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Life on the edge: reproductive mode and rate of invasive Phragmites australis patch expansion

  • Phragmites Invasion
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Abstract

The dynamics of plant invasions from initial colonization through patch expansion are driven in part by mode of reproduction, i.e., sexual (seed) and asexual (clonal fragments and expansion) means. Expansion of existing patches—both rate and mode of spread into a matrix of varying conditions—is important for predicting potential invader impacts. In this study, we used fine-scale genetic assessments and remote sensing to describe both the rate and mode of expansion for 20 Phragmites australis patches in flooded and unflooded wetland units on the Great Salt Lake, UT. We found that the majority of Phragmites patch expansion occurred via clonal spread but we also documented instances of (potentially episodic) seedling recruitment. The mode of patch expansion, inferred from patch edge genet richness, was unrelated to flooding in the wetland unit in the preceding growing season. The rate of Phragmites patch expansion varied from 0.09 to 0.35 year−1 and was unrelated to the mode of spread. In six patches monitored across two years, monoclonal patches stayed monoclonal, whereas patches with higher genet richness had a marked increase in diversity in the second year. The findings of the present study suggest how this partially clonal species can exploit the benefits of both sexual (i.e., genetic recombination, widespread dispersal, colonization of new areas) and asexual reproduction (i.e., stability of established clones suited to local environmental conditions) to become one of the most successful wetland plant invaders. To control this species, both forms of reproduction need to be fully addressed through targeted management actions.

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References

  • Albert A, Brisson J, Belzile F, Turgeon J, Lavoie C (2015) Strategies for a successful plant invasion: the reproduction of Phragmites australis in northeastern North America. J Ecol 103:1529–1537

    CAS  Google Scholar 

  • Altartouri A, Nurminen L, Jolma A (2014) Modeling the role of the close-range effect and environmental variables in the occurrence and spread of Phragmites australis in four sites on the Finnish coast of the Gulf of Finland and the Archipelago Sea. Ecol Evol 4:987–1005

    PubMed  PubMed Central  Google Scholar 

  • Alvarez MG, Tron F, Mauchamp A (2005) Sexual versus asexual colonization by Phragmites australis: 25-year reed dynamics in a Mediterranean marsh, southern France. Wetlands 25:639–647

    Google Scholar 

  • Amsberry L, Baker MA, Ewanchuk PJ, Bertness MD (2000) Clonal integration and the expansion of Phragmites australis. Ecol Appl 10:1110–1118

    Google Scholar 

  • Armstrong J, Afreen-Zobayed F, Blyth S, Armstrong W (1999) Phragmites australis: effects of shoot submergence on seedling growth and survival and radial oxygen loss from roots. Aquat Bot 64:275–289

    Google Scholar 

  • Baldwin AH, Kettenring KM, Whigham DF (2010) Seed banks of Phragmites australis-dominated brackish wetlands: relationships to seed viability, inundation, and land cover. Aquat Bot 93:163–169

    Google Scholar 

  • Bart D, Burdick D, Chambers R, Hartman JM (2006) Human facilitation of Phragmites australis invasions in tidal marshes: a review and synthesis. Wetl Ecol Manag 14:53–65

    Google Scholar 

  • Belzile F, Labbé J, LeBlanc M-C, Lavoie C (2010) Seeds contribute strongly to the spread of the invasive genotype of the common reed (Phragmites australis). Biol Invasions 12:2243–2250

    Google Scholar 

  • Bhattarai GP, Cronin JT (2014) Hurricane activity and the large-scale pattern of spread of an invasive plant species. PLoS One 9:e98478

    PubMed  PubMed Central  Google Scholar 

  • Brisson J, de Blois S, Lavoie C (2010) Roadside as invasion pathway for common reed (Phragmites australis). Invasive Plant Sci Manag 3:506–514

    Google Scholar 

  • Chambers R, Osgood D, Bart D, Montalto F (2003) Phragmites australis invasion and expansion in tidal wetlands: interactions among salinity, sulfide, and hydrology. Estuaries 26:398–406

    CAS  Google Scholar 

  • Clevering OA, Lissner J (1999) Taxonomy, chromosome numbers, clonal diversity and population dynamics of Phragmites australis. Aquat Bot 64:185–208

    Google Scholar 

  • Congalton RG (1991) A review of assessing the accuracy of classifications of remotely sensed data. Remote Sens Environ 37:35–46

    Google Scholar 

  • Daehler CC (1998) Variation in self-fertility and the reproductive advantage of self-fertility for an invading plant (Spartina alterniflora). Evol Ecol 12:553–568

    Google Scholar 

  • Daehler CC, Strong DR (1994) Variable reproductive output among clones of Spartina alterniflora (Poaceae) invading San Francisco Bay, California: the influence of herbivory, pollination, and establishment site. Am J Bot 81:307–313

    Google Scholar 

  • Dong M, Lu B-R, Zhang H-B, Chen J-K, Li B (2006) Role of sexual reproduction in the spread of an invasive clonal plant Solidago canadensis revealed using intersimple sequence repeat markers. Plant Species Biol 21:13–18

    Google Scholar 

  • Dorken ME, Eckert CG (2001) Severely reduced sexual reproduction in northern populations of a clonal plant, Decodonverticillatus (Lythraceae). J Ecol 89:339–350

    Google Scholar 

  • Douhovnikoff V, Hazelton EL (2014) Clonal growth: invasion or stability? A comparative study of clonal architecture and diversity in native and introduced lineages of Phragmites australis (Poaceae). Am J Bot 101:1577–1584

    PubMed  Google Scholar 

  • Downard R, Endter-Wada J (2013) Keeping wetlands wet in the western United States: adaptations to drought in agriculture-dominated human-natural systems. J Environ Manag 131:394–406

    Google Scholar 

  • Downard R, Endter-Wada J, Kettenring K (2014) Adaptive wetland management in an uncertain and changing arid environment. Ecol Soc 19:23

    Google Scholar 

  • Eriksson O (1989) Seedling dynamics and life histories in clonal plants. Oikos 55:231–238

    Google Scholar 

  • Foody GM (2008) RVM-based multi-class classification of remotely sensed data. Int J Remote Sens 29:1817–1823

    Google Scholar 

  • Grace JB (1993) The adaptive significance of clonal reproduction in angiosperms: an aquatic perspective. Aquat Bot 44:159–180

    Google Scholar 

  • Grimsby JL, Tsirelson D, Gammon MA, Kesseli R (2007) Genetic diversity and clonal vs. sexual reproduction in Fallopia spp. (Polygonaceae). Am J Bot 94:957–964

    PubMed  Google Scholar 

  • Halkett F, Simon J-C, Balloux F (2005) Tackling the population genetics of clonal and partially clonal organisms. Trends Ecol Evol 20:194–201

    PubMed  Google Scholar 

  • Havens KJ, Berquist H, Priest WI (2003) Common reed grass, Phragmites australis, expansion into constructed wetlands: are we mortgaging our wetland future? Estuaries 26:417–422

    Google Scholar 

  • Hazelton EL, Mozdzer TJ, Burdick DM, Kettenring KM, Whigham DF (2014) Phragmites australis management in the United States: 40 years of methods and outcomes. AoB Plants 6:plu001

    PubMed  PubMed Central  Google Scholar 

  • Hazelton EL, McCormick MK, Sievers M, Kettenring KM, Whigham DF (2015) Stand age is associated with clonal diversity, but not vigor, community structure, or insect herbivory in Chesapeake Bay Phragmites australis. Wetlands 35:877–888

    Google Scholar 

  • Honnay O, Bossuyt B (2005) Prolonged clonal growth: escape route or route to extinction? Oikos 108:427–432

    Google Scholar 

  • Howard RJ, Turluck TD (2013) Phragmites australis expansion in a restored brackish marsh: documentation at different time scales. Wetlands 33:207–215

    Google Scholar 

  • Hudon C, Gagnon P, Jean M (2005) Hydrological factors controlling the spread of common reed (Phragmites australis) in the St. Lawrence River (Québec, Canada). Ecoscience 12:347–357

    Google Scholar 

  • Jensen JR (2005) Introductory digital image processing: A remote sensing perspective. Pearson Education Inc, Upper Saddle River

    Google Scholar 

  • Kettenring KM, Mock KE (2012) Genetic diversity, reproductive mode, and dispersal differ between the cryptic invader, Phragmites australis, and its native conspecific. Biol Invasions 14:2489–2504

    Google Scholar 

  • Kettenring KM, McCormick MK, Baron HM, Whigham DF (2010) Phragmites australis (common reed) invasion in the Rhode River subestuary of the Chesapeake Bay: disentangling the effects of foliar nutrients, genetic diversity, patch size, and seed viability. Estuar Coasts 33:118–126

    CAS  Google Scholar 

  • Kettenring KM, McCormick MK, Baron HM, Whigham DF (2011) Mechanisms of Phragmites australis invasion: feedbacks among genetic diversity, nutrients, and sexual reproduction. J Appl Ecol 48:1305–1313

    Google Scholar 

  • Kettenring KM, de Blois S, Hauber DP (2012) Moving from a regional to a continental perspective of Phragmites australis invasion in North America. AoB plants 2012:pls040

    PubMed  PubMed Central  Google Scholar 

  • Kettenring KM, Whigham DF, Hazelton EL, Gallagher SK, Weiner HM (2015) Biotic resistance, disturbance, and mode of colonization impact the invasion of a widespread, introduced wetland grass. Ecol Appl 25:466–480

    PubMed  Google Scholar 

  • Kirk H, Paul J, Straka J, Freeland JR (2011) Long-distance dispersal and high genetic diversity are implicated in the invasive spread of the common reed, Phragmites australis (Poaceae), in northeastern North America. Am J Bot 98:1180–1190

    PubMed  Google Scholar 

  • Koppitz H (1999) Analysis of genetic diversity among selected populations of Phragmites australis world-wide. Aquat Bot 64:209–221

    Google Scholar 

  • Koppitz H, Kühl H (2000) To the importance of genetic diversity of Phragmites australis in the development of reed stands. Wetl Ecol Manag 8:403–414

    Google Scholar 

  • Koppitz H, Kühl H, Hesse K, Kohl JG (1997) Some aspects of the importance of genetic diversity in Phragmites australis (Cav.) Trin. ex Steudel for the development of reed stands. Bot Acta 110:217–223

    Google Scholar 

  • Kulmatiski A, Beard KH, Meyerson LA, Gibson JR, Mock KE (2011) Nonnative Phragmites australis invasion into Utah wetlands. West N Am Nat 70:541–552

    Google Scholar 

  • Lathrop RG, Windham L, Montesano P (2003) Does Phragmites expansion alter the structure and function of marsh landscapes? Patterns and processes revisited. Estuaries 26:423–435

    Google Scholar 

  • Maheu-Giroux M, de Blois S (2007) Landscape ecology of Phragmites australis invasion in networks of linear wetlands. Landsc Ecol 22:285–301

    Google Scholar 

  • Mauchamp A, Blanch S, Grillas P (2001) Effects of submergence on the growth of Phragmites australis seedlings. Aquat Bot 69:147–164

    Google Scholar 

  • McCormick MK, Kettenring KM, Baron HM, Whigham DF (2010a) Extent and reproductive mechanisms of Phragmites australis spread in brackish wetlands in Chesapeake Bay, Maryland (USA). Wetlands 30:67–74

    Google Scholar 

  • McCormick MK, Kettenring KM, Baron HM, Whigham DF (2010b) Spread of invasive Phragmites australis in estuaries with differing degrees of development: genetic patterns, Allee effects and interpretation. J Ecol 98:1369–1378

    Google Scholar 

  • Meirmans PG, Van Tienderen PH (2004) GENOTYPE and GENODIVE: two programs for the analysis of genetic diversity of asexual organisms. Mol Ecol Notes 4:792–794

    Google Scholar 

  • Meyerson LA, Lambert AM, Saltonstall K (2010) A tale of three lineages: expansion of common reed (Phragmites australis) in the US Southwest and Gulf Coast. Invasive Plant Sci Manag 3:515–520

    Google Scholar 

  • Minchinton TE, Bertness MD (2003) Disturbance-mediated competition and the spread of Phragmites australis in a coastal marsh. Ecol Appl 13:1400–1416

    Google Scholar 

  • Mock KE, Brim-Box JC, Miller MP, Downing ME, Hoeh WR (2004) Genetic diversity and divergence among freshwater mussel (Anodonta) populations in the Bonneville Basin of Utah. Mol Ecol 13:1085–1098

    PubMed  CAS  Google Scholar 

  • Olson B, Lindsey K, Hirschboeck V (2004) Habitat management plan: Bear River Migratory Bird Refuge, Brigham City, Utah. US Department of the Interior Fish and Wildlife Service, Brigham City

    Google Scholar 

  • Pappert RA, Hamrick J, Donovan LA (2000) Genetic variation in Pueraria lobata (Fabaceae), an introduced, clonal, invasive plant of the southeastern United States. Am J Bot 87:1240–1245

    PubMed  CAS  Google Scholar 

  • Peakall R, Smouse PE (2006) GENALEX 6: genetic analysis in excel. Population genetic software for teaching and research. Mol Ecol Notes 6:288–295

    Google Scholar 

  • Peakall R, Smouse PE (2012) GenAlEx 6.5: genetic analysis in excel. Population genetic software for teaching and research—an update. Bioinformatics 28:2537–2539

    PubMed  PubMed Central  CAS  Google Scholar 

  • Philipp KR, Field RT (2005) Phragmites australis expansion in Delaware Bay salt marshes. Ecol Eng 25:275–291

    Google Scholar 

  • Rice D, Rooth J (2000) Colonization and expansion of Phragmites australis in upper Chesapeake Bay tidal marshes. Wetlands 20:280–299

    Google Scholar 

  • Saltonstall K (2002) Cryptic invasion by a non-native genotype of the common reed, Phragmites australis, into North America. Proc Natl Acad Sci 99:2445–2449

    PubMed  PubMed Central  CAS  Google Scholar 

  • Silvertown J (2008) The evolutionary maintenance of sexual reproduction: evidence from the ecological distribution of asexual reproduction in clonal plants. Int J Plant Sci 169:157–168

    Google Scholar 

  • ter Heerdt GN, Drost HJ (1994) Potential for the development of marsh vegetation from the seed bank after a drawdown. Biol Conserv 67:1–11

    Google Scholar 

  • Thayananthan A, Navaratnam R, Stenger B, Torr PH, Cipolla R (2006) Multivariate relevance vector machines for tracking. Springer, Berlin

    Google Scholar 

  • Tipping ME (2001) Sparse Bayesian learning and the relevance vector machine. J Mach Learn Research 1:211–244

    Google Scholar 

  • Vanderlinder MS, Neale CM, Rosenberg DE, Kettenring KM (2013) Use of remote sensing to assess changes in wetland plant communities over an 18-year period: a case study from the Bear River Migratory Bird Refuge, Great Salt Lake, Utah. West N Am Nat 74:33–46

    Google Scholar 

  • Viera AJ, Garrett JM (2005) Understanding interobserver agreement: the kappa statistic. Fam Med 37:360–363

    PubMed  Google Scholar 

  • Vos P, Hogers R, Bleeker M, Reijans M, Van de Lee T, Hornes M, Friters A, Pot J, Paleman J, Kuiper M (1995) AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414

    PubMed  PubMed Central  CAS  Google Scholar 

  • Warren RS, Fell PE, Grimsby JL, Buck EL, Rilling GC, Fertik RA (2001) Rates, patterns, and impacts of Phragmites australis expansion and effects of experimental Phragmites control on vegetation, macroinvertebrates, and fish within tidelands of the lower Connecticut River. Estuaries 24:90–107

    Google Scholar 

  • Weisner SE, Graneli W, Ekstam B (1993) Influence of submergence on growth of seedlings of Scirpus lacustris and Phragmites australis. Freshw Biol 29:371–375

    Google Scholar 

  • Welsh L, Endter-Wada J, Downard R, Kettenring K (2013) Developing adaptive capacity to droughts: the rationality of locality. Ecol Soc 18:7

    Google Scholar 

  • Wilcox DA (2012) Response of wetland vegetation to the post-1986 decrease in Lake St. Clair water levels: seed-bank emergence and beginnings of the Phragmites australis invasion. J Great Lakes Res 38:270–277

    Google Scholar 

  • Wilcox KL, Petrie SA, Maynard LA, Meyer SW (2003) Historical distribution and abundance of Phragmites australis at Long Point, Lake Erie, Ontario. J Great Lakes Res 29:664–680

    Google Scholar 

  • Wilson EO, Bossert WH (1971) A primer of population biology. Sinauer Associates, Sunderland

    Google Scholar 

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Acknowledgments

We thank Shannon Clemens Syrstad and Omar Alminagorta for assistance with the map production, and Rebekah Downard and Ben Crabb for their help with leaf collection. We also thank Dr. Austin Jensen and the crew of the AggieAir Flying Circus Service Center at the Utah Water Research Laboratory for their work in acquiring the high-resolution aerial imagery used in this research. Funding was provided by the U.S. Geological Survey (104(b) Program).

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Correspondence to Karin M. Kettenring.

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Guest Editors: Laura A. Meyerson and Kristin Saltonstall/ Phragmites invasion.

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Kettenring, K.M., Mock, K.E., Zaman, B. et al. Life on the edge: reproductive mode and rate of invasive Phragmites australis patch expansion. Biol Invasions 18, 2475–2495 (2016). https://doi.org/10.1007/s10530-016-1125-2

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