Organic Carbon In Marine Sediments Research Articles

Unexpected carbon utilization activity of sulfate-reducing microorganisms in temperate and permanently cold marine sediments.

Significant amounts of organic carbon in marine sediments are degraded, coupled with sulfate reduction. However, the actual carbon and energy sources used in situ have not been assigned to each group of diverse sulfate-reducing microorganisms (SRM) owing to the microbial and environmental complexity in sediments. Here, we probed microbial activity in temperate and permanently cold marine sediments by using potential SRM substrates, organic fermentation products at very low concentrations (15-30μM), with RNA-based stable isotope probing. Unexpectedly, SRM were involved only to a minor degree in organic fermentation product mineralization, whereas metal-reducing microbes were dominant. Contrastingly, distinct SRM strongly assimilated 13C-DIC (dissolved inorganic carbon) with H2 as the electron donor. Our study suggests that canonical SRM prefer autotrophic lifestyle, with hydrogen as the electron donor, while metal-reducing microorganisms are involved in heterotrophic organic matter turnover, and thus regulate carbon fluxes in an unexpected way in marine sediments.

Selective Sorting and Degradation of Permafrost Organic Matter in the Nearshore Zone of Herschel Island (Yukon, Canada)

AbstractErosion of permafrost coasts due to climate warming releases large quantities of organic carbon (OC) into the Arctic Ocean. While burial of permafrost OC in marine sediments potentially limits degradation, resuspension of sediments in the nearshore zone potentially enhances degradation and greenhouse gas production, adding to the “permafrost carbon feedback.” Recent studies, focusing on bulk sediments, suggest that permafrost OC derived from coastal erosion is predominantly deposited close to shore. However, bulk approaches disregard sorting processes in the coastal zone, which strongly influence the OC distribution and fate. We studied soils and sediments along a transect from the fast‐eroding shoreline of Herschel Island—Qikiqtaruk (Yukon, Canada) to a depositional basin offshore. Sample material was fractionated by density (1.8 g cm−3) and size (63 μm), separating loose OC from mineral‐associated OC. Each fraction was analyzed for element content (TOC, TN), carbon isotopes (δ13C, Δ14C), molecular biomarkers (n‐alkanes, n‐alkanoic acids, lignin phenols, cutin acids), and mineral surface area. The OC partitioning between fractions changes considerably along the transect, highlighting the importance of hydrodynamic sorting in the nearshore zone. Additionally, OC and biomarker loadings decrease along the land‐ocean transect, indicating significant loss of OC during transport. However, molecular proxies for degradation show contrasting trends, suggesting that OC losses are not always well reflected in its degradation state. This study, using fraction partitioning that crosses land‐ocean boundaries in a way not done before, aids to disentangle sorting processes from degradation patterns, and provides quantitative insight into losses of thawed and eroded permafrost OC.

Influence of mineralized organic carbon in marine sediments on ecological heavy metal risk: Bohai Bay case study

The organic matter in sediments can mineralize over time, which impacts the morphology of the heavy metals therein, which in turn affects the assessment of the risks posed by heavy metals. We used the sediments of Bohai Bay as the study object and analyzed the effects of different organic carbon mineralization levels on the concentrations of heavy metals (Cr, Pb, Cu, Zn, and Cd) using water extraction and potassium permanganate oxidation. The mean concentrations of Cd, Pb, Cu, and Zn in Bohai Bay were within the limits recommended by the World Health Organization. The proportions of the active and inert organic carbon fractions were 61.72% and 32.94%, respectively. Organic carbon mineralization most strongly impacted Cd and Pb levels, with releases accounting for 47.92% and 25.75%, respectively, of the oxidizable fractions. The release of all heavy metals, except for Cr, increased with increases in organic carbon mineralization, and heavy metals were released at a maximum rate of 12.94% when the organic carbon was highly mineralized, whereas Cr was released at a maximum of 0.023% during the first stage of organic carbon mineralization. In terms of spatial distribution, the concentration of mineralizable organic carbon in the sediments of the estuaries was substantially higher than that in other marine areas. Estuary sediments were more easily affected by organic carbon mineralization; therefore, the heavy metals in the oxidizable fraction of the estuarine region were more easily transformed into unstable heavy metal forms, posing high risk levels. Therefore, this study highlights the effects of organic carbon mineralization on heavy metal morphology and stability, when evaluating the ecological risk of heavy metals in marine sediments.

The Modern Ocean Sediment Archive and Inventory of Carbon (MOSAIC): version 2.0

Abstract. Marine sediments play a crucial role in the global carbon cycle by acting as the ultimate sink of both terrestrial and marine organic carbon. To understand the spatiotemporal variability in the content, sources, and dynamics of organic carbon in marine sediments, a curated and harmonized database of organic carbon and associated parameters is needed, which has prompted the development of the Modern Ocean Sediment Archive and Inventory of Carbon (MOSAIC) database (http://mosaic.ethz.ch/, last access: 26 July 2023; https://doi.org/10.5281/zenodo.8322094, Paradis, 2023; https://doi.org/10.5168/mosaic019.1, Van der Voort et al., 2019​​​​​​​). MOSAIC version 2.0 has expanded the spatiotemporal coverage of the original database by >400 % and now holds data from more than 21 000 individual sediment cores from different continental margins on a global scale. Additional variables have also been incorporated into MOSAIC v.2.0 that are crucial to interpret the quantity, origin, and age of organic carbon in marine sediments globally. Sedimentological parameters (e.g. grain size fractions and mineral surface area) help understand the effect of hydrodynamic sorting and mineral protection on the distribution of organic carbon, while molecular biomarker signatures (e.g. lignin phenols, fatty acids, and alkanes) can help constrain the specific origin of organic matter. MOSAIC v.2.0 also stores data on specific sediment and molecular fractions, which provide further insight into the processes that affect the degradation and ageing of organic carbon in marine sediments. Data included within MOSAIC are continuously expanding, and version control will allow users to benefit from updated versions while ensuring reproducibility of their findings.

The effect of iron on the preservation of organic carbon in marine sediments and its implications for carbon sequestration

The effect of iron on the preservation of organic carbon in marine sediments and its implications for carbon sequestration

The Global Turbidity Current Pump and Its Implications for Organic Carbon Cycling.

Submarine turbidity currents form the largest sediment accumulations on Earth, raising the question of their role in global carbon cycles. It was previously inferred that terrestrial organic carbon was primarily incinerated on shelves and that most turbidity current systems are presently inactive. Turbidity currents were thus not considered in global carbon cycles, and the burial efficiency of global terrestrial organic carbon was considered low to moderate (∼10-44%). However, recent work has shown that burial of terrestrial organic carbon by turbidity currents is highly efficient (>60-100%) in a range of settings and that flows occur more frequently than once thought, although they were far more active at sea-level lowstands. This leads to revised global estimates for mass flux (∼62-90 Mt C/year) and burial efficiency (∼31-45%) of terrestrial organic carbon in marine sediments. Greatly increased burial fluxes during sea-level lowstands are also likely underestimated; thus, organic carbon cycling by turbidity currents could play a role in long-term changes in atmospheric CO2 and climate.

Compositions and sources of sedimentary organic carbon on the tropical epicontinental sea

The deposition of fluvially derived terrestrial organic carbon (OC) together with marine OC in marine sediments has important implications for the global carbon cycle. However, dispersal extent and fates of terrestrial soil and petrogenic OC on the continental shelf have remained unclear and debated. Here, we present OC compositions and mineral properties of marine sediments from the Gulf of Thailand and the adjacent Mekong shelf, as well as river sediments from continents surrounding them in order to determine the provenance of sedimentary OC in this tropical epicontinental sea. We find that stable carbon isotope composition (δ13C) and radiocarbon activity (Δ14C) of sedimentary OC fall between those of marine OC and of river sediments, mainly composed of C3 plant-dominated pre-aged soil and petrogenic OC. Mixing model reveals that the OC in river sediments is predominantly sourced from pre-aged deep soils, accounting for 73 ± 5%, with the remaining consisting of modern surface soil (25 ± 6%) and bedrock (2 ± 1%). The sedimentary OC on the shelf is primarily derived from marine OC, accounting for 65 ± 15%, with terrestrial soil OC and petrogenic OC contributing 24 ± 14% and 10 ± 5%, respectively. The sources, degradation, and aging of OC and mineral surface area determine the spatial pattern of sedimentary OC compositions in the Gulf of Thailand and the Mekong shelf. The contents of marine, soil, and petrogenic OC decrease with increasing distance offshore, consistent with changes in spatial patterns of sedimentation rate of terrestrial materials and of marine primary production in the overlying water column. Extensive degradation of terrestrial OC and extremely low OC burial rate in this tropical epicontinental sea suggest a minor role on OC sequestration in marine sediments, but an important CO2 source to the atmosphere in the context of the global carbon cycle.

Temporal variation of mineralization rates and its influence on carbon storage over the last 50 years in Bohai Bay, China

Recorded information on marine sediments is affected by mineralization. In this study, we collected sediment samples from Bohai Bay, where human interference is typically high. Overall, the CO2 fluxes in the columnar sediments decreased with increasing depth. The change in constants revealed a “C-curve” in which the mineralization rate first decreased significantly (i.e., from the 2020s to the 1980s) and subsequently increased slowly (i.e., from the 1980s to 1965). This may be explained by the fact that sediments from the 1980s–2020s were markedly influenced by the sedimentation rate, whereas sediments from the 1960s–1980s were predominantly influenced by microbial action. The loss of organic carbon due to mineralization accounted for approximately 15–20 % of the initial total organic carbon; therefore, when performing an inversion of the historical environment change using information derived from organic carbon in marine sediments, the influence of mineralization on this information should be fully considered.

Transfer efficiency of organic carbon in marine sediments

Quantifying the organic carbon (OC) sink in marine sediments is crucial for assessing how the marine carbon cycle regulates Earth’s climate. However, burial efficiency (BE) – the commonly-used metric reporting the percentage of OC deposited on the seafloor that becomes buried (beyond an arbitrary and often unspecified reference depth) – is loosely defined, misleading, and inconsistent. Here, we use a global diagenetic model to highlight orders-of-magnitude differences in sediment ages at fixed sub-seafloor depths (and vice-versa), and vastly different BE’s depending on sediment depth or age horizons used to calculate BE. We propose using transfer efficiencies (Teff’s) for quantifying sediment OC burial: Teff is numerically equivalent to BE but requires precise specification of spatial or temporal references, and emphasizes that OC degradation continues beyond these horizons. Ultimately, quantifying OC burial with precise sediment-depth and sediment-age-resolved metrics will enable a more consistent and transferable assessment of OC fluxes through the Earth system.

Differentiating the Causes of Aged Organic Carbon in Marine Sediments

AbstractAged organic carbon (OC) is widely observed in surficial sediments deposited on continental margins, resulting from several factors including old OC input and sedimentological processes. While the supply of old OC to marine sediments has been examined and quantified in a range of continent margin settings, there have been few attempts to constrain the extent to which hydrodynamic processes, specifically lateral transport, contribute to the old age of sedimentary OC. Here, we propose a mathematical index, bAgedOC, to differentiate the causes of sedimentary aged OC, and apply this approach to two typical sediment transport pathways that follow the supply and dispersal of terrestrial OC in the marine environment, and further extrapolate it to submarine canyon, Arctic and deep‐sea environments. The index, representing a modification of a widely used quantitative method, provides a novel approach to distinguish the contribution of lateral transport to the pre‐depositional aging of OC in the oceanic region.

Sounding Out the Carbon: The Potential of Acoustic Backscatter Data to Yield Improved Spatial Predictions of Organic Carbon in Marine Sediments

Marine sediments hold vast stores of organic carbon (OC). Techniques to spatially map sedimentary OC must develop to form the basis of seabed management tools that consider carbon-rich sediments. While the natural burial of carbon (C) provides a climate regulation service, the disturbance of buried C could present a significant positive feedback mechanism to atmospheric greenhouse gas concentrations. We present a regional Scottish case study that explores the suitability of integrating archived seafloor acoustic data (i.e., multibeam echosounder bathymetry and backscatter) with physical samples toward improved spatial mapping of surface OC in a dynamic coastal environment. Acoustic backscatter is a proxy for seabed sediments and can be collected over extensive areas at high resolutions. Sediment type is also an important predictor of OC. We test the potential of backscatter as a proxy for OC which may prove useful in the absence of exhaustive sediment data. Overall, although statistically significant, correlations between the variables OC, sediment type, and backscatter are relatively weak, likely reflecting a combination of limited and asynchronous data, sediment mobility over time, and complex environmental processing of OC in shelf sediments. We estimate linear mixed models to predict OC using backscatter and Folk sediment type as covariates. Our results show that incorporating backscatter in the model improves the precision of OC predictions by 14%. Backscatter discriminates between coarse and fine sediments, and therefore low and high OC regimes; however, was not able to discriminate amongst finer sediments. Although sediment type is a stronger predictor of OC, these data are available at a much lower spatial resolution and do not account for fine-scale variability. The resulting maps display varying spatial distributions of OC reflecting the different scales of the predictor variables, demonstrating a need for further methodological development. Backscatter shows considerable promise as a high-resolution predictor variable to improve the precision of surface OC maps, or to reduce the number of OC measurements required to achieve a specified precision. Applications of such maps have potential in improved C-stock estimates and the design of conservation and management strategies that consider marine sediments as valuable C stores.

A chemical weathering control on the delivery of particulate iron to the continental shelf

The delivery of potentially reactive iron minerals to the marine environment exerts a major control on ocean and marine sediment biogeochemistry, including the preservation and burial of organic carbon. One aspect of the global iron cycle that has received little attention concerns the phase partitioning of iron in highly chemically-weathered sediments from (sub)tropical mountainous regions, where the sediment is commonly deposited directly onto adjacent continental margins. Here, we report the phase partitioning of particulate iron in surface seafloor sediments deposited from oxic bottom waters along the east coast of China, including the Bohai Sea, Yellow Sea and East China Sea, in addition to the continental shelf region adjacent to the (sub)tropical mountainous island of Hainan in the northern South China Sea. We document highly reactive (FeHR) to total iron (FeT) ratios for the Bohai Sea, Yellow Sea and East China Sea that are typical of global marine sediments deposited under oxic water column conditions. By contrast, FeHR/FeT ratios in Hainan offshore sediments are significantly elevated above normal oxic marine sediments. These Hainan offshore sediments display a strong positive correlation between FeHR/FeT ratios and the chemical index of alteration (CIA) weathering proxy, suggesting that the Fe speciation systematics are controlled by the intensity of chemical weathering. This observation is supported by additional geochemical data and Nd isotope analyses, which suggest a common source lithology for all the studied regions. The Hainan sediments thus document a specific scenario, whereby highly chemically weathered sediments from the mountainous Hainan region bypass the inner shore settings that commonly disproportionately trap Fe (oxyhydr)oxide minerals, depositing high concentrations of FeHR on the adjacent continental margin. Such enrichments likely aid in the preservation of organic carbon in marine sediments, suggesting that organic carbon preservation and burial may be enhanced by elevated FeHR in such settings. We also establish a set of essential criteria for potential recognition of chemical weathering-induced enrichments in FeHR/FeT ratios in ancient marine sediments.

Using Radiocarbon to Assess the Abundance, Distribution, and Nature of Labile Organic Carbon in Marine Sediments

AbstractPositive 14C gradients have recently been observed within the surface mixed layer of several continental‐margin sediments. The best explanation for these positive 14C gradients is the occurrence and rapid degradation of labile organic carbon (LOC) in the upper 5–10 cm of the seabed. Based on a two‐component model for sedimentary organic matter (i.e., a planktonic labile component and an older refractory component), bulk 14Corg data were used to determine the abundances of LOC within the surface mixed layers of three cores from the West Antarctic Peninsula (WAP) shelf and one core from San Clemente Basin (California Borderland). LOC contents in surface samples from the four stations varied from 0.5 to 1.1 mg/cm3, comprising 20% (San Clemente Basin) to 80% (WAP, Sta. G) of the total organic carbon. By incorporating a steady state diagenetic model and particle‐mixing bioturbation coefficients, the LOC profiles were used to determine LOC turnover times (LOC τ) and LOC e‐folding depths. The LOC τ values for the West Antarctic Peninsula sediments varied from 0.09 to 0.59 years, whereas the LOC τ value from the San Clemente Basin core was 63 years. The LOC e‐folding depths for the WAP stations varied from 0.8 to 3.4 cm, in contrast to the LOC e‐folding depth in San Clemente Basin, which was 4.0 cm. LOC characteristics from the four cores examined in this study were compared to LOC data in the literature as a means of substantiating the overall 14Corg‐based approach and justifying model assumptions.

Nearshore Zone Dynamics Determine Pathway of Organic Carbon From Eroding Permafrost Coasts

Collapse of permafrost coasts delivers large quantities of particulate organic carbon (POC) to Arctic coastal areas. With rapidly changing environmental conditions, sediment and organic carbon (OC) mobilization and transport pathways are also changing. Here, we assess the sources and sinks of POC in the highly dynamic nearshore zone of Herschel Island‐Qikiqtaruk (Yukon, Canada). Our results show that POC concentrations sharply decrease, from 15.9 to 0.3 mg L−1, within the first 100–300 m offshore. Simultaneously, radiocarbon ages of POC drop from 16,400 to 3,600 14C years, indicating rapid settling of old permafrost POC to underlying sediments. This suggests that permafrost OC is, apart from a very narrow resuspension zone (<5 m water depth), predominantly deposited in nearshore sediments. While long‐term storage of permafrost OC in marine sediments potentially limits biodegradation and its subsequent release as greenhouse gas, resuspension of fine‐grained, OC‐rich sediments in the nearshore zone potentially enhances OC turnover.

Organic carbon and microbial activity in marine sediments on a global scale throughout the Quaternary

Microbial degradation of organic carbon in marine sediments is a key driver of global element cycles on multiple time scales. However, it is not known to what depth microorganisms alter organic carbon in marine sediments or how microbial rates of organic carbon processing change with depth, and thus time since burial, on a global scale. To better understand the connection between the dynamic carbon cycle and life’s limits in the deep subsurface, we have combined a number of global data sets with a reaction transport model (RTM) describing first, organic carbon degradation in marine sediments deposited throughout the Quaternary Period and second, a bioenergetic model for microbial activity. The RTM is applied globally, recognizing three distinct depositional environments – continental shelf, margin and abyssal zones. The results include the masses of particulate organic carbon, POC, stored in three sediment-depth layers: bioturbated Holocene (1.7 × 1017 g C), non-bioturbated Holocene (2.5 × 1018 g C) and Pleistocene (1.4 × 1020 g C) sediments. The global depth-integrated rates of POC degradation have been determined to be 1.3 × 1015, 1.3 × 1014 and 3.0 × 1014 g C yr−1 for the same three layers, respectively. A number of maps depicting the distribution of POC, as well as the fraction that has been degraded have also been generated. Using POC degradation as a proxy for microbial catabolic activity, total heterotrophic processing of POC throughout the Quaternary is estimated to be between 10−11 and 10−6 g C cm−3 yr−1, depending on the time since deposition and location. Bioenergetic modeling reveals that laboratory-determined microbial maintenance powers are poor predictors of sediment biomass concentration, but that cell concentrations in marine sediments can be accurately predicted by combining bioenergetic models with the rates of POC degradation determined in this study. Our model can be used to quantitatively describe both the carbon cycle and microbial activity on a global scale for marine sediments less than 2.59 million years old.

Efficient preservation of young terrestrial organic carbon in sandy turbidity-current deposits

Abstract Burial of terrestrial biospheric particulate organic carbon in marine sediments removes CO2 from the atmosphere, regulating climate over geologic time scales. Rivers deliver terrestrial organic carbon to the sea, while turbidity currents transport river sediment further offshore. Previous studies have suggested that most organic carbon resides in muddy marine sediment. However, turbidity currents can carry a significant component of coarser sediment, which is commonly assumed to be organic carbon poor. Here, using data from a Canadian fjord, we show that young woody debris can be rapidly buried in sandy layers of turbidity current deposits (turbidites). These layers have organic carbon contents 10× higher than the overlying mud layer, and overall, woody debris makes up &amp;gt;70% of the organic carbon preserved in the deposits. Burial of woody debris in sands overlain by mud caps reduces their exposure to oxygen, increasing organic carbon burial efficiency. Sandy turbidity current channels are common in fjords and the deep sea; hence we suggest that previous global organic carbon burial budgets may have been underestimated.

Reactivity of Iron Minerals in the Seabed Toward Microbial Reduction – A Comparison of Different Extraction Techniques

Dissimilatory iron reduction and sulfate reduction are the most important processes for anaerobic mineralization of organic carbon in marine sediments. The thermodynamics and kinetics of microbial Fe(III) reduction depend on the characteristics of the Fe(III) minerals, which influence the potential of Fe(III)-reducers to compete with sulfate-reducers for common organic substrates. In the present study, we tested different methods to quantify and characterize microbially reducible Fe(III) in sediments from a transect in Kongsfjorden, Svalbard, using different standard sequential endpoint extractions and time-course extractions with either ascorbate or a Fe(III)-reducing microbial culture. Similar trends of increasing ‘reactive Fe’ content of the sediment along the fjord transect were found using the different extraction methods. However, the total amount of ‘reactive Fe’ extracted differed between the methods, due to different Fe dissolution mechanisms and different targeted Fe fractions. Time-course extractions additionally provided information on the reactivity and heterogeneity of the extracted Fe(III) minerals, which also impact the favorability for microbial reduction. Our results show which fractions of the existing Fe extraction protocols should be considered ‘reactive’ in the sense of being favorable for microbial Fe(III) reduction, which is important in studies on early diagenesis in marine sediments.

An improved method for quantitatively measuring the sequences of total organic carbon and black carbon in marine sediment cores

Understanding global carbon cycle is critical to uncover the mechanisms of global warming and remediate its adverse effects on human activities. Organic carbon in marine sediments is an indispensable part of the global carbon reservoir in global carbon cycling. Evaluating such a reservoir calls for quantitative studies of marine carbon burial, which closely depend on quantifying total organic carbon and black carbon in marine sediment cores and subsequently on obtaining their high-resolution temporal sequences. However, the conventional methods for detecting the contents of total organic carbon or black carbon cannot resolve the following specific difficulties, i.e., (1) a very limited amount of each subsample versus the diverse analytical items, (2) a low and fluctuating recovery rate of total organic carbon or black carbon versus the reproducibility of carbon data, and (3) a large number of subsamples versus the rapid batch measurements. In this work, (i) adopting the customized disposable ceramic crucibles with the microporecontrolled ability, (ii) developing self-made or customized facilities for the procedures of acidification and chemothermal oxidization, and (iii) optimizing procedures and carbon-sulfur analyzer, we have built a novel Wang-Xu-Yuan method (the WXY method) for measuring the contents of total organic carbon or black carbon in marine sediment cores, which includes the procedures of pretreatment, weighing, acidification, chemothermal oxidation and quantification; and can fully meet the requirements of establishing their highresolution temporal sequences, whatever in the recovery, experimental efficiency, accuracy and reliability of the measurements, and homogeneity of samples. In particular, the usage of disposable ceramic crucibles leads to evidently simplify the experimental scenario, which further results in the very high recovery rates for total organic carbon and black carbon. This new technique may provide a significant support for revealing the mechanism of carbon burial and evaluating the capacity of marine carbon accumulation and sequestration.

Evolution of biomolecular loadings along a major river system

Understanding the transport history and fate of organic carbon (OC) within river systems is crucial in order to constrain the dynamics and significance of land–ocean interactions as a component of the global carbon cycle. Fluvial export and burial of terrestrial OC in marine sediments influences atmospheric CO2 over a range of timescales, while river-dominated sedimentary sequences can provide valuable archives of paleoenvironmental information. While there is abundant evidence that the association of organic matter (OM) with minerals exerts an important influence on its stability as well as hydrodynamic behavior in aquatic systems, there is a paucity of information on where such associations form and how they evolve during fluvial transport. Here, we track total organic carbon (TOC) and terrestrial biomarker concentrations (plant wax-derived long-chain fatty acids (FA), branched glycerol dialkyl glycerol tetraethers (brGDGTs) and lignin-derived phenols) in sediments collected along the entire course of the Danube River system in the context of sedimentological parameters. Mineral-specific surface area-normalized biomarker and TOC concentrations show a systematic decrease from the upper to the lower Danube basin. Changes in OM loading of the available mineral phase correspond to a net decrease of 70–80% of different biomolecular components. Ranges for biomarker loadings on Danube River sediments, corresponding to 0.4–1.5 μgFA/m2 for long-chain (n-C24–32) fatty acids and 17–71 ngbrGDGT/m2 for brGDGTs, are proposed as a benchmark for comparison with other systems. We propose that normalizing TOC as well as biomarker concentrations to mineral surface area provides valuable quantitative constraints on OM dynamics and organo-mineral interactions during fluvial transport from terrigenous source to oceanic sink.

Application of Portable Near-Infrared Spectrometer for Analysis of Organic Carbon in Marine Sediments

The performance of a portable near-infrared (NIR) spectrometer to determine organic carbon (OC) in marine sediments was evaluated. The NIR reflection spectra of 180 samples in the range 950 - 1650 nm were acquired using an ultra-compact spectrometer. NIR spectroscopy combined with the partial least squares (PLS) regression and Savitzky-Golay (SG) smoothing was successfully applied to rapid and reagent-free determination of OC. Using the PLS-SG model with 1nd order derivative, 2th polynomial and eleven smoothing points, the root-mean-square errors (RMSEPM) and correlation coefficients (RP,M) of prediction for modeling were 0.073% and 0.894, respectively, the root-mean-square errors (RMSEPV) and correlation coefficients (RP,V) of prediction for validation were 0.075% and 0.883, respectively. Results showed that the small portable NIR instrument achieved well prediction effect for the analysis of OC in marine sediments, which had advantages of rapid, easy to carry and operate suitable for large-scale applications to analyze marine sediments.