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Sample records for organic carbon determination

  1. Carbon Mineralizability Determines Interactive Effects on Mineralization of Pyrogenic Organic Matter and Soil Organic Carbon

    SciTech Connect

    Whitman, Thea L.; Zhu, Zihua; Lehmann, Johannes C.

    2014-10-31

    Soil organic carbon (SOC) is a critical and active pool in the global C cycle, and the addition of pyrogenic organic matter (PyOM) has been shown to change SOC cycling, increasing or decreasing mineralization rates (often referred to as priming). We adjusted the amount of easily mineralizable C in the soil, through 1-day and 6-month pre-incubations, and in PyOM made from maple wood at 350°C, through extraction. We investigated the impact of these adjustments on C mineralization interactions, excluding pH and nutrient effects and minimizing physical effects. We found short-term increases (+20-30%) in SOC mineralization with PyOM additions in the soil pre-incubated for 6 months. Over the longer term, both the 6-month and 1-day pre-incubated soils experienced net ~10% decreases in SOC mineralization with PyOM additions. This was possibly due to stabilization of SOC on PyOM surfaces, suggested by nanoscale secondary ion mass spectrometry. Additionally, the duration of pre-incubation affected priming interactions, indicating that there may be no optimal pre-incubation time for SOC mineralization studies. We show conclusively that relative mineralizability of SOC in relation to PyOM-24 C is an important determinant of the effect of PyOM additions on SOC mineralization.

  2. TOTAL ORGANIC CARBON DETERMINATIONS IN NATURAL AND CONTAMINATED AQUIFER MATERIALS

    EPA Science Inventory

    Quantifying the total organic carbon (TOC) content of soils and aquifer materials is essential for understanding subsurface chemistry during environmental site characterization. ontaminant fate and transport, microbial ecology, and effective treatment methodology are all influenc...

  3. Arterial Blood Carbonic Acid Inversely Determines Lactic and Organic Acids

    PubMed Central

    Aiken, Christopher Geoffrey Alexander

    2013-01-01

    Objective: To establish that arterial blood carbonic acid varies inversely with lactic acid in accordance with bicarbonate exchanging for lactate across cell membranes through the anion exchange mechanism to maintain the Gibbs-Donnan equilibrium. Study Design: Over 5 years, lactate was measured on all blood gases taken from neonatal admissions, as well as organic acid whenever electrolytes were required. Results: Arterial blood gases from 63 infants given high calcium TPN were analyzed. Twenty two needed continuous positive airways pressure (CPAP) only and 31 intermittent positive pressure ventilation (IPPV) and surfactant followed by CPAP to treat respiratory distress syndrome in 51 and meconium aspiration syndrome in 2. All survived and were free of infection. Excluded gases were those with high and falling lactate soon after delivery representing perinatal asphyxia, and those on dexamethasone. Strong inverse relations between carbonic and lactic acids were found at all gestational ages and, independent of glomerular filtration, between carbonic and organic acids. Lactate (mmol/L) = 62.53 X PCO2 -0.96(mmHg) r2 0.315, n 1232, p <0.001. Sixty divided by PCO2 is a convenient measure of physiological lactate at any given PCO2. In the first week, 9.13 ± 2.57% of arterial gases from infants on IPPV had lactates above 120/PCO2, significantly more than 4.74 ± 2.73% on CPAP (p<0.05) and 2.47 ± 2.39% on no support. Conclusion: Changes in arterial blood carbonic acid cause immediate inverse changes in lactic acid, because their anions interchange across cell membranes according to the Gibbs –Donnan equilibrium. Increasing PCO2 from 40 to 120 mmHg decreased lactate from 1.5 mmol/L to 0.5 mmol/L, so that the sum of carbonic and lactic acids increased from 2.72 mmol/L to only 4.17 mmol/L. This helps explain the neuroprotective effect of hypercapnoea and highlights the importance of avoiding any degree of hypocapnoea in infants on IPPV. PMID:24392387

  4. Determining carbon-carbon connectivities in natural abundance organic powders using dipolar couplings.

    PubMed

    Dekhil, Myriam; Mollica, Giulia; Bonniot, Tristan Texier; Ziarelli, Fabio; Thureau, Pierre; Viel, Stéphane

    2016-06-30

    We present a solid-state NMR methodology capable of investigating the carbon skeleton of natural abundance organic powders. The methodology is based on the (13)C-(13)C dipolar coupling interaction and allows carbon-carbon connectivities to be unambiguously established for a wide range of organic solids. This methodology is particularly suitable for disordered solids, such as natural or synthetic macromolecules, which cannot be studied using conventional diffraction or NMR techniques. PMID:27319808

  5. Analytical determination of the aerosol organic mass-to-organic carbon ratio.

    PubMed

    El-Zanan, Hazem S; Zielinska, Barbara; Mazzoleni, Lynn R; Hansen, D Alan

    2009-01-01

    Particulate matter (PM) with an aerodynamic diameter < or = 2.5 microm (PM2.5) was collected daily (mid-July 1998 to the end of December 1999) over a 24-hr sampling period in a mixed light industrial-residential area in Atlanta, GA, to provide a subset of data for the Aerosol Research and Inhalation Epidemiology Study (ARIES). This study included the measurement of organic carbon (OC), elemental carbon (EC), and individual organic compounds. OC and EC average mean concentrations were 4.50 +/- 0.33 and 2.08 +/- 0.19 microg/m3, respectively. The ratio of organic matter mass (OM) to OC in PM2.5 aerosols in Atlanta was measured using three different approaches: (1) solvent extract residue gravimetric masses to individual OC concentrations of sequential apolar to polar solvent extracts (dichloromethane, acetone, and water); (2) mass balance of the PM2.5 measured gravimetric mass minus the mass concentrations of the inorganic/elemental constituents to the total OC concentration; and (3) polar organic compound speciation with the concentration weighted ratio to the total OC concentration. We found very good agreement between approach 1 and 2. The average OM/OC ratio calculated from the extract residue mass was 2.14 +/- 0.17. The average OM/OC ratio determined by mass balance was 2.16 +/- 0.43 for the whole period. The concentration weighted ratio calculated from the concentrations of polar organic compounds ranged between 1.55 and 1.72, which was likely a lower limit for the ratio because of the limited number of the polar organic compounds that can be quantified using gas chromatographic methods. We found seasonal differences with an OM/OC range of 1.77 in December 1999 to 2.39 in July 1999. These results suggest that the previously accepted value of 1.4 for the OM/OC ratio was too low even for urban locations during the winter months. Molecular-level speciation of the PM2.5-associated organic compounds showed that the concentrations of the molecular markers for wood

  6. Determining organic carbon distributions in soil particle size fractions as a precondition of lateral carbon transport modeling at large scales

    NASA Astrophysics Data System (ADS)

    Schindewolf, Marcus; Seher, Wiebke; Pfeffer, Eduard; Schultze, Nico; Amorim, Ricardo S. S.; Schmidt, Jürgen

    2016-04-01

    The erosional transport of organic carbon has an effect on the global carbon budget, however, it is uncertain, whether erosion is a sink or a source for carbon in the atmosphere. Continuous erosion leads to a massive loss of top soils including the loss of organic carbon historically accumulated in the soil humus fraction. The colluvial organic carbon could be protected from further degradation depending on the depth of the colluvial cover and local decomposing conditions. Another part of eroded soils and organic carbon will enter surface water bodies and might be transported over long distances. The selective nature of soil erosion results in a preferential transport of fine particles while less carbonic larger particles remain on site. Consequently organic carbon is enriched in the eroded sediment compared to the origin soil. As a precondition of process based lateral carbon flux modeling, carbon distribution on soil particle size fractions has to be known. In this regard the present study refers to the determination of organic carbon contents on soil particle size separates by a combined sieve-sedimentation method for different tropical and temperate soils Our results suggest high influences of parent material and climatic conditions on carbon distribution on soil particle separates. By applying these results in erosion modeling a test slope was simulated with the EROSION 2D simulation software covering certain land use and soil management scenarios referring to different rainfall events. These simulations allow first insights on carbon loss and depletion on sediment delivery areas as well as carbon gains and enrichments on deposition areas on the landscape scale and could be used as a step forward in landscape scaled carbon redistribution modeling.

  7. Determination of the organic aerosol mass to organic carbon ratio in IMPROVE samples.

    PubMed

    El-Zanan, Hazem S; Lowenthal, Douglas H; Zielinska, Barbara; Chow, Judith C; Kumar, Naresh

    2005-07-01

    The ratio of organic mass (OM) to organic carbon (OC) in PM(2.5) aerosols at US national parks in the IMPROVE network was estimated experimentally from solvent extraction of sample filters and from the difference between PM(2.5) mass and chemical constituents other than OC (mass balance) in IMPROVE samples from 1988 to 2003. Archived IMPROVE filters from five IMPROVE sites were extracted with dichloromethane (DCM), acetone and water. The extract residues were weighed to determine OM and analyzed for OC by thermal optical reflectance (TOR). On average, successive extracts of DCM, acetone, and water contained 64%, 21%, and 15%, respectively, of the extractable OC, respectively. On average, the non-blank-corrected recovery of the OC initially measured in these samples by TOR was 115+/-42%. OM/OC ratios from the combined DCM and acetone extracts averaged 1.92 and ranged from 1.58 at Indian Gardens, AZ in the Grand Canyon to 2.58 at Mount Rainier, WA. The average OM/OC ratio determined by mass balance was 2.07 across the IMPROVE network. The sensitivity of this ratio to assumptions concerning sulfate neutralization, water uptake by hygroscopic species, soil mass, and nitrate volatilization were evaluated. These results suggest that the value of 1.4 for the OM/OC ratio commonly used for mass and light extinction reconstruction in IMPROVE is too low. PMID:15950041

  8. DETERMINATION OF THE ORGANIC MASS TO ORGANIC CARBON RATIO IN IMPROVE SAMPLES. (R831086)

    EPA Science Inventory

    The ratio of organic mass (OM) to organic carbon (OC) in PM2.5 aerosols at US national parks in the IMPROVE network was estimated experimentally from solvent extraction of sample filters and from the difference between PM2.5 mass and chemical constituents...

  9. Determining the Carbon-Carbon Distance in an Organic Molecule with a Ruler

    ERIC Educational Resources Information Center

    Simoni, Jose A.; Tubino, Matthieu; Ricchi, Reinaldo Alberto, Jr.

    2004-01-01

    The procedure to estimate the carbon-carbon bond distance in the naphthalene molecule is described. The procedure is easily performed and can be done either at home or in the classroom, with the restriction that the mass of the naphthalene must be determined using an analytical or a precise balance.

  10. Determining soil organic carbon accretion vs sequestration using physicochemical fractionation and CQESTR simulation

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Accurate estimates of soil organic carbon (SOC) are needed to determine SOC changes resulting from agricultural management practices. The objectives of this study were to: (1) determine total SOC, and estimate contributions of light fraction C (LF-C) and resistant C (RC) to total SOC; and (2) simula...

  11. Determination of primary and secondary sources of organic acids and carbonaceous aerosols using stable carbon isotopes

    NASA Astrophysics Data System (ADS)

    Fisseha, Rebeka; Saurer, Matthias; Jäggi, Maya; Siegwolf, Rolf T. W.; Dommen, Josef; Szidat, Sönke; Samburova, Vera; Baltensperger, Urs

    Stable carbon isotope ratio ( δ13C) data can provide important information regarding the sources and the processing of atmospheric organic carbon species. Formic, acetic and oxalic acid were collected from Zurich city in August-September 2002 and March 2003 in the gas and aerosol phase, and the corresponding δ13C analysis was performed using a wet oxidation method followed by isotope ratio mass spectrometry. In August, the δ13C values of gas phase formic acid showed a significant correlation with ozone (coefficient of determination ( r2) = 0.63) due to the kinetic isotope effect (KIE). This indicates the presence of secondary sources (i.e. production of organic acids in the atmosphere) in addition to direct emission. In March, both gaseous formic and acetic acid exhibited similar δ13C values and did not show any correlation with ozone, indicating a predominantly primary origin. Even though oxalic acid is mainly produced by secondary processes, the δ13C value of particulate oxalic acid was not depleted and did not show any correlation with ozone, which may be due to the enrichment of 13C during the gas - aerosol partitioning. The concentrations and δ13C values of the different aerosol fractions (water soluble organic carbon, water insoluble organic carbon, carbonate and black carbon) collected during the same period were also determined. Water soluble organic carbon (WSOC) contributed about 60% to the total carbon and was enriched in 13C compared to other fractions indicating a possible effect of gas - aerosol partitioning on δ13C of carbonaceous aerosols. The carbonate fraction in general was very low (3% of the total carbon).

  12. Interlaboratory study of a method for determining nonvolatile organic carbon in aquifer materials

    USGS Publications Warehouse

    Caughey, M.E.; Barcelona, M.J.; Powell, R.M.; Cahill, R.A.; Gron, C.; Lawrenz, D.; Meschi, P.L.

    1995-01-01

    The organic carbon fraction in aquifer materials exerts a major influence on the subsurface mobilities of organic and organic-associated contaminants. The spatial distribution of total organic carbon (TOC) in aquifer materials must be determined before the transport of hydrophobic organic pollutants in aquifers can be modeled accurately. Previous interlaboratory studies showed that it is difficult to measure TOC concentrations 1%. We have tested a new analytical method designed to improve the accuracy and precision of nonvolatile TOC quantitation in geologic materials that also contain carbonate minerals. Four authentic aquifer materials and one NIST standard reference material were selected as test materials for a blind collaborative study. Nonvolatile TOC in these materials ranged from 0.05 to 1.4%, while TIC ranged from 0.46 to 12.6%. Sample replicates were digested with sulfurous acid, dried at 40??C, and then combusted at 950??C using LECO or UIC instruments. For the three test materials that contained >2% TIC, incomplete acidification resulted in a systematic positive bias of TOC values reported by five of the six laboratories that used the test method. Participants did not have enough time to become proficient with the new method before they analyzed the test materials. A seventh laboratory successfully used an alternative method that analyzed separate liquid and solid fractions of the acidified sample residues. ?? 1995 Springer-Verlag.

  13. Clay:organic-carbon and organic carbon as determinants of the soil physical properties: reassessment of the Complexed Organic Carbon concept

    NASA Astrophysics Data System (ADS)

    Matter, Adrien; Johannes, Alice; Boivin, Pascal

    2016-04-01

    Soil Organic Carbon (SOC) is well known to largely determine the soil physical properties and fertility. Total porosity, structural porosity, aeration, structural stability among others are reported to increase linearly with increasing SOC in most studies. Is there an optimal SOC content as target in soil management, or is there no limit in physical fertility improvement with SOC? Dexter et al. (2008) investigated the relation between clay:SOC ratio and the physical properties of soils from different databases. They observed that the R2 of the relation between SOC and the physical properties were maximized when considering the SOC fraction limited to a clay:SOC ratio of 10. They concluded that this fraction of the SOC was complexed, and that the additional SOC was not influencing the physical properties as strongly as the complexed one. In this study, we reassessed this approach, on a database of 180 undisturbed soil samples collected from cambiluvisols of the Swiss Plateau, on an area of 2400 km2, and from different soil uses. The physical properties were obtained with Shrinkage Analysis, which involved the parameters used in Dexter et al., 2008. We used the same method, but detected biases in the statistical approach, which was, therefore, adapted. We showed that the relation between the bulk density and SOC was changing with the score of visual evaluation of the structure (VESS) (Ball et al., 2007). Therefore, we also worked only on the "good" structures according to VESS. All shrinkage parameters were linearly correlated to SOC regardless of the clay:SOC ratio, with R2 ranging from 0.45 to 0.8. Contrarily to Dexter et al. (2008), we did not observed an optimum in the R2 of the relation when considering a SOC fraction based on the clay:SOC ratio. R2 was increasing until a Clay:SOC of about 7, where it reached, and kept, its maximum value. The land use factor was not significant. The major difference with the former study is that we worked on the same soil group

  14. Determination of organic milk authenticity using carbon and nitrogen natural isotopes.

    PubMed

    Chung, Ill-Min; Park, Inmyoung; Yoon, Jae-Yeon; Yang, Ye-Seul; Kim, Seung-Hyun

    2014-10-01

    Natural stable isotopes of carbon and nitrogen ((12)C, (13)C, (14)N, (15)N) have abundances unique to each living creature. Therefore, measurement of the stable isotope ratio of carbon and nitrogen (δ(13)C=(13)C/(12)C, δ(15)N=(15)N/(14)N) in milk provides a reliable method to determine organic milk (OM) authenticity. In the present study, the mean δ(13)C value of OM was higher than that of conventional milk (CM), whereas the mean δ(15)N value of OM was lower than that of CM; nonetheless both δ(13)C and δ(15)N values were statistically different for the OM and CM (P<0.05). Furthermore, the values of δ(13)C and δ(15)N were found to differ statistically with the collection date and the milk brand (P<0.05). The combination of δ(13)C and δ(15)N values was more effective than either value alone in distinguishing between OM and CM. The results of the present study, which is based on preliminary data from a limited sample size and sampling period, could be highly valuable and helpful for consumers, the food industry, and/or government regulatory agencies as it can prevent fraudulent labelling of organic food. Further studies include additional analyses of other milk brands and analyses over longer time periods in order to accurately determine OM authenticity using stable isotopes of carbon and nitrogen. PMID:24799230

  15. Determinants of soil organic carbon pools in oak stands in northeastern Austria

    NASA Astrophysics Data System (ADS)

    Bruckman, Viktor J.; Hochbichler, Eduard; Yan, Shuai; Glatzel, Gerhard

    2010-05-01

    Recently deciduous forests in northeastern Austria received increased attention as potential sources of biomass for energetic utilisation. There are still substantial deficits in the knowledge on carbon pools, -sequestration and -dynamics at these forest sites. The aim of our study was therefore to identify the main determinants which control soil organic carbon (SOC) pools in differently managed Quercus petraea dominated stands. We used the chronosequence approach to test the influence of stand age and management on the SOC pool. Soil samples were systematically collected from 14 plots by means of a 70mm hand auger to a depth of max. 60cm and separated into five geometric horizons. Narrow O-layers and signs of active bioturbation on most sites suggest rapid carbon mineralisation. Carbon pools of the aboveground biomass, the O horizon as well as fine and coarse roots and decay were determined. Soils in our study are cambisols derived from fossil alluvial deposits and loess and calcic chernozems derived from loess. Total soil carbon was determined by means of dry combustion and subtraction of soil inorganic carbon (SIC, by means of the Scheibler-method) if present. Mean SOC contents ranged from 5.3 kg.m-2 to10.4 kg.m-2 in the entire study area. The highest contents were found in calcic chernozem sites (7.2-10.4 kg.m-2) followed by loamy cambisol (6.1-6.8 kg.m-2) and sandy cambisol sites (5.3-6.9 kg.m-2). Among three chronosequence sets, we found strong positive correlations with total nitrogen (Pearson correlation coefficients of +0.91 to +0.93, p<0.01) and medium strong positive correlations with fine root content (+0.27 to +0.42, p<0.01). In both cases, stronger correlations were observed at cambisol sites. Further medium correlations were found between SOC and decay (+0.23 to +0.42, p<0.01), but no influence of the soil type was observed. As expected, SOC contents decreased significantly with increasing soil depth. Tighter C/N ratios in deeper horizons suggest

  16. Crop residue mass needed to maintain soil organic carbon levels: Can it be determined?

    Technology Transfer Automated Retrieval System (TEKTRAN)

    High yield potential and extensive acreage of corn (Zea mays L.) led to identifying stover as a non-food, herbaceous bioenergy feedstock. A vital aspect of utilizing stover for energy is to establish harvest criteria that avoids exacerbating soil erosion or degrading soil organic carbon (SOC). Our g...

  17. Determination of the organic carbon content in bog and river waters of the taiga zone based on their optical density

    NASA Astrophysics Data System (ADS)

    Efremova, T. T.; Sekretenko, O. P.; Efremov, S. P.

    2014-08-01

    Based on the data of long-term studies of bog and river waters in the taiga zone of Western Siberia, highly significant linear regression models for the relationships between the organic matter content and optical density of the water were developed. The parameters of the relationships obtained are proposed to be used for the determination of the water-soluble carbon content. The inclusion only of the optical density values into the calculated formulas makes them convenient for practical application. Regression models were developed on the basis of the data on determining the carbon content using the bichromate method, which is widely used in soil and hydrochemical studies. The calculated method forms prerequisites for the operational monitoring of the water-soluble organic substances, since the obtained results can be comparable with the earlier published data on the carbon content determined by the same method. These regression models seem to also be suitable for the determination of the organic carbon in the water extracts of organic soils.

  18. COMPARISON OF PROCEDURES TO DETERMINE ADSORPTION CAPACITY OF VOLATILE ORGANIC COMPOUNDS ON ACTIVATED CARBON

    EPA Science Inventory

    Numerous volatile organic compounds (VOCs) are under regulatory consideration for inclusion in the National Primary Drinking Water Standards. Adsorption is a cost-effective treatment technology for control of VOCs. Adsorption capacities were determined for fifteen VOCs in distill...

  19. METHOD 25 - DETERMINATION OF TOTAL GASEOUS NON-METHANE ORGANIC EMISSIONS AS CARBON FROM STATIONARY SOURCES

    EPA Science Inventory

    Section 3.17 describes the procedures and specifications for determining volatile organic compounds as total gaseous non-methane organics from stationary sources. n emission sample is withdrawn from the stack at a constant rate through a heated filter and a chilled condensate tra...

  20. Biophysical Properties as Determinants for Soil Organic Carbon and Total Nitrogen in Grassland Salinization

    PubMed Central

    Pan, Chengchen; Zhao, Halin; Zhao, Xueyong; Han, Huibang; Wang, Yan; Li, Jin

    2013-01-01

    Grassland salinization causes considerable changes to soil and vegetation, which can lead to changes in soil organic carbon (C) and total nitrogen (N). These changes have complex causal relationships. A significant correlation between soil organic C and total N and any soil or vegetation property does not necessarily imply a significant direct effect of the property on soil organic C and total N. In this study, a field survey was conducted to investigate the changes in soil organic C and total N in grassland along a salinity gradient in Hexi corridor, China, and the direct and indirect effects of soil and vegetation properties on both stocks were quantified using a path analysis approach. Significant decrease in soil organic C and total N contents were observed with increasing salinity. Both had significant positive correlations with the Normalized Difference Vegetation Index (NDVI), soil water, and fine particles (silt+clay) content (p<0.01) and significant negative correlations with soil EC, and sand content (p<0.01). NDVI, fine particles content and soil water content had positive direct effects on soil organic C and total N stocks. Soil EC affected soil organic C and total N stocks mainly through its indirect negative effect on NDVI, soil texture, and water content. NDVI, soil texture, and moisture also indirectly affected soil organic C and total N stocks via changes in each other. These indirect effects augmented each other, although in some cases indirect effects worked in opposing directions. PMID:23372776

  1. Method 415.3, Rev. 1.2: Determination of Total Organic Carbon and Specific UV Absorbance at 254 nm in Source Water and Drinking Water

    EPA Science Inventory

    This method provides procedures for the determination of total organic carbon (TOC), dissolved organic carbon (DOC), and UV absorption at 254 nm (UVA) in source waters and drinking waters. The DOC and UVA determinations are used in the calculation of the Specific UV Absorbance (S...

  2. Total organic carbon and gas chromatography-mass spectroscopy methods to determine total carbon and hydrocarbons in mercuric iodide single crystals

    NASA Astrophysics Data System (ADS)

    Steinberg, S.; Kaplan, I.; Schieber, M.; Ortale, C.; Skinner, N.; van den Berg, L.

    1989-11-01

    Total organic carbon was determined by measuring the CO2 produced by combustion in a sealed quartz vessel. The CO2 was quantified by nondispersive IR and by titration using commercial detectors. The total organic carbon was found to be around 10-100 μg/g in both starting materials and in single crystals. Gas chromatography-mass spectroscopy (GC/MS) measurements were made on hexane extracts of mercuric iodide (HgI2) dissolved in potassium iodide solution. Hydrocarbons starting with C10 (DIENE) and up to C26 were found. In addition, phthalates, such as diethyl and dioctyl phthalate were also found. Some of the organic compounds, for example, such hydrocarbons as branched nC16, nC20, nC21, nC22, nC23, and nC24, were present in some HgI2 materials in quantities of the order of weight ppm, but were eliminated in the purification process and were not found in the single crystals. Other organic compounds such as the phthalates were not always eliminated and were identified in the single crystals. In general, the GC/MS could identify only hydrocarbons of C10 and higher which account for only a few percent of the total organic carbon determined by oxidation.

  3. Intercomparison of thermal-optical methods for the determination of organic and elemental carbon: influences of aerosol composition and implications.

    PubMed

    Cheng, Yuan; Duan, Feng-kui; He, Ke-bin; Zheng, Mei; Du, Zhen-yu; Ma, Yong-liang; Tan, Ji-hua

    2011-12-01

    An intercomparison of organic carbon (OC) and elemental carbon (EC) measurements was conducted based on ambient aerosol samples collected during four seasons in Beijing, China. Dependence of OC and EC values on the temperature protocol and the charring correction method is presented and influences of aerosol composition are investigated. EC was found to decrease with the peak inert mode temperature (T(peak)) such that EC determined by the IMPROVE (the Interagency Monitoring of Protected Visual Environments)-A protocol (T(peak) was 580 °C) was 2.85 ± 1.31 and 3.83 ± 2.58 times that measured by an alternative protocol with a T(peak) of 850 °C when using the transmittance and reflectance correction, respectively. It was also found that reflectance correction tends to classify more carbon as EC compared with transmittance; results from the IMPROVE-A protocol showed that the ratio of EC defined by reflectance correction (EC(R)) to that based on transmittance (EC(T)) averaged 1.50 ± 0.42. Moreover, it was demonstrated that emissions from biomass burning would increase the discrepancy between EC values determined by different temperature protocols. On the other hand, the discrepancy between EC(R) and EC(T) was strongly associated with secondary organic aerosol (SOA) which was shown to be an important source of the organics that pyrolyze during the inert mode of thermal-optical analysis. PMID:22044188

  4. Comparison of Remote Sensing Technologies for Determination of Soil Organic Carbon

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soil carbon sequestration is an important component of global carbon balance in the context of ameliorating the effects of carbon dioxide emissions. Remote sensing methods based upon hyperspectral quantification of soil reflectance can provide rapid and cost-effective assessment of soil properties i...

  5. CORRELATIONS FOR THE DETERMINATION OF SURFACE DIFFUSIVITIES OF ORGANIC CHEMICALS ADSORBED ONTO GRANULAR ACTIVATED CARBON

    EPA Science Inventory

    Differential column batch reactor (DCBR) experiments in organic-free water were conducted for the following volatile organic compounds (VOCs): trichloroethene, tetrachloroethene, cis-1,2 dichlorethene, and toluene. Surface diffusion was required to explain the rate of uptake for ...

  6. Automated determination of the stable carbon isotopic composition (δ13C) of total dissolved inorganic carbon (DIC) and total nonpurgeable dissolved organic carbon (DOC) in aqueous samples: RSIL lab codes 1851 and 1852

    USGS Publications Warehouse

    Révész, Kinga M.; Doctor, Daniel H.

    2014-01-01

    The purposes of the Reston Stable Isotope Laboratory (RSIL) lab codes 1851 and 1852 are to determine the total carbon mass and the ratio of the stable isotopes of carbon (δ13C) for total dissolved inorganic carbon (DIC, lab code 1851) and total nonpurgeable dissolved organic carbon (DOC, lab code 1852) in aqueous samples. The analysis procedure is automated according to a method that utilizes a total carbon analyzer as a peripheral sample preparation device for analysis of carbon dioxide (CO2) gas by a continuous-flow isotope ratio mass spectrometer (CF-IRMS). The carbon analyzer produces CO2 and determines the carbon mass in parts per million (ppm) of DIC and DOC in each sample separately, and the CF-IRMS determines the carbon isotope ratio of the produced CO2. This configuration provides a fully automated analysis of total carbon mass and δ13C with no operator intervention, additional sample preparation, or other manual analysis. To determine the DIC, the carbon analyzer transfers a specified sample volume to a heated (70 °C) reaction vessel with a preprogrammed volume of 10% phosphoric acid (H3PO4), which allows the carbonate and bicarbonate species in the sample to dissociate to CO2. The CO2 from the reacted sample is subsequently purged with a flow of helium gas that sweeps the CO2 through an infrared CO2 detector and quantifies the CO2. The CO2 is then carried through a high-temperature (650 °C) scrubber reactor, a series of water traps, and ultimately to the inlet of the mass spectrometer. For the analysis of total dissolved organic carbon, the carbon analyzer performs a second step on the sample in the heated reaction vessel during which a preprogrammed volume of sodium persulfate (Na2S2O8) is added, and the hydroxyl radicals oxidize the organics to CO2. Samples containing 2 ppm to 30,000 ppm of carbon are analyzed. The precision of the carbon isotope analysis is within 0.3 per mill for DIC, and within 0.5 per mill for DOC.

  7. METHODS FOR THE DETERMINATION OF TOTAL ORGANIC CARBON (TOC) IN SOILS AND SEDIMENTS

    EPA Science Inventory

    Organic matter in soils and sediments is widely distributed over the earth's surface occurring in almost all terrestrial and aquatic environments (Schnitzer, 1978). Soils and sediments contain a large variety of organic materials ranging from simple sugars and carbohydrates to th...

  8. Determination of Natural 14C Abundances in Dissolved Organic Carbon in Organic-Rich Marine Sediment Porewaters by Thermal Sulfate Reduction

    NASA Astrophysics Data System (ADS)

    Johnson, L.; Komada, T.

    2010-12-01

    The abundances of natural 14C in dissolved organic carbon (DOC) in the marine environment hold clues regarding the processes that influence the biogeochemical cycling of this large carbon reservoir. At present, UV irradiation is the widely accepted method for oxidizing seawater DOC for determination of their 14C abundances. This technique yields precise and accurate values with low blanks, but it requires a dedicated vacuum line, and hence can be difficult to implement. As an alternative technique that can be conducted on a standard preparatory vacuum line, we modified and tested a thermal sulfate reduction method that was previously developed to determine δ13C values of marine DOC (Fry B. et al., 1996. Analysis of marine DOC using a dry combustion method. Mar. Chem., 54: 191-201.) to determine the 14C abundances of DOC in marine sediment porewaters. In this method, the sample is dried in a 100 ml round-bottom Pyrex flask in the presence of excess oxidant (K2SO4) and acid (H3PO4), and combusted at 550 deg.C. The combustion products are cryogenically processed to collect and quantify CO2 using standard procedures. Materials we have oxidized to date range from 6-24 ml in volume, and 95-1500 μgC in size. The oxidation efficiency of this method was tested by processing known amounts of reagent-grade dextrose and sucrose (as examples of labile organic matter), tannic acid and humic acid (as examples of complex natural organic matter), and porewater DOC extracted from organic-rich nearshore sediments. The carbon yields for all of these materials averaged 99±4% (n=18). The 14C abundances of standard materials IAEA C-6 and IAEA C-5 processed by this method using >1mgC aliquots were within error of certified values. The size and the isotopic value of the blank were determined by a standard dilution technique using IAEA C-6 and IAEA C-5 that ranged in size from 150 to 1500 μgC (n=4 and 2, respectively). This yielded a blank size of 6.7±0.7 μgC, and a blank isotopic

  9. VALIDATION AND IMPROVEMENT OF EPA (ENVIRONMENTAL PROTECTION AGENCY) REFERENCE METHOD 25 - DETERMINATION OF GASEOUS NONMETHANE ORGANIC EMISSIONS AS CARBON

    EPA Science Inventory

    The U.S. Environmental Protection Agency Reference Method 25 measures the total gaseous nonmethane organics as carbon in source emissions. Both laboratory and field studies were conducted to evaluate this method. Tested were the effectiveness of a commercial nonmethane organic an...

  10. [Determination of major, minor and trace elements in soils by polarized energy X-ray fluorescence spectrometry and the application to vertical distribution characteristics of soil organic carbon].

    PubMed

    Shen, Ya-Ting

    2012-11-01

    It is difficult to get accurate, precise and reliable analytical data when using X-ray fluorescence spectrometry (XRF) to determinate sulfur in geological sample. The possible ways to improve sulfur determination accuracy are discussed. Sulfur, and the major, minor and trace elements in soils were determined by polarization energy dispersion XRF (EDXRF) spectrometry and the element profiles and vertical distribution were obtained. Based on this, replacement of two short-term vegetation soil profiles was studied. Significant correlations among the vertical distribution of soil organic carbon content (TOC), organic carbon stable carbon isotopes (delta13C) and several elements were found. The study showed that the EDXRF method can be well applied to element soil geochemical cycle and carbon cycle researches. PMID:23387191

  11. Application and further development of an analytical method for the determination of biogenic total-non methane organic carbon

    NASA Astrophysics Data System (ADS)

    Regnery, Julia; Dindorf, Tamara; Kesselmeier, Juergen

    2010-05-01

    Most of the organic carbon which is present in the atmosphere is found as volatile organic compounds (VOCs). A known dominant source for these volatile organic compounds is the biosphere. Approximately 1.1 Gt of carbon is emitted from biogenic sources every year on a global scale. In comparison only app. 0.15 Gt are emitted from anthropogenic sources. The emission of VOCs has a high influence on the chemical and physical properties of the atmosphere as they contribute to the formation of tropospheric ozone and secondary organic aerosols (SOA). One major limitation in advancing the understanding of this ozone and aerosol generation is the technical ability to accurately measure these volatile organics. Previous studies focused on the detection of a defined set of NMOC (non-methane organic carbon) compounds. However, the integration of these single compound measurements to the sum of organic carbon might only represent a lower limit of atmospheric carbon concentrations, since none of these methods is able to analyze all organic compounds present in the atmosphere as a whole. A few studies are known that report on total NMOC concentration measurements in ambient air but measurements of the total NMOC exchange between vegetation and the atmosphere are missing. The analysis of the total NMOC concentrations is realized by collecting these compounds on a solid adsorbent material. Due to the special characteristics of the utilized adsorbents a separation of the stable gases CO, CO2 and CH4 from the volatile NMOC fraction is achieved. By subsequent heating of the NMOC adsorbent trap the volatiles are desorbed and converted to CO2 in an oxidation unit. The CO2 is collected on a second preconcentration unit followed by thermal desorption and is detected by an infrared gas analyzer. The system was tested with a set of single calibrated VOC species from permeation devices and compared with a data set obtained under field conditions.

  12. Comparison of the quantitative determination of soil organic carbon in coastal wetlands containing reduced forms of Fe and S

    NASA Astrophysics Data System (ADS)

    Passos, Tassia R. G.; Artur, Adriana G.; Nóbrega, Gabriel N.; Otero, Xosé L.; Ferreira, Tiago O.

    2016-06-01

    The performance of the Walkley-Black wet oxidation chemical method for soil organic carbon (SOC) determination in coastal wetland soils (mangroves, coastal lagoons, and hypersaline tidal flats) was evaluated in the state of Ceará along the semiarid coast of Brazil, assessing pyrite oxidation and its effects on soil C stock (SCS) quantification. SOC determined by the chemical oxidation method (CWB) was compared to that assessed by means of a standard elemental analyzer (CEA) for surficial samples (<30 cm depth) from the three wetland settings. The pyrite fraction was quantified in various steps of the chemical oxidation method, evaluating the effects of pyrite oxidation. Regardless of the method used, and consistent with site-specific physicochemical conditions, higher pyrite and SOC contents were recorded in the mangroves, whereas lower values were found in the other settings. CWB values were higher than CEA values. Significant differences in SCS calculations based on CWB and CEA were recorded for the coastal lagoons and hypersaline tidal flats. Nevertheless, the CWB and CEA values were strongly correlated, indicating that the wet oxidation chemical method can be used in such settings. In contrast, the absence of correlation for the mangroves provides evidence of the inadequacy of this method for these soils. Air drying and oxidation decrease the pyrite content, with larger effects rooted in oxidation. Thus, the wet oxidation chemical method is not recommended for mangrove soils, but seems appropriate for SOC/SCS quantification in hypersaline tidal flat and coastal lagoon soils characterized by lower pyrite contents.

  13. Comparison of the quantitative determination of soil organic carbon in coastal wetlands containing reduced forms of Fe and S

    NASA Astrophysics Data System (ADS)

    Passos, Tassia R. G.; Artur, Adriana G.; Nóbrega, Gabriel N.; Otero, Xosé L.; Ferreira, Tiago O.

    2016-02-01

    The performance of the Walkley-Black wet oxidation chemical method for soil organic carbon (SOC) determination in coastal wetland soils (mangroves, coastal lagoons, and hypersaline tidal flats) was evaluated in the state of Ceará along the semiarid coast of Brazil, assessing pyrite oxidation and its effects on soil C stock (SCS) quantification. SOC determined by the chemical oxidation method (CWB) was compared to that assessed by means of a standard elemental analyzer (CEA) for surficial samples (<30 cm depth) from the three wetland settings. The pyrite fraction was quantified in various steps of the chemical oxidation method, evaluating the effects of pyrite oxidation. Regardless of the method used, and consistent with site-specific physicochemical conditions, higher pyrite and SOC contents were recorded in the mangroves, whereas lower values were found in the other settings. CWB values were higher than CEA values. Significant differences in SCS calculations based on CWB and CEA were recorded for the coastal lagoons and hypersaline tidal flats. Nevertheless, the CWB and CEA values were strongly correlated, indicating that the wet oxidation chemical method can be used in such settings. In contrast, the absence of correlation for the mangroves provides evidence of the inadequacy of this method for these soils. Air drying and oxidation decrease the pyrite content, with larger effects rooted in oxidation. Thus, the wet oxidation chemical method is not recommended for mangrove soils, but seems appropriate for SOC/SCS quantification in hypersaline tidal flat and coastal lagoon soils characterized by lower pyrite contents.

  14. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory : determination of nonpurgeable suspended organic carbon by wet-chemical oxidation and infrared spectrometry

    USGS Publications Warehouse

    Burkhardt, Mark R.; Kammer, James A.; Jha, Virendra K.; O'Mara-Lopez, Peggy G.; Woodworth, Mark T.

    1997-01-01

    Precision and accuracy results are described for the determination of nonpurgeable suspended organic carbon (SOC) by silver-filter filtration, wet-chemical oxidation, and infrared determination of hte resulting carbon dioxide (CO2) used at the U.S. Geological Survey's nationalWater Quality Laboratory. An aliquot of raw water isfiltered through a 0.45-micrometer silver filter. The trapped organic material is oxidized using phosphoric acid and potassium persulfate in a scaled glass ampule,and the rseulting CO2 is measured by an infrared CO2 detector. The amount of CO3 is proportional to the concentration of chemically oxidizable nonpurgeable organic carbon in the sample. The SOC method detection limit for routine analysis is 0.2 milligram per liter. The average percent recovery is 97.1 percent and the average standard deviation is 11 percent.

  15. Soil Organic Carbon Input from Urban Turfgrasses

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Turfgrass is a major vegetation type in the urban and suburban environment. Management practices such as species selection, irrigation, and mowing may affect carbon (C) input and storage in these systems. Research was conducted to determine the rate of soil organic carbon (SOC) changes, soil carbon ...

  16. Soil Organic Carbon Input from Urban Turfgrasses

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Turfgrass is a major vegetation type in the urban and suburban environment. Management practices such as species selection, irrigation, and mowing may affect carbon input and storage in these systems. Research was conducted to determine the rate of soil organic carbon (SOC) changes, soil carbon sequ...

  17. Application of high-resolution spectral absorbance measurements to determine dissolved organic carbon concentration in remote areas

    NASA Astrophysics Data System (ADS)

    Avagyan, Armine; Runkle, Benjamin R. K.; Kutzbach, Lars

    2014-09-01

    Accurate quantification of dissolved organic carbon (DOC) in surface and soil pore waters is crucial for understanding changes in water resources under the influence of climate and land use changes. Sampling and laboratory analysis of DOC content at a sufficient temporal frequency are especially difficult to achieve for natural DOC sources like the extensive boreal and arctic mire landscapes due to their remoteness. Therefore, the goals of this paper are (1) to investigate the performance of a portable, high-resolution ultraviolet-visible light spectroscopic method for determining the DOC content of surface and soil pore water samples from a boreal mire complex and (2) to compare the spectroscopic method with other DOC measurement techniques, e.g., the wet heated persulfate oxidation method and a laboratory, expulsion-based spectrophotometric method and (3) to assess different multivariate models that relate absorbance measurements with DOC contents. The study indicates that high-resolution spectroscopic measurements provide a simple, robust and non-destructive method for measuring DOC content. These measurements are of short duration (<1 min) and the sample analysis is portable, rendering this method particularly advantageous for in situ investigations at remote field locations. The study also demonstrates that if absorbances at specific wavelengths are used as proxies for DOC concentration, it is recommended to create site-specific calibration models that include more than one wavelength to achieve the optimal accuracy of the proxy-based DOC quantification.

  18. Determining sources of dissolved organic carbon and disinfection byproduct precursors to the McKenzie River, Oregon

    USGS Publications Warehouse

    Kraus, T.E.C.; Anderson, C.A.; Morgenstern, K.; Downing, B.D.; Pellerin, B.A.; Bergamaschi, B.A.

    2010-01-01

    This study was conducted to determine the main sources of dissolved organic carbon (DOC) and disinfection byproduct (DBP) precursors to the McKenzie River, Oregon (USA). Water samples collected from the mainstem, tributaries, and reservoir outflows were analyzed for DOC concentration and DBP formation potentials (trihalomethanes [THMFPs] and haloacetic acids [HAAFPs]). In addition, optical properties (absorbance and fluorescence) of dissolved organic matter (DOM) were measured to provide insight into DOM composition and assess whether optical properties are useful proxies for DOC and DBP precursor concentrations. Optical properties indicative of composition suggest that DOM in the McKenzie River mainstem was primarily allochthonous - derived from soils and plant material in the upstream watershed. Downstream tributaries had higher DOC concentrations than mainstem sites (1.6 ?? 0.4 vs. 0.7 ?? 0.3 mg L-1) but comprised <5% of mainstem flows and had minimal effect on overall DBP precursor loads. Water exiting two large upstream reservoirs also had higher DOC concentrations than the mainstem site upstream of the reservoirs, but optical data did not support in situ algal production as a source of the added DOC during the study. Results suggest that the first major rain event in the fall contributes DOM with high DBP precursor content. Although there was interference in the absorbance spectra in downstream tributary samples, fluorescence data were strongly correlated to DOC concentration (R 2 = 0.98), THMFP (R2 = 0.98), and HAAFP (R2 = 0.96). These results highlight the value of using optical measurements for identifying the concentration and sources of DBP precursors in watersheds, which will help drinking water utilities improve source water monitoring and management programs. Copyright ?? 2010 by the American Society of Agronomy.

  19. Development of a Total Organic Carbon method for the quantitative determination of solubility enhancement by cyclodextrins: Application to essential oils.

    PubMed

    Kfoury, Miriana; Auezova, Lizette; Greige-Gerges, Hélène; Fourmentin, Sophie

    2016-04-28

    Formation of inclusion complexes with cyclodextrins (CDs) is known to enhance guest solubility in aqueous medium. Different techniques allow determining the evolution in solubility of individual guest compounds. However, examination of mixtures solubility encapsulated in CDs is still a challenge. This is mainly related to the difference in the response of mixture components to the applied technique or to the fact that most of the conventional methods examine the signal of an individual constituent of the mixture. Thus, applying current techniques may not reflect the behavior of the whole mixture. Here, we used for the first time Total Organic Carbon (TOC) analysis to explore and assess the efficiency of 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) to enhance the solubility of natural complex mixtures such as essential oils (EOs). Phase solubility studies were performed for eleven EOs with HP-β-CD. The TOC method has provided good validation parameters for linearity, precision and accuracy. For further validation of the method, phase solubility studies were performed with HP-β-CD for eugenol, as a model EO component. The eugenol solubility was determined by UV-Visible and TOC analyses in order to compare the results. Data obtained from both methods were similar (p < 0.05), thereby proving the effectiveness of the developed TOC method. Finally, the phase solubility diagrams of EOs showed that the solubilizing potential of CD increased proportionally with the decrease in EO intrinsic solubility. Results proved that TOC could be successfully applied to investigate CD/guest inclusion complexes and is expected to have a broad range of applications in the field of mixtures encapsulation. PMID:27046206

  20. Development and application of an analytical method for the determination of total atmospheric biogenic non-methane organic carbon

    NASA Astrophysics Data System (ADS)

    Regnery, J.; Dindorf, T.; Hacker, L.; Andres, S.; Kleist, E.; Wildt, J.; Kesselmeier, J.

    2012-04-01

    Most of the organic carbon which is present in the atmosphere is found as volatile organic compounds (VOCs) dominantly emitted by the biosphere. This biogenic emission has a major impact on the chemical and physical properties of the atmosphere by contributing to the formation of tropospheric ozone and secondary organic aerosol (SOA). One major limitation in advancing the understanding of this ozone and aerosol generation is the technical ability to accurately measure the sum of these volatile organics. Frequently used methods focus on the detection of a defined set of non-methane organic compounds (NMOC). However, adding these single compound concentrations might only represent a lower limit of atmospheric carbon concentrations, since no available method is able to analyze all organic compounds present in the atmosphere. A few studies are known that report on total NMOC concentration measurements in ambient air but measurements of the total NMOC exchange between vegetation and the atmosphere are missing. Therefore, we investigated the analysis of the total NMOC concentration by collecting these compounds on a solid adsorbent material for subsequent total carbon analysis. This first step is necessary to separate the stable gases CO, CO2 and CH4 from the volatile NMOC fraction. NMOC was desorbed and converted to CO2 by passing an oxidation unit. The CO2 is collected on a second preconcentration unit followed by thermal desorption and detection by an infrared gas analyzer. As major difficulties we identified the separation of CO2 from the NMOC compounds on the solid adsorbent unit and the choice of the catalytic material. The measurements were accompanied by GC analysis of single calibrated VOC species from permeation devices and measurements by a PTR-MS. Plant chamber measurements with Quercus ilex showed an expected diurnal course which was confirmed by the NMOC analyzer though with a discrepancy during the day of up to 40 %.

  1. Soil carbon determination by thermogravimetrics

    PubMed Central

    Pallasser, Robert; McBratney, Alex B.

    2013-01-01

    Determination of soil constituents and structure has a vital role in agriculture generally. Methods for the determination of soil carbon have in particular gained greater currency in recent times because of the potential that soils offer in providing offsets for greenhouse gas (CO2-equivalent) emissions. Ideally, soil carbon which can also be quite diverse in its makeup and origin, should be measureable by readily accessible, affordable and reliable means. Loss-on-ignition is still a widely used method being suitably simple and available but may have limitations for soil C monitoring. How can these limitations be better defined and understood where such a method is required to detect relatively small changes during soil-C building? Thermogravimetric (TGA) instrumentation to measure carbonaceous components has become more interesting because of its potential to separate carbon and other components using very precise and variable heating programs. TGA related studies were undertaken to assist our understanding in the quantification of soil carbon when using methods such as loss-on-ignition. Combining instrumentation so that mass changes can be monitored by mass spectrometer ion currents has elucidated otherwise hidden features of thermal methods enabling the interpretation and evaluation of mass-loss patterns. Soil thermogravimetric work has indicated that loss-on-ignition methods are best constrained to temperatures from 200 to 430 °C for reliable determination for soil organic carbon especially where clay content is higher. In the absence of C-specific detection where mass only changes are relied upon, exceeding this temperature incurs increasing contributions from inorganic sources adding to mass losses with diminishing contributions related to organic matter. The smaller amounts of probably more recalcitrant organic matter released at the higher temperatures may represent mineral associated material and/or simply more refractory forms. PMID:23638398

  2. Total organic carbon analyzer

    NASA Technical Reports Server (NTRS)

    Godec, Richard G.; Kosenka, Paul P.; Smith, Brian D.; Hutte, Richard S.; Webb, Johanna V.; Sauer, Richard L.

    1991-01-01

    The development and testing of a breadboard version of a highly sensitive total-organic-carbon (TOC) analyzer are reported. Attention is given to the system components including the CO2 sensor, oxidation reactor, acidification module, and the sample-inlet system. Research is reported for an experimental reagentless oxidation reactor, and good results are reported for linearity, sensitivity, and selectivity in the CO2 sensor. The TOC analyzer is developed with gravity-independent components and is designed for minimal additions of chemical reagents. The reagentless oxidation reactor is based on electrolysis and UV photolysis and is shown to be potentially useful. The stability of the breadboard instrument is shown to be good on a day-to-day basis, and the analyzer is capable of 5 sample analyses per day for a period of about 80 days. The instrument can provide accurate TOC and TIC measurements over a concentration range of 20 ppb to 50 ppm C.

  3. Spatially governed climate factors dominate management in determining the quantity and distribution of soil organic carbon in dryland agricultural systems

    PubMed Central

    Hoyle, Frances C.; O’Leary, Rebecca A.; Murphy, Daniel V.

    2016-01-01

    Few studies describe the primary drivers influencing soil organic carbon (SOC) stocks and the distribution of carbon (C) fractions in agricultural systems from semi-arid regions; yet these soils comprise one fifth of the global land area. Here we identified the primary drivers for changes in total SOC and associated particulate (POC), humus (HOC) and resistant (ROC) organic C fractions for 1347 sample points in the semi-arid agricultural region of Western Australia. Total SOC stock (0–0.3 m) varied from 4 to 209 t C ha−1 with 79% of variation explained by measured variables. The proportion of C in POC, HOC and ROC fractions averaged 28%, 45% and 27% respectively. Climate (43%) and land management practices (32%) had the largest relative influence on variation in total SOC. Carbon accumulation was constrained where average daily temperature was above 17.2 °C and annual rainfall below 450 mm, representing approximately 42% of the 197,300 km2 agricultural region. As such large proportions of this region are not suited to C sequestration strategies. For the remainder of the region a strong influence of management practices on SOC indicate opportunities for C sequestration strategies associated with incorporation of longer pasture phases and adequate fertilisation. PMID:27530805

  4. Spatially governed climate factors dominate management in determining the quantity and distribution of soil organic carbon in dryland agricultural systems.

    PubMed

    Hoyle, Frances C; O'Leary, Rebecca A; Murphy, Daniel V

    2016-01-01

    Few studies describe the primary drivers influencing soil organic carbon (SOC) stocks and the distribution of carbon (C) fractions in agricultural systems from semi-arid regions; yet these soils comprise one fifth of the global land area. Here we identified the primary drivers for changes in total SOC and associated particulate (POC), humus (HOC) and resistant (ROC) organic C fractions for 1347 sample points in the semi-arid agricultural region of Western Australia. Total SOC stock (0-0.3 m) varied from 4 to 209 t C ha(-1) with 79% of variation explained by measured variables. The proportion of C in POC, HOC and ROC fractions averaged 28%, 45% and 27% respectively. Climate (43%) and land management practices (32%) had the largest relative influence on variation in total SOC. Carbon accumulation was constrained where average daily temperature was above 17.2 °C and annual rainfall below 450 mm, representing approximately 42% of the 197,300 km(2) agricultural region. As such large proportions of this region are not suited to C sequestration strategies. For the remainder of the region a strong influence of management practices on SOC indicate opportunities for C sequestration strategies associated with incorporation of longer pasture phases and adequate fertilisation. PMID:27530805

  5. Determination of primary combustion source organic carbon-to-elemental carbon (OC / EC) ratio using ambient OC and EC measurements: secondary OC-EC correlation minimization method

    NASA Astrophysics Data System (ADS)

    Wu, Cheng; Zhen Yu, Jian

    2016-05-01

    Elemental carbon (EC) has been widely used as a tracer to track the portion of co-emitted primary organic carbon (OC) and, by extension, to estimate secondary OC (SOC) from ambient observations of EC and OC. Key to this EC tracer method is to determine an appropriate OC / EC ratio that represents primary combustion emission sources (i.e., (OC / EC)pri) at the observation site. The conventional approaches include regressing OC against EC within a fixed percentile of the lowest (OC / EC) ratio data (usually 5-20 %) or relying on a subset of sampling days with low photochemical activity and dominated by local emissions. The drawback of these approaches is rooted in its empirical nature, i.e., a lack of clear quantitative criteria in the selection of data subsets for the (OC / EC)pri determination. We examine here a method that derives (OC / EC)pri through calculating a hypothetical set of (OC / EC)pri and SOC followed by seeking the minimum of the coefficient of correlation (R2) between SOC and EC. The hypothetical (OC / EC)pri that generates the minimum R2(SOC,EC) then represents the actual (OC / EC)pri ratio if variations of EC and SOC are independent and (OC / EC)pri is relatively constant in the study period. This Minimum R Squared (MRS) method has a clear quantitative criterion for the (OC / EC)pri calculation. This work uses numerically simulated data to evaluate the accuracy of SOC estimation by the MRS method and to compare with two commonly used methods: minimum OC / EC (OC / ECmin) and OC / EC percentile (OC / EC10 %). Log-normally distributed EC and OC concentrations with known proportion of SOC are numerically produced through a pseudorandom number generator. Three scenarios are considered, including a single primary source, two independent primary sources, and two correlated primary sources. The MRS method consistently yields the most accurate SOC estimation. Unbiased SOC estimation by OC / ECmin and OC / EC10 % only occurs when the left tail of

  6. Amount, determining factors and spatial distribution of soil organic carbon storage in the Dano catchment (Southwest Burkina-Faso)

    NASA Astrophysics Data System (ADS)

    Hounkpatin, O.; Op de Hipt, F.; Bossa, A. Y.; Welp, G.; Amelung, W.

    2015-12-01

    The ability to project and to mitigate the impacts of climate change is closely related to the evaluation of soil organic carbon (SOC) content and stock across different types of land use and soil groups. Therefore, this study aimed at estimating the surface and subsoil organic carbon stocks in different land use systems and across various soil groups. A further aim was to assess the spatial variability of SOC content and stocks and how this is controlled by climate and site properties. The Random Forest (RF) modelling was used and compared to Ordinary Kriging interpolation (OK) for the topsoil SOC and stock. About 70 soil profiles were described along 16 transects with 197 samples collected from different horizons up to 1 m depth where possible. In addition, 1205 samples were collected within an intensive auger grid mapping. Mid-infrared spectroscopy and partial least-squares analysis were used as a fast and low-cost technique to handle the large amount of samples for the SOC estimation. The natural/semi natural vegetation recorded the highest SOC stock in the topsoil (28.6 t C ha-1) as compared to the cropland (25.5 t C ha-1). Over 1 m depth, Gleysols (87.4 t C ha-1) stored the highest amount of SOC stock followed by the Cambisols (76. t C ha-1) and the Plinthosols (73.1 t C ha-1) while the lowest were found in the Lixisols (57.8 t C ha-1). For the topsoil, the RF model revealed soil properties such as cation exchange capacity (CEC) and stone content as main factors affecting SOC content variability while CEC and bulk density were the major drivers for the subsoil. The carbon stock variability was mainly affected by the CEC and the reference soil group in the topsoil while horizon thickness and bulk density constituted the main factors for the subsoil. The geostatistical evaluation proved that the SOC content in the Dano catchment has a moderate spatial autocorrelation while the carbon stock was strongly spatially dependent. The RF gave a better prediction for

  7. Bioanalytical effect-balance model to determine the bioavailability of organic contaminants in sediments affected by black and natural carbon.

    PubMed

    Bräunig, Jennifer; Tang, Janet Y M; Warne, Michael St J; Escher, Beate I

    2016-08-01

    In sediments several binding phases dictate the fate and bioavailability of organic contaminants. Black carbon (BC) has a high sorptive capacity for organic contaminants and can limit their bioavailability, while the fraction bound to organic carbon (OC) is considered to be readily desorbable and bioavailable. We investigated the bioavailability and mixture toxicity of sediment-associated contaminants by combining different extraction techniques with in vitro bioanalytical tools. Sediments from a harbour with high fraction of BC, and sediments from remote, agricultural and urban areas with lower BC were treated with exhaustive solvent extraction, Tenax extraction and passive sampling to estimate total, bioaccessible and bioavailable fractions, respectively. The extracts were characterized with cell-based bioassays that measure dioxin-like activity (AhR-CAFLUX) and the adaptive stress response to oxidative stress (AREc32). Resulting bioanalytical equivalents, which are effect-scaled concentrations, were applied in an effect-balance model, consistent with a mass balance-partitioning model for single chemicals. Sediments containing BC had most of the bioactivity associated to the BC fraction, while the OC fraction played a role for sediments with lower BC. As effect-based sediment-water distribution ratios demonstrated, most of the bioactivity in the AhR-CAFLUX was attributable to hydrophobic chemicals while more hydrophilic chemicals activated AREc32, even though bioanalytical equivalents in the aqueous phase remained negligible. This approach can be used to understand the fate and effects of mixtures of diverse organic contaminants in sediments that would not be possible if single chemicals were targeted by chemical analysis; and make informed risk-based decisions concerning the management of contaminated sediments. PMID:27176940

  8. Approaches to Determining the Oxidation State of Nitrogen and Carbon Atoms in Organic Compounds for High School Students

    ERIC Educational Resources Information Center

    Jurowski, Kamil; Krzeczkowska, Malgorzata Krystyna; Jurowska, Anna

    2015-01-01

    The concept of oxidation state (or oxidation number) and related issues have always been difficult for students. In addition, there are misunderstandings and obscurities, which can cause improper balancing of the chemical equations (mostly in organic reactions). In particular, these problems are related to determination of the oxidation state of…

  9. Simultaneous determination of mercury and organic carbon in sediment and soils using a direct mercury analyzer based on thermal decomposition-atomic absorption spectrophotometry.

    PubMed

    Chen, Jingjing; Chakravarty, Pragya; Davidson, Gregg R; Wren, Daniel G; Locke, Martin A; Zhou, Ying; Brown, Garry; Cizdziel, James V

    2015-04-29

    The purpose of this work was to study the feasibility of using a direct mercury analyzer (DMA) to simultaneously determine mercury (Hg) and organic matter content in sediment and soils. Organic carbon was estimated by re-weighing the sample boats post analysis to obtain loss-on-ignition (LOI) data. The DMA-LOI results were statistically similar (p<0.05) to the conventional muffle furnace approach. A regression equation was developed to convert DMA-LOI data to total organic carbon (TOC), which varied between 0.2% and 13.0%. Thus, mercury analyzers based on combustion can provide accurate estimates of organic carbon content in non-calcareous sediment and soils; however, weight gain from moisture (post-analysis), measurement uncertainty, and sample representativeness should all be taken into account. Sediment cores from seasonal wetland and open water areas from six oxbow lakes in the Mississippi River alluvial flood plain were analyzed. Wetland sediments generally had higher levels of Hg than open water areas owing to a greater fraction of fine particles and higher levels of organic matter. Annual loading of Hg in open water areas was estimated at 4.3, 13.4, 19.2, 20.7, 129, and 135 ng cm(-2) yr(-1) for Beasley, Roundaway, Hampton, Washington, Wolf and Sky Lakes, respectively. Generally, the interval with the highest Hg flux was dated to the 1960s and 1970s. PMID:25847156

  10. Mobility of organic carbon from incineration residues

    SciTech Connect

    Ecke, Holger Svensson, Malin

    2008-07-01

    Dissolved organic carbon (DOC) may affect the transport of pollutants from incineration residues when landfilled or used in geotechnical construction. The leaching of dissolved organic carbon (DOC) from municipal solid waste incineration (MSWI) bottom ash and air pollution control residue (APC) from the incineration of waste wood was investigated. Factors affecting the mobility of DOC were studied in a reduced 2{sup 6-1} experimental design. Controlled factors were treatment with ultrasonic radiation, full carbonation (addition of CO{sub 2} until the pH was stable for 2.5 h), liquid-to-solid (L/S) ratio, pH, leaching temperature and time. Full carbonation, pH and the L/S ratio were the main factors controlling the mobility of DOC in the bottom ash. Approximately 60 weight-% of the total organic carbon (TOC) in the bottom ash was available for leaching in aqueous solutions. The L/S ratio and pH mainly controlled the mobilization of DOC from the APC residue. About 93 weight-% of TOC in the APC residue was, however, not mobilized at all, which might be due to a high content of elemental carbon. Using the European standard EN 13 137 for determination of total organic carbon (TOC) in MSWI residues is inappropriate. The results might be biased due to elemental carbon. It is recommended to develop a TOC method distinguishing between organic and elemental carbon.

  11. Method for determining stable isotope ratios of dissolved organic carbon in interstitial and other natural marine waters

    NASA Technical Reports Server (NTRS)

    Bauer, J. E.; Haddad, R. I.; Des Marais, D. J.

    1991-01-01

    A procedure is described for the analysis of the stable carbon isotopic composition of dissolved organic carbon (DOC) in natural waters from marine and higher-salinity environments. Rapid (less than 5 min) and complete oxidation of DOC is achieved using a modification of previous photochemical oxidation techniques. The CO2 evolved from DOC oxidation can be collected in less than 10 min for isotopic analysis. The procedure is at present suitable for oxidation and collection of 1-5 micromoles of carbon and has an associated blank of 0.1-0.2 micromole of carbon. Complete photochemical oxidation of DOC standards was demonstrated by quantitative recovery of CO2 as measured manometrically. Isotopic analyses of standards by photochemical and high-temperature sealed-tube combustion methods agreed to within 0.3%. Photochemical oxidation of DOC in a representative sediment pore-water sample was also quantitative, as shown by the excellent agreement between the photochemical and sealed-tube methods. The delta 13C values obtained for pore-water DOC using the two methods of oxidation were identical, suggesting that the modified photochemical method is adequate for the isotopically non-fractionated oxidation of pore-water DOC. The procedure was evaluated through an analysis of DOC in pond and pore waters from a hypersaline microbial mat environment. Concentrations of DOC in the water column over the mat displayed a diel pattern, but the isotopic composition of this DOC remained relatively constant (average delta 13C = -12.4%). Pore-water DOC exhibited a distinct concentration maximum in the mat surface layer, and delta 13C of pore-water DOC was nearly 8% lighter at 1.5-2.0-cm depth than in the mat surface layer (0-0.5-cm depth). These results demonstrate the effectiveness of the method in elucidating differences in DOC concentration and delta 13C over biogeochemically relevant spatial and temporal scales. Carbon isotopic analysis of DOC in natural waters, especially pore waters

  12. Comparison of two thermal-optical methods for the determination of organic carbon and elemental carbon: Results from the southeastern United States

    NASA Astrophysics Data System (ADS)

    Cheng, Yuan; Zheng, Mei; He, Ke-bin; Chen, Yingjun; Yan, Bo; Russell, Armistead G.; Shi, Wenyan; Jiao, Zheng; Sheng, Guoying; Fu, Jiamo; Edgerton, Eric S.

    2011-02-01

    A total of 333 PM 2.5 samples were collected at four sites in the southeastern Aerosol Research and Characterization Study (SEARCH) network during four seasons from 2003 to 2005 and were simultaneously analyzed by two common thermal-optical methods, the National Institute of Occupational Safety and Health (NIOSH) method and the Interagency Monitoring of Protected Visual Environments (IMPROVE) method. The concentrations of total carbon measured by the two methods were comparable, whereas the split of organic carbon (OC) and elemental carbon (EC) was significantly different. The NIOSH-defined EC was lower (up to 80%) than that defined by IMPROVE since the NIOSH method applied the transmittance charring correction and a much higher peak inert mode temperature. The discrepancy between NIOSH- and IMPROVE-defined EC showed distinct seasonal and spatial variations. Potential factors contributing to this discrepancy besides the analytical method were investigated. The discrepancy between NIOSH- and IMPROVE-defined EC was larger in the spring compared to winter due to the influence of biomass burning, which is known to emit significant amount of brown carbon that would complicate the split of OC and EC. The NIOSH-defined EC to IMPROVE-defined EC ratio reached its minimum (0.2-0.5) in the summer, when the largest discrepancy was observed. This was most likely to be attributed to the influence of secondary organic aerosol (SOA). Moreover, the discrepancy between NIOSH- and IMPROVE-defined EC was larger in the coastal and the rural sites where the presence of abundant SOA was found based on previous studies in this region, providing supporting evidence that SOA could contribute to the observed discrepancy in summer.

  13. Dispersion and separation of nanostructured carbon in organic solvents

    NASA Technical Reports Server (NTRS)

    Landi, Brian J. (Inventor); Raffaelle, Ryne P. (Inventor); Ruf, Herbert J. (Inventor); Evans, Christopher M. (Inventor)

    2011-01-01

    The present invention relates to dispersions of nanostructured carbon in organic solvents containing alkyl amide compounds and/or diamide compounds. The invention also relates to methods of dispersing nanostructured carbon in organic solvents and methods of mobilizing nanostructured carbon. Also disclosed are methods of determining the purity of nanostructured carbon.

  14. Method of Analysis by the U.S. Geological Survey California District Sacramento Laboratory-- Determination of Dissolved Organic Carbon in Water by High Temperature Catalytic Oxidation, Method Validation, and Quality-Control Practices

    USGS Publications Warehouse

    Bird, Susan M.; Fram, Miranda S.; Crepeau, Kathryn L.

    2003-01-01

    An analytical method has been developed for the determination of dissolved organic carbon concentration in water samples. This method includes the results of the tests used to validate the method and the quality-control practices used for dissolved organic carbon analysis. Prior to analysis, water samples are filtered to remove suspended particulate matter. A Shimadzu TOC-5000A Total Organic Carbon Analyzer in the nonpurgeable organic carbon mode is used to analyze the samples by high temperature catalytic oxidation. The analysis usually is completed within 48 hours of sample collection. The laboratory reporting level is 0.22 milligrams per liter.

  15. Determination of octanol-water partition coefficients for carbonate esters and other small organic molecules by microemulsion electrokinetic chromatography.

    PubMed

    Østergaard, Jesper; Hansen, Steen Honoré; Larsen, Claus; Schou, Christian; Heegaard, Niels H H

    2003-03-01

    Microemulsion electrokinetic chromatography (MEEKC) was assessed as a tool for determination of octanol-water partition coefficients using 34 solutes encompassing 8 carbonate esters. It was confirmed that microemulsions containing 1.44-2.88% w/w SDS, 6.49% w/w 1-butanol, and 0.82% w/w n-heptane constitute a good model of octanol-water partitioning in the pH range of 1.4-7.4. Use of the migration index concept led to improved repeatability of the MEEKC method compared to the use of retention factors. Using a dynamical coating, a high electroosmotic flow at pH 1.4 and 4.75 was achieved expanding the practical pH working range of the MEEKC system. The correlation obtained between the migration index and log P was unaffected by pH indicating that the properties of the microemulsion droplets and, thus, partitioning are independent of pH. No evidence for congeneric behavior was found for the sample set comprising solutes with different hydrogen bonding properties suggesting that simple reference compounds can be used as calibrators. Lipophilicity estimates for the series of carbonate esters were obtained. The increase in lipophilicity with chain length was smaller than expected from the Hansch substituent constant, pi. PMID:12658693

  16. Development of a combined isotopic and mass-balance approach to determine dissolved organic carbon sources in eutrophic reservoirs.

    PubMed

    Pierson-Wickmann, Anne-Catherine; Gruau, Gérard; Jardé, Emilie; Gaury, Nicolas; Brient, Luc; Lengronne, Marion; Crocq, André; Helle, Daniel; Lambert, Thibault

    2011-04-01

    A combined mass-balance and stable isotope approach was set up to identify and quantify dissolved organic carbon (DOC) sources in a DOC-rich (9mgL(-1)) eutrophic reservoir located in Western France and used for drinking water supply (so-called Rophemel reservoir). The mass-balance approach consisted in measuring the flux of allochthonous DOC on a daily basis, and in comparing it with the effective (measured) DOC concentration of the reservoir. The isotopic approach consisted, for its part, in measuring the carbon isotope ratios (δ(13)C values) of both allochthonous and autochthonous DOC sources, and comparing these values with the δ(13)C values of the reservoir DOC. Results from both approaches were consistent pointing out for a DOC of 100% allochthonous origin. In particular, the δ(13)C values of the DOC recovered in the reservoir (-28.5±0.2‰; n=22) during the algal bloom season (May-September) showed no trace of an autochthonous contribution (δ(13)C in algae=-30.1±0.3‰; n=2) being indistinguishable from the δ(13)C values of allochthonous DOC from inflowing rivers (-28.6±0.1‰; n=8). These results demonstrate that eutrophication is not responsible for the high DOC concentrations observed in the Rophemel reservoir and that limiting eutrophication of this reservoir will not reduce the potential formation of disinfection by-products during water treatment. The methodology developed in this study based on a complementary isotopic and mass-balance approach provides a powerful tool, suitable to identify and quantify DOC sources in eutrophic, DOC-contaminated reservoirs. PMID:21190712

  17. Soil organic carbon across scales.

    PubMed

    O'Rourke, Sharon M; Angers, Denis A; Holden, Nicholas M; McBratney, Alex B

    2015-10-01

    Mechanistic understanding of scale effects is important for interpreting the processes that control the global carbon cycle. Greater attention should be given to scale in soil organic carbon (SOC) science so that we can devise better policy to protect/enhance existing SOC stocks and ensure sustainable use of soils. Global issues such as climate change require consideration of SOC stock changes at the global and biosphere scale, but human interaction occurs at the landscape scale, with consequences at the pedon, aggregate and particle scales. This review evaluates our understanding of SOC across all these scales in the context of the processes involved in SOC cycling at each scale and with emphasis on stabilizing SOC. Current synergy between science and policy is explored at each scale to determine how well each is represented in the management of SOC. An outline of how SOC might be integrated into a framework of soil security is examined. We conclude that SOC processes at the biosphere to biome scales are not well understood. Instead, SOC has come to be viewed as a large-scale pool subjects to carbon flux. Better understanding exists for SOC processes operating at the scales of the pedon, aggregate and particle. At the landscape scale, the influence of large- and small-scale processes has the greatest interaction and is exposed to the greatest modification through agricultural management. Policy implemented at regional or national scale tends to focus at the landscape scale without due consideration of the larger scale factors controlling SOC or the impacts of policy for SOC at the smaller SOC scales. What is required is a framework that can be integrated across a continuum of scales to optimize SOC management. PMID:25918852

  18. Solid-phase extraction using bis(indolyl)methane-modified silica reinforced with multiwalled carbon nanotubes for the simultaneous determination of flavonoids and aromatic organic acid preservatives.

    PubMed

    Wang, Na; Liao, Yuan; Wang, Jiamin; Tang, Sheng; Shao, Shijun

    2015-12-01

    A novel bis(indolyl)methane-modified silica reinforced with multiwalled carbon nanotubes sorbent for solid-phase extraction was designed and synthesized by chemical immobilization of nitro-substituted 3,3'-bis(indolyl)methane on silica modified with multiwalled carbon nanotubes. Coupled with high-performance liquid chromatography analysis, the extraction properties of the sorbent were evaluated for flavonoids and aromatic organic acid compounds. Under optimum conditions, the sorbent can simultaneously extract five flavonoids and two aromatic organic acid preservatives in aqueous solutions in a single-step solid-phase extraction procedure. Wide linear ranges were obtained with correlation coefficients (R(2) ) ranging from 0.9843 to 0.9976, and the limits of detection were in the range of 0.5-5 μg/L for the compounds tested. Compared with the silica modified with multiwalled carbon nanotubes sorbent and the nitro-substituted 3,3'-bis(indolyl)methane-modified silica sorbent, the developed sorbent exhibited higher extraction efficiency toward the selected analytes. The synergistic effect of nitro-substituted 3,3'-bis(indolyl)methane and multiwalled carbon nanotubes not only improved the surface-to-volume ratio but also enhanced multiple intermolecular interactions, such as hydrogen bonds, π-π, and hydrophobic interactions, between the new sorbent and the selected analytes. The as-established solid-phase extraction with high-performance liquid chromatography and diode array detection method was successfully applied to the simultaneous determination of flavonoids and aromatic organic acid preservatives in grape juices with recoveries ranging from 83.9 to 112% for all the selected analytes. PMID:26529362

  19. Analytical strategy for the determination of various arsenic species in landfill leachate containing high concentrations of chlorine and organic carbon by HPLC-ICPMS

    NASA Astrophysics Data System (ADS)

    Bae, J.; An, J.; Kim, J.; Jung, H.; Kim, K.; Yoon, C.; Yoon, H.

    2012-12-01

    As a variety of wastes containing arsenic are disposed of in landfills, such facilities can play a prominent role in disseminating arsenic sources to the environment. Since it is widely recognized that arsenic toxicity is highly dependent on its species, accurate determination of various arsenic species should be considered as one of the essential goals to properly account for the potential health risk of arsenic in human and the environment. The inductively coupled plasma mass spectrometry linked to high performance liquid chromatography (HPLC-ICPMS) is acknowledged as one of the most important tools for the trace analysis of metallic speciation because of its superior separation capability and detectability. However, the complexity of matrices can cause severe interferences in the analysis results, which is the problem often encountered with HPLC-ICPMS system. High concentration of organic carbon in a sample solution causes carbon build-up on the skimmer and sampling cone, which reduces analytical sensitivity and requires a high maintenance level for its cleaning. In addition, argon from the plasma and chlorine from the sample matrix may combine to form 40Ar35Cl, which has the same nominal mass to charge (m/z) ratio as arsenic. In this respect, analytical strategy for the determination of various arsenic species (e.g., inorganic arsenite and arsenate, monomethylarsonic acid, dimethylarsinic acid, dimethyldithioarsinic acid, and arsenobetaine) in landfill leachate containing high concentrations of chlorine and organic carbon was developed in the present study. Solid phase extraction disk (i.e., C18 disk), which does not significantly adsorb any target arsenic species, was used to remove organic carbon in sample solutions. In addition, helium (He) gas was injected into the collision reaction cell equipped in ICPMS to collapse 40Ar35Cl into individual 40Ar and 35Cl. Although He gas also decreased arsenic intensity by blocking 75As, its signal to noise ratio

  20. Automated method for determination of dissolved organic carbon-water distribution constants of structurally diverse pollutants using pre-equilibrium solid-phase microextraction.

    PubMed

    Ripszam, Matyas; Haglund, Peter

    2015-02-01

    Dissolved organic carbon (DOC) plays a key role in determining the environmental fate of semivolatile organic environmental contaminants. The goal of the present study was to develop a method using commercially available hardware to rapidly characterize the sorption properties of DOC in water samples. The resulting method uses negligible-depletion direct immersion solid-phase microextraction (SPME) and gas chromatography-mass spectrometry. Its performance was evaluated using Nordic reference fulvic acid and 40 priority environmental contaminants that cover a wide range of physicochemical properties. Two SPME fibers had to be used to cope with the span of properties, 1 coated with polydimethylsiloxane and 1 coated with polystyrene divinylbenzene polydimethylsiloxane, for nonpolar and semipolar contaminants, respectively. The measured DOC-water distribution constants showed reasonably good reproducibility (standard deviation ≤ 0.32) and good correlation (R(2)  = 0.80) with log octanol-water partition coefficients for nonpolar persistent organic pollutants. The sample pretreatment is limited to filtration, and the method is easy to adjust to different DOC concentrations. These experiments also utilized the latest SPME automation that largely decreases total cycle time (to 20 min or shorter) and increases sample throughput, which is advantageous in cases when many samples of DOC must be characterized or when the determinations must be performed quickly, for example, to avoid precipitation, aggregation, and other changes of DOC structure and properties. The data generated by this method are valuable as a basis for transport and fate modeling studies. PMID:25393710

  1. Improved method for the determination of nonpurgeable suspended organic carbon in natural water by silver filter filtration, wet chemical oxidation, and infrared spectrometry

    USGS Publications Warehouse

    Burkhardt, M.R.; Brenton, R.W.; Kammer, J.A.; Jha, V.K.; O'Mara-Lopez, P. G.; Woodworth, M.T.

    1999-01-01

    Precision and accuracy are reported for the first time for the analysis of nonpurgeable suspended organic carbon by silver membrane filtration followed by wet chemical oxidation. A water sample is pressure filtered through a 0.45-??m-pore-size, 47-mm-diameter silver membrane filter. The silver membrane filter then is cut into ribbons and placed in a flame-sealable glass ampule. The organic material trapped on the membrane filter strips is acidified, purged with oxygen to remove inorganic carbonates and volatile organic compounds, and oxidized to carbon dioxide (CO2) using phosphoric acid and potassium persulfate in the sealed glass ampule. The resulting CO2 is measured by a nondispersive infrared CO2 detector. The amount of CO2 is proportional to the concentration of chemically oxidizable nonpurgeable organic carbon in the environmental water sample. The quantitation and method detection limit for routine analysis is 0.2 mg/L. The average percent recovery in five representative matrices was 97 ?? 11%. The errors associated with sampling and sample preparation of nonpurgeable suspended organic carbon are also described.Precision and accuracy are reported for the first time for the analysis of nonpurgeable suspended organic carbon by silver membrane filtration followed by wet chemical oxidation. A water sample is pressure filtered through a 0.45-??m-pore-size, 47-mm-diameter silver membrane filter. The silver membrane filter then is cut into ribbons and placed in a flame-sealable glass ampule. The organic material trapped on the membrane filter strips is acidified, purged with oxygen to remove inorganic carbonates and volatile organic compounds, and oxidized to carbon dioxide (CO2) using phosphoric acid and potassium persulfate in the sealed glass ampule. The resulting CO2 is measured by a nondispersive infrared CO2 detector. The amount of CO2 is proportional to the concentration of chemically oxidizable nonpurgeable organic carbon in the environmental water sample

  2. The Quest for Organic Carbon on Mars

    NASA Technical Reports Server (NTRS)

    Eigenbrode, Jennifer

    2011-01-01

    We are entering an era of Mars exploration in which organic carbon detection, characterization, and structural identification will be key to addressing some of the outstanding science objectives of the Mars Exploration Program. Success of these missions will depend on technical, scientific, and strategic elements--all of which are strongly determined based on terrestrial experience and knowledge of organic matter formation, concentration, and preservation. Analog studies including Precambrian sediments, modern endolithic communities, and experiments help us fine-tune these approaches, but we also need to expect the unexpected. This presentation will provide perspective on the challenges of detecting organic carbon on Mars, how we may achieve such detections with the in situ instruments, such as the SAM (Science Analysis at Mars) instrument suite onboard Curiosity, the rover for the 2011 Mars Science Laboratory mission.

  3. Effects of thermal maturation on stable organic carbon isotopes as determined by hydrous pyrolysis of Woodford Shale

    NASA Astrophysics Data System (ADS)

    Lewan, M. D.

    1983-08-01

    Acquiring crude oils that have been expelled from the same rock unit at different levels of thermal maturation is currently not feasible in the natural system. This prevents direct correlation of compositional changes between the organic matter retained in a source rock and its expelled crude oil at different levels of thermal maturation. Alleviation of this deficiency in studying the natural system requires the use of laboratory experiments. Natural generation of petroleum from amorphous type-II kerogen in the Woodford Shale may be simulated by hydrous pyrolysis, which involves heating crushed rock in contact with water at subcritical temperatures (<374°C). Four distinct stages of petroleum generation are observed from this type of pyrolysis; (1) pre-oil generation, (2) incipient-oil generation, (3) primary-oil generation, and (4) post-oil generation. The effects of thermal maturation on the δ 13C values of kerogen, bitumen, and expelled oil-like pyrolysate from the Woodford Shale have been studied through these four stages of petroleum generation. Similar to the natural system, the kerogens isolated from the pyrolyzed rock showed no significant change in δ 13C. This suggests that the δ 13C value of kerogens may be useful in kerogen typing and oil-to-source rock correlations. δ 13C values of bitumens extracted from the pyrolyzed rock showed an initial decrease during the incipient-oil generation stage, followed by depletion during the primary- and post-oil generation stages. This reversal is not favorable for geochemical correlation or maturity evaluation. Saturated and polar components of the bitumen show the greatest δ 13C variations with increasing thermal maturation. The difference between the δ 13C of these two components gives a unidirectional trend that serves as a general indicator of thermal maturation and is referred to as the bitumen isotope index (BII). δ 13C values of the expelled pyrolysates show a unidirectional increase with increasing

  4. Carbon sources and cycle in the western Mediterranean—the use of molecular markers to determine the origin of organic matter

    NASA Astrophysics Data System (ADS)

    Bouloubassi, I.; Lipiatou, E.; Saliot, A.; Tolosa, I.; Bayona, J. M.; Albaigés, J.

    A series of molecular organic markers were determined in surface sediment samples collected in the Rhone and Ebro prodeltas and the western Mediterranean Basin in order to map and estimate the flux of naturally-derived organic matter inputs to the area. Continental and marine inputs were characterized by the distributions of n-alkanes, n-fatty acids, sterols, and polycyclic aromatic hydrocarbons (PAHs) such as retene, perylene and tetrahydrochrysenes (ΣTHC). The distribution of terrestrial markers evidenced the influence of rivers as main vectors of continentally-derived inputs in the area. In the data set of the Rhone delta and slope, including stations from the Gulf of Lions, significant correlations were observed between the organic content of sediment and the ΣTHC and retene concentrations (R2 = 0.88 and 0.68, respectively) and between ETHC levels and the δ13C of the organic matter (R2 = 0.89). The transport and settling of naturally-derived terrigenous material in the Ebro prodelta were reflected by the distribution of vascular plant n-alkanes. These refractory materials were preserved in the deep basin. Additionally, the distributions of fatty acids and sterols in the Ebro prodelta clearly evidenced algal signatures resulting from the enrichment of deltaic waters by nutrients transported by the river. Based on biomarker data a criterion is proposed to assess the percentage of terrestrial organic carbon in sediments, considering the river mouth sediment as the continental end-member. Fluxes of terrigenous organic inputs were calculated using sediment accumulation rates. Depositional flux estimates for the deltaic area off the Rhone River (∼ 15 340 km2) were as follows: 216 kg/year for ΣTHC, 104 kg/year for retene, 11 t/year for terrestrial n-alkanes. The accumulation rates in the area of influence of the Ebro River (∼ 12 600 km2) were 69 kg/year for retene and 6 t/year for terrestrial n-alkanes. Comparison of these data with estimates of riverine

  5. Seasonal variation in soil organic carbon

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Organic carbon in soil is most often measured at a single point in time, under the assumption that the major pools of organic carbon change so slowly that variation over weeks or months will be insignificant. The validity of this assumption has implications for accurate comparison of soil carbon bet...

  6. Worldwide organic soil carbon and nitrogen data

    SciTech Connect

    Zinke, P.J.; Stangenberger, A.G.; Post, W.M.; Emanuel, W.R.; Olson, J.S.

    1984-05-01

    A compilation of soil carbon and nitrogen storage data for more than 3500 soil profiles from under natural vegetation or relatively undisturbed sites is presented in this report. A summary table of the carbon and nitrogen storage in a pedon of surface cubic meter for each soil profile, as well as location, elevation, climate, parent material, and vegetation information, are presented. The data were used to determine average carbon and nitrogen storage on land surfaces of the world. Calculations were also made of storage related to climatic classifications, ecosystem clasifications, and latitudinal increments from the equator to 75/sup 0/. Carbon (kg.m/sup -3/) varies from 2 in hot dry climates, through 10 in many cold dry or seasonally moist (warm or hot) climates, to more than 30 in wet alpine or subpolar climates. Nitrogen storage, an order of magnitude smaller than carbon storage in soils, shows broad parallels but exceeds 1600 g.m/sup -3/ for subtropical/tropical premontane or lower montane soils, as well as alpine or subpolar wet soils. Such limiting conditions, defined by a balance of income and loss rates for mature soil profiles, also explain much of the variation among major ecosystem complexes whose soils are partly disturbed, incompletely recovered, or imperfectly known regarding their maturity and stability. Classifying profiles into Holdridge life zones and using appropriate life zone areas, we estimate 1309 x 10/sup 15/ g carbon and 92 x 10/sup 15/ g nitrogen in the world's soils. Alternatively, using average organic carbon and nitrogen densities from one degree latitude bands multiplied by the earth's surface area in the respective bands, we arrive at 1728 x 10/sup 15/ g of carbon and 117 x 10/sup 15/ g of nitrogen. Inadequacies that lead to the disparate estimates are discussed. 123 references, 5 figures, 7 tables.

  7. Determination of adsorbable organic fluorine from aqueous environmental samples by adsorption to polystyrene-divinylbenzene based activated carbon and combustion ion chromatography.

    PubMed

    Wagner, Andrea; Raue, Brigitte; Brauch, Heinz-Jürgen; Worch, Eckhard; Lange, Frank T

    2013-06-21

    A new method for the determination of trace levels of adsorbable organic fluorine (AOF) in water is presented. Even if the individual contributing target compounds are widely unknown, this surrogate parameter is suited to identify typical organofluorine contaminations, such as with polyfluorinated chemicals (PFCs), and represents a lower boundary of the organofluorine concentration in water bodies. It consists of the adsorption of organofluorine chemicals on a commercially available synthetic polystyrene-divinylbenzene based activated carbon (AC) followed by analysis of the loaded AC by hydropyrolysis combustion ion chromatography (CIC). Inorganic fluorine is displaced by excess nitrate during the extraction step and by washing the loaded activated carbon with an acidic sodium nitrate solution. Due to its high purity the synthetic AC had a very low and reproducible fluorine blank (0.3 μg/g) compared to natural ACs (up to approximately 9 μg/g). Using this AC, fluoride and the internal standard phosphate could be detected free of chromatographic interferences. With a sample volume of 100 mL and 2× 100 mg of AC packed into two extraction columns combined in series, a limit of quantification (LOQ), derived according to the German standard method DIN 32645, of 0.3 μg/L was achieved. The recoveries of six model PFCs were determined from tap water and a municipal wastewater treatment plant (WWTP) effluent. Except for the extremely polar perfluoroacetic acid (recovery of approximately 10%) the model substances showed fairly good (50% for perfluorobutanoic acid (PFBA)) to very good fluorine recoveries (100±20% for perfluorooctanoic acid (PFOA), perfluorobutanesulfonate (PFBS), 6:2 fluorotelomersulfonate (6:2 FTS)), both from tap water and wastewater matrix. This new analytical protocol was exemplarily applied to several surface water and groundwater samples. The obtained AOF values were compared to the fluorine content of 19 target PFCs analyzed by high performance

  8. Variability of organic and elemental carbon, water soluble organic carbon, and isotopes in Hong Kong

    NASA Astrophysics Data System (ADS)

    Ho, K. F.; Lee, S. C.; Cao, J. J.; Li, Y. S.; Chow, J. C.; Watson, J. G.; Fung, K.

    2006-10-01

    To determine the levels and variations of carbonaceous aerosol in Hong Kong, PM2.5 and PM10 samples were collected by high volume (Hi-vol) samplers at three monitoring stations (representing middle-scale roadside, urban-, and regional-scale environments) during winter (November 2000 to February 2001) and summer (June 2001 to August 2001) periods. The highest concentrations of organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) were found at the middle-scale roadside site with the lowest at the regional-scale site. The percentages of WSOC in total carbon at these sites were inversely correlated with their concentrations (i.e., the highest percentages of WSOC were observed at the regional-scale site). A high WSOC fraction may be associated with aged aerosol because of the secondary formation by photochemical oxidation of organic precursors of anthropogenic pollutants during transport. The annual average of isotope abundances (δ13C) of OC and EC were -26.9±0.5‰ and -25.6±0.1‰, respectively. There were no notable differences for seasonal distributions of carbon isotopic composition, consistent with motor vehicle emissions being the main source contributors of carbonaceous aerosol in Hong Kong. OC 13C abundances at the regional-scale site were higher than those at the middle-scale roadside and urban sites, consistent with secondary organic aerosols of biogenic origin.

  9. Variability of organic and elemental carbon, water soluble organic carbon, and isotopes in Hong Kong

    NASA Astrophysics Data System (ADS)

    Ho, K. F.; Lee, S. C.; Cao, J. J.; Li, Y. S.; Chow, J. C.; Watson, J. G.; Fung, K.

    2006-06-01

    To determine the levels and variations of carbonaceous aerosol in Hong Kong, PM2.5 and PM10 samples were collected by high volume (Hi-vol) samplers at three monitoring stations (representing middle-scale roadside, urban-, and regional-scale environments) during winter (November 2000 to February 2001) and summer (June 2001 to August 2001) periods. The highest concentrations of organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) were found at the middle-scale roadside site with the lowest at the regional-scale site. The percentages of WSOC in total carbon at these sites were inversely correlated with their concentrations (i.e., the highest percentages of WSOC were observed at the regional-scale site). A high WSOC fraction may be associated with aged aerosol because of the secondary formation by photochemical oxidation of organic precursors of anthropogenic pollutants during transport. The annual average of isotope abundances (δ13C) of OC and EC were -26.9±0.5 and -25.6±0.1, respectively. There were no notable differences for seasonal distributions of carbon isotopic composition, consistent with motor vehicle emissions being the main source contributors of carbonaceous aerosol in Hong Kong. OC 13C abundances at the regional-scale site were higher than those at the middle-scale roadside and urban sites, consistent with secondary organic aerosols of biogenic origin.

  10. Role of fossil fuel and wood burning emissions on Volatile Organic Compounds, Carbon monoxide and Black Carbon level and variability as determined from one-year measurements in Paris.

    NASA Astrophysics Data System (ADS)

    Sarda Esteve, R.; Gros, V.; Kalogridis, A.-C.; Sciare, J.

    2012-04-01

    Within the French program PRIMEQUAL-FRANCIPOL 2010-2013, measurements of gaseous precursors of secondary organic aerosols have been performed at the LHVP (Laboratoire d'Hygiene de la Ville de Paris), an urban background site of Paris. A continuous real-time monitoring strategy using the high sensitivity PTR-MS (Proton Transfer Reaction- Mass Spectrometer) has been implemented for the measurements of Volatile Organic Compounds (VOCs) during a whole year (02/2010-03/2011). The data were acquired in mass-scan mode thus, allowing to follow a very wide range of analytes, namely between m/z 18 and 151. This broad range of compounds includes both well-known VOCs and less studied ones, providing a great exploration potential and the opportunity to establish novel valuable information. This unique dataset will enable to acquire a better understanding of the diurnal, weekday and seasonal trends and to determine the main sources that drive VOCs variability in Paris. The preliminary results herein aim to distinguish the biomass burning from the fuel fossil emissions and to evaluate their impact on the measured volatile organic compounds using tracers Black Carbon (BC) and carbon monoxide (CO). BC was measured and separated into fuel fossil (FF) and wood burning (WB) contributions which can both be used as tracers. The obtained FF contributions to BC are well correlated with measured concentrations of acetaldehyde (m/z 45), acetone (m/z 59), hexanal (m/z 83), probably chloroethane (m/z 85), dimethylbenzene (m/z 107) and trimethylbenzene (TMB) while WB contributions to BC correlate nicely with methanol and the mass 97, maybe related to furfural which has already been identified in smoke from woodburning.

  11. Effect of organic carbon chemistry on sorption of atrazine and metsulfuron-methyl as determined by (13)C-NMR and IR spectroscopy.

    PubMed

    Dutta, Anirban; Mandal, Abhishek; Manna, Suman; Singh, S B; Berns, Anne E; Singh, Neera

    2015-10-01

    Soil organic matter (SOM) content is the major soil component affecting pesticide sorption. However, recent studies have highlighted the fact that it is not the total carbon content of the organic matter, but its chemical structure which have a profound effect on the pesticide's sorption. In the present study, sorption of atrazine and metsulfuron-methyl herbicides was studied in four SOM fractions viz. commercial humic acid, commercial lignin, as well as humic acid and humin extracted from a compost. Sorption data was fitted to the Freundlich adsorption equation. In general, the Freundlich slope (1/n) values for both the herbicides were <1. Except for atrazine sorption on commercial humic acid, metsulfuron-methyl was more sorbed. Desorption results suggested that atrazine was more desorbed than metsulfuron-methyl. Lignin, which showed least sorption of both the herbicides, showed minimum desorption. Sorption of atrazine was best positively correlated with the alkyl carbon (adjusted R (2) = 0.748) and carbonyl carbon (adjusted R (2) = 0.498) but, their effect was statistically nonsignificant (P = 0.05). Metsulfuron-methyl sorption showed best positive correlation with carbonyl carbon (adjusted R (2) = 0.960; P = 0.05) content. Sorption of both the herbicides showed negative correlation with O/N-alkyl carbon. Correlation of herbicide's sorption with alkyl and carbonyl carbon content of SOM fractions suggested their contribution towards herbicide sorption. But, sorption of metsulfuron-methyl, relatively more polar than atrazine, was mainly governed by the polar groups in SOM. IR spectra showed that H-bonds and charge-transfer bonds between SOM fraction and herbicides probably operated as mechanisms of adsorption. PMID:26353968

  12. Determination of organic carbon and ionic accountability of various waste and product waters derived from ECLSS water recovery tests and Spacelab humidity condensate

    NASA Technical Reports Server (NTRS)

    Carter, Donald L.; Cole, Harold; Habercom, Mark; Griffith, Guy

    1992-01-01

    The development of a closed-loop water recovery system for Space Station Freedom involves many technical challenges associated with contaminant removal. Attention is presently given to the characterization of contaminants constituting total organic carbon (TOC), and to the Hubaux and Vos (1970) statistical model for low level TOC that has been employed. A tabulation is given for TOC accountability in the case of both potable and hygiene waters.

  13. Temperature Dependence of Photodegradation of Dissolved Organic Matter to Dissolved Inorganic Carbon and Particulate Organic Carbon

    PubMed Central

    Porcal, Petr; Dillon, Peter J.; Molot, Lewis A.

    2015-01-01

    Photochemical transformation of dissolved organic matter (DOM) has been studied for more than two decades. Usually, laboratory or “in-situ” experiments are used to determine photodegradation variables. A common problem with these experiments is that the photodegradation experiments are done at higher than ambient temperature. Five laboratory experiments were done to determine the effect of temperature on photochemical degradation of DOM. Experimental results showed strong dependence of photodegradation on temperature. Mathematical modeling of processes revealed that two different pathways engaged in photochemical transformation of DOM to dissolved inorganic carbon (DIC) strongly depend on temperature. Direct oxidation of DOM to DIC dominated at low temperatures while conversion of DOM to intermediate particulate organic carbon (POC) prior to oxidation to DIC dominated at high temperatures. It is necessary to consider this strong dependence when the results of laboratory experiments are interpreted in regard to natural processes. Photodegradation experiments done at higher than ambient temperature will necessitate correction of rate constants. PMID:26106898

  14. Determination of carbonate carbon in geological materials by coulometric titration

    USGS Publications Warehouse

    Engleman, E.E.; Jackson, L.L.; Norton, D.R.

    1985-01-01

    A coulometric titration is used for the determination of carbonate carbon in geological materials. Carbon dioxide is evolved from the sample by the addition of 2 M perchloric acid, with heating, and is determined by automated coulometric titration. The coulometric titration showed improved speed and precision with comparable accuracy to gravimetric and gasometric techniques. ?? 1985.

  15. Methods development for total organic carbon accountability

    NASA Technical Reports Server (NTRS)

    Benson, Brian L.; Kilgore, Melvin V., Jr.

    1991-01-01

    This report describes the efforts completed during the contract period beginning November 1, 1990 and ending April 30, 1991. Samples of product hygiene and potable water from WRT 3A were supplied by NASA/MSFC prior to contract award on July 24, 1990. Humidity condensate samples were supplied on August 3, 1990. During the course of this contract chemical analyses were performed on these samples to qualitatively determine specific components comprising, the measured organic carbon concentration. In addition, these samples and known standard solutions were used to identify and develop methodology useful to future comprehensive characterization of similar samples. Standard analyses including pH, conductivity, and total organic carbon (TOC) were conducted. Colorimetric and enzyme linked assays for total protein, bile acid, B-hydroxybutyric acid, methylene blue active substances (MBAS), urea nitrogen, ammonia, and glucose were also performed. Gas chromatographic procedures for non-volatile fatty acids and EPA priority pollutants were also performed. Liquid chromatography was used to screen for non-volatile, water soluble compounds not amenable to GC techniques. Methods development efforts were initiated to separate and quantitate certain chemical classes not classically analyzed in water and wastewater samples. These included carbohydrates, organic acids, and amino acids. Finally, efforts were initiated to identify useful concentration techniques to enhance detection limits and recovery of non-volatile, water soluble compounds.

  16. Potentiometric determination of uranium in organic extracts

    SciTech Connect

    Bodnar, L.Z.

    1980-05-01

    The potentimetric determination of uranium in organic extracts was studied. A mixture of 30% TBP, (tributylphosphate), in carbon tetrachloride was used, with the NBL (New Brunswick Laboratory) titrimetric procedure. Results include a comparative analysis performed on organic extracts of fissium alloys vs those performed on aqueous samples of the same alloys which had been treated to remove interfering elements. Also comparative analyses were performed on sample solutions from a typical scrap recovery operation common in the uranium processing industry. A limited number of residue type materials, calciner products, and presscakes were subjected to analysis by organic extraction. The uranium extraction was not hindered by 30% TBP/CCl/sub 4/. To fully demonstrate the capabilities of the extraction technique and its compatibility with the NBL potentiometric uranium determination, a series of uranium standards was subjected to uranium extraction with 30% TBP/CCl/sub 4/. The uranium was then stripped out of the organic phase with 40 mL of H/sub 3/PO/sub 4/, 15 mL of H/sub 2/0, and 1 mL of 1M FeSO/sub 4/ solution. The uranium was then determined in the aqueous phosphoric phase by the regular NBL potentiometric method, omitting only the addition of another 40 mL of H/sub 3/PO/sub 4/. Uranium determinations ranging from approximately 20 to 150 mg of U were successfully made with the same accuracy and precision normally achieved. 8 tables. (DP)

  17. Investigation of reductive dechlorination supported by natural organic carbon

    USGS Publications Warehouse

    Rectanus, H.V.; Widdowson, M.A.; Chapelle, F.H.; Kelly, C.A.; Novak, J.T.

    2007-01-01

    Because remediation timeframes using monitored natural attenuation may span decades or even centuries at chlorinated solvent sites, new approaches are needed to assess the long-term sustainability of reductive dechlorination in ground water systems. In this study, extraction procedures were used to investigate the mass of indigenous organic carbon in aquifer sediment, and experiments were conducted to determine if the extracted carbon could support reductive dechlorination of chloroethenes. Aquifer sediment cores were collected from a site without an anthropogenic source of organic carbon where organic carbon varied from 0.02% to 0.12%. Single extraction results showed that 1% to 28% of sediment-associated organic carbon and 2% to 36% of the soft carbon were removed depending on nature and concentration of the extracting solution (Nanopure water; 0.1%, 0.5%, and 1.0% sodium pyrophosphate; and 0.5 N sodium hydroxide). Soft carbon is defined as organic carbon oxidized with potassium persulfate and is assumed to serve as a source of biodegradable carbon within the aquifer. Biodegradability studies demonstrated that 20% to 40% of extracted organic carbon was biodegraded aerobically and anaerobically by soil microorganisms in relatively brief tests (45 d). A five-step extraction procedure consisting of 0.1% pyrophosphate and base solutions was investigated to quantify bioavailable organic carbon. Using the extracted carbon as the sole electron donor source, tetrachloroethene was transformed to cis-1,2- dichloroethene and vinyl chloride in anaerobic enrichment culture experiments. Hydrogen gas was produced at levels necessary to sustain reductive dechlorination (>1 nM). ?? 2007 National Ground Water Association.

  18. Organic chemistry of Murchison meteorite: Carbon isotopic fractionation

    NASA Technical Reports Server (NTRS)

    Yuen, G. U.; Blair, N. E.; Desmarais, D. J.; Cronin, J. R.; Chang, S.

    1986-01-01

    The carbon isotopic composition of individual organic compounds of meteoritic origin remains unknown, as most reported carbon isotopic ratios are for bulk carbon or solvent extractable fractions. The researchers managed to determine the carbon isotopic ratios for individual hydrocarbons and monocarboxylic acids isolated from a Murchison sample by a freeze-thaw-ultrasonication technique. The abundances of monocarboxylic acids and saturated hydrocarbons decreased with increasing carbon number and the acids are more abundant than the hydrocarbon with the same carbon number. For both classes of compounds, the C-13 to C-12 ratios decreased with increasing carbon number in a roughly parallel manner, and each carboxylic acid exhibits a higher isotopic number than the hydrocarbon containing the same number of carbon atoms. These trends are consistent with a kinetically controlled synthesis of higher homologues for lower ones.

  19. Simultaneous determination of mercury and organic carbon using a direct mercury analyzer: Mercury profiles in sediment cores from oxbow lakes in the Mississippi Delta

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Sediment cores from seasonal wetland and open water areas from six oxbow lakes in the Mississippi River alluvial flood plain were analyzed for total-mercury (Hg) using a direct mercury analyzer (DMA). In the process we evaluated the feasibility of simultaneously determining organic matter content by...

  20. METHOD 415.3 - MEASUREMENT OF TOTAL ORGANIC CARBON, DISSOLVED ORGANIC CARBON AND SPECIFIC UV ABSORBANCE AT 254 NM IN SOURCE WATER AND DRINKING WATER

    EPA Science Inventory

    2.0 SUMMARY OF METHOD

    2.1 In both TOC and DOC determinations, organic carbon in the water sample is oxidized to form carbon dioxide (CO2), which is then measured by a detection system. There are two different approaches for the oxidation of organic carbon in water sample...

  1. Carbon nanotube electrodes in organic transistors.

    PubMed

    Valitova, Irina; Amato, Michele; Mahvash, Farzaneh; Cantele, Giovanni; Maffucci, Antonio; Santato, Clara; Martel, Richard; Cicoira, Fabio

    2013-06-01

    The scope of this Minireview is to provide an overview of the recent progress on carbon nanotube electrodes applied to organic thin film transistors. After an introduction on the general aspects of the charge injection processes at various electrode-semiconductor interfaces, we discuss the great potential of carbon nanotube electrodes for organic thin film transistors and the recent achievements in the field. PMID:23639944

  2. 42 CFR 422.566 - Organization determinations.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 42 Public Health 3 2014-10-01 2014-10-01 false Organization determinations. 422.566 Section 422... (CONTINUED) MEDICARE PROGRAM (CONTINUED) MEDICARE ADVANTAGE PROGRAM Grievances, Organization Determinations and Appeals § 422.566 Organization determinations. (a) Responsibilities of the MA organization....

  3. 42 CFR 422.566 - Organization determinations.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 42 Public Health 3 2013-10-01 2013-10-01 false Organization determinations. 422.566 Section 422... (CONTINUED) MEDICARE PROGRAM (CONTINUED) MEDICARE ADVANTAGE PROGRAM Grievances, Organization Determinations and Appeals § 422.566 Organization determinations. (a) Responsibilities of the MA organization....

  4. Determination of Total Petroleum Hydrocarbons (TPH) Using Total Carbon Analysis

    SciTech Connect

    Ekechukwu, A.A.

    2002-05-10

    Several methods have been proposed to replace the Freon(TM)-extraction method to determine total petroleum hydrocarbon (TPH) content. For reasons of cost, sensitivity, precision, or simplicity, none of the replacement methods are feasible for analysis of radioactive samples at our facility. We have developed a method to measure total petroleum hydrocarbon content in aqueous sample matrixes using total organic carbon (total carbon) determination. The total carbon content (TC1) of the sample is measured using a total organic carbon analyzer. The sample is then contacted with a small volume of non-pokar solvent to extract the total petroleum hydrocarbons. The total carbon content of the resultant aqueous phase of the extracted sample (TC2) is measured. Total petroleum hydrocarbon content is calculated (TPH = TC1-TC2). The resultant data are consistent with results obtained using Freon(TM) extraction followed by infrared absorbance.

  5. Worldwide organic soil carbon and nitrogen data

    SciTech Connect

    Zinke, P.J.; Stangenberger, A.G.; Post, W.M.; Emanual, W.R.; Olson, J.S.

    1986-09-01

    The objective of the research presented in this package was to identify data that could be used to estimate the size of the soil organic carbon pool under relatively undisturbed soil conditions. A subset of the data can be used to estimate amounts of soil carbon storage at equilibrium with natural soil-forming factors. The magnitude of soil properties so defined is a resulting nonequilibrium values for carbon storage. Variation in these values is due to differences in local and geographic soil-forming factors. Therefore, information is included on location, soil nitrogen content, climate, and vegetation along with carbon density and variation.

  6. Organic solvent regeneration of granular activated carbon

    NASA Astrophysics Data System (ADS)

    Cross, W. H.; Suidan, M. T.; Roller, M. A.; Kim, B. R.; Gould, J. P.

    1982-09-01

    The use of activated carbon for the treatment of industrial waste-streams was shown to be an effective treatment. The high costs associated with the replacement or thermal regeneration of the carbon have prohibited the economic feasibility of this process. The in situ solvent regeneration of activated carbon by means of organic solvent extraction was suggested as an economically alternative to thermal regeneration. The important aspects of the solvent regeneration process include: the physical and chemical characteristics of the adsorbent, the pore size distribution and energy of adsorption associated with the activated carbon; the degree of solubility of the adsorbate in the organic solvent; the miscibility of the organic solvent in water; and the temperature at which the generation is performed.

  7. 42 CFR 422.566 - Organization determinations.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 42 Public Health 3 2011-10-01 2011-10-01 false Organization determinations. 422.566 Section 422.566 Public Health CENTERS FOR MEDICARE & MEDICAID SERVICES, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICARE PROGRAM MEDICARE ADVANTAGE PROGRAM Grievances, Organization Determinations and Appeals § 422.566 Organization determinations....

  8. Organic carbon biostimulates rapid rhizodegradation of perchlorate.

    PubMed

    Yifru, Dawit D; Nzengung, Valentine A

    2008-12-01

    Previous hydroponics and field studies identified phytodegradation and rhizodegradation as the two main mechanisms by which plants metabolize perchlorate. Plant uptake and phytodegradation of perchlorate is a slower and undesired process that poses ecological risks resulting from phytoaccumulation of some fraction of the perchlorate. Meanwhile, rhizodegradation is a more rapid and favored process involving perchlorate-degrading bacteria utilizing dissolved organic carbon (DOC) as a carbon and energy (electron) source to rapidly degrade perchlorate to innocuous chloride. In the present study, rhizodegradation of perchlorate by willow trees (Salix nigra) was biostimulated using electron sources obtained from natural and artificial carbon sources. In bioreactors provided with carbon sources as 500 mg/L DOC, 25 to 40 mg/L of initial perchlorate concentrations were removed to below the ion chromatography method detection limit of 2 microg/L in approximately 9 d. For planted controls provided with no electron donors, the time required for the complete removal of the same doses of perchlorate was up to 70 d. Enhancement of rhizodegradation by organic carbon reduced the phytoaccumulated fraction of perchlorate by an order of magnitude from approximately 430 to 20 mg/kg. The implication of the present study is that the high fraction uptake and phytoaccumulation of perchlorate in agricultural products and the recycling of perchlorate into the ecosystem can be significantly curtailed by supplying electron donors derived from organic carbon sources to the root zone of plants. PMID:18593217

  9. Organic carbon burial efficiency in a large tropical hydroelectric reservoir

    NASA Astrophysics Data System (ADS)

    Mendonça, Raquel; Sobek, Sebastian; Kosten, Sarian; Cole, Jonathan; Cardoso, Simone; Roland, Fábio

    2014-05-01

    Because hydroelectric reservoirs receive relatively high inputs of sediments when compared to lakes and oceans, these systems are important sites for organic carbon (OC) accumulation. Nevertheless, the actual magnitude of carbon accumulating in reservoirs is poorly known due to a lack of whole-system studies of carbon burial. Hydroelectric reservoirs are also particularly heterogeneous systems in terms of organic carbon sources and sedimentation rates. Such heterogeneity leads to strong variations on carbon fluxes, even though the effect on OC burial has not yet been discussed. The aim of this paper was to determine the OC burial rate and efficiency in a large tropical reservoir and evaluate the importance of spatial heterogeneity affecting OC burial. Burial rates were determined through a novel approach which combines sediment sample analyses and a seismic survey. Our results confirm the major effect of sedimentation heterogeneity on OC burial efficiency which varied from 9 to 89% in the reservoir. In addition to the river-dam gradient of sedimentation, our data reinforce the importance of basin morphometry in determining the patterns of sediment deposition and carbon accumulation. No carbon accumulation occurred along the margins of the reservoir and irregular bottom morphology leaded to irregular carbon deposition. An integrative analysis, including the reservoir's heterogeneity, indicated that the whole system accumulates 42.2 g C m-2 yr-1 and that roughly 67% of the total OC load to the sediments is actually buried. The data also suggest that the sediment of the reservoir is mainly composed of terrestrial OC and that the heterogeneity in OC sources plays a minor role determining OC burial efficiency, which was strongly determined by sediment accumulation rate. Finally, our results in combination with literature data suggest that the high sedimentation rates cause hydroelectric reservoirs to accumulate carbon more efficiently than lakes, regardless of

  10. Carbon aging mechanisms and effects on retention of organic iodides

    SciTech Connect

    Hyder, M.L.

    1985-01-01

    The activated carbon used to treat the off-gas from the Savannah River Plant prodution reactor building was studied to determine the chemical changes occurring in this carbon during its service life. The carbon is a coconut-shell charcoal impregnated with 1% triethylenediamine (TEDA) and 2% KI. It was known that during its 30-month service life the carbon becomes more acidic and less effective for retaining iodine in organic form. The study showed that the most important change occurring in the carbon is the reaction of KI to give other chemical forms of iodine. The reacted iodine is unavailable for exchange with alkyl iodides. The results suggest that the carbon reacts with KI to form organic compounds, but small amounts of oxidized iodine may also be presnt. There is also evidence that some iodide is lost from the carbon altogether. The TEDA impregnant is lost from the carbon very quickly, and has no importance after a few months. The specific reactions by which the impregnant is lost have not been identified. However, mathematical analysis shows that the carbon performance data are consistent with the reaction of iodide impregnant with impurities in the air flowing through the carbon bed. Additional mathematical analysis, based on electron microscopic observation of the carbon particles, indicates that the external surfaces of the carbon are mainly responsible for their effectiveness in retaining iodine. Consequently, the condition of the impregnants on a relatively small fraction of the carbon surface can have a large effect on its performance. 4 refs., 14 figs., 2 tabs.

  11. Fertilization increases paddy soil organic carbon density*

    PubMed Central

    Wang, Shao-xian; Liang, Xin-qiang; Luo, Qi-xiang; Fan, Fang; Chen, Ying-xu; Li, Zu-zhang; Sun, Huo-xi; Dai, Tian-fang; Wan, Jun-nan; Li, Xiao-jun

    2012-01-01

    Field experiments provide an opportunity to study the effects of fertilization on soil organic carbon (SOC) sequestration. We sampled soils from a long-term (25 years) paddy experiment in subtropical China. The experiment included eight treatments: (1) check, (2) PK, (3) NP, (4) NK, (5) NPK, (6) 7F:3M (N, P, K inorganic fertilizers+30% organic N), (7) 5F:5M (N, P, K inorganic fertilizers+50% organic N), (8) 3F:7M (N, P, K inorganic fertilizers+70% organic N). Fertilization increased SOC content in the plow layers compared to the non-fertilized check treatment. The SOC density in the top 100 cm of soil ranged from 73.12 to 91.36 Mg/ha. The SOC densities of all fertilizer treatments were greater than that of the check. Those treatments that combined inorganic fertilizers and organic amendments had greater SOC densities than those receiving only inorganic fertilizers. The SOC density was closely correlated to the sum of the soil carbon converted from organic amendments and rice residues. Carbon sequestration in paddy soils could be achieved by balanced and combined fertilization. Fertilization combining both inorganic fertilizers and organic amendments is an effective sustainable practice to sequestrate SOC. PMID:22467369

  12. Effect of some organic solvent-water mixtures composition on precipitated calcium carbonate in carbonation process

    NASA Astrophysics Data System (ADS)

    Konopacka-Łyskawa, Donata; Kościelska, Barbara; Karczewski, Jakub

    2015-05-01

    Precipitated calcium carbonate particles were obtained during carbonation of calcium hydroxide slurry with carbon dioxide. Aqueous solutions of isopropyl alcohol, n-butanol and glycerol were used as solvents. Concentration of organic additives in the reactive mixture was from 0% to 20% (vol). Precipitation process were performed in a stirred tank reactor equipped with gas distributor. Multimodal courses of particles size distribution were determined for produced CaCO3 particles. Calcium carbonate as calcite was precipitated in all experiments. The mean Sauter diameter of CaCO3 particles decreased when the concentration of all used organic additives increased. The amount of small particle fraction in the product increased with the increasing concentration of organic solvents. Similar physical properties of used liquid phase resulted in the similar characteristics of obtained particles.

  13. How to Enhance Soil Organic Carbon Sequestration

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Optimizing crop yields and reducing soil erosion can enhance soil organic carbon (SOC) sequestration. The influence of management practices on crop residue C and N inputs to the soil, SOC sequestration, and NO3-N leaching potential under irrigated, continuous crop production in northern Texas was e...

  14. CARBON ADSORPTION ISOTHERMS FOR TOXIC ORGANICS

    EPA Science Inventory

    An experimental protocol for measuring the activated carbon adsorption isotherm was developed and applied to a wide range of organic compounds. Methods for treatment of the isotherm data and a standard format for presentation of results are shown. In the early phase of the study ...

  15. 42 CFR 417.838 - Organization determinations.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 42 Public Health 3 2011-10-01 2011-10-01 false Organization determinations. 417.838 Section 417... (CONTINUED) MEDICARE PROGRAM HEALTH MAINTENANCE ORGANIZATIONS, COMPETITIVE MEDICAL PLANS, AND HEALTH CARE PREPAYMENT PLANS Health Care Prepayment Plans § 417.838 Organization determinations. (a) Actions that...

  16. 42 CFR 417.838 - Organization determinations.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 42 Public Health 3 2010-10-01 2010-10-01 false Organization determinations. 417.838 Section 417... (CONTINUED) MEDICARE PROGRAM HEALTH MAINTENANCE ORGANIZATIONS, COMPETITIVE MEDICAL PLANS, AND HEALTH CARE PREPAYMENT PLANS Health Care Prepayment Plans § 417.838 Organization determinations. (a) Actions that...

  17. Subduction of Organic Carbon into the Earth

    NASA Astrophysics Data System (ADS)

    Plank, T. A.; Malinverno, A.

    2015-12-01

    Seafloor sediments approach active subduction zones with small amounts (generally < 1 dry weight %) of organic carbon, but this small concentration nonetheless constitutes a significant flux over geological time with respect to the size, isotopic composition and electron balance of the carbosphere. In order to quantify the flux of organic carbon into subduction zones, we have examined carbon concentration and density measurements provided by successive drilling programs (DSDP, ODP, IODP) for cores that sample complete sediment sections to basement near deep sea trenches. An interpolation scheme compensates for sparse or non-uniform analyses, and a weighted bulk concentration is calculated for organic carbon (OC) and inorganic carbonate (IC) for each site. When multiplied by the sediment thickness, the trench length and the convergence velocity, a subducted mass flux can be obtained. Sites with the greatest concentration of OC include those that pass beneath regions of high biological productivity (such as the Eastern Equatorial Pacific) and those that receive terrigenous turbidites (e.g., Indus and Begal Fans, Gulf of Alaska, Cascadia, etc). Together, terrigenous turbidites make up about 60% of the global subducted sediment (GLOSS), and thus have a strong control on the concentration of OC in GLOSS. Sites dominated by terrigenous turbidites have 0.4 wt% OC on average (1sd = 0.1 wt%), and GLOSS is very similar, yielding about 6 MtC/yr OC subducted globally. This flux is enough to subduct the entire surface pool of OC every 2.6 Ga, which if not returned, or returned in a more oxidized form, could contribute to a significant rise in oxygen at the surface of the Earth. Seemingly fortuitously, the OC/total carbon fraction in GLOSS is 20%, very near the long term average required to maintain the isotopic composition of marine carbonates at ~ 0 per mil d13C over much of Earth history.

  18. Yucca Mountain Area Saturated Zone Dissolved Organic Carbon Isotopic Data

    SciTech Connect

    Thomas, James; Decker, David; Patterson, Gary; Peterman, Zell; Mihevc, Todd; Larsen, Jessica; Hershey, Ronald

    2007-06-25

    Groundwater samples in the Yucca Mountain area were collected for chemical and isotopic analyses and measurements of water temperature, pH, specific conductivity, and alkalinity were obtained at the well or spring at the time of sampling. For this project, groundwater samples were analyzed for major-ion chemistry, deuterium, oxygen-18, and carbon isotopes of dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC). The U.S. Geological Survey (USGS) performed all the fieldwork on this project including measurement of water chemistry field parameters and sample collection. The major ions dissolved in the groundwater, deuterium, oxygen-18, and carbon isotopes of dissolved inorganic carbon (DIC) were analyzed by the USGS. All preparation and processing of samples for DOC carbon isotopic analyses and geochemical modeling were performed by the Desert Research Institute (DRI). Analysis of the DOC carbon dioxide gas produced at DRI to obtain carbon-13 and carbon-14 values was conducted at the University of Arizona Accelerator Facility (a NSHE Yucca Mountain project QA qualified contract facility). The major-ion chemistry, deuterium, oxygen-18, and carbon isotopes of DIC were used in geochemical modeling (NETPATH) to determine groundwater sources, flow paths, mixing, and ages. The carbon isotopes of DOC were used to calculate groundwater ages that are independent of DIC model corrected carbon-14 ages. The DIC model corrected carbon-14 calculated ages were used to evaluate groundwater travel times for mixtures of water including water beneath Yucca Mountain. When possible, groundwater travel times were calculated for groundwater flow from beneath Yucca Mountain to down gradient sample sites. DOC carbon-14 groundwater ages were also calculated for groundwaters in the Yucca Mountain area. When possible, groundwater travel times were estimated for groundwater flow from beneath Yucca Mountain to down gradient groundwater sample sites using the DOC calculated

  19. Organic carbon transport in the Columbia River

    NASA Astrophysics Data System (ADS)

    Dahm, Clifford N.; Gregory, Stanley V.; Kilho Park, P.

    1981-12-01

    Total organic carbon (TOC) levels in the Columbia River measured monthly from May 1973 to December 1974 ranged from a maximum of 270 μmol l -1 during late spring and early summer to a minimum of 150 μmol l -1 during late autumn. Sampling locations were directly behind the spillway at the Bonneville Dam, 230 km upstream, and at Kalama, Washington, 128km upstream from the river mouth. The average annual TOC contribution from the Columbia River drainage to the north-eastern Pacific is 4·9×10 10 mol with an average concentration of approximately 195μmol l -1. Of this TOC annual export, 89% is dissolved organic carbon (DOC) and 11% is particulate organic carbon (OOC). The TOC and DOC levels were most highly correlated with increased oxygen saturation and dischange, while POC correlated more closely to high instream primary productivy as indicated by higher pH and oxygen supersaturation. Variability of DOC in the main channel of the Columbia River from Portland, Oregon, to the estuary during a June 1974 cruise was minimal. The DOC concentrations ranged from 221-260 μmol l -1 with no significant upstream or downstream gradients. Diel variation also was slight, varying randomly during 24h between 235-257 μmol l -1. The relative annual constancy of the DOC is indicative of the refractory nature of a significant proportion of the dissolved organic load of the Columbia River.

  20. Remote Sensing to Support Monitoring of Soil Organic Carbon (Invited)

    NASA Astrophysics Data System (ADS)

    McNairn, H.; Pacheco, A.

    2009-12-01

    Soil organic carbon is fundamental to the sustainability of agricultural soils and soils play an important role in the global carbon balance. Estimating soil carbon levels and monitoring changes in these levels over time requires extensive data on climate, soil properties, land cover and land management. Remote sensing technologies are capable of providing some of the data needed in modeling soil organic carbon concentrations and in tracking changes in soil carbon. The characteristics of the vegetation cover influence the amount of organic matter in the soil and cultivation impacts the rate of organic matter decomposition. Consequently land management decisions, which include cropping and tillage practices, play a vital role in determining soil carbon levels. Agriculture and Agri-Food Canada (AAFC) has developed several methods to map land management practices from multispectral and Synthetic Aperture Radar (SAR) satellite sensors. These include identification of crops grown, estimation of crop residue cover left post-harvest and identification of tillage activities. Optical and SAR data are capable of identifying crop types to accuracies consistently above 85%. Knowledge of crop type also provides information needed to establish biomass levels and residue type, both of which influence the amounts and decomposition rates of organic matter. Scientists with AAFC have also extensively validated a method to estimate percent residue cover using spectral unmixing analysis applied to multispectral satellite data. Percentages for corn, soybean and small grain residues can be estimated to accuracies of 83%, 80% and 82%, respectively. Tillage activity influences residue decomposition and AAFC is investigating methods to identify tillage occurrence using advanced polarimetric SAR information. This presentation will provide an overview of methods and results from research ongoing at AAFC. The potential contribution of these remote sensing approaches to support wide area carbon

  1. [Effects of different fertilizer application on soil active organic carbon].

    PubMed

    Zhang, Rui; Zhang, Gui-Long; Ji, Yan-Yan; Li, Gang; Chang, Hong; Yang, Dian-Lin

    2013-01-01

    The variation characteristics of the content and components of soil active organic carbon under different fertilizer application were investigated in samples of calcareous fluvo-aquic soil from a field experiment growing winter wheat and summer maize in rotation in the North China Plain. The results showed that RF (recommended fertilization), CF (conventional fertilization) and NPK (mineral fertilizer alone) significantly increased the content of soil dissolved organic carbon and easily oxidized organic carbon by 24.92-38.63 mg x kg(-1) and 0.94-0.58 mg x kg(-1) respectively compared to CK (unfertilized control). The soil dissolved organic carbon content under OM (organic manure) increased greater than those under NPK and single fertilization, soil easily oxidized organic carbon content under OM and NPK increased greater than that under single chemical fertilization. OM and NPK showed no significant role in promoting the soil microbial biomass carbon, but combined application of OM and NPK significantly increased the soil microbial biomass carbon content by 36.06% and 20.69%, respectively. Soil easily oxidized organic carbon, dissolved organic carbon and microbial biomass carbon accounted for 8.41% - 14.83%, 0.47% - 0.70% and 0.89% - 1.20% of the total organic carbon (TOC), respectively. According to the results, the fertilizer application significantly increased the proportion of soil dissolved organic carbon and easily oxidized organic carbon, but there was no significant difference in the increasing extent of dissolved organic carbon. The RF and CF increased the proportion of soil easily oxidized organic carbon greater than OM or NPK, and significantly increased the proportion of microbial biomass carbon. OM or RF had no significant effect on the proportion of microbial biomass carbon. Therefore, in the field experiment, appropriate application of organic manure and chemical fertilizers played an important role for the increase of soil active organic carbon

  2. 42 CFR 422.566 - Organization determinations.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 42 Public Health 3 2012-10-01 2012-10-01 false Organization determinations. 422.566 Section 422.566 Public Health CENTERS FOR MEDICARE & MEDICAID SERVICES, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICARE PROGRAM (CONTINUED) MEDICARE ADVANTAGE PROGRAM Grievances, Organization Determinations and Appeals § 422.566...

  3. Cost effective tools for soil organic carbon monitoring

    NASA Astrophysics Data System (ADS)

    Shepherd, Keith; Aynekulu, Ermias

    2013-04-01

    There is increasing demand for data on soil properties at fine spatial resolution to support management and planning decisions. Measurement of soil organic carbon has attracted much interest because (i) soil organic carbon is widely cited as a useful indicator of soil condition and (ii) of the importance of soil carbon in the global carbon cycle and climate mitigation strategies. However in considering soil measurement designs there has been insufficient attention given to careful analysis of the specific decisions that the measurements are meant to support and on what measurements have high information value for decision-making. As a result, much measurement effort may be wasted or focused on the wrong variables. A cost-effective measurement is one that reduces risk in decisions and does not cost more than the societal returns to additional evidence. A key uncertainty in measuring soil carbon as a soil condition indicator is what constitutes a good or bad level of carbon on a given soil. A measure of soil organic carbon concentration may have limited value for informing management decisions without the additional information required to interpret it, and so expending further efforts on improving measurements to increase precision may then have no value to improving the decision. Measuring soil carbon stock changes for carbon trading purposes requires high levels of measurement precision but there is still large uncertainty on whether the costs of measurement exceed the benefits. Since the largest cost component in soil monitoring is often travel to the field and physically sampling soils, it is generally cost-effective to meet multiple objectives by analysing a number of properties on a soil sample. Diffuse reflectance infrared spectroscopy is playing a key role in allowing multiple soil properties to be determined rapidly and at low cost. The method provides estimation of multiple soil properties (e.g. soil carbon, texture and mineralogy) in one measurement

  4. Black Carbon Contribution to Organic Carbon Stocks in Urban Soil.

    PubMed

    Edmondson, Jill L; Stott, Iain; Potter, Jonathan; Lopez-Capel, Elisa; Manning, David A C; Gaston, Kevin J; Leake, Jonathan R

    2015-07-21

    Soil holds 75% of the total organic carbon (TOC) stock in terrestrial ecosystems. This comprises ecosystem-derived organic carbon (OC) and black carbon (BC), a recalcitrant product of the incomplete combustion of fossil fuels and biomass. Urban topsoils are often enriched in BC from historical emissions of soot and have high TOC concentrations, but the contribution of BC to TOC throughout the urban soil profile, at a regional scale is unknown. We sampled 55 urban soil profiles across the North East of England, a region with a history of coal burning and heavy industry. Through combined elemental and thermogravimetic analyses, we found very large total soil OC stocks (31-65 kg m(-2) to 1 m), exceeding typical values reported for UK woodland soils. BC contributed 28-39% of the TOC stocks, up to 23 kg C m(-2) to 1 m, and was affected by soil texture. The proportional contribution of the BC-rich fraction to TOC increased with soil depth, and was enriched in topsoil under trees when compared to grassland. Our findings establish the importance of urban ecosystems in storing large amounts of OC in soils and that these soils also capture a large proportion of BC particulates emitted within urban areas. PMID:26114917

  5. Soil Organic Carbon Loss: An Overlooked Factor in the Carbon Sequestration Potential of Enhanced Mineral Weathering

    NASA Astrophysics Data System (ADS)

    Dietzen, Christiana; Harrison, Robert

    2016-04-01

    Weathering of silicate minerals regulates the global carbon cycle on geologic timescales. Several authors have proposed that applying finely ground silicate minerals to soils, where organic acids would enhance the rate of weathering, could increase carbon uptake and mitigate anthropogenic CO2 emissions. Silicate minerals such as olivine could replace lime, which is commonly used to remediate soil acidification, thereby sequestering CO2 while achieving the same increase in soil pH. However, the effect of adding this material on soil organic matter, the largest terrestrial pool of carbon, has yet to be considered. Microbial biomass and respiration have been observed to increase with decreasing acidity, but it is unclear how long the effect lasts. If the addition of silicate minerals promotes the loss of soil organic carbon through decomposition, it could significantly reduce the efficiency of this process or even create a net carbon source. However, it is possible that this initial flush of microbial activity may be compensated for by additional organic matter inputs to soil pools due to increases in plant productivity under less acidic conditions. This study aimed to examine the effects of olivine amendments on soil CO2 flux. A liming treatment representative of typical agricultural practices was also included for comparison. Samples from two highly acidic soils were split into groups amended with olivine or lime and a control group. These samples were incubated at 22°C and constant soil moisture in jars with airtight septa lids. Gas samples were extracted periodically over the course of 2 months and change in headspace CO2 concentration was determined. The effects of enhanced mineral weathering on soil organic matter have yet to be addressed by those promoting this method of carbon sequestration. This project provides the first data on the potential effects of enhanced mineral weathering in the soil environment on soil organic carbon pools.

  6. Site-Specific Carbon Isotopes in Organics

    NASA Astrophysics Data System (ADS)

    Piasecki, A.; Eiler, J. M.

    2012-12-01

    Natural organic molecules exhibit a wide range of internal site-specific isotope variation (i.e., molecules with same isotopic substitution type but different site). Such variations are generally unconstrained by bulk isotopic measurements. If known, site-specific variations might constrain temperatures of equilibrium, mechanisms of formation or consumption reactions, and possibly other details. For example, lipids can exhibit carbon isotope differences of up to 30‰ between adjacent carbon sites as a result of fractionations arising during decarboxylation of pyruvate and other steps in lipid biosynthesis(1). We present a method for site-specific carbon isotope analysis of propane, based on high-resolution, multi-collector gas source mass spectrometry, using a novel prototype instrument - the Thermo MAT 253 Ultra. This machine has an inlet system and electron bombardment ion source resembling those in conventional stable isotope gas source mass spectrometers, and the energy filter, magnet, and detector array resembling those in multi-collector ICPMS and TIMS. The detector array has 7 detector positions, 6 of which are movable, and each of which can collect ions with either a faraday cup (read through amplifiers ranging from 107-1012 ohms) or an SEM. High mass resolving power (up to 27,000, MRP = M/dM definition) is achieved through a narrow entrance slit, adjustable from 250 to 5 μm. Such resolution can cleanly separate isobaric interferences between isotopologues of organic molecules having the same cardinal mass (e.g., 13CH3 and 12CH2D). We use this technology to analyze the isotopologues and fragments of propane, and use such data to solve for the site-specific carbon isotope fractionation. By measuring isotopologues of both the one-carbon (13CH3) and the two-carbon (13C12CH4) fragment ion, we can solve for both bulk δ13C and the difference in δ13C between the terminal and central carbon position. We tested this method by analyzing mixtures between natural

  7. Epitaxial Approaches to Carbon Nanotube Organization

    NASA Astrophysics Data System (ADS)

    Ismach, Ariel

    Carbon nanotubes have unique electronic, mechanical, optical and thermal properties, which make them ideal candidates as building blocks in nano-electronic and electromechanical systems. However, their organization into well-defined geometries and arrays on surfaces remains a critical challenge for their integration into functional nanosystems. In my PhD, we developed a new approach for the organization of carbon nanotubes directed by crystal surfaces. The principle relies on the guided growth of single-wall carbon nanotubes (SWNTs) by atomic features presented on anisotropic substrates. We identified three different modes of surface-directed growth (or 'nanotube epitaxy'), in which the growth of carbon nanotubes is directed by crystal substrates: We first observed the nanotube unidirectional growth along atomic steps ('ledge-directed epitaxy') and nanofacets ('graphoepitaxy') on the surface of miscut C-plane sapphire and quartz. The orientation along crystallographic directions ('lattice-directed epitaxy') was subsequently observed by other groups on different crystals. We have proposed a "wake growth" mechanism for the nanotube alignment along atomic steps and nanofacets. In this mechanism, the catalyst nanoparticle slides along the step or facet, leaving the nanotube behind as a wake. In addition, we showed that the combination of surface-directed growth with external forces, such as electric-field and gas flow, can lead to the simultaneous formation of complex nanotube structures, such as grids and serpentines. The "wake growth" model, which explained the growth of aligned nanotubes, could not explain the formation of nanotube serpentines. For the latter, we proposed a "falling spaghetti" mechanism, in which the nanotube first grows by a free-standing process, aligned in the direction of the gas flow, then followed by absorption on the stepped surface in an oscillatory manner, due to the competition between the drag force caused by the gas flow on the suspended

  8. Urban Tree Effects on Soil Organic Carbon

    PubMed Central

    Edmondson, Jill L.; O'Sullivan, Odhran S.; Inger, Richard; Potter, Jonathan; McHugh, Nicola; Gaston, Kevin J.; Leake, Jonathan R.

    2014-01-01

    Urban trees sequester carbon into biomass and provide many ecosystem service benefits aboveground leading to worldwide tree planting schemes. Since soils hold ∼75% of ecosystem organic carbon, understanding the effect of urban trees on soil organic carbon (SOC) and soil properties that underpin belowground ecosystem services is vital. We use an observational study to investigate effects of three important tree genera and mixed-species woodlands on soil properties (to 1 m depth) compared to adjacent urban grasslands. Aboveground biomass and belowground ecosystem service provision by urban trees are found not to be directly coupled. Indeed, SOC enhancement relative to urban grasslands is genus-specific being highest under Fraxinus excelsior and Acer spp., but similar to grasslands under Quercus robur and mixed woodland. Tree cover type does not influence soil bulk density or C∶N ratio, properties which indicate the ability of soils to provide regulating ecosystem services such as nutrient cycling and flood mitigation. The trends observed in this study suggest that genus selection is important to maximise long-term SOC storage under urban trees, but emerging threats from genus-specific pathogens must also be considered. PMID:25003872

  9. Urban tree effects on soil organic carbon.

    PubMed

    Edmondson, Jill L; O'Sullivan, Odhran S; Inger, Richard; Potter, Jonathan; McHugh, Nicola; Gaston, Kevin J; Leake, Jonathan R

    2014-01-01

    Urban trees sequester carbon into biomass and provide many ecosystem service benefits aboveground leading to worldwide tree planting schemes. Since soils hold ∼75% of ecosystem organic carbon, understanding the effect of urban trees on soil organic carbon (SOC) and soil properties that underpin belowground ecosystem services is vital. We use an observational study to investigate effects of three important tree genera and mixed-species woodlands on soil properties (to 1 m depth) compared to adjacent urban grasslands. Aboveground biomass and belowground ecosystem service provision by urban trees are found not to be directly coupled. Indeed, SOC enhancement relative to urban grasslands is genus-specific being highest under Fraxinus excelsior and Acer spp., but similar to grasslands under Quercus robur and mixed woodland. Tree cover type does not influence soil bulk density or C∶N ratio, properties which indicate the ability of soils to provide regulating ecosystem services such as nutrient cycling and flood mitigation. The trends observed in this study suggest that genus selection is important to maximise long-term SOC storage under urban trees, but emerging threats from genus-specific pathogens must also be considered. PMID:25003872

  10. Terrestrial organic carbon contributions to sediments on the Washington margin

    SciTech Connect

    Prahl, F.G.; Sparrow, M.A.; Eversmeyer, B. ); Ertel, J.R. ); Goni, M.A. )

    1994-07-01

    Elemental and stable carbon isotopic compositions and biomarker concentrations were determined in sediments from the Columbia River basin and the Washington margin in order to evaluate geochemical approaches for quantifying terrestrial organic matter in marine sediments. The biomarkers include: an homologous series of long-chain n-alkanes derived from the surface waxes of higher plants; phenolic and hydroxyalkanoic compounds produced by CuO oxidation of two major vascular plant biopolymers, lignin and cutin. All marine sediments, including samples collected from the most remote sites in Cascadia Basin, showed organic geochemical evidence for the presence of terrestrial organic carbon. Using endmember values for the various biomarkers determined empirically by two independent means, the authors estimate that the terrestrial contribution to the Washington margin is [approximately] 60% for shelf sediments, [approximately] 30% for slope sediments, and decreases further to [le] 15% in basin sediments. Results from the same geochemical measurements made with depth in gravity core 6705-7 from Cascadia Seachannel suggest that this approach to assess terrestrial organic carbon contributions to contemporary deposits on the Washington margin can be applied to the study of sediments depositing in this region since the last glacial period.

  11. Gravimetric Determination of Inorganic Carbon in Calcareous Soils Using the Carbonate-Meter

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Organic carbon affects many important physical, chemical and microbiological soil properties. In calcareous soils, the inorganic carbon has to be measured and subtracted from the total carbon to obtain organic carbon. Our objective was to develop a gravimetric technique to quantify inorganic carbon ...

  12. Green Carbon, Black Carbon, White Carbon: Simultaneous Differentiation Between Soil Organic Matter, Pyrogenic Carbon and Carbonates Using Thermal Analysis Techniques

    NASA Astrophysics Data System (ADS)

    Plante, A. F.; Peltre, C.; Chan, J.; Baumgartl, T.; Erskine, P.; Apesteguía, M.; Virto, I.

    2014-12-01

    Quantification of soil carbon stocks and fluxes continues to be an important endeavor in assessments of soil quality, and more broadly in assessments of ecosystem functioning. The quantification of soil carbon in alkaline, carbonate-containing soils, such as those found in Mediterranean areas, is complicated by the need to differentiate between organic carbon (OC) and inorganic carbon (IC), which continues to present methodological challenges. Acidification is frequently used to eliminate carbonates prior to soil OC quantification, but when performed in the liquid phase, can promote the dissolution and loss of a portion of the OC. Acid fumigation (AF) is increasingly preferred for carbonate removal, but its effectiveness is difficult to assess using conventional elemental and isotopic analyses. The two-step approach is time, labor and cost intensive, and generates additional uncertainties from the calculations. Quantification of the actively cycling pool of soil organic C (SOC) in many soils is further complicated by the potential presence of more recalcitrant/stable forms such as pyrogenic or black carbon (BC) derived from incomplete combustion of vegetation, or even geogenic carbon such as coal. The wide spectrum of materials currently considered BC makes its quantification challenging. The chemical method using benzene polycarboxylic acids (BPCAs) as markers of condensed aromatic structures indicative of pyrogenic C is highly time, labor and cost intensive, and can generate artifacts. Several research groups are now developing method for the simultaneous identification and quantification of these various forms of soil carbon using thermal analysis techniques such as thermogravimetry, differential scanning calorimetry and evolved gas analysis. The objective of this presentation is to provide a general overview and specific examples of the current progress and technical challenges in this evolving methodology.

  13. Primary and Secondary Organic Carbon Downwind of Mexico City

    SciTech Connect

    Yu, Xiao-Ying; Cary, R.; Laulainen, Nels S.

    2009-09-18

    In order to study particulate matter transport and transformation in the Megacity environment, fine particulate carbons were measured simultaneously at two supersites, suburban T1 and rural T2, downwind of Mexico City during the MILAGRO field campaign in March 2006. Organic carbon (OC), element carbon (EC), and total carbon (TC=OC+EC) were determined near real-time by the Sunset semi-continuous field analyzer at both sites. The semi-empirical EC tracer method was used to derive primary organic carbon (POC) and secondary organic carbon (SOC). Diurnal variations of primary and secondary carbons were observed at T1 and T2, which resulted from boundary layer inversion and impacted by local traffic patterns. The majority of organic carbons at T1 and T2 were secondary. The SOC% (SOC%=SOC/TC*100%) at T1 ranged from 1.2 - 100% with an average of 80.7 ± 14.4%. The SOC% at T2 ranged from 12.8 - 100% with an average of 80.1 ± 14.0%. The average EC to PM2.5 percentage (ECPM%=EC/PM2.5*100%)) and OCPM% were 6.0 % and 20.0% over the whole sampling time. The POC to PM percentage (POCPM%) and SOCPM% were 3.7% and 16.3%, respectively. The maximum ECPM% was 21.2%, and the maximum OCPM% was 57.2%. The maximum POCPM% was 12.9%, and the maximum SOC% was 49.7%. The SOC and POC during T1 to T2 transfer favourable meteorological conditions showed similar characteristics, which indicated that transport between the two supersites took place. Strong correlations between EC and carbon monoxide (CO) and odd nitrogens (NO and NOx) were observed at T1. This indicated that EC had proximate sources such as local traffic emissions. The EC/CO ratio derived by linear regression analysis when parameters are in μgC/m3 and μg/m3, respectively, was 0.0045. A strong correlation was also seen between OC and SOC vs. the sum of oxidants such as O3 and NO2 or O3, NO2 and SO2, suggesting the secondary nature of carbons observed at T1.

  14. Primary and secondary organic carbon downwind of Mexico City

    NASA Astrophysics Data System (ADS)

    Yu, X.-Y.; Cary, R. A.; Laulainen, N. S.

    2009-09-01

    In order to study particulate matter transport and transformation in the Megacity environment, fine particulate carbon was measured simultaneously at two supersites, suburban T1 and rural T2, downwind of Mexico City during the MILAGRO field campaign in March 2006. Organic carbon (OC), element carbon (EC), and total carbon (TC=OC+EC) were determined in near real-time using a Sunset semi-continuous OCEC field analyzer. The semi-empirical EC tracer method was used to derive primary organic carbon (POC) and secondary organic carbon (SOC). Diurnal variations of primary and secondary carbon were observed at T1 and T2, which resulted from boundary layer inversion and impacted by local traffic patterns. The majority of organic carbon particles at T1 and T2 were secondary. The SOCTC% (SOC%=SOC/TC×100%) at T1 ranged from 0.5-93.8% with an average of 63.5±17.2%. The SOCTC% at T2 ranged from 9.3-98.1% with an average of 67.4±12.4%. The average EC to PM2.5 percentage (ECPM%=EC/PM2.5×100%) and OCPM% were 6.0% and 20.0% over the whole sampling time at T1. The POC to PM percentage (POCPM%) and SOCPM% were 3.7% and 16.3%, respectively at the same site. The maximum ECPM% was 21.2%, and the maximum OCPM% was 57.2% at T1. The maximum POCPM% was 12.9%, and the maximum SOCPM% was 49.7% at T1. Comparison of SOC and POC at T1 and T2 showed similar characteristics under favorable meteorological conditions, which indicated that transport from T1 towards T2 took place. Strong correlations between EC and carbon monoxide (CO) and odd nitrogen species (NO and NOx) were observed at T1. This indicated that EC had nearby sources, such as local traffic emissions. The EC/CO ratio derived by linear regression analysis, with units of μg C/m3 and μg/m3, respectively, was 0.004 at T1. Correlations were also seen between OC and SOC vs. the sum of oxidants, such as O3 and NO2, suggesting the secondary nature of carbons observed at T1.

  15. Primary and secondary organic carbon downwind of Mexico City

    NASA Astrophysics Data System (ADS)

    Yu, X.-Y.; Cary, R. A.; Laulainen, N. S.

    2009-01-01

    In order to study particulate matter transport and transformation in the Megacity environment, fine particulate carbons were measured simultaneously at two supersites, suburban T1 and rural T2, downwind of Mexico City during the MILAGRO field campaign in March 2006. Organic carbon (OC), element carbon (EC), and total carbon (TC=OC+EC) were determined in near real-time using a Sunset semi-continuous OC/EC field analyzer. The semi-empirical EC tracer method was used to derive primary organic carbon (POC) and secondary organic carbon (SOC). Diurnal variations of primary and secondary carbons were observed at T1 and T2, which resulted from boundary layer inversion and impacted by local traffic patterns. The majority of organic carbon particles at T1 and T2 were secondary. The SOC% (SOC%=SOC/TC×100%) at T1 ranged from 1.2-100% with an average of 80.7±14.4%. The SOC% at T2 ranged from 12.8-100% with an average of 80.1±14.0%. The average EC to PM2.5 percentage (ECPM%=EC/PM2.5×100%) and OCPM% were 6.0% and 20.0% over the whole sampling time at T1. The POC to PM percentage (POCPM%) and SOCPM% were 3.7% and 16.3%, respectively at the same site. The maximum ECPM% was 21.2%, and the maximum OCPM% was 57.2% at T1. The maximum POCPM% was 12.9%, and the maximum SOCPM% was 49.7% at the suburban site. Comparison of SOC and POC at T1 and T2 showed similar characteristics under favorable meteorological conditions, which indicated that transport between the two supersites took place. Strong correlations between EC and carbon monoxide (CO) and odd nitrogen species (NO and NOx) were observed at T1. This indicated that EC had nearby sources, such as local traffic emissions. The EC/CO ratio derived by linear regression analysis, when parameters in μg C/m3 and μg/m3, respectively, was 0.0045 at T1. Correlations were also seen between OC and SOC vs. the sum of oxidants, such as O3 and NO2, suggesting the secondary nature of carbons observed at T1.

  16. Using Pyrolysis Molecular Beam Mass Spectrometry to Characterize Soil Organic Carbon in Native Prairie Soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The objective of this study was to characterize soil organic carbon (SOC) with pyrolysis molecular beam mass spectrometry (py-MBMS) and then to determine correlations between the mass spectra and associated soil characterization data. Both soil carbon chemistry and the organic forms in which SOC is...

  17. Determination of Water Soluble Organic Carbon Collected ~1 km above the Earth's Surface during a Mid-Atlantic Air Quality Episode and Comparison to Aerosol Optical Properties

    NASA Astrophysics Data System (ADS)

    Brent, L. C.; He, H.; Arkinson, H. L.; Stehr, J. W.; Ring, A.; Marufu, L.; Reiner, J.; Sander, L. C.; Dickerson, R. R.

    2014-12-01

    Routine, light aircraft air-monitoring conducted in MD provides insight into atmospheric photochemical processing as a function of altitude in the boundary layer and lower free troposphere. We present correlations between the optical properties and chemical composition of aerosols at ~1 km altitude over Maryland. Data were collected during the peak smog day and a dissipation day during an air quality episode studied in DISCOVER-AQ, July 2011. Post flight filter sample analysis shows a positive trend between measurable carboxylate concentrations and particle size with a recirculating, aged, urban air mass influenced with southeasterly marine winds (peak day). A westerly influx of air from the Ohio River Valley on the dissipation day was depleted in carboxylates compared with samples collected over the same location two days prior. These samples contained quantifiable concentrations of cis-pinonic acid, a reaction product of pinene after ozonation and photochemical oxidation. New techniques were developed to improve airborne data collection and analysis of water soluble organic acids (WSOA), a frequently dominant fraction of particulate matter (PM). An ion chromatographic mass spectrometric method was developed using NIST Standard Referencing Material 1649b, Urban Dust, as a surrogate material to achieve separation and resolution of at least 34 organic acids. Analysis of aircraft filter samples resulted in detection of 16 organic acids of which 12 were quantified. Eight inorganic species were also quantified. Aged, re-circulated metropolitan air showed a greater number of dicarboxylic acids than new transport air from the west and may provide a useful test of SOA formation theory.

  18. Assessment of methods for organic and inorganic carbon quantification in carbonate-containing Mediterranean soils

    NASA Astrophysics Data System (ADS)

    Apesteguia, Marcos; Virto, Iñigo; Plante, Alain

    2014-05-01

    Quantification of soil organic matter (SOM) stocks and fluxes continues to be an important endeavor in assessments of soil quality, and more broadly in assessments of ecosystem functioning. The quantification of SOM in alkaline, carbonate-containing soils, such as those found in Mediterranean areas, is complicated by the need to differentiate between organic carbon (OC) and inorganic carbon (IC), which continues to present methodological challenges. Acidification is frequently used to eliminate carbonates prior to soil OC quantification, but when performed in the liquid phase, can promote the dissolution and loss of a portion of the OC. Acid fumigation (AF) is increasingly preferred for carbonate removal, but its effectiveness is difficult to assess using conventional elemental and isotopic analyses. In addition, the potential effects of AF on SOM are not well characterized. The objective of the current study was to apply a multi-method approach to determine the efficacy of carbonate removal by AF and its effects on the residual SOM. We selected a set of 24 surface agricultural soils representing a large range of textures, SOM contents and presumed carbonate contents. For each soil, OC was determined using wet combustion (Walkley-Black) and IC was determined using the calcimeter method. Samples were then subjected to elemental (total C) and isotopic (δ13C) analyses by dry combustion using a Costech autoanalyzer coupled to a Thermo Finnigan Delta Plus isotope ratio mass spectrometer (IRMS) before and after AF. IC was equated to total C determined after fumigation, and OC was estimated as the different in total C before and after AF. Samples were also subjected to ramped oxidation using a Netzsch STA109 PC Luxx thermal analyzer coupled to a LICOR 820A infrared gas analyzer (IRGA). Quantification of OC was performed using evolved gas analysis of CO2 (CO2-EGA) in the exothermic region 200-500° C associated with organic matter combustion. IC was quantified by CO2-EGA

  19. High rates of organic carbon burial in fjord sediments globally

    NASA Astrophysics Data System (ADS)

    Smith, Richard W.; Bianchi, Thomas S.; Allison, Mead; Savage, Candida; Galy, Valier

    2015-06-01

    The deposition and long-term burial of organic carbon in marine sediments has played a key role in controlling atmospheric O2 and CO2 concentrations over the past 500 million years. Marine carbon burial represents the dominant natural mechanism of long-term organic carbon sequestration. Fjords--deep, glacially carved estuaries at high latitudes--have been hypothesized to be hotspots of organic carbon burial, because they receive high rates of organic material fluxes from the watershed. Here we compile organic carbon concentrations from 573 fjord surface sediment samples and 124 sediment cores from nearly all fjord systems globally. We use sediment organic carbon content and sediment delivery rates to calculate rates of organic carbon burial in fjord systems across the globe. We estimate that about 18 Mt of organic carbon are buried in fjord sediments each year, equivalent to 11% of annual marine carbon burial globally. Per unit area, fjord organic carbon burial rates are one hundred times as large as the global ocean average, and fjord sediments contain twice as much organic carbon as biogenous sediments underlying the upwelling regions of the ocean. We conclude that fjords may play an important role in climate regulation on glacial-interglacial timescales.

  20. Algae metabolism and organic carbon in sediments determining arsenic mobilisation in ground- and surface water. A field study in Doñana National Park, Spain.

    PubMed

    Kohfahl, Claus; Navarro, Daniel Sánchez-Rodas; Mendoza, Jorge Armando; Vadillo, Iñaki; Giménez-Forcada, Elena

    2016-02-15

    A study has been performed to explore the origin, spatiotemporal behaviour and mobilisation mechanism of the elevated arsenic (As) concentrations found in ground water and drinking ponds of the Doñana National Park, Southern Spain. At a larger scale, 13 piezometers and surface water samples of about 50 artificial drinking ponds and freshwater lagoons throughout the National Park were collected and analysed for major ions, metals and trace elements. At a smaller scale, 5 locations were equipped with piezometers and groundwater was sampled up to 4 times for ambient parameters, major ions, metals, trace elements and iron (Fe) speciation. As was analysed for inorganic and organic speciation. Undisturbed sediment samples were analysed for physical parameters, mineralogy, geochemistry as well as As species. Sediment analyses yielded total As between 0.1 and 18 mg/kg and are not correlated with As concentration in water. Results of the surface- and groundwater sampling revealed elevated concentration of As up to 302 μg/L within a restricted area of the National Park. Results of groundwater sampling reveals strong correlation of As with Fe(2+) pointing to As mobilisation due to reductive dissolution of hydroferric oxides (HFO) in areas of locally elevated amounts of organic matter within the sediments. High As concentrations in surface water ponds are correlated with elevated alkalinity and pH attributed to algae metabolism, leading to As desorption from HFO. The algae metabolism is responsible for the presence of methylated arsenic species in surface water, in contrast to ground water in which only inorganic As species was found. Temporal variations in surface water and groundwater are also related to changes in pH and alkalinity as a result of enhanced algae metabolism in surface water or related to changes in the redox level in the case of groundwater. PMID:26706760

  1. Soil Organic Carbon Change Monitored Over Large Areas

    SciTech Connect

    Brown, David J.; Hunt, E. Raymond; Izaurralde, Roberto C.; Paustian, Keith H.; Rice, Charles W.; Schumaker, Bonny L.; West, Tristram O.

    2010-11-23

    Soils account for the largest fraction of terrestrial carbon (C) and thus are critically important in determining global cycle dynamics. In North America, conversion of native prairies to agriculture over the past 150 years released 30- 50% of soil organic carbon (SOC) stores [Mann, 1986]. Improved agricultural practices could recover much of this SOC, storing it in biomass and soil and thereby sequestering billions of tons of atmospheric carbon dioxide (CO2). These practices involve increasing C inputs to soil (e.g., through crop rotation, higher biomass crops, and perennial crops) and decreasing losses (e.g., through reduced tillage intensity) [Janzen et al., 1998; Lal et al., 2003; Smith et al., 2007].

  2. Carbon- and Nitrogen-Based Organic Frameworks.

    PubMed

    Sakaushi, Ken; Antonietti, Markus

    2015-06-16

    This Account provides an overview of organic, covalent, porous frameworks and solid-state materials mainly composed of the elements carbon and nitrogen. The structures under consideration are rather diverse and cover a wide spectrum. This Account will summarize current works on the synthetic concepts leading toward those systems and cover the application side where emphasis is set on the exploration of those systems as candidates for unusual high-performance catalysis, electrocatalysis, electrochemical energy storage, and artificial photosynthesis. These issues are motivated by the new global energy cycles and the fact that sustainable technologies should not be based on rare and expensive resources. We therefore present the strategic design of functionality in cost-effective, affordable artificial materials starting from a spectrum of simple synthetic options to end up with carbon- and nitrogen-based porous frameworks. Following the synthetic strategies, we demonstrate how the electronic structure of polymeric frameworks can be tuned and how this can modify property profiles in a very unexpected fashion. Covalent triazine-based frameworks (CTFs), for instance, showed both enormously high energy and high power density in lithium and sodium battery systems. Other C,N-based organic frameworks, such as triazine-based graphitic carbon nitride, are suggested to show promising band gaps for many (photo)electrochemical reactions. Nitrogen-rich carbonaceous frameworks, which are developed from C,N-based organic framework strategies, are highlighted in order to address their promising electrocatalytic properties, such as in the hydrogen evolution reaction, oxygen reduction reaction (ORR), and oxygen evolution reaction (OER). With careful design, those materials can be multifunctional catalysts, such as a bifunctional ORR/OER electrocatalyst. Although the majority of new C,N-based materials are still not competitive with the best (usually nonsustainable candidates) for each

  3. Storage of Organic and Inorganic Carbon in Human Settlements

    NASA Astrophysics Data System (ADS)

    Churkina, G.

    2009-12-01

    It has been shown that urban areas have carbon density comparable with tropical forest. Carbon density of urban areas may be even higher, because the density of organic carbon only was taking into account. Human settlements store carbon in two forms such as organic and inorganic. Carbon is stored in organic form in living biomass such as trees, grasses or in artifacts derived from biomass such as wooden furniture, building structures, paper, clothes and shoes made from natural materials. Inorganic carbon or fossil carbon, meanwhile, is primarily stored in objects fabricated by people like concrete, plastic, asphalt, and bricks. The key difference between organic and inorganic forms of carbon is how they return to the gaseous state. Organic carbon can be returned to the atmosphere without applying additional artificial energy through decomposition of organic matter, whereas energy input such as burning is needed to release inorganic carbon. In this study I compare inorganic with organic carbon storage, discuss their carbon residence time, decomposition rates, and possible implications for carbon emissions.

  4. OCoc- from Ocean Colour to Organic Carbon

    NASA Astrophysics Data System (ADS)

    Heim, B.; Overduin, P. P.; Schirrmeister, L.; Lantuit, H.; Doerffer, R.

    2009-12-01

    Enhanced permafrost warming and increased arctic river discharges have heightened concern about the input of terrigenous matter into Arctic coastal waters. The ‘OCoc-from Ocean Colour to Organic Carbon’ project (IPY-project 1176), funded by the German Research Foundation (DFG), is an Ocean Colour study joined with the Arctic Coastal Dynamics ACD network and Arctic Circum-polar Coastal Observatory Network ACCO-Net (IPY-project 90). OCoc uses Ocean Colour satellite data for synoptical monitoring of organic matter fluxes from fluvial and coastal sources. Initial results from German-Russian expeditions at the southeastern Laptev Sea Coast (Arctic Siberia, Russia) in August 2008 and August 2009 are presented. Large parts of this coastal zone are characterized by highly erosive organic-rich material. Ocean Colour MERIS Reduced Resolution (RR)-LIB data of the have been processed towards optical aquatic parameters using Beam-Visat4.2 and the MERIS case2 regional processor for coastal application (C2R). Calculated aquatic parameters are absorption and backscattering coefficients, apparent optical properties such as the first attenuation depth (‘Z90’) and calculated concentrations of chlorophyll, total suspended matter and coloured dissolved organic matter absorption from the water leaving reflectances. Initial comparisons with expedition data (Secchi depths, cDOM) show that the MERIS-C2R optical parameters ’total absorption’ and the first attenuation depth, ’Z90’, seem adequately to represent true conditions. High attenuation values in the spectral blue wavelength range may serve as tracer for the organic-rich terrigenous input. The synoptic information of Ocean Colour products will provide valuable spatial and dynamical information on the Organic Carbon and sediment fluxes from the Siberian permafrost coast.

  5. Black Carbon in Sedimentary Organic Carbon in the Northeast Pacific using the Benzene Polycarboxylic Acid Method

    NASA Astrophysics Data System (ADS)

    Coppola, A. I.; Ziolkowski, L. A.; Druffel, E. R.

    2010-12-01

    Black carbon (BC) in the Northeast Pacific ultrafiltered dissolved organic matter (UDOM) was found to be surprisingly old with a 14C age of 18,000 +/-3,000 14C years (Ziolkowski and Druffel, 2010) using the Benzene Polycarboxylic Acid (BPCA) method, while BC in sedimentary organic carbon (SOC) was found to be 2,400-12,900 14C years older than non-BC SOC (Masiello and Druffel, 1998) with a different method. Using the dichromate-sulfuric acid oxidation method (Wolbach and Anders, 1989), Masiello and Druffel (1998) estimated that 12-31% of SOC in the Northeast Pacific and the Southern Ocean surface sediments was black carbon (BC). However, the dichromate-sulfuric acid oxidation may over-estimate the concentration of BC, because this method is more biased toward modern (char) material (Currie et al., 2002). Alternatively, the BPCA method isolates aromatic components of BC as benzene rings substituted with carboxylic acid groups, and provides structural information about the BC. Recent modifications to the BPCA method by Ziolkowski and Druffel (2009) involve few biases in quantifying BC in the continuum between char and soot in UDOM. Here we use the BPCA method to determine the concentrations and 14C values of BC in sediments from three sites in the Northeast Pacific Ocean. Constraining the difference between non-BC SOC and BC-SOC using the BPCA method allows for a more precise estimate of how much BC is present in the sediments and its 14C age. Presumably, the intermediate reservoir of BC is oceanic dissolved organic carbon (DOC) and is, in part, responsible for DOC’s great 14C age. These results can be utilized to better constrain the oceanic carbon budget as a possible sink of BC. References: Currie, L. A., Benner Jr., B. A., Kessler, J.D., et al (2002), A critical evaluation of interlaboratory data on total, elemental, and isotopic carbon in the carbonaceous particle reference material, nist srm 1649a, J. Res. Natl. Inst. Stand. Technol., 107, 279-298. Masiello, C

  6. Fate of Organic Micropollutants during Hydrothermal Carbonization

    NASA Astrophysics Data System (ADS)

    Weiner, B.; Baskyr, I.; Pörschmann, J.; Kopinke, F.-D.

    2012-04-01

    The hydrothermal carbonization (HTC) is an exothermic process, in which biomass in an aqueous suspension is transformed into a bituminous coal-like material (hydrochar) at temperatures between 180-250°C and under moderate pressure. With these process conditions, little gas is generated (1-5%), and a fraction of the organic carbon is dissolved in the aqueous phase (10-30%) but the largest part is obtained as solid char. The respective yields and the molecular composition depend on the choice of educts and the process conditions, such as temperature, pH-value, and reaction time. Various biomass-educts have recently been studied, such as waste materials from agriculture, brewer's spent grains, sewage sludge, as well as wood and paper materials. Besides their use for energy generation, the hydrochars have also been investigated as soil amendments. Prior to addition of the chars to soil, these should be free of toxic components that could be released into the environment as harmful organic pollutants. Herein, the potential for the degradation of trace organic pollutants, such as pesticides and pharmaceuticals, under typical HTC conditions will be presented. The degradation of selected organic pollutants with different polarity and hydrophobicity was investigated. Scope and limitations of the degradation potential of the HTC are discussed on examples of micro pollutants such as hormones, residues of pharmaceuticals and personal care products including their metabolites, and pesticides. We will show that the target analytes are partially and in some cases completely degraded. The degree of degradation depends on the HTC process conditions such as reaction temperature and time, the solution pH value, the presence of catalysts or additional reagents. The biotic and abiotic degradation of chlorinated organic compounds, in particular chlorinated aromatics, has been a well-known environmental problem and remains a challenging issue for the development of a HTC process for

  7. Multi-walled carbon nanotubes and metal-organic framework nanocomposites as novel hybrid electrode materials for the determination of nano-molar levels of lead in a lab-on-valve format.

    PubMed

    Wang, Yang; Wu, Yichun; Xie, Jing; Ge, Huali; Hu, Xiaoya

    2013-09-01

    Metal-organic frameworks have been the subject of intense research because of their unique physicochemical properties. The presented study investigates the application of multi-wall carbon nanotubes and metal-organic frameworks (MWCNTs@Cu3(BTC)2) nanoparticles-modified electrode for the determination of trace levels of lead. The nanocomposites were prepared by solvothermal synthesis and characterized in detail. The experimental procedure was carried out by accumulating lead on the electrode surface and subsequently measuring with differential pulse anodic stripping voltammetry in a lab-on-valve format. The main parameters affecting the analytical performance, including the amount of MWCNTs@Cu3(BTC)2 suspension, supporting electrolyte and its pH, stripping mode, and flow rate, have been investigated in detail. Under the optimum conditions, the oxidation peak current displayed a calibration response for lead over a concentration range from 1.0 × 10(-9) to 5.0 × 10(-8) mol L(-1) with a excellent detection limit of 7.9 × 10(-10) mol L(-1). The relative standard deviation of 7 successive scans was 3.10% for 1.0 × 10(-8) mol L(-1) lead. The established method showed a great improvement in sensitivity and sample throughput for lead analysis. PMID:23853779

  8. Dissolved organic carbon in rainwater: Glassware decontamination and sample preservation and volatile organic carbon

    NASA Astrophysics Data System (ADS)

    Campos, M. L. A. M.; Nogueira, R. F. P.; Dametto, P. R.; Francisco, J. G.; Coelho, C. H.

    The efficiency of different methods for the decontamination of glassware used for the analysis of dissolved organic carbon (DOC) was tested using reported procedures as well as new ones proposed in this work. A Fenton solution bath (1.0 mmol L -1 Fe 2+ and 100 mmol L -1 H 2O 2) for 1 h or for 30 min employing UV irradiation showed to combine simplicity, low cost and high efficiency. Using the optimized cleaning procedure, the DOC for stored UV-irradiated ultra-pure water reached concentrations below the limit of detection (0.19 μmol C L -1). Filtered (0.7 μm) rain samples maintained the DOC integrity for at least 7 days when stored at 4 °C. The volatile organic carbon (VOC) fraction in the rain samples collected at two sites in São Paulo state (Brazil) ranged from 0% to 56% of their total DOC content. Although these high-VOC concentrations may be derived from the large use of ethanol fuel in Brazil, our results showed that when using the high-temperature catalytic oxidation technique, it is essential to measure DOC rather than non-purgeble organic carbon to estimate organic carbon, since rainwater composition can be quite variable, both geographically and temporally.

  9. Organic carbon-14 in the Amazon River system

    SciTech Connect

    Hedges, J.I.; Ertel, J.R.; Quay, P.D.; Grootes, P.M.; Richey, J.E.; Devol, A.H.; Farwell, G.W.; Schmidt, F.W.; Salati, E.

    1986-03-07

    Coarse and fine suspended particulate organic materials and dissolved humic and fulvic acids transported by the Amazon River all contain bomb-produced carbon-14, indicating relatively rapid turnover of the parent carbon pools. However, the carbon-14 contents of these coexisting carbon forms are measurably different and may reflect varying degrees of retention by soils in the drainage basin. 20 references, 1 table.

  10. Determination of total organic emissions from hazardous waste combustors.

    PubMed

    Johnson, L D

    1996-01-01

    U.S. Environmental Protection Agency risk assessment guidance currently under development for evaluation of permitting information from hazardous waste combustors requires a quantity referred to as "total organic carbon". The risk guidance does not define this term precisely, nor does it explain how it should be determined. This paper discusses basic principles of sampling and analysis of stack emissions for "total organics", best currently available technology, and the status of two ongoing projects designed to provide guidance and to improve analysis procedures. Determination of total organics from stack emissions is much more complicated than might be expected, and more published guidance is badly needed. The best scheme available for analysis of stack emissions for total organics to be used in material balance style "bookkeeping" includes determination of organics content in three boiling point ranges:  <100 °C, 100 °C-300 °C, and >300 °C. Total organic carbon is not a useful quantity, since it includes soot, polymeric material, and other nonextractable organic materials. Total organics has been found to be an imperfect but less misleading term. Various calculations can be made and conclusions can be drawn on the basis of the contents of the individual boiling point ranges, as determined by the recommended methodology. The analysis strategy is complicated and difficult, and it contains limitations and compromises. It does not, however, require exotic analysis instrumentation, nor is it very expensive. Each of these facets of the methodology is discussed in this paper, and a status report is provided on development of a guidance document and a research project intended to produce improved methods. PMID:21619231

  11. A method for smoke marker measurements and its potential application for determining the contribution of biomass burning from wildfires and prescribed fires to ambient PM2.5 organic carbon

    NASA Astrophysics Data System (ADS)

    Sullivan, A. P.; Holden, A. S.; Patterson, L. A.; McMeeking, G. R.; Kreidenweis, S. M.; Malm, W. C.; Hao, W. M.; Wold, C. E.; Collett, J. L.

    2008-11-01

    Biomass burning is an important source of particulate organic carbon (OC) in the atmosphere. Quantifying this contribution in time and space requires a means of routinely apportioning contributions of smoke from biomass burning to OC. Smoke marker (for example, levoglucosan) measurements provide the most common approach for making this determination. A lack of source profiles for wildfires and prescribed fires and the expense and complexity of traditional smoke marker measurement methods have thus far limited routine estimates of these contributions to ambient aerosol concentrations and regional haze. We report here on the collection of source profiles for combustion of numerous wildland fuels and on the development of an inexpensive and robust technique for routine smoke marker measurements. Hi-Volume filter source samples were collected during two studies at the Fire Science Laboratory in Missoula, MT in 2006 and 2007. Levoglucosan (and other carbohydrates) were measured in these samples using high-performance anion-exchange chromatography with pulsed amperometric detection. Results of this analysis along with water-soluble potassium, OC, and elemental carbon are presented. The results show that emissions of levoglucosan are fairly correlated with OC with an average ratio of 0.031 μg C/μg C. Further, there was a definite pattern that emerged based on fuel component burned with the typical levoglucosan/OC ratio of branches > straw > needles > leaves. Additionally, this carbohydrate measurement method appears to provide fingerprint information about the type of fuel burned that could help constrain profiles chosen for aerosol source apportionment and lead to a better determination of source contributions from biomass burning.

  12. Munsell color value as related to organic carbon in Devonian shale of Appalachian basin

    USGS Publications Warehouse

    Hosterman, J.W.; Whitlow, S.I.

    1981-01-01

    Comparison of Munsell color value with organic carbon content of 880 samples from 50 drill holes in Appalachian basin shows that a power curve is the best fit for the data. A color value below 3 to 3.5 indicates the presence of organic carbon but is meaningless in determining the organic carbon content because a large increase in amount of organic carbon causes only a minor decrease in color value. Above 4, the color value is one of the factors that can be used in calculating the organic content. For samples containing equal amounts of organic carbon, calcareous shale containing more than 5% calcite is darker than shale containing less than 5% calcite.-Authors

  13. A method for quantifying bioavailable organic carbon in aquifer sediments

    USGS Publications Warehouse

    Rectanus, H.V.; Widdowson, M.; Novak, J.; Chapelle, F.

    2005-01-01

    The fact that naturally occurring microorganisms can biodegrade PCE and TCE allows the use of monitored natural attenuation (MNA) as a remediation strategy at chlorinated solvent-contaminated sites. Research at numerous chlorinated solvent sites indicates an active dechlorinating microbial population coupled with an ample supply of organic carbon are conditions needed to sustain reductive dechlorination. A series of extraction experiments was used to compare the ability of the different extractants to remove organic carbon from aquifer sediments. The different extractants included pyrophosphate, sodium hydroxide, and polished water. Pyrophosphate served as a mild extractant that minimally alters the organic structure of the extracted material. Three concentrations (0.1, 0.5, and 1%) of pyrophosphate extracted 18.8, 24.9, and 30.8% of sediment organic carbon, respectively. Under alkali conditions (0.5 N NaOH), which provided the harshest extractant, 30.7% of the sediment organic carbon was recovered. Amorphous organic carbon, measured by potassium persulfate oxidization, consisted of 44.6% of the sediment organic carbon and served as a baseline control for maximum carbon removal. Conversely, highly purified water provided a minimal extraction control and extracted 5.7% of the sediment organic carbon. The removal of organic carbon was quantified by aqueous TOC in the extract and residual sediment organic carbon content. Characterization of the organic carbon extracts by compositional analysis prior and after exposure to the mixed culture might indicate the type organic carbon and functional groups used and/or generated by the organisms. This is an abstract of a paper presented at the 8th International In Situ and On-Site Bioremediation Symposium (Baltimore, MD 6/6-9/2005).

  14. SAMPLING ARTIFACTS IN MEASUREMENT OF ELEMENTAL AND ORGANIC CARBON: LOW VOLUME SAMPLING IN INDOOR AND OUTDOOR ENVIRONMENTS

    EPA Science Inventory

    Experiments were completed to determine the extent of artifacts from sampling elemental carbon (EC) and organic carbon (OC) under sample conditions consistent with personal sampling. Two different types of experiments were completed; the first examined possible artifacts from oil...

  15. Selective stabilization of aliphatic organic carbon by iron oxide

    PubMed Central

    Adhikari, Dinesh; Yang, Yu

    2015-01-01

    Stabilization of organic matter in soil is important for natural ecosystem to sequestrate carbon and mitigate greenhouse gas emission. It is largely unknown what factors govern the preservation of organic carbon in soil, casting shadow on predicting the response of soil to climate change. Iron oxide was suggested as an important mineral preserving soil organic carbon. However, ferric minerals are subject to reduction, potentially releasing iron and decreasing the stability of iron-bound organic carbon. Information about the stability of iron-bound organic carbon in the redox reaction is limited. Herein, we investigated the sorptive interactions of organic matter with hematite and reductive release of hematite-bound organic matter. Impacts of organic matter composition and conformation on its sorption by hematite and release during the reduction reaction were analyzed. We found that hematite-bound aliphatic carbon was more resistant to reduction release, although hematite preferred to sorb more aromatic carbon. Resistance to reductive release represents a new mechanism that aliphatic soil organic matter was stabilized by association with iron oxide. Selective stabilization of aliphatic over aromatic carbon can greatly contribute to the widely observed accumulation of aliphatic carbon in soil, which cannot be explained by sorptive interactions between minerals and organic matter. PMID:26061259

  16. An Assessment of The Contribution of Organic Carbon of Terrigenous Origin To The Total Organic Carbon In Sediments In Scottish Coastal Waters (sea Lochs and Shelf Depressions)

    NASA Astrophysics Data System (ADS)

    Loh, P. S.; Reeves, A. D.; Overnell, J.; Harvey, M.; Miller, A.

    Sedimentary organic carbon is of global importance because it represents a significant sink of fixed carbon, which is being lost from the biosphere through eventual burial. In the process some carbon is remineralized which fuels marine biogeochemical cycles and returns most of the bound nutrients to the water column. In addition it may bind anthropogenic contaminants, such as heavy metals and PCBs which are removed from the water column. Sea lochs are representative of low energy hydrographic regimes and act as traps for sediment, which generally accumulates at high rat es. The sediments are associated with enhanced levels of terrigenous input, and are rich in organic matter. Further out to sea towards the shelf break, sedimentation rates decrease and the contribution of carbon of marine origin to the total decreases. It is generally considered that organic carbon of marine origin is readily degradable and that organic carbon of terrestrial origin is refractory and eventually becomes integrated into permanent sediment deposits. Thus terrigenous particulate organic carbon would be transported across the shelf and deposited on the shelf slope. Recent experiments have shown however, that on a transect from the head of Loch Etive (West Coast of Scotland) to the sea, it is the input of particulate terrigenous organic carbon that seems to determine the oxygen uptake rates. Work presented in this paper is being undertaken in association with the Centre for Coastal and Marine Sciences core programme, Restricted Exchange Environments. The wider study involves measuring processes such as oxygen uptake rates, sulphate reduction rates and total sediment carbon contents. The aims of the research presented here is to assess the contribution of terrigenous organic carbon to total carbon inputs; to assess degradation of organic carbon; to measure lignin content of sediment; to compare sedimentation rates with those outside the loch and to measure sedimentary carbon of marine

  17. Influence of organic carbon on estuarine benthic infauna of the US west coast

    EPA Science Inventory

    Total organic carbon (TOC) is often used as an indicator of eutrophication in estuarine environments. However, the determination of biologically relevant sediment TOC criteria to indicate estuarine condition is complicated by the relationship between TOC and grain size. Both va...

  18. Influence of organic carbon on estuarine benthic infauna of the US west coast - March 3, 2011

    EPA Science Inventory

    Total organic carbon (TOC) is often used as an indicator of eutrophication in estuarine environments. However, the determination of biologically relevant sediment TOC criteria to indicate estuarine condition is complicated by the relationship between TOC and grain size. Both va...

  19. Influence of sediment organic carbon on estuarine benthic species of the US West Coast

    EPA Science Inventory

    Total organic carbon (TOC) is often used as an indicator of nutrient enrichment in estuarine environments. However, the determination of biologically relevant TOC criteria to indicate sediment quality is complicated by the relationship between TOC and grain size. Both variables...

  20. Comparing the methods for determination of carbon in soil

    NASA Astrophysics Data System (ADS)

    Bidló, A.; Szżcs, P.; Horváth, A.; Kámán, O.; Németh, E.; Juhász, P.

    2012-04-01

    The global climate change raised the question of carbon sequestration of forests. Forests are important natural carbon sequesters in the temperate zone. It can be ascertained, that a significant part of carbon (often more than half of it), can be found in the soil. The greater amount of carbon can be found in the organic substance of soil (humus). There are several methods for determination of carbon in soil. The most popular method is determination by dry-burning, which means that the samples are exposed to high temperature and the amount of carbon content of CO2 becomes observable with the help of thermal conductivity detector or infrared spectroscopy. The advantage of this system is that burning and carbon content determination happens in a reproducible way if the conditions are satisfactory. However, this method is limited, because e. g. in Hungary the soil contains too much lime (often above 50%) and during the burning CO2 evolves from decomposition of minerals. The previous hydrochloric destruction of carbonate is not usable for lime content during examination. In the case of soils with high lime content the application of wet oxidation by potassium dichromate for organic matter determination is correct. During our investigation we made a comparison between the results of dry and three different wet burning, in the same way we did with organic matter determination in parallel with the determination of 320 soil samples. Between the results of wet burning we detected a decided difference. The Tyurin-type humus (Benediktas 2006, Tóth and Szabó 2003) determination (which is widely applied in Eastern Europe and it is a gas burning destruction method) showed high dispersion. The other destruction method showed favourable results, this method is applied on water bath, and is corresponding to the Hungarian standard. The correlation coefficient was between 0,87 és 0,98 amongst three analytical methods. We made a comparison between results of wet and dry burning

  1. Elevated dissolved organic carbon biodegradability from thawing and collapsing permafrost

    NASA Astrophysics Data System (ADS)

    Abbott, Benjamin W.; Larouche, Julia R.; Jones, Jeremy B.; Bowden, William B.; Balser, Andrew W.

    2014-10-01

    As high latitudes warm, a portion of the large organic carbon pool stored in permafrost will become available for transport to aquatic ecosystems as dissolved organic carbon (DOC). If permafrost DOC is biodegradable, much will be mineralized to the atmosphere in freshwater systems before reaching the ocean, accelerating carbon transfer from permafrost to the atmosphere, whereas if recalcitrant, it will reach marine ecosystems where it may persist over long time periods. We measured biodegradable DOC (BDOC) in water flowing from collapsing permafrost (thermokarst) on the North Slope of Alaska and tested the role of DOC chemical composition and nutrient concentration in determining biodegradability. DOC from collapsing permafrost was some of the most biodegradable reported in natural systems. However, elevated BDOC only persisted during active permafrost degradation, with a return to predisturbance levels once thermokarst features stabilized. Biodegradability was correlated with background nutrient concentration, but nutrient addition did not increase overall BDOC, suggesting that chemical composition may be a more important control on DOC processing. Despite its high biodegradability, permafrost DOC showed evidence of substantial previous microbial processing, and we present four hypotheses explaining this incongruity. Because thermokarst features form preferentially on river banks and lake shores and can remain active for decades, thermokarst may be the dominant short-term mechanism delivering sediment, nutrients, and biodegradable organic matter to aquatic systems as the Arctic warms.

  2. Soil Organic Carbon Degradation, Barrow, 2013-2014

    DOE Data Explorer

    Gu, Baohua; Yang, Ziming

    2015-03-30

    This dataset provides information about soil organic carbon decomposition in Barrow soil incubation studies. The soil cores were collected from low-center polygon (Area A) and were incubated in the laboratory at different temperatures for up to 60 days. Transformations of soil organic carbon were characterized by UV and FT-IR, and small organic acids in water-soluble carbons were quantified by ion chromatography during the incubation

  3. Hidden cycle of dissolved organic carbon in the deep ocean

    PubMed Central

    Follett, Christopher L.; Repeta, Daniel J.; Rothman, Daniel H.; Xu, Li; Santinelli, Chiara

    2014-01-01

    Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ13C and age via Δ14C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle. PMID:25385632

  4. Aged Riverine Particulate Organic Carbon in Four UK Catchments

    NASA Astrophysics Data System (ADS)

    Adams, Jessica; Tipping, Edward; Bryant, Charlotte; Helliwell, Rachel; Toberman, Hannah; Quinton, John

    2016-04-01

    The riverine transport of particulate organic matter (POM) is a significant flux in the carbon cycle, and affects macronutrients and contaminants. We used radiocarbon to characterise POM at 9 riverine sites of four UK catchments (Avon, Conwy, Dee, Ribble) over a one-year period. High-discharge samples were collected on three or four occasions at each site. Suspended particulate matter (SPM) was obtained by centrifugation, and the samples were analysed for carbon isotopes. Concentrations of SPM and SPM organic carbon (OC) contents were also determined, and were found to have a significant negative correlation. For the 7 rivers draining predominantly rural catchments, PO14C values, expressed as percent modern carbon absolute (pMC), varied little among samplings at each site, and there was no significant difference in the average values among the sites. The overall average PO14C value for the 7 sites of 91.2 pMC corresponded to an average age of 680 14C years, but this value arises from the mixing of differently-aged components, and therefore significant amounts of organic matter older than the average value are present in the samples. Although topsoil erosion is probably the major source of the riverine POM, the average PO14C value is appreciably lower than topsoil values (which are typically 100 pMC). This is most likely explained by inputs of older subsoil OC from bank erosion, or the preferential loss of high-14C topsoil organic matter by mineralisation during riverine transport. The significantly lower average PO14C of samples from the River Calder (76.6 pMC), can be ascribed to components containing little or no radiocarbon, derived either from industrial sources or historical coal mining, and this effect is also seen in the River Ribble, downstream of its confluence with the Calder. At the global scale, the results significantly expand available information for PO14C in rivers draining catchments with low erosion rates.

  5. Aged riverine particulate organic carbon in four UK catchments.

    PubMed

    Adams, Jessica L; Tipping, Edward; Bryant, Charlotte L; Helliwell, Rachel C; Toberman, Hannah; Quinton, John

    2015-12-01

    The riverine transport of particulate organic matter (POM) is a significant flux in the carbon cycle, and affects macronutrients and contaminants. We used radiocarbon to characterise POM at 9 riverine sites of four UK catchments (Avon, Conwy, Dee, Ribble) over a one-year period. High-discharge samples were collected on three or four occasions at each site. Suspended particulate matter (SPM) was obtained by centrifugation, and the samples were analysed for carbon isotopes. Concentrations of SPM and SPM organic carbon (OC) contents were also determined, and were found to have a significant negative correlation. For the 7 rivers draining predominantly rural catchments, PO14C values, expressed as percent modern carbon absolute (pMC), varied little among samplings at each site, and there was no significant difference in the average values among the sites. The overall average PO14C value for the 7 sites of 91.2 pMC corresponded to an average age of 680 14C years, but this value arises from the mixing of differently-aged components, and therefore significant amounts of organic matter older than the average value are present in the samples. Although topsoil erosion is probably the major source of the riverine POM, the average PO14C value is appreciably lower than topsoil values (which are typically 100 pMC). This is most likely explained by inputs of older subsoil OC from bank erosion, or the preferential loss of high-14C topsoil organic matter by mineralisation during riverine transport. The significantly lower average PO14C of samples from the River Calder (76.6 pMC), can be ascribed to components containing little or no radiocarbon, derived either from industrial sources or historical coal mining, and this effect is also seen in the River Ribble, downstream of its confluence with the Calder. At the global scale, the results significantly expand available information for PO14C in rivers draining catchments with low erosion rates. PMID:26254066

  6. Soil organic carbon assessments in cropping systems using isotopic techniques

    NASA Astrophysics Data System (ADS)

    Martín De Dios Herrero, Juan; Cruz Colazo, Juan; Guzman, María Laura; Saenz, Claudio; Sager, Ricardo; Sakadevan, Karuppan

    2016-04-01

    Introduction of improved farming practices are important to address the challenges of agricultural production, food security, climate change and resource use efficiency. The integration of livestock with crops provides many benefits including: (1) resource conservation, (2) ecosystem services, (3) soil quality improvements, and (4) risk reduction through diversification of enterprises. Integrated crop livestock systems (ICLS) with the combination of no-tillage and pastures are useful practices to enhance soil organic carbon (SOC) compared with continuous cropping systems (CCS). In this study, the SOC and its fractions in two cropping systems namely (1) ICLS, and (2) CCS were evaluated in Southern Santa Fe Province in Argentina, and the use of delta carbon-13 technique and soil physical fractionation were evaluated to identify sources of SOC in these systems. Two farms inside the same soil cartographic unit and landscape position in the region were compared. The ICLS farm produces lucerne (Medicago sativa Merrill) and oat (Avena sativa L.) grazed by cattle alternatively with grain summer crops sequence of soybean (Glicine max L.) and corn (Zea mays L.), and the farm under continuous cropping system (CCS) produces soybean and corn in a continuous sequence. The soil in the area is predominantly a Typic Hapludoll. Soil samples from 0-5 and 0-20 cm depths (n=4) after the harvest of grain crops were collected in each system and analyzed for total organic carbon (SOC, 0-2000 μm), particulate organic carbon (POC, 50-100 μm) and mineral organic carbon (MOC, <50 μm). Delta carbon-13 was determined by isotopic ratio mass spectrometry. In addition, a site with natural vegetation (reference site, REF) was also sampled for delta carbon-13 determination. ANOVA and Tukey statistical analysis were carried out for all data. The SOC was higher in ICLS than in CCS at both depths (20.8 vs 17.7 g kg-1 for 0-5 cm and 16.1 vs 12.7 g kg-1 at 0-20 cm, respectively, P<0.05). MOC was

  7. Development of a rapid assimilable organic carbon method for water.

    PubMed

    Lechevallier, M W; Shaw, N E; Kaplan, L A; Bott, T L

    1993-05-01

    A rapid method for measurement of assimilable organic carbon (AOC) is proposed. The time needed to perform the assay is reduced by increasing the incubation temperature and increasing the inoculum density. The ATP luciferin-luciferase method quickly enumerates the test organisms without the need for plate count media or dilution bottles. There was no significant difference between AOC values determined with strain P17 for the ATP and plate count procedures. For strain NOX, the plate count procedure underestimated bacterial levels in some samples. Comparison of AOC values obtained by the Belleville laboratory (by the ATP technique) and the Stroud Water Research Center (by plate counts) showed that values were significantly correlated and not significantly different. The study concludes that the rapid AOC method can quickly determine the bacterial growth potential of water within 2 to 4 days. PMID:16348936

  8. Examining organic carbon transport by the Orinoco River using SeaWiFS imagery

    NASA Astrophysics Data System (ADS)

    López, Ramón; Del Castillo, Carlos E.; Miller, Richard L.; Salisbury, Joseph; Wisser, Dominik

    2012-09-01

    The Orinoco River is the fourth largest in the world in terms of water discharge and organic carbon export to the ocean. River export of organic carbon is a key component of the carbon cycle and the global carbon budget. Here, we examined the seasonal transport of organic carbon by the Orinoco River into the eastern Caribbean using the conservative relationship of colored dissolved organic matter (CDOM) and dissolved organic carbon (DOC) in low salinity coastal waters influenced by river plumes. In situ measurements of CDOM absorption, DOC, and salinity were used to develop an empirical model for DOC concentration at the Orinoco River Plume. Satellite remote sensing reflectances were used with empirical models to determine DOC and Particulate organic carbon (POC) river transport. Our estimates of CDOM and DOC significantly correlated with in situ measurements and were within the expected ranges for the river. Total organic carbon transport by the Orinoco River during the period of 1998 to 2010 was 7.10 ×1012 g C y-1, from 5.29 × 1012 g C y-1 of DOC and 1.81 × 1012 g C y-1 of POC, representing ˜6% increase to previous published estimates. The variability in organic carbon transport responded to the seasonality in river flow more than to changes in organic carbon concentration in the river. Our results corroborate that is possible to estimate organic carbon transport using ocean color data at global scales. This is needed to reduce the uncertainties of land-ocean carbon fluxes.

  9. Method 440.0 Determination of Carbon and Nitrogen in Sediments and Particulatesof Estuarine/Coastal Waters Using Elemental Analysis

    EPA Science Inventory

    Elemental analysis is used to determine particulate carbon (PC) and particulate nitrogen (PN) in estuarine and coastal waters and sediment. The method measures the total carbon and nitrogen irrespective of source (inorganic or organic).

  10. [Organic Carbon and Elemental Carbon in Forest Biomass Burning Smoke].

    PubMed

    Huang, Ke; Liu, Gang; Zhou, Li-min; Li, Jiu-hai; Xu, Hui; Wu, Dan; Hong, Lei; Chen, Hui-yu; Yang, Wei-zong

    2015-06-01

    Ten kinds of trees were selected for preparing dry and wet stick samples. Concentrations of organic carbon (OC), elemental carbon (EC) in particular matter produced by sticks samples in the flaming and smoldering were analyzed through the Thermal Optical Carbon Analyzer (Model 2001A). The results showed that mean values of OC (EF(OC)), EC (EF(EC)), PM (EF(PM)) emission factors were 6.8, 2.1, 16.5 g x kg(-1) in the dry stick flaming smoke, 57.5, 11.1, 130.9 g x kg(-1) in the dry stick smoldering smoke, 13.6, 3.3, 30.5 g x kg(-1) in the wet stick flaming smoke, 57.6, 9.6, 125.6 g x kg(-1) in the wet stick smoldering smoke. Compared to the flaming condition, EF(OC), EF(EC), EF(PM), were much higher in the smoldering condition. In the flaming condition, EF(OC), EF(EC), EF(PM) had positive correlations with the moisture content. The mean values of OC/PM, EC/PM, TC/PM (TC = OC + EC) were 45%, 10%, 55%, and the mass fractions of OC was much higher in smoldering condition than those in flaming condition, but the mass fractions of EC was lower in the smoldering condition. Compared to dry sticks, the smoke of wet sticks combustion had higher mass fractions of OC and lower mass fractions of EC. The mean value of OC/EC was 3.3 (2.5-5.2) in the dry stick flaming smoke, and was 5.2 (4.3-6.3) in the dry stick smoldering smoke, in the wet stick flaming smoke was 4.1 (3.1-5.3), and was 6.2 (4.2-8.4) in the wet stick smoldering smoke. Compared to the flaming condition, the mean value of OC/EC was higher in the smoldering condition, and the mean value of OC/EC was much higher in high moisture content stick combustion smoke. The correlation coefficient between OC and EC was 0.985 in dry stick combustions, and was 0.915 in wet stick combustions. So, based on the flaming and smoldering condition, the correlation between OC and EC was significant in different moisture contents of sticks. PMID:26387300

  11. Possible method for dissolved organic carbon speciation in forest soils

    NASA Astrophysics Data System (ADS)

    Drabek, O.; Tejnecký, V.; Ash, C.; Hubova, P.; Boruvka, L.

    2013-12-01

    Dissolved organic carbon (DOC) is a natural part of dissolved organic matter and it plays an important role in the biogeochemistry of soil processes. Low Molecular Mass Organic Acids (LMMOA) are an essential part of DOC. These acids play a key role in chemical processes that affect the entire soil environment. Knowing the amount of DOC and the speciation of LMMOA is required for realistic equilibrium modelling of soil chemical processes and transport mechanisms. There have been a number of proposed methods for the quantitative analysis of DOC and for speciation of LMMOA. The first aim of this contribution is to introduce and test a modified spectroscopic method for the determination of water-extractable organic carbon (WEOC) from forest soils. In general this method is based on the oxidization of WEOC by chromium-sulphuric acid. The presented method can be used as an economical alternative to the classical, more financially demanding elemental analysis. However, the main aim is to test the reliability of the method for LMMOA speciation. Ion exchange chromatography (IC) with hydroxide elution has proven to be a useful tool for the determination of LMMOA in many different water-based samples. However, the influence of multivalent cations (often present in environmental samples) on IC results has not yet been sufficiently studied. In order to assess the influence of Al, Fe, Mn, Mg and Ca on the amount of LMMOA determined by IC, an extensive set of model solutions was prepared and immediately analysed by means of IC. Moreover, the influence of pH on determined amounts of LMMOA in model solutions and representative soil aqueous extracts was investigated. These experimental results were compared to expected values and also to results provided by the chemical equilibrium model - PHREEQC. Based on the above listed research, some modifications to the common IC method for LMMOA speciation are presented.

  12. Transient Dissolved Organic Carbon Through Soils

    NASA Astrophysics Data System (ADS)

    Mei, Y.; Hornberger, G. M.; Kaplan, L. A.; Newbold, J. D.; Aufdenkampe, A. K.; Tsang, Y.

    2009-12-01

    Dissolved organic carbon (DOC) is an important constituent of soil solution that plays a role in many chemical and biological processes in soils; it is also an important energy source for bacteria in the soil ecosystem. Hydrology has a significant control on the transport and fate of dissolved organic carbon in the soil but mechanisms that affect said transport are not well understood. In particular, dynamic information on DOC transport through forest soils on short time scales (one or two precipitation event) is lacking at present. DOC is a very complex mix of organic compounds. A key to quantifying DOC dynamics is to establish useful approximations for behavior of this complex mixture. Biodegradable dissolved organic carbon (BDOC) is an important part of DOC. It is reported that between 12 and 44% of DOC released from the forest floor can be decomposed in solutions by indigenous microbes. In our study, we considered how DOC, BDOC, and flow interact in soil columns. In-situ soil cores with two different lengths were installed under a mixed deciduous canopy. The effects of artificial rain on DOC and BDOC transport were examined by dripping nano pure water amended with bromide on the top of soil cores and sampling the water collected at the bottom of the cores for DOC and BDOC. We used plug-flow biofilm reactors to measure the BDOC concentration. It is likely that reduced rates of decomposition in dry soils will cause microbial products of DOC to accumulate; hence DOC concentration should be high at the first flush of rain and decline as the event proceeds. The experimental results show the expected pattern, that is, the first samples we collected always had the highest DOC and BDOC concentrations. The concentrations tend to decline through the simulated precipitation event. Application of a second “storm” forty minutes after the cessation of the first application of water resulted in effluent DOC concentration increasing a small amount initially and then

  13. Role of organic soils in the world carbon cycle: problem analysis and research needs

    SciTech Connect

    Armentano, T.V.

    1980-02-01

    In May 1979, The Institute of Ecology held a workshop to determine the role of organic soils in the global carbon cycle and to ascertain their past, present and future significance in world carbon flux. Wetlands ecologists and soil scientists who participated in the workshop examined such topics as Soils as Sources of Atmospheric CO/sub 2/, Organic Soils, Primary Production and Growth of Wetlands Ecosystems, and Management of Peatlands. The major finding of the workshop is that the organic soils are important in the overall carbon budget. Histosols and Gleysols, the major organic soil deposits of the world, normally sequester organic carbon fixed by plants. They may now be releasing enough carbon to account for nearly 10% of the annual rise in atmospheric content of CO/sub 2/.

  14. Organic Determinants of Learning and Behavioral Disorders.

    ERIC Educational Resources Information Center

    Philpott, William H.; And Others

    Theories regarding organic determinants of learning and behavior disorders are reviewed historically. Cases illustrating how a bio-ecologic examination can isolate the substances to which a person reacts and some of the reasons for those reactions are presented; and the role of various disorders in relation to the central nervous system is…

  15. Statistics provide guidance for indigenous organic carbon detection on Mars missions.

    PubMed

    Sephton, Mark A; Carter, Jonathan N

    2014-08-01

    Data from the Viking and Mars Science Laboratory missions indicate the presence of organic compounds that are not definitively martian in origin. Both contamination and confounding mineralogies have been suggested as alternatives to indigenous organic carbon. Intuitive thought suggests that we are repeatedly obtaining data that confirms the same level of uncertainty. Bayesian statistics may suggest otherwise. If an organic detection method has a true positive to false positive ratio greater than one, then repeated organic matter detection progressively increases the probability of indigeneity. Bayesian statistics also reveal that methods with higher ratios of true positives to false positives give higher overall probabilities and that detection of organic matter in a sample with a higher prior probability of indigenous organic carbon produces greater confidence. Bayesian statistics, therefore, provide guidance for the planning and operation of organic carbon detection activities on Mars. Suggestions for future organic carbon detection missions and instruments are as follows: (i) On Earth, instruments should be tested with analog samples of known organic content to determine their true positive to false positive ratios. (ii) On the mission, for an instrument with a true positive to false positive ratio above one, it should be recognized that each positive detection of organic carbon will result in a progressive increase in the probability of indigenous organic carbon being present; repeated measurements, therefore, can overcome some of the deficiencies of a less-than-definitive test. (iii) For a fixed number of analyses, the highest true positive to false positive ratio method or instrument will provide the greatest probability that indigenous organic carbon is present. (iv) On Mars, analyses should concentrate on samples with highest prior probability of indigenous organic carbon; intuitive desires to contrast samples of high prior probability and low prior

  16. Carbon accumulation in arid croplands of northwest China: pedogenic carbonate exceeding organic carbon

    PubMed Central

    Wang, Xiujun; Wang, Jiaping; Xu, Minggang; Zhang, Wenju; Fan, Tinglu; Zhang, Juan

    2015-01-01

    Soil carbonate (SIC) exceeds organic carbon (SOC) greatly in arid lands, thus may be important for carbon sequestration. However, field data for quantifying carbonate accumulation have been lacking. This study aims to improve our understanding of SIC dynamics and its role in carbon sequestration. We analyzed two datasets of SOC and SIC and their 13C compositions , one with over 100 soil samples collected recently from various land uses in the Yanqi Basin, Xinjiang, and the other with 18 archived soil samples from a long-term experiment (LTE) in Pingliang, Gansu. The data from the Yanqi Basin showed that SOC had a significant relationship with SIC and pedogenic carbonate (PIC); converting shrub land to cropland increased PIC stock by 5.2 kg C m−2, which was 3.6 times of that in SOC stock. The data from the LTE showed greater accumulation of PIC (21–49 g C m−2 year−1) than SOC (10–39 g C m−2 year−1) over 0–20 cm. Our study points out that intensive cropping in the arid and semi-arid regions leads to an increase in both SOC and PIC. Increasing SOC through straw organic amendments enhances PIC accumulation in the arid cropland of northwestern China. PMID:26091554

  17. Carbon accumulation in arid croplands of northwest China: pedogenic carbonate exceeding organic carbon

    NASA Astrophysics Data System (ADS)

    Wang, Xiujun; Wang, Jiaping; Xu, Minggang; Zhang, Wenju; Fan, Tinglu; Zhang, Juan

    2015-06-01

    Soil carbonate (SIC) exceeds organic carbon (SOC) greatly in arid lands, thus may be important for carbon sequestration. However, field data for quantifying carbonate accumulation have been lacking. This study aims to improve our understanding of SIC dynamics and its role in carbon sequestration. We analyzed two datasets of SOC and SIC and their 13C compositions , one with over 100 soil samples collected recently from various land uses in the Yanqi Basin, Xinjiang, and the other with 18 archived soil samples from a long-term experiment (LTE) in Pingliang, Gansu. The data from the Yanqi Basin showed that SOC had a significant relationship with SIC and pedogenic carbonate (PIC); converting shrub land to cropland increased PIC stock by 5.2 kg C m-2, which was 3.6 times of that in SOC stock. The data from the LTE showed greater accumulation of PIC (21-49 g C m-2 year-1) than SOC (10-39 g C m-2 year-1) over 0-20 cm. Our study points out that intensive cropping in the arid and semi-arid regions leads to an increase in both SOC and PIC. Increasing SOC through straw organic amendments enhances PIC accumulation in the arid cropland of northwestern China.

  18. Carbon accumulation in arid croplands of northwest China: pedogenic carbonate exceeding organic carbon.

    PubMed

    Wang, Xiujun; Wang, Jiaping; Xu, Minggang; Zhang, Wenju; Fan, Tinglu; Zhang, Juan

    2015-01-01

    Soil carbonate (SIC) exceeds organic carbon (SOC) greatly in arid lands, thus may be important for carbon sequestration. However, field data for quantifying carbonate accumulation have been lacking. This study aims to improve our understanding of SIC dynamics and its role in carbon sequestration. We analyzed two datasets of SOC and SIC and their (13)C compositions , one with over 100 soil samples collected recently from various land uses in the Yanqi Basin, Xinjiang, and the other with 18 archived soil samples from a long-term experiment (LTE) in Pingliang, Gansu. The data from the Yanqi Basin showed that SOC had a significant relationship with SIC and pedogenic carbonate (PIC); converting shrub land to cropland increased PIC stock by 5.2 kg C m(-2), which was 3.6 times of that in SOC stock. The data from the LTE showed greater accumulation of PIC (21-49 g C m(-2) year(-1)) than SOC (10-39 g C m(-2) year(-1)) over 0-20 cm. Our study points out that intensive cropping in the arid and semi-arid regions leads to an increase in both SOC and PIC. Increasing SOC through straw organic amendments enhances PIC accumulation in the arid cropland of northwestern China. PMID:26091554

  19. Export Fluxes of Dissolved Organic Carbon From the Yukon River

    NASA Astrophysics Data System (ADS)

    Guo, L.; Cai, Y.; Belzile, C.; MacDonald, R.

    2005-12-01

    Quantitative determination of export fluxes of carbon species through Arctic rivers is required to constrain the carbon budget in the Arctic Ocean and to understand the biogeochemical consequence of climate change in Northern drainage basins. In order to quantify the annual riverine export flux from the Yukon River, monthly or bimonthly water samples were collected at Pilot Station from July 2004 to July 2005 and analyzed for concentrations of dissolved organic carbon (DOC), particulate organic carbon (POC) and dissolved inorganic carbon (DIC). Concentration of DOC varied from 182 to 1683 uM (average 441 uM), with the highest concentration during river ice opening and the lowest in April under the ice. In contrast, DIC concentration increased from ice opening in May (1178 uM) to winter frozen season (2128 uM), with an average of 1588 uM. In addition to the DOC maximum during ice opening, an elevated DOC concentration was observed during the early stage of river ice formation, suggesting the rejection of DOC from ice during its formation. There was a positive correlation of DOC with freshwater flow rate whereas DIC correlated negatively with flow, indicating a hydrological control on both components but different source terms and transport mechanisms. Integrated annual export flux during 2004/2005 was 2.78x1012 g-C/y for DOC and 4.53x1012 g-C/y for DIC. Within the annual fluxes, only 5% of DOC and 17% of DIC were exported during the winter period when the river was frozen over. Long-term observations of DOC and DIC together with their molecular and isotopic signatures are needed to understand how the Yukon River Basin responds to a changing climate.

  20. Ecological determinism increases with organism size.

    PubMed

    Farjalla, Vinicius F; Srivastava, Diane S; Marino, Nicholas A C; Azevedo, Fernanda D; Dib, Viviane; Lopes, Paloma M; Rosado, Alexandre S; Bozelli, Reinaldo L; Esteves, Francisco A

    2012-07-01

    After much debate, there is an emerging consensus that the composition of many ecological communities is determined both by species traits, as proposed by niche theory, as well as by chance events. A critical question for ecology is, therefore, which attributes of species predict the dominance of deterministic or stochastic processes. We outline two hypotheses by which organism size could determine which processes structure ecological communities, and we test these hypotheses by comparing the community structure in bromeliad phytotelmata of three groups of organisms (bacteria, zooplankton, and macroinvertebrates) that encompass a 10 000-fold gradient in body size, but live in the same habitat. Bacteria had no habitat associations, as would be expected from trait-neutral stochastic processes, but still showed exclusion among species pairs, as would be expected from niche-based processes. Macroinvertebrates had strong habitat and species associations, indicating niche-based processes. Zooplankton, with body size between bacteria and macroinvertebrates, showed intermediate habitat associations. We concluded that a key niche process, habitat filtering, strengthened with organism size, possibly because larger organisms are both less plastic in their fundamental niches and more able to be selective in dispersal. These results suggest that the relative importance of deterministic and stochastic processes may be predictable from organism size. PMID:22919920

  1. Erosion of soil organic carbon: implications for carbon sequestration

    USGS Publications Warehouse

    Van Oost, Kristof; Van Hemelryck, Hendrik; Harden, Jennifer W.

    2009-01-01

    Agricultural activities have substantially increased rates of soil erosion and deposition, and these processes have a significant impact on carbon (C) mineralization and burial. Here, we present a synthesis of erosion effects on carbon dynamics and discuss the implications of soil erosion for carbon sequestration strategies. We demonstrate that for a range of data-based parameters from the literature, soil erosion results in increased C storage onto land, an effect that is heterogeneous on the landscape and is variable on various timescales. We argue that the magnitude of the erosion term and soil carbon residence time, both strongly influenced by soil management, largely control the strength of the erosion-induced sink. In order to evaluate fully the effects of soil management strategies that promote carbon sequestration, a full carbon account must be made that considers the impact of erosion-enhanced disequilibrium between carbon inputs and decomposition, including effects on net primary productivity and decomposition rates.

  2. Practical wet oxidation experiment to determine concentrations of particulate organic matter in seawater

    NASA Astrophysics Data System (ADS)

    Berger, V. Ya.; Mityaev, M. V.; Sukhotin, A. A.

    2016-03-01

    The report presents results of experiments testifying to the possibility of using wet oxidation to determine the concentrations of organic carbon in marine particulate matter. We describe a method for eliminating the measurement error caused by the influence of chlorides on the processes of dichromate oxidation of organic matter. We present an equation to calculate the concentration of organic carbon depending on that of sodium chloride.

  3. Pesticide sorption on geologic material of varying organic carbon content.

    PubMed

    Bouchard, D C; Wood, A L

    1988-09-01

    Sorption of three pesticides on geologic material ranging in organic carbon content from 0.33 to 6.9 g kg-1 was measured in soil columns using a miscible displacement technique. An octanol-water partitioning model was shown to be inappropriate for predicting sorption of the less hydrophobic pesticides on the low organic carbon materials. PMID:3255290

  4. Black Carbon in Estuarine and Coastal Ocean Dissolved Organic Matter

    NASA Technical Reports Server (NTRS)

    Mannino, Antonio; Harvey, H. Rodger

    2003-01-01

    Analysis of high-molecular-weight dissolved organic matter (DOM) from two estuaries in the northwest Atlantic Ocean reveals that black carbon (BC) is a significant component of previously uncharacterized DOM, suggesting that river-estuary systems are important exporters of recalcitrant dissolved organic carbon to the ocean.

  5. Radiocarbon dating of organic- and carbonate-carbon in Genyornis and Dromaius eggshell using stepped combustion and stepped acidification

    NASA Astrophysics Data System (ADS)

    Bird, M. I.; Turney, C. S. M.; Fifield, L. K.; Smith, M. A.; Miller, G. H.; Roberts, R. G.; Magee, J. W.

    2003-07-01

    A technique for determining the radiocarbon age of both organic-carbon and carbonate-carbon in the eggshell of the large flightless birds Genyornis newtoni (now extinct) and Dromaius novaehollandiae (extant emu) is presented here. Stepped combustion (for organic-carbon) and stepped acidification (for carbonate-carbon) were used to obtain multiple age determinations for each sample, from which an assessment of the reliability of the ages is possible. Analysis of a Genyornis newtoni eggshell fragment known to have an age considerably beyond the limit of radiocarbon dating has indicated that the backgrounds obtainable using this approach are 0.122±0.033 pMC for the organic-carbon fraction and 0.070±0.025 pMC for the carbonate-carbon fraction. These backgrounds suggest that finite ages up to 50,000-55,000 BP are readily achievable on eggshell using stepped combustion/acidification. Analysis of a single fragment of Genyornis eggshell from Williams Point, central South Australia, suggests that significant contamination of the organic-carbon fraction of the eggshell is possible, while ages for the carbonate fraction appear more reliable and indicate that the eggshell has an age of at least 49,000±2000 BP. A total of six analyses of single Genyornis newtoni and Dromaius novaehollandiae eggshell fragments from the Wood Point deposit in southern South Australia suggest ages for the samples of 41,000±800 and 37,900±700 BP, respectively, while an optically stimulated luminescence (OSL) sample from a location very close to the Genyornis sample has an age of 55±5 ka (1 σ). The OSL and calibrated radiocarbon ages for the Genyornis sample and the sand matrix overlap at two standard deviations, suggesting the most likely age for the eggshell and the sand matrix is ˜45 cal ka BP or earlier.

  6. Organic carbon hidden in urban ecosystems

    PubMed Central

    Edmondson, Jill L.; Davies, Zoe G.; McHugh, Nicola; Gaston, Kevin J.; Leake, Jonathan R.

    2012-01-01

    Urbanization is widely presumed to degrade ecosystem services, but empirical evidence is now challenging these assumptions. We report the first city-wide organic carbon (OC) budget for vegetation and soils, including under impervious surfaces. Urban soil OC storage was significantly greater than in regional agricultural land at equivalent soil depths, however there was no significant difference in storage between soils sampled beneath urban greenspaces and impervious surfaces, at equivalent depths. For a typical U.K. city, total OC storage was 17.6 kg m−2 across the entire urban area (assuming 0 kg m−2 under 15% of land covered by buildings). The majority of OC (82%) was held in soils, with 13% found under impervious surfaces, and 18% stored in vegetation. We reveal that assumptions underpinning current national estimates of ecosystem OC stocks, as required by Kyoto Protocol signatories, are not robust and are likely to have seriously underestimated the contributions of urban areas. PMID:23236585

  7. Organic carbon accumulation in Brazilian mangal sediments

    NASA Astrophysics Data System (ADS)

    Sanders, Christian J.; Smoak, Joseph M.; Sanders, Luciana M.; Sathy Naidu, A.; Patchineelam, Sambasiva R.

    2010-12-01

    This study reviews the organic carbon (OC) accumulation rates in mangrove forests, margins and intertidal mudflats in geographically distinct areas along the Brazilian coastline (Northeastern to Southern). Our initial results indicate that the mangrove forests in the Northeastern region of Brazil are accumulating more OC (353 g/m 2/y) than in the Southeastern areas (192 g/m 2/y) being that the sediment accumulation rates, 2.8 and 2.5 mm/y, and OC content ˜7.1% and ˜5.8% (dry sediment weight) were contributing factors to the discrepancies between the forests. The intertidal mudflats on the other hand showed substantially greater OC accumulation rates, sedimentation rates and content 1129 g/m 2/y and 234 g/m 2/y; 7.3 and 3.4 mm/y; 10.3% and ˜2.7% (OC of dry sediment weight content), respectively, in the Northeastern compared to the Southeastern region. Mangrove forests in the South-Southeastern regions of Brazil may be more susceptible to the rising sea level, as they are geographically constricted by the vast mountain ranges along the coastline.

  8. Net carbon flux in organic and conventional olive production systems

    NASA Astrophysics Data System (ADS)

    Saeid Mohamad, Ramez; Verrastro, Vincenzo; Bitar, Lina Al; Roma, Rocco; Moretti, Michele; Chami, Ziad Al

    2014-05-01

    Agricultural systems are considered as one of the most relevant sources of atmospheric carbon. However, agriculture has the potentiality to mitigate carbon dioxide mainly through soil carbon sequestration. Some agricultural practices, particularly fertilization and soil management, can play a dual role in the agricultural systems regarding the carbon cycle contributing to the emissions and to the sequestration process in the soil. Good soil and input managements affect positively Soil Organic Carbon (SOC) changes and consequently the carbon cycle. The present study aimed at comparing the carbon footprint of organic and conventional olive systems and to link it to the efficiency of both systems on carbon sequestration by calculating the net carbon flux. Data were collected at farm level through a specific and detailed questionnaire based on one hectare as a functional unit and a system boundary limited to olive production. Using LCA databases particularly ecoinvent one, IPCC GWP 100a impact assessment method was used to calculate carbon emissions from agricultural practices of both systems. Soil organic carbon has been measured, at 0-30 cm depth, based on soil analyses done at the IAMB laboratory and based on reference value of SOC, the annual change of SOC has been calculated. Substracting sequestrated carbon in the soil from the emitted on resulted in net carbon flux calculation. Results showed higher environmental impact of the organic system on Global Warming Potential (1.07 t CO2 eq. yr-1) comparing to 0.76 t CO2 eq. yr-1 in the conventional system due to the higher GHG emissions caused by manure fertilizers compared to the use of synthetic foliar fertilizers in the conventional system. However, manure was the main reason behind the higher SOC content and sequestration in the organic system. As a resultant, the organic system showed higher net carbon flux (-1.7 t C ha-1 yr-1 than -0.52 t C ha-1 yr-1 in the conventional system reflecting higher efficiency as a

  9. Inferring Absorbing Organic Carbon Content from AERONET Data

    NASA Technical Reports Server (NTRS)

    Arola, A.; Schuster, G.; Myhre, G.; Kazadzis, S.; Dey, S.; Tripathi, S. N.

    2011-01-01

    Black carbon, light-absorbing organic carbon (often called brown carbon) and mineral dust are the major light-absorbing aerosols. Currently the sources and formation of brown carbon aerosol in particular are not well understood. In this study we estimated globally the amount of light absorbing organic carbon and black carbon from AERONET measurements. We find that the columnar absorbing organic carbon (brown carbon) levels in biomass burning regions of South-America and Africa are relatively high (about 15-20 magnesium per square meters during biomass burning season), while the concentrations are significantly lower in urban areas in US and Europe. However, we estimated significant absorbing organic carbon amounts from the data of megacities of newly industrialized countries, particularly in India and China, showing also clear seasonality with peak values up to 30-35 magnesium per square meters during the coldest season, likely caused by the coal and biofuel burning used for heating. We also compared our retrievals with the modeled organic carbon by global Oslo CTM for several sites. Model values are higher in biomass burning regions than AERONET-based retrievals, while opposite is true in urban areas in India and China.

  10. Organic carbon inventories in natural and restored Ecuadorian mangrove forests

    PubMed Central

    Bruno, John F.; Benninger, Larry; Alperin, Marc; de Dios Morales, Juan

    2014-01-01

    Mangroves can capture and store organic carbon and their protection and therefore their restoration is a component of climate change mitigation. However, there are few empirical measurements of long-term carbon storage in mangroves or of how storage varies across environmental gradients. The context dependency of this process combined with geographically limited field sampling has made it difficult to generalize regional and global rates of mangrove carbon sequestration. This has in turn hampered the inclusion of sequestration by mangroves in carbon cycle models and in carbon offset markets. The purpose of this study was to estimate the relative carbon capture and storage potential in natural and restored mangrove forests. We measured depth profiles of soil organic carbon content in 72 cores collected from six sites (three natural, two restored, and one afforested) surrounding Muisne, Ecuador. Samples up to 1 m deep were analyzed for organic matter content using loss-on-ignition and values were converted to organic carbon content using an accepted ratio of 1.72 (g/g). Results suggest that average soil carbon storage is 0.055 ± 0.002 g cm−3 (11.3 ± 0.8% carbon content by dry mass, mean ± 1 SE) up to 1 m deep in natural sites, and 0.058 ± 0.002 g cm−3 (8.0 ± 0.3%) in restored sites. These estimates are concordant with published global averages. Evidence of equivalent carbon stocks in restored and afforested mangrove patches emphasizes the carbon sink potential for reestablished mangrove systems. We found no relationship between sediment carbon storage and aboveground biomass, forest structure, or within-patch location. Our results demonstrate the long-term carbon storage potential of natural mangroves, high effectiveness of mangrove restoration and afforestation, a lack of predictability in carbon storage strictly based on aboveground parameters, and the need to establish standardized protocol for quantifying mangrove sediment carbon stocks. PMID:24883249

  11. Organic carbon inventories in natural and restored Ecuadorian mangrove forests.

    PubMed

    DelVecchia, Amanda G; Bruno, John F; Benninger, Larry; Alperin, Marc; Banerjee, Ovik; de Dios Morales, Juan

    2014-01-01

    Mangroves can capture and store organic carbon and their protection and therefore their restoration is a component of climate change mitigation. However, there are few empirical measurements of long-term carbon storage in mangroves or of how storage varies across environmental gradients. The context dependency of this process combined with geographically limited field sampling has made it difficult to generalize regional and global rates of mangrove carbon sequestration. This has in turn hampered the inclusion of sequestration by mangroves in carbon cycle models and in carbon offset markets. The purpose of this study was to estimate the relative carbon capture and storage potential in natural and restored mangrove forests. We measured depth profiles of soil organic carbon content in 72 cores collected from six sites (three natural, two restored, and one afforested) surrounding Muisne, Ecuador. Samples up to 1 m deep were analyzed for organic matter content using loss-on-ignition and values were converted to organic carbon content using an accepted ratio of 1.72 (g/g). Results suggest that average soil carbon storage is 0.055 ± 0.002 g cm(-3) (11.3 ± 0.8% carbon content by dry mass, mean ± 1 SE) up to 1 m deep in natural sites, and 0.058 ± 0.002 g cm(-3) (8.0 ± 0.3%) in restored sites. These estimates are concordant with published global averages. Evidence of equivalent carbon stocks in restored and afforested mangrove patches emphasizes the carbon sink potential for reestablished mangrove systems. We found no relationship between sediment carbon storage and aboveground biomass, forest structure, or within-patch location. Our results demonstrate the long-term carbon storage potential of natural mangroves, high effectiveness of mangrove restoration and afforestation, a lack of predictability in carbon storage strictly based on aboveground parameters, and the need to establish standardized protocol for quantifying mangrove sediment carbon stocks. PMID:24883249

  12. First Molecular Dynamics simulation insight into the mechanism of organics adsorption from aqueous solutions on microporous carbons

    NASA Astrophysics Data System (ADS)

    Terzyk, Artur P.; Gauden, Piotr A.; Zieliński, Wojciech; Furmaniak, Sylwester; Wesołowski, Radosław P.; Klimek, Kamil K.

    2011-10-01

    The results of 84 MD simulations showing the influence of porosity and carbon surface oxidation on adsorption of three organic compounds from aqueous solutions on carbons are reported. Based on a model of 'soft' activated carbon, three carbon structures with gradually changed microporosity were created. Next, different number of surface oxygen groups was introduced. We observe quantitative agreement between simulation and experiment i.e. the decrease in adsorption from benzene down to paracetamol. Simulation results clearly demonstrate that the balance between porosity and carbon surface chemical composition in organics adsorption on carbons, and the pore blocking determine adsorption properties of carbons.

  13. Stable carbon isotope depth profiles and soil organic carbon dynamics in the lower Mississippi Basin

    USGS Publications Warehouse

    Wynn, J.G.; Harden, J.W.; Fries, T.L.

    2006-01-01

    Analysis of depth trends of 13C abundance in soil organic matter and of 13C abundance from soil-respired CO2 provides useful indications of the dynamics of the terrestrial carbon cycle and of paleoecological change. We measured depth trends of 13C abundance from cropland and control pairs of soils in the lower Mississippi Basin, as well as the 13C abundance of soil-respired CO2 produced during approximately 1-year soil incubation, to determine the role of several candidate processes on the 13C depth profile of soil organic matter. Depth profiles of 13C from uncultivated control soils show a strong relationship between the natural logarithm of soil organic carbon concentration and its isotopic composition, consistent with a model Rayleigh distillation of 13C in decomposing soil due to kinetic fractionation during decomposition. Laboratory incubations showed that initially respired CO 2 had a relatively constant 13C content, despite large differences in the 13C content of bulk soil organic matter. Initially respired CO2 was consistently 13C-depleted with respect to bulk soil and became increasingly 13C-depleted during 1-year, consistent with the hypothesis of accumulation of 13C in the products of microbial decomposition, but showing increasing decomposition of 13C-depleted stable organic components during decomposition without input of fresh biomass. We use the difference between 13C / 12C ratios (calculated as ??-values) between respired CO 2 and bulk soil organic carbon as an index of the degree of decomposition of soil, showing trends which are consistent with trends of 14C activity, and with results of a two-pooled kinetic decomposition rate model describing CO2 production data recorded during 1 year of incubation. We also observed inconsistencies with the Rayleigh distillation model in paired cropland soils and reasons for these inconsistencies are discussed. ?? 2005 Elsevier B.V. All rights reserved.

  14. Organic carbon flow in a swamp-stream ecosystem

    SciTech Connect

    Mulholland, P.J.

    1981-01-01

    An annual organic carbon budget is presented for an 8-km segment of Creeping Swamp, an undisturbed, third-order swamp-stream in the Coastal Plain of North Carolina, USA. Annual input of organic carbon (588 gC/m/sup 2/) was 96% allochthonous and was dominated by leaf litter inputs (36%) and fluvial, dissolved organic carbon (DOC) inputs (31%). Although the swamp-stream was primarily heterotrophic, autochthonous organic carbon input, primarily from filamentous algae, was important during February and March when primary production/ecosystem respiration (P/R) ratios of the flooded portions were near one. Annual output of organic carbon via fluvial processes (214 gC/m/sup 2/), 95% as DOC, was 36% of total annual inputs, indicating that the swamp-stream segment ecosystem was 64% efficient at retaining organic carbon. Organic carbon dynamics in the Creeping Swamp segment were compared to those reported for upland stream segments using indices of organic matter processing suggested by Fisher (1977) and a loading potential index suggested here. Creeping Swamp, while loading at a high rate, retains a much larger portion of its organic carbon inputs than two upland streams. Despite the high degree of retention and oxidation of organic inputs to Creeping Swamp, there is a net annual fluvial export of 21 gC/m/sup 2/, mostly in the dissolved form. Watersheds drained by swamp-streams in the southeastern United States are thought to have large organic carbon exports compared to upland forested drainages, because the stream network covers a much greater proportion of the total watershed area.

  15. Input related microbial carbon dynamic of soil organic matter in particle size fractions

    NASA Astrophysics Data System (ADS)

    Gude, A.; Kandeler, E.; Gleixner, G.

    2012-04-01

    This paper investigated the flow of carbon into different groups of soil microorganisms isolated from different particle size fractions. Two agricultural sites of contrasting organic matter input were compared. Both soils had been submitted to vegetation change from C3 (Rye/Wheat) to C4 (Maize) plants, 25 and 45 years ago. Soil carbon was separated into one fast-degrading particulate organic matter fraction (POM) and one slow-degrading organo-mineral fraction (OMF). The structure of the soil microbial community were investigated using phospholipid fatty acids (PLFA), and turnover of single PLFAs was calculated from the changes in their 13C content. Soil enzyme activities involved in the degradation of carbohydrates was determined using fluorogenic MUF (methyl-umbelliferryl phosphate) substrates. We found that fresh organic matter input drives soil organic matter dynamic. Higher annual input of fresh organic matter resulted in a higher amount of fungal biomass in the POM-fraction and shorter mean residence times. Fungal activity therefore seems essential for the decomposition and incorporation of organic matter input into the soil. As a consequence, limited litter input changed especially the fungal community favouring arbuscular mycorrhizal fungi. Altogether, supply and availability of fresh plant carbon changed the distribution of microbial biomass, the microbial community structure and enzyme activities and resulted in different priming of soil organic matter. Most interestingly we found that only at low input the OMF fraction had significantly higher calculated MRT for Gram-positive and Gram-negative bacteria suggesting high recycling of soil carbon or the use of other carbon sources. But on average all microbial groups had nearly similar carbon uptake rates in all fractions and both soils, which contrasted the turnover times of bulk carbon. Hereby the microbial carbon turnover was always faster than the soil organic carbon turnover and higher carbon input

  16. Temporal evolution of organic carbon concentrations in Swiss lakes: trends of allochthonous and autochthonous organic carbon.

    PubMed

    Rodríguez-Murillo, J C; Filella, M

    2015-07-01

    Evaluation of time series of organic carbon (OC) concentrations in lakes is useful for monitoring some of the effects of global change on lakes and their catchments. Isolating the evolution of autochthonous and allochthonous lake OC might be a useful way to differentiate between drivers of soil and photosynthetic OC related changes. However, there are no temporal series for autochthonous and allochthonous lake OC. In this study, a new approach has been developed to construct time series of these two categories of OC from existing dissolved organic carbon (DOC) data. First, temporal series (longer than ten years) of OC have been compiled for seven big Swiss lakes and another 27 smaller ones and evaluated by using appropriate non-parametric statistical methods. Subsequently, the new approach has been applied to construct time series of autochthonous and allochthonous lake OC in the seven big lakes. Doing this was possible because long term series of DOC concentrations at different depths are available for these lakes. Organic carbon concentrations generally increase in big lakes and decrease in smaller ones, although only in some cases are these trends statistically significant. The magnitude of the observed changes is generally small in big lakes (<1% annual change) and larger in smaller lakes. Autochthonous DOC concentrations in big lakes increase or decrease depending on the lake and the station but allochthonous DOC concentrations generally increase. This pattern is consistent with an increase in the OC input from the lakes' catchments and/or an increase in the refractoriness of the OC in question, and with a temporal evolution of autochthonous DOC depending on the degree of recovery from past eutrophication of each particular lake. In small lakes, OC dynamics are mainly driven by decreasing biological productivity, which in many, but not all cases, outweighs the probable increase of allochthonous OC. PMID:25782080

  17. Adsorption of selected volatile organic vapors on multiwall carbon nanotubes.

    PubMed

    Shih, Yang-hsin; Li, Mei-syue

    2008-06-15

    Carbon nanotubes are expected to play an important role in sensing, pollution treatment and separation techniques. This study examines the adsorption behaviors of volatile organic compounds (VOCs), n-hexane, benzene, trichloroethylene and acetone on two multiwall carbon nanotubes (MWCNTs), CNT1 and CNT2. Among these VOCs, acetone exhibits the highest adsorption capacity. The highest adsorption enthalpies and desorption energies of acetone were also observed. The strong chemical interactions between acetone and both MWCNTs may be the result from chemisorption on the topological defects. The adsorption heats of trichloroethylene, benzene, and n-hexane are indicative of physisorption on the surfaces of both MWCNTs. CNT2 presents a higher adsorption capacity than CNT1 due to the existence of an exterior amorphous carbon layer on CNT2. The amorphous carbon enhances the adsorption capacity of organic chemicals on carbon nanotubes. The morphological and structure order of carbon nanotubes are the primary affects on the adsorption process of organic chemicals. PMID:17980962

  18. Variation in assimilable organic carbon formation during chlorination of Microcystis aeruginosa extracellular organic matter solutions.

    PubMed

    Sun, Xingbin; Yuan, Ting; Ni, Huishan; Li, Yanpeng; Hu, Yang

    2016-07-01

    This study investigated the chlorination of Microcystis aeruginosa extracellular organic matter (EOM) solutions under different conditions, to determine how the metabolites produced by these organisms affect water safety and the formation of assimilable organic carbon (AOC). The effects of chlorine dosages, coagulant dosage, reaction time and temperature on the formation of AOC were investigated during the disinfection of M.aeruginosa metabolite solutions. The concentration of AOC followed a decreasing and then increasing pattern with increasing temperature and reaction time. The concentration of AOC decreased and then increased with increasing chlorination dosage, followed by a slight decrease at the highest level of chlorination. However, the concentration of AOC decreased continuously with increasing coagulant dosage. The formation of AOC can be suppressed under appropriate conditions. In this study, chlorination at 4mg/L, combined with a coagulant dose of 40mg/L at 20°C over a reaction time of 12hr, produced the minimum AOC. PMID:27372113

  19. Determination of soil organic phosphorus exchange sensitivity

    NASA Astrophysics Data System (ADS)

    Shand, Charles; Wendler, Renate; Lumsdon, David; Cooper, Pat; George, Timothy; Brown, Lawrie; Giles, Courtney; Stutter, Marc; Menezes-Blackburn, Daniel; Zhang, Hao; Wearing, Catherine; Haygarth, Philip; Blackwell, Martin; Darch, Tegan

    2015-04-01

    Soils contain both organic and inorganic phosphorus (P) species in varying proportions. Studies have shown that many soils contain substantial amounts of inositol hexaphosphate (IHP) and there is much interest worldwide in developing strategies to make some use of this recalcitrant resource for plant growth to reduce P fertilizer inputs. Little is known about the preference of ion exchange processes in the solubilisation of organic vs inorganic P forms in soils, an important first step in making P forms bioavailable. Although they do not possess biotic functions, resins provides a simple means to deplete P forms in soil allowing investigation of exchange selectivity between inorganic and organic P forms. The aim of our work was to determine new understanding of exchange selectivity in soils and provide insight into potential depletion and plant uptake of soil phosphorus, with emphasis on organic forms such as IHP. For our study we used a Cambisol sampled from an agricultural area (Tayport) near Dundee in Scotland. The soil had a high Olsen (0.5 M sodium bicarbonate at pH 8.5) extractable P status (84 mg P/kg) and P-31 nuclear magnetic resonance analysis of its NaOH/EDTA extract showed it contained a substantial proportion of IHP (21 % of total extractable P). For resin extraction we used anion exchange resin sheets (4.17 cm each side) in bicarbonate form to minimise pH related solubilisation effects. We used 3.5 g of soil in 75 ml of water and added 1, 2 or 3 resin squares. After equilibration the resin squares were removed and replaced with fresh resin squares a further 3 times. Phosphorus was recovered from the resin sheets by elution with 0.25 M sulphuric acid and analysed by inductively coupled plasma spectroscopy to determine total P, and colorimetrically with malachite green to determine inorganic P with the remainder assigned to organic P. The data showed that the resin preferentially removed inorganic P and even after four sequential extractions little or

  20. Important role for organic carbon in subduction-zone fluids in the deep carbon cycle

    NASA Astrophysics Data System (ADS)

    Sverjensky, Dimitri A.; Stagno, Vincenzo; Huang, Fang

    2014-12-01

    Supercritical aqueous fluids link subducting plates and the return of carbon to Earth's surface in the deep carbon cycle. The amount of carbon in the fluids and the identities of the dissolved carbon species are not known, which leaves the deep carbon budget poorly constrained. Traditional models, which assume that carbon exists in deep fluids as dissolved gas molecules, cannot predict the solubility and ionic speciation of carbon in its silicate rock environment. Recent advances enable these limitations to be overcome when evaluating the deep carbon cycle. Here we use the Deep Earth Water theoretical model to calculate carbon speciation and solubility in fluids under upper mantle conditions. We find that fluids in equilibrium with mantle peridotite minerals generally contain carbon in a dissolved gas molecule form. However, fluids in equilibrium with diamonds and eclogitic minerals in the subducting slab contain abundant dissolved organic and inorganic ionic carbon species. The high concentrations of dissolved carbon species provide a mechanism to transport large amounts of carbon out of the subduction zone, where the ionic carbon species may influence the oxidation state of the mantle wedge. Our results also identify novel mechanisms that can lead to diamond formation and the variability of carbon isotopic composition via precipitation of the dissolved organic carbon species in the subduction-zone fluids.

  1. Environmental analyse of soil organic carbon stock changes in Slovakia

    NASA Astrophysics Data System (ADS)

    Koco, Š.; Barančíková, G.; Skalský, R.; Tarasovičová, Z.; Gutteková, M.; Halas, J.; Makovníková, J.; Novákova, M.

    2012-04-01

    still growing. At colder agroclimatic regions, at flysch region especially where cambisols are present with low of SOM stability since 1994 stability or decreasing of SOC stock is resulting. This is result of climatic impact (lower temperatures, higher humidity) as well as the way of soil management because at colder region the number of glasslands is increased in comparison to arable land. Close relationship between SOC stock and soil production potential index representing the official basis for soil quality evaluation in Slovakia was also determined and a polynomial model was found which describes the relation at the 95% confidence level. From the obtained results it can be concluded, that the amount of crop residues and farmyard manure coming to the soil both in the first and second simulation period (1970 - 1995 and 1996 - 2007) was responsible for general trends in SOC stock dynamics. Achieved results also show different amount and changes of SOC stock in different agroclimatic regions. It was also found that that value of soil production potential index generally used for soil quality assessment in Slovakia corresponds well with simulated values of SOC stocks in top-soils of cropland soils. Key words Soil organic carbon stock, modelling, agricultural soils, agroclimatic regions, Slovakia Acknowledgements This work was supported by the Slovak Research and Development Agency under the contract No. APVV-0333-06.

  2. SAMPLING DURATION DEPENDENCE OF SEMI-CONTINUOUS ORGANIC CARBON MEASUREMENTS ON STEADY STATE SECONDARY ORGANIC AEROSOLS

    EPA Science Inventory

    Semi-continuous organic carbon concentrations were measured through several experiments of statically generated secondary organic aerosol formed by hydrocarbon + NOx irradiations. Repeated, randomized measurements of these steady state aerosols reveal decreases in the observed c...

  3. Variations in dissolved organic carbon concentrations across peatland hillslopes

    NASA Astrophysics Data System (ADS)

    Boothroyd, I. M.; Worrall, F.; Allott, T. E. H.

    2015-11-01

    Peatlands are important terrestrial carbon stores and dissolved organic carbon (DOC) is one of the most important contributors to carbon budgets in peatland systems. Many studies have investigated factors affecting DOC concentration in peatland systems, yet hillslope position has been thus far overlooked as a variable that could influence DOC cycling. This study investigates the importance of hillslope position with regard to DOC cycling. Two upland peat hillslopes were studied in the Peak District, UK, to determine what impact, if any, hillslope position had upon DOC concentration. Hillslope position was found to be a significant factor affecting variation in soil pore water DOC concentration, with bottom-slope positions having significantly lower DOC concentrations than up-slope because of dilution of DOC as water moves down-slope and is flushed out of the system via lateral throughflow. Water table drawdown on steeper mid-slopes increased DOC concentrations through increased DOC production and extended residence times allowing a build-up of humic-rich DOC compounds. Hillslope position did not significantly affect DOC concentrations in surface runoff water because of the dilution of near-surface soil pore water by precipitation inputs, while stream water had similar water chemistry properties to soil pore water under low-flow conditions.

  4. Organic carbon isotope constraints on the dissolved organic carbon (DOC) reservoir at the Cryogenian-Ediacaran transition

    NASA Astrophysics Data System (ADS)

    Jiang, Ganqing; Wang, Xinqiang; Shi, Xiaoying; Zhang, Shihong; Xiao, Shuhai; Dong, Jin

    2010-10-01

    Prominent negative carbonate carbon isotope (δ 13C carb) anomalies from some Ediacaran successions are accompanied by invariant or decoupled organic carbon isotope (δ 13C org) values and have been interpreted as resulting from the remineralization of a large dissolved organic carbon (DOC) reservoir capable of buffering carbon isotopes of organic matter. This inferred oceanic DOC reservoir was thought to have initiated with the onset of Cryogenian glaciations (ca. 720 Ma) and lasted for millions of years until the late Ediacaran Period (< 560 Ma). Carbon isotope analyses of the basal Doushantuo Formation (ca. 635 Ma) in south China reveal that (1) the cap carbonate has δ 13C org around -26‰ (VPDB) and relatively low Δδ 13C (22 ± 2‰) and (2) the overlying organic-rich black shale and shaly dolostone have more negative δ 13C org (-28‰ to -35‰) and higher Δδ 13C (28‰-30‰). Both δ 13C carb and δ 13C org show a + 6‰ shift within a 4-m-thick interval overlying the Doushantuo cap carbonate. The δ 13C org values of the cap carbonate are associated with low TOC (mostly < 0.1%); their paleoceanographic significance requires further tests in other Ediacaran basins. The co-varying positive shift in δ 13C carb and δ 13C org following cap carbonate deposition is best interpreted as resulting from a rapid increase in organic carbon burial, which may have resulted in the rise of oxygen and heralded the first appearance of animals a few meters above the Doushantuo cap carbonate. The data suggest that a large oceanic DOC reservoir did not exist in the early Ediacaran ocean. Excess oceanic DOC required to explain the Ediacaran Shuram and upper Doushantuo δ 13C excursions, if it existed, had to be developed during the Ediacaran Period after cap carbonate deposition.

  5. Soil organic carbon enrichment of dust emissions: Magnitude, mechanisms and its implications for the carbon cycle

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soil erosion is an important component of the global carbon cycle. However, little attention has been given to the role of aeolian processes in influencing soil organic carbon (SOC) flux and the release of greenhouse gasses, such as carbon-dioxide (CO2), to the atmosphere. Understanding the magnitu...

  6. Limits to soil carbon stability; Deep, ancient soil carbon decomposition stimulated by new labile organic inputs

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soil carbon (C) pools store about one-third of the total terrestrial organic carbon. Deep soil C pools (below 1 m) are thought to be stable due to their low biodegradability, but little is known about soil microbial processes and carbon dynamics below the soil surface, or how global change might aff...

  7. [Effects of Chinese fir litter on soil organic carbon decomposition and microbial biomass carbon].

    PubMed

    Wang, Xiao-Feng; Wang, Si-Long; Zhang, Wei-Dong

    2013-09-01

    By using 13C stable isotope tracer technique, this paper studied the effects of Chinese fir litter addition on the soil organic carbon (SOC) decomposition, microbial biomass carbon, and dissolved organic carbon in 0-5 cm and 40-45 cm layers. The decomposition rate of SOC in 40-45 cm layer was significantly lower than that in 0-5 cm layer, but the priming effect induced by the Chinese fir litter addition showed an opposite trend. The Chinese fir litter addition increased the soil total microbial biomass carbon and the microbial biomass carbon derived from native soil significantly, but had less effects on the soil dissolved organic carbon. Turning over the subsoil to the surface of the woodland could accelerate the soil carbon loss in Chinese fir plantation due to the priming effect induced by the litters. PMID:24417093

  8. Evaluation of organic carbon analyzers for space application. [for water reclamation

    NASA Technical Reports Server (NTRS)

    1984-01-01

    The state-of-the-art technology for organic carbon analysis in space applications is evaluated. An investigation into total organic carbon (TOC) analysis has identified a variety of schemes which include different methods for: (1) separation of inorganic carbon from organic carbon and/or differentiation of inorganic carbon from organic carbon; (2) reaction of organic carbon to form a quantifiable species; and (3) detection and measurement of that species. Each method option is discussed.

  9. Carbon nanotube-based organic light emitting diodes

    NASA Astrophysics Data System (ADS)

    Bansal, Malti; Srivastava, Ritu; Lal, C.; Kamalasanan, M. N.; Tanwar, L. S.

    2009-11-01

    Carbon nanotubes; revolutionary and fascinating from the materials point of view and exceedingly sensational from a research point of view; are standing today at the threshold between inorganic electronics and organic electronics and posing a serious challenge to the big daddies of these two domains in electronics i.e., silicon and indium tin oxide (ITO). In the field of inorganic electronics, carbon nanotubes offer advantages such as high current carrying capacity, ballistic transport, absence of dangling bonds, etc. and on the other hand, in the field of organic electronics, carbon nanotubes offer advantages such as high conductivity, high carrier mobility, optical transparency (in visible and IR spectral ranges), flexibility, robustness, environmental resistance, etc. and hence, they are seriously being considered as contenders to silicon and ITO. This review traces the origin of carbon nanotubes in the field of organic electronics (with emphasis on organic light emitting diodes) and moves on to cover the latest advances in the field of carbon nanotube-based organic light emitting diodes. Topics that are covered within include applications of multi-wall nanotubes and single-wall nanotubes in organic light emitting diodes. Applications of carbon nanotubes as hole-transport layers, as electron-transport layers, as transparent electrodes, etc. in organic light emitting diodes are discussed and the daunting challenges facing this progressive field today are brought into the limelight.

  10. A reduced organic carbon component in martian basalts.

    PubMed

    Steele, A; McCubbin, F M; Fries, M; Kater, L; Boctor, N Z; Fogel, M L; Conrad, P G; Glamoclija, M; Spencer, M; Morrow, A L; Hammond, M R; Zare, R N; Vicenzi, E P; Siljeström, S; Bowden, R; Herd, C D K; Mysen, B O; Shirey, S B; Amundsen, H E F; Treiman, A H; Bullock, E S; Jull, A J T

    2012-07-13

    The source and nature of carbon on Mars have been a subject of intense speculation. We report the results of confocal Raman imaging spectroscopy on 11 martian meteorites, spanning about 4.2 billion years of martian history. Ten of the meteorites contain abiotic macromolecular carbon (MMC) phases detected in association with small oxide grains included within high-temperature minerals. Polycyclic aromatic hydrocarbons were detected along with MMC phases in Dar al Gani 476. The association of organic carbon within magmatic minerals indicates that martian magmas favored precipitation of reduced carbon species during crystallization. The ubiquitous distribution of abiotic organic carbon in martian igneous rocks is important for understanding the martian carbon cycle and has implications for future missions to detect possible past martian life. PMID:22628557

  11. Floodplain Organic Carbon Storage in the Central Yukon River Basin

    NASA Astrophysics Data System (ADS)

    Lininger, K.; Wohl, E.

    2014-12-01

    Floodplain storage of organic carbon is an important aspect of the global carbon cycle that is not well understood or quantified. Although it is understood that rivers transport organic carbon to the ocean, little is known about the quantity of stored carbon in boreal floodplains and the influence of fluvial processes on this storage. We present results on total organic carbon (TOC) content within the floodplains of two rivers, the Dall River and Preacher Creek, in the central Yukon River Basin in the Yukon Flats National Wildlife Refuge of Alaska. The results indicate that organic carbon storage is influenced by fluvial disturbance and grain size. The Dall River, which contains a large amount of floodplain carbon, is meandering and incised, with well-developed floodplain soils, a greater percentage of relatively old floodplain surfaces and a slower floodplain turnover time, and finer grain sizes. Preacher Creek stores less TOC, transports coarser grain sizes, and has higher rates of avulsion and floodplain turnover time. Within the floodplain of a particular river, large spatial heterogeneity in TOC content also exists as a function of depositional environment and age and vegetation community of the site. In addition, saturated regions of the floodplains, such as abandoned channels and oxbow lakes, contain more TOC compared to drier floodplain environments. Frozen alluvial soils likely contain carbon that could be released into the environment with melting permafrost, and thus quantifying the organic carbon content in the active layer of floodplain soils could provide insight into the characteristics of the permafrost beneath. The hydrology in these regions is changing due to permafrost melt, and floodplain areas usually saturated could be dried out, causing breakdown and outgassing of carbon stored in previously saturated soils. Ongoing work will result in a first-order estimate of active-layer floodplain carbon storage for the central Yukon River Basin.

  12. Variations of organic carbon stock in reclaimed estuarine soils (Villaviciosa estuary, NW Spain).

    PubMed

    Santín, Cristina; Otero, Xose Luis; Fernández, Susana; González-Pérez, Martha; Alvarez, Miguel Angel

    2007-05-25

    A study was carried out in the Villaviciosa Estuary (Asturias, NW Spain) to determine the effects of polderization on soil properties and soil organic carbon content. The results showed that the polderized soils were more acidic and contained less carbonates and a higher soil organic carbon (SOC) content than the natural soils. The organic carbon stock in the reclaimed soils ranged from 83.2 to 91.8 t ha(-1), whereas in natural soils was approximately 43.7 t ha(-1). The degree of humification of the surface humic acids also indicated that the stability and degree of decomposition of the organic matter was higher in the reclaimed soils than in natural soils. PMID:17374546

  13. Anomalous 13C enrichment in modern marine organic carbon

    USGS Publications Warehouse

    Arthur, M.A.; Dean, W.E.; Claypool, G.E.

    1985-01-01

    Marine organic carbon is heavier isotopically (13C enriched) than most land-plant or terrestrial organic C1. Accordingly, ??13C values of organic C in modern marine sediments are routinely interpreted in terms of the relative proportions of marine and terrestrial sources of the preserved organic matter2,3. When independent geochemical techniques are used to evaluate the source of organic matter in Cretaceous or older rocks, those rocks containing mostly marine organic C are found typically to have lighter (more-negative) ??13C values than rocks containing mostly terrestrial organic C. Here we conclude that marine photosynthesis in mid-Cretaceous and earlier oceans generally resulted in a greater fractionation of C isotopes and produced organic C having lighter ??13C values. Modern marine photosynthesis may be occurring under unusual geological conditions (higher oceanic primary production rates, lower PCO2) that limit dissolved CO2 availability and minimize carbon isotope fractionation4. ?? 1985 Nature Publishing Group.

  14. Unimodal response of fish yield to dissolved organic carbon.

    PubMed

    Finstad, Anders G; Helland, Ingeborg P; Ugedal, Ola; Hesthagen, Trygve; Hessen, Dag O

    2014-01-01

    Here, we demonstrate a contrasting effect of terrestrial coloured dissolved organic material on the secondary production of boreal nutrient poor lakes. Using fish yield from standardised brown trout gill-net catches as a proxy, we show a unimodal response of lake secondary productivity to dissolved organic carbon (DOC). This suggests a trade-off between positive and negative effects, where the initial increase may hinge upon several factors such as energy subsidising, screening of UV-radiation or P and N load being associated with organic carbon. The subsequent decline in production with further increase in DOC is likely associated with light limitations of primary production. We also show that shallow lakes switch from positive to negative effects at higher carbon loads than deeper lakes. These results underpin the major role of organic carbon for structuring productivity of boreal lake ecosystems. PMID:24165396

  15. PREDICTING PREFERENTIAL ADSORPTION OF ORGANICS BY ACTIVATED CARBON

    EPA Science Inventory

    Preferential adsorption of organic compounds onto activated carbon from dilute aqueous solutions was studied to develop a comprehensive theoretical basis for predicting adsorption of multicomponent solutes. The research program investigates why some solutes are strong adsorbers, ...

  16. Dissolved organic carbon and its potential predictors in eutrophic lakes.

    PubMed

    Toming, Kaire; Kutser, Tiit; Tuvikene, Lea; Viik, Malle; Nõges, Tiina

    2016-10-01

    Understanding of the true role of lakes in the global carbon cycle requires reliable estimates of dissolved organic carbon (DOC) and there is a strong need to develop remote sensing methods for mapping lake carbon content at larger regional and global scales. Part of DOC is optically inactive. Therefore, lake DOC content cannot be mapped directly. The objectives of the current study were to estimate the relationships of DOC and other water and environmental variables in order to find the best proxy for remote sensing mapping of lake DOC. The Boosted Regression Trees approach was used to clarify in which relative proportions different water and environmental variables determine DOC. In a studied large and shallow eutrophic lake the concentrations of DOC and coloured dissolved organic matter (CDOM) were rather high while the seasonal and interannual variability of DOC concentrations was small. The relationships between DOC and other water and environmental variables varied seasonally and interannually and it was challenging to find proxies for describing seasonal cycle of DOC. Chlorophyll a (Chl a), total suspended matter and Secchi depth were correlated with DOC and therefore are possible proxies for remote sensing of seasonal changes of DOC in ice free period, while for long term interannual changes transparency-related variables are relevant as DOC proxies. CDOM did not appear to be a good predictor of the seasonality of DOC concentration in Lake Võrtsjärv since the CDOM-DOC coupling varied seasonally. However, combining the data from Võrtsjärv with the published data from six other eutrophic lakes in the world showed that CDOM was the most powerful predictor of DOC and can be used in remote sensing of DOC concentrations in eutrophic lakes. PMID:27318445

  17. Real World of Industrial Chemistry: Organic Chemicals from Carbon Monoxide.

    ERIC Educational Resources Information Center

    Kolb, Kenneth E.; Kolb, Doris

    1983-01-01

    Carbon Monoxide obtained from coal may serve as the source for a wide variety of organic compounds. Several of these compounds are discussed, including phosgene, benzaldehyde, methanol, formic acid and its derivatives, oxo aldehydes, acrylic acids, and others. Commercial reactions of carbon monoxide are highlighted in a table. (JN)

  18. Black carbon and organic matter stabilization in soil

    NASA Astrophysics Data System (ADS)

    Lehmann, J.; Liang, B.; Sohi, S.; Gaunt, J.

    2007-12-01

    Interaction with minerals is key to stabilization of organic matter in soils. Stabilization is commonly perceived to occur due to entrapment in pore spaces, encapsulation within aggregates or interaction with mineral surfaces. Typically only interactions between organic matter and minerals are considered in such a model. Here we demonstrate that black carbon may act very similar to minerals in soil in that it enhances the stabilization of organic matter. Mineralization of added organic matter was slower and incorporation into intra-aggregate fractions more rapid in the presence of black carbon. Added double-labeled organic matter was recovered in fractions with high amounts of black carbon. Synchrotron-based near-edge x-ray fine structure (NEXAFS) spectroscopy coupled to scanning transmission x-ray microscopy (STXM) suggested a possible interaction of microorganisms with black carbon surfaces and metabolization of residues. These findings suggest a conceptual model that includes carbon-carbon interactions and by-passing for more rapid stabilization of litter into what is commonly interpreted as stable carbon pools.

  19. Maturation of organic matter during experimental simulation of carbonate diagenesis

    SciTech Connect

    Ferguson, J.; Bush, P.R.; Clarke, B.A. )

    1989-09-01

    An earlier investigation involving the simulation of the early stages of diagenesis of carbonate ooids has been extended to include skeletal carbonates and carbonate mud. The experiments, lasting up to 70 days at elevated hydrostatic pressure and temperatures of 180{degree}-210{degree}C, used natural sea water and recent calcitic and aragonitic carbonate materials collected from Florida Bay and the Bahamas. The results give insight into the processes of maturation and diagenesis of the organic and inorganic fractions. Analysis of the organic fraction, both before and after the experiments, gives indicates of possible pathways of maturation during early diagenesis. A small amount of data is also available on the fate of sugars and amino acids in the system. Overall, the experiments closely approximate the natural system. Reactions occurring in the inorganic components are closely allied to those in the organic fraction. Indeed, two of the critical factors in early carbonate diagenesis are the amount and quality of organic matter and the shape, size, and nature of the carbonate grains. Changes in the carbonate fraction taking place during and after the experiments have been deduced by monitoring the pore fluid chemistry and by analyzing the final solid product. These results are discussed briefly and related to changes in the organic phase.

  20. Implications of Different Worldviews to Assess Soil Organic Carbon Change

    NASA Astrophysics Data System (ADS)

    Grunwald, S.

    2012-04-01

    Profound shifts have occurred over the last three centuries in which human actions have become the main driver to global environmental change. In this new epoch, the Anthropocene, human-driven changes such as climate and land use change, are pushing the Earth system well outside of its normal operating range causing severe and abrupt environmental change. Changes in land use management and land cover are intricately linked to the carbon cycle, but our knowledge on its spatially and temporally explicit impact on carbon dynamics across different scales is still poorly understood. To elucidate on the magnitude of change in soil organic carbon (SOC) due to human-induced stressors different philosophical worldviews may be considered including (i) empiricism - direct measurements of properties and processes at micro, site-specific or field scales; (ii) metaphysics and ontology - conceptual models to assess soil change (e.g., STEP-AWBH); (iii) epistemology - indirect approaches (e.g., meta-analysis or spectral informed prediction models); (iv) reductionism - e.g., carbon flux measurements; (iv) determinism - mechanistic simulation models and biogeochemical investigations (e.g., Century or DNDC); (v) holism - national or global soil databases and aggregate maps; or (vi) integral - fusing individual, social, economic, cultural and empirical perspectives. The strengths and limitations of each of these philosophical approaches are demonstrated using case examples from Florida and U.S.A. The sensitivity to assess SOC change and uncertainty, backcasting and forecasting ability, scaling potential across space and time domains, and limitations and constraints of different worldviews are discussed.

  1. Determinants of stagnating carbon intensity in China

    NASA Astrophysics Data System (ADS)

    Guan, Dabo; Klasen, Stephan; Hubacek, Klaus; Feng, Kuishuang; Liu, Zhu; He, Kebin; Geng, Yong; Zhang, Qiang

    2014-11-01

    China committed itself to reduce the carbon intensity of its economy (the amount of CO2 emitted per unit of GDP) by 40-45% during 2005-2020. Yet, between 2002 and 2009, China experienced a 3% increase in carbon intensity, though trends differed greatly among its 30 provinces. Decomposition analysis shows that sectoral efficiency gains in nearly all provinces were offset by movement towards a more carbon-intensive economic structure. Such a sectoral shift seemed to be heavily affected by the growing role of investments and capital accumulation in China's growth process which has favoured sectors with high carbon intensity. Panel data regressions show that changes in carbon intensity were smallest in sectors dominating the regional economy (so as not to endanger these large sectors, which are the mainstay of the provincial economy), whereas scale and convergence effects played a much smaller role.

  2. RT-MATRIX: Measuring Total Organic Carbon by Photocatalytic Oxidation of Volatile Organic Compounds

    NASA Technical Reports Server (NTRS)

    2008-01-01

    Volatile organic compounds (VOCs) inevitably accumulate in enclosed habitats such as the International Space Station and the Crew Exploration Vehicle (CEV) as a result of human metabolism, material off-gassing, and leaking equipment. Some VOCs can negatively affect the quality of the crew's life, health, and performance; and consequently, the success of the mission. Air quality must be closely monitored to ensure a safe living and working environment. Currently, there is no reliable air quality monitoring system that meets NASA's stringent requirements for power, mass, volume, or performance. The ultimate objective of the project -- the development of a Real-Time, Miniaturized, Autonomous Total Risk Indicator System (RT.MATRIX).is to provide a portable, dual-function sensing system that simultaneously determines total organic carbon (TOC) and individual contaminants in air streams.

  3. Investigation of organic carbon transformation in soils of dominant dissolved organic carbon source zones

    NASA Astrophysics Data System (ADS)

    Pissarello, Anna; Miltner, Anja; Oosterwoud, Marieke; Fleckenstein, Jan; Kästner, Matthias

    2014-05-01

    Over the past 20 years both a decrease in soil organic matter (SOM) and an increase in the dissolved organic carbon (DOC) concentrations in surface water bodies, including drinking water reservoirs, have been recorded in the northern hemisphere. This development has severe consequences for soil fertility and for drinking water purification. As both processes occur simultaneously, we assume that microbial SOM degradation, which transforms SOM into CO2 and DOC, is a possible source of the additional DOC in the surface water. In addition we speculate that both processes are initially triggered by physical mechanisms, resulting in a modification of the organic matter solubility equilibria and thus in higher SOM availability and DOC mobilization. The general hypothesis of the study is therefore that SOM loss and DOC increase are combined consequences of enhanced microbial degradation of SOM and that this is a result of climate variations and global change, e.g. the increase of the temperature, the alteration of the water regime (i.e. increase of the frequency of drying and rewetting cycles and a higher number of heavy rain events), but also the decrease of the atmospheric acid deposition resulting in an increase of soil pH values. The general goal of the study is the identification of the dominant processes and controlling factors involved in soil microbial carbon turnover and mobilization of DOC in soils from catchment areas that contribute DOC to the receiving waters and the downstream Rappbode reservoir, which showed a pronounced increase in DOC concentration in recent years. This reservoir is the source of drinking water for about one million people in northern Germany. Preliminary screening experiments, consisting of 65-day soil batch incubation experiments, have been conducted in order to select the parameters (and the parameter ranges) of relevance for further in-depth experiments. During the experiments, different soil systems were exposed to different

  4. Carbon isotopic studies of organic matter in Precambrian rocks.

    NASA Technical Reports Server (NTRS)

    Oehler, D. Z.; Schopf, J. W.; Kvenvolden, K. A.

    1972-01-01

    A survey has been undertaken of the carbon composition of the total organic fraction of a suite of Precambrian sediments to detect isotopic trends possibly correlative with early evolutionary events. Early Precambrian cherts of the Fig Tree and upper and middle Onverwacht groups of South Africa were examined for this purpose. Reduced carbon in these cherts was found to be isotopically similar to photosynthetically produced organic matter of younger geological age. Reduced carbon in lower Onverwacht cherts was found to be anomalously heavy; it is suggested that this discontinuity may reflect a major event in biological evolution.

  5. Photochemical Control of Organic Carbon Availability to Coastal Microbial Communities

    NASA Astrophysics Data System (ADS)

    Miller, W. L.; Reader, H. E.; Powers, L. C.

    2010-12-01

    Chromophoric dissolved organic matter (CDOM) is the fraction of dissolved organic matter that absorbs solar radiation. In terrestrially influenced locations high concentrations of CDOM help to shield the biological community from harmful UV radiation. Although CDOM is largely biologically refractory in nature, photochemistry has the potential to transform biologically refractory carbon into more biolabile forms. Studies suggest that in marine systems, the effect of UVR on carbon availability and subsequent bacterial production varies widely, ranging from a +200% increase to a -75% decrease (Mopper and Kieber, 2002). Evidence suggests that the largely negative or “no-effect” samples are from oligotrophic waters and that terrestrially influenced samples experience a more positive effect on the biolability of carbon after irradiation. To quantify the effects of photochemistry on the biolability of DOC in a terrestrially influenced system, a quarterly sampling effort was undertaken at three estuarine locations off the coast of Georgia, USA for a total of 14 apparent quantum yield (AQY) determinations. Large expanses of salt marsh on the coast of Georgia, create a large non-point source of DOC to the coastal ocean. Sapelo Sound, the northernmost sampling site, is dominated by offshore waters and receives little to no freshwater input throughout the year. Altamaha Sound, the southernmost sampling site, is strongly influenced by the Altamaha River, which drains the largest watershed in the state of Georgia. Doboy Sound, situated between these two sites, is largely marine dominated but is influenced by fresh water during periods of high river flow. Each sample was 0.2um filter-sterilized before irradiation in a Suntest Solar Simulator; using optical filters to create 7 distinct radiance spectra in 15 samples for determination of AQY spectra for release of biolabile DOC. Irradiated samples were consequently inoculated with the natural microbial community concentrated

  6. [Relationships between soil organic carbon and environmental factors in gully watershed of the Loess Plateau].

    PubMed

    Wei, Xiao-Rong; Shao, Ming-An; Gao, Jian-Lun

    2008-10-01

    Understanding the distribution of organic carbon fractions in soils and their relationships with environmental factors are very important for appraising soil organic carbon status and assessing carbon cycling in the Loess Plateau. In this research, through field investigation and laboratory analysis, we studied the relationships between soil organic carbon and environmental factors in a gully watershed of the Loess Plateau. The environmental factors are landforms, land use conditions and soil types. The results showed that total soil organic carbon presented less variance, while high labile organic carbon presented greater variance. The variation coefficients of them are 34% and 43%, respectively, indicating that the variability of organic carbon in soils increased with the increasing of their activities. Total soil organic carbon, labile organic carbon, middle and high labile organic carbon were highly interrelated and presented similar distribution trend with environmental factors. Among different landforms, land uses, and soil types, the highest contents of organic carbon in different fractions were observed in plateau land, forest and farm lands, and black loessial soils, while the lowest contents of them were observed in gully bottom, grass land, and rubified soils, respectively. The relationships between organic carbon and environmental factors indicate that environmental factors not only directly influence the distribution of soil organic carbon, but also indirectly influence them through affecting the relationships among organic carbon fractions. The relationship between total organic carbon and labile organic carbon responses rapidly to environmental factors, while that between middle labile organic carbon and high labile organic carbon responses slowly to environmental factors. PMID:19143389

  7. Gravimetric Determination of Calcium as Calcium Carbonate Hydrate.

    ERIC Educational Resources Information Center

    Henrickson, Charles H.; Robinson, Paul R.

    1979-01-01

    The gravimetric determination of calcium as calcium carbonate is described. This experiment is suitable for undergraduate quantitative analysis laboratories. It is less expensive than determination of chloride as silver chloride. (BB)

  8. COMPARISON OF METHODS FOR DETERMINATION OF DISSOLVED INORGANIC CARBON

    EPA Science Inventory

    The presentation reviews several approaches for determining dissolved inorganic carbon (DIC) in drinking water. xperimental studies compared the accuracy and precision of DIC determination obtained by either direct analysis using a coulometric titration technique, or by comutatio...

  9. Organic carbon concentration profiles in recent cave sediments: records of agricultural pollution or diagenesis?

    PubMed

    Bottrell, S H

    1996-01-01

    Recent (<7 years old) cave sediments in Speedwell Cavern, Derbyshire, show an approximately exponential decay of organic carbon with depth. This phenomenon was thought to be due to one of two causes: (i) changing agricultural practice within the catchment feeding the cave, especially the increased use of sewage sludge and animal slurry as fertilizer; (ii) a relatively constant organic carbon concentration over time in the input sediment, with subsequent carbon mineralization during diagenesis. Carbon isotope composition of the organic material and the evolution of H/C ratio with depth indicate that the latter hypothesis is correct and that the profiles result from microbial diagenesis, not increased organic carbon inputs. By comparison with sediment of known (7 years) age, temporal decay constants for organic matter can be derived; these lie between rates previously determined for organic matter decomposition in marine sediments and soils. The H/C ratio of organic matter can be modelled as a function of time and proceeds in a similar fashion to soil organic material. PMID:15091425

  10. COSOLVENT EFFECTS ON ORGANIC CHEMICAL PARTITIONING TO SEDIMENT ORGANIC CARBON

    EPA Science Inventory

    Sorption-desorption hysteresis, slow desorption kinetics and resultant bioavailability, and other nonideal phenomena have been attributed to the differing sorptive characteristics of the natural organic polymers associated with soils and sediments. The objectives of this study we...

  11. The characterization and bioavailability of dissolved organic carbon in deep subsurface and surface waters

    SciTech Connect

    Palumbo, A.V.; Jardine, P.M.; McCarthy, J.F. ); Zaidi, B.R. . Dept. of Marine Sciences)

    1990-01-01

    We characterized and compared the bioavailability of chemical fractions of dissolved organic carbon (DOC) from deep wells at the US Department of Energy Savannah River Plant (SRP) site with that from South Carolina surface waters. Experiments with three bacterial cultures (Corynebacterium sp., Pseudomonas sp., and a bacteria included isolated from the surface water) indicated that the bioavailability of the carbon in the near surface water may be limited by inorganic nutrients. Associated with well-defined organic compounds. The purpose of this preliminary investigation was to improve our understanding of the organic matter in groundwater by characterizing the natural organic matter in water recovered from different formations in the Deep Probe Subsurface Microbiology program and by determining if the natural organic carbon can support growth of bacterial populations. The characterization was directed at elucidating the properties of of dissolved or colloidal organic matter that are relevant to the transport and mobility of the organic matter (and contaminants sorbed to the organic matter) and that may also be relevant to the potential role of organic matter in groundwater as a nutrient source supporting microbial productivity in the deep subsurface. A secondary objective of this study was to determine the factors limiting microbial growth in surface waters and near surface groundwaters and to determine the response of the microbial community to a mixing of these waters.

  12. Soil organic carbon mining versus priming - controls of soil organic carbon stocks along a management gradient

    NASA Astrophysics Data System (ADS)

    Blanes, M. Carmen; Reinsch, Sabine; Glanville, Helen C.; Jones, Davey L.; Carreira, José A.; Pastrana, David N.; Emmett, Bridget A.

    2015-04-01

    Soil carbon (C), nitrogen (N) and phosphorous (P) are assumed to be connected stoichiometrically and C:N(:P) ratios are frequently used to interpret the soils nutrient status. However, plants are capable of initiating the supply of nutrients by releasing rhizodeposits into the soil, thereby stimulating soil organic matter decomposition mediated by the rhizosphere microbial community. To test the relative importance of the two mechanisms across a fertility gradient in the UK we carried out a laboratory experiment. Intact soil cores from two depths (0-15 cm and 85-100 cm) were incubated and C, N and P were added in all possible combinations resulting in a total of 216 soil cores. Soil respiration was measured (1 h incubation, 10 oC) nine times over a 2 week period. Preliminary results indicate that all soils were C limited at the surface as measured as increased soil CO2 efflux. N additions increased soil respiration only marginally, whereas C+N stimulated microbial activity on the surface, and was even more pronounced in the deeper soil layer. Belowground responses to C+P were small and even smaller for N+P but similar for both soil depths. Our results indicate nutrient controls on soil organic matter turnover differ not only across a management/fertility gradient but also vertically down the soil profile.

  13. Organic farming enhances soil carbon and its benefits

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Increasing soil carbon through systematic agricultural practices provides an array of societal and farmer/producer benefits. Organic methods have been utilized for over 6000 years to conserve soil, water, energy, and biological resources. Many of the benefits of organic technologies identified in ...

  14. Microbial Contribution to Organic Carbon Sequestration in Mineral Soil

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soil productivity and sustainability are dependent on soil organic matter (SOM). Our understanding on how organic inputs to soil from microbial processes become converted to SOM is still limited. This study aims to understand how microbes affect carbon (C) sequestration and the formation of recalcit...

  15. Assessment of the potential of urban organic carbon dynamics to off-set urban anthropogenic emissions

    NASA Astrophysics Data System (ADS)

    Gottschalk, P.; Churkina, G.; Wattenbach, M.; Cubasch, U.

    2010-12-01

    The impact of urban systems on current and future global carbon emissions has been a focus of several studies. Many mitigation options in terms of increasing energy efficiency are discussed. However, apart from technical mitigation potential urban systems also have a considerable biogenic potential to mitigate carbon through an optimized management of organic carbon pools of vegetation and soil. Berlin city area comprises almost 50% of areas covered with vegetation or largely covered with vegetation. This potentially offers various areas for carbon mitigation actions. To assess the mitigation potentials our first objective is to estimate how large current vegetation and soil carbon stocks of Berlin are. We use publicly available forest and soil inventories to calculate soil organic carbon of non-pervious areas and forest standing biomass carbon. This research highlights data-gaps and assigns uncertainty ranges to estimated carbon resources. The second objective is to assess the carbon mitigation potential of Berlin’s vegetation and soils using a biogeochemical simulation model. BIOME-BGC simulates carbon-, nitrogen- and water-fluxes of ecosystems mechanistically. First, its applicability for Berlin forests is tested at selected sites. A spatial application gives an estimate of current net carbon fluxes. The application of such a model allows determining the sensitivity of key ecosystem processes (e.g. carbon gains through photosynthesis, carbon losses through decomposition) towards external drivers. This information can then be used to optimise forest management in terms of carbon mitigation. Initial results of Berlin’s current carbon stocks and its spatial distribution and preliminary simulations results will be presented.

  16. [The organic carbon--issues of hygienic regulation and harmonization].

    PubMed

    Kuz'mina, E A; Kuznetsov, E O; Smagina, N V; Slyshkina, T V; Akramov, R L; Brusnitsina, L A; Nitsak, G B; Nikonova, S V

    2013-01-01

    This study is devoted to the investigation of possibility to use the total organic carbon as regulated index in drinking water as well as to the issues of hygienic regulation and harmonizing this index with the standards of other countries. Basing on the results of 3 years lasting investigation carried out by Municipal Unitary Enterprise "Vodokanal" of Yekaterinburg city permits to propose as the most informative and reliable index of the presence of organic substances in drinking water the content of total organic carbon in comparison with currently regulated permanganate oxidability, chemical and biochemical oxygen consumption. PMID:24624824

  17. Assimilation of aged organic carbon in a glacial river food web

    NASA Astrophysics Data System (ADS)

    Fellman, J.; Hood, E. W.; Raymond, P. A.; Bozeman, M.; Hudson, J.; Arimitsu, M.

    2013-12-01

    Identifying the key sources of organic carbon supporting fish and invertebrate consumers is fundamental to our understanding of stream ecosystems. Recent laboratory bioassays highlight that aged organic carbon from glacier environments is highly bioavailable to stream bacteria relative to carbon originating from ice-free areas. However, there is little evidence suggesting that this aged, bioavailable organic carbon is also a key basal carbon source for stream metazoa. We used natural abundance of Δ14C, δ13C, and δ15N to determine if fish and invertebrate consumers are subsidized by aged organic carbon in a glacial river in southeast Alaska. We collected biofilm, leaf litter, three different species of macroinvertebrates, and resident juvenile salmonids from a reference stream and two sites (one site is directly downstream of the glacial outflow and one site is upstream of the tidal estuary) on the heavily glaciated Herbert River. Key producers, fish, and invertebrate consumers in the reference stream had carbon isotope values that ranged from -26 to -30‰ for δ13C and from -12 to 53‰ for Δ14C, reflecting a food web sustained mainly on contemporary primary production. In contrast, biofilm in the two glacial sites was highly Δ14C depleted (-203 to -215‰) relative to the reference site. Although biofilm may consist of both bacteria and benthic algae utilizing carbon depleted in Δ14C, δ13C values for biofilm (-24.1‰), dissolved inorganic carbon (-5.9‰), and dissolved organic carbon (-24.0‰) suggest that biofilm consist of bacteria sustained in part by glacier-derived, aged organic carbon. Invertebrate consumers (mean Δ14C of -80.5, mean δ13C of -26.5) and fish (mean Δ14C of -63.3, mean δ13C of -25.7) in the two glacial sites had carbon isotope values similar to biofilm. These results similarly show that aged organic carbon is incorporated into the metazoan food web. Overall, our findings indicate that continued watershed deglaciation and

  18. Aggregate and soil organic carbon dynamics in South Chilean Andisols

    NASA Astrophysics Data System (ADS)

    Huygens, D.; Boeckx, P.; Van Cleemput, O.; Oyarzún, C.; Godoy, R.

    2005-06-01

    Extreme sensitivity of soil organic carbon (SOC) to climate and land use change warrants further research in different terrestrial ecosystems. The aim of this study was to investigate the link between aggregate and SOC dynamics in a chronosequence of three different land uses of a south Chilean Andisol: a second growth Nothofagus obliqua forest (SGFOR), a grassland (GRASS) and a Pinus radiata plantation (PINUS). Total carbon content of the 0-10cm soil layer was higher for GRASS (6.7 kg C m-2) than for PINUS (4.3 kg C m-2, while TC content of SGFOR (5.8 kg C m-2) was not significantly different from either one. High extractable oxalate and pyrophosphate Al concentrations (varying from 20.3-24.4 g kg-1, and 3.9-11.1 g kg-1, respectively) were found in all sites. In this study, SOC and aggregate dynamics were studied using size and density fractionation experiments of the SOC, δ13C and total carbon analysis of the different SOC fractions, and C mineralization experiments. The results showed that electrostatic sorption between and among amorphous Al components and clay minerals is mainly responsible for the formation of metal-humus-clay complexes and the stabilization of soil aggregates. The process of ligand exchange between SOC and Al would be of minor importance resulting in the absence of aggregate hierarchy in this soil type. Whole soil C mineralization rate constants were highest for SGFOR and PINUS, followed by GRASS (respectively 0.495, 0.266 and 0.196 g CO2-Cm-2d-1 for the top soil layer). In contrast, incubation experiments of isolated macro organic matter fractions gave opposite results, showing that the recalcitrance of the SOC decreased in another order: PINUS>SGFOR>GRASS. We deduced that electrostatic sorption processes and physical protection of SOC in soil aggregates were the main processes determining SOC stabilization. As a result, high aggregate carbon concentrations, varying from 148 till 48 g kg-1, were encountered for all land use sites. Al

  19. Soil Organic Carbon Change Monitored Over Large Areas

    SciTech Connect

    Brown, David J.; Hunt, E. Raymond; Izaurralde, Roberto C.; Paustian, Keith H.; Rice, Charles W.; West, Tristram O.; Schumaker, Bonny L.

    2010-08-31

    Soils account for the largest fraction of terrestrial carbon (C); thus, they are critically important in determining global C cycle dynamics. In North America, conversion of native prairies to agricultural land use over 150 years ago released 30-50% of the soil organic carbon (SOC). Improved agricultural practices have the capacity to recover much of this SOC, storing it in biomass and soil and thereby removing billions of tons of atmospheric CO2. These practices involve increasing C inputs to soil (e.g., by crop rotations, increased use of higher biomass crops, perennial crops) and decreased losses (e.g., reduced tillage intensity) [Janzen et al., 1998; Lal et al., 2003; Smith et al., 2007]. Managing agricultural soils to increase SOC storage is a significant, immediately available, low-cost option for mitigating CO2 emissions, with a technical potential to offset as much as 800 Tg CO2/yr in the US (~13% of US CO2 emissions) [Lal et al., 2003] and 5000 Tg CO2/yr globally (~17% of global CO2 emissions) [Smith et al., 2007].

  20. Dissolved Organic Carbon in the Yukon River Basin

    NASA Astrophysics Data System (ADS)

    Aiken, G.; Striegl, R.; Schuster, P.

    2003-12-01

    A critical question in carbon cycling is how climate change could alter the fate and chemical nature of dissolved organic carbon (DOC) released from watersheds and transported to rivers, lakes, estuaries and coastal waters. The spatial and temporal variability of DOC in surface waters associated with the Yukon River Basin is being studied to better define the processes controlling DOC in this system. The Yukon River Basin, a large and diverse ecosystem in northwestern Canada and central Alaska, is experiencing increasing temperatures, partial melting of permafrost, drying of upland soils and changing wetland environments. However, little is known about DOC transported in the system. Specific ultraviolet absorbance (SUVA) measurements, in combination with DOC and DOC fractionation analyses, were used to determine both the amount and nature of DOC in the Yukon River and major tributaries. DOC transported in the Yukon River and its tributaries was seasonally dependent. For example, DOC concentrations in the Yukon River at Steven's Village ranged from 2 to 17 mg C/L during 2003, and SUVA ranged from 2.0 to 3.5 L/mg C m, indicating a large variation in amount and nature of organic matter in the river. Lowest DOC concentrations and SUVA values were observed in winter under low flow conditions. Greatest DOC concentrations were measured on samples collected during the spring on the leading part of the hydrograph. These samples were also found to have the greatest SUVA values indicating that the organic matter transported during this period was more aromatic than DOC transported under low flow conditions. High SUVA values are indicative of greater amounts of organic material originating in soils and wetlands of the watershed. The amount and nature of organic matter transported by the tributaries appeared to be related to relief and wetland contribution to the watershed of the tributary. Based on DOC and SUVA data, the Yukon River tributaries can be classified as dark water

  1. Maximum total organic carbon limit for DWPF melter feed

    SciTech Connect

    Choi, A.S.

    1995-03-13

    DWPF recently decided to control the potential flammability of melter off-gas by limiting the total carbon content in the melter feed and maintaining adequate conditions for combustion in the melter plenum. With this new strategy, all the LFL analyzers and associated interlocks and alarms were removed from both the primary and backup melter off-gas systems. Subsequently, D. Iverson of DWPF- T{ampersand}E requested that SRTC determine the maximum allowable total organic carbon (TOC) content in the melter feed which can be implemented as part of the Process Requirements for melter feed preparation (PR-S04). The maximum TOC limit thus determined in this study was about 24,000 ppm on an aqueous slurry basis. At the TOC levels below this, the peak concentration of combustible components in the quenched off-gas will not exceed 60 percent of the LFL during off-gas surges of magnitudes up to three times nominal, provided that the melter plenum temperature and the air purge rate to the BUFC are monitored and controlled above 650 degrees C and 220 lb/hr, respectively. Appropriate interlocks should discontinue the feeding when one or both of these conditions are not met. Both the magnitude and duration of an off-gas surge have a major impact on the maximum TOC limit, since they directly affect the melter plenum temperature and combustion. Although the data obtained during recent DWPF melter startup tests showed that the peak magnitude of a surge can be greater than three times nominal, the observed duration was considerably shorter, on the order of several seconds. The long surge duration assumed in this study has a greater impact on the plenum temperature than the peak magnitude, thus making the maximum TOC estimate conservative. Two models were used to make the necessary calculations to determine the TOC limit.

  2. Degradation of terrigenous dissolved organic carbon in the western Arctic Ocean.

    PubMed

    Hansell, Dennis A; Kadko, David; Bates, Nicholas R

    2004-05-01

    The largest flux of terrigenous organic carbon into the ocean occurs in dissolved form by way of rivers. The fate of this material is enigmatic; there are numerous reports of conservative behavior over continental shelves, but the only knowledge we have about removal is that it occurs on long unknown time scales in the deep ocean. To investigate the removal process, we evaluated terrigenous dissolved organic carbon concentration gradients in the Beaufort Gyre of the western Arctic Ocean, which allowed us to observe the carbon's slow degradation. Using isotopic tracers of water-mass age, we determined that terrigenous dissolved organic carbon is mineralized with a half-life of 7.1 +/- 3.0 years, thus allowing only 21 to 32% of it to be exported to the North Atlantic Ocean. PMID:15131302

  3. Substrate and environmental controls on microbial assimilation of soil organic carbon: a framework for Earth System Models

    SciTech Connect

    Xu, Xiaofeng; Schimel, Joshua; Thornton, Peter E; Song, Xia; Yuan, Fengming; Goswami, Santonu

    2014-01-01

    Microbial assimilation of soil organic carbon is one of the fundamental processes of global carbon cycling and it determines the magnitude of microbial biomass in soils. Mechanistic understanding of microbial assimilation of soil organic carbon and its controls is important for to improve Earth system models ability to simulate carbon-climate feedbacks. Although microbial assimilation of soil organic carbon is broadly considered to be an important parameter, it really comprises two separate physiological processes: one-time assimilation efficiency and time-dependent microbial maintenance energy. Representing of these two mechanisms is crucial to more accurately simulate carbon cycling in soils. In this study, a simple modeling framework was developed to evaluate the substrate and environmental controls on microbial assimilation of soil organic carbon using a new term: microbial annual active period (the length of microbes remaining active in one year). Substrate quality has a positive effect on microbial assimilation of soil organic carbon: higher substrate quality (lower C:N ratio) leads to higher ratio of microbial carbon to soil organic carbon and vice versa. Increases in microbial annual active period from zero stimulate microbial assimilation of soil organic carbon; however, when microbial annual active period is longer than an optimal threshold, increasing this period decreases microbial biomass. The simulated ratios of soil microbial biomass to soil organic carbon are reasonably consistent with a recently compiled global dataset at the biome-level. The modeling framework of microbial assimilation of soil organic carbon and its controls developed in this study offers an applicable ways to incorporate microbial contributions to the carbon cycling into Earth system models for simulating carbon-climate feedbacks and to explain global patterns of microbial biomass.

  4. Total organic carbon in aggregates as a soil recovery indicator

    NASA Astrophysics Data System (ADS)

    Luciene Maltoni, Katia; Rodrigues Cassiolato, Ana Maria; Amorim Faria, Glaucia; Dubbin, William

    2015-04-01

    The soil aggregation promotes physical protection of organic matter, preservation of which is crucial to improve soil structure, fertility and ensure the agro-ecosystems sustainability. The no-tillage cultivation system has been considered as one of the strategies to increase total soil organic carbono (TOC) contents and soil aggregation, both are closely related and influenced by soil management systems. The aim of this study was to evaluate the distribution of soil aggregates and the total organic carbon inside aggregates, with regard to soil recovery, under 3 different soil management systems, i.e. 10 and 20 years of no-tillage cultivation as compared with soil under natural vegetation (Cerrado). Undisturbed soils (0-5; 5-10; and 10-20 cm depth) were collected from Brazil, Central Region. The soils, Oxisols from Cerrado, were collected from a field under Natural Vegetation-Cerrado (NV), and from fields that were under conventional tillage since 1970s, and 10 and 20 years ago were changed to no-tillage cultivation system (NT-10; NT-20 respectively). The undisturbed samples were sieved (4mm) and the aggregates retained were further fractionated by wet sieving through five sieves (2000, 1000, 500, 250, and 50 μm) with the aggregates distribution expressed as percentage retained by each sieve. The TOC was determined, for each aggregate size, by combustion (Thermo-Finnigan). A predominance of aggregates >2000 μm was observed under NV treatment (92, 91, 82 %), NT-10 (64, 73, 61 %), and NT-20 (71, 79, 63 %) for all three depths (0-5; 5-10; 10-20 cm). In addition greater quantities of aggregates in sizes 1000, 500, 250 and 50 μm under NT-10 and NT-20 treatments, explain the lower aggregate stability under these treatments compared to the soil under NV. The organic C concentration for NV in aggregates >2000 μm was 24,4; 14,2; 8,7 mg/g for each depth (0-5; 5-10; 10-20 cm, respectively), higher than in aggregates sized 250-50 μm (7,2; 5,5; 4,4 mg/g) for all depths

  5. Linking aboveground net primary productivity to soil carbon and dissolved organic carbon in complex terrain

    NASA Astrophysics Data System (ADS)

    Peterson, Fox S.; Lajtha, Kate J.

    2013-07-01

    Factors influencing soil organic matter (SOM) stabilization and dissolved organic carbon (DOC) content in complex terrain, where vegetation, climate, and topography vary over the scale of a few meters, are not well understood. We examined the spatial correlations of lidar and geographic information system-derived landscape topography, empirically measured soil characteristics, and current and historical vegetation composition and structure versus SOM fractions and DOC pools and leaching on a small catchment (WS1) in the H.J. Andrews Experimental Forest, located in the western Cascades Range of Oregon, USA. We predicted that aboveground net primary productivity (ANPP), litter fall, and nitrogen mineralization would be positively correlated with SOM, DOC, and carbon (C) content of the soil based on the principle that increased C inputs cause C stores in and losses from in the soil. We expected that in tandem, certain microtopographical and microclimatic characteristics might be associated with elevated C inputs and correspondingly, soil C stores and losses. We confirmed that on this site, positive relationships exist between ANPP, C inputs (litter fall), and losses (exportable DOC), but we did not find that these relationships between ANPP, inputs, and exports were translated to SOM stores (mg C/g soil), C content of the soil (% C/g soil), or DOC pools (determined with salt and water extractions). We suggest that the biogeochemical processes controlling C storage and lability in soil may relate to longer-term variability in aboveground inputs that result from a heterogeneous and evolving forest stand.

  6. Sedimentation of particulate organic carbon on the Amundsen Shelf, Antarctica

    NASA Astrophysics Data System (ADS)

    Kim, Minkyoung; Hwang, Jeomshik; Lee, Sang H.; Kim, Hyung J.; Kim, Dongseon; Yang, Eun J.; Lee, SangHoon

    2016-01-01

    We examined the recent history of sedimentary organic carbon (SOC) accumulation on the western Amundsen Shelf, to help characterize the biological carbon pump in the Amundsen Sea, Antarctica. Vertical sedimentary profiles (in the upper 21-cm) of SOC content, radio- and stable-carbon isotopes were obtained at four locations in the western Amundsen Sea: near the shelf break, inside the polynya near the Dotson Ice Shelf, and at both the periphery and the center of the Amundsen Sea polynya. Profiles were representative not only of various distances from the coast, but also of various summertime sea ice conditions and bottom depths. The SOC content (up to 1.1%) and the radiocarbon content were distinctly higher at the periphery and at the center of the polynya than at the other sites. The SOC and 14C contents were generally consistent with the spatial distribution of primary productivity in the surface water. A linear SOC accumulation rate of about 1.0 g C m-2 yr-1 was determined from the conventional 14C ages of bulk SOC below the surface mixed layer at the periphery and at the center of the polynya, for the time period of 3.1-4.7 kyr before present (BP). This linear SOC accumulation rate was about 20 times greater than the rates determined at the two other sites for the period of 4.6-15.7 kyr BP. Note that all values are for uncorrected 14C ages. At the center of the polynya, a sudden change in SOC accumulation rate was observed at about 16 cm depth, corresponding to 4.7 kyr BP, implying that changes (during this time period) in physical environments greatly affected primary production, SOC burial and/or supply of allochthonous particles to this site. The vertical distribution of 14C content in the sediments implies that aged organic matter, likely associated with resuspended sediments, was also being deposited inside the polynya, in addition to autochthonous biogenic particles. If our estimation of SOC accumulation is extrapolated to the western Amundsen Shelf

  7. Molecular profiling of permafrost soil organic carbon composition and degradation

    NASA Astrophysics Data System (ADS)

    Gu, B.; Mann, B.

    2014-12-01

    Microbial degradation of soil organic matter (SOM) is a key process for terrestrial carbon (C) cycling, though the dynamics of these transformations remain unclear at the molecular level. This study reports the application of ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) to profile molecular components of Arctic SOM collected from the surface water and the mineral horizon of a low-centered polygon soil at Barrow Environmental Observatory (BEO), Barrow, Alaska. Soil samples were subjected to anaerobic warming experiments for a period of 40 days, and the SOM was extracted before and after the incubation to determine the components of organic C that were degraded over the course of the study. A CHO index based on molecular composition data was utilized to codify SOM components according to their observed degradation potential. Carbohydrate- and lignin-like compounds in the water-soluble fraction (WSF) demonstrated a high degradation potential, while structures with similar stoichiometries in the base-soluble fraction (BSF) were not readily degraded. The WSF of SOM also shifted to a wider range of measured molecular masses including an increased prevalence of larger compounds, while the size distribution of compounds in the BSF changed little over the same period. Additionally, the molecular profiling data indicated an apparently ordered incorporation of organic nitrogen in the BSF immobilized as primary and secondary amines, possibly as components of N-heterocycles, which may provide insight into nitrogen immobilization or mobilization processes in SOM. Our study represents an important step forward for studying Arctic SOM with improved understanding of the molecular properties of soil organic C and the ability to represent SOM in climate models that will predict the impact of climate change on soil C and nutrient cycling.

  8. Dissolved organic carbon losses from tile drained agroecosystems.

    PubMed

    Ruark, Matthew D; Brouder, Sylvie M; Turco, Ronald F

    2009-01-01

    Artificial subsurface drainage is commonly used in midwestern agriculture and drainage losses of dissolved organic carbon (DOC) from such systems are an under-quantified portion of the terrestrial carbon (C) cycle. The objectives of this study were to determine the effect of common agricultural management practices on DOC losses from subsurface tile drains and to assess patterns of loss as a function of year, time of year, and drainflow. Daily drainflow was collected across six water years (1999-2004) from a restored prairie grass system and cropping systems which include continuous corn (Zea mays L.) and corn-soybean [Glycine max (L.) Merr.] rotations fertilized with urea-ammonium-nitrate (UAN) or swine (Sus scrofa) manure lagoon effluent. The DOC concentrations in tile drainflow were low, typically <2 mg L(-1). Yearly DOC losses, which ranged from 1.78 to 8.61 kg ha(-1), were not affected by management practices and were small compared to organic C inputs. Spring application of lagoon effluent increased yearly flow-weighted (FW)-DOC concentrations relative to other cropping systems in three of the years and increased monthly FW-DOC concentrations when drainflow occurred within 1 mo of application. Drainflow was significantly and positively correlated with DOC loss. Drainflow also affected DOC concentrations as greater 6-yr cumulative drainflow was associated with lower 6-yr FW-DOC concentrations and greater daily drainflow was associated with higher daily DOC concentrations. Our results indicate that lagoon effluent application and fertilizer N rates do not affect long-term losses of DOC from tile drains and that drainflow is the main driver of DOC losses. PMID:19398518

  9. Organic carbon leaching behavior from incinerator bottom ash.

    PubMed

    Guimaraes, A L; Okuda, T; Nishijima, W; Okada, M

    2006-09-21

    The understanding of the leaching behavior of organic carbon from incinerator bottom ash is an important aspect for the control of organic carbon emissions from landfills in order to minimize their potential risk to the environment. The leaching behavior of organic carbon from incinerator bottom ash samples, obtained from two different solid waste sources, as well as the effects of calcium (Ca) on organic carbon (DOC) leaching associated with pH were therefore investigated in this paper. The effect of pH on the leaching of DOC and other major elements from bottom ash was ascertained through pH-stat leaching experiments. Column leaching experiments were carried out to evaluate the dependence of the leached amount of DOC on Ca leaching. It was found that the bottom ash produced by incineration of municipal solid waste (MSW) was composed of two DOC fractions: DOC leached independent (fraction I) of Ca leaching, observed at alkaline-neutral pH, and DOC leached dependent (fraction II) on Ca leaching, observed at acid pH. However, the bottom ash produced by incineration of industrial solid waste (ISW) was composed of only DOC fraction I. The addition of calcium oxide during incineration and the differences in the paper to plastic ratio in the physical composition of the solid wastes incinerated would explain the distinct organic carbon leaching behaviors of bottom ash samples. PMID:16675109

  10. Potential Influence of Perchlorate on Organic Carbon in Martian Regolith

    NASA Astrophysics Data System (ADS)

    Oze, C.; Vithanage, M. S.; Kumarathilaka, P. R.; Indraratne, S.; Horton, T. W.

    2014-12-01

    Perchlorate is a strong oxidizer present at elevated concentrations in surface martian regolith. Chemical and isotopic modification of potential organic carbon with perchlorate in martian regolith during H2O(l) interactions is unknown. Here we assess the relationship between martian levels of perchlorate and organic carbon present in life harbouring geologic material from Earth. These materials represent chemical (i.e., processed serpentine soils from Sri Lanka) and temperature (i.e., hydrothermal jarosite/goethite deposit from White Island, New Zealand) extremes to where life exists on Earth. Preliminary evidence demonstrates that organic carbon decreases and δ13C values are modified for ultramafic sediment in both perchlorate kinetic and incubation experiments. In hydrothermal jarosite/goethite with microbial communities present, total and organic carbon is maintained and little modification in δ13C values is apparent. These preliminary results suggest that surface hydrothermal deposits with mineralogically 'protected' organic carbon are preferable sites to assess the potential of life on Mars.

  11. Organics on Titan : Carbon Rings and Carbon Cycles (Invited)

    NASA Astrophysics Data System (ADS)

    Lorenz, R. D.

    2010-12-01

    The photochemical conversion of methane into heavier organics which would cover Titan’s surface has been a principal motif of Titan science for the last 4 decades. Broadly, this picture has held up against Cassini observations, but organics on Titan turn out to have some surprising characteristics. First, the surface deposits of organics are segregated into at least two distinct major reservoirs - equatorial dune sands and polar seas. Second, the rich array of compounds detected as ions and molecules even 1000km above Titan’s surface has proven much more complex than expected, including two-ring anthracene and compounds with m/z>1000. Radar and near-IR mapping shows that Titan’s vast dunefields, covering >10% of Titan’s surface, contain ~0.3 million km^3 of material. This material is optically dark and has a low dielectric constant, consistent with organic particulates. Furthermore, the dunes are associated with a near-IR spectral signature attributed to aromatic compounds such as benzene, which has been sampled in surprising abundance in Titan’s upper atmosphere. The polar seas and lakes of ethane (and presumably at least some methane) may have a rather lower total volume than the dune sands, and indeed may contain little more, if any, methane than the atmosphere itself. The striking preponderance of liquid deposits in the north, notably the 500- and 1000-km Ligeia and Kraken, contrasts with the apparently shallow and shrinking Ontario Lacus in the south, and perhaps attests to volatile migration on astronomical (Croll-Milankovich) timescales as well as seasonal methane transport. Against this appealing picture, many questions remain. What is the detailed composition of the seas, and can chemistry in a nonpolar solvent yield compounds of astrobiological interest ? Are there ‘groundwater’ reservoirs of methane seething beneath the surface, perhaps venting to form otherwise improbable equatorial clouds? And what role, if any, do clathrates play today

  12. Stream bed organic carbon and biotic integrity.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Allochthonous organic matter provides a basis for some stream ecosystems. Channel incision, which is a common result of anthropogenic impacts on watersheds and stream channels, may deplete stream bed C stores due to erosion, less frequent hydrologic exchanges between stream and floodplain, and remov...

  13. Soil organic carbon sequestration with conservation management

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The southeastern USA has approximately 111 million acres (45 Mha) in agricultural production. This extensive land resource has the potential to sequester soil organic C (SOC), especially following historical conversion of land, first from native forest to intensively cultivated cropland and more re...

  14. Evaluation of estimation methods for organic carbon normalized sorption coefficients

    USGS Publications Warehouse

    Baker, James R.; Mihelcic, James R.; Luehrs, Dean C.; Hickey, James P.

    1997-01-01

    A critically evaluated set of 94 soil water partition coefficients normalized to soil organic carbon content (Koc) is presented for 11 classes of organic chemicals. This data set is used to develop and evaluate Koc estimation methods using three different descriptors. The three types of descriptors used in predicting Koc were octanol/water partition coefficient (Kow), molecular connectivity (mXt) and linear solvation energy relationships (LSERs). The best results were obtained estimating Koc from Kow, though a slight improvement in the correlation coefficient was obtained by using a two-parameter regression with Kow and the third order difference term from mXt. Molecular connectivity correlations seemed to be best suited for use with specific chemical classes. The LSER provided a better fit than mXt but not as good as the correlation with Koc. The correlation to predict Koc from Kow was developed for 72 chemicals; log Koc = 0.903* log Kow + 0.094. This correlation accounts for 91% of the variability in the data for chemicals with log Kow ranging from 1.7 to 7.0. The expression to determine the 95% confidence interval on the estimated Koc is provided along with an example for two chemicals of different hydrophobicity showing the confidence interval of the retardation factor determined from the estimated Koc. The data showed that Koc is not likely to be applicable for chemicals with log Kow < 1.7. Finally, the Koc correlation developed using Kow as a descriptor was compared with three nonclass-specific correlations and two 'commonly used' class-specific correlations to determine which method(s) are most suitable.

  15. Influence of carbonization methods on the aromaticity of pyrogenic dissolved organic carbon

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Dissolved organic carbon (DOC) components of soil amendments such as biochar will influence the fundamental soil chemistry including the metal speciation, nutrient availability, and microbial activity. Quantitative correlation is necessary between (i) pyrogenic DOC components of varying aromaticity...

  16. One carbon metabolism in anaerobic bacteria: Regulation of carbon and electron flow during organic acid production

    SciTech Connect

    Zeikus, J.G.; Jain, M.

    1993-12-31

    The project deals with understanding the fundamental biochemical mechanisms that physiologically control and regulate carbon and electron flow in anaerobic chemosynthetic bacteria that couple metabolism of single carbon compounds and hydrogen to the production of organic acids (formic, acetic, butyric, and succinic) or methane. The authors compare the regulation of carbon dioxide and hydrogen metabolism by fermentation, enzyme, and electron carrier analysis using Butyribacterium methylotrophicum, Anaeroblospirillum succiniciproducens, Methanosarcina barkeri, and a newly isolated tri-culture composed of a syntrophic butyrate degrader strain IB, Methanosarcina mazei and Methanobacterium formicicum as model systems. To understand the regulation of hydrogen metabolism during butyrate production or acetate degradation, hydrogenase activity in B. methylotrophicum or M. barkeri is measured in relation to growth substrate and pH; hydrogenase is purified and characterized to investigate number of hydrogenases; their localization and functions; and, their sequences are determined. To understand the mechanism for catabolic CO{sub 2} fixation to succinate the PEP carboxykinase enzyme and gene of A. succiniciproducens are purified and characterized. Genetically engineered strains of Escherichia coli containing the phosphoenolpyruvate (PEP) carboxykinase gene are examined for their ability to produce succinate in high yield. To understand the mechanism of fatty acid degradation by syntrophic acetogens during mixed culture methanogenesis formate and hydrogen production are characterized by radio tracer studies. It is intended that these studies provide strategies to improve anaerobic fermentations used for the production of organic acids or methane and, new basic understanding on catabolic CO{sub 2} fixation mechanisms and on the function of hydrogenase in anaerobic bacteria.

  17. A Raman Study of Carbonates and Organic Contents in Five CM Chondrites

    NASA Technical Reports Server (NTRS)

    Chan, Q. H. S.; Zolensky, M. E.; Bodnar, R. J.; Farley, C.; Cheung, J. C. H.

    2016-01-01

    Carbonates comprise the second most abundant class of carbon-bearing phases in carbonaceous chondrites after organic matter (approximately 2 wt.%), followed by other C-bearing phases such as diamond, silicon carbide, and graphite. Therefore, understanding the abundances of carbonates and the associated organic matter provide critical insight into the genesis of major carbonaceous components in chondritic materials. Carbonates in CM chondrites mostly occur as calcite (of varying composition) and dolomite. Properly performed, Raman spectroscopy provides a non-destructive technique for characterizing meteorite mineralogy and organic chemistry. It is sensitive to many carbonaceous phases, allows the differentiation of organic from inorganic materials, and the interpretation of their spatial distribution. Here, with the use of Raman spectroscopy, we determine the structure of the insoluble organic matter (IOM) in the matrix and carbonate phases in five CM chondrites: Jbilet Winselwan, Murchison, Nogoya, Santa Cruz, and Wisconsin Range (WIS) 91600, and interpret the relative timing of carbonate precipitation and the extent of the associated alteration events.

  18. Chemistry of organic carbon in soil with relationship to the global carbon cycle

    SciTech Connect

    Post, W.M. III

    1988-01-01

    Various ecosystem disturbances alter the balances between production of organic matter and its decomposition and therefore change the amount of carbon in soil. The most severe perturbation is conversion of natural vegetation to cultivated crops. Conversion of natural vegetation to cultivated crops results in a lowered input of slowly decomposing material which causes a reduction in overall carbon levels. Disruption of soil matrix structure by cultivation leads to lowered physical protection of organic matter resulting in an increased net mineralization rate of soil carbon. Climate change is another perturbation that affects the amount and composition of plant production, litter inputs, and decomposition regimes but does not affect soil structure directly. Nevertheless, large changes in soil carbon storage are probable with anticipated CO2 induced climate change, particularly in northern latitudes where anticipated climate change will be greatest (MacCracken and Luther 1985) and large amounts of soil organic matter are found. It is impossible, given the current state of knowledge of soil organic matter processes and transformations to develop detailed process models of soil carbon dynamics. Largely phenomenological models appear to be developing into predictive tools for understanding the role of soil organic matter in the global carbon cycle. In particular, these models will be useful in quantifying soil carbon changes due to human land-use and to anticipated global climate and vegetation changes. 47 refs., 7 figs., 2 tabs.

  19. Maximum organic carbon limits at different melter feed rates (U)

    SciTech Connect

    Choi, A.S.

    1995-12-31

    This report documents the results of a study to assess the impact of varying melter feed rates on the maximum total organic carbon (TOC) limits allowable in the DWPF melter feed. Topics discussed include: carbon content; feed rate; feed composition; melter vapor space temperature; combustion and dilution air; off-gas surges; earlier work on maximum TOC; overview of models; and the results of the work completed.

  20. Charcoal bed operation for optimal organic carbon removal

    SciTech Connect

    Merritt, C.M.; Scala, F.R.

    1995-05-01

    Historically, evaporation, reverse osmosis or charcoal-demineralizer systems have been used to remove impurities in liquid radwaste processing systems. At Nine Mile point, we recently replaced our evaporators with charcoal-demineralizer systems to purify floor drain water. A comparison of the evaporator to the charcoal-demineralizer system has shown that the charcoal-demineralizer system is more effective in organic carbon removal. We also show the performance data of the Granulated Activated Charcoal (GAC) vessel as a mechanical filter. Actual data showing that frequent backflushing and controlled flow rates through the GAC vessel dramatically increases Total Organic Carbon (TOC) removal efficiency. GAC vessel dramatically increases Total Organic Carbon (TOC) removal efficiency. Recommendations are provided for operating the GAC vessel to ensure optimal performance.

  1. An electrochemically based total organic carbon analyzer for planetary and terrestrial on-site applications.

    PubMed

    Stroble, Shannon T; Kounaves, Samuel P

    2012-07-17

    The search for organics on Mars began over 30 years ago. Neither the Viking GC/MS nor the more recent thermal and evolved gas analyzer (TEGA) aboard Phoenix were successful in detecting organics in the Martian soil. The most recent hypothesis for the "missing" Martian organics is thermal decomposition of organic material to CO(2) during the pyrolysis step of these analyses caused by the recently discovered ~1 wt % perchlorate in the Martian soil. To avoid this problem, an entirely different approach for the analysis of organics on Mars has been developed using an electrochemically based total organic carbon (TOC) analyzer, designated the Mars Organic Carbon Analyzer (MOCA). MOCA is designed as a small, lightweight, low-power instrument that electrochemically oxidizes organics to CO(2). The CO(2) is subsequently detected and quantified to determine the amount of TOC in the soil. MOCA can use the perchlorate present in the Martian soil to its advantage as an electrolyte, thus requiring only a buffered solution. Through a series of proof-of-concept tests, MOCA is shown to oxidize a variety of low-molecular-weight 1-5-carbon-containing molecules, including those containing carbon-13 using platinum and boron-doped diamond (BDD) electrodes at concentrations as low as 10 mg/kg. MOCA can also be used in terrestrial settings for on-site analysis of dissolved TOC. PMID:22725848

  2. Soil Organic Carbon dynamics in agricultural soils of Veneto Region

    NASA Astrophysics Data System (ADS)

    Bampa, F. B.; Morari, F. M.; Hiederer, R. H.; Toth, G. T.; Giandon, P. G.; Vinci, I. V.; Montanarella, L. M.; Nocita, M.

    2012-04-01

    One of the eight soil threats expressed in the European Commission's Thematic Strategy for Soil Protection (COM (2006)231 final) it's the decline in Soil Organic Matter (SOM). His preservation is recognized as with the objective to ensure that the soils of Europe remain healthy and capable of supporting human activities and ecosystems. One of the key goals of the strategy is to maintain and improve Soil Organic Carbon (SOC) levels. As climate change is identified as a common element in many of the soil threats, the European Commission (EC) intends to assess the actual contribution of the soil protection to climate change mitigation and the effects of climate change on the possible depletion of SOM. A substantial proportion of European land is occupied by agriculture, and consequently plays a crucial role in maintaining natural resources. Organic carbon preservation and sequestration in the EU's agricultural soils could have some potential to mitigate the effects of climate change, particularly linked to preventing certain land use changes and maintaining SOC stocks. The objective of this study is to assess the SOC dynamics in agricultural soils (cropland and grassland) at regional scale, focusing on changes due to land use. A sub-objective would be the evaluation of the most used land management practices and their effect on SOC content. This assessment aims to determine the geographical distribution of the potential GHG mitigation options, focusing on hot spots in the EU, where mitigation actions would be particularly efficient and is linked with the on-going work in the JRC SOIL Action. The pilot area is Veneto Region. The data available are coming from different sources, timing and involve different variables as: soil texture, climate, soil disturbance, managements and nutrients. The first source of data is the LUCAS project (Land Use/Land Cover Area Frame statistical Survey). Started in 2001, the LUCAS project aims to monitor changes in land cover/use and

  3. Raman spectroscopy: Caution when interpreting organic carbon from oxidising environments

    NASA Astrophysics Data System (ADS)

    Brolly, Connor; Parnell, John; Bowden, Stephen

    2016-02-01

    Oxidation on Mars is primarily caused by the high influx of cosmic and solar radiation which interacts with the Martian surface. The evidence of this can be seen in the ubiquitous red colouration of the Martian sediment. This radiation will destroy most signals of life in the top few metres of the Martian surface. If organic carbon (one of the building blocks of life) is present within the accessible Martian sediments, it is very likely that it will have experienced some oxidation. ESA's ExoMars mission set to fly in 2018, has on board a miniaturised Raman spectrometer. As Raman spectroscopy is sensitive to carbonaceous material and will be primarily used to characterise organics, it is essential that the effect oxidation has on the Raman carbon signal is assessed. Oxidised carbonaceous shales were analysed using Raman spectroscopy to assess this issue. Results show that haematite has a band which occurs in the same frequency as the carbon D band, which cannot be distinguished from each other. This can lead to a misidentification of the carbon D band and a misinterpretation of the carbon order. Consequently, caution must be taken when applying Raman spectroscopy for organic carbon analysis in oxidised terrestrial and extraterrestrial environments, including on Mars.

  4. Fluvial organic carbon losses from a Bornean blackwater river

    NASA Astrophysics Data System (ADS)

    Moore, S.; Gauci, V.; Evans, C. D.; Page, S. E.

    2010-11-01

    The transport of carbon from terrestrial ecosystems such as peatlands into rivers and out to the oceans plays an important role in the carbon cycle because it provides a link between the terrestrial and marine carbon cycles. Concentrations of dissolved organic carbon (DOC) and particulate organic carbon (POC) were analysed from the source to the mouth of the River Sebangau in Central Kalimantan, Indonesia during the dry and wet seasons in 2008/2009 and an annual total organic carbon (TOC) flux estimated. DOC concentrations were higher and POC concentrations lower in the wet season compared to the dry season. As seen in other tropical blackwater rivers, DOC concentration is consistently around 10 times greater than POC concentration. We estimate the annual TOC flux discharged to the Java Sea to be 0.46 Tg year-1 comprising of 93% (0.43 Tg) DOC and 7% (0.03 Tg) POC. This equates to a fluvial TOC loss flux per unit area over the entire Sebangau catchment of 88 g C m-2 yr-1. When extrapolating this TOC loss flux to the peat covered area of Indonesia (206 950 km2), we estimate a TOC loss of 18.2 Tg C yr-1 or ~10% of current estimates of the global annual riverine DOC discharge into the ocean.

  5. Fluvial organic carbon losses from a Bornean blackwater river

    NASA Astrophysics Data System (ADS)

    Moore, S.; Gauci, V.; Page, S.; Evans, C.; Limin, S.

    2010-12-01

    The transport of carbon from terrestrial ecosystems such as peatlands into rivers and out to the oceans plays an important role in the carbon cycle because it provides a link between the terrestrial and marine carbon cycles. Concentrations of dissolved organic carbon (DOC) and particulate organic carbon (POC) were analysed from the source to the mouth of the River Sebangau in Central Kalimantan, Indonesia during the dry and wet seasons in 2008/2009 and an annual total organic carbon (TOC) flux estimated. DOC concentrations were higher and POC concentrations lower in the wet season compared to the dry season. As seen in other tropical blackwater rivers, DOC concentration is consistently around 10 times greater than POC concentration. We estimate the annual TOC flux discharged to the Java Sea to be 0.46 Tg year-1 comprising of 93% (0.43 Tg) DOC and 7% (0.03 Tg) POC. This equates to a fluvial TOC loss flux per unit area over the entire Sebangau catchment of 88g C m-2 yr-1. When extrapolating the Sebangau catchment TOC loss flux (88g C m-2 yr-1) to the peat covered area of Indonesia (206,950 km2), we calculate a TOC loss of 18.2 Tg C yr-1 or ~10% of current estimates of the global annual riverine DOC discharge into the ocean.

  6. Factors influencing organic carbon preservation in marine sediments

    NASA Technical Reports Server (NTRS)

    Canfield, D. E.

    1994-01-01

    The organic matter that escapes decomposition is buried and preserved in marine sediments, with much debate as to whether the amount depends on bottom-water O2 concentration. One group argues that decomposition is more efficient with O2, and hence, organic carbon will be preferentially oxidized in its presence, and preserved in its absence. Another group argues that the kinetics of organic matter decomposition are similar in the presence and absence of O2, and there should be no influence of O2 on preservation. A compilation of carbon preservation shows that both groups are right, depending on the circumstances of deposition. At high rates of deposition, such as near continental margins, little difference in preservation is found with varying bottom-water O2. It is important that most carbon in these sediments decomposes by anaerobic pathways regardless of bottom-water O2. Hence, little influence of bottom-water O2 on preservation would, in fact, be expected. As sedimentation rate drops, sediments deposited under oxygenated bottom water become progressively more aerobic, while euxinic sediments remain anaerobic. Under these circumstances, the relative efficiencies of aerobic and anaerobic decomposition could affect preservation. Indeed, enhanced preservation is observed in low-O2 and euxinic environments. To explore in detail the factors contributing to this enhanced carbon preservation, aspects of the biochemistries of the aerobic and anaerobic process are reviewed. Other potential influences on preservation are also explored. Finally, a new model for organic carbon decomposition, the "pseudo-G" model, is developed. This model couples the degradation of refractory organic matter to the overall metabolic activity of the sediment, and has consequences for carbon preservation due to the mixing together of labile and refractory organic matter by bioturbation.

  7. Pathways of organic carbon oxidation in three continental margin sediments

    NASA Technical Reports Server (NTRS)

    Canfield, D. E.; Jorgensen, B. B.; Fossing, H.; Glud, R.; Gundersen, J.; Ramsing, N. B.; Thamdrup, B.; Hansen, J. W.; Nielsen, L. P.; Hall, P. O.

    1993-01-01

    We have combined several different methodologies to quantify rates of organic carbon mineralization by the various electron acceptors in sediments from the coast of Denmark and Norway. Rates of NH4+ and Sigma CO2 liberation sediment incubations were used with O2 penetration depths to conclude that O2 respiration accounted for only between 3.6-17.4% of the total organic carbon oxidation. Dentrification was limited to a narrow zone just below the depth of O2 penetration, and was not a major carbon oxidation pathway. The processes of Fe reduction, Mn reduction and sulfate reduction dominated organic carbon mineralization, but their relative significance varied depending on the sediment. Where high concentrations of Mn-oxide were found (3-4 wt% Mn), only Mn reduction occurred. With lower Mn oxide concentrations more typical of coastal sediments, Fe reduction and sulfate reduction were most important and of a similar magnitude. Overall, most of the measured O2 flux into the sediment was used to oxidized reduced inorganic species and not organic carbon. We suspect that the importance of O2 respiration in many coastal sediments has been overestimated, whereas metal oxide reduction (both Fe and Mn reduction) has probably been well underestimated.

  8. Erosion of organic carbon in the Arctic as a geological carbon dioxide sink

    NASA Astrophysics Data System (ADS)

    Hilton, Robert G.; Galy, Valier; Gaillardet, Jérôme; Dellinger, Mathieu; Bryant, Charlotte; O'Regan, Matt; Gröcke, Darren R.; Coxall, Helen; Bouchez, Julien; Calmels, Damien

    2015-08-01

    Soils of the northern high latitudes store carbon over millennial timescales (thousands of years) and contain approximately double the carbon stock of the atmosphere. Warming and associated permafrost thaw can expose soil organic carbon and result in mineralization and carbon dioxide (CO2) release. However, some of this soil organic carbon may be eroded and transferred to rivers. If it escapes degradation during river transport and is buried in marine sediments, then it can contribute to a longer-term (more than ten thousand years), geological CO2 sink. Despite this recognition, the erosional flux and fate of particulate organic carbon (POC) in large rivers at high latitudes remains poorly constrained. Here, we quantify the source of POC in the Mackenzie River, the main sediment supplier to the Arctic Ocean, and assess its flux and fate. We combine measurements of radiocarbon, stable carbon isotopes and element ratios to correct for rock-derived POC. Our samples reveal that the eroded biospheric POC has resided in the basin for millennia, with a mean radiocarbon age of 5,800 +/- 800 years, much older than the POC in large tropical rivers. From the measured biospheric POC content and variability in annual sediment yield, we calculate a biospheric POC flux of teragrams of carbon per year from the Mackenzie River, which is three times the CO2 drawdown by silicate weathering in this basin. Offshore, we find evidence for efficient terrestrial organic carbon burial over the Holocene period, suggesting that erosion of organic carbon-rich, high-latitude soils may result in an important geological CO2 sink.

  9. Erosion of organic carbon in the Arctic as a geological carbon dioxide sink.

    PubMed

    Hilton, Robert G; Galy, Valier; Gaillardet, Jérôme; Dellinger, Mathieu; Bryant, Charlotte; O'Regan, Matt; Gröcke, Darren R; Coxall, Helen; Bouchez, Julien; Calmels, Damien

    2015-08-01

    Soils of the northern high latitudes store carbon over millennial timescales (thousands of years) and contain approximately double the carbon stock of the atmosphere. Warming and associated permafrost thaw can expose soil organic carbon and result in mineralization and carbon dioxide (CO2) release. However, some of this soil organic carbon may be eroded and transferred to rivers. If it escapes degradation during river transport and is buried in marine sediments, then it can contribute to a longer-term (more than ten thousand years), geological CO2 sink. Despite this recognition, the erosional flux and fate of particulate organic carbon (POC) in large rivers at high latitudes remains poorly constrained. Here, we quantify the source of POC in the Mackenzie River, the main sediment supplier to the Arctic Ocean, and assess its flux and fate. We combine measurements of radiocarbon, stable carbon isotopes and element ratios to correct for rock-derived POC. Our samples reveal that the eroded biospheric POC has resided in the basin for millennia, with a mean radiocarbon age of 5,800 ± 800 years, much older than the POC in large tropical rivers. From the measured biospheric POC content and variability in annual sediment yield, we calculate a biospheric POC flux of 2.2(+1.3)(-0.9) teragrams of carbon per year from the Mackenzie River, which is three times the CO2 drawdown by silicate weathering in this basin. Offshore, we find evidence for efficient terrestrial organic carbon burial over the Holocene period, suggesting that erosion of organic carbon-rich, high-latitude soils may result in an important geological CO2 sink. PMID:26245581

  10. Environmental Drivers of Global Riverine Organic Carbon Age

    NASA Astrophysics Data System (ADS)

    McIntosh, H.; Buffam, I. D.; McCallister, S. L.

    2015-12-01

    The transport of terrestrial organic carbon (OC) to downstream systems via the fluvial network represents a "leakage" of terrestrial net primary production. The age of OC exported ranges from modern OC, derived from surficial soils and leaf litter, to ancient OC that had been stored for millennia on land. The age and ultimately the fate of this OC has ramifications for both the terrestrial carbon balance and the anthropogenic CO2 budget. Consequently, it is critical to understand the environmental and landscape associated factors that influence the age of OC laterally transferred to aquatic systems. We compiled radiocarbon data for both dissolved OC (DOC) (n = 670) and particulate OC (POC) (n = 722) for both rivers and streams. Sampling locations (n = 382) and their associated watersheds (1x10-2 km2 to 4.7x106 km2) encompassed a range from 38.7 oS to 74.9 oN. These radiocarbon values were paired with associated ancillary data, when available (OC concentration, δ13C), and subsequently combined with a spatial dataset developed in ArcGIS for corresponding watersheds. The spatial dataset contained a range of landscape parameters including mean elevation, relief, mean slope, and stream order as well as soil typology and land use. Δ14CDOC ranged from -974 ‰ to +383 ‰ (mean = 3 ‰, standard deviation (s.d.) = 150 ‰) and Δ14CPOC ranged from -992 ‰ to +227 ‰ (mean = -234 ‰, s.d. = 253 ‰) demonstrating a trend of younger DOC relative to its particulate counterpart. Landscape characteristics were first analyzed for their influence on radiocarbon ages of DOC and POC at a global scale. The data were then aggregated by biome (n = 14) to assess the role of regional environmental characteristics (i.e. precipitation, temperature, soil organic carbon) on DOC and POC age. Models were derived to determine the principle drivers of the radiocarbon age of OC in streams and rivers, among the landscape and environmental characteristics, for each biome.

  11. Organic Carbon Sources in Coastal Southeast Alaskan Streams

    NASA Astrophysics Data System (ADS)

    Hood, E.; Edwards, R. T.; D'Amore, D. V.; Lange, B. J.

    2003-12-01

    Dissolved organic matter (DOM) is abundant in southeast Alaskan watersheds and plays an important role in the biological and physical processes in these aquatic systems. Nearly 30% of the land area in southeast Alaska is classified as wetlands, a large proportion of which are peatlands. Peatlands are thought to provide substantial DOM to surface waters. Another important source of carbon to streams is spawning anadromous salmon. This study examines how streamwater concentrations of DOC are influenced by 1) catchments soils and vegetation, particularly wetland extent and 2) the presence or absence of anadromous fish. Our goal is to characterize the quantity and quality of different DOM sources and to develop an understanding of how these sources influence seasonal trends in streamwater DOM in coastal freshwater systems in southeast Alaska. Surface water and well samples were collected on two contrasting streams near Juneau, Alaska: Peterson Creek, a brownwater, high-carbon stream in a wetland-dominated catchment and McGinnis Creek, a clearwater stream draining upland spruce forest and alpine tundra. Both streams have runs of pink, coho, and chum salmon from July-September. Streamwater DOC concentrations on Peterson Creek averaged 5-6 mg C L-1 during the early summer and increased to 8-12 mg C L-1 during late July and August. Streamwater DOC concentrations on McGinnis Creek were typically less than 1 mg C L-1 during the early summer but increased dramatically to 4-9 mg C L-1 during spates in August. Well samples collected upslope from the streamwater sampling sites on Peterson and McGinnis Creeks had a similar range in DOC concentrations (10-40 mg C L-1), however the wells on McGinnis Creek showed much higher seasonal variability. Our initial results suggest that the seasonal increase in DOC in both streams is primarily associated with the flushing of soluble organic carbon from catchment soils by late summer rains. However, leaching of DOC from salmon carcasses may

  12. Use of inorganic dryer-salts in the determination of organic contaminants in air

    SciTech Connect

    Simonov, V.A.

    1985-09-01

    This paper presents results of a study of the adsorptive activity of a number of inorganic salts relative to water vapor and to organic vapors in air under the dynamic conditions which are uses in the indicator tube method. Data are also given on the properties of dryer salts having a surface modified with glycerin. It is shown that lithium chloride on porcelain and potassium carbonate having a surface modified with glycerin can be used to dry air in determining contaminants of nonpolar and polar organic substances in it. Anhydrone on porcelain, calcium chloride, and potassium carbonate absorb some substances which are being determined and therefore are less suitable.

  13. Soil organic carbon of an intensively reclaimed region in China: Current status and carbon sequestration potential.

    PubMed

    Deng, Xunfei; Zhan, Yu; Wang, Fei; Ma, Wanzhu; Ren, Zhouqiao; Chen, Xiaojia; Qin, Fangjin; Long, Wenli; Zhu, Zhenling; Lv, Xiaonan

    2016-09-15

    Land reclamation has been highly intensive in China, resulting in a large amount of soil organic carbon (SOC) loss to the atmosphere. Evaluating the factors which drive SOC dynamics and carbon sequestration potential in reclaimed land is critical for improving soil fertility and mitigating global warming. This study aims to determine the current status and factors important to the SOC density in a typical reclaimed land located in Eastern China, where land reclamation has been undergoing for centuries. A total of 4746 topsoil samples were collected from 2007 to 2010. The SOC density of the reclaimed land (3.18±0.05kgCm(-2); mean±standard error) is significantly lower than that of the adjacent non-reclaimed land (5.71±0.04kgCm(-2)) (p<0.05). A Random Forest model is developed and it captures the relationships between the SOC density and the environmental/anthropogenic factors (R(2)=0.59). The soil pH, land use, and elevation are the most important factors for determining SOC dynamics. In contrast, the effect of the reclamation age on the SOC density is negligible, where SOC content in the land reclaimed during years 1047-1724 is as low as that reclaimed during years 1945-2004. The scenario analysis results indicate that the carbon sequestration potential of the reclaimed lands may achieve a maximum of 5.80±1.81kgCO2m(-2) (mean±SD) when dryland is converted to flooded land with vegetable-rice cropping system and soil pH of ~5.9. Note that in some scenarios the methane emission substantially offsets the carbon sequestration potential, especially for continuous rice cropping system. With the optimal setting for carbon sequestration, it is estimated that the dryland reclaimed in the last 50years in China is able to sequester 0.12milliontons CO2 equivalent per year. PMID:27196991

  14. [Soil organic carbon fractionation methods and their applications in farmland ecosystem research: a review].

    PubMed

    Zhang, Guo; Cao, Zhi-ping; Hu, Chan-juan

    2011-07-01

    Soil organic carbon is of heterogeneity in components. The active components are sensitive to agricultural management, while the inert components play an important role in carbon fixation. Soil organic carbon fractionation mainly includes physical, chemical, and biological fractionations. Physical fractionation is to separate the organic carbon into active and inert components based on the density, particle size, and its spatial distribution; chemical fractionation is to separate the organic carbon into various components based on the solubility, hydrolizability, and chemical reactivity of organic carbon in a variety of extracting agents. In chemical fractionation, the dissolved organic carbon is bio-available, including organic acids, phenols, and carbohydrates, and the acid-hydrolyzed organic carbon can be divided into active and inert organic carbons. Simulated enzymatic oxidation by using KMnO4 can separate organic carbon into active and non-active carbon. Biological fractionation can differentiate microbial biomass carbon and potential mineralizable carbon. Under different farmland management practices, the chemical composition and pool capacity of soil organic carbon fractions will have different variations, giving different effects on soil quality. To identify the qualitative or quantitative relationships between soil organic carbon components and carbon deposition, we should strengthen the standardization study of various fractionation methods, explore the integrated application of different fractionation methods, and sum up the most appropriate organic carbon fractionation method or the appropriate combined fractionation methods for different farmland management practices. PMID:22007474

  15. Experimental determination of carbon dioxide evolution during aerobic composting of agro-wastes.

    PubMed

    Tripathi, Shilpa; Srivastava, J K

    2012-10-01

    This work aims at optimal composting of agro-wastes like sugarcane bagasse, wood straw and soya husk. A mixture of these substances along with small quantity of food waste as the seed was composted aerobically and carbon dioxide evolved was determined experimentally using a composting system comprising aerobic digester, operating in near-optimal conditions with regard to adequacy of oxygen and temperature in the system. During aerobic composting of agro-waste carbon dioxide is produced due to degradation of different carbon fractions in the substrate. Carbon dioxide production rate, which is a measure of bacterial/fungal activity in composting systems, can be related to various process parameters like different carbon fractions present in the substrate and their reaction rates, progress and termination of compost phenomenon and stabilization of organic matter. This gives a balanced compromise between complexity of mathematical model and extensive experimentation, and can be used for determining optimum conditions for composting. PMID:25151714

  16. Light absorption by organic carbon from wood combustion

    NASA Astrophysics Data System (ADS)

    Chen, Y.; Bond, T. C.

    2009-09-01

    Carbonaceous aerosols affect the radiative balance of the Earth by absorbing and scattering light. While BC is highly absorbing, some organic compounds also have significant absorption, which is greater at near-ultraviolet and blue wavelengths. To the extent that OC absorbs visible light, it may be a non-negligible contributor to direct aerosol radiative forcing. In this work, we examine absorption by primary OC emitted from solid fuel pyrolysis. We provide absorption spectra of this material, which can be related to the imaginary refractive index. This material has polar character but is not fully water-soluble: more than 92% was extractable by methanol or acetone, compared with 73% for water and 52% for hexane. Water-soluble organic carbon contributed to light absorption at both ultraviolet and visible wavelengths. However, a larger portion came from organic carbon that is extractable only by methanol. The spectra of water-soluble organic carbon are similar to others in the literature. We compared spectra for material generated with different wood type, wood size and pyrolysis temperature. Higher wood temperature is the main factor creating organic aerosol with higher absorption, causing about a factor of four increase in mass-normalized absorption at visible wavelengths. A simple model suggests that, despite the absorption, both high-temperature and low-temperature carbon have negative climate forcing over a surface with average albedo.

  17. Stock assessment and balance of organic carbon in the Eastern European steppe ecosystems tree windbreaks

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Reserves and balance of organic carbon in ecosystems of windbreaks planted in the mid-1950s within the Forest-Steppe of Central Eastern Europe were determined from field sampling. Windbreaks were represented by 5-6-row plantings of Populus nigra and Betula pendula ("Streletskaya Steppe"), Acer negun...

  18. TOWARDS A STANDARD METHOD FOR THE MEASUREMENT OF ORGANIC CARBON IN SEDIMENTS

    EPA Science Inventory

    The precisions achieved by two different methods for analysis of organic carbon in soils and sediments were determined and compared. The first method is a rapid dichromate oxidation technique (Walkley-Black) that has long been a standard in soil chemistry. The second is an automa...

  19. The influence of organic carbon flux on benthic foraminiferal proxies

    NASA Astrophysics Data System (ADS)

    Corliss, B. H.; Sun, X.; Brown, C. W.; Showers, W. J.

    2005-12-01

    During the last 30 years, deep-sea benthic foraminifera have been widely used in reconstructing environmental conditions in the deep sea. Initial suggestions of faunal-water mass associations were never substantiated and, instead, organic carbon flux was identified as a primary influence on species and assemblage patterns. Organic carbon flux also impacts the chemistry of deep water masses and is reflected in the stable isotopic and trace element composition of a number of deep-sea taxa. The timing of delivery of organic carbon can also have an affect on foraminiferal chemistry. Carbon-13 data of Holocene Epistominella exigua from the North Atlantic show a 0.9 per mil change over 60 degrees of latitude that can be correlated to seasonality of productivity, based on a comparison of SeaWIFS satellite imagery. Seasonality and mean annual primary productivity do not affect the carbon-13 of Planulina wuellerstorfi in the North Atlantic, although P. wuellerstorfi exhibits significant variability. Our results suggest that the carbon-13 of E. exigua in conjunction with P. wuellerstorfi can be used to reconstruct seasonality of primary productivity. These findings raise the possibility that other geochemical proxies influenced by particle flux from the surface may be affected by periodic flux events that create phytodetritus layers and change the chemistry of the microhabitats occupied by some benthic foraminiferal species. Existing studies suggest that organic carbon flux and seasonality of flux influence both faunal and geochemical signals from benthic foraminiferal. These relationships can be used to reconstruct primary productivity and seasonality, in addition to deep-water circulation, and illustrate the importance of incorporating ecological information in the interpretation of geochemical data from deep sea taxa.

  20. Semicontinuous automated measurement of organic carbon in atmospheric aerosol samples.

    PubMed

    Lu, Chao; Rashinkar, Shilpa M; Dasgupta, Purnendu K

    2010-02-15

    A fully automated measurement system for ambient aerosol organic carbon, capable of unattended operation over extended periods, is described. Particles are collected in a cyclone with water as the collection medium. The collected sample is periodically aspirated by a syringe pump into a holding loop and then delivered to a wet oxidation reactor (WOR). Acid is added, and the WOR is purged to measure dissolved CO(2) or inorganic carbonates (IC) as evolved CO(2). The IC background can often be small and sufficiently constant to be corrected for, without separate measurement, by a blank subtraction. The organic material is now oxidized stepwise or in one step to CO(2). The one-step oxidation involves UV-persulfate treatment in the presence of ozone. This treatment converts organic carbon (OC) to CO(2), but elemental carbon is not oxidized. The CO(2) is continuously purged from solution and collected by two sequential miniature diffusion scrubbers (DSs), a short DS preceding a longer one. Each DS consists of a LiOH-filled porous hydrophobic membrane tube with terminal stainless steel tubes that function as conductance-sensing electrodes. As CO(2) is collected by the LiOH-filled DSs, hydroxide is converted into carbonate and the resulting decrease in conductivity is monitored. The simultaneous use of the dual short and long DS units bearing different concentrations of LiOH permits both good sensitivity and a large dynamic range. The limit of detection (LOD, S/N = 3) is approximately 140 ng of C. With a typical sampling period of 30 min at a sampling rate of 30 L/min, this corresponds to an LOD of 160 ng/m(3). The approach also provides information on the ease of oxidation of the carbonaceous aerosol and hence the nature of the carbon contained therein. Ambient aerosol organic carbon data are presented. PMID:20092351

  1. Catalytic Coupling of Carbon Dioxide with Terpene Scaffolds: Access to Challenging Bio-Based Organic Carbonates.

    PubMed

    Fiorani, Giulia; Stuck, Moritz; Martín, Carmen; Belmonte, Marta Martínez; Martin, Eddy; Escudero-Adán, Eduardo C; Kleij, Arjan W

    2016-06-01

    The challenging coupling of highly substituted terpene oxides and carbon dioxide into bio-based cyclic organic carbonates catalyzed by Al(aminotriphenolate) complexes is reported. Both acyclic as well as cyclic terpene oxides were used as coupling partners, showing distinct reactivity/selectivity behavior. Whereas cyclic terpene oxides showed excellent chemoselectivity towards the organic carbonate product, acyclic substrates exhibited poorer selectivities owing to concomitant epoxide rearrangement reactions and the formation of undesired oligo/polyether side products. Considering the challenging nature of these coupling reactions, the isolated yields of the targeted bio-carbonates are reasonable and in most cases in the range 50-60 %. The first crystal structures of tri-substituted terpene based cyclic carbonates are reported and their stereoconnectivity suggests that their formation proceeds through a double inversion pathway. PMID:27159151

  2. Selective Sorption of Dissolved Organic Carbon Compounds by Temperate Soils

    SciTech Connect

    Jagadamma, Sindhu; Mayes, Melanie; Phillips, Jana Randolph

    2012-01-01

    Physico-chemical sorption of dissolved organic carbon (DOC) on soil minerals is one of the major processes of organic carbon (OC) stabilization in soils, especially in deeper layers. The attachment of C on soil solids is related to the reactivity of the soil minerals and the chemistry of the sorbate functional groups, but the sorption studies conducted without controlling microbial activity may overestimate the sorption potential of soil. This study was conducted to examine the sorptive characteristics of a diverse functional groups of simple OC compounds (D-glucose, L-alanine, oxalic acid, salicylic acid, and sinapyl alcohol) on temperate climate soil orders (Mollisols, Ultisols and Alfisols) with and without biological degradative processes. Equilibrium batch experiments were conducted using 0-100 mg C L-1 at a solid-solution ratio of 1:60 for 48 hrs and the sorption parameters were calculated by Langmuir model fitting. The amount of added compounds that remained in the solution phase was detected by high performance liquid chromatography (HPLC) and total organic C (TOC) analysis. Soil sterilization was performed by -irradiation technique and experiments were repeated to determine the contribution of microbial degradation to apparent sorption. Overall, Ultisols did not show a marked preference for apparent sorption of any of the model compounds, as indicated by a narrower range of maximum sorption capacity (Smax) of 173-527 mg kg soil-1 across compounds. Mollisols exhibited a strong preference for apparent sorption of oxalic acid (Smax of 5290 mg kg soil-1) and sinapyl alcohol (Smax of 2031 mg kg soil-1) over the other compounds. The propensity for sorption of oxalic acid is mainly attributed to the precipitation of insoluble Ca-oxalate due to the calcareous nature of most Mollisol subsoils and its preference for sinapyl alcohol could be linked to the polymerization of this lignin monomer on 2:2 mineral dominated soils. The reactivity of Alfisols to DOC was in

  3. Spatial distribution of soil organic carbon stocks in France

    NASA Astrophysics Data System (ADS)

    Martin, M. P.; Wattenbach, M.; Smith, P.; Meersmans, J.; Jolivet, C.; Boulonne, L.; Arrouays, D.

    2010-11-01

    Soil organic carbon plays a major role in the global carbon budget, and can act as a source or a sink of atmospheric carbon, whereby it can influence the course of climate change. Changes in soil organic soil stocks (SOCS) are now taken into account in international negotiations regarding climate change. Consequently, developing sampling schemes and models for estimating the spatial distribution of SOCS is a priority. The French soil monitoring network has been established on a 16 km × 16 km grid and the first sampling campaign has recently been completed, providing circa 2200 measurements of stocks of soil organic carbon, obtained through an in situ composite sampling, uniformly distributed over the French territory. We calibrated a boosted regression tree model on the observed stocks, modelling SOCS as a function of other variables such as climatic parameters, vegetation net primary productivity, soil properties and land use. The calibrated model was evaluated through cross-validation and eventually used for estimating SOCS for the whole of metropolitan France. Two other models were calibrated on forest and agricultural soils separately, in order to assess more precisely the influence of pedo-climatic variables on soil organic carbon for such soils. The boosted regression tree model showed good predictive ability, and enabled quantification of relationships between SOCS and pedo-climatic variables (plus their interactions) over the French territory. These relationship strongly depended on the land use, and more specifically differed between forest soils and cultivated soil. The total estimate of SOCS in France was 3.260 ± 0.872 PgC for the first 30 cm. It was compared to another estimate, based on the previously published European soil organic carbon and bulk density maps, of 5.303 PgC. We demonstrate that the present estimate might better represent the actual SOCS distributions of France, and consequently that the previously published approach at the European

  4. Origin of particulate organic carbon in the marine atmosphere as indicated by it stable carbon isotopic composition

    SciTech Connect

    Chesselet, R.; Fontugne, M.; Buat-Menard, P.; Ezat, U.; Lambert, C.E.

    1981-04-01

    Organic carbon concentration and isotopic composition were determined in samples of atmospheric particulate matter collected in 1979 at remote marine locations (Enewetak atoll, Sargasso Sea) during the SEAREX (Sea-Air Exchange) program field experiments. Atmospheric Particulate Organic Carbon (POC) concentrations were found to be in the range of 0.3 to 1.2 mg. m/sup -3/, in agreement with previous literature data. The major mass of POC was found on the smallest particles (r<0.5 mm). The /sup 13/C//sup 12/C of the small particles is close to the one expected (d/sup 13/C = 26 +- 2/sup 0///sub infinity/) for atmospheric POC of continental origin. For all the samples analysed so far, it appears that more than 80% of atmospheric POC over remote marine areas is of continental origin. This can be explained either by long-range transport of small sized continental organic aserosols or by the production of POC in the marine atmosphere from a vapor phase organic carbon pool of continental origin. The POC in the large size fraction of marine aerosols (<20% of the total concentration) is likely to have a direct marine origin since its carbon isotopic composition is close to the expected value (d/sup 13/C = -21 +- 2/sup 0///sub 00/) for POC associated with sea-salt droplets transported to the marine atmosphere.

  5. [Determination of carbon dioxide released from soil at different humidities].

    PubMed

    Imshenetskiĭ, A A; Murzakov, B G

    1978-01-01

    The detection of soil microorganisms by their evolution of carbon dioxide does not always correlate with the number of microorganisms and the rate of biochemical processes in soil. New microbial populations appear in the incubation chamber as the concentration of carbon dioxide increases; this results in an increase in the activity of such processes as photosynthesis, chemosynthesis and heterotrophic assimilation of carbon dioxide. Life detection on other planets by determining carbon dioxide evolved from the ground may lead to erroneous conclusions on the presence of microorganism in the ground. PMID:745559

  6. Ultrasonic Spraying of Carbon Nanotubes using Organic Solvents

    NASA Astrophysics Data System (ADS)

    Willey, Anthony; Davis, Robert; Vanfleet, Richard

    2012-10-01

    Because of their unique electrical and mechanical properties, thin films of carbon nanotubes have several potential applications, especially in the fields of organic electronics and photovoltaics. We present a method for spraying thin films of nanotubes that have been suspended in organic solvents N-methyl Pyrollidone (NMP) and N-Cyclohexyl-2-pyrrolidone (CHP). The sprayed nanotubes are randomly oriented, and films are transparent, conductive, and mechanically stable.

  7. Standardizing Organic Carbon Measurements for Modern and Geologic Timescales

    NASA Astrophysics Data System (ADS)

    Wang, R. Z.; Yager, J. A.; Rollins, N.; Berelson, W.; West, A. J.; Li, G.

    2015-12-01

    Accurate reconstruction of carbon isotope records (as well as accurate characterization of the modern carbon cycle, e.g., in soils) relies on reliably separating organic carbon (Corg) from carbonate-derived carbon (Ccarb). These fractions are characterized by very different isotope composition, so small carbonate contamination can strongly bias Corg results, and vice versa. Several criteria must be met for accurate %C and d13C analysis. In the case of analyzing Corg, these include: (1) Ccarb must be removed through a process called "decarbonation." (2) Ccarb can be removed by acid dissolution, but if the acid is too strong then the Corg itself may solubilize, causing inaccurate results. (3) The preparation process for decarbonation can also unintentionally add carbon to samples and create a methodological blank that also will bias results. This study tested decarbonation methods with the above criteria in mind. The focus was on (i) heated treatment with weak liquid acid, e.g., 1M HCl ("liquid phase decarbonation") and (ii) heated treatment with vapor from concentrated acid ("vapor phase decarbonation"). Our results confirm that heated treatment is critical to producing reliable records; recalcitrant carbonate phases are not removed during room temperature decarbonation and can bias carbon isotope values. Vapor phase decarbonation may prevent loss in solution that is known to occur using liquid phase methods. However, our results show that blanks must be very carefully monitored and can be a concern during vapor phase treatment. Moreover, we still observe some loss of organics during vapor phase treatment, as evidenced by changes in Corg and d13C with length of reaction time. The length of vapor phase treatment must be carefully considered depending on the type of sample being tested. Overall, our work emphasizes the importance of carefully considering sample-specific decarbonation methodology in order to produce reliable values for %Corg and d13C.

  8. Are we overestimating organic carbon concentrations in soils containing inorganic carbon?

    NASA Astrophysics Data System (ADS)

    Cunliffe, Andrew; Brazier, Richard; Vernon, Ian

    2014-05-01

    The concentration of carbon in soils is often measured via chromatographic analysis of elemental gases following dry combustion of a soil sample. This quantifies total carbon (TC), and, in soils which can be assumed to contain no inorganic carbon (IC), TC can be interpreted as organic carbon (OC). Soils containing IC are commonly subjected to an acid digestion to remove IC, prior to analysis for OC concentration; with IC being assigned as the difference between TC and OC. However, the removal of IC reduces the sample mass. Therefore, analysing acid-washed samples reveals the carbon concentration of the non-inorganic carbon sample mass, rather than the actual sample mass, as is generally assumed. This results in the overestimation of OC concentrations and consequent underestimation of IC concentrations, although TC concentrations are correct. The magnitude of the error is proportional to both IC concentration, and the ratio OC/IC, and consequently is greater in carbonate-rich samples. We present a revised protocol for accurately calculating OC and IC concentrations, using the carbon concentrations of the total sample and the acid-washed sample. The revised protocol is easily applicable to existing data, and corrects a known bias in apportioning carbon between organic and inorganic pools. Propagating the error through an example dataset from a semiarid environment, we find it can make a substantial (>10%) difference to estimated total OC pools. We recommend that this new protocol is used whenever elemental analysers are used to quantify OC concentrations in acid-washed sediments.

  9. Isotopic Composition of Organic and Inorganic Carbon in Desert Biological Soil Crust Systems

    NASA Astrophysics Data System (ADS)

    Alexander, K.; Hartnett, H.; Anbar, A.; Beraldi, H.; Garcia-Pichel, F.

    2006-12-01

    Biological soil crusts (BSCs) are microbial communities that colonize soil surfaces in many arid regions. BSCs are important sources for fixed carbon and nitrogen in these ecosystems, and they greatly influence the structure, function, and appearance of desert soils. Biological activity of BSCs occurs during pulses of hydration requiring desert crusts to tolerate extremes in UV radiation, temperature, and desiccation. These characteristics make desert crusts unique systems that have received little consideration in the study of biogeochemical processes in extreme environments. This project investigates the impact of BSCs on carbon dynamics within desert soils. Soil cores ranging in depth from 8 to 12 cm were taken in March, 2006 from deserts near Moab, Utah. Two major BSC classes were identified: lichen-dominated (dark and pinnacled) soil crusts and cyanobacteria-dominated (light and flat) soil crusts. These two surface morphologies are related to the different biological communities. Carbon content and stable carbon isotopic composition were determined for the bulk carbon pool, as well as for the organic and inorganic carbon fractions of the soils. Expectedly, there was a net decrease in organic carbon content with depth (0.39-0.27 percent). Stable carbon isotope values for the organic fraction ranged from -5.8 per mil to -24.0 per mil (Avg: -14.4 per mil, S.D: 6.42 per mil). Stable carbon isotope values for the inorganic fraction ranged from 0.3 per mil to -3.6 per mil (Avg: -2.4 per mil, S.D.: 1.05 per mil). The variation in the isotopic composition of the organic carbon was due to a strong depletion below the surface soil value occurring between 3 and 5 cm depth, with an enrichment above the original surface value at depths below 6 to 10 cm. These data suggest that within desert soil crust systems the carbon isotopic signal is complex with both a clear biological imprint (lighter organic carbon) as well as evidence for some mechanism that results in

  10. [Effects of straw application and earthworm inoculation on soil labile organic carbon].

    PubMed

    Yu, Jian-Guang; Li, Hui Xin; Chen, Xiao-Yun; Hu, Feng

    2007-04-01

    A six-year field plot experiment of rice-wheat rotation was conducted to study the effects of straw application and earthworm inoculation on cropland soil organic carbon and labile organic carbon. Five treatments were installed, i.e., CK, straw mulch (M), straw mulch plus earthworm inoculation (ME), incorporated straw with soil (I), and incorporated straw with soil plus earthworm inoculation (IE). The results showed that soil organic carbon content increased significantly after six years straw application, and treatment I was more efficient than treatment M. Earthworm inoculation under straw application had no significant effects on soil organic carbon content. Straw application, whether straw mulch or incorporated straw with soil, increased the content of soil labile organic carbon, and incorporated straw with soil was more beneficial to the increase of the contents of hot water-extractable carbon, potentially mineralizable carbon, acid-extractable carbon, readily oxidizable carbon, particulate organic carbon, and light fraction organic carbon. There was a little relationship between the quantitative variations of soil dissoluble organic carbon and microbial biomass carbon and the patterns of straw application. Among the treatments, the activity of soil organic carbon was decreased in the order of IF > I > M > ME > CK. Straw application pattern was the main factor affecting soil organic carbon and labile organic carbon, while earthworm inoculation was not universally significanfly effective to all kinds of soil labile organic carbon. PMID:17615878

  11. Bacterial survival governed by organic carbon release from senescent oceanic phytoplankton

    NASA Astrophysics Data System (ADS)

    Lasternas, S.; Agustí, S.

    2013-10-01

    Bacteria recycle vast amounts of organic carbon, playing key biogeochemical and ecological roles in the ocean. Bacterioplankton dynamics are expected to be dependent on phytoplankton primary production, but there is a high diversity of processes (e.g. sloppy feeding, cell exudation, viral lysis) involved in the transference of primary production to dissolved organic carbon available to bacteria. Here we show cell survival of heterotrophic bacterioplankton in the subtropical Atlantic Ocean to be determined by phytoplankton extracellular carbon release (PER). PER represents the fraction of primary production released as dissolved organic carbon, and changes in the PER variability was explained by phytoplankton cell death, with the communities experiencing the highest phytoplankton cell mortality showing a larger proportion of extracellular carbon release. Both PER and the percent of dead phytoplankton cells increased from eutrophic to oligotrophic waters, while heterotrophic bacteria communities, including 60 to 95% of living cells (%LC), increased from the productive to the most oligotrophic waters. The percentage of living heterotrophic bacterial cells increased with increasing phytoplankton extracellular carbon release, across oligotrophic to productive waters in the NE Atlantic, where lower PER have resulted in a decrease in the flux of phytoplankton DOC per bacterial cell. The results highlight phytoplankton cell death as a process influencing the flow of dissolved photosynthetic carbon in the NE Atlantic Ocean, and demonstrated a close coupling between the fraction of primary production released and heterotrophic bacteria survival.

  12. Estimations of Soil organic carbons pools in Southern Greenland

    NASA Astrophysics Data System (ADS)

    Ogric, Mateja; Chellasamy, Menaka; Knadel, Maria; Greve, Mogens H.; Adhikari, Kabindra; Jakobsen, Bjarne H.; Kristiansen, Søren M.

    2015-04-01

    Terrestrial areas hold large pools of soil organic carbon (SOC), which is a fundamental soil feature. It is known that SOC can be destabilized due to climate changes and land use, what can lead to accelerated emissions of greenhouse gasses into the atmosphere. Arctic soil, which is strongly sensitive to climate changes, stores about 14% of the Earth's organic carbon (Elberling et al., 2004). Therefore, the high-latitude soils are an important factor for investigation and determination of carbon pools. Recent advances in analytical methods offer various improvements regarding data acquisition. For example, near-infrared spectroscopy (NIRS) analyses of soils is often cost-effective and faster as compared to traditional wet-chemical methods for C and N determination, while it also gives reliable results. The aim of this study is i) to estimate the SOC pool in a remote area with poor soil data, i.e. Southern Greenland, and ii) to compare estimation techniques based on two independent SOC analytical approaches. The study area comprises approx. 17,500 km2 large non-glaciated land in south Greenland, from the Labrador Sea coast line to the margins of the Greenland Ice Sheet (46° 47'W-44° 16'W and 60° 07'N-61° 24'N). A large number of the abandoned Norse Viking Age settlements, i.e. Gardar, Hvalsø and Igaliku, are found here. A soil resource database was compiled from existing sources and recently collected soil samples to improve the data density for the area. The majority of the dataset represents 233 soil samples, which were collected in summer 2013 following Globalsoilmap.net specifications (Ogric et al., 2014). The focus of the investigation was on the top soil (down to 25 cm depth). These samples were analyzed for total soil carbon, nitrogen, and sulphur contents. The NIRS method was used on the same soil samples in an attempt to improve the data interpretation. Chemometric methods of NIRS data were applied with The Unscrambler X (Camo, 2014). Next, all known

  13. Quantification of functional soil organic carbon pools in a chronosequence of land abandonment in southern Spain.

    NASA Astrophysics Data System (ADS)

    Trigalet, Sylvain; Gabarrón-Galeote, Miguel A.; Van Oost, Kristof; van Wesemael, Bas

    2015-04-01

    Land abandonment is the dominant land use change in the Mediterranean, and determines the soil organic carbon (SOC) as the vegetation recovers during secondary succession. The rate of SOC recovery is influenced by environmental factors such as precipitation, soil properties or other local factors. Using aerial photographs taken in 1956, 1977, 1984, 1998, 2001 and 2009, a chronosequence of crop land abandonment was designed and topsoil samples were taken at each stage of recovery in a region North of Málaga. As SOC is a mixture of functional pools, it is important to isolate organic carbon with distinct functional properties to better understand the overall dynamic over decades. Using fractionation scheme introduced by Zimmermann et al. (2007), five fractions were isolated based on particle size, density and resistance: particulate organic matter (POM), dissolved organic carbon (DOC), SOC linked to silt and clay (s & c), SOC attached to sand particles or occluded in aggregates (S+A) and a chemically resistant fraction obtained by NaOCl oxidation (rSOC). Although there were no significant changes in particle-size distribution between the recovery stages (except for the croplands), there was a significant increase of S+A fraction over time (16 to 38%) at the expense of the s & c fraction (84 to 58%), indicating aggregation processes. Carbon concentrations within fractions S+A or rSOC did not change over time. Rather, carbon associated with silt and clay particles (s &c) was significantly affected after a few decades of abandonment. It increased from 5.7 gC.kg-1 in croplands to 10.3 gC.kg-1 in semi-natural plots. The chronosequence showed that carbon can be stored in more stable fractions. Taking into account active carbon (DOC + POM) and intermediate carbon (s & c, S+A) as indicators for carbon dynamics, we showed that the proportion of active carbon increased from 11% to 34% within the chronosequence. On the other hand, the proportion of slow cycling carbon

  14. Organic matter diagenesis in shallow water carbonate sediments

    NASA Astrophysics Data System (ADS)

    Ingalls, Anitra E.; Aller, Robert C.; Lee, Cindy; Wakeham, Stuart G.

    2004-11-01

    Muddy carbonate deposits near the Dry Tortugas, Florida, are characterized by high organic carbon remineralization rates. However, approximately half of the total sedimentary organic matter potentially supporting remineralization is occluded in CaCO 3 minerals (intracrystalline). While a portion of nonintracrystalline organic matter appears to cycle rapidly, intracrystalline organic matter has an approximately constant concentration with depth, suggesting that as long as its protective mineral matrix is intact, it is not readily remineralized. Organic matter in excess of intracrystalline organic matter that is preserved may have a variety of mineral associations (e.g., intercrystalline, adsorbed or detrital). In surface sediment, aspartic acid contributed ˜22 mole % and ˜50 mole % to nonintracrystalline and intracrystalline pools, respectively. In deeper sediment (1.6-1.7m), the composition of hydrolyzable amino acids in both pools was similar (aspartic acid ˜40 mole %). Like amino acids, intracrystalline and nonintracrystalline fatty acids have different compositions in surface sediments, but are indistinguishable at depth. These data suggest that preserved organic matter in the nonintracrystalline pool is stabilized by its interactions with CaCO 3. Neutral lipids are present in very low abundances in the intracrystalline pool and are extensively degraded in both the intracrystalline and nonintracrystalline pools, suggesting that mineral interactions do not protect these compounds from degradation. The presence of chlorophyll- a, but absence of phytol, in the intracrystalline lipid pool demonstrates that chloropigments are present only in the nonintracrystalline pool. Sedimentary chloropigments decrease with depth at similar rates in Dry Tortugas sediments as found in alumino-silicate sediments from the Long Island Sound, suggesting that chloropigment degradation is largely unaffected by mineral interactions. Overall, however, inclusion and protection of

  15. Organic carbon production, mineralization and preservation on the Peruvian margin

    NASA Astrophysics Data System (ADS)

    Dale, A. W.; Sommer, S.; Lomnitz, U.; Montes, I.; Treude, T.; Gier, J.; Hensen, C.; Dengler, M.; Stolpovsky, K.; Bryant, L. D.; Wallmann, K.

    2014-09-01

    Carbon cycling in Peruvian margin sediments (11° S and 12° S) was examined at 16 stations from 74 m on the inner shelf down to 1024 m water depth by means of in situ flux measurements, sedimentary geochemistry and modeling. Bottom water oxygen was below detection limit down to ca. 400 m and increased to 53 μM at the deepest station. Sediment accumulation rates and benthic dissolved inorganic carbon fluxes decreased rapidly with water depth. Particulate organic carbon (POC) content was lowest on the inner shelf and at the deep oxygenated stations (< 5%) and highest between 200 and 400 m in the oxygen minimum zone (OMZ, 15-20%). The organic carbon burial efficiency (CBE) was unexpectedly low on the inner shelf (< 20%) when compared to a global database, for reasons which may be linked to the frequent ventilation of the shelf by oceanographic anomalies. CBE at the deeper oxygenated sites was much higher than expected (max. 81%). Elsewhere, CBEs were mostly above the range expected for sediments underlying normal oxic bottom waters, with an average of 51 and 58% for the 11° S and 12° S transects, respectively. Organic carbon rain rates calculated from the benthic fluxes alluded to a very efficient mineralization of organic matter in the water column, with a Martin curve exponent typical of normal oxic waters (0.88 ± 0.09). Yet, mean POC burial rates were 2-5 times higher than the global average for continental margins. The observations at the Peruvian margin suggest that a lack of oxygen does not affect the degradation of organic matter in the water column but promotes the preservation of organic matter in marine sediments.

  16. Organic carbon flux and particulate organic matter composition in Arctic valley glaciers: examples from the Bayelva River and adjacent Kongsfjorden

    NASA Astrophysics Data System (ADS)

    Zhu, Zhuo-Yi; Wu, Ying; Liu, Su-Mei; Wenger, Fred; Hu, Jun; Zhang, Jing; Zhang, Rui-Feng

    2016-02-01

    In the face of ongoing global warming and glacier retreat, the composition and flux of organic matter in glacier-fjord systems are key variables for updating the carbon cycle and budget, whereas the role of Arctic valley glaciers seems unimportant when compared with the huge Greenland Ice Sheet. Our field observations of the glacier-fed Bayelva River, Svalbard, and the adjacent Kongsfjorden allowed us to determine the compositions of particulate organic matter from glacier to fjord and also to estimate the flux of organic carbon, both for the river and for Svalbard in general. Particulate organic carbon (POC) and dissolved organic carbon (DOC) in the Bayelva River averaged 56 and 73 µM, respectively, in August, 2012. Amino acids (AAs) and phytoplankton carbon accounted for ˜ 10 % of the bulk POC in the Bayelva River, while AAs represented > 90 % of particulate nitrogen (PN) in fjord surface water, suggesting the strong in situ assimilation of organic matter. Bacteria accounted for 13 and 19 % of the POC in the Bayelva River and the Kongsfjorden, respectively, while values for PN were much higher (i.e., 36 % in Kongsfjorden). The total discharge from the Bayelva River in 2012 was 29 × 106 m3. Furthermore, we calculated the annual POC, DOC, and PN fluxes for the river as 20 ± 1.6 tons, 25 ± 5.6 tons, and 4.7 ± 0.75 tons, respectively. Using the POC content and DOC concentration data, we then estimated the annual POC and DOC fluxes for Svalbard glaciers. Although the estimated POC (0.056 ± 0.02 × 106 tons year-1) and DOC (0.02 ± 0.01 × 106 tons year-1) fluxes of Svalbard glaciers are small in amount, its discharge-weighted flux of DOC was over twice higher than other pan-Arctic glacier systems, suggesting its important role as a terrestrial DOC source.

  17. Organic carbon cycling in landfills: Model for a continuum approach

    SciTech Connect

    Bogner, J.; Lagerkvist, A.

    1997-09-01

    Organic carbon cycling in landfills can be addressed through a continuum model where the end-points are conventional anaerobic digestion of organic waste (short-term analogue) and geologic burial of organic material (long-term analogue). Major variables influencing status include moisture state, temperature, organic carbon loading, nutrient status, and isolation from the surrounding environment. Bioreactor landfills which are engineered for rapid decomposition approach (but cannot fully attain) the anaerobic digester end-point and incur higher unit costs because of their high degree of environmental isolation and control. At the other extreme, uncontrolled land disposal of organic waste materials is similar to geologic burial where organic carbon may be aerobically recycled to atmospheric CO{sub 2}, anaerobically converted to CH{sub 4} and CO{sub 2} during early diagenesis, or maintained as intermediate or recalcitrant forms into geologic time (> 1,000 years) for transformations via kerogen pathways. A family of improved landfill models are needed at several scales (molecular to landscape) which realistically address landfill processes and can be validated with field data.

  18. Carbonaceous aerosols influencing atmospheric radiation: Black and organic carbon

    SciTech Connect

    Penner, J.E.

    1994-09-01

    Carbonaceous particles in the atmosphere may both scatter and absorb solar radiation. The fraction associated with the absorbing component is generally referred to as black carbon (BC) and is mainly produced from incomplete combustion processes. The fraction associated with condensed organic compounds is generally referred to as organic carbon (OC) or organic matter and is mainly scattering. Absorption of solar radiation by carbonaceous aerosols may heat the atmosphere, thereby altering the vertical temperature profile, while scattering of solar radiation may lead to a net cooling of the atmosphere/ocean system. Carbonaceous aerosols may also enhance the concentrations of cloud condensation nuclei. This paper summarizes observed concentrations of aerosols in remote continental and marine locations and provides estimates for the fine particle (D < 2.5 {mu}m) source rates of both OC and BC. The source rates for anthropogenic organic aerosols may be as large as the source rates for anthropogenic sulfate aerosols, suggesting a similar magnitude of direct forcing of climate. The role of BC in decreasing the amount of reflected solar radiation by OC and sulfates is discussed. The total estimated forcing depends on the source estimates for organic and black carbon aerosols which are highly uncertain. The role of organic aerosols acting as cloud condensation nuclei (CCN) is also described.

  19. 42 CFR 422.566 - Organization determinations.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... for temporarily out of the area renal dialysis services, emergency services, post-stabilization care... treatment. (5) Failure of the MA organization to approve, furnish, arrange for, or provide payment...

  20. Analysis of isotope and organic carbon signatures in hillslope hydrographs

    NASA Astrophysics Data System (ADS)

    Dusek, Jaromir; Vogel, Tomas; Dohnal, Michal; Jankovec, Jakub; Sanda, Martin; Votrubova, Jana

    2015-04-01

    Headwater catchments are among the most important areas for investigation of isotope and carbon fluxes because their small sizes best enable separation of above- and below ground compartments for improved understanding of the respective transport mechanisms. So far, only few studies utilized stable isotope information in modeling and even fewer linked dissolved carbon fluxes to mixing or transport models. Stable isotopes of water and dissolved organic carbon provide basis for studying transport processes ranging from soil profile scale to hillslope and catchment scale. In this study, stormflow dynamics of oxygen-18 and dissolved organic carbon was analyzed using a physically based modeling approach. One-dimensional dual-continuum vertical flow and transport model, based on Richards and advection-dispersion equations, was used to simulate the subsurface processes during significant rainfall-runoff episodes of a summer season. Water flow and transport of solutes were assumed to take place in two mutually communicating continua, the soil matrix and the network of preferential pathways. Oxygen-18 and dissolved organic carbon were observed in soil water, stormflow discharge in the experimental hillslope trench, and stream discharge at the catchment outlet. In the present study, we analyzed the transformation of input solute signals into signatures observed in the stormflow discharge. The research was supported by the Czech Science Foundation Project No. 14-15201J.

  1. An isotopic study of biogeochemical relationships between carbonates and organic carbon in the Greenhorn Formation

    NASA Technical Reports Server (NTRS)

    Hayes, J. M.; Popp, Brian N.; Takigiku, Ray; Johnson, Marcus W.

    1989-01-01

    Carbon-isotopic compositions of total carbonate, inoceramid carbonate, micritic carbonate, secondary cements, total organic carbon, and geoporphyrins have been measured in 76 different beds within a 17-m interval of a core through the Greenhorn Formation, an interbedded limestone and calcareous shale unit of Cretaceous age from the Western Interior Seaway of North America. Results are considered in terms of variations in the processes of primary production and in secondary processes. It is shown that the porphyrin isotopic record reflects primary isotopic variations more closely than the TOC isotopic record and that, in these sediments, TOC is enriched in C-13 relative to its primary precursor by 0.6 to 2.8 percent. This enrichment is attributed to isotope effects within the consumer foodweb and is associated with respiratory heterotrophy. Variation in this secondary enrichment are correlated with variations in the isotopic composition of marine carbonate.

  2. Assessment of bacterial growth and total organic carbon removal on granular activated carbon contactors.

    PubMed Central

    Bancroft, K; Maloney, S W; McElhaney, J; Suffet, I H; Pipes, W O

    1983-01-01

    The overall growth rate of bacteria on granular activated carbon (GAC) contactors at the Philadelphia Torresdale Water Treatment Pilot Plant facility was found to decrease until steady state was reached. The growth rate was found to fluctuate between 6.94 X 10(-3) and 8.68 X 10(-4) doublings per h. The microbiological removal of total organic carbon (TOC) was calculated by considering the GAC contactors as semiclosed continuous culture systems and using growth yield factors determined in laboratory experiments. After ozonation, the average TOC entering the contactors was 1,488 micrograms/liter, and the average effluent TOC was 497 micrograms/liter. Microbiological TOC removal was found to average 240 micrograms/liter on GAC contactors, which was not significantly different from microbiological TOC (220 micrograms/liter) removal across a parallel sand contactor where no adsorption took place. Thus, GAC did not appear to enhance biological TOC removal. Bacterial growth and maintenance was responsible for approximately 24% of the TOC removal on GAC under the conditions of this study. PMID:6639023

  3. Aerosol organic carbon to black carbon ratios: Analysis ofpublished data and implications for climate forcing

    SciTech Connect

    Novakov, T.; Menon, S.; Kirchstetter, T.W.; Koch, D.; Hansen, J.E.

    2005-07-11

    Measurements of organic carbon (OC) and black carbon (BC)concentrations over a variety of locations worldwide, have been analyzed to infer the spatial distributions of the ratios of OC to BC. Since these ratios determine the relative amounts of scattering and absorption, they are often used to estimate the radiative forcing due to aerosols. An artifact in the protocol for filter measurements of OC has led to widespread overestimates of the ratio of OC to BC in atmospheric aerosols. We developed a criterion to correct for this artifact and analyze corrected OC to BC ratios. The OC to BC ratios, ranging from 1.3to 2.4, appear relatively constant and are generally unaffected by seasonality, sources or technology changes, at the locations considered here. The ratios compare well with emission inventories over Europe and China but are a factor of two lower in other regions. The reduced estimate for OC/BC in aerosols strengthens the argument that reduction of soot emissions maybe a useful approach to slow global warming.

  4. Assessing Impacts of 20 yr Old Miscanthus on Soil Organic Carbon Quality

    NASA Astrophysics Data System (ADS)

    Hu, Yaxian; Schäfer, Gerhard; Kuhn, Nikolaus

    2015-04-01

    The use of biomass as a renewable energy source has become increasingly popular in Upper Rhine Region to meet the demand for renewable energy. Miscanthus is one of the most favorite biofuel crops, due to its long life and large yields, as well as low energy and fertilizer inputs. However, current research on Miscanthus is mostly focused on the techniques and economics to produce biofuel or the impacts of side products such as ash and sulfur emissions to human health. Research on the potential impacts of Miscanthus onto soil quality, especially carbon quality after long-term adoption, is very limited. Some positive benefits, such as sequestrating organic carbon, have been repeatedly reported in previous research. Yet the quality of newly sequestrated organic carbon and its potential impacts onto global carbon cycling remain unclear. To fully account for the risks and benefits of Miscanthus, it is required to investigate the quality as well as the potential CO2 emissions of soil organic carbon on Miscanthus fields. As a part of the Interreg Project to assess the environmental impacts of biomass production in the Upper Rhine Region, this study aims to evaluate the carbon quality and the potential CO2 emissions after long-term Miscanthus adoption. Soils were sampled at 0-10, 10-40, 40-70, and 70-100 cm depths on three Miscanthus fields with up to 20 years of cultivation in Ammerzwiller France, Münchenstein Switzerland, and Farnsburg Switzerland. Soil texture, pH, organic carbon and nitrogen content were measured for each sampled layer. Topsoils of 0-10 cm and subsoils of 10-40 cm were also incubated for 40 days to determine the mineralization potential of the soil organic matter. Our results show that: 1) only in top soils of 0-10 cm, the 20 year old Miscanthus field has significantly higher soil organic carbon concentrations, than the control site. No significant differences were observed in deeper soil layers. Similar tendencies were also observed for organic

  5. Determination of nicotine, tar, volatile organic compounds and carbonyls in mainstream cigarette smoke using a glass filter and a sorbent cartridge followed by the two-phase/one-pot elution method with carbon disulfide and methanol.

    PubMed

    Uchiyama, Shigehisa; Hayashida, Hideki; Izu, Rina; Inaba, Yohei; Nakagome, Hideki; Kunugita, Naoki

    2015-12-24

    We have developed a new analytical method for the determination of nicotine, tar, volatile organic compounds and carbonyls in main-stream cigarette smoke using a sorbent cartridge packed with Carboxen 572 (CX-572) and a Cambridge filter pad (CFP) followed by the two-phase/one-pot elution method. A CX-572 cartridge is installed between the intake of the CFP and the pump of the smoking machine. Gaseous compounds collected with the CX-572 cartridge and total particulate matter (TPM) collected with the CFP are coeluted simultaneously in the same vial and then analyzed by high-performance liquid chromatography (HPLC), gas chromatography-mass spectrometry (GC/MS) and gas chromatograph-thermal conductivity detector (GC/TCD). Carbonyl compounds are determined by adding derivatizing reagent (2,4-dinitrophenylhydrazine, DNPH) to the eluate followed by HPLC analysis. VOCs and nicotine are determined by GC/MS, and water is determined by GC/TCD. The same sample eluate solution is used for HPLC, GC/MS and GC/TCD analyses. As a result of measuring main-stream cigarette smoke generated from reference cigarettes, almost all carbonyl compounds and VOCs except formaldehyde were passed through a CFP and trapped in a CX-572 cartridge. 100% of nicotine, tar and TPM were trapped in a CFP. 50% of water and 53% of formaldehyde were trapped in a CFP. The one-pot data is almost equal to the sums of CFP (particulate matter) and CX-572 (gaseous compounds) data. The two-phase/one-pot elution method can simultaneously measure nicotine, tar, volatile organic compounds and carbonyl compounds in cigarette smoke with simple operation and small amounts of reagents. PMID:26653840

  6. Organic Matter Quality and its Influence on Carbon Turnover and Stabilization in Northern Peatlands

    NASA Astrophysics Data System (ADS)

    Turetsky, M. R.; Wieder, R. K.

    2002-12-01

    Peatlands cover 3-5 % of the world's ice-free land area, but store about 33 % of global terrestrial soil carbon. Peat accumulation in northern regions generally is controlled by slow decomposition, which may be limited by cold temperatures and water-logging. Poor organic matter quality also may limit decay, and microbial activity in peatlands likely is regulated by the availability of labile carbon and/or nutrients. Conversely, carbon in recalcitrant soil structures may be chemically protected from microbial decay, particularly in peatlands where carbon can be buried in anaerobic soils. Soil organic matter quality is controlled by plant litter chemical composition and the susceptibility of organic compounds to decomposition through time. There are a number of techniques available for characterizing organic quality, ranging from chemical proximate or elemental analysis to more qualitative methods such as nuclear magenetic resonance, pyrolysis/mass spectroscopy, and Fourier transform infrared spectroscopy. We generally have relied on proximate analysis for quantitative determination of several organic fractions (i.e., water-soluble carbohydrates, soluble nonpolars, water-soluble phenolics, holocellulose, and acid insoluble material). Our approaches to studying organic matter quality in relation to C turnover in peatlands include 1) 14C labelling of peatland vegetation along a latitudinal gradient in North America, allowing us to follow the fate of 14C tracer in belowground organic fractions under varying climates, 2) litter bag studies focusing on the role of individual moss species in litter quality and organic matter decomposition, and 3) laboratory incubations of peat to explore relationships between organic matter quality and decay. These studies suggest that proximate organic fractions vary in lability, but that turnover of organic matter is influenced both by plant species and climate. Across boreal peatlands, measures of soil recalcitrance such as acid

  7. Elevated rates of organic carbon, nitrogen, and phosphorus accumulation in a highly impacted mangrove wetland

    NASA Astrophysics Data System (ADS)

    Sanders, Christian J.; Eyre, Bradley D.; Santos, Isaac R.; Machado, Wilson; Luiz-Silva, Wanilson; Smoak, Joseph M.; Breithaupt, Joshua L.; Ketterer, Michael E.; Sanders, Luciana; Marotta, Humberto; Silva-Filho, Emmanoel

    2014-04-01

    The effect of nutrient enrichment on mangrove sediment accretion and carbon accumulation rates is poorly understood. Here we quantify sediment accretion through radionuclide tracers to determine organic carbon (OC), total nitrogen (TN), and total phosphorus (TP) accumulation rates during the previous 60 years in both a nutrient-enriched and a pristine mangrove forest within the same geomorphological region of southeastern Brazil. The forest receiving high nutrient loads has accumulated OC, TN, and TP at rates that are fourfold, twofold, and eightfold respectively, higher than those from the undisturbed mangrove. Organic carbon and TN stable isotopes (δ13C and δ15N) reflect an increased presence of organic matter (OM) originating with either phytoplankton, benthic algae, or another allochthonous source within the more rapidly accumulated sediments of the impacted mangrove. This suggests that the accumulation rate of OM in eutrophic mangrove systems may be enhanced through the addition of autochthonous and allochthonous nonmangrove material.

  8. Soil Organic Carbon Dynamics under Conservation Agricultural Systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soil organic carbon (SOC) is a key element in the valuation of natural resources and the evaluation of how management affects soil quality and ecosystem services derived from soil. This paper describes a summary of some recent research aimed at understanding how SOC contributes to (a) various soil ...

  9. Impacts of soil organic carbon on soil physical behavior

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Management-induced changes in soil organic carbon (SOC) concentration can affect soil physical behavior. Specifically, removal of crop residues as biofuel may thus adversely affect soil attributes by reducing SOC concentration as crop residues are the main source of SOC. Implications of crop residue...

  10. Redistribution of soil and soil organic carbon on agricultural landscapes

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Patterns of soil organic carbon (SOC) vary widely across the landscape leading to large uncertainties in the SOC budgets for agricultural systems especially for landscapes where water, tillage, and wind erosion redistributes soil and SOC across the landscape. It is often assumed that soil erosion r...

  11. Photoproduction of Carbon Monoxide from Natural Organic Matter

    EPA Science Inventory

    Pioneering studies by Valentine provided early kinetic results that used carbon monoxide (CO) production to evaluate the photodecomposition of aquatic natural organic matter (NOM) . (ES&T 1993 27 409-412). Comparatively few kinetic studies have been conducted of the photodegradat...

  12. Isotope tracers of organic carbon during artificial recharge

    SciTech Connect

    Davisson, M.L.

    1998-02-09

    This project developed an analytical technique for measuring the isotope abundance for 14C and 13C in total organic carbon (TOC) in order to test whether these measurements can trace TOC interaction with sedimentary material at the bottom of rivers and lakes, soils, and subsurface aquifer rocks.

  13. REMOTE MONITORING OF ORGANIC CARBON IN SURFACE WATERS

    EPA Science Inventory

    This study shows that the intensity of the Raman normalized fluorescence emission induced in surface waters by ultraviolet radiation can be used to provide a unique remote sensing capability for airborne monitoring the concentration of dissolved organic carbon (DOC). Trace concen...

  14. Importance of unburned coal carbon, black carbon, and amorphous organic carbon to phenanthrene sorption in sediments.

    PubMed

    Cornelissen, Gerard; Gustafsson, Orjan

    2005-02-01

    The aim of this paper was to estimate the contribution to total phenanthrene sorption from unburned coal and black carbon (BC; soot and charcoal) in sediment. We determined sorption isotherms for five Argonne Premium Coal standards over a wide concentration interval (0.01-10 000 ng/L). The coals showed strong and nonlinear sorption (carbon-normalized K(F) = 5.41-5.96; nF = 0.68-0.82). Coal sorption appeared to become more nonlinear with increasing coal maturity. The coal's specific surface area appeared to influence K(F). On the basis of the current coal sorption observations combined with earlier petrographic analyses and BC sorption experiments, we calculated for one particular sediment that coal, BC, and "other" OC were all important to PHE sorption in the environmentally relevant nanogram per liter range. This indicates that it is important to consider strong sorption to coal in the risk assessment of coal-impacted geosorbents (e.g., river beds) where coal is mined/shipped and manufactured gas plant sites. PMID:15757337

  15. Spatial distribution of soil organic carbon stocks in France

    NASA Astrophysics Data System (ADS)

    Martin, M. P.; Wattenbach, M.; Smith, P.; Meersmans, J.; Jolivet, C.; Boulonne, L.; Arrouays, D.

    2011-05-01

    Soil organic carbon plays a major role in the global carbon budget, and can act as a source or a sink of atmospheric carbon, thereby possibly influencing the course of climate change. Changes in soil organic carbon (SOC) stocks are now taken into account in international negotiations regarding climate change. Consequently, developing sampling schemes and models for estimating the spatial distribution of SOC stocks is a priority. The French soil monitoring network has been established on a 16 km × 16 km grid and the first sampling campaign has recently been completed, providing around 2200 measurements of stocks of soil organic carbon, obtained through an in situ composite sampling, uniformly distributed over the French territory. We calibrated a boosted regression tree model on the observed stocks, modelling SOC stocks as a function of other variables such as climatic parameters, vegetation net primary productivity, soil properties and land use. The calibrated model was evaluated through cross-validation and eventually used for estimating SOC stocks for mainland France. Two other models were calibrated on forest and agricultural soils separately, in order to assess more precisely the influence of pedo-climatic variables on SOC for such soils. The boosted regression tree model showed good predictive ability, and enabled quantification of relationships between SOC stocks and pedo-climatic variables (plus their interactions) over the French territory. These relationships strongly depended on the land use, and more specifically, differed between forest soils and cultivated soil. The total estimate of SOC stocks in France was 3.260 ± 0.872 PgC for the first 30 cm. It was compared to another estimate, based on the previously published European soil organic carbon and bulk density maps, of 5.303 PgC. We demonstrate that the present estimate might better represent the actual SOC stock distributions of France, and consequently that the previously published approach at the

  16. Inorganic carbon and fossil organic carbon are source of bias for quantification of sequestered carbon in mine spoil

    NASA Astrophysics Data System (ADS)

    Vindušková, Olga; Frouz, Jan

    2016-04-01

    Carbon sequestration in mine soils has been studied as a possibility to mitigate the rising atmospheric CO2 levels and to improve mine soil quality (Vindu\\vsková and Frouz, 2013). Moreover, these soils offer an unique opportunity to study soil carbon dynamics using the chronosequence approach (using a set of sites of different age on similar parent material). However, quantification of sequestered carbon in mine soils is often complicated by fossil organic carbon (e.g., from coal or kerogen) or inorganic carbon present in the spoil. We present a methodology for quantification of both of these common constituents of mine soils. Our recommendations are based on experiments done on post-mining soils in Sokolov basin, Czech Republic. Here, fossil organic carbon is present mainly as kerogen Type I and II and represents 2-6 wt.% C in these soils. Inorganic carbon in these soils is present mainly as siderite (FeCO3), calcite (CaCO3), and dolomite (CaMg(CO3)2). All of these carbonates are often found in the overburden of coal seams thus being a common constituent of post-mining soils in the world. Vindu\\vsková O, Frouz J, 2013. Soil carbon accumulation after open-cast coal and oil shale mining in Northern Hemisphere: a quantitative review. ENVIRONMENTAL EARTH SCIENCES, 69: 1685-1698. Vindu\\vsková O, Dvořáček V, Prohasková A, Frouz J. 2014. Distinguishing recent and fossil organic matter - A critical step in evaluation of post-mining soil development - using near infrared spectroscopy. ECOLOGICAL ENGINEERING. 73: 643-648. Vindu\\vsková O, Sebag D, Cailleau G, Brus J, Frouz J. 2015. Methodological comparison for quantitative analysis of fossil and recently derived carbon in mine soils with high content of aliphatic kerogen. ORGANIC GEOCHEMISTRY, 89-90:14-22.

  17. Dynamics of the Particulate Organic Carbon in the southern Baltic Sea.

    NASA Astrophysics Data System (ADS)

    Dzierzbicka-Glowacka, L.; Maciejewska, A.; Kuliński, K.; Pempkowiak, J.

    2009-04-01

    This paper presents a one-dimensional Particulate Organic Carbon Dynamic Model 1D-POCD. The particulate organic carbon concentration is determined as the sum of phytoplankton, zooplankton and dead organic matter (detritus) concentrations. Mathematically, the pelagic variables of 1D-POCD model are described by a second-order partial differential equation of the diffusion type with biogeochemical sources and sinks. The temporal changes in the phytoplankton biomass are caused by primary production, respiration, mortality, grazing by zooplankton and sinking. The zooplankton biomass is affected by ingestion, excretion, respiration, fecal production, mortality, and carnivorous grazing. The changes in the pelagic detritus concentration are determined by input of: dead phytoplankton and zooplankton, natural mortality of predators, fecal pellets, and sinks: sedimentation, zooplankton grazing and decomposition. The 1D-POCD model was used to simulate the seasonal dynamics of particulate organic carbon fluxes in the southern Baltic Sea (Gdańsk Deep, Bornholm Deep and Gotland Deep). The results of the simulations were compared with the mean concentrations of particulate organic carbon recorded in situ at station situated at the Gdańsk Deep. Generally good agreement between the measured and modeled POC concentration was obtained.

  18. Hyperspectral Analysis of Soil Nitrogen, Carbon, Carbonate, and Organic Matter Using Regression Trees

    PubMed Central

    Gmur, Stephan; Vogt, Daniel; Zabowski, Darlene; Moskal, L. Monika

    2012-01-01

    The characterization of soil attributes using hyperspectral sensors has revealed patterns in soil spectra that are known to respond to mineral composition, organic matter, soil moisture and particle size distribution. Soil samples from different soil horizons of replicated soil series from sites located within Washington and Oregon were analyzed with the FieldSpec Spectroradiometer to measure their spectral signatures across the electromagnetic range of 400 to 1,000 nm. Similarity rankings of individual soil samples reveal differences between replicate series as well as samples within the same replicate series. Using classification and regression tree statistical methods, regression trees were fitted to each spectral response using concentrations of nitrogen, carbon, carbonate and organic matter as the response variables. Statistics resulting from fitted trees were: nitrogen R2 0.91 (p < 0.01) at 403, 470, 687, and 846 nm spectral band widths, carbonate R2 0.95 (p < 0.01) at 531 and 898 nm band widths, total carbon R2 0.93 (p < 0.01) at 400, 409, 441 and 907 nm band widths, and organic matter R2 0.98 (p < 0.01) at 300, 400, 441, 832 and 907 nm band widths. Use of the 400 to 1,000 nm electromagnetic range utilizing regression trees provided a powerful, rapid and inexpensive method for assessing nitrogen, carbon, carbonate and organic matter for upper soil horizons in a nondestructive method. PMID:23112620

  19. Hyperspectral analysis of soil nitrogen, carbon, carbonate, and organic matter using regression trees.

    PubMed

    Gmur, Stephan; Vogt, Daniel; Zabowski, Darlene; Moskal, L Monika

    2012-01-01

    The characterization of soil attributes using hyperspectral sensors has revealed patterns in soil spectra that are known to respond to mineral composition, organic matter, soil moisture and particle size distribution. Soil samples from different soil horizons of replicated soil series from sites located within Washington and Oregon were analyzed with the FieldSpec Spectroradiometer to measure their spectral signatures across the electromagnetic range of 400 to 1,000 nm. Similarity rankings of individual soil samples reveal differences between replicate series as well as samples within the same replicate series. Using classification and regression tree statistical methods, regression trees were fitted to each spectral response using concentrations of nitrogen, carbon, carbonate and organic matter as the response variables. Statistics resulting from fitted trees were: nitrogen R(2) 0.91 (p < 0.01) at 403, 470, 687, and 846 nm spectral band widths, carbonate R(2) 0.95 (p < 0.01) at 531 and 898 nm band widths, total carbon R(2) 0.93 (p < 0.01) at 400, 409, 441 and 907 nm band widths, and organic matter R(2) 0.98 (p < 0.01) at 300, 400, 441, 832 and 907 nm band widths. Use of the 400 to 1,000 nm electromagnetic range utilizing regression trees provided a powerful, rapid and inexpensive method for assessing nitrogen, carbon, carbonate and organic matter for upper soil horizons in a nondestructive method. PMID:23112620

  20. Efficient organic carbon burial in the Bengal fan sustained by the Himalayan erosional system.

    PubMed

    Galy, Valier; France-Lanord, Christian; Beyssac, Olivier; Faure, Pierre; Kudrass, Hermann; Palhol, Fabien

    2007-11-15

    Continental erosion controls atmospheric carbon dioxide levels on geological timescales through silicate weathering, riverine transport and subsequent burial of organic carbon in oceanic sediments. The efficiency of organic carbon deposition in sedimentary basins is however limited by the organic carbon load capacity of the sediments and organic carbon oxidation in continental margins. At the global scale, previous studies have suggested that about 70 per cent of riverine organic carbon is returned to the atmosphere, such as in the Amazon basin. Here we present a comprehensive organic carbon budget for the Himalayan erosional system, including source rocks, river sediments and marine sediments buried in the Bengal fan. We show that organic carbon export is controlled by sediment properties, and that oxidative loss is negligible during transport and deposition to the ocean. Our results indicate that 70 to 85 per cent of the organic carbon is recent organic matter captured during transport, which serves as a net sink for atmospheric carbon dioxide. The amount of organic carbon deposited in the Bengal basin represents about 10 to 20 per cent of the total terrestrial organic carbon buried in oceanic sediments. High erosion rates in the Himalayas generate high sedimentation rates and low oxygen availability in the Bay of Bengal that sustain the observed extreme organic carbon burial efficiency. Active orogenic systems generate enhanced physical erosion and the resulting organic carbon burial buffers atmospheric carbon dioxide levels, thereby exerting a negative feedback on climate over geological timescales. PMID:18004382

  1. Tracing organic compounds in aerobically altered methane-derived carbonate pipes (Gulf of Cadiz, SW Iberia)

    NASA Astrophysics Data System (ADS)

    Merinero, Raúl; Ruiz-Bermejo, Marta; Menor-Salván, César; Lunar, Rosario; Martínez-Frías, Jesús

    2012-07-01

    The primary geochemical process at methane seeps is anaerobic oxidation of methane (AOM), performed by methanotrophic archaea and sulfate-reducing bacteria (SRB). The molecular fingerprints (biomarkers) of these chemosynthetic microorganisms can be preserved in carbonates formed through AOM. However, thermal maturity and aerobic degradation can change the original preserved compounds, making it difficult to establish the relation between AOM and carbonate precipitation. Here we report a study of amino acid and lipid abundances in carbonate matrices of aerobically altered pipes recovered from the seafloor of the Gulf of Cadiz (SW Iberian Peninsula). This area is characterized by a complex tectonic regime that supports numerous cold seeps. Studies so far have not determined whether the precipitation of carbonate pipes in the Gulf of Cadiz is a purely chemical process or whether microbial communities are involved. Samples from this site show signs of exposure to oxygenated waters and of aerobic alteration, such as oxidation of authigenic iron sulfides. In addition, the degradation index, calculated from the relative abundance of preserved amino acids, indicates aerobic degradation of organic matter. Although crocetane was the only lipid identified from methanotrophic archaea, the organic compounds detected (n-alkanes, regular isoprenoids and alcohols) are compatible with an origin from AOM coupled with bacterial sulfate reduction (BSR) and subsequent aerobic degradation. We establish a relation among AOM, BSR and pipe formation in the Gulf of Cadiz through three types of analysis: (1) stable carbon and oxygen isotopic composition of carbonate minerals; (2) carbonate microfabrics; and (3) mineralogical composition. Our results suggest that carbonate pipes may form through a process similar to the precipitation of vast amounts of carbonate pavements often found at cold seeps. Our approach suggests that some organic compound patterns, in combination with additional

  2. Determination and evaluation of organic balances of alumina refineries

    SciTech Connect

    Solymar, K.; Gimpel-Kazar, M.; Molnar, E.

    1996-10-01

    The adequate measures to control the organic level and especially that of humates and oxalate need the determination and evaluation of the organic balance of the given alumina plant. The organic materials of the different alumina refineries have special compositions, therefore it is very difficult and limited to draw general and common conclusions for all alumina refineries concerning the role and control of organics. The methodology of the determination of the organic balance of an alumina plant will be discussed. The qualitative and quantitative determination of organic materials has been performed by means of gas-chromatography of the esterized organic materials. The organic balances of three different alumina refineries will be compared and evaluated relating to the total organic and oxalate contents.

  3. Organic Carbon Storage in Four Ecosystem Types in the Karst Region of Southwestern China

    PubMed Central

    Wang, Shijie; Guo, Ke; Yang, Jun; Zhang, Xinshi; Li, Guoqing

    2013-01-01

    Karst ecosystems are important landscape types that cover about 12% of the world's land area. The role of karst ecosystems in the global carbon cycle remains unclear, due to the lack of an appropriate method for determining the thickness of the solum, a representative sampling of the soil and data of organic carbon stocks at the ecosystem level. The karst region in southwestern China is the largest in the world. In this study, we estimated biomass, soil quantity and ecosystem organic carbon stocks in four vegetation types typical of karst ecosystems in this region, shrub grasslands (SG), thorn shrubbery (TS), forest - shrub transition (FS) and secondary forest (F). The results showed that the biomass of SG, TS, FS, and F is 0.52, 0.85, 5.9 and 19.2 kg m−2, respectively and the corresponding organic cabon storage is 0.26, 0.40, 2.83 and 9.09 kg m−2, respectively. Nevertheless, soil quantity and corresponding organic carbon storage are very small in karst habitats. The quantity of fine earth overlaying the physical weathering zone of the carbonate rock of SG, TS, FS and F is 38.10, 99.24, 29.57 and 61.89 kg m−2, respectively, while the corresponding organic carbon storage is only 3.34, 4.10, 2.37, 5.25 kg m−2, respectively. As a whole, ecosystem organic carbon storage of SG, TS, FS, and F is 3.81, 4.72, 5.68 and 15.1 kg m−2, respectively. These are very low levels compared to other ecosystems in non-karst areas. With the restoration of degraded vegetation, karst ecosystems in southwestern China may play active roles in mitigating the increasing CO2 concentration in the atmosphere. PMID:23451047

  4. Carbon and nitrogen abundances determined from transition layer lines

    NASA Technical Reports Server (NTRS)

    Boehm-Vitense, Erika; Mena-Werth, Jose

    1992-01-01

    The possibility of determining relative carbon, nitrogen, and silicon abundances from the emission-line fluxes in the lower transition layers between stellar chromospheres and coronae is explored. Observations for main-sequence and luminosity class IV stars with presumably solar element abundances show that for the lower transition layers Em = BT sup -gamma. For a given carbon abundance the constants gamma and B in this relation can be determined from the C II and C IV emission-line fluxes. From the N V and S IV lines, the abundances of these elements relative to carbon can be determined from their surface emission-line fluxes. Ratios of N/C abundances determined in this way for some giants and supergiants agree within the limits of errors with those determined from molecular bands. For giants, an increase in the ratio of N/C at B-V of about 0.8 is found, as expected theoretically.

  5. Improved soil carbonate determination by FT-IR and X-ray analysis

    NASA Astrophysics Data System (ADS)

    Bruckman, Viktor; Wriessnig, Karin

    2013-04-01

    In forest soils on calcareous parent material, carbonate is a key component which influences both chemical and physical soil properties and thus fertility and productivity. At low organic carbon contents it is difficult to distinguish between organic and inorganic carbon (carbonate) in soils. The common gas-volumetric method to determine carbonate has a number of disadvantages. We hypothesize that a combination of two spectroscopic methods, which account for different forms of carbonate, can be used to model soil carbonate in our study region. Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) was combined with X-ray diffraction (XRD) to develop a model based on partial least squares regression (PLSR). Results of the gas-volumetric Scheibler method were corrected for the calcite/dolomite ratio. The best model performance was achieved when we combined the two analytical methods using four principal components. The root mean squared error of prediction decreased from 13.07 to 11.57, while full cross-validation explained 94.5% of the variance of the carbonate content. This is the first time that a combination of the proposed methods has been used to predict carbonate in forest soils, offering a simple and cheap method to precisely estimate soil carbonate contents while increasing accuracy in comparison to spectroscopic approaches proposed earlier. This approach has the potential to complement or substitute gas-volumetric methods, specifically in study areas with low soil heterogeneity and similar parent material or in long-term monitoring by consecutive sampling. Reference: Bruckman, V. and K. Wriessnig, Improved soil carbonate determination by FT-IR and X-ray analysis. Environmental Chemistry Letters, 2012: p. 1-6. [DOI:DOI 10.1007/s10311-012-0380-4

  6. Organic carbon burial efficiency in a large tropical hydroelectric reservoir

    NASA Astrophysics Data System (ADS)

    Mendonça, R.; Kosten, S.; Sobek, S.; Cardoso, S. J.; Figueiredo-Barros, M. P.; Estrada, C. H. D.; Roland, F.

    2015-11-01

    Hydroelectric reservoirs bury significant amounts of organic carbon (OC) in their sediments. Many reservoirs are characterized by high sedimentation rates, low oxygen concentrations in bottom water, and a high share of terrestrially derived OC, and all of these factors have been linked to a high efficiency of OC burial. However, investigations of OC burial efficiency (OCBE, i.e. the ratio between OC buried and deposited) in reservoirs is limited to a few studies, none of which include spatially resolved analyses. In this study we determined the spatial variation in OCBE in a large tropical reservoir and related it to sediment characteristics. Our results show that the sediment accumulation rate explains up to 92 % of the spatial variability in OCBE, outweighing the effect of other variables, such as OC source and oxygen exposure time. OCBE at the pelagic sites varied from 48 to 86 % (mean 67 %) and decreased towards the dam. At the margins, OCBE was lower (9 to 17 %) due to the low sediment accumulation in shallow areas. Our data show that the variability in OCBE both along the rivers-dam and the margin-pelagic axes must be considered in whole-reservoir assessments. Combining these results with a spatially resolved assessment of sediment accumulation and OC burial in the studied reservoir, we estimated a whole-basin OC burial efficiency of 57 %. Being the first whole-basin assessment of OCBE in a reservoir, these results suggest that reservoirs may bury OC more efficiently than natural lakes.

  7. Organic carbon burial efficiency in a subtropical hydroelectric reservoir

    NASA Astrophysics Data System (ADS)

    Mendonça, Raquel; Kosten, Sarian; Sobek, Sebastian; Jaqueline Cardoso, Simone; Figueiredo-Barros, Marcos Paulo; Henrique Duque Estrada, Carlos; Roland, Fábio

    2016-06-01

    Hydroelectric reservoirs bury significant amounts of organic carbon (OC) in their sediments. Many reservoirs are characterized by high sedimentation rates, low oxygen concentrations in bottom water and a high share of terrestrially derived OC, and all of these factors have been linked to a high efficiency of OC burial. However, investigations of OC burial efficiency (OCBE, i.e., the ratio between buried and deposited OC) in reservoirs are limited to a few studies, none of which include spatially resolved analyses. In this study we determined the spatial variation in OCBE in a large subtropical reservoir and related it to sediment characteristics. Our results show that the sediment accumulation rate explains up to 92 % of the spatial variability in OCBE, outweighing the effect of other variables, such as OC source and oxygen exposure time. OCBE at the pelagic sites varied from 48 to 86 % (mean 67 %) and decreased towards the dam. At the margins, OCBE was lower (9-17 %) due to the low sediment accumulation in shallow areas. Our data show that the variability in OCBE both along the rivers-dam and the margin-pelagic axes must be considered in whole-reservoir assessments. Combining these results with a spatially resolved assessment of sediment accumulation and OC burial in the studied reservoir, we estimated a spatially resolved mean OC burial efficiency of 57 %. Being the first assessment of OCBE with such a high spatial resolution in a reservoir, these results suggest that reservoirs may bury OC more efficiently than natural lakes.

  8. Latitudinal Gradients in Degradation of Marine Dissolved Organic Carbon

    PubMed Central

    Arnosti, Carol; Steen, Andrew D.; Ziervogel, Kai; Ghobrial, Sherif; Jeffrey, Wade H.

    2011-01-01

    Heterotrophic microbial communities cycle nearly half of net primary productivity in the ocean, and play a particularly important role in transformations of dissolved organic carbon (DOC). The specific means by which these communities mediate the transformations of organic carbon are largely unknown, since the vast majority of marine bacteria have not been isolated in culture, and most measurements of DOC degradation rates have focused on uptake and metabolism of either bulk DOC or of simple model compounds (e.g. specific amino acids or sugars). Genomic investigations provide information about the potential capabilities of organisms and communities but not the extent to which such potential is expressed. We tested directly the capabilities of heterotrophic microbial communities in surface ocean waters at 32 stations spanning latitudes from 76°S to 79°N to hydrolyze a range of high molecular weight organic substrates and thereby initiate organic matter degradation. These data demonstrate the existence of a latitudinal gradient in the range of complex substrates available to heterotrophic microbial communities, paralleling the global gradient in bacterial species richness. As changing climate increasingly affects the marine environment, changes in the spectrum of substrates accessible by microbial communities may lead to shifts in the location and rate at which marine DOC is respired. Since the inventory of DOC in the ocean is comparable in magnitude to the atmospheric CO2 reservoir, such a change could profoundly affect the global carbon cycle. PMID:22216139

  9. Fossil organic carbon in Siberian Yedoma and thermokarst deposits

    NASA Astrophysics Data System (ADS)

    Strauss, J.; Schirrmeister, L.; Wetterich, S.

    2011-12-01

    During the late Quaternary, a large pool of organic carbon accumulated in the ice-rich syngenetic frozen deposits and soils preserved in the arctic and subarctic permafrost zone. Because of the potential release of organic carbon from degrading permafrost, the organic-matter (OM) inventory in Yedoma deposits and its degradation features are relevant to current concerns about the effects of global warming. In this context, it is essential to improve the understanding permafrost-stored OM composition and availability. The objective of this study is to develop an approach of OM quantification in frozen deposits including OM quality estimation. We analyzed OM characteristics like total organic carbon content, stable carbon isotopes and carbon-nitrogen ratios. Moreover, lipid biomarkers (alkanes, fatty acids and glycerol dialkyl glycerol tetraether) and sediment parameters like grain size and bulk density of Yedoma and thermokarst deposits exposed at Duvanny Yar (lower Kolyma River, Siberia) and the west coast of Buor Khaya Peninsula (Laptev Sea, Siberia) were studied. With the biomarker approach it is possible to distinguish deposits which were accumulated and frozen during the Pleistocene and Holocene. Biomarker indices, like the compound specific index, average chain length and tetraether characteristics supply feasible results for past permafrost environments. Late Pleistocene biomarker records indicate cold conditions during the growth/summer period for the late Pleistocene and generally low degradation of the stored OM. In contrast, Holocene thermokarst deposits indicate warmer conditions. The averaged volumetric OM content of the studied Yedoma and thermokarst deposits are greater than 10 kg/m^3 and do not exceed 30 kg/m^3. Given that Yedoma deposits accumulated at relatively fast rates and at low temperatures, the OM underwent a short time of decomposition before it was incorporated into a permanently-frozen state. Consequently, such deposits contain a labile

  10. Age of organic carbon of sediments flowing through an intermittent Mediterranean river basin

    NASA Astrophysics Data System (ADS)

    Boix-Fayos, Carolina; de Vente, Joris; Martínez-Mena, María; Almagro, María; Nadeu, Elisabet

    2015-04-01

    Fluvial sediments have the potential to bury large amounts of organic carbon (OC) annually, contributing to the terrestrial carbon sink. The temporal significance of this sink will strongly depend on the attributes of the sediment sources, that partially determine the characteristics of OC in sediments, and on the depositional environment, which influences the stability of sediments upon deposition. Knowledge of the age of the redistributed organic carbon could give us an indication of its origin and potential stability, however, little is known about the characteristics and age of organic carbon (OC) flowing through Mediterranean intermittent rivers. Several studies undertaken in an intermittent medium sized catchment (111 km2) in SE Spain showed how sediments flowing through the catchment, that were sampled during transport (suspended sediments) and at different depositional settings (sediment wedges, alluvial bars, delta, reservoir sediments), showed an OC content of approximately half of that in the soils of the drainage area (9.42±9.01 g kg-1 versus 20.45±7.71 g kg-1, respectively), with important variation between the explored sediment deposits. Selective sorting of mineral and organic material during transport and deposition increased from upstream towards downstream. A characterization of carbon ages from radiocarbon analysis showed much younger organic carbon in soils related directly to the vegetation cover (547±380 years BP with large variations between forest and agricultural soils) than in fluvial sediments. The sediments transported in suspension showed the oldest average age (7396±1640 years BP) coming probably from bedrock sources and petrogenic origin, compared to the sediments deposited in the delta-alluvial plain (3999±365 years BP) and compared to the relatively young carbon found in the reservoir-lake at the outlet of the catchment (1838±2000 BP with large variations depending on the sediment depth). Variation of organic carbon age with

  11. DETERMINATION OF ORGANIC EMISSIONS FROM NEW CARPETING

    EPA Science Inventory

    New carpeting has been the source of a number of indoor air health and odor complaints. nvestigations of a variety of carpet samples have shown that there is a diversity of organic emissions among carpet types; some of the compounds found have been listed in the NIOSH Registry of...

  12. Tracing the sources of organic carbon in freshwater systems

    NASA Astrophysics Data System (ADS)

    Glendell, Miriam; Meersmans, Jeroen; Barclay, Rachel; Yvon-Durocher, Gabriel; Barker, Sam; Jones, Richard; Hartley, Iain; Dungait, Jennifer; Quine, Timothy

    2016-04-01

    both terrestrial and aquatic sources as recorded in lake sediments to the measured rates of soil erosion and terrestrial & aquatic CO2 respiration rates, this study has paved a way towards a novel and cross-disciplinary approach to investigate and further improve current status of knowledge as regards C-cycling across the entire terrestrial-aquatic continuum. 137Cs was found to be useful to understand the dynamics and spatial pattern of lateral fluxes of sediment & C at the catchment scale, while tracing chemical composition of C using n-alkanes and stable isotopes (δ13C, δ15N) allowed distinguishing between the terrestrial vs. aquatic origin of C and determining main sources of particulate organic carbon in the aquatic environment within the two study catchments.

  13. Long-term tillage and drainage influences on soil organic carbon dynamics, aggregate stability, and corn yield

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Labile pools of soil organic carbon (SOC) and nitrogen (N) affect the carbon (C) and N fluxes from terrestrial soils, whereas, long-term C and N storage is determined by the long-lived recalcitrant fractions. Tillage influences these labile pools, however effect of the tillage systems may be differe...

  14. Qualitative determination of carbon black in food products.

    PubMed

    Miranda-Bermudez, E; Belai, N; Harp, B Petigara; Yakes, B J; Barrows, J N

    2012-01-01

    Carbon black (C.I. 77266) is an insoluble pigment produced by the partial combustion of hydrocarbons. The pigment is known by several synonyms, including vegetable carbon, lamp black and carbon ash, that correspond to the raw materials and methods used for its production. Vegetable carbon (E153) is permitted for use in colouring food in the European Union. The US Food and Drug Administration (USFDA) has not approved the use of any type of carbon black for colouring food, although the agency batch certifies the pigment as D&C Black No. 2 for use in colouring certain cosmetics. Since carbon black (as vegetable carbon) may be present in food products offered for import into the United States, the USFDA's district laboratories need a qualitative analytical method for determining its presence. We have developed an extraction method for this purpose. A sample is broken down and dissolved with nitric acid. The resulting solution is filtered and treated with hydrochloric acid to dissolve any black iron oxide also present as a colour additive. A black residue remaining on the filter paper indicates the presence of carbon black in the food. We confirmed the presence of carbon black in residues from several standards and food products using Raman spectroscopy. The limit of detection for this method is 0.0001%. PMID:22035229

  15. Adsorption of dissolved natural organic matter by modified activated carbons.

    PubMed

    Cheng, Wei; Dastgheib, Seyed A; Karanfil, Tanju

    2005-06-01

    Adsorption of dissolved natural organic matter (DOM) by virgin and modified granular activated carbons (GACs) was studied. DOM samples were obtained from two water treatment plants before (i.e., raw water) and after coagulation/flocculation/sedimentation processes (i.e., treated water). A granular activated carbon (GAC) was modified by high temperature helium or ammonia treatment, or iron impregnation followed by high temperature ammonia treatment. Two activated carbon fibers (ACFs) were also used, with no modification, to examine the effect of carbon porosity on DOM adsorption. Size exclusion chromatography (SEC) and specific ultraviolet absorbance (SUVA(254)) were employed to characterize the DOMs before and after adsorption. Iron-impregnated (HDFe) and ammonia-treated (HDN) activated carbons showed significantly higher DOM uptakes than the virgin GAC. The enhanced DOM uptake by HDFe was due to the presence of iron species on the carbon surface. The higher uptake of HDN was attributed to the enlarged carbon pores and basic surface created during ammonia treatment. The SEC and SUVA(254) results showed no specific selectivity in the removal of different DOM components as a result of carbon modification. The removal of DOM from both raw and treated waters was negligible by ACF10, having 96% of its surface area in pores smaller than 1 nm. Small molecular weight (MW) DOM components were preferentially removed by ACF20H, having 33% of its surface area in 1--3 nm pores. DOM components with MWs larger than 1600, 2000, and 2700 Da of Charleston raw, Charleston-treated, and Spartanburg-treated waters, respectively, were excluded from the pores of ACF20H. In contrast to carbon fibers, DOM components from entire MW range were removed from waters by virgin and modified GACs. PMID:15927230

  16. Aqueous adsorption and removal of organic contaminants by carbon nanotubes.

    PubMed

    Yu, Jin-Gang; Zhao, Xiu-Hui; Yang, Hua; Chen, Xiao-Hong; Yang, Qiaoqin; Yu, Lin-Yan; Jiang, Jian-Hui; Chen, Xiao-Qing

    2014-06-01

    Organic contaminants have become one of the most serious environmental problems, and the removal of organic contaminants (e.g., dyes, pesticides, and pharmaceuticals/drugs) and common industrial organic wastes (e.g., phenols and aromatic amines) from aqueous solutions is of special concern because they are recalcitrant and persistent in the environment. In recent years, carbon nanotubes (CNTs) have been gradually applied to the removal of organic contaminants from wastewater through adsorption processes. This paper reviews recent progress (145 studies published from 2010 to 2013) in the application of CNTs and their composites for the removal of toxic organic pollutants from contaminated water. The paper discusses removal efficiencies and adsorption mechanisms as well as thermodynamics and reaction kinetics. CNTs are predicted to have considerable prospects for wider application to wastewater treatment in the future. PMID:24657369

  17. Cyanobacterial reuse of extracellular organic carbon in microbial mats.

    PubMed

    Stuart, Rhona K; Mayali, Xavier; Lee, Jackson Z; Craig Everroad, R; Hwang, Mona; Bebout, Brad M; Weber, Peter K; Pett-Ridge, Jennifer; Thelen, Michael P

    2016-05-01

    Cyanobacterial organic matter excretion is crucial to carbon cycling in many microbial communities, but the nature and bioavailability of this C depend on unknown physiological functions. Cyanobacteria-dominated hypersaline laminated mats are a useful model ecosystem for the study of C flow in complex communities, as they use photosynthesis to sustain a more or less closed system. Although such mats have a large C reservoir in the extracellular polymeric substances (EPSs), the production and degradation of organic carbon is not well defined. To identify extracellular processes in cyanobacterial mats, we examined mats collected from Elkhorn Slough (ES) at Monterey Bay, California, for glycosyl and protein composition of the EPS. We found a prevalence of simple glucose polysaccharides containing either α or β (1,4) linkages, indicating distinct sources of glucose with differing enzymatic accessibility. Using proteomics, we identified cyanobacterial extracellular enzymes, and also detected activities that indicate a capacity for EPS degradation. In a less complex system, we characterized the EPS of a cyanobacterial isolate from ES, ESFC-1, and found the extracellular composition of biofilms produced by this unicyanobacterial culture were similar to that of natural mats. By tracing isotopically labeled EPS into single cells of ESFC-1, we demonstrated rapid incorporation of extracellular-derived carbon. Taken together, these results indicate cyanobacteria reuse excess organic carbon, constituting a dynamic pool of extracellular resources in these mats. PMID:26495994

  18. Formation of Intermediate Carbon Phases in Hydrothermal Abiotic Organic Synthesis

    NASA Astrophysics Data System (ADS)

    Fu, Q.; Foustoukos, D. I.; Seyfried, W. E.

    2005-12-01

    With high dissolved concentrations of methane and other hydrocarbon species revealed at the Rainbow and Logatchev vent systems on the Mid-Atlantic Ridge, it is essential to better understand reaction pathways of abiotic organic synthesis in hydrothermal systems. Thus, we performed a hydrothermal carbon reduction experiment with 13C labeled carbon source at temperature and pressure conditions that approximate those inferred for ultramafic-hosted hydrothermal systems. Pentlandite, a common alteration mineral phase in subseafloor reaction zones, acted as a potential catalyst. Surface analysis techniques (XPS and ToF-SIMS) were used to characterize intermediate carbon species within this process. Time series dissolved H2 and H2S concentrations indicated thermodynamic equilibrium. Dissolved H2 and H2S concentrations of 13 and 2 mmol/kg, respectively, are approximately equivalent to measured values in Rainbow and Logatchev hydrothermal systems. Isotopically pure 13C methane and other alkane species (C2H6 and C3H8) were observed throughout the experiment, and attained steady state conditions. XPS analysis on mineral product surface indicated carbon enrichment on mineral surface following reaction. The majority of surface carbon involves species containing C-C or C-H bonds, such as alkyl or methylene groups. Alcohol and carboxyl groups in fewer amounts were also observed. ToF-SIMS analysis, which can offer isotope identification with high mass resolution, showed that most of these carbon species were 13C-labeled. Unlike gas phase Fischer-Tropsch synthesis, no carbide was observed on mineral product surface during the experiment. Therefore, a reaction pathway is proposed for formation of dissolved linear alkane species in hydrothermal abiotic organic synthesis, where oxygen-bearing organic compounds are expected to form in aqueous products by way of alcohol and carboxyl groups on mineral catalyst surface.

  19. Organic farming and soil carbon sequestration: what do we really know about the benefits?

    PubMed

    Leifeld, Jens; Fuhrer, Jürg

    2010-12-01

    Organic farming is believed to improve soil fertility by enhancing soil organic matter (SOM) contents. An important co-benefit would be the sequestration of carbon from atmospheric CO2. Such a positive effect has been suggested based on data from field experiments though many studies were not designed to address the issue of carbon sequestration. The aim of our study was to examine published data in order to identify possible flaws such as missing a proper baseline, carbon mass measurements, or lack of a clear distinction between conventional and organic farming practices, thereby attributing effects of specific practices to organic farming, which are not uniquely organic. A total of 68 data sets were analyzed from 32 peer-reviewed publications aiming to compare conventional with organic farming. The analysis revealed that after conversion, soil C content (SOC) in organic systems increased annually by 2.2% on average, whereas in conventional systems SOC did not change significantly. The majority of publications reported SOC concentrations rather than amounts thus neglecting possible changes in soil bulk density. 34 out of 68 data sets missed a true control with well-defined starting conditions. In 37 out of 50 cases, the amount of organic fertilizer in the organic system exceeded that applied in the compared conventional system, and in half of the cases crop rotations differed between systems. In the few studies where crop rotation and organic fertilization were comparable in both systems no consistent difference in SOC was found. From this data analysis, we conclude that the claim for beneficial effects of organic farming on SOC is premature and that reported advantages of organic farming for SOC are largely determined by higher and often disproportionate application of organic fertilizer compared to conventional farming. PMID:21141778

  20. Determining organic pollutants in automotive industry sludge.

    PubMed

    Munaretto, Juliana S; Wonghon, Audrey L; von Mühlen, Carin

    2012-12-01

    In Brazil, the policy for disposing industrial sludge is changing from an emphasis on using controlled landfills to other treatment or co-processing methods; however, the monitoring of organic pollutants is not mandatory. The present study evaluated two general screening methods for organic pollutants in sludge generated in an automotive industrial complex in southern Brazil. The screening was performed using Soxhlet and sonication extractions and Gas Chromatograph coupled with Quadrupole Mass Spectrometry (GC/qMS). It was concluded that both techniques were effective and that most of the compounds identified were alkanes, phenols and esters. Important pollutants were detected in the sludge, which confirms the necessity of monitoring this type of residue. PMID:23007373

  1. Chemical and carbon isotopic composition of dissolved organic carbon in a regional confined methanogenic aquifer

    USGS Publications Warehouse

    Aravena, R.; Wassenaar, L.I.; Spiker, E. C.

    2004-01-01

    This study demonstrates the advantage of a combined use of chemical and isotopic tools to understand the dissolved organic carbon (DOC) cycle in a regional confined methanogenic aquifer. DOC concentration and carbon isotopic data demonstrate that the soil zone is a primary carbon source of groundwater DOC in areas close to recharge zones. An in-situ DOC source linked to organic rich sediments present in the aquifer matrix is controlling the DOC pool in the central part of the groundwater flow system. DOC fractions, 13C-NMR on fulvic acids and 14C data on DOC and CH4 support the hypothesis that the in-situ DOC source is a terrestrial organic matter and discard the Ordovician bedrock as a source of DOC. ?? 2004 Taylor and Francis Ltd.

  2. Potential responses of soil organic carbon to global environmental change

    PubMed Central

    Trumbore, Susan E.

    1997-01-01

    Recent improvements in our understanding of the dynamics of soil carbon have shown that 20–40% of the approximately 1,500 Pg of C stored as organic matter in the upper meter of soils has turnover times of centuries or less. This fast-cycling organic matter is largely comprised of undecomposed plant material and hydrolyzable components associated with mineral surfaces. Turnover times of fast-cycling carbon vary with climate and vegetation, and range from <20 years at low latitudes to >60 years at high latitudes. The amount and turnover time of C in passive soil carbon pools (organic matter strongly stabilized on mineral surfaces with turnover times of millennia and longer) depend on factors like soil maturity and mineralogy, which, in turn, reflect long-term climate conditions. Transient sources or sinks in terrestrial carbon pools result from the time lag between photosynthetic uptake of CO2 by plants and the subsequent return of C to the atmosphere through plant, heterotrophic, and microbial respiration. Differential responses of primary production and respiration to climate change or ecosystem fertilization have the potential to cause significant interrannual to decadal imbalances in terrestrial C storage and release. Rates of carbon storage and release in recently disturbed ecosystems can be much larger than rates in more mature ecosystems. Changes in disturbance frequency and regime resulting from future climate change may be more important than equilibrium responses in determining the carbon balance of terrestrial ecosystems. PMID:11607735

  3. Modeling stable isotope and organic carbon in hillslope stormflow

    NASA Astrophysics Data System (ADS)

    Dusek, Jaromir; Vogel, Tomas; Dohnal, Michal; Marx, Anne; Jankovec, Jakub; Sanda, Martin; Votrubova, Jana; Barth, Johannes A. C.; Cislerova, Milena

    2016-04-01

    Reliable prediction of water movement and fluxes of dissolved substances (such as stable isotopes and organic carbon) at both the hillslope and the catchment scales remains a challenge due to complex boundary conditions and soil spatial heterogeneity. In addition, microbially mediated transformations of dissolved organic carbon (DOC) are known to affect balance of DOC in soils, hence the transformations need to be included in a conceptual model of a DOC transport. So far, only few studies utilized stable isotope information in modeling and even fewer linked dissolved carbon fluxes to mixing and/or transport models. In this study, stormflow dynamics of oxygen-18 isotope and dissolved organic carbon was analyzed using a physically based modeling approach. One-dimensional dual-continuum vertical flow and transport model, based on Richards and advection-dispersion equations, was used to simulate the subsurface transport processes in a forest soil during several observed rainfall-runoff episodes. The transport of heat in the soil profile was described by conduction-advection equation. Water flow and transport of solutes and heat were assumed to take place in two mutually communicating porous domains, the soil matrix and the network of preferential pathways. The rate of microbial transformations of DOC was assumed to depend on soil water content and soil temperature. Oxygen-18 and dissolved organic carbon concentrations were observed in soil pore water, hillslope stormflow (collected in the experimental hillslope trench), and stream discharge (at the catchment outlet). The modeling was used to analyze the transformation of input solute signals into output hillslope signals observed in the trench stormflow. Signatures of oxygen-18 isotope in hillslope stormflow as well as isotope concentration in soil pore water were predicted reasonably well. Due to complex nature of microbial transformations, prediction of DOC rate and transport was associated with a high uncertainty.

  4. An Idealized Model of Organic Carbon Dynamics on the Continental Margin of the Eastern United States

    NASA Astrophysics Data System (ADS)

    Siedlecki, S. A.; Archer, D.; Mahadevan, A.

    2003-12-01

    Continental margins play a significant role in the production and burial of organic carbon in the ocean, bur these areas are poorly resolved global circulation models. In this study, a high-resolution three-dimensional, nonhydrostatic model of an idealized eastern coastal United States after Mahadevan and Archer, 1998, was modified to simulate organic carbon production and export off the shelf. The model assumes a periodic north and south boundary, and an offshore boundary at the shelf-break density front determined by bathymetry. The model uses a free surface and a sigma grid in the vertical. The model is initialized with a vertical nutrient profile taken from the open Atlantic Ocean. As the winds are given time to influence the region, upwelling conditions can result in the vertical movement of water. Vertical diffusion also carries nutrients into the euphotic zone. Excess nutrients in the euphotic zone are converted to particles that advect with the flow while sinking with a velocity of 10-5 m/s. Remineralization is treated as a first-order decay. We will vary the alongshore wind stress, shelf width, and vertical diffusivity to determine their respective impacts on organic carbon export. Eventually, we hope to parameterize the impact of coastal circulation on the carbon cycle with global circulation and carbon models. Mahadevan, A., Archer, D., Modeling a Limited Region of the Ocean, Journal of Computational Physics 145, 555-574, 1998.

  5. Removal of organic impurities from liquid carbon dioxide

    NASA Astrophysics Data System (ADS)

    Zito, Richard R.

    2002-09-01

    The use of a high velocity stream of carbon dioxide snowflakes to clean large optics is well known, and has gained widespread acceptance in the astronomical community as a telescope maintenance technique. Ultimately, however, the success of carbon dioxide snow cleaning depends on the availability of high purity carbon dioxide. The higher the purity of the carbon dioxide, the longer will be the time interval between required mirror washings. The highest grades of commercially produced liquid carbon dioxide are often not available in the more remote regions of the world - such as where major astronomical observatories are often located. Furthermore, the purity of even the highest grades of carbon dioxide are only nominal, and wide variations are known to occur from tank to tank. Occasionally, visible deposits of organic impurities are left behind during cleaning with carbon dioxide that is believed to be 99.999% pure. A zeolite molecular sieve based filtration system has proven to be very effective in removing these organic impurities. A zeolite is a complex alumino-silicate. One example has an empirical formula of Na2O(Al2O3)(SiO2)2yH2O, where y=0 to 8. The zeolites have an open crystal structure and are capable of trapping impurities like 8-methylheptadecane (an oil) and 2,6-octadine-1-ol,3,7- dimethyl-,(E)- (a fatty acid). In fact, a zeolite can trap 29.5% of its own weight in SAE 20 lubricant at 25 degree(s)C. After filtration of liquid CO2 through zeolites, the concentration of measured impurities was below the detection limit for state-of-the-art gas chromatography systems.

  6. Determination of organic-matter content of Appalachian Devonian shales from gamma-ray logs.

    USGS Publications Warehouse

    Schmoker, J.W.

    1981-01-01

    The organic-matter content of the Devonian shale of the Appalachian basin is important for assessing natural-gas resources. In most of the western part of the Appalachian basin the organic-matter content of the Devonian shale can be estimated from gamma-ray wire-line logs. Organic-matter contents estimated using these logs are compared with determinations from direct laboratory analyses of organic carbon for 74 intervals of varying thickness from 12 widely separated wells. The cumulative pool of gamma-ray logs for the Devonian shale forms a large and geographically broad data base. The approach may also be applicable to other formations.-from Author

  7. Determination of polar organic solutes in oil-shale retort water

    USGS Publications Warehouse

    Leenheer, J.A.; Noyes, T.I.; Stuber, H.A.

    1982-01-01

    A variety of analytical methods were used to quantitatively determine polar organic solutes in process retort water and a gas-condensate retort water produced in a modified in situ oil-shale retort. Specific compounds accounting for 50% of the dissolved organic carbon were identified in both retort waters. In the process water, 42% of the dissolved organic carbon consisted of a homologous series of fatty acids from C2 to C10. Dissolved organic carbon percentages for other identified compound classes were as follows: aliphatic dicarboxylic acids, 1.4%; phenols, 2.2%; hydroxypyridines, 1.1%; aliphatic amides, 1.2%. In the gas-condensate retort water, aromatic amines were most abundant at 19.3% of the dissolved organic carbon, followed by phenols (17.8%), nitriles (4.3%), aliphatic alcohols (3.5%), aliphatic ketones (2.4%), and lactones (1.3%). Steam-volatile organic solutes were enriched in the gas-condensate retort water, whereas nonvolatile acids and polyfunctional neutral compounds were predominant organic constituents of the process retort water.

  8. Saltwater intrusion into tidal freshwater marshes alters the biogeochemical processing of organic carbon

    NASA Astrophysics Data System (ADS)

    Neubauer, S. C.; Franklin, R. B.; Berrier, D. J.

    2013-12-01

    Environmental perturbations in wetlands affect the integrated plant-microbial-soil system, causing biogeochemical responses that can manifest at local to global scales. The objective of this study was to determine how saltwater intrusion affects carbon mineralization and greenhouse gas production in coastal wetlands. Working with tidal freshwater marsh soils that had experienced ~ 3.5 yr of in situ saltwater additions, we quantified changes in soil properties, measured extracellular enzyme activity associated with organic matter breakdown, and determined potential rates of anaerobic carbon dioxide (CO2) and methane (CH4) production. Soils from the field plots treated with brackish water had lower carbon content and higher C : N ratios than soils from freshwater plots, indicating that saltwater intrusion reduced carbon availability and increased organic matter recalcitrance. This was reflected in reduced activities of enzymes associated with the hydrolysis of cellulose and the oxidation of lignin, leading to reduced rates of soil CO2 and CH4 production. The effects of long-term saltwater additions contrasted with the effects of short-term exposure to brackish water during three-day laboratory incubations, which increased rates of CO2 production but lowered rates of CH4 production. Collectively, our data suggest that the long-term effect of saltwater intrusion on soil CO2 production is indirect, mediated through the effects of elevated salinity on the quantity and quality of autochthonous organic matter inputs to the soil. In contrast, salinity, organic matter content, and enzyme activities directly influence CH4 production. Our analyses demonstrate that saltwater intrusion into tidal freshwater marshes affects the entire process of carbon mineralization, from the availability of organic carbon through its terminal metabolism to CO2 and/or CH4, and illustrate that long-term shifts in biogeochemical functioning are not necessarily consistent with short

  9. Saltwater intrusion into tidal freshwater marshes alters the biogeochemical processing of organic carbon

    NASA Astrophysics Data System (ADS)

    Neubauer, S. C.; Franklin, R. B.; Berrier, D. J.

    2013-07-01

    Environmental perturbations in wetlands affect the integrated plant-microbial-soil system, causing biogeochemical responses that can manifest at local to global scales. The objective of this study was to determine how saltwater intrusion affects carbon mineralization and greenhouse gas production in coastal wetlands. Working with tidal freshwater marsh soils that had experienced roughly 3.5 yr of in situ saltwater additions, we quantified changes in soil properties, measured extracellular enzyme activity associated with organic matter breakdown, and determined potential rates of anaerobic carbon dioxide (CO2) and methane (CH4) production. Soils from the field plots treated with brackish water had lower carbon content and higher C : N ratios than soils from freshwater plots, indicating that saltwater intrusion reduced carbon availability and increased organic matter recalcitrance. This was reflected in reduced activities of enzymes associated with the hydrolysis of cellulose and the oxidation of lignin, leading to reduced rates of soil CO2 and CH4 production. The effects of long-term saltwater additions contrasted with the effects of short-term exposure to brackish water during three-day laboratory incubations, which increased rates of CO2 production but lowered rates of CH4 production. Collectively, our data suggest that the long-term effect of saltwater intrusion on soil CO2 production is indirect, mediated through the effects of elevated salinity on the quantity and quality of autochthonous organic matter inputs to the soil. In contrast, salinity, organic matter content, and enzyme activities directly influence CH4 production. Our analyses demonstrate that saltwater intrusion into tidal freshwater marshes affects the entire process of carbon mineralization, from the availability of organic carbon through its terminal metabolism to CO2 and/or CH4, and illustrate that long-term shifts in biogeochemical functioning are not necessarily consistent with short

  10. The Decomposition of Carbonates and Organics on Mars

    NASA Technical Reports Server (NTRS)

    Quinn, Richard C.; Zent, Aaron; McKay, Chris; DeVincenzi, Donald L. (Technical Monitor)

    2000-01-01

    The return and analysis of pristine material that is relict of a putative period of chemical evolution is a fumdamental goal of the exobiological exploration of Mars. In order to accomplish this objective, it is desirable to find oxidant-free regions where pristine material can be accessed at the shallowest possible depth (ideally directly from the surface). The objective of our ongoing research is to understand the spatial and temporal distribution of oxidants in the martian regolith and the redox chemistry of the soil; in effect to understand the chemical mechanisms and kinetics relating to the in-situ destruction of organics and the formation of the reactive species responsible for the Viking biology results. In this work, we report on experimental studies of oxidizing processes that may contribute to carbonate and organic degradation on Mars. Organic molecules directly exposed to solar UV may decomposed either directly into CO2, or into more volatile organic fragments. Organic macromolecules not directly exposed to high UV flux are most likely to be affected by atmospheric oxidants which can diffuse to their surfaces. The oxidizing processes examined include: gas-phase oxidants, UV photolysis, and UV-assisted heterogeneous catalysis. For example, assuming a meteroritic infall rate of 4 x 10(exp -4) g/m^2yr (Flynn and McKay 1990) and a flux of organic carbon of 2 x 10(exp -5) g/m^2yr, laboratory measurements of the UV-assisted decomposition of benzenehexacarboxylic acid (mellitic acid, a likely intermediate of kerogen oxidation), indicate its decomposition rate on Mars would exceed the total flux of organic carbon to the planet by over four orders of magnitude. Our measurements indicate that although the decomposition temperature of kerogens in some cases exceeds the temperature limit of the Viking GCMS, it is unlikely kerogens or their decomposition intermediates were present at the Viking landings sites at levels above the GCMS detection limits.

  11. Detailed Carbon Isotopic Characterization of Aerosol-Derived Organic Carbon Deposited to two Temperate Watersheds

    NASA Astrophysics Data System (ADS)

    Wozniak, A. S.; Bauer, J. E.; Keesee, E. E.; McNichol, A. P.; Xu, L.; Dickhut, R. M.

    2008-12-01

    Atmospheric deposition of carbonaceous aerosols can be a quantitatively significant flux in the carbon budgets of temperate watersheds. Characterizing the sources and fates of this material is therefore critical for assessing its role in carbon and organic matter cycling in these systems. Aerosol samples were collected in the Hudson and York River watersheds throughout 2006-2007 and analyzed for quantities and isotopic signatures (δ13C, Δ14C) of total and water-soluble organic carbon (TOC, WSOC, respectively). On average ~2.4 and 2.1 mg m-2 d-1 of aerosol TOC were deposited to the Hudson and York River watersheds, respectively, and nearly half of this material was water-soluble. δ13C analyses indicated that both the TOC and the WSOC were primarily terrestrial in nature. TOC Δ14C signatures covered a broad range for both watersheds, with calculated contributions from fossil sources (e.g., anthropogenic combustion of petroleum, coal, etc.) ranging from 0% for samples collected during the summer of 2007 to approximately 50% for samples collected in the winter of 2007. Aerosol-derived WSOC Δ14C values were less variable and were nearly always enriched in 14C with respect to the corresponding TOC, indicating that contemporary aerosol material tends to partition into the aqueous phase, while fossil-derived aerosol OC is more likely to remain insoluble. However, WSOC still often showed considerable contributions from fossil OC (up to 20%). Thus, some portion of the anthropogenic fossil-derived aerosol OC is relatively soluble and may be transported hydrologically through watersheds and aquatic systems. A subset of aerosol samples from each watershed was selected for more thorough isotopic analysis of operationally-defined components of the carbonaceous material. Isotopic signatures were obtained for TOC, WSOC, total solvent-extract, and the aliphatic, aromatic, and polar components. Isotopic information on these fractions allows us to determine which components

  12. Retardation of volatile organic compounds in ground water in low organic carbon sediments

    SciTech Connect

    Hoffman, F.

    1995-04-01

    It is postulated that adsorption onto aquifer matrix surfaces is only one of the processes that retard contaminants in ground water in unconsolidated sediments; others include hydrodynamic dispersion, abiotic/biotic degradation, matrix diffusion, partitioning to organic carbon, diffusion into and retention in dead-end pores, etc. This work aims at these processes in defining the K{sub d} of VOCs in sediments with low organic carbon content. Experiments performed include an initial column experiment for VOC (TCE and perchloroethylene(PCE)) retardation tests on geological materials, PCE and TCE data from LLNL sediments, and a preliminary multilayer sampler experiment. The VOC K{sub d}s in low organic carbon permeable aquifer materials are dependent on the VOC composition and independent of aquifer grain size, indicating that sorption was not operative and that the primary retarding factors are diffusion controlled. The program of future experiments is described.

  13. Soil organic carbon stocks and fluxes due to land use conversions at the European scale

    NASA Astrophysics Data System (ADS)

    Gobin, A.; Campling, P.

    2012-04-01

    (HOC) assimilated depends on the yields, as these directly relate to potential residue production, and on the prevailing climate with cold temperatures and dry moisture regimes being less favourable. Incorporating all crop residues into the soil results in HOC fluxes that range from 1.36 tonnes HOC/ha for oilseed and 1.14 tonnes HOC/ha for cereal to 0.54 tonnes/ha for sugar beet. The HOC fluxes drop to 0.69, 0.58 and 0.05 tonnes HOC/ha respectively when all residues are removed, e.g. for bio-energy purposes. Taking into account the projected areas for cereals (65 Mha), oilseed (10 Mha) and sugarbeet (2 Mha) in 2030, shows that residue management of cereals has a much larger impact on carbon fluxes to the agricultural soil than oilseed and sugar beet. The removal of all crop residues result in a lowering of soil organic carbon stocks, a reduction of humified organic carbon fluxes into the soil and an increase of carbon dioxide concentrations in the atmosphere. A significant minimum percentage of crop residues should be retained in the soils. Land management, land use changes and climate change have a significant influence on soil organic carbon stocks and fluxes across the EU-27. Determining the soil sequestration potential necessitates soil monitoring to provide evidence on the state of, and change, in agricultural soils, allowing to evaluate its effectiveness.

  14. Organic carbon and nitrogen content associated with colloids and suspended particulates from the Mississippi River and some of its tributaries

    USGS Publications Warehouse

    Rostad, C.E.; Leenheer, J.A.; Daniel, S.R.

    1997-01-01

    Suspended material samples were collected at 16 sites along the Mississippi River and some of its tributaries during July-August 1991, October-November 1991, and April-May 1992, and separated into colloid and particulate fractions to determine the organic carbon content of these two fractions of suspended material. Sample collection involved centrifugation to isolate the suspended particulate fraction and ultrafiltration to isolate the colloid fraction. For the first time, particulate and colloid concentrations and organic carbon and nitrogen content were investigated along the entire reach of the Mississippi River from above Minneapolis, Minnesota, to below New Orleans, Louisiana. Organic carbon content of the colloid (15.2 percent) was much higher than organic carbon content of the particulate material (4.8 percent). Carbon/nitrogen ratios of colloid and particulate phases were more similar to ratios for microorganisms than to ratios for soils, humic materials, or plants.Suspended material samples were collected at 16 sites along the Mississippi River and some of its tributaries during July-August 1991, October-November 1991, and April-May 1992, and separated into colloid and particulate fractions to determine the organic carbon content of these two fractions of suspended material. Sample collection involved centrifugation to isolate the suspended particulate fraction and ultrafiltration to isolate the colloid fraction. For the first time, particulate and colloid concentrations and organic carbon and nitrogen content were investigated along the entire reach of the Mississippi River from above Minneapolis, Minnesota, to below New Orleans, Louisiana. Organic carbon content of the colloid (15.2 percent) was much higher than organic carbon content of the particulate material (4.8 percent). Carbon/nitrogen ratios of colloid and particulate phases were more similar to ratios for microorganisms than to ratios for soils, humic materials, or plants.

  15. Soil organic carbon pools in olive groves of different age

    NASA Astrophysics Data System (ADS)

    Massaccesi, Luisa; De Feudis, Mauro; Nasini, Luigi; Regni, Luca; D'Ascoli, Rosaria; Castaldi, Simona; Proietti, Primo; Agnelli, Alberto

    2016-04-01

    In the last years, the practices which favor the increase of soil organic carbon in the agroecosystem have been widely studied because of their influence on the reduction of atmospheric CO2 (Lal, 1993; Schlesinger, 2000). The accumulation of the organic carbon into the soil depends to a great extent upon climate and pedological properties (Burke et al., 1989; Miller et al., 1994), although in the agricultural soils the cultivation system also plays a key role. The olive grove might potentially represent a relevant land use to improve C sequestration in soil, but there are few data available to support this hypothesis. In a study site located in central Italy (Deruta, PG), we analyzed the soil organic carbon (SOC) pools in two olive groves of different age (7 and 30 years) and, as control, in a site adjacent to the groves cropped with cereals for at least 30 years. With the aim to isolate and quantify the active, intermediate and passive functional SOC pools in the olive groves and in the control, we used a combined physical and chemical fractionation method (Zimmermann et al., 2007). The main results shown that the total organic carbon content in the Ap horizons was the highest in the 30-years-old olive grove, followed by the 7-years-old olive grove, and then by the control soil. The content of active C, in form of particulate organic matter (POM) and water soluble organic matter (WEOM), was greater in the olive grove compared to the control soil and increase with the age of the grove. About the amount of C in the intermediate and passive pools, no significant differences were found among the olive groves and the control. These preliminary results indicated that the greater total organic C content occurred in the 30-year-old olive grove with respect to the 7-years-old grove and the control, has to be ascribed to the greater content of active organic matter (POM and WEOM), and not to the accumulation in soil of organic C in a more stabilised form.

  16. Carbon content of common airborne fungal species and fungal contribution to aerosol organic carbon in a subtropical city

    NASA Astrophysics Data System (ADS)

    Cheng, Jessica Y. W.; Chan, Chak K.; Lee, C.-T.; Lau, Arthur P. S.

    Interest in the role and contribution of fungi to atmospheric aerosols and processes grows in the past decade. Substantial data or information such as fungal mass or carbon loading to ambient aerosols is however still lacking. This study aimed to quantify the specific organic carbon content (OC per spore) of eleven fungal species commonly found airborne in the subtropics, and estimated their contribution to organic carbon in aerosols. The specific OC contents showed a size-dependent relationship ( r = 0.64, p < 0.05) and ranged from 3.6 to 201.0 pg carbon per spore or yeast cell, giving an average of 6.0 pg carbon per spore (RSD 51%) for spore or cell size less than 10 μm. In accounting for natural variations in the composition and abundance of fungal population, weighted-average carbon content for field samples was adopted using the laboratory determined specific OC values. An average of 5.97 pg carbon per spore (RSD 3.8%) was enumerated from 28 field samples collected at the university campus. The mean fungal OC concentration was 3.7, 6.0 and 9.7 ng m -3 in PM 2.5, PM 2.5-10 and PM 10, respectively. These corresponded to 0.1%, 1.2% and 0.2% of the total OC in PM 2.5, PM 2.5-10 and PM 10, respectively. In the study period, rain provided periods with low total OC but high fungal prevalence and fungi contributed 7-32% OC in PM 2.5-10 or 2.4-7.1% OC in PM 10. More extensive studies are deserved to better understand the spatial-, temporal- and episodic dependency on the fungal OC contribution to the atmospheric aerosols.

  17. Mineralization of allochthonous organic carbon in lake sediments, from lake to landscape scale

    NASA Astrophysics Data System (ADS)

    Gudasz, C.; Ask, J.; Tranvik, L. J.; Karlsson, J.

    2012-04-01

    Lake sediments are well-recognized sites for the processing as well as sequestration of organic carbon. In particular boreal lake sediments have been recognized as important sites for the sequestration of organic carbon, comparable to soils or living biomass. Lakes in the boreal zone import large amounts of terrestrially derived organic carbon. Part of this organic carbon reaches the sediment surface through flocculation and sedimentation. The microbial processing of organic carbon represents one of the main factors that regulate the balance between sequestration of organic carbon and emission of green house gasses in boreal lake sediments. Recently, it has been shown a strong constrained microbial processing of allochthonous organic carbon in boreal lake sediments. However, a clear picture about the extent of the allochthonous organic carbon influence on the mineralization of sediment organic carbon in lakes and its significance at a large scale is currently lacking. We conducted a study, which explored the effect of allochthonous organic carbon on sediment organic carbon mineralization along a gradient of lakes characterized by increasing terrestrial organic carbon influence. We show a strong negative effect on sediment mineralization in lakes with increasing allochthonous organic carbon influence, which applies to a large number of lakes in the boreal zone.

  18. Dissolved Organic Carbon in Headwater Streams and Riparian Soil Organic Carbon along an Altitudinal Gradient in the Wuyi Mountains, China

    PubMed Central

    Huang, Wei; McDowell, William H.; Zou, Xiaoming; Ruan, Honghua; Wang, Jiashe; Li, Liguang

    2013-01-01

    Stream water dissolved organic carbon (DOC) correlates positively with soil organic carbon (SOC) in many biomes. Does this relationship hold in a small geographic region when variations of temperature, precipitation and vegetation are driven by a significant altitudinal gradient? We examined the spatial connectivity between concentrations of DOC in headwater stream and contents of riparian SOC and water-soluble soil organic carbon (WSOC), riparian soil C:N ratio, and temperature in four vegetation types along an altitudinal gradient in the Wuyi Mountains, China. Our analyses showed that annual mean concentrations of headwater stream DOC were lower in alpine meadow (AM) than in subtropical evergreen broadleaf forest (EBF), coniferous forest (CF), and subalpine dwarf forest (SDF). Headwater stream DOC concentrations were negatively correlated with riparian SOC as well as WSOC contents, and were unrelated to riparian soil C:N ratio. Our findings suggest that DOC concentrations in headwater streams are affected by different factors at regional and local scales. The dilution effect of higher precipitation and adsorption of soil DOC to higher soil clay plus silt content at higher elevation may play an important role in causing lower DOC concentrations in AM stream of the Wuyi Mountains. Our results suggest that upscaling and downscaling of the drivers of DOC export from forested watersheds when exploring the response of carbon flux to climatic change or other drivers must done with caution. PMID:24265737

  19. Dissolved organic carbon in headwater streams and riparian soil organic carbon along an altitudinal gradient in the Wuyi Mountains, China.

    PubMed

    Huang, Wei; McDowell, William H; Zou, Xiaoming; Ruan, Honghua; Wang, Jiashe; Li, Liguang

    2013-01-01

    Stream water dissolved organic carbon (DOC) correlates positively with soil organic carbon (SOC) in many biomes. Does this relationship hold in a small geographic region when variations of temperature, precipitation and vegetation are driven by a significant altitudinal gradient? We examined the spatial connectivity between concentrations of DOC in headwater stream and contents of riparian SOC and water-soluble soil organic carbon (WSOC), riparian soil C:N ratio, and temperature in four vegetation types along an altitudinal gradient in the Wuyi Mountains, China. Our analyses showed that annual mean concentrations of headwater stream DOC were lower in alpine meadow (AM) than in subtropical evergreen broadleaf forest (EBF), coniferous forest (CF), and subalpine dwarf forest (SDF). Headwater stream DOC concentrations were negatively correlated with riparian SOC as well as WSOC contents, and were unrelated to riparian soil C:N ratio. Our findings suggest that DOC concentrations in headwater streams are affected by different factors at regional and local scales. The dilution effect of higher precipitation and adsorption of soil DOC to higher soil clay plus silt content at higher elevation may play an important role in causing lower DOC concentrations in AM stream of the Wuyi Mountains. Our results suggest that upscaling and downscaling of the drivers of DOC export from forested watersheds when exploring the response of carbon flux to climatic change or other drivers must done with caution. PMID:24265737

  20. Erosion of Organic Carbon from Permafrost Zones in the Arctic as a Geological Carbon Dioxide Sink

    NASA Astrophysics Data System (ADS)

    Hilton, R. G.; Galy, V.; Gaillardet, J.; Dellinger, M.; Bryant, C.; O'Regan, M.; Gröcke, D. R.; Coxall, H.; Bouchez, J.; Calmels, D.

    2015-12-01

    Soils of the northern high latitudes store carbon over millennial timescales and contain almost double the carbon stock of the atmosphere. The exposure and decomposition of aged organic matter in these soils is a carbon dioxide (CO2) source to the atmosphere. Permafrost thaw over the coming century may result in a significant CO2 release. However, some of this soil organic carbon in permafrost zones can be eroded and input to rivers. If it escapes degradation during river transport and is buried in ocean sediments, it instead contributes to a longer-term (>104 yr), geological CO2sink. Despite this recognition, the erosional flux and fate of particulate organic carbon (POC) in large rivers draining permafrost zones remains poorly constrained. We quantify POC source, flux and fate in the Mackenzie River Basin, the main sediment supplier to the Arctic Ocean, using radiocarbon, stable carbon isotopes and element ratios to correct for rock-derived POC. The eroded biospheric POC has resided in the basin for millennia, with a mean radiocarbon age of 5800±800 yr. Rivers eroding continuous permafrost zones contribute the oldest biospheric POC. Based on the measured biospheric POC content and annual sediment flux, we calculate a biospheric POC flux of 2.2 (+1.3/-0.9) TgC yr-1 from the Mackenzie River to the Arctic Ocean, three times the CO2 drawdown by silicate weathering. Offshore we find evidence for efficient terrestrial carbon burial over the Holocene period. Our findings demonstrate how erosion of organic carbon-rich, high latitude soils can result in a significant geological CO2sink. We postulate that this geological CO2 sink is sensitive to climate conditions in the Arctic. The transfer can operate when high latitudes host carbon stocks in soil, and while rivers can erode and transfer sediments to the Arctic Ocean. Over the last 1Ma, the erosional transfer was likely to have been enhanced during interglacials. We propose that erosion of biospheric carbon by large

  1. Enhanced top soil carbon stocks under organic farming

    PubMed Central

    Gattinger, Andreas; Muller, Adrian; Haeni, Matthias; Skinner, Colin; Fliessbach, Andreas; Buchmann, Nina; Mäder, Paul; Stolze, Matthias; Smith, Pete; Scialabba, Nadia El-Hage; Niggli, Urs

    2012-01-01

    It has been suggested that conversion to organic farming contributes to soil carbon sequestration, but until now a comprehensive quantitative assessment has been lacking. Therefore, datasets from 74 studies from pairwise comparisons of organic vs. nonorganic farming systems were subjected to metaanalysis to identify differences in soil organic carbon (SOC). We found significant differences and higher values for organically farmed soils of 0.18 ± 0.06% points (mean ± 95% confidence interval) for SOC concentrations, 3.50 ± 1.08 Mg C ha−1 for stocks, and 0.45 ± 0.21 Mg C ha−1 y−1 for sequestration rates compared with nonorganic management. Metaregression did not deliver clear results on drivers, but differences in external C inputs and crop rotations seemed important. Restricting the analysis to zero net input organic systems and retaining only the datasets with highest data quality (measured soil bulk densities and external C and N inputs), the mean difference in SOC stocks between the farming systems was still significant (1.98 ± 1.50 Mg C ha−1), whereas the difference in sequestration rates became insignificant (0.07 ± 0.08 Mg C ha−1 y−1). Analyzing zero net input systems for all data without this quality requirement revealed significant, positive differences in SOC concentrations and stocks (0.13 ± 0.09% points and 2.16 ± 1.65 Mg C ha−1, respectively) and insignificant differences for sequestration rates (0.27 ± 0.37 Mg C ha−1 y−1). The data mainly cover top soil and temperate zones, whereas only few data from tropical regions and subsoil horizons exist. Summarizing, this study shows that organic farming has the potential to accumulate soil carbon. PMID:23071312

  2. 42 CFR 422.570 - Expediting certain organization determinations.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... responsible for making the determination, as directed by the MA organization. (2) A physician may provide oral... an expedited determination if it determines that applying the standard timeframe for making a... expedited determination if the physician indicates that applying the standard timeframe for making...

  3. Ancient Organic Matter Sources to the Hudson-Mohawk River System: Implications of Riverine Transport of Ancient Organic Matter for the Global Biogeochemical Carbon Cycle

    NASA Astrophysics Data System (ADS)

    Longworth, B. E.; Petsch, S. T.; Raymond, P. A.

    2003-12-01

    The connection between erosion of rocks on the continents and deposition of marine sediments is riverine transport. Rivers are an important component of both the contemporary and long-term geologic carbon cycles. They erode ancient organic matter [OM] buried in sedimentary rock, carbon stored in soils, and carbonate bearing rock. Current understanding is that ancient OM is chemically and biologically reactive during weathering and riverine transport. However, while much OM exposed during weathering and transport is oxidized to CO2, a significant portion is not remineralized, but instead is delivered downstream and reburied in marine sediments. This riverine conduit potentially allows ancient organic carbon to remain chemically distinct from pools of the contemporary carbon cycle. If a significant portion of ancient organic carbon remains sequestered in reduced form via this mechanism, there are important implications for the global carbon cycle over geologic time. These include carbon isotope effects, reservoir sizes and turnover rates, and ultimately, the composition of earth's atmosphere over geologic time. The Ordovician and Devonian shales of the Hudson-Mohawk watershed in upstate New York, USA, provide an ideal location to study the behavior of OM in a river system. In this study, we quantify sources of the dissolved and particulate organic carbon load of headwater streams draining these organic rich black shales using isotopic and molecular tracers of organic matter source. These tracers include stable isotopes of carbon and nitrogen, radiocarbon isotope ratios, and chromatographic signatures produced by pyrolysis-GC. We employ a GIS-based matrix of field sites in watersheds of contrasting lithology (OM-rich shales vs. OM-free crystalline basement) and surface cover, under the assumption that the two main controls on riverine carbon under similar climatic conditions are land use and underlying rock type. Samples include stream waters as well as endmember

  4. Soil Organic Carbon Stocks in Depositional Landscapes of Bavaria

    NASA Astrophysics Data System (ADS)

    Kriegs, Stefanie; Schwindt, Daniel; Völkel, Jörg; Kögel-Knabner, Ingrid

    2016-04-01

    Erosion leads to redistribution and accumulation of soil organic matter (SOM) within agricultural landscapes. These fluvic and colluvic deposits are characterized by a highly diverse vertical structure and can contain high amounts of soil organic carbon (SOC) over the whole soil profile. Depositional landscapes are therefore not only productive sites for agricultural use but also influence carbon dynamics which is of great interest with regard on the recent climate change debate. The aim of our study is to elucidate the spatial distribution of organic carbon stocks, as well as its depth function and the role of these landscapes as a reservoir for SOM. Therefore we compare two representative depositional landscapes in Bavaria composed of different parent materials (carbonate vs. granitic). We hypothesize that the soils associated with different depositional processes (fluvial vs. colluvial) differ in SOC contents and stocks, also because of different hydromorphic regimes in fluvic versus colluvic soil profiles. Sampling sites are located in the Alpine Foreland (quaternary moraines with carbonatic parent material) and the foothills of the Bavarian Forest (Granite with Loess) with the main soil types Fluvisols, Gleysols and Luvisols. At both sites we sampled twelve soil profiles up to 150 cm depth, six in the floodplain and six along a vertical slope transect. We took undisturbed soil samples from each horizon and analyzed them for bulk density, total Carbon (OC and IC) and total Nitrogen (N) concentrations. This approach allows to calculate total OC contents and OC stocks and to investigate vertical and horizontal distribution of OC stocks. It will also reveal differences in OC stocks due to the location of the soil profile in fluvic or colluvic deposition scenarios.

  5. Determination of organic emissions from new carpeting

    SciTech Connect

    Pleil, J.D.; Whiton, R.S.

    1990-01-01

    New carpeting has been the source of a number of indoor air health and odor complaints. Investigations of a variety of carpet samples have shown that there is a diversity of organic emissions among carpet types; some of the compounds found have been listed in the NIOSH Registry of Toxic Effects of Chemical Substances. The paper describes two complementary analytical methods for screening carpet samples: a 'headspace' method for volatile emissions and a Soxhlet extraction method using methylene chloride for the semi-volatile and non-volatile compounds. The analytical results from seven carpet types are presented with special emphasis on the compound 4-phenylcyclohexene, one of the causes of 'new carpet smell,' which has also been anectdotally linked to adverse short term health effects. Other compounds of possible interest that were found include dichlorobenzene, bis(2-ethylhexyl)-phthalate, triethyl phosphate, epsilon-caprolactam, and methylene-bis(4-isocyanatobenzene).

  6. Carbon isotope fractionation of sapropelic organic matter during early diagenesis

    USGS Publications Warehouse

    Spiker, E. C.; Hatcher, P.G.

    1984-01-01

    Study of an algal, sapropelic sediment from Mangrove Lake, Bermuda shows that the mass balance of carbon and stable carbon isotopes in the major organic constituents is accounted for by a relatively straightforward model of selective preservation during diagenesis. The loss of 13C-enriched carbohydrates is the principal factor controlling the intermolecular mass balance of 13C in the sapropel. Results indicate that labile components are decomposed leaving as a residual concentrate in the sediment an insoluble humic substance that may be an original biochemical component of algae and associated bacteria. An overall decrease of up to about 4??? in the ?? 13C values of the organic matter is observed as a result of early diagenesis. ?? 1984.

  7. Dilution limits dissolved organic carbon utilization in the deep ocean

    NASA Astrophysics Data System (ADS)

    Arrieta, Jesús M.; Mayol, Eva; Hansman, Roberta L.; Herndl, Gerhard J.; Dittmar, Thorsten; Duarte, Carlos M.

    2015-04-01

    Oceanic dissolved organic carbon (DOC) is the second largest reservoir of organic carbon in the biosphere. About 72% of the global DOC inventory is stored in deep oceanic layers for years to centuries, supporting the current view that it consists of materials resistant to microbial degradation. An alternative hypothesis is that deep-water DOC consists of many different, intrinsically labile compounds at concentrations too low to compensate for the metabolic costs associated to their utilization. Here, we present experimental evidence showing that low concentrations rather than recalcitrance preclude consumption of a substantial fraction of DOC, leading to slow microbial growth in the deep ocean. These findings demonstrate an alternative mechanism for the long-term storage of labile DOC in the deep ocean, which has been hitherto largely ignored.

  8. BOREAS TGB-10 Volatile Organic Carbon Data over the SSA

    NASA Technical Reports Server (NTRS)

    Westberg, Hal; Hall, Forrest G. (Editor); Conrad, Sara K. (Editor); Hall, Brad; Jackson, Andrea V.

    2000-01-01

    The BOREAS TGB-10 team collected several trace gas data sets in its efforts to determine the role of biogenic hydrocarbon emissions with respect to boreal forest carbon cycles. This data set contains measured VOC concentrations. These data were obtained at the SSA-OJP site from May to September 1994. The data are stored in tabular ASCII files.

  9. Effects of organic carbon sequestration strategies on soil enzymatic activities

    NASA Astrophysics Data System (ADS)

    Puglisi, E.; Suciu, N.; Botteri, L.; Ferrari, T.; Coppolecchia, D.; Trevisan, M.; Piccolo, A.

    2009-04-01

    Greenhouse gases emissions can be counterbalanced with proper agronomical strategies aimed at sequestering carbon in soils. These strategies must be tested not only for their ability in reducing carbon dioxide emissions, but also for their impact on soil quality: enzymatic activities are related to main soil ecological quality, and can be used as early and sensitive indicators of alteration events. Three different strategies for soil carbon sequestration were studied: minimum tillage, protection of biodegradable organic fraction by compost amendment and oxidative polimerization of soil organic matter catalyzed by biometic porfirins. All strategies were compared with a traditional agricultural management based on tillage and mineral fertilization. Experiments were carried out in three Italian soils from different pedo-climatic regions located respectively in Piacenza, Turin and Naples and cultivated with maize or wheat. Soil samples were taken for three consecutive years after harvest and analyzed for their content in phosphates, ß-glucosidase, urease and invertase. An alteration index based on these enzymatic activities levels was applied as well. The biomimetic porfirin application didn't cause changes in enzymatic activities compared to the control at any treatment or location. Enzymatic activities were generally higher in the minimum tillage and compost treatment, while differences between location and date of samplings were limited. Application of the soil alteration index based on enzymatic activities showed that soils treated with compost or subjected to minimum tillage generally have a higher biological quality. The work confirms the environmental sustainability of the carbon sequestering agronomical practices studied.

  10. Stable carbon isotope ratio variations of organic matter in Orca Basin sediments

    NASA Astrophysics Data System (ADS)

    Northam, Mark A.; Curry, David J.; Scalan, Richard S.; Parker, Patrick L.

    1981-02-01

    Orca Basin is a highly reducing basin on the slope of the Gulf of Mexico. Stable carbon isotope ratios and total organic carbon percentages were determined for two cores within the basin and one control core outside the basin. The results show that the organic carbon content of the basin cores is consistently 2-3 times greater than that of the control core. The Pleistocene-Holocene boundary, indicated by a break in the δ13C depth profile, occurs at a greater sediment depth in the basin cores than in the control core. A small sampling interval has made it possible to detect an unexplained fine structure in the δ13C profile not previously observed.

  11. Storage and release of organic carbon from glaciers and ice sheets

    USGS Publications Warehouse

    Hood, Eran; Battin, Tom J.; Fellman, Jason; O'Neel, Shad; Spencer, Robert G. M.

    2015-01-01

    Polar ice sheets and mountain glaciers, which cover roughly 11% of the Earth's land surface, store organic carbon from local and distant sources and then release it to downstream environments. Climate-driven changes to glacier runoff are expected to be larger than climate impacts on other components of the hydrological cycle, and may represent an important flux of organic carbon. A compilation of published data on dissolved organic carbon from glaciers across five continents reveals that mountain and polar glaciers represent a quantitatively important store of organic carbon. The Antarctic Ice Sheet is the repository of most of the roughly 6 petagrams (Pg) of organic carbon stored in glacier ice, but the annual release of glacier organic carbon is dominated by mountain glaciers in the case of dissolved organic carbon and the Greenland Ice Sheet in the case of particulate organic carbon. Climate change contributes to these fluxes: approximately 13% of the annual flux of glacier dissolved organic carbon is a result of glacier mass loss. These losses are expected to accelerate, leading to a cumulative loss of roughly 15 teragrams (Tg) of glacial dissolved organic carbon by 2050 due to climate change — equivalent to about half of the annual flux of dissolved organic carbon from the Amazon River. Thus, glaciers constitute a key link between terrestrial and aquatic carbon fluxes, and will be of increasing importance in land-to-ocean fluxes of organic carbon in glacierized regions.

  12. Comparison of carbon onions and carbon blacks as conductive additives for carbon supercapacitors in organic electrolytes

    NASA Astrophysics Data System (ADS)

    Jäckel, N.; Weingarth, D.; Zeiger, M.; Aslan, M.; Grobelsek, I.; Presser, V.

    2014-12-01

    This study investigates carbon onions (∼400 m2 g-1) as a conductive additive for supercapacitor electrodes of activated carbon and compares their performance with carbon black with high or low internal surface area. We provide a study of the electrical conductivity and electrochemical behavior between 2.5 and 20 mass% addition of each of these three additives to activated carbon. Structural characterization shows that the density of the resulting film electrodes depends on the degree of agglomeration and the amount of additive. Addition of low surface area carbon black (∼80 m2 g-1) enhances the power handling of carbon electrodes but significantly lowers the specific capacitance even when adding small amounts of carbon black. A much lower decrease in specific capacitance is observed for carbon onions and the best values are seen for carbon black with a high surface area (∼1390 m2 g-1). The overall performance benefits from the addition of any of the studied additives only at either high scan rates and/or electrolytes with high ion mobility. Normalization to the volume shows a severe decrease in volumetric capacitance and only at high current densities nearing 10 A g-1 we can see an improvement of the electrode capacitance.

  13. Fluvial organic carbon losses from a Bornean blackwater river

    NASA Astrophysics Data System (ADS)

    Moore, S.; Gauci, V.; Evans, C. D.; Page, S. E.

    2011-04-01

    Concentrations of dissolved organic carbon (DOC) and particulate organic carbon (POC) were analysed from the source to the mouth of the River Sebangau in Central Kalimantan, Indonesia during the dry and wet seasons in 2008/2009 and an annual total organic carbon (TOC) flux estimated. DOC concentrations were higher and POC concentrations lower in the wet season compared to the dry season. As seen in other tropical blackwater rivers, DOC concentration is consistently around 10 times greater than POC concentration. We estimate the annual TOC flux discharged to the Java Sea to be 0.46 Tg year-1 comprising of 93% (0.43 Tg) DOC and 7% (0.03 Tg) POC. This equates to a fluvial TOC loss flux per unit area over the entire Sebangau catchment of 88 g C m-2 yr-1. When extrapolating the River Sebangau DOC loss flux (83 g C m-2 yr-1) to the peat covered area of Indonesia (206 950 km2), we estimate a DOC loss of 17.2 Tg C yr-1 or ~10% of current estimates of the global annual riverine DOC discharge into the ocean.

  14. Carbon Dioxide Separation with Novel Microporous Metal Organic Frameworks

    SciTech Connect

    Richard Willis; Annabelle Benin; John Low; Ganesh Venimadhavan; Syed Faheem; David Lesch; Adam Matzger; Randy Snurr

    2008-02-04

    The goal of this program was to develop a low cost novel sorbent to remove carbon dioxide from flue gas and gasification streams in electric utilities. Porous materials named metal-organic frameworks (MOFs) were found to have good capacity and selectivity for the capture of carbon dioxide. Several materials from the initial set of reference MOFs showed extremely high CO{sub 2} adsorption capacities and very desirable linear isotherm shapes. Sample preparation occurred at a high level, with a new family of materials suitable for intellectual property protection prepared and characterized. Raman spectroscopy was shown to be useful for the facile characterization of MOF materials during adsorption and especially, desorption. Further, the development of a Raman spectroscopic-based method of determining binary adsorption isotherms was initiated. It was discovered that a stronger base functionality will need to be added to MOF linkers in order to enhance CO{sub 2} selectivity over other gases via a chemisorption mechanism. A concentrated effort was expended on being able to accurately predict CO{sub 2} selectivities and on the calculation of predicted MOF surface area values from first principles. A method of modeling hydrolysis on MOF materials that correlates with experimental data was developed and refined. Complimentary experimental data were recorded via utilization of a combinatorial chemistry heat treatment unit and high-throughput X-ray diffractometer. The three main Deliverables for the project, namely (a) a MOF for pre-combustion (e.g., IGCC) CO{sub 2} capture, (b) a MOF for post-combustion (flue gas) CO{sub 2} capture, and (c) an assessment of commercial potential for a MOF in the IGCC application, were completed. The key properties for MOFs to work in this application - high CO{sub 2} capacity, good adsorption/desorption rates, high adsorption selectivity for CO{sub 2} over other gases such as methane and nitrogen, high stability to contaminants, namely

  15. PHOTOCHEMICALLY-INDUCED ALTERATION OF STABLE CARBON ISOTOPE RATIOS (DELTA C-13) IN TERRIGENOUS DISSOLVED ORGANIC CARBON

    EPA Science Inventory

    Exposure of riverine waters to natural sunlight initiated alterations in stable carbon isotope ratios (delta C-13) of the associated dissolved organic carbon (DOC). Water samples were collected from two compositionally distinct coastal river systems in the southeastern United Sta...

  16. Direct measurement of riverine particulate organic carbon age structure

    NASA Astrophysics Data System (ADS)

    Rosenheim, Brad E.; Galy, Valier

    2012-10-01

    Carbon cycling studies focusing on transport and transformation of terrigenous carbon sources toward marine sedimentary sinks necessitate separation of particulate organic carbon (OC) derived from many different sources and integrated by river systems. Much progress has been made on isolating and characterizing young biologically-formed OC that is still chemically intact, however quantification and characterization of old, refractory rock-bound OC has remained troublesome. Quantification of both endmembers of riverine OC is important to constrain exchanges linking biologic and geologic carbon cycles and regulating atmospheric CO2 and O2. Here, we constrain petrogenic OC proportions in suspended sediment from the headwaters of the Ganges River in Nepal through direct measurement using ramped pyrolysis radiocarbon analysis. The unique results apportion the biospheric and petrogenic fractions of bulk particulate OC and characterize biospheric OC residence time. Compared to the same treatment of POC from the lower Mississippi-Atchafalaya River system, contrast in age spectra of the Ganges tributary samples illustrates the difference between small mountainous river systems and large integrative ones in terms of the global carbon cycle.

  17. Particulate organic matter composition and organic carbon flux in Arctic valley glaciers: examples from the Bayelva River and adjacent Kongsfjorden

    NASA Astrophysics Data System (ADS)

    Zhu, Z.-Y.; Wu, Y.; Liu, S.-M.; Wenger, F.; Hu, J.; Zhang, J.; Zhang, R.-F.

    2015-09-01

    In the face of ongoing global warming and glacier retreat, the composition and flux of organic matter in glacier-fjord systems are key variables for updating the carbon cycle and budget, whereas the role of Arctic valley glaciers seems unimportant when compared with the huge Greenland Ice Sheet. Our field observations of the glacier-fed Bayelva River, Svalbard, and the adjacent Kongsfjorden allowed us to determine the compositions of particulate organic matter from glacier to fjord and also to estimate the flux of organic carbon, both for the river and for Svalbard in general. Particulate organic carbon (POC) and dissolved organic carbon (DOC) in the Bayelva River averaged 56 and 73 μM, respectively, in August 2012. Amino acids (AAs) and phytoplankton pigments accounted for ~ 10 % of the particulate organic matter (POM) in the Bayelva River, while AAs represented > 90 % of particulate nitrogen in fjord surface water, suggesting the strong in situ assimilation of organic matter. Bacteria accounts for 13 and 19 % of the POC in the Bayelva River and the Kongsfjorden, respectively, while values for particulate nitrogen (PN) are much higher (i.e., 36 % in Kongsfjorden). The total discharge from the Bayelva River in 2012 was 29 × 106 m3. Furthermore, we calculated the annual POC, DOC, and PN fluxes for the river as 20 ± 1.6, 25 ± 5.6, and 4.7 ± 0.75 t, respectively. Using the POC content and DOC concentration data, we then estimated the annual POC and DOC fluxes for Svalbard glaciers. Although the estimated POC (0.056 ± 0.02 × 106 t yr-1) and DOC (0.02 ± 0.01 × 106 t yr-1) fluxes of Svalbard glaciers are small compared with those of the Greenland Ice Sheet, the area-weighted POC flux of Svalbard glaciers is twice that of the Greenland Ice Sheet, while the flux of DOC can be 4 to 7 times higher. Therefore, we propose that valley glaciers are efficient high-latitude sources of organic carbon.

  18. Carbon storage in Organic Soils (COrS): Quantifying past variations in carbon accumulation in peatlands of South Wales, UK.

    NASA Astrophysics Data System (ADS)

    Carless, Donna; Kulessa, Bernd; Street-Perrott, Alayne; Davies, Siwan; Sinnadurai, Paul

    2014-05-01

    Globally, peatlands comprise a vital terrestrial carbon sink, currently estimated to be around 500 PgC (Yu et al., 2011, Gorham, 1991). Within the UK, peatlands represent the single most important terrestrial carbon store (IUCN, 2011). In particular, blanket and raised bogs account for around 23,000 square kilometres or 9.5 percent of the UK land area, with current estimates indicating that they store approximately 3.2 PgC (IUCN, 2011). Recent studies suggest that carbon-sequestration rates have been highly variable during the Holocene (Frolking & Roulet, 2007). Reconstructing these past fluctuations is essential to assess how peatlands will respond to future climate change, particularly the possibility that large amounts of respired below-ground carbon will be released as a result of enhanced rates of decomposition, causing positive climate feedback. Quantitative estimates of past variations in carbon accumulation provide valuable insights into the factors controlling carbon budgets. Recent developments have illustrated how ground-penetrating radar (GPR) can improve constraints on peat thickness (Holden et al., 2002, Warner et al., 1990), facilitating site-specific peat-volume estimates for carbon quantification. We shall present initial results from the COrS project, which brings together a novel combination of geophysical and proxy techniques to reconstruct variations in long-term carbon accumulation in 6 ombrotrophic peat bogs, located across the Brecon Beacons National Park (BBNP), South Wales, UK (51°55'30" N, 3°29'18" W). Detailed GPR surveys are being used to provide comprehensive estimates of total peat extent and thickness at these sites. Combined with surface-elevation data from LiDAR imagery, 3D models are being created, from which total peat-volume estimates will be extracted. Carbon-accumulation rates will be inferred from these bog-volume estimates, coupled with total organic carbon (TOC) measurements and high-resolution radiocarbon dating. In

  19. Mesoporous carbon-zirconium oxide nanocomposite derived from carbonized metal organic framework: A coating for solid-phase microextraction.

    PubMed

    Saraji, Mohammad; Mehrafza, Narges

    2016-08-19

    In this paper, a mesoporous carbon-ZrO2 nanocomposite was fabricated on a stainless steel wire for the first time and used as the solid-phase microextraction coating. The fiber was synthesized with the direct carbonization of a Zr-based metal organic framework. With the utilization of the metal organic framework as the precursor, no additional carbon source was used for the synthesis of the mesoporous carbon-ZrO2 nanocomposite coating. The fiber was applied for the determination of BTEX compounds (benzene, toluene, ethylbenzene and m, p-xylenes) in different water samples prior to gas chromatography-flame ionization detection. Such important experimental factors as synthesis time and temperature, salt concentration, equilibrium and extraction time, extraction temperature, desorption time and desorption temperature were studied and optimized. Good linearity in the concentration range of 0.2-200μgL(-1) and detection limits in the range of 0.05-0.56μgL(-1) was achieved for BTEX compounds. The intra- and inter-day relative standard deviations were in the range of 3.5-4.8% and 4.9-6.7%, respectively. The prepared fiber showed high capability for the analysis of BTEX compounds in different water and wastewater samples with good relative recoveries in the range of 93-107%. PMID:27451259

  20. Dissolved Organic Carbon Cycling in Forested Watersheds: A Carbon Isotope Approach

    NASA Astrophysics Data System (ADS)

    Schiff, S. L.; Aravena, R.; Trumbore, S. E.; Dillon, P. J.

    1990-12-01

    Dissolved organic carbon (DOC) is important in the acid-base chemistry of acid-sensitive freshwater systems; in the complexation, mobility, persistence, and toxicity of metals and other pollutants; and in lake carbon metabolism. Carbon isotopes (13C and 14C) are used to study the origin, transport, and fate of DOC in a softwater catchment in central Ontario. Precipitation, soil percolates, groundwaters, stream, beaver pond, and lake waters, and lake sediment pore water were characterized chemically and isotopically. In addition to total DOC, isotopic measurements were made on the humic and fulvic DOC fractions. The lake is a net sink for DOC. Δ14C results indicate that the turnover time of most of the DOC in streams, lakes, and wetlands is fast, less than 40 years, and on the same time scale as changes in acidic deposition. DOC in groundwaters is composed of older carbon than surface waters, indicating extensive cycling of DOC in the upper soil zone or aquifer.

  1. Stable Carbon Isotopic Signatures of Abiotic Organics from Hydrothermal Synthesis Experiments

    NASA Technical Reports Server (NTRS)

    Stern, Jennifer C.; Summers, David P.; Kubo, Mike; Yassar, Saima

    2006-01-01

    Stable carbon isotopes can be powerful biogeochemical markers in the study of life's origins. Biogenic carbon fixation produces organics that are depleted in C-13 by about -20 to -30%0. Less attention has been paid to the isotopic signatures of abiotic processes. The possibility of abiotic processes producing organics with morphologies and isotopic signatures in the biogenic range has been at the center of recent debate over the Earth's earliest microfossils. The abiotic synthesis of organic compounds in hydrothermal environments is one possible source of endogenous organic matter to the prebiotic earth. Simulated hydrothermal settings have been shown to synthesize, among other things, single chain amphiphiles and simple lipids from a mix of CO, CO2, and H2. A key characteristic of these amphiphilic molecules is the ability to self-assemble in aqueous phases into more organized structures called vesicles, which form a selectively permeable boundary and serve the function of containing and concentrating other organic molecules. The ability to form cell like structures also makes these compounds more likely to be mistaken for biogenic. Hydrothermal simulation experiments were conducted from oxalic or formic acid in water at 175 C for 72 hr. The molecular and isotopic composition of the products of these reactions were determined and compared to biogenic fractionations . Preliminary results indicate isotopic fractionation during abiotic hydrocarbon synthesis in hydrothermal environments is on par with biological carbon fixation.

  2. Impacts of crop rotations on soil organic carbon sequestration

    NASA Astrophysics Data System (ADS)

    Gobin, Anne; Vos, Johan; Joris, Ingeborg; Van De Vreken, Philippe

    2013-04-01

    Agricultural land use and crop rotations can greatly affect the amount of carbon sequestered in the soil. We developed a framework for modelling the impacts of crop rotations on soil carbon sequestration at the field scale with test case Flanders. A crop rotation geo-database was constructed covering 10 years of crop rotation in Flanders using the IACS parcel registration (Integrated Administration and Control System) to elicit the most common crop rotation on major soil types in Flanders. In order to simulate the impact of crop cover on carbon sequestration, the Roth-C model was adapted to Flanders' environment and coupled to common crop rotations extracted from the IACS geodatabases and statistical databases on crop yield. Crop allometric models were used to calculate crop residues from common crops in Flanders and subsequently derive stable organic matter fluxes to the soil (REGSOM). The REGSOM model was coupled to Roth-C model was run for 30 years and for all combinations of seven main arable crops, two common catch crops and two common dosages of organic manure. The common crops are winter wheat, winter barley, sugar beet, potato, grain maize, silage maize and winter rapeseed; the catch crops are yellow mustard and Italian ryegrass; the manure dosages are 35 ton/ha cattle slurry and 22 ton/ha pig slurry. Four common soils were simulated: sand, loam, sandy loam and clay. In total more than 2.4 million simulations were made with monthly output of carbon content for 30 years. Results demonstrate that crop cover dynamics influence carbon sequestration for a very large percentage. For the same rotations carbon sequestration is highest on clay soils and lowest on sandy soils. Crop residues of grain maize and winter wheat followed by catch crops contribute largely to the total carbon sequestered. This implies that agricultural policies that impact on agricultural land management influence soil carbon sequestration for a large percentage. The framework is therefore

  3. Carbon uptake in low dissolved inorganic carbon environments: the effect of limited carbon availability on photosynthetic organisms in thermal waters

    NASA Astrophysics Data System (ADS)

    Myers, K. D.; Omelon, C. R.; Bennett, P.

    2010-12-01

    Photosynthesis is the primary carbon fixation process in thermal waters below 70°C, but some hydrothermal waters have extremely low dissolved inorganic carbon (DIC), potentially limiting the growth of inorganic carbon fixing organisms such as algae and cyanobacteria. To address the issue of how carbon is assimilated by phototrophs in these environments, we conducted experiments to compare inorganic carbon uptake mechanisms by two phylogenetically distinct organisms collected from geographically distinct carbon limited systems: the neutral pH geothermal waters of El Tatio, Chile, and the acidic geothermal waters of Tantalus Creek in Norris Geyser Basin, Yellowstone National Park. Discharge waters at El Tatio have low total DIC concentrations (2 to 6 ppm) found mainly as HCO3-; this is in contrast to even lower measured DIC values in Tantalus Creek (as low as 0.13 ppm) that, due to a measured pH of 2.5, exists primarily as CO2. Cyanobacteria and algae are innately physiologically plastic, and we are looking to explore the possibility that carbon limitation in these environments is extreme enough to challenge that plasticity and lead to a suite of carbon uptake adaptations. We hypothesize that these microorganisms utilize adaptive modes of Ci uptake that allow them to survive under these limiting conditions. Cyanobacteria (primarily Synechococcus spp.) isolated from El Tatio can utilize either passive CO2 uptake or active HCO3- uptake mechanisms, in contrast to the eukaryotic alga Cyanidium spp. from Tantalus Creek, which is restricted to an energy-dependent CO2 uptake mechanism. To test this hypothesis, we conducted pH drift experiments (Omelon et al., 2008) to examine changes in pH and [DIC] under a range of pH and [DIC] culture conditions. This work provides baseline information upon which we will begin to investigate the effects of low [DIC] on the growth of phototrophs collected from these and other less carbon limited systems.

  4. Determination of total dissolved inorganic carbon in freshwaters by reagent-free ion chromatography.

    PubMed

    Polesello, Stefano; Tartari, Gabriele; Giacomotti, Paola; Mosello, Rosario; Cavalli, Silvano

    2006-06-16

    Studies of inorganic carbon cycle in natural waters provide important information on the biological productivity and buffer capacity. Determination of total inorganic carbon, alkalinity and dissolved carbon dioxide gives an indication of the balance between photosynthesis and respiration by biota, both within the water column and sediments, and carbon dioxide transfers from the water column to the atmosphere. There are few methods to measure and distinguish the different forms of inorganic carbon, but all require a measure or an indirect quantification of total inorganic carbon. A direct measurement of TIC in water is made possible by the introduction of electrolytic generated hydroxide eluent in ion chromatography which allows to detect a chromatographic peak for carbonate. The advantage of this method is that all the inorganic forms of carbon are converted in carbonate at eluent pH and can be detected as a single peak by conductivity detection. Repeatability of carbonate peak was evaluated at different levels from 0.02 to 6 mequiv.l(-1) both in high purity water and in real samples and ranged from 1 to 9%. The calibration curve was not linear and has to be fitted by a quadratic curve. Limit of detection was estimated to be 0.02 mequiv.l(-1). Accuracy has been estimated by comparing ion chromatography method with total inorganic carbon calculated from alkalinity and pH. The correlation between the two methods was good (R(2)=0.978, n=141). The IC method has been applied to different typologies of surface waters (alpine and subalpine lakes and rivers) characterised by different chemical characteristics (alkalinity from 0.05 to 2 mequiv.l(-1) and pH from 6.7 to 8.5) and low total organic carbon concentrations. This analytical method allowed to describe the distribution of TIC along the water column of two Italian deep lakes. PMID:16620857

  5. CHEMISTRY OF DISSOLVED ORGANIC CARBON AND ORGANIC ACIDS IN TWO STREAMS DRAINING FORESTED WATERSHEDS

    EPA Science Inventory

    The concentration, major fractions, and contribution of dissolved organic carbon (DOG) to stream chemistry were examined in two paired streams draining upland catchments in eastern Maine. oncentrations of DOC in East and West Bear Brooks were 183 +/- 73 and 169 +/- 70 umol CL-1 (...

  6. Three powerful dinuclear metal-organic catalysts for converting CO2 into organic carbonates.

    PubMed

    Zhao, Dan; Liu, Xiao-Hui; Shi, Zhuang-Zhi; Zhu, Chen-Dan; Zhao, Yue; Wang, Peng; Sun, Wei-Yin

    2016-09-28

    Developing efficient catalysts for converting carbon dioxide (CO2) into varied organic carbonates is an important scientific goal. By using the NH2-functionalized tripodal ligand 2-((bis(2-aminoethyl)amino)methyl)phenol (HL), three dinuclear metal-organic complexes [Zn(L)]2·2ClO4 (1), [Cu(L)]2·2ClO4·2H2O (2) and [Cd(L)]2·2ClO4 (3) have been successfully isolated and structurally characterized using single-crystal X-ray diffraction analyses. Considering the dinuclear metal centers and the NH2-functional groups in the structures, 1-3 were investigated as catalysts for converting CO2 into organic carbonates, and the results show that 1-3 exhibit an outstanding ability for converting CO2 into varied organic carbonates at atmospheric pressure (0.1 MPa). The catalytic system also displays a wide substrate scope and high catalytic activity, and the reaction mechanism has been proposed herein. PMID:27530724

  7. Fate of Soil Organic Carbon and Polycyclic Aromatic Hydrocarbons in a Vineyard Soil Treated with Biochar.

    PubMed

    Rombolà, Alessandro G; Meredith, Will; Snape, Colin E; Baronti, Silvia; Genesio, Lorenzo; Vaccari, Francesco Primo; Miglietta, Franco; Fabbri, Daniele

    2015-09-15

    The effect of biochar addition on the levels of black carbon (BC) and polcyclic aromatic hydrocarbons (PAHs) in a vineyard soil in central Italy was investigated within a two year period. Hydropyrolysis (HyPy) was used to determine the contents of BC (BCHyPy) in the amended and control soils, while the hydrocarbon composition of the semi-labile (non-BCHyPy) fraction released by HyPy was determined by gas chromatography-mass spectrometry, together with the solvent-extractable PAHs. The concentrations of these three polycyclic aromatic carbon reservoirs changed and impacted differently the soil organic carbon over the period of the trial. The addition of biochar (33 ton dry biochar ha(-1)) gave rise to a sharp increase in soil organic carbon, which could be accounted for by an increase in BCHyPy. Over time, the concentration of BCHyPy decreased significantly from 36 to 23 mg g(-1) and as a carbon percentage from 79% to 61%. No clear time trends were observed for the non-BCHyPy PAHs varying from 39 to 34 μg g(-1) in treated soils, not significantly different from control soils. However, the concentrations of extractable PAHs increased markedly in the amended soils and decreased with time from 153 to 78 ng g(-1) remaining always higher than those in untreated soil. The extent of the BCHyPy loss was more compatible with physical rather than chemical processes. PMID:26263378

  8. The sorption of organic matter in soils as affected by the nature of soil carbon

    SciTech Connect

    Kaiser, K.; Haumaier, L.; Zech, W.

    2000-04-01

    Recent studies have shown that soil organic carbon (OC) may either hinder or favor the sorption of dissolved organic matter (DOM) in soils. The concept was that the nature of soil OC determines these contrasting findings. To test this hypothesis, the authors compared the DOM sorption in soils with OC derived from biomass decomposition with that in soils with OC more likely derived from biomass decomposition with that in soils with OC more likely derived from charred materials (black carbon). All the mineral soil samples in the study were from Spodosols, and the DOM was from an aqueous extract of a more forest floor layer. Sorption was determined in batch experiments. The sorption in soils that contain large amounts of black carbon was, in general, less than the sorption in soils with decomposition-derived OC. When the DOM sorption parameters of the soils were correlated to the OC content, the black carbon soils showed a positive effect of the OC content on the DOM sorption. In the soils lacking the features of black carbon residues, the DOM sorption was negatively influenced by OC. These results lead them to assume that the nature of soil OC is a soil property that needs to be considered in the DOM sorption of soils, especially when soils have large amounts of highly aromatic OC.

  9. Determinism, chaos, self-organization and entropy.

    PubMed

    Pontes, José

    2016-01-01

    We discuss two changes of paradigms that occurred in science along the XXth century: the end of the mechanist determinism, and the end of the apparent incompatibility between biology, where emergence of order is law, and physics, postulating a progressive loss of order in natural systems. We recognize today that three mechanisms play a major role in the building of order: the nonlinear nature of most evolution laws, along with distance to equilibrium, and with the new paradigm, that emerged in the last forty years, as we recognize that networks present collective order properties not found in the individual nodes. We also address the result presented by Blumenfeld (L.A. Blumenfeld, Problems of Biological Physics, Springer, Berlin, 1981) showing that entropy decreases resulting from building one of the most complex biological structures, the human being, are small and may be trivially compensated for compliance with thermodynamics. Life is made at the expense of very low thermodynamic cost, so thermodynamics does not pose major restrictions to the emergence of life. Besides, entropy does not capture our idea of order in biological systems. The above questions show that science is not free of confl icts and backlashes, often resulting from excessive extrapolations. PMID:27331802

  10. Dissolved organic carbon (DOC) in Arctic ground ice

    NASA Astrophysics Data System (ADS)

    Fritz, M.; Opel, T.; Tanski, G.; Herzschuh, U.; Meyer, H.; Eulenburg, A.; Lantuit, H.

    2015-01-01

    Thermal permafrost degradation and coastal erosion in the Arctic remobilize substantial amounts of organic carbon (OC) and nutrients which have been accumulated in late Pleistocene and Holocene unconsolidated deposits. Their vulnerability to thaw subsidence, collapsing coastlines and irreversible landscape change is largely due to the presence of large amounts of massive ground ice such as ice wedges. However, ground ice has not, until now, been considered to be a source of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC) and other elements, which are important for ecosystems and carbon cycling. Here we show, using geochemical data from a large number of different ice bodies throughout the Arctic, that ice wedges have the greatest potential for DOC storage with a maximum of 28.6 mg L-1 (mean: 9.6 mg L-1). Variation in DOC concentration is positively correlated with and explained by the concentrations and relative amounts of typically terrestrial cations such as Mg2+ and K+. DOC sequestration into ground ice was more effective during the late Pleistocene than during the Holocene, which can be explained by rapid sediment and OC accumulation, the prevalence of more easily degradable vegetation and immediate incorporation into permafrost. We assume that pristine snowmelt is able to leach considerable amounts of well-preserved and highly bioavailable DOC as well as other elements from surface sediments, which are rapidly stored in ground ice, especially in ice wedges, even before further degradation. In the Yedoma region ice wedges represent a significant DOC (45.2 Tg) and DIC (33.6 Tg) pool in permafrost areas and a fresh-water reservoir of 4172 km3. This study underlines the need to discriminate between particulate OC and DOC to assess the availability and vulnerability of the permafrost carbon pool for ecosystems and climate feedback upon mobilization.

  11. Dissolved organic carbon (DOC) in Arctic ground ice

    NASA Astrophysics Data System (ADS)

    Fritz, M.; Opel, T.; Tanski, G.; Herzschuh, U.; Meyer, H.; Eulenburg, A.; Lantuit, H.

    2015-04-01

    Thermal permafrost degradation and coastal erosion in the Arctic remobilize substantial amounts of organic carbon (OC) and nutrients which have accumulated in late Pleistocene and Holocene unconsolidated deposits. Permafrost vulnerability to thaw subsidence, collapsing coastlines and irreversible landscape change are largely due to the presence of large amounts of massive ground ice such as ice wedges. However, ground ice has not, until now, been considered to be a source of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC) and other elements which are important for ecosystems and carbon cycling. Here we show, using biogeochemical data from a large number of different ice bodies throughout the Arctic, that ice wedges have the greatest potential for DOC storage, with a maximum of 28.6 mg L-1 (mean: 9.6 mg L-1). Variation in DOC concentration is positively correlated with and explained by the concentrations and relative amounts of typically terrestrial cations such as Mg2+ and K+. DOC sequestration into ground ice was more effective during the late Pleistocene than during the Holocene, which can be explained by rapid sediment and OC accumulation, the prevalence of more easily degradable vegetation and immediate incorporation into permafrost. We assume that pristine snowmelt is able to leach considerable amounts of well-preserved and highly bioavailable DOC as well as other elements from surface sediments, which are rapidly frozen and stored in ground ice, especially in ice wedges, even before further degradation. We found that ice wedges in the Yedoma region represent a significant DOC (45.2 Tg) and DIC (33.6 Tg) pool in permafrost areas and a freshwater reservoir of 4200 km2. This study underlines the need to discriminate between particulate OC and DOC to assess the availability and vulnerability of the permafrost carbon pool for ecosystems and climate feedback upon mobilization.

  12. Organic carbon redistribution due to erosion at various spatial scales

    NASA Astrophysics Data System (ADS)

    Jakab, Gergely; Szabó, Judit; Szalai, Zoltán; Mészáros, Erzsébet; Szabó, Boglárka; Centeri, Csaba

    2016-04-01

    Soil organic carbon (SOC) has a crucial role both in terms of crop production and climate change mitigation. Soil could be an effective sink of atmospheric carbon since in agricultural areas the carbon content of the soil is much lower than its capacity. The main obstacle against carbon charge of the soils is cultivation and erosion. Soil detachment, delivery and deposition are rather scale dependent processes that is why it is difficult to compare or extrapolate results among scales. Present case study aims to compare the SOC content and soil organic matter (SOM) compound of the detached soil particles on the ridge to those that are deposited at the bottom of the catena in order to clarify the role of delivery in soil erosion. Initial soil erosion was modelled using a laboratory rainfall simulator at the point scale. Deposition was surveyed and analysed by 3D sampling from drillings on the sedimentary parts at the field scale. At the detachment phase carbon enrichment (50-100%) and C/N ratio increase were found in each aggregate size class of the detached soil particles. Variations in SOM compounds suggested that a very intensive SOM exchange took place during initial erosion processes and delivery. In addition to the selective erosion selective SOC deposition were also found at the field scale. Two topographical hotspots were identified as the place of SOC surplus deposition. In these patches SOM compounds were deposited separately due to different geomorphologic positions. The lower patch next to the end of an ephemeral gully was dominated by less polymerized more aromatic SOM, while the upper one was ruled by high molecular weighted aliphatic SOM. Difference in SOM compound was manifested also in different sediment morphology. The topographically higher deposition patch were covered by aggregates while the lower one was found to be sealed by individual soil particles. Present study was supported by the National Hungarian Research Found K100180, G. Jakab was

  13. Adsorption equilibrium of organic vapors on single-walled carbon nanotubes

    USGS Publications Warehouse

    Agnihotri, S.; Rood, M.J.; Rostam-Abadi, M.

    2005-01-01

    Gravimetric techniques were employed to determine the adsorption capacities of commercially available purified electric arc and HiPco single-walled carbon nanotubes (SWNTs) for organic compounds (toluene, methyl ethyl ketone (MEK), hexane and cyclohexane) at relative pressures, p/p0, ranging from 1 ?? 10-4 to 0.95 and at isothermal conditions of 25, 37 and 50 ??C. The isotherms displayed both type I and type II characteristics. Adsorption isotherm modeling showed that SWNTs are heterogeneous adsorbents, and the Freundlich equation best describes the interaction between organic molecules and SWNTs. The heats of adsorption were 1-4 times the heats of vaporization, which is typical for physical adsorption of organic vapors on porous carbons. ?? 2005 Elsevier Ltd. All rights reserved.

  14. Estimating organic micro-pollutant removal potential of activated carbons using UV absorption and carbon characteristics.

    PubMed

    Zietzschmann, Frederik; Altmann, Johannes; Ruhl, Aki Sebastian; Dünnbier, Uwe; Dommisch, Ingvild; Sperlich, Alexander; Meinel, Felix; Jekel, Martin

    2014-06-01

    Eight commercially available powdered activated carbons (PAC) were examined regarding organic micro-pollutant (OMP) removal efficiencies in wastewater treatment plant (WWTP) effluent. PAC characteristic numbers such as B.E.T. surface, iodine number and nitrobenzene number were checked for their potential to predict the OMP removal of the PAC products. Furthermore, the PAC-induced removal of UV254 nm absorption (UVA254) in WWTP effluent was determined and also correlated with OMP removal. None of the PAC characteristic numbers can satisfactorily describe OMP removal and accordingly, these characteristics have little informative value on the reduction of OMP concentrations in WWTP effluent. In contrast, UVA254 removal and OMP removal correlate well for carbamazepine, diclofenac, and several iodinated x-ray contrast media. Also, UVA254 removal can roughly describe the average OMP removal of all measured OMP, and can accordingly predict PAC performance in OMP removal. We therefore suggest UVA254 as a handy indicator for the approximation of OMP removal in practical applications where direct OMP concentration quantification is not always available. In continuous operation of large-scale plants, this approach allows for the efficient adjustment of PAC dosing to UVA254, in order to ensure reliable OMP removal whilst minimizing PAC consumption. PMID:24651017

  15. Soil organic carbon, macropore networks and preferential transport

    NASA Astrophysics Data System (ADS)

    Larsbo, Mats; Koestel, John; Kätterer, Thomas; Jarvis, Nick

    2016-04-01

    Agricultural management practices such as tillage, crop rotations, residue management and fertilization can have a strong influence on soil organic carbon (SOC) stocks. An increase in SOC content will generally improve soil structure, which in turn determines the solute transport pathways through the soil. The aim of this study was to quantify the architecture of macropore networks in undisturbed soil columns (15 cm high, 12.7 cm diameter) sampled along a transect with natural variations in SOC using X-ray tomography and to relate the network characteristics to the degree of preferential transport in the columns. Two tracer experiments were carried out at constant irrigation rates of 2 and 5 mm h-1. We used the normalised 5% arrival time which reflects the tendency for early arrival of the solutes as a measure of the degree of preferential transport. The soil macropore networks were analysed in cylindrical sub-volumes (8 cm high, 10 cm diameter) located centrally within the soil columns. These sub-volumes were considered unaffected by sampling artefacts. Analyses were also carried out the for whole sample volumes to enable comparisons with the results from the transport experiments. Image processing and analysis were carried out in ImageJ and R. The same grey value threshold was applied to all images after harmonisation of grey values using the PVC column walls and the air outside the columns. This approach resulted in a satisfactory separation between the pore space and the surrounding soil matrix and organic matter. The SOC content along the transect, which varied from 4.2 to 15% , was correlated to all measures of the pore network for the sub-volumes except for the connectivity probability. Columns with high SOC content were associated with large macroporosities (both total and connected), large specific surface areas, large fractal dimensions and small mean pore thicknesses. The SOC content for whole sample volumes was positively correlated to 5% arrival times

  16. Colloidal stability and ecotoxicity of multiwalled carbon nanotubes: Influence of select organic matters.

    PubMed

    Cerrillo, Cristina; Barandika, Gotzone; Igartua, Amaya; Areitioaurtena, Olatz; Uranga, Nerea; Mendoza, Gemma

    2016-01-01

    In the last few years, the release of multiwalled carbon nanotubes (MWCNTs) into the environment has raised serious concerns regarding their fate and potential impacts. Aquatic organisms constitute an important pathway for their entrance and transfer throughout the food web, and the current demand for standardization of methodologies to analyze the interactions of MWCNTs with them requires aquatic media that represent natural systems. However, the inherent hydrophobicity of MWCNTs and the substances present in natural waters may greatly affect their stability and bioavailability. The present study analyzes the influence of the most referenced synthetic and natural organic matters (Sigma-Aldrich humic acid and Suwannee River natural organic matter) in the agglomeration kinetics and ecotoxicity of MWCNTs, with the aim of determining their suitability to fulfill the current standardization requirements. Natural organic matter provides increased colloidal stability to the MWCNTs' dispersions, which results in higher adverse effects on the key invertebrate organism Daphnia magna. Furthermore, the results obtained with this type of organic matter allow for observation of the important role of the outer diameter and content impurities of MWCNTs in their stability and ecotoxicity on daphnids. Sigma-Aldrich humic acid appeared to alter the response of the organisms to carbon nanotubes compared with that observed in the presence of natural organic matter. PMID:26189503

  17. Organic carbon burial in a mangrove forest, margin and intertidal mud flat

    NASA Astrophysics Data System (ADS)

    Sanders, Christian J.; Smoak, Joseph M.; Naidu, A. Sathy; Sanders, Luciana M.; Patchineelam, Sambasiva R.

    2010-12-01

    The flux of total organic carbon (TOC) to depositional facies (intertidal mud flat, margin and forest) was quantified for a tropical mangrove forest in Brazil. Results indicate that these mangrove margins and intertidal mudflats are sites of large TOC accumulation, almost four times greater than the global averages for mangrove forests. The TOC burial rates were determined from organic carbon content in sediment cores which were dated using 210Pb. Burial rates were calculated to be 1129, 949, and 353 (g m -2 yr -1), for the mud flat, margin and forest, respectively. Sediment accumulation rates (SAR) were estimated to be 7.3, 5.0 and 2.8 mm yr -1. Sediment characterization (δ 13C, δ 15N, TOC/TN and mud fraction) indicated a representative mangrove system with a record of consistent organic matter flux of up to 100 years. Because of substantial burial of organic carbon in mangrove ecosystems, their role in the global carbon budget must be considered. More importantly, as climate change influences temperature and sea level, mangrove ecosystems will respond to specific climatic conditions.

  18. Metal doped carbon nanoneedles and effect of carbon organization with activity for hydrogen evolution reaction (HER).

    PubMed

    Araujo, Rafael A; Rubira, Adley F; Asefa, Tewodros; Silva, Rafael

    2016-02-10

    Cellulose nanowhiskers (CNW) from cotton, was prepared by acid hydrolysis and purified using a size selection process to obtain homogeneous samples with average particle size of 270 nm and 85.5% crystallinity. Purified CNW was used as precursor to carbon nanoneedles (CNN) synthesis. The synthesis of CNN loaded with different metals dopants were carried out by a nanoreactor method and the obtained CNNs applied as electrocatalysts for hydrogen evolution reaction (HER). In the carbon nanoneedles synthesis, Ni, Cu, or Fe worked as graphitization catalyst and the metal were found present as dopants in the final material. The used metal appeared to have direct influence on the degree of organization of the particles and also in the surface density of polar groups. It was evaluated the influence of the graphitic organization on the general properties and nickel was found as the more appropriate metal since it leads to a more organized material and also to a high activity toward HER. PMID:26686184

  19. Effects of iron-aluminium oxides and organic carbon on aggregate stability of bauxite residues.

    PubMed

    Zhu, Feng; Li, Yubing; Xue, Shengguo; Hartley, William; Wu, Hao

    2016-05-01

    In order to successfully establish vegetation on bauxite residue, properties such as aggregate structure and stability require improvement. Spontaneous plant colonization on the deposits in Central China over the last 20 years has revealed that natural processes may improve the physical condition of bauxite residues. Samples from three different stacking ages were selected to determine aggregate formation and stability and its relationship with iron-aluminium oxides and organic carbon. The residue aggregate particles became coarser in both dry and wet sieving processes. The mean weight diameter (MWD) and geometry mean diameter (GMD) increased significantly, and the proportion of aggregate destruction (PAD) decreased. Natural stacking processes could increase aggregate stability and erosion resistant of bauxite residues. Free iron oxides and amorphous aluminium oxides were the major forms in bauxite residues, but there was no significant correlation between the iron-aluminium oxides and aggregate stability. Aromatic-C, alkanes-C, aliphatic-C and alkenes-C were the major functional groups present in the residues. With increasing stacking age, total organic carbon content and aggregate-associated organic carbon both increased. Alkanes-C, aliphatic-C and alkenes-C increased and were mainly distributed in macro-aggregates, whereas aromatic-C was mainly distributed in <0.05-mm aggregates. Organic carbon stability in micro-aggregates was higher than that in macro-aggregates and became more stable. Organic carbon contents in total residues, and within different aggregate sizes, were all negatively correlated with PAD. It indicated that organic materials had a more significant effect on macro-aggregate stability and the effects of iron-aluminium oxides maybe more important for stability of micro-aggregates. PMID:26832865

  20. DETERMINING INTERSTELLAR CARBON ABUNDANCES FROM STRONG-LINE TRANSITIONS

    SciTech Connect

    Sofia, U. J.; Parvathi, V. S.; Babu, B. R. S.; Murthy, J.

    2011-01-15

    Carbon is arguably the most important element in the interstellar medium, yet its abundance in gas and dust is poorly understood due to a paucity of data. We explore the possibility of substantially increasing our knowledge of interstellar carbon by applying and assessing a new method for determining the column density of the dominant ion of interstellar carbon in diffuse neutral lines of sight. The method relies on profile fitting of the strong transition of C II at 1334 A in spectra continuum normalized with stellar models. We apply our method to six sight lines for which the carbon abundance has previously been determined with a weak intersystem absorption transition. Our strong-line method consistently shows a significantly lower gas-phase C abundance than the measurements from the weak lines. This result implies that more carbon could reside in dust than was previously thought. This has implications for dust models, which often suffer from a lack of sufficient carbon to plausibly explain extinction. There is no immediately clear explanation for the difference found between the strong- and weak-line C II determinations, but there are indications that the results from the method presented here have advantages over the weak-line column densities. If this is the case, then the reported oscillator strength for the C II transition at 2325 A may be too small. Our findings further suggest that damping wings modeled with a single absorption component may not produce accurate abundances. This problem could affect a large number of H I abundances determined through absorption line analysis that are reported in the literature.

  1. Organic carbon in glacial fjords of Chilean Patagonia

    NASA Astrophysics Data System (ADS)

    Pantoja, Silvio; Gutiérrez, Marcelo; Tapia, Fabián; Abarzúa, Leslie; Daneri, Giovanni; Reid, Brian; Díez, Beatriz

    2016-04-01

    The Southern Ice Field in Chilean Patagonia is the largest (13,000 km2) temperate ice mass in the Southern hemisphere, yearly transporting ca. 40 km3 of freshwater to fjords. This volume of fresh and cold water likely affects adjacent marine ecosystems by changing circulation, productivity, food web dynamics, and the abundance and distribution of planktonic and benthic organisms. We hypothesize that freshwater-driven availability of inorganic nutrient and transport of organic and inorganic suspended matter, as well as microbes, become a controlling factor for productivity in the fjord associated with the Baker river and Jorge Montt glacier. Both appear to be sources of silicic acid, but not of nitrate and particulate organic carbon, especially during summer, when surface PAR and glacier thawing are maximal. In contrast to Baker River, the Jorge Montt glacier is also a source of dissolved organic carbon towards a proglacial fjord and the Baker Channel, indicating that a thorough chemical description of sources (tidewater glacier and glacial river) is needed. Nitrate in fiord waters reaches ca. 15 μM at 25 m depth with no evidence of mixing up during summer. Stable isotope composition of particulate organic nitrogen reaches values as low as 3 per mil in low-salinity waters near both glacier and river. Nitrogen fixation could be depleting δ15N in organic matter, as suggested by the detection at surface waters of nif H genes belonging to diazotrophs near the Montt glacier. As diazotrophs have also been detected in other cold marine waters (e.g. Baltic Sea, Arctic Ocean) as well as glaciers and polar terrestrial waters, there is certainly a potential for both marine and freshwater microbes to contribute and have a significant impact on the Patagonian N and C budgets. Assessing the impact of freshwater on C and N fluxes and the microbial community structure in Patagonian waters will allow understanding future scenarios of rapid glacier melting. This research was funded

  2. [Determination of carbon-centred radicals in mainstream cigarette smoke using spin-labelled fluorophore].

    PubMed

    Bian, Zhaoyang; Tang, Gangling; Yang, Fei; Pang, Yongqiang; Zhang, Hongfei; Hu, Qingyuan

    2012-06-01

    A method of the determination of the carbon-centred radicals in mainstream cigarette smoke using a spin-labelled fluorophore, 4-((9-acridinecarbonyl) amino)-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO-9-AC), as a fluorescent probe is presented. After being producted by smoking in International Organization for Standardization (ISO) mode, the carbon-centred radicals in mainstream cigarette smoke were trapped by TEMPO-9-AC, a carbon-centred radical probe with a low fluorescence intensity. Then the latter was transformed to a stable diamagnetic o-alkoxyamine, a high-fluorescence compound. Finally, high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was used to demonstrate the structures of the carbon-centred radicals, and high performance liquid chromatography with a fluorescence detector (HPLC-FLD) was used to determine the concentration of the carbon-centred radicals. The results showed that the 10 carbon-centred radicals were detected in the mainstream cigarette smoke, and the total carbon-centred radicals concentrations for 1R5F, 3R4F, CM6, and two Virginia type cigarettes, were 52.5 nmol/cig, 214.6 nmol/cig, 424.1 nmol/cig, 68.6 nmol/cig, and 334.2 nmol/cig, respectively; and there was positive relation between the concentrations of the total amount of carbon-centred radicals and the tar amounts in the mainstream cigarette smoke. The detection limit was 0.318 nmol/cig, and the relative standard deviations (RSDs) ranged from 3.5% to 9.7%. This method is suitable for the determination of the carbon-centred radicals in the mainstream cigarette smoke. PMID:23016293

  3. The energetic and chemical fingerprints of persistent soil organic carbon

    NASA Astrophysics Data System (ADS)

    Barré, Pierre; Plante, Alain F.; Cécillon, Lauric; Lutfalla, Suzanne; Baudin, François; Bernard, Sylvain; Christensen, Bent T.; Fernandez, Jose M.; Houot, Sabine; Kätterer, Thomas; Macdonald, Andy; van Oort, Folkert; Le Guillou, Corentin; Chenu, Claire

    2016-04-01

    A better understanding of soil organic carbon (SOC) persistence is needed to better predict SOC vulnerability to global change. The absence of convincing physical or chemical procedures to define, characterize or isolate relatively labile versus persistent SOC pools makes the study of persistent SOC difficult. Long-term bare fallow (LTBF) experiments, in which C inputs have been stopped for several decades, provide a unique opportunity to study persistent SOC without the inherent artefacts induced by extraction procedures, the hypothesis being that SOC is gradually enriched in persistent C with time as labile components decompose. We determined the evolution of thermal and chemical characteristics of bulk SOC in five LTBF experiments across Europe: Askov (DK), Grignon (FR), Rothamsted (UK), Ultuna (SW) and Versailles (FR), using a multi-technique approach involving Rock-Eval pyrolysis, thermogravimetry and differential scanning calorimetry (TG-DSC), mid-infrared diffuse reflectance spectroscopy (DRIFT-MIRS), and Near Edge X-Ray Absorption Fine Structure (NEXAFS). Results of Rock-Eval and TG analyses showed that the temperature needed to combust the SOC increased with bare fallow duration at all sites. Conversely, SOC energy density (in mJ mg-1 C) measured by DSC decreased with bare fallow duration. Rock-Eval pyrolysis results showed that hydrogen index (HI) tended to decrease with bare fallow duration whereas the oxygen index (OI) did not show consistent trends across sites. NEXAFS signals presented little differences and were dominated by carboxyl peak. Nonetheless, NEXAFS results showed a trend of increasing carboxyl groups and decreasing ketone and amide groups with bare fallow duration. Due to the mineral matrix, only a reduced part of the DRIFT-MIRS signals has been used. We observed that the bulk chemistry of aliphatic SOC (CH3 vs. CH2 functional groups) showed different trends for the different sites. Our results showed that in spite of the heterogeneity of

  4. Geomorphic controls on riparian zone hydrology, carbon pools and fluxes of dissolved organic carbon

    NASA Astrophysics Data System (ADS)

    Grabs, T.; Ledesma, J.; Laudon, H.; Seibert, J.; Kohler, S. J.; Bishop, K. H.

    2014-12-01

    Near stream (riparian) zones are an important link between terrestrial and aquatic ecosystems and influence a wide range of processes including solute transport or hydrologic behavior of headwater catchments. Understanding the links between geomorphology and riparian soils, vegetation and hydrology is, thus, a prerequisite for relating small scale processes to observations at the watershed scale. Geographic information systems (GIS) have traditionally been used to study links between geomorphology and properties of terrestrial ecosystems. Applying this approach to riparian zones, however, has only recently become feasible with the availability of high-resolution digital elevation models and the new development of suitable computational methods. In this study we present links between geomorphology and riparian zone hydrology, carbon pools and fluxes of dissolved organic carbon. Geomorphometric attributes were successfully used to predict (1) riparian groundwater levels and flow pathways, (2) the size of riparian soil carbon pools, (3) the vertical variation of dissolved organic carbon (DOC) in riparian soil profiles, as well as (4) riparian carbon fluxes and turnover times.

  5. Soil Carbon Cycling - More than Changes in Soil Organic Carbon Stocks

    NASA Astrophysics Data System (ADS)

    Lorenz, K.

    2015-12-01

    Discussions about soil carbon (C) sequestration generally focus on changes in soil organic carbon (SOC) stocks. Global SOC mass in the top 1 m was estimated at about 1325 Pg C, and at about 3000 Pg C when deeper soil layers were included. However, both inorganically and organically bound carbon forms are found in soil but estimates on global soil inorganic carbon (SIC) mass are even more uncertain than those for SOC. Globally, about 947 Pg SIC may be stored in the top 1 m, and especially in arid and semi-arid regions SIC stocks can be many times great than SOC stocks. Both SIC and SOC stocks are vulnerable to management practices, and stocks may be enhanced, for example, by optimizing net primary production (NPP) by fertilization and irrigation (especially optimizing belowground NPP for enhancing SOC stocks), adding organic matter (including black C for enhancing SOC stocks), and reducing soil disturbance. Thus, studies on soil C stocks, fluxes, and vulnerability must look at both SIC and SOC stocks in soil profiles to address large scale soil C cycling.

  6. Iron-sulfur-carbon relationships in organic-carbon-rich sequences I: Cretaceous Western Interior seaway

    USGS Publications Warehouse

    Dean, W.E.; Arthur, M.A.

    1989-01-01

    Cretaceous marine strata deposited in shallow to intermediate depths in the Western Interior seaway of North America show considerable variation in organic-carbon enrichment and degree of pyrite formation. The extreme range of paleoceanographic and depositional conditions that occurred in this seaway provide a unique opportunity to examine the effects of iron-, carbon-, and sulfur-limitation on pyrite formation in one region over about 30 my. Ternary diagrams of the system Fe-S-OC, together with some measure of the reactivity of organic matter (pyrolysis hydrogen index), provide a rapid means of recognizing iron-, carbon-, and sulfur-limitation on pyrite formation in a series of samples from a single lithologic unit. Iron limitation is indicated by a concentration of data along a line of constant S/Fe ratio on a Fe-S-OC ternary diagram. Carbon limitation is indicated by a concentration of data along a line of constant S/OC ratio. Sulfur-limitation is suggested by the lack of a systematic Fe-S-OC relationship and residual organic matter that is high in abundance and reactivity. -from Authors

  7. Carbon-catalyzed gasification of organic feedstocks in supercritical water

    SciTech Connect

    Xu, X.; Matsumura, Y.; Stenberg, J.; Antal, M.J. Jr.

    1996-08-01

    Spruce wood charcoal, macadamia shell charcoal, coal activated carbon, and coconut shell activated carbon catalyze the gasification of organic compounds in supercritical water. Feedstocks studied in this paper include glycerol, glucose, cellobiose, whole biomass feedstocks (depithed bagasse liquid extract and sewage sludge), and representative Department of Defense (DoD) wastes (methanol, methyl ethyl ketone, ethylene glycol, acetic acid, and phenol). The effects of temperature, pressure, reactant concentration, weight hourly space velocity, and the type of catalyst on the gasification of glucose are reported. Complete conversion of glucose (22% by weight in water) to a hydrogen-rich synthesis gas was realized at a weight hourly space velocity (WHSV) of 22.2 h{sup {minus}1} in supercritical water at 600 C, 34.5 MPa. Complete conversions of the whole biomass feeds were also achieved at the same temperature and pressure. The destruction efficiencies for the representative DoD wastes were also high. Deactivation of the carbon catalyst was observed after 4 h of operation without swirl in the entrance region of the reactor, but the carbon gasification efficiency remained near 100% for more than 6 h when a swirl generator was employed in the entrance of the reactor.

  8. Distribution of soil organic carbon in the conterminous United States

    USGS Publications Warehouse

    Bliss, Norman B.; Waltman, Sharon W.; West, Larry T.; Neale, Anne; Mehaffey, Megan

    2014-01-01

    The U.S. Soil Survey Geographic (SSURGO) database provides detailed soil mapping for most of the conterminous United States (CONUS). These data have been used to formulate estimates of soil carbon stocks, and have been useful for environmental models, including plant productivity models, hydrologic models, and ecological models for studies of greenhouse gas exchange. The data were compiled by the U.S. Department of Agriculture Natural Resources Conservation Service (NRCS) from 1:24,000-scale or 1:12,000-scale maps. It was found that the total soil organic carbon stock in CONUS to 1 m depth is 57 Pg C and for the total profile is 73 Pg C, as estimated from SSURGO with data gaps filled from the 1:250,000-scale Digital General Soil Map. We explore the non-linear distribution of soil carbon on the landscape and with depth in the soil, and the implications for sampling strategies that result from the observed soil carbon variability.

  9. The soil organic carbon content of anthropogenically altered organic soils effects the dissolved organic matter quality, but not the dissolved organic carbon concentrations

    NASA Astrophysics Data System (ADS)

    Frank, Stefan; Tiemeyer, Bärbel; Bechtold, Michel; Lücke, Andreas; Bol, Roland

    2016-04-01

    Dissolved organic carbon (DOC) is an important link between terrestrial and aquatic ecosystems. This is especially true for peatlands which usually show high concentrations of DOC due to the high stocks of soil organic carbon (SOC). Most previous studies found that DOC concentrations in the soil solution depend on the SOC content. Thus, one would expect low DOC concentrations in peatlands which have anthropogenically been altered by mixing with sand. Here, we want to show the effect of SOC and groundwater level on the quantity and quality of the dissolved organic matter (DOM). Three sampling sites were installed in a strongly disturbed bog. Two sites differ in SOC (Site A: 48%, Site B: 9%) but show the same mean annual groundwater level of 15 and 18 cm below ground, respectively. The SOC content of site C (11%) is similar to Site B, but the groundwater level is much lower (-31 cm) than at the other two sites. All sites have a similar depth of the organic horizon (30 cm) and the same land-use (low-intensity sheep grazing). Over two years, the soil solution was sampled bi-weekly in three depths (15, 30 and 60 cm) and three replicates. All samples were analyzed for DOC and selected samples for dissolved organic nitrogen (DON) and delta-13C and delta-15N. Despite differences in SOC and groundwater level, DOC concentrations did not differ significantly (A: 192 ± 62 mg/L, B: 163 ± 55 mg/L and C: 191 ± 97 mg/L). At all sites, DOC concentrations exceed typical values for peatlands by far and emphasize the relevance even of strongly disturbed organic soils for DOC losses. Individual DOC concentrations were controlled by the temperature and the groundwater level over the preceding weeks. Differences in DOM quality were clearer. At site B with a low SOC content, the DOC:DON ratio of the soil solution equals the soil's C:N ratio, but the DOC:DON ratio is much higher than the C:N ratio at site A. In all cases, the DOC:DON ratio strongly correlates with delta-13C. There is no

  10. Growth versus metabolic tissue replacement in mouse tissues determined by stable carbon and nitrogen isotope analysis

    NASA Astrophysics Data System (ADS)

    Macavoy, S. E.; Jamil, T.; Macko, S. A.; Arneson, L. S.

    2003-12-01

    Stable isotope analysis is becoming an extensively used tool in animal ecology. The isotopes most commonly used for analysis in terrestrial systems are those of carbon and nitrogen, due to differential carbon fractionation in C3 and C4 plants, and the approximately 3‰ enrichment in 15N per trophic level. Although isotope signatures in animal tissues presumably reflect the local food web, analysis is often complicated by differential nutrient routing and fractionation by tissues, and by the possibility that large organisms are not in isotopic equilibrium with the foods available in their immediate environment. Additionally, the rate at which organisms incorporate the isotope signature of a food through both growth and metabolic tissue replacement is largely unknown. In this study we have assessed the rate of carbon and nitrogen isotopic turnover in liver, muscle and blood in mice following a diet change. By determining growth rates, we were able to determine the proportion of tissue turnover caused by growth versus that caused by metabolic tissue replacement. Growth was found to account for approximately 10% of observed tissue turnover in sexually mature mice (Mus musculus). Blood carbon was found to have the shortest half-life (16.9 days), followed by muscle (24.7 days). Liver carbon turnover was not as well described by the exponential decay equations as other tissues. However, substantial liver carbon turnover was observed by the 28th day after diet switch. Surprisingly, these tissues primarily reflect the carbon signature of the protein, rather than carbohydrate, source in their diet. The nitrogen signature in all tissues was enriched by 3 - 5‰ over their dietary protein source, depending on tissue type, and the isotopic turnover rates were comparable to those observed in carbon.

  11. Calcium isotope evidence for suppression of carbonate dissolution in carbonate-bearing organic-rich sediments

    NASA Astrophysics Data System (ADS)

    Turchyn, Alexandra V.; DePaolo, Donald J.

    2011-11-01

    Pore fluid calcium isotope, calcium concentration and strontium concentration data are used to measure the rates of diagenetic dissolution and precipitation of calcite in deep-sea sediments containing abundant clay and organic material. This type of study of deep-sea sediment diagenesis provides unique information about the ultra-slow chemical reactions that occur in natural marine sediments that affect global geochemical cycles and the preservation of paleo-environmental information in carbonate fossils. For this study, calcium isotope ratios (δ 44/40Ca) of pore fluid calcium from Ocean Drilling Program (ODP) Sites 984 (North Atlantic) and 1082 (off the coast of West Africa) were measured to augment available pore fluid measurements of calcium and strontium concentration. Both study sites have high sedimentation rates and support quantitative sulfate reduction, methanogenesis and anaerobic methane oxidation. The pattern of change of δ 44/40Ca of pore fluid calcium versus depth at Sites 984 and 1082 differs markedly from that of previously studied deep-sea Sites like 590B and 807, which are composed of nearly pure carbonate sediment. In the 984 and 1082 pore fluids, δ 44/40Ca remains elevated near seawater values deep in the sediments, rather than shifting rapidly toward the δ 44/40Ca of carbonate solids. This observation indicates that the rate of calcite dissolution is far lower than at previously studied carbonate-rich sites. The data are fit using a numerical model, as well as more approximate analytical models, to estimate the rates of carbonate dissolution and precipitation and the relationship of these rates to the abundance of clay and organic material. Our models give mutually consistent results and indicate that calcite dissolution rates at Sites 984 and 1082 are roughly two orders of magnitude lower than at previously studied carbonate-rich sites, and the rate correlates with the abundance of clay. Our calculated rates are conservative for these

  12. [Reserves and spatial distribution characteristics of soil organic carbon in Guangdong Province].

    PubMed

    Gan, Haihua; Wu, Shunhui; Fan, Xiudan

    2003-09-01

    Soil organic carbon is the main part of terrestrial carbon reservoir and important part of soil fertility. The spatial distribution and reserves of soil organic carbon are very important for studying soil carbon cycle. According to the data from the second soil survey, soil organic carbon reserves was estimated and its spatial distribution was analysed by using GIS technique. The results showed that the total amount of soil organic carbon is about 17.52 x 10(8) t. The carbon density of laterite, lateritic red soil and red soil in Guangdong Province is 8.83, 10.31, 9.15 kg.m-2, respectively; lower than the mean carbon density of China. The carbon density of yellow soil and rice soil is 12.08, 12.17 kg.m-2, respectively; higher than the mean carbon density of China. Soil carbon density is about 10.44 kg.m-2 in Guangdong. The spatial distribution characteristic of soil organic carbon density in Guangdong is that the carbon density in south Guangdong Province is higher than that in north Guangdong Province, in that soil organic carbon density in north and middle Guangdong Province is 5-10 kg.m-2 and in east Guangdong Province is 10-15 kg.m-2. Soil organic carbon density mostly vary among 5-15 kg.m-2. PMID:14733007

  13. Soil Organic Carbon and Below Ground Biomass: Development of New GLOBE Special Measurements

    NASA Technical Reports Server (NTRS)

    Levine, Elissa; Haskett, Jonathan

    1999-01-01

    A scientific consensus is building that changes in the atmospheric concentrations of radiatively active gases are changing the climate (IPCC, 1990). One of these gases CO2 has been increasing in concentration due to additions from anthropogenic sources that are primarily industrial and land use related. The soil contains a very large pool of carbon, estimated at 1550 Gt (Lal 1995) which is larger than the atmospheric and biosphere pools of carbon combined (Greenland, 1995). The flux between the soil and the atmosphere is very large, 60 Pg C/yr (Lal 1997), and is especially important because the soil can act as either a source or a sink for carbon. On any given landscape, as much as 50% of the biomass that provides the major source of carbon can be below ground. In addition, the movement of carbon in and out of the soil is mediated by the living organisms. At present, there is no widespread sampling of soil biomass in any consistent or coordinated manner. Current large scale estimates of soil carbon are limited by the number and widely dispersed nature of the data points available. A measurement of the amount of carbon in the soil would supplement existing carbon data bases as well as provide a benchmark that can be used to determine whether the soil is storing carbon or releasing it to the atmosphere. Information on the below ground biomass would be a valuable addition to our understanding of net primary productivity and standing biomass. The addition of these as special measurements within GLOBE would be unique in terms of areal extent and continuity, and make a real contribution to scientific understanding of carbon dynamics.

  14. EFFECT OF OZONATED WATER ON THE ASSIMILABLE ORGANIC CARBON AND COLIFORM GROWTH RESPONSE VALUES AND ON PATHOGENIC BACTERIA SURVIVAL

    EPA Science Inventory

    The assimilable organic carbon (AOC) and coliform growth response (CGR) are bioassays used to determine water quality. AOC and CGR are better indexes in determining whether water can support the growth of bacteria than biological oxygen demand (BOD). The AOC value of reconditione...

  15. Dissolved Organic Carbon in the North Atlantic Meridional Overturning Circulation.

    PubMed

    Fontela, Marcos; García-Ibáñez, Maribel I; Hansell, Dennis A; Mercier, Herlé; Pérez, Fiz F

    2016-01-01

    The quantitative role of the Atlantic Meridional Overturning Circulation (AMOC) in dissolved organic carbon (DOC) export is evaluated by combining DOC measurements with observed water mass transports. In the eastern subpolar North Atlantic, both upper and lower limbs of the AMOC transport high-DOC waters. Deep water formation that connects the two limbs of the AMOC results in a high downward export of non-refractory DOC (197 Tg-C·yr(-1)). Subsequent remineralization in the lower limb of the AMOC, between subpolar and subtropical latitudes, consumes 72% of the DOC exported by the whole Atlantic Ocean. The contribution of DOC to the carbon sequestration in the North Atlantic Ocean (62 Tg-C·yr(-1)) is considerable and represents almost a third of the atmospheric CO2 uptake in the region. PMID:27240625

  16. Dissolved Organic Carbon in the North Atlantic Meridional Overturning Circulation

    PubMed Central

    Fontela, Marcos; García-Ibáñez, Maribel I.; Hansell, Dennis A.; Mercier, Herlé; Pérez, Fiz F.

    2016-01-01

    The quantitative role of the Atlantic Meridional Overturning Circulation (AMOC) in dissolved organic carbon (DOC) export is evaluated by combining DOC measurements with observed water mass transports. In the eastern subpolar North Atlantic, both upper and lower limbs of the AMOC transport high-DOC waters. Deep water formation that connects the two limbs of the AMOC results in a high downward export of non-refractory DOC (197 Tg-C·yr−1). Subsequent remineralization in the lower limb of the AMOC, between subpolar and subtropical latitudes, consumes 72% of the DOC exported by the whole Atlantic Ocean. The contribution of DOC to the carbon sequestration in the North Atlantic Ocean (62 Tg-C·yr−1) is considerable and represents almost a third of the atmospheric CO2 uptake in the region. PMID:27240625

  17. A molecular organic carbon isotope record of miocene climate changes.

    PubMed

    Schoell, M; Schouten, S; Damsté, J S; de Leeuw, J W; Summons, R E

    1994-02-25

    The difference in carbon-13 ((13)C) contents of hopane and sterane biomarkers in the Monterey formation (Naples Beach, California) parallels the Miocene inorganic record of the change in (18)O (delta(18)O), reflecting the Miocene evolution from a well-mixed to a highly stratified photic zone (upper 100 meters) in the Pacific. Steranes (delta(13)C = 25.4 +/- 0.7 per mil versus the Pee Dee belemnite standard) from shallow photic-zone organisms do not change isotopically throughout the Miocene. In contrast, sulfur-bound C(35) hopanes (likely derived from bacterial plankton living at the base of the photic zone) have systematically decreasing (13)C concentrations in Middle and Late Miocene samples (delta(13)C = -29.5 to -31.5 per mil), consistent with the Middle Miocene formation of a carbon dioxide-rich cold water mass at the base of the photic zone. PMID:17831625

  18. Dissolved Organic Carbon in the North Atlantic Meridional Overturning Circulation

    NASA Astrophysics Data System (ADS)

    Fontela, Marcos; García-Ibáñez, Maribel I.; Hansell, Dennis A.; Mercier, Herlé; Pérez, Fiz F.

    2016-05-01

    The quantitative role of the Atlantic Meridional Overturning Circulation (AMOC) in dissolved organic carbon (DOC) export is evaluated by combining DOC measurements with observed water mass transports. In the eastern subpolar North Atlantic, both upper and lower limbs of the AMOC transport high-DOC waters. Deep water formation that connects the two limbs of the AMOC results in a high downward export of non-refractory DOC (197 Tg-C·yr‑1). Subsequent remineralization in the lower limb of the AMOC, between subpolar and subtropical latitudes, consumes 72% of the DOC exported by the whole Atlantic Ocean. The contribution of DOC to the carbon sequestration in the North Atlantic Ocean (62 Tg-C·yr‑1) is considerable and represents almost a third of the atmospheric CO2 uptake in the region.

  19. Sulfur and carbon cycling in organic-rich marine sediments

    NASA Technical Reports Server (NTRS)

    Martens, C. S.

    1985-01-01

    Nearshore, continental shelf, and slope sediments are important sites of microbially mediated carbon and sulfur cycling. Marine geochemists investigated the rates and mechanisms of cycling processes in these environments by chemical distribution studies, in situ rate measurements, and steady state kinetic modeling. Pore water chemical distributions, sulfate reduction rates, and sediment water chemical fluxes were used to describe cycling on a ten year time scale in a small, rapidly depositing coastal basin, Cape Lookout Bight, and at general sites on the upper continental slope off North Carolina, U.S.A. In combination with 210 Pb sediment accumulation rates, these data were used to establish quantitative carbon and sulfur budgets as well as the relative importance of sulfate reduction and methanogeneis as the last steps in the degradation of organic matter.

  20. Self-organized global control of carbon emissions

    NASA Astrophysics Data System (ADS)

    Zhao, Zhenyuan; Fenn, Daniel J.; Hui, Pak Ming; Johnson, Neil F.

    2010-09-01

    There is much disagreement concerning how best to control global carbon emissions. We explore quantitatively how different control schemes affect the collective emission dynamics of a population of emitting entities. We uncover a complex trade-off which arises between average emissions (affecting the global climate), peak pollution levels (affecting citizens’ everyday health), industrial efficiency (affecting the nation’s economy), frequency of institutional intervention (affecting governmental costs), common information (affecting trading behavior) and market volatility (affecting financial stability). Our findings predict that a self-organized free-market approach at the level of a sector, state, country or continent can provide better control than a top-down regulated scheme in terms of market volatility and monthly pollution peaks. The control of volatility also has important implications for any future derivative carbon emissions market.

  1. [Effects of climate change on forest soil organic carbon storage: a review].

    PubMed

    Zhou, Xiao-yu; Zhang, Cheng-yi; Guo, Guang-fen

    2010-07-01

    Forest soil organic carbon is an important component of global carbon cycle, and the changes of its accumulation and decomposition directly affect terrestrial ecosystem carbon storage and global carbon balance. Climate change would affect the photosynthesis of forest vegetation and the decomposition and transformation of forest soil organic carbon, and further, affect the storage and dynamics of organic carbon in forest soils. Temperature, precipitation, atmospheric CO2 concentration, and other climatic factors all have important influences on the forest soil organic carbon storage. Understanding the effects of climate change on this storage is helpful to the scientific management of forest carbon sink, and to the feasible options for climate change mitigation. This paper summarized the research progress about the distribution of organic carbon storage in forest soils, and the effects of elevated temperature, precipitation change, and elevated atmospheric CO2 concentration on this storage, with the further research subjects discussed. PMID:20879549

  2. Estimating soil organic carbon input to marine sediments (Invited)

    NASA Astrophysics Data System (ADS)

    Weijers, J.; Schouten, S.; Schefuss, E.; Schneider, R. R.; Sinninghe Damsté, J. S.

    2009-12-01

    Estimating (past) input of terrestrial organic carbon (OC) in marine sediments is complicated due to the heterogeneity of the OC. Two end member mixing models based on different parameters often give different results. This is in part due to the fact that terrestrial OC is only represented by one end member (often representing plant OC) where it in fact consists of two OC pools, i.e., plant and soil OC. The branched vs. isoprenoid tetraether (BIT) index is a new proxy for soil OC input, with the branched tetraether membrane lipids being derived from bacteria living in soils and peat bogs [1]. We have now applied this molecular proxy in a three end member mixing model, in conjunction with d13C and C/N values of total organic matter, in a marine sediment core from the Congo deep sea fan to estimate inputs of marine, soil and plant OC to this location over the last deglaciation. Results indicate an average of 45% of the OC being of soil origin, pointing to the importance of soil OC and the need for proper characterization of this fraction. [1] Hopmans et al. (2004) EPSL 224, 107-116. Figure 1: Composition of the organic carbon input to the Congo deep sea fan over the last 20 thousand years. YD = Younger Dryas; LGM = Last Glacial Maximum

  3. Determination of optimum electrolyte composition for molten carbonate fuel cells

    SciTech Connect

    Yuh, C.Y.; Pigeaud, A.

    1987-01-01

    The objective of this study is to determine the optimum electrolyte composition for molten carbonate fuel cells. To accomplish this, the contractor will provide: (1) Comprehensive reports of on-going efforts to optimize carbonate composition. (2) A list of characteristics affected by electrolyte composition variations (e.g. ionic conductivity, vapor pressure, melting range, gas solubility, exchange current densities on NiO, corrosion and cathode dissolution effects). (3) Assessment of the overall effects that these characteristics have state-of-the-art cell voltage and lifetime.

  4. Determination of the intershell conductance in a multiwall carbon nanotube

    NASA Astrophysics Data System (ADS)

    Stetter, A.; Vancea, J.; Back, C. H.

    2008-10-01

    We have measured the current induced voltage drop along an individual multiwall carbon nanotube as a function of the distance to the current injecting electrode. The measurements have been performed at room temperature using scanning probe potentiometry combined with scanning electron microscopy. For a nanotube with an incomplete outer shell, a sharp potential jump was observed at the end of the outermost shell. The electric potential variation along the carbon nanotube has been used to determine the contact resistance between metal electrodes and the tube, the intrashell resistance, and the intershell conductance.

  5. Ultrasonic determination of carbon content in uranium metal

    NASA Astrophysics Data System (ADS)

    Poncelow, J.; Morrell, J.; Olson, D. L.; Mishra, B.

    2012-05-01

    A nondestructive method to determine solute content of carbon in polycrystalline uranium by ultrasonic techniques is currently being developed. The problem is approached by considering first theories developed in the field of physical acoustics applicable to variation in attenuation and elasticity with respect to interstitial and second-phase contents. Attention is given to the physical metallurgy of uranium, specifically phase stability and the effects of carbon concentration on physical properties. Experimental verification of theory is provided using Resonant Ultrasound Spectroscopy (RUS) and pulse-echo time of flight measurements, the former yielding elastic moduli and quality factors and the latter supplying attenuation and velocity information.

  6. Effect of organic fertilizer and biochar application on soil macro-aggregate formation and organic carbon turnover

    NASA Astrophysics Data System (ADS)

    Grunwald, Dennis; Kaiser, Michael; Ludwig, Bernard

    2015-04-01

    Macro-aggregates are important for the organic matter dynamic and thus the productivity of sustainably managed soils. To date, less is known about the influence of biochar in comparison to other commonly used organic soil additives on the formation of macro-aggregates and organic carbon turnover. Here we aimed to analyze the effects of biochar applied individually and in combination with slurry versus the effects of the individual application of slurry and manure on macro-aggregate yield, the associated organic carbon concentration, and the organic carbon mineralization. For this, we crushed the macro-aggregate fraction (>250 μm) of two different soils that were then mixed with biochar (combustion temperature: 550° C, feedstock: woodchips) and/or cattle-slurry or cattle-manure and incubated within a microcosm experiment at 5° C, 15° C, and 25° C. We monitored the CO2 evolution during the incubation experiment. After four and eight weeks, we determined the dry mass and the carbon concentration of the newly formed macro-aggregates (>250 μm) and the microbial biomass carbon concentration. Carbon mineralization was modelled assuming first-order kinetics and using a rate modifying factor for the temperature (taken from the RothC-26.3 model). Two pools were considered (mineralization of the native organic matter from the control soils and mineralization of the substrates added) in each treatment and the models were calibrated to the C mineralization data at 25° C, whereas the data for 15° C and 5° C were used for validation. Independent from the incubation temperature and the duration of the experiment, the individual application of biochar did not show significant effects on the macro-aggregate yield, the associated carbon concentration, or the CO2 emission rate compared to the control sample receiving no amendments. For the application of biochar in combination with slurry, we observed only for the 15° C treatment higher CO2 emission rates in combination with

  7. Assessment of relative accuracy in the determination of organic matter concentrations in aquatic systems

    USGS Publications Warehouse

    Aiken, G.; Kaplan, L.A.; Weishaar, J.

    2002-01-01

    Accurate determinations of total (TOC), dissolved (DOC) and particulate (POC) organic carbon concentrations are critical for understanding the geochemical, environmental, and ecological roles of aquatic organic matter. Of particular significance for the drinking water industry, TOC measurements are the basis for compliance with US EPA regulations. The results of an interlaboratory comparison designed to identify problems associated with the determination of organic matter concentrations in drinking water supplies are presented. The study involved 31 laboratories and a variety of commercially available analytical instruments. All participating laboratories performed well on samples of potassium hydrogen phthalate (KHP), a compound commonly used as a standard in carbon analysis. However, problems associated with the oxidation of difficult to oxidize compounds, such as dodecylbenzene sulfonic acid and caffeine, were noted. Humic substances posed fewer problems for analysts. Particulate organic matter (POM) in the form of polystyrene beads, freeze-dried bacteria and pulverized leaf material were the most difficult for all analysts, with a wide range of performances reported. The POM results indicate that the methods surveyed in this study are inappropriate for the accurate determination of POC and TOC concentration. Finally, several analysts had difficulty in efficiently separating inorganic carbon from KHP solutions, thereby biasing DOC results.

  8. Organic carbon decomposition rates controlled by water retention time across inland waters

    NASA Astrophysics Data System (ADS)

    Catalán, Núria; Marcé, Rafael; Kothawala, Dolly N.; Tranvik, Lars. J.

    2016-07-01

    The loss of organic carbon during passage through the continuum of inland waters from soils to the sea is a critical component of the global carbon cycle. Yet, the amount of organic carbon mineralized and released to the atmosphere during its transport remains an open question, hampered by the absence of a common predictor of organic carbon decay rates. Here we analyse a compilation of existing field and laboratory measurements of organic carbon decay rates and water residence times across a wide range of aquatic ecosystems and climates. We find a negative relationship between the rate of organic carbon decay and water retention time across systems, entailing a decrease in organic carbon reactivity along the continuum of inland waters. We find that the half-life of organic carbon is short in inland waters (2.5 +/- 4.7 yr) compared to terrestrial soils and marine ecosystems, highlighting that freshwaters are hotspots of organic carbon degradation. Finally, we evaluate the response of organic carbon decay rates to projected changes in runoff. We calculate that regions projected to become drier or wetter as the global climate warms will experience changes in organic carbon decay rates of up to about 10%, which illustrates the influence of hydrological variability on the inland waters carbon cycle.

  9. Determination of carbon by the oxidation reduction reaction with chromium

    NASA Technical Reports Server (NTRS)

    Mashkovich, L.; Kuteynikov, A. F.

    1978-01-01

    Free carbon was determined in silicon and boron carbides in ash, oxides, and other materials by oxidation to carbon dioxide with a mixture of K2Cr2O7 + H2SO4. The determination was made from the amount of CR(6) consumed, by adding excess Mohr's salt and titrating with a standard solution of KMnO4. The amount of Cr(6) self reduced was determined in a blank test. Optimum oxidation and conditions were achieved when the volumes of 5% k2Cr2Oz and H2SO4 were equal. The mixture was boiled for 1-2 hours using a reflex condenser. The volume should not be reduced, in order to avoid an increase in the sulfuric acid concentration. The relative error was 4-7% for 0.005-0.04 g C and less than or equal to 3.5% for 0.1 g C.

  10. Organic Carbon--water Concentration Quotients (IIsocS and [pi]pocS): Measuring Apparent Chemical Disequilibria and Exploring the Impact of Black Carbon in Lake Michigan

    EPA Science Inventory

    When black carbon (bc) and biologically derived organic carbon (bioc) phases are present in sediments or suspended particulates, both forms of carbon act additively to sorb organic chemicals but the bc phase has more sorption capacity per unit mass. . . .

  11. DETERMINATION OF TOTAL ORGANIC EMISSIONS FROM HAZARDOUS WASTE COMBUSTORS

    EPA Science Inventory

    Determination of "Total Organics" from stack emissions is much more complicated am might be expected, and more published guidance is needed badly. he best scheme available for analysis of "Total Organics" of stack emissions for material balance style "bookkeeping" includes determ...

  12. Modeling the contribution of dissolved organic carbon to carbon sequestration during the last glacial maximum

    NASA Astrophysics Data System (ADS)

    Ma, Wentao; Tian, Jun

    2014-10-01

    Dissolved organic carbon (DOC) is a carbon reservoir that is as large as the atmospheric CO2 pool, and its contribution to the global carbon cycle is gaining attention. As DOC is a dissolved tracer, its distribution can serve to trace the mixing of water masses and the pathways of ocean circulation. Published proxy and model reconstructions have revealed that, during the last glacial maximum (LGM), the pattern of deep ocean circulation differed from that of the modern ocean, whereby additional carbon is assumed to have been sequestered in stratified LGM deep water. The aim of this study is to explore the distribution of DOC and its production/removal rate during the LGM using the Grid ENabled Integrated Earth system model (GENIE). Modeled results reveal that increased salinity of bottom waters in the Southern Ocean is associated with stronger stratification and oxygen depletion. The stratified LGM deep ocean traps more nutrients, resulting in a decrease in the DOC reservoir size that, in turn, causes a negative feedback for carbon sequestration. This finding requires an increase in DOC lifetime to compensate for the negative feedback. The upper limit of DOC lifetime is assumed to be 20,000 years. Modeled results derive an increase (decrease) in DOC reservoir by 100 Pg C leading to an atmospheric CO2 decrease (increase) of 9.1 ppm and a dissolved inorganic carbon δ13C increase (decrease) of 0.06‰. The DOC removal rate is estimated to be 39.5 Tg C year-1 in the deep sea during the LGM. The contribution of DOC to the LGM carbon cycle elucidates potential carbon sink-increasing strategies.

  13. Improved automation of dissolved organic carbon sampling for organic-rich surface waters.

    PubMed

    Grayson, Richard P; Holden, Joseph

    2016-02-01

    In-situ UV-Vis spectrophotometers offer the potential for improved estimates of dissolved organic carbon (DOC) fluxes for organic-rich systems such as peatlands because they are able to sample and log DOC proxies automatically through time at low cost. In turn, this could enable improved total carbon budget estimates for peatlands. The ability of such instruments to accurately measure DOC depends on a number of factors, not least of which is how absorbance measurements relate to DOC and the environmental conditions. Here we test the ability of a S::can Spectro::lyser™ for measuring DOC in peatland streams with routinely high DOC concentrations. Through analysis of the spectral response data collected by the instrument we have been able to accurately measure DOC up to 66 mg L(-1), which is more than double the original upper calibration limit for this particular instrument. A linear regression modelling approach resulted in an accuracy >95%. The greatest accuracy was achieved when absorbance values for several different wavelengths were used at the same time in the model. However, an accuracy >90% was achieved using absorbance values for a single wavelength to predict DOC concentration. Our calculations indicated that, for organic-rich systems, in-situ measurement with a scanning spectrophotometer can improve fluvial DOC flux estimates by 6 to 8% compared with traditional sampling methods. Thus, our techniques pave the way for improved long-term carbon budget calculations from organic-rich systems such as peatlands. PMID:26580726

  14. Aggregate distribution and associated organic carbon influenced by cover crops

    NASA Astrophysics Data System (ADS)

    Barquero, Irene; García-González, Irene; Benito, Marta; Gabriel, Jose Luis; Quemada, Miguel; Hontoria, Chiquinquirá

    2013-04-01

    Replacing fallow with cover crops during the non-cropping period seems to be a good alternative to diminish soil degradation by enhancing soil aggregation and increasing organic carbon. The aim of this study was to analyze the effect of replacing fallow by different winter cover crops (CC) on the aggregate distribution and C associated of an Haplic Calcisol. The study area was located in Central Spain, under semi-arid Mediterranean climate. A 4-year field trial was conducted using Barley (Hordeum vulgare L.) and Vetch (Vicia sativa L.) as CC during the intercropping period of maize (Zea mays L.) under irrigation. All treatments were equally irrigated and fertilized. Maize was directly sown over CC residues previously killed in early spring. Composite samples were collected at 0-5 and 5-20 cm depths in each treatment on autumn of 2010. Soil samples were separated by wet sieving into four aggregate-size classes: large macroaggregates ( >2000 µm); small macroaggregates (250-2000 µm); microaggregates (53-250 µm); and < 53 µm (silt + clay size). Organic carbon associated to each aggregate-size class was measured by Walkley-Black Method. Our preliminary results showed that the aggregate-size distribution was dominated by microaggregates (48-53%) and the <53 µm fraction (40-44%) resulting in a low mean weight diameter (MWD). Both cover crops increased aggregate size resulting in a higher MWD (0.28 mm) in comparison with fallow (0.20 mm) in the 0-5 cm layer. Barley showed a higher MWD than fallow also in 5-20 cm layer. Organic carbon concentrations in aggregate-size classes at top layer followed the order: large macroaggregates > small macroaggregates > microaggregates > silt + clay size. Treatments did not influence C concentration in aggregate-size classes. In conclusion, cover crops improved soil structure increasing the proportion of macroaggregates and MWD being Barley more effective than Vetch at subsurface layer.

  15. Soil organic carbon sequestration and tillage systems in Mediterranean environments

    NASA Astrophysics Data System (ADS)

    Francaviglia, Rosa; Di Bene, Claudia; Marchetti, Alessandro; Farina, Roberta

    2016-04-01

    Soil carbon sequestration is of special interest in Mediterranean areas, where rainfed cropping systems are prevalent, inputs of organic matter to soils are low and mostly rely on crop residues, while losses are high due to climatic and anthropic factors such as intensive and non-conservative farming practices. The adoption of reduced or no tillage systems, characterized by a lower soil disturbance in comparison with conventional tillage, has proved to be positively effective on soil organic carbon (SOC) conservation and other physical and chemical processes, parameters or functions, e.g. erosion, compaction, ion retention and exchange, buffering capacity, water retention and aggregate stability. Moreover, soil biological and biochemical processes are usually improved by the reduction of tillage intensity. The work deals with some results available in the scientific literature, and related to field experiment on arable crops performed in Italy, Greece, Morocco and Spain. Data were organized in a dataset containing the main environmental parameters (altitude, temperature, rainfall), soil tillage system information (conventional, minimum and no-tillage), soil parameters (bulk density, pH, particle size distribution and texture), crop type, rotation, management and length of the experiment in years, initial SOCi and final SOCf stocks. Sampling sites are located between 33° 00' and 43° 32' latitude N, 2-860 m a.s.l., with mean annual temperature and rainfall in the range 10.9-19.6° C and 355-900 mm. SOC data, expressed in t C ha‑1, have been evaluated both in terms of Carbon Sequestration Rate, given by [(SOCf-SOCi)/length in years], and as percentage change in comparison with the initial value [(SOCf-SOCi)/SOCi*100]. Data variability due to the different environmental, soil and crop management conditions that influence SOC sequestration and losses will be examined.

  16. Seqestration of dissolved organic carbon in the deep sea

    SciTech Connect

    Daniel J. Repeta

    2006-03-01

    There are 600 GT of dissolved organic carbon (DOC) sequestered in seawater. The marine inventory of DOC is set by its concentration in the deep sea, which is nearly constant at 35+2µM C, irrespective of sample location or depth. Isotopic measurements show deep sea DOC to be depleted in radiocarbon, with an apparent radiocarbon age of between 4000ybp (Atlantic) and 6000ybp (Pacific). From the radiocarbon data, we can infer that deep sea DOC is inert and does not cycle on less than millennial time scales. However, high precision DOC measurements show deep sea concentrations are variable at the + 1-2µM DOC level, suggesting a fraction of deep sea DOC, equivalent to 15-30Gt C, is cycling on short time scales, acting as a sink for new, atmospheric carbon. This project is designed to identify and quantify the biological and physical processes that sequester DOM in the deep sea by making compound specific radiocarbon measurements on sugars and proteins extracted from deep sea DOC. Our Hawaii surface seawater sample has a DIC Δ14C value of 72 + 7 ‰ and shows the influence of bomb radiocarbon on surface water DIC values. HMWDOC Δ14C is 10 ‰, significantly depleted in radiocarbon relative to DIC. Purification of HMWDOC by reverse phase HPLC yields seven neutral sugars with radiocarbon values of 47 – 67‰. Assuming the radiocarbon determinations of individual sugars in HMWDOC serve as replicates, then the average Δ14C for neutral sugars in HMWDOC is 57 + 6 ‰(1 SD, n=11), only slightly depleted in 14C relative to DIC. There has been a sharp decrease in radiocarbon values for DIC in the North Pacific Ocean over the past few decades. If neutral sugars cycle more slowly than DIC, we would expect them to have correspondingly higher radiocarbon values. Previous studies have modeled upper ocean DOC as a two component mixture of newly synthesized DOC with a radiocarbon value equal to DIC, and an old component with a radiocarbon value equal to deep sea DO14C. In order to

  17. Natural versus wastewater derived dissolved organic carbon: implications for the environmental fate of organic micropollutants.

    PubMed

    Neale, Peta A; Antony, Alice; Gernjak, Wolfgang; Leslie, Greg; Escher, Beate I

    2011-08-01

    The interaction of organic micropollutants with dissolved organic carbon (DOC) can influence their transport, degradation and bioavailability. While this has been well established for natural organic carbon, very little is known regarding the influence of DOC on the fate of micropollutants during wastewater treatment and water recycling. Dissolved organic carbon-water partition coefficients (K(DOC)) for wastewater derived and reference DOC were measured for a range of micropollutants using a depletion method with polydimethylsiloxane disks. For micropollutants with an octanol-water partition coefficient (log K(OW)) greater than 4 there was a significant difference in K(DOC) between reference and wastewater derived DOC, with partitioning to wastewater derived DOC over 1000 times lower for the most hydrophobic micropollutants. The interaction of nonylphenol with wastewater derived DOC from different stages of a wastewater and advanced water treatment train was studied, but little difference in K(DOC) was observed. Organic carbon characterisation revealed that reference and wastewater derived DOC had very different properties due to their different origins. Consequently, the reduced sorption capacity of wastewater derived DOC may be related to their microbial origin which led to reduced aromaticity and lower molecular weight. This study suggests that for hydrophobic micropollutants (log K(OW) > 4) a higher concentration of freely dissolved and thus bioavailable micropollutants is expected in the presence of wastewater derived DOC than predicted using K(DOC) values quantified using reference DOC. The implication is that naturally derived DOC may not be an appropriate surrogate for wastewater derived DOC as a matrix for assessing the fate of micropollutants in engineered systems. PMID:21703657

  18. Adsorption of organic contaminants by graphene nanosheets, carbon nanotubes and granular activated carbons under natural organic matter preloading conditions.

    PubMed

    Ersan, Gamze; Kaya, Yasemin; Apul, Onur G; Karanfil, Tanju

    2016-09-15

    The effect of NOM preloading on the adsorption of phenanthrene (PNT) and trichloroethylene (TCE) by pristine graphene nanosheets (GNS) and graphene oxide nanosheet (GO) was investigated and compared with those of a single-walled carbon nanotube (SWCNT), a multi-walled carbon nanotube (MWCNT), and two coal based granular activated carbons (GACs). PNT uptake was higher than TCE by all adsorbents on both mass and surface area bases. This was attributed to the hydrophobicity of PNT. The adsorption capacities of PNT and TCE depend on the accessibility of the organic molecules to the inner regions of the adsorbent which was influenced from the molecular size of OCs. The adsorption capacities of all adsorbents decreased as a result of NOM preloading due to site competition and/or pore/interstice blockage. However, among all adsorbents, GO was generally effected least from the NOM preloading for PNT, whereas there was not observed any trend of NOM competition with a specific adsorbent for TCE. In addition, SWCNT was generally affected most from the NOM preloading for TCE and there was not any trend for PNT. The overall results indicated that the fate and transport of organic contaminants by GNSs and CNTs type of nanoadsorbents and GACs in different natural systems will be affected by water quality parameters, characteristics of adsorbent, and properties of adsorbate. PMID:27107611

  19. Electrochemically gated organic photovoltaic with tunable carbon nanotube cathodes

    NASA Astrophysics Data System (ADS)

    Cook, Alexander B.; Yuen, Jonathan D.; Zakhidov, Anvar

    2013-10-01

    We demonstrate an organic photovoltaic (OPV) device with an electrochemically gated carbon nanotube (CNT) charge collector. Bias voltages applied to the gate electrode reconfigure the common CNT electrode from an anode into a cathode which effectively collects photogenerated electrons, dramatically increasing all solar cell parameters to achieve a power conversion efficiency of ˜3%. This device requires very little current to initially charge and the leakage current is negligible compared to the photocurrent. This device can also be viewed as a hybrid tandem OPV-supercapacitor with a common CNT electrode. Other regimes of operation are briefly discussed.

  20. Young organic matter as a source of carbon dioxide outgassing from Amazonian rivers

    SciTech Connect

    Mayorga, E; Aufdenkampe, A K; Masiello, C A; Krusche, A V; Hedges, J I; Quay, P D; Richey, J E; Brown, T A

    2005-06-23

    Rivers are generally supersaturated with respect to carbon dioxide, resulting in large gas evasion fluxes that can be a significant component of regional net carbon budgets. Amazonian rivers were recently shown to outgas more than ten times the amount of carbon exported to the ocean in the form of total organic carbon or dissolved inorganic carbon. High carbon dioxide concentrations in rivers originate largely from in situ respiration of organic carbon, but little agreement exists about the sources or turnover times of this carbon. Here we present results of an extensive survey of the carbon isotope composition ({sup 13}C and {sup 14}C) of dissolved inorganic carbon and three size-fractions of organic carbon across the Amazonian river system. We find that respiration of contemporary organic matter (less than 5 years old) originating on land and near rivers is the dominant source of excess carbon dioxide that drives outgassing in mid-size to large rivers, although we find that bulk organic carbon fractions transported by these rivers range from tens to thousands of years in age. We therefore suggest that a small, rapidly cycling pool of organic carbon is responsible for the large carbon fluxes from land to water to atmosphere in the humid tropics.

  1. Adsorption uptake of synthetic organic chemicals by carbon nanotubes and activated carbons

    NASA Astrophysics Data System (ADS)

    Brooks, A. J.; Lim, Hyung-nam; Kilduff, James E.

    2012-07-01

    Carbon nanotubes (CNTs) have shown great promise as high performance materials for adsorbing priority pollutants from water and wastewater. This study compared uptake of two contaminants of interest in drinking water treatment (atrazine and trichloroethylene) by nine different types of carbonaceous adsorbents: three different types of single walled carbon nanotubes (SWNTs), three different sized multi-walled nanotubes (MWNTs), two granular activated carbons (GACs) and a powdered activated carbon (PAC). On a mass basis, the activated carbons exhibited the highest uptake, followed by SWNTs and MWNTs. However, metallic impurities in SWNTs and multiple walls in MWNTs contribute to adsorbent mass but do not contribute commensurate adsorption sites. Therefore, when uptake was normalized by purity (carbon content) and surface area (instead of mass), the isotherms collapsed and much of the CNT data was comparable to the activated carbons, indicating that these two characteristics drive much of the observed differences between activated carbons and CNT materials. For the limited data set here, the Raman D:G ratio as a measure of disordered non-nanotube graphitic components was not a good predictor of adsorption from solution. Uptake of atrazine by MWNTs having a range of lengths and diameters was comparable and their Freundlich isotherms were statistically similar, and we found no impact of solution pH on the adsorption of either atrazine or trichloroethylene in the range of naturally occurring surface water (pH = 5.7-8.3). Experiments were performed using a suite of model aromatic compounds having a range of π-electron energy to investigate the role of π-π electron donor-acceptor interactions on organic compound uptake by SWNTs. For the compounds studied, hydrophobic interactions were the dominant mechanism in the uptake by both SWNTs and activated carbon. However, comparing the uptake of naphthalene and phenanthrene by activated carbon and SWNTs, size exclusion effects

  2. Adsorption uptake of synthetic organic chemicals by carbon nanotubes and activated carbons.

    PubMed

    Brooks, A J; Lim, Hyung-nam; Kilduff, James E

    2012-07-27

    Carbon nanotubes (CNTs) have shown great promise as high performance materials for adsorbing priority pollutants from water and wastewater. This study compared uptake of two contaminants of interest in drinking water treatment (atrazine and trichloroethylene) by nine different types of carbonaceous adsorbents: three different types of single walled carbon nanotubes (SWNTs), three different sized multi-walled nanotubes (MWNTs), two granular activated carbons (GACs) and a powdered activated carbon (PAC). On a mass basis, the activated carbons exhibited the highest uptake, followed by SWNTs and MWNTs. However, metallic impurities in SWNTs and multiple walls in MWNTs contribute to adsorbent mass but do not contribute commensurate adsorption sites. Therefore, when uptake was normalized by purity (carbon content) and surface area (instead of mass), the isotherms collapsed and much of the CNT data was comparable to the activated carbons, indicating that these two characteristics drive much of the observed differences between activated carbons and CNT materials. For the limited data set here, the Raman D:G ratio as a measure of disordered non-nanotube graphitic components was not a good predictor of adsorption from solution. Uptake of atrazine by MWNTs having a range of lengths and diameters was comparable and their Freundlich isotherms were statistically similar, and we found no impact of solution pH on the adsorption of either atrazine or trichloroethylene in the range of naturally occurring surface water (pH = 5.7-8.3). Experiments were performed using a suite of model aromatic compounds having a range of π-electron energy to investigate the role of π-π electron donor-acceptor interactions on organic compound uptake by SWNTs. For the compounds studied, hydrophobic interactions were the dominant mechanism in the uptake by both SWNTs and activated carbon. However, comparing the uptake of naphthalene and phenanthrene by activated carbon and SWNTs, size exclusion effects

  3. Determination of the atherogenic potential of inhaled carbon monoxide

    SciTech Connect

    Penn, A. )

    1993-05-01

    he effects of chronic exposure to moderate levels of carbon monoxide upon the augmentation of arteriosclerotic plaque development were investigated in a series of in vivo studies in the cockerel (young rooster). This animal model has been well characterized, especially regarding the role of environmental agents in exacerbating early stages of plaque development. Cockerels injected with subtumorigenic doses of carcinogens exhibit markedly accelerated development of aortic arteriosclerotic plaques. Inhalation of mainstream smoke from two packs of cigarettes (100 minutes/day for 16 weeks) causes small but statistically significant increases in plaque size. As is the case with many animal models of plaque development, raised fat-proliferative plaques also appear in these animals following cholesterol feeding. Carbon monoxide is a ubiquitous pollutant in urban environments, where it is derived largely from mobile sources and cigarette smoke. Exposure to chronically elevated carbon monoxide levels has been implicated in a number of health-related problems. Whether such exposure plays a role in the development of arteriosclerosis has not been determined conclusively. In the present study, three questions were posed: 1. Will inhaled carbon monoxide at levels of 50 to 200 parts per million (ppm)* (two hours/day for 16 weeks) be sufficient to augment arteriosclerotic plaque development in cockerels, in the absence of other plaque-promoting agents 2. Will the inhalation of 100 ppm carbon monoxide (two hours/day for 16 weeks), concomitant with the feeding of low levels (0.1%) of cholesterol, yield larger plaques than those obtained with either of these agents administered alone 3. Will inhalation of 100 ppm carbon monoxide (two hours/day for 11 or 22 weeks), by cockerels in whom plaques have already appeared, further augment plaque development Cockerels were exposed to carefully regulated levels of carbon monoxide in stainless-steel and Plexiglas dynamic exposure chambers.

  4. Dispersion of organic pigments using supercritical carbon dioxide.

    PubMed

    Cheng, W T; Hsu, C W; Chih, Y W

    2004-02-01

    This research describes dispersion of organic pigments using supercritical fluids. With low surface tension and high diffusivity of fluids in supercritical states, aggregated particles may be effectively wetted and swelled to form the primary constituent of the dispersing solution by volume. In this paper, the conditions of temperature and pressure are used to control the density of supercritical carbon dioxide subject to PGMEA as cosolvent for dispersing organic powder in a solution. As shown from measurement with a laser scattering particle analyzer, the average diameter of phthalocyanine green 36 with the haloid structure can be significantly reduced to 93.5 nm; for aminoanthraquinone red containing and amino group (-NH(2)) and phthalocyanine blue 15:6 with symmetry benzene and inner hydrogen bond, the mean particle sizes are 178.5 and 188.7 nm, respectively, using supercritical CO(2). Additionally, the transmittance of UV light is used to confirm the dispersing performance in this study. PMID:14693141

  5. Space Station Freedom Water Recovery test total organic carbon accountability

    NASA Technical Reports Server (NTRS)

    Davidson, Michael W.; Slivon, Laurence; Sheldon, Linda; Traweek, Mary

    1991-01-01

    Marshall Space Flight Center's (MSFC) Water Recovery Test (WRT) addresses the concept of integrated hygiene and potable reuse water recovery systems baselined for Space Station Freedom (SSF). To assess the adequacy of water recovery system designs and the conformance of reclaimed water quality to established specifications, MSFC has initiated an extensive water characterization program. MSFC's goal is to quantitatively account for a large percentage of organic compounds present in waste and reclaimed hygiene and potable waters from the WRT and in humidity condensate from Spacelab missions. The program is coordinated into Phase A and B. Phase A's focus is qualitative and semi-quantitative. Precise quantitative analyses are not emphasized. Phase B's focus centers on a near complete quantitative characterization of all water types. Technical approaches along with Phase A and partial Phase B investigations on the compositional analysis of Total Organic Carbon (TOC) Accountability are presented.

  6. Organic Matter Stabilization in Soil Microaggregates: Implications from Spatial Heterogeneity of Organic Carbon Contents and Carbon Forms

    SciTech Connect

    Lehmann,J.; Kinyangi, J.; Solomon, D.

    2007-01-01

    This study investigates the spatial distribution of organic carbon (C) in free stable microaggregates (20-250 {mu}m; not encapsulated within macroaggregates) from one Inceptisol and two Oxisols in relation to current theories of the mechanisms of their formation. Two-dimensional micro- and nano-scale observations using synchrotron-based Fourier-transform infrared (FTIR) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy yielded maps of the distribution of C amounts and chemical forms. Carbon deposits were unevenly distributed within microaggregates and did not show any discernable gradients between interior and exterior of aggregates. Rather, C deposits appeared to be patchy within the microaggregates. In contrast to the random location of C, there were micron-scale patterns in the spatial distribution of aliphatic C-H (2922 cm-1), aromatic C=C and N-H (1589 cm-1) and polysaccharide C-O (1035 cm-1). Aliphatic C forms and the ratio of aliphatic C/aromatic C were positively correlated (r 2 of 0.66-0.75 and 0.27-0.59, respectively) to the amount of O-H on kaolinite surfaces (3695 cm-1), pointing at a strong role for organo-mineral interactions in C stabilization within microaggregates and at a possible role for molecules containing aliphatic C-H groups in such interactions. This empirical relationship was supported by nanometer-scale observations using NEXAFS which showed that the organic matter in coatings on mineral surfaces had more aliphatic and carboxylic C with spectral characteristics resembling microbial metabolites than the organic matter of the entire microaggregate. Our observations thus support models of C stabilization in which the initially dominant process is adsorption of organics on mineral surfaces rather than occlusion of organic debris by adhering clay particles.

  7. Simplified method to assess soil organic matter in landscape and carbon sequestration studies

    NASA Astrophysics Data System (ADS)

    Pallasser, Robert; Minasny, Budiman; McBratney, Alex; de Bruyn, Hank

    2010-05-01

    Soil organic matter (SOM) is composed of a variety of carbon bearing forms which are variably susceptible to degradation, itself a function of soil conditions (moisture, permeability, pH, Eh). Stability and residence time have become key questions relevant to soil carbon storage. Interestingly, organic matter types also differ in terms of their refractory stabilities making thermal analysis potentially an ideal way to resolve and analyse SOM. Elemental analyses of soils are routinely used to provide accurate total carbon determinations for the subsamples in question but cannot yield information about the relative amounts of labile to more stable carbon without involved chemical pre-treatment. Thermogravimetric analyses (TGA) have been commonly used to characterise chemical decomposition and to provide distinctive fingerprints (due to discrete mass changes) for mineral and organic materials. Such discrete changes in mass appear as peaks when registered on a DTGA (differential TGA) plot and correspond with dehydration, denaturing or oxidation events. Soil being a more complex continuum of organic and inorganic substances, many from fermentation reactions and microbial waste, does not have one particular fingerprint. Nonetheless, a number of relevant organic substances have characteristically different but consistent ignition temperatures (Lopez-Capel et. al., 2006; Laird et al., 2008; Xie et. al., 2009) allowing carbon pools to be distinguished thermally. In our studies, oxidative DTGA analyses of soils using a TA 2590 were typified by a bimodal distribution in SOM representing one less stable and one more stable group, a pattern similarly described by Siewert (2004). Current experiments indicate that the relative proportions of these SOM pulses are fairly reproducible but vary depending on soils and sampling depth (i.e. conditions) enabling it as a diagnostic parameter when considering SOM dynamics and humification. In order to compare this property numerically

  8. Driving Factors of Carbon Distribution in Soils as Determined by z*

    NASA Astrophysics Data System (ADS)

    Mnich, M.; Lawrence, C. R.; Harden, J. W.; Treat, C. C.; Schulz, M. S.

    2015-12-01

    Terrestrial soils store approximately three times the amount of carbon(C) stored in the atmosphere. Understanding the mechanisms resulting in soil organic carbon stabilization is necessary for predicting the fate of this carbon and potential feedbacks to climate change. Here, we explore how soil carbon depth gradients are influenced by factors such as age, parent material, mean annual temperature (MAT) and a modeled moisture/leaching index (LI). Specifically, we calculate a quantitative metric reflecting the depth gradient of organic carbon, z*, described by Rosenbloom et al. 2006, which describes the depth attenuation of C turnover by fitting the %C by depth relationship with an exponential decay function. We compare z* across several soil chronosequences (n=33) spanning a broad array of ecosystems and climates. The compiled chronosequence data were collected from previously published studies and ongoing USGS work. Each sequence consisted of at least two soils spanning a developmental age gradient and each soil included depth resolved carbon concentrations, with at least four different depths sampled in vertical profile. When the soil profile data were integrated across all depths, we found only weak relationships between total C in these profiles with various soil forming factors. Comparing depth resolved concentrations provided an opportunity to determine the significance of depth resolved gradients and particularly the importance of deep soil C. We found a significant positive relationship between z* and age, (R2=0.57, p=4.0*10-13), a significant negative relationship between z* and LI (R2=0.02, p=0.02), a significant relationship between (age x LI) and z* (R2=0.02, p=0.02, a positive relationship between z* and MAT (R2=0.1 p=0.01), and no relationship between z* and general parent material type (felsic, mafic, calcareous ; R2=0.04, p=0.01). These findings aid in determining the drivers of soil carbon storage across sites.

  9. Unexpected capacity for organic carbon assimilation by Thermosynechococcus elongatus, a crucial photosynthetic model organism.

    PubMed

    Zilliges, Yvonne; Dau, Holger

    2016-04-01

    Genetic modification of key residues of photosystems is essential to identify functionally crucial processes by spectroscopic and crystallographic investigation; the required protein stability favours use of thermophilic species. The currently unique thermophilic photosynthetic model organism is the cyanobacterial genus Thermosynechococcus. We report the ability of Thermosynechococcus elongatus to assimilate organic carbon, specifically D-fructose. Growth in the presence of a photosynthesis inhibitor opens the door towards crucial amino acid substitutions in photosystems by the rescue of otherwise lethal mutations. Yet depression of batch-culture growth after 7 days implies that additional developments are needed. PMID:26935247

  10. Soil salinity decreases global soil organic carbon stocks.

    PubMed

    Setia, Raj; Gottschalk, Pia; Smith, Pete; Marschner, Petra; Baldock, Jeff; Setia, Deepika; Smith, Jo

    2013-11-01

    Saline soils cover 3.1% (397 million hectare) of the total land area of the world. The stock of soil organic carbon (SOC) reflects the balance between carbon (C) inputs from plants, and losses through decomposition, leaching and erosion. Soil salinity decreases plant productivity and hence C inputs to the soil, but also microbial activity and therefore SOC decomposition rates. Using a modified Rothamsted Carbon model (RothC) with a newly introduced salinity decomposition rate modifier and a plant input modifier we estimate that, historically, world soils that are currently saline have lost an average of 3.47 tSOC ha(-1) since they became saline. With the extent of saline soils predicted to increase in the future, our modelling suggests that world soils may lose 6.8 Pg SOC due to salinity by the year 2100. Our findings suggest that current models overestimate future global SOC stocks and underestimate net CO2 emissions from the soil-plant system by not taking salinity effects into account. From the perspective of enhancing soil C stocks, however, given the lower SOC decomposition rate in saline soils, salt tolerant plants could be used to sequester C in salt-affected areas. PMID:22959898

  11. Black Carbon in Estuarine and Coastal Ocean Dissolved Organic Matter

    NASA Technical Reports Server (NTRS)

    Mannino, Antonio; Harvey, H. Rodger

    2003-01-01

    Black carbon (BC) in ultrafiltered high-molecular-weight DOM (UDOM) was measured in surface waters of Delaware Bay, Chesapeake Bay and the adjacent Atlantic Ocean (USA) to ascertain the importance of riverine and estuarine DOM as a source of BC to the ocean. BC comprised 5-72% of UDOM-C (27+/-l7%) and on average 8.9+/-6.5% of dissolved organic carbon (DOC) with higher values in the turbid region of the Delaware Estuary and lower yields in the river and coastal ocean. The spatial and seasonal distributions of BC along the salinity gradient of Delaware Bay suggest that the higher levels of BC in surface water UDOM originated from localized sources, possibly from atmospheric deposition or released from resuspended sediments. Black carbon comprised 4 to 7% of the DOC in the coastal Atlantic Ocean, revealing that river-estuary systems are important exporters of colloidal BC to the ocean. The annual flux of BC from Delaware Bay UDOM to the Atlantic Ocean was estimated at 2.4x10(exp 10) g BC yr(exp -1). The global river flux of BC through DOM to the ocean could be on the order of 5.5x1O(exp 12)g BC yr (exp -1). These results support the hypothesis that the DOC pool is the intermediate reservoir in which BC ages prior to sedimentary deposition.

  12. Classroom Determination of Trace Organic Substances by Catalytic Methods.

    ERIC Educational Resources Information Center

    Wenck, Helmut; And Others

    1988-01-01

    Describes three trace determinations of organic substances utilizing a spectrophotometer. Provides procedures and absorbance wavelengths for determining acetonitrile, oxalic acid, and oxalic acid in human serum. Explores the role of acetonitrile and oxalic acid as catalysts in their respective reactions. (ML)

  13. REMOVAL OF ORGANIC POLLUTANTS FROM SUBCRITICAL WATER WITH ACTIVATED CARBON

    SciTech Connect

    Steven B. Hawthorne; Arnaud J. Lagadec

    1999-08-01

    The Energy & Environmental Research Center (EERC) has demonstrated that controlling the temperature (and to a lesser extent, the pressure) of water can dramatically change its ability to extract organics and inorganics from matrices ranging from soils and sediments to waste sludges and coal. The dielectric constant of water can be changed from about 80 (a very polar solvent) to <5 (similar to a nonpolar organic solvent) by controlling the temperature (from ambient to about 400 C) and pressure (from about 5 to 350 bar). The EERC has shown that hazardous organic pollutants such as pesticides, PACS (polycyclic aromatic hydrocarbons), and PCBs (polychlorinated biphenyls) can be completely removed from soils, sludges, and sediments at temperatures (250 C) and pressures (<50 atm) that are much milder than typically used for supercritical water processes (temperature >374 C, pressure >221 atm). In addition, the process has been demonstrated to be particularly effective for samples containing very high levels of contaminants (e.g., part per thousand). Current projects include demonstrating the subcritical water remediation process at the pilot scale using an 8-liter system constructed under separate funding during 1997. To date, subcritical water has been shown to be an effective extraction fluid for removing a variety of organic pollutants from soils and sludges contaminated with fossil fuel products and waste products, including PACS from soil (e.g., town gas sites), refining catalysts, and petroleum tank bottom sludges; PCBs from soil and sediments; toxic gasoline components (e.g., benzene) from soil and waste sludge; and phenols from petroleum refinery sludges. The obvious need to clean the wastewater from subcritical water processes led to preliminary experiments with activated carbon placed in line after the extractor. Initial experiments were performed before and after cooling the extractant water (e.g., with water at 200 C and with water cooled to 25 C

  14. Scattered organic matter of carbonate rocks; main forms, evolutionary characteristics and importance in evaluating oil and gas content

    SciTech Connect

    Fu. J.; Jia, R.

    1984-01-01

    It is stated that in relation to the evolution of SOM in carbonate rocks, there are 2 important aspects related to the features of diagenesis of these rocks: 1) displacement of organic matter from the rock because of crystal growth, resulting in a decrease in the total quantity of organic matter in carbonates which is especially significant at early stages of diagenesis; 2) isolation (''protection'') of organic matter by the mineral mass which is the most characteristic for the late stages of diagenesis. The SOM of carbonate rocks can be divided into three types according to the nature of organic matter and the type of protection in diagenesis: 1) absorbed, 2) in crystallization traps, 3) organic inclusions. Protection by the mineral mass means that the processes of SOM metamorphism occurs very slowly, therefore determination of the degree of SOM maturity in the crystallization traps plays an important role in determining the generation potential of the carbonates. A large part of the inclusions is represented by organic matter which has migrated, therefore, study of the inclusion matter is important for studying the primary and secondary migration, as well as for hydrocarbon accumulation in the carbonates.

  15. Fates of eroded soil organic carbon: Mississippi Basin case study

    USGS Publications Warehouse

    Smith, S.V.; Sleezer, R.O.; Renwick, W.H.; Buddemeier, R.W.

    2005-01-01

    We have developed a mass balance analysis of organic carbon (OC) across the five major river subsystems of the Mississippi (MS) Basin (an area of 3.2 ?? 106 km2). This largely agricultural landscape undergoes a bulk soil erosion rate of ???480 t??km -2??yr-1 (???1500 ?? 106 t/yr, across the MS Basin), and a soil organic carbon (SOC) erosion rate of ???7 t??km-2??yr-1 (???22 ?? 106 t/yr). Erosion translocates upland SOC to alluvial deposits, water impoundments, and the ocean. Soil erosion is generally considered to be a net source of CO2 release to the atmosphere in global budgets. However, our results indicate that SOC erosion and relocation of soil apparently can reduce the net SOC oxidation rate of the original upland SOC while promoting net replacement of eroded SOC in upland soils that were eroded. Soil erosion at the MS Basin scale is, therefore, a net CO2 sink rather than a source. ?? 2005 by the Ecological Society of America.

  16. Soil Organic Carbon Mapping by Geostatistics in Europe Scale

    NASA Astrophysics Data System (ADS)

    Aksoy, E.; Panagos, P.; Montanarella, L.

    2013-12-01

    Accuracy in assessing the distribution of soil organic carbon (SOC) is an important issue because SOC is an important soil component that plays key roles in the functions of both natural ecosystems and agricultural systems. The SOC content varies from place to place and it is strongly related with climate variables (temperature and rainfall), terrain features, soil texture, parent material, vegetation, land-use types, and human management (management and degradation) at different spatial scales. Geostatistical techniques allow for the prediction of soil properties using soil information and environmental covariates. In this study, assessment of SOC distribution has been predicted with Regression-Kriging method in Europe scale. In this prediction, combination of the soil samples which were collected from the LUCAS (European Land Use/Cover Area frame statistical Survey) & BioSoil Projects, with local soil data which were collected from six different CZOs in Europe and ten spatial predictors (slope, aspect, elevation, CTI, CORINE land-cover classification, parent material, texture, WRB soil classification, annual average temperature and precipitation) were used. Significant correlation between the covariates and the organic carbon dependent variable was found. Moreover, investigating the contribution of local dataset in watershed scale into regional dataset in European scale was an important challenge.

  17. Effect of biomass adaptation to biodegradation of dissolved organic carbon in water.

    PubMed

    Tihomirova, K; Briedis, A; Rubulis, J; Juhna, T

    2012-04-01

    In the present study the time of adaptation of fixed biomass for biodegradation of natural organic matter was investigated. The experiments were done in columns that are usually used for rapid determination of biodegradable dissolved organic carbon (BDOC). The biomass was adapted to samples with different concentrations of organic substances before measurements by pumping water to be investigated through the columns for several days. The time of adaptation was dependent on the initial concentration of the organic matter in the water sample. The adaptation time increased from 6 to 24 h with increase of concentration of acetate solution from 2 to 10 mg/l, thus adaptation rate decreased simultaneously from 0.28 to 0.11 min(-1). In natural water samples with the initial concentration in the range from 4.61-10.82 mg/l of dissolved organic carbon (DOC) the maximal adaptation time was less than 24 h. During the adaptation period the increase in reproducibility and decrease in the standard deviation was observed. The study showed that adaptation of column to the different concentration of organic matter in water sample is necessary in order to decrease the bias in BDOC measurements when using columns tests. PMID:21892664

  18. Determining Sorption Properties of Pyrogenic Black Carbon for Some Heavy Metals

    NASA Astrophysics Data System (ADS)

    Nicholls, P.; Cadol, D. D.; Galanter, A.

    2014-12-01

    There have been two major fires in the Valles Caldera, located in the Jemez Mountains of Northern New Mexico, within the last three years: the Thompson Ridge fire (June 2013) and the Las Conchas fire (July 2011). During forest fires, contaminants are released from the incomplete combustion of organic matter, from mineral assemblages of the natural soil, and from pre-existing contaminants that have accumulated in biomass and soils. The transport and sequestration of these contaminants is an important factor in determining environmental soil and water quality following fires. Soils containing black carbon (BC) have high sorption capacities for certain contaminants due to its high surface area and cation exchange capacity. The purpose of this project is to quantify the sorption properties of pyrogenic black carbon (PyC), or black carbon formed after the incomplete combustion of organic carbon during forest fires, and soils found in recently burned areas of Northern NM and to determine the environmental impact of soils containing PyC. We used batch equilibrium experiments to determine the sorption properties of BC for selected metals (chromium, lead, and arsenic). Samples tested include naturally occurring soils, concentrated PyC, mixtures of soil and PyC, industrial BC, and a control with low carbon and sorption. Contaminant concentrations were also measured from the soils sampled in the field site. Preliminary results suggest that industrial BC has the highest sorption capacity for heavy metals and the quickest time to equilibrium. As PyC concentrations in the soil increase, sorption capacity is expected to increase. With complete results, the environmental significance of black carbon in the soil, including how PyC affects the transport of solutes in soils, will be evaluated.

  19. Atmospheric Deposition of Organic Carbon in Pennsylvania as Affected by Climatic Factors

    NASA Astrophysics Data System (ADS)

    Iavorivska, L.; Boyer, E. W.; Grimm, J.; Fuentes, J. D.

    2014-12-01

    Organic matter which is usually expressed through measurements of dissolved organic carbon (DOC) is ubiquitous in atmospheric water. It plays an important role in cloud formation processes, and contributes to organic acidity of precipitation. Rain and snow deposited to the landscape is a source of nutrient enrichment to ecosystems and water bodies, and is especially important as an input of carbon in coastal regions. Since DOC is highly chemically reactive and bioavailable it influences rates of primary and secondary productivity in aquatic ecosystems. Despite the significance of DOC to many ecosystem processes, knowledge about its contributions to landscapes in precipitation remains limited. Here, we quantified the removal of DOC from the atmosphere via precipitation over space and time in order to assess the magnitude of wet deposition as a link between terrestrial and aquatic components of the carbon cycle. Further, we consider the predictability of organic matter in precipitation as a function of hydro-chemical and climatic variables. We measured DOC concentration and composition in storm events both sequentially (hourly during events) and seasonally (weekly over the year). Data on the chemical composition of precipitation, along with meteorological back-trajectory analyses help clarify how an interplay between emission sources, atmospheric transport and climatic conditions determine the abundance of rainwater DOC across Pennsylvania.

  20. Dissolved Organic Carbon Mobilisation in a Groundwater System Stressed by Pumping

    NASA Astrophysics Data System (ADS)

    Graham, P. W.; Baker, A.; Andersen, M. S.

    2015-12-01

    The concentration and flux of organic carbon in aquifers is influenced by recharge and abstraction, and surface and subsurface processing. In this study groundwater was abstracted from a shallow fractured rock aquifer and dissolved organic carbon (DOC) was measured in observation bores at different distances from the abstraction bore. Groundwater abstraction at rates exceeding the aquifers yield resulted in increased DOC concentration up to 3,500 percent of initial concentrations. Potential sources of this increased DOC were determined using optical fluorescence and absorbance analysis. Groundwater fluorescent dissolved organic material (FDOM) were found to be a combination of terrestrial-derived humic material and microbial or protein sourced material. Relative molecular weight of FDOM within four metres of the abstraction well increased during the experiment, while the relative molecular weight of FDOM between four and ten metres from the abstraction well decreased. When the aquifer is not being pumped, DOC mobilisation in the aquifer is low. We hypothesise that the physical shear stress on aquifer materials caused by intense abstraction significantly increases the temporary release of DOC from sloughing of biofilms and release of otherwise bound colloidal and sedimentary organic carbon (SOC).

  1. Dissolved Organic Carbon Mobilisation in a Groundwater System Stressed by Pumping

    PubMed Central

    Graham, P. W.; Baker, A.; Andersen, M. S.

    2015-01-01

    The concentration and flux of organic carbon in aquifers is influenced by recharge and abstraction, and surface and subsurface processing. In this study groundwater was abstracted from a shallow fractured rock aquifer and dissolved organic carbon (DOC) was measured in observation bores at different distances from the abstraction bore. Groundwater abstraction at rates exceeding the aquifers yield resulted in increased DOC concentration up to 3,500 percent of initial concentrations. Potential sources of this increased DOC were determined using optical fluorescence and absorbance analysis. Groundwater fluorescent dissolved organic material (FDOM) were found to be a combination of terrestrial-derived humic material and microbial or protein sourced material. Relative molecular weight of FDOM within four metres of the abstraction well increased during the experiment, while the relative molecular weight of FDOM between four and ten metres from the abstraction well decreased. When the aquifer is not being pumped, DOC mobilisation in the aquifer is low. We hypothesise that the physical shear stress on aquifer materials caused by intense abstraction significantly increases the temporary release of DOC from sloughing of biofilms and release of otherwise bound colloidal and sedimentary organic carbon (SOC). PMID:26691238

  2. Dissolved Organic Carbon Mobilisation in a Groundwater System Stressed by Pumping.

    PubMed

    Graham, P W; Baker, A; Andersen, M S

    2015-01-01

    The concentration and flux of organic carbon in aquifers is influenced by recharge and abstraction, and surface and subsurface processing. In this study groundwater was abstracted from a shallow fractured rock aquifer and dissolved organic carbon (DOC) was measured in observation bores at different distances from the abstraction bore. Groundwater abstraction at rates exceeding the aquifers yield resulted in increased DOC concentration up to 3,500 percent of initial concentrations. Potential sources of this increased DOC were determined using optical fluorescence and absorbance analysis. Groundwater fluorescent dissolved organic material (FDOM) were found to be a combination of terrestrial-derived humic material and microbial or protein sourced material. Relative molecular weight of FDOM within four metres of the abstraction well increased during the experiment, while the relative molecular weight of FDOM between four and ten metres from the abstraction well decreased. When the aquifer is not being pumped, DOC mobilisation in the aquifer is low. We hypothesise that the physical shear stress on aquifer materials caused by intense abstraction significantly increases the temporary release of DOC from sloughing of biofilms and release of otherwise bound colloidal and sedimentary organic carbon (SOC). PMID:26691238

  3. Microbial and Mineral Controls on Soil Organic Carbon Decomposition: Testing the MEND Model with Data from Lab Incubations

    NASA Astrophysics Data System (ADS)

    Wang, G.; Jagadamma, S.; Steinweg, J. M.; Mayes, M. A.; Post, W. M.

    2012-12-01

    Microbes (including enzymes) and physical-chemical protection play important roles in controlling soil organic carbon (SOC) decomposition. The Microbial-ENzyme-mediated Decomposition (MEND) model was used to examine the dynamics of physically fractionated SOC pools in lab incubation experiments. The carbon pools in MEND consist of particulate, mineral-associated, dissolved organic carbon (POC, MOC, and DOC, respectively), microbial biomass, and associated exoenzymes. The following component carbon fluxes are described in MEND: POC and MOC decomposition, DOC uptake by microbes, adsorption and desorption of DOC, microbial growth and maintenance respiration, microbial mortality, and enzyme production and turnover. The kinetic parameters pertaining to these processes were determined based on the measured respiration processes and the a priori ranges/distributions of parameters. We attempted to demonstrate different dynamics of POC and MOC pools regulated by microbial-enzyme activities under different physical-chemical circumstances. Carbon pools and fluxes in the microbial-enzyme-mediated decomposition model

  4. Organic carbon pools in Austrian permanent grassland soils

    NASA Astrophysics Data System (ADS)

    Foldal, Cecilie B.; Bohner, Andreas; Jandl, Robert

    2015-04-01

    Grasslands are known to store large amounts of carbon (C) and land use and farming management practices do have an impact on the quantity of soil organic carbon (SOC) as well as the biomass production. In the period from 1995 to 2010 the total area for agriculture and forest production in Austria declined and the most severe changes took place in grassland areas where more than 25% of the land used for extensive or intensive grass production was lost due to land use change, abandonment or sealing. In this study, we investigated the organic carbon (OC) stock at three different locations representative for Austrian mountainous grassland regions. At each location we compared the above- and belowground (down to 50 cm depth) C stocks at two adjacent but differently managed sites in order to see how management intensity affects the OC pools in permanent grassland soils. Mean OC stocks ranged from 8.2 to 15.7 kg per m² whereby approximately 95% was allocated belowground. In general, we found a significant positive correlation between the SOC content and biomass production at all three locations. Mean root biomass content ranged from 0.205 to 1.950 kg per m². 78.2 to 93.2% of root biomass was concentrated in the top 10 cm of the soil. Management had a significant influence on the SOC content as well as on above- and belowground biomass production. We conclude that permanent grassland soils represent a large sink for OC. Root biomass and SOC content respond to management intensity.

  5. Estimating the Age Distribution of Oceanic Dissolved Organic Carbon

    NASA Astrophysics Data System (ADS)

    Follett, C. L.; Forney, D. C.; Repeta, D.; Rothman, D.

    2010-12-01

    Dissolved organic carbon (DOC) is a large, ubiquitous component of open ocean water at all depths and impacts atmospheric carbon dioxide levels at both short and long timescales. It is currently believed that oceanic DOC contains a multi-thousand-year-old refractory deep-water component which is mixed with a young labile component in surface waters. Unfortunately, the only evidence for this comes from a few isolated depth profiles of both DOC concentration and bulk radiocarbon. Although the profile data is consistent with a two-component mixing model, directly separating the two components has proven to be a challenge. We explore the validity of the two component mixing model by directly estimating the age distribution of oceanic DOC. The two-component model suggests that the age distribution is composed of two distinct peaks. In order to obtain an estimate of the age distribution we first record changes in both concentration and percent radiocarbon as a sample is oxidized under ultra-violet radiation [1]. We formulate a mathematical model relating the age distribution to these changes, assuming that they result from components of different radiocarbon age and UV-reactivity. This allows us to numerically invert the data and estimate the age distribution. We apply our procedure to DOC samples collected from three distinct depths (50, 500, and 2000 meters) in the north-central Pacific Ocean. [1] S.R. Beaupre, E.R.M. Druffel, and S. Griffin. A low-blank photochemical extraction system for concentration and isotopic analyses of marine dissolved organic carbon. Limnol. Oceanogr. Methods, 5:174-184, 2007.

  6. Analytical methods for the determination of carbon tetrachloride in soils.

    SciTech Connect

    Alvarado, J. S.; Spokas, K.; Taylor, J.

    1999-06-01

    Improved methods for the determination of carbon tetrachloride are described. These methods incorporate purge-and-trap concentration of heated dry samples, an improved methanol extraction procedure, and headspace sampling. The methods minimize sample pretreatment, accomplish solvent substitution, and save time. The methanol extraction and headspace sampling procedures improved the method detection limits and yielded better sensitivity, good recoveries, and good performance. Optimization parameters are shown. Results obtained with these techniques are compared for soil samples from contaminated sites.

  7. EPIC Simulations of Crop Yields and Soil Organic Carbon in Iowa

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Depending on management, soil organic carbon is source or sink of atmospheric carbon dioxide. The Environmental Policy Integrated Climate (EPIC) model is a useful tool for predicting impacts of soil management on crop yields and soil organic carbon. We used EPIC-Century to simulate changes in soil o...

  8. Relationships between pesticides and organic carbon fractions in sediments of the Danshui River estuary and adjacent coastal areas of Taiwan.

    PubMed

    Hung, Chin-Chang; Gong, Gwo-Ching; Chen, Hung-Yu; Hsieh, Hwey-Lian; Santschi, Peter H; Wade, Terry L; Sericano, Jose L

    2007-07-01

    In order to understand the fate of pesticides in marine environments, concentrations of pesticides and different carbonaceous fractions were determined for surface sediments in the Danshui River and nearby coastal areas of Taiwan. The major compounds detected were tetrachlorobenzene, HCHs, chlordane, aldrin, DDDs, DDEs and DDTs. Total concentrations of pesticides in the sediments ranged from not detectable to 23 ng g(-1), with the maximum value detected near the discharge point of the marine outfall from the Pali sewage treatment plant. These results confirm that pesticides persist in estuarine and nearby coastal environments of the Danshui River well after their ban. Concentrations of total pesticides significantly correlate with concentrations of total organic carbon and black carbon in these sediments, suggesting that total organic carbon and black carbon regulate the distribution of trace organic pollutants in fluvial and coastal marine sediments. PMID:17395347

  9. Isotope-based Fluvial Organic Carbon (ISOFLOC) Model: Model formulation, sensitivity, and evaluation

    NASA Astrophysics Data System (ADS)

    Ford, William I.; Fox, James F.

    2015-06-01

    Watershed-scale carbon budgets remain poorly understood, in part due to inadequate simulation tools to assess in-stream carbon fate and transport. A new numerical model termed ISOtope-based FLuvial Organic Carbon (ISOFLOC) is formulated to simulate the fluvial organic carbon budget in watersheds where hydrologic, sediment transport, and biogeochemical processes are coupled to control benthic and transported carbon composition and flux. One ISOFLOC innovation is the formulation of new stable carbon isotope model subroutines that include isotope fractionation processes in order to estimate carbon isotope source, fate, and transport. A second innovation is the coupling of transfers between carbon pools, including algal particulate organic carbon, fine particulate and dissolved organic carbon, and particulate and dissolved inorganic carbon, to simulate the carbon cycle in a comprehensive manner beyond that of existing watershed water quality models. ISOFLOC was tested and verified in a low-gradient, agriculturally impacted stream. Results of a global sensitivity analysis suggested the isotope response variable had unique sensitivity to the coupled interaction between fluvial shear resistance of algal biomass and the concentration of dissolved inorganic carbon. Model calibration and validation suggested good agreement at event, seasonal, and annual timescales. Multiobjective uncertainty analysis suggested inclusion of the carbon stable isotope routine reduced uncertainty by 80% for algal particulate organic carbon flux estimates.

  10. Organic carbon dynamics in the Mediterranean Sea: An integrated study

    NASA Astrophysics Data System (ADS)

    Santinelli, Chiara; SempéRé, Richard; van Wambeke, France; Charriere, Bruno; Seritti, Alfredo

    2012-12-01

    Total (TOC) and dissolved (DOC) organic carbon vertical profiles were analyzed from 11 stations located in various regions of the Mediterranean Sea, together with the distribution of other physical, chemical and biological parameters. TOC showed the highest concentrations (68-83 μM) above the pycnocline, followed by a marked decrease to values of 45-48 μM at 100-200 m. Below 200 m, values of 40-45 μM were observed. The excess TOC and DOC occurring at each station was calculated by subtracting 48 μM from the observed concentrations. The stock of the excess TOC and DOC increased eastward; while surface DOC mineralization rates decreased from 1.5 μM d-1 to 0.26 μM d-1 eastward. The integrated average of the biological parameters in the above-pycnocline layer showed a bacterial production versus particulate primary production (BP/PPP) ratio ranging from 22% in the Ionian Sea (MIO station) to 31% in the Ligurian Sea (Dyfamed station), while bacterial carbon demand versus PPP was higher than 100%, considering a bacterial growth efficiency of both 15% and 30%. The data here reported indicate various scenarios of carbon dynamics. At the stations west of the Sardinian Channel, the microbial loop was very active, and a high flux of carbon to the microbial loop (large bacterial and protist abundance) may be hypothesized, which would result in a low DOC concentration. At the stations east of the Sardinian Channel, no significant longitudinal variation was found in DOC and BP. DOC accumulated at these stations, possibly due to bacteria P-limitation, to DOC chemical composition and/or to the occurrence of different prokaryotic populations with a different ability to consume the available DOC.

  11. Inputs of organic carbon from Ria de Aveiro coastal lagoon to the Atlantic Ocean

    NASA Astrophysics Data System (ADS)

    Lopes, C. B.; Lillebø, A. I.; Pato, P.; Dias, J. M.; Rodrigues, S. M.; Pereira, E.; Duarte, A. C.

    2008-09-01

    Land/ocean boundaries constitute complex systems with active physical and biogeochemical processes that affect the global carbon cycle. An example of such a system is the mesotidal lagoon named Ria de Aveiro (Portugal, 40°38'N, 08°45'W), which is connected to the Atlantic Ocean by a single channel, 350 m wide. The objective of this study was to estimate the seasonal and inter-tidal variability of organic carbon fluxes between the coastal lagoon and the Ocean, and to assess the contribution of the organic carbon fractions (i.e. dissolved organic carbon (DOC) and particulate organic carbon (POC)) to the export of organic carbon to the Ria de Aveiro plume zone. The organic carbon fractions fluxes were estimated as the product of the appropriate fractional organic carbon concentrations and the water fluxes calculated by a two-dimensional vertically integrated hydrodynamic model (2DH). Results showed that the higher exchanges of DOC and POC fractions at the system cross-section occurred during spring tides but only resulted in a net export of organic carbon in winter, totalling 85 t per tidal cycle. Derived from the winter and summer campaigns, the annual carbon mass balance estimated corresponded to a net export of organic carbon (7957 = 6585 t yr -1 POC + 1372 t yr -1 DOC). On the basis of the spring tidal drainage area, it corresponds to an annual flux of 79 g m -2 of POC and 17 g m -2 of DOC out of the estuary.

  12. Spring Hydrology Determines Summer Net Carbon Uptake in Northern Ecosystems

    NASA Technical Reports Server (NTRS)

    Yi, Yonghong; Kimball, John; Reichle, Rolf H.

    2014-01-01

    Increased photosynthetic activity and enhanced seasonal CO2 exchange of northern ecosystems have been observed from a variety of sources including satellite vegetation indices (such as the Normalized Difference Vegetation Index; NDVI) and atmospheric CO2 measurements. Most of these changes have been attributed to strong warming trends in the northern high latitudes (greater than or equal to 50N). Here we analyze the interannual variation of summer net carbon uptake derived from atmospheric CO2 measurements and satellite NDVI in relation to surface meteorology from regional observational records. We find that increases in spring precipitation and snow pack promote summer net carbon uptake of northern ecosystems independent of air temperature effects. However, satellite NDVI measurements still show an overall benefit of summer photosynthetic activity from regional warming and limited impact of spring precipitation. This discrepancy is attributed to a similar response of photosynthesis and respiration to warming and thus reduced sensitivity of net ecosystem carbon uptake to temperature. Further analysis of boreal tower eddy covariance CO2 flux measurements indicates that summer net carbon uptake is positively correlated with early growing-season surface soil moisture, which is also strongly affected by spring precipitation and snow pack based on analysis of satellite soil moisture retrievals. This is attributed to strong regulation of spring hydrology on soil respiration in relatively wet boreal and arctic ecosystems. These results document the important role of spring hydrology in determining summer net carbon uptake and contrast with prevailing assumptions of dominant cold temperature limitations to high-latitude ecosystems. Our results indicate potentially stronger coupling of boreal/arctic water and carbon cycles with continued regional warming trends.

  13. [Qualitative Determination of Organic Vapour Using Violet and Visible Spectrum].

    PubMed

    Jiang, Bo; Hu, Wen-zhong; Liu, Chang-jian; Zheng, Wei; Qi, Xiao-hui; Jiang, Ai-li; Wang, Yan-ying

    2015-12-01

    Vapours of organic matters were determined qualitatively employed with ultraviolet-visible absorption spectroscopy. Vapours of organic matters were detected using ultraviolet-visible spectrophotometer employing polyethylene film as medium, the ultraviolet and visible absorption spectra of vegetable oil vapours of soybean oil, sunflower seed oil, peanut oil, rapeseed oil, sesame oil, cotton seed oil, tung tree seed oil, and organic compound vapours of acetone, ethyl acetate, 95% ethanol, glacial acetic acid were obtained. Experimental results showed that spectra of the vegetable oil vapour and the organic compound vapour could be obtained commendably, since ultra violet and visible spectrum of polyethylene film could be deducted by spectrograph zero setting. Different kinds of vegetable oils could been distinguished commendably in the spectra since the λ(max), λ(min), number of absorption peak, position, inflection point in the ultra violet and visible spectra obtained from the vapours of the vegetable oils were all inconsistent, and the vapours of organic compounds were also determined perfectly. The method had a good reproducibility, the ultraviolet and visible absorption spectra of the vapours of sunflower seed oil in 10 times determination were absolutely the same. The experimental result indicated that polyethylene film as a kind of medium could be used for qualitative analysis of ultraviolet and visible absorption spectroscopy. The method for determination of the vapours of the vegetable oils and organic compounds had the peculiarities of fast speed analysis, well reproducibility, accuracy and reliability and low cost, and so on. Ultraviolet and visible absorption spectrum of organic vapour could provide feature information of material vapour and structural information of organic compound, and provide a novel test method for identifying vapour of compound and organic matter. PMID:26964229

  14. Liquid-phase adsorption of organic compounds by granular activated carbon and activated carbon fibers

    SciTech Connect

    Lin, S.H.; Hsu, F.M.

    1995-06-01

    Liquid-phase adsorption of organic compounds by granular activated carbon (GAC) and activated carbon fibers (ACFs) is investigated. Acetone, isopropyl alcohol (IPA), phenol, and tetrahydrofuran (THF) were employed as the model compounds for the present study. It is observed from the experimental results that adsorption of organic compounds by GAC and ACF is influenced by the BET (Brunauer-Emmett-Teller) surface area of adsorbent and the molecular weight, polarity, and solubility of the adsorbate. The adsorption characteristics of GAC and ACFs were found to differ rather significantly. In terms of the adsorption capacity of organic compounds, the time to reach equilibrium adsorption, and the time for complete desorption, ACFs have been observed to be considerably better than GAC. For the organic compounds tested here, the GAC adsorptions were shown to be represented well by the Langmuir isotherm while the ACF adsorption could be adequately described by the Langmuir or the Freundlich isotherm. Column adsorption tests indicated that the exhausted ACFs can be effectively regenerated by static in situ thermal desorption at 150 C, but the same regeneration conditions do not do as well for the exhausted GAC.

  15. Organic and Elemental Carbon Filter Sets: Preparation Method and Interlaboratory Results

    PubMed Central

    Chai, Ming; Birch, M. Eileen; Deye, Greg

    2012-01-01

    Carbonaceous aerosols play an important role in climate, visibility, air quality, and human health effects, and they have been routinely monitored in workplace and environmental settings. Different thermal analysis methods have been applied to determine the carbon content of carbonaceous aerosols. Good agreement between results for total carbon (TC) generally has been found, but the organic and elemental carbon (OC and EC) fractions determined by different methods often disagree. Measurement uncertainty is mainly due to pyrolysis and charring of OC sample components. Lack of reference materials has impeded progress on method standardization and understanding method biases. A relatively simple method for generating matched filter sets having known OC–EC contents is reported. After generation and analysis of each set to confirm agreement between filters, the filter sets were distributed to six laboratories for an interlaboratory comparison. Analytical results indicate a uniform carbon distribution for the filter sets and good agreement between the participating laboratories. Relative standard deviations (RSDs) for mean TC (OC + EC), OC, and EC results for seven laboratories were <10, 11, and 12% (respectively). Except for one EC result (RSD = 16%), RSDs reported by individual laboratories for TC, OC, and EC were <12%. The method of filter generation is generally applicable and reproducible. Depending on the application, different filter loadings and types of OC materials can be employed. Matched filter sets prepared by the described approach can be used for determining the accuracy of OC–EC methods and thereby contribute to method standardization. PMID:22459320

  16. Soil organic carbon redistribution by water erosion--the role of CO2 emissions for the carbon budget.

    PubMed

    Wang, Xiang; Cammeraat, Erik L H; Romeijn, Paul; Kalbitz, Karsten

    2014-01-01

    A better process understanding of how water erosion influences the redistribution of