Total organic carbon, an important tool in a holistic approach to hydrocarbon source fingerprinting

International Nuclear Information System (INIS)

Boehm, P.D.; Burns, W.A.; Page, D.S.; Bence, A.E.; Mankiewicz, P.J.; Brown, J.S.; Douglas, G.S.

2002-01-01

Total organic carbon (TOC) was used to verify the consistency of source allocation results for the natural petrogenic hydrocarbon background of the northern Gulf of Alaska and Prince William Sound where the Exxon Valdez oil spill occurred in 1998. The samples used in the study were either pre-spill sediments or from the seafloor outside the spill path. It is assumed that the natural petrogenic hydrocarbon background in the area comes from either seep oil residues and shale erosion including erosion from petroleum source rock shales, or from coals including those of the Bering River coalfields. The objective of this study was to use the TOC calculations to discriminate between the two very different sources. TOC can constrain the contributions of specific sources and rule out incorrect source allocations, particularly when inputs are dominated by fossil organic carbon. The benthic sediments used in this study showed excellent agreement between measured TOC and calculated TOC from hydrocarbon fingerprint matches of polycyclic aromatic hydrocarbons (PAH) and chemical biomarkers. TOC and fingerprint matches confirmed that TOC sources were properly identified. The matches quantify the hydrocarbon contributions of different sources to the benthic sediments and the degree of hydrocarbon winnowing by waves and currents. It was concluded that the natural petrogenic hydrocarbon background in the sediments in the area comes from eroding Tertiary shales and oil seeps along the northern Gulf of Alaska coast. Thermally mature area coals are excluded from being important contributors to the background at Prince William Sound because of their high TOC content. 26 refs., 4 figs

Total organic carbon, an important tool in a holistic approach to hydrocarbon source fingerprinting

Energy Technology Data Exchange (ETDEWEB)

Boehm, P.D. [Battelle, Waltham, MA (United States); Burns, W.A. [W.A. Burns Consulting Services, Houston, TX (United States); Page, D.S. [Bowdoin College, Brunswick, ME (United States); Bence, A.E.; Mankiewicz, P.J. [ExxonMobil Upstream Research Co., Houston, TX (United States); Brown, J.S.; Douglas, G.S. [Battelle, Duxbury, MA (United States)

2002-07-01

Total organic carbon (TOC) was used to verify the consistency of source allocation results for the natural petrogenic hydrocarbon background of the northern Gulf of Alaska and Prince William Sound where the Exxon Valdez oil spill occurred in 1998. The samples used in the study were either pre-spill sediments or from the seafloor outside the spill path. It is assumed that the natural petrogenic hydrocarbon background in the area comes from either seep oil residues and shale erosion including erosion from petroleum source rock shales, or from coals including those of the Bering River coalfields. The objective of this study was to use the TOC calculations to discriminate between the two very different sources. TOC can constrain the contributions of specific sources and rule out incorrect source allocations, particularly when inputs are dominated by fossil organic carbon. The benthic sediments used in this study showed excellent agreement between measured TOC and calculated TOC from hydrocarbon fingerprint matches of polycyclic aromatic hydrocarbons (PAH) and chemical biomarkers. TOC and fingerprint matches confirmed that TOC sources were properly identified. The matches quantify the hydrocarbon contributions of different sources to the benthic sediments and the degree of hydrocarbon winnowing by waves and currents. It was concluded that the natural petrogenic hydrocarbon background in the sediments in the area comes from eroding Tertiary shales and oil seeps along the northern Gulf of Alaska coast. Thermally mature area coals are excluded from being important contributors to the background at Prince William Sound because of their high TOC content. 26 refs., 4 figs.

Tracing the sources of organic carbon in freshwater systems

Science.gov (United States)

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.

Long-term trends in California mobile source emissions and ambient concentrations of black carbon and organic aerosol.

Science.gov (United States)

McDonald, Brian C; Goldstein, Allen H; Harley, Robert A

2015-04-21

A fuel-based approach is used to assess long-term trends (1970-2010) in mobile source emissions of black carbon (BC) and organic aerosol (OA, including both primary emissions and secondary formation). The main focus of this analysis is the Los Angeles Basin, where a long record of measurements is available to infer trends in ambient concentrations of BC and organic carbon (OC), with OC used here as a proxy for OA. Mobile source emissions and ambient concentrations have decreased similarly, reflecting the importance of on- and off-road engines as sources of BC and OA in urban areas. In 1970, the on-road sector accounted for ∼90% of total mobile source emissions of BC and OA (primary + secondary). Over time, as on-road engine emissions have been controlled, the relative importance of off-road sources has grown. By 2010, off-road engines were estimated to account for 37 ± 20% and 45 ± 16% of total mobile source contributions to BC and OA, respectively, in the Los Angeles area. This study highlights both the success of efforts to control on-road emission sources, and the importance of considering off-road engine and other VOC source contributions when assessing long-term emission and ambient air quality trends.

Stable carbon isotope ratios: implications for the source of sediment carbon and for phytoplankton carbon assimilation in Lake Memphremagog, Quebec

International Nuclear Information System (INIS)

LaZerte, B.D.

1983-01-01

The stable carbon isotope (SCI) ratio of the sediment of Lake Memphremagog, Quebec is compared with that ot terrestrial sources and the phytoplankton to determine the relative proportion of allochthonous carbon incorporated into the sediments. Approximately 40-50% of the organic carbon in the main basins' pelagic sediment was terrestrial in origin, whereas up to 100% was terrestrial in littoral areas. The SCI method of determining the organic carbon source of sediments appears more reliable than the C/N method. A comparison of the SCI fractionation of the phytoplankton with laboratory cultures under different degrees of carbon limitation indicates that the phytoplankton of Lake Memphremagog are not carbon limited and fix carbon primarily by the C 3 pathway

Isotopic evidence for the influence of typhoons and submarine canyons on the sourcing and transport behavior of biospheric organic carbon to the deep sea

Science.gov (United States)

Zheng, Li-Wei; Ding, Xiaodong; Liu, James T.; Li, Dawei; Lee, Tsung-Yu; Zheng, Xufeng; Zheng, Zhenzhen; Xu, Min Nina; Dai, Minhan; Kao, Shuh-Ji

2017-05-01

Export of biospheric organic carbon from land masses to the ocean plays an important role in regulating the global carbon cycle. High-relief islands in the western Pacific are hotspots for such land-to-ocean carbon transport due to frequent floods and active tectonics. Submarine canyon systems serve as a major conduit to convey terrestrial organics into the deep sea, particularly during episodic floods, though the nature of ephemeral sediment transportation through such canyons remains unclear. In this study, we deployed a sediment trap in southwestern Taiwan's Gaoping submarine canyon during summer 2008, during which Typhoon Kalmaegi impacted the study area. We investigated sources of particulate organic carbon and quantified the content of fossil organic carbon (OCf) and biospheric non-fossil carbon (OCnf) during typhoon and non-typhoon periods, based on relations between total organic carbon (TOC), isotopic composition (δ13 C, 14C), and nitrogen to carbon ratios (N/C) of newly and previously reported source materials. During typhoons, flooding connected terrestrial rivers to the submarine canyon. Fresh plant debris was not found in the trap except in the hyperpycnal layer, suggesting that only hyperpycnal flow is capable of entraining plant debris, while segregation had occurred during non-hyperpycnal periods. The OCnf components in typhoon flood and trapped samples were likely sourced from aged organics buried in ancient landslides. During non-typhoon periods, the canyon is more connected to the shelf, where waves and tides cause reworking, thus allowing abiotic and biotic processes to generate isotopically uniform and similarly aged OCnf for transport into the canyon. Therefore, extreme events coupled with the submarine canyon system created an efficient method for deep-sea burial of freshly produced organic-rich material. Our results shed light on the ephemeral transport of organics within a submarine canyon system on an active tectonic margin.

Organic tracer-based source analysis of PM2.5 organic and elemental carbon: A case study at Dongguan in the Pearl River Delta, China

Science.gov (United States)

Wang, Qiong Qiong; Huang, X. H. Hilda; Zhang, Ting; Zhang, Qingyan; Feng, Yongming; Yuan, Zibing; Wu, Dui; Lau, Alexis K. H.; Yu, Jian Zhen

2015-10-01

Organic carbon (OC) and elemental carbon (EC) are major constituents of PM2.5 and their source apportionment remains a challenging task due to the great diversity of their sources and lack of source-specific tracer data. In this work, sources of OC and EC are investigated using positive matrix factorization (PMF) analysis of PM2.5 chemical composition data, including major ions, OC, EC, elements, and organic molecular source markers, for a set of 156 filter samples collected over three years from 2010 to 2012 at Dongguan in the Pearl River Delta, China. The key organic tracers include levoglucosan, mannosan, hopanes, C27-C33n-alkanes, and polycyclic aromatic hydrocarbons (PAHs). Using these species as input for the PMF model, nine factors were resolved. Among them, biomass burning and coal combustion were significant sources contributing 15-17% of OC and 24-30% and 34-35% of EC, respectively. Industrial emissions and ship emissions, identified through their characteristic metal signatures, contributed 16-24% and 7-8% of OC and 8-11% and 16-17% of EC, respectively. Vehicle exhaust was a less significant source, accounting for 3-4% of OC and 5-8% of EC. Secondary OC, taken to be the sum of OC present in secondary sulfate and nitrate formation source factors, made up 27-36% of OC. Plastic burning, identified through 1,3,5-triphenylbenzene as a tracer, was a less important source for OC(≤4%) and EC (5-10%), but a significant source for PAHs at this site. The utility of organic source tracers was demonstrated by comparing PMF runs with different combinations of organic tracers removed from the input species list. Levoglucosan and mannosan were important additions to distinguish biomass burning from coal combustion by reducing collinearity among source profiles. Inclusion of hopanes and 1,3,5-triphenylbenzene was found to be necessary in resolving the less significant sources vehicle exhaust and plastic burning. Inclusion of C27-C33n-alkanes and PAHs can influence the

Temporal variability in terrestrially-derived sources of particulate organic carbon in the lower Mississippi River and its upper tributaries

Science.gov (United States)

Bianchi, Thomas S.; Wysocki, Laura A.; Stewart, Mike; Filley, Timothy R.; McKee, Brent A.

2007-09-01

In this study, we examined the temporal changes of terrestrially-derived particulate organic carbon (POC) in the lower Mississippi River (MR) and in a very limited account, the upper tributaries (Upper MR, Ohio River, and Missouri River). We used for the first time a combination of lignin-phenols, bulk stable carbon isotopes, and compound-specific isotope analyses (CSIA) to examine POC in the lower MR and upper tributaries. A lack of correlation between POC and lignin phenol abundances ( Λ8) was likely due to dilution effects from autochthonous production in the river, which has been shown to be considerably higher than previously expected. The range of δ 13C values for p-hydroxycinnamic and ferulic acids in POC in the lower river do support that POM in the lower river does have a significant component of C 4 in addition to C 3 source materials. A strong correlation between δ 13C values of p-hydroxycinnamic, ferulic, and vanillyl phenols suggests a consistent input of C 3 and C 4 carbon to POC lignin while a lack of correlation between these same phenols and POC bulk δ 13C further indicates the considerable role of autochthonous carbon in the lower MR POC budget. Our estimates indicate an annual flux of POC of 9.3 × 10 8 kg y -1 to the Gulf of Mexico. Total lignin fluxes, based on Λ8 values of POC, were estimated to be 1.2 × 10 5 kg y -1. If we include the total dissolved organic carbon (DOC) flux (3.1 × 10 9 kg y -1) reported by [Bianchi T. S., Filley T., Dria K. and Hatcher, P. (2004) Temporal variability in sources of dissolved organic carbon in the lower Mississippi River. Geochim. Cosmochim. Acta68, 959-967.], we get a total organic carbon flux of 4.0 × 10 9 kg y -1. This represents 0.82% of the annual total organic carbon supplied to the oceans by rivers (4.9 × 10 11 kg).

Methods of analysis for complex organic aerosol mixtures from urban emission sources of particulate carbon

International Nuclear Information System (INIS)

Mazurek, M.A.; Hildemann, L.M.; Simoneit, B.R.T.

1990-10-01

Organic aerosols comprise approximately 30% by mass of the total fine particulate matter present in urban atmospheres. The chemical composition of such aerosols is complex and reflects input from multiple sources of primary emissions to the atmosphere, as well as from secondary production of carbonaceous aerosol species via photochemical reactions. To identify discrete sources of fine carbonaceous particles in urban atmospheres, analytical methods must reconcile both bulk chemical and molecular properties of the total carbonaceous aerosol fraction. This paper presents an overview of the analytical protocol developed and used in a study of the major sources of fine carbon particles emitted to an urban atmosphere. 23 refs., 1 fig., 2 tabs

Organic carbon input in shallow groundwater at Aspo, southeastern Sweden

International Nuclear Information System (INIS)

Wallin, B.

1993-01-01

The variation in carbon and oxygen isotopes in calcite fissure fillings and dissolved carbonate from shallow groundwaters has been examined at Aspo, southeastern Sweden. The shallow water lens is refilled by meteoric water and is considered as an open system. The σ 13 C-signatures of the dissolved carbonate fall within a narrow range of -15.8 to -17.4 per-thousand, indicative of organic an organic carbon source. The low σ 13 C-values suggest that input of soil-CO 2 is the dominating carbon source for the system. σ 13 C and σ 18 O-values in the calcite fissure fillings show a wide range in values with a possible two end-member mixing of early post glacial atmospheric CO 2 dominated system to a present day soil-CO 2 dominating carbon source

Mangrove litter production and organic carbon pools in the ...

African Journals Online (AJOL)

Mngazana Estuary is an important source of mangrove litter and POC for the adjacent marine environment, possibly sustaining nearshore food webs. Keywords: Dissolved organic carbon, harvesting, litter production, mangroves, particulate organic carbon, Rhizophora mucronata, South Africa African Journal of Aquatic ...

Source contributions to atmospheric fine carbon particle concentrations

Science.gov (United States)

Andrew Gray, H.; Cass, Glen R.

A Lagrangian particle-in-cell air quality model has been developed that facilitates the study of source contributions to atmospheric fine elemental carbon and fine primary total carbon particle concentrations. Model performance was tested using spatially and temporally resolved emissions and air quality data gathered for this purpose in the Los Angeles area for the year 1982. It was shown that black elemental carbon (EC) particle concentrations in that city were dominated by emissions from diesel engines including both on-highway and off-highway applications. Fine primary total carbon particle concentrations (TC=EC+organic carbon) resulted from the accumulation of small increments from a great variety of emission source types including both gasoline and diesel powered highway vehicles, stationary source fuel oil and gas combustion, industrial processes, paved road dust, fireplaces, cigarettes and food cooking (e.g. charbroilers). Strategies for black elemental carbon particle concentration control will of necessity need to focus on diesel engines, while controls directed at total carbon particle concentrations will have to be diversified over a great many source types.

Fossil and non-fossil sources of organic carbon (OC and elemental carbon (EC in Göteborg, Sweden

Directory of Open Access Journals (Sweden)

S. Szidat

2009-03-01

Full Text Available Particulate matter was collected at an urban site in Göteborg (Sweden in February/March 2005 and in June/July 2006. Additional samples were collected at a rural site for the winter period. Total carbon (TC concentrations were 2.1–3.6 μg m⁻³, 1.8–1.9 μg m⁻³, and 2.2–3.0 μg m⁻³ for urban/winter, rural/winter, and urban/summer conditions, respectively. Elemental carbon (EC, organic carbon (OC, water-insoluble OC (WINSOC, and water-soluble OC (WSOC were analyzed for ¹⁴C in order to distinguish fossil from non-fossil emissions. As wood burning is the single major source of non-fossil EC, its contribution can be quantified directly. For non-fossil OC, the wood-burning fraction was determined independently by levoglucosan and ¹⁴C analysis and combined using Latin-hypercube sampling (LHS. For the winter period, the relative contribution of EC from wood burning to the total EC was >3 times higher at the rural site compared to the urban site, whereas the absolute concentrations of EC from wood burning were elevated only moderately at the rural compared to the urban site. Thus, the urban site is substantially more influenced by fossil EC emissions. For summer, biogenic emissions dominated OC concentrations most likely due to secondary organic aerosol (SOA formation. During both seasons, a more pronounced fossil signal was observed for Göteborg than has previously been reported for Zurich, Switzerland. Analysis of air mass origin using back trajectories suggests that the fossil impact was larger when local sources dominated, whereas long-range transport caused an enhanced non-fossil signal. In comparison to other European locations, concentrations of levoglucosan and other monosaccharide anhydrides were low for the urban and the rural site in the area of Göteborg during winter.

Carbon isotope ratios of organic matter in Bering Sea settling particles. Extremely high remineralization of organic carbon derived from diatoms

International Nuclear Information System (INIS)

Yasuda, Saki; Akagi, Tasuku; Naraoka, Hiroshi; Kitajima, Fumio; Takahashi, Kozo

2016-01-01

The carbon isotope ratios of organic carbon in settling particles collected in the highly-diatom-productive Bering Sea were determined. Wet decomposition was employed to oxidize relatively fresh organic matter. The amount of unoxidised organic carbon in the residue following wet decomposition was negligible. The δ 13 C of organic carbon in the settling particles showed a clear relationship against SiO 2 /CaCO 3 ratio of settling particles: approximately -26‰ and -19‰ at lower and higher SiO 2 /CaCO 3 ratios, respectively. The δ 13 C values were largely interpreted in terms of mixing of two major plankton sources. Both δ 13 C and compositional data can be explained consistently only by assuming that more than 98% of diatomaceous organic matter decays and that organic matter derived from carbonate-shelled plankton may remain much less remineralized. A greater amount of diatom-derived organic matter is discovered to be trapped with the increase of SiO 2 /CaCO 3 ratio of the settling particles. The ratio of organic carbon to inorganic carbon, known as the rain ratio, therefore, tends to increase proportionally with the SiO 2 /CaCO 3 ratio under an extremely diatom-productive condition. (author)

Inferring absorbing organic carbon content from AERONET data

Science.gov (United States)

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 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 mg m-2 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 mg m-2 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 the global Oslo CTM for several sites. Model values are higher in biomass burning regions than AERONET-based retrievals, while the opposite is true in urban areas in India and China.

An Ocean Basin of Dirt? Using Molecular Biomarkers and Radiocarbon to Identify Organic Carbon Sources and their Preservation in the Arctic Ocean

Science.gov (United States)

Harvey, H.; Belicka, L. L.

2005-12-01

In the modern Arctic Ocean, primary production in waters over the broad continental shelves and under ice contributes an estimated 250 Mt/yr of POC to Arctic waters. The delivery of terrestrial material from large rivers, ice transport and through coastal erosion adds at least an additional 12 Mt/yr of POC. Although the marine organic carbon signal in Arctic Ocean exceeds that of terrestrial carbon by an order or magnitude or more, recent evidence suggests that this balance is not maintained and significant fractions of terrestrial carbon is preserved in sediments. Using an integrated approach combining lipid biomarkers and radiocarbon dating in particles and sediments, the process of organic carbon recycling and historical changes in its sources and preservation has been examined. A suite of lipid biomarkers in particles and sediments of western Arctic shelves and basins were measured and principle components analysis (PCA) used to allow a robust comparison among the 120+ individual compounds to assign organic sources and relative inputs. Offshore particles from the chlorophyll maximum contained abundant algal markers (e.g. 20:5 and 22:6 FAMEs), low concentrations of terrestrial markers (amyrins and 24-ethylcholest-5-en-3b-ol), and reflected modern 14C values. Particles present in deeper halocline waters also reflect marine production, but a portion of older, terrestrial carbon accompanies the sinking of the spring bloom. Surface and deeper sediments of basins contain older organic carbon and low concentrations of algal biomarkers, suggesting that marine carbon produced in surface waters is rapidly recycled. Taken together, these observations suggest that marine derived organic matter produced in shallow waters fuels carbon cycling, but relatively small amounts are preserved in sediments. As a result, the organic carbon preserved in sediments contrasts sharply to that typically observed in lower latitudes, with an increasing terrestrial signature with distance

Inferring absorbing organic carbon content from AERONET data

Directory of Open Access Journals (Sweden)

A. Arola

2011-01-01

Full Text Available 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 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 mg m⁻² 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 mg m⁻² 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 the global Oslo CTM for several sites. Model values are higher in biomass burning regions than AERONET-based retrievals, while the opposite is true in urban areas in India and China.

Palynofacies assemblages reflect sources of organic matter in New Zealand fjords

Science.gov (United States)

Prebble, Joseph G.; Hinojosa, Jessica L.; Moy, Christopher M.

2018-02-01

Understanding sources and transport pathways of organic carbon in fjord systems is important to quantify carbon cycling in coastal settings. Provenance of surficial sediment organic carbon in Fiordland National Park (southwestern New Zealand) has previously been estimated using a range of techniques, including mixing models derived from stable isotopes and lipid biomarker distributions. Here, we present the first application of palynofacies to explore the sources of particulate organic carbon to five fjords along the SW margin of New Zealand, to further discriminate the provenance of organic carbon in the fjords. We find good correlation between isotopic-and biomarker-derived proxies for organic carbon provenance and our new palynofacies observations. We observe strong down-fjord gradients of decreasing terrestrially derived organic carbon further from the river inflow at fjord heads. Fjords with small catchments and minor fresh water inflow exhibit reversed gradients, indicating that volume of freshwater entering at the fjord head is a primary mechanism to transport particulates down fjord rather than local transport from fjord sides. The palynofacies data also confirmed previously recorded latitudinal trends (i.e. between fjords), of less frequent and more weathered terrestrially derived organic carbon in the southern fjords, consistent with enhanced marine inflow and longer transport times in the southern catchments. Dinocyst assemblages also exhibit a strong latitudinal gradient, with assemblages dominated by heterotrophic forms in the north. In addition to providing support for previous studies, this approach allows finer discrimination of terrestrial organic carbon than previously, for example variation of leaf material. This study demonstrates that visual palynofacies analysis is a valuable tool to pinpoint origins of organic carbon in fjord systems, providing different but complementary information to other proxies.

Sources, Ages, and Alteration of Organic Matter in Estuaries.

Science.gov (United States)

Canuel, Elizabeth A; Hardison, Amber K

2016-01-01

Understanding the processes influencing the sources and fate of organic matter (OM) in estuaries is important for quantifying the contributions of carbon from land and rivers to the global carbon budget of the coastal ocean. Estuaries are sites of high OM production and processing, and understanding biogeochemical processes within these regions is key to quantifying organic carbon (Corg) budgets at the land-ocean margin. These regions provide vital ecological services, including nutrient filtration and protection from floods and storm surge, and provide habitat and nursery areas for numerous commercially important species. Human activities have modified estuarine systems over time, resulting in changes in the production, respiration, burial, and export of Corg. Corg in estuaries is derived from aquatic, terrigenous, and anthropogenic sources, with each source exhibiting a spectrum of ages and lability. The complex source and age characteristics of Corg in estuaries complicate our ability to trace OM along the river-estuary-coastal ocean continuum. This review focuses on the application of organic biomarkers and compound-specific isotope analyses to estuarine environments and on how these tools have enhanced our ability to discern natural sources of OM, trace their incorporation into food webs, and enhance understanding of the fate of Corg within estuaries and their adjacent waters.

Relationship between Organic Carbon Runoff to River and Land Cover

Science.gov (United States)

Kim, G. S.; Lee, S. G.; Lim, C. H.; Lee, W.; Yoo, S.; Kim, S. J.; Heo, S.; Lee, W. K.

2017-12-01

Carbon is an important unit in understanding the ecosystem and energy circulation. Each ecosystem, land, water, and atmosphere, is interconnected through the exchange of energy and organic carbon. In the rivers, primary producers utilize the organic carbon from the land. Understanding the organic carbon uptake into the river is important for understanding the mechanism of river ecosystems. The main organic carbon source of the river is land. However, it is difficult to observe the amount of organic carbon runoff to the river. Therefore, an indirect method should be used to estimate the amount of organic carbon runoff to the river. The organic carbon inflow is caused by the runoff of organic carbon dissolved in water or the inflow of organic carbon particles by soil loss. Therefore, the hydrological model was used to estimate organic carbon runoff through the flow of water. The land cover correlates with soil respiration, soil loss, and so on, and the organic carbon runoff coefficient will be estimated to the river by land cover. Using the organic carbon concentration from water quality data observed at each point in the river, we estimate the amount of organic carbon released from the land. The reason is that the runoff from the watershed converges into the rivers in the watershed, the watershed simulation is conducted based on the water quality data observation point. This defines a watershed that affects organic carbon observation sites. The flow rate of each watershed is calculated by the SWAT (Soil and Water Assessment Tool), and the total organic carbon runoff is calculated by using flow rate and organic carbon concentration. This is compared with the factors related to the amount of organic carbon such as land cover, soil loss, and soil organic carbon, and spatial analysis is carried out to estimate the organic carbon runoff coefficient per land cover.

Organic carbon source in formulated sediments influences life traits and gene expression of Caenorhabditis elegans.

Science.gov (United States)

Franzen, Julia; Menzel, Ralph; Höss, Sebastian; Claus, Evelyn; Steinberg, Christian E W

2012-03-01

River water quality is strongly influenced by their sediments and their associated pollutants. To assess the toxic potential of sediments, sediment toxicity tests require reliable control sediments, potentially including formulated control sediments as one major option. Although some standardization has been carried out, one critical issue still remains the quality of sediment organic matter (SOM). Organic carbon not only binds hydrophobic contaminants, but may be a source of mild toxicity, even if the SOM is essentially uncontaminated. We tested two different sources of organic carbon and the mixture of both (Sphagnum peat (P) and one commercial humic substances preparation-HuminFeed(®), HF) in terms of life trait variables and expression profiles of selected life performance and stress genes of the nematode Caenorhabditis elegans. In synchronous cultures, gene expression profiling was done after 6 and 48 h, respectively. The uncontaminated Sphagnum P reduced growth, but increased numbers of offspring, whereas HF did not significantly alter life trait variables. The 6 h expression profile showed most of the studied stress genes repressed, except for slight to strong induction in cyp-35B1 (all exposures), gst-38 (only mixture), and small hsp-16 genes (all exposures). After 48 h, the expression of almost all studied genes increased, particularly genes coding for antioxidative defense, multiple xenobiotic resistance, vitellogenin-like proteins, and genes regulating lifespan. Overall, even essentially uncontaminated SOM may induce several modes of action on the molecular level in C. elegans which may lead to false results if testing synthetic xenobiotics. This contribution is a plea for a strict standardization of the SOM quality in formulated sediments and to check for corresponding effects in other model sediment organisms, especially if using molecular toxicity endpoints.

Carbon-14 measurements and characterization of dissolved organic carbon in ground water

International Nuclear Information System (INIS)

Murphy, E.M.

1987-01-01

Carbon-14 was measured in the dissolved organic carbon (DOC) in ground water and compared with 14 C analyses of dissolved inorganic carbon (DIC). Two field sites were used for this study; the Stripa mine in central Sweden, and the Milk River Aquifer in southern Alberta, Canada. The Stripa mine consists of a Precambrian granite dominated by fracture flow, while the Milk River Aquifer is a Cretaceous sandstone aquifer characterized by porous flow. At both field sites, 14 C analyses of the DOC provide additional information on the ground-water age. Carbon-14 was measured on both the hydrophobic and hydrophilic organic fractions of the DOC. The organic compounds in the hydrophobic and hydrophilic fractions were also characterized. The DOC may originate from kerogen in the aquifer matrix, from soil organic matter in the recharge zone, of from a combination of these two sources. Carbon-14 analyses, along with characterization of the organics, were used to determine this origin. Carbon-14 analyses of the hydrophobic fraction in the Milk River Aquifer suggest a soil origin, while 14 C analyses of the hydrophilic fraction suggest an origin within the Cretaceous sediments (kerogen) or from the shale in contact with the aquifer

The Nordic Seas carbon budget: Sources, sinks, and uncertainties

OpenAIRE

Jeansson, Emil; Olsen, Are; Eldevik, Tor; Skjelvan, Ingunn; Omar, Abdirahman M.; Lauvset, Siv K.; Nilsen, Jan Even Ø.; Bellerby, Richard G. J; Johannessen, Truls; Falck, Eva

2011-01-01

A carbon budget for the Nordic Seas is derived by combining recent inorganic carbon data from the CARINA database with relevant volume transports. Values of organic carbon in the Nordic Seas' water masses, the amount of carbon input from river runoff, and the removal through sediment burial are taken from the literature. The largest source of carbon to the Nordic Seas is the Atlantic Water that enters the area across the Greenland-Scotland Ridge; this is in particular true for the anthropogen...

Global organic carbon emissions from primary sources from 1960 to 2009

Science.gov (United States)

Huang, Ye; Shen, Huizhong; Chen, Yilin; Zhong, Qirui; Chen, Han; Wang, Rong; Shen, Guofeng; Liu, Junfeng; Li, Bengang; Tao, Shu

2015-12-01

In an attempt to reduce uncertainty, global organic carbon (OC) emissions from a total of 70 sources were compiled at 0.1° × 0.1° resolution for 2007 (PKU-OC-2007) and country scale from 1960 to 2009. The compilation took advantage of a new fuel-consumption data product (PKU-Fuel-2007) and a series of newly published emission factors (EFOC) in developing countries. The estimated OC emissions were 32.9 Tg (24.1-50.6 Tg as interquartile range), of which less than one third was anthropogenic in origin. Uncertainty resulted primarily from variations in EFOC. Asia, Africa, and South America had high emissions mainly because of residential biomass fuel burning or wildfires. Per-person OC emission in rural areas was three times that of urban areas because of the relatively high EFOC of residential solid fuels. Temporal trend of anthropogenic OC emissions depended on rural population, and was influenced primarily by residential crop residue and agricultural waste burning. Both the OC/PM2.5 ratio and emission intensity, defined as quantity of OC emissions per unit of fuel consumption for all sources, of anthropogenic OC followed a decreasing trend, indicating continuous improvement in combustion efficiency and control measures.

Chemical characteristics and source apportionment of fine particulate organic carbon in Hong Kong during high particulate matter episodes in winter 2003

Science.gov (United States)

Li, Yun-Chun; Yu, Jian Zhen; Ho, Steven Sai Hang; Schauer, James J.; Yuan, Zibing; Lau, Alexis K. H.; Louie, Peter K. K.

2013-02-01

PM2.5 samples were collected at six general stations and one roadside station in Hong Kong in two periods of high particulate matter (PM) in 2003 (27 October-4 November and 30 November-13 December). The highest PM2.5 reached 216 μg m- 3 during the first high PM period and 113 μg m- 3 during the second high PM period. Analysis of synoptic weather conditions identified individual sampling days under dominant influence of one of three types of air masses, that is, local, regional and long-range transported (LRT) air masses. Roadside samples were discussed separately due to heavy influences from vehicular emissions. This research examines source apportionment of fine organic carbon (OC) and contribution of secondary organic aerosol on high PM days under different synoptic conditions. Six primary OC (POC) sources (vehicle exhaust, biomass burning, cooking, cigarette smoke, vegetative detritus, and coal combustion) were identified on the basis of characteristic organic tracers. Individual POC source contributions were estimated using chemical mass balance model. In the roadside and the local samples, OC was dominated by the primary sources, accounting for more than 74% of OC. In the samples influenced by regional and LRT air masses, secondary OC (SOC), which was approximated to be the difference between the total measured OC and the apportioned POC, contributed more than 54% of fine OC. SOC was highly correlated with water-soluble organic carbon and sulfate, consistent with its secondary nature.

Accumulation of organic carbon in northwestern Arabian sea sediments

International Nuclear Information System (INIS)

Khan, A.A.

1999-01-01

In this study accumulation of organic carbon in marine sediments of northwestern Arabian sea has been discussed. This paper presents the geochemical analysis of Organic carbon content and accumulation, delta 13 stable carbon isotope and Ba/Al. The primary objective was to investigate the high resolution information about the variations in paleoproductivity and source of organic matter in sediments below an upwelling area. Undisturbed sediments (Piston core NIOP-486) of late Pleistocene time were collected during Netherlands Indian Ocean Program (NIOP-1992-93). The core NIOP-486 was raised from a depth of 2077 meters near the Owen Ridge. This core records deposition history of last 200,000 years and includes 4 warm and 3 cold periods. The distribution of organic carbon content in studied core shows a pronounced cyclicity during glacial and interglacial stages. Organic carbon accumulation trends show that high sedimentation rates in glacial stages results in rapid burial and hence increase organic carbon accumulation. Paleoproductivity indicator Ba/Al has been used to compare with the organic carbon content and is correlated with the warm and cold periods variations in monsoons upwelling intensity. Generally, low paleoproductivity is found in glacial stages. The organic carbon content and accumulation, in sediments however seems to differ from the paleoproductivity trends shown by Ba/Al in glacial sediments of stage 6. Delta 13 C.org isotope results of the core NIOP-486 confirm that organic matter in sediments is predominantly marine (-20 to -23% ). (author)

Dissolved organic carbon in the precipitation of Seoul, Korea: Implications for global wet depositional flux of fossil-fuel derived organic carbon

Science.gov (United States)

Yan, Ge; Kim, Guebuem

2012-11-01

Precipitation was sampled in Seoul over a one-year period from 2009 to 2010 to investigate the sources and fluxes of atmospheric dissolved organic carbon (DOC). The concentrations of DOC varied from 15 μM to 780 μM, with a volume-weighted average of 94 μM. On the basis of correlation analysis using the commonly acknowledged tracers, such as vanadium, the combustion of fossil-fuels was recognized to be the dominant source. With the aid of air mass backward trajectory analyses, we concluded that the primary fraction of DOC in our precipitation samples originated locally in Korea, albeit the frequent long-range transport from eastern and northeastern China might contribute substantially. In light of the relatively invariant organic carbon to sulfur mass ratios in precipitation over Seoul and other urban regions around the world, the global magnitude of wet depositional DOC originating from fossil-fuels was calculated to be 36 ± 10 Tg C yr-1. Our study further underscores the potentially significant environmental impacts that might be brought about by this anthropogenically derived component of organic carbon in the atmosphere.

Organic carbon accumulation and reactivity in central Swedish lakes during the Holocene

Science.gov (United States)

Chmiel, H.; Kokic, J.; Niggemann, J.; Dittmar, T.; Sobek, S.

2012-04-01

Sedimentation and burial of particulate organic carbon (POC), received from terrestrial sources and from lake internal primary production, are responsible for the progressive accumulation and long-term storage of organic matter in lake basins. For lakes in the boreal zone of central Sweden it can be presumed, that the onset of POC accumulation occurred during the early Holocene (˜8000 BP.) after the retreat of the Scandinavian ice sheet. In this study we investigated carbon mass accumulation rates (CMARs), as well as sources and reactivity of deposited organic material, for seven lakes in central Sweden (60°N, 15°E), in order to obtain a detailed temporal resolution of carbon burial and preservation in boreal lakes. Sediment long-cores were sampled in March 2011 from the ice, and CMARs were calculated from water contents, dry bulk densities, carbon contents and radiocarbon (14C) ages of the depth profiles. To indicate the sources of the organic material and characterize its diagenetic state, we determined carbon-nitrogen ratios (C/N) as well as amounts and compositions of lignin phenols. The transitions from organic rich sediment layers to glacial till deposits were found to be in sediment depths of ˜3 m in each lake. POC contents were on average highest (25-34 wt. % C), in small lakes (≤ 0.07 km2) and lowest (10-18 wt. % C) in the larger lakes (≥ 165 km2). The CMARs over the Holocene showed significant variations and were on average lower in the early Holocene, compared to recent accumulation rates. C/N values and the composition of lignin phenols further provided indications of important changes in organic matter source and reactivity over the Holocene. In summary, our data suggest that boreal lake sediments were a significantly stronger sink for organic carbon during the last ~150 years than during earlier periods of the Holocene.

Identifying sources of dissolved organic carbon in agriculturally dominated rivers using radiocarbon age dating: Sacramento-San Joaquin River Basin, California

Science.gov (United States)

Sickman, James O.; DiGiorgio, Carol L.; Davisson, M. Lee; Lucero, Delores M.; Bergamaschi, Brian A.

2010-01-01

We used radiocarbon measurements of dissolved organic carbon (DOC) to resolve sources of riverine carbon within agriculturally dominated landscapes in California. During 2003 and 2004, average Δ14C for DOC was −254‰ in agricultural drains in the Sacramento–San Joaquin Delta, −218‰ in the San Joaquin River, −175‰ in the California State Water Project and −152‰ in the Sacramento River. The age of bulk DOC transiting the rivers of California’s Central Valley is the oldest reported for large rivers and suggests wide-spread loss of soil organic matter caused by agriculture and urbanization. Using DAX 8 adsorbent, we isolated and measured 14C concentrations in hydrophobic acid fractions (HPOA); river samples showed evidence of bomb-pulse carbon with average Δ14C of 91 and 76‰ for the San Joaquin and Sacramento Rivers, respectively, with older HPOA, −204‰, observed in agricultural drains. An operationally defined non-HPOA fraction of DOC was observed in the San Joaquin River with seasonally computed Δ14C values of between −275 and −687‰; the source of this aged material was hypothesized to be physically protected organic-matter in high clay-content soils and agrochemicals (i.e., radiocarbon-dead material) applied to farmlands. Mixing models suggest that the Sacramento River contributes about 50% of the DOC load in the California State Water Project, and agricultural drains contribute approximately one-third of the load. In contrast to studies showing stabilization of soil carbon pools within one or two decades following land conversion, sustained loss of soil organic matter, occurring many decades after the initial agricultural-land conversion, was observed in California’s Central Valley.

Effects of organic nitrogen and carbon sources on mycelial growth ...

African Journals Online (AJOL)

Grifola umbellate is a famous and expensive Chinese herb medicine and the main medicinal component is polysaccharide mainly produced by its mycelia. Effects of organic nitrogen and carbon resources on mycelial growth and polysaccharides production of a medicinal mushroom, G. umbellate were studied in the ...

Storage and release of organic carbon from glaciers and ice sheets

Science.gov (United States)

Hood, Eran; Battin, Tom J.; Fellman, Jason; O'Neel, Shad; Spencer, Robert G. M.

2015-02-01

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.

Storage and release of organic carbon from glaciers and ice sheets

Science.gov (United States)

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.

Determining Inorganic and Organic Carbon.

Science.gov (United States)

Koistinen, Jaana; Sjöblom, Mervi; Spilling, Kristian

2017-11-21

Carbon is the element which makes up the major fraction of lipids and carbohydrates, which could be used for making biofuel. It is therefore important to provide enough carbon and also follow the flow into particulate organic carbon and potential loss to dissolved organic forms of carbon. Here we present methods for determining dissolved inorganic carbon, dissolved organic carbon, and particulate organic carbon.

Organic carbon source and salinity shape sediment bacterial composition in two China marginal seas and their major tributaries.

Science.gov (United States)

Wang, Kai; Zou, Li; Lu, Xinxin; Mou, Xiaozhen

2018-08-15

Marginal sea sediments receive organic substrates of different origins, but whether and to what extent sediment microbial communities are reflective of the different sources of organic substrates remain unclear. To address these questions, sediment samples were collected in two connected China marginal seas, i.e., Bohai Sea and Yellow Sea, and their two major tributaries (Yellow River and Liao River). Sediment bacterial community composition (BCC) was examined using 16S rRNA gene pyrosequencing. In addition, physicochemical variables that describe environmental conditions and sediment features were measured. Our results revealed that BCCs changed with salinity and organic carbon (OC) content. Members of Gaiellaceae and Comamonadaceae showed a rapid decrease as salinity and phytoplankton-derived OC increased, while Piscirickettsiaceae and Desulfobulbaceae exhibited an opposite distribution pattern. Differences of riverine vs. marginal sea sediment BCCs could be mostly explained by salinity. However, within the marginal seas, sediment BCC variations were mainly explained by OC-related variables, including terrestrial-derived fatty acids (Terr_FA), phytoplankton-derived polyunsaturated fatty acids (Phyto_PUFA), stable carbon isotopes (δ 13 C), and carbon to nitrogen ratio (C/N). In addition to environmental variables, network analysis suggested that interactions among individual bacterial taxa might be important in shaping sediment BCCs in the studied areas. Copyright © 2018 Elsevier B.V. All rights reserved.

Organic Carbon Sources and their Transfer in a Gulf of Mexico Coral Reef Ecosystem under River Influence

Science.gov (United States)

Parrish, C.; Carreón-Palau, L.; del Ángel-Rodríguez, J.; Perez-Espana, H.; Aguiniga-Garcıa, S.

2016-02-01

To assess the degree to which coral reefs in a marine protected area have been influenced by terrestrial and anthropogenic organic carbon inputs we used C and N stable isotopes and lipid biomarkers in the Coral Reef System of Veracruz in the southwest Gulf of Mexico. A C and N stable isotope mixing model and a calculated fatty acid (FA) retention factor revealed the primary producer sources that fuel the coral reef food web. Then lipid classes, FA and sterol biomarkers determined production of terrestrial and marine biogenic material of nutritional quality to pelagic and benthic organisms. Finally, coprostanol determined pollutant loading from sewage in the suspended particulate matter. Results indicate that phytoplankton is the major source of essential FA for fish and that dietary energy from terrestrial sources such as mangroves are transferred to juvenile fish, while sea grass non-essential FA are transferred to the entire food web. Sea urchins may be the main consumers of brown macroalgae, while surgeon fish prefer red algae. C and N isotopic values and the C:N ratio suggest that fertilizer is the principal source of nitrogen to macroalgae. Thus nitrogen supply also favored phytoplankton and sea grass growth leading to a better nutritional condition and high retention of organic carbon in the food web members during the rainy season when river influence increases. However, the great star coral Montastrea cavernosa nutritional condition decreased significantly. The nearest river to the Reef System was polluted in the dry season; however, a dilution effect was detected in the rainy season, when some coral reefs were contaminated. In 2013, a new treatment plant started working in the area. We would suggest monitoring δ15N and the C: N ratio in macroalgae as indicators of the nitrogen input and coprostanol as an indicator of human feces pollution in order to verify the efficiency of the new treatment plant as part of the management program of the Reef System.

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

Science.gov (United States)

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

2015-08-06

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.

Elemental and stable isotopic approaches for studying the organic and inorganic carbon components in natural samples

International Nuclear Information System (INIS)

Helie, J-F

2009-01-01

The carbon cycle is an important part of major biogeochemical cycles. Many techniques may be used to characterize carbon amounts and sources in the environment. Here we first review the most popular techniques for the determination of organic and inorganic carbon concentrations. Decarbonatation techniques are also reviewed in details since it is often an important part of organic carbon analysis. The second part of this paper addresses the use of carbon stable isotopes to characterize organic carbon sources and processes in the environment. An overview of general stable isotopes background and terminology is given as well as the most popular analytical techniques.

Aged riverine particulate organic carbon in four UK catchments

International Nuclear Information System (INIS)

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

2015-01-01

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, PO 14 C 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 PO 14 C value for the 7 sites of 91.2 pMC corresponded to an average age of 680 14 C 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 PO 14 C 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- 14 C topsoil organic matter by mineralisation during riverine transport. The significantly lower average PO 14 C 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 PO 14 C in rivers draining catchments with low erosion rates. - Highlights: �

Organic composition and source apportionment of fine aerosol at Monterrey, Mexico, based on organic markers

Directory of Open Access Journals (Sweden)

Y. Mancilla

2016-01-01

Full Text Available Primary emissions from anthropogenic and biogenic sources as well as secondary formation are responsible for the pollution levels of ambient air in major urban areas. These sources release fine particles into the air that negatively impact human health and the environment. Organic molecular markers, which are compounds that are unique to specific PM2.5 sources, can be utilized to identify the major emission sources in urban areas. In this study, 43 representative PM2.5 samples, for both daytime and nighttime periods, were built from individual samples collected in an urban site of the Monterrey metropolitan area (MMA during the spring and fall of 2011 and 2012. The samples were analyzed for organic carbon, elemental carbon, and organic molecular markers. Several diagnostic tools were employed for the preliminary identification of emission sources. Organic compounds for eight compound classes were quantified. The n-alkanoic acids were the most abundant, followed by n-alkanes, wood smoke markers, and levoglucosan/alkenoic acids. Polycyclic aromatic hydrocarbons (PAHs and hopanes were less abundant. The carbon preference index (0.7–2.6 for n-alkanes indicates a major contribution of anthropogenic and mixed sources during the fall and the spring, respectively. Hopanes levels confirmed the contribution from gasoline and diesel engines. In addition, the contribution of gasoline and diesel vehicle exhaust was confirmed and identified by the PAH concentrations in PM2.5. Diagnostic ratios of PAHs showed emissions from burning coal, wood, biomass, and other fossil fuels. The total PAHs and elemental carbon were correlated (r2 =  0.39–0.70 across the monitoring periods, reinforcing that motor vehicles are the major contributors of PAHs. Cholesterol levels remained constant during the spring and fall, showing evidence of the contribution of meat-cooking operations, while the isolated concentrations of levoglucosan suggested occasional biomass

Dynamics of organic and inorganic carbon across contiguous mangrove and seagrass systems (Gazi Bay, Kenya)

NARCIS (Netherlands)

Bouillon, S.; Dehairs, F.; Velimirov, B.; Abril, G.; Borges, A.V.

2007-01-01

We report on the water column biogeochemistry in adjacent mangrove and seagrass systems in Gazi Bay (Kenya), with a focus on assessing the sources and cycling of organic and inorganic carbon. Mangrove and seagrass-derived material was found to be the dominant organic carbon sources in the water

Determination of the growth of nematophagous fungi on diverse carbon sources

Directory of Open Access Journals (Sweden)

Martha Orozco

2015-11-01

Full Text Available Organic amendments have been widely used to stimulate the populations of predatory nematophagous fungi (PNF in soil; however, the use of organic amendments has produced inconsistent results in the control of parasitic nematodes. The inconsistencies have been partially attributed to the chemical composition of the organic amendments, specifically to carbon and nitrogen contents. Therefore, to know the carbon preferences of these fungi could be helpful to promote the predatory phase of the PNF in soil. The aim of this study was to determine the growth of native PNF strains from Costa Rica in diverse carbon sources. The PNF Arthrobotrys oligospora and Candelabrella musiformis were grown in artificial culture media containing the following carbon sources: cellulose, chitin, pectin, starch, and skim milk. The growth rate developed by the PNF in each one of the culture media was determined and compared. The growth rates developed by both fungal species followed the next order: cellulos e>chitin>pectin>starch>skim milk. Significant differences in the growth rates developed by the fungal strains were detected only in culture medium containing cellulose, in comparison with culture media containing other carbon sources. In culture medium containing cellulose both A. oligospora and C. musiformis grew faster with respect to the other culture media, but A. oligospora strains grew faster in comparison with C. musiformis strains. Both fungal species developed the lowest growth rates in culture media containing starch and skim milk.

Badlands and the Carbon cycle: a significant source of petrogenic organic carbon in rivers and marine environments?

Science.gov (United States)

Copard, Yoann; Eyrolle-Boyer, Frederique; Radakovitch, Olivier; Poirel, Alain; Raimbault, Patrick; Lebouteiller, Caroline; Gairoard, Stéphanie; Di-Giovanni, Christian

2016-04-01

A key issue in the study of carbon biogeochemical cycle is to well constrain each carbon origin in term of fluxes between all C-reservoirs. From continental surfaces to oceans, rivers convey particulate organic carbon originate from the biomass (biospheric OC) and /or from the sedimentary rocks (petrogenic OC). Existence and importance of this petrogenic OC export to oceans was debated for several decades (see Copard et al., 2007 and ref.), but it is now assumed that 20% of the global carbon export to ocean has a geological origin (Galy et al., 2015). The main current challenge is to constrain the major contributors to this petrogenic OC flux. Amongst the expected sedimentary sources of petrogenic OC in rivers, sedimentary rocks forming badlands can be rightly considered as some viable candidates. Indeed these rocks show a strong erosion rate, may exceed 50 kt km-2 y-1 and in addition, shales, marls and argillaceous rocks, frequently forming badlands (see Nadal-Romero et al., 2011 for the Mediterranean area), contain a significant amount of petrogenic OC (frequently over 0.50 wt. %, Ronov and Yaroshevsky 1976). Our work illustrates the contribution of badlands, mainly distributed within the Durance catchment (a main tributary of the Rhône river), in the petrogenic OC export to the Mediterranean Sea. The approach is based on (i) the use of previous and new data on radiogenic carbon, (ii) bulk organic geochemistry (Rock-Eval pyrolysis), (iii) optical quantification of particulate OM (palynofacies), performed on suspended sediments from the Durance, the Rhône rivers and from small rivers draining the badlands. A mean erosion rate of badlands, previously calculated for instrumented catchments (SOERE Draix-Bléone, Graz et al., 2012) was also applied to the badlands disseminated within the Durance catchment. These different methodologies converge to a petrogenic contribution of the OC export to the Mediterranean Sea close to 30 %. Badlands from the Durance catchment

[Sources of dissolved organic carbon and the bioavailability of dissolved carbohydrates in the tributaries of Lake Taihu].

Science.gov (United States)

Ye, Lin-Lin; Wu, Xiao-Dong; Kong, Fan-Xiang; Liu, Bo; Yan, De-Zhi

2015-03-01

Surface water samples of Yincungang and Chendonggang Rivers were collected from September 2012 to August 2013 in Lake Taihu. Water temperature, Chlorophyll a and bacterial abundance were analyzed, as well as dissolved organic carbon (DOC) concentrations, stable carbon isotope of DOC (Δ13C(DOC)), specific UV absorbance (SUVA254 ) and dissolved carbohydrates concentrations. Δ13C(DOC) ranged from -27.03% per thousand ± 0.30% per thousand to -23.38%per thousand ± 0.20% per thousand, indicating a terrestrial source. Both the autochthonous and allochthonous sources contributed to the carbohydrates pool in the tributaries. Significant differences in PCHO (polysaccharides) and MCHO (monosaccharides) concentrations were observed between spring-summer and autumn-winter (P carbohydrates. PCHO contributed a major fraction to TCHO (total dissolved carbohydrates) in autumn and winter, which could be explained by the accumulation of undegradable PCHO limited by the low water temperature; MCHO contributed a major fraction to TCHO in spring and summer, which might be caused by the transformation from PCHO by microbes at high water temperature.

BIOREMEDIATION FOR ACID MINE DRAINAGE: ORGANIC SOLID WASTE AS CARBON SOURCES FOR SULFATE-REDUCING BACTERIA: A REVIEW

Directory of Open Access Journals (Sweden)

I. N. Jamil

2013-12-01

Full Text Available Biological sulfate reduction has been slowly replacing chemical unit processes to treat acid mine drainage (AMD. Bioremediations for AMD treatment are favored due to their low capital and maintenance cost. This paper describes the available AMD treatment, current SRB commercialization such as THIOPAQ® and BioSulphide® technologies, and also the factors and limitations faced. THIOPAQ® and BioSulphide® technologies use expensive carbon sources such as hydrogen as the electron donor. This paper discusses the possibility of organic solid waste as an alternative substrate as it is cheaper and abundant. A possible AMD treatment system setup was also proposed to test the efficiency of sulfate-reducing bacteria utilizing organic solid substrate.

Seasonal variability of organic matter composition in an Alaskan glacier outflow: insights into glacier carbon sources

International Nuclear Information System (INIS)

Spencer, Robert G M; Vermilyea, Andrew; Fellman, Jason; Hood, Eran; Raymond, Peter; Stubbins, Aron; Scott, Durelle

2014-01-01

Glacier ecosystems are a significant source of bioavailable, yet ancient dissolved organic carbon (DOC). Characterizing DOC in Mendenhall Glacier outflow (southeast Alaska) we document a seasonal persistence to the radiocarbon-depleted signature of DOC, highlighting ancient DOC as a ubiquitous feature of glacier outflow. We observed no systematic depletion in Δ 14 C-DOC with increasing discharge during the melt season that would suggest mobilization of an aged subglacial carbon store. However, DOC concentration, δ 13 C-DOC, Δ 14 C-DOC and fluorescence signatures appear to have been influenced by runoff from vegetated hillslopes above the glacier during onset and senescence of melt. In the peak glacier melt period, the Δ 14 C-DOC of stream samples at the outflow (−181.7 to −355.3‰) was comparable to the Δ 14 C-DOC for snow samples from the accumulation zone (−207.2 to −390.9‰), suggesting that ancient DOC from the glacier surface is exported in glacier runoff. The pre-aged DOC in glacier snow and runoff is consistent with contributions from fossil fuel combustion sources similar to those documented previously in ice cores and thus provides evidence for anthropogenic perturbation of the carbon cycle. Overall, our results emphasize the need to further characterize DOC inputs to glacier ecosystems, particularly in light of predicted changes in glacier mass and runoff in the coming century. (papers)

New views on "old" carbon in the Amazon River: Insight from the source of organic carbon eroded from the Peruvian Andes

Science.gov (United States)

Clark, K. E.; Hilton, R. G.; West, A. J.; Malhi, Y.; Gröcke, D. R.; Bryant, C. L.; Ascough, P. L.; Robles Caceres, A.; New, M.

2013-05-01

rivers play a key role in the delivery of particulate organic carbon (POC) to large river systems and the ocean. Due to the extent of its drainage area and runoff, the Amazon River is one of Earth's most important biogeochemical systems. However, the source of POC eroded from the humid region of the Eastern Andes and the input of fossil POC from sedimentary rocks (POCfossil) remains poorly constrained. Here we collected suspended sediments from the Kosñipata River during flood events to better characterize Andean POC, measuring the nitrogen to organic carbon ratio (N/C), stable carbon isotopes (δ13Corg) and radiocarbon (Δ14Corg). Δ14Corg values ranged from -711‰ to -15‰, and significant linear trends between Δ14Corg, N/C and δ13Corg suggested that this reflects the mixing of POCfossil with very young organic matter (Δ14Corg 50‰) from the terrestrial biosphere (POCnon-fossil). Using N/C and Δ14Corg in an end-member mixing analysis, we quantify the fraction of POCfossil (to within 0.1) and find that it contributes a constant proportion of the suspended sediment mass (0.37 ± 0.03%) and up to 80% of total POC. In contrast, the relative contribution of POCnon-fossil was variable, being most important during the rising limb and peak discharges of flood events. The new data shed light on published measurements of "old" POC (low Δ14Corg) in Andean-fed tributaries of the Amazon River, with their Δ14Corg and δ13Corg values consistent with variable addition of POCfossil. The findings suggest a greater persistence of Andean POC in the lowland Amazon than previously recognized.

Assimilation of aged organic carbon in a glacial river food web

Science.gov (United States)

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

Sources and fate of organic (DOC, POC, CDOM) and inorganic (DIC) carbon in a mangrove dominated estuary (French Guiana)

Science.gov (United States)

Ray, R.; Michaud, E.; Vantrepotte, V.; Aller, R. C.; Morvan, S.; Thouzeau, G.

2016-12-01

We studied the mangrove dominated Sinnamary estuarine system in French Guiana during the dry and wet seasons in 2015 to examine the sources, transport and fate of surface water DOC, POC and DIC along the salinity gradient and the effect of tidal fluctuations on carbon dynamics. Elemental ratios, stable isotopes and optical properties (absorption) were applied as proxies to delineate the sources and molecular structure of the organic carbon. Results showed that during the wet season there were significant net inputs of POC and DOC along the salinity gradient from mangroves and enhanced surface runoff. Time series performed during the dry season at a station in channel water adjacent to mangroves revealed mangrove-derived export and exchanges of DOC and POC during the ebb and marine algae import during the flood. DOC was the dominant form of carbon in both seasons with DOC:POC ratios typically between 13 and 40. Both δ13DOC and CDOM descriptors (e.g., S275-295 and a*412) confirmed mangrove litter leaching to be the primary contributor of high molecular weight dissolved organic matter in the wet season which was replaced by marine phytoplanktonic OC during transport offshore in the dry season. CDOM aromaticity is lower in the dry season as mangrove inputs decrease. POC showed similar trends as DOC, with maximum contributions of terrestrial litter in the river and mixing zone, and in situ production dominant in the marine zone. The entire estuary is heterotrophic, exhibiting high pCO2 (837-5575µatm) and oxygen undersaturation (59-86%) in both seasons, and substantial CO2 emission fluxes (278-3671mmol m-2 d-1). Intense local remineralization and laterally transported CO2 originating from mangrove benthic respiration could account for the water column pCO2 enrichment during low tide and night time. Keywords: Organic carbon, stable isotopes, CDOM, pCO2, mangrove, French Guiana

Stable isotope compositions of organic carbon and contents of ...

African Journals Online (AJOL)

The stable isotope compositions of organic carbon (OC), and contents of OC and nitrogen for four sediment cores recovered from lakes Makat (located in the Ngorongoro Crater), Ndutu and Masek (located in the Serengeti Plains) are used to document sources of organic matter (OM) and climatic changes in sub-arid ...

Aged riverine particulate organic carbon in four UK catchments

Energy Technology Data Exchange (ETDEWEB)

Adams, Jessica L., E-mail: jesams@ceh.ac.uk [Centre for Ecology and Hydrology, Lancaster Environment Centre, Lancaster, LA1 4AP (United Kingdom); Tipping, Edward, E-mail: et@ceh.ac.uk [Centre for Ecology and Hydrology, Lancaster Environment Centre, Lancaster, LA1 4AP (United Kingdom); Bryant, Charlotte L., E-mail: charlotte.bryant@glasgow.ac.uk [NERC Radiocarbon Facility, East Kilbride G75 0QF, Scotland (United Kingdom); Helliwell, Rachel C., E-mail: rachel.helliwell@hutton.ac.uk [The James Hutton Institute, Craigiebuckler, Aberdeen AB15 8QH Scotland (United Kingdom); Toberman, Hannah, E-mail: hannahtoberman@hotmail.com [Centre for Ecology and Hydrology, Lancaster Environment Centre, Lancaster, LA1 4AP (United Kingdom); School of Environmental Sciences, University of Liverpool, Liverpool L69 3GP (United Kingdom); Quinton, John, E-mail: j.quinton@lancaster.ac.uk [Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ (United Kingdom)

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, PO{sup 14}C 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 PO{sup 14}C value for the 7 sites of 91.2 pMC corresponded to an average age of 680 {sup 14}C 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 PO{sup 14}C 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-{sup 14}C topsoil organic matter by mineralisation during riverine transport. The significantly lower average PO{sup 14}C 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 PO{sup 14}C in rivers draining catchments with low erosion rates

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

Science.gov (United States)

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

Primary Nutritional Content of Bio-Flocs Cultured with Different Organic Carbon Sources and Salinity

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JULIE EKASARI

2010-09-01

Full Text Available Application of bio-flocs technology (BFT in aquaculture offers a solution to avoid environmental impact of high nutrient discharges and to reduce the use of artificial feed. In BFT, excess of nutrients in aquaculture systems are converted into microbial biomass, which can be consumed by the cultured animals as a food source. In this experiment, upconcentrated pond water obtained from the drum filter of a freshwater tilapia farm was used for bio-flocs reactors. Two carbon sources, sugar and glycerol, were used as the first variable, and two different levels of salinity, 0 and 30 ppt, were used as the second variable. Bio-flocs with glycerol as a carbon source had higher total n-6 PUFAs (19.1 ± 2.1 and 22.3 ± 8.6 mg/g DW at 0 and 30 ppt, respectively than that of glucose (4.0 ± 0.1 and 12.6 ± 2.5 mg/g DW at 0 and 30 ppt. However, there was no effect of carbon source or salinity on crude protein, lipid, and total n-3 PUFAs contents of the bio-flocs.

Sources and characteristics of terrestrial carbon in Holocene-scale sediments of the East Siberian Sea

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Keskitalo, Kirsi; Tesi, Tommaso; Bröder, Lisa; Andersson, August; Pearce, Christof; Sköld, Martin; Semiletov, Igor P.; Dudarev, Oleg V.; Gustafsson, Örjan

2017-09-01

Thawing of permafrost carbon (PF-C) due to climate warming can remobilise considerable amounts of terrestrial carbon from its long-term storage to the marine environment. PF-C can be then be buried in sediments or remineralised to CO2 with implications for the carbon-climate feedback. Studying historical sediment records during past natural climate changes can help us to understand the response of permafrost to current climate warming. In this study, two sediment cores collected from the East Siberian Sea were used to study terrestrial organic carbon sources, composition and degradation during the past ˜ 9500 cal yrs BP. CuO-derived lignin and cutin products (i.e., compounds solely biosynthesised in terrestrial plants) combined with δ13C suggest that there was a higher input of terrestrial organic carbon to the East Siberian Sea between ˜ 9500 and 8200 cal yrs BP than in all later periods. This high input was likely caused by marine transgression and permafrost destabilisation in the early Holocene climatic optimum. Based on source apportionment modelling using dual-carbon isotope (Δ14C, δ13C) data, coastal erosion releasing old Pleistocene permafrost carbon was identified as a significant source of organic matter translocated to the East Siberian Sea during the Holocene.

Effects of organic carbon source and light-dark period on growth and lipid accumulation of Scenedesmus sp. AARL G022

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Doungpen Dittamart

2014-08-01

Full Text Available The levels of different organic carbon supplements in a mixotrophic culture were optimised to enhance biomass and lipid accumulation in Scenedesmus sp. AARL G022. The supplement nutrients, viz. glucose, glycerol and sodium acetate, were compared with non-organic carbon supplement (photoautotrophic culture. The most suitable carbon source was found to be 0.05M glucose, giving a yield of 2.78 ± 0.86 g.L -1 of biomass and 233.68 ± 35.34 mg.L -1 of crude lipid. The highest yield of biomass (4.04 ± 0.36 g.L -1 was obtained from a light-dark cycle of 24:0 hr. The highest crude lipid yield of 396.35 ± 11.60 mg.L -1 was obtained from a light-dark cycle of 16:8 hr. The optimised condition for culturing Scenedesmus sp. AARL G022 is to cultivate it under a mixotrophic condition using 0.05M of glucose supplement with a light-dark cycle of 16:8 hr.

Tracking Organic Carbon Transport From the Stordalen Mire to Glacial Lake Tornetrask, Abisko, Sweden

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Beck, M. A.; Hamilton, B. T.; Spry, E.; Johnson, J. E.; Palace, M. W.; McCalley, C. K.; Varner, R. K.; Bothner, W. A.

2016-12-01

In subarctic regions, labile organic carbon from thawing permafrost and productivity of terrestrial and aquatic vegetation are sources of carbon to lake sediments. Methane is produced in lake sediments from the decomposition of organic carbon at rates affected by vegetation presence and type as well as sediment temperature. Recent research in the Stordalen Mire in northern Sweden has suggested that labile organic carbon sources in young, shallow lake sediments yield the highest in situ sediment methane concentrations. Ebullition (or bubbling) of this methane is predominantly controlled by seasonal warming. In this project we sampled stream, glacial and post-glacial lake sediments along a drainage transect through the Stordalen Mire into the large glacial Lake Torneträsk. Our results indicate that the highest methane and total organic carbon (TOC) concentrations were observed in lake and stream sediments in the upper 25 centimeters, consistent with previous studies. C/N ratios range from 8 to 32, and suggest that a mix of aquatic and terrestrial vegetation sources dominate the sedimentary record. Although water transport occurs throughout the mire, major depositional centers for sediments and organic carbon occur within the lakes and prohibit young, labile TOC from entering the larger glacial Lake Torneträsk. The lack of an observed sediment fan at the outlet of the Mire to the lake is consistent with this observation. Our results suggest that carbon produced in the mire stays in the mire, allowing methane production to be greater in the mire bound lakes and streams than in the larger adjacent glacial lake.

[Kinetic simulation of enhanced biological phosphorus removal with fermentation broth as carbon source].

Science.gov (United States)

Zhang, Chao; Chen, Yin-Guang

2013-07-01

As a high-quality carbon source, fermentation broth could promote the phosphorus removal efficiency in enhanced biological phosphorus removal (EBPR). The transformation of substrates in EBPR fed with fermentation broth was well simulated using the modified activated sludge model No. 2 (ASM2) based on the carbon source metabolism. When fermentation broth was used as the sole carbon source, it was found that heterotrophic bacteria acted as a promoter rather than a competitor to the phosphorus accumulating organisms (PAO). When fermentation broth was used as a supplementary carbon source of real municipal wastewater, the wastewater composition was optimized for PAO growth; and the PAO concentration, which was increased by 3.3 times compared to that in EBPR fed with solely real municipal wastewater, accounting for about 40% of the total biomass in the reactor.

Partitioning of fluorotelomer alcohols to octanol and different sources of dissolved organic carbon.

Science.gov (United States)

Carmosini, Nadia; Lee, Linda S

2008-09-01

Interest in the environmental fate of fluorotelomer alcohols (FTOHs) has spurred efforts to understand their equilibrium partitioning behavior. Experimentally determined partition coefficients for FTOHs between soil/water and air/water have been reported, but direct measurements of partition coefficients for dissolved organic carbon (DOC)/water (K(doc)) and octanol/ water(K(ow)) have been lacking. Here we measured the partitioning of 8:2 and 6:2 FTOH between one or more types of DOC and water using enhanced solubility or dialysis bag techniques, and also quantified K(ow) values for 4:2 to 8:2 FTOH using a batch equilibration method. The range in measured log K(doc) values for 8:2 FTOH using the enhanced solubility technique with DOC derived from two soils, two biosolids, and three reference humic acids is 2.00-3.97 with the lowest values obtained for the biosolids and an average across all other DOC sources (biosolid DOC excluded) of 3.54 +/- 0.29. For 6:2 FTOH and Aldrich humic acid, a log K(doc) value of 1.96 +/- 0.45 was measured using the dialysis technique. These average values are approximately 1 to 2 log units lower than previously indirectly estimated K(doc) values. Overall, the affinity for DOC tends to be slightly lower than that for particulate soil organic carbon. Measured log K(ow) values for 4:2 (3.30 +/- 0.04), 6:2 (4.54 +/- 0.01), and 8:2 FTOH (5.58 +/- 0.06) were in good agreement with previously reported estimates. Using relationships between experimentally measured partition coefficients and C-atom chain length, we estimated K(doc) and K(ow) values for shorter and longer chain FTOHs, respectively, that we were unable to measure experimentally.

Comparing carbon to carbon: Organic and inorganic carbon balances across nitrogen fertilization gradients in rainfed vs. irrigated Midwest US cropland

Science.gov (United States)

Hamilton, S. K.; McGill, B.

2017-12-01

The top meter of the earth's soil contains about twice the amount of carbon than the atmosphere. Agricultural management practices influence whether a cropland soil is a net carbon source or sink. These practices affect both organic and inorganic carbon cycling although the vast majority of studies examine the former. We will present results from several rarely-compared carbon fluxes: carbon dioxide emissions and sequestration from lime (calcium carbonate) weathering, dissolved gases emitted from groundwater-fed irrigation, dissolved organic carbon (DOC) leaching to groundwater, and soil organic matter storage. These were compared in a corn-soybean-wheat rotation under no-till management across a nitrogen fertilizer gradient where half of the replicated blocks are irrigated with groundwater. DOC and liming fluxes are also estimated from a complementary study in neighboring plots comparing a gradient of management practices from conventional to biologically-based annuals and perennials. These studies were conducted at the Kellogg Biological Station Long Term Ecological Research site in Michigan where previous work estimated that carbon dioxide emissions from liming accounted for about one quarter of the total global warming impact (GWI) from no-till systems—our work refines that figure. We will present a first time look at the GWI of gases dissolved in groundwater that are emitted when the water equilibrates with the atmosphere. We will explore whether nitrogen fertilizer and irrigation increase soil organic carbon sequestration by producing greater crop biomass and residues or if they enhance microbial activity, increasing decomposition of organic matter. These results are critical for more accurately estimating how intensive agricultural practices affect the carbon balance of cropping systems.

An assessment, using stable isotopes, of the importance of allochthonous organic carbon sources to the pelagic food web in Loch Ness

Science.gov (United States)

Jones, R. I.; Grey, J.; Sleep, D.; Quarmby, C.

1998-01-01

The natural abundance of stable isotopes (δ13C and δ1315N) was determined for components of the pelagic food web in Loch Ness, a deep oligotrophic lake in northern Scotland, and compared with values from the inflow rivers and the catchment vegetation. Phytoplankton δ13C was low compared to values reported from other lakes, possibly reflecting a high use of 13C-depleted carbon dioxide from respired organic matter before further isotopic fractionation during photosynthesis. Phytoplankton δ13C was appreciably lower than that of dissolved and particulate organic matter (DOM and POM) in the loch. The DOM and POM were evidently overwhelmingly of allochthonous origin and ultimately derived from terrestrial plant detritus. The distinctive δ13C values for phytoplankton and detritus in the loch allowed the use of food sources by grazing crustacean zooplankton to be assessed, and the contributions of phytoplankton carbon and detrital carbon to zooplankton total body carbon appeared to be about equal. Comparison of δ13C and δ15N values for zooplankton and fish allowed assessment of trophic structure in the loch. The very high dependence of the pelagic food web in Loch Ness on allochthonous organic matter inputs from the catchment may be exceptional in a large lake, but has important implications for our understanding of lake ecosystem processes as well as for lake management.

Effects of organic nitrogen and carbon sources on mycelial growth ...

African Journals Online (AJOL)

STORAGESEVER

2009-10-19

Oct 19, 2009 ... mycelial growth and polysaccharides production and their optimization in the ... Soybean meal was selected as the optimal organic nitrogen source for its significant ..... economy and high yield in industrial production. There-.

Carbon isotopes of dissolved inorganic carbon reflect utilization of different carbon sources by microbial communities in two limestone aquifer assemblages

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M. E. Nowak

2017-08-01

Full Text Available Isotopes of dissolved inorganic carbon (DIC are used to indicate both transit times and biogeochemical evolution of groundwaters. These signals can be complicated in carbonate aquifers, as both abiotic (i.e., carbonate equilibria and biotic factors influence the δ13C and 14C of DIC. We applied a novel graphical method for tracking changes in the δ13C and 14C of DIC in two distinct aquifer complexes identified in the Hainich Critical Zone Exploratory (CZE, a platform to study how water transport links surface and shallow groundwaters in limestone and marlstone rocks in central Germany. For more quantitative estimates of contributions of different biotic and abiotic carbon sources to the DIC pool, we used the NETPATH geochemical modeling program, which accounts for changes in dissolved ions in addition to C isotopes. Although water residence times in the Hainich CZE aquifers based on hydrogeology are relatively short (years or less, DIC isotopes in the shallow, mostly anoxic, aquifer assemblage (HTU were depleted in 14C compared to a deeper, oxic, aquifer complex (HTL. Carbon isotopes and chemical changes in the deeper HTL wells could be explained by interaction of recharge waters equilibrated with post-bomb 14C sources with carbonates. However, oxygen depletion and δ13C and 14C values of DIC below those expected from the processes of carbonate equilibrium alone indicate considerably different biogeochemical evolution of waters in the upper aquifer assemblage (HTU wells. Changes in 14C and 13C in the upper aquifer complexes result from a number of biotic and abiotic processes, including oxidation of 14C-depleted OM derived from recycled microbial carbon and sedimentary organic matter as well as water–rock interactions. The microbial pathways inferred from DIC isotope shifts and changes in water chemistry in the HTU wells were supported by comparison with in situ microbial community structure based on 16S rRNA analyses. Our findings

Evidence for the assimilation of ancient glacier organic carbon in a proglacial stream food web

Science.gov (United States)

Fellman, Jason; Hood, Eran; Raymond, Peter A.; Hudson, J.H.; Bozeman, Maura; Arimitsu, Mayumi L.

2015-01-01

We used natural abundance δ13C, δ15N, and Δ14C to compare trophic linkages between potential carbon sources (leaf litter, epilithic biofilm, and particulate organic matter) and consumers (aquatic macroinvertebrates and fish) in a nonglacial stream and two reaches of the heavily glaciated Herbert River. We tested the hypothesis that proglacial stream food webs are sustained by organic carbon released from glacial ecosystems. Carbon sources and consumers in the nonglacial stream had carbon isotope values that ranged from -30‰ to -25‰ for δ13C and from -14‰ to 53‰ for Δ14C reflecting a food web sustained mainly on contemporary primary production. In contrast, biofilm in the two glacial stream sites was highly Δ14C-depleted (-215‰ to 175‰) relative to the nonglacial stream consistent with the assimilation of ancient glacier organic carbon. IsoSource modeling showed that in upper Herbert River, macroinvertebrates (Δ14C = -171‰ to 22‰) and juvenile salmonids (Δ14C = −102‰ to 17‰) reflected a feeding history of both biofilm (~ 56%) and leaf litter (~ 40%). We estimate that in upper Herbert River on average 36% of the carbon incorporated into consumer biomass is derived from the glacier ecosystem. Thus, 14C-depleted glacial organic carbon was likely transferred to higher trophic levels through a feeding history of bacterial uptake of dissolved organic carbon and subsequent consumption of 14C-depleted biofilm by invertebrates and ultimately fish. Our findings show that the metazoan food web is sustained in part by glacial organic carbon such that future changes in glacial runoff could influence the stability and trophic structure of proglacial aquatic ecosystems.

Net ecosystem production and organic carbon balance of U.S. East Coast estuaries: A synthesis approach

Science.gov (United States)

Herrmann, Maria; Najjar, Raymond G.; Kemp, W. Michael; Alexander, Richard B.; Boyer, Elizabeth W.; Cai, Wei-Jun; Griffith, Peter C.; Kroeger, Kevin D.; McCallister, S. Leigh; Smith, Richard A.

2015-01-01

Net ecosystem production (NEP) and the overall organic carbon budget for the estuaries along the East Coast of the United States are estimated. We focus on the open estuarine waters, excluding the fringing wetlands. We developed empirical models relating NEP to loading ratios of dissolved inorganic nitrogen to total organic carbon, and carbon burial in the sediment to estuarine water residence time and total nitrogen input across the landward boundary. Output from a data-constrained water quality model was used to estimate inputs of total nitrogen and organic carbon to the estuaries across the landward boundary, including fluvial and tidal-wetland sources. Organic carbon export from the estuaries to the continental shelf was computed by difference, assuming steady state. Uncertainties in the budget were estimated by allowing uncertainties in the supporting model relations. Collectively, U.S. East Coast estuaries are net heterotrophic, with the area-integrated NEP of −1.5 (−2.8, −1.0) Tg C yr−1 (best estimate and 95% confidence interval) and area-normalized NEP of −3.2 (−6.1, −2.3) mol C m−2 yr−1. East Coast estuaries serve as a source of organic carbon to the shelf, exporting 3.4 (2.0, 4.3) Tg C yr−1 or 7.6 (4.4, 9.5) mol C m−2 yr−1. Organic carbon inputs from fluvial and tidal-wetland sources for the region are estimated at 5.4 (4.6, 6.5) Tg C yr−1 or 12 (10, 14) mol C m−2 yr−1 and carbon burial in the open estuarine waters at 0.50 (0.33, 0.78) Tg C yr−1 or 1.1 (0.73, 1.7) mol C m−2 yr−1. Our results highlight the importance of estuarine systems in the overall coastal budget of organic carbon, suggesting that in the aggregate, U.S. East Coast estuaries assimilate (via respiration and burial) ~40% of organic carbon inputs from fluvial and tidal-wetland sources and allow ~60% to be exported to the shelf.

Organic carbon source and C/N ratio affect inorganic nitrogen profile in the biofloc-based culture media of Pacific white shrimp (Litopenaeus vannamei

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Muhammad Hanif Azhar

2016-03-01

Full Text Available Organic carbon source and C/N ratio play an important role in aquaculture system with biofloc technology application. Nitrogen control by adding carbohydrates to the water to stimulate heterotrophic bacterial growth by converting nitrogen into bacterial biomass. The study investigated the effect molasses, tapioca, tapioca by product and rice bran as carbon sources in a biofloc media at three different C/N ratios i.e. 10, 15, and 20 on total ammonia reduction in biofloc media. Five liters of biofloc media in a conical tank was prepared for each replicate, which consisted of 500 mL of biofloc suspension collected from a shrimp culture unit with biofloc technology application and 4.5 L seawater. Pacific white shrimp culture was performed in 40L glass aquaria at a shrimp density of 30/aquarium. There was a significant interaction between carbon source and the C/N ratio applied (P<0.05. The use of molasses resulted in the highest reduction rate irrespective to the C/N ratio. Keywords: molasses, tapioca, tapioca by product, rice bran, biofloc, total ammonia nitrogen

Nanophase Carbonates on Mars: Does Evolved Gas Analysis of Nanophase Carbonates Reveal a Large Organic Carbon Budget in Near-surface Martian Materials?

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Archer, P. D., Jr.; Ming, D. W.; Sutter, B.; Niles, P. B.; Eigenbrode, J. L.

2015-12-01

Evolved Gas Analysis (EGA), which involves heating a sample and monitoring the gases released, has been performed on Mars by the Viking gas chromatography/mass spectrometry instruments, the Thermal and Evolved Gas Analyzer (TEGA) on the Phoenix lander, and the Sample Analysis at Mars (SAM) instrument on the Mars Science Laboratory. All of these instruments detected CO2 released during sample analysis at abundances of ~0.1 to 5 wt% assuming a carbonate source. The source of the CO2 can be constrained by evaluating the temperature of the gas release, a capability of both the TEGA and SAM instruments. The samples analyzed by SAM show that the majority of the CO2is released below 400 °C, much lower than traditional carbonate decomposition temperatures which can be as low as 400 °C for some siderites, with magnesites and calcites decomposing at even higher temperatures. In addition to mineralogy, decomposition temperature can depend on particle size (among other factors). If carbonates formed on Mars under low temperature and relative humidity conditions, the resulting small particle size (nanophase) carbonates could have low decomposition temperatures. We have found that calcite can be synthesized by exposing CaO to water vapor and CO2 and that the resulting mineral has an EGA peak of ~550 °C for CO2, which is about 200 °C lower than for other calcites. Work is ongoing to produce Fe and Mg-bearing carbonates using the same process. Current results suggest that nanophase calcium carbonates cannot explain the CO2 released from martian samples. If the decomposition temperatures of Mg and Fe-bearing nanophase carbonates are not significantly lower than 400 °C, other candidate sources include oxalates and carboxylated organic molecules. If present, the abundance of organic carbon in these samples could be > 0.1 wt % (1000s of ppm), a signficant departure from the paradigm of the organic-poor Mars based on Viking results.

Effect of nutrient enrichment on the source and composition of sediment organic carbon in tropical seagrass beds in the South China Sea

International Nuclear Information System (INIS)

Liu, Songlin; Jiang, Zhijian; Zhang, Jingping; Wu, Yunchao; Lian, Zhonglian; Huang, Xiaoping

2016-01-01

To assess the effect of nutrient enrichment on the source and composition of sediment organic carbon (SOC) beneath Thalassia hemprichii and Enhalus acoroides in tropical seagrass beds, Xincun Bay, South China Sea, intertidal sediment, primary producers, and seawater samples were collected. No significant differences on sediment δ 13 C, SOC, and microbial biomass carbon (MBC) were observed between T. hemprichii and E. acoroides. SOC was mainly of autochthonous origin, while the contribution of seagrass to SOC was less than that of suspended particulate organic matter, macroalgae and epiphytes. High nutrient concentrations contributed substantially to SOC of seagrass, macroalgae, and epiphytes. The SOC, MBC, and MBC/SOC ratio in the nearest transect to fish farming were the highest. This suggested a more labile composition of SOC and shorter turnover times in higher nutrient regions. Therefore, the research indicates that nutrient enrichment could enhance plant-derived contributions to SOC and microbial use efficiency. - Highlights: • Response of sources and composition of SOC to nutrient enrichment was observed. • Similar SOC sources and composition were observed in the two seagrass communities. • Nutrient enrichment enhanced seagrass and macroalgae and epiphytes contribution to SOC. • High nutrient concentration stimulated the MBC and the MBC/SOC ratio.

Influencing factors on δ(13C) of organic matter and carbonate in labke sediments on songnen plain

International Nuclear Information System (INIS)

Ou Wenjia; Zhang Chengjun

2009-01-01

Carbon isotopic compositions of organic matter and carbonate in surface sediments from lakes in Songnen Plain, northeast of China, were carried out.n-alkanes carbon distribution characteristics of the organic matter in lake sediments were also analyzed to identify the source of organic matter and sedimentary environment in these lakes. With the limnological characteristics of water and sediment, the influencing factors on isotopic composition in sedimentary organic matter and carbonate were discussed. The results showed that types of organic matter affected the carbon isotopic composition. 13 C of carbonate depleted by input of biologic organic matter and enriched by input of oil pollution. (authors)

UTILIZATION OF PINEAPPLE WASTE AS CARBON SOURCE

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Abdullah Moch Busairi

2012-02-01

Full Text Available The liquid pineapple waste contains mainly sucrose, glucose, fructose and other nutrients. It therefore can potentially be used as carbon source for organic acid fermentation.  The objective of this work is to evaluate the use of pineapple waste as substrate for lactic acid fermentation under variables of aerobic, anaerobic condition and pH controlling. Initial results showed that the liquid pineapple waste can be used as carbon source for lactic acid fermentation using Lactobacillus delbrueckii. In the anaerobic condition growth of bacteria and lactic acid production better than aerobic condition. In the anaerobic condition and the controlled pH  the production of lactic acid are found to be 54.79 g/l  (78.27% yield at  40oC, pH 6, 50 rpm and 70 g/l sugar concentration.  In contrast, only 13.87g/l lactic acid produced if the fermentation pH was not controlled even though the fermentation parameters were kept at the same conditions

Process based modelling of soil organic carbon redistribution on landscape scale

Science.gov (United States)

Schindewolf, Marcus; Seher, Wiebke; Amorim, Amorim S. S.; Maeso, Daniel L.; Jürgen, Schmidt

2014-05-01

Recent studies have pointed out the great importance of erosion processes in global carbon cycling. Continuous erosion leads to a massive loss of top soils including the loss of organic carbon accumulated over long time in the soil humus fraction. Lal (2003) estimates that 20% of the organic carbon eroded with top soils is emitted into atmosphere, due to aggregate breakdown and carbon mineralization during transport by surface runoff. Furthermore soil erosion causes a progressive decrease of natural soil fertility, since cation exchange capacity is associated with organic colloids. As a consequence the ability of soils to accumulate organic carbon is reduced proportionately to the drop in soil productivity. The colluvial organic carbon might be protected from further degradation depending on the depth of the colluvial cover and local decomposing conditions. Some colluvial sites can act as long-term sinks for organic carbon. The erosional transport of organic carbon may have an effect on the global carbon budget, however, it is uncertain, whether erosion is a sink or a source for carbon in the atmosphere. Another part of eroded soils and organic carbon will enter surface water bodies and might be transported over long distances. These sediments might be deposited in the riparian zones of river networks. Erosional losses of organic carbon will not pass over into atmosphere for the most part. But soil erosion limits substantially the potential of soils to sequester atmospheric CO2 by generating humus. The present study refers to lateral carbon flux modelling on landscape scale using the process based EROSION 3D soil loss simulation model, using existing parameter values. The selective nature of soil erosion results in a preferentially 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. For this reason it is essential that EROSION 3D provides the

Nitrogen reduction pathways in estuarine sediments: Influences of organic carbon and sulfide

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Plummer, Patrick; Tobias, Craig; Cady, David

2015-10-01

Potential rates of sediment denitrification, anaerobic ammonium oxidation (anammox), and dissimilatory nitrate reduction to ammonium (DNRA) were mapped across the entire Niantic River Estuary, CT, USA, at 100-200 m scale resolution consisting of 60 stations. On the estuary scale, denitrification accounted for ~ 90% of the nitrogen reduction, followed by DNRA and anammox. However, the relative importance of these reactions to each other was not evenly distributed through the estuary. A Nitrogen Retention Index (NIRI) was calculated from the rate data (DNRA/(denitrification + anammox)) as a metric to assess the relative amounts of reactive nitrogen being recycled versus retained in the sediments following reduction. The distribution of rates and accompanying sediment geochemical analytes suggested variable controls on specific reactions, and on the NIRI, depending on position in the estuary and that these controls were linked to organic carbon abundance, organic carbon source, and pore water sulfide concentration. The relationship between NIRI and organic carbon abundance was dependent on organic carbon source. Sulfide proved the single best predictor of NIRI, accounting for 44% of its observed variance throughout the whole estuary. We suggest that as a single metric, sulfide may have utility as a proxy for gauging the distribution of denitrification, anammox, and DNRA.

Assessment of self-organizing maps to analyze sole-carbon source utilization profiles.

Science.gov (United States)

Leflaive, Joséphine; Céréghino, Régis; Danger, Michaël; Lacroix, Gérard; Ten-Hage, Loïc

2005-07-01

The use of community-level physiological profiles obtained with Biolog microplates is widely employed to consider the functional diversity of bacterial communities. Biolog produces a great amount of data which analysis has been the subject of many studies. In most cases, after some transformations, these data were investigated with classical multivariate analyses. Here we provided an alternative to this method, that is the use of an artificial intelligence technique, the Self-Organizing Maps (SOM, unsupervised neural network). We used data from a microcosm study of algae-associated bacterial communities placed in various nutritive conditions. Analyses were carried out on the net absorbances at two incubation times for each substrates and on the chemical guild categorization of the total bacterial activity. Compared to Principal Components Analysis and cluster analysis, SOM appeared as a valuable tool for community classification, and to establish clear relationships between clusters of bacterial communities and sole-carbon sources utilization. Specifically, SOM offered a clear bidimensional projection of a relatively large volume of data and were easier to interpret than plots commonly obtained with multivariate analyses. They would be recommended to pattern the temporal evolution of communities' functional diversity.

The EC CAST project (carbon-14 source term)

International Nuclear Information System (INIS)

Williams, S. J.

2015-01-01

Carbon-14 is a key radionuclide in the assessment of the safety of underground geological disposal facilities for radioactive wastes. It is possible for carbon-14 to be released from waste packages in a variety of chemical forms, both organic and inorganic, and as dissolved or gaseous species The EC CAST (CArbon-14 Source Term) project aims to develop understanding of the generation and release of carbon-14 from radioactive waste materials under conditions relevant to packaging and disposal. It focuses on the release of carbon-14 from irradiated metals (steels and zirconium alloys), from irradiated graphite and from spent ion-exchange resins. The CAST consortium brings together 33 partners. CAST commenced in October 2013 and this paper describes progress to March 2015. The main activities during this period were reviews of the current status of knowledge, the identification and acquisition of suitable samples and the design of experiments and analytical procedures. (authors)

Using Novel Laboratory Incubations and Field Experiments to Identify the Source and Fate of Reactive Organic Carbon in an Arsenic-contaminated Aquifer System

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Stahl, M.; Tarek, M. H.; Badruzzaman, B.; Harvey, C. F.

2017-12-01

Characterizing the sources and fate of organic matter (OM) within aquifer systems is key to our understanding of both the broader global carbon cycle as well as the quality of our groundwater resources. The linkage between the subsurface carbon cycle and groundwater quality is perhaps nowhere more apparent than in the aquifer systems of South and Southeast Asia, where the contamination of groundwater with geogenic arsenic (As) is widespread and threatens the health of millions of individuals. OM fuels the biogeochemical processes driving As mobilization within these aquifers, however the source (i.e., modern surface-derived or aged sedimentary OM) of the reactive OM is widely debated. To characterize the sources of OM driving aquifer redox processes we tracked DIC and DOC concentrations and isotopes (stable and radiocarbon) along groundwater flow-paths and beneath an instrumented study pond at a field site in Bangladesh. We also conducted a set of novel groundwater incubation experiments, where we carbon-dated the DOC at the start and end of a experiment in order to determine the age of the OM that was mineralized. Our carbon/isotope balance reveals that aquifer recharge introduces a large quantity of young (i.e. near modern) OM that is efficiently mineralized within the upper few meters of the aquifer, effectively limiting this pool of reactive surface-sourced OM from being transported deeper into the aquifer where significant As mobilization takes place. The OM mineralized past the upper few meters is an aged, sedimentary source. Consistent with our field data, our incubation experiments show that past the upper few meters of the aquifer the reactive DOC is significantly older than the bulk DOC and has an age consistent with sedimentary OM. Combining our novel set of incubation experiments and a carbon/isotope balance along groundwater flow-paths and beneath our study pond we have identified the sources of reactive OM across different aquifer depths in a

Distribution and sources of particulate organic matter in the Indian monsoonal estuaries during monsoon

Digital Repository Service at National Institute of Oceanography (India)

Sarma, V.V.S.S.; Krishna, M.S.; Prasad, V.R.; Kumar, B.S.K.; Naidu, S.A.; Rao, G.D.; Viswanadham, R.; Sridevi, T.; Kumar, P.P.; Reddy, N.P.C.

The distribution and sources of particulate organic carbon (POC) and nitrogen (PN) in 27 Indian estuaries were examined during the monsoon using the content and isotopic composition of carbon and nitrogen. Higher phytoplankton biomass was noticed...

The role of hydrology in annual organic carbon loads and terrestrial organic matter export from a midwestern agricultural watershed

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Dalzell, Brent J.; Filley, Timothy R.; Harbor, Jon M.

2007-03-01

Defining the control that hydrology exerts on organic carbon (OC) export at the watershed scale is important for understanding how the source and quantity of OC in streams and rivers is influenced by climate change or by landscape drainage. To this end, molecular (lignin phenol), stable carbon isotope, and dissolved organic carbon (DOC) data were collected over a range of flow conditions to examine the influence of hydrology on annual OC export from an 850 km 2 Midwestern United States agricultural watershed located in west central Indiana. In years 2002 and 2003, modeled annual DOC loads were 19.5 and 14.1 kg ha -1yr -1, while 71% and 85%, respectively, of the total annual OC was exported in flow events occurring during less than 20% of that time. These results highlight the importance of short-duration, high-discharge events (common in smaller watersheds) in controlling annual OC export. Based on reported increases in annual stream discharge coupled with current estimates of DOC export, annual DOC loads in this watershed may have increased by up to 40% over the past 50 years. Molecular (lignin phenol) characterization of quantity and relative degradation state of terrestrial OC shows as much temporal variability of lignin parameters (in high molecular weight dissolved organic carbon) in this one watershed as that demonstrated in previously published studies of dissolved organic matter in the Mississippi and Amazon Rivers. These results suggest that hydrologic variability is at least as important in determining the nature and extent of OC export as geographic variability. Moreover, molecular and bulk stable carbon isotope data from high molecular weight dissolved organic carbon and colloidal organic carbon showed that increased stream flow from the study watershed was responsible for increased export of agriculturally derived OC. When considered in the context of results from other studies that show the importance of flood events and in-stream processing of

Wintertime aerosol chemical composition and source apportionment of the organic fraction in the metropolitan area of Paris

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M. Crippa

2013-01-01

Full Text Available The effect of a post-industrial megacity on local and regional air quality was assessed via a month-long field measurement campaign in the Paris metropolitan area during winter 2010. Here we present source apportionment results from three aerosol mass spectrometers and two aethalometers deployed at three measurement stations within the Paris region. Submicron aerosol composition is dominated by the organic fraction (30–36% and nitrate (28–29%, with lower contributions from sulfate (14–16%, ammonium (12–14% and black carbon (7–13%.

Organic source apportionment was performed using positive matrix factorization, resulting in a set of organic factors corresponding both to primary emission sources and secondary production. The dominant primary sources are traffic (11–15% of organic mass, biomass burning (13–15% and cooking (up to 35% during meal hours. Secondary organic aerosol contributes more than 50% to the total organic mass and includes a highly oxidized factor from indeterminate and/or diverse sources and a less oxidized factor related to wood burning emissions. Black carbon was apportioned to traffic and wood burning sources using a model based on wavelength-dependent light absorption of these two combustion sources. The time series of organic and black carbon factors from related sources were strongly correlated. The similarities in aerosol composition, total mass and temporal variation between the three sites suggest that particulate pollution in Paris is dominated by regional factors, and that the emissions from Paris itself have a relatively low impact on its surroundings.

Source apportionment of PM10 mass and particulate carbon in the Kathmandu Valley, Nepal

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Kim, Bong Mann; Park, Jin-Soo; Kim, Sang-Woo; Kim, Hyunjae; Jeon, Haeun; Cho, Chaeyoon; Kim, Ji-Hyoung; Hong, Seungkyu; Rupakheti, Maheswar; Panday, Arnico K.; Park, Rokjin J.; Hong, Jihyung; Yoon, Soon-Chang

2015-12-01

The Kathmandu Valley in Nepal is a bowl-shaped urban basin in the Himalayan foothills with a serious problem of fine particulate air pollution that impacts local health and impairs visibility. Particulate carbon concentrations have reached severe levels that threaten the health of 3.5 million local residents. Moreover, snow and ice on the Himalayan mountains are melting as a result of additional warming due to particulate carbon, especially high black carbon concentrations. To date, the sources of the Valley's particulate carbon and the impacts of different sources on particulate carbon concentrations are not well understood. Thus, before an effective control strategy can be developed, these particulate carbon sources must be identified and quantified. Our study has found that the four primary sources of particulate carbon in the Kathmandu Valley during winter are brick kilns, motor vehicles, fugitive soil dust, and biomass/garbage burning. Their source contributions are quantified using a recently developed new multivariate receptor model SMP. In contrast to other highly polluted areas such as China, secondary contribution is almost negligible in Kathmandu Valley. Brick kilns (40%), motor vehicles (37%) and biomass/garbage burning (22%) have been identified as the major sources of elemental carbon (black carbon) in the Kathmandu Valley during winter, while motor vehicles (47%), biomass/garbage burning (32%), and soil dust (13%) have been identified as the most important sources of organic carbon. Our research indicates that controlling emissions from motor vehicles, brick kilns, biomass/garbage burning, and soil dust is essential for the mitigation of the particulate carbon that threatens public health, impairs visibility, and influences climate warming within and downwind from the Kathmandu Valley. In addition, this paper suggests several useful particulate carbon mitigation methods that can be applied to Kathmandu Valley and other areas in South Asia with

DEVELOP NEW TOTAL ORGANIC CARBON/SPECIFIC UV ...

Science.gov (United States)

The purpose of this project is to provide a total organic carbon (TOC)/specific ultraviolet absorbance (SUVA) method that will be used by the Office of Ground Water and Drinking Water (OGWDW) to support monitoring requirements of the Stage 2 Disinfectant/Disinfection By-products (D/DBP) Rule. The Stage 2 Rule requires that enhanced water treatment be used if the source water is high in aquatic organic matter prior to the application of a disinfectant. Disinfectants (chlorine, ozone, etc.) are used in the production of drinking water in order to reduce the risk of microbial disease. These disinfectants react with the organic material that is naturally present in the source water to form disinfection by-products (DBPs). Exposure to some of these by-products may pose a long term health risk. The number and nature of DBPs make it impossible to fully characterize all of the by-products formed during the treatment of drinking water and it is more cost effective to reduce formation of DBPs than to remove them from the water after they are formed. Two measurements (TOC and SUVA) are believed to be predictive of the amount of by-products that can be formed during the disinfection of drinking water and are considered to be surrogates for DBP precursors. SUVA is calculated as the ultraviolet absorption at 254nm (UV254) in cm-1 divided by the mg/L dissolved organic carbon (DOC) concentration (measured after filtration of the water through a 0.45um pore-diameter filte

[Harvest of the carbon source in wastewater by the adsorption and desorption of activated sludge].

Science.gov (United States)

Liu, Hong-Bo; Wen, Xiang-Hua; Zhao, Fang; Mei, Yi-Jun

2011-04-01

The carbon source in municipal wastewater was adsorbed by activated sludge and then harvested through the hydrolysis of activated sludge. Results indicated that activated sludge had high absorbing ability towards organic carbon and phosphorus under continuous operation mode, and the average COD and TP absorption rate reached as high as 63% and 76%, respectively. Moreover, about 50% of the soluble carbon source was outside of the sludge cell and could be released under mild hydrolysis condition. Whereas the absorbed amount of nitrogen was relatively low, and the removal rate of ammonia was only 13% . Furthermore, the releases of organic carbon, nitrogen and phosphorus from the sludge absorbing pollutants in the wastewater were studied. By comparing different hydrolysis conditions of normal (pH 7.5, 20 degrees C), heating (pH 7.5, 60 degrees C) and the alkaline heating (pH 11, 60 degrees C), the last one presented the optimum hydrolysis efficiency. Under which, the release rate of COD could reach 320 mg/g after 24 hours, whereas nitrogen and phosphorus just obtained low release rates of 18 mg/g and 2 mg/g, respectively. Results indicate that the carbon source in wastewater could be harvested by the adsorption and desorption of activated sludge, and the concentrations of nitrogen and phosphorus are low and would not influence the reuse of the harvested carbon source.

Constraining the sources and cycling of dissolved organic carbon in a large oligotrophic lake using radiocarbon analyses

Science.gov (United States)

Zigah, Prosper K.; Minor, Elizabeth C.; McNichol, Ann P.; Xu, Li; Werne, Josef P.

2017-07-01

We measured the concentrations and isotopic compositions of solid phase extracted (SPE) dissolved organic carbon (DOC) and high molecular weight (HMW) DOC and their constituent organic components in order to better constrain the sources and cycling of DOC in a large oligotrophic lacustrine system (Lake Superior, North America). SPE DOC constituted a significant proportion (41-71%) of the lake DOC relative to HMW DOC (10-13%). Substantial contribution of 14C-depleted components to both SPE DOC (Δ14C = 25-43‰) and HMW DOC (Δ14C = 22-32‰) was evident during spring mixing, and depressed their radiocarbon values relative to the lake dissolved inorganic carbon (DIC; Δ14C ∼ 59‰). There was preferential removal of 14C-depleted (older) and thermally recalcitrant components from HMW DOC and SPE DOC in the summer. Contemporary photoautotrophic addition to HMW DOC was observed during summer stratification in contrast to SPE DOC, which decreased in concentration during stratification. Serial thermal oxidation radiocarbon analysis revealed a diversity of sources (both contemporary and older) within the SPE DOC, and also showed distinct components within the HMW DOC. The thermally labile components of HMW DOC were 14C-enriched and are attributed to heteropolysaccharides (HPS), peptides/amide and amino sugars (AMS) relative to the thermally recalcitrant components reflecting the presence of older material, perhaps carboxylic-rich alicyclic molecules (CRAM). The solvent extractable lipid-like fraction of HMW DOC was very 14C-depleted (as old as 1270-2320 14C years) relative to the carbohydrate-like and protein-like substances isolated by acid hydrolysis of HMW DOC. Our data constrain relative influences of contemporary DOC and old DOC, and DOC cycling in a modern freshwater ecosystem.

Could a secular increase in organic burial explain the rise of oxygen? Insights from a geological carbon cycle model constrained by the carbon isotope record

Science.gov (United States)

Krissansen-Totton, J.; Kipp, M.; Catling, D. C.

2017-12-01

The stable isotopes of carbon in marine sedimentary rock provide a window into the evolution of the Earth system. Conventionally, a relatively constant carbon isotope ratio in marine sedimentary rocks has been interpreted as implying constant organic carbon burial relative to total carbon burial. Because organic carbon burial corresponds to net oxygen production from photosynthesis, it follows that secular changes in the oxygen source flux cannot explain the dramatic rise of oxygen over Earth history. Instead, secular declines in oxygen sink fluxes are often invoked as causes for the rise of oxygen. However, constant fractional organic burial is difficult to reconcile with tentative evidence for low phosphate concentrations in the Archean ocean, which would imply lower marine productivity and—all else being equal—less organic carbon burial than today. The conventional interpretation of the carbon isotope record rests on the untested assumption that the isotopic ratio of carbon inputs into the ocean reflect mantle isotopic values throughout Earth history. In practice, differing rates of carbonate and organic weathering will allow for changes in isotopic inputs, as suggested by [1] and [2]. However, these inputs can not vary freely because large changes in isotopic inputs would induce secular trends in carbon reservoirs, which are not observed in the isotope record. We apply a geological carbon cycle model to all Earth history, tracking carbon isotopes in crustal, mantle, and ocean reservoirs. Our model is constrained by the carbon isotope record such that we can determine the extent to which large changes in organic burial are permitted. We find both constant organic burial and 3-5 fold increases in organic burial since 4.0 Ga can be reconciled with the carbon isotope record. Changes in the oxygen source flux thus need to be reconsidered as a possible contributor to Earth's oxygenation. [1] L. A. Derry, Organic carbon cycling and the lithosphere, in Treatise on

Quantifying Sources and Fluxes of Aquatic Carbon in U.S. Streams and Reservoirs Using Spatially Referenced Regression Models

Science.gov (United States)

Boyer, E. W.; Smith, R. A.; Alexander, R. B.; Schwarz, G. E.

2004-12-01

Organic carbon (OC) is a critical water quality characteristic in riverine systems that is an important component of the aquatic carbon cycle and energy balance. Examples of processes controlled by OC interactions are complexation of trace metals; enhancement of the solubility of hydrophobic organic contaminants; formation of trihalomethanes in drinking water; and absorption of visible and UV radiation. Organic carbon also can have indirect effects on water quality by influencing internal processes of aquatic ecosystems (e.g. photosynthesis and autotrophic and heterotrophic activity). The importance of organic matter dynamics on water quality has been recognized, but challenges remain in quantitatively addressing OC processes over broad spatial scales in a hydrological context. In this study, we apply spatially referenced watershed models (SPARROW) to statistically estimate long-term mean-annual rates of dissolved- and total- organic carbon export in streams and reservoirs across the conterminous United States. We make use of a GIS framework for the analysis, describing sources, transport, and transformations of organic matter from spatial databases providing characterizations of climate, land use, primary productivity, topography, soils, and geology. This approach is useful because it illustrates spatial patterns of organic carbon fluxes in streamflow, highlighting hot spots (e.g., organic-rich environments in the southeastern coastal plain). Further, our simulations provide estimates of the relative contributions to streams from allochthonous and autochthonous sources. We quantify surface water fluxes of OC with estimates of uncertainty in relation to the overall US carbon budget; our simulations highlight that aquatic sources and sinks of OC may be a more significant component of regional carbon cycling than was previously thought. Further, we are using our simulations to explore the potential role of climate and other changes in the terrestrial environment on

Deposition and Burial Efficiency of Terrestrial Organic Carbon Exported from Small Mountainous Rivers to the Continental Margin, Southwest of Taiwan

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Hsu, F.; Lin, S.; Wang, C.; Huh, C.

2007-12-01

Terrestrial organic carbon exported from small mountainous river to the continental margin may play an important role in global carbon cycle and it?|s biogeochemical process. A huge amount of suspended materials from small rivers in southwestern Taiwan (104 million tons per year) could serve as major carbon source to the adjacent ocean. However, little is know concerning fate of this terrigenous organic carbon. The purpose of this study is to calculate flux of terrigenous organic carbon deposited in the continental margin, offshore southwestern Taiwan through investigating spatial variation of organic carbon content, organic carbon isotopic compositions, organic carbon deposition rate and burial efficiency. Results show that organic carbon compositions in sediment are strongly influenced by terrestrial material exported from small rivers in the region, Kaoping River, Tseng-wen River and Er-jan Rver. In addition, a major part of the terrestrial materials exported from the Kaoping River may bypass shelf region and transport directly into the deep sea (South China Sea) through the Kaoping Canyon. Organic carbon isotopic compositions with lighter carbon isotopic values are found near the Kaoping River and Tseng-wen River mouth and rapidly change from heavier to lighter values through shelf to slope. Patches of lighter organic carbon isotopic compositions with high organic carbon content are also found in areas west of Kaoping River mouth, near the Kaoshiung city. Furthermore, terrigenous organic carbons with lighter isotopic values are found in the Kaoping canyon. A total of 0.028 Mt/yr of terrestrial organic carbon was found in the study area, which represented only about 10 percent of all terrestrial organic carbon deposited in the study area. Majority (~90 percent) of the organic carbon exported from the Kaoping River maybe directly transported into the deep sea (South China Sea) and become a major source of organic carbon in the deep sea.

Understanding the carbon cycle in a Late Quaternary-age limestone aquifer system using radiocarbon of dissolved inorganic and organic carbon

Science.gov (United States)

Bryan, Eliza; Meredith, Karina T.; Baker, Andy; Andersen, Martin S.; Post, Vincent E. A.

2017-04-01

Estimating groundwater residence time is critical for our understanding of hydrogeological systems, for groundwater resource assessments and for the sustainable management of groundwater resources. Due to its capacity to date groundwater up to 30 thousand years old, as well as the ubiquitous nature of dissolved carbon (as organic and inorganic forms) in groundwater, 14C is the most widely used radiogenic dating technique in regional aquifers. However, the geochemistry of carbon in groundwater systems includes interaction with the atmosphere, biosphere and geosphere, which results in multiple sources and sinks of carbon that vary in time and space. Identifying these sources of carbon and processes relating to its release or removal is important for understanding the evolution of the groundwater and essential for residence time calculations. This study investigates both the inorganic and organic facets of the carbon cycle in groundwaters throughout a freshwater lens and mixing zone of a carbonate island aquifer and identifies the sources of carbon that contribute to the groundwater system. Groundwater samples were collected from shallow (5-20 m) groundwater wells on a small carbonate Island in Western Australia in September 2014 and analysed for major and minor ions, stable water isotopes (SWIs: δ18O, δ2H), 3H, 14C and 13C carbon isotope values of both DIC and DOC, and 3H. The composition of groundwater DOC was investigated by Liquid Chromatography-Organic Carbon Detection (LC-OCD) analysis. The presence of 3H (0.12 to 1.35 TU) in most samples indicates that groundwaters on the Island are modern, however the measured 14CDIC values (8.4 to 97.2 pmc) suggest that most samples are significantly older due to carbonate dissolution and recrystallisation reactions that are identified and quantified in this work. 14CDOC values (46.6 to 105.6 pMC) were higher than 14CDIC values and were well correlated with 3H values, however deeper groundwaters had lower 14CDOC values than

Distinguishing Terrestrial Organic Carbon in Marginal Sediments of East China Sea and Northern South China Sea

Science.gov (United States)

Kandasamy, Selvaraj; Lin, Baozhi; Wang, Huawei; Liu, Qianqian; Liu, Zhifei; Lou, Jiann-Yuh; Chen, Chen-Tung Arthur; Mayer, Lawrence M.

2016-04-01

Knowledge about the sources, transport pathways and behavior of terrestrial organic carbon in continental margins adjoining to large rivers has improved in recent decades, but uncertainties and complications still exist with human-influenced coastal regions in densely populated wet tropics and subtropics. In these regions, the monsoon and other episodic weather events exert strong climatic control on mineral and particulate organic matter delivery to the marginal seas. Here we investigate elemental (TOC, TN and bromine-Br) and stable carbon isotopic (δ13C) compositions of organic matter (OM) in surface sediments and short cores collected from active (SW Taiwan) and passive margin (East China Sea) settings to understand the sources of OM that buried in these settings. We used sedimentary bromine to total organic carbon (Br/TOC) ratios to apportion terrigenous from marine organic matter, and find that Br/TOC may serve as an additional, reliable proxy for sedimentary provenance in both settings. Variations in Br/TOC are consistent with other provenance indicators in responding to short-lived terrigenous inputs. Because diagenetic alteration of Br is insignificant on shorter time scales, applying Br/TOC ratios as a proxy to identify organic matter source along with carbon isotope mixing models may provide additional constraints on the quantity and transformation of terrigenous organics in continental margins. We apply this combination of approaches to land-derived organic matter in different depositional environments of East Asian marginal seas.

Water soluble organic aerosols in the Colorado Rocky Mountains, USA: composition, sources and optical properties

OpenAIRE

Xie, Mingjie; Mladenov, Natalie; Williams, Mark W.; Neff, Jason C.; Wasswa, Joseph; Hannigan, Michael P.

2016-01-01

Atmospheric aerosols have been shown to be an important input of organic carbon and nutrients to alpine watersheds and influence biogeochemical processes in these remote settings. For many remote, high elevation watersheds, direct evidence of the sources of water soluble organic aerosols and their chemical and optical characteristics is lacking. Here, we show that the concentration of water soluble organic carbon (WSOC) in the total suspended particulate (TSP) load at a high elevation site in...

Functional group composition of ambient and source organic aerosols determined by tandem mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Dron, J.; El Haddad, I.; Temime-Roussel, B.; Wortham, H.; Marchand, N. [Univ Aix Marseille, CNRS, Lab Chim Provence, Equipe Instrumentat and React Atmospher, UMR 6264, F-13331 Marseille 3 (France); Jaffrezo, J.L. [Univ Grenoble 1, CNRS, UMR 5183, Lab Glaciol and Geophys Environm, F-38402 St Martin Dheres (France)

2010-07-01

The functional group composition of various organic aerosols (OA) is investigated using a recently developed analytical approach based on atmospheric pressure chemical ionisation-tandem mass spectrometry (APCIMS/MS). The determinations of three functional groups contents are performed quantitatively by neutral loss (carboxylic and carbonyl groups, R-COOH and R-CO-R' respectively) and precursor ion (nitro groups, R-NO{sub 2}) scanning modes of a tandem mass spectrometer. Major organic aerosol sources are studied: vehicular emission and wood combustion for primary aerosol sources; and a secondary organic aerosol (SOA) produced through photooxidation of o-xylene. The results reveal significant differences in the functional group contents of these source aerosols. The laboratory generated SOA is dominated by carbonyls while carboxylics are preponderate in the wood combustion particles. On the other hand, vehicular emissions are characterised by a strong nitro content. The total amount of the three functional groups accounts for 1.7% (vehicular) to 13.5% (o-xylene photooxidation) of the organic carbon. Diagnostic functional group ratios are then used to tentatively discriminate sources of particles collected in an urban background environment located in an Alpine valley (Chamonix, France) during a strong winter pollution event. The three functional groups under study account for a total functionalization rate of 2.2 to 3.8% of the organic carbon in this ambient aerosol, which is also dominated by carboxylic moieties. In this particular case study of a deep alpine valley during winter, we show that the nitro- and carbonyl-to-carboxylic diagnostic ratios can be a useful tool to discriminate sources. In these conditions, the total OA concentrations are highly dominated by wood combustion OA. This result is confirmed by an organic markers source apportionment approach which assess a wood burning organic carbon contribution of about 60%. Finally, examples of functional

Functional group composition of ambient and source organic aerosols determined by tandem mass spectrometry

Directory of Open Access Journals (Sweden)

J. Dron

2010-08-01

Full Text Available The functional group composition of various organic aerosols (OA is investigated using a recently developed analytical approach based on atmospheric pressure chemical ionisation-tandem mass spectrometry (APCI-MS/MS. The determinations of three functional groups contents are performed quantitatively by neutral loss (carboxylic and carbonyl groups, R-COOH and R-CO-R´ respectively and precursor ion (nitro groups, R-NO₂ scanning modes of a tandem mass spectrometer. Major organic aerosol sources are studied: vehicular emission and wood combustion for primary aerosol sources; and a secondary organic aerosol (SOA produced through photooxidation of o-xylene. The results reveal significant differences in the functional group contents of these source aerosols. The laboratory generated SOA is dominated by carbonyls while carboxylics are preponderate in the wood combustion particles. On the other hand, vehicular emissions are characterised by a strong nitro content. The total amount of the three functional groups accounts for 1.7% (vehicular to 13.5% (o-xylene photooxidation of the organic carbon. Diagnostic functional group ratios are then used to tentatively discriminate sources of particles collected in an urban background environment located in an Alpine valley (Chamonix, France during a strong winter pollution event. The three functional groups under study account for a total functionalisation rate of 2.2 to 3.8% of the organic carbon in this ambient aerosol, which is also dominated by carboxylic moieties. In this particular case study of a deep alpine valley during winter, we show that the nitro- and carbonyl-to-carboxylic diagnostic ratios can be a useful tool to discriminate sources. In these conditions, the total OA concentrations are highly dominated by wood combustion OA. This result is confirmed by an organic markers source apportionment approach which assess a wood burning organic carbon contribution of about 60

Tracing organic matter sources in a tropical lagoon of the Caribbean Sea

Science.gov (United States)

Alonso-Hernández, Carlos M.; Garcia-Moya, Alejandro; Tolosa, Imma; Diaz-Asencio, Misael; Corcho-Alvarado, Jose Antonio; Morera-Gomez, Yasser; Fanelli, Emanuela

2017-09-01

The natural protected lagoon of Guanaroca, located between Cienfuegos Bay and the Arimao River, Cuba, has been heavily impacted by human-induced environmental changes over the past century. Sources of organic matter in the Guanaroca lagoon and concentrations of radioisotopes (210Pb, 226Ra, 137Cs and 239,240Pu), as tracers of anthropogenic impacts, were investigated in a 78 cm sediment core. Variations in total organic carbon (TOC), total nitrogen (TN), stable isotopic composition (δ13C and δ15N) and ratio of total organic carbon to total nitrogen (C/N) were analysed. On such a basis, environmental changes in the lagoon were revealed. Down core variation patterns of the parameters representing sources of organic matter were predominantly related to the impacts of human activities. Up to the nineteenth century, the principal sources of organic matter to sediments (more than 80%) were a mixing of terrestrial vascular plants ( 48%) and freshwater phytoplankton ( 8%), with minimal contribution from the marine component ( 16%). In the period 1900-1980, due to the strong influence of human activities in the catchment area, the water exchange capacity of the lagoon declined substantially, as indicated by the relatively high proportion of organic matter originated from human activities (58%). Since 1980, as a result of management actions in the protected area, the lagoon has regained gradually its capability to exchange freshwater, showing sources of organic matter similar to the natural conditions recorded previous to 1900, although an indication of human impact (treated sewage contributed for 26% to the organic matter in sediments) was still observed and further management measures would be required.

A mixing-model approach to quantifying sources of organic matter to salt marsh sediments

Science.gov (United States)

Bowles, K. M.; Meile, C. D.

2010-12-01

Salt marshes are highly productive ecosystems, where autochthonous production controls an intricate exchange of carbon and energy among organisms. The major sources of organic carbon to these systems include 1) autochthonous production by vascular plant matter, 2) import of allochthonous plant material, and 3) phytoplankton biomass. Quantifying the relative contribution of organic matter sources to a salt marsh is important for understanding the fate and transformation of organic carbon in these systems, which also impacts the timing and magnitude of carbon export to the coastal ocean. A common approach to quantify organic matter source contributions to mixtures is the use of linear mixing models. To estimate the relative contributions of endmember materials to total organic matter in the sediment, the problem is formulated as a constrained linear least-square problem. However, the type of data that is utilized in such mixing models, the uncertainties in endmember compositions and the temporal dynamics of non-conservative entitites can have varying affects on the results. Making use of a comprehensive data set that encompasses several endmember characteristics - including a yearlong degradation experiment - we study the impact of these factors on estimates of the origin of sedimentary organic carbon in a saltmarsh located in the SE United States. We first evaluate the sensitivity of linear mixing models to the type of data employed by analyzing a series of mixing models that utilize various combinations of parameters (i.e. endmember characteristics such as δ13COC, C/N ratios or lignin content). Next, we assess the importance of using more than the minimum number of parameters required to estimate endmember contributions to the total organic matter pool. Then, we quantify the impact of data uncertainty on the outcome of the analysis using Monte Carlo simulations and accounting for the uncertainty in endmember characteristics. Finally, as biogeochemical processes

Organic carbon in glacial fjords of Chilean Patagonia

Science.gov (United States)

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

Investigation of the Makeup, Source, and Removal Strategies for Total Organic Carbon in the Oxygen Generation System Recirculation Loop

Science.gov (United States)

Bowman, Elizabeth M.; Carpenter, Joyce; Roy, Robert J.; Van Keuren, Steve; Wilson, Mark E.

2015-01-01

Since 2007, the Oxygen Generation System (OGS) on board the International Space Station (ISS) has been producing oxygen for crew respiration via water electrolysis. As water is consumed in the OGS recirculating water loop, make-up water is furnished by the ISS potable water bus. A rise in Total Organic Carbon (TOC) was observed beginning in February, 2011, which continues through the present date. Increasing TOC is of concern because the organic constituents responsible for the TOC were unknown and had not been identified; hence their impacts on the operation of the electrolytic cell stack components and on microorganism growth rates and types are unknown. Identification of the compounds responsible for the TOC increase, their sources, and estimates of their loadings in the OGA as well as possible mitigation strategies are presented.

Organic carbon content of tropical zooplankton

Digital Repository Service at National Institute of Oceanography (India)

Nair, V.R.

In the Zuari and Mandovi estuaries variations in organic carbon of zooplankton are 26.4-38.8 and 24-39.9% of dry weight respectively. Maximum carbon content of estuarine zooplankton is observed in November. Organic carbon in nearshore and oceanic...

Sequestration of organochlorine pesticides in soils of distinct organic carbon content

International Nuclear Information System (INIS)

Zhang Na; Yang Yu; Tao Shu; Liu Yan; Shi Kelu

2011-01-01

In the present study, five soil samples with organic carbon contents ranging from 0.23% to 7.1% and aged with technical dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) for 15 months were incubated in a sealed chamber to investigate the dynamic changes of the OCP residues. The residues in the soils decreased over the incubation period and finally reached a plateau. Regression analysis showed that degradable fractions of OCPs were negatively correlated with soil organic carbon (SOC) except for α-HCH, while no correlation was found between degradation rate and SOC, which demonstrated that SOC content determines the OCP sequestration fraction in soil. Analysis of the ratio of DDT and its primary metabolites showed that, since it depends on differential sequestration among them, magnitude of (p,p'-DDE + p,p'-DDD)/p,p'-DDT is not a reliable criterion for the identification of new DDT sources. - Research highlights: → Soil organic carbon content determines the OCP sequestration fraction in soil. → Magnitude of (p,p'-DDE + p,p'-DDD)/p,p'-DDT is not a reliable criterion for the identification of new DDT sources. → The more hydrophobic compounds have relatively higher sequestration fractions in soils with SOC contents >2%. → DDD may have higher sorption by soil organic matter than DDE. - The effect of soil organic matter on the sequestration of organochlorine pesticides (HCHs and DDTs) in soils was investigated in an innovative microcosm chamber.

Characterization of polar organic compounds and source analysis of fine organic aerosols in Hong Kong

Science.gov (United States)

Li, Yunchun

Organic aerosols, as an important fraction of airborne particulate mass, significantly affect the environment, climate, and human health. Compared with inorganic species, characterization of individual organic compounds is much less complete and comprehensive because they number in thousands or more and are diverse in chemical structures. The source contributions of organic aerosols are far from being well understood because they can be emitted from a variety of sources as well as formed from photochemical reactions of numerous precursors. This thesis work aims to improve the characterization of polar organic compounds and source apportionment analysis of fine organic carbon (OC) in Hong Kong, which consists of two parts: (1) An improved analytical method to determine monocarboxylic acids, dicarboxylic acids, ketocarboxylic acids, and dicarbonyls collected on filter substrates has been established. These oxygenated compounds were determined as their butyl ester or butyl acetal derivatives using gas chromatography-mass spectrometry. The new method made improvements over the original Kawamura method by eliminating the water extraction and evaporation steps. Aerosol materials were directly mixed with the BF 3/BuOH derivatization agent and the extracting solvent hexane. This modification improves recoveries for both the more volatile and the less water-soluble compounds. This improved method was applied to study the abundances and sources of these oxygenated compounds in PM2.5 aerosol samples collected in Hong Kong under different synoptic conditions during 2003-2005. These compounds account for on average 5.2% of OC (range: 1.4%-13.6%) on a carbon basis. Oxalic acid was the most abundant species. Six C2 and C3 oxygenated compounds, namely oxalic, malonic, glyoxylic, pyruvic acids, glyoxal, and methylglyoxal, dominated this suite of oxygenated compounds. More efforts are therefore suggested to focus on these small compounds in understanding the role of oxygenated

Abiotic synthesis of organic compounds from carbon disulfide under hydrothermal conditions.

Science.gov (United States)

Rushdi, Ahmed I; Simoneit, Bernd R T

2005-12-01

Abiotic formation of organic compounds under hydrothermal conditions is of interest to bio, geo-, and cosmochemists. Oceanic sulfur-rich hydrothermal systems have been proposed as settings for the abiotic synthesis of organic compounds. Carbon disulfide is a common component of magmatic and hot spring gases, and is present in marine and terrestrial hydrothermal systems. Thus, its reactivity should be considered as another carbon source in addition to carbon dioxide in reductive aqueous thermosynthesis. We have examined the formation of organic compounds in aqueous solutions of carbon disulfide and oxalic acid at 175 degrees C for 5 and 72 h. The synthesis products from carbon disulfide in acidic aqueous solutions yielded a series of organic sulfur compounds. The major compounds after 5 h of reaction included dimethyl polysulfides (54.5%), methyl perthioacetate (27.6%), dimethyl trithiocarbonate (6.8%), trithianes (2.7%), hexathiepane (1.4%), trithiolanes (0.8%), and trithiacycloheptanes (0.3%). The main compounds after 72 h of reaction consisted of trithiacycloheptanes (39.4%), pentathiepane (11.6%), tetrathiocyclooctanes (11.5%), trithiolanes (10.6%), tetrathianes (4.4%), trithianes (1.2%), dimethyl trisulfide (1.1%), and numerous minor compounds. It is concluded that the abiotic formation of aliphatic straight-chain and cyclic polysulfides is possible under hydrothermal conditions and warrants further studies.

Linking variability in soil solution dissolved organic carbon to climate, soil type, and vegetation type

NARCIS (Netherlands)

Camino-Serrano, Marta; Gielen, Bert; Luyssaert, Sebastiaan; Ciais, Philippe; Vicca, Sara; Guenet, Bertrand; Vos, Bruno De; Cools, Nathalie; Ahrens, Bernhard; Altaf Arain, M.; Borken, Werner; Clarke, Nicholas; Clarkson, Beverley; Cummins, Thomas; Don, Axel; Pannatier, Elisabeth Graf; Laudon, Hjalmar; Moore, Tim; Nieminen, Tiina M.; Nilsson, Mats B.; Peichl, Matthias; Schwendenmann, Luitgard; Siemens, Jan; Janssens, Ivan

2014-01-01

Lateral transport of carbon plays an important role in linking the carbon cycles of terrestrial and aquatic ecosystems. There is, however, a lack of information on the factors controlling one of the main C sources of this lateral flux, i.e., the concentration of dissolved organic carbon (DOC) in

Effect of nutrient enrichment on the source and composition of sediment organic carbon in tropical seagrass beds in the South China Sea.

Science.gov (United States)

Liu, Songlin; Jiang, Zhijian; Zhang, Jingping; Wu, Yunchao; Lian, Zhonglian; Huang, Xiaoping

2016-09-15

To assess the effect of nutrient enrichment on the source and composition of sediment organic carbon (SOC) beneath Thalassia hemprichii and Enhalus acoroides in tropical seagrass beds, Xincun Bay, South China Sea, intertidal sediment, primary producers, and seawater samples were collected. No significant differences on sediment δ(13)C, SOC, and microbial biomass carbon (MBC) were observed between T. hemprichii and E. acoroides. SOC was mainly of autochthonous origin, while the contribution of seagrass to SOC was less than that of suspended particulate organic matter, macroalgae and epiphytes. High nutrient concentrations contributed substantially to SOC of seagrass, macroalgae, and epiphytes. The SOC, MBC, and MBC/SOC ratio in the nearest transect to fish farming were the highest. This suggested a more labile composition of SOC and shorter turnover times in higher nutrient regions. Therefore, the research indicates that nutrient enrichment could enhance plant-derived contributions to SOC and microbial use efficiency. Copyright © 2016 Elsevier Ltd. All rights reserved.

Source attribution of black carbon in Arctic snow.

Science.gov (United States)

Hegg, Dean A; Warren, Stephen G; Grenfell, Thomas C; Doherty, Sarah J; Larson, Timothy V; Clarke, Antony D

2009-06-01

Snow samples obtained at 36 sites in Alaska, Canada, Greenland, Russia, and the Arctic Ocean in early 2007 were analyzed for light-absorbing aerosol concentration together with a suite of associated chemical species. The light absorption data, interpreted as black carbon concentrations, and other chemical data were input into the EPA PMF 1.1 receptor model to explore the sources for black carbon in the snow. The analysis found four factors or sources: two distinct biomass burning sources, a pollution source, and a marine source. The first three of these were responsible for essentially all of the black carbon, with the two biomass sources (encompassing both open and closed combustion) together accounting for >90% of the black carbon.

Characterization of Black and Brown Carbon Concentrations and Sources during winter in Beijing

Science.gov (United States)

Yan, Caiqing; Liu, Yue; Hansen, Anthony D. A.; Močnik, Griša; Zheng, Mei

2017-04-01

Carbonaceous aerosols, including black carbon (BC) and organic carbon (OC), play important roles in air quality, human health, and climate change. A better understanding of sources of light-absorbing carbonaceous aerosol (including black carbon and brown carbon) is particular critical for formulating emission-based control strategies and reducing uncertainties in current aerosol radiative forcing estimates. Beijing, the capital of China, has experienced serious air pollution problems and high concentrations of carbonaceous aerosols in recent years, especially during heating seasons. During November and December of 2016, several severe haze episodes occurred in Beijing, with hourly average PM2.5 mass concentration up to 400 μg/m3. In this study, concentration levels and sources of black carbon and brown carbon were investigated based on 7-wavelength Aethalometer (AE-33) with combination of other PM2.5 chemical composition information. Contributions of traffic and non-traffic emissions (e.g., coal combustion, biomass burning) were apportioned, and brown carbon was separated from black carbon. Our preliminary results showed that (1) Concentrations of BC were around 5.3±4.2 μg/m3 during the study period, with distinct diurnal variations during haze and non-haze days. (2) Traffic emissions contributed to about 37±17% of total BC, and exhibited higher contributions during non-haze days compared to haze days. (3) Coal combustion was a major source of black carbon and brown carbon in Beijing, which was more significant compared to biomass burning. Sources and the relative contributions to black carbon and brown carbon during haze and non-haze days will be further discussed.

Dietary carbon sources of mussels and tubeworms from Galapagos hydrothermal vents determined from tissue adC activity

Energy Technology Data Exchange (ETDEWEB)

Williams, P M; Smith, K L; Druffel, E M; Linick, T W

1981-07-30

The large quantities of reduced carbon that are required to support the filter-feeding mytilid mussels (Mytilus sp.), vesicomyid clams (Clayptogena sp.) and various other animals in the Galapagos hydrothermal vent systems are thought to be derived from either the in situ synthesis of particulate organic matter by chemoautotrophic, sulfide-oxidizing bacteria or by the advection of sedimentary organic carbon into the vent environment from surrounding areas. In contrast, the dense populations of vestimentiferan tubeworms (Riftia pachyptila), which lack mouth organs and digestive tracts, apparently utilize organic carbon synthesized by symbiotic chemoautotrophs. We present evidence here, based on adC activities and acC/abC ratios, that the principal source of dietary carbon for mussels and tubeworms is derived from the dissolved inorganic carbon (DIOC) in the vent effluent waters.

Speleothem records of acid sulphate deposition and organic carbon mobilisation

Science.gov (United States)

Wynn, Peter; Fairchild, Ian; Bourdin, Clement; Baldini, James; Muller, Wolfgang; Hartland, Adam; Bartlett, Rebecca

2017-04-01

Dramatic increases in measured surface water DOC in recent decades have been variously attributed to either temperature rise, or destabilisation of long-term soil carbon pools following sulphur peak emissions status. However, whilst both drivers of DOC dynamics are plausible, they remain difficult to test due to the restricted nature of the available records of riverine DOC flux (1978 to present), and the limited availability of SO2 emissions inventory data at the regional scale. Speleothems offer long term records of both sulphur and carbon. New techniques to extract sulphur concentrations and isotopes from speleothem calcite have enabled archives of pollution history and environmental acidification to be reconstructed. Due to the large dynamic range in sulphur isotopic values from end member sources (marine aerosol +21 ‰ to continental biogenic emissions -30 ‰) and limited environmental fractionation under oxidising conditions, sulphur isotopes form an ideal tracer of industrial pollution and environmental acidification in the palaeo-record. We couple this acidification history to the carbon record, using organic matter fluorescence and trace metals. Trace metal ratios and abundance can be used to infer the type and size of organic ligand and are therefore sensitive to changes in temperature as a driver of organic carbon processing and biodegradation. This allows fluorescent properties and ratios of trace metals in speleothem carbonate to be used to represent both the flux of organic carbon into the cave as well as the degradation pathway. Here we present some of the first results of this work, exploring sulphur acidification as a mechanistic control on carbon solubility and export throughout the twentieth century.

Sources and Reactivity of Terrestrial Organic Carbon to the Colville River Delta, Beaufort Sea, Alaska

Science.gov (United States)

Schreiner, K. M.; Bianchi, T. S.; Rosenheim, B. E.

2014-12-01

Terrestrial particulate organic carbon (tPOC) delivery to nearshore deltaic regions is an important mechanism of OC storage and burial, and continental margins worldwide account for approximately 90% of the carbon burial in the ocean. Increasing warming in the Arctic is leading to an acceleration of the hydrologic cycle, warming of permafrost, and broad shifts in vegetation. All of these changes are likely to affect the delivery, reactivity, and burial of tPOC in nearshore Arctic regions, making the Arctic an ideal place to study the effects of climate change on tPOC delivery. However, to date, most studies of tPOC delivery from North America to the Arctic Ocean have focused on large Arctic rivers like the Mackenzie and Yukon, and a significant portion of those watersheds lie in sub-Arctic latitudes, meaning that their tPOC delivery is likely not uniquely representative of the high Arctic tundra. Here, we focus on tPOC delivery by the Colville River, the largest North American river with a watershed that does not include sub-Arctic latitudes. Sediment samples from the river delta and nearby Simpson's Lagoon were taken in August of 2010 and subsequently fractionated by density, in order to study the delivery of both discrete and sediment-sorbed tPOC. Samples were analyzed for stable carbon isotopes, bulk radiocarbon, terrestrial biomarkers (including lignin-phenols, and other CuO reaction products), and aquatic biomarkers (algal pigments), and additionally a subset of the samples were analyzed by ramped pyrolysis-14C. Results show that tPOC delivery near the river mouth is sourced from coastal plain tundra, with additional delivery of tPOC from peat released into the lagoon from the seaward limit of the tundra by coastal erosion. Ramped pyrolysis-14C analysis also shows a clear differentiation between tPOC delivered by the river and tPOC delivered by coastal retreat in the lagoon. Additionally, a significant portion of the OC released by the Colville River is

Optimising carbon and nitrogen sources for Azotobacter ...

African Journals Online (AJOL)

The present work deals with selecting and optimization of carbon and nitrogen sources for producing biomass from Azotobacter chroococcum. Four carbon sources (glucose, sucrose, manitol and sodium benzoate) and four nitrogen sources (yeast extract, meat extract, NH4Cl and (NH4)2SO4) were evaluated during the first ...

Dynamics and sources of reduced sulfur, humic substances and dissolved organic carbon in a temperate river system affected by agricultural practices.

Science.gov (United States)

Marie, Lauriane; Pernet-Coudrier, Benoît; Waeles, Matthieu; Gabon, Marine; Riso, Ricardo

2015-12-15

Although reduced organic sulfur substances (RSS) as well as humic substances (HS) are widely suspected to play a role in, for example, metal speciation or used as a model of dissolved organic carbon (DOC) in laboratory studies, reports of their quantification in natural waters are scarce. We have examined the dynamics and sources of reduced sulfur, HS and DOC over an annual cycle in a river system affected by agricultural practices. The new differential pulse cathodic stripping voltammetry was successfully applied to measure glutathione-like compounds (GSHs), thioacetamide-like compounds (TAs) and the liquid chromatography coupled to organic detector to analyze HS and DOC at high frequency in the Penzé River (NW France). The streamflow-concentration patterns, principal components analysis and flux analysis allowed discrimination of the source of each organic compound type. Surprisingly, the two RSS and HS detected in all samples, displayed different behavior. As previously shown, manuring practice is the main source of DOC and HS in this watershed where agricultural activity is predominant. The HS were then transferred to the river systems via runoff, particularly during the spring and autumn floods, which are responsible of >60% of the annual flux. TAs had a clear groundwater source and may be formed underground, whereas GSHs displayed two sources: one aquagenic in spring and summer probably linked to the primary productivity and a second, which may be related to bacterial degradation. High sampling frequency allowed a more accurate assessment of the flux values which were 280 tC y(-1) for DOC representing 20 kg C ha(-1) y(-1). HS, TAs and GSHs fluxes represented 60, 13, and 4% of the total annual DOC export, respectively. Copyright © 2015 Elsevier B.V. All rights reserved.

Latest Permian carbonate carbon isotope variability traces heterogeneous organic carbon accumulation and authigenic carbonate formation

Science.gov (United States)

Schobben, Martin; van de Velde, Sebastiaan; Gliwa, Jana; Leda, Lucyna; Korn, Dieter; Struck, Ulrich; Vinzenz Ullmann, Clemens; Hairapetian, Vachik; Ghaderi, Abbas; Korte, Christoph; Newton, Robert J.; Poulton, Simon W.; Wignall, Paul B.

2017-11-01

Bulk-carbonate carbon isotope ratios are a widely applied proxy for investigating the ancient biogeochemical carbon cycle. Temporal carbon isotope trends serve as a prime stratigraphic tool, with the inherent assumption that bulk micritic carbonate rock is a faithful geochemical recorder of the isotopic composition of seawater dissolved inorganic carbon. However, bulk-carbonate rock is also prone to incorporate diagenetic signals. The aim of the present study is to disentangle primary trends from diagenetic signals in carbon isotope records which traverse the Permian-Triassic boundary in the marine carbonate-bearing sequences of Iran and South China. By pooling newly produced and published carbon isotope data, we confirm that a global first-order trend towards depleted values exists. However, a large amount of scatter is superimposed on this geochemical record. In addition, we observe a temporal trend in the amplitude of this residual δ13C variability, which is reproducible for the two studied regions. We suggest that (sub-)sea-floor microbial communities and their control on calcite nucleation and ambient porewater dissolved inorganic carbon δ13C pose a viable mechanism to induce bulk-rock δ13C variability. Numerical model calculations highlight that early diagenetic carbonate rock stabilization and linked carbon isotope alteration can be controlled by organic matter supply and subsequent microbial remineralization. A major biotic decline among Late Permian bottom-dwelling organisms facilitated a spatial increase in heterogeneous organic carbon accumulation. Combined with low marine sulfate, this resulted in varying degrees of carbon isotope overprinting. A simulated time series suggests that a 50 % increase in the spatial scatter of organic carbon relative to the average, in addition to an imposed increase in the likelihood of sampling cements formed by microbial calcite nucleation to 1 out of 10 samples, is sufficient to induce the observed signal of carbon

Latest Permian carbonate carbon isotope variability traces heterogeneous organic carbon accumulation and authigenic carbonate formation

Directory of Open Access Journals (Sweden)

M. Schobben

2017-11-01

Full Text Available Bulk-carbonate carbon isotope ratios are a widely applied proxy for investigating the ancient biogeochemical carbon cycle. Temporal carbon isotope trends serve as a prime stratigraphic tool, with the inherent assumption that bulk micritic carbonate rock is a faithful geochemical recorder of the isotopic composition of seawater dissolved inorganic carbon. However, bulk-carbonate rock is also prone to incorporate diagenetic signals. The aim of the present study is to disentangle primary trends from diagenetic signals in carbon isotope records which traverse the Permian–Triassic boundary in the marine carbonate-bearing sequences of Iran and South China. By pooling newly produced and published carbon isotope data, we confirm that a global first-order trend towards depleted values exists. However, a large amount of scatter is superimposed on this geochemical record. In addition, we observe a temporal trend in the amplitude of this residual δ13C variability, which is reproducible for the two studied regions. We suggest that (sub-sea-floor microbial communities and their control on calcite nucleation and ambient porewater dissolved inorganic carbon δ13C pose a viable mechanism to induce bulk-rock δ13C variability. Numerical model calculations highlight that early diagenetic carbonate rock stabilization and linked carbon isotope alteration can be controlled by organic matter supply and subsequent microbial remineralization. A major biotic decline among Late Permian bottom-dwelling organisms facilitated a spatial increase in heterogeneous organic carbon accumulation. Combined with low marine sulfate, this resulted in varying degrees of carbon isotope overprinting. A simulated time series suggests that a 50 % increase in the spatial scatter of organic carbon relative to the average, in addition to an imposed increase in the likelihood of sampling cements formed by microbial calcite nucleation to 1 out of 10 samples, is sufficient to induce the

Elemental and organic carbon in aerosols over urbanized coastal region (southern Baltic Sea, Gdynia).

Science.gov (United States)

Lewandowska, Anita; Falkowska, Lucyna; Murawiec, Dominika; Pryputniewicz, Dorota; Burska, Dorota; Bełdowska, Magdalena

2010-09-15

Studies on PM 10, total particulate matter (TSP), elemental carbon (EC) and organic carbon (OC) concentrations were carried out in the Polish coastal zone of the Baltic Sea, in urbanized Gdynia. The interaction between the land, the air and the sea was clearly observed. The highest concentrations of PM 10, TSP and both carbon fractions were noted in the air masses moving from southern and western Poland and Europe. The EC was generally of primary origin and its contribution to TSP and PM 10 mass was on average 2.3% and 3.7% respectively. Under low wind speed conditions local sources (traffic and industry) influenced increases in elemental carbon and PM 10 concentrations in Gdynia. Elemental carbon demonstrated a pronounced weekly cycle, yielding minimum values at the weekend and maximum values on Thursdays. The role of harbors and ship yards in creating high EC concentrations was clearly observed. Concentration of organic carbon was ten times higher than that of elemental carbon, and the average OC contribution to PM 10 mass was very high (31.6%). An inverse situation was observed when air masses were transported from over the Atlantic Ocean, the North Sea and the Baltic Sea. These clean air masses were characterized by the lowest concentrations of all analysed compounds. Obtained results for organic and elemental carbon fluxes showed that atmospheric aerosols can be treated, along with water run-off, as a carbon source for the coastal waters of the Baltic Sea. The enrichment of surface water was more effective in the case of organic carbon (0.27+/-0.19 mmol m(-2) d(-1)). Elemental carbon fluxes were one order of magnitude smaller, on average 0.03+/-0.04 mmol m(-2) d(-1). We suggest that in some situations atmospheric carbon input can explain up to 18% of total carbon fluxes into the Baltic coastal waters. Copyright 2010 Elsevier B.V. All rights reserved.

Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol

Energy Technology Data Exchange (ETDEWEB)

Massachusetts Institute of Technology; Kroll, Jesse H.; Donahue, Neil M.; Jimenez, Jose L.; Kessler, Sean H.; Canagaratna, Manjula R.; Wilson, Kevin R.; Altieri, Katye E.; Mazzoleni, Lynn R.; Wozniak, Andrew S.; Bluhm, Hendrik; Mysak, Erin R.; Smith, Jared D.; Kolb, Charles E.; Worsnop, Douglas R.

2010-11-05

A detailed understanding of the sources, transformations, and fates of organic species in the environment is crucial because of the central roles that organics play in human health, biogeochemical cycles, and Earth's climate. However, such an understanding is hindered by the immense chemical complexity of environmental mixtures of organics; for example, atmospheric organic aerosol consists of at least thousands of individual compounds, all of which likely evolve chemically over their atmospheric lifetimes. Here we demonstrate the utility of describing organic aerosol (and other complex organic mixtures) in terms of average carbon oxidation state (OSC), a quantity that always increases with oxidation, and is readily measured using state-of-the-art analytical techniques. Field and laboratory measurements of OSC , using several such techniques, constrain the chemical properties of the organics and demonstrate that the formation and evolution of organic aerosol involves simultaneous changes to both carbon oxidation state and carbon number (nC).

The effect of toxic carbon source on the reaction of activated sludge in the batch reactor.

Science.gov (United States)

Wu, Changyong; Zhou, Yuexi; Zhang, Siyu; Xu, Min; Song, Jiamei

2018-03-01

The toxic carbon source can cause higher residual effluent dissolved organic carbon than easily biodegraded carbon source in activated sludge process. In this study, an integrated activated sludge model is developed as the tool to understand the mechanism of toxic carbon source (phenol) on the reaction, regarding the carbon flows during the aeration period in the batch reactor. To estimate the toxic function of phenol, the microbial cells death rate (k death ) is introduced into the model. The integrated model was calibrated and validated by the experimental data and it was found the model simulations matched the all experimental measurements. In the steady state, the toxicity of phenol can result in higher microbial cells death rate (0.1637 h -1 vs 0.0028 h -1 ) and decay rate coefficient of biomass (0.0115 h -1 vs 0.0107 h -1 ) than acetate. In addition, the utilization-associated products (UAP) and extracellular polymeric substances (EPS) formation coefficients of phenol are higher than that of acetate, indicating that more carbon flows into the extracellular components, such as soluble microbial products (SMP), when degrading toxic organics. In the non-steady state of feeding phenol, the yield coefficient for growth and maximum specific growth rate are very low in the first few days (1-10 d), while the decay rate coefficient of biomass and microbial cells death rate are relatively high. The model provides insights into the difference of the dynamic reaction with different carbon sources in the batch reactor. Copyright © 2017 Elsevier Ltd. All rights reserved.

[Organic carbon and carbon mineralization characteristics in nature forestry soil].

Science.gov (United States)

Yang, Tian; Dai, Wei; An, Xiao-Juan; Pang, Huan; Zou, Jian-Mei; Zhang, Rui

2014-03-01

Through field investigation and indoor analysis, the organic carbon content and organic carbon mineralization characteristics of six kinds of natural forest soil were studied, including the pine forests, evergreen broad-leaved forest, deciduous broad-leaved forest, mixed needle leaf and Korean pine and Chinese pine forest. The results showed that the organic carbon content in the forest soil showed trends of gradual decrease with the increase of soil depth; Double exponential equation fitted well with the organic carbon mineralization process in natural forest soil, accurately reflecting the mineralization reaction characteristics of the natural forest soil. Natural forest soil in each layer had the same mineralization reaction trend, but different intensity. Among them, the reaction intensity in the 0-10 cm soil of the Korean pine forest was the highest, and the intensities of mineralization reaction in its lower layers were also significantly higher than those in the same layers of other natural forest soil; comparison of soil mineralization characteristics of the deciduous broad-leaved forest and coniferous and broad-leaved mixed forest found that the differences of litter species had a relatively strong impact on the active organic carbon content in soil, leading to different characteristics of mineralization reaction.

Elucidating the Role of Carbon Sources on Abiotic and Biotic Release of Arsenic into Cambodian Aquifers

Science.gov (United States)

Koeneke, M.

2017-12-01

Arsenic (As) is a naturally occurring contaminant in Cambodia that has been contaminating well-water sources of millions of people. Commonly, studies look into the biotic factors that cause the arsenic to be released from aquifer sediments to groundwater. However, abiotic release of As from sediments, though little studied, may also play key roles in As contamination of well water. The goal of this research is to quantitatively compare organic-carbon mediated abiotic and biotic release of arsenic from sediments to groundwater. Batch anaerobic incubation experiments under abiotic (sodium azide used to immobilize microbes) and biotic conditions were conducted using Cambodian aquifer sediments, four different organic carbon sources (sodium lactate, sodium citrate, sodium oxalate, and humic acid), and six different carbon concentrations (0, 1, 2.5, 5, 10, 25mg C/L). Dissolved arsenic, iron(Fe), and manganese(Mn) concentrations in the treatments were measured 112 days . In addition, sediment and solution carbon solution was measured . Collectively, these show how different carbon sources, different carbon concentrations, and how abiotic and biotic factors impact the release of arsenic from Cambodian sediments into aquifers. Overall, an introduction of organic carbon to the soil increases the amount of As released from the sediment. The biotic + abiotic and abiotic conditions seemed to play a minimal role in the amount of As released. Dissolved species analysis showed us that 100% of the As was As(V), Our ICP-MS results vary due to the heterogeneity of samples, but when high levels are Fe are seen in solution, we also see high levels of As. We also see higher As concentrations when there is a smaller amount of Mn in solution.

Organic electrochemistry and carbon electrodes

International Nuclear Information System (INIS)

Weinberg, N.

1983-01-01

Carbons are often used in organic electrosynthesis and are critical as anodes or cathodes to certain reactions. Too often the surface properties of carbons have been left uncharacterized in relation to the reaction; however, these physical and chemical properties of carbons are important to the nature of the products, and the selectivity. Examples presented include the Kolbe reaction, the oxidation of aromatics in presence of carboxylate salts, electrofluorination of organics, acetamidation of aromatics, the hydrodimerization of formaldehyde and the oxidation of carbon fibers. These reactions apparently involve special surface characteristics: structure, surface area, stabilized surface sites, and the presence or absence of significant ''oxide'' functionality

Organic carbon organic matter and bulk density relationships in arid ...

African Journals Online (AJOL)

Soil organic matter (SOM) and soil organic carbon (SOC) constitute usually a small portion of soil, but they are one of the most important components of ecosystems. Bulk density (dB or BD) value is necessary to convert organic carbon (OC) content per unit area. Relationships between SOM, SOC and BD were established ...

Organics in environmental ices: sources, chemistry, and impacts

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V. F. McNeill

2012-10-01

Full Text Available The physical, chemical, and biological processes involving organics in ice in the environment impact a number of atmospheric and biogeochemical cycles. Organic material in snow or ice may be biological in origin, deposited from aerosols or atmospheric gases, or formed chemically in situ. In this manuscript, we review the current state of knowledge regarding the sources, properties, and chemistry of organic materials in environmental ices. Several outstanding questions remain to be resolved and fundamental data gathered before an accurate model of transformations and transport of organic species in the cryosphere will be possible. For example, more information is needed regarding the quantitative impacts of chemical and biological processes, ice morphology, and snow formation on the fate of organic material in cold regions. Interdisciplinary work at the interfaces of chemistry, physics and biology is needed in order to fully characterize the nature and evolution of organics in the cryosphere and predict the effects of climate change on the Earth's carbon cycle.

Acidity controls on dissolved organic carbon mobility in organic soils

Czech Academy of Sciences Publication Activity Database

Evans, Ch. D.; Jones, T.; Burden, A.; Ostle, N.; Zielinski, P.; Cooper, M.; Peacock, M.; Clark, J.; Oulehle, Filip; Cooper, D.; Freeman, Ch.

2012-01-01

Roč. 18, č. 11 (2012), s. 3317-3331 ISSN 1354-1013 Institutional support: RVO:67179843 Keywords : acidity * dissolved organic carbon * organic soil * peat * podzol * soil carbon * sulphur Subject RIV: EH - Ecology, Behaviour Impact factor: 6.910, year: 2012

River Export of Dissolved and Particulate Organic Carbon from Permafrost and Peat Deposits across the Siberian Arctic

Science.gov (United States)

Wild, B.; Andersson, A.; Bröder, L.; Vonk, J.; Hugelius, G.; McClelland, J. W.; Raymond, P. A.; Gustafsson, O.

2017-12-01

Permafrost and peat deposits of northern high latitudes store more than 1300 Pg of organic carbon. This carbon has been preserved for thousands of years by cold and moist conditions, but is now increasingly mobilized as temperatures rise. While part will be degraded to CO2 and CH4 and amplify global warming, part will be exported by rivers to the Arctic Ocean where it can be degraded or re-buried by sedimentation. We here use the four large Siberian rivers Ob, Yenisey, Lena, and Kolyma as natural integrators of carbon mobilization in their catchments. We apply isotope based source apportionments and Markov Chain Monte Carlo Simulations to quantify contributions of organic carbon from permafrost and peat deposits to organic carbon exported by these rivers. More specifically, we compare the 14C signatures of dissolved and particulate organic carbon (DOC, POC) sampled close to the river mouths with those of five potential carbon sources; (1) recent aquatic and (2) terrestrial primary production, (3) the active layer of permafrost soils, (4) deep Holocene deposits (including thermokarst and peat deposits) and (5) Ice Complex Deposits. 14C signatures of these endmembers were constrained based on extensive literature review. We estimate that the four rivers together exported 2.4-4.5 Tg organic carbon from permafrost and peat deposits per year. While total organic carbon export was dominated by DOC (90%), the export of organic carbon from permafrost and peat deposits was more equally distributed between DOC (56%) and POC (44%). Recent models predict that ca. 200 Pg carbon will be lost as CO2 or CH4 by 2100 (RCP8.5) from the circumarctic permafrost area, of which roughly a quarter is drained by the Ob, Yenisey, Lena, and Kolyma rivers. Our comparatively low estimates of river carbon export thus suggest limited transfer of organic carbon from permafrost and peat deposits to high latitude rivers, or its rapid degradation within rivers. Our findings highlight the importance

Source apportionment of fine organic aerosol in Mexico City during the MILAGRO experiment 2006

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E. A. Stone

2008-03-01

Full Text Available Organic carbon (OC comprises a large fraction of fine particulate matter (PM_2.5 in Mexico City. Daily and select 12-h PM_2.5 samples were collected in urban and peripheral sites in Mexico City from 17–30 March 2006. Samples were analyzed for OC and elemental carbon (EC using thermal-optical filter-based methods. Real-time water-soluble organic carbon (WSOC was collected at the peripheral site. Organic compounds, particularly molecular markers, were quantified by soxhlet extraction with methanol and dichloromethane, derivitization, and gas chromatography with mass spectrometric detection (GCMS. A chemical mass balance model (CMB based on molecular marker species was used to determine the relative contribution of major sources to ambient OC. Motor vehicles, including diesel and gasoline, consistently accounted for 49% of OC in the urban area and 32% on the periphery. The daily contribution of biomass burning to OC was highly variable, and ranged from 5–26% at the urban site and 7–39% at the peripheral site. The remaining OC unapportioned to primary sources showed a strong correlation with WSOC and was considered to be secondary in nature. Comparison of temporally resolved OC showed that contributions from primary aerosol sources during daylight hours were not significantly different from nighttime. This study provides quantitative understanding of the important sources of OC during the MILAGRO 2006 field campaign.

Organic carbon spiralling in stream ecosystems

Energy Technology Data Exchange (ETDEWEB)

Newbold, J D; Mulholland, P J; Elwood, J W; O' Neill, R V

1982-01-01

The term spiralling has been used to describe the combined processes of cycling and longitudinal transport in streams. As a measure or organic carbon spiralling, we introduced organic carbon turnover length, S, defined as the average or expected downstream distance travelled by a carbon atom between its entry or fixation in the stream and its oxidation. Using a simple model for organic carbon dynamics in a stream, we show that S is closely related to fisher and Likens' ecosystem efficiency. Unlike efficiency, however, S is independent of the length of the study reach, and values of S determined in streams of differing lengths can be compared. Using data from three different streams, we found the relationship between S and efficiency to agree closely with the model prediction. Hypotheses of stream functioning are discussed in the context of organic carbeon spiralling theory.

Diagnostic Evaluation of Carbon Sources in CMAQ

Science.gov (United States)

Traditional monitoring networks measure only total elemental carbon (EC) and organic carbon (OC) routinely. Diagnosing model biases with such limited information is difficult. Measurements of organic tracer compounds have recently become available and allow for more detailed di...

Effect of additional carbon source on naphthalene biodegradation by Pseudomonas putida G7

International Nuclear Information System (INIS)

Lee, Kangtaek; Park, Jin-Won; Ahn, Ik-Sung

2003-01-01

Addition of a carbon source as a nutrient into soil is believed to enhance in situ bioremediation by stimulating the growth of microorganisms that are indigenous to the subsurface and are capable of degrading contaminants. However, it may inhibit the biodegradation of organic contaminants and result in diauxic growth. The objective of this work is to study the effect of pyruvate as another carbon source on the biodegradation of polynuclear aromatic hydrocarbons (PAHs). In this study, naphthalene was used as a model PAH, ammonium sulfate as a nitrogen source, and oxygen as an electron acceptor. Pseudomonas putida G7 was used as a model naphthalene-degrading microorganism. From a chemostat culture, the growth kinetics of P. putida G7 on pyruvate was determined. At concentrations of naphthalene and pyruvate giving similar growth rates of P. putida G7, diauxic growth of P. putida G7 was not observed. It is suggested that pyruvate does not inhibit naphthalene biodegradation and can be used as an additional carbon source to stimulate the growth of P. putida G7 that can degrade polynuclear aromatic hydrocarbons

Mobility of organic carbon from incineration residues

International Nuclear Information System (INIS)

Ecke, Holger; Svensson, Malin

2008-01-01

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 6-1 experimental design. Controlled factors were treatment with ultrasonic radiation, full carbonation (addition of CO 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

State-Space Estimation of Soil Organic Carbon Stock

Science.gov (United States)

Ogunwole, Joshua O.; Timm, Luis C.; Obidike-Ugwu, Evelyn O.; Gabriels, Donald M.

2014-04-01

Understanding soil spatial variability and identifying soil parameters most determinant to soil organic carbon stock is pivotal to precision in ecological modelling, prediction, estimation and management of soil within a landscape. This study investigates and describes field soil variability and its structural pattern for agricultural management decisions. The main aim was to relate variation in soil organic carbon stock to soil properties and to estimate soil organic carbon stock from the soil properties. A transect sampling of 100 points at 3 m intervals was carried out. Soils were sampled and analyzed for soil organic carbon and other selected soil properties along with determination of dry aggregate and water-stable aggregate fractions. Principal component analysis, geostatistics, and state-space analysis were conducted on the analyzed soil properties. The first three principal components explained 53.2% of the total variation; Principal Component 1 was dominated by soil exchange complex and dry sieved macroaggregates clusters. Exponential semivariogram model described the structure of soil organic carbon stock with a strong dependence indicating that soil organic carbon values were correlated up to 10.8m.Neighbouring values of soil organic carbon stock, all waterstable aggregate fractions, and dithionite and pyrophosphate iron gave reliable estimate of soil organic carbon stock by state-space.

Sources and compositional distribution of organic carbon in surface sediments from the lower Pearl River to the coastal South China Sea

Science.gov (United States)

Li, X.; Zhang, Z.; Wade, T.; Knap, A. H.; Zhang, C.

2017-12-01

The Pearl River plays an important role in transporting terrestrial organic carbon (OC) to the South China Sea (SCS). However, the sources and compositional distribution of OC in the system are poorly understood. This study focused on delineating the sources and determining the fate of surface sedimentary OC from the Feilaixia Hydro-power Station to the coastal SCS. Elemental, stable carbon/nitrogen isotope (δ13C, δ15N) and lignin-phenol analyses have been conducted. The total OC (TOC) from the up-stream sites were generally derived from vascular plants (higher C/N, and depleted δ13C) and soils. Additional input was attributed to riverine primary production (lower C/N and enriched δ13C), which was enhanced near the dam-created reservoir. The C/N and δ13C values were not significantly different among sites in the mid-stream. The estuary/coastal sites witnessed hydrodynamically sorted riverine OC, which was diluted by marine primary production (lower C/N and more enriched δ13C). The lignin concentration was the highest in the up-stream sites, remained relatively unchanged in the mid-stream sites and decreased significantly along the estuary/coastal sites, which was corroborated by variation in TOC. A comprehensive five-endmember Monte Carlo simulation suggested that previous studies had underestimated the C4 plant input by 14 ± 11% and overestimated the riverbank soil input by 21 ± 17%. Thus, our study provided valuable information for more accurate source and mass balance studies of terrestrial OC transported to the SCS, which helped to further understand the carbon cycling in the large river-ocean continuum.

Differential responses of sugar, organic acids and anthocyanins to source-sink modulation in Cabernet Sauvignon and Sangiovese grapevines.

Science.gov (United States)

Bobeica, Natalia; Poni, Stefano; Hilbert, Ghislaine; Renaud, Christel; Gomès, Eric; Delrot, Serge; Dai, Zhanwu

2015-01-01

Grape berry composition mainly consists of primary and secondary metabolites. Both are sensitive to environment and viticultural management. As a consequence, climate change can affect berry composition and modify wine quality and typicity. Leaf removal techniques can impact berry composition by modulating the source-to-sink balance and, in turn, may mitigate some undesired effects due to climate change. The present study investigated the balance between technological maturity parameters such as sugars and organic acids, and phenolic maturity parameters such as anthocyanins in response to source-sink modulation. Sugar, organic acid, and anthocyanin profiles were compared under two contrasting carbon supply levels in berries of cv. Cabernet Sauvignon and Sangiovese collected at 9 and 14 developmental stages respectively. In addition, whole-canopy net carbon exchange rate was monitored for Sangiovese vines and a mathematic model was used to calculate the balance between carbon fixation and berry sugar accumulation. Carbon limitation affected neither berry size nor the concentration of organic acids at harvest. However, it significantly reduced the accumulation of sugars and total anthocyanins in both cultivars. Most interestingly, carbon limitation decreased total anthocyanin concentration by 84.3% as compared to the non source-limited control, whereas it decreased sugar concentration only by 27.1%. This suggests that carbon limitation led to a strong imbalance between sugars and anthocyanins. Moreover, carbon limitation affected anthocyanin profiles in a cultivar dependent manner. Mathematical analysis of carbon-balance indicated that berries used a higher proportion of fixed carbon for sugar accumulation under carbon limitation (76.9%) than under carbon sufficiency (48%). Thus, under carbon limitation, the grape berry can manage the metabolic fate of carbon in such a way that sugar accumulation is maintained at the expense of secondary metabolites.

Differential responses of sugar, organic acids and anthocyanins to source-sink modulation in Cabernet Sauvignon and Sangiovese grapevines

Directory of Open Access Journals (Sweden)

Natalia eBobeica

2015-05-01

Full Text Available Grape berry composition mainly consists of primary and secondary metabolites. Both are sensitive to environment and viticultural management. As a consequence, climate change can affect berry composition and modify wine quality and typicity. Leaf removal techniques can impact berry composition by modulating the source-to-sink balance and, in turn, may mitigate some undesired effects due to climate change. The present study investigated the balance between technological maturity parameters such as sugars and organic acids, and phenolic maturity parameters such as anthocyanins in response to source-sink modulation. Sugar, organic acid, and anthocyanin profiles were compared under two contrasting carbon supply levels in berries of cv. Cabernet Sauvignon and Sangiovese collected at 9 and 14 developmental stages respectively. In addition, whole-canopy net carbon exchange rate was monitored for Sangiovese vines and a mathematic model was used to calculate the balance between carbon fixation and berry sugar accumulation. Carbon limitation affected neither berry size nor the concentration of organic acids at harvest. However, it significantly reduced the accumulation of sugars and total anthocyanins in both cultivars. Most interestingly, carbon limitation decreased total anthocyanin concentration by 84.3 % as compared to the non source-limited control, whereas it decreased sugar concentration only by 27.1 %. This suggests that carbon limitation led to a strong imbalance between sugars and anthocyanins. Moreover, carbon limitation affected anthocyanin profiles in a cultivar dependent manner. Mathematical analysis of carbon-balance indicated that berries used a higher proportion of fixed carbon for sugar accumulation under carbon limitation (76.9% than under carbon sufficiency (48%. Thus, under carbon limitation, the grape berry can manage the metabolic fate of carbon in such a way that sugar accumulation is maintained at the expense of secondary

Growth and sporulation of Trichoderma polysporum on organic substrates by addition of carbon and nitrogen sources

International Nuclear Information System (INIS)

Rajput, A.Q.; Shahzad, S.

2015-01-01

During the present study nine different organic substrates viz., rice grains, sorghum grains, wheat grains, millet grains, wheat straw, rice husk, cow dung, sawdust and poultry manure were used for mass multiplication of Trichoderma polysporum. Grains, especially sorghum grains were found to be the best substrate for T. polysporum. Wheat straw and rice husk were less suitable, whereas, cow dung, sawdust and poultry manure were not suitable for growth of the fungus. Sucrose at the rate of 30,000 ppm and ammonium nitrate at the rate of 3,000 ppm were found to be the best carbon and nitrogen sources for growth and sporulation of T. polysporum. Amendment of the selected C and N sources to wheat straw, rice husk and millet grains resulted in significantly higher growth and conidia production by T. polysporum as compared to un-amended substrates. Sorghum and rice grains showed suppression in growth and sporulation of T. polysporum when amended with C and N sources. During studies on shelf life, populations of T. polysporum attained the peck at 60-135 days intervals on different substrates and declined gradually thereafter. However, even after 330 days, the populations were greater than the population at 0-day. At 345-360 days interval, populations were less than the initial populations at 0- days. Shelf life on C+N amended wheat straw and rice husk were more as compared to un-amended substrates. (author)

Russia's black carbon emissions: focus on diesel sources

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N. Kholod

2016-09-01

Full Text Available Black carbon (BC is a significant climate forcer with a particularly pronounced forcing effect in polar regions such as the Russian Arctic. Diesel combustion is a major global source of BC emissions, accounting for 25–30 % of all BC emissions. While the demand for diesel is growing in Russia, the country's diesel emissions are poorly understood. This paper presents a detailed inventory of Russian BC emissions from diesel sources. Drawing on a complete Russian vehicle registry with detailed information about vehicle types and emission standards, this paper analyzes BC emissions from diesel on-road vehicles. We use the COPERT emission model (COmputer Programme to calculate Emissions from Road Transport with Russia-specific emission factors for all types of on-road vehicles. On-road diesel vehicles emitted 21 Gg of BC in 2014: heavy-duty trucks account for 60 % of the on-road BC emissions, while cars represent only 5 % (light commercial vehicles and buses account for the remainder. Using Russian activity data and fuel-based emission factors, the paper also presents BC emissions from diesel locomotives and ships, off-road engines in industry, construction and agriculture, and generators. The study also factors in the role of superemitters in BC emissions from diesel on-road vehicles and off-road sources. The total emissions from diesel sources in Russia are estimated to be 49 Gg of BC and 17 Gg of organic carbon (OC in 2014. Off-road diesel sources emitted 58 % of all diesel BC in Russia.

Carbon Composition of Particulate Organic Carbon in the Gulf of Mexico

Science.gov (United States)

Rogers, K.; Montoya, J. P.; Weber, S.; Bosman, S.; Chanton, J.

2016-02-01

The Deepwater Horizon blowout released 5.0x1011 g C from gaseous hydrocarbons and up to 6.0x1011g C from oil into the water column. Another carbon source, adding daily to the water column, leaks from the natural hydrocarbon seeps that pepper the seafloor of the Gulf of Mexico. How much of this carbon from the DWH and natural seeps is assimilated into particulate organic carbon (POC) in the water column? We filtered seawater collected in 2010, 2012, and 2013 from seep and non-seep sites, collecting POC on 0.7µm glass microfiber filters and analyzing the POC for stable and radiocarbon isotopes. Mixing models based on carbon isotopic endmembers of methane, oil, and modern production were used to estimate the percentage of hydrocarbon incorporated into POC. Significant differences were seen between POC from shallow and deep waters and between POC collected from seep, non-seep, and blowout sites; however yearly differences were not as evident suggesting the GOM has a consistent supply of depleted carbon. Stable carbon isotopes signatures of POC in the Gulf averaged -23.7±2.5‰ for shallow samples and -26.65±2.9‰ for deep POC samples, while radiocarbon signatures averaged -100.4±146.1‰ for shallow and -394.6±197‰ for deep samples. POC in the northern Gulf are composed of 23-91% modern carbon, 2-21% methane, and 0-71% oil. Oil plays a major role in the POC composition of the GOM, especially at the natural seep GC600.

Spontaneous arylation of activated carbon from aminobenzene organic acids as source of diazonium ions in mild conditions

International Nuclear Information System (INIS)

Lebègue, Estelle; Brousse, Thierry; Gaubicher, Joël; Cougnon, Charles

2013-01-01

Activated carbon products modified with benzoic, benzenesulfonic and benzylphosphonic acid groups were prepared by spontaneous reduction of aryldiazonium ions in situ generated in water from the corresponding aminobenzene organic acids without addition of an external acid. Electrochemistry and NMR studies show that the advancement of the diazotization reaction depends both on the acidity and the electronic effect of the organic acid substituent, giving a mixture of diazonium, amine and triazene functionalities. Carbon products prepared by reaction of activated carbon Norit with 4-aminobenzenecarboxylic acid, 4-aminobenzenesulfonic acid and (4-aminobenzyl)phosphonic acid were analyzed by chemical elemental analysis and X-ray photoelectron spectroscopy experiments. Results show that this strategy is well suited for the chemical functionalization, giving a maximized grafting yield due to a chemical cooperation of amine and diazonium functionalities

Spatial distribution of soil organic carbon stocks in France

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M. P. Martin

2011-05-01

Full Text Available 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

Burial fluxes and source apportionment of carbon in culture areas of Sanggou Bay over the past 200 years

Institute of Scientific and Technical Information of China (English)

LIU Sai; HUANG Jiansheng; YANG Qian; YANG Shu; YANG Guipeng; SUN Yao

2015-01-01

In this study, we assessed the burial fluxes and source appointment of different forms of carbon in core sediments collected from culture areas in the Sanggou Bay, and preliminarily analyzed the reasons for the greater proportion of inorganic carbon burial fluxes (BFTIC). The average content of total carbon (TC) in the Sanggou Bay was 2.14%. Total organic carbon (TOC) accounted for a small proportion in TC, more than 65% of which derived from terrigenous organic carbon (Ct), and while the proportion of marine-derived organic carbon (Ca) increased significantly since the beginning of large-scale aquaculture. Total inorganic carbon (TIC) accounted for 60%–75%of TC, an average of which was 60%, with a maximum up to 90% during flourishing periods (1880–1948) of small natural shellfish derived from seashells inorganic carbon (Shell-IC). The TC burial fluxes ranged from 31 g/(m2·a) to 895 g/(m2·a) with an average of 227 g/(m2·a), which was dominated by TIC (about 70%). Shell-IC was the main source of TIC and even TC. As the main food of natural shellfish, biogenic silica (BSi) negatively correlated with BFTIC through affecting shellfish breeding. BFTIC of Sta. S1, influenced greatly by the Yellow Sea Coastal Current, had a certain response to Pacific Decadal Oscillation (PDO) in some specific periods.

Temperature dependence of photodegradation of dissolved organic matter to dissolved inorganic carbon and particulate organic carbon

Czech Academy of Sciences Publication Activity Database

Porcal, Petr; Dillon, P. J.; Molot, L. A.

2015-01-01

Roč. 10, č. 6 (2015), e0128884 E-ISSN 1932-6203 R&D Projects: GA ČR(CZ) GAP503/12/0781; GA ČR(CZ) GA15-09721S Institutional support: RVO:60077344 Keywords : dissolved organic carbon * particulate organic carbon * photodegradation * temperature Subject RIV: DA - Hydrology ; Limnology Impact factor: 3.057, year: 2015

Pyroclastic Eruption Boosts Organic Carbon Fluxes Into Patagonian Fjords

Science.gov (United States)

Mohr, Christian H.; Korup, Oliver; Ulloa, Héctor; Iroumé, Andrés.

2017-11-01

Fjords and old-growth forests store large amounts of organic carbon. Yet the role of episodic disturbances, particularly volcanic eruptions, in mobilizing organic carbon in fjord landscapes covered by temperate rainforests remains poorly quantified. To this end, we estimated how much wood and soils were flushed to nearby fjords following the 2008 eruption of Chaitén volcano in south-central Chile, where pyroclastic sediments covered >12 km2 of pristine temperate rainforest. Field-based surveys of forest biomass, soil organic content, and dead wood transport reveal that the reworking of pyroclastic sediments delivered 66,500 + 14,600/-14,500 tC of large wood to two rivers entering the nearby Patagonian fjords in less than a decade. A similar volume of wood remains in dead tree stands and buried beneath pyroclastic deposits ( 79,900 + 21,100/-16,900 tC) or stored in active river channels (5,900-10,600 tC). We estimate that bank erosion mobilized 132,300+21,700/-30,600 tC of floodplain forest soil. Eroded and reworked forest soils have been accreting on coastal river deltas at >5 mm yr-1 since the eruption. While much of the large wood is transported out of the fjord by long-shore drift, the finer fraction from eroded forest soils is likely to be buried in the fjords. We conclude that the organic carbon fluxes boosted by rivers adjusting to high pyroclastic sediment loads may remain elevated for up to a decade and that Patagonian temperate rainforests disturbed by excessive loads of pyroclastic debris can be episodic short-lived carbon sources.

Is black carbon a better predictor of polycyclic aromatic hydrocarbon distribution in soils than total organic carbon?

International Nuclear Information System (INIS)

Agarwal, Tripti; Bucheli, Thomas D.

2011-01-01

Black carbon (BC) and total organic carbon (TOC) were quantified in the surface soils of Switzerland (N = 105) and Delhi (N = 36), India, to examine their relationships with contents of polycyclic aromatic hydrocarbons (PAH). BC content in Swiss (background) soils (N = 104) varied from 0.41 to 4.75 mg/g (median: 1.13 mg/g) and constituted 1-9% (median: 3%) of TOC. Indian (urban) soils had similar BC concentrations (0.37-2.05 mg/g, median: 1.19 mg/g), with relatively higher BC/TOC (6-23%, median: 13%). Similar to TOC, BC showed significant positive correlation with lighter PAH, but no correlation with heavier PAH in Swiss soils. In contrast, heavier PAH were significantly correlated only with BC in Delhi soils. It seems that TOC governs the distribution of PAH in organic matter rich background soils, while the proximity to emission sources is reflected by BC-PAH association in urban soils. - Light PAH correlated with TOC in background soils, whereas heavy PAH were associated with BC close to emission sources.

Source apportionment of fine organic aerosols in Beijing

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S. Guo

2009-11-01

Full Text Available Fine particles (PM_2.5, i.e., particles with an aerodynamic diameter of ≤2.5 μm were collected from the air in August 2005, August–September 2006, and January–February 2007, in Beijing, China. The chemical compositions of particulate organic matter in the ambient samples were quantified by gas chromatography/mass spectrometry. The dominant compounds identified in summertime were n-alkanoic acids, followed by dicarboxylic acids and sugars, while sugars became the most abundant species in winter, followed by polycyclic aromatic hydrocarbons, n-alkanes, and n-alkanoic acids. The contributions of seven emission sources (i.e., gasoline/diesel vehicles, coal burning, wood/straw burning, cooking, and vegetative detritus to particulate organic matter in PM_2.5 were estimated using a chemical mass balance receptor model. The model results present the seasonal trends of source contributions to organic aerosols. Biomass burning (straw and wood had the highest contribution in winter, followed by coal burning, vehicle exhaust, and cooking. The contribution of cooking was the highest in summer, followed by vehicle exhaust and biomass burning, while coal smoke showed only a minor contribution to ambient organic carbon.

Effect of various carbon and nitrogen sources on cellulose synthesis ...

African Journals Online (AJOL)

The effect of various carbon and nitrogen sources on cellulose production by Acetobacter lovaniensis HBB5 was examined. In this study, glucose, fructose, sucrose and ethanol as carbon source and yeast extract, casein hydrolysate and ammonium sulphate as nitrogen source were used. Among the carbon sources, ...

Effects of nitrogen and carbon sources on the production of inulinase from strain Bacillus sp. SG113

Science.gov (United States)

Gavrailov, Simeon; Ivanova, Viara

2016-03-01

The effects of the carbon and nitrogen substrates on the growth of Bacillus sp. SG113 strain were studied. The use of organic nitrogen sources (peptone, beef extract, yeast extract, casein) leads to rapid cellular growth and the best results for the Bacillus strain were obtained with casein hydrolysate. From the inorganic nitrogen sources studied, the (NH4) 2SO4 proved to be the best nitrogen source. Casein hydrolysate and (NH4) 2SO4 stimulated the invertase synthesis. In the presence of Jerusalem artichoke, onion and garlic extracts as carbon sources the strain synthesized from 6 to 10 times more inulinase.

Geophysical Prediction Technology Based on Organic Carbon Content in Source Rocks of the Huizhou Sag, the South China Sea

Directory of Open Access Journals (Sweden)

Yang Wei

2017-08-01

Full Text Available Due to the high exploration cost, limited number of wells for source rocks drilling and scarce test samples for the Total Organic Carbon Content (TOC in the Huizhou sag, the TOC prediction of source rocks in this area and the assessment of resource potentials of the basin are faced with great challenges. In the study of TOC prediction, predecessors usually adopted the logging assessment method, since the data is only confined to a “point” and the regional prediction of the source bed in the seismic profile largely depends on the recognition of seismic facies, making it difficult to quantify TOC. In this study, we combined source rock geological characteristics, logging and seismic response and built the mathematical relation between quasi TOC curve and seismic data based on the TOC logging date of a single well and its internal seismic attribute. The result suggested that it was not purely a linear relationship that was adhered to by predecessors, but was shown as a complicated non-linear relationship. Therefore, the neural network algorithm and SVMs were introduced to obtain the optimum relationship between the quasi TOC curve and the seismic attribute. Then the goal of TOC prediction can be realized with the method of seismic inversion.

Modelling the role of algae in rice crop nutrition and soil organic carbon maintenance

NARCIS (Netherlands)

Gaydon, D.S.; Probert, M.E.; Buresh, R.J.; Meinke, H.B.; Timsina, J.

2012-01-01

Photosynthetic aquatic biomass (PAB – algae and other floodwater flora) is a significant source of organic carbon (C) in rice-based cropping systems. A portion of PAB is capable of fixing nitrogen (N), and is hence also a source of N for crop nutrition. To account for this phenomenon in long term

[Distribution and source of particulate organic carbon and particulate nitrogen in the Yangtze River Estuary in summer 2012].

Science.gov (United States)

Xing, Jian-Wei; Xian, Wei-Wei; Sheng, Xiu-Zhen

2014-07-01

Based on the data from the cruise carried out in August 2012 in the Yangtze River Estuary and its adjacent waters, spatial distributions of particulate organic carbon (POC), particulate nitrogen (PN) and their relationships with environmental factors were studied, and the source of POC and the contribution of phytoplankton to POC were analyzed combined with n (C)/n (N) ratio and chlorophyll a (Chl a) in the Yangtze River Estuary in summer 2012. The results showed that the concentrations of POC in the Yangtze River Estuary ranged from 0.68 mg x L(-1) to 34.80 mg x L(-1) in summer and the average content was 3.74 mg x L(-1), and PN contents varied between 0.03 mg x L(-1) and 9.13 mg x L(-1) with an average value of 0.57 mg x L(-1). Both of them presented that the concentrations in bottom layers were higher than those in the surface. POC and PN as well as total suspended matter (TSM) showed a extremel similar horizontal distribution trend that the highest values appeared in the near of the mouth and southwest of the survey waters, and decreased rapidly as toward the open seas, both of them showed higher contents in coastal zones and lower in outer sea. There was a fairly good positive linear relationship between POC and PN, which indicated that they had the same source. POC and PN expressed significantly positive correlations with TSM and chemical oxygen demand (COD), but showed relatively weak correlations with salinit and chlorophyll a, which demonstrated that terrestrial inputs had a strong influence on the distribution of POC and PN, and phytoplankton production was not the major source of organic matters in the Yangtze River Estuary. Both the n (C)/n (N) ratio and POC/Chl a analysis showed that the main source of POC was terrestrial inputs, and organic debris was the main existence form of POC. Quantitative analysis showed the biomass of phytoplankton only made an average of 2.54% contribution to POC in the Yangtze Rive Estuary in summer and non-living POC

Large contribution of fossil fuel derived secondary organic carbon to water soluble organic aerosols in winter haze in China

Science.gov (United States)

Zhang, Yan-Lin; El-Haddad, Imad; Huang, Ru-Jin; Ho, Kin-Fai; Cao, Jun-Ji; Han, Yongming; Zotter, Peter; Bozzetti, Carlo; Daellenbach, Kaspar R.; Slowik, Jay G.; Salazar, Gary; Prévôt, André S. H.; Szidat, Sönke

2018-03-01

Water-soluble organic carbon (WSOC) is a large fraction of organic aerosols (OA) globally and has significant impacts on climate and human health. The sources of WSOC remain very uncertain in polluted regions. Here we present a quantitative source apportionment of WSOC, isolated from aerosols in China using radiocarbon (14C) and offline high-resolution time-of-flight aerosol mass spectrometer measurements. Fossil emissions on average accounted for 32-47 % of WSOC. Secondary organic carbon (SOC) dominated both the non-fossil and fossil derived WSOC, highlighting the importance of secondary formation to WSOC in severe winter haze episodes. Contributions from fossil emissions to SOC were 61 ± 4 and 50 ± 9 % in Shanghai and Beijing, respectively, significantly larger than those in Guangzhou (36 ± 9 %) and Xi'an (26 ± 9 %). The most important primary sources were biomass burning emissions, contributing 17-26 % of WSOC. The remaining primary sources such as coal combustion, cooking and traffic were generally very small but not negligible contributors, as coal combustion contribution could exceed 10 %. Taken together with earlier 14C source apportionment studies in urban, rural, semi-urban and background regions in Asia, Europe and the USA, we demonstrated a dominant contribution of non-fossil emissions (i.e., 75 ± 11 %) to WSOC aerosols in the Northern Hemisphere; however, the fossil fraction is substantially larger in aerosols from East Asia and the eastern Asian pollution outflow, especially during winter, due to increasing coal combustion. Inclusion of our findings can improve a modelling of effects of WSOC aerosols on climate, atmospheric chemistry and public health.

CO₂ and O₂ respiration kinetics in hydrocarbon contaminated soils amended with organic carbon sources used to determine catabolic diversity.

Science.gov (United States)

Pietravalle, Stéphane; Aspray, Thomas J

2013-05-01

Multiple substrate induced respiration (MSIR) assays which assess the response of soils to carbon source amendment are effective approaches to determine catabolic diversity of soils. Many assays are based on a single short term (hydrocarbon contaminated soils using continuous CO2 and O2 respiration measurements. Based on cumulative CO2 and O2 measurements at 4, 24 and 120 h, the soils were found to be distinct in terms of their catabolic diversity. Most noteworthy, however, was the response to the addition of maleic acid which provided strong evidence of abiotic CO2 efflux to be the overriding process, raising questions about the interpretation of CO2 only responses from organic acid addition in MSIR assays. Copyright © 2013 Elsevier Ltd. All rights reserved.

Carbon source recovery from excess sludge by mechanical disintegration for biological denitrification.

Science.gov (United States)

Zubrowska-Sudol, M

2018-04-01

The goal of the study was to evaluate the possibility of carbon source recovery from excess sludge by mechanical disintegration for biological denitrification. The total efficiency of denitrification, unit demand for organic compounds for denitrification, unit volume of disintegrated sludge and unit cost of nitrogen removal as a function of energy density used for excess sludge disintegration (70, 140 and 210 kJ/L) were analyzed. In the study a full-scale disc disintegrator was used (motor power: 30 kWh, motor speed: 2,950 rpm). It was shown that the amounts of organic compounds released from the activated sludge flocs at all tested levels of energy density are high enough to be used to intensify the removal of nitrogen compounds from wastewater. It was also documented that the energy density provided during process of disintegration was an important factor determining the characteristics of organic compounds obtained under the disintegration for their use in order to intensify the process of denitrification. The highest value of total efficiency of denitrification (50.5 ± 3.1 mg N/L) was obtained for carbon source recovery from excess sludge at 70 kJ/L, but the lowest unit cost of nitrogen removal occurred for 140 kJ/L (0.0019 ± 0.0011 EUR/g N).

Yucca Mountain Area Saturated Zone Dissolved Organic Carbon Isotopic Data

International Nuclear Information System (INIS)

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

2007-01-01

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, f ow 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

Characterization and source identification of organic matter in view of land uses and heavy rainfall in the Lake Shihwa, Korea

International Nuclear Information System (INIS)

Lee, Yeonjung; Hur, Jin; Shin, Kyung-Hoon

2014-01-01

Highlights: • Organic matter derived from industrial area showed high biodegradability. • Organic matter transported from rural area was of refractory nature. • Autochthonous organic matter dominated in lake during the dry season. • Contributions of organic source by industrial and rural area increased at rainy season. - Abstract: The characteristics and sources of organic matter in water of the Lake Shihwa, which receives inputs from rural, urban, and industrial areas, were evaluated by examining the biodegradable organic carbon concentration, fluorescence spectra, and carbon and nitrogen isotope ratios, especially during rainy season and dry season. The organic matter transported from rural areas was of refractory nature, while that of industrial origin decomposed rapidly. As compared to the dry season, the organic matter in the rainy season was characterized by a reduced labile fraction. During the dry season, the autochthonous organic matter dominated in the lake, however, the contributions of allochthonous organic sources by industrial and rural areas significantly increased at rainy season. This investigation revealed that the transport of organic matter of anthropogenic origin to the Lake Shihwa was mainly influenced by heavy rainfall. Moreover, each anthropogenic source could differently influence the occurrence of organic matter in water of the Lake Shihwa

Autochthonous and allochthonous contributions of organic carbon to microbial food webs in Svalbard fjords

OpenAIRE

Holding, J.M.; Duarte, C.M.; Delgado-Huertas, A.; Soetaert, K.; Vonk, J.E.; Agusti, S.; Wassmann, P.; Middelburg, J.

2017-01-01

Rising temperatures in the Arctic Ocean are causing sea ice and glaciers to melt at record breaking rates, which has consequences for carbon cycling in the Arctic Ocean that are yet to be fully understood. Microbial carbon cycling is driven by internal processing of in situ produced organic carbon (OC), however recent research suggests that melt water from sea ice and glaciers could introduce an allochthonous source of OC to the microbial food web with ramifications for the metabolic balance ...

Sedimentary organic matter sources, benthic consumption and burial in west Spitsbergen fjords - Signs of maturing of Arctic fjordic systems?

Science.gov (United States)

Zaborska, Agata; Włodarska-Kowalczuk, Maria; Legeżyńska, Joanna; Jankowska, Emilia; Winogradow, Aleksandra; Deja, Kajetan

2018-04-01

Mature ecosystems sequester little organic carbon (Corg) in sediments, as the complex and effective food webs consume most available organic matter within the water column and sediment, in contrast to young systems, where a large proportion of Corg is buried in deeper sediment layers. In this paper we hypothesize that "warmer" Atlantic water influenced fjord exhibits the 'mature' system features as compared to "cooler" Arctic water influenced fjord. Corg concentrations, sources and burial rates, as well as macrobenthic community standing stocks, taxonomic and functional composition and carbon demand, were compared in two west Spitsbergen fjords that are to different extents influenced by Atlantic water and can be treated as representing a cold one (Hornsund) and a warm one (Kongsfjorden). Water, sediments and macrofauna were collected at three stations in the central basin of each fjord. Corg, Ntot, δ13Corg and δ15N were measured in suspended matter, sediment cores and possible organic matter sources. The composition of sources of sedimentary organic matter was modeled by Mix-SIAR Bayesian stable isotope mixing models. The 210Pb method was used to calculate sediment accumulation rates, Corg accumulation and burial rates. The sedimentary Corg concentration and accumulation rate were larger in Hornsund than in Kongsfjorden. The contributions of pelagic sources to the Corg in sediments were similar in both fjords, macroalgal detritus had a higher importance in Kongsfjorden, while terrestrial sources were more important in Hornsund. Similar density and species richness were noted in both fjords, but higher biomass, individual biomass, production and carbon demand of benthic communities were noted in Kongsfjorden despite the lower amounts of Corg in sediments, indicating that macrobenthos responds to quality rather than quantity of available food. Subsurface tube-building conveyer belt detritus feeders (maldanids and oweniids) were responsible for higher standing

Potential Effects of Organic Carbon Production on Ecosystems and Drinking Water Quality

Directory of Open Access Journals (Sweden)

Larry R. Brown

2003-10-01

Full Text Available Restoration of tidal wetlands in the Sacramento-San Joaquin Delta (Delta is an important component of the Ecosystem Restoration Program of the CALFED Bay-Delta Program (CALFED. CALFED is a collaborative effort among state and federal agencies to restore the ecological health and improve water management of the Delta and San Francisco Bay (Bay. Tidal wetland restoration is intended to provide valuable habitat for organisms and to improve ecosystem productivity through export of various forms of organic carbon, including both algae and plant detritus. However, the Delta also provides all or part of the drinking water for over 22 million Californians. In this context, increasing sources of organic carbon may be a problem because of the potential increase in the production of trihalomethanes and other disinfection by-products created during the process of water disinfection. This paper reviews the existing information about the roles of organic carbon in ecosystem function and drinking water quality in the Bay-Delta system, evaluates the potential for interaction, and considers major uncertainties and potential actions to reduce uncertainty. In the last 10 years, substantial progress has been made on the role of various forms of organic carbon in both ecosystem function and drinking water quality; however, interactions between the two have not been directly addressed. Several ongoing studies are beginning to address these interactions, and the results from these studies should reduce uncertainty and provide focus for further research.

Selective enhancement and verification of woody biomass digestibility as a denitrification carbon source.

Science.gov (United States)

Hu, Rongting; Zheng, Xilai; Xin, Jia; Sun, Zhaoyue; Zheng, Tianyuan

2017-11-01

The denitrification efficiency of woody biomass as carbon source is low because of its poor carbon availability. In this study, representative poplar sawdust was pretreated with lime and peracetic acid to enhance the biomass digestibility to different degrees; sawdust was then mixed with soil to investigate its denitrification efficiency. Under controllable conditions (25-95°C, 12-24h, varying dosages), sawdust digestibility (characterized by reducing sugar yield) was selectively enhanced 1.0-21.8 times over that of the raw sawdust (28.8mgeq.glucoseg -1 dry biomass). This increase was mainly attributed to the removal of lignin from the biomass. As a carbon source, the sawdust (digestibility enhanced by 5.4 times) increased the nitrate removal rate by 4.7 times, without N 2 O emission. However, the sawdust with high digestibility (12.6 or 18.0 times), despite releasing more dissolved organic carbon (DOC), did not exhibit further increase in denitrification efficiency, and emitted N 2 O. Copyright © 2017 Elsevier Ltd. All rights reserved.

Microlayer source of oxygenated volatile organic compounds in the summertime marine Arctic boundary layer

Science.gov (United States)

Mungall, Emma L.; Abbatt, Jonathan P. D.; Wentzell, Jeremy J. B.; Lee, Alex K. Y.; Thomas, Jennie L.; Blais, Marjolaine; Gosselin, Michel; Miller, Lisa A.; Papakyriakou, Tim; Willis, Megan D.; Liggio, John

2017-06-01

Summertime Arctic shipboard observations of oxygenated volatile organic compounds (OVOCs) such as organic acids, key precursors of climatically active secondary organic aerosol (SOA), are consistent with a novel source of OVOCs to the marine boundary layer via chemistry at the sea surface microlayer. Although this source has been studied in a laboratory setting, organic acid emissions from the sea surface microlayer have not previously been observed in ambient marine environments. Correlations between measurements of OVOCs, including high levels of formic acid, in the atmosphere (measured by an online high-resolution time-of-flight mass spectrometer) and dissolved organic matter in the ocean point to a marine source for the measured OVOCs. That this source is photomediated is indicated by correlations between the diurnal cycles of the OVOC measurements and solar radiation. In contrast, the OVOCs do not correlate with levels of isoprene, monoterpenes, or dimethyl sulfide. Results from box model calculations are consistent with heterogeneous chemistry as the source of the measured OVOCs. As sea ice retreats and dissolved organic carbon inputs to the Arctic increase, the impact of this source on the summer Arctic atmosphere is likely to increase. Globally, this source should be assessed in other marine environments to quantify its impact on OVOC and SOA burdens in the atmosphere, and ultimately on climate.

Microlayer source of oxygenated volatile organic compounds in the summertime marine Arctic boundary layer.

Science.gov (United States)

Mungall, Emma L; Abbatt, Jonathan P D; Wentzell, Jeremy J B; Lee, Alex K Y; Thomas, Jennie L; Blais, Marjolaine; Gosselin, Michel; Miller, Lisa A; Papakyriakou, Tim; Willis, Megan D; Liggio, John

2017-06-13

Summertime Arctic shipboard observations of oxygenated volatile organic compounds (OVOCs) such as organic acids, key precursors of climatically active secondary organic aerosol (SOA), are consistent with a novel source of OVOCs to the marine boundary layer via chemistry at the sea surface microlayer. Although this source has been studied in a laboratory setting, organic acid emissions from the sea surface microlayer have not previously been observed in ambient marine environments. Correlations between measurements of OVOCs, including high levels of formic acid, in the atmosphere (measured by an online high-resolution time-of-flight mass spectrometer) and dissolved organic matter in the ocean point to a marine source for the measured OVOCs. That this source is photomediated is indicated by correlations between the diurnal cycles of the OVOC measurements and solar radiation. In contrast, the OVOCs do not correlate with levels of isoprene, monoterpenes, or dimethyl sulfide. Results from box model calculations are consistent with heterogeneous chemistry as the source of the measured OVOCs. As sea ice retreats and dissolved organic carbon inputs to the Arctic increase, the impact of this source on the summer Arctic atmosphere is likely to increase. Globally, this source should be assessed in other marine environments to quantify its impact on OVOC and SOA burdens in the atmosphere, and ultimately on climate.

Effect of solids retention time on the bioavailability of organic carbon in anaerobically digested swine waste.

Science.gov (United States)

Kinyua, Maureen N; Cunningham, Jeffrey; Ergas, Sarina J

2014-06-01

Anaerobic digestion (AD) can be used to stabilize and produce energy from livestock waste; however, digester effluents may require further treatment to remove nitrogen. This paper quantifies the effects of varying solids retention time (SRT) methane yield, volatile solids (VS) reduction and organic carbon bioavailability for denitrification during swine waste AD. Four bench-scale anaerobic digesters, with SRTs of 14, 21, 28 and 42 days, operated with swine waste feed. Effluent organic carbon bioavailability was measured using anoxic microcosms and respirometry. Excellent performance was observed for all four digesters, with >60% VS removal and CH4 yields between 0.1 and 0.3(m(3)CH4)/(kg VS added). Organic carbon in the centrate as an internal organic carbon source for denitrification supported maximum specific denitrification rates between 47 and 56(mg NO3(-)-N)/(g VSS h). The digester with the 21-day SRT had the highest CH4 yield and maximum specific denitrification rates. Copyright © 2014 Elsevier Ltd. All rights reserved.

Testing the ``Wildfire Hypothesis:'' Terrestrial Organic Carbon Burning as the Cause of the Paleocene-Eocene Boundary Carbon Isotope Excursion

Science.gov (United States)

Moore, E. A.; Kurtz, A. C.

2005-12-01

The 3‰ negative carbon isotope excursion (CIE) at the Paleocene-Eocene boundary has generally been attributed to dissociation of seafloor methane hydrates. We are testing the alternative hypothesis that the carbon cycle perturbation resulted from wildfires affecting the extensive peatlands and coal swamps formed in the Paleocene. Accounting for the CIE with terrestrial organic carbon rather than methane requires a significantly larger net release of fossil carbon to the ocean-atmosphere, which may be more consistent with the extreme global warming and ocean acidification characteristic of the Paleocene-Eocene Thermal Maximum (PETM). While other researchers have noted evidence of fires at the Paleocene-Eocene boundary in individual locations, the research presented here is designed to test the "wildfire hypothesis" for the Paleocene-Eocene boundary by examining marine sediments for evidence of a global increase in wildfire activity. Such fires would produce massive amounts of soot, widely distributed by wind and well preserved in marine sediments as refractory black carbon. We expect that global wildfires occurring at the Paleocene-Eocene boundary would produce a peak in black carbon abundance at the PETM horizon. We are using the method of Gelinas et al. (2001) to produce high-resolution concentration profiles of black carbon across the Paleocene-Eocene boundary using seafloor sediments from ODP cores, beginning with the Bass River core from ODP leg 174AX and site 1209 from ODP leg 198. This method involves the chemical and thermal extraction of non-refractory carbon followed by combustion of the residual black carbon and measurement as CO2. Measurement of the δ 13C of the black carbon will put additional constraints on the source of the organic material combusted, and will allow us to determine if this organic material was formed prior to or during the CIE.

Organic carbon deliveries and their flow related dynamics in the Fitzroy estuary

International Nuclear Information System (INIS)

Ford, Phillip; Tillman, Pei; Robson, Barbara; Webster, Ian T.

2005-01-01

The Fitzroy estuary (Queensland, Australia) receives large, but highly episodic, river flows from a catchment (144,000 km 2 ) which has undergone major land clearing. Large quantities of suspended sediments, and particulate and dissolved organic carbon are delivered. At peak flows, δ 13 C (-21.7 ± 0.8%o) and C/N (14.8 ± 1.3) of the suspended solids indicate that the particulate organic material entering the estuary is principally soil organic carbon. At the lower beginning flows the particulate organic matter comes from in-stream producers (δ 13 C = -26%o). The DOC load is about 10 times the POC load. Using the inverse method, budgets for POC and DOC were constructed for high and low flows. Under high flows, only a small portion of the POC and DOC load is lost in the estuary. Under dry season (low flow) conditions the estuary is a sink for DOC, but remains a source of POC to the coastal waters

Made-to-order metal-organic frameworks for trace carbon dioxide removal and air capture

KAUST Repository

Shekhah, Osama

2014-06-25

Direct air capture is regarded as a plausible alternate approach that, if economically practical, can mitigate the increasing carbon dioxide emissions associated with two of the main carbon polluting sources, namely stationary power plants and transportation. Here we show that metal-organic framework crystal chemistry permits the construction of an isostructural metal-organic framework (SIFSIX-3-Cu) based on pyrazine/copper(II) two-dimensional periodic 4 4 square grids pillared by silicon hexafluoride anions and thus allows further contraction of the pore system to 3.5 versus 3.84 for the parent zinc(II) derivative. This enhances the adsorption energetics and subsequently displays carbon dioxide uptake and selectivity at very low partial pressures relevant to air capture and trace carbon dioxide removal. The resultant SIFSIX-3-Cu exhibits uniformly distributed adsorption energetics and offers enhanced carbon dioxide physical adsorption properties, uptake and selectivity in highly diluted gas streams, a performance, to the best of our knowledge, unachievable with other classes of porous materials. 2014 Macmillan Publishers Limited.

Deposition and benthic mineralization of organic carbon

DEFF Research Database (Denmark)

Nordi, Gunnvor A.; Glud, Ronnie N.; Simonsen, Knud

2018-01-01

Seasonal variations in sedimentation and benthic mineralization of organic carbon (OC) were investigated in a Faroese fjord. Deposited particulate organic carbon (POC) was mainly of marine origin, with terrestrial material only accounting for b1%. On an annual basis the POC export fromthe euphotic...

Differences in temperature, organic carbon and oxygen consumption among lowland streams

DEFF Research Database (Denmark)

Sand-Jensen, K.; Pedersen, N. L.

2005-01-01

1. Temperature, organic carbon and oxygen consumption were measured over a year at 13 sites in four lowlands streams within the same region in North Zealand, Denmark with the objectives of determining: (i) spatial and seasonal differences between open streams, forest streams and streams with or w......1. Temperature, organic carbon and oxygen consumption were measured over a year at 13 sites in four lowlands streams within the same region in North Zealand, Denmark with the objectives of determining: (i) spatial and seasonal differences between open streams, forest streams and streams...... the exponential increase of oxygen consumption rate between 4 and 20 °C averaged 0.121 °C-1 (Q10 of 3.35) in 70 measurements and showed no significant variations between seasons and stream sites or correlations with ambient temperature and organic content. 5. Oxygen consumption rate was enhanced downstream...... at ambient temperature by 30-40% and 80-130%, respectively. Faster consumption of organic matter and dissolved oxygen downstream of point sources should increase the likelihood of oxygen stress of the stream biota and lead to the export of less organic matter but more mineralised nutrients to the coastal...

Carbon isotopes and lipid biomarker investigation of sources, transport and degradation of terrestrial organic matter in the Buor-Khaya Bay, SE Laptev Sea

Directory of Open Access Journals (Sweden)

E. S. Karlsson

2011-07-01

Full Text Available The world's largest continental shelf, the East Siberian Shelf Sea, receives substantial input of terrestrial organic carbon (terr-OC from both large rivers and erosion of its coastline. Degradation of organic matter from thawing permafrost in the Arctic is likely to increase, potentially creating a positive feedback mechanism to climate warming. This study focuses on the Buor-Khaya Bay (SE Laptev Sea, an area with strong terr-OC input from both coastal erosion and the Lena river. To better understand the fate of this terr-OC, molecular (acyl lipid biomarkers and isotopic tools (stable carbon and radiocarbon isotopes have been applied to both particulate organic carbon (POC in surface water and sedimentary organic carbon (SOC collected from the underlying surface sediments.

Clear gradients in both extent of degradation and differences in source contributions were observed both between surface water POC and surface sediment SOC as well as over the 100 s km investigation scale (about 20 stations. Depleted δ¹³C-OC and high HMW/LMW n-alkane ratios signaled that terr-OC was dominating over marine/planktonic sources.

Despite a shallow water column (10–40 m, the isotopic shift between SOC and POC varied systematically from +2 to +5 per mil for δ¹³C and from +300 to +450 for Δ¹⁴C from the Lena prodelta to the Buor-Khaya Cape. At the same time, the ratio of HMW n-alkanoic acids to HMW n-alkanes as well as HMW n-alkane CPI, both indicative of degradation, were 5–6 times greater in SOC than in POC. This suggests that terr-OC was substantially older yet less degraded in the surface sediment than in the surface waters. This unusual vertical degradation trend was only recently found also for the central East Siberian Sea.

Numerical modeling (Monte Carlo simulations with δ¹³C and Δ¹⁴C in both POC and SOC was applied to deduce the relative

Fluvial organic carbon losses from oil palm plantations on tropical peat, Sarawak, Southeast Asia

Science.gov (United States)

Cook, Sarah; Page, Susan; Evans, Chris; Whelan, Mick; Gauci, Vincent; Lip Khoon, Kho

2017-04-01

Tropical peatlands are valuable stores of carbon. However, tropical peat swamp forests (TPSFs) in Southeast Asia have increasingly been converted to other land-uses. For example, more than 25% of TPSFs are now under oil palm plantations. This conversion - requiring felling and burning of trees and drainage of the peat - can enhance carbon mineralization, dissolved organic carbon (DOC) losses and can contribute significantly to global anthropogenic greenhouse gas emissions, changing these natural carbon sinks into carbon sources. At present, relatively few scientifically sound studies provide dependable estimates of gaseous and fluvial carbon losses from oil palm plantations or from drained tropical peat in general. Here we present an annual (54 week) estimate of the export of dissolved and particulate organic carbon in water draining two oil palm estates and nearby stands of TPSF in Sarawak, Malaysia, subjected to varying degrees of past anthropogenic disturbance. Spectrophotometric techniques including SUVA254 (Specific Ultra-Violet Absorption) were used to gain insight into the aromaticity and subsequent bioavailability of the exported DOC. Water draining plantation and deforested land had a higher proportion of labile carbon compared to water draining forested areas. Preliminary data suggest a total fluvial DOC flux from plantations of ca. 190 g C m-2 year-1; nearly three times estimates from intact TPSFs (63 g C m-2 year-1). DOC accounted for between 86 % - 94 % of the total organic carbon lost (most of which was bioavailable). Wit et al. (2015) estimates that an average of 53 % of peat-derived DOC is decomposed and emitted as CO2, on a monthly basis. Based on these estimates our data suggests an additional 101 g CO2 m-2 may be emitted indirectly from fluvial organic carbon in degraded TPSFs per year. Overall, these findings emphasize the importance of including fluvial organic carbon fluxes when quantifying the impact of anthropogenic disturbance on the

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

International Nuclear Information System (INIS)

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 CO 2 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

Hidden cycle of dissolved organic carbon in the deep ocean.

Science.gov (United States)

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

2014-11-25

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 δ(13)C and age via Δ(14)C. 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.

Achieving high performance in intermediate temperature direct carbon fuel cells with renewable carbon as a fuel source

International Nuclear Information System (INIS)

Hao, Wenbin; He, Xiaojin; Mi, Yongli

2014-01-01

Highlights: • Bamboo fiber and waste paper were pyrolyzed to generate bamboo carbon and waste paper carbon as anode fuels of IT-DCFC. • Superior cell performance was achieved with the waste paper carbon. • The results suggested the high performance was due to the highest thermal reactivity and the catalytic inherent impurities. • Calcite and kaolinite as inherent impurities favored the thermal decomposition and the electrooxidation of carbon. - Abstract: Three kinds of carbon sources obtained from carbon black, bamboo fiber and waste paper were investigated as anode fuels in an intermediate temperature direct carbon fuel cell. The carbon sources were characterized with X-ray photoelectron spectroscopy, thermal gravimetric analysis, etc. The results indicated that the waste paper carbon was more abundant in calcite and kaolinite, and showed higher thermal reactivity in the intermediate temperature range compared with the other two carbon sources. The cell performance was tested at 650 °C in a hybrid single cell, using Sm 0.20 Ce 0.80 O 2−x as the electrolyte. As a result, the cell fed with waste paper carbon showed the highest performance among the three carbon sources, with a peak power density of 225 mW cm −2 . The results indicated that its inherent impurities, such as calcite and kaolinite, might favor the thermal gasification of renewable carbon sources, which resulted in the enhanced performance of the intermediate temperature direct carbon fuel cell

Organic carbon isotope systematics of coastal marshes

NARCIS (Netherlands)

Middelburg, J.J.; Nieuwenhuize, J.; Lubberts, R.K.; Van de Plassche, O.

1997-01-01

Measurements of nitrogen, organic carbon and delta(13)C are presented for Spartina-dominated marsh sediments from a mineral marsh in SW Netherlands and from a peaty marsh in Massachusetts, U.S.A. delta(13)C Of organic carbon in the peaty marsh sediments is similar to that of Spartina material,

Growth of graphene films from non-gaseous carbon sources

Science.gov (United States)

Tour, James; Sun, Zhengzong; Yan, Zheng; Ruan, Gedeng; Peng, Zhiwei

2015-08-04

In various embodiments, the present disclosure provides methods of forming graphene films by: (1) depositing a non-gaseous carbon source onto a catalyst surface; (2) exposing the non-gaseous carbon source to at least one gas with a flow rate; and (3) initiating the conversion of the non-gaseous carbon source to the graphene film, where the thickness of the graphene film is controllable by the gas flow rate. Additional embodiments of the present disclosure pertain to graphene films made in accordance with the methods of the present disclosure.

[Effects of Chinese prickly ash orchard on soil organic carbon mineralization and labile organic carbon in karst rocky desertification region of Guizhou province].

Science.gov (United States)

Zhang, Wen-Juan; Liao, Hong-Kai; Long, Jian; Li, Juan; Liu, Ling-Fei

2015-03-01

Taking 5-year-old Chinese prickly ash orchard (PO-5), 17-year-old Chinese prickly ash orchard (PO- 17), 30-year-old Chinese prickly ash orchard (PO-30) and the forest land (FL, about 60 years) in typical demonstration area of desertification control test in southwestern Guizhou as our research objects, the aim of this study using a batch incubation experiment was to research the mineralization characteristics of soil organic carbon and changes of the labile soil organic carbon contents at different depths (0-15 cm, 15-30 cm, and 30-50 cm). The results showed that: the cumulative mineralization amounts of soil organic carbon were in the order of 30-year-old Chinese prickly ash orchard, the forest land, 5-year-old Chinese prickly ash orchard and 17-year-old Chinese prickly ash orchard at corresponding depth. Distribution ratios of CO2-C cumulative mineralization amount to SOC contents were higher in Chinese prickly ash orchards than in forest land at each depth. Cultivation of Chinese prickly ash in long-term enhanced the mineralization of soil organic carbon, and decreased the stability of soil organic carbon. Readily oxidized carbon and particulate organic carbon in forest land soils were significantly more than those in Chinese prickly ash orchards at each depth (P < 0.05). With the increasing times of cultivation of Chinese prickly ash, the contents of readily oxidized carbon and particulate organic carbon first increased and then declined at 0-15 cm and 15-30 cm depth, respectively, but an opposite trend was found at 30-50 cm depth. At 0-15 cm and 15-30 cm, cultivation of Chinese prickly ash could be good for improving the contents of labile soil organic carbon in short term, but it was not conducive in long-term. In this study, we found that cultivation of Chinese prickly ash was beneficial for the accumulation of labile organic carbon at the 30-50 cm depth.

Organic compounds in aerosols from selected European sites - Biogenic versus anthropogenic sources

Science.gov (United States)

Alves, Célia; Vicente, Ana; Pio, Casimiro; Kiss, Gyula; Hoffer, Andras; Decesari, Stefano; Prevôt, André S. H.; Minguillón, María Cruz; Querol, Xavier; Hillamo, Risto; Spindler, Gerald; Swietlicki, Erik

2012-11-01

Atmospheric aerosol samples from a boreal forest (Hyytiälä, April 2007), a rural site in Hungary (K-puszta, summer 2008), a polluted rural area in Italy (San Pietro Capofiume, Po Valley, April 2008), a moderately polluted rural site in Germany located on a meadow (Melpitz, May 2008), a natural park in Spain (Montseny, March 2009) and two urban background locations (Zurich, December 2008, and Barcelona, February/March 2009) were collected. Aliphatics, polycyclic aromatic hydrocarbons, carbonyls, sterols, n-alkanols, acids, phenolic compounds and anhydrosugars in aerosols were chemically characterised by gas chromatography-mass spectrometry, along with source attribution based on the carbon preference index (CPI), the ratios between the unresolved and the chromatographically resolved aliphatics, the contribution of wax n-alkanes, n-alkanols and n-alkanoic acids from plants, diagnostic ratios of individual target compounds and source-specific markers to organic carbon ratios. In spite of transboundary pollution episodes, Hyytiälä registered the lowest levels among all locations. CPI values close to 1 for the aliphatic fraction of the Montseny aerosol suggest that the anthropogenic input may be associated with the transport of aged air masses from the surrounding industrial/urban areas, which superimpose the locally originated hydrocarbons with biogenic origin. Aliphatic and aromatic hydrocarbons in samples from San Pietro Capofiume reveal that fossil fuel combustion is a major source influencing the diel pattern of concentrations. This source contributed to 25-45% of the ambient organic carbon (OC) at the Po Valley site. Aerosols from the German meadow presented variable contributions from both biogenic and anthropogenic sources. The highest levels of vegetation wax components and biogenic secondary organic aerosol (SOA) products were observed at K-puszta, while anthropogenic SOA compounds predominated in Barcelona. The primary vehicular emissions in the Spanish

Autochthonous and allochthonous contributions of organic carbon to microbial food webs in Svalbard fjords

KAUST Repository

Holding, Johnna M.; Duarte, Carlos M.; Delgado-Huertas, Antonio; Soetaert, Karline; Vonk, Jorien E.; Agusti, Susana; Wassmann, Paul; Middelburg, Jack J.

2017-01-01

Rising temperatures in the Arctic Ocean are causing sea ice and glaciers to melt at record breaking rates, which has consequences for carbon cycling in the Arctic Ocean that are yet to be fully understood. Microbial carbon cycling is driven by internal processing of in situ produced organic carbon (OC), however recent research suggests that melt water from sea ice and glaciers could introduce an allochthonous source of OC to the microbial food web with ramifications for the metabolic balance of plankton communities. In this study, we characterized autochthonous and allochthonous sources of OC to the Western Svalbard fjord system using stable isotopes of carbon. We quantified δ13C of eukaryotic and prokaryotic planktonic groups using polar lipid-derived fatty acids as biomarkers in addition to measuring δ13C of marine particulate OC and dissolved OC from glacial runoff. δ13C of bacteria (−22.5‰) was higher than that of glacial runoff OC (−28.5‰) and other phytoplankton groups (−24.7 to −29.1‰), which suggests that marine bacteria preferentially use a third source of OC. We present a Bayesian three-source δ13C mixing model whereby ∼ 60% of bacteria carbon is derived from OC in sea ice, and the remaining carbon is derived from autochthonous production and glacial-derived OC. These results suggest that subsidies of OC from melting glaciers will not likely influence microbial carbon cycling in Svalbard fjords in the future and that further research is needed to determine the effects of melting sea ice on microbial carbon cycling in fjord systems and elsewhere in the Arctic Ocean.

Autochthonous and allochthonous contributions of organic carbon to microbial food webs in Svalbard fjords

KAUST Repository

Holding, Johnna M.

2017-03-27

Rising temperatures in the Arctic Ocean are causing sea ice and glaciers to melt at record breaking rates, which has consequences for carbon cycling in the Arctic Ocean that are yet to be fully understood. Microbial carbon cycling is driven by internal processing of in situ produced organic carbon (OC), however recent research suggests that melt water from sea ice and glaciers could introduce an allochthonous source of OC to the microbial food web with ramifications for the metabolic balance of plankton communities. In this study, we characterized autochthonous and allochthonous sources of OC to the Western Svalbard fjord system using stable isotopes of carbon. We quantified δ13C of eukaryotic and prokaryotic planktonic groups using polar lipid-derived fatty acids as biomarkers in addition to measuring δ13C of marine particulate OC and dissolved OC from glacial runoff. δ13C of bacteria (−22.5‰) was higher than that of glacial runoff OC (−28.5‰) and other phytoplankton groups (−24.7 to −29.1‰), which suggests that marine bacteria preferentially use a third source of OC. We present a Bayesian three-source δ13C mixing model whereby ∼ 60% of bacteria carbon is derived from OC in sea ice, and the remaining carbon is derived from autochthonous production and glacial-derived OC. These results suggest that subsidies of OC from melting glaciers will not likely influence microbial carbon cycling in Svalbard fjords in the future and that further research is needed to determine the effects of melting sea ice on microbial carbon cycling in fjord systems and elsewhere in the Arctic Ocean.

Soil organic carbon assessments in cropping systems using isotopic techniques

Science.gov (United States)

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, is probably due to the presence of deep roots under pastures in ICLS. Delta carbon-13 values for 0-5 cm were -22.9, -21.2 and -19.9 per mil for REF, ICLS and CCS, respectively (Pis explained by the presence of tree species with high lignin content in natural vegetation. Lignin has lower delta carbon-13 compared to cellulose (dominating in crops and pastures), which is present in greater proportion in plant residues of

Large contribution of fossil fuel derived secondary organic carbon to water soluble organic aerosols in winter haze in China

Directory of Open Access Journals (Sweden)

Y.-L. Zhang

2018-03-01

Full Text Available Water-soluble organic carbon (WSOC is a large fraction of organic aerosols (OA globally and has significant impacts on climate and human health. The sources of WSOC remain very uncertain in polluted regions. Here we present a quantitative source apportionment of WSOC, isolated from aerosols in China using radiocarbon (14C and offline high-resolution time-of-flight aerosol mass spectrometer measurements. Fossil emissions on average accounted for 32–47 % of WSOC. Secondary organic carbon (SOC dominated both the non-fossil and fossil derived WSOC, highlighting the importance of secondary formation to WSOC in severe winter haze episodes. Contributions from fossil emissions to SOC were 61 ± 4 and 50 ± 9 % in Shanghai and Beijing, respectively, significantly larger than those in Guangzhou (36 ± 9 % and Xi'an (26 ± 9 %. The most important primary sources were biomass burning emissions, contributing 17–26 % of WSOC. The remaining primary sources such as coal combustion, cooking and traffic were generally very small but not negligible contributors, as coal combustion contribution could exceed 10 %. Taken together with earlier 14C source apportionment studies in urban, rural, semi-urban and background regions in Asia, Europe and the USA, we demonstrated a dominant contribution of non-fossil emissions (i.e., 75 ± 11 % to WSOC aerosols in the Northern Hemisphere; however, the fossil fraction is substantially larger in aerosols from East Asia and the eastern Asian pollution outflow, especially during winter, due to increasing coal combustion. Inclusion of our findings can improve a modelling of effects of WSOC aerosols on climate, atmospheric chemistry and public health.

Carbonate stable isotope constraints on sources of arsenic contamination in Neogene tufas and travertines of Attica, Greece

Science.gov (United States)

Kampouroglou, Evdokia E.; Tsikos, Harilaos; Economou-Eliopoulos, Maria

2017-11-01

We presented new C and O isotope data of rockforming calcite in terrestrial carbonate deposits from Neogene basins of Attica (Greece), coupled with standard mineralogical and bulk geochemical results. Whereas both isotope datasets [δ18O from -8.99 to -3.20‰(VPDB); δ13C from -8.17 to +1.40‰(VPDB)] could be interpreted in principle as indicative of a meteoric origin, the clear lack of a statistical correlation between them suggests diverse sources for the isotopic variation of the two elements. On the basis of broad correlations between lower carbon isotope data with increasing Fe and bulk organic carbon, we interpreted the light carbon isotope signatures and As enrichments as both derived mainly from a depositional process involving increased supply of metals and organic carbon to the original basins. Periodically augmented biological production and aerobic cycling of organic matter in the ambient lake waters, would have led to the precipitation of isotopically light calcite in concert with elevated fluxes of As-bearing iron oxy-hydroxide and organic matter to the initial terrestrial carbonate sediment. The terrestrial carbonate deposits of Attica therefore represented effective secondary storage reservoirs of elevated As from the adjacent mineralized hinterland; hence these and similar deposits in the region ought to be regarded as key geological candidates for anomalous supply of As to local soils, groundwater and related human activities.

Volatile organic carbon/air separation test using gas membranes

International Nuclear Information System (INIS)

King, C.V.; Kaschemekat, J.

1993-08-01

An estimated 900 metric tons of carbon tetrachloride were discharged to soil columns during the Plutonium Finishing Plant Operations at the Hanford Site. The largest percentage of this volatile organic compound was found in the vadose region of the 200 West Area. Using a Vacuum Extraction System, the volatile organic compound was drawn from the soil in an air mixture at a concentration of about 1,000 parts per million. The volatile organic compounds were absorbed from the air stream using granulated activated carbon canisters. A gas membrane separation system, developed by Membrane Technology and Research, Inc., was tested at the Vacuum Extraction System site to determine if the volatile organic compound load on the granulated activated carbon could be reduced. The Vacuum Extraction System condensed most of the volatile organic compound into liquid carbon tetrachloride and vented the residual gas stream into the granulated activated carbon. This system reduced the cost of operation about $5/kilogram of volatile organic compound removed

The potential of carbon and nitrogen isotopes to conservatively discriminate between subsoil sediment sources

Science.gov (United States)

Laceby, J. Patrick; Olley, Jon

2013-04-01

Moreton Bay, in South East Queensland, Australia, is a Ramsar wetland of international significance. A decline of the bay's ecosystem health has been primarily attributed to sediments and nutrients from catchment sources. Sediment budgets for three catchments indicated gully erosion dominates the supply of sediment in Knapp Creek and the Upper Bremer River whereas erosion from cultivated soils is the primary sediment source in Blackfellow Creek. Sediment tracing with fallout-radionuclides confirmed subsoil erosion processes dominate the supply of sediment in Knapp Creek and the Upper Bremer River whereas in Blackfellow Creek cultivated and subsoil sources contribute >90% of sediments. Other sediment properties are required to determine the relative sediment contributions of channel bank, gully and cultivated sources in these catchments. The potential of total organic carbon (TOC), total nitrogen (TN), and carbon and nitrogen stable isotopes (δ13C, δ15N) to conservatively discriminate between subsoil sediment sources is presented. The conservativeness of these sediment properties was examined through evaluating particle size variations in depth core soil samples and investigating whether they remain constant in source soils over two sampling occasions. Varying conservative behavior and source discrimination was observed. TN in the

Radiocarbon measurements of dissolved organic carbon in sewage-treatment-plant effluent and domestic sewage

International Nuclear Information System (INIS)

Nara, Fumiko Watanabe; Imai, Akio; Matsushige, Kazuo; Komatsu, Kazuhiro; Kawasaki, Nobuyuki; Shibata, Yasuyuki

2010-01-01

In an attempt to better characterize dissolved organic carbon (DOC) in several specific sources to Lake Kasumigaura, such as sewage-treatment-plant effluent (STPE), domestic sewage (DS) and forest stream (FS), we analyzed radiocarbon ( 14 C) and stable carbon isotopic compositions ( 13 C) of the DOCs. The measurements of 14 C for DOC were performed by an accelerator mass spectrometer (AMS) at the National Institute for Environmental Studies (NIES-TERRA) in Japan. The Δ 14 C and δ 13 C values of the DOCs in several sources to Lake Kasumigaura, have low carbon isotopic values, ranging from -470 per mille to -79 per mille and from -27.9 per mille to -24.2 per mille , respectively. These carbon isotopic values are substantially different from those of Lake Kasumigaura. These results imply different origins for the DOC in Lake Kasumigaura. The 14 C and 13 C analyses of DOC led to a useful classification for DOCs in Lake Kasumigaura, Japan.

Dissolved organic carbon ameliorates the effects of UV radiation on a freshwater fish

Energy Technology Data Exchange (ETDEWEB)

Manek, Aditya K., E-mail: aditya.manek@usask.ca [Department of Biology, University of Saskatchewan, Saskatoon, S7N 5E2 SK (Canada); Ferrari, Maud C.O. [Department of Biomedical Sciences, WCVM, University of Saskatchewan, Saskatoon, S7N 5B4 SK (Canada); Chivers, Douglas P.; Niyogi, Som [Department of Biology, University of Saskatchewan, Saskatoon, S7N 5E2 SK (Canada)

2014-08-15

Anthropogenic activities over the past several decades have depleted stratospheric ozone, resulting in a global increase in ultraviolet radiation (UVR). Much of the negative effects of UVR in aquatic systems is minimized by dissolved organic carbon (DOC) which is known to attenuate UVR across the water column. The skin of many fishes contains large epidermal club cells (ECCs) that are known to play a role in innate immune responses and also release chemical alarm cues that warn other fishes of danger. This study investigated the effects of in vivo UVR exposure to fathead minnows (Pimephales promelas), under the influence of two sources of DOC: Sigma Aldrich humic acid, a coal based commercial source of DOC and Luther Marsh natural organic matter, a terrigenous source of DOC. Specifically, we examined ECC investment and physiological stress responses and found that fish exposed to high UVR, in the presence of either source of DOC, had higher ECC investment than fish exposed to high UVR only. Similarly, exposure to high UVR under either source of DOC, reduced cortisol levels relative to that in the high UVR only treatment. This indicates that DOC protects fish from physiological stress associated with UVR exposure and helps maintain production of ECC under conditions of UVR exposure. - Highlights: • We examined the combined effect of UV radiation and Dissolved Organic Carbon on fish. • Physiological stress response and epidermal club cell investment were measured. • Fish exposed to high UVR and DOC had higher ECC investment and reduced cortisol levels. • DOC plays a role in protecting fish from physiological stress and maintains ECC production.

Dissolved organic carbon ameliorates the effects of UV radiation on a freshwater fish

International Nuclear Information System (INIS)

Manek, Aditya K.; Ferrari, Maud C.O.; Chivers, Douglas P.; Niyogi, Som

2014-01-01

Anthropogenic activities over the past several decades have depleted stratospheric ozone, resulting in a global increase in ultraviolet radiation (UVR). Much of the negative effects of UVR in aquatic systems is minimized by dissolved organic carbon (DOC) which is known to attenuate UVR across the water column. The skin of many fishes contains large epidermal club cells (ECCs) that are known to play a role in innate immune responses and also release chemical alarm cues that warn other fishes of danger. This study investigated the effects of in vivo UVR exposure to fathead minnows (Pimephales promelas), under the influence of two sources of DOC: Sigma Aldrich humic acid, a coal based commercial source of DOC and Luther Marsh natural organic matter, a terrigenous source of DOC. Specifically, we examined ECC investment and physiological stress responses and found that fish exposed to high UVR, in the presence of either source of DOC, had higher ECC investment than fish exposed to high UVR only. Similarly, exposure to high UVR under either source of DOC, reduced cortisol levels relative to that in the high UVR only treatment. This indicates that DOC protects fish from physiological stress associated with UVR exposure and helps maintain production of ECC under conditions of UVR exposure. - Highlights: • We examined the combined effect of UV radiation and Dissolved Organic Carbon on fish. • Physiological stress response and epidermal club cell investment were measured. • Fish exposed to high UVR and DOC had higher ECC investment and reduced cortisol levels. • DOC plays a role in protecting fish from physiological stress and maintains ECC production

Carbon source feeding strategies for recombinant protein ...

African Journals Online (AJOL)

USER

2010-04-12

Apr 12, 2010 ... protein expression with the influence of the carbon source feeding ... in the culture media, increasing the peroxisomes numbers ...... source, temperature, pH, O2, methanol feeding strategy) ..... Catabolite Inactivation in Yeast.

Sources and fate of organic matter in suspended and bottom sediments of the Mandovi and Zuari estuaries, Western India

Digital Repository Service at National Institute of Oceanography (India)

Shynu, R; Rao, V.P.; Sarma, V.V.S.S.; Kessarkar, P.M.; ManiMurali, R

in western India during wet and dry seasons, to characterize the sources of organic matter (OM) in these systems. Unlike major rivers, SPM concentrations increase seaward with a general trend of decreasing particulate organic carbon (POC) in these rivers...

234Th as tracer of organic carbon export in Bransfield Strait, Antarctic

International Nuclear Information System (INIS)

Oliveira, Joselene de; Vieira, Lucia Helena; Duarte, Celina Lopes

2011-01-01

The element thorium has multiple isotopes that have emerged collectively as a powerful set of tracers for particle associated processes in the oceans. The production of 2 34T h from 2 38U , coupled with the conservative behavior of 2 38U in seawater, makes the source of 2 34T h easy to characterize. Because of its very particle reactive behavior, 2 34T h is removed from a parcel of water in only two ways, through decay and through particle flux. Therefore, a steady-state 1D activity balance can be used to calculate its flux. This work presents results of a collaborative research on organic carbon fluxes distribution in the Bransfield Strait. Macro-nutrients, micro nutrients and chlorophyll-a distributions were used to examine the pathway sources. 2 34T h was used as a tracer of organic carbon fluxes distribution in the Bransfield Strait in order to evaluate its influence in the CO 2 drawdown, since POC export via sinking particles is the primary mechanism of carbon sequestration in the Southern Ocean. Fluxes up to 15274 dmp m-2 d-1 were estimated, the highest value observed in Station 09 at 794 m depth. POC exported fluxes derived from the disequilibrium 2 34T h/ 2 38U model varied from 0.6 to 16000 mmol C m -2 d -1 . (author)

Elucidating Adsorptive Fractions of Natural Organic Matter on Carbon Nanotubes.

Science.gov (United States)

Ateia, Mohamed; Apul, Onur G; Shimizu, Yuta; Muflihah, Astri; Yoshimura, Chihiro; Karanfil, Tanju

2017-06-20

Natural organic matter (NOM) is a heterogeneous mixture of organic compounds that is omnipresent in natural waters. To date, the understanding of the adsorption of NOM components by carbon nanotubes (CNTs) is limited because of the limited number of comprehensive studies in the literature examining the adsorption of NOM by CNTs. In this study, 11 standard NOM samples from various sources were characterized, and their adsorption behaviors on four different CNTs were examined side-by-side using total organic carbon, fluorescence, UV-visible spectroscopy, and high-performance size-exclusion chromatography (HPSEC) analysis. Adsorption was influenced by the chemical properties of the NOM, including aromaticity, degree of oxidation, and carboxylic acidity. Fluorescence excitation-emission matrix (EEM) analysis showed preferential adsorption of decomposed and terrestrial-derived NOM compared to freshly produced and microbial-derived NOM. HPSEC analysis revealed preferential adsorption of fractions in the molecular weight range of 0.5-2 kDa for humic acids but in the molecular weight range of 1-3 kDa for all fulvic acids and reverse-osmosis isolates. However, the smallest characterized fraction (MW < 0.4 kDa) in all samples did not adsorb on the CNTs.

Total observed organic carbon (TOOC in the atmosphere: a synthesis of North American observations

Directory of Open Access Journals (Sweden)

C. L. Heald

2008-04-01

Full Text Available Measurements of organic carbon compounds in both the gas and particle phases made upwind, over and downwind of North America are synthesized to examine the total observed organic carbon (TOOC in the atmosphere over this region. These include measurements made aboard the NOAA WP-3 and BAe-146 aircraft, the NOAA research vessel Ronald H. Brown, and at the Thompson Farm and Chebogue Point surface sites during the summer 2004 ICARTT campaign. Both winter and summer 2002 measurements during the Pittsburgh Air Quality Study are also included. Lastly, the spring 2002 observations at Trinidad Head, CA, surface measurements made in March 2006 in Mexico City and coincidentally aboard the C-130 aircraft during the MILAGRO campaign and later during the IMPEX campaign off the northwestern United States are incorporated. Concentrations of TOOC in these datasets span more than two orders of magnitude. The daytime mean TOOC ranges from 4.0 to 456 μgC m⁻³ from the cleanest site (Trinidad Head to the most polluted (Mexico City. Organic aerosol makes up 3–17% of this mean TOOC, with highest fractions reported over the northeastern United States, where organic aerosol can comprise up to 50% of TOOC. Carbon monoxide concentrations explain 46 to 86% of the variability in TOOC, with highest TOOC/CO slopes in regions with fresh anthropogenic influence, where we also expect the highest degree of mass closure for TOOC. Correlation with isoprene, formaldehyde, methyl vinyl ketone and methacrolein also indicates that biogenic activity contributes substantially to the variability of TOOC, yet these tracers of biogenic oxidation sources do not explain the variability in organic aerosol observed over North America. We highlight the critical need to develop measurement techniques to routinely detect total gas phase VOCs, and to deploy comprehensive suites of TOOC instruments in diverse environments to quantify the ambient evolution of organic carbon from source

Radiocarbon and stable carbon isotope compositions of chemically fractionated soil organic matter in a temperate-zone forest

International Nuclear Information System (INIS)

Koarashi, Jun; Iida, Takao; Asano, Tomohiro

2005-01-01

To better understand the role of soil organic matter in terrestrial carbon cycle, carbon isotope compositions in soil samples from a temperate-zone forest were measured for bulk, acid-insoluble and base-insoluble organic matter fractions separated by a chemical fractionation method. The measurements also made it possible to estimate indirectly radiocarbon ( 14 C) abundances of acid- and base-soluble organic matter fractions, through a mass balance of carbon among the fractions. The depth profiles of 14 C abundances showed that (1) bomb-derived 14 C has penetrated the first 16 cm mineral soil at least; (2) Δ 14 C values of acid-soluble organic matter fraction are considerably higher than those of other fractions; and (3) a significant amount of the bomb-derived 14 C has been preserved as the base-soluble organic matter around litter-mineral soil boundary. In contrast, no or little bomb-derived 14 C was observed for the base-insoluble fraction in all sampling depths, indicating that this recalcitrant fraction, accounting for approximately 15% of total carbon in this temperate-zone forest soil, plays a role as a long-term sink in the carbon cycle. These results suggest that bulk soil organic matter cannot provide a representative indicator as a source or a sink of carbon in soil, particularly on annual to decadal timescales

Organic carbon isotope ratios of recent sediments from coastal lagoons of the Gulf of Mexico, Mexico

International Nuclear Information System (INIS)

Botello, A.V.; Mandelli, E.F.; Macko, S.; Parker, P.L.

1980-01-01

The stable carbon isotope composition of sedimentary organic carbon was determined in the sediments of seven coastal lagoons of the Gulf of Mexico, Mexico. For most of the lagoons the delta 13 C values for sediments ranged from -20.1 to -23.9 parts per thousand. Anomalously low values, -26.8 to 29.3 parts per thousand were determined in sediments of two of the studied lagoons, probably due to the presence of organic carbon from anthropogenic sources, naturally absent in these environments. The delta 13 C values determined in the tissues of oysters collected at the same time in the different lagoons were very similar to those recorded in the sediments. (author)

Barrow Black Carbon Source and Impact Study Final Campaign Report

Energy Technology Data Exchange (ETDEWEB)

Barrett, Tate [Baylor Univ., Waco, TX (United States)

2014-07-01

The goal of the Barrow Black Carbon Source and Impact (BBCSI) Study was to characterize the concentration and isotopic composition of carbonaceous atmospheric particulate matter (PM) at the Atmospheric Radiation Measurement site in Barrow, AK. The carbonaceous component was characterized via measurement of the organic and black carbon (OC and BC) components of the total PM. To facilitate complete characterization of the particulate matter, filter-based collections were used, including a medium volume PM2.5 sampler and a high volume PM10 sampler. Thirty-eight fine (PM2.5) and 49 coarse (PM10) particulate matter fractions were collected at weekly and bi-monthly intervals. The PM2.5 sampler operated with minimal maintenance during the 12 month campaign. The PM10 sampler used for the BBCSI used standard Tisch hi-vol motors which have a known lifetime of ~1 month under constant use; this necessitated monthly maintenance and it is suggested that the motors be upgraded to industrial blowers for future deployment in the Arctic. The BBCSI sampling campaign successfully collected and archived 87 ambient atmospheric particulate matter samples from Barrow, AK from July 2012 to June 2013. Preliminary analysis of the organic and black carbon concentrations has been completed. This campaign confirmed known trends of high BC lasting from the winter through to spring haze periods and low BC concentrations in the summer.

Carbon trading and carbon taxation: how to consider biotic sources and sinks

International Nuclear Information System (INIS)

Madlener, Reinhard; Schlamadinger, Bernhard

1999-01-01

The Kyoto Protocol (KP) to the UNFCCC includes land-use change and forestry in the carbon accounting process, limited to afforestation, reforestation and deforestation since 1990, and explicitly provides for the option of using a variety of flexibility mechanisms to meet the greenhouse gas (GHG) reduction targets stipulated in a more cost-efficient manner. Domestically, different countries might adopt different approaches to achieve their emission reduction objectives, such as carbon trading or carbon taxation, and it is not clear to date what the implications for bioenergy use, forestry, and land-use change can be expected to be. With respect to national GHG emissions trading, the main issues studied in this paper are: Should trading of fossil fuel emissions allowances be coupled with trading of biotic credits and debits? Should credits for carbon sequestration in forests be auctioned or grandfathered? Should there be a distinction between a carbon permit issued for an additional biotic sink and those issued for fossil fuel carbon emissions? Is there a difference for biotic carbon sinks and sources between one-time permits and permits that allow a continued release of GHG over some pre-specified time? Should permits be issued only for the carbon-stock changes that count under the KP? With respect to national carbon taxation schemes, two questions are investigated: Should a tax credit be given for afforestation/reforestation (and a tax debit for deforestation)? Should tax credits also be given for projects that sequester carbon but do not count under the KP (such as forest protection rather than forest management)? For both schemes a crucial point is that by the formulation chosen in the KP two different classes of forest are created (i.e. those counted and those not counted under the KP), so that the implications for land prices might be significant. From a conceptual point of view this paper addresses the above-mentioned questions and contrasts some of the major

Carbon source in the future chemical industries

Science.gov (United States)

Hofmann, Peter; Heinrich Krauch, Carl

1982-11-01

Rising crude oil prices favour the exploitation of hitherto unutilised energy carriers and the realisation of new technologies in all sectors where carbon is used. These changed economic constraints necessitate both savings in conventional petrochemistry and a change to oil-independent carbon sources in the chemical industry. While, in coal chemistry, the synthesis and process principles of petrochemistry — fragmentation of the raw material and subsequent buildup of molecular structures — can be maintained, the raw material structure largely remains unchanged in the chemistry of renewable raw materials. This lecture is to demonstrate the structural as well as the technological and energy criteria of the chemistry of alternative carbon sources, to forecast the chances of commercial realization and to discuss some promising fields of research and development.

Integrated Data Fusion and Mining Techniques for Monitoring Total Organic Carbon Concentrations in a Lake

Science.gov (United States)

Total organic carbon (TOC) in surface waters, markedly of seasonal variations, is a known precursor of disinfection byproducts such as Total Trihalomethanes (TTHM) in drinking water treatment. Real-time knowledge of TOC distribution in source water can help treatment operation to...

Organic carbon dynamics in mangrove ecosystems: a review

NARCIS (Netherlands)

Kristensen, E.; Bouillon, S.; Dittmar, T.; Marchand, C.

2008-01-01

Our current knowledge on production, composition, transport, pathways and transformations of organic carbon in tropical mangrove environments is reviewed and discussed. Organic carbon entering mangrove foodwebs is either produced autochthonously or imported by tides and/or rivers. Mangrove litter

A Contemporary Assessment of Lateral Fluxes of Organic Carbon in Inland Waters of the USA and Delivery to Coastal Waters

Science.gov (United States)

Boyer, E. W.; Alexander, R. B.; Smith, R. A.; Shih, J.; Schwarz, G. E.

2010-12-01

Organic carbon (OC) is a critical water quality characteristic in surface waters, as it is an important component of the energy balance and food chains in freshwater and estuarine aquatic ecosystems, is significant in the mobilization and transport of contaminants along flow paths, and is associated with the formation of known carcinogens in drinking water supplies. The importance of OC dynamics on water quality has been recognized, but challenges remain in quantitatively addressing processes controlling OC fluxes over broad spatial scales in a hydrological context. Here, we: 1) quantified lateral OC fluxes in rivers, streams, and reservoirs across the nation; 2) partitioned how much organic carbon that is stored in lakes, rivers and streams comes from allochthonous sources (produced in the terrestrial landscape) versus autochthonous sources (produced in-stream by primary production); and 3) estimated the delivery of dissolved and total forms of organic carbon to coastal estuaries and embayments. To accomplish this, we developed national-scale models of organic carbon in U.S. surface waters using the spatially referenced regression on watersheds (SPARROW) technique. This approach uses mechanistic formulations, imposes mass balance constraints, and provides a formal parameter estimation structure to statistically estimate sources and fate of OC in terrestrial and aquatic ecosystems. We make use of a GIS based framework to describe sources of organic matter and characteristics of the landscape that affect its fate and transport, from spatial databases providing characterizations of climate, land cover, primary productivity, topography, soils, geology, and water routing. We calibrated and evaluated the model with statistical estimates of organic carbon loads that were observed at 1,125 monitoring stations across the nation. Our results illustrate spatial patterns and magnitudes OC loadings in rivers and reservoirs, highlighting hot spots and suggesting origins of the

Effects of carbon source and carbon content on electrochemical performances of Li{sub 4}Ti{sub 5}O{sub 12}/C prepared by one-step solid-state reaction

Energy Technology Data Exchange (ETDEWEB)

Hu Xuebu [College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066 (China); Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan 610041 (China); Lin Ziji [China National Quality Supervision and Inspection Center for Alcoholic Beverage Products and Processed Food, Luzhou, Sichuan 646100 (China); Yang Kerun [Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan 610041 (China); Hua, Yongjian [China Aviation Lithium Battery Co. Ltd., Luoyang, Henan 471009 (China); Deng Zhenghua, E-mail: zhdeng@cioc.ac.cn [Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan 610041 (China)

2011-05-30

Highlights: > A simple route to prepare the Li{sub 4}Ti{sub 5}O{sub 12}/C by one-step solid-state reaction. > Carbon source and carbon content are two important factors on the electrochemical performances of Li{sub 4}Ti{sub 5}O{sub 12}/C. > As-prepared Li{sub 4}Ti{sub 5}O{sub 12}/C under optimized conditions shows excellent electrochemical performances. - Abstract: Li{sub 4}Ti{sub 5}O{sub 12}/C composites were synthesized by one-step solid-state reaction method using four commonly used organic compounds or organic polymers as carbon source, i.e., polyacrylate acid (PAA), citric acid (CA), maleic acid (MA) and polyvinyl alcohol (PVA). The physical characteristics of Li{sub 4}Ti{sub 5}O{sub 12}/C composites were investigated by X-ray diffraction, electron microscopy, Raman spectroscopy, particle size distribution and thermogravimetry-derivative thermogravimetry techniques. Their electrochemical properties were characterized by cyclic voltammograms, electrochemical impedance spectra, constant current charge-discharge and rate charge-discharge. These analyses indicated that the carbon source and carbon content have a great effect on the physical and electrochemical performances of Li{sub 4}Ti{sub 5}O{sub 12}/C composites. An ideal carbon source and appropriate carbon content effectively improved the electrical contact between the Li{sub 4}Ti{sub 5}O{sub 12} particles, which enhanced the discharge capacity and rate capability of Li{sub 4}Ti{sub 5}O{sub 12}/C composites. PAA was the best carbon source for the synthesis of Li{sub 4}Ti{sub 5}O{sub 12}/C composites. When the carbon content was 3.49 wt.% (LiOH.H{sub 2}O/PAA molar ratio of 1), as-prepared Li{sub 4}Ti{sub 5}O{sub 12}/C showed the maximum discharge capacity. At 0.2 C, initial capacity of the optimized sample was 168.6 mAh g{sup -1} with capacity loss of 2.8% after 50 cycles. At 8 and 10 C, it showed discharge capacities of 143.5 and 132.7 mAh g{sup -1}, with capacity loss of 8.7 and 9.9% after 50 cycles

Can heterotrophic uptake of dissolved organic carbon and zooplankton mitigate carbon budget deficits in annually bleached corals?

Science.gov (United States)

Levas, Stephen; Grottoli, Andréa G.; Schoepf, Verena; Aschaffenburg, Matthew; Baumann, Justin; Bauer, James E.; Warner, Mark E.

2016-06-01

Annual coral bleaching events due to increasing sea surface temperatures are predicted to occur globally by the mid-century and as early as 2025 in the Caribbean, and severely impact coral reefs. We hypothesize that heterotrophic carbon (C) in the form of zooplankton and dissolved organic carbon (DOC) is a significant source of C to bleached corals. Thus, the ability to utilize multiple pools of fixed carbon and/or increase the amount of fixed carbon acquired from one or more pools of fixed carbon (defined here as heterotrophic plasticity) could underlie coral acclimatization and persistence under future ocean-warming scenarios. Here, three species of Caribbean coral— Porites divaricata, P. astreoides, and Orbicella faveolata—were experimentally bleached for 2.5 weeks in two successive years and allowed to recover in the field. Zooplankton feeding was assessed after single and repeat bleaching, while DOC fluxes and the contribution of DOC to the total C budget were determined after single bleaching, 11 months on the reef, and repeat bleaching. Zooplankton was a large C source for P. astreoides, but only following single bleaching. DOC was a source of C for single-bleached corals and accounted for 11-36 % of daily metabolic demand (CHARDOC), but represented a net loss of C in repeat-bleached corals. In repeat-bleached corals, DOC loss exacerbated the negative C budgets in all three species. Thus, the capacity for heterotrophic plasticity in corals is compromised under annual bleaching, and heterotrophic uptake of DOC and zooplankton does not mitigate C budget deficits in annually bleached corals. Overall, these findings suggest that some Caribbean corals may be more susceptible to repeat bleaching than to single bleaching due to a lack of heterotrophic plasticity, and coral persistence under increasing bleaching frequency may ultimately depend on other factors such as energy reserves and symbiont shuffling.

Partitioning of carbon sources among functional pools to investigate short-term priming effects of biochar in soil: A 13C study

International Nuclear Information System (INIS)

Kerré, Bart; Hernandez-Soriano, Maria C.; Smolders, Erik

2016-01-01

Biochar sequesters carbon (C) in soils because of its prolonged residence time, ranging from several years to millennia. In addition, biochar can promote indirect C-sequestration by increasing crop yield while, potentially, reducing C-mineralization. This laboratory study was set up to evaluate effects of biochar on C-mineralization with due attention to source appointment by using 13 C isotope signatures. An arable soil (S) (7.9 g organic C, OC kg −1 ) was amended (single dose of 10 g kg −1 soil) with dried, grinded maize stover (leaves and stalks), either natural (R) or 13 C enriched (R*), and/or biochar (B/B*) prepared from the maize stover residues (450 °C). Accordingly, seven different combinations were set up (S, SR, SB, SR*, SB*, SRB*, SR*B) to trace the source of C in CO 2 (180 days), dissolved organic-C (115 days) and OC in soil aggregate fractions (90 days). The application of biochar to soil reduced the mineralization of native soil organic C but the effect on maize stover-C mineralization was not consistent. Biochar application decreased the mineralization of the non-enriched maize stover after 90 days, this being consistent with a significant reduction of dissolved organic C concentration from 45 to 18 mg L −1 . However, no significant effect was observed for the enriched maize stover, presumably due to differences between the natural and enriched materials. The combined addition of biochar and enriched maize stover significantly increased (twofold) the presence of native soil organic C or maize derived C in the free microaggregate fraction relative to soil added only with stover. Although consistent effects among C sources and biochar materials remains elusive, our outcomes indicate that some biochar products can reduce mineralization and solubilization of other sources of C while promoting their physical protection in soil particles. - Highlights: • Biochar can reduce native soil organic carbon mineralization. • Biochar can promote storage

Identification of the sources of primary organic aerosols at urban schools: A molecular marker approach

International Nuclear Information System (INIS)

Crilley, Leigh R.; Qadir, Raeed M.; Ayoko, Godwin A.; Schnelle-Kreis, Jürgen; Abbaszade, Gülcin; Orasche, Jürgen; Zimmermann, Ralf; Morawska, Lidia

2014-01-01

Children are particularly susceptible to air pollution and schools are examples of urban microenvironments that can account for a large portion of children's exposure to airborne particles. Thus this paper aimed to determine the sources of primary airborne particles that children are exposed to at school by analyzing selected organic molecular markers at 11 urban schools in Brisbane, Australia. Positive matrix factorization analysis identified four sources at the schools: vehicle emissions, biomass burning, meat cooking and plant wax emissions accounting for 45%, 29%, 16% and 7%, of the organic carbon respectively. Biomass burning peaked in winter due to prescribed burning of bushland around Brisbane. Overall, the results indicated that both local (traffic) and regional (biomass burning) sources of primary organic aerosols influence the levels of ambient particles that children are exposed at the schools. These results have implications for potential control strategies for mitigating exposure at schools. - Highlights: • Selected organic molecular markers at 11 urban schools were analyzed. • Four sources of primary organic aerosols were identified by PMF at the schools. • Both local and regional sources were found to influence exposure at the schools. • The results have implications for mitigation of children's exposure at schools. - The identification of the most important sources of primary organic aerosols at urban schools has implications for control strategies for mitigating children's exposure at schools

Biomarker and carbon isotope constraints (δ13C, Δ14C) on sources and cycling of particulate organic matter discharged by large Siberian rivers draining permafrost areas

International Nuclear Information System (INIS)

Winterfeld, Maria

2014-08-01

Circumpolar permafrost soils store about half of the global soil organic carbon pool. These huge amounts of organic matter (OM) could accumulate due to low temperatures and water saturated soil conditions over the course of millennia. Currently most of this OM remains frozen and therefore does not take part in the active carbon cycle, making permafrost soils a globally important carbon sink. Over the last decades mean annual air temperatures in the Arctic increased stronger than the global mean and this trend is projected to continue. As a result the permafrost carbon pool is under climate pressure possibly creating a positive climate feedback due to the thaw-induced release of greenhouse gases to the atmosphere. Arctic warming will lead to increased annual permafrost thaw depths and Arctic river runoff likely resulting in enhanced mobilization and export of old, previously frozen soil-derived OM. Consequently, the great arctic rivers play an important role in global biogeochemical cycles by connecting the large permafrost carbon pool of their hinterlands with the arctic shelf seas and the Arctic Ocean. The first part of this thesis deals with particulate organic matter (POM) from the Lena Delta and adjacent Buor Khaya Bay. The Lena River in central Siberia is one of the major pathways translocating terrestrial OM from its southernmost reaches near Lake Baikal to the coastal zone of the Laptev Sea. The permafrost soils from the Lena catchment area store huge amounts of pre-aged OM, which is expected to be remobilized due to climate warming. To characterize the composition and vegetation sources of OM discharged by the Lena River, the lignin phenol and carbon isotopic composition (δ 13 C and Δ 14 C) in total suspended matter (TSM) from surface waters, surface sediments from the Buor Khaya Bay along with soils from the Lena Delta's first (Holocene) and third terraces (Pleistocene ice complex) were analyzed. The lignin compositions of these samples are

Mesoporous carbon-zirconium oxide nanocomposite derived from carbonized metal organic framework: A coating for solid-phase microextraction.

Science.gov (United States)

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%. Copyright © 2016 Elsevier B.V. All rights reserved.

Net removal of dissolved organic carbon in the anoxic waters of the Black Sea

NARCIS (Netherlands)

Margolin, A.R.; Gerringa, L.J.A.; Hansell, D.A.; Rijkenberg, M.J.A.

2016-01-01

Dissolved organic carbon (DOC) concentrations in the deep Black Sea are ~2.5 times higher than found in the globalocean. The two major external sources of DOC are rivers and the Sea of Marmara, a transit point for waters from theMediterranean Sea. In addition, expansive phytoplankton blooms

Uptake of dissolved organic carbon and trace elements by zebra mussels

Science.gov (United States)

Roditi, Hudson A.; Fisher, Nicholas S.; Sañudo-Wilhelmy, Sergio A.

2000-09-01

Zebra mussels (Dreissena polymorpha) are widespread and abundant in major freshwater ecosystems in North America, even though the phytoplankton food resources in some of these systems seem to be too low to sustain them. Because phytoplankton biomass is greatly depleted in ecosystems with large D. polymorpha populations and bacteria do not seem to be an important food source for this species, exploitation of alternative carbon sources may explain the unexpected success of D. polymorpha in such environments. Here we examine the possibility that absorption of dissolved organic carbon (DOC) from water could provide a nutritional supplement to zebra mussels. We find that mussels absorb 14C-labelled DOC produced by cultured diatoms with an efficiency of 0.23%; this indicates that DOC in natural waters could contribute up to 50% of the carbon demand of zebra mussels. We also find that zebra mussels absorb some dissolved metals that have been complexed by the DOM; although absorption of dissolved selenium was unaffected by DOC, absorption of dissolved cadmium, silver and mercury by the mussels increased 32-, 8.7- and 3.6-fold, respectively, in the presence of high-molecular-weight DOC.

[Effects of different cultivation patterns on soil aggregates and organic carbon fractions].

Science.gov (United States)

Qiu, Xiao-Lei; Zong, Liang-Gang; Liu, Yi-Fan; Du, Xia-Fei; Luo, Min; Wang, Run-Chi

2015-03-01

Combined with the research in an organic farm in the past 10 years, differences of soil aggregates composition, distribution and organic carbon fractions between organic and conventional cultivation were studied by simultaneous sampling analysis. The results showed that the percentages of aggregates (> 1 mm, 1-0.5 mm, 0.5-0.25 mm and organic cultivation were 9.73%, 18.41%, 24.46% and 43.90%, respectively. The percentage of organic cultivation than that in conventional cultivation. Organic cultivation increased soil organic carbon (average of 17.95 g x kg(-1)) and total nitrogen contents (average of 1.51 g x kg(-1)). Among the same aggregates in organic cultivation, the average content of heavy organic carbon fraction was significantly higher than that in conventional cultivation. This fraction accumulated in organic carbon. In organic cultivation, the content of labile organic carbon in > 1 mm macro-aggregates was significantly higher than that in conventional cultivation, while no significant difference was found among the other aggregates, indicating that the labile organic carbon was enriched in > 1 mm macro-aggregates. Organic cultivation increased the amounts of organic carbon and its fractions, reduced tillage damage to aggregates, and enhanced the stability of organic carbon. Organic cultivation was therefore beneficial for soil carbon sequestration. The findings of this research may provide theoretical basis for further acceleration of the organic agriculture development.

Satellite observation of particulate organic carbon dynamics in ...

Science.gov (United States)

Particulate organic carbon (POC) plays an important role in coastal carbon cycling and the formation of hypoxia. Yet, coastal POC dynamics are often poorly understood due to a lack of long-term POC observations and the complexity of coastal hydrodynamic and biogeochemical processes that influence POC sources and sinks. Using field observations and satellite ocean color products, we developed a nw multiple regression algorithm to estimate POC on the Louisiana Continental Shelf (LCS) from satellite observations. The algorithm had reliable performance with mean relative error (MRE) of ?40% and root mean square error (RMSE) of ?50% for MODIS and SeaWiFS images for POC ranging between ?80 and ?1200 mg m23, and showed similar performance for a large estuary (Mobile Bay). Substantial spatiotemporal variability in the satellite-derived POC was observed on the LCS, with high POC found on the inner shelf (satellite data with carefully developed algorithms can greatly increase

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

Science.gov (United States)

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.

Immobilized Tannin from Sanseviera trifasciata on Carbon as Adsorbent For Iron(II in Polluted Water Source

Directory of Open Access Journals (Sweden)

Irfan Hanafi Arif

2016-03-01

Full Text Available The organic-agricultural waste resulted from local farmer or community gardening recently paid public attention. The presence and easily grown of “Lidah Mertua” or Sanseviera trifasciata being focused on potency investigation for its prospecting application. It was reported contain some phenolic and also tannin extracted from aqueous solvents. This paper revealed recent investigation applying of its isolated tannin from leave part to modifying of activated carbon. The previous report published that carbon were able to adsorb some toxic heavy metals. However, it has some limitation including lower capacity adsorption. Impregnated or immobilized the tannin-isolated from S. trifasciata leaves was able to modify the carbon functionality, physical appearance, pores size, and it adsorption capacity. Both Langmuir and Freundlich adsorption mechanism model also disclosed the developed adsorbent mechanism of iron(II adsorption on the adsorbent tannin-immobolized on carbon. The real test using community well drilling water source also gave important finding on the concentration of iron(II contained on water source.

Insights in groundwater organic matter from Liquid Chromatography-Organic Carbon Detection

Science.gov (United States)

Rutlidge, H.; Oudone, P.; McDonough, L.; Andersen, M. S.; Baker, A.; Meredith, K.; O'Carroll, D. M.

2017-12-01

Understanding the processes that control the concentration and characteristics of organic matter in groundwater has important implications for the terrestrial global carbon budget. Liquid Chromatography - Organic Carbon Detection (LC-OCD) is a size-exclusion based chromatography technique that separates the organic carbon into molecular weight size fractions of biopolymers, humic substances, building blocks (degradation products of humic substances), low molecular weight acids and low molecular weight neutrals. Groundwater and surface water samples were collected from a range of locations in Australia representing different surface soil, land cover, recharge type and hydrological properties. At one site hyporheic zone samples were also collected from beneath a stream. The results showed a general decrease in the aromaticity and molecular weight indices going from surface water, hyporheic downwelling and groundwater samples. The aquifer substrate also affected the organic composition. For example, groundwater samples collected from a zone of fractured rock showed a relative decrease in the proportion of humic substances, suggestive of sorption or degradation of humic substances. This work demonstrates the potential for using LC-OCD in elucidating the processes that control the concentration and characteristics of organic matter in groundwater.

Mapping soil organic carbon content and composition across Australia to assess vulnerability to climate change

Science.gov (United States)

Viscarra Rossel, R. A.

2015-12-01

We can effectively monitor soil condition—and develop sound policies to offset the emissions of greenhouse gases—only with accurate data from which to define baselines. Currently, estimates of soil organic C for countries or continents are either unavailable or largely uncertain because they are derived from sparse data, with large gaps over many areas of the Earth. Here, we derive spatially explicit estimates, and their uncertainty, of the distribution and stock of organic C content and composition in the soil of Australia. The composition of soil organic C may be characterized by chemical separation or physical fractionation based on either particle size or particle density (Skjemstad et al., 2004; Gregorich et al., 2006; Kelleher&Simpson, 2006; Zimmermann et al., 2007). In Australia, for example, Skjemstad et al. (2004) used physical separation of soil samples into 50-2000 and solid-state 13C nuclear magnetic resonance (NMR) spectroscopy, giving the three OC pools, particulate organic carbon (POC), humic organic carbon (HOC) and resistant organic carbon (ROC; charcoal or char-carbon). We assembled and harmonized data from several sources to produce the most comprehensive set of data on the current stock of organic C in soil of the continent. Using them, we have produced a fine spatial resolution baseline map of organic C, POC, HOC and ROC at the continental scale. In this presentation I will describe how we made the maps and how we use them to assess the vulnerability of soil organic C to for instance climate change.

Cassava stillage and its anaerobic fermentation liquid as external carbon sources in biological nutrient removal.

Science.gov (United States)

Bu, Fan; Hu, Xiang; Xie, Li; Zhou, Qi

2015-04-01

The aim of this study was to investigate the effects of one kind of food industry effluent, cassava stillage and its anaerobic fermentation liquid, on biological nutrient removal (BNR) from municipal wastewater in anaerobic-anoxic-aerobic sequencing batch reactors (SBRs). Experiments were carried out with cassava stillage supernatant and its anaerobic fermentation liquid, and one pure compound (sodium acetate) served as an external carbon source. Cyclic studies indicated that the cassava by-products not only affected the transformation of nitrogen, phosphorus, poly-β-hydroxyalkanoates (PHAs), and glycogen in the BNR process, but also resulted in higher removal efficiencies for phosphorus and nitrogen compared with sodium acetate. Furthermore, assays for phosphorus accumulating organisms (PAOs) and denitrifying phosphorus accumulating organisms (DPAOs) demonstrated that the proportion of DPAOs to PAOs reached 62.6% (Day 86) and 61.8% (Day 65) when using cassava stillage and its anaerobic fermentation liquid, respectively, as the external carbon source. In addition, the nitrate utilization rates (NURs) of the cassava by-products were in the range of 5.49-5.99 g N/(kg MLVSS⋅h) (MLVSS is mixed liquor volatile suspended solids) and 6.63-6.81 g N/(kg MLVSS⋅h), respectively. The improvement in BNR performance and the reduction in the amount of cassava stillage to be treated in-situ make cassava stillage and its anaerobic fermentation liquid attractive alternatives to sodium acetate as external carbon sources for BNR processes.

Cassava stillage and its anaerobic fermentation liquid as external carbon sources in biological nutrient removal*

Science.gov (United States)

Bu, Fan; Hu, Xiang; Xie, Li; Zhou, Qi

2015-01-01

The aim of this study was to investigate the effects of one kind of food industry effluent, cassava stillage and its anaerobic fermentation liquid, on biological nutrient removal (BNR) from municipal wastewater in anaerobic-anoxic-aerobic sequencing batch reactors (SBRs). Experiments were carried out with cassava stillage supernatant and its anaerobic fermentation liquid, and one pure compound (sodium acetate) served as an external carbon source. Cyclic studies indicated that the cassava by-products not only affected the transformation of nitrogen, phosphorus, poly-β-hydroxyalkanoates (PHAs), and glycogen in the BNR process, but also resulted in higher removal efficiencies for phosphorus and nitrogen compared with sodium acetate. Furthermore, assays for phosphorus accumulating organisms (PAOs) and denitrifying phosphorus accumulating organisms (DPAOs) demonstrated that the proportion of DPAOs to PAOs reached 62.6% (Day 86) and 61.8% (Day 65) when using cassava stillage and its anaerobic fermentation liquid, respectively, as the external carbon source. In addition, the nitrate utilization rates (NURs) of the cassava by-products were in the range of 5.49–5.99 g N/(kg MLVSS∙h) (MLVSS is mixed liquor volatile suspended solids) and 6.63–6.81 g N/(kg MLVSS∙h), respectively. The improvement in BNR performance and the reduction in the amount of cassava stillage to be treated in-situ make cassava stillage and its anaerobic fermentation liquid attractive alternatives to sodium acetate as external carbon sources for BNR processes. PMID:25845364

Carbon and Nitrogen Sources for Shrimp Postlarvae Fed Natural Diets from a Tropical Mangrove System

Science.gov (United States)

Dittel, A. I.; Epifanio, C. E.; Cifuentes, L. A.; Kirchman, D. L.

1997-11-01

Postlarvae ofPenaeus vannameiwere fed various diets in order to examine the importance of detritus and other possible prey items in supporting postlarval growth. Stable isotopes (C and N) were used to determine the carbon and nitrogen source of the prey in the various diets. The zooplankton diet contained mostly copepods. The subtidal detritus treatment consisted mostly of plant material whereas the diets from both intertidal sites contained a mixture of plant detritus and associated meiofauna. Postlarvae reared on zooplankton and detritus plus meiofauna diets more than tripled their weight during a 6-day period. In contrast, postlarvae fed the detritus diet barely doubled their weight. Based on isotopic composition, postlarvae appear to obtain their carbon and nitrogen from various food sources. Postlarvae were enriched by 0·4‰ in13C and 2·7‰ in15N relative to the zooplankton diet, which is consistent with isotopic fractionation between successive trophic levels. In turn, the isotopic signal of the zooplankton was consistent with phytoplankton being the initial source of organic matter. In contrast, mean δ13C values of the shrimp fed detritus plus meiofauna were significantly different from their respective diets. Isotopic ratios of the postlarvae fed the mixed diet from Chomes were two trophic levels above benthic algae suggesting that the shrimp preyed on organisms that derived their carbon and nitrogen from benthic algae and/or phytoplankton.

Potential for long-term transfer of dissolved organic carbon from riparian zones to streams in boreal catchments.

Science.gov (United States)

Ledesma, José L J; Grabs, Thomas; Bishop, Kevin H; Schiff, Sherry L; Köhler, Stephan J

2015-08-01

Boreal regions store most of the global terrestrial carbon, which can be transferred as dissolved organic carbon (DOC) to inland waters with implications for both aquatic ecology and carbon budgets. Headwater riparian zones (RZ) are important sources of DOC, and often just a narrow 'dominant source layer' (DSL) within the riparian profile is responsible for most of the DOC export. Two important questions arise: how long boreal RZ could sustain lateral DOC fluxes as the sole source of exported carbon and how its hydromorphological variability influences this role. We estimate theoretical turnover times by comparing carbon pools and lateral exports in the DSL of 13 riparian profiles distributed over a 69 km(2) catchment in northern Sweden. The thickness of the DSL was 36 ± 18 (average ± SD) cm. Thus, only about one-third of the 1-m-deep riparian profile contributed 90% of the lateral DOC flux. The 13 RZ exported 8.7 ± 6.5 g C m(-2) year(-1) , covering the whole range of boreal stream DOC exports. The variation could be explained by local hydromorphological characteristics including RZ width (R(2) = 0.90). The estimated theoretical turnover times were hundreds to a few thousands of years, that is there is a potential long-lasting supply of DOC. Estimates of net ecosystem production in the RZ suggest that lateral fluxes, including both organic and inorganic C, could be maintained without drawing down the riparian pools. This was supported by measurements of stream DO(14) C that indicated modern carbon as the predominant fraction exported, including streams disturbed by ditching. The transfer of DOC into boreal inland waters from new and old carbon sources has a major influence on surface water quality and global carbon balances. This study highlights the importance of local variations in RZ hydromorphology and DSL extent for future DOC fluxes under a changing climate. © 2015 The Authors. Global Change Biology Published by John Wiley & Sons Ltd.

Evaluating Late Cretaceous OAEs and the influence of marine incursions on organic carbon burial in an expansive East Asian paleo-lake

Science.gov (United States)

Jones, Matthew M.; Ibarra, Daniel E.; Gao, Yuan; Sageman, Bradley B.; Selby, David; Chamberlain, C. Page; Graham, Stephan A.

2018-02-01

Expansive Late Cretaceous lacustrine deposits of East Asia offer unique stratigraphic records to better understand regional responses to global climate events, such as oceanic anoxic events (OAEs), and terrestrial organic carbon burial dynamics. This study presents bulk organic carbon isotopes (δ13Corg), elemental concentrations (XRF), and initial osmium ratios (187Os/188Os, Osi) from the Turonian-Coniacian Qingshankou Formation, a ∼5 Ma lacustrine mudstone succession in the Songliao Basin of northeast China. A notable δ13Corg excursion (∼ + 2.5‰) in organic carbon-lean Qingshankou Members 2-3 correlates to OAE3 in the Western Interior Basin (WIB) of North America within temporal uncertainty of high-precision age models. Decreases in carbon isotopic fractionation (Δ13C) through OAE3 in the WIB and Songliao Basin, suggest that significantly elevated global rates of organic carbon burial drew down pCO2, likely cooling climate. Despite this, Osi chemostratigraphy demonstrates no major changes in global volcanism or weathering trends through OAE3. Identification of OAE3 in a lake system is consistent with lacustrine records of other OAEs (e.g., Toarcian OAE), and underscores that terrestrial environments were sensitive to climate perturbations associated with OAEs. Additionally, the relatively radiogenic Osi chemostratigraphy and XRF data confirm that the Qingshankou Formation was deposited in a non-marine setting. Organic carbon-rich intervals preserve no compelling Osi evidence for marine incursions, an existing hypothesis for generating Member 1's prolific petroleum source rocks. Based on our results, we present a model for water column stratification and source rock deposition independent of marine incursions, detailing dominant biogeochemical cycles and lacustrine organic carbon burial mechanisms.

Organic carbon in Hanford single-shell tank waste

International Nuclear Information System (INIS)

Toth, J.J.; Willingham, C.E.; Heasler, P.G.; Whitney, P.D.

1994-04-01

Safety of Hanford single-shell tanks (SSTs) containing organic carbon is a concern because the carbon in the presence of oxidizers (NO 3 or NO 2 ) is combustible when sufficiently concentrated and exposed to elevated temperatures. A propagating chemical reaction could potentially occur at high temperature (above 200 C). The rapid increase in temperature and pressure within a tank might result in the release of radioactive waste constituents to the environment. The purpose of this study is to gather available laboratory information about the organic carbon waste inventories stored in the Hanford SSTs. Specifically, the major objectives of this investigation are: Review laboratory analytical data and measurements for SST composite core and supernatant samples for available organic data; Assess the correlation of organic carbon estimated utilizing the TRAC computer code compared to laboratory measurements; and From the laboratory analytical data, estimate the TOC content with confidence levels for each of the 149 SSTs

Fertilization increases paddy soil organic carbon density*

Science.gov (United States)

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

Fertilization increases paddy soil organic carbon density.

Science.gov (United States)

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

2012-04-01

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.

Characterization and source apportionment of atmospheric organic and elemental carbon during fall and winter of 2003 in Xi'an, China

Directory of Open Access Journals (Sweden)

J. J. Cao

2005-01-01

Full Text Available Continuous measurements of atmospheric organic and elemental carbon (OC and EC were taken during the high-pollution fall and winter seasons at Xi'an, Shaanxi Province, China from September 2003 through February 2004. Battery-powered mini-volume samplers collected PM2.5 samples daily and PM10 samples every third day. Samples were also obtained from the plumes of residential coal combustion, motor-vehicle exhaust, and biomass burning sources. These samples were analyzed for OC/EC by thermal/optical reflectance (TOR following the Interagency Monitoring of Protected Visual Environments (IMPROVE protocol. OC and EC levels at Xi'an are higher than most urban cities in Asia. Average PM2.5 OC concentrations in fall and winter were 34.1±18.0 μg m−3 and 61.9±;33.2 μg m−3, respectively; while EC concentrations were 11.3±6.9 μg m−3 and 12.3±5.3 μg m−3, respectively. Most of the OC and EC were in the PM2.5 fraction. OC was strongly correlated (R>0.95 with EC in the autumn and moderately correlated (R=0.81 with EC during winter. Carbonaceous aerosol (OC×1.6+EC accounted for 48.8%±10.1% of the PM2.5 mass during fall and 45.9±7.5% during winter. The average OC/EC ratio was 3.3 in fall and 5.1 in winter, with individual OC/EC ratios nearly always exceeding 2.0. The higher wintertime OC/EC corresponded to increased residential coal combustion for heating. Total carbon (TC was associated with source contributions using absolute principal component analysis (APCA with eight thermally-derived carbon fractions. During fall, 73% of TC was attributed to gasoline engine exhaust, 23% to diesel exhaust, and 4% to biomass burning. During winter, 44% of TC was attributed to gasoline engine exhaust, 44% to coal burning, 9% to biomass burning, and 3% to diesel engine exhaust.

The carbon commute: Effects of urbanization on dissolved organic carbon quality on a suburban New England river network

Science.gov (United States)

Balch, E.; Robison, A.; Wollheim, W. M.

2017-12-01

Understanding anthropogenic influence on the sources and fluxes of carbon is necessary for interpreting the carbon cycle and contaminant transport throughout a river system. As urbanization increases worldwide, it is critical to understand how urbanization affects the carbon cycle so that we may be able to predict future changes. Rivers act as both transporters of terrestrial dissolved organic carbon (DOC) to coastal regions, and active transformers of DOC. The character (lability) of the carbon found within a river network is influenced by its sources and fluxes, as determined by the ecological processes, land use, and discharge, which vary throughout the network. We have characterized DOC quantity and quality throughout a suburban New England river network (Ipswich River, MA) in an attempt to provide a detailed picture of how DOC quality varies within a network, and how urbanization influences these changes. We conducted a synoptic survey of 45 sites over two hydrologically similar days in the Ipswich River network in northeast Massachusetts, USA. We collected discrete grab samples for DOC quantity and quality analyses. We also collected dissolved oxygen, conductivity, and nutrients (major anions and cations) as an extension of the synoptic survey. We plan to determine the source of the DOC by using excitation-emission matrices (EEMs), and specific UV absorption (SUVA) at 254 nm. These analyses will provide us with a detailed picture of how DOC quality varies within a network, and how urbanization influences these changes. Using land use data of the Ipswich River watershed, we are able to model the changes in DOC quality throughout the network. In highly urbanized headwaters, through the progressively more forested and wetland dominated main stem reaches, we expect to see the imprint of urbanization throughout the network due to its decreased lability. Studying the imprint of urbanization on DOC throughout a river network helps us complete our understanding of

Effects of added fertilizers and carbon source on the persistence of carbaryl in soils

International Nuclear Information System (INIS)

Hirata, R.; Lord, K.A.; Luchini, L.C.; Mesquita, T.B.; Ruegg, E.F.

1980-01-01

The effect of added fertilizers and carbon source on the persistence of carbaryl in two types of soils was investigated using the technique of liquid scintillation counting. In both soils, the addition of fertilzers (NPK) had little effect on the rate of degradation of carbaryl. In contrast, the addition of sucrose, with or without fertilizer increases degradation of carboryl in a yellow red latosol soil poor in organic matter but has little effect on the degradation in a humic gley soil rich in organic mutter. (Author) [pt

Water extraction of coals - potential for estimating low molecular weight organic acids as carbon feedstock for the deep terrestrial biosphere

Energy Technology Data Exchange (ETDEWEB)

Vieth, A.; Mangelsdorf, K.; Sykes, R.; Horsfield, B. [Geoforschungszentrum Potsdam, Potsdam (Germany)

2008-08-15

With the recent increasing interest in the deep biosphere, the question arises as to where the carbon sources that support deep microbial communities are derived from. Our research was focussed on the water-soluble, low molecular weight (LMW) organic acids that are potentially available from different sedimentary lithologies to serve as a carbon source to feed the deep biosphere. A series of Eocene-Pleistocene coals, mudstones and sandstones of varying rank (maturity) and total organic carbon (TOC) content from the Waikato Basin, New Zealand, has been Soxhlet-extracted using water. The combined concentration of recovered formate, acetate and oxalate range from 366 to 2499 {mu} g/g sediment and appear to be dependent on rank, organofacies and TOC. The yields indicate the potential of carbonaceous sediments to feed the local deep terrestrial biosphere over geological periods of time. The existence of living microbial organisms in the mudstones and sandstones was proved by the identification of intact phospholipids (PLs).

Metabolic engineering of Corynebacterium glutamicum aimed at alternative carbon sources and new products

Directory of Open Access Journals (Sweden)

Volker Fritz Wendisch

2012-10-01

Full Text Available Corynebacterium glutamicum is well known as the amino acid-producing workhorse of fermentation industry, being used for multi-million-ton scale production of glutamate and lysine for more than 60 years. However, it is only recently that extensive research has focused on engineering it beyond the scope of amino acids. Meanwhile, a variety of corynebacterial strains allows access to alternative carbon sources and/or allows production of a wide range of industrially relevant compounds. Some of these efforts set new standards in terms of titers and productivities achieved whereas others represent a proof-of-principle. These achievements manifest the position of C. glutamicum as an important industrial microorganism with capabilities far beyond the traditional amino acid production. In this review we focus on the state of the art of metabolic engineering of C. glutamicum for utilization of alternative carbon sources, (e.g. coming from wastes and unprocessed sources, and construction of C. glutamicum strains for production of new products such as diamines, organic acids and alcohols.

Biomass Burning Emissions of Black Carbon from African Sources

Science.gov (United States)

Aiken, A. C.; Leone, O.; Nitschke, K. L.; Dubey, M. K.; Carrico, C.; Springston, S. R.; Sedlacek, A. J., III; Watson, T. B.; Kuang, C.; Uin, J.; McMeeking, G. R.; DeMott, P. J.; Kreidenweis, S. M.; Robinson, A. L.; Yokelson, R. J.; Zuidema, P.

2016-12-01

Biomass burning (BB) emissions are a large source of carbon to the atmosphere via particles and gas phase species. Carbonaceous aerosols are emitted along with gas-phase carbon monoxide (CO) and carbon dioxide (CO2) that can be used to determine particulate emission ratios and modified combustion efficiencies. Black carbon (BC) aerosols are potentially underestimated in global models and are considered to be one of the most important global warming factors behind CO2. Half or more BC in the atmosphere is from BB, estimated at 6-9 Tg/yr (IPCC, 5AR) and contributing up to 0.6 W/m2 atmospheric warming (Bond et al., 2013). With a potential rise in drought and extreme events in the future due to climate change, these numbers are expected to increase. For this reason, we focus on BC and organic carbon aerosol species that are emitted from forest fires and compare their emission ratios, physical and optical properties to those from controlled laboratory studies of single-source BB fuels to understand BB carbonaceous aerosols in the atmosphere. We investigate BC in concentrated BB plumes as sampled from the new U.S. DOE ARM Program campaign, Layered Atlantic Smoke Interactions with Clouds (LASIC). The ARM Aerosol Mobile Facility 1 (AMF1) and Mobile Aerosol Observing System (MAOS) are currently located on Ascension Island in the South Atlantic Ocean, located midway between Angola and Brazil. The location was chosen for sampling maximum aerosol outflow from Africa. The far-field aged BC from LASIC is compared to BC from indoor generation from single-source fuels, e.g. African grass, sampled during Fire Lab At Missoula Experiments IV (FLAME-IV). BC is measured with a single-particle soot photometer (SP2) alongside numerous supporting instrumentation, e.g. particle counters, CO and CO2 detectors, aerosol scattering and absorption measurements, etc. FLAME-IV includes both direct emissions and well-mixed aerosol samples that have undergone dilution, cooling, and condensation. BC

The effect of microbial activity and adsorption processes on groundwater dissolved organic carbon character and concentration

Science.gov (United States)

Meredith, K.; McDonough, L.; Oudone, P.; Rutlidge, H.; O'Carroll, D. M.; Andersen, M. S.; Baker, A.

2017-12-01

Balancing the terrestrial global carbon budget has proven to be a significant challenge. Whilst the movement of carbon in the atmosphere, rivers and oceans has been extensively studied, the potential for groundwater to act as a carbon source or sink through both microbial activity and sorption to and from mineral surfaces, is poorly understood. To investigate the biodegradable component of groundwater dissolved organic carbon (DOC), groundwater samples were collected from multiple coastal and inland sites. Water quality parameters such as pH, electrical conductivity, temperature, dissolved oxygen were measured in the field. Samples were analysed and characterised for their biodegradable DOC content using spectrofluorometric and Liquid Chromatography-Organic Carbon Detection (LC-OCD) techniques at set intervals within a 28 day period. Further to this, we performed laboratory sorption experiments on our groundwater samples using different minerals to examine the effect of adsorption processes on DOC character and concentration. Calcium carbonate, quartz and iron coated quartz were heated to 400ºC to remove potential carbon contamination, and then added at various known masses (0 mg to 10 g) to 50 mL of groundwater. Samples were then rotated for two hours, filtered at 0.2 μm and analysed by LC-OCD. This research forms part of an ongoing project which will assist in identifying the factors affecting the mobilisation, transport and removal of DOC in uncontaminated groundwater. By quantifying the relative importance of these processes, we can then determine whether the groundwater is a carbon source or sink. Importantly, this information will help guide policy and identify the need to include groundwater resources as part of the carbon economy.

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

Science.gov (United States)

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

Partitioning of carbon sources among functional pools to investigate short-term priming effects of biochar in soil: A {sup 13}C study

Energy Technology Data Exchange (ETDEWEB)

Kerré, Bart [Department of Earth and Environmental Science, KU Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee (Belgium); Hernandez-Soriano, Maria C., E-mail: m.hernandezsoriano@uq.edu.au [Department of Earth and Environmental Science, KU Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee (Belgium); The University of Queensland, School of Agriculture and Food Sciences, St. Lucia, Queensland 4072 (Australia); Smolders, Erik [Department of Earth and Environmental Science, KU Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee (Belgium)

2016-03-15

Biochar sequesters carbon (C) in soils because of its prolonged residence time, ranging from several years to millennia. In addition, biochar can promote indirect C-sequestration by increasing crop yield while, potentially, reducing C-mineralization. This laboratory study was set up to evaluate effects of biochar on C-mineralization with due attention to source appointment by using {sup 13}C isotope signatures. An arable soil (S) (7.9 g organic C, OC kg{sup −1}) was amended (single dose of 10 g kg{sup −1} soil) with dried, grinded maize stover (leaves and stalks), either natural (R) or {sup 13}C enriched (R*), and/or biochar (B/B*) prepared from the maize stover residues (450 °C). Accordingly, seven different combinations were set up (S, SR, SB, SR*, SB*, SRB*, SR*B) to trace the source of C in CO{sub 2} (180 days), dissolved organic-C (115 days) and OC in soil aggregate fractions (90 days). The application of biochar to soil reduced the mineralization of native soil organic C but the effect on maize stover-C mineralization was not consistent. Biochar application decreased the mineralization of the non-enriched maize stover after 90 days, this being consistent with a significant reduction of dissolved organic C concentration from 45 to 18 mg L{sup −1}. However, no significant effect was observed for the enriched maize stover, presumably due to differences between the natural and enriched materials. The combined addition of biochar and enriched maize stover significantly increased (twofold) the presence of native soil organic C or maize derived C in the free microaggregate fraction relative to soil added only with stover. Although consistent effects among C sources and biochar materials remains elusive, our outcomes indicate that some biochar products can reduce mineralization and solubilization of other sources of C while promoting their physical protection in soil particles. - Highlights: • Biochar can reduce native soil organic carbon mineralization. �

PM2.5 source apportionment with organic markers in the Southeastern Aerosol Research and Characterization (SEARCH) study.

Science.gov (United States)

Watson, John G; Chow, Judith C; Lowenthal, Douglas H; Antony Chen, L-W; Shaw, Stephanie; Edgerton, Eric S; Blanchard, Charles L

2015-09-01

Positive matrix factorization (PMF) and effective variance (EV) solutions to the chemical mass balance (CMB) were applied to PM(2.5) (particulate matter with an aerodynamic diameter thermal carbon fraction concentrations were supplemented with detailed nonpolar organic speciation by thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS). Source contribution estimates were calculated for motor vehicle exhaust, biomass burning, cooking, coal-fired power plants, road dust, vegetative detritus, and secondary sulfates and nitrates for Atlanta. Similar sources were found for Birmingham, with the addition of an industrial source and the separation of biomass burning into open burning and residential wood combustion. EV-CMB results based on conventional species were qualitatively similar to those estimated by PMF-CMB. Secondary ammonium sulfate was the largest contributor, accounting for 27-38% of PM(2.5), followed by biomass burning (21-24%) and motor vehicle exhaust (9-24%) at both sites, with 4-6% of PM(2.5) attributed to coal-fired power plants by EV-CMB. Including organic compounds in the EV-CMB reduced the motor vehicle exhaust and biomass burning contributions at both sites, with a 13-23% deficit for PM(2.5) mass. The PMF-CMB solution showed mixing of sources within the derived factors, both with and without the addition of speciated organics, as is often the case with complex source mixtures such as those at these urban-scale sites. The nonpolar TD-GC/MS compounds can be obtained from existing filter samples and are a useful complement to the elements, ions, and carbon fractions. However, they should be supplemented with other methods, such as TD-GC/MS on derivitized samples, to obtain a wider range of polar compounds such as sterols, sugars, and organic acids. The PMF and EV solutions to the CMB equations are complementary to, rather than replacements for, each other, as comparisons of their results reveal uncertainties that are not otherwise evident

Influence of Carbon Sources and Electron Shuttles on Ferric Iron Reduction by Cellulomonas sp. Strain ES6

Energy Technology Data Exchange (ETDEWEB)

Dr Robin Gerlach; Erin K. Field; Sridhar Viamajala; Brent M. Peyton; William A. Apel; Al B. Cunningham

2011-09-01

Microbially reduced iron minerals can reductively transform a variety of contaminants including heavy metals, radionuclides, chlorinated aliphatics, and nitroaromatics. A number of Cellulomonas spp. strains, including strain ES6, isolated from aquifer samples obtained at the U.S. Department of Energy's Hanford site in Washington, have been shown to be capable of reducing Cr(VI), TNT, natural organic matter, and soluble ferric iron [Fe(III)]. This research investigated the ability of Cellulomonas sp. strain ES6 to reduce solid phase and dissolved Fe(III) utilizing different carbon sources and various electron shuttling compounds. Results suggest that Fe(III) reduction by and growth of strain ES6 was dependent upon the type of electron donor, the form of iron present, and the presence of synthetic or natural organic matter, such as anthraquinone-2,6-disulfonate (AQDS) or humic substances. This research suggests that Cellulomonas sp. strain ES6 could play a significant role in metal reduction in the Hanford subsurface and that the choice of carbon source and organic matter addition can allow for independent control of growth and iron reduction activity.

Watershed scale spatial variability in dissolved and total organic and inorganic carbon in contrasting UK catchments

Science.gov (United States)

Cumberland, S.; Baker, A.; Hudson, N. J.

2006-12-01

Approximately 800 organic and inorganic carbon analyses have been undertaken from watershed scale and regional scale spatial surveys in various British catchments. These include (1) a small (urban catchment (Ouseburn, N England); (2) a headwater, lowland agricultural catchment (River Tern, C England) (3) a large UK catchment (River Tyne, ~3000 sq-km) and (4) a spatial survey of ~300 analyses from rivers from SW England (~1700 sq-km). Results demonstrate that: (1) the majority of organic and inorganic carbon is in the dissolved (DOC and DIC) fractions; (2) that with the exception of peat rich headwaters, DIC concentration is always greater than DOC; (3) In the rural River Tern, riverine DOC and DIC are shown to follow a simple end- member mixing between DIC (DOC) rich (poor) ground waters and DOC (DIC) rich (poor) riparian wetlands for all sample sites. (4) In the urbanized Ouseburn catchment, although many sample sites also show this same mixing trend, some tributaries follow a pollutant trend of simultaneous increases in both DOC and DIC. The Ouseburn is part of the larger Tyne catchment: this larger catchment follows the simple groundwater DIC- soil water DOC end member mixing model, with the exception of the urban catchments which exhibit an elevated DIC compared to rural sites. (5) Urbanization is demonstrated to increase DIC compared to equivalent rural catchments; this DIC has potential sources including diffuse source inputs from the dissolution of concrete, point sources such as trade effluents and landfill leachates, and bedrock derived carbonates relocated to the soil dissolution zone by urban development. (6) DIC in rural SW England demonstrates that spatial variability in DIC can be attributed to variations in geology; but that DIC concentrations in the SW England rivers dataset are typically lower than the urbanized Tyne catchments despite the presence of carbonate bedrock in many of the sample catchments in the SW England dataset. (7) Recent

Long-term dynamics of dissolved organic carbon: implications for drinking water supply.

Science.gov (United States)

Ledesma, José L J; Köhler, Stephan J; Futter, Martyn N

2012-08-15

Surface waters are the main source of drinking water in many regions. Increasing organic carbon concentrations are a cause for concern in Nordic countries since both dissolved and particulate organic carbon can transport contaminants and adversely affect drinking water treatment processes. We present a long-term study of dynamics of total (particulate and dissolved) organic carbon (TOC) concentrations in the River Fyris. This river supplies drinking water to approximately 200000 people in Uppsala, Sweden. The River Fyris is a main tributary to Lake Mälaren, which supplies drinking water to approximately 2 million people in the greater Stockholm area. Utilities responsible for drinking water supply in both Uppsala and Stockholm have expressed concerns about possible increases in TOC. We evaluate organic carbon dynamics within the Fyris catchment by calculating areal mass exports using observed TOC concentrations and modeled flows and by modeling dissolved organic carbon (as a proxy for TOC) using the dynamic, process based INCA-C model. Exports of TOC from the catchment ranged from 0.8 to 5.8 g m(-2) year(-1) in the period 1995-2010. The variation in annual exports was related to climatic variability which influenced seasonality and amount of runoff. Exports and discharge uncoupled at the end of 2008. A dramatic increase in TOC concentrations was observed in 2009, which gradually declined in 2010-2011. INCA-C successfully reproduced the intra- and inter-annual variation in concentrations during 1996-2008 and 2010-2011 but failed to capture the anomalous increase in 2009. We evaluated a number of hypotheses to explain the anomaly in 2009 TOC values, ultimately none proved satisfactory. We draw two main conclusions: there is at least one unknown or unmeasured process controlling or influencing surface water TOC and INCA-C can be used as part of the decision-making process for current and future use of rivers for drinking water supply. Copyright © 2012 Elsevier B

Anthropogenic Forcing of Carbonate and Organic Carbon Preservation in Marine Sediments.

Science.gov (United States)

Keil, Richard

2017-01-03

Carbon preservation in marine sediments, supplemented by that in large lakes, is the primary mechanism that moves carbon from the active surficial carbon cycle to the slower geologic carbon cycle. Preservation rates are low relative to the rates at which carbon moves between surface pools, which has led to the preservation term largely being ignored when evaluating anthropogenic forcing of the global carbon cycle. However, a variety of anthropogenic drivers-including ocean warming, deoxygenation, and acidification, as well as human-induced changes in sediment delivery to the ocean and mixing and irrigation of continental margin sediments-all work to decrease the already small carbon preservation term. These drivers affect the cycling of both carbonate and organic carbon in the ocean. The overall effect of anthropogenic forcing in the modern ocean is to decrease delivery of carbon to sediments, increase sedimentary dissolution and remineralization, and subsequently decrease overall carbon preservation.

Constraints on primary and secondary particulate carbon sources using chemical tracer and 14C methods during CalNex-Bakersfield

Data.gov (United States)

U.S. Environmental Protection Agency — The present study investigates primary and secondary sources of organic carbon for Bakersfield, CA, USA as part of the 2010 CalNex study. The method used here...

Carbon Storages in Plantation Ecosystems in Sand Source Areas of North Beijing, China

Science.gov (United States)

Liu, Xiuping; Zhang, Wanjun; Cao, Jiansheng; Shen, Huitao; Zeng, Xinhua; Yu, Zhiqiang; Zhao, Xin

2013-01-01

Afforestation is a mitigation option to reduce the increased atmospheric carbon dioxide levels as well as the predicted high possibility of climate change. In this paper, vegetation survey data, statistical database, National Forest Resource Inventory database, and allometric equations were used to estimate carbon density (carbon mass per hectare) and carbon storage, and identify the size and spatial distribution of forest carbon sinks in plantation ecosystems in sand source areas of north Beijing, China. From 2001 to the end of 2010, the forest areas increased more than 2.3 million ha, and total carbon storage in forest ecosystems was 173.02 Tg C, of which 82.80 percent was contained in soil in the top 0–100 cm layer. Younger forests have a large potential for enhancing carbon sequestration in terrestrial ecosystems than older ones. Regarding future afforestation efforts, it will be more effective to increase forest area and vegetation carbon density through selection of appropriate tree species and stand structure according to local climate and soil conditions, and application of proper forest management including land-shaping, artificial tending and fencing plantations. It would be also important to protect the organic carbon in surface soils during forest management. PMID:24349223

[Roles of soil dissolved organic carbon in carbon cycling of terrestrial ecosystems: a review].

Science.gov (United States)

Li, Ling; Qiu, Shao-Jun; Liu, Jing-Tao; Liu, Qing; Lu, Zhao-Hua

2012-05-01

Soil dissolved organic carbon (DOC) is an active fraction of soil organic carbon pool, playing an important role in the carbon cycling of terrestrial ecosystems. In view of the importance of the carbon cycling, this paper summarized the roles of soil DOC in the soil carbon sequestration and greenhouse gases emission, and in considering of our present ecological and environmental problems such as soil acidification and climate warming, discussed the effects of soil properties, environmental factors, and human activities on the soil DOC as well as the response mechanisms of the DOC. This review could be helpful to the further understanding of the importance of soil DOC in the carbon cycling of terrestrial ecosystems and the reduction of greenhouse gases emission.

Selection criteria for oxidation method in total organic carbon measurement.

Science.gov (United States)

Yoon, GeunSeok; Park, Sang-Min; Yang, Heuiwon; Tsang, Daniel C W; Alessi, Daniel S; Baek, Kitae

2018-05-01

During the measurement of total organic carbon (TOC), dissolved organic carbon is converted into CO 2 by using high temperature combustion (HTC) or wet chemical oxidation (WCO). However, the criteria for selecting the oxidation methods are not clear. In this study, the chemical structures of organic material were considered as a key factor to select the oxidation method used. Most non-degradable organic compounds showed a similar oxidation efficiency in both methods, including natural organic compounds, dyes, and pharmaceuticals, and thus both methods are appropriate to measure TOC in waters containing these compounds. However, only a fraction of the carbon in the halogenated compounds (perfluorooctanoic acid and trifluoroacetic acid) were oxidized using WCO, resulting in measured TOC values that are considerably lower than those determined by HTC. This result is likely due to the electronegativity of halogen elements which inhibits the approach of electron-rich sulfate radicals in the WCO, and the higher bond strength of carbon-halogen pairs as compared to carbon-hydrogen bonds, which results in a lower degree of oxidation of the compounds. Our results indicate that WCO could be used to oxidize most organic compounds, but may not be appropriate to quantify TOC in organic carbon pools that contain certain halogenated compounds. Copyright © 2018 Elsevier Ltd. All rights reserved.

Stable carbon isotope composition of organic material and carbonate in sediment of a swamp and lakes in Honshu island, Japan

International Nuclear Information System (INIS)

Ishizuka, Toshio

1978-01-01

Recent sediments from a swamp and lakes in Honshu were analyzed for organic carbon and carbonate contents, and stable isotope ratios of carbon in the organic materials and carbonate. delta C 13 values of the carbonate tend to be distinctly larger than those of organic carbon in reducing condition as natural gas field, whereas in oxidizing SO 4 -reducing conditions, they are slightly larger than those of organic carbon within the limited range of a few per mil. Carbon isotopic compositions of organic carbon in sediment of the swamp, Obuchi-numa, were analyzed and compared with habitat analysis of associated fossil diatoms. deltaC 13 values of organic carbon in the sediment vary in correlation with the species abundance in habitat of the associated fossil diatoms, ranging from fresh-water (-0.0282) to coastal marine (-0.0236) via brackish. (auth.)

Fractionation between inorganic and organic carbon during the Lomagundi (2.22 2.1 Ga) carbon isotope excursion

Science.gov (United States)

Bekker, A.; Holmden, C.; Beukes, N. J.; Kenig, F.; Eglinton, B.; Patterson, W. P.

2008-07-01

The Lomagundi (2.22-2.1 Ga) positive carbon isotope excursion in shallow-marine sedimentary carbonates has been associated with the rise in atmospheric oxygen, but subsequent studies have demonstrated that the carbon isotope excursion was preceded by the rise in atmospheric oxygen. The amount of oxygen released to the exosphere during the Lomagundi excursion is constrained by the average global fractionation between inorganic and organic carbon, which is poorly characterized. Because dissolved inorganic and organic carbon reservoirs were arguably larger in the Paleoproterozoic ocean, at a time of lower solar luminosity and lower ocean redox state, decoupling between these two variables might be expected. We determined carbon isotope values of carbonate and organic matter in carbonates and shales of the Silverton Formation, South Africa and in the correlative Sengoma Argillite Formation, near the border in Botswana. These units were deposited between 2.22 and 2.06 Ga along the margin of the Kaapvaal Craton in an open-marine deltaic setting and experienced lower greenschist facies metamorphism. The prodelta to offshore marine shales are overlain by a subtidal carbonate sequence. Carbonates exhibit elevated 13C values ranging from 8.3 to 11.2‰ vs. VPDB consistent with deposition during the Lomagundi positive excursion. The total organic carbon (TOC) contents range from 0.01 to 0.6% and δ13C values range from - 24.8 to - 13.9‰. Thus, the isotopic fractionation between organic and carbonate carbon was on average 30.3 ± 2.8‰ ( n = 32) in the shallow-marine environment. The underlying Sengoma shales have highly variable TOC contents (0.14 to 21.94%) and δ13C values (- 33.7 to - 20.8‰) with an average of - 27.0 ± 3.0‰ ( n = 50). Considering that the shales were also deposited during the Lomagundi excursion, and taking δ13C values of the overlying carbonates as representative of the δ13C value of dissolved inorganic carbon during shale deposition, a carbon

Quality and Quantity of Particulate Organic Carbon in a Coral Reef at Tioman Island, Malaysia

International Nuclear Information System (INIS)

Nakajima, R.; Toda, T.; Shibata, A.

2011-01-01

The quality and quantity of particulate organic carbon (POC) were investigated in a fringing coral reef of Tioman Island, Malaysia to better understand the food sources for reef meso-zooplankton. Phytoplankton biomass in the water column was on average 0.22 (± 0.07) mg Chl-a m-3, of which pico phytoplankton was the most important (size <3 μm, 50-70 % of the total Chl-a). The proportion of C biomass by phytoplankton and other plankton to particulate organic carbon (POC) was low (6 % and 5 %, respectively) and the major portion of POC was occupied by detritus (89 %), suggesting that the diet of particle-feeding or suspension feeding meso-zooplankton would chiefly consist of detritus. (author)

Natural sulfurization of carbohydrates in marine sediments : consequences for the chemical and carbon isotopic composition of sedimentary organic matter

NARCIS (Netherlands)

Dongen, B.E. van

2003-01-01

Carbohydrates make up the largest part of the organic matter in the biosphere and are used by living organism for many different reasons. They serve, among others, as carbon and energy source as well as metabolic intermediates. Carbohydrates are generally thought to be remineralized during early

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

Science.gov (United States)

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.

Thermal hydrolysis of sludge and the use of hydrolysate as carbon source for denitrification

Energy Technology Data Exchange (ETDEWEB)

Barlindhaug, J

1995-10-01

As a consequence of the North Sea- and the Baltic Sea Treaties as well as the Wastewater Directive of the EU, several large wastewater treatment plants discharging to sensitive receiving waters have to include phosphorus as well as nitrogen removal. This thesis evaluates the so called NTH-process for nutrient removal. In this process pre-precipitation is used in front of a biological nitrogen removal step that is based on a combination of pre- and post-denitrification in moving bed biofilm reactors. The biological step is followed by a final separation step, possibly after coagulant addition. Carbon source for the post denitrification step is made available by hydrolysis of the sludge produced. The idea is that the particulate organic matter, which in a traditional pre-denitrification step would have to be enzymatically hydrolyzed, can be more efficiently hydrolyzed in a concentrated sidestream and used in a post-denitrification step. In the thesis hydrolyzed sludge is used as a carbon source for denitrification. The objective is to investigate the influence of varying hydrolysis conditions on the composition and amount of the thermal hydrolysate produced, as well as the quality of the hydrolysate as a carbon source for denitrification. 201 refs., 78 refs., 53 tabs.

Influence of sample composition on aerosol organic and black carbon determinations

Energy Technology Data Exchange (ETDEWEB)

Novakov, T.; Corrigan, C.E.

1995-07-01

In this paper we present results on characterization of filter-collected redwood (Sequoia sempevirens)-needle and eucalyptus smoke particles by thermal, optical, and solvent extraction methods. Our results demonstrate that organic and black carbon concentrations determined by thermal and optical methods are not only method dependent, but also critically influenced by the overall chemical composition of the samples. These conclusions are supported by the following: (1) the organic fraction of biomass smoke particles analyzed includes a component, ranging in concentration from about 6-20% of total carbon or from 16-30% of organic carbon, that is relatively non-volatile and has a combustion temperature close to that of black carbon; (2) presence of K or Na in biomass smoke samples lowers the combustion temperatures of this organic component and of black carbon, making their combustion properties indistinguishable; (3) about 20% of total organic material is nonvolatile when heated to 550{degrees}C in an inert atmosphere. Consequently, thermal methods that rely on a specific temperature to separate organic from black carbon may either underestimate or overestimate the black and organic carbon concentrations, depending on the amounts of Na and K and on the composition and concentration of organic material present in a sample. These analytical uncertainties and, under some conditions, absorption by organic material may contribute to the variability of empirically derived proportionality between light transmission through filter deposits and black carbon concentrations.

Influence of sample composition on aerosol organic and black carbon determinations

International Nuclear Information System (INIS)

Novakov, T.; Corrigan, C.E.

1995-07-01

In this paper we present results on characterization of filter-collected redwood (Sequoia sempevirens)-needle and eucalyptus smoke particles by thermal, optical, and solvent extraction methods. Our results demonstrate that organic and black carbon concentrations determined by thermal and optical methods are not only method dependent, but also critically influenced by the overall chemical composition of the samples. These conclusions are supported by the following: (1) the organic fraction of biomass smoke particles analyzed includes a component, ranging in concentration from about 6-20% of total carbon or from 16-30% of organic carbon, that is relatively non-volatile and has a combustion temperature close to that of black carbon; (2) presence of K or Na in biomass smoke samples lowers the combustion temperatures of this organic component and of black carbon, making their combustion properties indistinguishable; (3) about 20% of total organic material is nonvolatile when heated to 550 degrees C in an inert atmosphere. Consequently, thermal methods that rely on a specific temperature to separate organic from black carbon may either underestimate or overestimate the black and organic carbon concentrations, depending on the amounts of Na and K and on the composition and concentration of organic material present in a sample. These analytical uncertainties and, under some conditions, absorption by organic material may contribute to the variability of empirically derived proportionality between light transmission through filter deposits and black carbon concentrations

Melanised endophytic fungi may increase stores of organic carbon in soil

Science.gov (United States)

McGee, Peter; Mukasa Mugerwa, Tendo

2013-04-01

The processes underlying the carbon cycle in soil, especially sequestration of organic carbon (OC), are poorly understood. Hydrolysis and oxidation reduce organic matter. Hydrolysis degrades linear organic molecules in aerobic and anaerobic conditions, though it is slower in anaerobic conditions. Aromatic compounds are only degraded by oxidation. Oxygen is by far the most common electron acceptor in soil. Anaerobic conditions preclude oxidation in soil and will result in the preservation of aromatic compounds so long as the conditions remain anaerobic. We experimentally tested this model using melanised endophytic fungi. Melanin is a polyaromatic compound that can be readily visualised, though is difficult to quantify. An endophytic association provides the fungus with an ongoing source of energy. Fungal hyphae elongate considerable distances in soil where they may colonise aggregates, the core of which may be anaerobic. The hypothesis we tested is that melanised endophytic fungi increase OC in soil. Seedlings of subterranean clover inoculated with single isolates were grown in split pots where the impact of the fungus could be quantified in the hyphal chamber, separated from the roots by a steel mesh. We found that melanised endophytic fungi significantly increased OC and aromatic carbon in a well-aggregated carbon-rich soil. OC increased by up to 17% within 14 weeks. Twenty out of 24 isolates statistically significantly increased and none decreased OC. Increases differed between fungal isolates. Increases in the hyphal chamber were independent of any change in OC associated with the roots of the host plant. The storage of OC in field soils is being explored. Inoculation of plant roots with melanised endophytic fungi offers one means whereby OC may be increased in field soils.

Driving forces of organic carbon spatial distribution in the tropical seascape

Science.gov (United States)

Gillis, L. G.; Belshe, F. E.; Ziegler, A. D.; Bouma, T. J.

2017-02-01

An important ecosystem service of tropical coastal vegetation including seagrass beds and mangrove forests is their ability to accumulate carbon. Here we attempt to establish the driving forces for the accumulation of surface organic carbon in southern Thailand coastal systems. Across 12 sites we found that in line with expectations, seagrass beds (0.6 ± 0.09%) and mangrove forests (0.9 ± 0.3%) had higher organic carbon in the surface (top 5 cm) sediment than un-vegetated mudflats (0.4 ± 0.04%). Unexpectedly, however, mangrove forests in this region retained organic carbon, rather than outwell it, under normal tidal conditions. No relationship was found between organic carbon and substrate grain size. The most interesting finding of our study was that climax and pioneer seagrass species retained more carbon than mixed-species meadows, suggesting that plant morphology and meadow characteristics can be important factors in organic carbon accumulation. Insights such as these are important in developing carbon management strategies involving coastal ecosystems such as offsetting of carbon emissions. The ability of tropical coastal vegetation to sequester carbon is an important aspect for valuing the ecosystems. Our results provide some initial insight into the factors affecting carbon sequestration in these ecosystems, but also highlight the need for further research on a global scale.

Partitioning Carbon Dioxide Emission and Assessing Dissolved Organic Carbon Leaching of a Drained Peatland Cultivated with Pineapple at Saratok, Malaysia

Directory of Open Access Journals (Sweden)

Liza Nuriati Lim Kim Choo

2014-01-01

Full Text Available Pineapples (Ananas comosus (L. Merr. cultivation on drained peats could affect the release of carbon dioxide (CO2 into the atmosphere and also the leaching of dissolved organic carbon (DOC. Carbon dioxide emission needs to be partitioned before deciding on whether cultivated peat is net sink or net source of carbon. Partitioning of CO2 emission into root respiration, microbial respiration, and oxidative peat decomposition was achieved using a lysimeter experiment with three treatments: peat soil cultivated with pineapple, bare peat soil, and bare peat soil fumigated with chloroform. Drainage water leached from cultivated peat and bare peat soil was also analyzed for DOC. On a yearly basis, CO2 emissions were higher under bare peat (218.8 t CO2 ha/yr than under bare peat treated with chloroform (205 t CO2 ha/yr, and they were the lowest (179.6 t CO2 ha/yr under cultivated peat. Decreasing CO2 emissions under pineapple were attributed to the positive effects of photosynthesis and soil autotrophic activities. An average 235.7 mg/L loss of DOC under bare peat suggests rapid decline of peat organic carbon through heterotrophic respiration and peat decomposition. Soil CO2 emission depended on moderate temperature fluctuations, but it was not affected by soil moisture.

An initial SPARROW model of land use and in-stream controls on total organic carbon in streams of the conterminous United States

Science.gov (United States)

Shih, Jhih-Shyang; Alexander, Richard B.; Smith, Richard A.; Boyer, Elizabeth W.; Shwarz, Grogory E.; Chung, Susie

2010-01-01

Watersheds play many important roles in the carbon cycle: (1) they are a site for both terrestrial and aquatic carbon dioxide (CO2) removal through photosynthesis; (2) they transport living and decomposing organic carbon in streams and groundwater; and (3) they store organic carbon for widely varying lengths of time as a function of many biogeochemical factors. Using the U.S. Geological Survey (USGS) Spatially Referenced Regression on Watershed Attributes (SPARROW) model, along with long-term monitoring data on total organic carbon (TOC), this research quantitatively estimates the sources, transport, and fate of the long-term mean annual load of TOC in streams of the conterminous United States. The model simulations use surrogate measures of the major terrestrial and aquatic sources of organic carbon to estimate the long-term mean annual load of TOC in streams. The estimated carbon sources in the model are associated with four land uses (urban, cultivated, forest, and wetlands) and autochthonous fixation of carbon (stream photosynthesis). Stream photosynthesis is determined by reach-level application of an empirical model of stream chlorophyll based on total phosphorus concentration, and a mechanistic model of photosynthetic rate based on chlorophyll, average daily solar irradiance, water column light attenuation, and reach dimensions. It was found that the estimate of in-stream photosynthesis is a major contributor to the mean annual TOC load per unit of drainage area (that is, yield) in large streams, with a median share of about 60 percent of the total mean annual carbon load in streams with mean flows above 500 cubic feet per second. The interquartile range of the model predictions of TOC from in-stream photosynthesis is from 0.1 to 0.4 grams (g) carbon (C) per square meter (m-2) per day (day-1) for the approximately 62,000 stream reaches in the continental United States, which compares favorably with the reported literature range for net carbon fixation by

Re-establishing marshes can return carbon sink functions to a current carbon source in the Sacramento-San Joaquin Delta of California, USA

Science.gov (United States)

Miller, Robin L.; Fujii, Roger; Schmidt, Paul E.

2011-01-01

. Decomposition rates were related to differences in hydrologic conditions, including water temperature, pH, dissolved oxygen concentration, and availability of alternate electron acceptors. The study showed that marsh re-establishment with permanent, low energy, shallow flooding can limit oxidation of organic soils, thus, effectively turning subsiding land from atmospheric carbon sources to carbon sinks, and at the same time reducing flood vulnerability.

Carbon Sources for Polyhydroxyalkanoates and an Integrated Biorefinery

Directory of Open Access Journals (Sweden)

Guozhan Jiang

2016-07-01

Full Text Available Polyhydroxyalkanoates (PHAs are a group of bioplastics that have a wide range of applications. Extensive progress has been made in our understanding of PHAs’ biosynthesis, and currently, it is possible to engineer bacterial strains to produce PHAs with desired properties. The substrates for the fermentative production of PHAs are primarily derived from food-based carbon sources, raising concerns over the sustainability of their production in terms of their impact on food prices. This paper gives an overview of the current carbon sources used for PHA production and the methods used to transform these sources into fermentable forms. This allows us to identify the opportunities and restraints linked to future sustainable PHA production. Hemicellulose hydrolysates and crude glycerol are identified as two promising carbon sources for a sustainable production of PHAs. Hemicellulose hydrolysates and crude glycerol can be produced on a large scale during various second generation biofuels’ production. An integration of PHA production within a modern biorefinery is therefore proposed to produce biofuels and bioplastics simultaneously. This will create the potential to offset the production cost of biofuels and reduce the overall production cost of PHAs.

Carbon Sources for Polyhydroxyalkanoates and an Integrated Biorefinery.

Science.gov (United States)

Jiang, Guozhan; Hill, David J; Kowalczuk, Marek; Johnston, Brian; Adamus, Grazyna; Irorere, Victor; Radecka, Iza

2016-07-19

Polyhydroxyalkanoates (PHAs) are a group of bioplastics that have a wide range of applications. Extensive progress has been made in our understanding of PHAs' biosynthesis, and currently, it is possible to engineer bacterial strains to produce PHAs with desired properties. The substrates for the fermentative production of PHAs are primarily derived from food-based carbon sources, raising concerns over the sustainability of their production in terms of their impact on food prices. This paper gives an overview of the current carbon sources used for PHA production and the methods used to transform these sources into fermentable forms. This allows us to identify the opportunities and restraints linked to future sustainable PHA production. Hemicellulose hydrolysates and crude glycerol are identified as two promising carbon sources for a sustainable production of PHAs. Hemicellulose hydrolysates and crude glycerol can be produced on a large scale during various second generation biofuels' production. An integration of PHA production within a modern biorefinery is therefore proposed to produce biofuels and bioplastics simultaneously. This will create the potential to offset the production cost of biofuels and reduce the overall production cost of PHAs.

Uncertainty assessment of source attribution of PM(2.5) and its water-soluble organic carbon content using different biomass burning tracers in positive matrix factorization analysis--a case study in Beijing, China.

Science.gov (United States)

Tao, Jun; Zhang, Leiming; Zhang, Renjian; Wu, Yunfei; Zhang, Zhisheng; Zhang, Xiaoling; Tang, Yixi; Cao, Junji; Zhang, Yuanhang

2016-02-01

Daily PM2.5 samples were collected at an urban site in Beijing during four one-month periods in 2009-2010, with each period in a different season. Samples were subject to chemical analysis for various chemical components including major water-soluble ions, organic carbon (OC) and water-soluble organic carbon (WSOC), element carbon (EC), trace elements, anhydrosugar levoglucosan (LG), and mannosan (MN). Three sets of source profiles of PM2.5 were first identified through positive matrix factorization (PMF) analysis using single or combined biomass tracers - non-sea salt potassium (nss-K(+)), LG, and a combination of nss-K(+) and LG. The six major source factors of PM2.5 included secondary inorganic aerosol, industrial pollution, soil dust, biomass burning, traffic emission, and coal burning, which were estimated to contribute 31±37%, 39±28%, 14±14%, 7±7%, 5±6%, and 4±8%, respectively, to PM2.5 mass if using the nss-K(+) source profiles, 22±19%, 29±17%, 20±20%, 13±13%, 12±10%, and 4±6%, respectively, if using the LG source profiles, and 21±17%, 31±18%, 19±19%, 11±12%, 14±11%, and 4±6%, respectively, if using the combined nss-K(+) and LG source profiles. The uncertainties in the estimation of biomass burning contributions to WSOC due to the different choices of biomass burning tracers were around 3% annually and up to 24% seasonally in terms of absolute percentage contributions, or on a factor of 1.7 annually and up to a factor of 3.3 seasonally in terms of the actual concentrations. The uncertainty from the major source (e.g. industrial pollution) was on a factor of 1.9 annually and up to a factor of 2.5 seasonally in the estimated WSOC concentrations. Copyright © 2015 Elsevier B.V. All rights reserved.

Effect of carbon dioxide and bicarbonate as inorganic carbon sources on growth and adaptation of autohydrogenotrophic denitrifying bacteria

International Nuclear Information System (INIS)

Ghafari, Shahin; Hasan, Masitah; Aroua, Mohamed Kheireddine

2009-01-01

Acclimation of autohydrogenotrophic denitrifying bacteria using inorganic carbon source (CO 2 and bicarbonate) and hydrogen gas as electron donor was performed in this study. In this regard, activated sludge was used as the seed source and sequencing batch reactor (SBR) technique was applied for accomplishing the acclimatization. Three distinct strategies in feeding of carbon sources were applied: (I) continuous sparging of CO 2 , (II) bicarbonate plus continuous sparging of CO 2 , and (III) only bicarbonate. The pH-reducing nature of CO 2 showed an unfavorable impact on denitrification rate; however bicarbonate resulted in a buffered environment in the mixed liquor and provided a suitable mean to maintain the pH in the desirable range of 7-8.2. As a result, bicarbonate as the only carbon source showed a faster adaptation, while carbon dioxide as the only carbon source as well as a complementary carbon source added to bicarbonate resulted in longer acclimation period. Adapted hydrogenotrophic denitrifying bacteria, using bicarbonate and hydrogen gas in the aforementioned pH range, caused denitrification at a rate of 13.33 mg NO 3 - -N/g MLVSS/h for degrading 20 and 30 mg NO 3 - -N/L and 9.09 mg NO 3 - -N/g MLVSS/h for degrading 50 mg NO 3 - -N/L

Extraordinary slow degradation of dissolved organic carbon (DOC) in a cold marginal sea.

Science.gov (United States)

Kim, Tae-Hoon; Kim, Guebuem; Lee, Shin-Ah; Dittmar, Thorsten

2015-09-08

Dissolved organic carbon (DOC) is the largest organic carbon reservoir in the ocean, and the amount of carbon in this reservoir rivals that in atmospheric CO2. In general, DOC introduced into the deep ocean undergoes a significant degradation over a centennial time scale (i.e., ~50 μM to ~34 μM in the North Atlantic and Mediterranean Sea). However, we here show that high concentrations of DOC (58 ± 4 μM) are maintained almost constantly over 100 years in the entire deep East/Japan Sea (EJS). The degradation rate in this sea is estimated to be 0.04 μmol C kg(-1) yr(-1), which is 2-3 times lower than that in the North Atlantic and Mediterranean Sea. Since the source of DOC in the deep EJS is found to be of marine origin on the basis of δ(13)C-DOC signatures, this slow degradation rate seems to be due to low temperature (DOC in the world ocean is very sensitive to global warming and slowdown of global deep-water overturning.

Source apportionment of carbonaceous aerosol in southern Sweden

Directory of Open Access Journals (Sweden)

J. Genberg

2011-11-01

Full Text Available A one-year study was performed at the Vavihill background station in southern Sweden to estimate the anthropogenic contribution to the carbonaceous aerosol. Weekly samples of the particulate matter PM₁₀ were collected on quartz filters, and the amounts of organic carbon, elemental carbon, radiocarbon (¹⁴C and levoglucosan were measured. This approach enabled source apportionment of the total carbon in the PM₁₀ fraction using the concentration ratios of the sources. The sources considered in this study were emissions from the combustion of fossil fuels and biomass, as well as biogenic sources. During the summer, the carbonaceous aerosol mass was dominated by compounds of biogenic origin (80%, which are associated with biogenic primary and secondary organic aerosols. During the winter months, biomass combustion (32% and fossil fuel combustion (28% were the main contributors to the carbonaceous aerosol. Elemental carbon concentrations in winter were about twice as large as during summer, and can be attributed to biomass combustion, probably from domestic wood burning. The contribution of fossil fuels to elemental carbon was stable throughout the year, although the fossil contribution to organic carbon increased during the winter. Thus, the organic aerosol originated mainly from natural sources during the summer and from anthropogenic sources during the winter. The result of this source apportionment was compared with results from the EMEP MSC-W chemical transport model. The model and measurements were generally consistent for total atmospheric organic carbon, however, the contribution of the sources varied substantially. E.g. the biomass burning contributions of OC were underestimated by the model by a factor of 2.2 compared to the measurements.

A linear solvation energy relationship model of organic chemical partitioning to dissolved organic carbon.

Science.gov (United States)

Kipka, Undine; Di Toro, Dominic M

2011-09-01

Predicting the association of contaminants with both particulate and dissolved organic matter is critical in determining the fate and bioavailability of chemicals in environmental risk assessment. To date, the association of a contaminant to particulate organic matter is considered in many multimedia transport models, but the effect of dissolved organic matter is typically ignored due to a lack of either reliable models or experimental data. The partition coefficient to dissolved organic carbon (K(DOC)) may be used to estimate the fraction of a contaminant that is associated with dissolved organic matter. Models relating K(DOC) to the octanol-water partition coefficient (K(OW)) have not been successful for many types of dissolved organic carbon in the environment. Instead, linear solvation energy relationships are proposed to model the association of chemicals with dissolved organic matter. However, more chemically diverse K(DOC) data are needed to produce a more robust model. For humic acid dissolved organic carbon, the linear solvation energy relationship predicts log K(DOC) with a root mean square error of 0.43. Copyright © 2011 SETAC.

[Effects of climate change on forest soil organic carbon storage: a review].

Science.gov (United States)

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.

Aged dissolved organic carbon exported from rivers of the Tibetan Plateau.

Science.gov (United States)

Qu, Bin; Sillanpää, Mika; Li, Chaoliu; Kang, Shichang; Stubbins, Aron; Yan, Fangping; Aho, Kelly Sue; Zhou, Feng; Raymond, Peter A

2017-01-01

The role played by river networks in regional and global carbon cycle is receiving increasing attention. Despite the potential of radiocarbon measurements (14C) to elucidate sources and cycling of different riverine carbon pools, there remain large regions such as the climate-sensitive Tibetan Plateau for which no data are available. Here we provide new 14C data on dissolved organic carbon (DOC) from three large Asian rivers (the Yellow, Yangtze and Yarlung Tsangpo Rivers) running on the Tibetan Plateau and present the carbon transportation pattern in rivers of the plateau versus other river system in the world. Despite higher discharge rates during the high flow season, the DOC yield of Tibetan Plateau rivers (0.41 gC m-2 yr-1) was lower than most other rivers due to lower concentrations. Radiocarbon ages of the DOC were older/more depleted (511±294 years before present, yr BP) in the Tibetan rivers than those in Arctic and tropical rivers. A positive correlation between radiocarbon age and permafrost watershed coverage was observed, indicating that 14C-deplted/old carbon is exported from permafrost regions of the Tibetan Plateau during periods of high flow. This is in sharp contrast to permafrost regions of the Arctic which export 14C-enriched carbon during high discharge periods.

Molecular mechanisms behind the adjustment of phototrophic light-harvesting and mixotrophic utilization of cellulosic carbon sources in Chlamydomonas reinhardtii

OpenAIRE

Blifernez-Klassen, Olga

2012-01-01

Plants, green algae and cyanobacteria perform photosynthetic conversion of sunlight into chemical energy in a permanently changing natural environment, where the efficient utilization of light and inorganic carbon represent the most critical factors. Photosynthetic organisms have developed different acclimation strategies to adapt changing light conditions and insufficient carbon source supply in order to survive and to assure optimal growth and protection. This thesis provides further insigh...

Tracing estuarine organic matter sources into the southern North Sea using C and N isotopic signatures

DEFF Research Database (Denmark)

Bristow, Laura A.; Jickells, Timothy D.; Weston, Keith

2013-01-01

Sources and distribution of particulate organic matter in surface waters of the Humber and Thames estuaries and in the East Anglian plume in the southern North Sea were investigated in winter 2006/2007. Carbon (C) and nitrogen (N) stable isotopes provided evidence for the presence of three partic...

Biomarker and carbon isotope constraints (δ{sup 13}C, Δ{sup 14}C) on sources and cycling of particulate organic matter discharged by large Siberian rivers draining permafrost areas

Energy Technology Data Exchange (ETDEWEB)

Winterfeld, Maria

2014-08-15

Circumpolar permafrost soils store about half of the global soil organic carbon pool. These huge amounts of organic matter (OM) could accumulate due to low temperatures and water saturated soil conditions over the course of millennia. Currently most of this OM remains frozen and therefore does not take part in the active carbon cycle, making permafrost soils a globally important carbon sink. Over the last decades mean annual air temperatures in the Arctic increased stronger than the global mean and this trend is projected to continue. As a result the permafrost carbon pool is under climate pressure possibly creating a positive climate feedback due to the thaw-induced release of greenhouse gases to the atmosphere. Arctic warming will lead to increased annual permafrost thaw depths and Arctic river runoff likely resulting in enhanced mobilization and export of old, previously frozen soil-derived OM. Consequently, the great arctic rivers play an important role in global biogeochemical cycles by connecting the large permafrost carbon pool of their hinterlands with the arctic shelf seas and the Arctic Ocean. The first part of this thesis deals with particulate organic matter (POM) from the Lena Delta and adjacent Buor Khaya Bay. The Lena River in central Siberia is one of the major pathways translocating terrestrial OM from its southernmost reaches near Lake Baikal to the coastal zone of the Laptev Sea. The permafrost soils from the Lena catchment area store huge amounts of pre-aged OM, which is expected to be remobilized due to climate warming. To characterize the composition and vegetation sources of OM discharged by the Lena River, the lignin phenol and carbon isotopic composition (δ{sup 13}C and Δ{sup 14}C) in total suspended matter (TSM) from surface waters, surface sediments from the Buor Khaya Bay along with soils from the Lena Delta's first (Holocene) and third terraces (Pleistocene ice complex) were analyzed. The lignin compositions of these samples are

Middle Holocene Organic Carbon and Biomarker Records from the South Yellow Sea: Relationship to the East Asian Monsoon

Science.gov (United States)

Zou, Liang; Hu, Bangqi; Li, Jun; Dou, Yanguang; Xie, Luhua; Dong, Liang

2018-03-01

The East Asian monsoon system influences the sedimentation and transport of organic matter in East Asian marginal seas that is derived from both terrestrial and marine sources. In this study, we determined organic carbon (OC) isotope values, concentrations of marine biomarkers, and levels of OC and total nitrogen (TN) in core YSC-1 from the central South Yellow Sea (SYS). Our objectives were to trace the sources of OC and variations in palaeoproductivity since the middle Holocene, and their relationships with the East Asian monsoon system. The relative contributions of terrestrial versus marine organic matter in core sediments were estimated using a two-end-member mixing model of OC isotopes. Results show that marine organic matter has been the main sediment constituent since the middle Holocene. The variation of terrestrial organic carbon concentration (OCter) is similar to the EASM history. However, the variation of marine organic carbon concentration (OCmar) is opposite to that of the EASM curve, suggesting OCmar is distinctly influenced by terrestrial material input. Inputs of terrestrial nutrients into the SYS occur in the form of fluvial and aeolian dust, while concentrations of nutrients in surface water are derived mainly from bottom water via the Yellow Sea circulation system, which is controlled by the East Asian winter monsoon (EAWM). Variations in palaeoproductivity represented by marine organic matter and biomarker records are, in general, consistent with the recent EAWM intensity studies, thus, compared with EASM, EAWM may play the main role to control the marine productivity variations in the SYS.

A shift of thermokarst lakes from carbon sources to sinks during the Holocene epoch

Science.gov (United States)

Walter Anthony, K. M.; Zimov, S. A.; Grosse, G.; Jones, Miriam C.; Anthony, P.; Chapin, F. S.; Finlay, J. C.; Mack, M. C.; Davydov, S.; Frenzel, P.F.; Frolking, S.

2014-01-01

Thermokarst lakes formed across vast regions of Siberia and Alaska during the last deglaciation and are thought to be a net source of atmospheric methane and carbon dioxide during the Holocene epoch1,2,3,4. However, the same thermokarst lakes can also sequester carbon5, and it remains uncertain whether carbon uptake by thermokarst lakes can offset their greenhouse gas emissions. Here we use field observations of Siberian permafrost exposures, radiocarbon dating and spatial analyses to quantify Holocene carbon stocks and fluxes in lake sediments overlying thawed Pleistocene-aged permafrost. We find that carbon accumulation in deep thermokarst-lake sediments since the last deglaciation is about 1.6 times larger than the mass of Pleistocene-aged permafrost carbon released as greenhouse gases when the lakes first formed. Although methane and carbon dioxide emissions following thaw lead to immediate radiative warming, carbon uptake in peat-rich sediments occurs over millennial timescales. We assess thermokarst-lake carbon feedbacks to climate with an atmospheric perturbation model and find that thermokarst basins switched from a net radiative warming to a net cooling climate effect about 5,000 years ago. High rates of Holocene carbon accumulation in 20 lake sediments (47±10 grams of carbon per square metre per year; mean±standard error) were driven by thermokarst erosion and deposition of terrestrial organic matter, by nutrient release from thawing permafrost that stimulated lake productivity and by slow decomposition in cold, anoxic lake bottoms. When lakes eventually drained, permafrost formation rapidly sequestered sediment carbon. Our estimate of about 160petagrams of Holocene organic carbon in deep lake basins of Siberia and Alaska increases the circumpolar peat carbon pool estimate for permafrost regions by over 50 per cent (ref. 6). The carbon in perennially frozen drained lake sediments may become vulnerable to mineralization as permafrost disappears7

Increased losses of organic carbon and destabilising of tropical peatlands following deforestation, drainage and burning. (Invited)

Science.gov (United States)

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

2013-12-01

Tropical peatlands contain one of the largest pools of terrestrial organic carbon, amounting to about 89,000 teragrams. Approximately 65% of this carbon store is in Indonesia, where extensive anthropogenic degradation in the form of deforestation, drainage and associated fire is converting it into a globally significant source of atmospheric carbon dioxide. Unlike boreal and temperate forests and higher-latitude wetlands, however, the loss of fluvial organic carbon from tropical peats has yet to be fully quantified. Here, we present the first data from intact and degraded peat swamp forest (PSF) catchments in Central Kalimantan, Borneo, that indicate a doubling of fluvial organic carbon losses from tropical peatlands following deforestation and drainage. Through carbon-14 dating of dissolved organic carbon (DO14C), we find that leaching of DOC from intact PSF is derived mainly from recent primary production. In contrast, DOC from disturbed PSF consists mostly of much older carbon from deep within the peat column. When we include this fluvial carbon loss, which is often ignored in peatland carbon budgets, we find that it increases the estimate of total carbon lost from the disturbed peatlands in our study by 22%. We further estimate that since 1990, peatland disturbance has resulted in a 32% increase in fluvial organic carbon flux from Southeast Asia - an increase that equates to more than half of the entire annual fluvial organic carbon flux from all European peatlands. Finally, we monitored fluvial organic carbon fluxes following large-scale peatland fires in 2009/10 within the study sub-catchments and found fluvial carbon fluxes to be 30-70% larger in the fire-affected catchments when compared to fluxes during the same interval in the previous year (pre-fire). This is in marked contrast to the intact catchment (control/no fire) where there were no differences observed in fluxes 'pre to post fire years'. Our sub-catchment findings were also found to be

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

Directory of Open Access Journals (Sweden)

C. Wu

2016-05-01

Full Text Available 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 / ECpri 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 / ECpri determination. We examine here a method that derives (OC / ECpri through calculating a hypothetical set of (OC / ECpri and SOC followed by seeking the minimum of the coefficient of correlation (R2 between SOC and EC. The hypothetical (OC / ECpri that generates the minimum R2(SOC,EC then represents the actual (OC / ECpri ratio if variations of EC and SOC are independent and (OC / ECpri is relatively constant in the study period. This Minimum R Squared (MRS method has a clear quantitative criterion for the (OC / ECpri 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�

Radiocarbon in marine dissolved organic carbon (DOC)

NARCIS (Netherlands)

Clercq, M. le; Plicht, J. van der; Meijer, H.A.J.; Baar, H.J.W. de

Dissolved Organic Carbon (DOC) plays an important role in the ecology and carbon cycle in the ocean. Analytical problems with concentration and isotope ratio measurements have hindered its study. We have constructed a new analytical method based on supercritical oxidation for the determination of

Time-resolved analysis of particle emissions from residential biomass combustion - Emissions of refractory black carbon, PAHs and organic tracers

Science.gov (United States)

Nielsen, Ingeborg E.; Eriksson, Axel C.; Lindgren, Robert; Martinsson, Johan; Nyström, Robin; Nordin, Erik Z.; Sadiktsis, Ioannis; Boman, Christoffer; Nøjgaard, Jacob K.; Pagels, Joakim

2017-09-01

Time-resolved particle emissions from a conventional wood stove were investigated with aerosol mass spectrometry to provide links between combustion conditions, emission factors, mixing state of refractory black carbon and implications for organic tracer methods. The addition of a new batch of fuel results in low temperature pyrolysis as the fuel heats up, resulting in strong, short-lived, variable emission peaks of organic aerosol-containing markers of anhydrous sugars, such as levoglucosan (fragment at m/z 60). Flaming combustion results in emissions dominated by refractory black carbon co-emitted with minor fractions of organic aerosol and markers of anhydrous sugars. Full cycle emissions are an external mixture of larger organic aerosol-dominated and smaller thinly coated refractory black carbon particles. A very high burn rate results in increased full cycle mass emission factors of 66, 2.7, 2.8 and 1.3 for particulate polycyclic aromatic hydrocarbons, refractory black carbon, total organic aerosol and m/z 60, respectively, compared to nominal burn rate. Polycyclic aromatic hydrocarbons are primarily associated with refractory black carbon-containing particles. We hypothesize that at very high burn rates, the central parts of the combustion zone become air starved, leading to a locally reduced combustion temperature that reduces the conversion rates from polycyclic aromatic hydrocarbons to refractory black carbon. This facilitates a strong increase of polycyclic aromatic hydrocarbons emissions. At nominal burn rates, full cycle emissions based on m/z 60 correlate well with organic aerosol, refractory black carbon and particulate matter. However, at higher burn rates, m/z 60 does not correlate with increased emissions of polycyclic aromatic hydrocarbons, refractory black carbon and organic aerosol in the flaming phase. The new knowledge can be used to advance source apportionment studies, reduce emissions of genotoxic compounds and model the climate impacts of

Effect of carbon dioxide and bicarbonate as inorganic carbon sources on growth and adaptation of autohydrogenotrophic denitrifying bacteria

Energy Technology Data Exchange (ETDEWEB)

Ghafari, Shahin; Hasan, Masitah [Department of Chemical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia); Aroua, Mohamed Kheireddine [Department of Chemical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia)], E-mail: mk_aroua@um.edu.my

2009-03-15

Acclimation of autohydrogenotrophic denitrifying bacteria using inorganic carbon source (CO{sub 2} and bicarbonate) and hydrogen gas as electron donor was performed in this study. In this regard, activated sludge was used as the seed source and sequencing batch reactor (SBR) technique was applied for accomplishing the acclimatization. Three distinct strategies in feeding of carbon sources were applied: (I) continuous sparging of CO{sub 2}, (II) bicarbonate plus continuous sparging of CO{sub 2}, and (III) only bicarbonate. The pH-reducing nature of CO{sub 2} showed an unfavorable impact on denitrification rate; however bicarbonate resulted in a buffered environment in the mixed liquor and provided a suitable mean to maintain the pH in the desirable range of 7-8.2. As a result, bicarbonate as the only carbon source showed a faster adaptation, while carbon dioxide as the only carbon source as well as a complementary carbon source added to bicarbonate resulted in longer acclimation period. Adapted hydrogenotrophic denitrifying bacteria, using bicarbonate and hydrogen gas in the aforementioned pH range, caused denitrification at a rate of 13.33 mg NO{sub 3}{sup -}-N/g MLVSS/h for degrading 20 and 30 mg NO{sub 3}{sup -}-N/L and 9.09 mg NO{sub 3}{sup -}-N/g MLVSS/h for degrading 50 mg NO{sub 3}{sup -}-N/L.

Organic and inorganic carbon dynamics in a karst aquifer: Santa Fe River Sink-Rise system, north Florida, USA

Science.gov (United States)

Jin, Jin; Zimmerman, Andrew R.; Moore, Paul J.; Martin, Jonathan B.

2014-03-01

Spatiotemporal variations in dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), major ions concentrations and other geochemical parameters including stable carbon isotopes of DIC (δ13CDIC), were measured in surface water and deep and shallow well water samples of the Santa Fe River Sink-Rise eogenetic karst system, north Florida, USA. Three end-member water sources were identified: one DOC-rich/DIC-poor/δ13CDIC-depleted, one DOC-poor/DIC-rich/δ13CDIC-enriched, and one enriched in major ions. Given their spatiotemporal distributions, they were presumed to represent soil water, upper aquifer groundwater, and deep aquifer water sources, respectively. Using assumed ratios of Na+, Cl, and SO42- for each end-member, a mixing model calculated the contribution of each water source to each sample. Then, chemical effects of biogeochemical reactions were calculated as the difference between those predicted by the mixing model and measured species concentrations. In general, carbonate mineral dissolution occurred throughout the Sink-Rise system, surface waters were net autotrophic and the subsurface was in metabolic balance, i.e., no net DOC or DIC production or consumption. However, there was evidence for chemolithoautotrophy, perhaps by hydrogen oxidizing microbes, at some deep aquifer sites. Mineralization of this autochthonous natural dissolved organic matter (NDOM) led to localized carbonate dissolution as did surface water-derived NDOM supplied to shallow well sites during the highest flow periods. This study demonstrates linkages between hydrology, abiotic and microbial processes and carbon dynamics and has important implications for groundwater quality, karst morphologic evolution, and hydrogeologic projects such as aquifer storage and recovery in karst systems.

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

Science.gov (United States)

Xu, Xiaoming; Zhu, Qing; Zhou, Qianzhi; Liu, Jinzhong; Yuan, Jianping; Wang, Jianghai

2018-01-01

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

Organic carbon amendments for passive in situ treatment of mine drainage: Field experiments

Energy Technology Data Exchange (ETDEWEB)

Lindsay, Matthew B.J., E-mail: mbjlindsay@uwaterloo.ca [Department of Earth and Environmental Sciences, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, N2L 3G1 (Canada); Blowes, David W.; Condon, Peter D.; Ptacek, Carol J. [Department of Earth and Environmental Sciences, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, N2L 3G1 (Canada)

2011-07-15

Highlights: > Organic carbon amendments can support passive treatment of mine drainage. > Decreased transport of sulfide-oxidation products under sulfate-reducing conditions. > Treatment effectiveness dependent on organic carbon source and amendment rate. - Abstract: A field-scale experiment was conducted to evaluate various organic C sources as amendments for passive treatment of tailings pore water. Varied mixtures of peat, spent-brewing grain (SBG) and municipal biosolids (MB) were assessed for the potential to promote dissimilatory sulfate reduction (DSR) and metal-sulfide precipitation. Five amended cells and one control were constructed in the vadose zone of a sulfide- and carbonate-rich tailings deposit, and the geochemistry, microbiology and mineralogy were monitored for 4 a. Increases in pore-water concentrations of dissolved organic C (DOC) and decreases in aqueous SO{sub 4} concentrations of >2500 mg L{sup -1} were observed in cells amended with peat + SBG and peat + SBG + MB. Removal of SO{sub 4} was accompanied by shifts in {delta}{sup 34}S-SO{sub 4} values of >+30 per mille, undersaturation of pore water with respect to gypsum [CaSO{sub 4}.2H{sub 2}O], and increased populations of SO{sub 4}-reducing bacteria (SRB). Decreases in aqueous concentrations of Zn, Mn, Ni, Sb and Tl were observed for these cells relative to the control. Organic C introduction also supported growth of Fe-reducing bacteria (IRB) and increases in Fe and As concentrations. Enhanced Fe and As mobility occurred in all cells; however, maximum concentrations were observed in cells amended with MB. Subsequent decreases in Fe and As concentrations were attributed to DSR and metal-sulfide precipitation. The common presence of secondary Zn-S and Fe-S phases was observed by field emission-scanning electron microscopy (FE-SEM) and energy dispersive X-ray (EDS) spectroscopy. Selective extractions indicated that large decreases in water-soluble SO{sub 4} occurred in cells that supported DSR

Organic carbon amendments for passive in situ treatment of mine drainage: Field experiments

International Nuclear Information System (INIS)

Lindsay, Matthew B.J.; Blowes, David W.; Condon, Peter D.; Ptacek, Carol J.

2011-01-01

Highlights: → Organic carbon amendments can support passive treatment of mine drainage. → Decreased transport of sulfide-oxidation products under sulfate-reducing conditions. → Treatment effectiveness dependent on organic carbon source and amendment rate. - Abstract: A field-scale experiment was conducted to evaluate various organic C sources as amendments for passive treatment of tailings pore water. Varied mixtures of peat, spent-brewing grain (SBG) and municipal biosolids (MB) were assessed for the potential to promote dissimilatory sulfate reduction (DSR) and metal-sulfide precipitation. Five amended cells and one control were constructed in the vadose zone of a sulfide- and carbonate-rich tailings deposit, and the geochemistry, microbiology and mineralogy were monitored for 4 a. Increases in pore-water concentrations of dissolved organic C (DOC) and decreases in aqueous SO 4 concentrations of >2500 mg L -1 were observed in cells amended with peat + SBG and peat + SBG + MB. Removal of SO 4 was accompanied by shifts in δ 34 S-SO 4 values of >+30 per mille, undersaturation of pore water with respect to gypsum [CaSO 4 .2H 2 O], and increased populations of SO 4 -reducing bacteria (SRB). Decreases in aqueous concentrations of Zn, Mn, Ni, Sb and Tl were observed for these cells relative to the control. Organic C introduction also supported growth of Fe-reducing bacteria (IRB) and increases in Fe and As concentrations. Enhanced Fe and As mobility occurred in all cells; however, maximum concentrations were observed in cells amended with MB. Subsequent decreases in Fe and As concentrations were attributed to DSR and metal-sulfide precipitation. The common presence of secondary Zn-S and Fe-S phases was observed by field emission-scanning electron microscopy (FE-SEM) and energy dispersive X-ray (EDS) spectroscopy. Selective extractions indicated that large decreases in water-soluble SO 4 occurred in cells that supported DSR. Furthermore, amendments that supported

High resolution of black carbon and organic carbon emissions in the Pearl River Delta region, China.

Science.gov (United States)

Zheng, Junyu; He, Min; Shen, Xingling; Yin, Shasha; Yuan, Zibing

2012-11-01

A high-resolution regional black carbon (BC) and organic carbon (OC) emission inventory for the year 2009 was developed for the Pearl River Delta (PRD) region, China, based on the collected activity data and the latest emission factors. PM(2.5), BC and OC emissions were estimated to be 303 kt, 39 kt and 31 kt, respectively. Industrial processes were major contributing sources to PM(2.5) emissions. BC emissions were mainly from mobile sources, accounting for 65.0%, while 34.1% of OC emissions were from residential combustion. The primary OC/BC ratios for individual cities in the PRD region were dependent on the levels of economic development due to differences in source characteristics, with high ratios in the less developed cities and low ratios in the central and southern developed areas. The preliminary temporal profiles were established, showing the highest OC emissions in winter and relatively constant BC emissions throughout the year. The emissions were spatially allocated into grid cells with a resolution of 3 km × 3 km. Large amounts of BC emissions were distributed over the central-southern PRD city clusters, while OC emissions exhibited a relatively even spatial distribution due to the significant biomass burning emissions from the outlying area of the PRD region. Uncertainties in carbonaceous aerosol emissions were usually higher than in other primary pollutants like SO(2), NO(x), and PM(10). One of the key uncertainty sources was the emission factor, due to the absence of direct measurements of BC and OC emission rates. Copyright © 2012 Elsevier B.V. All rights reserved.

Soil Organic Carbon dynamics in agricultural soils of Veneto Region

Science.gov (United States)

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

Method for obtaining more precise measures of excreted organic carbon

International Nuclear Information System (INIS)

Anon.

1977-01-01

A new method for concentrating and measuring excreted organic carbon by lyophilization and scintillation counting is efficient, improves measurable radioactivity, and increases precision for estimates of organic carbon excreted by phytoplankton and macrophytes

Adsorption of volatile organic compounds by pecan shell- and almond shell-based granular activated carbons.

Science.gov (United States)

Bansode, R R; Losso, J N; Marshall, W E; Rao, R M; Portier, R J

2003-11-01

The objective of this research was to determine the effectiveness of using pecan and almond shell-based granular activated carbons (GACs) in the adsorption of volatile organic compounds (VOCs) of health concern and known toxic compounds (such as bromo-dichloromethane, benzene, carbon tetrachloride, 1,1,1-trichloromethane, chloroform, and 1,1-dichloromethane) compared to the adsorption efficiency of commercially used carbons (such as Filtrasorb 200, Calgon GRC-20, and Waterlinks 206C AW) in simulated test medium. The pecan shell-based GACs were activated using steam, carbon dioxide or phosphoric acid. An almond shell-based GAC was activated with phosphoric acid. Our results indicated that steam- or carbon dioxide-activated pecan shell carbons were superior in total VOC adsorption to phosphoric acid-activated pecan shell or almond shell carbons, inferring that the method of activation selected for the preparation of activated carbons affected the adsorption of VOCs and hence are factors to be considered in any adsorption process. The steam-activated, pecan shell carbon adsorbed more total VOCs than the other experimental carbons and had an adsorption profile similar to the two coconut shell-based commercial carbons, but had greater adsorption than the coal-based commercial carbon. All the carbons studied adsorbed benzene more effectively than the other organics. Pecan shell, steam-activated and acid-activated GACs showed higher adsorption of 1,1,1-trichloroethane than the other carbons studied. Multivariate analysis was conducted to group experimental carbons and commercial carbons based on their physical, chemical, and adsorptive properties. The results of the analysis conclude that steam-activated and acid-activated pecan shell carbons clustered together with coal-based and coconut shell-based commercial carbons, thus inferring that these experimental carbons could potentially be used as alternative sources for VOC adsorption in an aqueous environment.

Stable isotope (δ"1"3C and δ"1"5N) based interpretation of organic matter source and paleoenvironmental conditions in Al-Azraq basin, Jordan

International Nuclear Information System (INIS)

Ahmad, Khaldoun; Davies, Caroline

2017-01-01

This study examines the stable isotopes of carbon and nitrogen from cored lacustrine sediments of the Al-Azraq, an arid lake basin on the Jordan Plateau. Lacustrine sediments contain valuable records of paleoenvironmental conditions, recording local and regional responses to environmental change. Previous paleo-reconstructions on the Jordan Plateau are based on archaeology, pollen, mineralogy, and stratigraphy. The application of organic geochemistry analyses to these lake sediments identifies multiple sources of organic matter, biological production, and contributes to understanding the paleoenvironments of the Al-Azraq basin during the mid-Pleistocene period. Organic carbon concentration (Corg) provides an overview of the organic matter distribution. Carbon isotopic composition (δ13Corg) and nitrogen isotopic composition (δ15N) are indicators of organic matter sources and paleoproductivity. Magnetic susceptibility (MGSUS) measured the concentration of ferromagnetic minerals and indicated aeolian inputs. Organic geochemistry differentiated five paleoenvironmental zones with specific sources of organic matter, both aquatic and terrestrial. It identified a long period of climate wetter than the present, punctuated by a short intense period of aridity. Diagenesis plays an important role in the decomposition of organic matter and studies indicate this degradation can alter the isotopic signals of organic matter. Analyses of the isotopic signals and statistical analyses demonstrate diagenesis is not a factor in the Al-Azraq sediments in all but Zone 4 of the paleoenvironmental zones. This Zone is defined by less negative carbon isotopic composition and the presence of thick primary gypsum layers, in addition to the influx of high peaks of aeolian sediment as reflected in the magnetic susceptibility data. Stable isotope geochemistry provides detailed information on the paleoenvironments of lake sediments, and is applicable to typically challenging arid basin sediments

The source and distribution of thermogenic dissolved organic matter in the ocean

Science.gov (United States)

Dittmar, T.; Suryaputra, I. G. N. A.; Paeng, J.

2009-04-01

Thermogenic organic matter (ThOM) is abundant in the environment. ThOM is produced at elevated temperature and pressure in deep sediments and earth's crust, and it is also a residue of fossil fuel and biomass burning ("black carbon"). Because of its refractory character, it accumulates in soils and sediments and, therefore, may sequester carbon from active cycles. It was hypothesized that a significant component of marine dissolved organic matter (DOM) might be thermogenic. Here we present a detailed data set on the distribution of thermogenic DOM in major water masses of the deep and surface ocean. In addition, several potential sources of thermogenic DOM to the ocean were investigated: active seeps of brine fluids in the deep Gulf of Mexico, rivers, estuaries and submarine groundwaters. Studies on deep-sea hydrothermal vents and aerosol deposition are ongoing. All DOM samples were isolated from seawater via solid phase extraction (SPE-DOM). ThOM was quantified in the extracts as benzene-polycarboxylic acids (BPCAs) after nitric acid oxidation via high-performance liquid chromatography and diode array detection (HPLC-DAD). BPCAs are produced exclusively from fused ring systems and are therefore unambiguous molecular tracers for ThOM. In addition to BPCA determination, the molecular composition and structure of ThOM was characterized in detail via ultrahigh resolution mass spectrometry (FT-ICR-MS). All marine and river DOM samples yielded significant amounts of BPCAs. The cold seep system in the deep Gulf of Mexico, but also black water rivers (like the Suwannee River) were particularly rich in ThOM. Up to 10% of total dissolved organic carbon was thermogenic in both systems. The most abundant BPCA was benzene-pentacarboxylic acid (B5CA). The molecular composition of BPCAs and the FT-ICR-MS data indicate a relatively small number (5-8) of fused aromatic rings per molecule. Overall, the molecular BPCA patterns were very similar independent of the source of Th

Redox-controlled carbon and phosphorus burial: A mechanism for enhanced organic carbon sequestration during the PETM

Science.gov (United States)

Komar, Nemanja; Zeebe, Richard E.

2017-12-01

Geological records reveal a major perturbation in carbon cycling during the Paleocene-Eocene Thermal Maximum (PETM, ∼56 Ma), marked by global warming of more than 5 °C and a prominent negative carbon isotope excursion of at least 2.5‰ within the marine realm. The entire event lasted about 200,000 yr and was associated with a massive release of light carbon into the ocean-atmosphere system over several thousands of years. Here we focus on the terminal stage of the PETM, during which the ocean-atmosphere system rapidly recovered from the carbon cycle perturbation. We employ a carbon-cycle box model to examine the feedbacks between surface ocean biological production, carbon, oxygen, phosphorus, and carbonate chemistry during massive CO2 release events, such as the PETM. The model results indicate that the redox-controlled carbon-phosphorus feedback is capable of producing enhanced organic carbon sequestration during large carbon emission events. The locale of carbon oxidation (ocean vs. atmosphere) does not affect the amount of carbon sequestered. However, even though the model produces trends consistent with oxygen, excess accumulation rates of organic carbon (∼1700 Pg C during the recovery stage), export production and δ13 C data, it fails to reproduce the magnitude of change of sediment carbonate content and the CCD over-deepening during the recovery stage. The CCD and sediment carbonate content overshoot during the recovery stage is muted by a predicted increase in CaCO3 rain. Nonetheless, there are indications that the CaCO3 export remained relatively constant during the PETM. If this was indeed true, then an initial pulse of 3,000 Pg C followed by an additional, slow leak of 2,500 Pg C could have triggered an accelerated nutrient supply to the surface ocean instigating enhanced organic carbon export, consequently increasing organic carbon sequestration, resulting in an accelerated restoration of ocean-atmosphere biogeochemistry during the termination

Examining organic carbon transport by the Orinoco River using SeaWiFS imagery

Science.gov (United States)

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.

Fate of the herbicide glufosinate-ammonium in the sandy, low-organic-carbon aquifer at CFB Borden, Ontario, Canada

Science.gov (United States)

Allen-King, Richelle M.; Butler, Barbara J.; Reichert, Barbara

1995-04-01

The herbicide glufosinate-ammonium was persistent in aerobic sandy aquifer material in laboratory batch and field in situ microcosms when added at concentrations of 50-400 μg L -1. In contrast, the compound is biotransformed relatively quickly in surface soil. Glufosinate transformation and metabolite (3-methylphosphinyl-propionic acid) production in carbonamended laboratory microcosms demonstrated that the aquifer system was carbon-limited with respect to glufosinate transformation. Microbiological test showed that flufosinateammonium and sodium-glufosinate was be used as a nitrogen source, in the presence of sufficient carbon. Glufosinate was not used by the native microorganisms as a source of phosphorus, nor metabolized as a sole carbon and energy source. Ammonium appeared to be preferred over glufosinate as a nitrogen source. When representative microbial strains isolated from the Borden aquifer were tested, most were glufosinate-ammonium tolerant. Complete inhibition of some isolates was demonstrated only at very high concentrations of 2-4 g L -1. The research suggests that in an aquifer with a relatively low clay content and little labile organic carbon, such as the sandy aquifer at the field site, glufosinate will be persistent and transport will be essentially unretarded. The availability of alternative nitrogen sources was also indicated as a parameter that can affect persistence.

Measurement of stable isotope ratio of organic carbon in water samples

International Nuclear Information System (INIS)

Fujii, Toshihiro; Otsuki, Akira

1977-01-01

A new method for the measurement of stable isotope ratios was investigated and applied to organic carbon's isotope ratio measurements in water samples. A few river water samples from Tsuchiura city were tested. After the wet oxidation of organic carbons to carbon dioxide in a sealed ampoule, the isotope ratios were determined with the gas chromatograph-quadrupole mass spectrometer combined with a total organic carbon analyser, under the dynamic conditions. The GC-MS had been equipped with the multiple ion detector-digital integrator system. The ion intensities at m/e 44 and 45 were simultaneously measured at a switching rate of 1 ms. The measurements with carbon dioxide acquired from sodium carbonate (53 μg) gave the isotope ratios with the variation coefficient of 0.62%. However, the variation coefficients obtained from organic carbons in natural water samples were 2 to 3 times as high as that from sodium carbonate. This method is simple and rapid and may be applied to various fields especially in biology and medicine. (auth.)

Dry season limnological conditions and basin geology exhibit complex relationships with δ13C and δ15N of carbon sources in four Neotropical floodplains.

Science.gov (United States)

Zaia Alves, Gustavo H; Hoeinghaus, David J; Manetta, Gislaine I; Benedito, Evanilde

2017-01-01

Studies in freshwater ecosystems are seeking to improve understanding of carbon flow in food webs and stable isotopes have been influential in this work. However, variation in isotopic values of basal production sources could either be an asset or a hindrance depending on study objectives. We assessed the potential for basin geology and local limnological conditions to predict stable carbon and nitrogen isotope values of six carbon sources at multiple locations in four Neotropical floodplain ecosystems (Paraná, Pantanal, Araguaia, and Amazon). Limnological conditions exhibited greater variation within than among systems. δ15N differed among basins for most carbon sources, but δ13C did not (though high within-basin variability for periphyton, phytoplankton and particulate organic carbon was observed). Although δ13C and δ15N values exhibited significant correlations with some limnological factors within and among basins, those relationships differed among carbon sources. Regression trees for both carbon and nitrogen isotopes for all sources depicted complex and in some cases nested relationships, and only very limited similarity was observed among trees for different carbon sources. Although limnological conditions predicted variation in isotope values of carbon sources, we suggest the resulting models were too complex to enable mathematical corrections of source isotope values among sites based on these parameters. The importance of local conditions in determining variation in source isotope values suggest that isotopes may be useful for examining habitat use, dispersal and patch dynamics within heterogeneous floodplain ecosystems, but spatial variability in isotope values needs to be explicitly considered when testing ecosystem models of carbon flow in these systems.

Dynamics of carbon sources supporting burial in seagrass sediments under increasing anthropogenic pressure

KAUST Repository

Mazarrasa, Inés

2017-03-15

Seagrass meadows are strong coastal carbon sinks of autochthonous and allochthonous carbon. The aim of this study was to assess the effect of coastal anthropogenic pressure on the variability of carbon sources in seagrass carbon sinks during the last 150 yr. We did so by examining the composition of the sediment organic carbon (Corg) stocks by measuring the δ13Corg signature and C : N ratio in 210Pb dated sediments of 11 Posidonia oceanica seagrass meadows around the Balearic Islands (Spain, Western Mediterranean) under different levels of human pressure. On average, the top meter sediment carbon deposits were mainly (59% ± 12%) composed by P. oceanica derived carbon whereas seston contribution was generally lower (41% ± 8%). The contribution of P. oceanica to the total sediment carbon stock was the highest (∼ 80%) in the most pristine sites whereas the sestonic contribution was the highest (∼ 40–80%) in the meadows located in areas under moderate to very high human pressure. Furthermore, an increase in the contribution of sestonic carbon and a decrease in that of seagrass derived carbon toward present was observed in most of the meadows examined, coincident with the onset of the tourism industry development and coastal urbanization in the region. Our results demonstrate a general increase of total carbon accumulation rate in P. oceanica sediments during the last century, mainly driven by the increase in sestonic Corg carbon burial, which may have important implications in the long-term carbon sink capacity of the seagrass meadows in the region examined.

Utilization of carbon and nitrogen sources by Streptomyces ...

African Journals Online (AJOL)

We tested a number of carbon and nitrogen compounds for their effect on the production of an antibacterial antibiotic by Streptomyces kananmyceticus M27. Dextrose was found to be the most suitable carbon source, though maltose, sucrose, and soluble starch gave moderate yields. (NH4)H2PO4 and yeast extract were ...

Distribution of organic carbon in sediments from the Arabian Sea

Digital Repository Service at National Institute of Oceanography (India)

Paropkari, A.L.; Mascarenhas, A.; PrakashBabu, C.

Many earlier studies on the distribution of organic carbon in the Arabian Sea, sediments have projected contradictory opinions on the factors favouring accumulation and preservation of organic carbon in the Arabian Sea. An attempt is made...

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

International Nuclear Information System (INIS)

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 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 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

Analysis of Seasonal Soil Organic Carbon Content at Bukit Jeriau Forest, Fraser Hill, Pahang

International Nuclear Information System (INIS)

Ahmad Adnan Mohamed; Ahmad Adnan Mohamed; Sahibin Abd Rahim; David Allan Aitman; Mohd Khairul Amri Kamarudin; Mohd Khairul Amri Kamarudin

2016-01-01

Soil carbon is the carbon held within the soil, primarily in association with its organic content. The total soil organic carbon study was determined in a plot at Bukit Jeriau forest in Bukit Fraser, Pahang, Malaysia. The aim of this study is to determine the changing of soil organic carbon between wet season and dry season. Soil organic carbon was fined out using titrimetric determination. The soil organic carbon content in wet season is 223.24 t/ ha while dry season is 217.90 t/ ha. The soil pH range in wet season is between 4.32 to 4.45 and in dry season in 3.95 to 4.08 which is considered acidic. Correlation analysis showed that soil organic carbon value is influenced by pH value and climate. Correlation analysis between clay and soil organic carbon with depth showed positively significant differences and clay are very much influenced soil organic carbon content. Correlation analysis between electrical conductivity and soil organic carbon content showed negative significantly difference on wet season and positively significant different in dry season. (author)

Antibacterial Activity of Culture Extracts of Penicillium chrysogenum PCL501: Effects of Carbon Sources

Directory of Open Access Journals (Sweden)

Blessing M. Onyegeme-Okerenta

2009-05-01

Full Text Available Penicillium chrysogenum PCL501 produced β-lactam antibiotics when fermented with different agro-wastes: cassava shavings, corncob, sawdust and sugarcane pulp. In vitro antibacterial activity of the culture extracts was tested against four clinical bacterial isolates, namely, Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa. All the culture extracts and standard drug (commercial Benzyl Penicillin inhibited the growth B. subtilis and E. coli; the potency varied with carbon source. Antibacterial activity of extracts from cultures containing cassava shavings and sugarcane pulp was comparable with that of the standard drug. The MIC against the susceptible organisms was 0.20mg/ml for the standard drug and ranged from 0.40 to 1.50mg/ml for the culture extracts. Neither the culture extracts nor the standard drug inhibited K. pneumoniae and P. aeruginosa; the bacterial strains produced β-lactamase enzymes. Cassava shavings and sugarcane pulp are indicated as suitable cheap carbon sources for the production of antibiotics by Penicillium chrysogenum PCL501.

Assessing the potential of amino acid 13C patterns as a carbon source tracer in marine sediments: effects of algal growth conditions and sedimentary diagenesis

Science.gov (United States)

Larsen, T.; Bach, L. T.; Salvatteci, R.; Wang, Y. V.; Andersen, N.; Ventura, M.; McCarthy, M. D.

2015-08-01

Burial of organic carbon in marine sediments has a profound influence in marine biogeochemical cycles and provides a sink for greenhouse gases such as CO2 and CH4. However, tracing organic carbon from primary production sources as well as its transformations in the sediment record remains challenging. Here we examine a novel but growing tool for tracing the biosynthetic origin of amino acid carbon skeletons, based on naturally occurring stable carbon isotope patterns in individual amino acids (δ13CAA). We focus on two important aspects for δ13CAA utility in sedimentary paleoarchives: first, the fidelity of source diagnostic of algal δ13CAA patterns across different oceanographic growth conditions, and second, the ability of δ13CAA patterns to record the degree of subsequent microbial amino acid synthesis after sedimentary burial. Using the marine diatom Thalassiosira weissflogii, we tested under controlled conditions how δ13CAA patterns respond to changing environmental conditions, including light, salinity, temperature, and pH. Our findings show that while differing oceanic growth conditions can change macromolecular cellular composition, δ13CAA isotopic patterns remain largely invariant. These results emphasize that δ13CAA patterns should accurately record biosynthetic sources across widely disparate oceanographic conditions. We also explored how δ13CAA patterns change as a function of age, total nitrogen and organic carbon content after burial, in a marine sediment core from a coastal upwelling area off Peru. Based on the four most informative amino acids for distinguishing between diatom and bacterial sources (i.e., isoleucine, lysine, leucine and tyrosine), bacterially derived amino acids ranged from 10 to 15 % in the sediment layers from the last 5000 years, and up to 35 % during the last glacial period. The greater bacterial contributions in older sediments indicate that bacterial activity and amino acid resynthesis progressed, approximately as a

Carbon transfer from dissolved organic carbon to the cladoceran Bosmina: a mesocosm study

Directory of Open Access Journals (Sweden)

Tang Yali

2017-01-01

Full Text Available A mesocosm study illuminated possible transfer pathways for dissolved organic carbon from the water column to zooplankton. Organic carbon was added as 13C enriched glucose to 15 mesocosms filled with natural lake water. Stable isotope analysis and phospholipid fatty acids-based stable isotope probing were used to trace the incorporation of 13C into the cladoceran Bosmina and its potential food items. Glucose-C was shown to be assimilated into phytoplankton (including fungi and heterotrophic protists, bacteria and Bosmina, all of which became enriched with 13C during the experiment. The study suggests that bacteria play an important role in the transfer of glucose-C to Bosmina. Furthermore, osmotic algae, fungi and heterotrophic protists might also contribute to the isotopic signature changes observed in Bosmina. These findings help to clarify the contribution of dissolved organic carbon to zooplankton and its potential pathways.

Shunting arc plasma source for pure carbon ion beam

Energy Technology Data Exchange (ETDEWEB)

Koguchi, H.; Sakakita, H.; Kiyama, S.; Shimada, T.; Sato, Y.; Hirano, Y. [Energy Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba, Ibaraki 305-8568 (Japan)

2012-02-15

A plasma source is developed using a coaxial shunting arc plasma gun to extract a pure carbon ion beam. The pure carbon ion beam is a new type of deposition system for diamond and other carbon materials. Our plasma device generates pure carbon plasma from solid-state carbon material without using a hydrocarbon gas such as methane gas, and the plasma does not contain any hydrogen. The ion saturation current of the discharge measured by a double probe is about 0.2 mA/mm{sup 2} at the peak of the pulse.

Shunting arc plasma source for pure carbon ion beam.

Science.gov (United States)

Koguchi, H; Sakakita, H; Kiyama, S; Shimada, T; Sato, Y; Hirano, Y

2012-02-01

A plasma source is developed using a coaxial shunting arc plasma gun to extract a pure carbon ion beam. The pure carbon ion beam is a new type of deposition system for diamond and other carbon materials. Our plasma device generates pure carbon plasma from solid-state carbon material without using a hydrocarbon gas such as methane gas, and the plasma does not contain any hydrogen. The ion saturation current of the discharge measured by a double probe is about 0.2 mA∕mm(2) at the peak of the pulse.

Assessing the potential of amino acid δ13C patterns as a carbon source tracer in marine sediments: effects of algal growth conditions and sedimentary diagenesis

Science.gov (United States)

Larsen, T.; Bach, L. T.; Salvatteci, R.; Wang, Y. V.; Andersen, N.; Ventura, M.; McCarthy, M. D.

2015-01-01

Burial of organic carbon in marine sediments has a profound influence in marine biogeochemical cycles, and provides a sink for greenhouse gases such as CO2 and CH4. However, tracing organic carbon from primary production sources as well as its transformations in the sediment record remains challenging. Here we examine a novel but growing tool for tracing biosynthetic origin of amino acid carbon skeletons, based on natural occurring stable carbon isotope patterns in individual amino acids (δ13CAA). We focus on two important aspects for δ13CAA utility in sedimentary paleoarchives: first, the fidelity of source diagnostic of algal δ13CAA patterns across different oceanographic growth conditions; and second, the ability of δ13CAA patterns to record the degree of subsequent microbial amino acid synthesis after sedimentary burial. Using the marine diatom Thalassiosira weissflogii, we tested under controlled conditions how δ13CAA patterns respond to changing environmental conditions, including light, salinity, temperature, and pH. Our findings show that while differing oceanic growth conditions can change macromolecular cellular composition, δ13CAA isotopic patterns remain largely invariant. These results underscore that δ13CAA patterns should accurately record biosynthetic sources across widely disparate oceanographic conditions. We also explored how δ13CAA patterns change as a function of age, total nitrogen and organic carbon content after burial, in a marine sediment core from a coastal upwelling area off Peru. Based on the four most informative amino acids for distinguishing between diatom and bacterial sources (i.e. isoleucine, lysine, leucine and tyrosine), bacterial derived amino acids ranged from 10-15% in the sediment layers from the last 5000 years to 35% during the last glacial period. The larger bacterial fractions in older sediments indicate that bacterial activity and amino acid resynthesis progressed, approximately as a function of sediment age, to

Polycyclic aromatic hydrocarbons, elemental and organic carbon emissions from tire-wear.

Science.gov (United States)

Aatmeeyata; Sharma, Mukesh

2010-09-15

Tire-wear is an important source of PAHs, elemental carbon (EC) and organic carbon (OC). The emissions of these pollutants have been studied in an experimental set-up, simulating a realistic road-tire interaction (summer tire-concrete road). The large particle non-exhaust emissions (LPNE; diameter greater than 10 microm) have been evaluated over 14,500 km run of the tire. An increasing linear trend with cumulative km run was observed for emissions of PAHs and carbon. Amongst PAHs in LPNE, pyrene has been observed to be the highest (30+/-4 mg kg(-1)) followed by benzo[ghi]perylene (17+/-2 mg kg(-1)). Different fractions of EC-OC for tire-wear have been analyzed, and unlike exhaust emissions, EC1 was observed to be 99% of EC whereas more than 70% of the OC was the high temperature carbon (OC3 and OC4). The overall emission factors (mass tire(-1) km(-1)) for PAHs, EC and OC from tire-wear are 378 ng tire(-1) km(-1), 1.46 mg tire(-1) km(-1) and 2.37 mg tire(-1) km(-1) for small cars. Copyright 2010 Elsevier B.V. All rights reserved.

Physical and chemical protection of soil organic carbon in three agricultural soils with different contents of calcium carbonate

International Nuclear Information System (INIS)

Clough, A.; Skjemstad, J.O.

2000-01-01

The amount of organic carbon physically protected by entrapment within aggregates and through polyvalent cation organic matter bridging was determined on non-calcareous and calcareous soils. The composition of organic carbon in whole soils and 13 C NMR analysis. High energy photo-oxidation was carried out on <53 μm fractions and results from the NMR spectra showed 17-40% of organic carbon was in a condensed aromatic form, most likely charcoal (char). The concept that organic material remaining after photo-oxidation may be physically protected within aggregates was investigated by treating soils with a mild acid prior to photo-oxidation. More organic material was protected in the calcareous than the non-calcareous soils, regardless of whether the calcium occurred naturally or was an amendment. Acid treatment indicated that the presence of exchangeable calcium reduced losses of organic material upon photo-oxidation by about 7% due to calcium bridging. These results have implications for N fertiliser recommendations based upon organic carbon content. Firstly, calcium does not impact upon degradability of organic material to an extent likely to affect N fertiliser recommendations. Secondly, standard assessment techniques overestimate active organic carbon content in soils with high char content. Copyright (2000) CSIRO Publishing

Baseline map of organic carbon in Australian soil to support national carbon accounting and monitoring under climate change.

Science.gov (United States)

Viscarra Rossel, Raphael A; Webster, Richard; Bui, Elisabeth N; Baldock, Jeff A

2014-09-01

We can effectively monitor soil condition-and develop sound policies to offset the emissions of greenhouse gases-only with accurate data from which to define baselines. Currently, estimates of soil organic C for countries or continents are either unavailable or largely uncertain because they are derived from sparse data, with large gaps over many areas of the Earth. Here, we derive spatially explicit estimates, and their uncertainty, of the distribution and stock of organic C in the soil of Australia. We assembled and harmonized data from several sources to produce the most comprehensive set of data on the current stock of organic C in soil of the continent. Using them, we have produced a fine spatial resolution baseline map of organic C at the continental scale. We describe how we made it by combining the bootstrap, a decision tree with piecewise regression on environmental variables and geostatistical modelling of residuals. Values of stock were predicted at the nodes of a 3-arc-sec (approximately 90 m) grid and mapped together with their uncertainties. We then calculated baselines of soil organic C storage over the whole of Australia, its states and territories, and regions that define bioclimatic zones, vegetation classes and land use. The average amount of organic C in Australian topsoil is estimated to be 29.7 t ha(-1) with 95% confidence limits of 22.6 and 37.9 t ha(-1) . The total stock of organic C in the 0-30 cm layer of soil for the continent is 24.97 Gt with 95% confidence limits of 19.04 and 31.83 Gt. This represents approximately 3.5% of the total stock in the upper 30 cm of soil worldwide. Australia occupies 5.2% of the global land area, so the total organic C stock of Australian soil makes an important contribution to the global carbon cycle, and it provides a significant potential for sequestration. As the most reliable approximation of the stock of organic C in Australian soil in 2010, our estimates have important applications. They could support

Effect of carbon coating on cycle performance of LiFePO4/C composite cathodes using Tween80 as carbon source

International Nuclear Information System (INIS)

Huang, You-Guo; Zheng, Feng-Hua; Zhang, Xiao-Hui; Li, Qing-Yu; Wang, Hong-Qiang

2014-01-01

Highlights: • The Tween80 addition could enhance cycle stability of LiFePO 4 material. • The FTIR spectrum confirms Tween80 surfactant can bond with LiFePO 4 particles. • Some chemical bonds between material and carbon layer still exist after sintering. - Abstract: The influence of carbon coating on the cycle performance of LiFePO 4 /C composite cathodes using polyoxyethylenesorbitan monooleate (Tween80) as carbon source against lithium metal foil anode for Li-ion batteries was investigated in this paper. According to Infrared spectrum analysis (FTIR), the Tween80 surfactant molecules bond to the surface of LiFePO 4 and form an adsorption layer, which contribute to the formation of a homogeneous carbon layer tightly coating on the surface of LiFePO 4 particles in the process of sintering, due to a strong binding force provided by surface chemical bonds. The transmission electron microscopy (TEM) shows that the carbon layer around LiFePO 4 using Tween80 as carbon source still coating on the surface of LiFePO 4 after 200 cycles at 5 C rate while the carbon layer shed from the surface of LiFePO 4 using glucose as carbon source. As a result, the carbon-coated LiFePO 4 using Tween80 as carbon source exhibits much higher capacity retention than the sample using glucose as carbon source. Electrochemical impedance measurement (EIS) reveals that the carbon-coated LiFePO 4 electrode using Tween80 surfactant has a lower charge transfer resistance than the electrode using glucose as carbon source electrode after 100 and 200 cycles at 5 C rate

Organic Chemistry of Southern Sources: Microwave Spectroscopy of Cha-MMS1 and IRAS 15194-5115

Science.gov (United States)

Cordiner, Martin; Charnley, Steven

2011-01-01

We report new spectra of molecule-rich sources in the southern hemisphere obtained using the 22-meter Mopra telescope. Spectra and maps are presented of organic molecules detected between 30 and 50 GHz in the young Class 0 protostar Chamaeleon MMS-1. The large abundances of polyynes, cyanopolyynes and methanol may be indicative of a warm carbon chemistry in the dense gas surrounding this protostar. Spectra are also presented from a 78-96 GHz scan of the carbon-rich AGB star IRAS 15194-5115, including new detections of HC5N, CCS and C13CH.

Implication of using different carbon sources for denitrification in wastewater treatments.

Science.gov (United States)

Cherchi, Carla; Onnis-Hayden, Annalisa; El-Shawabkeh, Ibrahim; Gu, April Z

2009-08-01

Application of external carbon sources for denitrification becomes necessary for wastewater treatment plants that have to meet very stringent effluent nitrogen limits (e.g., 3 to 5 mgTN/L). In this study, we evaluated and compared three carbon sources--MicroC (Environmental Operating Solutions, Bourne, Massachusetts), methanol, and acetate-in terms of their denitrification rates and kinetics, effect on overall nitrogen removal performance, and microbial community structure of carbon-specific denitrifying enrichments. Denitrification rates and kinetics were determined with both acclimated and non-acclimated biomass, obtained from laboratory-scale sequencing batch reactor systems or full-scale plants. The results demonstrate the feasibility of the use of MicroC for denitrification processes, with maximum denitrification rates (k(dmax)) of 6.4 mgN/gVSSh and an observed yield of 0.36 mgVSS/mgCOD. Comparable maximum nitrate uptake rates were found with methanol, while acetate showed a maximum denitrification rate nearly twice as high as the others. The maximum growth rates measured at 20 degrees C for MicroC and methanol were 3.7 and 1.2 day(-1), respectively. The implications resulting from the differences in the denitrification rates and kinetics of different carbon sources on the full-scale nitrogen removal performance, under various configurations and operational conditions, were assessed using Biowin (EnviroSim Associates, Ltd., Flamborough, Ontario, Canada) simulations for both pre- and post-denitrification systems. Examination of microbial population structures using Automated Ribosomal Intergenic Spacer Analysis (ARISA) throughout the study period showed dynamic temporal changes and distinct microbial community structures of different carbon-specific denitrifying cultures. The ability of a specific carbon-acclimated denitrifying population to instantly use other carbon source also was investigated, and the chemical-structure-associated behavior patterns observed

Sediment source detection by stable isotope analysis, carbon and nitrogen content and CSSI in a small river of the Swiss Plateau

Science.gov (United States)

SchindlerWildhaber, Yael; Alewell, Christine; Birkholz, Axel

2014-05-01

Suspended sediment (SS) and organic matter in rivers can harm the fauna by affecting health and fitness of free swimming fish and by causing siltation of the riverbed. The temporal and spatial dynamics of sediment, carbon (C) and nitrogen (N) during the brown trout spawning season in a small river of the Swiss Plateau were assessed and C isotopes as well as the C/N atomic ratio were used to distinguish autochthonous and allochthonous sources of organic matter in SS loads. The visual basic program IsoSource with 13Ctot and 15N as input isotopes was used to quantify the temporal and spatial sources of SS. We determined compound specific stable carbon isotopes (CSSI) in fatty acids of possible sediment source areas to the stream in addition and compared them to SS from selected high flow and low flow events. Organic matter concentrations in the infiltrated and suspended sediment were highest during low flow periods with small sediment loads and lowest during high flow periods with high sediment loads. Peak values in nitrate and dissolved organic C were measured during high flow and high rainfall, probably due to leaching from pasture and arable land. The organic matter was of allochthonous sources as indicated by the C/N atomic ratio and δ13Corg. Organic matter in SS increased from up- to downstream due to an increase in sediment delivery from pasture and arable land downstream of the river. While the major sources of SS are pasture and arable land during base flow conditions, SS from forest soils increased during heavy rain events and warmer winter periods most likely due to snow melt which triggered erosion. Preliminary results of CSSI analysis of sediment source areas and comparison to SS of selected events indicate that differences in d13C values of individual fatty acids are too small to differentiate unambiguously between sediment sources.

Worldwide organic soil carbon and nitrogen data

Energy Technology Data Exchange (ETDEWEB)

Zinke, P.J.; Stangenberger, A.G. [Univ. of California, Berkeley, CA (United States). Dept. of Forestry and Resource Management; Post, W.M.; Emanual, W.R.; Olson, J.S. [Oak Ridge National Lab., TN (United States)

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.

Tracing Sources of Organic Matter in a Midwestern USA Reservoir using Online Tetramethylammonium Hydroxide (TMAH) Thermochemolysis

Science.gov (United States)

Hayes, J. M.; Blair, N. E.

2017-12-01

Increasingly industrial agriculture and food processing practices have created greater demand for water resources. In an attempt to meet this demand, many rivers have been dammed, however the resulting effects of the carbon cycle via carbon sequestration and methane production are not well understood. The organic geochemistry of sediment cores from Lake Decatur, IL, a 95-year-old impoundment on the Sangamon River in the Intensively Managed Landscape - Critical Zone Observatory (IML-CZO), was studied to assess the sources of organic matter to the lake. Online tetramethylammonium hydroxide (TMAH) thermochemolysis GC-MS was used to provide a broad-spectrum analysis using small samples with a minimum of preparation. Intensive corn and soy production have dominated Lake Decatur's nearly 2400 km2 watershed throughout its history. The agricultural land use has led to rapid soil erosion and infilling of the lake. Along with the eroded soil came organic matter enriched in 13C, which is attributed to corn, a C4 plant. This is consistent with an angiosperm-derived lignin signal, as indicated by high syringic/vanillic and cinnamic/vanillic lignin phenol ratios. Since approximately 1980, accumulating organic carbon has become increasingly 13C-depleted, indicating a change in organic carbon input to a more C3 plant signature. However, this is not due to a decrease in corn cultivation acreage, according to land use records. Instead, the ratio of algal (short chain, C12-C18) fatty acids to lignin increases correspondingly from this point, suggesting that this isotopic trend is the result of eutrophication in the lake due to agricultural fertilizer runoff. In the last decade, the organic carbon has become more 13C-enriched again, breaking the trend of the three previous decades. This inflection is captured in the return to a lower fatty acid to lignin ratio in the most recently deposited sediments. We speculate that this recent change in organic carbon input could be the result of

Validity of estimating the organic carbon content of basin sediment using color measurements

International Nuclear Information System (INIS)

Sasaki, Toshinori; Sugai, Toshihiko; Ogami, Takashi; Yanagida, Makoto; Yasue, Ken-ichi

2010-01-01

Psychometric lightness (L* value) measured by a colorimeter offers a rapid means of obtaining the organic carbon content of sediment. We measured peat and lacustrine sediments covering the past 300 ka - 106 samples for L* value and 197 samples for organic carbon content. L* values are highly correlated with organic carbon contents. Therefore, L* values are a convenient alternative to measuring organic carbon contents. (author)

Characterization of activated carbon produced from urban organic waste

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Abdul Gani Haji

2013-10-01

Full Text Available The difficulties to decompose organic waste can be handled naturally by pyrolisis so it can  decomposes quickly that produces charcoal as the product. This study aims to investigate the characteristics of activated carbon from urban organic waste. Charcoal results of pyrolysis of organic waste activated with KOH 1.0 M at a temperature of 700 and 800oC for 60 to 120 minutes. Characteristics of activated carbon were identified by Furrier Transform Infra Red (FTIR, Scanning Electron Microscopy (SEM, and X-Ray Diffraction (XRD. However, their quality is determined yield, moisture content, ash, fly substances, fixed carbon, and the power of adsorption of iodine and benzene. The identified functional groups on activated carbon, such as OH (3448,5-3436,9 cm-1, and C=O (1639,4 cm-1. In general, the degree and distance between the layers of active carbon crystallites produced activation in all treatments showed no significant difference. The pattern of activated carbon surface topography structure shows that the greater the pore formation in accordance with the temperature increase the more activation time needed. The yield of activated carbon obtained ranged from 72.04 to 82.75%. The results of characterization properties of activated carbon was obtained from 1.11 to 5.41% water, 13.68 to 17.27% substance fly, 20.36 to 26.59% ash, and 56.14 to 62.31% of fixed carbon . Absorption of activated carbon was good enough at 800oC and 120 minutes of activation time, that was equal to 409.52 mg/g of iodine and 14.03% of benzene. Activated carbon produced has less good quality, because only the water content and flying substances that meet the standards.Doi: 10.12777/ijse.5.2.89-94 [How to cite this article: Haji, A.G., Pari, G., Nazar, M., and Habibati.  (2013. Characterization of activated carbon produced from urban organic waste . International Journal of Science and Engineering, 5(2,89-94. Doi: 10.12777/ijse.5.2.89-94

Multiple sources driving the organic matter dynamics in two contrasting tropical mangroves

International Nuclear Information System (INIS)

Ray, R.; Shahraki, M.

2016-01-01

In this study, we have selected two different mangroves based on their geological, hydrological and climatological variations to investigate the origin (terrestrial, phytobenthos derived, and phytoplankton derived) of dissolved organic carbon (DOC), particulate organic carbon (POC) in the water column and the sedimentary OC using elemental ratios and stable isotopes. Qeshm Island, representing the Iranian mangroves received no attention before this study in terms of DOC, POC biogeochemistry and their sources unlike the Sundarbans (Indian side), the world's largest mangrove system. Slightly higher DOC concentrations in the Iranian mangroves were recorded in our field campaigns between 2011 and 2014, compared to the Sundarbans (315 ± 25 μM vs. 278 ± 42 μM), owing to the longer water residence times, while 9–10 times greater POC concentration (303 ± 37 μM, n = 82) was linked to both suspended load (345 ± 104 mg L"− "1) and high algal production. Yearlong phytoplankton bloom in the mangrove-lined Persian Gulf was reported to be the perennial source of both POC and DOC contributing 80–86% to the DOC and 90–98% to the POC pool. Whereas in the Sundarbans, riverine input contributed 50–58% to the DOC pool and POC composition was regulated by the seasonal litter fall, river discharge and phytoplankton production. Algal derived organic matter (microphytobenthos) represented the maximum contribution (70–76%) to the sedimentary OC at Qeshm Island, while mangrove leaf litters dominated the OC pool in the Indian Sundarbans. Finally, hydrographical settings (i.e. riverine transport) appeared to be the determinant factor in differentiating OM sources in the water column between the dry and wet mangroves. - Highlights: • Sources of OC have been identified and compared between two contrasting mangroves. • Phytoplankton dominated the DOC and POC pool in the Iranian mangroves. • River input contributed half of the total DOC and part of POC in the Indian

Multiple sources driving the organic matter dynamics in two contrasting tropical mangroves

Energy Technology Data Exchange (ETDEWEB)

Ray, R., E-mail: raghab.ray@gmail.com [Institut Universitaire Européen de la Mer, UBO, UMR 6539 LEMAR, rue Dumont dUrville, 29280 Plouzane (France); Leibniz Center for Tropical Marine Ecology, Fahrenheitstr. 6, 28359 Bremen (Germany); Shahraki, M. [Leibniz Center for Tropical Marine Ecology, Fahrenheitstr. 6, 28359 Bremen (Germany); Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research, Am Handelshafen 12, 27570 Bremerhaven (Germany)

2016-11-15

In this study, we have selected two different mangroves based on their geological, hydrological and climatological variations to investigate the origin (terrestrial, phytobenthos derived, and phytoplankton derived) of dissolved organic carbon (DOC), particulate organic carbon (POC) in the water column and the sedimentary OC using elemental ratios and stable isotopes. Qeshm Island, representing the Iranian mangroves received no attention before this study in terms of DOC, POC biogeochemistry and their sources unlike the Sundarbans (Indian side), the world's largest mangrove system. Slightly higher DOC concentrations in the Iranian mangroves were recorded in our field campaigns between 2011 and 2014, compared to the Sundarbans (315 ± 25 μM vs. 278 ± 42 μM), owing to the longer water residence times, while 9–10 times greater POC concentration (303 ± 37 μM, n = 82) was linked to both suspended load (345 ± 104 mg L{sup −} {sup 1}) and high algal production. Yearlong phytoplankton bloom in the mangrove-lined Persian Gulf was reported to be the perennial source of both POC and DOC contributing 80–86% to the DOC and 90–98% to the POC pool. Whereas in the Sundarbans, riverine input contributed 50–58% to the DOC pool and POC composition was regulated by the seasonal litter fall, river discharge and phytoplankton production. Algal derived organic matter (microphytobenthos) represented the maximum contribution (70–76%) to the sedimentary OC at Qeshm Island, while mangrove leaf litters dominated the OC pool in the Indian Sundarbans. Finally, hydrographical settings (i.e. riverine transport) appeared to be the determinant factor in differentiating OM sources in the water column between the dry and wet mangroves. - Highlights: • Sources of OC have been identified and compared between two contrasting mangroves. • Phytoplankton dominated the DOC and POC pool in the Iranian mangroves. • River input contributed half of the total DOC and part of POC in

Soil Organic Carbon assessment on two different forest management

Science.gov (United States)

Fernández Minguillón, Alex; Sauras Yera, Teresa; Vallejo Calzada, Ramón

2017-04-01

Soil Organic Carbon assessment on two different forest management. A.F. Minguillón1, T. Sauras1, V.R: Vallejo1. 1 Departamento de Biología Evolutiva, Ecología y Ciencias Ambientales, Universidad de Barcelona, Avenida Diagonal 643, 03080 Barcelona, Spain. Soils from arid and semiarid zones are characterized by a low organic matter content from scarce plant biomass and it has been proposed that these soils have a big capacity to carbon sequestration. According to IPCC ARS WG2 (2014) report and WG3 draft, increase carbon storage in terrestrial ecosystems has been identified such a potential tool for mitigation and adaptation to climate change. In ecological restoration context improve carbon sequestration is considered a management option with multiple benefits (win-win-win). Our work aims to analyze how the recently developed restoration techniques contributed to increases in terrestial ecosystem carbon storage. Two restoration techniques carried out in the last years have been evaluated. The study was carried out in 6 localities in Valencian Community (E Spain) and organic horizons of two different restoration techniques were evaluated; slash brush and thinning Aleppo pine stands. For each technique, carbon stock and its physical and chemical stability has been analysed. Preliminary results point out restoration zones acts as carbon sink due to (1) the relevant necromass input produced by slash brush increases C stock on the topsoil ;(2) Thinning increase carbon accumulation in vegetation.

Toward a quantitative and empirical dissolved organic carbon budget for the Gulf of Maine, a semienclosed shelf sea

Science.gov (United States)

Balch, William; Huntington, Thomas G.; Aiken, George R.; Drapeau, David; Bowler, Bruce; Lubelczyk, Laura; Butler, Kenna D.

2016-01-01

A time series of organic carbon export from Gulf of Maine (GoM) watersheds was compared to a time series of biological, chemical, bio-optical, and hydrographic properties, measured across the GoM between Yarmouth, NS, Canada, and Portland, ME, U.S. Optical proxies were used to quantify the dissolved organic carbon (DOC) and particulate organic carbon in the GoM. The Load Estimator regression model applied to river discharge data demonstrated that riverine DOC export (and its decadal variance) has increased over the last 80 years. Several extraordinarily wet years (2006–2010) resulted in a massive pulse of chromophoric dissolved organic matter (CDOM; proxy for DOC) into the western GoM along with unidentified optically scattering material (Time lags between DOC discharge and its appearance in the GoM increased with distance from the river mouths. Algae were also a significant source of DOC but not CDOM. Gulf-wide algal primary production has decreased. Increases in precipitation and DOC discharge to the GoM are predicted over the next century.

Input of particulate organic and dissolved inorganic carbon from the Amazon to the Atlantic Ocean

Science.gov (United States)

Druffel, E. R. M.; Bauer, J. E.; Griffin, S.

2005-03-01

We report concentrations and isotope measurements (radiocarbon and stable carbon) of dissolved inorganic carbon (DIC) and suspended particulate organic carbon (POC) in waters collected from the mouth of the Amazon River and the North Brazil Current. Samples were collected in November 1991, when the Amazon hydrograph was at its annual minimum and the North Brazil Current had retroflected into the equatorial North Atlantic. The DIC Δ14C results revealed postbomb carbon in river and ocean waters, with slightly higher values at the river mouth. The low DIC δ13C signature of the river end-member (-11‰) demonstrates that about half of the DIC originated from the remineralization of terrestrially derived organic matter. A linear relationship between DIC and salinity indicates that DIC was mixed nearly conservatively in the transition zone from the river mouth to the open ocean, though there was a small amount (≤10%) of organic matter remineralization in the mesohaline region. The POC Δ14C values in the river mouth were markedly lower than those values from the western Amazon region (Hedges et al., 1986). We conclude that the dominant source of POC near the river mouth and in the inner Amazon plume during November 1991 was aged, resuspended material of significant terrestrial character derived from shelf sediments, while the outer plume contained mainly marine-derived POC.

Leaching behavior of total organic carbon, nitrogen, and phosphorus from banana peel.

Science.gov (United States)

Jiang, Ruixue; Sun, Shujuan; Xu, Yan; Qiu, Xiudong; Yang, Jili; Li, Xiaochen

2015-01-01

The leaching behavior of organic carbon and nutrient compounds from banana peel (BP) was investigated in batch assays with respect to particle size, contact time, pH value, and temperature. The granularity, contact time, pH, and temperature caused no significant effects on the leaching of total phosphorus (TP) from the BP. The maximum leached total nitrogen (TN) content was found at pH 5.0 and 90 minutes, while no significant effects were caused by the granularity and temperature. The maximum leached total organic carbon (TOC) content was found by using a powder of 40 mesh, 150 minutes and at pH 6.0, while the temperature had no effect on the TOC leaching. The proportions of the TN, TP, and TOC contents leached from the dried BP ranged from 33.6% to 40.9%, 60.4% to 72.7%, and 8.2% to 9.9%, respectively, indicating that BP could be a potential pollution source for surface and ground water if discharged as domestic waste or reutilized without pretreatment.

A Precisely Assembled Carbon Source to Synthesize Fluorescent Carbon Quantum Dots for Sensing Probes and Bioimaging Agents.

Science.gov (United States)

Qiao, Yiqiang; Luo, Dan; Yu, Min; Zhang, Ting; Cao, Xuanping; Zhou, Yanheng; Liu, Yan

2018-02-09

A broad range of carbon sources have been used to fabricate varieties of carbon quantum dots (CQDs). However, the majority of these studies concern the influence of primary structures and chemical compositions of precursors on the CQDs; it is still unclear whether or not the superstructures of carbon sources have effects on the physiochemical properties of the synthetic CQDs. In this work, the concept of molecular assembly is first introduced into the design of a new carbon source. Compared with the tropocollagen molecules, the hierarchically assembled collagen scaffolds, as a new carbon source, immobilize functional groups of the precursors through hydrogen bonds, electrostatic attraction, and hydrophobic forces. Moreover, the accumulation of functional groups in collagen self-assembly further promotes the covalent bond formation in the obtained CQDs through a hydrothermal process. Both of these two chemical superiorities give rise to high quality CQDs with enhanced emission. The assembled collagen scaffold-based CQDs with heteroatom doping exhibit superior stability, and could be further applied as effective fluorescent probes for Fe 3+ detection and cellular cytosol imaging. These findings open a wealth of possibilities to explore more nanocarbons from precursors with assembled superstructures. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Carbon footprint of urban source separation for nutrient recovery.

Science.gov (United States)

Kjerstadius, H; Bernstad Saraiva, A; Spångberg, J; Davidsson, Å

2017-07-15

Source separation systems for the management of domestic wastewater and food waste has been suggested as more sustainable sanitation systems for urban areas. The present study used an attributional life cycle assessment to investigate the carbon footprint and potential for nutrient recovery of two sanitation systems for a hypothetical urban area in Southern Sweden. The systems represented a typical Swedish conventional system and a possible source separation system with increased nutrient recovery. The assessment included the management chain from household collection, transport, treatment and final return of nutrients to agriculture or disposal of the residuals. The results for carbon footprint and nutrient recovery (phosphorus and nitrogen) concluded that the source separation system could increase nutrient recovery (0.30-0.38 kg P capita -1 year -1 and 3.10-3.28 kg N capita -1 year -1 ), while decreasing the carbon footprint (-24 to -58 kg CO 2 -eq. capita -1 year -1 ), compared to the conventional system. The nutrient recovery was increased by the use of struvite precipitation and ammonium stripping at the wastewater treatment plant. The carbon footprint decreased, mainly due to the increased biogas production, increased replacement of mineral fertilizer in agriculture and less emissions of nitrous oxide from wastewater treatment. In conclusion, the study showed that source separation systems could potentially be used to increase nutrient recovery from urban areas, while decreasing the climate impact. Copyright © 2017 Elsevier Ltd. All rights reserved.

Nitrogen and carbon isotopes in soil with special reference to the diagnosis of organic matter

International Nuclear Information System (INIS)

Wada, Eitaro; Nakamura, Koichi.

1980-01-01

Distributions of nitrogen and carbon isotopes in terrestrial ecosystems are described based on available data and our recent findings for soil organic matters. Major processes regulating N-isotope and C-isotope ratios in biogenic substances are discussed. The biological di-nitrogen fixation and the precipitation are major sources which lower the delta 15 N value for forested soil organic matters. Denitrification enhances delta 15 N value for soil in cultivated fields. An addition of chemical fertilizer lowers 15 N content in soils. The permiation of soil water is an important factor controlling vertical profiles of delta 15 N in soil systems. Among soil organic matters, non-hydrolizable fraction seems to give unique low delta 15 N value, suggesting the utility of delta 15 N analysis in studying the nature of the fractions. delta 13 C of soil organic matter is significantly lower than that for marine sediments. delta 13 C for soil humus varies with respect to chemical forms as well as an age of soil organic matters. The variation is large in paddy fields. It is, thus, probable that delta 13 C is an useful parameter in studying the early epidiagenesis of soil organic matters. Based on the known delta 15 N-delta 13 C relationships, a two-source mixing model has been applied to assess sources of organic matters in coastal sediment. (author)