The deposition of phosphorus (P) from African dust is believed to play an important role in bolstering primary productivity in the Amazon Basin and Tropical Atlantic Ocean (TAO), leading to sequestration of carbon dioxide. However, there are few measurements of African dust in South America that can robustly test this hypothesis and even fewer measurements of soluble P, which is readily available for stimulating primary production in the ocean. To test this hypothesis, we measured total and soluble P in long-range transported aerosols collected in Cayenne, French Guiana, a TAO coastal site located at the northeastern edge of the Amazon. Our measurements confirm that in boreal spring when African dust transport is greatest, dust supplies the majority of P, of which 5% is soluble. In boreal fall, when dust transport is at an annual minimum, we measured unexpectedly high concentrations of soluble P, which we show is associated with the transport of biomass burning (BB) from southern Africa. Integrating our results into a chemical transport model, we show that African BB supplies up to half of the P deposited annually to the Amazon from transported African aerosol. This observational study links P-rich BB aerosols from Africa to enhanced P deposition in the Amazon. Contrary to current thought, we also show that African BB is a more important source of soluble P than dust to the TAO and oceans in the Southern Hemisphere and may be more important for marine productivity, particularly in boreal summer and fall.

Ooid formation remains elusive despite their importance as palaeoclimatic indicators and important contributors to global carbonate budget. Based on stable isotopes, nutrient and elemental analyses on solid components and ooidal leachates, this study supports the notion of microbial involvement in the development of ooids from Great Bahama Bank. Carbon and nitrogen isotopic analyses on organic fractions identified geochemical signatures of microbial activity. The δ13C values for organic carbon in the bulk (−11·9 to −16·9‰); intercrystalline/intracrystalline (−11·9 to 16·7‰); and intracrystalline phases (−12·4 to −17·7‰) were similar and, except for the more enriched values of ooids from Butterfly Beach, were within the range of photosynthesisers. The δ15N values for the bulk (+0·5 to −0·2‰); intercrystalline/intracrystalline (−0·3‰ to −0·7‰) and intracrystalline organic matter (−0·3 to −1·7‰) showed a narrow range consistent with nitrogen fixation. While positive δ15N and δ18O values of the NO3− leached from the ooids provided evidence of denitrification, the carbonate associated sulphate δ34SCAS of the bulk sediments (+19·2 to +19·6‰) and δ34S of the leachates (+16·6 to +18·3‰) provided weak indication of sulphate reduction, suggesting either that high concentrations of isotopically enriched S are overriding bio‐signatures of sulphate reduction or that microbes are preferentially using NO3− as an electron acceptor. In contrast, the elevated sulphate concentrations of the leachates suggest the occurrence of microbial sulphide oxidation within ooids. The high Mg/Ca of the leachates and scanning electron microscope analyses provide putative evidence of amorphous calcium carbonate and a formative role in CaCO3 precipitation. Together, these findings indicate that a redox dependent microbial consortium may influence CaCO3 precipitation in the form of ooid accretion, cementation and micritization. It is also inferred that ooid deposits are not suitable indicators of palaeoclimate because ooids are affected throughout their life by a complex chain of abiotic and biological processes which can lead to large geochemical offsets.

Many negative d 13 C excursions in marine carbonates from the geological record are interpreted to record significant biogeochemical events in early Earth history. The assumption that no post-depositional processes can simultaneously alter carbonate and organic d 13 C values towards more negative values is the cornerstone of this approach. However, the effects of post-depositional alteration on the relationship between carbonate and organic d 13 C values have not been directly evaluated. Here we present paired carbonate and organic d 13 C records that exhibit a coupled negative excursion resulting from multiple periods of meteoric alteration of the carbonate d 13 C record, and consequent contributions of isotopically negative terrestrial organic matter to the sedimentary record. The possibility that carbonate and organic d 13 C records can be simultaneously shifted towards lower d 13 C values during periods of subaerial exposure may necessitate the reappraisal of some of the d 13 C anomalies associated with noteworthy biogeochemical events throughout Earth history.

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In pelagic carbonate sediments, the degree to which the δ13C values of inorganic and organic fractions co‐vary has been used to interpret rates of production, burial and decomposition of organic carbon. This relationship is relatively consistent through time, permitting estimates of organic carbon production and preservation. However, as the majority of pelagic sediments older than 200 Myr have been subducted, carbonate sediments deposited in epeiric seas and platforms are often substituted for pelagic carbonates in analyses of ancient global carbon cycling. There are well‐known pitfalls to using shallow marine carbonate materials, including diagenesis, semi‐isolation of depositional environments and input of different types of sediments with varying inorganic δ13C (δ13Cinorganic) values, which can obscure any global signatures. One method used to assess whether global changes in δ13C are accurately represented by δ13Cinorganic records is to examine variations in the δ13C of co‐occurring organic material (δ13Corganic). If a δ13Corganic record co‐varies with a co‐occurring δ13Cinorganic record, it is argued that the signals must be related to variations in the global carbon cycle. This assumption has been investigated by analysing the isotopic composition of the organic carbon preserved in the uppermost 150 m of periplatform sediments recovered during ODP Leg 166 from the western margin of Great Bahama Bank. The δ13Corganic values measured in this study were compared to previously published δ13Cinorganic records measured on identical samples, thus allowing a study of the correlation between the two records through time. These analyses showed that the correlation coefficient between δ13Cinorganic and δ13Corganic increased from the proximal location (Site 1005, r2 = 0·1), to the distal site (Site 1006, r2 = 0·63). The importance of platform‐derived carbonate and organic material at the proximal location, Site 1005, is reflected in the absence of a co‐variation between inorganic and organic δ13C records, which exhibit no correlation on the platform itself. In contrast, the co‐variance in δ13C values at the basinal location, Site 1006, is explained by a two‐point mixing model, which demonstrates the importance of both pelagic and platform‐derived carbonate and organic carbon in generating the positive correlation between the organic and inorganic δ13C values; this results in a correlation between δ13Cinorganic and δ13Corganic records at Site 1006 that is unrelated to global carbon cycling. Such data question the applicability of using δ13Corganic values to support the ability of δ13Cinorganic values to record global carbon cycling in carbonates recovered from environments where multiple sources of carbonate and organic carbon contribute to the bulk δ13C signal.