(Table S1) Diatom abundance in coastal upwelling systems

Coastal upwelling systems account for approximately half of global ocean primary production and contribute disproportionately to biologically driven carbon sequestration. Diatoms, silica-precipitating microalgae, constitute the dominant phytoplankton in these productive regions, and their abundance and assemblage composition in the sedimentary record is considered one of the best proxies for primary production. The study of the sedimentary diatom abundance (SDA) and total organic carbon content (TOC) in the five most important coastal upwelling systems of the modern ocean (Iberia-Canary, Benguela, Peru-Humboldt, California and Somalia-Oman) reveals a global-scale positive relationship between diatom production and organic carbon burial. The analysis of SDA in conjunction with environmental variables of coastal upwelling systems such as upwelling strength, satellite-derived net primary production and surface water nutrient concentrations shows different relations between SDA and primary production on the regional scale. At the global-scale, SDA appears modulated by the capacity of diatoms to take up silicic acid, which ultimately sets an upper limit to global export production in these ocean regions.

Mesocosm bloom experiment results with the coccolithophore Emiliania huxleyi

We investigated the effect of CO2 and primary production on the carbon isotopic fractionation of alkenones and particulate organic matter (POC) during a natural phytoplankton bloom dominated by the coccolithophore Emiliania huxleyi. In nine semi-closed mesocosms (~11 m**3 each), three different CO2 partial pressures (pCO2) in triplicate represented glacial (~180 ppmv CO2), present (380 ppmv CO2), and year 2100 (~710 ppmv CO2) CO2 conditions. The largest shift in alkenone isotopic composition (4-5 per mil) occurred during the exponential growth phase, regardless of the CO2 concentration in the respective treatment. Despite the difference of ~500 ppmv, the influence of pCO2 on isotopic fractionation was marginal (1-2 per mil). During the stationary phase, E. huxleyi continued to produce alkenones, accumulating cellular concentrations almost four times higher than those of exponentially dividing cells. Our isotope data indicate that, while alkenone production was maintained, the interaction of carbon source and cellular uptake dynamics by E. huxleyi reached a steady state. During stationary phase, we further observed a remarkable increase in the difference between d13C of bulk organic matter and of alkenones spanning 7-12 per mil. We suggest that this phenomenon is caused mainly by a combination of extracellular release of 13C-enriched polysaccharides and subsequent particle aggregation induced by the production of transparent exopolymer particles (TEP).

(Table T1) Geochemical composition of ODP Site 177-1089 sediments

A primary objective of Ocean Drilling Program Leg 177 was to document changes in circulation and biogeochemical cycling on glacial/interglacial time scales across a wide latitudinal range of the south Atlantic Ocean. One of the more northerly sites drilled, Site 1089 (41°S, 10°E), is located within the present-day Subantarctic Zone, south of the Subtropical Front. The drilling site itself is located in the southern Cape Basin at a water depth of 4620 m. Pleistocene sediments at this site are dominated by interbedded carbonate and opal oozes. Initial shipboard stratigraphy identified the opal-rich sediments as deposited during glacial intervals and the carbonate-rich sediments as deposited during interglacial intervals (Gersonde, Hodell, Blum, et al., 1999, doi:10.2973/odp.proc.ir.177.1999). Postcruise isotopic stratigraphy, however, verified that this site displayed a Pacific Pleistocene sedimentation pattern with glacial intervals marked by high carbonate content (Hodell and Charles, 1999). To assess changes in biological productivity and terrigenous inputs at this site, a number of geochemical indicators were determined. Phosphorus concentrations and P/metal ratios were determined to assess changes in export production on glacial/interglacial time scales. Metal concentrations, along with elemental ratios, were used to assess terrigenous inputs. Sediment geochemistry allows us to identify changes in the lithologic component using elemental data based on Fe, Al, and Ti concentrations. Records of concentrations and ratios of biologically related elements identify changes in export production. The P and metal results are important to assess the glacial/interglacial changes in P burial and the relationships between a major nutrient such as P with metals (and possibly trace nutrients) like Fe.