Coupled changes in western South Atlantic carbon sequestration and particle reactive element cycling during millennial-scale Holocene climate variability.

ABSTRACT: Continental shelves have the potential to remove atmospheric carbon dioxide via the biological pump, burying it in seafloor sediments. The efficiency of marine carbon sequestration changes rapidly due to variations in biological productivity, organic carbon oxidation, and burial rate. Here we present a high temporal resolution record of marine carbon sequestration changes from a western South Atlantic shelf site sensitive to Brazil Current-driven upwelling. The comparison of biological records to rare earth element (REE) patterns from authigenic oxides shows a strong relationship between higher biological productivity and stronger particle reactive element cycling (i.e. REE cycling) during rapid climate change events. This is the first evidence that authigenic oxides archive past changes in upper ocean REE cycling by the exported organic carbon. In addition, our data suggest that Brazil Current-driven upwelling varies on millennial-scales and in time with continental precipitation anomalies as registered in Brazilian speleothems during the Holocene. This indicates an ocean-atmosphere control on the biological pump, most probably related to South American monsoon system variability.

Protective effects of melatonin-loaded lipid-core nanocapsules on paraquat-induced cytotoxicity and genotoxicity in a pulmonary cell line.

Many acute poisonings lack effective and specific antidotes. Due to both intentional and accidental exposures, paraquat (PQ) causes thousands of deaths annually, especially by pulmonary fibrosis. Melatonin (Mel), when incorporated into lipid-core nanocapsules (Mel-LNC), has enhanced antioxidant properties. The effects of such a formulation have not yet been studied with respect to mitigation of PQ- induced cytotoxicity and DNA damage. Here, we have tested whether Mel-LNC can ameliorate PQ-induced toxicity in the A549 alveolar epithelial cell line. Physicochemical characterization of the formulations was performed. Cellular uptake was measured using nanocapsules marked with rhodamine B. Cell viability was determined by the MTT assay and DNA damage was assessed by the comet assay. The enzyme-modified comet assay with endonuclease III (Endo III) and formamidopyrimidine glycosylase (FPG) were used to investigate oxidative DNA damage. Incubation with culture medium for 24h did not alter the granulometric profile of Mel-LNC formulations. Following treatment (3 and 24h), red fluorescence was detected around the cell nucleus, indicating internalization of the formulation. Melatonin solution (Mel), Mel-LNC, and LNC did not have significant effects on cell viability or DNA damage. Pre-treatment with Mel-LNC enhanced cell viability and showed a remarkable reduction in % DNA in tail compared to the PQ group; this was not observed in cells pre-treated with Mel. PQ induces oxidative DNA damage detected with the enzyme-modified comet assay. Mel-LNC reduced this damage more effectively than did Mel. In summary, Mel-LNC is better than Mel at protecting A549 cells from the cytotoxic and genotoxic effects of PQ.