Abstract. Biotic and abiotic factors influence the accumulation of organic carbon (Corg) in seagrass ecosystems. We surveyed Posidonia sinuosa meadows growing in different water depths to assess the variability in the sources, stocks and accumulation rates of Corg. We show that over the last 500 years, P. sinuosa meadows closer to the upper limit of distribution (at 2–4 m depth) accumulated 3- to 4-fold higher Corg stocks (averaging 6.3 kg Corg m−2) at 3- to 4-fold higher rates (12.8 g Corg m−2 yr−1) compared to meadows closer to the deep limits of distribution (at 6–8 m depth; 1.8 kg Corg m−2 and 3.6 g Corg m−2 yr−1). In shallower meadows, Corg stocks were mostly derived from seagrass detritus (88 % in average) compared to meadows closer to the deep limit of distribution (45 % on average). In addition, soil accumulation rates and fine-grained sediment content (< 0.125 mm) in shallower meadows (2.0 mm yr−1 and 9 %, respectively) were approximately 2-fold higher than in deeper meadows (1.2 mm yr−1 and 5 %, respectively). The Corg stocks and accumulation rates accumulated over the last 500 years in bare sediments (0.6 kg Corg m−2 and 1.2 g Corg m−2 yr−1) were 3- to 11-fold lower than in P. sinuosa meadows, while fine-grained sediment content (1 %) and seagrass detritus contribution to the Corg pool (20 %) were 8- and 3-fold lower than in Posidonia meadows, respectively. The patterns found support the hypothesis that Corg storage in seagrass soils is influenced by interactions of biological (e.g., meadow productivity, cover and density), chemical (e.g., recalcitrance of Corg stocks) and physical (e.g., hydrodynamic energy and soil accumulation rates) factors within the meadow. We conclude that there is a need to improve global estimates of seagrass carbon storage accounting for biogeochemical factors driving variability within habitats.
Abstract Posidonia oceanica , a seagrass endemic to the Mediterranean forms extended and extremely persistent meadows. It is a clonal plant with an apparently irregular pattern of flowering events. An extensive bibliographic review allowed the reconstruction of past flowering events of this species around the Mediterranean, with a high degree of confidence for the last 30 years. The data series on annual flowering prevalence (FP, flowering records per total records) and flowering intensity (FI, fraction of flowering shoots) produced have been compared with four series on Sea Surface annual Temperature maxima (SST max ) obtained for the NW Mediterranean (averaged from the local data series of l'Estartit and Villefranche: 1957–2005) and for the Eastern, Western basin and the whole Mediterranean sea (extracted from NCEP Reynolds interpolated SST maps: 1982–2005). Significant warming trends are detected in the Mediterranean SST max series, at a rate of (mean+SE) 0.04±0.01°C yr −1 ( R 2 =0.24, P <0.01, N =24 years), in the Eastern basin series (0.06±0.01°C yr −1 , R 2 =0.43, P <0.001, N =24 years) and in the long SST max series of the NW Mediterranean (0.02±0.01 C yr −1 , R 2 =0.12, P <0.02, N =49 years). The magnitudes of the SST max anomalies around the absolute warming trend do not increase with time in any SST max series. Peaks of FP and FI in the Mediterranean seem to occur each 9–11 years, and coincide with peaks of annual SST max . Annual FP and FI increase with the residuals of annual SST max warming trend in all Mediterranean basins (FP MED : R 2 =0.27, P <0.01, N =23; FP NW : R 2 =0.34, P <0.01, N =31; FP E : R 2 =0.20; P <0.10, N =23). An outstanding event of P. oceanica flowering across the Mediterranean has been registered in Autumn 2003; 1 month after the highest annual SST max recorded in the series. The hypothesis of flowering induction by thermal stress as the possible cause of this relationship is discussed, as well as the potential use of P. oceanica flowering record as early indicator of biological change induced by global sea warming in Mediterranean marine ecosystems.
Community respiration (R) rates are scaled as the two-thirds power of the gross primary production (P) rates of aquatic ecosystems, indicating that the role of aquatic biota as carbon dioxide sources or sinks depends on its productivity. Unproductive aquatic ecosystems support a disproportionately higher respiration rate than that of productive aquatic ecosystems, tend to be heterotrophic (R > P), and act as carbon dioxide sources. The average P required for aquatic ecosystems to become autotrophic (P > R) is over an order of magnitude greater for marshes than for the open sea. Although four-fifths of the upper ocean is expected to be net heterotrophic, this carbon demand can be balanced by the excess production over the remaining one-fifth of the ocean.