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Estuaries and Coasts

, Volume 42, Issue 8, pp 1991–2003 | Cite as

Climatic Controls on the Distribution of Foundation Plant Species in Coastal Wetlands of the Conterminous United States: Knowledge Gaps and Emerging Research Needs

  • Michael J. OslandEmail author
  • James B. Grace
  • Glenn R. Guntenspergen
  • Karen M. Thorne
  • Joel A. Carr
  • Laura C. Feher
Perspectives

Abstract

Foundation plant species play a critical role in coastal wetlands, often modifying abiotic conditions that are too stressful for most organisms and providing the primary habitat features that support entire ecological communities. Here, we consider the influence of climatic drivers on the distribution of foundation plant species within coastal wetlands of the conterminous USA. Using region-level syntheses, we identified 24 dominant foundation plant species within 12 biogeographic regions, and we categorized species and biogeographic regions into four groups: graminoids, mangroves, succulents, and unvegetated. Literature searches were used to characterize the level of research directed at each of the 24 species. Most coastal wetlands research has been focused on a subset of foundation species, with about 45% of publications directed at just one grass species—Spartina alterniflora. An additional 14 and 8% have been directed, respectively, at two mangrove species—Rhizophora mangle and Avicennia germinans. At the national scale, winter temperature extremes govern the distribution of mangrove forests relative to salt marsh graminoids, and arid conditions can produce hypersaline conditions that increase the dominance of succulent plants, algal mats, and unvegetated tidal flats (i.e., salt flats, salt pans) relative to graminoid and mangrove plants. Collectively, our analyses illustrate the diversity of foundation plant species in the conterminous USA and begin to elucidate the influence of climatic drivers on their distribution. However, our results also highlight critical knowledge gaps and identify emerging research needs for assessing climate change impacts. Given the importance of plant-mediated processes in coastal wetland ecosystems, there is a pressing need in many biogeographic regions for additional species- and functional group-specific research that can be used to better anticipate coastal wetland responses to rising sea levels and changing temperature and precipitation regimes.

Keywords

Coastal wetland Foundation species Plant functional group Salt marsh Mangrove forest United States 

Notes

Funding Information

This research was partially supported by the USGS Land Change Science Climate R&D Program, USGS Ecosystems Mission Area, Department of Interior Southeast Climate Adaptation Science Center, Department of Interior South Central Climate Adaptation Science Center, and the USGS Greater Everglades Priority Ecosystems Science Program. Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government.

Supplementary material

12237_2019_640_MOESM1_ESM.docx (204 kb)
ESM 1 (DOCX 203 kb)

References

  1. Alber, M. 2002. A conceptual model of estuarine freshwater inflow management. Estuaries 25 (6): 1246–1261.Google Scholar
  2. Alexander, H.D., and K.H. Dunton. 2002. Freshwater inundation effects on emergent vegetation of a hypersaline salt marsh. Estuaries and Coasts 25 (6): 1426–1435.Google Scholar
  3. Archibold, O.W. 2012. Ecology of world vegetation. Dordrecht, Netherlands: Springer Science & Business Media.Google Scholar
  4. Baldwin, A.H., P.J. Kangas, J.P. Megonigal, M.C. Perry, and D.F. Whigham. 2012. Coastal wetlands of Chesapeake Bay. In Wetland habitats of North America: ecology and conservation concerns, ed. D.P. Batzer and A.H. Baldwin. Berkeley, CA: University of California Press.Google Scholar
  5. Barbier, E.B., S.D. Hacker, C. Kennedy, E.W. Koch, A.C. Stier, and B.R. Silliman. 2011. The value of estuarine and coastal ecosystem services. Ecological Monographs 81 (2): 169–193.Google Scholar
  6. Battaglia, L.L., M.S. Woodrey, M.S. Peterson, K.S. Dillon, and J.M. Visser. 2012. Wetlands of the northern Gulf Coast. In Wetland habitats of North America: ecology and conservation concerns, ed. D.P. Batzer and A.H. Baldwin, 75–88. Berkeley, CA: University of California Press.Google Scholar
  7. Bertness, M.D., and R. Callaway. 1994. Positive interactions in communities. Trends in Ecology and Evolution 9 (5): 191–193.Google Scholar
  8. Bertness, M.D., and A.M. Ellison. 1987. Determinants of pattern in a New England salt marsh plant community. Ecological Monographs 57 (2): 129–147.Google Scholar
  9. Bruno, J.F., and M.D. Bertness. 2001. Habitat modification and facilitation in benthic marine communities. In Marine community ecology, ed. M.D. Bertness, S.D. Gaines, and M.E. Hay, 201–218. Sunderland, MA: Sinauer Associates.Google Scholar
  10. Bruno, J.F., J.J. Stachowicz, and M.D. Bertness. 2003. Inclusion of facilitation into ecological theory. Trends in Ecology & Evolution 18 (3): 119–125.Google Scholar
  11. Callaway, J.C., A.B. Borde, H.L. Diefenderfer, V.T. Parker, J.M. Rybczyk, and R.M. Thom. 2012. Pacific Coast tidal wetlands. In Wetland habitats of North America: ecology and conservation concerns, ed. D.P. Batzer and A.H. Baldwin, 103–116. Berkeley, CA: University of California Press.Google Scholar
  12. Cavanaugh, K.C., J.R. Kellner, A.J. Forde, D.S. Gruner, J.D. Parker, W. Rodriguez, and I.C. Feller. 2014. Poleward expansion of mangroves is a threshold response to decreased frequency of extreme cold events. Proceedings of the National Academy of Sciences 111 (2): 723–727.Google Scholar
  13. Cavanaugh, K.C., M.J. Osland, R. Bardou, G. Hinijosa-Arango, J.M. López-Vivas, J.D. Parker, and A.S. Rovai. 2018. Sensitivity of mangrove range limits to climate variability. Global Ecology and Biogeography 27 (8): 925–935.Google Scholar
  14. Cavanaugh, K.C., E.M. Dangremond, C.L. Doughty, A.P. Williams, J.D. Parker, M.A. Hayes, W. Rodriguez, and I.C. Feller. 2019. Climate-driven regime shifts in a mangrove–salt marsh ecotone over the past 250 years. Proceedings of the National Academy of Sciences.  https://doi.org/10.1073/pnas.1902181116.
  15. Cherry, J.A., K.L. McKee, and J.B. Grace. 2009. Elevated CO2 enhances biological contributions to elevation change in coastal wetlands by offsetting stressors associated with sea-level rise. Journal of Ecology 97 (1): 67–77.Google Scholar
  16. Conner, W.H., T.W. Doyle, and K.W. Krauss. 2007. Ecology of tidal freshwater forested wetlands of the southeastern United States. Dordrecht: Springer.Google Scholar
  17. Costanza, R., R. de Groot, P. Sutton, S. van der Ploeg, S.J. Anderson, I. Kubiszewski, S. Farber, and R.K. Turner. 2014. Changes in the global value of ecosystem services. Global Environmental Change 26: 152–158.Google Scholar
  18. Daly, C., M. Halbleib, J.I. Smith, W.P. Gibson, M.K. Doggett, G.H. Taylor, J. Curtis, and P.P. Pasteris. 2008. Physiographically sensitive mapping of climatological temperature and precipitation across the conterminous United States. International Journal of Climatology 28 (15): 2031–2064.Google Scholar
  19. Dame, R., M. Alber, D. Allen, M. Mallin, C. Montague, A. Lewitus, A. Chalmers, R. Gardner, C. Gilman, B. Kjerfve, J. Picnckney, and N. Smith. 2000. Estuaries of the south Atlantic coast of North America: their geographical signatures. Estuaries 23 (6): 793–819.Google Scholar
  20. Dayton, P.K. 1972. Toward an understanding of community resilience and the potential effects of enrichments to the benthos at McMurdo Sound, Antarctica. In Proceedings of the Colloquium on Conservation Problems in Antarctica, ed. B.C. Parker, 81–96. Lawrence, KS: Allen Press.Google Scholar
  21. Duke, N.C., M.C. Ball, and J.C. Ellison. 1998. Factors influencing biodiversity and distributional gradients in mangroves. Global Ecology and Biogeography Letters 7 (1): 27–47.Google Scholar
  22. Duke, N.C., J.M. Kovacs, A.D. Griffiths, L. Preece, D.J.E. Hill, P. van Oosterzee, J. Mackenzie, H.S. Morning, and D. Burrows. 2017. Large-scale dieback of mangroves in Australia’s Gulf of Carpentaria: a severe ecosystem response, coincidental with an unusually extreme weather event. Marine and Freshwater Research 68 (10): 1816–1829.Google Scholar
  23. Duke, N., C. Field, J. Mackenzie, J.-O. Meynecke, and A. Wood. 2019. Rainfall and its possible hysteresis effect on proportional cover of tropical tidal wetland mangroves and saltmarsh-saltpans. Marine and Freshwater Research 70 (8): 1047.  https://doi.org/10.1071/MF18321.CrossRefGoogle Scholar
  24. Dunton, K.H., B. Hardegree, and T.E. Whitledge. 2001. Response of estuarine marsh vegetation to interannual variations in precipitation. Estuaries and Coasts 24 (6): 851–861.Google Scholar
  25. Eleuterius, L.N. 1976. The distribution of Juncus roemerianus in the salt marshes of North America. Chesapeake Science 17 (4): 289–292.Google Scholar
  26. Ellison, A.M. 2019. Foundation species, non-trophic interactions, and the value of being common. iScience 13: 254–268.Google Scholar
  27. Ellison, A.M., M.S. Bank, B.D. Clinton, E.A. Colburn, K. Elliott, C.R. Ford, D.R. Foster, B.D. Kloeppel, J.D. Knoepp, G.M. Lovett, J. Mohan, D.A. Orwig, W.V. Sobczak, K.A. Stinson, J.K. Stone, C.M. Swan, J. Thompson, B. Von Holle, and J.R. Webster. 2005. Loss of foundation species: consequences for the structure and dynamics of forested ecosystems. Frontiers in Ecology and the Environment 3 (9): 479–486.Google Scholar
  28. Fariña, J.M., Q. He, B.R. Silliman, and M.D. Bertness. 2018. Biogeography of salt marsh plant zonation on the Pacific coast of South America. Journal of Biogeography 45 (1): 238–247.Google Scholar
  29. Feher, L.C., M.J. Osland, K.T. Griffith, J.B. Grace, R.J. Howard, C.L. Stagg, N.M. Enwright, K.W. Krauss, C.A. Gabler, R.H. Day, and K. Rogers. 2017. Linear and nonlinear effects of temperature and precipitation on ecosystem properties in tidal saline wetlands. Ecosphere 8 (10): e01956.Google Scholar
  30. Fosberg, F.R. 1961. Vegetation-free zone on dry mangrove coasts. U.S. Geological Survey Professional Paper 424-D: 216–218.Google Scholar
  31. Fourqurean, J.W., T.J. Smith III, J. Possley, T.M. Collins, D. Lee, and S. Namoff. 2010. Are mangroves in the tropical Atlantic ripe for invasion? Exotic mangrove trees in the forests of South Florida. Biological Invasions 12 (8): 2509–2522.Google Scholar
  32. Gabler, C.A., M.J. Osland, J.B. Grace, C.L. Stagg, R.H. Day, S.B. Hartley, N.M. Enwright, A.S. From, M.L. McCoy, and J.L. McLeod. 2017. Macroclimatic change expected to transform coastal wetland ecosystems this century. Nature Climate Change 7 (2): 142–147.Google Scholar
  33. Gosselink, J.G. 1984. The ecology of delta marshes of coastal Louisiana: a community profile. Washington, DC: U.S. Fish and Wildlife Service FWS/OBS-84/09.Google Scholar
  34. Holdridge, L.R. 1967. Life zone ecology. San Jose, Costa Rica: Tropical Science Center.Google Scholar
  35. Ibarra-Obando, S.E., M. Poumian-Tapia, and H.N. Morzaria-Luna. 2010. Long-term effects of tidal exclusion on salt marsh plain species at Estero de Punta Banda, Baja California. Estuaries and Coasts 33 (3): 753–768.Google Scholar
  36. Janousek, C.N., K.J. Buffington, K.M. Thorne, G.R. Guntenspergen, J.Y. Takekawa, and B.D. Dugger. 2016. Potential effects of sea-level rise on plant productivity: species-specific responses in northeast Pacific tidal marshes. Marine Ecology Progress Series 548: 111–125.Google Scholar
  37. Janousek, C.N., K.M. Thorne, and J.Y. Takekawa. 2019. Vertical zonation and niche breadth of tidal marsh plants along the northeast pacific coast. Estuaries and Coasts 42 (1): 85–98.Google Scholar
  38. Johnson, J.S., D.M. Cairns, and C. Houser. 2013. Coastal marsh vegetation assemblages of Galveston Bay: insights for the East Texas Chenier Plain. Wetlands 33 (5): 861–870.Google Scholar
  39. Jones, S.F., C.L. Stagg, K.W. Krauss, and M.W. Hester. 2016. Tidal saline wetland regeneration of sentinel vegetation types in the northern Gulf of Mexico: an overview. Estuarine, Coastal and Shelf Science 174: A1–A10.Google Scholar
  40. Josselyn, M. 1983. The ecology of San Francisco Bay tidal marshes: a community profile. Washington, DC: U.S. Fish and Wildlife Service.Google Scholar
  41. Kirwan, M.L., and G.R. Guntenspergen. 2012. Feedbacks between inundation, root production, and shoot growth in a rapidly submerging brackish marsh. Journal of Ecology 100 (3): 764–770.Google Scholar
  42. Kirwan, M.L., and J.P. Megonigal. 2013. Tidal wetland stability in the face of human impacts and sea-level rise. Nature 504 (7478): 53–60.Google Scholar
  43. Kirwan, M.L., and A.B. Murray. 2007. A coupled geomorphic and ecological model of tidal marsh evolution. Proceedings of the National Academy of Sciences 104 (15): 6118–6122.Google Scholar
  44. Kirwan, M.L., G.L. Guntenspergen, and J.T. Morris. 2009. Latitudinal trends in Spartina alterniflora productivity and the response of coastal marshes to global change. Global Change Biology 15 (8): 1982–1989.Google Scholar
  45. Langston, A.K., D.A. Kaplan, and C. Angelini. 2017. Predation restricts black mangrove (Avicennia germinans) colonization at its northern range limit along Florida’s Gulf Coast. Hydrobiologia 803 (1): 317–331.Google Scholar
  46. Longley, W.L. 1994. Freshwater inflows to Texas bays and estuaries: ecological relationships and methods for determination of needs. Austin, TX: Texas Water Development Board and Texas Parks and Wildlife Department.Google Scholar
  47. Lovelock, C.E., K.W. Krauss, M.J. Osland, R. Reef, and M.C. Ball. 2016. The physiology of mangrove trees with changing climate. In Tropical tree physiology: adaptations and responses in a changing environment, ed. G. Goldstein and L.S. Santiago, 149–179. New York, NY: Springer.Google Scholar
  48. Lovelock, C.E., I.C. Feller, R. Reef, S. Hickey, and M.C. Ball. 2017. Mangrove dieback during fluctuating sea levels. Scientific Reports 7 (1): 1680.Google Scholar
  49. Lugo, A.E., and C. Patterson-Zucca. 1977. The impact of low temperature stress on mangrove structure and growth. Tropical Ecology 18: 149–161.Google Scholar
  50. Maestre, F.T., R.M. Callaway, F. Valladares, and C.J. Lortie. 2009. Refining the stress-gradient hypothesis for competition and facilitation in plant communities. Journal of Ecology 97 (2): 199–205.Google Scholar
  51. McKee, K.L. 2011. Biophysical controls on accretion and elevation change in Caribbean mangrove ecosystems. Estuarine, Coastal and Shelf Science 91 (4): 475–483.Google Scholar
  52. McKee, K.L., I.A. Mendelssohn, and M.D. Materne. 2004. Acute salt marsh dieback in the Mississippi River deltaic plain: a drought-induced phenomenon? Global Ecology and Biogeography 13 (1): 65–73.Google Scholar
  53. Mendelssohn, I.A., and J.T. Morris. 2000. Eco-physiological controls on the productivity of Spartina alterniflora Loisel. In Concepts and controversies in tidal marsh ecology, ed. M.P. Weinstein and D.A. Kreeger, 59–80. Dordrecht: Springer.Google Scholar
  54. Méndez-Alonzo, R., J. López-Portillo, and V.H. Rivera-Monroy. 2008. Latitudinal variation in leaf and tree traits of the mangrove Avicennia germinans (Avicenniaceae) in the central region of the Gulf of Mexico. Biotropica 40 (4): 449–456.Google Scholar
  55. Millennium Ecosystem Assessment. 2005. Ecosystems and human well-being: synthesis. Washington, DC: Island Press.Google Scholar
  56. Mitsch, W.J., and J.G. Gosselink. 2007. Wetlands. New York, NY: John Wiley & Sons.Google Scholar
  57. Montagna, P.A., J.C. Gibeaut, and J.W. Tunnell Jr. 2007. South Texas climate 2100: coastal impacts. In The changing climate of South Texas 1900–2100: problems and prospects, impacts and implications, ed. J. Norwine and K. John, 57–77. Kingsville, TX: CREST-RESSACA. Texas A & M University.Google Scholar
  58. Montagna, P.A., T.A. Palmer, and J.B. Pollack. 2013. Hydrological changes and estuarine dynamics. New York, NY: Springer.Google Scholar
  59. Montagna, P.A., A.L. Sadovski, S.A. King, K.K. Nelson, T.A. Palmer, and K.H. Dunton. 2017. Modeling the effect of water level on the Nueces Delta marsh community. Wetlands Ecology and Management 25 (6): 731–742.Google Scholar
  60. Morris, J.T., P.V. Sundareshwar, C.T. Nietch, B. Kjerfve, and D.R. Cahoon. 2002. Responses of coastal wetlands to rising sea level. Ecology 83 (10): 2869–2877.Google Scholar
  61. Nixon, S.W. 1982. The ecology of New England high salt marshes: a community profile. Washington, DC: U.S. Fish and Wildlife Service, Office of Biological Services.Google Scholar
  62. Odum, W.E., C.C. McIvor, and T.J. Smith III. 1982. The ecology of mangroves of south Florida: a community profile. Washington, DC: U.S. Fish and Wildlife Service, Office of Biological Services FWS/OBS-81/24.Google Scholar
  63. Odum, W.E., T.J. Smith III, J.K. Hoover, and C.C. McIvor. 1984. The ecology of tidal freshwater marshes of the United States east coast: a community profile. Washington, DC: U.S. Fish and Wildlife Service.Google Scholar
  64. Ogburn, R.M., and E.J. Edwards. 2010. The ecological water-use strategies of succulent plants. In Advances in botanical research, 179–225. Burlington, MA: Eslevier Academic Press.Google Scholar
  65. Osland, M.J., N. Enwright, R.H. Day, and T.W. Doyle. 2013. Winter climate change and coastal wetland foundation species: salt marshes vs. mangrove forests in the southeastern United States. Global Change Biology 19 (5): 1482–1494.Google Scholar
  66. Osland, M.J., N. Enwright, and C.L. Stagg. 2014. Freshwater availability and coastal wetland foundation species: ecological transitions along a rainfall gradient. Ecology 95 (10): 2789–2802.Google Scholar
  67. Osland, M.J., N.M. Enwright, R.H. Day, C.A. Gabler, C.L. Stagg, and J.B. Grace. 2016. Beyond just sea-level rise: considering macroclimatic drivers within coastal wetland vulnerability assessments to climate change. Global Change Biology 22 (1): 1–11.Google Scholar
  68. Osland, M.J., L.C. Feher, K.T. Griffith, K.C. Cavanaugh, N.M. Enwright, R.H. Day, C.L. Stagg, K.W. Krauss, R.J. Howard, J.B. Grace, and K. Rogers. 2017. Climatic controls on the global distribution, abundance, and species richness of mangrove forests. Ecological Monographs 87 (2): 341–359.Google Scholar
  69. Osland, M.J., L.C. Feher, J. López-Portillo, R.H. Day, D.O. Suman, J.M. Guzmán Menéndez, and V.H. Rivera-Monroy. 2018a. Mangrove forests in a rapidly changing world: global change impacts and conservation opportunities along the Gulf of Mexico coast. Estuarine, Coastal and Shelf Science 214: 120–140.Google Scholar
  70. Osland, M.J., C.A. Gabler, J.B. Grace, R.H. Day, M.L. McCoy, J.L. McLeod, A.S. From, N.M. Enwright, L.C. Feher, C.L. Stagg, and S.B. Hartley. 2018b. Climate and plant controls on soil organic matter in coastal wetlands. Global Change Biology 24 (11): 5361–5379.Google Scholar
  71. Osland, M.J., R.H. Day, C.T. Hall, L.C. Feher, A.R. Armitage, J. Cebrian, K.H. Dunton, A.R. Hughes, D.A. Kaplan, A.K. Langston, A. Macy, C.A. Weaver, G.H. Anderson, K. Cummins, I.C. Feller, and C.M. Snyder. 2019. Temperature thresholds for black mangrove (Avicennia germinans) freeze damage, mortality, and recovery in North America: refining tipping points for range expansion in a warming climate. Journal of Ecology.  https://doi.org/10.1111/1365-2745.13285.
  72. Pecl, G.T., M.B. Araújo, J.D. Bell, J. Blanchard, T.C. Bonebrake, I.-C. Chen, T.D. Clark, R.K. Colwell, F. Danielsen, B. Evengård, L. Falconi, S. Ferrier, S. Frusher, R.A. Garcia, R.B. Griffis, A.J. Hobday, C. Janion-Scheepers, M.A. Jarzyna, S. Jennings, J. Lenoir, H.I. Linnetved, V.Y. Martin, P.C. McCormack, J. McDonald, N.J. Mitchell, T. Mustonene, J.M. Pandolfi, N. Pettorelli, E. Popova, S.A. Robinson, B.R. Scheffers, J.D. Shaw, C.J.B. Sorte, J.M. Strugnell, J.M. Sunday, N. Tuanmu, A. Verges, C. Villanueva, T. Wernberg, E. Wapstra, and S.E. Williams. 2017. Biodiversity redistribution under climate change: Impacts on ecosystems and human well-being. Science 355 (6332): eaai9214.Google Scholar
  73. Pennings, S.C., M. Alber, R.A. Clark, M. Booth, A. Burd, C. Wei-Jun, C. Craft, C.B. Depratter, D. Di Iorio, C.S. Hopkinson, S.B. Joye, C.D. Meile, W.S. Moore, B. Silliman, V. Thompson, and J.P. Wares. 2012. South Atlantic tidal wetlands. In Wetland habitats of North America: ecology and conservation concerns, ed. D.P. Batzer and A.H. Baldwin, 45–61. Berkeley, CA: University of California Press.Google Scholar
  74. Peterson, J.M., and S.S. Bell. 2012. Tidal events and salt-marsh structure influence black mangrove (Avicennia germinans) recruitment across and ecotone. Ecology 93 (7): 1648–1658.Google Scholar
  75. Pickens, C.N., T.M. Sloey, and M.W. Hester. 2019. Influence of salt marsh canopy on black mangrove (Avicennia germinans) survival and establishment at its northern latitudinal limit. Hydrobiologia 826 (1): 195–208.Google Scholar
  76. Rasser, M.K., N.L. Fowler, and K.H. Dunton. 2013. Elevation and plant community distribution in a microtidal salt marsh of the western Gulf of Mexico. Wetlands 33 (4): 575–583.Google Scholar
  77. Ridd, P., M.W. Sandstrom, and E. Wolanski. 1988. Outwelling from tropical tidal salt flats. Estuarine, Coastal and Shelf Science 26 (3): 243–253.Google Scholar
  78. Roman, C.T., N. Jaworski, F.T. Short, S. Findlay, and R.S. Warren. 2000. Estuaries of the northeastern United States: habitat and land use signatures. Estuaries 23 (6): 743–764.Google Scholar
  79. Ross, M.S., P.L. Ruiz, J.P. Sah, and E.J. Hanan. 2009. Chilling damage in a changing climate in coastal landscapes of the subtropical zone: a case study from south Florida. Global Change Biology 15 (7): 1817–1832.Google Scholar
  80. Saenger, P. 2002. Mangrove ecology, silviculture and conservation. Dodrecht: Springer.Google Scholar
  81. Saintilan, N. 2009. Biogeography of Australian saltmarsh plants. Austral Ecology 34 (8): 929–937.Google Scholar
  82. Seliskar, D.M., and J.L. Gallagher. 1983. The ecology of tidal marshes of the Pacific Northwest: a community profile. Washington, DC: U.S. Fish and Wildlife Service.Google Scholar
  83. Simard, M., L. Fatoyinbo, C. Smetanka, V.H. Rivera-Monroy, E. Castañeda-Moya, N. Thomas, and T. Van der Stocken. 2019. Mangrove canopy height globally related to precipitation, temperature and cyclone frequency. Nature Geoscience 12 (1): 40–45.Google Scholar
  84. Stout, J. 1984. The ecology of irregularly flooded salt marshes of the northeastern Gulf of Mexico: a community profile. Washington, DC: U.S. Fish and Wildlife Service Biological Report 85 (7.1).Google Scholar
  85. Strong, D.R., and D.R. Ayres. 2013. Ecological and evolutionary misadventures of Spartina. Annual Review of Ecology, Evolution, and Systematics 44 (1): 389–410.Google Scholar
  86. Takekawa, J.Y., K.M. Thorne, K.J. Buffington, C.M. Freeman, K.W. Powelson, and G. Block. 2013. Assessing marsh response from sea-level rise applying local site conditions: Humboldt Bay National Wildlife Refuge. Data Summary Report. USGS Western Ecological Research Center, Vallejo, CA. 44pp + Appendices. Google Scholar
  87. Teal, J.M. 1986. The ecology of regularly flooded salt marshes of New England: a community profile. Washington, DC: U.S. Fish and Wildlife Service.Google Scholar
  88. Thomson, J.A., D.A. Burkholder, M.R. Heithaus, J.W. Fourqurean, M.W. Fraser, J. Statton, and G.A. Kendrick. 2015. Extreme temperatures, foundation species, and abrupt ecosystem change: an example from an iconic seagrass ecosystem. Global Change Biology 21 (4): 1463–1474.Google Scholar
  89. Tomlinson, P.B. 1986. The botany of mangroves. New York, NY: Cambridge University Press.Google Scholar
  90. Tunnell, J.W., and F.W. Judd. 2002. The Laguna Madre of Texas and Tamaulipas. College Station, TX: Texas A&M University Press.Google Scholar
  91. USGCRP. 2017. Climate science special report: fourth national climate assessment, Volume I. Washington, DC: U.S. Global Change Research Program.Google Scholar
  92. Van der Stocken, T., D. Carroll, D. Menemenlis, M. Simard, and N. Koedam. 2019. Global-scale dispersal and connectivity in mangroves. Proceedings of the National Academy of Sciences 116 (3): 915–922.Google Scholar
  93. Vergés, A., P.D. Steinberg, M.E. Hay, A.G.B. Poore, A.H. Campbell, E. Ballesteros, K.L. Heck, D.J. Booth, M.A. Coleman, D.A. Feary, W. Figueira, T. Langlois, E.M. Marzinelli, T. Mizerek, P.J. Mumby, Y. Nakamura, M. Roughan, E. van Sebille, A. Sen Gupta, D.A. Smale, F. Tomas, T. Wernberg, and S.K. Wilson. 2014. The tropicalization of temperate marine ecosystems: climate-mediated changes in herbivory and community phase shifts. Proceedings of the Royal Society B: Biological Sciences 281 (1789): 20140846.Google Scholar
  94. Visser, J.M., C.E. Sasser, R.H. Chabreck, and R.G. Linscombe. 1998. Marsh vegetation types of the Mississippi River deltaic plain. Estuaries 21 (4): 818–828.Google Scholar
  95. Visser, J.M., C.E. Sasser, R.H. Chabreck, and R.G. Linscombe. 2000. Marsh vegetation types of the Chenier Plain, Louisiana, USA. Estuaries 23 (3): 318–327.Google Scholar
  96. Whittaker, R.H. 1970. Communities and ecosystems. New York, NY: The McMillan Company.Google Scholar
  97. Wiegert, R.G., and B.J. Freeman. 1990. Tidal marshes of the southeast Atlantic Coast: a community profile. Washington, DC: U.S. Fish and Wildlife Service.Google Scholar
  98. Wigand, C., and C.T. Roman. 2012. North Atlantic coastal tidal wetlands. In Wetland habitats of North America: ecology and conservation concerns, ed. D.P. Batzer and A.H. Baldwin, 13–28. Berkeley, CA: University of California Press.Google Scholar
  99. Withers, K. 2002. Wind-tidal flats. In The Laguna Madre of Texas and Tamaulipas, ed. J.W. Tunnell and F.W. Judd, 114–126. College Station, TX: Texas A&M University Press.Google Scholar
  100. Woodroffe, C.D., and J. Grindrod. 1991. Mangrove biogeography: the role of quaternary environmental and sea-level change. Journal of Biogeography 18 (5): 479–492.Google Scholar
  101. Zedler, J.B. 1982. The ecology of southern California coastal salt marshes: a community profile. U.S. Fish and Wildlife Service, Biological Services Program, Washington DC. FWS/OBS-81/54.Google Scholar
  102. Zedler, J.B., J. Covin, C. Nordby, P. Williams, and J. Boland. 1986. Catastrophic events reveal the dynamic nature of salt-marsh vegetation in Southern California. Estuaries 9 (1): 75–80.Google Scholar
  103. Zedler, J.B., J.C. Callaway, and G. Sullivan. 2001. Declining biodiversity: why species matter and how their functions might be restored in Californian tidal marshes: biodiversity was declining before our eyes, but it took regional censuses to recognize the problem, long-term monitoring to identify the causes, and experimental plantings to show why the loss of species matters and which restoration strategies might reestablish species. Bioscience 51: 1005–1017.Google Scholar
  104. Zomer, R.J., A. Trabucco, O. van Straaten, and D.A. Bossio. 2006. Carbon, land and water: a global analysis of the hydrologic dimensions of climate change mitigation through afforestation/reforestation. Colombo: International Water Management Institute.Google Scholar

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© This is a U.S. government work and its text is not subject to copyright protection in the United States; however, its text may be subject to foreign copyright protection 2019

Authors and Affiliations

  1. 1.Wetland and Aquatic Research CenterU.S. Geological SurveyLafayetteUSA
  2. 2.Patuxent Wildlife Research CenterU.S. Geological SurveyLaurelUSA
  3. 3.Western Ecological Research CenterU.S. Geological SurveyDavisUSA

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