Abstract
This chapter focuses on the net primary productivity and carbon (C) dynamics of mangrove wetlands as related to the potential to sequester atmospheric C in above- and belowground biomass and in the soil. We discuss the large variation in ecosystem properties across different coastal environmental settings and pay particular attention to global patterns of these ecosystem processes comparing the Atlantic-East-Pacific and Indo-West-Pacific biogeographic regions. Deltaic coasts have higher aboveground biomass (AGB) compared to other continental settings, but the highest average AGB was found in high oceanic islands. The global average rates of litter fall (NPPL) and (NPPW) wood production are about 6 t ha−1 yr−1 for aboveground net primary productivity (NPPA) of about 12 t ha−1 yr−1. The relative contribution of belowground allocation to soil C storage and wood production to total net primary productivity (NPPT) in mangrove wetlands has significant implications to net C exchange in these coastal forested wetlands. Examples are given to demonstrate that net ecosystem production (NEP) and net ecosystem carbon exchange for mangrove wetlands have implications to the debate on how coastal ecosystems influence the global C budget. Wood production is about 600 g dry mass m−2 yr−1 or about 300 gC m−2 yr−1. The average C sequestration in mangroves soils (∆S org) is about 224 gC m−2 yr−1. The sum of these two measures (NPPW + ∆S org) is an estimate of NEP at about 525 gC m−2 yr−1. A general conclusion based on these different approaches, and reviewing the existing global literature, is that NEP accumulates about 500 gC m−2 yr−1, equally distributed between wood production and soil C accumulation. The importance of above and belowground contributions to global estimates of C sequestration above- and belowground reinforces the need for a better understanding of biomass allocation in these systems. The net tidal exchange of inorganic and organic carbon is about 400 gC m−2 yr−1 with nearly equal distribution in these forms of carbon to coastal waters. It is not clear how the fate of this material may influence net carbon exchange in the coastal zone, which is a very active area of research. We also suggest that more information is needed on how the disturbance of mangrove wetlands, including their recovery, may influence net carbon flux in the coastal zone.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Adame MF, Lovelock CE (2011) Carbon and nutrient exchange of mangrove forests with the coastal ocean. Hydrobiologia 663(1):23–50
Allen JA, Ewel KC, Keeland BD, Tara T, Smith TJ (2000) Downed wood in Micronesian mangrove forests. Wetlands 20(1):169–176
Allen MR, Barros VR, Broome J, Cramer W, Christ R, Church JA, Clarke L, Dahe Q, Dasgupta P, Dubash NK (2014) IPCC fifth assessment synthesis report-climate change 2014 synthesis report
Alongi D, Pfitzner J, Trott L, Tirendi F, Dixon P, Klumpp D (2005) Rapid sediment accumulation and microbial mineralization in forests of the mangrove Kandelia candel in the Jiulongjiang Estuary, China. Estuar Coast Shelf Sci 63(4):605–618
Alongi D, Wattayakorn G, Pfitzner J, Tirendi F, Zagorskis I, Brunskill G, Davidson A, Clough B (2001) Organic carbon accumulation and metabolic pathways in sediments of mangrove forests in southern Thailand. Mar Geol 179(1):85–103
Alongi DM (2002) Present state and future of the world’s mangrove forests. Environ Conserv 29(3):331–349
Alongi DM (2009) The energetics of mangrove forests. Springer, Dordrecht/London
Alongi DM (2011) Patterns of mangrove wood and litter production within a beach ridge-fringing reef embayment, northern great barrier reef coast. Estuar Coasts 34(1):32–44. doi:10.1007/s12237-010-9289-y
Alongi DM (2014) Carbon cycling and storage in mangrove forests. Annu Rev Mar Sci 6:195–219
Alongi DM, Boto KG, Tirendi F (1989) Effect of exported mangrove litter on bacterial productivity and dissolved organic carbon fluxes in adjacent tropical nearshore sediments. Mar Ecol Prog Ser 56:133–144
Alongi DM, Christoffersen P, Tirendi F (1993) The influence of forest type on microbial-nutrient relationships in tropical mangrove sediments. J Exp Mar Biol Ecol 171:201–223
Amarasinghe MD, Balasubramaniam S (1992) Net primary productivity of two mangrove forest stands on the northwestern coast of Sri Lanka. Hydrobiologia 247(1–3):37–47
Andersen FO, Kristensen E (1992) The importance of benthic macrofauna in decomposition of microalgae in a coastal marine sediment. Limnol Oceanogr 37(7):1392–1403
Araújo J Jr, Otero X, Marques A, Nóbrega G, Silva J, Ferreira T (2012) Selective geochemistry of iron in mangrove soils in a semiarid tropical climate: effects of the burrowing activity of the crabs Ucides cordatus and Uca maracoani. Geo-Mar Lett 32(4):289–300
Armentano T, Menges E (1986) Patterns of change in the carbon balance of organic soil-wetlands of the temperate zone. J Ecol 74:755–774
Baldocchi D (2008) ‘Breathing’ of the terrestrial biosphere: lessons learned from a global network of carbon dioxide flux measurement systems. Aust J Bot 56(1):1–26. doi:http://dx.doi.org/10.1071/BT07151
Baldocchi DD (2003) Assessing the eddy covariance technique for evaluating carbon dioxide exchange rates of ecosystems: past, present and future. Glob Chang Biol 9(4):479–492
Barr JG, Engel V, Fuentes JD, Zieman JC, O’Halloran TL, Smith TJ, Anderson GH (2010) Controls on mangrove forest-atmosphere carbon dioxide exchanges in western Everglades National Park. J Geophys Res Biogeo 115, G02020, doi:10.1029/2009JG001186
Borges AV, Djenidi S, Lacroix G, Theate J, Delille B, Frankignoulle M (2003) Atmospheric CO2 flux from mangrove surrounding waters. Geophys Res Lett 30(11):12-11–12-14
Bosire JO, Dahdouh-Guebas F, Kairo JG, Wartel S, Kazungu J, Koedam N (2006) Success rates of recruited tree species and their contribution to the structural development of reforested mangrove stands. Mar Ecol Prog Ser 325:85–91. doi:10.3354/meps325085
Bosire JO, Dahdouh-Guebas F, Kairo JG, ZKazungu J, Dehairs F, Koedam N (2005) Litter degradation and CN dynamics in reforested mangrove plantations at Gazi Bay, Kenya. Biol Conserv 126:287–295
Boto KG, Bunt JS (1981) Tidal export of particulate organic matter from a northern Australian mangrove system. Estuar Coast Shelf Sci 13:247–255
Boto KG, Wellington JT (1988) Seasonal variations in concentrations and fluxes of dissolved organic and inorganic materials in a tropical, tidally-dominated, mangrove waterway. Mar Ecol Prog Ser 50:151–160
Bouillon S, Borges AV, Castaneda-Moya E, Diele K, Dittmar T, Duke NC, Kristensen E, Lee SY, Marchand C, Middelburg JJ, Rivera-Monroy VH, Smith TJ, Twilley RR (2008) Mangrove production and carbon sinks: a revision of global budget estimates. Glob Biogeochem Cycles 22(2). doi:10.1029/2007gb003052
Bouillon S, Koedam N, Baeyens W, Satyanarayana B, Dehairs F (2004a) Selectivity of subtidal benthis invertebrate communities for local microalgal production in an estuarine mangrove ecosystem during the post-monsoon period. J Sea Res 51(2):133–144
Bouillon S, Koedam N, Raman AV, Dehairs F (2002a) Primary producers sustaining macro-invertebrate communities in intertidal mangrove forests. Oecologia 130:441–448
Bouillon S, Middelburg JJ, Dehairs F, Borges AV, Abril G, Flindt MR, Ulomi S, Kristensen E (2007) Importance of intertidal sediment processes and porewater exchange on the water column biogeochemistry in a pristine mangrove creek (Ras Dege, Tanzania). Biogeosci Discuss 4(1):317–348
Bouillon S, Moens T, Overmeer I, Koedam N, Dehairs F (2004b) Resource utilization patterns of epifauna from mangrove forests with contrasting inputs of local versus imported organic matter. Mar Ecol Prog Ser 278:77–88
Bouillon S, Raman A, Dauby P, Dehairs F (2002b) Carbon and nitrogen stable isotope ratios of subtidal benthic invertebrates in an estuarine mangrove ecosystem (Andhra Pradesh, India). Estuar Coast Shelf Sci 54(5):901–913
Breithaupt JL, Smoak JM, Smith TJ, Sanders CJ, Hoare A (2012) Organic carbon burial rates in mangrove sediments: strengthening the global budget. Glob Biogeochem Cycles 26, GB3011, doi:10.1029/2012GB004375
Brown S, Lugo AE (1984) Biomass of tropical forests: a new estimate based on forest volumes. Science 223:1290–1293
Bulmer RH, Lundquist C, Schwendenmann L (2015) Sediment properties and CO2 efflux from intact and cleared temperate mangrove forests. Biogeosciences 12(20):6169–6180
Cahoon DR, Hensel P, Rybczyk J, McKee KL, Proffitt CE, Perez BC (2003) Mass tree mortality leads to mangrove peat collapse at Bay Islands, Honduras after Hurricane Mitch. J Ecol 91(6):1093–1105. doi:10.1046/j.1365-2745.2003.00841.x
Cai W-J (2011) Estuarine and coastal ocean carbon paradox: CO2 sinks or sites of terrestrial carbon incineration? Annu Rev Mar Sci 3:123–145
Caldeira K (2012) Avoiding mangrove destruction by avoiding carbon dioxide emissions. Proc Natl Acad Sci 109(36):14287–14288
Call M, Maher DT, Santos IR, Ruiz-Halpern S, Mangion P, Sanders CJ, Erler DV, Oakes JM, Rosentreter J, Murray R (2015) Spatial and temporal variability of carbon dioxide and methane fluxes over semi-diurnal and spring–neap–spring timescales in a mangrove creek. Geochim Cosmochim Acta 150:211–225
Canadell JG, Raupach MR (2008) Managing forests for climate change mitigation. Science 320(5882):1456–1457
Cannicci S, Burrows D, Fratini S, Smith TJ, Offenberg J, Dahdouh-Guebas F (2008) Faunal impact on vegetation structure and ecosystem function in mangrove forests: a review. Aquat Bot 89(2):186–200
Castañeda-Moya E, Rivera-Monroy VH, Twilley RR (2006) Mangrove zonation in the dry life zone of the Gulf of Fonseca, Honduras. Estuar Coasts 29(5):751–764
Castañeda-Moya E, Twilley RR, Rivera-Monroy VH (2013) Allocation of biomass and net primary productivity of mangrove forests along environmental gradients in the Florida Coastal Everglades, USA. For Ecol Manag 307:226–241
Castañeda-Moya E, Twilley RR, Rivera-Monroy VH, Marx BD, Coronado-Molina C, Ewe SML (2011) Patterns of root dynamics in mangrove forests along environmental gradients in the Florida Coastal Everglades, USA. Ecosystems 14(7):1178–1195. doi:10.1007/s10021-011-9473-3
Castañeda-Moya E, Twilley RR, Rivera-Monroy VH, Zhang KQ, Davis SE, Ross M (2010) Sediment and nutrient deposition associated with Hurricane Wilma in mangroves of the Florida Coastal Everglades. Estuar Coasts 33(1):45–58. doi:10.1007/S12237-009-9242-0
Chalermchatwilai B, Poungparn S, Patanaponpaiboon P (2011) Distribution of fine-root necromass in a secondary mangrove forest in Trat province, Eastern Thailand. ScienceAsia 37:1–5
Chapin FS III, Woodwell GM, Randerson JT, Rastetter EB, Lovett GM, Baldocchi DD, Clark DA, Harmon ME, Schimel DS, Valentini R (2006) Reconciling carbon-cycle concepts, terminology, and methods. Ecosystems 9(7):1041–1050
Chen L, Zan Q, Li M, Shen J, Liao W (2009) Litter dynamics and forest structure of the introduced Sonneratia caseolaris mangrove forest in Shenzhen, China. Estuar Coast Shelf Sci 85(2):241–246. doi:http://dx.doi.org/10.1016/j.ecss.2009.08.007
Chen R, Twilley RR (1999) A simulation model of organic matter and nutrient accumulation in mangrove wetland soils. Biogeochemistry 44:93–118
Chmura GL, Anisfeld SC, Cahoon DR, Lynch JC (2003) Global carbon sequestration in tidal, saline wetland soils. Glob Biogeochem Cycles 17(4):12. doi:10.1029/2002gb001917
Christensen B (1978) Biomass and primary production of Rhizophora apiculata Bl. in a mangrove in southern Thailand. Aquat Bot 4:43–52. doi:http://dx.doi.org/10.1016/0304-3770(78)90005-0
Cifuentes LA, Coffin RB, Solorzano L, Cardenas W, Espinoza J, Twilley RR (1996) Isotopic and elemental variations of carbon and nitrogen in a mangrove estuary. Estuar Coast Shelf Sci 43(6):781–800
Cintrón G, Schaeffer-Novelli Y (1984) Caracteristicas y desarrollo estructural de los manglares de Norte y Sur America. Cienc Interam 25(1–4):4–15
Clark DA, Brown S, Kicklighter DW, Chambers JQ, Thomlinson JR, Ni J (2001) Measuring net primary production in forests: concepts and field methods. Ecol Appl 11(2):356–370
Cole TG, Ewel KC, Devoe NN (1999) Structure of mangrove trees and forests in Micronesia. For Ecol Manag 117(1–3):95–109. doi:http://dx.doi.org/10.1016/S0378-1127(98)00474-5
Comeaux RS, Allison MA, Bianchi TS (2012) 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. doi:10.1016/j.ecss.2011.10.003
Cormier N, Twilley RR, Ewel KC, Krauss KW (2015) Fine root productivity varies along nitrogen and phosphorus gradients in high-rainfall mangrove forests of Micronesia. Hydrobiologia 750(1):69–87
Coronado-Molina C, Alvarez-Guillen H, Day JW Jr, Reyes E, Perez BC, Vera-Herrera F, Twilley R (2012) Litterfall dynamics in carbonate and deltaic mangrove ecosystems in the Gulf of Mexico. Wetl Ecol Manag 20(2):123–136. doi:10.1007/s11273-012-9249-3
Crase B, Liedloff A, Vesk PA, Burgman MA, Wintle BA (2013) Hydroperiod is the main driver of the spatial pattern of dominance in mangrove communities. Glob Ecol Biogeogr 22(7):806–817. doi:10.1111/geb.12063
Cuevas E, Medina E (1988) Nutrient dynamics within amazonian forests II. Fine root growth, nutrient availability and leaf litter decomposition. Oecologia 76:222–235
Danielson TM (2016) Everglades mangrove forest response to large-scale disturbance: long-term assessment of structural and functional properties. Louisiana State University, Baton Rouge
Davis SE, Childers DL, Day JW, Rudnick DT, Sklar FH (2001) Wetland-water column exchanges of carbon, nitrogen, and phosphorus in a southern Everglades dwarf mangrove. Estuaries 24(4):610–622
Day JW, Conner WH, Ley-Lou F, Day RH, Navarro AM (1987) The productivity and composition of mangrove forests, Laguna de Terminos, Mexico. Aquat Bot 27:267–284
Day JW, Coronado-Molina C, Vera-Herrera FR, Twilley RR, Rivera-Monroy VH, Alvarez-Guillen H, Day R, Conner W (1996) A 7 year record of above-ground net primary production in a southeastern Mexican mangrove forest. Aquat Bot 55(1):39–60
Dittmar T, Hertkorn N, Kattner G, Lara RJ (2006) Mangroves, a major source of dissolved organic carbon to the oceans. Glob Biogeochem Cycles 20, GB1012, doi:10.1029/2005GB002570
Dittmar T, Lara RJ (2001) Do mangroves rather than rivers provide nutrients to coastal environments south of the Amazon River? Evidence from long-term flux measurements. Mar Ecol Prog Ser 213:67–77
Donato DC, Kauffman JB, Murdiyarso D, Kurnianto S, Stidham M, Kanninen M (2011) Mangroves among the most carbon-rich forests in the tropics. Nat Geosci 4(5):293–297. doi:http://www.nature.com/ngeo/journal/v4/n5/abs/ngeo1123.html - supplementary-information
Doughty CL, Langley JA, Walker WS, Feller IC, Schaub R, Chapman SK (2016) Mangrove range expansion rapidly increases coastal wetland carbon storage. Estuar Coasts 39(2):385–396
Duarte CM, Cebrian J (1996) The fate of marine autotrophic production. Limnol Oceanogr 41(8):1758–1766
Duarte CM, Middelburg JJ, Caraco N (2005) Major role of marine vegetation on the oceanic carbon cycle. Biogeosciences 2(1):1–8
Ellison AM (2002) Macroecology of mangroves: large-scale patterns and processes in tropical coastal forests. Trees-Struct Funct 16(2–3):181–194. doi:10.1007/s00468-001-0133-7
Ewe SML, Gaiser EE, Childers DL, Iwaniec D, Rivera-Monroy VH, Twilley RR (2006) Spatial and temporal patterns of aboveground net primary productivity (ANPP) along two freshwater-estuarine transects in the Florida Coastal Everglades. Hydrobiologia 569:459–474. doi:10.1007/S10750-006-0149-5
Ewel KC, Twilley RR, Eong-Ong J (1998) Different kinds of mangrove forests provide different goods and services. Glob Ecol Biogeogr 7:83–94
Feller IC (1995) Effects of nutrient enrichment on growth and herbivory of dwarf red mangrove (Rhizophora mangle). Ecol Monogr 65(4):477–505
Feller IC, Lovelock C, Berger U, McKee K, Joye S, Ball M (2010) Biocomplexity in mangrove ecosystems. Annu Rev Mar Sci 2:395–417
Feller IC, Lovelock C, McKee KL (2007) Nutrient addition differentially affects ecological processes of Avicennia germinans in nitrogen versus phosphorus limited mangrove ecosystems. Ecosystems 10(3):347–359
Ferreira T, Otero X, Vidal-Torrado P, Macías F (2007) Effects of bioturbation by root and crab activity on iron and sulfur biogeochemistry in mangrove substrate. Geoderma 142(1):36–46
Fleming M, Lin G, Sternberg LSL (1990) Influence of mangrove detritus in an estuarine ecosystem. Bull Mar Sci 47:663–669
Fontalvo-Herazo ML, Piou C, Vogt J, Saint-Paul U, Berger U (2011) Simulating harvesting scenarios towards the sustainable use of mangrove forest plantations. Wetl Ecol Manag 19(5):397–407. doi:10.1007/s11273-011-9224-4
Friess DA, Webb EL (2014) Variability in mangrove change estimates and implications for the assessment of ecosystem service provision. Glob Ecol Biogeogr 23(7):715–725
Fry B, Smith TJ (2002) Stable isotope studies of red mangroves and filter feeders from the Shark River estuary, Florida. Bull Mar Sci 70(3):871–890
Ganguly D, Dey M, Mandal S, De T, Jana T (2008) Energy dynamics and its implication to biosphere–atmosphere exchange of CO2, H2O and CH 4 in a tropical mangrove forest canopy. Atmos Environ 42(18):4172–4184
Gedan KB, Kirwan ML, Wolanski E, Barbier EB, Silliman BR (2011) The present and future role of coastal wetland vegetation in protecting shorelines: answering recent challenges to the paradigm. Clim Chang 106(1):7–29. doi:10.1007/s10584-010-0003-7
Giri C, Ochieng E, Tieszen LL, Zhu Z, Singh A, Loveland T, Masek J, Duke N (2011) Status and distribution of mangrove forests of the world using earth observation satellite data. Glob Ecol Biogeogr 20(1):154–159
Giri C, Zhu Z, Tieszen L, Singh A, Gillette S, Kelmelis J (2008) Mangrove forest distributions and dynamics (1975–2005) of the tsunami-affected region of Asia. J Biogeogr 35(3):519–528
Gleason S, Ewel KC (2002) Organic matter dynamics on the forest floor of a Micronesian mangrove forest: an investigation of speices composition shifts. Biotropica 34(2):190–198
Golley FB, Odum HT, Wilson RF (1962) The structure and metabolism of a Puerto Rican red mangrove forest in May. Ecology 43:9–19
Gong W-K, Ong J-E (1990) Plant biomass and nutrient flux in a managed mangrove forest in Malaysia. Estuar Coast Shelf Sci 31(5):519–530. doi:http://dx.doi.org/10.1016/0272-7714(90)90010-O
Graham SA, Mendelssohn IA (2016) Contrasting effects of nutrient enrichment on below-ground biomass in coastal wetlands. J Ecol 104(1):249–260
Granek EF, Compton JE, Phillips DL (2009) Mangrove-exported nutrient incorporation by sessile coral reef invertebrates. Ecosystems 12(3):462–472
Heald EJ (1969) The production of organic detritus in a south Florida estuary. Ph.D. Disseration, University of Miami, Coral Gables, Florida
Hemminga MA, Slim FJ, Kazungu J, Ganssen GM, Nieuwenhuize J, Kruyt NM (1994) Carbon outwelling from a mangrove forest with adjacent seagrass beds and coral reefs (Gazi Bay, Kenya). Mar Ecol Prog Ser 106:291–301
Hopkinson CS, Cai WJ, Hu XP (2012) Carbon sequestration in wetland dominated coastal systems – a global sink of rapidly diminishing magnitude. Curr Opin Environ Sustain 4(2):186–194. doi:10.1016/j.cosust.2012.03.005
Houghton R (2007) Balancing the global carbon budget. Annu Rev Earth Planet Sci 35:313–347
Houghton RA (1994) The worldwide extent of land-use change. Bioscience 44(5):305–313
Hutchison J, Manica A, Swetnam R, Balmford A, Spalding M (2013) Predicting global patterns in mangrove forest biomass. Conserv Lett 7(3):233–240
Jackson RB, Mooney H, Schulze E-D (1997) A global budget for fine root biomass, surface area, and nutrient contents. Proc Natl Acad Sci 94(14):7362–7366
Jaffe R, Boyer JN, Lu X, Maie N, Yang C, Scully NM, Mock S (2004) Source characterization of dissolved organic matter in a subtropical mangrove-dominated estuary by fluorescence analysis. Mar Chem 84(3–4):195–210
Jaffe R, Mead R, Hernandez ME, Peralba MC, DiGuida OA (2001) Origin and transport of sedimentary organic matter in two subtropical estuaries: a comparative, biomarker-based study. Org Geochem 32(4):507–526
Jardine SL, Siikamäki JV (2014) A global predictive model of carbon in mangrove soils. Environ Res Lett 9(10):104013
Jennerjahn TC, Ittekkot V (2002) Relevance of mangroves for the production and deposition of organic matter along tropical continental margins. Naturwissenschaften 89(1):23–30
Jin-Eong O, Khoon GW, Clough BF (1995) Structure and productivity of a 20-year-old stand of Rhizophora apiculata Bl. mangrove forest. J Biogeogr 22(2/3):417–424. doi:10.2307/2845938
Junk W, Piedade M, Lourival R, Wittmann F, Kandus P, Lacerda L, Bozelli R, Esteves F, Nunes da Cunha C, Maltchik L (2014) Brazilian wetlands: their definition, delineation, and classification for research, sustainable management, and protection. Aquat Conserv Mar Freshwat Ecosyst 24(1):5–22
Kairo J, Bosire J, Langat J, Kirui B, Koedam N (2009) Allometry and biomass distribution in replanted mangrove plantations at Gazi Bay, Kenya. Aquat Conserv Mar Freshwat Ecosyst 19(S1):S63–S69
Kairo JG, Lang’at JKS, Dahdouh-Guebas F, Bosire J, Karachi M (2008) Structural development and productivity of replanted mangrove plantations in Kenya. For Ecol Manag 255(7):2670–2677. doi:http://dx.doi.org/10.1016/j.foreco.2008.01.031
Kauffman JB, Heider C, Cole TG, Dwire KA, Donato DC (2011) Ecosystem carbon stocks of Micronesian mangrove forests. Wetlands 31(2):343–352
Khan MNI, Suwa R, Hagihara A (2009) Biomass and aboveground net primary production in a subtropical mangrove stand of Kandelia obovata (S., L.) Yong at Manko Wetland, Okinawa, Japan. Wetl Ecol Manag 17(6):585–599
Khan NI, Suwa R, Hagihara A (2007) Carbon and nitrogen pools in a mangrove stand of Kandelia obovata (S., L.) Yong: vertical distribution in the soil-vegetation system. Wetl Ecol Manag 15:141–153
Kirwan M, Temmerman S (2009) Coastal marsh response to historical and future sea-level acceleration. Quat Sci Rev 28(17):1801–1808. doi:http://dx.doi.org/10.1016/j.quascirev.2009.02.022
Kirwan ML, Guntenspergen GR (2012) Feedbacks between inundation, root production, and shoot growth in a rapidly submerging brackish marsh. J Ecol 100(3):764–770. doi:10.1111/j.1365-2745.2012.01957.x
Kirwan ML, Guntenspergen GR, D’Alpaos A, Morris JT, Mudd SM, Temmerman S (2010) Limits on the adaptability of coastal marshes to rising sea level. Geophys Res Lett 37. doi:10.1029/2010gl045489
Kirwan ML, Mudd SM (2012) Response of salt-marsh carbon accumulation to climate change. Nature 489(7417):550. doi:10.1038/nature11440
Komiyama A, Ogino K, Aksornkoae S, Sabhasri S (1987) Root biomass of a mangrove forest in southern Thailand,. 1. Estimation by the trench method and the zonal structure of root biomass. J Trop Ecol 3:97–108
Komiyama A, Ong JE, Poungparn S (2008) Allometry, biomass, and productivity of mangrove forests: a review. Aquat Bot 89(2):128–137
Koné Y-M, Borges A (2008) Dissolved inorganic carbon dynamics in the waters surrounding forested mangroves of the Ca Mau Province (Vietnam). Estuar Coast Shelf Sci 77(3):409–421
Krauss KW, Doyle TW, Twilley RR, Rivera-Monroy VH, Sullivan JK (2006) Evaluating the relative contributions of hydroperiod and soil fertility on growth of south Florida mangroves. Hydrobiologia 569:311–324. doi:10.1007/S10750-006-0139-7
Krauss KW, Doyle TW, Twilley RR, Smith TJ, Whelan KRT, Sullivan JK (2005) Woody debris in the mangrove forests of South Florida. Biotropica 37(1):9–15
Krauss KW, Lovelock CE, McKee KL, López-Hoffman L, Ewe SM, Sousa WP (2008) Environmental drivers in mangrove establishment and early development: a review. Aquat Bot 89(2):105–127
Kreuzwieser J, Buchholz J, Rennenberg H (2003) Emission of methane and nitrous oxide by Australian mangrove ecosystems. Plant Biol 5(04):423–431
Kristensen E (1988) Benthic fauna and biogeochemical processes in marine sediments. II. Microbial activities and fluxes. In: Blackburn TH, Sørensen J (eds) Nitrogen cycling in coastal marine environments. Wiley, Chichester, pp 275–299
Kristensen E (2007) Carbon balance in mangrove sediments: the driving processes and their controls. In: Greenhouse gas and carbon balances in mangrove coastal ecosystems. Gendai Tosho, Tokyo, pp 61–78
Kristensen E (2008) Mangrove crabs as ecosystem engineers; with emphasis on sediment processes. J Sea Res 59(1):30–43
Kristensen E, Alongi DM (2006) Control by fiddler crabs (Uca vocas) and plant roots (Avicennia marina) on carbon, iron, and sulfur biogeochemistry in mangrove sediment. Limnol Oceanogr 51(4):1557–1571
Kristensen E, Andersen FØ, Holmboe N, Holmer M, Thongtham N (2000) Carbon and nitrogen mineralization in sediments of the Bangrong mangrove area, Phuket, Thailand. Aquat Microb Ecol 22(2):199–213
Kristensen E, Bouillon S, Dittmar T, Marchand C (2008) Organic carbon dynamics in mangrove ecosystems: a review. Aquat Bot 89(2):201–219
Kristensen E, Mangion P, Tang M, Flindt MR, Holmer M, Ulomi S (2011) Microbial carbon oxidation rates and pathways in sediments of two Tanzanian mangrove forests. Biogeochemistry 103(1–3):143–158
Kuenzer C, Bluemel A, Gebhardt S, Quoc TV, Dech S (2011) Remote sensing of mangrove ecosystems: a review. Remote Sens 3(5):878–928
Lee S (1995) Mangrove outwelling: a review. Hydrobiologia 295(1–3):203–212
Lee S (1997) Potential trophic importance of the faecal material of the mangrove sesarmine crab Sesarma messa. Mar Ecol Prog Ser 159:275–284
Lee SY (1989a) The importance of sesarminae crabs Chiromanthes spp. and inundation frequency on mangrove (Kandelia candel (L.) Druce) leaf litter turnover in a Hong Kong tidal shrimp pond. J Exp Mar Biol Ecol 131:23–43
Lee SY (1989b) Litter production and turnover of the mangrove Kandelia candel (L.) Druce in a Hong Kong tidal shrimp pond. Estuar Coast Shelf Sci 29:75–87
Lee SY (1990) Primary productivity and particulate organic matter flow in an estuarine mangrove-wetland in Hong Kong. Mar Biol 106:453–463
Lee SY (2004) Relationship between mangrove abundance and tropical prawn production: a re-evaluation. Mar Biol 145(5):943–949
Lee SY (2005) Exchange of organic matter and nutrients between mangroves and estuaries: myths, methodological issues and missing links. Int J Ecol Environ Sci 31(3):163–176
Lee SY (2008) Mangrove macrobenthos: assemblages, services, and linkages. J Sea Res 59(1):16–29
Leopold A, Marchand C, Deborde J, Allenbach M (2015) Temporal variability of CO2 fluxes at the sediment-air interface in mangroves (New Caledonia). Sci Total Environ 502:617–626
Leopold A, Marchand C, Deborde J, Chaduteau C, Allenbach M (2013) Influence of mangrove zonation on CO2 fluxes at the sediment–air interface (New Caledonia). Geoderma 202:62–70
Li X, Zhu J, Lange H, Han S (2012) A modified ingrowth core method for measuring fine root production, mortality and decomposition in forests. Tree Physiol 33(1):18–25
Linto N, Barnes J, Ramachandran R, Divia J, Ramachandran P, Upstill-Goddard R (2014) Carbon dioxide and methane emissions from mangrove-associated waters of the Andaman Islands, Bay of Bengal. Estuar Coasts 37(2):381–398
Lopez-Hoffman L, Anten NP, Martinez-Ramos M, Ackerly DD (2007) Salinity and light interactively affect neotropical mangrove seedlings at the leaf and whole plant levels. Oecologia 150(4):545–556
Lovelock C, Feller IC, Ball M, Engelbrecht B, Ewe ML (2006) Difference in plant function in phosphorous- and nitrgoen- limited mangrove ecosystems. New Phytol 172:514–522
Lovelock C, Feller IC, McKee KL, Engelbrecht B, Ball M (2004) The effect of nutrient enrichment on growth, photosynthesis and hydraulic conductance of dwarf mangroves in Panama. Funct Ecol 18(1):25–33
Lovelock CE (2008) Soil respiration and belowground carbon allocation in mangrove forests. Ecosystems 11(2):342–354
Lovelock CE, Feller IC, Ellis J, Schwarz AM, Hancock N, Nichols P, Sorrell B (2007) Mangrove growth in New Zealand estuaries: the role of nutrient enrichment at sites with contrasting rates of sedimentation. Oecologia 153(3):633–641
Ludovici KH, Zarnoch SJ, Richter DD (2002) Modeling in-situ pine root decomposition using data from a 60-year chronosequence. Can J For Res 32(9):1675–1684
Lugo AE (1990) Fringe wetlands. In: Lugo AE, Brinson M, Brown S (eds) Forested wetlands, Ecosystems of the world, vol 15. Elsevier, Amsterdam, pp 143–169
Lugo AE (1997) Old-growth mangrove forests in the United States. Conserv Biol 11(1):11–20. doi:10.2307/2387271
Lugo AE, Brown S, Brinson MM (1988) Forested wetlands in freshwater and salt-water environments. Limnol Oceanogr 33(4):894–909. doi:10.2307/2837228
Lugo AE, Snedaker SC (1974) The ecology of mangroves. Ann Rev Ecol Syst 5:39–64
Lynch JC, Meriwether JR, McKee BA, Vera-Herrera F, Twilley RR (1989) Recent accretion in mangrove ecosystems based on 137Cs and 210Pb. Estuaries 12:284–299
Machiwa JF (1999) Lateral fluxes of organic carbon in a mangrove forest partly contaminated with sewage wastes. Mangrove Salt Marshes 3(2):95–104
Macnae W (1974) Mangrove forests and fisheries. Food and Agriculture Organization of the United Nations/United Nations Development Programme, Rome
Maher DT, Santos IR, Golsby-Smith L, Gleeson J, Eyre BD (2013) Groundwater-derived dissolved inorganic and organic carbon exports from a mangrove tidal creek: the missing mangrove carbon sink? Limnol Oceanogr 58(2):475–488
Maie N, Pisani O, Jaffe R (2008) Mangrove tannins in aquatic ecosystems: their fate and possible influence on dissolved organic carbon and nitrogen cycling. Limnol Oceanogr 53(1):160–171
Majdi H, Kangas P (1997) Demography of fine roots in response to nutrient applications in a Norway spruce stand in southwestern Sweden. Ecoscience 4(2):199–205
McKee KL (2011) Biophysical controls on accretion and elevation change in Caribbean mangrove ecosystems. Estuar Coast Shelf Sci 91(4):475–483
McKee KL, Cahoon DR, Feller IC (2007) Caribbean mangroves adjust to rising sea level through biotic controls on change in soil elevation. Glob Ecol Biogeogr 16(5):545–556. doi:10.1111/j.1466-8238.2007.00317.x
McKee KL, Faulkner PL (2000) Restoration of biogeochemical function in mangrove forests. Restor Ecol 8(3):247–259
Mcleod E, Chmura GL, Bouillon S, Salm R, Björk M, Duarte CM, Lovelock CE, Schlesinger WH, Silliman BR (2011) A blueprint for blue carbon: toward an improved understanding of the role of vegetated coastal habitats in sequestering CO2. Front Ecol Environ 9(10):552–560
Mfilinge PL, Atta N, Tsuchiya M (2002) Nutrient dynamics and leaf litter decomposition in a subtropical mangrove forest at Oura Bay, Okinawa, Japan. Trees 16:172–180
Mfilinge PL, Meziane T, Bachok Z, Tsuchiya M (2005) Litter dynamics and particulate organic matter outwelling from a subtropical mangrove in Okinawa Island, South Japan. Estuar Coast Shelf Sci 63(1–2):301–313. doi:http://dx.doi.org/10.1016/j.ecss.2004.11.022
Middleton BA, McKee KL (2001) Degradation of mangrove tissues and implications for peat formation in Belizean island forests. J Ecol 89:818–828
Moncrieff JB, Jarvis PG, Valentini R (2000) Canopy fluxes. In: Methods in ecosystem science. Springer, New York/London, pp 161–180
Nadelhoffer KJ, Aber JD, Melillo JM (1985) Fine roots, net primary production, and soil nitrogen availability: a new hypothesis. Ecology 66(4):1377–1390
Nadelhoffer KJ, Raich JW (1992) Fine root production estimates and belowground carbon allocation in forest ecosystems. Ecology 73(4):1139–1147
Naidoo G (2009) Differential effects of nitrogen and phosphorus enrichment on growth of dwarf Avicennia marina mangroves. Aquat Bot 90(2):184–190
Nielsen OI, Kristensen E, Macintosh DJ (2003) Impact of fiddler crabs (Uca spp.) on rates and pathways of benthic mineralization in deposited mangrove shrimp pond waste. J Exp Mar Biol Ecol 289(1):59–81
Nixon SW (1980) Between coastal marshes and coastal waters-a review of twenty years of speculation and research on the role of salt marshes in estuarine productivity and water chemistry. In: Hamilton P, MacDonald KB (eds) Estuarine and wetland processes with emphasis on modeling. Plenum, New York, pp 437–525
Odum EP (2002) Tidal marshes as outwelling/pulsing systems. In: Concepts and controversies in tidal marsh ecology. Dordrecht, pp 3–7
Odum WE (1984) Dual-gradient concept of detritus transport and processing in estuaries. Bull Mar Sci 35(3):510–521
Odum WE, Heald EJ (1972) Trophic analyses of an estuarine mangrove community. Bull Mar Sci 22:671–738
Odum WE, Heald EJ (1975) The detritus-based food web of an estuarine mangrove community. In: Cronin LE (ed) Estuarine research. Academic, New York, pp 265–286
Ólafsson E, Buchmayer S, Skov MW (2002) The East African decapod crab Neosarmatium meinerti (de Man) sweeps mangrove floors clean of leaf litter. AMBIO J Hum Environ 31(7):569–573
Olafsson E, Ndaro S (1998) Impact of the mangrove crabs Uca annulipes and Dotilla fenestrata on meiobenthos. Oceanogr Lit Rev 6(45):1004–1005
Ong JE, Khoon GW, Hoong WC, Dhanarajan G (1979) Productivity of a managed mangrove forest in west Malaysia. In: Noor, YM (ed) Trends in applied biology in southeast Asia. University Sains Press, Penang, pp 1–10
Osland MJ, Enwright N, Day RH, Doyle TW (2013) Winter climate change and coastal wetland foundation species: salt marshes vs. mangrove forests in the southeastern United States. Glob Chang Biol 19(5):1482–1494
Parkinson RW, DeLaune RD, White JR (1994) Holocene sea-level rise and the fate of mangrove forests within the wider caribbean region. J Coast Res 10(4):1077–1086
Peckarsky BL (1980) Influence of detritus upon colonization of stream invertebrates. Can J Fish Aquat Sci 37(6):957–963
Penha-Lopes G, Kristensen E, Flindt M, Mangion P, Bouillon S, Paula J (2010) The role of biogenic structures on the biogeochemical functioning of mangrove constructed wetlands sediments–a mesocosm approach. Mar Pollut Bull 60(4):560–572
Pineda JEM (2003) The contribution of mangrove outwelling to coastal food webs as a function of environmental settings. University of Louisiana at Lafayette, Lafayette
Pool DJ, Lugo AE, Snedaker SC (1975) Litter production in mangrove forests of southern Florida and Puerto Rico. In: Walsh GE, Snedaker SC, Teas HJ (eds) Proceedings of the international symposium on biology and management of mangroves. East-West Center, Honolulu, pp 213–237
Poret N, Twilley RR, Rivera-Monroy VH, Coronado-Molina C (2007) Belowground decomposition of mangrove roots in Florida Coastal Everglades. Estuar Coasts 30(3):491–496
Primavera JH (1996) Stable carbon and nitrogen isotope ratios of Penaeid juveniles and primary producers in a reverine mangrove in Guimaras, Philippines. Bull Mar Sci 58:675–683
Purvaja R, Ramesh R (2001) Natural and anthropogenic methane emission from coastal wetlands of South India. Environ Manag 27(4):547–557
Putz FE, Chan HT (1986) Tree growth, dynamics, and productivity in a mature mangrove forest in Malaysia. For Ecol Manag 17:211–230
Reef R, Feller IC, Lovelock CE (2010) Nutrition of mangroves. Tree Physiol 30(9):1148–1160
Ren H, Jian S, Lu H, Zhang Q, Shen W, Han W, Yin Z, Guo Q (2008) Restoration of mangrove plantations and colonisation by native species in Leizhou bay, South China. Ecol Res 23(2):401–407. doi:10.1007/s11284-007-0393-9
Rivera-Monroy, VH, Castañeda-Moya E, Barr JG, Engel V, Fuentes JD, Troxler TG, Twilley RR, Bouillon S, Smith TJ, O’Halloran TL (2013). Current Methods to Evaluate Net Primary Production and Carbon Budgets in Mangrove Forests. In: DeLaune RD, Reddy KR, Richardson CJ, Megonigal JP (eds) Methods in Biogeochemistry of Wetlands, SSSA Book Ser. 10. SSSA, Madison, WI, pp 243–288. doi:10.2136/sssabookser10.c14
Robertson A, Alongi D (1995) Role of riverine mangrove forests in organic carbon export to the tropical coastal ocean: a preliminary mass balance for the Fly Delta (Papua New Guinea). Geo-Mar Lett 15(3–4):134–139
Robertson A, Alongi D, Boto K (1993) Food chains and carbon fluxes. In: Alongi DM, Robertson AI (eds) Tropical mangrove ecosystems. American Geophysical Union, Washington, D. C, pp 293–326. doi:10.1029/CE041p0293
Robertson AI (1986) Leaf-burying crabs: their influence on energy flow and export from mixed mangrove forests (Rhizophora spp) in northeastern Australia. J Exp Mar Biol Ecol 102:237–248
Rodelli MR, Gearing JN, Gearing PJ, Marshall N, Sasekumar A (1984) Stable isotope ratio as a tracer of mangrove carbon in Malaysian ecosystems. Oecologia 61:326–333
Romigh MM, Davis SE, Rivera-Monroy VH, Twilley RR (2006) Flux of organic carbon in a riverine mangrove wetland in the Florida Coastal Everglades. Hydrobiologia 569:505–516. doi:10.1007/S10750-006-0152-X
Ross MS, Meeder JF, Sah JP, Ruiz PL, Telesnicki GJ (2000) The southeast saline everglades revisited: 50 years of coastal vegetation change. J Veg Sci 11:101–112
Ross MS, Ruiz PL, Telesnicki GJ, Meeder JF (2001) Estimating above-ground biomass and production in mangrove communities of Biscayne National Park, Florida (USA). Wetl Ecol Manag 9(1):27–37
Rovai A, Riul P, Twilley R, Castañeda-Moya E, Rivera-Monroy V, Williams A, Simard M, Cifuentes-Jara M, Lewis R, Crooks S (2016) Scaling mangrove aboveground biomass from site-level to continental-scale. Glob Ecol Biogeogr 25(3):286–298
Saenger P, Snedaker SC (1993) Pantropical trends in mangroves above-ground biomass and annual litterfall. Oecologia 96:293–299
Saintilan N (2004) Relationships between estuarine geomorphology, wetland extent and fish landings in New South Wales estuaries. Estuar Coast Shelf Sci 61(4):591–601
Saintilan N, Rogers K, Mckee K (2009) Salt marsh-mangrove interactions in Australasia and the Americas. In: G.M Perillo E Wolanski, D. Cahoon & M. Brinson (ed) Coastal wetlands: an integrated ecosystem approach. Elsevier, Amsterdam, pp 855–884
Saintilan N, Wilson NC, Rogers K, Rajkaran A, Krauss KW (2014) Mangrove expansion and salt marsh decline at mangrove poleward limits. Glob Chang Biol 20(1):147–157. doi:10.1111/gcb.12341
Santantonio D, Hermann R (1985) Standing crop, production, and turnover of fine roots on dry, moderate, and wet sites of mature Douglas-fir in western Oregon. Ann Sci For 2:113–142
Sasekumar A, Chong V, Leh M, D’cruz R (1992) Mangroves as a habitat for fish and prawns. Hydrobiologia 247(1–3):195–207
Schaeffer-Novelli Y, Cintrón-Molero G, Adaime RR, de Camargo TM (1990) Variability of mangrove ecosystems along the Brazilian coast. Estuar Coasts 13(2):204–218. doi:10.2307/1351590
Sell MG (1977) Modeling the response of mangrove ecosystems to herbicide spraying, hurricanes, nutrient enrichment and economic development. Ph.D. Thesis, University of Florida, Gainesville, Florida
Sessegolo GC, Lana PC (1991) Decomposition of Rhizophora mangle, Avicennia schaueriana and Laguncularia racemosa leaves in a mangrove of Paranagua Bay (southeastern Brazil). Bot Mar 34:285–289
Sherman RE, Fahey TJ, Martinez P (2003) Spatial patterns of biomass and aboveground net primary productivity in a mangrove ecosystem in the Dominican Republic. Ecosystems 6(4):384–398
Siikamäki J, Sanchirico JN, Jardine SL (2012) Global economic potential for reducing carbon dioxide emissions from mangrove loss. Proc Natl Acad Sci 109(36):14369–14374
Simard M, Rivera-Monroy VH, Mancera-Pineda JE, Castaneda-Moya E, Twilley RR (2008) A systematic method for 3D mapping of mangrove forests based on Shuttle Radar Topography Mission elevation data, ICEsat/GLAS waveforms and field data: application to Cienaga Grande de Santa Marta, Colombia. Remote Sens Environ 112(5):2131–2144. doi:10.1016/J.Rse.2007.10.012
Simard M, Zhang KQ, Rivera-Monroy VH, Ross MS, Ruiz PL, Castaneda-Moya E, Twilley RR, Rodriguez E (2006) Mapping height and biomass of mangrove forests in Everglades National Park with SRTM elevation data. Photogramm Eng Remote Sens 72(3):299–311
Smith TJ, Anderson GH, Balentine K, Tiling G, Ward GA, Whelan KR (2009) Cumulative impacts of hurricanes on Florida mangrove ecosystems: sediment deposition, storm surges and vegetation. Wetlands 29(1):24–34
Snedaker SC, Baquer SJ, Behr PJ, Ahmed SI (1995) Biomass distribution in Avicennia marina plants in the Indus River Delta, Pakistan. In: Thompson MF, Tirmizi NM (eds) The Arabian sea. Vanguard, Lahore, p 724
Sousa W, Dangremond E (2011) Trophic interactions in coastal and estuarine mangrove forest ecosystems. Treatise Estuar Coast Sci 6:43–93
Stieglitz TC, Clark JF, Hancock GJ (2013) The mangrove pump: the tidal flushing of animal burrows in a tropical mangrove forest determined from radionuclide budgets. Geochim Cosmochim Acta 102:12–22
Sukardjo S, Yamada I (1992) Biomass and productivity of a Rhizophora mucronata Lamarck plantation in Tritih, Central Java, Indonesia. For Ecol Manag 49(3–4):195–209
Sutula MA, Perez BC, Reyes E, Childers DL, Davis S, Day JW, Rudnick D, Sklar F (2003) Factors affecting spatial and temporal variability in material exchange between the Southern Everglades wetlands and Florida Bay (USA). Estuar Coast Shelf Sci 57(5):757–781
Tamooh F, Huxham M, Karachi M, Mencuccini M, Kairo J, Kirui B (2008) Below-ground root yield and distribution in natural and replanted mangrove forests at Gazi bay, Kenya. For Ecol Manag 256(6):1290–1297
Thom BG (1982) Mangrove ecology-a geomorphological perspective. In: Clough BF (ed) Mangrove ecosystems in Australia. Australian National University Press, Canberra, pp 3–17
Troxler TG, Barr JG, Fuentes JD, Engel V, Anderson G, Sanchez C, Lagomasino D, Price R, Davis SE (2015) Component-specific dynamics of riverine mangrove CO2 efflux in the Florida coastal Everglades. Agric For Meteorol 213:273–282
Twilley RR (1985) The exchange of organic-carbon in basin mangrove forests in a southwest Florida estuary. Estuar Coast Shelf Sci 20(5):543–557
Twilley RR (1988) Coupling of mangroves to the productivity of estuarine and coastal waters. In: Janson BO (ed) Coastal-offshore ecosystem interactions. Springer, Berlin, pp 155–180
Twilley RR (1995) Properties of mangrove ecosystems related to the energy signature of coastal environments. In: Hall CAS (ed) Maximum power: the ideas and applications of H. T. Odum. University Press of Colorado, Niwot, pp 43–62
Twilley RR, Chen RH, Hargis T (1992) Carbon sinks in mangroves and theirs implications to carbon budget of tropical coastal ecosystems. Water Air Soil Pollut 64:265–288
Twilley RR, Lugo AE, Patterson-Zucca C (1986) Litter production and turnover in basin mangrove forests in southwest Florida. Ecology 67(3):670–683
Twilley RR, Pozo M, Garcia VH, Rivera-Monroy VH, Zambrano R, Bodero A (1997) Litter dynamics in riverine mangrove forests in the Guayas River estuary, Ecuador. Oecologia 111:109–122
Twilley RR, Rivera-Monroy VH (2005) Developing performance measures of mangrove wetlands using simulation models of hydrology, nutrient biogeochemistry, and community dynamics. J Coast Res 40:79–93
Twilley RR, Rivera-Monroy VH (2009) Ecogeomorphic models of nutrient biogeochemistry for mangrove wetlands. Coastal wetlands: an integrated ecosystem approach. Elsevier, Amsterdam, pp 641–683
Valiela I, Bowen JL, York JK (2001) Mangrove forests: one of the world’s threatened major tropical environments. Bioscience 51:807–815
Vogt KA, Vogt DJ, Bloomfield J (1998) Analysis of some direct and indirect methods for estimating root biomass and production of forests at an ecosystem level. Plant Soil 200:71–89
Werry J, Lee S (2005) Grapsid crabs mediate link between mangrove litter production and estuarine planktonic food chains. Mar Ecol Prog Ser 293:165–176
Whelan KRT, Smith TJ, Cahoon DR, Lynch JC, Anderson GH (2005) Groundwater control of mangrove surface elevation: shrink and swell varies with soil depth. Estuaries Coasts 28(6):833–843. doi:10.1007/bf02696013
Woodroffe C (1992) Mangrove sediments and geomorphology. In: Robertson AI, Alongi DM (eds) Coastal and estuarine studies, Chapter 2. American Geophysical Union, Washington, D. C, pp 7–41
Woodroffe CD (1985) Studies of a mangrove basin, Tuff Crater, New Zealand: II. Comparison of volumetric and velocity-area methods of estimating tidal flux. Estuar Coast Shelf Sci 20:431–445
Woodroffe CD (2002) Coasts: form, process and evolution. Cambridge University Press, Cambridge
Woodroffe CD, Bardsley KN, Ward PJ, Hanley JR (1988) Production of mangrove litter in a macrotidal embayment, Darwin Harbour, N.T., Australia. Estuar Coast Shelf Sci 26:581–598
Woodroffe CD, Rogers K, McKee KL, Lovelock CE, Mendelssohn I, Saintilan N (2016) Mangrove sedimentation and response to relative sea-level rise. Annu Rev Mar Sci 8:243–266
Zablocki JA, Andersson AJ, Bates NR (2011) Diel aquatic CO2 system dynamics of a Bermudian mangrove environment. Aquat Geochem 17(6):841–859
Zhang KQ, Simard M, Ross M, Rivera-Monroy VH, Houle P, Ruiz P, Twilley RR, Whelan KRT (2008) Airborne laser scanning quantification of disturbances from hurricanes and lightning strikes to mangrove forests in Everglades National Park, USA. Sensors 8(4):2262–2292
Acknowledgments
This work represents support from several funding sources including the Florida Coastal Everglades Long-Term Ecological Research (FCE-LTER) program funded by the National Science Foundation (Grant #DBI-0620409, Grant #DEB-9910514, and Grant #DEB-1237517), Coastal SEES program of National Science Foundation (EAR-1427389), and Frontiers of Earth Surface Dynamics (OCE-1135427). Support was also provided by Louisiana Sea Grant College Program. ASR was partially supported by CAPES/CNPq Science without Borders Program (grant no. BEX1930/13-3). VHRM was partially funded by NASA-JPL project “Vulnerability Assessment of Mangrove Forest Regions of the Americas” (LSU Subcontract no. 1452878), and the Department of the Interior South Central Climate Science Center through Cooperative Agreement # G12AC00002. We would like to thank Paulo R. Pagliosa from Universidade Federal de Santa Catarina, Florianópolis, Brasil, and Alessandra Larissa Fonseca from Universidade Federal de Santa Catarina, Florianópolis, Brasil in helping to compile some of the mangrove statistics.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2017 Springer International Publishing AG
About this chapter
Cite this chapter
Twilley, R.R., Castañeda-Moya, E., Rivera-Monroy, V.H., Rovai, A. (2017). Productivity and Carbon Dynamics in Mangrove Wetlands. In: Rivera-Monroy, V., Lee, S., Kristensen, E., Twilley, R. (eds) Mangrove Ecosystems: A Global Biogeographic Perspective. Springer, Cham. https://doi.org/10.1007/978-3-319-62206-4_5
Download citation
DOI: https://doi.org/10.1007/978-3-319-62206-4_5
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-62204-0
Online ISBN: 978-3-319-62206-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)