The influence of lateral transport on sedimentary alkenone paleoproxy signals

[EN]Alkenone signatures preserved in marine sedimentary records are considered one of the most robust paleothermometers available and are often used as a proxy for paleoproductivity. However, important gaps remain regarding the provenance and fate of alkenones, as well as their impact on derived environmental signals in marine sediments. Here, we analyze the abundance, distribution and radiocarbon (14C) age of alkenones in bulk sediments and corresponding grain-size fractions in surficial sediments from seven continental margin settings in the Pacific and Atlantic oceans to evaluate the impact of organo-mineral associations and hydrodynamic sorting on sedimentary alkenone signals. We find that alkenones preferentially reside within fine-grained mineral fractions of continental margin sediments, with the preponderance of alkenones residing within the fine-silt fraction (2–10 µm) and most strongly influencing alkenone-14C age and sea surface temperature (SST) signals from bulk sediments as a consequence of their proportional abundance and higher degree of organic matter protection relative to other fractions. Our results provide further evidence for the key role of selective association of alkenones with mineral surfaces and associated hydrodynamic mineral sorting processes on the reliability of alkenone signals encoded in marine sediments (14C age, content and distribution) and the fidelity of corresponding proxy records (productivity and sea SST) in the spatial and temporal domain

Coupling of Dye Analysis and Compound Specific Radiocarbon (14C) Analysis (CSRA) in Heritage Sciences

Natural organic dyes and pigments have been used for millennia to bring colour into our daily lives. Being sourced from a variety of natural sources, they form an extremely varied and large class of compounds, all of which retain the atmospheric 14CO2 of their year of growth. As such these compounds represent ideal candidates for radiocarbon (14C) dating, allowing the identification of or providing information towards the period in which the coloured artefact was created. However, up to now no such analysis has ever been conducted solely on organic colourants within an object. The complex nature of the samples and the sample size limitations with respect to precious and rare art artefacts requires innovative inter- and multidisciplinary approaches. Here we discuss preliminary results in the development of a compound-specific radiocarbon analysis (CSRA) methodology for the analysis of anthraquinone derived red dyes extracted from dyed wool yarns. The aim of this research project is to introduce new routes to date cultural heritage objects, in particular to overcome their intrinsic complexity through the development of CSRA strategies

Temporal constraints on lateral organic matter transport along a coastal mud belt

Constraints on timescales of lateral transport of organic carbon (OC) over continental shelves and associated influences on the distribution and abundance of sedimentary OC remain sparse. Preferential degradation of labile, young OC during lateral transport results in apparent “diagenetic aging“ of OC. Additionally, sediment translocation can also result in ”transport time-associated aging“ of associated organic matter (OM) as a function of the lateral transport time (LTT). Here, we use a coupled thermal decomposition and radiocarbon (14C) approach to constrain timescales of lateral transport and concomitant loss of OC associated with different grain size fractions of sediments collected from two locations ∼275 km apart along a dispersal pathway on the inner shelf of the East China Sea. The 14C age contrasts between corresponding thermal fractions are used to distinguish these two components of sedimentary OM “aging”. To minimize interferences from hydrodynamic sorting and diagenetic aging of OC accompanying lateral transport, we assess 14C age differences of decomposition products from the most thermally-refractory OC components associated with specific grain size fractions between locations. We show that LTTs vary among different grain size fractions, and examine relationships between LTTs and sedimentary OC loss in order to assess the decomposition of OC as a consequence of lateral transport. We suggest that the decomposition of OC associated with protracted lateral transport exerts a strong influence on OC burial efficiency, with broad implications for carbon cycling over continental shelves

Short communication: Massive erosion in monsoonal central India linked to late Holocene land cover degradation

Soil erosion plays a crucial role in transferring sediment and carbon from land to sea, yet little is known about the rhythm and rates of soil erosion prior to the most recent few centuries. Here we reconstruct a Holocene erosional history from central India, as integrated by the Godavari River in a sediment core from the Bay of Bengal. We quantify terrigenous fluxes, fingerprint sources for the lithogenic fraction and assess the age of the exported terrigenous carbon. Taken together, our data show that the monsoon decline in the late Holocene significantly increased soil erosion and the age of exported organic carbon. This acceleration of natural erosion was later exacerbated by the Neolithic adoption and Iron Age extensification of agriculture on the Deccan Plateau. Despite a constantly elevated sea level since the middle Holocene, this erosion acceleration led to a rapid growth of the continental margin. We conclude that in monsoon conditions aridity boosts rather than suppresses sediment and carbon export, acting as a monsoon erosional pump modulated by land cover conditions

Millennial soil retention of terrestrial organic matter deposited in the Bengal Fan

© The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Scientific Reports 8 (2018): 11997, doi:10.1038/s41598-018-30091-8.The abundance of organic carbon (OC) in vegetation and soils (~2,600 PgC) compared to carbon in the atmosphere (~830 PgC) highlights the importance of terrestrial OC in global carbon budgets. The residence time of OC in continental reservoirs, which sets the rates of carbon exchange between land and atmosphere, represents a key uncertainty in global carbon cycle dynamics. Retention of terrestrial OC can also distort bulk OC- and biomarker-based paleorecords, yet continental storage timescales remain poorly quantified. Using “bomb” radiocarbon (14C) from thermonuclear weapons testing as a tracer, we model leaf-wax fatty acid and bulk OC 14C signatures in a river-proximal marine sediment core from the Bay of Bengal in order to constrain OC storage timescales within the Ganges-Brahmaputra (G-B) watershed. Our model shows that 79–83% of the leaf-waxes in this core were stored in continental reservoirs for an average of 1,000–1,200 calendar years, while the remainder was stored for an average of 15 years. This age structure distorts high-resolution organic paleorecords across geologically rapid events, highlighting that compound-specific proxy approaches must consider storage timescales. Furthermore, these results show that future environmental change could destabilize large stores of old - yet reactive - OC currently stored in tropical basins.We acknowledge funding support from the Agouron Institute Postdoctoral Fellowship (K.L.F), the US National Science Foundation (Awards: OCE-1333387 and OCE-13333826), the Investment in Science Fund given primarily by WHOI Trustee and Corporation Members, and the Swiss National Science Foundation (Award: 200020_163162)

Detrital Neodymium and (Radio)Carbon as Complementary Sedimentary Bedfellows? The Western Arctic Ocean as a Testbed

Interactions between organic and detrital mineral phases strongly influence both the dispersal and accumulation of terrestrial organic carbon (OC) in continental margin sediments. Yet the complex interplay among biological, chemical, and physical processes limits our understanding of how organo-mineral interactions evolve during sediment transfer and burial. In particular, diverse OC sources and complex hydrodynamic processes hinder the assessment of how the partnership of organic matter and its mineral host evolves during supply and dispersal over continental margins. In this study, we integrate new and compiled sedimentological (grain size, surface area), organic (%OC, OC-δ13C, OC-F14C), and inorganic isotopic (εNd, 87Sr/86Sr) geochemical data for a broad suite of surface sediments spanning the Western Arctic Ocean from the Bering Sea to the Mackenzie River Delta that capture diverse sources and ages of both terrestrial and marine material deposited in contrasting shelf and slope settings. Spatial gradients in sediment properties were used to delineate regional sources and transport processes influencing the dispersion and persistence of OC-mineral particle associations during export and burial. We found strong relationships between physical parameters, aluminum content, and OC-14C suggesting that terrestrial OC remains tightly associated with its detrital mineral carrier during source-to-sink transport. Notably, carbon and neodymium isotopic data yield consistent information regarding organic matter provenance. Results obtained highlight the potential for coupled organic-inorganic tracer measurements to elucidate sediment sources and to constrain physical and geochemical processes during sediment mobilization and transport in the Western Arctic Ocean. Tandem measurements of carbon and Nd isotopes may provide a new way to identify large-scale biogeochemical and ecological changes in the sources, nature, and fate of OC stemming from predicted increases in sea ice loss and fluvial inputs of dissolved and particulate OC to this complex and dynamic high latitude marginal sea

Radiocarbon age offsets between two surface dwelling planktonic foraminifera species during abrupt climate events in the SW Iberian Margin

This study identifies temporal biases in the radiocarbon ages of the planktonic foraminifera species Globigerina bulloides and Globigerinoides ruber (white) in a sediment core from the SW Iberian margin (so‐called Shackleton site). Leaching of the outer shell and measurement of the radiocarbon content of both the leachate and leached sample enabled us to identify surface contamination of the tests and its impact on their 14C ages. Incorporation of younger radiocarbon on the outer shell affected both species and had a larger impact downcore. Interspecies comparison of the 14C ages of the leached samples reveal systematic offsets with 14C ages for G. ruber being younger than G. bulloides ages during the last deglaciation and part of the Early and mid‐Holocene. The greatest offsets (up to 1,030 years) were found during Heinrich Stadial 1, the Younger Dryas, and part of the Holocene. The potential factors differentially affecting these two planktonic species were assessed by complementary 14C, oxygen and carbon isotopes, and species abundance determinations. The coupled effect of bioturbation with changes in the abundance of G. ruber is invoked to account for the large age offsets. Our results highlight that 14C ages of planktonic foraminifera might be largely compromised even in settings characterized by high sediment accumulation rates. Thus, a careful assessment of potential temporal biases must be performed prior to using 14C ages for paleoclimate investigations or radiocarbon calibrations (e.g., marine calibration curve Marine13, Reimer et al., 2013, https://doi.org/10.2458/azu_js_rc.55.16947).UID/Multi/04326/2019, IF/01500/2014info:eu-repo/semantics/publishedVersio

What on Earth have we been burning? Deciphering sedimentary records of pyrogenic carbon

Humans have interacted with fire for thousands of years, yet the utilization of fossil fuels marked the beginning of a new era. Ubiquitous in the environment, pyrogenic carbon (PyC) arises from incomplete combustion of biomass and fossil fuels, forming a continuum of condensed aromatic structures. Here we develop and evaluate 14C records for two complementary PyC molecular markers, benzene-polycarboxylic-acids (BPCAs) and polycyclic-aromatic-hydrocarbons (PAHs) preserved in aquatic sediments from a sub-urban and a remote catchment in the United States (U.S.) from mid-1700s to 1998. Results show that the majority of PyC stems from local sources and is transferred to aquatic sedimentary archives on sub-decadal to millennial time scales. Whereas a small portion stems from near-contemporaneous production and sedimentation, the majority of PyC (<90%) experiences delayed transmission due to ‘pre-aging’ on millennial timescales in catchment soils prior to its ultimate deposition. BPCAs (soot) and PAHs (precursors of soot) trace fossil fuel-derived PyC. Both markers parallel historical records of the consumption of fossil fuels in U.S., yet never account for more than 19% total PyC. This study demonstrates that isotopic characterization of multiple tracers is necessary to constrain histories and inventories of PyC, and that sequestration of PyC can markedly lag its production

Dynamics of deep soil carbon – insights from 14C time series across a climatic gradient

Quantitative constraints on soil organic matter (SOM) dynamics are essential for comprehensive understanding of the terrestrial carbon cycle. Deep soil carbon is of particular interest as it represents large stocks and its turnover times remain highly uncertain. In this study, SOM dynamics in both the top and deep soil across a climatic (average temperature ∼ 1–9 ∘C) gradient are determined using time-series (∼20 years) 14C data from bulk soil and water-extractable organic carbon (WEOC). Analytical measurements reveal enrichment of bomb-derived radiocarbon in the deep soil layers on the bulk level during the last 2 decades. The WEOC pool is strongly enriched in bomb-derived carbon, indicating that it is a dynamic pool. Turnover time estimates of both the bulk and WEOC pool show that the latter cycles up to a magnitude faster than the former. The presence of bomb-derived carbon in the deep soil, as well as the rapidly turning WEOC pool across the climatic gradient, implies that there likely is a dynamic component of carbon in the deep soil. Precipitation and bedrock type appear to exert a stronger influence on soil C turnover time and stocks as compared to temperature

Online 13C and 14C gas measurements by EA-IRMS–AMS at ETH Zürich

Studies using carbon isotopes to understand the global carbon cycle are critical to identify and quantify sources, sinks, and processes and how humans may impact them. 13C and 14C are routinely measured individually; however, there is a need to develop instrumentation that can perform concurrent online analyses that can generate rich data sets conveniently and efficiently. To satisfy these requirements, we coupled an elemental analyzer to a stable isotope mass spectrometer and an accelerator mass spectrometer system fitted with a gas ion source. We first tested the system with standard materials and then reanalyzed a sediment core from the Bay of Bengal that had been analyzed for 14C by conventional methods. The system was able to produce %C, 13C, and 14C data that were accurate and precise, and suitable for the purposes of our biogeochemistry group. The system was compact and convenient and is appropriate for use in a range of fields of research