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Potential for Spread of Algerian Sea Lavender (Limonium ramosissimum subsp. provinciale) in Tidal Marshes

Published online by Cambridge University Press:  20 January 2017

Gavin Archbald  and
Katharyn E. Boyer
Gavin Archbald*
Affiliation:
Romberg Tiburon Center for Environmental Studies and Department of Biology, San Francisco State University, 3152 Paradise Drive, Tiburon, CA 94920
Katharyn E. Boyer
Affiliation:
Romberg Tiburon Center for Environmental Studies and Department of Biology, San Francisco State University, 3152 Paradise Drive, Tiburon, CA 94920
*
Corresponding author's E-mail: [email protected]
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Abstract

We investigated the potential for an invasive sea lavender, Limonium ramosissimum subsp. provinciale (Algerian sea lavender; LIRA) to spread in San Francisco Estuary (SFE) tidal marshes by testing how two determinants of tidal marsh plant distribution, salinity and inundation, affect LIRA dispersal, germination, growth, and reproduction. Simulating dispersal in 0, 15, and 30 parts per thousand (ppt) salinity water, we found seeds remained afloat similarly regardless of salinity, and seed viability after floatation was high (88%); however, seeds in 0 ppt aquaria germinated after just 4 d, suggesting shorter dispersal distances in fresh than in brackish or saline water. Next, we compared LIRA and native halophyte seed germination in 0, 15, 30, and 45 ppt water. Percentage of germination was similar between species after 3 wk, but LIRA germinated faster in fresh water than all native species (90% vs. 5% germination after 4 d), suggesting a possible establishment advantage for LIRA at low salinities. Finally, we grew LIRA under crossed salinity and inundation levels in a tidal simulator for a growing season. LIRA growth and seed production increased when either salinity or inundation was reduced. We conclude that spread could be greatest among salt marshes due to high potential for seed dispersal in saline water, yet spread within marshes may be greatest in relatively lower salinity conditions where growth and reproduction are maximized.

Keywords

Algerian sea lavender, Limonium ramosissimum (Poir.) Maire subsp. provinciale (Pignatti) PignattiDispersalgerminationhalophyteinundationJaumealife history transitionspropagule pressureSalicorniasalinity gradienttransition zone
Type
Research Article
Information
Invasive Plant Science and Management , Volume 7 , Issue 3 , September 2014 , pp. 454 - 463
Copyright
Copyright © Weed Science Society of America 

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Footnotes

Current address of first author: Restoration Ecologist, H. T. Harvey & Associates, 983 University Avenue Building D, Los Gatos, CA 95032

References

Literature Cited

Archbald, G, Boyer, KE (2014) Distribution and invasion potential of Limonium ramosissimum subsp. provinciale in San Francisco Estuary salt marshes. San Francisco Estuary Watershed Sci 12(2): jmie_sfews_18824. http://escholarship.org/uc/item/61v8r7zw Google Scholar
Atwater, BF, Conard, SG, Dowden, JN, Hedel, CW, MacDonald, RL, Savage, W (1977) History, landforms, and vegetation of the Estuary's Tidal Marshes. San Francisco Pacific Division of the American Association for the Advancement of Science. 38 pGoogle Scholar
Atwater, BF, Hedel, CW (1976) Distribution of Seed Plants with Respect to Tide Levels and Water Salinity in the Natural Tidal Marshes of the Northern San Francisco Bay Estuary, CA. Menlo Park, CA U.S. Department of the Interior Geological Survey. Open File Report 76-389Google Scholar
Barbour, M, Keeler-Wolf, T, Schoenherr, AA (2007) Terrestrial Vegetation of California. 3rd edn. Berkeley University of California Press Google Scholar
Belote, RT, Jones, RH, Hood, SM, Wender, BW (2008) Diversity–invasibility across an experimental disturbance gradient in Appalachian forests. Ecology 89:183–192 Google Scholar
Bertness, MD, Shumway, W (1992) Salt tolerances and the distribution of fugitive salt marsh plants. Ecology 73:1842–1851 Google Scholar
Boorman, LA (1971) Studies in salt marsh ecology with special reference to the genus Limonium . J Ecol 59:103–120 Google Scholar
Callaway, JC, Josselyn, MN (1992) The introduction and spread of smooth cordgrass (Spartina alterniflora) in South San Francisco Bay. Estuaries 15:218–226 Google Scholar
Collins, JN (2002) Invasion of San Francisco Bay by Smooth Cordgrass, Spartina alterniflora: A Forecast of Geomorphic Effects on the Intertidal Zone. Oakland, CA Report prepared for US EPA Region 9. San Francisco Estuary Institute. 52 pGoogle Scholar
Collins, JN, Grossinger, RM (2004) Synthesis of Scientific Knowledge: For Maintaining and Improving Functioning of the South Bay Ecosystem and Restoring Tidal Salt Marsh and Associated Habitats over the Next 50 Years at Pond and Pond-Complex Scales. Oakland, CA San Francisco Estuary Institute. SFEI Report No: 308. 94 pGoogle Scholar
Consortium of California Herbaria (2012) Jepson Herbarium, University of California, Berkeley. http://ucjeps.berkeley.edu/consortium/. Accessed January 15, 2012Google Scholar
Crain, MC, Silliman, BR, Bertness, SL, Bertness, MD (2004) Physical and biotic drivers of plant distribution across estuarine salinity gradients. Ecology 85:2539–2549 Google Scholar
Davis, MA, Grime, JP, Thompson, K (2000) Fluctuating resources in plant communities: a general theory of invasibility. J Ecol 88:528–534 Google Scholar
Devillers-Terschuren, P, Devillers-Terschuren, J (2001) Convention of the Conservation of European Wildlife and Natural Habitats. Group of Experts for the setting up of the Emerald Network of Areas of Special Conservation Interest. Application and Development of the Palaearctic habitat classification in the Course of Setting Up the Emerald Project - Malta. Council of Europe, Strasbourg, France. 70 Google Scholar
Diggory, ZE, Parker, VT (2011) Seed supply and revegetation dynamics at restored tidal marshes, Napa River, CA. Restor Ecol 19(101):121–130 Google Scholar
Dytham, C (2012) Choosing and Using Statistics: A Biologist's Guide. 3rd edn. West Sussex, UK Wiley-Blackwell. 175 pGoogle Scholar
Elsey-Quirk, T, Middleton, BA, Proffitt, CE (2009) Seed floatation and germination of salt marsh plants: the effects of stratification, salinity, and/or inundation regime. Aquat Bot 91:40–46 Google Scholar
Eschtruth, AK, Battles, JJ (2009) Assessing the relative importance of disturbance, herbivory, diversity and propagule pressure in exotic plant invasion. Ecol Monog 79:265–280 Google Scholar
Flowers, JT, Colmer, TD (2008) Salinity tolerance in halophytes. New Phytol 179:945–963 Google Scholar
Grossinger, R, Alexander, J, Cohen, AN, Collins, JN (1998) Introduced Tidal Marsh Plants in the San Francisco Estuary: Regional Distribution and Priorities for Control. San Francisco Estuary Institute. Richmond, CA 55 pGoogle Scholar
Gul, B, Ansari, R, Flowers, T, Khan, MA (2013) Germination strategies of halophyte seeds under salinity. Environ Exp Bot 92:4–18 Google Scholar
Hinde, HP (1954) The vertical distribution of salt marsh phanerogams in relation to tide levels. Ecol Monogr 24:209–225 Google Scholar
Hobbes, RJ, Huenneke, LR (1992) Disturbance, diversity, and invasion: implications for conservation. Conserv Biol 6:324–337 Google Scholar
Holle, BV, Simberloff, D (2005) Ecological resistance to biological invasion overwhelmed by propagule pressure. Ecology 86:3212–3218 Google Scholar
Hubbard, DM, Page, HM (1997) Biology and Control of Invasive Sea Lavender, Limonium ramosissimum in Carpinteria Salt Marsh, California. San Buenaventura, CA U.S. Fish and Wildlife Service, Ventura Field Office. 36 pGoogle Scholar
Huiskes, AL, Koutstaal, BP, Herman, MJ, Beeftink, WG, Markusse, MM, DeMunck, W (1995) Seed dispersal of halophytes in tidal salt marshes. J Ecol 83:559–567 Google Scholar
Josselyn, M (1983) The Ecology of San Francisco Bay Tidal Marshes: A Community Profile. Washington, DC U.S. Fish and Wildlife Service, Division of Biological Services. FWS/OBS-83/23. 116 pGoogle Scholar
Khan, MA, Gul, B (2006) Halophyte seed germination. Pages 11–30 in Khan, MA, Weber, KJ, eds. Ecophysiology of High Salinity Tolerant Plants. Springer, Berlin. 20 pGoogle Scholar
Khan, MA, Weber, DJ (1986) Factors influencing seed germination in Salicornia pacifica var. utahensis . Am J Bot 73:1163–1167 Google Scholar
Kolar, CS, Lodge, DM (2001) Progress in invasion biology: predicting invaders. Trends Ecol Evol 16:199–204 Google Scholar
Leininger, SP, Foin, TC (2009) Lepidium latifolium reproductive potential and seed dispersal along salinity and moisture gradients. Biol Invasions 11:2351–2365 Google Scholar
Mahall, BE, Park, RB (1976) The ecotone between Spartina foliosa Trin. and Salicornia virginica L. in salt marshes of northern San Francisco Bay: II. Soil water and salinity. J Ecol 64:793–809 Google Scholar
Mitsch, WJ, Gosselink, JG (2000) Wetlands. 3rd edn. New York J Wiley. 920 pGoogle Scholar
Morgan, VH, Sytsma, MD (2013) Potential ocean dispersal of cordgrass (Spartina spp.) from core infestations. Invasive Plant Sci Manag 6:250–259 Google Scholar
Morzaria-Luna, H, Zedler, JB (2007) Does seed availability limit plant establishment during salt marsh restoration? Estuaries 30:12–25 Google Scholar
NOAA Tides and Currents. (2008) National Oceanographic and Atmospheric Administration, Center for Operational Oceanographic Products and Services http://www.tidesandcurrents.noaa.gov/noaatidepredictions/NOAATidesFacade.jsp?Stationid=9414449. Accessed January 5, 2008Google Scholar
Noe, GB, Zedler, JB (2001) Spatiotemporal heterogeneity of salt marsh seedling establishment in relation to the abiotic and biotic environment. J Veg Sci 12:61–74 Google Scholar
Pennings, SC, Callaway, RM (1992) Salt marsh plant zonation: the relative importance of competition and physical factors. Ecology 73:681–690 Google Scholar
Rand, TA (2000) Seed dispersal, habitat suitability and the distribution of halophytes across a salt marsh tidal gradient. J Ecol 88:608621 Google Scholar
Reynolds, LK, Boyer, KE (2010) Perennial pepperweed (Lepidium latifolium): properties of invaded tidal marshes. Invasive Plant Sci Manag 3:130–138 Google Scholar
Ryan, AB, Boyer, KE (2012) Nitrogen further promotes a dominant salt marsh plant in an increasingly saline environment. J Plant Ecol 5:429–441 Google Scholar
Schile, LM, Callaway, JC, Parker, VT, Vasey, MC (2011) Salinity and inundation influence productivity of the halophytic plant Sarcocornia pacifica . Wetlands 31:1165–1174 Google Scholar
Seliskar, DM (1985) Morphometric variations of five tidal marsh halophytes along environmental gradients. Am J Bot 72:1340–1352 Google Scholar
[SFEI] San Francisco Estuary Institute (2011) California Wetlands Portal http://www.sfei.org/wetlandtracker.org. Accessed March 4, 2011Google Scholar
Simberloff, D (2009) The role of propagule pressure in biological invasions. Annu Rev Ecol EvolSyst 40:81–102 Google Scholar
Spenst, RO (2006) The Biology and Ecology of Lepidium latifolium L. in the San Francisco Estuary and Their Implications for Eradication of this Invasive Weed. Ph.D Dissertation. Davis, CA University of California Davis. 96 pGoogle Scholar
Ungar, IA (1991) Ecophysiology of Vascular Halophytes. Boca Raton, FL CRC. 209 pGoogle Scholar
Ungar, IA (1995) Seed germination and seed-bank ecology of halophytes. In: Kigel, J, Galili, G, eds. Seed Development and Germination. New York Marcel and Dekker. 853 pGoogle Scholar
Watson, EB, Byrne, R (2009) Abundance and diversity of tidal marsh plants along the salinity gradient of the San Francisco Estuary: implications for global climate change. Plant Ecol 205:113–128 Google Scholar
Zedler, JB, Kercher, S (2004) Causes and consequences of invasive plants in wetlands: opportunities, opportunists, and outcomes. Crit Rev Plant Sci 23:431–452 Google Scholar