Abstract
In the Mississippi River Delta, the common wetland grass, Phragmites australis, displays high genetic diversity, as several genetically distinct populations are co-occurring. Differences in salinity tolerance may be an important factor determining these populations’ distribution in the delta. Our study investigated the salt tolerance of four genotypes exposed to 0, 10, 20, 30, and 40 ppt salinity. The growth rate, biomass, and the light-saturated photosynthetic rate were stimulated at 10 ppt salinity and inhibited at salinities higher than 20 ppt, compared to controls. Increased concentrations of Cl− and Na+ were found in the roots and older leaves of plants exposed to high salinities. Salt tolerance levels differed between genotypes. High salinity tolerance was mainly achieved by reduced water uptake and vacuole compartmentalization of toxic ions. The most tolerant genotype sustained biomass and photosynthesis even at 40 ppt, whereas the most sensitive genotype did not survive salinities higher than 20 ppt. Our findings show that the observed occurrence of different genotypes in the Mississippi River Delta is correlated to genetically determined differences in salinity tolerance. Further investigations are needed to better understand the role that salinity tolerance plays in the invasion of certain introduced P. australis genotypes.
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References
Achenbach, L., C. Lambertini & H. Brix, 2012. Phenotypic traits of Phragmites australis clones are not related to ploidy level and distribution range. AoB Plants. doi:10.1093/aobpla/pls017.
Achenbach, L., F. Eller, L. Nguyen & H. Brix, 2013. Differences in salinity tolerance of genetically distinct Phragmites australis clones. AoB Plants. doi:10.1093/aobpla/plt019.
Bazihizina, N., E. G. Barrett-Lennard & T. D. Colmer, 2012. Plant growth and physiology under heterogeneous salinity. Plant and Soil 354: 1–19.
Brix, H., 1999. Genetic diversity, ecophysiology and growth dynamics of reed (Phragmites australis)—introduction. Aquatic Botany 64: 179–184.
Bruton, M. N. & K. H. Cooper, 1980. Studies on the Ecology of Maputaland. Rhodes University, Grahamstown & Natal Branch of the Wildlife Society of South Africa, Durban.
Chambers, R. M., L. A. Meyerson & K. Saltonstall, 1999. Expansion of Phragmites australis into tidal wetlands of North America. Aquatic Botany 64: 261–273.
Clevering, O. A. & J. Lissner, 1999. Taxonomy, chromosome numbers, clonal diversity and population dynamics of Phragmites australis. Aquatic Botany 64: 185–208.
Den, H. C., J. Kvet & H. Sukopp, 1989. Reed: a common species in decline. Aquatic Botany 35: 1–4.
Fediuc, E., S. H. Lips & L. Erdei, 2005. O-Acetylserine (thiol) lyase activity in Phragmites and Typha plants under cadmium and NaCl stress conditions and the involvement of ABA in the stress response. Journal of Plant Physiology 162: 865–872.
Gao, L., S. Tang, L. Zhuge, M. Nie, Z. Zhu, B. Li & J. Yang, 2012. Spatial genetic structure in natural populations of Phragmites australis in a mosaic of saline habitats in the Yellow River Delta, China. Plos One 7: e43334.
Gorai, M., M. Ennajeh, H. Khemira & M. Neffati, 2010. Combined effect of NaCl-salinity and hypoxia on growth, photosynthesis, water relations and solute accumulation in Phragmites australis plants. Flora 205: 462–470.
Gorai, M., M. Ennajeh, H. Khemira & M. Neffati, 2011. Influence of NaCl-salinity on growth, photosynthesis, water relations and solute accumulation in Phragmites australis. Acta Physiologiae Plantarum 33: 963–971.
Hanganu, J., G. Mihail & H. Coops, 1999. Responses of ecotypes of Phragmites australis to increased seawater influence: a field study in the Danube Delta, Romania. Aquatic Botany 64: 351–358.
Hansen, D. L., C. Lambertini, A. Jampeetong & H. Brix, 2007. Clone-specific differences in Phragmites australis: effects of ploidy level and geographic origin. Aquatic Botany 86: 269–279.
Hauber, D. P., K. Saltonstall, D. A. White & C. S. Hood, 2011. Genetic variation in the common reed, Phragmites australis, in the Mississippi River Delta marshes: evidence for multiple introductions. Estuaries and Coasts 34: 851–862.
Hirtreiter, J. & D. Potts, 2012. Canopy structure, photosynthetic capacity and nitrogen distribution in adjacent mixed and monospecific stands of Phragmites australis and Typha latifolia. Plant Ecology 213: 821–829.
Hughes, H. & J. Hughes, 1992. A Directory of African Wetlands. IUCN, Gland; UNEP, Nairobi; WCMC, Cambridge.
Lambertini, C., M. H. G. Gustafsson, J. Frydenberg, J. Lissner, M. Speranza & H. Brix, 2006. A phylogeographic study of the cosmopolitan genus Phragmites (Poaceae) based on AFLPs. Plant Systematics and Evolution 258: 161–182.
Lambertini, C., M. H. G. Gustafsson, J. Frydenberg, M. Speranza & H. Brix, 2008. Genetic diversity patterns in Phragmites australis at the population, regional and continental scales. Aquatic Botany 88: 160–170.
Lambertini, C., I. A. Mendelssohn, M. H. G. Gustafsson, B. Olesen, T. Riis, B. K. Sorrell & H. Brix, 2012a. Tracing the origin of Gulf Coast Phragmites (Poaceae): a story of long-distance dispersal and hybridization. American Journal of Botany 99: 538–551.
Lambertini,C., F. Eller, L. Achenbach, L. Nguyen, W. Guo & H. Brix, 2012b. Revisiting Phragmites australis variation in the Danube Delta with DNA molecular techniques. Water Resources and Wetlands, Tulcea: 142–149.
Lessmann, J. M., H. Brix, V. Bauer, O. A. Clevering & F. A. Comin, 2001. Effect of climatic gradients on the photosynthetic responses of four Phragmites australis populations. Aquatic Botany 69: 109–126.
Lissner, J. & H. H. Schierup, 1997. Effects of salinity on the growth of Phragmites australis. Aquatic Botany 55: 247–260.
Lissner, J., H. H. Schierup, F. A. Comin & V. Astorga, 1997. Effects of climate on the salt tolerance of the common reed (Phragmites australis). Plant Physiology 114: 524.
Lissner, J., H. H. Schierup, F. A. Comin & V. Astorga, 1999. Effect of climate on the salt tolerance of two Phragmites australis populations. I. Growth, inorganic solutes, nitrogen relations and osmoregulation. Aquatic Botany 64: 317–333.
Matsushita, N. & T. Matoh, 1991. Characterization of Na+ exclusion mechanisms of salt-tolerant reed plants in comparison with salt-sensitive rice plants. Physiologia Plantarum 83: 170–176.
Meadows, R. E. & K. Saltonstall, 2007. Distribution of native and introduced Phragmites australis in freshwater and oligohaline tidal marshes of the Delmarva Peninsula and southern New Jersey. Journal of the Torrey Botanical Society 134: 99–107.
Munns, R. & M. Tester, 2008. Mechanisms of salinity tolerance. Annual Review of Plant Biology 59: 651–681.
Pagter, M., C. Bragato & H. Brix, 2005. Tolerance and physiological responses of Phragmites australis to water deficit. Aquatic Botany 81: 285–299.
Pagter, M., C. Bragato, M. Malagoli & H. Brix, 2009. Osmotic and ionic effects of NaCl and Na2SO4 salinity on Phragmites australis. Aquatic Botany 90: 43–51.
Parida, A. K. & A. B. Das, 2005. Salt tolerance and salinity effects on plants: a review. Ecotoxicology and Environmental Safety 60: 324–349.
Pauca-Comanescu, M., O. A. Clevering, J. Hanganu & M. Gridin, 1999. Phenotypic differences among ploidy levels of Phragmites australis growing in Romania. Aquatic Botany 64: 223–234.
Saltonstall, K., 2002. Cryptic invasion by a non-native genotype of the common reed, Phragmites australis, into North America. Proceedings of the National Academy of Sciences of the United States of America 99: 2445–2449.
Saltonstall, K., P. M. Peterson & R. J. Soreng, 2004. Recognition of Phragmites australis subsp Americanus (Poaceae: Arundinoideae) in North America: evidence from morphological and genetic analyses. SIDA Contributions to Botany 21: 683–692.
Vasquez, E. A., E. P. Glenn, J. J. Brown, G. R. Guntenspergen & S. G. Nelson, 2005. Salt tolerance underlies the cryptic invasion of North American salt marshes by an introduced haplotype of the common reed Phragmites australis (Poaceae). Marine Ecology-Progress Series 298: 1–8.
Vasquez, E. A., E. P. Glenn, G. R. Guntenspergen, J. J. Brown & S. G. Nelson, 2006. Salt tolerance and osmotic adjustment of Spartina alterniflora (Poaceae) and the invasive M haplotype of Phragmites australis (Poaceae) along a salinity gradient. American Journal of Botany 93: 1784–1790.
Acknowledgments
We thank Dr. Carla Lambertini for her essential guidance in choosing the clones and for her valuable comments on phylogeny and genotypic traits. Prof. Irving A. Mendelssohn and Shuwen Li from Louisiana State University, Prof. David A. White, Donald P. Hauber and Craig S. Hood from Loyola University are thanked for introducing us to the GC Delta and for help with the collection of the plant material. This work was funded by The Danish Council for Independent Research, Natural Sciences, via a grant to H.B. Additional travel and salary support was provided by the John P. Laborde Endowed Chair for Sea Grant Research and Technology Transfer Program. The Carlsberg Foundation funded the Li-Cor 6400XT equipment.
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Guest editors: M. T. Ferreira, M. O’Hare, K. Szoszkiewicz & S. Hellsten / Plants in Hydrosystems: From Functional Ecology to Weed Research
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Achenbach, L., Brix, H. Can differences in salinity tolerance explain the distribution of four genetically distinct lineages of Phragmites australis in the Mississippi River Delta?. Hydrobiologia 737, 5–23 (2014). https://doi.org/10.1007/s10750-013-1601-y
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DOI: https://doi.org/10.1007/s10750-013-1601-y