Abstract
Nonnative Phragmites is among the most invasive plants in the U.S. Atlantic coast tidal wetlands, whereas the native Phragmites has declined. Native and nonnative patches growing side by side provided an ideal setting for studying mechanisms that enable nonnative Phragmites to be a successful invader. We conducted an inventory followed by genetic analysis and compared differences in growth patterns and ventilation efficiency between adjacent native and nonnative Phragmites stands. Genetic analysis of 212 patches revealed that only 14 were native suggesting that very few native Phragmites populations existed in the study area. Shoot density decreased towards the periphery of native patches, but not in nonnative patches. Ventilation efficiency was 300 % higher per unit area for nonnative than native Phragmites, likely resulting in increased oxidation of the rhizosphere and invasive behavior of nonnative Phragmites. Management of nonnative Phragmites stands should include mechanisms that inhibit pressurized ventilation of shoots.
References
Anderson, D.R., W.A. Link, D.H. Johnson, and K.P. Burnham. 2001. Suggestions for presenting the results of data analyses. Journal of Wildlife Management 65: 373–378.
Armstrong, J., and W. Armstrong. 1991. A convective through-flow of gases in Phragmites australis (Cav.) Trin. ex Steud. Aquatic Botany 39: 75–88.
Baker, H.G. 1974. The evolution of weeds. Annual Review of Ecology and Systematics 5: 1–24.
Bart, D., and J.M. Hartman. 2000. Environmental determinants of Phragmites australis expansion in a New Jersey salt marsh: an experimental approach. Oikos 89: 59–69.
Bart, D., and J.M. Hartman. 2003. The role of large rhizome dispersal and low salinity windows in the establishment of common reed, Phragmites australis, in salt marshes: New links to human activities. Estuaries 26: 436–443.
Bertness, M.D., P.J. Ewanchuk, and B.R. Silliman. 2002. Anthropogenic modification of New England salt marsh landscapes. Proceedings of the National Academy of Sciences of the United States of America 99: 1395–1398.
Brix, H., B.K. Sorrell, and P.T. Orr. 1992. Internal pressurization and convective gas flow in some emergent freshwater macrophytes. Limnology and Oceanography 37: 1420–1433.
Burnham, K.P., and D.R. Anderson. 2002. Model selection and multimodel inference: A practical information-theoretic approach, 2nd ed. New York: Springer.
Chambers, R.M., L.A. Meyerson, and K. Saltonstall. 1999. Expansion of Phragmites australis into tidal wetlands of North America. Aquatic Botany 64: 261–273.
Chambers, R.M., T.J. Mozdzer, and J.C. Ambrose. 1998. Effects of salinity and sulfide on the distribution of Phragmites australis and Spartina alterniflora in a tidal saltmarsh. Aquatic Botany 62: 161–169.
Colmer, T.D. 2003. Long-distance transport of gases in plants: A perspective on internal aeration and radial oxygen loss from roots. Plant, Cell & Environment 26: 17–36.
Cronk, J.K., and M.S. Fennessy. 2001. Wetland plants: Biology and ecology. Boca Raton: Lewis Publishers.
Daehler, C.C., and D.R. Strong. 1996. Status, prediction and prevention of introduced cordgrass Spartina spp invasions in Pacific estuaries. USA Biological Conservation 78: 51–58.
Ehrenfeld, J.G. 2003. Effects of exotic plant invasions on soil nutrient cycling processes. Ecosystems 6: 503–523.
Eriksson, O. 1994. Stochastic population dynamics of clonal plants: Numerical experiments with ramet and genet models. Ecological Research 9: 257–268.
Grime, J.P. 1977. Evidence for the existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. The American Naturalist 111: 1169–1194.
Hartnett, D.C., and F.A. Bazzaz. 1985. The genet and ramet population dynamics of Solidago canadensis in an abandoned field. Journal of Ecology 73: 407.
Holdredge, C., M.D. Bertness, E. von Wettberg, and B.R. Silliman. 2010. Nutrient enrichment enhances hidden differences in phenotype to drive a cryptic plant invasion. Oikos 119: 1776–1784.
Johnston, C.A., D.M. Ghioca, M. Tulbure, B.L. Bedford, M. Bourdaghs, C.B. Frieswyk, L. Vaccaro, and J.B. Zedler. 2008. Partitioning vegetation response to anthropogenic stress to develop multi-taxa wetland indicators. Ecological Applications 18: 983–1001.
King, R.S., W.V. Deluca, D.F. Whigham, and P.P. Marra. 2007. Threshold effects of coastal urbanization on Phragmites australis (common reed) abundance and foliar nitrogen in Chesapeake Bay. Estuaries and Coasts 30: 469–481.
Lambertini, C., I.A. Mendelssohn, M.H.G. Gustafsson, B. Olesen, T. Riis, B.K. Sorrell, and H. Brix. 2012. Tracing the origin of Gulf Coast Phragmites (Poaceae): A story of long-distance dispersal and hybridization. American Journal of Botany 99: 538–551.
Lambrecht-McDowell, S.C., and S.R. Radosevich. 2005. Population demographics and trade-offs to reproduction of an invasive and noninvasive species of Rubus. Biological Invasions 7: 281–295.
League, M.T., E.P. Colbert, D.M. Seliskar, and J.L. Gallagher. 2006. Rhizome growth dynamics of native and exotic haplotypes of Phragmites australis (common reed). Estuaries and Coasts 29: 269–276.
Maheu-Giroux, M., and S. de Blois. 2007. Landscape ecology of Phragmites australis invasion in networks of linear wetlands. Landscape Ecology 22: 285–301.
Marks, M., B. Lapin, and J. Randall. 1994. Phragmites australis (Phragmites communis): Threats, management and monitoring. Natural Areas Journal 14: 285–294.
McCormick, M.K., K.M. Kettenring, H.M. Baron, and D.F. Whigham. 2010. Spread of invasive Phragmites australis in estuaries with differing degrees of development: Genetic patterns, Allee effects and interpretation. Journal of Ecology 98: 1369–1378.
McNabb, C.D., and T.R. Batterson. 1991. Occurrence of the common reed, Phragmites australis, along roadsides in Lower Michigan. Michigan Academician 23: 211–220.
Meadows, R.E., and 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.
Meyerson, L.A., K. Saltonstall, L. Windham, E. Kiviat, and S. Findlay. 2000. A comparison of Phragmites australis in freshwater and brackish marsh environments in North America. Wetlands Ecology and Management 8: 89–103.
Minchinton, T.E., and M.D. Bertness. 2003. Disturbance-mediated competition and the spread of Phragmites australis in a coastal marsh. Ecological Applications 13: 1400–1416.
Mozdzer, T.J., and J.C. Zieman. 2010. Ecophysiological differences between genetic lineages facilitate the invasion of non-native Phragmites australis in North American Atlantic coast wetlands. Journal of Ecology 98: 451–458.
Mozdzer, T.J., J.C. Zieman, and K.J. McGlathery. 2010. Nitrogen uptake by native and invasive temperate coastal macrophytes: Importance of dissolved organic nitrogen. Estuaries and Coasts 33: 784–797.
Niering, W.A., Warren, R.S., C.G. Weymouth. 1977. Our dynamic tidal marshes: Vegetation changes as revealed by peat analysis. Connecticut Arboretum Bulletin, 22.
Orson, R.A. 1999. A paleoecological assessment of Phragmites australis in New England tidal marshes: Changes in plant community structure during the last few millennia. Biological Invasions 1: 149–158.
Ostendorp, W. 1989. Dieback of reeds in Europe—A critical-review of literature. Aquatic Botany 35: 5–26.
Parker, I.M. 2000. Invasion dynamics of Cytisus scoparius: A matrix model approach. Ecological Applications 10: 726–743.
R Development Core Team. 2008. R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing.
Rice, D., J. Rooth, and J.C. Stevenson. 2000. Colonization and expansion of Phragmites australis in upper Chesapeake Bay tidal marshes. Wetlands 20: 280–299.
Rolletschek, H., T. Hartzendorf, A. Rolletschek, and J.G. Kohl. 1999. Biometric variation in Phragmites australis affecting convective ventilation and amino acid metabolism. Aquatic Botany 64: 291–302.
Rudrappa, T., J. Bonsall, and H.P. Bais. 2007. Root-secreted allelochemical in the noxious weed Phragmites australis deploys a reactive oxygen species response and microtubule assembly disruption to execute rhizotoxicity. Journal of Chemical Ecology 33: 1898–1918.
Sakai, A.K., F.W. Allendorf, J.S. Holt, D.M. Lodge, J. Molofsky, K.A. With, S. Baughman, R.J. Cabin, J.E. Cohen, N.C. Ellstrand, D.E. McCauley, P. O'Neil, I.M. Parker, J.N. Thompson, and S.G. Weller. 2001. The population biology of invasive species. Annual Review of Ecology and Systematics 32: 305–332.
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. 2003. A rapid method for identifying the origin of North American Phragmites populations using RFLP analysis. Wetlands 23: 1043–1047.
Saltonstall, K., P.M. Peterson, and R. Soreng. 2004. Recognition of Phragmites australis subsp. americanus (Poaceae: Arundinoideae) in North America: Evidence from morphological and genetic analyses. Sida 21: 683–692.
Seliskar, D.M., and J.L. Gallagher. 2000. Exploiting wild population diversity and somaclonal variation in the salt marsh grass Distichlis spicata (Poaceae) for marsh creation and restoration. American Journal of Botany 87: 141–146.
Seliskar, D.M., J.L. Gallagher, D.M. Burdick, and L.A. Mutz. 2002. The regulation of ecosystem functions by ecotypic variation in the dominant plant: A Spartina alterniflora salt-marsh case study. Journal of Ecology 90: 1–11.
Tucker, G.C. 1990. The genera of Arundinoidea (Gramineae) in the southeastern United States. Journal of the Arnold Arboretum 71: 14–171.
Tulbure, M.G. 2008. Invasion, environmental controls, and ecosystem feedbacks of Phragmites australis in coastal wetlands. South Dakota State University, p. 144.
Tulbure, M.G., and C.A. Johnston. 2010. Environmental conditions promoting non-native Phragmites australis expansion in Great Lakes Coastal Wetlands. Wetlands 30: 577–587.
Tulbure, M.G., C.A. Johnston, and D.L. Auger. 2007. Rapid invasion of a Great Lakes coastal wetland by non-native Phragmites australis and Typha. Journal of Great Lakes Research 33: 269–279.
van der Putten, W.H. 1997. Die-back of Phragmites australis in European wetlands: An overview of the European Research Programme on Reed Die-back and Progression (1993-1994). Aquatic Botany 59: 263–275.
Vasquez, E.A., E.P. Glenn, J.J. Brown, G.R. Guntenspergen, and 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.
Wijte, A., and J.L. Gallagher. 1996. Effect of oxygen availability and salinity on early life history stages of salt marsh plants. 1. Different germination strategies of Spartina alterniflora and Phragmites australis (Poaceaei). American Journal of Botany 83: 1337–1342.
Wikberg, S., and B.M. Svensson. 2003. Ramet demography in a ring-forming clonal sedge. Journal of Ecology 91: 847–854.
Acknowledgments
We thank Dr. Doug Samson from The Nature Conservancy for providing information about the King’s Creek Preserve, Drs. Joydeep Bhattacharjee and Neil Reese for help with choosing the instruments, Jay O’Neill for lab assistance, Dr. Kristin Saltonstall and Robert Meadows for suggestions regarding native stand locations in Maryland, Elaine Friebele for permission to sample Jug Bay wetlands, and Ned Gerber for allowing us to use his farm during the field season. Funding came through the Joseph F. Nelson scholarship to MGT. We thank the editors and two anonymous reviewers for helpful comments on an earlier draft.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Tulbure, M.G., Ghioca-Robrecht, D.M., Johnston, C.A. et al. Inventory and Ventilation Efficiency of Nonnative and Native Phragmites australis (Common Reed) in Tidal Wetlands of the Chesapeake Bay. Estuaries and Coasts 35, 1353–1359 (2012). https://doi.org/10.1007/s12237-012-9529-4
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12237-012-9529-4