Influence of Different Acid Treatments on the Radiocarbon Content Spectrum of Sedimentary Organic Matter Determined by RPO/Accelerator Mass Spectrometry

Radiocarbon ◽  
2018 ◽  
Vol 61 (2) ◽  
pp. 395-413 ◽  
Author(s):  
Rui Bao ◽  
Ann P McNichol ◽  
Jordon D Hemingway ◽  
Mary C Lardie Gaylord ◽  
Timothy I Eglinton

ABSTRACTIn practice, obtaining radiocarbon (14C) composition of organic matter (OM) in sediments requires first removing inorganic carbon (IC) by acid-treatment. Two common treatments are acid rinsing and fumigation. Resulting14C content obtained by different methods can differ, but underlying causes of these differences remain elusive. To assess the influence of different acid-treatments on14C content of sedimentary OM, we examine the variability in14C content for a range of marine and river sediments. By comparing results for unacidified and acidified sediments [HCl rinsing (RinseHCl) and HCl fumigation (FumeHCl)], we demonstrate that the two acid-treatments can affect14C content differentially. Our findings suggest that, for low-carbonate samples, RinseHClaffects the Fm values due to loss of young labile organic carbon (OC). FumeHClmakes the Fm values for labile OC decrease, leaving the residual OC older. High-carbonate samples can lose relatively old organic components during RinseHCl, causing the Fm values of remaining OC to increase. FumeHClcan remove thermally labile, usually young, OC and reduce the Fm values. We suggest three factors should be taken into account when using acid to remove carbonate from sediments: IC abundance, proportions of labile and refractory OC, and environmental matrix.

Radiocarbon ◽  
2003 ◽  
Vol 45 (1) ◽  
pp. 17-24 ◽  
Author(s):  
Naohiko Ohkouchi ◽  
Timothy I Eglinton ◽  
John M Hayes

We have measured the radiocarbon contents of individual, solvent-extractable, short-chain (C14, C16, and C18) fatty acids isolated from Ross Sea surface sediments. The corresponding 14C ages are equivalent to that of the post-bomb dissolved inorganic carbon (DIC) reservoir. Moreover, molecular 14C variations in surficial (upper 15 cm) sediments indicate that these compounds may prove useful for reconstructing chronologies of Antarctic margin sediments containing uncertain (and potentially variable) quantities of relict organic carbon. A preliminary molecular 14C chronology suggests that the accumulation rate of relict organic matter has not changed during the last 500 14C yr. The focus of this study is to determine the validity of compound-specific 14C analysis as a technique for reconstructing chronologies of Antarctic margin sediments.


2008 ◽  
Vol 1 (1) ◽  
pp. 17-51 ◽  
Author(s):  
G. Shaffer ◽  
S. Malskær Olsen ◽  
J. O. Pepke Pedersen

Abstract. A new, low-order Earth System Model is described, calibrated and tested against Earth system data. The model features modules for the atmosphere, ocean, ocean sediment, land biosphere and lithosphere and has been designed to simulate global change on time scales of years to millions of years. The atmosphere module considers radiation balance, meridional transport of heat and water vapor between low-mid latitude and high latitude zones, heat and gas exchange with the ocean and sea ice and snow cover. Gases considered are carbon dioxide and methane for all three carbon isotopes, nitrous oxide and oxygen. The ocean module has 100 m vertical resolution, carbonate chemistry and prescribed circulation and mixing. Ocean biogeochemical tracers are phosphate, dissolved oxygen, dissolved inorganic carbon for all three carbon isotopes and alkalinity. Biogenic production of particulate organic matter in the ocean surface layer depends on phosphate availability but with lower efficiency in the high latitude zone, as determined by model fit to ocean data. The calcite to organic carbon rain ratio depends on surface layer temperature. The semi-analytical, ocean sediment module considers calcium carbonate dissolution and oxic and anoxic organic matter remineralisation. The sediment is composed of calcite, non-calcite mineral and reactive organic matter. Sediment porosity profiles are related to sediment composition and a bioturbated layer of 0.1 m thickness is assumed. A sediment segment is ascribed to each ocean layer and segment area stems from observed ocean depth distributions. Sediment burial is calculated from sedimentation velocities at the base of the bioturbated layer. Bioturbation rates and oxic and anoxic remineralisation rates depend on organic carbon rain rates and dissolved oxygen concentrations. The land biosphere module considers leaves, wood, litter and soil. Net primary production depends on atmospheric carbon dioxide concentration and remineralization rates in the litter and soil are related to mean atmospheric temperatures. Methane production is a small fraction of the soil remineralization. The lithosphere module considers outgassing, weathering of carbonate and silicate rocks and weathering of rocks containing old organic carbon and phosphorus. Weathering rates are related to mean atmospheric temperatures. A pre-industrial, steady state calibration to Earth system data is carried out. Ocean observations of temperature, carbon 14, phosphate, dissolved oxygen, dissolved inorganic carbon and alkalinity constrain air-sea exchange and ocean circulation, mixing and biogeochemical parameters. Observed calcite and organic carbon distributions and inventories in the ocean sediment help constrain sediment module parameters. Carbon isotopic data and carbonate vs. silicate weathering fractions are used to estimate initial lithosphere outgassing and rock weathering rates. Model performance is tested by simulating atmospheric greenhouse gas increases, global warming and model tracer evolution for the period 1765 to 2000, as forced by prescribed anthropogenic greenhouse gas inputs and other anthropogenic and natural forcing. Long term, transient model behavior is studied with a set of 100 000 year simulations, forced by a slow, 5000 Gt C input of CO2 to the atmosphere, and with a 1.5 million year simulation, forced by a doubling of lithosphere CO2 outgassing.


2020 ◽  
Author(s):  
Ni Tang ◽  
Nina Siebers ◽  
Erwin Klumpp

<p>Nanosized mineral particles and organic matter (<100 nm) ,as well as their associations, belong to the most important ingredients for the formation of the soil aggregate structure being a hierarchically organized system. Colloids (< 220 nm) including nanoparticles can be occluded as primary building units of soil aggregates. Nevertheless, a large proportion of these colloids is mobile and presents in the solution phase (as “free”) within the soil matrix. However, the differences between “free” and occluded colloids remain unclear.</p><p>Here, both occluded and free colloids were isolated from soil samples of an arable field with different clay contents (19% and 34%) using wet sieving and centrifugation. The release of occluded colloids from soil macroaggregates (>250 µm) was carried out with ultrasonic treatment at 1000 J mL<sup>-1</sup>. The free and occluded colloidal fractions were then characterized for their size-resolved elemental composition using flow field-flow fractionation inductively coupled plasma mass spectrometry and organic carbon detector (FFF-ICP-MS/OCD). In addition, selected samples were also subjected to transmission electron microscopy as well as pyrolysis field ionization mass spectrometry (Py-FIMS).</p><p>Both, free and occluded colloids were composed of three size fractions: nanoparticles <20 nm, medium-sized nanoparticles (20 nm–60 nm), and, fine colloids (60 nm–220 nm). The fine colloid fraction was the dominant size fraction in both free and occluded colloids, which mainly consist of organic carbon, Al, Si, and Fe, probably present as phyllosilicates and associations of Fe- and Al- (hydr)oxides and organic matter. However, the organic matter contents for all three size fractions were higher for the occluded colloids than for the free ones. The role of OM concentration and composition in these colloids will be discussed in the paper.</p>


2018 ◽  
Author(s):  
Yinghui Wang ◽  
Robert G. M. Spencer ◽  
David Podgorski ◽  
Anne Kellerman ◽  
Harunur Rashid ◽  
...  

Abstract. The Qinghai-Tibetan Plateau (QTP) accounts for approximately 70 % of global alpine permafrost and is an area sensitive to climate change. The thawing and mobilization of ice and organic carbon-rich permafrost impact hydrologic conditions and biogeochemical processes on the QTP. Despite numerous studies of Arctic permafrost, there are no reports to date for the molecular-level in-stream processing of permafrost-derived dissolved organic matter (DOM) on the QTP. In this study, we examine temporal and spatial changes of chemical composition of DOM and 14C age of dissolved organic carbon (DOC) along an alpine stream (3850–3207 m above sea level) by Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS), accelerator mass spectrometry (AMS) and UV-visible spectroscopy. Compared to downstream sites, the DOM at the headstream exhibited older radiocarbon (14C-DOC) age, higher mean molecular weight, higher aromaticity and fewer polyunsaturated components. At the molecular level, 6409 and 1345 formulas were identified as unique to the active layer (AL) leachate and permafrost layer (PL) leachate, respectively. Comparing permafrost leachates to the downstream site, 59 % of AL-specific formulas and 90 % of PL-specific formulas were degraded, likely a result of rapid instream degradation of permafrost-derived DOM. From peak discharge in the summer to low flow in late autumn, the DOC concentration at the headstream site decreased from 13.9 to 10.2 mg/L, while the 14C-DOC age increased from 745 to 1560 years before present (BP), reflecting an increase in relative contribution of deep permafrost carbon due to the effect of changing hydrological conditions over the course of the summer on DOM source (AL vs. PL). Our study thus demonstrates that hydrological conditions impact the mobilization of permafrost carbon in an alpine fluvial network, the signature of which is quickly lost through in-stream metabolism.


2015 ◽  
Author(s):  
Andrew Decker Steen ◽  
Lauren N. M. Quigley ◽  
Alison Buchan

The "priming effect", in which addition of labile substances changes the remineralization rate of recalcitrant organic matter, has been intensively studied in soils, but is less well-documented in aquatic systems. We investigated the extent to which additions of nutrients or labile organic carbon could influence remineralization rates of 14C-labeled, microbially-degraded, phytoplankton-derived organic matter (OM) in microcosms inoculated with microbial communities drawn from Groves Creek Estuary in coastal Georgia, USA. We found that amendment with labile protein plus phosphorus increased remineralization rates of degraded, phytoplankton-derived OM by up to 100%, whereas acetate slightly decreased remineralization rates relative to an unamended control. Addition of ammonium and phosphate induced a smaller effect, whereas addition of ammonium alone had no effect. Counterintuitively, alkaline phosphatase activities increased in response to the addition of protein under P-replete conditions, indicating that production of enzymes unrelated to the labile priming compound may be a mechanism for the priming effect. The observed priming effect was transient: after 36 days of incubation roughly the same quantity of organic carbon had been mineralized in all treatments including no-addition controls. This timescale is on the order of the typical hydrologic residence times of well-flushed estuaries suggesting that priming in estuaries has the potential to influence whether OC is remineralized in situ or exported to the coastal ocean.


2016 ◽  
Author(s):  
Arístide Márquez ◽  
Gregorio Martínez ◽  
Julio Figuera ◽  
Ivis Fermín ◽  
William James Senior ◽  
...  

This paper reports the geochemical characteristics and environmental conditions of Cuchivero river sediments in Venezuela, depending on particle size, organic matter, organic carbon, nitrogen and total phosphorus, carbonates and heavy metals. The granulometry was typified by a predominance of sands with low organic matter (0.52 to 0.87%), organic carbon (0.06 to 0.09%) and carbonates content (0.54 to 2.61%) as well as high values of total nitrogen (602-985 mg / kg). The poor correlation between nitrogen, phosphorus and organic matter, suggests presence of nitrogen and total phosphorus of allochthonous origin and no Redfield organic matter. The average heavy metals in mg/kg, showed a descending concentration gradient, Fe (410)> Mn (63.14)> Zn (9.01)> Ni (3.38)> (2.21Cu)> Cr (2.09)> Co (1.13)> Cd (0.21) > Pb (0.07) mg / kg, with an association to the sands and carbonates, suggesting lithogenic origin. From the environmental point of view, there is no evidence of anthropogenic impact, as reflected by levels of organic matter and heavy metals which are below of the permissible values.


1981 ◽  
Vol 32 (2) ◽  
pp. 245 ◽  
Author(s):  
DJW Moriarty ◽  
MC Barclay

The food of seven species of penaeid prawns from the Gulf of Carpentaria consists predominantly of Foraminifera, small molluscs, crustaceans and polychaetes. Measurements of organic and inorganic carbon, organic nitrogen and bacterial biomass were made. Foregut contents of adult prawns contained between 72 and 223 mg organic carbon/g dry wt. Protein constituted between 43 and 64% of the organic matter. Approximate assimilation efficiencies of food in prawns caught in the gulf, determined for four species, varied from 48 to 77% of organic carbon and from 42 to 77% of organic nitrogen. The food of juvenile Penaeus merguiensis was examined for two growing seasons. In the 1976-1977 season the foregut contents contained a mean of 41 mg organic nitrogen /g dry wt and 181 mg organic carbon /g dry wt. In the 1977-1978 season, significantly lower proportions of organic nitrogen and carbon were eaten, viz, 21 mg organic nitrogenlg dry wt and 101 mg organic carbon /g dry wt. Improved assay procedures for muramic acid have shown that bacteria are less important in the food of prawns than previously reported. Bacteria constituted less than 2% of the organic matter in the adults of all species, but in many juvenile P. merguiensis bacteria were more important, constituting up to 14% of organic matter.


2020 ◽  
Author(s):  
Julia Gebert ◽  
Florian Zander

<p>Under anaerobic conditions, degradation of organic matter in river sediments leads to gas formation, with organic carbon being released mainly as CH<sub>4</sub> and CO<sub>2</sub>. Gas bubbles reduce sediment density, viscosity and shear strength, impede sonic depth finding and are suspected to affect the sediments’ rheological properties. Moreover, methane (CH<sub>4</sub>) is a potent greenhouse gas with a global warming potential (GWP<sub>100</sub>) of 28-36. Therefore, the climate impact may vary greatly depending on the way sediments are managed (for example, type and frequency of dredging and relocation in the water body or treatment on land). The objective of this paper is therefore to quantify the time-dependent stability, or inversely, the lability of sediment organic matter (SOM) as a basis for prediction of effects on sediment mechanical properties and on the release of greenhouse gases.</p><p>Within two years, over 200 samples of predominantly fine-grained sediment were collected from nine locations within a 30 km transect through the Port of Hamburg. All samples were, amongst other analyses, subjected to long-term (> 250 days) aerobic and anaerobic incubation for measurement of SOM degradation, yielding a comprehensive data set on the time-dependent change in degradation rates and the corresponding size of differently degradable SOM pools. SOM degradability exhibited a pronounced spatial variability with an approximately tenfold higher anaerobic and a roughly fivefold higher aerobic degradability of upstream SOM compared to downstream SOM. Lower δ<sup>13</sup>C values, higher DNA concentrations and a higher share of organic carbon in the light density fraction as well as elevated chlorophyll concentrations in the water phase support the hypothesis of increased biological sources of SOM at upstream locations and increased SOM degradability in shallow compared to deep layers (Zander et al., 2020).</p><p>First statistical and time series analyses indicate that</p><ul><li>Long-term SOM lability appears to be predictable from short-term measurements.</li> <li>The relationship between short-term and long-term SOM degradation is site-specific and also differs for layers of different age (depth). This supports the above-mentioned variability between sites regarding the size of differently degradable carbon pools, as well as for the depth profile at any one site.</li> <li>The relevance of the available electron acceptors (redox conditions) for SOM degradation, i.e. the ratio between carbon release under aerobic and anaerobic conditions, differs less by site but more so by layers of different age (depth). This is plausible as especially the top layers are exposed to more variability in redox conditions than the deeper layers that are always under reducing conditions.</li> </ul><p>Zander, F., Heimovaara, T., Gebert, J. (2020): Spatial variability of organic matter degradability in tidal Elbe sediments. Journal of Soils and Sediments, accepted for publication.</p>


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