Seagrass sediments as a global carbon sink: Isotopic constraints

Seagrass meadows are highly productive habitats found along many of the world's coastline, providing important services that support the overall functioning of the coastal zone. The organic carbon that accumulates in seagrass meadows is derived not only from seagrass production but from the trapping of other particles, as the seagrass canopies facilitate sedimentation and reduce resuspension. Here we provide a comprehensive synthesis of the available data to obtain a better understanding of the relative contribution of seagrass and other possible sources of organic matter that accumulate in the sediments of seagrass meadows. The data set includes 219 paired analyses of the carbon isotopic composition of seagrass leaves and sediments from 207 seagrass sites at 88 locations worldwide. Using a three source mixing model and literature values for putative sources, we calculate that the average proportional contribution of seagrass to the surface sediment organic carbon pool is ∼50%. When using the best available estimates of carbon burial rates in seagrass meadows, our data indicate that between 41 and 66 gC m−2 yr−1 originates from seagrass production. Using our global average for allochthonous carbon trapped in seagrass sediments together with a recent estimate of global average net community production, we estimate that carbon burial in seagrass meadows is between 48 and 112 Tg yr−1, showing that seagrass meadows are natural hot spots for carbon sequestration.

[1]  N. Marbà,et al.  Seagrass community metabolism: Assessing the carbon sink capacity of seagrass meadows , 2010 .

[2]  K. Mueller,et al.  Global patterns in leaf 13C discrimination and implications for studies of past and future climate , 2010, Proceedings of the National Academy of Sciences.

[3]  Frederick T. Short,et al.  Accelerating loss of seagrasses across the globe threatens coastal ecosystems , 2009, Proceedings of the National Academy of Sciences.

[4]  Janet Rethemeyer,et al.  Selective preservation of organic matter in marine environments; processes and impact on the sedimentary record , 2009 .

[5]  G. Kendrick,et al.  Trophic Transfers from Seagrass Meadows Subsidize Diverse Marine and Terrestrial Consumers , 2008, Ecosystems.

[6]  L. Guasch,et al.  Very high‐resolution seismo‐acoustic imaging of seagrass meadows (Mediterranean Sea): Implications for carbon sink estimates , 2008 .

[7]  C. Duarte,et al.  Experimental assessment and modeling evaluation of the effects of the seagrass Posidonia oceanica on flow and particle trapping , 2008 .

[8]  Rod M. Connolly,et al.  Organic matter exchange and cycling in mangrove ecosystems: Recent insights from stable isotope studies , 2008 .

[9]  Frederick T. Short,et al.  A Global Crisis for Seagrass Ecosystems , 2006 .

[10]  H. Kennedy,et al.  Using variation in the chemical and stable isotopic composition of Zostera noltii to assess nutrient dynamics in a temperate seagrass meadow , 2006 .

[11]  H. Boschker,et al.  Bacterial carbon sources in coastal sediments: a cross-system analysis based on stable isotope data of biomarkers , 2006 .

[12]  N. Marbà,et al.  Modeling nonlinear seagrass clonal growth: Assessing the efficiency of space occupation across the seagrass flora , 2006 .

[13]  E. Koch,et al.  Fluid Dynamics in Seagrass Ecology—from Molecules to Ecosystems , 2006 .

[14]  H. Kennedy,et al.  Seasonal and spatial variation in the organic carbon and nitrogen concentration and their stable isotopic composition in Zostera marina (Denmark) , 2005 .

[15]  N. Marbà,et al.  Sources of organic matter in seagrass-colonized sediments: A stable isotope study of the silt and clay fraction from Posidonia oceanica meadows in the western Mediterranean. , 2005 .

[16]  J. Fourqurean,et al.  Spatial and seasonal variability in elemental content, δ13C, and δ15N ofThalassia testudinum from South Florida and its implications for ecosystem studies , 2005 .

[17]  S. Papadimitriou,et al.  The effect of acidification on the determination of organic carbon, total nitrogen and their stable isotopic composition in algae and marine sediment. , 2005, Rapid communications in mass spectrometry : RCM.

[18]  Jack J. Middelburg,et al.  Major role of marine vegetation on the oceanic carbon cycle , 2004 .

[19]  N. Marbà,et al.  Recolonization dynamics in a mixed seagrass meadow: The role of clonal versus sexual processes , 2004 .

[20]  H. Kennedya,et al.  Organic carbon sources to SE Asian coastal sediments , 2004 .

[21]  J. Fourqurean,et al.  Changes in nutrient content and stable isotope ratios of C and N during decomposition of seagrasses and mangrove leaves along a nutrient availability gradient in Florida Bay, USA , 2003 .

[22]  D. Phillips,et al.  Source partitioning using stable isotopes: coping with too many sources , 2003, Oecologia.

[23]  C. Duarte,et al.  Evidence of direct particle trapping by a tropical seagrass meadow , 2002 .

[24]  J. Middelburg,et al.  Carbon and nutrient deposition in a Mediterranean seagrass (Posidonia oceanica) meadow , 2002 .

[25]  M. Sullivan,et al.  Trophic importance of epiphytic algae in subtropical seagrass beds: evidence from multiple stable isotope analyses , 2001 .

[26]  C. Duarte,et al.  Sediment Retention by a Mediterranean Posidonia oceanica Meadow: The Balance between Deposition and Resuspension , 2001 .

[27]  C. Duarte,et al.  Experimental evidence of reduced particle resuspension within a seagrass (Posidonia oceanica L.) meadow , 2000 .

[28]  C. Kendall,et al.  Geochemistry of Florida Bay Sediments: Nutrient History at Five Sites in Eastern and Central Florida Bay , 1999 .

[29]  R. O'Neill,et al.  The value of the world's ecosystem services and natural capital , 1997, Nature.

[30]  Carlos M. Duarte,et al.  The fate of marine autotrophic production , 1996 .

[31]  R. Goericke,et al.  Variations of marine plankton δ13C with latitude, temperature, and dissolved CO2 in the world ocean , 1994 .

[32]  A. Sournia,et al.  The comparative estimation of phytoplanktonic, microphytobenthic and macrophytobenthic primary production in the oceans , 1990 .

[33]  H. Wanless,et al.  Origin, growth and evolution of carbonate mudbanks in Florida Bay , 1989 .

[34]  W. Woelkerling,et al.  Quantitative study of sediment contribution by epiphytic coralline red algae in seagrass meadows in Shark Bay, Western Australia , 1988 .

[35]  W. Kenworthy,et al.  Production and decomposition of the roots and rhizomes of seagrasses, Zostera marina and Thallassia testudinum, in temperate and subtropical marine ecosystems , 1984 .

[36]  A. Mills,et al.  Role of seagrasses and mangroves in estuarine food webs: temporal and spatial changes in stable isotope composition and amino acid content during decomposition , 1984 .

[37]  S. V. Smith Marine macrophytes as a global carbon sink. , 1981, Science.

[38]  B. Fry,et al.  Stable carbon isotope evidence for two sources of organic matter in coastal sediments: seagrasses and plankton , 1977 .

[39]  R. Iverson,et al.  Thalassia testudinum productivity: A field comparison of measurement methods , 1976 .

[40]  H. Craig THE GEOCHEMISTRY OF THE STABLE CARBON ISOTOPES , 1953 .