[1] Nitrogen isotopes are an important tool for evaluating past biogeochemical cycling from the paleoceanographic record. However, bulk sedimentary nitrogen isotope ratios, which can be determined routinely and at minimal cost, may be altered during burial and early sedimentary diagenesis, particularly outside of continental margin settings. The causes and detailed mechanisms of isotopic alteration are still under investigation. Case studies of the Mediterranean and South China Seas underscore the complexities of investigating isotopic alteration. In an effort to evaluate the evidence for alteration of the sedimentary N isotopic signal and try to quantify the net effect, we have compiled and compared data demonstrating alteration from the published literature. A >100 point comparison of sediment trap and surface sedimentary nitrogen isotope values demonstrates that, at sites located off of the continental margins, an increase in sediment 15 N/ 14 N occurs during early burial, likely at the seafloor. The extent of isotopic alteration appears to be a function of water depth. Depth-related differences in oxygen exposure time at the seafloor are likely the dominant control on the extent of N isotopic alteration. Moreover, the compiled data suggest that the degree of alteration is likely to be uniform through time at most sites so that bulk sedimentary isotope records likely provide a good means for evaluating relative changes in the global N cycle.Citation: Robinson, R. S., et al. (2012), A review of nitrogen isotopic alteration in marine sediments, Paleoceanography, 27, PA4203,
The lipid extracts of sediments collected from the Quaternary filling of a tropical lacustrine series (Lagoa do Caçó, Brazil) were investigated by gas chromatography-mass spectrometry (GC-MS). Various pentacyclic triterpene 3-methyl ethers (PTMEs) were present in the neutral fraction. Comparison of retention times and mass spectra with available standards allowed us to certify the presence of olean-12-en-3β-ol ME (β-amyrin ME), olean-18-en-3β-ol ME (miliacin), taraxer-14-en-3β-ol ME (crusgallin), fern-9(11)-en-3β-ol ME (arundoin) and arbor-9(11)-en-3β-ol ME (cylindrin). The following other compounds coud also be tentatively identified from their GC-MS characteristics: urs-12-en-3β-ol ME, bauer-7-en-3β-ol ME and fern-8-en-3β-ol ME. Other compounds such as possible 3α isomers of the PTMEs as well as di-or tri-unsaturated counterparts might be PTME diagenetic derivatives. According to previous chemotaxonomic studies, all these compounds most probably originate from Gramineae that used to colonize the savannas of Northern Brazil at the time of deposition.
Rapid changes in ocean circulation and climate have been observed in marine-sediment and ice cores over the last glacial period and deglaciation, highlighting the non-linear character of the climate system and underlining the possibility of rapid climate shifts in response to anthropogenic greenhouse gas forcing. To date, these rapid changes in climate and ocean circulation are still not fully explained. One obstacle hindering progress in our understanding of the interactions between past ocean circulation and climate changes is the difficulty of accurately dating marine cores. Here, we present a set of 92 marine sediment cores from the Atlantic Ocean for which we have established age-depth models that are consistent with the Greenland GICC05 ice core chronology, and computed the associated dating uncertainties, using a new deposition modeling technique. This is the first set of consistently dated marine sediment cores enabling paleoclimate scientists to evaluate leads/lags between circulation and climate changes over vast regions of the Atlantic Ocean. Moreover, this data set is of direct use in paleoclimate modeling studies.
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