Abstract
Subtropical black mangrove (Avicennia germinans) is expanding into higher latitudes and encroaching on existing temperate salt marshes with the potential to alter a variety of ecological processes. In the Mississippi River Delta (Louisiana, U.S.A.), wave-driven marsh edge erosion is on the order of meters per year and accounts for half of the total marsh loss. Here, we show that edge erosion is reduced by 40–60% when colonized by Avicennia as compared to salt marsh dominated by Spartina alterniflora. This reduction is associated with a greater soil shear strength, which in turn is driven by more live belowground biomass and deeper roots. Crucially, Avicennia reduces edge erosion only when well established, i.e., marshes with sparse Avicennia cover had similar edge erosion rates to those with Spartina, likely due to a shallower root biomass. Overall, climate-driven Avicennia expansion will not prevent marsh edge erosion, but can significantly slow it down. Avicennia could be used as a nature-based solution to slow the rate of edge erosion if it is planted inland allowing it 5–10 years to mature before being exposed along the marsh edge.
Data availability
The data analyzed during this study is available in the Dryad repository: https://doi.org/10.5061/dryad.02v6wwqh9. Data is also available upon request by email to the primary author. The primary author is Mike Rabalais.
References
Walther, G. et al. Ecological responses to recent climate change. Nature 416(6978), 389–395. https://doi.org/10.1038/416389 (2002).
Parmesan, C. Ecological and evolutionary responses to recent climate change. Annu. Rev. Ecol. Evol. Syst. 37, 637–669. https://doi.org/10.1146/annurev.ecolsys.37.091305.110100 (2006).
Walther, G. Community and ecosystem response to recent climate change. Philos. Trans. R. Soc. B 365(1549), 2019–2024. https://doi.org/10.1098/rstb.2010.0021 (2010).
Verges, A. et al. The tropicalization of temperate marine ecosystems: Climate-mediated changes in herbivory and community phase shifts. Proc. R. Soc. B 281(1789), 20140846. https://doi.org/10.1098/rspb.2014.0846 (2014).
Osland, M. J., Enwright, N., Day, R. H. & Doyle, T. W. Winter climate change and coastal wetland foundation species: Salt marshes vs mangrove forests in the southeastern United States. Glob. Change Biol. 19(5), 1482–1494. https://doi.org/10.1111/gcb.12126 (2013).
Cavanaugh, K. C. et al. Poleward expansion of mangroves is a threshold response to decreased frequency of extreme cold events. Proc. Natl. Acad. Sci. U.S.A. 111(2), 723–727. https://doi.org/10.1073/pnas.1315800111 (2014).
Osland, M. J., Day, R. H., Hall, C. T., Brumfield, M. D. & Dugas, J. L. Mangrove expansion and contraction at a poleward range limit: Climate extremes and land-ocean temperature gradients. Ecology 98(1), 125–137. https://doi.org/10.1002/ecy.1625 (2016).
Kelleway, J. J. et al. Review of the ecosystem service implications of mangrove encroachment into salt marshes. Glob. Change Biol. 23(10), 3967–3983. https://doi.org/10.1111/gcb.13727 (2017).
Osland, M. J. et al. The impacts of mangrove range expansion on wetland ecosystem services in the southeastern United States: Current understanding, knowledge gaps, and emerging research needs. Glob. Change Biol. 28(10), 3163–3187. https://doi.org/10.1111/gcb.16111 (2022).
Doughty, C. L. et al. Mangrove range expansion rapidly increases coastal wetland carbon storage. Estuaries Coasts 39(2), 385–396. https://doi.org/10.1007/s12237-015-9993-8 (2016).
Comeaux, R. S., Allison, M. A. & Bianchi, T. S. Mangrove expansion in the Gulf of Mexico with climate change: Implications for wetland health and resistance to rising sea levels. Estuar. Coast. Shelf Sci. 96, 81–95. https://doi.org/10.1016/j.ecss.2011.10.003 (2012).
Charles, S. P. et al. Quantifying how changing mangrove cover affects ecosystem carbon storage in coastal wetlands. Ecology 101(2), e02916. https://doi.org/10.1002/ecy.2916 (2019).
Valentine, K. & Mariotti, G. Wind-driven water level fluctuations drive marsh edge erosion variability in microtidal coastal bays. Cont. Shelf Res. 176, 76–89. https://doi.org/10.1016/j.csr.2019.03.002 (2019).
Valentine, K., Bruno, G., Elsey-Quirk, T. & Mariotti, G. Brackish marshes erode twice as fast as saline marshes in the Mississippi Delta region. Earth Surf. Proc. Land. 46(9), 1739–1749. https://doi.org/10.1002/esp.5108 (2021).
Pennings, S. C., Glazner, R. M., Hughes, Z. J., Kominoski, J. S. & Armitage, A. R. Effects of mangrove cover on coastal erosion during a hurricane in Texas USA. Ecology https://doi.org/10.1002/ecy.3309 (2021).
Doughty, C. L., Cavanaugh, K. C., Hall, C. R., Feller, I. C. & Chapman, S. K. Impacts of mangrove encroachment and mosquito impoundment management on coastal protection services. Hydrobiologia 803(1), 105–120. https://doi.org/10.1007/s10750-017-3225-0 (2017).
Hijuelos, A. C. et al. Linking management planning for coastal wetlands to potential future wave attenuation under a range of relative sea-level rise scenarios. PLoS ONE https://doi.org/10.1371/journal.pone.0216695 (2019).
Leonardi, N., Ganju, N. K. & Fagherazzi, S. A linear relationship between wave power and erosion determines salt-marsh resilience to violent storms and hurricanes. Proc. Natl. Acad. Sci. 113(1), 64–68. https://doi.org/10.1073/pnas/1510095112 (2016).
Sapkota, Y. & White, J. R. Marsh edge erosion and associated carbon dynamics in coastal Louisiana: A proxy for future wetland-dominated coastlines world-wide. Estuar. Coast. Shelf Sci. 226(1), 106289. https://doi.org/10.1016/j.ecss.2019.106289 (2019).
Gillen, M. N., Messerschmidt, T. C. & Kirwan, M. L. Biophysical controls of marsh soil shear strength along an estuarine salinity gradient. Earth Surf. Dyn. 9, 413–421. https://doi.org/10.5194/esurf-9-413-2021 (2021).
Howes, N. C. et al. Hurricane-induced failure of low salinity wetlands. Proc. Natl. Acad. Sci. 107(32), 14014–14019. https://doi.org/10.1073/pnas.0914582107 (2010).
Sasser, C. E. et al. Relationships of marsh soil strength to belowground vegetation biomass in louisiana coastal marshes. Wetlands 38(2), 401–409. https://doi.org/10.1007/s13157-017-0977-2 (2017).
Hollis, L. O. & Turner, R. E. The tensile root strength of five emergent coastal macrophytes. Aquat. Bot. 146, 39–47. https://doi.org/10.1016/j.aquabot.2018.01.004 (2018).
Weaver, C. A. & Armitage, A. R. Above- and belowground responses to nutrient enrichment within a marsh-mangrove ecotone. Estuarine, Coastal Shelf Sci. 243, 106884. https://doi.org/10.1016/j.ecss.2020.106884 (2020).
Bianchi, T. S. et al. Historical reconstruction of mangrove expansion in the Gulf of Mexico: Linking climate change with carbon sequestration in coastal wetlands. Estuar. Coast. Shelf Sci. 119, 7–16. https://doi.org/10.1016/j.ecss.2012.12.007 (2013).
Giri, C., Long, J. & Tieszen, L. Mapping and monitoring louisiana’s mangroves in the aftermath of the 2010 gulf of mexico oil spill. J. Coastal Res. 27(6), 1059–1064. https://doi.org/10.2112/JCOASTRES-D-11-00028.1 (2011).
Rodrigues, E. et al. The effect of global warming on the establishment of mangroves in coastal Louisiana during the Holocene. Geomorphology 381, 107648. https://doi.org/10.1016/j.geomorph.2021.10764 (2021).
Couvillion, B.R., Beck, H., Schoolmaster, D., Fischer, M. Land area change in coastal Louisiana 1932 to 2016. U.S. Geological Survey Scientific Investigations Map 3381, 16 p. pamphlet. https://doi.org/10.3133/sim3381 (2017).
Blum, M. & Roberts, H. Drowning of the Mississippi Delta due to insufficient sediment supply and global sea-level rise. Nature Geosci. 2, 488–491. https://doi.org/10.1038/ngeo553 (2009).
Blum, M. & Roberts, H. The mississippi delta region: Past, present, and future. Annu. Rev. Earth Planet. Scie. 40, 655–683. https://doi.org/10.1146/annurev-earth-042711-105248 (2012).
Blum, M., Rahn, D., Frederick, B. & Polanco, S. Land loss in the Mississippi River Delta: Role of subsidence, global sea-level rise, and coupled atmospheric and oceanographic processes Global Planet. Change https://doi.org/10.1016/j.gloplacha.2023.104048 (2023).
Everett, T. C., Chen, Q., Karimpour, A. & Twilley, R. Quantification of swell energy and its impact on wetlands in a deltaic estuary. Estuaries Coasts 42(1), 68–84. https://doi.org/10.1007/s12237-018-0454-z (2019).
Francalanci, S., Bendoni, M., Rinaldi, M. & Solari, L. Ecomorphodynamic evolution of salt marshes: Experimental observation of bank retreat processes. Geomorphology 195(53), 65. https://doi.org/10.1016/j.geomorph.2013.04.026 (2013).
Schwimmer, R. A. Rates and processes of marsh shoreline erosion in Rehobath Bay, Delaware, USA. J. Coastal Res. 17(3), 672–683 (2001).
Perry, C. L. & Mendelssohn, I. A. Ecosystem effects of expanding populations of Avicennia germinans in a Louisiana salt marsh. Wetlands 29(1), 396–406. https://doi.org/10.1672/08-100.1 (2009).
McKee, K. L. & Vervaeke, W. C. Will fluctuations in salt marsh-mangrove dominance alter vulnerability of a subtropical wetland to sea level rise?. Glob. Change Biol. 24(3), 1224–1238 (2017).
Lovelock, C. E., Bennion, V., Grinham, A. & Cahoon, D. R. The role of surface and subsurface processes in keeping pace with sea level rise in intertidal wetlands of Moreton Bay, Queensland, Australia. Ecosystems 14, 745–757 (2011).
Saintilan, N. et al. Vertical accretion trends in Australian tidal wetlands. Estuaries Coasts 47, 2057–2070. https://doi.org/10.1007/s12237-023-01267-x (2024).
Gallagher, J. L. & Plumley, F. G. Underground biomass profiles and productivity in Atlantic coastal marshes. Am. J. Bot. 66(2), 156–161. https://doi.org/10.1002/j.1537-2197.1979.tb06208.x (1979).
Gross, M. F., Hardisky, M. A., Wolf, P. L. & Klemas, V. Relationship between aboveground and belowground biomass of Spartina alterniflora (smooth cordgrass). Estuaries 14, 180–191. https://doi.org/10.2307/1351692 (1991).
Blum, L. K. Spartina alterniflora root dynamics in a Virginia marsh. Mar. Ecol. Prog. Ser. 102, 169–178. https://doi.org/10.3354/meps102169 (1993).
Darby, F. A. & Turner, R. E. Below and aboveground Spartina alterniflora production in a Louisiana salt marsh. Estuaries Coasts 31(223–231), 2008. https://doi.org/10.1007/s12237-008-9037-8 (2008).
Conroy, B. M., Kelleway, J. J. & Rogers, K. Root productivity contributes to carbon storage and surface elevation adjustments in coastal wetlands. Plant Soil. 513, 605–631. https://doi.org/10.1007/s11104-025-07204-0 (2025).
Pezeshki, S. R. Root responses of flood-tolerant and flood-sensitive tree species to soil redox conditions. Trees 5, 180–186. https://doi.org/10.1007/BF00204341 (1991).
Madhavan, C., Meera, S. P. & Kumar, A. Anatomical adaptations of mangroves to the intertidal environment and their dynamic responses to various stresses. Biol. Rev. 100, 1019–1046. https://doi.org/10.1111/brv.13172 (2025).
Srikanth, S., Lum, S. K. Y. & Chen, Z. Mangrove root: Adaptations and ecological importance. Trees 30, 451–465. https://doi.org/10.1007/s00468-015-1233-0 (2016).
Niklas, K.J. Spatz, H.C. Plant physics. University of Chicago Press, (2012).
Ladd, C. J. T., Duggan-Edwards, M. F., Bouma, T. J., Pages, J. F. & Skov, M. W. Sediment supply explains long-term and large-scale patterns in salt marsh lateral expansion and erosion. Geophys. Res. Lett. 46(20), 11178–11187. https://doi.org/10.1029/2019GL083315 (2019).
Pickens, C. N. & Hester, M. W. Temperature tolerance of early life history stages of black mangrove Avicennia germinans: Implications for range expansion. Estuaries Coasts 34(4), 396–406. https://doi.org/10.1007/s12237-101-9358-2 (2011).
Osland, M. J. et al. Life stage influences the resistance and resilience of black mangrove forests to winter climate extremes. Ecosphere https://doi.org/10.1890/ES15-00042.1 (2015).
Chimner, R. A., Fry, B., Kaneshiro, M. Y. & Cormier, N. Current extent and historical expansion of introduced mangroves on O’ahu. Hawai’i. Pacific Science. 60(3), 377–383. https://doi.org/10.1353/psc.2006.0013 (2006).
Lundquist, C. J., Morrisey, D. J., Gladstone-Gallagher, R. V. & Swales, A. Managing mangrove habitat expansion in New Zealand. In Mangrove Ecosystems of Asia: status, challenges and management strategies 415–438 (New York, NY, Springer, New York, 2013).
Horstman, E. M., Lundquist, C.J., Bryan, K.B., Bulmer, R.H., Mullarney, J.C., Stokes, D.J. The dynamics of expanding mangroves in New Zealand. https://doi.org/10.1007/978-1-4614-8582-7_19 (2014).
Alleman, L. K. & Hester, M. W. Refinement of the fundamental niche of black mangrove seedlings (Avicennia germinans) in Louisiana: Applications for restoration. Wetlands Ecol. Manage. 19(1), 47–60. https://doi.org/10.1007/s11273-010-919906 (2011).
Madison, M.J., Mack, S.K., Lane, R.R., Day, J.W. Wetland restoration using mangroves in southern Louisiana. in Paper Presented at the SPE Americas E&P Health Safety Security and Environmental Conference in Galveston, TX. https://doi.org/10.2118/163789-MS (2013).
Yando, E. S., Osland, M. J., Jones, S. F. & Hester, M. W. Jump-starting coastal wetland restoration: A comparison of marsh and mangrove foundation species. Restor. Ecol. 27(5), 1145–1154. https://doi.org/10.1111/rec.12963 (2019).
Miller, C. B., Rodriguez, A. B. & Bost, M. C. Sea-level rise, localized subsidence, and increased storminess promote saltmarsh transgression across low-gradient upland areas. Quatern. Sci. Rev. https://doi.org/10.1016/j.quascirev.2021.107000 (2021).
Coastal Protection and Restoration Authority of Louisiana (CPRA). Louisiana’s comprehensive Master Plan for a sustainable coast. Coastal Protection and Restoration Authority. Baton Rouge, LA. (2023).
Wang, J. J., Li, X. Z., Lin, S. W. & Ma, Y. X. Economic evaluation and systematic review of salt marsh restoration projects at a global scale. Front. Ecol. Evol. https://doi.org/10.3389/fevo.2022.865516 (2021).
Karimpour, A., Chen, Q, Jadhav, R. Turbidity dynamics in upper Terrebonne Bay, Louisiana. Sediment Transport: Monitoring, Modeling and Management, Nova Sc. Pub. 339–360 (1996).
Young, I. R. & Verhagen, L. A. The growth of fetch limited waves in water of finite depth. Part 1. Total energy and peak frequency. Coast. Eng. 29, 47–78. https://doi.org/10.1016/S0378-3839(96)00006-3 (1996).
Merrill, J., Mariotti, G., Li, C. & Hiatt, M. Impacts of tropical cyclones on wave and current regime in a shallow, microtidal bay. Cont. Shelf Res. 273, 105182. https://doi.org/10.1016/j.csr.2024.105182 (2024).
Mariotti, G. et al. Biased wind measurements in estuarine waters. J. Geophys. Res.: Oceans 123(5), 3577–3587. https://doi.org/10.1029/2017JC013748 (2018).
Seago, J. L. Jr. et al. A re-examination of the root cortex in wetland flowering plants with respect to aerenchyma. Ann. Bot. 96(4), 565–579. https://doi.org/10.1093/aob/mci211 (2003).
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This work was supported by the National Science Foundation under award GEO/EAR 2126167.
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MR wrote the main manuscript text and prepared Figs. 1, 3, 4, 5, 6, and 7. EE and GM prepared Table 1 and Fig. 2. MR, TQ, and GM reviewed the manuscript.
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All applicable international, national, and/or institutional guidelines were followed by the authors. Plant samples were collected from publicly accessible sites. Site access permits needed were obtained, and no threatened or endangered species were collected. Avicennia germinans is listed as an IUCN Red List Species of Least Concern and Spartina alterniflora has no regulations or restrictions for collection.
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Rabalais, M., Elmer, E., Quirk, T.E. et al. Climate-driven Avicennia germinans expansion reduces marsh edge erosion in coastal Louisiana (USA).
Sci Rep (2026). https://doi.org/10.1038/s41598-026-39843-3
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DOI: https://doi.org/10.1038/s41598-026-39843-3
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