Section: Evolutionary Biology
Topic: Evolution, Genetics/Genomics, Population biology

Connectivity and selfing drives population genetic structure in a patchy landscape: a comparative approach of four co-occurring freshwater snail species

10.24072/pcjournal.29 - Peer Community Journal, Volume 1 (2021), article no. e21.

Get full text PDF Peer reviewed and recommended by PCI

The distribution of neutral genetic variation in subdivided populations is driven by the interplay between genetic drift, migration, local extinction and colonization. The influence of environmental and demographic factors has also been increasingly examined in empirical studies, but generally focusing on a single species. An open question is whether these factors will similarly, or idiosyncratically, affect a guild of species occupying the same, though exhibiting different traits, mating systems and histories. We addressed it by comparing the population genetic structure of the four most common species of hermaphroditic freshwater snails in Guadeloupe (Lesser Antilles), which occupy a network of patchily distributed sites experiencing temporal variation in water availability. We analyzed microsatellite variability in 21 to 43 populations per species, and built predictions on how several environmental and demographic variables, quantified from a long-term annual survey, as well as species traits, may affect the distribution of genetic variation. These species displayed similarities, such as fairly high levels of variation, but with marked differences among sites, as well as strong genetic differentiation and limited isolation by distance, which can be explained by passive dispersal (strong role of site connectivity), extinction/colonization dynamics and variation in local population size. They also exhibit differences, largely due to the mating system with less genetic diversity and more genetic differentiation in the two selfing species when compared to the two outcrossing ones. These differences can also be attributed to interspecific interactions resulting from the ongoing invasion of Guadeloupe by one of the species studied, which affects the demography of other species, and, to a limited extent, to local environmental factors. Our comparative approach shows both differences and uniqueness in the way species occupy the same landscape, and provides a possible entry to interspecific interactions in community assembly.

Published online:
DOI: 10.24072/pcjournal.29
Type: Research article
Jarne, Philippe 1; Lozano del Campo, Ana 1; Lamy, Thomas 2, 3; Chapuis, Elodie 4; Dubart, Maxime 5; Segard, Adeline 6; Canard, Elsa 7; Pointier, Jean-Pierre 8; David, Patrice 1

1 CEFE, Univ Montpellier, CNRS, EPHE, IRD, Montpellier, France
2 MARBEC, Univ Montpellier-CNRS-Ifremer-IRD, Sète, France
3 Marine Science Institute, University of California, Santa Barbara, California, 93106, USA
4 MIVEGEC Univ Montpellier-CNRS-IRD, Montpellier, France
5 Evo-Eco-Paleo, Univ Lille-CNRS, Lille, France
6 INTERTRYP, Univ Montpellier-IRD-Cirad, Montpellier, France
7 IGEPP, INRA-Univ Rennes 1, Rennes, France
8 CRIOBE, CNRS-EPHE-PSL Research University-Univ Perpignan, Perpignan, France
License: CC-BY 4.0
Copyrights: The authors retain unrestricted copyrights and publishing rights
@article{10_24072_pcjournal_29,
     author = {Jarne, Philippe and Lozano del Campo, Ana and Lamy, Thomas and Chapuis, Elodie and Dubart, Maxime and Segard, Adeline and Canard, Elsa and Pointier, Jean-Pierre and David, Patrice},
     title = {Connectivity and selfing drives population genetic structure in a patchy landscape: a comparative approach of four co-occurring freshwater snail species},
     journal = {Peer Community Journal},
     eid = {e21},
     publisher = {Peer Community In},
     volume = {1},
     year = {2021},
     doi = {10.24072/pcjournal.29},
     url = {https://peercommunityjournal.org/articles/10.24072/pcjournal.29/}
}
TY  - JOUR
AU  - Jarne, Philippe
AU  - Lozano del Campo, Ana
AU  - Lamy, Thomas
AU  - Chapuis, Elodie
AU  - Dubart, Maxime
AU  - Segard, Adeline
AU  - Canard, Elsa
AU  - Pointier, Jean-Pierre
AU  - David, Patrice
TI  - Connectivity and selfing drives population genetic structure in a patchy landscape: a comparative approach of four co-occurring freshwater snail species
JO  - Peer Community Journal
PY  - 2021
VL  - 1
PB  - Peer Community In
UR  - https://peercommunityjournal.org/articles/10.24072/pcjournal.29/
DO  - 10.24072/pcjournal.29
ID  - 10_24072_pcjournal_29
ER  - 
%0 Journal Article
%A Jarne, Philippe
%A Lozano del Campo, Ana
%A Lamy, Thomas
%A Chapuis, Elodie
%A Dubart, Maxime
%A Segard, Adeline
%A Canard, Elsa
%A Pointier, Jean-Pierre
%A David, Patrice
%T Connectivity and selfing drives population genetic structure in a patchy landscape: a comparative approach of four co-occurring freshwater snail species
%J Peer Community Journal
%D 2021
%V 1
%I Peer Community In
%U https://peercommunityjournal.org/articles/10.24072/pcjournal.29/
%R 10.24072/pcjournal.29
%F 10_24072_pcjournal_29
Jarne, Philippe; Lozano del Campo, Ana; Lamy, Thomas; Chapuis, Elodie; Dubart, Maxime; Segard, Adeline; Canard, Elsa; Pointier, Jean-Pierre; David, Patrice. Connectivity and selfing drives population genetic structure in a patchy landscape: a comparative approach of four co-occurring freshwater snail species. Peer Community Journal, Volume 1 (2021), article  no. e21. doi : 10.24072/pcjournal.29. https://peercommunityjournal.org/articles/10.24072/pcjournal.29/

Peer reviewed and recommended by PCI : 10.24072/pci.evolbiol.100130

Conflict of interest of the recommender and peer reviewers:
The recommender in charge of the evaluation of the article and the reviewers declared that they have no conflict of interest (as defined in the code of conduct of PCI) with the authors or with the content of the article.

[1] Abu Awad, D.; Billiard, S. The double edged sword: The demographic consequences of the evolution of self-fertilization, Evolution, Volume 71 (2017) no. 5, pp. 1178-1190 | DOI

[2] Agrawal, A. A. Community genetics: new insights into community ecology by integrating population genetics, Ecology, Volume 84 (2003) no. 3, pp. 543-544 | DOI

[3] Akaike, H. A new look at the statistical model identification, IEEE Transactions on Automatic Control, Volume 19 (1974) no. 6, pp. 716-723 | DOI

[4] Balkenhol, N.; Cushman, S.; Storfer, A.; Waits, L. Landscape Genetics: Concepts, methods, applications, John Wiley & Sons, Ltd, Chichester, UK, 2015 | DOI

[5] Barton, N.; Whitlock, M. C. The Evolution of Metapopulations, Metapopulation Biology, Elsevier, 1997, pp. 183-210 | DOI

[6] Bassar, R. D.; Simon, T.; Roberts, W.; Travis, J.; Reznick, D. N. The evolution of coexistence: Reciprocal adaptation promotes the assembly of a simple community, Evolution, Volume 71 (2017) no. 2, pp. 373-385 | DOI

[7] Bell, G. Neutral Macroecology, Science, Volume 293 (2001) no. 5539, pp. 2413-2418 | DOI

[8] Bell, G. Selection, Oxford University Press, 2008 | DOI

[9] Bousset, L.; Henry, P.-Y.; Sourrouille, P.; Jarne, P. Population biology of the invasive freshwater snail Physa acuta approached through genetic markers, ecological characterization and demography, Molecular Ecology, Volume 13 (2004) no. 7, pp. 2023-2036 | DOI

[10] Bousset, L.; Pointier, J.-P.; David, P.; Jarne, P. Neither variation loss, nor change in selfing rate is associated with the worldwide invasion of Physa acuta from its native North America, Biological Invasions, Volume 16 (2014) no. 8, pp. 1769-1783 | DOI

[11] Burkhart, J. J.; Peterman, W. E.; Brocato, E. R.; Romine, K. M.; Willis, M. M. S.; Ousterhout, B. H.; Anderson, T. L.; Drake, D. L.; Rowland, F. E.; Semlitsch, R. D.; Eggert, L. S. The influence of breeding phenology on the genetic structure of four pond‐breeding salamanders, Ecology and Evolution, Volume 7 (2016) no. 13, pp. 4670-4681 | DOI

[12] Chapuis, E.; Lamy, T.; Pointier, J.-P.; Juillet, N.; Ségard, A.; Jarne, P.; David, P. Bioinvasion Triggers Rapid Evolution of Life Histories in Freshwater Snails, The American Naturalist, Volume 190 (2017) no. 5, pp. 694-706 | DOI

[13] Charbonnel, N.; Angers, B.; Rasatavonjizay, R.; Bremond, P.; Debain, C.; Jarne, P. The influence of mating system, demography, parasites and colonization on the population structure of Biomphalaria pfeifferi in Madagascar, Molecular Ecology, Volume 11 (2002) no. 11, pp. 2213-2228 | DOI

[14] Charlesworth, B.; Charlesworth, D. Elements of evolutionary genetics, Roberts & Company Publishers, 2010

[15] Charlesworth, D. Effects of inbreeding on the genetic diversity of populations, Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, Volume 358 (2003) no. 1434, pp. 1051-1070 | DOI

[16] David, P.; Pujol, B.; Viard, F.; Castella, V.; Goudet, J. Reliable selfing rate estimates from imperfect population genetic data, Molecular Ecology, Volume 16 (2007) no. 12, pp. 2474-2487 | DOI

[17] Davis, M. A. Invasion biology, Oxford University Press, Oxford, 2008

[18] Dlugosch, K. M.; Parker, I. M. Founding events in species invasions: genetic variation, adaptive evolution, and the role of multiple introductions, Molecular Ecology, Volume 17 (2008) no. 1, pp. 431-449 | DOI

[19] Dubart, M.; Pantel, J. H.; Pointier, J.; Jarne, P.; David, P. Modeling competition, niche, and coexistence between an invasive and a native species in a two‐species metapopulation, Ecology, Volume 100 (2019) | DOI

[20] Dubois, M.-P.; Nicot, A.; Jarne, P.; David, P. Characterization of 15 polymorphic microsatellite markers in the freshwater snailAplexa marmorata(Mollusca, Gastropoda), Molecular Ecology Resources, Volume 8 (2008) no. 5, pp. 1062-1064 | DOI

[21] Duggan, I. C. The freshwater aquarium trade as a vector for incidental invertebrate fauna, Biological Invasions, Volume 12 (2010) no. 11, pp. 3757-3770 | DOI

[22] Ebbs, E. T.; Loker, E. S.; Brant, S. V. Phylogeography and genetics of the globally invasive snail Physa acuta Draparnaud 1805, and its potential to serve as an intermediate host to larval digenetic trematodes, BMC Evolutionary Biology, Volume 18 (2018) no. 1 | DOI

[23] Escobar, J. S.; Nicot, A.; David, P. The Different Sources of Variation in Inbreeding Depression, Heterosis and Outbreeding Depression in a Metapopulation of Physa acuta, Genetics, Volume 180 (2008) no. 3, pp. 1593-1608 | DOI

[24] Escobar, J. S.; Auld, J. R.; Correa, A. C.; Alonso, J. M.; Bony, Y. K.; Coutellec, M.; Koene, J. M.; Pointier, J.; Jarne, P.; David, P. Patterns of mating‐system evolution in hermaphroditic animals: correlations among selfing rate, inbreeding depression, and the timing of reproduction, Evolution, Volume 65 (2011) no. 5, pp. 1233-1253 | DOI

[25] Estoup, A.; Ravigné, V.; Hufbauer, R.; Vitalis, R.; Gautier, M.; Facon, B. Is There a Genetic Paradox of Biological Invasion?, Annual Review of Ecology, Evolution, and Systematics, Volume 47 (2016) no. 1, pp. 51-72 | DOI

[26] Excoffier, L.; Ray, N. Surfing during population expansions promotes genetic revolutions and structuration, Trends in Ecology & Evolution, Volume 23 (2008) no. 7, pp. 347-351 | DOI

[27] Facon, B.; David, P. Metapopulation Dynamics and Biological Invasions: A Spatially Explicit Model Applied to a Freshwater Snail, The American Naturalist, Volume 168 (2006) no. 6, pp. 769-783 | DOI

[28] Figuerola, J.; Green, A. J. Dispersal of aquatic organisms by waterbirds: a review of past research and priorities for future studies, Freshwater Biology, Volume 47 (2002) no. 3, pp. 483-494 | DOI

[29] Foll, M.; Gaggiotti, O. Identifying the Environmental Factors That Determine the Genetic Structure of Populations, Genetics, Volume 174 (2006) no. 2, pp. 875-891 | DOI

[30] Fréville, H.; Choquet, R.; Pradel, R.; Cheptou, P.-O. Inferring seed bank from hidden Markov models: new insights into metapopulation dynamics in plants, Journal of Ecology, Volume 101 (2013) no. 6, pp. 1572-1580 | DOI

[31] Frichot, E.; Mathieu, F.; Trouillon, T.; Bouchard, G.; François, O. Fast and Efficient Estimation of Individual Ancestry Coefficients, Genetics, Volume 196 (2014) no. 4, pp. 973-983 | DOI

[32] Frichot, E.; François, O. LEA: An R package for landscape and ecological association studies, Methods in Ecology and Evolution, Volume 6 (2015) no. 8, pp. 925-929 | DOI

[33] Fronhofer, E. A.; Kubisch, A.; Hilker, F. M.; Hovestadt, T.; Poethke, H. J. Why are metapopulations so rare?, Ecology, Volume 93 (2012) no. 8, pp. 1967-1978 | DOI

[34] Goudet, J. FSTAT, a program to estimate and test gene diversities and fixation indices. http://www2.unil.ch/popgen/softwares/fstat.htm, 2001

[35] Haag, C. R.; Riek, M.; Hottinger, J. W.; Pajunen, V. I.; Ebert, D. Genetic Diversity and Genetic Differentiation in Daphnia Metapopulations With Subpopulations of Known Age, Genetics, Volume 170 (2005) no. 4, pp. 1809-1820 | DOI

[36] Hanski, I.; Gaggiotti, O. E. Ecology, genetics and evolution of metapopulations, Elsevier Academic Press, 2004

[37] Heino, J.; Melo, A. S.; Siqueira, T.; Soininen, J.; Valanko, S.; Bini, L. M. Metacommunity organisation, spatial extent and dispersal in aquatic systems: patterns, processes and prospects, Freshwater Biology, Volume 60 (2015) no. 5, pp. 845-869 | DOI

[38] Hendry, A. P. Eco-evolutionary Dynamics, Princeton University Press, Princeton, 2017 | DOI

[39] Hubbell, S. P. The unified neutral theory of biodiversity and biogeography, Princeton University Press, 2001

[40] Hughes, J. M.; Huey, J. A.; Schmidt, D. J. Is realised connectivity among populations of aquatic fauna predictable from potential connectivity?, Freshwater Biology, Volume 58 (2013) no. 5, pp. 951-966 | DOI

[41] Ingvarsson, P. A metapopulation perspective on genetic diversity and differentiation in partially self-fertilizing plants, Evolution, Volume 56 (2002) no. 12, pp. 2368-2373 | DOI

[42] Jarne, P. Mating system, bottlenecks and genetic polymorphism in hermaphroditic animals, Genetical Research, Volume 65 (1995) no. 3, pp. 193-207 | DOI

[43] Jarne, P.; David, P. Quantifying inbreeding in natural populations of hermaphroditic organisms, Heredity, Volume 100 (2008) no. 4, pp. 431-439 | DOI

[44] Jarne, P.; Delay, B. Population genetics of freshwater snails, Trends in Ecology & Evolution, Volume 6 (1991) no. 12, pp. 383-386 | DOI

[45] Kappes, H.; Haase, P. Slow, but steady: dispersal of freshwater molluscs, Aquatic Sciences, Volume 74 (2012) no. 1, pp. 1-14 | DOI

[46] Lamy, T.; Gimenez, O.; Pointier, J.-P.; Jarne, P.; David, P. Metapopulation Dynamics of Species with Cryptic Life Stages, The American Naturalist, Volume 181 (2013) no. 4, pp. 479-491 | DOI

[47] Lamy, T.; Jarne, P.; Laroche, F.; Pointier, J.-P.; Huth, G.; Segard, A.; David, P. Variation in habitat connectivity generates positive correlations between species and genetic diversity in a metacommunity, Molecular Ecology, Volume 22 (2013) no. 17, pp. 4445-4456 | DOI

[48] Lamy, T.; Laroche, F.; David, P.; Massol, F.; Jarne, P. The contribution of species-genetic diversity correlations to the understanding of community assembly rules, Oikos, Volume 126 (2017) no. 6, pp. 759-771 | DOI

[49] Lamy, T.; Pointier, J. P.; Jarne, P.; David, P. Testing metapopulation dynamics using genetic, demographic and ecological data, Molecular Ecology, Volume 21 (2012) no. 6, pp. 1394-1410 | DOI

[50] Levins, R. Some Demographic and Genetic Consequences of Environmental Heterogeneity for Biological Control, Bulletin of the Entomological Society of America, Volume 15 (1969) no. 3, pp. 237-240 | DOI

[51] Lewontin, R. C. The genetic basis of evolutionary change, Columbia University Press, 1974

[52] Lounnas, M.; Correa, A. C.; Vázquez, A. A.; Dia, A.; Escobar, J. S.; Nicot, A.; Arenas, J.; Ayaqui, R.; Dubois, M. P.; Gimenez, T.; Gutiérrez, A.; González-Ramírez, C.; Noya, O.; Prepelitchi, L.; Uribe, N.; Wisnivesky-Colli, C.; Yong, M.; David, P.; Loker, E. S.; Jarne, P.; Pointier, J. P.; Hurtrez-Boussès, S. Self-fertilization, long-distance flash invasion and biogeography shape the population structure ofPseudosuccinea columellaat the worldwide scale, Molecular Ecology, Volume 26 (2017) no. 3, pp. 887-903 | DOI

[53] Manel, S.; Holderegger, R. Ten years of landscape genetics, Trends in Ecology & Evolution, Volume 28 (2013) no. 10, pp. 614-621 | DOI

[54] Manier, M. K.; Arnold, S. J. Ecological correlates of population genetic structure: a comparative approach using a vertebrate metacommunity, Proceedings of the Royal Society B: Biological Sciences, Volume 273 (2006) no. 1604, pp. 3001-3009 | DOI

[55] Alice, M.; Nicolas, P. Dinucleotide microsatellite loci reveal a high selfing rate in the freshwater snail Physa acuta, Molecular Ecology, Volume 8 (1999) no. 6, pp. 1076-1078 | DOI

[56] Morgan, J. A phylogeny of planorbid snails, with implications for the evolution of Schistosoma parasites, Molecular Phylogenetics and Evolution, Volume 25 (2002) no. 3, pp. 477-488 | DOI

[57] Nei, M. Molecular Evolutionary Genetics, Columbia University Press, 1987 | DOI

[58] Nei, M.; Maruyama, T.; Chakraborty, R. The bottleneck effect and genetic variability in populations, Evolution, Volume 29 (1975) no. 1, pp. 1-10 | DOI

[59] Nicot, A.; Jarne, P.; David, P. Development of polymorphic microsatellite loci in the hermaphroditic freshwater snailsDrepanotrema surinamenseandDrepanotrema depressissimum, Molecular Ecology Resources, Volume 9 (2009) no. 3, pp. 897-902 | DOI

[60] Oksanen, J.; Blanchet, F. G.; Kindt, R.; Legendre, P.; Minchin, P. R.; O'Hara, R. B.; et al Vegan - Community ecology package: Ordination, diversity and dissimilarities, 2015 (https:/github.com/vegandevs/vegan)

[61] Ortego, J.; García-Navas, V.; Noguerales, V.; Cordero, P. J. Discordant patterns of genetic and phenotypic differentiation in five grasshopper species codistributed across a microreserve network, Molecular Ecology, Volume 24 (2015) no. 23, pp. 5796-5812 | DOI

[62] Otto, S. P. Selective Interference and the Evolution of Sex, Journal of Heredity, Volume 112 (2021) no. 1, pp. 9-18 | DOI

[63] Pannell, J. R. The Evolution and Maintenance of Androdioecy, Annual Review of Ecology and Systematics, Volume 33 (2002) no. 1, pp. 397-425 | DOI

[64] Pannell, J. R. Evolution of the mating system in colonizing plants, Molecular Ecology, Volume 24 (2015) no. 9, pp. 2018-2037 | DOI

[65] Pantel, J. H.; Lamy, T.; Dubart, M.; Pointier, J.-P.; Jarne, P.; David, P. Metapopulation dynamics of multiple species in a heterogeneous landscape, Ecological Monographs, Volume In Press

[66] Petit, R. J.; El Mousadik, A.; Pons, O. Identifying Populations for Conservation on the Basis of Genetic Markers, Conservation Biology, Volume 12 (1998) no. 4, pp. 844-855 | DOI

[67] Pointier, J.-P. Guide to the freshwater molluscs of the Lesser Antilles, Conchbooks, 2008

[68] Pointier, J.-P.; Combes, C. La saison sèche en Guadeloupe et ses conséquences sur la démographie des mollusques dans les biotopes a Biomphalaria glabrata (Say, 1818), vecteur de la bilharziose intestinale, Revue d'Ecologie (Terre et Vie), Volume 30 (1976)

[69] Pointier, J.; David, P. Biological control of Biomphalaria glabrata, the intermediate host of schistosomes, by Marisa cornuarietis in ponds of Guadeloupe: long-term impact on the local snail fauna and aquatic flora, Biological Control, Volume 29 (2004) no. 1, pp. 81-89 | DOI

[70] Pringle, R. M.; Kartzinel, T. R.; Palmer, T. M.; Thurman, T. J.; Fox-Dobbs, K.; Xu, C. C. Y.; Hutchinson, M. C.; Coverdale, T. C.; Daskin, J. H.; Evangelista, D. A.; Gotanda, K. M.; A. Man in ’t Veld, N.; Wegener, J. E.; Kolbe, J. J.; Schoener, T. W.; Spiller, D. A.; Losos, J. B.; Barrett, R. D. H. Predator-induced collapse of niche structure and species coexistence, Nature, Volume 570 (2019) no. 7759, pp. 58-64 | DOI

[71] Pritchard, J. K.; Stephens, M.; Donnelly, P. Inference of Population Structure Using Multilocus Genotype Data, Genetics, Volume 155 (2000) no. 2, pp. 945-959 | DOI

[72] R Development Core Team R: A language and environment for statistical computing. Vienna, Austria. http://www.r-project.org/, 2005

[73] Raymond, M.; Rousset, F. An exact test for population differentiation, Evolution, Volume 49 (1995) no. 6, pp. 1280-1283 | DOI

[74] Reid, B. N.; Mladenoff, D. J.; Peery, M. Z. Genetic effects of landscape, habitat preference and demography on three co‐occurring turtle species, Molecular Ecology, Volume 26 (2017) no. 3, pp. 781-798 | DOI

[75] Roman, J.; Darling, J. Paradox lost: genetic diversity and the success of aquatic invasions, Trends in Ecology & Evolution, Volume 22 (2007) no. 9, pp. 454-464 | DOI

[76] Rousset, F. Genetic Differentiation and Estimation of Gene Flow from F-Statistics Under Isolation by Distance, Genetics, Volume 145 (1997) no. 4, pp. 1219-1228 | DOI

[77] Rousset, F. genepop’007: a complete re-implementation of the genepop software for Windows and Linux, Molecular Ecology Resources, Volume 8 (2008) no. 1, pp. 103-106 | DOI

[78] Sourrouille, P.; Debain, C.; Jarne, P. Microsatellite variation in the freshwater snail Physa acuta, Molecular Ecology Notes, Volume 3 (2003) no. 1, pp. 21-23 | DOI

[79] Storfer, A.; Murphy, M. A.; Evans, J. S.; Goldberg, C. S.; Robinson, S.; Spear, S. F.; Dezzani, R.; Delmelle, E.; Vierling, L.; Waits, L. P. Putting the ‘landscape’ in landscape genetics, Heredity, Volume 98 (2007) no. 3, pp. 128-142 | DOI

[80] Strauss, S. Y.; Lau, J. A.; Carroll, S. P. Evolutionary responses of natives to introduced species: what do introductions tell us about natural communities?, Ecology Letters, Volume 9 (2006) no. 3, pp. 357-374 | DOI

[81] Stuart, Y. E.; Campbell, T. S.; Hohenlohe, P. A.; Reynolds, R. G.; Revell, L. J.; Losos, J. B. Rapid evolution of a native species following invasion by a congener, Science, Volume 346 (2014) no. 6208, pp. 463-466 | DOI

[82] Tian-Bi, Y.-N. T.; Konan, J.-N. K.; Sangaré, A.; Ortega-Abboud, E.; Utzinger, J.; N’Goran, E. K.; Jarne, P. Spatio-temporal population genetic structure, relative to demographic and ecological characteristics, in the freshwater snail Biomphalaria pfeifferi in Man, western Côte d’Ivoire, Genetica, Volume 147 (2019) no. 1, pp. 33-45 | DOI

[83] Van Leeuwen, C. H. A.; Huig, N.; Van Der Velde, G.; Van Alen, T. A.; Wagemaker, C. A. M.; Sherman, C. D. H.; Klaassen, M.; Figuerola, J. How did this snail get here? Several dispersal vectors inferred for an aquatic invasive species, Freshwater Biology, Volume 58 (2013) no. 1, pp. 88-99 | DOI

[84] Vellend, M. Conceptual Synthesis in Community Ecology, The Quarterly Review of Biology, Volume 85 (2010) no. 2, pp. 183-206 | DOI

[85] Vellend, M. The Theory of Ecological Communities (MPB-57), Princeton University Press, 2016 | DOI

[86] Vellend, M.; Geber, M. A. Connections between species diversity and genetic diversity, Ecology Letters, Volume 8 (2005) no. 7, pp. 767-781 | DOI

[87] Viard, F.; Justy, F.; Jarne, P. The influence of self-fertilization and population dynamics on the genetic structure of subdivided populations: a case study using microsatellite markers in the freshwater snailbulinus truncatus, Evolution, Volume 51 (1997) no. 5, pp. 1518-1528 | DOI

[88] Vinarski, M. V. The history of an invasion: phases of the explosive spread of the physid snail Physella acuta through Europe, Transcaucasia and Central Asia, Biological Invasions, Volume 19 (2017) no. 4, pp. 1299-1314 | DOI

[89] Wares, J. P.; Hughes, A. R.; Grosberg, R. K. Mechanisms that drive evolutionary change: insights from species introductions and invasions In: Sax DF, Stachowicz JJ, Gaines SD (Eds.), Species invasions: insights into ecology, evolution, and biogeography (2005), pp. 229-257

[90] Weir, B. S. Genetic data analysis II, Sinauer Associates, 1996

[91] Weir, B. S.; Cockerham, C. C. Estimating F-statistics for the analysis of population structure, Evolution, Volume 38 (1984) no. 6, pp. 1358-1370 | DOI

[92] Wethington, A. R.; Lydeard, C. A molecular phylogeny of Physidae (Gastropoda: Basommatophora) based on mitochondrial DNA sequences, Journal of Molluscan Studies, Volume 73 no. 3, pp. 241-257 | DOI

[93] Whitlock, M. C.; Barton, N. H. The Effective Size of a Subdivided Population, Genetics, Volume 146 (1997) no. 1, pp. 427-441 | DOI

Cited by Sources: