Vanderpoorten, Alain ; Université de Liège - ULiège > Département de Biologie, Ecologie et Evolution > Biologie de l'évolution et de la conservation - aCREA-Ulg
Patino, J.
Désamoré, A.
Laenen, B.
Gorski, P.
Papp, B.
Hola, E.
Korpelainen, H.
Hardy, O.J.
Language :
English
Title :
To what extent are bryophytes efficient dispersers?
Barbé, M., Fenton, N. J., & Bergeron, Y. (2016). So close and yet so far away: Long-distance dispersal events govern bryophyte metacommunity reassembly. Journal of Ecology, 104, 1707–1719. https://doi.org/10.1111/1365-2745.12637
Bystriakova, N., Ansell, S. W., Russell, S. J., Grundmann, M., Vogel, J. C., & Schneider, H. (2014). Present, past and future of the European rock fern Asplenium fontanum: Combining distribution modelling and population genetics to study the effect of climate change on geographic range and genetic diversity. Annals of Botany, 113, 453–465. https://doi.org/10.1093/aob/mct274
Dellicour, S., Kastally, C., Hardy, O. J., & Mardulyn, P. (2014). Comparing phylogeographic hypotheses by simulating DNA sequences under a spatially explicit model of coalescence. Molecular Biology and Evolution, 31, 3359–3372.
Fordham, D. A., Bertelsmeier, C., Brook, B. W., Early, R., Neto, D., Brown, S. C., … Araújo, M. B. (2018). How complex should models be? Comparing correlative and mechanistic range dynamics models. Global Change Biology, 24, 1357–1370. https://doi.org/10.1111/gcb.13935
Garcia, C., Klein, E. K., & Jordano, P. (2017). Dispersal processes driving plant movement: Challenges for understanding and predicting range shifts in a changing world. Journal of Ecology, 105, 1–5. https://doi.org/10.1111/1365-2745.12705
Hardy, O. J., & Vekemans, X. (1999). Isolation by distance in a continuous population: Reconciliation between spatial autocorrelation analysis and population genetics models. Heredity, 83, 145–154. https://doi.org/10.1046/j.1365-2540.1999.00558.x
Hardy, O. J., & Vekemans, X. (2002). SPAGeDi: A versatile computer program to analyze spatial genetic structure at the individual or population levels. Molecular Ecology Notes, 2, 618–620.
Heuertz, M., Vekemans, X., Hausman, J. F., Palada, M., & Hardy, O. J. (2003). Estimating seed vs. pollen dispersal from spatial genetic structure in the common ash. Molecular Ecology, 12, 2483–2495. https://doi.org/10.1046/j.1365-294X.2003.01923.x
Holá, E., Košnar, J., & Kučera, J. (2015). Comparison of genetic structure of epixylic liverwort Crossocalyx Hellerianus between central European and Fennoscandian populations. PLoS ONE, 10, e0133134. https://doi.org/10.1371/journal.pone.0133134
Hubbell, S. P. (2001). The unified neutral theory of biodiversity and biogeography. Princeton and Oxford: Princeton University Press.
Hunt, H. V., Ansell, S. W., Russell, S. J., Schneider, H., & Vogel, J. C. (2009). Genetic diversity and phylogeography in two diploid ferns, Asplenium fontanum subsp. fontanum and A. petrarchae subsp. bivalens, in the western Mediterranean. Molecular Ecology, 18, 4940–4954.
Imai, R., Tsuda, Y., Matsumoto, S., Ebihara, A., & Watano, Y. (2016). The relationship between mating system and genetic diversity in diploid sexual populations of Cyrtomium falcatum in Japan. PLoS ONE, 11, e0163683. https://doi.org/10.1371/journal.pone.0163683
Johansson, V., Lönnell, N., Rannik, Ü., Sundberg, S., & Hylander, K. (2016). Air humidity thresholds trigger active moss spore release to extend dispersal in space and time. Functional Ecology, 30, 1196–1204.
Johansson, V., Lönnell, N., Sundberg, S., & Hylander, K. (2014). Release thresholds for moss spores: The importance of turbulence and sporophyte length. Journal of Ecology, 102, 721–729. https://doi.org/10.1111/1365-2745.12245
Kang, M., Huang, H., Jiang, M., & Lowe, A. J. (2008). Understanding population structure and historical demography in a conservation context: Population genetics of an endangered fern. Diversity and Distributions, 14, 799–807. https://doi.org/10.1111/j.1472-4642.2008.00484.x
Koenig, W. D., Van Vuren, D., & Hooge, P. N. (1996). Detectability, philopatry, and the distribution of dispersal distances in vertebrates. Trends in Ecology and Evolution, 11, 514–517. https://doi.org/10.1016/S0169-5347(96)20074-6
Ledent, A., Désamoré, A., Laenen, B., Mardulyn, P., McDaniel, S. F., Zanatta, F., … Vanderpoorten, A. (2019). No borders during the post-glacial assembly of European bryophytes. Ecology Letters, 22, 973–986.
Loiselle, B. A., Sork, V. L., Nason, J., & Graham, C. (1995). Spatial genetic structure of a tropical understory shrub, Psychotria officinalis (Rubiaceae). American Journal of Botany, 82, 1420–1425.
Lönnell, N., Hylander, K., Jonsson, B. G., & Sundberg, S. (2012). The fate of the missing spores — Patterns of realized dispersal beyond the closest vicinity of a sporulating moss. PLoS ONE, 7, e41987. https://doi.org/10.1371/journal.pone.0041987
Lönnell, N., Jonsson, B. G., & Hylander, K. (2014). Production of diaspores at the landscape level regulates local colonization: An experiment with a spore dispersed moss. Ecography, 37, 591–598. https://doi.org/10.1111/j.1600-0587.2013.00530.x
Lönnell, N., Norros, V., Sundberg, S., Rannik, U., Johansson, V., Ovaskainen, O., & Hylander, K. (2015). Testing a mechanistic dispersal model against a dispersal experiment with a wind-dispersed moss. Oikos, 124, 1232–1240. https://doi.org/10.1111/oik.01886
Medina, N. G., & Estébanez, B. (2014). Does spore ultrastructure mirror different dispersal strategies in mosses? A study of seven Iberian Orthotrichum species. PLoS ONE, 9, e112867. https://doi.org/10.1371/journal.pone.0112867
Munoz, F., Beeravolu, C. R., Pelissier, R., & Couteron, P. (2013). Do spatially- implicit estimates of neutral migration comply with seed dispersal data in tropical forests? PLoS ONE, 8, e72497.
Patiño, J., Carine, M. A., Mardulyn, P., Devos, N., Mateo, R. G., González-Mancebo, J. M., … Vanderpoorten, A. (2015). Approximate Bayesian Computation reveals the crucial role of oceanic islands for the assembly of continental biodiversity. Systematic Biology, 64, 579–589.
Patiño, J., & Vanderpoorten, A. (2019). Bryophyte biogeography. Critical Reviews in Plant Sciences, 37, 175–209. https://doi.org/10.1080/07352689.2018.1482444
Snäll, T., Fogelqvist, J., Ribeiro, P. J., & Lascoux, M. (2004). Spatial genetic structure in two congeneric epiphytes with different dispersal strategies analysed by three different methods. Molecular Ecology, 13, 2109–2119. https://doi.org/10.1111/j.1365-294X.2004.02217.x
Sundberg, S. (2005). Larger capsules enhance short-range spore dispersal in Sphagnum, but what happens further away? Oikos, 108, 115–124.
Sundberg, S. (2013). Spore rain in relation to regional sources and beyond. Ecography, 36, 364–373. https://doi.org/10.1111/j.1600-0587.2012.07664.x
Sundberg, S., Hansson, J., & Rydin, H. (2006). Colonization of Sphagnum on land uplift islands in the Baltic Sea: Time, area, distance and life history. Journal of Biogeography, 33, 1479–1491. https://doi.org/10.1111/j.1365-2699.2006.01520.x
Szövényi, P., Sundberg, S., & Shaw, A. J. (2012). Long-distance dispersal and genetic structure of natural populations: An assessment of the inverse isolation hypothesis in peat mosses. Molecular Ecology, 21, 5461–5472. https://doi.org/10.1111/mec.12055
Thompson, P. M., & Goodman, S. (1997). Direct and indirect estimates of dispersal distances. Trends in Ecology and Evolution, 12, 195–196. https://doi.org/10.1016/S0169-5347(97)84095-5
Vekemans, X., & Hardy, O. J. (2004). New insights from fine-scale spatial genetic structure analyses in plant populations. Molecular Ecology, 13, 921–935. https://doi.org/10.1046/j.1365-294X.2004.02076.x
Wang, J., Vanderpoorten, A., Hagborg, A., Goffinet, B., Laenen, B., & Patiño, J. (2017). Evidence for a latitudinal diversity gradient in liverworts and hornworts. Journal of Biogeography, 44, 487–488. https://doi.org/10.1111/jbi.12909
Wang, Z. J., & Guan, K. Y. (2011). Genetic structure and phylogeography of a relict tree fern, Sphaeropteris brunoniana (Cyatheaceae) from China and Laos inferred from cpDNA sequence variations: Implications for conservation. Journal of Systematics and Evolution, 49, 72–79. https://doi.org/10.1111/j.1759-6831.2010.00108.x
Zanatta, F. A., Vanderpoorten, A., Hedenäs, L., Johansson, V., Patiño, J., Lönnell, N., & Hylander, K. (2018). Under which humidity conditions are moss spore released? A comparison between species with perfect and specialized peristomes. Ecology & Evolution, 8, 11484–11491.
Zurrell, D., Thuiller, W., Pagel, J., Cabral, J. S., Münkemüller, T., Gravel, D., … Zimmermann, N. E. (2016). Benchmarking novel approaches for modelling species range dynamics. Global Change Biology, 22, 2651–2664.
