ALBERT

Description: Compound-specific radiocarbon (14C) dating often requires working with small samples of 〈 100 µg carbon (µgC). This makes the radiocarbon dates of biomarker compounds very sensitive to biases caused by extraneous carbon of unknown composition, a procedural blank, which is introduced to the samples during the steps necessary to prepare a sample for radiocarbon analysis by accelerator mass spectrometry (i.e., isolating single compounds from a heterogeneous mixture, combustion, gas purification and graphitization). Reporting accurate radiocarbon dates thus requires a correction for the procedural blank. We present our approach to assess the fraction modern carbon (F14C) and the mass of the procedural blanks introduced during the preparation procedures of lipid biomarkers (i.e. n-alkanoic acids) and lignin phenols. We isolated differently sized aliquots (6–151 µgC) of n-alkanoic acids and lignin phenols obtained from standard materials with known F14C values. Each compound class was extracted from two standard materials (one fossil, one modern) and purified using the same procedures as for natural samples of unknown F14C. There is an inverse linear relationship between the measured F14C values of the processed aliquots and their mass, which suggests constant contamination during processing of individual samples. We use Bayesian methods to fit linear regression lines between F14C and 1/mass for the fossil and modern standards. The intersection points of these lines are used to infer F14Cblank and mblank and their associated uncertainties. We estimate 4.88 ± 0.69 μgC of procedural blank with F14C of 0.714 ± 0.077 for n-alkanoic acids, and 0.90 ± 0.23 μgC of procedural blank with F14C of 0.813 ± 0.155 for lignin phenols. These F14Cblank and mblank can be used to correct AMS results of lipid and lignin samples by isotopic mass balance. This method may serve as a standardized procedure for blank assessment in small-scale radiocarbon analysis.

Description: Highlights • Continental margin-scale spatial variability in C values among grain size fractions is presented. • Two different hydrodynamic modes influencing in 14C heterogeneity are identified. • A new index (H14 index) is defined to describe overall 14C heterogeneity within marine surface sedimentary OC. Abstract The deposition and long-term burial of sedimentary organic matter (OM) on continental margins comprises a fundamental component of the global carbon cycle. A key unknown in interpretation of carbon isotope records of sedimentary OM is the extent to which OM accumulating in continental shelf and slope sediments is influenced by dispersal and redistribution processes. Here, we present results from an extensive survey of organic carbon (OC) characteristics of grain size fractions (ranging from 〈20 to 250 μm) retrieved from Chinese marginal sea surface sediments in order to assess the extent to which the abundance and isotope composition of OM in shallow shelf seas is influenced by hydrodynamic processes. Our findings show that contrasting relationships exist between 14C contents of OC and grain size in surface sediments associated with two different hydrodynamic modes, suggesting that transport pathways and mechanisms imparted by the different hydrodynamic conditions exert a strong influence on 14C contents of OM in continental shelf sediments. In deeper regions and erosional areas, we infer that bedload transport exerts the strongest influence on (decreases) OC 14C contents of the coarser fraction, while resuspension processes induce OC 14C depletion of intermediate grain size fractions in shallow inner-shelf settings. We use the inter-fraction spread in 14C values, defined here as 14H , to argue that the hydrodynamic processes amplify overall 14C heterogeneity within corresponding bulk sediment samples. The magnitude and footprint of this heterogeneity carries implications for our understanding of carbon cycling in shallow marginal seas.