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Palynological reconstruction of environmental changes in coastal wetlands of the Florida Everglades since the mid-Holocene

Published online by Cambridge University Press:  20 January 2017

Qiang Yao ,
Kam-biu Liu ,
William J. Platt  and
Victor H. Rivera-Monroy
Qiang Yao*
Affiliation:
Department of Oceanography and Coastal Sciences, School of the Coast and Environment, Louisiana State University, Baton Rouge, LA 70803, USA
Kam-biu Liu
Affiliation:
Department of Oceanography and Coastal Sciences, School of the Coast and Environment, Louisiana State University, Baton Rouge, LA 70803, USA
William J. Platt
Affiliation:
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA
Victor H. Rivera-Monroy
Affiliation:
Department of Oceanography and Coastal Sciences, School of the Coast and Environment, Louisiana State University, Baton Rouge, LA 70803, USA
*
*Corresponding author at: Department of Oceanography and Coastal Sciences, Louisiana State University, Baton Rouge, LA 70803, USA. Fax: + 1 225 578 6423. E-mail address:[email protected] (Q. Yao).
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Abstract

Palynological, loss-on-ignition, and X-ray fluorescence data from a 5.25 m sediment core from a mangrove forest at the mouth of the Shark River Estuary in the southwestern Everglades National Park, Florida were used to reconstruct changes occurring in coastal wetlands since the mid-Holocene. This multi-proxy record contains the longest paleoecological history to date in the southwestern Everglades. The Shark River Estuary basin was formed ~ 5700 cal yr BP in response to increasing precipitation. Initial wetlands were frequently-burned short-hydroperiod prairies, which transitioned into long-hydroperiod prairies with sloughs in which peat deposits began to accumulate continuously about 5250 cal yr BP. Our data suggest that mangrove communities started to appear after ~ 3800 cal yr BP; declines in the abundance of charcoal suggested gradual replacement of fire-dominated wetlands by mangrove forest over the following 2650 yr. By ~ 1150 cal yr BP, a dense Rhizophora mangle dominated mangrove forest had formed at the mouth of the Shark River. The mangrove-dominated coastal ecosystem here was established at least 2000 yr later than has been previously estimated.

Keywords

Shark River EstuaryEvergladesFloridaMangrovesPollenShort- and long-hydroperiod prairieWetlands
Type
Original Articles
Information
Quaternary Research , Volume 83 , Issue 3 , May 2015 , pp. 449 - 458
Copyright
University of Washington

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References

Armentano, T.V., Doren, R.F., Platt, W.J., and Mullins, T. (1995). Effects of Hurricane Andrew on coastal and interior forests of southern Florida. Journal of Coastal Research 21, 111–144.Google Scholar
Barr, J.G., Engel, V., Smith, T.J., and Fuentes, J.D. (2012). Hurricane disturbance and recovery of energy balance, CO2 fluxes and canopy structure in a mangrove forest of the Florida Everglades. Agricultural and Forest Meteorology 153, 54–66.CrossRefGoogle Scholar
Beckage, B., Platt, W.J., Slocum, M.G., and Panko, B. (2003). Influence of the El Niño-Southern Oscillation on the fire regimes of the Florida Everglades. Ecology 84, 3124–3130.CrossRefGoogle Scholar
Behling, H., Cohen, M.C.L., and Lara, R.J. (2001). Studies on Holocene mangrove ecosystem dynamics of the Braganc, a Peninsula in north-eastern Pará, Brazil. Palaeogeography, Palaeoclimatology, Palaeoecology 167, 225–242.CrossRefGoogle Scholar
Bernhardt, C.E., and Willard, D.A. (2009). Response of the Everglades ridge and slough landscape to climate variability and 20th-century water management. Ecological Applications 19, 1723–1738.CrossRefGoogle ScholarPubMed
Blaauw, M., and Christen, J.A. (2013). BACON Manual. http://chrono.qub.ac.uk/blaauw/.Google Scholar
Casta"eda-Moya, E., Twilley, R.R., Rivera-Monroy, V.H., Zhang, K.Q., Davis, S.E., and Ross, M. (2010). Sediment and nutrient deposition associated with Hurricane Wilma in mangroves of the Florida Coastal Everglades. Estuaries and Coasts 33, 45–58.CrossRefGoogle Scholar
Castañeda-Moya, E., Twilley, R.R., and Rivera-Monroy, V.H. (2013). Allocation of biomass and net primary productivity of mangrove forests along environmental gradients in the Florida Coastal Everglades, USA. Forest Ecology and Management 307, 226–241.CrossRefGoogle Scholar
Chappell, J.M.A., and Grindrod, J. (1985). Pollen analysis: a key to past mangrove communities and successional changes in North Australian coastal environments. Bardsley, K.N., Davie, J.D.S., Woodroffe, C.D. Coasts and Tidal Wetlands of the Australian Monsoon Region Australian National University, Canberra.225–236.Google Scholar
Chen, R., and Twilley, R.R. (1999a). A simulation model of organic matter and nutrient accumulation in mangrove wetland soils. Biogeochemistry 44, 93–118.CrossRefGoogle Scholar
Chen, R., and Twilley, R.R. (1999b). Patterns of mangrove forest structure and soil nutrient dynamics along the Shark River Estuary, Florida. Estuaries 22, 955–970.CrossRefGoogle Scholar
Chmura, G.L., Stone, P.A., and Ross, M.S. (2006). Non-pollen microfossils in Everglades sediments. Review of Palaeobotany and Palynology 141, 103–119.CrossRefGoogle Scholar
Davison, W. (1988). Interactions of iron, carbon and sulphur in marine and lacustrine sediments. Geological Society, London, Special Publications 40, 131–137.CrossRefGoogle Scholar
Dean, W.E. Jr. (1974). Determination of carbonate and organic matter in calcareous sediments and sedimentary rocks by loss on ignition: comparison with other methods. Journal of Sedimentary Petrology 44, 242–248.Google Scholar
DeCoster, J., Platt, W.J., and Riley, S.A. (1999). Pine savannas of Everglades National Park: an endangered ecosystem. Jones, D.T., Gamble, W.B. Florida's Garden of Good and Evil, Proceedings of the 1998 Joint Symposium of the Florida Exotic Pest Plant Council and the Florida Native Plant Society South Florida Water Management District, West Palm Beach, Florida.81–88.Google Scholar
Donders, T.H., Wagner, F., Dilcher, D.L., and Visscher, H. (2005). Mid- to late-Holocene El Niño-Southern Oscillation dynamics reflected in the subtropical terrestrial realm. Proceedings of the National Academy of Sciences 102, 10,904–10,908.CrossRefGoogle ScholarPubMed
Doren, R.F., Platt, W.J., and Whiteaker, L.D. (1993). Density and size structure of slash pine stands in the everglades region of south Florida. Forest Ecology and Management 59, 295–311.CrossRefGoogle Scholar
Ellison, J.C. (2008). Long-term retrospection on mangrove development using sediment cores and pollen analysis: a review. Aquatic Botany 89, 93–104.CrossRefGoogle Scholar
Gaiser, E.E., McCormick, P.V., Hagerthey, S.E., and Gottlieb, A.D. (2011). Landscape patterns of periphyton in the Florida Everglades. Critical Reviews in Environmental Science and Technology 41, 92–120.CrossRefGoogle Scholar
Gill, A.M., and Tomlinson, P.B. (1977). Studies on the growth of red mangrove (Rhizophora mangle L.) 1. Habit and general morphology. Biotropica 1, 1–9.CrossRefGoogle Scholar
Gleason, P.J., and Stone, P.A. (1994). Age, origin and landscape evolution of the Everglades peatland. Davis, S.M., Ogden, J.C. Everglades, the Ecosystem and its Restoration St. Lucie Press, Delray Beach, FL.149–198.Google Scholar
Gonzalez, C., Urrego, L.E., Martinez, J.I., Polania, J., and Yokoyama, Y. (2010). Mangrove dynamics in the southwestern Caribbean since the “Little Ice Age”: a history of human and natural disturbances. Holocene 20, 849–861.CrossRefGoogle Scholar
Hanan, E.J., Ross, M.S., and Ruiz, P.L. (2010). Multi-scaled grassland-woody plant dynamics in the heterogeneous marl prairies of the Southern Everglades. Ecosystems 13, 1256–1274.CrossRefGoogle Scholar
Hine, A.C., and Belknap, D.F. (1986). Recent geological history and modem sedimentary processes of the Pasco, Hemando and Citrus County coastline: west central Florida. Florida Sea Grant Report 79, University of Florida, Gainesville, Fl..166.Google Scholar
Intergovernmental Panel on Climate Change (IPCC), (2014). Climate change 2013: the scientific basis. Solomon, S. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change Cambridge Univ. Press, New York.Google Scholar
Islebe, G., Hooghiemstra, H., Brenner, M., Curtis, J., and Hodell, D. (1996). A Holocene vegetation history from lowland Guatemala. The Holocene 6, 265–271.CrossRefGoogle Scholar
Kiage, L.M., and Liu, K.B. (2009). Palynological evidence of climate change and land degradation in the Lake Baringo area, Kenya, East Africa, since AD 1650. Palaeogeography, Palaeoclimatology, Palaeoecology 279, 60–72.CrossRefGoogle Scholar
Koutavas, A., Lynch-Stieglitz, J., Marchitto, T.M. Jr., and Sachs, J.P. (2002). El Niño-like pattern in ice age tropical Pacific sea surface temperature. Science 297, 226–230.CrossRefGoogle ScholarPubMed
Kropp, W. (1976). Geochronology of corkscrew swamp sanctuary. In: Cypress Wetlands for Water Management, Recycling and Conservation, University of Florida, Gainesville.772–785.Google Scholar
Light, S.S., and Dineen, J.W. (1994). Water control in the Everglades: a historical perspective. Davis, S.M., Ogden, J.C. Everglades: The Ecosystem and Its Restoration St. Lucie Press, Delray Beach, Florida.47–84.Google Scholar
Liu, K.B., Li, C., Bianchette, T.A., McCloskey, T.A., Yao, Q., and Weeks, E. (2011). Storm deposition in a coastal backbarrier lake in Louisiana caused by Hurricanes Gustav and Ike. Journal of Coastal Research Special Issue 64, 1866–1870.Google Scholar
Lodge, T.E. (2010). The Everglades Handbook: Understanding the Ecosystem. second editionCRC Press, Boca Raton, Florida.Google Scholar
Macintyre, I.G., Toscano, M.A., Lighty, R.G., and Bond, G.B. (2004). Holocene history of the mangrove islands of Twin Cays, Belize, Central America. Atoll Research Bulletin 510, 1–16.Google Scholar
McAndrews, J.H., Berti, A.A., and Norris, G. (1973). Key to the Quaternary pollen and spores of the Great Lakes region. Life Science Miscellaneous Publication vol. 64, Royal Ontario Museum, .Google Scholar
Michot, B., Meselhe, E.A., Rivera-Monroy, V.H., Coronado-Molina, C., and Twilley, R.R. (2011). A tidal creek water budget: estimation of groundwater discharge and overland flow using hydrologic modeling in the Southern Everglades. Estuarine, Coastal and Shelf Science 93, 438–448.CrossRefGoogle Scholar
Miller, R. (1945). The heavy minerals of Florida beach and dune sands. American Mineralogist 30, 65–75.Google Scholar
Monacci, N.M., Meier-Grünhagen, U., Finney, B.P., Behling, H., and Wooller, M.J. (2009). Mangrove ecosystem changes during the Holocene at Spanish Lookout Cay, Belize. Palaeogeography, Palaeoclimatology, Palaeoecology 280, 37–46.CrossRefGoogle Scholar
Parkinson, R.W. (1989). Decelerating Holocene sea-level rise and its influence on southwest Florida Coastal evolution: a transgressive/regressive stratigraphy. Journal of Sedimentary Petrology 59, 960–972.Google Scholar
Platt, W.J. (1999). Southeastern pine savannas. Anderson, R.C., Fralish, J.S., Baskin, J. The Savanna, Barren, and Rock Outcrop Communities of North America Cambridge University Press, Cambridge, England.23–51.CrossRefGoogle Scholar
Platt, W.J., Orzell, S.L., and Slocum, M.G. (2015). Seasonality of fire weather strongly influences fire regimes in south Florida savanna-grassland landscapes. PLoS ONE 10, 1, e0116952.CrossRefGoogle ScholarPubMed
Ramírez-Herrera, M.T., Lagos, M., Hutchinson, I., Kostoglodov, V., Machain, M.L., Caballero, M., Goguitchaichvili, A., Aguilar, B., Chagu"-Goff, C., Goff, J., Ruiz-Fernández, A.C., Ortiz, M., Nava, H., Bautista, F., Lopez, G.I., and Quintana, P. (2012). Extreme wave deposits on the Pacific coast of Mexico: tsunami or storms? A multi-proxy approach. Geomorphology 140, 360–371.CrossRefGoogle Scholar
Rivera-Monroy, V.H., Twilley, R.R., Davis, S.E., Childers, D.L., Simard, M., Chambers, R., Jaffe, R., Boyer, J.N., Rudnick, D.T., Zhang, K., Castaneda-Moya, E., Ewe, S.M.L., Price, R.M., Coronado-Molina, C., Ross, M., Smith, T.J., Michot, B., Meselhe, E., Nuttle, W., Troxler, T.G., and Noe, G.B. (2011). The role of the Everglades Mangrove Ecotone Region (EMER) in regulating nutrient cycling and wetland productivity in South Florida. Critical Reviews in Environmental Science and Technology 41, 633–669.CrossRefGoogle Scholar
Robbin, D.M. (1984). A new Holocene sea level curve for the upper Florida Keys and Florida reef tract. Gleason, P.J. Environments of South Florida, Present and Past II 2nd ed.Miami Geological Society, 437–458.Google Scholar
Rodbell, D.T., Seltzer, G.O., Anderson, D.M., Abbott, M.B., Enfield, D.B., and Newman, J.H. (1999). An 15,000-year record of El Niño-driven alluviation in southwestern Ecuador. Science 283, 516–520.CrossRefGoogle ScholarPubMed
Ross, M.S., Meeder, J.F., Sah, J.P., Ruiz, P.L., and Telesnicki, G.J. (2000). The southeast saline Everglades revisited: 50 years of coastal vegetation change. Journal of Vegetation Science 11, 101–112.CrossRefGoogle Scholar
Ross, M.S., O'Brien, J.J., Ford, R.G., Zhang, K.Q., and Morkill, A. (2009). Disturbance and the rising tide: the challenge of biodiversity management on low-island ecosystems. Frontiers in Ecology and Environment 7, 471–478.CrossRefGoogle Scholar
Sabatier, P., Dezileau, L., Condomines, M., Briqueu, L., Colin, C., Bouchette, F., Le Duff, M., and Blanchemanche, P. (2008). Reconstruction of paleostorm events in a coastal lagoon (Herault, South of France). Marine Geology 251, 224–232.CrossRefGoogle Scholar
Saha, A.K., Moses, C.S., Price, R.M., Engel, V., Smith, T.J., and Anderson, G. (2012). A hydrological budget (2002–2008) for a large subtropical wetland ecosystem indicates marine groundwater discharge accompanies diminished freshwater flow. Estuaries and Coasts 35, 459–474.CrossRefGoogle Scholar
Schmitz, M., Platt, W.J., and DeCoster, J. (2002). Substrate heterogeneity and numbers of plant species in Everglades savannas (Florida, USA). Plant Ecology 160, 137–148.CrossRefGoogle Scholar
Scholl, D.W., Craighead, F.C., and Stuiver, M. (1969). Florida submergence curve revisited: its relation to coastal sedimentation rates. Science 163, 562–564.CrossRefGoogle Scholar
Scott, D.B., Collins, E.S., Gayes, P.T., and Wright, E. (2003). Records of prehistoric hurricanes on the South Carolina coast based on micropaleontological and sedimentological evidence, with comparison to other Atlantic Coast records. Geological Society of America Bulletin 115, 1027–1039.CrossRefGoogle Scholar
Scourse, J., Marret, F., Versteegh, G.J.M., Jansen, J.H.F., Schefuss, E., and van der Plicht, J. (2005). High-resolution last deglaciation record from the Congo fan reveals significance of mangrove pollen and biomarkers as indicators of shelf transgression. Quaternary Research 64, 57–69.CrossRefGoogle Scholar
Simard, M., Zhang, K.Q., Rivera-Monroy, V.H., Ross, M.S., Ruiz, P.L., Castañeda-Moya, E., Twilley, R.R., and Rodriguez, E. (2006). Mapping height and biomass of mangrove forests in Everglades National Park with SRTM elevation data. Photogrammetric Engineering and Remote Sensing 72, 299–311.CrossRefGoogle Scholar
Slocum, M.G., Platt, W.J., and Cooley, H.C. (2003). Effects of differences in prescribed fire regimes on patchiness and intensity of fires in subtropical savannas of Everglades National Park, Florida. Restoration Ecology 11, 91–102.CrossRefGoogle Scholar
Slocum, M.G., Platt, W.J., Beckage, B., Panko, B., and Lushine, J.B. (2007). Decoupling natural and anthropogenic fire regimes: a case study in Everglades National Park, Florida. Natural Areas Journal 27, 41–55.CrossRefGoogle Scholar
Slocum, M.G., Platt, W.J., Beckage, B., Orzell, S.L., and Taylor, W. (2010). Accurate quantification of seasonal rainfall and associated climate-wildfire relationships. Journal of Applied Meteorology and Climatology 49, 2559–2573.CrossRefGoogle Scholar
Smith, T.J., Anderson, G.H., Balentine, K., Tiling, G., Ward, G.A., and Whelan, K.R.T. (2009). Cumulative impacts of hurricanes on Florida mangrove ecosystems: sediment deposition, storm surges and vegetation. Wetlands 29, 24–34.CrossRefGoogle Scholar
Torrescano, N., and Islebe, G.A. (2006). Tropical forest and mangrove history from southeastern Mexico: a 5000 yr pollen record and implications for sea level rise. Vegetation History and Archaeobotany 15, 191–195.CrossRefGoogle Scholar
Urrego, L.E., Bernal, G., and Polanía, J. (2009). Comparison of pollen distribution patterns in surface sediments of a Colombian Caribbean mangrove with geomorphology and vegetation. Review of Palaeobotany and Palynology 156, 358–375.CrossRefGoogle Scholar
Van Campo, E., and Bengo, M.D. (2004). Mangrove palynology in recent marine sediments off Cameroon. Marine Geology 208, 315–330.CrossRefGoogle Scholar
van Soelen, E.E., Lammertsma, E.I., and Cremer, H. (2010). Late Holocene sea-level rise in Tampa Bay: integrated reconstruction using biomarkers, pollen, organic-walled dinoflagellate cysts, and diatoms. Estuarine, Coastal and Shelf Science 86, 216–224.CrossRefGoogle Scholar
van Soelen, E.E., Brooks, G.R., Larson, R.A., Damsté, J.S.S., and Reichart, G.J. (2012). Mid- to late-Holocene coastal environmental changes in southwest Florida, USA. The Holocene 1–10.Google Scholar
Versteegh, G.J.M., Schefuss, E., Dupont, L., Marret, F., Damste, J.S.S., and Jansen, J.H.F. (2004). Taraxerol and Rhizophora pollen as proxies for tracking past mangrove ecosystems. Geochimica et Cosmochimica Acta 68, 411–422.CrossRefGoogle Scholar
Wanless, H.R., Parkinson, R.W., and Tedesco, L.P. (1994). Sea level control on stability of Everglades wetlands. Davis, S.M., Ogden, J.C. Everglades: the ecosystem and its restoration St. Lucie Press, 199–222.Google Scholar
Whelan, K.R.T., Smith, T.J.I., Anderson, G.H., and Ouellette, M.L. (2009). Hurricane Wilma's impact on overall soil elevation and zones within the soil profile in a mangrove forest. Wetlands 29, 16–23.CrossRefGoogle Scholar
Willard, D.A., and Bernhardt, C.E. (2011). Impacts of past climate and sea level change on Everglades wetlands: placing a century of anthropogenic change into a late-Holocene context. Climatic Change 107, 59–80.CrossRefGoogle Scholar
Willard, D.A., and Cronin, T.M. (2007). Paleoecology and ecosystem restoration: case studies from Chesapeake Bay and the Florida Everglades. Frontiers in Ecology and the Environment 5, 491–498.CrossRefGoogle Scholar
Willard, D.A., Weimera, L.M., and Riegel, W.L. (2001). Pollen assemblages as paleoenvironmental proxies in the Florida Everglades. Review of Palaeobotany and Palynology 113, 213–235.CrossRefGoogle ScholarPubMed
Willard, D.A., Cooper, S.R., Gamez, D., and Jensen, J. (2004). Atlas of pollen and spores of the Florida Everglades. Palynology 28, 175–227.CrossRefGoogle Scholar
Woodroffe, C.D., Thom, B.G., and Chappell, J. (1985). Development of widespread mangrove swamps in mid-Holocene times in northern Australia. Nature 317, 711–713.CrossRefGoogle Scholar
Wooller, M.J., Behling, H., Smallwood, B.J., and Fogel, M. (2004). Mangrove ecosystem dynamics and elemental cycling at Twin Cays, Belize, during the Holocene. Journal of Quaternary Science 19, 703–711.CrossRefGoogle Scholar
Wooller, M.J., Morgan, R., Fowell, S., Behling, H., and Fogel, M. (2007). A multiproxy peat record of Holocene mangrove palaeoecology from Twin Cays, Belize. The Holocene 17, 8, 1129–1139.CrossRefGoogle Scholar
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