard, Philippe Jarne The evolution of phally polymorphism, Biological Journal of the Linnean Society 64, no.33 (Jan 2008): 273–296.https://doi.org/10.1111/j.1095-8312.1998.tb00334.xClaudie Doums, Mireille-Ange Perdieu, Philippe Jarne RESOURCE ALLOCATION AND STRESSFUL CONDITIONS IN THE APHALLIC SNAIL BULINUS TRUNCATUS, Ecology 79, no.22 (Mar 1998): 720–733.https://doi.org/10.1890/0012-9658(1998)079[0720:RAASCI]2.0.CO;2Bruno Baur Sperm Competition in Molluscs, (Jan 1998): 255–305.https://doi.org/10.1016/B978-012100543-6/50033-7F. Viard, C. Doums, P. Jarne Selfing, sexual polymorphism and microsatellites in the hermaphrodititic freshwater snail Bulinus truncatus, Proceedings of the Royal Society of London. Series B: Biological Sciences 264, no.13781378 (Jan 1997): 39–44.https://doi.org/10.1098/rspb.1997.0006S. G. Johnson, C. M. Lively, S. J. Schrag Evolution and ecological correlates of uniparental and biparental reproduction in freshwater snails, (Jan 1997): 263–291.https://doi.org/10.1007/978-3-0348-8880-6_10Claudie Doums, Rabiou Labbo, Philippe Jarne Stability and genetic basis of variability of phally polymorphism in natural populations of the self-fertile freshwater snail Bulinus truncatus, Genetical Research 68, no.11 (Apr 2009): 23–33.https://doi.org/10.1017/S0016672300033851Claudie Doums, Philippe Jarne The evolution of phally polymorphism in Bulinus truncatus (Gastropoda, Planorbidae): the cost of male function analysed through life-history traits and sex allocation, Oecologia 106, no.44 (Jun 1996): 464–469.https://doi.org/10.1007/BF00329703S. J. Schrag, A. F. Read Loss of male outcrossing ability in simultaneous hermaphrodites: phylogenetic analyses of pulmonate snails, Journal of Zoology 238, no.22 (May 2009): 287–299.https://doi.org/10.1111/j.1469-7998.1996.tb05395.x Outcrossing rates and correlated matings in a predominantly selfing freshwater snail, Proceedings of the Royal Society of London. Series B: Biological Sciences 262, no.13641364 (Jan 1997): 119–125.https://doi.org/10.1098/rspb.1995.0185P. Jarne, T. Städler Population genetic structure and mating system evolution in freshwater pulmonates, Experientia 51, no.55 (May 1995): 482–497.https://doi.org/10.1007/BF02143200S. G. Johnson, C. M. Lively, S. J. Schrag Evolution and ecological correlates of uniparental reproduction in freshwater snails, Experientia 51, no.55 (May 1995): 498–509.https://doi.org/10.1007/BF02143201Lana Knoll, Naida Zucker Is sexual selection operating in the androdioecious clam shrimp,Eulimnadia texana (Crustacea: Conchostraca)?, Hydrobiologia 298, no.1-31-3 (Feb 1995): 67–72.https://doi.org/10.1007/BF00033800Lana Knoll, Naida Zucker Is sexual selection operating in the androdioecious clam shrimp, Eulimnadia texana (Crustacea: Conchostraca)?, (Jan 1995): 67–72.https://doi.org/10.1007/978-94-011-0291-9_4Claudie Doums, Bernard Delay, Philippe Jarne A PROBLEM WITH THE ESTIMATE OF SELF-FERTILIZATION DEPRESSION IN THE HERMAPHRODITE FRESHWATER SNAIL BULINUS TRUNCATUS : THE EFFECT OF GROUPING, Evolution 48, no.22 (May 2017): 498–504.https://doi.org/10.1111/j.1558-5646.1994.tb01327.xB. Streit, T. Städler, K. Kuhn, M. Loew, M. Brauer, B. Schierwater Molecular markers and evolutionary processes in hermaphrodite freshwater snails, (Jan 1994): 247–260.https://doi.org/10.1007/978-3-0348-7527-1_14S. J. Schrag, D. Rollinson Effects of Schistosoma haematobium infection on reproductive success and male outcrossing ability in the simultaneous hermaphrodite, Bulinus truncatus (Gastropoda: Planorbidae), Parasitology 108, no.11 (Apr 2009): 27–34.https://doi.org/10.1017/S0031182000078483Flobert Njiokou, Christian Bellec, Patrick Berrebi, Bernard Delay, Philippe Jarne Do self-fertilization and genetic drift promote a very low genetic variability in the allotetraploid Bulinus truncatus (Gastropoda: Planorbidae) populations?, Genetical Research 62, no.22 (Apr 2009): 89–100.https://doi.org/10.1017/S0016672300031682B. Baur, X. Chen, A. Baur Genital dimorphism in natural populations of the land snail Chondrina clienta and the influence of the environment on its expression, Journal of Zoology 231, no.22 (Mar 2009): 275–284.https://doi.org/10.1111/j.1469-7998.1993.tb01917.xPHILIPPE JARNE, MARC VIANEY-LIAUD, BERNARD DELAY Selfing and outcrossing in hermaphrodite freshwater gastropods (Basommatophora): where, when and why, Biological Journal of the Linnean Society 49, no.22 (Jan 2008): 99–125.https://doi.org/10.1111/j.1095-8312.1993.tb00893.x Reproductive development in the hermaphroditic freshwater snail Physa monitored with complementing albino lines, Proceedings of the Royal Society of London. Series B: Biological Sciences 252, no.13341334 (Jan 1997): 109–114.https://doi.org/10.1098/rspb.1993.0053 Genetic evidence for low outcrossing rates in polyploid freshwater snails (Ancylus fluviatilis), Proceedings of the Royal Society of London. Series B: Biological Sciences 251, no.13321332 (Jan 1997): 207–213.https://doi.org/10.1098/rspb.1993.0031Stephanie J. Schrag, Andrew F. Read TEMPERATURE DETERMINATION OF MALE OUTCROSSING ABILITY IN A SIMULTANEOUS HERMAPHRODITE, Evolution 46, no.66 (May 2017): 1698–1707.https://doi.org/10.1111/j.1558-5646.1992.tb01162.x

Referência(s)
Altmetric
PlumX